Chemical composition and size-fractionated origins of aerosols over a remote coastal site in southern Taiwan

© Taiwan Association for Aerosol Research. In spring 2013 air samples were collected from a coastal site in the sparsely populated far south-west of Taiwan and analysed for ambient gases, inorganic salts, carboxylates, and saccharides. Concentration of ambient gases was in the order SO2> HCl>...

Full description

Saved in:
Bibliographic Details
Main Authors: Ying I. Tsai, Khajornsak Sopajaree, Su Ching Kuo, Ting Yi Hsin
Format: Journal
Published: 2018
Subjects:
Online Access:https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84948747086&origin=inward
http://cmuir.cmu.ac.th/jspui/handle/6653943832/54545
Tags: Add Tag
No Tags, Be the first to tag this record!
Institution: Chiang Mai University
id th-cmuir.6653943832-54545
record_format dspace
spelling th-cmuir.6653943832-545452018-09-04T10:16:00Z Chemical composition and size-fractionated origins of aerosols over a remote coastal site in southern Taiwan Ying I. Tsai Khajornsak Sopajaree Su Ching Kuo Ting Yi Hsin Environmental Science © Taiwan Association for Aerosol Research. In spring 2013 air samples were collected from a coastal site in the sparsely populated far south-west of Taiwan and analysed for ambient gases, inorganic salts, carboxylates, and saccharides. Concentration of ambient gases was in the order SO2> HCl> HNO3> NH3> HNO2. Day-night variation in concentrations indicated that photochemical conversion of HNO2to HNO3occurs during the day. PM2.5(16.16 ± 5.30 μg m–3) accounted for 61.1% of PM10 mass concentrations. The main inorganic salts were SO42–, NH4+, Na+, NO3-, and Cl-, collectively accounting for 48.8 ± 27.4% of the PM2.5. Cldepletion during the day was higher than during the night due to the presence of reactive photochemical products. The average Cl-depletion of PM2.5(53.1%) was markedly higher than that of PM2.5-10(26.0%), indicating that in PM2.5, a high amount of Cl-reacts with acidic gases to form HCl, which then escapes into the atmosphere. The carboxylate concentration in PM2.5was 0.50 ± 0.24 μg m-3. It was found that low-molecular-weight carboxylates formed more readily in the open coastal region than in urban regions of southern Taiwan. Additionally, the daily mean ratio of Oxalate/non-seasalt SO42-(6.15 ± 2.28%) in the coastal region was higher than that in the urban regions in southern Taiwan. The most prevalent saccharide in PM2.5was myo-inosital (333 ± 300 μg m-3), a type of soil fungus metabolite. Emissions of arabitol and mannitol, emitted through lichen and fungal activity, were markedly higher during the day. Only a trace amount (8.92 ± 16.92 μg m-3) of Levoglucosan (Levo), an indicator of biomass burning, was detected. The mean Levo/organic carbon ratio was 5.04 ± 8.72‰, suggesting that biomass burning contributed slightly to aerosols in the study area. An analysis of air mass backward trajectories showed that the products of biomass burning in Southeast Asia and southern China may be transported to the study area through long-range transport. This effect is more noticeable during the day when onshore breezes support the transport of particles sourced from the west of Taiwan. 2018-09-04T10:16:00Z 2018-09-04T10:16:00Z 2015-12-01 Journal 20711409 16808584 2-s2.0-84948747086 10.4209/aaqr.2015.09.0566 https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84948747086&origin=inward http://cmuir.cmu.ac.th/jspui/handle/6653943832/54545
institution Chiang Mai University
building Chiang Mai University Library
country Thailand
collection CMU Intellectual Repository
topic Environmental Science
spellingShingle Environmental Science
Ying I. Tsai
Khajornsak Sopajaree
Su Ching Kuo
Ting Yi Hsin
Chemical composition and size-fractionated origins of aerosols over a remote coastal site in southern Taiwan
description © Taiwan Association for Aerosol Research. In spring 2013 air samples were collected from a coastal site in the sparsely populated far south-west of Taiwan and analysed for ambient gases, inorganic salts, carboxylates, and saccharides. Concentration of ambient gases was in the order SO2> HCl> HNO3> NH3> HNO2. Day-night variation in concentrations indicated that photochemical conversion of HNO2to HNO3occurs during the day. PM2.5(16.16 ± 5.30 μg m–3) accounted for 61.1% of PM10 mass concentrations. The main inorganic salts were SO42–, NH4+, Na+, NO3-, and Cl-, collectively accounting for 48.8 ± 27.4% of the PM2.5. Cldepletion during the day was higher than during the night due to the presence of reactive photochemical products. The average Cl-depletion of PM2.5(53.1%) was markedly higher than that of PM2.5-10(26.0%), indicating that in PM2.5, a high amount of Cl-reacts with acidic gases to form HCl, which then escapes into the atmosphere. The carboxylate concentration in PM2.5was 0.50 ± 0.24 μg m-3. It was found that low-molecular-weight carboxylates formed more readily in the open coastal region than in urban regions of southern Taiwan. Additionally, the daily mean ratio of Oxalate/non-seasalt SO42-(6.15 ± 2.28%) in the coastal region was higher than that in the urban regions in southern Taiwan. The most prevalent saccharide in PM2.5was myo-inosital (333 ± 300 μg m-3), a type of soil fungus metabolite. Emissions of arabitol and mannitol, emitted through lichen and fungal activity, were markedly higher during the day. Only a trace amount (8.92 ± 16.92 μg m-3) of Levoglucosan (Levo), an indicator of biomass burning, was detected. The mean Levo/organic carbon ratio was 5.04 ± 8.72‰, suggesting that biomass burning contributed slightly to aerosols in the study area. An analysis of air mass backward trajectories showed that the products of biomass burning in Southeast Asia and southern China may be transported to the study area through long-range transport. This effect is more noticeable during the day when onshore breezes support the transport of particles sourced from the west of Taiwan.
format Journal
author Ying I. Tsai
Khajornsak Sopajaree
Su Ching Kuo
Ting Yi Hsin
author_facet Ying I. Tsai
Khajornsak Sopajaree
Su Ching Kuo
Ting Yi Hsin
author_sort Ying I. Tsai
title Chemical composition and size-fractionated origins of aerosols over a remote coastal site in southern Taiwan
title_short Chemical composition and size-fractionated origins of aerosols over a remote coastal site in southern Taiwan
title_full Chemical composition and size-fractionated origins of aerosols over a remote coastal site in southern Taiwan
title_fullStr Chemical composition and size-fractionated origins of aerosols over a remote coastal site in southern Taiwan
title_full_unstemmed Chemical composition and size-fractionated origins of aerosols over a remote coastal site in southern Taiwan
title_sort chemical composition and size-fractionated origins of aerosols over a remote coastal site in southern taiwan
publishDate 2018
url https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84948747086&origin=inward
http://cmuir.cmu.ac.th/jspui/handle/6653943832/54545
_version_ 1681424340239777792