Particulate sulfur in the upper troposphere and lowermost stratosphere - Sources and climate forcing

dc.bibliographicCitation.firstPage10937
dc.bibliographicCitation.issue18
dc.bibliographicCitation.lastPage10953
dc.bibliographicCitation.volume17
dc.contributor.authorMartinsson, Bengt G.
dc.contributor.authorFriberg, Johan
dc.contributor.authorSandvik, Oscar S.
dc.contributor.authorHermann, Markus
dc.contributor.authorvan Velthoven, Peter F. J.
dc.contributor.authorZahn, Andreas
dc.date.accessioned2023-04-27T06:45:27Z
dc.date.available2023-04-27T06:45:27Z
dc.date.issued2017
dc.description.abstractThis study is based on fine-mode aerosol samples collected in the upper troposphere (UT) and the lowermost stratosphere (LMS) of the Northern Hemisphere extratropics during monthly intercontinental flights at 8.8-12 km altitude of the IAGOS-CARIBIC platform in the time period 1999-2014. The samples were analyzed for a large number of chemical elements using the accelerator-based methods PIXE (particle-induced X-ray emission) and PESA (particle elastic scattering analysis). Here the particulate sulfur concentrations, obtained by PIXE analysis, are investigated. In addition, the satellite-borne lidar aboard CALIPSO is used to study the stratospheric aerosol load. A steep gradient in particulate sulfur concentration extends several kilometers into the LMS, as a result of increasing dilution towards the tropopause of stratospheric, particulate sulfur-rich air. The stratospheric air is diluted with tropospheric air, forming the extratropical transition layer (ExTL). Observed concentrations are related to the distance to the dynamical tropopause. A linear regression methodology handled seasonal variation and impact from volcanism. This was used to convert each data point into stand-alone estimates of a concentration profile and column concentration of particulate sulfur in a 3 km altitude band above the tropopause. We find distinct responses to volcanic eruptions, and that this layer in the LMS has a significant contribution to the stratospheric aerosol optical depth and thus to its radiative forcing. Further, the origin of UT particulate sulfur shows strong seasonal variation. We find that tropospheric sources dominate during the fall as a result of downward transport of the Asian tropopause aerosol layer (ATAL) formed in the Asian monsoon, whereas transport down from the Junge layer is the main source of UT particulate sulfur in the first half of the year. In this latter part of the year, the stratosphere is the clearly dominating source of particulate sulfur in the UT during times of volcanic influence and under background conditions.eng
dc.description.versionpublishedVersioneng
dc.identifier.urihttps://oa.tib.eu/renate/handle/123456789/12061
dc.identifier.urihttp://dx.doi.org/10.34657/11095
dc.language.isoeng
dc.publisherKatlenburg-Lindau : EGU
dc.relation.doihttps://doi.org/10.5194/acp-17-10937-2017
dc.relation.essn1680-7324
dc.relation.ispartofseriesAtmospheric Chemistry and Physics 17 (2017), Nr. 18eng
dc.rights.licenseCC BY 3.0 Unported
dc.rights.urihttps://creativecommons.org/licenses/by/3.0
dc.subjectaerosoleng
dc.subjectCALIPSOeng
dc.subjectclimate forcingeng
dc.subjectoptical deptheng
dc.subjectparticulate mattereng
dc.subjectpollutant sourceeng
dc.subjectstratosphereeng
dc.subjectsulfureng
dc.subjecttroposphereeng
dc.subject.ddc550
dc.titleParticulate sulfur in the upper troposphere and lowermost stratosphere - Sources and climate forcingeng
dc.typearticle
dc.typeText
dcterms.bibliographicCitation.journalTitleAtmospheric Chemistry and Physics
tib.accessRightsopenAccess
wgl.contributorTROPOS
wgl.subjectGeowissenschaftenger
wgl.typeZeitschriftenartikelger
Files
Original bundle
Now showing 1 - 1 of 1
Loading...
Thumbnail Image
Name:
acp-17-10937-2017.pdf
Size:
9.23 MB
Format:
Adobe Portable Document Format
Description: