REE Contents Research Articles

Secondary Deposits as a Potential REEs Source in South-Eastern Europe

The main objective of this manuscript is to collect, classify, and compile all available data about secondary mineral sources of REEs in the South-Eastern Europe (SEE). The material is generated from the extracting and processing sector, that might be possibly transformed in the business process becoming an important raw material for another industry. The management inventory guide will strengthen communication and dissemination efforts and simultaneously contribute to Europe’s self-sufficiency and support transitioning to green and digital technology. Identification of the knowledge gaps associated with secondary sources of REEs in SEE will contribute to connections between all partners being involved at the beginning, during the lifetime of products and at the end of the life cycle, represented with deposit owners, technology developers and potential processors, producers, and potential users. At the investigated area it was found 1835 individual landfills, most of them belonging to waste rocks. The total quantity of all material in SRM is about 3.2 billion tons on an area of about 100 km2. The largest 95 individual landfills were selected as potential prospective landfills, containing about 1600 million tons of material. The estimated total potential of REEs (ΣREE) is more than 200 Kt. The largest quantities are found in landfills for coal fly ash and Cu flotation, which correspond to more than 80% of the ΣREE. Most of the promising sites are located in Serbia and North Macedonia. It has been calculated that the valorisation potential and perspectivity of REE2O3 is about 32.5 billion USD (prices from December 2022). According to the average concentrations of REEs, the most prospective are the red mud dams but their total volume is limited compared to massive amounts of coal fly ash landfills. The REEs content in all type of investigated materials, especially in coal fly ash in North Macedonia is twice as high as in other countries.

Detail mineralogical study and geochronological framework of Bayan Obo (China) Nb mineralization recorded by in situ U-Pb dating of columbite

The Bayan Obo deposit is world-famous for its giant rare earth reserves, and also accompanied with 2.2 Mt Nb2O5 resources at an average grade of 0.13 %, renowned as the second largest Nb deposit globally. Previous studies have focused on the origin of carbonatite (igneous/sedimentary), and variation composition during evolution, as well as its super-enrichment of light rare earth elements (LREE), while the metallogenic mechanism of niobium is being overlooked despite the identification of plenty Nb-bearing minerals. In this study, we identify four types of columbite as major Nb-bearing minerals, instead of pyrochlore in the west pit of Bayan Obo. Detailed mineralogical study has revealed large primitive columbite (Clb1-I, 100–200 μm) is hosted in the coarse-grained Fe-dolomite carbonatite (FeO = 5.46–10.47 wt%), being an ideal target for future mineral beneficiation. Those columbites (Clb1-I) are featured by lowest Sr, Y, and ∑REE but enriched in iron in composition, revealing its magmatic origin. Sieve-textured columbite (Clb1-II, ∼100 μm) dispersed in the fluorination and chloritization dolomite carbonatite, with a U–Pb age of 1359 ± 31 Ma, contemporary with ages of the regional carbonatite magma intrusion and rift-related magmatism, indicating niobium being sourced from mantle-derived carbonatite. The occurrence of fluorite as inclusions in Clb1-I indicates the solubility of Nb was enhanced by fluxes, and the columbite saturation was easily achieved during the carbonatite magma evolution into ferroan carbonatite. Strong fenitization metasomatism further locally concentrated columbite either within the mineral assemblages of pyrite + phlogopite + allanite (Clb2) or in the mica-dominated fenite (Clb3), and crystallized at 346 ± 18 Ma and 284 ± 16 Ma, respectively. The latter metalogenetic epoch is accordant with late Permian granitic magmatism event (ca. 280 Ma) while the former age may attribute to its occurrences related to the early Paleozoic arc-continent collision. Differ from pristine columbite (Clb1-I and Clb1-II), the metamorphic columbite (Clb2 and Cl3, especially Clb3) are enriched in Ta (1803–4092 ppm), Y (560–2029 ppm) and ∑REE (720–6317 ppm) content, probably suggesting the highest degree of evolution. The similar metallogenesis framework between Nb and REE, combined with the coexistence of columbite and REE minerals assemblages, implies the spatial and temporal coupling of Nb and REE mineralization. This first innovative and systematic mineralogical and geochronological work directly constrains the nature of Mesoproterozoic mantle-derived carbonatite with fertile Fe and fluxes, and the Paleozoic and Permian fenitization metasomatism, are the major factors contribute to the metallogenic specialization of niobium in Bayan Obo.

REEs Prospects in Laterites Profiles of Ibra, Sultanate of Oman

REEs now days are acting as an alternative source of low- sustainable energy economy and got strategic significance in the development of most of the current high-end technologies in industries and Laterite deposits provide one of the major natural sources of REEs. Laterite soil or rock is a product of intensive and prolonged weathering of underlying parent rock formed in hot and wet tropical areas. It is mainly rich in iron and aluminum oxides. The development of laterite profiles in most of Oman Mountains is mainly related to the late Cretaceous (Coniacian to late Companion) tectonic evolution of the Oman Mountains which are part of the Alpine–Himalayan fold belt. Laterite and regolith formations can be found overlie the Samail ophiolite in Oman. Samail Ophiolite is a part of upper mantle & Oceanic lithosphere which over thrusted on to the continental crust. The Samail ophiolite is considered as one of the major features of the Oman Mountains. The present study focuses on the REEs prospects in the Ibra region of Sultanate of Oman and study area of Ibra region lies within the Samail Ophiolite. The fieldwork was carried out for geological evaluation at the Ibra region. Total 3 number of Laterite profiles were observed during the fieldwork. Samples were collected from the Harzburgite rock. All samples were analyzed for ICPMS analysis to know the REEs. Field observation and chemical analysis clearly indicates that the Ibra region might have good prospect for REEs exploration and mining based on their REEs content

Accurate determination of ultra-trace rare earth elements by LA-ICP-MS/MS and its application to cassiterite for effective elimination of Gd and Tb false positive anomalies

This study reports a new method for in situ determination of ultra-low REE contents in cassiterite by LA-ICP-MS/MS with an O2 and mass-shift detection strategy to avoid Gd and Tb anomalies.

LREE rich perovskite in antiskarn reactions - REE transfer from pyroxenites to carbonatites?

We study three ultrabasic-alkaline carbonatite complexes (UACCs: Afrikanda, Vuorijarvi, Kovdor) from the Kola Alkaline Province to focus on the comparison of REE contents from pyroxenites and carbonatites and the fate of perovskite. Pyroxenites and carbonatites have large REE variations and similar contents in all three complexes. Afrikanda and Vuorijarvi pyroxenites and carbonatites have higher REE contents compared to all Kovdor rocks. Despite their comparable LREE contents, pyroxenites and carbonatites have different REE-carrier minerals. In most studied pyroxenites, perovskite is the main REE-bearing mineral and its abundance controls the LREE enrichment of the whole rock. When perovskite is absent or in low abundance, apatite is the main REE carrier. Instead, in carbonatites and phoscorites, apatite and calcite control REE contents. REE‑carbonates - found in several carbonatite samples - do not play a substantial role in the overall REE budget because of their very low abundance and tiny grain sizes.We found large LREE variations at very low local scales (< 1 mm) in several thin sections. These large variations are related to carbonatite infiltration and associated antiskarn reactions. Perovskite near calcite is replaced by titanite that has much lower LREE contents. Most LREE released from the breakdown of perovskite were probably dissolved in the carbonatite melt because apatite and calcite that crystallized from this melt are highly enriched in LREE. Newly formed apatites and calcites show large LREE variations that probably are controlled by local factors (e.g. variations of Si, Ca, Mg activities). Y/Ho ratios are strongly fractionated in most minerals and often show large variations at local scales (mm) in these antiskarn reactions. The potential of REE remobilization from such perovskite replacement reactions is very high as perovskite contributes about 70% to the REE budget for these three UACCs. Therefore, more attention should be given to perovskite replacement reactions and its role for LREE enrichment of carbonatite melts.

Mineralogical constraints on pegmatite genesis and rare metal mineralization in the Mufushan batholith, South China

Pegmatites are commonly associated with or strongly influenced by the crystallization of magmatic volatile phases (MVP) as ascending magmas undergo differentiation. The mechanism of fractional crystallization, liquid immiscibility, and water–rock interactions that influence the rare metals concentration in pegmatites are still unclear. We analyzed the mineralogy (incl. monazite, garnet, zircon, and muscovite) from pegmatites to unravel the timing and magmatic-hydrothermal processes for the giant Renli-Chuanziyuan pegmatite Li-Nb-Ta mineralization in the Mufushan region (South China). Five types of pegmatites have been identified at Mufushan, i.e., those containing mainly orthoclase (O-pegmatite), microcline (M-pegmatite), albite-orthoclase (AO-pegmatite), microcline-albite (MA-pegmatite), and spodumene-albite (S-pegmatite).Monazites from the Renli high-Th Li-mica pegmatite exhibit magmatic affinity. The ∼140 Ma age of monazite U-Pb suggests a temporal relationship between the Li-rich pegmatite and its muscovite granite host. Garnet from these pegmatites is magmatic and belongs to the almandine-spessartite series, and contains feldspar and apatite inclusions. Continuous fractional crystallization likely controlled the pegmatite development, as the garnet spessartite content increases with distance from the Mufushan batholith. Garnet in the spodumene-albite pegmatites has very low REE content, and it represents a late stage of crystallization related to magmatic-hydrothermal fluids. Compositional variation in muscovite from all of the pegmatites is negligible. The K/Rb ratio (a proxy for the degree of fractionation) increases gradually from the O- to S-pegmatite, whilst the muscovite F content correlates positively with the degree of magma fractionation. The transformation of muscovite to lepidolite in pegmatites can occur through magmatic-hydrothermal crystallization or metasomatism. Zircon in pegmatites generally occurs as metasomatic remnants, with uneven zoning shown in cathodoluminescence (CL) images. Hydrothermal zircon U-Pb ages are concentrated in the 140–134 Ma range, consistent with the garnet leucogranite ages. This suggests that pegamtites and the garnet leucogranite were formed in the same magmatic-hydrothermal activity. The accumulated MVP and incompatible elements may have migrated from deeper, more crystal-rich zones under medium degree of fractionation. The MVP may contain abundant dissolved melt components as single-phase hydrous silicate liquids, forming typical quartz-/feldspar-dominated pegmatite and the diversity of rare-metal deposits.

Metallurgical Properties of CeLa Substituted Bio-Glass Ceramics

To set up a bioglass of general structure given in Table 1. These five samples were ready in a crucible made up of alumina through a melting temperature of 1400±10 oC and normalized it. The glass powder pallet was made by the press and submerged in Simulated Body Liquid (SBF) in various time spans, and they’re not entirely settled by FTIR examination. The morphology of the surface resolved to utilize a Checking by (SEM). pH estimation of bioactive glass was done by pH meter and mechanical properties like Microhardness and Flexural strength were determined and found that it increases with increasing the concentration of REEs. The developed CeO2 and La2O3 incorporated bioactive glasses were also found to enhance mechanical properties. Thus, the glasses with CeO2 and La2O3 can be suitable candidates for bone implant application.

The Raman spectrum of florencite‐(REE) [REEAl3(PO4)2(OH)6]: An integrated experimental and computational approach

AbstractFlorencite is a hydrous light rare‐earth elements (LREE) aluminium phosphate [REEAl3(PO4)2(OH)6], that amongst the REE‐rich minerals is quite common. The main end‐members are Ce‐, La‐ and Nd‐rich terms that were found in several genetic environments. Despite the large occurrence worldwide, to the authors' knowledge, florencite has attracted very few studies, particularly concerning the characterization of its Raman spectrum. We present a detailed study of the Raman spectrum of florencite, combining experimental measurements and theoretical calculations. Experimental Raman spectra (in the 100–1300 cm−1 spectral range) are measured on four florencite samples characterized by different chemical composition, that is, different REE abundance. The results highlight a remarkable coincidence between different Raman spectra measured on each sample, despite the significantly different chemical compositions in terms of their REE content. The same similarities were also observed in the computed spectra at the ab initio level; moreover, the calculations allowed the attributions of the different Raman signals to specific vibrational modes.

Characterization of complex micellar systems by Scattering techniques (SAXS and SANS) and wet-scanning transmission electron microscopy (wet-STEM)

The morphology of complex micellar assemblies is generally described using indirect methods such as small-angle X-ray scattering (SAXS) or small angle neutron scattering (SANS) that can yield to ambiguous descriptions of the nano-objects when the sample contains multiple structures or completely unknown structures. We herein propose to directly observe the nano-objects formed in P123 pluronic solutions (with and without rare-earth element - REE) using wet-Scanning Transmission Electron Microscopy (wet-STEM) and to compare the results with sample descriptions derived from SAXS and SANS measurements. The results obtained by the different analytical techniques are consistent. Each analytical method provides complementary information that allows the internal structure of the objects, their compositions and their mutual interactions to be described precisely. The main contributions of wet-STEM microscopy are to describe the nano-objects individually and, in particular, to show that the REE content can vary from 1 to 10 from one micelle to another, to observe the dynamics of the nano-objects in the liquid and to prove the co-existence of nano-objects with very different morphologies in the same system.

Apatite geochemical composition of Mesozoic granitoids in the eastern Jiangnan Orogen, S. China: insights into petrogenesis and intrinsic magmatic variables

ABSTRACT The geochemical compositions of apatite are commonly used to provide reliable constraints on the intrinsic magmatic variables of the parental magma. There is a widespread distribution of Mesozoic granitic rocks in the eastern Jiangnan Orogen (EJNO), which include I-type and A-type granitoids. This study aims to investigate the geochemical composition of apatite in 11 representative I-type and A-type granitic intrusions from the EJNO to understand their petrogenesis, intrinsic magmatic variables, and polymetallic mineralization potential. The results show that apatites in these granitoids were characterized by oscillatory zonation and homogeneous texture, and exhibited high F, and low Cl contents, as well as high REE, Y, and Th contents, indicating magmatic origin. These apatites were divided into two groups depending on their geochemical characteristics and original rock types. In Group I apatites (in the I-type granitoids), the absence of an abrupt change in major and trace element concentrations from the core to the rim of the apatite crystals, combined with their low levels of MgO, Sr, and HREY (HREE+Y), serves as evidence to classify the I-type granitoids as low Sr-Y adakitic granitoids with a low Mg#, which can be attributed to the partial melting of the thickened lower crust. In Group A apatites (in the A-type granites), the normal increase in incompatible elements from the core to the rim, as well as the presence of a flat REE pattern with pronounced Eu anomalies, can be attributed to crystal fractionation of plagioclase, allanite, and zircon. Furthermore, Group I apatites have higher SO3, Cl, and molar OH/F and Cl/F ratios compared to Group A apatites. Quantitative calculation by apatite-melt partitioning and modelling suggests that the I-type granitic magmas were more volatile-rich and more oxidized than A-type granitic magmas. Taken together, based on the relationship between the intrinsic magmatic variables and the behaviour of ore-forming elements, our study demonstrates that early I-type granitoids of the EJNO have a strong W-Mo-Cu polymetallic mineralization potential, while late A-type granites may possess rare metal mineralization potential.

Trace Elements of Multi‐stage Minerals and Titanite U‐Pb Dating for the Gneisses from Liansan Island, Sulu UHPM Belt

AbstractGneisses with anatectic characteristics from the Liansan island in the Sulu UHPM (ultra‐high pressure metamorphic) belt were studied for petrography, titanite U‐Pb dating and mineral geochemistry. Three origins of garnets are distinguished: metamorphic garnet, peritectic garnet and anatectic garnet, which are formed in the stages of peak metamorphism, retrograde anatexis and melt crystallization, respectively. The euhedral titanite has a high content of REE and high Th/U ratios, which is interpreted as indicating that it was newly‐formed from an anatectic melt. The LA‐ICP‐MS titanite U‐Pb dating yields 214–217 Ma ages for the titanite (melt) crystallization. The distribution of trace elements varies in response to the different host minerals at different stages. At the peak metamorphic stage, Y and HREE are mainly hosted by garnet, Ba and Rb by phengite, Sr, Nb, Ta, Pb, Th, U and LREE by allanite and Y, U and HREE by zircon. During partial melting, Y, Pb, Th, U and REE are released into the melt, which causes a dramatic decline of these element contents in the retrograde minerals. Finally, titanite absorbs most of the Nb, U, LREE and HREE from the melt. Therefore, the different stages of metamorphism have different mineral assemblages, which host different trace elements.

Geochronological Constraints on the Evolution and Petrogenesis of the Malwa Plateau Subprovince of the Deccan Traps

AbstractThe eruptive history of the Malwa Plateau Subprovince of the Deccan Traps is addressed by dating 21 lavas spanning the exposed stratigraphic extent, using the 40Ar/39Ar method applied to plagioclase separates. Major, minor, and trace element geochemistry was determined for each of the dated lavas and four additional ones. Dating results indicate that the eruptions began prior to 66.8 Ma, at least 400 ka before the oldest known lava in the more extensively studied Western Ghats, representative of the main Deccan province, to the south. Eruption rates peaked from 66.4 to 66.3 Ma and then diminished until 65.6 Ma. The peak in eruption rates coincides with the well‐documented Late Maastrichtian Warming event. Malwa lavas show some major and trace element affinities with geochemically defined lava flow formations of the Western Ghats, but are generally out of the stratigraphic sequence manifest in the Western Ghats. The distinct geochemical evolution of Malwa Plateau lavas compared with those of the Western Ghats is at least in part a consequence of differences in crustal composition between the two subprovinces. Modeling of REE concentration patterns of Malwa lavas suggests that they were derived by slightly lower degrees of partial melting, at lower mantle temperatures and depths, than those in the Western Ghats. The Malwa Plateau thus appears to record an earlier, cooler stage of the Deccan plume's evolution and continued to erupt through a large part of the lifetime of the main Deccan province.

Ecological and geochemical assessment of soil cover on the territory of Ufa city

The relevance. The need for constant monitoring of the state of natural environments because of Ufa increasing industrialization. This study is especially relevant due to the presence of enterprises of various industries (petrochemical, energy, metal construction, timber processing, chemical) located on a fairly small territory of the millionaire city. The aim. To determine the degree of technogenic pollution of the soil cover from industrial facilities in the study area. It is necessary to assess the impact of industrial emissions, as well as emissions from stationary and mobile sources for development of measures aimed at reducing the impact of chemical elements on the environment. Methods. Instrumental neutron activation analysis, atomic absorption spectroscopy, kappametry, mathematical statistics, mapping (spatial distribution of indicator geochemical indicators and content of the main pollutants). Results. The paper introduces the results of the analysis of the content of 29 chemical elements in the soil cover on the territory of Ufa according to the study of 104 samples. For each industrial area of the city, the priority elements-pollutants from the list of the analyzed ones were identified. Areas with high traffic congestion, as well as areas near oil refineries, are characterized by increased concentrations of As and LREE group (La, Ce, Nd). Elevated levels of Br and Sc are observed in areas near energy complexes. Increased concentrations of REE (Nd, Tb, Lu) were detected around the objects of the timber industry complex. A special situation is observed with the concentrations of some metals (Cr, Zn, Co). The entire territory of the city is characterized by increased concentrations of elements of the transition metal group due to the presence of a large metalworking complex and heavy automobile traffic. Using statistical methods of data interpretation, associations of chemical elements were identified and divided by possible genesis: mainly natural (Ca-Sr), mixed (Cs-Rb, Br-Ta-Na), mainly technogenic (Sb-Zn, Ba-As-Cr-Hg, Th-Lu-Hf-Yb, Ce-La-Nd). The constructed maps-schemes of spatial distribution, the total indicator of pollution and magnetic susceptibility determined that the territory of Ordzhonikidze district and the territory of the Dema railway station can be considered as the most susceptible to anthropogenic influence.

Tracing provenance of eolian sands in the northern Ulan Buh Desert, China: Evidence from the REE geochemical characteristics

Desertification is a primary threat to crop farming, the livestock industry, and the eco-environment in northwestern China. Through field research and satellite imagery, it has been discovered that there are 4–5 sand belts in the shape of handclasps connecting major deserts in the Alxa Plateau region of northern China. These sand belts have been expanding for several decades. However, eolian sand transport between major deserts through these expanding sand belts is still underestimated. Identifying the source areas of eolian sands in deserts provide essential knowledge to prevent desertification. In this study, we collected samples from the northern Ulan Buh Desert (UBD), the Yamalik Desert (YD), and the Langshan Mountains and analyzed their REE contents in the <125 μm fraction. We compared REE geochemical characteristics of fine-grained sands in the UBD with other recently published REE data for potential source areas. Our findings indicate that the primary origins of fine-grained sands in the northern UBD are from the Qilian Mountains (QM) and Badain Jaran Desert (BJD), which are transported through the YD. Contributions from the Gobi-Altay Mountains to the north are relatively minor. The Langshan Mountains and Hawula Mountains are not considered as the primary sources of fine-grained sands in the UBD. In contrast, surface sediments in the southern UBD have a local mixture of the paleo-lacustrine deposits, the Gobi sediments, and minor external inputs from the BJD and QM. Our findings demonstrate that sand belts connecting these deserts play a crucial role in the eolian transport of fine-grained sands. Therefore, both the Chinese government and scientists should pay close attention to them in future efforts to combat desertification.

Geochemical characteristics and implications of epidote in South Dulan and Vlaska exploration greenfield in north of Bor metallogenic zone, Serbia

The Bor metallogenic belt in Serbia is a promising region for copper-gold (Cu-Au) resources, hosting numerous porphyry copper deposits, epithermal gold deposits and metallogenic prospects, such as the South Dulan and Vlaska exploration greenfield. Epidote alteration is integral to the propylitic and sodic-calcic alteration assemblages within this region. It is distinguished by the extensive occurrence of two primary epidote types: disseminated (Ep1) and veined (Ep2) epidote. In this study, comprehensive petrographic analysis reveals that in the propylitic zone, epidote mainly replaced hornblende (Ep1a) and plagioclase phenocrysts (Ep1b), coexisting with chlorite, apatite and titanite. In proximity to the potassic zone, epidote (E1c) coexists with biotite, while epidote (Ep2), chlorite, pyrite and chalcopyrite veinlets are observed near the ore body. Notably, Ep1 exhibits lower Fe and higher Mn contents in comparison to Ep2. Additionally, elements such as Ca, Al and Fe in Ep1a, and Ca, Fe, Mg, Mn and Ti in Ep1b, as well as Ca, Al, Fe and Mn in Ep1c, are introduced into the epidote through hydrothermal fluid interactions. Variations in trace element characteristics are evident among different epidotes. Specifically, Ep1a exhibits elevated Mg content (324–6050 ppm), Ep1b is notable for its high Na (22–942 ppm) and Sr (523–3075 ppm) contents, while Ep1c contains elevated K (24–445 ppm) and Na (41–103 ppm). Which suggest that disseminated epidote (Ep1) inherits the geochemical features from its precursor minerals. In comparison to disseminated epidote, epidote in veinlet exhibits higher Fe3+, Cu, Sn and REEs, along with lower contents of Pb, Sb and Sc, suggesting that these elements have been integrated into epidote through isomorphism substitution and influenced by fluids compositions, physical factors (temperature, pressure, etc.) and chemical parameters (speciation, pH, fO2, etc.), as well as mineral assemblages. Therefore, the trace element contents of Pb, Sb, Sc, Cu, Sn and REEs in epidote could serve as more appropriate indicators for mineral geochemistry in porphyry deposit hydrothermal centers.

Petrogenesis and rare-metal mineralization of the Ririwai alkaline granitoids, north-central Nigeria: mineralogical and geochemical constraints

ABSTRACT The Ririwai anorogenic alkaline complex harbours extensive rare metal (Nb-Zr-Sn-Zn) mineralization. However, uncertainty still surrounds their origin and magmatic-hydrothermal processes responsible for their rare metal mineralization. The complex is composed of peralkaline arfvedsonite ± albite-bearing granites, mildly peralkaline fayalite-bearing granite porphyries, and weakly peraluminous biotite-bearing granites, all of which show diagnostic A1-type characteristics. Zircon U-Pb dating reveals emplacement ages between 181.4 ± 0.81 and 188.6 ± 7 Ma for the three rock units. Sm-Nd and Pb isotopes (εNd (t) = –0.6 to −5.4, 206Pb/204Pb = 17.68–17.93) constrained the Ririwai A-type granites to represent highly fractionated products of enriched mantle-derived magmas. Mass-balance modelling suggests that magma evolution was fuelled by extensive fractional crystallization of 50 ~ 60 vol.% K-feldspar, 30 ~ 35 vol% fayalite, 5 ~ 10 vol.% amphibole, and ~ 5 vol.% apatite under reduced and water-undersaturated (ΔFMQ = –1.55; logfo2 = –18.63; H2O = <2.0 wt.%) conditions and assimilation of ~ 50 vol.% crust. Whole rock and amphibole compositions revealed an increasing degree of fractionation from the fayalite-bearing granite porphyries through biotite-bearing granites to the arfvedsonite ± albite-bearing granites. This extended fractionation at the late stage of magma differentiation, facilitated by fluorine dissolution and concentration of excess HFSE and REE as alkali-fluorocomplexes in the fluorine-rich silicate melt, allowed the accumulation of economic rare metal pyrochlore and columbite mineralizations in the highly fractionated arfvedsonite± albite- and biotite-bearing granites, respectively. Nonetheless, the metasomatic reaction rim textures around the magmatic pyrochlore, coupled with the M-type lanthanide tetrad effect (TE1,3 >1.10) indicate the subsequent effect of hydrothermal processes. Tectonically, reactivated shear fractures and transcurrent faults following lithospheric stresses in a transtensional regime allowed magma uprising and emplacement of A-type granites in the Ririwai complex.

Cathodoluminescence and geochemical characteristics of Apatite: Implications for mineral exploration in the Xiongcun District, Tibet, China

Apatite grains from the No. 2 porphyry Cu–Au deposit in the Xiongcun district of Tibet, China, have a range of physical and compositional features. This study investigates the potential use of apatite associated with hydrothermal alteration as a tool for mineral exploration. In situ textural, cathodoluminescence (CL), and chemical analyses were performed on thin sections containing apatite from various alteration zones in the deposit. No clear variation was seen in apatite from rocks of the potassic, sodic–calcic, chlorite–sericite, phyllic, and propylitic alteration zones using visible light and scanning electron microscopy; however, distinct variations were observed in optical cathodoluminescence (OP-CL) (dark yellow to green, orange to green, yellow–brown to green, yellow-orange to brown, and light yellow–brown to green luminescence for the respective zones). The alteration-related differences in luminescence were a result of the interaction between Fe and Mn; the Na and Cl contents; and depletion in total heavy rare earth elements (ΣHREE) and Y. The variations in the REE contents of apatite from different types of altered rock record reactions with Cl- and F-rich fluids. The partitioning behavior of Cl between apatite and hydrothermal fluids is influenced by pressure, temperature, pH, and fluid composition, whereas the partitioning of F between apatite and fluids is dependent on the fluid composition and not the temperature. At high temperatures, Eu3+ is reduced to Eu2+, which results in negative Eu anomalies in apatite from the potassic-altered rocks and propylitic-altered rocks. Apatite grains in the sodic–calcic-altered rocks and chlorite–sericite-altered rocks show a similar enrichment in light REEs (LREEs) that resulted from REE and Y incorporation as follows: Na+ + (Y + REE)3+ = 2Ca2+. Apatite grains in the phyllic-altered rocks are enriched in the middle REEs. This study confirms that the luminescence, chemical composition (including Fe, Mn, Na, Cl, ΣHREE, and Y contents), and REE patterns of apatite can be affected by hydrothermal alteration; therefore, these results may be used to constrain the evolution of ore-forming hydrothermal fluids and may offer an effective tool for mineral exploration.

Geochemical and Mineralogical Characteristics of Ion-Adsorption Type REE Mineralization in the Mosuoying Granite, Panxi Area, Southwest China

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.

Geochemistry of the Leatherwood coal in eastern Kentucky with an emphasis on enrichment and modes of occurrence of rare earth elements

The Middle Pennsylvanian (Bolsovian) Leatherwood coal in the central part of eastern Kentucky is a moderately thick, moderate-S seam that has been one of the major energy resources in the region. Much of the seam profile consists of clarain, dull clarain, and durain with some brighter lithologies at the base of the seam and in the upper portion of the coal at one site. A previous study emphasized petrographic trends. In this investigation, the geochemistry of the coal is examined. Some elements, such as Ge and Ga, are enriched at 2× and 5× the World hard coal averages in the coal lithotypes adjacent to rock (roof, floor, partings). Arsenic and other chalcophile elements (Zn, Co, Ni) tend to be concentrated at the top and bottom of the seam profiles and below partings, generally in the coals with the highest pyritic sulfur content. Manganese enrichments occur in bright clarain lithologies at one site. No coal lithology reaches a 5× the World hard coal average, but samples between the 2× and 5× World hard coal averages tend to be at the top and bottom of the coal seam. Most coal samples tend to have a light rare earth element (LREE) enrichment. The basal lithotype at all sites, though, has a heavy REE enrichment and, via inference from the Zr and TiO2 concentrations, a smaller influx of detrital minerals than the basal lithotypes in many Appalachian coals. While the nature of REE associations is complicated by the high volatile A bituminous coal rank, the relatively high concentrations of the heavy REE suggest an original, albeit possibly not exclusive, organic association for those elements.

Geochemical characteristics and ecological risks of rare earth elements in river sediments of coal-grain composite area in eastern China.

Coal and grain complex areas influence the geochemical characterization of REEs through coal mining activities and agricultural production. However, there is a lack of relevant studies. In this study, we investigated the geochemical characterization and risk assessment of REEs in river sediments of the northern Anhui plain, a typical coal-grain composite area. The results showed that the average concentrations of ∑REE in the sediments ranged from 134.7 to 220.3 μg/g, and LREE was significantly enriched. Among the 14 REEs, Gd and Eu were the most enriched, with enrichment factors of 1.792 and 1.764, respectively. In addition, the differences in REEs content and enrichment between different rivers were related to the location of coal mines and the degree of population concentration. The average values of δCe and δEu in the sediments were 0.990 and 1.080, respectively, and most of the sampling sites showed a weak positive Ce, Eu anomaly. The results of Pearson's correlation and RDA redundancy analyses showed that Fe, Al, Mn and sand contributed more to the enrichment of REEs. The river sediments in the whole area had a slight potential ecological risk, with Eu (Er=13.05) and Lu (Er=14.07) having the highest potential risk. The ADD results also showed that the average daily dose of REEs by children was around 2.000 (μg/(kg·day)), which was significantly higher than that of adults. The results of this study can be used as a basis for the prevention and control of REEs in rivers in northern Anhui Province.