Please use this identifier to cite or link to this item: http://hdl.handle.net/2381/28288
Title: Seasonal observations of OH and HO[subscript 2] in the remote tropical marine boundary layer
Authors: Vaughan, S.
Ingham, T.
Whalley, L.K.
Stone, D.
Evans, M.J.
Read, K.A.
Lee, J.D.
Moller, S.J.
Carpenter, L.J.
Lewis, A.C
Fleming, Zoe L.
Heard, D.E.
First Published: 2012
Publisher: Copernicus GmbH (Copernicus Publications) on behalf of the European Geosciences Union (EGU).
Citation: Atmospheric Chemistry and Physics, 2012, 12 (4), 2149-2172
Abstract: Field measurements of the hydroxyl radical, OH, are crucial for our understanding of tropospheric chemistry. However, observations of this key atmospheric species in the tropical marine boundary layer, where the warm, humid conditions and high solar irradiance lend themselves favourably to production, are sparse. The Seasonal Oxidant Study at the Cape Verde Atmospheric Observatory in 2009 allowed, for the first time, seasonal measurements of both OH and HO[subscript 2] in a clean (i.e. low NO[subscript x]), tropical marine environment. It was found that concentrations of OH and HO[subscript 2] were typically higher in the summer months (June, September), with maximum daytime concentrations of ~9 × 10[superscript 6] and 4 × 10[superscript 8] molecule cm[superscript −3], respectively – almost double the values in winter (late February, early March). HO[subscript 2] was observed to persist at ~10[superscript 7] molecule cm[superscript −3] through the night, but there was no strong evidence of nighttime OH, consistent with previous measurements at the site in 2007. HO[subscript 2] was shown to have excellent correlations (R[superscript 2] ~ 0.90) with both the photolysis rate of ozone, J(O[superscript 1]D), and the primary production rate of OH, P(OH), from the reaction of O([superscript 1]D) with water vapour. The analogous relations of OH were not so strong (R[superscript 2] ~ 0.6), but the coefficients of the linear correlation with J(O[superscript 1]D) in this study were close to those yielded from previous works in this region, suggesting that the chemical regimes have similar impacts on the concentration of OH. Analysis of the variance of OH and HO[subscript 2] across the Seasonal Oxidant Study suggested that ~70% of the total variance could be explained by diurnal behaviour, with ~30% of the total variance being due to changes in air mass.
DOI Link: 10.5194/acp-12-2149-2012
ISSN: 1680-7316
eISSN: 1680-7324
Links: http://www.atmos-chem-phys.net/12/2149/2012/acp-12-2149-2012.html
http://hdl.handle.net/2381/28288
Version: Publisher Version
Status: Peer-reviewed
Type: Journal Article
Rights: © Author(s) 2012. This is an open-access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Appears in Collections:Published Articles, Dept. of Chemistry

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