Jianyan Lu , Chunhong Zhou , Jian Zhang , Lei Zhang , Shuhua Lu , Sunling Gong
{"title":"云化学对中国硫酸盐及其前体物季节变化的影响","authors":"Jianyan Lu , Chunhong Zhou , Jian Zhang , Lei Zhang , Shuhua Lu , Sunling Gong","doi":"10.1016/j.atmosenv.2024.120820","DOIUrl":null,"url":null,"abstract":"<div><div>Cloud chemistry is of paramount importance in the secondary production of atmospheric aerosols, influencing the spatial-temporal distribution of gases and aerosols in the atmosphere. Using WRF/CUACE (China Meteorological Administration Unified Atmospheric Chemistry Environment), this study assesses the seasonal impacts of cloud chemistry on the concentrations of SO<sub>2</sub>, sulfate, as well as two oxidizers, H<sub>2</sub>O<sub>2</sub> and O<sub>3</sub>, in the most east-central areas of China, including four key pollution zones (the North China Plain (NCP), the Yangtze River Delta (YRD), the Pearl River Delta (PRD), and the Sichuan Basin (SCB)). Near the surface, H<sub>2</sub>O<sub>2</sub>-oxidation was the dominant pathway for cloud chemistry in four key pollution zones in four seasons. H<sub>2</sub>O<sub>2</sub> consumption is most pronounced in summer, especially in the SCB and NCP, while O<sub>3</sub> consumption peaks in autumn, particularly in the PRD and southeastern coastal areas. While at higher altitudes, oxidation by O<sub>3</sub> and H<sub>2</sub>O<sub>2</sub> is compatible with the cloud chemistry process. Near the surface, cloud chemistry consumes SO<sub>2</sub> ranging from approximately 0.1 ppb–5.0 ppb, resulting in the generation of about 6.0–25.0 μg m<sup>−3</sup> of sulfate. Higher SO<sub>2</sub> reduction and sulfate increase are in both summer and winter, especially for the SCB and NCP in summer, and the SCB in winter. Vertically, the cloud chemistry process primarily concentrates its influence on SO<sub>2</sub> and sulfate concentrations below 5 km, particularly within the turbulent zone of the troposphere below 2 km in all the four pollution zones and four seasons. The most notable seasonal variation occurs in the NCP compared to other zones. This study also shows that cloud chemistry effectively improves the seasonal simulation accuracy of SO<sub>2</sub> and sulfate, resulting in improved correlation and a notable reduction in RMSE.</div></div>","PeriodicalId":250,"journal":{"name":"Atmospheric Environment","volume":"338 ","pages":"Article 120820"},"PeriodicalIF":4.2000,"publicationDate":"2024-09-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Effect of cloud chemistry on seasonal variations of sulfate and its precursors in China\",\"authors\":\"Jianyan Lu , Chunhong Zhou , Jian Zhang , Lei Zhang , Shuhua Lu , Sunling Gong\",\"doi\":\"10.1016/j.atmosenv.2024.120820\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Cloud chemistry is of paramount importance in the secondary production of atmospheric aerosols, influencing the spatial-temporal distribution of gases and aerosols in the atmosphere. Using WRF/CUACE (China Meteorological Administration Unified Atmospheric Chemistry Environment), this study assesses the seasonal impacts of cloud chemistry on the concentrations of SO<sub>2</sub>, sulfate, as well as two oxidizers, H<sub>2</sub>O<sub>2</sub> and O<sub>3</sub>, in the most east-central areas of China, including four key pollution zones (the North China Plain (NCP), the Yangtze River Delta (YRD), the Pearl River Delta (PRD), and the Sichuan Basin (SCB)). Near the surface, H<sub>2</sub>O<sub>2</sub>-oxidation was the dominant pathway for cloud chemistry in four key pollution zones in four seasons. H<sub>2</sub>O<sub>2</sub> consumption is most pronounced in summer, especially in the SCB and NCP, while O<sub>3</sub> consumption peaks in autumn, particularly in the PRD and southeastern coastal areas. While at higher altitudes, oxidation by O<sub>3</sub> and H<sub>2</sub>O<sub>2</sub> is compatible with the cloud chemistry process. Near the surface, cloud chemistry consumes SO<sub>2</sub> ranging from approximately 0.1 ppb–5.0 ppb, resulting in the generation of about 6.0–25.0 μg m<sup>−3</sup> of sulfate. Higher SO<sub>2</sub> reduction and sulfate increase are in both summer and winter, especially for the SCB and NCP in summer, and the SCB in winter. Vertically, the cloud chemistry process primarily concentrates its influence on SO<sub>2</sub> and sulfate concentrations below 5 km, particularly within the turbulent zone of the troposphere below 2 km in all the four pollution zones and four seasons. The most notable seasonal variation occurs in the NCP compared to other zones. This study also shows that cloud chemistry effectively improves the seasonal simulation accuracy of SO<sub>2</sub> and sulfate, resulting in improved correlation and a notable reduction in RMSE.</div></div>\",\"PeriodicalId\":250,\"journal\":{\"name\":\"Atmospheric Environment\",\"volume\":\"338 \",\"pages\":\"Article 120820\"},\"PeriodicalIF\":4.2000,\"publicationDate\":\"2024-09-18\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Atmospheric Environment\",\"FirstCategoryId\":\"93\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S1352231024004953\",\"RegionNum\":2,\"RegionCategory\":\"环境科学与生态学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"ENVIRONMENTAL SCIENCES\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Atmospheric Environment","FirstCategoryId":"93","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1352231024004953","RegionNum":2,"RegionCategory":"环境科学与生态学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"ENVIRONMENTAL SCIENCES","Score":null,"Total":0}
Effect of cloud chemistry on seasonal variations of sulfate and its precursors in China
Cloud chemistry is of paramount importance in the secondary production of atmospheric aerosols, influencing the spatial-temporal distribution of gases and aerosols in the atmosphere. Using WRF/CUACE (China Meteorological Administration Unified Atmospheric Chemistry Environment), this study assesses the seasonal impacts of cloud chemistry on the concentrations of SO2, sulfate, as well as two oxidizers, H2O2 and O3, in the most east-central areas of China, including four key pollution zones (the North China Plain (NCP), the Yangtze River Delta (YRD), the Pearl River Delta (PRD), and the Sichuan Basin (SCB)). Near the surface, H2O2-oxidation was the dominant pathway for cloud chemistry in four key pollution zones in four seasons. H2O2 consumption is most pronounced in summer, especially in the SCB and NCP, while O3 consumption peaks in autumn, particularly in the PRD and southeastern coastal areas. While at higher altitudes, oxidation by O3 and H2O2 is compatible with the cloud chemistry process. Near the surface, cloud chemistry consumes SO2 ranging from approximately 0.1 ppb–5.0 ppb, resulting in the generation of about 6.0–25.0 μg m−3 of sulfate. Higher SO2 reduction and sulfate increase are in both summer and winter, especially for the SCB and NCP in summer, and the SCB in winter. Vertically, the cloud chemistry process primarily concentrates its influence on SO2 and sulfate concentrations below 5 km, particularly within the turbulent zone of the troposphere below 2 km in all the four pollution zones and four seasons. The most notable seasonal variation occurs in the NCP compared to other zones. This study also shows that cloud chemistry effectively improves the seasonal simulation accuracy of SO2 and sulfate, resulting in improved correlation and a notable reduction in RMSE.
期刊介绍:
Atmospheric Environment has an open access mirror journal Atmospheric Environment: X, sharing the same aims and scope, editorial team, submission system and rigorous peer review.
Atmospheric Environment is the international journal for scientists in different disciplines related to atmospheric composition and its impacts. The journal publishes scientific articles with atmospheric relevance of emissions and depositions of gaseous and particulate compounds, chemical processes and physical effects in the atmosphere, as well as impacts of the changing atmospheric composition on human health, air quality, climate change, and ecosystems.