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The global distribution and environmental drivers of aboveground versus belowground plant biomass

Abstract

A poor understanding of the fraction of global plant biomass occurring belowground as roots limits our understanding of present and future ecosystem function and carbon pools. Here we create a database of root-mass fractions (RMFs), an index of plant below- versus aboveground biomass distributions, and generate quantitative, spatially explicit global maps of RMFs in trees, shrubs and grasses. Our analyses reveal large gradients in RMFs both across and within vegetation types that can be attributed to resource availability. High RMFs occur in cold and dry ecosystems, while low RMFs dominate in warm and wet regions. Across all vegetation types, the directional effect of temperature on RMFs depends on water availability, suggesting feedbacks between heat, water and nutrient supply. By integrating our RMF maps with existing aboveground plant biomass information, we estimate that in forests, shrublands and grasslands, respectively, 22%, 47% and 67% of plant biomass exists belowground, with a total global belowground fraction of 24% (20–28%), that is, 113 (90–135) Gt carbon. By documenting the environmental correlates of root biomass allocation, our results can inform model projections of global vegetation dynamics under current and future climate scenarios.

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Fig. 1: RMF sample locations in forests, shrublands and grasslands.
Fig. 2: RMF variation and model validation.
Fig. 3: The global distribution of RMFs in forests, grasslands and shrublands.
Fig. 4: Relationships between environmental variables and RMFs.
Fig. 5: Spatial variations in the environmental correlates of RMFs.
Fig. 6: The global distribution of belowground plant biomass.

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Data availability

The root–shoot ratio data underlying this study are available at https://github.com/haozhima95/Global_mapping_root_shoot_ratio/tree/master/RSR_data. Citations for the root–shoot ratio data are provided in the methods.

Code availability

The code used for this study is available at https://github.com/haozhima95/Global_mapping_root_shoot_ratio.git.

References

  1. Erb, K. H. et al. Unexpectedly large impact of forest management and grazing on global vegetation biomass. Nature 553, 73–76 (2018).

    Article  CAS  PubMed  Google Scholar 

  2. Luyssaert, S. et al. Old-growth forests as global carbon sinks. Nature 455, 213–215 (2008).

    Article  CAS  PubMed  Google Scholar 

  3. Drake, J. B. et al. Above-ground biomass estimation in closed canopy Neotropical forests using lidar remote sensing: factors affecting the generality of relationships. Glob. Ecol. Biogeogr. 12, 147–159 (2003).

    Article  Google Scholar 

  4. Lefsky, M. A. et al. Lidar remote sensing of above-ground biomass in three biomes. Glob. Ecol. Biogeogr. 11, 393–399 (2002).

    Article  Google Scholar 

  5. Duncanson, L. et al. The importance of consistent global forest aboveground biomass product validation. Surv. Geophys. 40, 979–999 (2019).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  6. Spawn, S. A., Sullivan, C. C., Lark, T. J. & Gibbs, H. K. Harmonized global maps of above and belowground biomass carbon density in the year 2010. Sci. Data 7, 112 (2020).

    Article  PubMed  PubMed Central  Google Scholar 

  7. Ottaviani, G. et al. The neglected belowground dimension of plant dominance. Trends Ecol. Evol. 35, 763–766 (2020).

    Article  PubMed  Google Scholar 

  8. Jackson, L. E., Burger, M. & Cavagnaro, T. R. Roots, nitrogen transformations, and ecosystem services. Annu. Rev. Plant Biol. 59, 341–363 (2008).

    Article  CAS  PubMed  Google Scholar 

  9. Gill, R. A. & Jackson, R. B. Global patterns of root turnover for terrestrial ecosystems. New Phytol. 147, 13–31 (2000).

    Article  Google Scholar 

  10. Robinson, D. Implications of a large global root biomass for carbon sink estimates and for soil carbon dynamics. Proc. R. Soc. Lond. B 274, 2753–2759 (2007).

    CAS  Google Scholar 

  11. Bardgett, R. D., Mommer, L. & De Vries, F. T. Going underground: root traits as drivers of ecosystem processes. Trends Ecol. Evol. 29, 692–699 (2014).

    Article  PubMed  Google Scholar 

  12. Ribeiro, S. C. et al. Above- and belowground biomass in a Brazilian Cerrado. For. Ecol. Manage. 262, 491–499 (2011).

    Article  Google Scholar 

  13. Mokany, K., Raison, R. J. & Prokushkin, A. S. Critical analysis of root:shoot ratios in terrestrial biomes. Glob. Chang. Biol. 12, 84–96 (2006).

    Article  Google Scholar 

  14. Saatchi, S. S. et al. Benchmark map of forest carbon stocks in tropical regions across three continents. Proc. Natl Acad. Sci. USA 108, 9899–9904 (2011).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  15. Ruesch, A. S. & Gibbs, H. H. K. New IPCC Tier-1 Global Biomass Carbon Map for the Year 2000 (Carbon Dioxide Information Analysis Center, Oak Ridge National Laboratory, 2008).

  16. Chen, J. L. & Reynolds, J. F. A coordination model of whole-plant carbon allocation in relation to water stress. Ann. Bot. 80, 45–55 (1997).

    Article  CAS  Google Scholar 

  17. Franklin, O. et al. Modeling carbon allocation in trees: a search for principles. Tree Physiol. 32, 648–666 (2012).

    Article  CAS  PubMed  Google Scholar 

  18. Bloom, A. J., Chapin, F. S. & Mooney, H. A. Resource limitation in plants—an economic analogy. Annu. Rev. Ecol. Syst. 16, 363–392 (1985).

    Article  Google Scholar 

  19. Poorter, H. et al. Biomass allocation to leaves, stems and roots: meta-analyses of interspecific variation and environmental control. New Phytol. 193, 30–50 (2012).

    Article  CAS  PubMed  Google Scholar 

  20. Reich, P. in Plant Roots: The Hidden Half (eds. Waisel, Y. et al.) 205–220 (Marcel Dekker, 2006).

  21. Ledo, A. et al. Tree size and climatic water deficit control root to shoot ratio in individual trees globally. New Phytol. 217, 8–11 (2018).

    Article  PubMed  Google Scholar 

  22. Qi, Y., Wei, W., Chen, C. & Chen, L. Plant root-shoot biomass allocation over diverse biomes: a global synthesis. Glob. Ecol. Conserv. 18, e00606 (2019).

    Article  Google Scholar 

  23. Reich, P. B. et al. Temperature drives global patterns in forest biomass distribution in leaves, stems, and roots. Proc. Natl Acad. Sci. USA 111, 13721–13726 (2014).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  24. De Frenne, P. et al. Latitudinal gradients as natural laboratories to infer species’ responses to temperature. J. Ecol. 101, 784–795 (2013).

    Article  Google Scholar 

  25. Luo, Y. Terrestrial carbon-cycle feedback to climate warming. Annu. Rev. Ecol. Evol. Syst. 38, 683–712 (2007).

    Article  Google Scholar 

  26. Jackson, R. B. et al. A global analysis of root distributions for terrestrial biomes. Oecologia 108, 389–411 (1996).

    Article  CAS  PubMed  Google Scholar 

  27. Malhi, Y., Doughty, C. & Galbraith, D. The allocation of ecosystem net primary productivity in tropical forests. Philos. Trans. R. Soc. Lond. B 366, 3225–3245 (2011).

    Article  CAS  Google Scholar 

  28. Roberts, D. R. et al. Cross-validation strategies for data with temporal, spatial, hierarchical, or phylogenetic structure. Ecography 40, 913–929 (2017).

    Article  Google Scholar 

  29. Cairns, M. A., Brown, S., Helmer, E. H. & Baumgardner, G. A. Root biomass allocation in the world’s upland forests. Oecologia 111, 1–11 (1997).

    Article  PubMed  Google Scholar 

  30. McCarthy, M. C. & Enquist, B. J. Consistency between an allometric approach and optimal partitioning theory in global patterns of plant biomass allocation. Funct. Ecol. 21, 713–720 (2007).

    Article  Google Scholar 

  31. Barton, C. V. M. & Montagu, K. D. Effect of spacing and water availability on root:shoot ratio in Eucalyptus camaldulensis. For. Ecol. Manage. 221, 52–62 (2006).

    Article  Google Scholar 

  32. Enquist, B. J. & Niklas, K. J. Global allocation rules for patterns of biomass partitioning in seed plants. Science 295, 1517–1520 (2002).

    Article  CAS  PubMed  Google Scholar 

  33. Goward, S. N., Tucker, C. J. & Dye, D. G. North American vegetation patterns observed with the NOAA-7 advanced very high resolution radiometer. Vegetatio 64, 3–14 (1985).

    Article  Google Scholar 

  34. Manzoni, S., Jackson, R. B., Trofymow, J. A. & Porporato, A. The global stoichiometry of litter nitrogen mineralization. Science 321, 684–686 (2008).

    Article  CAS  PubMed  Google Scholar 

  35. Kaiser, C., Franklin, O., Dieckmann, U. & Richter, A. Microbial community dynamics alleviate stoichiometric constraints during litter decay. Ecol. Lett. 17, 680–690 (2014).

    Article  PubMed  PubMed Central  Google Scholar 

  36. Jiao, F., Shi, X. R., Han, F. P. & Yuan, Z. Y. Increasing aridity, temperature and soil pH induce soil C-N-P imbalance in grasslands. Sci. Rep. 6, 19601 (2016).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  37. Sitch, S. et al. Recent trends and drivers of regional sources and sinks of carbon dioxide. Biogeosciences 12, 653–679 (2015).

    Article  Google Scholar 

  38. De Deyn, G. B., Cornelissen, J. H. C. & Bardgett, R. D. Plant functional traits and soil carbon sequestration in contrasting biomes. Ecol. Lett. 11, 516–531 (2008).

    Article  PubMed  Google Scholar 

  39. Tjoelker, M. G., Craine, J. M., Wedin, D., Reich, P. B. & Tilman, D. Linking leaf and root trait syndromes among 39 grassland and savannah species. New Phytol. 167, 493–508 (2005).

    Article  CAS  PubMed  Google Scholar 

  40. Personeni, E. & Loiseau, P. How does the nature of living and dead roots affect the residence time of carbon in the root litter continuum? Plant Soil 267, 129–141 (2004).

    Article  CAS  Google Scholar 

  41. Tuanmu, M. N. & Jetz, W. A global 1-km consensus land-cover product for biodiversity and ecosystem modelling. Glob. Ecol. Biogeogr. 23, 1031–1045 (2014).

    Article  Google Scholar 

  42. Pan, Y., Birdsey, R. A., Phillips, O. L. & Jackson, R. B. The structure, distribution, and biomass of the world’s forests. Annu. Rev. Ecol. Evol. Syst. 44, 593–622 (2013).

    Article  Google Scholar 

  43. Jackson, R. B., Mooney, H. A. & Schulze, E. D. A global budget for fine root biomass, surface area, and nutrient contents. Proc. Natl Acad. Sci. USA 94, 7362–7366 (1997).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  44. Genet, H., Bréda, N. & Dufrêne, E. Age-related variation in carbon allocation at tree and stand scales in beech (Fagus sylvatica L.) and sessile oak (Quercus petraea (Matt.) Liebl.) using a chronosequence approach. Tree Physiol. 30, 177–192 (2009).

    Article  PubMed  Google Scholar 

  45. De Castro, E. A. & Kauffman, J. B. Ecosystem structure in the Brazilian Cerrado: a vegetation gradient of aboveground biomass, root mass and consumption by fire. J. Trop. Ecol. 14, 263–283 (1998).

    Article  Google Scholar 

  46. Ding, B. & Sun, J. Study on biomass of Korean pine plantation in east mountain areas of northeast China. Bull. Bot. Res. 9, 149–157 (1989).

    Google Scholar 

  47. Ding, B., Liu, S. & Cai, T. Studies on biological productivity of artificial forests of Dahurian larches. Chin. J. Plant Ecol. 14, 226–236 (1990).

    Google Scholar 

  48. Ding, B. & Sun, J. Accumulation and distribution of productivity and nutrient element in natural Manchurian ash. J. Northeast For. Univ. 4, 1–9 (1989).

    Google Scholar 

  49. Dossa, E. L., Fernandes, E. C. M., Reid, W. S. & Ezui, K. Above- and belowground biomass, nutrient and carbon stocks contrasting an open-grown and a shaded coffee plantation. Agrofor. Syst. 72, 103–115 (2008).

    Article  Google Scholar 

  50. Epron, D. et al. Do changes in carbon allocation account for the growth response to potassium and sodium applications in tropical Eucalyptus plantations? Tree Physiol. 32, 667–679 (2012).

    Article  CAS  PubMed  Google Scholar 

  51. Fonseca, W., Rey Benayas, J. M. & Alice, F. E. Carbon accumulation in the biomass and soil of different aged secondary forests in the humid tropics of Costa Rica. For. Ecol. Manage. 262, 1400–1408 (2011).

    Article  Google Scholar 

  52. Goodman, R. C. et al. Amazon palm biomass and allometry. For. Ecol. Manage. 310, 994–1004 (2013).

    Article  Google Scholar 

  53. Greenland, D. J. & Kowal, J. M. L. Nutrient content of the moist tropical forest of Ghana. Plant Soil 12, 154–173 (1960).

    Article  CAS  Google Scholar 

  54. He, Y. et al. Carbon storage capacity of monoculture and mixed-species plantations in subtropical China. For. Ecol. Manage. 295, 193–198 (2013).

    Article  Google Scholar 

  55. Aiba, M. & Nakashizuka, T. Variation in juvenile survival and related physiological traits among dipterocarp species co‐existing in a Bornean forest. J. Veg. Sci. 18, 379–388 (2007).

    Article  Google Scholar 

  56. Jha, K. K. Carbon storage and sequestration rate assessment and allometric model development in young teak plantations of tropical moist deciduous forest, India. J. For. Res. 26, 589–604 (2015).

    Article  CAS  Google Scholar 

  57. Kalita, R. M., Das, A. K. & Nath, A. J. Allometric equations for estimating above- and belowground biomass in Tea (Camellia sinensis (L.) O. Kuntze) agroforestry system of Barak Valley, Assam, northeast India. Biomass Bioenergy 83, 42–49 (2015).

    Article  Google Scholar 

  58. Kenzo, T. et al. Development of allometric relationships for accurate estimation of above- and below-ground biomass in tropical secondary forests in Sarawak, Malaysia. J. Trop. Ecol. 25, 371–386 (2009).

    Article  Google Scholar 

  59. Kenzo, T. et al. Allometric equations for accurate estimation of above-ground biomass in logged-over tropical rainforests in Sarawak, Malaysia. J. For. Res. 14, 365–372 (2009).

    Article  CAS  Google Scholar 

  60. Kraenzel, M., Castillo, A., Moore, T. & Potvin, C. Carbon storage of harvest-age teak (Tectona grandis) plantations, Panama. For. Ecol. Manage. 173, 213–225 (2003).

    Article  Google Scholar 

  61. Kuyah, S., Dietz, J., Muthuri, C., van Noordwijk, M. & Neufeldt, H. Allometry and partitioning of above- and below-ground biomass in farmed eucalyptus species dominant in Western Kenyan agricultural landscapes. Biomass Bioenergy 55, 276–284 (2013).

    Article  Google Scholar 

  62. Liu, S., Cai, Y. & Cai, T. in Long-term Research on Forest Ecosystems (ed. Zhou, X.) 419–427 (Northeast Forestry Univ. Press, 1991).

  63. Luo, T. et al. Root biomass along subtropical to alpine gradients: global implication from Tibetan transect studies. For. Ecol. Manage. 206, 349–363 (2005).

    Article  Google Scholar 

  64. Markesteijn, L. & Poorter, L. Seedling root morphology and biomass allocation of 62 tropical tree species in relation to drought- and shade-tolerance. J. Ecol. 97, 311–325 (2009).

    Article  Google Scholar 

  65. McNicol, I. M. et al. Development of allometric models for above and belowground biomass in swidden cultivation fallows of northern Laos. For. Ecol. Manage. 357, 104–116 (2015).

    Article  Google Scholar 

  66. Aiba, M. & Nakashizuka, T. Sapling structure and regeneration strategy in 18 Shorea species co-occurring in a tropical rainforest. Ann. Bot. 96, 313–321 (2005).

    Article  PubMed  PubMed Central  Google Scholar 

  67. Menaut, J. C. & Cesar, J. Structure and primary productivity of Lamto savannas, Ivory Coast. Ecology 60, 1197–1210 (1979).

    Article  Google Scholar 

  68. Morais, V. A. et al. Estoques de carbono e biomassa de um fragmento de cerradão em Minas Gerais, Brasil. Cerne 19, 237–245 (2013).

    Article  Google Scholar 

  69. Mugasha, W. A. et al. Allometric models for prediction of above- and belowground biomass of trees in the miombo woodlands of Tanzania. For. Ecol. Manage. 310, 87–101 (2013).

    Article  Google Scholar 

  70. Návar, J. Plasticity of biomass component allocation patterns in semiarid Tamaulipan thornscrub and dry temperate pine species of northeastern Mexico. Polibotánica 31, 121–141 (2011).

    Google Scholar 

  71. Njana, M. A., Eid, T., Zahabu, E. & Malimbwi, R. Procedures for quantification of belowground biomass of three mangrove tree species. Wetl. Ecol. Manage. 23, 749–764 (2015).

    Article  Google Scholar 

  72. Nogueira Junior, L. R., Engel, V. L., Parrotta, J. A., de Melo, A. C. G. & Ré, D. S. Equações alométricas para estimativa da biomassa arbórea em plantios mistos com espécies nativas na restauração da Mata Atlântica. Biota Neotrop. 14, 1–9 (2014).

    Google Scholar 

  73. Peichl, M. & Arain, M. A. Above- and belowground ecosystem biomass and carbon pools in an age-sequence of temperate pine plantation forests. Agric. For. Meteorol. 140, e20130084 (2006).

    Article  Google Scholar 

  74. Battles, J. J. et al. Vegetation composition, structure, and biomass of two unpolluted watersheds in the Cordillera de Piuchué, Chiloé Island, Chile. Plant Ecol. 158, 5–19 (2002).

    Article  Google Scholar 

  75. Ryan, C. M., Williams, M. & Grace, J. Above- and belowground carbon stocks in a miombo woodland landscape of Mozambique. Biotropica 43, 423–432 (2011).

    Article  Google Scholar 

  76. Saint-André, L. et al. Age-related equations for above- and below-ground biomass of a Eucalyptus hybrid in Congo. For. Ecol. Manage. 205, 199–214 (2005).

    Article  Google Scholar 

  77. Aryal, D. R., De Jong, B. H. J., Ochoa-Gaona, S., Esparza-Olguin, L. & Mendoza-Vega, J. Carbon stocks and changes in tropical secondary forests of southern Mexico. Agric. Ecosyst. Environ. 195, 220–230 (2014).

    Article  Google Scholar 

  78. Schepaschenko, D. et al. A dataset of forest biomass structure for Eurasia. Sci. Data 4, 170070 (2017).

    Article  PubMed  PubMed Central  Google Scholar 

  79. Schroth, G., D’Angelo, S. A., Teixeira, W. G., Haag, D. & Lieberei, R. Conversion of secondary forest into agroforestry and monoculture plantations in Amazonia: consequences for biomass, litter and soil carbon stocks after 7 years. For. Ecol. Manage. 163, 131–150 (2002).

    Article  Google Scholar 

  80. Schulze, E. D. et al. Rooting depth, water availability, and vegetation cover along an aridity gradient in Patagonia. Oecologia 108, 503–511 (1996).

    Article  Google Scholar 

  81. Stolbovoi, V. & McCallum, I. Land resources of Russia [CD] (International Institute for Applied Systems Analysis and the Russian Academy of Science, 2002); http://www.iiasa.ac.at/Research/FOR/russia_cd/guide.htm

  82. Wang, L. et al. Biomass allocation patterns across China’s terrestrial biomes. PLoS ONE 9, e93566 (2014).

    Article  PubMed  PubMed Central  Google Scholar 

  83. Wauters, J. B., Coudert, S., Grallien, E., Jonard, M. & Ponette, Q. Carbon stock in rubber tree plantations in Western Ghana and Mato Grosso (Brazil). For. Ecol. Manage. 255, 2347–2361 (2008).

    Article  Google Scholar 

  84. Williams-Linera, G. Biomass and nutrient content in two successional stages of tropical wet forest in Uxpanapa, Mexico. Biotropica 15, 275–284 (1983).

    Article  Google Scholar 

  85. Xu, Y. et al. Improving allometry models to estimate the above- and belowground biomass of subtropical forest, China. Ecosphere 6, 289 (2015).

    Article  Google Scholar 

  86. Youkhana, A. H. & Idol, T. W. Allometric models for predicting above- and belowground biomass of Leucaena-KX2 in a shaded coffee agroecosystem in Hawaii. Agrofor. Syst. 83, 331–345 (2011).

    Article  Google Scholar 

  87. Zhang, H. et al. Biogeographical patterns of biomass allocation in leaves, stems, and roots in China’s forests. Sci. Rep. 5, 15997 (2015).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  88. Castellanos, J., Maass, M. & Kummerow, J. Root biomass of a dry deciduous tropical forest in Mexico. Plant Soil 131, 225–228 (1991).

    Article  Google Scholar 

  89. Zheng, Z., Feng, Z., Cao, M., Li, Z. & Zhang, J. Forest structure and biomass of a tropical seasonal rain forest in Xishuangbanna, southwest China. Biotropica 38, 318–327 (2006).

    Article  Google Scholar 

  90. Návar, J. Root stock biomass and productivity assessments of reforested pine stands in northern Mexico. For. Ecol. Manage. 338, 139–147 (2015).

    Article  Google Scholar 

  91. Wang, X., Fang, J. & Zhu, B. Forest biomass and root–shoot allocation in northeast China. For. Ecol. Manage. 255, 4007–4020 (2008).

    Article  Google Scholar 

  92. Chen, D. K., Zhou, X. F., Zhao, H. X., Wang, Y. H. & Jing, Y. Y. Study on the structure, function and succession of the four types in natural secondary forest. J. Northeast For. Univ. 2, 1–20 (1982).

    Google Scholar 

  93. Chidumayo, E. N. Estimating tree biomass and changes in root biomass following clear-cutting of Brachystegia-Julbernardia (miombo) woodland in central Zambia. Environ. Conserv. 41, 54–63 (2014).

    Article  Google Scholar 

  94. Coll, L., Potvin, C., Messier, C. & Delagrange, S. Root architecture and allocation patterns of eight native tropical species with different successional status used in open-grown mixed plantations in Panama. Trees 22, 585–596 (2008).

    Article  Google Scholar 

  95. Das, D. K. & Chaturvedi, O. P. Structure and function of Populus deltoides agroforestry systems in eastern India: 1. dry matter dynamics. Agrofor. Syst. 65, 215–221 (2005).

    Article  Google Scholar 

  96. Ni, J. Estimating net primary productivity of grasslands from field biomass measurements in temperate northern China. Plant Ecol. 174, 217–234 (2011).

    Article  Google Scholar 

  97. Olson, R. et al. NPP Multi-Biome: Summary Data from Intensive Studies at 125 Sites, 1936–2006 (ORNL DAAC, accessed 19 June 2019); https://daac.ornl.gov/cgi-bin/dsviewer.pl?ds_id=1352

  98. Perez, C. A. & Frangi, J. L. Grassland biomass dynamics along an altitudinal gradient in the pampa. J. Range Manage. 53, 518–528 (2007).

    Article  Google Scholar 

  99. Perez-Quezada, J. F. F., Delpiano, C. A. A., Snyder, K. A. A., Johnson, D. A. A. & Franck, N. Carbon pools in an arid shrubland in Chile under natural and afforested conditions. J. Arid Environ. 75, 29–37 (2011).

    Article  Google Scholar 

  100. Pornon, A., Boutin, M. & Lamaze, T. Contribution of plant species to the high N retention capacity of a subalpine meadow undergoing elevated N deposition and warming. Environ. Pollut. 245, 235–242 (2019).

    Article  CAS  PubMed  Google Scholar 

  101. Ramakrishnan, P. S. & Ram, S. C. Vegetation, biomass and productivity of seral grasslands of Cherrapunji in north-east India. Vegetatio 74, 47–53 (1988).

    Article  Google Scholar 

  102. Shaver, G. R., Laundre, J. A., Giblin, A. E. & Nadelhoffer, K. J. Changes in live plant biomass, primary production, and species composition along a riverside toposequence in Arctic Alaska, USA. Arct. Alp. Res. 28, 363–379 (2006).

    Article  Google Scholar 

  103. Smith, J. M. B. & Klinger, L. F. Aboveground:belowground phytomass ratios in Venezuelan paramo vegetation and their significance. Arct. Alp. Res. 17, 189–198 (2006).

    Article  Google Scholar 

  104. Sun, J. et al. Effects of grazing regimes on plant traits and soil nutrients in an alpine steppe, northern Tibetan Plateau. PLoS ONE 9, e108821 (2014).

    Article  PubMed  PubMed Central  Google Scholar 

  105. Wang, P. et al. Belowground plant biomass allocation in tundra ecosystems and its relationship with temperature. Environ. Res. Lett. 11, 055003 (2016).

    Article  Google Scholar 

  106. Yang, Y., Fang, J., Ji, C. & Han, W. Above- and belowground biomass allocation in Tibetan grasslands. J. Veg. Sci. 20, 177–184 (2009).

    Article  Google Scholar 

  107. Yang, Y., Fang, J., Ma, W., Guo, D. & Mohammat, A. Large-scale pattern of biomass partitioning across China’s grasslands. Glob. Ecol. Biogeogr. 19, 268–277 (2010).

    Article  Google Scholar 

  108. Geng, H. L., Wang, Y. H., Wang, F. Y. & Jia, B. R. The dynamics of root-shoot ratio and its environmental effective factors of recovering Leymus chinensis steppe vegetation in Inner Mongolia, China. Acta Ecol. Sin. 28, 4629–4634 (2008).

    Article  Google Scholar 

  109. Hui, D. & Jackson, R. B. Geographical and interannual variability in biomass partitioning in grassland ecosystems: a synthesis of field data. New Phytol. 169, 85–93 (2006).

    Article  CAS  PubMed  Google Scholar 

  110. Jouquet, P., Tavernier, V., Abbadie, L. & Lepage, M. Nests of subterranean fungus-growing termites (Isoptera, Macrotermitinae) as nutrient patches for grasses in savannah ecosystems. Afr. J. Ecol. 43, 191–196 (2005).

    Article  Google Scholar 

  111. Leonid, U. et al. Impact of climate and grazing on biomass components of eastern Russia typical steppe. J. Integr. Agric. 13, 1183–1192 (2014).

    Article  Google Scholar 

  112. Lucash, M. S., Farnsworth, B. & Winner, W. E. Response of sagebrush steppe species to elevated CO2 and soil temperature. West. N. Am. Nat. 65, 80–86 (2005).

    Google Scholar 

  113. Luo, W. et al. Patterns of plant biomass allocation in temperate grasslands across a 2500-km transect in northern China. PLoS ONE 8, e71749 (2013).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  114. Barbour, M. G. Desert dogma reexamined: root/shoot productivity and plant spacing. Am. Midl. Nat. 89, 41–57 (1973).

    Article  Google Scholar 

  115. Becker, P., Sharbini, N. & Yahya, R. Root architecture and root:shoot allocation of shrubs and saplings in two lowland tropical forests: implications for life-form composition. Biotropica 31, 93–101 (1999).

    Google Scholar 

  116. Becker, P. & Castillo, A. Root architecture of shrubs and saplings in the understory of a tropical moist forest in lowland Panama. Biotropica 22, 242–249 (1990).

    Article  Google Scholar 

  117. Beier, C. et al. Carbon and nitrogen balances for six shrublands across Europe. Glob. Biogeochem. Cycles 23, GB4008 (2009).

    Article  Google Scholar 

  118. Bhatt, Y. D., Rawat, Y. S. & Singh, S. P. Changes in ecosystem functioning after replacement of forest by Lantana shrubland in Kumaun Himalaya. J. Veg. Sci. 5, 67–70 (1994).

    Article  Google Scholar 

  119. Caldwell, M. M., White, R. S., Moore, R. T. & Camp, L. B. Carbon balance, productivity, and water use of cold-winter desert shrub communities dominated by C3 and C4 species. Oecologia 29, 275–300 (1977).

    Article  PubMed  Google Scholar 

  120. De Viñas, I. C. R. et al. Biomass of root and shoot systems of Quercus coccifera shrublands in eastern Spain. Ann. For. Sci. 57, 803–810 (2000).

    Article  Google Scholar 

  121. Caravaca, F., Figueroa, D., Alguacil, M. M. & Roldán, A. Application of composted urban residue enhanced the performance of afforested shrub species in a degraded semiarid land. Bioresour. Technol. 90, 65–70 (2003).

    Article  CAS  PubMed  Google Scholar 

  122. Caravaca, F., Figueroa, D., Azcón-Aguilar, C., Barea, J. M. & Roldán, A. Medium-term effects of mycorrhizal inoculation and composted municipal waste addition on the establishment of two Mediterranean shrub species under semiarid field conditions. Agric. Ecosyst. Environ. 97, 95–105 (2003).

    Article  Google Scholar 

  123. Carrasco, L., Azcón, R., Kohler, J., Roldán, A. & Caravaca, F. Comparative effects of native filamentous and arbuscular mycorrhizal fungi in the establishment of an autochthonous, leguminous shrub growing in a metal-contaminated soil. Sci. Total Environ. 409, 1205–1209 (2011).

    Article  CAS  PubMed  Google Scholar 

  124. Carrillo-Garcia, Á., Bashan, Y. & Bethlenfalvay, G. J. Resource-island soils and the survival of the giant cactus, cardon, of Baja California Sur. Plant Soil 218, 207–214 (2000).

    Article  CAS  Google Scholar 

  125. Carrión-Prieto, P. et al. Mediterranean shrublands as carbon sinks for climate change mitigation: new root-to-shoot ratios. Carbon Manage. 8, 67–77 (2017).

    Article  Google Scholar 

  126. Deng, L., Han, Q. S., Zhang, C., Tang, Z. S. & Shangguan, Z. P. Above-ground and below-ground ecosystem biomass accumulation and carbon sequestration with Caragana korshinskii Kom plantation development. Land Degrad. Dev. 28, 906–917 (2017).

    Article  Google Scholar 

  127. Perkins, S. R. & Owens, M. K. Growth and biomass allocation of shrub and grass seedlings in response to predicted changes in precipitation seasonality. Plant Ecol. 168, 107–120 (2003).

    Article  Google Scholar 

  128. Gargaglione, V., Peri, P. L. & Rubio, G. Allometric relations for biomass partitioning of Nothofagus antarctica trees of different crown classes over a site quality gradient. For. Ecol. Manage. 259, 1118–1126 (2010).

    Article  Google Scholar 

  129. Hao, H. M. et al. Effects of shrub patch size succession on plant diversity and soil water content in the water-wind erosion crisscross region on the Loess Plateau. Catena 144, 177–183 (2016).

    Article  Google Scholar 

  130. Herwitz, S. R. & Olsvig-Whittaker, L. Preferential upslope growth of Zygophyllum dumosum Boiss. (Zygophyllaceae) roots into bedrock fissures in the northern Negev desert. J. Biogeogr. 16, 457–460 (1989).

    Article  Google Scholar 

  131. Hoffmann, A. & Kummerow, J. Root studies in the Chilean matorral. Oecologia 32, 57–69 (1978).

    Article  PubMed  Google Scholar 

  132. Holl, K. D. Effects of above- and below-ground competition of shrubs and grass on Calophyllum brasiliense (Camb.) seedling growth in abandoned tropical pasture. For. Ecol. Manage. 109, 187–195 (1998).

    Article  Google Scholar 

  133. Hollister, R. D. & Flaherty, K. J. Above- and below-ground plant biomass response to experimental warming in northern Alaska. Appl. Veg. Sci. 13, 378–387 (2010).

    Google Scholar 

  134. Kizito, F. et al. Seasonal soil water variation and root patterns between two semi-arid shrubs co-existing with pearl millet in Senegal, West Africa. J. Arid Environ. 67, 436–455 (2006).

    Article  Google Scholar 

  135. Kummerow, J., Krause, D. & Jow, W. Root systems of chaparral shrubs. Oecologia 29, 163–177 (1977).

    Article  PubMed  Google Scholar 

  136. León, M. F., Squeo, F. A., Gutiérrez, J. R. & Holmgren, M. Rapid root extension during water pulses enhances establishment of shrub seedlings in the Atacama Desert. J. Veg. Sci. 22, 120–129 (2011).

    Article  Google Scholar 

  137. Li, C. P. & Xiao, C. W. Above- and belowground biomass of Artemisia ordosica communities in three contrasting habitats of the Mu Us Desert, northern China. J. Arid Environ. 70, 195–207 (2007).

    Article  Google Scholar 

  138. Liang, Y. M., Hazlett, D. L. & Lauenroth, W. K. Biomass dynamics and water use efficiencies of five plant communities in the shortgrass steppe. Oecologia 80, 148–153 (1989).

    Article  CAS  PubMed  Google Scholar 

  139. Zan, Q., Wang, Y., Liao, B. & Zheng, D. Biomass and net productivity of Sonneratia apetala, S. caseolaris mangrove man-made forest. Wuhan Bot. Res. 19, 391–396 (2001).

    Google Scholar 

  140. Liao, B., Zheng, D. & Zheng, S. Studies on the biomass of Sonneratia caseolaris stand. For. Res. 3, 47–54 (1990).

    Google Scholar 

  141. Lufafa, A. et al. Allometric relationships and peak-season community biomass stocks of native shrubs in Senegal’s Peanut Basin. J. Arid Environ. 73, 260–266 (2009).

    Article  Google Scholar 

  142. Lusk, C. H. Leaf area and growth of juvenile temperate evergreens in low light: species of contrasting shade tolerance change rank during ontogeny. Funct. Ecol. 18, 820–828 (2004).

    Article  Google Scholar 

  143. Marsh, A. S., Arnone, J. A., Bormann, B. T. & Gordon, J. C. The role of Equisetum in nutrient cycling in an Alaskan shrub wetland. J. Ecol. 88, 999–1011 (2000).

    Article  Google Scholar 

  144. Martínez, F. et al. Belowground structure and production in a Mediterranean sand dune shrub community. Plant Soil 201, 209–216 (1998).

    Article  Google Scholar 

  145. Marziliano, P. A. et al. Estimating belowground biomass and root/shoot ratio of Phillyrea latifolia L. in the Mediterranean forest landscapes. Ann. For. Sci. 72, 585–593 (2015).

    Article  Google Scholar 

  146. Mauchamp, A., Montaña, C., Lepart, J., Rambal, S. & Montana, C. Ecotone dependent recruitment of a desert shrub, Flourensia cernua, in vegetation stripes. Oikos 68, 107–116 (1993).

    Article  Google Scholar 

  147. Mendoza-Ponce, A. & Galicia, L. Aboveground and belowground biomass and carbon pools in highland temperate forest landscape in central Mexico. Forestry 83, 497–506 (2010).

    Article  Google Scholar 

  148. Miller, P. C. & Ng, E. Root:shoot biomass ratios in shrubs in southern California and central Chile. Madrono 24, 215–223 (1977).

    Google Scholar 

  149. Mooney, H. A. & Rundel, P. W. Nutrient relations of the evergreen shrub, Adenostoma fasciculatum, in the California chaparral. Bot. Gaz. 140, 109–113 (1979).

    Article  CAS  Google Scholar 

  150. Moro, M. J., Pugnaire, F. I., Haase, P. & Puigdefábregas, J. Effect of the canopy of Retama sphaerocarpa on its understorey in a semiarid environment. Funct. Ecol. 11, 425–431 (1997).

    Article  Google Scholar 

  151. Negreiros, D., Fernandes, G. W., Silveira, F. A. O. & Chalub, C. Seedling growth and biomass allocation of endemic and threatened shrubs of rupestrian fields. Acta Oecol. 35, 301–310 (2009).

    Article  Google Scholar 

  152. Nie, X., Yang, Y., Yang, L. & Zhou, G. Above- and belowground biomass allocation in shrub biomes across the northeast Tibetan Plateau. PLoS ONE 11, e0154251 (2016).

    Article  PubMed  PubMed Central  Google Scholar 

  153. Nobel, P. S., Quero, E. & Linares, H. Root versus shoot biomass: responses to water, nitrogen, and phosphorus applications for Agave lechuguilla. Bot. Gaz. 150, 411–416 (1989).

    Article  Google Scholar 

  154. Pacaldo, R. S., Volk, T. A. & Briggs, R. D. Greenhouse gas potentials of shrub willow biomass crops based on below- and aboveground biomass inventory along a 19-year chronosequence. Bioenergy Res. 6, 252–262 (2013).

    Article  CAS  Google Scholar 

  155. Padilla, F. M., Miranda, J. D., Jorquera, M. J. & Pugnaire, F. I. Variability in amount and frequency of water supply affects roots but not growth of arid shrubs. Plant Ecol. 204, 261–270 (2009).

    Article  Google Scholar 

  156. Portsmuth, A., Niinemets, Ü., Truus, L. & Pensa, M. Biomass allocation and growth rates in Pinus sylvestris are interactively modified by nitrogen and phosphorus availabilities and by tree size and age. Can. J. For. Res. 35, 2346–2359 (2005).

    Article  CAS  Google Scholar 

  157. Roth, G. A., Whitford, W. G. & Steinberger, Y. Jackrabbit (Lepus californicus) herbivory changes dominance in desertified Chihuahuan Desert ecosystems. J. Arid Environ. 70, 418–426 (2007).

    Article  Google Scholar 

  158. Ruiz-Peinado, R., Moreno, G., Juarez, E., Montero, G. & Roig, S. The contribution of two common shrub species to aboveground and belowground carbon stock in Iberian dehesas. J. Arid Environ. 91, 22–30 (2013).

    Article  Google Scholar 

  159. Rundel, P. W. Biomass, productivity, and nutrient allocation in subalpine shrublands and meadows of the Emerald Lake Basin, Sequoia National Park, California. Arct. Antarct. Alp. Res. 47, 115–123 (2015).

    Article  Google Scholar 

  160. Millikin, C. S. & Bledsoe, C. S. Biomass and distribution of fine and coarse roots from blue oak (Quercus douglasii) trees in the northern Sierra Nevada foothills of California. Plant Soil 214, 27–38 (1999).

    Article  CAS  Google Scholar 

  161. Saura-Mas, S. & Lloret, F. Adult root structure of Mediterranean shrubs: relationship with post-fire regenerative syndrome. Plant Biol. 16, 147–154 (2014).

    Article  CAS  PubMed  Google Scholar 

  162. Schenk, H. J. & Mahall, B. E. Positive and negative plant interactions contribute to a north-south-patterned association between two desert shrub species. Oecologia 132, 402–410 (2002).

    Article  PubMed  Google Scholar 

  163. Silva, J. S., Rego, F. C. & Martins-Loução, M. A. Belowground traits of Mediterranean woody plants in a Portuguese shrubland. Ecol. Mediterr. 28, 5–13 (2002).

    Article  Google Scholar 

  164. Simões, M. P., Madeira, M. & Gazarini, L. Biomass and nutrient dynamics in Mediterranean seasonal dimorphic shrubs: strategies to face environmental constraints. Plant Biosyst. 146, 500–510 (2012).

    Google Scholar 

  165. Tao, Y., Zhang, Y. M. & Downing, A. Similarity and difference in vegetation structure of three desert shrub communities under the same temperate climate but with different microhabitats. Bot. Stud. 54, 59 (2013).

    Article  PubMed  PubMed Central  Google Scholar 

  166. Toscano, S., Scuderi, D., Giuffrida, F. & Romano, D. Responses of Mediterranean ornamental shrubs to drought stress and recovery. Sci. Hortic. 178, 145–153 (2014).

    Article  Google Scholar 

  167. Trubat, R., Cortina, J. & Vilagrosa, A. Nutrient deprivation improves field performance of woody seedlings in a degraded semi-arid shrubland. Ecol. Eng. 37, 1164–1173 (2011).

    Article  Google Scholar 

  168. Van Wijk, M. T., Williams, M., Gough, L., Hobbie, S. E. & Shaver, G. R. Luxury consumption of soil nutrients: a possible competitive strategy in above-ground and below-ground biomass allocation and root morphology for slow-growing arctic vegetation? J. Ecol. 91, 664–676 (2003).

    Article  Google Scholar 

  169. Walker, L. R., Clarkson, B. D., Silvester, W. B. & Clarkson, B. R. Colonization dynamics and facilitative impacts of a nitrogen-fixing shrub in primary succession. J. Veg. Sci. 14, 277–290 (2003).

    Article  Google Scholar 

  170. Wang, B. & Yang, X. S. Comparison of biomass and species diversity of four typical zonal vegetations. J. Fujian Coll. For. 29, 345–350 (2009).

    Google Scholar 

  171. Wang, M. & Li, H. Quantitative study on the soil water dynamics of various forest plantations in the Loess Plateau region in northwestern Shanxi. Acta Ecol. Sin. 2, 178–184 (1995).

    Google Scholar 

  172. Wang, P. et al. Seasonal changes and vertical distribution of root standing biomass of graminoids and shrubs at a Siberian tundra site. Plant Soil 407, 55–65 (2016).

    Article  CAS  Google Scholar 

  173. Whittaker, R. H. & Woodwell, G. M. Dimension and production relations of trees and shrubs in the Brookhaven Forest, New York. J. Ecol. 56, 1–25 (1968).

    Article  Google Scholar 

  174. Xu, H., Li, Y., Xu, G. & Zou, T. Ecophysiological response and morphological adjustment of two Central Asian desert shrubs towards variation in summer precipitation. Plant Cell Environ. 30, 399–409 (2007).

    Article  CAS  PubMed  Google Scholar 

  175. Yan, Z. Biomass and its allocation in a 28-year-old Castanopsis kawakamii plantation. J. Fujian Coll. For. 2, 114–118 (1996).

    Google Scholar 

  176. Gong, Y. et al. Carbon storage and vertical distribution in three shrubland communities in Gurbantünggüt Desert, Uygur Autonomous Region of Xinjiang, northwest China. Chin. Geogr. Sci. 22, 541–549 (2012).

    Article  Google Scholar 

  177. Yu, Y., Shi, D., Qiuyi, J., He, L. & Cheng, G. On the biomass of secondary Schima superba forest in Hangzhou. J. Zhejiang For. Coll. 2, 157–161 (1993).

    Google Scholar 

  178. Kato, T. et al. Carbon dioxide exchange between the atmosphere and an alpine meadow ecosystem on the Qinghai-Tibetan Plateau, China. Agric. Meteorol. 124, 121–134 (2004).

    Article  Google Scholar 

  179. Li, Z., Zhu, Q. & Li, J. A comparison of photosynthetic carbon sequestration of four shrubs in Ningxia. Pratacultural Sci. 29, 352–357 (2012).

    CAS  Google Scholar 

  180. Zhu, X., Shi, Q. & Li, Y. A preliminary study on the Qinghai’s treasure house of the forest biomass and shrubs. Sci. Technol. Qinghai Agric. For. 1, 15–20 (1993).

    Google Scholar 

  181. Liao, B. & Zheng, D. Study on the forest biomass and productivity of olive wood. For. Res. 4, 22–29 (1991).

    Google Scholar 

  182. Liu, B., Liu, Z., Lü, X., Maestre, F. T. & Wang, L. Sand burial compensates for the negative effects of erosion on the dune-building shrub Artemisia wudanica. Plant Soil 374, 263–273 (2014).

    Article  CAS  Google Scholar 

  183. Alguacil, M. M., Hernández, J. A., Caravaca, F., Portillo, B. & Roldán, A. Antioxidant enzyme activities in shoots from three mycorrhizal shrub species afforested in a degraded semi-arid soil. Physiol. Plant. 118, 562–570 (2003).

    Article  CAS  Google Scholar 

  184. Axe, M. S., Grange, I. D. & Conway, J. S. Carbon storage in hedge biomass—a case study of actively managed hedges in England. Agric. Ecosyst. Environ. 250, 81–88 (2017).

    Article  Google Scholar 

  185. van den Hoogen, J. et al. Soil nematode abundance and functional group composition at a global scale. Nature 572, 194–198 (2019).

    Article  PubMed  Google Scholar 

  186. Erin, L. et al. h2o: R Interface for the ‘H2O’ Scalable Machine Learning Platform. R package v.3.32.0.2 (2020); https://github.com/h2oai/h2o-3

  187. Sagi, O. & Rokach, L. Ensemble learning: a survey. WIREs Data Min. Knowl. Discov. 8, e1249 (2018).

    Google Scholar 

  188. R Core Team. R: A Language and Environment for Statistical Computing (R Foundation for Statistical Computing, 2019).

  189. Gorelick, N. et al. Google Earth Engine: planetary-scale geospatial analysis for everyone. Remote Sens. Environ. 202, 18–27 (2017).

    Article  Google Scholar 

  190. Heiberger, R. M. HH: Statistical Analysis and Data Display: Heiberger and Holland (2020).

  191. Hothorn, T. & Zeileis, A. partykit: A modular toolkit for recursive partytioning in R. J. Mach. Learn. Res. 16, 3905–3909 (2015).

    Google Scholar 

  192. Borkovec, M. & Madin, N. ggparty: ‘ggplot’ visualizations for the ‘partykit’ package (2019).

  193. Dormann, C. F. Effects of incorporating spatial autocorrelation into the analysis of species distribution data. Glob. Ecol. Biogeogr. 16, 129–138 (2007).

    Article  Google Scholar 

  194. Hutchinson, M., Xu, T., Houlder, D., Nix, H. & McMahon, J. ANUCLIM 6.0 User’s Guide (Australian National Univ., 2009).

  195. Fick, S. E. & Hijmans, R. J. WorldClim 2: new 1-km spatial resolution climate surfaces for global land areas. Int. J. Climatol. 37, 4302–4315 (2017).

    Article  Google Scholar 

  196. Global Aridity and PET database (CGIAR-CSI, accessed 15 May 2018); http://www.cgiarcsi.community/data/global-aridity-and-pet-database

  197. CIESIN Gridded Population of the World, version 4 (GPWv4): Population Density Adjusted to Match 2015 Revision UN WPP Country Totals (NASA SEDAC, 2018); https://doi.org/10.7927/H4HX19NJ

  198. Venter, O. et al. Global terrestrial human footprint maps for 1993 and 2009. Sci. Data 3, 160067 (2016).

    Article  PubMed  PubMed Central  Google Scholar 

  199. SoilGrids (ISRIC, accessed 15 May 2018); https://www.soilgrids.org

  200. Entekhabi, D. et al. The soil moisture active passive (SMAP) mission. Proc. IEEE 98, 704–716 (2010).

    Article  Google Scholar 

  201. Fan, Y., Li, H. & Miguez-Macho, G. Global patterns of groundwater table depth. Science 339, 940–943 (2013).

    Article  CAS  PubMed  Google Scholar 

  202. Batjes, N. H. Harmonized soil property values for broad-scale modelling (WISE30sec) with estimates of global soil carbon stocks. Geoderma 269, 61–68 (2016).

    Article  CAS  Google Scholar 

  203. Schaaf, C. & Wang, Z. MCD43A1 MODIS/Terra+Aqua BRDF/Albedo Model Parameters Daily L3 Global - 500m V006 (NASA LP DAAC, 2015); https://doi.org/10.5067/MODIS/MCD43A1C.006

  204. Didan, K. MOD13Q1 MODIS/Terra Vegetation Indices 16-Day L3 Global 250m SIN Grid V006 (NASA LP DAAC, 2015).

  205. Crowther, T. W. et al. Mapping tree density at a global scale. Nature 525, 201–205 (2015).

    Article  CAS  PubMed  Google Scholar 

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Acknowledgements

We thank J.-F. Bastin, P. B. Reich, R. B. Jackson and Y. Zeng for their constructive comments on this study. This work was supported by grants to C.M.Z. from the ETH Zurich Postdoctoral Fellowship programme, L.M. from the China Scholarship Council and T.W.C. from DOB Ecology. B.D.S. was funded by the Swiss National Science Foundation grant no. PCEFP2_181115. C.T. was supported by a Lawrence Fellow award through the Lawrence Livermore National Laboratory, the US Department of Energy under contract DE-AC52-07NA27344 and the Lawrence Livermore National Laboratory LDRD (Laboratory Directed Research & Development) Program under project no. 20-ERD-055.

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H.M., L.M., T.W.C. and C.M.Z. conceived and developed the study and wrote the manuscript. H.M. and L.M. collected the data. H.M. and L.M. performed the analyses. D.S.M., J.v.d.H., B.S. and C.T. gave input on the manuscript.

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Correspondence to Constantin M. Zohner.

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Extended data

Extended Data Fig. 1

Information on the 63 selected covariate layers used to model root mass fractions194,195,196,197,198,199,200,201,202,203,204,205.

Extended Data Fig. 2 Random 10-fold cross-validation (RCV) of the spatial root-mass fraction models and spatial autocorrelation of model residuals.

a–c, Heat plots showing the relationships between predicted and observed RMFs in forests (a), shrublands (b), and grasslands (c) based on RCV. Solid lines indicate fitted relationships based on ordinary least squares regression [coefficient of determination values relative to the 1:1 line (equation 2) shown in the bottom right corner], dashed diagonal lines indicate a 1:1 relationship between observed and predicted points. d–f, The standard errors of the observed (black) and predicted (grey) mean values of root mass fractions decrease with increasing sample size. The operation was repeated with 1,000 random seeds for the observed and predicted mean values, and the calculated standard errors of the mean are shown. Note, ‘sample size’ in D–F refers to the number of pixels, and thus denotes square kilometres. g–i, Semivariograms illustrating spatial autocorrelation of model residuals in forests (g), shrublands (h) and grasslands (i). Semivariances of residuals were computed based on random 10-fold cross validation (blue) and spatial leave-one-out cross-validation (LOO-CV) with buffer radii of 150km (dark green), 250km (green) and 500km (light green). Dashed vertical lines indicate the buffer radii of the final validation model reported throughout the text.

Extended Data Fig. 3 Partial regression coefficients for the effects of 8 environmental covariates from linear multiple regression models.

To reduce the influence of spatial autocorrelation, a bootstrapping procedure was applied for the forest data (see Methods). Red dots indicate positive effects on RMFs, blue dots indicate negative effects. Error bars reflect two standard errors either side of the mean partial regression coefficient.

Extended Data Fig. 4 Recursive partitioning trees for the univariate effects of annual mean temperature (a), soil moisture (b), NDVI (c), and sand content (d) on RMFs in forests.

These four variables were chosen on basis of the random forest variable importance metric (Fig. 3a) and, for each model, the remaining three variables were evaluated as potential split points. The number of independent observations contained in each terminal node was constrained to ≥10% of the total data (500 observations). Regression plots show slopes and 95% confidence intervals.

Extended Data Fig. 5 Recursive partitioning trees for the univariate effects of annual mean temperature (a), soil moisture (b), aridity index (c), and NDVI (d) on RMFs in shrublands.

These four variables were chosen on basis of the random forest variable importance metric (Fig. 3b) and, for each model, the remaining three variables were evaluated as potential split points. The number of independent observations contained in each terminal node was constrained to ≥10% of the total data (30 observations). Regression plots show slopes and 95% confidence intervals.

Extended Data Fig. 6 Recursive partitioning trees for the univariate effects of annual mean temperature (a), soil moisture (b), aridity index (c), and NDVI (d) on RMFs in grasslands.

These four variables were chosen on basis of the random forest variable importance metric (Fig. 3c) and, for each model, the remaining three variables were evaluated as potential split points. The number of independent observations contained in each terminal node was constrained to ≥10% of the total data (120 observations). Regression plots show slopes and 95% confidence intervals.

Extended Data Fig. 7 Comparison of observed forest RMFs with predicted RMFs from dynamic global vegetation models and a current-generation biomass map.

The blue bars represent histograms of predicted RMF values based on our LOO-CV procedure (a), current-generation biomass estimates6 (b), and the vegetation models CABLE-POP (c), CLASS-CTEM (d), ISAM (e) and ORCHIDEE (f). Yellow bars represent observed values. Insets show scatter plots of predicted versus observed RMFs with solid lines indicating fitted relationships, dashed diagonal lines indicating a 1:1 relationship between observed and predicted points. For the vegetation models, forest was defined as pixels with a tree cover fraction higher than 50%.

Extended Data Fig. 8 The global distribution of belowground plant biomass and associated uncertainties in forests (a, b), grasslands (c, d), and shrublands (e, f).

a, c, e, Belowground plant biomass (in tons carbon per hectare). b, d, f Associated uncertainties in belowground carbon, calculated as the predicted biomass range (based on 2.5% and 97.5% RMF quantiles derived from the bootstrapped RMF models) divided by the mean predicted biomass in each pixel. Maps are projected at 30 arc-seconds (~1 km2) resolution.

Extended Data Fig. 9 Root mass fraction inter-model consistency in forests (a), grasslands (b) and shrublands (c).

Inter-model consistency was calculated as the coefficient of variation (standard deviation divided by mean, in %) of the predictions of the 10 best models. Maps are projected at 30 arc-seconds (~1 km2) resolution.

Extended Data Fig. 10 The extent of interpolation and extrapolation across all terrestrial pixels in which the respective vegetation type, forest (a), grassland (b) and shrubland (c) occurs.

Values represent the percentage of interpolation based on principal component analysis, that is, the percentage of bands that fall into the convex hull space.

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Ma, H., Mo, L., Crowther, T.W. et al. The global distribution and environmental drivers of aboveground versus belowground plant biomass. Nat Ecol Evol 5, 1110–1122 (2021). https://doi.org/10.1038/s41559-021-01485-1

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