Factors Controlling DMS Emission and Atmospheric Sulfate Aerosols in the Western Pacific Continental Sea

Author:

Yan Shi‐Bo123ORCID,Xu Gao‐Bin3,Zhang Hong‐Hai13ORCID,Wang Jian3,Xu Feng13,Gao Xu‐Xu14,Zhang Jia‐Wei5,Wu Jin‐Wei13,Yang Gui‐Peng123ORCID

Affiliation:

1. Key Laboratory of Marine Chemistry Theory and Technology Frontiers Science Center for Deep Ocean Multispheres and Earth System Ministry of Education Qingdao China

2. Laboratory of Marine Ecology and Environmental Science Laoshan Laboratory Qingdao China

3. College of Chemistry and Chemical Engineering/Center for Ocean Carbon Neutrality Ocean University of China Qingdao China

4. Institute of Marine Science and Technology Shandong University Qingdao China

5. Eco‐Environmental Monitoring and Research Center Pearl River Valley and South China Sea Ecology and Environment Administration Ministry of Ecology and Environment Guangzhou China

Abstract

AbstractThe western Pacific continental sea significantly influences the regulation of climate‐active gases budget and the burden of sulfate aerosols. An underway shipboard measurement device was used to determine the dimethyl sulfide (DMS) in the surface seawater and overlying atmosphere in the East China Continental Sea. The average concentration of DMS in atmosphere and seawater was 122.8 ± 86.2pptv and 6.47 ± 3.58 nmol L−1, respectively. The variation trend of surface water DMS in the western Pacific continental sea was influenced by the abundance and composition of phytoplankton under different ocean current systems, with a significant impact from eddies on DMS production in the South China Sea. By eliminating the influence of terrestrial sources and limiting air mass transport within the marine boundary layer, strong correlations were established between atmospheric DMS and air mass exposure to chlorophyll (Echl), as well as between aerosol methanesulfonic acid (MSA) and Echl. During the aerosol sampling period, the atmospheric DMS levels (1,057 ± 371 ng/m3) were significantly higher than MSA levels (46.3 ± 59.8 ng/m3) in the East China Sea, where the conversion of DMS to MSA was not affected by changes in DMS concentration. The sea‐to‐air fluxes of DMS varied over a wide range, from 0.02 to 156.0 μmol m−2 d−1, with an average of 14.35 ± 18.58 μmol m−2 d−1. Marine DMS emissions play a critical role in the formation of sulfur aerosols on the western Pacific continental shelf, accounting for 24.6 ± 7.6% (14.8%–37.8%) of the total sulfate aerosols.

Funder

National Natural Science Foundation of China

Fundamental Research Funds for the Central Universities

Publisher

American Geophysical Union (AGU)

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