Unexpected sustained soil carbon flux in response to simultaneous warming and nitrogen enrichment compared with single factors alone.


Journal

Nature ecology & evolution
ISSN: 2397-334X
Titre abrégé: Nat Ecol Evol
Pays: England
ID NLM: 101698577

Informations de publication

Date de publication:
24 Sep 2024
Historique:
received: 26 07 2023
accepted: 23 08 2024
medline: 25 9 2024
pubmed: 25 9 2024
entrez: 24 9 2024
Statut: aheadofprint

Résumé

Recent observations document that long-term soil warming in a temperate deciduous forest leads to significant soil carbon loss, whereas chronic soil nitrogen enrichment leads to significant soil carbon gain. Most global change experiments like these are single factor, investigating the impacts of one stressor in isolation of others. Because warming and ecosystem nitrogen enrichment are happening concurrently in many parts of the world, we designed a field experiment to test how these two factors, alone and in combination, impact soil carbon cycling. Here, we show that long-term continuous soil warming or nitrogen enrichment when applied alone followed the predicted response, with warming resulting in significant soil carbon loss and nitrogen fertilization tending towards soil carbon gain. The combination treatment showed an unanticipated response, whereby soil respiratory carbon loss was significantly higher than either single factor alone, but without a concomitant decline in soil carbon storage. Observations suggest that when soils are exposed to both factors simultaneously, plant carbon inputs to the soil are enhanced, counterbalancing soil carbon loss and helping maintain soil carbon stocks near control levels. This has implications for both atmospheric CO

Identifiants

pubmed: 39317790
doi: 10.1038/s41559-024-02546-x
pii: 10.1038/s41559-024-02546-x
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© 2024. The Author(s), under exclusive licence to Springer Nature Limited.

Références

Song, J. et al. A meta-analysis of 1,119 manipulative experiments on terrestrial carbon-cycling responses to global change. Nat. Ecol. Evol. 3, 1309–1320 (2019).
doi: 10.1038/s41559-019-0958-3 pubmed: 31427733
Rillig, M. C. et al. The role of multiple global change factors in driving soil functions and microbial biodiversity. Science 366, 886–890 (2019).
doi: 10.1126/science.aay2832 pubmed: 31727838 pmcid: 6941939
Georgiou, K. et al. Global stocks and capacity of mineral-associated soil organic carbon. Nat. Commun. 13, 3797 (2022).
doi: 10.1038/s41467-022-31540-9 pubmed: 35778395 pmcid: 9249731
Pan, Y. et al. A large and persistent carbon sink in the world’s forests. Science 333, 988–993 (2011).
doi: 10.1126/science.1201609 pubmed: 21764754
IPCC. Climate Change 2023: Synthesis Report. A Contribution of Working Groups I, II and III to the Sixth Assessment Report of the Intergovernmental Panel on Climate Change (eds Core Writing Team, Lee, H. & Romero, J.) 35–115 (IPCC, 2023).
Decina, S. M., Hutyra, L. R. & Templer, P. H. Hotspots of nitrogen deposition in the world’s urban areas: a global data synthesis. Front. Ecol. Environ. 18, 92–100 (2019).
doi: 10.1002/fee.2143
Zhou, Z., Wang, C. & Luo, Y. Meta-analysis of the impacts of global change factors on soil microbial diversity and functionality. Nat. Commun. 11, 3072 (2020).
doi: 10.1038/s41467-020-16881-7 pubmed: 32555185 pmcid: 7300008
Melillo, J. M. et al. Long-term pattern and magnitude of soil carbon feedback to the climate system in a warming world. Science 358, 101–105 (2017).
doi: 10.1126/science.aan2874 pubmed: 28983050
Soong, J. L. et al. Five years of whole-soil warming led to loss of subsoil carbon stocks and increased CO
doi: 10.1126/sciadv.abd1343 pubmed: 34020943 pmcid: 8139586
Frey, S. D. et al. Chronic nitrogen additions suppress decomposition and sequester soil carbon in temperate forests. Biogeochemistry 121, 305–316 (2014).
doi: 10.1007/s10533-014-0004-0
Pregitzer, K. S., Burton, A. J., Zak, D. R. & Talhelm, A. F. Simulated chronic nitrogen deposition increases carbon storage in Northern Temperate forests. Glob. Chang. Biol. 14, 142–153 (2008).
doi: 10.1111/j.1365-2486.2007.01465.x
Liu, L. & Greaver, T. L. A global perspective on belowground carbon dynamics under nitrogen enrichment. Ecol. Lett. 13, 819–828 (2010).
doi: 10.1111/j.1461-0248.2010.01482.x pubmed: 20482580
Zak, D. R., Pregitzer, K. S., Burton, A. J., Edwards, I. P. & Kellner, H. Microbial responses to a changing environment: implications for the future functioning of terrestrial ecosystems. Fungal Ecol. 4, 386–395 (2011).
doi: 10.1016/j.funeco.2011.04.001
Lovett, G. M. et al. Nitrogen addition increases carbon storage in soils, but not in trees, in an Eastern U.S. deciduous forest. Ecosystems 16, 980–1001 (2013).
doi: 10.1007/s10021-013-9662-3
Wang, J. J. et al. Long-term nitrogen addition suppresses microbial degradation, enhances soil carbon storage, and alters the molecular composition of soil organic matter. Biogeochemistry 142, 299–313 (2019).
doi: 10.1007/s10533-018-00535-4
Bradford, M. A. et al. Cross-biome patterns in soil microbial respiration predictable from evolutionary theory on thermal adaptation. Nat. Ecol. Evol. 3, 223–231 (2019).
doi: 10.1038/s41559-018-0771-4 pubmed: 30643243
Wang, M. et al. Global soil profiles indicate depth-dependent soil carbon losses under a warmer climate. Nat. Commun. 13, 5514 (2022).
doi: 10.1038/s41467-022-33278-w pubmed: 36127349 pmcid: 9489695
Pisani, O., Frey, S. D., Simpson, A. J. & Simpson, M. J. Soil warming and nitrogen deposition alter soil organic matter composition at the molecular-level. Biogeochemistry 123, 391–409 (2015).
doi: 10.1007/s10533-015-0073-8
Zak, D. R. et al. Anthropogenic N deposition increases soil organic matter accumulation without altering its biochemical composition. Glob. Chang. Biol. 23, 933–944 (2017).
doi: 10.1111/gcb.13480 pubmed: 27562874
Wang, J. J. et al. Long-term nitrogen addition alters the composition of soil-derived dissolved organic matter. ACS Earth Space Chem. 4, 189–201 (2020).
doi: 10.1021/acsearthspacechem.9b00262
vandenEnden, L., Anthony, M. A., Frey, S. D. & Simpson, M. J. Biogeochemical evolution of soil organic matter composition after a decade of warming and nitrogen addition. Biogeochemistry 156, 161–175 (2021).
doi: 10.1007/s10533-021-00837-0
Stoica, I. et al. Chronic warming and nitrogen-addition alters soil organic matter molecular composition distinctly in tandem compared to individual stressors. ACS Earth Space Chem. 7, 609–622 (2023).
doi: 10.1021/acsearthspacechem.2c00380
Frey, S. D., Knorr, M., Parrent, J. L. & Simpson, R. T. Chronic nitrogen enrichment affects the structure and function of the soil microbial community in temperate hardwood and pine forests. For. Ecol. Manage. 196, 159–171 (2004).
doi: 10.1016/j.foreco.2004.03.018
Anthony, M. A., Knorr, M., Moore, J. A. M., Simpson, M. & Frey, S. D. Fungal community and functional responses to soil warming are greater than for soil nitrogen enrichment. Elem. Sci. Anth. 9, 000059 (2021).
doi: 10.1525/elementa.2021.000059
Garcia, M. O. et al. Soil microbes trade-off biogeochemical cycling for stress tolerance traits in response to year-round climate change. Front. Microbiol. 11, 616 (2020).
doi: 10.3389/fmicb.2020.00616 pubmed: 32477275 pmcid: 7238748
Jansson, J. K. & Hofmockel, K. S. Soil microbiomes and climate change. Nat. Rev. Microbiol. 18, 35–46 (2020).
doi: 10.1038/s41579-019-0265-7 pubmed: 31586158
Morrison, E. W. et al. Warming alters fungal communities and litter chemistry with implications for soil carbon stocks. Soil Biol. Biochem. 132, 120–130 (2019).
doi: 10.1016/j.soilbio.2019.02.005
Cheng, L. et al. Warming enhances old organic carbon decomposition through altering functional microbial communities. ISME J. 11, 1825–1835 (2017).
doi: 10.1038/ismej.2017.48 pubmed: 28430189 pmcid: 5520036
Moore, J. A. M. et al. Fungal community structure and function shifts with atmospheric nitrogen deposition. Glob. Chang. Biol. 27, 1349–1364 (2020).
doi: 10.1111/gcb.15444 pubmed: 33159820
Lilleskov, E. A., Kuyper, T. W., Bidartondo, M. I. & Hobbie, E. A. Atmospheric nitrogen deposition impacts on the structure and function of forest mycorrhizal communities: a review. Environ. Pollut. 246, 148–162 (2019).
doi: 10.1016/j.envpol.2018.11.074 pubmed: 30543941
Zhang, T., Chen, H. Y. H. & Ruan, H. Global negative effects of nitrogen deposition on soil microbes. ISME J. 12, 1817–1825 (2018).
doi: 10.1038/s41396-018-0096-y pubmed: 29588494 pmcid: 6018792
Morrison, E. W. et al. Chronic nitrogen additions fundamentally restructure the soil fungal community in a temperate forest. Fungal Ecol. 23, 48–57 (2016).
doi: 10.1016/j.funeco.2016.05.011
Tunison, R., Wood, T., Reed, S. & Cavaleri, M. Respiratory acclimation of tropical forest roots in response to in situ experimental warming and hurricane disturbance. Ecosystems 27, 168–184 (2024).
doi: 10.1007/s10021-023-00880-y
Burton, A., Pregitzer, K., Ruess, R., Hendrick, R. & Allen, M. Root respiration in North American forests: effects of nitrogen concentration and temperature across biomes. Oecologia 131, 559–568 (2002).
doi: 10.1007/s00442-002-0931-7 pubmed: 28547551
Burton, A. J., Melillo, J. M. & Frey, S. D. Adjustment of forest ecosystem root respiration as temperature warms. J. Integr. Plant Biol. 50, 1467–1483 (2008).
doi: 10.1111/j.1744-7909.2008.00750.x pubmed: 19017133
Han, M. & Zhu, B. Linking root respiration to chemistry and morphology across species. Glob. Chang. Biol. 27, 190–201 (2021).
doi: 10.1111/gcb.15391 pubmed: 33058350
Pregitzer, K. S., Laskowski, M. J., Burton, A. J., Lessard, V. C. & Zak, D. R. Variation in sugar maple root respiration with root diameter and soil depth. Tree Physiol. 18, 665–670 (1998).
doi: 10.1093/treephys/18.10.665 pubmed: 12651416
McCormack, L., Adams, T. S., Smithwick, E. A. H. & Eissenstat, D. M. Predicting fine root lifespan from plant functional traits in temperate trees. New Phytol. 195, 823–831 (2012).
doi: 10.1111/j.1469-8137.2012.04198.x
Bai, T., Wang, P., Qiu, Y., Zhang, Y. & Hu, S. Nitrogen availability mediates soil carbon cycling response to climate warming: a meta-analysis. Glob. Chang. Biol. 29, 2608–2626 (2023).
doi: 10.1111/gcb.16627 pubmed: 36744998
Canarini, A., Kaiser, C., Merchant, A., Richter, A. & Wanek, W. Root exudation of primary metabolites: mechanisms and their roles in plant responses to environmental stimuli. Front. Plant Sci. 10, 157 (2019).
doi: 10.3389/fpls.2019.00157 pubmed: 30881364 pmcid: 6407669
Sun, L., Ataka, M., Kominami, Y. & Yoshimura, K. Relationship between fine-root exudation and respiration of two Quercus species in a Japanese temperate forest. Tree Physiol. 37, 1011–1020 (2017).
doi: 10.1093/treephys/tpx026 pubmed: 28338964
Clemmensen, K. E. et al. Carbon sequestration is related to mycorrhizal fungal community shifts during long-term succession in boreal forests. New Phytol. 205, 1525–1536 (2015).
doi: 10.1111/nph.13208 pubmed: 25494880
Gale, W. J. & Cambardella, C. A. Carbon dynamics of surface residue- and root-derived organic matter under simulated no-till. Soil Sci. Soc. Am. J 64, 190–195 (2000).
doi: 10.2136/sssaj2000.641190x
Godbold, D. L. et al. Mycorrhizal hyphal turnover as a dominant process for carbon input into soil organic matter. Plant Soil 281, 15–24 (2006).
doi: 10.1007/s11104-005-3701-6
Frey, S. D. Mycorrhizal fungi as mediators of soil organic matter dynamics. Annu. Rev. Ecol. Evol. Syst. 50, 237–259 (2019).
doi: 10.1146/annurev-ecolsys-110617-062331
Contosta, A. R., Frey, S. D. & Cooper, A. B. Seasonal dynamics of soil respiration and N mineralization in chronically warmed and fertilized soils. Ecosphere 2, 1–21 (2011).
doi: 10.1890/ES10-00133.1
Boose, E. Fisher Meteorological Station at Harvard Forest since 2001. Harvard Forest Data Archive: HF001v.26 (2021); https://harvardforest1.fas.harvard.edu/exist/apps/datasets/showData.html?id=HF001
Contosta, A. R., Frey, S. D., Ollinger, S. V. & Cooper, A. B. Soil respiration does not acclimatize to warmer temperatures when modeled over seasonal timescales. Biogeochemistry 112, 555–570 (2013).
doi: 10.1007/s10533-012-9748-6
Rumpel, C. et al. Alteration of soil organic matter following treatment with hydrofluoric acid (HF). Org. Geochem. 37, 1437–1451 (2006).
doi: 10.1016/j.orggeochem.2006.07.001
Conte, P., Spaccini, R. & Piccolo, A. State of the art of CPMAS
doi: 10.1016/j.pnmrs.2004.02.002
Preston, C. M. Environmental NMR: solid-state methods. eMagRes 3, 29–42 (2014).
Sun, S. et al. Soil warming and nitrogen deposition alter soil respiration, microbial community structure and organic carbon composition in a coniferous forest on eastern Tibetan Plateau. Geoderma 353, 283–292 (2019).
doi: 10.1016/j.geoderma.2019.07.023
Baldock, J. A., Oades, J. M. & Waters, A. G. Aspects of the chemical structure of soil organic materials as revealed by solid-state
doi: 10.1007/BF02402261
Ostertag, R., Marín-Spiotta, E., Silver, W. L. & Schulten, J. Litterfall and decomposition in relation to soil carbon pools along a secondary forest chronosequence in Puerto Rico. Ecosystems 11, 701–714 (2008).
doi: 10.1007/s10021-008-9152-1
Spohn, M., Klaus, K., Wanek, W. & Richter, A. Microbial carbon use efficiency and biomass turnover times depending on soil depth – implications for carbon cycling. Soil Biol. Biochem. 96, 74–81 (2016).
doi: 10.1016/j.soilbio.2016.01.016
Spohn, M. et al. Soil microbial carbon use efficiency and biomass turnover in a long-term fertilization experiment in a temperate grassland. Soil Biol. Biochem. 97, 168–175 (2016).
doi: 10.1016/j.soilbio.2016.03.008
Persson, H. A. & Stadenberg, I. Spatial distribution of fine-roots in boreal forests in eastern Sweden. Plant Soil 318, 1–14 (2009).
doi: 10.1007/s11104-008-9811-1
Jarvi, M. P. & Burton, A. J. Root respiration and biomass responses to experimental soil warming vary with root diameter and soil depth. Plant Soil 451, 435–446 (2020).
doi: 10.1007/s11104-020-04540-1
Paradiso, E., Jevon, F. & Matthes, J. Fine root respiration is more strongly correlated with root traits than tree species identity. Ecosphere 10, e02944 (2019).
doi: 10.1002/ecs2.2944
Melillo, J. M. et al. Soil warming, carbon–nitrogen interactions, and forest carbon budgets. Proc. Natl Acad. Sci. USA 108, 9508–9512 (2011).
doi: 10.1073/pnas.1018189108 pubmed: 21606374 pmcid: 3111267
Bradford, M. A. et al. Thermal adaptation of soil microbial respiration to elevated temperature. Ecol. Lett. 11, 1316–1327 (2008).
doi: 10.1111/j.1461-0248.2008.01251.x pubmed: 19046360
Richardson, A. D. et al. Comparing simple respiration models for eddy flux and dynamic chamber data. Agric. For. Meteorol. 141, 219–234 (2006).
doi: 10.1016/j.agrformet.2006.10.010
Groemping, U. Relative importance for linear regression in R: the package relaimpo. J. Stat. Softw. 17, 1–27 (2006).
R v.3.5.1 (R Foundation for Statistical Computing, 2021).
R v.3.1-153 (R Foundation for Statistical Computing, 2021).

Auteurs

Melissa A Knorr (MA)

Center for Soil Biogeochemistry and Microbial Ecology, University of New Hampshire, Durham, NH, USA. mel.knorr@unh.edu.
Department of Natural Resources and the Environment, University of New Hampshire, Durham, NH, USA. mel.knorr@unh.edu.

A R Contosta (AR)

Department of Natural Resources and the Environment, University of New Hampshire, Durham, NH, USA.
Earth Systems Research Center, Institute for the Study of Earth, Oceans, and Space, University of New Hampshire, Durham, NH, USA.

E W Morrison (EW)

Department of Natural Resources and the Environment, University of New Hampshire, Durham, NH, USA.

T J Muratore (TJ)

Center for Soil Biogeochemistry and Microbial Ecology, University of New Hampshire, Durham, NH, USA.
Department of Natural Resources and the Environment, University of New Hampshire, Durham, NH, USA.

M A Anthony (MA)

Center for Microbiology and Environmental Systems Science, University of Vienna, Vienna, Austria.

I Stoica (I)

Department of Physical and Environmental Sciences and Environmental NMR Centre, University of Toronto Scarborough, Toronto, Ontario, Canada.

K M Geyer (KM)

Department of Environmental Science and Sustainability, Allegheny College, Meadville, PA, USA.

M J Simpson (MJ)

Department of Physical and Environmental Sciences and Environmental NMR Centre, University of Toronto Scarborough, Toronto, Ontario, Canada.

S D Frey (SD)

Center for Soil Biogeochemistry and Microbial Ecology, University of New Hampshire, Durham, NH, USA. serita.frey@unh.edu.
Department of Natural Resources and the Environment, University of New Hampshire, Durham, NH, USA. serita.frey@unh.edu.

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