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  • Title: The effect of sources and air mass transport on the variability of trace element deposition in central Poland: a cluster-based approach.
    Author: Siudek P, Frankowski M.
    Journal: Environ Sci Pollut Res Int; 2017 Oct; 24(29):23026-23038. PubMed ID: 28822040.
    Abstract:
    Measurements of trace element (As, Cu, Cd, Cr, Ni, Pb, Zn) deposition fluxes were conducted simultaneously in two contrasted environments, i.e., urban and forest, between April 2013 and October 2014. This was the first such project in central Poland, aimed at long-term observations of trace elements in the atmosphere and their distribution, transport, and deposition pattern. The receptor sites were different in terms of local meteorological conditions, emission potential, and distance to major anthropogenic sources. The deposition fluxes of all trace elements showed clear seasonal variations, with relatively higher values in winter than in summer. The main factors affecting interannual differences in concentrations and deposition of trace elements in central Poland were local emission from industrial and commercial sources, and changes in atmospheric conditions (wind speed and direction, boundary layer, precipitation amount, air mass origin). In this study, the impact of regional and long-range transport on trace element deposition was determined using the air back-trajectory cluster analysis. During the summertime of 2013 and 2014, the predominant SW and E advections from regional and remote anthropogenic sources in Europe were responsible for high deposition of Cd, Cr, Pb, Cu, and Zn, whereas during the wintertime of 2013/2014, we observed a significant influence of polluted air masses from southeastern regions. Based on the Pb/Zn ratio, it was found that regional sources significantly influenced the aerosol composition and rainwater chemistry within the study domain. However, the role of a long-range transport of anthropogenic pollutants was also important. In addition, a relatively small difference in the Pb/Zn ratio between both sites (urban 0.26 ± 0.18, forest 0.23 ± 0.17) may suggest (1) very similar contribution of anthropogenic sources and (2) minor importance of atmospheric transformation processes of these metals in the aqueous phase.
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