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The Habshan industrial site in the United Arab Emirates produces a regional-scale pollution plume associated with oil and gas processing, discharging high loadings of sulfates and chlorides into the atmosphere, which interact with the ambient aerosol population. Aerosol particles and trace gas chemistry at this site were studied on two flights in the summer of 2002. Measurements were collected along vertical plume profiles to show changes associated with atmospheric processing of particle and gas components. Close to the outlet stack, particle concentrations were over 10,000 cm−3, dropping to

The May 1998 transport of smoke from fires in Mexico and Central America into the United States is examined. We combine data from ground-based Interagency Monitoring of Protected Visual Environments aerosol chemical sampling sites with in situ airborne and Sun photometer measurements to develop a consistent picture of the transported smoke-impacted aerosol optical and chemical properties. The aerosol observed in Mexico and the southern United States is found to have a higher sulfate mass fraction, higher single-scattering albedo, and larger accumulation mode radius than biomass burning aerosols observed by similar instrumentation in South America and Africa. We postulate that the smoke-impacted aerosol in the 1998 event was more hygroscopic than that observed in the other locations, because of the higher mass fractions of sulfate, and show that a simple model of corresponding changes in aerosol water content yields agreement with the observed variations in refractive index and radii. We further show that the single-scattering albedo cannot be fully explained by hygroscopic growth alone. Modifications to the model invoking variations in aerosol light-absorbing carbon content, which are consistent with differences in observed composition among the various smoke-impacted aerosols, bring the predictions of single-scattering albedo into alignment with our observations. The model demonstrates that the particle size, single-scattering albedo, and real refractive index of smoke-impacted aerosols are not independent but vary in tandem with variations in particle hygroscopicity and with variations in black carbon content. This relationship is an important consideration in the assessment of the effects of biomass burning aerosols, particularly those subject to long-range transport, on radiative forcing and climate.

[1] We used conventional and environmental transmission electron microscopes to determine morphology, composition, and water uptake of individual natural inorganic aerosol particles collected from industrial pollution plumes and from clean and polluted marine environments. Five particle types are described in detail. They range from relatively insoluble mineral grains to internally mixed particles containing NaCl with other soluble or relatively insoluble material. We studied the hygroscopic behavior of these particles from 0 to 100% relative humidity (RH). Relatively insoluble materials do not take up water over the experimental RH range. Single crystals of NaCl from both natural and laboratory sources have a well-defined deliquescence point of approximately 76% RH at 291 K. NaCl-bearing aggregate particles appear to deliquesce between 74 and 76% RH (same RH within error) when NaCl is internally mixed with relatively insoluble phases, but the particles deliquesce at lower RH when aggregated with other soluble phases such as NaNO3. For all NaCl-bearing particles studied, hygroscopic growth is pronounced above 76% RH, and water uptake by the particles is dominated by the soluble phase. Furthermore, the soluble phase initiating deliquescence controls the locus of further hygroscopic growth of the aggregate particle. Our results demonstrate that composition and mixing state affect water uptake of natural aerosol particles. Furthermore, internally mixed particles are confirmed to deliquesce at lower RH values than predicted from the individual components.

[1] Episodes of regionally extensive haze were observed over southern African during the dry season intensive of the Southern African Regional Science Initiative (SAFARI 2000). Several case studies of southern African haze layers were examined and characterized in terms of physical structure as they exited off of the eastern coastal region of southern Africa. In situ observations of aerosols and trace gases and their physical and chemical characteristics were collected on board South African Weather Service Aerocommander research aircraft. Haze structure, based on these measurements, is examined as it varies with synoptic type. Despite strong differences in the observed ENSO regime between SAFARI 2000 and that observed during the Southern African Fire-Atmosphere Research Initiative (SAFARI-92) and their respective aerosol accumulation mechanisms (col Rrgions/weak anticyclones versus strong anticyclones), a surprising degree of consistency in the observed vertical structure of the lower troposphere was found in southern Africa. INDEX TERMS: 0305 Atmospheric Composition and Structure: Aerosols and particles (0345, 4801); 0345 Atmospheric Composition and Structure: Pollution—urban and regional (0305); 0365 Atmospheric Composition and Structure: Troposphere—composition and chemistry; 0368 Atmospheric Composition and Structure: Troposphere—constituent transport and chemistry; KEYWORDS: haze layers, synoptic circulations, ENSO

[1] The sources and transport of cloud condensation nuclei (CCN) over southern Africa have been investigated using in situ measurements collected during the Aerosol Recirculation and Rainfall Experiment (ARREX) wet season projects and during the Southern African Regional Science Initiative (SAFARI-2000) intensive dry season campaign. CCN concentrations over the subcontinent are generally higher in the dry season than in the wet season and exceed 2000 cm−3 in highly polluted air masses. In the late dry season, CCN concentrations are highest in the northern regions of the subcontinent due to the burning of savanna biomass. Emissions from industries and power plants on the South African Highveld are a prolific year-round source of CCN and are sufficient to account for CCN levels south of 20°S throughout the year. Most CCN are contained within the mixing layer, which extends to an altitude of 3000–4000 m over the plateau and is capped by a temperature inversion. Multiple inversions and absolutely stable layers control the stratification of aerosols and CCN. Biomass burning particles are efficient CCN, and the median diameter of the accumulation mode is large (up to 0.19 μm). Recently emitted industrial aerosols are less soluble and have a smaller median diameter (0.11 μm). Twice as many aerosols act as CCN in the dry season (68%) than in the wet season (34%). The fraction is highest in the dry season over the tropical regions (>80%), where smoke aerosol predominates. Elevated aerosol and CCN concentrations are expected to have implications for direct radiative forcing, especially in the dry season, and for indirect forcing in the wet season.