Abstract
The most recent and largest caldera-forming eruption occurred at ~ 90 ka at Aso Volcano, SW Japan, and is known as the “Aso-4 eruption.” We performed chemical analyses of amphibole phenocrysts from Aso-4 pyroclasts collected from the initial and largest pyroclastic unit (4I-1) of the eruption to infer the composition–temperature–pressure conditions of the melt that crystallized amphibole phenocrysts. Each amphibole phenocryst is largely chemically homogeneous, but inter-grain chemical variation is observed. Geothermometry, geobarometry, and melt–SiO2 relationships based on amphibole single-phase compositions reveal that most amphibole phenocrysts were in equilibrium with hydrous melt comprising ~ 63–69 wt% SiO2 ({text{SiO}}_{2}^{text{melt}}) at 910–950 °C, although several grains were crystallized from more mafic and higher-temperature melts (~ 57–60.5 wt% SiO2 and 965–980 °C). The amphibole temperatures are comparable with those previously estimated from two-pyroxene geothermometry, but are much higher than temperatures previously estimated from Fe–Ti oxide geothermometry. The estimated {text{SiO}}_{2}^{text{melt}} contents are lower than that of the host melt in the 4I-1 pyroclasts. Chemical and thermal disequilibrium between the amphibole rims and the host melt, as well as intra-grain homogeneity and inter-grain heterogeneity of amphibole compositions, suggests that these amphiboles were incorporated into the host melt immediately prior to the caldera-forming eruption. Our results suggest that the amphibole phenocrysts, and perhaps some of the pyroxene and plagioclase phenocrysts, were derived from a chemically and thermally zoned crystal mush layer that had accumulated beneath the chamber of the host 4I-I melt. Amphibole geobarometry indicates a crystallization depth of ~ 13.9 ± 3.5 km, which is consistent with the present-day magma chamber depth beneath the volcano as inferred from geophysical observations. The results suggest that the depth of the post-caldera magma plumbing system is strongly influenced by a relic magma reservoir related to a previous caldera-forming eruption.
Highlights
Caldera-forming eruptions are the most violent and catastrophic volcanic phenomena and have a significant influence on the surface environment on a global scale (e.g., Miller and Wark 2008; Druitt et al 2012)
Texture and compositions of amphibole phenocrysts Aso-4 ejecta are crystal-poor with a modal abundance of phenocrysts of 5–10 vol%, with the exception of scoriae with 10–37 vol% of phenocrysts (Kaneko et al 2007)
Amphibole phenocrysts are euhedral with rare breakdown rims (Fig. 2a–c)
Summary
Caldera-forming eruptions are the most violent and catastrophic volcanic phenomena and have a significant influence on the surface environment on a global scale (e.g., Miller and Wark 2008; Druitt et al 2012). It is critical to understand the causes and processes of caldera-forming eruptions To address this issue, quantifying the pre-eruptive physicochemical conditions of Igneous amphibole has been the focus of many recent studies (e.g., De Angelis et al 2013; Shane and Smith 2013; Erdmann et al 2014; Kiss et al 2014). The T, P, and SiOm2 elt related to amphibole crystallization can be estimated without assuming equilibrium between phases. Empirical thermobarometric and chemometric equations based on a single-phase composition of amphibole are valuable because they do not assume inter-phase equilibrium (Putirka 2016) and are useful in detecting phase disequilibrium between amphibole and other phases. The detection of phase disequilibrium in magma is essential in reconstructing the pre-eruptive processes of caldera-forming eruptions based on petrological information recorded in pyroclasts
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