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William I. Rose

Publications and source records attributed to William I. Rose.

12 recordsLinked to original sources

Downstream aggradation owing to lava dome extrusion and rainfall runoff at Volcán Santiaguito, Guatemala

Persistent lava extrusion at the Santiaguito dome complex (Guatemala) results in continuous lahar activity and river bed aggradation downstream of the volcano. We present a simple method that uses vegetation indices extracted from Landsat Thematic Mapper (TM) data to map impacted zones. Application of this technique to a time series of 21 TM images acquired between 1987 and 2000 allow us to map, measure, and track temporal and spatial variations in the area of lahar impact and river aggradation. In the proximal zone of the fluvial system, these data show a positive correlation between extrusion rate at Santiaguito (E), aggradation area 12 months later (A prox ), and rainfall during the intervening 12 months (Rain12): A prox =3.92+0.50 E+0.31 ln(Rain12) (r 2 =0.79). This describes a situation in which an increase in sediment supply (extrusion rate) and/or a means to mobilize this sediment (rainfall) results in an increase in lahar activity (aggraded area). Across the medial zone, we find a positive correlation between extrusion rate and/or area of proximal aggradation and medial aggradation area ( A med ): A med =18.84-0.05 A prox - 6.15 Rain12 ( r 2 =0.85). Here the correlation between rainfall and aggradation area is negative. This describes a situation in which increased sediment supply results in an increase in lahar activity but, because it is the zone of transport, an increase in rainfall serves to increase the transport efficiency of rivers flowing through this zone. Thus, increased rainfall flushes the medial zone of sediment. These quantitative data allow us to empirically define the links between sediment supply and mobilization in this fluvial system and to derive predictive relationships that use rainfall and extrusion rates to estimate aggradation area 12 months hence.

Volcán Santiaguito

Volcanic hazards at Atitlan volcano, Guatemala

Atitlan Volcano is in the Guatemalan Highlands, along a west-northwest trending chain of volcanoes parallel to the mid-American trench. The volcano perches on the southern rim of the Atitlan caldera, which contains Lake Atitlan. Since the major caldera-forming eruption 85 thousand years ago (ka), three stratovolcanoes--San Pedro, Toliman, and Atitlan--have formed in and around the caldera. Atitlan is the youngest and most active of the three volcanoes. Atitlan Volcano is a composite volcano, with a steep-sided, symmetrical cone comprising alternating layers of lava flows, volcanic ash, cinders, blocks, and bombs. Eruptions of Atitlan began more than 10 ka [1] and, since the arrival of the Spanish in the mid-1400's, eruptions have occurred in six eruptive clusters (1469, 1505, 1579, 1663, 1717, 1826-1856). Owing to its distance from population centers and the limited written record from 200 to 500 years ago, only an incomplete sample of the volcano's behavior is documented prior to the 1800's. The geologic record provides a more complete sample of the volcano's behavior since the 19th century. Geologic and historical data suggest that the intensity and pattern of activity at Atitlan Volcano is similar to that of Fuego Volcano, 44 km to the east, where active eruptions have been observed throughout the historical period. Because of Atitlan's moderately explosive nature and frequency of eruptions, there is a need for local and regional hazard planning and mitigation efforts. Tourism has flourished in the area; economic pressure has pushed agricultural activity higher up the slopes of Atitlan and closer to the source of possible future volcanic activity. This report summarizes the hazards posed by Atitlan Volcano in the event of renewed activity but does not imply that an eruption is imminent. However, the recognition of potential activity will facilitate hazard and emergency preparedness.

Open-File Report

Advantageous GOES IR results for ash mapping at high latitudes: Cleveland eruptions 2001

The February 2001 eruption of Cleveland Volcano, Alaska allowed for comparisons of volcanic ash detection using two‐band thermal infrared (10–12 μm) remote sensing from MODIS, AVHRR, and GOES 10. Results show that high latitude GOES volcanic cloud sensing the range of about 50 to 65°N is significantly enhanced. For the Cleveland volcanic clouds the MODIS and AVHRR data have zenith angles 6–65 degrees and the GOES has zenith angles that are around 70 degrees. The enhancements are explained by distortion in the satellite view of the cloud's lateral extent because the satellite zenith angles result in a “side‐looking” aspect and longer path lengths through the volcanic cloud. The shape of the cloud with respect to the GOES look angle also influences the results. The MODIS and AVHRR data give consistent retrievals of the ash cloud evolution over time and are good corrections for the GOES data.

Alaska

Volcano hazards at Fuego and Acatenango, Guatemala

The Fuego-Acatenango massif comprises a string of five or more volcanic vents along a north-south trend that is perpendicular to that of the Central American arc in Guatemala. From north to south known centers of volcanism are Ancient Acatenango, Yepocapa, Pico Mayor de Acatenango, Meseta, and Fuego. Volcanism along the trend stretches back more than 200,000 years. Although many of the centers have been active contemporaneously, there is a general sequence of younger volcanism, from north to south along the trend. This massive volcano complex towers more than 3500 meters (m) above the Pacific coastal plain to the south and 2000 m above the Guatemalan Highlands to the north. The volcano complex comprises remnants of multiple eruptive centers, which periodically have collapsed to form huge debris avalanches. The largest of these avalanches extended more than 50 kilometers (km) from its source and covered more than 300 square km. The volcano has potential to produce huge debris avalanches that could inundate large areas of the Pacific coastal plain. In areas around the volcanoes and downslope toward the coastal plain, more than 100,000 people are potentially at risk from these and other flowage phenomena.

Acatenango;Fuego

Comparison of TOMS and AVHRR volcanic ash retrievals from the August 1992 eruption of Mt. Spurr

On August 19, 1992, the Advanced Very High Resolution Radiometer (AVHRR) onboard NOAA-12 and NASA's Total Ozone Mapping Spectrometer (TOMS) onboard the Nimbus-7 satellite simultaneously detected and mapped the ash cloud from the eruption of Mt. Spurr, Alaska. The spatial extent and geometry of the cloud derived from the two datasets are in good agreement and both AVHRR split window IR (11-12??m brightness temperature difference) and the TOMS UV Aerosol Index (0.34-0.38??m ultraviolet backscattering and absorption) methods give the same range of total cloud ash mass. Redundant methods for determination of ash masses in drifting volcanic clouds offer many advantages for potential application to the mitigation of aircraft hazards.

Geophysical Research Letters

Early evolution of a stratospheric volcanic eruption cloud as observed with TOMS and AVHRR

This paper is a detailed study of remote sensing data from the total ozone mapping spectrometer (TOMS) and the advanced very high resolution radiometer (AVHRR) satellite detectors, of the 1982 eruption of El Chichón, Mexico. The volcanic cloud/atmosphere interactions in the first four days of this eruption were investigated by combining ultraviolet retrievals to estimate the mass of sulfur dioxide in the volcanic cloud [ Krueger et al. , 1995] with thermal infrared retrievals of the size, optical depth, and mass of fine-grained (1–10 μm radius) volcanic ash [ Wen and Rose , 1994]. Our study provides the first direct evidence of gravitational separation of ash from a stratospheric, gas-rich, plinian eruption column and documents the marked differences in residence times of volcanic ash and sulfur dioxide in volcanic clouds. The eruption column reached as high as 32 km [ Carey and Sigurdsson , 1986] and was injected into an atmosphere with a strong wind shear, which allowed for an observation of the separation of sulfur dioxide and volcanic ash. The upper, more sulfur dioxide-rich part of the cloud was transported to the west in the stratosphere, while the fine-grained ash traveled to the south in the troposphere. The mass of sulfur dioxide released was estimated at 7.1 × 10 9 kg with the mass decreasing by approximately 4% 1 day after the peak. The mass of fine-grained volcanic ash detected was estimated at 6.5 × 10 9 kg, amounting to about 0.7% of the estimated mass of the ash which fell out in the mapped ash blanket close to the volcano. Over the following days, 98% of this remaining fine ash was removed from the volcanic cloud, and the effective radius of ash in the volcanic cloud decreased from about 8 μm to about 4 μm.

Journal of Geophysical Research D: Atmospheres

SO2 from episode 48A eruption, Hawaii: Sulfur dioxide emissions from the episode 48A East Rift Zone eruption of Kilauea volcano, Hawaii

An SO2 flux of 1170??400 (1??) tonnes per day was measured with a correlation spectrometer (COSPEC) in October and November 1986 from the continuous, nonfountaining, basaltic East Rift Zone eruption (episode 48A) of Kilauea volcano. This flux is 5-27 times less than those of highfountaining episodes, 3-5 times greater than those of contemporaneous summit emissions or interphase Pu'u O'o emissions, and 1.3-2 times the emissions from Pu'u O'o alone during 48A. Calculations based on the SO2 emission rate resulted in a magma supply rate of 0.44 million m3 per day and a 0.042 wt% sulfur loss from the magma upon eruption. Both of these calculated parameters agree with determinations made previously by other methods. ?? 1989 Springer-Verlag.

Bulletin of Volcanology

Volatilization, transport and sublimation of metallic and non-metallic elements in high temperature gases at Merapi Volcano, Indonesia

Condensates, silica tube sublimates and incrustations were sampled from 500–800°C fumaroles and lava samples were collected at Merapi Volcano, Indonesia in Jan.–Feb., 1984. With respect to the magma, Merapi gases are enriched by factors greater than 10 5 in Se, Re, Bi and Cd; 10 4 –10 5 in Au, Br, In, Pb and W; 10 3 –10 4 in Mo, Cl, Cs, S, Sn and Ag; 10 2 –10 3 in As, Zn, F and Rb; and 1–10 2 in Cu, K, Na, Sb, Ni, Ga, V, Fe, Mn and Li. The fumaroles are transporting more than 10 6 grams/day ( g d "> gd ) of S, Cl and F; 10 4 –10 6 g/d of Al, Br, Zn, Fe, K and Mg; 10 3 –10 4 g d "> gd of Pb, As, Mo, Mn, V, W and Sr; and less than 10 3 g d "> gd of Ni, Cu, Cr, Ga, Sb, Bi, Cd, Li, Co and U. With decreasing temperature (800-500°C) there were five sublimate zones found in silica tubes: 1) cristobalite and magnetite (first deposition of Si, Fe and Al); 2) K-Ca sulfate, acmite, halite, sylvite and pyrite (maximum deposition of Cl, Na, K, Si, S, Fe, Mo, Br, Al, Rb, Cs, Mn, W, P, Ca, Re, Ag, Au and Co); 3) aphthitalite (K-Na sulfate), sphalerite, galena and Cs-K. sulfate (maximum deposition of Zn, Bi, Cd, Se and In; higher deposition of Pb and Sn); 4) Pb-K chloride and Na-K-Fe sulfate (maximum deposition of Pb, Sn and Cu); and 5) Zn, Cu and K-Pb sulfates (maximum deposition of Pb, Sn, Ti, As and Sb). The incrustations surrounding the fumaroles are also chemically zoned. Bi, Cd, Pb, W, Mo, Zn, Cu, K, Na, V, Fe and Mn are concentrated most in or very close to the vent as expected with cooling, atmospheric contamination and dispersion. The highly volatile elements Br, Cl, As and Sb are transported primarily away from high temperature vents. Ba, Si, P, Al, Ca and Cr are derived from wall rock reactions. Incomplete degassing of shallow magma at 915°C is the origin of most of the elements in the Merapi volcanic gas, although it is partly contaminated by particles or wall rock reactions. The metals are transported predominantly as chloride species. As the gas cools in the fumarolic environment, it becomes saturated with sublimate phases that fractionate from the gas in the order of their equilibrium saturation temperatures. Devolatilization of a cooling batholith could transport enough acids and metals to a hydrothermal system to play a significant role in forming an ore deposit. However, sublimation from a high temperature, high velocity carrier gas is not efficient enough to form a large ore deposit. Re, Se, Cd and Bi could be used as supporting evidence for magmatic fluid transport in an ore deposit.

Geochimica et Cosmochimica Acta

Quaternary silicic pyroclastic deposits of Atitlán Caldera, Guatemala

Atitlán caldera has been the site of several silicic eruptions within the last 150,000 years, following a period of basalt/andesite volcanism. The silicic volcanism began with 5–10 km 3 of rhyodacites, erupted as plinian fall and pyroclastic flows, about 126,000 yr. B.P. At 85,000 yr. B.P. 270–280 km 3 of compositionally distinct rhyolite was erupted in the Los Chocoyos event which produced widely dispersed, plinian fall deposits and widespread, mobile pyroclastic flows. In the latter parts of this eruption rhyodacite and minor dacite were erupted which compositionally resembled the earliest silicic magmas of the Atitlán center. As a result of this major eruption, the modern Atitlán (III) caldera formed. Following this event, rhyodacites were again erupted in smaller (5–13 km 3 ) volumes, partly through the lake, and mafic volcanism resumed, forming three composite volcanoes within the caldera. The bimodal mafic/silicic Atitlán volcanism is similar to that which has occurred elsewhere in the Guatemalan Highlands, but is significantly more voluminous. Mafic lavas are thought to originate in the mantle, but rise, intrude and underplate the lower crust and partly escape to the surface. Eventually, silicic melts form in the crust, possibly partly derived from underplated basaltic material, rise, crystallize and erupt. The renewed mafic volcanism could reflect either regional magmato-tectonic adjustment after the large silicic eruption or the onset of a new cycle.

Journal of Volcanology and Geothermal Research

Inter-laboratory comparison of X-ray fluorescence analyses of eruptive products of El Chichón Volcano, Chiapas, Mexico

An inter-laboratory comparison has been made of X-ray fluorescence analyses of 10 samples of lava and pumices from El Chichón Volcano, Chiapas, Mexico. Some determinations of major-element constituents agree within analytical uncertainty, whereas others exchibit significant bias. Analyses carried out at the Michigan Technological University (MTU) laboratory are systematically lower in MgO (26–48%), Fe total (5–18%), CaO (4–15%) and higher in K 2 O (0–15%) than analyses made at the U.S. Geological Survey (USGS) Denver laboratory. These differences are ascribed in part to a complex combination of calibration assumptionsand mineralogical and particle-size effects inherent in the use of pressed rock-powder pellets in the analytical procedure of the MTU laboratory. Other, but as yet unknown, differences in sample preparation and/or analytical technique may also be important; effects related to natural sample inhomogeneityare believed to be insignificant. The inter-laboratory differences in the analytical data complicated accurate assessment of whether El Chichón magmas have changed composition during the past 300 000 a. Knowledge of such change is needed for understanding petrogenetic history and for such related studies as evaluation of volcanic hazards.

Applied Geochemistry

Crater lake and post-eruption hydrothermal activity, El Chichón Volcano, Mexico

Explosive eruptions of Volcán El Chichón in Chiapas, Mexico on March 28 and April 3–4, 1982 removed 0.2 km 3 of rock to form a 1-km-wide 300-m-deep summit crater. By late April 1982 a lake had begun to form on the crater floor, and by November 1982 it attained a maximum surface area of 1.4 × 10 5 m 2 and a volume of 5 × 10 6 m 3 . Accumulation of 4–5 m of rainfall between July and October 1982 largely formed the lake. In January 1983, temperatures of fumaroles on the crater floor and lower crater walls ranged from 98 to 115°C; by October 1983 the maximum temperature of fumarole emissions was 99°C. In January 1983 fumarole gas emissions were greater than 99 vol. % H 2 O with traces of CO 2 , SO 2 , and H 2 S. The water of the lake was a hot ( T = 52–58°C), acidic (pH = 0.5), dilute solution (34,046 mg L −1 dissolved solids; Cl/S = 20.5). Sediment from the lake contains the same silicate minerals as the rocks of the 1982 pyroclastic deposits, together with less than 1% of elemental sulfur. The composition and temperature of the lake water is attributed to: (1) solution of fumarole emissions; (2) reaction of lake water with hot rocks beneath the lake level; (3) sediments washed into the lake from the crater walls; (4) hydrothermal fluids leaching sediments and formational waters in sedimentary rocks of the basement; (5) evaporation; and (6) precipitation.

Journal of Volcanology and Geothermal Research

Holocene eruptive activity of El Chichón Volcano, Chiapas, Mexico

Geologic and radiometric-age data indicate that El Chichón was frequently and violently active during the Holocene, including eruptive episodes about 600, 1250, and 1700 years ago and several undated, older eruptions. These episodes, involving explosive eruptions of sulfur-rich magma and associated dome-growth processes, were apparently separated by intervals of approximately 350 to 650 years. Some of El Chichón's eruptions may correlate with unusual atmospheric phenomena around A.D. 1300 and possibly A.D. 623.

Science