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dc.contributor.authorMing Tung Chuangen_US
dc.contributor.authorChung Te Leeen_US
dc.contributor.authorCharles C.K. Chouen_US
dc.contributor.authorGuenter Englingen_US
dc.contributor.authorShih Yu Changen_US
dc.contributor.authorShuenn Chin Changen_US
dc.contributor.authorGuey Rong Sheuen_US
dc.contributor.authorNeng Huei Linen_US
dc.contributor.authorKhajornsak Sopajareeen_US
dc.contributor.authorYou Jia Changen_US
dc.contributor.authorGuo Jun Hongen_US
dc.date.accessioned2018-09-05T02:59:11Z-
dc.date.available2018-09-05T02:59:11Z-
dc.date.issued2016-07-01en_US
dc.identifier.issn18732844en_US
dc.identifier.issn13522310en_US
dc.identifier.other2-s2.0-84966453580en_US
dc.identifier.other10.1016/j.atmosenv.2016.03.042en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84966453580&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/55642-
dc.description.abstract© 2016 Elsevier Ltd. The transport of biomass burning (BB) aerosol from Indochina may cause a potential effect on climate change in Southeast Asia, East Asia, and the Western Pacific. Up to now, the understanding of BB aerosol composition modification during long-range transport (LRT) is still very limited due to the lack of observational data. In this study, atmospheric aerosols were collected at the Suthep/Doi Ang Khang (DAK) mountain sites in Chiang Mai, Thailand and the Lulin Atmospheric Background Station (Mt. Lulin) in central Taiwan from March to April 2010 and from February to April 2013, respectively. During the study period, an upwind and downwind relationship between the Suthep/DAK and Lulin sites (2400 km apart) was validated by backward trajectories. Comprehensive aerosol properties were resolved for PM2.5water-soluble inorganic ions, carbonaceous content, water-soluble/insoluble organic carbon (WSOC/WIOC), dicarboxylic acids and their salts (DCAS), and anhydrosugars. A Modification Factor (MF) is proposed by employing non-sea-salt potassium ion (nss-K+) or fractionalized elemental carbon evolved at 580 °C after pyrolized OC correction (EC1-OP) as a BB aerosol tracer to evaluate the mass fraction changes of aerosol components from source to receptor regions during LRT. The MF values of nss-SO42-, NH4+, NO3-, OC1 (fractionalized organic carbon evolved from room temperature to 140 °C), OP (pyrolized OC fraction), DCAS, and WSOC were above unity, which indicated that these aerosol components were enhanced during LRT as compared with those in the near-source region. In contrast, the MF values of anhydrosugars ranged from 0.1 to 0.3, indicating anhydrosugars have degraded during LRT.en_US
dc.subjectEarth and Planetary Sciencesen_US
dc.subjectEnvironmental Scienceen_US
dc.titleAerosol transport from Chiang Mai, Thailand to Mt. Lulin, Taiwan - Implication of aerosol aging during long-range transporten_US
dc.typeJournalen_US
article.title.sourcetitleAtmospheric Environmenten_US
article.volume137en_US
article.stream.affiliationsNational Central University Taiwanen_US
article.stream.affiliationsAcademia Sinica Taiwanen_US
article.stream.affiliationsNational Tsing Hua Universityen_US
article.stream.affiliationsDesert Research Institute Reno, Division of Atmospheric Sciencesen_US
article.stream.affiliationsChung Shan Medical Universityen_US
article.stream.affiliationsNational Defense Medical Center Taiwanen_US
article.stream.affiliationsEnvironmental Protection Administration, Taiwanen_US
article.stream.affiliationsChiang Mai Universityen_US
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