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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Bibliographic Details
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
Description
Summary: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.
ISSN:1680-7316
1680-7324