Lj. Mickley et al., Radiative forcing from tropospheric ozone calculated with a unified chemistry-climate model, J GEO RES-A, 104(D23), 1999, pp. 30153-30172
We have developed a global model for the study of chemistry-climate interac
tions by incorporating a detailed simulation of tropospheric ozone-NO,hydro
carbon chemistry within a general circulation model (GCM). We present a fir
st application of the model to the calculation of radiative forcing from tr
opospheric ozone since preindustrial times. Longwave and shortwave radiatio
n fluxes are computed every 5 hours in the GCM using the locally simulated
ozone fields. In this manner, the model resolves synoptic-scale correlation
s between ozone and meteorological variables. A simulation for present-day
conditions is compared to a preindustrial atmosphere (similar to 1800 A.D.)
with no fossil fuel combustion, 10% of present-day biomass burning, and 0.
7 ppm methane. The two simulations use the same meteorological fields; the
radiative forcing does not feed back into the GCM. The model reproduces wel
l the observed distributions of ozone and its precursors in the present-day
atmosphere. Increases in ozone since preindustrial times are 20-200% depen
ding on region and season. The global mean, instantaneous radiative forcing
from anthropogenic ozone is 0.44 W m(2) (0.35 longwave, 0.09 shortwave). T
he model reveals large shortwave forcings (0.3-0.7 W m(2)) over polar regio
ns in summer. The total forcing is greater than 1.0 W m(2) over large areas
, including the Arctic, during Northern Hemisphere summer. The normalized r
adiative forcing per unit of added ozone column varies globally from -0.01
to 0.05 W m(2). This variance can be explained in large part by the tempera
ture difference between the surface and the tropopause; clouds are an addit
ional factor, particularly at low latitudes. An off-line radiative calculat
ion using the same ozone fields but averaged monthly shows nearly identical
forcings, with differences less than +/-2% over most of the Earth. The sim
ilarity between the off-line and on-line simulations suggests that the comm
on use of off-line ozone fields is acceptable in radiative forcing calculat
ions. Addition of the direct forcings from anthropogenic sulfate aerosol an
d tropospheric ozone computed with the same GCM shows compensating effects,
with sulfate dominating at northern midlatitudes and ozone usually dominat
ing elsewhere.