Effects of natural and anthropogenic emissions on the composition and toxicity of aerosols in the marine atmosphere

被引:9
|
作者
Song, Sang-Keun [1 ]
Shon, Zang-Ho [2 ]
Bae, Min-Suk [3 ]
Cho, Seong-Bin [1 ]
Moon, Soo-Hwan [1 ]
Kim, Heon-Sook [2 ]
Son, Young Baek [4 ]
Lee, Chang-Rae [5 ]
机构
[1] Jeju Natl Univ, Dept Earth & Marine Sci, Jeju 63243, South Korea
[2] Dong Eui Univ, Dept Environm Engn, Busan 47340, South Korea
[3] Mokpo Natl Univ, Dept Environm Engn, Muan 58554, South Korea
[4] Korea Inst Ocean Sci & Technol KIOST, Jeju Int Marine Sci Ctr Res & Educ, Jeju 63349, South Korea
[5] Natl Pk Res Inst, Marine Res Ctr, Yeosu 59723, South Korea
基金
新加坡国家研究基金会;
关键词
Aerosol toxicity; Dimethyl sulfide (DMS); Methane sulfonic acid (MSA); CMAQ; PM2.5; Ship emission; REDUCED SULFUR-COMPOUNDS; AIRBORNE PARTICULATE MATTER; DIMETHYL SULFIDE; AIR-POLLUTION; PHOTOCHEMICAL OXIDATION; DINEOF RECONSTRUCTION; SULFATE AEROSOL; BIOGENIC SULFUR; SHIP EMISSIONS; BOUNDARY-LAYER;
D O I
10.1016/j.scitotenv.2021.150928
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The impacts of natural dimethyl sulfide (DMS) and ship emissions on marine environments and particulate matter (PM) over the western and southern sea areas around South Korea were studied based on field campaigns from August-September 2017 and May-June 2018 using the Community Multi-scale Air Quality v5.3.2 modeling system. DMS oxidation enhanced the concentrations of both sulfur dioxide (SO2) and sulfate (SO42-) in PM2.5 by 6.2-6.4% and 2.9-3.6%, respectively, in the marine atmosphere during the study period, whereas it slightly decreased nitrate (NO3-) concentrations (by -1.3%), compared to the simulation without DMS oxidation chemistry. Furthermore, ship emissions increased the concentrations of SO4 , NO3, and NH4 by 4.5%, 23%, and 7.3%, respectively. Methane sulfonic add concentration was 0.17 Jg m(3), suggesting the importance of the addition channel in the DMS oxidation pathway. The model simulation indicated that ship emissions in the target area contributed dominantly to non-sea-salt SO42- and the marine DMS emission source was non-negligible. The geographical distribution of PM toxicity (aerosol oxidative potential) was assessed in the marine atmosphere during the study period. (C) 2021 Elsevier B.V. All rights reserved.
引用
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页数:14
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