Sainan Wang, Mike J. Newland, Andrew R. Rickard, Jacqueline F. Hamilton, Thomas J. Bannan, Archit Mehra, Carl J. Percival, Freya A. Squires, Weiwei Hu, Wei Song, Yang Chen, Xiaoling Zhang, Liming Wang, Xinming Wang
{"title":"在城市地区通过高no氧化途径产生的异戊二烯环氧二醇(IEPOX)被严重低估","authors":"Sainan Wang, Mike J. Newland, Andrew R. Rickard, Jacqueline F. Hamilton, Thomas J. Bannan, Archit Mehra, Carl J. Percival, Freya A. Squires, Weiwei Hu, Wei Song, Yang Chen, Xiaoling Zhang, Liming Wang, Xinming Wang","doi":"10.1038/s41612-025-01151-4","DOIUrl":null,"url":null,"abstract":"<p>Isoprene is the dominant nonmethane volatile organic compound (VOC) emitted into the atmosphere globally, with important atmospheric chemistry impacts on air quality and climate. One crucial intermediate in its gas-phase oxidation is isoprene epoxydiol (IEPOX), which contributes significantly to the formation of secondary organic aerosols (SOA). It is generally accepted that IEPOX is efficiently formed in remote forested regions with a sufficiently low NO/HO<sub>2</sub> ratio. Here, we show that the oxidation of isoprene hydroxynitrates (IHN) can be an alternative, efficient, NO-driven pathway leading to the formation of IEPOX in urban areas where moderate to high NO concentrations exist. Field measurements from the megacity of Beijing show that this pathway contributes to more than 50% of IEPOX production during the morning and early afternoon. The results improve our understanding of the NO<sub>x</sub> dependence of SOA formation in polluted areas, where anthropogenic emissions can significantly enhance biogenic SOA formation.</p>","PeriodicalId":19438,"journal":{"name":"npj Climate and Atmospheric Science","volume":"4 1","pages":""},"PeriodicalIF":8.5000,"publicationDate":"2025-07-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Largely underestimated production of isoprene epoxydiols (IEPOX) through high-NO oxidation pathways in urban areas\",\"authors\":\"Sainan Wang, Mike J. Newland, Andrew R. Rickard, Jacqueline F. Hamilton, Thomas J. Bannan, Archit Mehra, Carl J. Percival, Freya A. Squires, Weiwei Hu, Wei Song, Yang Chen, Xiaoling Zhang, Liming Wang, Xinming Wang\",\"doi\":\"10.1038/s41612-025-01151-4\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>Isoprene is the dominant nonmethane volatile organic compound (VOC) emitted into the atmosphere globally, with important atmospheric chemistry impacts on air quality and climate. One crucial intermediate in its gas-phase oxidation is isoprene epoxydiol (IEPOX), which contributes significantly to the formation of secondary organic aerosols (SOA). It is generally accepted that IEPOX is efficiently formed in remote forested regions with a sufficiently low NO/HO<sub>2</sub> ratio. Here, we show that the oxidation of isoprene hydroxynitrates (IHN) can be an alternative, efficient, NO-driven pathway leading to the formation of IEPOX in urban areas where moderate to high NO concentrations exist. Field measurements from the megacity of Beijing show that this pathway contributes to more than 50% of IEPOX production during the morning and early afternoon. The results improve our understanding of the NO<sub>x</sub> dependence of SOA formation in polluted areas, where anthropogenic emissions can significantly enhance biogenic SOA formation.</p>\",\"PeriodicalId\":19438,\"journal\":{\"name\":\"npj Climate and Atmospheric Science\",\"volume\":\"4 1\",\"pages\":\"\"},\"PeriodicalIF\":8.5000,\"publicationDate\":\"2025-07-05\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"npj Climate and Atmospheric Science\",\"FirstCategoryId\":\"89\",\"ListUrlMain\":\"https://doi.org/10.1038/s41612-025-01151-4\",\"RegionNum\":1,\"RegionCategory\":\"地球科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"METEOROLOGY & ATMOSPHERIC SCIENCES\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"npj Climate and Atmospheric Science","FirstCategoryId":"89","ListUrlMain":"https://doi.org/10.1038/s41612-025-01151-4","RegionNum":1,"RegionCategory":"地球科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"METEOROLOGY & ATMOSPHERIC SCIENCES","Score":null,"Total":0}
Largely underestimated production of isoprene epoxydiols (IEPOX) through high-NO oxidation pathways in urban areas
Isoprene is the dominant nonmethane volatile organic compound (VOC) emitted into the atmosphere globally, with important atmospheric chemistry impacts on air quality and climate. One crucial intermediate in its gas-phase oxidation is isoprene epoxydiol (IEPOX), which contributes significantly to the formation of secondary organic aerosols (SOA). It is generally accepted that IEPOX is efficiently formed in remote forested regions with a sufficiently low NO/HO2 ratio. Here, we show that the oxidation of isoprene hydroxynitrates (IHN) can be an alternative, efficient, NO-driven pathway leading to the formation of IEPOX in urban areas where moderate to high NO concentrations exist. Field measurements from the megacity of Beijing show that this pathway contributes to more than 50% of IEPOX production during the morning and early afternoon. The results improve our understanding of the NOx dependence of SOA formation in polluted areas, where anthropogenic emissions can significantly enhance biogenic SOA formation.
期刊介绍:
npj Climate and Atmospheric Science is an open-access journal encompassing the relevant physical, chemical, and biological aspects of atmospheric and climate science. The journal places particular emphasis on regional studies that unveil new insights into specific localities, including examinations of local atmospheric composition, such as aerosols.
The range of topics covered by the journal includes climate dynamics, climate variability, weather and climate prediction, climate change, ocean dynamics, weather extremes, air pollution, atmospheric chemistry (including aerosols), the hydrological cycle, and atmosphere–ocean and atmosphere–land interactions. The journal welcomes studies employing a diverse array of methods, including numerical and statistical modeling, the development and application of in situ observational techniques, remote sensing, and the development or evaluation of new reanalyses.