Inorganic bromine in the marine boundary layer: a critical review

R. Sander (1) , W. C. Keene (2) , A. A. P. Pszenny (3) , R. Arimoto (4) , G. P. Ayers (5) , E. Baboukas (1) , J. M. Cainey (6) , P. J. Crutzen (1) , R. A. Duce (7, 8) , G. Hönninger (9) , B. J. Huebert (10) , W. Maenhaut (11) , N. Mihalopoulos (12) , V. C. Turekian (13) , R. van Dingenen (14)

1 Atmospheric Chemistry Department [MPIC]
2 Department of Environmental Sciences
3 Center for Global Change Science
4 CEMRC/New Mexico State University
5 CSIRO Atmospheric Research
6 Cape Grim Baseline Air Pollution Station
7 Department of Atmospheric Sciences [College Station]
8 Department of Oceanography [College Station]
9 Institut für Umweltphysik [Heidelberg]
10 Department of Oceanography
11 Department of Analytical Chemistry [Ghent]
12 ECPL - Environmental Chemical Processes Laboratory [Heraklion]
13 National Academy of Sciences
14 JRC - European Commission - Joint Research Centre [Ispra]

The cycling of inorganic bromine in the marine boundary layer (mbl) has received increased attention in recent years. Bromide, a constituent of sea water, is injected into the atmosphere in association with sea-salt aerosol by breaking waves on the ocean surface. Measurements reveal that supermicrometer sea-salt aerosol is depleted in bromine by about 50% relative to conservative tracers, whereas marine submicrometer aerosol is often enriched in bromine. Model calculations, laboratory studies, and field observations strongly suggest that these depletions reflect the chemical transformation of particulate bromide to reactive inorganic gases that influence the processing of ozone and other important constituents of marine air. However, currently available techniques cannot reliably quantify many \chem{Br}-containing compounds at ambient concentrations and, consequently, our understanding of inorganic Br cycling over the oceans and its global significance are uncertain. To provide a more coherent framework for future research, we have reviewed measurements in marine aerosol, the gas phase, and in rain. We also summarize sources and sinks, as well as model and laboratory studies of chemical transformations. The focus is on inorganic bromine over the open oceans, excluding the polar regions. The generation of sea-salt aerosol at the ocean surface is the major tropospheric source producing about 6.2 Tg/a of bromide. The transport of Br from continents (as mineral aerosol, and as products from biomass-burning and fossil-fuel combustion) can be of local importance. Transport of degradation products of long-lived Br-containing compounds from the stratosphere and other sources contribute lesser amounts. Available evidence suggests that, following aerosol acidification, sea-salt bromide reacts to form Br₂ and BrCl that volatilize to the gas phase and photolyze in daylight to produce atomic Br and Cl. Subsequent transformations can destroy tropospheric ozone, oxidize dimethylsulfide (DMS) and hydrocarbons in the gas phase and S(IV) in aerosol solutions, and thereby potentially influence climate. The diurnal cycle of gas-phase \Br and the corresponding particulate Br deficits are correlated. Higher values of Br in the gas phase during daytime are consistent with expectations based on photochemistry. Mechanisms that explain the widely reported accumulation of particulate Br in submicrometer aerosols are not yet understood. We expect that the importance of inorganic Br cycling will vary in the future as a function of both increasing acidification of the atmosphere (through anthropogenic emissions) and climate changes. The latter affects bromine cycling via meteorological factors including global wind fields (and the associated production of sea-salt aerosol), temperature, and relative humidity.

Domaines: Océan, Atmosphère

R. Sander, W. C. Keene, A. A. P. Pszenny, R. Arimoto, G. P. Ayers, et al.. Inorganic bromine in the marine boundary layer: a critical review. Atmospheric Chemistry and Physics Discussions, 2003, 3 (3), pp.2963-3050. ⟨hal-00301099⟩