Observations of OH and HO2 radicals in coastal Antarctica

OH and HO<sub>2</sub> radical concentrations have been measured in the boundary layer of coastal Antarctica for a six-week period during the austral summer of 2005. The measurements were performed at the British Antarctic Survey's Halley Research Station (75&deg; 35' S, 26&...

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Main Authors: S. J.-B. Bauguitte, H. K. Roscoe, D. E. Heard, R. A. Salmon, J. D. Lee, W. J. Bloss, A. E. Jones
Format: Article
Language:English
Published: Copernicus Publications 2007-08-01
Series:Atmospheric Chemistry and Physics
Online Access:http://www.atmos-chem-phys.net/7/4171/2007/acp-7-4171-2007.pdf
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spelling doaj-283beb54234340a28b918dfde38358682020-11-25T00:09:42ZengCopernicus PublicationsAtmospheric Chemistry and Physics1680-73161680-73242007-08-0171641714185Observations of OH and HO2 radicals in coastal AntarcticaS. J.-B. BauguitteH. K. RoscoeD. E. HeardR. A. SalmonJ. D. LeeW. J. BlossA. E. JonesOH and HO<sub>2</sub> radical concentrations have been measured in the boundary layer of coastal Antarctica for a six-week period during the austral summer of 2005. The measurements were performed at the British Antarctic Survey's Halley Research Station (75&deg; 35' S, 26&deg; 19' W), using the technique of on-resonance laser-induced fluorescence to detect OH, with HO<sub>2</sub> measured following chemical conversion through addition of NO. The mean radical levels were 3.9&times;10<sup>5</sup> molecule cm<sup>&minus;3</sup> for OH, and 0.76 ppt for HO<sub>2</sub> (ppt denotes parts per trillion, by volume). Typical maximum (local noontime) levels were 7.9&times;10<sup>5</sup> molecule cm<sup>&minus;3</sup> and 1.50 ppt for OH and HO<sub>2</sub> respectively. The main sources of HO<sub>x</sub> were photolysis of O<sub>3</sub> and HCHO, with potentially important but uncertain contributions from HONO and higher aldehydes. Of the measured OH sinks, reaction with CO and CH<sub>4</sub> dominated, however comparison of the observed OH concentrations with those calculated via the steady state approximation indicated that additional co-reactants were likely to have been present. Elevated levels of NO<sub>x</sub> resulting from snowpack photochemistry contributed to HO<sub>x</sub> cycling and enhanced levels of OH, however the halogen oxides IO and BrO dominated the CH<sub>3</sub>O<sub>2</sub> &ndash; HO<sub>2</sub> &ndash; OH conversion in this environment, with associated ozone destruction. http://www.atmos-chem-phys.net/7/4171/2007/acp-7-4171-2007.pdf
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language English
format Article
sources DOAJ
author S. J.-B. Bauguitte
H. K. Roscoe
D. E. Heard
R. A. Salmon
J. D. Lee
W. J. Bloss
A. E. Jones
spellingShingle S. J.-B. Bauguitte
H. K. Roscoe
D. E. Heard
R. A. Salmon
J. D. Lee
W. J. Bloss
A. E. Jones
Observations of OH and HO2 radicals in coastal Antarctica
Atmospheric Chemistry and Physics
author_facet S. J.-B. Bauguitte
H. K. Roscoe
D. E. Heard
R. A. Salmon
J. D. Lee
W. J. Bloss
A. E. Jones
author_sort S. J.-B. Bauguitte
title Observations of OH and HO2 radicals in coastal Antarctica
title_short Observations of OH and HO2 radicals in coastal Antarctica
title_full Observations of OH and HO2 radicals in coastal Antarctica
title_fullStr Observations of OH and HO2 radicals in coastal Antarctica
title_full_unstemmed Observations of OH and HO2 radicals in coastal Antarctica
title_sort observations of oh and ho2 radicals in coastal antarctica
publisher Copernicus Publications
series Atmospheric Chemistry and Physics
issn 1680-7316
1680-7324
publishDate 2007-08-01
description OH and HO<sub>2</sub> radical concentrations have been measured in the boundary layer of coastal Antarctica for a six-week period during the austral summer of 2005. The measurements were performed at the British Antarctic Survey's Halley Research Station (75&deg; 35' S, 26&deg; 19' W), using the technique of on-resonance laser-induced fluorescence to detect OH, with HO<sub>2</sub> measured following chemical conversion through addition of NO. The mean radical levels were 3.9&times;10<sup>5</sup> molecule cm<sup>&minus;3</sup> for OH, and 0.76 ppt for HO<sub>2</sub> (ppt denotes parts per trillion, by volume). Typical maximum (local noontime) levels were 7.9&times;10<sup>5</sup> molecule cm<sup>&minus;3</sup> and 1.50 ppt for OH and HO<sub>2</sub> respectively. The main sources of HO<sub>x</sub> were photolysis of O<sub>3</sub> and HCHO, with potentially important but uncertain contributions from HONO and higher aldehydes. Of the measured OH sinks, reaction with CO and CH<sub>4</sub> dominated, however comparison of the observed OH concentrations with those calculated via the steady state approximation indicated that additional co-reactants were likely to have been present. Elevated levels of NO<sub>x</sub> resulting from snowpack photochemistry contributed to HO<sub>x</sub> cycling and enhanced levels of OH, however the halogen oxides IO and BrO dominated the CH<sub>3</sub>O<sub>2</sub> &ndash; HO<sub>2</sub> &ndash; OH conversion in this environment, with associated ozone destruction.
url http://www.atmos-chem-phys.net/7/4171/2007/acp-7-4171-2007.pdf
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