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Cross-hemispheric transport of central African biomass burning pollutants: implications for downwind ozone production

Pollutant plumes with enhanced levels of trace gases and aerosols were observed over the southern coast of West Africa during August 2006 as part of the AMMA wet season field campaign. Plumes were observed both in the mid and upper troposphere. In this study we examined both the origin of these poll...

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Bibliographic Details
Published in:Atmospheric chemistry and physics discussions 2009-08, Vol.9 (4), p.17385-17427
Main Authors: Real, E, Volk, M, McQuaid, J B, Stewart, D J, Lee, J, Lewis, A, Hopkins, J R, Ravegnani, F, Ulanovski, A, Liousse, C, Orlandi, E, Law, K S, Fierli, F, Josset, D, Cairo, F, Schlager, H, Borrmann, S, Kunkel, D
Format: Article
Language:English
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Summary:Pollutant plumes with enhanced levels of trace gases and aerosols were observed over the southern coast of West Africa during August 2006 as part of the AMMA wet season field campaign. Plumes were observed both in the mid and upper troposphere. In this study we examined both the origin of these pollutant plumes and their potential to produce O sub(3) downwind over the Atlantic Ocean. Runs using the BOLAM mesoscale model including biomass burning CO tracers were used to confirm an origin from central African fires. The plumes in the mid troposphere had significantly higher pollutant concentrations due to the fact that transport occurred from a region nearer or even over the fire region. In contrast, plumes transported into the upper troposphere over West Africa had been transported to the north-east of the fire region before being uplifted. Modelled tracer results showed that pollutants resided for between 9 and 12 days over Central Africa before being transported for 4 days, in the case of the mid-troposphere plume and 2 days in the case of the upper tropospheric plume to the measurement location over the southern part of West Africa. Around 35% of the biomass burning tracer was transported into the upper troposphere compared to that remaining in the mid troposphere. Runs using a photochemical trajectory model, CiTTyCAT, were used to estimate the net photochemical O sub(3) production potential of these plumes. The mid tropospheric plume was still very photochemically active (up to 7 ppbv/day) especially during the first few days of transport westward over the Atlantic Ocean. The upper tropospheric plume was also still photochemically active, although at a slower rate (1-2 ppbv/day). Trajectories show this plume being recirculated around an upper tropospheric anticyclone back towards the African continent (around 20 S). The potential of theses plumes to produce O sub(3) supports the hypothesis that biomass burning pollutants are contributing to the observed O sub(3) maxima over the southern Atlantic at this time of year.
ISSN:1680-7367
1680-7375