Search Results (11)

Rare earth elements (REEs) are critical mineral resources that play a pivotal role in modern technology and industry. Currently, the global supply of light rare earth elements (LREEs) remains adequate. However, the supply of heavy rare earth elements (HREEs) is associated with substantial risks due to their limited availability. Ion-adsorption type rare earth deposits (IAREDs), which represent the predominant source of HREEs, have become a focal point for exploration activities, with a notable increase in global interest in recent years. This study systematically collected stream sediments and stream water samples from the Jiaping IARED in Guangxi, as well as from adjacent granitic and carbonate background areas, to investigate the exploration significance of geochemical surveys for IAREDs. Additionally, mineralized soil layers, non-mineralized soil layers, and bedrock samples from the weathering crust of the Jiaping deposit were analyzed. The results indicate that stream sediments originating from the Jiaping IARED and granite-hosted background regions display substantially elevated REE concentrations relative to those from carbonate-hosted background areas. Moreover, δEu values in stream sediments can serve as an effective indicator for differentiating weathering products derived from granitic and carbonate lithologies. Within the mining area, three coarse-grained fractions of stream sediments (i.e., +20 mesh, 20–60 mesh, and 60–150 mesh) exhibit REE concentrations comparable to those observed in both granite-hosted and carbonate-hosted background regions. However, the HREEs content in the finer -150-mesh stream sediments from Jiaping IARED is markedly higher than that in the two background regions. The (La/Sm)_N versus (La/Yb)_N ratios of -150-mesh stream sediments in the Jiaping IARED may reflect the mixing processes involving HREE-enriched ore layer, non-mineralized layer, and LREE-enriched ore layer. This observation implies that fine-grained (-150-mesh) stream sediments can partially inherit the REE characteristics of mineralized layers within IAREDs. Scanning electron microscopy (SEM) observations indicate that the enrichment of REEs in fine-grained stream sediments primarily originates from REE-rich accessory minerals derived from parent rocks and mineralized weathering crusts. A comparative analysis reveals that the concentrations of REEs in stream water collected during the rainy season are significantly higher than those collected during the dry season. Moreover, the levels of REEs, especially HREE, in stream water from the Jiaping IARED substantially exceed those in background areas. Collectively, these findings suggest that the geochemical signatures of REEs in rainy season stream water possess diagnostic potential for identifying IAREDs. In conclusion, the integrated application of geochemical surveys of stream water and -150-mesh stream sediments can effectively delineate exploration targets for IAREDs. Full article

Ion-adsorption rare earth deposits are mainly formed by the weathering and leaching of granite ore-forming parent rocks, and heavy rare earth elements (HREEs) are predominantly hosted in this type of deposit. In this study, we focused on the Late Jurassic REE mineralization parent rock, specifically the Shuitou pluton. We employed chronology, petrogeochemistry, and isotope geochemistry to elucidate the REE enrichment process in the granite. The results show that the zircon U–Pb age of the Shuitou pluton is ~150 Ma, and the monazite U–Pb age is ~145 Ma, suggesting that the pluton was formed in the Yanshan Stage. The rocks have high SiO₂ (72.85–75.55 wt%), Al₂O₃ (12.85–14.63 wt%), and K₂O (4.46–5.27 wt%) content, with A/CNK values of 1.05–1.19, differentiation index (DI) values of 87.48–95.59, zircon saturation temperature values of 689–746 °C, Nb/Ta ratios of 2.72–9.54, and Zr/Hf ratios of 7.12–26.11. In addition, the rocks also contain peraluminous minerals such as muscovite and garnet. These characteristics indicate that these rocks belong to highly fractionated S-type granite. The ε_Hf(t) values of zircon and monazite range from −10.04 to −6.78 and from −9.3 to −8.2, respectively, indicating that the magma was primarily derived from Proterozoic metamorphosed sedimentary rocks of crustal origin. In the extensional tectonic setting of South China, a high temperature promotes the melting of REE-enriched accessory minerals, and a higher content of F increases the solubility of REEs in the molten mass. The presence of heavy rare earth minerals, such as garnet, in these rocks contributes to a high content of heavy rare earth elements (HREEs). Additionally, REE-enriched minerals like titanite, bastnaesite, and allanite create the necessary material conditions for the formation of ion-adsorption REE deposits. Full article

Ion-adsorption-type rare-earth element (iREE) deposits, a primary source of global heavy REE (HREE) ores, have attracted wide attention worldwide due to their concentrated distributions and irreplaceable role in the field of cutting-edge technologies. In recent years, iREE mineralization has been reported in the overlying weathering crust of the Mosuoying granites within the Dechang counties, Sichuan Province, Southwest China, suggesting great potential for the formation of iREE deposits. The Mosuoying granites, acting as the primary carrier of REE pre-enrichment, govern the contents and distribution patterns of REEs in their weathering crust. Therefore, investigating the sources and enrichment mechanisms of REEs in the parent rocks will provide a critical theoretical basis for the scientific exploitation and utilization of iREE deposits. In this study, we investigated the migration and enrichment of REEs in the Mosuoying granites (850–832 Ma) using petrography, geochronology, geochemical, and Sr-Nd-Hf isotopic data. The results reveal that the REE enrichment in the Mosuoying granites might be associated with both the melting of crustal felsic rocks and the magmatic-hydrothermal evolution. On the one hand, the granites exhibit different REE patterns. Compared to the light REE (LREE)-rich granites, the HREE-rich granites feature higher SiO₂ contents, higher differentiation index (DI), lower Nb/Ta and Zr/Hf ratios, and more significant negative Eu anomalies, indicating that the crystal fractionation of magmas governed the differentiation of REEs. Furthermore, the hydrothermal fluids further promoted the formation of the HREE-rich granites. On the other hand, the geochemical characteristics suggest that they are A-type granites. Regarding the isotopic characteristics, the Mosuoying granites exhibit negative whole-rock εNd(t) and zircon εHf(t) values, suggesting an evolved crustal source. Therefore, we suggest that the high REE contents in the Mosuoying A-type granites might originate from the partial melting of felsic rocks in a shallow crustal source under high-temperature and low-pressure conditions. Specifically, the high-temperature A-type granitic magmas caused the partial melting of the felsic crustal materials to release REEs; concurrently, these magmas enhanced the solubility of REEs in melt during magmatic evolution, inhibiting the separation of REE-bearing minerals from the melts. These increased the REE contents of the granites. The high-temperature heat source might be associated with the process where the asthenospheric mantle experienced upwelling along slab windows and heated continental crust in the Neoproterozoic extensional setting. Full article

The initial enrichment of rare earth elements (REE) in granites plays an important role for the generation of ion-adsorption type REE deposits. It has been summarized that the mineralization-related granitoids are mostly peraluminous, but the enrichment mechanism of REE in this peraluminous granite is currently not well understood. In this study, we conducted geochronology, petrological, and geochemical investigations on the biotite granite and muscovite granite from the Shangyou complex in Ganzhou, Jiangxi Province. Zircon U-Pb dating indicates that both the biotite granite and muscovite granite generated in the Early Silurian (ca. 433–434 Ma). The high aluminum saturation index and occurrence of muscovite and old zircon cores indicate that they belong to the S-type granite and are derived from the melting of metagreywacke. The relatively higher FeO^T contents, Mg# values, and zirconium saturation temperatures (760–873 °C) for the biotite granite resulted from hydrous melting with the involvement of mantle material. In contrast, the muscovite granite with low FeO^T contents, Mg# values, Nb/Ta ratios, and zirconium saturation temperatures (748–761 °C) indicates a purely crust-derived melt formed by muscovite dehydration melting. There is a positive correlation of REE contents with the formation temperature and Th contents in both the Shangyou granites and the data collected from global peraluminous granites. This indicates that temperature plays a key role in the REE enrichment in peraluminous granites, as the high-temperature condition could promote the melting of REE-rich and Th-rich accessory minerals of allanite and REE-phosphate and result in the increases in both REE contents and Th contents in the melts. Given the fact that the parent granites for ion-adsorbing REE deposits are mostly peraluminous and generated in the extensional setting in South China, we concluded that peraluminous granite formed under high-temperature extensional tectonic settings favors initial REE enrichment, which further contributes to the formation of ion-adsorbing REE deposits in South China. Full article

The ion-adsorption-type rare earth element (iREE) deposits dominantly supply global resources of the heavy rare earth elements (HREEs), which have a critical role in a variety of advanced technological applications. The initial enrichment of REEs in the parent granites controls the formation of iREE deposits. Many Mesozoic and Cenozoic granites are associated with iREE mineralization in the Tengchong block, Southwest China. However, it is unclear how vital the mineralogical and geochemical characteristics of these granites are to the formation of iREE mineralization. We conducted geochronology, geochemistry, and Hf isotope analyses of the Yingpanshan–Damanbie granitoids associated with the iREE deposit in the Tengchong block with the aims to discuss their petrogenesis and illustrate the process of the initial REE enrichment in the granites. The results showed that the Yingpanshan–Damanbie pluton consists of syenogranite and monzogranite, containing REE-bearing accessory minerals such as monazite, xenotime, apatite, zircon, allanite, and titanite, with a high REE concentration (210–626 ppm, mean value is 402 ppm). The parent granites have Zr + Nb + Ce + Y (333–747 ppm) contents and a high FeO^T/MgO ratio (5.89–11.4), and are enriched in Th (mean value of 43.6 ppm), U (mean value of 4.57 ppm), Zr (mean value of 305 ppm), Hf (mean value of 7.94 ppm), Rb (mean value of 198 ppm), K (mean value of 48,902 ppm), and have depletions of Sr (mean value of 188 ppm), Ba (mean value of 699 ppm), P (mean value of 586 ppm), Ti (mean value of 2757 ppm). The granites plot in the A-type area in FeO^T/MgO vs. Zr + Nb + Ce + Y and Zr vs. 10,000 Ga/Al diagrams, suggesting that they are A₂-type granites. These granites are believed to have formed through the partial melting of amphibolites at a post-collisional extension setting when the Tethys Ocean closed. REE-bearing minerals (e.g., apatite, titanite, allanite, and fluorite) and rock-forming minerals (e.g., potassium feldspar, plagioclase, biotite, muscovite) supply rare earth elements in weathering regolith for the Yingpanshan–Damanbie iREE deposit. Full article

Ion-adsorption rare-earth deposits supply over 90% of the global market’s heavy rare-earth elements (HREEs). The genesis of these deposits, particularly HREE deposits, has garnered significant attention. To elucidate the metallogenic mechanisms of HREE deposits, a comprehensive study of the weathering profile of granite was conducted in Jiangxi Province, South China. This study focuses on the following two aspects: the petrogeochemistry of HREE-rich granite and the enrichment and fractionation of rare-earth elements (REEs) during the weathering process. The results suggest that the Dabu granites are a typical peraluminous, high-K, calc-alkaline granite series with high silica content (SiO₂: 74.5%–76.4%), relatively low phosphorus content (P₂O₅: <0.05%), and high HREE content (ΣLREE/ΣHREE: 0.16–0.66). Weathering advances the decomposition of minerals and the release of elements. REEs are mainly fixed in the regolith by scavengers, mainly clays, Fe–Mn oxides, and carbonates, and ΣREE can reach 799 ppm in the B horizon. However, HREEs tend to migrate further and preferentially combine with Fe–Mn oxides and carbonates as compared to LREEs, leading to a significant fractionation of REEs in the regolith (ΣLREE/ΣHREE = 0.2–1.1). Additionally, the differential weathering of REE-bearing minerals and the precipitation of secondary REE-bearing minerals are also vital for REE fractionation. Full article

A number of regolith-hosted REE occurrences have recently been discovered in the Esperance region in southern Western Australia. This paper summarizes major characteristics of REE mineralization and discusses contributing factors and potential controls. The main aim is to explain why there is a lack of highly sought-after ion-adsorption-clay-type REE deposits across the region despite the presence of the regolith-hosted REE mineralization on a regional scale. Local mineralization mostly occurs as continuous flat-lying enrichment “blankets” within the residual regolith developed over Archaean–Proterozoic granite gneisses and granitoids with elevated REE content. The enriched horizon is commonly located in the lower saprolite and saprock and is accompanied by an overlying REE-depleted zone. This distribution pattern, together with the data on HREE fractionation and the presence of the supergene REE minerals, indicates chemogenic type enrichment formed by supergene REE mobilization into groundwater, downward transport, and accumulation in the lower part of the weathering profile. Residual REE accumulation processes due to bulk rock volume and mass reduction during weathering also contribute to mineralization. It is proposed that climate and groundwater chemistry are the critical regional controls on the distribution of REEs in the weathering profile and on their speciation in the enrichment zone. Cenozoic aridification of climate in southwest Australia heavily overprinted pre-existing REE distributions in the weathering profile. Acidic (pH < 4), highly saline groundwaters intensely leached away any relatively weakly bound, adsorbed or colloidal REE forms, moving them downward. Dissolved REEs precipitated as secondary phosphates in neutral to alkaline environment at lower Eh near the base of the weathering profile forming the supergene enrichment zone. Low denudation rates, characteristic of areas of low relief under the arid climate, are favourable for the preservation of the existing weathering profiles with REE mineralization. Full article

Rare earth elements deposited in ion-adsorption clay-type deposits in Northern Kazakhstan were recognised using mineralogical and geochemical methods. The diversity and mineralogical properties of the Shok-Karagay deposit and Syrymbet ore fields under investigation in this study are closely related to the process of the formation of the deposits as well as the deposits’ architecture. A combination of mineralogical research and digital technology (GIS) was used to characterise the deposits. Rare earth elements from the cerium series were found in the following quantities: La (in ppm), 43–200; Ce, 57–206; Sm, 100–300; Eu, 22–100. Yttrium-series elements were found in the following quantities: Y, 31–106; Gd, 100–200; Tb, 100–200; Dy, 0–300; Ho, 0–20; Er, 0–364; Tm, 0.28–0.85; Yb, 2.2–39; Lu, 0–200. The wireframe and block models indicated that the bodies’ forms were 1800 m wide, 3500 m long, and 20–40 m thick. The major REE group minerals in both bodies were monazite and xenotime, whereas the minor minerals included yttrium parisite, silicorabdophanite, thorite, and orangite; moreover, ilmenite and titanomagnetite were found. The 3D models that were constructed indicated that the mineralogy and geochemistry of the ore bodies played a determining role in the deposits’ architecture. Full article

The ion-adsorption rare earth deposit developed on the Mosuoying granite in the Panxi area of southwestern China represents a significant advancement in the exploration of ion-adsorption rare earth deposits in Sichuan. Being the first and currently the sole ion-adsorption rare earth deposit in Sichuan, studying its rare earth mineralization characteristics holds great importance. This paper aims to investigate the geochemical properties of the Mosuoying granite and its overlying weathered crust using rock geochemical methods based on field geological investigations. The findings reveal that the deposit belongs to the light rare earth type, with the ore-forming parent rock attributed to the high-potassium calc-alkaline series. It exhibits a high rock REE content ranging from 419 to 578 ppm, indicating favorable mineralization potential. Hydrothermal alteration reduces the REE content of the parent rock, leading to a notable increase in the LREE/HREE ratio, thus impacting the partitioning of rare earth elements and subsequent ore formation. The distribution characteristics of rare earth elements in each layer of the weathered crust are controlled by the parent rock and exhibit a light rare earth distribution pattern. The completely weathered layer is the main enrichment zone for rare earth elements, and the migration and enrichment patterns of rare earth elements in the weathered crust are evident. From the semi-weathered layer to the completely weathered layer, all REEs were gained, with a higher degree of migration for LREE. From the completely weathered layer to the clay layer, all REEs were lost, and the vertical distribution of rare earth content shows a “low-high-low” pattern. Full article

Granites are assumed to be the main source of heavy rare-earth elements (HREEs), which have important applications in modern society. However, the geochemical and petrographic characteristics of such granites need to be further constrained, especially as most granitic HREE deposits have undergone heavy weathering. The LC batholith comprises both fresh granite and ion-adsorption-type HREE deposits, and contains four main iRee (ion-adsorption-type REE) deposits: the Quannei (QN), Shangyun (SY), Mengwang (MW), and Menghai (MH) deposits, which provide an opportunity to elucidate these characteristics The four deposits exhibit light REE (LREE) enrichment, and the QN deposit is also enriched in HREEs. The QN and MH deposits were chosen for study of their petrology, mineralogy, geochemistry, and geochronology to improve our understanding of the formation of iRee deposits. The host rock of the QN and MH deposits is granite that includes REE accessory minerals, with monazite, xenotime, and allanite occurring as euhedral inclusions in feldspar and biotite, and thorite, fluorite(–Y), and REE fluorcarbonate occurring as anhedral filling in cavities in quartz and feldspar. Zircon U–Pb dating analysis of the QN (217.8 ± 1.7 Ma, MSWD = 1.06; and 220.3 ± 1.2 Ma, MSWD = 0.71) and MH (232.2 ± 1.7 Ma, MSWD = 0.58) granites indicates they formed in Late Triassic, with this being the upper limit of the REE-mineral formation age. The host rock of the QN and MH iRee deposits is similar to most LC granites, with high A/CNK ratios (>1.1) and strongly peraluminous characteristics similar to S-type granites. The LC granites (including the QN and MH granites) have strongly fractionated REE patterns (LREE/HREE = 1.89–11.97), negative Eu anomalies (Eu/Eu* = 0.06–0.25), and are depleted in Nb, Zr, Hf, P, Ba, and Sr. They have high ⁸⁷Sr/⁸⁶Sr ratios (0.710194–0.751763) and low ¹⁴³Nd/¹⁴⁴Nd ratios (0.511709–0.511975), with initial Sr and Nd isotopic compositions of (⁸⁷Sr/⁸⁶Sr)_i = 0.72057–0.72129 and εNd(220 Ma) = −9.57 to −9.75. Their initial Pb isotopic ratios are: ²⁰⁶Pb/²⁰⁴Pb = 18.988–19.711; ²⁰⁸Pb/²⁰⁴Pb = 39.713–40.216; and ²⁰⁷Pb/²⁰⁴Pb = 15.799–15.863. The Sr–Nd–Pb isotopic data and T_DM2 ages suggest that the LC granitic magma had a predominantly crustal source. The REE minerals are important features of these deposits, with feldspars and micas altering to clay minerals containing Ree³⁺ (exchangeable REE), whose concentration is influenced by the intensity of weathering; the stronger the chemical weathering, the more REE minerals are dissolved. Secondary mineralization is also a decisive factor for Ree³⁺ enrichment. Stable geology within a narrow altitudinal range of 300–600 m enhances Ree³⁺ retention. Full article

The critical metal contents of four types of seabed mineral resources, including a deep-sea sediment deposit, are evaluated as potential rare earth element (REE) resources. The deep-sea resources have relatively low total rare earth oxide (TREO) contents, a narrow range of TREO grades (0.049–0.185%), and show characteristics that are consistent with those of land-based ion adsorption REE deposits. The relative REO distributions of the deep-seabed resources are also consistent with those of ion adsorption REE deposits on land. REEs that are not part of a crystal lattice of host minerals within deep-sea mineral deposits are favorable for mining, as there is no requirement for crushing and/or pulverizing during ore processing. Furthermore, low concentrations of Th and U reduce the risk of adverse environmental impacts. Despite the low TREO grades of the deep-seabed mineral deposits, a significant TREO yield from polymetallic nodules and REE-bearing deep-sea sediments from the Korean tenements has been estimated (1 Mt and 8 Mt, respectively). Compared with land-based REE deposits, deep-sea mineral deposits can be considered as low-grade mineral deposits with a large tonnage. The REEs and critical metals from deep-sea mineral deposits are important by-products and co-products of the main commodities (e.g., Co and Ni), and may increase the economic feasibility of their extraction. Full article