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Aerosol loading over Interior Alaska displays a strong seasonality, with pristine conditions generally prevailing during winter months. Long term aerosol research from the University of Alaska Fairbanks indicates that the period around April typically marks the beginning of the transition from winter to summer conditions. In April 2008, the NASA-sponsored "Arctic Research of the Composition of the Troposphere from Aircraft and Satellites" (ARCTAS) field campaign was conducted to analyze incursions of aerosols transported over Alaska and the Canadian North. In and around Fairbanks, Alaska, data concerning aerosol characteristics were gathered by polarization (0.693 μm) lidar, DRUM Impactor sampler, and balloon-borne optical particle counter. These data provide information on the vertical distribution and type of aerosol, their size distributions, the chemical nature of aerosol observed at the surface, and timing of aerosol loading. A detailed synoptic analysis placed these observations into their transport and source-region context. Evidence suggests four major aerosol loading periods in the 25 March-30 April 2008 timeframe: a period during which typical Arctic haze conditions prevailed, several days of extremely clear conditions, rapid onset of a period dominated by Asian dust with some smoke, and a period dominated by Siberian wildfire smoke. A focused case study analysis conducted on 19 April 2008 using a balloon-borne optical particle counter suggests that, on this day, the majority of the suspended particulate matter consisted of coarse mode desiccated aerosol having undergone long-range transport. Backtrack trajectory analysis suggests aged Siberian wildfire smoke. In the last week of April, concentrations gradually decreased as synoptic conditions shifted away from favoring transport to Alaska. An important result is a strong suggestion of an Asian dust incursion in mid-April that was not well identified in other ARCTAS measurements. The lidar and OPC-sonde unambiguously discern aerosols height stratification patterns indicative of long range transport. Identification of a dust component is suggested by DRUM sampler results, which indicate crustal species, and supported by synoptic and trajectory analysis, which indicates both a source-region lifting event and appropriate air-mass pathways. [ABSTRACT FROM AUTHOR]

Aerosol measurements at Barrow, Alaska during the past 30 years have identified the long range transport of pollution associated with Arctic Haze as well as ocean-derived aerosols of more local origin. Here, we focus on measurements of aerosol chemical composition to assess (1) trends in Arctic Haze aerosol and implications for source regions, (2) the interaction between pollution-derived and ocean-derived aerosols and the resulting impacts on the chemistry of the Arctic boundary layer, and (3) the response of aerosols to a changing climate. Aerosol chemical composition measured at Barrow, AK during the Arctic haze season is compared for the years 1976-1977 and 1997-2008. Based on these two data sets, concentrations of non-sea salt (nss) sulfate (SO=4 ) and non-crustal (nc) vanadium (V) have decreased by about 60% over this 30 year period. Consistency in the ratios of nss SO=4 /ncV and nc manganese (Mn)/ncV between the two data sets indicates that, although emissions have decreased in the source regions, the source regions have remained the same over this time period. The measurements from 1997-2008 indicate that, during the haze season, the nss SO=4 aerosol at Barrow is becoming less neutralized by ammonium (NH+4 ) yielding an increasing sea salt aerosol chloride (Cl-) deficit. The expected consequence is an increase in the release of Cl atoms to the atmosphere and a change in the lifetime of volatile organic compounds (VOCs) including methane. In addition, summertime concentrations of biogenically-derived methanesulfonate (MSA-) and nss SO=4 are increasing at a rate of 12 and 8% per year, respectively. Further research is required to assess the environmental factors behind the increasing concentrations of biogenic aerosol. [ABSTRACT FROM AUTHOR]