Presented here are results obtained from national and international deployments of the Aerodyne Aerosol Mass Spectrometer (AMS) system by different research groups. The AMS is capable of providing size and compositionally resolved mass loadings of non-refractory aerosol components in real time. Recent deployments of the AMS include field campaigns in Houston (TEXAQS 2000), New York City (PMTACS 2001), Michigan (PROPHET 2001), Vancouver (PACIFIC 2001), Pittsburg (PAQS 2002), New England (NEAQS 2002), and Mexico City (2002 and 2003). An analysis of aerosol mass, size, and composition trends obtained during these campaigns reveal diurnal variations in the photochemically driven formation of sulfate, nitrate, and oxidized organic aerosols. The chemical composition of these aerosols can be clearly distinguished from those observed during vehicular exhaust or biomass burning pollution events. These results, when combined with airmass backtrajectory calculations and ancillary gas phase measurements allow for the characterization of particle sources. Similarities and differences in aerosol size and chemical composition as well as aerosol formation and transformation at these widely varying sampling locations will be discussed.
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