Search Results (21)

Berthierine was found in a natrolite vein intersecting volcanogenic-sedimentary rocks on the slope of Mt. Quamdespakh in the upper reaches of the Suolwai River, Lovozero alkaline massif, Kola peninsula, Russian Arctic. The mineral occurs as well-formed translucent pyramidal crystals up to 250 μm in size. The chemical composition determined by electron microprobe analysis corresponds to the empirical formula ^VI(Fe²⁺_1.99Al_0.94Mg_0.03Mn_0.04)_Σ3.00[^IV(Si_1.15Al_0.85)_Σ2.00O₅] [(OH)_3.92O_0.08]_Σ4.00; the idealized formula is ^VI(Fe²⁺₂Al)[^IV(SiAl)O₅](OH)₄. The crystal-structure determination (the first detailed crystal-structure characterization of berthierine) shows that the Lovozero mineral is hexagonal, P6₃cm (a = 5.3903(4), c = 14.0146(10) Å, V = 352.64(6) ų, R₁ = 0.053 for 338 unique observed reflections), and corresponds to the 2H₁ polytype of serpentine-group minerals with 1:1 tetrahedral-octahedral layers. The unit cell contains two M₃[T₂O₅](OH)₄ layers (M = Fe²⁺,Al; T = Si,Al) stacked along the c axis. The calculations of information-based structural and topological complexity parameters indicate that berthierine is structurally and topologically simpler than its chlorite-group polymorph chamosite. Since berthierine usually crystallizes metastably in the stability field of chamosite, the complexity analysis is agreement with the Goldsmith rule that states that, in Ostwald sequences of crystallization, metastable phases are simpler and more disordered than their stable counterparts. This observation can be applied to a general case of the metastable formation of serpentine-group minerals prior to the crystallization of chlorites. Full article

The tremolite nephrite deposit in Dahua county, Hechi City, Guangxi province, China is a new genetic type of nephrite deposit. It is hosed by Mg-poor limestone (~1.30 wt.% MgO) and intruded by diabase (~45 wt.% SiO₂). The Mg and Si contents of these rocks are lower than those of the tremolite (58.18 wt.% SiO₂, 13.18 wt.% CaO, 24.16 wt.% MgO), indicating an obviously insufficient source for the metallogenic material that generated the deposit. In particular, some tremolite nephrite ore bodies have no clear contact metamorphism between the host and intrusive rocks, which have the characteristics of stratified mineralization (stratified tremolite nephrite). The origin and mineralization of stratified tremolite nephrite remain poorly constrained. To address this shortcoming, the mineralogy, geochemistry and Sr isotopic of host rock, altered marble, stratified tremolite nephrite and intrusive rock in the Dahua stratified tremolite nephrite deposit were studied. The results show: stratified tremolite nephrite mainly consists of aggregates of microcrystalline-cryptocrystalline tremolites with content exceeding 95%. The in situ rare earth elements (REEs) distribution pattern of hydrothermal calcite in the contact position between stratified tremolite nephrite and marble is similar to that of marine carbonate rock, showing obvious enrichment of HREE, which is different from calcite in limestone and marble. ⁸⁷Sr/⁸⁶Sr of stratified tremolite nephrite is relatively uniform, with an average value of 0.7070, within the range of Permian seawater. The mean value of Y/Ho in the hydrothermal calcite is 51.24, indicating that the marine fluid has not been impregnated by terrigenous materials. In summary, the hydrothermal fluid rich in Ca and Si is formed after marine carbonate rocks are altered by marine fluids. Hydrothermal fluids alter diabase rocks formed by altered minerals like titanite, chamosite, zoisite, etc. This process leads to the formation of metallogenic hydrothermal fluids abundant in Si, Ca, Fe and Mg. The metallogenic hydrothermal fluids migrate in faults and fractures of marble and crystallize to form tremolite nephrite under suitable ore-forming conditions. Full article

The mineralogical, fluid inclusion, and stable isotope (C, O) study was conducted on a Late Variscan Zn-Pb vein Bt23C, Příbram uranium and base-metal district, Bohemian Massif, Czech Republic. The vein is hosted by folded Proterozoic clastic sediments in exo-contact of a Devonian-to-Lower-Carboniferous granitic pluton. Siderite, dolomite-ankerite, calcite, quartz, baryte, galena, sphalerite, V-rich mica (roscoelite to an unnamed V-analogue of illite), and chlorite (chamosite) form the studied vein samples. The banded texture of the vein was modified by the episodic dissolution of earlier carbonates and/or sphalerite. Petrographic, microthermometric, and Raman studies of fluid inclusions proved a complicated fluid evolution, related to the activity of aqueous fluids and to an episode involving an aqueous–carbonic fluid mixture. Homogenization temperatures of aqueous inclusions decreased from ~210 to ~50 °C during the evolution of the vein, and salinity varied significantly from pure water up to 27 wt.% NaCl eq. The aqueous–carbonic fluid inclusions hosted by late quartz show highly variable phase compositions caused by the entrapment of accidental mixtures of a carbonic and an aqueous phase. Carbonic fluid is dominated by CO₂ with minor CH₄ and N₂, and the associated aqueous solution has a medium salinity (6–14 wt.% NaCl eq.). The low calculated fluid δ¹⁸O values (−4.7 to +3.6‰ V-SMOW) suggest a predominance of surface waters during the crystallization of dolomite-ankerite and calcite, combined with a well-mixed source of carbon with δ¹³C values ranging between −8.2 and −10.5‰ V-PDB. The participation of three fluid endmembers is probable: (i) early high-temperature high-salinity Na>Ca-Cl fluids from an unspecified “deep” source; (ii) late low-salinity low-temperature waters, likely infiltrating from overlying Permian freshwater partly evaporated piedmont basins; (iii) late high-salinity chloridic solutions with both high and low Ca/Na ratios, which can represent externally derived marine brines, and/or local shield brines. The source of volatiles can be (i) in deep crust, (ii) from interactions of fluids with sedimentary wall rocks and/or (iii) in overlying Permian piedmont basins containing, in places, coal seams. The event dealing with heterogeneous CO₂-bearing fluids yielded constraints on pressure conditions of ore formation (100–270 bar) as well as on the clarification of some additional genetic aspects of the Příbram’s ores, including the reasons for the widespread dissolution of older vein fill, the possible re-cycling of some ore-forming components, pH changes, and occasionally observed carbon isotope shift due to CO₂ degassing. Full article

The late Paleocene–early Eocene warm greenhouse conditions, characterized by elevated pCO₂ levels in the atmosphere and a dramatic increase in sea surface temperature, prompted abundant authigenic glauconite formation within the shallow marine sediments worldwide by lowering the net sedimentation rate, increasing organic productivity and expanding the oxygen minimum zones to shallow oceans. The early Eocene marginal marine Cambay Shale Formation experienced episodes of marine inundation represented by limestone–green shale alternations. The shales host abundant authigenic light-green, dark-green, and brown pellets. A detailed characterization of the pellets of the Valia and Vastan lignite mines, integrating the sedimentological, petrographical, mineralogical, and mineral geochemical data, suggests two distinct varieties of Fe–silicate formation, viz. glauconite and chamosite. While the glauconitic green pellets are ubiquitous to Valia and Vastan mines, brown chamosite pellets are confined within the basal part of the green shale facies alternating with fossiliferous limestone in the Vastan mine. The glauconites of the Valia mine manifest a ‘nascent’ to ‘slightly evolved’ maturation stage of glauconitization, whereas the glauconites of the Vastan mine represent the ‘evolved’ type. The limestone–green shale alternation in the Valia mine is overlain by a ~4 m-thick spherulitic mudstone facies comprising monomineralic sideritic spherulites, reflecting a pure FeCO₃ composition. The glauconites in the Cambay Shale Formation transformed from kaolinite-rich clay pellets under dys-oxic depositional conditions. The increasing anoxicity within the microenvironment, possibly amplified by the rapid oxidation of continent-derived organic matter, facilitated chamosite formation instead of glauconite. The increased freshwater influx into the marginal marine depositional environment resulted in immature, K-poor glauconites of the Valia mine. The formation of siderite spherulites overlying the limestone–green shale alternation relates to the beginning of the regressive phase of sedimentation. Full article

The Sungun Cu-Mo porphyry deposit forms part of the Ahar–Arasbaran Magmatic Belt (AAMB). Its host Miocene porphyry stock is quartz monzonitic in composition and is cut by intermediate dykes that post-date mineralization. These dykes contain pyroxene and enclaves of ambiguous origin. Dykes of microdiorite are observed within quartz diorite dykes, whereas later diorite dykes contain three different kinds of enclaves (diorite, quartz diorite and hornfels) of sizes between 1 and 10 cm. Enclaves consist of plagioclase, hornblende and biotite, with accessory sphene, quartz and apatite. Chlorite compositions in microdiorite are within the chamosite range, whereas they are within the clinochlore range in diorite enclaves. Microprobe analyses of pyroxene indicate an augitic composition (Fs13.38-22.79Wo29.1-33.57En48.53-56.61), consistent with an igneous origin. Hornblende of the diorite enclaves formed at pressures ranging between 3 and 5.3 kilobars and temperatures between 714 and 731 °C. Average oxygen fugacity during rock formation is −14.75. Such high oxygen fugacities suggest that the diorite formed near the boundaries of a convergent margin. Amphibole compositions suggest that the diorite enclaves are sub-alkaline to mildly alkaline, consistent with reported whole-rock chemistry of the Sungun magmas. Pyroxenes were formed at pressures ranging between 11 and 15 kilobars (33–45 km) and temperatures between 1100 and 1400 °C. The amount of Fe³⁺ in clinopyroxene is also consistent with high oxygen fugacity within their environment of crystallization. Overall, these results have implications for our understanding of the origin of the Sungun Cu-Mo porphyry magmas and their mineral deposits in a lower-crustal setting. Full article

The mineral chemistry of illite/mica and chlorites, together with the evaluation of textural data of low-temperature metaclastic rocks, plays an important role in determining their origin and metamorphic grade. This study aimed to investigate the chemical properties of phyllosilicates in early Paleozoic metaclastic rocks in the Eastern Tauride Belt, Türkiye. The textural (electron microscopy) and chemical (mineral chemistry analysis) analyses were performed on the samples representing different grades of metamorphism. The illites/micas and chlorites are observed as detrital (chlorite–mica stacks) and neoformation origin. Trioctahedral chlorites (chamosite) exhibit different chemistry for detrital and neoformed origin as well as the metamorphic grade. Tetrahedral Al and octahedral Fe + Mg increase, whereas octahedral Al decreases together with the increasing grade of metamorphism. The detrital chlorites have higher tetrahedral Al and Fe contents than their neoformed counterparts. Chlorite geothermometry data (detrital: 241–≥350 °C; neoformed: 201–268 °C) are compatible with the texture and illite Kübler index data. Illite/white-mica compositions display muscovite and Na-K mica. Tetrahedral Al and interlayer K + Na contents of illites/micas increase with metamorphic grade. Na-K mica and paragonite are observed as replacement-type developments within the detrital CMS. The obtained data indicate that phyllosilicate chemistry can be used effectively for determining the geological evolution of low-grade metamorphic sequences. Full article

Concrete structures perform poorly when withstanding thermal shock events, usually requiring repair or replacement after one single instance. In certain industries (such as petrol, metallurgic and ceramics), these events are not only likely but frequent, which represents a considerable financial burden. One option to solve this issue would be to decrease the heating rate imposed onto the concrete material through the use of a protective surface layer. In this work, the suitability of dunite and microgabbro as protective materials is explored through X-ray diffraction, thermal dilation, optical microscopy, X-ray microtomography, thermo-gravimetric analysis and a compressive test. Further, the thermal dilation was used as an input to simulate a composite concrete-rock wall and the respective stresses caused by a thermal shock event. The dehydration of chrysotile in dunite and the decomposition of analcime, chamosite and pumpellyite in microgabbro were both favourable for the performance of the stones in the desired application. The thermal stability and deformation were found in the range of what can be applied directly on concrete; however, it was clear that pre-heating treatment results in a far more durable system in a cyclic thermal load situation. Full article

Late Permian coal deposits are widely distributed throughout southwestern China. This paper describes the petrological composition of the last coal seam in the Longmendong section of the Emeishan area during the latest Changhsingian (Permian) and records important information regarding the evolution of the mass extinction event that occurred at the end of the Permian. The results show that the dominant coal maceral group is vitrinite, followed by liptinite and inertinite macerals, and the coal minerals include quartz, chamosite and pyrite. The pyrofusinite and carbon microparticles occurrence modes could have been formed during wildfires in the adjacent areas. The β-tridymite occurrence modes and the high proportions and occurrence modes of magmatic quartz indicate that synchronous felsic volcanic activity occurred during the peat mire accumulation period. The chamosite and quartz occurrence modes suggest that they primarily precipitated from Fe-Mg-rich siliceous solutions that was derived from the weathering of nearby Emeishan basalt. The pyritic coal balls occurrence modes in the C1 coal seam are likely the result of coal-forming plants and Fe-Mg-rich siliceous solutions in neutral to weak alkaline conditions during late syngenetic stages or early epigenetic stages within paleomires. Full article

Highly atypical mineralization involving Pd-Pt, Au-Ag, REE, Y, Zr, U, Th, and Cl-F-enriched minerals is found in zones with base metal sulfides (BMS; ~5 vol.% to 20 vol.%) in the eastern portion of the Oktyabrsky deposit in the Norilsk complex (Russia). The overall variations in Mg# index, 100 Mg/(Mg + Fe²⁺ + Mn), in host-rock minerals are 79.8 → 74.1 in olivine, 77.7 → 65.3 in orthopyroxene, 79.9 → 9.2 in clinopyroxene, and An_79.0 → An_3.7. The span of clinopyroxene and plagioclase compositions reflects their protracted crystallization from early magmatic to late interstitial associations. The magnesian chromite (Mg# 43.9) trends towards Cr-bearing magnetite with progressive buildups in oxygen fugacity; ilmenite varies from early Mg-rich to late Mn-rich variants. The main BMS are chalcopyrite, pyrrhotite, troilite, and Co-bearing pentlandite, with less abundant cubanite (or isocubanite), rare bornite, Co-bearing pyrite, Cd-bearing sphalerite (or wurtzite), altaite, members of the galena-clausthalite series and nickeline. A full series of Au-Ag alloy compositions is found with minor hessite, acanthite and argentopentlandite. The uncommon assemblage includes monazite-(Ce), thorite-coffinite, thorianite, uraninite, zirconolite, baddeleyite, zircon, bastnäsite-(La), and an unnamed metamict Y-dominant zirconolite-related mineral. About 20 species of PGM (platinum group minerals) were analyzed, including Pd-Pt tellurides, bismuthotellurides, bismuthides and stannides, Pd antimonides and plumbides, a Pd-Ag telluride, a Pt arsenide, a Pd-Ni arsenide, and unnamed Pd stannide-arsenide, Pd germanide-arsenide and Pt-Cu arseno-oxysulfide. The atypical assemblages are associated with Cl-rich annite with up to 7.54 wt.% Cl, Cl-rich hastingsite with up 4.06 wt.% Cl, ferro-hornblende (2.53 wt.% Cl), chlorapatite (>6 wt.% Cl) and extensive solid solutions of chlorapatite, fluorapatite and hydroxylapatite, Cl-bearing members of the chlorite group (chamosite; up to 0.96 wt.% Cl), and a Cl-bearing serpentine (up to 0.79 wt.% Cl). A decoupling of Cl and F in the geochemically evolved system is evident. The complex assemblages formed late from Cl-enriched fluids under subsolidus conditions of crystallization following extensive magmatic differentiation in the ore-bearing sequences. Full article

This study reconstructs the depositional conditions of ironstones within the Chulym-Yenisey basin and assesses the iron source. The detrital minerals of the studied deposits include quartz and feldspar. The authigenic minerals are goethite, siderite, aragonite, dolomite, calcite, apatite, barite, and pyrite. The clay components include minerals of the chlorite group (possible chamosite), nontronite, kaolinite, illite, and beidellite. Local bacterial sulfate reduction led to the formation of pyrite framboids in siltstone layers. The subsequent diagenetic iron reduction promoted the formation of chamosite from siderite. The goethite precipitation occurred in an oxidic aqueous environment. The Cretaceous continental sediments of the Ilek and Kia Formations of the Chulym-Yenisei depression consist of fine- and medium-grained, cross-stratified, poorly sorted litho-feldspatho-quartzose sandstones of fluvial channel origin alternating with bluish-gray siltstones and ironstones of floodplain–lacustrine–bog origin. Thin layers of iron-bearing rocks within siltstones formed in meromictic waters. The changes in geochemical proxies demonstrate fluctuations of paleoenvironmental conditions within the Cretaceous sequence. Siltstones and sandstones formed under humid and arid conditions, respectively. The primary iron source for sediments of the Chulym-Yenisey depression was determined as volcanogenic and igneous rocks of the Altai-Sayan mountainous region. Full article

Sandstone pore-plugging is a serious problem that bothers acid in situ leaching (ISL) uranium deposit, but currently, the mechanism of pore-plugging has not attracted much attention. In this study, using X-ray fluorescence, scanning electron microscope, optical microscope, and X-ray diffraction, we present both macro- and micro-evidence of pore-plugging occurred during acid in situ mining of sandstone uranium deposit at Yili Basin, NW (northwest) China. Our study reveals that in comparison with normal sandstones, the plugged sandstones are yellow in color and have relatively high contents of Fe and chamosite. The plugging in studied samples is mainly caused by precipitation of Fe(OH)₃ at a pH of 2.0–4.0 for quantitative effect and by precipitation of gypsum (CaSO₄·2H₂O) as well. Alteration/dissolution of chamosite and to a lesser extent, Fe-bearing microcline and muscovite, may have contributed iron for Fe(OH)₃ precipitation. It is suggested that adjustment of injection pH < 2.0 throughout the leaching passage would be an effective way to avoid/minimize this type of sandstone pore-plugging. Full article

Hyperspectral reflectance has the potential to provide rapid and low-cost mineralogical and chemical information that can be used to vector in mineral systems. However, the spectral signature of white mica and chlorite, despite numerous studies, is not fully understood. In this study, we review the mineralogy and chemistry of different white mica and chlorite types and investigate what mineralogical and chemical changes are responsible for the apparent shifts in the shortwave infrared (SWIR) spectroscopic absorption features. We demonstrate that the spectral signature of white mica is more complex than previously documented and is influenced by the Tschermak substitution, as well as the sum of interlayer cations. We show that an increase in the interlayer deficiencies towards illite is associated with a change from steep to shallow slopes between the wavelength position of the 2200 nm feature (2200 W) and Mg, Al_(VI) and Si. These changes in slope imply that white micas with different elemental chemistry may be associated with the same 2200 W values and vice versa, contrary to traditional interpretation. We recommend that traditional interpretations should only be used in true white mica with sum interlayer cations (I) > 0.95. The spectral signature of trioctahedral chlorite (clinochlore, sheridanite, chamosite and ripidolite) record similar spectral relationships to those observed in previous studies. However, dioctahedral Al-rich chlorite (sudoite, cookeite and donbassite) has a different spectral response with Mg increasing with 2250 W, which is the opposite of traditional trioctahedral chlorite spectral interpretation. In addition, it was shown that dioctahedral chlorite has a 2200 W absorption feature that may introduce erroneous spectral interpretations of white mica and chlorite mixtures. Therefore, care should be used when interpreting the spectral signature of chlorite. We recommend that spectral studies should be complemented with electron microprobe analyses on a subset of at least 30 samples to identify the type of muscovite and chlorite. This will allow the sum I of white mica to be obtained, as well as estimate the slope of 2200 W absorption trends with Mg, Al_(vi), and Si. Preliminary probe data will allow more accurate spectral interpretations and allow the user to understand the limitations in their hyperspectral datasets. Full article

This paper reports the mineralogy and geochemistry of the Late Permian C1 Coal from Bole and Laibin mines in eastern Yunnan, Southwestern China (C1 Coal in Laibin mine is composed of three layers termed B1, B2, and B3). The coals are characterized by medium-high ash yields and very low sulfur contents. Compared with average values of trace element concentrations in hard coals worldwide, the Bole and Laibin coals are enriched in V, Co, Cu, Zn, and Se, which were mainly derived from the sediment-source region of the Kangdian Upland. Major minerals in the coal samples and roof and floor strata include quartz, interstratified berthierine/chamosite (B/C), as well as kaolinite, mixed layer illite/smectite, calcite, pyrite, and anatase. Unlike a pure chamosite, the 7 Å peak of interstratified B/C is sharp and narrow, while the 14 Å peak is broad and weak, or absent in some coal samples. Interstratified B/C was largely precipitated from low-temperature Fe-rich and Mg-rich hydrothermal fluids or, in some cases, is an alteration product of kaolinite. Secondary phases of quartz, calcite, pyrite, kaolinite, chalcopyrite, gypsum, and REE-phosphates in the coal samples are the dominant authigenic minerals formed at syngenetic and early diagenetic stages. Four intra-seam partings in C1 Coal, B1, and B3 layers are identified as tonsteins derived from felsic volcanic ashes. These tonsteins consist mainly of cryptocrystalline kaolinite with graupen and vermicular textures, and minor amounts of high-temperature quartz, zircon, apatite, monazite, and anatase. The floor of the C1 Coal in the Bole mine is a tuffaceous claystone and consists of altered high-Ti basalt volcaniclastics, characterized by high concentrations of Zr, Nb, V, Co, Cu, and Zn, low Al₂O₃/TiO₂ ratio (~4.62), high Ti/Y ratio (~900), enrichment of middle rare earth elements, and positive Eu anomalies. Full article

The mode of occurrence and origin of highly-enriched trace elements, especially Ge, in Wulantuga high-Ge coal deposit have been widely reported. In this study, coal samples and several coalified trunks embedded within the roof strata are collected, which provides a good opportunity to further confirm if Ge is mainly associated with organic matter. Minerals in coal samples are mainly quartz, kaolinite, montmorillonite, pyrite, and gypsum, along with trace albite, barite, chlorite, and Fe-oxide, while those in coalified trunk samples include melanterite, pyrite, and gypsum, with traces of chlorite and magnesiocopiapite. Germanium, As, W, Sb, Hg, Be, and Cs are enriched in coal samples, and these elements are also enriched in the coalified trunks and roof glutenite. The elevated contents of Ge, As, W, Sb, and Hg were almost exclusively derived from the influx of hydrothermal fluids as evidenced by the presence of pyrite veins and chamosite as well as enhanced elemental associations of Ge-W and As-Sb-Hg in the studied lignite samples. The coalified trunks in the study area should be taken into consideration due to the high contents of hazardous elements that cause potential environmental impacts during mining waste disposal and land reclamation. Full article

The aim of this research was to study the rare earth (REE) minerals in ooidal ironstone deposits of the West Siberian basin and the Turgai depression. Authigenic minerals (monazite and cerite) were described, and their main mineral form was identified as light rare earth element phosphate (LREE-phosphate) in this study. LREE-phosphate is included in ferruginous ooids, peloids, and oncoids and forms a consistent mineral association with Fe-hydroxides (goethite and its hydrated amorphous derivatives) and Fe-rich layered silicates (Fe-illite-smectite, chamosite, berthierine). The constancy of the mineral association in two deposits of different ages indicates a general mechanism behind the formation of these minerals. LREE-phosphates (authigenic monazite) are characterized by microscopic sizes (up to 24 μm), diverse morphology (mainly spherical or xenomorphic), and occupy spaces between the micro-cortex in ferruginous spheroids. This mineral can be found in other deposits of ooidal ironstone. According to its mineralogical and chemical characteristics, LREE-phosphate mainly belongs to the authigenic (nodular or “gray”) monazite. However, the incomplete (not 100%) correspondence of Kikuchi bands with the reference monazite does not allow its reliable identification. Based on its small size, chemical leaching or bacterial interaction is recommended to extract REE from ooidal ironstone while predicting the associated removal of phosphorus from iron ore due to its dominant phosphate mineral form. Ooidal ironstone should be considered a complex deposit and an unconventional natural type of REE ores as an example of the largest Bakchar and Lisakovsk deposits. Full article