Bromine and iodine chemistry in a global chemistry-climate model: description and evaluation of very short-lived oceanic sources
Author:
Ordóñez C.,Lamarque J.-F.,Tilmes S.,Kinnison D. E.,Atlas E. L.,Blake D. R.,Sousa Santos G.,Brasseur G.,Saiz-Lopez A.
Abstract
Abstract. The global chemistry-climate model CAM-Chem has been extended to incorporate an expanded bromine and iodine chemistry scheme that includes natural oceanic sources of very short-lived (VSL) halocarbons, gas-phase photochemistry and heterogeneous reactions on aerosols. Ocean emissions of five VSL bromocarbons (CHBr3, CH2Br2, CH2BrCl, CHBrCl2, CHBr2Cl) and three VSL iodocarbons (CH2ICl, CH2IBr, CH2I2) have been parameterised by a biogenic chlorophyll-a (chl-a) dependent source in the tropical oceans (20° N–20° S) as well as constant oceanic fluxes with a 2.5 coast-to-ocean emission ratio for the extratropics (latitudinal bands 20°–50° and 50°–90° in both hemispheres). Top-down emission estimates of bromocarbons have been derived using available measurements in the troposphere and lower stratosphere, while iodocarbons have been constrained with observations in the marine boundary layer (MBL). Emissions of CH3I are based on a previous inventory and the longer lived CH3Br is set to a lower boundary condition. The global oceanic emissions estimated for the most abundant VSL bromocarbons – 533 Gg yr−1 for CHBr3 and 67.3 Gg yr−1 for CH2Br2 – are within the range of previous estimates. Overall the latitudinal and vertical distributions of modelled bromocarbons are in good agreement with observations. Nevertheless, we identify some issues such as the reduced number of aircraft observations to validate models in the Southern Hemisphere, the overestimation of CH2Br2 in the upper troposphere – lower stratosphere and the underestimation of CH3I in the same region. Despite the difficulties involved in the global modelling of the most short-lived iodocarbons (CH2ICl, CH2IBr, CH2I2), modelled results are in good agreement with published observations in the MBL. Finally, sensitivity simulations show that knowledge of the diurnal emission cycle for these species, in particular for CH2I2, is key to assess their global source strength.
Publisher
Copernicus GmbH
Reference98 articles.
1. Atkinson, R., Baulch, D. L., Cox, R. A., Hampson, R. F., Kerr, J. A., Rossi, M. J., and Troe, J.: Evaluated Kinetic and Photochemical Data for Atmospheric Chemistry: Supplement VIII, Halogen Species Evaluation for Atmospheric Chemistry, J. Phys. Chem. Ref. Data, 29, 167, https://doi.org/10.1063/1.556058, 2000. 2. Atkinson, R., Baulch, D. L., Cox, R. A., Crowley, J. N., Hampson Jr, R. F., Hynes, R. G., Jenkin, M. E., Kerr, J. A., Rossi, M. J., and Troe, J.: Summary of evaluated kinetic and photochemical data for atmospheric chemistry: web version February 2006, available at: http://www.iupac-kinetic.ch.cam.ac.uk, 2006. 3. Atkinson, R., Baulch, D. L., Cox, R. A., Crowley, J. N., Hampson, R. F., Hynes, R. G., Jenkin, M. E., Rossi, M. J., Troe, J., and Wallington, T. J.: Evaluated kinetic and photochemical data for atmospheric chemistry: Volume IV – gas phase reactions of organic halogen species, Atmos. Chem. Phys., 8, 4141–4496, https://doi.org/10.5194/acp-8-4141-2008, 2008. 4. Atlas, E., Pollock, W., Greenberg, J., Heidt, L., and Thompson, A. M.: Alkyl nitrates, nonmethane hydrocarbons, and halocarbon gases over the equatorial Pacific Ocean during Saga-3, J. Geophys. Res., 98, 16933–16947, 1993. 5. Baker, J. M., Sturges, W. T., Sugier, J., Sunnenberg, G., Lovett, A. A., Reeves, C. E., Nightingale, P. D., and Penkett, S. A.: Emissions of CH3Br, organochlorines, and organoiodines from temperate macroalgae, Chemosphere – Global Change Science, 3, 93–106, 2001.
Cited by
2 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
|
|