Multimodel ensemble simulations of present-day and near-future tropospheric ozone

被引:594
作者
Stevenson, DS
Dentener, FJ
Schultz, MG
Ellingsen, K
van Noije, TPC
Wild, O
Zeng, G
Amann, M
Atherton, CS
Bell, N
Bergmann, DJ
Bey, I
Butler, T
Cofala, J
Collins, WJ
Derwent, RG
Doherty, RM
Drevet, J
Eskes, HJ
Fiore, AM
Gauss, M
Hauglustaine, DA
Horowitz, LW
Isaksen, ISA
Krol, MC
Lamarque, JF
Lawrence, MG
Montanaro, V
Müller, JF
Pitari, G
Prather, MJ
Pyle, JA
Rast, S
Rodriguez, JM
Sanderson, MG
Savage, NH
Shindell, DT
Strahan, SE
Sudo, K
Szopa, S
机构
[1] Univ Edinburgh, Sch Geosci, Edinburgh EH9 3J9, Midlothian, Scotland
[2] Joint Res Ctr, Inst Environm & Sustainabil, I-21020 Ispra, Italy
[3] Max Planck Inst Meteorol, D-20146 Hamburg, Germany
[4] Univ Oslo, Dept Geosci, N-0316 Oslo, Norway
[5] Royal Netherlands Meteorol Inst, De Bilt, Netherlands
[6] Japan Marine Sci & Technol Ctr, Frontier Res Ctr Global Change, Kanazawa Ku, Yokohama, Kanagawa 2360001, Japan
[7] Univ Cambridge, Ctr Atmospher Sci, Cambridge CB2 1EW, England
[8] Int Inst Appl Syst Anal, A-2361 Laxenburg, Austria
[9] Lawrence Livermore Natl Lab, Div Atmospher Sci, Livermore, CA 94550 USA
[10] NASA, Goddard Inst Space Studies, New York, NY 10025 USA
[11] Ecole Polytech Fed Lausanne, CH-1015 Lausanne, Switzerland
[12] Max Planck Inst Chem, D-55128 Mainz, Germany
[13] Hadley Ctr Climate Predict & Res, Met Off, Exeter EX1 3PB, Devon, England
[14] rdscientific, Newbury RG14 6LH, Berks, England
[15] NOAA, Geophys Fluid Dynam Lab, Princeton, NJ 08540 USA
[16] Lab Sci Climat & Environm, F-91191 Gif Sur Yvette, France
[17] Natl Ctr Atmospher Res, Div Atmospher Chem, Boulder, CO 80307 USA
[18] Univ Aquila, Dipartimento Fis, I-67010 Laquila, Italy
[19] Belgian Inst Space Aeron, B-1180 Brussels, Belgium
[20] Univ Calif Irvine, Dept Earth Syst Sci, Irvine, CA 92697 USA
[21] Univ Miami, Rosenstiel Sch Marine & Atmospher Sci, Miami, FL 33149 USA
[22] NASA, Goddard Space Flight Ctr, Greenbelt, MD USA
基金
英国自然环境研究理事会;
关键词
D O I
10.1029/2005JD006338
中图分类号
P4 [大气科学(气象学)];
学科分类号
0706 ; 070601 ;
摘要
Global tropospheric ozone distributions, budgets, and radiative forcings from an ensemble of 26 state-of-the-art atmospheric chemistry models have been intercompared and synthesized as part of a wider study into both the air quality and climate roles of ozone. Results from three 2030 emissions scenarios, broadly representing "optimistic,'' "likely,'' and "pessimistic'' options, are compared to a base year 2000 simulation. This base case realistically represents the current global distribution of tropospheric ozone. A further set of simulations considers the influence of climate change over the same time period by forcing the central emissions scenario with a surface warming of around 0.7K. The use of a large multimodel ensemble allows us to identify key areas of uncertainty and improves the robustness of the results. Ensemble mean changes in tropospheric ozone burden between 2000 and 2030 for the 3 scenarios range from a 5% decrease, through a 6% increase, to a 15% increase. The intermodel uncertainty (+/-1 standard deviation) associated with these values is about +/-25%. Model outliers have no significant influence on the ensemble mean results. Combining ozone and methane changes, the three scenarios produce radiative forcings of -50, 180, and 300 mW m(-2), compared to a CO2 forcing over the same time period of 800-1100 mW m(-2). These values indicate the importance of air pollution emissions in short-to medium-term climate forcing and the potential for stringent/lax control measures to improve/worsen future climate forcing. The model sensitivity of ozone to imposed climate change varies between models but modulates zonal mean mixing ratios by +/-5 ppbv via a variety of feedback mechanisms, in particular those involving water vapor and stratosphere-troposphere exchange. This level of climate change also reduces the methane lifetime by around 4%. The ensemble mean year 2000 tropospheric ozone budget indicates chemical production, chemical destruction, dry deposition and stratospheric input fluxes of 5100, 4650, 1000, and 550 Tg(O-3) yr(-1), respectively. These values are significantly different to the mean budget documented by the Intergovernmental Panel on Climate Change (IPCC) Third Assessment Report (TAR). The mean ozone burden (340 Tg(O-3)) is 10% larger than the IPCC TAR estimate, while the mean ozone lifetime (22 days) is 10% shorter. Results from individual models show a correlation between ozone burden and lifetime, and each model's ozone burden and lifetime respond in similar ways across the emissions scenarios. The response to climate change is much less consistent. Models show more variability in the tropics compared to midlatitudes. Some of the most uncertain areas of the models include treatments of deep tropical convection, including lightning NOx production; isoprene emissions from vegetation and isoprene's degradation chemistry; stratosphere-troposphere exchange; biomass burning; and water vapor concentrations.
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页数:23
相关论文
共 162 条
  • [1] Emission of trace gases and aerosols from biomass burning
    Andreae, MO
    Merlet, P
    [J]. GLOBAL BIOGEOCHEMICAL CYCLES, 2001, 15 (04) : 955 - 966
  • [2] [Anonymous], 2001, PROJECTIONS FUTURE C
  • [3] [Anonymous], 2001, REPORT INTERGOVERNME
  • [4] [Anonymous], 74 CRTN HADL CTR MET
  • [5] Atmospheric chemistry of VOCs and NOx
    Atkinson, R
    [J]. ATMOSPHERIC ENVIRONMENT, 2000, 34 (12-14) : 2063 - 2101
  • [6] Global modeling of heterogeneous chemistry on mineral aerosol surfaces: Influence on tropospheric ozone chemistry and comparison to observations
    Bauer, SE
    Balkanski, Y
    Schulz, M
    Hauglustaine, DA
    Dentener, F
    [J]. JOURNAL OF GEOPHYSICAL RESEARCH-ATMOSPHERES, 2004, 109 (D2)
  • [7] Impacts of chemistry-aerosol coupling on tropospheric ozone and sulfate simulations in a general circulation model
    Bell, N
    Koch, D
    Shindell, DT
    [J]. JOURNAL OF GEOPHYSICAL RESEARCH-ATMOSPHERES, 2005, 110 (D14) : 1 - 12
  • [8] Global modeling of tropospheric chemistry with assimilated meteorology: Model description and evaluation
    Bey, I
    Jacob, DJ
    Yantosca, RM
    Logan, JA
    Field, BD
    Fiore, AM
    Li, QB
    Liu, HGY
    Mickley, LJ
    Schultz, MG
    [J]. JOURNAL OF GEOPHYSICAL RESEARCH-ATMOSPHERES, 2001, 106 (D19) : 23073 - 23095
  • [9] The oxidative capacity of the troposphere: Coupling of field measurements of OH and a global chemistry transport model
    Bloss, WJ
    Evans, MJ
    Lee, JD
    Sommariva, R
    Heard, DE
    Pilling, MJ
    [J]. FARADAY DISCUSSIONS, 2005, 130 : 425 - 436
  • [10] Bousquet P, 2005, ATMOS CHEM PHYS DISC, V5, P1679