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dc.contributor.authorLeibensperger, E
dc.contributor.authorMickley, Loretta J.
dc.contributor.authorJacob, Daniel 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.accessioned2014-03-17T16:07:52Z
dc.date.issued2012
dc.identifier.citationLeibensperger, E. M., L. J. Mickley, D. J. Jacob, W.-T. Chen, J. H. Seinfeld, A. Nenes, P. J. Adams, D. G. Streets, N. Kumar, and D. Rind. 2012. Climatic Effects of 1950-2050 Changes in US Anthropogenic Aerosols - Part 1: Aerosol Trends and Radiative Forcing. Atmospheric Chemistry and Physics 12, no. 7: 3333–3348.en_US
dc.identifier.issn1680-7316en_US
dc.identifier.issn1680-7324en_US
dc.identifier.urihttp://nrs.harvard.edu/urn-3:HUL.InstRepos:11916600
dc.description.abstractWe calculate decadal aerosol direct and indirect (warm cloud) radiative forcings from US anthropogenic sources over the 1950–2050 period. Past and future aerosol distributions are constructed using GEOS-Chem and historical emission inventories and future projections from the IPCC A1B scenario. Aerosol simulations are evaluated with observed spatial distributions and 1980–2010 trends of aerosol concentrations and wet deposition in the contiguous US. Direct and indirect radiative forcing is calculated using the GISS general circulation model and monthly mean aerosol distributions from GEOS-Chem. The radiative forcing from US anthropogenic aerosols is strongly localized over the eastern US. We find that its magnitude peaked in 1970–1990, with values over the eastern US (east of 100° W) of −2.0 W m−2 for direct forcing including contributions from sulfate (−2.0 W m−2), nitrate (−0.2 W m−2), organic carbon (−0.2 W m−2), and black carbon (+0.4 W m−2). The uncertainties in radiative forcing due to aerosol radiative properties are estimated to be about 50%. The aerosol indirect effect is estimated to be of comparable magnitude to the direct forcing. We find that the magnitude of the forcing declined sharply from 1990 to 2010 (by 0.8 W m−2 direct and 1.0 W m−2 indirect), mainly reflecting decreases in SO2 emissions, and project that it will continue declining post-2010 but at a much slower rate since US SO2 emissions have already declined by almost 60% from their peak. This suggests that much of the warming effect of reducing US anthropogenic aerosol sources has already been realized. The small positive radiative forcing from US BC emissions (+0.3 W m−2 over the eastern US in 2010; 5% of the global forcing from anthropogenic BC emissions worldwide) suggests that a US emission control strategy focused on BC would have only limited climate benefit.en_US
dc.description.sponsorshipEngineering and Applied Sciencesen_US
dc.language.isoen_USen_US
dc.publisherEuropean Geosciences Unionen_US
dc.relation.isversionofdoi:10.5194/acp-12-3333-2012en_US
dc.relation.hasversionhttp://dspace.mit.edu/openaccess-disseminate/1721.1/74087en_US
dash.licenseLAA
dc.titleClimatic Effects of 1950-2050 Changes in US Anthropogenic Aerosols - Part 1: Aerosol Trends and Radiative Forcingen_US
dc.typeJournal Articleen_US
dc.description.versionVersion of Recorden_US
dc.relation.journalAtmospheric Chemistry and Physicsen_US
dash.depositing.authorJacob, Daniel J.
dc.date.available2014-03-17T16:07:52Z
dc.identifier.doi10.5194/acp-12-3333-2012*
workflow.legacycommentsCCBY FAR 2013en_US
dash.contributor.affiliatedLeibensperger, Eric Michael
dash.contributor.affiliatedMickley, Loretta
dash.contributor.affiliatedJacob, Daniel
dc.identifier.orcid0000-0002-6373-3100


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