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Norman et al. 1999
Norman, A.L., Barrie, L.A., Toom-Sauntry, D., Sirois, A., Krouse, H.R., Li, S.M. and Sharma, S. (1999). Sources of aerosol sulphate at Alert: Apportionment using stable isotopes. Journal of Geophysical Research 104: doi: 10.1029/1999JD900078. issn: 0148-0227.

From July 1993 to September 1994, seasonal variations in the sources of SO42- aerosols in the Arctic lower atmosphere at Alert, Canada, (82 ¿30'N, 62 ¿20'W) were investigated using the sulphur isotope abundance of as little as 10 μg of sulphur analyzed by combustion-flow isotope-ratio mass spectrometry. In conjunction with air mass trajectories and in parallel with measurements of aerosol composition, the sulphur isotope composition was used to discern sources of aerosol SO42-. Total SO42- is composed of sea-salt SO42-, marine biogenic, and nonmarine SO42-. From June through September the fraction of biogenic SO42- in the non-sea-salt (nss) component ranged from 0.09 to 0.40 with an average of 0.31¿0.11. Summertime nonmarine SO42- is likely anthropogenic in origin since it is isotopically indistinguishable from SO42- in the polluted winter/spring period of arctic haze 34S=+5?). In summer there was no significant difference in isotope composition of aerosol sulphate between air which recently traversed Eurasia and the Arctic Ocean and air arriving from North America. In contrast to summer and late winter/spring, Δ34S values for nonmarine SO42- in fall and early winter were often less than +5?. These isotopically light samples were divisible into two groups: (1) those associated with air mass trajectories potentially affected by North American soils and/or smelters and (2) three weekly samples between October and December which could be attributed to fractionated sea-salt aerosol formed on refrozen Arctic Ocean leads. For the latter the ratio of SO42-/Na was estimated to be a factor of 3.6 lower than in bulk seawater. From November to May, nonmarine aerosol SO42- was apportioned into 10 aerosol components using positive matrix factor analysis of 18 aerosol ions and trace elements <Sirois and Barrie, this issue>. In turn, a multiple linear regression of Δ34S values against the scores of the components was used to predict the isotope composition of six components. It was concluded that the main mass of anthropogenic SO42- had a Δ34S value near +5? and that biogenic SO42- had a Δ34S of +16¿3.9?. Reasonable agreement between model results and sulphur isotope measurements at Alert show that SO42- apportionment using positive matrix factor analysis is a reasonable approach which gives realistic results. ¿ 1999 American Geophysical Union

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Abstract

Keywords
Atmospheric Composition and Structure, Aerosols and particles (0345, 4801), Atmospheric Composition and Structure, Constituent sources and sinks, Atmospheric Composition and Structure, Pollution—urban and regional, Atmospheric Composition and Structure, Troposphere—composition and chemistry, Atmospheric Composition and Structure, Cloud physics and chemistry, Meteorology and Atmospheric Dynamics, Polar meteorology, Meteorology and Atmospheric Dynamics, Precipitation
Journal
Journal of Geophysical Research
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Publisher
American Geophysical Union
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