Search Results (5)

Titanite is widely used in geochronology and petrogenetic studies, yet its behaviour during fluid-mediated alteration remains insufficiently constrained. This study investigates titanite alteration and element redistribution in the Mesoproterozoic Kabeliai granitoids (southern Lithuania) to evaluate their response to magmatic and hydrothermal processes. Petrography, EPMA, LA-ICP-MS, U-Pb geochronology, and mass balance modeling were combined to characterise titanite textures, chemistry, and isotopic evolution. Three titanite types were distinguished. Type 1 titanite preserves magmatic compositions and yields U-Pb ages of 1508 ± 19 (MSWD = 0.91; 2σ) and 1527 ± 9 Ma (MSWD = 0.54; 2σ), consistent with late magmatic crystallisation. Type 2 titanite represents a transitional fluid-altered stage, characterised by a porous texture. Type 3 titanite is interpreted to record hydrothermal recrystallisation, trace element depletion (Y, REE, Nb, Zr), and U-Pb resetting, with ages of 1454 ± 14 Ma (MSWD = 0.48; 2σ) and 1475 ± 23 Ma (MSWD = 0.63; 2σ) partially overlapping molybdenite mineralisation at ca. 1486 Ma. Mass balance modeling indicates that alteration was dominated by coupled albitisation and chloritisation, and by the redistribution of Ca, Si, and REE. In contrast, Ti remained relatively immobile at the rock scale and was locally redistributed among secondary phases via dissolution–reprecipitation. These results suggest that different titanite domains may preserve distinct stages of magmatic and hydrothermal evolution and highlight the importance of microstructural context when interpreting U-Pb ages in altered granitoid systems. Full article

In this study, the occurrence and leachability of rare earth elements and yttrium (REY) in medium-rank coal—meta-bituminous B coal from the southwestern part of the Upper Silesian Coal Basin in Poland—were investigated. The coal samples contained variable amounts of siderite, dolomite, calcite, kaolinite, illite, quartz, apatite, and pyrite in their mineral composition. A five-step sequential chemical leaching procedure was used, including deionized water, 3% HCl, 5% HNO₃, 10% HNO₃ with microwave assistance, and concentrated HCl–HF also with microwave assistance. The highest concentrations of ∑REY were observed in seam 404/1. Light REY (LREY) dominated the REY composition (>75%), while heavy REY (HREY) accounted for less than 10%. The chondrite-normalised REY patterns and total REY content indicate a clastic origin of REY-bearing minerals. The most efficient leaching occurred in stages IV and V. The solutions from stages I–III preferentially mobilised critical REY, while those from stages IV–V reflected the REY distribution in the coal. Based on the C_outl index, both coal and leachates from the later stages are classified as prospective REY resources. However, absolute REY concentrations should be considered when interpreting C_outl values. The positive correlation between apatite and kaolinite contents and ∑REE concentrations suggests their role in REY enrichment. Full article

Copper, uranium, and rare earth element (REE) mineralisation occurs in hydrocarbon-bearing Devonian continental sandstones in southwest Orkney, Scotland. The aeolian Yesnaby Sandstone Formation and fluvial Harra Ebb Sandstone Formation were mineralised following oil emplacement. The REE-bearing APS mineral florencite is particularly associated with bituminous nodules, many of which contain brannerite. Subsequently hydrothermal copper and other sulphides, and barite, further mineralised the oil reservoir at a temperature of ~190 °C. Oil was mobilised through mineralised fractures at this stage. Biodegradation of the oil occurred later, following the Carboniferous-Permian uplift. The occurrence confirms that Cu-APS mineralisation is possible in relatively low-temperature regimes in sedimentary basins. Full article

The essential role of Critical Elements (CE) in 21st century economy has led to an increasing demand of these metals and promotes the exploration of non-conventional deposits such as weathering profiles. The present work is focused on the study of a weathering profile located at the Archaeological Park of the Gavà Neolithic Mines, Barcelona, Catalonia, Spain. In the Gavà deposit, acid and oxidising meteoric fluids generated intense weathering during the early Pleistocene, affecting series of Llandoverian black shales and associated syn-sedimentary phosphates. The circulation of these acid fluids at deeper levels of the profile generated supergene vein-like mineralisations comprised of secondary phosphates (e.g., variscite, perhamite, crandallite, phosphosiderite) and sulphates (e.g., jarosite, alunite). This supergene mineralisation is significantly enriched in certain CE (e.g., Ga, Sc, REE, In, Co and Sb) that were mobilised from host rock components and later hosted in the crystal lattice of supergene minerals. Weathering processes and corresponding supergene enrichment of CE at the Gavà deposit could be used as an example to determine exploration guidelines of CE in weathering profiles and associated supergene phosphates worldwide. Full article

Eudialyte-hosted critical metal deposits potentially represent major sources of rare earth elements (REE), zirconium and niobium. Here, we study the chemical and isotopic composition of fresh and altered eudialyte in nepheline syenite from the Ilímaussaq Complex, Greenland, one of the world’s largest known eudialyte-hosted deposits. Late-magmatic hydrothermal alteration caused partial replacement of primary magmatic eudialyte by complex pseudomorph assemblages of secondary Zr-, Nb-, and REE-minerals. Three secondary assemblage types are characterised by the zirconosilicates catapleiite, gittinsite and zircon, respectively, of which the catapleiite type is most common. To investigate elemental exchange associated with alteration and to constrain the nature of the metasomatic fluids, we compare trace elements and Sm/Nd isotope compositions of unaltered eudialyte crystals and their replaced counterparts from five syenite samples (three catapleiite-type, one gittinsite-type, and one zircon-type assemblage). Trace element budgets for the catapleiite-type pseudomorphs indicate a 15–30% loss of REE, Ta, Nb, Zr, Sr and Y relative to fresh eudialyte. Moreover, the gittinsite- and zircon-type assemblages record preferential heavy REE (HREE) depletion (≤50%), suggesting that the metasomatic fluids mobilised high field strength elements. Initial Nd isotope ratios of unaltered eudialyte and catapleiite- and gittinsite-type pseudomorphs are indistinguishable, confirming a magmatic fluid origin. However, a higher initial ratio and stronger HREE depletion in the zircon-type pseudomorphs suggests a different source for the zircon-forming fluid. Although alteration reduces the metal budget of the original eudialyte volume, we infer that these elements re-precipitate nearby in the same rock. Alteration, therefore, might have little effect on overall grade but preferentially separates heavy and light REE into different phases. Targeted processing of the alteration products may access individual rare earth families (heavy vs. light) and other metals (Zr, Nb, Ta) more effectively than processing the fresh rock. Full article