Abstract A Robust tectonic reconstruction of the Philippine Sea Plate around ∼52 Ma is a prerequisite in understanding the process of subduction initiation and establishment of the Izu‐Bonin‐Mariana arc. This study investigates origins and timing of basin formation in the still poorly understood oldest part of the northern Philippine Sea plate. We have established that andesitic magmatism in the form of the Northern Philippine Sea volcanics is widely distributed across this area. It is founded on both a Mesozoic arc terrane (Daito Ridge Group) and an intervening basin (Kita‐Daito Basin). Their narrow Eocene age range (45‐41 Ma) and lack of systematic spatial variation in geochemistry implies that this magmatism was not associated with on‐going subduction, but related to the rifting/spreading event forming the Kita‐Daito Basin. The arc‐like geochemistry of the volcanics seems to indicate melting of lithospheric mantle which had been previously metasomatized by Mesozoic subduction of a plate with Pacific‐MORB isotopic characteristics. Late Eocene basaltic magmatism also found in the Kita‐Daito Basin does not have arc‐like characteristics, and could have formed from low‐degree melts of asthenospheric mantle associated with the final stage of Kita‐Daito Basin spreading. As onset of activity of the Northern Philippine Sea volcanics is essentially synchronous with the magmatism associated with the Oki‐Daito mantle plume, it is possible that both magmatism and rifting of the Kita‐Daito Basin were triggered by the arrival of the Oki‐Daito mantle plume in this region. These results demonstrate that the Kita‐Daito Basin postdates subduction initiation of the Pacific Plate along the Izu‐Bonin‐Mariana arc.
Abstract Glaciovolcanic deposits at Tongariro and Ruapehu volcanoes, New Zealand, represent diverse styles of interaction between wet-based glaciers and andesitic lava. There are iceconfined lavas, and also hydroclastic breccia and subaqueous pyroclastic deposits that formed during effusive and explosive eruptions into meltwater beneath the glacier; they are rare among globally reported products of andesitic glaciovolcanism. The apparent lack of hydrovolcanically fragmented andesite at ice-capped volcanoes has been attributed to a lack of meltwater at the interaction sites because either the thermal characteristics of andesite limit meltwater production or meltwater drains out through leaky glaciers and down steep volcano slopes. We used published field evidence and novel, dynamic andesite-ice experiments to show that, in some cases, meltwater accumulates under glaciers on andesitic volcanoes and that meltwater production rates increase as andesite pushes against an ice wall. We concur with models for eruptions beneath ice sheets showing that the glacial conditions and pre-eruption edifice morphology are more important controls on the style of glaciovolcanism and its products than magma composition and the thermal properties of magmas. Glaciovolcanic products can be useful proxies for paleoenvironment, and the range of andesitic products and the hydrological environments in which andesite erupts are greater than hitherto appreciated.
Abstract Cristobalite is a low-pressure, high-temperature SiO2 polymorph that occurs as a metastable phase in many geologic settings, including as crystals deposited from vapor within the pores of volcanic rocks. Such vapor-phase cristobalite (VPC) has been inferred to result from silica redistribution by acidic volcanic gases but a precise mechanism for its formation has not been established. We address this by investigating the composition and structure of VPC deposited on plagioclase substrates within a rhyolite lava flow, at the micrometer to nanometer scale. The VPC contains impurities of the form [AlO4/Na+]0—coupled substitution of Al3+ charge-balanced by interstitial Na+—which are typical of cristobalite. However, new electron probe microanalysis (EPMA) element maps show individual crystals to have impurity concentrations that systematically decline from crystal cores-to-rims, and atom probe tomography reveals localized segregation of impurities to dislocations. Impurity concentrations are inversely correlated with degrees of crystallinity [observed by electron backscatter diffraction (EBSD), hyperspectral cathodoluminescence, laser Raman, and transmission electron microscopy (TEM)], such that crystal cores are poorly crystalline and rims are highly ordered tetragonal α-cristobalite. The VPC-plagioclase interfaces show evidence that dissolution-reprecipitation reactions between acidic gases and plagioclase crystals yield precursory amorphous SiO2 coatings that are suitable substrates for initial deposition of impure cristobalite. Successive layers of cubic β-cristobalite are deposited with impurity concentrations that decline as Al-bearing gases rapidly become unstable in the vapor cooling within pores. Final cooling to ambient temperature causes a displacive transformation from β→α cristobalite, but with locally expanded unit cells where impurities are abundant. We interpret this mechanism of VPC deposition to be a natural proxy for dopant-modulated Chemical Vapor Deposition, where halogen-rich acidic gases uptake silica, react with plagioclase surfaces to form suitable substrates and then deposit SiO2 as impure cristobalite. Our results have implications for volcanic hazards, as it has been established that the toxicity of crystalline silica is positively correlated with its purity. Furthermore, we note that VPC commonly goes unreported, but has been observed in silicic lavas of virtually all compositions and eruptive settings. We therefore suggest that despite being metastable at Earth's surface, cristobalite may be the most widely occurring SiO2 polymorph in extrusive volcanic rocks and a useful indicator of gas-solid reaction having occurred in cooling magma bodies.
Time–composition relationships in eruptive sequences at composite volcanoes can show how the ongoing intrusion of magmas progressively affects the lithosphere at continental convergent margins. Here, new whole-rock and microanalytical major and trace element data from andesite-dacite lava flows are integrated with previous studies and existing isotopic data, and placed within the framework of a high-resolution chronostratigraphy for Ruapehu volcano (southern Taupo Volcanic Zone, New Zealand). The geochemical evolution of lavas erupted over the ~200 kyr lifetime of the exposed edifice reflects variable degrees of fractionation and systematic changes in the type of crustal assimilation in the Ruapehu magma system. Lavas erupted from ~200–150 ka have previously been distinguished from those erupted <150 ka based on Sr-Nd isotopic characteristics, which indicate that the oldest lavas were sourced from magmas that assimilated oceanic crust. Such source rocks underlie the regionally widespread Mesozoic meta-sedimentary greywacke-argillite basement, which was conversely assimilated by <150 ka magmas. New results from this work reveal that since 150 ka, an upper limit of magma differentiation occurred from ~50–35 ka. High K2O (~6 wt%) and Rb contents (~270 ppm) in melt inclusions, interstitial glass, and glass from in situ quenched melts of partially fused crustal xenoliths are reported for andesite-dacite lavas erupted during this period. In addition to crystal fractionation, selective partial melting and assimilation of K- and Rb-rich mineral phases (e.g., biotite, K-feldspar) that are significant components of the meta-sedimentary basement rocks is inferred to explain these geochemical characteristics. These processes coincided also with the effusion of high-MgO andesite-dacite lavas that display petrological evidence for mixing between andesite-dacite and more mafic magmas. An influx of hotter mafic magma into the system explains why the extent of crustal assimilation recorded by Ruapehu lavas peaked during the ~50–35 ka eruptive period. From 26 ka to the present, andesite lavas have reverted to more mafic compositions with less potassic melt inclusion and whole-rock compositions when compared to the ~50–35 ka lavas. We suggest that the younger lavas assimilated less-enriched melts because fertile phases had been preferentially extracted from the crustal column during earlier magmatism. This scenario of bottom-up heating of the lithosphere and exhaustion of fertile phases due to the progressive intrusion of magma explains the geochemical evolution of Ruapehu lavas. This model may be applicable to other long-lived composite volcanoes of the circum-Pacific continental arcs.
Abstract Dating young lava flows is essential for understanding volcano's eruption frequency, yet challenging due to methodological limitations of commonly used dating techniques. Ruapehu (Aotearoa New Zealand) produced many lava flows during the Holocene, but constraints on the timing of these eruptions are scarce. Here, we use paleomagnetic dating to deliver new eruption ages of 18 lava flows with uncertainties ranging between 500 and 2,700 years (at the 95% confidence level). Comparison between lava flows' paleomagnetic directions and a local paleosecular variation record indicates that the large lava flow field located on the Whakapapa area was emplaced during at least three distinct eruptive episodes between 10600 and 7400 BP. Two of these episodes closely followed a large collapse event that affected Ruapehu's northern area and generated large volumes of lava between 10600 and 8800 BP, with the third episode producing less voluminous lava flows between 8100 and 7400 BP. Following a smaller collapse of the southeastern sector of the edifice at ca. 5300 BP, several low‐volume lava flows were emplaced during at least two distinct eruptive episodes prior to ca. 1000 BP, which supplied the Whangaehu valley with lava. The youngest age inferred from our data represents the youngest eruption age provided for a lava flow outside Ruapehu's summit region. This research provides greater detail to the Holocene effusive chronology at Ruapehu, shedding light on partial cone reconstructions after edifice collapses during the Holocene, and the time relationships between trends observed in its effusive and explosive activity.
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