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Net radiative forcing due to changes in regional emissions of tropospheric ozone precursors

Author(s): Naik, Vaishali; Mauzerall, Denise L.; Horowitz, Larry; Schwarzkopf, M. Daniel; Ramaswamy, V.; et al

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dc.contributor.authorNaik, Vaishali-
dc.contributor.authorMauzerall, Denise L.-
dc.contributor.authorHorowitz, Larry-
dc.contributor.authorSchwarzkopf, M. Daniel-
dc.contributor.authorRamaswamy, V.-
dc.contributor.authorOppenheimer, Michael-
dc.date.accessioned2019-12-19T17:26:14Z-
dc.date.available2019-12-19T17:26:14Z-
dc.date.issued2005en_US
dc.identifier.citationNaik, Vaishali, Mauzerall, Denise, Horowitz, Larry, Schwarzkopf, M. Daniel, Ramaswamy, V., Oppenheimer, Michael. (2005). Net radiative forcing due to changes in regional emissions of tropospheric ozone precursors. Journal of Geophysical Research, 110 (D24), 10.1029/2005JD005908en_US
dc.identifier.issn0148-0227-
dc.identifier.urihttp://arks.princeton.edu/ark:/88435/pr13n2s-
dc.description.abstractThe global distribution of tropospheric ozone (O-3) depends on the emission of precursors, chemistry, and transport. For small perturbations to emissions, the global radiative forcing resulting from changes in O-3 can be expressed as a sum of forcings from emission changes in different regions. Tropospheric O-3 is considered in present climate policies only through the inclusion of indirect effect of CH4 on radiative forcing through its impact on O-3 concentrations. The short-lived O-3 precursors (NOx, CO, and NMHCs) are not directly included in the Kyoto Protocol or any similar climate mitigation agreement. In this study, we quantify the global radiative forcing resulting from a marginal reduction (10%) in anthropogenic emissions of NOx alone from nine geographic regions and a combined marginal reduction in NOx, CO, and NMHCs emissions from three regions. We simulate, using the global chemistry transport model MOZART-2, the change in the distribution of global O-3 resulting from these emission reductions. In addition to the short-term reduction in O-3, these emission reductions also increase CH4 concentrations (by decreasing OH); this increase in CH4 in turn counteracts part of the initial reduction in O-3 concentrations. We calculate the global radiative forcing resulting from the regional emission reductions, accounting for changes in both O-3 and CH4. Our results show that changes in O-3 production and resulting distribution depend strongly on the geographical location of the reduction in precursor emissions. We find that the global O-3 distribution and radiative forcing are most sensitive to changes in precursor emissions from tropical regions and least sensitive to changes from midlatitude and high-latitude regions. Changes in CH4 and O-3 concentrations resulting from NOx emission reductions alone produce offsetting changes in radiative forcing, leaving a small positive residual forcing (warming) for all regions. In contrast, for combined reductions of anthropogenic emissions of NOx, CO, and NMHCs, changes in O-3 and CH4 concentrations result in a net negative radiative forcing (cooling). Thus we conclude that simultaneous reductions of CO, NMHCs, and NOx lead to a net reduction in radiative forcing due to resulting changes in tropospheric O-3 and CH4 while reductions in NOx emissions alone do not.en_US
dc.format.extentD24306 (1-14)en_US
dc.language.isoen_USen_US
dc.relation.ispartofJournal of Geophysical Researchen_US
dc.rightsFinal published version. Article is made available in OAR by the publisher's permission or policy.en_US
dc.titleNet radiative forcing due to changes in regional emissions of tropospheric ozone precursorsen_US
dc.typeJournal Articleen_US
dc.identifier.doidoi:10.1029/2005JD005908-
pu.type.symplectichttp://www.symplectic.co.uk/publications/atom-terms/1.0/journal-articleen_US

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