GLOBAL EVOLUTION OF THE MT-PINATUBO VOLCANIC AEROSOLS OBSERVED BY THEINFRARED LIMB-SOUNDING INSTRUMENTS CLAES AND ISAMS ON THE UPPER-ATMOSPHERE RESEARCH SATELLITE
A. Lambert et al., GLOBAL EVOLUTION OF THE MT-PINATUBO VOLCANIC AEROSOLS OBSERVED BY THEINFRARED LIMB-SOUNDING INSTRUMENTS CLAES AND ISAMS ON THE UPPER-ATMOSPHERE RESEARCH SATELLITE, JOURNAL OF GEOPHYSICAL RESEARCH-ATMOSPHERES, 102(D1), 1997, pp. 1495-1512
The cryogenic limb array etalon spectrometer (CLAES) and the improved
stratospheric and mesospheric sounder (ISAMS) instruments on board the
Upper Atmosphere Research Satellite (UARS) have been used to produce
global information on the Mt. Pinatubo volcanic aerosol for the period
from October 1991 to April 1993, The Satellite infrared extinction me
asurements near 12 mu m are converted into the aerosol-related paramet
ers necessary for modelling the effects of the volcanic aerosol on the
aeronomy of the stratosphere and are presented as zonal mean distribu
tions for 80 degrees S to 80 degrees N averaged over similar to 35-day
periods. The aerosol composition is derived from the CLAES and ISAMS
temperature measurements and the water vapour abundances are obtained
from the microwave limb sounder (MLS). The aerosol volume density is o
btained from the extinction measurements from which the Surface area d
ensity and the effective particle radius are estimated. The maximum ae
rosol surface area density has a value of about 50 mu m(2) cm(-3) at a
height of 24 km at the equator in October 1991, before decaying expon
entially with a time constant of 443 +/- 10 days. The surface area den
sity remained well above preeruption values in April 1993. The effecti
ve particle radius in the tropics decays monotonically from 0.65 mu m
in October 1991 to 0.4 mu m in April 1993. The global aerosol sulphate
mass loading is 19.5 Mt in October 1991 and decays exponentially with
a time constant of 342 +/- 8 days to a value of 4.3 Mt by April 1993.
Four months after the eruption the calculated optical thickness at 1.
02 mu m was similar to 0.25 in the tropics. Rate constants are derived
for the heterogeneous reactions of N2O5 and ClONO2 on the sulphate ae
rosols. The application of the aerosol parameters to the investigation
of tracer transport, heterogeneous chemistry, and radiative transfer
is discussed.