Yang Yang, Shaoxuan Mou, Hailong Wang, Pinya Wang, Baojie Li, Hong Liao
{"title":"1850-2017 年按主要排放区域和部门划分的全球气溶胶源分配情况","authors":"Yang Yang, Shaoxuan Mou, Hailong Wang, Pinya Wang, Baojie Li, Hong Liao","doi":"10.5194/egusphere-2023-2552","DOIUrl":null,"url":null,"abstract":"<strong>Abstract.</strong> Anthropogenic emissions of aerosols and precursor gases have been changing significantly in the past few decades across the world. In this study, an explicit aerosol source tagging system (EAST) is merged into the Energy Exascale Earth System Model version 1 (E3SMv1) to quantify the variations in anthropogenic aerosol concentrations, source contributions, and their subsequent radiative impact in four major emission regions on the globe during 1850–1980, 1980–2010 and 2010–2017. In North America and Europe, changes in anthropogenic PM<sub>2.5</sub> were mainly caused by changes in emissions from local energy and industrial sectors. The local industrial sector caused the most increase in PM<sub>2.5</sub> in East Asia during1980–2010 and decrease during 2010–2017. In South Asia, the increase in energy-related emissions dominated the rise of PM<sub>2.5</sub> levels during 1980–2017. During 1850–1980, the increases in emissions from North America contributed to the increase in European PM<sub>2.5</sub> burden by 1.7 mg m<sup>-2</sup> and the sources from the Europe were also responsible for the PM<sub>2.5</sub> burden increase in East Asia and South Asia by about 1.0 mg m<sup>-2</sup>. During 1980–2010, East Asia contributed to an increase of 0.4–0.6 mg m<sup>-2</sup> in PM<sub>2.5</sub> burden in North America and Europe, while South Asian contributed about 0.3 mg m<sup>-2</sup>. During 2010–2017, the contributions from East Asia to the PM<sub>2.5</sub> burdens in the North America, Europe and South Asia declined by 0.3–0.6 mg m<sup>-2</sup> due to Clean Air actions in China, while the contributions from South Asia still increased due to the continuous increase in emissions in South Asia. The historical changes in aerosols had an impact on effective radiative forcing through aerosol-radiation interactions (ERF<sub>ari</sub>). During 1980–2010, a decline in North American aerosols resulted in a positive ERF<sub>ari</sub> change (warming effect) in Europe and a decline of aerosols in Europe caused a warming effect in Russia and northern China. The changes in ERF<sub>ari</sub> from the increase and decrease of aerosols in China during 1980–2010 and 2010–2017, respectively, are comparable in magnitude. The continuous aerosol increases in South Asia from 1980 to 2017 resulted in negative ERF<sub>ari</sub> (cooling) changes in South Asia, Southeast Asia, and southern China.","PeriodicalId":8611,"journal":{"name":"Atmospheric Chemistry and Physics","volume":"10 1","pages":""},"PeriodicalIF":5.2000,"publicationDate":"2024-01-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Global source apportionment of aerosols into major emission regions and sectors over 1850–2017\",\"authors\":\"Yang Yang, Shaoxuan Mou, Hailong Wang, Pinya Wang, Baojie Li, Hong Liao\",\"doi\":\"10.5194/egusphere-2023-2552\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<strong>Abstract.</strong> Anthropogenic emissions of aerosols and precursor gases have been changing significantly in the past few decades across the world. In this study, an explicit aerosol source tagging system (EAST) is merged into the Energy Exascale Earth System Model version 1 (E3SMv1) to quantify the variations in anthropogenic aerosol concentrations, source contributions, and their subsequent radiative impact in four major emission regions on the globe during 1850–1980, 1980–2010 and 2010–2017. In North America and Europe, changes in anthropogenic PM<sub>2.5</sub> were mainly caused by changes in emissions from local energy and industrial sectors. The local industrial sector caused the most increase in PM<sub>2.5</sub> in East Asia during1980–2010 and decrease during 2010–2017. In South Asia, the increase in energy-related emissions dominated the rise of PM<sub>2.5</sub> levels during 1980–2017. During 1850–1980, the increases in emissions from North America contributed to the increase in European PM<sub>2.5</sub> burden by 1.7 mg m<sup>-2</sup> and the sources from the Europe were also responsible for the PM<sub>2.5</sub> burden increase in East Asia and South Asia by about 1.0 mg m<sup>-2</sup>. During 1980–2010, East Asia contributed to an increase of 0.4–0.6 mg m<sup>-2</sup> in PM<sub>2.5</sub> burden in North America and Europe, while South Asian contributed about 0.3 mg m<sup>-2</sup>. During 2010–2017, the contributions from East Asia to the PM<sub>2.5</sub> burdens in the North America, Europe and South Asia declined by 0.3–0.6 mg m<sup>-2</sup> due to Clean Air actions in China, while the contributions from South Asia still increased due to the continuous increase in emissions in South Asia. The historical changes in aerosols had an impact on effective radiative forcing through aerosol-radiation interactions (ERF<sub>ari</sub>). During 1980–2010, a decline in North American aerosols resulted in a positive ERF<sub>ari</sub> change (warming effect) in Europe and a decline of aerosols in Europe caused a warming effect in Russia and northern China. The changes in ERF<sub>ari</sub> from the increase and decrease of aerosols in China during 1980–2010 and 2010–2017, respectively, are comparable in magnitude. 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Global source apportionment of aerosols into major emission regions and sectors over 1850–2017
Abstract. Anthropogenic emissions of aerosols and precursor gases have been changing significantly in the past few decades across the world. In this study, an explicit aerosol source tagging system (EAST) is merged into the Energy Exascale Earth System Model version 1 (E3SMv1) to quantify the variations in anthropogenic aerosol concentrations, source contributions, and their subsequent radiative impact in four major emission regions on the globe during 1850–1980, 1980–2010 and 2010–2017. In North America and Europe, changes in anthropogenic PM2.5 were mainly caused by changes in emissions from local energy and industrial sectors. The local industrial sector caused the most increase in PM2.5 in East Asia during1980–2010 and decrease during 2010–2017. In South Asia, the increase in energy-related emissions dominated the rise of PM2.5 levels during 1980–2017. During 1850–1980, the increases in emissions from North America contributed to the increase in European PM2.5 burden by 1.7 mg m-2 and the sources from the Europe were also responsible for the PM2.5 burden increase in East Asia and South Asia by about 1.0 mg m-2. During 1980–2010, East Asia contributed to an increase of 0.4–0.6 mg m-2 in PM2.5 burden in North America and Europe, while South Asian contributed about 0.3 mg m-2. During 2010–2017, the contributions from East Asia to the PM2.5 burdens in the North America, Europe and South Asia declined by 0.3–0.6 mg m-2 due to Clean Air actions in China, while the contributions from South Asia still increased due to the continuous increase in emissions in South Asia. The historical changes in aerosols had an impact on effective radiative forcing through aerosol-radiation interactions (ERFari). During 1980–2010, a decline in North American aerosols resulted in a positive ERFari change (warming effect) in Europe and a decline of aerosols in Europe caused a warming effect in Russia and northern China. The changes in ERFari from the increase and decrease of aerosols in China during 1980–2010 and 2010–2017, respectively, are comparable in magnitude. The continuous aerosol increases in South Asia from 1980 to 2017 resulted in negative ERFari (cooling) changes in South Asia, Southeast Asia, and southern China.
期刊介绍:
Atmospheric Chemistry and Physics (ACP) is a not-for-profit international scientific journal dedicated to the publication and public discussion of high-quality studies investigating the Earth''s atmosphere and the underlying chemical and physical processes. It covers the altitude range from the land and ocean surface up to the turbopause, including the troposphere, stratosphere, and mesosphere.
The main subject areas comprise atmospheric modelling, field measurements, remote sensing, and laboratory studies of gases, aerosols, clouds and precipitation, isotopes, radiation, dynamics, biosphere interactions, and hydrosphere interactions. The journal scope is focused on studies with general implications for atmospheric science rather than investigations that are primarily of local or technical interest.