Chemical compounds in the remote Pacific troposphere: Comparison between MLOPEX measurements and chemical transport model calculations

被引:42
作者
Brasseur, GP [1 ]
Hauglustaine, DA [1 ]
Walters, S [1 ]
机构
[1] CNRS, SERV AERON, PARIS, FRANCE
关键词
D O I
10.1029/95JD03520
中图分类号
P4 [大气科学(气象学)];
学科分类号
0706 ; 070601 ;
摘要
A global three-dimensional chemical transport model, called MOZART (Model of OZone And Related species in the Troposphere), is used to compare calculated abundances of chemical species and their seasonal evolution in the remote Pacific troposphere near Hawaii with values observed during the Mauna Loa Observatory Photochemistry Experiments (MLOPEX 1 and 2). MOZART is a fully diurnal model which calculates the time evolution of about 30 chemical species from the surface to the upper stratosphere. It accounts for surface emissions of source gases, wet and dry depositions, photochemical transformations and transport processes. The dynamical variables are provided by the National Center for Atmospheric Research (NCAR) Community Climate Model (CCM2) at T42 resolution (2.8 degrees x2.8 degrees) and 18 levels in the vertical. Simulated abundances of Rn-222 reveal an underestimate of the transport of continental emissions to the remote Pacific troposphere, more particularly during winter and summer. Calculated concentrations of chemical species are generally in fair agreement with observations. However, the abundances of soluble species are overestimated, leading, for example, to concentrations of nitric acid (HNO3) and hydrogen peroxide (H2O2) which are overpredicted by a factor of 3-8, depending on the season. This feature is attributed to insufficient washout by clouds and precipitation in the model. MOZART succesfully reproduces the development of high-NOx episodes at Mauna Loa Observatory (MLO) associated with anticyclonic conditions to the north of Hawaii and breakdown of the polar jet which tends to deflect to the central Pacific the how of NOx transported from eastern Asia (China, Japan). During high NOx episodes, the calculated NOx mixing ratio in the vicinity of the MLO increases by about a factor of 3 over its background level (reaching 90-100 pptv) within 3-5 days.
引用
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页码:14795 / 14813
页数:19
相关论文
共 58 条
  • [11] ORIGIN OF TROPOSPHERIC NOX OVER SUB-ARCTIC EASTERN CANADA IN SUMMER
    FAN, SM
    JACOB, DJ
    MAUZERALL, DL
    BRADSHAW, JD
    SANDHOLM, ST
    BLAKE, DR
    SINGH, HB
    TALBOT, RW
    GREGORY, GL
    SACHSE, GW
    [J]. JOURNAL OF GEOPHYSICAL RESEARCH-ATMOSPHERES, 1994, 99 (D8) : 16867 - 16877
  • [12] FEITCHER J, 1990, TELLUS, V42, P100
  • [13] RADON-222 AS A COMPARATIVE TRACER OF TRANSPORT AND MIXING IN 2 GENERAL-CIRCULATION MODELS OF THE ATMOSPHERE
    GENTHON, C
    ARMENGAUD, A
    [J]. JOURNAL OF GEOPHYSICAL RESEARCH-ATMOSPHERES, 1995, 100 (D2) : 2849 - 2866
  • [14] THE RAINOUT PARAMETERIZATION IN A PHOTOCHEMICAL MODEL
    GIORGI, F
    CHAMEIDES, WL
    [J]. JOURNAL OF GEOPHYSICAL RESEARCH-ATMOSPHERES, 1985, 90 (ND5) : 7872 - 7880
  • [15] Hack J. J., 1993, NCARTN382STR
  • [16] Parameterization of moist convection in the National Center for Atmospheric Research community climate model (CCM2)
    Hack, James J.
    [J]. JOURNAL OF GEOPHYSICAL RESEARCH-ATMOSPHERES, 1994, 99 (D3) : 5551 - 5568
  • [17] HACK JJ, 1994, J GEOPHYS RES, V99, P20875
  • [18] KINETICS OF THE REACTION OF NO3 WITH HO2
    HALL, IW
    WAYNE, RP
    COX, RA
    JENKIN, ME
    HAYMAN, GD
    [J]. JOURNAL OF PHYSICAL CHEMISTRY, 1988, 92 (17) : 5049 - 5054
  • [19] HOLTSLAG AAM, 1993, J CLIMATE, V6, P1825, DOI 10.1175/1520-0442(1993)006<1825:LVNBLD>2.0.CO
  • [20] 2