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DOI10.5194/acp-18-15017-2018
Adjoint inversion of Chinese non-methane volatile organic compound emissions using space-based observations of formaldehyde and glyoxal
Cao, Hansen1,2; Fu, Tzung-May1,2; Zhang, Lin1,2; Henze, Daven K.3; Miller, Christopher Chan4; Lerot, Christophe5; Abad, Gonzalo Gonzalez4; De Smedt, Isabelle5; Zhang, Qiang6; van Roozendael, Michel5; Hendrick, Francois5; Chance, Kelly4; Li, Jie7; Zheng, Junyu8; Zhao, Yuanhong1,2
2018-10-19
发表期刊ATMOSPHERIC CHEMISTRY AND PHYSICS
ISSN1680-7316
EISSN1680-7324
出版年2018
卷号18期号:20页码:15017-15046
文章类型Article
语种英语
国家Peoples R China; USA; Belgium
英文摘要

We used the GEOS-Chem model and its adjoint to quantify Chinese non-methane volatile organic compound (NMVOC) emissions for the year 2007, using the tropospheric column concentrations of formaldehyde and glyoxal observed by the Global Ozone Monitoring Experiment 2A (GOME-2A) instrument and the Ozone Monitoring Instrument (OMI) as quantitative constraints. We conducted a series of inversion experiments using different combinations of satellite observations to explore their impacts on the topdown emission estimates. Our top-down estimates for Chinese annual total NMVOC emissions were 30.7 to 49.5 (average 41.9) Tg yr(-1), including 16.4 to 23.6 (average 20.2) Tg yr(-1) from anthropogenic sources, 12.2 to 22.8 (average 19.2) Tg yr(-1) from biogenic sources, and 2.08 to 3.13 (average 2.48) Tg yr(-1) from biomass burning. In comparison, the a priori estimate for Chinese annual total NMVOC emissions was 38.3 Tg yr(-1), including 18.8 Tg yr(-1) from anthropogenic sources, 17.3 Tg yr(-1) from biogenic sources, and 2.27 Tg yr(-1) from biomass burning. The simultaneous use of glyoxal and formaldehyde observations helped distinguish the NMVOC species from different sources and was essential in constraining anthropogenic emissions. Our four in- version experiments consistently showed that the Chinese anthropogenic emissions of NMVOC precursors of glyoxal were larger than the a priori estimates. Our top-down estimates for Chinese annual emission of anthropogenic aromatics (benzene, toluene, and xylene) ranged from 5.5 to 7.9 Tg yr(-1), 2 % to 46 % larger than the estimate of the a priori emission inventory (5.4 Tg yr(-1)). Three out of our four inversion experiments indicated that the seasonal variation in Chinese NMVOC emissions was significantly stronger than indicated in the a priori inventory. Model simulations driven by the average of our top-down NMVOC emission estimates (which had a stronger seasonal variation than the a priori) showed that surface afternoon ozone concentrations over eastern China increased by 1-8 ppb in June and decreased by 1-10 ppb in December relative to the simulations using the a priori emissions and were in better agreement with measurements. We concluded that the satellite observations of formaldehyde and glyoxal together provided quantitative constraints on the emissions and source types of NMVOCs over China and improved our understanding on regional chemistry.


领域地球科学
收录类别SCI-E
WOS记录号WOS:000447779800002
WOS关键词OZONE MONITORING INSTRUMENT ; MASTER CHEMICAL MECHANISM ; GLOBAL FIRE EMISSIONS ; MAX-DOAS OBSERVATIONS ; MCM V3 PART ; ISOPRENE EMISSIONS ; AROMATIC-HYDROCARBONS ; TROPOSPHERIC DEGRADATION ; ANTHROPOGENIC EMISSIONS ; GAS-PHASE
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/30892
专题地球科学
作者单位1.Peking Univ, Sch Phys, Dept Atmospher & Ocean Sci, Beijing 100871, Peoples R China;
2.Peking Univ, Sch Phys, Lab Climate & Ocean Atmosphere Studies, Beijing 100871, Peoples R China;
3.Univ Colorado, Dept Mech Engn, Boulder, CO 80309 USA;
4.Harvard Smithsonian Ctr Astrophys, Atom & Mol Phys Div, 60 Garden St, Cambridge, MA 02138 USA;
5.Belgian Inst Space Aeron, Brussels, Belgium;
6.Tsinghua Univ, Ctr Earth Syst Sci, Beijing, Peoples R China;
7.Chinese Acad Sci, Inst Atmospher Phys, Beijing, Peoples R China;
8.South China Univ Technol, Coll Environm Sci & Engn, Guangzhou, Guangdong, Peoples R China
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GB/T 7714
Cao, Hansen,Fu, Tzung-May,Zhang, Lin,et al. Adjoint inversion of Chinese non-methane volatile organic compound emissions using space-based observations of formaldehyde and glyoxal[J]. ATMOSPHERIC CHEMISTRY AND PHYSICS,2018,18(20):15017-15046.
APA Cao, Hansen.,Fu, Tzung-May.,Zhang, Lin.,Henze, Daven K..,Miller, Christopher Chan.,...&Zhao, Yuanhong.(2018).Adjoint inversion of Chinese non-methane volatile organic compound emissions using space-based observations of formaldehyde and glyoxal.ATMOSPHERIC CHEMISTRY AND PHYSICS,18(20),15017-15046.
MLA Cao, Hansen,et al."Adjoint inversion of Chinese non-methane volatile organic compound emissions using space-based observations of formaldehyde and glyoxal".ATMOSPHERIC CHEMISTRY AND PHYSICS 18.20(2018):15017-15046.
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