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57 records · Page 4Linked to original sources

Magmatic gas scrubbing: Implications for volcano monitoring

Despite the abundance of SO2(g) in magmatic gases, precursory increases in magmatic SO2(g) are not always observed prior to volcanic eruption, probably because many terrestrial volcanoes contain abundant groundwater or surface water that scrubs magmatic gases until a dry pathway to the atmosphere is established. To better understand scrubbing and its implications for volcano monitoring, we model thermochemically the reaction of magmatic gases with water. First, we inject a 915??C magmatic gas from Merapi volcano into 25??C air-saturated water (ASW) over a wide range of gas/water mass ratios from 0.0002 to 100 and at a total pressure of 0.1 MPa. Then we model closed-system cooling of the magmatic gas, magmatic gas-ASW mixing at 5.0 MPa, runs with varied temperature and composition of the ASW, a case with a wide range of magmatic-gas compositions, and a reaction of a magmatic gas-ASW mixture with rock. The modeling predicts gas and water compositions, and, in one case, alteration assemblages for a wide range of scrubbing conditions; these results can be compared directly with samples from degassing volcanoes. The modeling suggests that CO2(g) is the main species to monitor when scrubbing exists; another candidate is H2S(g), but it can be affected by reactions with aqueous ferrous iron. In contrast, scrubbing by water will prevent significant SO2(g) and most HCl(g) emissions until dry pathways are established, except for moderate HCl(g) degassing from pH < 0.5 hydrothermal waters. Furthermore, it appears that scrubbing will prevent much, if any, SO2(g) degassing from long-resident boiling hydrothermal systems. Several processes can also decrease or increase H2(g) emissions during scrubbing making H2(g) a poor choice to detect changes in magma degassing. We applied the model results to interpret field observations and emission rate data from four eruptions: (1) Crater Peak on Mount Spurr (1992) where, except for a short post-eruptive period, scrubbing appears to have drastically diminished pre-, inter-, and post-eruptive SO2(g) emissions, but had much less impact on CO2(g) emissions. (2) Mount St. Helens where scrubbing of SO2(g) was important prior to and three weeks after the 18 May 1980 eruption. Scrubbing was also active during a period of unrest in the summer of 1998. (3) Mount Pinatubo where early drying out prevented SO2(g) scrubbing before the climactic 15 June 1991 eruption. (4) The ongoing eruption at Popocate??petl in an arid region of Mexico where there is little evidence of scrubbing. In most eruptive cycles, the impact of scrubbing will be greater during pre- and post-eruptive periods than during the main eruptive and intense passive degassing stages. Therefore, we recommend monitoring the following gases: CO2(g) and H2S(g) in precursory stages; CO2(g), H2S(g), SO2(g), HCl(g), and HF(g) in eruptive and intense passive degassing stages; and CO2(g) and H2S(g) again in the declining stages. CO2(g) is clearly the main candidate for early emission rate monitoring, although significant early increases in the intensity and geographic distribution of H2S(g) emissions should be taken as an important sign of volcanic unrest and a potential precursor. Owing to the difficulty of extracting SO2(g) from hydrothermal waters, the emergence of > 100 t/d (tons per day) of SO2(g) in addition to CO2(g) and H2S(g) should be taken as a criterion of magma intrusion. Finally, the modeling suggests that the interpretation of gas-ratio data requires a case-by-case evaluation since ratio changes can often be produced by several mechanisms; nevertheless, several gas ratios may provide useful indices for monitoring the drying out of gas pathways. Published by Elsevier Science B.V.

Journal of Volcanology and Geothermal Research↗

Mount St. Augustine volcano fumarole wall rock alteration: Mineralogy, zoning, composition and numerical models of its formation process

Intensely altered wall rock was collected from high-temperature (640 °C) and low-temperature (375 °C) vents at Augustine volcano in July 1989. The high-temperature altered rock exhibits distinct mineral zoning differentiated by color bands. In order of decreasing temperature, the color bands and their mineral assemblages are: (a) white to grey (tridymite-anhydrite); (b) pink to red (tridymite-hematite-Fe hydroxide-molysite (FeCl 3 ) with minor amounts of anhydrite and halite); and (c) dark green to green (anhydrite-halite-sylvite-tridymite with minor amounts of molysite, soda and potash alum, and other sodium and potassium sulfates). The alteration products around the low-temperature vents are dominantly cristobalite and amorphous silica with minor potash and soda alum, aphthitalite, alunogen and anhydrite. Compared to fresh 1986 Augustine lava, the altered rocks exhibit enrichments in silica, base metals, halogens and sulfur and show very strong depletions in Al in all alteration zones and in iron, alkali and alkaline earth elements in some of the alteration zones. To help understand the origins of the mineral assemblages in altered Augustine rocks, we applied the thermochemical modeling program, GASWORKS, in calculations of: (a) reaction of the 1987 and 1989 gases with wall rock at 640 and 375 °C; (b) cooling of the 1987 gas from 870 to 100 °C with and without mineral fractionation; (c) cooling of the 1989 gas from 757 to 100 °C with and without mineral fractionation; and (d) mixing of the 1987 and 1989 gases with air. The 640 °C gas-rock reaction produces an assemblage consisting of silicates (tridymite, albite, diopside, sanidine and andalusite), oxides (magnetite and hercynite) and sulfides (bornite, chalcocite, molybdenite and sphalerite). The 375 °C gas-rock reaction produces dominantly silicates (quartz, albite, andalusite, microcline, cordierite, anorthite and tremolite) and subordinate amounts of sulfides (pyrite, chalcocite and wurtzite), oxides (magnetite), sulfates (anhydrite) and halides (halite). The cooling calculations produce: (a) anhydrite, halite, sylvite; (b) Cu, Mo, Fe and Zn sulfides; (c) Mg fluoride at high temperature (> 370 °C); (d) chlorides, fluorides and sulfates of Mn, Fe, Zn, Cu and Al at intermediate temperature (170–370 °C); and (e) hydrated sulfates, liquid sulfur, crystalline sulfur, hydrated sulfuric acid and water at low temperature (< 170°C). The volcanic gas-air mixing calculation produces major amounts of Na and K sulfates, minor amounts of hematite and trace amounts (< 1%) of anhydrite at log gas/air (Ig/a) ratios > 0.41 (> 628°C). This is followed by precipitation of sulfates of Fe, Cu. Pb. Zn and Al at Ig/a ratios between 0.31 and -0.4 (>628-178°C). At a lg/r ratio of ≤ -0.4 (178°C). anhydrous sulfates are replaced by their hydrated forms and hygroscopic sulfuric acid forms. At these low g/a ratios. hydrated sulfuric acid becomes the dominant phase in the system. Comparison of the thermochemical modeling results with the natural samples suggests that the alteration assemblages include: (1) minerals that precipitate from direct cooling of the volcanic gas; (2) phases that form by volcanic gases mixing with air: and (3) phases that form by volcanic gas-air-rock reaction. A complex interplay of the three processes produces the observed mineral zoning. Another implication of the numerical simulation results is that most of the observed incrustation and sublimate minerals apparently formed below 700°C.

Journal of Volcanology and Geothermal Research↗

Seismicity and seismic structure at Okmok Volcano, Alaska

Okmok volcano is an active volcanic caldera located on the northeastern portion of Umnak Island in the Aleutian arc, with recent eruptions in 1997 and 2008. The Okmok area had ~900 locatable earthquakes between 2003 and June 2008, and an additional ~600 earthquakes from the beginning of the 2008 eruption to mid 2009, providing an adequate dataset for seismic tomography. To image the seismic velocity structure of Okmok, we apply waveform cross-correlation using bispectrum verification and double-difference tomography to a subset of these earthquakes. We also perform P-wave attenuation tomography using a spectral decay technique. We examine the spatio-temporal characteristics of seismicity in the opening sequence of the 2008 eruption to investigate the path of magma migration during the establishment of a new eruptive vent. We also incorporate the new earthquake relocations and three-dimensional (3D) velocity model with first-motion polarities to compute focal mechanisms for selected events in the 2008 pre-eruptive and eruptive periods. Through these techniques we obtain precise relocations, a well-constrained 3D P-wave velocity model, and a marginally resolved S-wave velocity model. We image a main low Vp and Vs anomaly directly under the caldera consisting of a shallow zone at 0–2 km depth connected to a larger deeper zone that extends to about 6 km depth. We find that areas of low Qp are concentrated in the central to southwestern portion of the caldera and correspond fairly well with areas of low Vp. We interpret the deeper part of the low velocity anomaly (4–6 km depth) beneath the caldera as a magma body. This is consistent with results from ambient noise tomography and suggests that previous estimates of depth to Okmok's magma chamber based only on geodetic data may be too shallow. The distribution of events preceding the 2008 eruption suggest that a combination of overpressure in the zone surrounding the magma chamber and the introduction of new material from below were jointly responsible for the explosive eruption. Magma escaping from the top of the main magma chamber likely reacted with both a smaller shallow pod of magma and groundwater on its way up below the Cone D area. The earthquakes in the 2008 pre-eruptive and eruptive periods are found to have a mixture of strike-slip, oblique normal, and oblique thrust mechanisms, with a dominant P-axis orientation that is nearly perpendicular to the regional tectonic stress. This may indicate that the stresses related to magmatic activity locally dominated regional tectonic forces during this time period.

Alaska↗