Search Results (213)

The Chating Cu-Au and Magushan Cu-Mo deposits in Anhui province are two representative deposits within the recently defined Nanling-Xuancheng ore concentration area in the Middle and Lower Yangtze River Metallogenic Belt (MLYB). Magmatism and mineralization for the area are not well known at present due to a lack of in-depth studies on the petrogenesis of ore-bearing intrusive rocks and their relationship with deposits. Here, the ore-bearing intrusive rocks of the two deposits are investigated through analyses of whole-rock geochemistry and Sr-Nd isotopes, zircon U-Pb ages, and zircon Hf isotopes. The results reflect the two intrusions, both formed in the Early Cretaceous (138.9 ± 0.8 Ma and 132.2 ± 1.3 Ma). They belong to the sub-alkaline high-K calc-alkaline series, while trace elements are enriched in LILEs and LREE and depleted in HFSEs. However, the intrusions of the Chating deposit (I_sr = 0.7064–0.7068; ε_Nd(t) = −8.5–−7.3; ε_Hf(t) = −11.9–−7.0) have obviously different Sr-Nd-Hf isotopic compositions from the intrusions of the Magushan deposit (I_sr = 0.7079–0.7081; ε_Nd(t) = −5.7–−5.4; ε_Hf(t) = −5.4–−3.6). The characteristics indicate that the two intrusions were formed in the same diagenetic ages and tectonic settings and derived from a crust–mantle mixture with predominant mantle-derived materials. But the crust materials of sources are different, which further leads to different metallogenic elements, showing that the Chating deposit is enriched in Cu and Au, while the Magushan deposit is enriched in Mo. Moreover, the characteristics and magma sources of two intrusions and metallogenic elements correspond respectively to the Tongling Cu-Au polymetallic ore concentration area in the MLYB and the southern Anhui Mo polymetallic ore concentration area in the Jiangnan orogen. The correlation implies differences in magmatism and mineralization between the northwestern and southeastern parts of the Nanling-Xuancheng ore concentration area, demarcated by the Jiangnan Deep Fault. These variations were mainly controlled by the Pre-Sinian crustal basement. Full article

Mineral characterization of gold-bearing metasomatites in the Khaptasynnakh ore zone of the Anabar Shield is provided in detail. The following ore formation sequence of mineral associations in the Khaptasynnakh zone was found: pyrite and pyrrhotite → gersdorffite and molybdenite → chalcopyrite, sphalerite, and galena → bornite and chalcocite → tellurides, native gold, stibnite, cinnabar, and native bismuth. Native gold is characterized by varying fineness (550 to 926‰) and Cu impurity (up to 7.87%) values. Most often, it forms symplectite intergrowths with Au telluride–calaverite. Native gold and Au tellurides showed inclusions of chalcocite, bornite, altaite, tellurobismuthite, rickardite, petzite, and clausthalite. A two-stage formation process of the examined gold is suggested: Low-fineness gold was introduced into the system during early potassium metasomatism, while higher-fineness gold related to silica metasomatism resulted from its additional mobilization by fluid during late-stage formation. The low-temperature gold–telluride association observed in the mineral paragenesis of ore-bearing rocks, as well as its inclusions in native gold, suggests epithermal gold–telluride mineralization. Mineral inclusions examined in placer gold validate a genetic relation between the examined ores and gold placers in the Khaptasynnakh ore zone. Full article

The Mazenod Lake region of the southern Great Bear Magmatic Zone (GBMZ) of the Northwest Territories, Canada, comprises the north-central portion of the Faber volcano-plutonic belt. Widespread and abundant surface exposure of several coalescing hydrothermal systems enables this paper to document, without ambiguity, the relationships between geology, structure, alteration, and mineralization in this well exposed iron-oxide–copper–gold (IOCG) mineral system. Mazenod geology comprises rhyodacite to basaltic-andesite ignimbrite sheets with interlayered volcaniclastic sedimentary rocks dominated by fine-grained laminated tuff sequences. Much of the intermediate to mafic nature of volcanic rocks is masked by low-intensity but pervasive metasomatism. The region is affected by a series of coalescing magmatic–hydrothermal systems that host the Sue–Dianne magnetite–hematite IOCG deposit and several related showings including magnetite, skarn, and iron oxide apatite (IOA) styles of alteration ± mineralization. The mid to upper levels of these systems are exposed at surface, with underlying batholith, pluton and stocks exposed along the periphery, as well as locally within volcanic rocks associated with more intense alteration and mineralization. Widespread alteration includes potassic and sodic metasomatism, and silicification with structurally controlled giant quartz complexes. Localized tourmaline, skarn, magnetite–actinolite, and iron-oxide alteration occur within structural breccias, and where most intense formed the Sue–Dianne Cu-Ag-Au diatreme-like breccia deposit. Magmatism, volcanism, hydrothermal alteration, and mineralization formed during a negative tectonic inversion within the Wopmay Orogen. This generated a series of oblique offset rifted basins with continental style arc magmatism and extensional structures unique to GBMZ rifting. All significant hydrothermal centers in the Mazenod region occur along and at the intersections of crustal faults either unique to or put under tension during the GBMZ inversion. Full article

Artisanal and small-scale gold mining (ASGM) poses significant environmental challenges globally, particularly due to mercury (Hg) use. As an example, in Ecuador, Hg use still persists, despite its official ban in 2015. This study investigated the geogenic and anthropogenic contributions of potentially toxic elements (PTEs) in the Ponce Enriquez Mining District (PEMD), a region characterized by hydrothermally altered basaltic bedrock and Au-mineralized quartz veins. To assess local baseline values and identify PTE-bearing minerals, a comprehensive geochemical, mineralogical, and petrographic analysis was conducted on bedrock and mineralized veins. These findings reveal distinct origins for the studied PTEs, which include Hg, As, Cu, Ni, Cr, Co, Sb, Zn, and V. Specifically, Hg concentrations in stream sediments downstream (up to 50 ppm) far exceed natural bedrock levels (0.03–0.707 ppm), unequivocally indicating significant anthropogenic input from gold amalgamation. Furthermore, copper shows elevated concentration primarily linked to gold extraction. Conversely, other elements like As, Ni, Cr, Co, Sb, Zn, and V are primarily exhibited to be naturally abundant in basalts due to the presence of primary mafic minerals and to hydrothermal alterations, with elevated concentrations particularly seen in sulfides like pyrite and arsenopyrite. To distinguish natural geochemical anomalies from mining-related contamination, especially in volcanic terrains, this study utilizes Upper Continental Crust (UCC) normalization and local bedrock baselines. This multi-faceted approach effectively helped to differentiate basalt subgroups and assess natural concentrations, thereby avoiding misinterpretations of naturally elevated element concentrations as mining-related pollution. Crucially, this work establishes a robust local geochemical baseline for the PEMD area, providing a critical framework for accurate environmental risk assessments and sustainable mineral resource management, and informing national environmental quality standards and remediation efforts in Ecuador. It underscores the necessity of evaluating local geology, including inherent mineralization, when defining environmental baselines and understanding the fate of PTEs in mining-impacted environments. Full article

The new mineral achyrophanite (K,Na)₃(Fe³⁺,Ti,Al,Mg)₅O₂(AsO₄)₅ was found in high-temperature sublimates of the Arsenatnaya fumarole at the Second scoria cone of the Northern Breakthrough of the Great Tolbachik Fissure Eruption, Tolbachik volcano, Kamchatka, Russia. It is associated with aphthitalite-group sulfates, hematite, alluaudite-group arsenates (badalovite, calciojohillerite, johillerite, nickenichite, hatertite, and khrenovite), ozerovaite, pansnerite, arsenatrotitanite, yurmarinite, svabite, tilasite, katiarsite, yurgensonite, As-bearing sanidine, anhydrite, rutile, cassiterite, and pseudobrookite. Achyrophanite occurs as long-prismatic to acicular or, rarer, tabular crystals up to 0.02 × 0.2 × 1.5 mm, which form parallel, radiating, bush-like, or chaotic aggregates up to 3 mm across. It is transparent, straw-yellow to golden yellow, with strong vitreous luster. The mineral is brittle, with (001) perfect cleavage. D_calc is 3.814 g cm^–3. Achyrophanite is optically biaxial (+), α = 1.823(7), β = 1.840(7), γ = 1.895(7) (589 nm), 2V (meas.) = 60(10)°. Chemical composition (wt.%, electron microprobe) is: Na₂O 3.68, K₂O 9.32, CaO 0.38, MgO 1.37, MnO 0.08, CuO 0.82, ZnO 0.48, Al₂O₃ 2.09, Fe₂O₃ 20.42, SiO₂ 0.12, TiO₂ 7.35, P₂O₅ 0.14, V₂O₅ 0.33, As₂O₅ 51.88, SO₃ 1.04, and total 99.40. The empirical formula calculated based on 22 O apfu is Na_1.29K_2.15Ca_0.07Mg_0.34Mn_0.01Cu_0.11Zn_0.06Al_0.44Fe³⁺_2.77Ti_1.00Si_0.02P_0.02S_0.14V_0.04As_4.90O₂₂. Achyrophanite is orthorhombic, space group P222₁, a = 6.5824(2), b = 13.2488(4), c = 10.7613(3) Å, V = 938.48(5) ų and Z = 2. The strongest reflections of the PXRD pattern [d,Å(I)(hkl)] are 5.615(59)(101), 4.174(42)(022), 3.669(31)(130), 3.148(33)(103), 2.852(43)(141), 2.814(100)(042, 202), 2.689(29)(004), and 2.237(28)(152). The crystal structure of achyrophanite (solved from single-crystal XRD data, R = 4.47%) is unique. It is based on the octahedral-tetrahedral M-T-O pseudo-framework (M = Fe³⁺ with admixed Ti, Al, Mg, Na; T = As⁵⁺). Large-cation A sites (A = K, Na) are located in the channels of the pseudo-framework. The achyrophanite structure can be described as stuffed, with the defect heteropolyhedral pseudo-framework derivative of the orthorhombic Fe³⁺AsO₄ archetype. The mineral is named from the Greek άχυρον, straw, and φαίνομαι, to appear, in allusion to its typical straw-yellow color and long prismatic habit of crystals. Full article

The Aghbar-Bou Azzer East mining district (ABED) is located between the Bou Azzer East and Aghbar deposits. It is an area of approximately 7 km long towards ENE–WSW and 2 km wide towards N–S. In this barren area, volcano-sedimentary rocks are attributed to the Ouarzazate group outcrop (Ediacarian age): they are composed of volcanic rocks (ignimbrite, andesite, rhyolite, dacite, etc.) covered by the Adoudou detritic formation in angular unconformity. Given the absence of serpentinite outcrops, exploration investigation in this area has been very limited. This paper aims to use ionic leach geochemistry (on samples of soil) to detect the presence of Co-bearing arsenides above hidden ore deposits in this unexplored area of the Bou Azzer inlier. In addition, a detailed structural analysis allowed the identification of four families of faults and fractures with or without filling. Three directional major fault systems of several kilometers in length and variable orientation in both the Cryogenian basement and the Ediacaran cover have been identified: (i) ENE–WSW, (ii) NE–SW, and (iii) NW–SE. Several geochemical anomalies for Co, As, Ni, Ag, and Cu are aligned along three main directions, including NE–SW, NW–SE, and ENE–WSW. They are particularly well-defined in the western zone but are only minor in the central and eastern zones. Some of these anomalies correlate with the primary structural features observed in the studied area. These trends are consistent with those known under mining exploitation in nearby ore deposits, supporting the potential for similar mineralization in the ABED. Based on structural analysis and ionic leach geochemistry, drilling programs were conducted in the study area, confirming the continuity of serpentinites at depth beneath the Ediacaran cover and the presence of Co–Fe-bearing arsenide ores. This validates the ionic geochemistry technique as a reliable method for exploring buried ore deposits. Full article

The Dulong deposit in Wenshan, southeastern Yunnan Province, is rich in zinc, tin, and copper resources, accompanied by rare metals such as indium and silver. It is a particularly important indium production base, with reserves of approximately 7000 tons, ranking first globally. Enrichment and recovery of indium-bearing minerals are mainly achieved through mineral processing technology. However, the recovery rate of indium in the Dulong concentrator remains relatively low, and there is an insufficient understanding of its occurrence state and distribution characteristics, resulting in marked indium resource wastage. Here, we conducted a systematic process mineralogy study on indium-bearing polymetallic ore in the Dulong concentrator. The average grade of indium in the ore is 43.87 g/t, mainly occurring in marmatite (63.63%), supplemented by that in silicate minerals (23.31%), chalcopyrite (7.84%), and pyrrhotite (4.22%). The indium has a relatively dispersed distribution, which is inconducive to enrichment and recovery. The substitution mechanism of indium in marmatite was investigated using laser ablation inductively coupled plasma mass spectrometry. This revealed a positive correlation between indium and copper, allowing us to revise the substitution relationship to: ${\mathrm{Zn}}_x\mathrm{S}+{\mathrm{Cu}}^{+}+{\mathrm{In}}^{3+}\to {\mathrm{Zn}}_{\mathrm{x}-2}\mathrm{CuInS}+2{\mathrm{Zn}}^{2+}$ or ${\mathrm{Zn}}_{\mathrm{x}-1}\mathrm{FeS}+{\mathrm{Cu}}^{+}+{\mathrm{In}}^{3+}\to {\mathrm{Zn}}_{\mathrm{x}-2}\mathrm{CuInS}+{\mathrm{Zn}}^{2+}+{\mathrm{Fe}}^{2+}$. Electron probe microanalysis revealed the presence of roquesite (CuInS₂), an independent indium mineral not previously reported from this deposit. Our detailed investigation of the Dulong concentrator mineral processing technology showed that the recovery rate of indium from marmatite is currently poor, at only 48.01%. To improve the comprehensive utilization rate of indium resources, it will be necessary to further increase the recovery rate from marmatite and explore the flotation recovery of indium from chalcopyrite and pyrrhotite. Full article

The Carajás Mineral Province hosts one of the world’s most extensive sulfide-bearing copper belts. These deposits are typically covered by thick regolith, including gossans, laterites, colluviums, and soil, which can be used as important exploration indicators. In some cases, these covers can be mined alongside the parent hypogene ore. Therefore, accurate identification of copper-bearing minerals is essential for selecting the most appropriate metallurgical techniques. This study investigated the saprolite horizon overlying the Alvo 118 deposit, where the parent rocks are chloritites hosting copper-bearing hypogene sulfides, partially altered to an immature gossan. Saprolite formation was primarily controlled by the weathering of chlorite, mostly converted into kaolinite, with smectite and vermiculite serving as intermediates, forming a typical lower saprolite association. During weathering, iron released from chlorite and indirectly by vermiculite and smectite contributed to the formation of ferrihydrite, goethite, and hematite. Magnetite octahedrons, relics of the hypogene ore, pseudomorphic phases, are embedded in the clay mineral matrix. While FTIR analysis of kaolinite showed no evidence of copper retention, Mössbauer spectroscopy enabled the quantification of iron-bearing minerals, revealing a strong correlation between CuO contents and goethite and ferrihydrite. These results suggest that goethite and ferrihydrite may be the main copper carriers in the deposit, consistent with findings from similar deposits. Weak acid leaching is proposed as the most effective technique for copper extraction from this mineralization type. Full article

The Shuixie Cu–Co polymetallic orefield, located in western Yunnan Province (southeastern margin of the Qinghai–Tibet Plateau), is renowned for its Cu–Co mineralization. A recent resource reassessment identified Sb–Au and Cu–Co–Bi (Sb–Au) orebodies as genetically associated with primary Cu–Co mineralization. The mineralization characteristics and microscopic observations indicate that gold mineralization in the Sb–Au orebodies follow a pulsating fluid injection model. The model includes four pulses: (1) euhedral gold-poor pyrite (PyI₁) precipitation; (2) margin-parallel growth of gold-rich pyrite (PyI₂) on PyI₁; (3) continued growth of gold-rich pyrite (PyI₃) along PyI₂; and (4) outermost concentric gold-rich pyrite (PyI₄) formation. This study examined gold-bearing pyrite in orebodies and host rocks. In situ laser ablation inductively coupled plasma mass spectrometry (LA–ICP–MS) analysis of pyrite and inductively coupled plasma mass spectrometry (ICP–MS) whole-rock trace element analysis were conducted to track the ore-forming fluid evolution. Compared with CI chondrite, pyrites from all pulses were enriched in LREEs over HREEs. The pyrite REE distribution curves exhibited right-skewed patterns, reflecting LREE enrichment. The Hf/Sm, Nb/La, and Th/La ratios were generally below 1, indicating high-field-strength element depletion. These results suggest a Cl-rich, F-poor ore-forming fluid. The pyrite trace elements showed enrichment in the chalcophile elements (e.g., Cu and Pb) and exceptionally high Bi levels compared with the continental crust. The chalcophile elements (e.g., Zn and Cd) were depleted, whereas iron-group elements (e.g., Co) were enriched and Ni was depleted. The pyrite δCe values (0.87–1.28, mean = 1.01) showed weak anomalies, indicating a reducing ore-forming environment. The δEu values of pyrite during pulses 1 to 4 ranged widely, from 0.2–3.01 (mean of 1.17), 0.27–1.39 (0.6), and 0.41–1.40 (0.96) to 0.4–1.36 (0.84), respectively, suggesting an initial temperature decline and subsequent increase in the ore-forming fluid. Significant variations were found in the Y/Ho, Zr/Hf, and Nb/Ta ratios across pulses, indicating the potential involvement of high-temperature hydrothermal fluids or late-stage alteration during ore formation. The Y/Ho ratio of pyrite overlapped most closely with that of the continental crust of China, indicating a close relationship between the ore-forming fluids and the crust. Full article

Typical greisen-type ore samples from northeastern Tasmania were investigated for their critical metal potential. The samples contain zinnwaldite (KLiFe²⁺Al(AlSi₃O₁₀)(F,OH)₂), a lithium-bearing mica that is prone to excessive breakage during conventional processing, leading to the generation of very-fine-sized particles (i.e., slimes, <20 µm), eventually ending up in tailings and resulting in lithium (Li) loss. To assess whether the natural grain size of valuable minerals could be preserved, the samples were processed using electric pulse fragmentation (EPF). The results indicate that EPF preferentially fragmented along mica-rich veins, maintaining coarse grain sizes, although a lower degree of liberation was observed in fine-grained, massive samples. In addition, the critical metal distribution within zinnwaldite was examined using laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS) techniques. The results reveal differences in Li content between groundmass zinnwaldite and vein-hosted zinnwaldite and that the zinnwaldite contains the critical elements rubidium (Rb), cesium (Cs), and rare earth elements (REEs: La, Ce, Pr, and Nd). Vein-hosted zinnwaldite has a higher average Li content, whereas groundmass mica contains higher concentrations of Rb, Cs, and REEs. Both mica types host inclusions of bismuth–copper–thorium–arsenic (Bi-Cu-Th-As), which are more abundant in vein-hosted mica. In some of the samples, Bi, Cu, Th, and REEs also occur along the mica cleavage planes, as well as in mineral inclusions. The Li, Rb, and Cs grades are comparable to those of European deposits, such as Cínovec and the Zinnwald Lithium Project. Full article

The dispersed elements Ga, Ge, and In are crucial strategic mineral resources often enriched in Pb-Zn deposits. The Chipu Pb-Zn deposit, located on the western edge of the Yangtze Block, lies to the north of the Sichuan-Yunnan-Guizhou (SYG) Pb-Zn metallogenic province with large amounts of Emeishan basalt. Based on trace element and in situ sulfur isotope analyses by (LA)-ICP-MS, sphalerite is the main carrier mineral for Ga (17~420 ppm), Ge (3.87~444 ppm), and In (31~720 ppm). Ga or Ge correlate significantly with Cu, while In substitutes for Zn in sphalerite alongside Fe. Key substitution reactions include Ga³⁺ + Cu⁺ ↔ 2Zn²⁺, Ge⁴⁺ + 2Cu⁺ ↔ 3Zn²⁺, and 2In³⁺ + Fe²⁺ ↔ 4Zn²⁺. Sphalerite crystallized at medium to low temperatures (114–195 °C). Sulfide δ³⁴S values (+3.48 to +24.74‰) suggest sulfur mainly originated from Dengying Formation marine sulfates via thermochemical sulfate reduction (TSR). Metal-bearing fluid release at 30 Ma post-Emeishan mantle plume activity (261–257 Ma) coincides with the Chipu deposit’s mineralization period (230–200 Ma), suggesting the Chipu deposit is associated with Emeishan plume activity. The magmatic activity drove basinal brine circulation, extracting In from intermediate-felsic igneous rocks and metamorphic basement. Elevated temperatures promoted the coupling of Fe and In into sphalerite, causing anomalous In enrichment. Full article

The growing demand for green and, therefore, sustainable technologies present new challenges for our society. The European Union (EU) identified the critical raw materials (CRMs) and strategic raw materials (SRMs) necessary for these technologies and introduced policies to reduce reliance on external suppliers, which includes investigating the recovery of CRMs from extractive waste. This study assesses the recovery potential of mine waste collected in the Traversella mine district (Piedmont, Italy), known for its polymetallic Fe-Cu-W deposit. The characterization of waste rock samples involved chemical and mineralogical analyses, revealing metallic-bearing minerals such as magnetite and scheelite. Laboratory-scale magnetic and gravity separation tests were carried out and compared. Magnetic separation resulted in a recovery of 75.4% of Fe, 72.3% of Cu, and 83.7% of W, with a weak concentration. Instead, gravity separation produced high-grade Fe (67.6%) and W (1289 ppm) concentrate with lower recovery rates. Full article

Critical metals in coal-bearing strata have recently emerged as a frontier hotspot in both coal geology and ore deposit research. In the Upper Carboniferous coal-bearing “Si–Al–Fe” strata (Benxi Formation) of the North China Craton (NCC), several critical metals, including Li, Ga, Sc, V, and rare earth elements and Y (REY or REE + Y), have been discovered, with notable mineralization anomalies observed across northern, central, and southern Shanxi Province. However, despite the widespread occurrence of outcrops of the “Si–Al–Fe” strata in the northeastern Qinshui Basin of eastern Shanxi, there has been no prior report on the critical metal content in this region. Traditionally, the “Si–Al–Fe” strata have been regarded as a primary source of clastic material for the surrounding coal seams of the Carboniferous–Permian Taiyuan and Shanxi Formations, which are known to display critical metal anomalies (e.g., Li and Ga). Given these observations, it is hypothesized that the “Si–Al–Fe” strata in the northeastern Qinshui Basin may also contain critical metal mineralization. To evaluate this hypothesis, new outcrop samples from the “Si–Al–Fe” strata of the Benxi Formation in the Yangquan area of the northeastern Qinshui Basin were collected. Detailed studies on critical metal enrichment were assessed using petrographic observations, mineralogy (XRD, X-ray diffractometer), and geochemistry (XRF, X-ray fluorescence spectrometer, and ICP-MS, inductively coupled plasma mass spectrometer). The results indicate that the siliceous, ferruginous, and aluminous rocks within the study strata exhibit varying degrees of critical metal mineralization, mainly consisting of Li and REY, with minor associated Nb, Zr, and Ga. The Al₂O₃/TiO₂, Nb/Y vs. Zr/TiO₂, and Nb/Yb vs. Al₂O₃/TiO₂ diagrams suggest that these critical metal-enriched layers likely have a mixed origin, comprising both intermediate–felsic magmatic rocks and metamorphic rocks derived from the NCC, as well as alkaline volcaniclastics associated with the Tarim Large Igneous Province (TLIP). Furthermore, combined geochemical parameters, such as the CIA (chemical index of alteration), Sr/Cu vs. Ga/Rb, Th/U, and Ni/Co vs. V/(V + Ni), indicate that the “Si–Al–Fe” strata in the northeastern Qinshui Basin were deposited under warm-to-hot, humid climate conditions, likely in suboxic-to-anoxic environments. Additionally, an economic evaluation suggests that the “Si–Al–Fe” strata in the northeastern Qinshui Basin hold considerable potential as a resource for the industrial extraction of Li, REY, Nb, Zr, and Ga. Full article

The Yidun island arc was formed in response to the Late Triassic westward subduction of the Ganzi–Litang oceanic plate, a branch of the Paleo-Tethys Ocean. The Zhongdian arc, located in the south of the Yidun island arc, has relatively large number of porphyry (skarn) type Cu–Mo ± Au polymetallic deposits, the largest of which is the Pulang Cu (–Mo–Au) deposit with proven Cu reserves of 5.11 Mt, Au reserves of 113 t, and 0.17 Mt of molybdenum. However, the relationship between mineralization and the potassic alteration zone, phyllic zone, and propylitic zone of the Pulang porphyry deposit is still controversial and needs further study. Titanite (CaTiSiO₅) is a common accessory mineral in acidic, intermediate, and alkaline igneous rocks. It is widely developed in various types of metamorphic rocks, hydrothermally altered rocks, and a few sedimentary rocks. It is a dominant Mo-bearing phase in igneous rocks and contains abundant rare earth elements and high-field-strength elements. As an effective geochronometer, thermobarometer, oxybarometer, and metallogenic potential indicator mineral, titanite is ideal to reveal the magmatic–hydrothermal evolution and the mechanism of metal enrichment and precipitation. In this paper, major and trace element contents of the titanite grains from different alteration zones were obtained using electron probe microanalysis (EPMA) and laser-ablation inductively coupled plasma mass spectrometry (LA-ICP-MS) to define the changes in physicochemical conditions and the behavior of these elements during the process of hydrothermal alteration at Pulang. Titanite in the potassic alteration zone is usually shaped like an envelope. It occurs discretely or is enclosed by feldspar, with lower contents of CaO, Al, Sr, Zr and Hf; a low Nb/Ta ratio; high ∑REE + Y, U, Th, Ta, Nb, and Ga content; and high FeO/Al₂O₃ and LREE/HREE ratios. This is consistent with the characteristics of magmatic titanite from fresh quartz monzonite porphyry in Pulang and other porphyry Cu deposits. Titanite in the potassium silicate alteration zone has more negative Eu anomaly and a higher U content and Th/U ratio, indicating that the oxygen fugacity decreased during the transformation to phyllic alteration and propylitic alteration in Pulang. High oxygen fugacity is favorable for the enrichment of copper, gold, and other metallogenic elements. Therefore, the enrichment of copper is more closely related to the potassium silicate alteration. The molybdenum content of titanite in the potassium silicate alteration zone is 10²–10⁴ times that of the phyllic alteration zone and propylitic alteration zone, while the copper content is indistinctive, indicating that molybdenum was dissolved into the fluid or deposited in the form of sulfide before the medium- to low-temperature hydrothermal alteration, which may lead to the further separation and deposition of copper and molybdenum. Full article

Due to the gradual depletion of traditional metallic mineral resources, the search for new potential sources is an important issue. One such source is coal deposits. The extraction of metals from coal is a way to produce clean energy. This study presents the results of detailed research on geochemical features and mineralogy to understand the processes of microelement enrichment in the coal-bearing deposit of Shubarkol, in Central Kazakhstan. Modern analytical techniques were used to obtain information about the conditions and processes of trace element accumulation in coal, as well as the modes of occurrence of these elements. Geochemical data were analyzed using multidimensional statistical methods, including correlation, clustering, and factor analysis, which allowed us to draw several scientific conclusions. Numerous factors indicate that the enrichment of trace elements in sediments is controlled by clastic terrigenous material and low-temperature hydrothermal solutions circulating in the coal basin. The main sources of removal of trace elements from coal are ancient igneous rock complexes located within deposits that were directly involved in coal enrichment through secondary geological processes. According to estimates, the degree of enrichment of Jurassic coals at Shubarkol was close to the average value for world coals (0.5 < CC < 2), and coal seams were enriched with lithophilic and chalcophilic elements such as Ba, U, Yb, Co, La, Nb, Hf, Sc, V, Sr, Cu, and Zn. A correlation analysis of coal deposits revealed a significant correlation between main oxides and rare earth elements (REEs). The strongest correlation was between Zr, Hf, Th/Ta, and REEs. The positive correlations between Zr and Al₂O₃, Nb and Al₂O₃ indicate that these elements (Zr, Hf, Nb, Ta, and REY) are probably related to Al. The results obtained make it possible to consider coal as a potential mineral resource for the production of rare metals and serve as a guide for the industrial processing of the most important elements found in coal. Full article