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Meteorological Service of Canada Environment Canada The Global Cycling Of Size- distributed Sea-salt Particles And Their Influence On Sulphate Aerosols Sun Ling Gong 1 and Leonard A. Barrie 2 1 Air Quality Research Branch, Meteorological Service of Canada, 4905 Dufferin Street, Toronto, Ontario M3H 5T4, CANADA 2 Environment Division, AREP, World Meteorological Organization, 7 bis, Avenue de la Paix, BP2300, 1211 Geneva 2 WMO

The Global Cycling Of Size-distributed Sea-salt Particles And Their Influence On Sulphate Aerosols

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WMO. The Global Cycling Of Size-distributed Sea-salt Particles And Their Influence On Sulphate Aerosols. - PowerPoint PPT Presentation

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  • CAM: A Size Segregated Simulation of Atmospheric Aerosol Processes for Climate and Air Quality Models J. Geophy. Res. 2002 (in press)1.Module Development

    S.L. Gong1, L.A. Barrie2, J.-P. Blanchet3, K. von Salzen5, U. Lohmann4, G. Lesins4, L. Spacek3, L.M. Zhang1, E. Girard3, H. Lin1, R. Leaitch1, H. Leighton5, P. Chylek4 and P. Huang12. Global sea-salt aerosol and its budgetsS.L. Gong1, L.A. Barrie2 and M. Lazare1

  • Model Configurations CAM/GCM

    Aerosols

    12 bin sectional model: r=0.005 20.48 m [dry]

    Sources

    GEIA 1B: 2-level anthropogenic SO2 and SO4

    Kettle et al. : Surface DMS concentration

    Benkovitz et al. : H2S monthly mean flux

    Gong et al. : Sea-salt surface flux

    Prognostic

    Variables

    Sea-salt and sulphate mass mixing ratio in each size bin, cloud water and ice, DMS, SO2, H2S and H2SO4[g]

    Clear-sky

    processes

    Nucleation, condensation, coagulation, on-line S chemistry with MOZARTs OH and NO3

    Wet

    Processes

    Gong et al : Below-cloud scavenging

    Lohmann : Explicit cloud scheme

    Cloud activation and cloud S chemistry with MOZARTs O3, H2O2 and HNO3, and NH3

    Dry Deposition

    Size-dependent particle and SO2

    Resolution

    96(48(22, 20 min

  • Global Sea-salt Simulations and Budgets

  • Global Sea-salt Concentrations

  • Global Sea-salt Compared with ObservationsComparison Sites [WCRP/IGAC COSAM]

  • Sea-salt Size Distributions(d) Model 197 hPa(b) Quinn et al. [1996] Surface(c) Model 698 hPa(a) Model 995 hPaCompare

  • Global Sea-salt Residence Times - Coarse

  • Global Sea-salt Residence Times - Fine

  • Annual Global Sea-salt Budgets 1012 kggiga-ton

  • Global Monthly Sea-salt Emissions

  • Global Sulphate Aerosols Influenced by Sea-salt

  • Global Sulphate Concentrations

  • Global Sulphate Compared with ObservationsComparison Sites [WCRP/IGAC COSAM]

  • Volume Size DistributionsQuinn et al. 1996Simulations140W, 40S

  • Global Sulphate Distributions

  • Surface Reduction of Sulphate by Sea-salt-20~30%-50~70%-20~30%Rosenfeld et al 2002, ScienceSea-salt cleans air pollution-10~20%

  • Mechanisms of the Sea-salt Impact (1)Cleaning AgentsCondensation of sulphuric acid vapour onto existing sea-salt particles reduces the atmospheric sulphate cycling time and hence reduces the sulphate concentrations.Sea-salt aerosols override the precipitation suppression effects of the large number of small pollution nuclei.

  • Impact of Sea-salt on Sulphate Number Size Distributions Sea-salt reduces the number concentration of sulphate by enhancing condensation and coagulations.

  • Mass-mean Diameters of Sulphate (MAM)Increases in MMD reduce the residence time and hence concentrations of sulphate.

  • Mechanisms of the Sea-salt Impact (2)Effects on CloudsSea-salt provides additional CCN for SO2 in-cloud oxidation and hence increases the sulphate concentrations.An increase more than 20% in in-cloud sulphate production due to additional sea-salt particles and higher pH associated with newly formed sea-salt-nucleated cloud droplets compared to sulphate. [ODowd et al. 1997, Lowe et al. 1995]

  • Sea-salt on cloud droplet number[Pszenny et al 1998][ODowd et al. 1999][Rosenfeld et al 2002]Sea-salt aerosols override the precipitation suppression effects of the large number of small pollution nuclei.

    The enhancement in precipitation helps remove pollution.

  • Changes of Sulphate MMR by Sea-salt10~20%Competitive processes of sea-salt with positive and negative effects on sulphate.

    Location dependent.

  • ConclusionsThe global annual sea-salt emission to the atmosphere is about 1.011013 kg with 68% in the southern hemisphere.

    Residence times of 7.7 mm and 0.4 mm diameter sea salt particles in the marine boundary layer were in the range 0.3 - 10 hours and 80 360 hours, respectively.

    By serving as a quenching agent to nucleation and additional surface area for condensation, sea-salt aerosols increase the mass mean diameter of sulphate aerosols by a factor of 2 and reduce the global sulphate aerosol mass in the surface MBL layer from 5 to 75% for most of the open oceans.