Mount Agung eruption provides test of a global climate perturbation
The Mt. Agung volcanic eruption in 1963 is used as a test case to examine the climatic response to a global-scale radiative perturbation of the earth's atmosphere.
SEARCH · Engineering Papers
Search indexed NASA NTRS and DOE OSTI research on propulsion, heat transfer, battery materials and energy systems. Follow report and document links to the original sources.
Quote a phrase for an exact phrase match. Source license links do not imply unrestricted reuse.
The Mt. Agung volcanic eruption in 1963 is used as a test case to examine the climatic response to a global-scale radiative perturbation of the earth's atmosphere.
Recent near infrared observations have been obtained of the peculiar eruptive variable HM Sagittae which show a general decrease in the flux levels between 1 and 5 microns during 1977-1978. The existing data are yet too sparse to ascertain the nature of the variability; however, both the IR and visual observations confirm the close resemblance of HM Sge to V1016 Cyg. A model of a binary symbiotic system containing a late type variable may be consistent with the current data.
Simple physical arguments are used to show that basaltic volcanos on different planetary bodies would fountain to the same height if the mole fraction of gas in the magma scaled with the acceleration of gravity. It is suggested that the actual eruption velocities and fountain heights are controlled by the velocities of sound in the two phase gas/liquid flows. These velocities are in turn determined by the gas contents in the magma. Predicted characteristics of Hawaiian volcanos are in excellent accord with observations. Assuming that the only gas in lunar volcano is the CO which would be produced if the observed Fe metal in lunar basalts resulted from graphite reduction, lunar volcanos would fountain vigorously, but not as spectacularly as their terrestrial counterparts. The volatile trace metals, halogens, and sulfur released would be transported over the entire moon by the transient atmosphere. Orange and black glass type pyroclastic materials would be transported in sufficient amounts to produce the observed dark mantle deposits.
In a controlled experiment a ground photometer and radar station recorded an increase in night sky luminescence following injection of an electron beam into the atmosphere from a rocket at altitudes 80 to 154 km. A main and supplementary scattering and luminescene regions were observed. The effect is presumed to be due to electron eruption induced by artificial action on the magnetosphere.
The plume of the major eruption of Mount St. Helens on May 18, 1980 penetrated 10 to 11 km into the stratosphere, attaining heights of 22 to 23 km. Wind shears rapidly converted the plume from an expanding vertical cone to a thin, slightly inclined lamina. The lamina was extruded zonally in the stratosphere as the lower part moved eastward at jet stream velocities, while the upper part slowly moved westward in the region of nonsteady transition from the westerlies to the summer stratospheric easterlies. Trajectories computed to position the NASA U-2 aircraft for sampling in the plume are described. Plume volume after 8 hours of strong volcanic emission is estimated at 2,000,000 cu km. Only about 1% of this volume is attributed to the volcano; the rest was entrained from the environment.
Measurements in the stratosphere of gaseous constituents in the plume of Mount St. Helens were obtained during five flights of the NASA U-2 aircraft between 19 May and 17 June 1980. Mixing ratios from gas chromatographic measurements on samples acquired about 24 hours after the initial eruption show considerable enhancement over nonvolcanic concentrations for sulfur dioxide (more than 1000 times), methyl chloride (about 10 times), and carbon disulfide (more than 3 times). The mixing ratio of carbonyl sulfide was comparable to nonvolcanic mixing ratios although 3 days later it was enhanced two to three times. Ion chromatography measurements on water-soluble constituents are also reported. Very large concentrations of chloride, nitrate, and sulfate ions were measured, implying large mixing ratios for the water-soluble gaseous constituents from which the anions are derived. Measurements of radon-222 present in the plume are also reported.
Atmospheric particulate material collected from the stratosphere in the plume of the 18 May 1980 eruption of the Mount St. Helens volcano was quite similar in composition to that of ash that fell to the ground in western Washington. However, there were small but significant differences in concentrations of some elements with altitude, indicating that the stratospheric material was primarily produced from fresh magma, not fragments of the mountain.
A quadruple long exposure of Io in eclipse exhibits faint auroral emission from the eruptive plumes. No luminous spots in the vents, predicted by Gold, were observed. Heat from the interior of Io appears to be the predominant source of energy in the plume.
The ascent and emplacement of basaltic magma on the earth and moon is modeled by the application of geological and physical observations and constraints. Relatively simple mathematical models of the motion of gas/liquid mixtures are shown to be adequate in the treatment of basaltic eruptions, provided that allowance is made for the coalescence of gas bubbles and that realistic geological and petrochemical constraints are applied to the numerical values of variables. Because gas exsolution from magmas on the earth and moon commonly occur at depths of less than 2 km, it is generally convenient to consider separately the rise of bubble-free magmatic liquid at depth in a planetary crust and the more complex motions occurring near the surface with gas exsolution.
The 1883 eruption of Krakatau was a modest ignimbrite-forming event. The deposits are primarily coarse-grained dacitic, non-welded ignimbrite. Large explosions produced pyroclastic flows that entered the sea, generating destructive tsunami. Grain-size studies of the ignimbrite suggest that these explosions were not driven by magma-seawater interaction. The total bulk volume of pyroclastic deposits, including co-ignimbrite ash, is estimated to be 18-21 cu km.
The quasi-steady evolution of solar magnetic fields in response to gradual photospheric changes is considered, with particular attention given to the threshold of a sudden eruption in the solar atmosphere. The formal model of an evolving, force-free field dependent on two Cartesian coordinates is extended to a field which is not force free but in static equilibrium with plasma pressure and gravity. The basic physics is illustrated through the evolution of a loop-shaped electric current sheet enclosing a potential bipolar field with footpoints rooted in the photosphere. A free-boundary problem is posed and then solved for the equilibrium configuration of the current sheet in a hydrostatically supported isothermal atmosphere. As the footpoints move apart to spread a constant photospheric magnetic flux over a larger region, the equilibria available extend the field to increasing heights.
Aerosol samples collected from the April 17, 1979 eruption plume of Soufriere, St. Vincent, at altitudes between 1.8 and 5.5 kilometers were physically and chemically very similar to the ash that fell on the island. Higher altitude samples (7.3 and 9.5 kilometers) had a much lower ash content but comparable concentrations of sulfate, which were above the background concentration found at these altitudes.
Twenty-three filter sampling flights of the NASA Lewis F-106 aircraft, were conducted in the Great Lakes region between June 4 and Dec. 23, 1980, following the major eruption of Mount St. Helens on May 18. The IPC-1478 filters were exposed over an altitude range spanning the local tropopause. A filter sample exposed above the tropopause on June 5 indicated a sulfate level 50 times the baseline measurements, which is consistent with the trajectory predictions of the leading edge of the cloud on its second transit around the earth. Subsequent measurements over a period of 7 months revealed the existence of a layer of sulfate above the tropopause that decayed to a level of about 4 times previously measured background levels by the beginning of August. Concentration of nitrate above the tropopause exhibited considerable variability and showed some enhancement compared with previously measured concentration levels. On the basis of the null results of X ray fluorescence measurements, there is no evidence of ash particle concentrations of greater than 3.4 microns/cu m persisting in the layer above the tropopause following the second transit of the cloud.
The impact of the May 18, 1980 Mount St. Helens eruption on ecosystems is discussed. Special attention is given to its effect on soils, crops, insects, animals, and forests.
Nineteen stratospheric samples from the eruption plumes of Mount St. Helens were collected in five flight experiments. The plume samples were collected at various altitudes from 13.1 to 20.7 km by using the Ames cryogenic sampling system on board the NASA U-2 aircraft. The enriched, cryogenically collected samples were analyzed by chromatography. The concentrations of aerosols precursor gases (OCS, SO2, and CS2), CH3Cl, N2O, CF2Cl2, and CFCl3 were measured by gas chromatography. Large enhancement of the mixing ratio of SO2 and moderate enhancement of CS2 and OCS were found in the plume samples compared with similar measurement under pre-volcanic conditions. A fast decay rate of the SO2 mixing ratio in the plume was observed. Measurement of Cl(-), SO2(2-), and NO3(-) by ion chromatography was also carried out on water solutions prepared from the plume samples. The results obtained with this technique imply large mixing ratios of HCl, (NO + NO2 + HNO3), and SO2, in which these constituents are the respective sources of the anions. Measurement of the Rn222 concentration in the plume was made. Other stratospheric constituents in the plume samples, such as H2O, CO2, CH4, and CO, were also observed.
Twenty filter sampling flights of the NASA Lewis F-106 aircraft were conducted in the Great Lakes region between June 4 and August 8, 1980, following the major eruption of Mount St. Helens, Washington on May 18. The IPC-1478 filters were exposed over an altitude range spanning the local tropopause. Quarter sections were analyzed for sulfate and nitrate by ion chromatography and selected samples were analyzed for chloride by selective ion electrode. Trace elements were searched by X-ray fluorescence analysis. A filter sample taken above the tropopause on June 5 indicated a sulfate level of 50 times the baseline measurements. Subsequent measurements over a period of 2 months showed an initial dropoff and formation of a persistent layer of sulfate above the tropopause with a concentration of 10 to 18 times previously measured background-levels. Concentrations of nitrate above the tropopause exhibited considerable variability and some enhancement compared with previously measured concentration levels. It is suggested that the source of the nitrate may also be volcanic as evidenced by its temporal relationship to the sulfate concentration changes. Based on the null results of X-ray fluorescence measurements, there is no evidence of ash particle concentrations greater than 3.4 microns g/cubic m persisting in the layer above the tropopause after the second transit of the cloud.
Airborne solids concentrations were measured on a near daily basis at two Hanford, Washington sites after the eruption of Mount St. Helens on May 18, 1980. These sites are about 211 km east of Mount St. Helens. Collected airborne solids included resuspended volcanic ash plus normal ambient solids. Average airborne solids concentrations were greater at the Hanford meteorological station sampling site which is 24 km northwest of the Horn Rapids dam sampling site. These increased concentrations reflect the sampling site proximity to greater ash fallout depths. Both sites are in low ash fallout areas although the Hanford meteorological station site is closer to the greater ash fallout areas. Airborne solids concentrations were decreased by rain, but airborne solids concentrations rapidly increased as surfaces dried. Airborne concentrations tended to become nearly the same at both sampling sites only for July 12 and 13.
Stratospheric limb radiance profiles versus altitude of closest approach of the line of sight to the Earth's surface have been measured before and after the Mount St. Helens eruptions by means of photographs taken from a Sun-oriented balloon gondola floating above 35 km altitude over France. Preliminary data were reported for flights in October 1979 and in May and June 1980. The radiance integrated along the line of sight as in-situ radiance (R) can be derived taking into account absorption by ozone and air. The onion peeling inversion method was used to derive the vertical radiance (R) profiles respectively. The values of R were determined in the solar azimuth. The solar elevation angles are chosen larger for the backscattering observation than for the forward scattering observation to deal with as similar illumination conditions as possible despite the Earth's sphericity.