Indirect effect of sulfate and carbonaceous aerosols: A mechanistic treatment

被引:162
作者
Lohmann, U [1 ]
Feichter, J
Penner, J
Leaitch, R
机构
[1] Dalhousie Univ, Dept Phys, Halifax, NS B3H 3J5, Canada
[2] Univ Michigan, Dept Atmospher Ocean & Space Sci, Ann Arbor, MI 48109 USA
[3] Meteorol Serv Canada, Downsview, ON M3H 5T4, Canada
[4] Max Planck Inst Meteorol, D-20146 Hamburg, Germany
关键词
D O I
10.1029/1999JD901199
中图分类号
P4 [大气科学(气象学)];
学科分类号
0706 ; 070601 ;
摘要
The indirect effect of anthropogenic aerosols, whereby aerosol particles change cloud optical properties, is the most uncertain component of climate forcing over the past 100 years. Here we use a mechanistic treatment of droplet nucleation and a prognostic treatment of the number of cloud droplets to study the indirect aerosol effect from changes in carbonaceous and sulfate aerosols. Cloud droplet nucleation is parameterized as a function of total aerosol number concentration, updraft velocity, and an activation parameter, which takes into account the mechanism of sulfate aerosol formation. Where previous studies focussed either on sulfate aerosols or carbonaceous aerosols only, here we estimate the combined effect. The combined indirect aerosol effect amounts to -1.1 W m(-2) for an internally mixed aerosol and -1.5 W m(-2) for an externally mixed aerosol compared to -1.4 W m(-2), which we obtained by empirically relating sulfate mass to cloud droplet number. In the case of an internally mixed aerosol, the contribution from increasing carbonaceous and sulfate aerosols is close to being additive as the individual simulations yield an indirect effect of -0.4 W m(-2) due to anthropogenic sulfate aerosols and -0.9 W m(-2) due to anthropogenic carbonaceous aerosols. The contribution of anthropogenic sulfate to the indirect effect is close to zero if an externally mixed aerosol is assumed, while the contribution of carbonaceous aerosols increases to -1.3 W m(-2). The effect of sulfate in the external mixture approach is much smaller than that of carbonaceous aerosols because its burden only increases by a third of that of carbonaceous aerosols and because the mode radius of sulfate is much larger than that of black and organic carbon.
引用
收藏
页码:12193 / 12206
页数:14
相关论文
共 43 条
  • [11] Volcanic sulfur emissions: Estimates of source strength and its contribution to the global sulfate distribution
    Graf, HF
    Feichter, J
    Langmann, B
    [J]. JOURNAL OF GEOPHYSICAL RESEARCH-ATMOSPHERES, 1997, 102 (D9) : 10727 - 10738
  • [12] A GLOBAL-MODEL OF NATURAL VOLATILE ORGANIC-COMPOUND EMISSIONS
    GUENTHER, A
    HEWITT, CN
    ERICKSON, D
    FALL, R
    GERON, C
    GRAEDEL, T
    HARLEY, P
    KLINGER, L
    LERDAU, M
    MCKAY, WA
    PIERCE, T
    SCHOLES, B
    STEINBRECHER, R
    TALLAMRAJU, R
    TAYLOR, J
    ZIMMERMAN, P
    [J]. JOURNAL OF GEOPHYSICAL RESEARCH-ATMOSPHERES, 1995, 100 (D5) : 8873 - 8892
  • [13] Han QY, 1998, J CLIMATE, V11, P1516, DOI 10.1175/1520-0442(1998)011<1516:GSOTRO>2.0.CO
  • [14] 2
  • [15] HAO WM, 1990, ECOL STU AN, V84, P440
  • [16] Chemical apportionment of aerosol column optical depth off the mid-Atlantic coast of the United States
    Hegg, DA
    Livingston, J
    Hobbs, PV
    Novakov, T
    Russell, P
    [J]. JOURNAL OF GEOPHYSICAL RESEARCH-ATMOSPHERES, 1997, 102 (D21) : 25293 - 25303
  • [17] Measurements of the relationship between submicron aerosol number and volume concentration
    Hegg, DA
    Kaufman, YJ
    [J]. JOURNAL OF GEOPHYSICAL RESEARCH-ATMOSPHERES, 1998, 103 (D5) : 5671 - 5678
  • [18] Hess M, 1998, B AM METEOROL SOC, V79, P831, DOI 10.1175/1520-0477(1998)079<0831:OPOAAC>2.0.CO
  • [19] 2
  • [20] Formation of organic aerosols from the oxidation of biogenic hydrocarbons
    Hoffmann, T
    Odum, JR
    Bowman, F
    Collins, D
    Klockow, D
    Flagan, RC
    Seinfeld, JH
    [J]. JOURNAL OF ATMOSPHERIC CHEMISTRY, 1997, 26 (02) : 189 - 222