Submarine hydrothermal mineralization in the Okinawa Trough, SW of Japan: an overview

The Okinawa Trough is a heavily sedimented, rifted back-arc basin formed in an intracontinental rift zone. Submarine hydrothermal activity is located within the six back-arc rifts located in the middle and southern Okinawa Trough and its distribution is controlled principally by tectonic factors. Subduction of the Daito and Gagua Ridges beneath the Ryukyu Arc has resulted in fracturing of the brittle lithosphere beneath the Okinawa Trough. Hydrothermal activity is strongest in the volcanic arc-rift migration phenomenon (VAMP) area plus the JADE site and Southernmost Part of the Okinawa Trough (SPOT) area which form the prolongation of these two ridges. These areas are characterized by extremely high heat flow locally. Submarine hydrothermal fluids from the Okinawa Trough tend to be strongly influenced by interaction of the hydrothermal fluids with organic matter in the sediment resulting in high alkalinity and NH₄⁺ concentrations of the fluids. The fluids also contain high concentrations of CO₂ of magmatic origin. Submarine hydrothermal mineralization in the trough is diverse. The CLAM site consists principally of carbonate chimneys. Interaction of the hydrothermal fluid with organic matter in the sediment is particularly strong at this site. This is most probably a sediment-hosted deposit in which sulphide minerals have deposited within the sediment column leaving ‘spent ore-fluids’ to emerge at the seafloor. The JADE site consists of active and inactive sulphide–sulphate chimneys and mounds. The Zn–Pb-rich sulphides at this site contain the highest concentrations of Pb, Ag and Au so far recorded in submarine hydrothermal sulphide deposits. At Minami-Ensei Knoll and Hatoma Knoll, active and inactive chimneys consist principally of anhydrite and barite as a result of phase separation of the hydrothermal fluids beneath the seafloor. An intense black smoker has recently been discovered at Yonaguni Knoll in the SPOT area. If it is confirmed that sulphide mineralization is dominant at this site, this could be a highly prospective area. The most prospective areas for economic-grade minerals in the Okinawa Trough appear to be the JADE site and the SPOT area.     

Study of the star-forming region L379 IRS3 in CH<Subscript>3</Subscript>OH and CS

A molecular cloud and high-velocity outflow associated with the star-forming region L379 IRS3 have been mapped in the 6_?1-5₀E methanol and CS (3-2) lines using the 12-meter Kitt Peak telescope. The estimated CS column density and abundance in the molecular cloud are 8×10¹⁴ cm^?2 and 4×10^?9, respectively. LVG modeling of the methanol emission constrains the gas density in the cloud to (1–4)×10⁵ cm^?3 and the gas kinetic temperature to 20–45 K. The upper limit on the density of the high-velocity gas is 10⁵ cm^?3.     

Hidden melting signatures recorded in the Troodos ophiolite plutonic suite: evidence for widespread generation of depleted melts and intra-crustal melt aggregation

The main plutonic complex of the Troodos ophiolite, north of the Arakapas Fault Zone, has been re-examined both from field and geochemical perspectives. Ion microprobe analyses of clinopyroxene crystal cores show that the range of melt compositions added to the lower crust far exceeds that of published lavas in the main Troodos massif. This suggests that the lower crust acted as a filter into which a large range of melt compositions were added and out of which a homogenised (and generally fractionated) derivative was extracted. This crustal-level aggregation homogenised diverse melt fractions from a broad range of degrees of melting. Depleted melts with U-shaped rare earth element (REE) patterns were a significant component of the melts added to the crust, but because of their low incompatible element abundances, mixing with less depleted melts prior to eruption masked their signature in the lavas. The discovery that highly depleted melts constituted a significant component of the melts added to the Troodos crust, but not of the lavas, demonstrates that the spatial distribution of lava-types is not necessarily a good indicator of where different parental melt compositions are generated within the mantle. Compared with normal mid-ocean ridge basalts, the Troodos parental melts were (1) generally depleted in immobile incompatible trace elements, (2) less depleted in light REE (LREE) than would be expected for the concomitant depletion in middle and heavy REE, (3) enriched in Sr with respect to the LREE and (4) more oxidised. Modelling of these characteristics suggests a mantle source that had previously lost a significant melt fraction under relatively reducing conditions. This was followed by remelting under more oxidising conditions in an environment in which Sr and LREE were added to the source consistent with previous models of a supra-subduction zone setting.     

Risk analysis of landslides – A case study

The effects of uncertainty due to the variability of soil parameters on the risk of landsliding in the Himalayan region are investigated using a random field model combined with slope stability analyses. Effects of spatial variability both in horizontal and vertical directions, number of test samples, variations in piezometric level and the influence of earthquake on the reliability of a typical slope in a slide area are investigated. The results show that the reliability of slopes in the slide area is significantly affected by the coefficients of variation of soil parameters, spatial variations of soil parameters, number of test samples and piezometric variations. The results also show that the assumption of isotropic variations to assess slope reliability isconservative. The results of the study are useful in providing guidelines and pointing to remedial measures in the form of sub-surface drainage to improve slope reliability in the area.     

Fault plane solutions of the january 26th, 2001 bhuj earthquake sequence

A 12-station temporary microearthquake network was established by the Geological Survey of India for aftershock monitoring of the January 26th, 2001 Bhuj earthquake (M _w 7.6) in the Kutch district of Gujarat state, western India. The epicentres of the aftershocks show two major trends: one in the NE direction and the other in the NW direction. Fault-plane solutions of the best-located and selected cluster of events that occurred along the NE trend, at a depth of 15–38 km, show reverse faulting with a large left-lateral strike-slip motion, which are comparable with the main-shock solution. The NW trending upper crustal aftershocks at depth <10 km, on the other hand, show reverse faulting with right-lateral strike-slip motion, and the mid crustal and lower crustal aftershocks, at a depth of 15–38 km, show pure reverse faulting as well as reverse faulting with right-lateral and left-lateral strike-slip motions; these solutions are not comparable with the main-shock solution. It is inferred that the intersection of two faults has been the source area for stress concentration to generate the main shock and the aftershocks.     

Dissolution kinetics of calcite at 50-70 °C: An atomic force microscopic study under near-equilibrium conditions

Direct measurements of calcite faces were performed using in situ atomic force microscopy (AFM) to reveal the dissolution processes as a function of solution saturation state and temperature. Time-sequential AFM images demonstrated that step velocities at constant temperature increased with increasing undersaturation. The anisotropy of obtuse and acute step velocities appeared to become more significant as solutions approached equilibrium and temperature increased. At saturation state Ω > 0.02, a curvilinear boundary was formed at the intersection of two acute steps and the initially rhombohedral etch pit exhibited a nearly triangular shape. This suggests that the and steps may not belong to the calcite-aqueous solution equilibrium system. Further increase in the saturation state (Ω ? 0.3) led to a lack of etch pit formation and dissolution primarily occurred at existing steps, in accordance with Teng (2004). Analysis of step kinetics at different temperatures yielded activation energies of 25 ± 6 kJ/mol and 14 ± 13 kJ/mol for obtuse and acute steps, respectively. The inconsistencies in etch pit morphology, step anisotropy, and step activation energies from the present study with those of studies far-from-equilibrium can be explained by increased influence of the backward reaction, or growth, near-equilibrium. We propose that the backward reaction occurs preferentially at the acute-acute kink sites. The kinetics and effective activation energies of near-equilibrium calcite dissolution presented in this work provide accurate experimental data under likely CO₂ sequestration conditions, and thus are crucial to the development of robust geochemical models that predict the long-term performance of mineral-trapped CO₂.     

Thallium isotope variations in an ore-bearing continental igneous setting: Collahuasi Formation, northern Chile

Thallium is a highly incompatible element and a large fraction of the bulk silicate Earth Tl budget is, therefore, expected to reside in the continental crust. Nonetheless, the Tl isotope systematics of continental rocks are essentially unexplored at present. Here, we present new Tl isotope composition and concentration data for a suite of 36 intrusive and extrusive igneous rocks from the vicinity of porphyry Cu deposits in the Collahuasi Formation of the Central Andes in northern Chile. The igneous lithologies of the rocks are variably affected by the hydrothermal alteration that accompanied the formation of the Cu deposits.The samples display Tl concentrations that vary by more than an order of magnitude, from 0.1 to 3.2 μg/g, whilst ε²⁰⁵Tl ranges between −5.1 and +0.1 (ε²⁰⁵Tl is the deviation of the ²⁰⁵Tl/²⁰³Tl isotope ratio of a sample from a standard in parts per 10⁴). These variations are primarily thought to be a consequence of hydrothermal alteration processes, including metasomatic transport of Tl, and formation/breakdown of Tl-bearing minerals, which are associated with small but significant Tl isotope effects. The Tl abundances show excellent correlations with both K and Rb concentrations but no co-variation with Cu. This demonstrates that Tl displays only limited chalcophile affinity in the continental crust of the Collahuasi Formation, but behaves as a lithophile element with a distribution that is primarily governed by partitioning of Tl⁺ into K⁺-bearing phases. Collahuasi samples with propylitic alteration features, which are derived from the marginal parts of the hydrothermal systems, have, on average, slightly lighter Tl isotope compositions than rocks from the more central sericitic and argillic alteration zones. This small but statistically significant difference most likely reflects preferential retention of isotopically heavy Tl in alteration phases, such as white micas and clays, which formed during sericitic and argillic alteration.     

Pathways and regulation of carbon, sulfur and energy transfer in marine sediments overlying methane gas hydrates on the Opouawe Bank (New Zealand)

This study combines sediment geochemical analysis, in situ benthic lander deployments and numerical modeling to quantify the biogeochemical cycles of carbon and sulfur and the associated rates of Gibbs energy production at a novel methane seep. The benthic ecosystem is dominated by a dense population of tube-building ampharetid polychaetes and conspicuous microbial mats were unusually absent. A 1D numerical reaction-transport model, which allows for the explicit growth of sulfide and methane oxidizing microorganisms, was tuned to the geochemical data using a fluid advection velocity of 14 cm yr⁻¹. The fluids provide a deep source of dissolved hydrogen sulfide and methane to the sediment with fluxes equal to 4.1 and 18.2 mmol m⁻² d⁻¹, respectively. Chemosynthetic biomass production in the subsurface sediment is estimated to be 2.8 mmol m⁻² d⁻¹ of C biomass. However, carbon and oxygen budgets indicate that chemosynthetic organisms living directly above or on the surface sediment have the potential to produce 12.3 mmol m⁻² d⁻¹ of C biomass. This autochthonous carbon source meets the ampharetid respiratory carbon demand of 23.2 mmol m⁻² d⁻¹ to within a factor of 2. By contrast, the contribution of photosynthetically-fixed carbon sources to ampharetid nutrition is minor (3.3 mmol m⁻² d⁻¹ of C). The data strongly suggest that mixing of labile autochthonous microbial detritus below the oxic layer sustains high measured rates of sulfate reduction in the uppermost 2 cm of the sulfidic sediment (100-200 nmol cm⁻³ d⁻¹). Similar rates have been reported in the literature for other seeps, from which we conclude that autochthonous organic matter is an important substrate for sulfate reducing bacteria in these sediment layers. A system-scale energy budget based on the chemosynthetic reaction pathways reveals that up to 8.3 kJ m⁻² d⁻¹ or 96 mW m⁻² of catabolic (Gibbs) energy is dissipated at the seep through oxidation reactions. The microorganisms mediating sulfide oxidation and anaerobic oxidation of methane (AOM) produce 95% and 2% of this energy flux, respectively. The low power output by AOM is due to strong bioenergetic constraints imposed on the reaction rate by the composition of the chemical environment. These constraints provide a high potential for dissolved methane efflux from the sediment (12.0 mmol m⁻² d⁻¹) and indicates a much lower efficiency of (dissolved) methane sequestration by AOM at seeps than considered previously. Nonetheless, AOM is able to consume a third of the ascending methane flux (5.9 mmol m⁻² d⁻¹ of CH₄) with a high efficiency of energy expenditure (35 mmol CH₄ kJ⁻¹). It is further proposed that bioenergetic limitation of AOM provides an explanation for the non-zero sulfate concentrations below the AOM zone observed here and in other active and passive margin sediments.     

New observations on Rajahmundry Traps of the Krishna-Godavari Basin

The Rajahmundry Traps of the Krishna Godavari Basin (K-G Basin) consist of three distinct basalt flows interbedded with two intertrappean sedimentary horizons, which in turn are underlain by the late Cretaceous fossiliferous limestone bed (infratrappean) and overlain by the Cenozoic Rajahmundry Formation (conglomerate/sandstone). Among the three, the lower flow is characterized by the presence of the physical volcanological features such as rootless cones, tumuli and dyke like forms along with single to multitier columnar and radial jointing. The middle and upper flows are simple, massive and vesicular and exhibit spheroidal weathering. Physical volcanological features and lithological attributes indicate that the lower flow was formed by an explosive volcanic activity in hydrous environment, followed by sub aerial eruption to form the middle and upper flows. The fossiliferous limestone bed is a representative horizon for the K-T boundary mass extinction caused due to intense volcanism. Intertrappean sediments exhibit weathered soil profiles (palaeosols) with limestone beds denoting a distinct time gap during various phases of lava eruption. Evaluation of the palaeogeographic scenario of the Krishna and Godavari Rivers does not provide any evidence for the existence of Cretaceous palaeovalley which would have provided pathway for lava transportation from the Deccan volcanic province of western India to the K-G Basin situated along the east coast. The present study opens up an alternative approach to explain the origin of basalt flows at Rajahmundry. In all probability the lavas could be intrabasinal. NW-SE and NESW faults or their intersection zones are probable pathways for lava eruption in the K-G Basin.     

The Darasun gold deposit,Eastern Transbaikal region: Chemical composition,REE patterns,and stable carbon and oxygen isotopes of carbonates from ore veins

The chemistry, REE patterns, and carbon and oxygen isotopic compositions of carbonates from ore veins of the Darasun deposit are discussed. In addition to the earlier described siderite, calcite, and carbonates of the dolomite-ankerite series, kutnahorite is identified. The total REE content in Fe-Mg carbonates of the dolomite-ankerite series (2.8–73 ppm) is much lower than in later calcite (18–390 ppm). δ¹³C of Fe-Mg carbonates and calcite varies from +1.1 to −6.7‰ and from −0.9 to −4.9‰, respectively. δ¹⁸O of Fe-Mg carbonates and calcite varies from +17.6 to 3.6‰ and from +15.7 to −0.5‰, respectively. The REE sum and carbon and oxygen isotopic compositions reveal zonal distribution relative to the central granodiorite porphyry stock. The correlation between the carbon and oxygen isotopic compositions and REE sum reflects variations in the physicochemical formation conditions and composition of ore-forming fluid. The isotopic composition of fluid is calculated, and possible sources of its components are considered. Earlier established evidence for a magmatic source of ore-forming fluid and participation of meteoric water in ore formation is confirmed. Geochemical evidence for interaction of ore-forming fluid with host rocks is furnished. The relationships between the REE sum, on the one hand, and carbon and oxygen isotopic compositions of hydrothermal ore-forming fluid, on the other, are established.