Spatiotemporal distributions and oceanic emissions of short-lived halocarbons in the East China Sea

被引:2
作者
Qi, Qian-Qian [1 ]
Yang, Gui-Peng [1 ,2 ]
Yang, Bin [3 ]
He, Zhen [1 ,2 ,4 ]
机构
[1] Ocean Univ China, Frontiers Sci Ctr Deep Ocean Multispheres & Earth, Key Lab Marine Chem Theory & Technol, Coll Chem & Chem Engn,Minist Educ, Qingdao 266100, Peoples R China
[2] Qingdao Natl Lab Marine Sci & Technol, Lab Marine Ecol & Environm Sci, Qingdao 266237, Peoples R China
[3] Beibu Gulf Univ, Guangxi Key Lab Marine Environm Change & Disaster, Qinzhou 535011, Peoples R China
[4] Ocean Univ China, Key Lab Marine Chem Theory & Technol, Minist Educ, Qingdao 266100, Peoples R China
基金
中国国家自然科学基金;
关键词
Short-lived halocarbons; Spatiotemporal distributions; Oceanic emissions; East China Sea; VOLATILE HALOCARBONS; METHYL-IODIDE; OZONE DEPLETION; YELLOW SEA; BROMOFORM; SEAWATER; IMPACT; CHBR3; SEDIMENTS; DECLINE;
D O I
10.1016/j.scitotenv.2023.164879
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Coastal waters are important sources of volatile halocarbons, which are important in atmospheric chemistry. Here, in May (spring) and October (autumn) 2020, we studied the surface, bottom, and sediment-pore seawater concentrations, atmospheric mixing ratios, and sea-to-air fluxes of the three primary short-lived atmospheric halocarbons (CH3I, CH2Br2, and CHBr3) in the East China Sea (ECS). The highest concentrations of the three short-lived halocarbons oc-curred in coastal waters, such as the Changjiang estuary and Zhejiang coastal waters, reflecting the influence of exces-sive anthropogenic inputs on the distributions of these gases. Interestingly, the aqueous levels of these gases seemed to be lower compared to previous measurements in this oceanic region, probably due to reduced contributions from local anthropogenic emission sources. The concentrations of CH3I, CH2Br2, and CHBr3 in pore water were significantly higher than those in bottom water, suggesting that sediment could be a source of these short-lived halocarbons. Addi-tionally, the atmospheric mixing ratios of these gases occasionally increased in coastal areas. An air-mass back trajec-tory analysis showed this was due to continental anthropogenic sources and emissions from enriched waters. The atmospheric mixing ratios of these halocarbons exhibited significant seasonal variability, with significant correlations among atmospheric CH3I, CH2Br2, and CHBr3 in spring, but not in autumn. The sea-to-air fluxes of CH3I, CH2Br2, and CHBr3 indicated that the ECS is a source of these gases. Seasonal differences in CH3I and CH2Br2 fluxes were driven by changes in wind speed and sea surface temperature, while CHBr3 flux changes were associated with changes in its sur-face seawater concentration.
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页数:13
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