Wildfire smoke in the Siberian Arctic in summer: source characterization and plume evolution from airborne measurements

We present airborne measurements of carbon dioxide (CO<sub>2</sub>), carbon monoxide (CO), ozone (O<sub>3</sub>), equivalent black carbon (EBC) and ultra fine particles over North-Eastern Siberia in July 2008 performed during the YAK-AEROSIB/PO...

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Main Authors: P. Ciais, B. D. Belan, V. P. Shmargunov, K. S. Law, M. V. Panchenko, P. Nédélec, M. Yu. Arshinov, A. Stohl, J.-D. Paris
Format: Article
Language:English
Published: Copernicus Publications 2009-12-01
Series:Atmospheric Chemistry and Physics
Online Access:http://www.atmos-chem-phys.net/9/9315/2009/acp-9-9315-2009.pdf
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spelling doaj-4132d6e1865746aeb3f51f5c9033cbe62020-11-24T22:02:00ZengCopernicus PublicationsAtmospheric Chemistry and Physics1680-73161680-73242009-12-0192393159327Wildfire smoke in the Siberian Arctic in summer: source characterization and plume evolution from airborne measurementsP. CiaisB. D. BelanV. P. ShmargunovK. S. LawM. V. PanchenkoP. NédélecM. Yu. ArshinovA. StohlJ.-D. ParisWe present airborne measurements of carbon dioxide (CO<sub>2</sub>), carbon monoxide (CO), ozone (O<sub>3</sub>), equivalent black carbon (EBC) and ultra fine particles over North-Eastern Siberia in July 2008 performed during the YAK-AEROSIB/POLARCAT experiment. During a "golden day" (11 July 2008) a number of biomass burning plumes were encountered with CO mixing ratio enhancements of up to 500 ppb relative to a background of 90 ppb. Number concentrations of aerosols in the size range 3.5–200 nm peaked at 4000 cm<sup>−3</sup> and the EBC content reached 1.4 μg m<sup>−3</sup>. These high concentrations were caused by forest fires in the vicinity of the landing airport in Yakutsk where measurements in fresh smoke could be made during the descent. We estimate a combustion efficiency of 90 ± 3% based on CO and CO<sub>2</sub> measurements and a CO emission factor of 65.5 ± 10.8 g CO per kilogram of dry matter burned. This suggests a potential increase in the average northern hemispheric CO mixing ratio of 3.0–7.2 ppb per million hectares of Siberian forest burned. For BC, we estimate an emission factor of 0.52 ± 0.07 g BC kg<sup>−1</sup>, comparable to values reported in the literature. The emission ratio of ultra-fine particles (3.5–200 nm) was 26 cm<sup>−3</sup> (ppb CO)<sup>−1</sup>, consistent with other airborne studies. <br><br> The transport of identified biomass burning plumes was investigated using the FLEXPART Lagrangian model. Based on sampling of wildfire plumes from the same source but with different atmospheric ages derived from FLEXPART, we estimate that the e-folding lifetimes of EBC and ultra fine particles (between 3.5 and 200 nm in size) against removal and growth processes are 5.1 and 5.5 days respectively, supporting lifetime estimates used in various modelling studies. http://www.atmos-chem-phys.net/9/9315/2009/acp-9-9315-2009.pdf
collection DOAJ
language English
format Article
sources DOAJ
author P. Ciais
B. D. Belan
V. P. Shmargunov
K. S. Law
M. V. Panchenko
P. Nédélec
M. Yu. Arshinov
A. Stohl
J.-D. Paris
spellingShingle P. Ciais
B. D. Belan
V. P. Shmargunov
K. S. Law
M. V. Panchenko
P. Nédélec
M. Yu. Arshinov
A. Stohl
J.-D. Paris
Wildfire smoke in the Siberian Arctic in summer: source characterization and plume evolution from airborne measurements
Atmospheric Chemistry and Physics
author_facet P. Ciais
B. D. Belan
V. P. Shmargunov
K. S. Law
M. V. Panchenko
P. Nédélec
M. Yu. Arshinov
A. Stohl
J.-D. Paris
author_sort P. Ciais
title Wildfire smoke in the Siberian Arctic in summer: source characterization and plume evolution from airborne measurements
title_short Wildfire smoke in the Siberian Arctic in summer: source characterization and plume evolution from airborne measurements
title_full Wildfire smoke in the Siberian Arctic in summer: source characterization and plume evolution from airborne measurements
title_fullStr Wildfire smoke in the Siberian Arctic in summer: source characterization and plume evolution from airborne measurements
title_full_unstemmed Wildfire smoke in the Siberian Arctic in summer: source characterization and plume evolution from airborne measurements
title_sort wildfire smoke in the siberian arctic in summer: source characterization and plume evolution from airborne measurements
publisher Copernicus Publications
series Atmospheric Chemistry and Physics
issn 1680-7316
1680-7324
publishDate 2009-12-01
description We present airborne measurements of carbon dioxide (CO<sub>2</sub>), carbon monoxide (CO), ozone (O<sub>3</sub>), equivalent black carbon (EBC) and ultra fine particles over North-Eastern Siberia in July 2008 performed during the YAK-AEROSIB/POLARCAT experiment. During a "golden day" (11 July 2008) a number of biomass burning plumes were encountered with CO mixing ratio enhancements of up to 500 ppb relative to a background of 90 ppb. Number concentrations of aerosols in the size range 3.5–200 nm peaked at 4000 cm<sup>−3</sup> and the EBC content reached 1.4 μg m<sup>−3</sup>. These high concentrations were caused by forest fires in the vicinity of the landing airport in Yakutsk where measurements in fresh smoke could be made during the descent. We estimate a combustion efficiency of 90 ± 3% based on CO and CO<sub>2</sub> measurements and a CO emission factor of 65.5 ± 10.8 g CO per kilogram of dry matter burned. This suggests a potential increase in the average northern hemispheric CO mixing ratio of 3.0–7.2 ppb per million hectares of Siberian forest burned. For BC, we estimate an emission factor of 0.52 ± 0.07 g BC kg<sup>−1</sup>, comparable to values reported in the literature. The emission ratio of ultra-fine particles (3.5–200 nm) was 26 cm<sup>−3</sup> (ppb CO)<sup>−1</sup>, consistent with other airborne studies. <br><br> The transport of identified biomass burning plumes was investigated using the FLEXPART Lagrangian model. Based on sampling of wildfire plumes from the same source but with different atmospheric ages derived from FLEXPART, we estimate that the e-folding lifetimes of EBC and ultra fine particles (between 3.5 and 200 nm in size) against removal and growth processes are 5.1 and 5.5 days respectively, supporting lifetime estimates used in various modelling studies.
url http://www.atmos-chem-phys.net/9/9315/2009/acp-9-9315-2009.pdf
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