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dc.date.accessioned2015-02-04T14:50:22Z
dc.date.available2015-02-04T14:50:22Z
dc.date.created2014-08-22T11:26:16Z
dc.date.issued2014
dc.identifier.citationIsaksen, Ivar S A Berntsen, Terje Koren Dalsøren, Stig Bjørløw Eleftheratos, K. Orsolini, Yvan Rognerud, Bjørg Stordal, Frode Søvde, Ole Amund Zerefos, C Holmes, Chris D. . Atmospheric Ozone and Methane in a Changing Climate. Atmosphere. 2014, 5(3), 518-535
dc.identifier.urihttp://hdl.handle.net/10852/42026
dc.description.abstractOzone and methane are chemically active climate-forcing agents affected by climate–chemistry interactions in the atmosphere. Key chemical reactions and processes affecting ozone and methane are presented. It is shown that climate-chemistry interactions have a significant impact on the two compounds. Ozone, which is a secondary compound in the atmosphere, produced and broken down mainly in the troposphere and stratosphre through chemical reactions involving atomic oxygen (O), NOx compounds (NO, NO2), CO, hydrogen radicals (OH, HO2), volatile organic compounds (VOC) and chlorine (Cl, ClO) and bromine (Br, BrO). Ozone is broken down through changes in the atmospheric distribution of the afore mentioned compounds. Methane is a primary compound emitted from different sources (wetlands, rice production, livestock, mining, oil and gas production and landfills).Methane is broken down by the hydroxyl radical (OH). OH is significantly affected by methane emissions, defined by the feedback factor, currently estimated to be in the range 1.3 to 1.5, and increasing with increasing methane emission. Ozone and methane changes are affected by NOx emissions. While ozone in general increase with increases in NOx emission, methane is reduced, due to increases in OH. Several processes where current and future changes have implications for climate-chemistry interactions are identified. It is also shown that climatic changes through dynamic processes could have significant impact on the atmospheric chemical distribution of ozone and methane, as we can see through the impact of Quasi Biennial Oscillation (QBO). Modeling studies indicate that increases in ozone could be more pronounced toward the end of this century. Thawing permafrost could lead to important positive feedbacks in the climate system. Large amounts of organic material are stored in the upper layers of the permafrost in the yedoma deposits in Siberia, where 2 to 5% of the deposits could be organic material. During thawing of permafrost, parts of the organic material that is deposited could be converted to methane. Furthermore, methane stored in deposits under shallow waters in the Arctic have the potential to be released in a future warmer climate with enhanced climate impact on methane, ozone and stratospheric water vapor. Studies performed by several groups show that the transport sectors have the potential for significant impacts on climate-chemistry interactions. There are large uncertainties connected to ozone and methane changes from the transport sector, and to methane release and climate impact during permafrost thawing.en_US
dc.languageEN
dc.language.isoenen_US
dc.publisherMultidisciplinary Digital Publishing Institute (MDPI)
dc.rightsAttribution 3.0 Unported
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/
dc.titleAtmospheric Ozone and Methane in a Changing Climateen_US
dc.typeJournal articleen_US
dc.creator.authorIsaksen, Ivar S A
dc.creator.authorBerntsen, Terje Koren
dc.creator.authorDalsøren, Stig Bjørløw
dc.creator.authorEleftheratos, K.
dc.creator.authorOrsolini, Yvan
dc.creator.authorRognerud, Bjørg
dc.creator.authorStordal, Frode
dc.creator.authorSøvde, Ole Amund
dc.creator.authorZerefos, C
dc.creator.authorHolmes, Chris D.
cristin.unitcode185,15,22,0
cristin.unitnameInstitutt for geofag
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode1
dc.identifier.cristin1148727
dc.identifier.bibliographiccitationinfo:ofi/fmt:kev:mtx:ctx&ctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=Atmosphere&rft.volume=5&rft.spage=518&rft.date=2014
dc.identifier.jtitleAtmosphere
dc.identifier.volume5
dc.identifier.issue3
dc.identifier.startpage518
dc.identifier.endpage535
dc.identifier.doihttp://dx.doi.org/10.3390/atmos5030518
dc.identifier.urnURN:NBN:no-46432
dc.type.documentTidsskriftartikkelen_US
dc.type.peerreviewedPeer reviewed
dc.source.issn2073-4433
dc.identifier.fulltextFulltext https://www.duo.uio.no/bitstream/handle/10852/42026/2/atmosphere-05-00518.pdf
dc.type.versionPublishedVersion


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