Global sea-to-air flux climatology for bromoform, dibromomethane and methyl iodide

Volatile halogenated organic compounds containing bromine and iodine, which are naturally produced in the ocean, are involved in ozone depletion in both the troposphere and stratosphere. Three prominent compounds transporting large amounts of marine halogens into the atmosphere are bromoform (CHBr3)...

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Published in:Atmospheric Chemistry and Physics
Main Authors: Ziska, F., Quack, B., Abrahamsson, K., Archer, S. D., Atlas, E., Bell, T., Butler, J. H., Carpenter, L. J., Jones, C. E., Harris, N. R. P., Hepach, H., Heumann, K. G., Hughes, C., Kuss, J., Krüger, K., Liss, P., Moore, R. M., Orlikowska, A., Raimund, S., Reeves, C. E., Reifenhäuser, W., Robinson, A. D., Schall, C., Tanhua, T., Tegtmeier, S., Turner, S., Wang, L., Wallace, D., Williams, J., Yamamoto, H., Yvon-Lewis, S., Yokouchi, Y.
Format: Article in Journal/Newspaper
Language:unknown
Published: 2013
Subjects:
Online Access:https://ueaeprints.uea.ac.uk/id/eprint/44228/
https://doi.org/10.5194/acp-13-8915-2013
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spelling ftuniveastangl:oai:ueaeprints.uea.ac.uk:44228 2023-08-27T04:06:03+02:00 Global sea-to-air flux climatology for bromoform, dibromomethane and methyl iodide Ziska, F. Quack, B. Abrahamsson, K. Archer, S. D. Atlas, E. Bell, T. Butler, J. H. Carpenter, L. J. Jones, C. E. Harris, N. R. P. Hepach, H. Heumann, K. G. Hughes, C. Kuss, J. Krüger, K. Liss, P. Moore, R. M. Orlikowska, A. Raimund, S. Reeves, C. E. Reifenhäuser, W. Robinson, A. D. Schall, C. Tanhua, T. Tegtmeier, S. Turner, S. Wang, L. Wallace, D. Williams, J. Yamamoto, H. Yvon-Lewis, S. Yokouchi, Y. 2013-09-06 https://ueaeprints.uea.ac.uk/id/eprint/44228/ https://doi.org/10.5194/acp-13-8915-2013 unknown Ziska, F., Quack, B., Abrahamsson, K., Archer, S. D., Atlas, E., Bell, T., Butler, J. H., Carpenter, L. J., Jones, C. E., Harris, N. R. P., Hepach, H., Heumann, K. G., Hughes, C., Kuss, J., Krüger, K., Liss, P., Moore, R. M., Orlikowska, A., Raimund, S., Reeves, C. E., Reifenhäuser, W., Robinson, A. D., Schall, C., Tanhua, T., Tegtmeier, S., Turner, S., Wang, L., Wallace, D., Williams, J., Yamamoto, H., Yvon-Lewis, S. and Yokouchi, Y. (2013) Global sea-to-air flux climatology for bromoform, dibromomethane and methyl iodide. Atmospheric Chemistry and Physics, 13 (17). pp. 8915-8934. doi:10.5194/acp-13-8915-2013 Article PeerReviewed 2013 ftuniveastangl https://doi.org/10.5194/acp-13-8915-2013 2023-08-03T22:32:05Z Volatile halogenated organic compounds containing bromine and iodine, which are naturally produced in the ocean, are involved in ozone depletion in both the troposphere and stratosphere. Three prominent compounds transporting large amounts of marine halogens into the atmosphere are bromoform (CHBr3), dibromomethane (CH2Br2) and methyl iodide (CH3I). The input of marine halogens to the stratosphere has been estimated from observations and modelling studies using low-resolution oceanic emission scenarios derived from top-down approaches. In order to improve emission inventory estimates, we calculate data-based high resolution global sea-to-air flux estimates of these compounds from surface observations within the HalOcAt (Halocarbons in the Ocean and Atmosphere) database (https://halocat.geomar.de/). Global maps of marine and atmospheric surface concentrations are derived from the data which are divided into coastal, shelf and open ocean regions. Considering physical and biogeochemical characteristics of ocean and atmosphere, the open ocean water and atmosphere data are classified into 21 regions. The available data are interpolated onto a 1°×1° grid while missing grid values are interpolated with latitudinal and longitudinal dependent regression techniques reflecting the compounds' distributions. With the generated surface concentration climatologies for the ocean and atmosphere, global sea-to-air concentration gradients and sea-to-air fluxes are calculated. Based on these calculations we estimate a total global flux of 1.5/2.5 Gmol Br yr−1 for CHBr3, 0.78/0.98 Gmol Br yr−1 for CH2Br2 and 1.24/1.45 Gmol Br yr−1 for CH3I (robust fit/ordinary least squares regression techniques). Contrary to recent studies, negative fluxes occur in each sea-to-air flux climatology, mainly in the Arctic and Antarctic regions. "Hot spots" for global polybromomethane emissions are located in the equatorial region, whereas methyl iodide emissions are enhanced in the subtropical gyre regions. Inter-annual and seasonal variation is ... Article in Journal/Newspaper Antarc* Antarctic Arctic University of East Anglia: UEA Digital Repository Antarctic Arctic Atmospheric Chemistry and Physics 13 17 8915 8934
institution Open Polar
collection University of East Anglia: UEA Digital Repository
op_collection_id ftuniveastangl
language unknown
description Volatile halogenated organic compounds containing bromine and iodine, which are naturally produced in the ocean, are involved in ozone depletion in both the troposphere and stratosphere. Three prominent compounds transporting large amounts of marine halogens into the atmosphere are bromoform (CHBr3), dibromomethane (CH2Br2) and methyl iodide (CH3I). The input of marine halogens to the stratosphere has been estimated from observations and modelling studies using low-resolution oceanic emission scenarios derived from top-down approaches. In order to improve emission inventory estimates, we calculate data-based high resolution global sea-to-air flux estimates of these compounds from surface observations within the HalOcAt (Halocarbons in the Ocean and Atmosphere) database (https://halocat.geomar.de/). Global maps of marine and atmospheric surface concentrations are derived from the data which are divided into coastal, shelf and open ocean regions. Considering physical and biogeochemical characteristics of ocean and atmosphere, the open ocean water and atmosphere data are classified into 21 regions. The available data are interpolated onto a 1°×1° grid while missing grid values are interpolated with latitudinal and longitudinal dependent regression techniques reflecting the compounds' distributions. With the generated surface concentration climatologies for the ocean and atmosphere, global sea-to-air concentration gradients and sea-to-air fluxes are calculated. Based on these calculations we estimate a total global flux of 1.5/2.5 Gmol Br yr−1 for CHBr3, 0.78/0.98 Gmol Br yr−1 for CH2Br2 and 1.24/1.45 Gmol Br yr−1 for CH3I (robust fit/ordinary least squares regression techniques). Contrary to recent studies, negative fluxes occur in each sea-to-air flux climatology, mainly in the Arctic and Antarctic regions. "Hot spots" for global polybromomethane emissions are located in the equatorial region, whereas methyl iodide emissions are enhanced in the subtropical gyre regions. Inter-annual and seasonal variation is ...
format Article in Journal/Newspaper
author Ziska, F.
Quack, B.
Abrahamsson, K.
Archer, S. D.
Atlas, E.
Bell, T.
Butler, J. H.
Carpenter, L. J.
Jones, C. E.
Harris, N. R. P.
Hepach, H.
Heumann, K. G.
Hughes, C.
Kuss, J.
Krüger, K.
Liss, P.
Moore, R. M.
Orlikowska, A.
Raimund, S.
Reeves, C. E.
Reifenhäuser, W.
Robinson, A. D.
Schall, C.
Tanhua, T.
Tegtmeier, S.
Turner, S.
Wang, L.
Wallace, D.
Williams, J.
Yamamoto, H.
Yvon-Lewis, S.
Yokouchi, Y.
spellingShingle Ziska, F.
Quack, B.
Abrahamsson, K.
Archer, S. D.
Atlas, E.
Bell, T.
Butler, J. H.
Carpenter, L. J.
Jones, C. E.
Harris, N. R. P.
Hepach, H.
Heumann, K. G.
Hughes, C.
Kuss, J.
Krüger, K.
Liss, P.
Moore, R. M.
Orlikowska, A.
Raimund, S.
Reeves, C. E.
Reifenhäuser, W.
Robinson, A. D.
Schall, C.
Tanhua, T.
Tegtmeier, S.
Turner, S.
Wang, L.
Wallace, D.
Williams, J.
Yamamoto, H.
Yvon-Lewis, S.
Yokouchi, Y.
Global sea-to-air flux climatology for bromoform, dibromomethane and methyl iodide
author_facet Ziska, F.
Quack, B.
Abrahamsson, K.
Archer, S. D.
Atlas, E.
Bell, T.
Butler, J. H.
Carpenter, L. J.
Jones, C. E.
Harris, N. R. P.
Hepach, H.
Heumann, K. G.
Hughes, C.
Kuss, J.
Krüger, K.
Liss, P.
Moore, R. M.
Orlikowska, A.
Raimund, S.
Reeves, C. E.
Reifenhäuser, W.
Robinson, A. D.
Schall, C.
Tanhua, T.
Tegtmeier, S.
Turner, S.
Wang, L.
Wallace, D.
Williams, J.
Yamamoto, H.
Yvon-Lewis, S.
Yokouchi, Y.
author_sort Ziska, F.
title Global sea-to-air flux climatology for bromoform, dibromomethane and methyl iodide
title_short Global sea-to-air flux climatology for bromoform, dibromomethane and methyl iodide
title_full Global sea-to-air flux climatology for bromoform, dibromomethane and methyl iodide
title_fullStr Global sea-to-air flux climatology for bromoform, dibromomethane and methyl iodide
title_full_unstemmed Global sea-to-air flux climatology for bromoform, dibromomethane and methyl iodide
title_sort global sea-to-air flux climatology for bromoform, dibromomethane and methyl iodide
publishDate 2013
url https://ueaeprints.uea.ac.uk/id/eprint/44228/
https://doi.org/10.5194/acp-13-8915-2013
geographic Antarctic
Arctic
geographic_facet Antarctic
Arctic
genre Antarc*
Antarctic
Arctic
genre_facet Antarc*
Antarctic
Arctic
op_relation Ziska, F., Quack, B., Abrahamsson, K., Archer, S. D., Atlas, E., Bell, T., Butler, J. H., Carpenter, L. J., Jones, C. E., Harris, N. R. P., Hepach, H., Heumann, K. G., Hughes, C., Kuss, J., Krüger, K., Liss, P., Moore, R. M., Orlikowska, A., Raimund, S., Reeves, C. E., Reifenhäuser, W., Robinson, A. D., Schall, C., Tanhua, T., Tegtmeier, S., Turner, S., Wang, L., Wallace, D., Williams, J., Yamamoto, H., Yvon-Lewis, S. and Yokouchi, Y. (2013) Global sea-to-air flux climatology for bromoform, dibromomethane and methyl iodide. Atmospheric Chemistry and Physics, 13 (17). pp. 8915-8934.
doi:10.5194/acp-13-8915-2013
op_doi https://doi.org/10.5194/acp-13-8915-2013
container_title Atmospheric Chemistry and Physics
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