A model for studies of tropospheric ozone and nonmethane hydrocarbons: Model description and ozone results

被引:1
|
作者
von Kuhlmann, R
Lawrence, MG
Crutzen, PJ
Rasch, PJ
机构
[1] Max Planck Inst Chem, Dept Airchem, D-55020 Mainz, Germany
[2] Natl Ctr Atmospher Res, Boulder, CO 80303 USA
关键词
global model; ozone budget; tropospheric ozone; stratosphere-troposphere exchange; nonmethane hydrocarbons; mass-wind inconsistency;
D O I
10.1029/2002JD002893
中图分类号
P4 [大气科学(气象学)];
学科分类号
0706 ; 070601 ;
摘要
We have developed a global three-dimensional chemistry-meteorology model for studies of ozone and hydrocarbons in the troposphere, called Model of Atmospheric Transport and Chemistry-Max-Planck-Institute for Chemistry Version (MATCH-MPIC). The model currently calculates the distributions of 54 species and 141 reactions using a new flexible chemical integration method in connection with a fast general Rosenbrock solver. The reactions can be easily expanded for future studies with the model. The model includes updated emission inventories, an explicit dry deposition scheme, online photolysis rates, extensive budgeting capabilities and a correction for the so-called "mass-wind inconsistency'' problem. One-year simulations at two different horizontal resolutions, approximately 1.9degrees x 1.9degrees (T63) and 5.6degrees x 5.6degrees (T21), both with 28 vertical levels, are extensively evaluated with available observations from surface stations, ozonesondes, and field campaigns. The model is generally able to reproduce the observations of ozone to within 10 nmol/mol, but it overestimates upper tropospheric ozone at northern high-latitude stations in winter and spring and tends to underestimate the summer maximum in the free troposphere. In the tropics the chemical tropopause is sometimes too low. Generally, the low-resolution run yields only slightly worse agreement with observations compared to the higher-resolution run, thus making it suitable for further sensitivity studies. In a simulation using different meteorological data, O-3 agrees much better with observations in the upper troposphere, possibly because of the higher resolution near the tropopause. The net ozone production integrated over all tropospheric regions with a net production and loss separately reveals that the calculated chemically induced redistribution of ozone in the troposphere is 2-3 times larger than the net stratospheric influx. Even in the upper troposphere, photochemical production is of similar magnitude to the stratospheric influence.
引用
收藏
页数:22
相关论文
共 50 条
  • [21] Tropospheric ozone and skin aging: Results from two German cohort studies
    Fuks, Kateryna B.
    Huels, Anke
    Sugiri, Dorothea
    Altug, Hicran
    Vierkoetter, Andrea
    Abramson, Michael J.
    Goebel, Jan
    Wagner, Gert G.
    Demuth, Ilja
    Krutmann, Jean
    Schikowski, Tamara
    ENVIRONMENT INTERNATIONAL, 2019, 124 : 139 - 144
  • [22] VERTICAL SAMPLING AND ANALYSIS OF NONMETHANE HYDROCARBONS FOR OZONE CONTROL IN URBAN NORTH-CAROLINA
    LAWRIMORE, JH
    DAS, M
    ANEJA, VP
    JOURNAL OF GEOPHYSICAL RESEARCH-ATMOSPHERES, 1995, 100 (D11) : 22785 - 22793
  • [23] Sources and variations of tropospheric ozone in central Siberia: observations and model simulations
    Shtabkin, Yu A.
    Moiseenko, K. B.
    Skorokhod, A., I
    Berezina, E., V
    Vasileva, A. V.
    CLIMATE CHANGE: CAUSES, RISKS, CONSEQUENCES, PROBLEMS OF ADAPTATION AND MANAGEMENT, 2020, 606
  • [24] Origins of tropospheric ozone interannual variation over Reunion: A model investigation
    Liu, Junhua
    Rodriguez, Jose M.
    Thompson, Anne M.
    Logan, Jennifer A.
    Douglass, Anne R.
    Olsen, Mark A.
    Steenrod, Stephen D.
    Posny, Francoise
    JOURNAL OF GEOPHYSICAL RESEARCH-ATMOSPHERES, 2016, 121 (01) : 521 - 537
  • [25] A PHOTOCHEMICAL MODEL OF OZONE INTERFERENCE EFFECTS IN LASER DETECTION OF TROPOSPHERIC OH
    SMITH, GP
    CROSLEY, DR
    JOURNAL OF GEOPHYSICAL RESEARCH-ATMOSPHERES, 1990, 95 (D10) : 16427 - 16442
  • [26] Compact airborne lidar for tropospheric ozone: description and field measurements
    Ancellet, G
    Ravetta, F
    APPLIED OPTICS, 1998, 37 (24): : 5509 - 5521
  • [27] Evaluation of tropospheric ozone and ozone precursors in simulations from the HTAPII and CCMI model intercomparisons - a focus on the Indian subcontinent
    Hakim, Zainab Q.
    Archer-Nicholls, Scott
    Beig, Gufran
    Folberth, Gerd A.
    Sudo, Kengo
    Abraham, Nathan Luke
    Ghude, Sachin
    Henze, Daven K.
    Archibald, Alexander T.
    ATMOSPHERIC CHEMISTRY AND PHYSICS, 2019, 19 (09) : 6437 - 6458
  • [28] Tropospheric Ozone Assessment Report: Present-day distribution and trends of tropospheric ozone relevant to climate and global atmospheric chemistry model evaluation
    Gaudel, A.
    Cooper, O. R.
    Ancellet, G.
    Barret, B.
    Boynard, A.
    Burrows, J. P.
    Clerbaux, C.
    Coheur, P. -F.
    Cuesta, J.
    Cuevas, E.
    Doniki, S.
    Dufour, G.
    Ebojie, F.
    Foret, G.
    Garcia, O.
    Granados-Munoz, M. J.
    Hannigan, J. W.
    Hase, F.
    Hassler, B.
    Huang, G.
    Hurtmans, D.
    Jaffe, D.
    Jones, N.
    Kalabokas, P.
    Kerridge, B.
    Kulawik, S.
    Latter, B.
    Leblanc, T.
    Le Flochmoen, E.
    Lin, W.
    Liu, J.
    Liu, X.
    Mahieu, E.
    McClure-Begley, A.
    Neu, J. L.
    Osman, M.
    Palm, M.
    Petetin, H.
    Petropavlovskikh, I.
    Querel, R.
    Rahpoe, N.
    Rozanov, A.
    Schultz, M. G.
    Schwab, J.
    Siddans, R.
    Smale, D.
    Steinbacher, M.
    Tanimoto, H.
    Tarasick, D. W.
    Thouret, V.
    ELEMENTA-SCIENCE OF THE ANTHROPOCENE, 2018, 6
  • [29] Problem of tropospheric ozone and some results of its measurements
    Belan, B.D.
    Atmospheric and Oceanic Optics(English Edition of the Journal Optika Atmosfery i Okeana), 1996, 9 (09):
  • [30] Model sensitivity studies of Arctic ozone depletion
    Chipperfield, MP
    Pyle, JA
    JOURNAL OF GEOPHYSICAL RESEARCH-ATMOSPHERES, 1998, 103 (D21) : 28389 - 28403