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Multi-model simulations of the impact of international shipping on Atmospheric Chemistry and Climate in 2000 and 2030

Eyring, V. and Stevenson, D. S. and Lauer, A. and Dentener, F. J. and Butler, T. and Collins, W. J. and Ellingsen, K. and Gauss, M. and Hauglustaine, D. A. and Isaksen, I. S. A. and Lawrence, M. G. and Richter, A. and Rodriguez, J. M. and Sanderson, M. and Strahan, S. E. and Sudo, K. and Szopa, S. and van Noije, T. P. C. and Wild, O. (2007) Multi-model simulations of the impact of international shipping on Atmospheric Chemistry and Climate in 2000 and 2030. Atmospheric Chemistry and Physics, 7. pp. 757-780. ISSN 1680-7316

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    Abstract

    The global impact of shipping on atmospheric chemistry and radiative forcing, as well as the associated uncertainties, have been quantified using an ensemble of ten state-of-the-art atmospheric chemistry models and a predefined set of emission data. The analysis is performed for present-day conditions ( year 2000) and for two future ship emission scenarios. In one scenario ship emissions stabilize at 2000 levels; in the other ship emissions increase with a constant annual growth rate of 2.2% up to 2030 ( termed the "Constant Growth Scenario" (CGS)). Most other anthropogenic emissions follow the IPCC ( Intergovernmental Panel on Climate Change) SRES ( Special Report on Emission Scenarios) A2 scenario, while biomass burning and natural emissions remain at year 2000 levels. An intercomparison of the model results with observations over the Northern Hemisphere (25 degrees - 60 degrees N) oceanic regions in the lower troposphere showed that the models are capable to reproduce ozone (O-3) and nitrogen oxides (NOx= NO+ NO2) reasonably well, whereas sulphur dioxide (SO2) in the marine boundary layer is significantly underestimated. The most pronounced changes in annual mean tropospheric NO2 and sulphate columns are simulated over the Baltic and North Seas. Other significant changes occur over the North Atlantic, the Gulf of Mexico and along the main shipping lane from Europe to Asia, across the Red and Arabian Seas. Maximum contributions from shipping to annual mean near-surface O-3 are found over the North Atlantic ( 5 - 6 ppbv in 2000; up to 8 ppbv in 2030). Ship contributions to tropospheric O3 columns over the North Atlantic and Indian Oceans reach 1 DU in 2000 and up to 1.8 DU in 2030. Tropospheric O-3 forcings due to shipping are 9.8 +/- 2.0 mW/m(2) in 2000 and 13.6 +/- 2.3 mW/m(2) in 2030. Whilst increasing O-3, ship NOx simultaneously enhances hydroxyl radicals over the remote ocean, reducing the global methane lifetime by 0.13 yr in 2000, and by up to 0.17 yr in 2030, introducing a negative radiative forcing. The models show future increases in NOx and O-3 burden which scale almost linearly with increases in NOx emission totals. Increasing emissions from shipping would significantly counteract the benefits derived from reducing SO2 emissions from all other anthropogenic sources under the A2 scenario over the continents, for example in Europe. Globally, shipping contributes 3% to increases in O-3 burden between 2000 and 2030, and 4.5% to increases in sulphate under A2/CGS. However, if future ground based emissions follow a more stringent scenario, the relative importance of ship emissions will increase. Inter-model differences in the simulated O-3 contributions from ships are significantly smaller than estimated uncertainties stemming from the ship emission inventory, mainly the ship emission totals, the distribution of the emissions over the globe, and the neglect of ship plume dispersion.

    Item Type: Article
    Journal or Publication Title: Atmospheric Chemistry and Physics
    Uncontrolled Keywords: MARINE BOUNDARY-LAYER ; STRATOSPHERE-TROPOSPHERE EXCHANGE ; GLOBAL 3-DIMENSIONAL MODEL ; NONMETHANE HYDROCARBONS ; OZONE SIMULATIONS ; EMISSION CONTROLS ; TRANSPORT MODELS ; CHEMICAL-MODEL ; SHIPS ; AIRCRAFT
    Subjects:
    Departments: Faculty of Science and Technology > Lancaster Environment Centre
    ID Code: 49576
    Deposited By: ep_importer_pure
    Deposited On: 07 Sep 2011 11:17
    Refereed?: Yes
    Published?: Published
    Last Modified: 06 Sep 2013 22:28
    Identification Number:
    URI: http://eprints.lancs.ac.uk/id/eprint/49576

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