Methane dynamics regulated by microbial community response to permafrost thaw

• Published in: Nature
• Main Authors: McCalley, Carmody, Woodcroft, Ben, Hodgkins, Suzanne, Wehr, Richard, Kim, Eun-Hae, Mondav, Rhiannon, Crill, Patrick, Chanton, Jeffrey, Rich, Virginia, Tyson, Gene, Saleska, Scott
• Format: Article in Journal/Newspaper
• Language: English
• Published: Department of Ecology and Evolutionary Biology, University of Arizona 2014
• Subjects: biogeochemistry; climate change; microbial ecology; stable isotopes; methane; Geosciences; Multidisciplinary; Multidisciplinär geovetenskap; permafrost
• Online Access: http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-233744; https://doi.org/10.1038/nature13798

Permafrost contains about 50% of the global soil carbon1. It is thought that the thawing of permafrost can lead to a loss of soil carbon in the form of methane and carbon dioxide emissions2, 3. The magnitude of the resulting positive climate feedback of such greenhouse gas emissions is still unknown3 and may to a large extent depend on the poorly understood role of microbial community composition in regulating the metabolic processes that drive such ecosystem-scale greenhouse gas fluxes. Here we show that changes in vegetation and increasing methane emissions with permafrost thaw are associated with a switch from hydrogenotrophic to partly acetoclastic methanogenesis, resulting in a large shift in the δ13C signature (10–15‰) of emitted methane. We used a natural landscape gradient of permafrost thaw in northern Sweden4, 5 as a model to investigate the role of microbial communities in regulating methane cycling, and to test whether a knowledge of community dynamics could improve predictions of carbon emissions under loss of permafrost. Abundance of the methanogen Candidatus ‘Methanoflorens stordalenmirensis’6 is a key predictor of the shifts in methane isotopes, which in turn predicts the proportions of carbon emitted as methane and as carbon dioxide, an important factor for simulating the climate feedback associated with permafrost thaw in global models3, 7. By showing that the abundance of key microbial lineages can be used to predict atmospherically relevant patterns in methane isotopes and the proportion of carbon metabolized to methane during permafrost thaw, we establish a basis for scaling changing microbial communities to ecosystem isotope dynamics. Our findings indicate that microbial ecology may be important in ecosystem-scale responses to global change. funded by US Department of Energy Office of Biological and Environmental Research (award DE-SC0004632) IsoGenie