期刊
GEOPHYSICAL RESEARCH LETTERS
卷 38, 期 -, 页码 -出版社
AMER GEOPHYSICAL UNION
DOI: 10.1029/2011GL049545
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资金
- Natural Environment Research Council
- French Institut National des Sciences de l'Univers
- National Centre for Atmospheric Science
- NERC [NE/E007600/1, bas0100024] Funding Source: UKRI
- Natural Environment Research Council [NE/E007600/1, bas0100024, ncas10009] Funding Source: researchfish
We know from the ice record that the concentration of atmospheric methane, [CH(4)], at the Last Glacial Maximum (LGM) was roughly half that in the pre-industrial era (PI), but how much of the difference was source-driven, and how much was sink-driven, remains uncertain. Recent developments include: a higher estimate of the LGM-PI change in methane emissions from wetlands-the dominant, natural methane source; and the possible recycling of OH consumed in isoprene oxidation-the principal methane sink. Here, in view of these developments, we use an atmospheric chemistry-transport model to re-examine the main factors affecting OH during this period: changes in air temperature and emissions of non-methane volatile organic compounds from vegetation. We find that their net effect was negligible (with and without an OH recycling mechanism), implying the change in [CH(4)] was almost entirely source driven-a conclusion that, though subject to significant uncertainties, can be reconciled with recent methane source estimates. Citation: Levine, J. G., E. W. Wolff, A. E. Jones, L. C. Sime, P. J. Valdes, A. T. Archibald, G. D. Carver, N. J. Warwick, and J. A. Pyle (2011), Reconciling the changes in atmospheric methane sources and sinks between the Last Glacial Maximum and the pre-industrial era, Geophys. Res. Lett., 38, L23804, doi: 10.1029/2011GL049545.
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