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Geology topics

James E. P. Utley

Publications and source records attributed to James E. P. Utley.

2 recordsLinked to original sources

Nanoscale silicate melt textures determine volcanic ash surface chemistry

Explosive volcanic eruptions produce vast quantities of silicate ash, whose surfaces are subsequently altered during atmospheric transit. These altered surfaces mediate environmental interactions, including atmospheric ice nucleation, and toxic effects in biota. A lack of knowledge of the initial, pre-altered ash surface has required previous studies to assume that the ash surface composition created during magmatic fragmentation is equivalent to the bulk particle assemblage. Here we examine ash particles generated by controlled fragmentation of andesite and find that fragmentation generates ash particles with substantial differences in surface chemistry. We attribute this disparity to observations of nanoscale melt heterogeneities, in which Fe-rich nanophases in the magmatic melt deflect and blunt fractures, thereby focusing fracture propagation within aureoles of single-phase melt formed during diffusion-limited growth of crystals. In this manner, we argue that commonly observed pre-eruptive microtextures caused by disequilibrium crystallisation and/or melt unmixing can modify fracture propagation and generate primary discrepancies in ash surface chemistry, an essential consideration for understanding the cascading consequences of reactive ash surfaces in various environments.

Nature Communications

Phase equilibrium of a high-SiO2, andesite at fO2 = RRO: Implications for Augustine volcano and other high-fO2 arc andesites

Understanding the impact of magmatic plumbing systems on explosive volcanic activity is important for hazard management. This study describes phase equilibria experiments using a high-silica andesite (HSA; SiO 2 = 62.5 wt%) from the 2006 eruption of Augustine Volcano, Alaska. Experiments were conducted under H 2 O saturated conditions, f 0 2 "> f 0 2 f02 = RRO (Re–ReO 2 or ~ Ni–NiO + 2), at pressures of 50–200 MPa ( P Total = P H2O ), and at temperatures of 800–1060 ° C. Run durations varied from 23 to 539 h, inversely scaled with temperature. The natural Augustine HSA phase assemblage (plagioclase, two pyroxenes, Fe–Ti oxides, magnesio-hornblende) was reproduced at 860–880 ° C and 120–200 MPa. Comparing experimental and natural glass and plagioclase compositions further refined those conditions to ~ 870 °C and 120–170 MPa. Crystallization of euhedral quartz was accompanied by biotite and small amounts of cummingtonite at T ≤ 850 °C. The relatively high temperature appearance of these typically low- T phases indicates that higher f 0 2 "> f 0 2 f02 could enhance their stability. The storage conditions estimated from our experiments compare well with previous magma plumbing system models for Augustine from geophysical and petrological data. The refined experimental pressure range suggests a storage depth of 4.6–6.6 km, assuming a crustal density of 2650 kg/m 3 . The strong petrological and geochemical similarities between the products of the 2006, 1986, and 1976 eruptions suggest that the Augustine magmatic system had generally consistent crystallization conditions for the HSA lithology during that > 30-year time interval. The experimental results broad implications for understanding higher f 0 2 "> f 0 2 magmas at andesitic arc volcanoes.

Alaska