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Variability and Quasi-Decadal Changes in the Methane Budget over the Period 2000-2012

Authors :
Saunois, Marielle
Bousquet, Philippe
Poulter, Ben
Peregon, Anna
Ciais, Philippe
Canadell, Josep G
Dlugokencky, Edward J
Etiope, Giuseppe
Bastviken, David
Houweling, Sander
Janssens-Maenhout, Greet
Tubiello, Francesco N
Castaldi, Simona
Jackson, Robert B
Alexe, Mihai
Arora, Vivek K
Beerling, David J
Bergamaschi, Peter
Blake, Donald R
Brailsford, Gordon
Bruhwiler, Lori
Crevoisier, Cyril
Crill, Patrick
Covey, Kristofer
Frankenberg, Christian
Gedney, Nicola
Höglund-Isaksson, Lena
Ishizawa, Misa
Ito, Akihiko
Joos, Fortunat
Kim, Heon-Sook
Kleinen, Thomas
Krummel, Paul
Lamarque, Jean-François
Langenfelds, Ray
Locatelli, Robin
Machida, Toshinobu
Maksyutov, Shamil
Melton, Joe R
Morino, Isamu
Naik, Vaishali
O’Doherty, Simon
Parmentier, Frans-JanW
Patra, Prabir K
Peng, Changhui
Peng, Shushi
Peters, Glen P
Pison, Isabelle
Prinn, Ronald
Ramonet, Michel
Riley, William J
Saito, Makoto
Santini, Monia
Schroeder, Ronny
Simpson, Isobel J
Spahni, Renato
Takizawa, Atsushi
Thornton, Brett F
Tian, Hanqin
Tohjima, Yasunori
Viovy, Nicolas
Voulgarakis, Apostolos
Weiss, Ray
Wilton, David J
Wiltshire, Andy
Worthy, Doug
Wunch, Debra
Xu, Xiyan
Yoshida, Yukio
Zhang, Bowen
Zhang, Zhen
Zhu, and Qiuan
Source :
Atmospheric Chemistry and Physics. 20(18)
Publication Year :
2017
Publisher :
United States: NASA Center for Aerospace Information (CASI), 2017.

Abstract

Following the recent Global Carbon Project (GCP) synthesis of the decadal methane (CH4) budget over 2000- 2012, we analyse here the same dataset with a focus on quasi-decadal and inter-annual variability in CH4 emissions. The GCP dataset integrates results from top-down studies (exploiting atmospheric observations within an atmospheric inverse-modelling framework) and bottom-up models (including process-based models for estimating land surface emissions and atmospheric chemistry), inventories of anthropogenic emissions, and data-driven approaches. The annual global methane emissions from top-down studies, which by construction match the observed methane growth rate within their uncertainties, all show an increase in total methane emissions over the period 2000-2012, but this increase is not linear over the 13 years. Despite differences between individual studies, the mean emission anomaly of the top-down ensemble shows no significant trend in total methane emissions over the period 2000-2006, during the plateau of atmospheric methane mole fractions, and also over the period 2008-2012, during the renewed atmospheric methane increase. However, the top-down ensemble mean produces an emission shift between 2006 and 2008, leading to 22 [16-32] Tg CH4 yr(exp -1) higher methane emissions over the period 2008-2012 compared to 2002-2006. This emission increase mostly originated from the tropics, with a smaller contribution from mid-latitudes and no significant change from boreal regions. The regional contributions remain uncertain in top-down studies. Tropical South America and South and East Asia seem to contribute the most to the emission increase in the tropics. However, these two regions have only limited atmospheric measurements and remain therefore poorly constrained. The sectorial partitioning of this emission increase between the periods 2002-2006 and 2008-2012 differs from one atmospheric inversion study to another. However, all top-down studies suggest smaller changes in fossil fuel emissions (from oil, gas, and coal industries) compared to the mean of the bottom-up inventories included in this study. This difference is partly driven by a smaller emission change in China from the top-down studies compared to the estimate in the Emission Database for Global Atmospheric Research (EDGARv4.2) inventory, which should be revised to smaller values in a near future. We apply isotopic signatures to the emission changes estimated for individual studies based on five emission sectors and find that for six individual top-down studies (out of eight) the average isotopic signature of the emission changes is not consistent with the observed change in atmospheric 13CH4. However, the partitioning in emission change derived from the ensemble mean is consistent with this isotopic constraint. At the global scale, the top-down ensemble mean suggests that the dominant contribution to the resumed atmospheric CH4 growth after 2006 comes from microbial sources (more from agriculture and waste sectors than from natural wetlands), with an uncertain but smaller contribution from fossil CH4 emissions. In addition, a decrease in biomass burning emissions (in agreement with the biomass burning emission databases) makes the balance of sources consistent with atmospheric 13CH4 observations. In most of the top-down studies included here, OH concentrations are considered constant over the years (seasonal variations but without any inter-annual variability). As a result, the methane loss (in particular through OH oxidation) varies mainly through the change in methane concentrations and not its oxidants. For these reasons, changes in the methane loss could not be properly investigated in this study, although it may play a significant role in the recent atmospheric methane changes as briefly discussed at the end of the paper.

Details

Language :
English
ISSN :
16807324 and 16807316
Volume :
20
Issue :
18
Database :
NASA Technical Reports
Journal :
Atmospheric Chemistry and Physics
Notes :
NNX07AK10G, , RCN 209701, , DE-CC GA01101, , DE-CC GA01081, , NNX14AO73G, , NAG5-12669, , NNX11AF16G, , NNX11AF17G, , NNX07AE89G, , NNX11AF15G, , NNX07AF09G, , NNX07AE87G, , SRC VR/ERC 725546, , NNX12AP84G, , DE-AC02-05CH11231, , NE/J00748X/1, , CDREG 322998
Publication Type :
Report
Accession number :
edsnas.20180002887
Document Type :
Report
Full Text :
https://doi.org/10.5194/acp-17-11135-2017