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dc.contributor.authorChang, R. Y. -Wen_US
dc.contributor.authorLeck, C.en_US
dc.contributor.authorGraus, M.en_US
dc.contributor.authorMueller, M.en_US
dc.contributor.authorPaatero, J.en_US
dc.contributor.authorBurkhart, J. F.en_US
dc.contributor.authorStohl, A.en_US
dc.contributor.authorOrr, L. H.en_US
dc.contributor.authorHayden, K.en_US
dc.contributor.authorLi, S. -Men_US
dc.contributor.authorHansel, A.en_US
dc.contributor.authorTjernstrom, M.en_US
dc.contributor.authorLeaitch, W. R.en_US
dc.contributor.authorAbbatt, J. P. D.en_US
dc.date.accessioned2014-02-24T16:50:08Z
dc.date.available2014-02-24T16:50:08Z
dc.date.issued2011en_US
dc.identifier.citationChang, R. Y. -W, C. Leck, M. Graus, M. Mueller, et al. 2011. "Aerosol composition and sources in the central Arctic Ocean during ASCOS." Atmospheric Chemistry and Physics 11(20): 10619-10636.en_US
dc.identifier.issn1680-7316en_US
dc.identifier.urihttp://dx.doi.org/10.5194/acp-11-10619-2011en_US
dc.identifier.urihttp://hdl.handle.net/10222/44546
dc.description.abstractMeasurements of submicron aerosol chemical composition were made over the central Arctic Ocean from 5 August to 8 September 2008 as a part of the Arctic Summer Cloud Ocean Study (ASCOS) using an aerosol mass spectrometer (AMS). The median levels of sulphate and organics for the entire study were 0.051 and 0.055 mu gm(-3), respectively. Positive matrix factorisation was performed on the entire mass spectral time series and this enabled marine biogenic and continental sources of particles to be separated. These factors accounted for 33% and 36% of the sampled ambient aerosol mass, respectively, and they were both predominantly composed of sulphate, with 47% of the sulphate apportioned to marine biogenic sources and 48% to continental sources, by mass. Within the marine biogenic factor, the ratio of methane sulphonate to sulphate was 0.25+/-0.02, consistent with values reported in the literature. The organic component of the continental factor was more oxidised than that of the marine biogenic factor, suggesting that it had a longer photochemical lifetime than the organics in the marine biogenic factor. The remaining ambient aerosol mass was apportioned to an organic-rich factor that could have arisen from a combination of marine and continental sources. In particular, given that the factor does not correlate with common tracers of continental influence, we cannot rule out that the organic factor arises from a primary marine source.en_US
dc.relation.ispartofAtmospheric Chemistry and Physicsen_US
dc.titleAerosol composition and sources in the central Arctic Ocean during ASCOSen_US
dc.typearticleen_US
dc.identifier.volume11en_US
dc.identifier.issue20en_US
dc.identifier.startpage10619en_US
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