Measurement and modelling of tropospheric reactive halogen species over the tropical Atlantic Ocean

Although tropospheric reactive halogen chemistry is well studied in coastal and polar environments, the presence of halogens over the open ocean environment has not been widely reported. The impacts of halogens on the tropical open ocean marine boundary layer (MBL), in particular, are not well chara...

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Main Authors: A. S. Mahajan, J. M. C. Plane, H. Oetjen, L. Mendes, R. W. Saunders, A. Saiz-Lopez, C. E. Jones, L. J. Carpenter, G. B. McFiggans
Format: Article
Language:English
Published: Copernicus Publications 2010-05-01
Series:Atmospheric Chemistry and Physics
Online Access:http://www.atmos-chem-phys.net/10/4611/2010/acp-10-4611-2010.pdf
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spelling doaj-f898bae87637482d91a9d13bd55eef2b2020-11-24T23:41:47ZengCopernicus PublicationsAtmospheric Chemistry and Physics1680-73161680-73242010-05-0110104611462410.5194/acp-10-4611-2010Measurement and modelling of tropospheric reactive halogen species over the tropical Atlantic OceanA. S. MahajanJ. M. C. PlaneH. OetjenL. MendesR. W. SaundersA. Saiz-LopezC. E. JonesL. J. CarpenterG. B. McFiggansAlthough tropospheric reactive halogen chemistry is well studied in coastal and polar environments, the presence of halogens over the open ocean environment has not been widely reported. The impacts of halogens on the tropical open ocean marine boundary layer (MBL), in particular, are not well characterised. This paper describes observations of iodine monoxide (IO) and bromine oxide (BrO) over eight months in the tropical open ocean MBL, on the north-eastern side of São Vicente (Cape Verde Islands, 16.85° N, 24.87° W). The highest BrO mixing ratio observed was 5.6±1 pmol mol<sup>−1</sup>, while the maximum observed IO mixing ratio was 3.1±0.4 pmol mol<sup>−1</sup>. The average values seen between 09:00–17:00 GMT were ~2.8 pmol mol<sup>−1</sup> for BrO and ~1.5 pmol mol<sup>−1</sup> for IO; these averages showed little variability over the entire campaign from November 2006 to June 2007. A 1-dimensional chemistry and transport model is used to study the evolution of iodine species and quantify the combined impact of iodine and bromine chemistry on the oxidising capacity of the MBL. It appears that the measured fluxes of iodocarbons are insufficient to account for the observed levels of IO, and that an additional I atom source is required, possibly caused by the deposition of O<sub>3</sub> onto the ocean surface in the presence of solar radiation. Modelling results also show that the O<sub>3</sub> depletion observed at Cape Verde cannot be explained in the absence of halogen chemistry, which contributes ~45% of the observed O<sub>3</sub> depletion at the height of measurements (10 m) during summer. The model also predicts that halogens decrease the hydroperoxy radical (HO<sub>2</sub>) concentration by ~14% and increase the hydroxyl radical (OH) concentration by ~13% near the ocean surface. The oxidation of dimethyl sulphide (DMS) by BrO takes place at a comparable rate to oxidation by OH in this environment. Finally, the potential of iodine chemistry to form new particles is explored and conditions under which particle formation could be important in the remote MBL are discussed. http://www.atmos-chem-phys.net/10/4611/2010/acp-10-4611-2010.pdf
collection DOAJ
language English
format Article
sources DOAJ
author A. S. Mahajan
J. M. C. Plane
H. Oetjen
L. Mendes
R. W. Saunders
A. Saiz-Lopez
C. E. Jones
L. J. Carpenter
G. B. McFiggans
spellingShingle A. S. Mahajan
J. M. C. Plane
H. Oetjen
L. Mendes
R. W. Saunders
A. Saiz-Lopez
C. E. Jones
L. J. Carpenter
G. B. McFiggans
Measurement and modelling of tropospheric reactive halogen species over the tropical Atlantic Ocean
Atmospheric Chemistry and Physics
author_facet A. S. Mahajan
J. M. C. Plane
H. Oetjen
L. Mendes
R. W. Saunders
A. Saiz-Lopez
C. E. Jones
L. J. Carpenter
G. B. McFiggans
author_sort A. S. Mahajan
title Measurement and modelling of tropospheric reactive halogen species over the tropical Atlantic Ocean
title_short Measurement and modelling of tropospheric reactive halogen species over the tropical Atlantic Ocean
title_full Measurement and modelling of tropospheric reactive halogen species over the tropical Atlantic Ocean
title_fullStr Measurement and modelling of tropospheric reactive halogen species over the tropical Atlantic Ocean
title_full_unstemmed Measurement and modelling of tropospheric reactive halogen species over the tropical Atlantic Ocean
title_sort measurement and modelling of tropospheric reactive halogen species over the tropical atlantic ocean
publisher Copernicus Publications
series Atmospheric Chemistry and Physics
issn 1680-7316
1680-7324
publishDate 2010-05-01
description Although tropospheric reactive halogen chemistry is well studied in coastal and polar environments, the presence of halogens over the open ocean environment has not been widely reported. The impacts of halogens on the tropical open ocean marine boundary layer (MBL), in particular, are not well characterised. This paper describes observations of iodine monoxide (IO) and bromine oxide (BrO) over eight months in the tropical open ocean MBL, on the north-eastern side of São Vicente (Cape Verde Islands, 16.85° N, 24.87° W). The highest BrO mixing ratio observed was 5.6±1 pmol mol<sup>−1</sup>, while the maximum observed IO mixing ratio was 3.1±0.4 pmol mol<sup>−1</sup>. The average values seen between 09:00–17:00 GMT were ~2.8 pmol mol<sup>−1</sup> for BrO and ~1.5 pmol mol<sup>−1</sup> for IO; these averages showed little variability over the entire campaign from November 2006 to June 2007. A 1-dimensional chemistry and transport model is used to study the evolution of iodine species and quantify the combined impact of iodine and bromine chemistry on the oxidising capacity of the MBL. It appears that the measured fluxes of iodocarbons are insufficient to account for the observed levels of IO, and that an additional I atom source is required, possibly caused by the deposition of O<sub>3</sub> onto the ocean surface in the presence of solar radiation. Modelling results also show that the O<sub>3</sub> depletion observed at Cape Verde cannot be explained in the absence of halogen chemistry, which contributes ~45% of the observed O<sub>3</sub> depletion at the height of measurements (10 m) during summer. The model also predicts that halogens decrease the hydroperoxy radical (HO<sub>2</sub>) concentration by ~14% and increase the hydroxyl radical (OH) concentration by ~13% near the ocean surface. The oxidation of dimethyl sulphide (DMS) by BrO takes place at a comparable rate to oxidation by OH in this environment. Finally, the potential of iodine chemistry to form new particles is explored and conditions under which particle formation could be important in the remote MBL are discussed.
url http://www.atmos-chem-phys.net/10/4611/2010/acp-10-4611-2010.pdf
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