The Tiger Sulfide Chimney,Yonaguni Knoll IV Hydrothermal Field,Southern Okinawa Trough,Japan: The First Reported Occurrence of Pt–Cu–Fe‐Bearing Bismuthinite and Sn‐Bearing Chalcopyrite in an Active Seafloor Hydrothermal System

A sulfide chimney ore sampled from the flank of the active Tiger vent area in the Yonaguni Knoll IV hydrothermal field, south Okinawa trough, consists of anhydrite, pyrite, sphalerite, galena, chalcopyrite and bismuthinite. Electron microprobe analysis indicates that the chalcopyrite contains up to 2.4 wt% Sn, whereas bismuthinite contains up to 1.7 wt% Pt, 0.8 wt% Cu and 0.5 wt% Fe. The Sn‐rich chalcopyrite and Pt–Cu–Fe‐bearing bismuthinite are the first reported occurrence of such minerals in an active submarine hydrothermal system. The results confirm that Sn enters the chalcopyrite as a solid solution towards stannite by the coupled substitution of Sn⁴⁺Fe²⁺ for Fe³⁺Fe³⁺, whereas Pt, Cu and Fe enter the bismuthinite structure as a solid solution during rapid nucleation. The fluid inclusions homogenization temperatures in anhydrite (220–310°C) and measured end‐member temperature of the vent fluids on‐site (325°C) indicate that Sn‐bearing chalcopyrite and Pt–Cu–Fe‐bearing bismuthinite express the original composition of the minerals that precipitated as metastable phases at a temperature above 300°C. The result observed in this study implies that sulfides in ancient volcanogenic massive sulfide deposits have similar trace element distribution during nucleation but it is remobilised during diagenesis, metamorphism or supergene enrichment processes.     

Isotopic composition of gas hydrates in subsurface sediments from offshore Sakhalin Island, Sea of Okhotsk

Hydrate-bearing sediment cores were retrieved from recently discovered seepage sites located offshore Sakhalin Island in the Sea of Okhotsk. We obtained samples of natural gas hydrates and dissolved gas in pore water using a headspace gas method for determining their molecular and isotopic compositions. Molecular composition ratios C₁/_C2+ from all the seepage sites were in the range of 1,500–50,000, while δ¹³C and δD values of methane ranged from ?66.0 to ?63.2‰ VPDB and ?204.6 to ?196.7‰ VSMOW, respectively. These results indicate that the methane was produced by microbial reduction of CO₂. δ¹³C values of ethane and propane (i.e., ?40.8 to ?27.4‰ VPDB and ?41.3 to ?30.6‰ VPDB, respectively) showed that small amounts of thermogenic gas were mixed with microbial methane. We also analyzed the isotopic difference between hydrate-bound and dissolved gases, and discovered that the magnitude by which the δD hydrate gas was smaller than that of dissolved gas was in the range 4.3–16.6‰, while there were no differences in δ¹³C values. Based on isotopic fractionation of guest gas during the formation of gas hydrate, we conclude that the current gas in the pore water is the source of the gas hydrate at the VNIIOkeangeologia and Giselle Flare sites, but not the source of the gas hydrate at the Hieroglyph and KOPRI sites.     

Analysis of RC slab–beam–column sub‐assemblages subjected to bidirectional lateral cyclic loading using a new 3D macroelement

An existing two‐dimensional macroelement for reinforced concrete beam–column joints is extended to a three‐dimensional macroelement. The three‐dimensional macroelement for beam–column joints consists of six rigid interface plates and uniaxial springs for concrete, steel, and bond–slip, which model the inside of a beam–column joint. The mechanical models for the materials and the stiffness equation for the springs are also presented. To validate the model, we used test results from three slab–beam–column sub‐assemblages subjected to bi‐lateral cyclic load. It is revealed that the new joint model is capable of capturing the strength of beam–column joints and the bidirectional interaction in joint shear response, including the concentration of damage in the beam–column joint, the pinching nature in hysteretic behavior, the stiffness degradation, and strength deterioration resulting from cyclic and bidirectional loading. Copyright © 2017 John Wiley & Sons, Ltd.     

Cathodoluminescence microscopy and spectroscopy of forsterite from Kaba meteorite: An application to the study of hydrothermal alteration of parent body

Highly forsteritic olivine (Fo: 99.2–99.7) in the Kaba meteorite emits bright cathodoluminescence (CL). CL spectra of red luminescent forsterite grains have two broad emission bands at approximately 630 nm (impurity center of divalent Mn ions) in the red region and above 700 nm (trivalent Cr ions) in the red–IR region. The cores of the grains show CL blue luminescence giving a characteristic broad band emission at 400 nm, also associated with minor red emissions related to Mn and Cr ions. CL color variation of Kaba forsterite is attributed to structural defects. Electron probe microanalyzer (EPMA) analysis shows concentrations of Ca, Al, and Ti in the center of the forsterite grain. The migration of diffusible ions of Mn, Cr, and Fe to the rim of the Kaba meteoritic forsterite was controlled by the hydrothermal alteration at relatively low temperature (estimated at about 250 °C), while Ca and Al ions might still lie in the core. A very unusual phase of FeO (wüstite) was also observed, which may be a terrestrial alteration product of FeNi‐metal.     

Near-Infrared Photometric And Polarimetric Observations Of Comet Hale-Bopp

Near-infrared photometric and polarimetric observations of comet Hale-Bopp (1995 O1) using KONIC (Kiso Observatory Near-Infrared Camera) are reported. Observations were carried out on March 18 UT and April 26 UT 1997, when the heliocentric distances of the comet were 0.94 and 1.02 AU, and the phase angles were 48.5 deg and 32.9 deg, respectively. In the J, H, and K′ bands, we obtained linear polarization of the near-nucleus region of 16.4 ± 1.2, 18.8 ± 1.3, and 15.1 ± 0.9 percent on March 18UT and 7.1 ± 1.1, 8.9 ± 1.0, and 6.9 ± 0.6 percent on April 26, respectively. These values were higher than those observed for 1P/Halley. The maximum polarization was found at H band on both dates. Polarization maps showed higher polarization regions toward the anti-solar direction in the J and H bands. No distinct correlation was found between high polarization regions and bright regions. The projected expansion velocity of the arc structure of the dust jet was 375 ± 35.7 m/s on 17–19 March. The periodicity was found to be 11.1 ± 2.8 hours. This revised version was published online in July 2006 with corrections to the Cover Date.     

Research on the seismotectonics of the January 17, 1995 Hanshin M 7.2 earthquake

Based on the geological tectonics, aftershock activity, earthquake surface rupture and peak ground motion, the geometric and dynamic characteristics of seismogenic tectonics about the 1995 Hanshin earthquake are analysed. Nojima fault and Rokko fault have the same trending direction, but opposite dips. Their rising and falling plates are in symmetrically diagonal distribution. The two faults can be defined as thrust-strike slip faults and constitute a pivotal strike-slip fault. The earthquake just occurred at the pivot, which is the seismotectonics for the earthquake to develop and occur. The pivotal movement along a strike-slip fault often leads to the occurrence of large earthquakes, whose dynamic process can be demonstrated by the stress analysis on the torsion of a beam with rectangle section. The displacement of earthquake surface rupture, aftershock density and peak acceleration change in a certain range of epicentral distance just similar as the shear stress changes from the center to the sides in the rectangle section. The distribution characteristics of the heaviest damage areas are also discussed in the article from the aspects of special geological tectonics and seismotectonic condition. The result obtained from the article can be applied not only to realizing the potencial earthquake sources in middle-long time, but also to build reasonably the prediction model about earthquake hazard.     

Detection and Evaluation of Gas Hydrates in the Eastern Nankai Trough by Geochemical and Geophysical Methods

Abstract: Interstitial waters extracted from the sediment cores from the exploration wells, “BH‐1” and “MITI Nankai Trough”, drilled ～60 km off Omaezaki Peninsula in the eastern Nankai Trough, were analyzed for the chloride and sulfate concentrations to examine the depth profiles and occurrence of subsurface gas hydrates. Cored intervals from the seafloor to 310 mbsf were divided into Unit 1 (～70 mbsf, predominated by mud), Unit 2 (70–150 mbsf, mud with thin ash beds), Unit 3 (150–250+ mbsf, mud with thin ash and sand), and Unit 4 (275–310 mbsf, predominated by mud). The baseline level for Cl “concentrations was 540 mM, whereas low chloride anomalies (103 to 223 mM) were identified at around 207 mbsf (zone A), 234–240 mbsf (zone B), and 258–265 mbsf (zone C) in Unit 3. Gas hydrate saturation (Sh %) of sediment pores was calculated to be 60 % (zone A) to 80 % (zones B and C) in sands whereas only a few percent in clay and silt. The total amount of gas hydrates in hydrate‐bearing sands was estimated to be 8 to 10 m³ of solid gas hydrate per m², or 1.48 km³ CH₄ per 1 km². High saturation zones (A, B and C) were consistent with anomaly zones recognized in sonic and resistivity logs. 2D and high‐resolution seismic studies revealed two BSRs in the study area. Strong BSRs (BSR‐1) at ～263 mbsf were correlated to the boundary between gas hydrate‐bearing sands (zone C) and the shallower low velocity zone, while the lower BSRs (BSR‐2) at～289 mbsf corresponded to the top of the deeper low velocity zone of the sonic log. Tectonic uplift of the study area is thought to have caused the upward migration of BGHS. That is, BSR‐1 corresponds to the new BGHS and BSR‐2 to the old BGHS. Relic gas hydrates and free gas may survive in the interval between BSR‐1 and BSR‐2, and below BSR‐2, respectively. Direct measurements of the formation temperature for the top 170 m interval yield a geothermal gradient of ～4.3d?C/ 100 m. Extrapolation of this gradient down to the base of gas hydrate stability yields a theoretical BGHS at～230 mbsf, surprisingly ～35 m shallower than the base of gas hydrate‐bearing sands (zone C) and BSR‐1. As with the double BSRs, another tectonic uplift may explain the BGHS at unreasonably shallow depths. Alternatively, linear extrapolation of the geothermal gradient down to the hydrate‐bearing zones may not be appropriate if the gradient changes below the depths that were measured. Recognition of double BSRs (263 and 289 mbsf) and probable new BGHS (～230 mbsf) in the exploration wells implies that the BGHS has gradually migrated upward. Tectonically induced processes are thought to have enhanced dense and massive accumulation of gas hydrate deposits through effective methane recycling and condensation. To test the hypothetical models for the accumulation of gas hydrates in Nankai accretionary prism, we strongly propose to measure the equilibrium temperatures for the entire depth range down to the free gas zone below predicted BGHS and to reconstruct the water depths and uplift history of hydrate‐bearing area.     

Accretion process of the moon

Recent geochemical and geophysical data suggest that the initial temperature of the Moon was strongly peaked toward the lunar surface. To explain such an initial temperature distribution, a simple model of accretion process of the Moon is presented. The model assumes that the Moon was formed from the accumulation of the solid particles or gases in the isolated, closed cloud. Two equations are derived to calculate the accretion rate and surface temperature of the accreting Moon. Numerical calculations are made for a wide range of the parameters particle concentration and particle velocity in the cloud. A limited set of the parameters gives the initial temperature profiles as required by geochemical and geophysical data. These models of the proto-moon cloud indicate that the lunar outershell, about 400 km thick, was partially or completely molten just after the accretion of the Moon and that the Moon should have been formed in a period shorter than 1000 yr. If the Moon formed at a position nearer to the Earth than its present one, the Moon might have been formed in a period of less than one year.On leave from Geophysical Institute, University of Tokyo.Contribution No. 2104, Division of Geological and Planetary Sciences, California Institute of Technology.     

Sequentially sampled gas hydrate water,coupled with pore water and bottom water isotopic and ionic signatures at the Kukuy mud volcano,Lake Baikal: ambiguous deep-rooted source of hydrate-forming water

The isotopic and ionic composition of pure gas hydrate (GH) water was examined for GHs recovered in three gravity cores (165–193 cm length) from the Kukuy K-9 mud volcano (MV) in Lake Baikal. A massive GH sample from core St6GC4 (143–165 cm core depth interval) was dissociated progressively over 6 h in a closed glass chamber, and 11 sequentially collected fractions of dissociated GH water analyzed. Their hydrogen and oxygen isotopic compositions, and the concentrations of Cl^– and HCO₃ ^– remained essentially constant over time, except that the fraction collected during the first 50 minutes deviated partly from this pattern. Fraction #1 had a substantially higher Cl^– concentration, similar to that of pore water sampled immediately above (135–142 cm core depth) the main GH-bearing interval in that core. Like the subsequent fractions, however, the HCO₃ ^– concentration was markedly lower than that of pore water. For the GH water fractions #2 to #11, an essentially constant HCO₃ ^–/Cl^– ratio of 305 differed markedly from downcore pore water HCO₃ ^–/Cl^– ratios of 63–99. Evidently, contamination of the extracted GH water by ambient pore water probably adhered to the massive GH sample was satisfactorily restricted to the initial phase of GH dissociation. The hydrogen and oxygen isotopic composition of hydrate-forming water was estimated using the measured isotopic composition of extracted GH water combined with known isotopic fractionation factors between GH and GH-forming water. Estimated δD of ?126 to ?133‰ and δ¹⁸O of ?15.7 to ?16.7‰ differed partly from the corresponding signatures of ambient pore water (δD of ?123‰, δ¹⁸O of ?15.6‰) and of lake bottom water (δD of ?121‰, δ¹⁸O of ?15.8‰) at the St6GC4 coring site, suggesting that the GH was not formed from those waters. Observations of breccias in that core point to a possible deep-rooted water source, consistent with published thermal measurements for the neighboring Kukuy K-2 MV. By contrast, the pore waters of core St6GC4 and also of the neighboring cores GC2 and GC3 from the Kukuy K-9 MV show neither isotopic nor ionic evidence of such a source (e.g., elevated sulfate concentration). These findings constrain GH formation to earlier times, but a deep-rooted source of hydrate-forming water remains ambiguous. A possible long-term dampening of key deep-water source signatures deserves further attention, notably in terms of diffusion and/or advection, as well as anaerobic oxidation of methane.