Ore Deposits Research Articles

Iron-rich Ca[sbnd]Mg skarns from the SW East European Craton (Lithuania): Microstructural study, mineral reactions and direct age constraints of ore-forming events using LA-ICPMS

The Varena Iron Ore deposit in the SW East European Craton is a significant ore body that occurs within metamorphosed and hydrothermally reworked Paleoproterozoic dolostones. We have performed microstructural investigations supplemented with mineral chemistry and geochronological investigations (LA-ICP-MS) to obtain age constraints on the ore-forming event(s) and improve the understanding of the conditions during mineralization process. Mineral chemistry and textures suggest a drop in pressure after the event of peak metamorphic skarn formation. Influx of oxidized, iron-rich H2O fluids resulted in (1) Mg mobility that caused secondary dolomitization of calcite, (2) dissolution of metamorphic magnetite and formation of a new, inclusion-rich (Mag-1) and inclusion-poor (Mag-2) magnetite, and (3) replacement of the peak skarn assemblages. During these fluid-related processes, accessory phases of monazite, baddeleyite, and zircon were formed. Their UPb dating yield individually robust ages of 1721 ± 9 Ma (monazite, 23 spots), 1703 ± 10 Ma (baddeleyite, 18 spots) and 1706 ± 54 Ma (zircon, 14 spots), respectively. The weighted mean age of 1713 ± 7 Ma (2σ internal) is considered to represent the best age estimate of the iron-ore mineralization in the Varena Iron Ore deposit, and possibly also dates influx of P, REEs etc. into the system. This mineralization event is contemporaneous with ca. 1.73–1.70 Ga metamorphic reworking of the host rocks in the region and may be linked to regional continental-margin type Transscandinavian Igneous Belt (TIB) magmatism in south-central Sweden.

Mineral Prospectivity Mapping Based on Spatial Feature Classification with Geological Map Knowledge Graph Embedding: Case Study of Gold Ore Prediction at Wulonggou, Qinghai Province (Western China)

AbstractProspectivity mapping based on deep learning typically requires substantial amounts of geological feature information from known mineral deposits. Due to the limited spatial distribution of ore deposits, the training of predictive models is often hampered by insufficient positive samples. Meanwhile, data-driven mineral prospectivity mapping often overlooks domain knowledge and expert experience, leading to poor interpretability of predictive results. To address this problem, we employed the Gaussian mixture model (GMM) for spatial feature classification to expand the number of positive samples. The approach integrated the embedding of geological map knowledge graphs with geological exploration data to enhance the knowledge constraints of the prospecting model, which enabled the integration of knowledge with data. Considering the complex spatial structure of geological elements, a bi-branch utilizing the 1-dimensional convolutional neural network (CNN1D) and graph convolutional network (GCN) was used to extract geological spatial features for model training and prediction. To validate the effectiveness of the method, a gold mineralization prediction study was conducted in the Wulonggou area (Qinghai province, western China). The results indicate that, when the number of GMM spatial feature classifications was 17, the positive-to-negative sample ratio was optimal, and the embedding of the knowledge graph controlled the prediction area distribution effectively, which demonstrated strong consistency between the prospecting area and the known mineral deposits. Compared with the predictions by CNN1D, the fused prediction model of CNN1D and GCN yielded higher accuracy. Our model identified 11 classes of mineralization potential areas and provides geological interpretations for different prediction categories.

A billion-year shift in the formation of Earth’s largest ore deposits

Banded iron formations (BIFs) archive the relationship between Earth's lithosphere, hydrosphere, and atmosphere through time. However, constraints on the origin of Earth's largest ore deposits, hosted by BIFs, are limited by the absence of direct geochronology. Without this temporal context, genetic models cannot be correlated with tectono-thermal and atmospheric drivers responsible for BIF upgrading through time. Utilizing in situ iron oxide U-Pb geochronology, we provide a direct timeline of events tracing development of all the giant BIF-hosted hematite deposits of the Hamersley Province (Pilbara Craton, Western Australia). Direct dating demonstrates that the major iron ore deposits in the region formed during 1.4 to 1.1 Ga. This is one billion to hundreds of millions of years later than previous age constraints based upon 1) the presence of hematite ore clasts in conglomerate beds deposited before ~1.84 Ga, and 2) phosphate mineral dating, which placed the onset of iron mineralization in the Province at ~2.2 to 2.0 Ga during the great oxidation event. Dating of the hematite clasts verified the occurrence of a ~2.2 to 2.0 Ga event, reflecting widespread, but now largely eroded iron mineralization occurring when the Pilbara and Kaapvaal cratons were proximal. No existing phosphate mineral dates overlap with obtained hematite dates and therefore cannot be related to hematite crystallization and ore formation. New geochronology conclusively links all major preserved hematite deposits to a far younger (1.4 to 1.1 Ga) formation period, correlated with the amalgamation of Australia following breakup of the Columbia supercontinent.

Technogenic gold deposits of the Trans-Baikal Territory

Relevance. The need to expand the mineral resource base of the Trans-Baikal Territory. Aim. To study the geochemical composition of technozems of tailings dumps of gold deposits of the Trans-Baikal Territory, their correspondence, in terms of gold content, to technogenic deposits, to calculate the exceeding the maximum permissible concentrations of toxic elements in technozems of tailings dumps. Objects. Technozems of tailings dumps of gold deposits of the Trans-Baikal Territory. Methods. Silicate, X-ray fluorescence ISP-AES methods in analytical laboratories of the Geological Institute of the SB RAS (Ulan-Ude) and JSC "SGS Vostok Limited" (Chita). Results. It was found that in terms of gold content (Au>0.4 g/t), the technozems of the tailings of the gold deposits of the Trans-Baikal Territory, in general, correspond to technogenic gold deposits. The largest volumes and contents of gold (1.2 g/t) are characterized by technozems of the Baleysky tailings dam deposits with insignificant gold contents are technozems of Darasunsky (0.36 g/t) and Kariysky (0.35 g/t) deposits. It is determined that the chemical composition of the technozems of the tailings depends on the composition of the host rocks developed in the areas of deposits. They correspond to the rocks of both basic and medium compositions. The distinctive features of the content of impurity elements in the technozems of tailings are due to the different compositions of the initial ores of gold deposits. These differences are reflected in the values of exceeding the maximum permissible concentrations relative to soils. Among the toxic elements, arsenic is characterized by maximum exceedances of the maximum permissible concentrations. In the technozems of the Lyubavinsky deposit, the excess of the maximum permissible concentrations of arsenic relative to the soil is 933 times, and the Baley deposit is 397 times.

Lithium capacity of Kazakhstan mineral resource base

Relevance. Weak knowledge of the territory of the Republic of Kazakhstan on lithium raw materials previously mined in the East Kazakhstan region. Aim. To study lithium raw material base in the Republic of Kazakhstan and prospects for the extraction of lithium raw materials. Methods. Content analysis of all information on the subject of the mineral resource base of lithium in the Republic of Kazakhstan. Results. Within the Republic of Kazakhstan, ore deposits of scapolite pegmatites and lithium-bearing greisens-hydrothermal growths are known along alkaline granites. Residual lithium reserves from previously developed rare metal deposits that are equivalent to 36.3 thousand tons of Li2O, predicted resources of known lithium occurrences are estimated at 140 thousand tons of Li2O. It is possible to develop known rare metal deposits with the extraction of tantalum, niobium, beryllium and associated extraction of spodumene concentrate. GRK «Ognevsky Mining and Processing Plant» is already planning to put back to mining of tantalum and beryl (with the associated extraction of spodumene concentrate – up to 2.5 thousand tons/year) at the Bakennoe deposit and processing the resulting ore concentrates at the operating Ulba metallurgical plant of Kazatomprom. With regard to lithium-bearing hydro-mineral resources of the Republic of Kazakhstan, the situation is more complicated, due to the data limitations on the completeness of formation water testing and the reliability of data on surface waters of stagnant lakes. Such oil and gas fields as Karachaganak (up to 196 mg/l Li2O), Kolkuduk (up to 130 mg/l Li2O), Teplovskoe (up to 82.5 mg/l), Urikhtau (up to 52 mg/l) and Western Opak (up to 45 mg/l) are known for high concentration of lithium in formation waters. First two deposits are ready for oil and gas development and production with an annual extraction of up to 1 thousand tons of lithium carbonate. With regard to the lithium content of stagnant lakes of the Republic of Kazakhstan, it should be noted almost total lack of reliable information on sampling their surface waters. Given the fact of finding industrially significant lithium-bearing hydro-mineral lake deposits in adjacent regions of China and Mongolia, it is necessary to intensify the thematic works to assess the lithium content of endorheic lakes throughout the Republic of Kazakhstan, with sampling not only of surface waters, but also of natural brine, lake mud, saline clayey rocks of solonchaks and takyrs.

Compound criticality of bauxite production: implications for sustainability and trade neo-colonialism

We describe bauxite as having compound criticality. (1) It is a critical raw material (CRM) from which alumina and thereby aluminium are produced, and aluminium has the highest production levels of all metals deemed significant to the Clean Energy Transition. (2) Gallium is a by-product CRM, extracted during alumina refining. (3) Multiple other CRM by-products could be extracted during alumina refining: scandium, lithium, cobalt, titanium and REE. (4) Production is profoundly influenced by price inelasticity (for by-products), regime instability of bauxite production and supply chain bottlenecks. We review the geology of bauxite ore deposits as a function of complex CRM supply potential, and interrogate the trait of criticality using four of the world's dominant producer nations of bauxite and potential patterns of value addition from raw materials to refined products. Trade agreements and mitigation strategies to ensure security of supply in consumer regions prioritize removal of low-cost bauxite by large-scale mining operations and shipping of unprocessed ore at high CO 2 footprint from producer nations. Ore-refining nations have investments that are deemed extractive because they remove large quantities of raw material for export with minimal or no in-country processing and they can also place producer nations in debt. Opposition to neo-colonial debt-trap policies and extractive practices increases regime instability and thereby criticality. We highlight how societal-environmental-political interactions and the mineral-energy nexus in the bauxite-aluminium supply chain are subject to increasing turbulence, which may reshape the geographies of supply chains.

Dual-mineralization in the intracontinental Jiangnan Orogen, South China: Evidence from textures and in-situ trace elements and oxygen analysis of quartz from the Woxi Au-Sb-W deposit

The Jiangnan Orogenic Belt (JOB), situated in the interior of the South China Block (SCB), harbors numerous gold-polymetallic deposits, but the ore genesis has been a long-standing controversy. This study examines the Woxi super-large gold deposit in the middle JOB, which is characterized by simultaneous large-scale antimony-tungsten mineralization. The investigation shows that the Woxi ore deposit have developed multiple-stage quartz, i.e., Qz1 (early quartz-carbonate, stage I), Qz2 (quartz-wolframite-scheelite, stage II), Qz3a (quartz-gold-pyrite, early stage III), Qz3b (quartz-stibnite-scheelite, late stage III) and Qz4 (late quartz-carbonate, stage IV). We conducted SEM-CL texture imaging, LA-ICP-MS trace element, and SIMS oxygen isotope analysis on the quartz samples from the main mineralization stages (mainly Qz2 and Qz3). The results reveal a dual mineralization process of the Woxi gold-antimony-tungsten deposit. In the initial stage, the quartz (Qz2) exhibits intense brightness in CL imaging and spiderweb-like texture, shows high concentrations of trace elements, especially Ge, Al and Ti, and has δ18Ofluid values ranging from 10.84 ‰ to 11.64 ‰. These characters are consistent with a magmatic fluid that is acidic (pH<3), reducing, and of relatively high-temperature. In the second stage, the quartz (including Qz3a, Qz3b and Qz4) shows relatively darker CL image and band texture or cobweb mosaic coexistence texture, low concentrations of trace elements, especially Al and Ti, and a low δ18Ofluid values (8.01 ‰ to 9.19 ‰ for Qz3a and 5.83 ‰ to 6.51 ‰ for Qz3b) consistent with characteristics of mantle-derived fluids. The results of this study supports an “intracontinental reactivation metallogenic model”, in which the gold-polymetallic deposits in the JOB formed from a dual-stage mineralization related to tectono-magmatic activities in a back-arc setting. The dual ore-forming processes revealed in this study provide important insights for a comprehensive understanding of the gold-polymetallic deposits in the JOB, and it may be a significant mechanism in the formation of large to super-large gold-polymetallic deposits in this region, which is indicative perspective for exploration of the gold-polymetal deposits. Our work also demonstrates that quartz is an effective tool for identifying the mineralization in the JOB.

Study on fluid inclusions and stable isotopics of W–Mo ore deposits in the Ningshan–Zhen’an area, South Qinling, China

The study of the fluid inclusions of W–Mo deposits in the mineralization area of Ningshan–Zhen’an , Shaanxi Province, China shows that the gas–liquid two-phase inclusions are mainly present in W–Mo deposits, and the ore-forming fluid can be divided into four types: high-temperature type, middle–high-temperature type, middle-temperature type and low-temperature type. The formation depths of the W–Mo mineralization range from 4.2 to 8.4 km. The boiling and mixing of fluid may have been important mechanisms for the formation of W–Mo mineralization. The skarn-type mineralization is dominated by magmatic water, the quartz-vein-type mineralization includes both magmatic water and meteoric water, and the meteoric water is more involved in the quartz-fluorite-vein-type, beryl-quartz-vein-type and pegmatite-type mineralization. Magma is the main source of sulfur; that is, magma is the main source of mineralization. Combined with the metallogenic setting and geological characteristics of typical ore deposits, in the process of structural system transformation in South Qinling, the ore-forming magma fluid in the Late Indosinian–Yanshanian period was uplifted and emplaced along the NW–WNW direction and NE–NNE direction, and eventually, NW–WNW fault-controlled skarn-type W–Mo mineralization and quartz-vein-type W–Mo deposits accompanied by greisenization, albitization and potash feldspathization formed.

Critical Raw Materials Supply: Challenges and Potentialities to Exploit Rare Earth Elements from Siliceous Stones and Extractive Waste

Critical raw materials (CRMs) supply is a challenge that EU countries have to face, with many thinking about domestic procurement from natural ore deposits and anthropogenic deposits (landfills and extractive waste facilities). The present research focuses on the possibilities linked to the supply of CRMs and the potential for exploiting rare earth elements (REEs), investigating a large variety of extractive waste and siliceous rocks in the Piedmont region (Northern Italy). Indeed, the recovery of REEs from the extractive waste (EW) of siliceous quarries and other siliceous ore deposits can be a valuable way to reduce supply chain risks. Starting with a review of the literature on mining activities in Piedmont and continuing with the sampling and geochemical, mineralogical, petrographic, and environmental characterization of EW facilities connected to siliceous dimension stones, of kaolinitic gneiss ore deposits, and of soils present near the investigated areas, this study shows that the degree of REEs enrichment differs depending on the sampling area (soil or EW) and lithology. The concentration of REEs in the EW at some sampling sites fulfils the indicators of industrial-grade and industrial recovery; the high cumulative production and potential market values of EW and the positive recovery effects through proven methodologies indicate a viable prospect of REE recovery from EW. However, REE recovery industrialization faces challenges such as the difficulty in achieving efficient large-scale recovery due to large regional differences in REE abundance, the mismatch between potential market value and waste annual production, etc. Nonetheless, in the future, EW from dimension stone quarries could be differentially studied and reused based on the enrichment and distribution characteristics of trace elements. The present paper shows investigation procedures undertaken to determine both CRMs potentialities and environmental issues (on the basis of literature data employed to select the more-promising areas and on sampling and characterization activities in the selected areas), together with procedures to determine the waste quantities and tentative economic values of REEs present in the investigated areas. This approach, tested on a large area (Piedmont region), is replicable and applicable to other similar case studies (at EU and non-EU levels) and offers decision makers the possibility to acquire a general overview of the potential available resources in order to decide whether and where to concentrate efforts (including economic ones) in a more detailed study to evaluate the exploitable anthropogenic deposits.

Kinetics study on the temperature-dependent reduction of aqueous U(VI) by natural pyrite

Previous studies have indicated that acid-washed pyrite is inert toward aqueous U(VI) under most pH conditions at ambient temperature, even though insoluble UO2 is the thermodynamically predicted product for the reduction of U(VI) by pyrite. Considering the exothermic nature of nuclear waste, the interaction between uranyl nitrate/acetate and natural pyrite was studied at temperatures ranging from 25 °C to 85 °C and at pH values between ∼4.0 and ∼9.5, to simulate the scenarios encountered in a high-level radioactive waste repository. The results revealed that the reactivity of pyrite toward aqueous U(VI) significantly increased with rising temperature, and the reaction could be described by a pseudo-first-order kinetic equation. Activation energies were calculated to be 79.4 ± 10.6 and 45.7 ± 3.8 kJ⋅mol−1 for the reduction of uranyl nitrate, and 78.2 ± 5.2 and 42.2 ± 5.8 kJ⋅mol−1 for the reduction of uranyl acetate, at pH values of ∼4.5 and ∼5.0, respectively. These values indicate that the reaction is controlled by the surface chemical processes. In addition, the complete reduction of aqueous U(VI) to UO2 product was first observed for the reactions at pH ∼4.0 to ∼5.5 when the temperature was ≥75 °C. Conversely, non-stoichiometric UO2+x(s) (0 < x ≤ 0.67) was found at lower temperatures within the same pH range, and also at 85 °C with a reaction pH of ∼9.5. Moreover, the ratio of reduced U(IV/V) on pyrite surfaces increased gradually over time, indicating that reaction time played a significant role in the reduction products. The findings are essential not only for the safety assessment of the high-level radioactive waste repository, but also for understanding the metallogenic mechanism of U(IV)-bearing ore deposits under the relevant anaerobic and hydrothermal conditions.

Identification of processes in Cu-ore heap leaching using Cu isotopes and leachate chemistry at Tschudi mine, northern Namibia

Copper isotopic fractionation (in δ65Cu) and leachate characterization were studied in the context of heap leaching at the Tschudi copper mine in northern Namibia. The leached solution is of Mg-SO4 type with high Al and Fe concentrations. The source of Mg and Al in the leachate can be from the alteration of micas such as Mg-bearing muscovite confirmed by X-ray diffraction and scanning electron microscopy; however, the source of Mg cannot be determined with certainty. The principal secondary minerals identified in the leached ore are gypsum and jarosite. The value of pH in leachate is ∼1.21 and the concentration of dissolved Cu, occurring mostly as CuSO40 and Cu2+, is about 2 g/L. In comparison with unleached ore (avg. δ65Cu −1.47 ‰), leached ore exhibits lighter isotopic values (avg. δ65Cu −6.01 ‰) with apparent isotopic fractionation Δ65Culeached ore-unleached ore of about −4.54 ‰. In contrast, there is isotopic enrichment of leachate in heavier 65Cu isotope (leachate δ65Cu 0.34 ‰) with apparent isotopic fractionation Δ65Culeachate-unleached ore value of +1.81 ‰. These results are in good agreement with Cu isotopic fractionation and depletion in heavier 65Cu isotope reported for dissolution experiments in laboratory and groundwater linked to the porphyry copper ore deposits around the world. The leaching of heaps can be considered an analogy of upper part of gossans, but here the supergene enrichment zone is missing due to extremely low pH and oxidizing conditions.

Insights into the indium enrichment of the Ashele VMS Cu-Zn deposit, Altay, NW China

Indium (In) is a critical metal used in the photovoltaic and semiconductor industries, which have exhibited extraordinary growth in demand. Indium is produced as a by-product of mining from different ore deposits (e.g., epithermal, sediment-hosted, and skarn). Volcanogenic massive sulfide (VMS) deposits are an important source of In; however, the mechanism of In enrichment is not fully understood. Here, we combine mineralogy with in situ trace element and S-Pb isotope geochemistry to reveal the enrichment of indium in the Ashele VMS Cu-Zn deposit (1.08 Mt. Cu, 0.43 Mt. Zn) located in Altay, NW China. The Ashele deposit is hosted in the metamorphosed Devonian felsic-bimodal volcanic rocks. This deposit consists of seafloor hydrothermal, metamorphic hydrothermal, and supergene stages. The seafloor hydrothermal stage comprises macro-scale Cu-rich bands (chalcopyrite, pyrite, and minor sphalerite) and Zn-rich bands (sphalerite, pyrite, and minor chalcopyrite). Indium is mainly hosted by chalcopyrite (mean 178 ppm) and sphalerite (mean 214 ppm) and occurs in the lattice. Mineral assemblages and trace element geochemistry suggest that the Cu-rich bands were deposited under high temperatures (> 300–350 °C) and sulfur fugacity (−7.2 to −4.9), whereas the Zn-rich bands were formed under lower temperatures (180–220 °C) and sulfur fugacity (−15.7 to −11.5). The interlayered Cu-rich and Zn-rich bands may reflect the oscillating temperature and sulfur fugacity variations. In situ S isotopic compositions of sulfides cluster within two ranges: 1–3 ‰ and 3–6 ‰, suggesting two endmembers: volcanic origin and reduced seawater sulfate. Pb isotopic ratios are similar to those of the host volcanic rocks, indicating that the metals may be derived from the felsic volcanic system. During metamorphism, the indium may be retained, but Cu contents of sphalerite become more homogeneous. Most In-rich VMS deposits worldwide are hosted by the felsic-dominant system in island arc and back-arc settings. These tectonic settings are conducive to the production of felsic volcanic systems, which are more likely to contain In mineralization. This study highlights the enrichment mechanism of indium in VMS deposits and suggests that the South Altay could become an important source of In.

Slab melting boosts the mantle wedge contribution to Li-rich magmas

The lithium cycling in the supra-subduction mantle wedge is crucial for understanding the generation of Li-rich magmas that may potentially source ore deposition in continental arcs. Here, we look from the mantle source perspective at the geological processes controlling the Li mobility in convergent margins, by characterizing a set of sub-arc mantle xenoliths from the southern Andes (Coyhaique, western Patagonia). The mineral trace element signatures and oxygen fugacity estimates (FMQ > + 3) in some of these peridotite xenoliths record the interaction with arc magmas enriched in fluid-mobile elements originally scavenged by slab dehydration. This subduction-related metasomatism was poorly effective on enhancing the Li inventory of the sub-arc lithospheric mantle, underpinning the inefficiency of slab-derived fluids on mobilizing Li through the mantle wedge. However, major and trace element compositions of mantle minerals in other xenoliths also record transient thermal and chemical anomalies associated with the percolation of slab window-related magmas, which exhibit an “adakite”-type geochemical fingerprint inherited by slab-derived melts produced during ridge subduction and slab window opening event. As these melts percolated through the shallow (7.2–16.8 kbar) and hot (952–1054 °C) lithospheric mantle wedge, they promoted the crystallization of metasomatic clinopyroxene having exceptionally high Li abundances (6–15 ppm). Numerical modeling shows that low degrees (< 10%) of partial melting of this Li-rich and fertile sub-arc lithospheric mantle generates primitive melts having two-fold Li enrichment (~13 ppm) compared with average subduction-zone basalts. Prolonged fractional crystallization of these melts produces extremely Li-enriched silicic rocks, which may stoke the Li inventory of mineralizing fluids in the shallow crust.

Mineralogical and ore-fluid characteristics of the Onto Porphyry-HSE transition in Hu’u district, West Nusa Tenggara, Indonesia

Abstract Onto prospect is located in the eastern part of Sumbawa Island in West Nusa Tenggara Province, Indonesia. The island is situated within the Sunda-Banda magmatic arc, which extends from west to east, consists of volcanic rocks from the early Miocene to the Holocene. Onto is one of the highly potential prospects and holds significant economic value among ore deposits in Indonesia. The aim of this research is to explain the geological setting and determine the genesis of mineralization based on petrographic, ore microscopic, and fluid inclusion analyses. Eight lithological units have been identified, namely early andesites, polymictic diatreme breccia, upper sedimentary package, caping andesite, quartz-phyric andesite sill, early porphyry, early intra-mineral porphyry, and late intra-mineral porphyry. Nine samples were analyzed for petrography to identify the alteration types consisting of illite-smectite, quartz-dickite, residual vuggy quartz, silicic, quartz-alunite, quartz-pyrophyllite±diaspore, potassic, phyllic-chloritic, and propylitic alterations. Additionally, pyrite, chalcopyrite, and covellite are predominantly present in the study area. Meanwhile, native gold is found as an inclusion in covellite and pyrite. From micro thermometric analysis of fluid inclusions in quartz veins associated with multiphase intrusive rocks, it is shown that the homogenization temperature of early porphyry ranges on average from 279°C to 377°C, early inter-mineral porphyry ranges from 263°C to 361°C, and late intra-mineral porphyry ranges from 275°C to 336°C. The salinity level of the measurements ranges from 5.71 to 10.27% by weight NaCl equivalent, with an average of approximately 8.15% by weight NaCl equivalent. The mineralization formation during the early or prograde phase is associated with the EDM vein system with a mineralization set of biotite-magnetite, digenite, chalcocite, and coevellite, type A veins with quartz-sulfides + anhydrite, M veins type associated with quartz-magnetite-chalcopyrite-bornite mineralization, AB veins type associated with quartz-sulfides + anhydrite textures, and B veins type with sulfide centerline characteristics. The mineralization system during the early stage is generally associated with potassic alteration (K-feldspar-magnetite-secondary biotite). Whereas the retrograde phase, the vein system is associated C veins type with sulfide mineralization groups consisting of massive chalcopyrite + quartz with phyllic alteration (quartz-muscovite-chlorite ± dickite), D veins type with quartz-pyrite+chalcopyrite associated with advanced argillic alteration (quartz-alunite-pyrophyllite ± diasporite), E veins representing the epithermal stage associated with minerals such as quartz-carbonates, galena, sphalerite, chalcopyrite, tetrahedrite-tennatite in the alteration stage of kaolinite-illite-smektite-sericite.

Characterization of evolution of reactive transport parameters during leaching process of sandstone uranium ore by combining porosity and lacunarity

During the in-situ leaching process of sandstone uranium ore deposits, the dynamic evolution of reactive transport parameters, including permeability, tortuosity, and specific surface area (SSA), plays a crucial role in solution flow and solute transport. Characterizing the evolution of these parameters is essential for understanding the leaching process. However, the heterogeneous pore structure of sandstone renders porosity alone insufficient to capture changes in these parameters. This study combines porosity and lacunarity to comprehensively characterize these parameters. For this purpose, leaching experiments were conducted on sandstone uranium ore samples, and CT imaging was performed at different leaching time points. The evolution of reactive transport parameters was analyzed by studying cubic subsamples from the images. The results indicate that both porosity and lacunarity are significant factors influencing the reactive transport parameters. However, neither parameter alone adequately characterizes their evolution. In contrast, combining them accurately characterizes the evolution of reactive transport parameters. Porosity reflects pore quantity, while lacunarity represents pore heterogeneity. Combining these measures facilitates a comprehensive understanding of the evolution of reactive transport parameters and the influence of pore microstructure on macroscopic reactive transport parameters. This research provides valuable insights for optimizing the leaching process in sandstone uranium ore deposits.

Enhancing deep orebody prediction and localization through the revelation of geochemical primary halo patterns in drill holes

Geochemical primary halos play a crucial role in mineral exploration as they provide valuable insights into the dispersion of ore materials, identification of concealed deposits, and determination of ore deposit dimensions. The Naruo mining area in the Duolong mineral district, northern Tibet, China well-known for its worldclass porphyry-epithermal Cu–Au deposits is currently chosen as the study area. We employ statistical and nonlinear methods to analyze geochemical data from drill holes. Specifically, R-type cluster analysis is utilized to evaluate element affinity and concentration index, while an improved Grigorian zoning index is employed to delineate the vertical zoning sequence of the primary halo. These methodologies significantly enhance our understanding of element enrichment within geological contexts and greatly contribute to mineral resource evaluation. Based on these results, we have constructed a vertical zonation index model of denudation coefficient tailored to the geological characteristics of mineralization within the study area. This model effectively represents the vertical variation of the ore body. Our findings reveal a decrease in this zoning index towards the central region of deep ore bodies which correlates with deep granodiorite porphyry occurrences. Furthermore, we observe increasing concentrations of Cu, Ag, and Au with depth in specific sections of drill holes indicating promising exploration potential. Supplementary short-wave infrared data suggests the presence of a deep hydrothermal center in drill hole RNZK2404 which tentatively infers concealed porphyry bodies. Notably, the reversal observed at 4200 m on RNZK2404's zoning index hints at a possible hidden ore body at great depths. Finally, three-dimensional visualization techniques effectively illustrate spatial patterns for elements thereby paving way for future endeavors in mineral exploration.

Microbial Mobilization and Reprecipitation of Transition Metals in Waste Rock from an Abandoned Pyrite Mine: Implications for Metal Recovery

Abstract The Pyrite Mines in Sulphide, Ontario are a collection of historic mine workings representing one of more than 6000 abandoned mines in Ontario. Historic mines are receiving renewed interest as potential sources of critical minerals for use in low carbon technologies. This study characterizes waste rock from the Pyrite Mines in the context of metal distribution, microbial activity, bioleaching, and acid mine drainage (AMD) bioremediation for the recovery of metals. Acidophilic Fe-oxidizing bacteria cultured from the waste rock produced schwertmannite [Fe8O8(OH)8−2x(SO4)x·nH2O] and ammoniojarosite [NH4Fe3(SO4)2(OH)6] with similar morphologies to those often observed in acidic sulfidic mine settings. Fe- and S-oxidizing bacteria found naturally in the waste rock were used in waste rock bioleaching column experiments that demonstrated AMD formation and metal mobilization. The columns produced acidic leachates (pH = 1.75) containing dissolved constituents, including sulfur (1577 mg/L), iron (547.7 mg/L), nickel (12.6 mg/L), manganese (7.3 mg/L), copper (2.3 mg/L), zinc (2.0 mg/L), chromium (1.5 mg/L), and titanium (0.7 mg/L). The proportion of metals successfully leached from the waste rock was variable, with leaching efficiencies calculated for nickel (31%), manganese (10.5%), iron (1.5%), chromium (1.4%), and titanium (0.02%). The leachates produced by the bioleaching columns were amended in subsequent bioremediation columns using sulfate reducing bacteria cultured from the mine site. Remediation efficiencies for elements of interest were calculated as cobalt (100%), chromium (100%), copper (100%), iron (90%), titanium (68%), nickel (52%), manganese (52%), and sulfur (43%). Mapping elemental distributions in thin sections from one of the bioleaching columns using synchrotron X-ray fluorescence microscopy revealed the heterogeneity of the waste rock. Iron was observed in both euhedral mineral grains, likely pyrite, and in secondary cements coating grains in the waste rock. Nickel, manganese, and chromium were primarily co-located with the iron. Titanium was primarily co-located with calcium in titanite (CaTiSiO5), making it challenging to target with bioleaching. This study demonstrates the heterogeneous nature of metal distribution in waste rock from this historic mine site. It indicates that successful metal recovery from legacy mine waste will require such materials to be treated as anthropogenic mineral deposits that require “exploration” and characterization much like naturally occurring ore deposits.

Distribution of Manganese Ore Deposit in Sukaagung Village, Tanggamus Regency, Lampung

Abstract Manganese ore deposits are one of the most widely used metal alloys in everyday life. Generally, manganese ore deposits are present as residual deposits along with iron ore at certain pH and Eh conditions. These deposits can come from the chemical weathering of crystalline schist, limestone, and dolomite rocks or earlier manganese deposits. In Lampung, the presence of manganese ore can be found in Sukaagung Village, Tanggamus Regency, but little research has been done to determine the distribution and potential of manganese ore in this area. Therefore, this study aims to determine manganese ore distribution and enrichment process in the study area using field data and petrography. In general, manganese ore deposits in Sukaagung Village are present as veins that fill fractures and nodules. Manganese ore deposits that were present as fracture fillers were found intersecting marble, quartzite, and mica schist of the Complex of Gunungkasih Tak Terpisahkan, tuffaceous siltstone from Menanga Formation, and the lapilli tuff and andesite of the Hulusimpang Formation. These deposits are present in manganese as botryoidal and dendritic forms in rock fractures. Meanwhile, manganese ore deposits in the form of nodules are present in submarine volcanic sedimentary rocks in the Menanga Formation. The presence of manganese ore deposits in the study area is thought to be the result of the leaching of manganese elements from the banded iron formation which is associated with the Permian-Cretaceous magmatism, hydrothermal submarine, and rift basin. The acidic fluid dissolves other elements and leaves manganese ore as an economical mineral. Manganese ore is then carried by subsurface fluids, filling fractures in Paleozoic-Tertiary rocks. Even though the distribution of manganese ore in Sukaagung Village is quite wide, further research is needed to determine the potential and reserves of manganese ore in the study area.

ORIGIN OF VOLCANIC-HOSTED MAGNETITE AT THE LAGUNA DEL MAULE COMPLEX, CHILE: A NEW EXAMPLE OF ANDEAN IRON OXIDE-APATITE MINERALIZATION

Abstract Iron oxide-apatite (IOA) deposits, also known as magnetite-apatite or Kiruna-type deposits, are a major source of iron and potentially of rare earth elements and phosphorus. To date, the youngest representative of this group is the Pleistocene (~2 Ma) El Laco deposit, located in the Andean Cordillera of northern Chile. El Laco is considered a unique type of IOA deposit because of its young age and its volcanic-like features. Here we report the occurrence of similarly young IOA-type mineralization hosted within the Laguna del Maule Volcanic Complex, an unusually large and recent silicic volcanic system in the south-central Andes. We combined field observations and aerial drone images with detailed petrographic observations, electron microprobe analysis (EMPA), and 40Ar/39Ar dating to characterize the magnetite mineralization—named here “Vetas del Maule”—hosted within andesites of the now extinct La Zorra volcano (40Ar/39Ar plateau age of 1.013 ± 0.028 Ma). Five different styles of magnetite mineralization were identified: (1) massive magnetite, (2) pyroxene-actinolite-magnetite veins, (3) magnetite hydrothermal breccias, (4) disseminated magnetite, and (5) pyroxene-actinolite veins with minor magnetite. Field observations and aerial drone imaging, coupled with microtextural and microanalytical data, suggest a predominantly hydrothermal origin for the different types of mineralization. 40Ar/39Ar incremental heating of phlogopite associated with the magnetite mineralization yielded a plateau age of 873.6 ± 30.3 ka, confirming that the emplacement of Vetas del Maule postdated that of the host andesite rocks. Our data support the hypothesis that the magnetite mineralization formed in a volcanic setting from Fe-rich fluids exsolved from a magma at depth. Ultimately, Vetas del Maule provides evidence that volcanic-related IOA mineralization may be more common than previously thought, opening new opportunities of research and exploration for this ore deposit type in active volcanic arcs.

Li-mineralized pegmatite of anatectic origin: Constraints from Li[sbnd]Hf isotopes and geochemical modeling

Pegmatites are important reservoirs of lithium resources. There is an ongoing debate as to whether Li-mineralized pegmatites were generated from evolved granitic systems via extreme differentiation or by direct melting of metasedimentary rocks. The Chinese Altay is one of the largest pegmatite provinces in the world, and includes many rare-metal pegmatites (e.g., Koktokay, Kelumute, Kaluan and Azubai). However, they display significant differences in formation ages and isotopic compositions compared with the neighbouring or potential parental granites. In this contribution, we present a case study of the Kaluan Li ore deposit in the Chinese Altay, elucidating the origins of pegmatites and related Li mineralization. The Kaluan Li-mineralized pegmatites are characterized by high SiO2, K2O, Na2O, Li, Cs, Ta, and Rb contents; low Fe2O3T, MgO, Ba, and Sr contents; and peraluminous signatures. They have homogeneous HfLi isotopic compositions (εHf (t) = −0.6 to +2.5; δ7Li = +1.6 to +5.8‰) that are within the range of HfLi isotopic compositions of the Kulumuti Group schists (εHf (t) = −2.8 to +7.5; δ7Li = −8.6 to +10.8‰). In addition, the chemical compositions of the melt derived from the partial melting of the Kulumuti Group by phase equilibrium modeling are compatible with our analyses of the Kaluan Li-mineralized pegmatites. These similarities suggest that the Kaluan Li-mineralized pegmatites were derived from the partial melting of the Kulumuti Group schists at depths during the Triassic, in a post-orogenic and extensional setting. The generation of these pegmatites was mostly controlled by biotite dehydration melting at relatively high temperatures, rather than by the low-temperature melting of muscovite. Trace elements modeling results show that approximately 33–36% partial melting of the average Kulumuti Group schist may produce melts with maximum Li concentrations ranging from 664 to 751 ppm. Subsequently, a high degree of fractionation exceeding 85%, was required for the Li concentration of the residual melt to reach concentrations suitable for crystallization into albite-spodumene pegmatites. Based on our research, an anatectic origin model may have general applicability in explaining the genesis and mineralization of rare-metal pegmatites in the Chinese Altay.