Nagasaki, Shiho, Ishibashi, Hidemi, Suwa, Yukiko, Yasuda, Atsushi, Hokanishi, Natsumi, Ohkura, Takahiro, and Takemura, Keiji
Calcic amphibole phenocrysts in the Tsurumidake summit (TS) lava, which was produced during the most recent eruption at Tsurumi Volcano (SW Japan) at around 7.5–10.5 ka, have been analyzed to determine the pre-eruptive conditions, such as temperature ( T ), pressure ( P ), oxygen fugacity ( f O 2 ), SiO 2 content (SiO 2 melt ), and FeO*/MgO ratio (FeO*/MgO melt ), of coexisting silicate melts in the magma reservoir beneath the volcano. Although most of the amphibole phenocrysts have been completely decomposed to a fine-grained opaque symplectite, ~ 6% of the grains remain intact. The degree of amphibole breakdown (DAB), defined as the ratio of the area of symplectite to the area of symplectite plus relict amphibole in each phenocryst, varies from ~ 20% to 100%. Compositional zoning was not observed in the amphibole grains, however, two distinct groups of amphibole phenocrysts have been identified based on their chemical compositions: group-I amphiboles, which are relatively Si-poor, and [6] Al-rich, and have a relatively high Mg# [100Mg/(Mg + Fe 2 + )]; and group-II amphiboles, which are Si-rich, and [6] Al-poor, and have a relatively low Mg#. Empirical equations for geothermobarometry, oxygen barometry and chemometry that exclusively rely on the amphibole composition were applied to estimate the T – P – f O 2 –SiO 2 melt –FeO*/MgO melt conditions of the silicate melts with which the amphibole crystals equilibrated. The results show that group-I and group-II amphiboles equilibrated with andesitic melts (group-I melts) and dacitic–rhyolitic melts (group-II melts), respectively. The T – P – f O 2 conditions of group-I melts were estimated as ~ 374–483 MPa (~ 13.9–17.9 km depth), ~ 950 °C, and NNO + 1.3, respectively, and those of group-II melts were ~ 93–242 MPa (~ 3.4–9.0 km depth), 824–913 °C, and NNO + 0.6–1.7, respectively. The estimated T – P – f O 2 –SiO 2 melt –FeO*/MgO melt conditions were almost constant for group-I melts, whereas the T , Δ NNO , and FeO*/MgO melt values of group-II melts decreased with increasing SiO 2 melt . The DAB decreased as the temperature increased; low-DAB grains are absent in group-II amphiboles. Our results suggest that (1) a deeper reservoir (at a depth of ~ 16 km) stored an andesitic melt coexisting with group-I amphiboles at ~ 950 °C; (2) a chemically zoned reservoir at shallower depth (~ 6.4 km) was filled with dacitic–rhyolitic melts that coexisted with group-II amphiboles at ~ 824–913 °C; (3) the TS lava was the product of magma mixing of at least three components, including the andesitic melt derived from the deeper reservoir, the dacitic and rhyolitic melts from the shallower reservoir and a mafic magma derived from the lower crust and/or upper mantle; and (4) the TS lava eruption occurred within a month or less of the magma mixing. [ABSTRACT FROM AUTHOR]