Geology topics

William I. Rose

Publications and source records attributed to William I. Rose.

At least 19 recordsLinked to original sources

USGS2012

Sulfur dioxide and particles in quiescent volcanic plumes from Poás, Arenal, and Colima Volcanos, Costa Rica and Mexico

Measurements of SO 2 emission rates and concentrations and of particle distribution, size, shape, and composition were made in quiescent volcanic plumes emitted into the troposphere from Poás and Arenal volcanos, Costa Rica, and Colima volcano, Mexico. SO 2 emission rates were 700±180 metric tons per day (t/d) for Poás, 210±30 t/d for Arenal, and 320±50 t/d for Colima. The concentrations of SO 2 calculated from the COSPEC/lidar data were 5–380 ppb. Concentrations of SO 2 measured directly by flame photometry were 10–250 ppb. Particles collected in the plumes with a quartz crystal microbalance impactor were mostly less than 3 μm in diameter and consisted of droplets of dilute sulfur-bearing solutions and minor amounts of larger silicate particles coated with a sulfur-bearing film or crust. Total particle concentrations were 4.7 μg/m 3 for Poás and 18.8 μg/m 3 for Colima. Comparison of concentrations of SO 2 in the plumes with gas samples collected at fumaroles on the ground suggests that the plumes are diluted by the atmosphere by factors of up to 10 5 .

Journal of Geophysical Research Atmospheres↗

USGS2009

Hydrometeor-enhanced tephra sedimentation: Constraints from the 18 May 1980 eruption of Mount St. Helens

Uncertainty remains on the origin of distal mass deposition maxima observed in many recent tephra fall deposits. In this study the link between ash aggregation and the formation of distal mass deposition maxima is investigated through reanalysis of tephra fallout from the Mount St. Helens 18 May 1980 (MSH80) eruption. In addition, we collate all the data needed to model distal ash sedimentation from the MSH80 eruption cloud. Four particle size subpopulations were present in distal fallout with modes at 2.2 Φ, 4.2 Φ, 5.9 Φ, and 8.3 Φ. Settling rates of the coarsest subpopulation closely matched predicted single‐particle terminal fall velocities. Sedimentation of particles <100 μ m was greatly enhanced, predominantly through aggregation of a particle subpopulation with modal diameter 5.9 ± 0.2 Φ (19 ± 3 μ m). Mammatus on the MSH80 cloud provided a mechanism to transport very fine ash particles, with predicted atmospheric lifetimes of days to weeks, from the upper troposphere to the surface in a matter of hours. In this mechanism, ash particles initiate ice hydrometeor formation high in the troposphere. Subsequently, the volcanic cloud rapidly subsides as mammatus develop from increased particle loading and cloud base sublimation. Rapid fallout occurs as the cloud passes through the melting level in a process analogous to snowflake aggregation. Aggregates sediment en masse and form the distal mass deposition maxima observed in many recent volcanic ash fall deposits. This work provides a data resource that will facilitate tephra sedimentation modeling and allow model intercomparisons.

Washington↗

USGS2006

Atmospheric chemistry of a 33-34 hour old volcanic cloud from Hekla Volcano (Iceland): Insights from direct sampling and the application of chemical box modeling

On 28 February 2000, a volcanic cloud from Hekla volcano, Iceland, was serendipitously sampled by a DC-8 research aircraft during the SAGE III Ozone Loss and Validation Experiment (SOLVE I). It was encountered at night at 10.4 km above sea level (in the lower stratosphere) and 33-34 hours after emission. The cloud is readily identified by abundant SO2 (???1 ppmv), HCl (???70 ppbv), HF (???60 ppbv), and particles (which may have included fine silicate ash). We compare observed and modeled cloud compositions to understand its chemical evolution. Abundances of sulfur and halogen species indicate some oxidation of sulfur gases but limited scavenging and removal of halides. Chemical modeling suggests that cloud concentrations of water vapor and nitric acid promoted polar stratospheric cloud (PSC) formation at 201-203 K, yielding ice, nitric acid trihydrate (NAT), sulfuric acid tetrahydrate (SAT), and liquid ternary solution H2SO4/H2O/HNO3 (STS) particles. We show that these volcanically induced PSCs, especially the ice and NAT particles, activated volcanogenic halogens in the cloud producing >2 ppbv ClOx. This would have destroyed ozone during an earlier period of daylight, consistent with the very low levels of ozone observed. This combination of volcanogenic PSCs and chlorine destroyed ozone at much faster rates than other PSCs that Arctic winter. Elevated levels of HNO3 and NOy in the cloud can be explained by atmospheric nitrogen fixation in the eruption column due to high temperatures and/or volcanic lightning. However, observed elevated levels of HOx remain unexplained given that the cloud was sampled at night. Copyright 2006 by the American Geophysical Union.

Journal of Geophysical Research D: Atmospheres↗

USGS2006

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↗

USGS2006

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↗

USGS2005

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↗

USGS2001

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↗

USGS1999

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↗

USGS1999

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↗

USGS1990

Evaluation of gases, condensates, and SO2 emissions from Augustine volcano, Alaska: the degassing of a Cl-rich volcanic system

After the March-April 1986 explosive eruption a comprehensive gas study at Augustine was undertaken in the summers of 1986 and 1987. Airborne COSPEC measurements indicate that passive SO2 emission rates declined exponentially during this period from 380??45 metric tons/day (T/D) on 7/24/86 to 27??6 T/D on 8/24/87. These data are consistent with the hypothesis that the Augustine magma reservoir has become more degassed as volcanic activity decreased after the spring 1986 eruption. Gas samples collected in 1987 from an 870??C fumarole on the andesitic lava dome show various degrees of disequilibrium due to oxidation of reduced gas species and condensation (and loss) of H2O in the intake tube of the sampling apparatus. Thermochemical restoration of the data permits removal of these effects to infer an equilibrium composition of the gases. Although not conclusive, this restoration is consistent with the idea that the gases were in equilibrium at 870??C with an oxygen fugacity near the Ni-NiO buffer. These restored gas compositions show that, relative to other convergent plate volcanoes, the Augustine gases are very HCl rich (5.3-6.0 mol% HCl), S rich (7.1 mol% total S), and H2O poor (83.9-84.8 mol% H2O). Values of ??D and ??18O suggest that the H2O in the dome gases is a mixture of primary magmatic water (PMW) and local seawater. Part of the Cl in the Augustine volcanic gases probably comes from this shallow seawater source. Additional Cl may come from subducted oceanic crust because data by Johnston (1978) show that Cl-rich glass inclusions in olivine crystals contain hornblende, which is evidence for a deep source (>25km) for part of the Cl. Gas samples collected in 1986 from 390??-642??C fumaroles on a ramp surrounding the inner summit crater have been oxidized so severely that restoration to an equilibrium composition is not possible. H and O isotope data suggest that these gases are variable mixtures of seawater, FMW, and meteoric steam. These samples are much more H2O-rich (92%-97% H2O) than the dome gases, possibly due to a larger meteoric steam component. The 1986 samples also have higher Cl/S, S/C, and F/Cl ratios, which imply that the magmatic component in these gases is from the more degassed 1976 magma. Thus, the 1987 samples from the lava dome are better indicators than the 1986 samples of degassing within the Augustine magma reservoir, even though they were collected a year later and contain a significant seawater component. Future gas studies at Augustine should emphasize fumaroles on active lava domes. Condensates collected from the same lava-dome fumarole have enrichments ot 107-102 in Cl, Br, F, B, Cd, As, S, Bi, Pb, Sb, Mo, Zn, Cu, K, Li, Na, Si, and Ni. Lower-temperature (200??-650??C) fumaroles around the volcano are generally less enriched in highly volatile elements. However, these lower-termperature fumaroles have higher concentration of rock-forming elements, probably derived from the wall rock. ?? 1990 Springer-Verlag.

Bulletin of Volcanology↗

USGS1989

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↗

USGS1988

Detailed record of SO2 emissions from Pu'u `O`o between episodes 33 and 34 of the 1983-86 ERZ eruption, Kilauea, Hawaii

A tripod-mounted correlation spectrometer was used to measure SO2 emissions from Pu`u `O`o vent, mid-ERZ, Kilauea, Hawaii between Episodes 33 and 34 (June 13 to July 6, 1985). In 24 repose days, 906 measurements were collected, averaging 38 determinations/day. Measurements reflect 13% of the total 576 hours of the repose and 42% of the bright daylight hours. The average SO2 emission for the 24-day repose interval is 167??83 t/d, a total of 4000 tonnes emitted for the entire repose. The large standard deviation reflects the "puffing" character of the plume. The overall rate of SO2 degassing gently decreased with a zero-intercept of 44-58 days and was interrupted by two positive peaks. The data are consistent with the gas emanating from a cylindrical conduit of 50 meter diameter and a length of 1700 meters which degasses about 50% of its SO2 during 24 days. This is in support of the Pu'u `O`o model of Greenland et al. (1987). 36 hours before the onset of Episode 34 (July 5-6, 1985), elevated SO2 emissions were detected while the magma column was extremely active ultimately spilling over during dome fountaining. A "mid-repose" anomaly of SO2 emission (June 21-22, 1985) occurs two days before a sudden increase in the rate of summit inflation (on June 24, 1985), suggesting magma was simultaneously being injected in both the ERZ and summit reservoir until July 24 when it was channelled only to the summit reservoir. This implies degassing magma is sensitive to perturbations within the rift zone conduit system and may at times reflect these disturbances. Periods of 7-45 min are detected in the daily SO2 emissions, which possibly reflect timing of convective overturn in the cylindrical magma body. If the 33-34 repose interval is considered representative of other repose periods, the ERZ reposes of Jan 1983-Jan 1986 ERZ activity, contributed 1.6 ?? 105 tonnes of SO2 to the atmosphere. Including summit fuming from non-eruptive fumaroles (2.7 ?? 105 tonnes SO2); 28% of the total SO2 budget from Kilauea between Jan 1983 to Jan 1986 was contributed by quiescent degassing, and the remainder was released during explosive fountaining episodes. ?? 1988 Springer-Verlag.

Bulletin of Volcanology↗

USGS1987

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↗

USGS1987

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↗

USGS1987

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↗

USGS1985

An estimate of gas emissions and magmatic gas content from Kilauea volcano

Emission rates of CO 2 have been measured at Kilauea volcano, Hawaii, in the east-rift eruptive plume and CO 2 and SO 2 have been measured in the plume from the noneruptive fumaroles in the summit caldera. These data yield an estimate of the loading of Kilauean eruptive gases to the atmosphere and suggest that such estimates may be inferred directly from measured lava volumes. These data, combined with other chemical and geologic data, suggest that magma arrives at the shallow summit reservoir containing (wt.%) 0.32% H 2 O, 0.32% CO 2 and 0.09% S. Magma is rapidly degassed of most of its CO 2 in the shallow reservoir before transport to the eruption site. Because this summit degassing yields a magma saturated and in equilibrium with volatile species and because transport of the magma to the eruption site occurs in a zone no shallower than the summit reservoir, we suggest that eruptive gases from Kilauea characteristically should be one of two types: a ‘primary’ gas from fresh magma derived directly from the mantle and a carbon-depleted gas from magma stored in the summit reservoir.

Geochimica et Cosmochimica Acta↗

USGS1984

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↗

USGS1984

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↗