HUSCAP logo Hokkaido Univ. logo

Hokkaido University Collection of Scholarly and Academic Papers >
Institute of Low Temperature Science >
Peer-reviewed Journal Articles, etc >

Size-distributions of n-alkanes, PAHs and hopanes and their sources in the urban, mountain and marine atmospheres over East Asia

This item is licensed under: Creative Commons Attribution 3.0 Unported

Files in This Item:
ACP9-22_8869-8882.pdf4.98 MBPDFView/Open
Please use this identifier to cite or link to this item:http://hdl.handle.net/2115/44511

Title: Size-distributions of n-alkanes, PAHs and hopanes and their sources in the urban, mountain and marine atmospheres over East Asia
Authors: Wang, G. Browse this author
Kawamura, K. Browse this author →KAKEN DB
Xie, M. Browse this author
Hu, S. Browse this author
Gao, S. Browse this author
Cao, J. Browse this author
An, Z. Browse this author
Wang, Z. Browse this author
Issue Date: 23-Nov-2009
Publisher: Copernicus Publications
Journal Title: Atmospheric Chemistry and Physics
Volume: 9
Issue: 22
Start Page: 8869
End Page: 8882
Publisher DOI: 10.5194/acp-9-8869-2009
Abstract: Size-segregated (9 stages) n-alkanes, polycyclic aromatic hydrocarbons (PAHs) and hopanes in the urban (Baoji city in inland China), mountain (Mt. Tai in east coastal China) and marine (Okinawa Island, Japan) atmospheres over East Asia were studied using a GC/MS technique. Ambient concentrations of n-alkanes (1698±568 ng m^[-3] in winter and 487±145 ng m^[-3] in spring), PAHs (536±80 and 161±39 ng m^[-3]), and hopanes (65±24 and 20±2.4 ng m^[-3]) in the urban air are 1-2 orders of magnitude higher than those in the mountain aerosols and 2-3 orders of magnitude higher than those in the marine samples. Mass ratios of n-alkanes, PAHs and hopanes clearly demonstrate coal-burning emissions as their major source. Size distributions of fossil fuel derived n-alkane, PAHs and hopanes were found to be unimodal in most cases, peaking at 0.7-1.1 μm size. In contrast, plant wax derived n-alkanes presented a bimodal distribution with two peaks at the sizes of 0.7-1.1 μm and >4.7 μm in the summer mountain and spring marine samples. Among the three types of samples, geometric mean diameter (GMD) of the organics in fine mode (<2.1 μm) was found to be smallest (av. 0.63 μm in spring) for the urban samples and largest (1.01 μm) for the marine samples, whereas the GMD in coarse mode (≥2.1 μm) was found to be smallest (3.48 μm) for the marine aerosols and largest (4.04 μm) for the urban aerosols. The fine mode GMDs of the urban and mountain samples were larger in winter than in spring and summer. Moreover, GMDs of 3- and 4-ring PAHs were larger than those of 5- and 6-ring PAHs in the three types of atmospheres. Such differences in GMDs can be interpreted by the repartitioning of organic compounds and the coagulation and hygroscopic growth of particles during a long-range transport from the inland continent to the marine area, as well as the difference in their sources among the three regions.
Rights: http://creativecommons.org/licenses/by/3.0/
Type: article
URI: http://hdl.handle.net/2115/44511
Appears in Collections:低温科学研究所 (Institute of Low Temperature Science) > 雑誌発表論文等 (Peer-reviewed Journal Articles, etc)

Submitter: 河村 公隆

Export metadata:

OAI-PMH ( junii2 , jpcoar )

MathJax is now OFF:


 

 - Hokkaido University