{"title":"Continental pollutants modulate organic nitrogen and light absorption of marine organic aerosols over East Asian marginal seas","authors":"Chao Yu,Lin Zheng,Yujue Wang,Meijing Guo,Xu Yu,Yuqi Guo,Sisi Song,Kyoung-Soon Jang,Xiaohong Yao,Jian Zhen Yu,Huiwang Gao","doi":"10.5194/acp-26-13175-2026","DOIUrl":null,"url":null,"abstract":"Organic nitrogen (ON) in marine aerosols is not only an important fraction of atmospheric nitrogen deposition but also a vital contributor to light-absorbing organic aerosols. However, observational evidence is lacking on the driving factors of ON formation or its role in organic aerosol absorption, especially in marine atmosphere. Here, shipboard observations were conducted in spring, summer, and autumn over the Yellow Sea and Bohai Sea (YBS) to understand the spatiotemporal distributions and sources of aerosol ON over East Asian marginal seas. Aerosol ON was 0.35 ± 0.25 µg N m −3 , accounting for 4 %–60 % of total nitrogen across seasons. Concentrations of ON were the highest in autumn due to severe impacts of anthropogenic pollutants, followed by those in spring and summer. Anthropogenic secondary pollutants (aged biomass burning and secondary nitrate formation) contributed 36 %–76 % of ON, 46 %–83 % of water-soluble ON, and 39 %–89 % of water-insoluble ON. In spring, 55 % of ON, 45 % of water-soluble ON, and 54 % of water-insoluble ON were attributed to dust, and its contribution increased to > 80 % during a dust episode. In summer, marine sources associated with biological activity were important for aerosol ON formation. Nitrogen-containing organic compounds played vital roles in regulating light absorption by organic aerosols over the YBS. Elevated organic aerosol absorption was attributed not only to higher ON concentrations but also to increased absorption capability at higher ON / OC ratios. Our results highlight that transported continental ON drove the light absorption by marine organic aerosols over marginal seas.","PeriodicalId":8611,"journal":{"name":"Atmospheric Chemistry and Physics","volume":"55 1","pages":"13175-13188"},"PeriodicalIF":5.7000,"publicationDate":"2026-09-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Atmospheric Chemistry and Physics","FirstCategoryId":"89","ListUrlMain":"https://doi.org/10.5194/acp-26-13175-2026","RegionNum":1,"RegionCategory":"地球科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"ENVIRONMENTAL SCIENCES","Score":null,"Total":0}
引用次数: 0
Abstract
Organic nitrogen (ON) in marine aerosols is not only an important fraction of atmospheric nitrogen deposition but also a vital contributor to light-absorbing organic aerosols. However, observational evidence is lacking on the driving factors of ON formation or its role in organic aerosol absorption, especially in marine atmosphere. Here, shipboard observations were conducted in spring, summer, and autumn over the Yellow Sea and Bohai Sea (YBS) to understand the spatiotemporal distributions and sources of aerosol ON over East Asian marginal seas. Aerosol ON was 0.35 ± 0.25 µg N m −3 , accounting for 4 %–60 % of total nitrogen across seasons. Concentrations of ON were the highest in autumn due to severe impacts of anthropogenic pollutants, followed by those in spring and summer. Anthropogenic secondary pollutants (aged biomass burning and secondary nitrate formation) contributed 36 %–76 % of ON, 46 %–83 % of water-soluble ON, and 39 %–89 % of water-insoluble ON. In spring, 55 % of ON, 45 % of water-soluble ON, and 54 % of water-insoluble ON were attributed to dust, and its contribution increased to > 80 % during a dust episode. In summer, marine sources associated with biological activity were important for aerosol ON formation. Nitrogen-containing organic compounds played vital roles in regulating light absorption by organic aerosols over the YBS. Elevated organic aerosol absorption was attributed not only to higher ON concentrations but also to increased absorption capability at higher ON / OC ratios. Our results highlight that transported continental ON drove the light absorption by marine organic aerosols over marginal seas.
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.