Mineral chemistry of MUSES‐C Regio inferred from analysis of dust particles collected from the first‐ and second‐touchdown sites on asteroid Itokawa

The mineralogy and mineral chemistry of Itokawa dust particles captured during the first and second touchdowns on the MUSES‐C Regio were characterized by synchrotron‐radiation X‐ray diffraction and field‐emission electron microprobe analysis. Olivine and low‐ and high‐Ca pyroxene, plagioclase, and merrillite compositions of the first‐touchdown particles are similar to those of the second‐touchdown particles. The two touchdown sites are separated by approximately 100 meters and therefore the similarity suggests that MUSES‐C Regio is covered with dust particles of uniform mineral chemistry of LL chondrites. Quantitative compositional properties of 48 dust particles, including both first‐ and second‐touchdown samples, indicate that dust particles of MUSES‐C Regio have experienced prolonged thermal metamorphism, but they are not fully equilibrated in terms of chemical composition. This suggests that MUSES‐C particles were heated in a single asteroid at different temperatures. During slow cooling from a peak temperature of approximately 800 °C, chemical compositions of plagioclase and K‐feldspar seem to have been modified: Ab and Or contents changed during cooling, but An did not. This compositional modification is reproduced by a numerical simulation that modeled the cooling process of a 50 km sized Itokawa parent asteroid. After cooling, some particles have been heavily impacted and heated, which resulted in heterogeneous distributions of Na and K within plagioclase crystals. Impact‐induced chemical modification of plagioclase was verified by a comparison to a shock vein in the Kilabo LL6 ordinary chondrite where Na‐K distributions of plagioclase have been disturbed.     

D/H ratios of the coexisting phlogopite and richterite from mica nodules and a peridotite in South African kimberlites

The water content and D/H ratio of pairs of phlogopite and richterite in kimberlite samples were measured. The water contents of both minerals were lower than the formula content. On the basis of D/H ratios of the pair, phlogopite and richterite can not be regarded as a simple equilibrium product with respect to hydrogen isotope exchange. It seems impossible to estimate D/H ratio of the mantle water through D/H ratios of the hydrous silicate pairs.     

中部冲绳海沟及伊豆,小笠原伴随海底热水活动的碳素起源

本文对日本中部冲绳海沟，小笠原弧的水了海山、爱丽斯泉与太平洋中央海岭威玛斯海盆等不同大地构造单元中的热水系，运用Ｃ，Ｎｅ，Ｎ等元素－同位素地球化学方法进行分析，对比和研究，并探讨了热水系中碳氮的来源，为大地构造单元的划分对比，提供了新的地球化学依据。     

Evolution of the tertiary volcanic rocks in the Izu-Mariana arc

Petrological evolution of the Tertiary island arc in the Izu-Mariana region has been accompanied by the development of three different volcanic suites: 1) oceanridge basalt now exposed as the metamorphic basement on Yap; 2) island-arc tholeiites of Eocene to early Oligocene age characterized by low contents of incompatible elements at all levels of silica enrichment; and 3) calc-alkalic rocks of late Oligocene to early Miocene age showing higher contents of silica and incompatible elements. All these three suites have primitive, undifferentiated basalts or andesites (boninites) characterized by high Mg/Fe, Cr, and Ni, suggesting that they have been derived from an upper mantle peridotite at relatively high temperatures. The earliest volcanism appears to have occurred at a spreading ridge. Later, as subduction proceeded, the island-arc tholeiite magma may have been produced by the introduction of a smaller amount of water into the locus of fusion from the subducted oceanic crust. An increasingly larger amount of water introduced into the same region could have led to the development of the more siliceous, calc-alkalic magma, as represented typically by the boninite.     

Mineralogy and hydrogen isotope geochemistry of clay minerals in the Ohnuma geothermal area,Northeastern Japan

Mineralogical and hydrogen isotopic studies have been made on clay minerals occurring in the Ohnuma geothermal area, northeastern Japan. Here, clay minerals such as smectite, kaolinite, dickite, sericite, and chlorite were formed by hydrothermal alteration of Miocene rocks. A chemical equilibrium can be assumed to be attained from the fact that the amount of expandable layer in the interstratified chlorite/smectite decreases and the polytype of sericite changes from 1M to 2M₁ with increasing depth and temperature. The hydrogen isotopic composition (D/H) of the clay minerals is lighter than that of the geothermal and local meteoric waters by about 20–40‰. The hydrogen isotopic fractionation factors α_{mineral-water} are as follows: 0.972–0.985 for kaolinite and dickite, 0.973–0.977 for sericite, and 0.954–0.987 for chlorite. In the temperature range from 100 to 250°C, the hydrogen isotopic fractionation factors between these minerals and water are not sensitive to the temperature. α_{chlorite-water} depends on the kind of octahedrally coordinated cations which lie close to the hydroxyl groups; it becomes large with an increase of Mg content of chlorite.