Styles Of Mineralization Research Articles

The multifractal nature of worldclass orogenic gold systems in greenstone belts: A multiscale approach and case study at the Córrego do Sítio deposit, Rio das Velhas greenstone belt, Brazil

Understanding the controls on the spatial distribution of mineral deposits is crucial for prospecting new occurrences. Various geological processes operate together at microscopic to macroscopic scales, generating mineral systems responsible for significant accumulations of economic minerals. This characteristic of functioning at various scales, accompanied by repetition of features over space during mineralization, indicates that these processes are self-similar, meaning they exhibit fractal geometry. Previous research has demonstrated that the combined action of processes involved in mineralization in such critical, nonlinear systems, produces objects with multifractal characteristics. Therefore, the spatial distribution of mineral deposits should be studied using appropriate methods for better understanding of their controls. In this context, this study investigated the multiscale geometric characteristics of worldclass orogenic gold systems in Archean greenstone belts using fractal and multifractal analyses. First, at the macroscopic-scale, regional-scale features were considered in the major greenstone belt provinces with orogenic gold deposits worldwide, namely: Abitibi (Canada), Norseman–Wiluna (Australia), Rio das Velhas (Brazil), and Central Lapland (Finland). Next, at an intermediate scale, local-scale features were examined in detail within the context of the Córrego do Sítio Lineament. Finally, at the microscopic scale, the focus was on the Córrego do Sítio orogenic gold deposit—a key deposit in the Rio das Velhas greenstone belt. Fractal dimensions of the spatial distributions of mineral deposits, magnetic lineaments, and their intersections were investigated at the macroscopic to local scales, as well as the spatial distribution of ore minerals at the microscopic scale, using the box-counting method. Maps of fractal dimensions of magnetic lineaments were generated and compared with the spatial distribution and tonnage of orogenic gold deposits at the regional scale. The same features were analyzed using the method of multifractal moments. The results at the three scales were analyzed and synthesized to identify meaningful patterns for understanding these orogenic gold systems. With regard to fractality, the orogenic gold deposits in all the investigated provinces exhibited unique spatial distributions at different scales, namely: less than 2–4 km, from 2 to 4 km to 10–30 km, and more than 10–30 km. The analysis of magnetic lineaments yielded a correlation between gradients of fractal dimensions and gold tonnages in the orogenic gold deposits. The multifractal analyses indicate multifractal geometries extending from the microscopic to the macroscopic scale. The calculated multifractal indices of Δα (singularity variation), τ“(1) (multifractality index), and Δf(α) (multifractal spectrum variation) showed direct relationships with endowment of orogenic gold in the studied provinces, as well as with differences in mineralization styles in thin sections. The findings demonstrate the effectiveness of the analyses used for improved characterization of the studied mineral systems; they also allow comparing similar systems at different scales and locations and they can be used to study other mineral systems with similar geological controls.

Hydrothermal Mineralization and Mineral Chemistry of Arsenides and Sulfarsenides in the Fe-Co-Ni-As-S System and Introduction of Three Unique Minerals, Port Radium Deposit, Canada

The Port Radium U-Cu-Ni-Co-Ag deposit in northwestern Canada is hosted within a mineral system that has generated a variety of mineralization styles from iron oxide-copper-gold to iron oxide-apatite, porphyry, skarn, and epithermal. Their genesis is linked to an extensive subduction-related magmatism that formed widespread dacite-rhyodacite-andesite volcanic and volcanoclastic sequences (~1.87 Ga), which have been intruded by their equivalent intrusive plutons. Pervasive and intensive hydrothermal alterations, including albitic, magnetite-actinolite-apatite, potassic ± albitic, phyllic, and propylitic occurred before the main sulfide, sulfarsenide, and uraninite vein-type mineralization. Although scarce sulfide minerals formed at the beginning of the hydrothermal activity, the main polymetallic arsenide-sulfarsenide-sulfide ± uraninite vein-type mineralization occurred during the epithermal stage. In addition to the common arsenides and sulfarsenides including nickeline, cobaltite, rammelsbergite, safflorite, skutterudite, gersdorffite, and arsenopyrite, three unique sulfarsenides were also found: Co0.67Ni0.32Fe0.02S0.19As2.80, which could be a sulfur-rich skutterudite, Ni0.85Co0.15S0.39As1.60, and Ni0.69Co0.31S0.47As1.52, which are chemically comparable to the Port Radium rammelsbergite with substantial addition of S and Co; they could be the solid solution product of gersdorffite-cobaltite or safflorite-rammelsbergite.

Characteristics of Gold and Its Mineralization Style in the Boulon Djounga Eastern Perimeter of Liptako Mining Company (Central Southwestern Niger)

Characteristics of Gold and Its Mineralization Style in the Boulon Djounga Eastern Perimeter of Liptako Mining Company (Central Southwestern Niger)

Growth and Stability of Stratiform Carrollite (CuCo2S4) in the Tenke-Fungurume Ore District, Central African Copperbelt

Abstract Carrollite (CuCo2S4) is the main ore mineral of the critical battery metal cobalt, yet, surprisingly, detailed characterization of its thermodynamic properties and of its trace element contents remain sparse in the scientific literature. To fill these knowledge gaps, we generated the first thermodynamic data set for carrollite using well-characterized samples obtained from the stratiform sulfide mineralization style at Fungurume 88 deposit in the Democratic Republic of Congo. Detailed mineralogical investigation of these same samples suggests that carrollite has limited ability to incorporate other ‘sweetener’ elements (except Cu and Ni) by substitution mechanisms. Modeling using CHNOSZ 2.0.0. software and an integrated Cu-Co-S-O thermodynamic data set provides insights into the stability of carrollite relative to other Co-bearing minerals under physicochemical conditions relevant to the Central African Copperbelt. Further exploration of these models indicates that dropping redox potential in the mineralizing system is insufficient to explain the mineral-scale and deposit-scale zonation patterns commonly observed in Cu-Co deposits of the Central African Copperbelt. Instead, factors such as increasing pH, decreasing T, decreasing sulfur activity, or some combination of changing physicochemical parameters may need to be invoked to explain these zonation trends. At the Fungurume 88 deposit, the absence of linnaeite (Co3S4) suggests that ore precipitation occurred at temperatures cooler than 211 °C. From our pH-logfO2 diagrams, and relative to higher temperatures, such a lower T regime is marked by a greater degree of offset between the modeled Cu and Co solubility contours, thus facilitating a more differentiated and zoned distribution of these two metals at the deposit scale. Our models are offered to the geoscience community as exceptionally useful tools for modeling and visualizing the Cu-Co-S-O systematics and may be applied to a variety of geological and geometallurgical questions in the Central African Copperbelt and other deposits elsewhere.

Permian−Triassic magmatism above a slab window in the Eastern Tianshan: Implications for the evolution of the southern Altaids

Permian−Triassic metaluminous−peraluminous granitoids, mafic−ultramafic plutons, and Ni-Cu and Au deposits are prominent features in the Eastern Tianshan of the southern Altaids. However, the genetic relationship between coeval granitoids and mafic−ultramafic intrusions, and the geodynamics of magmatism and related mineralization, remain ambiguous. To address these ambiguities, we present petrological, geochemical, and bulk-rock Sr-Nd-Fe and zircon U-Pb-Hf isotope analyses of granitoids from the Shuangchagou Complex and gabbros from the Huangshandong Complex in the Eastern Tianshan. Zircon U-Pb ages demonstrate that the Huangshandong gabbro was emplaced at ca. 277.8 ± 1.4 Ma. In contrast, U-Pb ages determined from zircons in the granitic rocks of the Shuangchagou Complex suggest that the complex crystallized from three stages of magmatism: (1) strongly peraluminous S-type granitic magma represented by early-stage gneiss and granitic veins (ca. 289 Ma), (2) metaluminous to weakly peraluminous I-type granitic magmas represented by the intermediate-stage granitoids (ca. 283−261 Ma), and (3) late-stage granitoids (ca. 250−241 Ma). The intermediate- and late-stage granitoids (ca. 283−241 Ma) show clear enrichments in the light rare earth elements and large ion lithophile elements (e.g., Rb, Th, and U), and depletions in high field strength elements (e.g., Nb, Ta, and Ti), similar to arc magmas, which indicates that the North Tianshan oceanic plate was still subducting during the Middle Triassic. Considering the diversity of magmatic rocks (e.g., mid-oceanic-ridge−type mafic rocks, and I-, S- and A-type igneous rocks), mineralization styles (e.g., Alaskan-type Ni-Cu sulfide deposits and orogenic gold deposits), and the dextral strike-slip faults (e.g., Kanggur Fault) that occurred concurrently in the Eastern Tianshan during the Early Permian to Middle Triassic, we suggest that splitting of the subducted portion of the North Tianshan oceanic plate created a slab window that allowed the upwelling and partial melting of asthenospheric mantle to form the mafic−ultramafic intrusions and related Ni-Cu sulfide deposits. Sustained migration of magma provided the heat necessary to induce partial melting, devolatilization, and desulfurization of crustal materials, producing the Permian−Triassic, high-K to calc-alkaline I- and S-type granitoids, and associated orogenic gold deposits. By integrating the results of this study with published work regarding the Kanggur Accretionary Complex, we suggest that the subduction of the North Tianshan Ocean may have lasted until the Late Triassic.

The Bougrine Zn-Pb deposit, the largest salt diapir-related Mississippi Valley-type deposit in the Eastern Maghreb salt diapir province, Tunisia

The Bougrine Zn-Pb sulfide deposit (5.5 Mt @ 12 % Zn + 2.5 % Pb) in the Eastern Maghreb salt diapir province of Tunisia is located at the northeastern end of the Lorbeus-Bougrine diapir. The several-km large diapir is composed of Triassic evaporite that intruded about 10 km-thick Jurassic and Cretaceous marine sedimentary rocks during the Cretaceous and Tertiary. Mineralization occurs in breccia zones at the contact with the Triassic diapir and in the peridiapiric Cretaceous strata. Most of the ore is stratabound (F2 orebody) with microsphalerite disseminations in organic-rich laminated black limestone of the Cenomanian-Turonian Bahloul Formation, where sphalerite occurs as infill of Globigerina shells, as massive replacement of Globigerina-rich layers, as banded colloform sphalerite and in voids as euhedral, coarse-grained crystals together with skeletal galena and minor marcasite. Abundant degraded oil seepages in the orebodies and their host rocks testify to the existence of a (former) hydrocarbon reservoir.The various sphalerite generations have highly variable Mn and Fe contents; Cd has an average content of 445 ppm; As and Hg contents are in the 200 ppm range; Tl content is about 40 ppm; Ga content is about 10 ppm; and In content is consistently <1 ppm. Fluid inclusions in celestite, coarse-grained late-stage sphalerite and calcite indicate moderate fluid salinities (16 ± 2 wt% NaCl eq.) and moderate temperatures (85 to 146 °C). The empirical trace-element sphalerite geothermometer gives 184 ± 38 °C for the main-stage microsphalerite and the banded colloform sphalerite which have no measurable fluid inclusions.A wide range of δ13C (-13.6 to 5.6 ‰) and δ18O (-19.8 to 33 ‰) values is observed in ore-stage and post-ore calcite. Ore-stage calcite commonly has negative δ13C values reflecting involvement of carbon from organic matter; its δ18O composition with an average of 22.6 ± 2 ‰ (19.7 to 26.0 ‰) may be explained by a moderate-temperature hydrothermal fluid. There is no systematic δ34S variation between and across the different styles of mineralization. The range of δ34S of 6–19 ‰ with a mean of 13 ‰ is close to the δ34S value of local and regional Triassic marine sulfate (δ34S = 16 ‰). Thermochemical reduction of Triassic sulfate, likely mediated by hydrocarbons, is the most probable source for sulfur in the ores. Lead isotope data on galena are within a narrow field of upper crustal signature (206Pb/204Pb = 18.71–18.77; 207Pb/204Pb = 15.66–15.70; 208Pb/206Pb = 38.81–38.97) indicating a homogeneous ore fluid.The major characteristics of the Bougrine ore deposit are typical of Mississippi Valley type Pb-Zn deposits and indicate large-scale fluid circulation likely related to stacking and uplift in the northern Tunisian Nappes Zone during the Miocene. Both the hydraulic load of meteoric water and over-pressured basinal and basement fluids during compressional movements favored southward fluid migration along basement discontinuities and most permeable strata in the Mesozoic-Cenozoic sedimentary pile. Low-pressure domains around salt diapirs in a rifting environment allowed focused upward fluid flow, and the hydrocarbon reservoir of the Bahloul Formation then provided the geochemical trap for efficient base metal deposition.

Deep epithermal Au mineralization at Tuanjiegou, northeast China

To better understand the physicochemical features of deeply mineralized intervals of low-sulfidation (LS) Au deposits, the Early Cretaceous Tuanjiegou Au deposit in northeastern China was characterized as it comprises alteration and mineralization styles that reflect deeper portions of the mineralizing system. From shallow to deeper portions of the Tuanjiegou deposit, the mineralization is zoned from sulfide-poor quartz bands through hydrothermal breccia to deep pyrite–marcasite-rich veinlets that occur along hydrofractures within a granodiorite porphyry stock. The zoned alteration halo is centred on the ore zones, and comprises an inner phyllic alteration zone (illite + quartz + muscovite) and an outer intermediate argillic alteration zone (illite ± smectite), with propylitic alteration being limited. Given that apatite fission track ages are extremely sensitive to the ambient temperatures of 60–120 °C, the overlap in the closure dates of magmatic apatite (108.1 ± 3.8 Ma) and zircon (108.2 ± 1.2 Ma) from the granodiorite porphyry is indicative of shallow emplacement of the granodiorite porphyry, likely at depths slightly >0.7 km. A similar paleodepth (900 ± 188 m) was estimated from homogenization temperatures (291 ± 14 °C) of boiling fluids. Preservation of the deep portions of the Tuanjiegou ore system may imply that the productive ore intervals of poorly explored LS epithermal deposits globally are underestimated. Given the evidence for a magmatic origin of the ore-forming fluids at Tuanjiegou, we highlighted that ore-forming fluids are released initially from a water-saturated, oxidizing felsic melt under low-pressure (∼4 km) conditions.

Regional structural setting of late-orogenic IOCG mineralization along the northern Nautanen deformation zone, Norrbotten, Sweden

The northern Norrbotten ore province in Sweden is one of the most mineralized areas in Europe. Iron, gold and/or copper deposits occur as iron oxide-apatite-style mineralization (IOA, Kiruna-type) as well as iron oxide-copper–gold (IOCG) style. Regardless of mineralization style, most deposits appear to be spatially controlled by a set of crustal-scale Palaeoproterozoic shear zones which share similar structural characteristics and deformation histories.Reappraisal of regional geological and geophysical data, coupled with structural mapping, suggests crustal-scale shear zones form continuous c. N-S-trending zones extending from the Skellefte district in the south into the northern Norrbotten ore province. One example from Norrbotten is a zone that extends SSW from Karesuando in the north towards Svappavaara. While this structure has traditionally been inferred to continue SW towards Arjeplog (i.e. the Karesuando – Arjeplog Deformation Zone; KADZ), we favour its deflection SSE into the Nautanen-Aitik trend, making it a continuous, IOCG-bearing, crustal-scale deformation zone. Similar shear zone geometries can be observed in analogous zones to the west. Most of these crustal scale structures record at least two time-separated deformation events of regional significance. IOA and IOCG deposits form in different tectonic environments, separated in time and overprinting each other.

Deeply Derived Magma Controlling the Polymetallic Mineralization at Shuikoushan, South China: Constraints from Mineral U–Pb Dating and Whole-Rock Geochemistry

Various magmatic–hydrothermal activities have resulted in different styles of polymetallic mineralization in South China. Shuikoushan is a large Fe-Cu-Pb-Zn-Au-Ag orefield situated in fold-and-thrust belts within the South China Block. Two types of granodiorite have been identified in recent drilling work. The early-stage, coarse-grained granodiorite has developed magnetite-bearing skarns in the deep level. The late-stage, fine-grained granodiorite is associated with garnet-hematite–magnetite–pyrite–sphalerite–chalcopyrite-bearing skarns in its contact zone. Away from the garnet-bearing skarn are calcite–quartz–pyrite–sphalerite–galena veinlets in faulted breccia. Fieldwork has identified iron mineralization in both skarns, whereas copper mineralization was only discovered in the garnet-bearing skarns. Lead, zinc, gold, and silver mineralization were observed in the garnet-bearing skarns and faulted breccia. Zircon U–Pb analyses suggested the emplacement of two granodiorite at 167.8 ± 0.8 Ma (MSWD = 1.1, N = 31) and 163.6 ± 0.7 Ma (MSWD = 1.3, N = 32). Apatite and garnet U–Pb dating further indicated the magnetite-bearing skarns of 166.2 ± 1.9 Ma (MSWD = 4.5, N = 27), the hematite–magnetite–sulfide-bearing skarns of 158.6 ± 2.8 Ma (MSWD = 1.3, N = 34), and the calcite–quartz–sulfide veinlets of 159.5 ± 5.2 Ma (MSWD = 1.7, N = 24). The time–space relationship between the two intrusions and hydrothermal activities suggests that the fine-grained granodiorite is responsible for polymetallic mineralization. Whole-rock geochemistry analyses demonstrated the enrichment of LILEs and the depletion of Nb and Ta in two granodiorites, with a slight enrichment in LREEs and flat HREE patterns. These granodiorite bodies therefore belong to high-K calc-alkaline magma generated via the crust’s partial melting. The fine-grained granodiorite generally has a lower HREE and higher Dy/Yb, Sr/Y ratios than coarse-grained granodiorite, corresponding to the source of magma in garnet stable lower crust. The residual garnet keeps ferric iron in melts, leaving the fine-granodiorite more oxidized for copper and gold concentration. Through these analyses and our drilling work, a continuous skarn–hydrothermal–epithermal system has been identified for Cu-Pb-Zn-Au-Ag targeting in Shuikoushan.

Geology, fluid inclusions and C−O−S−Pb isotopic compositions of the Chahmileh Pb-Zn deposit, Central Iran: Implications for ore genesis

AbstractThe Chahmileh Pb–Zn deposit, located northwest of the Central Iran Zone, is a sediment-hosted Pb–Zn deposit in the ‘Yazd-Anarak Metallogenic Belt’. It is hosted in Middle Triassic carbonate rocks and is mainly controlled by NW-trending faults. The main ore minerals are galena and sphalerite with minor chalcopyrite, pyrite, and quartz, dolomite, along with minor calcite and baryte as gangue minerals. Cerussite, hemimorphite, wulfenite, mimetite, smithsonite, malachite and iron oxy-hydroxides are the main non-sulphide ore minerals. The main styles of mineralization are vein-veinlet, breccia, disseminated and replacement in association with silicification and dolomitization. Microthermometry of fluid inclusions in dolomite and quartz indicates that the ore precipitated from a warm to hot basin-derived saline fluid. Dolomite samples have δ13CVPDB and δ18OVSMOW values of −0.99 to +1.99‰ and +20.74 to +25.48‰, respectively, and are plotted in the marine carbonate rocks field. These isotopic values suggest that CO2 in the hydrothermal fluids mainly originated from marine carbonate rock. The δ34S values range from +6.3 to +8.2‰ for galena, +5.9 to +6.2‰ for sphalerite, +1.4 to +3.4‰ for chalcopyrite and +15.0 to +17.4‰ for bayite are compatible with a predominant thermochemical sulphate reduction process, and with sulphur sourced from Triassic seawater. Galena samples have a homogeneous Pb isotopic composition that is indicative of a continental crustal reservoir as the main source of lead and probably for the other ore metals. Based on geology, mineralogy, texture and fluid characteristics, the Chahmileh deposit is classified as a carbonate-hosted Mississippi Valley-type deposit.

LA-ICP-MS U-Pb cassiterite age data of the Sadisdorf deposit link Sn-Li-(W-Cu) mineralization in the eastern Erzgebirge to the collapse of the Altenberg-Teplice Caldera

The Sadisdorf Sn-Li-(W-Cu) prospect in the eastern Erzgebirge (Germany) comprises two distinct styles of magmatic-hydrothermal mineralization, namely greisen-type mineralization at the Kupfergrube site, and stockwork-type mineralization at both the Kupfergrube and the Zinnklüfte sites. Previously, these two sites were regarded as expressions of two temporally distinct mineralization events. In this study, this temporal relation was tested by LA-ICP-MS U-Pb data obtained for 16 cassiterite samples, including samples from both sites and styles of mineralization. All 16 samples define a narrow range of ages between 315.1 ± 1.7 / 3.3 Ma and 311.0 ± 3.1 / 4.0 Ma. All ages overlap within uncertainty, suggesting that mineralization across the Sadisdorf prospect is likely related to the same magmatic-hydrothermal event.On the regional scale, the cassiterite ages suggest that Sn-Li mineralization is associated with late-stage felsic magmatism directly following the collapse (∼314–313 Ma) of the Altenberg-Teplice Caldera. The cassiterite ages also overlap with garnet U-Pb LA-ICP-MS ages of Sn-rich skarn occurrences in the western Erzgebirge (e.g., Breitenbrunn, Antonsthal and Hämmerlein). This observation provides direct evidence that greisen and skarn-hosted Sn mineralization are related to the same period of magmatism. The data indicate that the majority of Sn-mineralization in the Erzgebirge formed after 318 Ma (likely between 318 and 310 Ma), challenging previous models which invoked an older suite of granites (326–318 Ma) as causative source intrusions.

Genetic relationship between skarn and porphyry mineralization at the Saibo copper deposit, West Tianshan, NW China: Constraints from fluid inclusions, H–O–C–S–Pb isotopes, and geochronology

The Saibo skarn–porphyry deposit, located in West Tianshan, NW China, is a large copper deposit discovered recently; however, information regarding the differences and connections between skarn and porphyry mineralization remains limited. Thus, this study aimed to investigate fluid inclusions (FIs), H–O–C–S–Pb isotopes, and U–Pb, and Re–Os geochronology to unravel the origin and evolution of the entire hydrothermal system. Skarn mineralization occurs as stratiform and lenticular in the contact zone between the granodiorite porphyry and Kusongmuqieke Group limestone. We identified four mineralization stages: prograde skarn stage (IS), retrograde skarn stage (IIS), quartz–pyrrhotite–chalcopyrite stage (IIIS), and calcite–quartz–pyrite stage (IVS), and four types of FIs: CH4-rich (C-type), halite-bearing (S-type), vapor-rich (V-type), and liquid-rich (L-type) FIs. The homogenization temperatures (Th) of FIs from stages IS, IIIS, and IVS were 366–419, 271–315, and 174–235 °C, respectively, with salinities of 1.7–46.0, 2.2–9.6, and 4.5–7.7 wt% NaCl eqv., respectively. Porphyry mineralization occurs as veinlet-disseminated ores in the granodiorite porphyry. We identified three mineralization stages: quartz–molybdenite–pyrite stage (IP), quartz–chalcopyrite–pyrite stage (IIP), and calcite–quartz–galena stage (IIIP). Unlike skarn mineralization, only the S-, V-, and L-type FIs were identified, with Th of 332–379, 263–315, and 169–233 °C from stages IP, IIP, and IIIP, respectively, and salinities of 1.9–42.3, 2.2–9.6, and 4.2–6.9 wt% NaCl eqv., respectively. The H–O isotope data indicate that the ore-forming fluids were initially derived from magmatic water and gradually diluted by meteoric water during fluid migration. According to C isotope data and the presence of C-type FIs, fluids from skarn mineralization contained more organic carbon than those from porphyry mineralization. The S–Pb isotope data of sulfides suggest that ore-forming materials are derived from both granodiorite porphyry and the Kusongmuqieke Group, although the latter contributed more to skarn mineralization. Pyrites from porphyry mineralization yielded a Re–Os isochron age of 376.0 ± 7.9 Ma, which was slightly younger than the chalcopyrite Re–Os ages of skarn mineralization (>379 Ma). The granodiorite porphyry, which is considered the ore-causative intrusion, yielded a U–Pb age of 380.8 ± 1.8 Ma. Our results indicate that two styles of mineralization were formed successively at different spatial locations during the emplacement of the granodiorite porphyry in a southward subduction setting of the North Tianshan Ocean. The proposed metallogenic model provides a better understanding of the Saibo skarn–porphyry metallogenic system and is expected to assist in the exploration of similar deposits in the West Tianshan orogenic belt.

The gold mineral systems of the West Qinling orogen, central China: New insight from the Baguamiao gold deposit

The Baguamiao gold deposit is the first large deposit discovered in the West Qinling orogen in central China in the 1990 s. However, the occurrence of invisible gold in the deposit has not been reported. There is also no consensus on whether magmatic activity is involved in the gold mineralization, the style of mineralization, and the mechanism of gold precipitation. In this study, the in-situ trace elements, and chemical mapping of pyrite and pyrrhotite in the Baguamiao gold deposit were carried out for the first time. These data combined with the C-H-O isotope data of quartz, ankerite and calcite were used to determine mineralization process. In the Baguamiao gold deposit, five types of pyrite (Py0 to Py4) and pyrrhotite (Po0 to Po4) were identified, corresponding to the sedimentary-diagenetic period and four stages of mineralization (Stage I to Stage IV), respectively. From stage I to stage IV, gold mineralization in pyrite and pyrrhotite occurs as either visible or invisible crystals. The latter occurs dominantly as lattice-bound solid solutions (Au+) and is related to the content of Cu and Te. Co and Ni contents and Co/Ni ratios indicate that pyrite and pyrrhotite are magmatic-hydrothermal origin and affected by fluid-rock interaction. The change of Se and Te concentrations in pyrite and pyrrhotite indicates that oxygen fugacity (ƒO2) was increased from stage I to stage II, and then decreased during stage III and stage IV. In addition, the δ18O values of quartz, calculated δ18OH2O values of the ore-forming fluids and δ13C values range from 16.9 to 20.3 ‰, 7.7 to 12.9 ‰, and − 19.3 to + 0.2 ‰, respectively. Such isotopic signature records typical characteristics of orogenic gold deposit. The ore-forming fluid is a mixed hydrothermal solution involving metamorphic water, magmatic water, and meteoric water, and mixed with marine carbonate and sedimentary organic matter. Gold was precipitated by phase separation, fluid-rock interaction, and fluid mixing. Combined with the tectono-magmatic evolution, metamorphic deformation, and gold mineralization age of the West Qinling orogen, it can be concluded that with the closure of the Mianlue portions of the East Paleo-Tethys Ocean, the Baguamiao gold deposit was formed in the post-collisional extensional environment between the South China Block and the North China Block in the Late Triassic and is an orogenic gold deposit reference to the crustal continuum model.

Multiple stages of Au mobilization in the Changshagou Au deposit, Eastern Tianshan, NW China: Insights from mineral chemistry and fluid inclusions

Gold deposits involving multiple stages of mineralization have received considerable attention, but the relationship between these Au enrichment episodes remains enigmatic. The Changshagou Au deposit in the Chinese Tianshan Orogenic Belt exhibits two contrasting styles of mineralization. Early stockwork disseminated sulfide mineralization is associated with potassic alteration and acid magmatic fluids (log fO2 = -30 to -25, pH = 3 to 6), whereas late auriferous vein mineralization is associated with silicification and weakly alkaline hydrothermal fluids (log fO2 = -35 to -32, pH = 4 to 8). Early mineralization (average Au grade = 1.8 g/t) is dominated by invisible gold in sulfides, whereas late mineralization (average grade = 3.7 g/t) contains abundant native gold (fineness = 799 to 872). Fluids with high Au solubilities (∼104 ppb) from the late-stage mineralization remobilized pre-existing Au and formed As-enriched overgrowth bands on pyrite, with the core of these pyrite containing up to 1800 ppm Au, but little As, and their rim containing up to 4300 ppm As, but little Au. Subsequent fluid boiling accompanied with the escape of CO2 and H2S elevated the pH and redox state of the fluid (log fO2 = -32 to -28, pH >8), which caused a decrease in Au solubilities and precipitation of native gold (average grade = 28.6 g/t). In summary, we suggest the Changshagou Au deposit formed as a result of three key processes — pre-enrichment, re-mobilization, and re-enrichment — all of which are important to the formation of Au deposits characterized by multiple stages of mineralization.

Au-Cu Resources in Some Mines from Antiquity in the South Gabal Um Monqul and Gabal Al Kharaza Prospects, North Eastern Desert, Egypt

Since Antiquity, sustainable resources of gold and copper have been mined at two prominent prospects in the north Eastern Desert of Egypt, namely the south Gabel Um Monqul (SGUM) and Gabal Al Kharaza (GKZ). Mineralization is hosted by Neoproterozoic shield rocks represented by dacite and monzo- to syenogranite at the SGUM prospect whereas they are diorite, granodiorite, and quartz feldspar porphyry at the GKZ prospect. These hosts have been emplaced in an island arc environment from calc-alkaline magmas with a peraluminous to metaluminous signature. They are hydrothermally altered including albitization, sericitization, silicification, epidotization, and chloritization. The Au and Cu mineralizations are confined to shear zones that lately filled with auriferous quartz veins adjacent to mineralized alteration zones. In the GKZ prospect, the old trenches trend mainly in a NW–SE direction whereas it is NE–SW and NW–SE in the SGUM prospect. Evidence of shearing ranges from megascopic conjugate fractures and shear planes in the outcrops to microscopic sheared and crumbled Au-Cu ore assemblages dominated by Fe-Cu sulfides, specularite, and barite. Microscopic investigation suggests that the formation of specularite is due to the shearing of early existing magnetite. The ore textures and paragenetic sequence indicate that pyrite in the alteration zones is oxidized, leading to the liberation of gold up to 3.3 g/t. The formulae of the analyzed electrum lie in the range Au74.5-76.8 Ag22.2-24.5. Integration of the field, geochemistry, and mineral chemistry data, combined with the gold fire assay data prove the presence of sustainable amounts of disseminated Au and Cu, not only in the mineralized quartz veins, but also in the alteration zones. Data materialized in our paper show similarities in the style of mineralization at the SGUM and the GKZ prospects with iron oxide-copper-gold (IOCG) deposits elsewhere in the Arabian-Nubian Shield (ANS) and other world examples.

The geochemistry, origin, and hydrothermal alteration mapping associated with the gold-bearing quartz veins at Hamash district, South Eastern Desert, Egypt

Integrating diverse techniques and datasets, significantly enhances the accurate identification of various mineral deposits. This work aims to determine different types of mineral deposits in the Hamash district (Southern Eastern Desert, Egypt) by combining structural features (derived from ALOS PALSAR DEM), alteration zones (detected using ASTER and Sentinel-2), and ore mineralogy. Multispectral imaging, such as ASTER and Sentinel-2 satellite data, provides a cost-effective and efficient tool for lithological and hydrothermal alteration mapping utilizing selective band ratios (SBR), directed principal component analysis (DPCA), feature-oriented false-color composites (FFCC), and constrained energy minimization (CEM). The deductions drawn from the analysis of ASTER and Sentinel 2 satellite data are solidly corroborated through meticulous investigations of pre-existing lithological maps in the study area, on-site validation via fieldwork, and robust laboratory analysis, attesting to reliable results. Validation of remote sensing results was performed through field observations, petrographic investigations, X-ray diffraction technique (XRD), and SEM–EDX analyses. Based on ore mineralogy derived from XRD and SEM results the quartz-vein-associated ore minerals in the Hamash district include chalcopyrite, pyrite, hematite, goethite, bornite, covellite, and gold. According to the present paragenesis, the mineralization in the study area is classified into three types: sulfide mineralized zone, transitional zone, and supergene zone. Using an ore microscope, our studies identified that the alteration zones include gold-bearing sulfide minerals as well as the minerals goethite and malachite. In gold-bearing quartz samples, the concentrations of Cu, As, Ag, and Sb are positively correlated with Au at the degree of shear deformation. According to data gathered from the fire assay results, Au content varied from 0.027 to 57.20 ppm, along with Cu (10–6484 ppm), Ag (0.5–20.5 ppm), As (5–2046 ppm), Zn (3–1095 ppm), Pb (2–1383 ppm), and Sb (5–23). Our results confirmed that the Hamash region is one of the most important gold-bearing sites, with gold concentrations ranging from 0.027 up to 57.20 ppm. Furthermore, the current contribution highlighted four stages in the paragenetic sequence of the recorded ores, including magmatic, metamorphic, hydrothermal, and supergene by origin, indicating a considered similarity with the known Egyptian gold sites regarding host rocks, mineralization style, alteration assemblage, and several ore mineral conditions.

Constraints on metallogenic temperature and mineralization style from reflection color of sphalerite

The relationship between the color of sphalerite and trace elements has aroused the interest of researchers since a long time, but most of the study is still in the qualitative stage. In this contribution, we made attempt to reveal the relationship between the reflection color and its trace element, in order to discuss the genetic significance of various reflection colors of sphalerite through the quantitative study of reflection color of sphalerite. Based on LA-ICP-MS analysis and microspectrophotometer analysis of sphalerite samples in different types of deposits, the elements with significant correlation with the reflection color index were found and analyzed by factor analysis. Different genetic types of sphalerites have different color index, The average reflection color indices of each type sample are as follows, sphalerite from Mengya’a deposit: λd = 477.3 nm, Pe = 0.046, Rvis = 17.23%; sphalerite from Zhaxikang deposit: λd = 477.2 nm, Pe = 0.043, Rvis = 16.70%; sphalerite from Nanmushu deposit: λd = 476.4 nm, Pe = 0.038, Rvis = 16.55%. The reflection color index of sphalerite is correlated with the content of Mn, Fe, Ga, Ge, Ag, Cd, In, Tl, Pb. The results of factor analysis indicate that sphalerite with high reflectivity is more abundant in Fe, Mn and In, while the sphalerite with low reflectivity is more abundant in Ge, Tl, Pb and Ag. Furthermore, the reflection color index of sphalerite can be used to distinguish the genetic type of deposits. Based on an obvious linear relationship between the reflection color index of sphalerite and its mineralization temperature, we propose a new empirical equation: T(°C) = 61.4*Rvis + 1.1*λd + 6000*Pe-1533 which can be used as a geological thermometer.

Au-Bi-Te(-Cu) Mineralization in the Wawa Gold Corridor (Ontario, Canada): Implications for the Role of Bi-Rich Polymetallic Melts in Orogenic Au Systems

The Wawa Gold Corridor, a series of Archean orogenic Au deposits in the Michipicoten greenstone belt, Canada, comprises two styles of Au mineralization: (1) syn-deformation gold associated with pyrite and arsenopyrite; and (2) late- to post-deformation gold associated with chalcopyrite and Bi-Te(-S) phases. Through petrographic and mineral–chemical analysis, it was determined that gold in the latter assemblages precipitated from Bi-rich polymetallic melts during hydrothermal overprinting of the earlier Au-As-S mineralization; this event was likely driven by the emplacement of Archean lamprophyres. The formation and evolution of these melts was governed by fluid–pyrite reaction interfaces, where the bulk composition of the melts was broadly controlled by the trace-element chemistry of the sulphide minerals in the local host rocks. This suggests that the melt-formation event involved mobilization of existing metal endowments related to early Au events, rather than addition of new Au, Bi, and Te. Thus, the deposition of high-grade Au by Bi-rich melts was dependent on pre-existing sulphide mineralization, both as a source of metals and as micro-environments that stabilized the melts. The paragenesis documented in the Wawa Gold Corridor (i.e., early hydrothermal Au-As-S mineralization and late melt-related Au-Bi-Te mineralization) has been previously recognized in numerous other orogenic and non-orogenic Au deposits. Herein, it is suggested that this apparent consistency in the timing of melt events across multiple systems probably reflects the physicochemical conditions (i.e., fO2-aH2S) of orogenic fluids being incompatible with molten Bi. Bi-rich polymetallic melts are hence unlikely to form primary Au mineralization in orogenic systems but can, however, have a significant impact on the ultimate deposit-scale distribution of Au via secondary mobilization and enrichment.

Mineralogy and chemistry of columbite-tantalite from Bugarura-Kuluti area, Karagwe-Ankole Belt, Rwanda: Indicators of pegmatite and granite evolution

Our study characterizes in detail the mineralogical, textural, and compositional features of Ta-Nb oxides from the Bugarura – Kuluti deposit located in the eastern Rwanda. The research presents the chemical evolution of oxides at all scales, from a single crystal, through a single host body, to the regional granite – pegmatite scale. Finally, we propose an evolutionary model of a B-rich magmatic – hydrothermal system hosting Ta-Nb-Sn mineralisation. Ta-Nb oxides are hosted by LCT (lithium-caesium-tantalum) pegmatites, rarely in greisens and two-mica peraluminous granites. They display a wide range of composition including all types of columbite group minerals, wodginite, tapiolite and microlite. The internal texture of columbite-tantalite exhibits a multiple zoning pattern indicating primary composition modified by the extreme fractionated, volatile and water saturated residual melt. Hydrothermal origin of columbite-tantalite is observed in greisens, expressed by a higher W concentration and coeval or even younger crystallization compared to the associated cassiterite. Fractionation trend in a crystal scale includes an extreme increase in Ta/(Ta + Nb) ratio with little or no change in Mn/(Mn + Fe), mainly caused by the high Ta solubility in the silicate melt during fractionation. On a regional scale, the pegmatites follow Fe-Mn fractionation trend towards high Mn/(Mn + Fe) compositions. This is due to fractional crystallization of CGM and crystallization of other Fe competing minerals shifting the melt composition towards Mn enrichment. In the outermost pegmatites, the final crystallization stage is characterized by a rapid increase in Fe. Fe enrichment in the residual melt was due to infiltration of meteoric/metamorphic fluids. Tapiolite and wodginite crystallised from the B and H2O undersaturated, Na-rich residual melt carrying Ta mixed with Sn- and Fe-rich hydrous fluids. The difference in fractionation patterns and styles of mineralization between different deposits within Kibara metallogenic province provides the evidence of the complexity of magmatic-hydrothermal systems which developed by partial melting of heterogenous crustal material.

The genetic association between vein and skarn type tungsten mineralization in the Yaogangxian tungsten deposit, South China: Constraints from LA-ICP-MS analysis of individual fluid inclusion

The large-scale Yaogangxian W deposit, located in central of the Nanling metallogenic belt, South China, comprises independent quartz vein-type and skarn-type W mineralization. Wolframite-bearing quartz veins occur invariably in metasandstone and slate to the northwest of the Yaogangxian granitic intrusion, whereas scheelite-skarn are mainly hosted by the limestone to the east. The vertical extension of single wolframite-bearing quartz vein can reach up to 1000 m and we focused on the vein samples collected from the deepest level (26 level) which likely recorded early magmatic fluids. For skarn mineralization, two scheelite precipitation stages were recognized, namely scheelite-1 in retrograde stage and scheelite-2 from sulfide-stage. To reveal the fluid sources and characteristics of two mineralizing systems, detailed petrography and microthermometry analyses were carried out on fluid inclusion assemblages (FIA) in scheelite, wolframite and their coexisting quartz. Fluid compositions were obtained from individual fluid inclusion (FI) in ore and gangue minerals via laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS) analysis. These data aid elucidation on the source and nature of fluids in the two distinct W mineralization styles. The chemical compositions of FIs hosted in wolframite and scheelite points to a common magmatic source. The fluid in the scheelite ore section exhibits lower As and B than the wolframite ore section, indicating that boiling may have occurred at early skarn stage. Fluid evolution in the two mineralizing systems suggest that formation of diverse W mineralization styles is mainly controlled by different host lithology and fluid processes. In the wolframite ore section, ore-forming fluid recorded in the deepest level of vein show elevated As, B, K and Rb contents than previously reported ore-forming fluid obtained from the tip of the vein. This likely indicate absence of intensive fluid immiscibility in the deep during wolframite formation, which may rather be accompanied by fluid-rock interaction. In the scheelite ore section, constant injection of meteoric water is revealed. FI hosted in scheelite-1 and 2 exhibit similar compositions, and the lower K content in scheelite-2 fluid is thought to be caused by sericitization in the retrograde stage skarn. The Mo content of scheelite decreased from the retrograde stage to sulfide-stage, indicating a decrease in oxygen fugacity. Based on these conclusion and previous geological and geochronological studies, we propose a metallogenic model of the coupled wolframite-quartz vein and scheelite-skarn mineralization.