Levine, J.G.; Wolff, E.W.; Jones, A.E.
ORCID: https://orcid.org/0000-0002-2040-4841; Sime, L.C.
ORCID: https://orcid.org/0000-0002-9093-7926; Valdes, P.J.; Archibald, A.T.; Carver, G.D.; Warwick, N.J.; Pyle, J.A..
2011
Reconciling the changes in atmospheric-methane sources and sinks between the Last Glacial Maximum and the pre-industrial era.
Geophysical Research Letters, 38 (23), L23804.
6, pp.
10.1029/2011GL049545
Abstract
We know from the ice record that the concentration of
atmospheric methane, [CH4], at the Last Glacial Maximum
(LGM) was roughly half that in the pre-industrial era (PI), buthow 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), implyingthe change in [CH4] was almost entirely source driven―a conclusion that, though subject to significant uncertainties,can be reconciled with recent methane source estimates.
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