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dc.contributor.authorKarl, Matthias
dc.contributor.authorLeck, Caroline
dc.contributor.authorGross, Allan
dc.contributor.authorPirjola, Liisa
dc.date.accessioned2020-04-14T12:30:26Z
dc.date.available2020-04-14T12:30:26Z
dc.date.created2012-06-01T12:53:01Z
dc.date.issued2012
dc.identifier.citationTellus. Series B, Chemical and physical meteorology. 2012, 64 .en_US
dc.identifier.issn0280-6509
dc.identifier.urihttps://hdl.handle.net/11250/2650999
dc.description.abstractEnhancement of number concentrations of particles with sizes less than 25 nm diameter has been frequently observed in the boundary layer over the central Arctic Ocean during summer. The sectional aerosol dynamics model for Marine Aerosol Formation (MAFOR) was applied to evaluate the capability of different nucleation mechanisms to reproduce nucleation events observed during three expeditions (1996, 2001 and 2008) onboard the Swedish icebreaker Oden. Model calculations suggest that a source rate of a condensable organic vapour (OV) of about 2×105 cm−3 s−1 is required to reproduce observed growth of nucleation mode particles. Nucleation rates predicted by the newly proposed combined sulphuric acid nucleation mechanism, which best described new particle formation in the Arctic, ranged from 0.04 to 0.1 cm−3 s−1. This mechanism additively combines ion-mediated nucleation and cluster activation, and treats condensation of OV without correction of the Kelvin effect. In several events, the simultaneous number enhancement of particles in the 20–50 nm size range remained unexplained by the nucleation mechanisms. This lends support to alternative theories such as the fragmentation of marine gels (≈200–500 nm diameter in size) by physical or chemical processes.en_US
dc.language.isoengen_US
dc.rightsNavngivelse-Ikkekommersiell 4.0 Internasjonal*
dc.rights.urihttp://creativecommons.org/licenses/by-nc/4.0/deed.no*
dc.titleA study of new particle formation in the marine boundary layer over the central Arctic Ocean using a flexible multicomponent aerosol dynamic modelen_US
dc.typePeer revieweden_US
dc.typeJournal articleen_US
dc.description.versionpublishedVersionen_US
dc.rights.holder© 2012 Matthias Karl et al.en_US
dc.source.pagenumber24en_US
dc.source.volume64en_US
dc.source.journalTellus. Series B, Chemical and physical meteorologyen_US
dc.identifier.doi10.3402/tellusb.v64i0.17158
dc.identifier.cristin927364
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode1


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Navngivelse-Ikkekommersiell 4.0 Internasjonal
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