Kaspar R. Daellenbach, Jing Cai, Simo Hakala, Lubna Dada, Chao Yan, Wei Du, Lei Yao, Feixue Zheng, Jialiang Ma, Florian Ungeheuer, Alexander L. Vogel, Dominik Stolzenburg, Yufang Hao, Yongchun Liu, Federico Bianchi, Gaëlle Uzu, Jean-Luc Jaffrezo, Douglas R. Worsnop, Neil M. Donahue, Markku Kulmala
{"title":"运输排放对北京有机气溶胶的贡献巨大","authors":"Kaspar R. Daellenbach, Jing Cai, Simo Hakala, Lubna Dada, Chao Yan, Wei Du, Lei Yao, Feixue Zheng, Jialiang Ma, Florian Ungeheuer, Alexander L. Vogel, Dominik Stolzenburg, Yufang Hao, Yongchun Liu, Federico Bianchi, Gaëlle Uzu, Jean-Luc Jaffrezo, Douglas R. Worsnop, Neil M. Donahue, Markku Kulmala","doi":"10.1038/s41561-024-01493-3","DOIUrl":null,"url":null,"abstract":"Haze in Beijing is linked to atmospherically formed secondary organic aerosol, which has been shown to be particularly harmful to human health. However, the sources and formation pathways of these secondary aerosols remain largely unknown, hindering effective pollution mitigation. Here we have quantified the sources of organic aerosol via direct near-molecular observations in central Beijing. In winter, organic aerosol pollution arises mainly from fresh solid-fuel emissions and secondary organic aerosols originating from both solid-fuel combustion and aqueous processes, probably involving multiphase chemistry with aromatic compounds. The most severe haze is linked to secondary organic aerosols originating from solid-fuel combustion, transported from the Beijing–Tianjing–Hebei Plain and rural mountainous areas west of Beijing. In summer, the increased fraction of secondary organic aerosol is dominated by aromatic emissions from the Xi’an–Shanghai–Beijing region, while the contribution of biogenic emissions remains relatively small. Overall, we identify the main sources of secondary organic aerosol affecting Beijing, which clearly extend beyond the local emissions in Beijing. Our results suggest that targeting key organic precursor emission sectors regionally may be needed to effectively mitigate organic aerosol pollution. Secondary organic aerosols in Beijing are driven by emissions from outside of the city, with seasonally different emission sources, according to molecular chemical characterization of particulate air pollution.","PeriodicalId":19053,"journal":{"name":"Nature Geoscience","volume":"17 8","pages":"747-754"},"PeriodicalIF":15.7000,"publicationDate":"2024-08-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.nature.com/articles/s41561-024-01493-3.pdf","citationCount":"0","resultStr":"{\"title\":\"Substantial contribution of transported emissions to organic aerosol in Beijing\",\"authors\":\"Kaspar R. Daellenbach, Jing Cai, Simo Hakala, Lubna Dada, Chao Yan, Wei Du, Lei Yao, Feixue Zheng, Jialiang Ma, Florian Ungeheuer, Alexander L. Vogel, Dominik Stolzenburg, Yufang Hao, Yongchun Liu, Federico Bianchi, Gaëlle Uzu, Jean-Luc Jaffrezo, Douglas R. Worsnop, Neil M. Donahue, Markku Kulmala\",\"doi\":\"10.1038/s41561-024-01493-3\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Haze in Beijing is linked to atmospherically formed secondary organic aerosol, which has been shown to be particularly harmful to human health. However, the sources and formation pathways of these secondary aerosols remain largely unknown, hindering effective pollution mitigation. Here we have quantified the sources of organic aerosol via direct near-molecular observations in central Beijing. In winter, organic aerosol pollution arises mainly from fresh solid-fuel emissions and secondary organic aerosols originating from both solid-fuel combustion and aqueous processes, probably involving multiphase chemistry with aromatic compounds. The most severe haze is linked to secondary organic aerosols originating from solid-fuel combustion, transported from the Beijing–Tianjing–Hebei Plain and rural mountainous areas west of Beijing. In summer, the increased fraction of secondary organic aerosol is dominated by aromatic emissions from the Xi’an–Shanghai–Beijing region, while the contribution of biogenic emissions remains relatively small. Overall, we identify the main sources of secondary organic aerosol affecting Beijing, which clearly extend beyond the local emissions in Beijing. Our results suggest that targeting key organic precursor emission sectors regionally may be needed to effectively mitigate organic aerosol pollution. 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Substantial contribution of transported emissions to organic aerosol in Beijing
Haze in Beijing is linked to atmospherically formed secondary organic aerosol, which has been shown to be particularly harmful to human health. However, the sources and formation pathways of these secondary aerosols remain largely unknown, hindering effective pollution mitigation. Here we have quantified the sources of organic aerosol via direct near-molecular observations in central Beijing. In winter, organic aerosol pollution arises mainly from fresh solid-fuel emissions and secondary organic aerosols originating from both solid-fuel combustion and aqueous processes, probably involving multiphase chemistry with aromatic compounds. The most severe haze is linked to secondary organic aerosols originating from solid-fuel combustion, transported from the Beijing–Tianjing–Hebei Plain and rural mountainous areas west of Beijing. In summer, the increased fraction of secondary organic aerosol is dominated by aromatic emissions from the Xi’an–Shanghai–Beijing region, while the contribution of biogenic emissions remains relatively small. Overall, we identify the main sources of secondary organic aerosol affecting Beijing, which clearly extend beyond the local emissions in Beijing. Our results suggest that targeting key organic precursor emission sectors regionally may be needed to effectively mitigate organic aerosol pollution. Secondary organic aerosols in Beijing are driven by emissions from outside of the city, with seasonally different emission sources, according to molecular chemical characterization of particulate air pollution.
期刊介绍:
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