Forest carbon stocks increase with higher dominance of ectomycorrhizal trees in high latitude forests.
Journal
Nature communications
ISSN: 2041-1723
Titre abrégé: Nat Commun
Pays: England
ID NLM: 101528555
Informations de publication
Date de publication:
16 Jul 2024
16 Jul 2024
Historique:
received:
01
12
2023
accepted:
10
07
2024
medline:
16
7
2024
pubmed:
16
7
2024
entrez:
15
7
2024
Statut:
epublish
Résumé
Understanding the mechanisms controlling forest carbon accumulation is crucial for predicting and mitigating future climate change. Yet, it remains unclear whether the dominance of ectomycorrhizal (EcM) trees influences the carbon accumulation of entire forests. In this study, we analyzed forest inventory data from over 4000 forest plots across Northeast China. We find that EcM tree dominance consistently exerts a positive effect on tree, soil, and forest carbon stocks. Moreover, we observe that these positive effects are more pronounced during unfavorable climate conditions, at lower tree species richness, and during early successional stages. This underscores the potential of increasing the dominance of native EcM tree species not only to enhance carbon stocks but also to bolster resilience against climate change in high-latitude forests. Here we show that forest managers can make informed decisions to optimize carbon accumulation by considering various factors such as mycorrhizal types, climate, successional stages, and species richness.
Identifiants
pubmed: 39009629
doi: 10.1038/s41467-024-50423-9
pii: 10.1038/s41467-024-50423-9
doi:
Substances chimiques
Carbon
7440-44-0
Soil
0
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
5959Informations de copyright
© 2024. The Author(s).
Références
Bonan, G. B. Forests and climate change: Forcings, feedbacks, and the climate benefits of forests. Science 320, 1444–1449 (2008).
pubmed: 18556546
doi: 10.1126/science.1155121
Pan, Y. et al. A large and persistent carbon sink in the world’s forests. Science 333, 988–993 (2011).
pubmed: 21764754
doi: 10.1126/science.1201609
Beer, C. et al. Terrestrial gross carbon dioxide uptake: global distribution and covariation with climate. Science 329, 834–838 (2010).
pubmed: 20603496
doi: 10.1126/science.1184984
Rockström, J. et al. We need biosphere stewardship that protects carbon sinks and builds resilience. Proc. Natl. Acad. Sci. USA. 118, e2115218118 (2021).
pubmed: 34526406
pmcid: 8463783
doi: 10.1073/pnas.2115218118
Wu, C. et al. Uncertainty in US forest carbon storage potential due to climate risks. Nat. Geosci. 16, 422–429 (2023).
doi: 10.1038/s41561-023-01166-7
Zhang, T. et al. Shifts in tree functional composition amplify the response of forest biomass to climate. Nature 556, 99–102 (2018).
pubmed: 29562235
doi: 10.1038/nature26152
Bongers, F. J. et al. Functional diversity effects on productivity increase with age in a forest biodiversity experiment. Nat. Ecol. Evol. 5, 1594–1603 (2021).
pubmed: 34737435
doi: 10.1038/s41559-021-01564-3
Chen, X. et al. Tree diversity increases decadal forest soil carbon and nitrogen accrual. Nature 618, 94–101 (2023).
pubmed: 37100916
doi: 10.1038/s41586-023-05941-9
De Deyn, G. B. et al. Plant functional traits and soil carbon sequestration in contrasting biomes. Ecol. Lett. 11, 516–531 (2008).
pubmed: 18279352
doi: 10.1111/j.1461-0248.2008.01164.x
Augusto, L. et al. Tree functional traits, forest biomass, and tree species diversity interact with site properties to drive forest soil carbon. Nat. Commun. 13, 1097 (2022).
pubmed: 35233020
pmcid: 8888738
doi: 10.1038/s41467-022-28748-0
Luo, S. et al. Higher productivity in forests with mixed mycorrhizal strategies. Nat. Commun. 14, 1377 (2023).
pubmed: 36914630
pmcid: 10011551
doi: 10.1038/s41467-023-36888-0
Jo, I. et al. Shifts in dominant tree mycorrhizal associations in response to anthropogenic impacts. Sci. Adv. 5, eaav6358 (2019).
pubmed: 30989116
pmcid: 6457943
doi: 10.1126/sciadv.aav6358
Genre, A. et al. Unique and common traits in mycorrhizal symbioses. Nat. Rev. Microbiol. 18, 649–660 (2020).
pubmed: 32694620
doi: 10.1038/s41579-020-0402-3
Phillips, R. P. et al. The mycorrhizal‐associated nutrient economy: a new framework for predicting carbon–nutrient couplings in temperate forests. New Phytol. 199, 41–51 (2013).
pubmed: 23713553
doi: 10.1111/nph.12221
Averill, C. et al. Mycorrhiza-mediated competition between plants and decomposers drives soil carbon storage. Nature 505, 543–545 (2014).
pubmed: 24402225
doi: 10.1038/nature12901
Steidinger, B. S. et al. Climatic controls of decomposition drive the global biogeography of forest-tree symbioses. Nature 569, 404–408 (2019).
pubmed: 31092941
doi: 10.1038/s41586-019-1128-0
Tang, B. et al. Arbuscular mycorrhizal fungi benefit plants in response to major global change factors. Ecol. Lett. 26, 2087–2097 (2023).
pubmed: 37794719
doi: 10.1111/ele.14320
Chen, L. et al. Differential soil fungus accumulation and density dependence of trees in a subtropical forest. Science 366, 124–128 (2019).
pubmed: 31604314
doi: 10.1126/science.aau1361
Carteron, A. et al. Mycorrhizal dominance reduces local tree species diversity across US forests. Nat. Ecol. Evol. 6, 370–374 (2022).
pubmed: 35210575
doi: 10.1038/s41559-021-01634-6
Lindahl, B. D. & Tunlid, A. Ectomycorrhizal fungi-potential organic matter decomposers, yet not saprotrophs. New Phytol. 205, 1443–1447 (2015).
pubmed: 25524234
doi: 10.1111/nph.13201
Hodge, A. et al. An arbuscular mycorrhizal fungus accelerates decomposition and acquires nitrogen directly from organic material. Nature 413, 297–299 (2001).
pubmed: 11565029
doi: 10.1038/35095041
Shao, S. et al. Ectomycorrhizal effects on decomposition are highly dependent on fungal traits, climate, and litter properties: A model-based assessment. Soil Biol. Biochem. 184, 109073 (2023).
doi: 10.1016/j.soilbio.2023.109073
Read, D. J. et al. Mycorrhizas and nutrient cycling in ecosystems-a journey towards relevance? New phytol. 157, 475–492 (2003).
pubmed: 33873410
doi: 10.1046/j.1469-8137.2003.00704.x
Orwin, K. H. et al. Organic nutrient uptake by mycorrhizal fungi enhances ecosystem carbon storage: a model‐based assessment. Ecol. Lett. 14, 493–502 (2011).
pubmed: 21395963
doi: 10.1111/j.1461-0248.2011.01611.x
Hicks Pries, C. E. et al. Differences in soil organic matter between EcM‐and AM‐dominated forests depend on tree and fungal identity. Ecology 104, e3929 (2023).
pubmed: 36424763
doi: 10.1002/ecy.3929
Cotrufo, M. F. et al. Soil carbon storage informed by particulate and mineral-associated organic matter. Nat. Geosci. 12, 989–994 (2019).
doi: 10.1038/s41561-019-0484-6
Anthony, M. A. et al. Forest tree growth is linked to mycorrhizal fungal composition and function across Europe. ISME J. 16, 1327–1336 (2022).
pubmed: 35001085
pmcid: 9038731
doi: 10.1038/s41396-021-01159-7
Tedersoo, L. et al. How mycorrhizal associations drive plant population and community biology. Science 367, eaba1223 (2020).
pubmed: 32079744
doi: 10.1126/science.aba1223
Anderson‐Teixeira, K. J. et al. Altered dynamics of forest recovery under a changing climate. Global Change Biol. 19, 2001–2021 (2013).
doi: 10.1111/gcb.12194
Pastor, J. et al. Influence of climate, soil moisture, and succession on forest carbon and nitrogen cycles. Biogeochemistry 2, 3–27 (1986).
doi: 10.1007/BF02186962
Yan, G. et al. Climate and mycorrhizae mediate the relationship of tree species diversity and carbon stocks in subtropical forests. J. Ecol. 110, 2462–2474 (2022).
doi: 10.1111/1365-2745.13962
Bennett, A. E. et al. Climate change influences mycorrhizal fungal-plant interactions, but conclusions are limited by geographical study bias. Ecology 101, e02978 (2020).
pubmed: 31953955
doi: 10.1002/ecy.2978
Liu, R. et al. Mycorrhizal effects on decomposition and soil CO
doi: 10.1111/1365-2745.13770
Yan, G. et al. Assembly processes, driving factors, and shifts in soil microbial communities across secondary forest succession. Land Degrad. Dev. 34, 3130–3143 (2023).
doi: 10.1002/ldr.4671
Chang, C. C. & Turner, B. L. Ecological succession in a changing world. J. Ecol. 107, 503–509 (2019).
doi: 10.1111/1365-2745.13132
Fichtner, A. et al. From competition to facilitation: how tree species respond to neighbourhood diversity. Ecol. Lett. 20, 892–900 (2017).
pubmed: 28616871
doi: 10.1111/ele.12786
Schnabel, F. et al. Species richness stabilizes productivity via asynchrony and drought-tolerance diversity in a large-scale tree biodiversity experiment. Sci. Adv. 7, eabk1643 (2021).
pubmed: 34919425
pmcid: 8682986
doi: 10.1126/sciadv.abk1643
Cheng, L. et al. Mycorrhizal fungi and roots are complementary in foraging within nutrient patches. Ecology 97, 2815–2823 (2016).
pubmed: 27859112
doi: 10.1002/ecy.1514
Augusto, L. et al. Soil parent material-A major driver of plant nutrient limitations in terrestrial ecosystems. Global Change Biol. 23, 3808–3824 (2017).
doi: 10.1111/gcb.13691
Simard, S. W. et al. Net transfer of carbon between ectomycorrhizal tree species in the field. Nature 388, 579–582 (1997).
doi: 10.1038/41557
van Der Heijden, M. G. et al. Mycorrhizal ecology and evolution: the past, the present, and the future. New phytol. 205, 1406–1423 (2015).
pubmed: 25639293
doi: 10.1111/nph.13288
Liang, M. et al. Soil fungal networks maintain local dominance of ectomycorrhizal trees. Nat. Commun. 11, 2636 (2020).
pubmed: 32457288
pmcid: 7250933
doi: 10.1038/s41467-020-16507-y
Jacobs, L. M. et al. Interactions among decaying leaf litter, root litter and soil organic matter vary with mycorrhizal type. J. Ecol. 106, 502–513 (2018).
doi: 10.1111/1365-2745.12921
Dunleavy, H. R. et al. Long-term experimental warming and fertilization have opposing effects on ectomycorrhizal root enzyme activity and fungal community composition in Arctic tundra. Soil Biol. Biochem. 154, 108151 (2021).
doi: 10.1016/j.soilbio.2021.108151
Li, S. et al. Effects of plant diversity and soil properties on soil fungal community structure with secondary succession in the Pinus yunnanensis forest. Geoderma 379, 114646 (2020).
doi: 10.1016/j.geoderma.2020.114646
Yan, G. et al. Nitrogen deposition and decreased precipitation altered nutrient foraging strategies of three temperate trees by affecting root and mycorrhizal traits. Catena 181, 104094 (2019).
doi: 10.1016/j.catena.2019.104094
Jiang, S. et al. Changes in soil bacterial and fungal community composition and functional groups during the succession of boreal forests. Soil Biol. Biochem. 161, 108393 (2021).
doi: 10.1016/j.soilbio.2021.108393
Koziol, L. & Bever, J. D. Mycorrhizal feedbacks generate positive frequency dependence accelerating grassland succession. J. Ecol. 107, 622–632 (2019).
doi: 10.1111/1365-2745.13063
Huang, Y. et al. Impacts of species richness on productivity in a large-scale subtropical forest experiment. Science 362, 80–83 (2018).
pubmed: 30287660
doi: 10.1126/science.aat6405
Pellissier, V. et al. Niche packing and expansion account for species richness-productivity relationships in global bird assemblages. Global Ecol. Biogeogr. 27, 604–615 (2018).
doi: 10.1111/geb.12723
Conti, G. & Díaz, S. Plant functional diversity and carbon storage-an empirical test in semi‐arid forest ecosystems. J. Ecol. 101, 18–28 (2013).
doi: 10.1111/1365-2745.12012
Patoine, G. et al. Tree litter functional diversity and nitrogen concentration enhance litter decomposition via changes in earthworm communities. Ecol. Evol. 10, 6752–6768 (2020).
pubmed: 32724548
pmcid: 7381558
doi: 10.1002/ece3.6474
Odum, E. P. The strategy of ecosystem development: An understanding of ecological succession provides a basis for resolving man’s conflict with nature. Science 164, 262–270 (1969).
pubmed: 5776636
doi: 10.1126/science.164.3877.262
Curtis, J. T. et al. An upland forest continuum in the prairie-forest border region of Wisconsin. Ecology 32, 476–496 (1951).
doi: 10.2307/1931725
Mainali, K. P. et al. A better index for analysis of co-occurrence and similarity. Sci. Adv. 8, eabj9204 (2022).
pubmed: 35080967
doi: 10.1126/sciadv.abj9204
CMEP. The National Ecological Protection Red Line-technical guidelines for the delineation of ecological functions red line (trial) (In Chinese). (No. 2014.1). Chinese Ministry of Environmental Protection, Beijing, China (2014).
Kunstler, G. et al. Plant functional traits have globally consistent effects on competition. Nature 529, 204–207 (2016).
pubmed: 26700807
doi: 10.1038/nature16476
Reich, P. B. et al. From tropics to tundra: Global convergence in plant functioning. Proc. Natl. Acad. Sci. USA. 94, 13730–13734 (1997).
pubmed: 9391094
pmcid: 28374
doi: 10.1073/pnas.94.25.13730
Kattge, J. et al. TRY-a global database of plant traits. Global Change Biol. 17, 2905–2935 (2011).
doi: 10.1111/j.1365-2486.2011.02451.x
Wang, H. et al. The China plant trait database version 2. Sci. Data 9, 769 (2022).
pubmed: 36522346
pmcid: 9755148
doi: 10.1038/s41597-022-01884-4
Tang, X. et al. Carbon pools in China’s terrestrial ecosystems: New estimates based on an intensive field survey. P. Natl. Acad. Sci. USA. 115, 4021–4026 (2018).
doi: 10.1073/pnas.1700291115
Liu, X. et al. Tree species richness increases ecosystem carbon storage in subtropical forests. Proc. Roy. Soc. B. 285, 20181240 (2018).
doi: 10.1098/rspb.2018.1240
Li, Y. et al. Drivers of tree carbon storage in subtropical forests. Sci. Total. Environ. 654, 684–693 (2019).
pubmed: 30448659
doi: 10.1016/j.scitotenv.2018.11.024
Soudzilovskaia, N. A. et al. FungalRoot: Global online database of plant mycorrhizal associations. New Phytol. 227, 955–966 (2020).
pubmed: 32239516
doi: 10.1111/nph.16569
Bolyen, E. et al. Reproducible, interactive, scalable and extensible microbiome data science using QIIME 2. Nat. Biotechnol. 37, 852–857 (2019).
pubmed: 31341288
pmcid: 7015180
doi: 10.1038/s41587-019-0209-9
Nilsson, R. H. et al. The UNITE database for molecular identification of fungi: handling dark taxa and parallel taxonomic classifications. Nucleic Acids Res. 47, D259–D264 (2019).
pubmed: 30371820
doi: 10.1093/nar/gky1022
Oliver, A. K. et al. Polymerase matters: non-proofreading enzymes inflate fungal community richness estimates by up to 15%. Fungal Ecol. 15, 86–89 (2015).
doi: 10.1016/j.funeco.2015.03.003
Nguyen, N. H. et al. FUNGuild: An open annotation tool for parsing fungal community datasets by ecological guild. Fungal Ecol. 20, 241–248 (2016).
doi: 10.1016/j.funeco.2015.06.006
Smithson, M. et al. A better lemon squeezer? Maximum-likelihood regression with beta-distributed dependent variables. Psychol. Methods 11, 54 (2006).
pubmed: 16594767
doi: 10.1037/1082-989X.11.1.54
Averill, C. et al. Continental‐scale nitrogen pollution is shifting forest mycorrhizal associations and soil carbon stocks. Global Change Biol. 24, 4544–4553 (2018).
doi: 10.1111/gcb.14368
Liaw, A. et al. Classification and regression by randomForest. R news 2, 18–22 (2002).
Van Der Heijden, M. G. et al. Mycorrhizal fungal diversity determines plant biodiversity, ecosystem variability and productivity. Nature 396, 69–72 (1998).
doi: 10.1038/23932
Lefcheck, J. S. piecewiseSEM: Piecewise structural equation modelling in r for ecology, evolution, and systematics. Methods Ecol. Evol. 7, 573–579 (2016).
doi: 10.1111/2041-210X.12512