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Wuebbles, D.J.
Lawrence Livermore National Lab., CA (USA)1981
Lawrence Livermore National Lab., CA (USA)1981
AbstractAbstract
[en] Since the LLNL one-dimensional coupled transport and chemical kinetics model of the troposphere and stratosphere was originally developed in 1972 (Chang et al., 1974), there have been many changes to the model's representation of atmospheric physical and chemical processes. A brief description is given of the current LLNL one-dimensional coupled transport and chemical kinetics model of the troposphere and stratosphere
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Sep 1981; 29 p; Available from NTIS., PC A03/MF A01
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Wuebbles, D.J.
Lawrence Livermore National Lab., CA (United States). Funding organisation: USDOE, Washington, DC (United States)1992
Lawrence Livermore National Lab., CA (United States). Funding organisation: USDOE, Washington, DC (United States)1992
AbstractAbstract
[en] The primary chemicals used as refrigerants, chlorofluorocarbons (CFCs), and the compounds being considered as their replacements (HCFCs and HFCs) have been intensely studied because of concerns about chlorine chemistry effects on stratospheric ozone. Increasing attention is being given to the potential effects of these compounds in concerns about global warming. CFCs, HCFCs, and HFCs absorb infrared radiation and thus are greenhouse gases that can influence radiative forcing on climate. The purpose of this paper is to describe the current understanding of the role of refrigerants in affecting climate. Increasing atmospheric concentrations of CFCs have accounted for about 24 % of the direct increase in radiative forcing from greenhouse gases over the last decade. However, observed decreases in stratospheric ozone, thought to be connected to increasing stratospheric chlorine from CFCs, suggests a cooling tendency over the last decade. This cooling tendency has strong latitudinal gradients, but is, when globally averaged, about comparable in magnitude and opposite in sign to the radiative forcing from CFCs over this period. Because of their shorter atmospheric lifetimes, the direct radiative influence on climate from the replacement compounds should generally be much smaller than the CFCs
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Jun 1992; 21 p; International Institute of Refrigeration meeting on refrigeration, energy and environment; Trondheim (Norway); 22-24 Jun 1992; CONF-9206130--2; CONTRACT W-7405-ENG-48; OSTI as DE92019385; NTIS; INIS; US Govt. Printing Office Dep
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Wuebbles, D.J.
California Univ., Livermore (USA). Lawrence Livermore Lab1980
California Univ., Livermore (USA). Lawrence Livermore Lab1980
AbstractAbstract
[en] The physical structure of the troposphere and stratosphere is the result of an intricate interplay among a large number of radiative, chemical, and dynamical processes. Because it is not possible to model the global environment in the laboratory, theoretical models must be relied on, subject to observational verification, to simulate atmospheric processes. Of particular concern in recent years has been the modeling of those processes affecting the structure of ozone and other trace species in the stratosphere and troposphere. Zonally averaged two-dimensional models with spatial resolution in the vertical and meridional directions can provide a much more realistic representation of tracer transport than one-dimensional models, yet are capable of the detailed representation of chemical and radiative processes contained in the one-dimensional models. The purpose of this study is to describe and analyze existing approaches to representing global atmospheric transport processes in two-dimensional models and to discuss possible alternatives to these approaches. A general description of the processes controlling the transport of trace constituents in the troposphere and stratosphere is given
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Jul 1980; 23 p; Available from NTIS., PC A02/MF A01
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Wuebbles, D.J.
Lawrence Livermore National Lab., CA (USA)1984
Lawrence Livermore National Lab., CA (USA)1984
AbstractAbstract
[en] Comparison of model calculated trends in ozone and temperature due to inferred variations in trace gas concentrations and solar flux, is made with available analyses of observations. In general, the calculated trends in total ozone and the vertical ozone distribution agree well with the measured trends. However, there are too many remaining theoretical and sampling uncertainties to establish causality. Although qualitatively in agreement, the observed temperature decrease in the upper stratosphere is significantly larger than that calculated. Theoretical results suggest a significant influence on stratospheric ozone from solar flux variations, but observational evidence is at best inconclusive. Overall, the trend comparisons tend to be consistent with the hypothesis that several different anthropogenic influences are affecting the present global atmosphere. 7 references, 3 figures, 2 tables
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Aug 1984; 6 p; Quadrennial ozone symposium; Halkidiki (Greece); 3-7 Sep 1984; CONF-8409122--1; Available from NTIS, PC A02/MF A01; 1 as DE84016201
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Wuebbles, D.J.; Jain, A.K.
Lawrence Livermore National Lab., CA (United States). Funding organisation: USDOE, Washington, DC (United States)1993
Lawrence Livermore National Lab., CA (United States). Funding organisation: USDOE, Washington, DC (United States)1993
AbstractAbstract
[en] We carried out essentially all the carbon cycle modeling calculations that were required by the IPCC Working Group 1. Specifically, IPCC required two types of calculations, namely, ''inverse calculations'' (input was CO2 concentrations and the output was CO2 emissions), and the ''forward calculations'' (input was CO2 emissions and output was CO2 concentrations). In particular, we have derived carbon dioxide concentrations and/or emissions for several scenarios using our coupled climate-carbon cycle modelling system
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12 Aug 1993; 19 p; International panel on climate change (IPCC) meeting; Carqueiranne (France); 18 Sep 1993; CONF-9309300--1; CONTRACT W-7405-ENG-48; Also available from OSTI as DE94004332; NTIS; US Govt. Printing Office Dep
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BETA DECAY RADIOISOTOPES, BETA-MINUS DECAY RADIOISOTOPES, CARBON COMPOUNDS, CARBON ISOTOPES, CARBON OXIDES, CHALCOGENIDES, CHEMICAL REACTIONS, EVEN-EVEN NUCLEI, ISOTOPES, LIGHT NUCLEI, NUCLEI, OXIDES, OXYGEN COMPOUNDS, PHOTOCHEMICAL REACTIONS, RADIOACTIVITY, RADIOISOTOPES, SYNTHESIS, YEARS LIVING RADIOISOTOPES
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Connell, P.S.; Wuebbles, D.J.
Lawrence Livermore National Lab., CA (USA)1983
Lawrence Livermore National Lab., CA (USA)1983
AbstractAbstract
[en] This report summarizes the contents and sources of the photochemical and radiative segment of the LLNL one-dimensional transport-kinetics model of the troposphere and stratosphere. Data include the solar flux incident at the top of the atmosphere, absorption spectra for O2, O3 and NO2, and effective absorption coefficients for about 40 photolytic processes as functions of wavelength and, in a few cases, temperature and pressure. The current data set represents understanding of atmospheric photochemical processes as of late 1982 and relies largely on NASA Evaluation Number 5 of Chemical Kinetics and Photochemical Data for Use in Stratospheric Modeling, JPL Publication 82-57 (DeMore et al., 1982). Implementation in the model, including the treatment of multiple scattering and cloud cover, is discussed in Wuebbles (1981)
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Jan 1983; 43 p; Available from NTIS, PC A03/MF A01 as DE83005490
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CARBON COMPOUNDS, CHALCOGENIDES, CHEMISTRY, CHLORINE COMPOUNDS, ELEMENTS, FLUORIDES, FLUORINE COMPOUNDS, HALIDES, HALOGEN COMPOUNDS, NITROGEN COMPOUNDS, NONMETALS, ORGANIC CHLORINE COMPOUNDS, ORGANIC COMPOUNDS, ORGANIC HALOGEN COMPOUNDS, OXIDES, OXYGEN COMPOUNDS, RADIATIONS, SPECTRA, STELLAR RADIATION
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Kinnison, D.E.; Wuebbles, D.J.
Lawrence Livermore National Lab., CA (United States). Funding organisation: USDOE, Washington, DC (United States); National Aeronautics and Space Administration, Washington, DC (United States)1992
Lawrence Livermore National Lab., CA (United States). Funding organisation: USDOE, Washington, DC (United States); National Aeronautics and Space Administration, Washington, DC (United States)1992
AbstractAbstract
[en] Preliminary calculations suggest that heterogeneous reactions are important in calculating the impact on ozone from emissions of trace gases from aircraft fleets. In this study, three heterogeneous chemical processes that occur on background sulfuric acid aerosols are included and their effects on O3, NOx, Clx, HCl, N2O5, ClONO2 are calculated
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5 Jul 1992; 4 p; 1992 quadrennial ozone symposium; Charlottesville, VA (United States); 4-13 Jun 1992; CONF-9206262--1; CONTRACT W-7405-ENG-48; OSTI as DE92019619; NTIS; INIS; US Govt. Printing Office Dep
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Luther, F.M.; Wuebbles, D.J.
California Univ., Livermore (USA). Lawrence Livermore Lab1976
California Univ., Livermore (USA). Lawrence Livermore Lab1976
AbstractAbstract
[en] The effect of including multiple scattering effects in a stratospheric model for computing solar fluxes and photodissociation rates is discussed. It is found that multiple scattering significantly affects photodissociation rates and also model sensitivity to various perturbations depending upon model chemistry, solar zenith angle, and surface albedo. Reaction rates are tabulated, and various parameters and variables are graphed. 6 references
Original Title
Multiple scattering effects
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Dec 1976; 33 p; NASA workshop on CFM assessment; Washington, District of Columbia, United States of America (USA); 10 - 14 Jan 1977; CONF-770131--1; Available from NTIS., PC A03/MF A01
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Wuebbles, D.J.; Chang, J.S.
California Univ., Livermore (USA). Lawrence Livermore Lab1974
California Univ., Livermore (USA). Lawrence Livermore Lab1974
AbstractAbstract
No abstract available
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Jul 1974; 9 p; 2. international conference on the environmental impact of aerospace operations in high atmosphere; San Diego, California, USA; 8 Jul 1974; CONF-740723--1
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Grant, K.E.; Wuebbles, D.J.
Lawrence Livermore National Lab., CA (USA)1988
Lawrence Livermore National Lab., CA (USA)1988
AbstractAbstract
[en] Radiative processes strongly effect equilibrium trace gas concentrations both directly, through photolysis reactions, and indirectly through temperature and transport processes. We have used the LLNL 2-D chemical-radiative-transport model to investigate the net sensitivity of equilibrium ozone concentrations to several changes in radiative forcing. Doubling CO2 from 300 ppmv to 600 ppmv resulted in a temperature decrease of 5 K to 8 K in the middle stratosphere along with an 8% to 16% increase in ozone in the same region. Replacing our usual shortwave scattering algorithms with a simplified Rayleigh algorithm led to a 1% to 2% increase in ozone in the lower stratosphere. Finally, modifying our normal CO2 cooling rates by corrections derived from line-by-line calculations resulted in several regions of heating and cooling. We observed temperature changes on the order of 1 K to 1.5 K with corresponding changes of 0.5% to 1.5% in O3. Our results for doubled CO2 compare favorably with those by other authors. Results for our two perturbation scenarios stress the need for accurately modeling radiative processes while confirming the general validity of current models. 15 refs., 5 figs
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Aug 1988; 4 p; International Quadrennial ozone symposium; Goettingen (Germany, F.R.); 8-13 Aug 1988; CONF-8808102--1; Available from NTIS, PC A02/MF A01; 1 as DE88015434; Portions of this document are illegible in microfiche products.
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