Processing of atmospheric organic matter by California radiation fogs

被引:121
作者
Collett, Jeffrey L., Jr. [1 ]
Herckes, Pierre [2 ]
Youngster, Sarah [1 ]
Lee, Taehyoung [1 ]
机构
[1] Colorado State Univ, Dept Atmospher Sci, Ft Collins, CO 80523 USA
[2] Arizona State Univ, Dept Chem & Biochem, Tempe, AZ USA
基金
美国国家科学基金会;
关键词
fog; source marker; organic carbon; air pollution; aerosol;
D O I
10.1016/j.atmosres.2007.11.005
中图分类号
P4 [大气科学(气象学)];
学科分类号
0706 ; 070601 ;
摘要
Considerable effort has been put into characterizing the ionic composition of fogs and clouds over the past twenty-five years. Recently it has become evident that clouds and fogs often contain large concentrations of organic material as well. Here we report findings from a series of studies examining the organic composition of radiation fogs in central California. Organic compounds in these fogs comprise a major fraction of total solute mass, with total organic carbon sometimes reaching levels of several tens of mg/L. This organic matter is comprised of a wide variety of compounds, ranging from low molecular weight organic acids to high molecular weight compounds with molecular masses approaching several hundred to a thousand g/mole. The most abundant individual compounds are typically formic acid, acetic acid, and formaldehyde. High concentrations are also observed of some dicarboxylic acids (e.g., oxalate) and dicarbonyls (e.g., glyoxal and methylglyoxal) and of levoglucosan, an anhydrosugar characteristically emitted by biomass combustion. Many other compounds have been identified in fog water by GUMS, including long chain n-alkanoic acids, n-alkanes, PAH, and others, although these compounds typically comprise a total of only a few percent of fog TOC. Measurements of fog scavenging of organic and elemental carbon reveal preferential scavenging of organic carbon. Tracking of individual organic compounds utilized as source type markers suggests the fogs differentially scavenge carbonaceous particles from different source types, with more active processing of wood smoke than vehicle exhaust. Observations of high deposition velocities of fog-borne organic carbon, in excess of 1 cm/s, indicate that fogs in the region represent an important mechanism for cleansing the atmosphere of pollution. (c) 2007 Elsevier B.V. All rights reserved.
引用
收藏
页码:232 / 241
页数:10
相关论文
共 42 条
[1]   AQUEOUS-PHASE PHOTOCHEMICAL FORMATION OF HYDROGEN-PEROXIDE IN AUTHENTIC CLOUD WATERS [J].
ANASTASIO, C ;
FAUST, BC ;
ALLEN, JM .
JOURNAL OF GEOPHYSICAL RESEARCH-ATMOSPHERES, 1994, 99 (D4) :8231-8248
[2]   Elemental carbon-based method for monitoring occupational exposures to particulate diesel exhaust [J].
Birch, ME ;
Cary, RA .
AEROSOL SCIENCE AND TECHNOLOGY, 1996, 25 (03) :221-241
[3]   Secondary organic aerosol formation in cloud and fog droplets: a literature evaluation of plausibility [J].
Blando, JD ;
Turpin, BJ .
ATMOSPHERIC ENVIRONMENT, 2000, 34 (10) :1623-1632
[4]   Characterization of organic aerosol in Big Bend National Park, Texas [J].
Brown, SG ;
Herckes, P ;
Ashbaugh, L ;
Hannigan, MP ;
Kreidenweis, SM ;
Collett, JL .
ATMOSPHERIC ENVIRONMENT, 2002, 36 (38) :5807-5818
[5]  
Collett JeffreyL., 2001, WATER AIR SOIL POLL, V1, P303, DOI [DOI 10.1023/A:1013175709931, 10.1023/A:101317570]
[6]  
Collett JL, 1999, ATMOS ENVIRON, V33, P129, DOI 10.1016/S1352-2310(98)00136-8
[7]   Cloud condensation nucleus activity of organic compounds: a laboratory study [J].
Corrigan, CE ;
Novakov, T .
ATMOSPHERIC ENVIRONMENT, 1999, 33 (17) :2661-2668
[8]   A study of the ability of pure secondary organic aerosol to act as cloud condensation nuclei [J].
Cruz, CN ;
Pandis, SN .
ATMOSPHERIC ENVIRONMENT, 1997, 31 (15) :2205-2214
[9]   Characterization of water-soluble organic compounds in atmospheric aerosol: A new approach [J].
Decesari, S ;
Facchini, MC ;
Fuzzi, S ;
Tagliavini, E .
JOURNAL OF GEOPHYSICAL RESEARCH-ATMOSPHERES, 2000, 105 (D1) :1481-1489
[10]   On the Caltech Active Strand Cloudwater Collectors [J].
Demoz, BB ;
Collett, JL ;
Daube, BC .
ATMOSPHERIC RESEARCH, 1996, 41 (01) :47-62