| 1. |
- Adachi, Kouji, et al.
(author)
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Composition and mixing state of Arctic aerosol and cloud residual particles from long-term sinale-particle observations at Zeppelin Observatory, Svalbard
- 2022
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In: Atmospheric Chemistry And Physics. - : Copernicus GmbH. - 1680-7316 .- 1680-7324. ; 22:21, s. 14421-14439
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Journal article (peer-reviewed)abstract
- 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-Ålesund, 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, K-bearing, 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 ∘C. On the other hand, cloud residual samples collected at ambient temperatures below 0 ∘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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| 2. |
- Adachi, Kouji, et al.
(author)
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Composition and mixing state of individual aerosol particles from northeast Greenland and Svalbard in the Arctic during spring 2018
- 2023
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In: Atmospheric Environment. - 1352-2310 .- 1873-2844. ; 314
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Journal article (peer-reviewed)abstract
- The Arctic region is warming about four times faster than the rest of the globe, and thus it is important to understand the processes driving climate change in this region. Aerosols are a significant component of the Arctic climate system as they form ice crystals and liquid droplets that control the dynamics of clouds and also directly interact with solar radiation, depending on the compositions and mixing states of individual particles. Here, we report on the characteristics of submicron-sized aerosol particles using transmission electron microscopy obtained at two high Arctic sites, northeast Greenland (Villum Research Station) and Svalbard (Zeppelin Observatory), during spring 2018. The results showed that a dominant compound in the submicron-sized spring aerosols was sulfate, followed by sea salt particles. Both model simulations and observations at the Zeppelin Observatory showed that sea salt particles became more prevalent when low-pressure systems passed by the station. Model simulations indicate that both sampling sites were affected by diffused and diluted long-range transport of anthropogenic aerosols from lower latitudes with negligible influences of biomass burning emissions during the observation period. Overall, the composition of measured aerosol particles from the two Arctic sites was generally similar and showed no apparent variation except for the sea salt fractions. This study shows a general picture of high Arctic aerosol particles influenced by marine sources and diffused long-range transport of anthropogenic sources during the Arctic spring period. These results will contribute to a better knowledge of the aerosol composition and mixing state during the Arctic spring, which helps to understand the contributions of aerosols to the Arctic climate.
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| 3. |
- Pereira Freitas, Gabriel, 1993-, et al.
(author)
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Contribution of primary biological aerosol particles to low-level Arctic cloud condensation nuclei
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Other publication (other academic/artistic)abstract
- Mixed-phase clouds (MPC) are key players in the Arctic climate system due to their role in modulating solar and terrestrial radiation. Such radiative interactions critically rely on the ice content of MPC which, in turn, partly depends on the availability of ice nucleating particles (INP). INP sources and concentrations are poorly understood in the Arctic. Recently, INP active at high temperatures were linked to be primary biological aerosol particles (PBAP). Here, we investigated for a full year the PBAP abundance and variability within cloud residuals, directly sampled by a multiparameter bioaerosol spectrometer coupled to a ground-based counterflow virtual impactor inlet at the Zeppelin Observatory (475 m asl), Ny-Ålesund, Svalbard. PBAP concentrations (10−3–10−2L−1) and contributions to coarse-mode aerosol (1 in every 103–104) within cloud residuals were found to be close to those expected for concentrations of high-temperature INP. Transmission electron microscopy also confirmed the presence of PBAP, most likely bacteria, within the cloud residual samples. Seasonally, our results reveal an elevated presence of PBAP within cloud residuals during the summer. Parallel water vapor isotope measurements points towards a link between summer clouds and regionally sourced air masses. Low-level MPC were predominantly observed at the beginning and end of summer, and one explanation for their presence is the existence of high-temperature INP. In this study, we present observational evidence that PBAP might play a role in determining the phase of low-level Arctic clouds, with potential implications for the Arctic climate given ongoing changes in the hydrological and biogeochemical cycles that influence the PBAP flux in and towards the Arctic.
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| 4. |
- Pereira Freitas, Gabriel, 1993-, et al.
(author)
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Regionally sourced bioaerosols drive high-temperature ice nucleating particles in the Arctic
- 2023
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In: Nature Communications. - 2041-1723. ; 14
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Journal article (peer-reviewed)abstract
- Primary biological aerosol particles (PBAP) play an important role in the climate system, facilitating the formation of ice within clouds, consequently PBAP may be important in understanding the rapidly changing Arctic. Within this work, we use single-particle fluorescence spectroscopy to identify and quantify PBAP at an Arctic mountain site, with transmission electronic microscopy analysis supporting the presence of PBAP. We find that PBAP concentrations range between 10−3–10−1 L−1 and peak in summer. Evidences suggest that the terrestrial Arctic biosphere is an important regional source of PBAP, given the high correlation to air temperature, surface albedo, surface vegetation and PBAP tracers. PBAP clearly correlate with high-temperature ice nucleating particles (INP) (>-15 °C), of which a high a fraction (>90%) are proteinaceous in summer, implying biological origin. These findings will contribute to an improved understanding of sources and characteristics of Arctic PBAP and their links to INP.
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