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Submicron Organic Aerosol Types in the Summertime Arctic: Mixing State, Geographic Distribution, and Drivers
Su, Bojiang1,2; Zhang, Guohua1,3; Song, Congbo4; Liang, Yue5; Wang, Longqun6; Li, Lei7; Zhou, Zhen7; Yan, Jinpei8; Wang, Xinming1,3; Bi, Xinhui1,3
2024-09-16
Source PublicationJournal of Geophysical Research: Atmospheres
ISSN2169-897X
Volume129Issue:17Pages:e2024JD041061
Abstract

During the 2017 summertime Arctic cruise observation campaigns, we measured over 290,000 individual submicron particles and clustered them into two inorganic classes (dominated by sea salt, accounting for 38.6% by number fraction) and five organic classes (dominated by natural and anthropogenic organics, 61.4%), presenting a distinct difference in geographic distribution. In the high Arctic and marginal ice zone (81.1–84.6°N) compared with the low Arctic (Chukchi Sea, Svalbard, and Iceland, <80°N), ocean-derived organic aerosols were more prevalent (73.6% vs. 37.1%). Specifically, we found sharp contrasts in the geographic distributions of OC-Ca (organics internally mixed with calcium, 29.0% vs. 9.4%) and OC-S (organics internally mixed with sulfate, 3.2% vs. 21.4%). Utilizing an explainable machine learning technique, we inferred that OC-Ca was driven by wind-blown sea ice and/or sea ice floes and/or bubble bursting within sea ice leads under low wind speed conditions in the high Arctic, while OC-S tended to associate with elemental carbon, sulfate, and higher temperatures, potentially originating from combustion emissions at low latitude regions.

Other Abstract

Plain Language Summary

Knowledge of the mixing state of individual particles is essential for elucidating their sources, formation mechanisms, atmospheric processes, and assessing their climate effect in the Arctic atmosphere. Here, we investigated the origins and geographic distribution of organic aerosol types using a single-particle aerosol mass spectrometer during the 8th Chinese Arctic Expedition Research Cruise (Chinese Research Vessel Xuelong) in the summertime over the Arctic Ocean. According to the mixing state, individual organic particles were classified into several ocean-derived and anthropogenic types. Ocean-derived types were prevalent in the high Arctic compared with that of anthropogenic type in the low Arctic, and their driven factors were different. Specifically, sea ice fraction was the most important driver for the generation of ocean-derived OC-Ca (an aerosol type of organics internally mixed with calcium). OC-S (an aerosol type of organics internally mixed with sulfate) substantially increased in the low Arctic, most probably driven by combustion sources. 

KeywordDriver Geographic Distribution Individual Organic Aerosol Particles Machine Learning Mixing State Summertime High Arctic
DOI10.1029/2024JD041061
URLView the original
Indexed BySCIE
Language英語English
WOS Research AreaMeteorology & Atmospheric Sciences
WOS SubjectMeteorology & Atmospheric Sciences
WOS IDWOS:001309876500001
PublisherAMER GEOPHYSICAL UNION, 2000 FLORIDA AVE NW, WASHINGTON, DC 20009
Scopus ID2-s2.0-85203401451
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Citation statistics
Document TypeJournal article
CollectionFaculty of Science and Technology
DEPARTMENT OF CIVIL AND ENVIRONMENTAL ENGINEERING
Corresponding AuthorZhang, Guohua; Bi, Xinhui
Affiliation1.State Key Laboratory of Organic Geochemistry and Guangdong Provincial Key Laboratory of Environmental Protection and Resources Utilization, Guangzhou Institute of Geochemistry, Chinese Academy of Sciences, Guangzhou, China
2.University of Chinese Academy of Sciences, Beijing, China
3.Guangdong-Hong Kong-Macao Joint Laboratory for Environmental Pollution and Control, Guangzhou, China
4.National Centre for Atmospheric Science (NCAS), The University of Manchester, Manchester, United Kingdom
5.Department of Civil and Environmental Engineering, Faculty of Science and Technology, University of Macau, Macao
6.Anhui Key Laboratory of Polar Environment and Global Change, Department of Environmental Science and Engineering, University of Science and Technology of China, Hefei, China
7.Institute of Mass Spectrometry and Atmospheric Environment, Jinan University, Guangzhou, China
8.Key Laboratory of Global Change and Marine–Atmospheric Chemistry, Third Institute of Oceanography, Ministry of Natural Resources, Xiamen, China
Recommended Citation
GB/T 7714
Su, Bojiang,Zhang, Guohua,Song, Congbo,et al. Submicron Organic Aerosol Types in the Summertime Arctic: Mixing State, Geographic Distribution, and Drivers[J]. Journal of Geophysical Research: Atmospheres, 2024, 129(17), e2024JD041061.
APA Su, Bojiang., Zhang, Guohua., Song, Congbo., Liang, Yue., Wang, Longqun., Li, Lei., Zhou, Zhen., Yan, Jinpei., Wang, Xinming., & Bi, Xinhui (2024). Submicron Organic Aerosol Types in the Summertime Arctic: Mixing State, Geographic Distribution, and Drivers. Journal of Geophysical Research: Atmospheres, 129(17), e2024JD041061.
MLA Su, Bojiang,et al."Submicron Organic Aerosol Types in the Summertime Arctic: Mixing State, Geographic Distribution, and Drivers".Journal of Geophysical Research: Atmospheres 129.17(2024):e2024JD041061.
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