Author,Year,Title,Journal,SC_metrics,in_Lowry_2008,parents_different_ploidy,Genus,Taxa_type,Taxa_type2,Family,Species1,Species2,sympatric_at_least_some_pops,geography,temperate_tropical,Life_History,Life_History2,Lifeform,Ecogeo1,Ecogeo2,Ecogeo1_ecogeo,Ecogeo2_ecogeo,Ecogeo1_micro,Ecogeo2_micro,ImmigrantInviability1,ImmigrantInviability2,Pheno1,Pheno2,MatingSystem1,MatingSystem2,DifferentialPollen1,DifferentialPollen2,FloralIsolation1,FloralIsolation2,FloralIsolation1_pollinators,FloralIsolation2_pollinators,FloralIsolation1_transitions,FloralIsolation2_transitions,FloralIsolation1_deposition,FloralIsolation2_deposition,PollenPistil1,PollenPistil2,FruitProduction1,FruitProduction2,SeedProduction1,SeedProduction2,F1Germination1,F1Germination2,F1Viability1,F1Viability2,F1PollenSterility1,F1PollenSterility2,F1OvuleFertility1,F1OvuleFertility2,ExtrinsicPost1,ExtrinsicPost2
Arida et al.,2021,Reproductive barriers and fertility of two neotropical orchid species and their natural hybrid,Evolutionary Ecology,YES,NO,NO,Epidendrum,species,species,Orchidaceae,Epidendrum denticulatum,Epidendrum orchidiflorum,sympatric,sympatric,tropical,perennial,perennial,herb,0.57,0.7,NA,NA,0.57,0.7,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,0.06,0.19,NA,NA,0.08,-0.01,NA,NA,NA,NA,0.23,0.25,0.23,0.25,0,0.622
Borchsenius et al.,2016,Reproductive isolation of sympatric forms of the understorey palm Geonoma macrostachys in western Amazonia,Botanical Journal of the Linnean Society,NO,NO,NO,Geonoma,ecotypes,ecotypes,Arecaceae,Geonoma macrostachys (short morph),Geonoma macrostachys (large morph),sympatric,sympatric,tropical,perennial,perennial,shrub,0.156,0.409,NA,NA,0.156,0.409,NA,NA,0.881,0.924,NA,NA,NA,NA,0,0.083,0,0.083,NA,NA,NA,NA,NA,NA,-0.106,0.06,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA
Briscoe Runquist et al.,2014,RAPID EVOLUTION OF REPRODUCTIVE ISOLATION BETWEEN INCIPIENT OUTCROSSING AND SELFING CLARKIA SPECIES,Evolution,YES,NO,NO,Clarkia,subspecies,ecotypes,Onagraceae,Clarkia xantiana ssp. parviflora,Clarkia xantiana ssp. xantiana,sympatric,sympatric,temperate,annual,annual,herb,0.565,0.573,0.565,0.573,NA,NA,NA,NA,0.959,0.785,NA,NA,-0.663,0.663,0.76,0.76,0.76,0.76,0.0639,-0.0384,NA,NA,-0.117,0.142,NA,NA,0.06,0.22,NA,NA,0.098,-0.008,-0.077,0.102,NA,NA,NA,NA
Brys et al.,2013,THE CONTRIBUTION OF MATING SYSTEM VARIATION TO REPRODUCTIVE ISOLATION IN TWO CLOSELY RELATED CENTAURIUM SPECIES (GENTIANACEAE) WITH A GENERALIZED FLOWER MORPHOLOGY,Evolution,NO,NO,NO,Centaurium,species,species,Gentianaceae,Centaurium erythraea,Centaurium littorale,sympatric,sympatric,temperate,biennial,biennial,herb,NA,NA,NA,NA,NA,NA,NA,NA,0.322,0.309,NA,NA,0.459,-0.459,0.51,-0.266,NA,NA,NA,NA,0.51,-0.266,0.18,0.914,NA,NA,0.365,0.175,0.152,0.28,0.337,0.521,0.926,0.427,0.799,0.51,NA,NA
Brys et al.,2016,The importance of autonomous selfing in preventing hybridizaton in three closely related plant species,Journal of Ecology,YES,NO,NO,Centaurium,species,species,Gentianaceae,Centaurium erythraea,Centaurium littorale,sympatric,sympatric,temperate,biennial,biennial,herb,NA,NA,NA,NA,NA,NA,NA,NA,0.03,0.11,-0.404,0.41,0.463,-0.463,0.455,0.2,0.455,0.2,NA,NA,NA,NA,NA,NA,NA,NA,0.288,0.027,0.152,0.28,0.335,0.56,NA,NA,NA,NA,NA,NA
Brys et al.,2016,The importance of autonomous selfing in preventing hybridizaton in three closely related plant species,Journal of Ecology,YES,NO,NO,Centaurium,species,species,Gentianaceae,Centaurium erythraea,Centaurium pulchellum,sympatric,sympatric,temperate,"biennial, annual",A / B / P,herb,NA,NA,NA,NA,NA,NA,NA,NA,0.209,0.284,-0.246,0.75,0.672,-0.672,0.545,0,0.545,0,NA,NA,NA,NA,NA,NA,NA,NA,0.426,0.376,0.249,0.792,0.047,0.016,NA,NA,NA,NA,NA,NA
Brys et al.,2016,The importance of autonomous selfing in preventing hybridizaton in three closely related plant species,Journal of Ecology,YES,NO,NO,Centaurium,species,species,Gentianaceae,Centaurium littorale,Centaurium pulchellum,sympatric,sympatric,temperate,"biennial, annual",A / B / P,herb,NA,NA,NA,NA,NA,NA,NA,NA,0.164,0.176,0.273,0.667,0.302,-0.302,0.467,0.2,0.467,0.2,NA,NA,NA,NA,NA,NA,NA,NA,0.077,0.5,0.414,0.712,0.133,0.141,NA,NA,NA,NA,NA,NA
Burge et al.,2013,LIMITED HYBRIDIZATION ACROSS AN EDAPHIC DISJUNCTION BETWEEN THE GABBRO-ENDEMIC SHRUB CEANOTHUS RODERICKII (RHAMNACEAE) AND THE SOIL-GENERALIST CEANOTHUS CUNEATUS,American Journal of Botany,NO,NO,NO,Ceanothus,species,species,Rhamnaceae,Ceanothus roderickii ,Ceanothus cuneatus,peripatric,parapatric,temperate,perennial,perennial,shrub,NA,NA,NA,NA,NA,NA,-0.067,0.333,0,0.378,NA,NA,NA,NA,0.476,0.633,0.476,0.633,NA,NA,NA,NA,NA,NA,-1,-1,-1,-1,NA,NA,0.004,0.171,NA,NA,NA,NA,0.35,0.176
Cahenzli et al.,2018,Divergent strategies in pre- and postzygotic reproductive isolation between two closely related Dianthus species,Evolution,YES,NO,NO,Dianthus,species,species,Caryophyllaceae,Dianthus carthusianorum,Dianthus sylvestris,sympatric / parapatric,parapatric,temperate,perennial,perennial,herb,0.628,0.49,0.628,0.49,NA,NA,0.262,0.862,NA,NA,NA,NA,NA,NA,0.76,0.468,NA,NA,0.76,0.468,NA,NA,NA,NA,0.21,0.104,0.312,-0.176,-0.003,0.003,-0.017,-0.009,NA,NA,NA,NA,0.279,0.59
Cai et al.,2019,Parallel Speciation of Wild Rice Associated with Habitat Shifts,Molecular Biology and Evolution,NO,NO,NO,Oryza,species,species,Poaceae,Oryza nivara ,Oryza rufipogon,sympatric,sympatric,tropical,"annual, perennial",A / B / P,grass,NA,NA,NA,NA,NA,NA,NA,NA,1,1,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,-0.227,1,NA,NA,-0.143,-0.253,NA,NA,NA,NA,NA,NA
Campbell and Waser,2001,Genotype-by-environment interaction and the fitness of plant hybrids in the wild,Evolution,NO,NO,NO,Ipomopsis,species,species,Polemoniaceae,Ipomopsis aggregata,Ipomopsis tenuituba,sympatric,sympatric,temperate,perennial,perennial,herb,NA,NA,NA,NA,NA,NA,0.161,0.684,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,0.2,0.003,NA,NA,NA,NA,NA,NA,NA,NA,0.208,0.594
Carrio and Guemes,2014,The effectiveness of pre- and post-zygotic barriers in avoiding hybridization between two snapdragons (Antirrhinum L.: Plantaginaceae),Botanical Journal of the Linnean Society,NO,NO,NO,Antirrhinum,species,species,Plantaginaceae,Antirrhinum valentinum ,Antirrhinum controversum,sympatric,sympatric,temperate,perennial,perennial,herb,NA,NA,NA,NA,NA,NA,NA,NA,0.719,0.432,NA,NA,NA,NA,0.667,0.813,NA,NA,0.667,0.813,NA,NA,0.212,0.112,0.038,0.366,0.326,0.536,1,0.171,NA,NA,NA,NA,0.422,0.355,NA,NA
Castro et al.,2020,The role of multiple reproductive barriers: strong post-pollination interactions govern cytotype isolation in a tetraploid–octoploid contact zone,Annals of Botany,NO,NO,YES,Gladiolus,cytotypes,cytotypes,Iridaceae,Gladiolus communis (tetraploid),Gladiolus communis (octaploid),sympatric,parapatric,temperate,perennial,perennial,herb,NA,NA,NA,NA,NA,NA,NA,NA,0.154,0.157,NA,NA,NA,NA,-0.49,-0.49,NA,NA,-0.49,-0.49,NA,NA,0.197,0.243,0.027,-0.011,0.25,0.16,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA
Chari and Wilson,2001,Factors limiting hybridization between Penstemon spectabilis and Penstemon centranthifolius,Canadian Journal of Botany,NO,YES,NO,Penstemon,species,species,Plantaginaceae,Penstemon spectabilis ,Penstemon centranthifolius,sympatric,sympatric,temperate,perennial,perennial,shrub,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,0,0.643,0,0.643,NA,NA,NA,NA,0.197,0.177,0.134,0.929,0.232,NA,NA,NA,0.017,NA,NA,NA,NA,NA,NA,NA
Chen,2013,Sexual isolation in two bee-pollinated Costus (Costaceae),Plant Reproduction,NO,NO,NO,Costus,species,species,Costaceae,Costus allenii,Costus villosissimus,closely parapatric (within flight distances),parapatric,tropical,perennial,perennial,herb,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,0,0.446,NA,NA,-0.366,0.446,0,0.319,0.74,0.36,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA
Christie and Strauss,2019,Reproductive isolation and the maintenance of species boundaries in two serpentine endemic Jewelflowers,Evolution,YES,NO,NO,Streptanthus,species,species,Brassicaceae,Streptanthus breweri ,Streptanthus hesperidis,sympatric,sympatric,temperate,annual,annual,herb,0.647,0.601,NA,NA,0.647,0.601,NA,NA,0.267,0.22,NA,NA,NA,NA,0.472,0.383,0.472,0.383,NA,NA,NA,NA,NA,NA,0,0,0.876,0,NA,NA,0.364,0.177,0.905,0.998,0.842,0.622,NA,NA
Coetzee et al.,2020,Post‐pollination barriers enable coexistence of pollinator‐sharing ornithophilous Erica species ,Journal of Plant Research,YES,NO,NO,Erica,species,species,Ericaceae,Erica plukenetii,Erica coccinea,sympatric,sympatric,temperate,perennial,perennial,shrub,0.38,0.27,0.38,0.27,NA,NA,NA,NA,0.91,0.91,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,0.76,0.8,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA
Costa et al.,2007,Post-zygotic Reproductive Isolation Between Sympatric Taxa in the Chamaecrista desvauxii Complex (Leguminosae–Caesalpinioideae),Annals of Botany,NO,YES,NO,Chamaecrista,subspecies,ecotypes,Fabaceae,Chamaecrista desvauxii var. graminea ,Chamaecrista desvauxii var. latistipula,sympatric,sympatric,tropical,"annual, perennial",A / B / P,herb,NA,NA,NA,NA,NA,NA,NA,NA,0.027,0.638,NA,NA,NA,NA,0.006,0,0.006,0,NA,NA,NA,NA,NA,NA,-0.101,0.102,1,1,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA
Cuevas et al.,2018,"Reproductive isolation between Salvia elegans and S. fulgens, two hummingbird-pollinated sympatric sages",Plant Biology,NO,NO,NO,Salvia,species,species,Lamiaceae,Salvia elegans ,Salvia fulgens,sympatric,sympatric,tropical,perennial,perennial,shrub,0.776,0.371,0.776,0.371,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,0.89,0.965,0.89,0.965,NA,NA,NA,NA,NA,NA,0.509,0.89,0.428,0.079,0.048,1,NA,NA,NA,NA,NA,NA,NA,NA
Dell'Olivo et al.,2011,ISOLATION BARRIERS BETWEEN PETUNIA AXILLARIS AND PETUNIA INTEGRIFOLIA (SOLANACEAE),Evolution,NO,NO,NO,Petunia,species,species,Solanaceae,Petunia integrifolia ,Petunia axillaris,mostly allopatric (very few sympatric),sympatric,temperate,perennial,perennial,herb,0.892,0.981,0.892,0.981,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,1,0.538,NA,NA,1,0.538,NA,NA,1,0.467,0.908,0.702,0.86,0.546,-0.275,0.312,NA,NA,0.132,0.152,-0.052,0.696,0.576,0.244
Emms and Arnold,1997,THE EFFECT OF HABITAT ON PARENTAL AND HYBRID FITNESS: TRANSPLANT EXPERIMENTS WITH LOUISIANA IRISES,Evolution,NO,YES,NO,Iris,species,species,Iridaceae,Iris fulva,Iris hexagona,sympatric,sympatric,temperate,perennial,perennial,herb,NA,NA,NA,NA,NA,NA,0.035,0.05,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,-0.023,-0.019
Fachardo and Sigrist,2020,Pre-zygotic reproductive isolation between two synchronopatric Opuntia (Cactaceae) species int he Brazilian Chaco,Plant Biology,NO,NO,NO,Opuntia,species,species,Cactaceae,Opuntia elata,Opuntia retrorsa,sympatric,sympatric,tropical,perennial,perennial,shrub,NA,NA,NA,NA,NA,NA,NA,NA,0.5,0.205,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,0.272,-0.013,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA
Gervasi et al.,2017,Floral scent and species divergence in a pair of sexually deceptive orchids,Ecology and Evolution,NO,NO,NO,Ophrys,species,species,Orchidaceae,Ophrys insectifera ,Ophrys aymoninii,sympatric,sympatric,temperate,perennial,perennial,herb,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,1,1,NA,NA,NA,NA,1,1,NA,NA,-0.143,0,-0.045,0,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA
Hersch-Green,2012,Polyploidy in Indian Paintbrush (Castilleja: Orobanchaceae) species shapes but does not prevent gene flow across species boundaries ,American Journal of Botany,NO,NO,YES,Castilleja,cytotypes,cytotypes,Orobanchaceae,Castilleja miniata (octoploid),Castilleja rhexifolia (tetraploid),sympatric,sympatric,temperate,perennial,perennial,herb,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,0.091,0.6,NA,NA,0.091,0.6,NA,NA,NA,NA,0.101,0.185,0.452,0.159,0.286,0.294,NA,NA,NA,NA,NA,NA,NA,NA
Hersch-Green,2012,Polyploidy in Indian Paintbrush (Castilleja: Orobanchaceae) species shapes but does not prevent gene flow across species boundaries ,American Journal of Botany,NO,NO,YES,Castilleja,cytotypes,cytotypes,Orobanchaceae,Castilleja miniata (octoploid),Castilleja sulphurea (diploid),sympatric,sympatric,temperate,perennial,perennial,herb,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,0.6,0.959,NA,NA,0.6,0.959,NA,NA,NA,NA,0.108,0.197,0.442,0.193,0.742,0.357,NA,NA,NA,NA,NA,NA,NA,NA
Hersch-Green,2012,Polyploidy in Indian Paintbrush (Castilleja: Orobanchaceae) species shapes but does not prevent gene flow across species boundaries ,American Journal of Botany,NO,NO,YES,Castilleja,cytotypes,cytotypes,Orobanchaceae,Castilleja rhexifolia (tetraploid),Castilleja sulphurea (diploid),sympatric,sympatric,temperate,perennial,perennial,herb,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,0.114,0.157,NA,NA,0.114,0.157,NA,NA,NA,NA,0.318,0.082,0.119,0.084,0.833,0.52,NA,NA,NA,NA,NA,NA,NA,NA
Hipperson et al.,2016,Ecological speciation in sympatric palms: 2. Pre- and post-zygotic isolation,Journal of Evolutionary Biology,NO,NO,NO,Howea,species,species,Arecaceae,Howea belmoreana ,Howea forsteriana,sympatric,sympatric,temperate,perennial,perennial,tree,NA,NA,NA,NA,NA,NA,0.545,-0.054,0.807,0.806,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,-0.023,-0.055
Ishizaki et al.,2013,Mechanisms of reproductive isolation of interspecific hybridization between Trillium camschatcense and T. tschonoskii (Melanthiaceae),Plant Species Biology,NO,NO,NO,Trillium,species,species,Melanthiaceae,Trillium camschatcense ,Trillium tschonoskii,sympatric,sympatric,temperate,perennial,perennial,herb,NA,NA,NA,NA,NA,NA,NA,NA,0.158,0.295,0.096,0.474,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,0.731,0.981,NA,NA,NA,NA,NA,NA,-0.438,1,NA,NA,NA,NA,NA,NA
Jacquemyn et al.,2017,Immigrant and extrinsic hybrid seed inviability contribute to reproductive isolation between forest and dune ecotypes of Epipactis helleborine (Orchidaceae),Oikos,NO,NO,NO,Epipactis,ecotypes,ecotypes,Orchidaceae,Epipactis helleborine (dune),Epipactis helleborine (forest),allopatric,allopatric,temperate,perennial,perennial,herb,NA,NA,NA,NA,NA,NA,1,0.644,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,0.009,-0.016,0.102,0.017,NA,NA,-0.139,-0.233,NA,NA,NA,NA,0.306,0.3
Johnson et al.,2015,Postzygotic barriers isolate sympatric species of Cyrtandra (Gesneriaceae) in Hawaiian montane forest understories,American Journal of Botany,YES,NO,NO,Cyrtandra,species,species,Gesneriaceae,Cyrtandra kauaiensis,Cyrtandra longifolia,sympatric,sympatric,tropical,perennial,perennial,shrub,0,0.563,0,0.563,NA,NA,NA,NA,0.066,0.106,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,0.044,0,-0.043,-0.306,NA,NA,0.501,0.575,0.236,0.184,NA,NA,NA,NA,NA,NA
Johnson et al.,2015,Postzygotic barriers isolate sympatric species of Cyrtandra (Gesneriaceae) in Hawaiian montane forest understories,American Journal of Botany,YES,NO,NO,Cyrtandra,species,species,Gesneriaceae,Cyrtandra paludosa,Cyrtandra platyphylla,sympatric,sympatric,tropical,perennial,perennial,shrub,0.159,0.413,0.159,0.413,NA,NA,NA,NA,0.697,0.066,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,0,-0.023,0.011,-0.158,NA,NA,0.056,0.535,-0.089,0.788,NA,NA,NA,NA,NA,NA
Karrenberg et al.,2018,Ecological divergence plays an important role in strong but complex reproductive isolation in campions (Silene),Evolution,YES,NO,NO,Silene,species,species,Caryophyllaceae,Silene dioica ,Silene latifolia,(partially) sympatric; many experiments and population pairs,sympatric,temperate,"biennial, perennial",A / B / P,herb,0.132,0.615,0.132,0.615,NA,NA,0.722,0.472,0.399,0.365,NA,NA,NA,NA,0.469,0.295,NA,NA,NA,NA,0.469,0.295,-0.031,0.632,NA,NA,0.007,0.09,NA,NA,NA,NA,0.172,0.28,-0.105,0.065,0.499,0.304
Kay,2006,REPRODUCTIVE ISOLATION BETWEEN TWO CLOSELY RELATED HUMMINGBIRD- POLLINATED NEOTROPICAL GINGERS,Evolution,NO,YES,NO,Costus,species,species,Costaceae,Costus pulverulentus ,Costus scaber,sympatric,sympatric,tropical,perennial,perennial,herb,0.348,0.478,0.348,0.478,0.129,0.438,NA,NA,0.103,0.394,NA,NA,NA,NA,1,0.743,0,0.743,NA,NA,1,0.727,0.98,0.708,NA,NA,0.953,0.674,-0.185,0.684,NA,NA,0.016,-0.008,NA,NA,NA,NA
Keller et al.,2016,Both morph- and species-dependent asymmetries affect reproductive barriers between heterostylous species,Ecology and Evolution,YES,NO,NO,Primula,species,species,Primulaceae,Primula elatior (L + S morphs),Primula vulgaris (L + S morphs),sympatric,sympatric,temperate,perennial,perennial,herb,0.827,0.59,0.827,0.59,NA,NA,NA,NA,0.237,0.417,NA,NA,NA,NA,-0.087,0.011,NA,NA,NA,NA,-0.087,0.011,NA,NA,-0.003,0.229,0.233,0.591,NA,NA,0.054,-0.097,-0.106,0.193,-0.012,0.27,NA,NA
Keller et al.,2020,Asymmetries of reproductive isolation are reflected in directionalities of hybridication: integrative evidence on the ocmplexity of species boundaries,New Phytologist,YES,NO,NO,Primula,species,species,Primulaceae,Primula veris,Primula vulgaris,sympatric,sympatric,temperate,perennial,perennial,herb,NA,NA,NA,NA,NA,NA,NA,NA,0.244,0.29,NA,NA,NA,NA,0.277,0.734,NA,NA,0.277,0.734,NA,NA,NA,NA,NA,NA,0.104,0.317,0.295,0.37,NA,NA,NA,NA,NA,NA,NA,NA
Koelling and Mauricio,2010,GENETIC FACTORS ASSOCIATED WITH MATING SYSTEM CAUSE A PARTIAL REPRODUCTIVE BARRIER BETWEEN TWO PARAPATRIC SPECIES OF LEAVENWORTHIA (BRASSICACEAE),American Journal of Botany,NO,NO,NO,Leavenworthia,species,species,Brassicaceae,Leavenworthia alabamica,Leavenworthia crassa,parapatric,parapatric,temperate,annual,annual,herb,NA,NA,NA,NA,NA,NA,-0.002,-0.001,NA,NA,-0.048,-0.048,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,-0.038,0,NA,NA,NA,NA,0.021,0.014,NA,NA,0.062,0.251
Liang et al.,2018,Impact of pre- and post-pollination barriers on pollen transfer and reproductive isolation among three sympatric Pedicularis (Orobanchaceae) species,Plant Biology,YES,NO,NO,Pedicularis,species,species,Orobanchaceae,Pedicularis gruina,Pedicularis tenuisecta,sympatric,sympatric,temperate,perennial,perennial,herb,NA,NA,NA,NA,NA,NA,NA,NA,0.2,0.18,NA,NA,NA,NA,0.94,1,NA,NA,0.94,1,NA,NA,0.03,-0.01,0.567,0.565,NA,NA,1,1,NA,NA,NA,NA,NA,NA,NA,NA
Liang et al.,2018,Impact of pre- and post-pollination barriers on pollen transfer and reproductive isolation among three sympatric Pedicularis (Orobanchaceae) species,Plant Biology,YES,NO,NO,Pedicularis,species,species,Orobanchaceae,Pedicularis comptoniifolia,Pedicularis tenuisecta,sympatric,sympatric,temperate,perennial,perennial,herb,NA,NA,NA,NA,NA,NA,NA,NA,0.04,0.04,NA,NA,NA,NA,0.72,0.89,NA,NA,0.72,0.89,NA,NA,1,0.66,1,0.94,NA,NA,1,1,NA,NA,NA,NA,NA,NA,NA,NA
Liao et al.,2019,A comparison of reproductive isolation between two closely related oak species in zones of recent and ancient secondary contact,BMC Evolutionary Biology,NO,NO,NO,Quercus,species,species,Fagaceae,Quercus mongolica,Quercus liaotungensis,sympatric,sympatric,temperate,perennial,perennial,tree,NA,NA,NA,NA,NA,NA,NA,NA,0.2,0.143,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,0.226,-0.023,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA
Lowe and Abbott,2004,"Reproductive isolation of a new hybrid species, Senecio eboracensis Abbott & Lowe (Asteraceae) ",Heredity,NO,NO,NO,Senecio,species,species,Asteraceae,Senecio eboracensis,Senecio vulgaris var. vulgaris,sympatric,sympatric,temperate,annual,annual,herb,NA,NA,NA,NA,NA,NA,NA,NA,0.584,0.643,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,0.103,0.127,NA,NA,NA,NA,0.013,0.003,0.027,-0.093,NA,NA
Lowry et al.,2008,Ecological reproductive isolation of coast and inland races of Mimulus gutattus,Evolution,NO,YES,NO,Mimulus,ecotypes,ecotypes,Phrymaceae,Mimulus guttatus (coast),Mimulus guttatus (inland),allopatric,allopatric,temperate,"perennial, annual",A / B / P,herb,NA,NA,NA,NA,NA,NA,0.995,0.779,0.979,0.953,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,0.012,0.012,0,0,0.026,0.026,NA,NA,-0.476,0.237
Ma et al.,2014,"Unidirectional hybridization and reproductive barriers between two heterostylous primrose species in northwest Yunnan, China ",Annals of Botany,NO,NO,NO,Primula,species,species,Primulaceae,Primula beesiana,Primula bulleyana,sympatric (at least some pops),sympatric,temperate,pernnial,perennial,herb,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,0,0,0,0,NA,NA,NA,NA,NA,NA,-0.103,0.303,-0.147,0.351,NA,NA,1,0.27,NA,NA,NA,NA,NA,-0.158
Ma et al.,2016,Strong reproductive isolation despite occasional hybridization between a widely distributed and a narrow endemic Rhododendron species,Nature Scientific Reports,NO,NO,NO,Rhododendron,species,species,Ericaceae,Rhododendron cyanocarpum,Rhododendron delavayi,sympatric (asymmetrical),sympatric,temperate,perennial,perennial,shrub,0,0.982,0,0.982,NA,NA,NA,NA,0.076,0.141,NA,NA,NA,NA,1,1,0.015,0.365,1,1,NA,NA,0.697,0.386,NA,NA,0.658,0.089,0.261,0.706,NA,NA,NA,NA,NA,NA,NA,NA
Marques et al.,2007,Pollination patterns limit hybridization between two sympatric species of Narcissus (Amaryllidaceae),American Journal of Botany,NO,NO,NO,Narcissus,species,species,Amaryllidaceae,Narcissus cavanillesii,Narcissus serotinus,sympatric,sympatric,temperate,perennial,perennial,herb,NA,NA,NA,NA,NA,NA,NA,NA,0.742,0.612,NA,NA,NA,NA,0.89,0.93,0.796,0.841,0.89,0.929,NA,NA,NA,NA,0.178,0.688,0.144,0.684,-0.092,0.044,NA,NA,NA,NA,NA,NA,NA,NA
Martin and Willis,2006,Ecological divergence associated with mating systemcauses nearly complete reproductive isolation between sympatric Mimulus species,Evolution,NO,YES,NO,Mimulus,species,species,Phrymaceae,Mimulus guttatus,Mimulus nasutus,sympatric,sympatric,temperate,annual,annual,herb,NA,NA,NA,NA,NA,NA,NA,NA,0.558,0.551,NA,NA,0.846,-0.846,NA,NA,NA,NA,NA,NA,NA,NA,0.892,0,NA,NA,NA,NA,0.152,-0.001,0.081,0.003,0.532,-0.517,0.512,-0.101,NA,NA
Melo et al.,2014,Strong extrinsic reproductive isolation between parapatric populations of an Australian groundsel,New Phytologist,NO,NO,NO,Senecio,ecotypes,ecotypes,Asteraceae,Senecio lautus (dune),Senecio lautus (headland),parapatric/allopatric,parapatric,temperate,perennial,perennial,herb,NA,NA,NA,NA,NA,NA,0.42,0.204,0.543,0.395,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,-0.01,-0.043,0,0,NA,NA,NA,NA,NA,NA,0.251,0.127
Miglia et al.,2005,Nine-year reciprocal transplant experiment in the gardens of the basin and mountain big sagebrush (Artemisia tridentata: Asteraceae) hybrid zone of Salt Creek Canyon: the importance of multiple-year tracking of f itness,Biological Journal of the Linnean Society,NO,YES,NO,Artemisia,ecotypes,ecotypes,Asteraceae,Artemisia tridentata (basin),Artemisia tridentata (mountain),sympatric/parapatric,parapatric,temperate,perennial,perennial,shrub,NA,NA,NA,NA,NA,NA,0.563,0.887,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,0.818,0.439
Misiewicz et al.,2020,The contribution of multiple barriers to reproduction between edaphically divergent lineages in the amazonian tree protium subserratum (Burseraceae),Ecology and Evolution,YES,NO,NO,Protium,ecotypes,ecotypes,Burseraceae,Protium subserratum (white-sand ecotype),Protium subserratum (brown-sand ecotype),parapatric (~100 meters),parapatric,tropical,perennial,perennial,tree,0.83,0.45,0.83,0.45,NA,NA,NA,NA,-0.23,0.69,NA,NA,NA,NA,0.82,0.82,0.82,0.82,NA,NA,NA,NA,NA,0.18,NA,NA,NA,0.4,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA
Murúa et al.,2017,Pollinators and crossability as reproductive isolation barriers in two sympatric oil-rewarding Calceolaria (Calceolariaceae) species,Evolutionary Ecology,NO,NO,NO,Calceolaria,species,species,Calceolariaceae,Calceolaria filicaulis,Calceolaria arachnoidea,sympatric,sympatric,temperate,perennial,perennial,herb,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,1,1,1,1,NA,NA,NA,NA,NA,NA,NA,NA,0.588,0.842,0.054,0.08,NA,NA,NA,NA,NA,NA,NA,NA
Munguia-Rosas and Jacome-Flores,2020,Reproductive isolation between wild and domesticated chaya (Cnidoscolus aconitifolius) in sympatry,Plant Biology,YES,NO,NO,Cnidoscolus,ecotypes,ecotypes,Euphorbiaceae,Cnidoscolus aconitifolius (wild),Cnidoscolus aconitifolius (domesticated),sympatric,sympatric,tropical,perennial,perennial,shrub,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,0.99,-0.99,0.77,-1,0.77,-1,NA,NA,NA,NA,0.94,NA,1,1,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA
Ostevik et al.,2016,Multiple reproductive barriers separate recently diverged sunflower ecotypes ,Evolution,YES,NO,NO,Helianthus,ecotypes,ecotypes,Asteraceae,Helianthus petiolaris (dune),Helianthus petiolaris (non-dune),parapatric,parapatric,temperate,annual,annual,herb,NA,NA,NA,NA,NA,NA,0.89,0.76,0.093,0.093,NA,NA,NA,NA,0.55,0.36,0.55,0.36,NA,NA,NA,NA,0.38,0.12,NA,NA,NA,NA,0.003,0.006,NA,NA,0.01,-0.03,NA,NA,0.785,0.68
Paudel et al.,2018,Reproductive isolation in alpine gingers: how do co-existing Roscoea (R. purpurea and R. tumjensis) conserve species integrity?,Evolution,YES,NO,NO,Roscoea,species,species,Zingiberaceae,Roscoea purpurea,Roscoea tumjensis,sympatric,sympatric,temperate,perennial,perennial,herb,0.947,0.198,0.947,0,0.254,0.198,NA,NA,0.983,0.99,NA,NA,NA,NA,1,1,NA,NA,1,1,NA,NA,NA,NA,0.025,0.018,0.066,0.018,0.03,-0.073,NA,NA,NA,NA,NA,NA,NA,NA
Pegoraro et al.,2016,Habitat preference and flowering‐time variation contribute to reproductive isolation between diploid and autotetraploid Anacamptis pyramidalis,Journal of Evolutionary Biology,YES,NO,YES,Anacamptis,cytotypes,cytotypes,Orchidaceae,Anacamptis pyramidalis (diploid),Anacamptis pyramidalis (tetraploid),sympatric,sympatric,temperate,perennial,perennial,herb,0.72,NA,NA,NA,0.72,NA,NA,NA,0.663,NA,NA,NA,NA,NA,0,NA,NA,NA,NA,NA,0,NA,0,NA,NA,NA,0.12,NA,NA,NA,NA,NA,0.982,NA,NA,NA,0.085,NA
Pellegrino et al.,2010,"Strong post-pollination pre-zygotic isolation between sympatric, food-deceptive Mediterranean orchids",Sexual Plant Reproduction,NO,NO,NO,Orchis,species,species,Orchidaceae,Orchis italica,Orchis papilionacea,sympatric,sympatric,temperate,perennial,perennial,herb,NA,NA,NA,NA,NA,NA,NA,NA,0.333,0.364,NA,NA,NA,NA,0.125,0.462,0.125,0.462,NA,NA,NA,NA,NA,NA,1,1,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA
Ramírez‐Aguirre et al.,2019,Reproductive isolation among three sympatric Achimenes species: pre‐ and post‐pollination components,American Journal of Botany,YES,NO,NO,Achimenes,species,species,Gesneriaceae,Achimenes antirrhina,Achimenes flava,sympatric,sympatric,tropical,perennial,perennial,herb,0.638,0.638,0.638,0.638,NA,NA,NA,NA,0.83,0.708,NA,NA,NA,NA,1,1,1,1,NA,NA,NA,NA,NA,NA,0.66,0.7,NA,0,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA
Ramírez‐Aguirre et al.,2019,Reproductive isolation among three sympatric Achimenes species: pre‐ and post‐pollination components,American Journal of Botany,YES,NO,NO,Achimenes,species,species,Gesneriaceae,Achimenes antirrhina,Achimenes patens,sympatric,sympatric,tropical,perennial,perennial,herb,0.743,0.743,0.743,0.743,NA,NA,NA,NA,0.305,0.261,NA,NA,NA,NA,1,1,1,1,NA,NA,NA,NA,NA,NA,0.56,0.21,NA,0.5,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA
Ramírez‐Aguirre et al.,2019,Reproductive isolation among three sympatric Achimenes species: pre‐ and post‐pollination components,American Journal of Botany,YES,NO,NO,Achimenes,species,species,Gesneriaceae,Achimenes flava,Achimenes patens,sympatric,sympatric,tropical,perennial,perennial,herb,0.716,0.715,0.716,0.715,NA,NA,NA,NA,0.432,0.494,NA,NA,NA,NA,1,0.8,1,0.8,NA,NA,NA,NA,NA,NA,-0.006,0.089,0.35,0.292,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA
Ramsey et al.,2003,Components of reproductive isolation between the monkeyflowers Mimulus lewisii and M. cardinalis (Phrymaceae),Evolution,NO,YES,NO,Mimulus,species,species,Phrymaceae,Mimulus lewisii,Mimulus cardinalis,sympatric,sympatric,temperate,perennial,perennial,herb,0.32,0.1,0.32,0.1,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,0.952,0.952,NA,NA,0.952,0.952,NA,NA,0.226,0.88,NA,NA,0.254,0.33,0.113,0.024,0,0.029,0.495,0.458,0.257,0.584,NA,NA
Richards and Ortiz-Barrientos,2016,Immigrant inviability produces a strong barrier to gene flow between parapatric ecotypes of Senecio lautus,Evolution,YES,NO,NO,Senecio,ecotypes,ecotypes,Asteraceae,Senecio lautus (dune),Senecio lautus (headland),parapatric,parapatric,temperate,perennial,perennial,herb,NA,NA,NA,NA,NA,NA,0.786,1,-0.585,0.59,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,-0.139,-0.125,-0.123,-0.153,NA,NA,NA,NA,0.251,0.952
Richards and Ortiz-Barrientos,2016,Immigrant inviability produces a strong barrier to gene flow between parapatric ecotypes of Senecio lautus,Evolution,YES,NO,NO,Senecio,ecotypes,ecotypes,Asteraceae,Senecio lautus (dune),Senecio lautus (island),parapatric,parapatric,temperate,perennial,perennial,herb,NA,NA,NA,NA,NA,NA,1,1,-0.465,0.467,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,0.346,-0.719,0.131,-0.2,NA,NA,NA,NA,0.707,0.306
Richards and Ortiz-Barrientos,2016,Immigrant inviability produces a strong barrier to gene flow between parapatric ecotypes of Senecio lautus,Evolution,YES,NO,NO,Senecio,ecotypes,ecotypes,Asteraceae,Senecio lautus (headland),Senecio lautus (island),parapatric,parapatric,temperate,perennial,perennial,herb,NA,NA,NA,NA,NA,NA,0.993,0.741,0.135,0.1,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,0.026,-0.842,0.133,-0.169,NA,NA,NA,NA,1,1
Roccaforte et al.,2015,Hybridization and reproductive isolation between diploid Erythronium mesochoreum and its tetraploid congener E. albidum (Liliaceae) ,Evolution,YES,NO,YES,Erythronium,cytotypes,cytotypes,Liliaceae,Erythronium albidum (tetraploid),Erythronium mesochoreum (diploid),sympatric,sympatric,temperate,perennial,perennial,herb,0.875,0.7,0.875,0.7,NA,NA,NA,NA,0.174,0.228,NA,NA,NA,NA,0.41,0.767,0.41,0.767,NA,NA,NA,NA,NA,NA,NA,NA,0.285,0.236,NA,NA,NA,NA,0.81,0.89,NA,NA,NA,NA
Sambatti et al.,2012,Reconciling extremely strong barriers with high levels of gene exchange in annual sunflowers,Evolution,NO,NO,NO,Helianthus,species,species,Asteraceae,Helianthus annuus,Helianthus petiolaris,NA,NA,temperate,annual,annual,herb,0.81,0.775,0.81,0.775,NA,NA,0.587,-0.345,0.14,0.1,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,0.942,0.992,NA,NA,-0.011,-0.01,0.061,0.031,NA,NA,0.905,0.904,0.982,0.995,NA,NA
Sedeek et al.,2014,Genic rather than genome-wide differences between sexually deceptive Ophyrys orchids with different pollinators,Molecular Ecology,NO,NO,NO,Ophrys,species,species,Orchidaceae,Ophrys incubacea,Ophrys exaltata,sympatric,sympatric,temperate,perennial,perennial,herb,NA,NA,NA,NA,NA,NA,NA,NA,0.33,0.33,NA,NA,NA,NA,1,NA,NA,NA,NA,NA,1,NA,NA,NA,NA,0.2,NA,-0.158,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA
Sedeek et al.,2014,Genic rather than genome-wide differences between sexually deceptive Ophyrys orchids with different pollinators,Molecular Ecology,NO,NO,NO,Ophrys,species,species,Orchidaceae,Ophrys incubacea,Ophrys garganica,sympatric,sympatric,temperate,perennial,perennial,herb,NA,NA,NA,NA,NA,NA,NA,NA,0.06,0.06,NA,NA,NA,NA,1,0.846,NA,NA,NA,NA,1,0.846,NA,NA,NA,0.167,NA,-0.152,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA
Sedeek et al.,2014,Genic rather than genome-wide differences between sexually deceptive Ophyrys orchids with different pollinators,Molecular Ecology,NO,NO,NO,Ophrys,species,species,Orchidaceae,Ophrys incubacea,Ophrys sphegodes,sympatric,sympatric,temperate,perennial,perennial,herb,NA,NA,NA,NA,NA,NA,NA,NA,0.49,0.49,NA,NA,NA,NA,1,1,NA,NA,NA,NA,1,1,NA,NA,NA,-0.072,NA,-0.345,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA
Sobel and Streisfeld,2014,Strong premating reproductive isolation drives incipient speciation in Mimulus aurantiacus,Evolution,YES,NO,NO,Mimulus,ecotypes,ecotypes,Phrymaceae,Mimulus aurantiacus (red),Mimulus aurantiacus (yellow),parapatric (small hybrid zone),parapatric,temperate,perennial,perennial,shrub,0.777,0.786,0.777,0.786,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,0.873,0.647,NA,NA,0.873,0.647,NA,NA,0.125,-0.072,NA,NA,-0.044,0.008,-0.062,0.032,0.004,-0.005,0.017,0.023,NA,NA,NA,NA
Stanton et al.,2016,Absence of postmating barriers between a selfing vs. outcrossing Chilean Mimulus species pair,American Journal of Botany,NO,NO,NO,Mimulus,species,species,Phrymaceae,Mimulus luteus,Mimulus cupreus,sympatric,sympatric,temperate,perennial,perennial,herb,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,-0.263,0.391,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,0.274,0.034,-0.009,0.005,-0.319,0,NA,NA,-0.183,0.599,NA,NA
Sun et al.,2015,Floral isolation is the major reproductive barrier between a pair of rewarding orchid sister species,Journal of Evolutionary Biology,NO,NO,NO,Gymnadenia,species,species,Orchidaceae,Gymnadenia conopsea,Gymnadenia odoratissima,sympatric,sympatric,temperate,perennial,perennial,herb,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,1,1,NA,NA,1,1,NA,NA,NA,NA,-0.029,0.068,0.079,0.005,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA
Tao et al.,2018,Does reproductive isolation reflect the segregation of color forms in Spiranthes sinensis (Pers.) Ames complex (Orchidaceae) in the Chinese Himalayas?,Ecology and Evolution,YES,NO,NO,Spiranthes,ecotypes,ecotypes,Orchidaceae,Spiranthes sinensis (pink),Spiranthes sinensis (white),sympatric,sympatric,temperate,perennial,perennial,herb,NA,NA,NA,NA,NA,NA,NA,NA,0.11,0.15,NA,NA,NA,NA,0.52,0.88,NA,NA,0.52,0.88,NA,NA,-0.03,0.09,0.39,0.06,0.23,0.02,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA
Tong and Huang,2016,Pre- and post-pollination interaction between six co-flowering Pedicularis species via heterospecific pollen transfer,New Phytologist,NO,NO,NO,Pedicularis,species,species,Orobanchaceae,Pedicularis longiflora,Pedicularis cephalantha,sympatric,sympatric,temperate,perennial,perennial,herb,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,0.988,0.995,NA,NA,0.988,0.995,0.895,0.995,1,1,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA
Tong and Huang,2016,Pre- and post-pollination interaction between six co-flowering Pedicularis species via heterospecific pollen transfer,New Phytologist,NO,NO,NO,Pedicularis,species,species,Orobanchaceae,Pedicularis siphonantha,Pedicularis densispica,sympatric,sympatric,temperate,perennial,perennial,herb,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,0.962,0.999,NA,NA,0.962,0.999,0.71,0.997,1,0.167,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA
Tong and Huang,2016,Pre- and post-pollination interaction between six co-flowering Pedicularis species via heterospecific pollen transfer,New Phytologist,NO,NO,NO,Pedicularis,species,species,Orobanchaceae,Pedicularis cephalantha,Pedicularis densispica,sympatric,sympatric,temperate,perennial,perennial,herb,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,0.945,1,NA,NA,0.945,0.99,0.917,1,1,0.052,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA
Tong and Huang,2016,Pre- and post-pollination interaction between six co-flowering Pedicularis species via heterospecific pollen transfer,New Phytologist,NO,NO,NO,Pedicularis,species,species,Orobanchaceae,Pedicularis tricolor,Pedicularis confertiflora,sympatric,sympatric,temperate,perennial,perennial,herb,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,0.924,0.943,NA,NA,0.772,0.909,0.924,0.943,1,0.624,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA
Volis et al.,2019,Divergence and reproductive isolation between two closely related allopatric Iris species,Biological Journal of the Linnean Society,YES,NO,NO,Iris,species,species,Iridaceae,Iris atrofusca,Iris mariae,allopatric,allopatric,temperate,perennial,perennial,herb,0.95,0.921,0.95,0.921,NA,NA,-0.026,0.289,0.237,0.256,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,-0.268,0.014,-0.107,-0.024,NA,NA,NA,NA,NA,NA,NA,NA
Wang et al.,1997,Narrow hybrid zone between two subspecies of big Sagebrush (Artemsia tridentata: Asteraceae). IV. Reciprocal transplant experiments.,Evolution,NO,NO,NO,Artemisia,ecotypes,ecotypes,Asteraceae,Artemisia tridentata (basin),Artemisia tridentata (mountain),sympatric,parapatric,temperate,perennial,perennial,shrub,NA,NA,NA,NA,NA,NA,0.802,0.869,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,0.869,0.266
Wang et al.,2015,Reproductive isolation is mediated by pollen incompatibility in sympatric populations of two Arnebia species,Ecology and Evolution,NO,NO,NO,Arnebia,species,species,Boraginaceae,Arnebia guttata,Arnebia szechenyi,sympatric,sympatric,temperate,perennial,perennial,herb,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,-0.42,0.62,NA,NA,-0.42,0.62,NA,NA,1,1,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA
Whitehead and Peakall,2014,Pollinator specificty drives strong prepollination reproductive isolation in sympatric sexually deceptive orchids,Evolution,NO,NO,NO,Chiloglottis,species,species,Orchidaceae,Chiloglottis valida,Chiloglottis aff jeanesii (undescribed),sympatric,sympatric,temperate,perennial,perennial,herb,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA,1,1,NA,NA,1,1,NA,NA,NA,NA,-0.085,-0.058,-0.073,-0.026,NA,NA,-0.333,-0.717,NA,NA,NA,NA,NA,NA
Xie et al.,2017,Natural hybridization and reproductive isolation between two Primula species,Journal of Integrative Plant Biology,NO,NO,NO,Primula,species,species,Primulaceae,Primula secundiflora,Primula poissonii,sympatric,sympatric,temperate,perennial,perennial,herb,NA,NA,NA,NA,NA,NA,NA,NA,0.111,0.13,NA,NA,NA,NA,0,0.208,0,0.208,-0.259,-0.169,NA,NA,NA,NA,NA,NA,0.957,0.451,NA,NA,NA,NA,NA,NA,NA,NA,NA,NA
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