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 new mineral, gysinite-(La), with the ideal formula PbLa(CO₃)₂(OH)⋅H₂O, has been discovered in lujavrite from the Saima alkaline complex, Liaoning Province, China. It commonly occurs as subhedral to anhedral, granular and platy crystals of 5 to 50 μm in size, in interstices or enclosed in microcline, aegirine and nepheline. Associated minerals include nepheline, aegirine, microcline, natrolite, eudialyte, lamprophyllite, bastnäsite-(Ce), parasite-(Ce), ancylite-(La), ancylite-(Ce), bobtraillite, britholite-(Ce), thorite, calcite and galena. The crystallisation of gysinite-(La) may be related to the post-magmatic carbonation event. Gysinite-(La) crystals are generally transparent, colourless, or pale yellow, with a vitreous lustre and white streak. It is brittle with an uneven fracture, and the estimated Mohs hardness is 3½ to 4. The calculated density is 5.007 g/cm³. Optically, gysinite-(La) is biaxial (–), α= 1.832(2), β= 1.849(4), γ = 1.862(5) in white light and 2V_meas = 81.6°. The empirical formula of gysinite-(La) is (La_0.93Pb_0.61Nd_0.23Pr_0.14Sr_0.04Gd_0.02Sm_0.01Eu_0.01Ca_0.01)_Σ2(CO₃)₂(OH)_1.34⋅0.66H₂O, which is calculated on the basis of general formula (REE_xM²⁺_2–x)(CO₃)₂(OH)_x⋅(2–x)H₂O. The strongest eight lines of its powder X-ray diffraction pattern [d, Å (I, %) (hkl)] are: 5.596 (21) (011), 4.349 (100) (110), 3.732 (68) (111), 2.984 (61) (121), 2.667 (21) (031), 2.363 (48) (131), 2.090 (29) (221) and 2.028 (21) (212). Gysinite-(La) is orthorhombic, in the space group Pmcn, and unit-cell parameters refined from single-crystal X-ray diffraction data are: a = 5.0655(2) Å, b = 8.5990(3) Å, c = 7.3901(4) Å, V = 321.90(2) ų and Z = 2. It is a new member of the ancylite group and isostructural with gysinite-(Nd), but with La and Pb dominant in the metal cation sites in the structure.

Fluorsigaiite, ideally Ca₂Sr₃(PO₄)₃F, is a new Sr analogue of fluorphosphohedyphane and a new member of the apatite supergroup. It was discovered in lujavrite from the Saima alkaline complex, Liaoning Province, China. Fluorsigaiite commonly occurs as individual prismatic, columnar and platy crystals of 10 to 50 μm in size, associated with microcline, nepheline, aegirine, natrolite, eudialyte, fluorapatite, a fluorstrophite-like mineral, stronadelphite and calcite. Occasionally, crystals of fluorsigaiite form prismatic aggregates in the interstices of lujavrite. Fluorsigaiite is translucent to transparent, colourless to yellowish white with a vitreous lustre and without fluorescence. The estimated Mohs hardness is 5, and the tenacity is brittle with uneven fractures. The calculated density is 3.842 g/cm³. Optically, fluorsigaiite is uniaxial (–) with ω = 1.64(1) and ɛ = 1.63(1) in white light and without dispersion. The mean chemical composition (in wt.%) of fluorsigaiite is Na₂O 0.75, CaO 15.17, SrO 44.44, La₂O₃ 3.64, Ce₂O₃ 2.22, Pr₂O₃ 0.19, Nd₂O₃ 0.13, Sm₂O₃ 0.05, Gd₂O₃ 0.23, P₂O₅ 31.87, F 1.91, H₂O 0.46, sum 100.26, giving the empirical formula (Sr_2.82Ca_1.79Na_0.16La_0.15Ce_0.09Pr_0.01Nd_0.01Gd_0.01)_Σ5.04P_2.97O₁₂[F_0.66(OH)_0.34]_Σ1, which is calculated on the basis of 13 total anions and F+(OH) = 1. The strongest eight lines of its powder X-ray diffraction pattern [d, Å (I, %) (hkl)] are: 3.563 (15) (002), 3.275 (15) (102), 3.144 (19) (120), 2.876 (100) (121), 2.861 (96) (112), 2.772 (27) (300), 1.991 (17) (222) and 1.895 (23) (213). Fluorsigaiite is hexagonal, in the space group P6₃/m and unit-cell parameters refined from single-crystal X-ray diffraction data are: a = 9.6101(2) Å, c = 7.1311(1) Å, V = 570.35(3) ų and Z = 2. It is isostructural with hedyphane-group minerals, and contains different prevailing (species-defining) Ca and Sr cations at the Ca1 and Ca2 sites, respectively. Fluorsigaiite was probably formed from Sr-rich fluids at late-magmatic or hydrothermal stage of the Saima lujavrite.

Plumbogaidonnayite, ideally PbZrSi₃O₉⋅2H₂O, is a new gaidonnayite-group mineral discovered as a secondary product derived from the alteration of eudialyte from the Saima alkaline complex, China. It occurs as aggregates (up to 1 mm) composed of subhedral to anhedral or platy crystals (individually 5–50 μm), associated closely with microcline, natrolite, aegirine, gaidonnayite, georgechaoite, zircon, bobtraillite and britholite-(Ce) in eudialyte pseudomorphs. The crystals are transparent, colourless or light brown with a vitreous lustre. Plumbogaidonnayite is brittle with conchoidal fracture, and it has a Mohs hardness of ~5 and a calculated density of 3.264 g/cm³. It is optically biaxial (+) with α = 1.61(3), β = 1.63(3) and γ = 1.66(4). The calculated 2V is 80°, with the optical orientations X, Y and Z parallel to the crystallographic a, b and c axes, respectively. The empirical formula is (Pb_0.70Ca_0.17Ba_0.01K_0.11Na_0.01Y_0.01)_Σ1.01(Zr_1.00Hf_0.01Ti_0.01)_Σ1.02Si_3.01O₉⋅2H₂O calculated on the basis of nine oxygen atoms per formula unit and assuming the occurrence of two H₂O groups. Plumbogaidonnayite is orthorhombic, P2₁nb, a = 11.7690(4) Å, b = 12.9867(3) Å, c = 6.66165(16) Å, V = 1018.17(5) ų and Z = 4. The nine strongest lines of its powder XRD pattern [d in Å (I, %) (hkl)] are: 6.489 (36) (020), 5.803 (100) (101), 4.661 (27) (021), 4.336 (29) (121), 3.640 (30) (221), 3.114 (79) (112), 2.947 (27) (400), 2.622 (27) (241) and 2.493 (27) (312). Plumbogaidonnayite has a similar spiral chain framework structure with gaidonnayite and georgechaoite, which is composed of SiO₄ tetrahedra and ZrO₆ octahedra, but with disordered extra-framework sites (cations and H₂O groups) characterised by the substitution of 2Na⁺ (K⁺)→Pb²⁺ (Ca²⁺) + □ (vacancy). The discovery of plumbogaidonnayite adds a new perspective on the cation ordering and heterovalent substitution mechanism in gaidonnayite-group minerals.