Author:
Chalbot M.-C.,McElroy B.,Kavouras I. G.
Abstract
Abstract. The sources of fine particles over a 10 yr period at Little Rock, Arkansas, an urban area in southern Mississippi Valley, were identified by positive matrix factorization. The annual trends of PM2.5 and its sources and their associations with the pathways of air mass backward trajectories were examined. Seven sources were apportioned, namely, primary traffic particles, secondary nitrate and sulphate, biomass burning, diesel particles, aged/contaminated sea salt and mineral/road dust, accounting for more than 90% of measured PM2.5 mass. The declining trend of PM2.5 mass (0.4 μg m−3 yr−1) was related to lower levels of SO42− (0.2 μg m−3 yr−1) due to SO2 reductions from point and mobile sources. The slower decline for NO3− particles (0.1 μg m−3 yr−1) was attributed to the spatial variability of NH3 in Midwest. The annual variation of biomass burning particles was associated with wildland fires in southeast and northwest US that are sensitive to climate changes. The four regions within 500 km from the receptor site, the Gulf Coast and southeast US accounted cumulatively for more than 65% of PM2.5 mass, nitrate, sulphate and biomass burning aerosol. Overall, more than 50% of PM2.5 and its sources originated from sources outside the state. Sources within the Gulf Coast and western Gulf of Mexico include 65% of the busiest ports in the US, intense marine traffic within 400 km of the coast burning rich in S diesel, and a large number of offshore oil and natural gas platforms and many refineries along the coast. This approach allowed for quantitatively assessing the impacts of transport from regions representing diverse mixtures of sources and weather conditions for different types of particles. The findings of this effort demonstrated the influences of emission controls on SO2 and NOx on PM2.5 mass, the potential effect of events (i.e. fires) sensitive to climate change phenomena on air pollution and the potential of offshore activities and shipping emissions to influence air quality in urban areas located more than 1000 km away from the sources.
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