17 research outputs found

    Buoyant hydrous mantle plume from the mantle transition zone

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    Abstract Magmatism at some intraplate volcanoes and large igneous provinces (LIPs) in continental areas may originate from hydrous mantle upwelling (i.e. a plume) from the mantle transition zone (MTZ) at 410–660 km depths in the Earth’s deep interior. However, the ultimate origin of the magmatism, i.e. why mantle plumes could have been generated at the MTZ, remains unclear. Here, we study the buoyancy of a plume by investigating basalts from the Changbaishan volcano, beneath which a mantle plume from the hydrous MTZ is observed via seismology. Based on carefully determined water contents of the basalts, the potential temperature of the source mantle is estimated to be 1310–1400 °C, which is within the range of the normal upper mantle temperature. This observation suggests that the mantle plume did not have a significant excess heat, and that the plume upwelled because of buoyancy resulting from water supplied from the Pacific slab in the MTZ. Such a hydrous mantle plume can account for the formation of extremely hydrous LIP magmatism. The water was originally sourced from a stagnant slab and stored in the MTZ, and then upwelled irrespective of the presence or absence of a deep thermal plume

    Chlorine Heterogeneity in Volcanic Glass as a Faithful Record of Silicic Magma Degassing

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    Degassing processes occurring within silicic magma, such as bubble growth, bubble resorption, the welding of magma fragments, and open-system gas loss are crucial in the control of volcanic eruption and lava emplacement, yet their details are still debated. To examine the possibility that these degassing processes are recorded in volcanic glass as heterogeneous Cl distribution patterns, we experimentally simulated these processes by heating rhyolitic obsidian and analyzed the distribution of Cl content in the recovered sample. The results showed that, for bubble growth, Cl diffused toward the bubble interface, leading to Cl depletion around the bubble. For bubble resorption, Cl was discharged from the bubble to the melt, leading to Cl enrichment in the ambient melt. For welding of magma fragments, Cl was depleted near the welded interface because each fragment had degassed Cl at the surface before the welding took place. For open-system gas loss, Cl exsolved at the bubble interface while the bubble itself was being collapsed into a chain of small bubbles and a Cl-depleted tail. These results indicate that Cl distribution is a reliable record of the experienced degassing processes. We then analyzed the Cl distribution in silicic lava from Naruko volcano, Japan, to study the gas flow mechanism. We observed that the glassy matrix was progressively corroded into porous crystalline material. The interface of the glass was highly enriched in Cl. We conclude that a Cl-rich gas fluxed through hot lava and corroded the glass, developing a porous, gas-permeable region

    Controls on the Salinity of Sedimentary Basinal Fluids Under Constant Chemogravitational Potential Conditions

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    Abstract Fluids in sedimentary basins exert a crucial influence on various geological phenomena including natural resource formation. Worldwide drilling projects have revealed that the salinity of sedimentary basinal fluids generally increases with depth, irrespective of lithology, age of sediments, or the presence of a halite bed. However, how these vertical salinity variations are produced and what controls the salinity remain unclear. This work examines a new hypothesis that downward‐increasing salinity variations are a natural outcome of the constant chemogravitational potential condition. In a static environment, the salinity is distributed such that the chemogravitational potential of the solute is constant with depth. Once formed, such a distribution would be maintained because no further migration of the solute would occur. To test the hypothesis, a constant chemogravitational potential distribution model was constructed for NaCl–H2O fluids in the sediment column, and NaCl content at each depth was calculated. The results showed that NaCl content monotonically increases with depth, and the variations are similar to the trend of measured data. However, the data were not necessarily completely reproduced by the model, and deviated in some parts from the calculated profile. Such deviation may indicate fluxing of external fluid occurring in these parts, as the constant chemogravitational potential is vulnerable to an advective flow. Therefore, it is proposed that the constant chemogravitational potential condition is a possible endmember theory, influencing natural salinity variations in a static environment

    Carbonate ions in high-SiO2 rhyolite observed in fluid-melt equilibrium experiments

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    We carried out equilibrium experiments of the CO2-H2O-rhyolite system at 0.1–1.5 GPa and 850 and 1200∞C to examine the solubility and speciation of CO2 in high-SiO2 rhyolite (SiO2 > 76 wt%). We observed that both CO2 molecules (CO2mol) and carbonate anions (CO3 2–) are dissolved in the quenched rhyolitic glasses based on infrared spectroscopy. This result contrasts with the general understanding that high-SiO2 rhyolitic melt dissolves CO2mol only. The concentrations of CO2mol and CO3 2– were 199–9200 ppm and 58–2100 ppm, respectively, as quantified based on the Beer-Lambert’s law and newly determined extinction coefficients of 1192 ± 130 L·cm–1·mol–1 and 91 ± 28 L·cm–1·mol–1 for CO2mol and CO3 2–, respectively. The water content ranged from 2.6 to 6.1 wt%. Using the thermodynamic analysis, we calculated the partial molar volume of CO2mol to be VCO mol melt 2 = 24.9 ± 2.0 cm3/mol and enthalpy of dissolution to be DslnH = –22.2 ± 6.3 kJ/mol. Changes in volume and enthalpy upon the formation reaction of CO3 2– were calculated to be DrV = –8.6 ± 0.9 cm3/ mol and DrH = +1.1 ± 4.4 kJ/mol, respectively

    Pre-eruption magmatic processes and magma plumbing system at Hachijo-Nishiyama volcano, Izu–Bonin arc, Japan

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    Abstract Nishiyama volcano on Hachijojima Island is an active basaltic volcano located in the Izu–Bonin arc. In this study, petrological and geochemical analyses were conducted on mafic lavas and pyroclastics to understand the magma plumbing system and pre-eruption magmatic processes. Whole-rock major element compositions show significant variations (49.4–54.9 wt.% SiO2), and the samples contain variable amounts of plagioclase phenocrysts (1–40 vol.%). The whole-rock Sr, Nd, and Pb isotopic compositions of samples from the youngest volcanic stage (< 0.7 ka) are homogeneous, whereas some samples from the older stage (3–1 ka) have relatively low Pb isotopic ratios. This observation suggests that the younger magmas were derived from a single parental magma, but another parental magma with distinct geochemical features was involved in the magmatic system before 1 ka. The temporal variation in the FeO*/MgO ratios of the volcanic products is complex and is considered to reflect the intermittent injection of primitive magmas into the main magma chamber in which fractional crystallization occurred. Two-pyroxene geobarometry suggests that the main magma chamber was located at a depth of 9–12 km. The core region of some plagioclase phenocrysts consists of a glass inclusion-free inner core and an inclusion-rich outer mantle, suggesting that some plagioclase crystallized in the main magma chamber, which was followed by overgrowth during magma ascent because of increasing liquidus temperatures due to decompression-induced water exsolution from the melt. The whole-rock compositions of some eruption units with different Al2O3/MgO ratios exhibit distinct plagioclase-controlled trends, which negates the possibility that plagioclase accumulation occurred in a stable magma chamber. In addition, the density of plagioclase was higher than that of the melt during the magma ascent to the surface. From these observations, it is suggested that the accumulation of plagioclase phenocrysts occurred in ascending magmas as the plagioclase settled relative to the surrounding melt. The estimated depth of 9–12 km for the main magma chamber coincides with the depth range over which earthquake swarms occurred in 2002, suggesting that the magma chamber is still active, and that the earthquake swarms may reflect the injection of primitive magma into the magma chamber. Graphical Abstrac
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