Relative contribution of biogenic and anthropogenic sources to formic and acetic acids in the atmospheric boundary layer

被引:33
作者
Glasius, M
Boel, C
Bruun, N
Easa, LM
Hornung, P
Klausen, HS
Klitgaard, KC
Lindeskov, C
Moller, CK
Nissen, H
Petersen, APF
Kleefeld, S
Boaretto, E
Hansen, TS
Heinemeier, J
Lohse, C
机构
[1] Odense Univ, Dept Chem, DK-5230 Odense M, Denmark
[2] Aarhus Univ, Dept Phys & Astron, Accelerator Mass Spectrometry 14C Dating Lab, DK-8000 Aarhus, Denmark
来源
JOURNAL OF GEOPHYSICAL RESEARCH-ATMOSPHERES | 2001年 / 106卷 / D7期
关键词
D O I
10.1029/2000JD900676
中图分类号
P4 [大气科学(气象学)];
学科分类号
0706 ; 070601 ;
摘要
Formic and acetic acids are ubiquitous trace gases in ambient air, but their sources remain to be fully understood, They originate fi om photochemical oxidation of volatile organic compounds (VOC). Direct emissions of these carboxylic acids are supposedly negligible at North European conditions. Radiocarbon analysis of formic and acetic acids provides information oil tale origin of the precursor VOC, since biogenic VOC have the same C-14/C-12 ratio as atmospheric carbon dioxide, while VOC emitted from fossil fuels are devoid of C-14. The origin of atmospheric formic and acetic acids was studied by accelerator mass spectrometry of air and rainwater samples. Sampling sites were selected at different distances from centers of anthropogenic activities in Europe, ranging from urban via rural to remote sites. Tie procedure for preparation of samples was checked by several quality assurance samples, and no significant contamination from atmospheric carbon dioxide was observed. The results show very high (55-100%) biogenic contributions to both carboxylic acids in ail samples. Only in semiurban and urban areas were the biogenic fractions less than 80%. The results indicate that biogenic VOC can have substantial influence on formation of photochemical oxidation products and thus photochemical oxidants.
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收藏
页码:7415 / 7426
页数:12
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