Cloud condensation nuclei spectra derived from size distributions and hygroscopic properties of the aerosol in coastal south-west Portugal during ACE-2

dc.bibliographicCitation.firstPage35
dc.bibliographicCitation.issue1eng
dc.bibliographicCitation.lastPage53
dc.bibliographicCitation.volume55
dc.contributor.authorDusek, Ulrike
dc.contributor.authorCovert, David S.
dc.contributor.authorWiedensohler, Alfred
dc.contributor.authorNeusüss, Christian
dc.contributor.authorWeise, Diana
dc.contributor.authorCantrell, Will
dc.date.accessioned2018-02-09T04:39:45Z
dc.date.available2019-06-26T17:17:26Z
dc.date.issued2016
dc.description.abstractIn this work we propose and test a method to calculate cloud condensation nuclei (CCN) spectra basedon aerosol number size distributions and hygroscopic growth factors. Sensitivity studies show thatthis method can be used in a wide variety of conditions except when the aerosol consist mainly oforganic compounds. One crucial step in the calculations, estimating soluble ions in an aerosol particlebased on hygroscopic growth factors, is tested in an internal hygroscopic consistency study. The resultsshow that during the second Aerosol Characterization Experiment (ACE-2) the number concentrationof inorganic ions analyzed in impactor samples could be reproduced from measured growth factorswithin the measurement uncertainties at the measurement site in Sagres, Portugal. CCN spectra were calculated based on data from the ACE-2 field experiment at the Sagres site.The calculations overestimate measured CCN spectra on average by approximately 30%, which iscomparable to the uncertainties in measurements and calculations at supersaturations below 0.5%. Thecalculated CCN spectra were averaged over time periods when Sagres received clean air masses and airmasses influenced by aged and recent pollution. Pollution outbreaks enhance the CCN concentrationsat supersaturations near 0.2% by a factor of 3 (aged pollution) to 5 (recent pollution) compared to theclean marine background concentrations. In polluted air masses, the shape of the CCN spectra changes.The clean spectra can be approximated by a power function, whereas the polluted spectra are betterapproximated by an error function.eng
dc.description.versionpublishedVersioneng
dc.formatapplication/pdf
dc.identifier.urihttps://doi.org/10.34657/859
dc.identifier.urihttps://oa.tib.eu/renate/handle/123456789/392
dc.language.isoengeng
dc.publisherMilton Park : Taylor & Franciseng
dc.relation.doihttps://doi.org/10.3402/tellusb.v55i1.16357
dc.relation.ispartofseriesTellus B: Chemical and Physical Meteorology, Volume 55, Issue 1, Page 35-53eng
dc.rights.licenseCC BY 4.0 Unportedeng
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/eng
dc.subjectaerosol propertyeng
dc.subjectatmospheric pollutioneng
dc.subjectcloud condensation nucleuseng
dc.subjecthygroscopicityeng
dc.subjectsize distributioneng
dc.subject.ddc550eng
dc.titleCloud condensation nuclei spectra derived from size distributions and hygroscopic properties of the aerosol in coastal south-west Portugal during ACE-2eng
dc.typearticleeng
dc.typeTexteng
dcterms.bibliographicCitation.journalTitleTellus B: Chemical and Physical Meteorologyeng
tib.accessRightsopenAccesseng
wgl.contributorTROPOSeng
wgl.subjectGeowissenschafteneng
wgl.typeZeitschriftenartikeleng
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