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European Geosciences Union, Atmospheric Chemistry and Physics Discussions, 10(14), p. 15591-15643

DOI: 10.5194/acpd-14-15591-2014

European Geosciences Union, Atmospheric Chemistry and Physics, 24(14), p. 13551-13570, 2014

DOI: 10.5194/acp-14-13551-2014

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Radiocarbon analysis of elemental and organic carbon in Switzerland during winter-smog episodes from 2008 to 2012 – Part 1: Source apportionment and spatial variability

This paper is made freely available by the publisher.
This paper is made freely available by the publisher.

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Abstract

While several studies have investigated winter-time air pollution with a wide range of concentration levels, hardly any results are available for longer time periods covering several winter-smog episodes at various locations; e.g., often only a few weeks from a single winter are investigated. Here, we present source apportionment results of winter-smog episodes from 16 air pollution monitoring stations across Switzerland from five consecutive winters. Radiocarbon ( 14 C) analyses of the elemental (EC) and organic (OC) carbon fractions, as well as levoglucosan, major water-soluble ionic species and gas-phase pollutant measurements were used to characterize the different sources of PM 10 . The most important contributions to PM 10 during winter-smog episodes in Switzerland were on average the secondary inorganic constituents (sum of nitrate, sulfate and ammonium = 41 ± 15%) followed by organic matter (OM) (34 ± 13%) and EC (5 ± 2%). The non-fossil fractions of OC ( f NF,OC ) ranged on average from 69 to 85 and 80 to 95% for stations north and south of the Alps, respectively, showing that traffic contributes on average only up to ~ 30% to OC. The non-fossil fraction of EC ( f NF,EC ), entirely attributable to primary wood burning, was on average 42 ± 13 and 49 ± 15% for north and south of the Alps, respectively. While a high correlation was observed between fossil EC and nitrogen oxides, both primarily emitted by traffic, these species did not significantly correlate with fossil OC (OC F ), which seems to suggest that a considerable amount of OC F is secondary, from fossil precursors. Elevated f NF,EC and f NF,OC values and the high correlation of the latter with other wood burning markers, including levoglucosan and water soluble potassium (K + ) indicate that residential wood burning is the major source of carbonaceous aerosols during winter-smog episodes in Switzerland. The inspection of the non-fossil OC and EC levels and the relation with levoglucosan and water-soluble K + shows different ratios for stations north and south of the Alps (most likely because of differences in burning technologies) for these two regions in Switzerland.