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dc.contributor.authorLeibensperger, Eric Michael
dc.contributor.authorMickley, L. J.
dc.contributor.authorChen, W. -T.
dc.contributor.authorSeinfeld, J. H.
dc.contributor.authorNenes, A.
dc.contributor.authorAdams, P. J.
dc.contributor.authorStreets, D. G.
dc.contributor.authorKumar, N.
dc.contributor.authorRind, D.
dc.date.accessioned2012-10-18T17:53:08Z
dc.date.available2012-10-18T17:53:08Z
dc.date.issued2012-04
dc.date.submitted2011-12
dc.identifier.issn1680-7375
dc.identifier.issn1680-7367
dc.identifier.urihttp://hdl.handle.net/1721.1/74090
dc.description.abstractWe investigate the climate response to changing US anthropogenic aerosol sources over the 1950–2050 period by using the NASA GISS general circulation model (GCM) and comparing to observed US temperature trends. Time-dependent aerosol distributions are generated from the GEOS-Chem chemical transport model applied to historical emission inventories and future projections. Radiative forcing from US anthropogenic aerosols peaked in 1970–1990 and has strongly declined since due to air quality regulations. We find that the regional radiative forcing from US anthropogenic aerosols elicits a strong regional climate response, cooling the central and eastern US by 0.5–1.0 °C on average during 1970–1990, with the strongest effects on maximum daytime temperatures in summer and autumn. Aerosol cooling reflects comparable contributions from direct and indirect (cloud-mediated) radiative effects. Absorbing aerosol (mainly black carbon) has negligible warming effect. Aerosol cooling reduces surface evaporation and thus decreases precipitation along the US east coast, but also increases the southerly flow of moisture from the Gulf of Mexico resulting in increased cloud cover and precipitation in the central US. Observations over the eastern US show a lack of warming in 1960–1980 followed by very rapid warming since, which we reproduce in the GCM and attribute to trends in US anthropogenic aerosol sources. Present US aerosol concentrations are sufficiently low that future air quality improvements are projected to cause little further warming in the US (0.1 °C over 2010–2050). We find that most of the warming from aerosol source controls in the US has already been realized over the 1980–2010 period.en_US
dc.language.isoen_US
dc.publisherCopernicus GmbHen_US
dc.relation.isversionofhttp://dx.doi.org/10.5194/acp-12-3349-2012en_US
dc.rightsCreative Commons Attribution 3.0en_US
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/en_US
dc.sourceCopernicusen_US
dc.titleClimatic effects of 1950–2050 changes in US anthropogenic aerosols – Part 2: Climate responseen_US
dc.typeArticleen_US
dc.identifier.citationLeibensperger, E. M. et al. “Climatic Effects of 1950-2050 Changes in US Anthropogenic Aerosols -Part 2: Climate Response.” Atmospheric Chemistry and Physics 12.7 (2012): 3349–3362.en_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Earth, Atmospheric, and Planetary Sciencesen_US
dc.contributor.mitauthorLeibensperger, Eric Michael
dc.relation.journalAtmospheric Chemistry and Physics Discussionsen_US
dc.eprint.versionFinal published versionen_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dspace.orderedauthorsLeibensperger, E. M.; Mickley, L. J.; Jacob, D. J.; Chen, W.-T.; Seinfeld, J. H.; Nenes, A.; Adams, P. J.; Streets, D. G.; Kumar, N.; Rind, D.en
mit.licensePUBLISHER_CCen_US
mit.metadata.statusComplete


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