The Guangshigou deposit is the largest pegmatite-type uranium deposit in the Shangdan domain of the North Qinling Orogenic Belt, which is characterized by the enrichment of uraninite hosted in biotite granitic pegmatites. At Guangshigou, uraninite commonly occurs as mineral inclusions in quartz, K-feldspar and biotite or in interstices of these rock-forming minerals with magmatic characteristics (e.g., U/Th < 100, high ThO₂, Y₂O₃ and REE₂O₃ contents and low concentrations of CaO, FeO and SiO₂). It crystallized at 407.6 ± 2.9 Ma from fractionated calc-alkaline high-K pegmatitic melts under conditions of 470–700 °C and 2.4–3.4 kbar as deduced by the compositions of coexisting peritectic biotite. The primary uranium mineralization took place during the Late Caledonian post-collisional extension in the North Qinling Orogen. After this magmatic event, uraninite has experienced multiple episodes of fluid-assisted metasomatism, which generated an alteration halo of mineral assemblages. The alteration halo (or radiohalo) was the result of the combined effects of metamictization and metasomatism characterized by an assemblage of goethite, coffinite and an unidentified aluminosilicate (probably clay minerals) around altered uraninite. This fluid-assisted alteration was concomitant with the albitization of K-feldspar subsequently followed by the coffinitization of uraninite during the major period of 84.9–143.6 Ma, as determined by U-Th-Pb chemical ages. Further investigations revealed that the metasomatic overprinting on uraninite initially and preferentially took place along microcracks or cavities induced by metamictization and promoted their amorphization, followed by the release of U and Pb from structure and the incorporation of K, Ca and Si from the fluids, finally resulting in various degrees of uraninite coffinitization. The released U and Pb were transported by alkali-rich, relatively oxidizing fluids and then re-precipitated locally as coffinite and an amorphous U-Pb-rich silicate under low to moderate temperature conditions (85–174 °C). The compositional changes in primary uraninite, its structure amorphization together with the paragenetic sequence of secondary phases, therefore, corroborate a combined result of intense metamictization of uraninite and an influx of alkali–metasomatic fluids during the Late Mesozoic Yanshanian magmatic event in the region. Hence, the remobilization and circulation of uranium in the North Qinling Orogen was most likely driven by post-Caledonian magmatism and hydrothermal activities related to large-scale tectonic events. In this regards, Paleozoic pegmatite-type uranium mineralization may represent a significant uranium source for Mesozoic hydrothermal mineralization identified in the Qinling Orogenic Belt.

Pegmatite-type uranium mineralization occurs in the Shangdan domain of the North Qinling Orogenic Belt, representing a significant uraniferous province. The Guangshigou deposit is the largest U deposit of the district. Within the North Qinling area, a series of Caledonian granitic igneous rocks intruded the Proterozoic metamorphic rocks of the Qinling Group in two magmatic stages: (i) the Early Silurian Huichizi granite that was derived from a low degree of partial melting of thickened lower basaltic crust combined with mantle-derived materials following the subduction of the Shangdan Ocean; and (ii) the Late Silurian–Early Devonian Damaogou granite and associated pegmatites derived from the same source but emplaced in a late tectonic post-collisional extension environment. In the Guangshigou deposit, the U mineralization mainly occurs as uraninite disseminated in U-rich granitic biotite pegmatites, which formed by assimilation-fractional crystallization magmatic processes. Petrographic observations showed evidence for coeval crystallization of uraninite and other rock-forming minerals of the host pegmatite including quartz, feldspar, biotite, zircon, monazite, apatite, and xenotime. In addition, the low U/Th ratios (~19) and Th, REE, and Y enrichments characterized a magmatic origin for uraninite, which was likely derived from fractionated high-K calc-alkaline pegmatitic magma that experienced various degrees of crustal material contamination. In situ U-Pb isotopic dating performed by Secondary-Ion Mass Spectrometry (SIMS) on uraninite from the Guangshigou deposit yielded a crystallization age of 412 ± 3 Ma, which is concomitant (within errors) with the emplacement age of the host pegmatite (415 ± 2 Ma) and constrained the U ore genesis to the Early Devonian, which corresponds to the late Caledonian post-collisional extension in the North Qinling area. Uraninite then experienced various degrees of metamictization and/or post-Caledonian hydrothermal alteration characterized by an alteration rim associated with coffinite, chlorite and limonite. Finally, the characteristics of the pegmatite-related Guangshigou deposit exhibiting Th-rich uraninite which was the product of assimilation-fractional crystallization of pegmatitic magma defined a model significantly different than the one established for the world-class Rössing deposit characterized by Th-poor uraninite hosted in alaskite dykes formed by low degree of partial melting of U-rich metasediments.

The Shiquanhe–Laguoco–Yongzhu–Jiali ophiolite mélange belt in Tibet includes the Laguoco Tso ophiolite as part of its western segment. Researchers studying the evolution of the Tibetan Plateau and the Tethys have taken a keen interest in the debated relationship between this ophiolite belt and the Bangong–Nujiang ophiolite belt. However, there is little research in this field. This study reports the rock geochemistry, SIMS (the secondary ion mass spectrometry) zircon U-Pb ages, and O isotope compositions of gabbro from the Laguoco ophiolite. Gabbro has substantial depletion in HFSEs (the high field strength elements) such as Th, Nb, Zr, and Hf, as well as exhibits comparatively high Mg^# (80.6 on average), and low K, N, P, and Ti contents. Therefore, it was possibly formed in an intra oceanic subduction island arc environment originating from ~30% partial melting of the depleted spinel lherzolite. The SIMS zircon U-Pb ages of the gabbro samples are 187 ± 1.2 Ma and 189 ± 2.1 Ma, and the weighted averages of δ¹⁸O are 5.24‰ ± 0.12‰ and 5.34‰ ± 0.13‰, which are close to mantle-derived zircon δ¹⁸O (5.3‰ ± 0.3‰). These results suggest that during the Early Jurassic, the Laguoco ophiolite recorded the intra oceanic subduction of the northern branch of the Neo-Tethys.

The Qianjiadian uranium deposit is a typical interstratified oxidized zone sandstone-hosted uranium deposit hosted in the Upper Cretaceous Yaojia Formation of the southern Songliao Basin. Despite its significance, little research has been conducted on the relationship between trace elements, REEs, and uranium mineralization in this deposit. This study presents new geochemical data from sandstones in the oxidation, transition, and reduction zones. The sandstones in the transition zone are highly enriched in U and moderately enriched in Mo, Cd, and V compared to those in the oxidation and reduction zones. They are also weakly enriched in Co, Ni, and Zn. The oxidation and transition zone sandstones have higher ∑LREE and ∑HREE contents than those in the reduction zone. However, the oxidation zone sandstones are characterized by LREE enrichment and flat HRRE distribution, while the transition zone sandstones show HRRE enrichment and flat LREE distribution. These trace element and REE differentiation characteristics within each subzone are closely related to the geological process of interstratified oxygenation. Oxygenated uranium-bearing fluids from southwestern provenance areas carried multiple trace elements and REEs and infiltrated along the oxidation sandstones to reach the Yaojia Formation’s transition zone. During this process, a certain amount of Mo, V, Cd, and LREE from the oxygenated ore-forming fluids was precipitated by Fe-Mn hydroxide adsorption or calcite and siderite cementation. Meanwhile, about 20.33% of preexisting U in the oxidation zone sandstones was continuously extracted and entered into the oxygenated ore-forming fluids. In the transition zone, where dissolved oxygen was exhausted and hydrocarbons were continuously injected, U, Mo, Cd, V, Co, Ni, Zn, and REEs were unloaded and precipitated as uranium minerals, sulfide minerals, or carbonate minerals. The enrichment of Mo, Cd, V, and HREEs in the sandstones can serve as new prospecting indicators for the Qianjiadian uranium deposit.