Impurity Elements in Quartz from Gold Deposits of the Darasun Ore Field (Eastern Transbaikalia,Russia): Electron Paramagnetic Resonance Data

The distribution of substitutional Al, Ti, and Ge impurities in quartz samples from the Darasun, Teremkinskoe, and Talatui gold deposits, located in the Darasun ore field, were studied by electron paramagnetic resonance. The relationship between the isomorphous substitution and dynamic recrystallization of quartz was studied by optical and scanning electron microscopy. It was found that analysis of the plots of interdependence between the concentrations of various substitutional impurities in quartz (isogens) can detect development trends of isomorphous substitution. Two isomorphous substitution stages were recognized, one associated with quartz crystallization, and the other, with its subsequent dynamic recrystallization. The first stage is characterized by incorporation of Al impurity into the quartz crystal lattice, and the second, by incorporation Ti impurity. A Ge impurity is a catalyst for isomorphous substitution, and its concentrations vary widely. It is noted that the second stage plays a decisive role, because it accounts for the incorporation of the larger part of substitutional impurities. This process is facilitated by the dynamic recrystallization of quartz. Four genetic quartz groups, described by individual isogens, have been recognized in the Darasun ore field. Two of them correspond to quartz crystallized directly from a magmatogenic fluid or redeposited with the melt’s participation, and the other two groups, to quartz crystallized from an altered fluid. It was found that substitutional Al concentrations are retained in quartz after redeposition, whereas substitutional Ti concentrations decrease dramatically Mineral formation processes at each gold deposit are reviewed. Two types of temperature zoning, normal and reverse, have been recognized at the Darasun deposit. Each is characterized by an individual genetic quartz group and the degree of closedness of the mineral formation system. The genetically similar magmatogenic quartz samples found at the Darasun and Talatui deposits indicate the uniformity of the mineralization process in the Darasun ore field. The established trends of isomorphous substitution in quartz are useful in studies of the ore formation histories of gold and other ore deposits.

     

Genetic analysis of quartz from pegmatites of the Mama-Chuya mica belt based on distribuition of isomorphic impurities, Russia

The effect of the formation conditions of pegmatites in the Mama-Chuya mica belt on the distribution of isomorphic Al, Ti, and Ge impurities in quartz detected by electron paramagnetic resonance (EPR) has been estimated using the isogen method, which takes into account the relationship between this distribution and geological time. It has been revealed that each of the studied types of pegmatite veins is described by special isogens that reflect interrelations between concentrations of various isomorphic impurities. The typification of veins, enrichment of parental melt in water, and other factors affect the isogens. New potentialities of the isogen method for genetic analysis of quartz have been established.     

南秦岭安康地区高纯石英用脉石英矿特征及质量影响因素

南秦岭安康地区志留系梅子垭组千枚岩中赋存丰富的脉石英矿产资源, 但其作为高纯石英原料研究程度低, 尤其是对其中影响石英提纯的痕量杂质元素含量及其赋存状态缺乏系统认识, 很大程度制约了该区高纯石英原料的质量评价和进一步的找矿突破。本文在厘定安康地区脉石英地质发育特征的基础上, 对研究区产出的3件脉状石英样品(AK200、AK201、AK202)开展了样品杂质元素检测, 对样品矿物学特征、杂质赋存形式和可提纯性能进行了研究, 进而进行了提纯实验, 结果显示, 3件样品提纯后SiO₂含量分别为99.993 11%、99.997 66%和99.998 58%, 均达到高纯石英产品质量要求, 其中AK202样品提纯后达到4N8级。研究表明, 提纯后Al、Ti、Na、K为主要杂质元素, Al可能以杂质矿物、晶格杂质两种方式存在; Ti可能多以晶格杂质的方式存在; Na、K多以流体包裹体的方式存在; 杂质矿物、流体包裹体、晶格杂质对该区脉石英质量均产生不同程度影响, 其中流体包裹体为主要影响因素, 晶格杂质次之, 杂质矿物影响最小。这一结论对于评价该区的脉石英矿产资源质量、明确今后找矿目标体特征具有重要参考意义。     

高纯石英的研究进展及发展趋势

石英是一种在地壳上大量分布,有着广泛工业用途和广阔应用前景的矿物。当石英晶体形成演化时,受结晶时环境条件、流体性质、结晶后遭受改造(如变质作用、构造变形和热扰动等)等影响,杂质元素如P、Ti、Ge、Al、B、Be、Ca、Na、K、H、Li等会或多或少存在于石英晶体中,因此在自然界不存在纯SiO₂组分的石英。同时,基于石英的微量元素组成,可以反演石英源区和形成演化过程,并用于研究岩石及矿床成因等科学问题。石英晶体内部杂质元素以类质同象替代、气液包裹体、矿物包裹体(不能按尺度分,应该按照状态划分存在形式)3种形式存在。石英中杂质元素的种类、含量、赋存形式,特别是包裹体特征将直接影响石英资源的品质和工业用途。本文还系统地阐述了石英的发光特性、工艺性能以及高纯石英的质量分类与标准和高纯石英原料来源等方面的内容。在本研究中,通过光学显微镜和激光拉曼测试,初步地查明了苏北张锦庄石英砂和广西姑婆山花岗岩石英中流体包裹体的分布和矿物包裹体的种类,这是开展后续研究的基础。高纯石英是优质石英资源经纯化加工得到的高品质石英原材料,可用于石英玻璃、石英坩埚、半导体、高温灯管、光纤、精密光学、微电子和太阳能等高新技术产业中。研究高纯石英原料的评价体系、理想源岩和形成机制有益于持续性地供给高纯石英原料, 极大地提高了石英原料的工业附加值。     

载金石英的化学成分特征及其意义

利用电子显微镜(EM)及能谱仪(EDS),分析研究了变生热液形成的载金石英的化学成分、离子扩散作用以及金在石英中的赋存状态等问题,探讨了它们的形成和变化机理。研究结果表明:Al~(3+)、Ti~(3+)、TFe、Na~(+)、K~(+)、Ca~(2+)等在石英中为类质同像混入物;石英和黄铁矿之间的离子相互扩散作用,表现为石英中Al离子的带出和Fe离子的带入,黄铁矿中Fe离子的带出和Al离子的带入;石英中呈分散状态分布的金主要为离子金,它们充填在石英结构中,起平衡电价的作用。     

Quartz chemistry – A step to understanding magmatic-hydrothermal processes in ore-bearing granites: Cínovec/Zinnwald Sn-W-Li deposit,Central Europe

Quartz from granites, greisens and quartz veins from a 1596 m long vertical section through the Cínovec/Zinnwald Li-Sn-W deposit (Czech Republic) was studied using cathodoluminescence (CL) and laser ablation inductively coupled plasma mass spectrometry (LA-ICP MS). The trace contents of Al, Ti, Li and the Ge/Ti and Al/Ti values in quartz reflect the degree of fractionation of parental melt from which primary quartz crystallized. From the biotite granite to the younger zinnwaldite granite, quartz is characterized by increasing contents of Al (from 136–176 to 240–280 ppm) and decreasing Ti (from 16–54 to 6–14 ppm), while the contents of Li and Ge are similar (15–36 and 0.8–1.7 ppm, respectively). Quartz of the greisen stage and vein stage is poor in all measured elements (26–59 ppm Al, 0.5–1.6 ppm Ti, 2–13 ppm Li, 0.8–1.6 ppm Ge). The youngest low-temperature quartz forming thin coatings in vugs in greisen and veins differs in its extreme enrichment in Al (>1000 ppm) and Li (∼100 ppm) and very low Ti (<1 ppm). Within the greisen, remnants of primary magmatic quartz should be distinguished from metasomatic greisen-stage quartz in their higher intensity of CL and relatively higher Ti contents. A part of primary magmatic quartz may by secondarily purified via infiltration of hydrothermal fluids and dissolution–reprecipitation processes. Such quartz parallels newly formed greisen-stage quartz in its chemical and CL properties; the share of greisen-stage quartz may by therefore overestimated.     

Distribution and petrogenetic behaviour of trace elements in granitic pegmatite quartz from South Norway

The present study documents that the trace-element distribution in granitic quartz is highly sensitive to CAFC processes in granitic melts. Igneous quartz efficiently records both the origin and the evolution of the granitic pegmatites. Aluminium, P, Li, Ti, Ge and Na in that order of abundance, comprises >95% of the trace elements. Most samples feature >1 ppm of any of these elements. The remnant 5% includes K, Fe, Be, B, Ba and Sr whereas the other elements are present at concentrations lower than the detection limit. Potassium, Fe, Be and Ti are relatively compatible hence obtain the highest concentrations in early formed quartz. Phosphorous, Ge, Li and Al are relatively incompatible and generally obtain the highest concentrations in quartz that formed at lower temperatures from more evolved granitic melts. The Ge/Ti, the Ge/Be, the P/Ge and the P/Be ratios of quartz are strongly sensitive to the origin and evolution of the granitic melts and similarly the Rb/Sr and the Rb/K ratios of K-feldspars may be utilised in petrogenetic interpretations. However, the quartz trace element ratios are better at distinguishing similarities and differences in the origin and evolution of granitic melts. After evaluating the different trace element ratios, the Ge/Ti ratio appears to be most robust during subsolidus processes in the igneous systems, hence probably should be the preferred ratio for analysing and understanding petrogenetic processes in granitic igneous rocks.Editorial responsibility: J. Hoefs     

Trace element incorporation into quartz: A combined study by ICP-MS, electron spin resonance, cathodoluminescence, capillary ion analysis, and gas chromatography

Pegmatite quartz from different occurrences in Norway and Namibia was investigated by a combination of ICP-MS, Electron Spin Resonance (ESR), Capillary Ion Analysis (CIA) and Gas Chromatography (GC) to quantify trace elements in very low concentrations and to determine their position in the quartz structure.The studied quartz samples show similar geochemical characteristics with low contents of most trace elements. Remarkable are the elevated concentrations of Al (36-636 ppm), Ti (1.6-25.2 ppm), Ge (1.0-7.1 ppm), Na (5.2 to >50 ppm), K (1.6 to >100 ppm) and Li (2.1-165.6 ppm). These elements are preferentially incorporated into the quartz lattice on substitutional (Al, Ti, Ge) and interstitial (Li, Na, K) positions. Li⁺ was found to be the main charge compensating ion for Al, Ge and Ti, whereas some ppm of Na and K may also be hosted by fluid inclusions. Ti may be incorporated as substitutional ion for Si or bound on mineral microinclusions (rutile). The results of the ESR measurements show that there may be a redistribution of alkali ions during irradiation. The diamagnetic [AlO₄/M⁺]⁰ center transforms into the paramagnetic [AlO₄]⁰ center, whilst the compensating ions diffuse away and may be captured by the diamagnetic precursor centers of [GeO₄]⁰ and [TiO₄]⁰ to form paramagnetic centers ([TiO₄/Li⁺]⁰, [GeO₄/Li⁺]⁰).In general, fluid inclusions in pegmatite quartz can be classified as H₂O-CO₂-NaCl type inclusions with water as the predominant volatile. Among the main elements hosted by fluid inclusions in quartz are Na, K, NH₄, Ca, Mg and the anionic complexes Cl⁻, NO₃⁻, HCO₃⁻ and SO₄²⁻. Gas analysis of trapped fluids shows volatile components in the following order of abundance: H₂O > CO₂ > N₂(+) ≥ CH₄ > COS > C₂ and C₃ hydrocarbons. Additionally, traces of Co, Ni, Zn, Pb, and Cu were detected by CIA in fluid inclusions of some samples. There are indications that the REE and Rb are also bound in fluid inclusions, however, the concentrations of these elements are too low to be measured by CIA. Assuming that the REE preferentially occur in fluid inclusions, the typical chondrite normalized REE distribution patterns with tetrad effects and a distinct negative Eu anomaly would reflect the composition of the mineralizing fluid.For a number of elements, especially those with extremely low concentrations, the “type” of incorporation in quartz could not directly be determined. We conclude that these ions either are too large to substitute for the small Si⁴⁺ ion or they are not soluble in the mineralizing fluids to be hosted by fluid inclusions. Some of these elements, which are concentrated in the specific mineralization of certain pegmatites, are not present in elevated concentrations in the paragenetic pegmatite quartz itself. This was observed, for instance, for Be, Cs and Rb in the Li (Be-Cs-Rb) pegmatites of Rubicon or for Nb and Ta for Nb-Ta bearing pegmatites from Norway. It may be concluded that the concentrations of these trace elements in quartz do not reflect the mineralization and that these elements thus, cannot be used as petrogenetic indicator.     

Structural defects and polymorphic transformations in quartz

The influence of structural defects on the polymorphic transformations in quartz was studied by electron paramagnetic resonance and electron microscopy. It was established that the kinetics of the accumulation of the clusters of the β-phase depends on isomorphic impurities in quartz. It was confirmed that germanium ions and vacancies in quartz participate in the formation of the clusters. Obtained results allow the assumption that the amount of germanium required to preserve clusters increases with increasing temperature and vice versa. An explanation is presented for experimentally observed decomposition of clusters during artificial heating of some quartz samples. It was found that the clusters of the β-phase are autonomous units, i.e. may exist independently of host crystalline structure of quartz. The possible mechanism of influence of Ge impurity on the temperature of α-β-transition in quarts is discussed.     

Minor elements in quartz from hydrothermal-metamorphic veins in the Nether Polar Ural Province

Vein quartz from the Nether Polar Ural Province was examined by atomic emission spectrometry, gas chromatography, electron paramagnetic resonance, and electron microscopy. According to atomic emission spectrometric analysis, the total concentration of Al, Fe, Mg, Ti, Ca, Na, K, and other minor elements in the quartz varies from 8 to 47 ppm. The lowest concentrations of minor elements were detected in the granulated quartz. Giant-crystalline milk-white quartz is noted for higher concentrations of minor elements, including Na, K, and Ca, because it contains gas-liquid inclusions. The fine-grained quartz contains very small mineral inclusions and is thus noted for elevated concentrations of Ca, Fe, K, Mg, and Ti. Gas chromatographic data on the gas phase separated from the quartz at its heating indicate that this phase contains H₂O, CO₂, and other components. The H₂O concentration reaches 429 ??g/g, while the CO₂ content is commonly no higher than 20 ??g/g. Gas separation is at a maximum at temperatures of 100?C600°C, when gasliquid inclusions decrepitate, as is typical, first of all, of the giant-crystalline milk-white quartz. Gas separation continues at higher temperatures (below 1000°C) but is much less intense. The electron microscopic examination of quartz grains after their acid treatment indicates that the surface of these grains is covered by caverns of various morphology and size, which were produced by the partial dissolution of the quartz and the opening of its gas-liquid and mineral inclusions occurring near the surface; the inclusions were not, however, completely removed. The crystal structure of the quartz contains minor Al, Ge, Na, Li, Ti, and Fe. The lowest concentrations of Al and Ge paramagnetic centers are typical of the granulated (recrystallized) and fine-grained quartz. The giant-crystalline quartz, including its transparent varieties, and individual quartz crystals, first of all their smoky-citrine varieties, contain higher concentrations of minor elements. In the Nether Polar Ural Province, granulated quartz is potentially promising for producing especially pure quartz concentrates. The quality of the translucent coarse-to giant-crystalline quartz, which predominates in the resources and reserves, is deteriorated by gas-liquid inclusions in it and requires deep processing of the raw minerals.     

Germanium-silicon fractionation in a tropical, granitic weathering environment

Germanium-silicon (Ge/Si) ratios were determined on quartz diorite bedrock, saprolite, soil, primary and secondary minerals, phytolith, soil and saprolite pore waters, and spring water and stream waters in an effort to understand Ge/Si fractionation during weathering of quartz diorite in the Rio Icacos watershed, Puerto Rico. The Ge/Si ratio of the bedrock is 2 μmol/mol, with individual primary mineral phases ranging between 0.5 and 7 μmol/mol. The ratios in the bulk saprolite are higher (∼3 μmol/mol) than values measured in the bedrock. The major saprolite secondary mineral, kaolinite, has Ge/Si ratios ranging between 4.8 and 6.1 μmol/mol. The high Ge/Si ratios in the saprolite are consistent with preferential incorporation of Ge during the precipitation of kaolinite. Bulk shallow soils have lower ratios (1.1-1.6 μmol/mol) primarily due to the residual accumulation of Ge-poor quartz.Ge/Si ratios measured on saprolite and soil pore waters reflect reactions that take place during mineral transformations at discrete depths. Spring water and baseflow stream waters have the lowest Ge/Si ratios (0.27-0.47 μmol/mol), reflecting deep initial weathering reactions resulting in the precipitation of Ge-enriched kaolinite at the saprolite-bedrock interface. Mass-balance calculations on saprolite require significant loss of Si and Al even within 1 m above the saprolite-bedrock interface. Higher pore water Ge/Si ratios (∼1.2 μmol/mol) are consistent with partial dissolution of this Ge-enriched kaolinite. Pore water Ge/Si ratios increase up through the saprolite and into the overlying soil, but never reach the high values predicted by mass balance, perhaps reflecting the influence of phytolith recycling in the shallow soil.     

High-purity quartz mineralisation in kyanite quartzites,Norway

This study presents an evaluation of Norwegian kyanite quartzites from Gullsteinberget, Knøsberget, Kjeksberget, Sormbrua, Tverrådalen, Juovva?orrú and Nasafjellet as potential deposits of high-purity quartz (HPQ) for use as raw material for special applications in high-technology industries. Fine-grained quartz, which forms 70 to 85 vol.% of these rocks, generally contains less than 50 μg g^?1 (total sum) of the structurally incorporated trace elements B, Li, Al, Ge, Ti, Fe, Mn, K and P. The concentrations are in the same range as those found in HPQ products, which are being mined and produced in Norway and elsewhere. Quartz analyses were performed using laser ablation–inductively coupled plasma mass spectrometry. Complimentary whole-rock analyses and cathodoluminescence studies of quartz were carried out to reveal processes, which have led to the low trace-element concentrations in quartz. This discovery, together with a better knowledge of the processes leading to the formation of HPQ in kyanite quartzites, could lead to the recognition of a new global type of HPQ resource applicable for industrial use. However, the processing technology necessary to separate HPQ from kyanite quartzite economically has not been developed so far.     

Ca- and Mg-perovskite phases in the Earth’s mantle as a probable reservoir of Al: Computer-simulation evidence

Semi-empirical and quantum chemical studies of Al atom energy in CaSiO₃ and MgSiO₃ with the perovskite-type structure at pressures and temperatures of the Earth’s mantle are reported. The phase diagram for CaSiO₃ is reproduced and refined. Probable mechanisms of Al incorporation in the structures studied are considered. According to the results of the calculations, Al is preferably incorporated into MgSiO₃, rather than into CaSiO₃. Evaluation of the isomorphic capacity of perovskite phases in relation to Al shows that the Al content in MgSiO₃ may reach 2.4 mol % at 120 GPa and 2400 K. CaSiO₃ cannot be a source of Al atoms in the Earth’s mantle.     

Mineral and inorganic chemical composition of the Pernik coal, Bulgaria

The mineral and inorganic chemical composition of five types of samples from the Pernik subbituminous coals and their products generated from the Pernik preparation plant were studied. They include feed coal, low-grade coal, high-grade coal, coal slime, and host rock. The mineral matter of the coals contains 44 species that belong mainly to silicates, carbonates, sulphates, sulphides, and oxides/hydroxides, and to a lesser extent, chlorides, biogenic minerals, and organic minerals. The detrital minerals are quartz, kaolinite, micas, feldspars, magnetite, cristobalite, spessartine, and amphibole. The authigenic minerals include various sulphides, silicates, oxihydroxides, sulphates, and carbonates. Several stages and substages of formation were identified during the syngenetic and epigenetic mineral precipitations of these coals. The authigenic minerals show the greatest diversity of mineral species as the epigenetic mineralization (mostly sulphides, carbonates, and sulphates) dominates qualitatively and quantitatively. The epigenetic mineralization was a result of complex processes occurring mostly during the late development of the Pernik basin. These processes indicate intensive tectonic, hydrothermal and volcanic activities accompanied by a change from fresh to marine sedimentation environment. Thermally altered organic matter due to some of the above processes was also identified in the basin. Most of the trace elements in the Pernik coals (Mo, Be, S, Zr, Y, Cl, Ba, Sc, Ga, Ag, V, P, Br, Ni, Co, Pb, Ca, and Ti) show an affinity to OM and phases intimately associated with OM. Some of the trace elements (Sr, Ti, Mn, Ba, Pb, Cu, Zn, Co, Cr, Ni, As, Ag, Yb, Sn, Ga, Ge, etc.) are impurities in authigenic and accessory minerals, while other trace elements (La, Ba, Cu, Ce, Sb, Bi, Zn, Pb, Cd, Nd, etc.) occur as discrete phases. Elements such as Sc, Be, Y, Ba, V, Zr, S, Mo, Ti, and Ga exceed Clarke concentrations in all of the coal types studied. It was also found that a number of elements in the Pernik coals (F, V, As, Pb, Mo, Li, Sr, Ti, Ga, Ni, Ge, Cr, Mn, etc.) reveal mobility in water and could have some environmental concerns.     

The effect of deformation on the TitaniQ geothermobarometer: an experimental study

We performed high strain (up to 47 %) axial compression experiments on natural quartz single crystals with added rutile powder (TiO₂) and ~0.2 wt% H₂O to investigate the effects of deformation on the titanium-in-quartz (TitaniQ) geothermobarometer. One of the objectives was to study the relationships between different deformation mechanisms and incorporation of Ti into recrystallized quartz grains. Experiments were performed in a Griggs-type solid-medium deformation apparatus at confining pressures of 1.0–1.5 GPa and temperatures of 800–1,000 °C, at constant strain rates of 1 × 10^?6 or 1 × 10^?7 s^?1. Mobility of Ti in the fluid phase and saturation of rutile at grain boundaries during the deformation experiments are indicated by precipitation of secondary rutile in cracks and along the grain boundaries of newly recrystallized quartz grains. Microstructural analysis by light and scanning electron microscopy (the latter including electron backscatter diffraction mapping of grain misorientations) shows that the strongly deformed quartz single crystals contain a wide variety of deformation microstructures and shows evidence for subgrain rotation (SGR) and grain boundary migration recrystallization (GBMR). In addition, substantial grain growth occurred in annealing experiments after deformation. The GBMR and grain growth are evidence of moving grain boundaries, a microstructure favored by high temperatures. Electron microprobe analysis shows no significant increase in Ti content in recrystallized quartz grains formed by SGR or by GBMR, nor in grains grown by annealing. This result indicates that neither SGR nor moving grain boundaries during GBMR and grain growth are adequate processes to facilitate re-equilibration of the Ti content in experimentally deformed quartz crystals at the investigated conditions. More generally, our results suggest that exchange of Ti in quartz at low H₂O contents (which may be realistic for natural deformation conditions) is still not fully understood. Thus, the application of the TitaniQ geothermobarometer to deformed metamorphic rocks at low fluid contents may not be as straightforward as previously thought and requires further research.     

Cathodoluminescence and micro-structural evidence for crystallisation and deformation processes of granites in the Eastern Lachlan Fold Belt (SE Australia)

Trace elements (Al, K, Ti, Fe), growth and deformation pattern in quartz of the multiple deformed Carcoar, Barry and Sunset Hills granites were investigated by electron micro probe and cathodoluminescence. Zoned quartz phenocrysts with high Ti concentrations (>70 ppm) that show blue cathodoluminescence originated from the early stage of magma crystallisation. Multiple deformation of quartz causes the redistribution of Al and K in the quartz lattice, which results in the accumulation of these elements in submicroscopic inclusions (<0.5 µm) of muscovite-like composition. In contrast, structural Ti in quartz is mostly kept in the lattice. Common halos of defect-poor, secondary quartz around fluid inclusions result from re-equilibration of fluid inclusions because of differences between fluid pressure and lithostatic pressure, e.g. during uplift (isothermal decompression) and/or !/#-transition of quartz. During healing, defect-poor secondary quartz grows at the cost of the host quartz and releases or replaces defect centres. The results of micro-structural investigations combined with Al-in-hornblende thermobarometry allow the reconstruction of regional processes. Carcoar and Barry granodiorites and Sunset Hills granite were intruded in the Late Ordovician-Early Silurian at depths of 4-8.6 and 10-12 km, respectively. In contrast to the continuous crystallisation of the granodiorite magmas, the magma of the Sunset Hills granite ascended in a stepwise fashion, causing multiple quartz nucleation. The two granodiorites were multiple, post-magmatically deformed, first, during Early Devonian under more brittle conditions at temperatures of 350-400 °C, whereas the Sunset Hills granite experienced more ductile deformation at temperatures of around 550 °C.     

OH defects in quartz in the system quartz–albite–water and granite–water between 5 and 25?kbar

The incorporation of OH defects in quartz from the systems quartz–water, quartz–albite–water and granite–water at pressures between 5 and 25?kbar and temperatures between 800 and 1,000?°C was investigated by IR spectroscopy. The two most important OH absorption features can be assigned to hydrogarnet defects (absorption band at 3,585?cm^?1) and coupled substitutions involving Al³⁺ (Al–H defects, absorption bands at 3,310, 3,378 and 3,430?cm^?1). Al incorporation in quartz is controlled by mineral/melt partitioning (D _Al ^Qz/Melt ?=?0.01) and exhibits a negative pressure dependence. This trend is not clearly reflected by the concentration of Al–H defects, which shows positive deviations from the theoretical 1:1 correlation of Al/H for some samples. In contrast to the Al–H defects, formation of hydrogarnet defects appears to be positively correlated to pressure and water activity, and may be used a petrological indicator. The overall water concentration exhibits only minor changes with pressure and temperature, but a clear correlation of water activity (controlled by various amounts of dissolved salts) and hydrogarnet substitution could be established.     

Contrasted modes of amphibole development in coronitic metagabbros: a TEM investigation

A TEM investigation of amphibole development in granulitic metagabbros is presented. Three different sites of amphibole nucleation and growth are observed: (i) in the clinopyroxene-plagioclase interphase boundaries, corresponding to a reconstructive transformation involving intercrystalline diffusion; (ii) along pyroxene fractures, with competition between inter- and intracrystalline diffusion; (iii) within the pyroxene crystals, through a topotactic conversion, controlled by intracrystalline diffusion. These different reaction sites are studied in order to discuss some aspects of reaction mechanisms within undeformed metamorphic rocks, putting into balance intracrystalline versus intercrystalline processes. According to the possible paths (crystal lattice and its defects, fractures and mineral interfaces), contrasted amounts of reaction products, together with different amphibole compositions are evidenced. These results indicate that the diffusion rate of Al, Fe, Mg and OH is the rate controlling factor for amphibole-forming reaction.     

Characterisation of a Natural Quartz Crystal as a Reference Material for Microanalytical Determination of Ti,Al, Li,Fe, Mn,Ga and Ge

A natural smoky quartz crystal from Shandong province, China, was characterised by laser ablation ICP‐MS, electron probe microanalysis (EPMA) and solution ICP‐MS to determine the concentration of twenty‐four trace and ultra trace elements. Our main focus was on Ti quantification because of the increased use of this element for titanium‐in‐quartz (TitaniQ) thermobarometry. Pieces of a uniform growth zone of 9 mm thickness within the quartz crystal were analysed in four different LA‐ICP‐MS laboratories, three EPMA laboratories and one solution‐ICP‐MS laboratory. The results reveal reproducible concentrations of Ti (57 ± 4 μg g^?1), Al (154 ± 15 μg g^?1), Li (30 ± 2 μg g^?1), Fe (2.2 ± 0.3 μg g^?1), Mn (0.34 ± 0.04 μg g^?1), Ge (1.7 ± 0.2 μg g^?1) and Ga (0.020 ± 0.002 μg g^?1) and detectable, but less reproducible, concentrations of Be, B, Na, Cu, Zr, Sn and Pb. Concentrations of K, Ca, Sr, Mo, Ag, Sb, Ba and Au were below the limits of detection of all three techniques. The uncertainties on the average concentration determinations by multiple techniques and laboratories for Ti, Al, Li, Fe, Mn, Ga and Ge are low; hence, this quartz can serve as a reference material or a secondary reference material for microanalytical applications involving the quantification of trace elements in quartz.     

橄榄石中H的结合机制及扩散行为

名义上无水矿物(nominally anhydrous minerals,NAMs)中以点缺陷形式存在的结构水,因其对于矿物物理化学性质的显著影响而受到越来越广泛的关注。橄榄石是上地幔中含量最丰富的矿物,水在橄榄石中的存在形式、扩散机制和速率对上地幔的流变学和电导性质有着重要的影响。因此,对于橄榄石中H的结合机制及其扩散机制和速率的了解有助于理解地球深部的水循环,也有助于构建上地幔流变结构以及解释电导测量结果。本文总结了近几十年来学界对于H在橄榄石中存在的缺陷类型与OH红外光谱吸收峰之间的对应关系,以及H在矿物晶格中的扩散机制、扩散速率等重要问题的研究成果,并探讨了现有研究中依然存在的问题。