Seasonal variation and origins of dicarboxylic acids in the marine atmosphere over the western North Pacific

被引:124
|
作者
Mochida, M
Kawabata, A
Kawamura, K
Hatsushika, H
Yamazaki, K
机构
[1] Hokkaido Univ, Inst Low Temp Sci, Kita Ku, Sapporo, Hokkaido 0600819, Japan
[2] Hokkaido Univ, Grad Sch Environm Earth Sci, Kita Ku, Sapporo, Hokkaido 0600810, Japan
关键词
marine aerosols; Pacific Ocean; East Asia; dicarboxylic acids;
D O I
10.1029/2002JD002355
中图分类号
P4 [大气科学(气象学)];
学科分类号
0706 ; 070601 ;
摘要
[1] Concentrations of homologous (C-2-C-11) dicarboxylic acids were measured in the atmosphere over Chichi-jima Island (27degrees04'N, 142degrees13'E), western North Pacific, from April 1990 to November 1993. The monthly averaged concentrations of straight-chain C-2-C-7 dicarboxylic acids, and some branched, keto-, and unsaturated dicarboxylic acids showed a maximum in winter to spring and a minimum in the summer season. In contrast, straight-chain C-8-C-11 dicarboxylic acids showed an opposite trend with a maximum in spring to summer. Principal component analysis revealed that there is a source characterized by a strong contribution of C-2-C-7 dicarboxylic acids, phthalic acid, some keto- dicarboxylic acids, and unsaturated-dicarboxylic acids, whereas there seems to be another source(s) for the C-8-C-11 dicarboxylic acids. A combined model of backward trajectories and emission inventories was used to better understand the sources and source regions of the dicarboxylic acids. The results show that concentrations of various C-2-C-7 dicarboxylic acids in the western North Pacific atmosphere are largely controlled by their emissions and/or their precursor emissions from anthropogenic sources in the Asian continent, followed by long-range atmospheric transport. On the other hand, longer-chain dicarboxylic acids cannot be explained by long-range atmospheric transport from a continental region, which implies emissions and/or formation from natural sources, possibly from the ocean.
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页数:11
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