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Improved Constraints on Global Methane Emissions and Sinks Using δ13C-CH4We study the drivers behind the global atmospheric methane (CH4) increase observed after 2006. Candidate emission and sink scenarios are constructed based on proposed hypotheses in the literature. These scenarios are simulated in the TM5 tracer transport model for 1984–2016 to produce three-dimensional fields of CH4 and δ13C-CH4, which are compared with observations to test the competing hypotheses in the literature in one common model framework. We find that the fossil fuel (FF) CH4 emission trend from the Emissions Database for Global Atmospheric Research 4.3.2 inventory does not agree with observed δ13C-CH4. Increased FF CH4 emissions are unlikely to be the dominant driver for the post-2006 global CH4 increase despite the possibility for a small FF emission increase. We also find that a significant decrease in the abundance of hydroxyl radicals (OH) cannot explain the post-2006 global CH4 increase since it does not track the observed decrease in global mean δ13C-CH4. Different CH4 sinks have different fractionation factors for δ13C-CH4, thus we can investigate the uncertainty introduced by the reaction of CH4 with tropospheric chlorine (Cl), a CH4 sink whose abundance, spatial distribution, and temporal changes remain uncertain. Our results show that including or excluding tropospheric Cl as a 13 Tg/year CH4 sink in our model changes the magnitude of estimated fossil emissions by ∼20%. We also found that by using different wetland emissions based on a static versus a dynamic wetland area map, the partitioning between FF and microbial sources differs by 20 Tg/year, ∼12% of estimated fossil emissions.
Document ID
20210015886
Acquisition Source
Goddard Space Flight Center
Document Type
Accepted Manuscript (Version with final changes)
Authors
X. Lan ORCID
(University of Colorado Boulder Boulder, Colorado, United States)
S. Basu ORCID
(Universities Space Research Association Columbia, Maryland, United States)
S. Schwietzke ORCID
(University of Colorado Boulder Boulder, Colorado, United States)
L. M. P. Bruhwiler ORCID
(National Oceanic and Atmospheric Administration Washington D.C., District of Columbia, United States)
E. J. Dlugokencky ORCID
(National Oceanic and Atmospheric Administration Washington D.C., District of Columbia, United States)
S. E. Michel ORCID
(University of Colorado Boulder Boulder, Colorado, United States)
O. A. Sherwood ORCID
(University of Colorado Boulder Boulder, Colorado, United States)
P. P. Tans ORCID
(National Oceanic and Atmospheric Administration Washington D.C., District of Columbia, United States)
K. Thoning ORCID
(National Oceanic and Atmospheric Administration Washington D.C., District of Columbia, United States)
G. Etiope ORCID
(National Institute of Geophysics and Volcanology Rome, Italy)
Q. Zhuang ORCID
(Purdue University West Lafayette West Lafayette, Indiana, United States)
L. Liu
(Purdue University West Lafayette West Lafayette, Indiana, United States)
Y. Oh ORCID
(National Oceanic and Atmospheric Administration Washington D.C., District of Columbia, United States)
J. B. Miller ORCID
(National Oceanic and Atmospheric Administration Washington D.C., District of Columbia, United States)
G. Pétron ORCID
(Cooperative Institute for Research in Environmental Sciences Boulder, Colorado, United States)
B. H. Vaughn ORCID
(Institute of Arctic and Alpine Research Boulder, Colorado, United States)
M. Crippa
(Joint Research Centre Ispra, Italy)
Date Acquired
May 20, 2021
Publication Date
May 8, 2021
Publication Information
Publication: Global Biogeochemical Cycles
Publisher: American Geophysical Union / Wiley
Volume: 35
Issue: 6
Issue Publication Date: June 1, 2021
ISSN: 0886-6236
e-ISSN: 1944-9224
Subject Category
Earth Resources And Remote Sensing
Environment Pollution
Funding Number(s)
CONTRACT_GRANT: NNX17AE79A
CONTRACT_GRANT: NNX17AK20G
Distribution Limits
Public
Copyright
Use by or on behalf of the US Gov. Permitted.
Technical Review
External Peer Committee
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