Abrupt changes in biomass burning during the last glacial period

• 成果类型: Article
• 署名作者: Riddell-Young, Ben; Lee, James Edward; Brook, Edward J.; Schmitt, Jochen; Fischer, Hubertus; Bauska, Thomas K.; Menking, James A.; Iseli, Rene; Clark, Justin Reid
• 署名单位: Oregon State University; University of Colorado System; University of Colorado Boulder; United States Department of Energy (DOE); Los Alamos National Laboratory; University of Bern; University of Bern; UK Research & Innovation (UKRI); Natural Environment Research Council (NERC); NERC British Antarctic Survey; Commonwealth Scientific & Industrial Research Organisation (CSIRO); University of Fribourg; University of Colorado System; University of Colorado Boulder
• 刊物名称: Nature
• ISSN/ISSBN: 0028-2952
• DOI: 10.1038/s41586-024-08363-3
• 发表日期: 2025-01-02
• 关键词: deep ice core; atmospheric methane; carbon-cycle; isotopic composition; wd2014 chronology; source signatures; asian monsoon; rapid changes; fire regimes; trace gases

摘要

Understanding the causes of past atmospheric methane (CH4) variability is important for characterizing the relationship between CH4, global climate and terrestrial biogeochemical cycling. Ice core records of atmospheric CH4 contain rapid variations linked to abrupt climate changes of the last glacial period known as Dansgaard-Oeschger (DO) events and Heinrich events (HE)1,2. The drivers of these CH4 variations remain unknown but can be constrained with ice core measurements of the stable isotopic composition of atmospheric CH4, which is sensitive to the strength of different isotopically distinguishable emission categories (microbial, pyrogenic and geologic)3, 4-5. Here we present multi-decadal-scale measurements of delta 13C-CH4 and delta D-CH4 from the WAIS Divide and Talos Dome ice cores and identify abrupt 1 parts per thousand enrichments in delta 13C-CH4 synchronous with HE CH4 pulses and 0.5 parts per thousand delta 13C-CH4 enrichments synchronous with DO CH4 increases. delta D-CH4 varied little across the abrupt CH4 changes. Using box models to interpret these isotopic shifts6 and assuming a constant delta 13C-CH4 of microbial emissions, we propose that abrupt shifts in tropical rainfall associated with HEs and DO events enhanced 13C-enriched pyrogenic CH4 emissions, and by extension global wildfire extent, by 90-150%. Carbon cycle box modelling experiments7 suggest that the resulting released terrestrial carbon could have caused from one-third to all of the abrupt CO2 increases associated with HEs. These findings suggest that fire regimes and the terrestrial carbon cycle varied contemporaneously and substantially with past abrupt climate changes of the last glacial period.