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二甲基硫化学对北半球空气质量的影响。

Impact of dimethylsulfide chemistry on air quality over the Northern Hemisphere.

作者信息

Zhao Junri, Sarwar Golam, Gantt Brett, Foley Kristen, Henderson Barron H, Pye Havala O T, Fahey Kathleen, Kang Daiwen, Mathur Rohit, Zhang Yan, Li Qinyi, Saiz-Lopez Alfonso

机构信息

Shanghai Key Laboratory of Atmospheric Particle Pollution and Prevention (LAP3), Department of Environmental Science and Engineering, Fudan University, Shanghai 200438, China.

Center for Environmental Measurement and Modeling, Office of Research and Development, U.S. Environmental Protection Agency, Research Triangle Park, North Carolina, USA.

出版信息

Atmos Environ (1994). 2020 Oct 29;244:117961. doi: 10.1016/j.atmosenv.2020.117961.

Abstract

We implement oceanic dimethylsulfide (DMS) emissions and its atmospheric chemical reactions into the Community Multiscale Air Quality (CMAQv53) model and perform annual simulations without and with DMS chemistry to quantify its impact on tropospheric composition and air quality over the Northern Hemisphere. DMS chemistry enhances both sulfur dioxide (SO) and sulfate ( ) over seawater and coastal areas. It enhances annual mean surface SO concentration by +46 pptv and by +0.33 μg/m and decreases aerosol nitrate concentration by -0.07 μg/m over seawater compared to the simulation without DMS chemistry. The changes decrease with altitude and are limited to the lower atmosphere. Impacts of DMS chemistry on are largest in the summer and lowest in the fall due to the seasonality of DMS emissions, atmospheric photochemistry and resultant oxidant levels. Hydroxyl and nitrate radical-initiated pathways oxidize 75% of the DMS while halogen-initiated pathways oxidize 25%. DMS chemistry leads to more acidic particles over seawater by decreasing aerosol pH. Increased from DMS enhances atmospheric extinction while lower aerosol nitrate reduces the extinction so that the net effect of DMS chemistry on visibility tends to remain unchanged over most of the seawater.

摘要

我们将海洋二甲基硫(DMS)排放及其大气化学反应纳入社区多尺度空气质量(CMAQv53)模型,并分别进行了不考虑和考虑DMS化学作用的年度模拟,以量化其对北半球对流层成分和空气质量的影响。DMS化学作用增强了海水和沿海地区的二氧化硫(SO)和硫酸盐( )。与不考虑DMS化学作用的模拟相比,它使海水区域的年平均地表SO浓度增加了+46 pptv, 增加了+0.33 μg/m,气溶胶硝酸盐浓度降低了-0.07 μg/m。这些变化随高度降低,且仅限于低层大气。由于DMS排放、大气光化学和由此产生的氧化剂水平的季节性变化,DMS化学作用对 的影响在夏季最大,秋季最小。羟基和硝酸根自由基引发的途径氧化了75%的DMS,而卤素引发的途径氧化了25%。DMS化学作用通过降低气溶胶pH值,使海水上方的颗粒更具酸性。DMS增加的 增强了大气消光,而较低的气溶胶硝酸盐降低了消光,因此在大多数海水区域,DMS化学作用对能见度的净影响往往保持不变。

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