Cloud condensation nuclei closure study on summer arctic aerosol

We present an aerosol – cloud condensation nuclei (CCN) closure study on summer high Arctic aerosol based on measurements that were carried out in 2008 during the Arctic Summer Cloud Ocean Study (ASCOS) on board the Swedish ice breaker Oden . The data presented here were collected during a three-wee...

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Published in:Atmospheric Chemistry and Physics
Main Authors: Martin, M., Chang, R. Y.-W., Sierau, B., Sjogren, S., Swietlicki, E., Abbatt, J. P. D., Leck, C., Lohmann, U.
Format: Text
Language:English
Published: 2018
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Online Access:https://doi.org/10.5194/acp-11-11335-2011
https://www.atmos-chem-phys.net/11/11335/2011/
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spelling ftcopernicus:oai:publications.copernicus.org:acp10604 2023-05-15T14:55:21+02:00 Cloud condensation nuclei closure study on summer arctic aerosol Martin, M. Chang, R. Y.-W. Sierau, B. Sjogren, S. Swietlicki, E. Abbatt, J. P. D. Leck, C. Lohmann, U. 2018-01-15 application/pdf https://doi.org/10.5194/acp-11-11335-2011 https://www.atmos-chem-phys.net/11/11335/2011/ eng eng doi:10.5194/acp-11-11335-2011 https://www.atmos-chem-phys.net/11/11335/2011/ eISSN: 1680-7324 Text 2018 ftcopernicus https://doi.org/10.5194/acp-11-11335-2011 2019-12-24T09:56:34Z We present an aerosol – cloud condensation nuclei (CCN) closure study on summer high Arctic aerosol based on measurements that were carried out in 2008 during the Arctic Summer Cloud Ocean Study (ASCOS) on board the Swedish ice breaker Oden . The data presented here were collected during a three-week time period in the pack ice (>85° N) when the icebreaker Oden was moored to an ice floe and drifted passively during the most biological active period into autumn freeze up conditions. CCN number concentrations were obtained using two CCN counters measuring at different supersaturations. The directly measured CCN number concentration was then compared with a CCN number concentration calculated using both bulk aerosol mass composition data from an aerosol mass spectrometer (AMS) and aerosol number size distributions obtained from a differential mobility particle sizer, assuming κ-Köhler theory, surface tension of water and an internally mixed aerosol. The last assumption was supported by measurements made with a hygroscopic tandem differential mobility analyzer (HTDMA) for particles >70 nm. For the two highest measured supersaturations, 0.73 and 0.41%, closure could not be achieved with the investigated settings concerning hygroscopicity and density. The calculated CCN number concentration was always higher than the measured one for those two supersaturations. This might be caused by a relative larger insoluble organic mass fraction of the smaller particles that activate at these supersaturations, which are thus less good CCN than the larger particles. On average, 36% of the mass measured with the AMS was organic mass. At 0.20, 0.15 and 0.10% supersaturation, closure could be achieved with different combinations of hygroscopic parameters and densities within the uncertainty range of the fit. The best agreement of the calculated CCN number concentration with the observed one was achieved when the organic fraction of the aerosol was treated as nearly water insoluble (κ org =0.02), leading to a mean total κ, κ tot , of 0.33 ± 0.13. However, several settings led to closure and κ org =0.2 is found to be an upper limit at 0.1% supersaturation. κ org ≤0.2 leads to a κ tot range of 0.33 ± 013 to 0.50 ± 0.11. Thus, the organic material ranges from being sparingly soluble to effectively insoluble. These results suggest that an increase in organic mass fraction in particles of a certain size would lead to a suppression of the Arctic CCN activity. Text Arctic oden Copernicus Publications: E-Journals Arctic Breaker ENVELOPE(-67.257,-67.257,-67.874,-67.874) Atmospheric Chemistry and Physics 11 22 11335 11350
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language English
description We present an aerosol – cloud condensation nuclei (CCN) closure study on summer high Arctic aerosol based on measurements that were carried out in 2008 during the Arctic Summer Cloud Ocean Study (ASCOS) on board the Swedish ice breaker Oden . The data presented here were collected during a three-week time period in the pack ice (>85° N) when the icebreaker Oden was moored to an ice floe and drifted passively during the most biological active period into autumn freeze up conditions. CCN number concentrations were obtained using two CCN counters measuring at different supersaturations. The directly measured CCN number concentration was then compared with a CCN number concentration calculated using both bulk aerosol mass composition data from an aerosol mass spectrometer (AMS) and aerosol number size distributions obtained from a differential mobility particle sizer, assuming κ-Köhler theory, surface tension of water and an internally mixed aerosol. The last assumption was supported by measurements made with a hygroscopic tandem differential mobility analyzer (HTDMA) for particles >70 nm. For the two highest measured supersaturations, 0.73 and 0.41%, closure could not be achieved with the investigated settings concerning hygroscopicity and density. The calculated CCN number concentration was always higher than the measured one for those two supersaturations. This might be caused by a relative larger insoluble organic mass fraction of the smaller particles that activate at these supersaturations, which are thus less good CCN than the larger particles. On average, 36% of the mass measured with the AMS was organic mass. At 0.20, 0.15 and 0.10% supersaturation, closure could be achieved with different combinations of hygroscopic parameters and densities within the uncertainty range of the fit. The best agreement of the calculated CCN number concentration with the observed one was achieved when the organic fraction of the aerosol was treated as nearly water insoluble (κ org =0.02), leading to a mean total κ, κ tot , of 0.33 ± 0.13. However, several settings led to closure and κ org =0.2 is found to be an upper limit at 0.1% supersaturation. κ org ≤0.2 leads to a κ tot range of 0.33 ± 013 to 0.50 ± 0.11. Thus, the organic material ranges from being sparingly soluble to effectively insoluble. These results suggest that an increase in organic mass fraction in particles of a certain size would lead to a suppression of the Arctic CCN activity.
format Text
author Martin, M.
Chang, R. Y.-W.
Sierau, B.
Sjogren, S.
Swietlicki, E.
Abbatt, J. P. D.
Leck, C.
Lohmann, U.
spellingShingle Martin, M.
Chang, R. Y.-W.
Sierau, B.
Sjogren, S.
Swietlicki, E.
Abbatt, J. P. D.
Leck, C.
Lohmann, U.
Cloud condensation nuclei closure study on summer arctic aerosol
author_facet Martin, M.
Chang, R. Y.-W.
Sierau, B.
Sjogren, S.
Swietlicki, E.
Abbatt, J. P. D.
Leck, C.
Lohmann, U.
author_sort Martin, M.
title Cloud condensation nuclei closure study on summer arctic aerosol
title_short Cloud condensation nuclei closure study on summer arctic aerosol
title_full Cloud condensation nuclei closure study on summer arctic aerosol
title_fullStr Cloud condensation nuclei closure study on summer arctic aerosol
title_full_unstemmed Cloud condensation nuclei closure study on summer arctic aerosol
title_sort cloud condensation nuclei closure study on summer arctic aerosol
publishDate 2018
url https://doi.org/10.5194/acp-11-11335-2011
https://www.atmos-chem-phys.net/11/11335/2011/
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op_source eISSN: 1680-7324
op_relation doi:10.5194/acp-11-11335-2011
https://www.atmos-chem-phys.net/11/11335/2011/
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container_title Atmospheric Chemistry and Physics
container_volume 11
container_issue 22
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