The importance of Asia as a source of black carbon to the European Arctic during springtime 2013

Black carbon aerosol (BC) deposited to the Arctic sea ice or present in the free troposphere can significantly affect the Earth's radiation budget at high latitudes yet the BC burden in these regions and the regional source contributions are poorly constrained. Aircraft measurements of aerosol...

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Published in:Atmospheric Chemistry and Physics
Main Authors: D. Liu, B. Quennehen, E. Darbyshire, J. D. Allan, P. I. Williams, J. W. Taylor, S. J.-B. Bauguitte, M. J. Flynn, D. Lowe, M. W. Gallagher, K. N. Bower, T. W. Choularton, H. Coe
Format: Article in Journal/Newspaper
Language:English
Published: Copernicus Publications 2015
Subjects:
Online Access:https://doi.org/10.5194/acp-15-11537-2015
https://doaj.org/article/a68ab05b838f49a6a86309d8b59c3aed
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spelling ftdoajarticles:oai:doaj.org/article:a68ab05b838f49a6a86309d8b59c3aed 2023-05-15T14:48:43+02:00 The importance of Asia as a source of black carbon to the European Arctic during springtime 2013 D. Liu B. Quennehen E. Darbyshire J. D. Allan P. I. Williams J. W. Taylor S. J.-B. Bauguitte M. J. Flynn D. Lowe M. W. Gallagher K. N. Bower T. W. Choularton H. Coe 2015-10-01T00:00:00Z https://doi.org/10.5194/acp-15-11537-2015 https://doaj.org/article/a68ab05b838f49a6a86309d8b59c3aed EN eng Copernicus Publications http://www.atmos-chem-phys.net/15/11537/2015/acp-15-11537-2015.pdf https://doaj.org/toc/1680-7316 https://doaj.org/toc/1680-7324 1680-7316 1680-7324 doi:10.5194/acp-15-11537-2015 https://doaj.org/article/a68ab05b838f49a6a86309d8b59c3aed Atmospheric Chemistry and Physics, Vol 15, Iss 20, Pp 11537-11555 (2015) Physics QC1-999 Chemistry QD1-999 article 2015 ftdoajarticles https://doi.org/10.5194/acp-15-11537-2015 2022-12-30T22:40:36Z Black carbon aerosol (BC) deposited to the Arctic sea ice or present in the free troposphere can significantly affect the Earth's radiation budget at high latitudes yet the BC burden in these regions and the regional source contributions are poorly constrained. Aircraft measurements of aerosol composition in the European Arctic were conducted during the Aerosol–Cloud Coupling And Climate Interactions in the Arctic (ACCACIA) campaign in March 2013. Pollutant plumes were encountered throughout the lower to upper Arctic troposphere featuring enhancements in CO and aerosol mass loadings, which were chemically speciated into BC and non-refractory sulphate and organic matter. FLEXPART-WRF simulations have been performed to evaluate the likely contribution to the pollutants from regional ground sources. By combining up-to-date anthropogenic and open fire biomass burning (OBB) inventories, we have been able to compare the contributions made to the observed pollution layers from the sources of eastern/northern Asia (AS), Europe (EU) and North America (NA). Over 90 % of the contribution to the BC was shown to arise from non-OBB anthropogenic sources. AS sources were found to be the major contributor to the BC burden, increasing background BC loadings by a factor of 3–5 to 100.8 ± 48.4 ng sm −3 (in standard air m 3 at 273.15 K and 1013.25 mbar) and 55.8 ± 22.4 ng sm −3 in the middle and upper troposphere respectively. AS plumes close to the tropopause (about 7.5–8 km) were also observed, with BC concentrations ranging from 55 to 73 ng sm −3 , which will potentially have a significant radiative impact. EU sources influenced the middle troposphere with a BC mean concentration of 70.8 ± 39.1 ng sm −3 but made a minor contribution to the upper troposphere due to the relatively high latitude of the source region. The contribution of NA was shown to be much lower at all altitudes with BC mean concentration of 20 ng sm −3 . The BC transported to the Arctic is mixed with a non-BC volume fraction representing between 90–95 % of the ... Article in Journal/Newspaper Arctic black carbon Sea ice Directory of Open Access Journals: DOAJ Articles Arctic Atmospheric Chemistry and Physics 15 20 11537 11555
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
D. Liu
B. Quennehen
E. Darbyshire
J. D. Allan
P. I. Williams
J. W. Taylor
S. J.-B. Bauguitte
M. J. Flynn
D. Lowe
M. W. Gallagher
K. N. Bower
T. W. Choularton
H. Coe
The importance of Asia as a source of black carbon to the European Arctic during springtime 2013
topic_facet Physics
QC1-999
Chemistry
QD1-999
description Black carbon aerosol (BC) deposited to the Arctic sea ice or present in the free troposphere can significantly affect the Earth's radiation budget at high latitudes yet the BC burden in these regions and the regional source contributions are poorly constrained. Aircraft measurements of aerosol composition in the European Arctic were conducted during the Aerosol–Cloud Coupling And Climate Interactions in the Arctic (ACCACIA) campaign in March 2013. Pollutant plumes were encountered throughout the lower to upper Arctic troposphere featuring enhancements in CO and aerosol mass loadings, which were chemically speciated into BC and non-refractory sulphate and organic matter. FLEXPART-WRF simulations have been performed to evaluate the likely contribution to the pollutants from regional ground sources. By combining up-to-date anthropogenic and open fire biomass burning (OBB) inventories, we have been able to compare the contributions made to the observed pollution layers from the sources of eastern/northern Asia (AS), Europe (EU) and North America (NA). Over 90 % of the contribution to the BC was shown to arise from non-OBB anthropogenic sources. AS sources were found to be the major contributor to the BC burden, increasing background BC loadings by a factor of 3–5 to 100.8 ± 48.4 ng sm −3 (in standard air m 3 at 273.15 K and 1013.25 mbar) and 55.8 ± 22.4 ng sm −3 in the middle and upper troposphere respectively. AS plumes close to the tropopause (about 7.5–8 km) were also observed, with BC concentrations ranging from 55 to 73 ng sm −3 , which will potentially have a significant radiative impact. EU sources influenced the middle troposphere with a BC mean concentration of 70.8 ± 39.1 ng sm −3 but made a minor contribution to the upper troposphere due to the relatively high latitude of the source region. The contribution of NA was shown to be much lower at all altitudes with BC mean concentration of 20 ng sm −3 . The BC transported to the Arctic is mixed with a non-BC volume fraction representing between 90–95 % of the ...
format Article in Journal/Newspaper
author D. Liu
B. Quennehen
E. Darbyshire
J. D. Allan
P. I. Williams
J. W. Taylor
S. J.-B. Bauguitte
M. J. Flynn
D. Lowe
M. W. Gallagher
K. N. Bower
T. W. Choularton
H. Coe
author_facet D. Liu
B. Quennehen
E. Darbyshire
J. D. Allan
P. I. Williams
J. W. Taylor
S. J.-B. Bauguitte
M. J. Flynn
D. Lowe
M. W. Gallagher
K. N. Bower
T. W. Choularton
H. Coe
author_sort D. Liu
title The importance of Asia as a source of black carbon to the European Arctic during springtime 2013
title_short The importance of Asia as a source of black carbon to the European Arctic during springtime 2013
title_full The importance of Asia as a source of black carbon to the European Arctic during springtime 2013
title_fullStr The importance of Asia as a source of black carbon to the European Arctic during springtime 2013
title_full_unstemmed The importance of Asia as a source of black carbon to the European Arctic during springtime 2013
title_sort importance of asia as a source of black carbon to the european arctic during springtime 2013
publisher Copernicus Publications
publishDate 2015
url https://doi.org/10.5194/acp-15-11537-2015
https://doaj.org/article/a68ab05b838f49a6a86309d8b59c3aed
geographic Arctic
geographic_facet Arctic
genre Arctic
black carbon
Sea ice
genre_facet Arctic
black carbon
Sea ice
op_source Atmospheric Chemistry and Physics, Vol 15, Iss 20, Pp 11537-11555 (2015)
op_relation http://www.atmos-chem-phys.net/15/11537/2015/acp-15-11537-2015.pdf
https://doaj.org/toc/1680-7316
https://doaj.org/toc/1680-7324
1680-7316
1680-7324
doi:10.5194/acp-15-11537-2015
https://doaj.org/article/a68ab05b838f49a6a86309d8b59c3aed
op_doi https://doi.org/10.5194/acp-15-11537-2015
container_title Atmospheric Chemistry and Physics
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container_issue 20
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