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DOI | 10.5194/acp-22-14421-2022 |
Composition and mixing state of Arctic aerosol and cloud residual particles from long-term sinale-particle observations at Zeppelin Observatory, Svalbard | |
Adachi, Kouji; Tobo, Yutaka; Koike, Makoto; Freitas, Gabriel; Zieger, Paul; Krejci, Radovan | |
发表日期 | 2022 |
ISSN | 1680-7316 |
EISSN | 1680-7324 |
起始页码 | 14421 |
结束页码 | 14439 |
卷号 | 22期号:21页码:19 |
英文摘要 | The Arctic region is sensitive to climate change and is warming faster than the global average. Aerosol particles change cloud properties by acting as cloud condensation nuclei and ice-nucleating particles, thus influencing the Arctic climate system. Therefore, understanding the aerosol particle properties in the Arctic is needed to interpret and simulate their influences on climate. In this study, we collected ambient aerosol particles using whole-air and PM10 inlets and residual particles of cloud droplets and ice crystals from Arctic low-level clouds (typically, all-liquid or mixed-phase clouds) using a counterflow virtual impactor inlet at the Zeppelin Observatory near Ny-Alesund, Svalbard, within a time frame of 4 years. We measured the composition and mixing state of individual fine-mode particles in 239 samples using transmission electron microscopy. On the basis of their composition, the aerosol and cloud residual particles were classified as mineral dust, sea salt, Kbearing, sulfate, and carbonaceous particles. The number fraction of aerosol particles showed seasonal changes, with sulfate dominating in summer and sea salt increasing in winter. There was no measurable difference in the fractions between ambient aerosol and cloud residual particles collected at ambient temperatures above 0 degrees C. On the other hand, cloud residual samples collected at ambient temperatures below 0 degrees C had several times more sea salt and mineral dust particles and fewer sulfates than ambient aerosol samples, suggesting that sea spray and mineral dust particles may influence the formation of cloud particles in Arctic mixed-phase clouds. We also found that 43 % of mineral dust particles from cloud residual samples were mixed with sea salt, whereas only 18 % of mineral dust particles in ambient aerosol samples were mixed with sea salt. This study highlights the variety in aerosol compositions and mixing states that influence or are influenced by aerosol-cloud interactions in Arctic low-level clouds. |
学科领域 | Environmental Sciences; Meteorology & Atmospheric Sciences |
语种 | 英语 |
WOS研究方向 | Environmental Sciences & Ecology ; Meteorology & Atmospheric Sciences |
WOS记录号 | WOS:000880659800001 |
来源期刊 | ATMOSPHERIC CHEMISTRY AND PHYSICS
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文献类型 | 期刊论文 |
条目标识符 | http://gcip.llas.ac.cn/handle/2XKMVOVA/273187 |
作者单位 | Meteorological Research Institute - Japan; Research Organization of Information & Systems (ROIS); National Institute of Polar Research (NIPR) - Japan; Graduate University for Advanced Studies - Japan; University of Tokyo; Stockholm University; Stockholm University |
推荐引用方式 GB/T 7714 | Adachi, Kouji,Tobo, Yutaka,Koike, Makoto,et al. Composition and mixing state of Arctic aerosol and cloud residual particles from long-term sinale-particle observations at Zeppelin Observatory, Svalbard[J],2022,22(21):19. |
APA | Adachi, Kouji,Tobo, Yutaka,Koike, Makoto,Freitas, Gabriel,Zieger, Paul,&Krejci, Radovan.(2022).Composition and mixing state of Arctic aerosol and cloud residual particles from long-term sinale-particle observations at Zeppelin Observatory, Svalbard.ATMOSPHERIC CHEMISTRY AND PHYSICS,22(21),19. |
MLA | Adachi, Kouji,et al."Composition and mixing state of Arctic aerosol and cloud residual particles from long-term sinale-particle observations at Zeppelin Observatory, Svalbard".ATMOSPHERIC CHEMISTRY AND PHYSICS 22.21(2022):19. |
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