On the potential contribution of open lead particle emissions to the central Arctic aerosol concentration

We present direct eddy covariance measurements of aerosol number fluxes, dominated by sub-50 nm particles, at the edge of an ice floe drifting in the central Arctic Ocean. The measurements were made during the ice-breaker borne ASCOS (Arctic Summer Cloud Ocean Study) expedition in August 2008 betwee...

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Published in:Atmospheric Chemistry and Physics
Main Authors: A. Held, I. M. Brooks, C. Leck, M. Tjernström
Format: Article in Journal/Newspaper
Language:English
Published: Copernicus Publications 2011
Subjects:
Online Access:https://doi.org/10.5194/acp-11-3093-2011
https://doaj.org/article/b7142ef235a24db1af7dce1ad66d9652
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spelling ftdoajarticles:oai:doaj.org/article:b7142ef235a24db1af7dce1ad66d9652 2023-05-15T14:51:40+02:00 On the potential contribution of open lead particle emissions to the central Arctic aerosol concentration A. Held I. M. Brooks C. Leck M. Tjernström 2011-04-01T00:00:00Z https://doi.org/10.5194/acp-11-3093-2011 https://doaj.org/article/b7142ef235a24db1af7dce1ad66d9652 EN eng Copernicus Publications http://www.atmos-chem-phys.net/11/3093/2011/acp-11-3093-2011.pdf https://doaj.org/toc/1680-7316 https://doaj.org/toc/1680-7324 doi:10.5194/acp-11-3093-2011 1680-7316 1680-7324 https://doaj.org/article/b7142ef235a24db1af7dce1ad66d9652 Atmospheric Chemistry and Physics, Vol 11, Iss 7, Pp 3093-3105 (2011) Physics QC1-999 Chemistry QD1-999 article 2011 ftdoajarticles https://doi.org/10.5194/acp-11-3093-2011 2022-12-31T11:20:24Z We present direct eddy covariance measurements of aerosol number fluxes, dominated by sub-50 nm particles, at the edge of an ice floe drifting in the central Arctic Ocean. The measurements were made during the ice-breaker borne ASCOS (Arctic Summer Cloud Ocean Study) expedition in August 2008 between 2°–10° W longitude and 87°–87.5° N latitude. The median aerosol transfer velocities over different surface types (open water leads, ice ridges, snow and ice surfaces) ranged from 0.27 to 0.68 mm s −1 during deposition-dominated episodes. Emission periods were observed more frequently over the open lead, while the snow behaved primarily as a deposition surface. Directly measured aerosol fluxes were compared with particle deposition parameterizations in order to estimate the emission flux from the observed net aerosol flux. Finally, the contribution of the open lead particle source to atmospheric variations in particle number concentration was evaluated and compared with the observed temporal evolution of particle number. The direct emission of aerosol particles from the open lead can explain only 5–10% of the observed particle number variation in the mixing layer close to the surface. Article in Journal/Newspaper Arctic Arctic Ocean Directory of Open Access Journals: DOAJ Articles Arctic Arctic Ocean Breaker ENVELOPE(-67.257,-67.257,-67.874,-67.874) Atmospheric Chemistry and Physics 11 7 3093 3105
institution Open Polar
collection Directory of Open Access Journals: DOAJ Articles
op_collection_id ftdoajarticles
language English
topic Physics
QC1-999
Chemistry
QD1-999
spellingShingle Physics
QC1-999
Chemistry
QD1-999
A. Held
I. M. Brooks
C. Leck
M. Tjernström
On the potential contribution of open lead particle emissions to the central Arctic aerosol concentration
topic_facet Physics
QC1-999
Chemistry
QD1-999
description We present direct eddy covariance measurements of aerosol number fluxes, dominated by sub-50 nm particles, at the edge of an ice floe drifting in the central Arctic Ocean. The measurements were made during the ice-breaker borne ASCOS (Arctic Summer Cloud Ocean Study) expedition in August 2008 between 2°–10° W longitude and 87°–87.5° N latitude. The median aerosol transfer velocities over different surface types (open water leads, ice ridges, snow and ice surfaces) ranged from 0.27 to 0.68 mm s −1 during deposition-dominated episodes. Emission periods were observed more frequently over the open lead, while the snow behaved primarily as a deposition surface. Directly measured aerosol fluxes were compared with particle deposition parameterizations in order to estimate the emission flux from the observed net aerosol flux. Finally, the contribution of the open lead particle source to atmospheric variations in particle number concentration was evaluated and compared with the observed temporal evolution of particle number. The direct emission of aerosol particles from the open lead can explain only 5–10% of the observed particle number variation in the mixing layer close to the surface.
format Article in Journal/Newspaper
author A. Held
I. M. Brooks
C. Leck
M. Tjernström
author_facet A. Held
I. M. Brooks
C. Leck
M. Tjernström
author_sort A. Held
title On the potential contribution of open lead particle emissions to the central Arctic aerosol concentration
title_short On the potential contribution of open lead particle emissions to the central Arctic aerosol concentration
title_full On the potential contribution of open lead particle emissions to the central Arctic aerosol concentration
title_fullStr On the potential contribution of open lead particle emissions to the central Arctic aerosol concentration
title_full_unstemmed On the potential contribution of open lead particle emissions to the central Arctic aerosol concentration
title_sort on the potential contribution of open lead particle emissions to the central arctic aerosol concentration
publisher Copernicus Publications
publishDate 2011
url https://doi.org/10.5194/acp-11-3093-2011
https://doaj.org/article/b7142ef235a24db1af7dce1ad66d9652
long_lat ENVELOPE(-67.257,-67.257,-67.874,-67.874)
geographic Arctic
Arctic Ocean
Breaker
geographic_facet Arctic
Arctic Ocean
Breaker
genre Arctic
Arctic Ocean
genre_facet Arctic
Arctic Ocean
op_source Atmospheric Chemistry and Physics, Vol 11, Iss 7, Pp 3093-3105 (2011)
op_relation http://www.atmos-chem-phys.net/11/3093/2011/acp-11-3093-2011.pdf
https://doaj.org/toc/1680-7316
https://doaj.org/toc/1680-7324
doi:10.5194/acp-11-3093-2011
1680-7316
1680-7324
https://doaj.org/article/b7142ef235a24db1af7dce1ad66d9652
op_doi https://doi.org/10.5194/acp-11-3093-2011
container_title Atmospheric Chemistry and Physics
container_volume 11
container_issue 7
container_start_page 3093
op_container_end_page 3105
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