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Detailed Reference Information |
Gong, S.L. and Barrie, L.A. (2003). Simulating the impact of sea salt on global nss sulphate aerosols. Journal of Geophysical Research 108: doi: 10.1029/2002JD003181. issn: 0148-0227. |
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The Canadian Aerosol Module coupled with the Canadian third generation Global Climate Model was used to simulate the global distributions of size-segregated sea salt and sulphate aerosols of both anthropogenic and natural origins in the atmosphere. A sectional model of 12 size bins was used to treat the size distribution of sea salt and sulphate, which is assumed to be internally mixed in each size bin. The spatial and temporal distributions predicted by the model compare reasonably well with observations. The mixed aerosol simulations yield number and volume size distributions in the marine boundary layer (MBL) comparable with observations. Sea salt particles redistribute the mass and number distributions of sulphate aerosols by serving as a quenching agent to nucleation and as an additional surface area for condensation and by changing the cloud properties in the MBL. By differential simulations of global sea salt and sulphate it is found that the presence of sea salt increases the mass mean diameter of sulphate aerosols by up to a factor of 2 over the MBL with high sea salt concentrations and reduces the global sulphate aerosol mass in the surface MBL layer from 5 to 75% depending on the sea salt distributions. The high impacts are in the midlatitudes of both Northern and Southern Hemispheres with a minimum in the equatorial regions. In the polluted anthropogenic regions of North Pacific and Atlantic, sea salt reduces the sulphate concentration from 10 to 30%. The peak reductions of 50--75% occur in the roaring 40s of the Southern Hemisphere in spring and fall. The impact of sea salt on the annual global mass and number loading is estimated to be 9.13 and 0.76%, respectively. A reduction of 20--60% in the marine cloud droplet number concentrations (CDNC) was predicted because of the presence of sea salt, with greatest reductions in the roaring 40s south (40--70%) and in the midlatitude north (20--40%) where the sea salt concentrations were high. Along the equatorial regions some enhancement of total CDNC was simulated because of the presence of sea salt aerosols. |
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Abstract |
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Keywords
Atmospheric Composition and Structure, Aerosols and particles (0345, 4801), Atmospheric Composition and Structure, Cloud physics and chemistry, Meteorology and Atmospheric Dynamics, Ocean/atmosphere interactions (0312, 4504) |
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Publisher
American Geophysical Union 2000 Florida Avenue N.W. Washington, D.C. 20009-1277 USA 1-202-462-6900 1-202-328-0566 service@agu.org |
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