4.7 Article

Carbonaceous and inorganic composition in long-range transported aerosols over northern Japan: Implication for aging of water-soluble organic fraction

期刊

ATMOSPHERIC ENVIRONMENT
卷 43, 期 16, 页码 2532-2540

出版社

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.atmosenv.2009.02.032

关键词

Atmospheric aerosols; Major ions; Diacids; Sugars; Water-soluble organic carbon; Organic carbon; Photochemical aging

资金

  1. Japanese Ministry of Education, Science, Sport and Culture [17340166, 19204055]
  2. Japanese Society for the Promotion of Science (JSPS)

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To better understand the influence of sources and atmospheric processing on aerosol chemical composition, we collected atmospheric particles in Sapporo, northern Japan during spring and early summer 2005 under the air mass transport conditions from Siberia, China and surrounding seas. The aerosols were analyzed for inorganic ions, organic carbon (OC), elemental carbon (EC), water-soluble organic carbon (WSOC), and the major water-soluble organic compound classes (i.e., dicarboxylic acids and sugars). SO42- is the most abundant inorganic constituent (average 44% of the identified inorganic ion mass) followed by NH4+ (21%) and NO3- (13%). Concentrations of OC, EC, and WSOC ranged from 2.0-16, 0.24-2.9, and 0.80-7.9 mu g m(-3) with a mean of 7.4, 1.0, and 3.1 mu g m(-3), respectively. High OC/EC ratios (range: 3.6-19, mean: 8.7) were obtained, however WSOC/OC ratios (0.23-0.69, 0.44) do not show any significant diurnal changes. These results suggest that the Sapporo aerosols were already aged. but were not seriously affected by local photochemical processes. Identified water-soluble organic compounds (diacids + sugars) account for <10% of WSOC. Based on some marker species and air mass back trajectory analyses, and using stable carbon isotopic compositions of shorter-chain diacids (i.e., C-2-C-4) as photochemical aging factor of organic aerosols, the present study suggests that a fraction of WSOC in OC is most likely influenced by aerosol aging, although the OC loading in aerosols may be more influenced by their sources and source regions. (C) 2009 Elsevier Ltd. All rights reserved.

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