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: Held, A, Brooks, IM, Leck, C, Tjernstrom, M
Format: Article in Journal/Newspaper
Language:English
Published: European Geosciences Union 2011
Subjects:
Online Access:https://eprints.whiterose.ac.uk/77221/
https://eprints.whiterose.ac.uk/77221/7/Held_2011_acp-11-3093-2011_with_coversheet.pdf
https://doi.org/10.5194/acp-11-3093-2011
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spelling ftleedsuniv:oai:eprints.whiterose.ac.uk:77221 2024-06-02T07:59:43+00:00 On the potential contribution of open lead particle emissions to the central Arctic aerosol concentration Held, A Brooks, IM Leck, C Tjernstrom, M 2011 text https://eprints.whiterose.ac.uk/77221/ https://eprints.whiterose.ac.uk/77221/7/Held_2011_acp-11-3093-2011_with_coversheet.pdf https://doi.org/10.5194/acp-11-3093-2011 en eng European Geosciences Union https://eprints.whiterose.ac.uk/77221/7/Held_2011_acp-11-3093-2011_with_coversheet.pdf Held, A, Brooks, IM, Leck, C et al. (1 more author) (2011) On the potential contribution of open lead particle emissions to the central Arctic aerosol concentration. Atmospheric Chemistry and Physics, 11 (7). 3093 - 3105. ISSN 1680-7316 Article NonPeerReviewed 2011 ftleedsuniv https://doi.org/10.5194/acp-11-3093-2011 2024-05-06T12:40:54Z 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 5ĝ€"10% of the observed particle number variation in the mixing layer close to the surface. Article in Journal/Newspaper Arctic Arctic Arctic Ocean White Rose Research Online (Universities of Leeds, Sheffield & York) 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 White Rose Research Online (Universities of Leeds, Sheffield & York)
op_collection_id ftleedsuniv
language English
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 5ĝ€"10% of the observed particle number variation in the mixing layer close to the surface.
format Article in Journal/Newspaper
author Held, A
Brooks, IM
Leck, C
Tjernstrom, M
spellingShingle Held, A
Brooks, IM
Leck, C
Tjernstrom, M
On the potential contribution of open lead particle emissions to the central Arctic aerosol concentration
author_facet Held, A
Brooks, IM
Leck, C
Tjernstrom, M
author_sort Held, A
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 European Geosciences Union
publishDate 2011
url https://eprints.whiterose.ac.uk/77221/
https://eprints.whiterose.ac.uk/77221/7/Held_2011_acp-11-3093-2011_with_coversheet.pdf
https://doi.org/10.5194/acp-11-3093-2011
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
Arctic Ocean
genre_facet Arctic
Arctic
Arctic Ocean
op_relation https://eprints.whiterose.ac.uk/77221/7/Held_2011_acp-11-3093-2011_with_coversheet.pdf
Held, A, Brooks, IM, Leck, C et al. (1 more author) (2011) On the potential contribution of open lead particle emissions to the central Arctic aerosol concentration. Atmospheric Chemistry and Physics, 11 (7). 3093 - 3105. ISSN 1680-7316
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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