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dc.date.accessioned2016-05-19T08:50:47Z
dc.date.available2016-05-19T08:50:47Z
dc.date.created2010-01-28T18:25:43Z
dc.date.issued2009
dc.identifier.citationKvalevåg, Maria Malene Myhre, Gunnar Myhre, Cathrine Lund . Extensive reduction of surface UV radiation since 1750 in world's populated regions. Atmospheric Chemistry and Physics. 2009, 9(20), 7737-7751
dc.identifier.urihttp://hdl.handle.net/10852/50316
dc.description.abstractHuman activity influences a wide range of components that affect the surface UV radiation levels, among them ozone at high latitudes. We calculate the effect of human-induced changes in the surface erythemally weighted ultra-violet radiation (UV-E) since 1750. We compare results from a radiative transfer model to surface UV-E radiation for year 2000 derived by satellite observations (from Total Ozone Mapping Spectroradiometer) and to ground based measurements at 14 sites. The model correlates well with the observations; the correlation coefficients are 0.97 and 0.98 for satellite and ground based measurements, respectively. In addition to the effect of changes in ozone, we also investigate the effect of changes in SO2, NO2, the direct and indirect effects of aerosols, albedo changes and aviation-induced contrails and cirrus. The results show an increase of surface UV-E in polar regions, most strongly in the Southern Hemisphere. Furthermore, our study also shows an extensive surface UV-E reduction over most land areas; a reduction up to 20% since 1750 is found in some industrialized regions. This reduction in UV-E over the industrial period is particularly large in highly populated regions.en_US
dc.languageEN
dc.language.isoenen_US
dc.publisherCopernicus
dc.rightsAttribution 3.0 Unported
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/
dc.titleExtensive reduction of surface UV radiation since 1750 in world's populated regionsen_US
dc.typeJournal articleen_US
dc.creator.authorKvalevåg, Maria Malene
dc.creator.authorMyhre, Gunnar
dc.creator.authorMyhre, Cathrine Lund
cristin.unitcode185,15,22,0
cristin.unitnameInstitutt for geofag
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode1
dc.identifier.cristin341722
dc.identifier.bibliographiccitationinfo:ofi/fmt:kev:mtx:ctx&ctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=Atmospheric Chemistry and Physics&rft.volume=9&rft.spage=7737&rft.date=2009
dc.identifier.jtitleAtmospheric Chemistry and Physics
dc.identifier.volume9
dc.identifier.issue20
dc.identifier.startpage7737
dc.identifier.endpage7751
dc.identifier.doihttp://dx.doi.org/10.5194/acp-9-7737-2009
dc.identifier.urnURN:NBN:no-53947
dc.type.documentTidsskriftartikkelen_US
dc.type.peerreviewedPeer reviewed
dc.source.issn1680-7316
dc.identifier.fulltextFulltext https://www.duo.uio.no/bitstream/handle/10852/50316/1/acp-9-7737-2009.pdf
dc.type.versionPublishedVersion


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