Search Results (192)

The Songpan–Ganzi Orogenic Belt (SGOB) is bounded by the South China, North China, and Qiangtang blocks and forms the eastern margin of the Tibetan Plateau. The Tiechanghe Granite is located at the junction of the southeast margin of the SGOB and the western margin of the Yangtze Block. To elucidate the genetic relationship between the Tiechanghe Granite and the surrounding molybdenum deposits in Western Sichuan, in this study, we conducted zircon U-Pb and molybdenite Re-Os isotopic dating. The results indicate that the Tiechanghe Granite predominantly consists of monzogranite, with minor occurrences of syenogranite, while the molybdenum deposits are mainly found in skarn and quartz veins. The laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS) zircon U-Pb ages of the Tiechanghe Granite range from 162.9 ± 0.7 Ma (MSWD = 0.31, n = 25) to 163.4 ± 0.6 Ma (MSWD = 0.85, n = 26), and the LA-ICP-MS zircon U-Pb age of the pegmatite veins is 164.1 ± 0.9 Ma (MSWD = 1.3, n = 19). These ages are consistent with the weighted average Re-Os age of the Ziershi molybdenite (160.3 ± 1.6 Ma, n = 2) within the error margins. These findings and previously obtained magmatic and metallogenic ages for the region suggest that a magmatic and mineralization event involving granite, molybdenum, tungsten, and copper occurred at around 162–164 Ma in the study area. This discovery broadens the exploration perspective for mineral resources in the Jiulong area of Western Sichuan and the entirety of Western Sichuan. Full article

Quickly determining the metal content in plants and subsequently identifying geochemical anomalies can provide clues and guidance for predicting the location and scale of concealed ore bodies in vegetation-covered areas. Although visible, near-infrared and shortwave infrared (VNIR–SWIR) reflectance spectroscopy at wavelengths ranging from 400 to 2500 nm has been proven by many researchers to be a fast, accurate and nondestructive approach for estimating the contents of copper (Cu), lead (Pb), zinc (Zn) and other metal elements in plants, relatively few studies have been conducted on the estimation of lithium (Li) in plants. Therefore, the potential of applying VNIR–SWIR spectroscopy techniques for estimating the Li content in plants was explored in this study. The Jingerquan Li mining area in Hami, Xinjiang, China, was chosen. Three sampling lines were established near a pegmatite deposit and in a background region, canopy reflectance spectra were obtained for desert plants and Li contents were determined in the laboratory; then, quantitative relationships were established between nine different transformed spectra (including both integer and fractional orders) and the Li content was estimated using partial least squares regression (PLSR). The results showed that models constructed using high-order derivative spectra (with an order greater than or equal to 1) significantly outperformed those based on original and low-order derivative spectra (with an order less than 1). Notably, the model based on a 1.1-order derivative spectrum displayed the best performance. Furthermore, the performance of the model based on the two-layer wavelet coefficients of the 1.1-order derivative spectrum was further improved compared with that of the model based on only the 1.1-order derivative spectrum. The coefficient of determination ($R_{pre}^2$) and the ratio of performance to deviation (RPD) for the validation set increased from 0.6977 and 1.7656 to 0.7044 and 1.8446, respectively, and the root mean square error (RMSEpre) decreased from 2.5735 to 2.4633 mg/kg. These results indicate that quickly and accurately estimating the Li content in plants via the proposed spectroscopic analysis technique is feasible and effective; however, appropriate spectral preprocessing methods should be selected before hyperspectral estimation models are constructed. Overall, the developed hybrid spectral transformation approach, which combines wavelet coefficients and derivative spectra, displayed excellent application potential for estimating the Li content in plants. Full article

A significant amount of pegmatite has been discovered on the northwest margin of the Qaidam basin. Among this, the Jiaolesayi pegmatite, located in the northwestern margin of the Quanji Massif (Oulongbuluke micro-continent), shows rare element mineralization potential. Detailed field investigations, along with mineralogical, geochemical, and zircon U-Pb geochronological studies, were carried out on the pegmatite. The results show that the Jiaolesayi pegmatite is syenite, without obvious compositional zoning in the outcrop. It exhibits a peraluminous, high-K calc-alkaline nature with strong depletions in Eu, Sr, Ba, Ti, and P, and high contents of Nb, Ta, Y, Ti, U, Th, and heavy rare earth elements (HREEs), which are primarily concentrated in allanite-(Ce), euxenite-(Y), limonite, thorite, and zircon. The geochemical and mineralogical features of the syenite pegmatite indicate it belongs to the euxenite-type in the rare element class (REE) of the NYF family, with the characteristic accessory mineral being euxenite-(Y). Its 10,000 Ga/Al ratios (2.46 to 2.96), Zr + Nb + Ce + Y contents (998 to 6202 ppm), Y/Nb ratios (0.62 to 0.75), and Yb/Ta ratios (0.80 to 1.49) show an affinity with A₁-type granite. Zircons from the syenite sample yielded a weighted mean ²⁰⁶Pb/²³⁸U age of 413.6 ± 1.4 Ma, while the elevated U and Th concentrations in the zircons and Th/U ratios (0.04 to 0.16) suggest the possible influence of hydrothermal processes in the late-stage fractional crystallization. In the context of the regional tectonic evolution, the syenite pegmatite may have formed from a basic alkaline magma derived from an OIB-like melt with minor crustal contamination, under the post-collisional extension setting. Full article

The Marun–Keu complex plays a significant role in our understanding of the geological evolution of the Ural orogen; however, it remains poorly understood. This study aims to provide insights into the complex’s age, protolith composition, rock formation conditions, and its position in the geological history. The zircons from the host granitic gneiss are characterized by magmatic cores with an age of 473 Ma and metamorphic rims with an age of approximately 370 Ma. We suggest that the metamorphic rims were formed during eclogite metamorphism and that the metagranitoids hosting the eclogites experienced eclogite metamorphism simultaneously with the basic and ultrabasic rocks that are common in this area. Heterogeneous zircons were also isolated from the selvage of a pegmatite vein, in which four domains are distinguished, two to three of which can be identified within single grains, as follows: (1) igneous cores with an age of approximately 470 Ma and the geochemical characteristics of zircon crystallized in basic rocks; (2) zircons recrystallized during eclogite metamorphism with geochemical characteristics intermediate between those of the magmatic cores and true eclogitic zircon; (3) pegmatitic zircon, exhibiting the most sharply differentiated REE spectra of all four domains, characterized by a prominent positive Ce anomaly and a weakly expressed negative Eu anomaly; and (4) eclogitic zircon, observed in the form of veins and rims, superimposed in relation to the other three domains. The age of the latter three domains is within the error range and is estimated to be approximately 370 Ma. This indicates that the processes of eclogite metamorphism and the formation of pegmatites occurred at approximately the same time in the studied area. Full article

Himalayan leucogranite is an excellent target for understanding the orogenic process of the India–Asia collision, but its origin and tectonic significance are still under debate. An integrated study of geochronology, geochemistry, and in situ Sr-Nd-Hf isotopes was conducted for a tourmaline-bearing leucogranite in the eastern Tethyan Himalaya using LA-ICP-MS, X-ray fluorescence spectroscopy, and ICP-MS and LA-MC-ICP-MS, respectively. LA-ICP-MS U-Pb dating of zircon and monazite showed that it was emplaced at ~19 Ma. The leucogranite had high SiO₂ and Al₂O₃ contents ranging from 73.16 to 73.99 wt.% and 15.05 to 15.24 wt.%, respectively. It was characterized by a high aluminum saturation index (1.14–1.19) and Rb/Sr ratio (3.58–6.35), which is characteristic of S-type granite. The leucogranite was enriched in light rare-earth elements (LREEs; e.g., La and Ce) and large ion lithophile elements (LILEs; e.g., Rb, K, and Pb) and depleted in heavy rare-earth elements (e.g., Tm, Yb, and Lu) and high field strength elements (HFSEs; e.g., Nb, Zr, and Ti). It was characterized by high I Sr (t) (0.7268–0.7281) and low ε Nd (t) (−14.6 to −13.2) and ε Hf (t) (−12.6 to −9.47), which was consistent with the isotopic characteristics of the Higher Himalayan Sequence. Petrogenetically, the origin of the leucogranite is best explained by the decompression-induced muscovite dehydration melting of an ancient metapelitic source within the Higher Himalayan Sequence during regional extension due to the movement of the South Tibetan Detachment System (STDS). The significantly high lithium and beryllium contents of the leucogranite and associated pegmatite suggest that Himalayan leucogranites possess huge potential for lithium and beryllium exploration. 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

Previous studies on the Ke’eryin pegmatite-type lithium ore field in the Songpan–Ganzi Orogenic Belt have explored the characteristics of the parent rock but have not precisely determined its magma source area. This uncertainty limits our understanding of the regularity of lithium ore formation in this region. In this study, to address the issue of the precise source area of the parent rock of lithium mineralization, a detailed analysis of the Li isotope composition of the ore-forming parent rock (Ke’eryin two-mica monzogranite) and its potential source rocks (Triassic Xikang Group metamorphic rocks) was conducted. The δ⁷Li values of the Ke’eryin two-mica monzogranite, Xikang Group metasandstone, and Xikang Group mica schist are −3.3–−0.7‰ (average: −1.43‰), +0.1–+6.9‰ (average: +3.83‰), and −9.1–0‰ (average: −5.00‰), respectively. The Li isotopic composition of the Ke’eryin two-mica monzogranite is notably different from the metasandstone and aligns more closely with the mica schist, suggesting that the mica schist is its primary source rock. The heavy Li isotopic composition of the two-mica monzogranite compared to the mica schist may have resulted from the separation of the peritectic garnet into the residual phase during the biotite dehydration melting process. Moreover, the low-temperature weathering of the source rocks may have been the main factor leading to the lighter lithium isotope composition of the Xikang Group mica schist compared to the metasandstone. Further analysis suggests that continental crust weathering and crustal folding and thickening play crucial roles in the enrichment of lithium during multi-cycle orogenies. Full article

A modified model based on classical nucleation theory was applied to a natural hydrous peraluminous pegmatite composition and tested against crystallization experiments in order to further investigate the quantification of nucleation delay in felsic melts. Crystallization experiments were performed in a piston-cylinder apparatus at 630 MPa and temperatures between 650 and 1000 °C for durations ranging from 0.3 to 211 h. Experimental run products were investigated by scanning electron microscopy paired with energy dispersive spectroscopy analyses of both crystalline and quenched liquid phases, the results of which were compared to an established theoretical nucleation delay model from the literature. The experiments showed good agreement (within a factor of 5) with the model for quartz, while it showed moderate agreement (within a factor of 10) with the model for sodic feldspar. Other crystals also nucleated, demonstrating abundant features of disequilibrium. Our research further demonstrates the potential of the model to predict nucleation delay, showing promising results for the quantification of the nucleation delay of quartz and feldspar in natural felsic melts, thus adding to previously published studies on hydrous, metaluminous, felsic melts and dry basaltic melts. Full article

Tourmaline, a boron-bearing mineral, has been extensively applied as a geothermometer, provenance indicator, and fluid-composition recorder in geological studies. In this paper, the decomposition capability of an HF-HNO₃–mannitol mixture for a tourmaline sample was investigated in detail for the first time, and a wet acid digestion method based on the boron–mannitol complex for accurate boron determination in tourmaline by inductively coupled plasma mass spectrometry (ICP-MS) was proposed. With a digestion temperature of 140 °C, tourmaline samples of 25 mg (±0.5 mg) can be completely decomposed by a ternary mixture, which consisted of 0.6 mL of HF, 0.6 mL of HNO₃, and 0.7 mL of 2% mannitol (wt.), via a continuous heating treatment of 36 h. Following gentle evaporation at 100 °C, the sample residues were re-dissolved using 2 mL of 40% HNO₃ solution (wt.) and diluted to about 2.0 × 10⁵-fold by a two-step method using 2% HNO₃ solution (wt.). The boron contents in a batch of parallel tourmaline samples were then determined by ICP-MS, and results showed that the boron concentration levels were in a range of 3.20–3.44% with determination RSDs less than 4.0% (n = 5). It was found that the boron concentrations obtained at the mass of ¹⁰B were comparable with results from the measurements at the mass of ¹¹B. This revealed that the usage of 2% mannitol with a quantity as high as 0.7 mL in this developed approach did not exhibit significant effect on the quantification accuracy of boron at the mass of ¹¹B. It was also found that the processes including fluoride-forming prevention and fluoride decomposition deteriorated the boron-reserving efficiency of mannitol for tourmaline, causing the averaged boron contents to vary from 2.25% to 3.57% (n = 5). Furthermore, the stability of the boron–mannitol complex under 185 °C by applying the laboratory high pressure-closed digestion method was evaluated, which showed that there existed a 60.36% loss of boron compared to that under 140 °C by using this proposed approach. For this ternary mixture, the tourmaline decomposing efficiency was found to be weakened prominently using 100 °C as the digestion temperature, and tourmaline powders can be observed even after 72 h of continuous heating with B contents within 1.09–1.23% (n = 5). To assess the accuracy of this developed method, the boron recovery of anhydrous lithium tetraborate was studied. It was found that the boron recoveries were within 96.59–102.12% (RSD < 1%, n = 5), demonstrating the accuracy and reliability of this proposed method, which exhibits advantages of high B preserving efficiency, and giving concentration information of both B and trace elements simultaneously. By applying such a boron–mannitol complex-based wet acid digestion method, the chemical composition of boron and trace elements in three tourmaline samples from different pegmatites were quantified, which provided valuable information to distinguish regional deposits and the associated evolution stages. Full article

The Central Altun orogenic system is a result of the amalgamation of multiple micro-continental blocks and island arcs. This complex system originated from subduction–accretion–collision processes in the Proto-Tethys Ocean during the Early Paleozoic. Research has reported the discovery of several Li-Be granitic pegmatite deposits in the Central Altun Block, including the North Tugeman granitic pegmatite Li-Be deposit, Tugeman granitic pegmatite Be deposit, Tashisayi granitic pegmatite Li deposit, South Washixia granitic pegmatite Li deposit, and Tamuqie granitic pegmatite Li deposit. The Tashidaban granitic pegmatite Li deposit has been newly discovered along the northern margin of the Central Altun Block. Field and geochemical studies of the Tashidaban granitic pegmatite Li deposit indicate: (1) Spodumene pegmatites and elbaite pegmatites, as Li-bearing granitic pegmatites that form the Tashidaban granitic pegmatite Li deposit, intrude into the two-mica schist, and marble of the Muzisayi Formation of the Tashidaban Group. (2) Columbite–tantalite group minerals and zircon U-Pb dating results indicate that the mineralization age of Tashidaban Li granitic pegmatites is 450.2 ± 2.4 Ma with a superimposed magmatic event at around 418–422 Ma later. (3) Whole-rock geochemical results indicate that the Kumudaban rock sequence belongs to the S-type high-K to calc-alkaline granites and the Tashidaban Li granitic pegmatites originated from the extreme differentiation by fractional crystallization of the Kumdaban granite pluton. Full article

The Sidi Bou Othmane (SBO) pegmatite district is situated in the Central Jebilet massif, Western Meseta domain, Morocco. The SBO district is hosted essentially in a volcano-sedimentary series composed of Late-Devonian Sarhlef shales. Pegmatite bodies crop out as dykes, which are oriented from N-S to E-W and are generally variably deformed with ductile and/or brittle structures with ante, syn- or post-kinematic criteria. Petrographic observations of pegmatite dykes show that feldspars (i.e., albite, microcline) are the most abundant mineral phases, followed by quartz and micas, with tourmaline and accessory minerals such as garnet, and zircon also featuring heavily, as well as secondary minerals such as clinochlore, sericite, and illite. The geochemical study of the SBO pegmatites indicates that they have mainly S-type granitic compositions, which are peraluminous granites with calc-alkalic affinities. The study of trace elements indicates that SBO pegmatites were formed in post-orogenic syn-collision context during the Variscan orogeny by the partial melting of argilliferous sediment. They can be ascribed to the muscovite-bearing pegmatite; moreover, they have good potential regarding ceramics. They also contain minerals, such as feldspar, which have been recently assessed as critical raw materials by the European Union. Full article

Gold occurrence Maljavr is the first Archean conglomerate-hosted gold mineralization found in the Fennoscandian Shield. Gold-mineralized metasomatic rocks form a set of lenses within a 10 m thick linear zone, conformable to the bedding of host conglomerates. The lenses are up to 10 m long and up to 1 m thick and they clearly exhibit three alteration envelopes: the rock in the central part consists of garnet and quartz or garnet-only; biotite, garnet, and quartz make the intermediate biotite–garnet envelope; hornblende, hedenbergite, and quartz are the principal rock-forming minerals in the outer zone of the lenses. All metasomatic rocks contain sulfide mineralization up to 15–20 vol.% and up to 0.6 g/t Au. The main ore mineral is pyrrhotite, and the minor minerals are arsenopyrite, chalcopyrite, pentlandite, löllingite, and troilite. The age of zircon from biotite gneiss in the zone of alteration is 2664 ± 18 Ma, this is considered as the time of formation of lenses of metasomatic rocks. Biotite gneiss-conglomerate and metasomatic rocks were later intruded by tourmaline granite pegmatite 2508 ± 7 Ma. The injection of pegmatite caused re-crystallization of sulfides (mainly arsenopyrite and löllingite) and redistribution of gold. Visible gold in association with Bi minerals native bismuth, ehrigite, maldonite, bismuthinite, joseite-B, and hedleyite was found in inclusions in recrystallized arsenopyrite and löllingite. Au content in the rocks with recrystallized arsenopyrite and löllingite is >1 g/t, up to 30 g/t in hand samples. The 2508 Ma pegmatite is interpreted as synchronous with formation of gold mineralization in its present form. The linkage of gold mineralization with pegmatite and geochemical association Au-As-Se-Te-Bi in the mineralized rocks agree with characteristics of intrusion-related gold deposits worldwide. Biotite gneiss–metaconglomerate, hosting the mineralized altered rocks, was the probable primary source of arsenic and gold for mineralization. Full article

Madagascar is globally recognized as an important producer of high-quality flaky graphite. However, current research on graphite deposits in Madagascar remains insufficient. Previous studies have linked the genesis of Madagascan graphite deposits to the metamorphism of sedimentary organic matter. Here, we provide a case study of graphite deposits in Madagascar, combining new data from the Ambahita graphite deposit (AMG) in southern Madagascar with data from the Antanisoa graphite deposit (ANG) in central Madagascar and the Vohitasara graphite deposit (VOG) on the east coast of Madagascar. We note that the mineral assemblages of graphite-bearing rocks in the AMG, ANG, and VOG are not typical of metamorphic mineral assemblages but rather the results of filling and metasomatism by mantle-derived fluids that occurred after peak metamorphism. Electron microprobe analysis indicates that the graphite of the AMG, VOG, and ANG is usually associated with phlogopite or Mg-biotite; the phlogopite shares a common genesis with other widespread phlogopite deposits across Madagascar. We reveal that the distribution of graphite deposits in Madagascar is primarily controlled by ductile shear zones between blocks. Ductile shear zones that extend deep into the mantle can provide an ideal migration channel and architecture for the emplacement of mantle-derived fluids. The graphite mineralization formed no earlier than the peak metamorphism (490 Ma) and no later than the intrusion of pegmatite veins (389 ± 5 Ma). The distribution of graphite deposits, graphite orebody morphologies, mineral associations, and geochemical data suggest that the genesis of graphite deposits in Madagascar is linked to mantle-derived fluid filling rather than the metamorphism of sediments, as previously suggested. These findings have important implications for similar deposits in Madagascar and potentially globally. Full article

Beryl mineralization in the Nugrus-Sikait domain in the South Eastern Desert (SED) of Egypt occurs as disseminated crystals in granitic pegmatite and quartz, as well as pegmatite veins crosscutting mélange schist and ophiolitic rocks. When granitic pegmatite comes into contact with the ophiolitic rocks, phlogopite and amphibole schists are formed due to K metasomatism. The ophiolitic mélange is intruded by leucogranite and related pegmatite along the NNW to NW Nugrus shear zone. Beryl samples have been collected from Um Sleimat, Madinat Nugrus, Wadi Abu Rusheid, and Wadi Sikait. Major oxides and in situ trace and rare earth elements (REEs) of beryl and associated minerals were analyzed through EPMA and LA-ICP-MS, respectively. The investigated beryl, based on its color and chemical compositions, can be classified into the two following types: pegmatitic beryl (type I) and schist-related beryl (type II). The former is colorless to pale green, and is mainly restricted in pegmatite veins; it is poor in Cr₂O₃ (up to 0.03 wt%) and MgO (Nil). The latter, deep green in color, is rich in Cr₂O₃ (up to 0.27 wt%) and MgO (up to 2.71 wt%), and occurs within quartz veins, phlogopite schists, and tremolite schists. The abundant beryl mineralization in phlogopite schists and their related quartz veins suggests that granite and associated pegmatite are the source rocks for the Be-bearing fluids that migrate along the NW-SE trending deep-seated tectonic zone, such as the Nugrus shear zone. Therefore, the formation of beryl in schists is attributed to the interaction of granitic/pegmatitic-derived Be-bearing fluids with serpentinite and gabbro interlayered with mélange schists. Variations in the trace and REE contents of both beryl types (I and II) indicate their two-stage formation from different compositions of Be-rich fluids, where light REEs, Zr, Nb, Ba, and Th decrease from type I beryl to type II. These two phases of beryl could be attributed to the magmatic/hydrothermal fluids associated with the pegmatite emplacement. The early phase of the late-stage magmatic-derived fluids was closely related to magma evolution and pegmatite formation, forming euhedral type I beryl. The late phase of pegmatite-derived fluids was mixed with serpentinite/schist-derived fluids that cause high V and Cr content in type II beryl. The composition of parent magmas of felsic rocks, the high degree of magma fractionation or the late stage melts, fluid compositions (rich in Be, Li, Cs, Rb, K), and alkali metasomatism, as well as the linear NW-SE trending deep-seated shear zone, are all factors possibly influencing beryl mineralization in the SED of Egypt. Full article

The Neoproterozoic period in the Jabal Sayid and Dayheen areas is characterized by three distinct magmatic phases: an early magmatic phase of granodiorite–diorite association, a transitional magmatic phase of monzogranites, and a highly evolved magmatic phase of peralkaline granites and associated pegmatites. The presence of various accessory minerals in the peralkaline granites and pegmatites, such as synchysite, bastnaesite, xenotime, monazite, allanite, pyrochlore, samarskite, and zircon, plays an important role as contributors of REEs, Zr, Y, Nb, Th, and U. The geochemical characteristics indicate that the concentration of these elements occurred primarily during the crystallization and differentiation of the parent magma, with no significant contributions from post-magmatic hydrothermal processes. The obtained geochemical data shed light on the changing nature of magmas during the orogenic cycle, transitioning from subduction-related granodiorite–diorite compositions to collision-related monzogranites and post-collisional peralkaline suites. The granodiorite–diorite association is thought to be derived from the partial melting of predominantly metabasaltic sources, whereas the monzogranites are derived from metatonalite and metagraywacke sources. The peralkaline granites and associated pegmatites are thought to originate from the continental crust. It is assumed that these rocks are formed by the partial melting of metapelitic rocks that are enriched with rare metals. The final peralkaline phase of magmatic evolution is characterized by the enrichment of the residual melt with alkalis (such as sodium and potassium), silica, water, and fluorine. The presence of liquid-saturated melt plays a decisive role in the formation of pegmatites. Full article