Air-sea fluxes of biogenic bromine from the tropical and North Atlantic Ocean
- 1Department of Chemistry, University of York, York, YO10 5DD, UK
- 2Laboratory for Global Marine and Atmospheric Chemistry, School of Environmental Sciences, University of East Anglia, Norwich, NR4 7TJ, UK
- *now at: Crichton Carbon Centre, Crichton University Campus, Dumfries, DG1 4ZL, UK
Abstract. Air-sea fluxes and bulk seawater and atmospheric concentrations of bromoform (CHBr3) and dibromomethane (CH2Br2) were measured during two research cruises in the northeast Atlantic (53–59° N, June–July 2006) and tropical eastern Atlantic Ocean including over the African coastal upwelling system (16–35° N May–June 2007). Saturations and sea-air fluxes of these compounds generally decreased in the order coastal > upwelling > shelf > open ocean, and outside of coastal regions, a broad trend of elevated surface seawater concentrations with high chlorophyll-a was observed. We show that upwelling regions (coastal and equatorial) represent regional hot spots of bromocarbons, but are probably not of major significance globally, contributing at most a few percent of the total global emissions of CHBr3 and CH2Br2. From limited data from eastern Atlantic coastlines, we tentatively suggest that globally, coastal oceans (depth <180 m) together contribute ~2.5 (1.4–3.5) Gmol Br yr−1 of CHBr3, excluding influences from anthropogenic sources such as coastal power stations. This flux estimate is close to current estimates of the total open ocean source. We also show that the concentration ratio of CH2Br2/CHBr3 in seawater is a strong function of concentration (and location), with a lower CH2Br2/CHBr3 ratio found in coastal regions near to macroalgal sources.