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Long-Term Changes in Lower Tropospheric Baseline Ozone Concentrations:Two recent papers have quantified long-term ozone (O3) changes observed at northernmidlatitude sites that are believed to represent baseline (here understood as representative of continental to hemispheric scales) conditions. Three chemistry-climate models (NCAR CAM-chem, GFDL-CM3, and GISS-E2-R) have calculated retrospective tropospheric O3 concentrations as part of the Atmospheric Chemistry and Climate Model Intercomparison Project and Coupled Model Intercomparison Project Phase 5 model intercomparisons. We present an approach for quantitative comparisons of model results with measurements for seasonally averaged O3 concentrations. There is considerable qualitative agreement between the measurements and the models, but there are also substantial and consistent quantitative disagreements. Most notably, models (1) overestimate absolute O3 mixing ratios, on average by approximately 5 to 17 ppbv in the year 2000, (2) capture only approximately 50% of O3 changes observed over the past five to six decades, and little of observed seasonal differences, and (3) capture approximately 25 to 45% of the rate of change of the long-term changes. These disagreements are significant enough to indicate that only limited confidence can be placed on estimates of present-day radiative forcing of tropospheric O3 derived from modeled historic concentration changes and on predicted future O3 concentrations. Evidently our understanding of tropospheric O3, or the incorporation of chemistry and transport processes into current chemical climate models, is incomplete. Modeled O3 trends approximately parallel estimated trends in anthropogenic emissions of NO(sub x), an important O3 precursor, while measured O3 changes increase more rapidly than these emission estimates.
Document ID
20150000350
Acquisition Source
Goddard Space Flight Center
Document Type
Reprint (Version printed in journal)
External Source(s)
Authors
Parrish, D. D.
(National Oceanic and Atmospheric Administration Boulder, CO, United States)
Lamarque, J.-F.
(National Center for Atmospheric Research Boulder, CO, United States)
Naik, V.
(University Corp. for Atmospheric Research Boulder, CO, United States)
Horowitz, L.
(Princeton Univ. NJ, United States)
Shindell, D. T.
(NASA Goddard Inst. for Space Studies New York, NY United States)
Staehelin, J.
(Institute for Atmospheric and Climate Science Zurich, Switzerland)
Derwent, R.
(rdscientific Newbury, Berkshire, United Kingdom)
Cooper, O. R.
(National Oceanic and Atmospheric Administration Boulder, CO, United States)
Tanimoto, H.
(National Inst. for Environmental Studies Tsukuba, Japan)
Volz-Thomas, A.
(Institute for Energy and Climate Research Juelich, Germany)
Gilge, S.
(Meteorologisches Observatorium Hohenpeissenberg, Germany)
Scheel, H.-E.
(Karlsruhe Inst. of Technology Germany)
Steinbacher, M.
(EMPA Dubendorf Dubendorf, Switzerland)
Frohlich, M.
(Umweltbundesamt Berlin, Germany)
Date Acquired
January 12, 2015
Publication Date
May 13, 2014
Publication Information
Publication: Journal of Geophysical Research: Atmospheres
Publisher: Wiley
Volume: 119
Issue: 9
Subject Category
Geophysics
Report/Patent Number
GSFC-E-DAA-TN18647
Report Number: GSFC-E-DAA-TN18647
Funding Number(s)
WBS: WBS 509496.02.08.04.24
Distribution Limits
Public
Copyright
Public Use Permitted.
Keywords
atmospheric composition
estimates
troposphere
ozone
trends
climate models
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