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NASA NTRS1984

Chronology, morphology and stratigraphy of pumiceous pyroclastic-flow (ignimbrite) deposits from the eruption of Mount St. Helens on 18 May 1983

Between 1217 and 1620 hours (PDT), on May 18, 1980, the magmatic eruption column of Mount St. Helens formed an ash fountain and pyroclastic flows dominated the eruption process over tephra ejection. Eurption-rate pulsations generally increased to a maximum at 1600 to 1700 hrs. After 1620 hrs, the eruption assumed an open-vent discharge with strong, vertical ejection of tephra. Relative eruption rates (relative mass flux rates) of the pyroclastic flows were determined by correlating sequential photographs and SLAR images, obtained during the eruption, with stratigraphy and surface morphology of the deposits.

Criswell, C. W.↗
NASA NTRS1989

Hydrogen-isotope evidence for extrusion mechanisms of the Mount St Helens lava dome

Hydrogen isotope analyses were used to determine water content and deuterium content for 18 samples of the Mount St Helens dome dacite in an attempt to identify the triggering mechanisms for periodic dome-building eruptions of lava. These isotope data, the first ever collected from an active lava dome, suggest a steady-state process of magma evolution combining crystallization-induced volatile production in the chamber with three different degassing mechanisms: closed-system volatile loss in the magma chamber, open-system volatile release during ascent, and kinetically controlled degassing upon eruption at the surface. The data suggest the future dome-building eruptions may require a new influx of volatile-rich magma into the chamber.

Anderson, Steven W.↗
NASA NTRS1982

Time variations of aerosols in the stratosphere following Mount St. Helens eruptions

Samples of stratospheric aerosols collected with U-2 aircraft for several months following the first three major eruptions of Mount St. Helens were analyzed for ash and liquid acid content. Ash grain sizes and compositions vary depending on collection altitude, location within the drifting cloud, and days following their injection. s computers Size distributions of ash particles vary with altitude. Generally small particles are depleted more rapidly at low altitudes (12 km) than at higher altitudes (17-18 km). Although samples collected 1 day after the first eruption of May 18, 1980, were dry, flow marks on the aircraft indicated parts of the cloud contained heavy acid concentrations. Indeed, all other samples obtained within 1 to 4 days after later eruptions (May 25 and June 12, 1980) were covered with copious amounts of liquid acid. Proportions of liquid to ash varied considerably depending on sampling location and cloud age. Because the acid-coated ash globules were large, they rapidly fell from the stratosphere until, by late June 1980, only a residue of acid droplets remained. Size distributions and concentrations of these droplets varied considerably.

Farlow, N. H.↗
NASA NTRS1982

SAGE measurements of Mount St. Helens volcanic aerosols

The SAGE satellite system was used to make measurements on the optical extinction produced by stratospheric aerosols from the Mount St. Helens eruption. Two periods of observation were analyzed. In the first period (May 21 to 31, 1980), SAGE moved southward from latitude 60 N, and crossed the United States approximately one week after the May 18th eruption. Enhancements in stratospheric extinction were confined to latitudes between about 55 N and 25 N and longitudes between 10 W and 140 W. Individual layers were observed up to altitudes of 23 km. The geographical location of these layers corresponded closely to that expected on the basis of high-altitude meteorological data. During June and much of July, SAGE was, by reason of its geographical position and other orbital characteristics, unable to make further measurements on the northern hemisphere. Between July 19th and August 12th a second southward pass over the northern hemisphere occurred and further observations were made. The volcanic aerosol in the stratosphere was now found to be widely distributed over the hemisphere, the maximum concentrations being north of 50 N. The aerosol showed considerable inhomogeneity and had reached as far south as 15 N but little, if any, had crossed the equator into the southern hemisphere. Individual layers at different heights were still distinguishable. The total stratospheric aerosol loading on this occasion appeared to be greater than in May and corresponded to an increase in global stratospheric mass of between 50 and 100 percent.

Kent, G. S.↗
NASA NTRS1982

Dustsonde measurements of the Mount St. Helens volcanic dust cloud over Wyoming

Numerous balloon soundings of the aerosol and condensation nuclei (CN) concentrations were made over Laramie, Wyoming following the eruption of Mount St. Helens in May of 1980. On several occasions the volatility of the particles was tested. In addition, special instrumentation was used to observe the evolution of particle size after the eruption. The particles in the initial cloud were relatively large and nonvolatile. In a relatively short time, however, the aerosol began showing a dominant volatile component. Although there were probably no CN in the original cloud due to the expected very short coagulation life time, high concentrations of unusually small CN particles were observed about a month after the eruption. By the end of September the CN profiles and associated particle size were practically back to normal. At present the aerosol particles show about a three times larger concentration than before the eruption, most of the new material being in a layer centered around 19 km. The net effect of the more recent series of eruptions during the last half of October 1980 seems to be negligible.

Rosen, J. M.↗
NASA NTRS1981

Trace element composition of the Mount St. Helens plume - Stratospheric samples from the 18 May eruption

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.

Vossler, T.↗
NASA NTRS1982

Forward scattering and backscattering of solar radiation by the stratospheric limb after Mount St. Helens eruption

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.

Ackerman, M.↗
NASA NTRS1982

Ash loading and insolation at Hanford, Washington during and after the eruption of Mount St. Helens

The effects of volcanic ash suspended in the atmosphere on the incident solar radiation was monitored at the Hanford Meteorological Station (HMS) subsequent to the major eruption of Mount St. Helens on May 18, 1980. Passage of the ash plume over Hanford resulted in a very dramatic decrease of solar radiation intensity to zero. A reduction in visibility to less than 1 km was observed, as great quantities of ash fell out of the plume onto the ground. Ash loading in the atmosphere remained very high for several days following the eruption, primarily as a result of resuspension from the surface. Visibilities remained low (2 to 8 km) during this period. Estimates of atmospheric turbidity were made from the ratio of diffuse-to-direct solar radiation; these turbidities were used to estimate extinction along a horizontal path, a quantity which can be related to visibility. Comparisons of observed and estimated visibilities were very good, in spite of the rather coarse approximations used in the estimates. Atmospheric clarity and visibility improved to near pre-eruption conditions following a period of rain showers. The diffuse-to-direct ratio of solar radiation provided a useful index for estimating volcanic ash loading of the atmosphere.

Laulainen, N. S.↗
NASA NTRS1982

Aircraft sampling of the sulfate layer near the tropopause following the eruption of Mount St. Helens

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.

Lezberg, E. A.↗
NASA NTRS1982

Mount St. Helens related aerosol properties from solar extinction measurements

A network of solar radiometers, operated on the North American Continent for an average of 2 years before the first major eruption of Mount St. Helens, Washington, continues to collect direct solar data through the eruptive phase of this volcano. The radiometers collect spectral data through 12 interference filters spanning the sensitivity of the photodiode used as detector. The data are collected every 5 minutes in seven filters and every 15 minutes in five additional filters. A variant of the classical Langley method has been used to measure the optical depth of the aerosols as a function of wavelength. The network, which is the nearest station, is located some 180 kilometers east of the volcano, well within range of noticeable effects during much of the minor as well as major activity. The wavelength dependence of the aerosol-optical depth before and after the 22 July 1980 major eruption, which was well characterized because of favorable meteorological conditions is discussed.

Michalsky, J. J.↗
NASA NTRS1982

Aircraft sampling of the sulfate layer near the tropopause following the eruption of Mount St. Helens

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.

Lezberg, E. A.↗
NASA NTRS1982

Measurements of SO2 in the Mount St. Helens debris

Routine measurements of ozone and SO2 are made with the Dobson and Brewer spectrophotometers at the Atmospheric Environment Service in Downsview Ontario. On May 20 and 21, 1980, large values of column SO2 were observed with both spectrophotometers at the time of passage of the Mount St. Helens debris. Enhanced SO2 values were first observed at 1800Z on May 20. The maximum column amount of SO2 measured was 0.06 cm at 2200 Z. On May 21, SO2 values slowly decreased from 0.03 cm at 1100 Z cm to 0.01 cm at 2000Z. Typical SO2 amounts due to pollution at the Downsview site are approximately 0.003 to 0.005 cm. At the same time of maximum SO2 enhancement, both Dobson and Brewer spectrophotometers measured a 0.040 cm decrease of total ozone. It is not clear whether the decrease of total ozone was caused by the volcanic cloud or natural ozone variability. Air mass trajectories indicate that the altitude of the debris cloud, which passed over Downsview at the time, was between 10 km and 12 km.

Kerr, J. B.↗
NASA NTRS1993

Multi-scale roughness spectra of Mount St. Helens debris flows

A roughness spectrum allows surface structure to be interpreted as a sum of sinusoidal components with differing wavelengths. Knowledge of the roughness spectrum gives insight into the mechanisms responsible for electromagnetic scattering at a given wavelength. Measured spectra from 10-year-old primary debris flow surfaces at Mount St. Helens conform to a power-law spectral model, suggesting that these surfaces are scaling over the measured range of spatial frequencies. Measured spectra from water-deposited surfaces deviate from this model.

Austin, Richard T.↗
NASA NTRS1982

Distribution of Mount St. Helens dust inferred from satellites and meteorological data

Visible and infrared pictures from two Geostationary Operational Environmental Satellite Systems satellites, in circular orbits at about 19,000 nautical miles, are available continuously at approximately 30 minute intervals. Still pictures and film loops from this system vividly depict the events associated with the May 18, 1980 eruption of Mount St. Helens. The initial explosion, shock wave, and visible horizontal dust distribution during the following week are readily apparent. Meteorological wind and height fields permit the inference of the vertical distribution of volcanic dust as well as explain the atmospheric behavior which caused the visible and nonvisible dust distribution.

Laver, J. D.↗
NASA NTRS1982

An incursion of dust in the southwestern United States from April 1980 eruptions of Mount St. Helens

An intrusion of volcanic dust occurred over the northern Mojave Desert, one month before the explosive eruption of 18 May 1980. Visibility was reduced to 15 to 30 miles during meteorological conditions that should have yielded a visibility in excess of 100 miles. This intrusion was documented by particle size distributions, scanning electron microscope analysis of Nuclepore filter samples, insolation measurements, observations by Navy and NASA aircraft, and meteorological data. No further incidents have been observed to date because of a lack of simultaneous volcanic activity with the particular wind patterns that existed in April. Therefore, under certain meteorological conditions, the desert of the southwestern United States could be significantly affected by volcanic ash from an eruption of Mount St. Helens.

Mathews, L. A.↗
NASA NTRS1983

The 1980 eruptions of Mount St. Helens - Physical and chemical processes in the stratospheric clouds

The large and diverse set of observational data collected in the high-altitude plumes of the May 18, May 25, and June 13, 1980 eruptions is organized and analyzed with a view to discerning the processes at work. The data serve to guide and constrain detailed model simulations of the volcanic clouds. For this purpose, use is made of a comprehensive one-dimensional model of stratospheric sulfate aerosols, sulfur precursor gases, and volcanic ash and dust. The model takes into account gas-phase and condensed-phase (heterogeneous) chemistry in the clouds, aerosol nucleation and growth, and cloud expansion. Computational results are presented for the time histories of the gaseous species concentrations, aerosol size distributions, and ash burdens of the eruption clouds. Also investigated are the long-term buildup of stratospheric aerosols in the Northern Hemisphere and the persistent effects of injected chlorine and water vapor on stratospheric ozone. It is concluded that SO2, water vapor, and ash were probably the most important substances injected into the stratosphere by the Mount St. Helens volcano, both with respect to their widespread effects on composition and their effect on climate.

Turco, R. P.↗