Atmospheric Chemistry and Physics www.atmos-chem-phys.net 1680-7316 1680-7324 5 11 2005 10.5194/acp-5-2927-2005 http://www.atmos-chem-phys.net/5/2927/2005/ http://www.atmos-chem-phys.net/5/2927/2005/acp-5-2927-2005.html http://www.atmos-chem-phys.net/5/2927/2005/acp-5-2927-2005.pdf 2927 2934 2005-11-02 Atmospheric bromoform at Mace Head, Ireland: seasonality and evidence for a peatland source L. J. Carpenter D. J. Wevill S. O'Doherty G. Spain P. G. Simmonds Department of Chemistry, University of York, York, YO10 5DD, UK School of Chemistry, University of Bristol, Bristol, BS8 1TS, UK Department of Physics, NUIGalway, Galway, Ireland In situ atmospheric observations of bromoform (CHBr₃) made over a 2.5 year period at Mace Head, Ireland from May 2001- Dec 2003, including during the NAMBLEX (North Atlantic Marine Boundary Layer Experiment) campaign, show broad maxima from spring until autumn and winter minima, with mixing ratios of 5.3+1.0 pptv (mid March - mid October) and 1.8+0.8 pptv (December-February). This indicates that, unlike CHCl₃, which has a summer minimum and winter maximum at Mace Head, local biological sources of CHBr₃ have a greater influence on the atmospheric data than photochemical decay during long-range transport. The emission sources are predominantly macroalgal, but we find evidence for a small terrestrial flux from peatland ecosystems, which so far has not been accounted for in the CHBr₃ budget. Sharp increases in CHCl₃ and CHBr₃ concentrations and decreases in O₃ concentrations occurred at night when the wind direction switched from an ocean- to a land-based sector (land breeze) and the wind speed dropped to below 5 ms^-1. These observations infer a shallow atmospheric boundary layer with increased O₃ deposition and concentration of local emissions of both CHCl₃ and CHBr₃. The ratio of ΔCHCl₃/ΔCHBr₃ varied strongly according to the prevailing wind direction; from 0.60+0.15 in south-easterly (100-170° and northerly (340-20°) air to 2.5+0.4 in north-easterly (40-70°) air. Of these land-sectors, the south-easterly air masses are likely to be strongly influenced by macroalgal beds along the coast and the emission ratios probably reflect those from seaweeds in addition to land sources. The north-easterly airmasses however had an immediate fetch inland, which locally is comprised of coastal peatland ecosystems (peat bogs and coastal conifer plantations), previously identified as being strong sources of atmospheric CHCl₃ under these conditions. Although we cannot entirely rule out other local land or coastal sources, our observations also suggest peatland ecosystem emissions of CHBr₃. We use correlations between CHCl₃ and CHBr₃ during the north-easterly land breeze events in conjunction with previous estimates of local wetland CHCl₃ release to tentatively deduce a global wetland CHBr₃ source of 20.4(0.4-948) Gg yr^-1, which is approximately 7% of the total global source.