Ants are one of the most abundant and ubiquitous organisms on Earth and play critical roles in multiple ecosystem services such as seed dispersal and nutrient cycling. Despite this, the effects of climatic and land use stressors on particular species or groups of ants are poorly known. We conducted a regional field survey across 108 locations in south-eastern Australia, using correlation network analysis and structural equation modelling to identify how ants respond to environmental stressors. We found contrasting relationships amongst ants, and aridity, and vertebrate grazing intensity and history. Increasing aridity was associated with reduced ant richness, whereas increasing grazing intensity was associated with greater ant richness directly, and indirectly, via reductions in litter depth and perennial grass density. However, these taxonomically diverse groups of ant species still shared contrasting responses to increasing aridity and grazing intensity. We found strong associations between grazing, aridity and the abundance of Seed Harvesters, weak indirect relationships with Generalist Foragers, but no relationships for Predators or Sugar Feeders. Taken together, our work identifies contrasting relationships amongst grazing, aridity and ants (ant 'winners' or 'losers') across contrasting ecological contexts. Given that increasing aridity is generally associated with lower grazing intensity, our results suggest that locations with more arid sites will have lower ant richness with fewer Seed Harvesters, whereas more mesic sites with high grazing intensity might increase ant richness, and the abundance of specific ant species. Such knowledge is important if we are to maintain critical ant-mediated functions as Earth becomes drier and grazing intensity increases. ; M.D-B. was supported by the European Union's Horizon 2020 research and innovation programme under the Marie Sklodowska-Curie Grant Agreement No 702057 (CLIMIFUN) and by a Large Research Grant from the British Ecological Society (Grant Agreement No. ...
Aim: Soil microbes are essential for maintenance of life‐supporting ecosystem services, but projections of how these microbes will be affected by global change scenarios are lacking. Therefore, our aim was to provide projections of future soil microbial distribution using several scenarios of global change. Location: Global. Time period: 1950–2090. Major taxa studied: Bacteria and fungi. Methods: We used a global database of soil microbial communities across six continents to estimate past and future trends of the soil microbiome. To do so, we used structural equation models to include the direct and indirect effects of changes in climate and land use in our predictions, using current climate (temperature and precipitation) and land‐use projections between 1950 and 2090. Results: Local bacterial richness will increase in all scenarios of change in climate and land use considered, although this increase will be followed by a generalized community homogenization process affecting > 85% of terrestrial ecosystems. Changes in the relative abundance of functional genes associated with the increases in bacterial richness are also expected. Based on an ecological cluster analysis, our results suggest that phylotypes such as Geodermatophilus spp. (typical desert bacteria), Mycobacterium sp. (which are known to include important human pathogens), Streptomyces mirabilis (major producers of antibiotic resistance genes) or potential fungal soil‐borne plant pathogens belonging to Ascomycota fungi (Venturia spp., Devriesia spp.) will become more abundant in their communities. Main conclusions: Our results provide evidence that climate change has a stronger influence on soil microbial communities than change in land use (often including deforestation and agricultural expansion), although most of the effects of climate are indirect, through other environmental variables (e.g., changes in soil pH). The same was found for microbial functions such as the prevalence of phosphate transport genes. We provide reliable predictions about the changes in the global distribution of microbial communities, showing an increase in alpha diversity and a homogenization of soil microbial communities in the Anthropocene. ; This manuscript was developed from discussions within the German Centre of Integrative Biodiversity Research funded by the Deutsche Forschungsgemeinschaft (DFG FZT118). C.A.G. and N.E. acknowledge funding by iDiv (DFG FZT118) Flexpool proposals 34600850 and 34600844. N.E. acknowledges funding by the DFG (FOR 1451) and the European Research Council (ERC) under the European Union's Horizon 2020 research and innovation programme (grant agreement no. 677232). E.D. acknowledges funding by the Deutsche Forschungsgemeinschaft (DFG GRK 2297 –314838170), MathCoRe. M.D.-B. acknowledges support from the Marie Sklodowska-Curie Actions of the Horizon 2020 Framework Program H2020-MSCA-IF-2016 under REA grant agreement number 702057. F.T.M. acknowledges support from the European Research Council grant agreement number 647038 (BIODESERT).
The relationship between biodiversity and biomass has been a long standing debate in ecology. Soil biodiversity and biomass are essential drivers of ecosystem functions. However, unlike plant communities, little is known about how the diversity and biomass of soil microbial communities are interlinked across globally distributed biomes, and how variations in this relationship influence ecosystem function. To fill this knowledge gap, we conducted a field survey across global biomes, with contrasting vegetation and climate types. We show that soil carbon (C) content is associated to the microbial diversity–biomass relationship and ratio in soils across global biomes. This ratio provides an integrative index to identify those locations on Earth wherein diversity is much higher compared with biomass and vice versa. The soil microbial diversity-to-biomass ratio peaks in arid environments with low C content, and is very low in C-rich cold environments. Our study further advances that the reductions in soil C content associated with land use intensification and climate change could cause dramatic shifts in the microbial diversity-biomass ratio, with potential consequences for broad soil processes. ; We would like to thank the researchers involved in the CLIMIFUN project for the help with soil sampling. This project has received funding from the European Union's Horizon 2020 research and innovation program under the Marie Sklodowska-Curie grant agreement no. 702057. FB and CG thank the Spanish Ministry and FEDER funds for the project AGL2017–85755-R MINECO/AEI/FEDER, UE; the i-LINK + 2018 (LINKA20069) from CSIC, and funds from "Fundación Séneca" from Murcia Province (19896/GERM/15). MD-B is supported by a Ramón y Cajal grant from the Spanish Ministry of Science and Innovation (RYC2018-025483-I). RDB was supported by NERC Soil Security program grants NE/M017028/1 and NE/P013708/1
1. Plant‐associated microbes play essential roles in nutrient uptake and plant productivity, but their role in driving plant germination, a critical stage in the plant life cycle, is still poorly understood. 2. We used data from a large‐scale, field‐based soil seed bank study to examine the relationship among plants germinating from the seed bank and soil microbial community composition. We combined this with an experiment using 34 laboratory‐based microcosms whereby sterile soil was inoculated with microbes from different field sites to examine how microbes affect the germination of nine plant species. 3. The community composition of plants in the soil seed bank was highly and significantly associated with bacterial and fungal community composition, with stronger correlations for soil beneath plant canopies. Microbes predicted a unique portion of the variation in the community composition of germinants after accounting for differences in environmental variables. The strongest correlations among microbes and plant functional traits included those related to perenniality, growth form, plant size, root type and seed shape. Our microcosm study showed that different plant species had their own associated germination microbiome, and most plant–microbe interactions were positive during germination. 4. Synthesis. Our study provides evidence for intimate relationships between plant and soil biodiversity during germination. Our work fills an important knowledge gap for plant–microbe interactions and reveals valuable insights into the shared natural history of plants and microbes in terrestrial ecosystems. ; M.D.-B. was supported by the European Union's Horizon 2020 research and innovation program under the Marie Sklodowska-Curie Grant Agreement No 702057 (CLIMIFUN) and by a Large Research Grant from the British Ecological Society (Grant Agreement No. LRA17\1193, MUSGONET).
Soil carbon losses to the atmosphere, via soil heterotrophic respiration, are expected to increase in response to global warming, resulting in a positive carbon-climate feedback. Despite the well-known suite of abiotic and biotic factors controlling soil respiration, much less is known about how the magnitude of soil respiration responses to temperature changes over soil development and across contrasting soil properties. Here we investigated the role of soil development stage and soil properties in driving the responses of soil heterotrophic respiration to temperature. We incubated soils from eight chronosequences ranging in soil age from hundreds to million years, and encompassing a wide range of vegetation types, climatic conditions and chronosequences origins, at three assay temperatures (5 °C, 15 °C and 25 °C). We found a consistent positive effect of assay temperature on soil respiration rates across the eight chronosequences evaluated. However, chronosequences parent materials (sedimentary/sand dunes or volcanic) and soil properties (pH, phosphorus content and microbial biomass) determined the magnitude of this temperature effect. Finally, we observed a positive effect of soil development stage on soil respiration across chronosequences that did not alter the magnitude of assay temperature effects. Our work reveals that key soil properties alter the magnitude of the positive effect of temperature on soil respiration found across ecosystem types and soil development stages. This information is essential to better understand the magnitude of the carbon-climate feedback and thus to establish accurate greenhouse gas emission targets. ; This research received funding from the European Union's Horizon 2020 research and innovation program under Marie Sklodowska-Curie Grant Agreement 702057. M.D. was supported by an FPU fellowship from the Spanish Ministry of Education, Culture and Sports (FPU-15/00392). M.D. and F.T.M. are supported by the European Research Council (Consolidator Grant Agreement No 647038, ...
Understanding the present and future distribution of soil-borne plant pathogens is critical to supporting food and fibre production in a warmer world. Using data from a global field survey and a nine-year field experiment, we show that warmer temperatures increase the relative abundance of soil-borne potential fungal plant pathogens. Moreover, we provide a global atlas of these organisms along with future distribution projections under different climate change and land-use scenarios. These projections show an overall increase in the relative abundance of potential plant pathogens worldwide. This work advances our understanding of the global distribution of potential fungal plant pathogens and their sensitivity to ongoing climate and land-use changes, which is fundamental to reduce their incidence and impacts on terrestrial ecosystems globally. ; This project received funding from the European Union's Horizon 2020 research and innovation programme under the Marie Sklodowska-Curie grant agreement No 702057 and the European Research Council (ERC) grant agreements no. 242658 (BIOCOM) and no. 647038 (BIODESERT). M.D.-B. is supported by a Ramón y Cajal grant from the Spanish Government (agreement no. RYC2018-025483-I) and a MUSGONET grant (LRA17\1193) from the British Ecological Society. F.T.M. also acknowledges funding from Generalitat Valenciana (CIDEGENT/2018/041) and from sDiv, the synthesis centre of the German Centre for Integrative Biodiversity Research Halle–Jena–Leipzig (iDiv). Work on microbial distribution and colonization in the B.K.S. laboratory is funded by the Australian Research Council (DP190103714). B.K.S. also acknowledges a research award by the Humboldt Foundation. C.A.G. and N.E. acknowledge support from iDiv, funded by the German Research Foundation (DFG FZT118) through flexpool proposals 34600850 and 34600844. N.E. also acknowledges support from the ERC under the European Union's Horizon 2020 research and innovation programme (grant agreement no. 677232).
10 páginas. 4 figuras.- referencias.- Supplementary data to this article can be found online at https://doi. org/10.1016/j.scitotenv.2022.153257 ; Identifying the drivers of the response of soil microbial respiration to warming is integral to accurately forecasting the carbon-climate feedbacks in terrestrial ecosystems. Microorganisms are the fundamental drivers of soil microbial respiration and its response to warming; however, the specific microbial communities and properties involved in the process remain largely undetermined. Here, we identified the associations between microbial community and temperature sensitivity (Q10) of soil microbial respiration in alpine forests along an altitudinal gradient (from 2974 to 3558 m) from the climate-sensitive Tibetan Plateau. Our results showed that changes in microbial community composition accounted for more variations of Q10 values than a wide range of other factors, including soil pH, moisture, substrate quantity and quality, microbial biomass, diversity and enzyme activities. Specifically, co-occurring microbial assemblies (i.e., ecological clusters or modules) targeting labile carbon consumption were negatively correlated with Q10 of soil microbial respiration, whereas microbial assemblies associated with recalcitrant carbon decomposition were positively correlated with Q10 of soil microbial respiration. Furthermore, there were progressive shifts of microbial assemblies from labile to recalcitrant carbon consumption along the altitudinal gradient, supporting relatively high Q10 values in high-altitude regions. Our results provide new insights into the link between changes in major microbial assemblies with different trophic strategies and Q10 of soil microbial respiration along an altitudinal gradient, highlighting that warming could have stronger effects on microbially-mediated soil organic matter decomposition in high-altitude regions than previously thought. ; This research was supported by the National Natural Science Foundation of China (32071595 and 41830756). We also thank the Fundamental Research Funds for the Central Universities (Program no. 2662019PY010 and 2662019QD055), Natural Science Fund of Hubei Province (2019CFA094), and the Strategic Priority Research Program (A) of the Chinese Academy of Sciences (Grant No. XDA20040502). We thank Hailong Li for his assistance in field sampling, and Jinhuang Lin for mapping sample locations. M.D-B. is supported by a Ramón y Cajal grant from the Spanish Government (agreement no. RYC2018-025483-I). References ; Peer reviewed
Aridity, which is increasing worldwide because of climate change, affects the structure and functioning of dryland ecosystems. Whether aridification leads to gradual (versus abrupt) and systemic (versus specific) ecosystem changes is largely unknown. We investigated how 20 structural and functional ecosystem attributes respond to aridity in global drylands. Aridification led to systemic and abrupt changes in multiple ecosystem attributes. These changes occurred sequentially in three phases characterized by abrupt decays in plant productivity, soil fertility, and plant cover and richness at aridity values of 0.54, 0.7, and 0.8, respectively. More than 20% of the terrestrial surface will cross one or several of these thresholds by 2100, which calls for immediate actions to minimize the negative impacts of aridification on essential ecosystem services for the more than 2 billion people living in drylands. ; This research was supported by the European Research Council [ERC grant nos. 242658 (BIOCOM) and 647038 (BIODESERT) awarded to F.T.M.]. M.B. acknowledges support from a Juan de la Cierva Formación grant from the Spanish Ministry of Economy and Competitiveness (FJCI-2018-036520-I). F.T.M. acknowledges support from Generalitat Valenciana (CIDEGENT/2018/041), the Alexander von Humboldt Foundation, and the Synthesis Centre for Biodiversity Sciences (sDiv) of the German Centre for Integrative Biodiversity Research (iDiv). M.D.-B. acknowledges support from the Marie Sklodowska-Curie Actions of the Horizon 2020 Framework Program H2020-MSCA-IF-2016 under REA grant no. 702057. S.S. was supported by the Spanish Government under a Ramón y Cajal contract (RYC-2016- 20604). N.G. was supported by the AgreenSkills+ fellowship program, which has received funding from the EU's Seventh Framework Programme under grant no. FP7-609398 (AgreenSkills+ contract). V.M. was supported by FRQNT-2017-NC-198009 and NSERC Discovery 2016-05716 grants from the government of Canada. H.S. was supported by a Juan de la Cierva Formación grant from the Spanish Ministry of Economy and Competitiveness (FJCI-2015-26782). A.L. and M.C.R. were supported by an ERC Advanced Grant (Gradual Change grant no. 694368) and by the Deutsche Forschungsgesellschaft (grant no. RI 1815/16-1). Y.Z. was supported by the Strategic Priority Research Program of the Chinese Academy of Sciences (grant no. XDA19030500).
Soils harbor a substantial fraction of the world's biodiversity, contributing to many crucial ecosystem functions. It is thus essential to identify general macroecological patterns related to the distribution and functioning of soil organisms to support their conservation and consideration by governance. These macroecological analyses need to represent the diversity of environmental conditions that can be found worldwide. Here we identify and characterize existing environmental gaps in soil taxa and ecosystem functioning data across soil macroecological studies and 17,186 sampling sites across the globe. These data gaps include important spatial, environmental, taxonomic, and functional gaps, and an almost complete absence of temporally explicit data. We also identify the limitations of soil macroecological studies to explore general patterns in soil biodiversity-ecosystem functioning relationships, with only 0.3% of all sampling sites having both information about biodiversity and function, although with different taxonomic groups and functions at each site. Based on this information, we provide clear priorities to support and expand soil macroecological research. ; The German Research Foundation, iDiv, the DFG and the European Research Council (ERC) under the European Union's Horizon 2020 research and innovation programme. Open access funding provided by Projekt DEAL. ; http://www.nature.com/naturecommunications ; am2021 ; Biochemistry ; Genetics ; Microbiology and Plant Pathology
Soils harbor a substantial fraction of the world's biodiversity, contributing to many crucial ecosystem functions. It is thus essential to identify general macroecological patterns related to the distribution and functioning of soil organisms to support their conservation and consideration by governance. These macroecological analyses need to represent the diversity of environmental conditions that can be found worldwide. Here we identify and characterize existing environmental gaps in soil taxa and ecosystem functioning data across soil macroecological studies and 17,186 sampling sites across the globe. These data gaps include important spatial, environmental, taxonomic, and functional gaps, and an almost complete absence of temporally explicit data. We also identify the limitations of soil macroecological studies to explore general patterns in soil biodiversity-ecosystem functioning relationships, with only 0.3% of all sampling sites having both information about biodiversity and function, although with different taxonomic groups and functions at each site. Based on this information, we provide clear priorities to support and expand soil macroecological research. ; This manuscript developed from discussions within the German Centre of Integrative Biodiversity Research funded by the German Research Foundation (DFG FZT118). CAG and NE acknowledge funding by iDiv (DFG FZT118) Flexpool proposal 34600850. C.A.G., A.H.B., J.S., A.C., N.G.R., S.C., L.B., M.C.R., F.B., J.O., G.P., H.R.P.P., M.W., T.W., K.K., and N.E. acknowledge funding by iDiv (DFG FZT118) Flexpool proposal 34600844. N.E. acknowledges funding by the DFG (FOR 1451) and the European Research Council (ERC) under the European Union's Horizon 2020 research and innovation programme (grant agreement no. 677232). Finally we would like to acknowledge the contribution of all the authors that provided their datasets for analysis within this paper. Open access funding provided by Projekt DEAL.
The role of soil biodiversity in regulating multiple ecosystem functions is poorly understood, limiting our ability to predict how soil biodiversity loss might affect human wellbeing and ecosystem sustainability. Here, combining a global observational study with an experimental microcosm study, we provide evidence that soil biodiversity (bacteria, fungi, protists and invertebrates) is significantly and positively associated with multiple ecosystem functions. These functions include nutrient cycling, decomposition, plant production, and reduced potential for pathogenicity and belowground biological warfare. Our findings also reveal the context dependency of such relationships and the importance of the connectedness, biodiversity and nature of the globally distributed dominant phylotypes within the soil network in maintaining multiple functions. Moreover, our results suggest that the positive association between plant diversity and multifunctionality across biomes is indirectly driven by soil biodiversity. Together, our results provide insights into the importance of soil biodiversity for maintaining soil functionality locally and across biomes, as well as providing strong support for the inclusion of soil biodiversity in conservation and management programmes. Combining field data from 83 sites on five continents, together with microcosm experiments, the authors show that nutrient cycling, decomposition, plant production and other ecosystem functions are positively associated with a higher diversity of a wide range of soil organisms. ; Marie Sklodowska-Curie ; We thank N. Fierer, M. Gebert, J. Henley, V. Ochoa, F. T. Maestre and B. Gozalo for their help with laboratory analyses; O. Sala, C. Siebe, C. Currier, M. A. Bowker, V. Parry, H. Lambers, P. Vitousek, V. M. Pena-Ramirez, L. Riedel, J. Larson, K. Waechter, W. Williams, S. Williams, B. Sulman, D. Buckner and B. Anacker for their help with soil sampling in Colorado, Hawaii, Iceland, New Mexico, Arizona, Mexico and Australia; the City of Boulder Open Space and Mountain Parks for allowing us to conduct these samplings; C. Cano-Diaz for her advice about R analyses; S. K. Travers for her help with mapping. This project has received funding from the European Union's Horizon 2020 research and innovation programme under the Marie Sklodowska-Curie grant agreement no. 702057. M.D.-B. is supported by the Spanish Government under a Ramon y Cajal contract RYC2018-025483-I. This research is supported by the Australian Research Council projects (DP170104634; DP190103714). S.A. and F.D.A. are funded by FONDECYT 1170995, IAI-CRN 3005, PFB-23 (from CONICYT) and P05-002 (from Millennium Scientific Initiative). N.A.C. acknowledges support from Churchill College, University of Cambridge; and M.A.W. from the Wilderness State Park, Michigan for access to sample soil and conduct ecosystem survey. B.K.S. acknowledges a research award from the Humboldt Foundation. J.-Z.H. acknowledges support from the Australia Research Council (project DP170103628); and A.G. from the Spanish Ministry (project CGL2017-88124-R). F.B. thanks the Spanish Ministry and FEDER funds for the CICYT project AGL2017-85755-R, the CSIC project 201740I008 and funds from 'Fundacion Seneca' from Murcia Province (19896/GERM/15). P.T. thanks K. Little for her help with laboratory analyses. S.C.R. was supported by the US Geological Survey Ecosystems Mission Area. Any use of trade, firm or product names is for descriptive purposes only and does not imply endorsement by the US Government. S.N. was funded by the Austrian Science Fund (grant Y801-B16). ; Public domain authored by a U.S. government employee
Identifying the global drivers of soil priming is essential to understanding C cycling in terrestrial ecosystems. We conducted a survey of soils across 86 globally-distributed locations, spanning a wide range of climates, biotic communities, and soil conditions, and evaluated the apparent soil priming effect using C-13-glucose labeling. Here we show that the magnitude of the positive apparent priming effect (increase in CO2 release through accelerated microbial biomass turnover) was negatively associated with SOC content and microbial respiration rates. Our statistical modeling suggests that apparent priming effects tend to be negative in more mesic sites associated with higher SOC contents. In contrast, a single-input of labile C causes positive apparent priming effects in more arid locations with low SOC contents. Our results provide solid evidence that SOC content plays a critical role in regulating apparent priming effects, with important implications for the improvement of C cycling models under global change scenarios. ; European UnionEuropean Union (EU) [702057]; FEDER fundsEuropean Union (EU) [AGL2017-85755-R]; CSICConsejo Superior de Investigaciones Cientificas (CSIC) [201740I008]; I-LINK + 2018 [LINKA20069]; "Fundacion Seneca" from Murcia Province [19896/GERM/15]; Marie Sklodowska-Curie Actions of the Horizon 2020 Framework Programme H2020-MSCA-IF-2016 under REA grant [702057]; FONDECYTComision Nacional de Investigacion Cientifica y Tecnologica (CONICYT)CONICYT FONDECYT [1170995]; IAI-CRN [3005]; CONICYTComision Nacional de Investigacion Cientifica y Tecnologica (CONICYT) [PFB-23]; Millennium Scientific Initiative [P05-002]; Churchill College (University of Cambridge); Department of Energy Terrestrial Ecosystem Sciences Program [DESC-0008168]; USGS Ecosystems Mission Area; EPA-STAR Graduate FellowshipUnited States Environmental Protection Agency [U-916251]; Merriam-Powell Center for Environmental Research Graduate Fellowship; Achievement Rewards for College Scientists (ARCS) Foundation of Arizona Scholarship; McIntire-Stennis appropriations ; This project has received funding from the European Union's Horizon 2020 research and innovation programme under the Marie Sklodowska-Curie grant agreement No 702057. F.B., J.L., A.V., C.G., T.H. thank the Spanish Ministry and FEDER funds for the CICYT project AGL2017-85755-R, the CSIC projects 201740I008 and I-LINK + 2018 (LINKA20069), and funds from "Fundacion Seneca" from Murcia Province (19896/GERM/15). M.D-B. acknowledges support from the Marie Sklodowska-Curie Actions of the Horizon 2020 Framework Programme H2020-MSCA-IF-2016 under REA grant agreement no 702057. S.A and F.D.A were supported by FONDECYT 1170995. C.A.P is grateful to IAI-CRN 3005. C.A.P and F.D.A were supported by PFB-23 (from CONICYT) and P05-002 (from Millennium Scientific Initiative) to the Institute of Ecology and Biodiversity, Chile. N.A.C is grateful to Churchill College (University of Cambridge) for financial support and to Dr. Vicki Parry for fieldwork assistance. S.R acknowledges support from the Department of Energy Terrestrial Ecosystem Sciences Program (DESC-0008168) and the USGS Ecosystems Mission Area. A.A.B. and F.S. acknowledge support from Jennifer Harden and Sebastian Doetterl for prior works and information about sites along the Merced Chronosequence and from Benjamin Sulman for help during sampling. The Arizona research sites were established with the support of an EPA-STAR Graduate Fellowship (U-916251), a Merriam-Powell Center for Environmental Research Graduate Fellowship, an Achievement Rewards for College Scientists (ARCS) Foundation of Arizona Scholarship, and McIntire-Stennis appropriations to Northern Arizona University and the State of Arizona. Any use of trade, firm, or product names is for descriptive purposes only and does not imply endorsement by the U.S. Government.
The importance of soil age as an ecosystem driver across biomes remains largely unresolved. By combining a cross-biome global field survey, including data for 32 soil, plant, and microbial properties in 16 soil chronosequences, with a global meta-analysis, we show that soil age is a significant ecosystem driver, but only accounts for a relatively small proportion of the cross-biome variation in multiple ecosystem properties. Parent material, climate, vegetation and topography predict, collectively, 24 times more variation in ecosystem properties than soil age alone. Soil age is an important local-scale ecosystem driver; however, environmental context, rather than soil age, determines the rates and trajectories of ecosystem development in structure and function across biomes. Our work provides insights into the natural history of terrestrial ecosystems. We propose that, regardless of soil age, changes in the environmental context, such as those associated with global climatic and land-use changes, will have important long-term impacts on the structure and function of terrestrial ecosystems across biomes. ; This project received funding from the European Union's Horizon 2020 research and innovation program under the Marie Sklodowska-Curie Grant Agreement No. 702057 (CLIMIFUN). M.D.-B. is supported by a Ramón y Cajal grant from the Spanish Ministry of Science and Innovation (RYC2018-025483-I), and by the BES Grant Agreement No. LRB17\1019 (MUSGONET). F.B. is grateful to the Spanish Ministry and FEDER funds for the project AGL2017–85755-R, the i-LINK+2018 (LINKA20069) from CSIC, and received funds from "Fundación Séneca" from Murcia Province (19896/GERM/15). S.R. was supported by the US Geological Survey Ecosystems Mission Area. C.P. acknowledges support from the Spanish State Plan for Scientific and Technical Research and Innovation (2013–2016), award ref. AGL201675762-R (AEI/FEDER, UE). A.G. acknowledges support from the Spanish Ministry of Science (CGL2017-88124-R). F.A. is supported by FONDECYT 11180538 and S.A. by FONDECYT 1170995. We would like to thank Peter Vitousek for his comments on a previous draft of this paper. Moreover, we thank Matt Gebert, Jessica Henley, Fernando T. Maestre, Victoria Ochoa, and Beatriz Gozalo for their help with lab analyses, and Emilio Guirado for his advice with topographic analyses. We also want to thank Osvaldo Sala, Matthew A. Bowker, Peter Vitousek, Courtney Currier, Martin Kirchmair, Victor M. Peña-Ramírez, Lynn Riedel, Julie Larson, Katy Waechter, David Buckner, and Brian Anacker for their help with soil sampling, and to the City of Boulder Open Space and Mountain Parks for allowing us to conduct these samplings. We are also grateful to the Division of Forestry and Wildlife of the State of Hawai'i and Koke'e State Park for their logistical assistance and for allowing us access to the HA sites. The Arizona research sites were established with the support of an EPA‐STAR Graduate Fellowship (U‐916251), a Merriam‐Powell Center for Environmental Research Graduate Fellowship, an Achievement Rewards for College Scientists (ARCS) Foundation of Arizona Scholarship, and McIntire‐Stennis appropriations to Northern Arizona University and the State of Arizona. Any use of trade, product, or firm names is for descriptive purposes only and does not imply endorsement by the U.S. Government.
The importance of soil age as an ecosystem driver across biomes remains largely unresolved. By combining a cross-biome global field survey, including data for 32 soil, plant, and microbial properties in 16 soil chronosequences, with a global meta-analysis, we show that soil age is a significant ecosystem driver, but only accounts for a relatively small proportion of the cross-biome variation in multiple ecosystem properties. Parent material, climate, vegetation and topography predict, collectively, 24 times more variation in ecosystem properties than soil age alone. Soil age is an important local-scale ecosystem driver; however, environmental context, rather than soil age, determines the rates and trajectories of ecosystem development in structure and function across biomes. Our work provides insights into the natural history of terrestrial ecosystems. We propose that, regardless of soil age, changes in the environmental context, such as those associated with global climatic and land-use changes, will have important long-term impacts on the structure and function of terrestrial ecosystems across biomes. ; This project received funding from the European Union's Horizon 2020 research and innovation program under the Marie Sklodowska-Curie Grant Agreement No. 702057 (CLIMIFUN). M.D.-B. is supported by a Ramón y Cajal grant from the Spanish Ministry of Science and Innovation (RYC2018-025483-I), and by the BES Grant Agreement No. LRB17\1019 (MUSGONET). F.B. is grateful to the Spanish Ministry and FEDER funds for the project AGL2017–85755-R, the i-LINK+2018 (LINKA20069) from CSIC, and received funds from "Fundación Séneca" from Murcia Province (19896/GERM/15). S.R. was supported by the US Geological Survey Ecosystems Mission Area. C.P. acknowledges support from the Spanish State Plan for Scientific and Technical Research and Innovation (2013–2016), award ref. AGL201675762-R (AEI/FEDER, UE). A.G. acknowledges support from the Spanish Ministry of Science (CGL2017-88124-R). F.A. is supported by FONDECYT 11180538 and S.A. by FONDECYT 1170995. We would like to thank Peter Vitousek for his comments on a previous draft of this paper. Moreover, we thank Matt Gebert, Jessica Henley, Fernando T. Maestre, Victoria Ochoa, and Beatriz Gozalo for their help with lab analyses, and Emilio Guirado for his advice with topographic analyses. We also want to thank Osvaldo Sala, Matthew A. Bowker, Peter Vitousek, Courtney Currier, Martin Kirchmair, Victor M. Peña-Ramírez, Lynn Riedel, Julie Larson, Katy Waechter, David Buckner, and Brian Anacker for their help with soil sampling, and to the City of Boulder Open Space and Mountain Parks for allowing us to conduct these samplings. We are also grateful to the Division of Forestry and Wildlife of the State of Hawai'i and Koke'e State Park for their logistical assistance and for allowing us access to the HA sites. The Arizona research sites were established with the support of an EPA‐STAR Graduate Fellowship (U‐916251), a Merriam‐Powell Center for Environmental Research Graduate Fellowship, an Achievement Rewards for College Scientists (ARCS) Foundation of Arizona Scholarship, and McIntire‐Stennis appropriations to Northern Arizona University and the State of Arizona. Any use of trade, product, or firm names is for descriptive purposes only and does not imply endorsement by the U.S. Government.
The importance of soil age as an ecosystem driver across biomes remains largely unresolved. By combining a cross-biome global field survey, including data for 32 soil, plant, and microbial properties in 16 soil chronosequences, with a global meta-analysis, we show that soil age is a significant ecosystem driver, but only accounts for a relatively small proportion of the cross-biome variation in multiple ecosystem properties. Parent material, climate, vegetation and topography predict, collectively, 24 times more variation in ecosystem properties than soil age alone. Soil age is an important local-scale ecosystem driver; however, environmental context, rather than soil age, determines the rates and trajectories of ecosystem development in structure and function across biomes. Our work provides insights into the natural history of terrestrial ecosystems. We propose that, regardless of soil age, changes in the environmental context, such as those associated with global climatic and land-use changes, will have important long-term impacts on the structure and function of terrestrial ecosystems across biomes. Soil age is thought to be an important driver of ecosystem development. Here, the authors perform a global survey of soil chronosequences and meta-analysis to show that, contrary to expectations, soil age is a relatively minor ecosystem driver at the biome scale once other drivers such as parent material, climate, and vegetation type are accounted for. ; European Union's Horizon 2020 research and innovation program under the Marie Sklodowska-Curie GrantEuropean Union (EU) [702057]; Ramon y Cajal grant from the Spanish Ministry of Science and Innovation [RYC2018-025483-I]; BES Grant [LRB17\1019]; Spanish MinistrySpanish Government; FEDER fundsEuropean Union (EU) [AGL2017-85755-R]; i-LINK+2018 from CSIC [LINKA20069]; Fundacion Seneca" from Murcia Province [19896/GERM/15]; US Geological Survey Ecosystems Mission Area; Spanish State Plan for Scientific and Technical Research and Innovation (2013-2016) [AGL201675762-R]; Spanish Ministry of ScienceSpanish Government [CGL2017-88124-R]; FONDECYTComision Nacional de Investigacion Cientifica y Tecnologica (CONICYT)CONICYT FONDECYT [1170995, 11180538]; EPASTAR Graduate FellowshipUnited States Environmental Protection Agency [U-916251]; Merriam-Powell Center for Environmental Research Graduate Fellowship; Achievement Rewards for College Scientists (ARCS) Foundation of Arizona Scholarship; McIntire-Stennis appropriations to Northern Arizona University; State of Arizona ; This project received funding from the European Union's Horizon 2020 research and innovation program under the Marie Sklodowska-Curie Grant Agreement No. 702057 (CLIMIFUN). M.D.-B. is supported by a Ramon y Cajal grant from the Spanish Ministry of Science and Innovation (RYC2018-025483-I), and by the BES Grant Agreement No. LRB17\1019 (MUSGONET). F.B. is grateful to the Spanish Ministry and FEDER funds for the project AGL2017-85755-R, the i-LINK+2018 (LINKA20069) from CSIC, and received funds from "Fundacion Seneca" from Murcia Province (19896/GERM/15). S.R. was supported by the US Geological Survey Ecosystems Mission Area. C.P. acknowledges support from the Spanish State Plan for Scientific and Technical Research and Innovation (2013-2016), award ref. AGL201675762-R (AEI/FEDER, UE). A.G. acknowledges support from the Spanish Ministry of Science (CGL2017-88124-R). F.A. is supported by FONDECYT 11180538 and S.A. by FONDECYT 1170995. We would like to thank Peter Vitousek for his comments on a previous draft of this paper. Moreover, we thank Matt Gebert, Jessica Henley, Fernando T. Maestre, Victoria Ochoa, and Beatriz Gozalo for their help with lab analyses, and Emilio Guirado for his advice with topographic analyses. We also want to thank Osvaldo Sala, Matthew A. Bowker, Peter Vitousek, Courtney Currier, Martin Kirchmair, Victor M. Pena-Ramirez, Lynn Riedel, Julie Larson, Katy Waechter, David Buckner, and Brian Anacker for their help with soil sampling, and to the City of Boulder Open Space and Mountain Parks for allowing us to conduct these samplings. We are also grateful to the Division of Forestry and Wildlife of the State of Hawai'i and Koke'e State Park for their logistical assistance and for allowing us access to the HA sites. The Arizona research sites were established with the support of an EPASTAR Graduate Fellowship (U-916251), a Merriam-Powell Center for Environmental Research Graduate Fellowship, an Achievement Rewards for College Scientists (ARCS) Foundation of Arizona Scholarship, and McIntire-Stennis appropriations to Northern Arizona University and the State of Arizona. Any use of trade, product, or firm names is for descriptive purposes only and does not imply endorsement by the U.S. Government.
