4.7 Article

Composition and mixing state of Arctic aerosol and cloud residual particles from long-term sinale-particle observations at Zeppelin Observatory, Svalbard

期刊

ATMOSPHERIC CHEMISTRY AND PHYSICS
卷 22, 期 21, 页码 14421-14439

出版社

COPERNICUS GESELLSCHAFT MBH
DOI: 10.5194/acp-22-14421-2022

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资金

  1. Japan Society for the Promotion of Science [JP19H01972, JP19K21905, 19H04236, JP19H04259]
  2. Environment Research and Technology Development Fund of the Environmental Restoration and Conservation Agency of Japan [JPMEERF20205001, JPMEERF20202003, JPMEERF20215003, JPMEERF20172003]
  3. Global Environmental Research Co-ordination System of the Ministry of the Environment of Japan [MLIT1753]
  4. Arctic Challenge for Sustainability (ArCS) project [JPMXD1300000000]
  5. ArCS II project of the Ministry of Education, Culture, Sports, Science and Technology (MEXT) of Japan [JPMXD1420318865]
  6. Swedish Environmental Protection Agency (Naturvardsverket)
  7. Knut and Alice Wallenberg Foundation (KWA)
  8. FORMAS [2016-01427]
  9. Formas [2016-01427] Funding Source: Formas

向作者/读者索取更多资源

The Arctic region is sensitive to climate change and this study investigates the properties of aerosol particles in order to understand their impact on the Arctic climate system. The study found that the composition of aerosol particles varied with season, with sulfate dominating in summer and sea salt increasing in winter. Additionally, cloud residual samples collected at temperatures below 0 degrees C had more sea salt and mineral dust particles, suggesting their influence on cloud particle formation in Arctic mixed-phase clouds.
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.

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