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Global radiative forcing of coupled tropospheric ozone and aerosols in a unified general circulation model

Liao, Hong and Seinfeld, John H. and Adams, Peter J. and Mickley, Loretta J. (2004) Global radiative forcing of coupled tropospheric ozone and aerosols in a unified general circulation model. Journal of Geophysical Research. Atmospheres, 109 (D16). Art. No. D16207. ISSN 2169-897X. https://resolver.caltech.edu/CaltechAUTHORS:20141028-094421952

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Abstract

Global simulations of sea salt and mineral dust aerosols are integrated into a previously developed unified general circulation model (GCM), the Goddard Institute for Space Studies (GISS) GCM II′, that simulates coupled tropospheric ozone-NO_x-hydrocarbon chemistry and sulfate, nitrate, ammonium, black carbon, primary organic carbon, and secondary organic carbon aerosols. The fully coupled gas-aerosol unified GCM allows one to evaluate the extent to which global burdens, radiative forcing, and eventually climate feedbacks of ozone and aerosols are influenced by gas-aerosol chemical interactions. Estimated present-day global burdens of sea salt and mineral dust are 6.93 and 18.1 Tg with lifetimes of 0.4 and 3.9 days, respectively. The GCM is applied to estimate current top of atmosphere (TOA) and surface radiative forcing by tropospheric ozone and all natural and anthropogenic aerosol components. The global annual mean value of the radiative forcing by tropospheric ozone is estimated to be +0.53 W m^(−2) at TOA and +0.07 W m^(−2) at the Earth's surface. Global, annual average TOA and surface radiative forcing by all aerosols are estimated as −0.72 and −4.04 W m^(−2), respectively. While the predicted highest aerosol cooling and heating at TOA are −10 and +12 W m^(−2), respectively, surface forcing can reach values as high as −30 W m^(−2), mainly caused by the absorption by black carbon, mineral dust, and OC. We also estimate the effects of chemistry-aerosol coupling on forcing estimates based on currently available understanding of heterogeneous reactions on aerosols. Through altering the burdens of sulfate, nitrate, and ozone, heterogeneous reactions are predicted to change the global mean TOA forcing of aerosols by 17% and influence global mean TOA forcing of tropospheric ozone by 15%.


Item Type:Article
Related URLs:
URLURL TypeDescription
https://doi.org/10.1029/2003JD004456DOIArticle
https://doi.org/10.1029/2004JD005476DOIErratum
ORCID:
AuthorORCID
Seinfeld, John H.0000-0003-1344-4068
Adams, Peter J.0000-0003-0041-058X
Mickley, Loretta J.0000-0002-7859-3470
Additional Information:Copyright 2004 by the American Geophysical Union. Received 16 December 2003; revised 30 March 2004; accepted 14 June 2004; published 21 August 2004. This work was supported by the NASA Earth Observing System-Interdisciplinary Science Program (NASA EOS-IDS). The authors gratefully acknowledge Joe Prospero and Dennis Savoie for providing sea salt and dust measurements. We thank Brent Holben, Giuseppe Zibordi, Mary J. Bartholomew, Robert Frouin, Didier Tanre, Chuck McClain, and Arnon Karnieli for their effort in maintaining AERONET measurements used in this work. We would also like to acknowledge the Center for Advanced Computing Research at Caltech for computing resources. Corrected by: Aerosol and Clouds: Correction to “Global radiative forcing of coupled tropospheric ozone and aerosols in a unified general circulation model” Vol. 109, Issue D24, Article first published online: 21 DEC 2004
Funders:
Funding AgencyGrant Number
NASAUNSPECIFIED
Subject Keywords:radiative forcing, mineral dust, sea salt
Issue or Number:D16
Classification Code:0305 Atmospheric Composition and Structure: Aerosols and particles (0345, 4801); 0345 Atmospheric Composition and Structure: Pollution—urban and regional (0305); 0365 Atmospheric Composition and Structure: Troposphere—composition and chemistry
Record Number:CaltechAUTHORS:20141028-094421952
Persistent URL:https://resolver.caltech.edu/CaltechAUTHORS:20141028-094421952
Official Citation:Liao, H., J. H. Seinfeld, P. J. Adams, and L. J. Mickley (2004), Global radiative forcing of coupled tropospheric ozone and aerosols in a unified general circulation model, J. Geophys. Res., 109, D16207, doi:10.1029/2003JD004456
Usage Policy:No commercial reproduction, distribution, display or performance rights in this work are provided.
ID Code:50922
Collection:CaltechAUTHORS
Deposited By: George Porter
Deposited On:28 Oct 2014 17:00
Last Modified:21 Feb 2023 23:36

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