Nb–Ta mineralization in Ti-oxide minerals from the Bagolyhegy Metarhyolite Formation (Bükk Mountains, NE Hungary)

The foliated low-grade metamorphic rocks of the Triassic Bagolyhegy Metarhyolite Formation, mainly of pyroclastic origin, host post-metamorphic quartz-albite veins containing abundant tourmaline and occasionally rutile/ilmenite. The study of the Ti-oxide-mineralized veins with SEM-EDX revealed an unusual mineral assemblage comprising fine-grained Nb–Ta-bearing oxides (columbite-tantalite series, fluorcalciomicrolite and other Nb–Ti–Y–Fe-REE-oxide minerals) intergrown with Nb-rich polymorphs of TiO2 (anatase, rutile), ilmenite and zircon enriched with hafnium. This high field strength elements (HFSE)-bearing paragenesis is unexpected in this lithology, and was not described from any formation in the Paleozoic-Mesozoic rock suite of the Bükk Mountains (NE Hungary) before. The host metavolcanics are significantly depleted in all HFSE compared to the typical concentrations in felsic volcanics and the mineralized quartz-albite veins have even lower Ti–Nb–Ta concentration than the host rock, so the mineralization does not mean any enrichment. From proximal outcrops of the Triassic Szentistvánhegy Metavolcanics, potassic metasomatized lenses with albite-quartz vein fillings containing rutile/ilmenite are known. We studied them for comparison, but they only contain REE mineralization (allanite-monazite-xenotime); the Nb–Ta-content of Ti-oxide minerals is undetectably low. LA-ICP-MS measurements for U–Pb dating of Hf-rich zircon of the Nb–Ta-rich mineral assemblage gave 71.5 ± 5.9 Ma as lower intercept age while dating of allanite of the REE mineralized quartz-albite veins gave 113 ± 11 Ma as lower intercept age. The REE-bearing vein fillings formed during a separate mineralization phase in the Early Cretaceous, while the Nb–Ta mineralization was formed by post-metamorphic alkaline fluids in the Late Cretaceous., controlled by fault zones and fractures.

FEASIBILITY OF VISIBLE SHORT-WAVE INFRARED REFLECTANCE SPECTROSCOPY TO CHARACTERIZE REGOLITH-HOSTED RARE EARTH ELEMENT MINERALIZATION

Regolith-hosted rare earth element (REE) deposits predominate global resources of heavy REEs. Regoliths are underlain by various types of igneous rocks and do not always host economically valuable deposits. Thus a feasible and convenient method is desired to identify REE mineralization in a particular regolith. This study presents a detailed visible short-wave infrared reflectance (VSWIR) spectroscopic study of the Renju regolith-hosted REE deposit, South China, to provide diagnostic parameters for targeting REE orebodies in regoliths. The results show that the spectral parameters, M794_2nd and M800_2nd, derived from the VSWIR absorption of Nd3+ at approximately 800 nm, can be effectively used to estimate the total REE concentrations in regolith profiles. M1396_2nd/M1910_2nd ratios can serve as proxies to evaluate weathering intensities in a regolith. Abrupt changes of specific spectral features related to mineral abundances, chemical compositions, and weathering intensities can be correlated with variations of protolith that formed a regolith. These VSWIR proxies are robust and can be used for exploration of regolith-hosted REE deposits.

Thorium, uranium and rare earth mineralization in rocks of the Ugakhan gold deposit, Bodaibo ore region (Irkutsk oblast)

The paper reports on the results of studies of ore-bearing rocks of the Ugakhan gold deposit (Bodaybo district): metasandstones, metasiltstones and carbonaceous shales. The rocks consist of quartz, feldspar (albite, orthoclase), Fe-Mg chlorite, mica (muscovite, sericite) and carbonates (calcite, dolomite, anker-ite) and accessory titanite, rutile, tourmaline, zircon and apatite. All rocks contain fragments of microfossils exhibiting striking concentric zonation with alternated dark (carbonaceous matter) and light (carbonate-mica material) layers. In a range from metasandstones to carbonaceous shales, the rocks exhibit an increase in mica amount and the content (up to 3%) of carbonaceous matter, as well as the formation of regeneration rims around relict tourmaline and zircon. The REE mineralization includes silicates (REE-bearing epidote, thorite), fuorocarbonates (bastnesite) and phosphates (monazite, xenotime, ankylite), which are closely related to U minerals (uraninite, cofnite). Bastnesite, ankylite and thorite formed due to the decomposition of earlier REE-bearing epidote, whereas monazite and xenotime are the products of decomposition of apatite. Uraninite formed during lithifcation of matrix of carbon-bearing rocks and is replaced by cofnite. The thermal analysis of carbonaceous matter and the formation temperature of chlorite calculated using chlorite geothermometer (296–371 °С) indicate the transformation of rocks under conditions of sericite-chlorite subfacies of greenschist facies of metamorphism.