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A.J.R. Kent

Publications and source records attributed to A.J.R. Kent.

3 recordsLinked to original sources

Using amphibole phenocrysts to track vapor transfer during magma crystallization and transport: An example from Mount St. Helens, Washington

In order to evaluate and further constrain models for volatile movement and vapor enrichment of magma stored at shallow levels, amphibole phenocrysts from 2004–2005 Mount St. Helens dacite were analyzed for major and selected trace elements (Li, Cu, Zn, Mn, and REE) and Li isotopes. Several recent studies have examined fluid-mobile trace element abundances in phencryst phases and melt inclusions as a means of tracking volatile movement within subvolcanic magmatic systems, and high Li contents in plagioclase phenocrysts from 1980 and 2004 Mount St. Helens dacites have been interpreted as evidence that shallow magma was fluxed by a Li-bearing vapor phase prior to eruption. In amphibole phenocrysts, Zn and Mn behave compatibly, correlating to FeO ⁎ and Al 2 O 3 , and show no systematic change with time. In contrast, Li and Cu abundances in amphibole vary by up to 3 orders of magnitude (7.6–1140 μg/g and 1.7 to 94 μg/g, respectively), and do not generally correlate with either major or trace elements. However, they do correlate moderately well ( R 2 = 0.54, >> 95% confidence) with each other and show systematic temporal variations that are opposite to those observed for plagioclase, precluding a simple 1-step diffusion model for Li enrichment. We propose a Diffusion-Crystallization Multi-Stage (DCMS) model to explain the temporal variations and co-variations of Li and Cu. In early erupted dacite (October–December 2004) profiles of Li isotopes in conjunction with measured 7 Li intensities and core-to-rim increases in Li concentration are characteristic of Li diffusion into the amphiboles, consistent with prior models of plagioclase enrichment. In amphiboles from 2005 dacite, average Li and Cu concentrations are high (∼ 260–660 μg/g and ∼ 29–45 μg/g, respectively) and in contrast to amphiboles from earlier-erupted dacite, correlate weakly with Al 2 O 3 wt.%. Amphibole Al 2 O 3 concentrations are an indicator of pressure, with high-Al amphiboles crystallizing at higher pressures, and we suggest that Li and Cu are partitioned into a fluid phase during ascent and crystallization of the magma so that amphiboles crystallizing at lower pressure have correspondingly lower Li and Cu concentrations. However, low Li and Cu in amphiboles from the dacite at the start of the eruption also require crystallization from a low Li–Cu bearing melt or residence times long enough for amphiboles to re-equilibrate with a Li–Cu depleted melt. Estimated residence times suggest that amphiboles in early dacite could have been present since the end of the 1980–1986 eruptive episode at Mount St. Helens.

Journal of Volcanology and Geothermal Research

Vapor transfer prior to the October 2004 eruption of Mount St. Helens, Washington

Dome lavas from the 2004 eruption of Mount St. Helens show elevated Li contents in plagioclase phenocrysts at the onset of dome growth in October 2004. These cannot be explained by variations in plagioclase-melt partitioning, but require elevated Li contents in coexisting melt, a fact confirmed by measurements of Li contents as high as 207 µg/g in coexisting melt inclusions. Similar Li enrichment has been observed in material erupted prior to and during the climactic May 1980 eruption, and is likewise best explained via pre-eruptive transfer of an exsolved alkali-rich vapor phase derived from deeper within the magma transport system. Unlike 1980, however, high Li samples from 2004 show no evidence of excess ( 210 Pb)/( 226 Ra), implying that measurable Li enrichments may occur despite significant differences in the timing and/or extent of magmatic degassing. Diffusion modeling shows that Li enrichment occurred within ∼1 yr before eruption, and that magma remained Li enriched until immediately before eruption and cooling. This short flux time and the very high Li contents in ash produced by phreatomagmatic activity prior to the onset of dome extrusion suggest that vapor transfer and accumulation were associated with initiation of the current eruption. Overall, observation of a high Li signature in both 1980 and 2004 dacites indicates that Li enrichment may be a relatively common phenomenon, and may prove useful for petrologic monitoring of Mount St. Helens and other silicic volcanoes. Lithium diffusion is also sufficiently rapid to constrain vapor transfer on similar time scales to short-lived radionuclides.

Geology

Intensity of quartz cathodoluminescence and trace-element content in quartz from the porphyry copper deposit at Butte, Montana

Textures of hydrothermal quartz revealed by cathodoluminescence using a scanning electron microscope (SEM-CL) reflect the physical and chemical environment of quartz formation. Variations in intensity of SEM-CL can be used to distinguish among quartz from superimposed mineralization events in a single vein. In this study, we present a technique to quantify the cathodoluminescent intensity of quartz within individual and among multiple samples to relate luminescence intensity to specific mineralizing events. This technique has been applied to plutonic quartz and three generations of hydrothermal veins at the porphyry copper deposit in Butte, Montana. Analyzed veins include early quartz-molybdenite veins with potassic alteration, pyrite-quartz veins with sericitic alteration, and Main Stage veins with intense sericitic alteration. CL intensity of quartz is diagnostic of each mineralizing event and can be used to fingerprint quartz and its fluid inclusions, isotopes, trace elements, etc., from specific mineralizing episodes. Furthermore, CL intensity increases proportional to temperature of quartz formation, such that plutonic quartz from the Butte quartz monzonite (BQM) that crystallized at temperatures near 750 ??C luminesces with the highest intensity, whereas quartz that precipitated at ???250 ??C in Main Stage veins luminesces with the least intensity. Trace-element analyses via electron microprobe and laser ablation-ICP-MS indicate that plutonic quartz and each generation of hydrothermal quartz from Butte is dominated by characteristic trace amounts of Al, P, Ti, and Fe. Thus, in addition to CL intensity, each generation of quartz can be distinguished based on its unique trace-element content. Aluminum is generally the most abundant element in all generations of quartz, typically between 50 and 200 ppm, but low-temperature, Main Stage quartz containing 400 to 3600 ppm Al is enriched by an order of magnitude relative to all other quartz generations. Phosphorous is present in abundances between 25 and 75 ppm, and P concentrations in quartz show little variation among quartz generations. Iron is the least abundant of these elements in most quartz types and is slightly enriched in CL-dark quartz in pyrite-quartz veins with sericitic alteration. Titanium is directly correlated with both temperature of quartz precipitation, and intensity of quartz luminescence, such that BQM quartz contains hundreds of ppm Ti, whereas Main Stage quartz contains less than 10 ppm Ti. Our results suggest that Ti concentration in quartz is controlled by temperature of quartz precipitation and that increased Ti concentrations in quartz may be responsible for increased CL intensities.

American Mineralogist