Search Results (13)

The Dashigou deposit is one of the most representative carbonatite-type Mo-REE deposits in the East Qinling metallogenic belt of China, with a molybdenum resource of more than 180 kt and a rare earth resource of 37.8 kt. Recent exploration has revealed a considerable scale of uranium mineralization within this deposit. Therefore, this study conducted detailed mineralogical and EPMA U-Th-Pb chemical dating on the uranium mineralization in the Dashigou deposit. The results indicate that the U-ore body in the Dashigou deposit mainly consists in carbonatite veins, and principally as anhedral, mesh-like uraninite. The mineral assemblage is characterized by uraninite + rutile + bastnasite + parisite or brannerite. The uraninite displays geochemical compositions of high Y and Ce and low Si, Ti, and Mg. The EPMA U-Th-Pb chemical dating is 144 ± 3.1 Ma, representing the Yanshanian uranium mineralization age in the region. The newly discovered uranium mineralization age indicates that the deposit experienced a uranium remobilization event during the Cretaceous and was formed in an intracontinental orogenic and extensional environment post-collision orogeny. Full article

The Huayangchuan uranium deposit, located in the west of the Xiaoqinling belt on the southern margin of the North China Craton, is a large U–Nb–Pb deposit accompanied with rare–earth elements. The Huayangchuan uranium deposit, discovered in the 1950s, has long been known as a carbonatite–type uranium deposit. Recently, new geological work has found uranium mineralization in many granitic pegmatite veins in the Huayangchuan deposit and adjacent areas. Here, we report a systematic investigation of the petrography, whole–rock geochemistry, zircon U–Pb ages, and in situ Lu–Hf isotopic characteristics of newly discovered U–rich granitic pegmatite veins in the west of Huayangchuan deposit. The petrological results showed that the lithology of the samples is granite pegmatite. The U–Pb ages of zircon were 1826.3 ± 7.9 and 1829 ± 11 Ma. Microscopically, the paragenetic characteristics of zircon, betafite, and uraninite exist in the intergranular fissures of K–feldspar and quartz, reflecting metallogenic phenomena in the rock formation process. Almost all whole–rock samples were rich in SiO₂ (64.37−70.69 wt.%), total alkalis (K₂O + Na₂O = 8.50–10.30 wt.%), and Al₂O₃ (12.20–14.41 wt.%) but poor in TiO₂ (0.23–0.73 wt.%), MgO (0.38–0.90 wt.%), CaO (1.23–2.22 wt.%), P₂O₅ (0.14–0.83 wt.%), and MnO (0.04–0.57 wt.%). Additionally, they showed enrichment of LILEs (such as Rb, Ba, Th, U, and K), depletion of HFSEs (such as Ta, P, Ti, and Hf), and no alkaline dark minerals, and the characteristics are intraplate A₁–type granite. The A₁–type granite displayed low zircon ε_Hf(t) values (−19.42–−15.02) with zircon two–stage Hf model aged 3.10–2.76 Ga, indicating that the U–rich granitic pegmatite was derived predominantly from partial melting of the ancient continental crust (such as the early Taihua group formed in Archean–Neoarchean). Combined with the above results and regional geological data, the U–rich granitic pegmatite discovered in the Huayangchuan deposit was formed in a post–collisional regime after the Luliang movement in the late Paleoproterozoic. This study suggests that future uranium prospecting work in this area should focus on late Paleoproterozoic U–rich granitic pegmatites. Full article

Geological and radiometric studies of outcrops aided by extensive subsurface exploration through drill holes in an otherwise soil-covered terrain revealed the existence of low grades, medium tonnage, and metasomatite types of polymetallic uranium deposits at Rohil in India. Microscopic studies, electronprobe micro analyses, and geochemical analyses of samples from lodes indicate the polymetallic nature of mineralisation involving copper and molybdenum, in addition to uranium. Wide variations in the composition of fluid (S-, F-, P-, and O-rich) led to the formation of sulphides, fluorite, U-phosphosilicate, quartz, and magnetite, respectively, and are associated with uraninite. Litho-geochemical analyses from the Rohil deposit indicate multifarious metasomatic alterations associated with polymetallic mineralisation occurring in veins. The major mineralogical and metasomatic controls on rock compositions and the extent of material transfer processes that influenced the host rocks and mineralisati on are quantified by molar element ratio studies and alteration plots. General element ratio (GER) diagrams on chemical analyses of rock samples reveal albitisation and chloritisation as major and microclinisation, sericitisation, carbonatisation, and silicification as minor wall rock alterations associated with ore mineralisation. The alteration box plot between the chlorite–carbonate–pyrite index (CCPI) and the Ishikawa alteration index (AI) indicates the influence of hydrothermal activity and dominance of both albitisation and chloritisation. The ore zone is controlled by meso- and microstructures and the geometry of the soda- and potash-metasomatised zone around hydrothermal veins. This zone contains several anastomosing mineralised veins defined by a prominent joint that is set in quartzite that strikes subparallel to the axial surface of the F₂ isoclinal folds and the pervasive schistosity S₁ in the quartz–feldspar–biotite schist. Aventurisation of albite and microcline, established through electron probe micro analyses, can be considered as a pathfinder for uranium mineralisation. The close association of uranium and metallic sulphide mineralisation with microstructural, mineralogical (albitisation, chloritisation, and microclinisation), and geochemical variations can be applied as suitable exploration guides in a similar geological set-up worldwide. Full article

The intracratonic Paleoproterozoic Nonacho Basin, deposited on the western margin of the Rae craton, contains historic polymetallic (i.e., U, Cu, Fe, Pb, Zn, Ag) occurrences spatially associated with its unconformable contact with underlying crystalline basement rocks and regionally occurring faults. This study presents the paragenesis, mineral chemistry and geochemistry of uranium mineralized rocks and minerals of the MacInnis Lake sub-basin of the Nonacho Basin, to evaluate the style and relative timing of uranium mineralization. Mineralization is restricted to regionally occurring deformation zones, and post-dates widely spread and pervasive albitization and more local Ba-rich K-feldspar alteration of host rocks. Uranium mineralized rocks show elevated concentration of Cu, Ag and Au relative to variably altered host rocks. Microscopic and compositionally heterogeneous altered uraninite occurs (i) as overgrowths on partially dissolved Cu-sulphides with magnetite in chlorite ± quartz, calcite veins, and (ii) with minor uranophane in hematite-sericite-chlorite ± quartz breccia and stockwork. Both uraninite types are Th poor (<0.09 wt.% ThO₂) and variably rich in SO₄ (up to 2.26 wt.%), suggesting a low-temperature hydrothermal origin in a relatively oxidized environment. Rare-earth element (+Y) concentrations in type-i uraninite are high, up to 9.5 wt.% Σ(REE+Y)₂O₃ with Ce_N/Y_N values > 1, similar to REE compositions of uraninite in metasomatic iron and alkali-calcic systems (MIAC), including low-temperature hematite-type IOCG-deposits (e.g., Olympic Dam, Gawler Craton, Australia) and albitite-hosted uranium deposits (e.g., Southern Breccia, Great Bear Magmatic Zone, Canada, and Gunnar Deposit, Beaverlodge District, Canada). Both uraninite types are variably rich in Ba (up to 3 wt.% BaO), a geochemical marker for MIAC systems, provided by the dissolution of earlier secondary Ba-rich K-feldspar. Chemical U-Th-Pb dating yields resetting ages of <875 ± 35 Ma for type-ii uraninite-uranophane, younger than strike-slip movement along regional structures of the basin that are spatially associated with the uranium occurrences. We suggest that MacInnis Lake uranium occurrences formed from oxidized hydrothermal fluids along previously altered (albitized, potassically altered) regional-scale faults. Uranium minerals precipitated on earlier Fe-rich sulfides (chalcopyrite, bornite), which acted as a redox trap for mineralization, in low-temperature (~310–330 °C, based on Al-in-chlorite thermometry) breccias and stockwork zones, late in a metasomatic iron and alkali-calcic alteration system. Full article

Chlorite is one of the most important hydrothermal minerals in many hydrothermal uranium deposits worldwide and is commonly closely associated with the uranium mineralization. Trace elements in chlorite have been extensively applied to fingerprinting the hydrothermal fluid evolution and indicating the concealed ore bodies in porphyry Cu (-Au) deposits and skarn-related Pb-Zn deposits. However, this approach was rarely attempted on hydrothermal uranium deposits to date. Xiangshan uranium ore field, located in the southeast part of Gan-Hang Metallogenic (or Volcanic) Belt (GHMB), is the largest volcanic-related ore field in the whole country. In this study, the focus was placed on the petrographic characteristics and trace elements in hydrothermal chlorite from two typical deposits (Zoujiashan and Yunji) at Xiangshan. Four types of chlorites were identified, i.e., Chl1-Y and Chl2 from Yunji deposit, and Chl1-Z and Chl3 from Zoujiashan deposit. The pre-ore Chl1-Y and Chl1-Z are formed through replacing the original magmatic biotite. Chl2 and Chl3 occur as veinlets or disseminated, and are closely associated with early-ore U mineralization and main-ore U mineralization, respectively. All the four types of chlorites are typically trioctahedral chlorite. Vein-type/disseminated Chl2 and Chl3 in ore veins were precipitated directly from the hydrothermal fluids through dissolution-migration-precipitation mechanism, whereas the replacement-type chlorite was formed by the dissolution–crystallization mechanism. Empirical geothermometry indicates that the chlorite from Yunji and Zoujiashan were crystallized at 179~277 °C, indicating a mesothermal-epithermal precipitation environment. EPMA and LA-ICP-MS results show that the replacement-type chlorite has relatively consistent compositions at Yunji and Zoujiashan. Both Chl2 and Chl3 are enriched in U, Th but depleted in Mn and Ti. Compared with the Chl2 related to early-ore U mineralization, Chl3 that formed at main-ore stage has higher concentrations of Fe, U, Th, REEs, Mn and Ti, as well as higer Fe/(Fe + Mg) ratios. Such compositional differences between Chl2 and Chl3 are mainly attributed to the formation temperatures and fluid compositions/natures. Combined with petrology and chemical compositions of different types of chlorite, we propose that the presence of vein-type/disseminated chlorite with high U and Fe/(Fe + Mg) ratio but relatively low Mn, Ti and Pb contents can be regarded as an effective vector toward the most economic (high U grade) mineralized zone, whereas the occurrence of Chl2 is likely to indicate the subeconomic U mineralization and less potential exploration for uranium at depth. Full article

The Mianhuakeng deposit is the most representative granite-related hydrothermal vein-type uranium deposit in South China; however, the characteristics of the mineralization-forming fluid and metallogenic mechanism are still less constrained. To address the scientific problems above, we investigated the trace element chemistry and sulfur isotope compositions in syn-mineralization pyrite and pitchblende from the Mianhuakeng uranium deposit. The trace element chemistry shows that the mineralization in the Mianhuakeng deposit belongs to an intermediate-to-low temperature hydrothermal system, which is consistent with the homogenization temperature distribution of fluid inclusions. Redox-sensitive elements (such as Co and Se) in syn-mineralization pyrite suggest a reductive nature of the mineralization-forming fluids. The fractionation between light and heavy REE in pitchblende from the Mianhuakeng deposit is most similar to those from the Changjiang pluton. The pronounced negative Eu anomaly is coincident with mineralization-bearing granites. The δ³⁴S values of syn-mineralization pyrite range from −10.2 to −1.4‰, which is higher than those values of pyrite from granites near the studied area and lower than the δ³⁴S values of pyrite from diabase in the ore district. The REE signatures of pitchblende and sulfur isotope composition of syn-mineralization pyrite suggest that the major U source for the Mianhuakeng deposit is most likely the Changjiang pluton, probably accompanied by the incorporation of mantle-derived fluids. The circulations of CO₂-rich hydrothermal fluids leached uranium from granite source rocks, especially from the Changjiang pluton. The change of physicochemical conditions of the mineralization-forming fluid resulted in the deposition of the uranium minerals in favorable structural traps to form the hydrothermal vein-type Mianhuakeng uranium deposit. Full article

The evolution characteristics of hydrothermal activity and superimposed uranium mineralization in the Qianjiadian ore field in southwestern Songliao Basin are still controversial and lack direct evidence. In this comprehensive study, a detailed identification of dolerite and hydrothermally altered un-mineralized sandstone and sandstone-hosted ore in the Yaojia Formation have been performed through the use of scanning electron microscopy observation, electron probe, carbon-oxygen-sulfur isotope, and fluid inclusion analyses. The results show that the hydrothermal fluid derived from the intermediate-basic magma intrusion is a low-temperature reducing alkaline fluid and rich in CO₂, Si, Zr, Ti, Fe, Mg, Mn, and Ca, producing different types of altered mineral assemblages in the rocks, including carbonation, pyritization, sphalerite mineralization, clausthalite mineralization, silicification, and biotitization. Specifically, the carbonate minerals in sandstone are mixed products of deep hydrothermal fluid and meteoric water, with carbon and oxygen isotopes ranging from −5.2‰ to −1.7‰ and −20.4‰ to −11.1‰, respectively. Carbon source of the carbonate minerals in dolerite is mainly inorganic carbon produced at the late stage of intermediate-basic magma evolution, with carbon and oxygen isotopes from −16.1‰ to −7.2‰ and −18.2‰ to −14.5‰, respectively. Various carbonate minerals in the rocks may have been precipitated by the hydrothermal fluid after the magmatic stage, due to the change of its CO₂ fugacity, temperature, and cation concentration during the long-term evolution stage. A series of carbonate minerals were generated as calcite, dolomite, ankerite, ferromanganese dolomite, and dawsonite. The precipitation processes and different types of carbonate mineral mixtures identified in this study mainly occur as parallel, gradual transition, interlacing, or inclusion metasomatism in the same vein body, without obvious mineralogical and petrologic characteristics of penetrating relationship. Homogenization temperature of fluid inclusions in calcite is high, in the range of 203–234 °C, with a low salinity of 0.71–4.34% NaCl, and the data range is relatively concentrated. Homogenization temperature of fluid inclusions in ankerite is usually low, ranging from 100 °C to 232 °C, with a high salinity of 4.18–9.98% NaCl. The precipitation processes of carbonate minerals and the results of this study are basically in consistent. Overall, the sandstone-type uranium deposits have a temporal and genetic relationship with hydrothermal activities during Paleogene. (1) Hydrothermal activity was directly involved in uranium mineralization, result in dissolution and reprecipitation of earlier uranium minerals, forming uranium-bearing ankerite and complexes containing uranium, zirconium, silicon, and titanium. (2) Hydrothermal fluid activity provided reducing agent to promote hydrocarbon generation from pyrolysis of carbonaceous fragments and accelerate uranium precipitation rate. (3) Regional water stagnation prolongs reaction time, contributing to huge uranium enrichment. This study provides new petrologic, mineralogical, and geochemical evidence for multi-fluid coupled and superimposed mineralization of sandstone-hosted uranium deposits in the sedimentary basin. Full article

The middle Anisian extensional tectonics of the Neotethyan realm developed a small, isolated carbonate platform in the middle part of the Balaton Highland (western Hungary), resulted in the deposition of uranium-bearing seamount phosphorite on the top of the drowned platform and produced some epigenetic fluorite veins in the Middle Triassic sequence. The stable C-O isotope data of carbonates are shifted from the typical Triassic carbonate ranges, confirming the epigenetic-hydrothermal origin of veining. Primary fluid inclusions in fluorite indicate that these veins were formed from low temperature (85–169 °C) and high salinity NaCl + CaCl₂ + H₂O type (apparent total salinity: 15.91–22.46 NaCl wt%) hydrothermal fluids, similar to parent fluids of the Alpine-type Pb-Zn deposits. These findings indicate that the Triassic regional fluid circulation systems in the Alpine platform carbonates also affected the area of the Balaton Highland. This is also in agreement with the previously established palinspatic tectonic reconstructions indicating that the Triassic carbonate and basement units in the Balaton Highland area were a part of the Southern Alpine. Similar fluorite veining in phosphorite deposits is also known in the Southern Alpine areas (e.g., Monte San Giorgi, Italy). Raman spectroscopic analyses detected H₂ gas in the vapor phase of the fluid inclusions and a defect-rich fluorite structure in violet to black colored growth zones. This unique phenomenon is assumed to be the result of interaction between the uranium-rich phosphorite and the parent fluids of the epigenetic fluorite veins. Full article

Granite-related uranium ore is an important uranium resource type in China and worldwide. Whether the uranium geochemical theory “U⁶⁺ oxidative migration and U⁴⁺ reductive precipitation” is applicable to the granite-related uranium mineralization theory has not been determined. Detailed field and petrographic work, as well as scanning electron microscopy energy spectrum analysis, are conducted in this study to analyze the relationship between uranium minerals and pyrite from different ore types and evaluate the mechanism for the precipitation and enrichment of uranium in the Mianhuakeng uranium deposit of northern Guangdong. Uranium ore bodies in the Mianhuakeng deposit generally occur as vein-filling or vein-disseminated types. Four different kinds of ores are recognized: fluorite, carbonate, siliceous, and reddening types. Despite differences in the mineral assemblages, veined ores share similar characteristics and show that uranium minerals (1) occur in the central part or periphery of vein-filling ores or in interphase arrangements with syn-ore fluorite, quartz, or calcite veins; (2) occur as veinlets or are disseminated in cataclastic altered granite; (3) are inlaid with gangue minerals, primarily calcite, fluorite, and microcrystalline quartz; and (4) are closely associated with pyrite in aggregates or relatively independent states, forming straight boundaries with syn-ore gangue minerals that have euhedral and intact crystals and show mosaic growth features. All these results indicate that both pyrite and uranium minerals are co-crystallized products of the ore-forming fluid. Combined with previous research suggesting that the reducing fluid was sourced from mantle, this study shows that decreased pressure and temperature, as well as changes in pH and the solubility (saturation) of changes, rather than the redox reaction, caused the uranium precipitation in the Mianhuakeng deposit. Full article

The Huangsha uranium mining area is located in the Qingzhangshan uranium-bearing complex granite of the Middle Nanling Range, Southeast China. This uranium mining area contains three uranium deposits (Liangsanzhai, Egongtang, and Shangjiao) and multiple uranium occurrences, showing favorable mineralization conditions and prospecting potential for uranium mineral resources. Chloritization is one of the most important alteration types and prospecting indicators in this mining area. This study aims to unravel the formation environment of chlorites and the relationship between chloritization and uranium mineralization, based on detailed field work and petrographic studies of the wallrock and ore samples from the Huangsha uranium mining area. An electron probe microanalyzer (EPMA) was used in this study to analyze the paragenetic association, morphology, and chemical compositions of chlorite, to classify chemical types and to calculate formation temperatures and n(Al)/n(Al + Mg + Fe) values of chlorite. The formation mechanism and the relationship with uranium mineralization of the uranium mining area are presented. Some conclusions from this study are: (1) There are five types of chlorites, including the chlorite formed by the alteration of biotite (type-I), by the metasomatism of feldspar with Fe–Mg hydrothermal fluids (type-II), chlorite vein/veinlet filling in fissures (type-III), chlorite closely associated with uranium minerals (type-IV), and chlorite transformed from clay minerals by adsorbing Mg- and Fe-components (type-V). (2) The chlorite in the Huangsha uranium mining area belongs to iron-rich chlorite and is mainly composed of chamosite, partly clinochlore, which are the products of multiple stages of hydrothermal action. The original rocks are derived from argillite, and their formation temperatures vary from 195.7 °C to 283.0 °C, with an average of 233.2 °C, suggesting they formed under a medium to low temperature conditions. (3) The chlorites were formed under reducing conditions with low oxygen fugacity and relatively high sulfur fugacity through two formation mechanisms: dissolution–precipitation and dissolution–migration–precipitation; (4) The chloritization provided the required environment for uranium mineralization, and promoted the activation, migration, and deposition of uranium. Full article

Uraninite-coffinite vein-type mineralisation with significant predominance of uraninite over coffinite occurs in the Příbram, Jáchymov and Horní Slavkov ore districts and the Potůčky, Zálesí and Předbořice uranium deposits. These uranium deposits are hosted by faults that are mostly developed in low- to high-grade metamorphic rocks of the basement of the Bohemian Massif. Textural features and the chemical composition of uraninite, coffinite and ningyoite were studied using an electron microprobe. Collomorphic uraninite was the only primary uranium mineral in all deposits studied. The uraninites contained variable and elevated concentrations of PbO (1.5 wt %–5.4 wt %), CaO (0.7 wt %–8.3 wt %), and SiO₂ (up to 10.0 wt %), whereas the contents of Th, Zr, REE and Y were usually below the detection limits of the electron microprobe. Coffinite usually forms by gradual coffinitization of uraninite in ore deposits and the concentration of CaO was lower than that in uraninites, varying from 0.6 wt % to 6.5 wt %. Coffinite from the Jáchymov ore district was partly enriched in Zr (up to 3.3 wt % ZrO₂) and Y (up to 5.5 wt % Y₂O₃), and from the Potůčky uranium deposit, was distinctly enriched in P (up to 8.8 wt % P₂O₅), occurring in association with ningyoite. The chemical composition of ningyoite was similar to that from type locality; however, ningyoite from Potůčky was distinctly enriched in REE, containing up to 22.3 wt % REE₂O₃. Full article

New geological, bulk chemical and mineralogical (QEMSCAN and FEG-EPMA) data are presented for albitite-type uranium deposits of the Mount Isa region of Queensland, Australia. Early albitisation of interbedded metabasalt and metasiltstone predated intense deformation along D₂ high strain (mylonite) zones. The early sodic alteration paragenetic stage includes albite, riebeckite, aegirine, apatite, zircon and magnetite. This paragenetic stage was overprinted by potassic microveins, containing K-feldspar, biotite, coffinite, brannerite, rare uraninite, ilmenite and rutile. An unusual U-Zr phase has also been identified which exhibits continuous solid solution with a uranium silicate possibly coffinite or nenadkevite. Calcite, epidote and sulphide veinlets represent the latest stage of mineralisation. This transition from ductile deformation and sodic alteration to vein-controlled uranium is mirrored in other examples of the deposit type. The association of uranium with F-rich minerals and a suite of high field strength elements; phosphorous and zirconium is interpreted to be indicative of a magmatic rather than metamorphic or basinal fluid source. No large intrusions of appropriate age outcrop near the deposits; but we suggest a relationship with B- and Be-rich pegmatites and quartz-tourmaline veins. Full article

Albitite-type uranium deposits are widely distributed, usually of low grade (<1% U₃O₈), but are often large and collectively contain over 1 million tonnes of U₃O₈. Uranium is hosted in a wide range of metamorphic lithologies, whose only common characteristic is that they have been extensively mylonitised. Ore minerals are disseminated and rarely in megascopic veins, within and adjacent to albitised mylonites. Grain size is uniformly fine, generally less than 50 microns. Scanning electron microscopy reveals that spatial association between uranium and various Ti-bearing phases is common. Gangue minerals include albite, carbonates (calcite and dolomite), and sodic pyroxene and amphibole. The ore rarely contains economic metals apart from uranium, phosphorous at Itataia being an exception. There is widespread evidence of hydrothermal zirconium mobility and hydrothermal zircon and other Zr phases are frequent and in some cases abundant gangue minerals. Positive correlations are noted between uranium and various high field strength elements. The group remains poorly described and understood, but a link to iron-oxide copper-gold (IOCG) deposits and/or carbonatite and/or alkaline magmatism is plausible. Full article