Skjul metadata

dc.date.accessioned2020-05-25T18:47:23Z
dc.date.available2020-05-25T18:47:23Z
dc.date.created2019-06-19T13:01:49Z
dc.date.issued2019
dc.identifier.citationSporre, Moa Kristina Blichner, Sara Marie Karset, Inger Helene H. Makkonen, Risto Berntsen, Terje Koren . BVOC-aerosol-climate feedbacks investigated using NorESM. Atmospheric Chemistry and Physics. 2019, 19(7), 4763-4782
dc.identifier.urihttp://hdl.handle.net/10852/76240
dc.description.abstractBoth higher temperatures and increased CO2 concentrations are (separately) expected to increase the emissions of biogenic volatile organic compounds (BVOCs). This has been proposed to initiate negative climate feedback mechanisms through increased formation of secondary organic aerosol (SOA). More SOA can make the clouds more reflective, which can provide a cooling. Furthermore, the increase in SOA formation has also been proposed to lead to increased aerosol scattering, resulting in an increase in diffuse radiation. This could boost gross primary production (GPP) and further increase BVOC emissions. In this study, we have used the Norwegian Earth System Model (NorESM) to investigate both these feedback mechanisms. Three sets of experiments were set up to quantify the feedback with respect to (1) doubling the CO2, (2) increasing temperatures corresponding to a doubling of CO2 and (3) the combined effect of both doubling CO2 and a warmer climate. For each of these experiments, we ran two simulations, with identical setups, except for the BVOC emissions. One simulation was run with interactive BVOC emissions, allowing the BVOC emissions to respond to changes in CO2 and/or climate. In the other simulation, the BVOC emissions were fixed at present-day conditions, essentially turning the feedback off. The comparison of these two simulations enables us to investigate each step along the feedback as well as estimate their overall relevance for the future climate. We find that the BVOC feedback can have a significant impact on the climate. The annual global BVOC emissions are up to 63 % higher when the feedback is turned on compared to when the feedback is turned off, with the largest response when both CO2 and climate are changed. The higher BVOC levels lead to the formation of more SOA mass (max 53 %) and result in more particles through increased new particle formation as well as larger particles through increased condensation. The corresponding changes in the cloud properties lead to a −0.43 W m−2 stronger net cloud forcing. This effect becomes about 50 % stronger when the model is run with reduced anthropogenic aerosol emissions, indicating that the feedback will become even more important as we decrease aerosol and precursor emissions. We do not find a boost in GPP due to increased aerosol scattering on a global scale. Instead, the fate of the GPP seems to be controlled by the BVOC effects on the clouds. However, the higher aerosol scattering associated with the higher BVOC emissions is found to also contribute with a potentially important enhanced negative direct forcing (−0.06 W m−2). The global total aerosol forcing associated with the feedback is −0.49 W m−2, indicating that it has the potential to offset about 13 % of the forcing associated with a doubling of CO2.en_US
dc.languageEN
dc.publisherCopernicus GmbH
dc.rightsAttribution 4.0 International
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.titleBVOC-aerosol-climate feedbacks investigated using NorESMen_US
dc.typeJournal articleen_US
dc.creator.authorSporre, Moa Kristina
dc.creator.authorBlichner, Sara Marie
dc.creator.authorKarset, Inger Helene H.
dc.creator.authorMakkonen, Risto
dc.creator.authorBerntsen, Terje Koren
cristin.unitcode185,15,22,0
cristin.unitnameInstitutt for geofag
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode2
dc.identifier.cristin1706073
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=19&rft.spage=4763&rft.date=2019
dc.identifier.jtitleAtmospheric Chemistry and Physics
dc.identifier.volume19
dc.identifier.issue7
dc.identifier.startpage4763
dc.identifier.endpage4782
dc.identifier.doihttps://doi.org/10.5194/acp-19-4763-2019
dc.identifier.urnURN:NBN:no-79368
dc.type.documentTidsskriftartikkelen_US
dc.type.peerreviewedPeer reviewed
dc.source.issn1680-7316
dc.identifier.fulltextFulltext https://www.duo.uio.no/bitstream/handle/10852/76240/1/acp-19-4763-2019.pdf
dc.type.versionPublishedVersion


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