,species,ID,key,title,pub_year,Collected_year,Collected_location,lab_field,sex_1,sex_2,family.pair_1,family.pair_2,line.genotype.clone_1,line.genotype.clone_2,mother.dam_1,mother.dam_2,father.sire_1,father.sire_2,offspring.ind_1,offspring.ind_2,Statistics,Design,selection,narrow_broad,notedby,stage_1,stage_2,measure_1,measure_2,trait_1,trait_2,Include.exclude_reason,cov_cor,rG,var_rG,var_rG_type,Gvar_1,var_Gvar_1,var_Gvar_1_type,Gvar_2,var_Gvar_2,var_Gvar_2_type,Group,data_location,trait_rename_1,trait_rename_2,Design_rename,zr,n,sign,zr_sign,sex,stage,class,between
1,Acanthoscelides obtectus,262,rayyan-197247449,Genetic variation and covariation among life history traits in populations of Acanthoscelides obtectus maintained on different hosts,1997,NA,"Belgrade,Serbia",lab,female,female,NA,NA,NA,NA,300,300,75,75,1187,663,animal_model,full/half_sib,no,narrow,authors,non_adult,both,development time,female longevity,reverse_maturation,survival,include,cor,-0.575,NA,NA,NA,NA,NA,NA,NA,NA,variance_covariance_CB,table 5,maturation,survival,family,-0.654960691,300,-1,0.654960691,female,cross,Insecta,between
3,Acanthoscelides obtectus,262,rayyan-197247449,Genetic variation and covariation among life history traits in populations of Acanthoscelides obtectus maintained on different hosts,1997,NA,"Belgrade,Serbia",lab,female,female,NA,NA,NA,NA,300,300,75,75,663,663,animal_model,full/half_sib,no,narrow,authors,adult,both,fecundity,female longevity,fertility,survival,include,cor,0.036,NA,NA,NA,NA,NA,NA,NA,NA,variance_covariance_CB,table 5,fertility,survival,family,0.036015564,300,1,0.036015564,female,cross,Insecta,between
4,Acanthoscelides obtectus,262,rayyan-197247449,Genetic variation and covariation among life history traits in populations of Acanthoscelides obtectus maintained on different hosts,1997,NA,"Belgrade,Serbia",lab,female,female,NA,NA,NA,NA,300,300,75,75,693,693,animal_model,full/half_sib,no,narrow,authors,adult,both,fecundity,female longevity,fertility,survival,include,cor,-0.348,NA,NA,NA,NA,NA,NA,NA,NA,variance_covariance_CC,table 5,fertility,survival,family,-0.363166365,300,1,-0.363166365,female,cross,Insecta,between
6,Acanthoscelides obtectus,262,rayyan-197247449,Genetic variation and covariation among life history traits in populations of Acanthoscelides obtectus maintained on different hosts,1997,NA,"Belgrade,Serbia",lab,female,female,NA,NA,NA,NA,300,300,75,75,693,464,animal_model,full/half_sib,no,narrow,authors,non_adult,both,development time,female longevity,reverse_maturation,survival,include,cor,0.232,NA,NA,NA,NA,NA,NA,NA,NA,variance_covariance_PC,table 5,maturation,survival,family,0.236302205,300,-1,-0.236302205,female,cross,Insecta,between
7,Acanthoscelides obtectus,262,rayyan-197247449,Genetic variation and covariation among life history traits in populations of Acanthoscelides obtectus maintained on different hosts,1997,NA,"Belgrade,Serbia",lab,both,female,NA,NA,NA,NA,300,300,75,75,88,693,sire_mean_correlation,half_sib,no,broad,CC,non_adult,non_adult,egg-to-adult viability,development time,survival,reverse_maturation,include,cor,-0.028,NA,NA,NA,NA,NA,NA,NA,NA,sire_mean_PC,table 5,survival,maturation,family,-0.028007321,300,-1,0.028007321,female,non_adult,Insecta,between
8,Acanthoscelides obtectus,262,rayyan-197247449,Genetic variation and covariation among life history traits in populations of Acanthoscelides obtectus maintained on different hosts,1997,NA,"Belgrade,Serbia",lab,female,female,NA,NA,NA,NA,300,300,75,75,757,533,animal_model,full/half_sib,no,narrow,authors,non_adult,both,development time,female longevity,reverse_maturation,survival,include,cor,0.563,NA,NA,NA,NA,NA,NA,NA,NA,variance_covariance_PB,table 5,maturation,survival,family,0.637214568,300,-1,-0.637214568,female,cross,Insecta,between
10,Acanthoscelides obtectus,262,rayyan-197247449,Genetic variation and covariation among life history traits in populations of Acanthoscelides obtectus maintained on different hosts,1997,NA,"Belgrade,Serbia",lab,female,female,NA,NA,NA,NA,300,300,75,75,1103,693,animal_model,full/half_sib,no,narrow,authors,non_adult,both,development time,female longevity,reverse_maturation,survival,include,cor,-0.566,NA,NA,NA,NA,NA,NA,NA,NA,variance_covariance_CC,table 5,maturation,survival,family,-0.641617671,300,-1,0.641617671,female,cross,Insecta,between
13,Acanthoscelides obtectus,262,rayyan-197247449,Genetic variation and covariation among life history traits in populations of Acanthoscelides obtectus maintained on different hosts,1997,NA,"Belgrade,Serbia",lab,female,female,NA,NA,NA,NA,300,300,75,75,464,464,animal_model,full/half_sib,no,narrow,authors,adult,both,fecundity,female longevity,fertility,survival,include,cor,-0.086,NA,NA,NA,NA,NA,NA,NA,NA,variance_covariance_PC,table 5,fertility,survival,family,-0.086212965,300,1,-0.086212965,female,cross,Insecta,between
14,Acanthoscelides obtectus,262,rayyan-197247449,Genetic variation and covariation among life history traits in populations of Acanthoscelides obtectus maintained on different hosts,1997,NA,"Belgrade,Serbia",lab,female,female,NA,NA,NA,NA,300,300,75,75,1103,693,animal_model,full/half_sib,no,narrow,authors,non_adult,adult,development time,fecundity,reverse_maturation,fertility,include,cor,NA,NA,NA,NA,NA,NA,NA,NA,NA,variance_covariance_CC,table 5,maturation,fertility,family,NA,300,-1,NA,female,cross,Insecta,between
15,Acanthoscelides obtectus,262,rayyan-197247449,Genetic variation and covariation among life history traits in populations of Acanthoscelides obtectus maintained on different hosts,1997,NA,"Belgrade,Serbia",lab,both,female,NA,NA,NA,NA,300,300,75,75,88,464,sire_mean_correlation,half_sib,no,broad,CC,non_adult,adult,egg-to-adult viability,fecundity,survival,fertility,include,cor,-0.06,NA,NA,NA,NA,NA,NA,NA,NA,sire_mean_PC,table 5,survival,fertility,family,-0.060072156,300,1,-0.060072156,female,cross,Insecta,between
16,Acanthoscelides obtectus,262,rayyan-197247449,Genetic variation and covariation among life history traits in populations of Acanthoscelides obtectus maintained on different hosts,1997,NA,"Belgrade,Serbia",lab,both,female,NA,NA,NA,NA,300,300,75,75,129,663,sire_mean_correlation,half_sib,no,broad,CC,non_adult,adult,egg-to-adult viability,fecundity,survival,fertility,include,cor,-0.292,NA,NA,NA,NA,NA,NA,NA,NA,sire_mean_CB,table 5,survival,fertility,family,-0.300751295,300,1,-0.300751295,female,cross,Insecta,between
17,Acanthoscelides obtectus,262,rayyan-197247449,Genetic variation and covariation among life history traits in populations of Acanthoscelides obtectus maintained on different hosts,1997,NA,"Belgrade,Serbia",lab,both,female,NA,NA,NA,NA,300,300,75,75,126,693,sire_mean_correlation,half_sib,no,broad,CC,non_adult,adult,egg-to-adult viability,fecundity,survival,fertility,include,cor,-0.395,NA,NA,NA,NA,NA,NA,NA,NA,sire_mean_CC,table 5,survival,fertility,family,-0.417710618,300,1,-0.417710618,female,cross,Insecta,between
19,Acanthoscelides obtectus,262,rayyan-197247449,Genetic variation and covariation among life history traits in populations of Acanthoscelides obtectus maintained on different hosts,1997,NA,"Belgrade,Serbia",lab,both,female,NA,NA,NA,NA,300,300,75,75,88,757,sire_mean_correlation,half_sib,no,broad,CC,non_adult,non_adult,egg-to-adult viability,development time,survival,reverse_maturation,include,cor,-0.146,NA,NA,NA,NA,NA,NA,NA,NA,sire_mean_PB,table 5,survival,maturation,family,-0.147050852,300,-1,0.147050852,female,non_adult,Insecta,between
20,Acanthoscelides obtectus,262,rayyan-197247449,Genetic variation and covariation among life history traits in populations of Acanthoscelides obtectus maintained on different hosts,1997,NA,"Belgrade,Serbia",lab,female,female,NA,NA,NA,NA,300,300,75,75,1187,663,animal_model,full/half_sib,no,narrow,authors,non_adult,adult,development time,fecundity,reverse_maturation,fertility,include,cor,0.668,NA,NA,NA,NA,NA,NA,NA,NA,variance_covariance_CB,table 5,maturation,fertility,family,0.807122807,300,-1,-0.807122807,female,cross,Insecta,between
23,Acanthoscelides obtectus,262,rayyan-197247449,Genetic variation and covariation among life history traits in populations of Acanthoscelides obtectus maintained on different hosts,1997,NA,"Belgrade,Serbia",lab,female,female,NA,NA,NA,NA,300,300,75,75,757,533,animal_model,full/half_sib,no,narrow,authors,non_adult,adult,development time,fecundity,reverse_maturation,fertility,include,cor,-0.207,NA,NA,NA,NA,NA,NA,NA,NA,variance_covariance_PB,table 5,maturation,fertility,family,-0.210035,300,-1,0.210035,female,cross,Insecta,between
24,Acanthoscelides obtectus,262,rayyan-197247449,Genetic variation and covariation among life history traits in populations of Acanthoscelides obtectus maintained on different hosts,1997,NA,"Belgrade,Serbia",lab,both,female,NA,NA,NA,NA,300,300,75,75,129,1187,sire_mean_correlation,half_sib,no,broad,CC,non_adult,non_adult,egg-to-adult viability,development time,survival,reverse_maturation,include,cor,0.093,NA,NA,NA,NA,NA,NA,NA,NA,sire_mean_CB,table 5,survival,maturation,family,0.093269519,300,-1,-0.093269519,female,non_adult,Insecta,between
25,Acanthoscelides obtectus,262,rayyan-197247449,Genetic variation and covariation among life history traits in populations of Acanthoscelides obtectus maintained on different hosts,1997,NA,"Belgrade,Serbia",lab,both,female,NA,NA,NA,NA,300,300,75,75,126,1103,sire_mean_correlation,half_sib,no,broad,CC,non_adult,non_adult,egg-to-adult viability,development time,survival,reverse_maturation,include,cor,0.048,NA,NA,NA,NA,NA,NA,NA,NA,sire_mean_CC,table 5,survival,maturation,family,0.048036915,300,-1,-0.048036915,female,non_adult,Insecta,between
26,Acanthoscelides obtectus,262,rayyan-197247449,Genetic variation and covariation among life history traits in populations of Acanthoscelides obtectus maintained on different hosts,1997,NA,"Belgrade,Serbia",lab,female,female,NA,NA,NA,NA,300,300,75,75,693,464,animal_model,full/half_sib,no,narrow,authors,non_adult,adult,development time,fecundity,reverse_maturation,fertility,include,cor,0.357,NA,NA,NA,NA,NA,NA,NA,NA,variance_covariance_PC,table 5,maturation,fertility,family,0.373443468,300,-1,-0.373443468,female,cross,Insecta,between
27,Acanthoscelides obtectus,262,rayyan-197247449,Genetic variation and covariation among life history traits in populations of Acanthoscelides obtectus maintained on different hosts,1997,NA,"Belgrade,Serbia",lab,female,female,NA,NA,NA,NA,300,300,75,75,533,533,animal_model,full/half_sib,no,narrow,authors,adult,both,fecundity,female longevity,fertility,survival,include,cor,-0.493,NA,NA,NA,NA,NA,NA,NA,NA,variance_covariance_PB,table 5,fertility,survival,family,-0.540015897,300,1,-0.540015897,female,cross,Insecta,between
29,Acanthoscelides obtectus,262,rayyan-197247449,Genetic variation and covariation among life history traits in populations of Acanthoscelides obtectus maintained on different hosts,1997,NA,"Belgrade,Serbia",lab,both,female,NA,NA,NA,NA,300,300,75,75,88,533,sire_mean_correlation,half_sib,no,broad,CC,non_adult,adult,egg-to-adult viability,fecundity,survival,fertility,include,cor,0.009,NA,NA,NA,NA,NA,NA,NA,NA,sire_mean_PB,table 5,survival,fertility,family,0.009000243,300,1,0.009000243,female,cross,Insecta,between
31,Acanthoscelides obtectus,262,rayyan-197247449,Genetic variation and covariation among life history traits in populations of Acanthoscelides obtectus maintained on different hosts,1997,NA,"Belgrade,Serbia",lab,both,female,NA,NA,NA,NA,300,300,75,75,88,464,sire_mean_correlation,half_sib,no,broad,CC,non_adult,both,egg-to-adult viability,female longevity,survival,survival,include,cor,-0.307,NA,NA,NA,NA,NA,NA,NA,NA,sire_mean_PC,table 5,survival,survival,family,-0.317229857,300,1,-0.317229857,female,cross,Insecta,within
34,Acanthoscelides obtectus,262,rayyan-197247449,Genetic variation and covariation among life history traits in populations of Acanthoscelides obtectus maintained on different hosts,1997,NA,"Belgrade,Serbia",lab,both,female,NA,NA,NA,NA,300,300,75,75,88,533,sire_mean_correlation,half_sib,no,broad,CC,non_adult,both,egg-to-adult viability,female longevity,survival,survival,include,cor,0.095,NA,NA,NA,NA,NA,NA,NA,NA,sire_mean_PB,table 5,survival,survival,family,0.095287349,300,1,0.095287349,female,cross,Insecta,within
35,Acanthoscelides obtectus,262,rayyan-197247449,Genetic variation and covariation among life history traits in populations of Acanthoscelides obtectus maintained on different hosts,1997,NA,"Belgrade,Serbia",lab,both,female,NA,NA,NA,NA,300,300,75,75,129,663,sire_mean_correlation,half_sib,no,broad,CC,non_adult,both,egg-to-adult viability,female longevity,survival,survival,include,cor,0.493,NA,NA,NA,NA,NA,NA,NA,NA,sire_mean_CB,table 5,survival,survival,family,0.540015897,300,1,0.540015897,female,cross,Insecta,within
36,Acanthoscelides obtectus,262,rayyan-197247449,Genetic variation and covariation among life history traits in populations of Acanthoscelides obtectus maintained on different hosts,1997,NA,"Belgrade,Serbia",lab,both,female,NA,NA,NA,NA,300,300,75,75,126,693,sire_mean_correlation,half_sib,no,broad,CC,non_adult,both,egg-to-adult viability,female longevity,survival,survival,include,cor,0.182,NA,NA,NA,NA,NA,NA,NA,NA,sire_mean_CC,table 5,survival,survival,family,0.184050431,300,1,0.184050431,female,cross,Insecta,within
37,Acrobeloides nanus,210,rayyan-197247275,Rapid divergence of genetic variance-covariance matrix within a natural population,2008,NA,"Wageningen, Netherlands",lab,female,female,NA,NA,55,55,NA,NA,NA,NA,242,242,animal_model,genetic_line,no,broad,authors,adult,adult,total reproduction,reproductive period,fertility,fertility,include,cor,0.82,0.25,se,NA,NA,NA,NA,NA,NA,habitat_s,table 2,fertility,fertility,genotype,1.156817465,55,1,1.156817465,female,adult,Chromadorea,within
38,Acrobeloides nanus,210,rayyan-197247275,Rapid divergence of genetic variance-covariance matrix within a natural population,2008,NA,"Wageningen, Netherlands",lab,female,female,NA,NA,47,47,NA,NA,NA,NA,186,186,animal_model,genetic_line,no,broad,authors,both,adult,lifespan,reproductive period,survival,fertility,include,cor,0.4,3.6,se,NA,NA,NA,NA,NA,NA,habitat_b,table 2,survival,fertility,genotype,0.42364893,47,1,0.42364893,female,cross,Chromadorea,between
39,Acrobeloides nanus,210,rayyan-197247275,Rapid divergence of genetic variance-covariance matrix within a natural population,2008,NA,"Wageningen, Netherlands",lab,female,female,NA,NA,55,55,NA,NA,NA,NA,242,242,animal_model,genetic_line,no,broad,authors,both,adult,lifespan,reproductive period,survival,fertility,include,cor,0.98,0.82,se,NA,NA,NA,NA,NA,NA,habitat_s,table 2,survival,fertility,genotype,2.297559925,55,1,2.297559925,female,cross,Chromadorea,between
40,Acrobeloides nanus,210,rayyan-197247275,Rapid divergence of genetic variance-covariance matrix within a natural population,2008,NA,"Wageningen, Netherlands",lab,female,female,NA,NA,55,55,NA,NA,NA,NA,242,242,animal_model,genetic_line,no,broad,authors,adult,both,total reproduction,lifespan,fertility,survival,include,cor,0.92,0.91,se,NA,NA,NA,NA,NA,NA,habitat_s,table 2,fertility,survival,genotype,1.589026915,55,1,1.589026915,female,cross,Chromadorea,between
41,Acrobeloides nanus,210,rayyan-197247275,Rapid divergence of genetic variance-covariance matrix within a natural population,2008,NA,"Wageningen, Netherlands",lab,female,female,NA,NA,47,47,NA,NA,NA,NA,186,186,animal_model,genetic_line,no,broad,authors,adult,both,total reproduction,lifespan,fertility,survival,include,cor,-0.24,1.16,se,NA,NA,NA,NA,NA,NA,habitat_b,table 2,fertility,survival,genotype,-0.244774113,47,1,-0.244774113,female,cross,Chromadorea,between
42,Acrobeloides nanus,210,rayyan-197247275,Rapid divergence of genetic variance-covariance matrix within a natural population,2008,NA,"Wageningen, Netherlands",lab,female,female,NA,NA,47,47,NA,NA,NA,NA,186,186,animal_model,genetic_line,no,broad,authors,adult,adult,total reproduction,reproductive period,fertility,fertility,include,cor,0.44,0.73,se,NA,NA,NA,NA,NA,NA,habitat_b,table 2,fertility,fertility,genotype,0.472230804,47,1,0.472230804,female,adult,Chromadorea,within
43,Amauronematus amplus,397,rayyan-697473009,Seasonally varying diet quality and the quantitative genetics of development time and body size in birch feeding insects,2001,NA,Finland,lab,male,male,NA,NA,NA,NA,23,23,NA,NA,358,358,animal_model,full_sib,no,broad,authors,non_adult,non_adult,development time,final larval mass,reverse_maturation,size,include,cor,0.169,0.308,se,NA,NA,NA,NA,NA,NA,species_2_covariance,figure 2a,maturation,size,family,0.170637083,23,-1,-0.170637083,male,non_adult,Insecta,between
45,Ambystoma macrodactylum columbianum,100,rayyan-697471781,Genetic covariance structure of growth in the salamander Ambystoma macrodactylum,2004,2000,"Whitman County, Washington",lab,both,both,13,13,NA,NA,13,13,13,13,113,113,animal_model,full_sib,no,broad,authors,adult,non_adult,SVL at metamorphosis,age at metamorphosis,size,reverse_maturation,include,cor,0.471,0.0319,se,NA,NA,NA,NA,NA,NA,rayyan-697471781,last para in result,size,maturation,family,0.511354644,13,-1,-0.511354644,both,cross,Amphibia,between
46,Ambystoma macrodactylum columbianum,100,rayyan-697471781,Genetic covariance structure of growth in the salamander Ambystoma macrodactylum,2004,2000,"Whitman County, Washington",lab,both,both,13,13,NA,NA,13,13,13,13,113,113,animal_model,full_sib,no,broad,authors,adult,non_adult,mass at metamorphosis,age at metamorphosis,size,reverse_maturation,include,cor,0.749,0.165,se,NA,NA,NA,NA,NA,NA,rayyan-697471781,last para in result,size,maturation,family,0.970673268,13,-1,-0.970673268,both,cross,Amphibia,between
48,Anopheles gambiae,388,rayyan-697472961,"Genetic contribution to variation in larval development time, adult size, and longevity of starved adults of Anopheles gambiae",2006,2003,"Bobo Dioulasso, Burkina Faso",lab,male,male,27,27,NA,NA,NA,NA,NA,NA,545,545,family_mean_correlation,full_sib,no,broad,authors,non_adult,both,development time,adult longevity,reverse_maturation,survival,include,cor,-0.4,NA,NA,NA,NA,NA,NA,NA,NA,male_all,table 1,maturation,survival,family,-0.42364893,27,-1,0.42364893,male,cross,Insecta,between
51,Anopheles gambiae,388,rayyan-697472961,"Genetic contribution to variation in larval development time, adult size, and longevity of starved adults of Anopheles gambiae",2006,2003,"Bobo Dioulasso, Burkina Faso",lab,male,male,27,27,NA,NA,NA,NA,NA,NA,545,545,family_mean_correlation,full_sib,no,broad,authors,non_adult,adult,development time,adult dry wight,reverse_maturation,size,include,cor,-0.47,NA,NA,NA,NA,NA,NA,NA,NA,male_all,table 1,maturation,size,family,-0.510070337,27,-1,0.510070337,male,cross,Insecta,between
54,Anopheles gambiae,388,rayyan-697472961,"Genetic contribution to variation in larval development time, adult size, and longevity of starved adults of Anopheles gambiae",2006,2003,"Bobo Dioulasso, Burkina Faso",lab,female,female,27,27,NA,NA,NA,NA,NA,NA,625,625,family_mean_correlation,full_sib,no,broad,authors,both,adult,adult longevity,adult dry wight,survival,size,include,cor,0.56,NA,NA,NA,NA,NA,NA,NA,NA,female_all,table 1,survival,size,family,0.632833187,27,1,0.632833187,female,cross,Insecta,between
57,Anopheles gambiae,388,rayyan-697472961,"Genetic contribution to variation in larval development time, adult size, and longevity of starved adults of Anopheles gambiae",2006,2003,"Bobo Dioulasso, Burkina Faso",lab,female,female,27,27,NA,NA,NA,NA,NA,NA,625,625,family_mean_correlation,full_sib,no,broad,authors,non_adult,adult,development time,adult dry wight,reverse_maturation,size,include,cor,-0.5,NA,NA,NA,NA,NA,NA,NA,NA,female_all,table 1,maturation,size,family,-0.549306144,27,-1,0.549306144,female,cross,Insecta,between
59,Anopheles gambiae,388,rayyan-697472961,"Genetic contribution to variation in larval development time, adult size, and longevity of starved adults of Anopheles gambiae",2006,2003,"Bobo Dioulasso, Burkina Faso",lab,female,female,27,27,NA,NA,NA,NA,NA,NA,625,625,family_mean_correlation,full_sib,no,broad,authors,non_adult,both,development time,adult longevity,reverse_maturation,survival,include,cor,-0.56,NA,NA,NA,NA,NA,NA,NA,NA,female_all,table 1,maturation,survival,family,-0.632833187,27,-1,0.632833187,female,cross,Insecta,between
62,Anopheles gambiae,388,rayyan-697472961,"Genetic contribution to variation in larval development time, adult size, and longevity of starved adults of Anopheles gambiae",2006,2003,"Bobo Dioulasso, Burkina Faso",lab,male,male,27,27,NA,NA,NA,NA,NA,NA,545,545,family_mean_correlation,full_sib,no,broad,authors,both,adult,adult longevity,adult dry wight,survival,size,include,cor,0.48,NA,NA,NA,NA,NA,NA,NA,NA,male_all,table 1,survival,size,family,0.522984278,27,1,0.522984278,male,cross,Insecta,between
69,Aphis fabae,94,rayyan-697471756,Phenotypic plasticity in host-plant specialisation in Aphis fabae,2005,NA,"Colchester,Essex, U.K.",lab,both,both,NA,NA,13,13,NA,NA,NA,NA,65,65,line_mean_correlation,genetic_line,no,broad,CC,non_adult,adult,development rate,relative fecundity (number of offspring produced per day),maturation,fertility,include,cor,0.53,"[0.03, 0.83]",95CI,NA,NA,NA,NA,NA,NA,nasturtium,table 2,maturation,fertility,genotype,0.59014516,13,1,0.59014516,both,cross,Insecta,between
70,Aphis fabae,94,rayyan-697471756,Phenotypic plasticity in host-plant specialisation in Aphis fabae,2005,NA,"Colchester,Essex, U.K.",lab,both,both,NA,NA,13,13,NA,NA,NA,NA,65,65,line_mean_correlation,genetic_line,no,broad,CC,non_adult,non_adult,development rate,relative growth rate,maturation,growth,include,cor,0.81,"[0.46, 0.94]",95CI,NA,NA,NA,NA,NA,NA,broad_bean,table 2,maturation,growth,genotype,1.127029026,13,1,1.127029026,both,non_adult,Insecta,between
71,Aphis fabae,94,rayyan-697471756,Phenotypic plasticity in host-plant specialisation in Aphis fabae,2005,NA,"Colchester,Essex, U.K.",lab,both,both,NA,NA,13,13,NA,NA,NA,NA,65,65,line_mean_correlation,genetic_line,no,broad,CC,adult,non_adult,adult weight,relative growth rate,size,growth,include,cor,0.76,"[0.35, 0.93]",95CI,NA,NA,NA,NA,NA,NA,broad_bean,table 2,size,growth,genotype,0.996215082,13,1,0.996215082,both,cross,Insecta,between
72,Aphis fabae,94,rayyan-697471756,Phenotypic plasticity in host-plant specialisation in Aphis fabae,2005,NA,"Colchester,Essex, U.K.",lab,both,both,NA,NA,13,13,NA,NA,NA,NA,65,65,line_mean_correlation,genetic_line,no,broad,CC,non_adult,adult,development rate,relative fecundity (number of offspring produced per day),maturation,fertility,include,cor,0.94,"[0.80, 0.98]",95CI,NA,NA,NA,NA,NA,NA,broad_bean,table 2,maturation,fertility,genotype,1.738049345,13,1,1.738049345,both,cross,Insecta,between
73,Aphis fabae,94,rayyan-697471756,Phenotypic plasticity in host-plant specialisation in Aphis fabae,2005,NA,"Colchester,Essex, U.K.",lab,both,both,NA,NA,13,13,NA,NA,NA,NA,65,65,line_mean_correlation,genetic_line,no,broad,CC,adult,non_adult,adult weight,relative growth rate,size,growth,include,cor,0.6,"[0.07, 0.87]",95CI,NA,NA,NA,NA,NA,NA,nasturtium,table 2,size,growth,genotype,0.693147181,13,1,0.693147181,both,cross,Insecta,between
74,Aphis fabae,285,rayyan-197247748,Variation and covariation of life history traits in aphids are related to infection with the facultative bacterial endosymbiont Hamiltonella defensa,2010,2006,Switzerland,lab,female,female,NA,NA,21,21,NA,NA,NA,NA,147,147,line_mean_correlation,genetic_line,no,broad,CC,non_adult,adult,development time,offspring production,reverse_maturation,fertility,include,cor,-0.58,0.19,se,NA,NA,NA,NA,NA,NA,all,table 3,maturation,fertility,genotype,-0.662462707,21,-1,0.662462707,female,cross,Insecta,between
75,Aphis fabae,94,rayyan-697471756,Phenotypic plasticity in host-plant specialisation in Aphis fabae,2005,NA,"Colchester,Essex, U.K.",lab,both,both,NA,NA,13,13,NA,NA,NA,NA,65,65,line_mean_correlation,genetic_line,no,broad,CC,non_adult,non_adult,development rate,relative growth rate,maturation,growth,include,cor,0.84,"[0.53, 0.95]",95CI,NA,NA,NA,NA,NA,NA,nasturtium,table 2,maturation,growth,genotype,1.221173518,13,1,1.221173518,both,non_adult,Insecta,between
79,Aphis fabae,285,rayyan-197247748,Variation and covariation of life history traits in aphids are related to infection with the facultative bacterial endosymbiont Hamiltonella defensa,2010,2006,Switzerland,lab,female,female,NA,NA,21,21,NA,NA,NA,NA,147,147,line_mean_correlation,genetic_line,no,broad,CC,adult,non_adult,offspring production,newborn offspring body size,fertility,size,include,cor,0.26,0.22,se,NA,NA,NA,NA,NA,NA,all,table 3,fertility,size,genotype,0.266108407,21,1,0.266108407,female,cross,Insecta,between
84,Aphis fabae,285,rayyan-197247748,Variation and covariation of life history traits in aphids are related to infection with the facultative bacterial endosymbiont Hamiltonella defensa,2010,2006,Switzerland,lab,female,female,NA,NA,21,21,NA,NA,NA,NA,147,147,line_mean_correlation,genetic_line,no,broad,CC,adult,adult,adult female body mass at maturity,offspring production,size,fertility,include,cor,0.51,0.2,se,NA,NA,NA,NA,NA,NA,all,table 3,size,fertility,genotype,0.562729769,21,1,0.562729769,female,adult,Insecta,between
86,Aphis fabae,94,rayyan-697471756,Phenotypic plasticity in host-plant specialisation in Aphis fabae,2005,NA,"Colchester,Essex, U.K.",lab,both,both,NA,NA,13,13,NA,NA,NA,NA,65,65,line_mean_correlation,genetic_line,no,broad,CC,adult,non_adult,relative fecundity (number of offspring produced per day),relative growth rate,fertility,growth,include,cor,0.83,"[0.51, 0.95]",95CI,NA,NA,NA,NA,NA,NA,broad_bean,table 2,fertility,growth,genotype,1.188136404,13,1,1.188136404,both,cross,Insecta,between
88,Aphis fabae,285,rayyan-197247748,Variation and covariation of life history traits in aphids are related to infection with the facultative bacterial endosymbiont Hamiltonella defensa,2010,2006,Switzerland,lab,female,female,NA,NA,21,21,NA,NA,NA,NA,147,147,line_mean_correlation,genetic_line,no,broad,CC,adult,non_adult,adult female body mass at maturity,newborn offspring body size,size,size,include,cor,0.65,0.7,se,NA,NA,NA,NA,NA,NA,all,table 3,size,size,genotype,0.775298706,21,1,0.775298706,female,cross,Insecta,within
90,Aphis fabae,94,rayyan-697471756,Phenotypic plasticity in host-plant specialisation in Aphis fabae,2005,NA,"Colchester,Essex, U.K.",lab,both,both,NA,NA,13,13,NA,NA,NA,NA,65,65,line_mean_correlation,genetic_line,no,broad,CC,adult,non_adult,adult weight,1/development time,size,maturation,include,cor,0.42,"[0.18, 0.78]",95CI,NA,NA,NA,NA,NA,NA,nasturtium,table 2,size,maturation,genotype,0.447692024,13,1,0.447692024,both,cross,Insecta,between
92,Aphis fabae,94,rayyan-697471756,Phenotypic plasticity in host-plant specialisation in Aphis fabae,2005,NA,"Colchester,Essex, U.K.",lab,both,both,NA,NA,13,13,NA,NA,NA,NA,65,65,line_mean_correlation,genetic_line,no,broad,CC,non_adult,adult,birth weight,adult weight,size,size,include,cor,0.55,"[-0.66, 0.85]",95CI,NA,NA,NA,NA,NA,NA,broad_bean,table 2,size,size,genotype,0.618381314,13,1,0.618381314,both,cross,Insecta,within
93,Aphis fabae,94,rayyan-697471756,Phenotypic plasticity in host-plant specialisation in Aphis fabae,2005,NA,"Colchester,Essex, U.K.",lab,both,both,NA,NA,13,13,NA,NA,NA,NA,65,65,line_mean_correlation,genetic_line,no,broad,CC,adult,adult,adult weight,relative fecundity (number of offspring produced per day),size,fertility,include,cor,0.77,"[0.36, 0.96]",95CI,NA,NA,NA,NA,NA,NA,nasturtium,table 2,size,fertility,genotype,1.020327758,13,1,1.020327758,both,adult,Insecta,between
95,Aphis fabae,94,rayyan-697471756,Phenotypic plasticity in host-plant specialisation in Aphis fabae,2005,NA,"Colchester,Essex, U.K.",lab,both,both,NA,NA,13,13,NA,NA,NA,NA,65,65,line_mean_correlation,genetic_line,no,broad,CC,adult,adult,adult weight,relative fecundity (number of offspring produced per day),size,fertility,include,cor,0.91,"[0.70, 0.90]",95CI,NA,NA,NA,NA,NA,NA,broad_bean,table 2,size,fertility,genotype,1.527524425,13,1,1.527524425,both,adult,Insecta,between
96,Aphis fabae,285,rayyan-197247748,Variation and covariation of life history traits in aphids are related to infection with the facultative bacterial endosymbiont Hamiltonella defensa,2010,2006,Switzerland,lab,female,female,NA,NA,21,21,NA,NA,NA,NA,147,147,line_mean_correlation,genetic_line,no,broad,CC,non_adult,adult,development time,adult female body mass at maturity,reverse_maturation,size,include,cor,-0.59,0.19,se,NA,NA,NA,NA,NA,NA,all,table 3,maturation,size,genotype,-0.677666068,21,-1,0.677666068,female,cross,Insecta,between
98,Aphis fabae,94,rayyan-697471756,Phenotypic plasticity in host-plant specialisation in Aphis fabae,2005,NA,"Colchester,Essex, U.K.",lab,both,both,NA,NA,13,13,NA,NA,NA,NA,65,65,line_mean_correlation,genetic_line,no,broad,CC,non_adult,non_adult,birth weight,1/development time,size,maturation,include,cor,0.57,"[0.3, 0.86]",95CI,NA,NA,NA,NA,NA,NA,broad_bean,table 2,size,maturation,genotype,0.647522845,13,1,0.647522845,both,non_adult,Insecta,between
99,Aphis fabae,94,rayyan-697471756,Phenotypic plasticity in host-plant specialisation in Aphis fabae,2005,NA,"Colchester,Essex, U.K.",lab,both,both,NA,NA,13,13,NA,NA,NA,NA,65,65,line_mean_correlation,genetic_line,no,broad,CC,non_adult,adult,birth weight,relative fecundity (number of offspring produced per day),size,fertility,include,cor,0.63,"[0.08, 0.88]",95CI,NA,NA,NA,NA,NA,NA,broad_bean,table 2,size,fertility,genotype,0.741416144,13,1,0.741416144,both,cross,Insecta,between
103,Aphis fabae,94,rayyan-697471756,Phenotypic plasticity in host-plant specialisation in Aphis fabae,2005,NA,"Colchester,Essex, U.K.",lab,both,both,NA,NA,13,13,NA,NA,NA,NA,65,65,line_mean_correlation,genetic_line,no,broad,CC,adult,non_adult,adult weight,1/development time,size,maturation,include,cor,0.78,"[0.36, 0.93]",95CI,NA,NA,NA,NA,NA,NA,broad_bean,table 2,size,maturation,genotype,1.045370548,13,1,1.045370548,both,cross,Insecta,between
106,Aphis fabae,94,rayyan-697471756,Phenotypic plasticity in host-plant specialisation in Aphis fabae,2005,NA,"Colchester,Essex, U.K.",lab,both,both,NA,NA,13,13,NA,NA,NA,NA,65,65,line_mean_correlation,genetic_line,no,broad,CC,non_adult,non_adult,birth weight,relative growth rate,size,growth,include,cor,0.42,"[-0.19, 0.78]",95CI,NA,NA,NA,NA,NA,NA,broad_bean,table 2,size,growth,genotype,0.447692024,13,1,0.447692024,both,non_adult,Insecta,between
107,Aphis fabae,285,rayyan-197247748,Variation and covariation of life history traits in aphids are related to infection with the facultative bacterial endosymbiont Hamiltonella defensa,2010,2006,Switzerland,lab,female,female,NA,NA,21,21,NA,NA,NA,NA,147,147,line_mean_correlation,genetic_line,no,broad,CC,non_adult,non_adult,development time,newborn offspring body size,reverse_maturation,size,include,cor,-0.48,0.2,se,NA,NA,NA,NA,NA,NA,all,table 3,maturation,size,genotype,-0.522984278,21,-1,0.522984278,female,non_adult,Insecta,between
110,Aphis fabae,94,rayyan-697471756,Phenotypic plasticity in host-plant specialisation in Aphis fabae,2005,NA,"Colchester,Essex, U.K.",lab,both,both,NA,NA,13,13,NA,NA,NA,NA,65,65,line_mean_correlation,genetic_line,no,broad,CC,non_adult,adult,birth weight,adult weight,size,size,include,cor,0.86,"[0.55, 0.96]",95CI,NA,NA,NA,NA,NA,NA,nasturtium,table 2,size,size,genotype,1.293344672,13,1,1.293344672,both,cross,Insecta,within
113,Aphis fabae,94,rayyan-697471756,Phenotypic plasticity in host-plant specialisation in Aphis fabae,2005,NA,"Colchester,Essex, U.K.",lab,both,both,NA,NA,13,13,NA,NA,NA,NA,65,65,line_mean_correlation,genetic_line,no,broad,CC,non_adult,adult,birth weight,relative fecundity (number of offspring produced per day),size,fertility,include,cor,0.83,"[0.48, 0.95]",95CI,NA,NA,NA,NA,NA,NA,nasturtium,table 2,size,fertility,genotype,1.188136404,13,1,1.188136404,both,cross,Insecta,between
114,Aphis fabae,94,rayyan-697471756,Phenotypic plasticity in host-plant specialisation in Aphis fabae,2005,NA,"Colchester,Essex, U.K.",lab,both,both,NA,NA,13,13,NA,NA,NA,NA,65,65,line_mean_correlation,genetic_line,no,broad,CC,non_adult,non_adult,birth weight,relative growth rate,size,growth,include,cor,0.68,"[0.21, 0.89]",95CI,NA,NA,NA,NA,NA,NA,nasturtium,table 2,size,growth,genotype,0.829114038,13,1,0.829114038,both,non_adult,Insecta,between
117,Aphis fabae,94,rayyan-697471756,Phenotypic plasticity in host-plant specialisation in Aphis fabae,2005,NA,"Colchester,Essex, U.K.",lab,both,both,NA,NA,13,13,NA,NA,NA,NA,65,65,line_mean_correlation,genetic_line,no,broad,CC,adult,non_adult,relative fecundity (number of offspring produced per day),relative growth rate,fertility,growth,include,cor,0.58,"[0.04, 0.86]",95CI,NA,NA,NA,NA,NA,NA,nasturtium,table 2,fertility,growth,genotype,0.662462707,13,1,0.662462707,both,cross,Insecta,between
118,Aphis fabae,94,rayyan-697471756,Phenotypic plasticity in host-plant specialisation in Aphis fabae,2005,NA,"Colchester,Essex, U.K.",lab,both,both,NA,NA,13,13,NA,NA,NA,NA,65,65,line_mean_correlation,genetic_line,no,broad,CC,non_adult,non_adult,birth weight,1/development time,size,maturation,include,cor,0.68,"[0.21, 0.89]",95CI,NA,NA,NA,NA,NA,NA,nasturtium,table 2,size,maturation,genotype,0.829114038,13,1,0.829114038,both,non_adult,Insecta,between
119,Araschnia levana,252,rayyan-197247429,"Trade-offs between melanization, development time and adult size in Inachis io and Araschnia levana (Lepidoptera: Nymphalidae)?",1999,1996,Belgium,lab,male,male,14,14,NA,NA,NA,NA,NA,NA,NA,NA,animal_model,full_sib,no,narrow,authors,non_adult,adult,development time (i-iv),adult size,reverse_maturation,size,include,cor,0.448,NA,NA,NA,NA,NA,NA,NA,NA,all_short,table 3,maturation,size,family,0.482195263,14,-1,-0.482195263,male,cross,Insecta,between
120,Araschnia levana,252,rayyan-197247429,"Trade-offs between melanization, development time and adult size in Inachis io and Araschnia levana (Lepidoptera: Nymphalidae)?",1999,1996,Belgium,lab,female,female,16,16,NA,NA,NA,NA,NA,NA,NA,NA,animal_model,full_sib,no,narrow,authors,non_adult,non_adult,development time (i-iv),development time (v),reverse_maturation,reverse_maturation,include,cor,0.094,NA,NA,NA,NA,NA,NA,NA,NA,all_long,table 3,maturation,maturation,family,0.094278338,16,1,0.094278338,female,non_adult,Insecta,within
121,Araschnia levana,252,rayyan-197247429,"Trade-offs between melanization, development time and adult size in Inachis io and Araschnia levana (Lepidoptera: Nymphalidae)?",1999,1996,Belgium,lab,female,female,14,14,NA,NA,NA,NA,NA,NA,NA,NA,animal_model,full_sib,no,narrow,authors,non_adult,non_adult,development time (i-iv),development time (v),reverse_maturation,reverse_maturation,include,cor,-0.181,NA,NA,NA,NA,NA,NA,NA,NA,all_short,table 3,maturation,maturation,family,-0.183016366,14,1,-0.183016366,female,non_adult,Insecta,within
122,Araschnia levana,252,rayyan-197247429,"Trade-offs between melanization, development time and adult size in Inachis io and Araschnia levana (Lepidoptera: Nymphalidae)?",1999,1996,Belgium,lab,male,male,14,14,NA,NA,NA,NA,NA,NA,NA,NA,animal_model,full_sib,no,narrow,authors,non_adult,non_adult,development time (i-iv),development time (v),reverse_maturation,reverse_maturation,include,cor,0.241,NA,NA,NA,NA,NA,NA,NA,NA,all_short,table 3,maturation,maturation,family,0.245835504,14,1,0.245835504,male,non_adult,Insecta,within
123,Araschnia levana,252,rayyan-197247429,"Trade-offs between melanization, development time and adult size in Inachis io and Araschnia levana (Lepidoptera: Nymphalidae)?",1999,1996,Belgium,lab,male,male,16,16,NA,NA,NA,NA,NA,NA,NA,NA,animal_model,full_sib,no,narrow,authors,non_adult,adult,development time (i-iv),adult size,reverse_maturation,size,include,cor,0.23,NA,NA,NA,NA,NA,NA,NA,NA,all_long,table 3,maturation,size,family,0.234189467,16,-1,-0.234189467,male,cross,Insecta,between
124,Araschnia levana,252,rayyan-197247429,"Trade-offs between melanization, development time and adult size in Inachis io and Araschnia levana (Lepidoptera: Nymphalidae)?",1999,1996,Belgium,lab,male,male,14,14,NA,NA,NA,NA,NA,NA,NA,NA,animal_model,full_sib,no,narrow,authors,non_adult,adult,development time (v),adult size,reverse_maturation,size,include,cor,0.222,NA,NA,NA,NA,NA,NA,NA,NA,all_short,table 3,maturation,size,family,0.225758808,14,-1,-0.225758808,male,cross,Insecta,between
127,Araschnia levana,252,rayyan-197247429,"Trade-offs between melanization, development time and adult size in Inachis io and Araschnia levana (Lepidoptera: Nymphalidae)?",1999,1996,Belgium,lab,male,male,16,16,NA,NA,NA,NA,NA,NA,NA,NA,animal_model,full_sib,no,narrow,authors,non_adult,adult,development time (v),adult size,reverse_maturation,size,include,cor,-0.017,NA,NA,NA,NA,NA,NA,NA,NA,all_long,table 3,maturation,size,family,-0.017001638,16,-1,0.017001638,male,cross,Insecta,between
129,Araschnia levana,252,rayyan-197247429,"Trade-offs between melanization, development time and adult size in Inachis io and Araschnia levana (Lepidoptera: Nymphalidae)?",1999,1996,Belgium,lab,female,female,16,16,NA,NA,NA,NA,NA,NA,NA,NA,animal_model,full_sib,no,narrow,authors,non_adult,adult,development time (i-iv),adult size,reverse_maturation,size,include,cor,0.259,NA,NA,NA,NA,NA,NA,NA,NA,all_long,table 3,maturation,size,family,0.265036204,16,-1,-0.265036204,female,cross,Insecta,between
130,Araschnia levana,252,rayyan-197247429,"Trade-offs between melanization, development time and adult size in Inachis io and Araschnia levana (Lepidoptera: Nymphalidae)?",1999,1996,Belgium,lab,female,female,14,14,NA,NA,NA,NA,NA,NA,NA,NA,animal_model,full_sib,no,narrow,authors,non_adult,adult,development time (v),adult size,reverse_maturation,size,include,cor,-0.388,NA,NA,NA,NA,NA,NA,NA,NA,all_short,table 3,maturation,size,family,-0.409443429,14,-1,0.409443429,female,cross,Insecta,between
131,Araschnia levana,252,rayyan-197247429,"Trade-offs between melanization, development time and adult size in Inachis io and Araschnia levana (Lepidoptera: Nymphalidae)?",1999,1996,Belgium,lab,female,female,16,16,NA,NA,NA,NA,NA,NA,NA,NA,animal_model,full_sib,no,narrow,authors,non_adult,adult,development time (v),adult size,reverse_maturation,size,include,cor,-0.601,NA,NA,NA,NA,NA,NA,NA,NA,all_long,table 3,maturation,size,family,-0.694711148,16,-1,0.694711148,female,cross,Insecta,between
134,Araschnia levana,252,rayyan-197247429,"Trade-offs between melanization, development time and adult size in Inachis io and Araschnia levana (Lepidoptera: Nymphalidae)?",1999,1996,Belgium,lab,male,male,16,16,NA,NA,NA,NA,NA,NA,NA,NA,animal_model,full_sib,no,narrow,authors,non_adult,non_adult,development time (i-iv),development time (v),reverse_maturation,reverse_maturation,include,cor,0.074,NA,NA,NA,NA,NA,NA,NA,NA,all_long,table 3,maturation,maturation,family,0.07413552,16,1,0.07413552,male,non_adult,Insecta,within
138,Araschnia levana,252,rayyan-197247429,"Trade-offs between melanization, development time and adult size in Inachis io and Araschnia levana (Lepidoptera: Nymphalidae)?",1999,1996,Belgium,lab,female,female,14,14,NA,NA,NA,NA,NA,NA,NA,NA,animal_model,full_sib,no,narrow,authors,non_adult,adult,development time (i-iv),adult size,reverse_maturation,size,include,cor,0.377,NA,NA,NA,NA,NA,NA,NA,NA,all_short,table 3,maturation,size,family,0.39655799,14,-1,-0.39655799,female,cross,Insecta,between
142,Arctia plantaginis,324,rayyan-697472537,Evolutionary constraints of warning signals: A genetic trade-off between the efficacy of larval and adult warning coloration can maintain variation in signal expression,2016,2003,Central Finland and Åland,lab,both,female,NA,NA,NA,NA,NA,NA,NA,NA,11742,11742,animal_model,pedigree,yes,narrow,authors,non_adult,adult,pupa mass,maternal number of offspring,size,fertility,include,cor,0.4872,0.2243,se,NA,NA,NA,NA,NA,NA,rayyan-697472537,table 2,size,fertility,pedigree,0.532382265,11742,1,0.532382265,female,cross,Insecta,between
143,Arctia plantaginis,324,rayyan-697472537,Evolutionary constraints of warning signals: A genetic trade-off between the efficacy of larval and adult warning coloration can maintain variation in signal expression,2016,2003,Central Finland and Åland,lab,both,female,NA,NA,NA,NA,NA,NA,NA,NA,11742,11742,animal_model,pedigree,yes,narrow,authors,non_adult,adult,pupa mass,maternal number of eggs,size,fertility,include,cor,0.566,0.2803,se,NA,NA,NA,NA,NA,NA,rayyan-697472537,table 2,size,fertility,pedigree,0.641617671,11742,1,0.641617671,female,cross,Insecta,between
144,Arctia plantaginis,324,rayyan-697472537,Evolutionary constraints of warning signals: A genetic trade-off between the efficacy of larval and adult warning coloration can maintain variation in signal expression,2016,2003,Central Finland and Åland,lab,female,female,NA,NA,NA,NA,NA,NA,NA,NA,11742,11742,animal_model,pedigree,yes,narrow,authors,adult,adult,maternal number of eggs,maternal number of offspring,fertility,fertility,include,cor,0.6718,0.2629,se,NA,NA,NA,NA,NA,NA,rayyan-697472537,table 2,fertility,fertility,pedigree,0.814016495,11742,1,0.814016495,female,adult,Insecta,within
145,Arctia plantaginis,324,rayyan-697472537,Evolutionary constraints of warning signals: A genetic trade-off between the efficacy of larval and adult warning coloration can maintain variation in signal expression,2016,2003,Central Finland and Åland,lab,both,female,NA,NA,NA,NA,NA,NA,NA,NA,11742,11742,animal_model,pedigree,yes,narrow,authors,non_adult,adult,development time,maternal number of eggs,reverse_maturation,fertility,include,cor,0.5997,0.2906,se,NA,NA,NA,NA,NA,NA,rayyan-697472537,table 2,maturation,fertility,pedigree,0.692678562,11742,-1,-0.692678562,female,cross,Insecta,between
146,Arctia plantaginis,324,rayyan-697472537,Evolutionary constraints of warning signals: A genetic trade-off between the efficacy of larval and adult warning coloration can maintain variation in signal expression,2016,2003,Central Finland and Åland,lab,both,female,NA,NA,NA,NA,NA,NA,NA,NA,11742,11742,animal_model,pedigree,yes,narrow,authors,non_adult,adult,development time,maternal number of offspring,reverse_maturation,fertility,include,cor,0.3048,0.217,se,NA,NA,NA,NA,NA,NA,rayyan-697472537,table 2,maturation,fertility,pedigree,0.314802739,11742,-1,-0.314802739,female,cross,Insecta,between
147,Arctia plantaginis,324,rayyan-697472537,Evolutionary constraints of warning signals: A genetic trade-off between the efficacy of larval and adult warning coloration can maintain variation in signal expression,2016,2003,Central Finland and Åland,lab,both,both,NA,NA,NA,NA,NA,NA,NA,NA,11742,11742,animal_model,pedigree,yes,narrow,authors,non_adult,non_adult,pupa mass,development time,size,reverse_maturation,include,cor,-0.224,0.1377,se,NA,NA,NA,NA,NA,NA,rayyan-697472537,table 2,size,maturation,pedigree,-0.227863471,11742,-1,0.227863471,both,non_adult,Insecta,between
148,Arge,397,rayyan-697473009,Seasonally varying diet quality and the quantitative genetics of development time and body size in birch feeding insects,2001,NA,Finland,lab,male,male,NA,NA,NA,NA,20,20,NA,NA,383,38,animal_model,full_sib,no,broad,authors,non_adult,non_adult,development time,final larval mass,reverse_maturation,size,include,cor,0.713,0.122,se,NA,NA,NA,NA,NA,NA,species_5_covariance,figure 2a,maturation,size,family,0.893259641,20,-1,-0.893259641,male,non_adult,Insecta,between
150,Athalia rosae ruficornis,106,rayyan-697471796,Chemical defence in a sawfly: Genetic components of variation in relevant life-history traits,2003,NA,"Dele´mont, Switzerland",lab,male,male,13,13,NA,NA,NA,NA,NA,NA,81,81,family_mean_correlation,full_sib,no,broad,CC,non_adult,adult,mass eonymph,mass adult,size,size,include,cor,0.77,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-697471796,table 3,size,size,family,1.020327758,13,1,1.020327758,male,cross,Insecta,within
151,Athalia rosae ruficornis,106,rayyan-697471796,Chemical defence in a sawfly: Genetic components of variation in relevant life-history traits,2003,NA,"Dele´mont, Switzerland",lab,male,male,13,13,NA,NA,NA,NA,NA,NA,81,81,family_mean_correlation,full_sib,no,broad,CC,non_adult,non_adult,mass eonymph,development time egg to eonymph,size,reverse_maturation,include,cor,0.04,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-697471796,table 3,size,maturation,family,0.040021354,13,-1,-0.040021354,male,non_adult,Insecta,between
152,Athalia rosae ruficornis,106,rayyan-697471796,Chemical defence in a sawfly: Genetic components of variation in relevant life-history traits,2003,NA,"Dele´mont, Switzerland",lab,male,male,13,13,NA,NA,NA,NA,NA,NA,81,81,family_mean_correlation,full_sib,no,broad,CC,non_adult,non_adult,mass eonymph,development time eonymph to adult,size,reverse_maturation,include,cor,-0.17,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-697471796,table 3,size,maturation,family,-0.171666664,13,-1,0.171666664,male,non_adult,Insecta,between
153,Athalia rosae ruficornis,106,rayyan-697471796,Chemical defence in a sawfly: Genetic components of variation in relevant life-history traits,2003,NA,"Dele´mont, Switzerland",lab,male,male,13,13,NA,NA,NA,NA,NA,NA,81,81,family_mean_correlation,full_sib,no,broad,CC,adult,non_adult,mass adult,development time egg to eonymph,size,reverse_maturation,include,cor,-0.29,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-697471796,table 3,size,maturation,family,-0.298566264,13,-1,0.298566264,male,cross,Insecta,between
154,Athalia rosae ruficornis,106,rayyan-697471796,Chemical defence in a sawfly: Genetic components of variation in relevant life-history traits,2003,NA,"Dele´mont, Switzerland",lab,male,male,13,13,NA,NA,NA,NA,NA,NA,81,81,family_mean_correlation,full_sib,no,broad,CC,adult,non_adult,mass adult,development time eonymph to adult,size,reverse_maturation,include,cor,-0.07,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-697471796,table 3,size,maturation,family,-0.070114671,13,-1,0.070114671,male,cross,Insecta,between
155,Athalia rosae ruficornis,106,rayyan-697471796,Chemical defence in a sawfly: Genetic components of variation in relevant life-history traits,2003,NA,"Dele´mont, Switzerland",lab,male,male,13,13,NA,NA,NA,NA,NA,NA,81,81,family_mean_correlation,full_sib,no,broad,CC,non_adult,non_adult,development time egg to eonymph,development time eonymph to adult,reverse_maturation,reverse_maturation,include,cor,0.12,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-697471796,table 3,maturation,maturation,family,0.120581028,13,1,0.120581028,male,non_adult,Insecta,within
160,Bicyclus anynana,218,rayyan-197247296,Realized correlated responses to artificial selection on pre-adult life-history traits in a butterfly,2007,1988,Malawi,lab,both,both,NA,NA,7,7,NA,NA,NA,NA,559,559,correlated_selection,genetic_line,yes,broad,CC,non_adult,non_adult,egg mass,larval time,size,reverse_maturation,include,cor,0.192,NA,NA,NA,NA,NA,NA,NA,NA,pearson_both,table 3,size,maturation,genotype,0.194412895,7,-1,-0.194412895,both,non_adult,Insecta,between
163,Bicyclus anynana,218,rayyan-197247296,Realized correlated responses to artificial selection on pre-adult life-history traits in a butterfly,2007,1988,Malawi,lab,both,both,NA,NA,7,7,NA,NA,NA,NA,559,559,correlated_selection,genetic_line,yes,broad,CC,non_adult,non_adult,egg mass,pupal mass,size,size,include,cor,0.554,NA,NA,NA,NA,NA,NA,NA,NA,pearson_both,table 3,size,size,genotype,0.624134289,7,1,0.624134289,both,non_adult,Insecta,within
166,Bicyclus anynana,90,rayyan-697471742,Consequences of artificial selection on pre-adult development for adult lifespan under benign conditions in the butterfly Bicyclus anynana,2006,1988,Malawi,lab,both,both,NA,NA,7,7,NA,NA,NA,NA,700,700,line_mean_correlation,genetic_line,both,broad,CC,both,non_adult,adult lifespan,developmental time,survival,reverse_maturation,include,cor,-0.59,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-697471742,table 5,survival,maturation,genotype,-0.677666068,7,-1,0.677666068,both,cross,Insecta,between
168,Bicyclus anynana,90,rayyan-697471742,Consequences of artificial selection on pre-adult development for adult lifespan under benign conditions in the butterfly Bicyclus anynana,2006,1988,Malawi,lab,both,both,NA,NA,7,7,NA,NA,NA,NA,700,700,line_mean_correlation,genetic_line,both,broad,CC,both,non_adult,adult lifespan,egg mass,survival,size,include,cor,0.28,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-697471742,table 5,survival,size,genotype,0.287682072,7,1,0.287682072,both,cross,Insecta,between
172,Bicyclus anynana,90,rayyan-697471742,Consequences of artificial selection on pre-adult development for adult lifespan under benign conditions in the butterfly Bicyclus anynana,2006,1988,Malawi,lab,both,both,NA,NA,7,7,NA,NA,NA,NA,700,700,line_mean_correlation,genetic_line,both,broad,CC,both,non_adult,adult lifespan,pupal mass,survival,size,include,cor,-0.22,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-697471742,table 5,survival,size,genotype,-0.223656109,7,1,-0.223656109,both,cross,Insecta,between
174,Bicyclus anynana,218,rayyan-197247296,Realized correlated responses to artificial selection on pre-adult life-history traits in a butterfly,2007,1988,Malawi,lab,both,both,NA,NA,7,7,NA,NA,NA,NA,559,559,correlated_selection,genetic_line,yes,broad,CC,non_adult,non_adult,larval time,pupal mass,reverse_maturation,size,include,cor,0.455,NA,NA,NA,NA,NA,NA,NA,NA,pearson_both,table 3,maturation,size,genotype,0.490987692,7,-1,-0.490987692,both,non_adult,Insecta,between
178,Bufo calamita,119,rayyan-697471856,Reaction norms for metamorphic traits in natterjack toads to larval density and pond duration,1997,1993,Toba breeding area,field,both,both,5,5,NA,NA,NA,NA,NA,NA,100,100,family_mean_correlation,full_sib,no,broad,CC,non_adult,adult,time to metamorphosis,size at metamorphosis,reverse_maturation,size,include,cor,-0.19,NA,NA,NA,NA,NA,NA,NA,NA,low_den_long_dur,table 5,maturation,size,family,-0.192337169,5,-1,0.192337169,both,cross,Amphibia,between
179,Bufo calamita,119,rayyan-697471856,Reaction norms for metamorphic traits in natterjack toads to larval density and pond duration,1997,NA,NA,lab,both,both,5,5,NA,NA,NA,NA,NA,NA,100,100,family_mean_correlation,full_sib,no,broad,CC,non_adult,adult,time to metamorphosis,size at metamorphosis,reverse_maturation,size,include,cor,0.14,NA,NA,NA,NA,NA,NA,NA,NA,high_den_lab,table 5,maturation,size,family,0.140925576,5,-1,-0.140925576,both,cross,Amphibia,between
180,Bufo calamita,119,rayyan-697471856,Reaction norms for metamorphic traits in natterjack toads to larval density and pond duration,1997,1993,Toba breeding area,field,both,both,5,5,NA,NA,NA,NA,NA,NA,400,400,family_mean_correlation,full_sib,no,broad,CC,non_adult,adult,time to metamorphosis,size at metamorphosis,reverse_maturation,size,include,cor,0.49,NA,NA,NA,NA,NA,NA,NA,NA,high_den_short_dur,table 5,maturation,size,family,0.536060337,5,-1,-0.536060337,both,cross,Amphibia,between
181,Bufo calamita,119,rayyan-697471856,Reaction norms for metamorphic traits in natterjack toads to larval density and pond duration,1997,1993,Toba breeding area,field,both,both,5,5,NA,NA,NA,NA,NA,NA,100,100,family_mean_correlation,full_sib,no,broad,CC,non_adult,adult,time to metamorphosis,size at metamorphosis,reverse_maturation,size,include,cor,0.05,NA,NA,NA,NA,NA,NA,NA,NA,"low_den,_shot_dur",table 5,maturation,size,family,0.050041729,5,-1,-0.050041729,both,cross,Amphibia,between
182,Bufo calamita,119,rayyan-697471856,Reaction norms for metamorphic traits in natterjack toads to larval density and pond duration,1997,NA,NA,lab,both,both,5,5,NA,NA,NA,NA,NA,NA,100,100,family_mean_correlation,full_sib,no,broad,CC,non_adult,adult,time to metamorphosis,size at metamorphosis,reverse_maturation,size,include,cor,0.01,NA,NA,NA,NA,NA,NA,NA,NA,low_den_lab,table 5,maturation,size,family,0.010000333,5,-1,-0.010000333,both,cross,Amphibia,between
183,Bufo calamita,119,rayyan-697471856,Reaction norms for metamorphic traits in natterjack toads to larval density and pond duration,1997,1993,Toba breeding area,field,both,both,5,5,NA,NA,NA,NA,NA,NA,400,400,family_mean_correlation,full_sib,no,broad,CC,non_adult,adult,time to metamorphosis,size at metamorphosis,reverse_maturation,size,include,cor,0.89,NA,NA,NA,NA,NA,NA,NA,NA,high_den_long_dur,table 5,maturation,size,family,1.421925871,5,-1,-1.421925871,both,cross,Amphibia,between
184,Cabera exanthemata,63,rayyan-697471563,Latitudinal insect body size clines revisited: A critical evaluation of the saw-tooth model,2011,NA,Finland,lab,both,both,125,125,NA,NA,125,125,NA,NA,625,625,animal_model,half_sib,no,broad,authors,non_adult,non_adult,larval development time,growth rate at the larval period ,reverse_maturation,growth,include,cor,-0.912,"[-0.953, -0.850]",95CI,NA,NA,NA,NA,NA,NA,rayyan-697471563,table 2,maturation,growth,family,-1.53928414,125,-1,1.53928414,both,non_adult,Insecta,between
185,Cabera exanthemata,63,rayyan-697471563,Latitudinal insect body size clines revisited: A critical evaluation of the saw-tooth model,2011,NA,Finland,lab,both,both,125,125,NA,NA,125,125,NA,NA,625,625,animal_model,half_sib,no,broad,authors,non_adult,non_adult,pupal mass,growth rate at the larval period ,size,growth,include,cor,-0.348,"[-0.559, 0.101]",95CI,NA,NA,NA,NA,NA,NA,rayyan-697471563,table 2,size,growth,family,-0.363166365,125,1,-0.363166365,both,non_adult,Insecta,between
186,Cabera exanthemata,63,rayyan-697471563,Latitudinal insect body size clines revisited: A critical evaluation of the saw-tooth model,2011,NA,Finland,lab,both,both,125,125,NA,NA,125,125,NA,NA,625,625,animal_model,half_sib,no,broad,authors,non_adult,non_adult,pupal mass,larval development time,size,reverse_maturation,include,cor,0.53,"[0.111, 0.665]",95CI,NA,NA,NA,NA,NA,NA,rayyan-697471563,table 2,size,maturation,family,0.59014516,125,-1,-0.59014516,both,non_adult,Insecta,between
187,Cabera pusaria,63,rayyan-697471563,Latitudinal insect body size clines revisited: A critical evaluation of the saw-tooth model,2011,NA,Finland,lab,both,both,103,103,NA,NA,103,103,NA,NA,515,515,animal_model,half_sib,no,broad,authors,non_adult,non_adult,pupal mass,growth rate at the larval period ,size,growth,include,cor,0.127,"[-0.317, 0.429]",95CI,NA,NA,NA,NA,NA,NA,rayyan-697471563,table 2,size,growth,family,0.127689479,103,1,0.127689479,both,non_adult,Insecta,between
188,Cabera pusaria,63,rayyan-697471563,Latitudinal insect body size clines revisited: A critical evaluation of the saw-tooth model,2011,NA,Finland,lab,both,both,103,103,NA,NA,103,103,NA,NA,515,515,animal_model,half_sib,no,broad,authors,non_adult,non_adult,pupal mass,larval development time,size,reverse_maturation,include,cor,0.131,"[-0.336, 0.436]",95CI,NA,NA,NA,NA,NA,NA,rayyan-697471563,table 2,size,maturation,family,0.131757175,103,-1,-0.131757175,both,non_adult,Insecta,between
189,Cabera pusaria,63,rayyan-697471563,Latitudinal insect body size clines revisited: A critical evaluation of the saw-tooth model,2011,NA,Finland,lab,both,both,103,103,NA,NA,103,103,NA,NA,515,515,animal_model,half_sib,no,broad,authors,non_adult,non_adult,larval development time,growth rate at the larval period ,reverse_maturation,growth,include,cor,-0.877,"[-0.927, -0.765]",95CI,NA,NA,NA,NA,NA,NA,rayyan-697471563,table 2,maturation,growth,family,-1.362622841,103,-1,1.362622841,both,non_adult,Insecta,between
192,Caenorhabditis elegans,114,rayyan-697471838,"Quantitative trait loci affecting survival and fertility-related traits in Caenorhabditis elegans show genotype-environment interactions, pleiotropy and epistasis",1999,NA,NA,lab,both,both,NA,NA,79,80,NA,NA,NA,NA,1975,1600,line_mean_correlation,genetic_line,no,broad,authors,both,non_adult,desiccation,alpha (age of first reproduction),reverse_survival,reverse_maturation,include,cor,0.06,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-697471838,table 3,survival,maturation,genotype,0.060072156,79,1,0.060072156,both,cross,Chromadorea,between
193,Caenorhabditis elegans,114,rayyan-697471838,"Quantitative trait loci affecting survival and fertility-related traits in Caenorhabditis elegans show genotype-environment interactions, pleiotropy and epistasis",1999,NA,NA,lab,both,both,NA,NA,79,80,NA,NA,NA,NA,1975,1600,line_mean_correlation,genetic_line,no,broad,authors,both,adult,bag in liquid,total fertility 1,reverse_survival,fertility,include,cor,-0.04,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-697471838,table 3,survival,fertility,genotype,-0.040021354,79,-1,0.040021354,both,cross,Chromadorea,between
195,Caenorhabditis elegans,114,rayyan-697471838,"Quantitative trait loci affecting survival and fertility-related traits in Caenorhabditis elegans show genotype-environment interactions, pleiotropy and epistasis",1999,NA,NA,lab,both,both,NA,NA,79,80,NA,NA,NA,NA,1975,1600,line_mean_correlation,genetic_line,no,broad,authors,both,adult,bag in liquid,total fertility 2,reverse_survival,fertility,include,cor,-0.1,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-697471838,table 3,survival,fertility,genotype,-0.100335348,79,-1,0.100335348,both,cross,Chromadorea,between
199,Caenorhabditis elegans,114,rayyan-697471838,"Quantitative trait loci affecting survival and fertility-related traits in Caenorhabditis elegans show genotype-environment interactions, pleiotropy and epistasis",1999,NA,NA,lab,both,both,NA,NA,67,80,NA,NA,NA,NA,1675,1600,line_mean_correlation,genetic_line,no,broad,authors,both,adult,survival on agar,late fertility ,survival,fertility,include,cor,-0.08,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-697471838,table 3,survival,fertility,genotype,-0.080171325,67,1,-0.080171325,both,cross,Chromadorea,between
201,Caenorhabditis elegans,114,rayyan-697471838,"Quantitative trait loci affecting survival and fertility-related traits in Caenorhabditis elegans show genotype-environment interactions, pleiotropy and epistasis",1999,NA,NA,lab,both,both,NA,NA,79,79,NA,NA,NA,NA,1975,1975,line_mean_correlation,genetic_line,no,broad,authors,both,both,bag in liquid,desiccation,reverse_survival,reverse_survival,include,cor,-0.19,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-697471838,table 3,survival,survival,genotype,-0.192337169,79,1,-0.192337169,both,both,Chromadorea,within
203,Caenorhabditis elegans,242,rayyan-197247407,Properties of ethylmethane sulfonate-induced mutations affecting life-history traits in Caenorhabditis elegans and inferences about bivariate distributions of mutation effects,2000,NA,NA,lab,both,both,NA,NA,96,96,NA,NA,NA,NA,864,864,animal_model,genetic_line,no,broad,authors,adult,both,late productivity,longevity,fertility,survival,include,cor,0.47,0.21,se,NA,NA,NA,NA,NA,NA,rayyan-197247407,table 5,fertility,survival,genotype,0.510070337,96,1,0.510070337,both,cross,Chromadorea,between
204,Caenorhabditis elegans,242,rayyan-197247407,Properties of ethylmethane sulfonate-induced mutations affecting life-history traits in Caenorhabditis elegans and inferences about bivariate distributions of mutation effects,2000,NA,NA,lab,both,both,NA,NA,96,96,NA,NA,NA,NA,864,864,animal_model,genetic_line,no,broad,authors,adult,both,early productivity,longevity,fertility,survival,include,cor,0.49,0.13,se,NA,NA,NA,NA,NA,NA,rayyan-197247407,table 5,fertility,survival,genotype,0.536060337,96,1,0.536060337,both,cross,Chromadorea,between
205,Caenorhabditis elegans,242,rayyan-197247407,Properties of ethylmethane sulfonate-induced mutations affecting life-history traits in Caenorhabditis elegans and inferences about bivariate distributions of mutation effects,2000,NA,NA,lab,both,both,NA,NA,96,96,NA,NA,NA,NA,864,864,animal_model,genetic_line,no,broad,authors,adult,both,total productivity,longevity,fertility,survival,include,cor,0.58,0.16,se,NA,NA,NA,NA,NA,NA,rayyan-197247407,table 5,fertility,survival,genotype,0.662462707,96,1,0.662462707,both,cross,Chromadorea,between
207,Caenorhabditis elegans,114,rayyan-697471838,"Quantitative trait loci affecting survival and fertility-related traits in Caenorhabditis elegans show genotype-environment interactions, pleiotropy and epistasis",1999,NA,NA,lab,both,both,NA,NA,79,80,NA,NA,NA,NA,1975,1600,line_mean_correlation,genetic_line,no,broad,authors,both,adult,bag on agar,total fertility 1,reverse_survival,fertility,include,cor,0.14,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-697471838,table 3,survival,fertility,genotype,0.140925576,79,-1,-0.140925576,both,cross,Chromadorea,between
208,Caenorhabditis elegans,114,rayyan-697471838,"Quantitative trait loci affecting survival and fertility-related traits in Caenorhabditis elegans show genotype-environment interactions, pleiotropy and epistasis",1999,NA,NA,lab,both,both,NA,NA,79,80,NA,NA,NA,NA,1975,1600,line_mean_correlation,genetic_line,no,broad,authors,both,adult,bag on agar,total fertility 2,reverse_survival,fertility,include,cor,0.2,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-697471838,table 3,survival,fertility,genotype,0.202732554,79,-1,-0.202732554,both,cross,Chromadorea,between
209,Caenorhabditis elegans,114,rayyan-697471838,"Quantitative trait loci affecting survival and fertility-related traits in Caenorhabditis elegans show genotype-environment interactions, pleiotropy and epistasis",1999,NA,NA,lab,both,both,NA,NA,79,80,NA,NA,NA,NA,1975,1600,line_mean_correlation,genetic_line,no,broad,authors,both,adult,bag in liquid,early fertility ,reverse_survival,fertility,include,cor,-0.15,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-697471838,table 3,survival,fertility,genotype,-0.151140436,79,-1,0.151140436,both,cross,Chromadorea,between
212,Caenorhabditis elegans,242,rayyan-197247407,Properties of ethylmethane sulfonate-induced mutations affecting life-history traits in Caenorhabditis elegans and inferences about bivariate distributions of mutation effects,2000,NA,NA,lab,both,both,NA,NA,96,96,NA,NA,NA,NA,864,864,animal_model,genetic_line,no,broad,authors,adult,adult,total productivity,early productivity,fertility,fertility,include,cor,0.09,0.03,NA,NA,NA,NA,NA,NA,NA,rayyan-197247407,table 5,fertility,fertility,genotype,0.090244188,96,1,0.090244188,both,adult,Chromadorea,within
213,Caenorhabditis elegans,242,rayyan-197247407,Properties of ethylmethane sulfonate-induced mutations affecting life-history traits in Caenorhabditis elegans and inferences about bivariate distributions of mutation effects,2000,NA,NA,lab,both,both,NA,NA,96,96,NA,NA,NA,NA,864,864,animal_model,genetic_line,no,broad,authors,adult,adult,total productivity,late productivity,fertility,fertility,include,cor,0.74,0.072,se,NA,NA,NA,NA,NA,NA,rayyan-197247407,table 5,fertility,fertility,genotype,0.950479381,96,1,0.950479381,both,adult,Chromadorea,within
215,Caenorhabditis elegans,114,rayyan-697471838,"Quantitative trait loci affecting survival and fertility-related traits in Caenorhabditis elegans show genotype-environment interactions, pleiotropy and epistasis",1999,NA,NA,lab,both,both,NA,NA,79,80,NA,NA,NA,NA,1580,1600,line_mean_correlation,genetic_line,no,broad,authors,adult,adult,total fertility 4,early fertility ,fertility,fertility,include,cor,0.93,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-697471838,table 3,fertility,fertility,genotype,1.65839002,79,1,1.65839002,both,adult,Chromadorea,within
216,Caenorhabditis elegans,114,rayyan-697471838,"Quantitative trait loci affecting survival and fertility-related traits in Caenorhabditis elegans show genotype-environment interactions, pleiotropy and epistasis",1999,NA,NA,lab,both,both,NA,NA,79,80,NA,NA,NA,NA,1975,1600,line_mean_correlation,genetic_line,no,broad,authors,both,non_adult,bag in liquid,alpha (age of first reproduction),reverse_survival,reverse_maturation,include,cor,0.03,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-697471838,table 3,survival,maturation,genotype,0.030009005,79,1,0.030009005,both,cross,Chromadorea,between
219,Caenorhabditis elegans,114,rayyan-697471838,"Quantitative trait loci affecting survival and fertility-related traits in Caenorhabditis elegans show genotype-environment interactions, pleiotropy and epistasis",1999,NA,NA,lab,both,both,NA,NA,79,80,NA,NA,NA,NA,1975,1600,line_mean_correlation,genetic_line,no,broad,authors,adult,adult,total fertility 1,total fertility 2,fertility,fertility,include,cor,0.82,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-697471838,table 3,fertility,fertility,genotype,1.156817465,79,1,1.156817465,both,adult,Chromadorea,within
220,Caenorhabditis elegans,114,rayyan-697471838,"Quantitative trait loci affecting survival and fertility-related traits in Caenorhabditis elegans show genotype-environment interactions, pleiotropy and epistasis",1999,NA,NA,lab,both,both,NA,NA,79,80,NA,NA,NA,NA,1580,1600,line_mean_correlation,genetic_line,no,broad,authors,adult,non_adult,total fertility 2,alpha (age of first reproduction),fertility,reverse_maturation,include,cor,-0.68,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-697471838,table 3,fertility,maturation,genotype,-0.829114038,79,-1,0.829114038,both,cross,Chromadorea,between
222,Caenorhabditis elegans,114,rayyan-697471838,"Quantitative trait loci affecting survival and fertility-related traits in Caenorhabditis elegans show genotype-environment interactions, pleiotropy and epistasis",1999,NA,NA,lab,both,both,NA,NA,79,80,NA,NA,NA,NA,1975,1600,line_mean_correlation,genetic_line,no,broad,authors,both,non_adult,bag on agar,alpha (age of first reproduction),reverse_survival,reverse_maturation,include,cor,-0.19,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-697471838,table 3,survival,maturation,genotype,-0.192337169,79,1,-0.192337169,both,cross,Chromadorea,between
224,Caenorhabditis elegans,114,rayyan-697471838,"Quantitative trait loci affecting survival and fertility-related traits in Caenorhabditis elegans show genotype-environment interactions, pleiotropy and epistasis",1999,NA,NA,lab,both,both,NA,NA,79,80,NA,NA,NA,NA,1975,1600,line_mean_correlation,genetic_line,no,broad,authors,both,adult,bag on agar,early fertility ,reverse_survival,fertility,include,cor,0.15,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-697471838,table 3,survival,fertility,genotype,0.151140436,79,-1,-0.151140436,both,cross,Chromadorea,between
225,Caenorhabditis elegans,114,rayyan-697471838,"Quantitative trait loci affecting survival and fertility-related traits in Caenorhabditis elegans show genotype-environment interactions, pleiotropy and epistasis",1999,NA,NA,lab,both,both,NA,NA,79,80,NA,NA,NA,NA,1580,1600,line_mean_correlation,genetic_line,no,broad,authors,adult,adult,total fertility 5,late fertility ,fertility,fertility,include,cor,0.71,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-697471838,table 3,fertility,fertility,genotype,0.887183863,79,1,0.887183863,both,adult,Chromadorea,within
226,Caenorhabditis elegans,114,rayyan-697471838,"Quantitative trait loci affecting survival and fertility-related traits in Caenorhabditis elegans show genotype-environment interactions, pleiotropy and epistasis",1999,NA,NA,lab,both,both,NA,NA,79,80,NA,NA,NA,NA,1580,1600,line_mean_correlation,genetic_line,no,broad,authors,adult,non_adult,total fertility 2,alpha (age of first reproduction),fertility,reverse_maturation,include,cor,-0.75,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-697471838,table 3,fertility,maturation,genotype,-0.972955075,79,-1,0.972955075,both,cross,Chromadorea,between
227,Caenorhabditis elegans,114,rayyan-697471838,"Quantitative trait loci affecting survival and fertility-related traits in Caenorhabditis elegans show genotype-environment interactions, pleiotropy and epistasis",1999,NA,NA,lab,both,both,NA,NA,67,80,NA,NA,NA,NA,1675,1600,line_mean_correlation,genetic_line,no,broad,authors,both,adult,survival on agar,early fertility ,survival,fertility,include,cor,-0.12,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-697471838,table 3,survival,fertility,genotype,-0.120581028,67,1,-0.120581028,both,cross,Chromadorea,between
228,Caenorhabditis elegans,114,rayyan-697471838,"Quantitative trait loci affecting survival and fertility-related traits in Caenorhabditis elegans show genotype-environment interactions, pleiotropy and epistasis",1999,NA,NA,lab,both,both,NA,NA,79,80,NA,NA,NA,NA,1975,1600,line_mean_correlation,genetic_line,no,broad,authors,both,adult,bag on agar,late fertility ,reverse_survival,fertility,include,cor,0.22,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-697471838,table 3,survival,fertility,genotype,0.223656109,79,-1,-0.223656109,both,cross,Chromadorea,between
229,Caenorhabditis elegans,242,rayyan-197247407,Properties of ethylmethane sulfonate-induced mutations affecting life-history traits in Caenorhabditis elegans and inferences about bivariate distributions of mutation effects,2000,NA,NA,lab,both,both,NA,NA,96,96,NA,NA,NA,NA,864,864,animal_model,genetic_line,no,broad,authors,adult,adult,early productivity,late productivity,fertility,fertility,include,cor,0.38,0.16,se,NA,NA,NA,NA,NA,NA,rayyan-197247407,table 5,fertility,fertility,genotype,0.40005965,96,1,0.40005965,both,adult,Chromadorea,within
230,Caenorhabditis elegans,216,rayyan-197247293,Environmental influence on the genetic correlations between life-history traits in Caenorhabditis elegans,2007,NA,NA,lab,both,both,NA,NA,82,82,NA,NA,NA,NA,1148,1148,animal_model,genetic_line,no,broad,authors,non_adult,adult,egg size,egg number,size,fertility,include,cor,0.07,NA,NA,NA,NA,NA,NA,NA,NA,24,table 2,size,fertility,genotype,0.070114671,82,1,0.070114671,both,cross,Chromadorea,between
231,Caenorhabditis elegans,114,rayyan-697471838,"Quantitative trait loci affecting survival and fertility-related traits in Caenorhabditis elegans show genotype-environment interactions, pleiotropy and epistasis",1999,NA,NA,lab,both,both,NA,NA,79,80,NA,NA,NA,NA,1580,1600,line_mean_correlation,genetic_line,no,broad,authors,non_adult,adult,alpha (age of first reproduction),early fertility ,reverse_maturation,fertility,include,cor,-0.77,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-697471838,table 3,maturation,fertility,genotype,-1.020327758,79,-1,1.020327758,both,cross,Chromadorea,between
232,Caenorhabditis elegans,114,rayyan-697471838,"Quantitative trait loci affecting survival and fertility-related traits in Caenorhabditis elegans show genotype-environment interactions, pleiotropy and epistasis",1999,NA,NA,lab,both,both,NA,NA,79,80,NA,NA,NA,NA,1580,1600,line_mean_correlation,genetic_line,no,broad,authors,non_adult,adult,alpha (age of first reproduction),late fertility ,reverse_maturation,fertility,include,cor,-0.56,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-697471838,table 3,maturation,fertility,genotype,-0.632833187,79,-1,0.632833187,both,cross,Chromadorea,between
235,Caenorhabditis elegans,114,rayyan-697471838,"Quantitative trait loci affecting survival and fertility-related traits in Caenorhabditis elegans show genotype-environment interactions, pleiotropy and epistasis",1999,NA,NA,lab,both,both,NA,NA,79,80,NA,NA,NA,NA,1580,1600,line_mean_correlation,genetic_line,no,broad,authors,adult,adult,early fertility ,late fertility ,fertility,fertility,include,cor,0.65,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-697471838,table 3,fertility,fertility,genotype,0.775298706,79,1,0.775298706,both,adult,Chromadorea,within
237,Caenorhabditis elegans,114,rayyan-697471838,"Quantitative trait loci affecting survival and fertility-related traits in Caenorhabditis elegans show genotype-environment interactions, pleiotropy and epistasis",1999,NA,NA,lab,both,both,NA,NA,79,80,NA,NA,NA,NA,1580,1600,line_mean_correlation,genetic_line,no,broad,authors,adult,adult,total fertility 4,early fertility ,fertility,fertility,include,cor,0.78,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-697471838,table 3,fertility,fertility,genotype,1.045370548,79,1,1.045370548,both,adult,Chromadorea,within
238,Caenorhabditis elegans,114,rayyan-697471838,"Quantitative trait loci affecting survival and fertility-related traits in Caenorhabditis elegans show genotype-environment interactions, pleiotropy and epistasis",1999,NA,NA,lab,both,both,NA,NA,67,80,NA,NA,NA,NA,1675,1600,line_mean_correlation,genetic_line,no,broad,authors,both,non_adult,survival on agar,alpha (age of first reproduction),survival,reverse_maturation,include,cor,-0.08,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-697471838,table 3,survival,maturation,genotype,-0.080171325,67,-1,0.080171325,both,cross,Chromadorea,between
240,Caenorhabditis elegans,337,rayyan-697472593,Pollution breaks down the genetic architecture of life history traits in caenorhabditis elegans,2015,NA,NA,lab,both,both,NA,NA,14,14,NA,NA,NA,NA,168,168,animal_model,genetic_line,no,narrow,authors,adult,both,fertility,late growth (144 hr),fertility,growth,include,cor,-0.063,"[-0.683, 0.784]",95CI,NA,NA,NA,NA,NA,NA,uranium,table 3,fertility,growth,genotype,-0.063083548,14,1,-0.063083548,both,cross,Chromadorea,between
241,Caenorhabditis elegans,337,rayyan-697472593,Pollution breaks down the genetic architecture of life history traits in caenorhabditis elegans,2015,NA,NA,lab,both,both,NA,NA,14,14,NA,NA,NA,NA,168,168,animal_model,genetic_line,no,narrow,authors,adult,both,fertility,survival at 144h,fertility,survival,include,cor,0.371,"[-0.691, 0.863]",95CI,NA,NA,NA,NA,NA,NA,uranium,table 3,fertility,survival,genotype,0.389582211,14,1,0.389582211,both,cross,Chromadorea,between
242,Caenorhabditis elegans,114,rayyan-697471838,"Quantitative trait loci affecting survival and fertility-related traits in Caenorhabditis elegans show genotype-environment interactions, pleiotropy and epistasis",1999,NA,NA,lab,both,both,NA,NA,79,80,NA,NA,NA,NA,1975,1600,line_mean_correlation,genetic_line,no,broad,authors,both,adult,desiccation,total fertility 1,reverse_survival,fertility,include,cor,-0.06,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-697471838,table 3,survival,fertility,genotype,-0.060072156,79,-1,0.060072156,both,cross,Chromadorea,between
243,Caenorhabditis elegans,114,rayyan-697471838,"Quantitative trait loci affecting survival and fertility-related traits in Caenorhabditis elegans show genotype-environment interactions, pleiotropy and epistasis",1999,NA,NA,lab,both,both,NA,NA,79,80,NA,NA,NA,NA,1580,1600,line_mean_correlation,genetic_line,no,broad,authors,adult,adult,total fertility 5,late fertility ,fertility,fertility,include,cor,0.88,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-697471838,table 3,fertility,fertility,genotype,1.375767657,79,1,1.375767657,both,adult,Chromadorea,within
245,Caenorhabditis elegans,114,rayyan-697471838,"Quantitative trait loci affecting survival and fertility-related traits in Caenorhabditis elegans show genotype-environment interactions, pleiotropy and epistasis",1999,NA,NA,lab,both,both,NA,NA,79,80,NA,NA,NA,NA,1975,1600,line_mean_correlation,genetic_line,no,broad,authors,both,adult,desiccation,early fertility ,reverse_survival,fertility,include,cor,-0.1,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-697471838,table 3,survival,fertility,genotype,-0.100335348,79,-1,0.100335348,both,cross,Chromadorea,between
246,Caenorhabditis elegans,114,rayyan-697471838,"Quantitative trait loci affecting survival and fertility-related traits in Caenorhabditis elegans show genotype-environment interactions, pleiotropy and epistasis",1999,NA,NA,lab,both,both,NA,NA,79,80,NA,NA,NA,NA,1975,1600,line_mean_correlation,genetic_line,no,broad,authors,both,adult,bag in liquid,late fertility ,reverse_survival,fertility,include,cor,-0.02,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-697471838,table 3,survival,fertility,genotype,-0.020002667,79,-1,0.020002667,both,cross,Chromadorea,between
247,Caenorhabditis elegans,114,rayyan-697471838,"Quantitative trait loci affecting survival and fertility-related traits in Caenorhabditis elegans show genotype-environment interactions, pleiotropy and epistasis",1999,NA,NA,lab,both,both,NA,NA,79,79,NA,NA,NA,NA,1975,1975,line_mean_correlation,genetic_line,no,broad,authors,both,both,bag on agar,desiccation,reverse_survival,reverse_survival,include,cor,-0.42,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-697471838,table 3,survival,survival,genotype,-0.447692024,79,1,-0.447692024,both,both,Chromadorea,within
251,Caenorhabditis elegans,337,rayyan-697472593,Pollution breaks down the genetic architecture of life history traits in caenorhabditis elegans,2015,NA,NA,lab,both,both,NA,NA,14,14,NA,NA,NA,NA,168,168,animal_model,genetic_line,no,narrow,authors,adult,both,fertility,early growth (72 hr),fertility,growth,include,cor,-0.023,"[-0.635, 0.693]",95CI,NA,NA,NA,NA,NA,NA,uranium,table 3,fertility,growth,genotype,-0.023004057,14,1,-0.023004057,both,cross,Chromadorea,between
253,Caenorhabditis elegans,337,rayyan-697472593,Pollution breaks down the genetic architecture of life history traits in caenorhabditis elegans,2015,NA,NA,lab,both,both,NA,NA,14,14,NA,NA,NA,NA,168,168,animal_model,genetic_line,no,narrow,authors,both,both,late growth (144 hr),survival at 144h,growth,survival,include,cor,-0.839,"[-0.978, 0.588]",95CI,NA,NA,NA,NA,NA,NA,control,table 2,growth,survival,genotype,-1.21778643,14,1,-1.21778643,both,both,Chromadorea,between
254,Caenorhabditis elegans,114,rayyan-697471838,"Quantitative trait loci affecting survival and fertility-related traits in Caenorhabditis elegans show genotype-environment interactions, pleiotropy and epistasis",1999,NA,NA,lab,both,both,NA,NA,67,79,NA,NA,NA,NA,1675,1975,line_mean_correlation,genetic_line,no,broad,authors,both,both,survival in liquid,desiccation,survival,reverse_survival,include,cor,0.21,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-697471838,table 3,survival,survival,genotype,0.213171347,67,-1,-0.213171347,both,both,Chromadorea,within
256,Caenorhabditis elegans,114,rayyan-697471838,"Quantitative trait loci affecting survival and fertility-related traits in Caenorhabditis elegans show genotype-environment interactions, pleiotropy and epistasis",1999,NA,NA,lab,both,both,NA,NA,67,80,NA,NA,NA,NA,1675,1600,line_mean_correlation,genetic_line,no,broad,authors,both,adult,survival in liquid,total fertility 2,survival,fertility,include,cor,0.02,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-697471838,table 3,survival,fertility,genotype,0.020002667,67,1,0.020002667,both,cross,Chromadorea,between
257,Caenorhabditis elegans,337,rayyan-697472593,Pollution breaks down the genetic architecture of life history traits in caenorhabditis elegans,2015,NA,NA,lab,both,both,NA,NA,14,14,NA,NA,NA,NA,168,168,animal_model,genetic_line,no,narrow,authors,both,both,late growth (144 hr),survival at 144h,growth,survival,include,cor,-0.72,"[-0.948, 0.749]",95CI,NA,NA,NA,NA,NA,NA,uranium,table 3,growth,survival,genotype,-0.907644983,14,1,-0.907644983,both,both,Chromadorea,between
258,Caenorhabditis elegans,337,rayyan-697472593,Pollution breaks down the genetic architecture of life history traits in caenorhabditis elegans,2015,NA,NA,lab,both,both,NA,NA,14,14,NA,NA,NA,NA,168,168,animal_model,genetic_line,no,narrow,authors,adult,both,fertility,early growth (72 hr),fertility,growth,include,cor,0.896,"[0.514, 0.987]",95CI,NA,NA,NA,NA,NA,NA,salt,table 4,fertility,growth,genotype,1.451555392,14,1,1.451555392,both,cross,Chromadorea,between
261,Caenorhabditis elegans,216,rayyan-197247293,Environmental influence on the genetic correlations between life-history traits in Caenorhabditis elegans,2007,NA,NA,lab,both,both,NA,NA,82,82,NA,NA,NA,NA,1148,1148,animal_model,genetic_line,no,broad,authors,adult,adult,egg number,body mass at maturation,fertility,size,include,cor,0.05,NA,NA,NA,NA,NA,NA,NA,NA,12,table 2,fertility,size,genotype,0.050041729,82,1,0.050041729,both,adult,Chromadorea,between
262,Caenorhabditis elegans,337,rayyan-697472593,Pollution breaks down the genetic architecture of life history traits in caenorhabditis elegans,2015,NA,NA,lab,both,both,NA,NA,14,14,NA,NA,NA,NA,168,168,animal_model,genetic_line,no,narrow,authors,both,both,early growth (72 hr),survival at 144h,growth,survival,include,cor,0.901,"[-0.825, 0.973]",95CI,NA,NA,NA,NA,NA,NA,salt,table 4,growth,survival,genotype,1.477507746,14,1,1.477507746,both,both,Chromadorea,between
263,Caenorhabditis elegans,337,rayyan-697472593,Pollution breaks down the genetic architecture of life history traits in caenorhabditis elegans,2015,NA,NA,lab,both,both,NA,NA,14,14,NA,NA,NA,NA,168,168,animal_model,genetic_line,no,narrow,authors,both,both,late growth (144 hr),survival at 144h,growth,survival,include,cor,0.901,"[-0.722, 0.967]",95CI,NA,NA,NA,NA,NA,NA,salt,table 4,growth,survival,genotype,1.477507746,14,1,1.477507746,both,both,Chromadorea,between
264,Caenorhabditis elegans,114,rayyan-697471838,"Quantitative trait loci affecting survival and fertility-related traits in Caenorhabditis elegans show genotype-environment interactions, pleiotropy and epistasis",1999,NA,NA,lab,both,both,NA,NA,67,80,NA,NA,NA,NA,1675,1600,line_mean_correlation,genetic_line,no,broad,authors,both,adult,survival on agar,total fertility 2,survival,fertility,include,cor,-0.11,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-697471838,table 3,survival,fertility,genotype,-0.110446916,67,1,-0.110446916,both,cross,Chromadorea,between
265,Caenorhabditis elegans,114,rayyan-697471838,"Quantitative trait loci affecting survival and fertility-related traits in Caenorhabditis elegans show genotype-environment interactions, pleiotropy and epistasis",1999,NA,NA,lab,both,both,NA,NA,67,79,NA,NA,NA,NA,1675,1975,line_mean_correlation,genetic_line,no,broad,authors,both,both,survival in liquid,bag in liquid,survival,reverse_survival,include,cor,-0.65,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-697471838,table 3,survival,survival,genotype,-0.775298706,67,-1,0.775298706,both,both,Chromadorea,within
266,Caenorhabditis elegans,337,rayyan-697472593,Pollution breaks down the genetic architecture of life history traits in caenorhabditis elegans,2015,NA,NA,lab,both,both,NA,NA,14,14,NA,NA,NA,NA,168,168,animal_model,genetic_line,no,narrow,authors,both,both,early growth (72 hr),survival at 144h,growth,survival,include,cor,-0.401,"[-0.869, 0.717]",95CI,NA,NA,NA,NA,NA,NA,uranium,table 3,growth,survival,genotype,-0.424839974,14,1,-0.424839974,both,both,Chromadorea,between
267,Caenorhabditis elegans,114,rayyan-697471838,"Quantitative trait loci affecting survival and fertility-related traits in Caenorhabditis elegans show genotype-environment interactions, pleiotropy and epistasis",1999,NA,NA,lab,both,both,NA,NA,79,80,NA,NA,NA,NA,1975,1600,line_mean_correlation,genetic_line,no,broad,authors,both,adult,desiccation,total fertility 2,reverse_survival,fertility,include,cor,-0.06,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-697471838,table 3,survival,fertility,genotype,-0.060072156,79,-1,0.060072156,both,cross,Chromadorea,between
268,Caenorhabditis elegans,114,rayyan-697471838,"Quantitative trait loci affecting survival and fertility-related traits in Caenorhabditis elegans show genotype-environment interactions, pleiotropy and epistasis",1999,NA,NA,lab,both,both,NA,NA,67,80,NA,NA,NA,NA,1675,1600,line_mean_correlation,genetic_line,no,broad,authors,both,adult,survival in liquid,total fertility 1,survival,fertility,include,cor,-0.05,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-697471838,table 3,survival,fertility,genotype,-0.050041729,67,1,-0.050041729,both,cross,Chromadorea,between
269,Caenorhabditis elegans,337,rayyan-697472593,Pollution breaks down the genetic architecture of life history traits in caenorhabditis elegans,2015,NA,NA,lab,both,both,NA,NA,14,14,NA,NA,NA,NA,168,168,animal_model,genetic_line,no,narrow,authors,adult,both,fertility,survival at 144h,fertility,survival,include,cor,0.892,"[-0.804, 0.961]",95CI,NA,NA,NA,NA,NA,NA,salt,table 4,fertility,survival,genotype,1.431629261,14,1,1.431629261,both,cross,Chromadorea,between
270,Caenorhabditis elegans,337,rayyan-697472593,Pollution breaks down the genetic architecture of life history traits in caenorhabditis elegans,2015,NA,NA,lab,both,both,NA,NA,14,14,NA,NA,NA,NA,168,168,animal_model,genetic_line,no,narrow,authors,both,both,early growth (72 hr),late growth (144 hr),growth,growth,include,cor,0.811,"[0.188, 0.967]",95CI,NA,NA,NA,NA,NA,NA,salt,table 4,growth,growth,genotype,1.129943721,14,1,1.129943721,both,both,Chromadorea,within
271,Caenorhabditis elegans,337,rayyan-697472593,Pollution breaks down the genetic architecture of life history traits in caenorhabditis elegans,2015,NA,NA,lab,both,both,NA,NA,14,14,NA,NA,NA,NA,168,168,animal_model,genetic_line,no,narrow,authors,both,both,early growth (72 hr),late growth (144 hr),growth,growth,include,cor,-0.78,"[-0.967, -0.188]",95CI,NA,NA,NA,NA,NA,NA,control,table 2,growth,growth,genotype,-1.045370548,14,1,-1.045370548,both,both,Chromadorea,within
272,Caenorhabditis elegans,337,rayyan-697472593,Pollution breaks down the genetic architecture of life history traits in caenorhabditis elegans,2015,NA,NA,lab,both,both,NA,NA,14,14,NA,NA,NA,NA,168,168,animal_model,genetic_line,no,narrow,authors,adult,both,fertility,late growth (144 hr),fertility,growth,include,cor,0.774,"[0.045, 0.966]",95CI,NA,NA,NA,NA,NA,NA,salt,table 4,fertility,growth,genotype,1.030228582,14,1,1.030228582,both,cross,Chromadorea,between
274,Caenorhabditis elegans,114,rayyan-697471838,"Quantitative trait loci affecting survival and fertility-related traits in Caenorhabditis elegans show genotype-environment interactions, pleiotropy and epistasis",1999,NA,NA,lab,both,both,NA,NA,79,80,NA,NA,NA,NA,1975,1600,line_mean_correlation,genetic_line,no,broad,authors,both,adult,desiccation,late fertility ,reverse_survival,fertility,include,cor,0.02,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-697471838,table 3,survival,fertility,genotype,0.020002667,79,-1,-0.020002667,both,cross,Chromadorea,between
276,Caenorhabditis elegans,337,rayyan-697472593,Pollution breaks down the genetic architecture of life history traits in caenorhabditis elegans,2015,NA,NA,lab,both,both,NA,NA,14,14,NA,NA,NA,NA,168,168,animal_model,genetic_line,no,narrow,authors,both,both,early growth (72 hr),survival at 144h,growth,survival,include,cor,0.96,"[-0.279, 0.991]",95CI,NA,NA,NA,NA,NA,NA,control,table 2,growth,survival,genotype,1.945910149,14,1,1.945910149,both,both,Chromadorea,between
277,Caenorhabditis elegans,216,rayyan-197247293,Environmental influence on the genetic correlations between life-history traits in Caenorhabditis elegans,2007,NA,NA,lab,both,both,NA,NA,82,82,NA,NA,NA,NA,1148,1148,animal_model,genetic_line,no,broad,authors,non_adult,adult,egg size,body mass at maturation,size,size,include,cor,0.23,NA,NA,NA,NA,NA,NA,NA,NA,24,table 2,size,size,genotype,0.234189467,82,1,0.234189467,both,cross,Chromadorea,within
278,Caenorhabditis elegans,114,rayyan-697471838,"Quantitative trait loci affecting survival and fertility-related traits in Caenorhabditis elegans show genotype-environment interactions, pleiotropy and epistasis",1999,NA,NA,lab,both,both,NA,NA,67,80,NA,NA,NA,NA,1675,1600,line_mean_correlation,genetic_line,no,broad,authors,both,adult,survival on agar,total fertility 1,survival,fertility,include,cor,-0.02,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-697471838,table 3,survival,fertility,genotype,-0.020002667,67,1,-0.020002667,both,cross,Chromadorea,between
279,Caenorhabditis elegans,114,rayyan-697471838,"Quantitative trait loci affecting survival and fertility-related traits in Caenorhabditis elegans show genotype-environment interactions, pleiotropy and epistasis",1999,NA,NA,lab,both,both,NA,NA,67,80,NA,NA,NA,NA,1675,1600,line_mean_correlation,genetic_line,no,broad,authors,both,adult,survival in liquid,late fertility ,survival,fertility,include,cor,-0.04,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-697471838,table 3,survival,fertility,genotype,-0.040021354,67,1,-0.040021354,both,cross,Chromadorea,between
280,Caenorhabditis elegans,114,rayyan-697471838,"Quantitative trait loci affecting survival and fertility-related traits in Caenorhabditis elegans show genotype-environment interactions, pleiotropy and epistasis",1999,NA,NA,lab,both,both,NA,NA,67,80,NA,NA,NA,NA,1675,1600,line_mean_correlation,genetic_line,no,broad,authors,both,non_adult,survival in liquid,alpha (age of first reproduction),survival,reverse_maturation,include,cor,0.02,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-697471838,table 3,survival,maturation,genotype,0.020002667,67,-1,-0.020002667,both,cross,Chromadorea,between
281,Caenorhabditis elegans,114,rayyan-697471838,"Quantitative trait loci affecting survival and fertility-related traits in Caenorhabditis elegans show genotype-environment interactions, pleiotropy and epistasis",1999,NA,NA,lab,both,both,NA,NA,67,79,NA,NA,NA,NA,1675,1975,line_mean_correlation,genetic_line,no,broad,authors,both,both,survival on agar,desiccation,survival,reverse_survival,include,cor,-0.01,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-697471838,table 3,survival,survival,genotype,-0.010000333,67,-1,0.010000333,both,both,Chromadorea,within
282,Caenorhabditis elegans,114,rayyan-697471838,"Quantitative trait loci affecting survival and fertility-related traits in Caenorhabditis elegans show genotype-environment interactions, pleiotropy and epistasis",1999,NA,NA,lab,both,both,NA,NA,67,80,NA,NA,NA,NA,1675,1600,line_mean_correlation,genetic_line,no,broad,authors,both,adult,survival in liquid,early fertility ,survival,fertility,include,cor,0.06,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-697471838,table 3,survival,fertility,genotype,0.060072156,67,1,0.060072156,both,cross,Chromadorea,between
283,Caenorhabditis elegans,337,rayyan-697472593,Pollution breaks down the genetic architecture of life history traits in caenorhabditis elegans,2015,NA,NA,lab,both,both,NA,NA,14,14,NA,NA,NA,NA,168,168,animal_model,genetic_line,no,narrow,authors,adult,both,fertility,late growth (144 hr),fertility,growth,include,cor,-0.912,"[-0.987, -0.45]",95CI,NA,NA,NA,NA,NA,NA,control,table 2,fertility,growth,genotype,-1.53928414,14,1,-1.53928414,both,cross,Chromadorea,between
284,Caenorhabditis elegans,114,rayyan-697471838,"Quantitative trait loci affecting survival and fertility-related traits in Caenorhabditis elegans show genotype-environment interactions, pleiotropy and epistasis",1999,NA,NA,lab,both,both,NA,NA,67,79,NA,NA,NA,NA,1675,1975,line_mean_correlation,genetic_line,no,broad,authors,both,both,survival on agar,bag on agar,survival,reverse_survival,include,cor,-0.1,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-697471838,table 3,survival,survival,genotype,-0.100335348,67,-1,0.100335348,both,both,Chromadorea,within
285,Caenorhabditis elegans,337,rayyan-697472593,Pollution breaks down the genetic architecture of life history traits in caenorhabditis elegans,2015,NA,NA,lab,both,both,NA,NA,14,14,NA,NA,NA,NA,168,168,animal_model,genetic_line,no,narrow,authors,both,both,early growth (72 hr),late growth (144 hr),growth,growth,include,cor,-0.521,"[-0.835, 0.637]",95CI,NA,NA,NA,NA,NA,NA,uranium,table 3,growth,growth,genotype,-0.577711347,14,1,-0.577711347,both,both,Chromadorea,within
286,Caenorhabditis elegans,337,rayyan-697472593,Pollution breaks down the genetic architecture of life history traits in caenorhabditis elegans,2015,NA,NA,lab,both,both,NA,NA,14,14,NA,NA,NA,NA,168,168,animal_model,genetic_line,no,narrow,authors,adult,both,fertility,survival at 144h,fertility,survival,include,cor,0.924,"[-0.52, 0.985]",95CI,NA,NA,NA,NA,NA,NA,control,table 2,fertility,survival,genotype,1.615714145,14,1,1.615714145,both,cross,Chromadorea,between
287,Caenorhabditis elegans,216,rayyan-197247293,Environmental influence on the genetic correlations between life-history traits in Caenorhabditis elegans,2007,NA,NA,lab,both,both,NA,NA,82,82,NA,NA,NA,NA,1148,1148,animal_model,genetic_line,no,broad,authors,non_adult,adult,egg size,body mass at maturation,size,size,include,cor,0.15,NA,NA,NA,NA,NA,NA,NA,NA,12,table 2,size,size,genotype,0.151140436,82,1,0.151140436,both,cross,Chromadorea,within
288,Caenorhabditis elegans,216,rayyan-197247293,Environmental influence on the genetic correlations between life-history traits in Caenorhabditis elegans,2007,NA,NA,lab,both,both,NA,NA,82,82,NA,NA,NA,NA,1148,1148,animal_model,genetic_line,no,broad,authors,non_adult,adult,egg size,egg number,size,fertility,include,cor,-0.21,NA,NA,NA,NA,NA,NA,NA,NA,12,table 2,size,fertility,genotype,-0.213171347,82,1,-0.213171347,both,cross,Chromadorea,between
289,Caenorhabditis elegans,337,rayyan-697472593,Pollution breaks down the genetic architecture of life history traits in caenorhabditis elegans,2015,NA,NA,lab,both,both,NA,NA,14,14,NA,NA,NA,NA,168,168,animal_model,genetic_line,no,narrow,authors,adult,both,fertility,early growth (72 hr),fertility,growth,include,cor,0.904,"[0.361, 0.965]",95CI,NA,NA,NA,NA,NA,NA,control,table 2,fertility,growth,genotype,1.493682012,14,1,1.493682012,both,cross,Chromadorea,between
292,Caenorhabditis elegans,216,rayyan-197247293,Environmental influence on the genetic correlations between life-history traits in Caenorhabditis elegans,2007,NA,NA,lab,both,both,NA,NA,82,82,NA,NA,NA,NA,1148,1148,animal_model,genetic_line,no,broad,authors,adult,adult,egg number,body mass at maturation,fertility,size,include,cor,0.05,NA,NA,NA,NA,NA,NA,NA,NA,24,table 2,fertility,size,genotype,0.050041729,82,1,0.050041729,both,adult,Chromadorea,between
293,Callosobruchus chinensis,221,rayyan-197247308,Heritability and genetic correlation estimates for egg size and number in Callosobruchus chinensis (Coleoptera: Bruchidae),2006,NA,"Okayama, Japan",lab,female,female,NA,NA,NA,NA,NA,NA,52,52,496,496,matrix,half_sib,no,narrow,authors,non_adult,adult,egg size when young,egg number when young,size,fertility,include,cor,-0.166,0.417,se,NA,NA,NA,NA,NA,NA,rayyan-197247308,table 2,size,fertility,family,-0.167550482,52,1,-0.167550482,female,cross,Insecta,between
294,Callosobruchus chinensis,221,rayyan-197247308,Heritability and genetic correlation estimates for egg size and number in Callosobruchus chinensis (Coleoptera: Bruchidae),2006,NA,"Okayama, Japan",lab,female,female,NA,NA,NA,NA,NA,NA,52,52,496,496,matrix,half_sib,no,narrow,authors,non_adult,adult,egg size when old,egg number when old,size,fertility,include,cor,-0.107,0.598,se,NA,NA,NA,NA,NA,NA,rayyan-197247308,table 2,size,fertility,family,-0.107411176,52,1,-0.107411176,female,cross,Insecta,between
295,Callosobruchus chinensis,221,rayyan-197247308,Heritability and genetic correlation estimates for egg size and number in Callosobruchus chinensis (Coleoptera: Bruchidae),2006,NA,"Okayama, Japan",lab,female,female,NA,NA,NA,NA,NA,NA,52,52,496,496,matrix,half_sib,no,narrow,authors,non_adult,non_adult,egg size when young,egg size when old,size,size,include,cor,NA,0.315,se,NA,NA,NA,NA,NA,NA,rayyan-197247308,table 2,size,size,family,NA,52,1,NA,female,non_adult,Insecta,within
296,Callosobruchus chinensis,221,rayyan-197247308,Heritability and genetic correlation estimates for egg size and number in Callosobruchus chinensis (Coleoptera: Bruchidae),2006,NA,"Okayama, Japan",lab,female,female,NA,NA,NA,NA,NA,NA,52,52,496,496,matrix,half_sib,no,narrow,authors,non_adult,adult,egg size when old,egg number when young,size,fertility,include,cor,-0.27,0.597,se,NA,NA,NA,NA,NA,NA,rayyan-197247308,table 2,size,fertility,family,-0.276863823,52,1,-0.276863823,female,cross,Insecta,between
297,Callosobruchus chinensis,221,rayyan-197247308,Heritability and genetic correlation estimates for egg size and number in Callosobruchus chinensis (Coleoptera: Bruchidae),2006,NA,"Okayama, Japan",lab,female,female,NA,NA,NA,NA,NA,NA,52,52,496,496,matrix,half_sib,no,narrow,authors,adult,adult,egg number when young,egg number when old,fertility,fertility,include,cor,0.441,0.844,se,NA,NA,NA,NA,NA,NA,rayyan-197247308,table 2,fertility,fertility,family,0.473471561,52,1,0.473471561,female,adult,Insecta,within
298,Callosobruchus chinensis,221,rayyan-197247308,Heritability and genetic correlation estimates for egg size and number in Callosobruchus chinensis (Coleoptera: Bruchidae),2006,NA,"Okayama, Japan",lab,female,female,NA,NA,NA,NA,NA,NA,52,52,496,496,matrix,half_sib,no,narrow,authors,non_adult,adult,egg size when young,egg number when old,size,fertility,include,cor,-0.215,3.465,se,NA,NA,NA,NA,NA,NA,rayyan-197247308,table 2,size,fertility,family,-0.218407819,52,1,-0.218407819,female,cross,Insecta,between
299,Callosobruchus maculatus,234,rayyan-197247356,"Evolutionary genetics of lifespan and mortality rates in two populations of the seed beetle, Callosobruchus maculatus",2004,1989,"Ouagadougou, Burkina Faso",lab,female,female,204,204,NA,NA,204,204,51,51,1382,1382,animal_model,half_sib,no,narrow,authors,adult,both,adult body mass,adult lifespan,size,survival,include,cor,0.042,0.389,se,NA,NA,NA,NA,NA,NA,BF_female_Mung,table 3,size,survival,family,0.042024722,204,1,0.042024722,female,cross,Insecta,between
300,Callosobruchus maculatus,234,rayyan-197247356,"Evolutionary genetics of lifespan and mortality rates in two populations of the seed beetle, Callosobruchus maculatus",2004,1979,South India,lab,female,female,176,176,NA,NA,176,176,44,44,1382,1382,animal_model,half_sib,no,narrow,authors,adult,non_adult,adult body mass,development time,size,reverse_maturation,include,cor,0.107,0.436,se,NA,NA,NA,NA,NA,NA,SI_female_Cowpea,table 3,size,maturation,family,0.107411176,176,-1,-0.107411176,female,cross,Insecta,between
301,Callosobruchus maculatus,234,rayyan-197247356,"Evolutionary genetics of lifespan and mortality rates in two populations of the seed beetle, Callosobruchus maculatus",2004,1989,"Ouagadougou, Burkina Faso",lab,male,male,204,204,NA,NA,204,204,51,51,1382,1382,animal_model,half_sib,no,narrow,authors,adult,non_adult,adult body mass,development time,size,reverse_maturation,include,cor,-0.568,0.698,se,NA,NA,NA,NA,NA,NA,BF_male_Mung,table 3,size,maturation,family,-0.644565306,204,-1,0.644565306,male,cross,Insecta,between
302,Callosobruchus maculatus,234,rayyan-197247356,"Evolutionary genetics of lifespan and mortality rates in two populations of the seed beetle, Callosobruchus maculatus",2004,1979,South India,lab,male,male,176,176,NA,NA,176,176,44,44,1382,1382,animal_model,half_sib,no,narrow,authors,adult,non_adult,adult body mass,development time,size,reverse_maturation,include,cor,-0.078,0.285,se,NA,NA,NA,NA,NA,NA,SI_male_Mung,table 3,size,maturation,family,-0.078158764,176,-1,0.078158764,male,cross,Insecta,between
303,Callosobruchus maculatus,234,rayyan-197247356,"Evolutionary genetics of lifespan and mortality rates in two populations of the seed beetle, Callosobruchus maculatus",2004,1979,South India,lab,female,female,176,176,NA,NA,176,176,44,44,1382,1382,animal_model,half_sib,no,narrow,authors,adult,both,adult body mass,adult lifespan,size,survival,include,cor,0.092,0.254,se,NA,NA,NA,NA,NA,NA,SI_female_Mung,table 3,size,survival,family,0.092260889,176,1,0.092260889,female,cross,Insecta,between
304,Callosobruchus maculatus,234,rayyan-197247356,"Evolutionary genetics of lifespan and mortality rates in two populations of the seed beetle, Callosobruchus maculatus",2004,1989,"Ouagadougou, Burkina Faso",lab,female,female,204,204,NA,NA,204,204,51,51,1382,1382,animal_model,half_sib,no,narrow,authors,adult,both,adult body mass,adult lifespan,size,survival,include,cor,0.119,0.333,se,NA,NA,NA,NA,NA,NA,BF_female_Cowpea,table 3,size,survival,family,0.119566541,204,1,0.119566541,female,cross,Insecta,between
305,Callosobruchus maculatus,282,rayyan-197247707,Sex-specific genetic variances in life-history and morphological traits of the seed beetle Callosobruchus maculatus,2012,2002,"Oyo, Zaira, and Lossa in Nigeria",lab,female,female,203,165,NA,NA,203,165,47,45,1329,1265,animal_model,half_sib,no,narrow,authors,both,non_adult,longevity,developmental time,survival,reverse_maturation,include,cor,0.047,"[-0.22, 0.392]",95CI,NA,NA,NA,NA,NA,NA,female,table 4b,survival,maturation,family,0.047034654,165,-1,-0.047034654,female,cross,Insecta,between
306,Callosobruchus maculatus,234,rayyan-197247356,"Evolutionary genetics of lifespan and mortality rates in two populations of the seed beetle, Callosobruchus maculatus",2004,1979,South India,lab,male,male,176,176,NA,NA,176,176,44,44,1382,1382,animal_model,half_sib,no,narrow,authors,adult,both,adult body mass,adult lifespan,size,survival,include,cor,-0.078,0.285,se,NA,NA,NA,NA,NA,NA,SI_male_Mung,table 3,size,survival,family,-0.078158764,176,1,-0.078158764,male,cross,Insecta,between
307,Callosobruchus maculatus,234,rayyan-197247356,"Evolutionary genetics of lifespan and mortality rates in two populations of the seed beetle, Callosobruchus maculatus",2004,1989,"Ouagadougou, Burkina Faso",lab,female,female,204,204,NA,NA,204,204,51,51,1382,1382,animal_model,half_sib,no,narrow,authors,adult,non_adult,adult body mass,development time,size,reverse_maturation,include,cor,-0.264,0.404,se,NA,NA,NA,NA,NA,NA,BF_female_Cowpea,table 3,size,maturation,family,-0.270403228,204,-1,0.270403228,female,cross,Insecta,between
308,Callosobruchus maculatus,234,rayyan-197247356,"Evolutionary genetics of lifespan and mortality rates in two populations of the seed beetle, Callosobruchus maculatus",2004,1989,"Ouagadougou, Burkina Faso",lab,male,male,204,204,NA,NA,204,204,51,51,1382,1382,animal_model,half_sib,no,narrow,authors,adult,both,adult body mass,adult lifespan,size,survival,include,cor,-0.031,0.318,se,NA,NA,NA,NA,NA,NA,BF_male_Mung,table 3,size,survival,family,-0.031009936,204,1,-0.031009936,male,cross,Insecta,between
309,Callosobruchus maculatus,234,rayyan-197247356,"Evolutionary genetics of lifespan and mortality rates in two populations of the seed beetle, Callosobruchus maculatus",2004,1979,South India,lab,male,male,176,176,NA,NA,176,176,44,44,1382,1382,animal_model,half_sib,no,narrow,authors,adult,non_adult,adult body mass,development time,size,reverse_maturation,include,cor,-0.303,0.75,se,NA,NA,NA,NA,NA,NA,SI_male_Cowpea,table 3,size,maturation,family,-0.312819583,176,-1,0.312819583,male,cross,Insecta,between
310,Callosobruchus maculatus,263,rayyan-197247450,"The effect of novel environment and sex on the additive genetic variation and covariation in and between emergence body weight and development period in the cowpea weevil, Callosobruchus maculatus (Coleoptera, Bruchidae)",1997,NA,NA,lab,female,female,NA,NA,NA,NA,156,156,39,39,505,505,animal_model,full/half_sib,no,narrow,authors,adult,non_adult,emergence body weight,development time,size,reverse_maturation,include,cor,-0.394,0.217,se,NA,NA,NA,NA,NA,NA,novel_female,table 3,size,maturation,family,-0.416526303,156,-1,0.416526303,female,cross,Insecta,between
311,Callosobruchus maculatus,263,rayyan-197247450,"The effect of novel environment and sex on the additive genetic variation and covariation in and between emergence body weight and development period in the cowpea weevil, Callosobruchus maculatus (Coleoptera, Bruchidae)",1997,NA,NA,lab,female,female,NA,NA,NA,NA,156,156,39,39,531,531,animal_model,full/half_sib,no,narrow,authors,adult,non_adult,emergence body weight,development time,size,reverse_maturation,include,cor,0.554,0.455,se,NA,NA,NA,NA,NA,NA,ancestral_female,table 3,size,maturation,family,0.624134289,156,-1,-0.624134289,female,cross,Insecta,between
312,Callosobruchus maculatus,234,rayyan-197247356,"Evolutionary genetics of lifespan and mortality rates in two populations of the seed beetle, Callosobruchus maculatus",2004,1989,"Ouagadougou, Burkina Faso",lab,male,male,204,204,NA,NA,204,204,51,51,1382,1382,animal_model,half_sib,no,narrow,authors,adult,non_adult,adult body mass,development time,size,reverse_maturation,include,cor,NA,1.885,se,NA,NA,NA,NA,NA,NA,BF_male_Cowpea,table 3,size,maturation,family,NA,204,-1,NA,male,cross,Insecta,between
313,Callosobruchus maculatus,234,rayyan-197247356,"Evolutionary genetics of lifespan and mortality rates in two populations of the seed beetle, Callosobruchus maculatus",2004,1989,"Ouagadougou, Burkina Faso",lab,male,male,204,204,NA,NA,204,204,51,51,1382,1382,animal_model,half_sib,no,narrow,authors,adult,both,adult body mass,adult lifespan,size,survival,include,cor,0.41,0.256,se,NA,NA,NA,NA,NA,NA,BF_male_Cowpea,table 3,size,survival,family,0.435611223,204,1,0.435611223,male,cross,Insecta,between
314,Callosobruchus maculatus,107,rayyan-697471798,Environment-dependent reversal of a life history trade-off in the seed beetle Callosobruchus maculatus,2003,NA,"Ouagadougou, Burkina Faso",lab,female,female,432,432,NA,NA,432,432,94,94,2201,2201,animal_model,half_sib,no,narrow,authors,adult,adult,fecundity,mass at adult emergence,fertility,size,include,cor,0.57,0.13,se,NA,NA,NA,NA,NA,NA,present,table 2,fertility,size,family,0.647522845,432,1,0.647522845,female,adult,Insecta,between
315,Callosobruchus maculatus,107,rayyan-697471798,Environment-dependent reversal of a life history trade-off in the seed beetle Callosobruchus maculatus,2003,NA,"Ouagadougou, Burkina Faso",lab,female,female,432,432,NA,NA,432,432,94,94,2201,2201,animal_model,half_sib,no,narrow,authors,both,adult,longevity (female survival),mass at adult emergence,survival,size,include,cor,0.32,0.18,se,NA,NA,NA,NA,NA,NA,present,table 2,survival,size,family,0.331647109,432,1,0.331647109,female,cross,Insecta,between
316,Callosobruchus maculatus,234,rayyan-197247356,"Evolutionary genetics of lifespan and mortality rates in two populations of the seed beetle, Callosobruchus maculatus",2004,1979,South India,lab,female,female,176,176,NA,NA,176,176,44,44,1382,1382,animal_model,half_sib,no,narrow,authors,adult,both,adult body mass,adult lifespan,size,survival,include,cor,-0.252,0.393,se,NA,NA,NA,NA,NA,NA,SI_female_Cowpea,table 3,size,survival,family,-0.257547287,176,1,-0.257547287,female,cross,Insecta,between
317,Callosobruchus maculatus,234,rayyan-197247356,"Evolutionary genetics of lifespan and mortality rates in two populations of the seed beetle, Callosobruchus maculatus",2004,1979,South India,lab,female,female,176,176,NA,NA,176,176,44,44,1382,1382,animal_model,half_sib,no,narrow,authors,adult,non_adult,adult body mass,development time,size,reverse_maturation,include,cor,-0.056,0.559,se,NA,NA,NA,NA,NA,NA,SI_female_Mung,table 3,size,maturation,family,-0.056058649,176,-1,0.056058649,female,cross,Insecta,between
318,Callosobruchus maculatus,282,rayyan-197247707,Sex-specific genetic variances in life-history and morphological traits of the seed beetle Callosobruchus maculatus,2012,2002,"Oyo, Zaira, and Lossa in Nigeria",lab,male,male,203,165,NA,NA,203,165,47,45,1495,1643,animal_model,half_sib,no,narrow,authors,both,non_adult,longevity,developmental time,survival,reverse_maturation,include,cor,5.00E-04,"[-0.25, 0.357]",95CI,NA,NA,NA,NA,NA,NA,male,table 4b,survival,maturation,family,0.0005,165,-1,-0.0005,male,cross,Insecta,between
319,Callosobruchus maculatus,234,rayyan-197247356,"Evolutionary genetics of lifespan and mortality rates in two populations of the seed beetle, Callosobruchus maculatus",2004,1979,South India,lab,male,male,176,176,NA,NA,176,176,44,44,1382,1382,animal_model,half_sib,no,narrow,authors,adult,both,adult body mass,adult lifespan,size,survival,include,cor,0.159,0.496,se,NA,NA,NA,NA,NA,NA,SI_male_Cowpea,table 3,size,survival,family,0.160360592,176,1,0.160360592,male,cross,Insecta,between
320,Callosobruchus maculatus,282,rayyan-197247707,Sex-specific genetic variances in life-history and morphological traits of the seed beetle Callosobruchus maculatus,2012,2002,"Oyo, Zaira, and Lossa in Nigeria",lab,male,male,165,165,NA,NA,165,165,45,45,1643,1643,animal_model,half_sib,no,narrow,authors,adult,non_adult,weight at emergence,developmental time,size,reverse_maturation,include,cor,0.032,"[-0.277, 0.347]",95CI,NA,NA,NA,NA,NA,NA,male,table 4b,size,maturation,family,0.032010929,165,-1,-0.032010929,male,cross,Insecta,between
321,Callosobruchus maculatus,282,rayyan-197247707,Sex-specific genetic variances in life-history and morphological traits of the seed beetle Callosobruchus maculatus,2012,2002,"Oyo, Zaira, and Lossa in Nigeria",lab,female,female,165,165,NA,NA,165,165,45,45,1265,1265,animal_model,half_sib,no,narrow,authors,adult,non_adult,weight at emergence,developmental time,size,reverse_maturation,include,cor,0.005,"[-0.304, 0.295]",95CI,NA,NA,NA,NA,NA,NA,female,table 4b,size,maturation,family,0.005000042,165,-1,-0.005000042,female,cross,Insecta,between
322,Callosobruchus maculatus,107,rayyan-697471798,Environment-dependent reversal of a life history trade-off in the seed beetle Callosobruchus maculatus,2003,NA,"Ouagadougou, Burkina Faso",lab,female,female,432,432,NA,NA,432,432,94,94,2207,2207,animal_model,half_sib,no,narrow,authors,adult,both,fecundity,longevity (female survival),fertility,survival,include,cor,-0.44,0.19,se,NA,NA,NA,NA,NA,NA,absent,table 2,fertility,survival,family,-0.472230804,432,1,-0.472230804,female,cross,Insecta,between
323,Callosobruchus maculatus,107,rayyan-697471798,Environment-dependent reversal of a life history trade-off in the seed beetle Callosobruchus maculatus,2003,NA,"Ouagadougou, Burkina Faso",lab,female,female,432,432,NA,NA,432,432,94,94,2201,2201,animal_model,half_sib,no,narrow,authors,adult,both,fecundity,longevity (female survival),fertility,survival,include,cor,0.35,0.16,se,NA,NA,NA,NA,NA,NA,present,table 2,fertility,survival,family,0.365443754,432,1,0.365443754,female,cross,Insecta,between
324,Callosobruchus maculatus,282,rayyan-197247707,Sex-specific genetic variances in life-history and morphological traits of the seed beetle Callosobruchus maculatus,2012,2002,"Oyo, Zaira, and Lossa in Nigeria",lab,male,male,203,165,NA,NA,203,165,47,45,1495,165,animal_model,half_sib,no,narrow,authors,both,adult,longevity,weight at emergence,survival,size,include,cor,-0.032,"[-0.29, 0.316]",95CI,NA,NA,NA,NA,NA,NA,male,table 4b,survival,size,family,-0.032010929,165,1,-0.032010929,male,cross,Insecta,between
325,Callosobruchus maculatus,282,rayyan-197247707,Sex-specific genetic variances in life-history and morphological traits of the seed beetle Callosobruchus maculatus,2012,2002,"Oyo, Zaira, and Lossa in Nigeria",lab,female,female,203,165,NA,NA,203,165,47,45,1329,1265,animal_model,half_sib,no,narrow,authors,both,adult,longevity,weight at emergence,survival,size,include,cor,0.003,"[-0.305, 0.307]",95CI,NA,NA,NA,NA,NA,NA,female,table 4b,survival,size,family,0.003000009,165,1,0.003000009,female,cross,Insecta,between
326,Callosobruchus maculatus,263,rayyan-197247450,"The effect of novel environment and sex on the additive genetic variation and covariation in and between emergence body weight and development period in the cowpea weevil, Callosobruchus maculatus (Coleoptera, Bruchidae)",1997,NA,NA,lab,male,male,NA,NA,NA,NA,156,156,39,39,556,556,animal_model,full/half_sib,no,narrow,authors,adult,non_adult,emergence body weight,development time,size,reverse_maturation,include,cor,-0.0523,0.224,se,NA,NA,NA,NA,NA,NA,novel_male,table 3,size,maturation,family,-0.052347764,156,-1,0.052347764,male,cross,Insecta,between
327,Callosobruchus maculatus,263,rayyan-197247450,"The effect of novel environment and sex on the additive genetic variation and covariation in and between emergence body weight and development period in the cowpea weevil, Callosobruchus maculatus (Coleoptera, Bruchidae)",1997,NA,NA,lab,male,male,NA,NA,NA,NA,156,156,39,39,550,550,animal_model,full/half_sib,no,narrow,authors,adult,non_adult,emergence body weight,development time,size,reverse_maturation,include,cor,0.334,0.409,se,NA,NA,NA,NA,NA,NA,ancestral_male,table 3,size,maturation,family,0.347323778,156,-1,-0.347323778,male,cross,Insecta,between
328,Callosobruchus maculatus,107,rayyan-697471798,Environment-dependent reversal of a life history trade-off in the seed beetle Callosobruchus maculatus,2003,NA,"Ouagadougou, Burkina Faso",lab,female,female,432,432,NA,NA,432,432,94,94,2207,2207,animal_model,half_sib,no,narrow,authors,both,adult,longevity (female survival),mass at adult emergence,survival,size,include,cor,0.34,0.19,se,NA,NA,NA,NA,NA,NA,absent,table 2,survival,size,family,0.354092529,432,1,0.354092529,female,cross,Insecta,between
329,Callosobruchus maculatus,107,rayyan-697471798,Environment-dependent reversal of a life history trade-off in the seed beetle Callosobruchus maculatus,2003,NA,"Ouagadougou, Burkina Faso",lab,female,female,432,432,NA,NA,432,432,94,94,2207,2207,animal_model,half_sib,no,narrow,authors,adult,adult,fecundity,mass at adult emergence,fertility,size,include,cor,0.28,0.17,se,NA,NA,NA,NA,NA,NA,absent,table 2,fertility,size,family,0.287682072,432,1,0.287682072,female,adult,Insecta,between
330,Cervus elaphus,339,rayyan-697472613,A multivariate analysis of genetic constraints to life history evolution in a wild population of red deer,2014,1971-2007,"Inner Hebrides, Scotland",field,male,male,NA,NA,NA,NA,NA,NA,NA,NA,1114,245,animal_model,pedigree,no,narrow,authors,both,both,male survival to breeding age,male adult longevity,survival,survival,include,cor,0.625,NA,NA,NA,NA,NA,NA,NA,NA,both_sexes,table s3,survival,survival,pedigree,0.733168534,245,1,0.733168534,male,both,Mammalia,within
331,Cervus elaphus,339,rayyan-697472613,A multivariate analysis of genetic constraints to life history evolution in a wild population of red deer,2014,1971-2007,"Inner Hebrides, Scotland",field,female,female,NA,NA,NA,NA,NA,NA,NA,NA,1126,519,animal_model,pedigree,no,narrow,authors,both,non_adult,female survival to breeding age,1/female age at first reproduction,survival,maturation,include,cor,0.294,NA,NA,NA,NA,NA,NA,NA,NA,both_sexes,table s3,survival,maturation,pedigree,0.302939119,519,1,0.302939119,female,cross,Mammalia,between
332,Cervus elaphus,339,rayyan-697472613,A multivariate analysis of genetic constraints to life history evolution in a wild population of red deer,2014,1971-2007,"Inner Hebrides, Scotland",field,female,female,NA,NA,NA,NA,NA,NA,NA,NA,519,439,animal_model,pedigree,no,narrow,authors,non_adult,adult,1/female age at first reproduction,female Annual breeding success,maturation,fertility,include,cor,0.829,NA,NA,NA,NA,NA,NA,NA,NA,both_sexes,table s3,maturation,fertility,pedigree,1.184930546,439,1,1.184930546,female,cross,Mammalia,between
333,Cervus elaphus,339,rayyan-697472613,A multivariate analysis of genetic constraints to life history evolution in a wild population of red deer,2014,1971-2007,"Inner Hebrides, Scotland",field,male,male,NA,NA,NA,NA,NA,NA,NA,NA,149,245,animal_model,pedigree,no,narrow,authors,non_adult,both,1/male age at first reproduction,male adult longevity,maturation,survival,include,cor,0.19,NA,NA,NA,NA,NA,NA,NA,NA,both_sexes,table s3,maturation,survival,pedigree,0.192337169,149,1,0.192337169,male,cross,Mammalia,between
334,Cervus elaphus,339,rayyan-697472613,A multivariate analysis of genetic constraints to life history evolution in a wild population of red deer,2014,1971-2007,"Inner Hebrides, Scotland",field,female,female,NA,NA,NA,NA,NA,NA,NA,NA,519,338,animal_model,pedigree,no,narrow,authors,non_adult,both,1/female age at first reproduction,female adult longevity,maturation,survival,include,cor,-0.368,NA,NA,NA,NA,NA,NA,NA,NA,both_sexes,table s3,maturation,survival,pedigree,-0.386107852,338,1,-0.386107852,female,cross,Mammalia,between
337,Cervus elaphus,339,rayyan-697472613,A multivariate analysis of genetic constraints to life history evolution in a wild population of red deer,2014,1971-2007,"Inner Hebrides, Scotland",field,male,male,NA,NA,NA,NA,NA,NA,NA,NA,1114,149,animal_model,pedigree,no,narrow,authors,both,non_adult,male survival to breeding age,1/male age at first reproduction,survival,maturation,include,cor,0.197,NA,NA,NA,NA,NA,NA,NA,NA,both_sexes,table s3,survival,maturation,pedigree,0.199609496,149,1,0.199609496,male,cross,Mammalia,between
339,Cervus elaphus,339,rayyan-697472613,A multivariate analysis of genetic constraints to life history evolution in a wild population of red deer,2014,1971-2007,"Inner Hebrides, Scotland",field,male,male,NA,NA,NA,NA,NA,NA,NA,NA,149,570,animal_model,pedigree,no,narrow,authors,non_adult,adult,1/male age at first reproduction,male Annual breeding success,maturation,fertility,include,cor,0.765,NA,NA,NA,NA,NA,NA,NA,NA,both_sexes,table s3,maturation,fertility,pedigree,1.008160228,149,1,1.008160228,male,cross,Mammalia,between
340,Cervus elaphus,339,rayyan-697472613,A multivariate analysis of genetic constraints to life history evolution in a wild population of red deer,2014,1971-2007,"Inner Hebrides, Scotland",field,female,female,NA,NA,NA,NA,NA,NA,NA,NA,1126,338,animal_model,pedigree,no,narrow,authors,both,both,female survival to breeding age,female adult longevity,survival,survival,include,cor,0.00844,NA,NA,NA,NA,NA,NA,NA,NA,both_sexes,table s3,survival,survival,pedigree,0.0084402,338,1,0.0084402,female,both,Mammalia,within
341,Cervus elaphus,339,rayyan-697472613,A multivariate analysis of genetic constraints to life history evolution in a wild population of red deer,2014,1971-2007,"Inner Hebrides, Scotland",field,male,male,NA,NA,NA,NA,NA,NA,NA,NA,1114,570,animal_model,pedigree,no,narrow,authors,both,adult,male survival to breeding age,male Annual breeding success,survival,fertility,include,cor,0.703,NA,NA,NA,NA,NA,NA,NA,NA,both_sexes,table s3,survival,fertility,pedigree,0.873207271,570,1,0.873207271,male,cross,Mammalia,between
343,Cervus elaphus,339,rayyan-697472613,A multivariate analysis of genetic constraints to life history evolution in a wild population of red deer,2014,1971-2007,"Inner Hebrides, Scotland",field,female,female,NA,NA,NA,NA,NA,NA,NA,NA,1126,439,animal_model,pedigree,no,narrow,authors,both,adult,female survival to breeding age,female Annual breeding success,survival,fertility,include,cor,-0.221,NA,NA,NA,NA,NA,NA,NA,NA,both_sexes,table s3,survival,fertility,pedigree,-0.224707214,439,1,-0.224707214,female,cross,Mammalia,between
350,Cervus elaphus,339,rayyan-697472613,A multivariate analysis of genetic constraints to life history evolution in a wild population of red deer,2014,1971-2007,"Inner Hebrides, Scotland",field,female,female,NA,NA,NA,NA,NA,NA,NA,NA,338,439,animal_model,pedigree,no,narrow,authors,both,adult,female adult longevity,female Annual breeding success,survival,fertility,include,cor,-0.51,NA,NA,NA,NA,NA,NA,NA,NA,both_sexes,table s3,survival,fertility,pedigree,-0.562729769,338,1,-0.562729769,female,cross,Mammalia,between
353,Cervus elaphus,339,rayyan-697472613,A multivariate analysis of genetic constraints to life history evolution in a wild population of red deer,2014,1971-2007,"Inner Hebrides, Scotland",field,male,male,NA,NA,NA,NA,NA,NA,NA,NA,245,570,animal_model,pedigree,no,narrow,authors,both,adult,female adult longevity,male Annual breeding success,survival,fertility,include,cor,0.722,NA,NA,NA,NA,NA,NA,NA,NA,both_sexes,table s3,survival,fertility,pedigree,0.911810286,245,1,0.911810286,male,cross,Mammalia,between
356,Cervus elaphus,82,rayyan-697471709,Testing for genetic trade-offs between early- and late-life reproduction in a wild red deer population,2008,1971-2006,"Isle of Rum, Scotland",field,female,female,NA,NA,NA,NA,408,408,NA,NA,1667,1667,animal_model,full/half_sib,no,narrow,authors,non_adult,adult,offspring birth weight (intercept),female early life fecundity,size,fertility,include,cov,0.078378072,0.073,se,0.69,0.119,se,0.289,0.142,se,all,table 1,size,fertility,family,0.078539162,408,1,0.078539162,female,cross,Mammalia,between
360,Chiasmia clathrata,63,rayyan-697471563,Latitudinal insect body size clines revisited: A critical evaluation of the saw-tooth model,2011,NA,Finland,lab,both,both,114,114,NA,NA,114,114,NA,NA,570,570,animal_model,half_sib,no,broad,authors,non_adult,non_adult,pupal mass,larval development time,size,reverse_maturation,include,cor,-0.148,"[-0.373, 0.339]",95CI,NA,NA,NA,NA,NA,NA,rayyan-697471563,table 2,size,maturation,family,-0.149095025,114,-1,0.149095025,both,non_adult,Insecta,between
361,Chiasmia clathrata,63,rayyan-697471563,Latitudinal insect body size clines revisited: A critical evaluation of the saw-tooth model,2011,NA,Finland,lab,both,both,114,114,NA,NA,114,114,NA,NA,570,570,animal_model,half_sib,no,broad,authors,non_adult,non_adult,larval development time,growth rate at the larval period ,reverse_maturation,growth,include,cor,-0.903,"[-0.940, -0.792]",95CI,NA,NA,NA,NA,NA,NA,rayyan-697471563,table 2,maturation,growth,family,-1.488237944,114,-1,1.488237944,both,non_adult,Insecta,between
362,Chiasmia clathrata,63,rayyan-697471563,Latitudinal insect body size clines revisited: A critical evaluation of the saw-tooth model,2011,NA,Finland,lab,both,both,114,114,NA,NA,114,114,NA,NA,570,570,animal_model,half_sib,no,broad,authors,non_adult,non_adult,pupal mass,growth rate at the larval period ,size,growth,include,cor,0.211,"[-0.0305, 0.561]",95CI,NA,NA,NA,NA,NA,NA,rayyan-697471563,table 2,size,growth,family,0.214217711,114,1,0.214217711,both,non_adult,Insecta,between
375,Ciona intestinalis,342,rayyan-697472632,The genetic covariance between life cycle stages separated by metamorphosis,2014,NA,"Port Lincoln, South Australia",field,both,both,171,171,NA,NA,57,57,57,57,NA,NA,animal_model,full_sib,no,narrow,authors,non_adult,both,juvenile viability,adult viability,survival,survival,include,cor,0.1,"[-0.948, 0.999]",95CI,NA,NA,NA,NA,NA,NA,rayyan-697472632,table 1,survival,survival,family,0.100335348,171,1,0.100335348,both,cross,Ascidiacea,within
376,Ciona intestinalis,342,rayyan-697472632,The genetic covariance between life cycle stages separated by metamorphosis,2014,NA,"Port Lincoln, South Australia",field,both,both,171,171,NA,NA,57,57,57,57,NA,NA,animal_model,full_sib,no,narrow,authors,non_adult,non_adult,embryo viablility,larval viability,survival,survival,include,cor,-0.792,"[-1, -0.385]",95CI,NA,NA,NA,NA,NA,NA,rayyan-697472632,table 1,survival,survival,family,-1.076774757,171,1,-1.076774757,both,non_adult,Ascidiacea,within
377,Ciona intestinalis,342,rayyan-697472632,The genetic covariance between life cycle stages separated by metamorphosis,2014,NA,"Port Lincoln, South Australia",field,both,both,171,171,NA,NA,57,57,57,57,NA,NA,animal_model,full_sib,no,narrow,authors,non_adult,non_adult,embryo viablility,juvenile viability,survival,survival,include,cor,0.542,"[-0.312, 1]",95CI,NA,NA,NA,NA,NA,NA,rayyan-697472632,table 1,survival,survival,family,0.606983185,171,1,0.606983185,both,non_adult,Ascidiacea,within
378,Ciona intestinalis,342,rayyan-697472632,The genetic covariance between life cycle stages separated by metamorphosis,2014,NA,"Port Lincoln, South Australia",field,both,both,171,171,NA,NA,57,57,57,57,NA,NA,animal_model,full_sib,no,narrow,authors,non_adult,both,larval viability,adult viability,survival,survival,include,cor,-0.09,"[-1, 0.967]",95CI,NA,NA,NA,NA,NA,NA,rayyan-697472632,table 1,survival,survival,family,-0.090244188,171,1,-0.090244188,both,cross,Ascidiacea,within
379,Ciona intestinalis,342,rayyan-697472632,The genetic covariance between life cycle stages separated by metamorphosis,2014,NA,"Port Lincoln, South Australia",field,both,both,171,171,NA,NA,57,57,57,57,NA,NA,animal_model,full_sib,no,narrow,authors,non_adult,non_adult,larval viability,juvenile viability,survival,survival,include,cor,-0.721,"[-1, -0.09]",95CI,NA,NA,NA,NA,NA,NA,rayyan-697472632,table 1,survival,survival,family,-0.909724507,171,1,-0.909724507,both,non_adult,Ascidiacea,within
380,Ciona intestinalis,342,rayyan-697472632,The genetic covariance between life cycle stages separated by metamorphosis,2014,NA,"Port Lincoln, South Australia",field,both,both,171,171,NA,NA,57,57,57,57,NA,NA,animal_model,full_sib,no,narrow,authors,non_adult,both,embryo viablility,adult viability,survival,survival,include,cor,0.033,"[-0.965, 1]",95CI,NA,NA,NA,NA,NA,NA,rayyan-697472632,table 1,survival,survival,family,0.033011987,171,1,0.033011987,both,cross,Ascidiacea,within
381,Colias eurytheme,214,rayyan-197247288,"Parallel evolution in sympatric, hybridizing species: Performance of Colias butterflies on their introduced host plants",2007,NA,"Massachusetts, USA",lab,both,both,7,7,NA,NA,7,7,NA,NA,NA,NA,animal_model,full_sib,no,broad,authors,non_adult,non_adult,pupal weight,daily growth rate,size,growth,include,cov,NA,0.007,se,0.00024,0.00001,se,2.8,0.73,se,Vc_Colias_eurytheme,table 11,size,growth,family,NA,7,1,NA,both,non_adult,Insecta,between
382,Colias eurytheme,214,rayyan-197247288,"Parallel evolution in sympatric, hybridizing species: Performance of Colias butterflies on their introduced host plants",2007,NA,"Massachusetts, USA",lab,both,both,7,7,NA,NA,7,7,NA,NA,NA,NA,animal_model,full_sib,no,broad,authors,non_adult,non_adult,larval duration,daily growth rate,reverse_maturation,growth,include,cov,-0.992460007,0.76,se,2.47,0.79,se,2.8,0.73,se,Vc_Colias_eurytheme,table 11,maturation,growth,family,-2.788452034,7,-1,2.788452034,both,non_adult,Insecta,between
383,Colias eurytheme,214,rayyan-197247288,"Parallel evolution in sympatric, hybridizing species: Performance of Colias butterflies on their introduced host plants",2007,NA,"Massachusetts, USA",lab,both,both,7,7,NA,NA,7,7,NA,NA,NA,NA,animal_model,full_sib,no,broad,authors,non_adult,non_adult,daily growth rate,larva survivorship,growth,survival,include,cov,NA,0.027,se,2.8,0.73,se,0.0038,0.005,se,Vc_Colias_eurytheme,table 11,growth,survival,family,NA,7,1,NA,both,non_adult,Insecta,between
384,Colias eurytheme,214,rayyan-197247288,"Parallel evolution in sympatric, hybridizing species: Performance of Colias butterflies on their introduced host plants",2007,NA,"Massachusetts, USA",lab,both,both,7,7,NA,NA,7,7,NA,NA,NA,NA,animal_model,full_sib,no,broad,authors,non_adult,non_adult,pupal weight,larva survivorship,size,survival,include,cov,0.565452776,0.00035,se,0.00024,0.00001,se,0.0038,0.005,se,Vc_Colias_eurytheme,table 11,size,survival,family,0.640812875,7,1,0.640812875,both,non_adult,Insecta,between
385,Colias eurytheme,214,rayyan-197247288,"Parallel evolution in sympatric, hybridizing species: Performance of Colias butterflies on their introduced host plants",2007,NA,"Massachusetts, USA",lab,both,both,7,7,NA,NA,7,7,NA,NA,NA,NA,animal_model,full_sib,no,broad,authors,non_adult,non_adult,pupal weight,daily growth rate,size,growth,include,cov,NA,0.0046,se,0.00058,0.0003,se,NA,0.698,se,Tr_Colias_eurytheme,table 11,size,growth,family,NA,7,1,NA,both,non_adult,Insecta,between
386,Colias eurytheme,214,rayyan-197247288,"Parallel evolution in sympatric, hybridizing species: Performance of Colias butterflies on their introduced host plants",2007,NA,"Massachusetts, USA",lab,both,both,7,7,NA,NA,7,7,NA,NA,NA,NA,animal_model,full_sib,no,broad,authors,non_adult,non_adult,larval duration,larva survivorship,reverse_maturation,survival,include,cov,NA,0.024,se,2.47,0.79,se,0.0038,0.005,se,Vc_Colias_eurytheme,table 11,maturation,survival,family,NA,7,-1,NA,both,non_adult,Insecta,between
387,Colias eurytheme,214,rayyan-197247288,"Parallel evolution in sympatric, hybridizing species: Performance of Colias butterflies on their introduced host plants",2007,NA,"Massachusetts, USA",lab,both,both,7,7,NA,NA,7,7,NA,NA,NA,NA,animal_model,full_sib,no,broad,authors,non_adult,non_adult,larval duration,larva survivorship,reverse_maturation,survival,include,cov,NA,0.063,se,0.833,0.311,se,0.0217,0.0114,se,Ms_Colias_eurytheme,table 11,maturation,survival,family,NA,7,-1,NA,both,non_adult,Insecta,between
388,Colias eurytheme,214,rayyan-197247288,"Parallel evolution in sympatric, hybridizing species: Performance of Colias butterflies on their introduced host plants",2007,NA,"Massachusetts, USA",lab,both,both,7,7,NA,NA,7,7,NA,NA,NA,NA,animal_model,full_sib,no,broad,authors,non_adult,non_adult,pupal weight,larval duration,size,reverse_maturation,include,cov,NA,0.0078,se,0.00024,0.00001,se,2.47,0.79,se,Vc_Colias_eurytheme,table 11,size,maturation,family,NA,7,-1,NA,both,non_adult,Insecta,between
389,Colias eurytheme,214,rayyan-197247288,"Parallel evolution in sympatric, hybridizing species: Performance of Colias butterflies on their introduced host plants",2007,NA,"Massachusetts, USA",lab,both,both,7,7,NA,NA,7,7,NA,NA,NA,NA,animal_model,full_sib,no,broad,authors,non_adult,non_adult,larval duration,daily growth rate,reverse_maturation,growth,include,cov,NA,0.37,se,0.833,0.311,se,1.63,0.46,se,Ms_Colias_eurytheme,table 11,maturation,growth,family,NA,7,-1,NA,both,non_adult,Insecta,between
390,Colias eurytheme,214,rayyan-197247288,"Parallel evolution in sympatric, hybridizing species: Performance of Colias butterflies on their introduced host plants",2007,NA,"Massachusetts, USA",lab,both,both,7,7,NA,NA,7,7,NA,NA,NA,NA,animal_model,full_sib,no,broad,authors,non_adult,non_adult,pupal weight,daily growth rate,size,growth,include,cov,NA,0.008,se,0.00033,0.00019,se,1.63,0.46,se,Ms_Colias_eurytheme,table 11,size,growth,family,NA,7,1,NA,both,non_adult,Insecta,between
391,Colias eurytheme,214,rayyan-197247288,"Parallel evolution in sympatric, hybridizing species: Performance of Colias butterflies on their introduced host plants",2007,NA,"Massachusetts, USA",lab,both,both,7,7,NA,NA,7,7,NA,NA,NA,NA,animal_model,full_sib,no,broad,authors,non_adult,non_adult,pupal weight,larva survivorship,size,survival,include,cov,-0.343076011,0.00094,se,0.00058,0.0003,se,0.0015,0.0092,se,Tr_Colias_eurytheme,table 11,size,survival,family,-0.357574738,7,1,-0.357574738,both,non_adult,Insecta,between
392,Colias eurytheme,214,rayyan-197247288,"Parallel evolution in sympatric, hybridizing species: Performance of Colias butterflies on their introduced host plants",2007,NA,"Massachusetts, USA",lab,both,both,7,7,NA,NA,7,7,NA,NA,NA,NA,animal_model,full_sib,no,broad,authors,non_adult,non_adult,pupal weight,larva survivorship,size,survival,include,cov,NA,0.0008,se,3.00E-04,0.00017,se,0.0012,0.005,se,Cv_Colias_eurytheme,table 11,size,survival,family,NA,7,1,NA,both,non_adult,Insecta,between
393,Colias eurytheme,214,rayyan-197247288,"Parallel evolution in sympatric, hybridizing species: Performance of Colias butterflies on their introduced host plants",2007,NA,"Massachusetts, USA",lab,both,both,7,7,NA,NA,7,7,NA,NA,NA,NA,animal_model,full_sib,no,broad,authors,non_adult,non_adult,daily growth rate,larva survivorship,growth,survival,include,cov,NA,0.072,se,1.63,0.46,se,0.0217,0.0114,se,Ms_Colias_eurytheme,table 11,growth,survival,family,NA,7,1,NA,both,non_adult,Insecta,between
394,Colias eurytheme,214,rayyan-197247288,"Parallel evolution in sympatric, hybridizing species: Performance of Colias butterflies on their introduced host plants",2007,NA,"Massachusetts, USA",lab,both,both,7,7,NA,NA,7,7,NA,NA,NA,NA,animal_model,full_sib,no,broad,authors,non_adult,non_adult,larval duration,daily growth rate,reverse_maturation,growth,include,cov,NA,0.481,se,NA,0.301,se,NA,0.698,se,Tr_Colias_eurytheme,table 11,maturation,growth,family,NA,7,-1,NA,both,non_adult,Insecta,between
395,Colias eurytheme,214,rayyan-197247288,"Parallel evolution in sympatric, hybridizing species: Performance of Colias butterflies on their introduced host plants",2007,NA,"Massachusetts, USA",lab,both,both,7,7,NA,NA,7,7,NA,NA,NA,NA,animal_model,full_sib,no,broad,authors,non_adult,non_adult,pupal weight,daily growth rate,size,growth,include,cov,NA,0.009,se,3.00E-04,0.00017,se,1.24,0.56,se,Cv_Colias_eurytheme,table 11,size,growth,family,NA,7,1,NA,both,non_adult,Insecta,between
396,Colias eurytheme,214,rayyan-197247288,"Parallel evolution in sympatric, hybridizing species: Performance of Colias butterflies on their introduced host plants",2007,NA,"Massachusetts, USA",lab,both,both,7,7,NA,NA,7,7,NA,NA,NA,NA,animal_model,full_sib,no,broad,authors,non_adult,non_adult,larval duration,larva survivorship,reverse_maturation,survival,include,cov,NA,0.038,se,0.96,0.5,se,0.0012,0.005,se,Cv_Colias_eurytheme,table 11,maturation,survival,family,NA,7,-1,NA,both,non_adult,Insecta,between
397,Colias eurytheme,214,rayyan-197247288,"Parallel evolution in sympatric, hybridizing species: Performance of Colias butterflies on their introduced host plants",2007,NA,"Massachusetts, USA",lab,both,both,7,7,NA,NA,7,7,NA,NA,NA,NA,animal_model,full_sib,no,broad,authors,non_adult,non_adult,daily growth rate,larva survivorship,growth,survival,include,cov,0.744388374,0.021,se,0.369,0.256,se,0.0047,0.0043,se,Th_Colias_eurytheme,table 11,growth,survival,family,0.960250033,7,1,0.960250033,both,non_adult,Insecta,between
398,Colias eurytheme,214,rayyan-197247288,"Parallel evolution in sympatric, hybridizing species: Performance of Colias butterflies on their introduced host plants",2007,NA,"Massachusetts, USA",lab,both,both,7,7,NA,NA,7,7,NA,NA,NA,NA,animal_model,full_sib,no,broad,authors,non_adult,non_adult,pupal weight,larva survivorship,size,survival,include,cov,0.710013758,0.0006,se,0.00033,0.00019,se,0.0217,0.0114,se,Ms_Colias_eurytheme,table 11,size,survival,family,0.887211607,7,1,0.887211607,both,non_adult,Insecta,between
399,Colias eurytheme,214,rayyan-197247288,"Parallel evolution in sympatric, hybridizing species: Performance of Colias butterflies on their introduced host plants",2007,NA,"Massachusetts, USA",lab,both,both,7,7,NA,NA,7,7,NA,NA,NA,NA,animal_model,full_sib,no,broad,authors,non_adult,non_adult,pupal weight,larval duration,size,reverse_maturation,include,cov,NA,0.0056,se,0.00058,0.0003,se,NA,0.301,se,Tr_Colias_eurytheme,table 11,size,maturation,family,NA,7,-1,NA,both,non_adult,Insecta,between
400,Colias eurytheme,214,rayyan-197247288,"Parallel evolution in sympatric, hybridizing species: Performance of Colias butterflies on their introduced host plants",2007,NA,"Massachusetts, USA",lab,both,both,7,7,NA,NA,7,7,NA,NA,NA,NA,animal_model,full_sib,no,broad,authors,non_adult,non_adult,pupal weight,larval duration,size,reverse_maturation,include,cov,-0.755928946,0.0025,se,0.00014,0.00014,se,0.2,0.32,se,Th_Colias_eurytheme,table 11,size,maturation,family,-0.986646961,7,-1,0.986646961,both,non_adult,Insecta,between
401,Colias eurytheme,214,rayyan-197247288,"Parallel evolution in sympatric, hybridizing species: Performance of Colias butterflies on their introduced host plants",2007,NA,"Massachusetts, USA",lab,both,both,7,7,NA,NA,7,7,NA,NA,NA,NA,animal_model,full_sib,no,broad,authors,non_adult,non_adult,daily growth rate,larva survivorship,growth,survival,include,cov,NA,0.444,se,1.24,0.56,se,0.0012,0.005,se,Cv_Colias_eurytheme,table 11,growth,survival,family,NA,7,1,NA,both,non_adult,Insecta,between
402,Colias eurytheme,214,rayyan-197247288,"Parallel evolution in sympatric, hybridizing species: Performance of Colias butterflies on their introduced host plants",2007,NA,"Massachusetts, USA",lab,both,both,7,7,NA,NA,7,7,NA,NA,NA,NA,animal_model,full_sib,no,broad,authors,non_adult,non_adult,pupal weight,larval duration,size,reverse_maturation,include,cov,NA,0.005,se,0.00033,0.00019,se,0.833,0.311,se,Ms_Colias_eurytheme,table 11,size,maturation,family,NA,7,-1,NA,both,non_adult,Insecta,between
403,Colias eurytheme,214,rayyan-197247288,"Parallel evolution in sympatric, hybridizing species: Performance of Colias butterflies on their introduced host plants",2007,NA,"Massachusetts, USA",lab,both,both,7,7,NA,NA,7,7,NA,NA,NA,NA,animal_model,full_sib,no,broad,authors,non_adult,non_adult,daily growth rate,larva survivorship,growth,survival,include,cov,NA,0.088,se,1.81,1,se,0.0357,0.0152,se,Tp_Colias_eurytheme,table 11,growth,survival,family,NA,7,1,NA,both,non_adult,Insecta,between
404,Colias eurytheme,214,rayyan-197247288,"Parallel evolution in sympatric, hybridizing species: Performance of Colias butterflies on their introduced host plants",2007,NA,"Massachusetts, USA",lab,both,both,7,7,NA,NA,7,7,NA,NA,NA,NA,animal_model,full_sib,no,broad,authors,non_adult,non_adult,pupal weight,larval duration,size,reverse_maturation,include,cov,NA,0.008,se,3.00E-04,0.00017,se,0.96,0.5,se,Cv_Colias_eurytheme,table 11,size,maturation,family,NA,7,-1,NA,both,non_adult,Insecta,between
405,Colias eurytheme,214,rayyan-197247288,"Parallel evolution in sympatric, hybridizing species: Performance of Colias butterflies on their introduced host plants",2007,NA,"Massachusetts, USA",lab,both,both,7,7,NA,NA,7,7,NA,NA,NA,NA,animal_model,full_sib,no,broad,authors,non_adult,non_adult,larval duration,larva survivorship,reverse_maturation,survival,include,cov,NA,0.016,se,0.2,0.32,se,0.0047,0.0043,se,Th_Colias_eurytheme,table 11,maturation,survival,family,NA,7,-1,NA,both,non_adult,Insecta,between
406,Colias eurytheme,214,rayyan-197247288,"Parallel evolution in sympatric, hybridizing species: Performance of Colias butterflies on their introduced host plants",2007,NA,"Massachusetts, USA",lab,both,both,7,7,NA,NA,7,7,NA,NA,NA,NA,animal_model,full_sib,no,broad,authors,non_adult,non_adult,larval duration,daily growth rate,reverse_maturation,growth,include,cov,-0.979159531,0.28,se,0.2,0.32,se,0.369,0.256,se,Th_Colias_eurytheme,table 11,maturation,growth,family,-2.276765421,7,-1,2.276765421,both,non_adult,Insecta,between
407,Colias eurytheme,214,rayyan-197247288,"Parallel evolution in sympatric, hybridizing species: Performance of Colias butterflies on their introduced host plants",2007,NA,"Massachusetts, USA",lab,both,both,7,7,NA,NA,7,7,NA,NA,NA,NA,animal_model,full_sib,no,broad,authors,non_adult,non_adult,larval duration,daily growth rate,reverse_maturation,growth,include,cov,NA,1.63,se,7.01,3.23,se,1.81,1,se,Tp_Colias_eurytheme,table 11,maturation,growth,family,NA,7,-1,NA,both,non_adult,Insecta,between
408,Colias eurytheme,214,rayyan-197247288,"Parallel evolution in sympatric, hybridizing species: Performance of Colias butterflies on their introduced host plants",2007,NA,"Massachusetts, USA",lab,both,both,7,7,NA,NA,7,7,NA,NA,NA,NA,animal_model,full_sib,no,broad,authors,non_adult,non_adult,larval duration,larva survivorship,reverse_maturation,survival,include,cov,NA,0.045,se,NA,0.301,se,0.0015,0.0092,se,Tr_Colias_eurytheme,table 11,maturation,survival,family,NA,7,-1,NA,both,non_adult,Insecta,between
409,Colias eurytheme,214,rayyan-197247288,"Parallel evolution in sympatric, hybridizing species: Performance of Colias butterflies on their introduced host plants",2007,NA,"Massachusetts, USA",lab,both,both,7,7,NA,NA,7,7,NA,NA,NA,NA,animal_model,full_sib,no,broad,authors,non_adult,non_adult,larval duration,daily growth rate,reverse_maturation,growth,include,cov,-0.971537137,0.52,se,0.96,0.5,se,1.24,0.56,se,Cv_Colias_eurytheme,table 11,maturation,growth,family,-2.118984303,7,-1,2.118984303,both,non_adult,Insecta,between
410,Colias eurytheme,214,rayyan-197247288,"Parallel evolution in sympatric, hybridizing species: Performance of Colias butterflies on their introduced host plants",2007,NA,"Massachusetts, USA",lab,both,both,7,7,NA,NA,7,7,NA,NA,NA,NA,animal_model,full_sib,no,broad,authors,non_adult,non_adult,pupal weight,larval duration,size,reverse_maturation,include,cov,NA,0.0259,se,NA,0.00048,se,7.01,3.23,se,Tp_Colias_eurytheme,table 11,size,maturation,family,NA,7,-1,NA,both,non_adult,Insecta,between
411,Colias eurytheme,214,rayyan-197247288,"Parallel evolution in sympatric, hybridizing species: Performance of Colias butterflies on their introduced host plants",2007,NA,"Massachusetts, USA",lab,both,both,7,7,NA,NA,7,7,NA,NA,NA,NA,animal_model,full_sib,no,broad,authors,non_adult,non_adult,pupal weight,daily growth rate,size,growth,include,cov,NA,0.0227,se,NA,0.00048,se,1.81,1,se,Tp_Colias_eurytheme,table 11,size,growth,family,NA,7,1,NA,both,non_adult,Insecta,between
412,Colias eurytheme,214,rayyan-197247288,"Parallel evolution in sympatric, hybridizing species: Performance of Colias butterflies on their introduced host plants",2007,NA,"Massachusetts, USA",lab,both,both,7,7,NA,NA,7,7,NA,NA,NA,NA,animal_model,full_sib,no,broad,authors,non_adult,non_adult,larval duration,larva survivorship,reverse_maturation,survival,include,cov,-0.60169081,0.138,se,7.01,3.23,se,0.0357,0.0152,se,Tp_Colias_eurytheme,table 11,maturation,survival,family,-0.695793272,7,-1,0.695793272,both,non_adult,Insecta,between
413,Colias eurytheme,214,rayyan-197247288,"Parallel evolution in sympatric, hybridizing species: Performance of Colias butterflies on their introduced host plants",2007,NA,"Massachusetts, USA",lab,both,both,7,7,NA,NA,7,7,NA,NA,NA,NA,animal_model,full_sib,no,broad,authors,non_adult,non_adult,daily growth rate,larva survivorship,growth,survival,include,cov,NA,0.058,se,NA,0.698,se,0.0015,0.0092,se,Tr_Colias_eurytheme,table 11,growth,survival,family,NA,7,1,NA,both,non_adult,Insecta,between
414,Colias eurytheme,214,rayyan-197247288,"Parallel evolution in sympatric, hybridizing species: Performance of Colias butterflies on their introduced host plants",2007,NA,"Massachusetts, USA",lab,both,both,7,7,NA,NA,7,7,NA,NA,NA,NA,animal_model,full_sib,no,broad,authors,non_adult,non_adult,pupal weight,larva survivorship,size,survival,include,cov,NA,0.0019,se,NA,0.00048,se,0.0357,0.0152,se,Tp_Colias_eurytheme,table 11,size,survival,family,NA,7,1,NA,both,non_adult,Insecta,between
415,Colias eurytheme,214,rayyan-197247288,"Parallel evolution in sympatric, hybridizing species: Performance of Colias butterflies on their introduced host plants",2007,NA,"Massachusetts, USA",lab,both,both,7,7,NA,NA,7,7,NA,NA,NA,NA,animal_model,full_sib,no,broad,authors,non_adult,non_adult,pupal weight,larva survivorship,size,survival,include,cov,0,0.0004,se,0.00014,0.00014,se,0.0047,0.0043,se,Th_Colias_eurytheme,table 11,size,survival,family,0,7,1,0,both,non_adult,Insecta,between
416,Colias eurytheme,214,rayyan-197247288,"Parallel evolution in sympatric, hybridizing species: Performance of Colias butterflies on their introduced host plants",2007,NA,"Massachusetts, USA",lab,both,both,7,7,NA,NA,7,7,NA,NA,NA,NA,animal_model,full_sib,no,broad,authors,non_adult,non_adult,pupal weight,daily growth rate,size,growth,include,cov,0.918262258,0.0046,se,0.00014,0.00014,se,0.369,0.256,se,Th_Colias_eurytheme,table 11,size,growth,family,1.577829565,7,1,1.577829565,both,non_adult,Insecta,between
417,Colias philodice,214,rayyan-197247288,"Parallel evolution in sympatric, hybridizing species: Performance of Colias butterflies on their introduced host plants",2007,NA,"Massachusetts, USA",lab,both,both,6,6,NA,NA,6,6,NA,NA,NA,NA,animal_model,full_sib,no,broad,authors,non_adult,non_adult,pupal weight,larval duration,size,reverse_maturation,include,cov,-0.538125597,0.0197,se,0.00045,0.00021,se,4.99,2.62,se,Ms_Colias_philodice,table 11,size,maturation,family,-0.601513405,6,-1,0.601513405,both,non_adult,Insecta,between
418,Colias philodice,214,rayyan-197247288,"Parallel evolution in sympatric, hybridizing species: Performance of Colias butterflies on their introduced host plants",2007,NA,"Massachusetts, USA",lab,both,both,6,6,NA,NA,6,6,NA,NA,NA,NA,animal_model,full_sib,no,broad,authors,non_adult,non_adult,pupal weight,larva survivorship,size,survival,include,cov,0.433843555,0.0015,se,0.0011,0.0003,se,0.0213,0.0114,se,Th_Colias_philodice,table 11,size,survival,family,0.464621737,6,1,0.464621737,both,non_adult,Insecta,between
419,Colias philodice,214,rayyan-197247288,"Parallel evolution in sympatric, hybridizing species: Performance of Colias butterflies on their introduced host plants",2007,NA,"Massachusetts, USA",lab,both,both,6,6,NA,NA,6,6,NA,NA,NA,NA,animal_model,full_sib,no,broad,authors,non_adult,non_adult,pupal weight,daily growth rate,size,growth,include,cov,0.461943069,0.014,se,0.0011,0.0003,se,3.34,2.17,se,Th_Colias_philodice,table 11,size,growth,family,0.499778662,6,1,0.499778662,both,non_adult,Insecta,between
420,Colias philodice,214,rayyan-197247288,"Parallel evolution in sympatric, hybridizing species: Performance of Colias butterflies on their introduced host plants",2007,NA,"Massachusetts, USA",lab,both,both,6,6,NA,NA,6,6,NA,NA,NA,NA,animal_model,full_sib,no,broad,authors,non_adult,non_adult,larval duration,larva survivorship,reverse_maturation,survival,include,cov,NA,0.153,se,4.99,2.62,se,NA,0.0041,se,Ms_Colias_philodice,table 11,maturation,survival,family,NA,6,-1,NA,both,non_adult,Insecta,between
421,Colias philodice,214,rayyan-197247288,"Parallel evolution in sympatric, hybridizing species: Performance of Colias butterflies on their introduced host plants",2007,NA,"Massachusetts, USA",lab,both,both,6,6,NA,NA,6,6,NA,NA,NA,NA,animal_model,full_sib,no,broad,authors,non_adult,non_adult,pupal weight,daily growth rate,size,growth,include,cov,0.748667842,0.0217,se,0.00045,0.00021,se,5.34,3.81,se,Ms_Colias_philodice,table 11,size,growth,family,0.96991707,6,1,0.96991707,both,non_adult,Insecta,between
422,Colias philodice,214,rayyan-197247288,"Parallel evolution in sympatric, hybridizing species: Performance of Colias butterflies on their introduced host plants",2007,NA,"Massachusetts, USA",lab,both,both,6,6,NA,NA,6,6,NA,NA,NA,NA,animal_model,full_sib,no,broad,authors,non_adult,non_adult,larval duration,daily growth rate,reverse_maturation,growth,include,cov,NA,3.23,se,4.99,2.62,se,5.34,3.81,se,Ms_Colias_philodice,table 11,maturation,growth,family,NA,6,-1,NA,both,non_adult,Insecta,between
423,Colias philodice,214,rayyan-197247288,"Parallel evolution in sympatric, hybridizing species: Performance of Colias butterflies on their introduced host plants",2007,NA,"Massachusetts, USA",lab,both,both,6,6,NA,NA,6,6,NA,NA,NA,NA,animal_model,full_sib,no,broad,authors,non_adult,non_adult,pupal weight,daily growth rate,size,growth,include,cov,0.867210872,0.0202,se,0.00078,0.00028,se,9.01,2.5,se,Tp_Colias_philodice,table 11,size,growth,family,1.32171936,6,1,1.32171936,both,non_adult,Insecta,between
424,Colias philodice,214,rayyan-197247288,"Parallel evolution in sympatric, hybridizing species: Performance of Colias butterflies on their introduced host plants",2007,NA,"Massachusetts, USA",lab,both,both,6,6,NA,NA,6,6,NA,NA,NA,NA,animal_model,full_sib,no,broad,authors,non_adult,non_adult,pupal weight,larval duration,size,reverse_maturation,include,cov,-0.250824372,0.019,se,0.0011,0.0003,se,5.78,3.14,se,Th_Colias_philodice,table 11,size,maturation,family,-0.256292336,6,-1,0.256292336,both,non_adult,Insecta,between
425,Colias philodice,214,rayyan-197247288,"Parallel evolution in sympatric, hybridizing species: Performance of Colias butterflies on their introduced host plants",2007,NA,"Massachusetts, USA",lab,both,both,6,6,NA,NA,6,6,NA,NA,NA,NA,animal_model,full_sib,no,broad,authors,non_adult,non_adult,daily growth rate,larva survivorship,growth,survival,include,cov,NA,0.104,se,3.46,1.11,se,0.0015,0.0059,se,Vc_Colias_philodice,table 11,growth,survival,family,NA,6,1,NA,both,non_adult,Insecta,between
426,Colias philodice,214,rayyan-197247288,"Parallel evolution in sympatric, hybridizing species: Performance of Colias butterflies on their introduced host plants",2007,NA,"Massachusetts, USA",lab,both,both,6,6,NA,NA,6,6,NA,NA,NA,NA,animal_model,full_sib,no,broad,authors,non_adult,non_adult,pupal weight,larva survivorship,size,survival,include,cov,NA,0.0015,se,0.00045,0.00021,se,NA,0.0041,se,Ms_Colias_philodice,table 11,size,survival,family,NA,6,1,NA,both,non_adult,Insecta,between
427,Colias philodice,214,rayyan-197247288,"Parallel evolution in sympatric, hybridizing species: Performance of Colias butterflies on their introduced host plants",2007,NA,"Massachusetts, USA",lab,both,both,6,6,NA,NA,6,6,NA,NA,NA,NA,animal_model,full_sib,no,broad,authors,non_adult,non_adult,larval duration,larva survivorship,reverse_maturation,survival,include,cov,0.473101546,0.103,se,5.78,3.14,se,0.0213,0.0114,se,Th_Colias_philodice,table 11,maturation,survival,family,0.514058754,6,-1,-0.514058754,both,non_adult,Insecta,between
428,Colias philodice,214,rayyan-197247288,"Parallel evolution in sympatric, hybridizing species: Performance of Colias butterflies on their introduced host plants",2007,NA,"Massachusetts, USA",lab,both,both,6,6,NA,NA,6,6,NA,NA,NA,NA,animal_model,full_sib,no,broad,authors,non_adult,non_adult,daily growth rate,larva survivorship,growth,survival,include,cov,-0.23244952,0.083,se,3.34,2.17,se,0.0213,0.0114,se,Th_Colias_philodice,table 11,growth,survival,family,-0.23677735,6,1,-0.23677735,both,non_adult,Insecta,between
429,Colias philodice,214,rayyan-197247288,"Parallel evolution in sympatric, hybridizing species: Performance of Colias butterflies on their introduced host plants",2007,NA,"Massachusetts, USA",lab,both,both,6,6,NA,NA,6,6,NA,NA,NA,NA,animal_model,full_sib,no,broad,authors,non_adult,non_adult,pupal weight,larval duration,size,reverse_maturation,include,cov,0.422309476,0.02,se,4.60E-05,0.000083,se,5.15,1.72,se,Vc_Colias_philodice,table 11,size,maturation,family,0.45049946,6,-1,-0.45049946,both,non_adult,Insecta,between
430,Colias philodice,214,rayyan-197247288,"Parallel evolution in sympatric, hybridizing species: Performance of Colias butterflies on their introduced host plants",2007,NA,"Massachusetts, USA",lab,both,both,6,6,NA,NA,6,6,NA,NA,NA,NA,animal_model,full_sib,no,broad,authors,non_adult,non_adult,daily growth rate,larva survivorship,growth,survival,include,cov,-0.405465023,0.225,se,7.65,4.21,se,0.0344,0.0171,se,Tr_Colias_philodice,table 11,growth,survival,family,-0.430171978,6,1,-0.430171978,both,non_adult,Insecta,between
431,Colias philodice,214,rayyan-197247288,"Parallel evolution in sympatric, hybridizing species: Performance of Colias butterflies on their introduced host plants",2007,NA,"Massachusetts, USA",lab,both,both,6,6,NA,NA,6,6,NA,NA,NA,NA,animal_model,full_sib,no,broad,authors,non_adult,non_adult,pupal weight,larval duration,size,reverse_maturation,include,cov,-0.853110707,0.0269,se,0.00078,0.00028,se,16.37,5.47,se,Tp_Colias_philodice,table 11,size,maturation,family,-1.267470889,6,-1,1.267470889,both,non_adult,Insecta,between
432,Colias philodice,214,rayyan-197247288,"Parallel evolution in sympatric, hybridizing species: Performance of Colias butterflies on their introduced host plants",2007,NA,"Massachusetts, USA",lab,both,both,6,6,NA,NA,6,6,NA,NA,NA,NA,animal_model,full_sib,no,broad,authors,non_adult,non_adult,larval duration,daily growth rate,reverse_maturation,growth,include,cov,-0.945216364,1.28,se,5.15,1.72,se,3.46,1.11,se,Vc_Colias_philodice,table 11,maturation,growth,family,-1.784868478,6,-1,1.784868478,both,non_adult,Insecta,between
433,Colias philodice,214,rayyan-197247288,"Parallel evolution in sympatric, hybridizing species: Performance of Colias butterflies on their introduced host plants",2007,NA,"Massachusetts, USA",lab,both,both,6,6,NA,NA,6,6,NA,NA,NA,NA,animal_model,full_sib,no,broad,authors,non_adult,non_adult,pupal weight,larva survivorship,size,survival,include,cov,NA,0.0014,se,0.00078,0.00028,se,NA,0.013,se,Tp_Colias_philodice,table 11,size,survival,family,NA,6,1,NA,both,non_adult,Insecta,between
434,Colias philodice,214,rayyan-197247288,"Parallel evolution in sympatric, hybridizing species: Performance of Colias butterflies on their introduced host plants",2007,NA,"Massachusetts, USA",lab,both,both,6,6,NA,NA,6,6,NA,NA,NA,NA,animal_model,full_sib,no,broad,authors,non_adult,non_adult,pupal weight,larval duration,size,reverse_maturation,include,cov,NA,0.037,se,0.00052,0.00016,se,6.59,4.89,se,Cv_Colias_philodice,table 11,size,maturation,family,NA,6,-1,NA,both,non_adult,Insecta,between
435,Colias philodice,214,rayyan-197247288,"Parallel evolution in sympatric, hybridizing species: Performance of Colias butterflies on their introduced host plants",2007,NA,"Massachusetts, USA",lab,both,both,6,6,NA,NA,6,6,NA,NA,NA,NA,animal_model,full_sib,no,broad,authors,non_adult,non_adult,larval duration,daily growth rate,reverse_maturation,growth,include,cov,NA,2.67,se,5.78,3.14,se,3.34,2.17,se,Th_Colias_philodice,table 11,maturation,growth,family,NA,6,-1,NA,both,non_adult,Insecta,between
436,Colias philodice,214,rayyan-197247288,"Parallel evolution in sympatric, hybridizing species: Performance of Colias butterflies on their introduced host plants",2007,NA,"Massachusetts, USA",lab,both,both,6,6,NA,NA,6,6,NA,NA,NA,NA,animal_model,full_sib,no,broad,authors,non_adult,non_adult,daily growth rate,larva survivorship,growth,survival,include,cov,NA,0.175,se,9.01,2.5,se,NA,0.013,se,Tp_Colias_philodice,table 11,growth,survival,family,NA,6,1,NA,both,non_adult,Insecta,between
437,Colias philodice,214,rayyan-197247288,"Parallel evolution in sympatric, hybridizing species: Performance of Colias butterflies on their introduced host plants",2007,NA,"Massachusetts, USA",lab,both,both,6,6,NA,NA,6,6,NA,NA,NA,NA,animal_model,full_sib,no,broad,authors,non_adult,non_adult,larval duration,larva survivorship,reverse_maturation,survival,include,cov,NA,0.214,se,16.37,5.47,se,NA,0.013,se,Tp_Colias_philodice,table 11,maturation,survival,family,NA,6,-1,NA,both,non_adult,Insecta,between
438,Colias philodice,214,rayyan-197247288,"Parallel evolution in sympatric, hybridizing species: Performance of Colias butterflies on their introduced host plants",2007,NA,"Massachusetts, USA",lab,both,both,6,6,NA,NA,6,6,NA,NA,NA,NA,animal_model,full_sib,no,broad,authors,non_adult,non_adult,pupal weight,larva survivorship,size,survival,include,cov,-0.337270313,0.003,se,0.0023,0.0005,se,0.0344,0.0171,se,Tr_Colias_philodice,table 11,size,survival,family,-0.35100927,6,1,-0.35100927,both,non_adult,Insecta,between
439,Colias philodice,214,rayyan-197247288,"Parallel evolution in sympatric, hybridizing species: Performance of Colias butterflies on their introduced host plants",2007,NA,"Massachusetts, USA",lab,both,both,6,6,NA,NA,6,6,NA,NA,NA,NA,animal_model,full_sib,no,broad,authors,non_adult,non_adult,pupal weight,larval duration,size,reverse_maturation,include,cov,NA,0.032,se,0.0023,0.0005,se,1.1,1.78,se,Tr_Colias_philodice,table 11,size,maturation,family,NA,6,-1,NA,both,non_adult,Insecta,between
440,Colias philodice,214,rayyan-197247288,"Parallel evolution in sympatric, hybridizing species: Performance of Colias butterflies on their introduced host plants",2007,NA,"Massachusetts, USA",lab,both,both,6,6,NA,NA,6,6,NA,NA,NA,NA,animal_model,full_sib,no,broad,authors,non_adult,non_adult,pupal weight,daily growth rate,size,growth,include,cov,0.546930478,0.013,se,4.60E-05,0.000083,se,3.46,1.11,se,Vc_Colias_philodice,table 11,size,growth,family,0.613991163,6,1,0.613991163,both,non_adult,Insecta,between
441,Colias philodice,214,rayyan-197247288,"Parallel evolution in sympatric, hybridizing species: Performance of Colias butterflies on their introduced host plants",2007,NA,"Massachusetts, USA",lab,both,both,6,6,NA,NA,6,6,NA,NA,NA,NA,animal_model,full_sib,no,broad,authors,non_adult,non_adult,pupal weight,daily growth rate,size,growth,include,cov,NA,0.044,se,0.0023,0.0005,se,7.65,4.21,se,Tr_Colias_philodice,table 11,size,growth,family,NA,6,1,NA,both,non_adult,Insecta,between
442,Colias philodice,214,rayyan-197247288,"Parallel evolution in sympatric, hybridizing species: Performance of Colias butterflies on their introduced host plants",2007,NA,"Massachusetts, USA",lab,both,both,6,6,NA,NA,6,6,NA,NA,NA,NA,animal_model,full_sib,no,broad,authors,non_adult,non_adult,larval duration,larva survivorship,reverse_maturation,survival,include,cov,NA,0.143,se,5.15,1.72,se,0.0015,0.0059,se,Vc_Colias_philodice,table 11,maturation,survival,family,NA,6,-1,NA,both,non_adult,Insecta,between
443,Colias philodice,214,rayyan-197247288,"Parallel evolution in sympatric, hybridizing species: Performance of Colias butterflies on their introduced host plants",2007,NA,"Massachusetts, USA",lab,both,both,6,6,NA,NA,6,6,NA,NA,NA,NA,animal_model,full_sib,no,broad,authors,non_adult,non_adult,larval duration,larva survivorship,reverse_maturation,survival,include,cov,0.50893185,0.137,se,1.1,1.78,se,0.0344,0.0171,se,Tr_Colias_philodice,table 11,maturation,survival,family,0.561287189,6,-1,-0.561287189,both,non_adult,Insecta,between
444,Colias philodice,214,rayyan-197247288,"Parallel evolution in sympatric, hybridizing species: Performance of Colias butterflies on their introduced host plants",2007,NA,"Massachusetts, USA",lab,both,both,6,6,NA,NA,6,6,NA,NA,NA,NA,animal_model,full_sib,no,broad,authors,non_adult,non_adult,larval duration,daily growth rate,reverse_maturation,growth,include,cov,NA,2.8,se,1.1,1.78,se,7.65,4.21,se,Tr_Colias_philodice,table 11,maturation,growth,family,NA,6,-1,NA,both,non_adult,Insecta,between
445,Colias philodice,214,rayyan-197247288,"Parallel evolution in sympatric, hybridizing species: Performance of Colias butterflies on their introduced host plants",2007,NA,"Massachusetts, USA",lab,both,both,6,6,NA,NA,6,6,NA,NA,NA,NA,animal_model,full_sib,no,broad,authors,non_adult,non_adult,pupal weight,larva survivorship,size,survival,include,cov,-0.418762843,0.00028,se,4.60E-05,0.000083,se,0.0015,0.0059,se,Vc_Colias_philodice,table 11,size,survival,family,-0.446190836,6,1,-0.446190836,both,non_adult,Insecta,between
446,Colias philodice,214,rayyan-197247288,"Parallel evolution in sympatric, hybridizing species: Performance of Colias butterflies on their introduced host plants",2007,NA,"Massachusetts, USA",lab,both,both,6,6,NA,NA,6,6,NA,NA,NA,NA,animal_model,full_sib,no,broad,authors,non_adult,non_adult,daily growth rate,larva survivorship,growth,survival,include,cov,NA,0.113,se,5.34,2.74,se,NA,0.0066,se,Cv_Colias_philodice,table 11,growth,survival,family,NA,6,1,NA,both,non_adult,Insecta,between
447,Colias philodice,214,rayyan-197247288,"Parallel evolution in sympatric, hybridizing species: Performance of Colias butterflies on their introduced host plants",2007,NA,"Massachusetts, USA",lab,both,both,6,6,NA,NA,6,6,NA,NA,NA,NA,animal_model,full_sib,no,broad,authors,non_adult,non_adult,larval duration,daily growth rate,reverse_maturation,growth,include,cov,NA,4.02,se,6.59,4.89,se,5.34,2.74,se,Cv_Colias_philodice,table 11,maturation,growth,family,NA,6,-1,NA,both,non_adult,Insecta,between
448,Colias philodice,214,rayyan-197247288,"Parallel evolution in sympatric, hybridizing species: Performance of Colias butterflies on their introduced host plants",2007,NA,"Massachusetts, USA",lab,both,both,6,6,NA,NA,6,6,NA,NA,NA,NA,animal_model,full_sib,no,broad,authors,non_adult,non_adult,daily growth rate,larva survivorship,growth,survival,include,cov,NA,0.184,se,5.34,3.81,se,NA,0.0041,se,Ms_Colias_philodice,table 11,growth,survival,family,NA,6,1,NA,both,non_adult,Insecta,between
449,Colias philodice,214,rayyan-197247288,"Parallel evolution in sympatric, hybridizing species: Performance of Colias butterflies on their introduced host plants",2007,NA,"Massachusetts, USA",lab,both,both,6,6,NA,NA,6,6,NA,NA,NA,NA,animal_model,full_sib,no,broad,authors,non_adult,non_adult,larval duration,daily growth rate,reverse_maturation,growth,include,cov,-0.997142915,3.69,se,16.37,5.47,se,9.01,2.5,se,Tp_Colias_philodice,table 11,maturation,growth,family,-3.274835567,6,-1,3.274835567,both,non_adult,Insecta,between
450,Colias philodice,214,rayyan-197247288,"Parallel evolution in sympatric, hybridizing species: Performance of Colias butterflies on their introduced host plants",2007,NA,"Massachusetts, USA",lab,both,both,6,6,NA,NA,6,6,NA,NA,NA,NA,animal_model,full_sib,no,broad,authors,non_adult,non_adult,pupal weight,larva survivorship,size,survival,include,cov,NA,0.001,se,0.00052,0.00016,se,NA,0.0066,se,Cv_Colias_philodice,table 11,size,survival,family,NA,6,1,NA,both,non_adult,Insecta,between
451,Colias philodice,214,rayyan-197247288,"Parallel evolution in sympatric, hybridizing species: Performance of Colias butterflies on their introduced host plants",2007,NA,"Massachusetts, USA",lab,both,both,6,6,NA,NA,6,6,NA,NA,NA,NA,animal_model,full_sib,no,broad,authors,non_adult,non_adult,larval duration,larva survivorship,reverse_maturation,survival,include,cov,NA,0.211,se,6.59,4.89,se,NA,0.0066,se,Cv_Colias_philodice,table 11,maturation,survival,family,NA,6,-1,NA,both,non_adult,Insecta,between
452,Colias philodice,214,rayyan-197247288,"Parallel evolution in sympatric, hybridizing species: Performance of Colias butterflies on their introduced host plants",2007,NA,"Massachusetts, USA",lab,both,both,6,6,NA,NA,6,6,NA,NA,NA,NA,animal_model,full_sib,no,broad,authors,non_adult,non_adult,pupal weight,daily growth rate,size,growth,include,cov,NA,0.022,se,0.00052,0.00016,se,5.34,2.74,se,Cv_Colias_philodice,table 11,size,growth,family,NA,6,1,NA,both,non_adult,Insecta,between
459,Coturnix coturnix coturnix,357,rayyan-697472789,Searching for phenotypic causal networks involving complex traits: An application to European quail,2011,NA,NA,lab,female,female,NA,NA,NA,NA,NA,NA,NA,NA,849,849,animal_model,pedigree,no,narrow,authors,non_adult,non_adult,birth weight,weight at 35 days of age,size,size,include_2,cor,0.45,"[0.31, 0.58]",95CI,NA,NA,NA,NA,NA,NA,model_c,table 4,size,size,pedigree,0.484700279,849,1,0.484700279,female,non_adult,Aves,within
460,Coturnix coturnix coturnix,357,rayyan-697472789,Searching for phenotypic causal networks involving complex traits: An application to European quail,2011,NA,NA,lab,female,female,NA,NA,NA,NA,NA,NA,NA,NA,849,849,animal_model,pedigree,no,narrow,authors,non_adult,non_adult,birth weight,age at first egg,size,reverse_maturation,include_2,cor,0.21,"[0.02, 0.38]",95CI,NA,NA,NA,NA,NA,NA,model_c,table 4,size,maturation,pedigree,0.213171347,849,-1,-0.213171347,female,non_adult,Aves,between
461,Coturnix coturnix coturnix,357,rayyan-697472789,Searching for phenotypic causal networks involving complex traits: An application to European quail,2011,NA,NA,lab,female,both,NA,NA,NA,NA,NA,NA,NA,NA,849,849,animal_model,pedigree,no,narrow,authors,non_adult,non_adult,birth weight,average egg weight from 77 to 110 days of age,size,size,include_2,cor,0.8,"[0.68, 0.90]",95CI,NA,NA,NA,NA,NA,NA,model_c,table 4,size,size,pedigree,1.098612289,849,1,1.098612289,female,non_adult,Aves,within
462,Coturnix coturnix coturnix,357,rayyan-697472789,Searching for phenotypic causal networks involving complex traits: An application to European quail,2011,NA,NA,lab,female,female,NA,NA,NA,NA,NA,NA,NA,NA,849,849,animal_model,pedigree,no,narrow,authors,non_adult,adult,birth weight,numbe of eggs laid from 77 to 110 days of age,size,fertility,include_2,cor,0.07,"[-0.16, 0.29]",95CI,NA,NA,NA,NA,NA,NA,model_c,table 4,size,fertility,pedigree,0.070114671,849,1,0.070114671,female,cross,Aves,between
463,Coturnix coturnix coturnix,357,rayyan-697472789,Searching for phenotypic causal networks involving complex traits: An application to European quail,2011,NA,NA,lab,female,female,NA,NA,NA,NA,NA,NA,NA,NA,849,849,animal_model,pedigree,no,narrow,authors,non_adult,non_adult,weight at 35 days of age,age at first egg,size,reverse_maturation,include_2,cor,0.21,"[-0.14, 0.53]",95CI,NA,NA,NA,NA,NA,NA,model_c,table 4,size,maturation,pedigree,0.213171347,849,-1,-0.213171347,female,non_adult,Aves,between
464,Coturnix coturnix coturnix,357,rayyan-697472789,Searching for phenotypic causal networks involving complex traits: An application to European quail,2011,NA,NA,lab,female,both,NA,NA,NA,NA,NA,NA,NA,NA,849,849,animal_model,pedigree,no,narrow,authors,non_adult,non_adult,weight at 35 days of age,average egg weight from 77 to 110 days of age,size,size,include_2,cor,0.58,"[0.47, 0.70]",95CI,NA,NA,NA,NA,NA,NA,model_c,table 4,size,size,pedigree,0.662462707,849,1,0.662462707,female,non_adult,Aves,within
465,Coturnix coturnix coturnix,357,rayyan-697472789,Searching for phenotypic causal networks involving complex traits: An application to European quail,2011,NA,NA,lab,female,female,NA,NA,NA,NA,NA,NA,NA,NA,849,849,animal_model,pedigree,no,narrow,authors,non_adult,adult,weight at 35 days of age,numbe of eggs laid from 77 to 110 days of age,size,fertility,include_2,cor,0.19,"[-0.05, 0.43]",95CI,NA,NA,NA,NA,NA,NA,model_c,table 4,size,fertility,pedigree,0.192337169,849,1,0.192337169,female,cross,Aves,between
479,Coturnix coturnix coturnix,357,rayyan-697472789,Searching for phenotypic causal networks involving complex traits: An application to European quail,2011,NA,NA,lab,female,both,NA,NA,NA,NA,NA,NA,NA,NA,849,849,animal_model,pedigree,no,narrow,authors,non_adult,non_adult,age at first egg,average egg weight from 77 to 110 days of age,reverse_maturation,size,include_2,cor,0.16,"[-0.05, 0.38]",95CI,NA,NA,NA,NA,NA,NA,model_c,table 4,maturation,size,pedigree,0.161386696,849,-1,-0.161386696,female,non_adult,Aves,between
480,Coturnix coturnix coturnix,357,rayyan-697472789,Searching for phenotypic causal networks involving complex traits: An application to European quail,2011,NA,NA,lab,female,female,NA,NA,NA,NA,NA,NA,NA,NA,849,849,animal_model,pedigree,no,narrow,authors,non_adult,adult,age at first egg,numbe of eggs laid from 77 to 110 days of age,reverse_maturation,fertility,include_2,cor,0.09,"[-0.27, 0.44]",95CI,NA,NA,NA,NA,NA,NA,model_c,table 4,maturation,fertility,pedigree,0.090244188,849,-1,-0.090244188,female,cross,Aves,between
481,Coturnix coturnix coturnix,357,rayyan-697472789,Searching for phenotypic causal networks involving complex traits: An application to European quail,2011,NA,NA,lab,both,female,NA,NA,NA,NA,NA,NA,NA,NA,849,849,animal_model,pedigree,no,narrow,authors,non_adult,adult,average egg weight from 77 to 110 days of age,numbe of eggs laid from 77 to 110 days of age,size,fertility,include_2,cor,0.05,"[-0.18, 0.29]",95CI,NA,NA,NA,NA,NA,NA,model_c,table 4,size,fertility,pedigree,0.050041729,849,1,0.050041729,female,cross,Aves,between
483,Crassostrea gigas,21,rayyan-687940442,"Genetic polymorphism and trade-offs in the early life-history strategy of the Pacific oyster, Crassostrea gigas (Thunberg, 1795): A quantitative genetic study",2003,NA,"Charente Maritime, France",lab,both,both,19,19,NA,NA,19,19,5,5,570,570,sire_mean_correlation,full/half_sib,no,narrow,authors,non_adult,non_adult,size at settlement,metamorphosis success,size,survival,include,cor,NA,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-687940442,table 6,size,survival,family,NA,19,1,NA,both,non_adult,Bivalvia,between
484,Crassostrea gigas,21,rayyan-687940442,"Genetic polymorphism and trade-offs in the early life-history strategy of the Pacific oyster, Crassostrea gigas (Thunberg, 1795): A quantitative genetic study",2003,NA,"Charente Maritime, France",lab,both,both,21,19,NA,NA,21,19,6,5,630,570,dam_mean_correlation,full/half_sib,no,broad,authors,non_adult,non_adult,larval growth rate,size at settlement,growth,size,include,cor,NA,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-687940442,table 6,growth,size,family,NA,19,1,NA,both,non_adult,Bivalvia,between
486,Crassostrea gigas,21,rayyan-687940442,"Genetic polymorphism and trade-offs in the early life-history strategy of the Pacific oyster, Crassostrea gigas (Thunberg, 1795): A quantitative genetic study",2003,NA,"Charente Maritime, France",lab,both,both,21,19,NA,NA,21,19,6,5,630,570,dam_mean_correlation,full/half_sib,no,broad,authors,non_adult,non_adult,larval development rate,size at settlement,maturation,size,include,cor,NA,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-687940442,table 6,maturation,size,family,NA,19,1,NA,both,non_adult,Bivalvia,between
487,Crassostrea gigas,21,rayyan-687940442,"Genetic polymorphism and trade-offs in the early life-history strategy of the Pacific oyster, Crassostrea gigas (Thunberg, 1795): A quantitative genetic study",2003,NA,"Charente Maritime, France",lab,both,both,19,19,NA,NA,19,19,5,5,570,570,dam_mean_correlation,full/half_sib,no,broad,authors,non_adult,non_adult,size at settlement,metamorphosis success,size,survival,include,cor,-0.46,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-687940442,table 6,size,survival,family,-0.497311288,19,1,-0.497311288,both,non_adult,Bivalvia,between
488,Crassostrea gigas,21,rayyan-687940442,"Genetic polymorphism and trade-offs in the early life-history strategy of the Pacific oyster, Crassostrea gigas (Thunberg, 1795): A quantitative genetic study",2003,NA,"Charente Maritime, France",lab,both,both,19,19,NA,NA,19,19,5,5,570,570,sire_mean_correlation,full/half_sib,no,narrow,authors,non_adult,adult,size at settlement,weight after metamorphosis,size,size,include,cor,NA,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-687940442,table 6,size,size,family,NA,19,1,NA,both,cross,Bivalvia,within
489,Crassostrea gigas,21,rayyan-687940442,"Genetic polymorphism and trade-offs in the early life-history strategy of the Pacific oyster, Crassostrea gigas (Thunberg, 1795): A quantitative genetic study",2003,NA,"Charente Maritime, France",lab,both,both,19,19,NA,NA,19,19,5,5,570,570,sire_mean_correlation,full/half_sib,no,narrow,authors,non_adult,non_adult,size at settlement,juvenile growth rate,size,growth,include,cor,NA,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-687940442,table 6,size,growth,family,NA,19,1,NA,both,non_adult,Bivalvia,between
490,Crassostrea gigas,21,rayyan-687940442,"Genetic polymorphism and trade-offs in the early life-history strategy of the Pacific oyster, Crassostrea gigas (Thunberg, 1795): A quantitative genetic study",2003,NA,"Charente Maritime, France",lab,both,both,21,19,NA,NA,21,19,6,5,630,570,dam_mean_correlation,full/half_sib,no,broad,authors,non_adult,non_adult,larval development rate,juvenile growth rate,maturation,growth,include,cor,NA,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-687940442,table 6,maturation,growth,family,NA,19,1,NA,both,non_adult,Bivalvia,between
491,Crassostrea gigas,21,rayyan-687940442,"Genetic polymorphism and trade-offs in the early life-history strategy of the Pacific oyster, Crassostrea gigas (Thunberg, 1795): A quantitative genetic study",2003,NA,"Charente Maritime, France",lab,both,both,19,19,NA,NA,19,19,5,5,570,570,dam_mean_correlation,full/half_sib,no,broad,authors,non_adult,non_adult,metamorphosis success,juvenile survival probability ,survival,survival,include,cor,-0.23,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-687940442,table 6,survival,survival,family,-0.234189467,19,1,-0.234189467,both,non_adult,Bivalvia,within
492,Crassostrea gigas,21,rayyan-687940442,"Genetic polymorphism and trade-offs in the early life-history strategy of the Pacific oyster, Crassostrea gigas (Thunberg, 1795): A quantitative genetic study",2003,NA,"Charente Maritime, France",lab,both,both,19,19,NA,NA,19,19,5,5,570,570,dam_mean_correlation,full/half_sib,no,broad,authors,non_adult,adult,metamorphosis success,weight after metamorphosis,survival,size,include,cor,-0.84,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-687940442,table 6,survival,size,family,-1.221173518,19,1,-1.221173518,both,cross,Bivalvia,between
493,Crassostrea gigas,21,rayyan-687940442,"Genetic polymorphism and trade-offs in the early life-history strategy of the Pacific oyster, Crassostrea gigas (Thunberg, 1795): A quantitative genetic study",2003,NA,"Charente Maritime, France",lab,both,both,19,19,NA,NA,19,19,5,5,570,570,dam_mean_correlation,full/half_sib,no,broad,authors,non_adult,non_adult,metamorphosis success,juvenile growth rate,survival,growth,include,cor,0.58,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-687940442,table 6,survival,growth,family,0.662462707,19,1,0.662462707,both,non_adult,Bivalvia,between
494,Crassostrea gigas,21,rayyan-687940442,"Genetic polymorphism and trade-offs in the early life-history strategy of the Pacific oyster, Crassostrea gigas (Thunberg, 1795): A quantitative genetic study",2003,NA,"Charente Maritime, France",lab,both,both,19,19,NA,NA,19,19,5,5,570,570,dam_mean_correlation,full/half_sib,no,broad,authors,non_adult,non_adult,size at settlement,juvenile growth rate,size,growth,include,cor,NA,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-687940442,table 6,size,growth,family,NA,19,1,NA,both,non_adult,Bivalvia,between
495,Crassostrea gigas,21,rayyan-687940442,"Genetic polymorphism and trade-offs in the early life-history strategy of the Pacific oyster, Crassostrea gigas (Thunberg, 1795): A quantitative genetic study",2003,NA,"Charente Maritime, France",lab,both,both,19,19,NA,NA,19,19,5,5,570,570,dam_mean_correlation,full/half_sib,no,broad,authors,non_adult,non_adult,juvenile survival probability ,juvenile growth rate,survival,growth,include,cor,0.13,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-687940442,table 6,survival,growth,family,0.13073985,19,1,0.13073985,both,non_adult,Bivalvia,between
496,Crassostrea gigas,21,rayyan-687940442,"Genetic polymorphism and trade-offs in the early life-history strategy of the Pacific oyster, Crassostrea gigas (Thunberg, 1795): A quantitative genetic study",2003,NA,"Charente Maritime, France",lab,both,both,19,19,NA,NA,19,19,5,5,570,570,dam_mean_correlation,full/half_sib,no,broad,authors,adult,non_adult,weight after metamorphosis,juvenile growth rate,size,growth,include,cor,NA,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-687940442,table 6,size,growth,family,NA,19,1,NA,both,cross,Bivalvia,between
497,Crassostrea gigas,21,rayyan-687940442,"Genetic polymorphism and trade-offs in the early life-history strategy of the Pacific oyster, Crassostrea gigas (Thunberg, 1795): A quantitative genetic study",2003,NA,"Charente Maritime, France",lab,both,both,21,19,NA,NA,21,19,6,5,630,570,dam_mean_correlation,full/half_sib,no,broad,authors,non_adult,non_adult,larval development rate,juvenile survival probability ,maturation,survival,include,cor,-0.15,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-687940442,table 6,maturation,survival,family,-0.151140436,19,1,-0.151140436,both,non_adult,Bivalvia,between
498,Crassostrea gigas,21,rayyan-687940442,"Genetic polymorphism and trade-offs in the early life-history strategy of the Pacific oyster, Crassostrea gigas (Thunberg, 1795): A quantitative genetic study",2003,NA,"Charente Maritime, France",lab,both,both,21,19,NA,NA,21,19,6,5,630,570,dam_mean_correlation,full/half_sib,no,broad,authors,non_adult,non_adult,larval development rate,metamorphosis success,maturation,survival,include,cor,-0.37,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-687940442,table 6,maturation,survival,family,-0.3884231,19,1,-0.3884231,both,non_adult,Bivalvia,between
499,Crassostrea gigas,21,rayyan-687940442,"Genetic polymorphism and trade-offs in the early life-history strategy of the Pacific oyster, Crassostrea gigas (Thunberg, 1795): A quantitative genetic study",2003,NA,"Charente Maritime, France",lab,both,both,21,19,NA,NA,21,19,6,5,630,570,sire_mean_correlation,full/half_sib,no,narrow,authors,non_adult,non_adult,larval survival probability ,metamorphosis success,survival,survival,include,cor,-0.54,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-687940442,table 6,survival,survival,family,-0.604155603,19,1,-0.604155603,both,non_adult,Bivalvia,within
500,Crassostrea gigas,21,rayyan-687940442,"Genetic polymorphism and trade-offs in the early life-history strategy of the Pacific oyster, Crassostrea gigas (Thunberg, 1795): A quantitative genetic study",2003,NA,"Charente Maritime, France",lab,both,both,21,19,NA,NA,21,19,6,5,630,570,sire_mean_correlation,full/half_sib,no,narrow,authors,non_adult,adult,larval survival probability ,weight after metamorphosis,survival,size,include,cor,-0.02,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-687940442,table 6,survival,size,family,-0.020002667,19,1,-0.020002667,both,cross,Bivalvia,between
501,Crassostrea gigas,21,rayyan-687940442,"Genetic polymorphism and trade-offs in the early life-history strategy of the Pacific oyster, Crassostrea gigas (Thunberg, 1795): A quantitative genetic study",2003,NA,"Charente Maritime, France",lab,both,both,21,19,NA,NA,21,19,6,5,630,570,sire_mean_correlation,full/half_sib,no,narrow,authors,non_adult,non_adult,larval survival probability ,juvenile growth rate,survival,growth,include,cor,0.16,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-687940442,table 6,survival,growth,family,0.161386696,19,1,0.161386696,both,non_adult,Bivalvia,between
502,Crassostrea gigas,21,rayyan-687940442,"Genetic polymorphism and trade-offs in the early life-history strategy of the Pacific oyster, Crassostrea gigas (Thunberg, 1795): A quantitative genetic study",2003,NA,"Charente Maritime, France",lab,both,both,21,19,NA,NA,21,19,6,5,630,570,sire_mean_correlation,full/half_sib,no,narrow,authors,non_adult,non_adult,larval survival probability ,size at settlement,survival,size,include,cor,0.34,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-687940442,table 6,survival,size,family,0.354092529,19,1,0.354092529,both,non_adult,Bivalvia,between
503,Crassostrea gigas,21,rayyan-687940442,"Genetic polymorphism and trade-offs in the early life-history strategy of the Pacific oyster, Crassostrea gigas (Thunberg, 1795): A quantitative genetic study",2003,NA,"Charente Maritime, France",lab,both,both,21,19,NA,NA,21,19,6,5,630,570,sire_mean_correlation,full/half_sib,no,narrow,authors,non_adult,non_adult,larval growth rate,metamorphosis success,growth,survival,include,cor,NA,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-687940442,table 6,growth,survival,family,NA,19,1,NA,both,non_adult,Bivalvia,between
504,Crassostrea gigas,21,rayyan-687940442,"Genetic polymorphism and trade-offs in the early life-history strategy of the Pacific oyster, Crassostrea gigas (Thunberg, 1795): A quantitative genetic study",2003,NA,"Charente Maritime, France",lab,both,both,21,19,NA,NA,21,19,6,5,630,570,sire_mean_correlation,full/half_sib,no,narrow,authors,non_adult,adult,larval growth rate,weight after metamorphosis,growth,size,include,cor,NA,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-687940442,table 6,growth,size,family,NA,19,1,NA,both,cross,Bivalvia,between
505,Crassostrea gigas,21,rayyan-687940442,"Genetic polymorphism and trade-offs in the early life-history strategy of the Pacific oyster, Crassostrea gigas (Thunberg, 1795): A quantitative genetic study",2003,NA,"Charente Maritime, France",lab,both,both,21,19,NA,NA,21,19,6,5,630,570,sire_mean_correlation,full/half_sib,no,narrow,authors,non_adult,non_adult,larval growth rate,juvenile growth rate,growth,growth,include,cor,NA,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-687940442,table 6,growth,growth,family,NA,19,1,NA,both,non_adult,Bivalvia,within
506,Crassostrea gigas,21,rayyan-687940442,"Genetic polymorphism and trade-offs in the early life-history strategy of the Pacific oyster, Crassostrea gigas (Thunberg, 1795): A quantitative genetic study",2003,NA,"Charente Maritime, France",lab,both,both,21,19,NA,NA,21,19,6,5,630,570,sire_mean_correlation,full/half_sib,no,narrow,authors,non_adult,non_adult,larval development rate,size at settlement,maturation,size,include,cor,NA,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-687940442,table 6,maturation,size,family,NA,19,1,NA,both,non_adult,Bivalvia,between
507,Crassostrea gigas,21,rayyan-687940442,"Genetic polymorphism and trade-offs in the early life-history strategy of the Pacific oyster, Crassostrea gigas (Thunberg, 1795): A quantitative genetic study",2003,NA,"Charente Maritime, France",lab,both,both,19,19,NA,NA,19,19,5,5,570,570,dam_mean_correlation,full/half_sib,no,broad,authors,non_adult,adult,juvenile survival probability ,weight after metamorphosis,survival,size,include,cor,-0.07,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-687940442,table 6,survival,size,family,-0.070114671,19,1,-0.070114671,both,cross,Bivalvia,between
508,Crassostrea gigas,21,rayyan-687940442,"Genetic polymorphism and trade-offs in the early life-history strategy of the Pacific oyster, Crassostrea gigas (Thunberg, 1795): A quantitative genetic study",2003,NA,"Charente Maritime, France",lab,both,both,21,19,NA,NA,21,19,6,5,630,570,sire_mean_correlation,full/half_sib,no,narrow,authors,non_adult,adult,larval development rate,weight after metamorphosis,maturation,size,include,cor,NA,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-687940442,table 6,maturation,size,family,NA,19,1,NA,both,cross,Bivalvia,between
509,Crassostrea gigas,21,rayyan-687940442,"Genetic polymorphism and trade-offs in the early life-history strategy of the Pacific oyster, Crassostrea gigas (Thunberg, 1795): A quantitative genetic study",2003,NA,"Charente Maritime, France",lab,both,both,21,19,NA,NA,21,19,6,5,630,570,sire_mean_correlation,full/half_sib,no,narrow,authors,non_adult,non_adult,larval development rate,juvenile growth rate,maturation,growth,include,cor,NA,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-687940442,table 6,maturation,growth,family,NA,19,1,NA,both,non_adult,Bivalvia,between
510,Crassostrea gigas,21,rayyan-687940442,"Genetic polymorphism and trade-offs in the early life-history strategy of the Pacific oyster, Crassostrea gigas (Thunberg, 1795): A quantitative genetic study",2003,NA,"Charente Maritime, France",lab,both,both,21,21,NA,NA,21,21,6,6,630,630,dam_mean_correlation,full/half_sib,no,broad,authors,non_adult,non_adult,larval survival probability ,larval growth rate,survival,growth,include,cor,0.89,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-687940442,table 6,survival,growth,family,1.421925871,21,1,1.421925871,both,non_adult,Bivalvia,between
511,Crassostrea gigas,21,rayyan-687940442,"Genetic polymorphism and trade-offs in the early life-history strategy of the Pacific oyster, Crassostrea gigas (Thunberg, 1795): A quantitative genetic study",2003,NA,"Charente Maritime, France",lab,both,both,21,21,NA,NA,21,21,6,6,630,630,dam_mean_correlation,full/half_sib,no,broad,authors,non_adult,non_adult,larval survival probability ,larval development rate,survival,maturation,include,cor,0.68,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-687940442,table 6,survival,maturation,family,0.829114038,21,1,0.829114038,both,non_adult,Bivalvia,between
512,Crassostrea gigas,21,rayyan-687940442,"Genetic polymorphism and trade-offs in the early life-history strategy of the Pacific oyster, Crassostrea gigas (Thunberg, 1795): A quantitative genetic study",2003,NA,"Charente Maritime, France",lab,both,both,21,19,NA,NA,21,19,6,5,630,570,dam_mean_correlation,full/half_sib,no,broad,authors,non_adult,non_adult,larval survival probability ,size at settlement,survival,size,include,cor,0.85,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-687940442,table 6,survival,size,family,1.256152812,19,1,1.256152812,both,non_adult,Bivalvia,between
513,Crassostrea gigas,21,rayyan-687940442,"Genetic polymorphism and trade-offs in the early life-history strategy of the Pacific oyster, Crassostrea gigas (Thunberg, 1795): A quantitative genetic study",2003,NA,"Charente Maritime, France",lab,both,both,19,19,NA,NA,19,19,5,5,570,570,sire_mean_correlation,full/half_sib,no,narrow,authors,non_adult,adult,metamorphosis success,weight after metamorphosis,survival,size,include,cor,NA,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-687940442,table 6,survival,size,family,NA,19,1,NA,both,cross,Bivalvia,between
514,Crassostrea gigas,21,rayyan-687940442,"Genetic polymorphism and trade-offs in the early life-history strategy of the Pacific oyster, Crassostrea gigas (Thunberg, 1795): A quantitative genetic study",2003,NA,"Charente Maritime, France",lab,both,both,19,19,NA,NA,19,19,5,5,570,570,sire_mean_correlation,full/half_sib,no,narrow,authors,non_adult,non_adult,metamorphosis success,juvenile growth rate,survival,growth,include,cor,NA,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-687940442,table 6,survival,growth,family,NA,19,1,NA,both,non_adult,Bivalvia,between
515,Crassostrea gigas,21,rayyan-687940442,"Genetic polymorphism and trade-offs in the early life-history strategy of the Pacific oyster, Crassostrea gigas (Thunberg, 1795): A quantitative genetic study",2003,NA,"Charente Maritime, France",lab,both,both,21,19,NA,NA,21,19,6,5,630,570,sire_mean_correlation,full/half_sib,no,narrow,authors,non_adult,non_adult,larval growth rate,size at settlement,growth,size,include,cor,NA,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-687940442,table 6,growth,size,family,NA,19,1,NA,both,non_adult,Bivalvia,between
516,Crassostrea gigas,21,rayyan-687940442,"Genetic polymorphism and trade-offs in the early life-history strategy of the Pacific oyster, Crassostrea gigas (Thunberg, 1795): A quantitative genetic study",2003,NA,"Charente Maritime, France",lab,both,both,19,19,NA,NA,19,19,5,5,570,570,dam_mean_correlation,full/half_sib,no,broad,authors,non_adult,adult,size at settlement,weight after metamorphosis,size,size,include,cor,NA,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-687940442,table 6,size,size,family,NA,19,1,NA,both,cross,Bivalvia,within
517,Crassostrea gigas,21,rayyan-687940442,"Genetic polymorphism and trade-offs in the early life-history strategy of the Pacific oyster, Crassostrea gigas (Thunberg, 1795): A quantitative genetic study",2003,NA,"Charente Maritime, France",lab,both,both,21,19,NA,NA,21,19,6,5,630,570,dam_mean_correlation,full/half_sib,no,broad,authors,non_adult,adult,larval survival probability ,weight after metamorphosis,survival,size,include,cor,0.57,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-687940442,table 6,survival,size,family,0.647522845,19,1,0.647522845,both,cross,Bivalvia,between
518,Crassostrea gigas,21,rayyan-687940442,"Genetic polymorphism and trade-offs in the early life-history strategy of the Pacific oyster, Crassostrea gigas (Thunberg, 1795): A quantitative genetic study",2003,NA,"Charente Maritime, France",lab,both,both,21,19,NA,NA,21,19,6,5,630,570,dam_mean_correlation,full/half_sib,no,broad,authors,non_adult,non_adult,larval survival probability ,juvenile growth rate,survival,growth,include,cor,-0.64,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-687940442,table 6,survival,growth,family,-0.758173745,19,1,-0.758173745,both,non_adult,Bivalvia,between
519,Crassostrea gigas,21,rayyan-687940442,"Genetic polymorphism and trade-offs in the early life-history strategy of the Pacific oyster, Crassostrea gigas (Thunberg, 1795): A quantitative genetic study",2003,NA,"Charente Maritime, France",lab,both,both,21,19,NA,NA,21,19,6,5,630,570,dam_mean_correlation,full/half_sib,no,broad,authors,non_adult,non_adult,larval growth rate,metamorphosis success,growth,survival,include,cor,-0.6,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-687940442,table 6,growth,survival,family,-0.693147181,19,1,-0.693147181,both,non_adult,Bivalvia,between
520,Crassostrea gigas,21,rayyan-687940442,"Genetic polymorphism and trade-offs in the early life-history strategy of the Pacific oyster, Crassostrea gigas (Thunberg, 1795): A quantitative genetic study",2003,NA,"Charente Maritime, France",lab,both,both,21,19,NA,NA,21,19,6,5,630,570,sire_mean_correlation,full/half_sib,no,narrow,authors,non_adult,non_adult,larval development rate,metamorphosis success,maturation,survival,include,cor,NA,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-687940442,table 6,maturation,survival,family,NA,19,1,NA,both,non_adult,Bivalvia,between
521,Crassostrea gigas,21,rayyan-687940442,"Genetic polymorphism and trade-offs in the early life-history strategy of the Pacific oyster, Crassostrea gigas (Thunberg, 1795): A quantitative genetic study",2003,NA,"Charente Maritime, France",lab,both,both,21,19,NA,NA,21,19,6,5,630,570,dam_mean_correlation,full/half_sib,no,broad,authors,non_adult,adult,larval growth rate,weight after metamorphosis,growth,size,include,cor,NA,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-687940442,table 6,growth,size,family,NA,19,1,NA,both,cross,Bivalvia,between
523,Crassostrea gigas,21,rayyan-687940442,"Genetic polymorphism and trade-offs in the early life-history strategy of the Pacific oyster, Crassostrea gigas (Thunberg, 1795): A quantitative genetic study",2003,NA,"Charente Maritime, France",lab,both,both,21,19,NA,NA,21,19,6,5,630,570,dam_mean_correlation,full/half_sib,no,broad,authors,non_adult,non_adult,larval growth rate,juvenile growth rate,growth,growth,include,cor,NA,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-687940442,table 6,growth,growth,family,NA,19,1,NA,both,non_adult,Bivalvia,within
525,Crassostrea gigas,21,rayyan-687940442,"Genetic polymorphism and trade-offs in the early life-history strategy of the Pacific oyster, Crassostrea gigas (Thunberg, 1795): A quantitative genetic study",2003,NA,"Charente Maritime, France",lab,both,both,21,21,NA,NA,21,21,6,6,630,630,sire_mean_correlation,full/half_sib,no,narrow,authors,non_adult,non_adult,larval survival probability ,larval development rate,survival,maturation,include,cor,0.45,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-687940442,table 6,survival,maturation,family,0.484700279,21,1,0.484700279,both,non_adult,Bivalvia,between
526,Crassostrea gigas,233,rayyan-197247355,"Plasticity in resource allocation based life history traits in the Pacific oyster, Crassostrea gigas. I. Spatial variation in food abundance",2004,1999,"Charente-Maritime, France",lab,both,both,15,15,NA,NA,15,15,5,5,681,3600,family_mean_correlation,full_sib,no,narrow,authors,both,both,mean growth,mean survival,growth,survival,include,cor,NA,0.68,se,NA,NA,NA,NA,NA,NA,experiment_1,table 5,growth,survival,family,NA,15,1,NA,both,both,Bivalvia,between
527,Crassostrea gigas,21,rayyan-687940442,"Genetic polymorphism and trade-offs in the early life-history strategy of the Pacific oyster, Crassostrea gigas (Thunberg, 1795): A quantitative genetic study",2003,NA,"Charente Maritime, France",lab,both,both,21,19,NA,NA,21,19,6,5,630,570,dam_mean_correlation,full/half_sib,no,broad,authors,non_adult,adult,larval development rate,weight after metamorphosis,maturation,size,include,cor,NA,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-687940442,table 6,maturation,size,family,NA,19,1,NA,both,cross,Bivalvia,between
528,Crassostrea gigas,21,rayyan-687940442,"Genetic polymorphism and trade-offs in the early life-history strategy of the Pacific oyster, Crassostrea gigas (Thunberg, 1795): A quantitative genetic study",2003,NA,"Charente Maritime, France",lab,both,both,19,19,NA,NA,19,19,5,5,570,570,dam_mean_correlation,full/half_sib,no,broad,authors,non_adult,non_adult,size at settlement,juvenile survival probability ,size,survival,include,cor,-0.79,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-687940442,table 6,size,survival,family,-1.071431684,19,1,-1.071431684,both,non_adult,Bivalvia,between
529,Crassostrea gigas,21,rayyan-687940442,"Genetic polymorphism and trade-offs in the early life-history strategy of the Pacific oyster, Crassostrea gigas (Thunberg, 1795): A quantitative genetic study",2003,NA,"Charente Maritime, France",lab,both,both,21,21,NA,NA,21,21,6,6,630,630,sire_mean_correlation,full/half_sib,no,narrow,authors,non_adult,non_adult,larval growth rate,larval development rate,growth,maturation,include,cor,NA,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-687940442,table 6,growth,maturation,family,NA,21,1,NA,both,non_adult,Bivalvia,between
530,Crassostrea gigas,21,rayyan-687940442,"Genetic polymorphism and trade-offs in the early life-history strategy of the Pacific oyster, Crassostrea gigas (Thunberg, 1795): A quantitative genetic study",2003,NA,"Charente Maritime, France",lab,both,both,19,19,NA,NA,19,19,5,5,570,570,sire_mean_correlation,full/half_sib,no,narrow,authors,adult,non_adult,weight after metamorphosis,juvenile growth rate,size,growth,include,cor,NA,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-687940442,table 6,size,growth,family,NA,19,1,NA,both,cross,Bivalvia,between
531,Crassostrea gigas,233,rayyan-197247355,"Plasticity in resource allocation based life history traits in the Pacific oyster, Crassostrea gigas. I. Spatial variation in food abundance",2004,1999,"Charente-Maritime, France",lab,both,both,15,15,NA,NA,15,15,5,5,900,6000,family_mean_correlation,full_sib,no,narrow,authors,both,both,mean growth,mean survival,growth,survival,include,cor,NA,0.67,se,NA,NA,NA,NA,NA,NA,experiment_2,table 5,growth,survival,family,NA,15,1,NA,both,both,Bivalvia,between
532,Crassostrea gigas,21,rayyan-687940442,"Genetic polymorphism and trade-offs in the early life-history strategy of the Pacific oyster, Crassostrea gigas (Thunberg, 1795): A quantitative genetic study",2003,NA,"Charente Maritime, France",lab,both,both,21,19,NA,NA,21,19,6,5,630,570,dam_mean_correlation,full/half_sib,no,broad,authors,non_adult,non_adult,larval growth rate,juvenile survival probability ,growth,survival,include,cor,0.09,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-687940442,table 6,growth,survival,family,0.090244188,19,1,0.090244188,both,non_adult,Bivalvia,between
533,Crassostrea gigas,21,rayyan-687940442,"Genetic polymorphism and trade-offs in the early life-history strategy of the Pacific oyster, Crassostrea gigas (Thunberg, 1795): A quantitative genetic study",2003,NA,"Charente Maritime, France",lab,both,both,21,21,NA,NA,21,21,6,6,630,630,dam_mean_correlation,full/half_sib,no,broad,authors,non_adult,non_adult,larval growth rate,larval development rate,growth,maturation,include,cor,NA,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-687940442,table 6,growth,maturation,family,NA,21,1,NA,both,non_adult,Bivalvia,between
535,Crassostrea gigas,21,rayyan-687940442,"Genetic polymorphism and trade-offs in the early life-history strategy of the Pacific oyster, Crassostrea gigas (Thunberg, 1795): A quantitative genetic study",2003,NA,"Charente Maritime, France",lab,both,both,21,19,NA,NA,21,19,6,5,630,570,dam_mean_correlation,full/half_sib,no,broad,authors,non_adult,non_adult,larval survival probability ,metamorphosis success,survival,survival,include,cor,-0.33,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-687940442,table 6,survival,survival,family,-0.342828254,19,1,-0.342828254,both,non_adult,Bivalvia,within
536,Crassostrea gigas,21,rayyan-687940442,"Genetic polymorphism and trade-offs in the early life-history strategy of the Pacific oyster, Crassostrea gigas (Thunberg, 1795): A quantitative genetic study",2003,NA,"Charente Maritime, France",lab,both,both,21,21,NA,NA,21,21,6,6,630,630,dam_mean_correlation,full/half_sib,no,broad,authors,non_adult,non_adult,larval survival probability ,larval growth rate,survival,growth,include,cor,0.55,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-687940442,table 6,survival,growth,family,0.618381314,21,1,0.618381314,both,non_adult,Bivalvia,between
537,Crassostrea gigas,21,rayyan-687940442,"Genetic polymorphism and trade-offs in the early life-history strategy of the Pacific oyster, Crassostrea gigas (Thunberg, 1795): A quantitative genetic study",2003,NA,"Charente Maritime, France",lab,both,both,21,19,NA,NA,21,19,6,5,630,570,dam_mean_correlation,full/half_sib,no,broad,authors,non_adult,non_adult,larval survival probability ,juvenile survival probability ,survival,survival,include,cor,-0.31,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-687940442,table 6,survival,survival,family,-0.320545409,19,1,-0.320545409,both,non_adult,Bivalvia,within
538,Cyanistes caeruleus ogliastrae,165,rayyan-197246997,Conserved G-matrices of morphological and life-history traits among continental and island blue tit populations,2017,1991–2014,France,field,both,both,NA,NA,NA,NA,NA,NA,NA,NA,1074,1074,animal_model,pedigree,no,narrow,authors,non_adult,adult,incubation time,clutch size,reverse_maturation,fertility,include,cov,0.052898705,"[-0.235, 0.2]",95CI,0.428,"[0.1941, 0.63]",95CI,0.855,"[0.363, 1.227]",95CI,D-Rouvière,table 3,maturation,fertility,pedigree,0.052948129,1074,-1,-0.052948129,both,cross,Aves,between
543,Cyanistes caeruleus ogliastrae,165,rayyan-197246997,Conserved G-matrices of morphological and life-history traits among continental and island blue tit populations,2017,1998–2014,Corsica,field,both,both,NA,NA,NA,NA,NA,NA,NA,NA,312,312,animal_model,pedigree,no,narrow,authors,non_adult,adult,incubation time,clutch size,reverse_maturation,fertility,include,cov,-0.162538835,"[-0.246, 0.096]",95CI,0.153,"[0.076, 0.295]",95CI,0.594,"[0.254, 1.131]",95CI,E-Muro,table 3,maturation,fertility,pedigree,-0.163993325,312,-1,0.163993325,both,cross,Aves,between
545,Cyanistes caeruleus ogliastrae,165,rayyan-197246997,Conserved G-matrices of morphological and life-history traits among continental and island blue tit populations,2017,1988–2014,Corsica,field,both,both,NA,NA,NA,NA,NA,NA,NA,NA,795,795,animal_model,pedigree,no,narrow,authors,non_adult,adult,incubation time,clutch size,reverse_maturation,fertility,include,cov,0.048942637,"[-0.115, 0.131]",95CI,0.109,"[0.069, 0.223]",95CI,0.383,"[0.224, 0.999]",95CI,E-Pirio,table 3,maturation,fertility,pedigree,0.048981772,795,-1,-0.048981772,both,cross,Aves,between
549,Cyanistes caeruleus ogliastrae,165,rayyan-197246997,Conserved G-matrices of morphological and life-history traits among continental and island blue tit populations,2017,1993–2014,Corsica,field,both,both,NA,NA,NA,NA,NA,NA,NA,NA,820,820,animal_model,pedigree,no,narrow,authors,non_adult,adult,incubation time,clutch size,reverse_maturation,fertility,include,cov,-0.077455478,"[-0.294, 0.201]",95CI,0.23,"[0.096, 0.374]",95CI,1.34,"[0.564, 1.981]",95CI,D-Muro,table 3,maturation,fertility,pedigree,-0.077610932,820,-1,0.077610932,both,cross,Aves,between
550,Daphnia magna,424,rayyan-697473407,Evolutionary genetics of aging in Daphnia,2005,1997,Moscow,lab,female,female,NA,NA,26,26,NA,NA,NA,NA,NA,NA,line_mean_correlation,genetic_line,no,broad,CC,adult,non_adult,fecundity at day 30,age at maturity,fertility,reverse_maturation,include,cor,0.234,NA,NA,NA,NA,NA,NA,NA,NA,mortality_16_20,table 2,fertility,maturation,genotype,0.238417017,26,-1,-0.238417017,female,cross,Branchiopoda,between
551,Daphnia magna,424,rayyan-697473407,Evolutionary genetics of aging in Daphnia,2005,1997,Moscow,lab,female,female,NA,NA,26,26,NA,NA,NA,NA,NA,NA,line_mean_correlation,genetic_line,no,broad,CC,adult,non_adult,fecundity at day 10,age at maturity,fertility,reverse_maturation,include,cor,0.555,NA,NA,NA,NA,NA,NA,NA,NA,mortality_1_15,table 2,fertility,maturation,genotype,0.625578271,26,-1,-0.625578271,female,cross,Branchiopoda,between
552,Daphnia magna,424,rayyan-697473407,Evolutionary genetics of aging in Daphnia,2005,1997,Moscow,lab,female,female,NA,NA,26,26,NA,NA,NA,NA,NA,NA,line_mean_correlation,genetic_line,no,broad,CC,non_adult,non_adult,age at first clutch,age at maturity,reverse_maturation,reverse_maturation,include,cor,-0.274,NA,NA,NA,NA,NA,NA,NA,NA,mortality_1_15,table 2,maturation,maturation,genotype,-0.281183411,26,1,-0.281183411,female,non_adult,Branchiopoda,within
553,Daphnia magna,424,rayyan-697473407,Evolutionary genetics of aging in Daphnia,2005,1997,Moscow,lab,female,female,NA,NA,25,25,NA,NA,NA,NA,NA,NA,line_mean_correlation,genetic_line,no,broad,CC,adult,non_adult,fecundity at day 10,age at maturity,fertility,reverse_maturation,include,cor,-0.277,NA,NA,NA,NA,NA,NA,NA,NA,mortality_31_45,table 2,fertility,maturation,genotype,-0.284429817,25,-1,0.284429817,female,cross,Branchiopoda,between
554,Daphnia magna,424,rayyan-697473407,Evolutionary genetics of aging in Daphnia,2005,1997,Moscow,lab,female,female,NA,NA,26,26,NA,NA,NA,NA,NA,NA,line_mean_correlation,genetic_line,no,broad,CC,adult,non_adult,"fecundity, mean of 1 and 2 clutches, cousins",age at maturity,fertility,reverse_maturation,include,cor,0.418,NA,NA,NA,NA,NA,NA,NA,NA,mortality_1_15,table 2,fertility,maturation,genotype,0.44526613,26,-1,-0.44526613,female,cross,Branchiopoda,between
555,Daphnia magna,424,rayyan-697473407,Evolutionary genetics of aging in Daphnia,2005,1997,Moscow,lab,female,female,NA,NA,26,26,NA,NA,NA,NA,NA,NA,line_mean_correlation,genetic_line,no,broad,CC,adult,non_adult,fecundity at day 10,age at maturity,fertility,reverse_maturation,include,cor,0.308,NA,NA,NA,NA,NA,NA,NA,NA,mortality_16_20,table 2,fertility,maturation,genotype,0.318334288,26,-1,-0.318334288,female,cross,Branchiopoda,between
556,Daphnia magna,424,rayyan-697473407,Evolutionary genetics of aging in Daphnia,2005,1997,Moscow,lab,female,female,NA,NA,24,24,NA,NA,NA,NA,NA,NA,line_mean_correlation,genetic_line,no,broad,CC,adult,non_adult,fecundity at day 30,age at maturity,fertility,reverse_maturation,include,cor,0.116,NA,NA,NA,NA,NA,NA,NA,NA,mortality_46_65,table 2,fertility,maturation,genotype,0.11652454,24,-1,-0.11652454,female,cross,Branchiopoda,between
557,Daphnia magna,424,rayyan-697473407,Evolutionary genetics of aging in Daphnia,2005,1997,Moscow,lab,female,female,NA,NA,24,24,NA,NA,NA,NA,NA,NA,line_mean_correlation,genetic_line,no,broad,CC,adult,non_adult,"fecundity, mean of 1 and 2 clutches, cousins",age at maturity,fertility,reverse_maturation,include,cor,0.043,NA,NA,NA,NA,NA,NA,NA,NA,mortality_46_65,table 2,fertility,maturation,genotype,0.043026532,24,-1,-0.043026532,female,cross,Branchiopoda,between
558,Daphnia magna,424,rayyan-697473407,Evolutionary genetics of aging in Daphnia,2005,1997,Moscow,lab,female,female,NA,NA,26,26,NA,NA,NA,NA,NA,NA,line_mean_correlation,genetic_line,no,broad,CC,adult,non_adult,"fecundity, mean of 1 and 2 clutches, cousins",age at maturity,fertility,reverse_maturation,include,cor,0.079,NA,NA,NA,NA,NA,NA,NA,NA,mortality_16_20,table 2,fertility,maturation,genotype,0.079164965,26,-1,-0.079164965,female,cross,Branchiopoda,between
559,Daphnia magna,424,rayyan-697473407,Evolutionary genetics of aging in Daphnia,2005,1997,Moscow,lab,female,female,NA,NA,26,26,NA,NA,NA,NA,NA,NA,line_mean_correlation,genetic_line,no,broad,CC,non_adult,non_adult,age at first clutch,age at maturity,reverse_maturation,reverse_maturation,include,cor,-0.02,NA,NA,NA,NA,NA,NA,NA,NA,mortality_16_20,table 2,maturation,maturation,genotype,-0.020002667,26,1,-0.020002667,female,non_adult,Branchiopoda,within
560,Daphnia magna,424,rayyan-697473407,Evolutionary genetics of aging in Daphnia,2005,1997,Moscow,lab,female,female,NA,NA,25,25,NA,NA,NA,NA,NA,NA,line_mean_correlation,genetic_line,no,broad,CC,non_adult,non_adult,age at first clutch,age at maturity,reverse_maturation,reverse_maturation,include,cor,-0.02,NA,NA,NA,NA,NA,NA,NA,NA,mortality_31_45,table 2,maturation,maturation,genotype,-0.020002667,25,1,-0.020002667,female,non_adult,Branchiopoda,within
561,Daphnia magna,424,rayyan-697473407,Evolutionary genetics of aging in Daphnia,2005,1997,Moscow,lab,female,female,NA,NA,24,24,NA,NA,NA,NA,NA,NA,line_mean_correlation,genetic_line,no,broad,CC,adult,non_adult,fecundity at day 10,age at maturity,fertility,reverse_maturation,include,cor,0.135,NA,NA,NA,NA,NA,NA,NA,NA,mortality_46_65,table 2,fertility,maturation,genotype,0.135829211,24,-1,-0.135829211,female,cross,Branchiopoda,between
562,Daphnia magna,424,rayyan-697473407,Evolutionary genetics of aging in Daphnia,2005,1997,Moscow,lab,female,female,NA,NA,26,26,NA,NA,NA,NA,NA,NA,line_mean_correlation,genetic_line,no,broad,CC,adult,non_adult,fecundity at day 30,age at maturity,fertility,reverse_maturation,include,cor,-0.13,NA,NA,NA,NA,NA,NA,NA,NA,mortality_1_15,table 2,fertility,maturation,genotype,-0.13073985,26,-1,0.13073985,female,cross,Branchiopoda,between
563,Daphnia magna,424,rayyan-697473407,Evolutionary genetics of aging in Daphnia,2005,1997,Moscow,lab,female,female,NA,NA,24,24,NA,NA,NA,NA,NA,NA,line_mean_correlation,genetic_line,no,broad,CC,non_adult,non_adult,age at first clutch,age at maturity,reverse_maturation,reverse_maturation,include,cor,0.231,NA,NA,NA,NA,NA,NA,NA,NA,mortality_46_65,table 2,maturation,maturation,genotype,0.235245578,24,1,0.235245578,female,non_adult,Branchiopoda,within
564,Daphnia magna,424,rayyan-697473407,Evolutionary genetics of aging in Daphnia,2005,1997,Moscow,lab,female,female,NA,NA,25,25,NA,NA,NA,NA,NA,NA,line_mean_correlation,genetic_line,no,broad,CC,adult,non_adult,"fecundity, mean of 1 and 2 clutches, cousins",age at maturity,fertility,reverse_maturation,include,cor,-0.087,NA,NA,NA,NA,NA,NA,NA,NA,mortality_31_45,table 2,fertility,maturation,genotype,-0.087220503,25,-1,0.087220503,female,cross,Branchiopoda,between
565,Daphnia magna,424,rayyan-697473407,Evolutionary genetics of aging in Daphnia,2005,1997,Moscow,lab,female,female,NA,NA,25,25,NA,NA,NA,NA,NA,NA,line_mean_correlation,genetic_line,no,broad,CC,adult,non_adult,fecundity at day 30,age at maturity,fertility,reverse_maturation,include,cor,-0.14,NA,NA,NA,NA,NA,NA,NA,NA,mortality_31_45,table 2,fertility,maturation,genotype,-0.140925576,25,-1,0.140925576,female,cross,Branchiopoda,between
566,Daphnia pulicaria,322,rayyan-697472523,Unexpected nongenetic individual heterogeneity and trait covariance in Daphnia and its consequences for ecological and evolutionary dynamics,2017,2011,"Round Lake, Ontario, Canada",lab,female,female,NA,NA,9,9,NA,NA,NA,NA,282,282,animal_model,genetic_line,no,broad,CC,adult,both,reproductive rate ,longevity,fertility,survival,include,cor,-0.17,"[0.873, -0.99]",95CI,NA,NA,NA,NA,NA,NA,cp_1000,figure 3,fertility,survival,genotype,-0.171666664,9,1,-0.171666664,female,cross,Branchiopoda,between
567,Daphnia pulicaria,322,rayyan-697472523,Unexpected nongenetic individual heterogeneity and trait covariance in Daphnia and its consequences for ecological and evolutionary dynamics,2017,2011,"Round Lake, Ontario, Canada",lab,female,female,NA,NA,9,9,NA,NA,NA,NA,285,285,animal_model,genetic_line,no,broad,CC,both,adult,growth ,reproductive rate ,growth,fertility,include,cor,0.306,"[0.988, -0.642]",95CI,NA,NA,NA,NA,NA,NA,cp_400,figure 3,growth,fertility,genotype,0.316126175,9,1,0.316126175,female,cross,Branchiopoda,between
568,Daphnia pulicaria,322,rayyan-697472523,Unexpected nongenetic individual heterogeneity and trait covariance in Daphnia and its consequences for ecological and evolutionary dynamics,2017,2011,"Round Lake, Ontario, Canada",lab,female,female,NA,NA,9,9,NA,NA,NA,NA,286,286,animal_model,genetic_line,no,broad,CC,both,both,growth ,longevity,growth,survival,include,cor,0.215,"[0.991, -0.864]",95CI,NA,NA,NA,NA,NA,NA,cp_800,figure 3,growth,survival,genotype,0.218407819,9,1,0.218407819,female,both,Branchiopoda,between
569,Daphnia pulicaria,322,rayyan-697472523,Unexpected nongenetic individual heterogeneity and trait covariance in Daphnia and its consequences for ecological and evolutionary dynamics,2017,2011,"Round Lake, Ontario, Canada",lab,female,female,NA,NA,9,9,NA,NA,NA,NA,382,382,animal_model,genetic_line,no,broad,CC,both,adult,growth ,reproductive rate ,growth,fertility,include,cor,-0.166,"[0.642, -0.921]",95CI,NA,NA,NA,NA,NA,NA,cp_200,figure 3,growth,fertility,genotype,-0.167550482,9,1,-0.167550482,female,cross,Branchiopoda,between
570,Daphnia pulicaria,322,rayyan-697472523,Unexpected nongenetic individual heterogeneity and trait covariance in Daphnia and its consequences for ecological and evolutionary dynamics,2017,2011,"Round Lake, Ontario, Canada",lab,female,female,NA,NA,9,9,NA,NA,NA,NA,282,282,animal_model,genetic_line,no,broad,CC,adult,both,reproductive rate ,longevity,fertility,survival,include,cor,-0.055,"[0.939, -0.968]",95CI,NA,NA,NA,NA,NA,NA,cp_600,figure 3,fertility,survival,genotype,-0.055055559,9,1,-0.055055559,female,cross,Branchiopoda,between
571,Daphnia pulicaria,322,rayyan-697472523,Unexpected nongenetic individual heterogeneity and trait covariance in Daphnia and its consequences for ecological and evolutionary dynamics,2017,2011,"Round Lake, Ontario, Canada",lab,female,female,NA,NA,9,9,NA,NA,NA,NA,282,282,animal_model,genetic_line,no,broad,CC,both,both,growth ,longevity,growth,survival,include,cor,0.118,"[0.973, -0.869]",95CI,NA,NA,NA,NA,NA,NA,cp_1000,figure 3,growth,survival,genotype,0.118552299,9,1,0.118552299,female,both,Branchiopoda,between
572,Daphnia pulicaria,322,rayyan-697472523,Unexpected nongenetic individual heterogeneity and trait covariance in Daphnia and its consequences for ecological and evolutionary dynamics,2017,2011,"Round Lake, Ontario, Canada",lab,female,female,NA,NA,9,9,NA,NA,NA,NA,285,285,animal_model,genetic_line,no,broad,CC,adult,both,reproductive rate ,longevity,fertility,survival,include,cor,0.226,"[1.021, -0.768]",95CI,NA,NA,NA,NA,NA,NA,cp_400,figure 3,fertility,survival,genotype,0.229970121,9,1,0.229970121,female,cross,Branchiopoda,between
573,Daphnia pulicaria,322,rayyan-697472523,Unexpected nongenetic individual heterogeneity and trait covariance in Daphnia and its consequences for ecological and evolutionary dynamics,2017,2011,"Round Lake, Ontario, Canada",lab,female,female,NA,NA,9,9,NA,NA,NA,NA,286,286,animal_model,genetic_line,no,broad,CC,adult,both,reproductive rate ,longevity,fertility,survival,include,cor,-0.169,"[0.869, -0.982]",95CI,NA,NA,NA,NA,NA,NA,cp_800,figure 3,fertility,survival,genotype,-0.170637083,9,1,-0.170637083,female,cross,Branchiopoda,between
574,Daphnia pulicaria,322,rayyan-697472523,Unexpected nongenetic individual heterogeneity and trait covariance in Daphnia and its consequences for ecological and evolutionary dynamics,2017,2011,"Round Lake, Ontario, Canada",lab,female,female,NA,NA,9,9,NA,NA,NA,NA,382,382,animal_model,genetic_line,no,broad,CC,both,both,growth ,longevity,growth,survival,include,cor,-0.027,"[0.802, -0.889]",95CI,NA,NA,NA,NA,NA,NA,cp_200,figure 3,growth,survival,genotype,-0.027006564,9,1,-0.027006564,female,both,Branchiopoda,between
575,Daphnia pulicaria,322,rayyan-697472523,Unexpected nongenetic individual heterogeneity and trait covariance in Daphnia and its consequences for ecological and evolutionary dynamics,2017,2011,"Round Lake, Ontario, Canada",lab,female,female,NA,NA,9,9,NA,NA,NA,NA,382,382,animal_model,genetic_line,no,broad,CC,adult,both,reproductive rate ,longevity,fertility,survival,include,cor,-0.593,"[0.283, -0.965]",95CI,NA,NA,NA,NA,NA,NA,cp_200,figure 3,fertility,survival,genotype,-0.682280562,9,1,-0.682280562,female,cross,Branchiopoda,between
576,Daphnia pulicaria,322,rayyan-697472523,Unexpected nongenetic individual heterogeneity and trait covariance in Daphnia and its consequences for ecological and evolutionary dynamics,2017,2011,"Round Lake, Ontario, Canada",lab,female,female,NA,NA,9,9,NA,NA,NA,NA,285,285,animal_model,genetic_line,no,broad,CC,both,both,growth ,longevity,growth,survival,include,cor,0.073,"[0.975, -0.92]",95CI,NA,NA,NA,NA,NA,NA,cp_400,figure 3,growth,survival,genotype,0.073130089,9,1,0.073130089,female,both,Branchiopoda,between
577,Daphnia pulicaria,322,rayyan-697472523,Unexpected nongenetic individual heterogeneity and trait covariance in Daphnia and its consequences for ecological and evolutionary dynamics,2017,2011,"Round Lake, Ontario, Canada",lab,female,female,NA,NA,9,9,NA,NA,NA,NA,282,282,animal_model,genetic_line,no,broad,CC,both,both,growth ,longevity,growth,survival,include,cor,0.088,"[0.983, -0.919]",95CI,NA,NA,NA,NA,NA,NA,cp_600,figure 3,growth,survival,genotype,0.088228219,9,1,0.088228219,female,both,Branchiopoda,between
578,Daphnia pulicaria,322,rayyan-697472523,Unexpected nongenetic individual heterogeneity and trait covariance in Daphnia and its consequences for ecological and evolutionary dynamics,2017,2011,"Round Lake, Ontario, Canada",lab,female,female,NA,NA,9,9,NA,NA,NA,NA,286,286,animal_model,genetic_line,no,broad,CC,both,adult,growth ,reproductive rate ,growth,fertility,include,cor,-0.751,"[0.143, -1.016]",95CI,NA,NA,NA,NA,NA,NA,cp_800,figure 3,growth,fertility,genotype,-0.975244718,9,1,-0.975244718,female,cross,Branchiopoda,between
579,Daphnia pulicaria,322,rayyan-697472523,Unexpected nongenetic individual heterogeneity and trait covariance in Daphnia and its consequences for ecological and evolutionary dynamics,2017,2011,"Round Lake, Ontario, Canada",lab,female,female,NA,NA,9,9,NA,NA,NA,NA,282,282,animal_model,genetic_line,no,broad,CC,both,adult,growth ,reproductive rate ,growth,fertility,include,cor,-0.14,"[0.926, -0.988]",95CI,NA,NA,NA,NA,NA,NA,cp_1000,figure 3,growth,fertility,genotype,-0.140925576,9,1,-0.140925576,female,cross,Branchiopoda,between
580,Daphnia pulicaria,322,rayyan-697472523,Unexpected nongenetic individual heterogeneity and trait covariance in Daphnia and its consequences for ecological and evolutionary dynamics,2017,2011,"Round Lake, Ontario, Canada",lab,female,female,NA,NA,9,9,NA,NA,NA,NA,282,282,animal_model,genetic_line,no,broad,CC,both,adult,growth ,reproductive rate ,growth,fertility,include,cor,-0.249,"[0.883, -1.004]",95CI,NA,NA,NA,NA,NA,NA,cp_600,figure 3,growth,fertility,genotype,-0.254346429,9,1,-0.254346429,female,cross,Branchiopoda,between
581,Dineura pulloir,397,rayyan-697473009,Seasonally varying diet quality and the quantitative genetics of development time and body size in birch feeding insects,2001,NA,Finland,lab,male,male,NA,NA,NA,NA,16,16,NA,NA,296,296,animal_model,full_sib,no,broad,authors,non_adult,non_adult,development time,final larval mass,reverse_maturation,size,include,cor,0.196,0.376,se,NA,NA,NA,NA,NA,NA,species_7_covariance,figure 2a,maturation,size,family,0.198569333,16,-1,-0.198569333,male,non_adult,Insecta,between
583,Drosophila aldrichi,15,rayyan-178530635,"GENETIC AND PHENOTYPIC VARIATION FOR FLIGHT ABILITY IN THE CACTOPHILIC DROSOPHILA SPECIES, D-ALDRICHI AND D-BUZZATII",1995,NA,"Dixalea, Australis",lab,both,both,195,195,13,13,195,195,195,195,1300,1300,line_mean_correlation,genetic_line,no,broad,CC,non_adult,adult,egg-to-adult development time,body weight at emergence,reverse_maturation,size,include,cor,0.801,0.137,se,NA,NA,NA,NA,NA,NA,rayyan-178530635,table 2,maturation,size,genotype,1.10139626,13,-1,-1.10139626,both,cross,Insecta,between
584,Drosophila aldrichi,15,rayyan-178530635,"GENETIC AND PHENOTYPIC VARIATION FOR FLIGHT ABILITY IN THE CACTOPHILIC DROSOPHILA SPECIES, D-ALDRICHI AND D-BUZZATII",1995,NA,"Dixalea, Australis",lab,both,both,195,195,13,13,195,195,195,195,1300,910,line_mean_correlation,genetic_line,no,broad,CC,non_adult,adult,egg-to-adult development time,thorax length at 10 day old,reverse_maturation,size,include,cor,0.542,0.24,se,NA,NA,NA,NA,NA,NA,rayyan-178530635,table 2,maturation,size,genotype,0.606983185,13,-1,-0.606983185,both,cross,Insecta,between
585,Drosophila aldrichi,15,rayyan-178530635,"GENETIC AND PHENOTYPIC VARIATION FOR FLIGHT ABILITY IN THE CACTOPHILIC DROSOPHILA SPECIES, D-ALDRICHI AND D-BUZZATII",1995,NA,"Dixalea, Australis",lab,both,both,195,195,13,13,195,195,195,195,1300,910,line_mean_correlation,genetic_line,no,broad,CC,adult,adult,body weight at emergence,thorax length at 10 day old,size,size,include,cor,0.701,0.245,se,NA,NA,NA,NA,NA,NA,rayyan-178530635,table 2,size,size,genotype,0.86926401,13,1,0.86926401,both,adult,Insecta,within
586,Drosophila buzzatii,15,rayyan-178530635,"GENETIC AND PHENOTYPIC VARIATION FOR FLIGHT ABILITY IN THE CACTOPHILIC DROSOPHILA SPECIES, D-ALDRICHI AND D-BUZZATII",1995,NA,"Dixalea, Australis",lab,both,both,150,150,15,15,150,150,150,150,1500,1500,line_mean_correlation,genetic_line,no,broad,CC,non_adult,adult,egg-to-adult development time,body weight at emergence,reverse_maturation,size,include,cor,0.904,0.343,se,NA,NA,NA,NA,NA,NA,rayyan-178530635,table 2,maturation,size,genotype,1.493682012,15,-1,-1.493682012,both,cross,Insecta,between
587,Drosophila buzzatii,38,rayyan-697471323,Pupal emergence pattern in cactophilic Drosophila and the effect of host plants,2018,NA,Northwestern Argentina ,lab,both,both,NA,NA,10,10,10,10,NA,NA,3085,3085,line_mean_correlation,genetic_line,no,broad,CC,non_adult,non_adult,larval viability (the proportion of adult survivors),development time from first instar larvae to emergence,survival,reverse_maturation,include,cor,0.141,NA,NA,NA,NA,NA,NA,NA,NA,Host_A_(trichocereus),table 4,survival,maturation,genotype,0.141945714,10,-1,-0.141945714,both,non_adult,Insecta,between
589,Drosophila buzzatii,38,rayyan-697471323,Pupal emergence pattern in cactophilic Drosophila and the effect of host plants,2018,NA,Northwestern Argentina ,lab,both,both,NA,NA,10,10,10,10,NA,NA,3085,3085,line_mean_correlation,genetic_line,no,broad,CC,non_adult,adult,development time from first instar larvae to emergence,adult wing size,reverse_maturation,size,include,cor,0.109,NA,NA,NA,NA,NA,NA,NA,NA,Host_A_(trichocereus),table 4,maturation,size,genotype,0.10943478,10,-1,-0.10943478,both,cross,Insecta,between
591,Drosophila buzzatii,38,rayyan-697471323,Pupal emergence pattern in cactophilic Drosophila and the effect of host plants,2018,NA,Northwestern Argentina ,lab,both,both,NA,NA,10,10,10,10,NA,NA,3085,3085,line_mean_correlation,genetic_line,no,broad,CC,non_adult,adult,larval viability (the proportion of adult survivors),adult wing size,survival,size,include,cor,-0.044,NA,NA,NA,NA,NA,NA,NA,NA,Host_A_(trichocereus),table 4,survival,size,genotype,-0.044028428,10,1,-0.044028428,both,cross,Insecta,between
592,Drosophila buzzatii,38,rayyan-697471323,Pupal emergence pattern in cactophilic Drosophila and the effect of host plants,2018,NA,Northwestern Argentina ,lab,both,both,NA,NA,10,10,10,10,NA,NA,3085,3085,line_mean_correlation,genetic_line,no,broad,CC,non_adult,non_adult,larval viability (the proportion of adult survivors),development time from first instar larvae to emergence,survival,reverse_maturation,include,cor,0.355,NA,NA,NA,NA,NA,NA,NA,NA,Host_B_(opuntia),table 4,survival,maturation,genotype,0.371153208,10,-1,-0.371153208,both,non_adult,Insecta,between
597,Drosophila buzzatii,306,rayyan-197247966,Antagonistic pleiotropic effect of second-chromosome inversions on body size and early life-history traits in Drosophila buzzatii,1998,1990,"Carboneras and Collera, Spain",lab,male,male,NA,NA,10,10,NA,NA,NA,NA,NA,NA,line_mean_correlation,genetic_line,no,broad,authors,non_adult,adult,development time,thorax length,reverse_maturation,size,include,cor,0.174,NA,NA,NA,NA,NA,NA,NA,NA,karyotypic_male,4th para in result experiment a,maturation,size,genotype,0.175788613,10,-1,-0.175788613,male,cross,Insecta,between
598,Drosophila buzzatii,306,rayyan-197247966,Antagonistic pleiotropic effect of second-chromosome inversions on body size and early life-history traits in Drosophila buzzatii,1998,1990,"Carboneras and Collera, Spain",lab,female,female,NA,NA,10,10,NA,NA,NA,NA,NA,NA,matrix,genetic_line,no,narrow,authors,non_adult,adult,development time,thorax length,reverse_maturation,size,include,cor,0.574,NA,NA,NA,NA,NA,NA,NA,NA,additive_female,4th para in result experiment a,maturation,size,genotype,0.653468041,10,-1,-0.653468041,female,cross,Insecta,between
599,Drosophila buzzatii,248,rayyan-197247425,A genetic analysis of the relationship between life-history variation and heat-shock tolerance in Drosophila buzzatii,1999,NA,NA,lab,male,male,NA,NA,100,100,NA,NA,NA,NA,800,16000,line_mean_correlation,genetic_line,no,broad,CC,adult,non_adult,adult fecundity,larval survival,fertility,survival,include,cor,-0.22,0.1,se,NA,NA,NA,NA,NA,NA,male,figure 1,fertility,survival,genotype,-0.223656109,100,1,-0.223656109,male,cross,Insecta,between
600,Drosophila buzzatii,306,rayyan-197247966,Antagonistic pleiotropic effect of second-chromosome inversions on body size and early life-history traits in Drosophila buzzatii,1998,1990,"Carboneras and Collera, Spain",lab,female,female,NA,NA,10,10,NA,NA,NA,NA,NA,NA,line_mean_correlation,genetic_line,no,broad,authors,non_adult,adult,development time,thorax length,reverse_maturation,size,include,cor,0.792,NA,NA,NA,NA,NA,NA,NA,NA,karyotypic_female,4th para in result experiment a,maturation,size,genotype,1.076774757,10,-1,-1.076774757,female,cross,Insecta,between
601,Drosophila buzzatii,248,rayyan-197247425,A genetic analysis of the relationship between life-history variation and heat-shock tolerance in Drosophila buzzatii,1999,NA,NA,lab,male,male,NA,NA,100,100,NA,NA,NA,NA,16000,10000,line_mean_correlation,genetic_line,no,broad,CC,non_adult,both,development time,adult longevity,reverse_maturation,survival,include,cor,0.22,0.11,se,NA,NA,NA,NA,NA,NA,male,figure 1,maturation,survival,genotype,0.223656109,100,-1,-0.223656109,male,cross,Insecta,between
602,Drosophila buzzatii,38,rayyan-697471323,Pupal emergence pattern in cactophilic Drosophila and the effect of host plants,2018,NA,Northwestern Argentina ,lab,both,both,NA,NA,10,10,10,10,NA,NA,3085,3085,line_mean_correlation,genetic_line,no,broad,CC,non_adult,adult,larval viability (the proportion of adult survivors),adult wing size,survival,size,include,cor,-0.219,NA,NA,NA,NA,NA,NA,NA,NA,Host_B_(opuntia),table 4,survival,size,genotype,-0.22260549,10,1,-0.22260549,both,cross,Insecta,between
603,Drosophila buzzatii,15,rayyan-178530635,"GENETIC AND PHENOTYPIC VARIATION FOR FLIGHT ABILITY IN THE CACTOPHILIC DROSOPHILA SPECIES, D-ALDRICHI AND D-BUZZATII",1995,NA,"Dixalea, Australis",lab,both,both,150,150,15,15,150,150,150,150,1500,1050,line_mean_correlation,genetic_line,no,broad,CC,non_adult,adult,egg-to-adult development time,thorax length at 10 day old,reverse_maturation,size,include,cor,0.548,0.912,se,NA,NA,NA,NA,NA,NA,rayyan-178530635,table 2,maturation,size,genotype,0.615518437,15,-1,-0.615518437,both,cross,Insecta,between
604,Drosophila buzzatii,248,rayyan-197247425,A genetic analysis of the relationship between life-history variation and heat-shock tolerance in Drosophila buzzatii,1999,NA,NA,lab,female,female,NA,NA,100,100,NA,NA,NA,NA,16000,10000,line_mean_correlation,genetic_line,no,broad,CC,non_adult,both,development time,adult longevity,reverse_maturation,survival,include,cor,0.24,0.16,se,NA,NA,NA,NA,NA,NA,female,figure 1,maturation,survival,genotype,0.244774113,100,-1,-0.244774113,female,cross,Insecta,between
605,Drosophila buzzatii,15,rayyan-178530635,"GENETIC AND PHENOTYPIC VARIATION FOR FLIGHT ABILITY IN THE CACTOPHILIC DROSOPHILA SPECIES, D-ALDRICHI AND D-BUZZATII",1995,NA,"Dixalea, Australis",lab,both,both,150,150,15,15,150,150,150,150,1500,1050,line_mean_correlation,genetic_line,no,broad,CC,adult,adult,body weight at emergence,thorax length at 10 day old,size,size,include,cor,0.944,0.034,se,NA,NA,NA,NA,NA,NA,rayyan-178530635,table 2,size,size,genotype,1.773575647,15,1,1.773575647,both,adult,Insecta,within
606,Drosophila buzzatii,248,rayyan-197247425,A genetic analysis of the relationship between life-history variation and heat-shock tolerance in Drosophila buzzatii,1999,NA,NA,lab,male,male,NA,NA,100,100,NA,NA,NA,NA,800,16000,line_mean_correlation,genetic_line,no,broad,CC,adult,non_adult,adult fecundity,development time,fertility,reverse_maturation,include,cor,-0.22,0.02,se,NA,NA,NA,NA,NA,NA,male,figure 1,fertility,maturation,genotype,-0.223656109,100,-1,0.223656109,male,cross,Insecta,between
607,Drosophila buzzatii,248,rayyan-197247425,A genetic analysis of the relationship between life-history variation and heat-shock tolerance in Drosophila buzzatii,1999,NA,NA,lab,female,female,NA,NA,100,100,NA,NA,NA,NA,800,16000,line_mean_correlation,genetic_line,no,broad,CC,adult,non_adult,adult fecundity,larval survival,fertility,survival,include,cor,-0.11,0.08,se,NA,NA,NA,NA,NA,NA,female,figure 1,fertility,survival,genotype,-0.110446916,100,1,-0.110446916,female,cross,Insecta,between
608,Drosophila buzzatii,38,rayyan-697471323,Pupal emergence pattern in cactophilic Drosophila and the effect of host plants,2018,NA,Northwestern Argentina ,lab,both,both,NA,NA,10,10,10,10,NA,NA,3085,3085,line_mean_correlation,genetic_line,no,broad,CC,non_adult,adult,development time from first instar larvae to emergence,adult wing size,reverse_maturation,size,include,cor,-0.345,NA,NA,NA,NA,NA,NA,NA,NA,Host_B_(opuntia),table 4,maturation,size,genotype,-0.359757028,10,-1,0.359757028,both,cross,Insecta,between
609,Drosophila buzzatii,248,rayyan-197247425,A genetic analysis of the relationship between life-history variation and heat-shock tolerance in Drosophila buzzatii,1999,NA,NA,lab,female,female,NA,NA,100,100,NA,NA,NA,NA,800,16000,line_mean_correlation,genetic_line,no,broad,CC,adult,non_adult,adult fecundity,development time,fertility,reverse_maturation,include,cor,-0.2,0.03,se,NA,NA,NA,NA,NA,NA,female,figure 1,fertility,maturation,genotype,-0.202732554,100,-1,0.202732554,female,cross,Insecta,between
610,Drosophila buzzatii,248,rayyan-197247425,A genetic analysis of the relationship between life-history variation and heat-shock tolerance in Drosophila buzzatii,1999,NA,NA,lab,female,female,NA,NA,100,100,NA,NA,NA,NA,10000,16000,line_mean_correlation,genetic_line,no,broad,CC,both,non_adult,adult longevity,larval survival,survival,survival,include,cor,0.13,0.04,se,NA,NA,NA,NA,NA,NA,female,figure 1,survival,survival,genotype,0.13073985,100,1,0.13073985,female,cross,Insecta,within
611,Drosophila buzzatii,248,rayyan-197247425,A genetic analysis of the relationship between life-history variation and heat-shock tolerance in Drosophila buzzatii,1999,NA,NA,lab,male,male,NA,NA,100,100,NA,NA,NA,NA,10000,16000,line_mean_correlation,genetic_line,no,broad,CC,both,non_adult,adult longevity,larval survival,survival,survival,include,cor,0.23,0.07,se,NA,NA,NA,NA,NA,NA,male,figure 1,survival,survival,genotype,0.234189467,100,1,0.234189467,male,cross,Insecta,within
612,Drosophila koepferae,38,rayyan-697471323,Pupal emergence pattern in cactophilic Drosophila and the effect of host plants,2018,NA,Northwestern Argentina ,lab,both,both,NA,NA,10,10,10,10,NA,NA,3085,3085,line_mean_correlation,genetic_line,no,broad,CC,non_adult,adult,larval viability (the proportion of adult survivors),adult wing size,survival,size,include,cor,-0.162,NA,NA,NA,NA,NA,NA,NA,NA,Host_A_(trichocereus),table 4,survival,size,genotype,-0.163439918,10,1,-0.163439918,both,cross,Insecta,between
613,Drosophila koepferae,38,rayyan-697471323,Pupal emergence pattern in cactophilic Drosophila and the effect of host plants,2018,NA,Northwestern Argentina ,lab,both,both,NA,NA,10,10,10,10,NA,NA,3085,3085,line_mean_correlation,genetic_line,no,broad,CC,non_adult,non_adult,larval viability (the proportion of adult survivors),development time from first instar larvae to emergence,survival,reverse_maturation,include,cor,0.376,NA,NA,NA,NA,NA,NA,NA,NA,Host_B_(opuntia),table 4,survival,maturation,genotype,0.395392825,10,-1,-0.395392825,both,non_adult,Insecta,between
614,Drosophila koepferae,38,rayyan-697471323,Pupal emergence pattern in cactophilic Drosophila and the effect of host plants,2018,NA,Northwestern Argentina ,lab,both,both,NA,NA,10,10,10,10,NA,NA,3085,3085,line_mean_correlation,genetic_line,no,broad,CC,non_adult,adult,larval viability (the proportion of adult survivors),adult wing size,survival,size,include,cor,-0.157,NA,NA,NA,NA,NA,NA,NA,NA,Host_B_(opuntia),table 4,survival,size,genotype,-0.158309385,10,1,-0.158309385,both,cross,Insecta,between
615,Drosophila koepferae,38,rayyan-697471323,Pupal emergence pattern in cactophilic Drosophila and the effect of host plants,2018,NA,Northwestern Argentina ,lab,both,both,NA,NA,10,10,10,10,NA,NA,3085,3085,line_mean_correlation,genetic_line,no,broad,CC,non_adult,non_adult,larval viability (the proportion of adult survivors),development time from first instar larvae to emergence,survival,reverse_maturation,include,cor,0.351,NA,NA,NA,NA,NA,NA,NA,NA,Host_A_(trichocereus),table 4,survival,maturation,genotype,0.366583811,10,-1,-0.366583811,both,non_adult,Insecta,between
620,Drosophila koepferae,38,rayyan-697471323,Pupal emergence pattern in cactophilic Drosophila and the effect of host plants,2018,NA,Northwestern Argentina ,lab,both,both,NA,NA,10,10,10,10,NA,NA,3085,3085,line_mean_correlation,genetic_line,no,broad,CC,non_adult,adult,development time from first instar larvae to emergence,adult wing size,reverse_maturation,size,include,cor,-0.131,NA,NA,NA,NA,NA,NA,NA,NA,Host_A_(trichocereus),table 4,maturation,size,genotype,-0.131757175,10,-1,0.131757175,both,cross,Insecta,between
621,Drosophila koepferae,38,rayyan-697471323,Pupal emergence pattern in cactophilic Drosophila and the effect of host plants,2018,NA,Northwestern Argentina ,lab,both,both,NA,NA,10,10,10,10,NA,NA,3085,3085,line_mean_correlation,genetic_line,no,broad,CC,non_adult,adult,development time from first instar larvae to emergence,adult wing size,reverse_maturation,size,include,cor,-0.093,NA,NA,NA,NA,NA,NA,NA,NA,Host_B_(opuntia),table 4,maturation,size,genotype,-0.093269519,10,-1,0.093269519,both,cross,Insecta,between
626,Drosophila melanogaster,39,rayyan-697471325,Female life-history trade-offs and the maintenance of genetic variation in Drosophila melanogaster,2018,NA,NA,lab,female,female,NA,NA,26,26,NA,NA,NA,NA,1300,1300,line_mean_correlation,genetic_line,no,broad,CC,adult,adult,midlife offspring production as number of emerged offspring (at 3 week),early-life offspring production as number of emerged offspring (at 1 week),fertility,fertility,include,cor,0.47,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-697471325,table a2,fertility,fertility,genotype,0.510070337,26,1,0.510070337,female,adult,Insecta,within
627,Drosophila melanogaster,39,rayyan-697471325,Female life-history trade-offs and the maintenance of genetic variation in Drosophila melanogaster,2018,NA,NA,lab,female,female,NA,NA,26,26,NA,NA,NA,NA,1300,1300,line_mean_correlation,genetic_line,no,broad,CC,adult,adult,late-life offspring production as number of emerged offspring (at 5 week),early-life offspring production as number of emerged offspring (at 1 week),fertility,fertility,include,cor,0.56,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-697471325,table a2,fertility,fertility,genotype,0.632833187,26,1,0.632833187,female,adult,Insecta,within
634,Drosophila melanogaster,39,rayyan-697471325,Female life-history trade-offs and the maintenance of genetic variation in Drosophila melanogaster,2018,NA,NA,lab,female,female,NA,NA,26,31,NA,NA,NA,NA,1300,1550,line_mean_correlation,genetic_line,no,broad,CC,adult,both,early-life offspring production as number of emerged offspring (at 1 week),female longevity in the presence of males,fertility,survival,include,cor,0.27,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-697471325,table a2,fertility,survival,genotype,0.276863823,26,1,0.276863823,female,cross,Insecta,between
637,Drosophila melanogaster,39,rayyan-697471325,Female life-history trade-offs and the maintenance of genetic variation in Drosophila melanogaster,2018,NA,NA,lab,female,female,NA,NA,26,31,NA,NA,NA,NA,1300,1550,line_mean_correlation,genetic_line,no,broad,CC,adult,both,early-life offspring production as number of emerged offspring (at 1 week),female virgin longevity,fertility,survival,include,cor,0.14,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-697471325,table a2,fertility,survival,genotype,0.140925576,26,1,0.140925576,female,cross,Insecta,between
643,Drosophila melanogaster,46,rayyan-697471387,Spatially varying selection shapes life history clines among populations of Drosophila melanogaster from sub-Saharan Africa,2015,2002-2011,tropical and subtropical sub-Saharan populations,lab,female,female,NA,NA,22,39,NA,NA,NA,NA,285,230,line_mean_correlation,genetic_line,no,broad,CC,adult,adult,thorax length of 1 to 3 day odd adult females,fecundity 1-5 days (number of egg laid),size,fertility,include_2,cor,0.52,NA,NA,NA,NA,NA,NA,NA,NA,"above-equator (pop EF, ED, CO, EA, NG)",table s6,size,fertility,genotype,0.576339755,22,1,0.576339755,female,adult,Insecta,between
644,Drosophila melanogaster,46,rayyan-697471387,Spatially varying selection shapes life history clines among populations of Drosophila melanogaster from sub-Saharan Africa,2015,2002-2011,tropical and subtropical sub-Saharan populations,lab,female,female,NA,NA,22,39,NA,NA,NA,NA,285,200,line_mean_correlation,genetic_line,no,broad,CC,adult,adult,thorax length of 1 to 3 day odd adult females,fecundity 6-10 days (number of egg laid),size,fertility,include_2,cor,-0.08,NA,NA,NA,NA,NA,NA,NA,NA,"above-equator (pop EF, ED, CO, EA, NG)",table s6,size,fertility,genotype,-0.080171325,22,1,-0.080171325,female,adult,Insecta,between
645,Drosophila melanogaster,46,rayyan-697471387,Spatially varying selection shapes life history clines among populations of Drosophila melanogaster from sub-Saharan Africa,2015,2002-2011,tropical and subtropical sub-Saharan populations,lab,female,female,NA,NA,22,39,NA,NA,NA,NA,285,200,line_mean_correlation,genetic_line,no,broad,CC,adult,adult,thorax length of 1 to 3 day odd adult females,fecundity 1-10 days (number of eggs laid),size,fertility,include_2,cor,0.2,NA,NA,NA,NA,NA,NA,NA,NA,"above-equator (pop EF, ED, CO, EA, NG)",table s6,size,fertility,genotype,0.202732554,22,1,0.202732554,female,adult,Insecta,between
646,Drosophila melanogaster,46,rayyan-697471387,Spatially varying selection shapes life history clines among populations of Drosophila melanogaster from sub-Saharan Africa,2015,2002-2011,tropical and subtropical sub-Saharan populations,lab,female,female,NA,NA,22,39,NA,NA,NA,NA,285,233,line_mean_correlation,genetic_line,no,broad,CC,adult,both,thorax length of 1 to 3 day odd adult females,lifespan of female,size,survival,include_2,cor,-0.1,NA,NA,NA,NA,NA,NA,NA,NA,"above-equator (pop EF, ED, CO, EA, NG)",table s6,size,survival,genotype,-0.100335348,22,1,-0.100335348,female,cross,Insecta,between
647,Drosophila melanogaster,46,rayyan-697471387,Spatially varying selection shapes life history clines among populations of Drosophila melanogaster from sub-Saharan Africa,2015,2002-2011,tropical and subtropical sub-Saharan populations,lab,female,both,NA,NA,22,38,NA,NA,NA,NA,285,2265,line_mean_correlation,genetic_line,no,broad,CC,adult,non_adult,thorax length of 1 to 3 day odd adult females,proportion egg-to-adult survival (viability),size,survival,include_2,cor,-0.1,NA,NA,NA,NA,NA,NA,NA,NA,"above-equator (pop EF, ED, CO, EA, NG)",table s6,size,survival,genotype,-0.100335348,22,1,-0.100335348,female,cross,Insecta,between
648,Drosophila melanogaster,46,rayyan-697471387,Spatially varying selection shapes life history clines among populations of Drosophila melanogaster from sub-Saharan Africa,2015,2002-2011,tropical and subtropical sub-Saharan populations,lab,female,female,NA,NA,39,39,NA,NA,NA,NA,230,200,line_mean_correlation,genetic_line,no,broad,CC,adult,adult,fecundity 1-5 days (number of egg laid),fecundity 6-10 days (number of egg laid),fertility,fertility,include_2,cor,0.63,NA,NA,NA,NA,NA,NA,NA,NA,"above-equator (pop EF, ED, CO, EA, NG)",table s6,fertility,fertility,genotype,0.741416144,39,1,0.741416144,female,adult,Insecta,within
649,Drosophila melanogaster,46,rayyan-697471387,Spatially varying selection shapes life history clines among populations of Drosophila melanogaster from sub-Saharan Africa,2015,2002-2011,tropical and subtropical sub-Saharan populations,lab,female,female,NA,NA,39,39,NA,NA,NA,NA,230,200,line_mean_correlation,genetic_line,no,broad,CC,adult,adult,fecundity 1-5 days (number of egg laid),fecundity 1-10 days (number of eggs laid),fertility,fertility,include_2,cor,0.84,NA,NA,NA,NA,NA,NA,NA,NA,"above-equator (pop EF, ED, CO, EA, NG)",table s6,fertility,fertility,genotype,1.221173518,39,1,1.221173518,female,adult,Insecta,within
658,Drosophila melanogaster,46,rayyan-697471387,Spatially varying selection shapes life history clines among populations of Drosophila melanogaster from sub-Saharan Africa,2015,2002-2011,tropical and subtropical sub-Saharan populations,lab,female,female,NA,NA,14,22,NA,NA,NA,NA,191,128,line_mean_correlation,genetic_line,no,broad,CC,adult,adult,thorax length of 1 to 3 day odd adult females,fecundity 1-5 days (number of egg laid),size,fertility,include_2,cor,-0.05,NA,NA,NA,NA,NA,NA,NA,NA,"at-equator (pop RG, GA)",table s6,size,fertility,genotype,-0.050041729,14,1,-0.050041729,female,adult,Insecta,between
659,Drosophila melanogaster,46,rayyan-697471387,Spatially varying selection shapes life history clines among populations of Drosophila melanogaster from sub-Saharan Africa,2015,2002-2011,tropical and subtropical sub-Saharan populations,lab,female,female,NA,NA,14,22,NA,NA,NA,NA,191,128,line_mean_correlation,genetic_line,no,broad,CC,adult,adult,thorax length of 1 to 3 day odd adult females,fecundity 6-10 days (number of egg laid),size,fertility,include_2,cor,0.14,NA,NA,NA,NA,NA,NA,NA,NA,"at-equator (pop RG, GA)",table s6,size,fertility,genotype,0.140925576,14,1,0.140925576,female,adult,Insecta,between
660,Drosophila melanogaster,46,rayyan-697471387,Spatially varying selection shapes life history clines among populations of Drosophila melanogaster from sub-Saharan Africa,2015,2002-2011,tropical and subtropical sub-Saharan populations,lab,female,female,NA,NA,14,22,NA,NA,NA,NA,191,128,line_mean_correlation,genetic_line,no,broad,CC,adult,adult,thorax length of 1 to 3 day odd adult females,fecundity 1-10 days (number of eggs laid),size,fertility,include_2,cor,0.05,NA,NA,NA,NA,NA,NA,NA,NA,"at-equator (pop RG, GA)",table s6,size,fertility,genotype,0.050041729,14,1,0.050041729,female,adult,Insecta,between
661,Drosophila melanogaster,46,rayyan-697471387,Spatially varying selection shapes life history clines among populations of Drosophila melanogaster from sub-Saharan Africa,2015,2002-2011,tropical and subtropical sub-Saharan populations,lab,female,female,NA,NA,14,22,NA,NA,NA,NA,191,130,line_mean_correlation,genetic_line,no,broad,CC,adult,both,thorax length of 1 to 3 day odd adult females,lifespan of female,size,survival,include_2,cor,-0.03,NA,NA,NA,NA,NA,NA,NA,NA,"at-equator (pop RG, GA)",table s6,size,survival,genotype,-0.030009005,14,1,-0.030009005,female,cross,Insecta,between
662,Drosophila melanogaster,46,rayyan-697471387,Spatially varying selection shapes life history clines among populations of Drosophila melanogaster from sub-Saharan Africa,2015,2002-2011,tropical and subtropical sub-Saharan populations,lab,female,both,NA,NA,14,15,NA,NA,NA,NA,191,1050,line_mean_correlation,genetic_line,no,broad,CC,adult,non_adult,thorax length of 1 to 3 day odd adult females,proportion egg-to-adult survival (viability),size,survival,include_2,cor,0.14,NA,NA,NA,NA,NA,NA,NA,NA,"at-equator (pop RG, GA)",table s6,size,survival,genotype,0.140925576,14,1,0.140925576,female,cross,Insecta,between
663,Drosophila melanogaster,46,rayyan-697471387,Spatially varying selection shapes life history clines among populations of Drosophila melanogaster from sub-Saharan Africa,2015,2002-2011,tropical and subtropical sub-Saharan populations,lab,female,female,NA,NA,39,39,NA,NA,NA,NA,230,233,line_mean_correlation,genetic_line,no,broad,CC,adult,both,fecundity 1-5 days (number of egg laid),lifespan of female,fertility,survival,include_2,cor,-0.19,NA,NA,NA,NA,NA,NA,NA,NA,"above-equator (pop EF, ED, CO, EA, NG)",table s6,fertility,survival,genotype,-0.192337169,39,1,-0.192337169,female,cross,Insecta,between
664,Drosophila melanogaster,46,rayyan-697471387,Spatially varying selection shapes life history clines among populations of Drosophila melanogaster from sub-Saharan Africa,2015,2002-2011,tropical and subtropical sub-Saharan populations,lab,female,female,NA,NA,22,22,NA,NA,NA,NA,128,128,line_mean_correlation,genetic_line,no,broad,CC,adult,adult,fecundity 1-5 days (number of egg laid),fecundity 1-10 days (number of eggs laid),fertility,fertility,include_2,cor,0.9,NA,NA,NA,NA,NA,NA,NA,NA,"at-equator (pop RG, GA)",table s6,fertility,fertility,genotype,1.47221949,22,1,1.47221949,female,adult,Insecta,within
665,Drosophila melanogaster,46,rayyan-697471387,Spatially varying selection shapes life history clines among populations of Drosophila melanogaster from sub-Saharan Africa,2015,2002-2011,tropical and subtropical sub-Saharan populations,lab,female,female,NA,NA,22,22,NA,NA,NA,NA,128,130,line_mean_correlation,genetic_line,no,broad,CC,adult,both,fecundity 1-5 days (number of egg laid),lifespan of female,fertility,survival,include_2,cor,-0.23,NA,NA,NA,NA,NA,NA,NA,NA,"at-equator (pop RG, GA)",table s6,fertility,survival,genotype,-0.234189467,22,1,-0.234189467,female,cross,Insecta,between
666,Drosophila melanogaster,46,rayyan-697471387,Spatially varying selection shapes life history clines among populations of Drosophila melanogaster from sub-Saharan Africa,2015,2002-2011,tropical and subtropical sub-Saharan populations,lab,female,both,NA,NA,22,15,NA,NA,NA,NA,128,1050,line_mean_correlation,genetic_line,no,broad,CC,adult,non_adult,fecundity 1-5 days (number of egg laid),proportion egg-to-adult survival (viability),fertility,survival,include_2,cor,-0.63,NA,NA,NA,NA,NA,NA,NA,NA,"at-equator (pop RG, GA)",table s6,fertility,survival,genotype,-0.741416144,15,1,-0.741416144,female,cross,Insecta,between
667,Drosophila melanogaster,46,rayyan-697471387,Spatially varying selection shapes life history clines among populations of Drosophila melanogaster from sub-Saharan Africa,2015,2002-2011,tropical and subtropical sub-Saharan populations,lab,female,female,NA,NA,22,22,NA,NA,NA,NA,128,128,line_mean_correlation,genetic_line,no,broad,CC,adult,adult,fecundity 6-10 days (number of egg laid),fecundity 1-10 days (number of eggs laid),fertility,fertility,include_2,cor,0.91,NA,NA,NA,NA,NA,NA,NA,NA,"at-equator (pop RG, GA)",table s6,fertility,fertility,genotype,1.527524425,22,1,1.527524425,female,adult,Insecta,within
668,Drosophila melanogaster,46,rayyan-697471387,Spatially varying selection shapes life history clines among populations of Drosophila melanogaster from sub-Saharan Africa,2015,2002-2011,tropical and subtropical sub-Saharan populations,lab,female,female,NA,NA,22,22,NA,NA,NA,NA,128,130,line_mean_correlation,genetic_line,no,broad,CC,adult,both,fecundity 6-10 days (number of egg laid),lifespan of female,fertility,survival,include_2,cor,0.16,NA,NA,NA,NA,NA,NA,NA,NA,"at-equator (pop RG, GA)",table s6,fertility,survival,genotype,0.161386696,22,1,0.161386696,female,cross,Insecta,between
669,Drosophila melanogaster,46,rayyan-697471387,Spatially varying selection shapes life history clines among populations of Drosophila melanogaster from sub-Saharan Africa,2015,2002-2011,tropical and subtropical sub-Saharan populations,lab,female,both,NA,NA,22,15,NA,NA,NA,NA,128,1050,line_mean_correlation,genetic_line,no,broad,CC,adult,non_adult,fecundity 6-10 days (number of egg laid),proportion egg-to-adult survival (viability),fertility,survival,include_2,cor,-0.23,NA,NA,NA,NA,NA,NA,NA,NA,"at-equator (pop RG, GA)",table s6,fertility,survival,genotype,-0.234189467,15,1,-0.234189467,female,cross,Insecta,between
670,Drosophila melanogaster,46,rayyan-697471387,Spatially varying selection shapes life history clines among populations of Drosophila melanogaster from sub-Saharan Africa,2015,2002-2011,tropical and subtropical sub-Saharan populations,lab,female,female,NA,NA,22,22,NA,NA,NA,NA,128,130,line_mean_correlation,genetic_line,no,broad,CC,adult,both,fecundity 1-10 days (number of eggs laid),lifespan of female,fertility,survival,include_2,cor,-0.03,NA,NA,NA,NA,NA,NA,NA,NA,"at-equator (pop RG, GA)",table s6,fertility,survival,genotype,-0.030009005,22,1,-0.030009005,female,cross,Insecta,between
671,Drosophila melanogaster,46,rayyan-697471387,Spatially varying selection shapes life history clines among populations of Drosophila melanogaster from sub-Saharan Africa,2015,2002-2011,tropical and subtropical sub-Saharan populations,lab,female,both,NA,NA,22,15,NA,NA,NA,NA,128,1050,line_mean_correlation,genetic_line,no,broad,CC,adult,non_adult,fecundity 1-10 days (number of eggs laid),proportion egg-to-adult survival (viability),fertility,survival,include_2,cor,-0.46,NA,NA,NA,NA,NA,NA,NA,NA,"at-equator (pop RG, GA)",table s6,fertility,survival,genotype,-0.497311288,15,1,-0.497311288,female,cross,Insecta,between
675,Drosophila melanogaster,46,rayyan-697471387,Spatially varying selection shapes life history clines among populations of Drosophila melanogaster from sub-Saharan Africa,2015,2002-2011,tropical and subtropical sub-Saharan populations,lab,female,female,NA,NA,26,26,NA,NA,NA,NA,286,145,line_mean_correlation,genetic_line,no,broad,CC,adult,adult,thorax length of 1 to 3 day odd adult females,fecundity 1-10 days (number of eggs laid),size,fertility,include_2,cor,0.2,NA,NA,NA,NA,NA,NA,NA,NA,"below-equator (pop SF, SP, SE)",table s6,size,fertility,genotype,0.202732554,26,1,0.202732554,female,adult,Insecta,between
676,Drosophila melanogaster,46,rayyan-697471387,Spatially varying selection shapes life history clines among populations of Drosophila melanogaster from sub-Saharan Africa,2015,2002-2011,tropical and subtropical sub-Saharan populations,lab,female,female,NA,NA,26,26,NA,NA,NA,NA,286,177,line_mean_correlation,genetic_line,no,broad,CC,adult,both,thorax length of 1 to 3 day odd adult females,lifespan of female,size,survival,include_2,cor,-0.25,NA,NA,NA,NA,NA,NA,NA,NA,"below-equator (pop SF, SP, SE)",table s6,size,survival,genotype,-0.255412812,26,1,-0.255412812,female,cross,Insecta,between
677,Drosophila melanogaster,46,rayyan-697471387,Spatially varying selection shapes life history clines among populations of Drosophila melanogaster from sub-Saharan Africa,2015,2002-2011,tropical and subtropical sub-Saharan populations,lab,female,both,NA,NA,26,26,NA,NA,NA,NA,286,1650,line_mean_correlation,genetic_line,no,broad,CC,adult,non_adult,thorax length of 1 to 3 day odd adult females,proportion egg-to-adult survival (viability),size,survival,include_2,cor,0.26,NA,NA,NA,NA,NA,NA,NA,NA,"below-equator (pop SF, SP, SE)",table s6,size,survival,genotype,0.266108407,26,1,0.266108407,female,cross,Insecta,between
678,Drosophila melanogaster,46,rayyan-697471387,Spatially varying selection shapes life history clines among populations of Drosophila melanogaster from sub-Saharan Africa,2015,2002-2011,tropical and subtropical sub-Saharan populations,lab,female,female,NA,NA,26,26,NA,NA,NA,NA,176,145,line_mean_correlation,genetic_line,no,broad,CC,adult,adult,fecundity 1-5 days (number of egg laid),fecundity 6-10 days (number of egg laid),fertility,fertility,include_2,cor,0.68,NA,NA,NA,NA,NA,NA,NA,NA,"below-equator (pop SF, SP, SE)",table s6,fertility,fertility,genotype,0.829114038,26,1,0.829114038,female,adult,Insecta,within
679,Drosophila melanogaster,46,rayyan-697471387,Spatially varying selection shapes life history clines among populations of Drosophila melanogaster from sub-Saharan Africa,2015,2002-2011,tropical and subtropical sub-Saharan populations,lab,female,female,NA,NA,26,26,NA,NA,NA,NA,176,145,line_mean_correlation,genetic_line,no,broad,CC,adult,adult,fecundity 1-5 days (number of egg laid),fecundity 1-10 days (number of eggs laid),fertility,fertility,include_2,cor,0.87,NA,NA,NA,NA,NA,NA,NA,NA,"below-equator (pop SF, SP, SE)",table s6,fertility,fertility,genotype,1.33307963,26,1,1.33307963,female,adult,Insecta,within
680,Drosophila melanogaster,46,rayyan-697471387,Spatially varying selection shapes life history clines among populations of Drosophila melanogaster from sub-Saharan Africa,2015,2002-2011,tropical and subtropical sub-Saharan populations,lab,female,female,NA,NA,26,26,NA,NA,NA,NA,176,177,line_mean_correlation,genetic_line,no,broad,CC,adult,both,fecundity 1-5 days (number of egg laid),lifespan of female,fertility,survival,include_2,cor,-0.37,NA,NA,NA,NA,NA,NA,NA,NA,"below-equator (pop SF, SP, SE)",table s6,fertility,survival,genotype,-0.3884231,26,1,-0.3884231,female,cross,Insecta,between
681,Drosophila melanogaster,46,rayyan-697471387,Spatially varying selection shapes life history clines among populations of Drosophila melanogaster from sub-Saharan Africa,2015,2002-2011,tropical and subtropical sub-Saharan populations,lab,female,both,NA,NA,26,26,NA,NA,NA,NA,176,1650,line_mean_correlation,genetic_line,no,broad,CC,adult,non_adult,fecundity 1-5 days (number of egg laid),proportion egg-to-adult survival (viability),fertility,survival,include_2,cor,0.14,NA,NA,NA,NA,NA,NA,NA,NA,"below-equator (pop SF, SP, SE)",table s6,fertility,survival,genotype,0.140925576,26,1,0.140925576,female,cross,Insecta,between
682,Drosophila melanogaster,46,rayyan-697471387,Spatially varying selection shapes life history clines among populations of Drosophila melanogaster from sub-Saharan Africa,2015,2002-2011,tropical and subtropical sub-Saharan populations,lab,female,female,NA,NA,26,26,NA,NA,NA,NA,145,145,line_mean_correlation,genetic_line,no,broad,CC,adult,adult,fecundity 6-10 days (number of egg laid),fecundity 1-10 days (number of eggs laid),fertility,fertility,include_2,cor,0.94,NA,NA,NA,NA,NA,NA,NA,NA,"below-equator (pop SF, SP, SE)",table s6,fertility,fertility,genotype,1.738049345,26,1,1.738049345,female,adult,Insecta,within
683,Drosophila melanogaster,46,rayyan-697471387,Spatially varying selection shapes life history clines among populations of Drosophila melanogaster from sub-Saharan Africa,2015,2002-2011,tropical and subtropical sub-Saharan populations,lab,female,female,NA,NA,26,26,NA,NA,NA,NA,145,177,line_mean_correlation,genetic_line,no,broad,CC,adult,both,fecundity 6-10 days (number of egg laid),lifespan of female,fertility,survival,include_2,cor,-0.08,NA,NA,NA,NA,NA,NA,NA,NA,"below-equator (pop SF, SP, SE)",table s6,fertility,survival,genotype,-0.080171325,26,1,-0.080171325,female,cross,Insecta,between
684,Drosophila melanogaster,46,rayyan-697471387,Spatially varying selection shapes life history clines among populations of Drosophila melanogaster from sub-Saharan Africa,2015,2002-2011,tropical and subtropical sub-Saharan populations,lab,female,both,NA,NA,26,26,NA,NA,NA,NA,145,1650,line_mean_correlation,genetic_line,no,broad,CC,adult,non_adult,fecundity 6-10 days (number of egg laid),proportion egg-to-adult survival (viability),fertility,survival,include_2,cor,0.01,NA,NA,NA,NA,NA,NA,NA,NA,"below-equator (pop SF, SP, SE)",table s6,fertility,survival,genotype,0.010000333,26,1,0.010000333,female,cross,Insecta,between
685,Drosophila melanogaster,46,rayyan-697471387,Spatially varying selection shapes life history clines among populations of Drosophila melanogaster from sub-Saharan Africa,2015,2002-2011,tropical and subtropical sub-Saharan populations,lab,female,female,NA,NA,26,26,NA,NA,NA,NA,145,177,line_mean_correlation,genetic_line,no,broad,CC,adult,both,fecundity 1-10 days (number of eggs laid),lifespan of female,fertility,survival,include_2,cor,-0.26,NA,NA,NA,NA,NA,NA,NA,NA,"below-equator (pop SF, SP, SE)",table s6,fertility,survival,genotype,-0.266108407,26,1,-0.266108407,female,cross,Insecta,between
686,Drosophila melanogaster,46,rayyan-697471387,Spatially varying selection shapes life history clines among populations of Drosophila melanogaster from sub-Saharan Africa,2015,2002-2011,tropical and subtropical sub-Saharan populations,lab,female,both,NA,NA,26,26,NA,NA,NA,NA,145,1650,line_mean_correlation,genetic_line,no,broad,CC,adult,non_adult,fecundity 1-10 days (number of eggs laid),proportion egg-to-adult survival (viability),fertility,survival,include_2,cor,0.04,NA,NA,NA,NA,NA,NA,NA,NA,"below-equator (pop SF, SP, SE)",table s6,fertility,survival,genotype,0.040021354,26,1,0.040021354,female,cross,Insecta,between
687,Drosophila melanogaster,46,rayyan-697471387,Spatially varying selection shapes life history clines among populations of Drosophila melanogaster from sub-Saharan Africa,2015,2002-2011,tropical and subtropical sub-Saharan populations,lab,female,both,NA,NA,26,26,NA,NA,NA,NA,177,1650,line_mean_correlation,genetic_line,no,broad,CC,both,non_adult,lifespan of female,proportion egg-to-adult survival (viability),survival,survival,include_2,cor,0.2,NA,NA,NA,NA,NA,NA,NA,NA,"below-equator (pop SF, SP, SE)",table s6,survival,survival,genotype,0.202732554,26,1,0.202732554,female,cross,Insecta,within
697,Drosophila melanogaster,46,rayyan-697471387,Spatially varying selection shapes life history clines among populations of Drosophila melanogaster from sub-Saharan Africa,2015,2002-2011,tropical and subtropical sub-Saharan populations,lab,female,both,NA,NA,39,38,NA,NA,NA,NA,233,2265,line_mean_correlation,genetic_line,no,broad,CC,both,non_adult,lifespan of female,proportion egg-to-adult survival (viability),survival,survival,include_2,cor,-0.12,NA,NA,NA,NA,NA,NA,NA,NA,"above-equator (pop EF, ED, CO, EA, NG)",table s6,survival,survival,genotype,-0.120581028,38,1,-0.120581028,female,cross,Insecta,within
703,Drosophila melanogaster,46,rayyan-697471387,Spatially varying selection shapes life history clines among populations of Drosophila melanogaster from sub-Saharan Africa,2015,2002-2011,tropical and subtropical sub-Saharan populations,lab,female,female,NA,NA,22,22,NA,NA,NA,NA,128,128,line_mean_correlation,genetic_line,no,broad,CC,adult,adult,fecundity 1-5 days (number of egg laid),fecundity 6-10 days (number of egg laid),fertility,fertility,include_2,cor,0.65,NA,NA,NA,NA,NA,NA,NA,NA,"at-equator (pop RG, GA)",table s6,fertility,fertility,genotype,0.775298706,22,1,0.775298706,female,adult,Insecta,within
718,Drosophila melanogaster,56,rayyan-697471482,Pleiotropy and life history evolution in drosophila melanogaster: Uncoupling life span and early fecundity,2013,NA,NA,lab,female,female,NA,NA,57,57,NA,NA,NA,NA,7980,NA,line_mean_correlation,genetic_line,no,broad,CC,both,adult,mean female lifespan,number of eggs laid on day 1/number of live females,survival,fertility,include,cor,0.041394336,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-697471482,figure 8,survival,fertility,genotype,0.041418003,57,1,0.041418003,female,cross,Insecta,between
719,Drosophila melanogaster,56,rayyan-697471482,Pleiotropy and life history evolution in drosophila melanogaster: Uncoupling life span and early fecundity,2013,NA,NA,lab,female,female,NA,NA,57,57,NA,NA,NA,NA,7980,NA,line_mean_correlation,genetic_line,no,broad,CC,both,adult,mean female lifespan,number of eggs laid on day 4/number of live females,survival,fertility,include,cor,-0.181917211,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-697471482,figure 8,survival,fertility,genotype,-0.183964807,57,1,-0.183964807,female,cross,Insecta,between
720,Drosophila melanogaster,56,rayyan-697471482,Pleiotropy and life history evolution in drosophila melanogaster: Uncoupling life span and early fecundity,2013,NA,NA,lab,female,female,NA,NA,57,57,NA,NA,NA,NA,7980,NA,line_mean_correlation,genetic_line,no,broad,CC,both,adult,mean female lifespan,number of eggs laid on day 7/number of live females,survival,fertility,include,cor,0.000544662,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-697471482,figure 8,survival,fertility,genotype,0.000544662,57,1,0.000544662,female,cross,Insecta,between
721,Drosophila melanogaster,56,rayyan-697471482,Pleiotropy and life history evolution in drosophila melanogaster: Uncoupling life span and early fecundity,2013,NA,NA,lab,female,female,NA,NA,57,57,NA,NA,NA,NA,7980,NA,line_mean_correlation,genetic_line,no,broad,CC,both,adult,mean female lifespan,number of eggs laid on day 10/number of live females,survival,fertility,include,cor,-0.206427015,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-697471482,figure 8,survival,fertility,genotype,-0.209436438,57,1,-0.209436438,female,cross,Insecta,between
722,Drosophila melanogaster,56,rayyan-697471482,Pleiotropy and life history evolution in drosophila melanogaster: Uncoupling life span and early fecundity,2013,NA,NA,lab,female,female,NA,NA,57,57,NA,NA,NA,NA,7980,NA,line_mean_correlation,genetic_line,no,broad,CC,both,adult,mean female lifespan,number of eggs laid on day 13/number of live females,survival,fertility,include,cor,0.022331155,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-697471482,figure 8,survival,fertility,genotype,0.022334868,57,1,0.022334868,female,cross,Insecta,between
723,Drosophila melanogaster,56,rayyan-697471482,Pleiotropy and life history evolution in drosophila melanogaster: Uncoupling life span and early fecundity,2013,NA,NA,lab,female,female,NA,NA,57,57,NA,NA,NA,NA,7980,NA,line_mean_correlation,genetic_line,no,broad,CC,both,adult,mean female lifespan,number of eggs laid on day 16/number of live females,survival,fertility,include,cor,0.005991285,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-697471482,figure 8,survival,fertility,genotype,0.005991357,57,1,0.005991357,female,cross,Insecta,between
724,Drosophila melanogaster,56,rayyan-697471482,Pleiotropy and life history evolution in drosophila melanogaster: Uncoupling life span and early fecundity,2013,NA,NA,lab,female,female,NA,NA,57,57,NA,NA,NA,NA,7980,NA,line_mean_correlation,genetic_line,no,broad,CC,both,adult,mean female lifespan,number of eggs laid on day 19/number of live females,survival,fertility,include,cor,-0.173747277,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-697471482,figure 8,survival,fertility,genotype,-0.175528012,57,1,-0.175528012,female,cross,Insecta,between
725,Drosophila melanogaster,56,rayyan-697471482,Pleiotropy and life history evolution in drosophila melanogaster: Uncoupling life span and early fecundity,2013,NA,NA,lab,female,female,NA,NA,57,57,NA,NA,NA,NA,7980,NA,line_mean_correlation,genetic_line,no,broad,CC,both,adult,mean female lifespan,number of eggs laid on day 22/number of live females,survival,fertility,include,cor,-0.048474946,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-697471482,figure 8,survival,fertility,genotype,-0.048512969,57,1,-0.048512969,female,cross,Insecta,between
726,Drosophila melanogaster,56,rayyan-697471482,Pleiotropy and life history evolution in drosophila melanogaster: Uncoupling life span and early fecundity,2013,NA,NA,lab,female,female,NA,NA,57,57,NA,NA,NA,NA,7980,NA,line_mean_correlation,genetic_line,no,broad,CC,both,adult,mean female lifespan,number of eggs laid on day 25/number of live females,survival,fertility,include,cor,0.169389978,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-697471482,figure 8,survival,fertility,genotype,0.171038554,57,1,0.171038554,female,cross,Insecta,between
727,Drosophila melanogaster,56,rayyan-697471482,Pleiotropy and life history evolution in drosophila melanogaster: Uncoupling life span and early fecundity,2013,NA,NA,lab,female,female,NA,NA,57,57,NA,NA,NA,NA,7980,NA,line_mean_correlation,genetic_line,no,broad,CC,both,adult,mean female lifespan,number of eggs laid on day 28/number of live females,survival,fertility,include,cor,0.294662309,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-697471482,figure 8,survival,fertility,genotype,0.303664246,57,1,0.303664246,female,cross,Insecta,between
728,Drosophila melanogaster,56,rayyan-697471482,Pleiotropy and life history evolution in drosophila melanogaster: Uncoupling life span and early fecundity,2013,NA,NA,lab,female,female,NA,NA,57,57,NA,NA,NA,NA,7980,NA,line_mean_correlation,genetic_line,no,broad,CC,both,adult,mean female lifespan,number of eggs laid on day 31/number of live females,survival,fertility,include,cor,0.618736383,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-697471482,figure 8,survival,fertility,genotype,0.722955035,57,1,0.722955035,female,cross,Insecta,between
729,Drosophila melanogaster,56,rayyan-697471482,Pleiotropy and life history evolution in drosophila melanogaster: Uncoupling life span and early fecundity,2013,NA,NA,lab,female,female,NA,NA,57,57,NA,NA,NA,NA,7980,NA,line_mean_correlation,genetic_line,no,broad,CC,both,adult,mean female lifespan,number of eggs laid on day 34/number of live females,survival,fertility,include,cor,0.616013072,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-697471482,figure 8,survival,fertility,genotype,0.718554409,57,1,0.718554409,female,cross,Insecta,between
730,Drosophila melanogaster,56,rayyan-697471482,Pleiotropy and life history evolution in drosophila melanogaster: Uncoupling life span and early fecundity,2013,NA,NA,lab,female,female,NA,NA,57,57,NA,NA,NA,NA,7980,NA,line_mean_correlation,genetic_line,no,broad,CC,both,adult,mean female lifespan,number of eggs laid on day 37/number of live females,survival,fertility,include,cor,0.632352941,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-697471482,figure 8,survival,fertility,genotype,0.745327188,57,1,0.745327188,female,cross,Insecta,between
731,Drosophila melanogaster,56,rayyan-697471482,Pleiotropy and life history evolution in drosophila melanogaster: Uncoupling life span and early fecundity,2013,NA,NA,lab,female,female,NA,NA,57,57,NA,NA,NA,NA,7980,NA,line_mean_correlation,genetic_line,no,broad,CC,both,adult,mean female lifespan,number of eggs laid on day 40/number of live females,survival,fertility,include,cor,0.61328976,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-697471482,figure 8,survival,fertility,genotype,0.714177512,57,1,0.714177512,female,cross,Insecta,between
732,Drosophila melanogaster,56,rayyan-697471482,Pleiotropy and life history evolution in drosophila melanogaster: Uncoupling life span and early fecundity,2013,NA,NA,lab,female,female,NA,NA,57,57,NA,NA,NA,NA,7980,NA,line_mean_correlation,genetic_line,no,broad,CC,both,adult,mean female lifespan,number of eggs laid on day 43/number of live females,survival,fertility,include,cor,0.714052288,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-697471482,figure 8,survival,fertility,genotype,0.895403318,57,1,0.895403318,female,cross,Insecta,between
733,Drosophila melanogaster,56,rayyan-697471482,Pleiotropy and life history evolution in drosophila melanogaster: Uncoupling life span and early fecundity,2013,NA,NA,lab,female,female,NA,NA,57,57,NA,NA,NA,NA,7980,NA,line_mean_correlation,genetic_line,no,broad,CC,both,adult,mean female lifespan,number of eggs laid on day 46/number of live females,survival,fertility,include,cor,0.558823529,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-697471482,figure 8,survival,fertility,genotype,0.631120856,57,1,0.631120856,female,cross,Insecta,between
734,Drosophila melanogaster,56,rayyan-697471482,Pleiotropy and life history evolution in drosophila melanogaster: Uncoupling life span and early fecundity,2013,NA,NA,lab,female,female,NA,NA,57,57,NA,NA,NA,NA,7980,NA,line_mean_correlation,genetic_line,no,broad,CC,both,adult,mean female lifespan,number of eggs laid on day 49/number of live females,survival,fertility,include,cor,0.528867102,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-697471482,figure 8,survival,fertility,genotype,0.588571034,57,1,0.588571034,female,cross,Insecta,between
735,Drosophila melanogaster,56,rayyan-697471482,Pleiotropy and life history evolution in drosophila melanogaster: Uncoupling life span and early fecundity,2013,NA,NA,lab,female,female,NA,NA,57,57,NA,NA,NA,NA,7980,NA,line_mean_correlation,genetic_line,no,broad,CC,both,adult,mean female lifespan,number of eggs laid on day 52/number of live females,survival,fertility,include,cor,0.452614379,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-697471482,figure 8,survival,fertility,genotype,0.487983352,57,1,0.487983352,female,cross,Insecta,between
736,Drosophila melanogaster,56,rayyan-697471482,Pleiotropy and life history evolution in drosophila melanogaster: Uncoupling life span and early fecundity,2013,NA,NA,lab,female,female,NA,NA,57,57,NA,NA,NA,NA,7980,NA,line_mean_correlation,genetic_line,no,broad,CC,both,adult,mean female lifespan,number of eggs laid on day 55/number of live females,survival,fertility,include,cor,0.561546841,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-697471482,figure 8,survival,fertility,genotype,0.635089594,57,1,0.635089594,female,cross,Insecta,between
737,Drosophila melanogaster,56,rayyan-697471482,Pleiotropy and life history evolution in drosophila melanogaster: Uncoupling life span and early fecundity,2013,NA,NA,lab,female,female,NA,NA,57,57,NA,NA,NA,NA,7980,NA,line_mean_correlation,genetic_line,no,broad,CC,both,adult,mean female lifespan,number of eggs laid on day 58/number of live females,survival,fertility,include,cor,0.550653595,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-697471482,figure 8,survival,fertility,genotype,0.619318851,57,1,0.619318851,female,cross,Insecta,between
738,Drosophila melanogaster,125,rayyan-697471866,Effects on fitness components of P-element inserts in Drosophila melanogaster: Analysis of trade-offs,1996,NA,NA,lab,both,both,NA,NA,12,12,NA,NA,NA,NA,720,7200,line_mean_correlation,genetic_line,no,broad,CC,adult,both,birth rate in the first five days after eclosion,mortality in the 10-15 days,fertility,reverse_survival,include,cor,0.602094241,NA,NA,NA,NA,NA,NA,NA,NA,29,figure 5b,fertility,survival,genotype,0.696425881,12,-1,-0.696425881,both,cross,Insecta,between
747,Drosophila melanogaster,422,rayyan-697473383,The evolutionary costs of immunological maintenance and deployment,2008,2004,"Newfield, NY, USA",lab,female,female,NA,NA,40,40,NA,NA,NA,NA,NA,NA,line_mean_correlation,genetic_line,no,broad,CC,adult,adult,fecundity,weight gain (day 9 weight minus emergence weight),fertility,growth,include,cor,0.409,NA,NA,NA,NA,NA,NA,NA,NA,unlimited,table 3,fertility,growth,genotype,0.434409747,40,1,0.434409747,female,adult,Insecta,between
748,Drosophila melanogaster,258,rayyan-197247442,Spontaneous mutation for life-history traits in Drosophila melanogaster,1998,NA,NA,lab,female,female,NA,NA,6,6,NA,NA,NA,NA,NA,NA,line_mean_correlation,genetic_line,no,broad,authors,adult,non_adult,early fecundity (number of eggs),early viability (percentage of eggs developing into pupae),fertility,survival,include,cor,0.55,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-197247442,table 6,fertility,survival,genotype,0.618381314,6,1,0.618381314,female,cross,Insecta,between
749,Drosophila melanogaster,258,rayyan-197247442,Spontaneous mutation for life-history traits in Drosophila melanogaster,1998,NA,NA,lab,female,female,NA,NA,6,6,NA,NA,NA,NA,NA,NA,line_mean_correlation,genetic_line,no,broad,authors,adult,adult,early fecundity (number of eggs),early pupal productivity (number of pupae produced),fertility,fertility,include,cor,0.83,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-197247442,table 6,fertility,fertility,genotype,1.188136404,6,1,1.188136404,female,adult,Insecta,within
751,Drosophila melanogaster,258,rayyan-197247442,Spontaneous mutation for life-history traits in Drosophila melanogaster,1998,NA,NA,lab,female,female,NA,NA,6,6,NA,NA,NA,NA,NA,NA,line_mean_correlation,genetic_line,no,broad,authors,adult,adult,early fecundity (number of eggs),late fecundity (number of eggs),fertility,fertility,include,cor,0.56,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-197247442,table 6,fertility,fertility,genotype,0.632833187,6,1,0.632833187,female,adult,Insecta,within
752,Drosophila melanogaster,258,rayyan-197247442,Spontaneous mutation for life-history traits in Drosophila melanogaster,1998,NA,NA,lab,female,female,NA,NA,6,6,NA,NA,NA,NA,NA,NA,line_mean_correlation,genetic_line,no,broad,authors,adult,non_adult,early fecundity (number of eggs),late viability (percentage of eggs developing into pupae),fertility,survival,include,cor,0.6,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-197247442,table 6,fertility,survival,genotype,0.693147181,6,1,0.693147181,female,cross,Insecta,between
753,Drosophila melanogaster,258,rayyan-197247442,Spontaneous mutation for life-history traits in Drosophila melanogaster,1998,NA,NA,lab,female,female,NA,NA,6,6,NA,NA,NA,NA,NA,NA,line_mean_correlation,genetic_line,no,broad,authors,adult,adult,early fecundity (number of eggs),late pupal productivity (number of pupae produced),fertility,fertility,include,cor,0.69,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-197247442,table 6,fertility,fertility,genotype,0.847955755,6,1,0.847955755,female,adult,Insecta,within
754,Drosophila melanogaster,258,rayyan-197247442,Spontaneous mutation for life-history traits in Drosophila melanogaster,1998,NA,NA,lab,female,female,NA,NA,6,6,NA,NA,NA,NA,NA,NA,line_mean_correlation,genetic_line,no,broad,authors,non_adult,adult,early viability  (percentage of eggs developing into pupae),early pupal productivity (number of pupae produced),survival,fertility,include,cor,0.92,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-197247442,table 6,survival,fertility,genotype,1.589026915,6,1,1.589026915,female,cross,Insecta,between
755,Drosophila melanogaster,368,rayyan-697472840,"Life history variation in an artificially selected population of drosophila melanogaster: Pleiotropy, superflies, and age-specific adaptation",2010,NA,NA,lab,female,female,NA,NA,58,58,NA,NA,NA,NA,13200,13200,line_mean_correlation,genetic_line,yes,broad,authors,both,adult,lifespan,early fecundity,survival,fertility,include,cor,0.09,NA,NA,NA,NA,NA,NA,NA,NA,female_raw_all,table 1,survival,fertility,genotype,0.090244188,58,1,0.090244188,female,cross,Insecta,between
756,Drosophila melanogaster,368,rayyan-697472840,"Life history variation in an artificially selected population of drosophila melanogaster: Pleiotropy, superflies, and age-specific adaptation",2010,NA,NA,lab,female,female,NA,NA,58,58,NA,NA,NA,NA,13200,13200,line_mean_correlation,genetic_line,yes,broad,authors,both,adult,lifespan,midlife fecundity,survival,fertility,include,cor,0.55,NA,NA,NA,NA,NA,NA,NA,NA,female_raw_all,table 1,survival,fertility,genotype,0.618381314,58,1,0.618381314,female,cross,Insecta,between
757,Drosophila melanogaster,368,rayyan-697472840,"Life history variation in an artificially selected population of drosophila melanogaster: Pleiotropy, superflies, and age-specific adaptation",2010,NA,NA,lab,female,female,NA,NA,58,58,NA,NA,NA,NA,13200,13200,line_mean_correlation,genetic_line,yes,broad,authors,both,adult,lifespan,total fecundity,survival,fertility,include,cor,0.49,NA,NA,NA,NA,NA,NA,NA,NA,female_raw_all,table 1,survival,fertility,genotype,0.536060337,58,1,0.536060337,female,cross,Insecta,between
758,Drosophila melanogaster,368,rayyan-697472840,"Life history variation in an artificially selected population of drosophila melanogaster: Pleiotropy, superflies, and age-specific adaptation",2010,NA,NA,lab,male,male,NA,NA,58,58,NA,NA,NA,NA,13200,13200,line_mean_correlation,genetic_line,yes,broad,authors,both,adult,lifespan,early fecundity,survival,fertility,include,cor,0.08,NA,NA,NA,NA,NA,NA,NA,NA,male_raw_all,table 1,survival,fertility,genotype,0.080171325,58,1,0.080171325,male,cross,Insecta,between
759,Drosophila melanogaster,368,rayyan-697472840,"Life history variation in an artificially selected population of drosophila melanogaster: Pleiotropy, superflies, and age-specific adaptation",2010,NA,NA,lab,male,male,NA,NA,58,58,NA,NA,NA,NA,13200,13200,line_mean_correlation,genetic_line,yes,broad,authors,both,adult,lifespan,midlife fecundity,survival,fertility,include,cor,0.71,NA,NA,NA,NA,NA,NA,NA,NA,male_raw_all,table 1,survival,fertility,genotype,0.887183863,58,1,0.887183863,male,cross,Insecta,between
760,Drosophila melanogaster,368,rayyan-697472840,"Life history variation in an artificially selected population of drosophila melanogaster: Pleiotropy, superflies, and age-specific adaptation",2010,NA,NA,lab,male,male,NA,NA,58,58,NA,NA,NA,NA,13200,13200,line_mean_correlation,genetic_line,yes,broad,authors,both,adult,lifespan,total fecundity,survival,fertility,include,cor,0.63,NA,NA,NA,NA,NA,NA,NA,NA,male_raw_all,table 1,survival,fertility,genotype,0.741416144,58,1,0.741416144,male,cross,Insecta,between
779,Drosophila melanogaster,368,rayyan-697472840,"Life history variation in an artificially selected population of drosophila melanogaster: Pleiotropy, superflies, and age-specific adaptation",2010,NA,NA,lab,female,female,NA,NA,58,58,NA,NA,NA,NA,NA,NA,line_mean_correlation,genetic_line,yes,broad,authors,both,adult,female lifespan,daily fecundity,survival,fertility,include,cor,0.189,NA,NA,NA,NA,NA,NA,NA,NA,female_raw_all_daily_1,figure 5,survival,fertility,genotype,0.191299921,58,1,0.191299921,female,cross,Insecta,between
780,Drosophila melanogaster,368,rayyan-697472840,"Life history variation in an artificially selected population of drosophila melanogaster: Pleiotropy, superflies, and age-specific adaptation",2010,NA,NA,lab,female,female,NA,NA,58,58,NA,NA,NA,NA,NA,NA,line_mean_correlation,genetic_line,yes,broad,authors,both,adult,female lifespan,daily fecundity,survival,fertility,include,cor,-0.162,NA,NA,NA,NA,NA,NA,NA,NA,female_raw_all_daily_2,figure 5,survival,fertility,genotype,-0.163439918,58,1,-0.163439918,female,cross,Insecta,between
781,Drosophila melanogaster,368,rayyan-697472840,"Life history variation in an artificially selected population of drosophila melanogaster: Pleiotropy, superflies, and age-specific adaptation",2010,NA,NA,lab,female,female,NA,NA,58,58,NA,NA,NA,NA,NA,NA,line_mean_correlation,genetic_line,yes,broad,authors,both,adult,female lifespan,daily fecundity,survival,fertility,include,cor,0.258,NA,NA,NA,NA,NA,NA,NA,NA,female_raw_all_daily_3,figure 5,survival,fertility,genotype,0.263964597,58,1,0.263964597,female,cross,Insecta,between
782,Drosophila melanogaster,368,rayyan-697472840,"Life history variation in an artificially selected population of drosophila melanogaster: Pleiotropy, superflies, and age-specific adaptation",2010,NA,NA,lab,female,female,NA,NA,58,58,NA,NA,NA,NA,NA,NA,line_mean_correlation,genetic_line,yes,broad,authors,both,adult,female lifespan,daily fecundity,survival,fertility,include,cor,0.141,NA,NA,NA,NA,NA,NA,NA,NA,female_raw_all_daily_4,figure 5,survival,fertility,genotype,0.141945714,58,1,0.141945714,female,cross,Insecta,between
783,Drosophila melanogaster,368,rayyan-697472840,"Life history variation in an artificially selected population of drosophila melanogaster: Pleiotropy, superflies, and age-specific adaptation",2010,NA,NA,lab,female,female,NA,NA,58,58,NA,NA,NA,NA,NA,NA,line_mean_correlation,genetic_line,yes,broad,authors,both,adult,female lifespan,daily fecundity,survival,fertility,include,cor,0.37,NA,NA,NA,NA,NA,NA,NA,NA,female_raw_all_daily_5,figure 5,survival,fertility,genotype,0.3884231,58,1,0.3884231,female,cross,Insecta,between
784,Drosophila melanogaster,368,rayyan-697472840,"Life history variation in an artificially selected population of drosophila melanogaster: Pleiotropy, superflies, and age-specific adaptation",2010,NA,NA,lab,female,female,NA,NA,58,58,NA,NA,NA,NA,NA,NA,line_mean_correlation,genetic_line,yes,broad,authors,both,adult,female lifespan,daily fecundity,survival,fertility,include,cor,0.257,NA,NA,NA,NA,NA,NA,NA,NA,female_raw_all_daily_6,figure 5,survival,fertility,genotype,0.262893582,58,1,0.262893582,female,cross,Insecta,between
785,Drosophila melanogaster,368,rayyan-697472840,"Life history variation in an artificially selected population of drosophila melanogaster: Pleiotropy, superflies, and age-specific adaptation",2010,NA,NA,lab,female,female,NA,NA,58,58,NA,NA,NA,NA,NA,NA,line_mean_correlation,genetic_line,yes,broad,authors,both,adult,female lifespan,daily fecundity,survival,fertility,include,cor,0.301,NA,NA,NA,NA,NA,NA,NA,NA,female_raw_all_daily_7,figure 5,survival,fertility,genotype,0.310618868,58,1,0.310618868,female,cross,Insecta,between
786,Drosophila melanogaster,368,rayyan-697472840,"Life history variation in an artificially selected population of drosophila melanogaster: Pleiotropy, superflies, and age-specific adaptation",2010,NA,NA,lab,female,female,NA,NA,58,58,NA,NA,NA,NA,NA,NA,line_mean_correlation,genetic_line,yes,broad,authors,both,adult,female lifespan,daily fecundity,survival,fertility,include,cor,0.312,NA,NA,NA,NA,NA,NA,NA,NA,female_raw_all_daily_8,figure 5,survival,fertility,genotype,0.322759566,58,1,0.322759566,female,cross,Insecta,between
787,Drosophila melanogaster,368,rayyan-697472840,"Life history variation in an artificially selected population of drosophila melanogaster: Pleiotropy, superflies, and age-specific adaptation",2010,NA,NA,lab,female,female,NA,NA,58,58,NA,NA,NA,NA,NA,NA,line_mean_correlation,genetic_line,yes,broad,authors,both,adult,female lifespan,daily fecundity,survival,fertility,include,cor,0.611,NA,NA,NA,NA,NA,NA,NA,NA,female_raw_all_daily_9,figure 5,survival,fertility,genotype,0.71051552,58,1,0.71051552,female,cross,Insecta,between
788,Drosophila melanogaster,368,rayyan-697472840,"Life history variation in an artificially selected population of drosophila melanogaster: Pleiotropy, superflies, and age-specific adaptation",2010,NA,NA,lab,female,female,NA,NA,58,58,NA,NA,NA,NA,NA,NA,line_mean_correlation,genetic_line,yes,broad,authors,both,adult,female lifespan,daily fecundity,survival,fertility,include,cor,0.512,NA,NA,NA,NA,NA,NA,NA,NA,female_raw_all_daily_10,figure 5,survival,fertility,genotype,0.565436575,58,1,0.565436575,female,cross,Insecta,between
789,Drosophila melanogaster,368,rayyan-697472840,"Life history variation in an artificially selected population of drosophila melanogaster: Pleiotropy, superflies, and age-specific adaptation",2010,NA,NA,lab,female,female,NA,NA,58,58,NA,NA,NA,NA,NA,NA,line_mean_correlation,genetic_line,yes,broad,authors,both,adult,female lifespan,daily fecundity,survival,fertility,include,cor,0.439,NA,NA,NA,NA,NA,NA,NA,NA,female_raw_all_daily_11,figure 5,survival,fertility,genotype,0.470991401,58,1,0.470991401,female,cross,Insecta,between
790,Drosophila melanogaster,368,rayyan-697472840,"Life history variation in an artificially selected population of drosophila melanogaster: Pleiotropy, superflies, and age-specific adaptation",2010,NA,NA,lab,female,female,NA,NA,58,58,NA,NA,NA,NA,NA,NA,line_mean_correlation,genetic_line,yes,broad,authors,both,adult,female lifespan,daily fecundity,survival,fertility,include,cor,0.447,NA,NA,NA,NA,NA,NA,NA,NA,female_raw_all_daily_12,figure 5,survival,fertility,genotype,0.480944863,58,1,0.480944863,female,cross,Insecta,between
791,Drosophila melanogaster,368,rayyan-697472840,"Life history variation in an artificially selected population of drosophila melanogaster: Pleiotropy, superflies, and age-specific adaptation",2010,NA,NA,lab,female,female,NA,NA,58,58,NA,NA,NA,NA,NA,NA,line_mean_correlation,genetic_line,yes,broad,authors,both,adult,female lifespan,daily fecundity,survival,fertility,include,cor,0.326,NA,NA,NA,NA,NA,NA,NA,NA,female_raw_all_daily_13,figure 5,survival,fertility,genotype,0.33834603,58,1,0.33834603,female,cross,Insecta,between
792,Drosophila melanogaster,368,rayyan-697472840,"Life history variation in an artificially selected population of drosophila melanogaster: Pleiotropy, superflies, and age-specific adaptation",2010,NA,NA,lab,female,female,NA,NA,58,58,NA,NA,NA,NA,NA,NA,line_mean_correlation,genetic_line,yes,broad,authors,both,adult,female lifespan,daily fecundity,survival,fertility,include,cor,0.542,NA,NA,NA,NA,NA,NA,NA,NA,female_raw_all_daily_14,figure 5,survival,fertility,genotype,0.606983185,58,1,0.606983185,female,cross,Insecta,between
793,Drosophila melanogaster,46,rayyan-697471387,Spatially varying selection shapes life history clines among populations of Drosophila melanogaster from sub-Saharan Africa,2015,2002-2011,tropical and subtropical sub-Saharan populations,lab,female,both,NA,NA,22,15,NA,NA,NA,NA,130,1050,line_mean_correlation,genetic_line,no,broad,CC,both,non_adult,lifespan of female,proportion egg-to-adult survival (viability),survival,survival,include_2,cor,0.36,NA,NA,NA,NA,NA,NA,NA,NA,"at-equator (pop RG, GA)",table s6,survival,survival,genotype,0.376885901,15,1,0.376885901,female,cross,Insecta,within
794,Drosophila melanogaster,46,rayyan-697471387,Spatially varying selection shapes life history clines among populations of Drosophila melanogaster from sub-Saharan Africa,2015,2002-2011,tropical and subtropical sub-Saharan populations,lab,female,female,NA,NA,26,26,NA,NA,NA,NA,286,176,line_mean_correlation,genetic_line,no,broad,CC,adult,adult,thorax length of 1 to 3 day odd adult females,fecundity 1-5 days (number of egg laid),size,fertility,include_2,cor,0.29,NA,NA,NA,NA,NA,NA,NA,NA,"below-equator (pop SF, SP, SE)",table s6,size,fertility,genotype,0.298566264,26,1,0.298566264,female,adult,Insecta,between
795,Drosophila melanogaster,46,rayyan-697471387,Spatially varying selection shapes life history clines among populations of Drosophila melanogaster from sub-Saharan Africa,2015,2002-2011,tropical and subtropical sub-Saharan populations,lab,female,female,NA,NA,26,26,NA,NA,NA,NA,286,145,line_mean_correlation,genetic_line,no,broad,CC,adult,adult,thorax length of 1 to 3 day odd adult females,fecundity 6-10 days (number of egg laid),size,fertility,include_2,cor,0.05,NA,NA,NA,NA,NA,NA,NA,NA,"below-equator (pop SF, SP, SE)",table s6,size,fertility,genotype,0.050041729,26,1,0.050041729,female,adult,Insecta,between
796,Drosophila melanogaster,368,rayyan-697472840,"Life history variation in an artificially selected population of drosophila melanogaster: Pleiotropy, superflies, and age-specific adaptation",2010,NA,NA,lab,female,female,NA,NA,58,58,NA,NA,NA,NA,NA,NA,line_mean_correlation,genetic_line,yes,broad,authors,both,adult,female lifespan,daily fecundity,survival,fertility,include,cor,-0.168,NA,NA,NA,NA,NA,NA,NA,NA,female_raw_all_daily_18,figure 5,survival,fertility,genotype,-0.169607861,58,1,-0.169607861,female,cross,Insecta,between
797,Drosophila melanogaster,368,rayyan-697472840,"Life history variation in an artificially selected population of drosophila melanogaster: Pleiotropy, superflies, and age-specific adaptation",2010,NA,NA,lab,female,female,NA,NA,58,58,NA,NA,NA,NA,NA,NA,line_mean_correlation,genetic_line,yes,broad,authors,both,adult,female lifespan,daily fecundity,survival,fertility,include,cor,-0.176,NA,NA,NA,NA,NA,NA,NA,NA,female_raw_all_daily_19,figure 5,survival,fertility,genotype,-0.177851799,58,1,-0.177851799,female,cross,Insecta,between
798,Drosophila melanogaster,368,rayyan-697472840,"Life history variation in an artificially selected population of drosophila melanogaster: Pleiotropy, superflies, and age-specific adaptation",2010,NA,NA,lab,female,female,NA,NA,58,58,NA,NA,NA,NA,NA,NA,line_mean_correlation,genetic_line,yes,broad,authors,both,adult,female lifespan,daily fecundity,survival,fertility,include,cor,-0.211,NA,NA,NA,NA,NA,NA,NA,NA,female_raw_all_daily_20,figure 5,survival,fertility,genotype,-0.214217711,58,1,-0.214217711,female,cross,Insecta,between
799,Drosophila melanogaster,368,rayyan-697472840,"Life history variation in an artificially selected population of drosophila melanogaster: Pleiotropy, superflies, and age-specific adaptation",2010,NA,NA,lab,female,female,NA,NA,58,58,NA,NA,NA,NA,NA,NA,line_mean_correlation,genetic_line,yes,broad,authors,both,adult,female lifespan,daily fecundity,survival,fertility,include,cor,-0.206,NA,NA,NA,NA,NA,NA,NA,NA,female_raw_all_daily_21,figure 5,survival,fertility,genotype,-0.208990458,58,1,-0.208990458,female,cross,Insecta,between
800,Drosophila melanogaster,368,rayyan-697472840,"Life history variation in an artificially selected population of drosophila melanogaster: Pleiotropy, superflies, and age-specific adaptation",2010,NA,NA,lab,female,female,NA,NA,58,58,NA,NA,NA,NA,NA,NA,line_mean_correlation,genetic_line,yes,broad,authors,both,adult,female lifespan,daily fecundity,survival,fertility,include,cor,-0.119,NA,NA,NA,NA,NA,NA,NA,NA,female_raw_all_daily_22,figure 5,survival,fertility,genotype,-0.119566541,58,1,-0.119566541,female,cross,Insecta,between
801,Drosophila melanogaster,368,rayyan-697472840,"Life history variation in an artificially selected population of drosophila melanogaster: Pleiotropy, superflies, and age-specific adaptation",2010,NA,NA,lab,female,female,NA,NA,58,58,NA,NA,NA,NA,NA,NA,line_mean_correlation,genetic_line,yes,broad,authors,both,adult,female lifespan,daily fecundity,survival,fertility,include,cor,-0.021,NA,NA,NA,NA,NA,NA,NA,NA,female_raw_all_daily_23,figure 5,survival,fertility,genotype,-0.021003088,58,1,-0.021003088,female,cross,Insecta,between
802,Drosophila melanogaster,368,rayyan-697472840,"Life history variation in an artificially selected population of drosophila melanogaster: Pleiotropy, superflies, and age-specific adaptation",2010,NA,NA,lab,female,female,NA,NA,58,58,NA,NA,NA,NA,NA,NA,line_mean_correlation,genetic_line,yes,broad,authors,both,adult,female lifespan,daily fecundity,survival,fertility,include,cor,0.124,NA,NA,NA,NA,NA,NA,NA,NA,female_raw_all_daily_24,figure 5,survival,fertility,genotype,0.12464147,58,1,0.12464147,female,cross,Insecta,between
803,Drosophila melanogaster,368,rayyan-697472840,"Life history variation in an artificially selected population of drosophila melanogaster: Pleiotropy, superflies, and age-specific adaptation",2010,NA,NA,lab,female,female,NA,NA,58,58,NA,NA,NA,NA,NA,NA,line_mean_correlation,genetic_line,yes,broad,authors,both,adult,female lifespan,daily fecundity,survival,fertility,include,cor,0.015,NA,NA,NA,NA,NA,NA,NA,NA,female_raw_all_daily_25,figure 5,survival,fertility,genotype,0.015001125,58,1,0.015001125,female,cross,Insecta,between
804,Drosophila melanogaster,368,rayyan-697472840,"Life history variation in an artificially selected population of drosophila melanogaster: Pleiotropy, superflies, and age-specific adaptation",2010,NA,NA,lab,female,female,NA,NA,58,58,NA,NA,NA,NA,NA,NA,line_mean_correlation,genetic_line,yes,broad,authors,both,adult,female lifespan,daily fecundity,survival,fertility,include,cor,-0.01,NA,NA,NA,NA,NA,NA,NA,NA,female_raw_all_daily_26,figure 5,survival,fertility,genotype,-0.010000333,58,1,-0.010000333,female,cross,Insecta,between
805,Drosophila melanogaster,368,rayyan-697472840,"Life history variation in an artificially selected population of drosophila melanogaster: Pleiotropy, superflies, and age-specific adaptation",2010,NA,NA,lab,female,female,NA,NA,58,58,NA,NA,NA,NA,NA,NA,line_mean_correlation,genetic_line,yes,broad,authors,both,adult,female lifespan,daily fecundity,survival,fertility,include,cor,-0.038,NA,NA,NA,NA,NA,NA,NA,NA,female_raw_all_daily_27,figure 5,survival,fertility,genotype,-0.038018307,58,1,-0.038018307,female,cross,Insecta,between
806,Drosophila melanogaster,153,rayyan-697472360,Age-specific patterns of genetic variance in Drosophila melanogaster .2. Fecundity and its genetic covariance with age-specific mortality,1996,1981,NA,lab,female,female,50,50,10,10,50,50,50,50,NA,NA,animal_model,genetic_line,no,narrow,authors,adult,adult,fertility in day 10,fertility in day 14,fertility,fertility,include,cor,NA,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-697472360,fig 3,fertility,fertility,genotype,NA,10,1,NA,female,adult,Insecta,within
807,Drosophila melanogaster,153,rayyan-697472360,Age-specific patterns of genetic variance in Drosophila melanogaster .2. Fecundity and its genetic covariance with age-specific mortality,1996,1981,NA,lab,female,female,50,50,10,10,50,50,50,50,NA,NA,animal_model,genetic_line,no,narrow,authors,adult,adult,fertility in day 10,fertility in day 17,fertility,fertility,include,cor,0.674,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-697472360,fig 3,fertility,fertility,genotype,0.818036935,10,1,0.818036935,female,adult,Insecta,within
808,Drosophila melanogaster,153,rayyan-697472360,Age-specific patterns of genetic variance in Drosophila melanogaster .2. Fecundity and its genetic covariance with age-specific mortality,1996,1981,NA,lab,female,female,50,50,10,10,50,50,50,50,NA,NA,animal_model,genetic_line,no,narrow,authors,adult,adult,fertility in day 10,fertility in day 21,fertility,fertility,include,cor,0.242,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-697472360,fig 3,fertility,fertility,genotype,0.246897438,10,1,0.246897438,female,adult,Insecta,within
809,Drosophila melanogaster,153,rayyan-697472360,Age-specific patterns of genetic variance in Drosophila melanogaster .2. Fecundity and its genetic covariance with age-specific mortality,1996,1981,NA,lab,female,female,50,50,10,10,50,50,50,50,NA,NA,animal_model,genetic_line,no,narrow,authors,adult,adult,fertility in day 10,fertility in day 24,fertility,fertility,include,cor,0.075,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-697472360,fig 3,fertility,fertility,genotype,0.075141102,10,1,0.075141102,female,adult,Insecta,within
810,Drosophila melanogaster,153,rayyan-697472360,Age-specific patterns of genetic variance in Drosophila melanogaster .2. Fecundity and its genetic covariance with age-specific mortality,1996,1981,NA,lab,female,female,50,50,10,10,50,50,50,50,NA,NA,animal_model,genetic_line,no,narrow,authors,adult,adult,fertility in day 10,fertility in day 28,fertility,fertility,include,cor,-0.092,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-697472360,fig 3,fertility,fertility,genotype,-0.092260889,10,1,-0.092260889,female,adult,Insecta,within
811,Drosophila melanogaster,153,rayyan-697472360,Age-specific patterns of genetic variance in Drosophila melanogaster .2. Fecundity and its genetic covariance with age-specific mortality,1996,1981,NA,lab,female,female,50,50,10,10,50,50,50,50,NA,NA,animal_model,genetic_line,no,narrow,authors,adult,adult,fertility in day 10,fertility in day 31,fertility,fertility,include,cor,-0.253,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-697472360,fig 3,fertility,fertility,genotype,-0.258615385,10,1,-0.258615385,female,adult,Insecta,within
812,Drosophila melanogaster,331,rayyan-697472553,Genetic variation but weak genetic covariation between pre- and post-copulatory episodes of sexual selection in Drosophila melanogaster,2016,2013,"Margaret  River, Western Australia",lab,male,male,NA,NA,39,34,NA,NA,NA,NA,249.6,95.2,line_mean_correlation,genetic_line,no,broad,CC,adult,adult,male mating success,offensive spearm competitiveness,fertility,fertility,include,cor,0.15,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-697472553,figure 2,fertility,fertility,genotype,0.151140436,34,1,0.151140436,male,adult,Insecta,within
813,Drosophila melanogaster,331,rayyan-697472553,Genetic variation but weak genetic covariation between pre- and post-copulatory episodes of sexual selection in Drosophila melanogaster,2016,2013,"Margaret  River, Western Australia",lab,male,male,NA,NA,39,38,NA,NA,NA,NA,249.6,171,line_mean_correlation,genetic_line,no,broad,CC,adult,adult,male mating success,male wing size,fertility,size,include,cor,0.04,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-697472553,figure 2,fertility,size,genotype,0.040021354,38,1,0.040021354,male,adult,Insecta,between
814,Drosophila melanogaster,331,rayyan-697472553,Genetic variation but weak genetic covariation between pre- and post-copulatory episodes of sexual selection in Drosophila melanogaster,2016,2013,"Margaret  River, Western Australia",lab,male,male,NA,NA,34,38,NA,NA,NA,NA,95.2,171,line_mean_correlation,genetic_line,no,broad,CC,adult,adult,offensive sperm competitiveness,male wing size,fertility,size,include,cor,0.32,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-697472553,figure 2,fertility,size,genotype,0.331647109,34,1,0.331647109,male,adult,Insecta,between
817,Drosophila melanogaster,153,rayyan-697472360,Age-specific patterns of genetic variance in Drosophila melanogaster .2. Fecundity and its genetic covariance with age-specific mortality,1996,1981,NA,lab,female,female,50,50,10,10,50,50,50,50,NA,NA,animal_model,genetic_line,no,narrow,authors,adult,adult,fertility in day 21,fertility in day 28,fertility,fertility,include,cor,0.949,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-697472360,fig 3,fertility,fertility,genotype,1.821623033,10,1,1.821623033,female,adult,Insecta,within
818,Drosophila melanogaster,153,rayyan-697472360,Age-specific patterns of genetic variance in Drosophila melanogaster .2. Fecundity and its genetic covariance with age-specific mortality,1996,1981,NA,lab,female,female,50,50,10,10,50,50,50,50,NA,NA,animal_model,genetic_line,no,narrow,authors,adult,adult,fertility in day 21,fertility in day 31,fertility,fertility,include,cor,0.998,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-697472360,fig 3,fertility,fertility,genotype,3.453377389,10,1,3.453377389,female,adult,Insecta,within
820,Drosophila melanogaster,153,rayyan-697472360,Age-specific patterns of genetic variance in Drosophila melanogaster .2. Fecundity and its genetic covariance with age-specific mortality,1996,1981,NA,lab,female,female,50,50,10,10,50,50,50,50,NA,NA,animal_model,genetic_line,no,narrow,authors,adult,adult,fertility in day 24,fertility in day 31,fertility,fertility,include,cor,0.367,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-697472360,fig 3,fertility,fertility,genotype,0.384951707,10,1,0.384951707,female,adult,Insecta,within
821,Drosophila melanogaster,153,rayyan-697472360,Age-specific patterns of genetic variance in Drosophila melanogaster .2. Fecundity and its genetic covariance with age-specific mortality,1996,1981,NA,lab,female,female,50,50,10,10,50,50,50,50,NA,NA,animal_model,genetic_line,no,narrow,authors,adult,adult,fertility in day 28,fertility in day 31,fertility,fertility,include,cor,NA,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-697472360,fig 3,fertility,fertility,genotype,NA,10,1,NA,female,adult,Insecta,within
822,Drosophila melanogaster,154,rayyan-697472367,THE EVOLUTIONARY GENETICS OF MALE LIFE-HISTORY CHARACTERS IN DROSOPHILA-MELANOGASTER,1995,1975,Amherst,lab,male,male,320,320,40,40,960,960,960,960,3017,3580,matrix,genetic_line,no,narrow,authors,adult,adult,body mass,early male mating ability,size,fertility,include,cor,-0.808,1.573,se,NA,NA,NA,NA,NA,NA,rayyan-697472367,table 7,size,fertility,genotype,-1.121240584,40,1,-1.121240584,male,adult,Insecta,between
823,Drosophila melanogaster,154,rayyan-697472367,THE EVOLUTIONARY GENETICS OF MALE LIFE-HISTORY CHARACTERS IN DROSOPHILA-MELANOGASTER,1995,1975,Amherst,lab,male,male,320,320,40,40,960,960,960,960,3017,3510,matrix,genetic_line,no,narrow,authors,adult,adult,body mass,late male mating ability,size,fertility,include,cor,-0.061,0.42,se,NA,NA,NA,NA,NA,NA,rayyan-697472367,table 7,size,fertility,genotype,-0.06107583,40,1,-0.06107583,male,adult,Insecta,between
826,Drosophila melanogaster,154,rayyan-697472367,THE EVOLUTIONARY GENETICS OF MALE LIFE-HISTORY CHARACTERS IN DROSOPHILA-MELANOGASTER,1995,1975,Amherst,lab,male,male,320,320,40,40,960,960,960,960,3017,6876,matrix,genetic_line,no,narrow,authors,adult,both,body mass,mean longevity ,size,survival,include,cor,0.234,0.201,se,NA,NA,NA,NA,NA,NA,rayyan-697472367,table 7,size,survival,genotype,0.238417017,40,1,0.238417017,male,cross,Insecta,between
827,Drosophila melanogaster,154,rayyan-697472367,THE EVOLUTIONARY GENETICS OF MALE LIFE-HISTORY CHARACTERS IN DROSOPHILA-MELANOGASTER,1995,1975,Amherst,lab,male,male,320,320,40,40,960,960,960,960,3580,3510,matrix,genetic_line,no,narrow,authors,adult,adult,early male mating ability (number of mating),late male mating ability,fertility,fertility,include,cor,0.041,0.142,se,NA,NA,NA,NA,NA,NA,rayyan-697472367,table 7,fertility,fertility,genotype,0.041022997,40,1,0.041022997,male,adult,Insecta,within
829,Drosophila melanogaster,154,rayyan-697472367,THE EVOLUTIONARY GENETICS OF MALE LIFE-HISTORY CHARACTERS IN DROSOPHILA-MELANOGASTER,1995,1975,Amherst,lab,male,male,320,320,40,40,960,960,960,960,3580,6876,matrix,genetic_line,no,narrow,authors,adult,both,early male mating ability (number of mating),intercept of mortality,fertility,reverse_survival,include,cor,0.951,2.17,se,NA,NA,NA,NA,NA,NA,rayyan-697472367,table 7,fertility,survival,genotype,1.842138521,40,-1,-1.842138521,male,cross,Insecta,between
830,Drosophila melanogaster,154,rayyan-697472367,THE EVOLUTIONARY GENETICS OF MALE LIFE-HISTORY CHARACTERS IN DROSOPHILA-MELANOGASTER,1995,1975,Amherst,lab,male,male,320,320,40,40,960,960,960,960,3580,6876,matrix,genetic_line,no,narrow,authors,adult,both,early male mating ability (number of mating),mean longevity ,fertility,survival,include,cor,-0.044,0.642,se,NA,NA,NA,NA,NA,NA,rayyan-697472367,table 7,fertility,survival,genotype,-0.044028428,40,1,-0.044028428,male,cross,Insecta,between
832,Drosophila melanogaster,154,rayyan-697472367,THE EVOLUTIONARY GENETICS OF MALE LIFE-HISTORY CHARACTERS IN DROSOPHILA-MELANOGASTER,1995,1975,Amherst,lab,male,male,320,320,40,40,960,960,960,960,3510,6876,matrix,genetic_line,no,narrow,authors,adult,both,late male mating ability (number of mating),intercept of mortality,fertility,reverse_survival,include,cor,0.074,0.094,se,NA,NA,NA,NA,NA,NA,rayyan-697472367,table 7,fertility,survival,genotype,0.07413552,40,-1,-0.07413552,male,cross,Insecta,between
833,Drosophila melanogaster,154,rayyan-697472367,THE EVOLUTIONARY GENETICS OF MALE LIFE-HISTORY CHARACTERS IN DROSOPHILA-MELANOGASTER,1995,1975,Amherst,lab,male,male,320,320,40,40,960,960,960,960,3510,6876,matrix,genetic_line,no,narrow,authors,adult,both,late male mating ability (number of mating),mean longevity ,fertility,survival,include,cor,0.225,0.06,se,NA,NA,NA,NA,NA,NA,rayyan-697472367,table 7,fertility,survival,genotype,0.228916547,40,1,0.228916547,male,cross,Insecta,between
834,Drosophila melanogaster,125,rayyan-697471866,Effects on fitness components of P-element inserts in Drosophila melanogaster: Analysis of trade-offs,1996,NA,NA,lab,both,both,NA,NA,12,12,NA,NA,NA,NA,720,720,line_mean_correlation,genetic_line,no,broad,CC,adult,adult,birth rate in the first five days after eclosion,birth rate in the 5-10 days after eclosion,fertility,fertility,include,cor,0.348958333,NA,NA,NA,NA,NA,NA,NA,NA,25,figure 5a,fertility,fertility,genotype,0.364257162,12,1,0.364257162,both,adult,Insecta,within
835,Drosophila melanogaster,125,rayyan-697471866,Effects on fitness components of P-element inserts in Drosophila melanogaster: Analysis of trade-offs,1996,NA,NA,lab,both,both,NA,NA,12,12,NA,NA,NA,NA,720,720,line_mean_correlation,genetic_line,no,broad,CC,adult,adult,birth rate in the first five days after eclosion,birth rate in the 10-15 days after eclosion,fertility,fertility,include,cor,-0.765625,NA,NA,NA,NA,NA,NA,NA,NA,25,figure 5a,fertility,fertility,genotype,-1.009668809,12,1,-1.009668809,both,adult,Insecta,within
836,Drosophila melanogaster,125,rayyan-697471866,Effects on fitness components of P-element inserts in Drosophila melanogaster: Analysis of trade-offs,1996,NA,NA,lab,both,both,NA,NA,12,12,NA,NA,NA,NA,720,720,line_mean_correlation,genetic_line,no,broad,CC,adult,adult,birth rate in the first five days after eclosion,birth rate in the 15-20 days after eclosion,fertility,fertility,include,cor,-0.776041667,NA,NA,NA,NA,NA,NA,NA,NA,25,figure 5a,fertility,fertility,genotype,-1.035341182,12,1,-1.035341182,both,adult,Insecta,within
837,Drosophila melanogaster,125,rayyan-697471866,Effects on fitness components of P-element inserts in Drosophila melanogaster: Analysis of trade-offs,1996,NA,NA,lab,both,both,NA,NA,12,12,NA,NA,NA,NA,720,720,line_mean_correlation,genetic_line,no,broad,CC,adult,adult,birth rate in the first five days after eclosion,birth rate in the 20-25 days after eclosion,fertility,fertility,include,cor,-0.536458333,NA,NA,NA,NA,NA,NA,NA,NA,25,figure 5a,fertility,fertility,genotype,-0.599169493,12,1,-0.599169493,both,adult,Insecta,within
840,Drosophila melanogaster,225,rayyan-197247314,Genetic variation and the role of insect life history traits in the ability of Drosophila larvae to develop in the presence of a competing filamentous fungus,2006,2004,"Kiel, Germany",lab,both,both,NA,NA,17,17,340,340,340,340,340,340,line_mean_correlation,genetic_line,no,broad,CC,non_adult,non_adult,survival of larval on uninfected patched,developmental time,survival,reverse_maturation,include,cor,-0.042,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-197247314,genetic correlations,survival,maturation,genotype,-0.042024722,17,-1,0.042024722,both,non_adult,Insecta,between
841,Drosophila melanogaster,225,rayyan-197247314,Genetic variation and the role of insect life history traits in the ability of Drosophila larvae to develop in the presence of a competing filamentous fungus,2006,2004,"Kiel, Germany",lab,both,both,NA,NA,17,17,340,340,340,340,340,340,line_mean_correlation,genetic_line,no,broad,CC,non_adult,adult,survival of larval on uninfected patched,adult body weight,survival,size,include,cor,0.244,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-197247314,genetic correlations,survival,size,genotype,0.249022949,17,1,0.249022949,both,cross,Insecta,between
842,Drosophila melanogaster,225,rayyan-197247314,Genetic variation and the role of insect life history traits in the ability of Drosophila larvae to develop in the presence of a competing filamentous fungus,2006,2004,"Kiel, Germany",lab,both,both,NA,NA,17,17,340,340,340,340,340,340,line_mean_correlation,genetic_line,no,broad,CC,non_adult,adult,developmental time,adult body weight,reverse_maturation,size,include,cor,0.181,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-197247314,genetic correlations,maturation,size,genotype,0.183016366,17,-1,-0.183016366,both,cross,Insecta,between
843,Drosophila melanogaster,231,rayyan-197247345,"Pleiotropic effects of methoprene-tolerant (Met), a gene involved in juvenile hormone metabolism, on life history traits in Drosophila melanogaster",2004,NA,NA,lab,female,female,20,20,10,10,NA,NA,NA,NA,NA,NA,line_mean_correlation,genetic_line,no,NA,NA,non_adult,adult,development time,early fecundity,reverse_maturation,fertility,include,cor,-0.84,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-197247345,"allelic effects on trait relationships, second para",maturation,fertility,genotype,-1.221173518,10,-1,1.221173518,female,cross,Insecta,between
844,Drosophila melanogaster,236,rayyan-197247373,The devil in the details of life-history evolution: Instability and reversal of genetic correlations during selection on Drosophila development,2003,1975-1991,Massachusetts,lab,male,male,NA,NA,55,55,NA,NA,NA,NA,11000,3300,line_mean_correlation,genetic_line,yes,broad,CC,non_adult,adult,development time,body size (dry weight at emergence),reverse_maturation,size,include,cor,0.865,NA,NA,NA,NA,NA,NA,NA,NA,male_all,Correlations among characters,maturation,size,genotype,1.312870777,55,-1,-1.312870777,male,cross,Insecta,between
845,Drosophila melanogaster,236,rayyan-197247373,The devil in the details of life-history evolution: Instability and reversal of genetic correlations during selection on Drosophila development,2003,1975-1991,Massachusetts,lab,female,female,NA,NA,55,55,NA,NA,NA,NA,11000,3300,line_mean_correlation,genetic_line,yes,broad,CC,non_adult,adult,development time,body size (dry weight at emergence),reverse_maturation,size,include,cor,0.854,NA,NA,NA,NA,NA,NA,NA,NA,female_all,Correlations among characters,maturation,size,genotype,1.270747062,55,-1,-1.270747062,female,cross,Insecta,between
848,Drosophila melanogaster,236,rayyan-197247373,The devil in the details of life-history evolution: Instability and reversal of genetic correlations during selection on Drosophila development,2003,1975-1991,Massachusetts,lab,both,both,NA,NA,55,55,NA,NA,NA,NA,6600,11000,line_mean_correlation,genetic_line,yes,broad,CC,non_adult,non_adult,growth rate,viability (egg to adult),growth,survival,include,cor,0.385,NA,NA,NA,NA,NA,NA,NA,NA,all,Correlations among characters,growth,survival,genotype,0.405916575,55,1,0.405916575,both,non_adult,Insecta,between
849,Drosophila melanogaster,236,rayyan-197247373,The devil in the details of life-history evolution: Instability and reversal of genetic correlations during selection on Drosophila development,2003,1975-1991,Massachusetts,lab,both,both,NA,NA,45,45,NA,NA,NA,NA,5400,9000,line_mean_correlation,genetic_line,yes,broad,CC,non_adult,non_adult,growth rate,viability (egg to adult),growth,survival,include,cor,0.618,NA,NA,NA,NA,NA,NA,NA,NA,all_acb_aco_removed,Correlations among characters,growth,survival,genotype,0.721762745,45,1,0.721762745,both,non_adult,Insecta,between
850,Drosophila melanogaster,392,rayyan-697472974,Genetic variance for diapause expression and associated life histories in Drosophila melanogaster,2005,2001,"Walpole, Maine, USA",lab,female,female,NA,NA,30,30,NA,NA,NA,NA,600,600,line_mean_correlation,genetic_line,no,broad,CC,adult,adult,eggs/female days 1-7,eggs/female days 8-15,fertility,fertility,include,cor,0.516,NA,NA,NA,NA,NA,NA,NA,NA,diapause,table 4,fertility,fertility,genotype,0.57087283,30,1,0.57087283,female,adult,Insecta,within
851,Drosophila melanogaster,410,rayyan-697473214,Effects of larval crowding on quantitative variation for development time and viability in Drosophila melanogaster,2016,NA,NA,lab,both,both,NA,NA,31,31,NA,NA,NA,NA,5957,5957,line_mean_correlation,genetic_line,no,broad,CC,non_adult,adult,development time,adult-to-adult competitive reproductive fitness (the number of the offspring of this genotype to the total number of progeny emerged),reverse_maturation,fertility,include,cor,-0.56,NA,NA,NA,NA,NA,NA,NA,NA,high,result_3.8,maturation,fertility,genotype,-0.632833187,31,-1,0.632833187,both,cross,Insecta,between
852,Drosophila melanogaster,410,rayyan-697473214,Effects of larval crowding on quantitative variation for development time and viability in Drosophila melanogaster,2016,NA,NA,lab,both,both,NA,NA,31,31,NA,NA,NA,NA,2637,2637,line_mean_correlation,genetic_line,no,broad,CC,non_adult,adult,development time,adult-to-adult competitive reproductive fitness (the number of the offspring of this genotype to the total number of progeny emerged),reverse_maturation,fertility,include,cor,-0.54,NA,NA,NA,NA,NA,NA,NA,NA,medium,result_3.8,maturation,fertility,genotype,-0.604155603,31,-1,0.604155603,both,cross,Insecta,between
853,Drosophila melanogaster,410,rayyan-697473214,Effects of larval crowding on quantitative variation for development time and viability in Drosophila melanogaster,2016,NA,NA,lab,both,both,NA,NA,31,31,NA,NA,NA,NA,1685,1685,line_mean_correlation,genetic_line,no,broad,CC,non_adult,adult,development time,adult-to-adult competitive reproductive fitness (the number of the offspring of this genotype to the total number of progeny emerged),reverse_maturation,fertility,include,cor,0.19,NA,NA,NA,NA,NA,NA,NA,NA,low,result_3.8,maturation,fertility,genotype,0.192337169,31,-1,-0.192337169,both,cross,Insecta,between
854,Drosophila melanogaster,410,rayyan-697473214,Effects of larval crowding on quantitative variation for development time and viability in Drosophila melanogaster,2016,NA,NA,lab,both,both,NA,NA,31,31,NA,NA,NA,NA,5957,5957,line_mean_correlation,genetic_line,no,broad,CC,non_adult,adult,egg-adult-viability,adult-to-adult competitive reproductive fitness (the number of the offspring of this genotype to the total number of progeny emerged),survival,fertility,include,cor,0.26,NA,NA,NA,NA,NA,NA,NA,NA,high,result_3.8,survival,fertility,genotype,0.266108407,31,1,0.266108407,both,cross,Insecta,between
855,Drosophila melanogaster,410,rayyan-697473214,Effects of larval crowding on quantitative variation for development time and viability in Drosophila melanogaster,2016,NA,NA,lab,both,both,NA,NA,31,31,NA,NA,NA,NA,2637,2637,line_mean_correlation,genetic_line,no,broad,CC,non_adult,adult,egg-adult-viability,adult-to-adult competitive reproductive fitness (the number of the offspring of this genotype to the total number of progeny emerged),survival,fertility,include,cor,0.17,NA,NA,NA,NA,NA,NA,NA,NA,medium,result_3.8,survival,fertility,genotype,0.171666664,31,1,0.171666664,both,cross,Insecta,between
856,Drosophila melanogaster,410,rayyan-697473214,Effects of larval crowding on quantitative variation for development time and viability in Drosophila melanogaster,2016,NA,NA,lab,both,both,NA,NA,31,31,NA,NA,NA,NA,1685,1685,line_mean_correlation,genetic_line,no,broad,CC,non_adult,adult,egg-adult-viability,adult-to-adult competitive reproductive fitness (the number of the offspring of this genotype to the total number of progeny emerged),survival,fertility,include,cor,0.16,NA,NA,NA,NA,NA,NA,NA,NA,low,result_3.8,survival,fertility,genotype,0.161386696,31,1,0.161386696,both,cross,Insecta,between
857,Drosophila melanogaster,125,rayyan-697471866,Effects on fitness components of P-element inserts in Drosophila melanogaster: Analysis of trade-offs,1996,NA,NA,lab,both,both,NA,NA,12,12,NA,NA,NA,NA,720,7200,line_mean_correlation,genetic_line,no,broad,CC,adult,both,birth rate in the first five days after eclosion,mortality in the 0-5 days,fertility,reverse_survival,include,cor,-0.308900524,NA,NA,NA,NA,NA,NA,NA,NA,29,figure 5b,fertility,survival,genotype,-0.319329498,12,-1,0.319329498,both,cross,Insecta,between
858,Drosophila melanogaster,125,rayyan-697471866,Effects on fitness components of P-element inserts in Drosophila melanogaster: Analysis of trade-offs,1996,NA,NA,lab,both,both,NA,NA,12,12,NA,NA,NA,NA,720,7200,line_mean_correlation,genetic_line,no,broad,CC,adult,both,birth rate in the first five days after eclosion,mortality in the 5-10 days,fertility,reverse_survival,include,cor,-0.303664921,NA,NA,NA,NA,NA,NA,NA,NA,29,figure 5b,fertility,survival,genotype,-0.313551884,12,-1,0.313551884,both,cross,Insecta,between
859,Drosophila melanogaster,46,rayyan-697471387,Spatially varying selection shapes life history clines among populations of Drosophila melanogaster from sub-Saharan Africa,2015,2002-2011,tropical and subtropical sub-Saharan populations,lab,female,both,NA,NA,39,38,NA,NA,NA,NA,233,2265,line_mean_correlation,genetic_line,no,broad,CC,adult,non_adult,fecundity 1-10 days (number of eggs laid),proportion egg-to-adult survival (viability),fertility,survival,include_2,cor,0.45,NA,NA,NA,NA,NA,NA,NA,NA,"above-equator (pop EF, ED, CO, EA, NG)",table s6,fertility,survival,genotype,0.484700279,38,1,0.484700279,female,cross,Insecta,between
860,Drosophila melanogaster,125,rayyan-697471866,Effects on fitness components of P-element inserts in Drosophila melanogaster: Analysis of trade-offs,1996,NA,NA,lab,both,both,NA,NA,12,12,NA,NA,NA,NA,720,7200,line_mean_correlation,genetic_line,no,broad,CC,adult,both,birth rate in the first five days after eclosion,mortality in the 15-20 days,fertility,reverse_survival,include,cor,0.32460733,NA,NA,NA,NA,NA,NA,NA,NA,29,figure 5b,fertility,survival,genotype,0.336788542,12,-1,-0.336788542,both,cross,Insecta,between
861,Drosophila melanogaster,125,rayyan-697471866,Effects on fitness components of P-element inserts in Drosophila melanogaster: Analysis of trade-offs,1996,NA,NA,lab,both,both,NA,NA,12,12,NA,NA,NA,NA,720,7200,line_mean_correlation,genetic_line,no,broad,CC,adult,both,birth rate in the first five days after eclosion,mortality in the 20-25 days,fertility,reverse_survival,include,cor,0.298429319,NA,NA,NA,NA,NA,NA,NA,NA,29,figure 5b,fertility,survival,genotype,0.307794473,12,-1,-0.307794473,both,cross,Insecta,between
862,Drosophila melanogaster,125,rayyan-697471866,Effects on fitness components of P-element inserts in Drosophila melanogaster: Analysis of trade-offs,1996,NA,NA,lab,both,both,NA,NA,12,12,NA,NA,NA,NA,720,7200,line_mean_correlation,genetic_line,no,broad,CC,adult,both,birth rate in the first five days after eclosion,mortality in the 25-30 days,fertility,reverse_survival,include,cor,-0.371727749,NA,NA,NA,NA,NA,NA,NA,NA,29,figure 5b,fertility,survival,genotype,-0.390426381,12,-1,0.390426381,both,cross,Insecta,between
863,Drosophila melanogaster,125,rayyan-697471866,Effects on fitness components of P-element inserts in Drosophila melanogaster: Analysis of trade-offs,1996,NA,NA,lab,both,both,NA,NA,12,12,NA,NA,NA,NA,720,7200,line_mean_correlation,genetic_line,no,broad,CC,adult,both,birth rate in the first five days after eclosion,mortality in the 30-35 days,fertility,reverse_survival,include,cor,-0.319371728,NA,NA,NA,NA,NA,NA,NA,NA,29,figure 5b,fertility,survival,genotype,-0.330947319,12,-1,0.330947319,both,cross,Insecta,between
864,Drosophila melanogaster,125,rayyan-697471866,Effects on fitness components of P-element inserts in Drosophila melanogaster: Analysis of trade-offs,1996,NA,NA,lab,both,both,NA,NA,12,12,NA,NA,NA,NA,720,7200,line_mean_correlation,genetic_line,no,broad,CC,adult,both,birth rate in the first five days after eclosion,mortality in the 35-40 days,fertility,reverse_survival,include,cor,-0.219895288,NA,NA,NA,NA,NA,NA,NA,NA,29,figure 5b,fertility,survival,genotype,-0.223546074,12,-1,0.223546074,both,cross,Insecta,between
869,Drosophila melanogaster,126,rayyan-697471867,The response to selection for fast larval development in Drosophila melanogaster and its effect on adult weight: An example of a fitness trade- off,1996,NA,California,lab,both,both,200,200,4,4,200,200,200,200,18000,18000,correlated_selection,genetic_line,yes,broad,authors,adult,non_adult,adult dry weight,larval development time ,size,reverse_maturation,include,cor,0.856,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-697471867,table 4,size,maturation,genotype,1.278182807,4,-1,-1.278182807,both,cross,Insecta,between
870,Drosophila melanogaster,153,rayyan-697472360,Age-specific patterns of genetic variance in Drosophila melanogaster .2. Fecundity and its genetic covariance with age-specific mortality,1996,1981,NA,lab,male,male,50,50,10,10,50,50,50,50,NA,NA,animal_model,genetic_line,no,narrow,authors,both,both,mortality in week 1,mortality in week 2,reverse_survival,reverse_survival,include,cor,NA,NA,NA,NA,NA,NA,NA,NA,NA,male,table 1,survival,survival,genotype,NA,10,1,NA,male,both,Insecta,within
871,Drosophila melanogaster,153,rayyan-697472360,Age-specific patterns of genetic variance in Drosophila melanogaster .2. Fecundity and its genetic covariance with age-specific mortality,1996,1981,NA,lab,male,male,50,50,10,10,50,50,50,50,NA,NA,animal_model,genetic_line,no,narrow,authors,both,both,mortality in week 1,mortality in week 3,reverse_survival,reverse_survival,include,cor,0.6454,NA,NA,NA,NA,NA,NA,NA,NA,male,table 1,survival,survival,genotype,0.767374201,10,1,0.767374201,male,both,Insecta,within
872,Drosophila melanogaster,153,rayyan-697472360,Age-specific patterns of genetic variance in Drosophila melanogaster .2. Fecundity and its genetic covariance with age-specific mortality,1996,1981,NA,lab,male,male,50,50,10,10,50,50,50,50,NA,NA,animal_model,genetic_line,no,narrow,authors,both,both,mortality in week 1,mortality in week 4,reverse_survival,reverse_survival,include,cor,0.937,NA,NA,NA,NA,NA,NA,NA,NA,male,table 1,survival,survival,genotype,1.712880469,10,1,1.712880469,male,both,Insecta,within
873,Drosophila melanogaster,153,rayyan-697472360,Age-specific patterns of genetic variance in Drosophila melanogaster .2. Fecundity and its genetic covariance with age-specific mortality,1996,1981,NA,lab,male,male,50,50,10,10,50,50,50,50,NA,NA,animal_model,genetic_line,no,narrow,authors,both,both,mortality in week 1,mortality in week 5,reverse_survival,reverse_survival,include,cor,0.777,NA,NA,NA,NA,NA,NA,NA,NA,male,table 1,survival,survival,genotype,1.037755028,10,1,1.037755028,male,both,Insecta,within
874,Drosophila melanogaster,153,rayyan-697472360,Age-specific patterns of genetic variance in Drosophila melanogaster .2. Fecundity and its genetic covariance with age-specific mortality,1996,1981,NA,lab,male,male,50,50,10,10,50,50,50,50,NA,NA,animal_model,genetic_line,no,narrow,authors,both,both,mortality in week 1,mortality in week 6,reverse_survival,reverse_survival,include,cor,0.778,NA,NA,NA,NA,NA,NA,NA,NA,male,table 1,survival,survival,genotype,1.040283517,10,1,1.040283517,male,both,Insecta,within
875,Drosophila melanogaster,153,rayyan-697472360,Age-specific patterns of genetic variance in Drosophila melanogaster .2. Fecundity and its genetic covariance with age-specific mortality,1996,1981,NA,lab,male,male,50,50,10,10,50,50,50,50,NA,NA,animal_model,genetic_line,no,narrow,authors,both,both,mortality in week 1,mortality in week 7,reverse_survival,reverse_survival,include,cor,0.723,NA,NA,NA,NA,NA,NA,NA,NA,male,table 1,survival,survival,genotype,0.913902365,10,1,0.913902365,male,both,Insecta,within
877,Drosophila melanogaster,258,rayyan-197247442,Spontaneous mutation for life-history traits in Drosophila melanogaster,1998,NA,NA,lab,female,female,NA,NA,6,6,NA,NA,NA,NA,NA,NA,line_mean_correlation,genetic_line,no,broad,authors,non_adult,adult,early viability  (percentage of eggs developing into pupae),late fecundity (number of eggs),survival,fertility,include,cor,0.53,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-197247442,table 6,survival,fertility,genotype,0.59014516,6,1,0.59014516,female,cross,Insecta,between
878,Drosophila melanogaster,258,rayyan-197247442,Spontaneous mutation for life-history traits in Drosophila melanogaster,1998,NA,NA,lab,female,female,NA,NA,6,6,NA,NA,NA,NA,NA,NA,line_mean_correlation,genetic_line,no,broad,authors,non_adult,non_adult,early viability  (percentage of eggs developing into pupae),late viability (percentage of eggs developing into pupae),survival,survival,include,cor,0.4,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-197247442,table 6,survival,survival,genotype,0.42364893,6,1,0.42364893,female,non_adult,Insecta,within
879,Drosophila melanogaster,258,rayyan-197247442,Spontaneous mutation for life-history traits in Drosophila melanogaster,1998,NA,NA,lab,female,female,NA,NA,6,6,NA,NA,NA,NA,NA,NA,line_mean_correlation,genetic_line,no,broad,authors,non_adult,adult,early viability  (percentage of eggs developing into pupae),late pupal productivity (number of pupae produced),survival,fertility,include,cor,0.65,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-197247442,table 6,survival,fertility,genotype,0.775298706,6,1,0.775298706,female,cross,Insecta,between
881,Drosophila melanogaster,258,rayyan-197247442,Spontaneous mutation for life-history traits in Drosophila melanogaster,1998,NA,NA,lab,female,female,NA,NA,6,6,NA,NA,NA,NA,NA,NA,line_mean_correlation,genetic_line,no,broad,authors,adult,adult,early pupal productivity (number of pupae produced),late fecundity (number of eggs),fertility,fertility,include,cor,0.61,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-197247442,table 6,fertility,fertility,genotype,0.708921359,6,1,0.708921359,female,adult,Insecta,within
882,Drosophila melanogaster,258,rayyan-197247442,Spontaneous mutation for life-history traits in Drosophila melanogaster,1998,NA,NA,lab,female,female,NA,NA,6,6,NA,NA,NA,NA,NA,NA,line_mean_correlation,genetic_line,no,broad,authors,adult,non_adult,early pupal productivity (number of pupae produced),late viability (percentage of eggs developing into pupae),fertility,survival,include,cor,0.59,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-197247442,table 6,fertility,survival,genotype,0.677666068,6,1,0.677666068,female,cross,Insecta,between
883,Drosophila melanogaster,258,rayyan-197247442,Spontaneous mutation for life-history traits in Drosophila melanogaster,1998,NA,NA,lab,female,female,NA,NA,6,6,NA,NA,NA,NA,NA,NA,line_mean_correlation,genetic_line,no,broad,authors,adult,adult,early pupal productivity (number of pupae produced),late pupal productivity (number of pupae produced),fertility,fertility,include,cor,0.81,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-197247442,table 6,fertility,fertility,genotype,1.127029026,6,1,1.127029026,female,adult,Insecta,within
887,Drosophila melanogaster,258,rayyan-197247442,Spontaneous mutation for life-history traits in Drosophila melanogaster,1998,NA,NA,lab,female,female,NA,NA,6,6,NA,NA,NA,NA,NA,NA,line_mean_correlation,genetic_line,no,broad,authors,adult,non_adult,late fecundity (number of eggs),late viability (percentage of eggs developing into pupae),fertility,survival,include,cor,0.11,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-197247442,table 6,fertility,survival,genotype,0.110446916,6,1,0.110446916,female,cross,Insecta,between
888,Drosophila melanogaster,258,rayyan-197247442,Spontaneous mutation for life-history traits in Drosophila melanogaster,1998,NA,NA,lab,female,female,NA,NA,6,6,NA,NA,NA,NA,NA,NA,line_mean_correlation,genetic_line,no,broad,authors,adult,adult,late fecundity (number of eggs),late pupal productivity (number of pupae produced),fertility,fertility,include,cor,0.54,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-197247442,table 6,fertility,fertility,genotype,0.604155603,6,1,0.604155603,female,adult,Insecta,within
889,Drosophila melanogaster,258,rayyan-197247442,Spontaneous mutation for life-history traits in Drosophila melanogaster,1998,NA,NA,lab,female,female,NA,NA,6,6,NA,NA,NA,NA,NA,NA,line_mean_correlation,genetic_line,no,broad,authors,non_adult,adult,late viability (percentage of eggs developing into pupae),late pupal productivity (number of pupae produced),survival,fertility,include,cor,0.85,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-197247442,table 6,survival,fertility,genotype,1.256152812,6,1,1.256152812,female,cross,Insecta,between
890,Drosophila melanogaster,149,rayyan-697472291,"Evolutionary responses of Drosophila melanogaster to selection at different larval densities: changes in genetic variation, specialization and phenotypic plasticity",2002,1991,"Galicia, Spain",lab,both,both,60,60,6,6,60,60,60,60,600,600,animal_model,pedigree,yes,narrow,authors,non_adult,non_adult,biomass (total pupal weight),larva-to-pupa viability,size,survival,include,cor,0.439,NA,NA,NA,NA,NA,NA,NA,NA,low,table 2,size,survival,pedigree,0.470991401,600,1,0.470991401,both,non_adult,Insecta,between
891,Drosophila melanogaster,149,rayyan-697472291,"Evolutionary responses of Drosophila melanogaster to selection at different larval densities: changes in genetic variation, specialization and phenotypic plasticity",2002,1991,"Galicia, Spain",lab,both,both,60,60,6,6,60,60,60,60,600,600,animal_model,pedigree,yes,narrow,authors,non_adult,non_adult,biomass (total pupal weight),average pupa weight ,size,size,include,cor,0.18,NA,NA,NA,NA,NA,NA,NA,NA,low,table 2,size,size,pedigree,0.181982689,600,1,0.181982689,both,non_adult,Insecta,within
892,Drosophila melanogaster,149,rayyan-697472291,"Evolutionary responses of Drosophila melanogaster to selection at different larval densities: changes in genetic variation, specialization and phenotypic plasticity",2002,1991,"Galicia, Spain",lab,both,both,60,60,6,6,60,60,60,60,600,600,animal_model,pedigree,yes,narrow,authors,non_adult,non_adult,biomass (total pupal weight),average pupation day (developmental time),size,reverse_maturation,include,cor,0.006,NA,NA,NA,NA,NA,NA,NA,NA,low,table 2,size,maturation,pedigree,0.006000072,600,-1,-0.006000072,both,non_adult,Insecta,between
893,Drosophila melanogaster,149,rayyan-697472291,"Evolutionary responses of Drosophila melanogaster to selection at different larval densities: changes in genetic variation, specialization and phenotypic plasticity",2002,1991,"Galicia, Spain",lab,both,both,60,60,6,6,60,60,60,60,600,600,animal_model,pedigree,yes,narrow,authors,non_adult,non_adult,larva-to-pupa viability,average pupa weight ,survival,size,include,cor,-0.109,NA,NA,NA,NA,NA,NA,NA,NA,low,table 2,survival,size,pedigree,-0.10943478,600,1,-0.10943478,both,non_adult,Insecta,between
894,Drosophila melanogaster,149,rayyan-697472291,"Evolutionary responses of Drosophila melanogaster to selection at different larval densities: changes in genetic variation, specialization and phenotypic plasticity",2002,1991,"Galicia, Spain",lab,both,both,60,60,6,6,60,60,60,60,600,600,animal_model,pedigree,yes,narrow,authors,non_adult,non_adult,larva-to-pupa viability,average pupation day (developmental time),survival,reverse_maturation,include,cor,-0.019,NA,NA,NA,NA,NA,NA,NA,NA,low,table 2,survival,maturation,pedigree,-0.019002287,600,-1,0.019002287,both,non_adult,Insecta,between
895,Drosophila melanogaster,149,rayyan-697472291,"Evolutionary responses of Drosophila melanogaster to selection at different larval densities: changes in genetic variation, specialization and phenotypic plasticity",2002,1991,"Galicia, Spain",lab,both,both,60,60,6,6,60,60,60,60,600,600,animal_model,pedigree,yes,narrow,authors,non_adult,non_adult,average pupa weight ,average pupation day (developmental time),size,reverse_maturation,include,cor,-0.051,NA,NA,NA,NA,NA,NA,NA,NA,low,table 2,size,maturation,pedigree,-0.051044286,600,-1,0.051044286,both,non_adult,Insecta,between
896,Drosophila melanogaster,46,rayyan-697471387,Spatially varying selection shapes life history clines among populations of Drosophila melanogaster from sub-Saharan Africa,2015,2002-2011,tropical and subtropical sub-Saharan populations,lab,female,female,NA,NA,39,39,NA,NA,NA,NA,200,233,line_mean_correlation,genetic_line,no,broad,CC,adult,both,fecundity 6-10 days (number of egg laid),lifespan of female,fertility,survival,include_2,cor,0,NA,NA,NA,NA,NA,NA,NA,NA,"above-equator (pop EF, ED, CO, EA, NG)",table s6,fertility,survival,genotype,0,39,1,0,female,cross,Insecta,between
897,Drosophila melanogaster,46,rayyan-697471387,Spatially varying selection shapes life history clines among populations of Drosophila melanogaster from sub-Saharan Africa,2015,2002-2011,tropical and subtropical sub-Saharan populations,lab,female,both,NA,NA,39,38,NA,NA,NA,NA,200,2265,line_mean_correlation,genetic_line,no,broad,CC,adult,non_adult,fecundity 6-10 days (number of egg laid),proportion egg-to-adult survival (viability),fertility,survival,include_2,cor,0.47,NA,NA,NA,NA,NA,NA,NA,NA,"above-equator (pop EF, ED, CO, EA, NG)",table s6,fertility,survival,genotype,0.510070337,38,1,0.510070337,female,cross,Insecta,between
898,Drosophila melanogaster,46,rayyan-697471387,Spatially varying selection shapes life history clines among populations of Drosophila melanogaster from sub-Saharan Africa,2015,2002-2011,tropical and subtropical sub-Saharan populations,lab,female,female,NA,NA,39,39,NA,NA,NA,NA,233,233,line_mean_correlation,genetic_line,no,broad,CC,adult,both,fecundity 1-10 days (number of eggs laid),lifespan of female,fertility,survival,include_2,cor,-0.08,NA,NA,NA,NA,NA,NA,NA,NA,"above-equator (pop EF, ED, CO, EA, NG)",table s6,fertility,survival,genotype,-0.080171325,39,1,-0.080171325,female,cross,Insecta,between
899,Drosophila melanogaster,243,rayyan-197247408,The genetic structure of female life history in D. melanogaster: Comparisons among populations,2000,NA,"Arizona, California, Ohio, USA",lab,female,female,NA,NA,NA,NA,2372,2372,345,345,NA,NA,animal_model,full/half_sib,no,narrow,authors,adult,adult,early fecundity,late fecundity,fertility,fertility,include,cor,0.51,NA,NA,NA,NA,NA,NA,NA,NA,Flagstaff_Davis_Bowling_Green_combined_sib3,table 9,fertility,fertility,family,0.562729769,2372,1,0.562729769,female,adult,Insecta,within
900,Drosophila melanogaster,153,rayyan-697472360,Age-specific patterns of genetic variance in Drosophila melanogaster .2. Fecundity and its genetic covariance with age-specific mortality,1996,1981,NA,lab,female,female,50,50,10,10,50,50,50,50,NA,NA,animal_model,genetic_line,no,narrow,authors,both,both,mortality in week 1,mortality in week 4,reverse_survival,reverse_survival,include,cor,-0.396,NA,NA,NA,NA,NA,NA,NA,NA,female,table 1,survival,survival,genotype,-0.418896043,10,1,-0.418896043,female,both,Insecta,within
901,Drosophila melanogaster,153,rayyan-697472360,Age-specific patterns of genetic variance in Drosophila melanogaster .2. Fecundity and its genetic covariance with age-specific mortality,1996,1981,NA,lab,female,female,50,50,10,10,50,50,50,50,NA,NA,animal_model,genetic_line,no,narrow,authors,both,both,mortality in week 1,mortality in week 5,reverse_survival,reverse_survival,include,cor,-0.248,NA,NA,NA,NA,NA,NA,NA,NA,female,table 1,survival,survival,genotype,-0.253280612,10,1,-0.253280612,female,both,Insecta,within
902,Drosophila melanogaster,153,rayyan-697472360,Age-specific patterns of genetic variance in Drosophila melanogaster .2. Fecundity and its genetic covariance with age-specific mortality,1996,1981,NA,lab,female,female,50,50,10,10,50,50,50,50,NA,NA,animal_model,genetic_line,no,narrow,authors,both,both,mortality in week 1,mortality in week 6,reverse_survival,reverse_survival,include,cor,0.5769,NA,NA,NA,NA,NA,NA,NA,NA,female,table 1,survival,survival,genotype,0.657803808,10,1,0.657803808,female,both,Insecta,within
903,Drosophila melanogaster,153,rayyan-697472360,Age-specific patterns of genetic variance in Drosophila melanogaster .2. Fecundity and its genetic covariance with age-specific mortality,1996,1981,NA,lab,female,female,50,50,10,10,50,50,50,50,NA,NA,animal_model,genetic_line,no,narrow,authors,both,both,mortality in week 1,mortality in week 7,reverse_survival,reverse_survival,include,cor,NA,NA,NA,NA,NA,NA,NA,NA,NA,female,table 1,survival,survival,genotype,NA,10,1,NA,female,both,Insecta,within
904,Drosophila melanogaster,153,rayyan-697472360,Age-specific patterns of genetic variance in Drosophila melanogaster .2. Fecundity and its genetic covariance with age-specific mortality,1996,1981,NA,lab,female,female,50,50,10,10,50,50,50,50,NA,NA,animal_model,genetic_line,no,narrow,authors,both,both,mortality in week 2,mortality in week 3,reverse_survival,reverse_survival,include,cor,0.7611,NA,NA,NA,NA,NA,NA,NA,NA,female,table 1,survival,survival,genotype,0.998824419,10,1,0.998824419,female,both,Insecta,within
905,Drosophila melanogaster,153,rayyan-697472360,Age-specific patterns of genetic variance in Drosophila melanogaster .2. Fecundity and its genetic covariance with age-specific mortality,1996,1981,NA,lab,female,female,50,50,10,10,50,50,50,50,NA,NA,animal_model,genetic_line,no,narrow,authors,both,both,mortality in week 2,mortality in week 4,reverse_survival,reverse_survival,include,cor,0.1143,NA,NA,NA,NA,NA,NA,NA,NA,female,table 1,survival,survival,genotype,0.114801696,10,1,0.114801696,female,both,Insecta,within
906,Drosophila melanogaster,153,rayyan-697472360,Age-specific patterns of genetic variance in Drosophila melanogaster .2. Fecundity and its genetic covariance with age-specific mortality,1996,1981,NA,lab,female,female,50,50,10,10,50,50,50,50,NA,NA,animal_model,genetic_line,no,narrow,authors,both,both,mortality in week 2,mortality in week 5,reverse_survival,reverse_survival,include,cor,0.009,NA,NA,NA,NA,NA,NA,NA,NA,female,table 1,survival,survival,genotype,0.009000243,10,1,0.009000243,female,both,Insecta,within
907,Drosophila melanogaster,153,rayyan-697472360,Age-specific patterns of genetic variance in Drosophila melanogaster .2. Fecundity and its genetic covariance with age-specific mortality,1996,1981,NA,lab,female,female,50,50,10,10,50,50,50,50,NA,NA,animal_model,genetic_line,no,narrow,authors,both,both,mortality in week 2,mortality in week 6,reverse_survival,reverse_survival,include,cor,0.0322,NA,NA,NA,NA,NA,NA,NA,NA,female,table 1,survival,survival,genotype,0.032211136,10,1,0.032211136,female,both,Insecta,within
908,Drosophila melanogaster,153,rayyan-697472360,Age-specific patterns of genetic variance in Drosophila melanogaster .2. Fecundity and its genetic covariance with age-specific mortality,1996,1981,NA,lab,female,female,50,50,10,10,50,50,50,50,NA,NA,animal_model,genetic_line,no,narrow,authors,both,both,mortality in week 2,mortality in week 7,reverse_survival,reverse_survival,include,cor,-0.554,NA,NA,NA,NA,NA,NA,NA,NA,female,table 1,survival,survival,genotype,-0.624134289,10,1,-0.624134289,female,both,Insecta,within
909,Drosophila melanogaster,153,rayyan-697472360,Age-specific patterns of genetic variance in Drosophila melanogaster .2. Fecundity and its genetic covariance with age-specific mortality,1996,1981,NA,lab,female,female,50,50,10,10,50,50,50,50,NA,NA,animal_model,genetic_line,no,narrow,authors,both,both,mortality in week 3,mortality in week 4,reverse_survival,reverse_survival,include,cor,0.857,NA,NA,NA,NA,NA,NA,NA,NA,female,table 1,survival,survival,genotype,1.281936466,10,1,1.281936466,female,both,Insecta,within
910,Drosophila melanogaster,153,rayyan-697472360,Age-specific patterns of genetic variance in Drosophila melanogaster .2. Fecundity and its genetic covariance with age-specific mortality,1996,1981,NA,lab,female,female,50,50,10,10,50,50,50,50,NA,NA,animal_model,genetic_line,no,narrow,authors,both,both,mortality in week 3,mortality in week 5,reverse_survival,reverse_survival,include,cor,0.656,NA,NA,NA,NA,NA,NA,NA,NA,female,table 1,survival,survival,genotype,0.785759339,10,1,0.785759339,female,both,Insecta,within
911,Drosophila melanogaster,153,rayyan-697472360,Age-specific patterns of genetic variance in Drosophila melanogaster .2. Fecundity and its genetic covariance with age-specific mortality,1996,1981,NA,lab,female,female,50,50,10,10,50,50,50,50,NA,NA,animal_model,genetic_line,no,narrow,authors,both,both,mortality in week 3,mortality in week 6,reverse_survival,reverse_survival,include,cor,0.582,NA,NA,NA,NA,NA,NA,NA,NA,female,table 1,survival,survival,genotype,0.665481858,10,1,0.665481858,female,both,Insecta,within
912,Drosophila melanogaster,153,rayyan-697472360,Age-specific patterns of genetic variance in Drosophila melanogaster .2. Fecundity and its genetic covariance with age-specific mortality,1996,1981,NA,lab,female,female,50,50,10,10,50,50,50,50,NA,NA,animal_model,genetic_line,no,narrow,authors,both,both,mortality in week 3,mortality in week 7,reverse_survival,reverse_survival,include,cor,0.2635,NA,NA,NA,NA,NA,NA,NA,NA,female,table 1,survival,survival,genotype,0.269865845,10,1,0.269865845,female,both,Insecta,within
913,Drosophila melanogaster,153,rayyan-697472360,Age-specific patterns of genetic variance in Drosophila melanogaster .2. Fecundity and its genetic covariance with age-specific mortality,1996,1981,NA,lab,female,female,50,50,10,10,50,50,50,50,NA,NA,animal_model,genetic_line,no,narrow,authors,both,both,mortality in week 4,mortality in week 5,reverse_survival,reverse_survival,include,cor,0.862,NA,NA,NA,NA,NA,NA,NA,NA,female,table 1,survival,survival,genotype,1.301076386,10,1,1.301076386,female,both,Insecta,within
914,Drosophila melanogaster,368,rayyan-697472840,"Life history variation in an artificially selected population of drosophila melanogaster: Pleiotropy, superflies, and age-specific adaptation",2010,NA,NA,lab,female,female,NA,NA,58,58,NA,NA,NA,NA,NA,NA,line_mean_correlation,genetic_line,yes,broad,authors,both,adult,female lifespan,daily fecundity,survival,fertility,include,cor,0.098,NA,NA,NA,NA,NA,NA,NA,NA,female_raw_all_daily_15,figure 5,survival,fertility,genotype,0.098315551,58,1,0.098315551,female,cross,Insecta,between
915,Drosophila melanogaster,368,rayyan-697472840,"Life history variation in an artificially selected population of drosophila melanogaster: Pleiotropy, superflies, and age-specific adaptation",2010,NA,NA,lab,female,female,NA,NA,58,58,NA,NA,NA,NA,NA,NA,line_mean_correlation,genetic_line,yes,broad,authors,both,adult,female lifespan,daily fecundity,survival,fertility,include,cor,0.174,NA,NA,NA,NA,NA,NA,NA,NA,female_raw_all_daily_16,figure 5,survival,fertility,genotype,0.175788613,58,1,0.175788613,female,cross,Insecta,between
916,Drosophila melanogaster,368,rayyan-697472840,"Life history variation in an artificially selected population of drosophila melanogaster: Pleiotropy, superflies, and age-specific adaptation",2010,NA,NA,lab,female,female,NA,NA,58,58,NA,NA,NA,NA,NA,NA,line_mean_correlation,genetic_line,yes,broad,authors,both,adult,female lifespan,daily fecundity,survival,fertility,include,cor,0.033,NA,NA,NA,NA,NA,NA,NA,NA,female_raw_all_daily_17,figure 5,survival,fertility,genotype,0.033011987,58,1,0.033011987,female,cross,Insecta,between
917,Drosophila melanogaster,309,rayyan-197248006,PROBING THE EVOLUTION OF SENESCENCE IN DROSOPHILA-MELANOGASTER WITH P-ELEMENT TAGGING,1995,NA,,lab,female,both,NA,NA,52,52,NA,NA,NA,NA,3419,17135,line_mean_correlation,genetic_line,no,broad,CC,adult,both,early fecundity ,longevity,fertility,survival,include,cor,0.286,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-197248006,fig 6,fertility,survival,genotype,0.294204471,52,1,0.294204471,female,cross,Insecta,between
918,Drosophila melanogaster,153,rayyan-697472360,Age-specific patterns of genetic variance in Drosophila melanogaster .2. Fecundity and its genetic covariance with age-specific mortality,1996,1981,NA,lab,female,female,50,50,10,10,50,50,50,50,NA,NA,animal_model,genetic_line,no,narrow,authors,both,both,mortality in week 6,mortality in week 7,reverse_survival,reverse_survival,include,cor,0.973,NA,NA,NA,NA,NA,NA,NA,NA,female,table 1,survival,survival,genotype,2.14573682,10,1,2.14573682,female,both,Insecta,within
919,Drosophila melanogaster,153,rayyan-697472360,Age-specific patterns of genetic variance in Drosophila melanogaster .2. Fecundity and its genetic covariance with age-specific mortality,1996,1981,NA,lab,female,female,50,50,10,10,50,50,50,50,NA,NA,animal_model,genetic_line,no,narrow,authors,adult,adult,fertility in day 3,fertility in day 7,fertility,fertility,include,cor,0.627,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-697472360,fig 3,fertility,fertility,genotype,0.736457344,10,1,0.736457344,female,adult,Insecta,within
920,Drosophila melanogaster,153,rayyan-697472360,Age-specific patterns of genetic variance in Drosophila melanogaster .2. Fecundity and its genetic covariance with age-specific mortality,1996,1981,NA,lab,female,female,50,50,10,10,50,50,50,50,NA,NA,animal_model,genetic_line,no,narrow,authors,adult,adult,fertility in day 3,fertility in day 10,fertility,fertility,include,cor,-0.359,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-697472360,fig 3,fertility,fertility,genotype,-0.375737479,10,1,-0.375737479,female,adult,Insecta,within
921,Drosophila melanogaster,153,rayyan-697472360,Age-specific patterns of genetic variance in Drosophila melanogaster .2. Fecundity and its genetic covariance with age-specific mortality,1996,1981,NA,lab,female,female,50,50,10,10,50,50,50,50,NA,NA,animal_model,genetic_line,no,narrow,authors,adult,adult,fertility in day 3,fertility in day 14,fertility,fertility,include,cor,-0.98,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-697472360,fig 3,fertility,fertility,genotype,-2.297559925,10,1,-2.297559925,female,adult,Insecta,within
922,Drosophila melanogaster,153,rayyan-697472360,Age-specific patterns of genetic variance in Drosophila melanogaster .2. Fecundity and its genetic covariance with age-specific mortality,1996,1981,NA,lab,female,female,50,50,10,10,50,50,50,50,NA,NA,animal_model,genetic_line,no,narrow,authors,adult,adult,fertility in day 3,fertility in day 17,fertility,fertility,include,cor,0.027,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-697472360,fig 3,fertility,fertility,genotype,0.027006564,10,1,0.027006564,female,adult,Insecta,within
923,Drosophila melanogaster,153,rayyan-697472360,Age-specific patterns of genetic variance in Drosophila melanogaster .2. Fecundity and its genetic covariance with age-specific mortality,1996,1981,NA,lab,female,female,50,50,10,10,50,50,50,50,NA,NA,animal_model,genetic_line,no,narrow,authors,adult,adult,fertility in day 3,fertility in day 21,fertility,fertility,include,cor,-0.146,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-697472360,fig 3,fertility,fertility,genotype,-0.147050852,10,1,-0.147050852,female,adult,Insecta,within
924,Drosophila melanogaster,153,rayyan-697472360,Age-specific patterns of genetic variance in Drosophila melanogaster .2. Fecundity and its genetic covariance with age-specific mortality,1996,1981,NA,lab,female,female,50,50,10,10,50,50,50,50,NA,NA,animal_model,genetic_line,no,narrow,authors,adult,adult,fertility in day 3,fertility in day 24,fertility,fertility,include,cor,0.075,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-697472360,fig 3,fertility,fertility,genotype,0.075141102,10,1,0.075141102,female,adult,Insecta,within
925,Drosophila melanogaster,153,rayyan-697472360,Age-specific patterns of genetic variance in Drosophila melanogaster .2. Fecundity and its genetic covariance with age-specific mortality,1996,1981,NA,lab,female,female,50,50,10,10,50,50,50,50,NA,NA,animal_model,genetic_line,no,narrow,authors,adult,adult,fertility in day 3,fertility in day 28,fertility,fertility,include,cor,0.113,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-697472360,fig 3,fertility,fertility,genotype,0.113484684,10,1,0.113484684,female,adult,Insecta,within
926,Drosophila melanogaster,153,rayyan-697472360,Age-specific patterns of genetic variance in Drosophila melanogaster .2. Fecundity and its genetic covariance with age-specific mortality,1996,1981,NA,lab,female,female,50,50,10,10,50,50,50,50,NA,NA,animal_model,genetic_line,no,narrow,authors,adult,adult,fertility in day 3,fertility in day 31,fertility,fertility,include,cor,0.062,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-697472360,fig 3,fertility,fertility,genotype,0.062079626,10,1,0.062079626,female,adult,Insecta,within
927,Drosophila melanogaster,243,rayyan-197247408,The genetic structure of female life history in D. melanogaster: Comparisons among populations,2000,NA,"Ohio, USA",lab,female,female,NA,NA,NA,NA,844,844,145,145,NA,NA,animal_model,full/half_sib,no,narrow,authors,adult,both,early fecundity,female survivorship,fertility,survival,include,cor,-0.352,NA,NA,NA,NA,NA,NA,NA,NA,Bowling_Green_sib2,table 5,fertility,survival,family,-0.36772478,844,1,-0.36772478,female,cross,Insecta,between
929,Drosophila melanogaster,243,rayyan-197247408,The genetic structure of female life history in D. melanogaster: Comparisons among populations,2000,NA,"Ohio, USA",lab,female,female,NA,NA,NA,NA,810,810,129,129,NA,NA,animal_model,full/half_sib,no,narrow,authors,non_adult,adult,development rate (reciprocal of the develoment time of the first female to eclose),late fecundity,maturation,fertility,include,cor,0.239,NA,NA,NA,NA,NA,NA,NA,NA,Bowling_Green_sib1,table 5,maturation,fertility,family,0.243713262,810,1,0.243713262,female,cross,Insecta,between
930,Drosophila melanogaster,243,rayyan-197247408,The genetic structure of female life history in D. melanogaster: Comparisons among populations,2000,NA,"Ohio, USA",lab,female,female,NA,NA,NA,NA,844,844,145,145,NA,NA,animal_model,full/half_sib,no,narrow,authors,non_adult,adult,development rate (reciprocal of the develoment time of the first female to eclose),late fecundity,maturation,fertility,include,cor,0.678,NA,NA,NA,NA,NA,NA,NA,NA,Bowling_Green_sib2,table 5,maturation,fertility,family,0.825403171,844,1,0.825403171,female,cross,Insecta,between
932,Drosophila melanogaster,243,rayyan-197247408,The genetic structure of female life history in D. melanogaster: Comparisons among populations,2000,NA,"Ohio, USA",lab,female,female,NA,NA,NA,NA,810,810,129,129,NA,NA,animal_model,full/half_sib,no,narrow,authors,non_adult,both,development rate (reciprocal of the develoment time of the first female to eclose),female survivorship,maturation,survival,include,cor,0.125,NA,NA,NA,NA,NA,NA,NA,NA,Bowling_Green_sib1,table 5,maturation,survival,family,0.125657214,810,1,0.125657214,female,cross,Insecta,between
933,Drosophila melanogaster,153,rayyan-697472360,Age-specific patterns of genetic variance in Drosophila melanogaster .2. Fecundity and its genetic covariance with age-specific mortality,1996,1981,NA,lab,female,female,50,50,10,10,50,50,50,50,NA,NA,animal_model,genetic_line,no,narrow,authors,adult,adult,fertility in day 17,fertility in day 21,fertility,fertility,include,cor,0.878,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-697472360,fig 3,fertility,fertility,genotype,1.366970808,10,1,1.366970808,female,adult,Insecta,within
934,Drosophila melanogaster,153,rayyan-697472360,Age-specific patterns of genetic variance in Drosophila melanogaster .2. Fecundity and its genetic covariance with age-specific mortality,1996,1981,NA,lab,female,female,50,50,10,10,50,50,50,50,NA,NA,animal_model,genetic_line,no,narrow,authors,adult,adult,fertility in day 17,fertility in day 24,fertility,fertility,include,cor,0.889,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-697472360,fig 3,fertility,fertility,genotype,1.417136333,10,1,1.417136333,female,adult,Insecta,within
936,Drosophila melanogaster,153,rayyan-697472360,Age-specific patterns of genetic variance in Drosophila melanogaster .2. Fecundity and its genetic covariance with age-specific mortality,1996,1981,NA,lab,female,female,50,50,10,10,50,50,50,50,NA,NA,animal_model,genetic_line,no,narrow,authors,adult,adult,fertility in day 17,fertility in day 28,fertility,fertility,include,cor,0.672,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-697472360,fig 3,fertility,fertility,genotype,0.814381093,10,1,0.814381093,female,adult,Insecta,within
937,Drosophila melanogaster,153,rayyan-697472360,Age-specific patterns of genetic variance in Drosophila melanogaster .2. Fecundity and its genetic covariance with age-specific mortality,1996,1981,NA,lab,female,female,50,50,10,10,50,50,50,50,NA,NA,animal_model,genetic_line,no,narrow,authors,adult,adult,fertility in day 17,fertility in day 31,fertility,fertility,include,cor,0.666,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-697472360,fig 3,fertility,fertility,genotype,0.803519915,10,1,0.803519915,female,adult,Insecta,within
938,Drosophila melanogaster,153,rayyan-697472360,Age-specific patterns of genetic variance in Drosophila melanogaster .2. Fecundity and its genetic covariance with age-specific mortality,1996,1981,NA,lab,female,female,50,50,10,10,50,50,50,50,NA,NA,animal_model,genetic_line,no,narrow,authors,adult,adult,fertility in day 21,fertility in day 24,fertility,fertility,include,cor,NA,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-697472360,fig 3,fertility,fertility,genotype,NA,10,1,NA,female,adult,Insecta,within
939,Drosophila melanogaster,153,rayyan-697472360,Age-specific patterns of genetic variance in Drosophila melanogaster .2. Fecundity and its genetic covariance with age-specific mortality,1996,1981,NA,lab,male,male,50,50,10,10,50,50,50,50,NA,NA,animal_model,genetic_line,no,narrow,authors,both,both,mortality in week 7,mortality in week 8,reverse_survival,reverse_survival,include,cor,0.8398,NA,NA,NA,NA,NA,NA,NA,NA,male,table 1,survival,survival,genotype,1.220494557,10,1,1.220494557,male,both,Insecta,within
940,Drosophila melanogaster,243,rayyan-197247408,The genetic structure of female life history in D. melanogaster: Comparisons among populations,2000,NA,"Arizona, California, Ohio, USA",lab,female,female,NA,NA,NA,NA,2372,2372,345,345,NA,NA,animal_model,full/half_sib,no,narrow,authors,adult,both,early fecundity,female survivorship,fertility,survival,include,cor,0.09,NA,NA,NA,NA,NA,NA,NA,NA,Flagstaff_Davis_Bowling_Green_combined_sib3,table 9,fertility,survival,family,0.090244188,2372,1,0.090244188,female,cross,Insecta,between
941,Drosophila melanogaster,153,rayyan-697472360,Age-specific patterns of genetic variance in Drosophila melanogaster .2. Fecundity and its genetic covariance with age-specific mortality,1996,1981,NA,lab,female,female,50,50,10,10,50,50,50,50,NA,NA,animal_model,genetic_line,no,narrow,authors,adult,adult,fertility in day 24,fertility in day 28,fertility,fertility,include,cor,NA,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-697472360,fig 3,fertility,fertility,genotype,NA,10,1,NA,female,adult,Insecta,within
942,Drosophila melanogaster,243,rayyan-197247408,The genetic structure of female life history in D. melanogaster: Comparisons among populations,2000,NA,"Arizona, California, Ohio, USA",lab,female,female,NA,NA,NA,NA,2372,2372,345,345,NA,NA,animal_model,full/half_sib,no,narrow,authors,non_adult,both,development rate (reciprocal of the develoment time of the first female to eclose),female survivorship,maturation,survival,include,cor,0.17,NA,NA,NA,NA,NA,NA,NA,NA,Flagstaff_Davis_Bowling_Green_combined_sib3,table 9,maturation,survival,family,0.171666664,2372,1,0.171666664,female,cross,Insecta,between
943,Drosophila melanogaster,243,rayyan-197247408,The genetic structure of female life history in D. melanogaster: Comparisons among populations,2000,NA,"Arizona, California, Ohio, USA",lab,female,female,NA,NA,NA,NA,2372,2372,345,345,NA,NA,animal_model,full/half_sib,no,narrow,authors,adult,both,late fecundity,female survivorship,fertility,survival,include,cor,0.43,NA,NA,NA,NA,NA,NA,NA,NA,Flagstaff_Davis_Bowling_Green_combined_sib3,table 9,fertility,survival,family,0.459896681,2372,1,0.459896681,female,cross,Insecta,between
944,Drosophila melanogaster,10,rayyan-178530589,Effects of temperature extremes on genetic variances for life history traits in Drosophila melanogaster as determined from parent-offspring comparisons,1998,1993,"Hstings, Australis",lab,female,both,116,116,NA,NA,116,116,116,116,166,376,family_mean_correlation,full_sib,no,broad,CC,adult,non_adult,wing length,egg-to-adult development time (days),size,reverse_maturation,include,cor,0.27,NA,NA,NA,NA,NA,NA,NA,NA,25_progeny_14_parent,table 8,size,maturation,family,0.276863823,116,-1,-0.276863823,female,cross,Insecta,between
945,Drosophila melanogaster,10,rayyan-178530589,Effects of temperature extremes on genetic variances for life history traits in Drosophila melanogaster as determined from parent-offspring comparisons,1998,1993,"Hstings, Australis",lab,female,both,96,96,NA,NA,96,96,96,96,166,376,family_mean_correlation,full_sib,no,broad,CC,adult,non_adult,wing length,egg-to-adult development time (days),size,reverse_maturation,include,cor,0.016,NA,NA,NA,NA,NA,NA,NA,NA,25_progeny_28_parent,table 8,size,maturation,family,0.016001366,96,-1,-0.016001366,female,cross,Insecta,between
946,Drosophila melanogaster,10,rayyan-178530589,Effects of temperature extremes on genetic variances for life history traits in Drosophila melanogaster as determined from parent-offspring comparisons,1998,1993,"Hstings, Australis",lab,female,both,106,106,NA,NA,106,106,106,106,166,376,family_mean_correlation,full_sib,no,broad,CC,adult,non_adult,wing length,egg-to-adult development time (days),size,reverse_maturation,include,cor,0.053,NA,NA,NA,NA,NA,NA,NA,NA,28_progeny_14_parent,table 8,size,maturation,family,0.053049709,106,-1,-0.053049709,female,cross,Insecta,between
947,Drosophila melanogaster,154,rayyan-697472367,THE EVOLUTIONARY GENETICS OF MALE LIFE-HISTORY CHARACTERS IN DROSOPHILA-MELANOGASTER,1995,1975,Amherst,lab,male,male,320,320,40,40,960,960,960,960,3017,6876,matrix,genetic_line,no,narrow,authors,adult,both,body mass,intercept of mortality,size,reverse_survival,include,cor,0.582,0.405,se,NA,NA,NA,NA,NA,NA,rayyan-697472367,table 7,size,survival,genotype,0.665481858,40,-1,-0.665481858,male,cross,Insecta,between
948,Drosophila melanogaster,10,rayyan-178530589,Effects of temperature extremes on genetic variances for life history traits in Drosophila melanogaster as determined from parent-offspring comparisons,1998,1993,"Hstings, Australis",lab,female,female,115,115,NA,NA,115,115,115,115,166,230,family_mean_correlation,full_sib,no,broad,CC,adult,adult,wing length,eggs produced in the first 10 days,size,fertility,include,cor,0.07,NA,NA,NA,NA,NA,NA,NA,NA,14_progeny_14_parent,table 8,size,fertility,family,0.070114671,115,1,0.070114671,female,adult,Insecta,between
949,Drosophila melanogaster,422,rayyan-697473383,The evolutionary costs of immunological maintenance and deployment,2008,2004,"Newfield, NY, USA",lab,female,female,NA,NA,40,40,NA,NA,NA,NA,NA,NA,line_mean_correlation,genetic_line,no,broad,CC,adult,adult,fecundity,day 9 weight,fertility,size,include,cor,0.554,NA,NA,NA,NA,NA,NA,NA,NA,unlimited,table 3,fertility,size,genotype,0.624134289,40,1,0.624134289,female,adult,Insecta,between
950,Drosophila melanogaster,10,rayyan-178530589,Effects of temperature extremes on genetic variances for life history traits in Drosophila melanogaster as determined from parent-offspring comparisons,1998,1993,"Hstings, Australis",lab,female,female,116,116,NA,NA,116,116,116,116,166,232,family_mean_correlation,full_sib,no,broad,CC,adult,adult,wing length,eggs produced in the first 10 days,size,fertility,include,cor,-0.138,NA,NA,NA,NA,NA,NA,NA,NA,25_progeny_14_parent,table 8,size,fertility,family,-0.138886172,116,1,-0.138886172,female,adult,Insecta,between
951,Drosophila melanogaster,422,rayyan-697473383,The evolutionary costs of immunological maintenance and deployment,2008,2004,"Newfield, NY, USA",lab,female,female,NA,NA,40,40,NA,NA,NA,NA,NA,NA,line_mean_correlation,genetic_line,no,broad,CC,adult,adult,fecundity,emergence weight,fertility,size,include,cor,0.168,NA,NA,NA,NA,NA,NA,NA,NA,unlimited,table 3,fertility,size,genotype,0.169607861,40,1,0.169607861,female,adult,Insecta,between
952,Drosophila melanogaster,422,rayyan-697473383,The evolutionary costs of immunological maintenance and deployment,2008,2004,"Newfield, NY, USA",lab,female,female,NA,NA,40,40,NA,NA,NA,NA,NA,NA,line_mean_correlation,genetic_line,no,broad,CC,adult,adult,fecundity,day 9 weight,fertility,size,include,cor,0.337,NA,NA,NA,NA,NA,NA,NA,NA,limited,table 3,fertility,size,genotype,0.350704293,40,1,0.350704293,female,adult,Insecta,between
953,Drosophila melanogaster,422,rayyan-697473383,The evolutionary costs of immunological maintenance and deployment,2008,2004,"Newfield, NY, USA",lab,female,female,NA,NA,40,40,NA,NA,NA,NA,NA,NA,line_mean_correlation,genetic_line,no,broad,CC,adult,adult,fecundity,weight gain (day 9 weight minus emergence weight),fertility,growth,include,cor,0.189,NA,NA,NA,NA,NA,NA,NA,NA,limited,table 3,fertility,growth,genotype,0.191299921,40,1,0.191299921,female,adult,Insecta,between
954,Drosophila melanogaster,422,rayyan-697473383,The evolutionary costs of immunological maintenance and deployment,2008,2004,"Newfield, NY, USA",lab,female,female,NA,NA,40,40,NA,NA,NA,NA,NA,NA,line_mean_correlation,genetic_line,no,broad,CC,adult,adult,fecundity,emergence weight,fertility,size,include,cor,0.171,NA,NA,NA,NA,NA,NA,NA,NA,limited,table 3,fertility,size,genotype,0.172696604,40,1,0.172696604,female,adult,Insecta,between
957,Drosophila melanogaster,154,rayyan-697472367,THE EVOLUTIONARY GENETICS OF MALE LIFE-HISTORY CHARACTERS IN DROSOPHILA-MELANOGASTER,1995,1975,Amherst,lab,male,male,320,320,40,40,960,960,960,960,6876,6876,matrix,genetic_line,no,narrow,authors,both,both,intercept of mortality,mean longevity ,reverse_survival,survival,include,cor,-0.404,0.276,se,NA,NA,NA,NA,NA,NA,rayyan-697472367,table 7,survival,survival,genotype,-0.428419959,40,-1,0.428419959,male,both,Insecta,within
958,Drosophila melanogaster,153,rayyan-697472360,Age-specific patterns of genetic variance in Drosophila melanogaster .2. Fecundity and its genetic covariance with age-specific mortality,1996,1981,NA,lab,male,male,50,50,10,10,50,50,50,50,NA,NA,animal_model,genetic_line,no,narrow,authors,both,both,mortality in week 2,mortality in week 3,reverse_survival,reverse_survival,include,cor,0.861,NA,NA,NA,NA,NA,NA,NA,NA,male,table 1,survival,survival,genotype,1.297197662,10,1,1.297197662,male,both,Insecta,within
959,Drosophila melanogaster,125,rayyan-697471866,Effects on fitness components of P-element inserts in Drosophila melanogaster: Analysis of trade-offs,1996,NA,NA,lab,both,both,NA,NA,12,12,NA,NA,NA,NA,720,720,line_mean_correlation,genetic_line,no,broad,CC,adult,adult,birth rate in the first five days after eclosion,birth rate in the 25-30 days after eclosion,fertility,fertility,include,cor,-0.5625,NA,NA,NA,NA,NA,NA,NA,NA,25,figure 5a,fertility,fertility,genotype,-0.636482838,12,1,-0.636482838,both,adult,Insecta,within
960,Drosophila melanogaster,125,rayyan-697471866,Effects on fitness components of P-element inserts in Drosophila melanogaster: Analysis of trade-offs,1996,NA,NA,lab,both,both,NA,NA,12,12,NA,NA,NA,NA,720,720,line_mean_correlation,genetic_line,no,broad,CC,adult,adult,birth rate in the first five days after eclosion,birth rate in the 30-35 days after eclosion,fertility,fertility,include,cor,-0.463541667,NA,NA,NA,NA,NA,NA,NA,NA,25,figure 5a,fertility,fertility,genotype,-0.501812841,12,1,-0.501812841,both,adult,Insecta,within
961,Drosophila melanogaster,125,rayyan-697471866,Effects on fitness components of P-element inserts in Drosophila melanogaster: Analysis of trade-offs,1996,NA,NA,lab,both,both,NA,NA,12,12,NA,NA,NA,NA,720,720,line_mean_correlation,genetic_line,no,broad,CC,adult,adult,birth rate in the first five days after eclosion,birth rate in the 35-40 days after eclosion,fertility,fertility,include,cor,0.098958333,NA,NA,NA,NA,NA,NA,NA,NA,25,figure 5a,fertility,fertility,genotype,0.099283269,12,1,0.099283269,both,adult,Insecta,within
962,Drosophila melanogaster,125,rayyan-697471866,Effects on fitness components of P-element inserts in Drosophila melanogaster: Analysis of trade-offs,1996,NA,NA,lab,both,both,NA,NA,12,12,NA,NA,NA,NA,720,720,line_mean_correlation,genetic_line,no,broad,CC,adult,adult,birth rate in the first five days after eclosion,birth rate in the 40-45 days after eclosion,fertility,fertility,include,cor,-0.3125,NA,NA,NA,NA,NA,NA,NA,NA,25,figure 5a,fertility,fertility,genotype,-0.323313582,12,1,-0.323313582,both,adult,Insecta,within
963,Drosophila melanogaster,125,rayyan-697471866,Effects on fitness components of P-element inserts in Drosophila melanogaster: Analysis of trade-offs,1996,NA,NA,lab,both,both,NA,NA,12,12,NA,NA,NA,NA,720,720,line_mean_correlation,genetic_line,no,broad,CC,adult,adult,birth rate in the first five days after eclosion,birth rate in the 5-10 days after eclosion,fertility,fertility,include,cor,0.989583333,NA,NA,NA,NA,NA,NA,NA,NA,29,figure 5a,fertility,fertility,genotype,2.626136698,12,1,2.626136698,both,adult,Insecta,within
964,Drosophila melanogaster,125,rayyan-697471866,Effects on fitness components of P-element inserts in Drosophila melanogaster: Analysis of trade-offs,1996,NA,NA,lab,both,both,NA,NA,12,12,NA,NA,NA,NA,720,720,line_mean_correlation,genetic_line,no,broad,CC,adult,adult,birth rate in the first five days after eclosion,birth rate in the 10-15 days after eclosion,fertility,fertility,include,cor,0.140625,NA,NA,NA,NA,NA,NA,NA,NA,29,figure 5a,fertility,fertility,genotype,0.141563128,12,1,0.141563128,both,adult,Insecta,within
965,Drosophila melanogaster,125,rayyan-697471866,Effects on fitness components of P-element inserts in Drosophila melanogaster: Analysis of trade-offs,1996,NA,NA,lab,both,both,NA,NA,12,12,NA,NA,NA,NA,720,720,line_mean_correlation,genetic_line,no,broad,CC,adult,adult,birth rate in the first five days after eclosion,birth rate in the 15-20 days after eclosion,fertility,fertility,include,cor,-0.177083333,NA,NA,NA,NA,NA,NA,NA,NA,29,figure 5a,fertility,fertility,genotype,-0.178969983,12,1,-0.178969983,both,adult,Insecta,within
966,Drosophila melanogaster,125,rayyan-697471866,Effects on fitness components of P-element inserts in Drosophila melanogaster: Analysis of trade-offs,1996,NA,NA,lab,both,both,NA,NA,12,12,NA,NA,NA,NA,720,720,line_mean_correlation,genetic_line,no,broad,CC,adult,adult,birth rate in the first five days after eclosion,birth rate in the 20-25 days after eclosion,fertility,fertility,include,cor,0.359375,NA,NA,NA,NA,NA,NA,NA,NA,29,figure 5a,fertility,fertility,genotype,0.376168026,12,1,0.376168026,both,adult,Insecta,within
967,Drosophila melanogaster,125,rayyan-697471866,Effects on fitness components of P-element inserts in Drosophila melanogaster: Analysis of trade-offs,1996,NA,NA,lab,both,both,NA,NA,12,12,NA,NA,NA,NA,720,720,line_mean_correlation,genetic_line,no,broad,CC,adult,adult,birth rate in the first five days after eclosion,birth rate in the 25-30 days after eclosion,fertility,fertility,include,cor,0.598958333,NA,NA,NA,NA,NA,NA,NA,NA,29,figure 5a,fertility,fertility,genotype,0.691521162,12,1,0.691521162,both,adult,Insecta,within
968,Drosophila melanogaster,125,rayyan-697471866,Effects on fitness components of P-element inserts in Drosophila melanogaster: Analysis of trade-offs,1996,NA,NA,lab,both,both,NA,NA,12,12,NA,NA,NA,NA,720,720,line_mean_correlation,genetic_line,no,broad,CC,adult,adult,birth rate in the first five days after eclosion,birth rate in the 30-35 days after eclosion,fertility,fertility,include,cor,0.489583333,NA,NA,NA,NA,NA,NA,NA,NA,29,figure 5a,fertility,fertility,genotype,0.535512166,12,1,0.535512166,both,adult,Insecta,within
969,Drosophila melanogaster,125,rayyan-697471866,Effects on fitness components of P-element inserts in Drosophila melanogaster: Analysis of trade-offs,1996,NA,NA,lab,both,both,NA,NA,12,12,NA,NA,NA,NA,720,7200,line_mean_correlation,genetic_line,no,broad,CC,adult,both,birth rate in the first five days after eclosion,mortality in the 0-5 days,fertility,reverse_survival,include,cor,-0.460732984,NA,NA,NA,NA,NA,NA,NA,NA,25,figure 5b,fertility,survival,genotype,-0.498241396,12,-1,0.498241396,both,cross,Insecta,between
970,Drosophila melanogaster,125,rayyan-697471866,Effects on fitness components of P-element inserts in Drosophila melanogaster: Analysis of trade-offs,1996,NA,NA,lab,both,both,NA,NA,12,12,NA,NA,NA,NA,720,7200,line_mean_correlation,genetic_line,no,broad,CC,adult,both,birth rate in the first five days after eclosion,mortality in the 5-10 days,fertility,reverse_survival,include,cor,-0.293193717,NA,NA,NA,NA,NA,NA,NA,NA,25,figure 5b,fertility,survival,genotype,-0.302056779,12,-1,0.302056779,both,cross,Insecta,between
971,Drosophila melanogaster,125,rayyan-697471866,Effects on fitness components of P-element inserts in Drosophila melanogaster: Analysis of trade-offs,1996,NA,NA,lab,both,both,NA,NA,12,12,NA,NA,NA,NA,720,7200,line_mean_correlation,genetic_line,no,broad,CC,adult,both,birth rate in the first five days after eclosion,mortality in the 10-15 days,fertility,reverse_survival,include,cor,0.884816754,NA,NA,NA,NA,NA,NA,NA,NA,25,figure 5b,fertility,survival,genotype,1.397530789,12,-1,-1.397530789,both,cross,Insecta,between
972,Drosophila melanogaster,125,rayyan-697471866,Effects on fitness components of P-element inserts in Drosophila melanogaster: Analysis of trade-offs,1996,NA,NA,lab,both,both,NA,NA,12,12,NA,NA,NA,NA,720,7200,line_mean_correlation,genetic_line,no,broad,CC,adult,both,birth rate in the first five days after eclosion,mortality in the 15-20 days,fertility,reverse_survival,include,cor,0.848167539,NA,NA,NA,NA,NA,NA,NA,NA,25,figure 5b,fertility,survival,genotype,1.249586113,12,-1,-1.249586113,both,cross,Insecta,between
973,Drosophila melanogaster,125,rayyan-697471866,Effects on fitness components of P-element inserts in Drosophila melanogaster: Analysis of trade-offs,1996,NA,NA,lab,both,both,NA,NA,12,12,NA,NA,NA,NA,720,7200,line_mean_correlation,genetic_line,no,broad,CC,adult,both,birth rate in the first five days after eclosion,mortality in the 20-25 days,fertility,reverse_survival,include,cor,0.560209424,NA,NA,NA,NA,NA,NA,NA,NA,25,figure 5b,fertility,survival,genotype,0.633138344,12,-1,-0.633138344,both,cross,Insecta,between
974,Drosophila melanogaster,125,rayyan-697471866,Effects on fitness components of P-element inserts in Drosophila melanogaster: Analysis of trade-offs,1996,NA,NA,lab,both,both,NA,NA,12,12,NA,NA,NA,NA,720,7200,line_mean_correlation,genetic_line,no,broad,CC,adult,both,birth rate in the first five days after eclosion,mortality in the 25-30 days,fertility,reverse_survival,include,cor,0.518324607,NA,NA,NA,NA,NA,NA,NA,NA,25,figure 5b,fertility,survival,genotype,0.574046173,12,-1,-0.574046173,both,cross,Insecta,between
975,Drosophila melanogaster,125,rayyan-697471866,Effects on fitness components of P-element inserts in Drosophila melanogaster: Analysis of trade-offs,1996,NA,NA,lab,both,both,NA,NA,12,12,NA,NA,NA,NA,720,7200,line_mean_correlation,genetic_line,no,broad,CC,adult,both,birth rate in the first five days after eclosion,mortality in the 30-35 days,fertility,reverse_survival,include,cor,0.560209424,NA,NA,NA,NA,NA,NA,NA,NA,25,figure 5b,fertility,survival,genotype,0.633138344,12,-1,-0.633138344,both,cross,Insecta,between
976,Drosophila melanogaster,125,rayyan-697471866,Effects on fitness components of P-element inserts in Drosophila melanogaster: Analysis of trade-offs,1996,NA,NA,lab,both,both,NA,NA,12,12,NA,NA,NA,NA,720,7200,line_mean_correlation,genetic_line,no,broad,CC,adult,both,birth rate in the first five days after eclosion,mortality in the 35-40 days,fertility,reverse_survival,include,cor,0.141361257,NA,NA,NA,NA,NA,NA,NA,NA,25,figure 5b,fertility,survival,genotype,0.142314318,12,-1,-0.142314318,both,cross,Insecta,between
977,Drosophila melanogaster,125,rayyan-697471866,Effects on fitness components of P-element inserts in Drosophila melanogaster: Analysis of trade-offs,1996,NA,NA,lab,both,both,NA,NA,12,12,NA,NA,NA,NA,720,7200,line_mean_correlation,genetic_line,no,broad,CC,adult,both,birth rate in the first five days after eclosion,mortality in the 40-45 days,fertility,reverse_survival,include,cor,0.989528796,NA,NA,NA,NA,NA,NA,NA,NA,25,figure 5b,fertility,survival,genotype,2.623512045,12,-1,-2.623512045,both,cross,Insecta,between
978,Drosophila melanogaster,153,rayyan-697472360,Age-specific patterns of genetic variance in Drosophila melanogaster .2. Fecundity and its genetic covariance with age-specific mortality,1996,1981,NA,lab,male,male,50,50,10,10,50,50,50,50,NA,NA,animal_model,genetic_line,no,narrow,authors,both,both,mortality in week 6,mortality in week 8,reverse_survival,reverse_survival,include,cor,0.3967,NA,NA,NA,NA,NA,NA,NA,NA,male,table 1,survival,survival,genotype,0.419726502,10,1,0.419726502,male,both,Insecta,within
980,Drosophila melanogaster,153,rayyan-697472360,Age-specific patterns of genetic variance in Drosophila melanogaster .2. Fecundity and its genetic covariance with age-specific mortality,1996,1981,NA,lab,female,female,50,50,10,10,50,50,50,50,NA,NA,animal_model,genetic_line,no,narrow,authors,both,both,mortality in week 1,mortality in week 2,reverse_survival,reverse_survival,include,cor,0.68,NA,NA,NA,NA,NA,NA,NA,NA,female,table 1,survival,survival,genotype,0.829114038,10,1,0.829114038,female,both,Insecta,within
981,Drosophila melanogaster,153,rayyan-697472360,Age-specific patterns of genetic variance in Drosophila melanogaster .2. Fecundity and its genetic covariance with age-specific mortality,1996,1981,NA,lab,female,female,50,50,10,10,50,50,50,50,NA,NA,animal_model,genetic_line,no,narrow,authors,both,both,mortality in week 1,mortality in week 3,reverse_survival,reverse_survival,include,cor,0.228,NA,NA,NA,NA,NA,NA,NA,NA,female,table 1,survival,survival,genotype,0.232078779,10,1,0.232078779,female,both,Insecta,within
982,Drosophila melanogaster,10,rayyan-178530589,Effects of temperature extremes on genetic variances for life history traits in Drosophila melanogaster as determined from parent-offspring comparisons,1998,1993,"Hstings, Australis",lab,female,both,115,115,NA,NA,115,115,115,115,166,374,family_mean_correlation,full_sib,no,broad,CC,adult,non_adult,wing length,egg-to-adult development time (days),size,reverse_maturation,include,cor,0.003,NA,NA,NA,NA,NA,NA,NA,NA,14_progeny_14_parent,table 8,size,maturation,family,0.003000009,115,-1,-0.003000009,female,cross,Insecta,between
983,Drosophila melanogaster,10,rayyan-178530589,Effects of temperature extremes on genetic variances for life history traits in Drosophila melanogaster as determined from parent-offspring comparisons,1998,1993,"Hstings, Australis",lab,female,both,98,98,NA,NA,98,98,98,98,166,376,family_mean_correlation,full_sib,no,broad,CC,adult,non_adult,wing length,egg-to-adult development time (days),size,reverse_maturation,include,cor,-0.171,NA,NA,NA,NA,NA,NA,NA,NA,14_progeny_28_parent,table 8,size,maturation,family,-0.172696604,98,-1,0.172696604,female,cross,Insecta,between
985,Drosophila melanogaster,243,rayyan-197247408,The genetic structure of female life history in D. melanogaster: Comparisons among populations,2000,NA,"California, USA",lab,female,female,NA,NA,NA,NA,663,663,126,126,NA,NA,animal_model,full/half_sib,no,narrow,authors,adult,non_adult,early fecundity,development rate (reciprocal of the develoment time of the first female to eclose),fertility,maturation,include,cor,-0.279,NA,NA,NA,NA,NA,NA,NA,NA,Davis_sib1,table 5,fertility,maturation,family,-0.286597332,663,1,-0.286597332,female,cross,Insecta,between
986,Drosophila melanogaster,243,rayyan-197247408,The genetic structure of female life history in D. melanogaster: Comparisons among populations,2000,NA,"California, USA",lab,female,female,NA,NA,NA,NA,786,786,154,154,NA,NA,animal_model,full/half_sib,no,narrow,authors,adult,non_adult,early fecundity,development rate (reciprocal of the develoment time of the first female to eclose),fertility,maturation,include,cor,0.843,NA,NA,NA,NA,NA,NA,NA,NA,Davis_sib2,table 5,fertility,maturation,family,1.231452076,786,1,1.231452076,female,cross,Insecta,between
987,Drosophila melanogaster,10,rayyan-178530589,Effects of temperature extremes on genetic variances for life history traits in Drosophila melanogaster as determined from parent-offspring comparisons,1998,1993,"Hstings, Australis",lab,female,both,94,94,NA,NA,94,94,94,94,166,376,family_mean_correlation,full_sib,no,broad,CC,adult,non_adult,wing length,egg-to-adult development time (days),size,reverse_maturation,include,cor,0.157,NA,NA,NA,NA,NA,NA,NA,NA,28_progeny_28_parent,table 8,size,maturation,family,0.158309385,94,-1,-0.158309385,female,cross,Insecta,between
988,Drosophila melanogaster,243,rayyan-197247408,The genetic structure of female life history in D. melanogaster: Comparisons among populations,2000,NA,"California, USA",lab,female,female,NA,NA,NA,NA,663,663,126,126,NA,NA,animal_model,full/half_sib,no,narrow,authors,adult,adult,early fecundity,late fecundity,fertility,fertility,include,cor,0.123,NA,NA,NA,NA,NA,NA,NA,NA,Davis_sib1,table 5,fertility,fertility,family,0.123625981,663,1,0.123625981,female,adult,Insecta,within
989,Drosophila melanogaster,10,rayyan-178530589,Effects of temperature extremes on genetic variances for life history traits in Drosophila melanogaster as determined from parent-offspring comparisons,1998,1993,"Hstings, Australis",lab,female,female,98,98,NA,NA,98,98,98,98,166,196,family_mean_correlation,full_sib,no,broad,CC,adult,adult,wing length,eggs produced in the first 10 days,size,fertility,include,cor,0.097,NA,NA,NA,NA,NA,NA,NA,NA,14_progeny_28_parent,table 8,size,fertility,family,0.097305953,98,1,0.097305953,female,adult,Insecta,between
991,Drosophila melanogaster,10,rayyan-178530589,Effects of temperature extremes on genetic variances for life history traits in Drosophila melanogaster as determined from parent-offspring comparisons,1998,1993,"Hstings, Australis",lab,female,female,96,96,NA,NA,96,96,96,96,166,192,family_mean_correlation,full_sib,no,broad,CC,adult,adult,wing length,eggs produced in the first 10 days,size,fertility,include,cor,0.085,NA,NA,NA,NA,NA,NA,NA,NA,25_progeny_28_parent,table 8,size,fertility,family,0.0852056,96,1,0.0852056,female,adult,Insecta,between
992,Drosophila melanogaster,10,rayyan-178530589,Effects of temperature extremes on genetic variances for life history traits in Drosophila melanogaster as determined from parent-offspring comparisons,1998,1993,"Hstings, Australis",lab,female,female,106,106,NA,NA,106,106,106,106,166,212,family_mean_correlation,full_sib,no,broad,CC,adult,adult,wing length,eggs produced in the first 10 days,size,fertility,include,cor,0.2,NA,NA,NA,NA,NA,NA,NA,NA,28_progeny_14_parent,table 8,size,fertility,family,0.202732554,106,1,0.202732554,female,adult,Insecta,between
993,Drosophila melanogaster,10,rayyan-178530589,Effects of temperature extremes on genetic variances for life history traits in Drosophila melanogaster as determined from parent-offspring comparisons,1998,1993,"Hstings, Australis",lab,female,female,94,94,NA,NA,94,94,94,94,166,188,family_mean_correlation,full_sib,no,broad,CC,adult,adult,wing length,eggs produced in the first 10 days,size,fertility,include,cor,-0.005,NA,NA,NA,NA,NA,NA,NA,NA,28_progeny_28_parent,table 8,size,fertility,family,-0.005000042,94,1,-0.005000042,female,adult,Insecta,between
994,Drosophila melanogaster,10,rayyan-178530589,Effects of temperature extremes on genetic variances for life history traits in Drosophila melanogaster as determined from parent-offspring comparisons,1998,1993,"Hstings, Australis",lab,both,female,115,115,NA,NA,115,115,115,115,376,230,family_mean_correlation,full_sib,no,broad,CC,non_adult,adult,egg-to-adult development time (days),eggs produced in the first 10 days,reverse_maturation,fertility,include,cor,-0.235,NA,NA,NA,NA,NA,NA,NA,NA,14_progeny_14_parent,table 8,maturation,fertility,family,-0.239475208,115,-1,0.239475208,female,cross,Insecta,between
995,Drosophila melanogaster,422,rayyan-697473383,The evolutionary costs of immunological maintenance and deployment,2008,2004,"Newfield, NY, USA",lab,female,female,NA,NA,40,40,NA,NA,NA,NA,NA,NA,line_mean_correlation,genetic_line,no,broad,CC,adult,adult,day 9 weight,weight gain (day 9 weight minus emergence weight),size,growth,include,cor,0.721,NA,NA,NA,NA,NA,NA,NA,NA,unlimited,table 3,size,growth,genotype,0.909724507,40,1,0.909724507,female,adult,Insecta,between
996,Drosophila melanogaster,422,rayyan-697473383,The evolutionary costs of immunological maintenance and deployment,2008,2004,"Newfield, NY, USA",lab,female,female,NA,NA,40,40,NA,NA,NA,NA,NA,NA,line_mean_correlation,genetic_line,no,broad,CC,adult,adult,day 9 weight,emergence weight,size,size,include,cor,0.318,NA,NA,NA,NA,NA,NA,NA,NA,unlimited,table 3,size,size,genotype,0.329420529,40,1,0.329420529,female,adult,Insecta,within
997,Drosophila melanogaster,153,rayyan-697472360,Age-specific patterns of genetic variance in Drosophila melanogaster .2. Fecundity and its genetic covariance with age-specific mortality,1996,1981,NA,lab,male,male,50,50,10,10,50,50,50,50,NA,NA,animal_model,genetic_line,no,narrow,authors,both,both,mortality in week 1,mortality in week 8,reverse_survival,reverse_survival,include,cor,0.898,NA,NA,NA,NA,NA,NA,NA,NA,male,table 1,survival,survival,genotype,1.461791583,10,1,1.461791583,male,both,Insecta,within
998,Drosophila melanogaster,153,rayyan-697472360,Age-specific patterns of genetic variance in Drosophila melanogaster .2. Fecundity and its genetic covariance with age-specific mortality,1996,1981,NA,lab,female,female,50,50,10,10,50,50,50,50,NA,NA,animal_model,genetic_line,no,narrow,authors,both,both,mortality in week 5,mortality in week 7,reverse_survival,reverse_survival,include,cor,0.866,NA,NA,NA,NA,NA,NA,NA,NA,female,table 1,survival,survival,genotype,1.316856291,10,1,1.316856291,female,both,Insecta,within
999,Drosophila melanogaster,153,rayyan-697472360,Age-specific patterns of genetic variance in Drosophila melanogaster .2. Fecundity and its genetic covariance with age-specific mortality,1996,1981,NA,lab,male,male,50,50,10,10,50,50,50,50,NA,NA,animal_model,genetic_line,no,narrow,authors,both,both,mortality in week 2,mortality in week 4,reverse_survival,reverse_survival,include,cor,NA,NA,NA,NA,NA,NA,NA,NA,NA,male,table 1,survival,survival,genotype,NA,10,1,NA,male,both,Insecta,within
1000,Drosophila melanogaster,153,rayyan-697472360,Age-specific patterns of genetic variance in Drosophila melanogaster .2. Fecundity and its genetic covariance with age-specific mortality,1996,1981,NA,lab,male,male,50,50,10,10,50,50,50,50,NA,NA,animal_model,genetic_line,no,narrow,authors,both,both,mortality in week 2,mortality in week 5,reverse_survival,reverse_survival,include,cor,0.838,NA,NA,NA,NA,NA,NA,NA,NA,male,table 1,survival,survival,genotype,1.214418484,10,1,1.214418484,male,both,Insecta,within
1001,Drosophila melanogaster,153,rayyan-697472360,Age-specific patterns of genetic variance in Drosophila melanogaster .2. Fecundity and its genetic covariance with age-specific mortality,1996,1981,NA,lab,male,male,50,50,10,10,50,50,50,50,NA,NA,animal_model,genetic_line,no,narrow,authors,both,both,mortality in week 2,mortality in week 6,reverse_survival,reverse_survival,include,cor,0.808,NA,NA,NA,NA,NA,NA,NA,NA,male,table 1,survival,survival,genotype,1.121240584,10,1,1.121240584,male,both,Insecta,within
1002,Drosophila melanogaster,153,rayyan-697472360,Age-specific patterns of genetic variance in Drosophila melanogaster .2. Fecundity and its genetic covariance with age-specific mortality,1996,1981,NA,lab,male,male,50,50,10,10,50,50,50,50,NA,NA,animal_model,genetic_line,no,narrow,authors,both,both,mortality in week 2,mortality in week 7,reverse_survival,reverse_survival,include,cor,0.838,NA,NA,NA,NA,NA,NA,NA,NA,male,table 1,survival,survival,genotype,1.214418484,10,1,1.214418484,male,both,Insecta,within
1003,Drosophila melanogaster,153,rayyan-697472360,Age-specific patterns of genetic variance in Drosophila melanogaster .2. Fecundity and its genetic covariance with age-specific mortality,1996,1981,NA,lab,male,male,50,50,10,10,50,50,50,50,NA,NA,animal_model,genetic_line,no,narrow,authors,both,both,mortality in week 2,mortality in week 8,reverse_survival,reverse_survival,include,cor,0.3642,NA,NA,NA,NA,NA,NA,NA,NA,male,table 1,survival,survival,genotype,0.381719703,10,1,0.381719703,male,both,Insecta,within
1004,Drosophila melanogaster,153,rayyan-697472360,Age-specific patterns of genetic variance in Drosophila melanogaster .2. Fecundity and its genetic covariance with age-specific mortality,1996,1981,NA,lab,male,male,50,50,10,10,50,50,50,50,NA,NA,animal_model,genetic_line,no,narrow,authors,both,both,mortality in week 3,mortality in week 4,reverse_survival,reverse_survival,include,cor,0.5815,NA,NA,NA,NA,NA,NA,NA,NA,male,table 1,survival,survival,genotype,0.664726076,10,1,0.664726076,male,both,Insecta,within
1005,Drosophila melanogaster,153,rayyan-697472360,Age-specific patterns of genetic variance in Drosophila melanogaster .2. Fecundity and its genetic covariance with age-specific mortality,1996,1981,NA,lab,male,male,50,50,10,10,50,50,50,50,NA,NA,animal_model,genetic_line,no,narrow,authors,both,both,mortality in week 3,mortality in week 5,reverse_survival,reverse_survival,include,cor,0.4244,NA,NA,NA,NA,NA,NA,NA,NA,male,table 1,survival,survival,genotype,0.453046488,10,1,0.453046488,male,both,Insecta,within
1006,Drosophila melanogaster,153,rayyan-697472360,Age-specific patterns of genetic variance in Drosophila melanogaster .2. Fecundity and its genetic covariance with age-specific mortality,1996,1981,NA,lab,male,male,50,50,10,10,50,50,50,50,NA,NA,animal_model,genetic_line,no,narrow,authors,both,both,mortality in week 3,mortality in week 6,reverse_survival,reverse_survival,include,cor,0.1914,NA,NA,NA,NA,NA,NA,NA,NA,male,table 1,survival,survival,genotype,0.193790004,10,1,0.193790004,male,both,Insecta,within
1007,Drosophila melanogaster,153,rayyan-697472360,Age-specific patterns of genetic variance in Drosophila melanogaster .2. Fecundity and its genetic covariance with age-specific mortality,1996,1981,NA,lab,male,male,50,50,10,10,50,50,50,50,NA,NA,animal_model,genetic_line,no,narrow,authors,both,both,mortality in week 3,mortality in week 7,reverse_survival,reverse_survival,include,cor,0.0943,NA,NA,NA,NA,NA,NA,NA,NA,male,table 1,survival,survival,genotype,0.094581022,10,1,0.094581022,male,both,Insecta,within
1008,Drosophila melanogaster,153,rayyan-697472360,Age-specific patterns of genetic variance in Drosophila melanogaster .2. Fecundity and its genetic covariance with age-specific mortality,1996,1981,NA,lab,male,male,50,50,10,10,50,50,50,50,NA,NA,animal_model,genetic_line,no,narrow,authors,both,both,mortality in week 3,mortality in week 8,reverse_survival,reverse_survival,include,cor,-0.27,NA,NA,NA,NA,NA,NA,NA,NA,male,table 1,survival,survival,genotype,-0.276863823,10,1,-0.276863823,male,both,Insecta,within
1009,Drosophila melanogaster,153,rayyan-697472360,Age-specific patterns of genetic variance in Drosophila melanogaster .2. Fecundity and its genetic covariance with age-specific mortality,1996,1981,NA,lab,male,male,50,50,10,10,50,50,50,50,NA,NA,animal_model,genetic_line,no,narrow,authors,both,both,mortality in week 4,mortality in week 5,reverse_survival,reverse_survival,include,cor,0.941,NA,NA,NA,NA,NA,NA,NA,NA,male,table 1,survival,survival,genotype,1.74671057,10,1,1.74671057,male,both,Insecta,within
1010,Drosophila melanogaster,153,rayyan-697472360,Age-specific patterns of genetic variance in Drosophila melanogaster .2. Fecundity and its genetic covariance with age-specific mortality,1996,1981,NA,lab,male,male,50,50,10,10,50,50,50,50,NA,NA,animal_model,genetic_line,no,narrow,authors,both,both,mortality in week 4,mortality in week 6,reverse_survival,reverse_survival,include,cor,0.825,NA,NA,NA,NA,NA,NA,NA,NA,male,table 1,survival,survival,genotype,1.172274646,10,1,1.172274646,male,both,Insecta,within
1011,Drosophila melanogaster,153,rayyan-697472360,Age-specific patterns of genetic variance in Drosophila melanogaster .2. Fecundity and its genetic covariance with age-specific mortality,1996,1981,NA,lab,male,male,50,50,10,10,50,50,50,50,NA,NA,animal_model,genetic_line,no,narrow,authors,both,both,mortality in week 4,mortality in week 7,reverse_survival,reverse_survival,include,cor,0.791,NA,NA,NA,NA,NA,NA,NA,NA,male,table 1,survival,survival,genotype,1.074097575,10,1,1.074097575,male,both,Insecta,within
1012,Drosophila melanogaster,153,rayyan-697472360,Age-specific patterns of genetic variance in Drosophila melanogaster .2. Fecundity and its genetic covariance with age-specific mortality,1996,1981,NA,lab,male,male,50,50,10,10,50,50,50,50,NA,NA,animal_model,genetic_line,no,narrow,authors,both,both,mortality in week 4,mortality in week 8,reverse_survival,reverse_survival,include,cor,0.1897,NA,NA,NA,NA,NA,NA,NA,NA,male,table 1,survival,survival,genotype,0.192025952,10,1,0.192025952,male,both,Insecta,within
1013,Drosophila melanogaster,153,rayyan-697472360,Age-specific patterns of genetic variance in Drosophila melanogaster .2. Fecundity and its genetic covariance with age-specific mortality,1996,1981,NA,lab,male,male,50,50,10,10,50,50,50,50,NA,NA,animal_model,genetic_line,no,narrow,authors,both,both,mortality in week 5,mortality in week 6,reverse_survival,reverse_survival,include,cor,0.969,NA,NA,NA,NA,NA,NA,NA,NA,male,table 1,survival,survival,genotype,2.075646937,10,1,2.075646937,male,both,Insecta,within
1014,Drosophila melanogaster,153,rayyan-697472360,Age-specific patterns of genetic variance in Drosophila melanogaster .2. Fecundity and its genetic covariance with age-specific mortality,1996,1981,NA,lab,male,male,50,50,10,10,50,50,50,50,NA,NA,animal_model,genetic_line,no,narrow,authors,both,both,mortality in week 5,mortality in week 7,reverse_survival,reverse_survival,include,cor,0.904,NA,NA,NA,NA,NA,NA,NA,NA,male,table 1,survival,survival,genotype,1.493682012,10,1,1.493682012,male,both,Insecta,within
1015,Drosophila melanogaster,46,rayyan-697471387,Spatially varying selection shapes life history clines among populations of Drosophila melanogaster from sub-Saharan Africa,2015,2002-2011,tropical and subtropical sub-Saharan populations,lab,female,both,NA,NA,39,38,NA,NA,NA,NA,230,2265,line_mean_correlation,genetic_line,no,broad,CC,adult,non_adult,fecundity 1-5 days (number of egg laid),proportion egg-to-adult survival (viability),fertility,survival,include_2,cor,0.27,NA,NA,NA,NA,NA,NA,NA,NA,"above-equator (pop EF, ED, CO, EA, NG)",table s6,fertility,survival,genotype,0.276863823,38,1,0.276863823,female,cross,Insecta,between
1016,Drosophila melanogaster,46,rayyan-697471387,Spatially varying selection shapes life history clines among populations of Drosophila melanogaster from sub-Saharan Africa,2015,2002-2011,tropical and subtropical sub-Saharan populations,lab,female,female,NA,NA,39,39,NA,NA,NA,NA,200,200,line_mean_correlation,genetic_line,no,broad,CC,adult,adult,fecundity 6-10 days (number of egg laid),fecundity 1-10 days (number of eggs laid),fertility,fertility,include_2,cor,0.95,NA,NA,NA,NA,NA,NA,NA,NA,"above-equator (pop EF, ED, CO, EA, NG)",table s6,fertility,fertility,genotype,1.831780823,39,1,1.831780823,female,adult,Insecta,within
1017,Drosophila melanogaster,153,rayyan-697472360,Age-specific patterns of genetic variance in Drosophila melanogaster .2. Fecundity and its genetic covariance with age-specific mortality,1996,1981,NA,lab,male,male,50,50,10,10,50,50,50,50,NA,NA,animal_model,genetic_line,no,narrow,authors,both,both,mortality in week 6,mortality in week 7,reverse_survival,reverse_survival,include,cor,NA,NA,NA,NA,NA,NA,NA,NA,NA,male,table 1,survival,survival,genotype,NA,10,1,NA,male,both,Insecta,within
1018,Drosophila melanogaster,243,rayyan-197247408,The genetic structure of female life history in D. melanogaster: Comparisons among populations,2000,NA,"Ohio, USA",lab,female,female,NA,NA,NA,NA,844,844,145,145,NA,NA,animal_model,full/half_sib,no,narrow,authors,adult,both,late fecundity,female survivorship,fertility,survival,include,cor,0.875,NA,NA,NA,NA,NA,NA,NA,NA,Bowling_Green_sib2,table 5,fertility,survival,family,1.354025101,844,1,1.354025101,female,cross,Insecta,between
1019,Drosophila melanogaster,243,rayyan-197247408,The genetic structure of female life history in D. melanogaster: Comparisons among populations,2000,NA,"Arizona, USA",lab,female,female,NA,NA,NA,NA,680,680,111,111,NA,NA,animal_model,full/half_sib,no,narrow,authors,non_adult,both,development rate (reciprocal of the develoment time of the first female to eclose),female survivorship,maturation,survival,include,cor,0.124,NA,NA,NA,NA,NA,NA,NA,NA,Flgstaff_sib1,table 5,maturation,survival,family,0.12464147,680,1,0.12464147,female,cross,Insecta,between
1020,Drosophila melanogaster,243,rayyan-197247408,The genetic structure of female life history in D. melanogaster: Comparisons among populations,2000,NA,"Arizona, California, Ohio, USA",lab,female,female,NA,NA,NA,NA,2372,2372,345,345,NA,NA,animal_model,full/half_sib,no,narrow,authors,adult,non_adult,early fecundity,development rate (reciprocal of the develoment time of the first female to eclose),fertility,maturation,include,cor,0.06,NA,NA,NA,NA,NA,NA,NA,NA,Flagstaff_Davis_Bowling_Green_combined_sib3,table 9,fertility,maturation,family,0.060072156,2372,1,0.060072156,female,cross,Insecta,between
1022,Drosophila melanogaster,243,rayyan-197247408,The genetic structure of female life history in D. melanogaster: Comparisons among populations,2000,NA,"Arizona, USA",lab,female,female,NA,NA,NA,NA,680,680,111,111,NA,NA,animal_model,full/half_sib,no,narrow,authors,adult,both,late fecundity,female survivorship,fertility,survival,include,cor,0.751,NA,NA,NA,NA,NA,NA,NA,NA,Flgstaff_sib1,table 5,fertility,survival,family,0.975244718,680,1,0.975244718,female,cross,Insecta,between
1023,Drosophila melanogaster,243,rayyan-197247408,The genetic structure of female life history in D. melanogaster: Comparisons among populations,2000,NA,"Arizona, California, Ohio, USA",lab,female,female,NA,NA,NA,NA,2372,2372,345,345,NA,NA,animal_model,full/half_sib,no,narrow,authors,non_adult,adult,development rate (reciprocal of the develoment time of the first female to eclose),late fecundity,maturation,fertility,include,cor,-0.31,NA,NA,NA,NA,NA,NA,NA,NA,Flagstaff_Davis_Bowling_Green_combined_sib3,table 9,maturation,fertility,family,-0.320545409,2372,1,-0.320545409,female,cross,Insecta,between
1024,Drosophila melanogaster,153,rayyan-697472360,Age-specific patterns of genetic variance in Drosophila melanogaster .2. Fecundity and its genetic covariance with age-specific mortality,1996,1981,NA,lab,female,female,50,50,10,10,50,50,50,50,NA,NA,animal_model,genetic_line,no,narrow,authors,both,both,mortality in week 5,mortality in week 6,reverse_survival,reverse_survival,include,cor,NA,NA,NA,NA,NA,NA,NA,NA,NA,female,table 1,survival,survival,genotype,NA,10,1,NA,female,both,Insecta,within
1025,Drosophila melanogaster,422,rayyan-697473383,The evolutionary costs of immunological maintenance and deployment,2008,2004,"Newfield, NY, USA",lab,female,female,NA,NA,40,40,NA,NA,NA,NA,NA,NA,line_mean_correlation,genetic_line,no,broad,CC,adult,adult,day 9 weight,weight gain (day 9 weight minus emergence weight),size,growth,include,cor,0.67,NA,NA,NA,NA,NA,NA,NA,NA,limited,table 3,size,growth,genotype,0.810743125,40,1,0.810743125,female,adult,Insecta,between
1026,Drosophila melanogaster,10,rayyan-178530589,Effects of temperature extremes on genetic variances for life history traits in Drosophila melanogaster as determined from parent-offspring comparisons,1998,1993,"Hstings, Australis",lab,both,female,94,94,NA,NA,94,94,94,94,376,188,family_mean_correlation,full_sib,no,broad,CC,non_adult,adult,egg-to-adult development time (days),eggs produced in the first 10 days,reverse_maturation,fertility,include,cor,0.168,NA,NA,NA,NA,NA,NA,NA,NA,28_progeny_28_parent,table 8,maturation,fertility,family,0.169607861,94,-1,-0.169607861,female,cross,Insecta,between
1028,Drosophila melanogaster,243,rayyan-197247408,The genetic structure of female life history in D. melanogaster: Comparisons among populations,2000,NA,"Ohio, USA",lab,female,female,NA,NA,NA,NA,810,810,129,129,NA,NA,animal_model,full/half_sib,no,narrow,authors,adult,non_adult,early fecundity,development rate (reciprocal of the develoment time of the first female to eclose),fertility,maturation,include,cor,-0.064,NA,NA,NA,NA,NA,NA,NA,NA,Bowling_Green_sib1,table 5,fertility,maturation,family,-0.064087597,810,1,-0.064087597,female,cross,Insecta,between
1029,Drosophila melanogaster,243,rayyan-197247408,The genetic structure of female life history in D. melanogaster: Comparisons among populations,2000,NA,"California, USA",lab,female,female,NA,NA,NA,NA,786,786,154,154,NA,NA,animal_model,full/half_sib,no,narrow,authors,adult,adult,early fecundity,late fecundity,fertility,fertility,include,cor,0.078,NA,NA,NA,NA,NA,NA,NA,NA,Davis_sib2,table 5,fertility,fertility,family,0.078158764,786,1,0.078158764,female,adult,Insecta,within
1031,Drosophila melanogaster,243,rayyan-197247408,The genetic structure of female life history in D. melanogaster: Comparisons among populations,2000,NA,"California, USA",lab,female,female,NA,NA,NA,NA,663,663,126,126,NA,NA,animal_model,full/half_sib,no,narrow,authors,adult,both,early fecundity,female survivorship,fertility,survival,include,cor,-0.342,NA,NA,NA,NA,NA,NA,NA,NA,Davis_sib1,table 5,fertility,survival,family,-0.356355693,663,1,-0.356355693,female,cross,Insecta,between
1032,Drosophila melanogaster,243,rayyan-197247408,The genetic structure of female life history in D. melanogaster: Comparisons among populations,2000,NA,"California, USA",lab,female,female,NA,NA,NA,NA,786,786,154,154,NA,NA,animal_model,full/half_sib,no,narrow,authors,adult,both,early fecundity,female survivorship,fertility,survival,include,cor,-0.281,NA,NA,NA,NA,NA,NA,NA,NA,Davis_sib2,table 5,fertility,survival,family,-0.288767472,786,1,-0.288767472,female,cross,Insecta,between
1034,Drosophila melanogaster,243,rayyan-197247408,The genetic structure of female life history in D. melanogaster: Comparisons among populations,2000,NA,"California, USA",lab,female,female,NA,NA,NA,NA,663,663,126,126,NA,NA,animal_model,full/half_sib,no,narrow,authors,non_adult,adult,development rate (reciprocal of the develoment time of the first female to eclose),late fecundity,maturation,fertility,include,cor,-0.543,NA,NA,NA,NA,NA,NA,NA,NA,Davis_sib1,table 5,maturation,fertility,family,-0.608400231,663,1,-0.608400231,female,cross,Insecta,between
1035,Drosophila melanogaster,153,rayyan-697472360,Age-specific patterns of genetic variance in Drosophila melanogaster .2. Fecundity and its genetic covariance with age-specific mortality,1996,1981,NA,lab,female,female,50,50,10,10,50,50,50,50,NA,NA,animal_model,genetic_line,no,narrow,authors,both,both,mortality in week 4,mortality in week 6,reverse_survival,reverse_survival,include,cor,0.749,NA,NA,NA,NA,NA,NA,NA,NA,female,table 1,survival,survival,genotype,0.970673268,10,1,0.970673268,female,both,Insecta,within
1036,Drosophila melanogaster,153,rayyan-697472360,Age-specific patterns of genetic variance in Drosophila melanogaster .2. Fecundity and its genetic covariance with age-specific mortality,1996,1981,NA,lab,female,female,50,50,10,10,50,50,50,50,NA,NA,animal_model,genetic_line,no,narrow,authors,both,both,mortality in week 4,mortality in week 7,reverse_survival,reverse_survival,include,cor,0.4008,NA,NA,NA,NA,NA,NA,NA,NA,female,table 1,survival,survival,genotype,0.424601674,10,1,0.424601674,female,both,Insecta,within
1037,Drosophila melanogaster,392,rayyan-697472974,Genetic variance for diapause expression and associated life histories in Drosophila melanogaster,2005,2001,"Walpole, Maine, USA",lab,female,female,NA,NA,30,30,NA,NA,NA,NA,600,600,line_mean_correlation,genetic_line,no,broad,CC,adult,adult,eggs/female days 1-7,eggs/female days 8-15,fertility,fertility,include,cor,0.2828,NA,NA,NA,NA,NA,NA,NA,NA,nondiapause,table 4,fertility,fertility,genotype,0.290722863,30,1,0.290722863,female,adult,Insecta,within
1038,Drosophila melanogaster,392,rayyan-697472974,Genetic variance for diapause expression and associated life histories in Drosophila melanogaster,2005,2001,"Walpole, Maine, USA",lab,female,female,NA,NA,30,30,NA,NA,NA,NA,600,600,line_mean_correlation,genetic_line,no,broad,CC,both,adult,lifespan,eggs/female days 1-7,survival,fertility,include,cor,0.1324,NA,NA,NA,NA,NA,NA,NA,NA,diapause,table 4,survival,fertility,genotype,0.133181887,30,1,0.133181887,female,cross,Insecta,between
1039,Drosophila melanogaster,392,rayyan-697472974,Genetic variance for diapause expression and associated life histories in Drosophila melanogaster,2005,2001,"Walpole, Maine, USA",lab,female,female,NA,NA,30,30,NA,NA,NA,NA,600,600,line_mean_correlation,genetic_line,no,broad,CC,both,adult,lifespan,eggs/female days 8-15,survival,fertility,include,cor,0.1957,NA,NA,NA,NA,NA,NA,NA,NA,diapause,table 4,survival,fertility,genotype,0.198257367,30,1,0.198257367,female,cross,Insecta,between
1041,Drosophila melanogaster,243,rayyan-197247408,The genetic structure of female life history in D. melanogaster: Comparisons among populations,2000,NA,"Ohio, USA",lab,female,female,NA,NA,NA,NA,844,844,145,145,NA,NA,animal_model,full/half_sib,no,narrow,authors,non_adult,both,development rate (reciprocal of the develoment time of the first female to eclose),female survivorship,maturation,survival,include,cor,0.303,NA,NA,NA,NA,NA,NA,NA,NA,Bowling_Green_sib2,table 5,maturation,survival,family,0.312819583,844,1,0.312819583,female,cross,Insecta,between
1042,Drosophila melanogaster,243,rayyan-197247408,The genetic structure of female life history in D. melanogaster: Comparisons among populations,2000,NA,"Ohio, USA",lab,female,female,NA,NA,NA,NA,844,844,145,145,NA,NA,animal_model,full/half_sib,no,narrow,authors,adult,non_adult,early fecundity,development rate (reciprocal of the develoment time of the first female to eclose),fertility,maturation,include,cor,-0.145,NA,NA,NA,NA,NA,NA,NA,NA,Bowling_Green_sib2,table 5,fertility,maturation,family,-0.146029224,844,1,-0.146029224,female,cross,Insecta,between
1043,Drosophila melanogaster,243,rayyan-197247408,The genetic structure of female life history in D. melanogaster: Comparisons among populations,2000,NA,"Ohio, USA",lab,female,female,NA,NA,NA,NA,810,810,129,129,NA,NA,animal_model,full/half_sib,no,narrow,authors,adult,both,late fecundity,female survivorship,fertility,survival,include,cor,0.85,NA,NA,NA,NA,NA,NA,NA,NA,Bowling_Green_sib1,table 5,fertility,survival,family,1.256152812,810,1,1.256152812,female,cross,Insecta,between
1044,Drosophila melanogaster,243,rayyan-197247408,The genetic structure of female life history in D. melanogaster: Comparisons among populations,2000,NA,"Ohio, USA",lab,female,female,NA,NA,NA,NA,810,810,129,129,NA,NA,animal_model,full/half_sib,no,narrow,authors,adult,adult,early fecundity,late fecundity,fertility,fertility,include,cor,0.136,NA,NA,NA,NA,NA,NA,NA,NA,Bowling_Green_sib1,table 5,fertility,fertility,family,0.136847915,810,1,0.136847915,female,adult,Insecta,within
1045,Drosophila melanogaster,243,rayyan-197247408,The genetic structure of female life history in D. melanogaster: Comparisons among populations,2000,NA,"Ohio, USA",lab,female,female,NA,NA,NA,NA,844,844,145,145,NA,NA,animal_model,full/half_sib,no,narrow,authors,adult,adult,early fecundity,late fecundity,fertility,fertility,include,cor,-0.12,NA,NA,NA,NA,NA,NA,NA,NA,Bowling_Green_sib2,table 5,fertility,fertility,family,-0.120581028,844,1,-0.120581028,female,adult,Insecta,within
1047,Drosophila melanogaster,243,rayyan-197247408,The genetic structure of female life history in D. melanogaster: Comparisons among populations,2000,NA,"Ohio, USA",lab,female,female,NA,NA,NA,NA,810,810,129,129,NA,NA,animal_model,full/half_sib,no,narrow,authors,adult,both,early fecundity,female survivorship,fertility,survival,include,cor,-0.289,NA,NA,NA,NA,NA,NA,NA,NA,Bowling_Green_sib1,table 5,fertility,survival,family,-0.297474787,810,1,-0.297474787,female,cross,Insecta,between
1048,Drosophila melanogaster,392,rayyan-697472974,Genetic variance for diapause expression and associated life histories in Drosophila melanogaster,2005,2001,"Walpole, Maine, USA",lab,female,female,NA,NA,30,30,NA,NA,NA,NA,600,600,line_mean_correlation,genetic_line,no,broad,CC,both,adult,lifespan,eggs/female days 1-7,survival,fertility,include,cor,-0.2231,NA,NA,NA,NA,NA,NA,NA,NA,nondiapause,table 4,survival,fertility,genotype,-0.226916128,30,1,-0.226916128,female,cross,Insecta,between
1049,Drosophila melanogaster,392,rayyan-697472974,Genetic variance for diapause expression and associated life histories in Drosophila melanogaster,2005,2001,"Walpole, Maine, USA",lab,female,female,NA,NA,30,30,NA,NA,NA,NA,600,600,line_mean_correlation,genetic_line,no,broad,CC,both,adult,lifespan,eggs/female days 8-15,survival,fertility,include,cor,-0.0035,NA,NA,NA,NA,NA,NA,NA,NA,nondiapause,table 4,survival,fertility,genotype,-0.003500014,30,1,-0.003500014,female,cross,Insecta,between
1050,Drosophila melanogaster,243,rayyan-197247408,The genetic structure of female life history in D. melanogaster: Comparisons among populations,2000,NA,"Arizona, USA",lab,female,female,NA,NA,NA,NA,644,644,97,97,NA,NA,animal_model,full/half_sib,no,narrow,authors,adult,both,late fecundity,female survivorship,fertility,survival,include,cor,0.952,NA,NA,NA,NA,NA,NA,NA,NA,Flgstaff_sib2,table 5,fertility,survival,family,1.852704378,644,1,1.852704378,female,cross,Insecta,between
1051,Drosophila melanogaster,10,rayyan-178530589,Effects of temperature extremes on genetic variances for life history traits in Drosophila melanogaster as determined from parent-offspring comparisons,1998,1993,"Hstings, Australis",lab,both,female,116,116,NA,NA,116,116,116,116,376,232,family_mean_correlation,full_sib,no,broad,CC,non_adult,adult,egg-to-adult development time (days),eggs produced in the first 10 days,reverse_maturation,fertility,include,cor,-0.562,NA,NA,NA,NA,NA,NA,NA,NA,25_progeny_14_parent,table 8,maturation,fertility,family,-0.63575171,116,-1,0.63575171,female,cross,Insecta,between
1052,Drosophila melanogaster,10,rayyan-178530589,Effects of temperature extremes on genetic variances for life history traits in Drosophila melanogaster as determined from parent-offspring comparisons,1998,1993,"Hstings, Australis",lab,both,female,96,96,NA,NA,96,96,96,96,376,192,family_mean_correlation,full_sib,no,broad,CC,non_adult,adult,egg-to-adult development time (days),eggs produced in the first 10 days,reverse_maturation,fertility,include,cor,-0.107,NA,NA,NA,NA,NA,NA,NA,NA,25_progeny_28_parent,table 8,maturation,fertility,family,-0.107411176,96,-1,0.107411176,female,cross,Insecta,between
1053,Drosophila melanogaster,243,rayyan-197247408,The genetic structure of female life history in D. melanogaster: Comparisons among populations,2000,NA,"Arizona, USA",lab,female,female,NA,NA,NA,NA,644,644,97,97,NA,NA,animal_model,full/half_sib,no,narrow,authors,adult,both,early fecundity,female survivorship,fertility,survival,include,cor,0.048,NA,NA,NA,NA,NA,NA,NA,NA,Flgstaff_sib2,table 5,fertility,survival,family,0.048036915,644,1,0.048036915,female,cross,Insecta,between
1054,Drosophila melanogaster,422,rayyan-697473383,The evolutionary costs of immunological maintenance and deployment,2008,2004,"Newfield, NY, USA",lab,female,female,NA,NA,40,40,NA,NA,NA,NA,NA,NA,line_mean_correlation,genetic_line,no,broad,CC,adult,adult,weight gain (day 9 weight minus emergence weight),emergence weight,growth,size,include,cor,-0.424,NA,NA,NA,NA,NA,NA,NA,NA,unlimited,table 3,growth,size,genotype,-0.452558716,40,1,-0.452558716,female,adult,Insecta,between
1056,Drosophila melanogaster,149,rayyan-697472291,"Evolutionary responses of Drosophila melanogaster to selection at different larval densities: changes in genetic variation, specialization and phenotypic plasticity",2002,1991,"Galicia, Spain",lab,both,both,60,60,6,6,60,60,60,60,600,600,animal_model,pedigree,yes,narrow,authors,non_adult,non_adult,biomass (total pupal weight),average pupa weight ,size,size,include,cor,0.082,NA,NA,NA,NA,NA,NA,NA,NA,high,table 2,size,size,pedigree,0.082184534,600,1,0.082184534,both,non_adult,Insecta,within
1057,Drosophila melanogaster,153,rayyan-697472360,Age-specific patterns of genetic variance in Drosophila melanogaster .2. Fecundity and its genetic covariance with age-specific mortality,1996,1981,NA,lab,male,male,50,50,10,10,50,50,50,50,NA,NA,animal_model,genetic_line,no,narrow,authors,both,both,mortality in week 5,mortality in week 8,reverse_survival,reverse_survival,include,cor,0.0485,NA,NA,NA,NA,NA,NA,NA,NA,male,table 1,survival,survival,genotype,0.048538082,10,1,0.048538082,male,both,Insecta,within
1059,Drosophila melanogaster,149,rayyan-697472291,"Evolutionary responses of Drosophila melanogaster to selection at different larval densities: changes in genetic variation, specialization and phenotypic plasticity",2002,1991,"Galicia, Spain",lab,both,both,60,60,6,6,60,60,60,60,600,600,animal_model,pedigree,yes,narrow,authors,non_adult,non_adult,larva-to-pupa viability,average pupation day (developmental time),survival,reverse_maturation,include,cor,0.033,NA,NA,NA,NA,NA,NA,NA,NA,high,table 2,survival,maturation,pedigree,0.033011987,600,-1,-0.033011987,both,non_adult,Insecta,between
1060,Drosophila melanogaster,243,rayyan-197247408,The genetic structure of female life history in D. melanogaster: Comparisons among populations,2000,NA,"Arizona, USA",lab,female,female,NA,NA,NA,NA,644,644,97,97,NA,NA,animal_model,full/half_sib,no,narrow,authors,non_adult,both,development rate (reciprocal of the develoment time of the first female to eclose),female survivorship,maturation,survival,include,cor,0.373,NA,NA,NA,NA,NA,NA,NA,NA,Flgstaff_sib2,table 5,maturation,survival,family,0.391903433,644,1,0.391903433,female,cross,Insecta,between
1061,Drosophila melanogaster,390,rayyan-697472972,Quantitative trait loci with age-specific effects on fecundity in Drosophila melanogaster,2006,NA,NA,lab,female,female,NA,NA,92,92,NA,NA,NA,NA,1380,1380,animal_model,genetic_line,no,broad,CC,adult,adult,fecundity at week 1,fecundity at week 4,fertility,fertility,include,cor,0.05,"[-0.11, 0.30]",95CI,NA,NA,NA,NA,NA,NA,rayyan-697472972,table 1,fertility,fertility,genotype,0.050041729,92,1,0.050041729,female,adult,Insecta,within
1062,Drosophila melanogaster,243,rayyan-197247408,The genetic structure of female life history in D. melanogaster: Comparisons among populations,2000,NA,"California, USA",lab,female,female,NA,NA,NA,NA,786,786,154,154,NA,NA,animal_model,full/half_sib,no,narrow,authors,non_adult,adult,development rate (reciprocal of the develoment time of the first female to eclose),late fecundity,maturation,fertility,include,cor,-0.5,NA,NA,NA,NA,NA,NA,NA,NA,Davis_sib2,table 5,maturation,fertility,family,-0.549306144,786,1,-0.549306144,female,cross,Insecta,between
1063,Drosophila melanogaster,10,rayyan-178530589,Effects of temperature extremes on genetic variances for life history traits in Drosophila melanogaster as determined from parent-offspring comparisons,1998,1993,"Hstings, Australis",lab,both,female,98,98,NA,NA,98,98,98,98,376,196,family_mean_correlation,full_sib,no,broad,CC,non_adult,adult,egg-to-adult development time (days),eggs produced in the first 10 days,reverse_maturation,fertility,include,cor,-0.32,NA,NA,NA,NA,NA,NA,NA,NA,14_progeny_28_parent,table 8,maturation,fertility,family,-0.331647109,98,-1,0.331647109,female,cross,Insecta,between
1064,Drosophila melanogaster,149,rayyan-697472291,"Evolutionary responses of Drosophila melanogaster to selection at different larval densities: changes in genetic variation, specialization and phenotypic plasticity",2002,1991,"Galicia, Spain",lab,both,both,60,60,6,6,60,60,60,60,600,600,animal_model,pedigree,yes,narrow,authors,non_adult,non_adult,larva-to-pupa viability,average pupa weight ,survival,size,include,cor,-0.352,NA,NA,NA,NA,NA,NA,NA,NA,intermediate,table 2,survival,size,pedigree,-0.36772478,600,1,-0.36772478,both,non_adult,Insecta,between
1065,Drosophila melanogaster,149,rayyan-697472291,"Evolutionary responses of Drosophila melanogaster to selection at different larval densities: changes in genetic variation, specialization and phenotypic plasticity",2002,1991,"Galicia, Spain",lab,both,both,60,60,6,6,60,60,60,60,600,600,animal_model,pedigree,yes,narrow,authors,non_adult,non_adult,larva-to-pupa viability,average pupation day (developmental time),survival,reverse_maturation,include,cor,0.032,NA,NA,NA,NA,NA,NA,NA,NA,intermediate,table 2,survival,maturation,pedigree,0.032010929,600,-1,-0.032010929,both,non_adult,Insecta,between
1066,Drosophila melanogaster,422,rayyan-697473383,The evolutionary costs of immunological maintenance and deployment,2008,2004,"Newfield, NY, USA",lab,female,female,NA,NA,40,40,NA,NA,NA,NA,NA,NA,line_mean_correlation,genetic_line,no,broad,CC,adult,adult,day 9 weight,emergence weight,size,size,include,cor,0.324,NA,NA,NA,NA,NA,NA,NA,NA,limited,table 3,size,size,genotype,0.33610983,40,1,0.33610983,female,adult,Insecta,within
1067,Drosophila melanogaster,243,rayyan-197247408,The genetic structure of female life history in D. melanogaster: Comparisons among populations,2000,NA,"Arizona, USA",lab,female,female,NA,NA,NA,NA,680,680,111,111,NA,NA,animal_model,full/half_sib,no,narrow,authors,adult,both,early fecundity,female survivorship,fertility,survival,include,cor,0.281,NA,NA,NA,NA,NA,NA,NA,NA,Flgstaff_sib1,table 5,fertility,survival,family,0.288767472,680,1,0.288767472,female,cross,Insecta,between
1068,Drosophila melanogaster,422,rayyan-697473383,The evolutionary costs of immunological maintenance and deployment,2008,2004,"Newfield, NY, USA",lab,female,female,NA,NA,40,40,NA,NA,NA,NA,NA,NA,line_mean_correlation,genetic_line,no,broad,CC,adult,adult,weight gain (day 9 weight minus emergence weight),emergence weight,growth,size,include,cor,-0.482,NA,NA,NA,NA,NA,NA,NA,NA,limited,table 3,growth,size,genotype,-0.525586282,40,1,-0.525586282,female,adult,Insecta,between
1069,Drosophila melanogaster,243,rayyan-197247408,The genetic structure of female life history in D. melanogaster: Comparisons among populations,2000,NA,"Arizona, USA",lab,female,female,NA,NA,NA,NA,680,680,111,111,NA,NA,animal_model,full/half_sib,no,narrow,authors,non_adult,adult,development rate (reciprocal of the develoment time of the first female to eclose),late fecundity,maturation,fertility,include,cor,-0.057,NA,NA,NA,NA,NA,NA,NA,NA,Flgstaff_sib1,table 5,maturation,fertility,family,-0.057061852,680,1,-0.057061852,female,cross,Insecta,between
1070,Drosophila melanogaster,149,rayyan-697472291,"Evolutionary responses of Drosophila melanogaster to selection at different larval densities: changes in genetic variation, specialization and phenotypic plasticity",2002,1991,"Galicia, Spain",lab,both,both,60,60,6,6,60,60,60,60,600,600,animal_model,pedigree,yes,narrow,authors,non_adult,non_adult,biomass (total pupal weight),average pupation day (developmental time),size,reverse_maturation,include,cor,-0.043,NA,NA,NA,NA,NA,NA,NA,NA,high,table 2,size,maturation,pedigree,-0.043026532,600,-1,0.043026532,both,non_adult,Insecta,between
1071,Drosophila melanogaster,133,rayyan-697472023,Quantitative genetics of learning ability and resistance to stress in Drosophila melanogaster,2015,2007,"Valais, Switzerland",lab,both,both,288,288,12,12,4320,4320,2880,2880,NA,NA,animal_model,full_sib,no,narrow,authors,non_adult,non_adult,egg-to-adult viability,developmental rate,survival,maturation,include,cor,-0.296,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-697472023,fig 3,survival,maturation,family,-0.30512976,288,1,-0.30512976,both,non_adult,Insecta,between
1072,Drosophila melanogaster,149,rayyan-697472291,"Evolutionary responses of Drosophila melanogaster to selection at different larval densities: changes in genetic variation, specialization and phenotypic plasticity",2002,1991,"Galicia, Spain",lab,both,both,60,60,6,6,60,60,60,60,600,600,animal_model,pedigree,yes,narrow,authors,non_adult,non_adult,biomass (total pupal weight),average pupation day (developmental time),size,reverse_maturation,include,cor,0.02,NA,NA,NA,NA,NA,NA,NA,NA,intermediate,table 2,size,maturation,pedigree,0.020002667,600,-1,-0.020002667,both,non_adult,Insecta,between
1073,Drosophila melanogaster,149,rayyan-697472291,"Evolutionary responses of Drosophila melanogaster to selection at different larval densities: changes in genetic variation, specialization and phenotypic plasticity",2002,1991,"Galicia, Spain",lab,both,both,60,60,6,6,60,60,60,60,600,600,animal_model,pedigree,yes,narrow,authors,non_adult,non_adult,average pupa weight ,average pupation day (developmental time),size,reverse_maturation,include,cor,0,NA,NA,NA,NA,NA,NA,NA,NA,high,table 2,size,maturation,pedigree,0,600,-1,0,both,non_adult,Insecta,between
1075,Drosophila melanogaster,149,rayyan-697472291,"Evolutionary responses of Drosophila melanogaster to selection at different larval densities: changes in genetic variation, specialization and phenotypic plasticity",2002,1991,"Galicia, Spain",lab,both,both,60,60,6,6,60,60,60,60,600,600,animal_model,pedigree,yes,narrow,authors,non_adult,non_adult,biomass (total pupal weight),average pupa weight ,size,size,include,cor,-0.059,NA,NA,NA,NA,NA,NA,NA,NA,intermediate,table 2,size,size,pedigree,-0.059068603,600,1,-0.059068603,both,non_adult,Insecta,within
1076,Drosophila melanogaster,10,rayyan-178530589,Effects of temperature extremes on genetic variances for life history traits in Drosophila melanogaster as determined from parent-offspring comparisons,1998,1993,"Hstings, Australis",lab,both,female,106,106,NA,NA,106,106,106,106,376,212,family_mean_correlation,full_sib,no,broad,CC,non_adult,adult,egg-to-adult development time (days),eggs produced in the first 10 days,reverse_maturation,fertility,include,cor,-0.536,NA,NA,NA,NA,NA,NA,NA,NA,28_progeny_14_parent,table 8,maturation,fertility,family,-0.598526181,106,-1,0.598526181,female,cross,Insecta,between
1078,Drosophila melanogaster,243,rayyan-197247408,The genetic structure of female life history in D. melanogaster: Comparisons among populations,2000,NA,"California, USA",lab,female,female,NA,NA,NA,NA,786,786,154,154,NA,NA,animal_model,full/half_sib,no,narrow,authors,adult,both,late fecundity,female survivorship,fertility,survival,include,cor,-0.024,NA,NA,NA,NA,NA,NA,NA,NA,Davis_sib2,table 5,fertility,survival,family,-0.02400461,786,1,-0.02400461,female,cross,Insecta,between
1079,Drosophila melanogaster,149,rayyan-697472291,"Evolutionary responses of Drosophila melanogaster to selection at different larval densities: changes in genetic variation, specialization and phenotypic plasticity",2002,1991,"Galicia, Spain",lab,both,both,60,60,6,6,60,60,60,60,600,600,animal_model,pedigree,yes,narrow,authors,non_adult,non_adult,average pupa weight ,average pupation day (developmental time),size,reverse_maturation,include,cor,-0.108,NA,NA,NA,NA,NA,NA,NA,NA,intermediate,table 2,size,maturation,pedigree,-0.108422867,600,-1,0.108422867,both,non_adult,Insecta,between
1080,Drosophila melanogaster,149,rayyan-697472291,"Evolutionary responses of Drosophila melanogaster to selection at different larval densities: changes in genetic variation, specialization and phenotypic plasticity",2002,1991,"Galicia, Spain",lab,both,both,60,60,6,6,60,60,60,60,600,600,animal_model,pedigree,yes,narrow,authors,non_adult,non_adult,biomass (total pupal weight),larva-to-pupa viability,size,survival,include,cor,0.25,NA,NA,NA,NA,NA,NA,NA,NA,high,table 2,size,survival,pedigree,0.255412812,600,1,0.255412812,both,non_adult,Insecta,between
1082,Drosophila melanogaster,149,rayyan-697472291,"Evolutionary responses of Drosophila melanogaster to selection at different larval densities: changes in genetic variation, specialization and phenotypic plasticity",2002,1991,"Galicia, Spain",lab,both,both,60,60,6,6,60,60,60,60,600,600,animal_model,pedigree,yes,narrow,authors,non_adult,non_adult,larva-to-pupa viability,average pupa weight ,survival,size,include,cor,-0.226,NA,NA,NA,NA,NA,NA,NA,NA,high,table 2,survival,size,pedigree,-0.229970121,600,1,-0.229970121,both,non_adult,Insecta,between
1083,Drosophila melanogaster,243,rayyan-197247408,The genetic structure of female life history in D. melanogaster: Comparisons among populations,2000,NA,"Arizona, USA",lab,female,female,NA,NA,NA,NA,644,644,97,97,NA,NA,animal_model,full/half_sib,no,narrow,authors,non_adult,adult,development rate (reciprocal of the develoment time of the first female to eclose),late fecundity,maturation,fertility,include,cor,0.301,NA,NA,NA,NA,NA,NA,NA,NA,Flgstaff_sib2,table 5,maturation,fertility,family,0.310618868,644,1,0.310618868,female,cross,Insecta,between
1084,Drosophila melanogaster,149,rayyan-697472291,"Evolutionary responses of Drosophila melanogaster to selection at different larval densities: changes in genetic variation, specialization and phenotypic plasticity",2002,1991,"Galicia, Spain",lab,both,both,60,60,6,6,60,60,60,60,600,600,animal_model,pedigree,yes,narrow,authors,non_adult,non_adult,biomass (total pupal weight),larva-to-pupa viability,size,survival,include,cor,0.313,NA,NA,NA,NA,NA,NA,NA,NA,intermediate,table 2,size,survival,pedigree,0.323867791,600,1,0.323867791,both,non_adult,Insecta,between
1085,Drosophila melanogaster,243,rayyan-197247408,The genetic structure of female life history in D. melanogaster: Comparisons among populations,2000,NA,"Arizona, USA",lab,female,female,NA,NA,NA,NA,644,644,97,97,NA,NA,animal_model,full/half_sib,no,narrow,authors,adult,non_adult,early fecundity,development rate (reciprocal of the develoment time of the first female to eclose),fertility,maturation,include,cor,-0.554,NA,NA,NA,NA,NA,NA,NA,NA,Flgstaff_sib2,table 5,fertility,maturation,family,-0.624134289,644,1,-0.624134289,female,cross,Insecta,between
1086,Drosophila melanogaster,243,rayyan-197247408,The genetic structure of female life history in D. melanogaster: Comparisons among populations,2000,NA,"California, USA",lab,female,female,NA,NA,NA,NA,663,663,126,126,NA,NA,animal_model,full/half_sib,no,narrow,authors,adult,both,late fecundity,female survivorship,fertility,survival,include,cor,0.354,NA,NA,NA,NA,NA,NA,NA,NA,Davis_sib1,table 5,fertility,survival,family,0.370009475,663,1,0.370009475,female,cross,Insecta,between
1087,Drosophila melanogaster,243,rayyan-197247408,The genetic structure of female life history in D. melanogaster: Comparisons among populations,2000,NA,"Arizona, USA",lab,female,female,NA,NA,NA,NA,680,680,111,111,NA,NA,animal_model,full/half_sib,no,narrow,authors,adult,adult,early fecundity,late fecundity,fertility,fertility,include,cor,0.574,NA,NA,NA,NA,NA,NA,NA,NA,Flgstaff_sib1,table 5,fertility,fertility,family,0.653468041,680,1,0.653468041,female,adult,Insecta,within
1088,Drosophila melanogaster,243,rayyan-197247408,The genetic structure of female life history in D. melanogaster: Comparisons among populations,2000,NA,"California, USA",lab,female,female,NA,NA,NA,NA,663,663,126,126,NA,NA,animal_model,full/half_sib,no,narrow,authors,non_adult,both,development rate (reciprocal of the develoment time of the first female to eclose),female survivorship,maturation,survival,include,cor,0.502,NA,NA,NA,NA,NA,NA,NA,NA,Davis_sib1,table 5,maturation,survival,family,0.551976378,663,1,0.551976378,female,cross,Insecta,between
1090,Drosophila melanogaster,243,rayyan-197247408,The genetic structure of female life history in D. melanogaster: Comparisons among populations,2000,NA,"Arizona, USA",lab,female,female,NA,NA,NA,NA,680,680,111,111,NA,NA,animal_model,full/half_sib,no,narrow,authors,adult,non_adult,early fecundity,development rate (reciprocal of the develoment time of the first female to eclose),fertility,maturation,include,cor,0.215,NA,NA,NA,NA,NA,NA,NA,NA,Flgstaff_sib1,table 5,fertility,maturation,family,0.218407819,680,1,0.218407819,female,cross,Insecta,between
1092,Drosophila melanogaster,243,rayyan-197247408,The genetic structure of female life history in D. melanogaster: Comparisons among populations,2000,NA,"Arizona, USA",lab,female,female,NA,NA,NA,NA,644,644,97,97,NA,NA,animal_model,full/half_sib,no,narrow,authors,adult,adult,early fecundity,late fecundity,fertility,fertility,include,cor,-0.157,NA,NA,NA,NA,NA,NA,NA,NA,Flgstaff_sib2,table 5,fertility,fertility,family,-0.158309385,644,1,-0.158309385,female,adult,Insecta,within
1093,Drosophila melanogaster,243,rayyan-197247408,The genetic structure of female life history in D. melanogaster: Comparisons among populations,2000,NA,"California, USA",lab,female,female,NA,NA,NA,NA,786,786,154,154,NA,NA,animal_model,full/half_sib,no,narrow,authors,non_adult,both,development rate (reciprocal of the develoment time of the first female to eclose),female survivorship,maturation,survival,include,cor,-0.248,NA,NA,NA,NA,NA,NA,NA,NA,Davis_sib2,table 5,maturation,survival,family,-0.253280612,786,1,-0.253280612,female,cross,Insecta,between
1094,Drosophila serrata,275,rayyan-197247618,Dominance Genetic Variance for Traits Under Directional Selection in Drosophila serrata,2015,NA,NA,lab,male,male,666,685,NA,NA,666,685,666,685,2800,5000,animal_model,full/half_sib,no,narrow,authors,adult,adult,fitness (odds ratio of focal male to competitor-male offspring sired),wing trait alm2-8,fertility,size,include,cor,-0.369,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-197247618,table 2,fertility,size,family,-0.387264981,666,1,-0.387264981,male,adult,Insecta,between
1095,Drosophila serrata,275,rayyan-197247618,Dominance Genetic Variance for Traits Under Directional Selection in Drosophila serrata,2015,NA,NA,lab,male,male,666,685,NA,NA,666,685,666,685,2800,5000,animal_model,full/half_sib,no,dominance,authors,adult,adult,fitness (odds ratio of focal male to competitor-male offspring sired),wing trait alm2-4,fertility,size,include,cor,-0.17,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-197247618,table 3,fertility,size,family,-0.171666664,666,1,-0.171666664,male,adult,Insecta,between
1096,Drosophila serrata,275,rayyan-197247618,Dominance Genetic Variance for Traits Under Directional Selection in Drosophila serrata,2015,NA,NA,lab,male,male,666,685,NA,NA,666,685,666,685,2800,5000,animal_model,full/half_sib,no,dominance,authors,adult,adult,fitness (odds ratio of focal male to competitor-male offspring sired),wing trait alm2-8,fertility,size,include,cor,0.097,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-197247618,table 3,fertility,size,family,0.097305953,666,1,0.097305953,male,adult,Insecta,between
1097,Drosophila serrata,275,rayyan-197247618,Dominance Genetic Variance for Traits Under Directional Selection in Drosophila serrata,2015,NA,NA,lab,male,male,666,685,NA,NA,666,685,666,685,2800,5000,animal_model,full/half_sib,no,narrow,authors,adult,adult,fitness (odds ratio of focal male to competitor-male offspring sired),wing trait alm4-5,fertility,size,include,cor,0.473,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-197247618,table 2,fertility,size,family,0.513927934,666,1,0.513927934,male,adult,Insecta,between
1098,Drosophila serrata,275,rayyan-197247618,Dominance Genetic Variance for Traits Under Directional Selection in Drosophila serrata,2015,NA,NA,lab,male,male,666,685,NA,NA,666,685,666,685,2800,5000,animal_model,full/half_sib,no,dominance,authors,adult,adult,fitness (odds ratio of focal male to competitor-male offspring sired),wing trait alm2-5,fertility,size,include,cor,-0.114,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-197247618,table 3,fertility,size,family,-0.114497735,666,1,-0.114497735,male,adult,Insecta,between
1099,Drosophila serrata,275,rayyan-197247618,Dominance Genetic Variance for Traits Under Directional Selection in Drosophila serrata,2015,NA,NA,lab,male,male,666,685,NA,NA,666,685,666,685,2800,5000,animal_model,full/half_sib,no,narrow,authors,adult,adult,fitness (odds ratio of focal male to competitor-male offspring sired),wing trait alm2-5,fertility,size,include,cor,0.344,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-197247618,table 2,fertility,size,family,0.358622366,666,1,0.358622366,male,adult,Insecta,between
1100,Drosophila serrata,275,rayyan-197247618,Dominance Genetic Variance for Traits Under Directional Selection in Drosophila serrata,2015,NA,NA,lab,male,male,666,685,NA,NA,666,685,666,685,2800,5000,animal_model,full/half_sib,no,narrow,authors,adult,adult,fitness (odds ratio of focal male to competitor-male offspring sired),wing trait alm5-8,fertility,size,include,cor,-0.292,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-197247618,table 2,fertility,size,family,-0.300751295,666,1,-0.300751295,male,adult,Insecta,between
1101,Drosophila serrata,275,rayyan-197247618,Dominance Genetic Variance for Traits Under Directional Selection in Drosophila serrata,2015,NA,NA,lab,male,male,666,685,NA,NA,666,685,666,685,2800,5000,animal_model,full/half_sib,no,narrow,authors,adult,adult,fitness (odds ratio of focal male to competitor-male offspring sired),wing trait alm5-6,fertility,size,include,cor,-0.382,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-197247618,table 2,fertility,size,family,-0.402399273,666,1,-0.402399273,male,adult,Insecta,between
1102,Drosophila serrata,275,rayyan-197247618,Dominance Genetic Variance for Traits Under Directional Selection in Drosophila serrata,2015,NA,NA,lab,male,male,666,685,NA,NA,666,685,666,685,2800,5000,animal_model,full/half_sib,no,narrow,authors,adult,adult,fitness (odds ratio of focal male to competitor-male offspring sired),wing trait alm3-9,fertility,size,include,cor,0.593,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-197247618,table 2,fertility,size,family,0.682280562,666,1,0.682280562,male,adult,Insecta,between
1103,Drosophila serrata,275,rayyan-197247618,Dominance Genetic Variance for Traits Under Directional Selection in Drosophila serrata,2015,NA,NA,lab,male,male,666,685,NA,NA,666,685,666,685,2800,5000,animal_model,full/half_sib,no,dominance,authors,adult,adult,fitness (odds ratio of focal male to competitor-male offspring sired),wing trait alm3-9,fertility,size,include,cor,0.045,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-197247618,table 3,fertility,size,family,0.045030412,666,1,0.045030412,male,adult,Insecta,between
1104,Drosophila serrata,275,rayyan-197247618,Dominance Genetic Variance for Traits Under Directional Selection in Drosophila serrata,2015,NA,NA,lab,male,male,666,685,NA,NA,666,685,666,685,2800,5000,animal_model,full/half_sib,no,dominance,authors,adult,adult,fitness (odds ratio of focal male to competitor-male offspring sired),wing trait alm4-5,fertility,size,include,cor,-0.131,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-197247618,table 3,fertility,size,family,-0.131757175,666,1,-0.131757175,male,adult,Insecta,between
1105,Drosophila serrata,275,rayyan-197247618,Dominance Genetic Variance for Traits Under Directional Selection in Drosophila serrata,2015,NA,NA,lab,male,male,666,685,NA,NA,666,685,666,685,2800,5000,animal_model,full/half_sib,no,narrow,authors,adult,adult,fitness (odds ratio of focal male to competitor-male offspring sired),wing trait alm3-7,fertility,size,include,cor,0.012,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-197247618,table 2,fertility,size,family,0.012000576,666,1,0.012000576,male,adult,Insecta,between
1106,Drosophila serrata,275,rayyan-197247618,Dominance Genetic Variance for Traits Under Directional Selection in Drosophila serrata,2015,NA,NA,lab,male,male,666,685,NA,NA,666,685,666,685,2800,5000,animal_model,full/half_sib,no,dominance,authors,adult,adult,fitness (odds ratio of focal male to competitor-male offspring sired),wing trait alm5-8,fertility,size,include,cor,0.226,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-197247618,table 3,fertility,size,family,0.229970121,666,1,0.229970121,male,adult,Insecta,between
1107,Drosophila serrata,275,rayyan-197247618,Dominance Genetic Variance for Traits Under Directional Selection in Drosophila serrata,2015,NA,NA,lab,male,male,666,685,NA,NA,666,685,666,685,2800,5000,animal_model,full/half_sib,no,narrow,authors,adult,adult,fitness (odds ratio of focal male to competitor-male offspring sired),wing trait alm2-4,fertility,size,include,cor,0.599,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-197247618,table 2,fertility,size,family,0.691586143,666,1,0.691586143,male,adult,Insecta,between
1108,Drosophila serrata,275,rayyan-197247618,Dominance Genetic Variance for Traits Under Directional Selection in Drosophila serrata,2015,NA,NA,lab,male,male,666,685,NA,NA,666,685,666,685,2800,5000,animal_model,full/half_sib,no,dominance,authors,adult,adult,fitness (odds ratio of focal male to competitor-male offspring sired),wing trait alm5-6,fertility,size,include,cor,0.532,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-197247618,table 3,fertility,size,family,0.592930527,666,1,0.592930527,male,adult,Insecta,between
1109,Drosophila serrata,275,rayyan-197247618,Dominance Genetic Variance for Traits Under Directional Selection in Drosophila serrata,2015,NA,NA,lab,male,male,666,685,NA,NA,666,685,666,685,2800,5000,animal_model,full/half_sib,no,dominance,authors,adult,adult,fitness (odds ratio of focal male to competitor-male offspring sired),wing trait alm3-7,fertility,size,include,cor,0.044,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-197247618,table 3,fertility,size,family,0.044028428,666,1,0.044028428,male,adult,Insecta,between
1110,Drosophila simulans,167,rayyan-197247019,Few genetic and environmental correlations between life history and stress resistance traits affect adaptation to fluctuating thermal regimes,2016,2012,"Bologna, Italy",lab,female,both,NA,NA,21,21,NA,NA,NA,NA,210,840,line_mean_correlation,genetic_line,yes,broad,authors,adult,non_adult,body size (female right wing),developmental time ,size,reverse_maturation,include,cor,-0.21,NA,NA,NA,NA,NA,NA,NA,NA,constant_selection_test_on_predictable_fluctuating,table 2,size,maturation,genotype,-0.213171347,21,-1,0.213171347,female,cross,Insecta,between
1111,Drosophila simulans,167,rayyan-197247019,Few genetic and environmental correlations between life history and stress resistance traits affect adaptation to fluctuating thermal regimes,2016,2012,"Bologna, Italy",lab,female,female,NA,NA,21,21,NA,NA,NA,NA,210,210,line_mean_correlation,genetic_line,yes,broad,authors,adult,adult,productivity,body size (female right wing),fertility,size,include,cor,0.6,NA,NA,NA,NA,NA,NA,NA,NA,predictable_fluctuating_test_on_unpredictable_fluctuating,table 2,fertility,size,genotype,0.693147181,21,1,0.693147181,female,adult,Insecta,between
1112,Drosophila simulans,167,rayyan-197247019,Few genetic and environmental correlations between life history and stress resistance traits affect adaptation to fluctuating thermal regimes,2016,2012,"Bologna, Italy",lab,female,female,NA,NA,21,21,NA,NA,NA,NA,210,210,line_mean_correlation,genetic_line,yes,broad,authors,adult,adult,productivity,body size (female right wing),fertility,size,include,cor,-0.18,NA,NA,NA,NA,NA,NA,NA,NA,unpredictable_fluctuating_test_on_constant,table 2,fertility,size,genotype,-0.181982689,21,1,-0.181982689,female,adult,Insecta,between
1113,Drosophila simulans,167,rayyan-197247019,Few genetic and environmental correlations between life history and stress resistance traits affect adaptation to fluctuating thermal regimes,2016,2012,"Bologna, Italy",lab,female,female,NA,NA,21,21,NA,NA,NA,NA,210,210,line_mean_correlation,genetic_line,yes,broad,authors,adult,adult,productivity,body size (female right wing),fertility,size,include,cor,-0.31,NA,NA,NA,NA,NA,NA,NA,NA,constant_selection_test_on_predictable_fluctuating,table 2,fertility,size,genotype,-0.320545409,21,1,-0.320545409,female,adult,Insecta,between
1114,Drosophila simulans,167,rayyan-197247019,Few genetic and environmental correlations between life history and stress resistance traits affect adaptation to fluctuating thermal regimes,2016,2012,"Bologna, Italy",lab,female,female,NA,NA,21,21,NA,NA,NA,NA,210,840,line_mean_correlation,genetic_line,yes,broad,authors,adult,non_adult,productivity,developmental time ,fertility,reverse_maturation,include,cor,0.49,NA,NA,NA,NA,NA,NA,NA,NA,constant_selection_test_on_unpredictable_fluctuating,table 2,fertility,maturation,genotype,0.536060337,21,-1,-0.536060337,female,cross,Insecta,between
1115,Drosophila simulans,167,rayyan-197247019,Few genetic and environmental correlations between life history and stress resistance traits affect adaptation to fluctuating thermal regimes,2016,2012,"Bologna, Italy",lab,female,female,NA,NA,21,21,NA,NA,NA,NA,210,840,line_mean_correlation,genetic_line,yes,broad,authors,adult,non_adult,productivity,developmental time ,fertility,reverse_maturation,include,cor,0.23,NA,NA,NA,NA,NA,NA,NA,NA,constant_selection_test_on_predictable_fluctuating,table 2,fertility,maturation,genotype,0.234189467,21,-1,-0.234189467,female,cross,Insecta,between
1116,Drosophila simulans,167,rayyan-197247019,Few genetic and environmental correlations between life history and stress resistance traits affect adaptation to fluctuating thermal regimes,2016,2012,"Bologna, Italy",lab,female,female,NA,NA,21,21,NA,NA,NA,NA,210,840,line_mean_correlation,genetic_line,yes,broad,authors,adult,non_adult,productivity,developmental time ,fertility,reverse_maturation,include,cor,0.37,NA,NA,NA,NA,NA,NA,NA,NA,constant_selection_test_on_constant,table 2,fertility,maturation,genotype,0.3884231,21,-1,-0.3884231,female,cross,Insecta,between
1117,Drosophila simulans,167,rayyan-197247019,Few genetic and environmental correlations between life history and stress resistance traits affect adaptation to fluctuating thermal regimes,2016,2012,"Bologna, Italy",lab,female,both,NA,NA,21,21,NA,NA,NA,NA,210,840,line_mean_correlation,genetic_line,yes,broad,authors,adult,non_adult,body size (female right wing),developmental time ,size,reverse_maturation,include,cor,0.26,NA,NA,NA,NA,NA,NA,NA,NA,constant_selection_test_on_constant,table 2,size,maturation,genotype,0.266108407,21,-1,-0.266108407,female,cross,Insecta,between
1118,Drosophila simulans,167,rayyan-197247019,Few genetic and environmental correlations between life history and stress resistance traits affect adaptation to fluctuating thermal regimes,2016,2012,"Bologna, Italy",lab,female,female,NA,NA,21,21,NA,NA,NA,NA,210,840,line_mean_correlation,genetic_line,yes,broad,authors,adult,non_adult,productivity,developmental time ,fertility,reverse_maturation,include,cor,0.46,NA,NA,NA,NA,NA,NA,NA,NA,predictable_fluctuating_test_on_unpredictable_fluctuating,table 2,fertility,maturation,genotype,0.497311288,21,-1,-0.497311288,female,cross,Insecta,between
1119,Drosophila simulans,167,rayyan-197247019,Few genetic and environmental correlations between life history and stress resistance traits affect adaptation to fluctuating thermal regimes,2016,2012,"Bologna, Italy",lab,female,both,NA,NA,21,21,NA,NA,NA,NA,210,840,line_mean_correlation,genetic_line,yes,broad,authors,adult,non_adult,body size (female right wing),developmental time ,size,reverse_maturation,include,cor,-0.61,NA,NA,NA,NA,NA,NA,NA,NA,predictable_fluctuating_test_on_predictable_fluctuating,table 2,size,maturation,genotype,-0.708921359,21,-1,0.708921359,female,cross,Insecta,between
1120,Drosophila simulans,167,rayyan-197247019,Few genetic and environmental correlations between life history and stress resistance traits affect adaptation to fluctuating thermal regimes,2016,2012,"Bologna, Italy",lab,female,both,NA,NA,21,21,NA,NA,NA,NA,210,840,line_mean_correlation,genetic_line,yes,broad,authors,adult,non_adult,body size (female right wing),developmental time ,size,reverse_maturation,include,cor,0.46,NA,NA,NA,NA,NA,NA,NA,NA,predictable_fluctuating_test_on_unpredictable_fluctuating,table 2,size,maturation,genotype,0.497311288,21,-1,-0.497311288,female,cross,Insecta,between
1121,Drosophila simulans,167,rayyan-197247019,Few genetic and environmental correlations between life history and stress resistance traits affect adaptation to fluctuating thermal regimes,2016,2012,"Bologna, Italy",lab,female,female,NA,NA,21,21,NA,NA,NA,NA,210,840,line_mean_correlation,genetic_line,yes,broad,authors,adult,non_adult,productivity,developmental time ,fertility,reverse_maturation,include,cor,0.34,NA,NA,NA,NA,NA,NA,NA,NA,unpredictable_fluctuating_test_on_predictable_fluctuating,table 2,fertility,maturation,genotype,0.354092529,21,-1,-0.354092529,female,cross,Insecta,between
1122,Drosophila simulans,167,rayyan-197247019,Few genetic and environmental correlations between life history and stress resistance traits affect adaptation to fluctuating thermal regimes,2016,2012,"Bologna, Italy",lab,female,both,NA,NA,21,21,NA,NA,NA,NA,210,840,line_mean_correlation,genetic_line,yes,broad,authors,adult,non_adult,body size (female right wing),developmental time ,size,reverse_maturation,include,cor,0.45,NA,NA,NA,NA,NA,NA,NA,NA,unpredictable_fluctuating_test_on_predictable_fluctuating,table 2,size,maturation,genotype,0.484700279,21,-1,-0.484700279,female,cross,Insecta,between
1123,Drosophila simulans,167,rayyan-197247019,Few genetic and environmental correlations between life history and stress resistance traits affect adaptation to fluctuating thermal regimes,2016,2012,"Bologna, Italy",lab,female,female,NA,NA,21,21,NA,NA,NA,NA,210,210,line_mean_correlation,genetic_line,yes,broad,authors,adult,adult,productivity,body size (female right wing),fertility,size,include,cor,0.7,NA,NA,NA,NA,NA,NA,NA,NA,constant_selection_test_on_unpredictable_fluctuating,table 2,fertility,size,genotype,0.867300528,21,1,0.867300528,female,adult,Insecta,between
1124,Drosophila simulans,167,rayyan-197247019,Few genetic and environmental correlations between life history and stress resistance traits affect adaptation to fluctuating thermal regimes,2016,2012,"Bologna, Italy",lab,female,female,NA,NA,21,21,NA,NA,NA,NA,210,840,line_mean_correlation,genetic_line,yes,broad,authors,adult,non_adult,productivity,developmental time ,fertility,reverse_maturation,include,cor,0.4,NA,NA,NA,NA,NA,NA,NA,NA,predictable_fluctuating_test_on_predictable_fluctuating,table 2,fertility,maturation,genotype,0.42364893,21,-1,-0.42364893,female,cross,Insecta,between
1125,Drosophila simulans,167,rayyan-197247019,Few genetic and environmental correlations between life history and stress resistance traits affect adaptation to fluctuating thermal regimes,2016,2012,"Bologna, Italy",lab,female,female,NA,NA,21,21,NA,NA,NA,NA,210,210,line_mean_correlation,genetic_line,yes,broad,authors,adult,adult,productivity,body size (female right wing),fertility,size,include,cor,0.74,NA,NA,NA,NA,NA,NA,NA,NA,unpredictable_fluctuating_test_on_predictable_fluctuating,table 2,fertility,size,genotype,0.950479381,21,1,0.950479381,female,adult,Insecta,between
1126,Drosophila simulans,167,rayyan-197247019,Few genetic and environmental correlations between life history and stress resistance traits affect adaptation to fluctuating thermal regimes,2016,2012,"Bologna, Italy",lab,female,female,NA,NA,21,21,NA,NA,NA,NA,210,210,line_mean_correlation,genetic_line,yes,broad,authors,adult,adult,productivity,body size (female right wing),fertility,size,include,cor,0.04,NA,NA,NA,NA,NA,NA,NA,NA,constant_selection_test_on_constant,table 2,fertility,size,genotype,0.040021354,21,1,0.040021354,female,adult,Insecta,between
1127,Drosophila simulans,167,rayyan-197247019,Few genetic and environmental correlations between life history and stress resistance traits affect adaptation to fluctuating thermal regimes,2016,2012,"Bologna, Italy",lab,female,both,NA,NA,21,21,NA,NA,NA,NA,210,840,line_mean_correlation,genetic_line,yes,broad,authors,adult,non_adult,body size (female right wing),developmental time ,size,reverse_maturation,include,cor,0.42,NA,NA,NA,NA,NA,NA,NA,NA,constant_selection_test_on_unpredictable_fluctuating,table 2,size,maturation,genotype,0.447692024,21,-1,-0.447692024,female,cross,Insecta,between
1128,Drosophila simulans,167,rayyan-197247019,Few genetic and environmental correlations between life history and stress resistance traits affect adaptation to fluctuating thermal regimes,2016,2012,"Bologna, Italy",lab,female,female,NA,NA,21,21,NA,NA,NA,NA,210,840,line_mean_correlation,genetic_line,yes,broad,authors,adult,non_adult,productivity,developmental time ,fertility,reverse_maturation,include,cor,0.34,NA,NA,NA,NA,NA,NA,NA,NA,unpredictable_fluctuating_test_on_constant,table 2,fertility,maturation,genotype,0.354092529,21,-1,-0.354092529,female,cross,Insecta,between
1129,Drosophila simulans,167,rayyan-197247019,Few genetic and environmental correlations between life history and stress resistance traits affect adaptation to fluctuating thermal regimes,2016,2012,"Bologna, Italy",lab,female,female,NA,NA,21,21,NA,NA,NA,NA,210,210,line_mean_correlation,genetic_line,yes,broad,authors,adult,adult,productivity,body size (female right wing),fertility,size,include,cor,-0.34,NA,NA,NA,NA,NA,NA,NA,NA,predictable_fluctuating_test_on_predictable_fluctuating,table 2,fertility,size,genotype,-0.354092529,21,1,-0.354092529,female,adult,Insecta,between
1130,Drosophila simulans,167,rayyan-197247019,Few genetic and environmental correlations between life history and stress resistance traits affect adaptation to fluctuating thermal regimes,2016,2012,"Bologna, Italy",lab,female,both,NA,NA,21,21,NA,NA,NA,NA,210,840,line_mean_correlation,genetic_line,yes,broad,authors,adult,non_adult,body size (female right wing),developmental time ,size,reverse_maturation,include,cor,-0.08,NA,NA,NA,NA,NA,NA,NA,NA,unpredictable_fluctuating_test_on_constant,table 2,size,maturation,genotype,-0.080171325,21,-1,0.080171325,female,cross,Insecta,between
1131,Drosophila simulans,167,rayyan-197247019,Few genetic and environmental correlations between life history and stress resistance traits affect adaptation to fluctuating thermal regimes,2016,2012,"Bologna, Italy",lab,female,female,NA,NA,21,21,NA,NA,NA,NA,210,840,line_mean_correlation,genetic_line,yes,broad,authors,adult,non_adult,productivity,developmental time ,fertility,reverse_maturation,include,cor,0.07,NA,NA,NA,NA,NA,NA,NA,NA,unpredictable_fluctuating_test_on_predictable_fluctuating,table 2,fertility,maturation,genotype,0.070114671,21,-1,-0.070114671,female,cross,Insecta,between
1132,Drosophila simulans,167,rayyan-197247019,Few genetic and environmental correlations between life history and stress resistance traits affect adaptation to fluctuating thermal regimes,2016,2012,"Bologna, Italy",lab,female,both,NA,NA,21,21,NA,NA,NA,NA,210,840,line_mean_correlation,genetic_line,yes,broad,authors,adult,non_adult,body size (female right wing),developmental time ,size,reverse_maturation,include,cor,0.31,NA,NA,NA,NA,NA,NA,NA,NA,predictable_fluctuating_test_on_constant,table 2,size,maturation,genotype,0.320545409,21,-1,-0.320545409,female,cross,Insecta,between
1133,Drosophila simulans,167,rayyan-197247019,Few genetic and environmental correlations between life history and stress resistance traits affect adaptation to fluctuating thermal regimes,2016,2012,"Bologna, Italy",lab,female,female,NA,NA,21,21,NA,NA,NA,NA,210,840,line_mean_correlation,genetic_line,yes,broad,authors,adult,non_adult,productivity,developmental time ,fertility,reverse_maturation,include,cor,0.27,NA,NA,NA,NA,NA,NA,NA,NA,predictable_fluctuating_test_on_constant,table 2,fertility,maturation,genotype,0.276863823,21,-1,-0.276863823,female,cross,Insecta,between
1134,Drosophila simulans,167,rayyan-197247019,Few genetic and environmental correlations between life history and stress resistance traits affect adaptation to fluctuating thermal regimes,2016,2012,"Bologna, Italy",lab,female,both,NA,NA,21,21,NA,NA,NA,NA,210,840,line_mean_correlation,genetic_line,yes,broad,authors,adult,non_adult,body size (female right wing),developmental time ,size,reverse_maturation,include,cor,-0.41,NA,NA,NA,NA,NA,NA,NA,NA,unpredictable_fluctuating_test_on_predictable_fluctuating,table 2,size,maturation,genotype,-0.435611223,21,-1,0.435611223,female,cross,Insecta,between
1135,Drosophila simulans,167,rayyan-197247019,Few genetic and environmental correlations between life history and stress resistance traits affect adaptation to fluctuating thermal regimes,2016,2012,"Bologna, Italy",lab,female,female,NA,NA,21,21,NA,NA,NA,NA,210,210,line_mean_correlation,genetic_line,yes,broad,authors,adult,adult,productivity,body size (female right wing),fertility,size,include,cor,-0.45,NA,NA,NA,NA,NA,NA,NA,NA,unpredictable_fluctuating_test_on_predictable_fluctuating,table 2,fertility,size,genotype,-0.484700279,21,1,-0.484700279,female,adult,Insecta,between
1136,Drosophila simulans,167,rayyan-197247019,Few genetic and environmental correlations between life history and stress resistance traits affect adaptation to fluctuating thermal regimes,2016,2012,"Bologna, Italy",lab,female,female,NA,NA,21,21,NA,NA,NA,NA,210,210,line_mean_correlation,genetic_line,yes,broad,authors,adult,adult,productivity,body size (female right wing),fertility,size,include,cor,0.09,NA,NA,NA,NA,NA,NA,NA,NA,predictable_fluctuating_test_on_constant,table 2,fertility,size,genotype,0.090244188,21,1,0.090244188,female,adult,Insecta,between
1137,Drosophila subobscura,8,rayyan-178530585,Adaptation to the laboratory environment in Drosophila subobscura,2000,1990-1992,"Sintra, Portugal",lab,female,female,NA,NA,NA,NA,307,307,52,52,374,375,animal_model,half_sib,no,narrow,authors,adult,adult,total egg laying,mean egg laying daily,fertility,fertility,include,cor,0.868571429,0.142857143,se,NA,NA,NA,NA,NA,NA,gen29,figure 2c,fertility,fertility,family,1.327232979,307,1,1.327232979,female,adult,Insecta,within
1138,Drosophila subobscura,8,rayyan-178530585,Adaptation to the laboratory environment in Drosophila subobscura,2000,1990-1992,"Sintra, Portugal",lab,female,female,NA,NA,NA,NA,168,168,56,56,235,374,animal_model,half_sib,no,narrow,authors,adult,adult,total egg laying in the first week of life,mean egg laying daily,fertility,fertility,include,cor,0.982857143,0.188571429,se,NA,NA,NA,NA,NA,NA,gen2,figure 2c,fertility,fertility,family,2.37535625,168,1,2.37535625,female,adult,Insecta,within
1139,Drosophila subobscura,8,rayyan-178530585,Adaptation to the laboratory environment in Drosophila subobscura,2000,1990-1992,"Sintra, Portugal",lab,female,female,NA,NA,NA,NA,308,308,52,52,375,376,animal_model,half_sib,no,narrow,authors,adult,adult,total egg laying,mean egg laying daily,fertility,fertility,include,cor,0.462857143,0.308571429,se,NA,NA,NA,NA,NA,NA,gen25,figure 2c,fertility,fertility,family,0.500941331,308,1,0.500941331,female,adult,Insecta,within
1140,Drosophila subobscura,8,rayyan-178530585,Adaptation to the laboratory environment in Drosophila subobscura,2000,1990-1992,"Sintra, Portugal",lab,female,female,NA,NA,NA,NA,309,309,52,52,370,335,animal_model,half_sib,no,narrow,authors,adult,adult,total egg laying in the sixth week of life,total egg laying,fertility,fertility,include,cor,0.828272251,0.183769634,se,NA,NA,NA,NA,NA,NA,gen19,figure 2d,fertility,fertility,family,1.182608153,309,1,1.182608153,female,adult,Insecta,within
1141,Drosophila subobscura,8,rayyan-178530585,Adaptation to the laboratory environment in Drosophila subobscura,2000,1990-1992,"Sintra, Portugal",lab,female,female,NA,NA,NA,NA,308,308,52,52,344,376,animal_model,half_sib,no,narrow,authors,adult,adult,total egg laying in the sixth week of life,total egg laying,fertility,fertility,include,cor,0.828272251,0.136125654,se,NA,NA,NA,NA,NA,NA,gen25,figure 2d,fertility,fertility,family,1.182608153,308,1,1.182608153,female,adult,Insecta,within
1142,Drosophila subobscura,8,rayyan-178530585,Adaptation to the laboratory environment in Drosophila subobscura,2000,1990-1992,"Sintra, Portugal",lab,female,female,NA,NA,NA,NA,293,293,52,52,360,235,animal_model,half_sib,no,narrow,authors,adult,adult,total egg laying in the first week of life,mean egg laying daily,fertility,fertility,include,cor,0.028571429,0.382857143,se,NA,NA,NA,NA,NA,NA,gen10,figure 2c,fertility,fertility,family,0.028579207,293,1,0.028579207,female,adult,Insecta,within
1143,Drosophila subobscura,8,rayyan-178530585,Adaptation to the laboratory environment in Drosophila subobscura,2000,1990-1992,"Sintra, Portugal",lab,female,female,NA,NA,NA,NA,268,268,52,52,335,360,animal_model,half_sib,no,narrow,authors,adult,adult,total egg laying in the first week of life,mean egg laying daily,fertility,fertility,include,cor,0.685714286,0.32,se,NA,NA,NA,NA,NA,NA,gen15,figure 2c,fertility,fertility,family,0.839821086,268,1,0.839821086,female,adult,Insecta,within
1144,Drosophila subobscura,8,rayyan-178530585,Adaptation to the laboratory environment in Drosophila subobscura,2000,1990-1992,"Sintra, Portugal",lab,female,female,NA,NA,NA,NA,309,309,52,52,376,335,animal_model,half_sib,no,narrow,authors,adult,adult,total egg laying in the first week of life,mean egg laying daily,fertility,fertility,include,cor,0.485714286,0.217142857,se,NA,NA,NA,NA,NA,NA,gen19,figure 2c,fertility,fertility,family,0.530435981,309,1,0.530435981,female,adult,Insecta,within
1145,Drosophila subobscura,8,rayyan-178530585,Adaptation to the laboratory environment in Drosophila subobscura,2000,1990-1992,"Sintra, Portugal",lab,female,female,NA,NA,NA,NA,307,307,52,52,302,375,animal_model,half_sib,no,narrow,authors,adult,adult,total egg laying in the sixth week of life,total egg laying,fertility,fertility,include,cor,0.978010471,0.258638743,se,NA,NA,NA,NA,NA,NA,gen29,figure 2d,fertility,fertility,family,2.24964021,307,1,2.24964021,female,adult,Insecta,within
1146,Drosophila subobscura,8,rayyan-178530585,Adaptation to the laboratory environment in Drosophila subobscura,2000,1990-1992,"Sintra, Portugal",lab,female,female,NA,NA,NA,NA,276,276,51,51,342,235,animal_model,half_sib,no,narrow,authors,adult,non_adult,total egg laying in the first week of life,time of development (emergence),fertility,reverse_maturation,include,cor,0.386666667,0.246666667,se,NA,NA,NA,NA,NA,NA,gen6,figure 2e,fertility,maturation,family,0.407874752,276,-1,-0.407874752,female,cross,Insecta,between
1147,Drosophila subobscura,8,rayyan-178530585,Adaptation to the laboratory environment in Drosophila subobscura,2000,1990-1992,"Sintra, Portugal",lab,female,female,NA,NA,NA,NA,268,268,52,52,301,360,animal_model,half_sib,no,narrow,authors,adult,adult,total egg laying in the sixth week of life,total egg laying,fertility,fertility,include,cor,0.556020942,0.204188482,se,NA,NA,NA,NA,NA,NA,gen15,figure 2d,fertility,fertility,family,0.627054884,268,1,0.627054884,female,adult,Insecta,within
1148,Drosophila subobscura,8,rayyan-178530585,Adaptation to the laboratory environment in Drosophila subobscura,2000,1990-1992,"Sintra, Portugal",lab,female,female,NA,NA,NA,NA,268,268,52,52,335,360,animal_model,half_sib,no,narrow,authors,adult,non_adult,total egg laying in the first week of life,time of development (emergence),fertility,reverse_maturation,include,cor,0.253333333,0.326666667,se,NA,NA,NA,NA,NA,NA,gen15,figure 2e,fertility,maturation,family,0.258971545,268,-1,-0.258971545,female,cross,Insecta,between
1149,Drosophila subobscura,8,rayyan-178530585,Adaptation to the laboratory environment in Drosophila subobscura,2000,1990-1992,"Sintra, Portugal",lab,female,female,NA,NA,NA,NA,268,268,52,52,335,360,animal_model,half_sib,no,narrow,authors,adult,adult,total egg laying in the third week of life,total egg laying,fertility,fertility,include,cor,-0.927748691,0.503664921,se,NA,NA,NA,NA,NA,NA,gen15,figure 2d,fertility,fertility,family,-1.641978838,268,1,-1.641978838,female,adult,Insecta,within
1150,Drosophila subobscura,8,rayyan-178530585,Adaptation to the laboratory environment in Drosophila subobscura,2000,1990-1992,"Sintra, Portugal",lab,female,female,NA,NA,NA,NA,308,308,52,52,375,376,animal_model,half_sib,no,narrow,authors,adult,non_adult,total egg laying in the first week of life,time of development (emergence),fertility,reverse_maturation,include,cor,0.353333333,0.226666667,se,NA,NA,NA,NA,NA,NA,gen25,figure 2e,fertility,maturation,family,0.3692475,308,-1,-0.3692475,female,cross,Insecta,between
1151,Drosophila subobscura,8,rayyan-178530585,Adaptation to the laboratory environment in Drosophila subobscura,2000,1990-1992,"Sintra, Portugal",lab,female,female,NA,NA,NA,NA,308,308,52,52,375,344,animal_model,half_sib,no,narrow,authors,adult,adult,total egg laying in the third week of life,total egg laying in the sixth week of life,fertility,fertility,include,cor,0.564456233,0.373474801,se,NA,NA,NA,NA,NA,NA,gen25,figure 2a,fertility,fertility,family,0.639349149,308,1,0.639349149,female,adult,Insecta,within
1152,Drosophila subobscura,8,rayyan-178530585,Adaptation to the laboratory environment in Drosophila subobscura,2000,1990-1992,"Sintra, Portugal",lab,female,female,NA,NA,NA,NA,307,307,52,52,374,302,animal_model,half_sib,no,narrow,authors,adult,adult,total egg laying in the third week of life,total egg laying in the sixth week of life,fertility,fertility,include,cor,NA,0.407427056,se,NA,NA,NA,NA,NA,NA,gen29,figure 2a,fertility,fertility,family,NA,307,1,NA,female,adult,Insecta,within
1153,Drosophila subobscura,8,rayyan-178530585,Adaptation to the laboratory environment in Drosophila subobscura,2000,1990-1992,"Sintra, Portugal",lab,female,female,NA,NA,NA,NA,309,309,52,52,376,335,animal_model,half_sib,no,narrow,authors,adult,non_adult,total egg laying in the first week of life,time of development (emergence),fertility,reverse_maturation,include,cor,0.6,0.286666667,se,NA,NA,NA,NA,NA,NA,gen19,figure 2e,fertility,maturation,family,0.693147181,309,-1,-0.693147181,female,cross,Insecta,between
1154,Drosophila subobscura,8,rayyan-178530585,Adaptation to the laboratory environment in Drosophila subobscura,2000,1990-1992,"Sintra, Portugal",lab,female,female,NA,NA,NA,NA,293,293,52,52,360,342,animal_model,half_sib,no,narrow,authors,adult,both,total egg laying in the third week of life,longevity,fertility,survival,include,cor,0.199469496,0.492307692,se,NA,NA,NA,NA,NA,NA,gen10,figure 2a,fertility,survival,family,0.202180007,293,1,0.202180007,female,cross,Insecta,between
1155,Drosophila subobscura,8,rayyan-178530585,Adaptation to the laboratory environment in Drosophila subobscura,2000,1990-1992,"Sintra, Portugal",lab,female,female,NA,NA,NA,NA,309,309,52,52,376,335,animal_model,half_sib,no,narrow,authors,adult,adult,total egg laying in the third week of life,total egg laying,fertility,fertility,include,cor,0.807853403,0.183769634,se,NA,NA,NA,NA,NA,NA,gen19,figure 2d,fertility,fertility,family,1.120818424,309,1,1.120818424,female,adult,Insecta,within
1156,Drosophila subobscura,8,rayyan-178530585,Adaptation to the laboratory environment in Drosophila subobscura,2000,1990-1992,"Sintra, Portugal",lab,female,female,NA,NA,NA,NA,308,308,52,52,375,376,animal_model,half_sib,no,narrow,authors,adult,adult,total egg laying in the third week of life,total egg laying,fertility,fertility,include,cor,0.576439791,0.204188482,se,NA,NA,NA,NA,NA,NA,gen25,figure 2d,fertility,fertility,family,0.657114306,308,1,0.657114306,female,adult,Insecta,within
1157,Drosophila subobscura,8,rayyan-178530585,Adaptation to the laboratory environment in Drosophila subobscura,2000,1990-1992,"Sintra, Portugal",lab,female,female,NA,NA,NA,NA,276,276,51,51,342,322,animal_model,half_sib,no,narrow,authors,adult,both,total egg laying in the third week of life,longevity,fertility,survival,include,cor,0.81061008,0.611140584,se,NA,NA,NA,NA,NA,NA,gen6,figure 2a,fertility,survival,family,1.128805585,276,1,1.128805585,female,cross,Insecta,between
1158,Drosophila subobscura,8,rayyan-178530585,Adaptation to the laboratory environment in Drosophila subobscura,2000,1990-1992,"Sintra, Portugal",lab,female,female,NA,NA,NA,NA,168,168,56,56,235,374,animal_model,half_sib,no,narrow,authors,adult,non_adult,total egg laying in the first week of life,time of development (emergence),fertility,reverse_maturation,include,cor,0.253333333,0.173333333,se,NA,NA,NA,NA,NA,NA,gen2,figure 2e,fertility,maturation,family,0.258971545,168,-1,-0.258971545,female,cross,Insecta,between
1159,Drosophila subobscura,8,rayyan-178530585,Adaptation to the laboratory environment in Drosophila subobscura,2000,1990-1992,"Sintra, Portugal",lab,female,female,NA,NA,NA,NA,293,293,52,52,360,342,animal_model,half_sib,no,narrow,authors,adult,adult,total egg laying in the first week of life,total egg laying,fertility,fertility,include,cor,-0.002094241,0.428795812,se,NA,NA,NA,NA,NA,NA,gen10,figure 2d,fertility,fertility,family,-0.002094244,293,1,-0.002094244,female,adult,Insecta,within
1160,Drosophila subobscura,8,rayyan-178530585,Adaptation to the laboratory environment in Drosophila subobscura,2000,1990-1992,"Sintra, Portugal",lab,female,female,NA,NA,NA,NA,293,293,52,52,360,342,animal_model,half_sib,no,narrow,authors,adult,non_adult,total egg laying in the first week of life,time of development (emergence),fertility,reverse_maturation,include,cor,0.793333333,0.413333333,se,NA,NA,NA,NA,NA,NA,gen10,figure 2e,fertility,maturation,family,1.080362087,293,-1,-1.080362087,female,cross,Insecta,between
1161,Drosophila subobscura,8,rayyan-178530585,Adaptation to the laboratory environment in Drosophila subobscura,2000,1990-1992,"Sintra, Portugal",lab,female,female,NA,NA,NA,NA,309,309,52,52,376,335,animal_model,half_sib,no,narrow,authors,adult,adult,total egg laying in the first week of life,total egg laying,fertility,fertility,include,cor,0.54921466,0.251832461,se,NA,NA,NA,NA,NA,NA,gen19,figure 2d,fertility,fertility,family,0.617256074,309,1,0.617256074,female,adult,Insecta,within
1162,Drosophila subobscura,8,rayyan-178530585,Adaptation to the laboratory environment in Drosophila subobscura,2000,1990-1992,"Sintra, Portugal",lab,female,female,NA,NA,NA,NA,308,308,52,52,375,376,animal_model,half_sib,no,narrow,authors,adult,adult,total egg laying in the first week of life,total egg laying,fertility,fertility,include,cor,0.134031414,0.319895288,se,NA,NA,NA,NA,NA,NA,gen25,figure 2d,fertility,fertility,family,0.134842776,308,1,0.134842776,female,adult,Insecta,within
1163,Drosophila subobscura,8,rayyan-178530585,Adaptation to the laboratory environment in Drosophila subobscura,2000,1990-1992,"Sintra, Portugal",lab,female,female,NA,NA,NA,NA,307,307,52,52,374,375,animal_model,half_sib,no,narrow,authors,adult,adult,total egg laying in the first week of life,total egg laying,fertility,fertility,include,cor,0.671727749,0.088481675,se,NA,NA,NA,NA,NA,NA,gen29,figure 2d,fertility,fertility,family,0.813884827,307,1,0.813884827,female,adult,Insecta,within
1164,Drosophila subobscura,8,rayyan-178530585,Adaptation to the laboratory environment in Drosophila subobscura,2000,1990-1992,"Sintra, Portugal",lab,female,female,NA,NA,NA,NA,168,168,56,56,235,374,animal_model,half_sib,no,narrow,authors,both,adult,longevity,total egg laying,survival,fertility,include,cor,0.794240838,0.129319372,se,NA,NA,NA,NA,NA,NA,gen2,figure 2d,survival,fertility,family,1.082815456,168,1,1.082815456,female,cross,Insecta,between
1165,Drosophila subobscura,8,rayyan-178530585,Adaptation to the laboratory environment in Drosophila subobscura,2000,1990-1992,"Sintra, Portugal",lab,female,female,NA,NA,NA,NA,276,276,51,51,342,235,animal_model,half_sib,no,narrow,authors,both,adult,longevity,total egg laying,survival,fertility,include,cor,NA,0.210994764,se,NA,NA,NA,NA,NA,NA,gen6,figure 2d,survival,fertility,family,NA,276,1,NA,female,cross,Insecta,between
1166,Drosophila subobscura,8,rayyan-178530585,Adaptation to the laboratory environment in Drosophila subobscura,2000,1990-1992,"Sintra, Portugal",lab,female,female,NA,NA,NA,NA,293,293,52,52,360,342,animal_model,half_sib,no,narrow,authors,both,adult,longevity,total egg laying,survival,fertility,include,cor,0.753403141,0.156544503,se,NA,NA,NA,NA,NA,NA,gen10,figure 2d,survival,fertility,family,0.980779489,293,1,0.980779489,female,cross,Insecta,between
1167,Drosophila subobscura,8,rayyan-178530585,Adaptation to the laboratory environment in Drosophila subobscura,2000,1990-1992,"Sintra, Portugal",lab,female,female,NA,NA,NA,NA,268,268,52,52,335,360,animal_model,half_sib,no,narrow,authors,both,adult,longevity,total egg laying,survival,fertility,include,cor,0.916753927,0.088481675,se,NA,NA,NA,NA,NA,NA,gen15,figure 2d,survival,fertility,family,1.568293707,268,1,1.568293707,female,cross,Insecta,between
1168,Drosophila subobscura,8,rayyan-178530585,Adaptation to the laboratory environment in Drosophila subobscura,2000,1990-1992,"Sintra, Portugal",lab,female,female,NA,NA,NA,NA,308,308,52,52,375,376,animal_model,half_sib,no,narrow,authors,adult,adult,total egg laying in the first week of life,mean egg laying daily,fertility,fertility,include,cor,0.554285714,0.268571429,se,NA,NA,NA,NA,NA,NA,gen25,figure 2c,fertility,fertility,family,0.624546619,308,1,0.624546619,female,adult,Insecta,within
1169,Drosophila subobscura,8,rayyan-178530585,Adaptation to the laboratory environment in Drosophila subobscura,2000,1990-1992,"Sintra, Portugal",lab,female,female,NA,NA,NA,NA,307,307,52,52,374,375,animal_model,half_sib,no,narrow,authors,adult,adult,total egg laying in the first week of life,mean egg laying daily,fertility,fertility,include,cor,0.685714286,0.188571429,se,NA,NA,NA,NA,NA,NA,gen29,figure 2c,fertility,fertility,family,0.839821086,307,1,0.839821086,female,adult,Insecta,within
1170,Drosophila subobscura,8,rayyan-178530585,Adaptation to the laboratory environment in Drosophila subobscura,2000,1990-1992,"Sintra, Portugal",lab,female,female,NA,NA,NA,NA,307,307,52,52,374,375,animal_model,half_sib,no,narrow,authors,adult,adult,total egg laying in the third week of life,total egg laying,fertility,fertility,include,cor,0.971204188,0.156544503,se,NA,NA,NA,NA,NA,NA,gen29,figure 2d,fertility,fertility,family,2.113084969,307,1,2.113084969,female,adult,Insecta,within
1171,Drosophila subobscura,8,rayyan-178530585,Adaptation to the laboratory environment in Drosophila subobscura,2000,1990-1992,"Sintra, Portugal",lab,female,female,NA,NA,NA,NA,276,276,51,51,342,235,animal_model,half_sib,no,narrow,authors,adult,adult,total egg laying in the first week of life,total egg laying,fertility,fertility,include,cor,0.154450262,0.265445026,se,NA,NA,NA,NA,NA,NA,gen6,figure 2d,fertility,fertility,family,0.155696276,276,1,0.155696276,female,adult,Insecta,within
1172,Drosophila subobscura,8,rayyan-178530585,Adaptation to the laboratory environment in Drosophila subobscura,2000,1990-1992,"Sintra, Portugal",lab,female,female,NA,NA,NA,NA,276,276,51,51,322,235,animal_model,half_sib,no,narrow,authors,adult,adult,total egg laying in the sixth week of life,total egg laying,fertility,fertility,include,cor,0.794240838,0.306282723,se,NA,NA,NA,NA,NA,NA,gen6,figure 2d,fertility,fertility,family,1.082815456,276,1,1.082815456,female,adult,Insecta,within
1173,Drosophila subobscura,8,rayyan-178530585,Adaptation to the laboratory environment in Drosophila subobscura,2000,1990-1992,"Sintra, Portugal",lab,female,female,NA,NA,NA,NA,268,268,52,52,335,360,animal_model,half_sib,no,narrow,authors,adult,adult,total egg laying in the first week of life,total egg laying,fertility,fertility,include,cor,-0.008900524,0.333507853,se,NA,NA,NA,NA,NA,NA,gen15,figure 2d,fertility,fertility,family,-0.008900759,268,1,-0.008900759,female,adult,Insecta,within
1174,Drosophila subobscura,8,rayyan-178530585,Adaptation to the laboratory environment in Drosophila subobscura,2000,1990-1992,"Sintra, Portugal",lab,female,female,NA,NA,NA,NA,276,276,51,51,342,235,animal_model,half_sib,no,narrow,authors,adult,non_adult,thorax length,time of development (emergence),size,reverse_maturation,include,cor,0.092783505,0.391237113,se,NA,NA,NA,NA,NA,NA,gen6,figure 2b,size,maturation,family,0.09305114,276,-1,-0.09305114,female,cross,Insecta,between
1175,Drosophila subobscura,8,rayyan-178530585,Adaptation to the laboratory environment in Drosophila subobscura,2000,1990-1992,"Sintra, Portugal",lab,female,female,NA,NA,NA,NA,276,276,51,51,342,322,animal_model,half_sib,no,narrow,authors,adult,adult,total egg laying in the first week of life,total egg laying in the sixth week of life,fertility,fertility,include,cor,-0.326790451,0.34801061,se,NA,NA,NA,NA,NA,NA,gen6,figure 2a,fertility,fertility,family,-0.339230732,276,1,-0.339230732,female,adult,Insecta,within
1176,Drosophila subobscura,8,rayyan-178530585,Adaptation to the laboratory environment in Drosophila subobscura,2000,1990-1992,"Sintra, Portugal",lab,female,female,NA,NA,NA,NA,293,293,52,52,360,342,animal_model,half_sib,no,narrow,authors,adult,non_adult,thorax length,time of development (emergence),size,reverse_maturation,include,cor,-0.445876289,0.538659794,se,NA,NA,NA,NA,NA,NA,gen10,figure 2b,size,maturation,family,-0.479541439,293,-1,0.479541439,female,cross,Insecta,between
1177,Drosophila subobscura,8,rayyan-178530585,Adaptation to the laboratory environment in Drosophila subobscura,2000,1990-1992,"Sintra, Portugal",lab,female,female,NA,NA,NA,NA,268,268,52,52,335,360,animal_model,half_sib,no,narrow,authors,adult,non_adult,thorax length,time of development (emergence),size,reverse_maturation,include,cor,0.461340206,0.362886598,se,NA,NA,NA,NA,NA,NA,gen15,figure 2b,size,maturation,family,0.499012526,268,-1,-0.499012526,female,cross,Insecta,between
1178,Drosophila subobscura,8,rayyan-178530585,Adaptation to the laboratory environment in Drosophila subobscura,2000,1990-1992,"Sintra, Portugal",lab,female,female,NA,NA,NA,NA,168,168,56,56,235,374,animal_model,half_sib,no,narrow,authors,adult,adult,total egg laying in the third week of life,total egg laying,fertility,fertility,include,cor,NA,0.163350785,se,NA,NA,NA,NA,NA,NA,gen2,figure 2d,fertility,fertility,family,NA,168,1,NA,female,adult,Insecta,within
1179,Drosophila subobscura,8,rayyan-178530585,Adaptation to the laboratory environment in Drosophila subobscura,2000,1990-1992,"Sintra, Portugal",lab,female,female,NA,NA,NA,NA,276,276,51,51,342,235,animal_model,half_sib,no,narrow,authors,adult,adult,total egg laying in the third week of life,total egg laying,fertility,fertility,include,cor,0.671727749,0.428795812,se,NA,NA,NA,NA,NA,NA,gen6,figure 2d,fertility,fertility,family,0.813884827,276,1,0.813884827,female,adult,Insecta,within
1180,Drosophila subobscura,8,rayyan-178530585,Adaptation to the laboratory environment in Drosophila subobscura,2000,1990-1992,"Sintra, Portugal",lab,female,female,NA,NA,NA,NA,293,293,52,52,360,342,animal_model,half_sib,no,narrow,authors,adult,adult,total egg laying in the third week of life,total egg laying,fertility,fertility,include,cor,NA,0.319895288,se,NA,NA,NA,NA,NA,NA,gen10,figure 2d,fertility,fertility,family,NA,293,1,NA,female,adult,Insecta,within
1181,Drosophila subobscura,8,rayyan-178530585,Adaptation to the laboratory environment in Drosophila subobscura,2000,1990-1992,"Sintra, Portugal",lab,female,female,NA,NA,NA,NA,168,168,56,56,235,374,animal_model,half_sib,no,narrow,authors,both,adult,longevity,mean egg laying daily,survival,fertility,include,cor,0.125714286,0.348571429,se,NA,NA,NA,NA,NA,NA,gen2,figure 2c,survival,fertility,family,0.126382904,168,1,0.126382904,female,cross,Insecta,between
1182,Drosophila subobscura,8,rayyan-178530585,Adaptation to the laboratory environment in Drosophila subobscura,2000,1990-1992,"Sintra, Portugal",lab,female,female,NA,NA,NA,NA,293,293,52,52,360,235,animal_model,half_sib,no,narrow,authors,both,adult,longevity,mean egg laying daily,survival,fertility,include,cor,-0.171428571,0.365714286,se,NA,NA,NA,NA,NA,NA,gen9,figure 2c,survival,fertility,family,-0.173138118,293,1,-0.173138118,female,cross,Insecta,between
1183,Drosophila subobscura,8,rayyan-178530585,Adaptation to the laboratory environment in Drosophila subobscura,2000,1990-1992,"Sintra, Portugal",lab,female,female,NA,NA,NA,NA,168,168,56,56,235,374,animal_model,half_sib,no,narrow,authors,adult,adult,total egg laying in the first week of life,total egg laying,fertility,fertility,include,cor,0.535602094,0.258638743,se,NA,NA,NA,NA,NA,NA,gen2,figure 2d,fertility,fertility,family,0.597968043,168,1,0.597968043,female,adult,Insecta,within
1184,Drosophila subobscura,8,rayyan-178530585,Adaptation to the laboratory environment in Drosophila subobscura,2000,1990-1992,"Sintra, Portugal",lab,female,female,NA,NA,NA,NA,168,168,56,56,235,374,animal_model,half_sib,no,narrow,authors,adult,adult,total egg laying in the sixth week of life,total egg laying,fertility,fertility,include,cor,NA,0.108900524,se,NA,NA,NA,NA,NA,NA,gen2,figure 2d,fertility,fertility,family,NA,168,1,NA,female,adult,Insecta,within
1185,Drosophila subobscura,8,rayyan-178530585,Adaptation to the laboratory environment in Drosophila subobscura,2000,1990-1992,"Sintra, Portugal",lab,female,female,NA,NA,NA,NA,308,308,52,52,375,376,animal_model,half_sib,no,narrow,authors,both,adult,longevity,mean egg laying daily,survival,fertility,include,cor,-0.24,0.417142857,se,NA,NA,NA,NA,NA,NA,gen25,figure 2c,survival,fertility,family,-0.244774113,308,1,-0.244774113,female,cross,Insecta,between
1186,Drosophila subobscura,8,rayyan-178530585,Adaptation to the laboratory environment in Drosophila subobscura,2000,1990-1992,"Sintra, Portugal",lab,female,female,NA,NA,NA,NA,307,307,52,52,374,375,animal_model,half_sib,no,narrow,authors,both,adult,longevity,mean egg laying daily,survival,fertility,include,cor,-0.525714286,0.565714286,se,NA,NA,NA,NA,NA,NA,gen29,figure 2c,survival,fertility,family,-0.584204026,307,1,-0.584204026,female,cross,Insecta,between
1187,Drosophila subobscura,8,rayyan-178530585,Adaptation to the laboratory environment in Drosophila subobscura,2000,1990-1992,"Sintra, Portugal",lab,female,female,NA,NA,NA,NA,168,168,56,56,235,374,animal_model,half_sib,no,narrow,authors,adult,adult,total egg laying,mean egg laying daily,fertility,fertility,include,cor,0.708571429,0.171428571,se,NA,NA,NA,NA,NA,NA,gen2,figure 2c,fertility,fertility,family,0.884308971,168,1,0.884308971,female,adult,Insecta,within
1188,Drosophila subobscura,8,rayyan-178530585,Adaptation to the laboratory environment in Drosophila subobscura,2000,1990-1992,"Sintra, Portugal",lab,female,female,NA,NA,NA,NA,293,293,52,52,360,235,animal_model,half_sib,no,narrow,authors,adult,adult,total egg laying,mean egg laying daily,fertility,fertility,include,cor,0.611428571,0.262857143,se,NA,NA,NA,NA,NA,NA,gen9,figure 2c,fertility,fertility,family,0.711199682,293,1,0.711199682,female,adult,Insecta,within
1189,Drosophila subobscura,8,rayyan-178530585,Adaptation to the laboratory environment in Drosophila subobscura,2000,1990-1992,"Sintra, Portugal",lab,female,female,NA,NA,NA,NA,268,268,52,52,335,360,animal_model,half_sib,no,narrow,authors,adult,adult,total egg laying,mean egg laying daily,fertility,fertility,include,cor,-0.588571429,0.36,se,NA,NA,NA,NA,NA,NA,gen15,figure 2c,fertility,fertility,family,-0.675477498,268,1,-0.675477498,female,adult,Insecta,within
1190,Drosophila subobscura,8,rayyan-178530585,Adaptation to the laboratory environment in Drosophila subobscura,2000,1990-1992,"Sintra, Portugal",lab,female,female,NA,NA,NA,NA,309,309,52,52,376,335,animal_model,half_sib,no,narrow,authors,adult,adult,total egg laying,mean egg laying daily,fertility,fertility,include,cor,0.582857143,0.211428571,se,NA,NA,NA,NA,NA,NA,gen19,figure 2c,fertility,fertility,family,0.666779033,309,1,0.666779033,female,adult,Insecta,within
1191,Drosophila subobscura,8,rayyan-178530585,Adaptation to the laboratory environment in Drosophila subobscura,2000,1990-1992,"Sintra, Portugal",lab,female,female,NA,NA,NA,NA,309,309,52,52,376,370,animal_model,half_sib,no,narrow,authors,adult,adult,total egg laying in the third week of life,total egg laying in the sixth week of life,fertility,fertility,include,cor,0.759681698,0.297082228,se,NA,NA,NA,NA,NA,NA,gen19,figure 2a,fertility,fertility,family,0.995461958,309,1,0.995461958,female,adult,Insecta,within
1192,Drosophila subobscura,8,rayyan-178530585,Adaptation to the laboratory environment in Drosophila subobscura,2000,1990-1992,"Sintra, Portugal",lab,female,female,NA,NA,NA,NA,307,307,52,52,374,375,animal_model,half_sib,no,narrow,authors,adult,non_adult,total egg laying in the first week of life,time of development (emergence),fertility,reverse_maturation,include,cor,-0.086666667,0.266666667,se,NA,NA,NA,NA,NA,NA,gen29,figure 2e,fertility,maturation,family,-0.086884638,307,-1,0.086884638,female,cross,Insecta,between
1193,Drosophila subobscura,8,rayyan-178530585,Adaptation to the laboratory environment in Drosophila subobscura,2000,1990-1992,"Sintra, Portugal",lab,female,female,NA,NA,NA,NA,276,276,51,51,342,374,animal_model,half_sib,no,narrow,authors,adult,non_adult,total egg laying in the third week of life,time of development (emergence),fertility,reverse_maturation,include,cor,-0.566666667,0.353333333,se,NA,NA,NA,NA,NA,NA,gen6,figure 2e,fertility,maturation,family,-0.642599123,276,-1,0.642599123,female,cross,Insecta,between
1194,Drosophila subobscura,8,rayyan-178530585,Adaptation to the laboratory environment in Drosophila subobscura,2000,1990-1992,"Sintra, Portugal",lab,female,female,NA,NA,NA,NA,293,293,52,52,360,342,animal_model,half_sib,no,narrow,authors,adult,non_adult,total egg laying in the third week of life,time of development (emergence),fertility,reverse_maturation,include,cor,-0.72,0.486666667,se,NA,NA,NA,NA,NA,NA,gen10,figure 2e,fertility,maturation,family,-0.907644983,293,-1,0.907644983,female,cross,Insecta,between
1195,Drosophila subobscura,8,rayyan-178530585,Adaptation to the laboratory environment in Drosophila subobscura,2000,1990-1992,"Sintra, Portugal",lab,female,female,NA,NA,NA,NA,268,268,52,52,335,360,animal_model,half_sib,no,narrow,authors,adult,both,total egg laying in the third week of life,longevity,fertility,survival,include,cor,-0.988859416,0.373474801,se,NA,NA,NA,NA,NA,NA,gen15,figure 2a,fertility,survival,family,-2.592360969,268,1,-2.592360969,female,cross,Insecta,between
1196,Drosophila subobscura,8,rayyan-178530585,Adaptation to the laboratory environment in Drosophila subobscura,2000,1990-1992,"Sintra, Portugal",lab,female,female,NA,NA,NA,NA,268,268,52,52,335,360,animal_model,half_sib,no,narrow,authors,both,adult,longevity,mean egg laying daily,survival,fertility,include,cor,-0.902857143,0.16,se,NA,NA,NA,NA,NA,NA,gen15,figure 2c,survival,fertility,family,-1.487464574,268,1,-1.487464574,female,cross,Insecta,between
1197,Drosophila subobscura,8,rayyan-178530585,Adaptation to the laboratory environment in Drosophila subobscura,2000,1990-1992,"Sintra, Portugal",lab,female,female,NA,NA,NA,NA,309,309,52,52,376,335,animal_model,half_sib,no,narrow,authors,both,adult,longevity,mean egg laying daily,survival,fertility,include,cor,-0.32,0.257142857,se,NA,NA,NA,NA,NA,NA,gen19,figure 2c,survival,fertility,family,-0.331647109,309,1,-0.331647109,female,cross,Insecta,between
1198,Drosophila subobscura,8,rayyan-178530585,Adaptation to the laboratory environment in Drosophila subobscura,2000,1990-1992,"Sintra, Portugal",lab,female,female,NA,NA,NA,NA,307,307,52,52,374,375,animal_model,half_sib,no,narrow,authors,adult,both,total egg laying in the third week of life,longevity,fertility,survival,include,cor,-0.148541114,0.424403183,se,NA,NA,NA,NA,NA,NA,gen29,figure 2a,fertility,survival,family,-0.149648302,307,1,-0.149648302,female,cross,Insecta,between
1199,Drosophila subobscura,8,rayyan-178530585,Adaptation to the laboratory environment in Drosophila subobscura,2000,1990-1992,"Sintra, Portugal",lab,female,female,NA,NA,NA,NA,168,168,56,56,235,374,animal_model,half_sib,no,narrow,authors,both,adult,longevity,thorax length,survival,size,include,cor,0.053092784,0.408247423,se,NA,NA,NA,NA,NA,NA,gen2,figure 2b,survival,size,family,0.053142755,168,1,0.053142755,female,cross,Insecta,between
1200,Drosophila subobscura,8,rayyan-178530585,Adaptation to the laboratory environment in Drosophila subobscura,2000,1990-1992,"Sintra, Portugal",lab,female,female,NA,NA,NA,NA,276,276,51,51,342,235,animal_model,half_sib,no,narrow,authors,both,adult,longevity,thorax length,survival,size,include,cor,-0.151030928,0.674742268,se,NA,NA,NA,NA,NA,NA,gen6,figure 2b,survival,size,family,-0.152195261,276,1,-0.152195261,female,cross,Insecta,between
1201,Drosophila subobscura,8,rayyan-178530585,Adaptation to the laboratory environment in Drosophila subobscura,2000,1990-1992,"Sintra, Portugal",lab,female,female,NA,NA,NA,NA,293,293,52,52,360,342,animal_model,half_sib,no,narrow,authors,both,adult,longevity,thorax length,survival,size,include,cor,-0.014948454,0.113402062,se,NA,NA,NA,NA,NA,NA,gen10,figure 2b,survival,size,family,-0.014949568,293,1,-0.014949568,female,cross,Insecta,between
1202,Drosophila subobscura,8,rayyan-178530585,Adaptation to the laboratory environment in Drosophila subobscura,2000,1990-1992,"Sintra, Portugal",lab,female,female,NA,NA,NA,NA,268,268,52,52,335,360,animal_model,half_sib,no,narrow,authors,both,adult,longevity,thorax length,survival,size,include,cor,0.036082474,0.243814433,se,NA,NA,NA,NA,NA,NA,gen15,figure 2b,survival,size,family,0.036098145,268,1,0.036098145,female,cross,Insecta,between
1203,Drosophila subobscura,8,rayyan-178530585,Adaptation to the laboratory environment in Drosophila subobscura,2000,1990-1992,"Sintra, Portugal",lab,female,female,NA,NA,NA,NA,309,309,52,52,376,335,animal_model,half_sib,no,narrow,authors,both,adult,longevity,thorax length,survival,size,include,cor,-0.162371134,0.368556701,se,NA,NA,NA,NA,NA,NA,gen19,figure 2b,survival,size,family,-0.163821079,309,1,-0.163821079,female,cross,Insecta,between
1204,Drosophila subobscura,8,rayyan-178530585,Adaptation to the laboratory environment in Drosophila subobscura,2000,1990-1992,"Sintra, Portugal",lab,female,female,NA,NA,NA,NA,308,308,52,52,375,376,animal_model,half_sib,no,narrow,authors,both,adult,longevity,thorax length,survival,size,include,cor,-0.547938144,0.510309278,se,NA,NA,NA,NA,NA,NA,gen25,figure 2b,survival,size,family,-0.615430037,308,1,-0.615430037,female,cross,Insecta,between
1205,Drosophila subobscura,8,rayyan-178530585,Adaptation to the laboratory environment in Drosophila subobscura,2000,1990-1992,"Sintra, Portugal",lab,female,female,NA,NA,NA,NA,307,307,52,52,374,375,animal_model,half_sib,no,narrow,authors,both,adult,longevity,thorax length,survival,size,include,cor,-0.037628866,0.521649485,se,NA,NA,NA,NA,NA,NA,gen29,figure 2b,survival,size,family,-0.037646641,307,1,-0.037646641,female,cross,Insecta,between
1206,Drosophila subobscura,8,rayyan-178530585,Adaptation to the laboratory environment in Drosophila subobscura,2000,1990-1992,"Sintra, Portugal",lab,female,female,NA,NA,NA,NA,168,168,56,56,235,374,animal_model,half_sib,no,narrow,authors,adult,adult,total egg laying,thorax length,fertility,size,include,cor,0.291237113,0.459278351,se,NA,NA,NA,NA,NA,NA,gen2,figure 2b,fertility,size,family,0.299917501,168,1,0.299917501,female,adult,Insecta,between
1207,Drosophila subobscura,8,rayyan-178530585,Adaptation to the laboratory environment in Drosophila subobscura,2000,1990-1992,"Sintra, Portugal",lab,female,female,NA,NA,NA,NA,276,276,51,51,342,235,animal_model,half_sib,no,narrow,authors,adult,adult,total egg laying,thorax length,fertility,size,include,cor,-0.151030928,0.413917526,se,NA,NA,NA,NA,NA,NA,gen6,figure 2b,fertility,size,family,-0.152195261,276,1,-0.152195261,female,adult,Insecta,between
1208,Drosophila subobscura,8,rayyan-178530585,Adaptation to the laboratory environment in Drosophila subobscura,2000,1990-1992,"Sintra, Portugal",lab,female,female,NA,NA,NA,NA,309,309,52,52,376,335,animal_model,half_sib,no,narrow,authors,both,adult,longevity,total egg laying,survival,fertility,include,cor,0.569633508,0.061256545,se,NA,NA,NA,NA,NA,NA,gen19,figure 2d,survival,fertility,family,0.646980142,309,1,0.646980142,female,cross,Insecta,between
1209,Drosophila subobscura,8,rayyan-178530585,Adaptation to the laboratory environment in Drosophila subobscura,2000,1990-1992,"Sintra, Portugal",lab,female,female,NA,NA,NA,NA,309,309,52,52,376,335,animal_model,half_sib,no,narrow,authors,adult,both,total egg laying in the third week of life,longevity,fertility,survival,include,cor,0.224933687,0.280106101,se,NA,NA,NA,NA,NA,NA,gen19,figure 2a,fertility,survival,family,0.228846699,309,1,0.228846699,female,cross,Insecta,between
1210,Drosophila subobscura,8,rayyan-178530585,Adaptation to the laboratory environment in Drosophila subobscura,2000,1990-1992,"Sintra, Portugal",lab,female,female,NA,NA,NA,NA,308,308,52,52,375,376,animal_model,half_sib,no,narrow,authors,adult,both,total egg laying in the third week of life,longevity,fertility,survival,include,cor,-0.174005305,0.458355438,se,NA,NA,NA,NA,NA,NA,gen25,figure 2a,fertility,survival,family,-0.175794084,308,1,-0.175794084,female,cross,Insecta,between
1211,Drosophila subobscura,8,rayyan-178530585,Adaptation to the laboratory environment in Drosophila subobscura,2000,1990-1992,"Sintra, Portugal",lab,female,female,NA,NA,NA,NA,308,308,52,52,375,376,animal_model,half_sib,no,narrow,authors,adult,adult,total egg laying,thorax length,fertility,size,include,cor,0.217525773,0.425257732,se,NA,NA,NA,NA,NA,NA,gen25,figure 2b,fertility,size,family,0.221057519,308,1,0.221057519,female,adult,Insecta,between
1212,Drosophila subobscura,8,rayyan-178530585,Adaptation to the laboratory environment in Drosophila subobscura,2000,1990-1992,"Sintra, Portugal",lab,female,female,NA,NA,NA,NA,307,307,52,52,374,375,animal_model,half_sib,no,narrow,authors,adult,adult,total egg laying,thorax length,fertility,size,include,cor,0.308247423,0.294845361,se,NA,NA,NA,NA,NA,NA,gen29,figure 2b,fertility,size,family,0.318607666,307,1,0.318607666,female,adult,Insecta,between
1213,Drosophila subobscura,8,rayyan-178530585,Adaptation to the laboratory environment in Drosophila subobscura,2000,1990-1992,"Sintra, Portugal",lab,female,female,NA,NA,NA,NA,293,293,52,52,352,342,animal_model,half_sib,no,narrow,authors,adult,adult,total egg laying in the sixth week of life,total egg laying,fertility,fertility,include,cor,0.583246073,0.306282723,se,NA,NA,NA,NA,NA,NA,gen10,figure 2d,fertility,fertility,family,0.667368275,293,1,0.667368275,female,adult,Insecta,within
1214,Drosophila subobscura,8,rayyan-178530585,Adaptation to the laboratory environment in Drosophila subobscura,2000,1990-1992,"Sintra, Portugal",lab,female,female,NA,NA,NA,NA,168,168,56,56,235,235,animal_model,half_sib,no,narrow,authors,adult,adult,total egg laying in the first week of life,total egg laying in the sixth week of life,fertility,fertility,include,cor,0.674801061,0.381962865,se,NA,NA,NA,NA,NA,NA,gen2,figure 2a,fertility,fertility,family,0.819506276,168,1,0.819506276,female,adult,Insecta,within
1215,Drosophila subobscura,8,rayyan-178530585,Adaptation to the laboratory environment in Drosophila subobscura,2000,1990-1992,"Sintra, Portugal",lab,female,female,NA,NA,NA,NA,307,307,52,52,374,375,animal_model,half_sib,no,narrow,authors,both,non_adult,longevity,time of development (emergence),survival,reverse_maturation,include,cor,-0.34,0.413333333,se,NA,NA,NA,NA,NA,NA,gen29,figure 2e,survival,maturation,family,-0.354092529,307,-1,0.354092529,female,cross,Insecta,between
1216,Drosophila subobscura,8,rayyan-178530585,Adaptation to the laboratory environment in Drosophila subobscura,2000,1990-1992,"Sintra, Portugal",lab,female,female,NA,NA,NA,NA,293,293,52,52,360,352,animal_model,half_sib,no,narrow,authors,adult,adult,total egg laying in the first week of life,total egg laying in the sixth week of life,fertility,fertility,include,cor,-0.267374005,0.322546419,se,NA,NA,NA,NA,NA,NA,gn10,figure 2a,fertility,fertility,family,-0.274033497,293,1,-0.274033497,female,adult,Insecta,within
1217,Drosophila subobscura,8,rayyan-178530585,Adaptation to the laboratory environment in Drosophila subobscura,2000,1990-1992,"Sintra, Portugal",lab,female,female,NA,NA,NA,NA,268,268,52,52,335,301,animal_model,half_sib,no,narrow,authors,adult,adult,total egg laying in the first week of life,total egg laying in the sixth week of life,fertility,fertility,include,cor,-0.827586207,0.203713528,se,NA,NA,NA,NA,NA,NA,gen15,figure 2a,fertility,fertility,family,-1.180427001,268,1,-1.180427001,female,adult,Insecta,within
1218,Drosophila subobscura,8,rayyan-178530585,Adaptation to the laboratory environment in Drosophila subobscura,2000,1990-1992,"Sintra, Portugal",lab,female,female,NA,NA,NA,NA,309,309,52,52,376,370,animal_model,half_sib,no,narrow,authors,adult,adult,total egg laying in the first week of life,total egg laying in the sixth week of life,fertility,fertility,include,cor,0.462599469,0.212201592,se,NA,NA,NA,NA,NA,NA,gen19,figure 2a,fertility,fertility,family,0.500613453,309,1,0.500613453,female,adult,Insecta,within
1219,Drosophila subobscura,8,rayyan-178530585,Adaptation to the laboratory environment in Drosophila subobscura,2000,1990-1992,"Sintra, Portugal",lab,female,female,NA,NA,NA,NA,308,308,52,52,375,376,animal_model,half_sib,no,narrow,authors,adult,non_adult,thorax length,time of development (emergence),size,reverse_maturation,include,cor,-0.088659794,0.260824742,se,NA,NA,NA,NA,NA,NA,gen25,figure 2b,size,maturation,family,-0.088893201,308,-1,0.088893201,female,cross,Insecta,between
1220,Drosophila subobscura,8,rayyan-178530585,Adaptation to the laboratory environment in Drosophila subobscura,2000,1990-1992,"Sintra, Portugal",lab,female,female,NA,NA,NA,NA,307,307,52,52,374,375,animal_model,half_sib,no,narrow,authors,adult,non_adult,thorax length,time of development (emergence),size,reverse_maturation,include,cor,0.194845361,0.283505155,se,NA,NA,NA,NA,NA,NA,gen29,figure 2b,size,maturation,family,0.197368847,307,-1,-0.197368847,female,cross,Insecta,between
1221,Drosophila subobscura,8,rayyan-178530585,Adaptation to the laboratory environment in Drosophila subobscura,2000,1990-1992,"Sintra, Portugal",lab,female,female,NA,NA,NA,NA,168,168,56,56,235,235,animal_model,half_sib,no,narrow,authors,adult,both,total egg laying in the first week of life,longevity,fertility,survival,include,cor,-0.021220159,0.314058355,se,NA,NA,NA,NA,NA,NA,gen2,figure 2a,fertility,survival,family,-0.021223345,168,1,-0.021223345,female,cross,Insecta,between
1222,Drosophila subobscura,8,rayyan-178530585,Adaptation to the laboratory environment in Drosophila subobscura,2000,1990-1992,"Sintra, Portugal",lab,female,female,NA,NA,NA,NA,276,276,51,51,342,342,animal_model,half_sib,no,narrow,authors,adult,both,total egg laying in the first week of life,longevity,fertility,survival,include,cor,0.199469496,0.466843501,se,NA,NA,NA,NA,NA,NA,gen6,figure 2a,fertility,survival,family,0.202180007,276,1,0.202180007,female,cross,Insecta,between
1223,Drosophila subobscura,8,rayyan-178530585,Adaptation to the laboratory environment in Drosophila subobscura,2000,1990-1992,"Sintra, Portugal",lab,female,female,NA,NA,NA,NA,293,293,52,52,360,360,animal_model,half_sib,no,narrow,authors,adult,both,total egg laying in the first week of life,longevity,fertility,survival,include,cor,-0.157029178,0.50928382,se,NA,NA,NA,NA,NA,NA,gen10,figure 2a,fertility,survival,family,-0.1583393,293,1,-0.1583393,female,cross,Insecta,between
1224,Drosophila subobscura,8,rayyan-178530585,Adaptation to the laboratory environment in Drosophila subobscura,2000,1990-1992,"Sintra, Portugal",lab,female,female,NA,NA,NA,NA,268,268,52,52,335,335,animal_model,half_sib,no,narrow,authors,adult,both,total egg laying in the first week of life,longevity,fertility,survival,include,cor,-0.343766578,0.271618037,se,NA,NA,NA,NA,NA,NA,gen15,figure 2a,fertility,survival,family,-0.358357639,268,1,-0.358357639,female,cross,Insecta,between
1225,Drosophila subobscura,8,rayyan-178530585,Adaptation to the laboratory environment in Drosophila subobscura,2000,1990-1992,"Sintra, Portugal",lab,female,female,NA,NA,NA,NA,309,309,52,52,376,376,animal_model,half_sib,no,narrow,authors,adult,both,total egg laying in the first week of life,longevity,fertility,survival,include,cor,0.021220159,0.288594164,se,NA,NA,NA,NA,NA,NA,gen19,figure 2a,fertility,survival,family,0.021223345,309,1,0.021223345,female,cross,Insecta,between
1226,Drosophila subobscura,8,rayyan-178530585,Adaptation to the laboratory environment in Drosophila subobscura,2000,1990-1992,"Sintra, Portugal",lab,female,female,NA,NA,NA,NA,308,308,52,52,375,375,animal_model,half_sib,no,narrow,authors,adult,both,total egg laying in the first week of life,longevity,fertility,survival,include,cor,-0.386206897,0.297082228,se,NA,NA,NA,NA,NA,NA,gen25,figure 2a,fertility,survival,family,-0.40733427,308,1,-0.40733427,female,cross,Insecta,between
1227,Drosophila subobscura,8,rayyan-178530585,Adaptation to the laboratory environment in Drosophila subobscura,2000,1990-1992,"Sintra, Portugal",lab,female,female,NA,NA,NA,NA,307,307,52,52,374,374,animal_model,half_sib,no,narrow,authors,adult,both,total egg laying in the first week of life,longevity,fertility,survival,include,cor,-0.055172414,0.424403183,se,NA,NA,NA,NA,NA,NA,gen29,figure 2a,fertility,survival,family,-0.055228498,307,1,-0.055228498,female,cross,Insecta,between
1228,Drosophila subobscura,8,rayyan-178530585,Adaptation to the laboratory environment in Drosophila subobscura,2000,1990-1992,"Sintra, Portugal",lab,female,female,NA,NA,NA,NA,276,276,51,51,342,322,animal_model,half_sib,no,narrow,authors,adult,adult,total egg laying in the third week of life,total egg laying in the sixth week of life,fertility,fertility,include,cor,0.589920424,0.398938992,se,NA,NA,NA,NA,NA,NA,gen6,figure 2a,fertility,fertility,family,0.677544009,276,1,0.677544009,female,adult,Insecta,within
1229,Drosophila subobscura,8,rayyan-178530585,Adaptation to the laboratory environment in Drosophila subobscura,2000,1990-1992,"Sintra, Portugal",lab,female,female,NA,NA,NA,NA,293,293,52,52,360,352,animal_model,half_sib,no,narrow,authors,adult,adult,total egg laying in the third week of life,total egg laying in the sixth week of life,fertility,fertility,include,cor,NA,0.492307692,se,NA,NA,NA,NA,NA,NA,gen10,figure 2a,fertility,fertility,family,NA,293,1,NA,female,adult,Insecta,within
1230,Drosophila subobscura,8,rayyan-178530585,Adaptation to the laboratory environment in Drosophila subobscura,2000,1990-1992,"Sintra, Portugal",lab,female,female,NA,NA,NA,NA,268,268,52,52,335,301,animal_model,half_sib,no,narrow,authors,adult,adult,total egg laying in the third week of life,total egg laying in the sixth week of life,fertility,fertility,include,cor,NA,0.0933687,se,NA,NA,NA,NA,NA,NA,gen15,figure 2a,fertility,fertility,family,NA,268,1,NA,female,adult,Insecta,within
1231,Drosophila subobscura,8,rayyan-178530585,Adaptation to the laboratory environment in Drosophila subobscura,2000,1990-1992,"Sintra, Portugal",lab,female,female,NA,NA,NA,NA,268,268,52,52,301,360,animal_model,half_sib,no,narrow,authors,adult,non_adult,total egg laying in the sixth week of life,time of development (emergence),fertility,reverse_maturation,include,cor,0.226666667,0.3,se,NA,NA,NA,NA,NA,NA,gen15,figure 2e,fertility,maturation,family,0.230672784,268,-1,-0.230672784,female,cross,Insecta,between
1232,Drosophila subobscura,8,rayyan-178530585,Adaptation to the laboratory environment in Drosophila subobscura,2000,1990-1992,"Sintra, Portugal",lab,female,female,NA,NA,NA,NA,309,309,52,52,370,335,animal_model,half_sib,no,narrow,authors,adult,non_adult,total egg laying in the sixth week of life,time of development (emergence),fertility,reverse_maturation,include,cor,-0.44,0.42,se,NA,NA,NA,NA,NA,NA,gen19,figure 2e,fertility,maturation,family,-0.472230804,309,-1,0.472230804,female,cross,Insecta,between
1233,Drosophila subobscura,8,rayyan-178530585,Adaptation to the laboratory environment in Drosophila subobscura,2000,1990-1992,"Sintra, Portugal",lab,female,female,NA,NA,NA,NA,308,308,52,52,344,376,animal_model,half_sib,no,narrow,authors,adult,non_adult,total egg laying in the sixth week of life,time of development (emergence),fertility,reverse_maturation,include,cor,-0.62,0.253333333,se,NA,NA,NA,NA,NA,NA,gen25,figure 2e,fertility,maturation,family,-0.725005088,308,-1,0.725005088,female,cross,Insecta,between
1234,Drosophila subobscura,8,rayyan-178530585,Adaptation to the laboratory environment in Drosophila subobscura,2000,1990-1992,"Sintra, Portugal",lab,female,female,NA,NA,NA,NA,307,307,52,52,302,375,animal_model,half_sib,no,narrow,authors,adult,non_adult,total egg laying in the sixth week of life,time of development (emergence),fertility,reverse_maturation,include,cor,-0.146666667,0.466666667,se,NA,NA,NA,NA,NA,NA,gen29,figure 2e,fertility,maturation,family,-0.147732107,307,-1,0.147732107,female,cross,Insecta,between
1235,Drosophila subobscura,8,rayyan-178530585,Adaptation to the laboratory environment in Drosophila subobscura,2000,1990-1992,"Sintra, Portugal",lab,female,female,NA,NA,NA,NA,168,168,56,56,235,374,animal_model,half_sib,no,narrow,authors,both,non_adult,longevity,time of development (emergence),survival,reverse_maturation,include,cor,0.493333333,0.2,se,NA,NA,NA,NA,NA,NA,gen2,figure 2e,survival,maturation,family,0.540456355,168,-1,-0.540456355,female,cross,Insecta,between
1236,Drosophila subobscura,8,rayyan-178530585,Adaptation to the laboratory environment in Drosophila subobscura,2000,1990-1992,"Sintra, Portugal",lab,female,female,NA,NA,NA,NA,268,268,52,52,335,360,animal_model,half_sib,no,narrow,authors,adult,non_adult,total egg laying in the third week of life,time of development (emergence),fertility,reverse_maturation,include,cor,-0.473333333,0.4,se,NA,NA,NA,NA,NA,NA,gen15,figure 2e,fertility,maturation,family,-0.514357424,268,-1,0.514357424,female,cross,Insecta,between
1237,Drosophila subobscura,8,rayyan-178530585,Adaptation to the laboratory environment in Drosophila subobscura,2000,1990-1992,"Sintra, Portugal",lab,female,female,NA,NA,NA,NA,307,307,52,52,374,375,animal_model,half_sib,no,narrow,authors,both,adult,longevity,total egg laying,survival,fertility,include,cor,0.052356021,0.401570681,se,NA,NA,NA,NA,NA,NA,gen29,figure 2d,survival,fertility,family,0.052403938,307,1,0.052403938,female,cross,Insecta,between
1238,Drosophila subobscura,8,rayyan-178530585,Adaptation to the laboratory environment in Drosophila subobscura,2000,1990-1992,"Sintra, Portugal",lab,female,female,NA,NA,NA,NA,309,309,52,52,376,335,animal_model,half_sib,no,narrow,authors,adult,non_adult,total egg laying in the third week of life,time of development (emergence),fertility,reverse_maturation,include,cor,0.286666667,0.306666667,se,NA,NA,NA,NA,NA,NA,gen19,figure 2e,fertility,maturation,family,0.294930678,309,-1,-0.294930678,female,cross,Insecta,between
1239,Drosophila subobscura,8,rayyan-178530585,Adaptation to the laboratory environment in Drosophila subobscura,2000,1990-1992,"Sintra, Portugal",lab,female,female,NA,NA,NA,NA,308,308,52,52,375,376,animal_model,half_sib,no,narrow,authors,adult,non_adult,total egg laying in the third week of life,time of development (emergence),fertility,reverse_maturation,include,cor,-0.1,0.266666667,se,NA,NA,NA,NA,NA,NA,gen25,figure 2e,fertility,maturation,family,-0.100335348,308,-1,0.100335348,female,cross,Insecta,between
1240,Drosophila subobscura,8,rayyan-178530585,Adaptation to the laboratory environment in Drosophila subobscura,2000,1990-1992,"Sintra, Portugal",lab,female,female,NA,NA,NA,NA,307,307,52,52,374,375,animal_model,half_sib,no,narrow,authors,adult,non_adult,total egg laying in the third week of life,time of development (emergence),fertility,reverse_maturation,include,cor,0.326666667,0.133333333,se,NA,NA,NA,NA,NA,NA,gen29,figure 2e,fertility,maturation,family,0.339092154,307,-1,-0.339092154,female,cross,Insecta,between
1241,Drosophila subobscura,8,rayyan-178530585,Adaptation to the laboratory environment in Drosophila subobscura,2000,1990-1992,"Sintra, Portugal",lab,female,female,NA,NA,NA,NA,168,168,56,56,235,374,animal_model,half_sib,no,narrow,authors,adult,non_adult,total egg laying in the sixth week of life,time of development (emergence),fertility,reverse_maturation,include,cor,0.193333333,0.353333333,se,NA,NA,NA,NA,NA,NA,gen2,figure 2e,fertility,maturation,family,0.19579763,168,-1,-0.19579763,female,cross,Insecta,between
1242,Drosophila subobscura,8,rayyan-178530585,Adaptation to the laboratory environment in Drosophila subobscura,2000,1990-1992,"Sintra, Portugal",lab,female,female,NA,NA,NA,NA,276,276,51,51,322,235,animal_model,half_sib,no,narrow,authors,adult,non_adult,total egg laying in the sixth week of life,time of development (emergence),fertility,reverse_maturation,include,cor,-0.286666667,0.153333333,se,NA,NA,NA,NA,NA,NA,gen6,figure 2e,fertility,maturation,family,-0.294930678,276,-1,0.294930678,female,cross,Insecta,between
1243,Drosophila subobscura,8,rayyan-178530585,Adaptation to the laboratory environment in Drosophila subobscura,2000,1990-1992,"Sintra, Portugal",lab,female,female,NA,NA,NA,NA,293,293,52,52,352,342,animal_model,half_sib,no,narrow,authors,adult,non_adult,total egg laying in the sixth week of life,time of development (emergence),fertility,reverse_maturation,include,cor,-0.273333333,0.426666667,se,NA,NA,NA,NA,NA,NA,gen10,figure 2e,fertility,maturation,family,-0.280462773,293,-1,0.280462773,female,cross,Insecta,between
1244,Drosophila subobscura,8,rayyan-178530585,Adaptation to the laboratory environment in Drosophila subobscura,2000,1990-1992,"Sintra, Portugal",lab,female,female,NA,NA,NA,NA,307,307,52,52,374,302,animal_model,half_sib,no,narrow,authors,adult,adult,total egg laying in the first week of life,total egg laying in the sixth week of life,fertility,fertility,include,cor,0.751193634,0.373474801,se,NA,NA,NA,NA,NA,NA,gen29,figure 2a,fertility,fertility,family,0.975688982,307,1,0.975688982,female,adult,Insecta,within
1245,Drosophila subobscura,8,rayyan-178530585,Adaptation to the laboratory environment in Drosophila subobscura,2000,1990-1992,"Sintra, Portugal",lab,female,female,NA,NA,NA,NA,308,308,52,52,375,376,animal_model,half_sib,no,narrow,authors,both,adult,longevity,total egg laying,survival,fertility,include,cor,0.767015707,0.061256545,se,NA,NA,NA,NA,NA,NA,gen25,figure 2d,survival,fertility,family,1.013038161,308,1,1.013038161,female,cross,Insecta,between
1246,Drosophila subobscura,8,rayyan-178530585,Adaptation to the laboratory environment in Drosophila subobscura,2000,1990-1992,"Sintra, Portugal",lab,female,female,NA,NA,NA,NA,309,309,52,52,376,335,animal_model,half_sib,no,narrow,authors,adult,non_adult,thorax length,time of development (emergence),size,reverse_maturation,include,cor,0.251546392,0.345876289,se,NA,NA,NA,NA,NA,NA,gen19,figure 2b,size,maturation,family,0.257062979,309,-1,-0.257062979,female,cross,Insecta,between
1247,Drosophila subobscura,8,rayyan-178530585,Adaptation to the laboratory environment in Drosophila subobscura,2000,1990-1992,"Sintra, Portugal",lab,female,female,NA,NA,NA,NA,308,308,52,52,375,344,animal_model,half_sib,no,narrow,authors,adult,adult,total egg laying in the first week of life,total egg laying in the sixth week of life,fertility,fertility,include,cor,-0.369230769,0.331034483,se,NA,NA,NA,NA,NA,NA,gen25,figure 2a,fertility,fertility,family,-0.387532151,308,1,-0.387532151,female,adult,Insecta,within
1248,Drosophila subobscura,8,rayyan-178530585,Adaptation to the laboratory environment in Drosophila subobscura,2000,1990-1992,"Sintra, Portugal",lab,female,female,NA,NA,NA,NA,268,268,52,52,335,360,animal_model,half_sib,no,narrow,authors,both,non_adult,longevity,time of development (emergence),survival,reverse_maturation,include,cor,0.506666667,0.333333333,se,NA,NA,NA,NA,NA,NA,gen15,figure 2e,survival,maturation,family,0.558234953,268,-1,-0.558234953,female,cross,Insecta,between
1249,Drosophila subobscura,8,rayyan-178530585,Adaptation to the laboratory environment in Drosophila subobscura,2000,1990-1992,"Sintra, Portugal",lab,female,female,NA,NA,NA,NA,309,309,52,52,376,335,animal_model,half_sib,no,narrow,authors,both,non_adult,longevity,time of development (emergence),survival,reverse_maturation,include,cor,-0.5,0.433333333,se,NA,NA,NA,NA,NA,NA,gen19,figure 2e,survival,maturation,family,-0.549306144,309,-1,0.549306144,female,cross,Insecta,between
1250,Drosophila subobscura,8,rayyan-178530585,Adaptation to the laboratory environment in Drosophila subobscura,2000,1990-1992,"Sintra, Portugal",lab,female,female,NA,NA,NA,NA,293,293,52,52,360,342,animal_model,half_sib,no,narrow,authors,adult,adult,total egg laying,thorax length,fertility,size,include,cor,0.13814433,0.487628866,se,NA,NA,NA,NA,NA,NA,gen10,figure 2b,fertility,size,family,0.139033307,293,1,0.139033307,female,adult,Insecta,between
1251,Drosophila subobscura,8,rayyan-178530585,Adaptation to the laboratory environment in Drosophila subobscura,2000,1990-1992,"Sintra, Portugal",lab,female,female,NA,NA,NA,NA,309,309,52,52,376,335,animal_model,half_sib,no,narrow,authors,adult,adult,total egg laying,thorax length,fertility,size,include,cor,0.041752577,0.328865979,se,NA,NA,NA,NA,NA,NA,gen19,figure 2b,fertility,size,family,0.041776865,309,1,0.041776865,female,adult,Insecta,between
1252,Drosophila subobscura,8,rayyan-178530585,Adaptation to the laboratory environment in Drosophila subobscura,2000,1990-1992,"Sintra, Portugal",lab,female,female,NA,NA,NA,NA,268,268,52,52,335,360,animal_model,half_sib,no,narrow,authors,adult,adult,total egg laying,thorax length,fertility,size,include,cor,-0.037628866,0.232474227,se,NA,NA,NA,NA,NA,NA,gen15,figure 2b,fertility,size,family,-0.037646641,268,1,-0.037646641,female,adult,Insecta,between
1253,Drosophila subobscura,8,rayyan-178530585,Adaptation to the laboratory environment in Drosophila subobscura,2000,1990-1992,"Sintra, Portugal",lab,female,female,NA,NA,NA,NA,293,293,52,52,360,342,animal_model,half_sib,no,narrow,authors,both,non_adult,longevity,time of development (emergence),survival,reverse_maturation,include,cor,0.626666667,0.44,se,NA,NA,NA,NA,NA,NA,gen10,figure 2e,survival,maturation,family,0.735908268,293,-1,-0.735908268,female,cross,Insecta,between
1254,Drosophila subobscura,8,rayyan-178530585,Adaptation to the laboratory environment in Drosophila subobscura,2000,1990-1992,"Sintra, Portugal",lab,female,female,NA,NA,NA,NA,168,168,56,56,235,374,animal_model,half_sib,no,narrow,authors,adult,non_adult,thorax length,time of development (emergence),size,reverse_maturation,include,cor,0.087113402,0.334536082,se,NA,NA,NA,NA,NA,NA,gen2,figure 2b,size,maturation,family,0.087334771,168,-1,-0.087334771,female,cross,Insecta,between
1255,Drosophila subobscura,8,rayyan-178530585,Adaptation to the laboratory environment in Drosophila subobscura,2000,1990-1992,"Sintra, Portugal",lab,female,female,NA,NA,NA,NA,308,308,52,52,375,376,animal_model,half_sib,no,narrow,authors,both,non_adult,longevity,time of development (emergence),survival,reverse_maturation,include,cor,-0.4,0.173333333,se,NA,NA,NA,NA,NA,NA,gen25,figure 2e,survival,maturation,family,-0.42364893,308,-1,0.42364893,female,cross,Insecta,between
1256,Drosophila subobscura,8,rayyan-178530585,Adaptation to the laboratory environment in Drosophila subobscura,2000,1990-1992,"Sintra, Portugal",lab,female,female,NA,NA,NA,NA,276,276,51,51,342,235,animal_model,half_sib,no,narrow,authors,both,non_adult,longevity,time of development (emergence),survival,reverse_maturation,include,cor,-0.14,0.16,se,NA,NA,NA,NA,NA,NA,gen6,figure 2e,survival,maturation,family,-0.140925576,276,-1,0.140925576,female,cross,Insecta,between
1257,Epiphyas postvittana,246,rayyan-197247412,Genetic variation in the life-history traits of Epiphyas postvittana: Population structure and local adaptation,2000,NA,"Melbourne, Australia",lab,both,female,81,81,NA,NA,81,81,27,27,291,291,animal_model,half_sib,no,narrow,authors,adult,non_adult,body weight on the day of emergence,age at first reproduction (the interval between adult emergence and the first day of egg-laying),size,reverse_maturation,include,cor,-0.292,0.233,se,NA,NA,NA,NA,NA,NA,Melbourne_23,table 2,size,maturation,family,-0.300751295,81,-1,0.300751295,female,cross,Insecta,between
1258,Epiphyas postvittana,246,rayyan-197247412,Genetic variation in the life-history traits of Epiphyas postvittana: Population structure and local adaptation,2000,NA,"Melbourne, Australia",lab,both,both,81,81,NA,NA,81,81,27,27,291,291,animal_model,half_sib,no,narrow,authors,non_adult,adult,development time,total fecundity,reverse_maturation,fertility,include,cor,-0.226,0.138,se,NA,NA,NA,NA,NA,NA,Melbourne_23,table 2,maturation,fertility,family,-0.229970121,81,-1,0.229970121,both,cross,Insecta,between
1259,Epiphyas postvittana,246,rayyan-197247412,Genetic variation in the life-history traits of Epiphyas postvittana: Population structure and local adaptation,2000,NA,"Melbourne, Australia",lab,both,female,81,81,NA,NA,81,81,27,27,291,291,animal_model,half_sib,no,narrow,authors,adult,both,body weight on the day of emergence,adult lifespan,size,survival,include,cor,0.208,0.162,se,NA,NA,NA,NA,NA,NA,Melbourne_23,table 2,size,survival,family,0.211079993,81,1,0.211079993,female,cross,Insecta,between
1260,Epiphyas postvittana,246,rayyan-197247412,Genetic variation in the life-history traits of Epiphyas postvittana: Population structure and local adaptation,2000,NA,"Melbourne, Australia",lab,both,female,81,81,NA,NA,81,81,27,27,291,291,animal_model,half_sib,no,narrow,authors,non_adult,adult,development time,number of eggs laid during the first 5 days (early),reverse_maturation,fertility,include,cor,-0.205,0.167,se,NA,NA,NA,NA,NA,NA,Melbourne_23,table 2,maturation,fertility,family,-0.207946366,81,-1,0.207946366,female,cross,Insecta,between
1261,Epiphyas postvittana,246,rayyan-197247412,Genetic variation in the life-history traits of Epiphyas postvittana: Population structure and local adaptation,2000,NA,"Melbourne, Australia",lab,both,female,81,81,NA,NA,81,81,27,27,291,291,animal_model,half_sib,no,narrow,authors,adult,adult,body weight on the day of emergence,number of eggs laid during the first 5 days (early),size,fertility,include,cor,-0.049,0.241,se,NA,NA,NA,NA,NA,NA,Melbourne_23,table 2,size,fertility,family,-0.049039273,81,1,-0.049039273,female,adult,Insecta,between
1262,Epiphyas postvittana,246,rayyan-197247412,Genetic variation in the life-history traits of Epiphyas postvittana: Population structure and local adaptation,2000,NA,"Melbourne, Australia",lab,both,female,81,81,NA,NA,81,81,27,27,291,291,animal_model,half_sib,no,narrow,authors,adult,adult,body weight on the day of emergence,total fecundity,size,fertility,include,cor,0.151,0.261,se,NA,NA,NA,NA,NA,NA,Melbourne_23,table 2,size,fertility,family,0.152163611,81,1,0.152163611,female,adult,Insecta,between
1263,Epiphyas postvittana,246,rayyan-197247412,Genetic variation in the life-history traits of Epiphyas postvittana: Population structure and local adaptation,2000,NA,"Canberra, Australia",lab,both,female,96,96,NA,NA,96,96,32,32,339,339,animal_model,half_sib,no,narrow,authors,adult,adult,body weight on the day of emergence,total fecundity,size,fertility,include,cor,-0.031,0.277,se,NA,NA,NA,NA,NA,NA,Canberra_23,table 2,size,fertility,family,-0.031009936,96,1,-0.031009936,female,adult,Insecta,between
1264,Epiphyas postvittana,246,rayyan-197247412,Genetic variation in the life-history traits of Epiphyas postvittana: Population structure and local adaptation,2000,NA,"Canberra, Australia",lab,both,both,96,96,NA,NA,96,96,32,32,339,339,animal_model,half_sib,no,narrow,authors,non_adult,both,development time,adult lifespan,reverse_maturation,survival,include,cor,0.62,0.227,se,NA,NA,NA,NA,NA,NA,Canberra_23,table 2,maturation,survival,family,0.725005088,96,-1,-0.725005088,both,cross,Insecta,between
1265,Epiphyas postvittana,246,rayyan-197247412,Genetic variation in the life-history traits of Epiphyas postvittana: Population structure and local adaptation,2000,NA,"Canberra, Australia",lab,both,female,96,96,NA,NA,96,96,32,32,335,335,animal_model,half_sib,no,narrow,authors,non_adult,non_adult,development time,age at first reproduction (the interval between adult emergence and the first day of egg-laying),reverse_maturation,reverse_maturation,include,cor,0.346,0.25,se,NA,NA,NA,NA,NA,NA,Canberra_28,table 3,maturation,maturation,family,0.360892579,96,1,0.360892579,female,non_adult,Insecta,within
1266,Epiphyas postvittana,246,rayyan-197247412,Genetic variation in the life-history traits of Epiphyas postvittana: Population structure and local adaptation,2000,NA,"Melbourne, Australia",lab,both,female,81,81,NA,NA,81,81,27,27,291,291,animal_model,half_sib,no,narrow,authors,both,adult,adult lifespan,total fecundity,survival,fertility,include,cor,-0.032,0.177,se,NA,NA,NA,NA,NA,NA,Melbourne_23,table 2,survival,fertility,family,-0.032010929,81,1,-0.032010929,female,cross,Insecta,between
1267,Epiphyas postvittana,246,rayyan-197247412,Genetic variation in the life-history traits of Epiphyas postvittana: Population structure and local adaptation,2000,NA,"Canberra, Australia",lab,both,both,96,96,NA,NA,96,96,32,32,335,335,animal_model,half_sib,no,narrow,authors,non_adult,adult,development time,body weight on the day of emergence,reverse_maturation,size,include,cor,0.539,0.186,se,NA,NA,NA,NA,NA,NA,Canberra_28,table 3,maturation,size,family,0.602745045,96,-1,-0.602745045,both,cross,Insecta,between
1268,Epiphyas postvittana,246,rayyan-197247412,Genetic variation in the life-history traits of Epiphyas postvittana: Population structure and local adaptation,2000,NA,"Canberra, Australia",lab,both,female,96,96,NA,NA,96,96,32,32,339,339,animal_model,half_sib,no,narrow,authors,adult,adult,body weight on the day of emergence,number of eggs laid during the first 5 days (early),size,fertility,include,cor,0.288,0.214,se,NA,NA,NA,NA,NA,NA,Canberra_23,table 2,size,fertility,family,0.296383998,96,1,0.296383998,female,adult,Insecta,between
1269,Epiphyas postvittana,246,rayyan-197247412,Genetic variation in the life-history traits of Epiphyas postvittana: Population structure and local adaptation,2000,NA,"Canberra, Australia",lab,both,female,96,96,NA,NA,96,96,32,32,339,339,animal_model,half_sib,no,narrow,authors,both,non_adult,adult lifespan,age at first reproduction (the interval between adult emergence and the first day of egg-laying),survival,reverse_maturation,include,cor,0.815,0.24,se,NA,NA,NA,NA,NA,NA,Canberra_23,table 2,survival,maturation,family,1.141742461,96,-1,-1.141742461,female,cross,Insecta,between
1270,Epiphyas postvittana,246,rayyan-197247412,Genetic variation in the life-history traits of Epiphyas postvittana: Population structure and local adaptation,2000,NA,"Melbourne, Australia",lab,female,female,81,81,NA,NA,81,81,27,27,289,289,animal_model,half_sib,no,narrow,authors,non_adult,adult,age at first reproduction (the interval between adult emergence and the first day of egg-laying),total fecundity,reverse_maturation,fertility,include,cor,-0.572,0.321,se,NA,NA,NA,NA,NA,NA,Melbourne_28,table 3,maturation,fertility,family,-0.650490389,81,-1,0.650490389,female,cross,Insecta,between
1271,Epiphyas postvittana,246,rayyan-197247412,Genetic variation in the life-history traits of Epiphyas postvittana: Population structure and local adaptation,2000,NA,"Melbourne, Australia",lab,female,female,81,81,NA,NA,81,81,27,27,289,289,animal_model,half_sib,no,narrow,authors,adult,adult,number of eggs laid during the first 5 days (early),total fecundity,fertility,fertility,include,cor,0.773,0.204,se,NA,NA,NA,NA,NA,NA,Melbourne_28,table 3,fertility,fertility,family,1.027739144,81,1,1.027739144,female,adult,Insecta,within
1272,Epiphyas postvittana,246,rayyan-197247412,Genetic variation in the life-history traits of Epiphyas postvittana: Population structure and local adaptation,2000,NA,"Canberra, Australia",lab,female,female,96,96,NA,NA,96,96,32,32,339,339,animal_model,half_sib,no,narrow,authors,non_adult,adult,age at first reproduction (the interval between adult emergence and the first day of egg-laying),number of eggs laid during the first 5 days (early),reverse_maturation,fertility,include,cor,-0.372,0.304,se,NA,NA,NA,NA,NA,NA,Canberra_23,table 2,maturation,fertility,family,-0.390742321,96,-1,0.390742321,female,cross,Insecta,between
1273,Epiphyas postvittana,246,rayyan-197247412,Genetic variation in the life-history traits of Epiphyas postvittana: Population structure and local adaptation,2000,NA,"Melbourne, Australia",lab,female,female,81,81,NA,NA,81,81,27,27,291,291,animal_model,half_sib,no,narrow,authors,non_adult,adult,age at first reproduction (the interval between adult emergence and the first day of egg-laying),total fecundity,reverse_maturation,fertility,include,cor,-0.307,0.253,se,NA,NA,NA,NA,NA,NA,Melbourne_23,table 2,maturation,fertility,family,-0.317229857,81,-1,0.317229857,female,cross,Insecta,between
1274,Epiphyas postvittana,246,rayyan-197247412,Genetic variation in the life-history traits of Epiphyas postvittana: Population structure and local adaptation,2000,NA,"Canberra, Australia",lab,both,female,96,96,NA,NA,96,96,32,32,339,339,animal_model,half_sib,no,narrow,authors,both,adult,adult lifespan,number of eggs laid during the first 5 days (early),survival,fertility,include,cor,-0.334,0.167,se,NA,NA,NA,NA,NA,NA,Canberra_23,table 2,survival,fertility,family,-0.347323778,96,1,-0.347323778,female,cross,Insecta,between
1275,Epiphyas postvittana,246,rayyan-197247412,Genetic variation in the life-history traits of Epiphyas postvittana: Population structure and local adaptation,2000,NA,"Melbourne, Australia",lab,both,female,81,81,NA,NA,81,81,27,27,291,291,animal_model,half_sib,no,narrow,authors,both,adult,adult lifespan,number of eggs laid during the first 5 days (early),survival,fertility,include,cor,-0.332,0.155,se,NA,NA,NA,NA,NA,NA,Melbourne_23,table 2,survival,fertility,family,-0.345074339,81,1,-0.345074339,female,cross,Insecta,between
1276,Epiphyas postvittana,246,rayyan-197247412,Genetic variation in the life-history traits of Epiphyas postvittana: Population structure and local adaptation,2000,NA,"Melbourne, Australia",lab,both,female,81,81,NA,NA,81,81,27,27,289,289,animal_model,half_sib,no,narrow,authors,both,non_adult,adult lifespan,age at first reproduction (the interval between adult emergence and the first day of egg-laying),survival,reverse_maturation,include,cor,0.223,0.138,se,NA,NA,NA,NA,NA,NA,Melbourne_28,table 3,survival,maturation,family,0.226810893,81,-1,-0.226810893,female,cross,Insecta,between
1277,Epiphyas postvittana,246,rayyan-197247412,Genetic variation in the life-history traits of Epiphyas postvittana: Population structure and local adaptation,2000,NA,"Melbourne, Australia",lab,both,female,81,81,NA,NA,81,81,27,27,289,289,animal_model,half_sib,no,narrow,authors,adult,adult,body weight on the day of emergence,total fecundity,size,fertility,include,cor,NA,0.193,se,NA,NA,NA,NA,NA,NA,Melbourne_28,table 3,size,fertility,family,NA,81,1,NA,female,adult,Insecta,between
1278,Epiphyas postvittana,246,rayyan-197247412,Genetic variation in the life-history traits of Epiphyas postvittana: Population structure and local adaptation,2000,NA,"Melbourne, Australia",lab,female,female,81,81,NA,NA,81,81,27,27,289,289,animal_model,half_sib,no,narrow,authors,non_adult,adult,age at first reproduction (the interval between adult emergence and the first day of egg-laying),number of eggs laid during the first 5 days (early),reverse_maturation,fertility,include,cor,-0.495,0.219,se,NA,NA,NA,NA,NA,NA,Melbourne_28,table 3,maturation,fertility,family,-0.542661528,81,-1,0.542661528,female,cross,Insecta,between
1279,Epiphyas postvittana,246,rayyan-197247412,Genetic variation in the life-history traits of Epiphyas postvittana: Population structure and local adaptation,2000,NA,"Canberra, Australia",lab,both,female,96,96,NA,NA,96,96,32,32,339,339,animal_model,half_sib,no,narrow,authors,adult,both,body weight on the day of emergence,adult lifespan,size,survival,include,cor,0.55,0.208,se,NA,NA,NA,NA,NA,NA,Canberra_23,table 2,size,survival,family,0.618381314,96,1,0.618381314,female,cross,Insecta,between
1280,Epiphyas postvittana,246,rayyan-197247412,Genetic variation in the life-history traits of Epiphyas postvittana: Population structure and local adaptation,2000,NA,"Canberra, Australia",lab,both,female,96,96,NA,NA,96,96,32,32,339,339,animal_model,half_sib,no,narrow,authors,adult,non_adult,body weight on the day of emergence,age at first reproduction (the interval between adult emergence and the first day of egg-laying),size,reverse_maturation,include,cor,NA,0.202,se,NA,NA,NA,NA,NA,NA,Canberra_23,table 2,size,maturation,family,NA,96,-1,NA,female,cross,Insecta,between
1281,Epiphyas postvittana,246,rayyan-197247412,Genetic variation in the life-history traits of Epiphyas postvittana: Population structure and local adaptation,2000,NA,"Canberra, Australia",lab,both,both,96,96,NA,NA,96,96,32,32,339,339,animal_model,half_sib,no,narrow,authors,non_adult,adult,development time,total fecundity,reverse_maturation,fertility,include,cor,0.112,0.18,se,NA,NA,NA,NA,NA,NA,Canberra_23,table 2,maturation,fertility,family,0.112471866,96,-1,-0.112471866,both,cross,Insecta,between
1282,Epiphyas postvittana,246,rayyan-197247412,Genetic variation in the life-history traits of Epiphyas postvittana: Population structure and local adaptation,2000,NA,"Melbourne, Australia",lab,both,both,81,81,NA,NA,81,81,27,27,289,289,animal_model,half_sib,no,narrow,authors,non_adult,both,development time,adult lifespan,reverse_maturation,survival,include,cor,0.449,0.233,se,NA,NA,NA,NA,NA,NA,Melbourne_28,table 3,maturation,survival,family,0.483447067,81,-1,-0.483447067,both,cross,Insecta,between
1283,Epiphyas postvittana,246,rayyan-197247412,Genetic variation in the life-history traits of Epiphyas postvittana: Population structure and local adaptation,2000,NA,"Melbourne, Australia",lab,both,female,81,81,NA,NA,81,81,27,27,289,289,animal_model,half_sib,no,narrow,authors,non_adult,non_adult,development time,age at first reproduction (the interval between adult emergence and the first day of egg-laying),reverse_maturation,reverse_maturation,include,cor,0.358,0.187,se,NA,NA,NA,NA,NA,NA,Melbourne_28,table 3,maturation,maturation,family,0.374590002,81,1,0.374590002,female,non_adult,Insecta,within
1284,Epiphyas postvittana,246,rayyan-197247412,Genetic variation in the life-history traits of Epiphyas postvittana: Population structure and local adaptation,2000,NA,"Canberra, Australia",lab,both,female,96,96,NA,NA,96,96,32,32,339,339,animal_model,half_sib,no,narrow,authors,both,adult,adult lifespan,total fecundity,survival,fertility,include,cor,-0.299,0.288,se,NA,NA,NA,NA,NA,NA,Canberra_23,table 2,survival,fertility,family,-0.308421065,96,1,-0.308421065,female,cross,Insecta,between
1285,Epiphyas postvittana,246,rayyan-197247412,Genetic variation in the life-history traits of Epiphyas postvittana: Population structure and local adaptation,2000,NA,"Melbourne, Australia",lab,both,female,81,81,NA,NA,81,81,27,27,291,291,animal_model,half_sib,no,narrow,authors,both,non_adult,adult lifespan,age at first reproduction (the interval between adult emergence and the first day of egg-laying),survival,reverse_maturation,include,cor,0.087,0.237,se,NA,NA,NA,NA,NA,NA,Melbourne_23,table 2,survival,maturation,family,0.087220503,81,-1,-0.087220503,female,cross,Insecta,between
1286,Epiphyas postvittana,246,rayyan-197247412,Genetic variation in the life-history traits of Epiphyas postvittana: Population structure and local adaptation,2000,NA,"Melbourne, Australia",lab,both,female,81,81,NA,NA,81,81,27,27,289,289,animal_model,half_sib,no,narrow,authors,adult,both,body weight on the day of emergence,adult lifespan,size,survival,include,cor,-0.072,0.204,se,NA,NA,NA,NA,NA,NA,Melbourne_28,table 3,size,survival,family,-0.072124804,81,1,-0.072124804,female,cross,Insecta,between
1287,Epiphyas postvittana,246,rayyan-197247412,Genetic variation in the life-history traits of Epiphyas postvittana: Population structure and local adaptation,2000,NA,"Melbourne, Australia",lab,female,female,81,81,NA,NA,81,81,27,27,291,291,animal_model,half_sib,no,narrow,authors,adult,adult,number of eggs laid during the first 5 days (early),total fecundity,fertility,fertility,include,cor,0.336,0.325,se,NA,NA,NA,NA,NA,NA,Melbourne_23,table 2,fertility,fertility,family,0.349576602,81,1,0.349576602,female,adult,Insecta,within
1288,Epiphyas postvittana,246,rayyan-197247412,Genetic variation in the life-history traits of Epiphyas postvittana: Population structure and local adaptation,2000,NA,"Canberra, Australia",lab,both,both,96,96,NA,NA,96,96,32,32,335,335,animal_model,half_sib,no,narrow,authors,non_adult,adult,development time,body weight on the day of emergence,reverse_maturation,size,include,cor,0.464,0.174,se,NA,NA,NA,NA,NA,NA,Canberra_28,table 3,maturation,size,family,0.502396767,96,-1,-0.502396767,both,cross,Insecta,between
1289,Epiphyas postvittana,246,rayyan-197247412,Genetic variation in the life-history traits of Epiphyas postvittana: Population structure and local adaptation,2000,NA,"Melbourne, Australia",lab,both,both,81,81,NA,NA,81,81,27,27,291,291,animal_model,half_sib,no,narrow,authors,non_adult,both,development time,adult lifespan,reverse_maturation,survival,include,cor,0.15,0.235,se,NA,NA,NA,NA,NA,NA,Melbourne_23,table 2,maturation,survival,family,0.151140436,81,-1,-0.151140436,both,cross,Insecta,between
1290,Epiphyas postvittana,246,rayyan-197247412,Genetic variation in the life-history traits of Epiphyas postvittana: Population structure and local adaptation,2000,NA,"Canberra, Australia",lab,both,both,96,96,NA,NA,96,96,32,32,339,339,animal_model,half_sib,no,narrow,authors,non_adult,adult,development time,body weight on the day of emergence,reverse_maturation,size,include,cor,0.54,0.263,se,NA,NA,NA,NA,NA,NA,Canberra_23,table 2,maturation,size,family,0.604155603,96,-1,-0.604155603,both,cross,Insecta,between
1291,Epiphyas postvittana,246,rayyan-197247412,Genetic variation in the life-history traits of Epiphyas postvittana: Population structure and local adaptation,2000,NA,"Melbourne, Australia",lab,both,female,81,81,NA,NA,81,81,27,27,291,291,animal_model,half_sib,no,narrow,authors,non_adult,non_adult,development time,age at first reproduction (the interval between adult emergence and the first day of egg-laying),reverse_maturation,reverse_maturation,include,cor,0.261,0.192,se,NA,NA,NA,NA,NA,NA,Melbourne_23,table 2,maturation,maturation,family,0.267181208,81,1,0.267181208,female,non_adult,Insecta,within
1292,Epiphyas postvittana,246,rayyan-197247412,Genetic variation in the life-history traits of Epiphyas postvittana: Population structure and local adaptation,2000,NA,"Melbourne, Australia",lab,both,female,81,81,NA,NA,81,81,27,27,289,289,animal_model,half_sib,no,narrow,authors,both,adult,adult lifespan,total fecundity,survival,fertility,include,cor,0.745,0.263,se,NA,NA,NA,NA,NA,NA,Melbourne_28,table 3,survival,fertility,family,0.961623145,81,1,0.961623145,female,cross,Insecta,between
1293,Epiphyas postvittana,246,rayyan-197247412,Genetic variation in the life-history traits of Epiphyas postvittana: Population structure and local adaptation,2000,NA,"Canberra, Australia",lab,both,female,96,96,NA,NA,96,96,32,32,339,339,animal_model,half_sib,no,narrow,authors,non_adult,adult,development time,number of eggs laid during the first 5 days (early),reverse_maturation,fertility,include,cor,-0.343,0.183,se,NA,NA,NA,NA,NA,NA,Canberra_23,table 2,maturation,fertility,family,-0.357488589,96,-1,0.357488589,female,cross,Insecta,between
1294,Epiphyas postvittana,246,rayyan-197247412,Genetic variation in the life-history traits of Epiphyas postvittana: Population structure and local adaptation,2000,NA,"Canberra, Australia",lab,female,female,96,96,NA,NA,96,96,32,32,335,335,animal_model,half_sib,no,narrow,authors,non_adult,adult,age at first reproduction (the interval between adult emergence and the first day of egg-laying),total fecundity,reverse_maturation,fertility,include,cor,-0.761,0.219,se,NA,NA,NA,NA,NA,NA,Canberra_28,table 3,maturation,fertility,family,-0.998586778,96,-1,0.998586778,female,cross,Insecta,between
1295,Epiphyas postvittana,246,rayyan-197247412,Genetic variation in the life-history traits of Epiphyas postvittana: Population structure and local adaptation,2000,NA,"Canberra, Australia",lab,both,female,96,96,NA,NA,96,96,32,32,335,335,animal_model,half_sib,no,narrow,authors,non_adult,adult,development time,number of eggs laid during the first 5 days (early),reverse_maturation,fertility,include,cor,0.569,0.272,se,NA,NA,NA,NA,NA,NA,Canberra_28,table 3,maturation,fertility,family,0.646042831,96,-1,-0.646042831,female,cross,Insecta,between
1296,Epiphyas postvittana,246,rayyan-197247412,Genetic variation in the life-history traits of Epiphyas postvittana: Population structure and local adaptation,2000,NA,"Canberra, Australia",lab,both,both,96,96,NA,NA,96,96,32,32,335,335,animal_model,half_sib,no,narrow,authors,non_adult,adult,development time,total fecundity,reverse_maturation,fertility,include,cor,0.022,0.166,se,NA,NA,NA,NA,NA,NA,Canberra_28,table 3,maturation,fertility,family,0.02200355,96,-1,-0.02200355,both,cross,Insecta,between
1297,Epiphyas postvittana,246,rayyan-197247412,Genetic variation in the life-history traits of Epiphyas postvittana: Population structure and local adaptation,2000,NA,"Melbourne, Australia",lab,both,female,81,81,NA,NA,81,81,27,27,289,289,animal_model,half_sib,no,narrow,authors,non_adult,adult,development time,number of eggs laid during the first 5 days (early),reverse_maturation,fertility,include,cor,-0.485,0.218,se,NA,NA,NA,NA,NA,NA,Melbourne_28,table 3,maturation,fertility,family,-0.529501575,81,-1,0.529501575,female,cross,Insecta,between
1298,Epiphyas postvittana,246,rayyan-197247412,Genetic variation in the life-history traits of Epiphyas postvittana: Population structure and local adaptation,2000,NA,"Melbourne, Australia",lab,both,both,81,81,NA,NA,81,81,27,27,289,289,animal_model,half_sib,no,narrow,authors,non_adult,adult,development time,total fecundity,reverse_maturation,fertility,include,cor,-0.574,0.278,se,NA,NA,NA,NA,NA,NA,Melbourne_28,table 3,maturation,fertility,family,-0.653468041,81,-1,0.653468041,both,cross,Insecta,between
1299,Epiphyas postvittana,246,rayyan-197247412,Genetic variation in the life-history traits of Epiphyas postvittana: Population structure and local adaptation,2000,NA,"Canberra, Australia",lab,both,female,96,96,NA,NA,96,96,32,32,335,335,animal_model,half_sib,no,narrow,authors,adult,both,body weight on the day of emergence,adult lifespan,size,survival,include,cor,0.174,0.264,se,NA,NA,NA,NA,NA,NA,Canberra_28,table 3,size,survival,family,0.175788613,96,1,0.175788613,female,cross,Insecta,between
1300,Epiphyas postvittana,246,rayyan-197247412,Genetic variation in the life-history traits of Epiphyas postvittana: Population structure and local adaptation,2000,NA,"Melbourne, Australia",lab,female,female,81,81,NA,NA,81,81,27,27,291,291,animal_model,half_sib,no,narrow,authors,non_adult,adult,age at first reproduction (the interval between adult emergence and the first day of egg-laying),number of eggs laid during the first 5 days (early),reverse_maturation,fertility,include,cor,-0.348,0.213,se,NA,NA,NA,NA,NA,NA,Melbourne_23,table 2,maturation,fertility,family,-0.363166365,81,-1,0.363166365,female,cross,Insecta,between
1301,Epiphyas postvittana,246,rayyan-197247412,Genetic variation in the life-history traits of Epiphyas postvittana: Population structure and local adaptation,2000,NA,"Melbourne, Australia",lab,both,female,81,81,NA,NA,81,81,27,27,289,289,animal_model,half_sib,no,narrow,authors,adult,non_adult,body weight on the day of emergence,age at first reproduction (the interval between adult emergence and the first day of egg-laying),size,reverse_maturation,include,cor,0.023,0.224,se,NA,NA,NA,NA,NA,NA,Melbourne_28,table 3,size,maturation,family,0.023004057,81,-1,-0.023004057,female,cross,Insecta,between
1302,Epiphyas postvittana,246,rayyan-197247412,Genetic variation in the life-history traits of Epiphyas postvittana: Population structure and local adaptation,2000,NA,"Canberra, Australia",lab,female,female,96,96,NA,NA,96,96,32,32,339,339,animal_model,half_sib,no,narrow,authors,adult,adult,number of eggs laid during the first 5 days (early),total fecundity,fertility,fertility,include,cor,0.412,0.151,se,NA,NA,NA,NA,NA,NA,Canberra_23,table 2,fertility,fertility,family,0.438017735,96,1,0.438017735,female,adult,Insecta,within
1303,Epiphyas postvittana,246,rayyan-197247412,Genetic variation in the life-history traits of Epiphyas postvittana: Population structure and local adaptation,2000,NA,"Melbourne, Australia",lab,both,both,81,81,NA,NA,81,81,27,27,291,291,animal_model,half_sib,no,narrow,authors,non_adult,adult,development time,body weight on the day of emergence,reverse_maturation,size,include,cor,0.322,0.144,se,NA,NA,NA,NA,NA,NA,Melbourne_23,table 2,maturation,size,family,0.333876866,81,-1,-0.333876866,both,cross,Insecta,between
1304,Epiphyas postvittana,246,rayyan-197247412,Genetic variation in the life-history traits of Epiphyas postvittana: Population structure and local adaptation,2000,NA,"Canberra, Australia",lab,both,female,96,96,NA,NA,96,96,32,32,335,335,animal_model,half_sib,no,narrow,authors,both,adult,adult lifespan,total fecundity,survival,fertility,include,cor,0.928,0.333,se,NA,NA,NA,NA,NA,NA,Canberra_28,table 3,survival,fertility,family,1.643786178,96,1,1.643786178,female,cross,Insecta,between
1305,Epiphyas postvittana,246,rayyan-197247412,Genetic variation in the life-history traits of Epiphyas postvittana: Population structure and local adaptation,2000,NA,"Canberra, Australia",lab,both,female,96,96,NA,NA,96,96,32,32,339,339,animal_model,half_sib,no,narrow,authors,non_adult,non_adult,development time,age at first reproduction (the interval between adult emergence and the first day of egg-laying),reverse_maturation,reverse_maturation,include,cor,0.955,0.172,se,NA,NA,NA,NA,NA,NA,Canberra_23,table 2,maturation,maturation,family,1.885741491,96,1,1.885741491,female,non_adult,Insecta,within
1306,Epiphyas postvittana,246,rayyan-197247412,Genetic variation in the life-history traits of Epiphyas postvittana: Population structure and local adaptation,2000,NA,"Melbourne, Australia",lab,both,female,81,81,NA,NA,81,81,27,27,289,289,animal_model,half_sib,no,narrow,authors,both,adult,adult lifespan,number of eggs laid during the first 5 days (early),survival,fertility,include,cor,-0.349,0.259,se,NA,NA,NA,NA,NA,NA,Melbourne_28,table 3,survival,fertility,family,-0.364304607,81,1,-0.364304607,female,cross,Insecta,between
1307,Epiphyas postvittana,246,rayyan-197247412,Genetic variation in the life-history traits of Epiphyas postvittana: Population structure and local adaptation,2000,NA,"Canberra, Australia",lab,both,female,96,96,NA,NA,96,96,32,32,335,335,animal_model,half_sib,no,narrow,authors,adult,adult,body weight on the day of emergence,total fecundity,size,fertility,include,cor,0.833,0.257,se,NA,NA,NA,NA,NA,NA,Canberra_28,table 3,size,fertility,family,1.197857718,96,1,1.197857718,female,adult,Insecta,between
1308,Epiphyas postvittana,246,rayyan-197247412,Genetic variation in the life-history traits of Epiphyas postvittana: Population structure and local adaptation,2000,NA,"Melbourne, Australia",lab,both,both,81,81,NA,NA,81,81,27,27,289,289,animal_model,half_sib,no,narrow,authors,non_adult,adult,development time,body weight on the day of emergence,reverse_maturation,size,include,cor,0.215,0.103,se,NA,NA,NA,NA,NA,NA,Melbourne_28,table 3,maturation,size,family,0.218407819,81,-1,-0.218407819,both,cross,Insecta,between
1309,Epiphyas postvittana,246,rayyan-197247412,Genetic variation in the life-history traits of Epiphyas postvittana: Population structure and local adaptation,2000,NA,"Canberra, Australia",lab,both,female,96,96,NA,NA,96,96,32,32,335,335,animal_model,half_sib,no,narrow,authors,adult,non_adult,body weight on the day of emergence,age at first reproduction (the interval between adult emergence and the first day of egg-laying),size,reverse_maturation,include,cor,-0.268,0.156,se,NA,NA,NA,NA,NA,NA,Canberra_28,table 3,size,maturation,family,-0.274707811,96,-1,0.274707811,female,cross,Insecta,between
1310,Epiphyas postvittana,246,rayyan-197247412,Genetic variation in the life-history traits of Epiphyas postvittana: Population structure and local adaptation,2000,NA,"Canberra, Australia",lab,both,female,96,96,NA,NA,96,96,32,32,335,335,animal_model,half_sib,no,narrow,authors,adult,adult,body weight on the day of emergence,number of eggs laid during the first 5 days (early),size,fertility,include,cor,0.158,0.256,se,NA,NA,NA,NA,NA,NA,Canberra_28,table 3,size,fertility,family,0.159334822,96,1,0.159334822,female,adult,Insecta,between
1311,Epiphyas postvittana,246,rayyan-197247412,Genetic variation in the life-history traits of Epiphyas postvittana: Population structure and local adaptation,2000,NA,"Canberra, Australia",lab,female,female,96,96,NA,NA,96,96,32,32,335,335,animal_model,half_sib,no,narrow,authors,non_adult,adult,age at first reproduction (the interval between adult emergence and the first day of egg-laying),number of eggs laid during the first 5 days (early),reverse_maturation,fertility,include,cor,-0.506,0.177,se,NA,NA,NA,NA,NA,NA,Canberra_28,table 3,maturation,fertility,family,-0.557338446,96,-1,0.557338446,female,cross,Insecta,between
1312,Epiphyas postvittana,246,rayyan-197247412,Genetic variation in the life-history traits of Epiphyas postvittana: Population structure and local adaptation,2000,NA,"Canberra, Australia",lab,both,female,96,96,NA,NA,96,96,32,32,335,335,animal_model,half_sib,no,narrow,authors,both,non_adult,adult lifespan,age at first reproduction (the interval between adult emergence and the first day of egg-laying),survival,reverse_maturation,include,cor,0.285,0.152,se,NA,NA,NA,NA,NA,NA,Canberra_28,table 3,survival,maturation,family,0.293115727,96,-1,-0.293115727,female,cross,Insecta,between
1313,Epiphyas postvittana,246,rayyan-197247412,Genetic variation in the life-history traits of Epiphyas postvittana: Population structure and local adaptation,2000,NA,"Canberra, Australia",lab,both,female,96,96,NA,NA,96,96,32,32,335,335,animal_model,half_sib,no,narrow,authors,both,adult,adult lifespan,number of eggs laid during the first 5 days (early),survival,fertility,include,cor,NA,0.317,se,NA,NA,NA,NA,NA,NA,Canberra_28,table 3,survival,fertility,family,NA,96,1,NA,female,cross,Insecta,between
1314,Epiphyas postvittana,246,rayyan-197247412,Genetic variation in the life-history traits of Epiphyas postvittana: Population structure and local adaptation,2000,NA,"Melbourne, Australia",lab,both,female,81,81,NA,NA,81,81,27,27,289,289,animal_model,half_sib,no,narrow,authors,adult,adult,body weight on the day of emergence,number of eggs laid during the first 5 days (early),size,fertility,include,cor,0.132,0.147,se,NA,NA,NA,NA,NA,NA,Melbourne_28,table 3,size,fertility,family,0.132774772,81,1,0.132774772,female,adult,Insecta,between
1315,Epiphyas postvittana,246,rayyan-197247412,Genetic variation in the life-history traits of Epiphyas postvittana: Population structure and local adaptation,2000,NA,"Canberra, Australia",lab,female,female,96,96,NA,NA,96,96,32,32,335,335,animal_model,half_sib,no,narrow,authors,adult,adult,number of eggs laid during the first 5 days (early),total fecundity,fertility,fertility,include,cor,NA,0.322,se,NA,NA,NA,NA,NA,NA,Canberra_28,table 3,fertility,fertility,family,NA,96,1,NA,female,adult,Insecta,within
1316,Epiphyas postvittana,246,rayyan-197247412,Genetic variation in the life-history traits of Epiphyas postvittana: Population structure and local adaptation,2000,NA,"Canberra, Australia",lab,female,female,96,96,NA,NA,96,96,32,32,339,339,animal_model,half_sib,no,narrow,authors,non_adult,adult,age at first reproduction (the interval between adult emergence and the first day of egg-laying),total fecundity,reverse_maturation,fertility,include,cor,-0.559,0.151,se,NA,NA,NA,NA,NA,NA,Canberra_23,table 2,maturation,fertility,family,-0.631377497,96,-1,0.631377497,female,cross,Insecta,between
1317,Eurema hecabe,310,rayyan-697472393,Genotype-environment interaction reveals varied developmental responses to unpredictable host phenology in a tropical insect,2021,2017,"Cairns, Australia",lab,both,both,42,42,NA,NA,42,42,NA,NA,271,271,animal_model,full_sib,no,broad,authors,non_adult,adult,development time,adult body weight,reverse_maturation,size,include,cor,-0.195,0.283,se,NA,NA,NA,NA,NA,NA,HQ_dry,table 2,maturation,size,family,-0.197529593,42,-1,0.197529593,both,cross,Insecta,between
1318,Eurema hecabe,310,rayyan-697472393,Genotype-environment interaction reveals varied developmental responses to unpredictable host phenology in a tropical insect,2021,2017,"Cairns, Australia",lab,both,both,42,42,NA,NA,42,42,NA,NA,287,287,animal_model,full_sib,no,broad,authors,non_adult,adult,development time,adult body weight,reverse_maturation,size,include,cor,0.456,0.207,se,NA,NA,NA,NA,NA,NA,HQ_wet,table 2,maturation,size,family,0.492249491,42,-1,-0.492249491,both,cross,Insecta,between
1319,Eurema hecabe,310,rayyan-697472393,Genotype-environment interaction reveals varied developmental responses to unpredictable host phenology in a tropical insect,2021,2017,"Cairns, Australia",lab,both,both,42,42,NA,NA,42,42,NA,NA,403,397,animal_model,full_sib,no,broad,authors,non_adult,adult,development time,adult body weight,reverse_maturation,size,include,cor,-0.213,0.27,se,NA,NA,NA,NA,NA,NA,LQ_wet,table 2,maturation,size,family,-0.21631183,42,-1,0.21631183,both,cross,Insecta,between
1321,Ficedula albicollis,22,rayyan-687940443,Natural selection and inheritance of breeding time and clutch size in the collared flycatcher,2003,1980-1998,Swedish island of Gotland,field,female,female,NA,NA,NA,NA,NA,NA,NA,NA,1909,4544,animal_model,pedigree,no,narrow,authors,adult,adult,tarsus length,clutch size,size,fertility,include,cor,0.205,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-687940443,table 1,size,fertility,pedigree,0.207946366,1909,1,0.207946366,female,adult,Aves,between
1323,Folsomia candida,383,rayyan-697472922,"Reproductive flexibility: Genetic variation, genetic costs and long-term evolution in a collembola",2008,NA,NA,lab,female,female,NA,NA,11,11,NA,NA,NA,NA,110,110,animal_model,genetic_line,no,broad,authors,adult,adult,clutch size,reproductive investment,fertility,fertility,include,cor,0.84,"[0.49, 0.96]",95CI,NA,NA,NA,NA,NA,NA,P2_(day_7_onward),paragraph 2 in How do reproductive adjustments vary among individuals?,fertility,fertility,genotype,1.221173518,11,1,1.221173518,female,adult,Collembola,within
1324,Folsomia candida,383,rayyan-697472922,"Reproductive flexibility: Genetic variation, genetic costs and long-term evolution in a collembola",2008,NA,NA,lab,female,female,NA,NA,11,11,NA,NA,NA,NA,3377,110,animal_model,genetic_line,no,broad,authors,non_adult,adult,egg size,clutch size,size,fertility,include,cor,0.7,"[0.18, 0.92]",95CI,NA,NA,NA,NA,NA,NA,P2_(day_7_onward),paragraph 2 in How do reproductive adjustments vary among individuals?,size,fertility,genotype,0.867300528,11,1,0.867300528,female,cross,Collembola,between
1325,Folsomia candida,383,rayyan-697472922,"Reproductive flexibility: Genetic variation, genetic costs and long-term evolution in a collembola",2008,NA,NA,lab,female,female,NA,NA,11,11,NA,NA,NA,NA,110,110,animal_model,genetic_line,no,broad,authors,adult,adult,clutch size,reproductive investment,fertility,fertility,include,cor,-0.18,"[-0.75, 0.55]",95CI,NA,NA,NA,NA,NA,NA,P1_(day_1_day_6),paragraph 2 in How do reproductive adjustments vary among individuals?,fertility,fertility,genotype,-0.181982689,11,1,-0.181982689,female,adult,Collembola,within
1326,Folsomia candida,383,rayyan-697472922,"Reproductive flexibility: Genetic variation, genetic costs and long-term evolution in a collembola",2008,NA,NA,lab,female,female,NA,NA,11,11,NA,NA,NA,NA,3377,110,animal_model,genetic_line,no,broad,authors,non_adult,adult,egg size,reproductive investment,size,fertility,include,cor,0.87,"[0.56, 0.96]",95CI,NA,NA,NA,NA,NA,NA,P2_(day_7_onward),paragraph 2 in How do reproductive adjustments vary among individuals?,size,fertility,genotype,1.33307963,11,1,1.33307963,female,cross,Collembola,between
1327,Folsomia candida,383,rayyan-697472922,"Reproductive flexibility: Genetic variation, genetic costs and long-term evolution in a collembola",2008,NA,NA,lab,female,female,NA,NA,11,11,NA,NA,NA,NA,3377,110,animal_model,genetic_line,no,broad,authors,non_adult,adult,egg size,reproductive investment,size,fertility,include,cor,0.14,"[-0.5, 0.68]",95CI,NA,NA,NA,NA,NA,NA,P1_(day_1_day_6),paragraph 2 in How do reproductive adjustments vary among individuals?,size,fertility,genotype,0.140925576,11,1,0.140925576,female,cross,Collembola,between
1328,Folsomia candida,383,rayyan-697472922,"Reproductive flexibility: Genetic variation, genetic costs and long-term evolution in a collembola",2008,NA,NA,lab,female,female,NA,NA,11,11,NA,NA,NA,NA,3377,220,animal_model,genetic_line,no,broad,authors,non_adult,both,egg size,mortality risk (clone AP as ref),size,reverse_survival,include,cor,0.79,"[0.37, 0.94]",95CI,NA,NA,NA,NA,NA,NA,rayyan-697472922,paragraph 3 in Genetic variation in reproductive flexibility,size,survival,genotype,1.071431684,11,-1,-1.071431684,female,cross,Collembola,between
1329,Folsomia candida,383,rayyan-697472922,"Reproductive flexibility: Genetic variation, genetic costs and long-term evolution in a collembola",2008,NA,NA,lab,female,female,NA,NA,11,11,NA,NA,NA,NA,3377,110,animal_model,genetic_line,no,broad,authors,non_adult,adult,egg size,clutch size,size,fertility,include,cor,-0.81,"[-0.96, -0.31]",95CI,NA,NA,NA,NA,NA,NA,P1_(day_1_day_6),paragraph 2 in How do reproductive adjustments vary among individuals?,size,fertility,genotype,-1.127029026,11,1,-1.127029026,female,cross,Collembola,between
1332,Gryllodes sigillatus,348,rayyan-697472739,Sexual selection affects the evolution of lifespan and ageing in the decorated cricket gryllodes sigillatus,2012,2001,"Las Cruces, New Mexico",lab,female,female,NA,NA,8,8,NA,NA,NA,NA,727,664,matrix,genetic_line,no,broad,authors,both,adult,baseline mortality,mid life reproductive effort (female fecundity),reverse_survival,fertility,include,cor,-0.99,0.46,se,NA,NA,NA,NA,NA,NA,female,table 4,survival,fertility,genotype,-2.646652412,8,-1,2.646652412,female,cross,Insecta,between
1336,Gryllodes sigillatus,348,rayyan-697472739,Sexual selection affects the evolution of lifespan and ageing in the decorated cricket gryllodes sigillatus,2012,2001,"Las Cruces, New Mexico",lab,male,male,NA,NA,8,8,NA,NA,NA,NA,808,808,matrix,genetic_line,no,broad,authors,both,both,adult lifespan,baseline mortality,survival,reverse_survival,include,cor,-0.79,0.03,se,NA,NA,NA,NA,NA,NA,male,table 4,survival,survival,genotype,-1.071431684,8,-1,1.071431684,male,both,Insecta,within
1343,Gryllodes sigillatus,348,rayyan-697472739,Sexual selection affects the evolution of lifespan and ageing in the decorated cricket gryllodes sigillatus,2012,2001,"Las Cruces, New Mexico",lab,female,female,NA,NA,8,8,NA,NA,NA,NA,770,559,matrix,genetic_line,no,broad,authors,adult,adult,early life reproductive effort (female fecundity),late life reproductive effort (female fecundity),fertility,fertility,include,cor,0.34,0.21,se,NA,NA,NA,NA,NA,NA,female,table 4,fertility,fertility,genotype,0.354092529,8,1,0.354092529,female,adult,Insecta,within
1345,Gryllodes sigillatus,348,rayyan-697472739,Sexual selection affects the evolution of lifespan and ageing in the decorated cricket gryllodes sigillatus,2012,2001,"Las Cruces, New Mexico",lab,female,female,NA,NA,8,8,NA,NA,NA,NA,727,559,matrix,genetic_line,no,broad,authors,both,adult,baseline mortality,late life reproductive effort (female fecundity),reverse_survival,fertility,include,cor,-0.02,0.04,se,NA,NA,NA,NA,NA,NA,female,table 4,survival,fertility,genotype,-0.020002667,8,-1,0.020002667,female,cross,Insecta,between
1347,Gryllodes sigillatus,348,rayyan-697472739,Sexual selection affects the evolution of lifespan and ageing in the decorated cricket gryllodes sigillatus,2012,2001,"Las Cruces, New Mexico",lab,female,female,NA,NA,8,8,NA,NA,NA,NA,727,664,matrix,genetic_line,no,broad,authors,both,adult,adult lifespan,mid life reproductive effort (female fecundity),survival,fertility,include,cor,0.32,0.09,se,NA,NA,NA,NA,NA,NA,female,table 4,survival,fertility,genotype,0.331647109,8,1,0.331647109,female,cross,Insecta,between
1348,Gryllodes sigillatus,348,rayyan-697472739,Sexual selection affects the evolution of lifespan and ageing in the decorated cricket gryllodes sigillatus,2012,2001,"Las Cruces, New Mexico",lab,female,female,NA,NA,8,8,NA,NA,NA,NA,727,727,matrix,genetic_line,no,broad,authors,both,both,adult lifespan,baseline mortality,survival,reverse_survival,include,cor,-0.4,0.03,se,NA,NA,NA,NA,NA,NA,female,table 4,survival,survival,genotype,-0.42364893,8,-1,0.42364893,female,both,Insecta,within
1352,Gryllodes sigillatus,348,rayyan-697472739,Sexual selection affects the evolution of lifespan and ageing in the decorated cricket gryllodes sigillatus,2012,2001,"Las Cruces, New Mexico",lab,female,female,NA,NA,8,8,NA,NA,NA,NA,727,559,matrix,genetic_line,no,broad,authors,both,adult,adult lifespan,late life reproductive effort (female fecundity),survival,fertility,include,cor,0.09,0.11,se,NA,NA,NA,NA,NA,NA,female,table 4,survival,fertility,genotype,0.090244188,8,1,0.090244188,female,cross,Insecta,between
1353,Gryllodes sigillatus,348,rayyan-697472739,Sexual selection affects the evolution of lifespan and ageing in the decorated cricket gryllodes sigillatus,2012,2001,"Las Cruces, New Mexico",lab,female,female,NA,NA,8,8,NA,NA,NA,NA,727,770,matrix,genetic_line,no,broad,authors,both,adult,baseline mortality,early life reproductive effort (female fecundity),reverse_survival,fertility,include,cor,-0.98,0.45,se,NA,NA,NA,NA,NA,NA,female,table 4,survival,fertility,genotype,-2.297559925,8,-1,2.297559925,female,cross,Insecta,between
1354,Gryllodes sigillatus,348,rayyan-697472739,Sexual selection affects the evolution of lifespan and ageing in the decorated cricket gryllodes sigillatus,2012,2001,"Las Cruces, New Mexico",lab,female,female,NA,NA,8,8,NA,NA,NA,NA,727,770,matrix,genetic_line,no,broad,authors,both,adult,adult lifespan,early life reproductive effort (female fecundity),survival,fertility,include,cor,-0.11,0.11,se,NA,NA,NA,NA,NA,NA,female,table 4,survival,fertility,genotype,-0.110446916,8,1,-0.110446916,female,cross,Insecta,between
1356,Gryllodes sigillatus,348,rayyan-697472739,Sexual selection affects the evolution of lifespan and ageing in the decorated cricket gryllodes sigillatus,2012,2001,"Las Cruces, New Mexico",lab,female,female,NA,NA,8,8,NA,NA,NA,NA,770,664,matrix,genetic_line,no,broad,authors,adult,adult,early life reproductive effort (female fecundity),mid life reproductive effort (female fecundity),fertility,fertility,include,cor,0.77,0.35,se,NA,NA,NA,NA,NA,NA,female,table 4,fertility,fertility,genotype,1.020327758,8,1,1.020327758,female,adult,Insecta,within
1357,Gryllodes sigillatus,348,rayyan-697472739,Sexual selection affects the evolution of lifespan and ageing in the decorated cricket gryllodes sigillatus,2012,2001,"Las Cruces, New Mexico",lab,female,female,NA,NA,8,8,NA,NA,NA,NA,664,559,matrix,genetic_line,no,broad,authors,adult,adult,mid life reproductive effort (female fecundity),late life reproductive effort (female fecundity),fertility,fertility,include,cor,0.17,0.05,se,NA,NA,NA,NA,NA,NA,female,table 4,fertility,fertility,genotype,0.171666664,8,1,0.171666664,female,adult,Insecta,within
1360,Gryllus bimaculatus,321,rayyan-697472507,Behavioural mediators of genetic life-history trade-offs: A test of the pace-of-life syndrome hypothesis in field crickets,2017,2013,Italy ,lab,male,male,68,68,NA,NA,100,100,50,50,451,330,animal_model,full_sib,no,narrow,authors,non_adult,both,developmental time,adult lifespan,reverse_maturation,survival,include,cor,0.43,0.24,se,NA,NA,NA,NA,NA,NA,rayyan-697472507,table s4,maturation,survival,family,0.459896681,68,-1,-0.459896681,male,cross,Insecta,between
1361,Gryllus bimaculatus,321,rayyan-697472507,Behavioural mediators of genetic life-history trade-offs: A test of the pace-of-life syndrome hypothesis in field crickets,2017,2013,Italy ,lab,male,male,68,68,NA,NA,100,100,50,50,451,371,animal_model,full_sib,no,narrow,authors,non_adult,adult,developmental time,size at maturity,reverse_maturation,size,include,cor,-0.05,0.23,se,NA,NA,NA,NA,NA,NA,rayyan-697472507,table s4,maturation,size,family,-0.050041729,68,-1,0.050041729,male,cross,Insecta,between
1362,Gryllus bimaculatus,321,rayyan-697472507,Behavioural mediators of genetic life-history trade-offs: A test of the pace-of-life syndrome hypothesis in field crickets,2017,2013,Italy ,lab,male,male,68,68,NA,NA,100,100,50,50,371,330,animal_model,full_sib,no,narrow,authors,adult,both,size at maturity,adult lifespan,size,survival,include,cor,0.29,0.24,se,NA,NA,NA,NA,NA,NA,rayyan-697472507,table s4,size,survival,family,0.298566264,68,1,0.298566264,male,cross,Insecta,between
1363,Gryllus bimaculatus,62,rayyan-697471526,Quantitative genetics of immunity and life history under different photoperiods,2012,NA,NA,lab,both,both,84,84,NA,NA,84,84,28,28,1104,1104,animal_model,full/half_sib,no,narrow,authors,non_adult,adult,time to reach adulthood,body size after 3 to 5 days in adulthood,reverse_maturation,size,include,cor,-0.174,0.222,se,NA,NA,NA,NA,NA,NA,rayyan-697471526,table 3,maturation,size,family,-0.175788613,84,-1,0.175788613,both,cross,Insecta,between
1366,Gryllus firmus,101,rayyan-697471782,Extra-nuclear effects on growth and development in the sand cricket Gryllus firmus,2004,1981,Florida,lab,both,both,1053,729,7,7,1053,729,1053,729,21060,14580,line_mean_correlation,genetic_line,no,broad,authors,non_adult,non_adult,development time,nymphal weight at 14 days,reverse_maturation,size,include_2,cor,-0.111,NA,NA,NA,NA,NA,NA,NA,NA,male_line,table 6,maturation,size,genotype,-0.111459277,7,-1,0.111459277,both,non_adult,Insecta,between
1367,Gryllus firmus,101,rayyan-697471782,Extra-nuclear effects on growth and development in the sand cricket Gryllus firmus,2004,1981,Florida,lab,both,both,1053,729,7,7,1053,729,1053,729,21060,14580,line_mean_correlation,genetic_line,no,broad,authors,non_adult,non_adult,development time,nymphal weight at 21 days,reverse_maturation,size,include_2,cor,-0.116,NA,NA,NA,NA,NA,NA,NA,NA,male_line,table 6,maturation,size,genotype,-0.11652454,7,-1,0.11652454,both,non_adult,Insecta,between
1368,Gryllus firmus,152,rayyan-697472319,Four characters in a trade-off: dissecting their phenotypic and genetic relations,1999,NA,NA,lab,female,female,66,66,NA,NA,66,66,22,22,679.8,679.8,animal_model,half_sib,no,broad,authors,adult,adult,eggs in the ovaries,eggs laid (early fecundity),fertility,fertility,include_2,cor,0.11,0.35,se,NA,NA,NA,NA,NA,NA,dam_random_effect,table 2,fertility,fertility,family,0.110446916,66,1,0.110446916,female,adult,Insecta,within
1371,Gryllus firmus,101,rayyan-697471782,Extra-nuclear effects on growth and development in the sand cricket Gryllus firmus,2004,1981,Florida,lab,both,both,1053,729,7,7,1053,729,1053,729,21060,14580,line_mean_correlation,genetic_line,no,broad,authors,non_adult,non_adult,development time,nymphal weight at 28 days,reverse_maturation,size,include_2,cor,-0.041,NA,NA,NA,NA,NA,NA,NA,NA,male_line,table 6,maturation,size,genotype,-0.041022997,7,-1,0.041022997,both,non_adult,Insecta,between
1372,Gryllus integer,54,rayyan-697471468,Personality pace-of-life hypothesis: Testing genetic associations among personality and life history,2013,NA,California ,lab,both,both,NA,NA,NA,NA,54,54,18,18,538,538,animal_model,full/half_sib,no,narrow,authors,adult,non_adult,body mass,maturation time,size,reverse_maturation,include,cor,0.52,0.142,se,NA,NA,NA,NA,NA,NA,rayyan-697471468,table 4,size,maturation,family,0.576339755,54,-1,-0.576339755,both,cross,Insecta,between
1373,Hyla regilla,398,rayyan-697473011,"A quantitative genetic test of adaptive decoupling across metamorphosis for locomotor and life-history traits in the pacific tree frog, Hyla regilla",2001,1996,"California, USA",lab,both,both,NA,NA,NA,NA,4,4,43,39,709,542,animal_model,full_sib,no,narrow,authors,non_adult,non_adult,larval period (time to stage 42),tail at stage 42,reverse_maturation,size,include,cor,0.4,0.51,se,NA,NA,NA,NA,NA,NA,rayyan-697473011,table 5,maturation,size,family,0.42364893,4,-1,-0.42364893,both,non_adult,Amphibia,between
1374,Hyla regilla,398,rayyan-697473011,"A quantitative genetic test of adaptive decoupling across metamorphosis for locomotor and life-history traits in the pacific tree frog, Hyla regilla",2001,1996,"California, USA",lab,both,both,NA,NA,NA,NA,4,4,43,45,709,612,animal_model,full_sib,no,narrow,authors,non_adult,non_adult,larval period (time to stage 42),wet mass as juvenile frog ,reverse_maturation,size,include,cor,0.54,0.4,se,NA,NA,NA,NA,NA,NA,rayyan-697473011,table 5,maturation,size,family,0.604155603,4,-1,-0.604155603,both,non_adult,Amphibia,between
1375,Hyla regilla,398,rayyan-697473011,"A quantitative genetic test of adaptive decoupling across metamorphosis for locomotor and life-history traits in the pacific tree frog, Hyla regilla",2001,1996,"California, USA",lab,both,both,NA,NA,NA,NA,4,4,43,41,709,562,animal_model,full_sib,no,narrow,authors,non_adult,non_adult,larval period (time to stage 42),svl length at stage 42,reverse_maturation,size,include,cor,NA,1.21,se,NA,NA,NA,NA,NA,NA,rayyan-697473011,table 5,maturation,size,family,NA,4,-1,NA,both,non_adult,Amphibia,between
1376,Lacerta vivipara,123,rayyan-697471864,Phenotypic plasticity of growth and survival in the common lizard Lacerta vivipara,1996,1994,"Lozere, France",lab,both,both,20,20,NA,NA,20,20,NA,NA,NA,NA,family_mean_correlation,half_sib,no,broad,CC,non_adult,non_adult,growth (hatching),survival (hatching),growth,survival,include,cor,-0.34,NA,NA,NA,NA,NA,NA,NA,NA,Brittany ,GENETIC CORRELATION BETWEEN GROWTH AND SURVIVAL,growth,survival,family,-0.354092529,20,1,-0.354092529,both,non_adult,Lepidosauria,between
1377,Lacerta vivipara,123,rayyan-697471864,Phenotypic plasticity of growth and survival in the common lizard Lacerta vivipara,1996,1994,"Lozere, France",lab,both,both,40,40,NA,NA,40,40,NA,NA,NA,NA,family_mean_correlation,half_sib,no,broad,CC,non_adult,non_adult,growth (hatching),survival (hatching),growth,survival,include,cor,0.166,NA,NA,NA,NA,NA,NA,NA,NA,Lozere,GENETIC CORRELATION BETWEEN GROWTH AND SURVIVAL,growth,survival,family,0.167550482,40,1,0.167550482,both,non_adult,Lepidosauria,between
1378,Lampropholis coggeri,161,rayyan-197246971,Heritability of climate-relevant traits in a rainforest skink,2019,2013-2014,"Hervey range, Australia",lab,both,both,51,51,NA,NA,33,33,30,30,152,152,animal_model,full/half_sib,no,narrow,authors,non_adult,non_adult,Snout ventral length of hatchling,tail length of hatchling,size,size,include,cor,0.752,0.161,se,NA,NA,NA,NA,NA,NA,rayyan-197246971,table 4,size,size,family,0.977542263,51,1,0.977542263,both,non_adult,Lepidosauria,within
1379,Lampropholis coggeri,161,rayyan-197246971,Heritability of climate-relevant traits in a rainforest skink,2019,2013-2014,"Hervey range, Australia",lab,both,both,51,51,NA,NA,33,33,30,30,152,152,animal_model,full/half_sib,no,narrow,authors,non_adult,non_adult,Mass of the hatchling,tail length of hatchling,size,size,include,cor,0.686,0.19,se,NA,NA,NA,NA,NA,NA,rayyan-197246971,table 4,size,size,family,0.840360576,51,1,0.840360576,both,non_adult,Lepidosauria,within
1380,Lampropholis coggeri,161,rayyan-197246971,Heritability of climate-relevant traits in a rainforest skink,2019,2013-2014,"Hervey range, Australia",lab,both,both,51,51,NA,NA,33,33,30,30,152,152,animal_model,full/half_sib,no,narrow,authors,non_adult,non_adult,Mass of the hatchling,Growth rate,size,growth,include,cor,0.202,0.465,se,NA,NA,NA,NA,NA,NA,rayyan-197246971,table 4,size,growth,family,0.204816759,51,1,0.204816759,both,non_adult,Lepidosauria,between
1381,Lampropholis coggeri,161,rayyan-197246971,Heritability of climate-relevant traits in a rainforest skink,2019,2013-2014,"Hervey range, Australia",lab,both,both,51,51,NA,NA,33,33,30,30,152,152,animal_model,full/half_sib,no,narrow,authors,non_adult,non_adult,Snout ventral length of hatchling,Growth rate,size,growth,include,cor,-0.253,0.434,se,NA,NA,NA,NA,NA,NA,rayyan-197246971,table 4,size,growth,family,-0.258615385,51,1,-0.258615385,both,non_adult,Lepidosauria,between
1382,Lampropholis coggeri,161,rayyan-197246971,Heritability of climate-relevant traits in a rainforest skink,2019,2013-2014,"Hervey range, Australia",lab,both,both,51,51,NA,NA,33,33,30,30,152,152,animal_model,full/half_sib,no,narrow,authors,non_adult,non_adult,tail length of hatchling,Growth rate,size,growth,include,cor,-0.349,0.43,se,NA,NA,NA,NA,NA,NA,rayyan-197246971,table 4,size,growth,family,-0.364304607,51,1,-0.364304607,both,non_adult,Lepidosauria,between
1383,Lampropholis coggeri,161,rayyan-197246971,Heritability of climate-relevant traits in a rainforest skink,2019,2013-2014,"Hervey range, Australia",lab,both,both,51,51,NA,NA,33,33,30,30,152,152,animal_model,full/half_sib,no,narrow,authors,non_adult,non_adult,Mass of the hatchling,Snout ventral length of hatchling,size,size,include,cor,0.867,0.13,se,NA,NA,NA,NA,NA,NA,rayyan-197246971,table 4,size,size,family,1.320869508,51,1,1.320869508,both,non_adult,Lepidosauria,within
1384,Lema daturaphila,33,rayyan-697471303,Enhanced survival of a specialized leaf beetle reveals potential trade-offs with host utilization traits,2019,NA,"Pedregal de San Ángel Reserve, Mexico",lab,both,both,25,25,NA,NA,25,25,25,25,250,250,family_mean_correlation,full_sib,yes,broad,CC,non_adult,adult,development time from egg hatching to imago emergence,adult mass at emergence,reverse_maturation,size,include,cov,0.095111967,"[-0.26, 0.47]",CI,0.91,"[0.44, 1.38]",CI,0.797,"[0.28, 1.33]",CI,selection,table 3,maturation,size,family,0.095400337,25,-1,-0.095400337,both,cross,Insecta,between
1385,Lema daturaphila,33,rayyan-697471303,Enhanced survival of a specialized leaf beetle reveals potential trade-offs with host utilization traits,2019,NA,"Pedregal de San Ángel Reserve, Mexico",lab,both,female,25,25,NA,NA,25,25,25,25,250,25,family_mean_correlation,full_sib,no,broad,CC,non_adult,adult,survival to sexual maturity,number of eggs laid per female,survival,fertility,include,cov,0.502429589,"[-0.08, 1.6]",CI,1.597,"[0.37, 3.6]",CI,0.846,"[0.36, 1.35]",CI,control,table 2,survival,fertility,family,0.552550863,25,1,0.552550863,female,cross,Insecta,between
1386,Lema daturaphila,33,rayyan-697471303,Enhanced survival of a specialized leaf beetle reveals potential trade-offs with host utilization traits,2019,NA,"Pedregal de San Ángel Reserve, Mexico",lab,both,both,25,25,NA,NA,25,25,25,25,250,250,family_mean_correlation,full_sib,no,broad,CC,non_adult,non_adult,relative growth rate of larvae,development time from egg hatching to imago emergence,growth,reverse_maturation,include,cov,-0.621316317,"[-0.92, -0.15]",CI,0.88,"[0.46, 1.27]",CI,0.91,"[0.44, 1.38]",CI,control,table 2,growth,maturation,family,-0.727146197,25,-1,0.727146197,both,non_adult,Insecta,between
1387,Lema daturaphila,33,rayyan-697471303,Enhanced survival of a specialized leaf beetle reveals potential trade-offs with host utilization traits,2019,NA,"Pedregal de San Ángel Reserve, Mexico",lab,both,both,25,25,NA,NA,25,25,25,25,250,250,family_mean_correlation,full_sib,yes,broad,CC,non_adult,non_adult,development time from egg hatching to imago emergence,survival to sexual maturity,reverse_maturation,survival,include,cov,-0.072168237,"[-0.36, 0.17]",CI,0.91,"[0.44, 1.38]",CI,1.597,"[0.37, 3.6]",CI,selection,table 3,maturation,survival,family,-0.072293921,25,-1,0.072293921,both,non_adult,Insecta,between
1388,Lema daturaphila,33,rayyan-697471303,Enhanced survival of a specialized leaf beetle reveals potential trade-offs with host utilization traits,2019,NA,"Pedregal de San Ángel Reserve, Mexico",lab,both,female,25,25,NA,NA,25,25,25,25,250,25,family_mean_correlation,full_sib,yes,broad,CC,non_adult,adult,relative growth rate of larvae,number of eggs laid per female,growth,fertility,include,cov,-0.81244038,"[-1.2, -0.21]",CI,0.88,"[0.46, 1.27]",CI,0.846,"[0.36, 1.35]",CI,selection,table 3,growth,fertility,family,-1.134166361,25,1,-1.134166361,female,cross,Insecta,between
1389,Lema daturaphila,33,rayyan-697471303,Enhanced survival of a specialized leaf beetle reveals potential trade-offs with host utilization traits,2019,NA,"Pedregal de San Ángel Reserve, Mexico",lab,both,both,25,25,NA,NA,25,25,25,25,250,250,family_mean_correlation,full_sib,yes,broad,CC,adult,non_adult,adult mass at emergence,survival to sexual maturity,size,survival,include,cov,0.039000579,"[-0.17, 0.24]",CI,0.797,"[0.28, 1.33]",CI,1.597,"[0.37, 3.6]",CI,selection,table 3,size,survival,family,0.039020371,25,1,0.039020371,both,cross,Insecta,between
1390,Lema daturaphila,33,rayyan-697471303,Enhanced survival of a specialized leaf beetle reveals potential trade-offs with host utilization traits,2019,NA,"Pedregal de San Ángel Reserve, Mexico",lab,both,female,25,25,NA,NA,25,25,25,25,250,25,family_mean_correlation,full_sib,yes,broad,CC,adult,adult,adult mass at emergence,number of eggs laid per female,size,fertility,include,cov,0.38239773,"[-0.21, 0.82]",CI,0.797,"[0.28, 1.33]",CI,0.846,"[0.36, 1.35]",CI,selection,table 3,size,fertility,family,0.402865041,25,1,0.402865041,female,adult,Insecta,between
1391,Lema daturaphila,33,rayyan-697471303,Enhanced survival of a specialized leaf beetle reveals potential trade-offs with host utilization traits,2019,NA,"Pedregal de San Ángel Reserve, Mexico",lab,both,female,25,25,NA,NA,25,25,25,25,250,25,family_mean_correlation,full_sib,yes,broad,CC,non_adult,adult,survival to sexual maturity,number of eggs laid per female,survival,fertility,include,cov,-0.270141936,"[-0.7, -0.01]",CI,1.597,"[0.37, 3.6]",CI,0.846,"[0.36, 1.35]",CI,selection,table 3,survival,fertility,family,-0.277016926,25,1,-0.277016926,female,cross,Insecta,between
1392,Lema daturaphila,33,rayyan-697471303,Enhanced survival of a specialized leaf beetle reveals potential trade-offs with host utilization traits,2019,NA,"Pedregal de San Ángel Reserve, Mexico",lab,both,female,25,25,NA,NA,25,25,25,25,250,25,family_mean_correlation,full_sib,no,broad,CC,adult,adult,adult mass at emergence,number of eggs laid per female,size,fertility,include,cov,-0.225298026,"[-0.65, 0.24]",CI,0.797,"[0.28, 1.33]",CI,0.846,"[0.36, 1.35]",CI,control,table 2,size,fertility,family,-0.229230487,25,1,-0.229230487,female,adult,Insecta,between
1393,Lema daturaphila,33,rayyan-697471303,Enhanced survival of a specialized leaf beetle reveals potential trade-offs with host utilization traits,2019,NA,"Pedregal de San Ángel Reserve, Mexico",lab,both,both,25,25,NA,NA,25,25,25,25,250,250,family_mean_correlation,full_sib,no,broad,CC,adult,non_adult,adult mass at emergence,survival to sexual maturity,size,survival,include,cov,-0.469779705,"[-1.34, 0]",CI,0.797,"[0.28, 1.33]",CI,1.597,"[0.37, 3.6]",CI,control,table 2,size,survival,family,-0.509787618,25,1,-0.509787618,both,cross,Insecta,between
1394,Lema daturaphila,33,rayyan-697471303,Enhanced survival of a specialized leaf beetle reveals potential trade-offs with host utilization traits,2019,NA,"Pedregal de San Ángel Reserve, Mexico",lab,both,both,25,25,NA,NA,25,25,25,25,250,250,family_mean_correlation,full_sib,yes,broad,CC,non_adult,non_adult,relative growth rate of larvae,survival to sexual maturity,growth,survival,include,cov,0.106286168,"[-0.15, 0.4]",CI,0.88,"[0.46, 1.27]",CI,1.597,"[0.37, 3.6]",CI,selection,table 3,growth,survival,family,0.106689133,25,1,0.106689133,both,non_adult,Insecta,between
1395,Lema daturaphila,33,rayyan-697471303,Enhanced survival of a specialized leaf beetle reveals potential trade-offs with host utilization traits,2019,NA,"Pedregal de San Ángel Reserve, Mexico",lab,both,female,25,25,NA,NA,25,25,25,25,250,25,family_mean_correlation,full_sib,no,broad,CC,non_adult,adult,relative growth rate of larvae,number of eggs laid per female,growth,fertility,include,cov,0.172687042,"[-0.21, 0.52]",CI,0.88,"[0.46, 1.27]",CI,0.846,"[0.36, 1.35]",CI,control,table 2,growth,fertility,family,0.174434981,25,1,0.174434981,female,cross,Insecta,between
1396,Lema daturaphila,33,rayyan-697471303,Enhanced survival of a specialized leaf beetle reveals potential trade-offs with host utilization traits,2019,NA,"Pedregal de San Ángel Reserve, Mexico",lab,both,female,25,25,NA,NA,25,25,25,25,250,25,family_mean_correlation,full_sib,yes,broad,CC,non_adult,adult,development time from egg hatching to imago emergence,number of eggs laid per female,reverse_maturation,fertility,include,cov,0.178934373,"[-0.22, 0.54]",CI,0.91,"[0.44, 1.38]",CI,0.846,"[0.36, 1.35]",CI,selection,table 3,maturation,fertility,family,0.180881597,25,-1,-0.180881597,female,cross,Insecta,between
1397,Lema daturaphila,33,rayyan-697471303,Enhanced survival of a specialized leaf beetle reveals potential trade-offs with host utilization traits,2019,NA,"Pedregal de San Ángel Reserve, Mexico",lab,both,both,25,25,NA,NA,25,25,25,25,250,250,family_mean_correlation,full_sib,no,broad,CC,non_adult,adult,relative growth rate of larvae,adult mass at emergence,growth,size,include,cov,-0.309263928,"[-0.42, -0.07]",CI,0.88,"[0.46, 1.27]",CI,0.797,"[0.28, 1.33]",CI,control,table 2,growth,size,family,-0.319731285,25,1,-0.319731285,both,cross,Insecta,between
1398,Lema daturaphila,33,rayyan-697471303,Enhanced survival of a specialized leaf beetle reveals potential trade-offs with host utilization traits,2019,NA,"Pedregal de San Ángel Reserve, Mexico",lab,both,both,25,25,NA,NA,25,25,25,25,250,250,family_mean_correlation,full_sib,no,broad,CC,non_adult,non_adult,relative growth rate of larvae,survival to sexual maturity,growth,survival,include,cov,0.284273323,"[-0.06, 0.74]",CI,0.88,"[0.46, 1.27]",CI,1.597,"[0.37, 3.6]",CI,control,table 2,growth,survival,family,0.292324986,25,1,0.292324986,both,non_adult,Insecta,between
1399,Lema daturaphila,33,rayyan-697471303,Enhanced survival of a specialized leaf beetle reveals potential trade-offs with host utilization traits,2019,NA,"Pedregal de San Ángel Reserve, Mexico",lab,both,both,25,25,NA,NA,25,25,25,25,250,250,family_mean_correlation,full_sib,yes,broad,CC,non_adult,non_adult,relative growth rate of larvae,development time from egg hatching to imago emergence,growth,reverse_maturation,include,cov,-0.545327991,"[-0.88, -0.06]",CI,0.88,"[0.46, 1.27]",CI,0.91,"[0.44, 1.38]",CI,selection,table 3,growth,maturation,family,-0.611707579,25,-1,0.611707579,both,non_adult,Insecta,between
1400,Lema daturaphila,33,rayyan-697471303,Enhanced survival of a specialized leaf beetle reveals potential trade-offs with host utilization traits,2019,NA,"Pedregal de San Ángel Reserve, Mexico",lab,both,female,25,25,NA,NA,25,25,25,25,250,25,family_mean_correlation,full_sib,no,broad,CC,non_adult,adult,development time from egg hatching to imago emergence,number of eggs laid per female,reverse_maturation,fertility,include,cov,-0.196030013,"[-0.57, 0.24]",CI,0.91,"[0.44, 1.38]",CI,0.846,"[0.36, 1.35]",CI,control,table 2,maturation,fertility,family,-0.198600545,25,-1,0.198600545,female,cross,Insecta,between
1401,Lema daturaphila,33,rayyan-697471303,Enhanced survival of a specialized leaf beetle reveals potential trade-offs with host utilization traits,2019,NA,"Pedregal de San Ángel Reserve, Mexico",lab,both,both,25,25,NA,NA,25,25,25,25,250,250,family_mean_correlation,full_sib,no,broad,CC,non_adult,non_adult,development time from egg hatching to imago emergence,survival to sexual maturity,reverse_maturation,survival,include,cov,-0.170051594,"[-0.59, 0.15]",CI,0.91,"[0.44, 1.38]",CI,1.597,"[0.37, 3.6]",CI,control,table 2,maturation,survival,family,-0.171719793,25,-1,0.171719793,both,non_adult,Insecta,between
1402,Lema daturaphila,33,rayyan-697471303,Enhanced survival of a specialized leaf beetle reveals potential trade-offs with host utilization traits,2019,NA,"Pedregal de San Ángel Reserve, Mexico",lab,both,both,25,25,NA,NA,25,25,25,25,250,250,family_mean_correlation,full_sib,no,broad,CC,non_adult,adult,development time from egg hatching to imago emergence,adult mass at emergence,reverse_maturation,size,include,cov,0.197269264,"[-0.14, 0.44]",CI,0.91,"[0.44, 1.38]",CI,0.797,"[0.28, 1.33]",CI,control,table 2,maturation,size,family,0.199889647,25,-1,-0.199889647,both,cross,Insecta,between
1403,Lema daturaphila,33,rayyan-697471303,Enhanced survival of a specialized leaf beetle reveals potential trade-offs with host utilization traits,2019,NA,"Pedregal de San Ángel Reserve, Mexico",lab,both,both,25,25,NA,NA,25,25,25,25,250,250,family_mean_correlation,full_sib,yes,broad,CC,non_adult,adult,relative growth rate of larvae,adult mass at emergence,growth,size,include,cov,-0.453746303,"[-0.73, -0.01]",CI,0.88,"[0.46, 1.27]",CI,0.797,"[0.28, 1.33]",CI,selection,table 3,growth,size,family,-0.489407824,25,1,-0.489407824,both,cross,Insecta,between
1404,Leptinotarsa decemlineata,88,rayyan-697471730,The genetic architecture of a niche: Variation and covariation in host use traits in the Colorado potato beetle,2007,2005,"Brookhaven, Suffolk Co., New York, USA",lab,both,both,66,54,NA,NA,66,54,33,27,198,162,sire_mean_correlation,half_sib,no,narrow,authors,non_adult,adult,larval weight after 48 h ,adult weight (24 hr after eclosion),size,size,include_2,cor,0.18,NA,NA,NA,NA,NA,NA,NA,NA,Host_D_(SoCa)_blup,table s7,size,size,family,0.181982689,54,1,0.181982689,both,cross,Insecta,within
1406,Leptinotarsa decemlineata,88,rayyan-697471730,The genetic architecture of a niche: Variation and covariation in host use traits in the Colorado potato beetle,2007,2005,"Brookhaven, Suffolk Co., New York, USA",lab,both,both,66,54,NA,NA,66,54,33,27,198,162,sire_mean_correlation,half_sib,no,narrow,authors,non_adult,non_adult,larval weight after 48 h ,days to adult ,size,reverse_maturation,include_2,cor,-0.25,NA,NA,NA,NA,NA,NA,NA,NA,Host_D_(SoCa)_blup,table s7,size,maturation,family,-0.255412812,54,-1,0.255412812,both,non_adult,Insecta,between
1410,Leptinotarsa decemlineata,88,rayyan-697471730,The genetic architecture of a niche: Variation and covariation in host use traits in the Colorado potato beetle,2007,2005,"Brookhaven, Suffolk Co., New York, USA",lab,both,both,66,66,NA,NA,66,66,33,33,198,198,sire_mean_correlation,half_sib,no,narrow,authors,adult,non_adult,adult weight (24 hr after eclosion),days to adult ,size,reverse_maturation,include_2,cor,-0.26,NA,NA,NA,NA,NA,NA,NA,NA,Host_A_(SoTu)_blup,table s7,size,maturation,family,-0.266108407,66,-1,0.266108407,both,cross,Insecta,between
1412,Leptinotarsa decemlineata,88,rayyan-697471730,The genetic architecture of a niche: Variation and covariation in host use traits in the Colorado potato beetle,2007,2005,"Brookhaven, Suffolk Co., New York, USA",lab,both,both,66,66,NA,NA,66,66,33,33,198,198,sire_mean_correlation,half_sib,no,narrow,authors,non_adult,non_adult,larval weight after 48 h ,survival to adult,size,survival,include_2,cor,0.2,NA,NA,NA,NA,NA,NA,NA,NA,Host_D_(SoCa)_blup,table s7,size,survival,family,0.202732554,66,1,0.202732554,both,non_adult,Insecta,between
1417,Leptinotarsa decemlineata,88,rayyan-697471730,The genetic architecture of a niche: Variation and covariation in host use traits in the Colorado potato beetle,2007,2005,"Brookhaven, Suffolk Co., New York, USA",lab,both,both,54,54,NA,NA,54,54,27,27,162,162,sire_mean_correlation,half_sib,no,narrow,authors,adult,non_adult,adult weight (24 hr after eclosion),days to adult ,size,reverse_maturation,include_2,cor,-0.62,NA,NA,NA,NA,NA,NA,NA,NA,Host_D_(SoCa)_blup,table s7,size,maturation,family,-0.725005088,54,-1,0.725005088,both,cross,Insecta,between
1418,Leptinotarsa decemlineata,88,rayyan-697471730,The genetic architecture of a niche: Variation and covariation in host use traits in the Colorado potato beetle,2007,2005,"Brookhaven, Suffolk Co., New York, USA",lab,both,both,66,66,NA,NA,66,66,33,33,198,198,sire_mean_correlation,half_sib,no,narrow,authors,adult,non_adult,adult weight (24 hr after eclosion),survival to adult,size,survival,include_2,cor,0.16,NA,NA,NA,NA,NA,NA,NA,NA,Host_D_(SoCa)_blup,table s7,size,survival,family,0.161386696,66,1,0.161386696,both,cross,Insecta,between
1424,Leptinotarsa decemlineata,88,rayyan-697471730,The genetic architecture of a niche: Variation and covariation in host use traits in the Colorado potato beetle,2007,2005,"Brookhaven, Suffolk Co., New York, USA",lab,both,both,66,66,NA,NA,66,66,33,33,198,198,sire_mean_correlation,half_sib,no,narrow,authors,non_adult,adult,larval weight after 48 h ,adult weight (24 hr after eclosion),size,size,include_2,cor,0.11,NA,NA,NA,NA,NA,NA,NA,NA,Host_C_(SoDu)_blup,table s7,size,size,family,0.110446916,66,1,0.110446916,both,cross,Insecta,within
1426,Leptinotarsa decemlineata,88,rayyan-697471730,The genetic architecture of a niche: Variation and covariation in host use traits in the Colorado potato beetle,2007,2005,"Brookhaven, Suffolk Co., New York, USA",lab,both,both,66,66,NA,NA,66,66,33,33,198,198,sire_mean_correlation,half_sib,no,narrow,authors,adult,non_adult,adult weight (24 hr after eclosion),survival to adult,size,survival,include_2,cor,-0.0097,NA,NA,NA,NA,NA,NA,NA,NA,Host_A_(SoTu)_blup,table s7,size,survival,family,-0.009700304,66,1,-0.009700304,both,cross,Insecta,between
1427,Leptinotarsa decemlineata,88,rayyan-697471730,The genetic architecture of a niche: Variation and covariation in host use traits in the Colorado potato beetle,2007,2005,"Brookhaven, Suffolk Co., New York, USA",lab,both,both,66,66,NA,NA,66,66,33,33,198,198,sire_mean_correlation,half_sib,no,narrow,authors,non_adult,non_adult,days to adult,survival to adult,reverse_maturation,survival,include_2,cor,-0.026,NA,NA,NA,NA,NA,NA,NA,NA,Host_A_(SoTu)_blup,table s7,maturation,survival,family,-0.026005861,66,-1,0.026005861,both,non_adult,Insecta,between
1429,Leptinotarsa decemlineata,88,rayyan-697471730,The genetic architecture of a niche: Variation and covariation in host use traits in the Colorado potato beetle,2007,2005,"Brookhaven, Suffolk Co., New York, USA",lab,both,both,66,66,NA,NA,66,66,33,33,198,198,sire_mean_correlation,half_sib,no,narrow,authors,non_adult,non_adult,larval weight after 48 h ,days to adult ,size,reverse_maturation,include_2,cor,-0.089,NA,NA,NA,NA,NA,NA,NA,NA,Host_C_(SoDu)_blup,table s7,size,maturation,family,-0.089236113,66,-1,0.089236113,both,non_adult,Insecta,between
1430,Leptinotarsa decemlineata,88,rayyan-697471730,The genetic architecture of a niche: Variation and covariation in host use traits in the Colorado potato beetle,2007,2005,"Brookhaven, Suffolk Co., New York, USA",lab,both,both,66,66,NA,NA,66,66,33,33,198,198,sire_mean_correlation,half_sib,no,narrow,authors,adult,non_adult,adult weight (24 hr after eclosion),days to adult ,size,reverse_maturation,include_2,cor,-0.46,NA,NA,NA,NA,NA,NA,NA,NA,Host_C_(SoDu)_blup,table s7,size,maturation,family,-0.497311288,66,-1,0.497311288,both,cross,Insecta,between
1431,Leptinotarsa decemlineata,88,rayyan-697471730,The genetic architecture of a niche: Variation and covariation in host use traits in the Colorado potato beetle,2007,2005,"Brookhaven, Suffolk Co., New York, USA",lab,both,both,54,66,NA,NA,54,66,27,33,162,198,sire_mean_correlation,half_sib,no,narrow,authors,non_adult,non_adult,days to adult,survival to adult,reverse_maturation,survival,include_2,cor,0.21,NA,NA,NA,NA,NA,NA,NA,NA,Host_D_(SoCa)_blup,table s7,maturation,survival,family,0.213171347,54,-1,-0.213171347,both,non_adult,Insecta,between
1433,Leptinotarsa decemlineata,88,rayyan-697471730,The genetic architecture of a niche: Variation and covariation in host use traits in the Colorado potato beetle,2007,2005,"Brookhaven, Suffolk Co., New York, USA",lab,both,both,66,66,NA,NA,66,66,33,33,198,198,sire_mean_correlation,half_sib,no,narrow,authors,non_adult,non_adult,days to adult,survival to adult,reverse_maturation,survival,include_2,cor,0.057,NA,NA,NA,NA,NA,NA,NA,NA,Host_C_(SoDu)_blup,table s7,maturation,survival,family,0.057061852,66,-1,-0.057061852,both,non_adult,Insecta,between
1435,Leptinotarsa decemlineata,88,rayyan-697471730,The genetic architecture of a niche: Variation and covariation in host use traits in the Colorado potato beetle,2007,2005,"Brookhaven, Suffolk Co., New York, USA",lab,both,both,66,56,NA,NA,66,56,33,28,198,168,sire_mean_correlation,half_sib,no,narrow,authors,non_adult,adult,larval weight after 48 h ,adult weight (24 hr after eclosion),size,size,include_2,cor,-0.038,NA,NA,NA,NA,NA,NA,NA,NA,Host_B (SoRo) blup,table s7,size,size,family,-0.038018307,56,1,-0.038018307,both,cross,Insecta,within
1441,Leptinotarsa decemlineata,88,rayyan-697471730,The genetic architecture of a niche: Variation and covariation in host use traits in the Colorado potato beetle,2007,2005,"Brookhaven, Suffolk Co., New York, USA",lab,both,both,66,66,NA,NA,66,66,33,33,198,198,sire_mean_correlation,half_sib,no,narrow,authors,adult,non_adult,adult weight (24 hr after eclosion),survival to adult,size,survival,include_2,cor,0.15,NA,NA,NA,NA,NA,NA,NA,NA,Host_C_(SoDu)_blup,table s7,size,survival,family,0.151140436,66,1,0.151140436,both,cross,Insecta,between
1443,Leptinotarsa decemlineata,88,rayyan-697471730,The genetic architecture of a niche: Variation and covariation in host use traits in the Colorado potato beetle,2007,2005,"Brookhaven, Suffolk Co., New York, USA",lab,both,both,66,66,NA,NA,66,66,33,33,198,198,sire_mean_correlation,half_sib,no,narrow,authors,non_adult,non_adult,larval weight after 48 h ,survival to adult,size,survival,include_2,cor,-0.1,NA,NA,NA,NA,NA,NA,NA,NA,Host_C_(SoDu)_blup,table s7,size,survival,family,-0.100335348,66,1,-0.100335348,both,non_adult,Insecta,between
1444,Lestes sponsa,41,rayyan-697471328,The genetic variance but not the genetic covariance of life-history traits changes towards the north in a time-constrained insect,2018,2013,France,lab,both,both,54,54,NA,NA,54,54,NA,NA,540,540,animal_model,full_sib,no,broad,authors,non_adult,non_adult,larval development time (the number of days between hatching and emergence),growth rate (final instar larva head width/larval development time),reverse_maturation,growth,include,cor,-0.94,0.05,se,NA,NA,NA,NA,NA,NA,Southern,table 3,maturation,growth,family,-1.738049345,54,-1,1.738049345,both,non_adult,Insecta,between
1445,Lestes sponsa,41,rayyan-697471328,The genetic variance but not the genetic covariance of life-history traits changes towards the north in a time-constrained insect,2018,2013,Sweden,lab,both,both,44,44,NA,NA,44,44,NA,NA,440,440,animal_model,full_sib,no,broad,authors,non_adult,non_adult,egg development time (the number of days between date of initiation of spring and the date of hatching),growth rate (final instar larva head width/larval development time),reverse_maturation,growth,include,cor,0.94,0.19,se,NA,NA,NA,NA,NA,NA,Northern,table 3,maturation,growth,family,1.738049345,44,-1,-1.738049345,both,non_adult,Insecta,between
1446,Lestes sponsa,41,rayyan-697471328,The genetic variance but not the genetic covariance of life-history traits changes towards the north in a time-constrained insect,2018,2013,Poland,lab,both,both,39,39,NA,NA,39,39,NA,NA,390,390,animal_model,full_sib,no,broad,authors,non_adult,non_adult,egg development time (the number of days between date of initiation of spring and the date of hatching),growth rate (final instar larva head width/larval development time),reverse_maturation,growth,include,cor,0.9,0.08,se,NA,NA,NA,NA,NA,NA,Central,table 3,maturation,growth,family,1.47221949,39,-1,-1.47221949,both,non_adult,Insecta,between
1447,Lestes sponsa,41,rayyan-697471328,The genetic variance but not the genetic covariance of life-history traits changes towards the north in a time-constrained insect,2018,2013,Sweden,lab,both,both,44,44,NA,NA,44,44,NA,NA,440,440,animal_model,full_sib,no,broad,authors,non_adult,non_adult,larval development time (the number of days between hatching and emergence),growth rate (final instar larva head width/larval development time),reverse_maturation,growth,include,cor,-0.99,NA,NA,NA,NA,NA,NA,NA,NA,Northern,table 3,maturation,growth,family,-2.646652412,44,-1,2.646652412,both,non_adult,Insecta,between
1448,Lestes sponsa,41,rayyan-697471328,The genetic variance but not the genetic covariance of life-history traits changes towards the north in a time-constrained insect,2018,2013,France_poland_sweden,lab,both,both,24,24,NA,NA,24,24,NA,NA,144,144,animal_model,full_sib,no,broad,authors,non_adult,non_adult,egg development time (the number of days between date of initiation of spring and the date of hatching),growth rate (final instar larva head width/larval development time),reverse_maturation,growth,include,cor,0.25,0.39,se,NA,NA,NA,NA,NA,NA,common_garden,common garden vs. simulated conditions: question 2 ,maturation,growth,family,0.255412812,24,-1,-0.255412812,both,non_adult,Insecta,between
1449,Lestes sponsa,41,rayyan-697471328,The genetic variance but not the genetic covariance of life-history traits changes towards the north in a time-constrained insect,2018,2013,Poland,lab,both,both,39,39,NA,NA,39,39,NA,NA,390,390,animal_model,full_sib,no,broad,authors,non_adult,non_adult,larval development time (the number of days between hatching and emergence),growth rate (final instar larva head width/larval development time),reverse_maturation,growth,include,cor,-0.96,0.02,se,NA,NA,NA,NA,NA,NA,Central,table 3,maturation,growth,family,-1.945910149,39,-1,1.945910149,both,non_adult,Insecta,between
1450,Lestes sponsa,41,rayyan-697471328,The genetic variance but not the genetic covariance of life-history traits changes towards the north in a time-constrained insect,2018,2013,Sweden,lab,both,both,44,44,NA,NA,44,44,NA,NA,440,440,animal_model,full_sib,no,broad,authors,non_adult,non_adult,egg development time (the number of days between date of initiation of spring and the date of hatching),larval development time (the number of days between hatching and emergence),reverse_maturation,reverse_maturation,include,cor,-0.99,NA,NA,NA,NA,NA,NA,NA,NA,Northern,table 3,maturation,maturation,family,-2.646652412,44,1,-2.646652412,both,non_adult,Insecta,within
1451,Lestes sponsa,41,rayyan-697471328,The genetic variance but not the genetic covariance of life-history traits changes towards the north in a time-constrained insect,2018,2013,France_poland_sweden,lab,both,both,147,147,NA,NA,147,147,NA,NA,1470,1470,animal_model,full_sib,no,broad,authors,non_adult,non_adult,egg development time (the number of days between date of initiation of spring and the date of hatching),larval development time (the number of days between hatching and emergence),reverse_maturation,reverse_maturation,include,cor,-0.91,0.26,se,NA,NA,NA,NA,NA,NA,Southern_central_northern_combined,common garden vs. simulated conditions: question 2 ,maturation,maturation,family,-1.527524425,147,1,-1.527524425,both,non_adult,Insecta,within
1452,Lestes sponsa,41,rayyan-697471328,The genetic variance but not the genetic covariance of life-history traits changes towards the north in a time-constrained insect,2018,2013,France,lab,both,both,54,54,NA,NA,54,54,NA,NA,540,540,animal_model,full_sib,no,broad,authors,non_adult,non_adult,egg development time (the number of days between date of initiation of spring and the date of hatching),larval development time (the number of days between hatching and emergence),reverse_maturation,reverse_maturation,include,cor,-0.99,NA,NA,NA,NA,NA,NA,NA,NA,Southern,table 3,maturation,maturation,family,-2.646652412,54,1,-2.646652412,both,non_adult,Insecta,within
1453,Lestes sponsa,41,rayyan-697471328,The genetic variance but not the genetic covariance of life-history traits changes towards the north in a time-constrained insect,2018,2013,France,lab,both,both,54,54,NA,NA,54,54,NA,NA,540,540,animal_model,full_sib,no,broad,authors,non_adult,non_adult,egg development time (the number of days between date of initiation of spring and the date of hatching),growth rate (final instar larva head width/larval development time),reverse_maturation,growth,include,cor,0.88,0.13,se,NA,NA,NA,NA,NA,NA,Southern,table 3,maturation,growth,family,1.375767657,54,-1,-1.375767657,both,non_adult,Insecta,between
1454,Lestes sponsa,41,rayyan-697471328,The genetic variance but not the genetic covariance of life-history traits changes towards the north in a time-constrained insect,2018,2013,France_poland_sweden,lab,both,both,147,147,NA,NA,147,147,NA,NA,1470,1470,animal_model,full_sib,no,broad,authors,non_adult,non_adult,egg development time (the number of days between date of initiation of spring and the date of hatching),growth rate (final instar larva head width/larval development time),reverse_maturation,growth,include,cor,0.75,0.25,se,NA,NA,NA,NA,NA,NA,Southern_central_northern_combined,common garden vs. simulated conditions: question 2 ,maturation,growth,family,0.972955075,147,-1,-0.972955075,both,non_adult,Insecta,between
1455,Lestes sponsa,41,rayyan-697471328,The genetic variance but not the genetic covariance of life-history traits changes towards the north in a time-constrained insect,2018,2013,Poland,lab,both,both,39,39,NA,NA,39,39,NA,NA,390,390,animal_model,full_sib,no,broad,authors,non_adult,non_adult,egg development time (the number of days between date of initiation of spring and the date of hatching),larval development time (the number of days between hatching and emergence),reverse_maturation,reverse_maturation,include,cor,-0.9,0.09,se,NA,NA,NA,NA,NA,NA,Central,table 3,maturation,maturation,family,-1.47221949,39,1,-1.47221949,both,non_adult,Insecta,within
1456,Lestes sponsa,41,rayyan-697471328,The genetic variance but not the genetic covariance of life-history traits changes towards the north in a time-constrained insect,2018,2013,France_poland_sweden,lab,both,both,24,24,NA,NA,24,24,NA,NA,144,144,animal_model,full_sib,no,broad,authors,non_adult,non_adult,egg development time (the number of days between date of initiation of spring and the date of hatching),larval development time (the number of days between hatching and emergence),reverse_maturation,reverse_maturation,include,cor,0.5,0.27,se,NA,NA,NA,NA,NA,NA,common_garden,common garden vs. simulated conditions: question 2 ,maturation,maturation,family,0.549306144,24,1,0.549306144,both,non_adult,Insecta,within
1457,Lomaspilis marginata,63,rayyan-697471563,Latitudinal insect body size clines revisited: A critical evaluation of the saw-tooth model,2011,NA,Finland,lab,both,both,99,99,NA,NA,99,99,NA,NA,495,495,animal_model,half_sib,no,broad,authors,non_adult,non_adult,pupal mass,larval development time,size,reverse_maturation,include,cor,-0.384,"[-0.704, 0.179]",95CI,NA,NA,NA,NA,NA,NA,rayyan-697471563,table 2,size,maturation,family,-0.404743086,99,-1,0.404743086,both,non_adult,Insecta,between
1458,Lomaspilis marginata,63,rayyan-697471563,Latitudinal insect body size clines revisited: A critical evaluation of the saw-tooth model,2011,NA,Finland,lab,both,both,99,99,NA,NA,99,99,NA,NA,495,495,animal_model,half_sib,no,broad,authors,non_adult,non_adult,pupal mass,growth rate at the larval period ,size,growth,include,cor,0.586,"[0.0796, 0.826]",95CI,NA,NA,NA,NA,NA,NA,rayyan-697471563,table 2,size,growth,family,0.671552214,99,1,0.671552214,both,non_adult,Insecta,between
1459,Lomaspilis marginata,63,rayyan-697471563,Latitudinal insect body size clines revisited: A critical evaluation of the saw-tooth model,2011,NA,Finland,lab,both,both,99,99,NA,NA,99,99,NA,NA,495,495,animal_model,half_sib,no,broad,authors,non_adult,non_adult,larval development time,growth rate at the larval period ,reverse_maturation,growth,include,cor,-0.895,"[-0.950, 0.740]",95CI,NA,NA,NA,NA,NA,NA,rayyan-697471563,table 2,maturation,growth,family,-1.446506884,99,-1,1.446506884,both,non_adult,Insecta,between
1462,Lymantria dispar,83,rayyan-697471713,Genetic variation and correlations of life-history traits in gypsy moths (Lymantria dispar L.) from two populations in Serbia,2008,NA,"Ražanj, Serbia",lab,female,female,22,22,NA,NA,22,22,NA,NA,255,255,animal_model,full/half_sib,no,broad,authors,non_adult,non_adult,preadult development duration,pupal mass (second day of pupal development),reverse_maturation,size,include,cor,-0.863,NA,NA,NA,NA,NA,NA,NA,NA,Ražanj_female,table 3,maturation,size,family,-1.304981222,22,-1,1.304981222,female,non_adult,Insecta,between
1463,Lymantria dispar,83,rayyan-697471713,Genetic variation and correlations of life-history traits in gypsy moths (Lymantria dispar L.) from two populations in Serbia,2008,NA,"Ražanj, Serbia",lab,female,female,22,22,NA,NA,22,22,NA,NA,255,255,animal_model,full/half_sib,no,broad,authors,non_adult,non_adult,pupal duration,pupal mass (second day of pupal development),reverse_maturation,size,include,cor,-0.601,NA,NA,NA,NA,NA,NA,NA,NA,Ražanj_female,table 3,maturation,size,family,-0.694711148,22,-1,0.694711148,female,non_adult,Insecta,between
1464,Lymantria dispar,83,rayyan-697471713,Genetic variation and correlations of life-history traits in gypsy moths (Lymantria dispar L.) from two populations in Serbia,2008,NA,"Ražanj, Serbia",lab,male,male,22,22,NA,NA,22,22,NA,NA,263,263,animal_model,full/half_sib,no,broad,authors,non_adult,both,pupal mass (second day of pupal development),adult longevity,size,survival,include,cor,0.526,NA,NA,NA,NA,NA,NA,NA,NA,Ražanj_male,table 3,size,survival,family,0.584598945,22,1,0.584598945,male,cross,Insecta,between
1465,Lymantria dispar,83,rayyan-697471713,Genetic variation and correlations of life-history traits in gypsy moths (Lymantria dispar L.) from two populations in Serbia,2008,NA,"Ražanj, Serbia",lab,female,female,22,22,NA,NA,22,22,NA,NA,255,255,animal_model,full/half_sib,no,broad,authors,non_adult,non_adult,larval duration,pupal mass (second day of pupal development),reverse_maturation,size,include,cor,-0.858,NA,NA,NA,NA,NA,NA,NA,NA,Ražanj_female,table 3,maturation,size,family,-1.285714431,22,-1,1.285714431,female,non_adult,Insecta,between
1466,Lymantria dispar,83,rayyan-697471713,Genetic variation and correlations of life-history traits in gypsy moths (Lymantria dispar L.) from two populations in Serbia,2008,NA,"Ražanj, Serbia",lab,female,female,22,22,NA,NA,22,22,NA,NA,255,255,animal_model,full/half_sib,no,broad,authors,non_adult,both,pupal duration,adult longevity,reverse_maturation,survival,include,cor,-0.348,NA,NA,NA,NA,NA,NA,NA,NA,Ražanj_female,table 3,maturation,survival,family,-0.363166365,22,-1,0.363166365,female,cross,Insecta,between
1469,Lymantria dispar,83,rayyan-697471713,Genetic variation and correlations of life-history traits in gypsy moths (Lymantria dispar L.) from two populations in Serbia,2008,NA,"Ražanj, Serbia",lab,female,female,22,22,NA,NA,22,22,NA,NA,255,255,animal_model,full/half_sib,no,broad,authors,non_adult,both,preadult development duration,adult longevity,reverse_maturation,survival,include,cor,-0.75,NA,NA,NA,NA,NA,NA,NA,NA,Ražanj_female,table 3,maturation,survival,family,-0.972955075,22,-1,0.972955075,female,cross,Insecta,between
1470,Lymantria dispar,83,rayyan-697471713,Genetic variation and correlations of life-history traits in gypsy moths (Lymantria dispar L.) from two populations in Serbia,2008,NA,"Ražanj, Serbia",lab,female,female,22,22,NA,NA,22,22,NA,NA,255,255,animal_model,full/half_sib,no,broad,authors,non_adult,both,pupal mass (second day of pupal development),adult longevity,size,survival,include,cor,0.986,NA,NA,NA,NA,NA,NA,NA,NA,Ražanj_female,table 3,size,survival,family,2.477410257,22,1,2.477410257,female,cross,Insecta,between
1471,Lymantria dispar,83,rayyan-697471713,Genetic variation and correlations of life-history traits in gypsy moths (Lymantria dispar L.) from two populations in Serbia,2008,NA,"Despotovačke Šume, Serbia",lab,male,male,26,26,NA,NA,26,26,NA,NA,470,470,animal_model,full/half_sib,no,broad,authors,non_adult,non_adult,larval duration,pupal mass (second day of pupal development),reverse_maturation,size,include,cor,0.302,NA,NA,NA,NA,NA,NA,NA,NA,Despotovačke_Šume_male,table 3,maturation,size,family,0.31171886,26,-1,-0.31171886,male,non_adult,Insecta,between
1472,Lymantria dispar,83,rayyan-697471713,Genetic variation and correlations of life-history traits in gypsy moths (Lymantria dispar L.) from two populations in Serbia,2008,NA,"Despotovačke Šume, Serbia",lab,male,male,26,26,NA,NA,26,26,NA,NA,470,470,animal_model,full/half_sib,no,broad,authors,non_adult,both,larval duration,adult longevity,reverse_maturation,survival,include,cor,0.05,NA,NA,NA,NA,NA,NA,NA,NA,Despotovačke_Šume_male,table 3,maturation,survival,family,0.050041729,26,-1,-0.050041729,male,cross,Insecta,between
1473,Lymantria dispar,83,rayyan-697471713,Genetic variation and correlations of life-history traits in gypsy moths (Lymantria dispar L.) from two populations in Serbia,2008,NA,"Despotovačke Šume, Serbia",lab,male,male,26,26,NA,NA,26,26,NA,NA,470,470,animal_model,full/half_sib,no,broad,authors,non_adult,non_adult,pupal duration,preadult development duration,reverse_maturation,reverse_maturation,include,cor,0.873,NA,NA,NA,NA,NA,NA,NA,NA,Despotovačke_Šume_male,table 3,maturation,maturation,family,1.345554808,26,1,1.345554808,male,non_adult,Insecta,within
1474,Lymantria dispar,83,rayyan-697471713,Genetic variation and correlations of life-history traits in gypsy moths (Lymantria dispar L.) from two populations in Serbia,2008,NA,"Despotovačke Šume, Serbia",lab,male,male,26,26,NA,NA,26,26,NA,NA,470,470,animal_model,full/half_sib,no,broad,authors,non_adult,non_adult,larval duration,pupal duration,reverse_maturation,reverse_maturation,include,cor,0.789,NA,NA,NA,NA,NA,NA,NA,NA,Despotovačke_Šume_male,table 3,maturation,maturation,family,1.068776975,26,1,1.068776975,male,non_adult,Insecta,within
1477,Lymantria dispar,260,rayyan-197247446,Host plant effects on the genetic variation and correlations in the individual performance of the Gypsy Moth,1998,NA,"Sremac˘ki Rt, Serbia",lab,female,female,30,30,NA,NA,NA,NA,NA,NA,370,370,family_mean_correlation,full_sib,no,broad,authors,adult,non_adult,fecundity,the average mass of a fertilized egg,fertility,size,include,cor,-0.016,NA,NA,NA,NA,NA,NA,NA,NA,locust_female,table 4,fertility,size,family,-0.016001366,30,1,-0.016001366,female,cross,Insecta,between
1478,Lymantria dispar,334,rayyan-697472580,Effects of pathogen exposure on life-history variation in the gypsy moth (Lymantria dispar),2015,NA,"Michigan, Wisconsin, Indiana and Illinois,  US.",lab,both,both,NA,NA,NA,NA,125,125,23,23,769,769,animal_model,full_sib,no,narrow,authors,non_adult,non_adult,pupal weight,time to pupation,size,reverse_maturation,include,cor,-0.57,"[-0.77, -0.36]",95CI,NA,NA,NA,NA,NA,NA,rayyan-697472580,table 2,size,maturation,family,-0.647522845,125,-1,0.647522845,both,non_adult,Insecta,between
1483,Lymantria dispar,83,rayyan-697471713,Genetic variation and correlations of life-history traits in gypsy moths (Lymantria dispar L.) from two populations in Serbia,2008,NA,"Ražanj, Serbia",lab,male,male,22,22,NA,NA,22,22,NA,NA,263,263,animal_model,full/half_sib,no,broad,authors,non_adult,non_adult,pupal duration,pupal mass (second day of pupal development),reverse_maturation,size,include,cor,NA,NA,NA,NA,NA,NA,NA,NA,NA,Ražanj_male,table 3,maturation,size,family,NA,22,-1,NA,male,non_adult,Insecta,between
1484,Lymantria dispar,83,rayyan-697471713,Genetic variation and correlations of life-history traits in gypsy moths (Lymantria dispar L.) from two populations in Serbia,2008,NA,"Ražanj, Serbia",lab,male,male,22,22,NA,NA,22,22,NA,NA,263,263,animal_model,full/half_sib,no,broad,authors,non_adult,both,pupal duration,adult longevity,reverse_maturation,survival,include,cor,0.501,NA,NA,NA,NA,NA,NA,NA,NA,Ražanj_male,table 3,maturation,survival,family,0.550640368,22,-1,-0.550640368,male,cross,Insecta,between
1485,Lymantria dispar,83,rayyan-697471713,Genetic variation and correlations of life-history traits in gypsy moths (Lymantria dispar L.) from two populations in Serbia,2008,NA,"Ražanj, Serbia",lab,female,female,22,22,NA,NA,22,22,NA,NA,255,255,animal_model,full/half_sib,no,broad,authors,non_adult,non_adult,pupal duration,preadult development duration,reverse_maturation,reverse_maturation,include,cor,0.767,NA,NA,NA,NA,NA,NA,NA,NA,Ražanj_female,table 3,maturation,maturation,family,1.013000009,22,1,1.013000009,female,non_adult,Insecta,within
1486,Lymantria dispar,83,rayyan-697471713,Genetic variation and correlations of life-history traits in gypsy moths (Lymantria dispar L.) from two populations in Serbia,2008,NA,"Ražanj, Serbia",lab,male,male,22,22,NA,NA,22,22,NA,NA,263,263,animal_model,full/half_sib,no,broad,authors,non_adult,non_adult,preadult development duration,pupal mass (second day of pupal development),reverse_maturation,size,include,cor,-0.592,NA,NA,NA,NA,NA,NA,NA,NA,Ražanj_male,table 3,maturation,size,family,-0.680739596,22,-1,0.680739596,male,non_adult,Insecta,between
1487,Lymantria dispar,83,rayyan-697471713,Genetic variation and correlations of life-history traits in gypsy moths (Lymantria dispar L.) from two populations in Serbia,2008,NA,"Despotovačke Šume, Serbia",lab,male,male,26,26,NA,NA,26,26,NA,NA,470,470,animal_model,full/half_sib,no,broad,authors,non_adult,non_adult,pupal duration,pupal mass (second day of pupal development),reverse_maturation,size,include,cor,0.781,NA,NA,NA,NA,NA,NA,NA,NA,Despotovačke_Šume_male,table 3,maturation,size,family,1.047929277,26,-1,-1.047929277,male,non_adult,Insecta,between
1488,Lymantria dispar,260,rayyan-197247446,Host plant effects on the genetic variation and correlations in the individual performance of the Gypsy Moth,1998,NA,"Sremac˘ki Rt, Serbia",lab,female,female,30,30,NA,NA,NA,NA,NA,NA,383,370,family_mean_correlation,full_sib,no,broad,authors,both,non_adult,adult longevity,the average mass of a fertilized egg,survival,size,include,cor,0.156,NA,NA,NA,NA,NA,NA,NA,NA,locust_female,table 4,survival,size,family,0.157284277,30,1,0.157284277,female,cross,Insecta,between
1490,Lymantria dispar,260,rayyan-197247446,Host plant effects on the genetic variation and correlations in the individual performance of the Gypsy Moth,1998,NA,"Sremac˘ki Rt, Serbia",lab,female,female,30,30,NA,NA,NA,NA,NA,NA,383,370,family_mean_correlation,full_sib,no,broad,authors,non_adult,adult,1/development time from caterpillars hatching to adult emergence,fecundity,maturation,fertility,include,cor,0.153,NA,NA,NA,NA,NA,NA,NA,NA,locust_female,table 4,maturation,fertility,family,0.154210913,30,1,0.154210913,female,cross,Insecta,between
1492,Lymantria dispar,260,rayyan-197247446,Host plant effects on the genetic variation and correlations in the individual performance of the Gypsy Moth,1998,NA,"Sremac˘ki Rt, Serbia",lab,male,male,30,30,NA,NA,NA,NA,NA,NA,435,435,family_mean_correlation,full_sib,no,broad,authors,non_adult,non_adult,1/development time from caterpillars hatching to adult emergence,1/pupal development time,maturation,maturation,include,cor,0.609,NA,NA,NA,NA,NA,NA,NA,NA,oak_male,table 5,maturation,maturation,family,0.707330294,30,1,0.707330294,male,non_adult,Insecta,within
1493,Lymantria dispar,260,rayyan-197247446,Host plant effects on the genetic variation and correlations in the individual performance of the Gypsy Moth,1998,NA,"Sremac˘ki Rt, Serbia",lab,male,male,30,30,NA,NA,NA,NA,NA,NA,435,435,family_mean_correlation,full_sib,no,broad,authors,non_adult,non_adult,1/development time from caterpillars hatching to adult emergence,pupal mass on the second day of development,maturation,size,include,cor,-0.202,NA,NA,NA,NA,NA,NA,NA,NA,oak_male,table 5,maturation,size,family,-0.204816759,30,1,-0.204816759,male,non_adult,Insecta,between
1494,Lymantria dispar,260,rayyan-197247446,Host plant effects on the genetic variation and correlations in the individual performance of the Gypsy Moth,1998,NA,"Sremac˘ki Rt, Serbia",lab,male,male,30,30,NA,NA,NA,NA,NA,NA,435,435,family_mean_correlation,full_sib,no,broad,authors,non_adult,both,1/development time from caterpillars hatching to adult emergence,adult longevity,maturation,survival,include,cor,0.068,NA,NA,NA,NA,NA,NA,NA,NA,oak_male,table 5,maturation,survival,family,0.068105102,30,1,0.068105102,male,cross,Insecta,between
1495,Lymantria dispar,83,rayyan-697471713,Genetic variation and correlations of life-history traits in gypsy moths (Lymantria dispar L.) from two populations in Serbia,2008,NA,"Ražanj, Serbia",lab,female,female,22,22,NA,NA,22,22,NA,NA,255,255,animal_model,full/half_sib,no,broad,authors,non_adult,non_adult,larval duration,pupal duration,reverse_maturation,reverse_maturation,include,cor,0.732,NA,NA,NA,NA,NA,NA,NA,NA,Ražanj_female,table 3,maturation,maturation,family,0.933022554,22,1,0.933022554,female,non_adult,Insecta,within
1497,Lymantria dispar,260,rayyan-197247446,Host plant effects on the genetic variation and correlations in the individual performance of the Gypsy Moth,1998,NA,"Sremac˘ki Rt, Serbia",lab,female,female,30,30,NA,NA,NA,NA,NA,NA,383,383,family_mean_correlation,full_sib,no,broad,authors,non_adult,both,pupal mass on the second day of development,adult longevity,size,survival,include,cor,0.438,NA,NA,NA,NA,NA,NA,NA,NA,locust_female,table 4,size,survival,family,0.469753344,30,1,0.469753344,female,cross,Insecta,between
1498,Lymantria dispar,260,rayyan-197247446,Host plant effects on the genetic variation and correlations in the individual performance of the Gypsy Moth,1998,NA,"Sremac˘ki Rt, Serbia",lab,female,female,30,30,NA,NA,NA,NA,NA,NA,383,370,family_mean_correlation,full_sib,no,broad,authors,non_adult,adult,pupal mass on the second day of development,fecundity,size,fertility,include,cor,0.947,NA,NA,NA,NA,NA,NA,NA,NA,locust_female,table 4,size,fertility,family,1.801876546,30,1,1.801876546,female,cross,Insecta,between
1500,Lymantria dispar,83,rayyan-697471713,Genetic variation and correlations of life-history traits in gypsy moths (Lymantria dispar L.) from two populations in Serbia,2008,NA,"Ražanj, Serbia",lab,male,male,22,22,NA,NA,22,22,NA,NA,263,263,animal_model,full/half_sib,no,broad,authors,non_adult,both,preadult development duration,adult longevity,reverse_maturation,survival,include,cor,-0.719,NA,NA,NA,NA,NA,NA,NA,NA,Ražanj_male,table 3,maturation,survival,family,-0.905571668,22,-1,0.905571668,male,cross,Insecta,between
1502,Lymantria dispar,260,rayyan-197247446,Host plant effects on the genetic variation and correlations in the individual performance of the Gypsy Moth,1998,NA,"Sremac˘ki Rt, Serbia",lab,female,female,30,30,NA,NA,NA,NA,NA,NA,383,383,family_mean_correlation,full_sib,no,broad,authors,non_adult,both,1/development time from caterpillars hatching to adult emergence,adult longevity,maturation,survival,include,cor,0.471,NA,NA,NA,NA,NA,NA,NA,NA,locust_female,table 4,maturation,survival,family,0.511354644,30,1,0.511354644,female,cross,Insecta,between
1503,Lymantria dispar,83,rayyan-697471713,Genetic variation and correlations of life-history traits in gypsy moths (Lymantria dispar L.) from two populations in Serbia,2008,NA,"Despotovačke Šume, Serbia",lab,male,male,26,26,NA,NA,26,26,NA,NA,470,470,animal_model,full/half_sib,no,broad,authors,non_adult,non_adult,preadult development duration,pupal mass (second day of pupal development),reverse_maturation,size,include,cor,0.434,NA,NA,NA,NA,NA,NA,NA,NA,Despotovačke_Šume_male,table 3,maturation,size,family,0.464814471,26,-1,-0.464814471,male,non_adult,Insecta,between
1505,Lymantria dispar,260,rayyan-197247446,Host plant effects on the genetic variation and correlations in the individual performance of the Gypsy Moth,1998,NA,"Sremac˘ki Rt, Serbia",lab,female,female,30,30,NA,NA,NA,NA,NA,NA,383,370,family_mean_correlation,full_sib,no,broad,authors,non_adult,non_adult,1/development time from caterpillars hatching to adult emergence,the average mass of a fertilized egg,maturation,size,include,cor,0.409,NA,NA,NA,NA,NA,NA,NA,NA,locust_female,table 4,maturation,size,family,0.434409747,30,1,0.434409747,female,non_adult,Insecta,between
1506,Lymantria dispar,260,rayyan-197247446,Host plant effects on the genetic variation and correlations in the individual performance of the Gypsy Moth,1998,NA,"Sremac˘ki Rt, Serbia",lab,female,female,30,30,NA,NA,NA,NA,NA,NA,383,383,family_mean_correlation,full_sib,no,broad,authors,non_adult,non_adult,1/pupal development time,pupal mass on the second day of development,maturation,size,include,cor,-0.309,NA,NA,NA,NA,NA,NA,NA,NA,locust_female,table 4,maturation,size,family,-0.319439471,30,1,-0.319439471,female,non_adult,Insecta,between
1508,Lymantria dispar,83,rayyan-697471713,Genetic variation and correlations of life-history traits in gypsy moths (Lymantria dispar L.) from two populations in Serbia,2008,NA,"Ražanj, Serbia",lab,male,male,22,22,NA,NA,22,22,NA,NA,263,263,animal_model,full/half_sib,no,broad,authors,non_adult,non_adult,pupal duration,preadult development duration,reverse_maturation,reverse_maturation,include,cor,0.191,NA,NA,NA,NA,NA,NA,NA,NA,Ražanj_male,table 3,maturation,maturation,family,0.193374826,22,1,0.193374826,male,non_adult,Insecta,within
1509,Lymantria dispar,260,rayyan-197247446,Host plant effects on the genetic variation and correlations in the individual performance of the Gypsy Moth,1998,NA,"Sremac˘ki Rt, Serbia",lab,male,male,30,30,NA,NA,NA,NA,NA,NA,435,435,family_mean_correlation,full_sib,no,broad,authors,non_adult,non_adult,1/pupal development time,pupal mass on the second day of development,maturation,size,include,cor,-0.497,NA,NA,NA,NA,NA,NA,NA,NA,oak_male,table 5,maturation,size,family,-0.545314107,30,1,-0.545314107,male,non_adult,Insecta,between
1510,Lymantria dispar,260,rayyan-197247446,Host plant effects on the genetic variation and correlations in the individual performance of the Gypsy Moth,1998,NA,"Sremac˘ki Rt, Serbia",lab,male,male,30,30,NA,NA,NA,NA,NA,NA,435,435,family_mean_correlation,full_sib,no,broad,authors,non_adult,both,1/pupal development time,adult longevity,maturation,survival,include,cor,0.076,NA,NA,NA,NA,NA,NA,NA,NA,oak_male,table 5,maturation,survival,family,0.076146835,30,1,0.076146835,male,cross,Insecta,between
1511,Lymantria dispar,260,rayyan-197247446,Host plant effects on the genetic variation and correlations in the individual performance of the Gypsy Moth,1998,NA,"Sremac˘ki Rt, Serbia",lab,male,male,30,30,NA,NA,NA,NA,NA,NA,435,435,family_mean_correlation,full_sib,no,broad,authors,non_adult,both,pupal mass on the second day of development,adult longevity,size,survival,include,cor,0.139,NA,NA,NA,NA,NA,NA,NA,NA,oak_male,table 5,size,survival,family,0.13990573,30,1,0.13990573,male,cross,Insecta,between
1512,Lymantria dispar,260,rayyan-197247446,Host plant effects on the genetic variation and correlations in the individual performance of the Gypsy Moth,1998,NA,"Sremac˘ki Rt, Serbia",lab,male,male,30,30,NA,NA,NA,NA,NA,NA,434,434,family_mean_correlation,full_sib,no,broad,authors,non_adult,non_adult,1/development time from caterpillars hatching to adult emergence,1/pupal development time,maturation,maturation,include,cor,0.306,NA,NA,NA,NA,NA,NA,NA,NA,locust_male,tabe 5,maturation,maturation,family,0.316126175,30,1,0.316126175,male,non_adult,Insecta,within
1513,Lymantria dispar,260,rayyan-197247446,Host plant effects on the genetic variation and correlations in the individual performance of the Gypsy Moth,1998,NA,"Sremac˘ki Rt, Serbia",lab,female,female,30,30,NA,NA,NA,NA,NA,NA,383,370,family_mean_correlation,full_sib,no,broad,authors,non_adult,non_adult,pupal mass on the second day of development,the average mass of a fertilized egg,size,size,include,cor,0.144,NA,NA,NA,NA,NA,NA,NA,NA,locust_female,table 4,size,size,family,0.145007898,30,1,0.145007898,female,non_adult,Insecta,within
1514,Lymantria dispar,260,rayyan-197247446,Host plant effects on the genetic variation and correlations in the individual performance of the Gypsy Moth,1998,NA,"Sremac˘ki Rt, Serbia",lab,female,female,30,30,NA,NA,NA,NA,NA,NA,383,370,family_mean_correlation,full_sib,no,broad,authors,both,adult,adult longevity,fecundity,survival,fertility,include,cor,0.489,NA,NA,NA,NA,NA,NA,NA,NA,locust_female,table 4,survival,fertility,family,0.534745221,30,1,0.534745221,female,cross,Insecta,between
1515,Lymantria dispar,83,rayyan-697471713,Genetic variation and correlations of life-history traits in gypsy moths (Lymantria dispar L.) from two populations in Serbia,2008,NA,"Despotovačke Šume, Serbia",lab,male,male,26,26,NA,NA,26,26,NA,NA,470,470,animal_model,full/half_sib,no,broad,authors,non_adult,both,pupal duration,adult longevity,reverse_maturation,survival,include,cor,-0.156,NA,NA,NA,NA,NA,NA,NA,NA,Despotovačke_Šume_male,table 3,maturation,survival,family,-0.157284277,26,-1,0.157284277,male,cross,Insecta,between
1516,Lymantria dispar,260,rayyan-197247446,Host plant effects on the genetic variation and correlations in the individual performance of the Gypsy Moth,1998,NA,"Sremac˘ki Rt, Serbia",lab,male,male,30,30,NA,NA,NA,NA,NA,NA,434,434,family_mean_correlation,full_sib,no,broad,authors,non_adult,both,pupal mass on the second day of development,adult longevity,size,survival,include,cor,0.194,NA,NA,NA,NA,NA,NA,NA,NA,locust_male,tabe 5,size,survival,family,0.196490276,30,1,0.196490276,male,cross,Insecta,between
1517,Lymantria dispar,83,rayyan-697471713,Genetic variation and correlations of life-history traits in gypsy moths (Lymantria dispar L.) from two populations in Serbia,2008,NA,"Despotovačke Šume, Serbia",lab,male,male,26,26,NA,NA,26,26,NA,NA,470,470,animal_model,full/half_sib,no,broad,authors,non_adult,both,preadult development duration,adult longevity,reverse_maturation,survival,include,cor,0.001,NA,NA,NA,NA,NA,NA,NA,NA,Despotovačke_Šume_male,table 3,maturation,survival,family,0.001,26,-1,-0.001,male,cross,Insecta,between
1518,Lymantria dispar,83,rayyan-697471713,Genetic variation and correlations of life-history traits in gypsy moths (Lymantria dispar L.) from two populations in Serbia,2008,NA,"Despotovačke Šume, Serbia",lab,male,male,26,26,NA,NA,26,26,NA,NA,470,470,animal_model,full/half_sib,no,broad,authors,non_adult,both,pupal mass (second day of pupal development),adult longevity,size,survival,include,cor,0.264,NA,NA,NA,NA,NA,NA,NA,NA,Despotovačke_Šume_male,table 3,size,survival,family,0.270403228,26,1,0.270403228,male,cross,Insecta,between
1523,Lymantria dispar,83,rayyan-697471713,Genetic variation and correlations of life-history traits in gypsy moths (Lymantria dispar L.) from two populations in Serbia,2008,NA,"Ražanj, Serbia",lab,male,male,22,22,NA,NA,22,22,NA,NA,263,263,animal_model,full/half_sib,no,broad,authors,non_adult,both,larval duration,adult longevity,reverse_maturation,survival,include,cor,-0.772,NA,NA,NA,NA,NA,NA,NA,NA,Ražanj_male,table 3,maturation,survival,family,-1.025259251,22,-1,1.025259251,male,cross,Insecta,between
1525,Lymantria dispar,83,rayyan-697471713,Genetic variation and correlations of life-history traits in gypsy moths (Lymantria dispar L.) from two populations in Serbia,2008,NA,"Ražanj, Serbia",lab,female,female,22,22,NA,NA,22,22,NA,NA,255,255,animal_model,full/half_sib,no,broad,authors,non_adult,both,larval duration,adult longevity,reverse_maturation,survival,include,cor,-0.76,NA,NA,NA,NA,NA,NA,NA,NA,Ražanj_female,table 3,maturation,survival,family,-0.996215082,22,-1,0.996215082,female,cross,Insecta,between
1527,Lymantria dispar,260,rayyan-197247446,Host plant effects on the genetic variation and correlations in the individual performance of the Gypsy Moth,1998,NA,"Sremac˘ki Rt, Serbia",lab,female,female,30,30,NA,NA,NA,NA,NA,NA,383,383,family_mean_correlation,full_sib,no,broad,authors,non_adult,non_adult,1/development time from caterpillars hatching to adult emergence,1/pupal development time,maturation,maturation,include,cor,0.676,NA,NA,NA,NA,NA,NA,NA,NA,locust_female,table 4,maturation,maturation,family,0.821710883,30,1,0.821710883,female,non_adult,Insecta,within
1528,Lymantria dispar,260,rayyan-197247446,Host plant effects on the genetic variation and correlations in the individual performance of the Gypsy Moth,1998,NA,"Sremac˘ki Rt, Serbia",lab,female,female,30,30,NA,NA,NA,NA,NA,NA,383,383,family_mean_correlation,full_sib,no,broad,authors,non_adult,non_adult,1/development time from caterpillars hatching to adult emergence,pupal mass on the second day of development,maturation,size,include,cor,0.144,NA,NA,NA,NA,NA,NA,NA,NA,locust_female,table 4,maturation,size,family,0.145007898,30,1,0.145007898,female,non_adult,Insecta,between
1529,Lymantria dispar,289,rayyan-197247809,Pre-adult development and longevity in natural populations of Lymantria dispar (Lepidoptera : Lymantriidae),2007,1995,"Despotovacke šume, Serbia",lab,female,female,30,30,NA,NA,30,30,NA,NA,NA,NA,animal_model,full_sib,no,broad,authors,non_adult,both,development time,longevity,reverse_maturation,survival,include,cor,-0.254,0.283,se,NA,NA,NA,NA,NA,NA,Female_Quercus_Oak,table 2,maturation,survival,family,-0.25968406,30,-1,0.25968406,female,cross,Insecta,between
1530,Lymantria dispar,289,rayyan-197247809,Pre-adult development and longevity in natural populations of Lymantria dispar (Lepidoptera : Lymantriidae),2007,1995,"Despotovacke šume, Serbia",lab,female,female,30,30,NA,NA,30,30,NA,NA,NA,NA,animal_model,full_sib,no,broad,authors,non_adult,both,development time,longevity,reverse_maturation,survival,include,cor,-0.385,0.123,se,NA,NA,NA,NA,NA,NA,Female_Quercus_Locust,table 2,maturation,survival,family,-0.405916575,30,-1,0.405916575,female,cross,Insecta,between
1532,Lymantria dispar,289,rayyan-197247809,Pre-adult development and longevity in natural populations of Lymantria dispar (Lepidoptera : Lymantriidae),2007,1995,"Backa Palanka, Serbia",lab,female,female,35,35,NA,NA,35,35,NA,NA,NA,NA,animal_model,full_sib,no,broad,authors,non_adult,both,development time,longevity,reverse_maturation,survival,include,cor,-0.003,0.264,se,NA,NA,NA,NA,NA,NA,Female_Robinia_Locust,table 2,maturation,survival,family,-0.003000009,35,-1,0.003000009,female,cross,Insecta,between
1533,Lymantria dispar,289,rayyan-197247809,Pre-adult development and longevity in natural populations of Lymantria dispar (Lepidoptera : Lymantriidae),2007,1995,"Despotovacke šume, Serbia",lab,male,male,30,30,NA,NA,30,30,NA,NA,NA,NA,animal_model,full_sib,no,broad,authors,non_adult,both,development time,longevity,reverse_maturation,survival,include,cor,-0.369,0.201,se,NA,NA,NA,NA,NA,NA,male_Quercus_Oak,table 2,maturation,survival,family,-0.387264981,30,-1,0.387264981,male,cross,Insecta,between
1535,Lymantria dispar,260,rayyan-197247446,Host plant effects on the genetic variation and correlations in the individual performance of the Gypsy Moth,1998,NA,"Sremac˘ki Rt, Serbia",lab,female,female,30,30,NA,NA,NA,NA,NA,NA,383,370,family_mean_correlation,full_sib,no,broad,authors,non_adult,adult,1/pupal development time,fecundity,maturation,fertility,include,cor,-0.254,NA,NA,NA,NA,NA,NA,NA,NA,locust_female,table 4,maturation,fertility,family,-0.25968406,30,1,-0.25968406,female,cross,Insecta,between
1537,Lymantria dispar,260,rayyan-197247446,Host plant effects on the genetic variation and correlations in the individual performance of the Gypsy Moth,1998,NA,"Sremac˘ki Rt, Serbia",lab,female,female,30,30,NA,NA,NA,NA,NA,NA,383,370,family_mean_correlation,full_sib,no,broad,authors,non_adult,non_adult,1/pupal development time,the average mass of a fertilized egg,maturation,size,include,cor,0.214,NA,NA,NA,NA,NA,NA,NA,NA,locust_female,table 4,maturation,size,family,0.21735959,30,1,0.21735959,female,non_adult,Insecta,between
1542,Lymantria dispar,260,rayyan-197247446,Host plant effects on the genetic variation and correlations in the individual performance of the Gypsy Moth,1998,NA,"Sremac˘ki Rt, Serbia",lab,male,male,30,30,NA,NA,NA,NA,NA,NA,434,434,family_mean_correlation,full_sib,no,broad,authors,non_adult,non_adult,1/pupal development time,pupal mass on the second day of development,maturation,size,include,cor,-0.211,NA,NA,NA,NA,NA,NA,NA,NA,locust_male,tabe 5,maturation,size,family,-0.214217711,30,1,-0.214217711,male,non_adult,Insecta,between
1543,Lymantria dispar,260,rayyan-197247446,Host plant effects on the genetic variation and correlations in the individual performance of the Gypsy Moth,1998,NA,"Sremac˘ki Rt, Serbia",lab,male,male,30,30,NA,NA,NA,NA,NA,NA,434,434,family_mean_correlation,full_sib,no,broad,authors,non_adult,both,1/pupal development time,adult longevity,maturation,survival,include,cor,0.11,NA,NA,NA,NA,NA,NA,NA,NA,locust_male,tabe 5,maturation,survival,family,0.110446916,30,1,0.110446916,male,cross,Insecta,between
1544,Lymantria dispar,289,rayyan-197247809,Pre-adult development and longevity in natural populations of Lymantria dispar (Lepidoptera : Lymantriidae),2007,1995,"Backa Palanka, Serbia",lab,female,female,35,35,NA,NA,35,35,NA,NA,NA,NA,animal_model,full_sib,no,broad,authors,non_adult,both,development time,longevity,reverse_maturation,survival,include,cor,-0.019,0.164,se,NA,NA,NA,NA,NA,NA,Female_Robinia_Oak,table 2,maturation,survival,family,-0.019002287,35,-1,0.019002287,female,cross,Insecta,between
1545,Lymantria dispar,260,rayyan-197247446,Host plant effects on the genetic variation and correlations in the individual performance of the Gypsy Moth,1998,NA,"Sremac˘ki Rt, Serbia",lab,female,female,30,30,NA,NA,NA,NA,NA,NA,363,353,family_mean_correlation,full_sib,no,broad,authors,non_adult,adult,pupal mass on the second day of development,fecundity,size,fertility,include,cor,0.85,NA,NA,NA,NA,NA,NA,NA,NA,oak_female,table 4,size,fertility,family,1.256152812,30,1,1.256152812,female,cross,Insecta,between
1547,Lymantria dispar,260,rayyan-197247446,Host plant effects on the genetic variation and correlations in the individual performance of the Gypsy Moth,1998,NA,"Sremac˘ki Rt, Serbia",lab,female,female,30,30,NA,NA,NA,NA,NA,NA,383,383,family_mean_correlation,full_sib,no,broad,authors,non_adult,both,1/pupal development time,adult longevity,maturation,survival,include,cor,0.165,NA,NA,NA,NA,NA,NA,NA,NA,locust_female,table 4,maturation,survival,family,0.166522321,30,1,0.166522321,female,cross,Insecta,between
1548,Lymantria dispar,289,rayyan-197247809,Pre-adult development and longevity in natural populations of Lymantria dispar (Lepidoptera : Lymantriidae),2007,1995,"Backa Palanka, Serbia",lab,male,male,35,35,NA,NA,35,35,NA,NA,NA,NA,animal_model,full_sib,no,broad,authors,non_adult,both,development time,longevity,reverse_maturation,survival,include,cor,-0.912,0.041,se,NA,NA,NA,NA,NA,NA,male_Robinia_Oak,table 2,maturation,survival,family,-1.53928414,35,-1,1.53928414,male,cross,Insecta,between
1549,Lymantria dispar,289,rayyan-197247809,Pre-adult development and longevity in natural populations of Lymantria dispar (Lepidoptera : Lymantriidae),2007,1995,"Backa Palanka, Serbia",lab,male,male,35,35,NA,NA,35,35,NA,NA,NA,NA,animal_model,full_sib,no,broad,authors,non_adult,both,development time,longevity,reverse_maturation,survival,include,cor,NA,10.781,se,NA,NA,NA,NA,NA,NA,male_Robinia_Locust,table 2,maturation,survival,family,NA,35,-1,NA,male,cross,Insecta,between
1553,Lymantria dispar,260,rayyan-197247446,Host plant effects on the genetic variation and correlations in the individual performance of the Gypsy Moth,1998,NA,"Sremac˘ki Rt, Serbia",lab,male,male,30,30,NA,NA,NA,NA,NA,NA,434,434,family_mean_correlation,full_sib,no,broad,authors,non_adult,non_adult,1/development time from caterpillars hatching to adult emergence,pupal mass on the second day of development,maturation,size,include,cor,0.268,NA,NA,NA,NA,NA,NA,NA,NA,locust_male,tabe 5,maturation,size,family,0.274707811,30,1,0.274707811,male,non_adult,Insecta,between
1554,Lymantria dispar,260,rayyan-197247446,Host plant effects on the genetic variation and correlations in the individual performance of the Gypsy Moth,1998,NA,"Sremac˘ki Rt, Serbia",lab,male,male,30,30,NA,NA,NA,NA,NA,NA,434,434,family_mean_correlation,full_sib,no,broad,authors,non_adult,both,1/development time from caterpillars hatching to adult emergence,adult longevity,maturation,survival,include,cor,-0.348,NA,NA,NA,NA,NA,NA,NA,NA,locust_male,tabe 5,maturation,survival,family,-0.363166365,30,1,-0.363166365,male,cross,Insecta,between
1558,Lymantria dispar,83,rayyan-697471713,Genetic variation and correlations of life-history traits in gypsy moths (Lymantria dispar L.) from two populations in Serbia,2008,NA,"Despotovačke Šume, Serbia",lab,female,female,26,26,NA,NA,26,26,NA,NA,426,426,animal_model,full/half_sib,no,broad,authors,non_adult,non_adult,larval duration,pupal duration,reverse_maturation,reverse_maturation,include,cor,NA,NA,NA,NA,NA,NA,NA,NA,NA,Despotovačke_Šume_female,table 3,maturation,maturation,family,NA,26,1,NA,female,non_adult,Insecta,within
1559,Lymantria dispar,83,rayyan-697471713,Genetic variation and correlations of life-history traits in gypsy moths (Lymantria dispar L.) from two populations in Serbia,2008,NA,"Despotovačke Šume, Serbia",lab,female,female,26,26,NA,NA,26,26,NA,NA,426,426,animal_model,full/half_sib,no,broad,authors,non_adult,non_adult,larval duration,pupal mass (second day of pupal development),reverse_maturation,size,include,cor,0.659,NA,NA,NA,NA,NA,NA,NA,NA,Despotovačke_Šume_female,table 3,maturation,size,family,0.791043906,26,-1,-0.791043906,female,non_adult,Insecta,between
1560,Lymantria dispar,289,rayyan-197247809,Pre-adult development and longevity in natural populations of Lymantria dispar (Lepidoptera : Lymantriidae),2007,1995,"Despotovacke šume, Serbia",lab,male,male,30,30,NA,NA,30,30,NA,NA,NA,NA,animal_model,full_sib,no,broad,authors,non_adult,both,development time,longevity,reverse_maturation,survival,include,cor,-0.064,0.162,se,NA,NA,NA,NA,NA,NA,male_Quercus_Locust,table 2,maturation,survival,family,-0.064087597,30,-1,0.064087597,male,cross,Insecta,between
1563,Lymantria dispar,260,rayyan-197247446,Host plant effects on the genetic variation and correlations in the individual performance of the Gypsy Moth,1998,NA,"Sremac˘ki Rt, Serbia",lab,female,female,30,30,NA,NA,NA,NA,NA,NA,363,353,family_mean_correlation,full_sib,no,broad,authors,both,non_adult,adult longevity,the average mass of a fertilized egg,survival,size,include,cor,0.193,NA,NA,NA,NA,NA,NA,NA,NA,oak_female,table 4,survival,size,family,0.195451377,30,1,0.195451377,female,cross,Insecta,between
1564,Lymantria dispar,83,rayyan-697471713,Genetic variation and correlations of life-history traits in gypsy moths (Lymantria dispar L.) from two populations in Serbia,2008,NA,"Ražanj, Serbia",lab,male,male,22,22,NA,NA,22,22,NA,NA,263,263,animal_model,full/half_sib,no,broad,authors,non_adult,non_adult,larval duration,pupal mass (second day of pupal development),reverse_maturation,size,include,cor,-0.669,NA,NA,NA,NA,NA,NA,NA,NA,Ražanj_male,table 3,maturation,size,family,-0.808930774,22,-1,0.808930774,male,non_adult,Insecta,between
1565,Lymantria dispar,83,rayyan-697471713,Genetic variation and correlations of life-history traits in gypsy moths (Lymantria dispar L.) from two populations in Serbia,2008,NA,"Despotovačke Šume, Serbia",lab,female,female,26,26,NA,NA,26,26,NA,NA,426,426,animal_model,full/half_sib,no,broad,authors,non_adult,both,preadult development duration,adult longevity,reverse_maturation,survival,include,cor,-0.064,NA,NA,NA,NA,NA,NA,NA,NA,Despotovačke_Šume_female,table 3,maturation,survival,family,-0.064087597,26,-1,0.064087597,female,cross,Insecta,between
1566,Lymantria dispar,260,rayyan-197247446,Host plant effects on the genetic variation and correlations in the individual performance of the Gypsy Moth,1998,NA,"Sremac˘ki Rt, Serbia",lab,female,female,30,30,NA,NA,NA,NA,NA,NA,353,353,family_mean_correlation,full_sib,no,broad,authors,adult,non_adult,fecundity,the average mass of a fertilized egg,fertility,size,include,cor,-0.197,NA,NA,NA,NA,NA,NA,NA,NA,oak_female,table 4,fertility,size,family,-0.199609496,30,1,-0.199609496,female,cross,Insecta,between
1568,Lymantria dispar,260,rayyan-197247446,Host plant effects on the genetic variation and correlations in the individual performance of the Gypsy Moth,1998,NA,"Sremac˘ki Rt, Serbia",lab,female,female,30,30,NA,NA,NA,NA,NA,NA,363,363,family_mean_correlation,full_sib,no,broad,authors,non_adult,non_adult,1/pupal development time,pupal mass on the second day of development,maturation,size,include,cor,-0.199,NA,NA,NA,NA,NA,NA,NA,NA,oak_female,table 4,maturation,size,family,-0.201691104,30,1,-0.201691104,female,non_adult,Insecta,between
1569,Lymantria dispar,260,rayyan-197247446,Host plant effects on the genetic variation and correlations in the individual performance of the Gypsy Moth,1998,NA,"Sremac˘ki Rt, Serbia",lab,female,female,30,30,NA,NA,NA,NA,NA,NA,363,363,family_mean_correlation,full_sib,no,broad,authors,non_adult,both,1/pupal development time,adult longevity,maturation,survival,include,cor,-0.032,NA,NA,NA,NA,NA,NA,NA,NA,oak_female,table 4,maturation,survival,family,-0.032010929,30,1,-0.032010929,female,cross,Insecta,between
1571,Lymantria dispar,260,rayyan-197247446,Host plant effects on the genetic variation and correlations in the individual performance of the Gypsy Moth,1998,NA,"Sremac˘ki Rt, Serbia",lab,female,female,30,30,NA,NA,NA,NA,NA,NA,363,353,family_mean_correlation,full_sib,no,broad,authors,non_adult,non_adult,1/pupal development time,the average mass of a fertilized egg,maturation,size,include,cor,0.152,NA,NA,NA,NA,NA,NA,NA,NA,oak_female,table 4,maturation,size,family,0.153187103,30,1,0.153187103,female,non_adult,Insecta,between
1572,Lymantria dispar,260,rayyan-197247446,Host plant effects on the genetic variation and correlations in the individual performance of the Gypsy Moth,1998,NA,"Sremac˘ki Rt, Serbia",lab,female,female,30,30,NA,NA,NA,NA,NA,NA,363,363,family_mean_correlation,full_sib,no,broad,authors,non_adult,both,pupal mass on the second day of development,adult longevity,size,survival,include,cor,0.43,NA,NA,NA,NA,NA,NA,NA,NA,oak_female,table 4,size,survival,family,0.459896681,30,1,0.459896681,female,cross,Insecta,between
1573,Lymantria dispar,83,rayyan-697471713,Genetic variation and correlations of life-history traits in gypsy moths (Lymantria dispar L.) from two populations in Serbia,2008,NA,"Despotovačke Šume, Serbia",lab,female,female,26,26,NA,NA,26,26,NA,NA,426,426,animal_model,full/half_sib,no,broad,authors,non_adult,both,larval duration,adult longevity,reverse_maturation,survival,include,cor,-0.01,NA,NA,NA,NA,NA,NA,NA,NA,Despotovačke_Šume_female,table 3,maturation,survival,family,-0.010000333,26,-1,0.010000333,female,cross,Insecta,between
1574,Lymantria dispar,83,rayyan-697471713,Genetic variation and correlations of life-history traits in gypsy moths (Lymantria dispar L.) from two populations in Serbia,2008,NA,"Despotovačke Šume, Serbia",lab,female,female,26,26,NA,NA,26,26,NA,NA,426,426,animal_model,full/half_sib,no,broad,authors,non_adult,non_adult,pupal duration,preadult development duration,reverse_maturation,reverse_maturation,include,cor,NA,NA,NA,NA,NA,NA,NA,NA,NA,Despotovačke_Šume_female,table 3,maturation,maturation,family,NA,26,1,NA,female,non_adult,Insecta,within
1575,Lymantria dispar,83,rayyan-697471713,Genetic variation and correlations of life-history traits in gypsy moths (Lymantria dispar L.) from two populations in Serbia,2008,NA,"Despotovačke Šume, Serbia",lab,female,female,26,26,NA,NA,26,26,NA,NA,426,426,animal_model,full/half_sib,no,broad,authors,non_adult,non_adult,pupal duration,pupal mass (second day of pupal development),reverse_maturation,size,include,cor,0.502,NA,NA,NA,NA,NA,NA,NA,NA,Despotovačke_Šume_female,table 3,maturation,size,family,0.551976378,26,-1,-0.551976378,female,non_adult,Insecta,between
1576,Lymantria dispar,83,rayyan-697471713,Genetic variation and correlations of life-history traits in gypsy moths (Lymantria dispar L.) from two populations in Serbia,2008,NA,"Despotovačke Šume, Serbia",lab,female,female,26,26,NA,NA,26,26,NA,NA,426,426,animal_model,full/half_sib,no,broad,authors,non_adult,both,pupal duration,adult longevity,reverse_maturation,survival,include,cor,-0.564,NA,NA,NA,NA,NA,NA,NA,NA,Despotovačke_Šume_female,table 3,maturation,survival,family,-0.638679839,26,-1,0.638679839,female,cross,Insecta,between
1577,Lymantria dispar,83,rayyan-697471713,Genetic variation and correlations of life-history traits in gypsy moths (Lymantria dispar L.) from two populations in Serbia,2008,NA,"Despotovačke Šume, Serbia",lab,female,female,26,26,NA,NA,26,26,NA,NA,426,426,animal_model,full/half_sib,no,broad,authors,non_adult,non_adult,preadult development duration,pupal mass (second day of pupal development),reverse_maturation,size,include,cor,0.643,NA,NA,NA,NA,NA,NA,NA,NA,Despotovačke_Šume_female,table 3,maturation,size,family,0.763271668,26,-1,-0.763271668,female,non_adult,Insecta,between
1578,Lymantria dispar,260,rayyan-197247446,Host plant effects on the genetic variation and correlations in the individual performance of the Gypsy Moth,1998,NA,"Sremac˘ki Rt, Serbia",lab,female,female,30,30,NA,NA,NA,NA,NA,NA,363,353,family_mean_correlation,full_sib,no,broad,authors,non_adult,adult,1/development time from caterpillars hatching to adult emergence,fecundity,maturation,fertility,include,cor,0.103,NA,NA,NA,NA,NA,NA,NA,NA,oak_female,table 4,maturation,fertility,family,0.103366579,30,1,0.103366579,female,cross,Insecta,between
1579,Lymantria dispar,83,rayyan-697471713,Genetic variation and correlations of life-history traits in gypsy moths (Lymantria dispar L.) from two populations in Serbia,2008,NA,"Despotovačke Šume, Serbia",lab,female,female,26,26,NA,NA,26,26,NA,NA,426,426,animal_model,full/half_sib,no,broad,authors,non_adult,both,pupal mass (second day of pupal development),adult longevity,size,survival,include,cor,0.418,NA,NA,NA,NA,NA,NA,NA,NA,Despotovačke_Šume_female,table 3,size,survival,family,0.44526613,26,1,0.44526613,female,cross,Insecta,between
1580,Lymantria dispar,260,rayyan-197247446,Host plant effects on the genetic variation and correlations in the individual performance of the Gypsy Moth,1998,NA,"Sremac˘ki Rt, Serbia",lab,female,female,30,30,NA,NA,NA,NA,NA,NA,363,353,family_mean_correlation,full_sib,no,broad,authors,non_adult,non_adult,1/development time from caterpillars hatching to adult emergence,the average mass of a fertilized egg,maturation,size,include,cor,0.157,NA,NA,NA,NA,NA,NA,NA,NA,oak_female,table 4,maturation,size,family,0.158309385,30,1,0.158309385,female,non_adult,Insecta,between
1582,Lymantria dispar,83,rayyan-697471713,Genetic variation and correlations of life-history traits in gypsy moths (Lymantria dispar L.) from two populations in Serbia,2008,NA,"Ražanj, Serbia",lab,male,male,22,22,NA,NA,22,22,NA,NA,263,263,animal_model,full/half_sib,no,broad,authors,non_adult,non_adult,larval duration,pupal duration,reverse_maturation,reverse_maturation,include,cor,0.111,NA,NA,NA,NA,NA,NA,NA,NA,Ražanj_male,table 3,maturation,maturation,family,0.111459277,22,1,0.111459277,male,non_adult,Insecta,within
1583,Lymantria dispar,260,rayyan-197247446,Host plant effects on the genetic variation and correlations in the individual performance of the Gypsy Moth,1998,NA,"Sremac˘ki Rt, Serbia",lab,female,female,30,30,NA,NA,NA,NA,NA,NA,363,353,family_mean_correlation,full_sib,no,broad,authors,non_adult,adult,1/pupal development time,fecundity,maturation,fertility,include,cor,-0.071,NA,NA,NA,NA,NA,NA,NA,NA,oak_female,table 4,maturation,fertility,family,-0.071119666,30,1,-0.071119666,female,cross,Insecta,between
1587,Lymantria dispar,260,rayyan-197247446,Host plant effects on the genetic variation and correlations in the individual performance of the Gypsy Moth,1998,NA,"Sremac˘ki Rt, Serbia",lab,female,female,30,30,NA,NA,NA,NA,NA,NA,363,353,family_mean_correlation,full_sib,no,broad,authors,non_adult,non_adult,pupal mass on the second day of development,the average mass of a fertilized egg,size,size,include,cor,0.159,NA,NA,NA,NA,NA,NA,NA,NA,oak_female,table 4,size,size,family,0.160360592,30,1,0.160360592,female,non_adult,Insecta,within
1588,Lymantria dispar,260,rayyan-197247446,Host plant effects on the genetic variation and correlations in the individual performance of the Gypsy Moth,1998,NA,"Sremac˘ki Rt, Serbia",lab,female,female,30,30,NA,NA,NA,NA,NA,NA,363,353,family_mean_correlation,full_sib,no,broad,authors,both,adult,adult longevity,fecundity,survival,fertility,include,cor,0.278,NA,NA,NA,NA,NA,NA,NA,NA,oak_female,table 4,survival,fertility,family,0.285513248,30,1,0.285513248,female,cross,Insecta,between
1590,Lymantria dispar,260,rayyan-197247446,Host plant effects on the genetic variation and correlations in the individual performance of the Gypsy Moth,1998,NA,"Sremac˘ki Rt, Serbia",lab,female,female,30,30,NA,NA,NA,NA,NA,NA,363,363,family_mean_correlation,full_sib,no,broad,authors,non_adult,non_adult,1/development time from caterpillars hatching to adult emergence,pupal mass on the second day of development,maturation,size,include,cor,0.125,NA,NA,NA,NA,NA,NA,NA,NA,oak_female,table 4,maturation,size,family,0.125657214,30,1,0.125657214,female,non_adult,Insecta,between
1591,Lymantria dispar,260,rayyan-197247446,Host plant effects on the genetic variation and correlations in the individual performance of the Gypsy Moth,1998,NA,"Sremac˘ki Rt, Serbia",lab,female,female,30,30,NA,NA,NA,NA,NA,NA,363,363,family_mean_correlation,full_sib,no,broad,authors,non_adult,both,1/development time from caterpillars hatching to adult emergence,adult longevity,maturation,survival,include,cor,-0.168,NA,NA,NA,NA,NA,NA,NA,NA,oak_female,table 4,maturation,survival,family,-0.169607861,30,1,-0.169607861,female,cross,Insecta,between
1593,Lymantria dispar,260,rayyan-197247446,Host plant effects on the genetic variation and correlations in the individual performance of the Gypsy Moth,1998,NA,"Sremac˘ki Rt, Serbia",lab,female,female,30,30,NA,NA,NA,NA,NA,NA,363,363,family_mean_correlation,full_sib,no,broad,authors,non_adult,non_adult,1/development time from caterpillars hatching to adult emergence,1/pupal development time,maturation,maturation,include,cor,0.287,NA,NA,NA,NA,NA,NA,NA,NA,oak_female,table 4,maturation,maturation,family,0.295293894,30,1,0.295293894,female,non_adult,Insecta,within
1595,Lymnaea stagnalis,323,rayyan-697472525,Potential for adaptation to climate change: Family-level variation in fitness-related traits and their responses to heat waves in a snail population,2017,NA,,lab,both,both,15,15,NA,NA,15,15,NA,NA,600,600,animal_model,full_sib,no,broad,authors,adult,adult,shell length when matured,number of eggs,size,fertility,include,cor,0.925,0.048,se,NA,NA,NA,NA,NA,NA,25_c,table 2,size,fertility,family,1.622596567,15,1,1.622596567,both,adult,Gastropoda,between
1596,Lymnaea stagnalis,323,rayyan-697472525,Potential for adaptation to climate change: Family-level variation in fitness-related traits and their responses to heat waves in a snail population,2017,NA,"Zürich, Switzerland",lab,both,both,15,15,NA,NA,15,15,NA,NA,600,600,animal_model,full_sib,no,broad,authors,adult,adult,shell length when matured,number of eggs,size,fertility,include,cor,0.969,0.017,se,NA,NA,NA,NA,NA,NA,15_c,table 2,size,fertility,family,2.075646937,15,1,2.075646937,both,adult,Gastropoda,between
1598,Macaca mulatta,202,rayyan-197247251,Trade-off between age of first reproduction and survival in a female primate,2009,1960-2005,"Cayo Santiago, Puerto Rico",field,female,female,NA,NA,NA,NA,NA,NA,NA,NA,1067,286,animal_model,pedigree,no,narrow,authors,non_adult,both,age of first reproduction,adult survival rates to age 11,reverse_maturation,survival,include,cor,0.59,0.32,se,NA,NA,NA,NA,NA,NA,rayyan-197247251,table 1,maturation,survival,pedigree,0.677666068,286,-1,-0.677666068,female,cross,Mammalia,between
1599,Macaca mulatta,202,rayyan-197247251,Trade-off between age of first reproduction and survival in a female primate,2009,1960-2005,"Cayo Santiago, Puerto Rico",field,female,female,NA,NA,NA,NA,NA,NA,NA,NA,1067,264,animal_model,pedigree,no,narrow,authors,non_adult,both,age of first reproduction,adult survival rates to age 16,reverse_maturation,survival,include,cor,0.5945,0.215,se,NA,NA,NA,NA,NA,NA,rayyan-197247251,table 1,maturation,survival,pedigree,0.684597306,264,-1,-0.684597306,female,cross,Mammalia,between
1600,Macaca mulatta,202,rayyan-197247251,Trade-off between age of first reproduction and survival in a female primate,2009,1960-2005,"Cayo Santiago, Puerto Rico",field,female,female,NA,NA,NA,NA,NA,NA,NA,NA,1067,214,animal_model,pedigree,no,narrow,authors,non_adult,both,age of first reproduction,adult survival rates to age 21,reverse_maturation,survival,include,cor,0.4763,0.17,se,NA,NA,NA,NA,NA,NA,rayyan-197247251,table 1,maturation,survival,pedigree,0.518187618,214,-1,-0.518187618,female,cross,Mammalia,between
1604,Macaca mulatta,69,rayyan-697471637,Heritability of individual fitness in female macaques,2010,1959-1991,"Cayo Santiago, Puerto Rico",field,female,female,NA,NA,NA,NA,NA,NA,NA,NA,590,590,animal_model,pedigree,no,narrow,authors,adult,both,total number of offspring born to a female,lifespan,fertility,survival,include,cor,NA,0.008,se,NA,NA,NA,NA,NA,NA,uncensored,table 2,fertility,survival,pedigree,NA,590,1,NA,female,cross,Mammalia,between
1605,Macaca mulatta,202,rayyan-197247251,Trade-off between age of first reproduction and survival in a female primate,2009,1960-2005,"Cayo Santiago, Puerto Rico",field,female,female,NA,NA,NA,NA,NA,NA,NA,NA,1067,164,animal_model,pedigree,no,narrow,authors,non_adult,both,age of first reproduction,adult survival rates to age 26,reverse_maturation,survival,include,cor,0.7062,0.283,se,NA,NA,NA,NA,NA,NA,rayyan-197247251,table 1,maturation,survival,pedigree,0.879562345,164,-1,-0.879562345,female,cross,Mammalia,between
1607,Melospiza melodia,340,rayyan-697472625,Genetic covariance between components of male reproductive success: Within-pair vs. extra-pair paternity in song sparrows,2014,1993-2012,"Mandarte Island, BC, Canada",field,male,male,NA,NA,NA,NA,NA,NA,NA,NA,273,368,animal_model,pedigree,no,narrow,authors,adult,adult,within-pair paternity success ,extra-pair reproductive success,fertility,fertility,include,cor,0.56,"[0.01, 0.87]",95CI,NA,NA,NA,NA,NA,NA,rayyan-697472625,table 1,fertility,fertility,pedigree,0.632833187,273,1,0.632833187,male,adult,Aves,within
1608,Melospiza melodia,270,rayyan-197247535,Is there indirect selection on female extra-pair reproduction through cross-sex genetic correlations with male reproductive fitness?,2018,1993-2015,"Mandarte Island, BC, Canada",field,male,male,NA,NA,NA,NA,NA,NA,NA,NA,624,624,animal_model,pedigree,no,narrow,authors,adult,adult,male life time extra-pair reproductive success,male lifetime within-pair reproductive success,fertility,fertility,include,cor,0.79,"[0.57, 0.95]",95CI,NA,NA,NA,NA,NA,NA,rayyan-197247535,table 1,fertility,fertility,pedigree,1.071431684,624,1,1.071431684,male,adult,Aves,within
1611,Melospiza melodia,318,rayyan-697472464,Sex-specific additive genetic variances and correlations for fitness in a song sparrow (Melospiza melodia) population subject to natural immigration and inbreeding,2018,1994-2015,"British Columbia, Canada",field,both,female,NA,NA,NA,NA,NA,NA,NA,NA,585,526,animal_model,pedigree,no,narrow,authors,both,adult,adult survival,female annual reproductive success,survival,fertility,include,cor,0.072,"[-0.699, 0.846]",95CI,NA,NA,NA,NA,NA,NA,rayyan-697472464,figure s12,survival,fertility,pedigree,0.072124804,526,1,0.072124804,female,cross,Aves,between
1613,Melospiza melodia,318,rayyan-697472464,Sex-specific additive genetic variances and correlations for fitness in a song sparrow (Melospiza melodia) population subject to natural immigration and inbreeding,2018,1993-2014,"British Columbia, Canada",field,both,female,NA,NA,NA,NA,NA,NA,NA,NA,3104,243,animal_model,pedigree,no,narrow,authors,non_adult,adult,juvenile survival,female life time reproductive success,survival,fertility,include,cor,0.03,"[-0.73, 0.80]",95CI,NA,NA,NA,NA,NA,NA,rayyan-697472464,table 2,survival,fertility,pedigree,0.030009005,243,1,0.030009005,female,cross,Aves,between
1614,Melospiza melodia,318,rayyan-697472464,Sex-specific additive genetic variances and correlations for fitness in a song sparrow (Melospiza melodia) population subject to natural immigration and inbreeding,2018,1993-2014,"British Columbia, Canada",field,both,male,NA,NA,NA,NA,NA,NA,NA,NA,3104,312,animal_model,pedigree,no,narrow,authors,non_adult,adult,juvenile survival,male life time reproductive success,survival,fertility,include,cor,-0.08,"[-0.67, 0.58]",95CI,NA,NA,NA,NA,NA,NA,rayyan-697472464,table 2,survival,fertility,pedigree,-0.080171325,312,1,-0.080171325,male,cross,Aves,between
1615,Melospiza melodia,355,rayyan-697472773,Predicting evolutionary responses to selection on polyandry in the wild: Additive genetic covariances with female extra-pair reproduction,2012,1993-2009,"Mandarte Island, British Columbia, Canada",field,female,female,NA,NA,NA,NA,NA,NA,NA,NA,224,224,animal_model,pedigree,no,narrow,authors,adult,adult,relative annual reproductive success ,female liability to produce an extra-pair offspring,fertility,fertility,include,cov,0.628392296,"[-0.027, 0.199]",95CI,0.016,"[0.002, 0.039]",95CI,1.198,"[0.226, 271]",95CI,rayyan-697472773,table 2,fertility,fertility,pedigree,0.738754874,224,1,0.738754874,female,adult,Aves,within
1616,Melospiza melodia,318,rayyan-697472464,Sex-specific additive genetic variances and correlations for fitness in a song sparrow (Melospiza melodia) population subject to natural immigration and inbreeding,2018,1994-2015,"British Columbia, Canada",field,both,male,NA,NA,NA,NA,NA,NA,NA,NA,585,773,animal_model,pedigree,no,narrow,authors,both,adult,adult survival,male annual reproductive success,survival,fertility,include,cor,0.231,"[-0.55, 0.918]",95CI,NA,NA,NA,NA,NA,NA,rayyan-697472464,figure s12,survival,fertility,pedigree,0.235245578,585,1,0.235245578,male,cross,Aves,between
1617,Melospiza melodia,355,rayyan-697472773,Predicting evolutionary responses to selection on polyandry in the wild: Additive genetic covariances with female extra-pair reproduction,2012,1993-2009,"Mandarte Island, British Columbia, Canada",field,female,female,NA,NA,NA,NA,NA,NA,NA,NA,224,224,animal_model,pedigree,no,narrow,authors,non_adult,adult,relative offspring survived to recruit at age one on liability scale,relative annual reproductive success,survival,fertility,include,cov,0.323558522,"[-0.047, 0.090]",95CI,0.398,"[0.073, 0.796]",95CI,0.015,"[0.001, 0.038]",95CI,rayyan-697472773,table 2,survival,fertility,pedigree,0.335616651,224,1,0.335616651,female,cross,Aves,between
1619,Melospiza melodia,355,rayyan-697472773,Predicting evolutionary responses to selection on polyandry in the wild: Additive genetic covariances with female extra-pair reproduction,2012,1993-2009,"Mandarte Island, British Columbia, Canada",field,female,female,NA,NA,NA,NA,NA,NA,NA,NA,224,224,animal_model,pedigree,no,narrow,authors,non_adult,adult,relative offspring survived to recruit at age one on liability scale,female liability to produce an extra-pair offspring,survival,fertility,include,cov,0.227901499,"[-0.188, 0.522]",95CI,0.405,"[0.066, 0.768]",95CI,1.217,"[0.497, 2.093]",95CI,rayyan-697472773,table 2,survival,fertility,pedigree,0.23197488,224,1,0.23197488,female,cross,Aves,between
1620,Melospiza melodia,355,rayyan-697472773,Predicting evolutionary responses to selection on polyandry in the wild: Additive genetic covariances with female extra-pair reproduction,2012,1993-2009,"Mandarte Island, British Columbia, Canada",field,female,female,NA,NA,NA,NA,NA,NA,NA,NA,224,224,animal_model,pedigree,no,narrow,authors,non_adult,adult,relative offspring survived to recruit at age one on observed scale,female liability to produce an extra-pair offspring,survival,fertility,include,cov,0.236749313,"[-0.113, 0.320]",95CI,0.154,"[0.035, 0.278]",95CI,1.002,"[0.013, 1.810]",95CI,rayyan-697472773,table 2,survival,fertility,pedigree,0.241327581,224,1,0.241327581,female,cross,Aves,between
1621,Myodes glareolus,354,rayyan-697472769,Can number and size of offspring increase simultaneously? - A central life-history trade-off reconsidered,2012,2000,"Konnevesi, Finland",lab,female,both,NA,NA,35,35,NA,NA,NA,NA,2845,2845,animal_model,pedigree,yes,narrow,authors,adult,non_adult,litter size,birth mass,fertility,size,include,cor,0.54,0.23,se,NA,NA,NA,NA,NA,NA,rayyan-697472769,table 5,fertility,size,pedigree,0.604155603,2845,1,0.604155603,female,cross,Mammalia,between
1622,Myodes glareolus,177,rayyan-197247121,Quantitative genetics and fitness effects of basal metabolism,2013,NA,Finland,lab,female,female,NA,NA,NA,NA,NA,NA,NA,NA,161,876,animal_model,pedigree,no,narrow,authors,adult,adult,body mass,litter size,size,fertility,include,cor,0.19,0.45,se,NA,NA,NA,NA,NA,NA,rayyan-197247121,table 4,size,fertility,pedigree,0.192337169,161,1,0.192337169,female,adult,Mammalia,between
1623,Myodes glareolus,177,rayyan-197247121,Quantitative genetics and fitness effects of basal metabolism,2013,NA,Finland,lab,female,female,NA,NA,NA,NA,NA,NA,NA,NA,876,876,animal_model,pedigree,no,narrow,authors,adult,non_adult,litter size,offspring mass,fertility,size,include,cor,0.27,0.44,se,NA,NA,NA,NA,NA,NA,rayyan-197247121,table 4,fertility,size,pedigree,0.276863823,876,1,0.276863823,female,cross,Mammalia,between
1624,Myodes glareolus,177,rayyan-197247121,Quantitative genetics and fitness effects of basal metabolism,2013,NA,Finland,lab,female,female,NA,NA,NA,NA,NA,NA,NA,NA,161,876,animal_model,pedigree,no,narrow,authors,adult,non_adult,body mass,offspring mass,size,size,include,cor,0.64,0.59,se,NA,NA,NA,NA,NA,NA,rayyan-197247121,table 4,size,size,pedigree,0.758173745,161,1,0.758173745,female,cross,Mammalia,within
1625,Myodes glareolus,354,rayyan-697472769,Can number and size of offspring increase simultaneously? - A central life-history trade-off reconsidered,2012,2000,"Konnevesi, Finland",lab,female,both,NA,NA,35,35,NA,NA,NA,NA,2845,2845,animal_model,pedigree,yes,narrow,authors,adult,non_adult,litter size,birth head width,fertility,size,include,cor,0.47,0.26,se,NA,NA,NA,NA,NA,NA,rayyan-697472769,table 6,fertility,size,pedigree,0.510070337,2845,1,0.510070337,female,cross,Mammalia,between
1627,Myzus persicae,95,rayyan-697471766,Positive genetic correlations among major life-history traits related to ecological success in the aphid Myzus persicae,2005,2002-2003,"Melbourne,Australia",lab,female,female,NA,NA,19,19,608,608,NA,NA,608,608,animal_model,genetic_line,no,broad,authors,non_adult,adult,development time,daily fecundity 1 ,reverse_maturation,fertility,include,cor,-0.856,0.382,se,NA,NA,NA,NA,NA,NA,rg,table 2,maturation,fertility,genotype,-1.278182807,19,-1,1.278182807,female,cross,Insecta,between
1635,Myzus persicae,95,rayyan-697471766,Positive genetic correlations among major life-history traits related to ecological success in the aphid Myzus persicae,2005,2002-2003,"Melbourne,Australia",lab,female,female,NA,NA,19,19,608,608,NA,NA,608,608,animal_model,genetic_line,no,broad,authors,adult,adult,adult weight at ecdysis,daily fecundity 1 ,size,fertility,include,cor,NA,0.268,se,NA,NA,NA,NA,NA,NA,rg,table 2,size,fertility,genotype,NA,19,1,NA,female,adult,Insecta,between
1638,Myzus persicae,95,rayyan-697471766,Positive genetic correlations among major life-history traits related to ecological success in the aphid Myzus persicae,2005,2002-2003,"Melbourne,Australia",lab,female,female,NA,NA,19,19,608,608,NA,NA,608,608,animal_model,genetic_line,no,broad,authors,non_adult,adult,development time,adult weight at ecdysis,reverse_maturation,size,include,cor,-0.816,0.358,se,NA,NA,NA,NA,NA,NA,rg,table 2,maturation,size,genotype,-1.144727901,19,-1,1.144727901,female,cross,Insecta,between
1639,Myzus persicae,77,rayyan-697471690,Genetic variation and covariation of aphid life-history traits across unrelated host plants,2008,2003,"Melbourne, Autralia",lab,female,female,NA,NA,17,17,NA,NA,NA,NA,NA,NA,animal_model,genetic_line,no,broad,authors,adult,adult,adult weight (after ecdysis),"total offspring  (for the second five-day interval, reproduction at max rate)",size,fertility,include,cor,0.09,0.34,se,NA,NA,NA,NA,NA,NA,radish,table 2,size,fertility,genotype,0.090244188,17,1,0.090244188,female,adult,Insecta,between
1640,Myzus persicae,77,rayyan-697471690,Genetic variation and covariation of aphid life-history traits across unrelated host plants,2008,2003,"Melbourne, Autralia",lab,female,female,NA,NA,17,17,NA,NA,NA,NA,NA,NA,animal_model,genetic_line,no,broad,authors,adult,non_adult,adult weight (after ecdysis),offspring size (hind tibia length of newborn nymph),size,size,include,cor,0.98,0.18,se,NA,NA,NA,NA,NA,NA,radish,table 2,size,size,genotype,2.297559925,17,1,2.297559925,female,cross,Insecta,within
1641,Myzus persicae,95,rayyan-697471766,Positive genetic correlations among major life-history traits related to ecological success in the aphid Myzus persicae,2005,2002-2003,"Melbourne,Australia",lab,female,female,NA,NA,19,19,608,608,NA,NA,608,608,animal_model,genetic_line,no,broad,authors,adult,adult,adult weight at ecdysis,daily fecundity 3,size,fertility,include,cor,NA,0.437,se,NA,NA,NA,NA,NA,NA,rg,table 2,size,fertility,genotype,NA,19,1,NA,female,adult,Insecta,between
1644,Myzus persicae,77,rayyan-697471690,Genetic variation and covariation of aphid life-history traits across unrelated host plants,2008,2003,"Melbourne, Autralia",lab,female,female,NA,NA,17,17,NA,NA,NA,NA,NA,NA,animal_model,genetic_line,no,broad,authors,non_adult,adult,development time (time from birth to adult ecdysis),adult weight (after ecdysis),reverse_maturation,size,include,cor,-0.9,1.01,se,NA,NA,NA,NA,NA,NA,radish,table 2,maturation,size,genotype,-1.47221949,17,-1,1.47221949,female,cross,Insecta,between
1645,Myzus persicae,77,rayyan-697471690,Genetic variation and covariation of aphid life-history traits across unrelated host plants,2008,2003,"Melbourne, Autralia",lab,female,female,NA,NA,17,17,NA,NA,NA,NA,NA,NA,animal_model,genetic_line,no,broad,authors,non_adult,adult,development time (time from birth to adult ecdysis),"daily fecundity (for the second five-day interval, reproduction at max rate)",reverse_maturation,fertility,include,cor,-0.54,0.86,se,NA,NA,NA,NA,NA,NA,radish,table 2,maturation,fertility,genotype,-0.604155603,17,-1,0.604155603,female,cross,Insecta,between
1646,Myzus persicae,77,rayyan-697471690,Genetic variation and covariation of aphid life-history traits across unrelated host plants,2008,2003,"Melbourne, Autralia",lab,female,female,NA,NA,17,17,NA,NA,NA,NA,NA,NA,animal_model,genetic_line,no,broad,authors,non_adult,adult,development time (time from birth to adult ecdysis),"total offspring  (for the second five-day interval, reproduction at max rate)",reverse_maturation,fertility,include,cor,NA,1.24,se,NA,NA,NA,NA,NA,NA,radish,table 2,maturation,fertility,genotype,NA,17,-1,NA,female,cross,Insecta,between
1649,Myzus persicae,77,rayyan-697471690,Genetic variation and covariation of aphid life-history traits across unrelated host plants,2008,2003,"Melbourne, Autralia",lab,female,female,NA,NA,17,17,NA,NA,NA,NA,NA,NA,animal_model,genetic_line,no,broad,authors,non_adult,non_adult,development time (time from birth to adult ecdysis),offspring size (hind tibia length of newborn nymph),reverse_maturation,size,include,cor,-0.52,0.92,se,NA,NA,NA,NA,NA,NA,radish,table 2,maturation,size,genotype,-0.576339755,17,-1,0.576339755,female,non_adult,Insecta,between
1651,Myzus persicae,77,rayyan-697471690,Genetic variation and covariation of aphid life-history traits across unrelated host plants,2008,2003,"Melbourne, Autralia",lab,female,female,NA,NA,17,17,NA,NA,NA,NA,NA,NA,animal_model,genetic_line,no,broad,authors,adult,adult,adult weight (after ecdysis),"daily fecundity (for the second five-day interval, reproduction at max rate)",size,fertility,include,cor,0.28,0.35,se,NA,NA,NA,NA,NA,NA,radish,table 2,size,fertility,genotype,0.287682072,17,1,0.287682072,female,adult,Insecta,between
1653,Myzus persicae,77,rayyan-697471690,Genetic variation and covariation of aphid life-history traits across unrelated host plants,2008,2003,"Melbourne, Autralia",lab,female,female,NA,NA,17,17,NA,NA,NA,NA,NA,NA,animal_model,genetic_line,no,broad,authors,non_adult,non_adult,development time (time from birth to adult ecdysis),offspring size (hind tibia length of newborn nymph),reverse_maturation,size,include,cor,-0.51,0.47,se,NA,NA,NA,NA,NA,NA,lambsquarters,table 2,maturation,size,genotype,-0.562729769,17,-1,0.562729769,female,non_adult,Insecta,between
1657,Myzus persicae,95,rayyan-697471766,Positive genetic correlations among major life-history traits related to ecological success in the aphid Myzus persicae,2005,2002-2003,"Melbourne,Australia",lab,female,female,NA,NA,19,19,608,608,NA,NA,608,608,animal_model,genetic_line,no,broad,authors,non_adult,adult,development time,daily fecundity 4 ,reverse_maturation,fertility,include,cor,0.159,0.593,se,NA,NA,NA,NA,NA,NA,rg,table 2,maturation,fertility,genotype,0.160360592,19,-1,-0.160360592,female,cross,Insecta,between
1658,Myzus persicae,95,rayyan-697471766,Positive genetic correlations among major life-history traits related to ecological success in the aphid Myzus persicae,2005,2002-2003,"Melbourne,Australia",lab,female,female,NA,NA,19,19,608,608,NA,NA,608,608,animal_model,genetic_line,no,broad,authors,non_adult,adult,development time,total offspring ,reverse_maturation,fertility,include,cor,-0.739,0.232,se,NA,NA,NA,NA,NA,NA,rg,table 2,maturation,fertility,genotype,-0.948272554,19,-1,0.948272554,female,cross,Insecta,between
1659,Myzus persicae,95,rayyan-697471766,Positive genetic correlations among major life-history traits related to ecological success in the aphid Myzus persicae,2005,2002-2003,"Melbourne,Australia",lab,female,female,NA,NA,19,19,608,608,NA,NA,608,608,animal_model,genetic_line,no,broad,authors,non_adult,non_adult,development time,offspring size (hind tibia length of newborn first instar nymphs),reverse_maturation,size,include,cor,NA,0.52,se,NA,NA,NA,NA,NA,NA,rg,table 2,maturation,size,genotype,NA,19,-1,NA,female,non_adult,Insecta,between
1666,Myzus persicae,95,rayyan-697471766,Positive genetic correlations among major life-history traits related to ecological success in the aphid Myzus persicae,2005,2002-2003,"Melbourne,Australia",lab,female,female,NA,NA,19,19,608,608,NA,NA,608,608,animal_model,genetic_line,no,broad,authors,adult,adult,daily fecundity 2,daily fecundity 3,fertility,fertility,include,cor,0.769,0.205,se,NA,NA,NA,NA,NA,NA,rg,table 2,fertility,fertility,genotype,1.017875992,19,1,1.017875992,female,adult,Insecta,within
1667,Myzus persicae,95,rayyan-697471766,Positive genetic correlations among major life-history traits related to ecological success in the aphid Myzus persicae,2005,2002-2003,"Melbourne,Australia",lab,female,female,NA,NA,19,19,608,608,NA,NA,608,608,animal_model,genetic_line,no,broad,authors,adult,adult,adult weight at ecdysis,daily fecundity 4 ,size,fertility,include,cor,0.251,0.501,se,NA,NA,NA,NA,NA,NA,rg,table 2,size,fertility,genotype,0.256479763,19,1,0.256479763,female,adult,Insecta,between
1668,Myzus persicae,95,rayyan-697471766,Positive genetic correlations among major life-history traits related to ecological success in the aphid Myzus persicae,2005,2002-2003,"Melbourne,Australia",lab,female,female,NA,NA,19,19,608,608,NA,NA,608,608,animal_model,genetic_line,no,broad,authors,adult,adult,adult weight at ecdysis,total offspring ,size,fertility,include,cor,NA,0.472,se,NA,NA,NA,NA,NA,NA,rg,table 2,size,fertility,genotype,NA,19,1,NA,female,adult,Insecta,between
1669,Myzus persicae,95,rayyan-697471766,Positive genetic correlations among major life-history traits related to ecological success in the aphid Myzus persicae,2005,2002-2003,"Melbourne,Australia",lab,female,female,NA,NA,19,19,608,608,NA,NA,608,608,animal_model,genetic_line,no,broad,authors,non_adult,adult,development time,daily fecundity 2,reverse_maturation,fertility,include,cor,-0.688,0.488,se,NA,NA,NA,NA,NA,NA,rg,table 2,maturation,fertility,genotype,-0.844148244,19,-1,0.844148244,female,cross,Insecta,between
1670,Myzus persicae,95,rayyan-697471766,Positive genetic correlations among major life-history traits related to ecological success in the aphid Myzus persicae,2005,2002-2003,"Melbourne,Australia",lab,female,female,NA,NA,19,19,608,608,NA,NA,608,608,animal_model,genetic_line,no,broad,authors,non_adult,adult,development time,daily fecundity 3,reverse_maturation,fertility,include,cor,-0.661,0.699,se,NA,NA,NA,NA,NA,NA,rg,table 2,maturation,fertility,genotype,-0.794587501,19,-1,0.794587501,female,cross,Insecta,between
1677,Myzus persicae,77,rayyan-697471690,Genetic variation and covariation of aphid life-history traits across unrelated host plants,2008,2003,"Melbourne, Autralia",lab,female,female,NA,NA,17,17,NA,NA,NA,NA,NA,NA,animal_model,genetic_line,no,broad,authors,non_adult,adult,development time (time from birth to adult ecdysis),adult weight (after ecdysis),reverse_maturation,size,include,cor,-0.21,0.8,se,NA,NA,NA,NA,NA,NA,lambsquarters,table 2,maturation,size,genotype,-0.213171347,17,-1,0.213171347,female,cross,Insecta,between
1678,Myzus persicae,95,rayyan-697471766,Positive genetic correlations among major life-history traits related to ecological success in the aphid Myzus persicae,2005,2002-2003,"Melbourne,Australia",lab,female,female,NA,NA,19,19,608,608,NA,NA,608,608,animal_model,genetic_line,no,broad,authors,adult,adult,adult weight at ecdysis,daily fecundity 2,size,fertility,include,cor,0.972,0.324,se,NA,NA,NA,NA,NA,NA,rg,table 2,size,fertility,genotype,2.127299512,19,1,2.127299512,female,adult,Insecta,between
1680,Myzus persicae,95,rayyan-697471766,Positive genetic correlations among major life-history traits related to ecological success in the aphid Myzus persicae,2005,2002-2003,"Melbourne,Australia",lab,female,female,NA,NA,19,19,608,608,NA,NA,608,608,animal_model,genetic_line,no,broad,authors,adult,adult,daily fecundity 3,daily fecundity 4 ,fertility,fertility,include,cor,0.051,0.374,se,NA,NA,NA,NA,NA,NA,rg,table 2,fertility,fertility,genotype,0.051044286,19,1,0.051044286,female,adult,Insecta,within
1681,Myzus persicae,77,rayyan-697471690,Genetic variation and covariation of aphid life-history traits across unrelated host plants,2008,2003,"Melbourne, Autralia",lab,female,female,NA,NA,17,17,NA,NA,NA,NA,NA,NA,animal_model,genetic_line,no,broad,authors,non_adult,non_adult,development time (time from birth to adult ecdysis),offspring size (hind tibia length of newborn nymph),reverse_maturation,size,include,cor,-0.73,0.46,se,NA,NA,NA,NA,NA,NA,lambsquarters,table 2,maturation,size,genotype,-0.928727364,17,-1,0.928727364,female,non_adult,Insecta,between
1682,Myzus persicae,77,rayyan-697471690,Genetic variation and covariation of aphid life-history traits across unrelated host plants,2008,2003,"Melbourne, Autralia",lab,female,female,NA,NA,17,17,NA,NA,NA,NA,NA,NA,animal_model,genetic_line,no,broad,authors,adult,adult,"daily fecundity (for the second five-day interval, reproduction at max rate)","total offspring  (for the second five-day interval, reproduction at max rate)",fertility,fertility,include,cor,0.87,0.09,se,NA,NA,NA,NA,NA,NA,radish,table 2,fertility,fertility,genotype,1.33307963,17,1,1.33307963,female,adult,Insecta,within
1689,Myzus persicae,77,rayyan-697471690,Genetic variation and covariation of aphid life-history traits across unrelated host plants,2008,2003,"Melbourne, Autralia",lab,female,female,NA,NA,17,17,NA,NA,NA,NA,NA,NA,animal_model,genetic_line,no,broad,authors,adult,non_adult,"total offspring  (for the second five-day interval, reproduction at max rate)",offspring size (hind tibia length of newborn nymph),fertility,size,include,cor,0.85,0.43,se,NA,NA,NA,NA,NA,NA,lambsquarters,table 2,fertility,size,genotype,1.256152812,17,1,1.256152812,female,cross,Insecta,between
1693,Myzus persicae,77,rayyan-697471690,Genetic variation and covariation of aphid life-history traits across unrelated host plants,2008,2003,"Melbourne, Autralia",lab,female,female,NA,NA,17,17,NA,NA,NA,NA,NA,NA,animal_model,genetic_line,no,broad,authors,adult,non_adult,"daily fecundity (for the second five-day interval, reproduction at max rate)",offspring size (hind tibia length of newborn nymph),fertility,size,include,cor,0.55,0.26,se,NA,NA,NA,NA,NA,NA,radish,table 2,fertility,size,genotype,0.618381314,17,1,0.618381314,female,cross,Insecta,between
1694,Myzus persicae,77,rayyan-697471690,Genetic variation and covariation of aphid life-history traits across unrelated host plants,2008,2003,"Melbourne, Autralia",lab,female,female,NA,NA,17,17,NA,NA,NA,NA,NA,NA,animal_model,genetic_line,no,broad,authors,non_adult,adult,development time (time from birth to adult ecdysis),"daily fecundity (for the second five-day interval, reproduction at max rate)",reverse_maturation,fertility,include,cor,-0.21,0.75,se,NA,NA,NA,NA,NA,NA,lambsquarters,table 2,maturation,fertility,genotype,-0.213171347,17,-1,0.213171347,female,cross,Insecta,between
1697,Myzus persicae,77,rayyan-697471690,Genetic variation and covariation of aphid life-history traits across unrelated host plants,2008,2003,"Melbourne, Autralia",lab,female,female,NA,NA,17,17,NA,NA,NA,NA,NA,NA,animal_model,genetic_line,no,broad,authors,adult,non_adult,"total offspring  (for the second five-day interval, reproduction at max rate)",offspring size (hind tibia length of newborn nymph),fertility,size,include,cor,0.44,0.28,se,NA,NA,NA,NA,NA,NA,radish,table 2,fertility,size,genotype,0.472230804,17,1,0.472230804,female,cross,Insecta,between
1699,Myzus persicae,95,rayyan-697471766,Positive genetic correlations among major life-history traits related to ecological success in the aphid Myzus persicae,2005,2002-2003,"Melbourne,Australia",lab,female,female,NA,NA,19,19,608,608,NA,NA,608,608,animal_model,genetic_line,no,broad,authors,adult,adult,daily fecundity 2,daily fecundity 3,fertility,fertility,include,cor,0.607,0.488,se,NA,NA,NA,NA,NA,NA,rg,table 2,fertility,fertility,genotype,0.704157377,19,1,0.704157377,female,adult,Insecta,within
1701,Myzus persicae,95,rayyan-697471766,Positive genetic correlations among major life-history traits related to ecological success in the aphid Myzus persicae,2005,2002-2003,"Melbourne,Australia",lab,female,female,NA,NA,19,19,608,608,NA,NA,608,608,animal_model,genetic_line,no,broad,authors,adult,non_adult,adult weight at ecdysis,offspring size (hind tibia length of newborn first instar nymphs),size,size,include,cor,NA,0.686,se,NA,NA,NA,NA,NA,NA,rg,table 2,size,size,genotype,NA,19,1,NA,female,cross,Insecta,within
1702,Myzus persicae,95,rayyan-697471766,Positive genetic correlations among major life-history traits related to ecological success in the aphid Myzus persicae,2005,2002-2003,"Melbourne,Australia",lab,female,female,NA,NA,19,19,608,608,NA,NA,608,608,animal_model,genetic_line,no,broad,authors,adult,adult,daily fecundity 4,total offspring ,fertility,fertility,include,cor,0.655,0.364,se,NA,NA,NA,NA,NA,NA,rg,table 2,fertility,fertility,genotype,0.784005935,19,1,0.784005935,female,adult,Insecta,within
1703,Myzus persicae,95,rayyan-697471766,Positive genetic correlations among major life-history traits related to ecological success in the aphid Myzus persicae,2005,2002-2003,"Melbourne,Australia",lab,female,female,NA,NA,19,19,608,608,NA,NA,608,608,animal_model,genetic_line,no,broad,authors,adult,non_adult,daily fecundity 5,offspring size (hind tibia length of newborn first instar nymphs),fertility,size,include,cor,0.625,0.394,se,NA,NA,NA,NA,NA,NA,rg,table 2,fertility,size,genotype,0.733168534,19,1,0.733168534,female,cross,Insecta,between
1704,Myzus persicae,95,rayyan-697471766,Positive genetic correlations among major life-history traits related to ecological success in the aphid Myzus persicae,2005,2002-2003,"Melbourne,Australia",lab,female,female,NA,NA,19,19,608,608,NA,NA,608,608,animal_model,genetic_line,no,broad,authors,adult,adult,daily fecundity 4,total offspring ,fertility,fertility,include,cor,0.872,0.104,se,NA,NA,NA,NA,NA,NA,rg,table 2,fertility,fertility,genotype,1.341366197,19,1,1.341366197,female,adult,Insecta,within
1706,Myzus persicae,77,rayyan-697471690,Genetic variation and covariation of aphid life-history traits across unrelated host plants,2008,2003,"Melbourne, Autralia",lab,female,female,NA,NA,17,17,NA,NA,NA,NA,NA,NA,animal_model,genetic_line,no,broad,authors,adult,adult,adult weight (after ecdysis),"daily fecundity (for the second five-day interval, reproduction at max rate)",size,fertility,include,cor,-0.47,1.67,se,NA,NA,NA,NA,NA,NA,lambsquarters,table 2,size,fertility,genotype,-0.510070337,17,1,-0.510070337,female,adult,Insecta,between
1708,Myzus persicae,77,rayyan-697471690,Genetic variation and covariation of aphid life-history traits across unrelated host plants,2008,2003,"Melbourne, Autralia",lab,female,female,NA,NA,17,17,NA,NA,NA,NA,NA,NA,animal_model,genetic_line,no,broad,authors,adult,non_adult,adult weight (after ecdysis),offspring size (hind tibia length of newborn nymph),size,size,include,cor,0.34,0.81,se,NA,NA,NA,NA,NA,NA,lambsquarters,table 2,size,size,genotype,0.354092529,17,1,0.354092529,female,cross,Insecta,within
1710,Myzus persicae,77,rayyan-697471690,Genetic variation and covariation of aphid life-history traits across unrelated host plants,2008,2003,"Melbourne, Autralia",lab,female,female,NA,NA,17,17,NA,NA,NA,NA,NA,NA,animal_model,genetic_line,no,broad,authors,adult,non_adult,"daily fecundity (for the second five-day interval, reproduction at max rate)",offspring size (hind tibia length of newborn nymph),fertility,size,include,cor,0.66,0.52,se,NA,NA,NA,NA,NA,NA,lambsquarters,table 2,fertility,size,genotype,0.792813632,17,1,0.792813632,female,cross,Insecta,between
1711,Myzus persicae,77,rayyan-697471690,Genetic variation and covariation of aphid life-history traits across unrelated host plants,2008,2003,"Melbourne, Autralia",lab,female,female,NA,NA,17,17,NA,NA,NA,NA,NA,NA,animal_model,genetic_line,no,broad,authors,adult,adult,adult weight (after ecdysis),"total offspring  (for the second five-day interval, reproduction at max rate)",size,fertility,include,cor,NA,0.91,se,NA,NA,NA,NA,NA,NA,lambsquarters,table 2,size,fertility,genotype,NA,17,1,NA,female,adult,Insecta,between
1712,Myzus persicae,95,rayyan-697471766,Positive genetic correlations among major life-history traits related to ecological success in the aphid Myzus persicae,2005,2002-2003,"Melbourne,Australia",lab,female,female,NA,NA,19,19,608,608,NA,NA,608,608,animal_model,genetic_line,no,broad,authors,adult,non_adult,total offspring ,offspring size (hind tibia length of newborn first instar nymphs),fertility,size,include,cor,0.805,0.213,se,NA,NA,NA,NA,NA,NA,rg,table 2,fertility,size,genotype,1.112658156,19,1,1.112658156,female,cross,Insecta,between
1713,Myzus persicae,95,rayyan-697471766,Positive genetic correlations among major life-history traits related to ecological success in the aphid Myzus persicae,2005,2002-2003,"Melbourne,Australia",lab,female,female,NA,NA,19,19,608,608,NA,NA,608,608,animal_model,genetic_line,no,broad,authors,adult,adult,daily fecundity 1 ,daily fecundity 2,fertility,fertility,include,cor,0.673,0.423,se,NA,NA,NA,NA,NA,NA,rg,table 2,fertility,fertility,genotype,0.816206765,19,1,0.816206765,female,adult,Insecta,within
1717,Myzus persicae,95,rayyan-697471766,Positive genetic correlations among major life-history traits related to ecological success in the aphid Myzus persicae,2005,2002-2003,"Melbourne,Australia",lab,female,female,NA,NA,19,19,608,608,NA,NA,608,608,animal_model,genetic_line,no,broad,authors,adult,adult,daily fecundity 4 ,total offspring ,fertility,fertility,include,cor,0.553,0.244,se,NA,NA,NA,NA,NA,NA,rg,table 2,fertility,fertility,genotype,0.622692614,19,1,0.622692614,female,adult,Insecta,within
1719,Myzus persicae,95,rayyan-697471766,Positive genetic correlations among major life-history traits related to ecological success in the aphid Myzus persicae,2005,2002-2003,"Melbourne,Australia",lab,female,female,NA,NA,19,19,608,608,NA,NA,608,608,animal_model,genetic_line,no,broad,authors,adult,non_adult,daily fecundity 5,offspring size (hind tibia length of newborn first instar nymphs),fertility,size,include,cor,0.832,0.144,se,NA,NA,NA,NA,NA,NA,rg,table 2,fertility,size,genotype,1.194599783,19,1,1.194599783,female,cross,Insecta,between
1720,Myzus persicae,95,rayyan-697471766,Positive genetic correlations among major life-history traits related to ecological success in the aphid Myzus persicae,2005,2002-2003,"Melbourne,Australia",lab,female,female,NA,NA,19,19,608,608,NA,NA,608,608,animal_model,genetic_line,no,broad,authors,adult,adult,daily fecundity 3,daily fecundity 4 ,fertility,fertility,include,cor,-0.168,0.345,se,NA,NA,NA,NA,NA,NA,rg,table 2,fertility,fertility,genotype,-0.169607861,19,1,-0.169607861,female,adult,Insecta,within
1722,Myzus persicae,95,rayyan-697471766,Positive genetic correlations among major life-history traits related to ecological success in the aphid Myzus persicae,2005,2002-2003,"Melbourne,Australia",lab,female,female,NA,NA,19,19,608,608,NA,NA,608,608,animal_model,genetic_line,no,broad,authors,adult,non_adult,daily fecundity 5,offspring size (hind tibia length of newborn first instar nymphs),fertility,size,include,cor,0.107,0.482,se,NA,NA,NA,NA,NA,NA,rg,table 2,fertility,size,genotype,0.107411176,19,1,0.107411176,female,cross,Insecta,between
1723,Myzus persicae,95,rayyan-697471766,Positive genetic correlations among major life-history traits related to ecological success in the aphid Myzus persicae,2005,2002-2003,"Melbourne,Australia",lab,female,female,NA,NA,19,19,608,608,NA,NA,608,608,animal_model,genetic_line,no,broad,authors,adult,non_adult,daily fecundity 5,offspring size (hind tibia length of newborn first instar nymphs),fertility,size,include,cor,0.55,0.283,se,NA,NA,NA,NA,NA,NA,rg,table 2,fertility,size,genotype,0.618381314,19,1,0.618381314,female,cross,Insecta,between
1724,Myzus persicae,77,rayyan-697471690,Genetic variation and covariation of aphid life-history traits across unrelated host plants,2008,2003,"Melbourne, Autralia",lab,female,female,NA,NA,17,17,NA,NA,NA,NA,NA,NA,animal_model,genetic_line,no,broad,authors,adult,adult,"daily fecundity (for the second five-day interval, reproduction at max rate)","total offspring  (for the second five-day interval, reproduction at max rate)",fertility,fertility,include,cor,0.71,0.62,se,NA,NA,NA,NA,NA,NA,lambsquarters,table 2,fertility,fertility,genotype,0.887183863,17,1,0.887183863,female,adult,Insecta,within
1725,Myzus persicae,95,rayyan-697471766,Positive genetic correlations among major life-history traits related to ecological success in the aphid Myzus persicae,2005,2002-2003,"Melbourne,Australia",lab,female,female,NA,NA,19,19,608,608,NA,NA,608,608,animal_model,genetic_line,no,broad,authors,adult,adult,daily fecundity 3,daily fecundity 4 ,fertility,fertility,include,cor,0.586,0.265,se,NA,NA,NA,NA,NA,NA,rg,table 2,fertility,fertility,genotype,0.671552214,19,1,0.671552214,female,adult,Insecta,within
1726,Myzus persicae,95,rayyan-697471766,Positive genetic correlations among major life-history traits related to ecological success in the aphid Myzus persicae,2005,2002-2003,"Melbourne,Australia",lab,female,female,NA,NA,19,19,608,608,NA,NA,608,608,animal_model,genetic_line,no,broad,authors,adult,adult,daily fecundity 4,total offspring ,fertility,fertility,include,cor,0.98,0.041,se,NA,NA,NA,NA,NA,NA,rg,table 2,fertility,fertility,genotype,2.297559925,19,1,2.297559925,female,adult,Insecta,within
1728,Nematus brevivalvis,397,rayyan-697473009,Seasonally varying diet quality and the quantitative genetics of development time and body size in birch feeding insects,2001,NA,Finland,lab,male,male,NA,NA,NA,NA,20,20,NA,NA,349,349,animal_model,full_sib,no,broad,authors,non_adult,non_adult,development time,final larval mass,reverse_maturation,size,include,cor,0.854,0.087,se,NA,NA,NA,NA,NA,NA,species_3_covariance,figure 2a,maturation,size,family,1.270747062,20,-1,-1.270747062,male,non_adult,Insecta,between
1731,Nematus pravus,397,rayyan-697473009,Seasonally varying diet quality and the quantitative genetics of development time and body size in birch feeding insects,2001,NA,Finland,lab,male,male,NA,NA,NA,NA,18,18,NA,NA,268,268,animal_model,full_sib,no,broad,authors,non_adult,non_adult,development time,final larval mass,reverse_maturation,size,include,cor,0.143,0.183,se,NA,NA,NA,NA,NA,NA,species_6_covariance,figure 2a,maturation,size,family,0.143986873,18,-1,-0.143986873,male,non_adult,Insecta,between
1735,Nicrophorus pustulatus,240,rayyan-197247390,Quantitative genetics of growth and development time in the burying beetle Nicrophorus pustulatus in the presence and absence of post-hatching parental care,2002,1997,Kentucky,lab,both,both,NA,NA,NA,NA,162,169,61,64,637,649,animal_model,half_sib,no,narrow,authors,non_adult,non_adult,mass at 72 h (larval stage),development time (hatching to emergence),size,reverse_maturation,include,cor,-0.86,NA,NA,NA,NA,NA,NA,NA,NA,without_maternal_care_sire_variance,table 4,size,maturation,family,-1.293344672,162,-1,1.293344672,both,non_adult,Insecta,between
1736,Nicrophorus pustulatus,240,rayyan-197247390,Quantitative genetics of growth and development time in the burying beetle Nicrophorus pustulatus in the presence and absence of post-hatching parental care,2002,1997,Kentucky,lab,both,both,NA,NA,NA,NA,174,173,65,65,NA,661,animal_model,half_sib,no,narrow,authors,non_adult,non_adult,development time (hatching to dispersal),development time (larval wandering stage),reverse_maturation,reverse_maturation,include,cor,-0.02,NA,NA,NA,NA,NA,NA,NA,NA,without_maternal_care_sire_variance,table 4,maturation,maturation,family,-0.020002667,173,1,-0.020002667,both,non_adult,Insecta,within
1737,Nicrophorus pustulatus,240,rayyan-197247390,Quantitative genetics of growth and development time in the burying beetle Nicrophorus pustulatus in the presence and absence of post-hatching parental care,2002,1997,Kentucky,lab,both,both,NA,NA,NA,NA,169,169,64,64,636,649,animal_model,half_sib,no,narrow,authors,non_adult,non_adult,development time (in pupal chamber),development time (hatching to emergence),reverse_maturation,reverse_maturation,include,cor,0.57,NA,NA,NA,NA,NA,NA,NA,NA,without_maternal_care_sire_variance,table 4,maturation,maturation,family,0.647522845,169,1,0.647522845,both,non_adult,Insecta,within
1740,Nicrophorus pustulatus,240,rayyan-197247390,Quantitative genetics of growth and development time in the burying beetle Nicrophorus pustulatus in the presence and absence of post-hatching parental care,2002,1997,Kentucky,lab,both,both,NA,NA,NA,NA,173,169,65,64,661,649,animal_model,half_sib,no,narrow,authors,non_adult,non_adult,development time (larval wandering stage),development time (hatching to emergence),reverse_maturation,reverse_maturation,include,cor,0.26,NA,NA,NA,NA,NA,NA,NA,NA,without_maternal_care_sire_variance,table 4,maturation,maturation,family,0.266108407,169,1,0.266108407,both,non_adult,Insecta,within
1743,Nicrophorus pustulatus,240,rayyan-197247390,Quantitative genetics of growth and development time in the burying beetle Nicrophorus pustulatus in the presence and absence of post-hatching parental care,2002,1997,Kentucky,lab,both,both,NA,NA,NA,NA,162,169,61,64,637,636,animal_model,half_sib,no,narrow,authors,non_adult,non_adult,mass at 72 h (larval stage),development time (in pupal chamber),size,reverse_maturation,include,cor,-0.38,NA,NA,NA,NA,NA,NA,NA,NA,without_maternal_care_sire_variance,table 4,size,maturation,family,-0.40005965,162,-1,0.40005965,both,non_adult,Insecta,between
1744,Nicrophorus pustulatus,240,rayyan-197247390,Quantitative genetics of growth and development time in the burying beetle Nicrophorus pustulatus in the presence and absence of post-hatching parental care,2002,1997,Kentucky,lab,both,both,NA,NA,NA,NA,162,173,61,65,637,661,animal_model,half_sib,no,narrow,authors,non_adult,non_adult,mass at 72 h (larval stage),development time (larval wandering stage),size,reverse_maturation,include,cor,0.04,NA,NA,NA,NA,NA,NA,NA,NA,without_maternal_care_sire_variance,table 4,size,maturation,family,0.040021354,162,-1,-0.040021354,both,non_adult,Insecta,between
1745,Nicrophorus pustulatus,240,rayyan-197247390,Quantitative genetics of growth and development time in the burying beetle Nicrophorus pustulatus in the presence and absence of post-hatching parental care,2002,1997,Kentucky,lab,both,both,NA,NA,NA,NA,173,169,65,64,661,636,animal_model,half_sib,no,narrow,authors,non_adult,non_adult,development time (larval wandering stage),development time (in pupal chamber),reverse_maturation,reverse_maturation,include,cor,-0.43,NA,NA,NA,NA,NA,NA,NA,NA,without_maternal_care_sire_variance,table 4,maturation,maturation,family,-0.459896681,169,1,-0.459896681,both,non_adult,Insecta,within
1750,Nicrophorus pustulatus,240,rayyan-197247390,Quantitative genetics of growth and development time in the burying beetle Nicrophorus pustulatus in the presence and absence of post-hatching parental care,2002,1997,Kentucky,lab,both,both,NA,NA,NA,NA,174,174,65,65,2289,NA,sire_mean_correlation,half_sib,no,broad,authors,non_adult,non_adult,mass at larval dispersal,development time (hatching to dispersal),size,reverse_maturation,include,cor,-0.53,NA,NA,NA,NA,NA,NA,NA,NA,without_maternal_care_family_mean,table 4,size,maturation,family,-0.59014516,174,-1,0.59014516,both,non_adult,Insecta,between
1755,Nicrophorus pustulatus,240,rayyan-197247390,Quantitative genetics of growth and development time in the burying beetle Nicrophorus pustulatus in the presence and absence of post-hatching parental care,2002,1997,Kentucky,lab,both,both,NA,NA,NA,NA,174,173,65,65,2289,661,sire_mean_correlation,half_sib,no,broad,authors,non_adult,non_adult,mass at larval dispersal,development time (larval wandering stage),size,reverse_maturation,include,cor,0.01,NA,NA,NA,NA,NA,NA,NA,NA,without_maternal_care_family_mean,table 4,size,maturation,family,0.010000333,173,-1,-0.010000333,both,non_adult,Insecta,between
1757,Nicrophorus pustulatus,240,rayyan-197247390,Quantitative genetics of growth and development time in the burying beetle Nicrophorus pustulatus in the presence and absence of post-hatching parental care,2002,1997,Kentucky,lab,both,both,NA,NA,NA,NA,174,169,65,64,NA,649,animal_model,half_sib,no,narrow,authors,non_adult,non_adult,development time (hatching to dispersal),development time (hatching to emergence),reverse_maturation,reverse_maturation,include,cor,0.87,NA,NA,NA,NA,NA,NA,NA,NA,without_maternal_care_sire_variance,table 4,maturation,maturation,family,1.33307963,169,1,1.33307963,both,non_adult,Insecta,within
1760,Nicrophorus pustulatus,240,rayyan-197247390,Quantitative genetics of growth and development time in the burying beetle Nicrophorus pustulatus in the presence and absence of post-hatching parental care,2002,1997,Kentucky,lab,both,both,165,174,NA,NA,165,174,62,65,660,2165,sire_mean_correlation,half_sib,no,broad,authors,non_adult,non_adult,mass at hatching,mass at larval dispersal,size,size,include,cor,0.06,NA,NA,NA,NA,NA,NA,NA,NA,with_maternal_care_family_mean,table 4,size,size,family,0.060072156,165,1,0.060072156,both,non_adult,Insecta,within
1762,Nicrophorus pustulatus,240,rayyan-197247390,Quantitative genetics of growth and development time in the burying beetle Nicrophorus pustulatus in the presence and absence of post-hatching parental care,2002,1997,Kentucky,lab,both,both,NA,NA,NA,NA,174,169,65,64,2165,647,animal_model,half_sib,no,narrow,authors,non_adult,non_adult,mass at larval dispersal,development time (hatching to emergence),size,reverse_maturation,include,cor,-0.4,NA,NA,NA,NA,NA,NA,NA,NA,with_maternal_care_sire_variance,table 4,size,maturation,family,-0.42364893,169,-1,0.42364893,both,non_adult,Insecta,between
1763,Nicrophorus pustulatus,240,rayyan-197247390,Quantitative genetics of growth and development time in the burying beetle Nicrophorus pustulatus in the presence and absence of post-hatching parental care,2002,1997,Kentucky,lab,both,both,162,135,NA,NA,162,135,61,51,648,1643,sire_mean_correlation,half_sib,no,broad,authors,non_adult,adult,mass at 72 h (larval stage),mass at emergence,size,size,include,cor,0.42,NA,NA,NA,NA,NA,NA,NA,NA,with_maternal_care_family_mean,table 4,size,size,family,0.447692024,135,1,0.447692024,both,cross,Insecta,within
1764,Nicrophorus pustulatus,240,rayyan-197247390,Quantitative genetics of growth and development time in the burying beetle Nicrophorus pustulatus in the presence and absence of post-hatching parental care,2002,1997,Kentucky,lab,both,both,NA,NA,NA,NA,165,173,62,65,660,661,animal_model,half_sib,no,narrow,authors,non_adult,non_adult,mass at hatching,development time (larval wandering stage),size,reverse_maturation,include,cor,0.25,NA,NA,NA,NA,NA,NA,NA,NA,without_maternal_care_sire_variance,table 4,size,maturation,family,0.255412812,165,-1,-0.255412812,both,non_adult,Insecta,between
1765,Nicrophorus pustulatus,240,rayyan-197247390,Quantitative genetics of growth and development time in the burying beetle Nicrophorus pustulatus in the presence and absence of post-hatching parental care,2002,1997,Kentucky,lab,both,both,NA,NA,NA,NA,162,174,61,65,637,NA,animal_model,half_sib,no,narrow,authors,non_adult,non_adult,mass at 72 h (larval stage),development time (hatching to dispersal),size,reverse_maturation,include,cor,-0.89,NA,NA,NA,NA,NA,NA,NA,NA,without_maternal_care_sire_variance,table 4,size,maturation,family,-1.421925871,162,-1,1.421925871,both,non_adult,Insecta,between
1766,Nicrophorus pustulatus,240,rayyan-197247390,Quantitative genetics of growth and development time in the burying beetle Nicrophorus pustulatus in the presence and absence of post-hatching parental care,2002,1997,Kentucky,lab,both,both,NA,NA,NA,NA,173,169,65,64,668,639,sire_mean_correlation,half_sib,no,broad,authors,non_adult,non_adult,development time (larval wandering stage),development time (in pupal chamber),reverse_maturation,reverse_maturation,include,cor,-0.07,NA,NA,NA,NA,NA,NA,NA,NA,with_maternal_care_family_mean,table 4,maturation,maturation,family,-0.070114671,169,1,-0.070114671,both,non_adult,Insecta,within
1767,Nicrophorus pustulatus,240,rayyan-197247390,Quantitative genetics of growth and development time in the burying beetle Nicrophorus pustulatus in the presence and absence of post-hatching parental care,2002,1997,Kentucky,lab,both,both,NA,NA,NA,NA,173,169,65,64,668,647,sire_mean_correlation,half_sib,no,broad,authors,non_adult,non_adult,development time (larval wandering stage),development time (hatching to emergence),reverse_maturation,reverse_maturation,include,cor,0.52,NA,NA,NA,NA,NA,NA,NA,NA,with_maternal_care_family_mean,table 4,maturation,maturation,family,0.576339755,169,1,0.576339755,both,non_adult,Insecta,within
1768,Nicrophorus pustulatus,240,rayyan-197247390,Quantitative genetics of growth and development time in the burying beetle Nicrophorus pustulatus in the presence and absence of post-hatching parental care,2002,1997,Kentucky,lab,both,both,165,174,NA,NA,165,174,62,65,660,2289,sire_mean_correlation,half_sib,no,broad,authors,non_adult,non_adult,mass at hatching,mass at larval dispersal,size,size,include,cor,0.16,NA,NA,NA,NA,NA,NA,NA,NA,without_maternal_care_family_mean,table 4,size,size,family,0.161386696,165,1,0.161386696,both,non_adult,Insecta,within
1769,Nicrophorus pustulatus,240,rayyan-197247390,Quantitative genetics of growth and development time in the burying beetle Nicrophorus pustulatus in the presence and absence of post-hatching parental care,2002,1997,Kentucky,lab,both,both,NA,NA,NA,NA,174,169,65,64,2289,636,sire_mean_correlation,half_sib,no,broad,authors,non_adult,non_adult,mass at larval dispersal,development time (in pupal chamber),size,reverse_maturation,include,cor,0.39,NA,NA,NA,NA,NA,NA,NA,NA,without_maternal_care_family_mean,table 4,size,maturation,family,0.411800034,169,-1,-0.411800034,both,non_adult,Insecta,between
1770,Nicrophorus pustulatus,240,rayyan-197247390,Quantitative genetics of growth and development time in the burying beetle Nicrophorus pustulatus in the presence and absence of post-hatching parental care,2002,1997,Kentucky,lab,both,both,NA,NA,NA,NA,174,173,65,65,2165,668,sire_mean_correlation,half_sib,no,broad,authors,non_adult,non_adult,mass at larval dispersal,development time (larval wandering stage),size,reverse_maturation,include,cor,0.09,NA,NA,NA,NA,NA,NA,NA,NA,with_maternal_care_family_mean,table 4,size,maturation,family,0.090244188,173,-1,-0.090244188,both,non_adult,Insecta,between
1771,Nicrophorus pustulatus,240,rayyan-197247390,Quantitative genetics of growth and development time in the burying beetle Nicrophorus pustulatus in the presence and absence of post-hatching parental care,2002,1997,Kentucky,lab,both,both,NA,NA,NA,NA,174,169,65,64,NA,636,animal_model,half_sib,no,narrow,authors,non_adult,non_adult,development time (hatching to dispersal),development time (in pupal chamber),reverse_maturation,reverse_maturation,include,cor,0.43,NA,NA,NA,NA,NA,NA,NA,NA,without_maternal_care_sire_variance,table 4,maturation,maturation,family,0.459896681,169,1,0.459896681,both,non_adult,Insecta,within
1772,Nicrophorus pustulatus,240,rayyan-197247390,Quantitative genetics of growth and development time in the burying beetle Nicrophorus pustulatus in the presence and absence of post-hatching parental care,2002,1997,Kentucky,lab,both,both,174,135,NA,NA,174,135,65,51,2289,1664,sire_mean_correlation,half_sib,no,broad,authors,non_adult,adult,mass at larval dispersal,mass at emergence,size,size,include,cor,0.84,NA,NA,NA,NA,NA,NA,NA,NA,without_maternal_care_family_mean,table 4,size,size,family,1.221173518,135,1,1.221173518,both,cross,Insecta,within
1773,Nicrophorus pustulatus,240,rayyan-197247390,Quantitative genetics of growth and development time in the burying beetle Nicrophorus pustulatus in the presence and absence of post-hatching parental care,2002,1997,Kentucky,lab,both,both,174,169,NA,NA,174,169,65,64,NA,639,animal_model,half_sib,no,narrow,authors,non_adult,non_adult,development time (hatching to dispersal),development time (in pupal chamber),reverse_maturation,reverse_maturation,include,cor,0.37,NA,NA,NA,NA,NA,NA,NA,NA,with_maternal_care_sire_variance,table 4,maturation,maturation,family,0.3884231,169,1,0.3884231,both,non_adult,Insecta,within
1774,Nicrophorus pustulatus,240,rayyan-197247390,Quantitative genetics of growth and development time in the burying beetle Nicrophorus pustulatus in the presence and absence of post-hatching parental care,2002,1997,Kentucky,lab,both,both,162,174,NA,NA,162,174,61,65,648,2165,sire_mean_correlation,half_sib,no,broad,authors,non_adult,non_adult,mass at 72 h (larval stage),mass at larval dispersal,size,size,include,cor,0.55,NA,NA,NA,NA,NA,NA,NA,NA,with_maternal_care_family_mean,table 4,size,size,family,0.618381314,162,1,0.618381314,both,non_adult,Insecta,within
1775,Nicrophorus pustulatus,240,rayyan-197247390,Quantitative genetics of growth and development time in the burying beetle Nicrophorus pustulatus in the presence and absence of post-hatching parental care,2002,1997,Kentucky,lab,both,both,NA,NA,NA,NA,135,173,51,65,1643,668,sire_mean_correlation,half_sib,no,broad,authors,adult,non_adult,mass at emergence,development time (larval wandering stage),size,reverse_maturation,include,cor,-0.04,NA,NA,NA,NA,NA,NA,NA,NA,with_maternal_care_family_mean,table 4,size,maturation,family,-0.040021354,135,-1,0.040021354,both,cross,Insecta,between
1776,Nicrophorus pustulatus,240,rayyan-197247390,Quantitative genetics of growth and development time in the burying beetle Nicrophorus pustulatus in the presence and absence of post-hatching parental care,2002,1997,Kentucky,lab,both,both,NA,NA,NA,NA,135,169,51,64,1643,647,sire_mean_correlation,half_sib,no,broad,authors,adult,non_adult,mass at emergence,development time (hatching to emergence),size,reverse_maturation,include,cor,0.3,NA,NA,NA,NA,NA,NA,NA,NA,with_maternal_care_family_mean,table 4,size,maturation,family,0.309519604,135,-1,-0.309519604,both,cross,Insecta,between
1777,Nicrophorus pustulatus,240,rayyan-197247390,Quantitative genetics of growth and development time in the burying beetle Nicrophorus pustulatus in the presence and absence of post-hatching parental care,2002,1997,Kentucky,lab,both,both,174,135,NA,NA,174,135,65,51,2165,1643,sire_mean_correlation,half_sib,no,broad,authors,non_adult,adult,mass at larval dispersal,mass at emergence,size,size,include,cor,0.85,NA,NA,NA,NA,NA,NA,NA,NA,with_maternal_care_family_mean,table 4,size,size,family,1.256152812,135,1,1.256152812,both,cross,Insecta,within
1780,Nicrophorus pustulatus,240,rayyan-197247390,Quantitative genetics of growth and development time in the burying beetle Nicrophorus pustulatus in the presence and absence of post-hatching parental care,2002,1997,Kentucky,lab,both,both,NA,NA,NA,NA,162,173,61,65,648,668,sire_mean_correlation,half_sib,no,broad,authors,non_adult,non_adult,mass at 72 h (larval stage),development time (larval wandering stage),size,reverse_maturation,include,cor,0.01,NA,NA,NA,NA,NA,NA,NA,NA,with_maternal_care_family_mean,table 4,size,maturation,family,0.010000333,162,-1,-0.010000333,both,non_adult,Insecta,between
1781,Nicrophorus pustulatus,240,rayyan-197247390,Quantitative genetics of growth and development time in the burying beetle Nicrophorus pustulatus in the presence and absence of post-hatching parental care,2002,1997,Kentucky,lab,both,both,165,135,NA,NA,165,135,62,51,660,1664,animal_model,half_sib,no,narrow,authors,non_adult,adult,mass at hatching,mass at emergence,size,size,include,cor,NA,NA,NA,NA,NA,NA,NA,NA,NA,without_maternal_care_sire_variance,table 4,size,size,family,NA,135,1,NA,both,cross,Insecta,within
1783,Nicrophorus pustulatus,240,rayyan-197247390,Quantitative genetics of growth and development time in the burying beetle Nicrophorus pustulatus in the presence and absence of post-hatching parental care,2002,1997,Kentucky,lab,both,both,162,174,NA,NA,162,174,61,65,637,2289,sire_mean_correlation,half_sib,no,broad,authors,non_adult,non_adult,mass at 72 h (larval stage),mass at larval dispersal,size,size,include,cor,0.52,NA,NA,NA,NA,NA,NA,NA,NA,without_maternal_care_family_mean,table 4,size,size,family,0.576339755,162,1,0.576339755,both,non_adult,Insecta,within
1784,Nicrophorus pustulatus,240,rayyan-197247390,Quantitative genetics of growth and development time in the burying beetle Nicrophorus pustulatus in the presence and absence of post-hatching parental care,2002,1997,Kentucky,lab,both,both,165,162,NA,NA,165,162,62,61,660,648,animal_model,half_sib,no,narrow,authors,non_adult,non_adult,mass at hatching,mass at 72 h (larval stage),size,size,include,cor,0.35,NA,NA,NA,NA,NA,NA,NA,NA,with_maternal_care_sire_variance,table 4,size,size,family,0.365443754,162,1,0.365443754,both,non_adult,Insecta,within
1785,Nicrophorus pustulatus,240,rayyan-197247390,Quantitative genetics of growth and development time in the burying beetle Nicrophorus pustulatus in the presence and absence of post-hatching parental care,2002,1997,Kentucky,lab,both,both,NA,NA,NA,NA,174,169,65,64,2289,649,sire_mean_correlation,half_sib,no,broad,authors,non_adult,non_adult,mass at larval dispersal,development time (hatching to emergence),size,reverse_maturation,include,cor,-0.08,NA,NA,NA,NA,NA,NA,NA,NA,without_maternal_care_family_mean,table 4,size,maturation,family,-0.080171325,169,-1,0.080171325,both,non_adult,Insecta,between
1786,Nicrophorus pustulatus,240,rayyan-197247390,Quantitative genetics of growth and development time in the burying beetle Nicrophorus pustulatus in the presence and absence of post-hatching parental care,2002,1997,Kentucky,lab,both,both,NA,NA,NA,NA,135,174,51,65,1664,NA,sire_mean_correlation,half_sib,no,broad,authors,adult,non_adult,mass at emergence,development time (hatching to dispersal),size,reverse_maturation,include,cor,-0.36,NA,NA,NA,NA,NA,NA,NA,NA,without_maternal_care_family_mean,table 4,size,maturation,family,-0.376885901,135,-1,0.376885901,both,cross,Insecta,between
1787,Nicrophorus pustulatus,240,rayyan-197247390,Quantitative genetics of growth and development time in the burying beetle Nicrophorus pustulatus in the presence and absence of post-hatching parental care,2002,1997,Kentucky,lab,both,both,165,135,NA,NA,165,135,62,51,660,1643,sire_mean_correlation,half_sib,no,broad,authors,non_adult,adult,mass at hatching,mass at emergence,size,size,include,cor,-0.01,NA,NA,NA,NA,NA,NA,NA,NA,with_maternal_care_family_mean,table 4,size,size,family,-0.010000333,135,1,-0.010000333,both,cross,Insecta,within
1788,Nicrophorus pustulatus,240,rayyan-197247390,Quantitative genetics of growth and development time in the burying beetle Nicrophorus pustulatus in the presence and absence of post-hatching parental care,2002,1997,Kentucky,lab,both,both,NA,NA,NA,NA,135,169,51,64,1664,636,sire_mean_correlation,half_sib,no,broad,authors,adult,non_adult,mass at emergence,development time (in pupal chamber),size,reverse_maturation,include,cor,0.25,NA,NA,NA,NA,NA,NA,NA,NA,without_maternal_care_family_mean,table 4,size,maturation,family,0.255412812,135,-1,-0.255412812,both,cross,Insecta,between
1789,Nicrophorus pustulatus,240,rayyan-197247390,Quantitative genetics of growth and development time in the burying beetle Nicrophorus pustulatus in the presence and absence of post-hatching parental care,2002,1997,Kentucky,lab,both,both,NA,NA,NA,NA,135,169,51,64,1664,649,sire_mean_correlation,half_sib,no,broad,authors,adult,non_adult,mass at emergence,development time (hatching to emergence),size,reverse_maturation,include,cor,0.01,NA,NA,NA,NA,NA,NA,NA,NA,without_maternal_care_family_mean,table 4,size,maturation,family,0.010000333,135,-1,-0.010000333,both,cross,Insecta,between
1790,Nicrophorus pustulatus,240,rayyan-197247390,Quantitative genetics of growth and development time in the burying beetle Nicrophorus pustulatus in the presence and absence of post-hatching parental care,2002,1997,Kentucky,lab,both,both,NA,NA,NA,NA,165,174,62,65,660,NA,animal_model,half_sib,no,narrow,authors,non_adult,non_adult,mass at hatching,development time (hatching to dispersal),size,reverse_maturation,include,cor,-0.12,NA,NA,NA,NA,NA,NA,NA,NA,without_maternal_care_sire_variance,table 4,size,maturation,family,-0.120581028,165,-1,0.120581028,both,non_adult,Insecta,between
1792,Nicrophorus pustulatus,240,rayyan-197247390,Quantitative genetics of growth and development time in the burying beetle Nicrophorus pustulatus in the presence and absence of post-hatching parental care,2002,1997,Kentucky,lab,both,both,NA,NA,NA,NA,165,169,62,64,660,636,animal_model,half_sib,no,narrow,authors,non_adult,non_adult,mass at hatching,development time (in pupal chamber),size,reverse_maturation,include,cor,0.19,NA,NA,NA,NA,NA,NA,NA,NA,without_maternal_care_sire_variance,table 4,size,maturation,family,0.192337169,165,-1,-0.192337169,both,non_adult,Insecta,between
1794,Nicrophorus pustulatus,240,rayyan-197247390,Quantitative genetics of growth and development time in the burying beetle Nicrophorus pustulatus in the presence and absence of post-hatching parental care,2002,1997,Kentucky,lab,both,both,165,162,NA,NA,165,162,62,61,660,637,animal_model,half_sib,no,narrow,authors,non_adult,non_adult,mass at hatching,mass at 72 h (larval stage),size,size,include,cor,0.04,NA,NA,NA,NA,NA,NA,NA,NA,without_maternal_care_sire_variance,table 4,size,size,family,0.040021354,162,1,0.040021354,both,non_adult,Insecta,within
1796,Nicrophorus pustulatus,240,rayyan-197247390,Quantitative genetics of growth and development time in the burying beetle Nicrophorus pustulatus in the presence and absence of post-hatching parental care,2002,1997,Kentucky,lab,both,both,NA,NA,NA,NA,165,174,62,65,660,NA,animal_model,half_sib,no,narrow,authors,non_adult,non_adult,mass at hatching,development time (hatching to dispersal),size,reverse_maturation,include,cor,-0.28,NA,NA,NA,NA,NA,NA,NA,NA,with_maternal_care_sire_variance,table 4,size,maturation,family,-0.287682072,165,-1,0.287682072,both,non_adult,Insecta,between
1798,Nicrophorus pustulatus,240,rayyan-197247390,Quantitative genetics of growth and development time in the burying beetle Nicrophorus pustulatus in the presence and absence of post-hatching parental care,2002,1997,Kentucky,lab,both,both,NA,NA,NA,NA,135,174,51,65,1643,NA,sire_mean_correlation,half_sib,no,broad,authors,adult,non_adult,mass at emergence,development time (hatching to dispersal),size,reverse_maturation,include,cor,0.16,NA,NA,NA,NA,NA,NA,NA,NA,with_maternal_care_family_mean,table 4,size,maturation,family,0.161386696,135,-1,-0.161386696,both,cross,Insecta,between
1799,Nicrophorus pustulatus,240,rayyan-197247390,Quantitative genetics of growth and development time in the burying beetle Nicrophorus pustulatus in the presence and absence of post-hatching parental care,2002,1997,Kentucky,lab,both,both,NA,NA,NA,NA,165,169,62,64,660,647,animal_model,half_sib,no,narrow,authors,non_adult,non_adult,mass at hatching,development time (hatching to emergence),size,reverse_maturation,include,cor,0.01,NA,NA,NA,NA,NA,NA,NA,NA,with_maternal_care_sire_variance,table 4,size,maturation,family,0.010000333,165,-1,-0.010000333,both,non_adult,Insecta,between
1800,Nicrophorus pustulatus,240,rayyan-197247390,Quantitative genetics of growth and development time in the burying beetle Nicrophorus pustulatus in the presence and absence of post-hatching parental care,2002,1997,Kentucky,lab,both,both,NA,NA,NA,NA,135,173,51,65,1664,661,sire_mean_correlation,half_sib,no,broad,authors,adult,non_adult,mass at emergence,development time (larval wandering stage),size,reverse_maturation,include,cor,0.15,NA,NA,NA,NA,NA,NA,NA,NA,without_maternal_care_family_mean,table 4,size,maturation,family,0.151140436,135,-1,-0.151140436,both,cross,Insecta,between
1801,Nicrophorus pustulatus,240,rayyan-197247390,Quantitative genetics of growth and development time in the burying beetle Nicrophorus pustulatus in the presence and absence of post-hatching parental care,2002,1997,Kentucky,lab,both,both,NA,NA,NA,NA,162,169,61,64,648,639,animal_model,half_sib,no,narrow,authors,non_adult,non_adult,mass at 72 h (larval stage),development time (in pupal chamber),size,reverse_maturation,include,cor,-0.29,NA,NA,NA,NA,NA,NA,NA,NA,with_maternal_care_sire_variance,table 4,size,maturation,family,-0.298566264,162,-1,0.298566264,both,non_adult,Insecta,between
1804,Nicrophorus pustulatus,240,rayyan-197247390,Quantitative genetics of growth and development time in the burying beetle Nicrophorus pustulatus in the presence and absence of post-hatching parental care,2002,1997,Kentucky,lab,both,both,NA,NA,NA,NA,165,173,62,65,660,668,sire_mean_correlation,half_sib,no,broad,authors,non_adult,non_adult,mass at hatching,development time (larval wandering stage),size,reverse_maturation,include,cor,0.18,NA,NA,NA,NA,NA,NA,NA,NA,with_maternal_care_family_mean,table 4,size,maturation,family,0.181982689,165,-1,-0.181982689,both,non_adult,Insecta,between
1806,Nicrophorus pustulatus,240,rayyan-197247390,Quantitative genetics of growth and development time in the burying beetle Nicrophorus pustulatus in the presence and absence of post-hatching parental care,2002,1997,Kentucky,lab,both,both,NA,NA,NA,NA,165,169,62,64,660,639,animal_model,half_sib,no,narrow,authors,non_adult,non_adult,mass at hatching,development time (in pupal chamber),size,reverse_maturation,include,cor,0.03,NA,NA,NA,NA,NA,NA,NA,NA,with_maternal_care_sire_variance,table 4,size,maturation,family,0.030009005,165,-1,-0.030009005,both,non_adult,Insecta,between
1807,Nicrophorus pustulatus,240,rayyan-197247390,Quantitative genetics of growth and development time in the burying beetle Nicrophorus pustulatus in the presence and absence of post-hatching parental care,2002,1997,Kentucky,lab,both,both,NA,NA,NA,NA,162,169,61,64,648,647,animal_model,half_sib,no,narrow,authors,non_adult,non_adult,mass at 72 h (larval stage),development time (hatching to emergence),size,reverse_maturation,include,cor,-0.08,NA,NA,NA,NA,NA,NA,NA,NA,with_maternal_care_sire_variance,table 4,size,maturation,family,-0.080171325,162,-1,0.080171325,both,non_adult,Insecta,between
1808,Nicrophorus pustulatus,240,rayyan-197247390,Quantitative genetics of growth and development time in the burying beetle Nicrophorus pustulatus in the presence and absence of post-hatching parental care,2002,1997,Kentucky,lab,both,both,162,135,NA,NA,162,135,61,51,637,1664,animal_model,half_sib,no,narrow,authors,non_adult,adult,mass at 72 h (larval stage),mass at emergence,size,size,include,cor,0.03,NA,NA,NA,NA,NA,NA,NA,NA,without_maternal_care_sire_variance,table 4,size,size,family,0.030009005,135,1,0.030009005,both,cross,Insecta,within
1810,Nicrophorus pustulatus,240,rayyan-197247390,Quantitative genetics of growth and development time in the burying beetle Nicrophorus pustulatus in the presence and absence of post-hatching parental care,2002,1997,Kentucky,lab,both,both,NA,NA,NA,NA,174,169,65,64,2165,639,animal_model,half_sib,no,narrow,authors,non_adult,non_adult,mass at larval dispersal,development time (in pupal chamber),size,reverse_maturation,include,cor,-0.72,NA,NA,NA,NA,NA,NA,NA,NA,with_maternal_care_sire_variance,table 4,size,maturation,family,-0.907644983,169,-1,0.907644983,both,non_adult,Insecta,between
1811,Nicrophorus pustulatus,240,rayyan-197247390,Quantitative genetics of growth and development time in the burying beetle Nicrophorus pustulatus in the presence and absence of post-hatching parental care,2002,1997,Kentucky,lab,both,both,NA,NA,NA,NA,169,169,64,64,639,647,animal_model,half_sib,no,narrow,authors,non_adult,non_adult,development time (in pupal chamber),development time (hatching to emergence),reverse_maturation,reverse_maturation,include,cor,0.84,NA,NA,NA,NA,NA,NA,NA,NA,with_maternal_care_sire_variance,table 4,maturation,maturation,family,1.221173518,169,1,1.221173518,both,non_adult,Insecta,within
1812,Nicrophorus pustulatus,240,rayyan-197247390,Quantitative genetics of growth and development time in the burying beetle Nicrophorus pustulatus in the presence and absence of post-hatching parental care,2002,1997,Kentucky,lab,both,both,NA,NA,NA,NA,135,169,51,64,1643,639,sire_mean_correlation,half_sib,no,broad,authors,adult,non_adult,mass at emergence,development time (in pupal chamber),size,reverse_maturation,include,cor,0.24,NA,NA,NA,NA,NA,NA,NA,NA,with_maternal_care_family_mean,table 4,size,maturation,family,0.244774113,135,-1,-0.244774113,both,cross,Insecta,between
1813,Nicrophorus pustulatus,240,rayyan-197247390,Quantitative genetics of growth and development time in the burying beetle Nicrophorus pustulatus in the presence and absence of post-hatching parental care,2002,1997,Kentucky,lab,both,both,NA,NA,NA,NA,162,174,61,65,648,NA,animal_model,half_sib,no,narrow,authors,non_adult,non_adult,mass at 72 h (larval stage),development time (hatching to dispersal),size,reverse_maturation,include,cor,-0.6,NA,NA,NA,NA,NA,NA,NA,NA,with_maternal_care_sire_variance,table 4,size,maturation,family,-0.693147181,162,-1,0.693147181,both,non_adult,Insecta,between
1814,Nicrophorus pustulatus,240,rayyan-197247390,Quantitative genetics of growth and development time in the burying beetle Nicrophorus pustulatus in the presence and absence of post-hatching parental care,2002,1997,Kentucky,lab,both,both,NA,NA,NA,NA,174,169,65,64,NA,647,animal_model,half_sib,no,narrow,authors,non_adult,non_adult,development time (hatching to dispersal),development time (hatching to emergence),reverse_maturation,reverse_maturation,include,cor,0.76,NA,NA,NA,NA,NA,NA,NA,NA,with_maternal_care_sire_variance,table 4,maturation,maturation,family,0.996215082,169,1,0.996215082,both,non_adult,Insecta,within
1815,Nicrophorus pustulatus,240,rayyan-197247390,Quantitative genetics of growth and development time in the burying beetle Nicrophorus pustulatus in the presence and absence of post-hatching parental care,2002,1997,Kentucky,lab,both,both,NA,NA,NA,NA,174,173,65,65,NA,668,sire_mean_correlation,half_sib,no,broad,authors,non_adult,non_adult,development time (hatching to dispersal),development time (larval wandering stage),reverse_maturation,reverse_maturation,include,cor,-0.16,NA,NA,NA,NA,NA,NA,NA,NA,with_maternal_care_family_mean,table 4,maturation,maturation,family,-0.161386696,173,1,-0.161386696,both,non_adult,Insecta,within
1816,Nicrophorus pustulatus,240,rayyan-197247390,Quantitative genetics of growth and development time in the burying beetle Nicrophorus pustulatus in the presence and absence of post-hatching parental care,2002,1997,Kentucky,lab,both,both,NA,NA,NA,NA,174,174,65,65,2165,NA,animal_model,half_sib,no,narrow,authors,non_adult,non_adult,mass at larval dispersal,development time (hatching to dispersal),size,reverse_maturation,include,cor,-0.37,NA,NA,NA,NA,NA,NA,NA,NA,with_maternal_care_sire_variance,table 4,size,maturation,family,-0.3884231,174,-1,0.3884231,both,non_adult,Insecta,between
1817,Oikopleura dioica,195,rayyan-197247199,Heritability of morphological and life history traits in a pelagic tunicate,2011,2005,"Gijón, Spain",lab,both,both,39,39,NA,NA,39,39,13,13,390,390,animal_model,full/half_sib,no,narrow,authors,adult,adult,house size,tail length,size,size,include,cor,0.797,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-197247199,table 3,size,size,family,1.090333954,39,1,1.090333954,both,adult,Appendicularia,within
1818,Oikopleura dioica,195,rayyan-197247199,Heritability of morphological and life history traits in a pelagic tunicate,2011,2005,"Gijón, Spain",lab,both,female,39,39,NA,NA,39,39,13,13,390,390,animal_model,full/half_sib,no,narrow,authors,both,adult,lifespan (from embryo to death),clutch size,survival,fertility,include,cor,0.142,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-197247199,table 3,survival,fertility,family,0.142966145,39,1,0.142966145,female,cross,Appendicularia,between
1819,Oikopleura dioica,195,rayyan-197247199,Heritability of morphological and life history traits in a pelagic tunicate,2011,2005,"Gijón, Spain",lab,both,both,39,39,NA,NA,39,39,13,13,390,390,animal_model,full/half_sib,no,narrow,authors,adult,adult,trunk length,tail length,size,size,include,cor,0.917,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-197247199,table 3,size,size,family,1.569838068,39,1,1.569838068,both,adult,Appendicularia,within
1821,Oikopleura dioica,195,rayyan-197247199,Heritability of morphological and life history traits in a pelagic tunicate,2011,2005,"Gijón, Spain",lab,female,both,39,39,NA,NA,39,39,13,13,390,390,animal_model,full/half_sib,no,narrow,authors,adult,adult,clutch size,tail length,fertility,size,include,cor,-0.2,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-197247199,table 3,fertility,size,family,-0.202732554,39,1,-0.202732554,female,adult,Appendicularia,between
1822,Oikopleura dioica,195,rayyan-197247199,Heritability of morphological and life history traits in a pelagic tunicate,2011,2005,"Gijón, Spain",lab,female,both,39,39,NA,NA,39,39,13,13,390,390,animal_model,full/half_sib,no,narrow,authors,adult,adult,clutch size,trunk length,fertility,size,include,cor,-0.018,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-197247199,table 3,fertility,size,family,-0.018001944,39,1,-0.018001944,female,adult,Appendicularia,between
1823,Oikopleura dioica,195,rayyan-197247199,Heritability of morphological and life history traits in a pelagic tunicate,2011,2005,"Gijón, Spain",lab,both,both,39,39,NA,NA,39,39,13,13,390,390,animal_model,full/half_sib,no,narrow,authors,adult,adult,trunk length,house size,size,size,include,cor,0.697,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-197247199,table 3,size,size,family,0.86144223,39,1,0.86144223,both,adult,Appendicularia,within
1826,Oikopleura dioica,195,rayyan-197247199,Heritability of morphological and life history traits in a pelagic tunicate,2011,2005,"Gijón, Spain",lab,both,both,39,39,NA,NA,39,39,13,13,390,390,animal_model,full/half_sib,no,narrow,authors,both,adult,lifespan (from embryo to death),tail length,survival,size,include,cor,0.996,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-197247199,table 3,survival,size,family,3.106303048,39,1,3.106303048,both,cross,Appendicularia,between
1828,Oikopleura dioica,195,rayyan-197247199,Heritability of morphological and life history traits in a pelagic tunicate,2011,2005,"Gijón, Spain",lab,female,both,39,39,NA,NA,39,39,13,13,390,390,animal_model,full/half_sib,no,narrow,authors,adult,adult,clutch size,house size,fertility,size,include,cor,-0.563,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-197247199,table 3,fertility,size,family,-0.637214568,39,1,-0.637214568,female,adult,Appendicularia,between
1830,Oikopleura dioica,195,rayyan-197247199,Heritability of morphological and life history traits in a pelagic tunicate,2011,2005,"Gijón, Spain",lab,both,both,39,39,NA,NA,39,39,13,13,390,390,animal_model,full/half_sib,no,narrow,authors,both,adult,lifespan (from embryo to death),trunk length,survival,size,include,cor,0.935,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-197247199,table 3,survival,size,family,1.696737668,39,1,1.696737668,both,cross,Appendicularia,between
1831,Oikopleura dioica,195,rayyan-197247199,Heritability of morphological and life history traits in a pelagic tunicate,2011,2005,"Gijón, Spain",lab,both,both,39,39,NA,NA,39,39,13,13,390,390,animal_model,full/half_sib,no,narrow,authors,both,adult,lifespan (from embryo to death),house size,survival,size,include,cor,0.811,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-197247199,table 3,survival,size,family,1.129943721,39,1,1.129943721,both,cross,Appendicularia,between
1833,Oncorhynchus mykiss,47,rayyan-697471388,Quantitative genetics of migration-related traits in rainbow and steelhead trout,2015,1996-2004,southeastern Alaska,field,both,both,NA,NA,NA,NA,NA,NA,NA,NA,15514,15514,animal_model,pedigree,no,narrow,authors,both,both,Instantaneous growth rate in weight from month 12 to 15,fork length at month 24,growth,size,include,cor,0.687,0.114,se,NA,NA,NA,NA,NA,NA,rayyan-697471388,table s2,growth,size,pedigree,0.842251946,15514,1,0.842251946,both,both,Actinopteri,between
1834,Oncorhynchus mykiss,47,rayyan-697471388,Quantitative genetics of migration-related traits in rainbow and steelhead trout,2015,1996-2004,southeastern Alaska,field,both,both,NA,NA,NA,NA,NA,NA,NA,NA,15514,15514,animal_model,pedigree,no,narrow,authors,both,both,Instantaneous growth rate in weight from month 12 to 15,weight at month 24,growth,size,include,cor,0.763,0.117,se,NA,NA,NA,NA,NA,NA,rayyan-697471388,table s2,growth,size,pedigree,1.003356021,15514,1,1.003356021,both,both,Actinopteri,between
1835,Oncorhynchus mykiss,47,rayyan-697471388,Quantitative genetics of migration-related traits in rainbow and steelhead trout,2015,1996-2004,southeastern Alaska,field,both,both,NA,NA,NA,NA,NA,NA,NA,NA,15507,15507,animal_model,pedigree,no,narrow,authors,both,both,Instantaneous growth rate in weight from month 12 to 15,body condition factor (body length to weight) at month 24,growth,size,include,cor,-0.027,0.129,se,NA,NA,NA,NA,NA,NA,rayyan-697471388,table s2,growth,size,pedigree,-0.027006564,15507,1,-0.027006564,both,both,Actinopteri,between
1836,Oncorhynchus mykiss,47,rayyan-697471388,Quantitative genetics of migration-related traits in rainbow and steelhead trout,2015,1996-2004,southeastern Alaska,field,both,both,NA,NA,NA,NA,NA,NA,NA,NA,15014,15014,animal_model,pedigree,no,narrow,authors,non_adult,both,smolt or mature/parr at month 12,body condition factor (body length to weight) at month 12,maturation,size,include,cor,-0.579,"[-0.85, -0.21]",95CI,NA,NA,NA,NA,NA,NA,rayyan-697471388,table s2,maturation,size,pedigree,-0.66095709,15014,1,-0.66095709,both,cross,Actinopteri,between
1837,Oncorhynchus mykiss,47,rayyan-697471388,Quantitative genetics of migration-related traits in rainbow and steelhead trout,2015,1996-2004,southeastern Alaska,field,both,both,NA,NA,NA,NA,NA,NA,NA,NA,14968,14968,animal_model,pedigree,no,narrow,authors,non_adult,both,smolt or mature/parr at month 12,fork length at month 15,maturation,size,include,cor,0.44,"[0.30, 0.635]",95CI,NA,NA,NA,NA,NA,NA,rayyan-697471388,table s2,maturation,size,pedigree,0.472230804,14968,1,0.472230804,both,cross,Actinopteri,between
1838,Oncorhynchus mykiss,47,rayyan-697471388,Quantitative genetics of migration-related traits in rainbow and steelhead trout,2015,1996-2004,southeastern Alaska,field,both,both,NA,NA,NA,NA,NA,NA,NA,NA,14953,14953,animal_model,pedigree,no,narrow,authors,non_adult,both,smolt or mature/parr at month 12,weight at month 15,maturation,size,include,cor,0.35,"[-0.03, 0.51]",95CI,NA,NA,NA,NA,NA,NA,rayyan-697471388,table s2,maturation,size,pedigree,0.365443754,14953,1,0.365443754,both,cross,Actinopteri,between
1839,Oncorhynchus mykiss,47,rayyan-697471388,Quantitative genetics of migration-related traits in rainbow and steelhead trout,2015,1996-2004,southeastern Alaska,field,both,both,NA,NA,NA,NA,NA,NA,NA,NA,15635,15635,animal_model,pedigree,no,narrow,authors,both,both,fork length at month 24,weight at month 24,size,size,include,cor,0.943,0.02,se,NA,NA,NA,NA,NA,NA,rayyan-697471388,table s2,size,size,pedigree,1.764468591,15635,1,1.764468591,both,both,Actinopteri,within
1840,Oncorhynchus mykiss,47,rayyan-697471388,Quantitative genetics of migration-related traits in rainbow and steelhead trout,2015,1996-2004,southeastern Alaska,field,both,both,NA,NA,NA,NA,NA,NA,NA,NA,15504,15504,animal_model,pedigree,no,narrow,authors,both,both,Instantaneous growth rate in weight from month 12 to 15,Instantaneous growth rate in length from month 15 to 24,growth,growth,include,cor,0.346,0.154,se,NA,NA,NA,NA,NA,NA,rayyan-697471388,table s2,growth,growth,pedigree,0.360892579,15504,1,0.360892579,both,both,Actinopteri,within
1841,Oncorhynchus mykiss,47,rayyan-697471388,Quantitative genetics of migration-related traits in rainbow and steelhead trout,2015,1996-2004,southeastern Alaska,field,both,both,NA,NA,NA,NA,NA,NA,NA,NA,15514,15514,animal_model,pedigree,no,narrow,authors,both,both,Instantaneous growth rate in weight from month 12 to 15,Instantaneous growth rate in weightfrom month 15 to 24,growth,growth,include,cor,0.232,0.181,se,NA,NA,NA,NA,NA,NA,rayyan-697471388,table s2,growth,growth,pedigree,0.236302205,15514,1,0.236302205,both,both,Actinopteri,within
1842,Oncorhynchus mykiss,47,rayyan-697471388,Quantitative genetics of migration-related traits in rainbow and steelhead trout,2015,1996-2004,southeastern Alaska,field,both,both,NA,NA,NA,NA,NA,NA,NA,NA,15008,15008,animal_model,pedigree,no,narrow,authors,non_adult,both,smolt or mature/parr at month 12,fork length at month 24,maturation,size,include,cor,0.832,"[0.72, 0.91]",95CI,NA,NA,NA,NA,NA,NA,rayyan-697471388,table s2,maturation,size,pedigree,1.194599783,15008,1,1.194599783,both,cross,Actinopteri,between
1843,Oncorhynchus mykiss,47,rayyan-697471388,Quantitative genetics of migration-related traits in rainbow and steelhead trout,2015,1996-2004,southeastern Alaska,field,both,both,NA,NA,NA,NA,NA,NA,NA,NA,1702,1702,animal_model,pedigree,no,narrow,authors,non_adult,both,smolt or mature/parr at month 12,measure of overall body at month 24,maturation,size,include,cor,0.316,"[0.10, 0.63]",95CI,NA,NA,NA,NA,NA,NA,rayyan-697471388,table s2,maturation,size,pedigree,0.327197097,1702,1,0.327197097,both,cross,Actinopteri,between
1844,Oncorhynchus mykiss,47,rayyan-697471388,Quantitative genetics of migration-related traits in rainbow and steelhead trout,2015,1996-2004,southeastern Alaska,field,both,both,NA,NA,NA,NA,NA,NA,NA,NA,1972,1972,animal_model,pedigree,no,narrow,authors,both,both,weight at month 15,measure of overall body at month 24,size,size,include,cor,0.667,0.118,se,NA,NA,NA,NA,NA,NA,rayyan-697471388,table s2,size,size,pedigree,0.805319196,1972,1,0.805319196,both,both,Actinopteri,within
1845,Oncorhynchus mykiss,47,rayyan-697471388,Quantitative genetics of migration-related traits in rainbow and steelhead trout,2015,1996-2004,southeastern Alaska,field,both,both,NA,NA,NA,NA,NA,NA,NA,NA,15576,15576,animal_model,pedigree,no,narrow,authors,non_adult,both,mature or parr/indeterminate/smolt at month 12,weight at month 12,maturation,size,include,cor,0.098,"[-0.12, 0.51]",95CI,NA,NA,NA,NA,NA,NA,rayyan-697471388,table s2,maturation,size,pedigree,0.098315551,15576,1,0.098315551,both,cross,Actinopteri,between
1846,Oncorhynchus mykiss,47,rayyan-697471388,Quantitative genetics of migration-related traits in rainbow and steelhead trout,2015,1996-2004,southeastern Alaska,field,both,both,NA,NA,NA,NA,NA,NA,NA,NA,15569,15569,animal_model,pedigree,no,narrow,authors,non_adult,both,mature or parr/indeterminate/smolt at month 12,body condition factor (body length to weight) at month 12,maturation,size,include,cor,0.646,"[0.332, 0.848]",95CI,NA,NA,NA,NA,NA,NA,rayyan-697471388,table s2,maturation,size,pedigree,0.768403234,15569,1,0.768403234,both,cross,Actinopteri,between
1847,Oncorhynchus mykiss,47,rayyan-697471388,Quantitative genetics of migration-related traits in rainbow and steelhead trout,2015,1996-2004,southeastern Alaska,field,both,both,NA,NA,NA,NA,NA,NA,NA,NA,15581,15581,animal_model,pedigree,no,narrow,authors,non_adult,both,mature or parr/indeterminate/smolt at month 12,fork length at month 15,maturation,size,include,cor,0.033,"[-0.36, 0.11]",95CI,NA,NA,NA,NA,NA,NA,rayyan-697471388,table s2,maturation,size,pedigree,0.033011987,15581,1,0.033011987,both,cross,Actinopteri,between
1848,Oncorhynchus mykiss,60,rayyan-697471502,Untangling the positive genetic correlation between rainbow trout growth and survival,2012,1995-2004,Central Finland,field,both,both,1568,2231,NA,NA,852,1401,623,981,219951,81499,animal_model,full/half_sib,no,narrow,authors,non_adult,both,"Fingerling survival (survival between the equalization of families and the start of individual tagging), binary","grow-out survival, binary",survival,survival,include,cor,0.13,0.12,se,NA,NA,NA,NA,NA,NA,rayyan-697471502,table 4,survival,survival,family,0.13073985,1568,1,0.13073985,both,cross,Actinopteri,within
1849,Oncorhynchus mykiss,60,rayyan-697471502,Untangling the positive genetic correlation between rainbow trout growth and survival,2012,1995-2004,Central Finland,field,both,both,1568,1490,NA,NA,852,772,623,678,219951,40406,animal_model,full/half_sib,no,narrow,authors,non_adult,both,"Fingerling survival (survival between the equalization of families and the start of individual tagging), binary",their sea grow-out survival between tagging and the end of the grow-out period in sea,survival,survival,include,cor,0.1,0.16,se,NA,NA,NA,NA,NA,NA,rayyan-697471502,table 4,survival,survival,family,0.100335348,1490,1,0.100335348,both,cross,Actinopteri,within
1850,Oncorhynchus mykiss,60,rayyan-697471502,Untangling the positive genetic correlation between rainbow trout growth and survival,2012,1995-2004,Central Finland,field,both,both,1568,2231,NA,NA,852,1401,623,981,219951,189299,animal_model,full/half_sib,no,narrow,authors,non_adult,non_adult,"Fingerling survival (survival between the equalization of families and the start of individual tagging), binary",weight (fingerlings during tagging),survival,size,include,cor,0.01,0.1,se,NA,NA,NA,NA,NA,NA,rayyan-697471502,table 4,survival,size,family,0.010000333,1568,1,0.010000333,both,non_adult,Actinopteri,between
1851,Oncorhynchus mykiss,60,rayyan-697471502,Untangling the positive genetic correlation between rainbow trout growth and survival,2012,1995-2004,Central Finland,field,both,both,1568,2231,NA,NA,852,1401,623,981,219951,58724,animal_model,full/half_sib,no,narrow,authors,non_adult,adult,"Fingerling survival (survival between the equalization of families and the start of individual tagging), binary",weight during april to june at grow-out period,survival,size,include,cor,-0.14,0.1,se,NA,NA,NA,NA,NA,NA,rayyan-697471502,table 4,survival,size,family,-0.140925576,1568,1,-0.140925576,both,cross,Actinopteri,between
1852,Oncorhynchus mykiss,47,rayyan-697471388,Quantitative genetics of migration-related traits in rainbow and steelhead trout,2015,1996-2004,southeastern Alaska,field,both,both,NA,NA,NA,NA,NA,NA,NA,NA,15008,15008,animal_model,pedigree,no,narrow,authors,non_adult,both,smolt or mature/parr at month 12,weight at month 24,maturation,size,include,cor,0.612,"[0.25, 0.78]",95CI,NA,NA,NA,NA,NA,NA,rayyan-697471388,table s2,maturation,size,pedigree,0.712112792,15008,1,0.712112792,both,cross,Actinopteri,between
1853,Oncorhynchus mykiss,47,rayyan-697471388,Quantitative genetics of migration-related traits in rainbow and steelhead trout,2015,1996-2004,southeastern Alaska,field,both,both,NA,NA,NA,NA,NA,NA,NA,NA,15002,15002,animal_model,pedigree,no,narrow,authors,non_adult,both,smolt or mature/parr at month 12,body condition factor (body length to weight) at month 24,maturation,size,include,cor,-0.97,"[-0.98, -0.94]",95CI,NA,NA,NA,NA,NA,NA,rayyan-697471388,table s2,maturation,size,pedigree,-2.09229572,15002,1,-2.09229572,both,cross,Actinopteri,between
1854,Oncorhynchus mykiss,47,rayyan-697471388,Quantitative genetics of migration-related traits in rainbow and steelhead trout,2015,1996-2004,southeastern Alaska,field,both,both,NA,NA,NA,NA,NA,NA,NA,NA,14955,14955,animal_model,pedigree,no,narrow,authors,non_adult,both,smolt or mature/parr at month 12,Instantaneous growth rate in length from month 15 to 24,maturation,growth,include,cor,0.809,"[0.682, 0.918]",95CI,NA,NA,NA,NA,NA,NA,rayyan-697471388,table s2,maturation,growth,pedigree,1.124128029,14955,1,1.124128029,both,cross,Actinopteri,between
1855,Oncorhynchus mykiss,47,rayyan-697471388,Quantitative genetics of migration-related traits in rainbow and steelhead trout,2015,1996-2004,southeastern Alaska,field,both,both,NA,NA,NA,NA,NA,NA,NA,NA,14940,14940,animal_model,pedigree,no,narrow,authors,non_adult,both,smolt or mature/parr at month 12,Instantaneous growth rate in weightfrom month 15 to 24,maturation,growth,include,cor,0.345,"[0.08, 0.72]",95CI,NA,NA,NA,NA,NA,NA,rayyan-697471388,table s2,maturation,growth,pedigree,0.359757028,14940,1,0.359757028,both,cross,Actinopteri,between
1856,Oncorhynchus mykiss,47,rayyan-697471388,Quantitative genetics of migration-related traits in rainbow and steelhead trout,2015,1996-2004,southeastern Alaska,field,both,both,NA,NA,NA,NA,NA,NA,NA,NA,15565,15565,animal_model,pedigree,no,narrow,authors,both,both,fork length at month 24,Instantaneous growth rate in weightfrom month 15 to 24,size,growth,include,cor,0.489,0.157,se,NA,NA,NA,NA,NA,NA,rayyan-697471388,table s2,size,growth,pedigree,0.534745221,15565,1,0.534745221,both,both,Actinopteri,between
1857,Oncorhynchus mykiss,47,rayyan-697471388,Quantitative genetics of migration-related traits in rainbow and steelhead trout,2015,1996-2004,southeastern Alaska,field,both,both,NA,NA,NA,NA,NA,NA,NA,NA,15621,15621,animal_model,pedigree,no,narrow,authors,non_adult,both,mature or parr/indeterminate/smolt at month 12,fork length at month 12,maturation,size,include,cor,-0.018,"[-0.26, 0.08]",95CI,NA,NA,NA,NA,NA,NA,rayyan-697471388,table s2,maturation,size,pedigree,-0.018001944,15621,1,-0.018001944,both,cross,Actinopteri,between
1858,Oncorhynchus mykiss,47,rayyan-697471388,Quantitative genetics of migration-related traits in rainbow and steelhead trout,2015,1996-2004,southeastern Alaska,field,both,both,NA,NA,NA,NA,NA,NA,NA,NA,15635,15635,animal_model,pedigree,no,narrow,authors,both,both,weight at month 24,body condition factor (body length to weight) at month 24,size,size,include,cor,-0.03,0.147,se,NA,NA,NA,NA,NA,NA,rayyan-697471388,table s2,size,size,pedigree,-0.030009005,15635,1,-0.030009005,both,both,Actinopteri,within
1859,Oncorhynchus mykiss,47,rayyan-697471388,Quantitative genetics of migration-related traits in rainbow and steelhead trout,2015,1996-2004,southeastern Alaska,field,both,both,NA,NA,NA,NA,NA,NA,NA,NA,15581,15581,animal_model,pedigree,no,narrow,authors,both,both,weight at month 24,Instantaneous growth rate in length from month 15 to 24,size,growth,include,cor,0.309,0.173,se,NA,NA,NA,NA,NA,NA,rayyan-697471388,table s2,size,growth,pedigree,0.319439471,15581,1,0.319439471,both,both,Actinopteri,between
1860,Oncorhynchus mykiss,47,rayyan-697471388,Quantitative genetics of migration-related traits in rainbow and steelhead trout,2015,1996-2004,southeastern Alaska,field,both,both,NA,NA,NA,NA,NA,NA,NA,NA,15572,15572,animal_model,pedigree,no,narrow,authors,both,both,weight at month 24,Instantaneous growth rate in weightfrom month 15 to 24,size,growth,include,cor,0.3,0.192,se,NA,NA,NA,NA,NA,NA,rayyan-697471388,table s2,size,growth,pedigree,0.309519604,15572,1,0.309519604,both,both,Actinopteri,between
1861,Oncorhynchus mykiss,47,rayyan-697471388,Quantitative genetics of migration-related traits in rainbow and steelhead trout,2015,1996-2004,southeastern Alaska,field,both,both,NA,NA,NA,NA,NA,NA,NA,NA,1974,1974,animal_model,pedigree,no,narrow,authors,both,both,weight at month 24,measure of overall body at month 24,size,size,include,cor,0.767,0.09,se,NA,NA,NA,NA,NA,NA,rayyan-697471388,table s2,size,size,pedigree,1.013000009,1974,1,1.013000009,both,both,Actinopteri,within
1862,Oncorhynchus mykiss,47,rayyan-697471388,Quantitative genetics of migration-related traits in rainbow and steelhead trout,2015,1996-2004,southeastern Alaska,field,both,both,NA,NA,NA,NA,NA,NA,NA,NA,15581,15581,animal_model,pedigree,no,narrow,authors,both,both,body condition factor (body length to weight) at month 24,Instantaneous growth rate in length from month 15 to 24,size,growth,include,cor,-0.546,0.109,se,NA,NA,NA,NA,NA,NA,rayyan-697471388,table s2,size,growth,pedigree,-0.612664516,15581,1,-0.612664516,both,both,Actinopteri,between
1863,Oncorhynchus mykiss,47,rayyan-697471388,Quantitative genetics of migration-related traits in rainbow and steelhead trout,2015,1996-2004,southeastern Alaska,field,both,both,NA,NA,NA,NA,NA,NA,NA,NA,15565,15565,animal_model,pedigree,no,narrow,authors,both,both,body condition factor (body length to weight) at month 24,Instantaneous growth rate in weightfrom month 15 to 24,size,growth,include,cor,-0.017,0.163,se,NA,NA,NA,NA,NA,NA,rayyan-697471388,table s2,size,growth,pedigree,-0.017001638,15565,1,-0.017001638,both,both,Actinopteri,between
1864,Oncorhynchus mykiss,47,rayyan-697471388,Quantitative genetics of migration-related traits in rainbow and steelhead trout,2015,1996-2004,southeastern Alaska,field,both,both,NA,NA,NA,NA,NA,NA,NA,NA,1974,1974,animal_model,pedigree,no,narrow,authors,both,both,body condition factor (body length to weight) at month 24,measure of overall body at month 24,size,size,include,cor,-0.078,0.184,se,NA,NA,NA,NA,NA,NA,rayyan-697471388,table s2,size,size,pedigree,-0.078158764,1974,1,-0.078158764,both,both,Actinopteri,within
1865,Oncorhynchus mykiss,47,rayyan-697471388,Quantitative genetics of migration-related traits in rainbow and steelhead trout,2015,1996-2004,southeastern Alaska,field,both,both,NA,NA,NA,NA,NA,NA,NA,NA,1961,1961,animal_model,pedigree,no,narrow,authors,both,both,Instantaneous growth rate in weight from month 12 to 15,measure of overall body at month 24,growth,size,include,cor,0.443,0.139,se,NA,NA,NA,NA,NA,NA,rayyan-697471388,table s2,growth,size,pedigree,0.475957159,1961,1,0.475957159,both,both,Actinopteri,between
1866,Oncorhynchus mykiss,60,rayyan-697471502,Untangling the positive genetic correlation between rainbow trout growth and survival,2012,1995-2004,Central Finland,field,both,both,1568,1959,NA,NA,852,1129,623,889,219951,41678,animal_model,full/half_sib,no,narrow,authors,non_adult,adult,"Fingerling survival (survival between the equalization of families and the start of individual tagging), binary",weight during oct to april at sea grow-out period,survival,size,include,cor,0.03,0.11,se,NA,NA,NA,NA,NA,NA,rayyan-697471502,table 4,survival,size,family,0.030009005,1568,1,0.030009005,both,cross,Actinopteri,between
1867,Oncorhynchus mykiss,47,rayyan-697471388,Quantitative genetics of migration-related traits in rainbow and steelhead trout,2015,1996-2004,southeastern Alaska,field,both,both,NA,NA,NA,NA,NA,NA,NA,NA,15635,15635,animal_model,pedigree,no,narrow,authors,both,both,fork length at month 24,body condition factor (body length to weight) at month 24,size,size,include,cor,-0.341,0.12,se,NA,NA,NA,NA,NA,NA,rayyan-697471388,table s2,size,size,pedigree,-0.355223674,15635,1,-0.355223674,both,both,Actinopteri,within
1868,Oncorhynchus mykiss,47,rayyan-697471388,Quantitative genetics of migration-related traits in rainbow and steelhead trout,2015,1996-2004,southeastern Alaska,field,both,both,NA,NA,NA,NA,NA,NA,NA,NA,15588,15588,animal_model,pedigree,no,narrow,authors,both,both,fork length at month 24,Instantaneous growth rate in length from month 15 to 24,size,growth,include,cor,0.563,0.124,se,NA,NA,NA,NA,NA,NA,rayyan-697471388,table s2,size,growth,pedigree,0.637214568,15588,1,0.637214568,both,both,Actinopteri,between
1869,Oncorhynchus mykiss,47,rayyan-697471388,Quantitative genetics of migration-related traits in rainbow and steelhead trout,2015,1996-2004,southeastern Alaska,field,both,both,NA,NA,NA,NA,NA,NA,NA,NA,15022,15022,animal_model,pedigree,no,narrow,authors,non_adult,non_adult,smolt or mature/parr at month 12,mature or parr/indeterminate/smolt at month 12,maturation,maturation,include,cor,-0.99,"[-0.999, -0.98]",95CI,NA,NA,NA,NA,NA,NA,rayyan-697471388,table s2,maturation,maturation,pedigree,-2.646652412,15022,1,-2.646652412,both,non_adult,Actinopteri,within
1870,Oncorhynchus mykiss,47,rayyan-697471388,Quantitative genetics of migration-related traits in rainbow and steelhead trout,2015,1996-2004,southeastern Alaska,field,both,both,NA,NA,NA,NA,NA,NA,NA,NA,1974,1974,animal_model,pedigree,no,narrow,authors,both,both,fork length at month 24,measure of overall body at month 24,size,size,include,cor,0.777,0.085,se,NA,NA,NA,NA,NA,NA,rayyan-697471388,table s2,size,size,pedigree,1.037755028,1974,1,1.037755028,both,both,Actinopteri,within
1871,Oncorhynchus mykiss,47,rayyan-697471388,Quantitative genetics of migration-related traits in rainbow and steelhead trout,2015,1996-2004,southeastern Alaska,field,both,both,NA,NA,NA,NA,NA,NA,NA,NA,14972,14972,animal_model,pedigree,no,narrow,authors,non_adult,both,smolt or mature/parr at month 12,weight at month 12,maturation,size,include,cor,0.25,"[-0.31, 0.40]",95CI,NA,NA,NA,NA,NA,NA,rayyan-697471388,table s2,maturation,size,pedigree,0.255412812,14972,1,0.255412812,both,cross,Actinopteri,between
1872,Oncorhynchus mykiss,294,rayyan-197247867,Genetic architecture of growth and early life-history transitions in anadromous and derived freshwater populations of steelhead,2004,1996-1998,"Sashin Lake, Alaska, USA",lab,both,both,75,75,NA,NA,41,41,31,31,6593,6593,animal_model,full/half_sib,no,narrow,authors,non_adult,non_adult,proportion smolting at age 2 years,proportion maturing at age 2 years,maturation,maturation,include,cor,-0.441,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-197247867,table 3,maturation,maturation,family,-0.473471561,75,1,-0.473471561,both,non_adult,Actinopteri,within
1873,Oncorhynchus mykiss,47,rayyan-697471388,Quantitative genetics of migration-related traits in rainbow and steelhead trout,2015,1996-2004,southeastern Alaska,field,both,both,NA,NA,NA,NA,NA,NA,NA,NA,15685,15685,animal_model,pedigree,no,narrow,authors,both,both,body condition factor (body length to weight) at month 15,Instantaneous growth rate in length from month 12 to 15,size,growth,include,cor,0.09,0.14,se,NA,NA,NA,NA,NA,NA,rayyan-697471388,table s2,size,growth,pedigree,0.090244188,15685,1,0.090244188,both,both,Actinopteri,between
1874,Oncorhynchus mykiss,47,rayyan-697471388,Quantitative genetics of migration-related traits in rainbow and steelhead trout,2015,1996-2004,southeastern Alaska,field,both,both,NA,NA,NA,NA,NA,NA,NA,NA,15639,15639,animal_model,pedigree,no,narrow,authors,both,both,body condition factor (body length to weight) at month 15,Instantaneous growth rate in weight from month 12 to 15,size,growth,include,cor,0.246,0.134,se,NA,NA,NA,NA,NA,NA,rayyan-697471388,table s2,size,growth,pedigree,0.251150666,15639,1,0.251150666,both,both,Actinopteri,between
1875,Oncorhynchus mykiss,47,rayyan-697471388,Quantitative genetics of migration-related traits in rainbow and steelhead trout,2015,1996-2004,southeastern Alaska,field,both,both,NA,NA,NA,NA,NA,NA,NA,NA,14943,14943,animal_model,pedigree,no,narrow,authors,non_adult,both,smolt or mature/parr at month 12,body condition factor (body length to weight) at month 15,maturation,size,include,cor,-0.64,"[-0.89, -0.48]",95CI,NA,NA,NA,NA,NA,NA,rayyan-697471388,table s2,maturation,size,pedigree,-0.758173745,14943,1,-0.758173745,both,cross,Actinopteri,between
1876,Oncorhynchus mykiss,47,rayyan-697471388,Quantitative genetics of migration-related traits in rainbow and steelhead trout,2015,1996-2004,southeastern Alaska,field,both,both,NA,NA,NA,NA,NA,NA,NA,NA,14961,14961,animal_model,pedigree,no,narrow,authors,non_adult,both,smolt or mature/parr at month 12,Instantaneous growth rate in length from month 12 to 15,maturation,growth,include,cor,0.297,"[0.08, 0.58]",95CI,NA,NA,NA,NA,NA,NA,rayyan-697471388,table s2,maturation,growth,pedigree,0.306226146,14961,1,0.306226146,both,cross,Actinopteri,between
1877,Oncorhynchus mykiss,47,rayyan-697471388,Quantitative genetics of migration-related traits in rainbow and steelhead trout,2015,1996-2004,southeastern Alaska,field,both,both,NA,NA,NA,NA,NA,NA,NA,NA,14904,14904,animal_model,pedigree,no,narrow,authors,non_adult,both,smolt or mature/parr at month 12,Instantaneous growth rate in weight from month 12 to 15,maturation,growth,include,cor,0.241,"[-0.04, 0.46]",95CI,NA,NA,NA,NA,NA,NA,rayyan-697471388,table s2,maturation,growth,pedigree,0.245835504,14904,1,0.245835504,both,cross,Actinopteri,between
1878,Oncorhynchus mykiss,47,rayyan-697471388,Quantitative genetics of migration-related traits in rainbow and steelhead trout,2015,1996-2004,southeastern Alaska,field,both,both,NA,NA,NA,NA,NA,NA,NA,NA,15562,15562,animal_model,pedigree,no,narrow,authors,both,both,body condition factor (body length to weight) at month 15,Instantaneous growth rate in length from month 15 to 24,size,growth,include,cor,-0.26,0.15,se,NA,NA,NA,NA,NA,NA,rayyan-697471388,table s2,size,growth,pedigree,-0.266108407,15562,1,-0.266108407,both,both,Actinopteri,between
1879,Oncorhynchus mykiss,47,rayyan-697471388,Quantitative genetics of migration-related traits in rainbow and steelhead trout,2015,1996-2004,southeastern Alaska,field,both,both,NA,NA,NA,NA,NA,NA,NA,NA,15562,15562,animal_model,pedigree,no,narrow,authors,both,both,body condition factor (body length to weight) at month 15,Instantaneous growth rate in weightfrom month 15 to 24,size,growth,include,cor,-0.269,0.167,se,NA,NA,NA,NA,NA,NA,rayyan-697471388,table s2,size,growth,pedigree,-0.275785504,15562,1,-0.275785504,both,both,Actinopteri,between
1880,Oncorhynchus mykiss,47,rayyan-697471388,Quantitative genetics of migration-related traits in rainbow and steelhead trout,2015,1996-2004,southeastern Alaska,field,both,both,NA,NA,NA,NA,NA,NA,NA,NA,1972,1972,animal_model,pedigree,no,narrow,authors,both,both,body condition factor (body length to weight) at month 15,measure of overall body at month 24,size,size,include,cor,-0.032,0.171,se,NA,NA,NA,NA,NA,NA,rayyan-697471388,table s2,size,size,pedigree,-0.032010929,1972,1,-0.032010929,both,both,Actinopteri,within
1881,Oncorhynchus mykiss,60,rayyan-697471502,Untangling the positive genetic correlation between rainbow trout growth and survival,2012,1995-2004,Central Finland,field,both,both,1490,1959,NA,NA,772,1129,678,889,40406,41678,animal_model,full/half_sib,no,narrow,authors,both,adult,"their sea grow-out survival between tagging and the end of the grow-out period in sea, binary",weight during oct to april at sea grow-out period,survival,size,include,cor,0.4,0.08,se,NA,NA,NA,NA,NA,NA,rayyan-697471502,table 4,survival,size,family,0.42364893,1490,1,0.42364893,both,cross,Actinopteri,between
1882,Oncorhynchus mykiss,47,rayyan-697471388,Quantitative genetics of migration-related traits in rainbow and steelhead trout,2015,1996-2004,southeastern Alaska,field,both,both,NA,NA,NA,NA,NA,NA,NA,NA,15576,15576,animal_model,pedigree,no,narrow,authors,both,both,Instantaneous growth rate in length from month 12 to 15,fork length at month 24,growth,size,include,cor,0.682,0.122,se,NA,NA,NA,NA,NA,NA,rayyan-697471388,table s2,growth,size,pedigree,0.832843729,15576,1,0.832843729,both,both,Actinopteri,between
1883,Oncorhynchus mykiss,47,rayyan-697471388,Quantitative genetics of migration-related traits in rainbow and steelhead trout,2015,1996-2004,southeastern Alaska,field,both,both,NA,NA,NA,NA,NA,NA,NA,NA,15576,15576,animal_model,pedigree,no,narrow,authors,both,both,Instantaneous growth rate in length from month 12 to 15,weight at month 24,growth,size,include,cor,0.731,0.126,se,NA,NA,NA,NA,NA,NA,rayyan-697471388,table s2,growth,size,pedigree,0.930871588,15576,1,0.930871588,both,both,Actinopteri,between
1884,Oncorhynchus mykiss,47,rayyan-697471388,Quantitative genetics of migration-related traits in rainbow and steelhead trout,2015,1996-2004,southeastern Alaska,field,both,both,NA,NA,NA,NA,NA,NA,NA,NA,15569,15569,animal_model,pedigree,no,narrow,authors,both,both,Instantaneous growth rate in length from month 12 to 15,body condition factor (body length to weight) at month 24,growth,size,include,cor,-0.082,0.123,se,NA,NA,NA,NA,NA,NA,rayyan-697471388,table s2,growth,size,pedigree,-0.082184534,15569,1,-0.082184534,both,both,Actinopteri,between
1885,Oncorhynchus mykiss,47,rayyan-697471388,Quantitative genetics of migration-related traits in rainbow and steelhead trout,2015,1996-2004,southeastern Alaska,field,both,both,NA,NA,NA,NA,NA,NA,NA,NA,15576,15576,animal_model,pedigree,no,narrow,authors,both,both,Instantaneous growth rate in length from month 12 to 15,Instantaneous growth rate in length from month 15 to 24,growth,growth,include,cor,0.406,0.148,se,NA,NA,NA,NA,NA,NA,rayyan-697471388,table s2,growth,growth,pedigree,0.430812377,15576,1,0.430812377,both,both,Actinopteri,within
1886,Oncorhynchus mykiss,47,rayyan-697471388,Quantitative genetics of migration-related traits in rainbow and steelhead trout,2015,1996-2004,southeastern Alaska,field,both,both,NA,NA,NA,NA,NA,NA,NA,NA,15550,15550,animal_model,pedigree,no,narrow,authors,both,both,Instantaneous growth rate in length from month 12 to 15,Instantaneous growth rate in weightfrom month 15 to 24,growth,growth,include,cor,0.335,0.173,se,NA,NA,NA,NA,NA,NA,rayyan-697471388,table s2,growth,growth,pedigree,0.348449765,15550,1,0.348449765,both,both,Actinopteri,within
1887,Oncorhynchus mykiss,47,rayyan-697471388,Quantitative genetics of migration-related traits in rainbow and steelhead trout,2015,1996-2004,southeastern Alaska,field,both,both,NA,NA,NA,NA,NA,NA,NA,NA,1971,1971,animal_model,pedigree,no,narrow,authors,both,both,Instantaneous growth rate in length from month 12 to 15,measure of overall body at month 24,growth,size,include,cor,0.441,0.133,se,NA,NA,NA,NA,NA,NA,rayyan-697471388,table s2,growth,size,pedigree,0.473471561,1971,1,0.473471561,both,both,Actinopteri,between
1888,Oncorhynchus mykiss,294,rayyan-197247867,Genetic architecture of growth and early life-history transitions in anadromous and derived freshwater populations of steelhead,2004,1996-1998,"Sashin Lake, Alaska, USA",lab,both,both,75,75,NA,NA,41,41,31,31,6573,6570,animal_model,full/half_sib,no,narrow,authors,both,both,mass in october 1997  (age 1),daily growth in mass between june and october 1997 (age 1),size,growth,include,cor,0.426,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-197247867,table 3,size,growth,family,0.454999602,75,1,0.454999602,both,both,Actinopteri,between
1889,Oncorhynchus mykiss,294,rayyan-197247867,Genetic architecture of growth and early life-history transitions in anadromous and derived freshwater populations of steelhead,2004,1996-1998,"Sashin Lake, Alaska, USA",lab,both,both,75,75,NA,NA,41,41,31,31,6573,6565,animal_model,full/half_sib,no,narrow,authors,both,both,mass in october 1997  (age 1),daily growth in mass between october 1997 and june 1998 (age 1-2),size,growth,include,cor,-0.219,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-197247867,table 3,size,growth,family,-0.22260549,75,1,-0.22260549,both,both,Actinopteri,between
1890,Oncorhynchus mykiss,294,rayyan-197247867,Genetic architecture of growth and early life-history transitions in anadromous and derived freshwater populations of steelhead,2004,1996-1998,"Sashin Lake, Alaska, USA",lab,both,both,75,75,NA,NA,41,41,31,31,6582,6570,animal_model,full/half_sib,no,narrow,authors,both,both,mass in june 1998  (age 2),daily growth in mass between june and october 1997 (age 1),size,growth,include,cor,0.628,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-197247867,table 3,size,growth,family,0.738106846,75,1,0.738106846,both,both,Actinopteri,between
1891,Oncorhynchus mykiss,294,rayyan-197247867,Genetic architecture of growth and early life-history transitions in anadromous and derived freshwater populations of steelhead,2004,1996-1998,"Sashin Lake, Alaska, USA",lab,both,both,75,75,NA,NA,41,41,31,31,6582,6565,animal_model,full/half_sib,no,narrow,authors,both,both,mass in june 1998  (age 2),daily growth in mass between october 1997 and june 1998 (age 1-2),size,growth,include,cor,-0.083,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-197247867,table 3,size,growth,family,-0.083191387,75,1,-0.083191387,both,both,Actinopteri,between
1892,Oncorhynchus mykiss,60,rayyan-697471502,Untangling the positive genetic correlation between rainbow trout growth and survival,2012,1995-2004,Central Finland,field,both,both,1568,2231,NA,NA,852,1401,623,981,219951,45242,animal_model,full/half_sib,no,narrow,authors,non_adult,adult,"Fingerling survival (survival between the equalization of families and the start of individual tagging), binary",weight at 3 year old,survival,size,include,cor,-0.14,0.1,se,NA,NA,NA,NA,NA,NA,rayyan-697471502,table 4,survival,size,family,-0.140925576,1568,1,-0.140925576,both,cross,Actinopteri,between
1893,Oncorhynchus mykiss,294,rayyan-197247867,Genetic architecture of growth and early life-history transitions in anadromous and derived freshwater populations of steelhead,2004,1996-1998,"Sashin Lake, Alaska, USA",lab,both,both,75,75,NA,NA,41,41,31,31,6593,6593,animal_model,full/half_sib,no,narrow,authors,non_adult,non_adult,proportion maturing at age 2 years,proportion smolting at age 2 years,maturation,maturation,include,cor,-0.841,"[-2.7, 4.872]",95CI,NA,NA,NA,NA,NA,NA,rayyan-197247867,table 4,maturation,maturation,family,-1.22457999,75,1,-1.22457999,both,non_adult,Actinopteri,within
1894,Oncorhynchus mykiss,47,rayyan-697471388,Quantitative genetics of migration-related traits in rainbow and steelhead trout,2015,1996-2004,southeastern Alaska,field,both,both,NA,NA,NA,NA,NA,NA,NA,NA,15632,15632,animal_model,pedigree,no,narrow,authors,both,both,Instantaneous growth rate in length from month 12 to 15,Instantaneous growth rate in weight from month 12 to 15,growth,growth,include,cor,0.945,0.009,se,NA,NA,NA,NA,NA,NA,rayyan-697471388,table s2,growth,growth,pedigree,1.782842035,15632,1,1.782842035,both,both,Actinopteri,within
1895,Oncorhynchus mykiss,60,rayyan-697471502,Untangling the positive genetic correlation between rainbow trout growth and survival,2012,1995-2004,Central Finland,field,both,male,1568,2231,NA,NA,852,1146,623,981,219951,21992,animal_model,full/half_sib,no,narrow,authors,non_adult,non_adult,"Fingerling survival (survival between the equalization of families and the start of individual tagging), binary","male maturity after both 2 and 3 growthing seasons, binary",survival,maturation,include,cor,-0.07,0.06,se,NA,NA,NA,NA,NA,NA,rayyan-697471502,table 4,survival,maturation,family,-0.070114671,1568,1,-0.070114671,male,non_adult,Actinopteri,between
1896,Oncorhynchus mykiss,60,rayyan-697471502,Untangling the positive genetic correlation between rainbow trout growth and survival,2012,1995-2004,Central Finland,field,both,male,1568,1959,NA,NA,852,1129,623,889,219951,17938,animal_model,full/half_sib,no,narrow,authors,non_adult,non_adult,"Fingerling survival (survival between the equalization of families and the start of individual tagging), binary","male maturity after both 2 and 3 growthing seasons at sea, binary",survival,maturation,include,cor,-0.12,0.12,se,NA,NA,NA,NA,NA,NA,rayyan-697471502,table 4,survival,maturation,family,-0.120581028,1568,1,-0.120581028,male,non_adult,Actinopteri,between
1897,Oncorhynchus mykiss,60,rayyan-697471502,Untangling the positive genetic correlation between rainbow trout growth and survival,2012,1995-2004,Central Finland,field,both,both,2231,1490,NA,NA,1401,772,981,678,81499,40406,animal_model,full/half_sib,no,narrow,authors,both,both,"grow-out survival, binary","their sea grow-out survival between tagging and the end of the grow-out period in sea, binary",survival,survival,include,cor,0.56,0.09,se,NA,NA,NA,NA,NA,NA,rayyan-697471502,table 4,survival,survival,family,0.632833187,1490,1,0.632833187,both,both,Actinopteri,within
1898,Oncorhynchus mykiss,60,rayyan-697471502,Untangling the positive genetic correlation between rainbow trout growth and survival,2012,1995-2004,Central Finland,field,both,both,2231,2231,NA,NA,1401,1401,981,981,81499,189299,animal_model,full/half_sib,no,narrow,authors,both,non_adult,"grow-out survival, binary",weight (fingerlings during tagging),survival,size,include,cor,0.1,0.07,se,NA,NA,NA,NA,NA,NA,rayyan-697471502,table 4,survival,size,family,0.100335348,2231,1,0.100335348,both,cross,Actinopteri,between
1899,Oncorhynchus mykiss,60,rayyan-697471502,Untangling the positive genetic correlation between rainbow trout growth and survival,2012,1995-2004,Central Finland,field,both,both,2231,2231,NA,NA,1401,1401,981,981,81499,58724,animal_model,full/half_sib,no,narrow,authors,both,adult,"grow-out survival, binary",weight during april to june at grow-out period,survival,size,include,cor,0.16,0.04,se,NA,NA,NA,NA,NA,NA,rayyan-697471502,table 4,survival,size,family,0.161386696,2231,1,0.161386696,both,cross,Actinopteri,between
1900,Oncorhynchus mykiss,60,rayyan-697471502,Untangling the positive genetic correlation between rainbow trout growth and survival,2012,1995-2004,Central Finland,field,both,both,2231,2231,NA,NA,1401,1401,981,981,81499,45242,animal_model,full/half_sib,no,narrow,authors,both,adult,"grow-out survival, binary",weight at 3 year old,survival,size,include,cor,0.21,0.04,se,NA,NA,NA,NA,NA,NA,rayyan-697471502,table 4,survival,size,family,0.213171347,2231,1,0.213171347,both,cross,Actinopteri,between
1901,Oncorhynchus mykiss,60,rayyan-697471502,Untangling the positive genetic correlation between rainbow trout growth and survival,2012,1995-2004,Central Finland,field,both,both,2231,1959,NA,NA,1401,1129,981,889,81499,41678,animal_model,full/half_sib,no,narrow,authors,both,adult,"grow-out survival, binary",weight during oct to april at sea grow-out period,survival,size,include,cor,0.23,0.07,se,NA,NA,NA,NA,NA,NA,rayyan-697471502,table 4,survival,size,family,0.234189467,1959,1,0.234189467,both,cross,Actinopteri,between
1902,Oncorhynchus mykiss,60,rayyan-697471502,Untangling the positive genetic correlation between rainbow trout growth and survival,2012,1995-2004,Central Finland,field,both,female,2231,1809,NA,NA,1401,979,981,814,81499,20263,animal_model,full/half_sib,no,narrow,authors,both,non_adult,"grow-out survival, binary","female maturity after both 2 and 3 growthing seasons, binary",survival,maturation,include,cor,0.06,0.07,se,NA,NA,NA,NA,NA,NA,rayyan-697471502,table 4,survival,maturation,family,0.060072156,1809,1,0.060072156,female,cross,Actinopteri,between
1903,Oncorhynchus mykiss,60,rayyan-697471502,Untangling the positive genetic correlation between rainbow trout growth and survival,2012,1995-2004,Central Finland,field,both,male,2231,2231,NA,NA,1401,1146,981,981,81499,21992,animal_model,full/half_sib,no,narrow,authors,both,non_adult,"grow-out survival, binary","male maturity after both 2 and 3 growthing seasons, binary",survival,maturation,include,cor,0.08,0.08,se,NA,NA,NA,NA,NA,NA,rayyan-697471502,table 4,survival,maturation,family,0.080171325,2231,1,0.080171325,male,cross,Actinopteri,between
1904,Oncorhynchus mykiss,60,rayyan-697471502,Untangling the positive genetic correlation between rainbow trout growth and survival,2012,1995-2004,Central Finland,field,both,male,2231,1959,NA,NA,1401,1129,981,889,81499,17938,animal_model,full/half_sib,no,narrow,authors,both,non_adult,"grow-out survival, binary","male maturity after both 2 and 3 growthing seasons at sea, binary",survival,maturation,include,cor,0.04,0.09,se,NA,NA,NA,NA,NA,NA,rayyan-697471502,table 4,survival,maturation,family,0.040021354,1959,1,0.040021354,male,cross,Actinopteri,between
1905,Oncorhynchus mykiss,47,rayyan-697471388,Quantitative genetics of migration-related traits in rainbow and steelhead trout,2015,1996-2004,southeastern Alaska,field,both,both,NA,NA,NA,NA,NA,NA,NA,NA,15555,15555,animal_model,pedigree,no,narrow,authors,both,both,Instantaneous growth rate in length from month 15 to 24,Instantaneous growth rate in weightfrom month 15 to 24,growth,growth,include,cor,0.862,0.048,se,NA,NA,NA,NA,NA,NA,rayyan-697471388,table s2,growth,growth,pedigree,1.301076386,15555,1,1.301076386,both,both,Actinopteri,within
1906,Oncorhynchus mykiss,47,rayyan-697471388,Quantitative genetics of migration-related traits in rainbow and steelhead trout,2015,1996-2004,southeastern Alaska,field,both,both,NA,NA,NA,NA,NA,NA,NA,NA,1970,1970,animal_model,pedigree,no,narrow,authors,both,both,Instantaneous growth rate in length from month 15 to 24,measure of overall body at month 24,growth,size,include,cor,0.738,0.087,se,NA,NA,NA,NA,NA,NA,rayyan-697471388,table s2,growth,size,pedigree,0.946072901,1970,1,0.946072901,both,both,Actinopteri,between
1907,Oncorhynchus mykiss,60,rayyan-697471502,Untangling the positive genetic correlation between rainbow trout growth and survival,2012,1995-2004,Central Finland,field,both,female,1568,1809,NA,NA,852,979,623,814,219951,20263,animal_model,full/half_sib,no,narrow,authors,non_adult,non_adult,"Fingerling survival (survival between the equalization of families and the start of individual tagging), binary","female maturity after both 2 and 3 growthing seasons, binary",survival,maturation,include,cor,0.07,0.11,se,NA,NA,NA,NA,NA,NA,rayyan-697471502,table 4,survival,maturation,family,0.070114671,1568,1,0.070114671,female,non_adult,Actinopteri,between
1908,Oncorhynchus mykiss,60,rayyan-697471502,Untangling the positive genetic correlation between rainbow trout growth and survival,2012,1995-2004,Central Finland,field,both,both,1490,2231,NA,NA,772,1401,678,981,40406,45242,animal_model,full/half_sib,no,narrow,authors,both,adult,"their sea grow-out survival between tagging and the end of the grow-out period in sea, binary",weight at 3 year old,survival,size,include,cor,0.07,0.09,se,NA,NA,NA,NA,NA,NA,rayyan-697471502,table 4,survival,size,family,0.070114671,1490,1,0.070114671,both,cross,Actinopteri,between
1909,Oncorhynchus mykiss,60,rayyan-697471502,Untangling the positive genetic correlation between rainbow trout growth and survival,2012,1995-2004,Central Finland,field,both,female,1490,1809,NA,NA,772,979,678,814,40406,20263,animal_model,full/half_sib,no,narrow,authors,both,non_adult,"their sea grow-out survival between tagging and the end of the grow-out period in sea, binary","female maturity after both 2 and 3 growthing seasons, binary",survival,maturation,include,cor,-0.05,0.1,se,NA,NA,NA,NA,NA,NA,rayyan-697471502,table 4,survival,maturation,family,-0.050041729,1490,1,-0.050041729,female,cross,Actinopteri,between
1910,Oncorhynchus mykiss,47,rayyan-697471388,Quantitative genetics of migration-related traits in rainbow and steelhead trout,2015,1996-2004,southeastern Alaska,field,both,both,NA,NA,NA,NA,NA,NA,NA,NA,15014,15014,animal_model,pedigree,no,narrow,authors,non_adult,both,smolt or mature/parr at month 12,fork length at month 12,maturation,size,include,cor,0.69,"[0.64, 0.87]",95CI,NA,NA,NA,NA,NA,NA,rayyan-697471388,table s2,maturation,size,pedigree,0.847955755,15014,1,0.847955755,both,cross,Actinopteri,between
1911,Oncorhynchus mykiss,60,rayyan-697471502,Untangling the positive genetic correlation between rainbow trout growth and survival,2012,1995-2004,Central Finland,field,both,male,1490,1959,NA,NA,772,1129,678,889,40406,17938,animal_model,full/half_sib,no,narrow,authors,both,non_adult,"their sea grow-out survival between tagging and the end of the grow-out period in sea, binary","male maturity after both 2 and 3 growthing seasons at sea, binary",survival,maturation,include,cor,0.24,0.11,se,NA,NA,NA,NA,NA,NA,rayyan-697471502,table 4,survival,maturation,family,0.244774113,1490,1,0.244774113,male,cross,Actinopteri,between
1912,Oncorhynchus mykiss,60,rayyan-697471502,Untangling the positive genetic correlation between rainbow trout growth and survival,2012,1995-2004,Central Finland,field,both,male,2231,2231,NA,NA,1401,1146,981,981,189299,21992,animal_model,full/half_sib,no,narrow,authors,non_adult,non_adult,weight (fingerlings during tagging),"male maturity after both 2 and 3 growthing seasons, binary",size,maturation,include,cor,0.01,0.06,se,NA,NA,NA,NA,NA,NA,rayyan-697471502,appendix 2,size,maturation,family,0.010000333,2231,1,0.010000333,male,non_adult,Actinopteri,between
1913,Oncorhynchus mykiss,60,rayyan-697471502,Untangling the positive genetic correlation between rainbow trout growth and survival,2012,1995-2004,Central Finland,field,both,male,2231,1959,NA,NA,1401,1129,981,889,189299,17938,animal_model,full/half_sib,no,narrow,authors,non_adult,non_adult,weight (fingerlings during tagging),"male maturity after both 2 and 3 growthing seasons at sea, binary",size,maturation,include,cor,0.06,0.07,se,NA,NA,NA,NA,NA,NA,rayyan-697471502,appendix 2,size,maturation,family,0.060072156,1959,1,0.060072156,male,non_adult,Actinopteri,between
1914,Oncorhynchus mykiss,60,rayyan-697471502,Untangling the positive genetic correlation between rainbow trout growth and survival,2012,1995-2004,Central Finland,field,both,both,2231,2231,NA,NA,1401,1401,981,981,58724,45242,animal_model,full/half_sib,no,narrow,authors,adult,adult,weight during april to june at grow-out period,weight at 3 year old,size,size,include,cor,0.88,0.01,se,NA,NA,NA,NA,NA,NA,rayyan-697471502,appendix 2,size,size,family,1.375767657,2231,1,1.375767657,both,adult,Actinopteri,within
1915,Oncorhynchus mykiss,60,rayyan-697471502,Untangling the positive genetic correlation between rainbow trout growth and survival,2012,1995-2004,Central Finland,field,both,both,2231,1959,NA,NA,1401,1129,981,889,58724,41678,animal_model,full/half_sib,no,narrow,authors,adult,adult,weight during april to june at grow-out period,weight during oct to april at sea grow-out period,size,size,include,cor,0.58,0.04,se,NA,NA,NA,NA,NA,NA,rayyan-697471502,appendix 2,size,size,family,0.662462707,1959,1,0.662462707,both,adult,Actinopteri,within
1916,Oncorhynchus mykiss,47,rayyan-697471388,Quantitative genetics of migration-related traits in rainbow and steelhead trout,2015,1996-2004,southeastern Alaska,field,both,both,NA,NA,NA,NA,NA,NA,NA,NA,15562,15562,animal_model,pedigree,no,narrow,authors,both,both,body condition factor (body length to weight) at month 15,weight at month 24,size,size,include,cor,0.082,0.158,se,NA,NA,NA,NA,NA,NA,rayyan-697471388,table s2,size,size,pedigree,0.082184534,15562,1,0.082184534,both,both,Actinopteri,within
1917,Oncorhynchus mykiss,47,rayyan-697471388,Quantitative genetics of migration-related traits in rainbow and steelhead trout,2015,1996-2004,southeastern Alaska,field,both,both,NA,NA,NA,NA,NA,NA,NA,NA,15555,15555,animal_model,pedigree,no,narrow,authors,both,both,body condition factor (body length to weight) at month 15,body condition factor (body length to weight) at month 24,size,size,include,cor,0.777,0.055,se,NA,NA,NA,NA,NA,NA,rayyan-697471388,table s2,size,size,pedigree,1.037755028,15555,1,1.037755028,both,both,Actinopteri,within
1918,Oncorhynchus mykiss,60,rayyan-697471502,Untangling the positive genetic correlation between rainbow trout growth and survival,2012,1995-2004,Central Finland,field,both,male,2231,1959,NA,NA,1401,1054,981,889,58724,17938,animal_model,full/half_sib,no,narrow,authors,adult,non_adult,weight during april to june at grow-out period,"male maturity after both 2 and 3 growthing seasons at sea, binary",size,maturation,include,cor,0.13,0.07,se,NA,NA,NA,NA,NA,NA,rayyan-697471502,appendix 2,size,maturation,family,0.13073985,1959,1,0.13073985,male,cross,Actinopteri,between
1919,Oncorhynchus mykiss,60,rayyan-697471502,Untangling the positive genetic correlation between rainbow trout growth and survival,2012,1995-2004,Central Finland,field,both,both,2231,1959,NA,NA,1401,1129,981,889,45242,41678,animal_model,full/half_sib,no,narrow,authors,adult,adult,weight at 3 year old,weight during oct to april at sea grow-out period,size,size,include,cor,0.48,0.05,se,NA,NA,NA,NA,NA,NA,rayyan-697471502,appendix 2,size,size,family,0.522984278,1959,1,0.522984278,both,adult,Actinopteri,within
1920,Oncorhynchus mykiss,60,rayyan-697471502,Untangling the positive genetic correlation between rainbow trout growth and survival,2012,1995-2004,Central Finland,field,both,female,2231,1809,NA,NA,1401,979,981,814,45242,20263,animal_model,full/half_sib,no,narrow,authors,adult,non_adult,weight at 3 year old,"female maturity after both 2 and 3 growthing seasons, binary",size,maturation,include,cor,0.51,0.05,se,NA,NA,NA,NA,NA,NA,rayyan-697471502,appendix 2,size,maturation,family,0.562729769,1809,1,0.562729769,female,cross,Actinopteri,between
1921,Oncorhynchus mykiss,60,rayyan-697471502,Untangling the positive genetic correlation between rainbow trout growth and survival,2012,1995-2004,Central Finland,field,both,male,2231,2231,NA,NA,1401,1146,981,981,45242,21992,animal_model,full/half_sib,no,narrow,authors,adult,non_adult,weight at 3 year old,"male maturity after both 2 and 3 growthing seasons, binary",size,maturation,include,cor,0.08,0.05,se,NA,NA,NA,NA,NA,NA,rayyan-697471502,appendix 2,size,maturation,family,0.080171325,2231,1,0.080171325,male,cross,Actinopteri,between
1922,Oncorhynchus mykiss,60,rayyan-697471502,Untangling the positive genetic correlation between rainbow trout growth and survival,2012,1995-2004,Central Finland,field,both,male,2231,1959,NA,NA,1401,1129,981,889,45242,17938,animal_model,full/half_sib,no,narrow,authors,adult,non_adult,weight at 3 year old,"male maturity after both 2 and 3 growthing seasons at sea, binary",size,maturation,include,cor,0.13,0.07,se,NA,NA,NA,NA,NA,NA,rayyan-697471502,appendix 2,size,maturation,family,0.13073985,1959,1,0.13073985,male,cross,Actinopteri,between
1923,Oncorhynchus mykiss,60,rayyan-697471502,Untangling the positive genetic correlation between rainbow trout growth and survival,2012,1995-2004,Central Finland,field,both,female,1959,1809,NA,NA,1129,979,889,814,41678,20263,animal_model,full/half_sib,no,narrow,authors,adult,non_adult,weight during oct to april at sea grow-out period,"female maturity after both 2 and 3 growthing seasons, binary",size,maturation,include,cor,0.2,0.06,se,NA,NA,NA,NA,NA,NA,rayyan-697471502,appendix 2,size,maturation,family,0.202732554,1809,1,0.202732554,female,cross,Actinopteri,between
1924,Oncorhynchus mykiss,60,rayyan-697471502,Untangling the positive genetic correlation between rainbow trout growth and survival,2012,1995-2004,Central Finland,field,both,male,1959,2231,NA,NA,1129,1146,889,981,41678,21992,animal_model,full/half_sib,no,narrow,authors,adult,non_adult,weight during oct to april at sea grow-out period,"male maturity after both 2 and 3 growthing seasons, binary",size,maturation,include,cor,0.11,0.06,se,NA,NA,NA,NA,NA,NA,rayyan-697471502,appendix 2,size,maturation,family,0.110446916,1959,1,0.110446916,male,cross,Actinopteri,between
1925,Oncorhynchus mykiss,60,rayyan-697471502,Untangling the positive genetic correlation between rainbow trout growth and survival,2012,1995-2004,Central Finland,field,both,male,1959,1959,NA,NA,1129,1129,889,889,41678,17938,animal_model,full/half_sib,no,narrow,authors,adult,non_adult,weight during oct to april at sea grow-out period,"male maturity after both 2 and 3 growthing seasons at sea, binary",size,maturation,include,cor,0.12,0.07,se,NA,NA,NA,NA,NA,NA,rayyan-697471502,appendix 2,size,maturation,family,0.120581028,1959,1,0.120581028,male,cross,Actinopteri,between
1928,Oncorhynchus mykiss,60,rayyan-697471502,Untangling the positive genetic correlation between rainbow trout growth and survival,2012,1995-2004,Central Finland,field,male,male,2231,1959,NA,NA,1146,1129,981,889,21992,17938,animal_model,full/half_sib,no,narrow,authors,non_adult,non_adult,male maturity after both 2 and 3 growthing seasons,"male maturity after both 2 and 3 growthing seasons at sea, binary",maturation,maturation,include,cor,0.92,0.02,se,NA,NA,NA,NA,NA,NA,rayyan-697471502,appendix 2,maturation,maturation,family,1.589026915,1959,1,1.589026915,male,non_adult,Actinopteri,within
1929,Oncorhynchus mykiss,47,rayyan-697471388,Quantitative genetics of migration-related traits in rainbow and steelhead trout,2015,1996-2004,southeastern Alaska,field,both,both,NA,NA,NA,NA,NA,NA,NA,NA,15561,15561,animal_model,pedigree,no,narrow,authors,non_adult,both,mature or parr/indeterminate/smolt at month 12,weight at month 15,maturation,size,include,cor,-0.14,"[-0.40, 0.24]",95CI,NA,NA,NA,NA,NA,NA,rayyan-697471388,table s2,maturation,size,pedigree,-0.140925576,15561,1,-0.140925576,both,cross,Actinopteri,between
1930,Oncorhynchus mykiss,47,rayyan-697471388,Quantitative genetics of migration-related traits in rainbow and steelhead trout,2015,1996-2004,southeastern Alaska,field,both,both,NA,NA,NA,NA,NA,NA,NA,NA,15551,15551,animal_model,pedigree,no,narrow,authors,non_adult,both,mature or parr/indeterminate/smolt at month 12,body condition factor (body length to weight) at month 15,maturation,size,include,cor,0.86,"[0.80, 0.96]",95CI,NA,NA,NA,NA,NA,NA,rayyan-697471388,table s2,maturation,size,pedigree,1.293344672,15551,1,1.293344672,both,cross,Actinopteri,between
1931,Oncorhynchus mykiss,47,rayyan-697471388,Quantitative genetics of migration-related traits in rainbow and steelhead trout,2015,1996-2004,southeastern Alaska,field,both,both,NA,NA,NA,NA,NA,NA,NA,NA,15567,15567,animal_model,pedigree,no,narrow,authors,non_adult,both,mature or parr/indeterminate/smolt at month 12,Instantaneous growth rate in length from month 12 to 15,maturation,growth,include,cor,-0.22,"[-0.43, -0.05]",95CI,NA,NA,NA,NA,NA,NA,rayyan-697471388,table s2,maturation,growth,pedigree,-0.223656109,15567,1,-0.223656109,both,cross,Actinopteri,between
1932,Oncorhynchus mykiss,294,rayyan-197247867,Genetic architecture of growth and early life-history transitions in anadromous and derived freshwater populations of steelhead,2004,1996-1998,"Sashin Lake, Alaska, USA",lab,both,both,75,75,NA,NA,41,41,31,31,6570,6565,animal_model,full/half_sib,no,narrow,authors,both,both,daily growth in mass between june and october 1997 (age 1),daily growth in mass between october 1997 and june 1998 (age 1-2),growth,growth,include,cor,-0.083,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-197247867,table 3,growth,growth,family,-0.083191387,75,1,-0.083191387,both,both,Actinopteri,within
1933,Oncorhynchus mykiss,47,rayyan-697471388,Quantitative genetics of migration-related traits in rainbow and steelhead trout,2015,1996-2004,southeastern Alaska,field,both,both,NA,NA,NA,NA,NA,NA,NA,NA,15621,15621,animal_model,pedigree,no,narrow,authors,non_adult,both,mature or parr/indeterminate/smolt at month 12,fork length at month 24,maturation,size,include,cor,-0.559,"[-0.76, -0.22]",95CI,NA,NA,NA,NA,NA,NA,rayyan-697471388,table s2,maturation,size,pedigree,-0.631377497,15621,1,-0.631377497,both,cross,Actinopteri,between
1934,Oncorhynchus mykiss,12,rayyan-178530619,Genetic architecture of rainbow trout survival from egg to adult,2010,1996-2004,Tervo Fisheries Research and Aquaculture station in Central Finland,field,both,both,1618,2231,NA,NA,974,1401,721,981,219951,81499,animal_model,full/half_sib,yes,broad,CC,non_adult,both,survival from 60 post-grading until the start of individual tagging (late),Grow-out survival in freshwater,survival,survival,include,cor,0.27,0.14,se,NA,NA,NA,NA,NA,NA,rayyan-178530619,table 3,survival,survival,family,0.276863823,1618,1,0.276863823,both,cross,Actinopteri,within
1935,Oncorhynchus mykiss,12,rayyan-178530619,Genetic architecture of rainbow trout survival from egg to adult,2010,1996-2004,Tervo Fisheries Research and Aquaculture station in Central Finland,field,both,both,1618,1531,NA,NA,974,772,721,678,219951,40405,animal_model,full/half_sib,yes,broad,CC,non_adult,both,survival from 60 post-grading until the start of individual tagging (late),Grow-out survival in sea water,survival,survival,include,cor,0.33,0.18,se,NA,NA,NA,NA,NA,NA,rayyan-178530619,table 3,survival,survival,family,0.342828254,1531,1,0.342828254,both,cross,Actinopteri,within
1936,Oncorhynchus mykiss,12,rayyan-178530619,Genetic architecture of rainbow trout survival from egg to adult,2010,1996-2004,Tervo Fisheries Research and Aquaculture station in Central Finland,field,both,both,1618,2231,NA,NA,974,1401,721,981,219951,81499,animal_model,full/half_sib,yes,broad,CC,non_adult,both,fingerling survival ,Grow-out survival in freshwater,survival,survival,include,cor,0.09,0.12,se,NA,NA,NA,NA,NA,NA,rayyan-178530619,table 3,survival,survival,family,0.090244188,1618,1,0.090244188,both,cross,Actinopteri,within
1937,Oncorhynchus mykiss,12,rayyan-178530619,Genetic architecture of rainbow trout survival from egg to adult,2010,1996-2004,Tervo Fisheries Research and Aquaculture station in Central Finland,field,both,both,1618,1531,NA,NA,974,772,721,678,219951,40405,animal_model,full/half_sib,yes,broad,CC,non_adult,both,fingerling survival ,Grow-out survival in sea water,survival,survival,include,cor,0.03,0.16,se,NA,NA,NA,NA,NA,NA,rayyan-178530619,table 3,survival,survival,family,0.030009005,1531,1,0.030009005,both,cross,Actinopteri,within
1939,Oncorhynchus mykiss,47,rayyan-697471388,Quantitative genetics of migration-related traits in rainbow and steelhead trout,2015,1996-2004,southeastern Alaska,field,both,both,NA,NA,NA,NA,NA,NA,NA,NA,15639,15639,animal_model,pedigree,no,narrow,authors,both,both,fork length at month 15,Instantaneous growth rate in weight from month 12 to 15,size,growth,include,cor,0.639,0.125,se,NA,NA,NA,NA,NA,NA,rayyan-697471388,table s2,size,growth,pedigree,0.75648181,15639,1,0.75648181,both,both,Actinopteri,between
1940,Oncorhynchus mykiss,47,rayyan-697471388,Quantitative genetics of migration-related traits in rainbow and steelhead trout,2015,1996-2004,southeastern Alaska,field,both,both,NA,NA,NA,NA,NA,NA,NA,NA,15588,15588,animal_model,pedigree,no,narrow,authors,both,both,fork length at month 15,fork length at month 24,size,size,include,cor,0.939,0.022,se,NA,NA,NA,NA,NA,NA,rayyan-697471388,table s2,size,size,pedigree,1.729526896,15588,1,1.729526896,both,both,Actinopteri,within
1941,Oncorhynchus mykiss,47,rayyan-697471388,Quantitative genetics of migration-related traits in rainbow and steelhead trout,2015,1996-2004,southeastern Alaska,field,both,both,NA,NA,NA,NA,NA,NA,NA,NA,15588,15588,animal_model,pedigree,no,narrow,authors,both,both,fork length at month 15,weight at month 24,size,size,include,cor,0.935,0.027,se,NA,NA,NA,NA,NA,NA,rayyan-697471388,table s2,size,size,pedigree,1.696737668,15588,1,1.696737668,both,both,Actinopteri,within
1942,Oncorhynchus mykiss,47,rayyan-697471388,Quantitative genetics of migration-related traits in rainbow and steelhead trout,2015,1996-2004,southeastern Alaska,field,both,both,NA,NA,NA,NA,NA,NA,NA,NA,15581,15581,animal_model,pedigree,no,narrow,authors,both,both,fork length at month 15,body condition factor (body length to weight) at month 24,size,size,include,cor,-0.261,0.131,se,NA,NA,NA,NA,NA,NA,rayyan-697471388,table s2,size,size,pedigree,-0.267181208,15581,1,-0.267181208,both,both,Actinopteri,within
1943,Oncorhynchus mykiss,47,rayyan-697471388,Quantitative genetics of migration-related traits in rainbow and steelhead trout,2015,1996-2004,southeastern Alaska,field,both,both,NA,NA,NA,NA,NA,NA,NA,NA,15588,15588,animal_model,pedigree,no,narrow,authors,both,both,fork length at month 15,Instantaneous growth rate in length from month 15 to 24,size,growth,include,cor,0.261,0.173,se,NA,NA,NA,NA,NA,NA,rayyan-697471388,table s2,size,growth,pedigree,0.267181208,15588,1,0.267181208,both,both,Actinopteri,between
1944,Oncorhynchus mykiss,47,rayyan-697471388,Quantitative genetics of migration-related traits in rainbow and steelhead trout,2015,1996-2004,southeastern Alaska,field,both,both,NA,NA,NA,NA,NA,NA,NA,NA,15562,15562,animal_model,pedigree,no,narrow,authors,both,both,fork length at month 15,Instantaneous growth rate in weightfrom month 15 to 24,size,growth,include,cor,0.072,0.198,se,NA,NA,NA,NA,NA,NA,rayyan-697471388,table s2,size,growth,pedigree,0.072124804,15562,1,0.072124804,both,both,Actinopteri,between
1945,Oncorhynchus mykiss,47,rayyan-697471388,Quantitative genetics of migration-related traits in rainbow and steelhead trout,2015,1996-2004,southeastern Alaska,field,both,both,NA,NA,NA,NA,NA,NA,NA,NA,1976,1976,animal_model,pedigree,no,narrow,authors,both,both,fork length at month 15,measure of overall body at month 24,size,size,include,cor,0.586,0.22,se,NA,NA,NA,NA,NA,NA,rayyan-697471388,table s2,size,size,pedigree,0.671552214,1976,1,0.671552214,both,both,Actinopteri,within
1946,Oncorhynchus mykiss,60,rayyan-697471502,Untangling the positive genetic correlation between rainbow trout growth and survival,2012,1995-2004,Central Finland,field,both,both,1490,2231,NA,NA,772,1401,678,981,40406,189299,animal_model,full/half_sib,no,narrow,authors,both,adult,"their sea grow-out survival between tagging and the end of the grow-out period in sea, binary",weight (fingerlings during tagging),survival,size,include,cor,0.11,0.1,se,NA,NA,NA,NA,NA,NA,rayyan-697471502,table 4,survival,size,family,0.110446916,1490,1,0.110446916,both,cross,Actinopteri,between
1947,Oncorhynchus mykiss,47,rayyan-697471388,Quantitative genetics of migration-related traits in rainbow and steelhead trout,2015,1996-2004,southeastern Alaska,field,both,both,NA,NA,NA,NA,NA,NA,NA,NA,1966,1966,animal_model,pedigree,no,narrow,authors,both,both,Instantaneous growth rate in weightfrom month 15 to 24,measure of overall body at month 24,growth,size,include,cor,0.676,0.102,se,NA,NA,NA,NA,NA,NA,rayyan-697471388,table s2,growth,size,pedigree,0.821710883,1966,1,0.821710883,both,both,Actinopteri,between
1948,Oncorhynchus mykiss,47,rayyan-697471388,Quantitative genetics of migration-related traits in rainbow and steelhead trout,2015,1996-2004,southeastern Alaska,field,both,both,NA,NA,NA,NA,NA,NA,NA,NA,15490,15490,animal_model,pedigree,no,narrow,authors,both,both,fork length at month 12,weight at month 24,size,size,include,cor,0.506,0.15,se,NA,NA,NA,NA,NA,NA,rayyan-697471388,table s2,size,size,pedigree,0.557338446,15490,1,0.557338446,both,both,Actinopteri,within
1949,Oncorhynchus mykiss,47,rayyan-697471388,Quantitative genetics of migration-related traits in rainbow and steelhead trout,2015,1996-2004,southeastern Alaska,field,both,both,NA,NA,NA,NA,NA,NA,NA,NA,15572,15572,animal_model,pedigree,no,narrow,authors,both,both,weight at month 15,fork length at month 24,size,size,include,cor,0.841,0.058,se,NA,NA,NA,NA,NA,NA,rayyan-697471388,table s2,size,size,pedigree,1.22457999,15572,1,1.22457999,both,both,Actinopteri,within
1950,Oncorhynchus mykiss,47,rayyan-697471388,Quantitative genetics of migration-related traits in rainbow and steelhead trout,2015,1996-2004,southeastern Alaska,field,both,both,NA,NA,NA,NA,NA,NA,NA,NA,15572,15572,animal_model,pedigree,no,narrow,authors,both,both,weight at month 15,weight at month 24,size,size,include,cor,0.929,0.03,se,NA,NA,NA,NA,NA,NA,rayyan-697471388,table s2,size,size,pedigree,1.651038568,15572,1,1.651038568,both,both,Actinopteri,within
1951,Oncorhynchus mykiss,60,rayyan-697471502,Untangling the positive genetic correlation between rainbow trout growth and survival,2012,1995-2004,Central Finland,field,both,male,1490,2231,NA,NA,772,1146,678,981,40406,21992,animal_model,full/half_sib,no,narrow,authors,both,non_adult,"their sea grow-out survival between tagging and the end of the grow-out period in sea, binary","male maturity after both 2 and 3 growthing seasons, binary",survival,maturation,include,cor,0.01,0.09,se,NA,NA,NA,NA,NA,NA,rayyan-697471502,table 4,survival,maturation,family,0.010000333,1490,1,0.010000333,male,cross,Actinopteri,between
1952,Oncorhynchus mykiss,47,rayyan-697471388,Quantitative genetics of migration-related traits in rainbow and steelhead trout,2015,1996-2004,southeastern Alaska,field,both,both,NA,NA,NA,NA,NA,NA,NA,NA,15562,15562,animal_model,pedigree,no,narrow,authors,both,both,weight at month 15,Instantaneous growth rate in length from month 15 to 24,size,growth,include,cor,0.0098,0.203,se,NA,NA,NA,NA,NA,NA,rayyan-697471388,table s2,size,growth,pedigree,0.009800314,15562,1,0.009800314,both,both,Actinopteri,between
1953,Oncorhynchus mykiss,47,rayyan-697471388,Quantitative genetics of migration-related traits in rainbow and steelhead trout,2015,1996-2004,southeastern Alaska,field,both,both,NA,NA,NA,NA,NA,NA,NA,NA,15572,15572,animal_model,pedigree,no,narrow,authors,both,both,weight at month 15,Instantaneous growth rate in weightfrom month 15 to 24,size,growth,include,cor,0.021,0.212,se,NA,NA,NA,NA,NA,NA,rayyan-697471388,table s2,size,growth,pedigree,0.021003088,15572,1,0.021003088,both,both,Actinopteri,between
1954,Oncorhynchus mykiss,47,rayyan-697471388,Quantitative genetics of migration-related traits in rainbow and steelhead trout,2015,1996-2004,southeastern Alaska,field,both,both,NA,NA,NA,NA,NA,NA,NA,NA,15996,15996,animal_model,pedigree,no,narrow,authors,both,both,weight at month 12,body condition factor (body length to weight) at month 12,size,size,include,cor,0.142,0.274,se,NA,NA,NA,NA,NA,NA,rayyan-697471388,table s2,size,size,pedigree,0.142966145,15996,1,0.142966145,both,both,Actinopteri,within
1955,Oncorhynchus mykiss,294,rayyan-197247867,Genetic architecture of growth and early life-history transitions in anadromous and derived freshwater populations of steelhead,2004,1996-1998,"Sashin Lake, Alaska, USA",lab,both,both,75,75,NA,NA,41,41,31,31,6593,6586,animal_model,full/half_sib,no,narrow,authors,non_adult,both,proportion smolting at age 2 years,mass in june 1997 (age 1),maturation,size,include,cor,0.012,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-197247867,table 3,maturation,size,family,0.012000576,75,1,0.012000576,both,cross,Actinopteri,between
1956,Oncorhynchus mykiss,47,rayyan-697471388,Quantitative genetics of migration-related traits in rainbow and steelhead trout,2015,1996-2004,southeastern Alaska,field,both,both,NA,NA,NA,NA,NA,NA,NA,NA,15562,15562,animal_model,pedigree,no,narrow,authors,both,both,body condition factor (body length to weight) at month 15,fork length at month 24,size,size,include,cor,-0.069,0.15,se,NA,NA,NA,NA,NA,NA,rayyan-697471388,table s2,size,size,pedigree,-0.069109817,15562,1,-0.069109817,both,both,Actinopteri,within
1957,Oncorhynchus mykiss,294,rayyan-197247867,Genetic architecture of growth and early life-history transitions in anadromous and derived freshwater populations of steelhead,2004,1996-1998,"Sashin Lake, Alaska, USA",lab,both,both,75,75,NA,NA,41,41,31,31,6593,6582,animal_model,full/half_sib,no,narrow,authors,non_adult,both,proportion smolting at age 2 years,mass in june 1998  (age 2),maturation,size,include,cor,-0.482,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-197247867,table 3,maturation,size,family,-0.525586282,75,1,-0.525586282,both,cross,Actinopteri,between
1958,Oncorhynchus mykiss,294,rayyan-197247867,Genetic architecture of growth and early life-history transitions in anadromous and derived freshwater populations of steelhead,2004,1996-1998,"Sashin Lake, Alaska, USA",lab,both,both,75,75,NA,NA,41,41,31,31,6593,6570,animal_model,full/half_sib,no,narrow,authors,non_adult,both,proportion smolting at age 2 years,daily growth in mass between june and october 1997 (age 1),maturation,growth,include,cor,-0.431,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-197247867,table 3,maturation,growth,family,-0.461124173,75,1,-0.461124173,both,cross,Actinopteri,between
1959,Oncorhynchus mykiss,294,rayyan-197247867,Genetic architecture of growth and early life-history transitions in anadromous and derived freshwater populations of steelhead,2004,1996-1998,"Sashin Lake, Alaska, USA",lab,both,both,75,75,NA,NA,41,41,31,31,6593,6565,animal_model,full/half_sib,no,narrow,authors,non_adult,both,proportion smolting at age 2 years,daily growth in mass between october 1997 and june 1998 (age 1-2),maturation,growth,include,cor,-0.086,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-197247867,table 3,maturation,growth,family,-0.086212965,75,1,-0.086212965,both,cross,Actinopteri,between
1960,Oncorhynchus mykiss,294,rayyan-197247867,Genetic architecture of growth and early life-history transitions in anadromous and derived freshwater populations of steelhead,2004,1996-1998,"Sashin Lake, Alaska, USA",lab,both,both,75,75,NA,NA,41,41,31,31,6593,6586,animal_model,full/half_sib,no,narrow,authors,non_adult,both,proportion maturing at age 2 years,mass in june 1997 (age 1),maturation,size,include,cor,-0.184,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-197247867,table 3,maturation,size,family,-0.18611973,75,1,-0.18611973,both,cross,Actinopteri,between
1961,Oncorhynchus mykiss,294,rayyan-197247867,Genetic architecture of growth and early life-history transitions in anadromous and derived freshwater populations of steelhead,2004,1996-1998,"Sashin Lake, Alaska, USA",lab,both,both,75,75,NA,NA,41,41,31,31,6593,6573,animal_model,full/half_sib,no,narrow,authors,non_adult,both,proportion maturing at age 2 years,mass in october 1997  (age 1),maturation,size,include,cor,-0.069,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-197247867,table 3,maturation,size,family,-0.069109817,75,1,-0.069109817,both,cross,Actinopteri,between
1962,Oncorhynchus mykiss,294,rayyan-197247867,Genetic architecture of growth and early life-history transitions in anadromous and derived freshwater populations of steelhead,2004,1996-1998,"Sashin Lake, Alaska, USA",lab,both,both,75,75,NA,NA,41,41,31,31,6593,6582,animal_model,full/half_sib,no,narrow,authors,non_adult,both,proportion maturing at age 2 years,mass in june 1998  (age 2),maturation,size,include,cor,0.2,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-197247867,table 3,maturation,size,family,0.202732554,75,1,0.202732554,both,cross,Actinopteri,between
1963,Oncorhynchus mykiss,294,rayyan-197247867,Genetic architecture of growth and early life-history transitions in anadromous and derived freshwater populations of steelhead,2004,1996-1998,"Sashin Lake, Alaska, USA",lab,both,both,75,75,NA,NA,41,41,31,31,6593,6570,animal_model,full/half_sib,no,narrow,authors,non_adult,both,proportion maturing at age 2 years,daily growth in mass between june and october 1997 (age 1),maturation,growth,include,cor,0.103,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-197247867,table 3,maturation,growth,family,0.103366579,75,1,0.103366579,both,cross,Actinopteri,between
1964,Oncorhynchus mykiss,294,rayyan-197247867,Genetic architecture of growth and early life-history transitions in anadromous and derived freshwater populations of steelhead,2004,1996-1998,"Sashin Lake, Alaska, USA",lab,both,both,75,75,NA,NA,41,41,31,31,6593,6565,animal_model,full/half_sib,no,narrow,authors,non_adult,both,proportion maturing at age 2 years,daily growth in mass between october 1997 and june 1998 (age 1-2),maturation,growth,include,cor,0.511,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-197247867,table 3,maturation,growth,family,0.564082236,75,1,0.564082236,both,cross,Actinopteri,between
1965,Oncorhynchus mykiss,294,rayyan-197247867,Genetic architecture of growth and early life-history transitions in anadromous and derived freshwater populations of steelhead,2004,1996-1998,"Sashin Lake, Alaska, USA",lab,both,both,75,75,NA,NA,41,41,31,31,6586,6573,animal_model,full/half_sib,no,narrow,authors,both,both,mass in june 1997 (age 1),mass in october 1997  (age 1),size,size,include,cor,0.706,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-197247867,table 3,size,size,family,0.87916348,75,1,0.87916348,both,both,Actinopteri,within
1966,Oncorhynchus mykiss,294,rayyan-197247867,Genetic architecture of growth and early life-history transitions in anadromous and derived freshwater populations of steelhead,2004,1996-1998,"Sashin Lake, Alaska, USA",lab,both,both,75,75,NA,NA,41,41,31,31,6586,6582,animal_model,full/half_sib,no,narrow,authors,both,both,mass in june 1997 (age 1),mass in june 1998  (age 2),size,size,include,cor,0.563,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-197247867,table 3,size,size,family,0.637214568,75,1,0.637214568,both,both,Actinopteri,within
1967,Oncorhynchus mykiss,294,rayyan-197247867,Genetic architecture of growth and early life-history transitions in anadromous and derived freshwater populations of steelhead,2004,1996-1998,"Sashin Lake, Alaska, USA",lab,both,both,75,75,NA,NA,41,41,31,31,6586,6570,animal_model,full/half_sib,no,narrow,authors,both,both,mass in june 1997 (age 1),daily growth in mass between june and october 1997 (age 1),size,growth,include,cor,-0.17,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-197247867,table 3,size,growth,family,-0.171666664,75,1,-0.171666664,both,both,Actinopteri,between
1968,Oncorhynchus mykiss,294,rayyan-197247867,Genetic architecture of growth and early life-history transitions in anadromous and derived freshwater populations of steelhead,2004,1996-1998,"Sashin Lake, Alaska, USA",lab,both,both,75,75,NA,NA,41,41,31,31,6586,6565,animal_model,full/half_sib,no,narrow,authors,both,both,mass in june 1997 (age 1),daily growth in mass between october 1997 and june 1998 (age 1-2),size,growth,include,cor,-0.419,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-197247867,table 3,size,growth,family,-0.44647846,75,1,-0.44647846,both,both,Actinopteri,between
1969,Oncorhynchus mykiss,12,rayyan-178530619,Genetic architecture of rainbow trout survival from egg to adult,2010,1996-2004,Tervo Fisheries Research and Aquaculture station in Central Finland,field,both,both,1618,1618,NA,NA,974,974,721,721,249166,219951,animal_model,full/half_sib,yes,broad,CC,non_adult,non_adult,survival until 60 days after grading (early),survival from 60 post-grading until the start of individual tagging (late),survival,survival,include,cor,0.3,0.16,se,NA,NA,NA,NA,NA,NA,rayyan-178530619,table 3,survival,survival,family,0.309519604,1618,1,0.309519604,both,non_adult,Actinopteri,within
1970,Oncorhynchus mykiss,12,rayyan-178530619,Genetic architecture of rainbow trout survival from egg to adult,2010,1996-2004,Tervo Fisheries Research and Aquaculture station in Central Finland,field,both,both,1618,1618,NA,NA,974,974,721,721,249166,219951,animal_model,full/half_sib,yes,broad,CC,non_adult,non_adult,survival until 60 days after grading (early),juvenile fingerling survival,survival,survival,include,cor,0.85,0.05,se,NA,NA,NA,NA,NA,NA,rayyan-178530619,table 3,survival,survival,family,1.256152812,1618,1,1.256152812,both,non_adult,Actinopteri,within
1971,Oncorhynchus mykiss,12,rayyan-178530619,Genetic architecture of rainbow trout survival from egg to adult,2010,1996-2004,Tervo Fisheries Research and Aquaculture station in Central Finland,field,both,both,1618,2231,NA,NA,974,1401,721,981,249166,81499,animal_model,full/half_sib,yes,broad,CC,non_adult,both,survival until 60 days after grading (early),Grow-out survival in freshwater,survival,survival,include,cor,-0.08,0.12,se,NA,NA,NA,NA,NA,NA,rayyan-178530619,table 3,survival,survival,family,-0.080171325,1618,1,-0.080171325,both,cross,Actinopteri,within
1972,Oncorhynchus mykiss,12,rayyan-178530619,Genetic architecture of rainbow trout survival from egg to adult,2010,1996-2004,Tervo Fisheries Research and Aquaculture station in Central Finland,field,both,both,1618,1531,NA,NA,974,772,721,678,249166,40405,animal_model,full/half_sib,yes,broad,CC,non_adult,both,survival until 60 days after grading (early),Grow-out survival in sea water,survival,survival,include,cor,-0.22,0.17,se,NA,NA,NA,NA,NA,NA,rayyan-178530619,table 3,survival,survival,family,-0.223656109,1531,1,-0.223656109,both,cross,Actinopteri,within
1973,Oncorhynchus mykiss,12,rayyan-178530619,Genetic architecture of rainbow trout survival from egg to adult,2010,1996-2004,Tervo Fisheries Research and Aquaculture station in Central Finland,field,both,both,1618,1618,NA,NA,974,974,721,721,219951,219951,animal_model,full/half_sib,yes,broad,CC,non_adult,non_adult,survival from 60 post-grading until the start of individual tagging (late),juvenile fingerling survival,survival,survival,include,cor,0.76,0.08,se,NA,NA,NA,NA,NA,NA,rayyan-178530619,table 3,survival,survival,family,0.996215082,1618,1,0.996215082,both,non_adult,Actinopteri,within
1974,Oncorhynchus mykiss,47,rayyan-697471388,Quantitative genetics of migration-related traits in rainbow and steelhead trout,2015,1996-2004,southeastern Alaska,field,both,both,NA,NA,NA,NA,NA,NA,NA,NA,15502,15502,animal_model,pedigree,no,narrow,authors,non_adult,both,mature or parr/indeterminate/smolt at month 12,Instantaneous growth rate in weight from month 12 to 15,maturation,growth,include,cor,-0.187,"[-0.34, 0.33]",95CI,NA,NA,NA,NA,NA,NA,rayyan-697471388,table s2,maturation,growth,pedigree,-0.189226643,15502,1,-0.189226643,both,cross,Actinopteri,between
1975,Oncorhynchus mykiss,47,rayyan-697471388,Quantitative genetics of migration-related traits in rainbow and steelhead trout,2015,1996-2004,southeastern Alaska,field,both,both,NA,NA,NA,NA,NA,NA,NA,NA,15620,15620,animal_model,pedigree,no,narrow,authors,non_adult,both,mature or parr/indeterminate/smolt at month 12,weight at month 24,maturation,size,include,cor,-0.44,"[-0.67, -0.12]",95CI,NA,NA,NA,NA,NA,NA,rayyan-697471388,table s2,maturation,size,pedigree,-0.472230804,15620,1,-0.472230804,both,cross,Actinopteri,between
1976,Oncorhynchus mykiss,47,rayyan-697471388,Quantitative genetics of migration-related traits in rainbow and steelhead trout,2015,1996-2004,southeastern Alaska,field,both,both,NA,NA,NA,NA,NA,NA,NA,NA,15613,15613,animal_model,pedigree,no,narrow,authors,non_adult,both,mature or parr/indeterminate/smolt at month 12,body condition factor (body length to weight) at month 24,maturation,size,include,cor,0.904,"[0.80, 0.95]",95CI,NA,NA,NA,NA,NA,NA,rayyan-697471388,table s2,maturation,size,pedigree,1.493682012,15613,1,1.493682012,both,cross,Actinopteri,between
1977,Oncorhynchus mykiss,47,rayyan-697471388,Quantitative genetics of migration-related traits in rainbow and steelhead trout,2015,1996-2004,southeastern Alaska,field,both,both,NA,NA,NA,NA,NA,NA,NA,NA,15567,15567,animal_model,pedigree,no,narrow,authors,non_adult,both,mature or parr/indeterminate/smolt at month 12,Instantaneous growth rate in length from month 15 to 24,maturation,growth,include,cor,-0.84,"[-0.91, -0.73]",95CI,NA,NA,NA,NA,NA,NA,rayyan-697471388,table s2,maturation,growth,pedigree,-1.221173518,15567,1,-1.221173518,both,cross,Actinopteri,between
1978,Oncorhynchus mykiss,47,rayyan-697471388,Quantitative genetics of migration-related traits in rainbow and steelhead trout,2015,1996-2004,southeastern Alaska,field,both,both,NA,NA,NA,NA,NA,NA,NA,NA,15550,15550,animal_model,pedigree,no,narrow,authors,non_adult,both,mature or parr/indeterminate/smolt at month 12,Instantaneous growth rate in weightfrom month 15 to 24,maturation,growth,include,cor,-0.784,"[-0.87, -0.61]",95CI,NA,NA,NA,NA,NA,NA,rayyan-697471388,table s2,maturation,growth,pedigree,-1.055667453,15550,1,-1.055667453,both,cross,Actinopteri,between
1979,Oncorhynchus mykiss,47,rayyan-697471388,Quantitative genetics of migration-related traits in rainbow and steelhead trout,2015,1996-2004,southeastern Alaska,field,both,both,NA,NA,NA,NA,NA,NA,NA,NA,1968,1968,animal_model,pedigree,no,narrow,authors,non_adult,both,mature or parr/indeterminate/smolt at month 12,measure of overall body at month 24,maturation,size,include,cor,-0.06,"[-0.59, 0.47]",95CI,NA,NA,NA,NA,NA,NA,rayyan-697471388,table s2,maturation,size,pedigree,-0.060072156,1968,1,-0.060072156,both,cross,Actinopteri,between
1980,Oncorhynchus mykiss,47,rayyan-697471388,Quantitative genetics of migration-related traits in rainbow and steelhead trout,2015,1996-2004,southeastern Alaska,field,both,both,NA,NA,NA,NA,NA,NA,NA,NA,15490,15490,animal_model,pedigree,no,narrow,authors,both,both,fork length at month 12,weight at month 12,size,size,include,cor,0.977,0.02,se,NA,NA,NA,NA,NA,NA,rayyan-697471388,table s2,size,size,pedigree,2.226920804,15490,1,2.226920804,both,both,Actinopteri,within
1981,Oncorhynchus mykiss,47,rayyan-697471388,Quantitative genetics of migration-related traits in rainbow and steelhead trout,2015,1996-2004,southeastern Alaska,field,both,both,NA,NA,NA,NA,NA,NA,NA,NA,15490,15490,animal_model,pedigree,no,narrow,authors,both,both,fork length at month 12,body condition factor (body length to weight) at month 12,size,size,include,cor,-0.138,0.244,se,NA,NA,NA,NA,NA,NA,rayyan-697471388,table s2,size,size,pedigree,-0.138886172,15490,1,-0.138886172,both,both,Actinopteri,within
1982,Oncorhynchus mykiss,47,rayyan-697471388,Quantitative genetics of migration-related traits in rainbow and steelhead trout,2015,1996-2004,southeastern Alaska,field,both,both,NA,NA,NA,NA,NA,NA,NA,NA,15490,15490,animal_model,pedigree,no,narrow,authors,both,both,fork length at month 12,fork length at month 15,size,size,include,cor,0.596,0.139,se,NA,NA,NA,NA,NA,NA,rayyan-697471388,table s2,size,size,pedigree,0.68692045,15490,1,0.68692045,both,both,Actinopteri,within
1983,Oncorhynchus mykiss,47,rayyan-697471388,Quantitative genetics of migration-related traits in rainbow and steelhead trout,2015,1996-2004,southeastern Alaska,field,both,both,NA,NA,NA,NA,NA,NA,NA,NA,15490,15490,animal_model,pedigree,no,narrow,authors,both,both,fork length at month 12,weight at month 15,size,size,include,cor,0.523,0.17,se,NA,NA,NA,NA,NA,NA,rayyan-697471388,table s2,size,size,pedigree,0.580460431,15490,1,0.580460431,both,both,Actinopteri,within
1984,Oncorhynchus mykiss,47,rayyan-697471388,Quantitative genetics of migration-related traits in rainbow and steelhead trout,2015,1996-2004,southeastern Alaska,field,both,both,NA,NA,NA,NA,NA,NA,NA,NA,15490,15490,animal_model,pedigree,no,narrow,authors,both,both,fork length at month 12,body condition factor (body length to weight) at month 15,size,size,include,cor,-0.118,0.19,se,NA,NA,NA,NA,NA,NA,rayyan-697471388,table s2,size,size,pedigree,-0.118552299,15490,1,-0.118552299,both,both,Actinopteri,within
1985,Oncorhynchus mykiss,47,rayyan-697471388,Quantitative genetics of migration-related traits in rainbow and steelhead trout,2015,1996-2004,southeastern Alaska,field,both,both,NA,NA,NA,NA,NA,NA,NA,NA,15490,15490,animal_model,pedigree,no,narrow,authors,both,both,fork length at month 12,Instantaneous growth rate in length from month 12 to 15,size,growth,include,cor,0.429,0.073,se,NA,NA,NA,NA,NA,NA,rayyan-697471388,table s2,size,growth,pedigree,0.458670484,15490,1,0.458670484,both,both,Actinopteri,between
1986,Oncorhynchus mykiss,47,rayyan-697471388,Quantitative genetics of migration-related traits in rainbow and steelhead trout,2015,1996-2004,southeastern Alaska,field,both,both,NA,NA,NA,NA,NA,NA,NA,NA,15490,15490,animal_model,pedigree,no,narrow,authors,both,both,fork length at month 12,Instantaneous growth rate in weight from month 12 to 15,size,growth,include,cor,-0.27,0.184,se,NA,NA,NA,NA,NA,NA,rayyan-697471388,table s2,size,growth,pedigree,-0.276863823,15490,1,-0.276863823,both,both,Actinopteri,between
1987,Oncorhynchus mykiss,60,rayyan-697471502,Untangling the positive genetic correlation between rainbow trout growth and survival,2012,1995-2004,Central Finland,field,both,both,1490,2231,NA,NA,772,1401,678,981,40406,58724,animal_model,full/half_sib,no,narrow,authors,both,adult,"their sea grow-out survival between tagging and the end of the grow-out period in sea, binary",weight during april to june at grow-out period,survival,size,include,cor,-0.05,0.09,se,NA,NA,NA,NA,NA,NA,rayyan-697471502,table 4,survival,size,family,-0.050041729,1490,1,-0.050041729,both,cross,Actinopteri,between
1988,Oncorhynchus mykiss,47,rayyan-697471388,Quantitative genetics of migration-related traits in rainbow and steelhead trout,2015,1996-2004,southeastern Alaska,field,both,both,NA,NA,NA,NA,NA,NA,NA,NA,15685,15685,animal_model,pedigree,no,narrow,authors,both,both,weight at month 15,Instantaneous growth rate in length from month 12 to 15,size,growth,include,cor,0.64,0.14,se,NA,NA,NA,NA,NA,NA,rayyan-697471388,table s2,size,growth,pedigree,0.758173745,15685,1,0.758173745,both,both,Actinopteri,between
1989,Oncorhynchus mykiss,60,rayyan-697471502,Untangling the positive genetic correlation between rainbow trout growth and survival,2012,1995-2004,Central Finland,field,both,both,2231,2231,NA,NA,1401,1401,981,981,189299,58724,animal_model,full/half_sib,no,narrow,authors,non_adult,adult,weight (fingerlings during tagging),weight during april to june at grow-out period,size,size,include,cor,0.37,0.04,se,NA,NA,NA,NA,NA,NA,rayyan-697471502,appendix 2,size,size,family,0.3884231,2231,1,0.3884231,both,cross,Actinopteri,within
1990,Oncorhynchus mykiss,60,rayyan-697471502,Untangling the positive genetic correlation between rainbow trout growth and survival,2012,1995-2004,Central Finland,field,both,both,2231,2231,NA,NA,1401,1401,981,981,189299,45242,animal_model,full/half_sib,no,narrow,authors,non_adult,adult,weight (fingerlings during tagging),weight at 3 year old,size,size,include,cor,0.24,0.05,se,NA,NA,NA,NA,NA,NA,rayyan-697471502,appendix 2,size,size,family,0.244774113,2231,1,0.244774113,both,cross,Actinopteri,within
1991,Oncorhynchus mykiss,60,rayyan-697471502,Untangling the positive genetic correlation between rainbow trout growth and survival,2012,1995-2004,Central Finland,field,both,both,2231,1959,NA,NA,1401,1129,981,889,189299,41678,animal_model,full/half_sib,no,narrow,authors,non_adult,adult,weight (fingerlings during tagging),weight during oct to april at sea grow-out period,size,size,include,cor,0.33,0.05,se,NA,NA,NA,NA,NA,NA,rayyan-697471502,appendix 2,size,size,family,0.342828254,1959,1,0.342828254,both,cross,Actinopteri,within
1992,Oncorhynchus mykiss,60,rayyan-697471502,Untangling the positive genetic correlation between rainbow trout growth and survival,2012,1995-2004,Central Finland,field,both,female,2231,1809,NA,NA,1401,979,981,814,189299,20263,animal_model,full/half_sib,no,narrow,authors,non_adult,non_adult,weight (fingerlings during tagging),"female maturity after both 2 and 3 growthing seasons, binary",size,maturation,include,cor,-0.07,0.06,se,NA,NA,NA,NA,NA,NA,rayyan-697471502,appendix 2,size,maturation,family,-0.070114671,1809,1,-0.070114671,female,non_adult,Actinopteri,between
1993,Oncorhynchus mykiss,47,rayyan-697471388,Quantitative genetics of migration-related traits in rainbow and steelhead trout,2015,1996-2004,southeastern Alaska,field,both,both,NA,NA,NA,NA,NA,NA,NA,NA,1968,1968,animal_model,pedigree,no,narrow,authors,both,both,fork length at month 12,measure of overall body at month 24,size,size,include,cor,-0.533,0.765,se,NA,NA,NA,NA,NA,NA,rayyan-697471388,table s2,size,size,pedigree,-0.594326311,1968,1,-0.594326311,both,both,Actinopteri,within
1994,Oncorhynchus mykiss,47,rayyan-697471388,Quantitative genetics of migration-related traits in rainbow and steelhead trout,2015,1996-2004,southeastern Alaska,field,both,both,NA,NA,NA,NA,NA,NA,NA,NA,15695,15695,animal_model,pedigree,no,narrow,authors,both,both,body condition factor (body length to weight) at month 12,weight at month 15,size,size,include,cor,-0.001,0.093,se,NA,NA,NA,NA,NA,NA,rayyan-697471388,table s2,size,size,pedigree,-0.001,15695,1,-0.001,both,both,Actinopteri,within
1995,Oncorhynchus mykiss,47,rayyan-697471388,Quantitative genetics of migration-related traits in rainbow and steelhead trout,2015,1996-2004,southeastern Alaska,field,both,both,NA,NA,NA,NA,NA,NA,NA,NA,15666,15666,animal_model,pedigree,no,narrow,authors,both,both,weight at month 12,fork length at month 15,size,size,include,cor,0.47,0.19,se,NA,NA,NA,NA,NA,NA,rayyan-697471388,table s2,size,size,pedigree,0.510070337,15666,1,0.510070337,both,both,Actinopteri,within
1996,Oncorhynchus mykiss,47,rayyan-697471388,Quantitative genetics of migration-related traits in rainbow and steelhead trout,2015,1996-2004,southeastern Alaska,field,both,both,NA,NA,NA,NA,NA,NA,NA,NA,15649,15649,animal_model,pedigree,no,narrow,authors,both,both,weight at month 12,weight at month 15,size,size,include,cor,0.37,0.23,se,NA,NA,NA,NA,NA,NA,rayyan-697471388,table s2,size,size,pedigree,0.3884231,15649,1,0.3884231,both,both,Actinopteri,within
1997,Oncorhynchus mykiss,47,rayyan-697471388,Quantitative genetics of migration-related traits in rainbow and steelhead trout,2015,1996-2004,southeastern Alaska,field,both,both,NA,NA,NA,NA,NA,NA,NA,NA,15639,15639,animal_model,pedigree,no,narrow,authors,both,both,weight at month 12,body condition factor (body length to weight) at month 15,size,size,include,cor,-0.023,0.21,se,NA,NA,NA,NA,NA,NA,rayyan-697471388,table s2,size,size,pedigree,-0.023004057,15639,1,-0.023004057,both,both,Actinopteri,within
1998,Oncorhynchus mykiss,60,rayyan-697471502,Untangling the positive genetic correlation between rainbow trout growth and survival,2012,1995-2004,Central Finland,field,both,female,2231,1809,NA,NA,1401,979,981,814,58724,20263,animal_model,full/half_sib,no,narrow,authors,adult,non_adult,weight during april to june at grow-out period,"female maturity after both 2 and 3 growthing seasons, binary",size,maturation,include,cor,0.33,0.05,se,NA,NA,NA,NA,NA,NA,rayyan-697471502,appendix 2,size,maturation,family,0.342828254,1809,1,0.342828254,female,cross,Actinopteri,between
1999,Oncorhynchus mykiss,60,rayyan-697471502,Untangling the positive genetic correlation between rainbow trout growth and survival,2012,1995-2004,Central Finland,field,both,male,2231,2231,NA,NA,1401,1146,981,981,58724,21992,animal_model,full/half_sib,no,narrow,authors,adult,non_adult,weight during april to june at grow-out period,"male maturity after both 2 and 3 growthing seasons, binary",size,maturation,include,cor,0.08,0.05,se,NA,NA,NA,NA,NA,NA,rayyan-697471502,appendix 2,size,maturation,family,0.080171325,2231,1,0.080171325,male,cross,Actinopteri,between
2000,Oncorhynchus mykiss,47,rayyan-697471388,Quantitative genetics of migration-related traits in rainbow and steelhead trout,2015,1996-2004,southeastern Alaska,field,both,both,NA,NA,NA,NA,NA,NA,NA,NA,15584,15584,animal_model,pedigree,no,narrow,authors,both,both,weight at month 12,fork length at month 24,size,size,include,cor,0.248,0.223,se,NA,NA,NA,NA,NA,NA,rayyan-697471388,table s2,size,size,pedigree,0.253280612,15584,1,0.253280612,both,both,Actinopteri,within
2001,Oncorhynchus mykiss,47,rayyan-697471388,Quantitative genetics of migration-related traits in rainbow and steelhead trout,2015,1996-2004,southeastern Alaska,field,both,both,NA,NA,NA,NA,NA,NA,NA,NA,15584,15584,animal_model,pedigree,no,narrow,authors,both,both,weight at month 12,weight at month 24,size,size,include,cor,0.315,0.221,se,NA,NA,NA,NA,NA,NA,rayyan-697471388,table s2,size,size,pedigree,0.326086553,15584,1,0.326086553,both,both,Actinopteri,within
2002,Oncorhynchus mykiss,47,rayyan-697471388,Quantitative genetics of migration-related traits in rainbow and steelhead trout,2015,1996-2004,southeastern Alaska,field,both,both,NA,NA,NA,NA,NA,NA,NA,NA,15577,15577,animal_model,pedigree,no,narrow,authors,both,both,weight at month 12,body condition factor (body length to weight) at month 24,size,size,include,cor,0.226,0.217,se,NA,NA,NA,NA,NA,NA,rayyan-697471388,table s2,size,size,pedigree,0.229970121,15577,1,0.229970121,both,both,Actinopteri,within
2003,Oncorhynchus mykiss,47,rayyan-697471388,Quantitative genetics of migration-related traits in rainbow and steelhead trout,2015,1996-2004,southeastern Alaska,field,both,both,NA,NA,NA,NA,NA,NA,NA,NA,15530,15530,animal_model,pedigree,no,narrow,authors,both,both,weight at month 12,Instantaneous growth rate in length from month 15 to 24,size,growth,include,cor,-0.462,0.24,se,NA,NA,NA,NA,NA,NA,rayyan-697471388,table s2,size,growth,pedigree,-0.49985104,15530,1,-0.49985104,both,both,Actinopteri,between
2004,Oncorhynchus mykiss,47,rayyan-697471388,Quantitative genetics of migration-related traits in rainbow and steelhead trout,2015,1996-2004,southeastern Alaska,field,both,both,NA,NA,NA,NA,NA,NA,NA,NA,15514,15514,animal_model,pedigree,no,narrow,authors,both,both,weight at month 12,Instantaneous growth rate in weightfrom month 15 to 24,size,growth,include,cor,-0.345,0.256,se,NA,NA,NA,NA,NA,NA,rayyan-697471388,table s2,size,growth,pedigree,-0.359757028,15514,1,-0.359757028,both,both,Actinopteri,between
2005,Oncorhynchus mykiss,47,rayyan-697471388,Quantitative genetics of migration-related traits in rainbow and steelhead trout,2015,1996-2004,southeastern Alaska,field,both,both,NA,NA,NA,NA,NA,NA,NA,NA,1974,1974,animal_model,pedigree,no,narrow,authors,both,both,weight at month 12,measure of overall body at month 24,size,size,include,cor,-0.45,0.66,se,NA,NA,NA,NA,NA,NA,rayyan-697471388,table s2,size,size,pedigree,-0.484700279,1974,1,-0.484700279,both,both,Actinopteri,within
2006,Oncorhynchus mykiss,47,rayyan-697471388,Quantitative genetics of migration-related traits in rainbow and steelhead trout,2015,1996-2004,southeastern Alaska,field,both,both,NA,NA,NA,NA,NA,NA,NA,NA,15712,15712,animal_model,pedigree,no,narrow,authors,both,both,body condition factor (body length to weight) at month 12,fork length at month 15,size,size,include,cor,-0.341,0.192,se,NA,NA,NA,NA,NA,NA,rayyan-697471388,table s2,size,size,pedigree,-0.355223674,15712,1,-0.355223674,both,both,Actinopteri,within
2007,Oncorhynchus mykiss,47,rayyan-697471388,Quantitative genetics of migration-related traits in rainbow and steelhead trout,2015,1996-2004,southeastern Alaska,field,both,both,NA,NA,NA,NA,NA,NA,NA,NA,15490,15490,animal_model,pedigree,no,narrow,authors,both,both,fork length at month 12,Instantaneous growth rate in weightfrom month 15 to 24,size,growth,include,cor,-0.221,0.235,se,NA,NA,NA,NA,NA,NA,rayyan-697471388,table s2,size,growth,pedigree,-0.224707214,15490,1,-0.224707214,both,both,Actinopteri,between
2008,Oncorhynchus mykiss,47,rayyan-697471388,Quantitative genetics of migration-related traits in rainbow and steelhead trout,2015,1996-2004,southeastern Alaska,field,both,both,NA,NA,NA,NA,NA,NA,NA,NA,15685,15685,animal_model,pedigree,no,narrow,authors,both,both,body condition factor (body length to weight) at month 12,body condition factor (body length to weight) at month 15,size,size,include,cor,0.797,0.12,se,NA,NA,NA,NA,NA,NA,rayyan-697471388,table s2,size,size,pedigree,1.090333954,15685,1,1.090333954,both,both,Actinopteri,within
2009,Oncorhynchus mykiss,294,rayyan-197247867,Genetic architecture of growth and early life-history transitions in anadromous and derived freshwater populations of steelhead,2004,1996-1998,"Sashin Lake, Alaska, USA",lab,both,both,75,75,NA,NA,41,41,31,31,6573,6582,animal_model,full/half_sib,no,narrow,authors,both,both,mass in october 1997  (age 1),mass in june 1998  (age 2),size,size,include,cor,0.934,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-197247867,table 3,size,size,family,1.688845467,75,1,1.688845467,both,both,Actinopteri,within
2010,Oncorhynchus mykiss,47,rayyan-697471388,Quantitative genetics of migration-related traits in rainbow and steelhead trout,2015,1996-2004,southeastern Alaska,field,both,both,NA,NA,NA,NA,NA,NA,NA,NA,15642,15642,animal_model,pedigree,no,narrow,authors,both,both,body condition factor (body length to weight) at month 12,Instantaneous growth rate in weight from month 12 to 15,size,growth,include,cor,-0.273,0.18,se,NA,NA,NA,NA,NA,NA,rayyan-697471388,table s2,size,growth,pedigree,-0.280102561,15642,1,-0.280102561,both,both,Actinopteri,between
2011,Oncorhynchus mykiss,47,rayyan-697471388,Quantitative genetics of migration-related traits in rainbow and steelhead trout,2015,1996-2004,southeastern Alaska,field,both,both,NA,NA,NA,NA,NA,NA,NA,NA,15630,15630,animal_model,pedigree,no,narrow,authors,both,both,body condition factor (body length to weight) at month 12,fork length at month 24,size,size,include,cor,-0.311,0.182,se,NA,NA,NA,NA,NA,NA,rayyan-697471388,table s2,size,size,pedigree,-0.321652106,15630,1,-0.321652106,both,both,Actinopteri,within
2012,Oncorhynchus mykiss,47,rayyan-697471388,Quantitative genetics of migration-related traits in rainbow and steelhead trout,2015,1996-2004,southeastern Alaska,field,both,both,NA,NA,NA,NA,NA,NA,NA,NA,15630,15630,animal_model,pedigree,no,narrow,authors,both,both,body condition factor (body length to weight) at month 12,weight at month 24,size,size,include,cor,-0.115,0.203,se,NA,NA,NA,NA,NA,NA,rayyan-697471388,table s2,size,size,pedigree,-0.115511019,15630,1,-0.115511019,both,both,Actinopteri,within
2013,Oncorhynchus mykiss,47,rayyan-697471388,Quantitative genetics of migration-related traits in rainbow and steelhead trout,2015,1996-2004,southeastern Alaska,field,both,both,NA,NA,NA,NA,NA,NA,NA,NA,15623,15623,animal_model,pedigree,no,narrow,authors,both,both,body condition factor (body length to weight) at month 12,body condition factor (body length to weight) at month 24,size,size,include,cor,0.781,0.11,se,NA,NA,NA,NA,NA,NA,rayyan-697471388,table s2,size,size,pedigree,1.047929277,15623,1,1.047929277,both,both,Actinopteri,within
2014,Oncorhynchus mykiss,47,rayyan-697471388,Quantitative genetics of migration-related traits in rainbow and steelhead trout,2015,1996-2004,southeastern Alaska,field,both,both,NA,NA,NA,NA,NA,NA,NA,NA,15576,15576,animal_model,pedigree,no,narrow,authors,both,both,body condition factor (body length to weight) at month 12,Instantaneous growth rate in length from month 15 to 24,size,growth,include,cor,-0.091,0.21,se,NA,NA,NA,NA,NA,NA,rayyan-697471388,table s2,size,growth,pedigree,-0.091252446,15576,1,-0.091252446,both,both,Actinopteri,between
2015,Oncorhynchus mykiss,47,rayyan-697471388,Quantitative genetics of migration-related traits in rainbow and steelhead trout,2015,1996-2004,southeastern Alaska,field,both,both,NA,NA,NA,NA,NA,NA,NA,NA,15560,15560,animal_model,pedigree,no,narrow,authors,both,both,body condition factor (body length to weight) at month 12,Instantaneous growth rate in weightfrom month 15 to 24,size,growth,include,cor,0.064,0.22,se,NA,NA,NA,NA,NA,NA,rayyan-697471388,table s2,size,growth,pedigree,0.064087597,15560,1,0.064087597,both,both,Actinopteri,between
2016,Oncorhynchus mykiss,47,rayyan-697471388,Quantitative genetics of migration-related traits in rainbow and steelhead trout,2015,1996-2004,southeastern Alaska,field,both,both,NA,NA,NA,NA,NA,NA,NA,NA,1980,1980,animal_model,pedigree,no,narrow,authors,both,both,body condition factor (body length to weight) at month 12,measure of overall body at month 24,size,size,include,cor,-0.008,0.18,se,NA,NA,NA,NA,NA,NA,rayyan-697471388,table s2,size,size,pedigree,-0.008000171,1980,1,-0.008000171,both,both,Actinopteri,within
2017,Oncorhynchus mykiss,47,rayyan-697471388,Quantitative genetics of migration-related traits in rainbow and steelhead trout,2015,1996-2004,southeastern Alaska,field,both,both,NA,NA,NA,NA,NA,NA,NA,NA,15697,15697,animal_model,pedigree,no,narrow,authors,both,both,fork length at month 15,weight at month 15,size,size,include,cor,0.976,0.015,se,NA,NA,NA,NA,NA,NA,rayyan-697471388,table s2,size,size,pedigree,2.205388024,15697,1,2.205388024,both,both,Actinopteri,within
2018,Oncorhynchus mykiss,47,rayyan-697471388,Quantitative genetics of migration-related traits in rainbow and steelhead trout,2015,1996-2004,southeastern Alaska,field,both,both,NA,NA,NA,NA,NA,NA,NA,NA,15697,15697,animal_model,pedigree,no,narrow,authors,both,both,fork length at month 15,body condition factor (body length to weight) at month 15,size,size,include,cor,-0.115,0.163,se,NA,NA,NA,NA,NA,NA,rayyan-697471388,table s2,size,size,pedigree,-0.115511019,15697,1,-0.115511019,both,both,Actinopteri,within
2019,Oncorhynchus mykiss,47,rayyan-697471388,Quantitative genetics of migration-related traits in rainbow and steelhead trout,2015,1996-2004,southeastern Alaska,field,both,both,NA,NA,NA,NA,NA,NA,NA,NA,15712,15712,animal_model,pedigree,no,narrow,authors,both,both,fork length at month 15,Instantaneous growth rate in length from month 12 to 15,size,growth,include,cor,0.607,0.134,se,NA,NA,NA,NA,NA,NA,rayyan-697471388,table s2,size,growth,pedigree,0.704157377,15712,1,0.704157377,both,both,Actinopteri,between
2020,Oncorhynchus mykiss,47,rayyan-697471388,Quantitative genetics of migration-related traits in rainbow and steelhead trout,2015,1996-2004,southeastern Alaska,field,both,both,NA,NA,NA,NA,NA,NA,NA,NA,15490,15490,animal_model,pedigree,no,narrow,authors,both,both,fork length at month 12,Instantaneous growth rate in length from month 15 to 24,size,growth,include,cor,-0.222,0.22,se,NA,NA,NA,NA,NA,NA,rayyan-697471388,table s2,size,growth,pedigree,-0.225758808,15490,1,-0.225758808,both,both,Actinopteri,between
2021,Oncorhynchus mykiss,105,rayyan-697471793,The genetic architecture of correlations among growth-related traits and male age at maturation in rainbow trout,2003,1993-1999,"Ontario, Canada",lab,both,both,188,188,2,2,NA,NA,NA,NA,1382,1381,animal_model,half_sib,no,narrow,authors,non_adult,non_adult,210 dpf body mass,Fulton’s condition factor,size,size,include,cor,0.035,0.028,se,NA,NA,NA,NA,NA,NA,rayyan-697471793,table 4,size,size,family,0.035014302,188,1,0.035014302,both,non_adult,Actinopteri,within
2022,Oncorhynchus mykiss,105,rayyan-697471793,The genetic architecture of correlations among growth-related traits and male age at maturation in rainbow trout,2003,1993-1999,"Ontario, Canada",lab,both,both,188,188,2,2,NA,NA,NA,NA,1382,1381,animal_model,half_sib,no,narrow,authors,non_adult,non_adult,210 dpf body mass,Fulton’s condition factor,size,size,include,cor,0.261,0.03,se,NA,NA,NA,NA,NA,NA,rayyan-697471793,table 4,size,size,family,0.267181208,188,1,0.267181208,both,non_adult,Actinopteri,within
2023,Oncorhynchus mykiss,47,rayyan-697471388,Quantitative genetics of migration-related traits in rainbow and steelhead trout,2015,1996-2004,southeastern Alaska,field,both,both,NA,NA,NA,NA,NA,NA,NA,NA,15712,15712,animal_model,pedigree,no,narrow,authors,both,both,body condition factor (body length to weight) at month 12,Instantaneous growth rate in length from month 12 to 15,size,growth,include,cor,-0.225,0.194,se,NA,NA,NA,NA,NA,NA,rayyan-697471388,table s2,size,growth,pedigree,-0.228916547,15712,1,-0.228916547,both,both,Actinopteri,between
2024,Oncorhynchus mykiss,294,rayyan-197247867,Genetic architecture of growth and early life-history transitions in anadromous and derived freshwater populations of steelhead,2004,1996-1998,"Sashin Lake, Alaska, USA",lab,both,both,75,75,NA,NA,41,41,31,31,6593,6573,animal_model,full/half_sib,no,narrow,authors,non_adult,both,proportion smolting at age 2 years,mass in october 1997  (age 1),maturation,size,include,cor,-0.312,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-197247867,table 3,maturation,size,family,-0.322759566,75,1,-0.322759566,both,cross,Actinopteri,between
2025,Oncorhynchus mykiss,47,rayyan-697471388,Quantitative genetics of migration-related traits in rainbow and steelhead trout,2015,1996-2004,southeastern Alaska,field,both,both,NA,NA,NA,NA,NA,NA,NA,NA,15649,15649,animal_model,pedigree,no,narrow,authors,both,both,weight at month 15,Instantaneous growth rate in weight from month 12 to 15,size,growth,include,cor,0.681,0.13,se,NA,NA,NA,NA,NA,NA,rayyan-697471388,table s2,size,growth,pedigree,0.830976515,15649,1,0.830976515,both,both,Actinopteri,between
2026,Oncorhynchus mykiss,105,rayyan-697471793,The genetic architecture of correlations among growth-related traits and male age at maturation in rainbow trout,2003,1993-1999,"Ontario, Canada",lab,both,both,188,188,2,2,NA,NA,NA,NA,1381,1404,animal_model,half_sib,no,narrow,authors,non_adult,non_adult,Fulton’s condition factor,precocious maturation,size,maturation,include,cor,0.07,0.034,se,NA,NA,NA,NA,NA,NA,rayyan-697471793,table 4,size,maturation,family,0.070114671,188,1,0.070114671,both,non_adult,Actinopteri,between
2027,Oncorhynchus mykiss,47,rayyan-697471388,Quantitative genetics of migration-related traits in rainbow and steelhead trout,2015,1996-2004,southeastern Alaska,field,both,both,NA,NA,NA,NA,NA,NA,NA,NA,15697,15697,animal_model,pedigree,no,narrow,authors,both,both,weight at month 15,body condition factor (body length to weight) at month 15,size,size,include,cor,0.094,0.182,se,NA,NA,NA,NA,NA,NA,rayyan-697471388,table s2,size,size,pedigree,0.094278338,15697,1,0.094278338,both,both,Actinopteri,within
2028,Oncorhynchus mykiss,47,rayyan-697471388,Quantitative genetics of migration-related traits in rainbow and steelhead trout,2015,1996-2004,southeastern Alaska,field,both,both,NA,NA,NA,NA,NA,NA,NA,NA,15490,15490,animal_model,pedigree,no,narrow,authors,both,both,fork length at month 12,fork length at month 24,size,size,include,cor,0.478,0.153,se,NA,NA,NA,NA,NA,NA,rayyan-697471388,table s2,size,size,pedigree,0.520388757,15490,1,0.520388757,both,both,Actinopteri,within
2029,Oncorhynchus mykiss,47,rayyan-697471388,Quantitative genetics of migration-related traits in rainbow and steelhead trout,2015,1996-2004,southeastern Alaska,field,both,both,NA,NA,NA,NA,NA,NA,NA,NA,15649,15649,animal_model,pedigree,no,narrow,authors,both,both,weight at month 12,Instantaneous growth rate in weight from month 12 to 15,size,growth,include,cor,-0.404,0.19,se,NA,NA,NA,NA,NA,NA,rayyan-697471388,table s2,size,growth,pedigree,-0.428419959,15649,1,-0.428419959,both,both,Actinopteri,between
2030,Oncorhynchus mykiss,47,rayyan-697471388,Quantitative genetics of migration-related traits in rainbow and steelhead trout,2015,1996-2004,southeastern Alaska,field,both,both,NA,NA,NA,NA,NA,NA,NA,NA,15490,15490,animal_model,pedigree,no,narrow,authors,both,both,fork length at month 12,body condition factor (body length to weight) at month 24,size,size,include,cor,-0.0972,0.179,se,NA,NA,NA,NA,NA,NA,rayyan-697471388,table s2,size,size,pedigree,-0.097507857,15490,1,-0.097507857,both,both,Actinopteri,within
2031,Oncorhynchus mykiss,47,rayyan-697471388,Quantitative genetics of migration-related traits in rainbow and steelhead trout,2015,1996-2004,southeastern Alaska,field,both,both,NA,NA,NA,NA,NA,NA,NA,NA,15565,15565,animal_model,pedigree,no,narrow,authors,both,both,weight at month 15,body condition factor (body length to weight) at month 24,size,size,include,cor,0.007,0.174,se,NA,NA,NA,NA,NA,NA,rayyan-697471388,table s2,size,size,pedigree,0.007000114,15565,1,0.007000114,both,both,Actinopteri,within
2032,Oncorhynchus mykiss,47,rayyan-697471388,Quantitative genetics of migration-related traits in rainbow and steelhead trout,2015,1996-2004,southeastern Alaska,field,both,both,NA,NA,NA,NA,NA,NA,NA,NA,15659,15659,animal_model,pedigree,no,narrow,authors,both,both,weight at month 12,Instantaneous growth rate in length from month 12 to 15,size,growth,include,cor,-0.396,0.195,se,NA,NA,NA,NA,NA,NA,rayyan-697471388,table s2,size,growth,pedigree,-0.418896043,15659,1,-0.418896043,both,both,Actinopteri,between
2037,Oncorhynchus nerka,132,rayyan-697471998,It's a bear market: evolutionary and ecological effects of predation on two wild sockeye salmon populations,2016,"2004-2005, 2008-2010",Wood River Lakes system in southwestern Alaska,field,both,both,NA,NA,NA,NA,NA,NA,NA,NA,2323,2323,animal_model,pedigree,no,narrow,authors,both,adult,lifespan,body length,survival,size,include,cor,0.51,"[-0.176, 0.895]",95CI,NA,NA,NA,NA,NA,NA,Creek_A,supplementary table 4,survival,size,pedigree,0.562729769,2323,1,0.562729769,both,cross,Actinopteri,between
2038,Oncorhynchus nerka,132,rayyan-697471998,It's a bear market: evolutionary and ecological effects of predation on two wild sockeye salmon populations,2016,"2004-2005, 2008-2010",Wood River Lakes system in southwestern Alaska,field,both,both,NA,NA,NA,NA,NA,NA,NA,NA,2023,2023,animal_model,pedigree,no,narrow,authors,both,adult,lifespan,standardized body depth,survival,size,include,cor,0.389,"[0.036, 0.734]",95CI,NA,NA,NA,NA,NA,NA,Creek_C,supplementary table 4,survival,size,pedigree,0.410621192,2023,1,0.410621192,both,cross,Actinopteri,between
2041,Oncorhynchus nerka,132,rayyan-697471998,It's a bear market: evolutionary and ecological effects of predation on two wild sockeye salmon populations,2016,"2004-2005, 2008-2010",Wood River Lakes system in southwestern Alaska,field,both,both,NA,NA,NA,NA,NA,NA,NA,NA,2023,2023,animal_model,pedigree,no,narrow,authors,both,adult,lifespan,body depth ,survival,size,include,cor,-0.237,"[-0.547, 0.055]",95CI,NA,NA,NA,NA,NA,NA,Creek_C,supplementary table 4,survival,size,pedigree,-0.241593171,2023,1,-0.241593171,both,cross,Actinopteri,between
2043,Oncorhynchus nerka,132,rayyan-697471998,It's a bear market: evolutionary and ecological effects of predation on two wild sockeye salmon populations,2016,"2004-2005, 2008-2010",Wood River Lakes system in southwestern Alaska,field,both,both,NA,NA,NA,NA,NA,NA,NA,NA,2323,2323,animal_model,pedigree,no,narrow,authors,both,adult,lifespan,standardized body depth,survival,size,include,cor,0.405,"[-0.510, 0.986]",95CI,NA,NA,NA,NA,NA,NA,Creek_A,supplementary table 4,survival,size,pedigree,0.429615588,2323,1,0.429615588,both,cross,Actinopteri,between
2045,Oncorhynchus nerka,132,rayyan-697471998,It's a bear market: evolutionary and ecological effects of predation on two wild sockeye salmon populations,2016,"2004-2005, 2008-2010",Wood River Lakes system in southwestern Alaska,field,both,both,NA,NA,NA,NA,NA,NA,NA,NA,2323,2323,animal_model,pedigree,no,narrow,authors,both,adult,lifespan,body depth ,survival,size,include,cor,0.622,"[-0.209, 0.99]",95CI,NA,NA,NA,NA,NA,NA,Creek_A,supplementary table 4,survival,size,pedigree,0.72826052,2323,1,0.72826052,both,cross,Actinopteri,between
2046,Oncorhynchus nerka,132,rayyan-697471998,It's a bear market: evolutionary and ecological effects of predation on two wild sockeye salmon populations,2016,"2004-2005, 2008-2010",Wood River Lakes system in southwestern Alaska,field,both,both,NA,NA,NA,NA,NA,NA,NA,NA,2023,2023,animal_model,pedigree,no,narrow,authors,both,adult,lifespan,body length,survival,size,include,cor,-0.623,"[-0.842, -0.342]",95CI,NA,NA,NA,NA,NA,NA,Creek_C,supplementary table 4,survival,size,pedigree,-0.72989319,2023,1,-0.72989319,both,cross,Actinopteri,between
2047,Orchesella cincta,67,rayyan-697471600,Genetic correlation between temperature-induced plasticity of life-history traits in a soil arthropod,2011,NA,NA,lab,both,both,97,92,19,19,97,92,97,92,516,416,line_mean_correlation,genetic_line,no,broad,CC,non_adult,non_adult,egg development rate (the inverse of the time between laying and hatching),juvenile growth rate (the natural logarithm of the wet weight divided by the time between hatching and weighing),maturation,growth,include,cor,0.122,NA,NA,NA,NA,NA,NA,NA,NA,low,table 2,maturation,growth,genotype,0.122610746,19,1,0.122610746,both,non_adult,Collembola,between
2048,Orchesella cincta,67,rayyan-697471600,Genetic correlation between temperature-induced plasticity of life-history traits in a soil arthropod,2011,NA,NA,lab,both,both,97,69,18,18,97,69,97,69,516,1329,line_mean_correlation,genetic_line,no,broad,CC,non_adult,non_adult,egg development rate (the inverse of the time between laying and hatching),egg size,maturation,size,include,cor,-0.24,NA,NA,NA,NA,NA,NA,NA,NA,low,table 2,maturation,size,genotype,-0.244774113,18,1,-0.244774113,both,non_adult,Collembola,between
2049,Orchesella cincta,67,rayyan-697471600,Genetic correlation between temperature-induced plasticity of life-history traits in a soil arthropod,2011,NA,NA,lab,both,both,92,69,18,18,92,69,92,69,416,1329,line_mean_correlation,genetic_line,no,broad,CC,non_adult,non_adult,juvenile growth rate (the natural logarithm of the wet weight divided by the time between hatching and weighing),egg size,growth,size,include,cor,0.034,NA,NA,NA,NA,NA,NA,NA,NA,low,table 2,growth,size,genotype,0.03401311,18,1,0.03401311,both,non_adult,Collembola,between
2050,Orchesella cincta,67,rayyan-697471600,Genetic correlation between temperature-induced plasticity of life-history traits in a soil arthropod,2011,NA,NA,lab,both,both,92,69,18,18,92,69,92,69,416,1329,line_mean_correlation,genetic_line,no,broad,CC,non_adult,non_adult,juvenile growth rate (the natural logarithm of the wet weight divided by the time between hatching and weighing),egg size,growth,size,include,cor,-0.024,NA,NA,NA,NA,NA,NA,NA,NA,high,table 2,growth,size,genotype,-0.02400461,18,1,-0.02400461,both,non_adult,Collembola,between
2051,Orchesella cincta,67,rayyan-697471600,Genetic correlation between temperature-induced plasticity of life-history traits in a soil arthropod,2011,NA,NA,lab,both,both,97,92,19,19,97,92,97,92,516,416,line_mean_correlation,genetic_line,no,broad,CC,non_adult,non_adult,egg development rate (the inverse of the time between laying and hatching),juvenile growth rate (the natural logarithm of the wet weight divided by the time between hatching and weighing),maturation,growth,include,cor,0.282,NA,NA,NA,NA,NA,NA,NA,NA,high,table 2,maturation,growth,genotype,0.289853534,19,1,0.289853534,both,non_adult,Collembola,between
2052,Orchesella cincta,67,rayyan-697471600,Genetic correlation between temperature-induced plasticity of life-history traits in a soil arthropod,2011,NA,NA,lab,both,both,97,69,18,18,97,69,97,69,516,1329,line_mean_correlation,genetic_line,no,broad,CC,non_adult,non_adult,egg development rate (the inverse of the time between laying and hatching),egg size,maturation,size,include,cor,0.204,NA,NA,NA,NA,NA,NA,NA,NA,high,table 2,maturation,size,genotype,0.20690272,18,1,0.20690272,both,non_adult,Collembola,between
2053,Oreochromis niloticus,174,rayyan-197247104,Genetic parameters for reproductive traits in female Nile tilapia (Oreochromis niloticus): I. Spawning success and time to spawn,2013,2008-2011,NA,lab,female,female,NA,NA,NA,NA,NA,NA,NA,NA,914,914,animal_model,pedigree,no,narrow,authors,adult,adult,spawn or not ,harvest weight,fertility,size,include_2,cor,0.51,0.17,se,NA,NA,NA,NA,NA,NA,logit_model_day_20,table 6,fertility,size,pedigree,0.562729769,914,1,0.562729769,female,adult,Actinopteri,between
2054,Oreochromis niloticus,174,rayyan-197247104,Genetic parameters for reproductive traits in female Nile tilapia (Oreochromis niloticus): I. Spawning success and time to spawn,2013,2008-2011,NA,lab,female,female,NA,NA,NA,NA,NA,NA,NA,NA,914,914,animal_model,pedigree,no,narrow,authors,adult,adult,spawn or not ,harvest weight,fertility,size,include_2,cor,0.45,0.17,se,NA,NA,NA,NA,NA,NA,logit_model_day_24,table 6,fertility,size,pedigree,0.484700279,914,1,0.484700279,female,adult,Actinopteri,between
2059,Oreochromis niloticus,174,rayyan-197247104,Genetic parameters for reproductive traits in female Nile tilapia (Oreochromis niloticus): I. Spawning success and time to spawn,2013,2008-2011,NA,lab,female,female,NA,NA,NA,NA,NA,NA,NA,NA,914,914,animal_model,pedigree,no,narrow,authors,adult,adult,spawn or not ,harvest weight,fertility,size,include_2,cor,0.63,0.22,se,NA,NA,NA,NA,NA,NA,logit_model_day_16,table 6,fertility,size,pedigree,0.741416144,914,1,0.741416144,female,adult,Actinopteri,between
2062,Oreochromis niloticus,174,rayyan-197247104,Genetic parameters for reproductive traits in female Nile tilapia (Oreochromis niloticus): I. Spawning success and time to spawn,2013,2008-2011,NA,lab,female,female,NA,NA,NA,NA,NA,NA,NA,NA,914,914,animal_model,pedigree,no,narrow,authors,adult,adult,spawn or not ,harvest weight,fertility,size,include_2,cor,0.83,0.48,se,NA,NA,NA,NA,NA,NA,logit_model_day_12,table 6,fertility,size,pedigree,1.188136404,914,1,1.188136404,female,adult,Actinopteri,between
2063,Oreochromis niloticus,174,rayyan-197247104,Genetic parameters for reproductive traits in female Nile tilapia (Oreochromis niloticus): I. Spawning success and time to spawn,2013,2008-2011,NA,lab,female,female,NA,NA,NA,NA,NA,NA,NA,NA,914,914,animal_model,pedigree,no,narrow,authors,adult,adult,spawn or not ,harvest weight,fertility,size,include_2,cor,0.47,0.18,se,NA,NA,NA,NA,NA,NA,logit_model_day_32,table 6,fertility,size,pedigree,0.510070337,914,1,0.510070337,female,adult,Actinopteri,between
2064,Oreochromis niloticus,174,rayyan-197247104,Genetic parameters for reproductive traits in female Nile tilapia (Oreochromis niloticus): I. Spawning success and time to spawn,2013,2008-2011,NA,lab,female,female,NA,NA,NA,NA,NA,NA,NA,NA,914,914,animal_model,pedigree,no,narrow,authors,adult,adult,spawn or not ,harvest weight,fertility,size,include_2,cor,0.41,0.19,se,NA,NA,NA,NA,NA,NA,logit_model_day_28,table 6,fertility,size,pedigree,0.435611223,914,1,0.435611223,female,adult,Actinopteri,between
2065,Oryzias latipes,311,rayyan-697472406,Unidirectional response to bidirectional selection on body size II. Quantitative genetics,2020,2011,"Kiyosu, Japan",lab,both,both,45,45,3,3,45,45,45,45,5285,5285,animal_model,full_sib,yes,narrow,authors,both,non_adult,body length at day 75,maturity status,size,maturation,include,cor,0.65,"[0.31, 0.81]",95CI,NA,NA,NA,NA,NA,NA,rayyan-697472406,table 1,size,maturation,family,0.775298706,45,1,0.775298706,both,cross,Actinopteri,between
2068,Ovis canadensis,112,rayyan-697471828,Quantitative genetics of life-history traits in a long-lived wild mammal,2000,1973-1998,"Ram Mountain, Alberta",field,female,female,66,34,NA,NA,66,34,NA,NA,175,103,parent_offspring_regression,parent_offspring_pair,no,narrow,authors,non_adult,adult,1/age at primiparity,weaning success after 7 years of age,maturation,fertility,include,cor,0.52,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-697471828,table 4,maturation,fertility,family,0.576339755,34,1,0.576339755,female,cross,Mammalia,between
2069,Ovis canadensis,112,rayyan-697471828,Quantitative genetics of life-history traits in a long-lived wild mammal,2000,1973-1998,"Ram Mountain, Alberta",field,female,female,66,85,NA,NA,66,85,NA,NA,175,200,parent_offspring_regression,parent_offspring_pair,no,narrow,authors,non_adult,adult,1/age at primiparity,adult body mass,maturation,size,include,cor,-0.22,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-697471828,table 4,maturation,size,family,-0.223656109,66,1,-0.223656109,female,cross,Mammalia,between
2070,Ovis canadensis,112,rayyan-697471828,Quantitative genetics of life-history traits in a long-lived wild mammal,2000,1973-1998,"Ram Mountain, Alberta",field,female,female,66,72,NA,NA,66,72,NA,NA,175,174,parent_offspring_regression,parent_offspring_pair,no,narrow,authors,non_adult,adult,1/age at primiparity,weaning success between 2 and 7 years of age,maturation,fertility,include,cor,0.96,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-697471828,table 4,maturation,fertility,family,1.945910149,66,1,1.945910149,female,cross,Mammalia,between
2071,Ovis canadensis,112,rayyan-697471828,Quantitative genetics of life-history traits in a long-lived wild mammal,2000,1973-1998,"Ram Mountain, Alberta",field,female,female,66,72,NA,NA,66,72,NA,NA,175,174,parent_offspring_regression,parent_offspring_pair,no,narrow,authors,non_adult,adult,1/age at primiparity,reproductive success between 2 and 7 years of age,maturation,fertility,include,cor,NA,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-697471828,table 4,maturation,fertility,family,NA,66,1,NA,female,cross,Mammalia,between
2072,Ovis canadensis,112,rayyan-697471828,Quantitative genetics of life-history traits in a long-lived wild mammal,2000,1973-1998,"Ram Mountain, Alberta",field,female,female,85,72,NA,NA,85,72,NA,NA,218,174,parent_offspring_regression,parent_offspring_pair,no,narrow,authors,both,adult,longevity,reproductive success between 2 and 7 years of age,survival,fertility,include,cor,0.83,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-697471828,table 4,survival,fertility,family,1.188136404,72,1,1.188136404,female,cross,Mammalia,between
2073,Ovis canadensis,112,rayyan-697471828,Quantitative genetics of life-history traits in a long-lived wild mammal,2000,1973-1998,"Ram Mountain, Alberta",field,female,female,66,66,NA,NA,66,66,NA,NA,163,163,parent_offspring_regression,parent_offspring_pair,no,narrow,authors,adult,adult,lifetime fecundity,lifetime weaning success,fertility,fertility,include,cor,0.99,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-697471828,table 4,fertility,fertility,family,2.646652412,66,1,2.646652412,female,adult,Mammalia,within
2074,Ovis canadensis,112,rayyan-697471828,Quantitative genetics of life-history traits in a long-lived wild mammal,2000,1973-1998,"Ram Mountain, Alberta",field,female,female,66,72,NA,NA,66,72,NA,NA,175,174,parent_offspring_regression,parent_offspring_pair,no,narrow,authors,non_adult,adult,1/age at primiparity,fecundity between 2 and 7 years of age,maturation,fertility,include,cor,NA,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-697471828,table 4,maturation,fertility,family,NA,66,1,NA,female,cross,Mammalia,between
2075,Ovis canadensis,112,rayyan-697471828,Quantitative genetics of life-history traits in a long-lived wild mammal,2000,1973-1998,"Ram Mountain, Alberta",field,female,female,66,34,NA,NA,66,34,NA,NA,163,103,parent_offspring_regression,parent_offspring_pair,no,narrow,authors,adult,adult,lifetime weaning success,weaning success after 7 years of age,fertility,fertility,include,cor,NA,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-697471828,table 4,fertility,fertility,family,NA,34,1,NA,female,adult,Mammalia,within
2076,Ovis canadensis,112,rayyan-697471828,Quantitative genetics of life-history traits in a long-lived wild mammal,2000,1973-1998,"Ram Mountain, Alberta",field,female,female,66,72,NA,NA,66,72,NA,NA,163,174,parent_offspring_regression,parent_offspring_pair,no,narrow,authors,adult,adult,lifetime weaning success,reproductive success between 2 and 7 years of age,fertility,fertility,include,cor,0.54,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-697471828,table 4,fertility,fertility,family,0.604155603,66,1,0.604155603,female,adult,Mammalia,within
2077,Ovis canadensis,112,rayyan-697471828,Quantitative genetics of life-history traits in a long-lived wild mammal,2000,1973-1998,"Ram Mountain, Alberta",field,female,female,72,85,NA,NA,72,85,NA,NA,174,200,parent_offspring_regression,parent_offspring_pair,no,narrow,authors,adult,adult,reproductive success between 2 and 7 years of age,adult body mass,fertility,size,include,cor,0.46,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-697471828,table 4,fertility,size,family,0.497311288,72,1,0.497311288,female,adult,Mammalia,between
2078,Ovis canadensis,112,rayyan-697471828,Quantitative genetics of life-history traits in a long-lived wild mammal,2000,1973-1998,"Ram Mountain, Alberta",field,female,female,85,66,NA,NA,85,66,NA,NA,218,163,parent_offspring_regression,parent_offspring_pair,no,narrow,authors,both,adult,longevity,lifetime fecundity,survival,fertility,include,cor,NA,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-697471828,table 4,survival,fertility,family,NA,66,1,NA,female,cross,Mammalia,between
2079,Ovis canadensis,112,rayyan-697471828,Quantitative genetics of life-history traits in a long-lived wild mammal,2000,1973-1998,"Ram Mountain, Alberta",field,female,female,66,72,NA,NA,66,72,NA,NA,163,174,parent_offspring_regression,parent_offspring_pair,no,narrow,authors,adult,adult,lifetime weaning success,fecundity between 2 and 7 years of age,fertility,fertility,include,cor,NA,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-697471828,table 4,fertility,fertility,family,NA,66,1,NA,female,adult,Mammalia,within
2080,Ovis canadensis,112,rayyan-697471828,Quantitative genetics of life-history traits in a long-lived wild mammal,2000,1973-1998,"Ram Mountain, Alberta",field,female,female,66,66,NA,NA,66,66,NA,NA,163,163,parent_offspring_regression,parent_offspring_pair,no,narrow,authors,adult,adult,lifetime fecundity,lifetime reproductive success,fertility,fertility,include,cor,NA,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-697471828,table 4,fertility,fertility,family,NA,66,1,NA,female,adult,Mammalia,within
2081,Ovis canadensis,112,rayyan-697471828,Quantitative genetics of life-history traits in a long-lived wild mammal,2000,1973-1998,"Ram Mountain, Alberta",field,female,female,66,72,NA,NA,66,72,NA,NA,163,174,parent_offspring_regression,parent_offspring_pair,no,narrow,authors,adult,adult,lifetime fecundity,fecundity between 2 and 7 years of age,fertility,fertility,include,cor,0.98,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-697471828,table 4,fertility,fertility,family,2.297559925,66,1,2.297559925,female,adult,Mammalia,within
2082,Ovis canadensis,112,rayyan-697471828,Quantitative genetics of life-history traits in a long-lived wild mammal,2000,1973-1998,"Ram Mountain, Alberta",field,female,female,66,72,NA,NA,66,72,NA,NA,163,174,parent_offspring_regression,parent_offspring_pair,no,narrow,authors,adult,adult,lifetime fecundity,weaning success between 2 and 7 years of age,fertility,fertility,include,cor,NA,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-697471828,table 4,fertility,fertility,family,NA,66,1,NA,female,adult,Mammalia,within
2083,Ovis canadensis,112,rayyan-697471828,Quantitative genetics of life-history traits in a long-lived wild mammal,2000,1973-1998,"Ram Mountain, Alberta",field,female,female,66,72,NA,NA,66,72,NA,NA,163,174,parent_offspring_regression,parent_offspring_pair,no,narrow,authors,adult,adult,lifetime reproductive success,fecundity between 2 and 7 years of age,fertility,fertility,include,cor,NA,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-697471828,table 4,fertility,fertility,family,NA,66,1,NA,female,adult,Mammalia,within
2084,Ovis canadensis,112,rayyan-697471828,Quantitative genetics of life-history traits in a long-lived wild mammal,2000,1973-1998,"Ram Mountain, Alberta",field,female,female,66,66,NA,NA,66,66,NA,NA,175,163,parent_offspring_regression,parent_offspring_pair,no,narrow,authors,non_adult,adult,1/age at primiparity,lifetime fecundity,maturation,fertility,include,cor,0.69,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-697471828,table 4,maturation,fertility,family,0.847955755,66,1,0.847955755,female,cross,Mammalia,between
2085,Ovis canadensis,112,rayyan-697471828,Quantitative genetics of life-history traits in a long-lived wild mammal,2000,1973-1998,"Ram Mountain, Alberta",field,female,female,66,66,NA,NA,66,66,NA,NA,175,163,parent_offspring_regression,parent_offspring_pair,no,narrow,authors,non_adult,adult,1/age at primiparity,lifetime weaning success,maturation,fertility,include,cor,0.78,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-697471828,table 4,maturation,fertility,family,1.045370548,66,1,1.045370548,female,cross,Mammalia,between
2086,Ovis canadensis,112,rayyan-697471828,Quantitative genetics of life-history traits in a long-lived wild mammal,2000,1973-1998,"Ram Mountain, Alberta",field,female,female,66,66,NA,NA,66,66,NA,NA,175,163,parent_offspring_regression,parent_offspring_pair,no,narrow,authors,non_adult,adult,1/age at primiparity,lifetime reproductive success,maturation,fertility,include,cor,0.92,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-697471828,table 4,maturation,fertility,family,1.589026915,66,1,1.589026915,female,cross,Mammalia,between
2087,Ovis canadensis,112,rayyan-697471828,Quantitative genetics of life-history traits in a long-lived wild mammal,2000,1973-1998,"Ram Mountain, Alberta",field,female,female,66,66,NA,NA,66,66,NA,NA,163,163,parent_offspring_regression,parent_offspring_pair,no,narrow,authors,adult,adult,lifetime weaning success,lifetime reproductive success,fertility,fertility,include,cor,0.89,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-697471828,table 4,fertility,fertility,family,1.421925871,66,1,1.421925871,female,adult,Mammalia,within
2088,Ovis canadensis,112,rayyan-697471828,Quantitative genetics of life-history traits in a long-lived wild mammal,2000,1973-1998,"Ram Mountain, Alberta",field,female,female,72,72,NA,NA,72,72,NA,NA,174,174,parent_offspring_regression,parent_offspring_pair,no,narrow,authors,adult,adult,weaning success between 2 and 7 years of age,reproductive success between 2 and 7 years of age,fertility,fertility,include,cor,0.93,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-697471828,table 4,fertility,fertility,family,1.65839002,72,1,1.65839002,female,adult,Mammalia,within
2089,Ovis canadensis,112,rayyan-697471828,Quantitative genetics of life-history traits in a long-lived wild mammal,2000,1973-1998,"Ram Mountain, Alberta",field,female,female,72,34,NA,NA,72,34,NA,NA,174,103,parent_offspring_regression,parent_offspring_pair,no,narrow,authors,adult,adult,weaning success between 2 and 7 years of age,weaning success after 7 years of age,fertility,fertility,include,cor,0.99,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-697471828,table 4,fertility,fertility,family,2.646652412,34,1,2.646652412,female,adult,Mammalia,within
2090,Ovis canadensis,112,rayyan-697471828,Quantitative genetics of life-history traits in a long-lived wild mammal,2000,1973-1998,"Ram Mountain, Alberta",field,female,female,66,72,NA,NA,66,72,NA,NA,163,174,parent_offspring_regression,parent_offspring_pair,no,narrow,authors,adult,adult,lifetime weaning success,weaning success between 2 and 7 years of age,fertility,fertility,include,cor,0.88,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-697471828,table 4,fertility,fertility,family,1.375767657,66,1,1.375767657,female,adult,Mammalia,within
2091,Ovis canadensis,112,rayyan-697471828,Quantitative genetics of life-history traits in a long-lived wild mammal,2000,1973-1998,"Ram Mountain, Alberta",field,female,female,66,85,NA,NA,66,85,NA,NA,163,200,parent_offspring_regression,parent_offspring_pair,no,narrow,authors,adult,adult,lifetime weaning success,adult body mass,fertility,size,include,cor,0.17,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-697471828,table 4,fertility,size,family,0.171666664,66,1,0.171666664,female,adult,Mammalia,between
2092,Ovis canadensis,112,rayyan-697471828,Quantitative genetics of life-history traits in a long-lived wild mammal,2000,1973-1998,"Ram Mountain, Alberta",field,female,female,85,66,NA,NA,85,66,NA,NA,218,175,parent_offspring_regression,parent_offspring_pair,no,narrow,authors,both,non_adult,longevity,1/age at primiparity,survival,maturation,include,cor,0.32,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-697471828,table 4,survival,maturation,family,0.331647109,66,1,0.331647109,female,cross,Mammalia,between
2093,Ovis canadensis,112,rayyan-697471828,Quantitative genetics of life-history traits in a long-lived wild mammal,2000,1973-1998,"Ram Mountain, Alberta",field,female,female,85,66,NA,NA,85,66,NA,NA,218,163,parent_offspring_regression,parent_offspring_pair,no,narrow,authors,both,adult,longevity,lifetime reproductive success,survival,fertility,include,cor,NA,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-697471828,table 4,survival,fertility,family,NA,66,1,NA,female,cross,Mammalia,between
2094,Ovis canadensis,112,rayyan-697471828,Quantitative genetics of life-history traits in a long-lived wild mammal,2000,1973-1998,"Ram Mountain, Alberta",field,female,female,85,72,NA,NA,85,72,NA,NA,218,174,parent_offspring_regression,parent_offspring_pair,no,narrow,authors,both,adult,longevity,weaning success between 2 and 7 years of age,survival,fertility,include,cor,NA,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-697471828,table 4,survival,fertility,family,NA,72,1,NA,female,cross,Mammalia,between
2095,Ovis canadensis,112,rayyan-697471828,Quantitative genetics of life-history traits in a long-lived wild mammal,2000,1973-1998,"Ram Mountain, Alberta",field,female,female,85,72,NA,NA,85,72,NA,NA,218,174,parent_offspring_regression,parent_offspring_pair,no,narrow,authors,both,adult,longevity,fecundity between 2 and 7 years of age,survival,fertility,include,cor,0.69,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-697471828,table 4,survival,fertility,family,0.847955755,72,1,0.847955755,female,cross,Mammalia,between
2096,Ovis canadensis,112,rayyan-697471828,Quantitative genetics of life-history traits in a long-lived wild mammal,2000,1973-1998,"Ram Mountain, Alberta",field,female,female,85,34,NA,NA,85,34,NA,NA,218,103,parent_offspring_regression,parent_offspring_pair,no,narrow,authors,both,adult,longevity,weaning success after 7 years of age,survival,fertility,include,cor,NA,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-697471828,table 4,survival,fertility,family,NA,34,1,NA,female,cross,Mammalia,between
2097,Ovis canadensis,393,rayyan-697472982,Selection and genetic (co)variance in bighorn sheep,2005,1971-2002,"Ram Mountain, Alberta, Canada",field,female,female,NA,NA,NA,NA,NA,NA,NA,NA,287,240,animal_model,pedigree,no,narrow,authors,adult,adult,female weight in june,Female fecundity,size,fertility,include,cor,0.59,0.15,se,NA,NA,NA,NA,NA,NA,rayyan-697472982,table 4,size,fertility,pedigree,0.677666068,240,1,0.677666068,female,adult,Mammalia,between
2098,Ovis canadensis,112,rayyan-697471828,Quantitative genetics of life-history traits in a long-lived wild mammal,2000,1973-1998,"Ram Mountain, Alberta",field,female,female,72,72,NA,NA,72,72,NA,NA,174,174,parent_offspring_regression,parent_offspring_pair,no,narrow,authors,adult,adult,fecundity between 2 and 7 years of age,reproductive success between 2 and 7 years of age,fertility,fertility,include,cor,NA,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-697471828,table 4,fertility,fertility,family,NA,72,1,NA,female,adult,Mammalia,within
2099,Ovis canadensis,112,rayyan-697471828,Quantitative genetics of life-history traits in a long-lived wild mammal,2000,1973-1998,"Ram Mountain, Alberta",field,female,female,85,85,NA,NA,85,85,NA,NA,218,200,parent_offspring_regression,parent_offspring_pair,no,narrow,authors,both,adult,longevity,adult body mass,survival,size,include,cor,0.34,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-697471828,table 4,survival,size,family,0.354092529,85,1,0.354092529,female,cross,Mammalia,between
2100,Ovis canadensis,112,rayyan-697471828,Quantitative genetics of life-history traits in a long-lived wild mammal,2000,1973-1998,"Ram Mountain, Alberta",field,female,female,72,85,NA,NA,72,85,NA,NA,174,200,parent_offspring_regression,parent_offspring_pair,no,narrow,authors,adult,adult,fecundity between 2 and 7 years of age,adult body mass,fertility,size,include,cor,-0.34,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-697471828,table 4,fertility,size,family,-0.354092529,72,1,-0.354092529,female,adult,Mammalia,between
2101,Ovis canadensis,112,rayyan-697471828,Quantitative genetics of life-history traits in a long-lived wild mammal,2000,1973-1998,"Ram Mountain, Alberta",field,female,female,72,85,NA,NA,72,85,NA,NA,174,200,parent_offspring_regression,parent_offspring_pair,no,narrow,authors,adult,adult,weaning success between 2 and 7 years of age,adult body mass,fertility,size,include,cor,0.24,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-697471828,table 4,fertility,size,family,0.244774113,72,1,0.244774113,female,adult,Mammalia,between
2102,Ovis canadensis,112,rayyan-697471828,Quantitative genetics of life-history traits in a long-lived wild mammal,2000,1973-1998,"Ram Mountain, Alberta",field,female,female,34,85,NA,NA,34,85,NA,NA,103,200,parent_offspring_regression,parent_offspring_pair,no,narrow,authors,adult,adult,weaning success after 7 years of age,adult body mass,fertility,size,include,cor,0.51,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-697471828,table 4,fertility,size,family,0.562729769,34,1,0.562729769,female,adult,Mammalia,between
2103,Ovis canadensis,393,rayyan-697472982,Selection and genetic (co)variance in bighorn sheep,2005,1971-2002,"Ram Mountain, Alberta, Canada",field,female,female,NA,NA,NA,NA,NA,NA,NA,NA,180,240,animal_model,pedigree,no,narrow,authors,non_adult,adult,female lamb weight in Sept,Female fecundity,size,fertility,include,cor,0.38,0.14,se,NA,NA,NA,NA,NA,NA,rayyan-697472982,table 4,size,fertility,pedigree,0.40005965,180,1,0.40005965,female,cross,Mammalia,between
2104,Ovis canadensis,112,rayyan-697471828,Quantitative genetics of life-history traits in a long-lived wild mammal,2000,1973-1998,"Ram Mountain, Alberta",field,female,female,72,34,NA,NA,72,34,NA,NA,174,103,parent_offspring_regression,parent_offspring_pair,no,narrow,authors,adult,adult,reproductive success between 2 and 7 years of age,weaning success after 7 years of age,fertility,fertility,include,cor,0.61,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-697471828,table 4,fertility,fertility,family,0.708921359,34,1,0.708921359,female,adult,Mammalia,within
2105,Ovis canadensis,112,rayyan-697471828,Quantitative genetics of life-history traits in a long-lived wild mammal,2000,1973-1998,"Ram Mountain, Alberta",field,female,female,66,34,NA,NA,66,34,NA,NA,163,103,parent_offspring_regression,parent_offspring_pair,no,narrow,authors,adult,adult,lifetime reproductive success,weaning success after 7 years of age,fertility,fertility,include,cor,0.98,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-697471828,table 4,fertility,fertility,family,2.297559925,34,1,2.297559925,female,adult,Mammalia,within
2106,Ovis canadensis,112,rayyan-697471828,Quantitative genetics of life-history traits in a long-lived wild mammal,2000,1973-1998,"Ram Mountain, Alberta",field,female,female,72,72,NA,NA,72,72,NA,NA,174,174,parent_offspring_regression,parent_offspring_pair,no,narrow,authors,adult,adult,fecundity between 2 and 7 years of age,weaning success between 2 and 7 years of age,fertility,fertility,include,cor,0.99,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-697471828,table 4,fertility,fertility,family,2.646652412,72,1,2.646652412,female,adult,Mammalia,within
2107,Ovis canadensis,112,rayyan-697471828,Quantitative genetics of life-history traits in a long-lived wild mammal,2000,1973-1998,"Ram Mountain, Alberta",field,female,female,66,72,NA,NA,66,72,NA,NA,163,174,parent_offspring_regression,parent_offspring_pair,no,narrow,authors,adult,adult,lifetime fecundity,reproductive success between 2 and 7 years of age,fertility,fertility,include,cor,0.77,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-697471828,table 4,fertility,fertility,family,1.020327758,66,1,1.020327758,female,adult,Mammalia,within
2108,Ovis canadensis,112,rayyan-697471828,Quantitative genetics of life-history traits in a long-lived wild mammal,2000,1973-1998,"Ram Mountain, Alberta",field,female,female,85,66,NA,NA,85,66,NA,NA,218,163,parent_offspring_regression,parent_offspring_pair,no,narrow,authors,both,adult,longevity,lifetime weaning success,survival,fertility,include,cor,NA,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-697471828,table 4,survival,fertility,family,NA,66,1,NA,female,cross,Mammalia,between
2109,Ovis canadensis,112,rayyan-697471828,Quantitative genetics of life-history traits in a long-lived wild mammal,2000,1973-1998,"Ram Mountain, Alberta",field,female,female,66,85,NA,NA,66,85,NA,NA,163,200,parent_offspring_regression,parent_offspring_pair,no,narrow,authors,adult,adult,lifetime fecundity,adult body mass,fertility,size,include,cor,-8.00E-04,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-697471828,table 4,fertility,size,family,-0.0008,66,1,-0.0008,female,adult,Mammalia,between
2110,Ovis canadensis,393,rayyan-697472982,Selection and genetic (co)variance in bighorn sheep,2005,1971-2002,"Ram Mountain, Alberta, Canada",field,female,female,NA,NA,NA,NA,NA,NA,NA,NA,276,240,animal_model,pedigree,no,narrow,authors,adult,adult,female weight in sept,Female fecundity,size,fertility,include,cor,0.45,0.14,se,NA,NA,NA,NA,NA,NA,rayyan-697472982,table 4,size,fertility,pedigree,0.484700279,240,1,0.484700279,female,adult,Mammalia,between
2111,Ovis canadensis,112,rayyan-697471828,Quantitative genetics of life-history traits in a long-lived wild mammal,2000,1973-1998,"Ram Mountain, Alberta",field,female,female,72,34,NA,NA,72,34,NA,NA,174,103,parent_offspring_regression,parent_offspring_pair,no,narrow,authors,adult,adult,fecundity between 2 and 7 years of age,weaning success after 7 years of age,fertility,fertility,include,cor,NA,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-697471828,table 4,fertility,fertility,family,NA,34,1,NA,female,adult,Mammalia,within
2112,Ovis canadensis,112,rayyan-697471828,Quantitative genetics of life-history traits in a long-lived wild mammal,2000,1973-1998,"Ram Mountain, Alberta",field,female,female,66,72,NA,NA,66,72,NA,NA,163,174,parent_offspring_regression,parent_offspring_pair,no,narrow,authors,adult,adult,lifetime reproductive success,reproductive success between 2 and 7 years of age,fertility,fertility,include,cor,0.81,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-697471828,table 4,fertility,fertility,family,1.127029026,66,1,1.127029026,female,adult,Mammalia,within
2113,Ovis canadensis,112,rayyan-697471828,Quantitative genetics of life-history traits in a long-lived wild mammal,2000,1973-1998,"Ram Mountain, Alberta",field,female,female,66,72,NA,NA,66,72,NA,NA,163,174,parent_offspring_regression,parent_offspring_pair,no,narrow,authors,adult,adult,lifetime reproductive success,weaning success between 2 and 7 years of age,fertility,fertility,include,cor,0.92,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-697471828,table 4,fertility,fertility,family,1.589026915,66,1,1.589026915,female,adult,Mammalia,within
2114,Ovis canadensis,112,rayyan-697471828,Quantitative genetics of life-history traits in a long-lived wild mammal,2000,1973-1998,"Ram Mountain, Alberta",field,female,female,66,34,NA,NA,66,34,NA,NA,163,103,parent_offspring_regression,parent_offspring_pair,no,narrow,authors,adult,adult,lifetime fecundity,weaning success after 7 years of age,fertility,fertility,include,cor,NA,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-697471828,table 4,fertility,fertility,family,NA,34,1,NA,female,adult,Mammalia,within
2115,Ovis canadensis,112,rayyan-697471828,Quantitative genetics of life-history traits in a long-lived wild mammal,2000,1973-1998,"Ram Mountain, Alberta",field,female,female,66,85,NA,NA,66,85,NA,NA,163,200,parent_offspring_regression,parent_offspring_pair,no,narrow,authors,adult,adult,lifetime reproductive success,adult body mass,fertility,size,include,cor,0.25,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-697471828,table 4,fertility,size,family,0.255412812,66,1,0.255412812,female,adult,Mammalia,between
2116,Ovis canadensis,393,rayyan-697472982,Selection and genetic (co)variance in bighorn sheep,2005,1971-2002,"Ram Mountain, Alberta, Canada",field,female,female,NA,NA,NA,NA,NA,NA,NA,NA,174,240,animal_model,pedigree,no,narrow,authors,non_adult,adult,female lamb weight in June,Female fecundity,size,fertility,include,cor,0.22,0.2,se,NA,NA,NA,NA,NA,NA,rayyan-697472982,table 4,size,fertility,pedigree,0.223656109,174,1,0.223656109,female,cross,Mammalia,between
2117,Panorpa cognata,212,rayyan-197247282,Environment-dependent genetic correlations between development time and body mass in a scorpionfly,2007,2002,Freiburg i.Br. in south-western Germany,lab,both,both,27,27,NA,NA,27,27,27,27,NA,NA,family_mean_correlation,full_sib,no,broad,authors,non_adult,non_adult,development time,body growth,reverse_maturation,growth,include,cor,0.057,0.13,se,NA,NA,NA,NA,NA,NA,high,gentic correlations between traits,maturation,growth,family,0.057061852,27,-1,-0.057061852,both,non_adult,Insecta,between
2118,Panorpa cognata,212,rayyan-197247282,Environment-dependent genetic correlations between development time and body mass in a scorpionfly,2007,2002,Freiburg i.Br. in south-western Germany,lab,both,both,27,27,NA,NA,27,27,27,27,NA,NA,family_mean_correlation,full_sib,no,broad,authors,non_adult,non_adult,development time,body growth,reverse_maturation,growth,include,cor,-0.293,0.087,se,NA,NA,NA,NA,NA,NA,low,gentic correlations between traits,maturation,growth,family,-0.301844856,27,-1,0.301844856,both,non_adult,Insecta,between
2119,Parnara guttata guttata,291,rayyan-197247828,"Genetic and environmental sources of egg size, fecundity and body size in the migrant skipper, Parnara guttata guttata( Lepidoptera : Hesperiidae)",2006,2000,"Okayama, Honshu, Japan",lab,both,both,10,10,NA,NA,10,10,10,10,49,49,family_mean_correlation,full_sib,no,broad,CC,adult,non_adult,forewing length,egg size,size,size,include,cor,-0.587,NA,NA,NA,NA,NA,NA,NA,NA,family_mean_14l_25c,table 3,size,size,family,-0.673076564,10,1,-0.673076564,both,cross,Insecta,within
2120,Parnara guttata guttata,291,rayyan-197247828,"Genetic and environmental sources of egg size, fecundity and body size in the migrant skipper, Parnara guttata guttata( Lepidoptera : Hesperiidae)",2006,2000,"Okayama, Honshu, Japan",lab,both,female,10,10,NA,NA,10,10,10,10,49,49,family_mean_correlation,full_sib,no,broad,CC,non_adult,adult,egg size,fecundity,size,fertility,include,cor,-0.672,NA,NA,NA,NA,NA,NA,NA,NA,family_mean_14l_25c,table 3,size,fertility,family,-0.814381093,10,1,-0.814381093,female,cross,Insecta,between
2121,Parnara guttata guttata,291,rayyan-197247828,"Genetic and environmental sources of egg size, fecundity and body size in the migrant skipper, Parnara guttata guttata( Lepidoptera : Hesperiidae)",2006,2000,"Okayama, Honshu, Japan",lab,both,female,24,24,NA,NA,24,24,24,24,215,215,parent_offspring_regression,full_sib,no,broad,CC,non_adult,adult,egg size,fecundity,size,fertility,include,cor,-0.96,NA,NA,NA,NA,NA,NA,NA,NA,parent-offspring_regression_16l_25c,table 3,size,fertility,family,-1.945910149,24,1,-1.945910149,female,cross,Insecta,between
2122,Parnara guttata guttata,291,rayyan-197247828,"Genetic and environmental sources of egg size, fecundity and body size in the migrant skipper, Parnara guttata guttata( Lepidoptera : Hesperiidae)",2006,2000,"Okayama, Honshu, Japan",lab,both,both,9,9,NA,NA,9,9,9,9,63,63,family_mean_correlation,full_sib,no,broad,CC,adult,non_adult,forewing length,egg size,size,size,include,cor,0.1,NA,NA,NA,NA,NA,NA,NA,NA,family_mean_16l_20c,table 3,size,size,family,0.100335348,9,1,0.100335348,both,cross,Insecta,within
2123,Parnara guttata guttata,291,rayyan-197247828,"Genetic and environmental sources of egg size, fecundity and body size in the migrant skipper, Parnara guttata guttata( Lepidoptera : Hesperiidae)",2006,2000,"Okayama, Honshu, Japan",lab,both,female,24,24,NA,NA,24,24,24,24,215,215,parent_offspring_regression,full_sib,no,broad,CC,adult,adult,forewing length,fecundity,size,fertility,include,cor,-0.17,NA,NA,NA,NA,NA,NA,NA,NA,parent-offspring_regression_16l_25c,table 3,size,fertility,family,-0.171666664,24,1,-0.171666664,female,adult,Insecta,between
2125,Parnara guttata guttata,291,rayyan-197247828,"Genetic and environmental sources of egg size, fecundity and body size in the migrant skipper, Parnara guttata guttata( Lepidoptera : Hesperiidae)",2006,2000,"Okayama, Honshu, Japan",lab,both,both,24,24,NA,NA,24,24,24,24,215,215,parent_offspring_regression,full_sib,no,broad,CC,adult,non_adult,forewing length,egg size,size,size,include,cor,0.19,NA,NA,NA,NA,NA,NA,NA,NA,parent-offspring_regression_16l_25c,table 3,size,size,family,0.192337169,24,1,0.192337169,both,cross,Insecta,within
2126,Parnara guttata guttata,291,rayyan-197247828,"Genetic and environmental sources of egg size, fecundity and body size in the migrant skipper, Parnara guttata guttata( Lepidoptera : Hesperiidae)",2006,2000,"Okayama, Honshu, Japan",lab,both,female,10,10,NA,NA,10,10,10,10,49,49,family_mean_correlation,full_sib,no,broad,CC,adult,adult,forewing length,fecundity,size,fertility,include,cor,0.638,NA,NA,NA,NA,NA,NA,NA,NA,family_mean_14l_25c,table 3,size,fertility,family,0.754793526,10,1,0.754793526,female,adult,Insecta,between
2128,Parnara guttata guttata,291,rayyan-197247828,"Genetic and environmental sources of egg size, fecundity and body size in the migrant skipper, Parnara guttata guttata( Lepidoptera : Hesperiidae)",2006,2000,"Okayama, Honshu, Japan",lab,both,female,9,9,NA,NA,9,9,9,9,63,63,family_mean_correlation,full_sib,no,broad,CC,adult,adult,forewing length,fecundity,size,fertility,include,cor,-0.532,NA,NA,NA,NA,NA,NA,NA,NA,family_mean_16l_20c,table 3,size,fertility,family,-0.592930527,9,1,-0.592930527,female,adult,Insecta,between
2129,Parnara guttata guttata,291,rayyan-197247828,"Genetic and environmental sources of egg size, fecundity and body size in the migrant skipper, Parnara guttata guttata( Lepidoptera : Hesperiidae)",2006,2000,"Okayama, Honshu, Japan",lab,both,female,9,9,NA,NA,9,9,9,9,63,63,family_mean_correlation,full_sib,no,broad,CC,non_adult,adult,egg size,fecundity,size,fertility,include,cor,-0.201,NA,NA,NA,NA,NA,NA,NA,NA,family_mean_16l_20c,table 3,size,fertility,family,-0.203774438,9,1,-0.203774438,female,cross,Insecta,between
2149,Parus major,328,rayyan-697472542,Testing for biases in selection on avian reproductive traits and partitioning direct and indirect selection using quantitative genetic models,2016,1955-2013,"Hoge Veluwe, Netherlands",field,female,female,NA,NA,NA,NA,NA,NA,NA,NA,2871,2871,animal_model,pedigree,yes,narrow,authors,adult,adult,Clutch size,Number of recruits,fertility,fertility,include,cor,0.18,"[-0.13, 0.50]",95CI,NA,NA,NA,NA,NA,NA,Hoge_Veluwe_all_years,table s1,fertility,fertility,pedigree,0.181982689,2871,1,0.181982689,female,adult,Aves,within
2157,Parus major,328,rayyan-697472542,Testing for biases in selection on avian reproductive traits and partitioning direct and indirect selection using quantitative genetic models,2016,1955-2013,"Hoge Veluwe, Netherlands",field,female,female,NA,NA,NA,NA,NA,NA,NA,NA,1663,1663,animal_model,pedigree,yes,narrow,authors,adult,adult,Clutch size,Number of recruits,fertility,fertility,include,cor,-0.03," [-0.3, 0.32]",95CI,NA,NA,NA,NA,NA,NA,Vlieland_East_all_years,table s1,fertility,fertility,pedigree,-0.030009005,1663,1,-0.030009005,female,adult,Aves,within
2170,Parus major,345,rayyan-697472698,Genomic dissection of variation in clutch size and egg mass in a wild great tit (Parus major) population,2013,1958-2011,"Oxford, United Kingdom",field,female,both,NA,NA,NA,NA,NA,NA,NA,NA,635,635,animal_model,pedigree,no,narrow,authors,adult,non_adult,clutch size,egg mass,fertility,size,include,cor,-0.12,0.089,se,NA,NA,NA,NA,NA,NA,rayyan-697472698,table 3,fertility,size,pedigree,-0.120581028,635,1,-0.120581028,female,cross,Aves,between
2179,Passer domesticus,189,rayyan-197247171,Maternal effects and heritability of annual productivity,2012,2000-2008,"Lundy Island, Bristol, UK",field,both,both,NA,NA,NA,NA,NA,NA,NA,NA,609,609,animal_model,pedigree,no,narrow,authors,adult,both,annual productivity,longevity,fertility,survival,include,cor,-0.03,"[-0.008, 0.001]",95CI,NA,NA,NA,NA,NA,NA,rayyan-197247171,first para in quantitative genetic analysis,fertility,survival,pedigree,-0.030009005,609,1,-0.030009005,both,cross,Aves,between
2180,Pholcus phalangioides,102,rayyan-697471783,Food and sex-specific growth strategies in a spider,2004,2001,"Bonn, Germany",lab,male,male,39,39,NA,NA,39,39,39,39,296,296,animal_model,full_sib,no,broad,authors,adult,non_adult,adult body size,development time ,size,reverse_maturation,include,cor,0.7,0.05,se,NA,NA,NA,NA,NA,NA,low_food_male,2nd para of phenotypic and genetic correlation,size,maturation,family,0.867300528,39,-1,-0.867300528,male,cross,Arachnida,between
2181,Pholcus phalangioides,102,rayyan-697471783,Food and sex-specific growth strategies in a spider,2004,2001,"Bonn, Germany",lab,female,female,39,39,NA,NA,39,39,39,39,286,286,animal_model,full_sib,no,broad,authors,adult,non_adult,adult body size,development time ,size,reverse_maturation,include,cor,0.49,0.09,se,NA,NA,NA,NA,NA,NA,low_food_female,2nd para of phenotypic and genetic correlation,size,maturation,family,0.536060337,39,-1,-0.536060337,female,cross,Arachnida,between
2182,Pholcus phalangioides,102,rayyan-697471783,Food and sex-specific growth strategies in a spider,2004,2001,"Bonn, Germany",lab,male,male,39,39,NA,NA,39,39,39,39,285,285,animal_model,full_sib,no,broad,authors,adult,non_adult,adult body size,development time ,size,reverse_maturation,include,cor,0.16,0.1,se,NA,NA,NA,NA,NA,NA,high_food_male,2nd para of phenotypic and genetic correlation,size,maturation,family,0.161386696,39,-1,-0.161386696,male,cross,Arachnida,between
2183,Pholcus phalangioides,102,rayyan-697471783,Food and sex-specific growth strategies in a spider,2004,2001,"Bonn, Germany",lab,female,female,39,39,NA,NA,39,39,39,39,297,297,animal_model,full_sib,no,broad,authors,adult,non_adult,adult body size,development time ,size,reverse_maturation,include,cor,0.03,0.11,se,NA,NA,NA,NA,NA,NA,high_food_female,2nd para of phenotypic and genetic correlation,size,maturation,family,0.030009005,39,-1,-0.030009005,female,cross,Arachnida,between
2184,Physa acuta,370,rayyan-697472843,The effects of predation risk on mating system expression in a freshwater snail,2010,2007,"PA, USA",lab,both,both,30,30,NA,NA,30,30,30,30,150,150,animal_model,full_sib,no,broad,authors,adult,adult,growth rate,size at first reproduction ,growth,size,include,cor,0.28,NA,NA,NA,NA,NA,NA,NA,NA,no_predator_mate_unavailable,table 3,growth,size,family,0.287682072,30,1,0.287682072,both,adult,Gastropoda,between
2185,Physa acuta,370,rayyan-697472843,The effects of predation risk on mating system expression in a freshwater snail,2010,2007,"PA, USA",lab,both,both,30,30,NA,NA,30,30,30,30,210,210,animal_model,full_sib,no,broad,authors,adult,non_adult,growth rate,early survival (proportion of eggs that hatched and survived),growth,survival,include,cor,0.09,NA,NA,NA,NA,NA,NA,NA,NA,predator_mate_available,table 3,growth,survival,family,0.090244188,30,1,0.090244188,both,cross,Gastropoda,between
2186,Physa acuta,370,rayyan-697472843,The effects of predation risk on mating system expression in a freshwater snail,2010,2007,"PA, USA",lab,both,both,30,30,NA,NA,30,30,30,30,210,210,animal_model,full_sib,no,broad,authors,adult,non_adult,growth rate,age at first reproduction,growth,reverse_maturation,include,cor,-0.15,NA,NA,NA,NA,NA,NA,NA,NA,predator_mate_available,table 3,growth,maturation,family,-0.151140436,30,-1,0.151140436,both,cross,Gastropoda,between
2187,Physa acuta,370,rayyan-697472843,The effects of predation risk on mating system expression in a freshwater snail,2010,2007,"PA, USA",lab,both,both,30,30,NA,NA,30,30,30,30,210,210,animal_model,full_sib,no,broad,authors,non_adult,non_adult,age at first reproduction,early survival (proportion of eggs that hatched and survived),reverse_maturation,survival,include,cor,-0.32,NA,NA,NA,NA,NA,NA,NA,NA,predator_mate_available,table 3,maturation,survival,family,-0.331647109,30,-1,0.331647109,both,non_adult,Gastropoda,between
2188,Physa acuta,370,rayyan-697472843,The effects of predation risk on mating system expression in a freshwater snail,2010,2007,"PA, USA",lab,both,both,30,30,NA,NA,30,30,30,30,210,210,animal_model,full_sib,no,broad,authors,adult,adult,growth rate,size at first reproduction ,growth,size,include,cor,0.54,NA,NA,NA,NA,NA,NA,NA,NA,no_predator_mate_available,table 3,growth,size,family,0.604155603,30,1,0.604155603,both,adult,Gastropoda,between
2189,Physa acuta,370,rayyan-697472843,The effects of predation risk on mating system expression in a freshwater snail,2010,2007,"PA, USA",lab,both,both,30,30,NA,NA,30,30,30,30,210,210,animal_model,full_sib,no,broad,authors,adult,non_adult,size at first reproduction ,early survival (proportion of eggs that hatched and survived),size,survival,include,cor,0.14,NA,NA,NA,NA,NA,NA,NA,NA,predator_mate_available,table 3,size,survival,family,0.140925576,30,1,0.140925576,both,cross,Gastropoda,between
2190,Physa acuta,370,rayyan-697472843,The effects of predation risk on mating system expression in a freshwater snail,2010,2007,"PA, USA",lab,both,both,30,30,NA,NA,30,30,30,30,210,210,animal_model,full_sib,no,broad,authors,non_adult,adult,age at first reproduction,size at first reproduction ,reverse_maturation,size,include,cor,-0.049,NA,NA,NA,NA,NA,NA,NA,NA,predator_mate_available,table 3,maturation,size,family,-0.049039273,30,-1,0.049039273,both,cross,Gastropoda,between
2191,Physa acuta,370,rayyan-697472843,The effects of predation risk on mating system expression in a freshwater snail,2010,2007,"PA, USA",lab,both,both,30,30,NA,NA,30,30,30,30,150,150,animal_model,full_sib,no,broad,authors,adult,non_adult,growth rate,age at first reproduction,growth,reverse_maturation,include,cor,0.24,NA,NA,NA,NA,NA,NA,NA,NA,predator_mate_unavailable,table 3,growth,maturation,family,0.244774113,30,-1,-0.244774113,both,cross,Gastropoda,between
2192,Physa acuta,370,rayyan-697472843,The effects of predation risk on mating system expression in a freshwater snail,2010,2007,"PA, USA",lab,both,both,30,30,NA,NA,30,30,30,30,150,150,animal_model,full_sib,no,broad,authors,non_adult,adult,age at first reproduction,size at first reproduction ,reverse_maturation,size,include,cor,0.47,NA,NA,NA,NA,NA,NA,NA,NA,no_predator_mate_unavailable,table 3,maturation,size,family,0.510070337,30,-1,-0.510070337,both,cross,Gastropoda,between
2193,Physa acuta,370,rayyan-697472843,The effects of predation risk on mating system expression in a freshwater snail,2010,2007,"PA, USA",lab,both,both,30,30,NA,NA,30,30,30,30,150,150,animal_model,full_sib,no,broad,authors,adult,non_adult,growth rate,age at first reproduction,growth,reverse_maturation,include,cor,0.06,NA,NA,NA,NA,NA,NA,NA,NA,no_predator_mate_unavailable,table 3,growth,maturation,family,0.060072156,30,-1,-0.060072156,both,cross,Gastropoda,between
2194,Physa acuta,370,rayyan-697472843,The effects of predation risk on mating system expression in a freshwater snail,2010,2007,"PA, USA",lab,both,both,30,30,NA,NA,30,30,30,30,210,210,animal_model,full_sib,no,broad,authors,adult,adult,growth rate,size at first reproduction ,growth,size,include,cor,0.43,NA,NA,NA,NA,NA,NA,NA,NA,predator_mate_available,table 3,growth,size,family,0.459896681,30,1,0.459896681,both,adult,Gastropoda,between
2195,Physa acuta,370,rayyan-697472843,The effects of predation risk on mating system expression in a freshwater snail,2010,2007,"PA, USA",lab,both,both,30,30,NA,NA,30,30,30,30,150,150,animal_model,full_sib,no,broad,authors,non_adult,adult,age at first reproduction,size at first reproduction ,reverse_maturation,size,include,cor,0.32,NA,NA,NA,NA,NA,NA,NA,NA,predator_mate_unavailable,table 3,maturation,size,family,0.331647109,30,-1,-0.331647109,both,cross,Gastropoda,between
2196,Physa acuta,370,rayyan-697472843,The effects of predation risk on mating system expression in a freshwater snail,2010,2007,"PA, USA",lab,both,both,30,30,NA,NA,30,30,30,30,150,150,animal_model,full_sib,no,broad,authors,adult,adult,growth rate,size at first reproduction ,growth,size,include,cor,0.23,NA,NA,NA,NA,NA,NA,NA,NA,predator_mate_unavailable,table 3,growth,size,family,0.234189467,30,1,0.234189467,both,adult,Gastropoda,between
2197,Physa acuta,370,rayyan-697472843,The effects of predation risk on mating system expression in a freshwater snail,2010,2007,"PA, USA",lab,both,both,30,30,NA,NA,30,30,30,30,150,150,animal_model,full_sib,no,broad,authors,non_adult,non_adult,age at first reproduction,early survival (proportion of eggs that hatched and survived),reverse_maturation,survival,include,cor,NA,NA,NA,NA,NA,NA,NA,NA,NA,predator_mate_unavailable,table 3,maturation,survival,family,NA,30,-1,NA,both,non_adult,Gastropoda,between
2198,Physa acuta,370,rayyan-697472843,The effects of predation risk on mating system expression in a freshwater snail,2010,2007,"PA, USA",lab,both,both,30,30,NA,NA,30,30,30,30,150,150,animal_model,full_sib,no,broad,authors,adult,non_adult,size at first reproduction ,early survival (proportion of eggs that hatched and survived),size,survival,include,cor,NA,NA,NA,NA,NA,NA,NA,NA,NA,predator_mate_unavailable,table 3,size,survival,family,NA,30,1,NA,both,cross,Gastropoda,between
2199,Physa acuta,370,rayyan-697472843,The effects of predation risk on mating system expression in a freshwater snail,2010,2007,"PA, USA",lab,both,both,30,30,NA,NA,30,30,30,30,150,150,animal_model,full_sib,no,broad,authors,adult,non_adult,growth rate,early survival (proportion of eggs that hatched and survived),growth,survival,include,cor,-0.57,NA,NA,NA,NA,NA,NA,NA,NA,predator_mate_unavailable,table 3,growth,survival,family,-0.647522845,30,1,-0.647522845,both,cross,Gastropoda,between
2200,Plodia interpunctella,366,rayyan-697472822,"Evidence for strong intralocus sexual conflict in the indian meal moth, plodia interpunctella",2011,2001,"Perth, Australia",lab,female,female,NA,NA,NA,NA,75,75,25,25,225,225,animal_model,half_sib,no,narrow,authors,non_adult,both,development time,(adult) longevity,reverse_maturation,survival,include,cov,-0.993329154,NA,NA,0.57,NA,NA,0.233,NA,NA,female,table 4,maturation,survival,family,-2.849907399,75,-1,2.849907399,female,cross,Insecta,between
2201,Plodia interpunctella,366,rayyan-697472822,"Evidence for strong intralocus sexual conflict in the indian meal moth, plodia interpunctella",2011,2001,"Perth, Australia",lab,female,female,NA,NA,NA,NA,75,75,25,25,225,225,animal_model,half_sib,no,narrow,authors,non_adult,adult,development time,adult size,reverse_maturation,size,include,cov,0.349982911,NA,NA,0.57,NA,NA,0.033,NA,NA,female,table 4,maturation,size,family,0.36542428,75,-1,-0.36542428,female,cross,Insecta,between
2202,Plodia interpunctella,366,rayyan-697472822,"Evidence for strong intralocus sexual conflict in the indian meal moth, plodia interpunctella",2011,2001,"Perth, Australia",lab,female,female,NA,NA,NA,NA,75,75,25,25,225,225,animal_model,half_sib,no,narrow,authors,both,adult,(adult) longevity,adult size,survival,size,include,cov,-0.399147225,NA,NA,0.233,NA,NA,0.033,NA,NA,female,table 4,survival,size,family,-0.422634133,75,1,-0.422634133,female,cross,Insecta,between
2203,Plodia interpunctella,366,rayyan-697472822,"Evidence for strong intralocus sexual conflict in the indian meal moth, plodia interpunctella",2011,2001,"Perth, Australia",lab,male,male,NA,NA,NA,NA,75,75,25,25,225,225,animal_model,half_sib,no,narrow,authors,non_adult,adult,development time,adult size,reverse_maturation,size,include,cov,0.859086731,NA,NA,4.736,NA,NA,0.661,NA,NA,male,table 4,maturation,size,family,1.289848028,75,-1,-1.289848028,male,cross,Insecta,between
2204,Plodia interpunctella,366,rayyan-697472822,"Evidence for strong intralocus sexual conflict in the indian meal moth, plodia interpunctella",2011,2001,"Perth, Australia",lab,male,male,NA,NA,NA,NA,75,75,25,25,225,225,animal_model,half_sib,no,narrow,authors,non_adult,both,development time,(adult) longevity,reverse_maturation,survival,include,cov,0.043062303,NA,NA,4.736,NA,NA,0.124,NA,NA,male,table 4,maturation,survival,family,0.04308895,75,-1,-0.04308895,male,cross,Insecta,between
2205,Plodia interpunctella,366,rayyan-697472822,"Evidence for strong intralocus sexual conflict in the indian meal moth, plodia interpunctella",2011,2001,"Perth, Australia",lab,male,male,NA,NA,NA,NA,75,75,25,25,225,225,animal_model,half_sib,no,narrow,authors,both,adult,(adult) longevity,adult size,survival,size,include,cov,0.548388173,NA,NA,0.124,NA,NA,0.661,NA,NA,male,table 4,survival,size,family,0.61607338,75,1,0.61607338,male,cross,Insecta,between
2206,Priophorus pallipes,26,rayyan-687940492,Seasonality and genetic architecture of development time and body size of the birch feeding sawfly Priophorus pallipes,2001,1998,"Kevo Subarctic Research Institute, Finland",lab,male,male,NA,NA,60,60,60,60,0,0,596,596,animal_model,genetic_line,no,broad,authors,non_adult,non_adult,development time (number of days from the beginnig of the experiment to the cessation of feeding),final larval mass,reverse_maturation,size,include,cor,-0.27,NA,NA,NA,NA,NA,NA,NA,NA,decline,figure 2,maturation,size,genotype,-0.276863823,60,-1,0.276863823,male,non_adult,Insecta,between
2207,Priophorus pallipes,26,rayyan-687940492,Seasonality and genetic architecture of development time and body size of the birch feeding sawfly Priophorus pallipes,2001,1998,"Kevo Subarctic Research Institute, Finland",lab,male,male,NA,NA,60,60,60,60,0,0,594,594,animal_model,genetic_line,no,broad,authors,non_adult,non_adult,development time (number of days from the beginnig of the experiment to the cessation of feeding),final larval mass,reverse_maturation,size,include,cor,-0.59,NA,NA,NA,NA,NA,NA,NA,NA,low,figure 2,maturation,size,genotype,-0.677666068,60,-1,0.677666068,male,non_adult,Insecta,between
2208,Priophorus pallipes,26,rayyan-687940492,Seasonality and genetic architecture of development time and body size of the birch feeding sawfly Priophorus pallipes,2001,1998,"Kevo Subarctic Research Institute, Finland",lab,male,male,NA,NA,60,60,60,60,0,0,596,596,animal_model,genetic_line,no,broad,authors,non_adult,non_adult,development time (number of days from the beginnig of the experiment to the cessation of feeding),final larval mass,reverse_maturation,size,include,cor,0.65,NA,NA,NA,NA,NA,NA,NA,NA,high,figure 2,maturation,size,genotype,0.775298706,60,-1,-0.775298706,male,non_adult,Insecta,between
2211,Priophorus pallipes,397,rayyan-697473009,Seasonally varying diet quality and the quantitative genetics of development time and body size in birch feeding insects,2001,NA,Finland,lab,male,male,NA,NA,NA,NA,22,22,NA,NA,304,304,animal_model,half_sib,no,broad,authors,non_adult,non_adult,development time,final larval mass,reverse_maturation,size,include,cor,0.48,0.2,se,NA,NA,NA,NA,NA,NA,male_broad,table 2,maturation,size,family,0.522984278,22,-1,-0.522984278,male,non_adult,Insecta,between
2212,Priophorus pallipes,397,rayyan-697473009,Seasonally varying diet quality and the quantitative genetics of development time and body size in birch feeding insects,2001,NA,Finland,lab,female,female,NA,NA,NA,NA,38,38,19,19,735,735,animal_model,half_sib,no,narrow,authors,non_adult,non_adult,development time,final larval mass,reverse_maturation,size,include,cor,0.77,0.21,se,NA,NA,NA,NA,NA,NA,female_narrow,table 2,maturation,size,family,1.020327758,38,-1,-1.020327758,female,non_adult,Insecta,between
2213,Priophorus pallipes,397,rayyan-697473009,Seasonally varying diet quality and the quantitative genetics of development time and body size in birch feeding insects,2001,NA,Finland,lab,female,female,NA,NA,NA,NA,38,38,19,19,735,735,animal_model,half_sib,no,broad,authors,non_adult,non_adult,development time,final larval mass,reverse_maturation,size,include,cor,0.09,0.44,se,NA,NA,NA,NA,NA,NA,female_broad,table 2,maturation,size,family,0.090244188,38,-1,-0.090244188,female,non_adult,Insecta,between
2214,Prostephanus truncatus,264,rayyan-197247454,"A phenotypic and genetic comparison of egg to adult life-history traits between and within two strains of the larger grain borer, Prostephanus truncatus (Horn) (Coleoptera: Bostrichidae)",1996,NA,NA,lab,both,both,NA,NA,NA,NA,50,50,NA,NA,348,348,family_mean_correlation,full_sib,no,narrow,authors,adult,non_adult,body weight at emergence,development period,size,reverse_maturation,include,cor,0.171,0.759,se,NA,NA,NA,NA,NA,NA,additive_genetic_correlation,quantitative genetics ,size,maturation,family,0.172696604,50,-1,-0.172696604,both,cross,Insecta,between
2216,Pungitius pungitius,356,rayyan-697472779,Quantitative genetics of body size and timing of maturation in two nine-spined stickleback (pungitius pungitius) populations,2011,2008,"Baltic Sea, Helsinki, Finland",lab,both,both,NA,NA,NA,NA,56,56,28,28,600,600,animal_model,half_sib,no,narrow,authors,both,non_adult,body size,timing of maturation (days after hatching),size,reverse_maturation,include,cor,0.24,"[-0.457, 0.610]",95CI,NA,NA,NA,NA,NA,NA,Helsinki_80_DAH,Genetics of body size and timing of maturation,size,maturation,family,0.244774113,56,-1,-0.244774113,both,cross,Actinopteri,between
2217,Pungitius pungitius,356,rayyan-697472779,Quantitative genetics of body size and timing of maturation in two nine-spined stickleback (pungitius pungitius) populations,2011,2008,"Baltic Sea, Helsinki, Finland",lab,both,both,NA,NA,NA,NA,56,56,28,28,602,602,animal_model,half_sib,no,narrow,authors,both,non_adult,body size,timing of maturation (days after hatching),size,reverse_maturation,include,cor,0.013,"[-0.607, 0.719]",95CI,NA,NA,NA,NA,NA,NA,Helsinki_110_DAH,Genetics of body size and timing of maturation,size,maturation,family,0.013000732,56,-1,-0.013000732,both,cross,Actinopteri,between
2218,Pungitius pungitius,356,rayyan-697472779,Quantitative genetics of body size and timing of maturation in two nine-spined stickleback (pungitius pungitius) populations,2011,2008,"Baltic Sea, Helsinki, Finland",lab,both,both,NA,NA,NA,NA,56,56,28,28,577,577,animal_model,half_sib,no,narrow,authors,both,non_adult,body size,timing of maturation (days after hatching),size,reverse_maturation,include,cor,0.874,"[0.725, 0.954]",95CI,NA,NA,NA,NA,NA,NA,Helsinki_140_DAH,Genetics of body size and timing of maturation,size,maturation,family,1.349774278,56,-1,-1.349774278,both,cross,Actinopteri,between
2219,Rana clamitans,139,rayyan-697472213,Growth and predation risk in green frog tadpoles (Rana clamitans): A quantitative genetic analysis,2006,NA,"Norwich, Vermont",lab,both,both,56,56,NA,NA,7,7,32,32,513,513,animal_model,full_sib,no,narrow,authors,non_adult,non_adult,size tadpole,growth tadpole,size,growth,include,cov,0.922703771,NA,NA,0.3396,NA,NA,0.4131,NA,NA,rayyan-697472213,table 2,size,growth,family,1.606921259,56,1,1.606921259,both,non_adult,Amphibia,between
2220,Rana sylvatica,140,rayyan-697472231,The heritability of inducible defenses in tadpoles,2005,1997,"E.S. George Reserve, Michigan, US",lab,both,both,54,54,NA,NA,54,54,21,21,540,540,sire_mean_correlation,full/half_sib,no,broad,CC,non_adult,non_adult,development,tadpole mass,maturation,size,include,cor,0.965,NA,NA,NA,NA,NA,NA,NA,NA,with_predator,table 4,maturation,size,family,2.013949731,54,1,2.013949731,both,non_adult,Amphibia,between
2221,Rana sylvatica,140,rayyan-697472231,The heritability of inducible defenses in tadpoles,2005,1997,"E.S. George Reserve, Michigan, US",lab,both,both,54,54,NA,NA,54,54,21,21,540,540,sire_mean_correlation,full/half_sib,no,broad,CC,non_adult,non_adult,development,body width,maturation,size,include,cor,0.08,NA,NA,NA,NA,NA,NA,NA,NA,without_predator,table 4,maturation,size,family,0.080171325,54,1,0.080171325,both,non_adult,Amphibia,between
2222,Rana sylvatica,140,rayyan-697472231,The heritability of inducible defenses in tadpoles,2005,1997,"E.S. George Reserve, Michigan, US",lab,both,both,54,54,NA,NA,54,54,21,21,540,540,sire_mean_correlation,full/half_sib,no,broad,CC,non_adult,non_adult,development,body length,maturation,size,include,cor,-0.404,NA,NA,NA,NA,NA,NA,NA,NA,without_predator,table 4,maturation,size,family,-0.428419959,54,1,-0.428419959,both,non_adult,Amphibia,between
2223,Rana sylvatica,140,rayyan-697472231,The heritability of inducible defenses in tadpoles,2005,1997,"E.S. George Reserve, Michigan, US",lab,both,both,54,54,NA,NA,54,54,21,21,540,540,sire_mean_correlation,full/half_sib,no,broad,CC,non_adult,non_adult,development,muscle width,maturation,size,include,cor,0.124,NA,NA,NA,NA,NA,NA,NA,NA,with_predator,table 4,maturation,size,family,0.12464147,54,1,0.12464147,both,non_adult,Amphibia,between
2224,Rana sylvatica,140,rayyan-697472231,The heritability of inducible defenses in tadpoles,2005,1997,"E.S. George Reserve, Michigan, US",lab,both,both,54,54,NA,NA,54,54,21,21,540,540,sire_mean_correlation,full/half_sib,no,broad,CC,non_adult,non_adult,development,body depth ,maturation,size,include,cor,-0.547,NA,NA,NA,NA,NA,NA,NA,NA,without_predator,table 4,maturation,size,family,-0.614090363,54,1,-0.614090363,both,non_adult,Amphibia,between
2225,Rana sylvatica,140,rayyan-697472231,The heritability of inducible defenses in tadpoles,2005,1997,"E.S. George Reserve, Michigan, US",lab,both,both,54,54,NA,NA,54,54,21,21,540,540,sire_mean_correlation,full/half_sib,no,broad,CC,non_adult,non_adult,development,muscle width,maturation,size,include,cor,0.482,NA,NA,NA,NA,NA,NA,NA,NA,without_predator,table 4,maturation,size,family,0.525586282,54,1,0.525586282,both,non_adult,Amphibia,between
2226,Rana sylvatica,140,rayyan-697472231,The heritability of inducible defenses in tadpoles,2005,1997,"E.S. George Reserve, Michigan, US",lab,both,both,54,54,NA,NA,54,54,21,21,540,540,sire_mean_correlation,full/half_sib,no,broad,CC,non_adult,non_adult,development,tail length,maturation,size,include,cor,0.131,NA,NA,NA,NA,NA,NA,NA,NA,with_predator,table 4,maturation,size,family,0.131757175,54,1,0.131757175,both,non_adult,Amphibia,between
2227,Rana sylvatica,140,rayyan-697472231,The heritability of inducible defenses in tadpoles,2005,1997,"E.S. George Reserve, Michigan, US",lab,both,both,54,54,NA,NA,54,54,21,21,540,540,sire_mean_correlation,full/half_sib,no,broad,CC,non_adult,non_adult,development,tail length,maturation,size,include,cor,0.084,NA,NA,NA,NA,NA,NA,NA,NA,without_predator,table 4,maturation,size,family,0.084198409,54,1,0.084198409,both,non_adult,Amphibia,between
2228,Rana sylvatica,140,rayyan-697472231,The heritability of inducible defenses in tadpoles,2005,1997,"E.S. George Reserve, Michigan, US",lab,both,both,54,54,NA,NA,54,54,21,21,540,540,sire_mean_correlation,full/half_sib,no,broad,CC,non_adult,non_adult,development,tadpole mass,maturation,size,include,cor,0.962,NA,NA,NA,NA,NA,NA,NA,NA,without_predator,table 4,maturation,size,family,1.97206674,54,1,1.97206674,both,non_adult,Amphibia,between
2229,Rana sylvatica,140,rayyan-697472231,The heritability of inducible defenses in tadpoles,2005,1997,"E.S. George Reserve, Michigan, US",lab,both,both,54,54,NA,NA,54,54,21,21,540,540,sire_mean_correlation,full/half_sib,no,broad,CC,non_adult,non_adult,development,muscle depth ,maturation,size,include,cor,0.182,NA,NA,NA,NA,NA,NA,NA,NA,without_predator,table 4,maturation,size,family,0.184050431,54,1,0.184050431,both,non_adult,Amphibia,between
2230,Rana sylvatica,140,rayyan-697472231,The heritability of inducible defenses in tadpoles,2005,1997,"E.S. George Reserve, Michigan, US",lab,both,both,54,54,NA,NA,54,54,21,21,540,540,sire_mean_correlation,full/half_sib,no,broad,CC,non_adult,non_adult,development,body depth ,maturation,size,include,cor,-0.309,NA,NA,NA,NA,NA,NA,NA,NA,with_predator,table 4,maturation,size,family,-0.319439471,54,1,-0.319439471,both,non_adult,Amphibia,between
2231,Rana sylvatica,140,rayyan-697472231,The heritability of inducible defenses in tadpoles,2005,1997,"E.S. George Reserve, Michigan, US",lab,both,both,54,54,NA,NA,54,54,21,21,540,540,sire_mean_correlation,full/half_sib,no,broad,CC,non_adult,non_adult,development,tail depth ,maturation,size,include,cor,0.808,NA,NA,NA,NA,NA,NA,NA,NA,with_predator,table 4,maturation,size,family,1.121240584,54,1,1.121240584,both,non_adult,Amphibia,between
2232,Rana sylvatica,140,rayyan-697472231,The heritability of inducible defenses in tadpoles,2005,1997,"E.S. George Reserve, Michigan, US",lab,both,both,54,54,NA,NA,54,54,21,21,540,540,sire_mean_correlation,full/half_sib,no,broad,CC,non_adult,non_adult,development,body width,maturation,size,include,cor,-0.452,NA,NA,NA,NA,NA,NA,NA,NA,with_predator,table 4,maturation,size,family,-0.487210954,54,1,-0.487210954,both,non_adult,Amphibia,between
2233,Rana sylvatica,140,rayyan-697472231,The heritability of inducible defenses in tadpoles,2005,1997,"E.S. George Reserve, Michigan, US",lab,both,both,54,54,NA,NA,54,54,21,21,540,540,sire_mean_correlation,full/half_sib,no,broad,CC,non_adult,non_adult,development,tail depth ,maturation,size,include,cor,0.401,NA,NA,NA,NA,NA,NA,NA,NA,without_predator,table 4,maturation,size,family,0.424839974,54,1,0.424839974,both,non_adult,Amphibia,between
2234,Rana sylvatica,140,rayyan-697472231,The heritability of inducible defenses in tadpoles,2005,1997,"E.S. George Reserve, Michigan, US",lab,both,both,54,54,NA,NA,54,54,21,21,540,540,sire_mean_correlation,full/half_sib,no,broad,CC,non_adult,non_adult,development,body length,maturation,size,include,cor,-0.652,NA,NA,NA,NA,NA,NA,NA,NA,with_predator,table 4,maturation,size,family,-0.778769737,54,1,-0.778769737,both,non_adult,Amphibia,between
2235,Rana sylvatica,140,rayyan-697472231,The heritability of inducible defenses in tadpoles,2005,1997,"E.S. George Reserve, Michigan, US",lab,both,both,54,54,NA,NA,54,54,21,21,540,540,sire_mean_correlation,full/half_sib,no,broad,CC,non_adult,non_adult,development,muscle depth ,maturation,size,include,cor,0.498,NA,NA,NA,NA,NA,NA,NA,NA,with_predator,table 4,maturation,size,family,0.546643022,54,1,0.546643022,both,non_adult,Amphibia,between
2236,Rana temporaria,61,rayyan-697471517,Evolution of the G-matrix in life history traits in the common frog during a recent colonisation of an island system,2012,2005,Gulf of Bothnia,lab,both,both,10,10,NA,NA,NA,NA,NA,NA,20,20,animal_model,full_sib,no,broad,authors,adult,non_adult,size at metamorphosis,developmental time to metamorphosis,size,reverse_maturation,include,cov,0.030096463,"[-0.70, 0.70]",95CI,0.69,"[0.21, 2.65]",95CI,0.64,"[0.2, 2.10]",95CI,Grissl_IT,table 1,size,maturation,family,0.030105555,10,-1,-0.030105555,both,cross,Amphibia,between
2237,Rana temporaria,61,rayyan-697471517,Evolution of the G-matrix in life history traits in the common frog during a recent colonisation of an island system,2012,2005,Gulf of Bothnia,lab,both,both,10,10,NA,NA,NA,NA,NA,NA,20,20,animal_model,full_sib,no,broad,authors,adult,non_adult,size at metamorphosis,developmental time to metamorphosis,size,reverse_maturation,include,cov,0.186771842,"[-0.63, 0.72]",95CI,0.54,"[0.18, 1.7]",95CI,0.43,"[0.15, 1.58]",95CI,Valvkal_MP,table 1,size,maturation,family,0.188990227,10,-1,-0.188990227,both,cross,Amphibia,between
2238,Rana temporaria,61,rayyan-697471517,Evolution of the G-matrix in life history traits in the common frog during a recent colonisation of an island system,2012,2005,Gulf of Bothnia,lab,both,both,10,10,NA,NA,NA,NA,NA,NA,20,20,animal_model,full_sib,no,broad,authors,adult,non_adult,size at metamorphosis,developmental time to metamorphosis,size,reverse_maturation,include,cov,0.166206896,"[-0.82, 0.92]",95CI,1.21,"[0.26, 9.65]",95CI,1.08,"[0.25, 10.11]",95CI,Fjardg_II,table 1,size,maturation,family,0.167763248,10,-1,-0.167763248,both,cross,Amphibia,between
2239,Rana temporaria,61,rayyan-697471517,Evolution of the G-matrix in life history traits in the common frog during a recent colonisation of an island system,2012,2005,Gulf of Bothnia,lab,both,both,10,10,NA,NA,NA,NA,NA,NA,20,20,animal_model,full_sib,no,broad,authors,adult,non_adult,size at metamorphosis,developmental time to metamorphosis,size,reverse_maturation,include,cov,0.633300496,"[-0.49, 0.80]",95CI,0.44,"[0.16, 1.44]",95CI,0.51,"[0.19, 1.76]",95CI,NedreM3_MP,table 1,size,maturation,family,0.746907685,10,-1,-0.746907685,both,cross,Amphibia,between
2240,Rana temporaria,61,rayyan-697471517,Evolution of the G-matrix in life history traits in the common frog during a recent colonisation of an island system,2012,2005,Gulf of Bothnia,lab,both,both,10,10,NA,NA,NA,NA,NA,NA,20,20,animal_model,full_sib,no,broad,authors,adult,non_adult,size at metamorphosis,developmental time to metamorphosis,size,reverse_maturation,include,cov,0.114122798,"[-0.69, 0.76]",95CI,0.63,"[0.17, 2.39]",95CI,0.78,"[0.28, 2.84]",95CI,Petlan_II,table 1,size,maturation,family,0.114622152,10,-1,-0.114622152,both,cross,Amphibia,between
2241,Rana temporaria,61,rayyan-697471517,Evolution of the G-matrix in life history traits in the common frog during a recent colonisation of an island system,2012,2005,Gulf of Bothnia,lab,both,both,10,10,NA,NA,NA,NA,NA,NA,20,20,animal_model,full_sib,no,broad,authors,adult,non_adult,size at metamorphosis,developmental time to metamorphosis,size,reverse_maturation,include,cov,0.348100566,"[-0.69, 0.91]",95CI,0.9,"[0.22, 4.24]",95CI,1.06,"[0.27, 6.38]",95CI,Svart_L_II,table 1,size,maturation,family,0.363280793,10,-1,-0.363280793,both,cross,Amphibia,between
2242,Rana temporaria,61,rayyan-697471517,Evolution of the G-matrix in life history traits in the common frog during a recent colonisation of an island system,2012,2005,Gulf of Bothnia,lab,both,both,10,10,NA,NA,NA,NA,NA,NA,20,20,animal_model,full_sib,no,broad,authors,adult,non_adult,size at metamorphosis,developmental time to metamorphosis,size,reverse_maturation,include,cov,0.374465431,"[-0.64, 0.89]",95CI,0.91,"[0.21, 5.55]",95CI,0.96,"[0.23, 5.31]",95CI,Vitskar_II,table 1,size,maturation,family,0.393606781,10,-1,-0.393606781,both,cross,Amphibia,between
2243,Rana temporaria,61,rayyan-697471517,Evolution of the G-matrix in life history traits in the common frog during a recent colonisation of an island system,2012,2005,Gulf of Bothnia,lab,both,both,10,10,NA,NA,NA,NA,NA,NA,20,20,animal_model,full_sib,no,broad,authors,adult,non_adult,size at metamorphosis,developmental time to metamorphosis,size,reverse_maturation,include,cov,0.591997322,"[-0.36, 0.81]",95CI,0.62,"[0.23, 1.86]",95CI,0.7,"[0.26, 2.05]",95CI,Lillkly_II,table 1,size,maturation,family,0.680735473,10,-1,-0.680735473,both,cross,Amphibia,between
2244,Rana temporaria,61,rayyan-697471517,Evolution of the G-matrix in life history traits in the common frog during a recent colonisation of an island system,2012,2005,Gulf of Bothnia,lab,both,both,10,10,NA,NA,NA,NA,NA,NA,20,20,animal_model,full_sib,no,broad,authors,adult,non_adult,size at metamorphosis,developmental time to metamorphosis,size,reverse_maturation,include,cov,0.6341673,"[-0.53, 0.85]",95CI,0.62,"[0.19, 2.62]",95CI,0.61,"[0.2, 2.39]",95CI,Buten_IP,table 1,size,maturation,family,0.748356267,10,-1,-0.748356267,both,cross,Amphibia,between
2245,Rana temporaria,61,rayyan-697471517,Evolution of the G-matrix in life history traits in the common frog during a recent colonisation of an island system,2012,2005,Gulf of Bothnia,lab,both,both,10,10,NA,NA,NA,NA,NA,NA,20,20,animal_model,full_sib,no,broad,authors,adult,non_adult,size at metamorphosis,developmental time to metamorphosis,size,reverse_maturation,include,cov,0.703562364,"[-0.48, 0.83]",95CI,0.44,"[0.15, 1.85]",95CI,0.5,"[0.17, 1.93]",95CI,Lillha_IP,table 1,size,maturation,family,0.874319992,10,-1,-0.874319992,both,cross,Amphibia,between
2250,Rana temporaria,61,rayyan-697471517,Evolution of the G-matrix in life history traits in the common frog during a recent colonisation of an island system,2012,2005,Gulf of Bothnia,lab,both,both,10,10,NA,NA,NA,NA,NA,NA,20,20,animal_model,full_sib,no,broad,authors,adult,non_adult,size at metamorphosis,developmental time to metamorphosis,size,reverse_maturation,include,cov,0.911371961,"[-0.27, 0.85]",95CI,0.53,"[0.18, 1.61]",95CI,0.46,"[0.16, 1.69]",95CI,NedreM2_MP,table 1,size,maturation,family,1.535564147,10,-1,-1.535564147,both,cross,Amphibia,between
2251,Rana temporaria,61,rayyan-697471517,Evolution of the G-matrix in life history traits in the common frog during a recent colonisation of an island system,2012,2005,Gulf of Bothnia,lab,both,both,10,10,NA,NA,NA,NA,NA,NA,20,20,animal_model,full_sib,no,broad,authors,adult,non_adult,size at metamorphosis,developmental time to metamorphosis,size,reverse_maturation,include,cov,0.115921741,"[0.58, 0.70]",95CI,0.47,"[0.17, 1.56]",95CI,0.57,"[0.18, 1.88]",95CI,Storha_IP,table 1,size,maturation,family,0.116445214,10,-1,-0.116445214,both,cross,Amphibia,between
2252,Rana temporaria,61,rayyan-697471517,Evolution of the G-matrix in life history traits in the common frog during a recent colonisation of an island system,2012,2005,Gulf of Bothnia,lab,both,both,10,10,NA,NA,NA,NA,NA,NA,20,20,animal_model,full_sib,no,broad,authors,adult,non_adult,size at metamorphosis,developmental time to metamorphosis,size,reverse_maturation,include,cov,0.319024409,"[-0.58, 0.82]",95CI,0.81,"[0.25, 3.37]",95CI,0.82,"[0.26, 3.37]",95CI,Gashall_II,table 1,size,maturation,family,0.330560597,10,-1,-0.330560597,both,cross,Amphibia,between
2255,Rana temporaria,61,rayyan-697471517,Evolution of the G-matrix in life history traits in the common frog during a recent colonisation of an island system,2012,2005,Gulf of Bothnia,lab,both,both,10,10,NA,NA,NA,NA,NA,NA,20,20,animal_model,full_sib,no,broad,authors,adult,non_adult,size at metamorphosis,developmental time to metamorphosis,size,reverse_maturation,include,cov,0.639660303,"[-0.37, 0.87]",95CI,0.65,"[0.20, 2.32]",95CI,0.94,"[0.33, 3.09]",95CI,Ahallan_IT,table 1,size,maturation,family,0.757598588,10,-1,-0.757598588,both,cross,Amphibia,between
2256,Rana temporaria,61,rayyan-697471517,Evolution of the G-matrix in life history traits in the common frog during a recent colonisation of an island system,2012,2005,Gulf of Bothnia,lab,both,both,10,10,NA,NA,NA,NA,NA,NA,20,20,animal_model,full_sib,no,broad,authors,adult,non_adult,size at metamorphosis,developmental time to metamorphosis,size,reverse_maturation,include,cov,0.723675961,"[-0.24, 0.87]",95CI,0.58,"[0.19, 1.86]",95CI,0.96,"[0.37, 2.58]",95CI,Bredska_IP,table 1,size,maturation,family,0.915320122,10,-1,-0.915320122,both,cross,Amphibia,between
2257,Rana temporaria,111,rayyan-697471814,Adaptive phenotypic plasticity and genetics of larval life histories in two Rana temporaria populations,2002,NA,"Esrange, Sweden",lab,both,both,45,45,NA,NA,45,45,45,45,810,810,animal_model,full_sib,no,narrow,authors,non_adult,adult,age at metamorphosis,mass at metamorphosis,reverse_maturation,size,include,cor,-0.383,0.087,se,NA,NA,NA,NA,NA,NA,noth_control_slow_fast_combined,table 4,maturation,size,family,-0.403570654,45,-1,0.403570654,both,cross,Amphibia,between
2258,Rana temporaria,61,rayyan-697471517,Evolution of the G-matrix in life history traits in the common frog during a recent colonisation of an island system,2012,2005,Gulf of Bothnia,lab,both,both,10,10,NA,NA,NA,NA,NA,NA,20,20,animal_model,full_sib,no,broad,authors,adult,non_adult,size at metamorphosis,developmental time to metamorphosis,size,reverse_maturation,include,cov,0.491353815,"[-0.53, 0.80]",95CI,0.56,"[0.18, 1.88]",95CI,0.5,"[0.16, 1.6]",95CI,Alvnarp_MP,table 1,size,maturation,family,0.537843465,10,-1,-0.537843465,both,cross,Amphibia,between
2259,Rana temporaria,61,rayyan-697471517,Evolution of the G-matrix in life history traits in the common frog during a recent colonisation of an island system,2012,2005,Gulf of Bothnia,lab,both,both,10,10,NA,NA,NA,NA,NA,NA,20,20,animal_model,full_sib,no,broad,authors,adult,non_adult,size at metamorphosis,developmental time to metamorphosis,size,reverse_maturation,include,cov,0.75055535,"[-0.25, 0.85]",95CI,0.64,"[0.22, 2.05]",95CI,0.75,"[0.26, 2.11]",95CI,Algrund_IT,table 1,size,maturation,family,0.974225656,10,-1,-0.974225656,both,cross,Amphibia,between
2260,Rana temporaria,61,rayyan-697471517,Evolution of the G-matrix in life history traits in the common frog during a recent colonisation of an island system,2012,2005,Gulf of Bothnia,lab,both,both,10,10,NA,NA,NA,NA,NA,NA,20,20,animal_model,full_sib,no,broad,authors,adult,non_adult,size at metamorphosis,developmental time to metamorphosis,size,reverse_maturation,include,cov,0.753762851,"[-0.37, 0.85]",95CI,0.54,"[0.17, 0.26]",95CI,0.72,"[0.25, 2.41]",95CI,Savar-T_IT,table 1,size,maturation,family,0.981611935,10,-1,-0.981611935,both,cross,Amphibia,between
2261,Rana temporaria,111,rayyan-697471814,Adaptive phenotypic plasticity and genetics of larval life histories in two Rana temporaria populations,2002,NA,"Tvedöra, Sweden",lab,both,both,45,45,NA,NA,45,45,45,45,810,810,animal_model,full_sib,no,narrow,authors,non_adult,adult,age at metamorphosis,mass at metamorphosis,reverse_maturation,size,include,cor,-0.43,0.121,se,NA,NA,NA,NA,NA,NA,south_control_slow_fast_combined,table 4,maturation,size,family,-0.459896681,45,-1,0.459896681,both,cross,Amphibia,between
2264,Rhopalosiphum padi,209,rayyan-197247274,Short-term population differences in the genetic architecture of life history traits related to sexuality in an aphid species,2008,NA,"Brittany, France",lab,female,female,NA,NA,43,43,NA,NA,NA,NA,129,129,animal_model,genetic_line,no,broad,authors,both,adult,longevity (number of days elapsed from birth to death),number of gynoparae (parthenogenetic females that produce sexual females only),survival,fertility,include,cor,-0.27,0.39,se,NA,NA,NA,NA,NA,NA,sexual_15,table 2,survival,fertility,genotype,-0.276863823,43,1,-0.276863823,female,cross,Insecta,between
2267,Rhopalosiphum padi,380,rayyan-697472902,Evolution of trade-offs between sexual and asexual phases and the role of reproductive plasticity in the genetic architecture of aphid life histories,2009,2002,"Brittany, France",lab,female,female,NA,NA,23,23,NA,NA,NA,NA,184,184,animal_model,genetic_line,no,broad,authors,adult,non_adult,number of apterous parthenogenetic females,Age at maturity,fertility,reverse_maturation,include,cor,0.07,0.28,se,NA,NA,NA,NA,NA,NA,Sexual,table 3,fertility,maturation,genotype,0.070114671,23,-1,-0.070114671,female,cross,Insecta,between
2268,Rhopalosiphum padi,209,rayyan-197247274,Short-term population differences in the genetic architecture of life history traits related to sexuality in an aphid species,2008,NA,"Brittany, France",lab,female,female,NA,NA,43,43,NA,NA,NA,NA,129,129,animal_model,genetic_line,no,broad,authors,non_adult,adult,mortality (number of dead offspring during the life of the focal individual),number of males,reverse_survival,fertility,include,cor,-0.48,0.48,se,NA,NA,NA,NA,NA,NA,sexual_15,table 2,survival,fertility,genotype,-0.522984278,43,-1,0.522984278,female,cross,Insecta,between
2269,Rhopalosiphum padi,380,rayyan-697472902,Evolution of trade-offs between sexual and asexual phases and the role of reproductive plasticity in the genetic architecture of aphid life histories,2009,2002,"Brittany, France",lab,female,female,NA,NA,23,23,NA,NA,NA,NA,184,184,animal_model,genetic_line,no,broad,authors,adult,adult,number of apterous parthenogenetic females,number of winged parthenogenetic females,fertility,fertility,include,cor,0.31,0.22,se,NA,NA,NA,NA,NA,NA,Sexual,table 3,fertility,fertility,genotype,0.320545409,23,1,0.320545409,female,adult,Insecta,within
2270,Rhopalosiphum padi,209,rayyan-197247274,Short-term population differences in the genetic architecture of life history traits related to sexuality in an aphid species,2008,NA,"Brittany, France",lab,female,female,NA,NA,43,43,NA,NA,NA,NA,129,129,animal_model,genetic_line,no,broad,authors,non_adult,adult,mortality (number of dead offspring during the life of the focal individual),total number of individuals,reverse_survival,fertility,include,cor,0.27,0.49,se,NA,NA,NA,NA,NA,NA,sexual_15,table 2,survival,fertility,genotype,0.276863823,43,-1,-0.276863823,female,cross,Insecta,between
2273,Rhopalosiphum padi,209,rayyan-197247274,Short-term population differences in the genetic architecture of life history traits related to sexuality in an aphid species,2008,NA,"Brittany, France",lab,female,female,NA,NA,53,53,NA,NA,NA,NA,159,159,animal_model,genetic_line,no,broad,authors,non_adult,both,age of first reproduction,longevity (number of days elapsed from birth to death),reverse_maturation,survival,include,cor,0.66,0.6,se,NA,NA,NA,NA,NA,NA,asexual_15,table 2,maturation,survival,genotype,0.792813632,53,-1,-0.792813632,female,cross,Insecta,between
2274,Rhopalosiphum padi,209,rayyan-197247274,Short-term population differences in the genetic architecture of life history traits related to sexuality in an aphid species,2008,NA,"Brittany, France",lab,female,female,NA,NA,53,53,NA,NA,NA,NA,159,159,animal_model,genetic_line,no,broad,authors,non_adult,both,age of first reproduction,longevity (number of days elapsed from birth to death),reverse_maturation,survival,include,cor,0.08,0.02,se,NA,NA,NA,NA,NA,NA,asexual_10,table 2,maturation,survival,genotype,0.080171325,53,-1,-0.080171325,female,cross,Insecta,between
2276,Rhopalosiphum padi,380,rayyan-697472902,Evolution of trade-offs between sexual and asexual phases and the role of reproductive plasticity in the genetic architecture of aphid life histories,2009,2002,"Brittany, France",lab,female,female,NA,NA,23,23,NA,NA,NA,NA,184,184,animal_model,genetic_line,no,broad,authors,adult,non_adult,Total fecundity,offspring mortality (total number of dead offspring during the life of the focal individual),fertility,reverse_survival,include,cor,0.18,0.32,se,NA,NA,NA,NA,NA,NA,Sexual,table 3,fertility,survival,genotype,0.181982689,23,-1,-0.181982689,female,cross,Insecta,between
2277,Rhopalosiphum padi,209,rayyan-197247274,Short-term population differences in the genetic architecture of life history traits related to sexuality in an aphid species,2008,NA,"Brittany, France",lab,female,female,NA,NA,53,53,NA,NA,NA,NA,159,159,animal_model,genetic_line,no,broad,authors,adult,adult,number of males,number of parthenogenetic females,fertility,fertility,include,cor,-0.4,0.28,se,NA,NA,NA,NA,NA,NA,asexual_10,table 2,fertility,fertility,genotype,-0.42364893,53,1,-0.42364893,female,adult,Insecta,within
2278,Rhopalosiphum padi,380,rayyan-697472902,Evolution of trade-offs between sexual and asexual phases and the role of reproductive plasticity in the genetic architecture of aphid life histories,2009,2002,"Brittany, France",lab,female,female,NA,NA,23,23,NA,NA,NA,NA,184,184,animal_model,genetic_line,no,broad,authors,adult,non_adult,number of apterous parthenogenetic females,offspring mortality (total number of dead offspring during the life of the focal individual),fertility,reverse_survival,include,cor,0.02,0.31,se,NA,NA,NA,NA,NA,NA,Sexual,table 3,fertility,survival,genotype,0.020002667,23,-1,-0.020002667,female,cross,Insecta,between
2280,Rhopalosiphum padi,209,rayyan-197247274,Short-term population differences in the genetic architecture of life history traits related to sexuality in an aphid species,2008,NA,"Brittany, France",lab,female,female,NA,NA,53,53,NA,NA,NA,NA,159,159,animal_model,genetic_line,no,broad,authors,adult,adult,number of parthenogenetic females,total number of individuals,fertility,fertility,include,cor,0.73,0.14,se,NA,NA,NA,NA,NA,NA,asexual_10,table 2,fertility,fertility,genotype,0.928727364,53,1,0.928727364,female,adult,Insecta,within
2282,Rhopalosiphum padi,209,rayyan-197247274,Short-term population differences in the genetic architecture of life history traits related to sexuality in an aphid species,2008,NA,"Brittany, France",lab,female,female,NA,NA,43,43,NA,NA,NA,NA,129,129,animal_model,genetic_line,no,broad,authors,adult,adult,number of males,number of parthenogenetic females,fertility,fertility,include,cor,0.33,0.24,se,NA,NA,NA,NA,NA,NA,sexual_15,table 2,fertility,fertility,genotype,0.342828254,43,1,0.342828254,female,adult,Insecta,within
2283,Rhopalosiphum padi,209,rayyan-197247274,Short-term population differences in the genetic architecture of life history traits related to sexuality in an aphid species,2008,NA,"Brittany, France",lab,female,female,NA,NA,43,43,NA,NA,NA,NA,129,129,animal_model,genetic_line,no,broad,authors,non_adult,adult,mortality (number of dead offspring during the life of the focal individual),number of parthenogenetic females,reverse_survival,fertility,include,cor,0.41,0.45,se,NA,NA,NA,NA,NA,NA,sexual_15,table 2,survival,fertility,genotype,0.435611223,43,-1,-0.435611223,female,cross,Insecta,between
2286,Rhopalosiphum padi,380,rayyan-697472902,Evolution of trade-offs between sexual and asexual phases and the role of reproductive plasticity in the genetic architecture of aphid life histories,2009,2002,"Brittany, France",lab,female,female,NA,NA,23,23,NA,NA,NA,NA,184,184,animal_model,genetic_line,no,broad,authors,adult,adult,Total fecundity,number of apterous parthenogenetic females,fertility,fertility,include,cor,0.83,0.092,se,NA,NA,NA,NA,NA,NA,Sexual,table 3,fertility,fertility,genotype,1.188136404,23,1,1.188136404,female,adult,Insecta,within
2287,Rhopalosiphum padi,380,rayyan-697472902,Evolution of trade-offs between sexual and asexual phases and the role of reproductive plasticity in the genetic architecture of aphid life histories,2009,2002,"Brittany, France",lab,female,female,NA,NA,23,23,NA,NA,NA,NA,184,184,animal_model,genetic_line,no,broad,authors,adult,adult,Total fecundity,number of winged parthenogenetic females,fertility,fertility,include,cor,0.47,0.19,se,NA,NA,NA,NA,NA,NA,Sexual,table 3,fertility,fertility,genotype,0.510070337,23,1,0.510070337,female,adult,Insecta,within
2288,Rhopalosiphum padi,209,rayyan-197247274,Short-term population differences in the genetic architecture of life history traits related to sexuality in an aphid species,2008,NA,"Brittany, France",lab,female,female,NA,NA,53,53,NA,NA,NA,NA,159,159,animal_model,genetic_line,no,broad,authors,non_adult,adult,age of first reproduction,number of males,reverse_maturation,fertility,include,cor,0.2,0.16,se,NA,NA,NA,NA,NA,NA,asexual_15,table 2,maturation,fertility,genotype,0.202732554,53,-1,-0.202732554,female,cross,Insecta,between
2289,Rhopalosiphum padi,209,rayyan-197247274,Short-term population differences in the genetic architecture of life history traits related to sexuality in an aphid species,2008,NA,"Brittany, France",lab,female,female,NA,NA,53,53,NA,NA,NA,NA,159,159,animal_model,genetic_line,no,broad,authors,non_adult,non_adult,age of first reproduction,mortality (number of dead offspring during the life of the focal individual),reverse_maturation,reverse_survival,include,cor,0.02,0.22,se,NA,NA,NA,NA,NA,NA,asexual_10,table 2,maturation,survival,genotype,0.020002667,53,1,0.020002667,female,non_adult,Insecta,between
2290,Rhopalosiphum padi,209,rayyan-197247274,Short-term population differences in the genetic architecture of life history traits related to sexuality in an aphid species,2008,NA,"Brittany, France",lab,female,female,NA,NA,53,53,NA,NA,NA,NA,159,159,animal_model,genetic_line,no,broad,authors,non_adult,adult,age of first reproduction,number of males,reverse_maturation,fertility,include,cor,-0.12,0.21,se,NA,NA,NA,NA,NA,NA,asexual_10,table 2,maturation,fertility,genotype,-0.120581028,53,-1,0.120581028,female,cross,Insecta,between
2291,Rhopalosiphum padi,209,rayyan-197247274,Short-term population differences in the genetic architecture of life history traits related to sexuality in an aphid species,2008,NA,"Brittany, France",lab,female,female,NA,NA,53,53,NA,NA,NA,NA,159,159,animal_model,genetic_line,no,broad,authors,non_adult,adult,age of first reproduction,number of parthenogenetic females,reverse_maturation,fertility,include,cor,-0.32,0.23,se,NA,NA,NA,NA,NA,NA,asexual_10,table 2,maturation,fertility,genotype,-0.331647109,53,-1,0.331647109,female,cross,Insecta,between
2293,Rhopalosiphum padi,209,rayyan-197247274,Short-term population differences in the genetic architecture of life history traits related to sexuality in an aphid species,2008,NA,"Brittany, France",lab,female,female,NA,NA,53,53,NA,NA,NA,NA,159,159,animal_model,genetic_line,no,broad,authors,both,adult,longevity (number of days elapsed from birth to death),number of males,survival,fertility,include,cor,0.52,0.63,se,NA,NA,NA,NA,NA,NA,asexual_10,table 2,survival,fertility,genotype,0.576339755,53,1,0.576339755,female,cross,Insecta,between
2294,Rhopalosiphum padi,209,rayyan-197247274,Short-term population differences in the genetic architecture of life history traits related to sexuality in an aphid species,2008,NA,"Brittany, France",lab,female,female,NA,NA,43,43,NA,NA,NA,NA,129,129,animal_model,genetic_line,no,broad,authors,non_adult,adult,mortality (number of dead offspring during the life of the focal individual),number of gynoparae (parthenogenetic females that produce sexual females only),reverse_survival,fertility,include,cor,0.19,0.45,se,NA,NA,NA,NA,NA,NA,sexual_15,table 2,survival,fertility,genotype,0.192337169,43,-1,-0.192337169,female,cross,Insecta,between
2295,Rhopalosiphum padi,209,rayyan-197247274,Short-term population differences in the genetic architecture of life history traits related to sexuality in an aphid species,2008,NA,"Brittany, France",lab,female,female,NA,NA,53,53,NA,NA,NA,NA,159,159,animal_model,genetic_line,no,broad,authors,both,adult,longevity (number of days elapsed from birth to death),number of parthenogenetic females,survival,fertility,include,cor,-0.06,0.96,se,NA,NA,NA,NA,NA,NA,asexual_10,table 2,survival,fertility,genotype,-0.060072156,53,1,-0.060072156,female,cross,Insecta,between
2296,Rhopalosiphum padi,380,rayyan-697472902,Evolution of trade-offs between sexual and asexual phases and the role of reproductive plasticity in the genetic architecture of aphid life histories,2009,2002,"Brittany, France",lab,female,female,NA,NA,23,23,NA,NA,NA,NA,184,184,animal_model,genetic_line,no,broad,authors,adult,non_adult,number of winged parthenogenetic females,Age at maturity,fertility,reverse_maturation,include,cor,0.12,0.28,se,NA,NA,NA,NA,NA,NA,Sexual,table 3,fertility,maturation,genotype,0.120581028,23,-1,-0.120581028,female,cross,Insecta,between
2297,Rhopalosiphum padi,209,rayyan-197247274,Short-term population differences in the genetic architecture of life history traits related to sexuality in an aphid species,2008,NA,"Brittany, France",lab,female,female,NA,NA,43,43,NA,NA,NA,NA,129,129,animal_model,genetic_line,no,broad,authors,adult,adult,total number of individuals,number of gynoparae (parthenogenetic females that produce sexual females only),fertility,fertility,include,cor,0.51,0.2,se,NA,NA,NA,NA,NA,NA,sexual_15,table 2,fertility,fertility,genotype,0.562729769,43,1,0.562729769,female,adult,Insecta,within
2298,Rhopalosiphum padi,380,rayyan-697472902,Evolution of trade-offs between sexual and asexual phases and the role of reproductive plasticity in the genetic architecture of aphid life histories,2009,2002,"Brittany, France",lab,female,female,NA,NA,23,23,NA,NA,NA,NA,184,184,animal_model,genetic_line,no,broad,authors,adult,non_adult,Total fecundity,Age at maturity,fertility,reverse_maturation,include,cor,0.25,0.27,se,NA,NA,NA,NA,NA,NA,Sexual,table 3,fertility,maturation,genotype,0.255412812,23,-1,-0.255412812,female,cross,Insecta,between
2299,Rhopalosiphum padi,209,rayyan-197247274,Short-term population differences in the genetic architecture of life history traits related to sexuality in an aphid species,2008,NA,"Brittany, France",lab,female,female,NA,NA,53,53,NA,NA,NA,NA,159,159,animal_model,genetic_line,no,broad,authors,non_adult,adult,mortality (number of dead offspring during the life of the focal individual),total number of individuals,reverse_survival,fertility,include,cor,0.13,0.32,se,NA,NA,NA,NA,NA,NA,asexual_10,table 2,survival,fertility,genotype,0.13073985,53,-1,-0.13073985,female,cross,Insecta,between
2301,Rhopalosiphum padi,380,rayyan-697472902,Evolution of trade-offs between sexual and asexual phases and the role of reproductive plasticity in the genetic architecture of aphid life histories,2009,2002,"Brittany, France",lab,female,female,NA,NA,23,23,NA,NA,NA,NA,184,184,animal_model,genetic_line,no,broad,authors,adult,adult,number of apterous parthenogenetic females,number of gynoparae,fertility,fertility,include,cor,-0.81,0.083,se,NA,NA,NA,NA,NA,NA,Sexual,table 3,fertility,fertility,genotype,-1.127029026,23,1,-1.127029026,female,adult,Insecta,within
2303,Rhopalosiphum padi,380,rayyan-697472902,Evolution of trade-offs between sexual and asexual phases and the role of reproductive plasticity in the genetic architecture of aphid life histories,2009,2002,"Brittany, France",lab,female,female,NA,NA,23,23,NA,NA,NA,NA,184,184,animal_model,genetic_line,no,broad,authors,non_adult,non_adult,Age at maturity,offspring mortality (total number of dead offspring during the life of the focal individual),reverse_maturation,reverse_survival,include,cor,-0.06,0.38,se,NA,NA,NA,NA,NA,NA,asexual,table 3,maturation,survival,genotype,-0.060072156,23,1,-0.060072156,female,non_adult,Insecta,between
2304,Rhopalosiphum padi,209,rayyan-197247274,Short-term population differences in the genetic architecture of life history traits related to sexuality in an aphid species,2008,NA,"Brittany, France",lab,female,female,NA,NA,43,43,NA,NA,NA,NA,129,129,animal_model,genetic_line,no,broad,authors,both,adult,longevity (number of days elapsed from birth to death),total number of individuals,survival,fertility,include,cor,0.47,0.33,se,NA,NA,NA,NA,NA,NA,sexual_15,table 2,survival,fertility,genotype,0.510070337,43,1,0.510070337,female,cross,Insecta,between
2307,Rhopalosiphum padi,209,rayyan-197247274,Short-term population differences in the genetic architecture of life history traits related to sexuality in an aphid species,2008,NA,"Brittany, France",lab,female,female,NA,NA,53,53,NA,NA,NA,NA,159,159,animal_model,genetic_line,no,broad,authors,non_adult,non_adult,age of first reproduction,mortality (number of dead offspring during the life of the focal individual),reverse_maturation,reverse_survival,include,cor,-0.12,0.21,se,NA,NA,NA,NA,NA,NA,asexual_15,table 2,maturation,survival,genotype,-0.120581028,53,1,-0.120581028,female,non_adult,Insecta,between
2309,Rhopalosiphum padi,209,rayyan-197247274,Short-term population differences in the genetic architecture of life history traits related to sexuality in an aphid species,2008,NA,"Brittany, France",lab,female,female,NA,NA,53,53,NA,NA,NA,NA,159,159,animal_model,genetic_line,no,broad,authors,both,adult,longevity (number of days elapsed from birth to death),total number of individuals,survival,fertility,include,cor,0.4,0.64,se,NA,NA,NA,NA,NA,NA,asexual_10,table 2,survival,fertility,genotype,0.42364893,53,1,0.42364893,female,cross,Insecta,between
2310,Rhopalosiphum padi,209,rayyan-197247274,Short-term population differences in the genetic architecture of life history traits related to sexuality in an aphid species,2008,NA,"Brittany, France",lab,female,female,NA,NA,43,43,NA,NA,NA,NA,129,129,animal_model,genetic_line,no,broad,authors,adult,adult,number of parthenogenetic females,number of gynoparae (parthenogenetic females that produce sexual females only),fertility,fertility,include,cor,-0.21,0.22,se,NA,NA,NA,NA,NA,NA,sexual_15,table 2,fertility,fertility,genotype,-0.213171347,43,1,-0.213171347,female,adult,Insecta,within
2311,Rhopalosiphum padi,209,rayyan-197247274,Short-term population differences in the genetic architecture of life history traits related to sexuality in an aphid species,2008,NA,"Brittany, France",lab,female,female,NA,NA,43,43,NA,NA,NA,NA,129,129,animal_model,genetic_line,no,broad,authors,adult,adult,number of parthenogenetic females,total number of individuals,fertility,fertility,include,cor,0.33,0.24,se,NA,NA,NA,NA,NA,NA,sexual_15,table 2,fertility,fertility,genotype,0.342828254,43,1,0.342828254,female,adult,Insecta,within
2315,Rhopalosiphum padi,209,rayyan-197247274,Short-term population differences in the genetic architecture of life history traits related to sexuality in an aphid species,2008,NA,"Brittany, France",lab,female,female,NA,NA,53,53,NA,NA,NA,NA,159,159,animal_model,genetic_line,no,broad,authors,non_adult,adult,mortality (number of dead offspring during the life of the focal individual),number of males,reverse_survival,fertility,include,cor,0.73,0.12,se,NA,NA,NA,NA,NA,NA,asexual_15,table 2,survival,fertility,genotype,0.928727364,53,-1,-0.928727364,female,cross,Insecta,between
2316,Rhopalosiphum padi,209,rayyan-197247274,Short-term population differences in the genetic architecture of life history traits related to sexuality in an aphid species,2008,NA,"Brittany, France",lab,female,female,NA,NA,53,53,NA,NA,NA,NA,159,159,animal_model,genetic_line,no,broad,authors,non_adult,adult,mortality (number of dead offspring during the life of the focal individual),number of parthenogenetic females,reverse_survival,fertility,include,cor,-0.78,0.11,se,NA,NA,NA,NA,NA,NA,asexual_15,table 2,survival,fertility,genotype,-1.045370548,53,-1,1.045370548,female,cross,Insecta,between
2317,Rhopalosiphum padi,209,rayyan-197247274,Short-term population differences in the genetic architecture of life history traits related to sexuality in an aphid species,2008,NA,"Brittany, France",lab,female,female,NA,NA,53,53,NA,NA,NA,NA,159,159,animal_model,genetic_line,no,broad,authors,non_adult,adult,mortality (number of dead offspring during the life of the focal individual),total number of individuals,reverse_survival,fertility,include,cor,-0.06,0.31,se,NA,NA,NA,NA,NA,NA,asexual_15,table 2,survival,fertility,genotype,-0.060072156,53,-1,0.060072156,female,cross,Insecta,between
2318,Rhopalosiphum padi,351,rayyan-697472756,The effects of reproductive specialization on energy costs and fitness genetic variances in cyclical and obligate parthenogenetic aphids,2012,2006-2008,"Brittany, France",lab,female,female,NA,NA,35,35,NA,NA,NA,NA,280,280,animal_model,genetic_line,no,broad,authors,adult,adult,Adult body mass,Lifetime reproduction,size,fertility,include,cor,NA,0.31,se,NA,NA,NA,NA,NA,NA,Asexual_sexual_combined,table 3,size,fertility,genotype,NA,35,1,NA,female,adult,Insecta,between
2319,Rhopalosiphum padi,209,rayyan-197247274,Short-term population differences in the genetic architecture of life history traits related to sexuality in an aphid species,2008,NA,"Brittany, France",lab,female,female,NA,NA,53,53,NA,NA,NA,NA,159,159,animal_model,genetic_line,no,broad,authors,non_adult,adult,age of first reproduction,total number of individuals,reverse_maturation,fertility,include,cor,-0.41,0.25,se,NA,NA,NA,NA,NA,NA,asexual_10,table 2,maturation,fertility,genotype,-0.435611223,53,-1,0.435611223,female,cross,Insecta,between
2321,Rhopalosiphum padi,351,rayyan-697472756,The effects of reproductive specialization on energy costs and fitness genetic variances in cyclical and obligate parthenogenetic aphids,2012,2006-2008,"Brittany, France",lab,female,female,NA,NA,35,35,NA,NA,NA,NA,280,280,animal_model,genetic_line,no,broad,authors,non_adult,adult,Age at maturity,Lifetime reproduction,reverse_maturation,fertility,include,cor,-0.88,0.36,se,NA,NA,NA,NA,NA,NA,Asexual_sexual_combined,table 3,maturation,fertility,genotype,-1.375767657,35,-1,1.375767657,female,cross,Insecta,between
2322,Rhopalosiphum padi,380,rayyan-697472902,Evolution of trade-offs between sexual and asexual phases and the role of reproductive plasticity in the genetic architecture of aphid life histories,2009,2002,"Brittany, France",lab,female,female,NA,NA,23,23,NA,NA,NA,NA,184,184,animal_model,genetic_line,no,broad,authors,adult,adult,Total fecundity,Apterous parthenogenetic females,fertility,fertility,include,cor,0.72,0.18,se,NA,NA,NA,NA,NA,NA,asexual,table 3,fertility,fertility,genotype,0.907644983,23,1,0.907644983,female,adult,Insecta,within
2323,Rhopalosiphum padi,209,rayyan-197247274,Short-term population differences in the genetic architecture of life history traits related to sexuality in an aphid species,2008,NA,"Brittany, France",lab,female,female,NA,NA,53,53,NA,NA,NA,NA,159,159,animal_model,genetic_line,no,broad,authors,non_adult,adult,mortality (number of dead offspring during the life of the focal individual),number of males,reverse_survival,fertility,include,cor,0.61,0.21,se,NA,NA,NA,NA,NA,NA,asexual_10,table 2,survival,fertility,genotype,0.708921359,53,-1,-0.708921359,female,cross,Insecta,between
2324,Rhopalosiphum padi,209,rayyan-197247274,Short-term population differences in the genetic architecture of life history traits related to sexuality in an aphid species,2008,NA,"Brittany, France",lab,female,female,NA,NA,53,53,NA,NA,NA,NA,159,159,animal_model,genetic_line,no,broad,authors,non_adult,adult,mortality (number of dead offspring during the life of the focal individual),number of parthenogenetic females,reverse_survival,fertility,include,cor,-0.53,0.24,se,NA,NA,NA,NA,NA,NA,asexual_10,table 2,survival,fertility,genotype,-0.59014516,53,-1,0.59014516,female,cross,Insecta,between
2328,Rhopalosiphum padi,351,rayyan-697472756,The effects of reproductive specialization on energy costs and fitness genetic variances in cyclical and obligate parthenogenetic aphids,2012,2006-2008,"Brittany, France",lab,female,female,NA,NA,35,35,NA,NA,NA,NA,280,280,animal_model,genetic_line,no,broad,authors,adult,non_adult,Adult body mass,Age at maturity,size,reverse_maturation,include,cor,-0.42,0.32,se,NA,NA,NA,NA,NA,NA,Asexual_sexual_combined,table 3,size,maturation,genotype,-0.447692024,35,-1,0.447692024,female,cross,Insecta,between
2329,Rhopalosiphum padi,351,rayyan-697472756,The effects of reproductive specialization on energy costs and fitness genetic variances in cyclical and obligate parthenogenetic aphids,2012,2006-2008,"Brittany, France",lab,female,female,NA,NA,35,35,NA,NA,NA,NA,280,280,animal_model,genetic_line,no,broad,authors,adult,adult,Adult body mass,Apterous females,size,fertility,include,cor,0.98,0.21,se,NA,NA,NA,NA,NA,NA,Asexual_sexual_combined,table 3,size,fertility,genotype,2.297559925,35,1,2.297559925,female,adult,Insecta,between
2330,Rhopalosiphum padi,351,rayyan-697472756,The effects of reproductive specialization on energy costs and fitness genetic variances in cyclical and obligate parthenogenetic aphids,2012,2006-2008,"Brittany, France",lab,female,female,NA,NA,35,35,NA,NA,NA,NA,280,280,animal_model,genetic_line,no,broad,authors,adult,adult,Adult body mass,Winged females,size,fertility,include,cor,0.66,0.59,se,NA,NA,NA,NA,NA,NA,Asexual_sexual_combined,table 3,size,fertility,genotype,0.792813632,35,1,0.792813632,female,adult,Insecta,between
2331,Rhopalosiphum padi,209,rayyan-197247274,Short-term population differences in the genetic architecture of life history traits related to sexuality in an aphid species,2008,NA,"Brittany, France",lab,female,female,NA,NA,43,43,NA,NA,NA,NA,129,129,animal_model,genetic_line,no,broad,authors,both,adult,longevity (number of days elapsed from birth to death),number of parthenogenetic females,survival,fertility,include,cor,0.02,0.36,se,NA,NA,NA,NA,NA,NA,sexual_15,table 2,survival,fertility,genotype,0.020002667,43,1,0.020002667,female,cross,Insecta,between
2332,Rhopalosiphum padi,209,rayyan-197247274,Short-term population differences in the genetic architecture of life history traits related to sexuality in an aphid species,2008,NA,"Brittany, France",lab,female,female,NA,NA,53,53,NA,NA,NA,NA,159,159,animal_model,genetic_line,no,broad,authors,adult,adult,number of males,number of parthenogenetic females,fertility,fertility,include,cor,-0.82,0.07,se,NA,NA,NA,NA,NA,NA,asexual_15,table 2,fertility,fertility,genotype,-1.156817465,53,1,-1.156817465,female,adult,Insecta,within
2333,Rhopalosiphum padi,209,rayyan-197247274,Short-term population differences in the genetic architecture of life history traits related to sexuality in an aphid species,2008,NA,"Brittany, France",lab,female,female,NA,NA,53,53,NA,NA,NA,NA,159,159,animal_model,genetic_line,no,broad,authors,both,non_adult,longevity (number of days elapsed from birth to death),mortality (number of dead offspring during the life of the focal individual),survival,reverse_survival,include,cor,0.34,0.08,se,NA,NA,NA,NA,NA,NA,asexual_10,table 2,survival,survival,genotype,0.354092529,53,-1,-0.354092529,female,cross,Insecta,within
2334,Rhopalosiphum padi,209,rayyan-197247274,Short-term population differences in the genetic architecture of life history traits related to sexuality in an aphid species,2008,NA,"Brittany, France",lab,female,female,NA,NA,53,53,NA,NA,NA,NA,159,159,animal_model,genetic_line,no,broad,authors,adult,adult,number of parthenogenetic females,total number of individuals,fertility,fertility,include,cor,0.96,0.02,se,NA,NA,NA,NA,NA,NA,asexual_15,table 2,fertility,fertility,genotype,1.945910149,53,1,1.945910149,female,adult,Insecta,within
2335,Rhopalosiphum padi,209,rayyan-197247274,Short-term population differences in the genetic architecture of life history traits related to sexuality in an aphid species,2008,NA,"Brittany, France",lab,female,female,NA,NA,43,43,NA,NA,NA,NA,129,129,animal_model,genetic_line,no,broad,authors,non_adult,both,age of first reproduction,longevity (number of days elapsed from birth to death),reverse_maturation,survival,include,cor,-0.68,1.3,se,NA,NA,NA,NA,NA,NA,sexual_10,table 2,maturation,survival,genotype,-0.829114038,43,-1,0.829114038,female,cross,Insecta,between
2336,Rhopalosiphum padi,209,rayyan-197247274,Short-term population differences in the genetic architecture of life history traits related to sexuality in an aphid species,2008,NA,"Brittany, France",lab,female,female,NA,NA,43,43,NA,NA,NA,NA,129,129,animal_model,genetic_line,no,broad,authors,adult,adult,number of males,total number of individuals,fertility,fertility,include,cor,0.31,0.27,se,NA,NA,NA,NA,NA,NA,sexual_15,table 2,fertility,fertility,genotype,0.320545409,43,1,0.320545409,female,adult,Insecta,within
2337,Rhopalosiphum padi,209,rayyan-197247274,Short-term population differences in the genetic architecture of life history traits related to sexuality in an aphid species,2008,NA,"Brittany, France",lab,female,female,NA,NA,43,43,NA,NA,NA,NA,129,129,animal_model,genetic_line,no,broad,authors,adult,adult,number of males,number of gynoparae (parthenogenetic females that produce sexual females only),fertility,fertility,include,cor,-0.27,0.27,se,NA,NA,NA,NA,NA,NA,sexual_15,table 2,fertility,fertility,genotype,-0.276863823,43,1,-0.276863823,female,adult,Insecta,within
2338,Rhopalosiphum padi,351,rayyan-697472756,The effects of reproductive specialization on energy costs and fitness genetic variances in cyclical and obligate parthenogenetic aphids,2012,2006-2008,"Brittany, France",lab,female,female,NA,NA,35,35,NA,NA,NA,NA,280,280,animal_model,genetic_line,no,broad,authors,adult,adult,Apterous females,Lifetime reproduction,fertility,fertility,include,cor,0.01,1.56,se,NA,NA,NA,NA,NA,NA,Asexual_sexual_combined,table 3,fertility,fertility,genotype,0.010000333,35,1,0.010000333,female,adult,Insecta,within
2340,Rhopalosiphum padi,351,rayyan-697472756,The effects of reproductive specialization on energy costs and fitness genetic variances in cyclical and obligate parthenogenetic aphids,2012,2006-2008,"Brittany, France",lab,female,female,NA,NA,35,35,NA,NA,NA,NA,280,280,animal_model,genetic_line,no,broad,authors,adult,adult,Winged females,Lifetime reproduction,fertility,fertility,include,cor,0.001,0.6,se,NA,NA,NA,NA,NA,NA,Asexual_sexual_combined,table 3,fertility,fertility,genotype,0.001,35,1,0.001,female,adult,Insecta,within
2343,Rhopalosiphum padi,209,rayyan-197247274,Short-term population differences in the genetic architecture of life history traits related to sexuality in an aphid species,2008,NA,"Brittany, France",lab,female,female,NA,NA,53,53,NA,NA,NA,NA,159,159,animal_model,genetic_line,no,broad,authors,adult,adult,number of males,total number of individuals,fertility,fertility,include,cor,0.27,0.3,se,NA,NA,NA,NA,NA,NA,asexual_10,table 2,fertility,fertility,genotype,0.276863823,53,1,0.276863823,female,adult,Insecta,within
2344,Rhopalosiphum padi,380,rayyan-697472902,Evolution of trade-offs between sexual and asexual phases and the role of reproductive plasticity in the genetic architecture of aphid life histories,2009,2002,"Brittany, France",lab,female,female,NA,NA,23,23,NA,NA,NA,NA,184,184,animal_model,genetic_line,no,broad,authors,adult,adult,number of apterous parthenogenetic females,number of males,fertility,fertility,include,cor,-0.75,0.11,se,NA,NA,NA,NA,NA,NA,Sexual,table 3,fertility,fertility,genotype,-0.972955075,23,1,-0.972955075,female,adult,Insecta,within
2345,Rhopalosiphum padi,380,rayyan-697472902,Evolution of trade-offs between sexual and asexual phases and the role of reproductive plasticity in the genetic architecture of aphid life histories,2009,2002,"Brittany, France",lab,female,female,NA,NA,23,23,NA,NA,NA,NA,184,184,animal_model,genetic_line,no,broad,authors,adult,adult,number of winged parthenogenetic females,number of gynoparae,fertility,fertility,include,cor,-0.48,0.19,se,NA,NA,NA,NA,NA,NA,Sexual,table 3,fertility,fertility,genotype,-0.522984278,23,1,-0.522984278,female,adult,Insecta,within
2346,Rhopalosiphum padi,209,rayyan-197247274,Short-term population differences in the genetic architecture of life history traits related to sexuality in an aphid species,2008,NA,"Brittany, France",lab,female,female,NA,NA,53,53,NA,NA,NA,NA,159,159,animal_model,genetic_line,no,broad,authors,adult,adult,number of males,total number of individuals,fertility,fertility,include,cor,0.25,0.25,se,NA,NA,NA,NA,NA,NA,asexual_15,table 2,fertility,fertility,genotype,0.255412812,53,1,0.255412812,female,adult,Insecta,within
2347,Rhopalosiphum padi,351,rayyan-697472756,The effects of reproductive specialization on energy costs and fitness genetic variances in cyclical and obligate parthenogenetic aphids,2012,2006-2008,"Brittany, France",lab,female,female,NA,NA,35,35,NA,NA,NA,NA,280,280,animal_model,genetic_line,no,broad,authors,non_adult,adult,Age at maturity,Apterous females,reverse_maturation,fertility,include,cor,-0.6,0.39,se,NA,NA,NA,NA,NA,NA,Asexual_sexual_combined,table 3,maturation,fertility,genotype,-0.693147181,35,-1,0.693147181,female,cross,Insecta,between
2348,Rhopalosiphum padi,351,rayyan-697472756,The effects of reproductive specialization on energy costs and fitness genetic variances in cyclical and obligate parthenogenetic aphids,2012,2006-2008,"Brittany, France",lab,female,female,NA,NA,35,35,NA,NA,NA,NA,280,280,animal_model,genetic_line,no,broad,authors,non_adult,adult,Age at maturity,Winged females,reverse_maturation,fertility,include,cor,-0.97,0.53,se,NA,NA,NA,NA,NA,NA,Asexual_sexual_combined,table 3,maturation,fertility,genotype,-2.09229572,35,-1,2.09229572,female,cross,Insecta,between
2350,Rhopalosiphum padi,351,rayyan-697472756,The effects of reproductive specialization on energy costs and fitness genetic variances in cyclical and obligate parthenogenetic aphids,2012,2006-2008,"Brittany, France",lab,female,female,NA,NA,35,35,NA,NA,NA,NA,280,280,animal_model,genetic_line,no,broad,authors,adult,adult,Apterous females,Winged females,fertility,fertility,include,cor,0.01,0.62,se,NA,NA,NA,NA,NA,NA,Asexual_sexual_combined,table 3,fertility,fertility,genotype,0.010000333,35,1,0.010000333,female,adult,Insecta,within
2352,Rhopalosiphum padi,209,rayyan-197247274,Short-term population differences in the genetic architecture of life history traits related to sexuality in an aphid species,2008,NA,"Brittany, France",lab,female,female,NA,NA,53,53,NA,NA,NA,NA,159,159,animal_model,genetic_line,no,broad,authors,both,adult,longevity (number of days elapsed from birth to death),number of males,survival,fertility,include,cor,0.4,0.56,se,NA,NA,NA,NA,NA,NA,asexual_15,table 2,survival,fertility,genotype,0.42364893,53,1,0.42364893,female,cross,Insecta,between
2353,Rhopalosiphum padi,209,rayyan-197247274,Short-term population differences in the genetic architecture of life history traits related to sexuality in an aphid species,2008,NA,"Brittany, France",lab,female,female,NA,NA,53,53,NA,NA,NA,NA,159,159,animal_model,genetic_line,no,broad,authors,both,adult,longevity (number of days elapsed from birth to death),number of parthenogenetic females,survival,fertility,include,cor,-0.1,0.5,se,NA,NA,NA,NA,NA,NA,asexual_15,table 2,survival,fertility,genotype,-0.100335348,53,1,-0.100335348,female,cross,Insecta,between
2354,Rhopalosiphum padi,209,rayyan-197247274,Short-term population differences in the genetic architecture of life history traits related to sexuality in an aphid species,2008,NA,"Brittany, France",lab,female,female,NA,NA,53,53,NA,NA,NA,NA,159,159,animal_model,genetic_line,no,broad,authors,both,adult,longevity (number of days elapsed from birth to death),total number of individuals,survival,fertility,include,cor,-0.1,0.55,se,NA,NA,NA,NA,NA,NA,asexual_15,table 2,survival,fertility,genotype,-0.100335348,53,1,-0.100335348,female,cross,Insecta,between
2355,Rhopalosiphum padi,380,rayyan-697472902,Evolution of trade-offs between sexual and asexual phases and the role of reproductive plasticity in the genetic architecture of aphid life histories,2009,2002,"Brittany, France",lab,female,female,NA,NA,23,23,NA,NA,NA,NA,184,184,animal_model,genetic_line,no,broad,authors,adult,adult,Total fecundity,number of males,fertility,fertility,include,cor,-0.47,0.2,se,NA,NA,NA,NA,NA,NA,Sexual,table 3,fertility,fertility,genotype,-0.510070337,23,1,-0.510070337,female,adult,Insecta,within
2356,Rhopalosiphum padi,209,rayyan-197247274,Short-term population differences in the genetic architecture of life history traits related to sexuality in an aphid species,2008,NA,"Brittany, France",lab,female,female,NA,NA,43,43,NA,NA,NA,NA,129,129,animal_model,genetic_line,no,broad,authors,both,adult,longevity (number of days elapsed from birth to death),number of gynoparae (parthenogenetic females that produce sexual females only),survival,fertility,include,cor,0.18,0.4,se,NA,NA,NA,NA,NA,NA,sexual_10,table 2,survival,fertility,genotype,0.181982689,43,1,0.181982689,female,cross,Insecta,between
2357,Rhopalosiphum padi,380,rayyan-697472902,Evolution of trade-offs between sexual and asexual phases and the role of reproductive plasticity in the genetic architecture of aphid life histories,2009,2002,"Brittany, France",lab,female,female,NA,NA,23,23,NA,NA,NA,NA,184,184,animal_model,genetic_line,no,broad,authors,adult,non_adult,number of winged parthenogenetic females,offspring mortality (total number of dead offspring during the life of the focal individual),fertility,reverse_survival,include,cor,-0.09,0.36,se,NA,NA,NA,NA,NA,NA,asexual,table 3,fertility,survival,genotype,-0.090244188,23,-1,0.090244188,female,cross,Insecta,between
2358,Rhopalosiphum padi,209,rayyan-197247274,Short-term population differences in the genetic architecture of life history traits related to sexuality in an aphid species,2008,NA,"Brittany, France",lab,female,female,NA,NA,43,43,NA,NA,NA,NA,129,129,animal_model,genetic_line,no,broad,authors,non_adult,adult,mortality (number of dead offspring during the life of the focal individual),number of males,reverse_survival,fertility,include,cor,-0.21,0.28,se,NA,NA,NA,NA,NA,NA,sexual_10,table 2,survival,fertility,genotype,-0.213171347,43,-1,0.213171347,female,cross,Insecta,between
2360,Rhopalosiphum padi,209,rayyan-197247274,Short-term population differences in the genetic architecture of life history traits related to sexuality in an aphid species,2008,NA,"Brittany, France",lab,female,female,NA,NA,43,43,NA,NA,NA,NA,129,129,animal_model,genetic_line,no,broad,authors,non_adult,adult,mortality (number of dead offspring during the life of the focal individual),number of gynoparae (parthenogenetic females that produce sexual females only),reverse_survival,fertility,include,cor,0.06,0.23,se,NA,NA,NA,NA,NA,NA,sexual_10,table 2,survival,fertility,genotype,0.060072156,43,-1,-0.060072156,female,cross,Insecta,between
2361,Rhopalosiphum padi,380,rayyan-697472902,Evolution of trade-offs between sexual and asexual phases and the role of reproductive plasticity in the genetic architecture of aphid life histories,2009,2002,"Brittany, France",lab,female,female,NA,NA,23,23,NA,NA,NA,NA,184,184,animal_model,genetic_line,no,broad,authors,non_adult,adult,Age at maturity,number of gynoparae,reverse_maturation,fertility,include,cor,0.26,0.26,se,NA,NA,NA,NA,NA,NA,Sexual,table 3,maturation,fertility,genotype,0.266108407,23,-1,-0.266108407,female,cross,Insecta,between
2362,Rhopalosiphum padi,209,rayyan-197247274,Short-term population differences in the genetic architecture of life history traits related to sexuality in an aphid species,2008,NA,"Brittany, France",lab,female,female,NA,NA,43,43,NA,NA,NA,NA,129,129,animal_model,genetic_line,no,broad,authors,adult,adult,total number of individuals,number of gynoparae (parthenogenetic females that produce sexual females only),fertility,fertility,include,cor,0.91,0.06,se,NA,NA,NA,NA,NA,NA,sexual_10,table 2,fertility,fertility,genotype,1.527524425,43,1,1.527524425,female,adult,Insecta,within
2363,Rhopalosiphum padi,380,rayyan-697472902,Evolution of trade-offs between sexual and asexual phases and the role of reproductive plasticity in the genetic architecture of aphid life histories,2009,2002,"Brittany, France",lab,female,female,NA,NA,23,23,NA,NA,NA,NA,184,184,animal_model,genetic_line,no,broad,authors,adult,adult,Total fecundity,Winged parthenogenetic females,fertility,fertility,include,cor,-0.36,0.34,se,NA,NA,NA,NA,NA,NA,asexual,table 3,fertility,fertility,genotype,-0.376885901,23,1,-0.376885901,female,adult,Insecta,within
2365,Rhopalosiphum padi,380,rayyan-697472902,Evolution of trade-offs between sexual and asexual phases and the role of reproductive plasticity in the genetic architecture of aphid life histories,2009,2002,"Brittany, France",lab,female,female,NA,NA,23,23,NA,NA,NA,NA,184,184,animal_model,genetic_line,no,broad,authors,adult,non_adult,number of gynoparae,offspring mortality (total number of dead offspring during the life of the focal individual),fertility,reverse_survival,include,cor,-0.29,0.29,se,NA,NA,NA,NA,NA,NA,Sexual,table 3,fertility,survival,genotype,-0.298566264,23,-1,0.298566264,female,cross,Insecta,between
2366,Rhopalosiphum padi,380,rayyan-697472902,Evolution of trade-offs between sexual and asexual phases and the role of reproductive plasticity in the genetic architecture of aphid life histories,2009,2002,"Brittany, France",lab,female,female,NA,NA,23,23,NA,NA,NA,NA,184,184,animal_model,genetic_line,no,broad,authors,adult,non_adult,number of males,offspring mortality (total number of dead offspring during the life of the focal individual),fertility,reverse_survival,include,cor,-0.04,0.32,se,NA,NA,NA,NA,NA,NA,Sexual,table 3,fertility,survival,genotype,-0.040021354,23,-1,0.040021354,female,cross,Insecta,between
2368,Rhopalosiphum padi,380,rayyan-697472902,Evolution of trade-offs between sexual and asexual phases and the role of reproductive plasticity in the genetic architecture of aphid life histories,2009,2002,"Brittany, France",lab,female,female,NA,NA,23,23,NA,NA,NA,NA,184,184,animal_model,genetic_line,no,broad,authors,adult,non_adult,number of apterous parthenogenetic females,offspring mortality (total number of dead offspring during the life of the focal individual),fertility,reverse_survival,include,cor,-0.06,0.34,se,NA,NA,NA,NA,NA,NA,asexual,table 3,fertility,survival,genotype,-0.060072156,23,-1,0.060072156,female,cross,Insecta,between
2369,Rhopalosiphum padi,380,rayyan-697472902,Evolution of trade-offs between sexual and asexual phases and the role of reproductive plasticity in the genetic architecture of aphid life histories,2009,2002,"Brittany, France",lab,female,female,NA,NA,23,23,NA,NA,NA,NA,184,184,animal_model,genetic_line,no,broad,authors,adult,non_adult,number of winged parthenogenetic females,Age at maturity,fertility,reverse_maturation,include,cor,-0.24,0.32,se,NA,NA,NA,NA,NA,NA,asexual,table 3,fertility,maturation,genotype,-0.244774113,23,-1,0.244774113,female,cross,Insecta,between
2370,Rhopalosiphum padi,209,rayyan-197247274,Short-term population differences in the genetic architecture of life history traits related to sexuality in an aphid species,2008,NA,"Brittany, France",lab,female,female,NA,NA,43,43,NA,NA,NA,NA,129,129,animal_model,genetic_line,no,broad,authors,both,non_adult,longevity (number of days elapsed from birth to death),mortality (number of dead offspring during the life of the focal individual),survival,reverse_survival,include,cor,0.02,0.74,se,NA,NA,NA,NA,NA,NA,sexual_15,table 2,survival,survival,genotype,0.020002667,43,-1,-0.020002667,female,cross,Insecta,within
2371,Rhopalosiphum padi,209,rayyan-197247274,Short-term population differences in the genetic architecture of life history traits related to sexuality in an aphid species,2008,NA,"Brittany, France",lab,female,female,NA,NA,43,43,NA,NA,NA,NA,129,129,animal_model,genetic_line,no,broad,authors,both,adult,longevity (number of days elapsed from birth to death),number of males,survival,fertility,include,cor,0.78,0.26,se,NA,NA,NA,NA,NA,NA,sexual_15,table 2,survival,fertility,genotype,1.045370548,43,1,1.045370548,female,cross,Insecta,between
2372,Rhopalosiphum padi,209,rayyan-197247274,Short-term population differences in the genetic architecture of life history traits related to sexuality in an aphid species,2008,NA,"Brittany, France",lab,female,female,NA,NA,43,43,NA,NA,NA,NA,129,129,animal_model,genetic_line,no,broad,authors,non_adult,adult,mortality (number of dead offspring during the life of the focal individual),total number of individuals,reverse_survival,fertility,include,cor,0.07,0.26,se,NA,NA,NA,NA,NA,NA,sexual_10,table 2,survival,fertility,genotype,0.070114671,43,-1,-0.070114671,female,cross,Insecta,between
2373,Rhopalosiphum padi,380,rayyan-697472902,Evolution of trade-offs between sexual and asexual phases and the role of reproductive plasticity in the genetic architecture of aphid life histories,2009,2002,"Brittany, France",lab,female,female,NA,NA,23,23,NA,NA,NA,NA,184,184,animal_model,genetic_line,no,broad,authors,adult,non_adult,Total fecundity,Age at maturity,fertility,reverse_maturation,include,cor,-0.89,0.21,se,NA,NA,NA,NA,NA,NA,asexual,table 3,fertility,maturation,genotype,-1.421925871,23,-1,1.421925871,female,cross,Insecta,between
2374,Rhopalosiphum padi,380,rayyan-697472902,Evolution of trade-offs between sexual and asexual phases and the role of reproductive plasticity in the genetic architecture of aphid life histories,2009,2002,"Brittany, France",lab,female,female,NA,NA,23,23,NA,NA,NA,NA,184,184,animal_model,genetic_line,no,broad,authors,adult,non_adult,Total fecundity,offspring mortality (total number of dead offspring during the life of the focal individual),fertility,reverse_survival,include,cor,-0.08,0.4,se,NA,NA,NA,NA,NA,NA,asexual,table 3,fertility,survival,genotype,-0.080171325,23,-1,0.080171325,female,cross,Insecta,between
2375,Rhopalosiphum padi,380,rayyan-697472902,Evolution of trade-offs between sexual and asexual phases and the role of reproductive plasticity in the genetic architecture of aphid life histories,2009,2002,"Brittany, France",lab,female,female,NA,NA,23,23,NA,NA,NA,NA,184,184,animal_model,genetic_line,no,broad,authors,non_adult,adult,Age at maturity,number of males,reverse_maturation,fertility,include,cor,-0.11,0.28,se,NA,NA,NA,NA,NA,NA,asexual,table 3,maturation,fertility,genotype,-0.110446916,23,-1,0.110446916,female,cross,Insecta,between
2377,Rhopalosiphum padi,209,rayyan-197247274,Short-term population differences in the genetic architecture of life history traits related to sexuality in an aphid species,2008,NA,"Brittany, France",lab,female,female,NA,NA,43,43,NA,NA,NA,NA,129,129,animal_model,genetic_line,no,broad,authors,both,adult,longevity (number of days elapsed from birth to death),number of males,survival,fertility,include,cor,0.05,0.65,se,NA,NA,NA,NA,NA,NA,sexual_10,table 2,survival,fertility,genotype,0.050041729,43,1,0.050041729,female,cross,Insecta,between
2378,Rhopalosiphum padi,209,rayyan-197247274,Short-term population differences in the genetic architecture of life history traits related to sexuality in an aphid species,2008,NA,"Brittany, France",lab,female,female,NA,NA,43,43,NA,NA,NA,NA,129,129,animal_model,genetic_line,no,broad,authors,both,adult,longevity (number of days elapsed from birth to death),total number of individuals,survival,fertility,include,cor,0.17,0.41,se,NA,NA,NA,NA,NA,NA,sexual_10,table 2,survival,fertility,genotype,0.171666664,43,1,0.171666664,female,cross,Insecta,between
2381,Rhopalosiphum padi,209,rayyan-197247274,Short-term population differences in the genetic architecture of life history traits related to sexuality in an aphid species,2008,NA,"Brittany, France",lab,female,female,NA,NA,43,43,NA,NA,NA,NA,129,129,animal_model,genetic_line,no,broad,authors,adult,adult,number of males,total number of individuals,fertility,fertility,include,cor,-0.41,0.29,se,NA,NA,NA,NA,NA,NA,sexual_10,table 2,fertility,fertility,genotype,-0.435611223,43,1,-0.435611223,female,adult,Insecta,within
2383,Rhopalosiphum padi,380,rayyan-697472902,Evolution of trade-offs between sexual and asexual phases and the role of reproductive plasticity in the genetic architecture of aphid life histories,2009,2002,"Brittany, France",lab,female,female,NA,NA,23,23,NA,NA,NA,NA,184,184,animal_model,genetic_line,no,broad,authors,adult,adult,Total fecundity,number of gynoparae,fertility,fertility,include,cor,-0.6,0.16,se,NA,NA,NA,NA,NA,NA,Sexual,table 3,fertility,fertility,genotype,-0.693147181,23,1,-0.693147181,female,adult,Insecta,within
2384,Rhopalosiphum padi,380,rayyan-697472902,Evolution of trade-offs between sexual and asexual phases and the role of reproductive plasticity in the genetic architecture of aphid life histories,2009,2002,"Brittany, France",lab,female,female,NA,NA,23,23,NA,NA,NA,NA,184,184,animal_model,genetic_line,no,broad,authors,adult,adult,number of winged parthenogenetic females,number of males,fertility,fertility,include,cor,-0.56,0.17,se,NA,NA,NA,NA,NA,NA,Sexual,table 3,fertility,fertility,genotype,-0.632833187,23,1,-0.632833187,female,adult,Insecta,within
2385,Rhopalosiphum padi,209,rayyan-197247274,Short-term population differences in the genetic architecture of life history traits related to sexuality in an aphid species,2008,NA,"Brittany, France",lab,female,female,NA,NA,43,43,NA,NA,NA,NA,129,129,animal_model,genetic_line,no,broad,authors,both,non_adult,longevity (number of days elapsed from birth to death),mortality (number of dead offspring during the life of the focal individual),survival,reverse_survival,include,cor,-0.68,0.74,se,NA,NA,NA,NA,NA,NA,sexual_10,table 2,survival,survival,genotype,-0.829114038,43,-1,0.829114038,female,cross,Insecta,within
2386,Rhopalosiphum padi,209,rayyan-197247274,Short-term population differences in the genetic architecture of life history traits related to sexuality in an aphid species,2008,NA,"Brittany, France",lab,female,female,NA,NA,43,43,NA,NA,NA,NA,129,129,animal_model,genetic_line,no,broad,authors,non_adult,adult,age of first reproduction,total number of individuals,reverse_maturation,fertility,include,cor,-0.37,0.25,se,NA,NA,NA,NA,NA,NA,sexual_15,table 2,maturation,fertility,genotype,-0.3884231,43,-1,0.3884231,female,cross,Insecta,between
2387,Rhopalosiphum padi,209,rayyan-197247274,Short-term population differences in the genetic architecture of life history traits related to sexuality in an aphid species,2008,NA,"Brittany, France",lab,female,female,NA,NA,53,53,NA,NA,NA,NA,159,159,animal_model,genetic_line,no,broad,authors,non_adult,adult,age of first reproduction,total number of individuals,reverse_maturation,fertility,include,cor,-0.11,0.2,se,NA,NA,NA,NA,NA,NA,asexual_15,table 2,maturation,fertility,genotype,-0.110446916,53,-1,0.110446916,female,cross,Insecta,between
2388,Rhopalosiphum padi,209,rayyan-197247274,Short-term population differences in the genetic architecture of life history traits related to sexuality in an aphid species,2008,NA,"Brittany, France",lab,female,female,NA,NA,53,53,NA,NA,NA,NA,159,159,animal_model,genetic_line,no,broad,authors,both,non_adult,longevity (number of days elapsed from birth to death),mortality (number of dead offspring during the life of the focal individual),survival,reverse_survival,include,cor,-0.02,0.59,se,NA,NA,NA,NA,NA,NA,asexual_15,table 2,survival,survival,genotype,-0.020002667,53,-1,0.020002667,female,cross,Insecta,within
2389,Rhopalosiphum padi,209,rayyan-197247274,Short-term population differences in the genetic architecture of life history traits related to sexuality in an aphid species,2008,NA,"Brittany, France",lab,female,female,NA,NA,43,43,NA,NA,NA,NA,129,129,animal_model,genetic_line,no,broad,authors,non_adult,adult,age of first reproduction,number of gynoparae (parthenogenetic females that produce sexual females only),reverse_maturation,fertility,include,cor,0.68,0.57,se,NA,NA,NA,NA,NA,NA,sexual_10,table 2,maturation,fertility,genotype,0.829114038,43,-1,-0.829114038,female,cross,Insecta,between
2390,Rhopalosiphum padi,209,rayyan-197247274,Short-term population differences in the genetic architecture of life history traits related to sexuality in an aphid species,2008,NA,"Brittany, France",lab,female,female,NA,NA,43,43,NA,NA,NA,NA,129,129,animal_model,genetic_line,no,broad,authors,non_adult,adult,age of first reproduction,number of parthenogenetic females,reverse_maturation,fertility,include,cor,0.1,0.23,se,NA,NA,NA,NA,NA,NA,sexual_15,table 2,maturation,fertility,genotype,0.100335348,43,-1,-0.100335348,female,cross,Insecta,between
2391,Rhopalosiphum padi,209,rayyan-197247274,Short-term population differences in the genetic architecture of life history traits related to sexuality in an aphid species,2008,NA,"Brittany, France",lab,female,female,NA,NA,43,43,NA,NA,NA,NA,129,129,animal_model,genetic_line,no,broad,authors,non_adult,adult,age of first reproduction,number of gynoparae (parthenogenetic females that produce sexual females only),reverse_maturation,fertility,include,cor,-0.38,0.22,se,NA,NA,NA,NA,NA,NA,sexual_15,table 2,maturation,fertility,genotype,-0.40005965,43,-1,0.40005965,female,cross,Insecta,between
2392,Rhopalosiphum padi,380,rayyan-697472902,Evolution of trade-offs between sexual and asexual phases and the role of reproductive plasticity in the genetic architecture of aphid life histories,2009,2002,"Brittany, France",lab,female,female,NA,NA,23,23,NA,NA,NA,NA,184,184,animal_model,genetic_line,no,broad,authors,adult,non_adult,number of apterous parthenogenetic females,Age at maturity,fertility,reverse_maturation,include,cor,-0.22,0.3,se,NA,NA,NA,NA,NA,NA,asexual,table 3,fertility,maturation,genotype,-0.223656109,23,-1,0.223656109,female,cross,Insecta,between
2393,Rhopalosiphum padi,209,rayyan-197247274,Short-term population differences in the genetic architecture of life history traits related to sexuality in an aphid species,2008,NA,"Brittany, France",lab,female,female,NA,NA,43,43,NA,NA,NA,NA,129,129,animal_model,genetic_line,no,broad,authors,non_adult,non_adult,age of first reproduction,mortality (number of dead offspring during the life of the focal individual),reverse_maturation,reverse_survival,include,cor,0.46,0.5,se,NA,NA,NA,NA,NA,NA,sexual_15,table 2,maturation,survival,genotype,0.497311288,43,1,0.497311288,female,non_adult,Insecta,between
2394,Rhopalosiphum padi,209,rayyan-197247274,Short-term population differences in the genetic architecture of life history traits related to sexuality in an aphid species,2008,NA,"Brittany, France",lab,female,female,NA,NA,43,43,NA,NA,NA,NA,129,129,animal_model,genetic_line,no,broad,authors,non_adult,adult,age of first reproduction,number of males,reverse_maturation,fertility,include,cor,0.24,0.27,se,NA,NA,NA,NA,NA,NA,sexual_15,table 2,maturation,fertility,genotype,0.244774113,43,-1,-0.244774113,female,cross,Insecta,between
2395,Rhopalosiphum padi,209,rayyan-197247274,Short-term population differences in the genetic architecture of life history traits related to sexuality in an aphid species,2008,NA,"Brittany, France",lab,female,female,NA,NA,43,43,NA,NA,NA,NA,129,129,animal_model,genetic_line,no,broad,authors,non_adult,both,age of first reproduction,longevity (number of days elapsed from birth to death),reverse_maturation,survival,include,cor,-0.16,0.38,se,NA,NA,NA,NA,NA,NA,sexual_15,table 2,maturation,survival,genotype,-0.161386696,43,-1,0.161386696,female,cross,Insecta,between
2396,Rhopalosiphum padi,209,rayyan-197247274,Short-term population differences in the genetic architecture of life history traits related to sexuality in an aphid species,2008,NA,"Brittany, France",lab,female,female,NA,NA,43,43,NA,NA,NA,NA,129,129,animal_model,genetic_line,no,broad,authors,non_adult,adult,age of first reproduction,total number of individuals,reverse_maturation,fertility,include,cor,0.56,0.47,se,NA,NA,NA,NA,NA,NA,sexual_10,table 2,maturation,fertility,genotype,0.632833187,43,-1,-0.632833187,female,cross,Insecta,between
2397,Rhopalosiphum padi,209,rayyan-197247274,Short-term population differences in the genetic architecture of life history traits related to sexuality in an aphid species,2008,NA,"Brittany, France",lab,female,female,NA,NA,43,43,NA,NA,NA,NA,129,129,animal_model,genetic_line,no,broad,authors,non_adult,adult,age of first reproduction,number of males,reverse_maturation,fertility,include,cor,-0.32,0.37,se,NA,NA,NA,NA,NA,NA,sexual_10,table 2,maturation,fertility,genotype,-0.331647109,43,-1,0.331647109,female,cross,Insecta,between
2398,Rhopalosiphum padi,380,rayyan-697472902,Evolution of trade-offs between sexual and asexual phases and the role of reproductive plasticity in the genetic architecture of aphid life histories,2009,2002,"Brittany, France",lab,female,female,NA,NA,23,23,NA,NA,NA,NA,184,184,animal_model,genetic_line,no,broad,authors,adult,non_adult,number of winged parthenogenetic females,offspring mortality (total number of dead offspring during the life of the focal individual),fertility,reverse_survival,include,cor,0.51,0.26,se,NA,NA,NA,NA,NA,NA,Sexual,table 3,fertility,survival,genotype,0.562729769,23,-1,-0.562729769,female,cross,Insecta,between
2399,Rhopalosiphum padi,209,rayyan-197247274,Short-term population differences in the genetic architecture of life history traits related to sexuality in an aphid species,2008,NA,"Brittany, France",lab,female,female,NA,NA,53,53,NA,NA,NA,NA,159,159,animal_model,genetic_line,no,broad,authors,non_adult,adult,age of first reproduction,number of parthenogenetic females,reverse_maturation,fertility,include,cor,-0.12,0.18,se,NA,NA,NA,NA,NA,NA,asexual_15,table 2,maturation,fertility,genotype,-0.120581028,53,-1,0.120581028,female,cross,Insecta,between
2400,Rhopalosiphum padi,380,rayyan-697472902,Evolution of trade-offs between sexual and asexual phases and the role of reproductive plasticity in the genetic architecture of aphid life histories,2009,2002,"Brittany, France",lab,female,female,NA,NA,23,23,NA,NA,NA,NA,184,184,animal_model,genetic_line,no,broad,authors,adult,adult,number of apterous parthenogenetic females,Winged parthenogenetic females,fertility,fertility,include,cor,-0.9,0.07,se,NA,NA,NA,NA,NA,NA,asexual,table 3,fertility,fertility,genotype,-1.47221949,23,1,-1.47221949,female,adult,Insecta,within
2401,Rhopalosiphum padi,380,rayyan-697472902,Evolution of trade-offs between sexual and asexual phases and the role of reproductive plasticity in the genetic architecture of aphid life histories,2009,2002,"Brittany, France",lab,female,female,NA,NA,23,23,NA,NA,NA,NA,184,184,animal_model,genetic_line,no,broad,authors,non_adult,non_adult,Age at maturity,offspring mortality (total number of dead offspring during the life of the focal individual),reverse_maturation,reverse_survival,include,cor,0.02,0.37,se,NA,NA,NA,NA,NA,NA,Sexual,table 3,maturation,survival,genotype,0.020002667,23,1,0.020002667,female,non_adult,Insecta,between
2402,Rhopalosiphum padi,380,rayyan-697472902,Evolution of trade-offs between sexual and asexual phases and the role of reproductive plasticity in the genetic architecture of aphid life histories,2009,2002,"Brittany, France",lab,female,female,NA,NA,23,23,NA,NA,NA,NA,184,184,animal_model,genetic_line,no,broad,authors,adult,adult,number of gynoparae,number of males,fertility,fertility,include,cor,0.64,0.15,se,NA,NA,NA,NA,NA,NA,Sexual,table 3,fertility,fertility,genotype,0.758173745,23,1,0.758173745,female,adult,Insecta,within
2403,Rhopalosiphum padi,209,rayyan-197247274,Short-term population differences in the genetic architecture of life history traits related to sexuality in an aphid species,2008,NA,"Brittany, France",lab,female,female,NA,NA,43,43,NA,NA,NA,NA,129,129,animal_model,genetic_line,no,broad,authors,adult,adult,number of males,number of gynoparae (parthenogenetic females that produce sexual females only),fertility,fertility,include,cor,-0.73,0.15,se,NA,NA,NA,NA,NA,NA,sexual_10,table 2,fertility,fertility,genotype,-0.928727364,43,1,-0.928727364,female,adult,Insecta,within
2404,Rhopalosiphum padi,209,rayyan-197247274,Short-term population differences in the genetic architecture of life history traits related to sexuality in an aphid species,2008,NA,"Brittany, France",lab,female,female,NA,NA,43,43,NA,NA,NA,NA,129,129,animal_model,genetic_line,no,broad,authors,non_adult,non_adult,age of first reproduction,mortality (number of dead offspring during the life of the focal individual),reverse_maturation,reverse_survival,include,cor,0.99,0.24,se,NA,NA,NA,NA,NA,NA,sexual_10,table 2,maturation,survival,genotype,2.646652412,43,1,2.646652412,female,non_adult,Insecta,between
2407,Salamandra salamandra,296,rayyan-197247871,"Variability in survival, growth and metamorphosis in the larval fire salamander (Salamandra Salamandra): Effects of larval birth size, sibship and environment",2004,1994,"Puerto de Mijares, Spain",lab,both,both,NA,NA,NA,NA,5,5,NA,NA,55,55,animal_model,full_sib,no,broad,authors,non_adult,non_adult,larval size at birth,mass-specific growth from birth to metamorphosis,size,growth,include,cor,-0.93,NA,NA,NA,NA,NA,NA,NA,NA,rg_low_temp_high_food,table 2,size,growth,family,-1.65839002,5,1,-1.65839002,both,non_adult,Amphibia,between
2409,Salamandra salamandra,296,rayyan-197247871,"Variability in survival, growth and metamorphosis in the larval fire salamander (Salamandra Salamandra): Effects of larval birth size, sibship and environment",2004,1994,"Puerto de Mijares, Spain",lab,both,both,NA,NA,NA,NA,5,5,NA,NA,49,49,animal_model,full_sib,no,broad,authors,non_adult,adult,larval size at birth,size at metamorphosis,size,size,include,cor,0.14,NA,NA,NA,NA,NA,NA,NA,NA,rg_high_temp_high_food,table 2,size,size,family,0.140925576,5,1,0.140925576,both,cross,Amphibia,within
2410,Salamandra salamandra,296,rayyan-197247871,"Variability in survival, growth and metamorphosis in the larval fire salamander (Salamandra Salamandra): Effects of larval birth size, sibship and environment",2004,1994,"Puerto de Mijares, Spain",lab,both,both,NA,NA,NA,NA,5,5,NA,NA,53,53,animal_model,full_sib,no,broad,authors,non_adult,adult,larval size at birth,size at metamorphosis,size,size,include,cor,0.61,NA,NA,NA,NA,NA,NA,NA,NA,rg_low_temp_low_food,table 2,size,size,family,0.708921359,5,1,0.708921359,both,cross,Amphibia,within
2413,Salamandra salamandra,296,rayyan-197247871,"Variability in survival, growth and metamorphosis in the larval fire salamander (Salamandra Salamandra): Effects of larval birth size, sibship and environment",2004,1994,"Puerto de Mijares, Spain",lab,both,both,NA,NA,NA,NA,5,5,NA,NA,55,55,animal_model,full_sib,no,broad,authors,non_adult,adult,larval size at birth,size at metamorphosis,size,size,include,cor,0.4,NA,NA,NA,NA,NA,NA,NA,NA,rg_low_temp_high_food,table 2,size,size,family,0.42364893,5,1,0.42364893,both,cross,Amphibia,within
2416,Salamandra salamandra,296,rayyan-197247871,"Variability in survival, growth and metamorphosis in the larval fire salamander (Salamandra Salamandra): Effects of larval birth size, sibship and environment",2004,1994,"Puerto de Mijares, Spain",lab,both,both,NA,NA,NA,NA,5,5,NA,NA,49,49,animal_model,full_sib,no,broad,authors,non_adult,non_adult,larval size at birth,mass-specific growth from birth to metamorphosis,size,growth,include,cor,-0.18,NA,NA,NA,NA,NA,NA,NA,NA,rg_high_temp_high_food,table 2,size,growth,family,-0.181982689,5,1,-0.181982689,both,non_adult,Amphibia,between
2418,Salamandra salamandra,296,rayyan-197247871,"Variability in survival, growth and metamorphosis in the larval fire salamander (Salamandra Salamandra): Effects of larval birth size, sibship and environment",2004,1994,"Puerto de Mijares, Spain",lab,both,both,NA,NA,NA,NA,5,5,NA,NA,53,53,animal_model,full_sib,no,broad,authors,non_adult,non_adult,larval size at birth,mass-specific growth from birth to metamorphosis,size,growth,include,cor,-0.74,NA,NA,NA,NA,NA,NA,NA,NA,rg_low_temp_low_food,table 2,size,growth,family,-0.950479381,5,1,-0.950479381,both,non_adult,Amphibia,between
2423,Salmo salar,365,rayyan-697472821,Alternative life histories in the Atlantic salmon: Genetic covariances within the sneaker sexual tactic in males,2011,2004-2006,"Que´bec, Canada",lab,male,male,24,24,NA,NA,4,4,14,14,574,574,animal_model,half_sib,no,narrow,authors,both,non_adult,July body mass,Timing of early sexual maturity (number of days after hatched),size,reverse_maturation,include,cor,NA,0.143,se,NA,NA,NA,NA,NA,NA,rayyan-697472821,table s2,size,maturation,family,NA,24,-1,NA,male,cross,Actinopteri,between
2424,Salmo salar,365,rayyan-697472821,Alternative life histories in the Atlantic salmon: Genetic covariances within the sneaker sexual tactic in males,2011,2004-2006,"Que´bec, Canada",lab,male,male,24,24,NA,NA,4,4,14,14,574,574,animal_model,half_sib,no,narrow,authors,adult,non_adult,emergence length,Timing of early sexual maturity (number of days after hatched),size,reverse_maturation,include,cor,-0.286,0.515,se,NA,NA,NA,NA,NA,NA,rayyan-697472821,table s2,size,maturation,family,-0.294204471,24,-1,0.294204471,male,cross,Actinopteri,between
2425,Salmo salar,365,rayyan-697472821,Alternative life histories in the Atlantic salmon: Genetic covariances within the sneaker sexual tactic in males,2011,2004-2006,"Que´bec, Canada",lab,male,male,24,24,NA,NA,4,4,14,14,574,574,animal_model,half_sib,no,narrow,authors,both,non_adult,April length,Timing of early sexual maturity (number of days after hatched),size,reverse_maturation,include,cor,0.591,0.321,se,NA,NA,NA,NA,NA,NA,rayyan-697472821,table s2,size,maturation,family,0.679201436,24,-1,-0.679201436,male,cross,Actinopteri,between
2426,Salmo salar,365,rayyan-697472821,Alternative life histories in the Atlantic salmon: Genetic covariances within the sneaker sexual tactic in males,2011,2004-2006,"Que´bec, Canada",lab,male,male,24,24,NA,NA,4,4,14,14,574,574,animal_model,half_sib,no,narrow,authors,both,non_adult,April body depth,Timing of early sexual maturity (number of days after hatched),size,reverse_maturation,include,cor,0.61,0.304,se,NA,NA,NA,NA,NA,NA,rayyan-697472821,table s2,size,maturation,family,0.708921359,24,-1,-0.708921359,male,cross,Actinopteri,between
2427,Salmo salar,365,rayyan-697472821,Alternative life histories in the Atlantic salmon: Genetic covariances within the sneaker sexual tactic in males,2011,2004-2006,"Que´bec, Canada",lab,male,male,24,24,NA,NA,4,4,14,14,574,574,animal_model,half_sib,no,narrow,authors,both,non_adult,January body depth,Timing of early sexual maturity (number of days after hatched),size,reverse_maturation,include,cor,0.241,0.463,se,NA,NA,NA,NA,NA,NA,rayyan-697472821,table s2,size,maturation,family,0.245835504,24,-1,-0.245835504,male,cross,Actinopteri,between
2428,Salmo salar,365,rayyan-697472821,Alternative life histories in the Atlantic salmon: Genetic covariances within the sneaker sexual tactic in males,2011,2004-2006,"Que´bec, Canada",lab,male,male,24,24,NA,NA,4,4,14,14,574,574,animal_model,half_sib,no,narrow,authors,both,non_adult,July length,Timing of early sexual maturity (number of days after hatched),size,reverse_maturation,include,cor,NA,0.182,se,NA,NA,NA,NA,NA,NA,rayyan-697472821,table s2,size,maturation,family,NA,24,-1,NA,male,cross,Actinopteri,between
2429,Salmo salar,365,rayyan-697472821,Alternative life histories in the Atlantic salmon: Genetic covariances within the sneaker sexual tactic in males,2011,2004-2006,"Que´bec, Canada",lab,male,male,24,24,NA,NA,4,4,14,14,574,574,animal_model,half_sib,no,narrow,authors,both,non_adult,January body mass,Timing of early sexual maturity (number of days after hatched),size,reverse_maturation,include,cor,0.446,0.481,se,NA,NA,NA,NA,NA,NA,rayyan-697472821,table s2,size,maturation,family,0.479695858,24,-1,-0.479695858,male,cross,Actinopteri,between
2430,Salmo salar,365,rayyan-697472821,Alternative life histories in the Atlantic salmon: Genetic covariances within the sneaker sexual tactic in males,2011,2004-2006,"Que´bec, Canada",lab,male,male,24,24,NA,NA,4,4,14,14,574,574,animal_model,half_sib,no,narrow,authors,adult,non_adult,November length,Timing of early sexual maturity (number of days after hatched),size,reverse_maturation,include,cor,NA,0.076,se,NA,NA,NA,NA,NA,NA,rayyan-697472821,table s2,size,maturation,family,NA,24,-1,NA,male,cross,Actinopteri,between
2431,Salmo salar,365,rayyan-697472821,Alternative life histories in the Atlantic salmon: Genetic covariances within the sneaker sexual tactic in males,2011,2004-2006,"Que´bec, Canada",lab,male,male,24,24,NA,NA,4,4,14,14,574,574,animal_model,half_sib,no,narrow,authors,adult,non_adult,November body depth,Timing of early sexual maturity (number of days after hatched),size,reverse_maturation,include,cor,0.888,0.129,se,NA,NA,NA,NA,NA,NA,rayyan-697472821,table s2,size,maturation,family,1.412387238,24,-1,-1.412387238,male,cross,Actinopteri,between
2432,Salmo salar,365,rayyan-697472821,Alternative life histories in the Atlantic salmon: Genetic covariances within the sneaker sexual tactic in males,2011,2004-2006,"Que´bec, Canada",lab,male,male,24,24,NA,NA,4,4,14,14,574,574,animal_model,half_sib,no,narrow,authors,both,non_adult,April body mass,Timing of early sexual maturity (number of days after hatched),size,reverse_maturation,include,cor,0.28,0.419,se,NA,NA,NA,NA,NA,NA,rayyan-697472821,table s2,size,maturation,family,0.287682072,24,-1,-0.287682072,male,cross,Actinopteri,between
2433,Salmo salar,365,rayyan-697472821,Alternative life histories in the Atlantic salmon: Genetic covariances within the sneaker sexual tactic in males,2011,2004-2006,"Que´bec, Canada",lab,male,male,24,24,NA,NA,4,4,14,14,574,574,animal_model,half_sib,no,narrow,authors,both,non_adult,July body depth,Timing of early sexual maturity (number of days after hatched),size,reverse_maturation,include,cor,NA,0.092,se,NA,NA,NA,NA,NA,NA,rayyan-697472821,table s2,size,maturation,family,NA,24,-1,NA,male,cross,Actinopteri,between
2434,Salmo salar,365,rayyan-697472821,Alternative life histories in the Atlantic salmon: Genetic covariances within the sneaker sexual tactic in males,2011,2004-2006,"Que´bec, Canada",lab,male,male,24,24,NA,NA,4,4,14,14,574,574,animal_model,half_sib,no,narrow,authors,both,non_adult,January length,Timing of early sexual maturity (number of days after hatched),size,reverse_maturation,include,cor,0.454,0.404,se,NA,NA,NA,NA,NA,NA,rayyan-697472821,table s2,size,maturation,family,0.489727341,24,-1,-0.489727341,male,cross,Actinopteri,between
2435,Salmo salar,365,rayyan-697472821,Alternative life histories in the Atlantic salmon: Genetic covariances within the sneaker sexual tactic in males,2011,2004-2006,"Que´bec, Canada",lab,male,male,24,24,NA,NA,4,4,14,14,574,574,animal_model,half_sib,no,narrow,authors,adult,non_adult,emergence body mass,Timing of early sexual maturity (number of days after hatched),size,reverse_maturation,include,cor,0.485,0.346,se,NA,NA,NA,NA,NA,NA,rayyan-697472821,table s2,size,maturation,family,0.529501575,24,-1,-0.529501575,male,cross,Actinopteri,between
2436,Salmo salar,365,rayyan-697472821,Alternative life histories in the Atlantic salmon: Genetic covariances within the sneaker sexual tactic in males,2011,2004-2006,"Que´bec, Canada",lab,male,male,24,24,NA,NA,4,4,14,14,574,574,animal_model,half_sib,no,narrow,authors,adult,non_adult,November body mass,Timing of early sexual maturity (number of days after hatched),size,reverse_maturation,include,cor,NA,0.064,se,NA,NA,NA,NA,NA,NA,rayyan-697472821,table s2,size,maturation,family,NA,24,-1,NA,male,cross,Actinopteri,between
2437,Salmo salar,365,rayyan-697472821,Alternative life histories in the Atlantic salmon: Genetic covariances within the sneaker sexual tactic in males,2011,2004-2006,"Que´bec, Canada",lab,male,male,24,24,NA,NA,4,4,14,14,574,574,animal_model,half_sib,no,narrow,authors,adult,non_adult,emergence body depth,Timing of early sexual maturity (number of days after hatched),size,reverse_maturation,include,cor,0.25,0.404,se,NA,NA,NA,NA,NA,NA,rayyan-697472821,table s2,size,maturation,family,0.255412812,24,-1,-0.255412812,male,cross,Actinopteri,between
2438,Salmo trutta,244,rayyan-197247410,Individual variation in early life-history traits in brown trout,2000,NA,NA,lab,both,both,20,20,NA,NA,2,2,10,10,400,400,animal_model,half_sib,no,narrow,authors,non_adult,non_adult,yolk sac volume,egg size,size,size,include,cor,0.508,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-197247410,table 3,size,size,family,0.560030416,20,1,0.560030416,both,non_adult,Actinopteri,within
2439,Salmo trutta,244,rayyan-197247410,Individual variation in early life-history traits in brown trout,2000,NA,NA,lab,both,both,20,20,NA,NA,2,2,10,10,400,400,animal_model,half_sib,no,narrow,authors,both,non_adult,lifespan (hatching to death),egg size,survival,size,include,cor,0.1,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-197247410,table 3,survival,size,family,0.100335348,20,1,0.100335348,both,cross,Actinopteri,between
2440,Salmo trutta,244,rayyan-197247410,Individual variation in early life-history traits in brown trout,2000,NA,NA,lab,both,both,20,20,NA,NA,2,2,10,10,400,400,animal_model,half_sib,no,narrow,authors,non_adult,non_adult,development time (fertilization to hatching),yolk sac volume,reverse_maturation,size,include,cor,0.031,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-197247410,table 3,maturation,size,family,0.031009936,20,-1,-0.031009936,both,non_adult,Actinopteri,between
2441,Salmo trutta,244,rayyan-197247410,Individual variation in early life-history traits in brown trout,2000,NA,NA,lab,both,both,20,20,NA,NA,2,2,10,10,400,400,animal_model,half_sib,no,narrow,authors,non_adult,non_adult,development time (fertilization to hatching),length at hatching,reverse_maturation,size,include,cor,0.449,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-197247410,table 3,maturation,size,family,0.483447067,20,-1,-0.483447067,both,non_adult,Actinopteri,between
2442,Salmo trutta,244,rayyan-197247410,Individual variation in early life-history traits in brown trout,2000,NA,NA,lab,both,both,20,20,NA,NA,2,2,10,10,400,400,animal_model,half_sib,no,narrow,authors,non_adult,non_adult,length at hatching,egg size,size,size,include,cor,NA,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-197247410,table 3,size,size,family,NA,20,1,NA,both,non_adult,Actinopteri,within
2443,Salmo trutta,244,rayyan-197247410,Individual variation in early life-history traits in brown trout,2000,NA,NA,lab,both,both,20,20,NA,NA,2,2,10,10,400,400,animal_model,half_sib,no,narrow,authors,both,non_adult,lifespan (hatching to death),yolk sac volume,survival,size,include,cor,0.011,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-197247410,table 3,survival,size,family,0.011000444,20,1,0.011000444,both,cross,Actinopteri,between
2444,Salmo trutta,244,rayyan-197247410,Individual variation in early life-history traits in brown trout,2000,NA,NA,lab,both,both,20,20,NA,NA,2,2,10,10,400,400,animal_model,half_sib,no,narrow,authors,both,non_adult,length at death,egg size,size,size,include,cor,NA,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-197247410,table 3,size,size,family,NA,20,1,NA,both,cross,Actinopteri,within
2445,Salmo trutta,244,rayyan-197247410,Individual variation in early life-history traits in brown trout,2000,NA,NA,lab,both,both,20,20,NA,NA,2,2,10,10,400,400,animal_model,half_sib,no,narrow,authors,both,non_adult,length at death,development time (fertilization to hatching),size,reverse_maturation,include,cor,-0.013,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-197247410,table 3,size,maturation,family,-0.013000732,20,-1,0.013000732,both,cross,Actinopteri,between
2446,Salmo trutta,244,rayyan-197247410,Individual variation in early life-history traits in brown trout,2000,NA,NA,lab,both,both,20,20,NA,NA,2,2,10,10,400,400,animal_model,half_sib,no,narrow,authors,non_adult,non_adult,development time (fertilization to hatching),egg size,reverse_maturation,size,include,cor,0.152,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-197247410,table 3,maturation,size,family,0.153187103,20,-1,-0.153187103,both,non_adult,Actinopteri,between
2447,Salmo trutta,244,rayyan-197247410,Individual variation in early life-history traits in brown trout,2000,NA,NA,lab,both,both,20,20,NA,NA,2,2,10,10,400,400,animal_model,half_sib,no,narrow,authors,both,both,growth rate (hatching to death),length at death,growth,size,include,cor,NA,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-197247410,table 3,growth,size,family,NA,20,1,NA,both,both,Actinopteri,between
2448,Salmo trutta,244,rayyan-197247410,Individual variation in early life-history traits in brown trout,2000,NA,NA,lab,both,both,20,20,NA,NA,2,2,10,10,400,400,animal_model,half_sib,no,narrow,authors,both,non_adult,length at death,yolk sac volume,size,size,include,cor,0.282,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-197247410,table 3,size,size,family,0.289853534,20,1,0.289853534,both,cross,Actinopteri,within
2449,Salmo trutta,244,rayyan-197247410,Individual variation in early life-history traits in brown trout,2000,NA,NA,lab,both,both,20,20,NA,NA,2,2,10,10,400,400,animal_model,half_sib,no,narrow,authors,both,non_adult,lifespan (hatching to death),development time (fertilization to hatching),survival,reverse_maturation,include,cor,-0.026,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-197247410,table 3,survival,maturation,family,-0.026005861,20,-1,0.026005861,both,cross,Actinopteri,between
2450,Salmo trutta,244,rayyan-197247410,Individual variation in early life-history traits in brown trout,2000,NA,NA,lab,both,both,20,20,NA,NA,2,2,10,10,400,400,animal_model,half_sib,no,narrow,authors,both,non_adult,growth rate (hatching to death),length at hatching,growth,size,include,cor,NA,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-197247410,table 3,growth,size,family,NA,20,1,NA,both,cross,Actinopteri,between
2451,Salmo trutta,244,rayyan-197247410,Individual variation in early life-history traits in brown trout,2000,NA,NA,lab,both,both,20,20,NA,NA,2,2,10,10,400,400,animal_model,half_sib,no,narrow,authors,non_adult,non_adult,yolk sac volume,length at hatching,size,size,include,cor,0.49,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-197247410,table 3,size,size,family,0.536060337,20,1,0.536060337,both,non_adult,Actinopteri,within
2452,Salmo trutta,244,rayyan-197247410,Individual variation in early life-history traits in brown trout,2000,NA,NA,lab,both,both,20,20,NA,NA,2,2,10,10,400,400,animal_model,half_sib,no,narrow,authors,both,non_adult,lifespan (hatching to death),length at hatching,survival,size,include,cor,-0.085,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-197247410,table 3,survival,size,family,-0.0852056,20,1,-0.0852056,both,cross,Actinopteri,between
2453,Salmo trutta,244,rayyan-197247410,Individual variation in early life-history traits in brown trout,2000,NA,NA,lab,both,both,20,20,NA,NA,2,2,10,10,400,400,animal_model,half_sib,no,narrow,authors,both,non_adult,growth rate (hatching to death),egg size,growth,size,include,cor,0.64,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-197247410,table 3,growth,size,family,0.758173745,20,1,0.758173745,both,cross,Actinopteri,between
2454,Salmo trutta,244,rayyan-197247410,Individual variation in early life-history traits in brown trout,2000,NA,NA,lab,both,both,20,20,NA,NA,2,2,10,10,400,400,animal_model,half_sib,no,narrow,authors,both,both,length at death,lifespan (hatching to death),size,survival,include,cor,0.105,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-197247410,table 3,size,survival,family,0.105388448,20,1,0.105388448,both,both,Actinopteri,between
2455,Salmo trutta,244,rayyan-197247410,Individual variation in early life-history traits in brown trout,2000,NA,NA,lab,both,both,20,20,NA,NA,2,2,10,10,400,400,animal_model,half_sib,no,narrow,authors,both,both,growth rate (hatching to death),lifespan (hatching to death),growth,survival,include,cor,NA,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-197247410,table 3,growth,survival,family,NA,20,1,NA,both,both,Actinopteri,between
2456,Salmo trutta,244,rayyan-197247410,Individual variation in early life-history traits in brown trout,2000,NA,NA,lab,both,both,20,20,NA,NA,2,2,10,10,400,400,animal_model,half_sib,no,narrow,authors,both,non_adult,growth rate (hatching to death),development time (fertilization to hatching),growth,reverse_maturation,include,cor,0.454,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-197247410,table 3,growth,maturation,family,0.489727341,20,-1,-0.489727341,both,cross,Actinopteri,between
2457,Salmo trutta,244,rayyan-197247410,Individual variation in early life-history traits in brown trout,2000,NA,NA,lab,both,both,20,20,NA,NA,2,2,10,10,400,400,animal_model,half_sib,no,narrow,authors,both,non_adult,length at death,length at hatching,size,size,include,cor,NA,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-197247410,table 3,size,size,family,NA,20,1,NA,both,cross,Actinopteri,within
2458,Salmo trutta,244,rayyan-197247410,Individual variation in early life-history traits in brown trout,2000,NA,NA,lab,both,both,20,20,NA,NA,2,2,10,10,400,400,animal_model,half_sib,no,narrow,authors,both,non_adult,growth rate (hatching to death),yolk sac volume,growth,size,include,cor,0.123,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-197247410,table 3,growth,size,family,0.123625981,20,1,0.123625981,both,cross,Actinopteri,between
2459,Scathophaga stercoraria,405,rayyan-697473033,"Adaptive phenotypic plasticity in growth, development, and body size in the yellow dung fly",1998,1995-1996,"Fehraltorf, Switzerland",lab,female,female,8,8,NA,NA,8,8,8,8,119,119,animal_model,full_sib,no,broad,authors,non_adult,adult,development time,adult body size,reverse_maturation,size,include,cor,0.2,0.07,se,NA,NA,NA,NA,NA,NA,all_female_rg,table 5,maturation,size,family,0.202732554,8,-1,-0.202732554,female,cross,Insecta,between
2460,Scathophaga stercoraria,230,rayyan-197247331,The quantitative genetics of two life history trade-offs in the yellow dung fly in abundant and limited food environments,2005,1995,Fehraltorf,lab,female,female,38,38,NA,NA,38,38,NA,NA,154,154,family_mean_correlation,full_sib,no,broad,authors,adult,non_adult,hind tibia length,developmental time,size,reverse_maturation,include,cor,0.27,NA,NA,NA,NA,NA,NA,NA,NA,med-female,figure 1,size,maturation,family,0.276863823,38,-1,-0.276863823,female,cross,Insecta,between
2461,Scathophaga stercoraria,230,rayyan-197247331,The quantitative genetics of two life history trade-offs in the yellow dung fly in abundant and limited food environments,2005,1995,Fehraltorf,lab,female,female,33,33,NA,NA,33,33,NA,NA,129,129,family_mean_correlation,full_sib,no,broad,authors,adult,non_adult,hind tibia length,developmental time,size,reverse_maturation,include,cor,0.32,NA,NA,NA,NA,NA,NA,NA,NA,low-female,figure 1,size,maturation,family,0.331647109,33,-1,-0.331647109,female,cross,Insecta,between
2462,Scathophaga stercoraria,230,rayyan-197247331,The quantitative genetics of two life history trade-offs in the yellow dung fly in abundant and limited food environments,2005,1995,Fehraltorf,lab,male,male,37,37,NA,NA,37,37,NA,NA,128,128,family_mean_correlation,full_sib,no,broad,authors,adult,non_adult,hind tibia length,developmental time,size,reverse_maturation,include,cor,0.38,NA,NA,NA,NA,NA,NA,NA,NA,high-male,figure 1,size,maturation,family,0.40005965,37,-1,-0.40005965,male,cross,Insecta,between
2463,Scathophaga stercoraria,230,rayyan-197247331,The quantitative genetics of two life history trade-offs in the yellow dung fly in abundant and limited food environments,2005,1995,Fehraltorf,lab,male,male,37,37,NA,NA,37,37,NA,NA,98,98,family_mean_correlation,full_sib,no,broad,authors,adult,non_adult,hind tibia length,developmental time,size,reverse_maturation,include,cor,0.48,NA,NA,NA,NA,NA,NA,NA,NA,low-male,figure 1,size,maturation,family,0.522984278,37,-1,-0.522984278,male,cross,Insecta,between
2467,Scathophaga stercoraria,230,rayyan-197247331,The quantitative genetics of two life history trade-offs in the yellow dung fly in abundant and limited food environments,2005,1995,Fehraltorf,lab,male,male,37,37,NA,NA,37,37,NA,NA,133,133,family_mean_correlation,full_sib,no,broad,authors,adult,non_adult,hind tibia length,developmental time,size,reverse_maturation,include,cor,0.21,NA,NA,NA,NA,NA,NA,NA,NA,med-male,figure 1,size,maturation,family,0.213171347,37,-1,-0.213171347,male,cross,Insecta,between
2476,Scathophaga stercoraria,230,rayyan-197247331,The quantitative genetics of two life history trade-offs in the yellow dung fly in abundant and limited food environments,2005,1995,Fehraltorf,lab,female,female,NA,NA,NA,NA,33,33,11,11,220,220,sire_mean_correlation,half_sib,no,broad,authors,non_adult,adult,egg volume,clutch size,size,fertility,include,cor,-0.16,NA,NA,NA,NA,NA,NA,NA,NA,high_sire_means,figure 2,size,fertility,family,-0.161386696,33,1,-0.161386696,female,cross,Insecta,between
2477,Scathophaga stercoraria,230,rayyan-197247331,The quantitative genetics of two life history trade-offs in the yellow dung fly in abundant and limited food environments,2005,1995,Fehraltorf,lab,female,female,40,40,NA,NA,40,40,NA,NA,171,171,family_mean_correlation,full_sib,no,broad,authors,adult,non_adult,hind tibia length,developmental time,size,reverse_maturation,include,cor,0.22,NA,NA,NA,NA,NA,NA,NA,NA,high-female,figure 1,size,maturation,family,0.223656109,40,-1,-0.223656109,female,cross,Insecta,between
2478,Scathophaga stercoraria,230,rayyan-197247331,The quantitative genetics of two life history trade-offs in the yellow dung fly in abundant and limited food environments,2005,1995,Fehraltorf,lab,female,female,NA,NA,NA,NA,33,33,11,11,220,220,dam_mean_correlation,full_sib,no,broad,authors,non_adult,adult,egg volume,clutch size,size,fertility,include,cor,0.04,NA,NA,NA,NA,NA,NA,NA,NA,high_dam_means,figure 2,size,fertility,family,0.040021354,33,1,0.040021354,female,cross,Insecta,between
2479,Scathophaga stercoraria,230,rayyan-197247331,The quantitative genetics of two life history trade-offs in the yellow dung fly in abundant and limited food environments,2005,1995,Fehraltorf,lab,female,female,NA,NA,NA,NA,48,48,16,16,222,222,dam_mean_correlation,full_sib,no,broad,authors,non_adult,adult,egg volume,clutch size,size,fertility,include,cor,-0.26,NA,NA,NA,NA,NA,NA,NA,NA,low_dam_means,figure 2,size,fertility,family,-0.266108407,48,1,-0.266108407,female,cross,Insecta,between
2480,Scathophaga stercoraria,405,rayyan-697473033,"Adaptive phenotypic plasticity in growth, development, and body size in the yellow dung fly",1998,1995-1996,"Fehraltorf, Switzerland",lab,male,male,8,8,NA,NA,8,8,8,8,107,107,animal_model,full_sib,no,broad,authors,non_adult,adult,development time,adult body size,reverse_maturation,size,include,cor,0.28,0.07,se,NA,NA,NA,NA,NA,NA,all_male_rg,table 5,maturation,size,family,0.287682072,8,-1,-0.287682072,male,cross,Insecta,between
2484,Scathophaga stercoraria,433,rayyan-697473469,The genetic component of copula duration in the yellow dung fly,1996,1993,Zurich,lab,male,male,131,131,NA,NA,NA,NA,NA,NA,328,328,matrix,full_sib,no,broad,authors,adult,non_adult,adult body size,development time,size,reverse_maturation,include,cor,-0.039,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-697473469,table 5,size,maturation,family,-0.039019791,131,-1,0.039019791,male,cross,Insecta,between
2485,Scathophaga stercoraria,230,rayyan-197247331,The quantitative genetics of two life history trade-offs in the yellow dung fly in abundant and limited food environments,2005,1995,Fehraltorf,lab,female,female,NA,NA,NA,NA,48,48,16,16,222,222,sire_mean_correlation,half_sib,no,broad,authors,non_adult,adult,egg volume,clutch size,size,fertility,include,cor,-0.2,NA,NA,NA,NA,NA,NA,NA,NA,low_sire_means,figure 2,size,fertility,family,-0.202732554,48,1,-0.202732554,female,cross,Insecta,between
2486,Sitobion avenae,343,rayyan-697472641,Genetic basis and selection for life-history trait plasticity on alternative host plants for the cereal aphid Sitobion avenae,2014,2013,"Qinghai, China",lab,female,female,NA,NA,6,6,NA,NA,NA,NA,NA,NA,animal_model,genetic_line,no,broad,authors,non_adult,non_adult,development time 3rd instar,development time 4th instar,reverse_maturation,reverse_maturation,include,cor,0.2112,NA,NA,NA,NA,NA,NA,NA,NA,Qinghai_barley,table 3,maturation,maturation,genotype,0.21442704,6,1,0.21442704,female,non_adult,Insecta,within
2487,Sitobion avenae,343,rayyan-697472641,Genetic basis and selection for life-history trait plasticity on alternative host plants for the cereal aphid Sitobion avenae,2014,2013,"Qinghai, China",lab,female,female,NA,NA,6,6,NA,NA,NA,NA,NA,NA,animal_model,genetic_line,no,broad,authors,non_adult,non_adult,development time 2nd instar,development time 4th instar,reverse_maturation,reverse_maturation,include,cor,0.3761,NA,NA,NA,NA,NA,NA,NA,NA,Qinghai_barley,table 3,maturation,maturation,genotype,0.395509296,6,1,0.395509296,female,non_adult,Insecta,within
2488,Sitobion avenae,343,rayyan-697472641,Genetic basis and selection for life-history trait plasticity on alternative host plants for the cereal aphid Sitobion avenae,2014,2013,"Shaanxi, China",lab,female,female,NA,NA,10,10,NA,NA,NA,NA,NA,NA,animal_model,genetic_line,no,broad,authors,non_adult,non_adult,development time 1st instar,development time 3rd instar,reverse_maturation,reverse_maturation,include,cor,0.0658,NA,NA,NA,NA,NA,NA,NA,NA,Shaanxi_barley,table 3,maturation,maturation,genotype,0.065895211,10,1,0.065895211,female,non_adult,Insecta,within
2489,Sitobion avenae,343,rayyan-697472641,Genetic basis and selection for life-history trait plasticity on alternative host plants for the cereal aphid Sitobion avenae,2014,2013,"Qinghai, China",lab,female,female,NA,NA,6,6,NA,NA,NA,NA,NA,NA,animal_model,genetic_line,no,broad,authors,non_adult,non_adult,development time 2nd instar,development time 5th instar,reverse_maturation,reverse_maturation,include,cor,-0.1324,NA,NA,NA,NA,NA,NA,NA,NA,Qinghai_barley,table 3,maturation,maturation,genotype,-0.133181887,6,1,-0.133181887,female,non_adult,Insecta,within
2490,Sitobion avenae,343,rayyan-697472641,Genetic basis and selection for life-history trait plasticity on alternative host plants for the cereal aphid Sitobion avenae,2014,2013,"Shaanxi, China",lab,female,female,NA,NA,10,10,NA,NA,NA,NA,NA,NA,animal_model,genetic_line,no,broad,authors,non_adult,adult,development time 1st instar,7 day fecundity,reverse_maturation,fertility,include,cor,-0.0489,NA,NA,NA,NA,NA,NA,NA,NA,Shaanxi_barley,table 3,maturation,fertility,genotype,-0.048939033,10,-1,0.048939033,female,cross,Insecta,between
2491,Sitobion avenae,343,rayyan-697472641,Genetic basis and selection for life-history trait plasticity on alternative host plants for the cereal aphid Sitobion avenae,2014,2013,"Qinghai, China",lab,female,female,NA,NA,6,6,NA,NA,NA,NA,NA,NA,animal_model,genetic_line,no,broad,authors,non_adult,adult,development time 1st instar,7 day fecundity,reverse_maturation,fertility,include,cor,0.3816,NA,NA,NA,NA,NA,NA,NA,NA,Qinghai_barley,table 3,maturation,fertility,genotype,0.401931015,6,-1,-0.401931015,female,cross,Insecta,between
2492,Sitobion avenae,343,rayyan-697472641,Genetic basis and selection for life-history trait plasticity on alternative host plants for the cereal aphid Sitobion avenae,2014,2013,"Qinghai, China",lab,female,female,NA,NA,6,6,NA,NA,NA,NA,NA,NA,animal_model,genetic_line,no,broad,authors,non_adult,adult,development time 2nd instar,7 day fecundity,reverse_maturation,fertility,include,cor,-0.1279,NA,NA,NA,NA,NA,NA,NA,NA,Qinghai_barley,table 3,maturation,fertility,genotype,-0.12860434,6,-1,0.12860434,female,cross,Insecta,between
2493,Sitobion avenae,343,rayyan-697472641,Genetic basis and selection for life-history trait plasticity on alternative host plants for the cereal aphid Sitobion avenae,2014,2013,"Qinghai, China",lab,female,female,NA,NA,6,6,NA,NA,NA,NA,NA,NA,animal_model,genetic_line,no,broad,authors,non_adult,non_adult,development time 3rd instar,development time 5th instar,reverse_maturation,reverse_maturation,include,cor,0.62,NA,NA,NA,NA,NA,NA,NA,NA,Qinghai_barley,table 3,maturation,maturation,genotype,0.725005088,6,1,0.725005088,female,non_adult,Insecta,within
2494,Sitobion avenae,343,rayyan-697472641,Genetic basis and selection for life-history trait plasticity on alternative host plants for the cereal aphid Sitobion avenae,2014,2013,"Qinghai, China",lab,female,female,NA,NA,6,6,NA,NA,NA,NA,NA,NA,animal_model,genetic_line,no,broad,authors,non_adult,non_adult,development time 2nd instar,development time 3rd instar,reverse_maturation,reverse_maturation,include,cor,0.1221,NA,NA,NA,NA,NA,NA,NA,NA,Qinghai_barley,table 3,maturation,maturation,genotype,0.122712258,6,1,0.122712258,female,non_adult,Insecta,within
2495,Sitobion avenae,343,rayyan-697472641,Genetic basis and selection for life-history trait plasticity on alternative host plants for the cereal aphid Sitobion avenae,2014,2013,"Shaanxi, China",lab,female,female,NA,NA,10,10,NA,NA,NA,NA,NA,NA,animal_model,genetic_line,no,broad,authors,non_adult,non_adult,development time 4th instar,development time 5th instar,reverse_maturation,reverse_maturation,include,cor,0.558,NA,NA,NA,NA,NA,NA,NA,NA,Shaanxi_wheat,table 3,maturation,maturation,genotype,0.629924172,10,1,0.629924172,female,non_adult,Insecta,within
2496,Sitobion avenae,343,rayyan-697472641,Genetic basis and selection for life-history trait plasticity on alternative host plants for the cereal aphid Sitobion avenae,2014,2013,"Shaanxi, China",lab,female,female,NA,NA,10,10,NA,NA,NA,NA,NA,NA,animal_model,genetic_line,no,broad,authors,non_adult,non_adult,development time 1st instar,development time 2nd instar,reverse_maturation,reverse_maturation,include,cor,-0.0298,NA,NA,NA,NA,NA,NA,NA,NA,Shaanxi_barley,table 3,maturation,maturation,genotype,-0.029808826,10,1,-0.029808826,female,non_adult,Insecta,within
2497,Sitobion avenae,343,rayyan-697472641,Genetic basis and selection for life-history trait plasticity on alternative host plants for the cereal aphid Sitobion avenae,2014,2013,"Shaanxi, China",lab,female,female,NA,NA,10,10,NA,NA,NA,NA,NA,NA,animal_model,genetic_line,no,broad,authors,non_adult,non_adult,development time 3rd instar,development time 5th instar,reverse_maturation,reverse_maturation,include,cor,0.3133,NA,NA,NA,NA,NA,NA,NA,NA,Shaanxi_wheat,table 3,maturation,maturation,genotype,0.324200408,10,1,0.324200408,female,non_adult,Insecta,within
2498,Sitobion avenae,343,rayyan-697472641,Genetic basis and selection for life-history trait plasticity on alternative host plants for the cereal aphid Sitobion avenae,2014,2013,"Shaanxi, China",lab,female,female,NA,NA,10,10,NA,NA,NA,NA,NA,NA,animal_model,genetic_line,no,broad,authors,non_adult,non_adult,development time 1st instar,development time 5th instar,reverse_maturation,reverse_maturation,include,cor,0.0958,NA,NA,NA,NA,NA,NA,NA,NA,Shaanxi_barley,table 3,maturation,maturation,genotype,0.096094697,10,1,0.096094697,female,non_adult,Insecta,within
2499,Sitobion avenae,343,rayyan-697472641,Genetic basis and selection for life-history trait plasticity on alternative host plants for the cereal aphid Sitobion avenae,2014,2013,"Qinghai, China",lab,female,female,NA,NA,6,6,NA,NA,NA,NA,NA,NA,animal_model,genetic_line,no,broad,authors,non_adult,non_adult,development time 1st instar,development time 3rd instar,reverse_maturation,reverse_maturation,include,cor,0.5457,NA,NA,NA,NA,NA,NA,NA,NA,Qinghai_oat,table 3,maturation,maturation,genotype,0.612237194,6,1,0.612237194,female,non_adult,Insecta,within
2500,Sitobion avenae,343,rayyan-697472641,Genetic basis and selection for life-history trait plasticity on alternative host plants for the cereal aphid Sitobion avenae,2014,2013,"Qinghai, China",lab,female,female,NA,NA,6,6,NA,NA,NA,NA,NA,NA,animal_model,genetic_line,no,broad,authors,non_adult,adult,development time 3rd instar,7 day fecundity,reverse_maturation,fertility,include,cor,0.2548,NA,NA,NA,NA,NA,NA,NA,NA,Qinghai_barley,table 3,maturation,fertility,genotype,0.260539419,6,-1,-0.260539419,female,cross,Insecta,between
2501,Sitobion avenae,343,rayyan-697472641,Genetic basis and selection for life-history trait plasticity on alternative host plants for the cereal aphid Sitobion avenae,2014,2013,"Qinghai, China",lab,female,female,NA,NA,6,6,NA,NA,NA,NA,NA,NA,animal_model,genetic_line,no,broad,authors,non_adult,non_adult,development time 1st instar,development time 5th instar,reverse_maturation,reverse_maturation,include,cor,0.3767,NA,NA,NA,NA,NA,NA,NA,NA,Qinghai_oat,table 3,maturation,maturation,genotype,0.396208333,6,1,0.396208333,female,non_adult,Insecta,within
2502,Sitobion avenae,343,rayyan-697472641,Genetic basis and selection for life-history trait plasticity on alternative host plants for the cereal aphid Sitobion avenae,2014,2013,"Qinghai, China",lab,female,female,NA,NA,6,6,NA,NA,NA,NA,NA,NA,animal_model,genetic_line,no,broad,authors,non_adult,adult,development time 1st instar,7 day fecundity,reverse_maturation,fertility,include,cor,0.3511,NA,NA,NA,NA,NA,NA,NA,NA,Qinghai_oat,table 3,maturation,fertility,genotype,0.366697866,6,-1,-0.366697866,female,cross,Insecta,between
2503,Sitobion avenae,343,rayyan-697472641,Genetic basis and selection for life-history trait plasticity on alternative host plants for the cereal aphid Sitobion avenae,2014,2013,"Shaanxi, China",lab,female,female,NA,NA,10,10,NA,NA,NA,NA,NA,NA,animal_model,genetic_line,no,broad,authors,non_adult,adult,development time 3rd instar,7 day fecundity,reverse_maturation,fertility,include,cor,0.0046,NA,NA,NA,NA,NA,NA,NA,NA,Shaanxi_wheat,table 3,maturation,fertility,genotype,0.004600032,10,-1,-0.004600032,female,cross,Insecta,between
2504,Sitobion avenae,343,rayyan-697472641,Genetic basis and selection for life-history trait plasticity on alternative host plants for the cereal aphid Sitobion avenae,2014,2013,"Qinghai, China",lab,female,female,NA,NA,6,6,NA,NA,NA,NA,NA,NA,animal_model,genetic_line,no,broad,authors,non_adult,non_adult,development time 1st instar,development time 4th instar,reverse_maturation,reverse_maturation,include,cor,0.0407,NA,NA,NA,NA,NA,NA,NA,NA,Qinghai_oat,table 3,maturation,maturation,genotype,0.040722495,6,1,0.040722495,female,non_adult,Insecta,within
2505,Sitobion avenae,343,rayyan-697472641,Genetic basis and selection for life-history trait plasticity on alternative host plants for the cereal aphid Sitobion avenae,2014,2013,"Shaanxi, China",lab,female,female,NA,NA,10,10,NA,NA,NA,NA,NA,NA,animal_model,genetic_line,no,broad,authors,non_adult,adult,development time 4th instar,7 day fecundity,reverse_maturation,fertility,include,cor,0.5298,NA,NA,NA,NA,NA,NA,NA,NA,Shaanxi_wheat,table 3,maturation,fertility,genotype,0.589867075,10,-1,-0.589867075,female,cross,Insecta,between
2506,Sitobion avenae,343,rayyan-697472641,Genetic basis and selection for life-history trait plasticity on alternative host plants for the cereal aphid Sitobion avenae,2014,2013,"Qinghai, China",lab,female,female,NA,NA,6,6,NA,NA,NA,NA,NA,NA,animal_model,genetic_line,no,broad,authors,non_adult,adult,development time 5th instar,7 day fecundity,reverse_maturation,fertility,include,cor,0.474,NA,NA,NA,NA,NA,NA,NA,NA,Qinghai_barley,table 3,maturation,fertility,genotype,0.51521693,6,-1,-0.51521693,female,cross,Insecta,between
2507,Sitobion avenae,343,rayyan-697472641,Genetic basis and selection for life-history trait plasticity on alternative host plants for the cereal aphid Sitobion avenae,2014,2013,"Qinghai, China",lab,female,female,NA,NA,6,6,NA,NA,NA,NA,NA,NA,animal_model,genetic_line,no,broad,authors,non_adult,adult,development time 5th instar,7 day fecundity,reverse_maturation,fertility,include,cor,0.4965,NA,NA,NA,NA,NA,NA,NA,NA,Qinghai_oat,table 3,maturation,fertility,genotype,0.544650308,6,-1,-0.544650308,female,cross,Insecta,between
2508,Sitobion avenae,343,rayyan-697472641,Genetic basis and selection for life-history trait plasticity on alternative host plants for the cereal aphid Sitobion avenae,2014,2013,"Qinghai, China",lab,female,female,NA,NA,6,6,NA,NA,NA,NA,NA,NA,animal_model,genetic_line,no,broad,authors,non_adult,non_adult,development time 2nd instar,development time 4th instar,reverse_maturation,reverse_maturation,include,cor,-0.1558,NA,NA,NA,NA,NA,NA,NA,NA,Qinghai_oat,table 3,maturation,maturation,genotype,-0.157079295,6,1,-0.157079295,female,non_adult,Insecta,within
2509,Sitobion avenae,343,rayyan-697472641,Genetic basis and selection for life-history trait plasticity on alternative host plants for the cereal aphid Sitobion avenae,2014,2013,"Qinghai, China",lab,female,female,NA,NA,6,6,NA,NA,NA,NA,NA,NA,animal_model,genetic_line,no,broad,authors,non_adult,adult,development time 4th instar,7 day fecundity,reverse_maturation,fertility,include,cor,0.4789,NA,NA,NA,NA,NA,NA,NA,NA,Qinghai_barley,table 3,maturation,fertility,genotype,0.521555943,6,-1,-0.521555943,female,cross,Insecta,between
2510,Sitobion avenae,343,rayyan-697472641,Genetic basis and selection for life-history trait plasticity on alternative host plants for the cereal aphid Sitobion avenae,2014,2013,"Qinghai, China",lab,female,female,NA,NA,6,6,NA,NA,NA,NA,NA,NA,animal_model,genetic_line,no,broad,authors,non_adult,non_adult,development time 1st instar,development time 3rd instar,reverse_maturation,reverse_maturation,include,cor,-0.0545,NA,NA,NA,NA,NA,NA,NA,NA,Qinghai_wheat,table 3,maturation,maturation,genotype,-0.054554056,6,1,-0.054554056,female,non_adult,Insecta,within
2511,Sitobion avenae,343,rayyan-697472641,Genetic basis and selection for life-history trait plasticity on alternative host plants for the cereal aphid Sitobion avenae,2014,2013,"Qinghai, China",lab,female,female,NA,NA,6,6,NA,NA,NA,NA,NA,NA,animal_model,genetic_line,no,broad,authors,non_adult,non_adult,development time 1st instar,development time 4th instar,reverse_maturation,reverse_maturation,include,cor,0.2627,NA,NA,NA,NA,NA,NA,NA,NA,Qinghai_wheat,table 3,maturation,maturation,genotype,0.26900635,6,1,0.26900635,female,non_adult,Insecta,within
2512,Sitobion avenae,343,rayyan-697472641,Genetic basis and selection for life-history trait plasticity on alternative host plants for the cereal aphid Sitobion avenae,2014,2013,"Shaanxi, China",lab,female,female,NA,NA,10,10,NA,NA,NA,NA,NA,NA,animal_model,genetic_line,no,broad,authors,non_adult,non_adult,development time 2nd instar,development time 4th instar,reverse_maturation,reverse_maturation,include,cor,-0.0985,NA,NA,NA,NA,NA,NA,NA,NA,Shaanxi_oat,table 3,maturation,maturation,genotype,-0.098820425,10,1,-0.098820425,female,non_adult,Insecta,within
2513,Sitobion avenae,343,rayyan-697472641,Genetic basis and selection for life-history trait plasticity on alternative host plants for the cereal aphid Sitobion avenae,2014,2013,"Qinghai, China",lab,female,female,NA,NA,6,6,NA,NA,NA,NA,NA,NA,animal_model,genetic_line,no,broad,authors,non_adult,non_adult,development time 1st instar,development time 2nd instar,reverse_maturation,reverse_maturation,include,cor,0.3974,NA,NA,NA,NA,NA,NA,NA,NA,Qinghai_wheat,table 3,maturation,maturation,genotype,0.42055751,6,1,0.42055751,female,non_adult,Insecta,within
2514,Sitobion avenae,343,rayyan-697472641,Genetic basis and selection for life-history trait plasticity on alternative host plants for the cereal aphid Sitobion avenae,2014,2013,"Qinghai, China",lab,female,female,NA,NA,6,6,NA,NA,NA,NA,NA,NA,animal_model,genetic_line,no,broad,authors,non_adult,non_adult,development time 2nd instar,development time 5th instar,reverse_maturation,reverse_maturation,include,cor,-0.1924,NA,NA,NA,NA,NA,NA,NA,NA,Qinghai_oat,table 3,maturation,maturation,genotype,-0.194828238,6,1,-0.194828238,female,non_adult,Insecta,within
2515,Sitobion avenae,343,rayyan-697472641,Genetic basis and selection for life-history trait plasticity on alternative host plants for the cereal aphid Sitobion avenae,2014,2013,"Shaanxi, China",lab,female,female,NA,NA,10,10,NA,NA,NA,NA,NA,NA,animal_model,genetic_line,no,broad,authors,non_adult,adult,development time 5th instar,7 day fecundity,reverse_maturation,fertility,include,cor,0.1787,NA,NA,NA,NA,NA,NA,NA,NA,Shaanxi_wheat,table 3,maturation,fertility,genotype,0.180639482,10,-1,-0.180639482,female,cross,Insecta,between
2516,Sitobion avenae,343,rayyan-697472641,Genetic basis and selection for life-history trait plasticity on alternative host plants for the cereal aphid Sitobion avenae,2014,2013,"Qinghai, China",lab,female,female,NA,NA,6,6,NA,NA,NA,NA,NA,NA,animal_model,genetic_line,no,broad,authors,non_adult,non_adult,development time 2nd instar,development time 3rd instar,reverse_maturation,reverse_maturation,include,cor,-0.1156,NA,NA,NA,NA,NA,NA,NA,NA,Qinghai_oat,table 3,maturation,maturation,genotype,-0.116119103,6,1,-0.116119103,female,non_adult,Insecta,within
2517,Sitobion avenae,343,rayyan-697472641,Genetic basis and selection for life-history trait plasticity on alternative host plants for the cereal aphid Sitobion avenae,2014,2013,"Qinghai, China",lab,female,female,NA,NA,6,6,NA,NA,NA,NA,NA,NA,animal_model,genetic_line,no,broad,authors,non_adult,adult,development time 1st instar,7 day fecundity,reverse_maturation,fertility,include,cor,0.0926,NA,NA,NA,NA,NA,NA,NA,NA,Qinghai_wheat,table 3,maturation,fertility,genotype,0.092866044,6,-1,-0.092866044,female,cross,Insecta,between
2518,Sitobion avenae,343,rayyan-697472641,Genetic basis and selection for life-history trait plasticity on alternative host plants for the cereal aphid Sitobion avenae,2014,2013,"Qinghai, China",lab,female,female,NA,NA,6,6,NA,NA,NA,NA,NA,NA,animal_model,genetic_line,no,broad,authors,non_adult,adult,development time 3rd instar,7 day fecundity,reverse_maturation,fertility,include,cor,0.2546,NA,NA,NA,NA,NA,NA,NA,NA,Qinghai_oat,table 3,maturation,fertility,genotype,0.260325544,6,-1,-0.260325544,female,cross,Insecta,between
2519,Sitobion avenae,343,rayyan-697472641,Genetic basis and selection for life-history trait plasticity on alternative host plants for the cereal aphid Sitobion avenae,2014,2013,"Qinghai, China",lab,female,female,NA,NA,6,6,NA,NA,NA,NA,NA,NA,animal_model,genetic_line,no,broad,authors,non_adult,non_adult,development time 4th instar,development time 5th instar,reverse_maturation,reverse_maturation,include,cor,0.4431,NA,NA,NA,NA,NA,NA,NA,NA,Qinghai_oat,table 3,maturation,maturation,genotype,0.476081583,6,1,0.476081583,female,non_adult,Insecta,within
2520,Sitobion avenae,343,rayyan-697472641,Genetic basis and selection for life-history trait plasticity on alternative host plants for the cereal aphid Sitobion avenae,2014,2013,"Qinghai, China",lab,female,female,NA,NA,6,6,NA,NA,NA,NA,NA,NA,animal_model,genetic_line,no,broad,authors,non_adult,non_adult,development time 1st instar,development time 2nd instar,reverse_maturation,reverse_maturation,include,cor,0.0492,NA,NA,NA,NA,NA,NA,NA,NA,Qinghai_oat,table 3,maturation,maturation,genotype,0.049239756,6,1,0.049239756,female,non_adult,Insecta,within
2521,Sitobion avenae,343,rayyan-697472641,Genetic basis and selection for life-history trait plasticity on alternative host plants for the cereal aphid Sitobion avenae,2014,2013,"Qinghai, China",lab,female,female,NA,NA,6,6,NA,NA,NA,NA,NA,NA,animal_model,genetic_line,no,broad,authors,non_adult,non_adult,development time 4th instar,development time 5th instar,reverse_maturation,reverse_maturation,include,cor,0.4312,NA,NA,NA,NA,NA,NA,NA,NA,Qinghai_wheat,table 3,maturation,maturation,genotype,0.461369827,6,1,0.461369827,female,non_adult,Insecta,within
2522,Sitobion avenae,343,rayyan-697472641,Genetic basis and selection for life-history trait plasticity on alternative host plants for the cereal aphid Sitobion avenae,2014,2013,"Qinghai, China",lab,female,female,NA,NA,6,6,NA,NA,NA,NA,NA,NA,animal_model,genetic_line,no,broad,authors,non_adult,adult,development time 4th instar,7 day fecundity,reverse_maturation,fertility,include,cor,0.1668,NA,NA,NA,NA,NA,NA,NA,NA,Qinghai_wheat,table 3,maturation,fertility,genotype,0.168373264,6,-1,-0.168373264,female,cross,Insecta,between
2523,Sitobion avenae,343,rayyan-697472641,Genetic basis and selection for life-history trait plasticity on alternative host plants for the cereal aphid Sitobion avenae,2014,2013,"Qinghai, China",lab,female,female,NA,NA,6,6,NA,NA,NA,NA,NA,NA,animal_model,genetic_line,no,broad,authors,non_adult,adult,development time 5th instar,7 day fecundity,reverse_maturation,fertility,include,cor,0.5531,NA,NA,NA,NA,NA,NA,NA,NA,Qinghai_wheat,table 3,maturation,fertility,genotype,0.622836678,6,-1,-0.622836678,female,cross,Insecta,between
2524,Sitobion avenae,343,rayyan-697472641,Genetic basis and selection for life-history trait plasticity on alternative host plants for the cereal aphid Sitobion avenae,2014,2013,"Qinghai, China",lab,female,female,NA,NA,6,6,NA,NA,NA,NA,NA,NA,animal_model,genetic_line,no,broad,authors,non_adult,non_adult,development time 1st instar,development time 5th instar,reverse_maturation,reverse_maturation,include,cor,0.3264,NA,NA,NA,NA,NA,NA,NA,NA,Qinghai_barley,table 3,maturation,maturation,genotype,0.338793661,6,1,0.338793661,female,non_adult,Insecta,within
2525,Sitobion avenae,343,rayyan-697472641,Genetic basis and selection for life-history trait plasticity on alternative host plants for the cereal aphid Sitobion avenae,2014,2013,"Shaanxi, China",lab,female,female,NA,NA,10,10,NA,NA,NA,NA,NA,NA,animal_model,genetic_line,no,broad,authors,non_adult,adult,development time 2nd instar,7 day fecundity,reverse_maturation,fertility,include,cor,0.156,NA,NA,NA,NA,NA,NA,NA,NA,Shaanxi_wheat,table 3,maturation,fertility,genotype,0.157284277,10,-1,-0.157284277,female,cross,Insecta,between
2526,Sitobion avenae,343,rayyan-697472641,Genetic basis and selection for life-history trait plasticity on alternative host plants for the cereal aphid Sitobion avenae,2014,2013,"Shaanxi, China",lab,female,female,NA,NA,10,10,NA,NA,NA,NA,NA,NA,animal_model,genetic_line,no,broad,authors,non_adult,non_adult,development time 3rd instar,development time 4th instar,reverse_maturation,reverse_maturation,include,cor,0.3118,NA,NA,NA,NA,NA,NA,NA,NA,Shaanxi_wheat,table 3,maturation,maturation,genotype,0.322538013,10,1,0.322538013,female,non_adult,Insecta,within
2527,Sitobion avenae,343,rayyan-697472641,Genetic basis and selection for life-history trait plasticity on alternative host plants for the cereal aphid Sitobion avenae,2014,2013,"Shaanxi, China",lab,female,female,NA,NA,10,10,NA,NA,NA,NA,NA,NA,animal_model,genetic_line,no,broad,authors,non_adult,non_adult,development time 1st instar,development time 4th instar,reverse_maturation,reverse_maturation,include,cor,0.0308,NA,NA,NA,NA,NA,NA,NA,NA,Shaanxi_barley,table 3,maturation,maturation,genotype,0.030809745,10,1,0.030809745,female,non_adult,Insecta,within
2528,Sitobion avenae,343,rayyan-697472641,Genetic basis and selection for life-history trait plasticity on alternative host plants for the cereal aphid Sitobion avenae,2014,2013,"Shaanxi, China",lab,female,female,NA,NA,10,10,NA,NA,NA,NA,NA,NA,animal_model,genetic_line,no,broad,authors,non_adult,non_adult,development time 1st instar,development time 2nd instar,reverse_maturation,reverse_maturation,include,cor,0.2332,NA,NA,NA,NA,NA,NA,NA,NA,Shaanxi_oat,table 3,maturation,maturation,genotype,0.237570842,10,1,0.237570842,female,non_adult,Insecta,within
2529,Sitobion avenae,343,rayyan-697472641,Genetic basis and selection for life-history trait plasticity on alternative host plants for the cereal aphid Sitobion avenae,2014,2013,"Qinghai, China",lab,female,female,NA,NA,6,6,NA,NA,NA,NA,NA,NA,animal_model,genetic_line,no,broad,authors,non_adult,non_adult,development time 2nd instar,development time 5th instar,reverse_maturation,reverse_maturation,include,cor,0.267,NA,NA,NA,NA,NA,NA,NA,NA,Qinghai_wheat,table 3,maturation,maturation,genotype,0.273630739,6,1,0.273630739,female,non_adult,Insecta,within
2530,Sitobion avenae,343,rayyan-697472641,Genetic basis and selection for life-history trait plasticity on alternative host plants for the cereal aphid Sitobion avenae,2014,2013,"Qinghai, China",lab,female,female,NA,NA,6,6,NA,NA,NA,NA,NA,NA,animal_model,genetic_line,no,broad,authors,non_adult,adult,development time 2nd instar,7 day fecundity,reverse_maturation,fertility,include,cor,0.1822,NA,NA,NA,NA,NA,NA,NA,NA,Qinghai_wheat,table 3,maturation,fertility,genotype,0.18425729,6,-1,-0.18425729,female,cross,Insecta,between
2531,Sitobion avenae,343,rayyan-697472641,Genetic basis and selection for life-history trait plasticity on alternative host plants for the cereal aphid Sitobion avenae,2014,2013,"Qinghai, China",lab,female,female,NA,NA,6,6,NA,NA,NA,NA,NA,NA,animal_model,genetic_line,no,broad,authors,non_adult,non_adult,development time 3rd instar,development time 4th instar,reverse_maturation,reverse_maturation,include,cor,0.156,NA,NA,NA,NA,NA,NA,NA,NA,Qinghai_wheat,table 3,maturation,maturation,genotype,0.157284277,6,1,0.157284277,female,non_adult,Insecta,within
2532,Sitobion avenae,343,rayyan-697472641,Genetic basis and selection for life-history trait plasticity on alternative host plants for the cereal aphid Sitobion avenae,2014,2013,"Shaanxi, China",lab,female,female,NA,NA,10,10,NA,NA,NA,NA,NA,NA,animal_model,genetic_line,no,broad,authors,non_adult,non_adult,development time 2nd instar,development time 4th instar,reverse_maturation,reverse_maturation,include,cor,0.1614,NA,NA,NA,NA,NA,NA,NA,NA,Shaanxi_barley,table 3,maturation,maturation,genotype,0.162823809,10,1,0.162823809,female,non_adult,Insecta,within
2533,Sitobion avenae,343,rayyan-697472641,Genetic basis and selection for life-history trait plasticity on alternative host plants for the cereal aphid Sitobion avenae,2014,2013,"Shaanxi, China",lab,female,female,NA,NA,10,10,NA,NA,NA,NA,NA,NA,animal_model,genetic_line,no,broad,authors,non_adult,non_adult,development time 2nd instar,development time 5th instar,reverse_maturation,reverse_maturation,include,cor,0.2843,NA,NA,NA,NA,NA,NA,NA,NA,Shaanxi_barley,table 3,maturation,maturation,genotype,0.292354009,10,1,0.292354009,female,non_adult,Insecta,within
2534,Sitobion avenae,343,rayyan-697472641,Genetic basis and selection for life-history trait plasticity on alternative host plants for the cereal aphid Sitobion avenae,2014,2013,"Shaanxi, China",lab,female,female,NA,NA,10,10,NA,NA,NA,NA,NA,NA,animal_model,genetic_line,no,broad,authors,non_adult,adult,development time 2nd instar,7 day fecundity,reverse_maturation,fertility,include,cor,-0.3327,NA,NA,NA,NA,NA,NA,NA,NA,Shaanxi_barley,table 3,maturation,fertility,genotype,-0.345861259,10,-1,0.345861259,female,cross,Insecta,between
2535,Sitobion avenae,343,rayyan-697472641,Genetic basis and selection for life-history trait plasticity on alternative host plants for the cereal aphid Sitobion avenae,2014,2013,"Shaanxi, China",lab,female,female,NA,NA,10,10,NA,NA,NA,NA,NA,NA,animal_model,genetic_line,no,broad,authors,non_adult,non_adult,development time 3rd instar,development time 4th instar,reverse_maturation,reverse_maturation,include,cor,0.8745,NA,NA,NA,NA,NA,NA,NA,NA,Shaanxi_barley,table 3,maturation,maturation,genotype,1.351895739,10,1,1.351895739,female,non_adult,Insecta,within
2536,Sitobion avenae,343,rayyan-697472641,Genetic basis and selection for life-history trait plasticity on alternative host plants for the cereal aphid Sitobion avenae,2014,2013,"Shaanxi, China",lab,female,female,NA,NA,10,10,NA,NA,NA,NA,NA,NA,animal_model,genetic_line,no,broad,authors,non_adult,non_adult,development time 3rd instar,development time 5th instar,reverse_maturation,reverse_maturation,include,cor,0.8429,NA,NA,NA,NA,NA,NA,NA,NA,Shaanxi_barley,table 3,maturation,maturation,genotype,1.231106576,10,1,1.231106576,female,non_adult,Insecta,within
2537,Sitobion avenae,343,rayyan-697472641,Genetic basis and selection for life-history trait plasticity on alternative host plants for the cereal aphid Sitobion avenae,2014,2013,"Shaanxi, China",lab,female,female,NA,NA,10,10,NA,NA,NA,NA,NA,NA,animal_model,genetic_line,no,broad,authors,non_adult,adult,development time 3rd instar,7 day fecundity,reverse_maturation,fertility,include,cor,0.2577,NA,NA,NA,NA,NA,NA,NA,NA,Shaanxi_barley,table 3,maturation,fertility,genotype,0.26364323,10,-1,-0.26364323,female,cross,Insecta,between
2538,Sitobion avenae,343,rayyan-697472641,Genetic basis and selection for life-history trait plasticity on alternative host plants for the cereal aphid Sitobion avenae,2014,2013,"Shaanxi, China",lab,female,female,NA,NA,10,10,NA,NA,NA,NA,NA,NA,animal_model,genetic_line,no,broad,authors,non_adult,non_adult,development time 4th instar,development time 5th instar,reverse_maturation,reverse_maturation,include,cor,0.8271,NA,NA,NA,NA,NA,NA,NA,NA,Shaanxi_barley,table 3,maturation,maturation,genotype,1.178885948,10,1,1.178885948,female,non_adult,Insecta,within
2539,Sitobion avenae,343,rayyan-697472641,Genetic basis and selection for life-history trait plasticity on alternative host plants for the cereal aphid Sitobion avenae,2014,2013,"Shaanxi, China",lab,female,female,NA,NA,10,10,NA,NA,NA,NA,NA,NA,animal_model,genetic_line,no,broad,authors,non_adult,adult,development time 4th instar,7 day fecundity,reverse_maturation,fertility,include,cor,0.4057,NA,NA,NA,NA,NA,NA,NA,NA,Shaanxi_barley,table 3,maturation,fertility,genotype,0.430453218,10,-1,-0.430453218,female,cross,Insecta,between
2540,Sitobion avenae,343,rayyan-697472641,Genetic basis and selection for life-history trait plasticity on alternative host plants for the cereal aphid Sitobion avenae,2014,2013,"Shaanxi, China",lab,female,female,NA,NA,10,10,NA,NA,NA,NA,NA,NA,animal_model,genetic_line,no,broad,authors,non_adult,adult,development time 5th instar,7 day fecundity,reverse_maturation,fertility,include,cor,0.4536,NA,NA,NA,NA,NA,NA,NA,NA,Shaanxi_barley,table 3,maturation,fertility,genotype,0.489223604,10,-1,-0.489223604,female,cross,Insecta,between
2541,Sitobion avenae,343,rayyan-697472641,Genetic basis and selection for life-history trait plasticity on alternative host plants for the cereal aphid Sitobion avenae,2014,2013,"Qinghai, China",lab,female,female,NA,NA,6,6,NA,NA,NA,NA,NA,NA,animal_model,genetic_line,no,broad,authors,non_adult,non_adult,development time 2nd instar,development time 3rd instar,reverse_maturation,reverse_maturation,include,cor,-0.1479,NA,NA,NA,NA,NA,NA,NA,NA,Qinghai_wheat,table 3,maturation,maturation,genotype,-0.148992787,6,1,-0.148992787,female,non_adult,Insecta,within
2542,Sitobion avenae,343,rayyan-697472641,Genetic basis and selection for life-history trait plasticity on alternative host plants for the cereal aphid Sitobion avenae,2014,2013,"Qinghai, China",lab,female,female,NA,NA,6,6,NA,NA,NA,NA,NA,NA,animal_model,genetic_line,no,broad,authors,non_adult,non_adult,development time 2nd instar,development time 4th instar,reverse_maturation,reverse_maturation,include,cor,0.3252,NA,NA,NA,NA,NA,NA,NA,NA,Qinghai_wheat,table 3,maturation,maturation,genotype,0.33745116,6,1,0.33745116,female,non_adult,Insecta,within
2543,Sitobion avenae,343,rayyan-697472641,Genetic basis and selection for life-history trait plasticity on alternative host plants for the cereal aphid Sitobion avenae,2014,2013,"Shaanxi, China",lab,female,female,NA,NA,10,10,NA,NA,NA,NA,NA,NA,animal_model,genetic_line,no,broad,authors,non_adult,adult,development time 5th instar,7 day fecundity,reverse_maturation,fertility,include,cor,0.2848,NA,NA,NA,NA,NA,NA,NA,NA,Shaanxi_oat,table 3,maturation,fertility,genotype,0.29289806,10,-1,-0.29289806,female,cross,Insecta,between
2544,Sitobion avenae,343,rayyan-697472641,Genetic basis and selection for life-history trait plasticity on alternative host plants for the cereal aphid Sitobion avenae,2014,2013,"Qinghai, China",lab,female,female,NA,NA,6,6,NA,NA,NA,NA,NA,NA,animal_model,genetic_line,no,broad,authors,non_adult,non_adult,development time 3rd instar,development time 5th instar,reverse_maturation,reverse_maturation,include,cor,0.2999,NA,NA,NA,NA,NA,NA,NA,NA,Qinghai_oat,table 3,maturation,maturation,genotype,0.309409718,6,1,0.309409718,female,non_adult,Insecta,within
2545,Sitobion avenae,343,rayyan-697472641,Genetic basis and selection for life-history trait plasticity on alternative host plants for the cereal aphid Sitobion avenae,2014,2013,"Shaanxi, China",lab,female,female,NA,NA,10,10,NA,NA,NA,NA,NA,NA,animal_model,genetic_line,no,broad,authors,non_adult,non_adult,development time 1st instar,development time 5th instar,reverse_maturation,reverse_maturation,include,cor,0.3304,NA,NA,NA,NA,NA,NA,NA,NA,Shaanxi_oat,table 3,maturation,maturation,genotype,0.343277204,10,1,0.343277204,female,non_adult,Insecta,within
2546,Sitobion avenae,343,rayyan-697472641,Genetic basis and selection for life-history trait plasticity on alternative host plants for the cereal aphid Sitobion avenae,2014,2013,"Shaanxi, China",lab,female,female,NA,NA,10,10,NA,NA,NA,NA,NA,NA,animal_model,genetic_line,no,broad,authors,non_adult,adult,development time 1st instar,7 day fecundity,reverse_maturation,fertility,include,cor,-0.24555,NA,NA,NA,NA,NA,NA,NA,NA,Shaanxi_oat,table 3,maturation,fertility,genotype,-0.250671736,10,-1,0.250671736,female,cross,Insecta,between
2547,Sitobion avenae,343,rayyan-697472641,Genetic basis and selection for life-history trait plasticity on alternative host plants for the cereal aphid Sitobion avenae,2014,2013,"Qinghai, China",lab,female,female,NA,NA,6,6,NA,NA,NA,NA,NA,NA,animal_model,genetic_line,no,broad,authors,non_adult,adult,development time 4th instar,7 day fecundity,reverse_maturation,fertility,include,cor,0.4762,NA,NA,NA,NA,NA,NA,NA,NA,Qinghai_oat,table 3,maturation,fertility,genotype,0.518058283,6,-1,-0.518058283,female,cross,Insecta,between
2548,Sitobion avenae,343,rayyan-697472641,Genetic basis and selection for life-history trait plasticity on alternative host plants for the cereal aphid Sitobion avenae,2014,2013,"Qinghai, China",lab,female,female,NA,NA,6,6,NA,NA,NA,NA,NA,NA,animal_model,genetic_line,no,broad,authors,non_adult,non_adult,development time 1st instar,development time 2nd instar,reverse_maturation,reverse_maturation,include,cor,-0.9079,NA,NA,NA,NA,NA,NA,NA,NA,Qinghai_barley,table 3,maturation,maturation,genotype,-1.515441748,6,1,-1.515441748,female,non_adult,Insecta,within
2549,Sitobion avenae,343,rayyan-697472641,Genetic basis and selection for life-history trait plasticity on alternative host plants for the cereal aphid Sitobion avenae,2014,2013,"Shaanxi, China",lab,female,female,NA,NA,10,10,NA,NA,NA,NA,NA,NA,animal_model,genetic_line,no,broad,authors,non_adult,non_adult,development time 2nd instar,development time 5th instar,reverse_maturation,reverse_maturation,include,cor,0.3874,NA,NA,NA,NA,NA,NA,NA,NA,Shaanxi_oat,table 3,maturation,maturation,genotype,0.408737288,10,1,0.408737288,female,non_adult,Insecta,within
2550,Sitobion avenae,343,rayyan-697472641,Genetic basis and selection for life-history trait plasticity on alternative host plants for the cereal aphid Sitobion avenae,2014,2013,"Shaanxi, China",lab,female,female,NA,NA,10,10,NA,NA,NA,NA,NA,NA,animal_model,genetic_line,no,broad,authors,non_adult,adult,development time 2nd instar,7 day fecundity,reverse_maturation,fertility,include,cor,-0.0464,NA,NA,NA,NA,NA,NA,NA,NA,Shaanxi_oat,table 3,maturation,fertility,genotype,-0.046433342,10,-1,0.046433342,female,cross,Insecta,between
2551,Sitobion avenae,343,rayyan-697472641,Genetic basis and selection for life-history trait plasticity on alternative host plants for the cereal aphid Sitobion avenae,2014,2013,"Shaanxi, China",lab,female,female,NA,NA,10,10,NA,NA,NA,NA,NA,NA,animal_model,genetic_line,no,broad,authors,non_adult,non_adult,development time 3rd instar,development time 4th instar,reverse_maturation,reverse_maturation,include,cor,0.2259,NA,NA,NA,NA,NA,NA,NA,NA,Shaanxi_oat,table 3,maturation,maturation,genotype,0.229864741,10,1,0.229864741,female,non_adult,Insecta,within
2552,Sitobion avenae,343,rayyan-697472641,Genetic basis and selection for life-history trait plasticity on alternative host plants for the cereal aphid Sitobion avenae,2014,2013,"Qinghai, China",lab,female,female,NA,NA,6,6,NA,NA,NA,NA,NA,NA,animal_model,genetic_line,no,broad,authors,non_adult,non_adult,development time 1st instar,development time 5th instar,reverse_maturation,reverse_maturation,include,cor,0.1778,NA,NA,NA,NA,NA,NA,NA,NA,Qinghai_wheat,table 3,maturation,maturation,genotype,0.179709948,6,1,0.179709948,female,non_adult,Insecta,within
2553,Sitobion avenae,343,rayyan-697472641,Genetic basis and selection for life-history trait plasticity on alternative host plants for the cereal aphid Sitobion avenae,2014,2013,"Shaanxi, China",lab,female,female,NA,NA,10,10,NA,NA,NA,NA,NA,NA,animal_model,genetic_line,no,broad,authors,non_adult,adult,development time 3rd instar,7 day fecundity,reverse_maturation,fertility,include,cor,0.3048,NA,NA,NA,NA,NA,NA,NA,NA,Shaanxi_oat,table 3,maturation,fertility,genotype,0.314802739,10,-1,-0.314802739,female,cross,Insecta,between
2554,Sitobion avenae,343,rayyan-697472641,Genetic basis and selection for life-history trait plasticity on alternative host plants for the cereal aphid Sitobion avenae,2014,2013,"Shaanxi, China",lab,female,female,NA,NA,10,10,NA,NA,NA,NA,NA,NA,animal_model,genetic_line,no,broad,authors,non_adult,non_adult,development time 1st instar,development time 3rd instar,reverse_maturation,reverse_maturation,include,cor,0.172,NA,NA,NA,NA,NA,NA,NA,NA,Shaanxi_wheat,table 3,maturation,maturation,genotype,0.173726908,10,1,0.173726908,female,non_adult,Insecta,within
2555,Sitobion avenae,343,rayyan-697472641,Genetic basis and selection for life-history trait plasticity on alternative host plants for the cereal aphid Sitobion avenae,2014,2013,"Qinghai, China",lab,female,female,NA,NA,6,6,NA,NA,NA,NA,NA,NA,animal_model,genetic_line,no,broad,authors,non_adult,non_adult,development time 3rd instar,development time 5th instar,reverse_maturation,reverse_maturation,include,cor,0.0703,NA,NA,NA,NA,NA,NA,NA,NA,Qinghai_wheat,table 3,maturation,maturation,genotype,0.070416154,6,1,0.070416154,female,non_adult,Insecta,within
2556,Sitobion avenae,343,rayyan-697472641,Genetic basis and selection for life-history trait plasticity on alternative host plants for the cereal aphid Sitobion avenae,2014,2013,"Qinghai, China",lab,female,female,NA,NA,6,6,NA,NA,NA,NA,NA,NA,animal_model,genetic_line,no,broad,authors,non_adult,adult,development time 2nd instar,7 day fecundity,reverse_maturation,fertility,include,cor,0.0425,NA,NA,NA,NA,NA,NA,NA,NA,Qinghai_oat,table 3,maturation,fertility,genotype,0.042525616,6,-1,-0.042525616,female,cross,Insecta,between
2557,Sitobion avenae,343,rayyan-697472641,Genetic basis and selection for life-history trait plasticity on alternative host plants for the cereal aphid Sitobion avenae,2014,2013,"Shaanxi, China",lab,female,female,NA,NA,10,10,NA,NA,NA,NA,NA,NA,animal_model,genetic_line,no,broad,authors,non_adult,non_adult,development time 1st instar,development time 2nd instar,reverse_maturation,reverse_maturation,include,cor,0.3634,NA,NA,NA,NA,NA,NA,NA,NA,Shaanxi_wheat,table 3,maturation,maturation,genotype,0.380797672,10,1,0.380797672,female,non_adult,Insecta,within
2558,Sitobion avenae,343,rayyan-697472641,Genetic basis and selection for life-history trait plasticity on alternative host plants for the cereal aphid Sitobion avenae,2014,2013,"Qinghai, China",lab,female,female,NA,NA,6,6,NA,NA,NA,NA,NA,NA,animal_model,genetic_line,no,broad,authors,non_adult,non_adult,development time 1st instar,development time 3rd instar,reverse_maturation,reverse_maturation,include,cor,0.048,NA,NA,NA,NA,NA,NA,NA,NA,Qinghai_barley,table 3,maturation,maturation,genotype,0.048036915,6,1,0.048036915,female,non_adult,Insecta,within
2559,Sitobion avenae,343,rayyan-697472641,Genetic basis and selection for life-history trait plasticity on alternative host plants for the cereal aphid Sitobion avenae,2014,2013,"Qinghai, China",lab,female,female,NA,NA,6,6,NA,NA,NA,NA,NA,NA,animal_model,genetic_line,no,broad,authors,non_adult,non_adult,development time 1st instar,development time 4th instar,reverse_maturation,reverse_maturation,include,cor,0.5144,NA,NA,NA,NA,NA,NA,NA,NA,Qinghai_barley,table 3,maturation,maturation,genotype,0.56869468,6,1,0.56869468,female,non_adult,Insecta,within
2560,Sitobion avenae,343,rayyan-697472641,Genetic basis and selection for life-history trait plasticity on alternative host plants for the cereal aphid Sitobion avenae,2014,2013,"Qinghai, China",lab,female,female,NA,NA,6,6,NA,NA,NA,NA,NA,NA,animal_model,genetic_line,no,broad,authors,non_adult,adult,development time 3rd instar,7 day fecundity,reverse_maturation,fertility,include,cor,-0.3055,NA,NA,NA,NA,NA,NA,NA,NA,Qinghai_wheat,table 3,maturation,fertility,genotype,-0.315574613,6,-1,0.315574613,female,cross,Insecta,between
2561,Sitobion avenae,343,rayyan-697472641,Genetic basis and selection for life-history trait plasticity on alternative host plants for the cereal aphid Sitobion avenae,2014,2013,"Shaanxi, China",lab,female,female,NA,NA,10,10,NA,NA,NA,NA,NA,NA,animal_model,genetic_line,no,broad,authors,non_adult,non_adult,development time 2nd instar,development time 3rd instar,reverse_maturation,reverse_maturation,include,cor,-0.0943,NA,NA,NA,NA,NA,NA,NA,NA,Shaanxi_oat,table 3,maturation,maturation,genotype,-0.094581022,10,1,-0.094581022,female,non_adult,Insecta,within
2562,Sitobion avenae,343,rayyan-697472641,Genetic basis and selection for life-history trait plasticity on alternative host plants for the cereal aphid Sitobion avenae,2014,2013,"Shaanxi, China",lab,female,female,NA,NA,10,10,NA,NA,NA,NA,NA,NA,animal_model,genetic_line,no,broad,authors,non_adult,non_adult,development time 3rd instar,development time 5th instar,reverse_maturation,reverse_maturation,include,cor,0.1953,NA,NA,NA,NA,NA,NA,NA,NA,Shaanxi_oat,table 3,maturation,maturation,genotype,0.197841471,10,1,0.197841471,female,non_adult,Insecta,within
2563,Sitobion avenae,343,rayyan-697472641,Genetic basis and selection for life-history trait plasticity on alternative host plants for the cereal aphid Sitobion avenae,2014,2013,"Qinghai, China",lab,female,female,NA,NA,6,6,NA,NA,NA,NA,NA,NA,animal_model,genetic_line,no,broad,authors,non_adult,non_adult,development time 4th instar,development time 5th instar,reverse_maturation,reverse_maturation,include,cor,0.3724,NA,NA,NA,NA,NA,NA,NA,NA,Qinghai_barley,table 3,maturation,maturation,genotype,0.391206645,6,1,0.391206645,female,non_adult,Insecta,within
2564,Sitobion avenae,343,rayyan-697472641,Genetic basis and selection for life-history trait plasticity on alternative host plants for the cereal aphid Sitobion avenae,2014,2013,"Shaanxi, China",lab,female,female,NA,NA,10,10,NA,NA,NA,NA,NA,NA,animal_model,genetic_line,no,broad,authors,non_adult,non_adult,development time 2nd instar,development time 5th instar,reverse_maturation,reverse_maturation,include,cor,-0.0046,NA,NA,NA,NA,NA,NA,NA,NA,Shaanxi_wheat,table 3,maturation,maturation,genotype,-0.004600032,10,1,-0.004600032,female,non_adult,Insecta,within
2565,Sitobion avenae,343,rayyan-697472641,Genetic basis and selection for life-history trait plasticity on alternative host plants for the cereal aphid Sitobion avenae,2014,2013,"Shaanxi, China",lab,female,female,NA,NA,10,10,NA,NA,NA,NA,NA,NA,animal_model,genetic_line,no,broad,authors,non_adult,non_adult,development time 4th instar,development time 5th instar,reverse_maturation,reverse_maturation,include,cor,0.5573,NA,NA,NA,NA,NA,NA,NA,NA,Shaanxi_oat,table 3,maturation,maturation,genotype,0.628908246,10,1,0.628908246,female,non_adult,Insecta,within
2566,Sitobion avenae,343,rayyan-697472641,Genetic basis and selection for life-history trait plasticity on alternative host plants for the cereal aphid Sitobion avenae,2014,2013,"Qinghai, China",lab,female,female,NA,NA,6,6,NA,NA,NA,NA,NA,NA,animal_model,genetic_line,no,broad,authors,non_adult,non_adult,development time 3rd instar,development time 4th instar,reverse_maturation,reverse_maturation,include,cor,0.1041,NA,NA,NA,NA,NA,NA,NA,NA,Qinghai_oat,table 3,maturation,maturation,genotype,0.104478501,6,1,0.104478501,female,non_adult,Insecta,within
2567,Sitobion avenae,343,rayyan-697472641,Genetic basis and selection for life-history trait plasticity on alternative host plants for the cereal aphid Sitobion avenae,2014,2013,"Shaanxi, China",lab,female,female,NA,NA,10,10,NA,NA,NA,NA,NA,NA,animal_model,genetic_line,no,broad,authors,non_adult,adult,development time 1st instar,7 day fecundity,reverse_maturation,fertility,include,cor,-0.0846,NA,NA,NA,NA,NA,NA,NA,NA,Shaanxi_wheat,table 3,maturation,fertility,genotype,-0.084802703,10,-1,0.084802703,female,cross,Insecta,between
2568,Sitobion avenae,343,rayyan-697472641,Genetic basis and selection for life-history trait plasticity on alternative host plants for the cereal aphid Sitobion avenae,2014,2013,"Shaanxi, China",lab,female,female,NA,NA,10,10,NA,NA,NA,NA,NA,NA,animal_model,genetic_line,no,broad,authors,non_adult,non_adult,development time 2nd instar,development time 3rd instar,reverse_maturation,reverse_maturation,include,cor,0.1964,NA,NA,NA,NA,NA,NA,NA,NA,Shaanxi_barley,table 3,maturation,maturation,genotype,0.198985347,10,1,0.198985347,female,non_adult,Insecta,within
2569,Sitobion avenae,343,rayyan-697472641,Genetic basis and selection for life-history trait plasticity on alternative host plants for the cereal aphid Sitobion avenae,2014,2013,"Shaanxi, China",lab,female,female,NA,NA,10,10,NA,NA,NA,NA,NA,NA,animal_model,genetic_line,no,broad,authors,non_adult,non_adult,development time 1st instar,development time 4th instar,reverse_maturation,reverse_maturation,include,cor,0.2832,NA,NA,NA,NA,NA,NA,NA,NA,Shaanxi_wheat,table 3,maturation,maturation,genotype,0.291157688,10,1,0.291157688,female,non_adult,Insecta,within
2570,Sitobion avenae,343,rayyan-697472641,Genetic basis and selection for life-history trait plasticity on alternative host plants for the cereal aphid Sitobion avenae,2014,2013,"Shaanxi, China",lab,female,female,NA,NA,10,10,NA,NA,NA,NA,NA,NA,animal_model,genetic_line,no,broad,authors,non_adult,non_adult,development time 1st instar,development time 5th instar,reverse_maturation,reverse_maturation,include,cor,0.1812,NA,NA,NA,NA,NA,NA,NA,NA,Shaanxi_wheat,table 3,maturation,maturation,genotype,0.183223148,10,1,0.183223148,female,non_adult,Insecta,within
2571,Sitobion avenae,343,rayyan-697472641,Genetic basis and selection for life-history trait plasticity on alternative host plants for the cereal aphid Sitobion avenae,2014,2013,"Shaanxi, China",lab,female,female,NA,NA,10,10,NA,NA,NA,NA,NA,NA,animal_model,genetic_line,no,broad,authors,non_adult,adult,development time 4th instar,7 day fecundity,reverse_maturation,fertility,include,cor,0.2568,NA,NA,NA,NA,NA,NA,NA,NA,Shaanxi_oat,table 3,maturation,fertility,genotype,0.26267945,10,-1,-0.26267945,female,cross,Insecta,between
2572,Sitobion avenae,343,rayyan-697472641,Genetic basis and selection for life-history trait plasticity on alternative host plants for the cereal aphid Sitobion avenae,2014,2013,"Shaanxi, China",lab,female,female,NA,NA,10,10,NA,NA,NA,NA,NA,NA,animal_model,genetic_line,no,broad,authors,non_adult,non_adult,development time 2nd instar,development time 3rd instar,reverse_maturation,reverse_maturation,include,cor,0.0999,NA,NA,NA,NA,NA,NA,NA,NA,Shaanxi_wheat,table 3,maturation,maturation,genotype,0.100234339,10,1,0.100234339,female,non_adult,Insecta,within
2573,Sitobion avenae,343,rayyan-697472641,Genetic basis and selection for life-history trait plasticity on alternative host plants for the cereal aphid Sitobion avenae,2014,2013,"Shaanxi, China",lab,female,female,NA,NA,10,10,NA,NA,NA,NA,NA,NA,animal_model,genetic_line,no,broad,authors,non_adult,non_adult,development time 2nd instar,development time 4th instar,reverse_maturation,reverse_maturation,include,cor,0.3825,NA,NA,NA,NA,NA,NA,NA,NA,Shaanxi_wheat,table 3,maturation,maturation,genotype,0.402984832,10,1,0.402984832,female,non_adult,Insecta,within
2574,Sitobion avenae,343,rayyan-697472641,Genetic basis and selection for life-history trait plasticity on alternative host plants for the cereal aphid Sitobion avenae,2014,2013,"Shaanxi, China",lab,female,female,NA,NA,10,10,NA,NA,NA,NA,NA,NA,animal_model,genetic_line,no,broad,authors,non_adult,non_adult,development time 1st instar,development time 4th instar,reverse_maturation,reverse_maturation,include,cor,0.0602,NA,NA,NA,NA,NA,NA,NA,NA,Shaanxi_oat,table 3,maturation,maturation,genotype,0.060272881,10,1,0.060272881,female,non_adult,Insecta,within
2575,Sitobion avenae,343,rayyan-697472641,Genetic basis and selection for life-history trait plasticity on alternative host plants for the cereal aphid Sitobion avenae,2014,2013,"Shaanxi, China",lab,female,female,NA,NA,10,10,NA,NA,NA,NA,NA,NA,animal_model,genetic_line,no,broad,authors,non_adult,non_adult,development time 1st instar,development time 3rd instar,reverse_maturation,reverse_maturation,include,cor,-0.2651,NA,NA,NA,NA,NA,NA,NA,NA,Shaanxi_oat,table 3,maturation,maturation,genotype,-0.271586007,10,1,-0.271586007,female,non_adult,Insecta,within
2576,Stator limbatus,108,rayyan-697471799,Evolutionary ecology of egg size and number in a seed beetle: Genetic trade-off differs between environments,2003,1998,"Pinal County, Arizona",lab,female,female,600,600,1,1,600,600,600,600,1800,1800,correlated_selection,half_sib,yes,narrow,authors,adult,non_adult,adult body mass,egg length,size,size,include,cor,0.23,NA,NA,NA,NA,NA,NA,NA,NA,realized_up_selection_Cercidium_rep1,table 4,size,size,family,0.234189467,600,1,0.234189467,female,cross,Insecta,within
2577,Stator limbatus,108,rayyan-697471799,Evolutionary ecology of egg size and number in a seed beetle: Genetic trade-off differs between environments,2003,1998,"Pinal County, Arizona",lab,female,female,600,600,1,1,600,600,600,600,1800,1800,correlated_selection,half_sib,yes,narrow,authors,adult,non_adult,adult body mass,egg length,size,size,include,cor,0.21,NA,NA,NA,NA,NA,NA,NA,NA,realized_up_selection_Acadia_rep1,table 4,size,size,family,0.213171347,600,1,0.213171347,female,cross,Insecta,within
2578,Stator limbatus,108,rayyan-697471799,Evolutionary ecology of egg size and number in a seed beetle: Genetic trade-off differs between environments,2003,1998,"Pinal County, Arizona",lab,female,female,600,600,1,1,600,600,600,600,1800,1800,correlated_selection,half_sib,yes,narrow,authors,adult,non_adult,adult body mass,egg length,size,size,include,cor,0.27,NA,NA,NA,NA,NA,NA,NA,NA,realized_up_selection_Acadia_rep2,table 4,size,size,family,0.276863823,600,1,0.276863823,female,cross,Insecta,within
2579,Stator limbatus,108,rayyan-697471799,Evolutionary ecology of egg size and number in a seed beetle: Genetic trade-off differs between environments,2003,1998,"Pinal County, Arizona",lab,female,female,600,600,1,1,600,600,600,600,1800,1800,correlated_selection,half_sib,yes,narrow,authors,adult,non_adult,adult body mass,egg length,size,size,include,cor,0.24,NA,NA,NA,NA,NA,NA,NA,NA,realized_up_selection_Acadia_rep1,table 4,size,size,family,0.244774113,600,1,0.244774113,female,cross,Insecta,within
2580,Stator limbatus,108,rayyan-697471799,Evolutionary ecology of egg size and number in a seed beetle: Genetic trade-off differs between environments,2003,1998,"Pinal County, Arizona",lab,female,female,404,404,NA,NA,511,511,126,126,2797,2667,animal_model,half_sib,no,narrow,authors,adult,adult,adult body mass,fecundity,size,fertility,include,cor,0.44,0.3,se,NA,NA,NA,NA,NA,NA,estimated_Cercidium_half_sib,table 4,size,fertility,family,0.472230804,404,1,0.472230804,female,adult,Insecta,between
2581,Stator limbatus,108,rayyan-697471799,Evolutionary ecology of egg size and number in a seed beetle: Genetic trade-off differs between environments,2003,1998,"Pinal County, Arizona",lab,female,female,600,600,1,1,600,600,600,600,1800,1800,correlated_selection,half_sib,yes,narrow,authors,adult,non_adult,adult body mass,egg length,size,size,include,cor,0.05,NA,NA,NA,NA,NA,NA,NA,NA,realized_up_selection_Cercidium_rep2,table 4,size,size,family,0.050041729,600,1,0.050041729,female,cross,Insecta,within
2582,Stator limbatus,108,rayyan-697471799,Evolutionary ecology of egg size and number in a seed beetle: Genetic trade-off differs between environments,2003,1998,"Pinal County, Arizona",lab,female,female,404,404,NA,NA,511,511,126,126,2797,2667,animal_model,half_sib,no,narrow,authors,adult,non_adult,adult body mass,egg length,size,size,include,cor,-0.07,0.25,se,NA,NA,NA,NA,NA,NA,estimated_Cercidium_half_sib,table 4,size,size,family,-0.070114671,404,1,-0.070114671,female,cross,Insecta,within
2583,Stator limbatus,108,rayyan-697471799,Evolutionary ecology of egg size and number in a seed beetle: Genetic trade-off differs between environments,2003,1998,"Pinal County, Arizona",lab,female,female,600,600,1,1,600,600,600,600,1800,1800,correlated_selection,half_sib,yes,narrow,authors,non_adult,adult,egg length,fecundity,size,fertility,include,cor,-0.44,NA,NA,NA,NA,NA,NA,NA,NA,realized_up_selection_Cercidium_rep2,table 6,size,fertility,family,-0.472230804,600,1,-0.472230804,female,cross,Insecta,between
2584,Stator limbatus,108,rayyan-697471799,Evolutionary ecology of egg size and number in a seed beetle: Genetic trade-off differs between environments,2003,1998,"Pinal County, Arizona",lab,female,female,600,600,1,1,600,600,600,600,1800,1800,correlated_selection,half_sib,yes,narrow,authors,non_adult,adult,egg length,fecundity,size,fertility,include,cor,-0.28,NA,NA,NA,NA,NA,NA,NA,NA,realized_up_selection_Cercidium_rep1,table 6,size,fertility,family,-0.287682072,600,1,-0.287682072,female,cross,Insecta,between
2585,Stator limbatus,108,rayyan-697471799,Evolutionary ecology of egg size and number in a seed beetle: Genetic trade-off differs between environments,2003,1998,"Pinal County, Arizona",lab,female,female,404,404,NA,NA,511,511,126,126,2797,2667,animal_model,half_sib,no,narrow,authors,adult,adult,adult body mass,fecundity,size,fertility,include,cor,0.28,0.32,se,NA,NA,NA,NA,NA,NA,estimated_Aracia_half_sib,table 4,size,fertility,family,0.287682072,404,1,0.287682072,female,adult,Insecta,between
2586,Stator limbatus,108,rayyan-697471799,Evolutionary ecology of egg size and number in a seed beetle: Genetic trade-off differs between environments,2003,1998,"Pinal County, Arizona",lab,female,female,600,600,1,1,600,600,600,600,1800,1800,correlated_selection,half_sib,yes,narrow,authors,adult,non_adult,adult body mass,egg length,size,size,include,cor,-0.08,NA,NA,NA,NA,NA,NA,NA,NA,realized_up_selection_Cercidium_rep1,table 4,size,size,family,-0.080171325,600,1,-0.080171325,female,cross,Insecta,within
2587,Stator limbatus,108,rayyan-697471799,Evolutionary ecology of egg size and number in a seed beetle: Genetic trade-off differs between environments,2003,1998,"Pinal County, Arizona",lab,female,female,600,600,1,1,600,600,600,600,1800,1800,correlated_selection,half_sib,yes,narrow,authors,non_adult,adult,egg length,fecundity,size,fertility,include,cor,0.04,NA,NA,NA,NA,NA,NA,NA,NA,realized_up_selection_Acadia_rep2,table 6,size,fertility,family,0.040021354,600,1,0.040021354,female,cross,Insecta,between
2588,Stator limbatus,108,rayyan-697471799,Evolutionary ecology of egg size and number in a seed beetle: Genetic trade-off differs between environments,2003,1998,"Pinal County, Arizona",lab,female,female,600,600,1,1,600,600,600,600,1800,1800,correlated_selection,half_sib,yes,narrow,authors,non_adult,adult,egg length,fecundity,size,fertility,include,cor,-0.09,NA,NA,NA,NA,NA,NA,NA,NA,realized_up_selection_Acadia_rep1,table 6,size,fertility,family,-0.090244188,600,1,-0.090244188,female,cross,Insecta,between
2589,Stator limbatus,108,rayyan-697471799,Evolutionary ecology of egg size and number in a seed beetle: Genetic trade-off differs between environments,2003,1998,"Pinal County, Arizona",lab,female,female,600,600,1,1,600,600,600,600,1800,1800,correlated_selection,half_sib,yes,narrow,authors,non_adult,adult,egg length,fecundity,size,fertility,include,cor,-0.09,NA,NA,NA,NA,NA,NA,NA,NA,realized_up_selection_Acadia_rep2,table 6,size,fertility,family,-0.090244188,600,1,-0.090244188,female,cross,Insecta,between
2590,Stator limbatus,108,rayyan-697471799,Evolutionary ecology of egg size and number in a seed beetle: Genetic trade-off differs between environments,2003,1998,"Pinal County, Arizona",lab,female,female,404,404,NA,NA,511,511,126,126,2797,2667,animal_model,half_sib,no,narrow,authors,adult,non_adult,adult body mass,egg length,size,size,include,cor,0.32,0.19,se,NA,NA,NA,NA,NA,NA,estimated_Aracia_half_sib,table 4,size,size,family,0.331647109,404,1,0.331647109,female,cross,Insecta,within
2591,Stator limbatus,108,rayyan-697471799,Evolutionary ecology of egg size and number in a seed beetle: Genetic trade-off differs between environments,2003,1998,"Pinal County, Arizona",lab,female,female,404,404,NA,NA,511,511,126,126,2667,2667,animal_model,half_sib,no,narrow,authors,both,adult,residual of egg length over female body mass,residual of fecundity over female body mass,size,fertility,include,cor,-0.25,0.18,se,NA,NA,NA,NA,NA,NA,estimated_Aracia_half_sib,table 6,size,fertility,family,-0.255412812,404,1,-0.255412812,female,cross,Insecta,between
2592,Stator limbatus,108,rayyan-697471799,Evolutionary ecology of egg size and number in a seed beetle: Genetic trade-off differs between environments,2003,1998,"Pinal County, Arizona",lab,female,female,404,404,NA,NA,511,511,126,126,2667,2667,animal_model,half_sib,no,narrow,authors,both,adult,residual of egg length over female body mass,residual of fecundity over female body mass,size,fertility,include,cor,-0.55,0.15,se,NA,NA,NA,NA,NA,NA,estimated_Cercidium_half_sib,table 6,size,fertility,family,-0.618381314,404,1,-0.618381314,female,cross,Insecta,between
2593,Stator limbatus,108,rayyan-697471799,Evolutionary ecology of egg size and number in a seed beetle: Genetic trade-off differs between environments,2003,1998,"Pinal County, Arizona",lab,female,female,600,600,1,1,600,600,600,600,1800,1800,correlated_selection,half_sib,yes,narrow,authors,non_adult,adult,egg length,fecundity,size,fertility,include,cor,-0.4,NA,NA,NA,NA,NA,NA,NA,NA,realized_up_selection_Cercidium_rep1,table 6,size,fertility,family,-0.42364893,600,1,-0.42364893,female,cross,Insecta,between
2594,Stator limbatus,108,rayyan-697471799,Evolutionary ecology of egg size and number in a seed beetle: Genetic trade-off differs between environments,2003,1998,"Pinal County, Arizona",lab,female,female,600,600,1,1,600,600,600,600,1800,1800,correlated_selection,half_sib,yes,narrow,authors,adult,non_adult,adult body mass,egg length,size,size,include,cor,0.17,NA,NA,NA,NA,NA,NA,NA,NA,realized_up_selection_Acadia_rep2,table 4,size,size,family,0.171666664,600,1,0.171666664,female,cross,Insecta,within
2595,Stator limbatus,108,rayyan-697471799,Evolutionary ecology of egg size and number in a seed beetle: Genetic trade-off differs between environments,2003,1998,"Pinal County, Arizona",lab,female,female,600,600,1,1,600,600,600,600,1800,1800,correlated_selection,half_sib,yes,narrow,authors,non_adult,adult,egg length,fecundity,size,fertility,include,cor,-0.03,NA,NA,NA,NA,NA,NA,NA,NA,realized_up_selection_Acadia_rep1,table 6,size,fertility,family,-0.030009005,600,1,-0.030009005,female,cross,Insecta,between
2596,Stator limbatus,108,rayyan-697471799,Evolutionary ecology of egg size and number in a seed beetle: Genetic trade-off differs between environments,2003,1998,"Pinal County, Arizona",lab,female,female,404,404,NA,NA,511,511,126,126,2667,2667,animal_model,half_sib,no,narrow,authors,non_adult,adult,egg length,fecundity,size,fertility,include,cor,-0.13,0.21,se,NA,NA,NA,NA,NA,NA,estimated_Aracia_half_sib,table 6,size,fertility,family,-0.13073985,404,1,-0.13073985,female,cross,Insecta,between
2597,Stator limbatus,108,rayyan-697471799,Evolutionary ecology of egg size and number in a seed beetle: Genetic trade-off differs between environments,2003,1998,"Pinal County, Arizona",lab,female,female,404,404,NA,NA,511,511,126,126,2667,2667,animal_model,half_sib,no,narrow,authors,non_adult,adult,egg length,fecundity,size,fertility,include,cor,-0.51,0.18,se,NA,NA,NA,NA,NA,NA,estimated_Cercidium_half_sib,table 6,size,fertility,family,-0.562729769,404,1,-0.562729769,female,cross,Insecta,between
2598,Stator limbatus,108,rayyan-697471799,Evolutionary ecology of egg size and number in a seed beetle: Genetic trade-off differs between environments,2003,1998,"Pinal County, Arizona",lab,female,female,600,600,1,1,600,600,600,600,1800,1800,correlated_selection,half_sib,yes,narrow,authors,adult,non_adult,adult body mass,egg length,size,size,include,cor,-0.15,NA,NA,NA,NA,NA,NA,NA,NA,realized_up_selection_Cercidium_rep2,table 4,size,size,family,-0.151140436,600,1,-0.151140436,female,cross,Insecta,within
2599,Stator limbatus,108,rayyan-697471799,Evolutionary ecology of egg size and number in a seed beetle: Genetic trade-off differs between environments,2003,1998,"Pinal County, Arizona",lab,female,female,600,600,1,1,600,600,600,600,1800,1800,correlated_selection,half_sib,yes,narrow,authors,non_adult,adult,egg length,fecundity,size,fertility,include,cor,-0.4,NA,NA,NA,NA,NA,NA,NA,NA,realized_up_selection_Cercidium_rep2,table 6,size,fertility,family,-0.42364893,600,1,-0.42364893,female,cross,Insecta,between
2607,Tetranychus kanzawai,84,rayyan-697471715,Negative genetic correlation between diapause duration and fecundity after diapause in a spider mite,2007,2000,"Kyoto, Japan",lab,female,female,145,145,NA,NA,145,145,29,29,435,435,animal_model,half_sib,no,narrow,authors,adult,adult,total fecundity,early fecundity (first 9 days),fertility,fertility,include_2,cor,0.98,"[0.77, 1.19]",95CI,NA,NA,NA,NA,NA,NA,half-sib_jacknife,table 2,fertility,fertility,family,2.297559925,145,1,2.297559925,female,adult,Arachnida,within
2608,Tetranychus urticae,75,rayyan-697471660,Heritability of defence and life-history traits in the two-spotted spider mite,2009,2005,"Castricum, Netherland",lab,female,female,55,48,NA,NA,55,48,NA,NA,110,96,parent_offspring_regression,parent_offspring_pair,no,broad,CC,adult,adult,oviposition rate (number of eggs produced in the same period),number of offspring,fertility,fertility,include_2,cor,0.9,NA,NA,NA,NA,NA,NA,NA,NA,daughter_correlated_with_mother,table 2,fertility,fertility,family,1.47221949,48,1,1.47221949,female,adult,Arachnida,within
2610,Tetranychus urticae,75,rayyan-697471660,Heritability of defence and life-history traits in the two-spotted spider mite,2009,2005,"Castricum, Netherland",lab,female,female,55,48,NA,NA,55,48,NA,NA,110,96,parent_offspring_regression,parent_offspring_pair,no,broad,CC,adult,adult,oviposition rate (number of eggs produced in the same period),number of daughters,fertility,fertility,include_2,cor,0.2,NA,NA,NA,NA,NA,NA,NA,NA,daughter_correlated_with_mother,table 2,fertility,fertility,family,0.202732554,48,1,0.202732554,female,adult,Arachnida,within
2611,Tetranychus urticae,75,rayyan-697471660,Heritability of defence and life-history traits in the two-spotted spider mite,2009,2005,"Castricum, Netherland",lab,female,female,48,48,NA,NA,48,48,NA,NA,96,96,parent_offspring_regression,parent_offspring_pair,no,broad,CC,adult,adult,number of daughters,number of offspring,fertility,fertility,include_2,cor,0.27,NA,NA,NA,NA,NA,NA,NA,NA,daughter_correlated_with_mother,table 2,fertility,fertility,family,0.276863823,48,1,0.276863823,female,adult,Arachnida,within
2614,Tetrix undulata,104,rayyan-697471791,"Correlated evolution of colour pattern and body size in polymorphic pygmy grasshoppers, Tetrix undulata",2003,2000,"50 km south of Växjö, south central Sweden",lab,both,both,75,75,NA,NA,75,75,75,75,NA,NA,family_mean_correlation,full_sib,no,broad,authors,adult,both,number of hatchling released,proportion of individuals that survived the adult stage at the time of the first census,fertility,survival,include,cor,-0.13,NA,NA,NA,NA,NA,NA,NA,NA,warm,2nd para of general information,fertility,survival,family,-0.13073985,75,1,-0.13073985,both,cross,Insecta,between
2615,Tetrix undulata,104,rayyan-697471791,"Correlated evolution of colour pattern and body size in polymorphic pygmy grasshoppers, Tetrix undulata",2003,2000,"57 km south of Växjö, south central Sweden",lab,both,both,48,48,NA,NA,48,48,48,48,NA,NA,family_mean_correlation,full_sib,no,broad,authors,adult,non_adult,body size of mature offspring,proportion of individuals that had reached the adult stage at the time of the first census,size,maturation,include,cor,0.48,NA,NA,NA,NA,NA,NA,NA,NA,cold,Association of time to maturity and adult body size,size,maturation,family,0.522984278,48,1,0.522984278,both,cross,Insecta,between
2616,Tetrix undulata,104,rayyan-697471791,"Correlated evolution of colour pattern and body size in polymorphic pygmy grasshoppers, Tetrix undulata",2003,2000,"53 km south of Växjö, south central Sweden",lab,both,both,69,69,NA,NA,69,69,69,69,NA,NA,family_mean_correlation,full_sib,no,broad,authors,adult,non_adult,number of hatchling released,proportion of individuals that had reached the adult stage at the time of the first census,fertility,maturation,include,cor,-0.05,NA,NA,NA,NA,NA,NA,NA,NA,cold,2nd para of general information,fertility,maturation,family,-0.050041729,69,1,-0.050041729,both,cross,Insecta,between
2617,Tetrix undulata,104,rayyan-697471791,"Correlated evolution of colour pattern and body size in polymorphic pygmy grasshoppers, Tetrix undulata",2003,2000,"51 km south of Växjö, south central Sweden",lab,both,both,75,75,NA,NA,75,75,75,75,NA,NA,family_mean_correlation,full_sib,no,broad,authors,adult,both,number of hatchling released,proportion of individuals that survived the adult stage at the time of the first census,fertility,survival,include,cor,0.74,NA,NA,NA,NA,NA,NA,NA,NA,cold,2nd para of general information,fertility,survival,family,0.950479381,75,1,0.950479381,both,cross,Insecta,between
2618,Tetrix undulata,104,rayyan-697471791,"Correlated evolution of colour pattern and body size in polymorphic pygmy grasshoppers, Tetrix undulata",2003,2000,"52 km south of Växjö, south central Sweden",lab,both,both,69,69,NA,NA,69,69,69,69,NA,NA,family_mean_correlation,full_sib,no,broad,authors,adult,non_adult,number of hatchling released,proportion of individuals that had reached the adult stage at the time of the first census,fertility,maturation,include,cor,-0.04,NA,NA,NA,NA,NA,NA,NA,NA,warm,2nd para of general information,fertility,maturation,family,-0.040021354,69,1,-0.040021354,both,cross,Insecta,between
2619,Tetrix undulata,104,rayyan-697471791,"Correlated evolution of colour pattern and body size in polymorphic pygmy grasshoppers, Tetrix undulata",2003,2000,"56 km south of Växjö, south central Sweden",lab,both,both,60,60,NA,NA,60,60,60,60,NA,NA,family_mean_correlation,full_sib,no,broad,authors,adult,non_adult,body size of mature offspring,proportion of individuals that had reached the adult stage at the time of the first census,size,maturation,include,cor,0.39,NA,NA,NA,NA,NA,NA,NA,NA,warm,Association of time to maturity and adult body size,size,maturation,family,0.411800034,60,1,0.411800034,both,cross,Insecta,between
2620,Tetrix undulata,104,rayyan-697471791,"Correlated evolution of colour pattern and body size in polymorphic pygmy grasshoppers, Tetrix undulata",2003,2000,"55 km south of Växjö, south central Sweden",lab,both,both,64,64,NA,NA,64,64,64,64,NA,NA,family_mean_correlation,full_sib,no,broad,authors,adult,adult,number of hatchling released,average adult body size,fertility,size,include,cor,-0.21,NA,NA,NA,NA,NA,NA,NA,NA,cold,2nd para of general information,fertility,size,family,-0.213171347,64,1,-0.213171347,both,adult,Insecta,between
2621,Tetrix undulata,104,rayyan-697471791,"Correlated evolution of colour pattern and body size in polymorphic pygmy grasshoppers, Tetrix undulata",2003,2000,"54 km south of Växjö, south central Sweden",lab,both,both,69,69,NA,NA,69,69,69,69,NA,NA,family_mean_correlation,full_sib,no,broad,authors,adult,adult,number of hatchling released,average adult body size,fertility,size,include,cor,-0.05,NA,NA,NA,NA,NA,NA,NA,NA,warm,2nd para of general information,fertility,size,family,-0.050041729,69,1,-0.050041729,both,adult,Insecta,between
2622,Tribolium castaneum,407,rayyan-697473064,Genetic variance in fitness and its cross-sex covariance predict adaptation during experimental evolution,2020,2010,NA,lab,female,female,NA,NA,NA,NA,441,441,147,147,1005,837,animal_model,half_sib,no,narrow,authors,adult,adult,fitness (number of adult offspring),size,fertility,size,include,cor,-0.18,0.348,se,NA,NA,NA,NA,NA,NA,female_hot,table s4,fertility,size,family,-0.181982689,441,1,-0.181982689,female,adult,Insecta,between
2623,Tribolium castaneum,407,rayyan-697473064,Genetic variance in fitness and its cross-sex covariance predict adaptation during experimental evolution,2020,2010,NA,lab,female,female,NA,NA,NA,NA,441,441,147,147,1396,960,animal_model,half_sib,no,narrow,authors,adult,adult,fitness (number of adult offspring),size,fertility,size,include,cor,0.06,0.214,se,NA,NA,NA,NA,NA,NA,female_hot_dry,table s4,fertility,size,family,0.060072156,441,1,0.060072156,female,adult,Insecta,between
2624,Tribolium castaneum,407,rayyan-697473064,Genetic variance in fitness and its cross-sex covariance predict adaptation during experimental evolution,2020,2010,NA,lab,female,female,NA,NA,NA,NA,441,441,147,147,1603,1181,animal_model,half_sib,no,narrow,authors,adult,adult,fitness (number of adult offspring),size,fertility,size,include,cor,0.013,0.26,se,NA,NA,NA,NA,NA,NA,female_dry,table s4,fertility,size,family,0.013000732,441,1,0.013000732,female,adult,Insecta,between
2625,Tribolium castaneum,407,rayyan-697473064,Genetic variance in fitness and its cross-sex covariance predict adaptation during experimental evolution,2020,2010,NA,lab,male,male,NA,NA,NA,NA,441,441,147,147,801.5,1183,animal_model,half_sib,no,narrow,authors,adult,adult,fitness (number of adult offspring),size,fertility,size,include,cor,0.216,0.24,se,NA,NA,NA,NA,NA,NA,male_dry,table s4,fertility,size,family,0.219456521,441,1,0.219456521,male,adult,Insecta,between
2626,Tribolium castaneum,407,rayyan-697473064,Genetic variance in fitness and its cross-sex covariance predict adaptation during experimental evolution,2020,2010,NA,lab,male,male,NA,NA,NA,NA,441,441,147,147,502.5,843,animal_model,half_sib,no,narrow,authors,adult,adult,fitness (number of adult offspring),size,fertility,size,include,cor,-0.177,0.285,se,NA,NA,NA,NA,NA,NA,male_hot,table s4,fertility,size,family,-0.178883953,441,1,-0.178883953,male,adult,Insecta,between
2627,Tribolium castaneum,407,rayyan-697473064,Genetic variance in fitness and its cross-sex covariance predict adaptation during experimental evolution,2020,2010,NA,lab,male,male,NA,NA,NA,NA,441,441,147,147,757,1008,animal_model,half_sib,no,narrow,authors,adult,adult,fitness (number of adult offspring),size,fertility,size,include,cor,-0.538,0.276,se,NA,NA,NA,NA,NA,NA,male_control,table s4,fertility,size,family,-0.601336629,441,1,-0.601336629,male,adult,Insecta,between
2628,Tribolium castaneum,407,rayyan-697473064,Genetic variance in fitness and its cross-sex covariance predict adaptation during experimental evolution,2020,2010,NA,lab,female,female,NA,NA,NA,NA,441,441,147,147,1514,1020,animal_model,half_sib,no,narrow,authors,adult,adult,fitness (number of adult offspring),size,fertility,size,include,cor,-0.256,0.29,se,NA,NA,NA,NA,NA,NA,female_control,table s4,fertility,size,family,-0.261823156,441,1,-0.261823156,female,adult,Insecta,between
2629,Tribolium castaneum,407,rayyan-697473064,Genetic variance in fitness and its cross-sex covariance predict adaptation during experimental evolution,2020,2010,NA,lab,male,male,NA,NA,NA,NA,441,441,147,147,698,962,animal_model,half_sib,no,narrow,authors,adult,adult,fitness (number of adult offspring),size,fertility,size,include,cor,0.299,0.207,se,NA,NA,NA,NA,NA,NA,male_hot_dry,table s4,fertility,size,family,0.308421065,441,1,0.308421065,male,adult,Insecta,between
2630,Trichogramma minutum,7,rayyan-178530584,Measurement and selection of parasitoid quality for mass-reared Trichogramma minutum riley used in inundative release,2000,1988-1992,"Ontario, Canada",lab,female,female,660,660,33,33,660,660,660,660,NA,NA,line_mean_correlation,genetic_line,yes,broad,authors,both,adult,female longevity,number of female offspring,survival,fertility,include,cor,0.281,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-178530584,table 3 fitness component,survival,fertility,genotype,0.288767472,33,1,0.288767472,female,cross,Insecta,between
2631,Trichogramma minutum,7,rayyan-178530584,Measurement and selection of parasitoid quality for mass-reared Trichogramma minutum riley used in inundative release,2000,1988-1992,"Ontario, Canada",lab,female,female,660,660,33,33,660,660,660,660,NA,NA,line_mean_correlation,genetic_line,yes,broad,authors,both,adult,female longevity,number of male offspring,survival,fertility,include,cor,0.328,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-178530584,table 3 fitness component,survival,fertility,genotype,0.340585495,33,1,0.340585495,female,cross,Insecta,between
2632,Trichogramma minutum,7,rayyan-178530584,Measurement and selection of parasitoid quality for mass-reared Trichogramma minutum riley used in inundative release,2000,1988-1992,"Ontario, Canada",lab,female,female,660,660,33,33,660,660,660,660,NA,NA,line_mean_correlation,genetic_line,yes,broad,authors,both,adult,female longevity,number of parasitized host eggs per female,survival,fertility,include,cor,0.333,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-178530584,table 3 fitness component,survival,fertility,genotype,0.346198637,33,1,0.346198637,female,cross,Insecta,between
2633,Trichogramma minutum,7,rayyan-178530584,Measurement and selection of parasitoid quality for mass-reared Trichogramma minutum riley used in inundative release,2000,1988-1992,"Ontario, Canada",lab,female,female,660,660,33,33,660,660,660,660,NA,NA,line_mean_correlation,genetic_line,yes,broad,authors,both,non_adult,female longevity,emergence of offspring (adult percentage),survival,survival,include,cor,0,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-178530584,table 3 fitness component,survival,survival,genotype,0,33,1,0,female,cross,Insecta,within
2634,Trichogramma minutum,7,rayyan-178530584,Measurement and selection of parasitoid quality for mass-reared Trichogramma minutum riley used in inundative release,2000,1988-1992,"Ontario, Canada",lab,female,female,660,660,33,33,660,660,660,660,NA,NA,line_mean_correlation,genetic_line,yes,broad,authors,non_adult,adult,emergence of offspring (adult percentage),number of male offspring,survival,fertility,include,cor,0,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-178530584,table 3 fitness component,survival,fertility,genotype,0,33,1,0,female,cross,Insecta,between
2636,Trichogramma minutum,7,rayyan-178530584,Measurement and selection of parasitoid quality for mass-reared Trichogramma minutum riley used in inundative release,2000,1988-1992,"Ontario, Canada",lab,female,female,660,660,33,33,660,660,660,660,NA,NA,line_mean_correlation,genetic_line,yes,broad,authors,adult,adult,number of female offspring,number of male offspring,fertility,fertility,include,cor,0.339,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-178530584,table 3 fitness component,fertility,fertility,genotype,0.352962253,33,1,0.352962253,female,adult,Insecta,within
2639,Trichogramma minutum,7,rayyan-178530584,Measurement and selection of parasitoid quality for mass-reared Trichogramma minutum riley used in inundative release,2000,1988-1992,"Ontario, Canada",lab,female,female,660,660,33,33,660,660,660,660,NA,NA,line_mean_correlation,genetic_line,yes,broad,authors,adult,adult,number of parasitized host eggs per female,number of female offspring,fertility,fertility,include,cor,0.71,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-178530584,table 3 fitness component,fertility,fertility,genotype,0.887183863,33,1,0.887183863,female,adult,Insecta,within
2640,Trichogramma minutum,7,rayyan-178530584,Measurement and selection of parasitoid quality for mass-reared Trichogramma minutum riley used in inundative release,2000,1988-1992,"Ontario, Canada",lab,female,female,660,660,33,33,660,660,660,660,NA,NA,line_mean_correlation,genetic_line,yes,broad,authors,adult,adult,number of parasitized host eggs per female,number of male offspring,fertility,fertility,include,cor,0.483,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-178530584,table 3 fitness component,fertility,fertility,genotype,0.526889734,33,1,0.526889734,female,adult,Insecta,within
2642,Trichogramma minutum,7,rayyan-178530584,Measurement and selection of parasitoid quality for mass-reared Trichogramma minutum riley used in inundative release,2000,1988-1992,"Ontario, Canada",lab,female,female,660,660,33,33,660,660,660,660,NA,NA,line_mean_correlation,genetic_line,yes,broad,authors,adult,non_adult,number of parasitized host eggs per female,emergence of offspring (adult percentage),fertility,survival,include,cor,0,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-178530584,table 3 fitness component,fertility,survival,genotype,0,33,1,0,female,cross,Insecta,between
2644,Trichogramma minutum,7,rayyan-178530584,Measurement and selection of parasitoid quality for mass-reared Trichogramma minutum riley used in inundative release,2000,1988-1992,"Ontario, Canada",lab,female,female,660,660,33,33,660,660,660,660,NA,NA,line_mean_correlation,genetic_line,yes,broad,authors,non_adult,adult,emergence of offspring (adult percentage),number of female offspring,survival,fertility,include,cor,0,NA,NA,NA,NA,NA,NA,NA,NA,rayyan-178530584,table 3 fitness component,survival,fertility,genotype,0,33,1,0,female,cross,Insecta,between
2645,Trichogrammatoidea,87,rayyan-697471722,Scope for genetic enhancement of the parasitisation potential of four native strains of Trichogrammatoidea sp. nr. lutea Girault (Hymenoptera: Trichogrammatidae) in Kenya,2007,2001-2005,Kenya,lab,female,female,40,40,4,4,40,40,40,40,NA,NA,line_mean_correlation,genetic_line,no,broad,CC,both,adult,female longevity,number of female offspring,survival,fertility,include,cor,0.9,NA,NA,NA,NA,NA,NA,NA,NA,homogamic,table 3a,survival,fertility,genotype,1.47221949,4,1,1.47221949,female,cross,Insecta,between
2646,Trichogrammatoidea,87,rayyan-697471722,Scope for genetic enhancement of the parasitisation potential of four native strains of Trichogrammatoidea sp. nr. lutea Girault (Hymenoptera: Trichogrammatidae) in Kenya,2007,2001-2028,Kenya,lab,female,female,120,120,4,4,120,120,120,120,NA,NA,family_mean_correlation,full_sib,no,broad,CC,non_adult,adult,emergence (proportion of eggs emerged),number of male offspring,survival,fertility,include,cor,0.92,NA,NA,NA,NA,NA,NA,NA,NA,heterogamic,table 3b,survival,fertility,family,1.589026915,120,1,1.589026915,female,cross,Insecta,between
2647,Trichogrammatoidea,87,rayyan-697471722,Scope for genetic enhancement of the parasitisation potential of four native strains of Trichogrammatoidea sp. nr. lutea Girault (Hymenoptera: Trichogrammatidae) in Kenya,2007,2001-2006,Kenya,lab,female,female,40,40,4,4,40,40,40,40,NA,NA,line_mean_correlation,genetic_line,no,broad,CC,both,adult,female longevity,number of male offspring,survival,fertility,include,cor,0.87,NA,NA,NA,NA,NA,NA,NA,NA,homogamic,table 3a,survival,fertility,genotype,1.33307963,4,1,1.33307963,female,cross,Insecta,between
2649,Trichogrammatoidea,87,rayyan-697471722,Scope for genetic enhancement of the parasitisation potential of four native strains of Trichogrammatoidea sp. nr. lutea Girault (Hymenoptera: Trichogrammatidae) in Kenya,2007,2001-2019,Kenya,lab,female,female,120,120,4,4,120,120,120,120,NA,NA,family_mean_correlation,full_sib,no,broad,CC,both,non_adult,female longevity,emergence (% eggs),survival,survival,include,cor,0.49,NA,NA,NA,NA,NA,NA,NA,NA,heterogamic,table 3b,survival,survival,family,0.536060337,120,1,0.536060337,female,cross,Insecta,within
2650,Trichogrammatoidea,87,rayyan-697471722,Scope for genetic enhancement of the parasitisation potential of four native strains of Trichogrammatoidea sp. nr. lutea Girault (Hymenoptera: Trichogrammatidae) in Kenya,2007,2001-2004,Kenya,lab,female,female,40,40,4,4,40,40,40,40,NA,NA,line_mean_correlation,genetic_line,no,broad,CC,both,non_adult,female longevity,emergence (% eggs),survival,survival,include,cor,0.88,NA,NA,NA,NA,NA,NA,NA,NA,homogamic,table 3a,survival,survival,genotype,1.375767657,4,1,1.375767657,female,cross,Insecta,within
2652,Trichogrammatoidea,87,rayyan-697471722,Scope for genetic enhancement of the parasitisation potential of four native strains of Trichogrammatoidea sp. nr. lutea Girault (Hymenoptera: Trichogrammatidae) in Kenya,2007,2001-2003,Kenya,lab,female,female,40,40,4,4,40,40,40,40,NA,NA,line_mean_correlation,genetic_line,no,broad,CC,both,adult,female longevity,fecundity (parasitism),survival,fertility,include,cor,0.74,NA,NA,NA,NA,NA,NA,NA,NA,homogamic,table 3a,survival,fertility,genotype,0.950479381,4,1,0.950479381,female,cross,Insecta,between
2653,Trichogrammatoidea,87,rayyan-697471722,Scope for genetic enhancement of the parasitisation potential of four native strains of Trichogrammatoidea sp. nr. lutea Girault (Hymenoptera: Trichogrammatidae) in Kenya,2007,2001-2023,Kenya,lab,female,female,120,120,4,4,120,120,120,120,NA,NA,family_mean_correlation,full_sib,no,broad,CC,adult,non_adult,fecundity (parasitism),emergence (% eggs),fertility,survival,include,cor,0.89,NA,NA,NA,NA,NA,NA,NA,NA,heterogamic,table 3b,fertility,survival,family,1.421925871,120,1,1.421925871,female,cross,Insecta,between
2655,Trichogrammatoidea,87,rayyan-697471722,Scope for genetic enhancement of the parasitisation potential of four native strains of Trichogrammatoidea sp. nr. lutea Girault (Hymenoptera: Trichogrammatidae) in Kenya,2007,2001-2027,Kenya,lab,female,female,120,120,4,4,120,120,120,120,NA,NA,family_mean_correlation,full_sib,no,broad,CC,non_adult,adult,emergence (proportion of eggs emerged),number of female offspring,survival,fertility,include,cor,0.91,NA,NA,NA,NA,NA,NA,NA,NA,heterogamic,table 3b,survival,fertility,family,1.527524425,120,1,1.527524425,female,cross,Insecta,between
2658,Trichogrammatoidea,87,rayyan-697471722,Scope for genetic enhancement of the parasitisation potential of four native strains of Trichogrammatoidea sp. nr. lutea Girault (Hymenoptera: Trichogrammatidae) in Kenya,2007,2001-2008,Kenya,lab,female,female,40,40,4,4,40,40,40,40,NA,NA,line_mean_correlation,genetic_line,no,broad,CC,adult,non_adult,fecundity (parasitism),emergence (% eggs),fertility,survival,include,cor,0.98,NA,NA,NA,NA,NA,NA,NA,NA,homogamic,table 3a,fertility,survival,genotype,2.297559925,4,1,2.297559925,female,cross,Insecta,between
2659,Trichogrammatoidea,87,rayyan-697471722,Scope for genetic enhancement of the parasitisation potential of four native strains of Trichogrammatoidea sp. nr. lutea Girault (Hymenoptera: Trichogrammatidae) in Kenya,2007,2001-2020,Kenya,lab,female,female,120,120,4,4,120,120,120,120,NA,NA,family_mean_correlation,full_sib,no,broad,CC,both,adult,female longevity,number of female offspring,survival,fertility,include,cor,0.46,NA,NA,NA,NA,NA,NA,NA,NA,heterogamic,table 3b,survival,fertility,family,0.497311288,120,1,0.497311288,female,cross,Insecta,between
2660,Trichogrammatoidea,87,rayyan-697471722,Scope for genetic enhancement of the parasitisation potential of four native strains of Trichogrammatoidea sp. nr. lutea Girault (Hymenoptera: Trichogrammatidae) in Kenya,2007,2001-2015,Kenya,lab,female,female,40,40,4,4,40,40,40,40,NA,NA,line_mean_correlation,genetic_line,no,broad,CC,adult,adult,number of female offspring,number of male offspring,fertility,fertility,include,cor,0.93,NA,NA,NA,NA,NA,NA,NA,NA,homogamic,table 3a,fertility,fertility,genotype,1.65839002,4,1,1.65839002,female,adult,Insecta,within
2662,Trichogrammatoidea,87,rayyan-697471722,Scope for genetic enhancement of the parasitisation potential of four native strains of Trichogrammatoidea sp. nr. lutea Girault (Hymenoptera: Trichogrammatidae) in Kenya,2007,2001-2012,Kenya,lab,female,female,40,40,4,4,40,40,40,40,NA,NA,line_mean_correlation,genetic_line,no,broad,CC,non_adult,adult,emergence (proportion of eggs emerged),number of female offspring,survival,fertility,include,cor,0.97,NA,NA,NA,NA,NA,NA,NA,NA,homogamic,table 3a,survival,fertility,genotype,2.09229572,4,1,2.09229572,female,cross,Insecta,between
2663,Trichogrammatoidea,87,rayyan-697471722,Scope for genetic enhancement of the parasitisation potential of four native strains of Trichogrammatoidea sp. nr. lutea Girault (Hymenoptera: Trichogrammatidae) in Kenya,2007,2001-2024,Kenya,lab,female,female,120,120,4,4,120,120,120,120,NA,NA,family_mean_correlation,full_sib,no,broad,CC,adult,adult,fecundity (parasitism),number of female offspring,fertility,fertility,include,cor,0.97,NA,NA,NA,NA,NA,NA,NA,NA,heterogamic,table 3b,fertility,fertility,family,2.09229572,120,1,2.09229572,female,adult,Insecta,within
2664,Trichogrammatoidea,87,rayyan-697471722,Scope for genetic enhancement of the parasitisation potential of four native strains of Trichogrammatoidea sp. nr. lutea Girault (Hymenoptera: Trichogrammatidae) in Kenya,2007,2001-2021,Kenya,lab,female,female,120,120,4,4,120,120,120,120,NA,NA,family_mean_correlation,full_sib,no,broad,CC,both,adult,female longevity,number of male offspring,survival,fertility,include,cor,0.38,NA,NA,NA,NA,NA,NA,NA,NA,heterogamic,table 3b,survival,fertility,family,0.40005965,120,1,0.40005965,female,cross,Insecta,between
2665,Trichogrammatoidea,87,rayyan-697471722,Scope for genetic enhancement of the parasitisation potential of four native strains of Trichogrammatoidea sp. nr. lutea Girault (Hymenoptera: Trichogrammatidae) in Kenya,2007,2001-2010,Kenya,lab,female,female,40,40,4,4,40,40,40,40,NA,NA,line_mean_correlation,genetic_line,no,broad,CC,adult,adult,fecundity (parasitism),number of male offspring,fertility,fertility,include,cor,0.9,NA,NA,NA,NA,NA,NA,NA,NA,homogamic,table 3a,fertility,fertility,genotype,1.47221949,4,1,1.47221949,female,adult,Insecta,within
2668,Trichogrammatoidea,87,rayyan-697471722,Scope for genetic enhancement of the parasitisation potential of four native strains of Trichogrammatoidea sp. nr. lutea Girault (Hymenoptera: Trichogrammatidae) in Kenya,2007,2001-2025,Kenya,lab,female,female,120,120,4,4,120,120,120,120,NA,NA,family_mean_correlation,full_sib,no,broad,CC,adult,adult,fecundity (parasitism),number of male offspring,fertility,fertility,include,cor,0.94,NA,NA,NA,NA,NA,NA,NA,NA,heterogamic,table 3b,fertility,fertility,family,1.738049345,120,1,1.738049345,female,adult,Insecta,within
2670,Trichogrammatoidea,87,rayyan-697471722,Scope for genetic enhancement of the parasitisation potential of four native strains of Trichogrammatoidea sp. nr. lutea Girault (Hymenoptera: Trichogrammatidae) in Kenya,2007,2001-2009,Kenya,lab,female,female,40,40,4,4,40,40,40,40,NA,NA,line_mean_correlation,genetic_line,no,broad,CC,adult,adult,fecundity (parasitism),number of female offspring,fertility,fertility,include,cor,0.96,NA,NA,NA,NA,NA,NA,NA,NA,homogamic,table 3a,fertility,fertility,genotype,1.945910149,4,1,1.945910149,female,adult,Insecta,within
2671,Trichogrammatoidea,87,rayyan-697471722,Scope for genetic enhancement of the parasitisation potential of four native strains of Trichogrammatoidea sp. nr. lutea Girault (Hymenoptera: Trichogrammatidae) in Kenya,2007,2001-2030,Kenya,lab,female,female,120,120,4,4,120,120,120,120,NA,NA,family_mean_correlation,full_sib,no,broad,CC,adult,adult,number of female offspring,number of male offspring,fertility,fertility,include,cor,0.91,NA,NA,NA,NA,NA,NA,NA,NA,heterogamic,table 3b,fertility,fertility,family,1.527524425,120,1,1.527524425,female,adult,Insecta,within
2672,Trichogrammatoidea,87,rayyan-697471722,Scope for genetic enhancement of the parasitisation potential of four native strains of Trichogrammatoidea sp. nr. lutea Girault (Hymenoptera: Trichogrammatidae) in Kenya,2007,2001-2018,Kenya,lab,female,female,120,120,4,4,120,120,120,120,NA,NA,family_mean_correlation,full_sib,no,broad,CC,both,adult,female longevity,fecundity (parasitism),survival,fertility,include,cor,0.34,NA,NA,NA,NA,NA,NA,NA,NA,heterogamic,table 3b,survival,fertility,family,0.354092529,120,1,0.354092529,female,cross,Insecta,between
2673,Trichogrammatoidea,87,rayyan-697471722,Scope for genetic enhancement of the parasitisation potential of four native strains of Trichogrammatoidea sp. nr. lutea Girault (Hymenoptera: Trichogrammatidae) in Kenya,2007,2001-2013,Kenya,lab,female,female,40,40,4,4,40,40,40,40,NA,NA,line_mean_correlation,genetic_line,no,broad,CC,non_adult,adult,emergence (proportion of eggs emerged),number of male offspring,survival,fertility,include,cor,0.99,NA,NA,NA,NA,NA,NA,NA,NA,homogamic,table 3a,survival,fertility,genotype,2.646652412,4,1,2.646652412,female,cross,Insecta,between
2675,Trichoplusia ni,18,rayyan-687940426,Genetic variation in fitness parameters associated with resistance to Bacillus thuringiensis in male and female Trichoplusia ni,2011,2001,"British Columbia, Canada",lab,male,male,48,48,NA,NA,48,48,48,48,1440,1440,family_mean_correlation,full_sib,yes,broad,CC,non_adult,non_adult,time to pupation,pupal weight,reverse_maturation,size,include,cor,-0.34,NA,NA,NA,NA,NA,NA,NA,NA,male,table 5,maturation,size,family,-0.354092529,48,-1,0.354092529,male,non_adult,Insecta,between
2676,Trichoplusia ni,18,rayyan-687940426,Genetic variation in fitness parameters associated with resistance to Bacillus thuringiensis in male and female Trichoplusia ni,2011,2001,"British Columbia, Canada",lab,female,female,48,48,NA,NA,48,48,48,48,1440,1440,family_mean_correlation,full_sib,yes,broad,CC,non_adult,non_adult,time to pupation,pupal weight,reverse_maturation,size,include,cor,-0.15,NA,NA,NA,NA,NA,NA,NA,NA,female,table 5,maturation,size,family,-0.151140436,48,-1,0.151140436,female,non_adult,Insecta,between
2677,Tropidonophis mairii,138,rayyan-697472208,Repeatability and heritability of reproductive traits in free-ranging snakes,2007,1998-2003,"Fogg Dam Conservation Reserve, Darwin, Autralia",lab,both,female,59,59,NA,NA,59,59,NA,NA,NA,NA,parent_offspring_regression,parent_offspring_pair,no,narrow,authors,non_adult,adult,relative clutch mass (to maternal size),post-partum condition (mass relative to length),size,size,include,cor,0.44,2.3,se,NA,NA,NA,NA,NA,NA,rayyan-697472208,table 3,size,size,family,0.472230804,59,1,0.472230804,female,cross,Lepidosauria,within
2678,Tropidonophis mairii,138,rayyan-697472208,Repeatability and heritability of reproductive traits in free-ranging snakes,2007,1998-2003,"Fogg Dam Conservation Reserve, Darwin, Autralia",lab,female,female,59,59,NA,NA,59,59,NA,NA,NA,NA,parent_offspring_regression,parent_offspring_pair,no,narrow,authors,adult,adult,clutch size,post-partum condition (mass relative to length),fertility,size,include,cor,-0.32,2.14,se,NA,NA,NA,NA,NA,NA,rayyan-697472208,table 3,fertility,size,family,-0.331647109,59,1,-0.331647109,female,adult,Lepidosauria,between
2679,Tropidonophis mairii,138,rayyan-697472208,Repeatability and heritability of reproductive traits in free-ranging snakes,2007,1998-2003,"Fogg Dam Conservation Reserve, Darwin, Autralia",lab,both,both,59,59,NA,NA,59,59,NA,NA,NA,NA,parent_offspring_regression,parent_offspring_pair,no,narrow,authors,non_adult,non_adult,egg mass,relative clutch mass (to maternal size),size,size,include,cor,NA,2.18,se,NA,NA,NA,NA,NA,NA,rayyan-697472208,table 3,size,size,family,NA,59,1,NA,both,non_adult,Lepidosauria,within
2680,Tropidonophis mairii,138,rayyan-697472208,Repeatability and heritability of reproductive traits in free-ranging snakes,2007,1998-2003,"Fogg Dam Conservation Reserve, Darwin, Autralia",lab,female,both,59,59,NA,NA,59,59,NA,NA,NA,NA,parent_offspring_regression,parent_offspring_pair,no,narrow,authors,adult,non_adult,clutch size,relative clutch mass (to maternal size),fertility,size,include,cor,-0.9,3.82,se,NA,NA,NA,NA,NA,NA,rayyan-697472208,table 3,fertility,size,family,-1.47221949,59,1,-1.47221949,female,cross,Lepidosauria,between
2681,Tropidonophis mairii,138,rayyan-697472208,Repeatability and heritability of reproductive traits in free-ranging snakes,2007,1998-2003,"Fogg Dam Conservation Reserve, Darwin, Autralia",lab,both,female,59,59,NA,NA,59,59,NA,NA,NA,NA,parent_offspring_regression,parent_offspring_pair,no,narrow,authors,non_adult,adult,egg mass,clutch size,size,fertility,include,cor,-0.6,1.35,se,NA,NA,NA,NA,NA,NA,rayyan-697472208,table 3,size,fertility,family,-0.693147181,59,1,-0.693147181,female,cross,Lepidosauria,between
2682,Tropidonophis mairii,138,rayyan-697472208,Repeatability and heritability of reproductive traits in free-ranging snakes,2007,1998-2003,"Fogg Dam Conservation Reserve, Darwin, Autralia",lab,both,female,59,59,NA,NA,59,59,NA,NA,NA,NA,parent_offspring_regression,parent_offspring_pair,no,narrow,authors,non_adult,adult,egg mass,post-partum condition (mass relative to length),size,size,include,cor,0.89,0.95,se,NA,NA,NA,NA,NA,NA,rayyan-697472208,table 3,size,size,family,1.421925871,59,1,1.421925871,female,cross,Lepidosauria,within
2683,Xiphophorus birchmanni,163,rayyan-197246987,"Phenotypic and genetic integration of personality and growth under competition in the sheepshead swordtail, Xiphophorus birchmanni",2018,2010-2011,"Hidalgo, Mexico",lab,both,both,61,61,NA,NA,32,32,19,19,384,384,animal_model,pedigree,no,narrow,authors,adult,adult,weight,standard length,size,size,include,cor,0.852,0.093,se,NA,NA,NA,NA,NA,NA,rayyan-197246987,table 4,size,size,pedigree,1.263404571,384,1,1.263404571,both,adult,Actinopteri,within
2684,Xiphophorus birchmanni,45,rayyan-697471378,"Sex-specific plasticity and genotype × sex interactions for age and size of maturity in the sheepshead swordtail, Xiphophorus birchmanni",2016,2010,"Arroyo Coacuilco river, Mexico",lab,male,male,61,61,NA,NA,32,32,19,19,368,368,animal_model,full/half_sib,no,narrow,authors,adult,adult,weight at maturity,size at maturity,size,size,include,cor,0.892,0.087,se,NA,NA,NA,NA,NA,NA,male,table 3,size,size,family,1.431629261,61,1,1.431629261,male,adult,Actinopteri,within
2685,Xiphophorus birchmanni,45,rayyan-697471378,"Sex-specific plasticity and genotype × sex interactions for age and size of maturity in the sheepshead swordtail, Xiphophorus birchmanni",2016,2010,"Arroyo Coacuilco river, Mexico",lab,male,male,61,61,NA,NA,32,32,19,19,384,368,animal_model,full/half_sib,no,narrow,authors,non_adult,adult,age at maturity,weight at maturity,reverse_maturation,size,include,cor,-0.027,0.518,se,NA,NA,NA,NA,NA,NA,male,table 3,maturation,size,family,-0.027006564,61,-1,0.027006564,male,cross,Actinopteri,between
2686,Xiphophorus birchmanni,45,rayyan-697471378,"Sex-specific plasticity and genotype × sex interactions for age and size of maturity in the sheepshead swordtail, Xiphophorus birchmanni",2016,2010,"Arroyo Coacuilco river, Mexico",lab,female,female,61,61,NA,NA,32,32,19,19,384,368,animal_model,full/half_sib,no,narrow,authors,non_adult,adult,age at maturity,weight at maturity,reverse_maturation,size,include,cor,0.41,0.33,se,NA,NA,NA,NA,NA,NA,female,table 3,maturation,size,family,0.435611223,61,-1,-0.435611223,female,cross,Actinopteri,between
2687,Xiphophorus birchmanni,163,rayyan-197246987,"Phenotypic and genetic integration of personality and growth under competition in the sheepshead swordtail, Xiphophorus birchmanni",2018,2010-2011,"Hidalgo, Mexico",lab,both,both,61,61,NA,NA,32,32,19,19,384,384,animal_model,pedigree,no,narrow,authors,adult,adult,growth in weight,growth in standard length,growth,growth,include,cor,0.89,0.072,se,NA,NA,NA,NA,NA,NA,rayyan-197246987,table 4,growth,growth,pedigree,1.421925871,384,1,1.421925871,both,adult,Actinopteri,within
2688,Xiphophorus birchmanni,45,rayyan-697471378,"Sex-specific plasticity and genotype × sex interactions for age and size of maturity in the sheepshead swordtail, Xiphophorus birchmanni",2016,2010,"Arroyo Coacuilco river, Mexico",lab,male,male,61,61,NA,NA,32,32,19,19,384,368,animal_model,full/half_sib,no,narrow,authors,non_adult,adult,age at maturity,size at maturity,reverse_maturation,size,include,cor,-0.029,0.499,se,NA,NA,NA,NA,NA,NA,male,table 3,maturation,size,family,-0.029008134,61,-1,0.029008134,male,cross,Actinopteri,between
2689,Xiphophorus birchmanni,45,rayyan-697471378,"Sex-specific plasticity and genotype × sex interactions for age and size of maturity in the sheepshead swordtail, Xiphophorus birchmanni",2016,2010,"Arroyo Coacuilco river, Mexico",lab,female,female,61,61,NA,NA,32,32,19,19,368,368,animal_model,full/half_sib,no,narrow,authors,adult,adult,weight at maturity,size at maturity,size,size,include,cor,0.987,0.025,se,NA,NA,NA,NA,NA,NA,female,table 3,size,size,family,2.514715943,61,1,2.514715943,female,adult,Actinopteri,within
2690,Xiphophorus birchmanni,163,rayyan-197246987,"Phenotypic and genetic integration of personality and growth under competition in the sheepshead swordtail, Xiphophorus birchmanni",2018,2010-2011,"Hidalgo, Mexico",lab,both,both,61,61,NA,NA,32,32,19,19,384,384,animal_model,pedigree,no,narrow,authors,adult,adult,growth in weight,standard length,growth,size,include,cor,-0.08,0.362,se,NA,NA,NA,NA,NA,NA,rayyan-197246987,table 4,growth,size,pedigree,-0.080171325,384,1,-0.080171325,both,adult,Actinopteri,between
2691,Xiphophorus birchmanni,163,rayyan-197246987,"Phenotypic and genetic integration of personality and growth under competition in the sheepshead swordtail, Xiphophorus birchmanni",2018,2010-2011,"Hidalgo, Mexico",lab,both,both,61,61,NA,NA,32,32,19,19,384,384,animal_model,pedigree,no,narrow,authors,adult,adult,growth in weight,weight,growth,size,include,cor,0.367,0.313,se,NA,NA,NA,NA,NA,NA,rayyan-197246987,table 4,growth,size,pedigree,0.384951707,384,1,0.384951707,both,adult,Actinopteri,between
2692,Xiphophorus birchmanni,163,rayyan-197246987,"Phenotypic and genetic integration of personality and growth under competition in the sheepshead swordtail, Xiphophorus birchmanni",2018,2010-2011,"Hidalgo, Mexico",lab,both,both,61,61,NA,NA,32,32,19,19,384,384,animal_model,pedigree,no,narrow,authors,adult,adult,growth in standard length,weight,growth,size,include,cor,0.118,0.346,se,NA,NA,NA,NA,NA,NA,rayyan-197246987,table 4,growth,size,pedigree,0.118552299,384,1,0.118552299,both,adult,Actinopteri,between
2693,Xiphophorus birchmanni,45,rayyan-697471378,"Sex-specific plasticity and genotype × sex interactions for age and size of maturity in the sheepshead swordtail, Xiphophorus birchmanni",2016,2010,"Arroyo Coacuilco river, Mexico",lab,female,female,61,61,NA,NA,32,32,19,19,384,368,animal_model,full/half_sib,no,narrow,authors,non_adult,adult,age at maturity,size at maturity,reverse_maturation,size,include,cor,0.361,0.318,se,NA,NA,NA,NA,NA,NA,female,table 3,maturation,size,family,0.378035274,61,-1,-0.378035274,female,cross,Actinopteri,between
2694,Xiphophorus birchmanni,163,rayyan-197246987,"Phenotypic and genetic integration of personality and growth under competition in the sheepshead swordtail, Xiphophorus birchmanni",2018,2010-2011,"Hidalgo, Mexico",lab,both,both,61,61,NA,NA,32,32,19,19,384,384,animal_model,pedigree,no,narrow,authors,adult,adult,growth in standard length,standard length,growth,size,include,cor,-0.176,0.33,se,NA,NA,NA,NA,NA,NA,rayyan-197246987,table 4,growth,size,pedigree,-0.177851799,384,1,-0.177851799,both,adult,Actinopteri,between
NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA