Atmospheric aerosol compositions over the South China Sea: temporal variability and source apportionment

In order to evaluate impacts of different source emission on marine atmospheric particles over the South China Sea (SCS), major inorganic ionic concentrations (Na<sup>+</sup>, Cl<sup>−</sup>, SO<sub>4</sub><sup>2−</sup>, Ca<sup>2+</sup>, Mg...

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Main Authors: H.-W. Xiao, H.-Y. Xiao, L. Luo, C.-Y. Shen, A.-M. Long, L. Chen, Z.-H. Long, D.-N. Li
Format: Article
Language:English
Published: Copernicus Publications 2017-03-01
Series:Atmospheric Chemistry and Physics
Online Access:http://www.atmos-chem-phys.net/17/3199/2017/acp-17-3199-2017.pdf
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spelling doaj-60f03685633e4bb9a768ad5e2ac6ef762020-11-24T22:32:24ZengCopernicus PublicationsAtmospheric Chemistry and Physics1680-73161680-73242017-03-011743199321410.5194/acp-17-3199-2017Atmospheric aerosol compositions over the South China Sea: temporal variability and source apportionmentH.-W. Xiao0H.-Y. Xiao1L. Luo2C.-Y. Shen3A.-M. Long4L. Chen5Z.-H. Long6D.-N. Li7Laboratory of Atmospheric Environment, Key Laboratory of Nuclear Resources and Environment (Ministry of Education), East China University of Technology, Nanchang 330013, ChinaLaboratory of Atmospheric Environment, Key Laboratory of Nuclear Resources and Environment (Ministry of Education), East China University of Technology, Nanchang 330013, ChinaLaboratory of Atmospheric Environment, Key Laboratory of Nuclear Resources and Environment (Ministry of Education), East China University of Technology, Nanchang 330013, ChinaCollege of Fisheries, Guangdong Ocean University, Zhanjiang 524088, ChinaState Key Laboratory of Tropical Oceanography, South China Sea Institute of Oceanology, Chinese Academy of Sciences, Guangzhou 510301, China Xisha Deep Sea Marine Environment Observation and Research Station, South China Sea Institute of Oceanology, Chinese Academy of Sciences, Sansha 573199, ChinaXisha Deep Sea Marine Environment Observation and Research Station, South China Sea Institute of Oceanology, Chinese Academy of Sciences, Sansha 573199, ChinaXisha Deep Sea Marine Environment Observation and Research Station, South China Sea Institute of Oceanology, Chinese Academy of Sciences, Sansha 573199, ChinaIn order to evaluate impacts of different source emission on marine atmospheric particles over the South China Sea (SCS), major inorganic ionic concentrations (Na<sup>+</sup>, Cl<sup>−</sup>, SO<sub>4</sub><sup>2−</sup>, Ca<sup>2+</sup>, Mg<sup>2+</sup>, K<sup>+</sup>, NH<sub>4</sub><sup>+</sup> and NO<sub>3</sub><sup>−</sup>) were determined in total suspended particulates (TSPs) at Yongxing Island, from March 2014 to February 2015. The annual average concentration of TSPs was 89.6 ± 68.0 µg m<sup>−3</sup>, with 114.7 ± 82.1, 60.4 ± 27.0 and 59.5 ± 25.6 µg m<sup>−3</sup> in cool, warm and transition seasons, respectively. Cl<sup>−</sup> had the highest concentration, with an annual average of 7.73 ± 5.99 µg m<sup>−3</sup>, followed by SO<sub>4</sub><sup>2−</sup> (5.54 ± 3.65 µg m<sup>−3</sup>), Na<sup>+</sup> (4.00 ± 1.88 µg m<sup>−3</sup>), Ca<sup>2+</sup> (2.15 ± 1.54 µg m<sup>−3</sup>), NO<sub>3</sub><sup>−</sup> (1.95 ± 1.34 µg m<sup>−3</sup>), Mg<sup>2+</sup> (0.44 ± 0.33 µg m<sup>−3</sup>), K<sup>+</sup> (0.33 ± 0.22 µg m<sup>−3</sup>) and NH<sub>4</sub><sup>+</sup> (0.07 ± 0.07 µg m<sup>−3</sup>). Concentrations of TSPs and the major ions showed seasonal variations, which were higher in the cool season and lower in the warm and transition seasons. Factors of influence were wind speed, temperature, relatively humidity, rain and air mass source region. Back trajectories, concentration-weighted trajectories (CWTs), and positive matrix factorization (PMF) of chemical compositions were analyzed for source apportionment, source contribution and spatiotemporal variation of major ions. Back trajectories and CWTs showed that air masses at Yongxing Island were mainly from the northeast, southwest and southeast in the cool, warm and transition seasons, respectively. The PMF results showed that 77.4 % of Na<sup>+</sup> and 99.3 % of Cl<sup>−</sup> were from sea salt; 60.5 % of NH<sub>4</sub><sup>+</sup> was from oceanic emission. Anthropogenic sources were very important for atmospheric aerosols over the island. Secondary inorganic aerosol of SO<sub>2</sub> and NO<sub><i>x</i></sub> from fossil fuel combustion (especially coal in Chinese coastal regions) was the dominant source of NO<sub>3</sub><sup>−</sup> (69.5 %) and SO<sub>4</sub><sup>2−</sup> (57.5 %).http://www.atmos-chem-phys.net/17/3199/2017/acp-17-3199-2017.pdf
collection DOAJ
language English
format Article
sources DOAJ
author H.-W. Xiao
H.-Y. Xiao
L. Luo
C.-Y. Shen
A.-M. Long
L. Chen
Z.-H. Long
D.-N. Li
spellingShingle H.-W. Xiao
H.-Y. Xiao
L. Luo
C.-Y. Shen
A.-M. Long
L. Chen
Z.-H. Long
D.-N. Li
Atmospheric aerosol compositions over the South China Sea: temporal variability and source apportionment
Atmospheric Chemistry and Physics
author_facet H.-W. Xiao
H.-Y. Xiao
L. Luo
C.-Y. Shen
A.-M. Long
L. Chen
Z.-H. Long
D.-N. Li
author_sort H.-W. Xiao
title Atmospheric aerosol compositions over the South China Sea: temporal variability and source apportionment
title_short Atmospheric aerosol compositions over the South China Sea: temporal variability and source apportionment
title_full Atmospheric aerosol compositions over the South China Sea: temporal variability and source apportionment
title_fullStr Atmospheric aerosol compositions over the South China Sea: temporal variability and source apportionment
title_full_unstemmed Atmospheric aerosol compositions over the South China Sea: temporal variability and source apportionment
title_sort atmospheric aerosol compositions over the south china sea: temporal variability and source apportionment
publisher Copernicus Publications
series Atmospheric Chemistry and Physics
issn 1680-7316
1680-7324
publishDate 2017-03-01
description In order to evaluate impacts of different source emission on marine atmospheric particles over the South China Sea (SCS), major inorganic ionic concentrations (Na<sup>+</sup>, Cl<sup>−</sup>, SO<sub>4</sub><sup>2−</sup>, Ca<sup>2+</sup>, Mg<sup>2+</sup>, K<sup>+</sup>, NH<sub>4</sub><sup>+</sup> and NO<sub>3</sub><sup>−</sup>) were determined in total suspended particulates (TSPs) at Yongxing Island, from March 2014 to February 2015. The annual average concentration of TSPs was 89.6 ± 68.0 µg m<sup>−3</sup>, with 114.7 ± 82.1, 60.4 ± 27.0 and 59.5 ± 25.6 µg m<sup>−3</sup> in cool, warm and transition seasons, respectively. Cl<sup>−</sup> had the highest concentration, with an annual average of 7.73 ± 5.99 µg m<sup>−3</sup>, followed by SO<sub>4</sub><sup>2−</sup> (5.54 ± 3.65 µg m<sup>−3</sup>), Na<sup>+</sup> (4.00 ± 1.88 µg m<sup>−3</sup>), Ca<sup>2+</sup> (2.15 ± 1.54 µg m<sup>−3</sup>), NO<sub>3</sub><sup>−</sup> (1.95 ± 1.34 µg m<sup>−3</sup>), Mg<sup>2+</sup> (0.44 ± 0.33 µg m<sup>−3</sup>), K<sup>+</sup> (0.33 ± 0.22 µg m<sup>−3</sup>) and NH<sub>4</sub><sup>+</sup> (0.07 ± 0.07 µg m<sup>−3</sup>). Concentrations of TSPs and the major ions showed seasonal variations, which were higher in the cool season and lower in the warm and transition seasons. Factors of influence were wind speed, temperature, relatively humidity, rain and air mass source region. Back trajectories, concentration-weighted trajectories (CWTs), and positive matrix factorization (PMF) of chemical compositions were analyzed for source apportionment, source contribution and spatiotemporal variation of major ions. Back trajectories and CWTs showed that air masses at Yongxing Island were mainly from the northeast, southwest and southeast in the cool, warm and transition seasons, respectively. The PMF results showed that 77.4 % of Na<sup>+</sup> and 99.3 % of Cl<sup>−</sup> were from sea salt; 60.5 % of NH<sub>4</sub><sup>+</sup> was from oceanic emission. Anthropogenic sources were very important for atmospheric aerosols over the island. Secondary inorganic aerosol of SO<sub>2</sub> and NO<sub><i>x</i></sub> from fossil fuel combustion (especially coal in Chinese coastal regions) was the dominant source of NO<sub>3</sub><sup>−</sup> (69.5 %) and SO<sub>4</sub><sup>2−</sup> (57.5 %).
url http://www.atmos-chem-phys.net/17/3199/2017/acp-17-3199-2017.pdf
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