Primary melt from Sannome-gata volcano,NE Japan arc: constraints on generation conditions of rear-arc magmas

The conditions under which rear-arc magmas are generated were estimated using primary basalts from the Sannome-gata volcano, located in the rear of the NE Japan arc. Scoriae from the volcano occur with abundant crustal and mantle xenoliths, suggesting that the magma ascended rapidly from the upper mantle. The scoriae show significant variations in their whole-rock compositions (7.9–11.1 wt% MgO). High-MgO scoriae (MgO > ~9.5 wt%) have mostly homogeneous ⁸⁷Sr/⁸⁶Sr ratios (0.70318–0.70320), whereas low-MgO scoriae (MgO < ~9 wt%) have higher ⁸⁷Sr/⁸⁶Sr ratios (>0.70327); ratios tend to increase with decreasing MgO content. The high-MgO scoriae are aphyric, containing ~5 vol% olivine microphenocrysts with Mg# [100 × Mg/(Mg + Fe²⁺)] of up to 90. In contrast, the low-MgO scoriae have crustal xenocrysts of plagioclase, alkali feldspar, and quartz, and the mineralogic modes correlate negatively with whole-rock MgO content. On the basis of these observations, it is inferred that the high-MgO scoriae represent primary or near-primary melts, while the low-MgO scoriae underwent considerable interaction with the crust. Using thermodynamic analysis of the observed petrological features of the high-MgO scoriae, the eruption temperature of the magmas was constrained to 1,160–1,220 °C. Given that the source mantle was depleted MORB-source mantle, the primary magma was plausibly generated by ~7 % melting of a garnet-bearing spinel peridotite; taking this into consideration, and considering the constraints of multi-component thermodynamics, we estimated that the primary Sannome-gata magma was generated in the source mantle with 0.5–0.6 wt% H₂O at 1,220–1,230 °C and at ~1.8 GPa, and that the H₂O content of the primary magma was 6–7 wt%. The rear-arc Sannome-gata magma was generated by a lower degree of melting of the mantle at greater depths and lower temperatures than the frontal-arc magma from the Iwate volcano, which was also estimated to be generated by ~15 % melting of the source mantle with 0.6–0.7 wt% H₂O at ~1,250 °C and at ~1.3 GPa.     

Interactive behavior of soil–pile-superstructure system in transient state to liquefaction by means of large shake table tests

Shaking table tests were conducted by means of a large-scale laminar box with 4 m in length, 2 m in width and 2 m in height in order to investigate behavior of a soil-pile-superstructure system in liquefiable ground. A model two-storey structure, supported by a pile group, was set in a saturated sand deposit, and subjected to a sinusoidal base motion with increasing amplitude. Discussions are focused on the transient behavior until soil liquefaction occurs. Main interests are characteristics of springs used in a sway-rocking model and a multi-freedom lumped mass (MFLM) model that are frequently used in soil–pile interaction analysis. The spring constant in the sway-rocking model is represented by restoring force characteristics at the pile head, and that in the MFLM system is represented by an interaction spring connecting the pile to the free field. The transient state prior to soil liquefaction is shown to be important in the design of a pile because dynamic earth pressure shows peak response in this state. The reduction of the stiffness due to excess porewater generation and strain dependent nonlinear behavior is evaluated.     

Multiple sulfur isotope chemostratigraphy across the Permian–Triassic boundary at Chaotian,China: Implications for a shoaling model of toxic deep-waters

Previous studies on multiple sulfur isotopes (³²S, ³³S, and ³⁴S) in sedimentary pyrite at the end-Permian suggested a shoaling of anoxic/sulfidic deep-water contributing to the extinction. This scenario is based on an assumption that the sedimentary sulfur cycle was largely controlled by benthos activity, though a stratigraphic correlation between the sulfur records and ichnofabrics of the sediments at the end-Permian has not yet been examined. We report the multiple sulfur isotopic composition of pyrite in the Permian–Triassic boundary interval at Chaotian, South China. Our data can be generally explained by a mixing of sulfur in sulfide from two different sources: one produced via sulfate reduction in an open system with respect to sulfate and the other produced in a closed system. In particular, the former with the substantially low δ³⁴S (<−40 ‰) and high ∆³³S (up to +0.100 ‰) values was likely produced via water-mass sulfate reduction or via sulfate reduction in oxic sediments with common burrows. The frequent occurrence of small pyrite framboids (mostly <5 μm in diameter) in the Lopingian (Late Permian) Dalong Formation of deep-water facies supports the enhanced water-mass sulfate reduction in an anoxic deep-water mass. The negative ∆³³S values are observed only in the oxic limestones, and no substantial ∆³³S change is observed across the extinction horizon despite of the disappearance of bioturbation. Our results are apparently inconsistent with the previous shoaling model. We expand the model and infer that, when the deep-water was sulfidic and its shoaling rate was high, a substantial amount of hydrogen sulfide (H₂S) was supplied onto the shelf via the shoaling; that resulted in the positive ∆³³S value of the bulk sediments. The observed ∆³³S variation on a global scale suggests a substantial variation in H₂S concentration and/or in upwelling rate of shoaling deep-waters during the Permian–Triassic transition.     

Internal differentiation of Kutsugata lava flow from Rishiri Volcano,Japan: Processes and timescales of segregation structures' formation

Internal differentiation processes in a solidifying lava flow were investigated for the Kutsugata lava flow from Rishiri Volcano in northern Japan. In a representative 6-m thick lava flow that was investigated in detail in this study, segregation products darker than the host lavas manifested mainly in the form of pipes (vesicle cylinders) and layers (vesicle sheets), occurring around 0.5–2.3 m and 2.0–4.0 m above the base, respectively. Both the cylinders and sheets are significantly richer in incompatible elements such as TiO₂ and K₂O than the host lavas, which suggest that these products essentially represent residual melt produced during solidification of the lava flow. Field observation and the geochemical features of the lavas suggest that the vesicle cylinders grew upward from near the base of the flow by continuous feeding of residual melt from the neighboring host lavas to the heads of the cylinders. On the other hand, the vesicle sheets were produced in situ in the solidifying lava flow as fracture veins caused by horizontal compression. The vesicle cylinders have a remarkably higher MgO content (up to 8 wt.%) than the host lava (< 6 wt.%), whereas the vesicle sheets display MgO depletion (as low as 3.5 wt.%). The relatively high MgO content of the vesicle cylinders cannot be explained solely by the mechanical mixing of olivine phenocrysts with the residual melt. It is suggested that the vesicle cylinders were produced by the extraction of olivine-bearing interstitial melt from an augite-plagioclase network in the host lava, whereas the vesicle sheets were formed by the migration of the residual melt from a crystal network consisting of plagioclase, augite, and olivine in the host lava into platy fractures. We infer that this selective crystal fractionation for forming the vesicle cylinders resulted from processes in which abundant vesicles rejected from the upward-migrating floor solidification front prevented olivine crystals from being incorporated into the crystal network in the host lava. The vesicle cylinders are considered to have formed in ∼ 1 day after the lava flow came to rest, while relatively large vesicle sheets (> 1 cm thick) appeared much later (after ∼ 9 days). The formation of these segregation products was essentially complete within 20 days after the lava emplacement.     

Bioaccumulation of nitroarenes in bivalves at Osaka Bay, Japan

This paper reports for the first time the detection and occurrence of nitroarenes (NPAHs) in marine organisms. Mussels and oysters collected from Osaka Bay, Japan, had total NPAHs concentrations that ranged from 2380 to 24,688 pg/g dry and 2672 to 25,961 pg/g dry, respectively. Relatively higher concentrations were detected in sampling sites located near the central district and suburbs of Osaka City implying that the most probable sources of NPAHs in the two bivalves are exhaust gases and smokes emitted by automobiles and industrial plants. Bivalves had relatively higher residues of 1-nitronaphthalene, 2-nitronaphthalene, 3-nitrophenanthrene, and 9-nitrophenanthrenes. Residues of 2-nitrofluorene, 1-nitropyrene, 4-nitropyrenes, and 6-nitrochrysene were much lower compared to nitronaphthalenes and nitrophenanthrenes. Inter-species differences was only observed for 2-nitronaphthalene with oysters exhibiting significantly higher residues than mussels.     

Microbial responses using denaturing gradient gel electrophoresis to oil and chemical dispersant in enclosed ecosystems

Microbial responses to the addition of oil with or without a chemical dispersant were examined in mesocosm and microcosm experiments by using denaturing gradient gel electrophoresis of bacterial ribosomal DNA and direct cell counting. When a water-soluble fraction of oil was added to seawater, increases in cell density were observed in the first 24h, followed by a decrease in abundance and a change in bacterial species composition. After addition of an oil-dispersant mixture, increases in cell density and changes in community structure coincided, and the amount of bacteria remained high. These phenomena also occurred in response to addition of only dispersant. Our results suggest that the chemical dispersant may be used as a nutrient source by some bacterial groups and may directly or indirectly prevent the growth of other bacterial groups.     

Simulated distribution and ecotoxicity-based assessment of chemically-dispersed oil in Tokyo Bay

To assess risks of chemically-dispersed oil to marine organisms, oil concentrations in the water were simulated using a hypothetical spill accident in Tokyo Bay. Simulated oil concentrations were then compared with the short-term no-observed effect concentration (NOEC), 0.01 mg/L, obtained through toxicity tests using marine diatoms, amphipod and fish. Area of oil concentrations higher than the NOEC were compared with respect to use and non-use of dispersant. Results of the simulation show relatively faster dispersion near the mouth of the bay compared to its inner sections which is basically related to its stronger water currents. Interestingly, in the inner bay, a large area of chemically-dispersed oil has concentrations higher than the NOEC. It seems emulsifying oil by dispersant increases oil concentrations, which could lead to higher toxicity to aquatic organisms. When stronger winds occur, however, the difference in toxic areas between use and non-use of dispersant is quite small.     

Simulations of deep pencil-beam redshift surveys

We create mock pencil-beam redshift surveys from very large cosmological N -body simulations of two cold dark matter (CDM) cosmogonies, an Einstein–de Sitter model ( τ CDM) and a flat model with Ω₀=0.3 and a cosmological constant (ΛCDM). We use these to assess the significance of the apparent periodicity discovered by Broadhurst et al. Simulation particles are tagged as 'galaxies' so as to reproduce observed present-day correlations. They are then identified along the past light-cones of hypothetical observers to create mock catalogues with the geometry and the distance distribution of the Broadhurst et al. data. We produce 1936 (2625) quasi-independent catalogues from our τ CDM (ΛCDM) simulation. A couple of large clumps in a catalogue can produce a high peak at low wavenumbers in the corresponding one-dimensional power spectrum, without any apparent large-scale periodicity in the original redshift histogram. Although the simulated redshift histograms frequently display regularly spaced clumps, the spacing of these clumps varies between catalogues and there is no 'preferred' period over our many realizations. We find only a 0.72 (0.49) per cent chance that the highest peak in the power spectrum of a τ CDM (ΛCDM) catalogue has a peak-to-noise ratio higher than that in the Broadhurst et al. data. None of the simulated catalogues with such high peaks shows coherently spaced clumps with a significance as high as that of the real data. We conclude that in CDM universes, the regularity on a scale of ∼130  h ⁻¹ Mpc observed by Broadhurst et al. has a priori probability well below 10⁻³.     

Geochemistry of Gneiss-Granulite transformation in the “incipient charnockite” zones of southern India

Summary Upper amphibolite facies gneisses in the southern Indian Shield show local transformation into veins, clots and patches of orthopyroxene-bearing dry granulites (incipient charnockites). Depending upon the protolith composition, these desiccated zones are classified into ortho- and para-charnockites and have developed within rocks of distinct mineralogy and chemistry at different time intervals through the structurally-controlled influx of carbon dioxide-rich fluids. Our geochemical investigations at five critical quarry sections indicate that the incipient charnockites have undepleted chemistry and very low K/Rb values. In the paracharnockite localities, where granulite formation is characterized by consumption of garnet, biotite and quartz to produce orthopyroxene, loss of Rb and Ba and enrichment of Ti are observed. In contrast, the orthocharnockite localities show marked LILE enrichment with gain of K, Rb and Ba and loss of CaO, suggesting extensive replacement of plagioclase in the gneisses by K-feldspar in the charnockite through K-Na-Ca exchange reactions with influxing carbonic fluids. The marked depletion in Fe, Mg, Ti and P in these rocks correlates with progressive dissolution of hornblende, biotite, magnetite and accessory apatite. Our study indicates that gneiss to granulite transformation, even if on a local scale, is not an isochemical phenomenon, but attended by distinct element mobilities, although they are contrastingly different from the geochemical trends in some regional high grade terrains.

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Geochemie von Gneiss-Granulit-Übergängen in den Incipient Charnockite Zonen von Süd-Indien

Zusammenfassung Gneise der oberen Amphibolit-Fazies im Südteil des Indischen Schildes zeigen lokal Umwandlungen in Adern, and unregelmäßigen Bereichen von orthopyroxen-führenden trockenen Granuliten (Incipient Charnockites). In Abhängigkeit von der Zusammensetzung des Ausgangsgesteins werden diese Zonen in Ortho- und Paracharnockite eingeteilt. Sie entwickelten sich in Gesteinen von charakteristischer mineralogischer und chemischer Zusammensetzung zu verschiedenen Zeit-Intervallen durch die tektonisch kontrollierte Zufuhr von kohlendioxid-reichen Fluiden. Unsere geochemischen Untersuchungen an fünf strategisch ausgewählten Steinbruchen zeigen, daß die Incipient Charnockite eine nicht verarmte chemische Zusammensetzung und sehr niedrige K/Rb Werte haben. In den Paracharnockit-Lokalitäten, wo Granulitbildung charakterisiert wird durch das Verschwinden von Granat, Biotit und Quartz, aus denen Orthopyroxene gebildet werden, ist Verlust von Rb und Ba und Anreicherung an Ti zu beobachten. Im Gegensatz dazu zeigen die Orthocharnockite eindeutige LILE Anreicherung mit Zunahme von K, Rb, und Ba und Verlust von Ca0. Dies weist auf extensiven Ersatz von Plagioklas in den Gneisen durch K-Feldspat in den Charnockiten durch K-Na-Ca Austausch-Reaktionen mit zugeführten C0₂-Fluiden hin. Die deutliche Verarmung an Fe, Mg, Ti und P in diesen Gesteinen wird mit zunehmender Auflösung von Hornblende, Biotit, Magnetit und akzessorischem Apatit erKlärt. Unsere Untersuchungen zeigen, daß die Gneis-Granulit Transformation auch im lokalen Maßstab nicht ein isochemisches Phänomen ist, sondern durch charakteristische Elementtransporte charakterisiert wird. Diese unterscheiden sich jedoch deutlich von den geochemischen Trends, die in einigen regional-metamorphen high grade terrains zu beobachten sind.[/p]