The 1991 plinian eruption of Mount Pinatubo (15
N,
120
E) produced 5-10 km
of dacitic pumice fall and
ignimbrite ( Scott et al., in press) and is arguably the
second largest eruption of this century ( Self et al., in
press). Most of the magma was erupted in a 9-hr climactic phase on
June 15, culminating in the formation of a 2.5 km diameter caldera.
Eruption columns exceeded an altitude of 35 km ( Lynch and
Stevens, in press) and formed a giant umbrella cloud that injected
17x10
kg of SO
into the stratosphere ( Bluth et
al., 1992; Read et al., 1993), about twice the amount
produced by the 1982 El Chichón eruption. This SO
is
believed to have come from a water-rich magmatic fluid that
exsolved from the magma during pre-eruption evolution (
Westrich and Gerlach, 1992), rather than directly from the
erupted melt. The SO
formed about 25-30x10
kg of
sulfate (H
SO
) aerosols, which produced the largest
perturbation to the stratospheric aerosol layer since the eruption
of Krakatau in 1883 ( McCormick and Veiga, 1992; Sato et
al., 1993).
The aerosol cloud spread rapidly around the Earth in about three
weeks and attained global coverage after about 1 year. The dense
aerosol cloud caused dramatic decreases in the amount of net
radiation reaching the earth's surface, producing a climate forcing
two times stronger than the aerosols of El Chichón ( Angell
and Korshover, 1983). Resultant climate effects included a
0.5-0.6
C surface cooling in the northern hemisphere,
equivalent to a hemispheric-wide reduction in net radiation of 4
Wm
( Dutton and Christy, 1992; Russell et al., 1993;
Minnis et al., 1993) and a cooling of perhaps as much
as -0.4
C over large parts of the earth in 1992-1993
( Hansen et al., 1992, 1993). The Pinatubo climate forcing
was stronger than the opposing, warming effects of either the El
Niño event or anthropogenic greenhouse gases in the period
1991-1993.
As a result of the high stratospheric aerosol loading,
mid-latitude ozone concentrations reached their lowest recorded
levels during 1992-1993. Startling decreases in ozone abundance
and in the rates of ozone destruction were also observed over
Antarctica in 1991 and 1992. Depletion of southern hemisphere
ozone may have been due in part to the presence of Pinatubo
aerosols but also to the extra aerosols generated by the Mount
Hudson eruption in Chile during August 1991 ( Doiron et al.,
1991; Barton et al., 1992). A sharp decrease in ozone at
9-11 km altitude (approximately at the tropopause) in the austral
spring of 1991 was noted at the time of arrival of the Pinatubo and
Mount Hudson aerosols ( Deshler et al., 1992; Schoeberl
et al., 1993a). The southern hemisphere ``ozone hole'' increased
in 1992 to an unprecedented 27x10
km
in size, and
depletion rates were observed to be faster than ever before
recorded ( Brasseur, 1992; Hofmann et al., 1992, 1994),
raising concern about the amount of biologically destructive
ultraviolet radiation reaching the earth's surface ( Vogelmann
et al., 1992; Smith et al., 1992).
Analysis of the June 1991 eruption of Mt. Pinatubo will provide
a wealth of new information on the dynamics of large eruption
plumes and on the emplacement of pyroclastic flow deposits. A new
post-eruption hazard, secondary pyroclastic flows spawned from
previously emplaced June 1991 ignimbrite during rapid erosion
events, was documented ( Torres et al., in press). Heralding
future trends, much information about the Pinatubo eruptions was
obtained remotely from satellite-borne sensors. These studies
include an analysis of plume structure ( Woods and Self, 1992;
Koyaguchi and Tokuno, 1993) and the long-term trends of
global optical depth ( Stowe et al., 1992), measurements of
SO
using the total ozone mapping spectrometer (TOMS) (
Bluth et al., 1992), other ultra-violet measurements (
McPeters, 1993) and the microwave limb sounder (MLS) ( Read et
al., 1993), and an investigation of the dispersal of stratospheric
aerosols via the stratospheric aerosol and gas experiment (SAGE) II
( Trepte et al., 1993) and the improved stratospheric and
mesospheric sounder (ISAMS) ( Grainger et al., 1993).