GSTDTAP  > 地球科学
DOI10.5194/acp-17-8371-2017
Detectability of Arctic methane sources at six sites performing continuous atmospheric measurements
Thonat, Thibaud1; Saunois, Marielle1; Bousquet, Philippe1; Pison, Isabelle1; Tan, Zeli2; Zhuang, Qianlai3; Crill, Patrick M.4,5; Thornton, Brett F.4,5; Bastviken, David6; Dlugokencky, Ed J.7; Zimov, Nikita8; Laurila, Tuomas9; Hatakka, Juha10; Hermansen, Ove10; Worthy, Doug E. J.11
2017-07-11
发表期刊ATMOSPHERIC CHEMISTRY AND PHYSICS
ISSN1680-7316
EISSN1680-7324
出版年2017
卷号17期号:13
文章类型Article
语种英语
国家France; USA; Sweden; Russia; Finland; Norway; Canada
英文摘要

Understanding the recent evolution of methane emissions in the Arctic is necessary to interpret the global methane cycle. Emissions are affected by significant uncertainties and are sensitive to climate change, leading to potential feedbacks. A polar version of the CHIMERE chemistry-transport model is used to simulate the evolution of tropospheric methane in the Arctic during 2012, including all known regional anthropogenic and natural sources, in particular freshwater emissions which are often overlooked in methane modelling. CHIMERE simulations are compared to atmospheric continuous observations at six measurement sites in the Arctic region. In winter, the Arctic is dominated by anthropogenic emissions; emissions from continental seepages and oceans, including from the East Siberian Arctic Shelf, can contribute significantly in more limited areas. In summer, emissions from wetland and freshwater sources dominate across the whole region. The model is able to reproduce the seasonality and synoptic variations of methane measured at the different sites. We find that all methane sources significantly affect the measurements at all stations at least at the synoptic scale, except for biomass burning. In particular, freshwater systems play a decisive part in summer, representing on average between 11 and 26% of the simulated Arctic methane signal at the sites. This indicates the relevance of continuous observations to gain a mechanistic understanding of Arctic methane sources. Sensitivity tests reveal that the choice of the land-surface model used to prescribe wetland emissions can be critical in correctly representing methane mixing ratios. The closest agreement with the observations is reached when using the two wetland models which have emissions peaking in August-September, while all others reach their maximum in JuneJuly. Such phasing provides an interesting constraint on wetland models which still have large uncertainties at present. Also testing different freshwater emission inventories leads to large differences in modelled methane. Attempts to include methane sinks (OH oxidation and soil uptake) reduced the model bias relative to observed atmospheric methane. The study illustrates how multiple sources, having different spatiotemporal dynamics and magnitudes, jointly influence the overall Arctic methane budget, and highlights ways towards further improved assessments.


领域地球科学
收录类别SCI-E
WOS记录号WOS:000405372800001
WOS关键词GLOBAL FIRE EMISSIONS ; TERRESTRIAL ECOSYSTEMS ; SATELLITE RETRIEVALS ; NATURAL WETLANDS ; NORTHERN LAKES ; CH4 EMISSIONS ; FOSSIL-FUEL ; IN-SITU ; MODEL ; FLUXES
WOS类目Environmental Sciences ; Meteorology & Atmospheric Sciences
WOS研究方向Environmental Sciences & Ecology ; Meteorology & Atmospheric Sciences
引用统计
文献类型期刊论文
条目标识符http://119.78.100.173/C666/handle/2XK7JSWQ/30716
专题地球科学
作者单位1.Univ Paris Saclay, LSCE, IPSL, CEA CNRS UVSQ, F-91191 Gif Sur Yvette, France;
2.Pacific Northwest Natl Lab, Richland, WA USA;
3.Purdue Univ, Dept Earth Atmospher & Planetary Sci, W Lafayette, IN 47907 USA;
4.Dept Geol Sci, Svante Arrhenius Vag 8, S-10691 Stockholm, Sweden;
5.Bolin Ctr Climate Res, Svante Arrhenius Vag 8, S-10691 Stockholm, Sweden;
6.Linkoping Univ, Dept Themat Studies Environm Change, S-58183 Linkoping, Sweden;
7.NOAA, Earth Syst Res Lab, Global Monitoring Div, Boulder, CO USA;
8.Northeast Sci Stn, Cherskiy, Russia;
9.Finnish Meteorol Inst, Climate & Global Change Res, Helsinki, Finland;
10.NILU Norwegian Inst Air Res, Kjeller, Norway;
11.Environm Canada, Toronto, ON, Canada
推荐引用方式
GB/T 7714
Thonat, Thibaud,Saunois, Marielle,Bousquet, Philippe,et al. Detectability of Arctic methane sources at six sites performing continuous atmospheric measurements[J]. ATMOSPHERIC CHEMISTRY AND PHYSICS,2017,17(13).
APA Thonat, Thibaud.,Saunois, Marielle.,Bousquet, Philippe.,Pison, Isabelle.,Tan, Zeli.,...&Worthy, Doug E. J..(2017).Detectability of Arctic methane sources at six sites performing continuous atmospheric measurements.ATMOSPHERIC CHEMISTRY AND PHYSICS,17(13).
MLA Thonat, Thibaud,et al."Detectability of Arctic methane sources at six sites performing continuous atmospheric measurements".ATMOSPHERIC CHEMISTRY AND PHYSICS 17.13(2017).
条目包含的文件
条目无相关文件。
个性服务
推荐该条目
保存到收藏夹
查看访问统计
导出为Endnote文件
谷歌学术
谷歌学术中相似的文章
[Thonat, Thibaud]的文章
[Saunois, Marielle]的文章
[Bousquet, Philippe]的文章
百度学术
百度学术中相似的文章
[Thonat, Thibaud]的文章
[Saunois, Marielle]的文章
[Bousquet, Philippe]的文章
必应学术
必应学术中相似的文章
[Thonat, Thibaud]的文章
[Saunois, Marielle]的文章
[Bousquet, Philippe]的文章
相关权益政策
暂无数据
收藏/分享
所有评论 (0)
暂无评论
 

除非特别说明,本系统中所有内容都受版权保护,并保留所有权利。