Abstract. On April 15 and 19, 1998, two intense dust storms were generated over the Gobi desert by springtime low-pressure systems descending from the northwest. The windblown dust was detected and its evolution followed by its yellow color on SeaWiFS satellite images, routine surface-based monitoring, and through serendipitous observations. The April 15 dust cloud was recirculating, and it was removed by a precipitating weather system over east Asia

[1] The Model for Integrated Research on Atmospheric Global Exchanges (MIRAGE) modeling system, designed to study the impacts of anthropogenic aerosols on the global environment, is described. MIRAGE consists of a chemical transport model coupled online with a global climate model. The chemical transport model simulates trace gases, aerosol number, and aerosol chemical component mass (sulfate, methane sulfonic acid (MSA), organic matter, black carbon (BC), sea salt, and mineral dust) for four aerosol modes (Aitken, accumulation, coarse sea salt, and coarse mineral dust) using the modal aerosol dynamics approach. Cloud-phase and interstitial aerosol are predicted separately. The climate model, based on Community Climate Model, Version 2 (CCM2), has physically based treatments of aerosol direct and indirect forcing. Stratiform cloud water and droplet number are simulated using a bulk microphysics parameterization that includes aerosol activation. Aerosol and trace gas species simulated by MIRAGE are presented and evaluated using surface and aircraft measurements. Surface-level SO 2 in North American and European source regions is higher than observed. SO 2 above the boundary layer is in better agreement with observations, and surface-level SO 2 at marine locations is somewhat lower than observed. Comparison with other models suggests insufficient SO 2 dry deposition; increasing the deposition velocity improves simulated SO 2 . Surface-level sulfate in North American and European source regions is in good agreement with observations, although the seasonal cycle in Europe is stronger than observed. Surface-level sulfate at high-latitude and marine locations, and sulfate above the boundary layer, are higher than observed. This is attributed primarily to insufficient wet removal; increasing the wet removal improves simulated sulfate at remote locations and aloft. Because of the high sulfate bias, radiative forcing estimates for anthropogenic sulfur given in 2001 by S. J. Ghan and colleagues are probably too high. Surface-level dimethyl sulfide (DMS) is $40% higher than observed, and the seasonal cycle shows too much DMS in local winter, partially caused by neglect of oxidation by NO 3 . Surface-level MSA at marine locations is $80% higher than observed, also attributed to insufficient wet removal. Surface-level BC is $50% lower than observed in the United States and $40% lower than observed globally. Treating BC as initially hydrophobic would lessen this bias. Surface-level organic matter is lower than observed in the United States, similar to BC, but shows no bias in the global comparison. Surface-level sea salt concentrations are $30% lower than observed, partly caused by low temporal variance of the model's 10 m wind speeds. Submicrometer sea salt is strongly underestimated by the emissions parameterization. Dust concentrations are within a factor of 3 at most sites but tend to be lower than observed, primarily because of neglect of very large particles and underestimation of emissions and vertical transport under ...

Anthropogenic aerosols are composed of a variety of aerosol types and components including water-soluble inorganic species (e.g., sulfate, nitrate, ammonium), condensed organic species, elemental or black carbon, and mineral dust. Previous estimates of the clear sky forcing by anthropogenic sulfate aerosols and by organic biomass-burning aerosols indicate that this forcing is of sufficient magnitude to mask the effects of anthropogenic greenhouse gases over large regions. Here, the uncertainty in the forcing by these aerosol types is estimated. The clear sky forcing by other anthropogenic aerosol components cannot be estimated with confidence, although the forcing by these aerosol types appears to be smaller than that by sulfate and biomass-burning aerosols.The cloudy sky forcing by anthropogenic aerosols, wherein aerosol cloud condensation nuclei concentrations are increased, thereby increasing cloud droplet concentrations and cloud albedo and possibly influencing cloud persistence, may also be significant. In contrast to the situation with the clear sky forcing, estimates of the cloudy sky forcing by anthropogenic aerosols are little more than guesses, and it is not possible to quantify the uncertainty of the estimates.In view of present concerns over greenhouse gas-induced climate change, this situation dictates the need to quantify the forcing by anthropogenic aerosols and to define and minimize uncertainties in the calculated forcings. In this article, a research strategy for improving the estimates of the clear sky forcing is defined. The strategy encompasses five major, and necessarily coordinated, activities: surface-based observations of aerosol chemical and physical properties and their influence on the radiation field; aircraft-based observations of the same properties; process studies to refine model

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Abstract. Estimates of direct and indirect radiative forcing by anthropogenic sulfate aerosols from an integrated global aerosol and climate modeling system are presented. A detailed global tropospheric chemistry and aerosol model that predicts concentrations of oxidants as well as aerosols and aerosol precursors, is coupled to a general circulation model that predicts both cloud water mass and cloud droplet number. Both number and mass of several externally mixed aerosol size modes are predicted, with internal mixing assumed for the different aerosol components within each mode. Predicted aerosol species include sulfate, organic and black carbon, soil dust, and sea salt. The models use physically based treatments of aerosol radiative properties (including dependence on relative humidity) and aerosol activation as cloud condensation nuclei. Parallel simulations with and without anthropogenic sulfate aerosol are performed for a global domain. The global and annual mean direct and indirect radiative forcing due to anthropogenic sulfate are estimated to be -0.3 to -0.5 and -1.5 to -3.0 W rn '2, respectively. The radiative forcing is sensitive to the model's horizontal resolution, the use of predicted versus analyzed relative humidity, the prediction versus diagnosis of aerosol number and droplet number, and the parameterization of droplet collision/ coalescence. About half of the indirect radiative forcing is due to changes in droplet radius and half to increased cloud liquid water.