Structure and crystal chemistry of hydrous wadsleyite, Mg1.75SiH0.5O4: possible hydrous magnesium silicate in the mantle transition zone

The crystal structure of hydrous wadsleyite, Mg_1.75SiH_0.5O₄ synthesized in an MA 8-type apparatus at conditions of 1300°C and 15.5 GPa, has been analyzed and refined in space group Imma, using the X-ray intensities measured on a 60X60X10 μm single crystal. The composition (Z=8) and unit cell are Mg_1.74Si_0.97H_0.65O₄ by E.P.M.A. analysis and a=5.663(1) Å, b= 11.546(2) Å, c=8.247(4) Å, V=539.2(5) ų. The partial M-site occupancies were determined; vacancies associated with the incorporation of water are strongly concentrated on the Mg 3 site. The OH in the structure was confirmed by Raman and FTIR spectroscopies. The result of valence sum calculation based on the refined bond lengths indicates that O1 is a hydroxyl. The formula of hydrous wadsleyite can be expressed as Mg_2-xSiH_2xO₄, where 0≤x≤0.25. When x=0.25, all of the O1 site is hydroxyl and the maximum solubility of 3.3 wt% H₂O is realized. Structural relations to other dense hydrous phases are discussed.     

Performance of a lithium fluoride bolometer for Tokyo dark matter search experiment

The performance of a 21-g lithium fluoride bolometer is presented. The background spectrum was measured in the surface laboratory. We derive an exclusion plot for the spin-dependent coupled Weakly Interacting Massive Particles (WIMPs) cross section.     

Partitioning of Ni2+, Co2+, Fe2+, Mn2+ and Mg2+ between olivine and silicate melts: compositional dependence of partition coefficient

Partitioning of Ni²⁺, Co²⁺, Fe²⁺, Mn²⁺ and Mg²⁺ between olivine and silicate melts has been determined near the join (Mg_0.5·-Fe_0.5)₂SiO₄-K₂O 4SiO₂ and for seven different basaltic compositions. The experiments were made at 1 atm total pressure, 1500-1100°C, and under moderate to reducing oxygen fugacities. The concentration factor, defined as K^MO = (MO)^ol/(MO)^liq (molar ratio), increases markedly for all the cations studied as the olivine component of the liquid decreases. Much of the increase in K^MO is considered as due to the compositional effect of the coexisting liquid: the temperature effect on K^MO is probably opposite to the compositional effect (K^MO decreases as temperature decreases).The partition coefficient K^MO-MgO = (MO/MgO)^ol/(MO/MgO)^liq for the reaction, M_ol²⁺ + Mg_liq²⁺ = M_liq²⁺ + Mg_ol²⁺. is relatively constant over a wide range of SiO₂ content of the liquid, except in the case of Ni²⁺. The partition coefficients have similar ranges both in synthetic and natural rock systems: K^NiO-MgO = 1.8–3.0, K^CoO-MgO = 0.6–0.8, K^FeO-MgO = 0.27–0.38, and K^MnO-MgO = 0.23–0.32. There is a systematic variation in the partition coefficient K^MO-MgO with the composition of liquid; K^MO-MgO increases with increasing SiO₂ content of melt. The partition coefficients for Co²⁺, Fe²⁺ and Mn²⁺ are useful to test the equilibration of olivine with magma of a wide compositional range.     

10Be dating of North Pacific sediment cores up to 2.5 million years B.P.

The¹⁰Be method of dating of marine sediment cores is applied to five North Pacific cores. Assuming a constant¹⁰Be precipitation rate and varying sedimentation rates with time during the past 2.5 m.y. dating confirms to that obtained from paleomagnetic stratigraphy. The¹⁰Be concentration variations with depth in the cores are primarily due to changes in sediment dilution and do not reflect cosmic ray intensity or global climate variations. The limits of¹⁰Be deposition rate variation in the investigated cores are less than ± 10% for periods of (2–7) × 10⁵ years and less than ±30% for periods of 1 × 10⁵ years. The data set gives a half-life of¹⁰Be is 1.50 × 10⁶ years. The latitudinal effect of¹⁰Be concentrations and¹⁰Be/⁹Be ratios relates to a frequency of particulate matter occurrence (detrital and biological particles) in the oceans and to oceanic circulation.     

10Be in marine sediments

The depth profile of the long-lived radionuclide¹⁰Be in a marine sediment recovered in the vicinity of the Samoan Islands has been precisely assayed with a highly sensitive needle-type gas counter. The obtained irregular pattern of¹⁰Be concentrations with depths ranging from 4.7 to 0.3 dpm/kg dry sediment is interpreted as being due to dilution of¹⁰Be by volcanic eruptions in the past.     

Current activities in aerobiology in Japan

A brief review of the research activities of Japanese scientists in aerobiology, which is one of the interdisciplinary sciences closely related to atmospheric turbulence and diffusion as well as to biology, is presented in order to make contacts with interested scientists in other countries.     

Application of Chlorite Geothermometry to Hydrothermal Alteration in Toyoha Geothermal System, Southwestern Hokkaido, Japan

In this study, we applied chemical geothermometers to the estimation of formation temperatures of chlorites from various types of hydrothermally altered rocks in the Toyoha geothermal field, using core samples from six drill holes (TH-2 to TH-7) together with wasted ore samples from Toyoha vein-type ore deposit. Based on the preliminary examination of mineral assemblages by X-ray powder diffraction and optical microscopy, hydrothermal alteration observed through the drill holes was classified into four types of alteration zones: propylitic, mixed-layer minerals, kaolin minerals, and ore mineralized zones. The mineral assemblage of the ore mineralized zone observed through TH-2, TH-4, and TH-6 is similar to those of Toyoha ore veins reported previously. The Fe³⁺/ΣFe ratios of chlorites were determined by X-ray photoelectron spectroscopy (XPS), in addition to the usual microprobe analyses. The ratios ranged from 0.20–0.26 for chlorites from the propylitic alteration zone and from 0.13 to 0.17 for those from the ore mineralized zone associated with sulfide minerals. After correcting the Fe³⁺ contents in the octahedral sites of chlorite structures, we obtained acceptable temperatures of the chlorite formation by application of geothermometers, for instance, a similar range of 150–300°C for chlorites from either the propylitic zone or the ore mineralized zone developed through TH-2, TH-4, and TH-6. Chlorites from the ore mineralized zone proximal to the Toyoha deposit are characterized by high Fe and Mn contents compared to the propylitic chlorites, which is similar to the Toyoha vein-filling chlorites; the formation temperatures were close to both the homogenization temperatures of fluid inclusions and the present subsurface temperatures measured through drill holes. Chlorites from the Toyoha ore veins, however, gave slightly higher formation temperatures (180–350°C) than those of chlorites from the ore mineralized zone in the drill cores. This suggests that several types of hydrothermal alteration occurred at different stages in the Toyoha geothermal field and the composition of product chlorite was controlled not only by the temperature but also the composition of fluid related to the formation. Reliable estimation of temperature for the chlorite formation provides basic information on evaluating correctly other physicochemical conditions prevalent at the formation.     

Assessment of the level of activity of advective transport through fractures and faults in marine deposits by comparison between stable isotope compositions of fracture and pore waters

Hydrogeology Journal - Assessment of the level of activity of advective transport through faults and fractures is essential for guiding the geological disposal of radioactive waste. In this study,...