قالب وردپرس درنا توس
Home / Science / Loss of carbon in the soil from experimental warming in a tropical forest

Loss of carbon in the soil from experimental warming in a tropical forest



  • 1.

    Jackson, RB et al. Soil carbon ecology: pools, vulnerabilities, and biotic and abiotic controls. Annu. Rev. Ekol. Evol. syst. 48, 41

    9–445 (2017).

    Google Scholar

  • 2.

    CIAIA, P. et al. in Climate Change 2013: Basics of Physical Sciences. Contribution of Working Group I to the Fifth Assessment Report of the Intergovernmental Panel on Climate Change (eds Stocker, TF et al.) Ch. 6 (Cambridge Univ. Press, 2013).

  • 3.

    Melillo, JM et al. Long-term model and magnitude of ground carbon response to climate system in a heating world. science 358, 101-105 (2017).

    ADS CAS PubMed Google Scholar

  • 4.

    van Gestel, N. et al. Prediction of carbon loss in the soil with heating. nature 554, E4 – E5 (2018).

    PubMed Google Scholar

  • 5.

    Davidson, EA & Janssens, IA Sensitivity to carbon decomposition temperature in the soil and reactions to climate change. nature 440, 165–173 (2006).

    ADS Scholar Google Scholar

  • 6.

    Hicks Pries, CE, Castanha, C., Porras, RC & Torn, MS Carbon flux throughout the earth in response to heat. science 355, 1420–1423 (2017).

    ADS CAS PubMed Google Scholar

  • 7.

    Carey, JC et al. Soil respiration temperature reaction largely unchanged with experimental heating. Proc. Natl Acad. Sci. US 113, 13797–13802 (2016).

    ADS Scholar Google Scholar

  • 8.

    Wood, TE et al. in Consequences of global warming ecosystem: Microbes, vegetation, fauna and soil biogeochemistry (ed. Mohan, JE) Ch. 14, 385–439 (Academic Press, 2019).

  • 9.

    Pan, Y. et al. A large and continuous carbon sink in the forests of the world. science 333, 988–993 (2011).

    ADS CAS PubMed Google Scholar

  • 10.

    Anderson-Teixeira, KJ, Wang, MMH, McGarvey, JC & LeBauer, DS Carbon dynamics of mature and regrowth tropical forests derived from a pantropic database (TropForC-db). Glob. Change Biol. 22, 1690–1709 (2016).

    ADS Google Scholar

  • 11.

    Malhi, Y. Productivity, metabolism and carbon cycle of tropical forest vegetation. J. Ecol. 100, 65–75 (2012).

    CAS Scholar Google

  • 12.

    Chambers, JQ et al. Breathing from a tropical forest ecosystem: resource segregation and low carbon utilization efficiency. Ecol. appl. 14, 72–88 (2004).

    Google Scholar

  • 13.

    Romero-Olivares, AL, Allison, SD & Treseder, KK Soil microbes and their response to experimental warming over time: a meta-analysis of field studies. Soil biol. Biochem. 107, 32–40 (2017).

    CAS Scholar Google

  • 14.

    Tang, J. et al. in Consequences of global warming ecosystem: Microbes, vegetation, fauna and soil biogeochemistry (ed. Mohan, JE) Ch. 8, 175–201 (Academic Press, 2019).

  • 15.

    Nottingham, AT et al. Climate warming and soil carbon in tropical forests: mirrors from an uplift gradient in the Peruvian Andes. Bioscience 65, 906–921 (2015).

    PubMed Scholar PubMed Central Google

  • 16.

    Todd-Brown, KEO et al. Causes of change in ground carbon predictions by CMIP5 Earth system models and comparison with observations. Biogeosciences 10, 1717–1736 (2013).

    ADS Google Scholar

  • 17.

    Intergovernmental Panel on Climate Change (IPCC). Global warming of 1.5 ° C: A special IPCC report on the impacts of global warming of 1.5 ° C above pre-industrial levels and paths associated with global greenhouse gases, in the context of strengthening the global response to the threat of climate change, Sustainable Development and Poverty Eradication Efforts (eds Masson-Delmotte, V. et at.) Ch. 3 (World Meteorological Organization, 2018).

  • 18.

    Cox, PM et al. The sensitivity of tropical carbon to climate change is limited by the variability of carbon dioxide. nature 494, 341–344 (2013).

    ADS CAS PubMed Google Scholar

  • 19.

    Mora, C. et al. Estimated time of departure from climate from recent variability. nature 502, 183–187 (2013).

    ADS CAS PubMed Google Scholar

  • 20.

    Beaumont, LJ et al. Impacts of climate change on the most extraordinary ecoregions in the world. Proc. Natl Acad. Sci. US 108, 2306–2311 (2011).

    ADS CAS PubMed Google Scholar

  • 21.

    Steidinger, BS et al. Climate decomposition controls guide the global biogeography of forest tree symbiosis. nature 569, 404–408 (2019).

    ADS CAS PubMed Google Scholar

  • 22.

    Rubio, VE & Detto, M. Spatial variability of soil respiration in a seasonal tropical forest. Ecol. evol. 7, 7104–7116 (2017).

    Google PubMed PubMed Central Scholar

  • 23.

    Frey, SD, Lee, J., Melillo, JM & Six, J. Temperature response of soil microbial efficiency and its responses to climate. Nat. Clim. chang. 3, 395–398 (2013).

    ADS Scholar Google Scholar

  • 24.

    Bradford, MA Thermal adaptation of decomposer communities in soil warming. Front. Microbiol. 4, https://doi.org/10.3389/fmicb.2013.00333 (2013).

  • 25.

    Wang, XH et al. A doubling of the carbon cycle sensitivity to tropical temperature changes. nature 506, 212–215 (2014).

    ADS CAS PubMed Google Scholar

  • 26.

    Liu, JJ et al. Answers to the carbon cycle responses of tropical continents in El Nino 2015-2016. science 358, eaam5690 (2017).

    PubMed Google Scholar

  • 27.

    Karhu, K. et al. Sensitivity to soil respiration rate temperature increased by the reaction of the microbial community. nature 513, 81–84 (2014).

    ADS CAS PubMed Google Scholar

  • 28.

    Bradford, MA et al. Cross-biome models in soil microbial respiration predictable by evolutionary theory on thermal adaptation. Nat. Ecol. Evol. 3, 223–231 (2019).

    Google Scholar

  • 29.

    Wieder, RK & Wright, SJ Tropical forest waste dynamics and dry season irrigation in Barro Colorado Island, Panama. ecology 76, 1971–1979 (1995).

    Google Scholar

  • 30.

    Chave, J. et al. Spatial and temporal variation of biomass in a tropical forest: results from a large census plot in Panama. J. Ecol. 91, 240–252 (2003).

    Google Scholar

  • 31.

    Nottingham, AT et al. Microbial responses to heat increase soil carbon loss after shifting to a tropical forest uplift gradient. Ecol. Lett. 22, 1889–1899 (2019).

    PubMed Google Scholar

  • 32.

    Crowther, TW et al. The amount of global carbon losses on earth in response to heat. nature 540, 104-108 (2016).

    ADS CAS PubMed Google Scholar

  • 33.

    Leigh, EGJ Tropical Forest Ecology: A View of Barro Island Colorado (Oxford Univ. Press, 1999).

    Google Scholar

  • 34.

    Woodring, WP Geology of Barro Colorado Island. Smithson. Misc. gather. 135, 1–39 (1958).

    Google Scholar

  • 35.

    Sanchez, PA & Logan, TJ Myths and science about soil chemistry and fertility in the tropics. Spec SSSA. publ. 29, 35–46 (1992).

    CAS Scholar Google

  • 36.

    Hanson, PJ et al. A method for experimental heating of intact soil profiles for application in climate change experiments. Glob. Change Biol. 17, 1083-1096 (2011).

    ADS Google Scholar

  • 37.

    Nottingham, AT, Turner, BL, Winter, K., van der Heijden, MGA & Tanner, EVJ Mycorrhizal mycobacterial Arbuscular mycelial respiration in a humid tropical forest. Phytol i ri. 186, 957–967 (2010).

    CAS PubMed Google Scholar

  • 38.

    Cavelier, J. Thin root biomass and soil properties in a semicircular forest and a lower montani rain forest in Panama. Plant soil 142, 187–201 (1992).

    CAS Scholar Google

  • 39.

    Sinsabaugh, RL et al. Stoichiometry of the efficiency of microbial carbon use in soils. Ecol. Monogr. 86, 172–189 (2016).

    Google Scholar

  • 40.

    Hendershot, WH & Duquette, M. A simple barium-chloride method for determining cation and exchangeable cation exchange capacity. Sci Earth. Soc. Am. J. 50, 605–608 (1986).

    ADS Google Scholar

  • 41.

    Brooks, PC, Landman, A., Pruden, G. & Jenkinson, DS chloroform fumigation and soil nitrogen release – a rapid direct extraction method to measure microbial biomass nitrogen in the soil. Soil biol. Biochem. 17, 837–842 (1985).

    CAS Scholar Google

  • 42.

    Vance, ED, Brooks, PC & Jenkinson, DS An extraction method for measuring soil microbial biomass-C. Soil biol. Biochem. 19, 703–707 (1987).

    CAS Scholar Google

  • 43.

    Jenkinson, DS, Brooks, PC & Powlson, DS Measurement of soil microbial biomass. Soil biol. Biochem. 36, 5-7 (2004).

    CAS Scholar Google

  • 44.

    Kouno, K., Tuchiya, Y. & Ando, ​​T. Measurement of soil microbial biomass phosphorus by an anion exchange method. Soil biol. Biochem. 27, 1353–1357 (1995).

    CAS Scholar Google

  • 45.

    Nottingham, AT et al. Soil microbial nutrient constraints along a tropical forest uplift gradient: an underground test of a biogochemical paradigm. Biogeosciences 12, 6489–6523 (2015).

    Google Scholar

  • 46.

    Nottingham, AT et al. Sensitivity to the temperature of soil enzymes along an uplift gradient in the Peruvian Andes. biogeochemistry 127, 217–230 (2016).

    Google Scholar

  • 47.

    Turner, BL & Romero, TE Short-term changes in inorganic nutrients extracted during conservation of rainforest soils. Sci Earth. Soc. Am. J. 73, 1972-1979 (2009).

  • 48.

    Zuur, AF, Ieno, EN, Walker, NJ, Saveliev, AA & Smith, GM Models and Mixed Effects in Ecology with R (Springer, 2007).


  • Source link