K–Ar geochronology of the temporal change of eruptive style in the eastern Izu peninsula, central Japan

Abstract   A recent K–Ar study elucidated that eruptive style in the eastern Izu peninsula changed from polygenetic to monogenetic volcano at 0.3–0.2 Ma. To narrow down the time of change, we determined 10 K–Ar ages on Togasayama Andesite of Amagi volcano, the youngest polygenetic volcano in the area, and Togasayama Monogenetic Volcano, one of the oldest monogenetic volcanoes in the area, which overlies a part of the Togasayama Andesite. Dating results showed that the Togasayama Andesite effused at least from 0.34 to 0.20 Ma, whereas the Togasayama Monogenetic Volcano erupted at 0.26–0.29 Ma, suggesting that the northern part of the Togasayama Andesite effused after the eruption of the Togasayama Monogenetic Volcano. Considering previous data, it is therefore inferred that change of eruptive style in the eastern Izu area occurred during the period 0.29–0.20 Ma, with considerable overlap of both polygenetic and monogenetic volcanism.     

The difference in chemical composition of the 1962 lava from miyakezima magma reservoir in Japan

Many examples of mixed magmas in banded lavas have been studied. Another type of mixed magmas or inhomogeneity of magma reservoir found in the 1962 lava flows of Miyake-zima Volcano erupted from fissures is reported.     

Groundwater-level Changes Due to Pressure Gradient Induced by Nearby Earthquakes off Izu Peninsula, 1997

Anomalous water level changes were observed at two wells associated with seismic swarm activity off Izu Peninsula on March, 1997. These are coseismic water level drops followed by gradual postseismic water level rise at the time of large earthquakes during the swarm activity. The post-seismic water level rises, which can be fitted by an exponential function with a time constant of about six hours, are explained in terms of the horizontal pressure diffusion due to the pressure gradient in the aquifer induced by the coseismic static strain.     

NanoSIMS analysis of organic carbon from the Tissint Martian meteorite: Evidence for the past existence of subsurface organic‐bearing fluids on Mars

Two petrographic settings of carbonaceous components, mainly filling open fractures and occasionally enclosed in shock‐melt veins, were found in the recently fallen Tissint Martian meteorite. The presence in shock‐melt veins and the deuterium enrichments (δD up to +1183‰) of these components clearly indicate a pristine Martian origin. The carbonaceous components are kerogen‐like, based on micro‐Raman spectra and multielemental ratios, and were probably deposited from fluids in shock‐induced fractures in the parent rock of Tissint. After precipitation of the organic matter, the rock experienced another severe shock event, producing the melt veins that encapsulated a part of the organic matter. The C isotopic compositions of the organic matter (δ¹³C = ?12.8 to ?33.1‰) are significantly lighter than Martian atmospheric CO₂ and carbonate, providing a tantalizing hint for a possible biotic process. Alternatively, the organic matter could be derived from carbonaceous chondrites, as insoluble organic matter from the latter has similar chemical and isotopic compositions. The presence of organic‐rich fluids that infiltrated rocks near the surface of Mars has significant implications for the study of Martian paleoenvironment and perhaps to search for possible ancient biological activities on Mars.     

Primary proton spectrum around the knee deduced from the emulsion-chamber data obtained at Mts. Fuji and Kanbala

We have done extensive Monte Carlo simulations using the new simulation codes of CORSIKA and COSMOS to compare with the gamma-family data obtained at Mts. Fuji (3750 m above sea level) and Kanbala (5500 m above sea level). Then, we estimated the primary proton and helium spectra around the knee energy region using a multiple-layered feed-forward neural network as a classifier of primary particle kind. The selection efficiency of proton-induced family events is estimated to be 82%. The flux value of protons at 2×10¹⁵ eV is (5.5±1.5)×10⁻¹⁴ (m⁻² s⁻¹ sr⁻¹ GeV⁻¹). The result suggests heavy-enriched primary composition around the knee region.     

Evolution processes of Ordovician–Devonian arc system in the South‐Kitakami Massif and its relevance to the Ordovician ophiolite pulse

The South Kitakami Massif is one of the oldest geological domains in Japan having Silurian strata with acidic pyroclastic rocks and Ordovician–Silurian granodiorite–tonalite basement, suggesting that it was matured enough to develop acidic volcanisms in the Silurian period. On the northern and western margin of the South Kitakami Massif, an Ordovician arc ophiolite (Hayachine–Miyamori Ophiolite) and high‐pressure and low‐temperature metamorphic rocks (Motai metamorphic rocks) exhumed sometime in the Ordovician–Devonian periods are distributed. Chronological, geological, and petrochemical studies on the Hayachine–Miyamori Ophiolite, Motai metamorphic rocks, and other early Paleozoic geological units of the South Kitakami Massif are reviewed for reconstruction of the South Kitakami arc system during Ordovician to Devonian times with supplementary new data. The reconstruction suggests a change in the convergence polarity from eastward‐ to westward‐dipping subduction sometime before the Late Devonian period. The Hayachine–Miyamori Ophiolite was developed above the eastward‐dipping subduction through three distinctive stages. Two separate stages of overriding plate extension inducing decompressional melting with minor involvement of slab‐derived fluid occurred before and after a stage of melting under strong influence of slab‐derived fluids. The first overriding plate extension took place in the back‐arc side forming a back‐arc basin. The second one took place immediately before the ophiolite exhumation and near the fore‐arc region. We postulate that the second decompressional melting was triggered by slab breakoff, which was preceded by slab rollback inducing trench‐parallel wedge mantle flow and non‐steady fluid and heat transport leaving exceptionally hydrous residual mantle. The formation history of the Hayachine–Miyamori Ophiolite implies that weaker plate coupling may provide preferential conditions for exhumation of very hydrous mantle. Very hydrous peridotites involved in arc magmatism have not yet been discovered except for in the Cambrian–Ordovician periods, suggesting its implications for global geodynamics, such as the thermal state and water circulation in the mantle.     

Interdiffusion of Mg–Fe in olivine at 1,400–1,600 °C and 1 atm total pressure

The interdiffusion coefficient of Mg–Fe in olivine (D _Mg–Fe) was obtained at 1,400–1,600 °C at the atmospheric pressure with the oxygen fugacity of 10^?3.5–10^?2 Pa using a diffusion couple technique. The D _Mg–Fe shows the anisotropy (largest along the [001] direction and smallest along the [100] direction), and its activation energy (280–320 kJ/mol) is ~80–120 kJ/mol higher than that estimated at lower temperatures. The D _Mg–Fe at temperatures of >1,400 °C can be explained by the cation-vacancy chemistry determined both by the Fe³⁺/Fe²⁺ equilibrium and by the intrinsic point defect formation with the formation enthalpy of 220–270 kJ/mol depending on the thermodynamical model for the Fe³⁺/Fe²⁺ equilibrium in olivine. The formation enthalpy of 220–270 kJ/mol for the point defect (cation vacancy) in olivine is consistent with that estimated from the Mg self-diffusion in Fe-free forsterite. The increase in the activation energy of D _Mg–Fe at >1,400 °C is thus interpreted as the result of the transition of diffusion mechanism from the transition metal extrinsic domain to the intrinsic domain at the atmospheric pressure.     

Transformation textures,mechanisms of formation of high‐pressure minerals in shock melt veins of L6 chondrites,and pressure‐temperature conditions of the shock events

Abstract— The high‐pressure polymorphs of olivine, pyroxene, and plagioclase in or adjacent to shock melt veins (SMVs) in two L6 chondrites (Sahara 98222 and Yamato 74445) were investigated to clarify the related transformation mechanisms and to estimate the pressure‐temperature conditions of the shock events. Wadsleyite and jadeite were identified in Sahara 98222. Wadsleyite, ringwoodite, majorite, akimotoite, jadeite, and lingunite (NaAlSi₃O₈‐hollandite) were identified in Yamato 74445. Wadsleyite nucleated along the grain boundaries and fractures of original olivine. The nucleation and growth of ringwoodite occurred along the grain boundaries of original olivine, and as intracrystalline ringwoodite lamellae within original olivine. The nucleation and growth of majorite took place along the grain boundaries or fractures in original enstatite. Jadeite‐containing assemblages have complicated textures containing “particle‐like,” “stringer‐like,” and “polycrystalline‐like” phases. Coexistence of lingunite and jadeite‐containing assemblages shows a vein‐like texture. We discuss these transformation mechanisms based on our textural observations and chemical composition analyses. The shock pressure and temperature conditions in the SMVs of these meteorites were also estimated based on the mineral assemblages in the SMVs and in comparison with static high‐pressure experimental results as follows: 13–16 GPa, >1900 °C for Sahara 98222 and 17–24 GPa, >2100 °C for Yamato 74445.     

Olivine-spinel geospeedometry: Analysis of diffusion-controlled Mg-Fe2+ exchange

Subsolidus Mg-Fe²⁺ exchange between olivine and spinel is governed by Mg-Fe²⁺ interdiffusion. Incomplete exchange results in Mg-Fe²⁺ heterogeneity in both olivine and spinel, which provides information on the thermal histories of the host rocks. A composite sphere model has been developed to obtain quantitative cooling rates or heating duration from the Mg-Fe²⁺ heterogeneity. The model assumes that a spherical core of spinel and a surrounding semi-infinite spherical shell of olivine interact by diffusion-controlled exchange of Mg and Fe²⁺. The differential equations describing the model are solved numerically by finite difference approximations. The numerical solution reveals that cooling rates or heating duration can be estimated from the relationship between the grain size of spinel and temperature calculated from the chemical compositions of the core of a spinel grain and of olivine far away from it. The calculated temperature is employed in place of $\text{Mg}\text{(Mg + Fe}{}^{\mathrm{2+}}\text{)}$ at the center of spinel to obtain the absolute temperature of thermal events.This olivine-spinel geospeedometer has been applied to peridotites. gabbro, and picrites from some ophiolite complexes in Japan to estimate their cooling rates. The estimated cooling rates for the peridotites range from 10^?4 to 10^?1 °C/yr, and those for the picrites from 10³ to 10⁴ °C/yr. The geospeedometer has been extended to estimate the heating duration of lherzolite xenoliths in basalt from the Ichinomegata crater, northeast Japan. The estimated heating duration of the xenoliths is less than one day.     

Anisotropy of Mg isotopic fractionation during evaporation and Mg self-diffusion of forsterite in vacuum

Evaporation of solid materials under low-pressure conditions could play important roles in chemical and isotopic fractionations in the early solar system. We have studied anisotropy of isotopic fractionation of ²⁶Mg and ²⁵Mg during kinetic evaporation of forsterite (Mg₂SiO₄), which is potentially a powerful tool to understand thermal histories of crystals in the early solar system. Ion-microprobe depth profiling revealed that the Mg isotopic zoning profiles of forsterite evaporated at 1500-1700 °C are notably differing along the a-, b-, and c-axes, which can be attributed to anisotropy in self-diffusion coefficient of Mg (D) and an isotopic fractionation factor for evaporation of Mg (α). The D and α were obtained from zoning profiles by applying the diffusion-controlled isotopic fractionation model of Wang et al. [1999. Evaporation of single crystal forsterite: Evaporation kinetics, magnesium isotope fractionation, and implications of mass-dependent isotopic fractionation of a diffusion-controlled reservoir. Geochim. Cosmochim. Acta 63(6), 953-966.].The D is largest and smallest along the a- and c-axes, respectively. The activation energy of 560-670 kJ/mol indicates that Mg diffusion at 1500-1700 °C occurred in the intrinsic diffusion regime.The α seems to be larger along the a- or c-axes than along the b-axis. The α along the a- or c-axes show weak temperature dependence. The α along all the crystallographic orientations is closer to unity than that expected from the kinetic theory of gases. These lines of evidence suggest that surface processes such as breaking of bonds and surface diffusion are responsible for the isotopic fractionation.