Longpath DOAS observations of surface BrO at Summit, Greenland

Reactive halogens, and in particular bromine oxide (BrO), have frequently been observed in regions with large halide reservoirs, for example during bromine catalyzed coastal polar ozone depletion events. Much less is known about the presence and impact of reactive halogens in areas without obvious h...

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Main Authors: J. Stutz, J. L. Thomas, S. C. Hurlock, M. Schneider, R. von Glasow, M. Piot, K. Gorham, J. F. Burkhart, L. Ziemba, J. E. Dibb, B. L. Lefer
Format: Article
Language:English
Published: Copernicus Publications 2011-09-01
Series:Atmospheric Chemistry and Physics
Online Access:http://www.atmos-chem-phys.net/11/9899/2011/acp-11-9899-2011.pdf
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spelling doaj-6af5e7855ead41a4895a957beb60b5d82020-11-25T00:48:26ZengCopernicus PublicationsAtmospheric Chemistry and Physics1680-73161680-73242011-09-0111189899991010.5194/acp-11-9899-2011Longpath DOAS observations of surface BrO at Summit, GreenlandJ. StutzJ. L. ThomasS. C. HurlockM. SchneiderR. von GlasowM. PiotK. GorhamJ. F. BurkhartL. ZiembaJ. E. DibbB. L. LeferReactive halogens, and in particular bromine oxide (BrO), have frequently been observed in regions with large halide reservoirs, for example during bromine catalyzed coastal polar ozone depletion events. Much less is known about the presence and impact of reactive halogens in areas without obvious halide reservoirs, such as the polar ice sheets or continental snow. <br><br> We report the first LP-DOAS measurements of BrO at Summit research station in the center of the Greenland ice sheet at an altitude of 3200 m. BrO mixing ratios in May 2007 and June 2008 were typically between 1–3 pmol mol<sup>−1</sup>, with maxima of up to 5 pmol mol<sup>−1</sup>. These measurements unequivocally show that halogen chemistry is occurring in the remote Arctic, far from known bromine reservoirs, such as the ocean. During periods when FLEXPART retroplumes show that airmasses resided on the Greenland ice sheet for 3 or more days, BrO exhibits a clear diurnal variation, with peak mixing ratios of up to 3 pmol mol<sup>−1</sup> in the morning and at night. The diurnal cycle of BrO can be explained by a changing boundary layer height combined with photochemical formation of reactive bromine driven by solar radiation at the snow surface. The shallow stable boundary layer in the morning and night leads to an accumulation of BrO at the surface, leading to elevated BrO despite the expected smaller release from the snowpack during these times of low solar radiation. During the day when photolytic formation of reactive bromine is expected to be highest, efficient mixing into a deeper neutral boundary layer leads to lower BrO mixing ratios than during mornings and nights. <br><br> The extended period of contact with the Greenland snowpack combined with the diurnal profile of BrO, modulated by boundary layer height, suggests that photochemistry in the snow is a significant source of BrO measured at Summit during the 2008 experiment. In addition, a rapid transport event on 4 July 2008, during which marine air from the Greenland east coast was rapidly transported to Summit, led to enhanced mixing ratios of BrO and a number of marine tracers. However, rapid transport of marine air from the Greenland east coast is rare and most likely not the main source of bromide in surface snow at Summit. The observed levels of BrO are predicted to influence NO<sub>x</sub> chemistry as well as impact HO<sub>x</sub> partitioning. However, impact of local snow photochemistry on HO<sub>x</sub> is smaller than previously suggested for Summit.http://www.atmos-chem-phys.net/11/9899/2011/acp-11-9899-2011.pdf
collection DOAJ
language English
format Article
sources DOAJ
author J. Stutz
J. L. Thomas
S. C. Hurlock
M. Schneider
R. von Glasow
M. Piot
K. Gorham
J. F. Burkhart
L. Ziemba
J. E. Dibb
B. L. Lefer
spellingShingle J. Stutz
J. L. Thomas
S. C. Hurlock
M. Schneider
R. von Glasow
M. Piot
K. Gorham
J. F. Burkhart
L. Ziemba
J. E. Dibb
B. L. Lefer
Longpath DOAS observations of surface BrO at Summit, Greenland
Atmospheric Chemistry and Physics
author_facet J. Stutz
J. L. Thomas
S. C. Hurlock
M. Schneider
R. von Glasow
M. Piot
K. Gorham
J. F. Burkhart
L. Ziemba
J. E. Dibb
B. L. Lefer
author_sort J. Stutz
title Longpath DOAS observations of surface BrO at Summit, Greenland
title_short Longpath DOAS observations of surface BrO at Summit, Greenland
title_full Longpath DOAS observations of surface BrO at Summit, Greenland
title_fullStr Longpath DOAS observations of surface BrO at Summit, Greenland
title_full_unstemmed Longpath DOAS observations of surface BrO at Summit, Greenland
title_sort longpath doas observations of surface bro at summit, greenland
publisher Copernicus Publications
series Atmospheric Chemistry and Physics
issn 1680-7316
1680-7324
publishDate 2011-09-01
description Reactive halogens, and in particular bromine oxide (BrO), have frequently been observed in regions with large halide reservoirs, for example during bromine catalyzed coastal polar ozone depletion events. Much less is known about the presence and impact of reactive halogens in areas without obvious halide reservoirs, such as the polar ice sheets or continental snow. <br><br> We report the first LP-DOAS measurements of BrO at Summit research station in the center of the Greenland ice sheet at an altitude of 3200 m. BrO mixing ratios in May 2007 and June 2008 were typically between 1–3 pmol mol<sup>−1</sup>, with maxima of up to 5 pmol mol<sup>−1</sup>. These measurements unequivocally show that halogen chemistry is occurring in the remote Arctic, far from known bromine reservoirs, such as the ocean. During periods when FLEXPART retroplumes show that airmasses resided on the Greenland ice sheet for 3 or more days, BrO exhibits a clear diurnal variation, with peak mixing ratios of up to 3 pmol mol<sup>−1</sup> in the morning and at night. The diurnal cycle of BrO can be explained by a changing boundary layer height combined with photochemical formation of reactive bromine driven by solar radiation at the snow surface. The shallow stable boundary layer in the morning and night leads to an accumulation of BrO at the surface, leading to elevated BrO despite the expected smaller release from the snowpack during these times of low solar radiation. During the day when photolytic formation of reactive bromine is expected to be highest, efficient mixing into a deeper neutral boundary layer leads to lower BrO mixing ratios than during mornings and nights. <br><br> The extended period of contact with the Greenland snowpack combined with the diurnal profile of BrO, modulated by boundary layer height, suggests that photochemistry in the snow is a significant source of BrO measured at Summit during the 2008 experiment. In addition, a rapid transport event on 4 July 2008, during which marine air from the Greenland east coast was rapidly transported to Summit, led to enhanced mixing ratios of BrO and a number of marine tracers. However, rapid transport of marine air from the Greenland east coast is rare and most likely not the main source of bromide in surface snow at Summit. The observed levels of BrO are predicted to influence NO<sub>x</sub> chemistry as well as impact HO<sub>x</sub> partitioning. However, impact of local snow photochemistry on HO<sub>x</sub> is smaller than previously suggested for Summit.
url http://www.atmos-chem-phys.net/11/9899/2011/acp-11-9899-2011.pdf
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