Carbon isotopic thermometry and geobarometry of sillimanite isograd in thermal aureoles: the depth of emplacement of upper crustal granitic bodies

Carbon isotope fractionation between coexisting calcite and graphite (C ) has been studied in metamorphosed limestones from three thermal aureoles around Cretaceous granitic bodies (i.e., Tanohata, Tono, and Senmaya aureoles) in the Kitakami Mountains, Northeast Japan. C in each aureole decreases toward the granitic bodies, and becomes virtually uniform near the sillimanite isograd for metapelites, although calcite has variable isotopic ratios reflecting the original sedimentary compositions. The relationships indicate that isotopic equilibrium has been attained in metamorphosed limestone of sillimanite grade. Estimated C at the sillimanite isograd is similar in the Tanohata and Tono aureoles, but different in the Senmaya aureole with smaller carbon isotopic fractionations. From the temperature dependence of C and the negative dP/dT of andalusite–sillimanite equilibrium, we conclude that the sillimanite isograd in the Senmaya aureole was under higher temperature and lower pressure than in the other two localities. Temperatures at the sillimanite isograd are estimated by using existing calibrations of carbon isotopic exchange between calcite and graphite, whereas pressures are estimated from carbon isotopic temperatures and the andalusite–sillimanite equilibrium (Holdaway and Mukhopadhyay 1993a). Consistency of the P–T estimates is examined in the light of phase equilibria in the pelitic system. The estimated pressures at the sillimanite isograd are at about 2.1–2.7(±0.2) kbar for the Tanohata and Tono aureoles and less than 1 kbar for the Senmaya aureole, respectively. Geobarometry of sillimanite isograd in thermal aureoles indicates a marked difference in the depth of solidification of upper crustal granitoids: the Senmaya pluton has intruded and solidified at a very shallow level of less than 4 km whereas the Tanohata and Tono plutons are more deep-seated (ca. 8–10 km). The method can also be an effective tool in studying low-pressure type metamorphism in which geothermobarometry using garnet is not always applicable.Editorial responsibility: J. Hoefs     

Mesoscale Reproducibility in Regional Ocean Modelling with a Three-Dimensional Stratification Estimate Based on Aviso-Argo Data

ABSTRACT

For dynamically consistent, high-resolution, yet cost-effective regional oceanic downscaling modelling, an empirical three-dimensional (3D) density estimate based on publicly available datasets is utilized for the Regional Oceanic Modeling System (ROMS) with simple data assimilation (i.e., TS nudging, where TS stands for temperature and salinity). We rely on a method built upon the two-layer model to reconstruct a mesoscale 3D temperature and salinity field, referred to as Tokyo University of Marine Science and Technology (TUMSAT)-TS, using near real-time altimeter-derived dynamic height along with Argo float profiling data. The TUMSAT-TS is first validated using in situ hydrographic data, then is implemented in the Japan Coastal Ocean Predictability Experiment (JCOPE2)-ROMS downscaling system for the Kuroshio region off Japan. We explore the usability of TUMSAT-TS by carrying out three comparative simulations with temperature and salinity nudging towards the (i) TUMSAT-TS and (ii) JCOPE2-TS fields, and (iii) without the nudging. Whereas the unassimilated case fails to properly account for the Kuroshio, both datasets individually are found to help reproduce the mesoscale variability of the Kuroshio, as well as its transient paths, volume transport, associated kinetic energy (KE) and eddy KE, and seasonally varying stratification.     

祁连山七一冰川物质平衡的最新观测结果

祁连山七一冰川观测结果表明, 2001/2002年度和 2002/2003 年度冰川物质平衡分别为-810mm和-316 mm水当量, 冰面出现显著的减薄状态. 和过去的观测结果相比较, 20 世纪 70 年代为较大的正平衡, 年平均为360 mm水当量; 80年代年平均为4 mm水当量, 基本接近零平衡状态. 到近两年亏损强烈, 为所有观测资料中负平衡值最大的年份, 零平衡线也达到最高位置. 物质平衡出现较大的负值和零平衡线位置升高的状况, 强烈反映了祁连山冰川对气候变暖过程的响应. 如果气候变暖趋势继续, 冰川物质平衡负值将增大、冰面减薄和雪线的升高, 冰川将继续呈现萎缩状态.     

Role of Iron(III) and Aluminum Hydroxides in Concentration/reduction of Au(III) Complexes

Abstract: The adsorption of gold on iron(III) and aluminum hydroxides from solutions containing Au(III) complexes has been studied as a function of pH and chloride concentration at 30C. Iron(III) hydroxide was more effective in adsorbing gold from solution than aluminum hydroxide. However, both hydroxides controlled the behavior of Au(III) complex with very similar manner. The most effective gold adsorption occurred in aqueous solution with near neutral pH and low Cl concentration. In this solution condition, Au(III) complexes were mainly dissolved as AuCl₂(OH)₂^- and AuCl(OH)₃^-, and the surface charge for both hydroxides was positive. In addition, the adsorbed Au(III) complexes were spontaneously reduced to elemental gold in spite of the absence of a specific reducing agent.
The results of this study suggest that adsorption and spontaneous reduction of gold complexes on the surface of hydrous metal oxides with positive charge play an important role in gold precipitation in subsurface environment.