Experimental evidence for diamond-facies metamorphism in the Dora-Maira massif

The peak metamorphic conditions of subducted continental crust in the Dora-Maira massif (Western Alps) have been revised by combining experimental results in the KCMASH system with petrologic information from whiteschists. Textural observations in whiteschists suggest that the peak metamorphic assemblage garnet+phengite+kyanite+coesite±talc originates from the reaction kyanite+talc↔garnet+coesite+liquid. In the experimentally determined petrogenetic grid, this reaction occurs above 45 kbar at 730 °C. At lower pressures, talc reacts either to orthopyroxene and coesite or, together with phengite, to biotite, coesite and kyanite. The liberated liquid contains probably similar amounts of H₂O and dissolved granitic components. The composition of the liquid in the whiteschists at peak metamorphic conditions, a major unknown in earlier studies, was probably very similar to the liquid composition produced in the experiments. Therefore, the experimentally determined petrogenetic grid represents a good model for the estimation of the peak metamorphic conditions in whiteschists. Experimentally determined Si-isopleths for phengite further constrain peak pressures to 43 kbar for the measured Si=3.60 of phengite in the natural whiteschists. All these data provide evidence that the whiteschists reached diamond-facies conditions.

The fluid-absent equilibrium 4 kyanite+3 CELADONITE=4 coesite+3 muscovite+pyrope has been calibrated on the basis of garnet and phengite compositions in the experiments and serves as a geothermobarometer for ultra-high-pressure (UHP) metapelites. For graphite-bearing metapelites and kyanite–phengite eclogites, forming the country rocks of the whiteschists, peak metamorphic pressures of about 44±3 kbar were calculated from this barometer for temperatures of 750 °C estimated from garnet–phengite thermometry. Therefore, the whole ultra-high-pressure unit of the Dora-Maira massif most likely experienced peak metamorphic conditions in the diamond stability field. While graphite is common in the metapelites, diamond has not been found so far. The absence of metamorphic microdiamonds might be explained by the low temperature of metamorphism, the absence of a free fluid phase in the metapelites and a short residence time in diamond-facies conditions resulting in kinetic problems in the conversion of graphite to diamond.     

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.     

淮安市典型土动力特性的试验研究

通过对淮安市典型的全新世沉积粉土和粘性土进行室内自振柱试验及粉土的动三轴液化试验，把粉土和粘性土的自振柱试验结果与Seed和Idriss建议的砂土及饱和粘土的剪切模量比G／Gmax-γ曲线和阻尼比λ-γ曲线的变化范围进行对比，结果表明：粉土的剪模量比要比饱和粘土的大，而比砂土的剪模量比要小，其阻尼比接近于砂土的阻尼比；粘性土的剪模量比要比一般饱和粘土的大，而与砂土的剪模量比相近，其阻尼比要比砂土的略低；粉土的抗液化强度与液化振次之间的关系可以用指数函数来表示，其振动孔隙水压力的发展规律可以用反正弦三角函数拟合；粘粒含量是影响淮安市全新世沉积粉土抗液化强度的主要影响因素。     

The crustal fluid evolution and the causes of earthquakes(Ⅲ)

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安山岩中黄铜矿矿石分析和制硫酸铜工艺的研究

安山岩中的黄铜矿是庐江中生代陆相火山热液型铜矿床的原生矿，矿石中主要伴生黄铁矿及少量斑铜矿、赤铁矿和褐铁矿。物相分析结果，黄铜矿的粒度很细，只有细磨才能单体解离；它在矿石中分布极不均匀，且与脉石矿物接触疏松，适于粗磨抛尾。物性分析结果，黄铜矿在４００～５３０℃、斑铜矿在４５０～６００℃、黄铁矿在５００～６８０℃氧化分解。实验研究表明，矿石经磨碎磁选，大部分的粗粒级的铁矿物能够回收；粗磨抛尾可获得铜、硫的粗精矿；然后再经硫酸化焙烧、酸浸、过滤、提纯、浓缩结晶可制得工业级硫酸铜。浸渣做炼铁原料，黄钾铁矾做Ｆｅ２Ｏ３颜料，有时还可回收金、银。     

地壳流体与地幔流体间的关系

通过铀、金矿床及地幔岩捕虏体研究，初步得出以下认识：（１）在热液作用中岩浆分异热液是不存在的；（２）碱交代作用是整个地幔交代作用和地壳交代作用的基本运作机制，现已构成有几十条具体规律的理论系统；碱交代岩是地幔流体转变为热液的化石记录；（３）拆离断层构造体系是地幔流体上升到地壳后的活动通道；（４）磷（Ｐ）是地幔流体的特征性示踪成分；（５）大洋缺氧事件、生物种属灭绝、厄尔尼诺等有共同的地幔流体致因；（６）天然气－油－盐－金属成矿是统一的热液成矿作用。软流体是今后区域成矿预测的重要新依据。软流体的顶部发育有次级、再次级的局部上凸部，这是矿带、矿田群的重要成矿控制因素和找矿新标志。     

Dissolved carbon in pore waters from the carbonate barrier reef of Tahiti (French Polynesia) and its basalt basement

This paper deals with dissolved inorganic carbon (DIC) and organic carbon (DOC) in pore waters from a 150 m deep hole drilled through the carbonate barrier reef of Tahiti and its underlying basalt basement. Alkalinity-pH measurements were used to calculate the DIC species concentration, and DOC was analysed according to the high temperature catalytic oxidation technique. Salinity was used as a conservative tracer to help identify water origin and mixing within the hole. Water mixing, calcium carbonate dissolution and mineralization of organic carbon combined to form three distinct groups of pore water. In the deeper basalt layers, pore water with alkalinity of 1.4 meq kg^–1 pH of 7.6 and p(CO₂) of 1.2 mAtm was undersaturated with respect to both aragonite and calcite. In the intermediate carbonate layer, pore water with alkalinity of more than 2.0 meq kg^–1, pH of 7.70 and p(CO₂) of 1.4 mAtm was supersaturated with respect to both aragonite and calcite. The transition zone between those two groups extended between 80 and 100 m depth. The shift from aragonite undersaturation to supersaturation was mainly attributed to the mixing of undersaturated pore waters from the basalt basement with supersaturated pore waters from the overlaying limestone. In the top of the reef, inputs from a brackish water lens further increased p(CO₂) up to 5.6 times the atmospheric P(CO₂).     

Hydrous pyrolysis of a Type III source: fractionation effects during primary migration in natural and artificially matured samples

A core from the Cambay Shale Formation of the Cambay Basin, containing immature Type III organic matter, was pyrolysed at 300°C for different durations of time to different maturation levels. Fractionation effects were studied employing a three-step extraction technique after removal of the expelled pyrolysate. The extractable organic matter (EOM) obtained on extraction of the whole core is assumed to be that present in open pores, while that obtained on finely crushing the sample is assumed to be that present in closed pores. The EOM obtained from 1 cm chips is termed EOM from semi-open pores. The gross composition of the pyrolysates expelled during pyrolysis is not similar to the oils reservoired in the area, and there is no significant fractionation observed between expelled pyrolysates and unexpelled EOM. Our study indicates movement of fluids between closed, semi-open and open pores. In both systems, there is a higher concentration of EOM in open pores than in semi-open and closed pores, and the fraction of EOM in open pores is much greater in the artificial system than in the natural system. Fractionation effects on n-alkane and isoprenoid hydrocarbon-based parameters were also studied. n-Alkenes are present in semi-open and closed pores of the immature core and in the core after it was pyrolysed to 300°C for 6 and 48 h, but are absent in the open pores. n-Alkenes are present in closed pores in the naturally matured core. Presence of n-alkenes in the pyrolysates expelled during the 6 and 48 h experiments, but their absence in the open pores of the core, indicates that expulsion also occurs through temporary microfractures during laboratory pyrolysis, whereas in the natural system expulsion from closed pores seems to be only via semi-open and open pores.     

Characteristics and origin of sediment-hosted disseminated gold deposits: a review

Sediment-hosted disseminated gold (SHDG) deposits comprise a major portion of the gold production and reserves in the US. Although presently known to be common only in western North America, SHDG deposits are a significant source of world gold production. These deposits are characterized by extremely fine-grained disseminated gold, hosted primarily by arsenian pyrite. Other metals show very little enrichment although in addition to As, anomalous concentrations of elements such as Sb, Hg, Tl and Ba are utilized as exploration tools. The host rocks are dominantly silty carbonates, but ore concentrations are also present in siliceous and silicified rocks as well as intrusive rocks. Alteration consists of decarbonatization, silicification (jasperoid formation) and argillization, which are arranged both spatially and temporally in that order. Argillic alteration is zoned from kaolinite-dominated cores to sericite-dominated margins. The deposits commonly exhibit significant structural (faults) and stratigraphic (composition/permeability) controls. Until the last few years, SHDG deposits were considered as near-surface, epithermal type deposits in origin. Because of their fine-grained nature and the lack of macroscopic features such as veins, it has proven quite difficult to extract geochemical data that are clearly related to their genesis. However, fluid inclusion data indicate pressures corresponding to depths of 2–4 km under lithostatic conditions. Temperatures are constrained by fluid inclusions and phase equilibria to near 225°C. Stable isotope data from alteration minerals and fluid inclusions indicate that the ore fluids were dominated by meteoric waters, some of which had clearly exchanged oxygen with wallrocks during their passage through the crust. Although the data vary, most ore fluids probably had δD values near −150‰ and δ¹⁸O values ranging from −10 to +5‰. Sulfur isotope values reported from SHDG deposits span a wide range, from −30 to +20‰ (sulfides) and 0 to >45‰ (sulfates). Ore-related sulfides (pyrite, realgar) fall at the upper end of the range reported for sulfides. The alteration and mineral assemblage indicate the ore fluids were probably near neutral and gold was likely carried as a bisulfide complex. The depositional mechanism(s) probably included mixing, cooling and oxidation. These mechanisms are consistent with the observed alteration features, i.e. quartz precipitation, calcite dissolution and sericite-kaolinite coexistence. It also explains the presence of both siliceous ores containing native Au and sulfide ores containing Au in pyrite. The extreme variations in sulfur isotopes as seen at Post and fluid inclusion data from Carlin may be indicative of some phase separation (‘boiling’), but such relations have not been documented in other deposits and the importance of phase separation to gold deposition appears minimal.     

A Study on Organic Inclusions in Clastic Reservoir Rocks and Their Application to the Assessment of Oil and Gas Accumulations

Terrigenous clastic reservoir rocks are widespread in China,and nearly all the industrial oil and gas accumulations in eastern China occur in the clastic rocks.The study shows that organic inclusions are mostly distributed in the secondary fissures and pores which were ormed in the process of oil-rock interaction,rather than in the cements or secondary enlargements. The organic inclusions are dominantly organic gas-rich or are composed of pure hydrocarbons.Homogenization temperatures range mainly from 120℃ to 130℃，which shows a relatively high maturity of organic matter.Vertical and horizontal temperature changes provide the grounds for the investigation of basin evolution and thermal fluid-kinetics-model.Fluorescence spectral characteristics o the organic inclusions indicate that oils and gases in the area studied probably have experienced two-stage or two-time migration.Micro-fluorescence rescearch is one of the effective approaches to oil/source correlation and oil migration-stage determination.The abundance and occurrence of organic inclusions is one of the indicators of oil and gas abundance and accumulation in rock layers.With the help of other informatio,organic inclusions can provide the basis for the prospective assessment of oil and gas in clastic reservoir rocks.