Search Results (63)

The Weishan rare earth element (REE) deposit, located in western Shandong, North China Block, is a typical carbonatite REE deposit and constitutes the third largest light REE resource in China. Its mineralization is closely related to the multi-stage evolution of a carbonatite magma–hydrothermal system. However, the mechanisms governing REE enrichment, migration, and precipitation remain insufficiently constrained from a mineralogical perspective, which hampers the understanding of the ore-forming processes and the establishment of predictive exploration models. Apatite is a pervasively developed REE phase in the Weishan deposit which occurs in multiple generations, and thus represents an ideal recorder of the magmatic–hydrothermal evolution. In this study, different generations of apatite hosted in carbonatite orebodies from the Weishan deposit were investigated using cathodoluminescence (CL), electron probe microanalysis (EPMA), and in situ LA-ICP-MS trace element analysis. Three types of apatite were identified. In paragenetic sequence, Ap-1 occurs as polycrystalline aggregates coexisting with calcite, is enriched in Na, Sr, and LREEs, and shows high (La/Yb)_N ratios, suggesting crystallization from an evolved carbonatite magma. Ap-2 and Ap-3 display typical replacement textures: both contain abundant dissolution pits and dissolution channels within the grains, which are filled by secondary minerals such as monazite and ancylite, and thus exhibit characteristic features of fluid-mediated dissolution–reprecipitation during the hydrothermal stage. Ap-2 is commonly associated with barite and strontianite, whereas Ap-3 is associated with pyrite and monazite and is characterized by relatively sharp grain boundaries with adjacent minerals. From Ap-1 to Ap-3, total REE contents decrease systematically, whereas Na, Sr, and P contents increase. All three apatite types lack Eu anomalies but display positive Ce anomalies. Discrimination diagrams involving LREE-Sr/Y and log(Ce)-log(Eu/Y) indicate that apatite in the Weishan REE deposit formed during the magmatic to hydrothermal evolution of a carbonatite, and that the dissolution of early magmatic apatite, followed by element remobilization and mineral reprecipitation, effectively records the progressive evolution of the ore-forming fluid. Full article

Fluorite, a key accessory mineral associated with rare earth element (REE) deposits, exerts a significant influence on REE migration and precipitation through complexation, adsorption, and lattice substitution within fluorine-bearing fluid systems. It therefore provides a valuable archive for constraining REE enrichment processes. The Weishan alkaline–carbonatite-related REE deposit, the third-largest LREE deposit in China, is formed through a multistage magmatic–hydrothermal evolution of the carbonatite system. However, limited mineralogical constraints on REE enrichment and precipitation have hindered a comprehensive understanding of its metallogenic processes and exploration potential. Here, cathodoluminescence imaging and LA-ICP-MS trace element analyses were conducted on fluorite of multiple generations from the Weishan deposit to constrain the physicochemical conditions of mobility and precipitation mechanisms of this REE deposit. Four generations of fluorite are recognized, recording progressive evolution of the ore-forming fluids. Type I fluorite, which coexists with bastnäsite and calcite, is LREE-enriched and exhibits negative Eu anomalies, indicating precipitation from high-temperature, weakly acidic, and reducing fluids. Type II fluorite occurs as overgrowths on Type I, while Type III fluorite replaces Type II fluorite, with both displaying LREE depletion and MREE-Y enrichment, consistent with cooling during continued hydrothermal evolution. Type IV fluorite, which is interstitial between calcite grains and associated with mica, is formed under low-temperature, oxidizing conditions, reflecting REE exhaustion and the terminal stage of fluorite precipitation. Systematic shifts in REE patterns among the four generations track progressive cooling of the system. The decreasing trend in La/Ho and Tb/La further suggests that these fluorites record dissolution–reprecipitation events and associated element remobilization during fluid evolution. Full article

Rare earth elements (REEs) are essential for modern high-tech development and have been identified as key mineral resources by major economies worldwide. This paper presents a systematic review of REE deposits in Africa, covering their distribution, reserves and resources, deposit types, mineralization ages, characteristics of typical deposits, and exploration investments. Africa hosts abundant REE resources, which are primarily concentrated in 12 countries. The continent’s reserves and advanced resources of rare earth oxides (REO) amount to 195.6 × 10⁴ t and 1014.4 × 10⁴ t, respectively. In recent years, exploration and development efforts have progressed rapidly. REE mineralization in Africa can be classified into eight categories, with carbonatite and ion-adsorption-type deposits currently being the primary focus of exploration and development. Exploration investment in African REE deposits peaked in 2012, followed by a decline to its lowest point in 2017. Since 2018, the exploration investment value has increased rapidly. Looking ahead, prices for light rare earth elements (LREEs) are projected to stabilize or experience a slight decrease, while prices for heavy rare earth elements (HREEs) are expected to gradually increase. Full article

Rare earth elements (REYs) are crucial components of billions of products worldwide. Transitioning from foreign to domestic REY sources requires utilizing both primary (i.e., carbonatites, alkaline igneous rocks, pegmatites, skarn deposits) and secondary (unconventional) sources (i.e., ion-adsorption clays, placer deposits, weathered rock, black and/or oil shales). Coal and coal-bearing strata, promising secondary REY resources, are the focus of this study. Understanding REY mineral associations in unconventional resources is essential to quantifying resource volume and identifying viable mineral separation and processing techniques. Highly REY-enriched (>750 ppm) coal or mudstone samples from the Uinta Region, Utah, USA, were selected for scanning electron microscopy (SEM) analysis. Energy dispersive X-ray spectroscopy (EDS)-determined REY enrichment occurs in: (1) a silt-size fraction (5–30 μm) of monazite and xenotime REY-enriched grains, (2) a clay-size fraction (2–5 μm) of monazite REY-enriched grains dispersed in the clay-rich matrix, and (3) organically confined REY domains < 2 μm. Findings suggest possible REY enrichment from multiple sources, including: (1) detrital silt-size grains, (2) volcanic ash fall, largely in clay-size grains, and (3) organic REY uptake in the peat swamp depositional environment. Full article

Rare earth elements (REEs), as necessary elements in many industries, have driven increased demand for mineral exploitation. However, understanding the occurrence states of REEs is crucial for their extraction. Therefore, this work primarily investigated the differences in the occurrence states of REEs and the thermal decomposition behavior of carbonatite rare earth deposits in China using scanning electron microscopy, Fourier transform infrared spectroscopy, X-ray powder diffraction, and X-ray photoelectron spectroscopy. The results showed that the bastnaesite concentrate from the M deposit in southwestern China (referred to herein as B-ore), contained REEs accounting for 53.59%, and was associated with small amounts of wulfenite, barite, and iron ore. In contrast, the contents of REEs in the raw ores of N deposit in northern China (referred to herein as R-ore) was relatively low (3.71%), but were also enriched in Fe. R-ore consisted of small particle, with 32.44% sized between 0.075 and 0.11 mm, and 26.38% below 0.075 mm. The contents of Fe, La, and Ce in these smaller particles were higher than those of larger particles. Fe might be substituted with Ce, La, and other REEs in magnetite crystals, forming isomorphic structures. This research was expected to provide assistance in the efficient extraction of REEs from carbonatite deposits. Full article

Alkaline carbonatite complexes are formed by magmatic, hydrothermal, and weathering geological events, which modify the minerals present in the rocks, resulting in ores with varied metallurgical behavior. To better spatially distinguish ores with distinct plant responses, creating a 3D geometallurgical block model was necessary. To establish the clusters, four different algorithms were tested: K-Means, Hierarchical Agglomerative Clustering, dual-space clustering (DSC), and clustering by autocorrelation statistics. The chosen method was DSC, which can consider the multivariate and spatial aspects of data simultaneously. To better understand each cluster’s mineralogy, an XRD analysis was conducted, shedding light on why each cluster performs differently in the plant: cluster 0 contains high magnetite content, explaining its strong magnetic yield; cluster 3 has low pyrochlore, resulting in reduced flotation yield; cluster 2 shows high pyrochlore and low gangue minerals, leading to the best overall performance; cluster 1 contains significant quartz and monazite, indicating relevance for rare earth elements. A hierarchical indicator kriging workflow incorporating a stochastic partial differential equation (SPDE) trend model was applied to spatially map these domains. This improved the deposit’s circular geometry reproduction and better represented the lithological distribution. The elaborated model allowed the identification of four geometallurgical zones with distinct mineralogical profiles and processing behaviors, leading to a more robust model for operational decision-making. Full article

Rare-earth elements (REEs), including lanthanides, scandium, and yttrium, are important for advanced technologies such as renewable energy systems, electronics, medical diagnostics, and precision agriculture. Despite their relative crustal abundance, REE extraction is impeded by complex geochemical behavior, dispersed distribution, and environmental challenges. This review presents a comprehensive overview of REE geochemistry, mineralogy, and major deposit types including carbonatites, alkaline igneous rocks, laterites, placer deposits, coal byproducts, and marine sediments. It also highlights the global distribution and economic potential of key REE projects. The integration of machine learning has further enhanced exploration by enabling deposit classification and geochemical modeling, especially in data-limited regions. Environmental and health challenges associated with REE mining, processing, and electronic waste (e-waste) recycling are studied, along with the expanding use of REEs in agriculture and medicine. Some recycling efforts offer promise for supply diversification, but significant technological and economic barriers remain. Ensuring a secure and sustainable REE supply will require integrated approaches combining advanced analytics, machine learning, responsible extraction, and coordinated policy efforts. The present review offers a general overview that can be useful for informing future studies and resource-related discussions. Full article

Türkiye hosts a wide variety of barite deposits that can be broadly classified into two major groups based on their tectonic settings: magmatism-associated and passive margin-hosted deposits. The magmatism-associated deposits include Kızılcaören (F + Ba + REE + Th, Beylikova–Eskişehir), Kirazören (Bulancak–Giresun), and Karacaören (Mesudiye–Ordu). The Kızılcaören deposit formed in relation to the emplacement of a late Oligocene carbonatitic sill, while the Kirazören and Karacaören deposits are associated with the Cretaceous Pontide magmatic arc. Passive margin-hosted deposits occur within various Paleozoic sedimentary lithologies—such as metasandstone, shale, schist, and limestone—and are found in the Taurides and the Arabian Platform. These deposits occur as either concordant or discordant veins. This barite belt extends from Şarkikaraağaç (Isparta), through Hüyük (Konya) and Alanya (Antalya), to Silifke (Mersin), Tordere (Adana), Önsen, Şekeroba (Kahramanmaraş), and Hasköy (Muş). The Paleozoic deposits represent the major barite resources of Türkiye, with an annual production of approximately 300,000 metric tons. Smaller deposits around Gazipaşa (Antalya) contain minor Pb-Zn sulfides. Mesozoic barite deposits are hosted in Triassic dolomites and are associated with Pb-Zn mineralization in the Hakkari region of the Arabian Platform. Pb and Sr isotope data indicate that the barium in these deposits was derived from ancient continental crust. The isotopic compositions of both concordant (stratabound) and discordant (vein-type) barites are generally homogeneous. In northwestern Türkiye, the Sr isotope compositions of the barite deposits align well with those of the Oligocene carbonatite host complex. The ⁸⁷Sr/⁸⁶Sr isotope ratio of the Kızılcaören deposit (0.706‰) is the least radiogenic among Turkish barite deposits, suggesting a mantle contribution. The Kirazören deposit in the Pontide magmatic arc follows with a slightly higher ratio (0.707‰). Triassic barites from the Hakkari region yield ⁸⁷Sr/⁸⁶Sr values around 0.709‰, slightly more radiogenic than coeval seawater. Paleozoic barite deposits show the most radiogenic ⁸⁷Sr/⁸⁶Sr values, including Aydıncık (0.718‰), Şarkikaraağaç (0.714‰), Hasköy (0.713‰), Kahramanmaraş (0.712‰), Tordere, and Hüyük (both 0.711‰), consistent with their respective host rocks. The elevated radiogenic Pb and Sr isotope values in the passive margin-hosted deposits suggest that the barium originated from deeper, barium-enriched rocks, whereas stable sulfur isotope data point to a marine sulfur source. Moreover, Sr and S isotopic signatures indicate that the Paleozoic sediment-hosted deposits formed in association with cold seeps on the seafloor, resembling modern analogs. In contrast, the Mesozoic Karakaya deposit (Hakkari) represents a typical vent-proximal, sediment-hosted deposit with no magmatic signature. Full article

The Bayan Obo deposit, located on the northern margin of the North China Plate (NCP), is the world’s largest comprehensive Fe-REE-Nb deposit. After its formation, this deposit was affected by multiple tectonic thermal events, but the ages of these geological events are controversial. To determine the evolutionary history of the Bayan Obo deposit, we conducted a detailed study of the macroscopic and microscopic deformation characteristics of the ore district and selected representative minerals, such as riebeckite and biotite, which are widely present in the banded rocks of the deposit, for an ⁴⁰Ar-³⁹Ar isotopic analysis. The results show that a large number of deformation structures have developed in the carbonatite and surrounding rocks, including mineral bands, boudins, tight folds, and rotated porphyroclasts, suggesting that the region has undergone intense compression and shearing and that the deformation temperature can reach ~550 °C. ⁴⁰Ar-³⁹Ar plateau ages of 414.9 ± 1.4 Ma and 264.5 ± 2.5 Ma were obtained for the riebeckite and biotite, respectively. Using these results in conjunction with regional geological data and considering the closure temperature of the mineral isotope system, it was inferred that these two ages corresponded to two distinct reworking events experienced by the deposit during the Early Paleozoic and Late Paleozoic following its initial formation. These events corresponded to the collision between the Bainaomiao Arc and the NCP and the magmatic activity induced by a continental–continental collision during the closure of the Paleo-Asian Ocean (PAO), respectively. Full article

Apatite and rare earth elements (REEs) are vital to the European Union’s economic growth and resource security, given their essential roles in fertilizers, green technologies, and high-tech applications. To meet rising demand and reduce reliance on imports, the exploitation of domestic deposits has become increasingly important. This study investigates the beneficiation potential of ore from a carbonatite complex (Finland), focusing on the recovery of fluorapatite concentrate through froth flotation. This research addresses two key objectives: evaluating the potential for REE enrichment alongside fluorapatite concentration using conventional anionic and amine-based reagents, and assessing separation efficiency when partially substituting the most effective conventional collectors with bio-based organosolv lignin nanoparticles. Adequate recovery rates for apatite and REEs were achieved using common anionic collectors, such as hydroxamate and sarcosine, yielding P grades of 23.4% and 21.5%, and recoveries of 96.4% and 89.2%, respectively. Importantly, concentrate quality remained stable with up to a 30% reduction in conventional collectors and the addition of organosolv lignin. Bench-scale trials further validated the approach, demonstrating that lanthanum and cerium recoveries exceeded 71%, alongside satisfactory apatite recovery. Lignin nanoparticles were observed to interact with both minerals; however, the interaction was more pronounced in the case of phlogopite, which exhibited a markedly greater increase in surface hydrophilicity following treatment, suggesting a stronger affinity or surface modification effect, which was beneficial to the performance of the separation process. Full article

A variety of variables, such as organic matter input, redox conditions, depositional rates, and terrigenous input, affect the deposition of black shale. Furthermore, because of the significant regional variations in paleodepositional environments, these factors have a complex role in organic matter enrichment. Global geological events influenced sedimentary conditions, organic enrichment, and the development of organic-enriched shales during the Late Ordovician to Early Silurian. The Wufeng–Longmaxi Formation black shales in Southeastern Chongqing were analyzed for X-ray diffraction (XRD), major and trace element geochemistry, and total organic carbon (TOC) data; this led to further analysis of the relationship between the depositional environment and organic matter aggregation and rock type evolution. The primary minerals found in the Wufeng–Longmaxi shale are quartz, feldspar, carbonatite (calcite and dolomite), and clay. The high index of compositional variability (ICV) values (>1) and the comparatively low chemical index of alteration (CIA) values (52.6–72.8) suggest that the sediment source rocks are juvenile and are probably experiencing weak to moderate chemical weathering. The selected samples all show negative Eu anomalies, flat heavy rare earth elements, and mildly enriched light rare earth elements. The ratios of La/Th, La/Sc, Th/Sc, ΣREE-La/Yb, TiO₂-Ni, and La/Th-Hf suggest that acidic igneous rocks were the main source of sediment, with minor inputs from ancient sedimentary rocks. The correlations of paleoclimate proxies (Sr/Cu, CIA), redox proxies (V/Cr, V/Ni, V/(V + Ni), Ni/Co, U/Th), paleoproductivity proxies (Ba_xs, Cu_EF, Ni_EF), and water mass restriction proxies (Mo/TOC, U_EF, Mo_EF) suggest a humid–semiarid, anoxic, moderate–high paleoproductivity, and moderate–strongly restricted environment. On the basis of the aforementioned interpretations, the paleoenvironment of the Wufeng–Longmaxi Formations was established, with paleoredox conditions and restricted water masses likely being the primary factors contributing to organic matter enrichment. Full article

The Mesoproterozoic alkaline Grønnedal-Íka complex (1325 ± 6 Ma) is intruded into old Archean gneissic bedrock between Ikka Fjord and Kangilinnguit (Grønnedal) by Arsuk Fjord in Southwestern Greenland. This 8 × 2.8 km oval-shaped complex constitutes the oldest part of the Gardar Province, representing a failed continental rift across southern Greenland. It comprises outer rings of mainly nepheline syenites with a central plug of Fe- and Ca-rich carbonatites. Here, we present petrological data on the syenites and carbonatites combined with geochemical modelling of groundwater percolating through the Grønnedal-Íka complex and the secondary minerals and fluid chemistry arising from these fluid–rock reactions. The results show that modelling using input data of (1) meteoric water in a closed system with respect to atmospheric CO₂ can (2) dissolve the primary minerals of the syenites and carbonatites and (3) simulate the fluid chemistry of the natural sodium carbonate springs of 3–4 °C and pH 10–11 seeping up through fractures at the bottom of Ikka Fjord, which (4) leads to the deposition of nearly a thousand tufa columns of the cold carbonate mineral ikaite (CaCO₃•6H₂O). Our results thereby support the geochemical relationship between fluid–rock reactions inside the Grønnedal-Íka alkaline complex and the precipitation of ikaite in the shape of submarine tufa columns in Ikka Fjord. The modelling indicates that the groundwater itself can be supersaturated with respect to ikaite and provide the seed crystals that lead to the columnar growth of ikaite up to 20 m tall in the seawater of Ikka Fjord. Full article

The Bayan Obo is the largest carbonatite-type rare earth deposit in the world. It not only has a large amount of light rare earth element (LREE) resources but also hosts approximately 9 million tons of medium and heavy rare earth element (M+HREE) resources. However, the M+HREE resources have not received enough attention, which hinders their further utilization. In this study, we conduct a systematic investigation of the distribution and process mineralogy properties of M+HREE in different types of ores in the Bayan Obo deposit. The high-value area (>0.1%) of M+HREE elements is found concentrated in the central and deeper parts of the Main and East orebodies. The content of M+HREE varies among different types of ores, with the Aegirine type (1005 ppm) and Fluorite type (1204 ppm) showing a higher average M+HREE concentration. The minerals rich in M+HREE include bastnäsite, monazite, Ca-fluorocarbonate, Ba-fluorocarbonate, allanite, aeschynite, and fergusonite, each with concentrations exceeding 4000 ppm. Aeschynite and fergusonite, in particular, exhibit high M+HREE concentrations and are enriched in fluorite-type and aegirine-type ores. Analysis of the mixed raw ores from the production line at the concentrating plant reveals an M+HREE concentration of approximately 0.2% and a concentration of the seven target minerals at around 12%. However, the particle size distribution and monomer dissociation degree are limited to below 22.3 µm and 40%, respectively. Based on these integrated analyses, we propose that the fluorite-type and aegirine-type ores within the Main and East open-pits are potential M+HREE targets. Furthermore, the recycling and utilization of M+HREE resources in the Bayan Obo deposit require a well-structured process flow and the selection of advanced processing equipment in the future. Full article

Nioboixiolite-(□) is a new mineral found in a carbonatite sill from the Bayan Obo mine, Baotou City, Inner Mongolia, China. It occurs as anhedral to subhedral grains (100 to 500 μm in diameter) that are disseminated in carbonatite rock composed of dolomite, calcite, magnetite, apatite, biotite, actionlike, zircon, and columbite-(Fe). Most of these grains are highly serrated, with numerous inclusions of columbite-(Fe). The mineral is gray to deep black in color; is opaque, with a semi-metallic luster; has a black streak; and is brittle, with an uneven conchoidal splintery. The Mohs hardness is 6–6½, and the calculated density is 6.05 g/cm³. The reflection color is gray with a blue tone, and there is no double reflection color. The measured reflectivity of nioboixiolite-(□) is about 10.6%~12.1%, close to that of ixiolite (11%–13%). Nioboixiolite-(□) is non-fluorescent under 254 nm (short-wave) and 366 nm (long-wave) ultraviolet light. The average chemical analysis results (wt.%) of twelve electron microprobe analyses are F 0.01, MnO 0.12, MgO 0.15, BaO 0.62, PbO 0.91, SrO 1.49, CaO 2.76, Al₂O₃ 0.01, TREE₂O₃ 1.58, Fe₂O₃ 3.57, ThO₂ 0.11, SiO₂ 1.69, TiO₂ 3.68, Ta₂O₅ 13.95, Nb₂O₅ 47.04, and UO₃ 21.56, with a total of 99.25. The simplified formula is [Nb⁵⁺, Ta⁵⁺,Ti⁴⁺, Fe³⁺,□,]O₂. X-ray diffraction data show that nioboixiolite-(□) is orthorhombic, belonging to the space group Pbcn (#60). The refined unit cell parameters are a = 4.7071(5) Å, b = 5.7097(7) Å, c = 5.1111(6) Å, V = 138.31(3), and β = 90(1) °Å³ with Z = 4. In the crystal structure of nioboixiolite-(□), all cations occupy a single M1 site. In these minerals, edge-sharing M₁O₆ octahedra form chains along the c direction. In this direction, the chains are connected with each other via common vertices of the octahedra. The strongest measured X-ray powder diffraction lines are [d in Å, (I/I0), (hkl)]: 3.662(20) (110), 2.975(100) (111), 2.501(20) (021), 1.770(20) (122), 1.458(20) (023). A type specimen was deposited in the Geological Museum of China with catalogue number M16118, No. 15, Yangrou Hutong, Xisi, Beijing 100031, People’s Republic of China. Full article

Situated throughout the southeastern United States within the Laurentian craton are occurrences of various aged deposits (Late Proterozoic to Early Paleogene) that contain volcanics spanning from lamprophyres to carbonatites and basalts to rhyolites. Several are intrusive, while others have been reworked detritally, deposited as river gravels out onto the Gulf Coastal Plain. The earliest occurrence of igneous gravel clasts in the coastal plain of the lower Mississippi Valley lie along the Mississippi River’s eastern valley wall in the ancestral Mississippi River’s pre-loess terrace deposits (PLTDs). The coarse clastics of the PLTDs are dominantly chert gravels derived from Paleozoic carbonate bedrock, but also include clasts of Precambrian Sioux Quartzite, glacially faceted and striated stones, and ice-rafted boulders, which indicate a direct relationship between the PLTDs and glacial outwash during the cyclic glaciation of the Pleistocene Epoch. The PLTDs also contain the oldest known examples of igneous gravels exposed at the surface in Mississippi. An understanding of their igneous bedrock provenance and the timing of their contribution to the sedimentary record of the lower Mississippi River Valley sheds a valuable light onto the geologic history and evolution of the ancestral Mississippi River during the Pleistocene Epoch. The use of fusion inductively coupled plasma mass-spectroscopy (ICP-MS) in the identification of the igneous suites of one of the pre-loess terraces, well-delineated by geologic mapping, adds important geochemical source data from the gravel constituents for the further interpretation and correlation of the individual PLTD allounits. Gravel constituent geochemistry also offers a better understanding of the evolution of the ancestral Mississippi River watershed and the contributions of bedrock sources during Pleistocene glaciation. This petrological study suggests that the igneous gravels sampled from within the Rawhide PLTD allounit originated from the St. Francois Mountains (SFMs) in southwestern Missouri, with the implications that the SFM igneous terrain was in the direct path of the Independence “Kansan” glaciation. This could indicate a glacial extent further southwest than previously documented. Full article