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dc.date.accessioned2016-05-20T10:49:54Z
dc.date.available2016-05-20T10:49:54Z
dc.date.created2012-11-26T13:42:02Z
dc.date.issued2012
dc.identifier.citationHodnebrog, Øivind Solberg, Sverre Stordal, Frode Svendby, Tove Marit Simpson, David Gauss, Michael Hilboll, Andreas Pfister, G. Turquety, Solène Richter, Andreas Burrows, John P. Denier van der Gon, H. A. C. . Impact of forest fires, biogenic emissions and high temperatures on the elevated Eastern Meditteranean ozone levels during the hot summer of 2007. Atmospheric Chemistry and Physics. 2012, 12(18), 8727-8750
dc.identifier.urihttp://hdl.handle.net/10852/50327
dc.description.abstractThe hot summer of 2007 in southeast Europe has been studied using two regional atmospheric chemistry models; WRF-Chem and EMEP MSC-W. The region was struck by three heat waves and a number of forest fire episodes, greatly affecting air pollution levels. We have focused on ozone and its precursors using state-of-the-art inventories for anthropogenic, biogenic and forest fire emissions. The models have been evaluated against measurement data, and processes leading to ozone formation have been quantified. Heat wave episodes are projected to occur more frequently in a future climate, and therefore this study also makes a contribution to climate change impact research. The plume from the Greek forest fires in August 2007 is clearly seen in satellite observations of CO and NO2 columns, showing extreme levels of CO in and downwind of the fires. Model simulations reflect the location and influence of the fires relatively well, but the modelled magnitude of CO in the plume core is too low. Most likely, this is caused by underestimation of CO in the emission inventories, suggesting that the CO/NOx ratios of fire emissions should be re-assessed. Moreover, higher maximum values are seen in WRF-Chem than in EMEP MSC-W, presumably due to differences in plume rise altitudes as the first model emits a larger fraction of the fire emissions in the lowermost model layer. The model results are also in fairly good agreement with surface ozone measurements. Biogenic VOC emissions reacting with anthropogenic NOx emissions are calculated to contribute significantly to the levels of ozone in the region, but the magnitude and geographical distribution depend strongly on the model and biogenic emission module used. During the July and August heat waves, ozone levels increased substantially due to a combination of forest fire emissions and the effect of high temperatures. We found that the largest temperature impact on ozone was through the temperature dependence of the biogenic emissions, closely followed by the effect of reduced dry deposition caused by closing of the plants’ stomata at very high temperatures. The impact of high temperatures on the ozone chemistry was much lower. The results suggest that forest fire emissions, and the temperature effect on biogenic emissions and dry deposition, will potentially lead to substantial ozone increases in a warmer climate.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.titleImpact of forest fires, biogenic emissions and high temperatures on the elevated Eastern Meditteranean ozone levels during the hot summer of 2007en_US
dc.typeJournal articleen_US
dc.creator.authorHodnebrog, Øivind
dc.creator.authorSolberg, Sverre
dc.creator.authorStordal, Frode
dc.creator.authorSvendby, Tove Marit
dc.creator.authorSimpson, David
dc.creator.authorGauss, Michael
dc.creator.authorHilboll, Andreas
dc.creator.authorPfister, G.
dc.creator.authorTurquety, Solène
dc.creator.authorRichter, Andreas
dc.creator.authorBurrows, John P.
dc.creator.authorDenier van der Gon, H. A. C.
cristin.unitcode185,15,22,0
cristin.unitnameInstitutt for geofag
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.fulltextoriginal
cristin.qualitycode1
dc.identifier.cristin965009
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=12&rft.spage=8727&rft.date=2012
dc.identifier.jtitleAtmospheric Chemistry and Physics
dc.identifier.volume12
dc.identifier.issue18
dc.identifier.startpage8727
dc.identifier.endpage8750
dc.identifier.doihttp://dx.doi.org/10.5194/acp-12-8727-2012
dc.identifier.urnURN:NBN:no-53960
dc.type.documentTidsskriftartikkelen_US
dc.type.peerreviewedPeer reviewed
dc.source.issn1680-7316
dc.identifier.fulltextFulltext https://www.duo.uio.no/bitstream/handle/10852/50327/1/acp-12-8727-2012.pdf
dc.identifier.fulltextFulltext https://www.duo.uio.no/bitstream/handle/10852/50327/2/suppl-acp-12-8727-2012.pdf
dc.type.versionPublishedVersion


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