Occurrence of an ultrafine particle mode less than 20 nm in diameter in the marine boundary layer during Arctic summer and autumn

dc.bibliographicCitation.firstPage213
dc.bibliographicCitation.issue2eng
dc.bibliographicCitation.lastPage222
dc.bibliographicCitation.volume48
dc.contributor.authorWiedensohler, Alfred
dc.contributor.authorCovert, David S.
dc.contributor.authorSwietlicki, Erik
dc.contributor.authorAalto, Pasi
dc.contributor.authorHeintzenberg, Jost
dc.contributor.authorLeck, Caroline
dc.date.accessioned2018-02-09T16:40:07Z
dc.date.available2019-06-26T17:17:36Z
dc.date.issued2017
dc.description.abstractThe International Arctic Ocean Expedition 1991 (IAOE-91) provided a platform to study the occurrence and size distributions of ultrafine particles in the marine boundary layer (MBL) during Arctic summer and autumn. Measurements of both aerosol physics, and gas/particulate chemistry were taken aboard the Swedish icebreaker Oden. Three separate submicron aerosol modes were found: an ultrafine mode (Dp < 20 nm), the Aitken mode (20 < Dp < 100 nm), and the accumulation mode (Dp > 100 nm). We evaluated correlations between ultrafine particle number concentrations and mean diameter with the entire measured physical, chemical, and meteorological data set. Multivariate statistical methods were then used to make these comparisons. A principal component (PC) analysis indicated that the observed variation in the data could be explained by the influence from several types of air masses. These were characterised by contributions from the open sea or sources from the surrounding continents and islands. A partial least square (PLS) regression of the ultrafine particle concentration was also used. These results implied that the ultrafine particles were produced above or in upper layers of the MBL and mixed downwards. There were also indications that the open sea acted as a source of the precursors for ultrafine particle production. No anti-correlation was found between the ultrafine and accumulation particle number concentrations, thus indicating that the sources were in separate air masses.eng
dc.description.versionpublishedVersioneng
dc.formatapplication/pdf
dc.identifier.urihttps://doi.org/10.34657/1131
dc.identifier.urihttps://oa.tib.eu/renate/handle/123456789/431
dc.language.isoengeng
dc.publisherMilton Park : Taylor & Franciseng
dc.relation.doihttps://doi.org/10.3402/tellusb.v48i2.15887
dc.relation.ispartofseriesTellus B: Chemical and Physical Meteorology, Volume 48, Issue 2, Page 213-222eng
dc.rights.licenseCC BY 4.0 Unportedeng
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/eng
dc.subjectair mass typeeng
dc.subjectatmospheric particulateseng
dc.subjectIAOEeng
dc.subjectmarine boundary layereng
dc.subjectoceanic boundary layereng
dc.subjectshipborne observationeng
dc.subjectsubmicron aerosol modeeng
dc.subjectultrafine particleeng
dc.subjectultrafine particle modeeng
dc.subject.ddc550eng
dc.titleOccurrence of an ultrafine particle mode less than 20 nm in diameter in the marine boundary layer during Arctic summer and autumneng
dc.typearticleeng
dc.typeTexteng
dcterms.bibliographicCitation.journalTitleTellus B: Chemical and Physical Meteorologyeng
tib.accessRightsopenAccesseng
wgl.contributorTROPOSeng
wgl.subjectGeowissenschafteneng
wgl.typeZeitschriftenartikeleng
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