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[Display omitted] • Ore-forming materials were sourced from the Niutitang Formation and deep crust. • Ore-forming fluids were derived from meteoric water. • Redox and fluid-rock reaction caused ore precipitation. • Tectonic system and overprinting zone of black-red alterations are indicators for prospecting. The Baimadong uranium deposit is situated in the Yangtze Craton, SW China, and is one of the most representative carbonate-hosted uranium deposits in China. Uranium mineralization has spatial and genetical relationships with black and red alterations that has been documented by previous studies. However, the signature, source, and evaluation of ore-forming fluids producing the alterations and mineralization remain poorly understood. Fluid inclusions hosted in different generations of hydrothermal calcite have been analyzed in this study, including Cal 1 (pre-ore stage), Cal 2 (early ore stage), and Cal 3 (main ore stage). Three types of fluid inclusions were identified: liquid-dominated biphase, vapor-dominated biphase, and vapor-only monophase. Based on fluid inclusion microthermometry using the FIA method, the fluids associated with Cal 2 are characterized by relatively higher temperature (∼243 ℃) and salinity (5.3 wt% NaCl equiv.) compared with fluids associated with Cal 1 (T h = ∼221 ℃; Salinity = 1.9 wt% NaCl equiv.) and Cal 3 (T h = ∼144 ℃; Salinity = 2.5 wt% NaCl equiv.). The results of stable isotopes (C, O, and S) indicate that the carbon in pre-ore stage fluids was dominantly originated from host marine carbonate rocks (δ13C fluid-PDB = −3.0 to 0.5 ‰; δ18O fluid-SMOW = 4.8 to 11.3 ‰), the carbon and sulfur in early ore-forming fluids were mainly derived from the Niutitang Formation with minor from deep crust (δ13C fluid-PDB = −11.2 to −8.4 ‰; δ18O fluid-SMOW = 7.9 to 11.4 ‰; δ34S v-CDT = −11.3 to + 2.1 ‰), whereas the main ore-forming fluids were sourced from meteoric fluids (δ13C fluid-PDB = −8.6 to −4.9 ‰; δ18O fluid-SMOW = 0.4 to 8.6 ‰). These results reveal that redox reaction as well as fluid-rock reaction are key factors controlling the large-scale uranium mineralization at Baimadong. Combined with these observations, geological setting, and previous geochemical features, we suggest that tectonic system together with overprinting zone of black and red alterations are indicators for exploration of carbonate-hosted uranium deposit in South China and elsewhere worldwide. [ABSTRACT FROM AUTHOR]

Megacrystalline uraninite (up to one centimeter in size) represents one of the most important discoveries in uranium mineralogy in the western margin of the Yangtze Block and even in China in recent years. However, the genesis of megacrystalline uraninite remains controversial. In this study, the megacrystalline uraninite found in the felsic and quartz veins in the Haita area is examined for the first time. The study examined the geochemical characteristics of uraninite in the two veins and resulted in two primary findings. (1) The genesis of the uraninite was likely intrusive and was closely related to partial melting. (2) The quartz vein and feldspar vein are cogenetic and have a simple differentiation evolution relationship. Therefore, the partial melting of felsic materials during migmatization may be the most important mechanism of uranium mineralization in the study area. Furthermore, further simple fractional crystallization may be another important mechanism for the formation of megacrystalline uraninite. This study enriches the REE database of uraninite in uranium deposits worldwide, which is meaningful for studying the genesis of megacrystalline uraninite. [ABSTRACT FROM AUTHOR]

The Datian uranium deposit is a migmatite-hosted, high temperature, hydrothermal deposit in the Kangdian region. Detailed information on the chemical composition and formation age of the uraninite remains lacking, which impedes our understanding of uraninite genesis. Two phases of uraninite have been identified according to their relationships with other minerals and their field relationships. The phase 1 (Ur1) uraninite is characterized by local development of microfractures and pores in the crystal of uraninite, a scattered distribution, and irregular crystal shapes, and it is associated with ilmenite, biotite, and rare earth element (REE) minerals (monazite and xenotime). The phase 2 uraninite (Ur2) has anhedral crystal shapes with well-developed microfractures and pores and is associated with pyrite, albite, pyrrhotite, molybdenite, zircon, and chlorite. X-ray element mapping revealed that the distributions of U, Th, and Pb in the Ur1 uraninite are homogeneous, whereas those in the Ur2 uraninite are heterogeneous. The results of the electron microprobe analysis (EMPA) show that the UO2 and PbO contents of the Ur1 and Ur2 uraninite do not vary significantly. The high ThO2 contents of the Ur1 (1.08–1.68 wt %) and Ur2 uraninite (3.41–4.83 wt %) indicate that they formed at different temperatures. The laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS) analysis results show that the ∑REE of the Ur1 uraninite (3747.5–7032.3 ppm) is lower than that of the Ur2 uraninite (8369.2–11,484.3 ppm), and the REE patterns of the Ur1 and Ur2 uraninite are sickle-shaped with large negative Eu anomalies. The LA-ICP-MS U–Pb dating results revealed that the ages of the Ur1 (841.4 ± 4.0 Ma) and Ur2 (834.5 ± 4.1 Ma–837.2 ± 4.5 Ma) uraninite are in consistent with that of the migmatite. Thus, the Datian uranium deposit underwent at least two hydrothermal events, and the uraninite was formed due to the migmatization. [ABSTRACT FROM AUTHOR]

The article presents a study which discusses metallogenic regularity of hydrothermal uranium deposits in the migmatite of the Kangdian Axis. It mentions that the uranium mineralization is found in the iron oxide copper gold deposit. It also reveals that spatial distribution of uranium mineralization is controlled by migmatite that related to ductile shear zones.

• Baimadong U deposit is hosted by carbonate rocks and is associated with black and red alterations. • Black alteration is characterized by exogenous graphite and bitumen. • Red alteration is marked by precipitation of hematite and goethite. • Black alteration provides reducing agents for, and red alteration results from, U mineralization. The Baimadong uranium deposit is hosted in carbonate rocks that were subjected to extensive black and red alterations, silicification and argillization, and is assigned to the carbonaceous-siliceous-pelitic rock-type uranium deposits in the Chinese literature. However, the nature of the mineralization, especially the black and red alterations and their relationship with uranium mineralization, remains poorly understood. Petrographic and Raman spectroscopic studies indicate that the black material are organic matter mainly composed of graphite and bitumen, whereas the red-altered rocks are characterized by abundant iron oxides. Crosscutting relationships suggest that the black alteration occurred before the red alteration. Comparison of whole-rock geochemistry between the different types of rocks suggests that total organic carbon (TOC), U and total organic sulfur (TOS) were gained through the black alteration, and FeOT was gained through the red alteration, whereas total inorganic carbon (TIC), CaO and MgO were lost in both types of alterations. The δ13C org (PDB) values and biomarker characteristics of the black-altered rocks suggest that the organic matter was derived from the black shale of the Niutitang Formation underneath the deposit. U enrichment is associated with both the black and red alterations, and shows positive correlations with Al 2 O 3 , K 2 O, TiO 2 , SiO 2 , TOC and TOS. It is proposed that the uranium mineralization at Baimadong resulted from superposition of two fluid events controlled by a common structural system. First, petroleum generated in the black shales of the Niutitang Formation and hydrothermal fluids migrated along cross-formational faults to the carbonate rocks of the Qingxudong and Shilengshui formations, causing the black alteration and preliminary uranium enrichment. Second, an oxidizing, U-bearing fluid flowed through the same structure and precipitated uraninite through reaction with the black-altered rocks, accompanied by precipitation of hematite and goethite as marked by the red alteration. The combination of black and red alterations with major faults may be used as a mineralization indicator in the exploration of this type of U deposits. [ABSTRACT FROM AUTHOR]

[Display omitted] • Co-existing pyrite and calcite with uranium minerals play a significant role in ISL of uranium. • Gypsum produced by pyrite and calcite in CO 2 + O 2 environment disadvantages the leaching of uranium. • Secondary hexavalent uranium minerals will be produced in the ore layer of a neutral environment. Oxidative weathering of pyrite, a widespread iron sulfide mineral, is crucial for the uranium mineralization in sandstone-hosted uranium deposits and the ore utilization leaching under manual intervention. To understand the behavior of pyrite under CO 2 + O 2 leaching conditions in sandstone-hosted uranium deposits, samples of uranium ore from the mineralized zone of the Qianjiadian IV uranium deposit located in the lower section of the Yaojia Formation were collected for this study. The stirring leaching experiment was carried out through the processes of the pyrite-bearing uranium ore samples thinned before and after the reaction, followed by an optical microscopic study and the TESCAN Integrated Mineral Analyzer analysis, and finally, the thermodynamic simulation by making use of PHREEQC3.0. The results revealed the following: (1) The dissolution particles of pyrite become smaller, which may increase the porosity of the ore layer and the exposure ratio of uranium minerals. And more soluble pyrite with a high free surface will be more competitive with uranium minerals for the consumption of O 2. (2) The ion (Fe2+) produced by the dissolution of pyrite will be oxidized to Fe3+ by excess O 2 (4 mol), which provides an oxidant for the oxidation of uranium minerals, and the generated SO 4 2- will combine with the Ca2+ released from calcite to form a permanent precipitate of gypsum, which may block pores and cover the uranium ore. (3) Pyrite and calcite will consume O 2 and CO 2 in the injection system, thus jointly inhibiting the leaching of uranium minerals. After the injection of excessive CO 2 and O 2 , the concentration of Ca2+, SO 4 2-, Fe3+, UO 2 2+, and HCO 3 – in the system will continue to accumulate, resulting in the secondary precipitation of calcite, co-precipitation of gypsum, iron minerals, colloids, and hexavalent uranium minerals, resulting in plugging pores and seriously affecting the effective leaching of uranium. This study contributes to the understanding of the behavior of pyrite during uranium recovery through CO 2 + O 2 leaching. It also contributes to the understanding of quantitative uranium mineralization in sandstone-hosted uranium deposits and process parameters in in-situ leaching (ISL) of uranium. [ABSTRACT FROM AUTHOR]

• Clay minerals and carbonate cementation are associated with U mineralization. • δD and δ18O values of clay minerals suggesting meteoric origin of the ore fluid. • Hydrocarbons may have played an important role in U mineralization. • H-O-C isotopes suggest a transient interface between oxidizing/reducing fluids. The Meso-Cenozoic Yili Basin in northwestern China hosts important uranium and coal resources. The uranium deposits are mainly hosted by sandstones and are characterized by clay and carbonate alterations within and surrounding the orebodies. H-O-C isotopes of clay minerals and carbonate cement in the different alteration zones of the uranium deposits in the southern margin of the Yili Basin are summarized to examine the mechanisms of uranium mineralization. The alteration zones associated with the uranium mineralization include an intensely oxidized zone, a weakly oxidized zone, a transitional (mineralization) zone, and a reduced zone. The δD and δ18O values of the parent fluids calculated from clay minerals from the different alteration zones show a linear trend that intersects the global meteoric line at a point with a δ18O V-SMOW of ca. −5‰ and a δD V-SMOW of ca. −30‰, which coincide with the upper end of the δD – δ18O trend (along the meteoric line) of formation waters in the basin, suggesting that the uranium mineralizing fluid was of meteoric origin. The general trends of decreasing δD and δ13C and increasing δ18O from the intensely oxidized zone to the reduced zone, together with the fact that calculated δD V-SMOW values of the mineralizing fluids are lower than the original meteoric fluid, and that the δ13C values of the calcite cement overlap with those of organic matter in sedimentary rocks, suggest that hydrocarbons were involved in uranium mineralization. The hydrocarbons may have been important reducing agents causing precipitation of uranium minerals. The hydrogen ion released from oxidation of the hydrocarbons may have been buffered by the formation of clay minerals, which favors co-development of clay alteration and calcite cement. Deviation of H-O-C isotopes from the general variation trends as expected from the above redox mechanism likely resulted from the dynamic nature of the redox front, which changed its position in response to hydrodynamic balance between a downward flow of uranium-bearing, oxidizing fluid and an upward flow of reductants-bearing, reducing fluid from the lower part of the basin. [ABSTRACT FROM AUTHOR]