蛇绿岩中金刚石和异常矿物的全球记录

蛇绿岩型金刚石产在地幔橄榄岩和铬铁矿中,是新建立的金刚石产出类型,不同于产在金伯利岩和超高压变质岩中的金刚石。全球已在21个蛇绿岩中发现了该类金刚石,含金刚石的蛇绿岩主要分布在特提斯造山带、乌拉尔-中亚造山带、日高变质岩带和北美克拉马斯-阿卡特兰造山带。本文梳理了含金刚石蛇绿岩的全球分布和地质背景以及蛇绿岩中超高压-强还原矿物与其它壳幔矿物组合的特征,讨论了已有的含金刚石铬铁矿和地幔橄榄岩的四种成因机制。金刚石和伴生的超高压-强还原矿物组合产在不同时代的造山带蛇绿岩中,不仅仅揭示了金刚石在蛇绿岩中普遍存在,需要重新思考蛇绿岩和铬铁矿的成因以及它们形成的地质构造背景,还证实了蛇绿岩地幔橄榄岩和铬铁矿是地球深部矿物重要的储存库,为认识地球深部的物质组成和物理化学环境,以及深部物质运移的轨迹和动力学过程等提供了天然样品。     

Geochemistry and formation conditions of rare-metal granites with various fluorine-bearing minerals (fluorite,topaz, and cryolite)

A comparative geochemical study of rare-metal granitoids with various fluorine-bearing minerals (fluorite, topaz, and cryolite) was carried out. It was shown that these rocks correspond to both plumasitic and agpaitic geochemical types. The fluorite-, topaz-, and cryolite-bearing granites of these geochemical types are distinctly different in geochemical parameters and the character of magmatic evolution. These differences are related to the composition of initial magmas and their sources. Rare-metal granitoids with fluorine-bearing minerals compose small massifs, stocks, and dike swarms. Their formation is independent of the composition and age of the country rocks or geologic structures where they occur. Original Russian Text ? V.S. Antipin, E.A. Savina, M.A. Mitichkin, 2006, published in Geokhimiya, 2006, No. 10, pp. 1040–1052.     

电子探针与扫描电镜在翡翠饰品鉴别中的应用

利用电子探针、扫描电子显微镜对翡翠饰品进行表面形貌、物质组成的测定,结合偏光显微镜研究成果,以其微区、微量、无损、快速的特点,为翡翠饰品的鉴别提供了一种有效的方法和途径.     

Implications from inclusions in topaz for greisenisation and mineralisation in the Hensbarrow topaz granite, Cornwall, England

Textural and geochemical studies of inclusions in topaz from greisens in the Hensbarrow topaz granite stock (St. Austell, Cornwall) are used to constrain the composition of fluids responsible for late stage greisening and mineralisation. The topaz contains an abundant and varied suite of inclusions including aqueous liquid + vapour (L + V), quartz, zinnwaldite, albite, K-feldspar, muscovite, ilmenorutile, apatite, columbite, zircon, varlamoffite [(Sn, Fe)(O, OH)₂] and qitianlingite [(Fe⁺²,Mn⁺²)₂(Nb,Ta)₂W⁺⁶O₁₀]. Primary L + V inclusions in topaz show relatively high T _h (mainly 300 to >500 °C) and a narrow range of salinities (23–30 wt % NaCl equivalent) compared with those in greisen quartz (150–450 °C, 0–50 wt % NaCl equivalent). Textures indicate that topaz formed earlier than quartz and the fluid inclusion data are interpreted as indicating a cooling of the hydrothermal fluids during greisenisation, mixing with meteoric waters and a decrease in pressure causing intermittent boiling. The presence of early-formed albite and K-feldspar as inclusions in the topaz is likely to indicate that the greisen-forming fluid became progressively more acid during greisenisation. The most distinctive inclusions in the topaz are wisp- and bleb-shaped quartz, < 50 μm in size, which show textural characteristics indicating former high degrees of plasticity. They often have multiple shrinkage bubbles at their margins rich in Sn, Fe, Mn, S and Cl and, more rarely, contain euhedral albite, K-feldspar, stannite or pyrrhotite crystals up to 40 μm in size. The quartz inclusions show similar morphologies to inclusions in topaz from quartz-topaz rocks elsewhere which have been interpreted as trapped “silicate melt”. Their compositions are, however, very different to those expected for late stage topaz-normative granitic melts. From their textural and chemical characteristics they are interpreted as representing crystallised silica colloid, probably trapped as a hydro gel during greisenisation. There is also evidence for the colloidal origin of inclusions of varlamoffite in the topaz. These occurrences offer the first reported evidence in natural systems for the formation of colloids in high temperature hydrothermal fluids. Their high ore carrying potential is suggested by the presence of varlamoffite and the occurrence of stannite, pyrrhotite and SnCl within the quartz inclusions. Received: 9 April 1996 / Accepted: 12 November 1996     

Electron microscope study of the humite minerals: I. Mg-Rich specimens

Natural humite minerals and synthetic fluoro-humites, ideally described as nMg₂SiO₄ · Mg(OH,F)₂ (1<n<4), were investigated by using electron diffraction and imaging techniques. In clinohumite (n=4) and humite (n=3) irregularities in lattice spacings were observed parallel to (001). These were identified, using high resolution lattice images, as upper member lamellae in which n was always even (i.e., n=6, 8, 10 etc.). In fluoroclinohumite the higher members were sometimes perfectly ordered, giving rise to superstructures with relatively large c axes. These supercells always consisted of several consecutive unit cells of clinohumite (n=4) followed by a unit cell of the n=6 member; the largest observed had a d (001) spacing of 169 Å. It was also found that coherent intergrowths of massive portions of humite (n=3) and chondrodite (n=2) often occurred.     

Electron microscope study of the humite minerals: II. Mn-rich specimens

The results of an electron-microscope study of the alleghanyite (Mn-humite) minerals differ in some respects from those previously reported for the Mg-rich humites. They again reveal coherent intergrowths of the group members, but in some cases with very dense lamellar faulting, especially in alleghanyite specimens from the Benallt mine, Wales. Some of these faults were higher members of the series which occurred as very thin lamellae one or two unit cells thick. Superstructures (ordered intergrowths at the unit-cell level) were very rare; one, which was an ordered intergrowth of alternating bands of manganhumite and sonolite (Mn-clinohumite), was observed. Complex intergrowths at this level, but without translational periodicity, were more common. Such fragments were often twinned polysynthetically. Many specimens yielded relatively large crystal fragments of more than one member of the series (but without coherent boundaries). In some cases leucophoenicite was also present.     

Scanning electron microscope observation of dislocations in olivine

Dislocations in olivine decorated by oxidation in air were observed with a scanning electron microscope (SEM) using a backscattered electron image (BEI). The decorated dislocations (and grain boundaries) were found to give clear bright images in this mode, indicating an increase of mean atomic number near the dislocation cores (and grain boundaries). This method of dislocation observation has a resolution of ca. 0.1 μm, about an order of magnitude better than optical microscopic observation, and is particularly useful in the study of the overall dislocation distribution of naturally and experimentally deformed olivines with relatively high dislocation densities.     

Analytical electron microscope study of eight ataxites

Optical and electron optical (SEM, TEM, AEM) techniques were employed to investigate the fine structure of eight ataxite-iron meteorites. Structural studies indicated that the ataxites can be divided into two groups; a Widmanstätten decomposition group and a martensite decomposition group. The Widmanstätten decomposition group has a Type I plessite microstructure and the central taenite regions contain highly dislocated lath martensite. The steep M shaped Ni gradients in the taenite are consistent with the fast cooling rates, ≥500°C/my, observed for this group. The martensite decomposition group has a Type III plessite microstructure and contains all the chemical group IVB ataxites. The maximum taenite Ni contents vary from 47.5 to 52.7 wt% and are consistent with slow cooling to low temperatures ≤350°C at cooling rates ≤25°C/my. Ordered FeNi and the cloudy border structure were not observed in any of the ataxites. Modest reheating to ≤350°C may have been responsible for the lack of these structures.     

Water in minerals detectable by electron energy-loss spectroscopy EELS

Electron energy-loss spectroscopy EELS of the oxygen K edge of OH^– containing minerals and minerals with molecular water reveals a peak at about 528 eV prior to the onset of the O-K edge at 532 eV. This peak is never observed in minerals without water or OH^– groups. The intensity of the signal at 528 eV increases with increasing water content of the minerals. The peak at 528 eV is attributed to OH groups or water molecules. From the observations it is concluded that EELS provides a new method to determine the OH^– or water content of minerals with a spatial resolution far beyond that of optical spectroscopy. Received: 28 April 1997 / Revised, accepted: 25 July 1997     

浅论黄玉的成因与成岩-成矿模式

根据含黄玉岩石的矿物学、地质和地球化学以及黄玉中的流体包裹体特征研究，借鉴富F酸性岩体系的成岩成矿实验新成果，推出了新的黄玉成岩-成矿模式，力证黄玉是以富氟低熔岩浆结晶为主的多成因产物，不否定黄玉的交代蚀变和变质成因，认为盲目滥用和过分夸大变质（含交代）作用及其成岩、成矿的极端重要性和普适性不可取。     

Interpretation of the auger electron spectra (AES) of sulfide minerals

Auger electron spectra (AES) of sulfides are interpreted using published photoelectron spectra, sulfurK _β X-ray emission spectra (XES) and Multiple ScatteringX _α calculations on metal-sulfide molecular clusters and using newly measured spectra for ZnS, Cu₂S and MoS₂. For compounds without appreciable metald-sulfur 3p interactions, only one sulfur LVV peak or a closely spaced doublet is observed. For those with substantial metald-sulfur 3p interactions additional peaks occur, with peaks at lower electron kinetic energy arising from ejection of electrons from orbitals more tightly bound than theS3p, and those with higher kinetic energy arising from electrons in less tightly bound orbitals. Thus, for many sulfide minerals, the sulfur LVV Auger Spectrum is essentially a self-convolution of the valence band density of states weighted by the amount of S3p character, and can be predicted from a knowledge of the sulfurK _β X-ray emission spectra and the X-ray photoelectron spectra.     

Spectroscopic investigation and theoretical modeling of kaolinite-group minerals and other low-temperature phases

This article summarizes some recent results obtained on the physical properties of environmental minerals, mostly kaolinite-group minerals and Fe- and Al-(hydr)oxides occurring in lateritic soils. The defective structure of these minerals, including impurities, stacking faults and radiation-induced defects, is probed using infrared spectroscopy and electron paramagnetic resonance. Resulting information bears on models of soil formation and transformation mechanisms of minerals in low-temperature environments. We underline the increasing impact of quantum chemical modeling in this field, providing straightforward interpretations of spectroscopic signals and overcoming the limits of fingerprint approaches. Importantly, the first-principles modeling of isotopic fractionation factors provides new links between mineralogical and geochemical investigations of secondary minerals.     

基于深度学习的镜下矿石矿物的智能识别实验研究

矿石矿物鉴定的智能化是智能地质学和智能矿床学的基础技术之一。计算机视觉技术和深度学习理论使矿石矿物鉴定的智能化成为可能。本研究基于深度学习系统Tensor Flow,以吉林夹皮沟金矿和河北石湖金矿的黄铁矿、黄铜矿、方铅矿、闪锌矿等硫化物矿物为例,设计有针对性的Unet卷积神经网络模型,有效自动提取矿相显微镜下矿石矿物的深层特征信息,实现镜下矿石矿物智能识别与分类。实验显示,模型在训练过程中,随着训练次数的增加,模型精度在不断增大,损失函数不断减小;经过3000个批处理之后,模型精度和损失函数基本趋于稳定。训练出的模型对测试集中的显微镜镜下矿石矿物照片的识别成功率均高于90%,说明实验所建立的模型,具有很好的图像特征提取能力,能完成镜下矿石矿物智能识别的任务。     

A transmission electron microscope study of naturally deformed orthopyroxene

A model is proposed for the production of clinopyroxene lamellae in orthopyroxene by a dislocation mechanism based on simple shear. Four possible shears are described. Two shears apply to each subcell of orthopyroxene, one with =13.3° in one sense, the other with =18.3° in the opposite sense.The senses of shears of the same magnitude in adjacent cells are also opposite. All shears produce the same structure, but in two discrete orientations which can be distinguished from electron diffraction patterns. However, the operative shear cannot be uniquely determined from the diffraction patterns alone. The characteristics of the diffraction contrast fringes and associated partial dislocations observed by transmission electron microscopy in a naturally deformed orthopyroxene are shown to be consistent with the proposed model.     

Universal stage measurements and transmission electron microscope observations of fractured plagioclase

At low to moderate temperatures of deformation, fracturing of plagioclase is common. The mechanism of fracturing is generally thought to be either a dislocation assisted process with fractures typically exhibiting some crystallographic regularity or a process of breaking along cleavage planes without the involvement of dislocations. In this study, naturally fractured plagioclase from granodiorites and a gabbro deformed at high strain rates are examined with the transmission electron microscope (TEM) to identify structures at that scale. In addition, fracture orientations are determined with the Universal stage.Some fractures observed in thin section occur parallel to (001) but many are not so simple but are confined to the [112], [1$\text{1}$2], [101], [$\text{1}$01] zones. At the TEM scale, dislocation walls or arrays are common in plagioclase. They also occupy the [101], [$\text{1}$01], [112], [1$\text{1}$2] zones. Microcracks form when dislocations are pinned in these arrays or when a free dislocation interacts with dislocations within a dislocation wall. In this way, large-scale fractures which develop inherit their crystallographic orientation from the dislocation wall.     

Clays and other minerals in coal seams of the Moura-Baralaba area, Bowen Basin, Australia

The clays and other minerals in a succession of Late Permian coals of high-volatile bituminous to semi-anthracite rank have been identified, using low-temperature oxygen plasma ashing and X-ray diffraction, and evaluated to identify the relative roles in mineral matter formation of detrital input, early diagenesis in the peat swamp and late diagenesis associated with rank advance. Although well-ordered kaolinite of probable early diagenetic origin is abundant throughout the succession, the uppermost and lowermost seams of the sequence, regardless of rank, contain relatively abundant illite and/or interstratified illite/smectite, along with a small but significant proportion of chlorite. These clays are thought to be essentially of detrital origin, washed or blown into the peat deposit in relative abundance during the establishment and subsequent overwhelming of an extensive and long-lived swampy environment. Quartz is also abundant in the lower seams of the sequence, especially close to the regional sediment source area. Illite is unusually abundant in the topmost seam in both high- and low-rank parts of the succession, and thus appears to represent detrital input from a particular source material. Although significant changes are reported in the clays of the associated strata due to rank advance, the principal effect of rank advance on the minerals in the coal itself appears to be the development of an ammonium illite, and possibly some additional fine-grained chlorite, in the semi-anthracite material. Isolation within the organic matter of the coal is thought to have inhibited access for ions such as K⁺, which might otherwise have become involved in metamorphic reactions and given rise to mineralogical changes commonly found in non-coal sedimentary successions.     

Amphibolites with staurolite and other aluminous minerals: calculated mineral equilibria in NCFMASH

Amphibolite facies mafic rocks that consist mainly of hornblende, plagioclase and quartz may also contain combinations of chlorite, garnet, epidote, and, more unusually, staurolite, kyanite, sillimanite, cordierite and orthoamphiboles. Such assemblages can provide tighter constraints on the pressure and temperature evolution of metamorphic terranes than is usually possible from metabasites. Because of the high variance of most of the assemblages, the phase relationships in amphibolites depend on rock composition, in addition to pressure, temperature and fluid composition. The mineral equilibria in the Na₂O–CaO–FeO–MgO–Al₂O₃–SiO₂–H₂O (NCFMASH) model system demonstrate that aluminium content is critical in controlling the occurrence of assemblages involving hornblende with aluminous minerals such as sillimanite, kyanite, staurolite and cordierite. Except in aluminous compositions, these assemblages are restricted to higher pressures. The iron to magnesium ratio (X_Fe), and to a lesser extent, sodium to calcium ratio, have important roles in determining which (if any) of the aluminous minerals occur under particular pressure–temperature conditions. Where aluminous minerals occur in amphibolites, the P–T–X dependence of their phase relationships is remarkably similar to that in metapelitic rocks. The mineral assemblages of Fe‐rich amphibolites are typically dominated by garnet‐ and staurolite‐bearing assemblages, whereas their more Mg‐rich counterparts contain chlorite and cordierite. Assemblages involving staurolite–hornblende can occur over a wide range of pressures (4–10 kbar) at temperatures of 560–650 °C; however, except in the more aluminous, iron‐rich compositions, they occupy a narrow pressure–temperature window. Thus, although their occurrence in ‘typical’ amphibolites may be indicative of relatively high pressure metamorphism, in more aluminous compositions their interpretation is less straightforward.