Search Results (34)

Zircon is one of the most common accessory minerals in all types of granitoids. Due to its resistance to secondary processes, it preserves information about the composition of magma and conditions at the time of crystallization. Madeira albite granite, Brazil, offers optimum conditions for the study of chemistry and shape of zircon and the relation between the contents of particular trace elements in magma vs. in crystallizing zircon. Textural and chemical zircon data obtained using scanning electron microscopy (BSE) and cathodoluminescence (CL) imaging, automated mineralogy by TESCAN Integrated Mineral Analyzer (TIMA), and electron probe microanalyses (EPMA) enabled us to define four albite granite facies containing zircons of specific structures and chemistry. Zircon in the Madeira albite granite was formed during several, largely temporally and spatially independent episodes. During the crystallization of the common facies, occupying most of the intrusion volume, Zr/Hf value in zircon decreased from 40 to 20. This zircon, in some episodes, incorporated a higher amount of Th, which was later unmixed in the form of thorite inclusions. The pegmatoidal facies, representing crystallization of residual magma, contains zircon without thorite inclusions with a Zr/Hf value from 35 to 5. The Th/U and Y/Yb values during this evolution scattered but generally evolved to Th, Yb-enriched compositions (Th/U up to >10, Y/Yb down to 0.1). The Li-poor facies, located in the center of the stock near the cryolite deposit, contains zircon with comparatively high Zr/Hf = 45–70 and higher U and Y contents. Later, part of the common facies was hydrothermally altered to border facies, but zircon did not change noticeably during this process. The contents of minor elements in all zircon varieties are generally low (U + Th + Y + REE ˂ 0.05 apfu); Y and REE are incorporated exclusively in the xenotime component. Many crystals have low analytical totals, down to 95 wt%, and are enriched in Al, Fe, Mn, Ca, and F but this process does not influence the primary Zr/Hf, Th/U, and Y/Yb ratios. Zircons from other Madeira granite facies, including the neighboring Europa pluton, differ mainly in much higher Y/Yb values and in having (Y + REE) >> P, indicating a different than xenotime substitution mechanism. Zircon from the Madeira albite granite differs from zircons from many metaluminous rare-metal granites in low contents of minor elements and a common assemblage with thorite, instead of forming Zrn–Thr–Xnt solid solutions. Full article

This study investigates pegmatites with exceptionally rare mineralogical and chemical signatures, hosted by the 1.8 Ga peralkaline albite-enriched granite, which corresponds to the renowned Madeira Sn-Nb-Ta-F (REE, Th, U) deposit in Pitinga, Brazil. Four distinct pegmatite types are identified: border pegmatites, pegmatitic albite-enriched granite, miarolitic pegmatite, and pegmatite veins. The host rock itself has served as the source for the fluids that gave rise to all these pegmatites. Their mineral assemblages mirror the rare-metal-rich paragenesis of the host rock, including pyrochlore, cassiterite, riebeckite, polylithionite, zircon, thorite, xenotime, gagarinite-(Y), genthelvite, and cryolite. These pegmatites formed at the same crustal level as the host granite and record a progressive magmatic–hydrothermal evolution driven by various physicochemical processes, including tectonic decompressing, extreme fractionation, melt–melt immiscibility, and internal fluid exsolution. Border pegmatites crystallized early from a F-poor, K-Ca-Sr-Zr-Y-HREE-rich fluid exsolved during solidification of the pluton’s border and were emplaced in contraction fractures between the pluton and country rocks. Continued crystallization toward the pluton’s core produced a highly fractionated melt enriched in Sn, Nb, Ta, Rb, HREE, U, Th, and other HFSE, forming pegmatitic albite-enriched granite within centimetric fractures. A subsequent pressure quench—likely induced by reverse faulting—triggered the separation of a supercritical melt, further enriched in rare metals, which migrated into fractures and cavities to form amphibole-rich pegmatite veins and miarolitic pegmatites. A key process in this evolution was melt–melt immiscibility, which led to the partitioning of alkalis between two phases: a K-F-rich aluminosilicate melt (low in H₂O), enriched in Y, Li, Be, and Zn; and a Na-F-rich aqueous melt (low in SiO₂). These immiscible melts crystallized polylithionite-rich and cryolite-rich pegmatite veins, respectively. The magmatic–hydrothermal transition occurred independently in each pegmatite body upon H₂O saturation, with the hydrothermal fluid composition controlled by the local degree of melt fractionation. These highly F-rich exsolved fluids caused intense autometasomatic alteration and secondary mineralization. The exceptional F content (up to 35 wt.% F in pegmatite veins), played a central role in concentrating strategic and critical metals such as Nb, Ta, REEs (notably HREE), Li, and Be. These findings establish the Madeira system as a reference for rare-metal magmatic–hydrothermal evolution in peralkaline granites. Full article

The current work records for the first time the rare-metal pegmatites with mixed NYF-LCT located at Wadi Sikait, south Eastern Desert of the Egyptian Nubian Shield. Most of the Sikait pegmatites are associated with sheared granite and are surrounded by an alteration zone cross-cutting through greisen bodies. Sikait pegmatites show zoned and complex types, where the outer wall zones are highly mineralized (Nb, Ta, Y, Th, Hf, REE, U) than the barren cores. They consist essentially of K-feldspar, quartz, micas (muscovite, lepidolite, and zinnwaldite), and less albite. They contain a wide range of accessory minerals, including garnet, columbite, fergusonite-(Y), cassiterite, allanite, monazite, bastnaesite (Y, Ce, Nd), thorite, zircon, beryl, topaz, apatite, and Fe-Ti oxides. In the present work, the discovery of Li-bearing minerals for the first time in the Wadi Sikait pegmatite is highly significant. Sikait pegmatites are highly mineralized and yield higher maximum concentrations of several metals than the associated sheared granite. They are strongly enriched in Li (900–1791 ppm), Nb (1181–1771 ppm), Ta (138–191 ppm), Y (626–998 ppm), Hf (201–303 ppm), Th (413–685 ppm), Zr (2592–4429 ppm), U (224–699 ppm), and ∑REE (830–1711 ppm). The pegmatites and associated sheared granite represent highly differentiated peraluminous rocks that are typical of post-collisional rare-metal bearing granites. They show parallel chondrite-normalized REE patterns, enriched in HREE relative to LREE [(La/Lu)_n = 0.04–0.12] and strongly negative Eu anomalies [(Eu/Eu*) = 0.03–0.10]. The REE patterns show an M-type tetrad effect, usually observed in granites that are strongly differentiated and ascribed to hydrothermal fluid exchange. The pegmatite has mineralogical and geochemical characteristics of the mixed NYF-LCT family and shows non-CHARAC behavior due to a hydrothermal effect. Late-stage metasomatism processes caused redistribution, concentrated on the primary rare metals, and drove the development of greisen and quartz veins along the fracture systems. The genetic relationship between the Sikait pegmatite and the surrounding sheared granite was demonstrated by the similarities in their geochemical properties. The source magmas were mostly derived from the juvenile continental crust of the Nubian Shield through partial melting and subsequently subjected to a high fractional crystallization degree. During the late hydrothermal stage, the exsolution of F-rich fluids transported some elements and locally increased their concentrations to the economic grades. The investigated pegmatite and sheared granite should be considered as a potential resource to warrant exploration for REEs and other rare metals. Full article

Molybdenite Re–Os and zircon U–Pb isotopic data are first obtained from the stockwork and disseminated-style gold-bearing ores and the fine-grained granite hosting these ores in the Xiawolong gold mine, respectively, which is located within the Muping–Rushan gold metallogenic belt, eastern Jiaodong Peninsula, so as to illustrate the genesis of gold mineralization and its implication for exploration. Four molybdenite samples yield a well-defined Re–Os isochron age of 118.4 ± 2.5 Ma (2σ), which is identical to the weighted average Re–Os model age of 118 ± 1.7 Ma (2σ). Integration of the new geochronologic data with those reported recently from the other gold mines in the Muping–Rushan gold metallogenic belt suggests that a discrete gold event occurred in Xiawolong ca. 4 m.y. older than that for the other gold mineralization at ca. 114 Ma in eastern Jiaodong. In addition, two fine-grained granite samples, measured using the LA-ICP-MS zircon U–Pb method, produce the first precise ages of 118 ± 2 to 117 ± 2 Ma (2σ), identical to the molybdenite Re–Os ages, within the margin of error and obtained in this study. The fine-grained granite has a similar lithology and emplacement age as those of the medium-grained monzogranite consisting of the marginal facies of the Sanfoshan batholith, and is considered to be the crystallization products of Sanfoshan granitic magma in the late stage. Combined with the previous S-Pb-D-O isotope, fluid inclusion and geological studies, which suggest that the ore-forming fluid of Xiawolong gold mineralization is from magmatic water, and the identification that the magnetite coexists with the gold-bearing pyrite and molybdenite in the gold ores, which indicates a high oxygen fugacity (fO₂) of both the magma and resultant hydrothermal fluids, it is logical to infer that the Xiawolong gold deposit is genetically in relation to the Sanfoshan granitic magmatism, which is high in fO₂ and rich in Au at the magmatic–hydrothermal transition stage, and the change in fO₂ mostly likely makes a significant contribution to the precipitation of Au. This result reveals that the late-stage granitic magma with high fO₂, which is crystallized into the fine-grained granite, probably is also rich in Au, except the W–Mo–Cu–Zn–U–Be–Li–Nb–Ta–Sn–Bi-elements. Therefore, based on the extensional tectonic regime for the early Cretaceous Jiaodong gold deposits, we propose that gold exploration in the Jiaodong should not only focus on the fault-hosted Au but also on the fine-grained granite-hosted Au around the apical portions of the late Early Cretaceous small-granitic intrusions with high fO₂. This model could also be important for prospecting in other gold ore districts, which have a similar tectonic setting. Full article

This study focuses on the relationship between U and pyrochlore in the world-class Sn-Nb-Ta (U, Th, REE, Li) Madeira deposit within the Pitinga mining district of northern Brazil. The primary U mineralization is of intrusive-type and early magmatic origin, hosted in the peralkaline albite-enriched granite facies of the A-type Madeira granite (~1820 Ma). U-Pb-LREE-enriched pyrochlore is the only primary U ore and is widely and homogeneously dispersed in two albite-enriched granite subfacies: the albite-enriched granite core (AGC) and the albite-enriched granite border (AGB). In both zones, the pyrochlore crystals underwent strong hydrothermal alteration by F-rich, low-temperature aqueous fluids. During this hypogene alteration process, cations such as LREE, Nb, and F were selectively released, while others like Fe and Si were introduced. This led to the successive formation of various secondary pyrochlore varieties and a relative enrichment of U (up to 13.73 wt.% UO₂). The alteration of pyrochlore eventually resulted in the breakdown of its structure, leading to the formation of U-bearing columbite pseudomorphs and the precipitation of U-rich silicates (up to 34.35 wt.% UO₂), galena, and LREE-rich fluorides within pyrochlore vugs. In contrast to the homogeneous distribution of the primary ore mineralization, the secondary pyrochlore mineralization shows striking zonation, being most intense in the AGB and AGC proximal to a massive cryolite deposit. The U mineralization in the Madeira deposit exhibits grades of 328 ppm UO₂, comparable to the main deposits of this type, with significant reserves of up to 52 kt U. However, it is different from those deposits in four key aspects: homogeneous dispersion of mineralization; pyrochlore as the exclusive primary ore mineral; U and Th mineralizations formed at different stages; and intense hydrothermal alteration. These characteristics are attributed to the special conditions imposed by the fluorine-rich nature of the peralkaline magma. Full article

The Barroso–Alvão region is an excellent setting for studying Li mineralization associated with granitic pegmatites and developing Li exploration techniques. Among the distinguished pegmatite types in this pegmatite field, the spodumene-bearing dyke from Alijó is a representative example of an Iberian Li–Cs–Ta (LCT) pegmatite currently under exploitation. In this work, we examine the internal evolution of the Alijó dyke and its external metasomatic effect on the surrounding metasediments, contributing to lithium exploration techniques. Electron microprobe analyses provided clues about the crystallization conditions and the degree of differentiation of the pegmatitic melt, whereas the external metasomatism induced by the spodumene-bearing pegmatite was studied through whole-rock geochemistry. The obtained results indicate that the primary crystallization of the studied dyke likely occurred at temperatures between 450–500 °C, with emplacement at shallow crustal levels of about 2–3 kbar. The high concentrations of trace elements such as Li, Cs, Rb, Be, Sn, Nb, Ta, Ge, U, and Tl in the pegmatitic melt suggests high availability of these elements, allowing their partitioning into an early exsolved fluid phase. The exsolution of this fluid phase, subtracting components such as F and B, from the pegmatitic melt would cause a significant undercooling of the melt. Moreover, the interaction of this expelled fluid with the country rock generated a metasomatic overprint in the surrounding metasedimentary host rocks. The metasomatic effect in Alijó is strongly influenced by the nature of the host metasediments, with a significantly higher grade of metasomatism observed in pelitic (mica-rich) samples compared to psammitic (mica-poor) samples collected at same distances from the dyke. The greisen developed close to the pegmatite contact reflects this metasomatic signature, characterized by the mobilization of at least B, F, Li, Rb, Cs, Sn, Be, Nb, Ta, and Tl. We cautiously suggest that whole rock Li concentrations greater than 300 ppm, combined with a minimum value of 1000 ppm for the sum of B, F, Li, Rb, Cs, and Sn in pelitic metasediments of Barroso–Alvão, may be indicative of a mineralized pegmatite in this region. Full article

The Weilasituo Li–polymetallic deposit, located on the western slope of the southern Great Xing’an Range in the eastern Central Asian Orogenic Belt, is hosted by quartz porphyry with crypto-explosive breccia-type Li mineralisation atop and vein-type Sn-Mo-W-Zn polymetallic mineralisation throughout the breccia pipe. This study introduces new data on multistage quartz and mica in situ trace elements; the study was conducted using laser ablation inductively coupled plasma mass spectrometry and ⁴⁰Ar/³⁹Ar dating of zinnwaldite to delineate the metallogenic age and genesis of Li mineralisation. Zinnwaldite yields a plateau age of 132.45 ± 1.3 Ma (MSWD = 0.77), representing Early Cretaceous Li mineralisation. Throughout the magmatic–hydrothermal process, quartz trace elements showed Ge enrichment. Li, Al, and Ti contents decreased, with Al/Ti and Ge/Ti ratios increasing, indicating increased magmatic differentiation, slight acidification, and cooling. Mica’s rising Li, Rb, Cs, Mg, and Ti contents and Nb/Ta ratio, alongside its falling K/Rb ratio, indicate the magma’s ongoing crystallisation differentiation. Fractional crystallisation primarily enriched Li, Rb, and Cs in the late melt. Mica’s high Sc, V, and W contents indicate a high f_O2 setting, with a slightly lower f_O2 during zinnwaldite formation. Greisenisation observed Zn, Mg, and Fe influx from the host rock, broadening zinnwaldite distribution and forming minor Zn vein orebodies later. Late-stage fluorite precipitation highlights a rise in F levels, with fluid Sn and W levels tied to magma evolution and F content. In summary, the Weilasituo Li–polymetallic deposit was formed in an Early Cretaceous extensional environment and is closely related to a nearby highly differentiated Li-F granite. During magma differentiation, rare metal elements such as Li and Rb were enriched in residual melts. The decrease in temperature and the acidic environment led to the precipitation of Li-, Rb-, and W-bearing minerals, and the increased F content in the late stage led to Sn enrichment and mineralisation. Fluid metasomatism causes Zn, Mg, and Fe in the surrounding rock to enter the fluid, and Zn is enriched and mineralised in the later period. Full article

Near the Segura pluton, hyper-differentiated magmas enriched in F, P, and Li migrated through shallowly dipping fractures, which were sub-perpendicular to the schistosity of the host Neoproterozoic to Lower Cambrian metasedimentary series, to form two swarms of low-plunging aplite–pegmatite dykes. The high enrichment factors for the fluxing elements (F, P, and Li) compared with peraluminous granites are of the order of 1.5 to 5 and are a consequence of the extraction of low-viscosity magma from the crystallising melt. With magmatic differentiation, increased P and Li activity yielded the crystallisation of the primary amblygonite–montebrasite series and Fe-Mn phosphates. The high activity of sodium during the formation of the albite–topaz assemblage in pegmatites led to the replacement of the primary phosphates by lacroixite. The influx of external, post-magmatic, and Ca-Sr-rich hydrothermal fluids replaced the initial Li-Na phosphates with phosphates of the goyazite–crandallite series and was followed by apatite formation. Dyke emplacement in metasediments took place nearby the main injection site of the muscovite granite, which plausibly occurred during a late major compression event. Full article

Earth observation by remote sensing plays a crucial role in granite extraction, and many current studies use thermal infrared data from sensors such as ASTER. The challenge lies in the low spatial resolution of these satellites, hindering precise rock type identification. A breakthrough emerges with the Thermal Infrared Spectrometer (TIS) on the Sustainable Development Science Satellite 1 (SDGSAT-1) launched by the Chinese Academy of Sciences. With an exceptional 30 m spatial resolution, SDGSAT-1 TIS opens avenues for accurate granite extraction using remote sensing. This study, exemplified in Xinjiang’s Karamay region, introduces the BR-ISauvola method, leveraging SDGSAT-1 TIS data. The approach combines band ratio with adaptive k-value selection using local grayscale statistical features for Sauvola thresholding. Focused on large-scale granite extraction, results show F1 scores above 70% for Otsu, Sauvola, and BR-ISauvola. Notably, BR-ISauvola achieves the highest accuracy at 82.11%, surpassing Otsu and Sauvola by 9.62% and 0.34%, respectively. This underscores the potential of SDGSAT-1 TIS data as a valuable resource for granite extraction. The proposed method efficiently utilizes spectral information, presenting a novel approach for rapid granite extraction using remote sensing TIS imagery, even in scenarios with low spectral resolution and a single data source. Full article

The ability to rapidly and accurately delineate open-pit granite mining areas is pivotal for effective production planning and environmental impact assessment. Over the years, advancements in remote sensing techniques, including the utilization of satellite imagery, LiDAR technology and unmanned aerial vehicles, have revolutionized the way mining areas are monitored and managed. Simultaneously, in the context of the open-pit mining area extraction task, deep learning-based automatic recognition is gradually replacing manual visual interpretation. Leveraging the potential of unmanned aerial vehicles (UAVs) for real-time, low-risk remote sensing, this study employs UAV-derived orthophotos for mining area extraction. Central to the proposed approach is the novel Gather–Injection–Perception (GIP) module, designed to overcome the information loss typically associated with conventional feature pyramid modules during feature fusion. The GIP module effectively enriches semantic features, addressing a crucial information limitation in existing methodologies. Furthermore, the network introduces the Boundary Perception (BP) module, uniquely tailored to tackle the challenges of blurred boundaries and imprecise localization in mining areas. This module capitalizes on attention mechanisms to accentuate critical high-frequency boundary details in the feature map and synergistically utilizes both high- and low-dimensional feature map data for deep supervised learning. The suggested method demonstrates its superiority in a series of comparative experiments on a specially assembled dataset of research area images. The results are compelling, with the proposed approach achieving 90.67% precision, 92.00% recall, 91.33% F1-score, and 84.04% IoU. These figures not only underscore the effectiveness of suggested model in enhancing the extraction of open-pit granite mining areas but also provides a new idea for the subsequent application of UAV data in the mining scene. Full article

This paper reports the results from an investigation on the geochemistry and petrogenesis of the Aptian Li-F granites from the Omchikandya, Burgali, and Arga Ynnakh Khaya ore fields in the northern Verkhoyansk–Kolyma orogenic belt in eastern Russia. Li-F microcline–albite granites intrude the Late Jurassic to Early Cretaceous syn-collisional granitoids. According to their geochemical composition, they are close to A-type granites and can be subdivided into low-P and high-P varieties, differing in their geochemistry and genesis. The low-P microcline–albite granites (Omchikandya massif) intrude syn-collisional biotite granites. It is assumed that the formation of their parent melt occurred at deep levels in the same magma chamber that produced biotite granites. The high-P granites (Verkhne–Burgali ethmolith and Kester harpolith) are supposed to have been derived from melts originated from a high-grade metamorphosed lower crustal protolith under the influence of deep-seated fluid flows related to diapirs of alkaline-ultrabasic or alkaline-basic composition. It is supposed that their formation was related to post-collisional extension during the early stages of the evolution of the Aptian–Late Cretaceous Indigirka belt of crust extension. All studied Li-F granites are enriched with rare metals and have associated Li deposits with accompanying Sn, W, Ta, and Nb mineralization. In the low-P Li-F Omchikandya massif, mineralization tends to occur within greisenized granites and greisens in their apical parts. In the high-P granite massifs, mineralization is found throughout their volume, and, therefore, the Verkhne–Burgali ethmolith and Kester harpolith can be considered as large ore bodies. There is a direct dependence of the content and reserves of Li₂O on the content of P₂O₅. Minimum Li₂O reserves are established in low-P Li-F microcline–albite granites of the Polyarnoe deposit of the Omchikandya ore field, whereas in the high-P granites of the Verkhne–Burgali and Kester deposits, the Li₂O reserves are significantly higher. Full article

A dataset of >1190 published compositional analyses of muscovite from granitic pegmatites of varying mineralogical types was compiled to reevaluate the usefulness of K-Rb-Li systematics of muscovite as a tool for distinguishing mineralogically simple pegmatites from pegmatites with potential Li mineralization. Muscovite from (i) common, (ii) (Be-Nb-Ta-P)-enriched, (iii) Li-enriched, and (iv) REE- to F-enriched pegmatites contain Li contents that vary between 10 and 20,000 ppm depending on the degree of pegmatite fractionation. Common pegmatites are characterized by low degrees of fractionation as exhibited by K/Rb ratios ranging from 618 and 25 and Li contents generally being <200 ppm but infrequently as high as 743 ppm in muscovite. Moderately fractionated pegmatites with Be, Nb, Ta, and P enrichment contain muscovite having K/Rb ratios mostly between 45 and 7 plus Li contents between 5 to >1700 ppm. Muscovite from moderately to highly fractionated Li-rich pegmatites exhibit a wide range of K/Rb ratios and Li values: (i) K/Rb = 84 to 1.4 and Li = 35 to >18,100 ppm for spodumene pegmatites, (ii) K/Rb = 139 to 2 and Li = 139 to >18,500 ppm for petalite pegmatites, and (iii) K/Rb = 55 to 1.5 and Li = 743 to >17,800 ppm for lepidolite pegmatites. Pegmatites that host substantial REE- and F-rich minerals may carry muscovite with K/Rb ratios between 691 to 4 that has Li contents between 19 to 15,690 ppm. The K/Rb-Li behavior of muscovite can be useful in assessing the potential for Li mineralization in certain granitic pegmatite types. The proposed limits of K/Rb values and Li concentrations for identifying spodumene- or petalite-bearing pegmatites as part of an exploration program is reliable for Group 1 (LCT) pegmatite populations derived from S-type parental granites or anatectic melting of peraluminous metasedimentary rocks. However, it is not recommended for application to Group 2 (NYF) pegmatites affiliated with anorogenic to post-orogenic granitoids with A-type geochemical signatures or that derived by the anatexis of mafic rocks that generated REE- and F-rich melts. Full article

The Lijiagou pegmatite spodumene deposit, located in the middle of the Songpan–Garze Fold Belt and southeast of the Ke’eryin ore field, is a newly discovered super-large deposit. In order to reveal the metallogenic tectonic environment and evolution process of pegmatite, based on the study of the geological characteristics of pegmatite, we carried out a whole-rock geochemical analysis of Ke’eryin two-mica granite and Lijiagou pegmatite and carried out a detailed electron probe microanalysis (EPMA) and laser ablation inductively coupled plasma mass spectrometry (LA-ICPMS) analysis of mica minerals in each zonal pegmatite. The results show that the Ke’eryin two-mica granite is mainly formed in the transition period from syn-collision to post-collision. After the end of the continental collision, the crust is squeezed and thickened in the post-collision extensional transition tectonic environment. Mica from the microcline pegmatite zone (MP) to the albite spodumene pegmatite zone (ASP) in pegmatite show different compositions and structural characteristics, with the evolution trend in the direction from muscovite to Li-bearing mica. The type of mica from MP to AP is mainly muscovite, and Li-bearing mica appears in ASP, which is secondary and metasomatic at the edge of primary muscovite. From MP to ASP, there was a negative correlation between Nb/Ta, K/Rb and the Li, Rb, and Cs contents of mica, while the contents of Li, Rb, Cs, and F in the Li-bearing mica of ASP increased sharply. This evidence illustrates that the favorable tectonic environment contributed to the formation of the Lijiagou pegmatitic spodumene deposit. Lijiagou pegmatite experienced the magmatic–hydrothermal evolution process and has a high degree of differentiation and evolution from MP to ASP, which gradually increased. Combined with the change in mica type, it is considered that ASP formed from the stage of magmatic transition to hydrothermal and was a hydrothermal environment, and Li, Rb, and Cs mainly began to enrich at the stage of magmatic–hydrothermal transition. Full article

In the present study, we extensively explored the high-pressure behaviors and vibrational properties of amblygonite LiAlPO₄F with elevated pressures up to 34.3 GPa based on single-crystal X-ray diffraction measurements, Raman spectroscopy, and DFT calculations. The compressibility and elastic properties of amblygonite were determined first. Specifically, the obtained isothermal bulk modulus of LiAlPO₄F is 128(4) GPa and the triclinic phase exhibited anisotropic compression with axial compressibility β_c > β_a > β_b with a ratio of 1.11:1.00:1.20. The Raman spectra showed no indication of phase transformation and were used to obtained mode Grüneisen parameters. The average Grüneisen parameter for PO₄ tetrahedral sites was smaller than for the LiO₄F sites. Our results provide new insights into the phase stability and elastic properties of lithium-fluorite granites at extreme conditions. Full article

Gabal El-Ineigi fluorite-bearing rare-metal granite with A-type affinity, located in the Central Eastern Desert of Egypt, is distinguished by its abundance of large fluorite-quartz veins and mafic enclaves. Plagioclase (labradorite to oligoclase), Mg-rich biotite, and Mg-rich hornblende are the main components of mafic enclaves, with significant amounts of fluorite as essential phases, and titanite and Fe-Ti oxides (Nb-free rutile and ilmenite-rutile solid solution) as the main accessories. These enclaves are monzodioritic in composition, Si-poor, and highly enriched in Ca, Fe, Mg, and F compared to the host alkali feldspar F-poor Si-rich granites. Given the conflicting evidence for a restitic, xenolithic, magma mixing/mingling, cumulate, or bimodal origin for these enclaves, we propose that the mafic enclaves and felsic host granites are two conjugate liquids, with contrasting compositions, of a single parental melt. This is inferred by the normalized REE patterns that are similar. As a result, liquid immiscibility is proposed as a probable explanation for this mafic–felsic rock association. These enclaves can be interpreted as transient melt phases between pure silicate and calcium-fluoride melts that are preserved from the early stages of separation before evolving into a pure fluoride (Ca-F) melt during magma evolution. Due to element partitioning related to melt unmixing, the enclaves are preferentially enriched in Ca, F, Li, Y, and REE and depleted in HFSE (such as Zr, U, Th, Ta, Nb, Hf, and Ga) in comparison to the host granites. Furthermore, mafic enclaves exhibit W-type tetrad effects, while host granites exhibit M-type tetrad effects, implying that the REE partitioning, caused by liquid immiscibility, is complementary. Full article