Measurements of aerosol and CCN properties in the Mackenzie River delta (Canadian Arctic) during spring-summer transition in May 2014

dc.bibliographicCitation.firstPage4477
dc.bibliographicCitation.issue7
dc.bibliographicCitation.lastPage4496
dc.bibliographicCitation.volume18
dc.contributor.authorHerenz, Paul
dc.contributor.authorWex, Heike
dc.contributor.authorHenning, Silvia
dc.contributor.authorKristensen, Thomas Bjerring
dc.contributor.authorRubach, Florian
dc.contributor.authorRoth, Anja
dc.contributor.authorBorrmann, Stephan
dc.contributor.authorBozem, Heiko
dc.contributor.authorSchulz, Hannes
dc.contributor.authorStratmann, Frank
dc.date.accessioned2023-04-27T06:45:29Z
dc.date.available2023-04-27T06:45:29Z
dc.date.issued2018
dc.description.abstractWithin the framework of the RACEPAC (Radiation-Aerosol-Cloud Experiment in the Arctic Circle) project, the Arctic aerosol, arriving at a ground-based station in Tuktoyaktuk (Mackenzie River delta area, Canada), was characterized during a period of 3 weeks in May 2014. Basic meteorological parameters and particle number size distributions (PNSDs) were observed and two distinct types of air masses were found. One type were typical Arctic haze air masses, termed accumulation-type air masses, characterized by a monomodal PNSD with a pronounced accumulation mode at sizes above 100 nm. These air masses were observed during a period when back trajectories indicate an air mass origin in the north-east of Canada. The other air mass type is characterized by a bimodal PNSD with a clear minimum around 90ĝ€†nm and with an Aitken mode consisting of freshly formed aerosol particles. Back trajectories indicate that these air masses, termed Aitken-type air masses, originated from the North Pacific. In addition, the application of the PSCF receptor model shows that air masses with their origin in active fire areas in central Canada and Siberia, in areas of industrial anthropogenic pollution (Norilsk and Prudhoe Bay Oil Field) and the north-west Pacific have enhanced total particle number concentrations (N CN). Generally, N CN ranged from 20 to 500 cmg'3, while cloud condensation nuclei (CCN) number concentrations were found to cover a range from less than 10 up to 250 cmg'3 for a supersaturation (SS) between 0.1 and 0.7 %. The hygroscopicity parameter of the CCN was determined to be 0.23 on average and variations in were largely attributed to measurement uncertainties. <br><br> Furthermore, simultaneous PNSD measurements at the ground station and on the Polar 6 research aircraft were performed. We found a good agreement of ground-based PNSDs with those measured between 200 and 1200 m. During two of the four overflights, particle number concentrations at 3000 m were found to be up to 20 times higher than those measured below 2000 m; for one of these two flights, PNSDs measured above 2000 m showed a different shape than those measured at lower altitudes. This is indicative of long-range transport from lower latitudes into the Arctic that can advect aerosol from different regions in different heights.eng
dc.description.versionpublishedVersioneng
dc.identifier.urihttps://oa.tib.eu/renate/handle/123456789/12082
dc.identifier.urihttp://dx.doi.org/10.34657/11116
dc.language.isoeng
dc.publisherKatlenburg-Lindau : EGU
dc.relation.doihttps://doi.org/10.5194/acp-18-4477-2018
dc.relation.essn1680-7324
dc.relation.ispartofseriesAtmospheric Chemistry and Physics 18 (2018), Nr. 7eng
dc.rights.licenseCC BY 4.0 Unported
dc.rights.urihttps://creativecommons.org/licenses/by/4.0
dc.subjectaerosoleng
dc.subjectair masseng
dc.subjectcloud condensation nucleuseng
dc.subjectconcentration (composition)eng
dc.subjectlong range transporteng
dc.subjectparticle sizeeng
dc.subjectseasonal variationeng
dc.subjectsize distributioneng
dc.subjectCanadaeng
dc.subjectCanadian Arcticeng
dc.subjectMackenzie Deltaeng
dc.subjectNorthwest Territorieseng
dc.subjectSiberiaeng
dc.subjectTuktoyaktukeng
dc.subject.ddc550
dc.titleMeasurements of aerosol and CCN properties in the Mackenzie River delta (Canadian Arctic) during spring-summer transition in May 2014eng
dc.typearticle
dc.typeText
dcterms.bibliographicCitation.journalTitleAtmospheric Chemistry and Physics
tib.accessRightsopenAccess
wgl.contributorTROPOS
wgl.subjectGeowissenschaftenger
wgl.typeZeitschriftenartikelger
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