Global mapped Stabilization factor (STBI)
Authors/Creators
Description
Global map of modeled initial decomposition rates as described in Sarneel et al., (xxxx) Reading tea leaves worldwide: decoupled drivers of initial litter decomposition mass-loss rate and stabilization. Ecology letters
META INFORMATION
TBI_S-xxx.tiff are separate pieces of the maps. all maps are tiled and contain 8 bands (starting with “S”), they are orderd according the list below:
S_Ensemble_mean > prediction mean from 10 ensemble models
S_Bootstrapped_mean > bootstrapped mean from 100 bootstrap samples, using best performing model from cross-validation
S_Bootstrapped_lower > lower 2.5% confidence interval from 100 bootstrap samples
S_Bootstrapped_upper > upper 97.5% confidence interval from 100 bootstrap samples
S_Bootstrapped_stdDev > standard deviation from 100 bootstrap samples
S_Bootstrapped_coefOfVar > coefficient of variation (std dev / mean) from 100 bootstrap samples
univariate_pct_int_ext > proportion of interpolation in univariate space
PCA_pct_int_ext > proportion of interpolation in bivariate combinations for PCA-transformed axes- feature importances
Other (English)
if (!require("pacman")) install.packages("pacman")
pacman::p_load(raster,mapplots,rgdal,tidyverse)
mapdata<-"C:/..."
#read a specific band from the files (in the case below band 2; bootstrapped mean)
S1<-raster(("C:/.../TBI_S-0000000000-0000000000.tif"), band = 2) %>% aggregate(fact=20)
S2<-raster(("C:/.../TBI_S-0000000000-0000011776.tif"), band = 2) %>% aggregate(fact=20)
S3<-raster(("C:/.../TBI_S-0000000000-0000023552.tif"), band = 2) %>% aggregate(fact=20)
S4<-raster(("C:/.../TBI_S-0000000000-0000035328.tif"), band = 2) %>% aggregate(fact=20)
S5<-raster(("C:/.../TBI_S-0000011776-0000000000.tif"), band = 2) %>% aggregate(fact=20)
S6<-raster(("C:/.../TBI_S-0000011776-0000011776.tif"), band = 2) %>% aggregate(fact=20)
S7<-raster(("C:/.../TBI_S-0000011776-0000023552.tif"), band = 2) %>% aggregate(fact=20)
S8<-raster(("C:/.../TBI_S-0000011776-0000035328.tif"), band = 2) %>% aggregate(fact=20)
#glue them together
S_all<-mosaic(S8,S7,S6,S5,S4,S3,S2,S1,tolerance=1,fun=mean)
#plot the map
plot(S_all, col=colorRampPalette(c( "aquamarine","mediumaquamarine", "palegreen4","darkslategrey","black"))( 11 ),breaks = c(0,0.1,0.15,0.2,0.25,0.3,0.35,0.4,0.45,0.5,0.6,0.8),
legend=F, axes=FALSE,xlim=c(-200,200),ylim=c(-60,100))
ticks<- c(0, 0.2, 0.4,0.6, 0.8)
plot(S_all, legend.only=TRUE, col=colorRampPalette(c( "aquamarine","mediumaquamarine", "palegreen4","darkslategrey","black"))( 11 ),breaks = c(0,0.1,0.15,0.2,0.25,0.3,0.35,0.4,0.45,0.5,0.6,0.8),
legend.width=1, axis.args=list( at=ticks, labels=ticks), legend.shrink=0.7,legend.args=list(text='STBI', side=3, font=2, line=0.2, cex=1),
smallplot=c(0.07,0.10, 0.15,0.50)); par(mar = par("mar"))
#DONE
Methods (English)
Geospatial modelling
To explore spatial patterns of early mass-loss dynamics of plant litter and derive global maps of predicted TBI proxies, separate random forest models were built for STBI and ln-transformed k1TBI, following the procedure outlined in van den Hoogen et al. (2019). We performed a grid search procedure to tune the random forest models across a range of 30 hyper-parameter settings (with 2–10 variables per split and 2–6 as a minimum leaf population). For each of the 30 models, we assessed the model performance using k-fold cross-validation (using k=10; folds assigned randomly, stratified per biome to ensure equal representation of each bioclimatic zone). The mean coefficient of determination R2 across the tested models was the basis for choosing the best model (van den Hoogen et al. 2019). The final image was subsequently calculated as a mean of the top 10 best performing hyperparameter settings. To generate coefficients of variation images (standard deviation divided by mean) that provides a per-pixel accuracy of our predicted TBI, we followed a stratified bootstrapping procedure (stratified per biome). After classifying the composite raster data 100 times, we used these to create per-pixel mean and standard deviation images. The resulting maps of predicted TBI proxies and associated models should be used to address large rather than small spatial scales.
To quantify the potential extrapolation of our TBI maps we assessed if the pixels with measurements covered the environmental conditions of the pixels without measurements, taking into account combinations of two environmental variables. To this end, we first performed a PCA using the 125 covariate layers for all pixels for which we had measurements (van den Hoogen et al. 2019). Second, we transformed all terrestrial pixels without measurements into the same PCA space by using scaling and centring the eigenvectors and values of the PCA. Third, we represented the sampled environmental conditions (interpolation) by creating PCA convex hulls enclosing the pixels with measurements. We did this for all bivariate combinations of the first 28 PCA axes (explaining >90% of the PCA-variation and resulting in 378 combinations). Last, for each pixel without measurements, we quantified a per-pixel degree of interpolation as the % of the convex hulls that included this pixel. Geospatial analyses and extrapolation were performed in Google Earth Engine and Python
Files
TBI_S-map.zip
Files
(5.0 GB)
| Name | Size | Download all |
|---|---|---|
|
md5:2de7ba096b5d6714b94501d80d1712c2
|
5.0 GB | Preview Download |
Additional details
Related works
- Is derived from
- Dataset: 10.5281/zenodo.10514225 (DOI)
- Is supplemented by
- Image: 10.5281/zenodo.10513802 (DOI)
Funding
- Swedish Research Council
- Teatime4science 2014-04270
- Swedish Research Council
- TeaTales 2021-02449
References
- van den Hoogen et al. (2019). 1. Austin, A.T. & Vivanco, L. (2006). Plant litter decomposition in a semi-arid ecosystem controlled by photodegradation. Nature, 442, 555-558. 2. Bardgett, R.D. & van der Putten, W.H. (2014). Belowground biodiversity and ecosystem functioning. Nature, 515, 505-511. 3. Berg, B., Berg, M.P., Bottner, P., Box, E., Breymeyer, A., Deanta, R.C. et al. (1993). Litter mass-loss rates in pine forests of europe and eastern united-states - some relationships with climate and litter quality. Biogeochemistry, 20, 127-159. 4. Berg, B. & McClaugherty, C. (2020). Plant Litter; Decomposition, Humus formation, Carbon sequestration. 4th edition edn. Springer, New York, USA. 5. Buckeridge, K.M., Mason, K.E., McNamara, N.P., Ostle, N., Puissant, J., Goodall, T. et al. (2020). Environmental and microbial controls on microbial necromass recycling, an important precursor for soil carbon stabilization. Communications Earth & Environment, 1. 6. Cebrian, J. (1999). Patterns in the fate of production in plant communities. Am. Nat., 154, 449-468. 7. Cotrufo, M.F., Soong, J.L., Horton, A.J., Campbell, E.E., Haddix, M.L., Wall, D.H. et al. (2015). Formation of soil organic matter via biochemical and physical pathways of litter mass loss. Nature Geoscience, 8, 776-+. 8. Cotrufo, M.F., Wallenstein, M.D., Boot, C.M., Denef, K. & Paul, E. (2013). The Microbial Efficiency-Matrix Stabilization (MEMS) framework integrates plant litter decomposition with soil organic matter stabilization: do labile plant inputs form stable soil organic matter? Global Change Biol., 19, 988-995. 9. Djukic, I., Kepfer-Rojas, S., Schmidt, I.K., Larsen, K.S., Beier, C., Berg, B. et al. (2018). Early stage litter decomposition across biomes. Sci. Total Environ., 628-629, 1369-1394. 10. Duddigan, S., Alexander, P.D., Shaw, L.J., Sanden, T. & Collins, C.D. (2020a). The Tea Bag Index-UK: Using Citizen/Community Science to Investigate Organic Matter Decomposition Rates in Domestic Gardens. Sustainability, 12. 11. Duddigan, S., Shaw, L.J., Alexander, P.D. & Collins, C.D. (2020b). Chemical Underpinning of the Tea Bag Index: An Examination of the Decomposition of Tea Leaves. Applied and Environmental Soil Science, 2020. 12. Fanin, N., Bezaud, S., Sarneel, J.M., Cecchini, S., Nicolas, M. & Augusto, L. (2020). Relative Importance of Climate, Soil and Plant Functional Traits During the Early Decomposition Stage of Standardized Litter. Ecosystems, 23, 1004-1018. 13. Foley, J.A. (2005). Integrated Biosphere Simulator Model (IBIS), Version 2.5. Available at: https://daac.ornl.gov/cgi-bin/dsviewer.pl?ds_id=8082020. 14. Gessner, M.O., Chauvet, E. & Dobson, M. (1999). A perspective on leaf litter breakdown in streams. Oikos, 85, 377-384. 15. Gholz, H.L., Wedin, D.A., Smitherman, S.M., Harmon, M.E. & Parton, W.J. (2000). Long-term dynamics of pine and hardwood litter in contrasting environments: toward a global model of decomposition. Global Change Biol., 6, 751-765. 16. Gorelick, N., Hancher, M., Dixon, M., Ilyushchenko, S., Thau, D. & Moore, R. (2017). Google Earth Engine: Planetary-scale geospatial analysis for everyone. Remote Sens. Environ., 202, 18-27. 17. Harmon, M.E. (2016). LTER Intersite Fine Litter Decomposition Experiment (LIDET), 1990 to 2002 version 11. (ed. Site, AFL) Corvallis. 18. He, Y., Wang, X.H., Wang, K., Tang, S.C., Xu, H., Chen, A.P. et al. (2021). Data-driven estimates of global litter production imply slower vegetation carbon turnover. Global Change Biol., 27, 1678-1688. 19. Heimann, M. & Reichstein, M. (2008). Terrestrial ecosystem carbon dynamics and climate feedbacks. Nature, 451, 289-292. 20. Hobbie, S.E., Eddy, W.C., Buyarski, C.R., Adair, E.C., Ogdahl, M.L. & Weisenhorn, P. (2012). Response of decomposing litter and its microbial community to multiple forms of nitrogen enrichment. Ecol. Monogr., 82, 389-405. 21. IPCC (2022). Climate Change 2022: Impacts, Adaptation, and Vulnerability. Contribution of Working Group II to the Sixth Assessment Report of the Intergovernmental Panel on Climate Change. (eds. Pörtner, H-O, Roberts, DC, Tignor, M, Poloczanska, ES, Mintenbeck, K, Alegría, A et al.) Cambridge, UK and New York, USA, p. 3056. 22. Joly, F.X., Scherer-Lorenzen, M. & Hättenschwiler, S. (2023). Resolving the intricate role of climate in litter decomposition. Nature Ecology & Evolution. 23. Keuskamp, J.A., Dingemans, B.J.J., Lehtinen, T., Sarneel, J.M. & Hefting, M.M. (2013). Tea Bag Index: a novel approach to collect uniform decomposition data across ecosystems. Methods in Ecology and Evolution, 4, 1070-1075. 24. Kwon, T., Shibata, H., Kepfer-Rojas, S., Schmidt, I.K., Larsen, K.S., Beier, C. et al. (2021). Effects of Climate and Atmospheric Nitrogen Deposition on Early to Mid-Term Stage Litter Decomposition Across Biomes. Frontiers in Forests and Global Change, 4. 25. Le Noë, J., Manzoni, S., Abramoff, R., Bölscher, T., Bruni, E., Cardinael, R. et al. (2023). Soil organic carbon models need independent time-series validation for reliable prediction. Communications Earth & Environment, 4. 26. Lenth, R.V., Bolker, B., Buerkner, P., Gine-Vasquez, I., Herve, M., Jung, M. et al. (2023). Emmeans: Estimated Marginal Means, aka Least-Squares Means. 27. Li, R.S., Guo, X.Y., Han, J.M., Yang, Q.P., Zhang, W.D., Yu, X. et al. (2023). Global pattern and drivers of stable residue size from decomposing leaf litter. Catena, 232. 28. Minasny, B., Malone, B.P., McBratney, A.B., Angers, D.A., Arrouays, D., Chambers, A. et al. (2017). Soil carbon 4 per mille. Geoderma, 292, 59-86. 29. Mori, T., Nakamura, R. & Aoyagi, R. (2022). Risk of misinterpreting the Tea Bag Index: Field observations and a random simulation. Ecol. Res., 37, 381-389. 30. Mueller, P., Schile-Beers, L.M., Mozdzer, T.J., Chmura, G.L., Dinter, T., Kuzyakov, Y. et al. (2018). Global-change effects on early-stage decomposition processes in tidal wetlands - implications from a global survey using standardized litter. Biogeosciences, 15, 3189-3202. 31. Njoroge, D.M., Chen, S.C., Zuo, J., Dossa, G.G.O. & Cornelissen, J.H.C. (2022). Soil fauna accelerate litter mixture decomposition globally, especially in dry environments. J. Ecol., 110, 659-672. 32. Ochoa-Hueso, R., Borer, E.T., Seabloom, E.W., Hobbie, S.E., Risch, A.C., Collins, S.L. et al. (2020). Microbial processing of plant remains is co-limited by multiple nutrients in global grasslands. Global Change Biol., 26, 4572-4582. 33. Olson, D.M., Dinerstein, E., Wikramanayake, E.D., Burgess, N.D., Powell, G.V.N., Underwood, E.C. et al. (2001). Terrestrial ecoregions of the worlds: A new map of life on Earth. Bioscience, 51, 933-938. 34. Parton, W., Silver, W.L., Burke, I.C., Grassens, L., Harmon, M.E., Currie, W.S. et al. (2007). Global-scale similarities in nitrogen release patterns during long-term decomposition. Science, 315, 361-364. 35. Parton, W.J., Hartman, M., Ojima, D. & Schimel, D. (1998). DAYCENT and its land surface submodel: description and testing. Global Planet. Change, 19, 35-48. 36. Post, E., Alley, R.B., Christensen, T.R., Macias-Fauria, M., Forbes, B.C., Gooseff, M.N. et al. (2019). The polar regions in a 2 degrees C warmer world. Science Advances, 5. 37. Prescott, C.E. (2010). Litter decomposition: what controls it and how can we alter it to sequester more carbon in forest soils? Biogeochemistry, 101, 133-149. 38. R Core Team (2023). R: A language and environment for statistical computing. R Foundation for Statistical Computing Vienna, Austria. 39. Robbins, C.J., Norman, B.C., Halvorson, H.M., Manning, D.W., Bastias, E., Biasi, C. et al. (2022). Nutrient and stoichiometric time series measurements of decomposing coarse detritus in freshwaters worldwide from literature published between 1976-2020 ver 1. (ed. Initiative, ED). 40. Sanchez, P.A., Ahamed, S., Carre, F., Hartemink, A.E., Hempel, J., Huising, J. et al. (2009). Digital soil map of the world. Science, 325, 680-681. 41. Sarneel, J.M., Barel, J.M., Duddigan, S., Keuskamp, J.A., Pastor Oliveras, A., Sanden, T. et al. (2023). Reasons to not correct for leaching in TBI; reply to Lind et al 2022. Authorea. 42. Sarneel, J.M.J. & Veen, G.F.C. (2017). Legacy effects of altered flooding regimes on decomposition in a boreal floodplain. Plant Soil, 421, 57-66. 43. Stockmann, U., Padarian, J., McBratney, A., Minasny, B., de Brogniez, D., Montanarella, L. et al. (2015). Global soil organic carbon assessment. Global Food Security-Agriculture Policy Economics and Environment, 6, 9-16. 44. Tang, H., Nolte, S., Jensen, K., Yang, Z., Wu, J. & Mueller, P. (2020). Grazing mediates soil microbial activity and litter decomposition in salt marshes. Sci. Total Environ., 720. 45. Thomas, H.J.D., Myers-Smith, I.H., Høye, T.T., Bon, M.P., Lembrechts, J., Walker, E.R. et al. (2023). Litter quality outweighs climate as a driver of decomposition across the tundra biome. EcoEvoRxiv. 46. Trofymow, J.A., Moore, T.R., Titus, B., Prescott, C., Morrison, I., Siltanen, M. et al. (2002). Rates of litter decomposition over 6 years in Canadian forests: influence of litter quality and climate. Canadian Journal of Forest Research-Revue Canadienne De Recherche Forestiere, 32, 789-804. 47. van den Brink, L., Canessa, R., Neidhardt, H., Knuver, T., Rios, R.S., Saldana, A. et al. (2023). No home-field advantage in litter decomposition from the desert to temperate forest. Funct. Ecol., 37, 1315-1327. 48. van den Hoogen, J., Geisen, S., Routh, D., Ferris, H., Traunspurger, W., Wardle, D.A. et al. (2019). Soil nematode abundance and functional group composition at a global scale. Nature, 572, 194-+.
- Keuskamp et al., (2013). Tea Bag Index: a novel approach to collect uniform decomposition data across ecosystems. Methods in Ecology and Evolution, 4, 1070-1075.