Physicochemical Conditions of Differential Mineralization of Au and As in Gold Deposits,Southwest Guizhou Province,China

The conditions under which gold and arsenic are enriched separately during mineralization in gold deposits in southwestern Guizhou Province were described and the thermodynamic calculations gave: 200–150°C at 400 × 10⁻⁶ -300 × 10⁶ Pa (corresponding to a depth between 1.6 km and 1.2 km); lgf o₂,−40 to -35 Pa; lgf s₂, -20 to−16 Pa; pH 5.0 -4.2 and Eh -0.53 V. This project was jointly supported by the National Natural Science Foundation of China and the Open Lab. of Ore Deposit Geochemistry, Institute of Geochemistry, Chinese Academy of Sciences.     

Petrogenesis and metallogenic setting of porphyries of the Duobuza porphyry Cu–Au deposit,central Tibet,China

Given that the Duobuza deposit was the first porphyry Cu–Au deposit discovered in central Tibet, the mineralization and mineralized porphyry in this area have been the focus of intensive research, yet the overall porphyry sequence associated with the deposit remains poorly understood. New geological mapping, logging, and sampling of an early granodiorite porphyry, an inter-mineralization porphyry, and a late-mineralization diorite porphyry were complemented by LA–ICP–MS zircon dating, whole-rock geochemical and Sr–Nd isotopic analyses, and in situ Hf isotopic analyses for both inter- and late-mineralization porphyry intrusions. All of the porphyry intrusions are high-K and calc-alkaline, and were emplaced at ca. 120 Ma. The geochemistry of these intrusions is indicative of arc magmatism, as all three porphyry phases are enriched in light rare earth elements and large ion lithophile elements, and depleted in heavy rare earth elements and high field strength elements. These similar characteristics of the intrusions, when combined with the relatively high (⁸⁷Sr/⁸⁶Sr)_i, negative ε_Nd(t), and positive ε_Hf(t) values, suggest that the magmas that formed the porphyries were derived from a common source region and shared a single magma chamber. The magmas were generated by the mixing of upwelling metasomatized mantle-wedge-derived mafic magmas and magmas generated by partial melting of amphibolite within the lower crust.The inter-mineralization porphyry has the lowest ε_Nd(t) and highest (⁸⁷Sr/⁸⁶Sr)_i values, suggesting that a large amount of lower-crust-derived material was incorporated into the melt and that metals such as Cu and Au from the enriched lower crust were scavenged by the parental magma. The relative mafic late-mineralization diorite porphyry phase was formed by the residual magma in the magma chamber mixing with upwelling mafic melt derived from metasomatized mantle. The magmatic–hydrothermal evolution of the magma in the chamber released ore-forming fluid that was transported mainly by the inter-mineralization porphyry phase during the mineralization stage, which ultimately formed the Duobuza porphyry Cu–Au deposit.These porphyritic intrusions of the Duobuza deposit have high Mg^# and low (La/Yb)_N values, and show some high LILE/HFSE ratios, indicating the magma source was enriched by interaction with slab-derived fluids. Combined with age constraints on the regional tectonic evolution, these dating and geochemical results suggest that the Duobuza porphyry Cu–Au deposit formed in a subduction setting during the final stages of the northward subduction of the Neo-Tethyan Ocean.     

Heavy metal contamination of soils and waters in and around the Imcheon Au–Ag mine,Korea

The heavy metal contamination of soils and waters by metalliferous mining activities in an area of Korea was studied. In the study area of the Imcheon Au–Ag mine, soils and waters were sampled and analyzed using AAS for Cd, Cu, Pb and Zn. Analysis of HCO₃⁻, F⁻, NO₃⁻ and SO₄²⁻ in water samples was also undertaken by ion chromatography. Elevated concentrations of the metals were found in tailings. The maximum contents in the tailings were 9.4, 229, 6160 and 1640 mg/kg extracted by aqua regia and 1.35, 26.4, 70.3 and 410 mg/kg extracted by 0.1 N HCl solution for Cd, Cu, Pb and Zn, respectively. These metals are continuously dispersed downstream and downslope from the tailings by clastic movement through wind and water. Because of the existence of sulfides in the tailings, a water sample taken on the tailings site was very acidic with a pH of 2.2, with high total dissolved solids (TDS) of 1845 mg/l and electric conductivity (EC) of 3820 μS/cm. This sample also contained up to 0.27, 1.90, 2.80, 53.4, 4,700 mg/l of Cd, Cu, Pb, Zn and SO₄²⁻, respectively. TDS, EC and concentrations of metals in waters decreased with distance from the tailings. The total amount of pulverized limestone needed for neutralizing the acid tailings was estimated to be 46 metric tons, assuming its volume of 45,000 m³ and its bulk density of 1855 kg/m³.     

Triassic Epithermal Au and Porphyry Related Cu-Mo Mineralization of the Chatree Deposit, Central Thailand

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Geological and Geochemical Constraints on the Trinity Pattern of Au Deposits in Ciemas, West Java, Indonesia

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The Constraints on the Differential Enrichment of Au and As During Hydrothermal Mineralization,Southwest Guizhou,China

The differential enrichment of gold and arsenic observed in As-bearing hydrothermal gold deposits in Southwest Gizhou is induced by vapor-liquid separation in response to changing physico-chemical conditions during the hydrothermal evolution and is a reflection of the geochemical behavior of the two elements.     

Intermetallic compounds,copper and palladium alloys in Au–Pd ore of the Skaergaard pluton,Greenland

Copper–palladium intermetallic compounds and alloys (2314 grains) from the Au–Pd ore of the Skaergaard layered gabbroic pluton have been studied. Skaergaardite PdCu, nielsenite PdCu₃, (Cu,Pd)_β, (Cu,Pd)_α, (Pd,Cu,Au,Pt) alloys, and native palladium have been identified as a result of 1680 microprobe analyses. The average compositions and various chemical varieties of these minerals are characterized, as well as vertical and lateral zoning in distribution of noble metals. The primary Pd–Cu alloys were formed within a wide temperature interval broadly synchronously with cooling and crystallization of host gabbro and in close association with separation of Fe–Cu sulfide liquid. In the course of crystallization of residual gabbroic melt enriched in iron, noble and heavy metals and saturated with the supercritical aqueous fluid, PGE and Au are selectively concentrated in the Fe–Cu sulfide phase as Pd–Cu and Cu–Au alloys.     

Tectono-metallogenic settings of the formation and convergence of disseminated Au–sulfide mineralization

Large Au-sulfide deposits (GSDs) of disseminated ores occur worldwide in metallogenic provinces of various ages (from Precambrian to Pliocene). The studies performed showed that the great genetic diversity of GSD is determined by the similar oregenesis conditions that appear in different tectono-metallogenic settings (TMSs). A GSD is included in a certain TMS by the respective changes in the mineral and geochemical assemblages of ores. However, in the majority of cases, the GSDs of different TMSs are convergent (quasi-identical) in the texture, structure, and mineral composition of ores. All types of the above TMSs are found in Russia, which allows forecasting the discovery of new GSDs in each setting.     

Petrogenesis and Mineralization of the Tongshan Skarn Cu–Au Deposit, Lower Yangtze Metallogenic Belt

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Geology,mineralogy, geochemistry and δ34S of sedimentary rock-hosted Au deposits in Song Hien structure,NE Vietnam

The Song Hien rift basin is considered to be one of the most important regions of gold mineralisation in North East Vietnam. A number of gold deposits in the Song Hien rift basin are hosted in Triassic and Devonian sedimentary formations of the basin. The largest among them are the Bo Va, Tham Riem and Khung Khoang deposits. The Bo Va deposit is hosted in carbonaceous sedimentary rocks of Triassic age, whereas the Tham Riem and Khung Khoang deposits are hosted in carbonaceous sedimentary rocks of Devonian ages. Based on the mineral composition of the ores, the deposits can be divided into to two types: (i) pyrite dominated and (ii) pyrite-arsenopyrite dominated. The Khung Khoang is of the first type and the Bo Va and Tham Riem deposits belong to the second type. The isotopic composition of pyrite and arsenopyrite in the Tham Riem deposit however, is close to that for the ores of the Bo Va deposit. The δ³⁴S value for pyrite ranging from −3.7‰ to −7.4‰ and for arsenopyrite ranging from −3.2‰ to 7.4‰. The δ³⁴S of pyrite in the ore from the Khung Khoang deposit however, has a much heavier isotopic composition of +18.9 to +20.2‰. A narrow range of the variation of sulfur isotopic composition of pyrite and arsenopyrite, the presence of visible gold as inclusions, the presence of chalcopyrite, sphalerite and other inclusions in arsenopyrite and pyrite, the large size of the grains of major ore minerals allow us to assume that the primary gold ores of the Bo Va and Tham Riem deposits underwent metamorphic transformations. The absence of arsenic, antimony, mercury and other characteristic elements in the ores of the Khung Khoang deposit, and substantially heavier isotopic composition of sulfur similar to the sulfur isotopic composition of marine sulfates in the Devonian, allow us to assume another source of the ore components, not connected with the Triassic sedimentary rocks of the Song Hien rift.     

The Geological Characteristics of Xiachahe Au Deposit Zhenyuan, Yunnan

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Structural genesis of the Eunsan and Moisan low-sulphidation epithermal Au–Ag deposits, Seongsan district, Southwest Korea

The Seongsan district in the Jindo–Haenam basin of southwest Korea comprises Precambrian gneissic basement, overlain and intruded by Cretaceous volcanic (98–71 Ma) and plutonic (86–68 Ma) rocks, respectively. Haenam Formation volcanic and volcaniclastic rocks are the dominant rock type exposed in the district and are the main host to high-sulphidation (82–77 Ma) and low-sulphidation (79–73 Ma) epithermal deposits. The Eunsan and Moisan low-sulphidation epithermal deposits have similar vein mineralogy, zoned hydrothermal alteration mineral assemblages, structural framework and interpreted deformation events. These similarities suggest that they formed by district-scale hydrothermal fluid flow at about 77.5 Ma. At this time, ore fluid movement along subvertical WNW-trending faults was particularly focussed in dilatant fault bends, jogs, and at intersections with N-trending splays. At Eunsan, Au–Ag ore shoots coincide with these areas of structural complexity, whereas at Moisan, narrower ore zones correspond with several parallel, poorly connected veins. A secondary control on the location of ore zones is the intersection between mineralised WNW-striking structures and rocks of the Haenam Formation. The higher permeability and porosity of these rocks, in comparison with mudstones and siltstones of the underlying Uhangri Formation, resulted in the more efficient lateral migration of ore fluids away from subvertical faults and into wall rocks. The intersection between subvertical WNW-striking faults and the gently dipping Haenam Formation imparts a low angle SW plunge to both ore bodies. WNW-striking post-mineralisation faults displace ore zones up to 100 m and complicate the along-strike exploration and mining of WNW-trending ore zones. Future exploration strategies in the district involve the systematic testing of WNW-trending mineralised structures along strike from known deposits, with a particular emphasis on identifying structurally complex areas that experienced local dilation during the mineralisation event. Poorly exposed regions have historically been under-explored. However, based on the proposed exploration model for the Eunsan and Moisan deposits, these areas of poor outcrop are now considered important target areas for hidden ore bodies using ground-based geophysical exploration tools, such as seismic surveys.     

Sulfur isotope and fluid inclusion geochemistry of metamorphic Cu–Au vein deposits,central Cobar area,NSW, Australia

Vein-type, structurally controlled Cu–Au mineralisation hosted by turbidites of late Silurian to earliest Devonian age, forms an important resource close to the eastern margin of the Cobar Basin. Here we report 103 new sulfur isotope analyses, together with homogenisation temperatures and salinity data for 545 primary two-phase fluid inclusions for the mineralised zones from the central area of the Cobar mining district. A range in δ³⁴S values from 3.8 to 11.2‰ (average 7.9‰) is present. Sulfur is likely to have been derived from rock sulfur/sulfide in basin and basement rocks, but there may be an additional connate-derived component. Homogenisation temperatures (T_h) for inclusion fluids trapped in quartz and minor calcite veins range from near 150°C to 397°C. Fluid inclusions are characterised by a low CO₂ content and low, but variable salinities (2.1–9.1 wt% NaCl equivalent). Generations of inclusion fluids correspond to six paragenetic stages of vein quartz deposition and recrystallisation at the Chesney mine. Primary fluid inclusions in the first two stages were subjected to re-equilibration resulting from increased confining pressure. Their T_h range (151–317°C) is considered a minimum for the temperature of these fluids. Sulfide and gold deposition at Chesney appears to be related to fluids of moderately high T_h (range 270–397°C) associated with the final paragenetic stage. T_h for the ore-related fluids may be close to the solvus of the H₂O–NaCl–CO₂ system and hence near trapping temperatures. Late-stage entry of a hot, moderately saline ore-forming fluid is implicated as the origin of the Cu–Au mineralisation. However, comparison with geochemical data for the vein-style Zn–Pb–Ag deposits at Cobar demonstrates that differences in metal content for individual zones cannot be attributed to major differences in fluid temperature or salinity. Rather, these differences are probably due to variations in source-rock reservoirs and structural pathways along which the ore-forming fluids moved.     

Geology,mineralogy, and geochemistry of fault-controlled hydrothermal Cu–Au mineralization in the Shanmen Volcanic Basin,SE China

The Yukeng–Banling deposit is a typical fault-controlled hydrothermal Cu–Au deposit in the Shanmen Volcanic Basin (SVB), SE China. Ore bodies commonly occur as lodes, lenses and disconnected pods dipping SW with vertical zonation of ore minerals. Ore-related hydrothermal alteration is well developed on both sides of the veins, dominated by silicification, sericitization, chloritization and argillation with a banded alteration zonation. The mineralization can be divided into three stages (stages I, II and III). Native gold is present as veinlets in fractures of fine-grained pyrite from stage II.Zircon U–Pb and Rb–Sr isochron ages indicate that the Cu–Au mineralization is coeval with the Caomen alkaline granite and Xiaokeng quartz-diorite, both emplaced at ca. 102 Ma. Microthermometric measurements of fluid inclusions in quartz and sphalerite from stage II veins indicate that the Yukeng–Banling deposit is an epithermal deposit. Six ore-related quartz grains have δD_H2O values of − 69 to − 43‰, and δ¹⁸O_H2O values calculated using total homogenization temperatures that range from − 2.0 to 0.7‰. All samples plot in an area between the magmatic field and the meteoric line, suggesting that the ore-forming fluids are derived from a mixed source of magmatic and meteoric waters. δ³⁴S values for eight pyrite separates range from − 2.1 to + 4.1‰ with an average of + 1.7‰, and δ³⁴S values for galena and sphalerite are 2.3‰ and 2.2‰, similar to magmatic sulfur. Four alkaline granite samples have Pb isotopic ratios (²⁰⁶Pb/²⁰⁴Pb)_t = 18.175–18.411, (²⁰⁷Pb/²⁰⁴Pb)_t = 15.652–15.672 and (²⁰⁸Pb/²⁰⁴Pb)_t = 38.343–38.800. Three quartz-diorite samples have ratios (²⁰⁶Pb/²⁰⁴Pb)_t, (²⁰⁷Pb/²⁰⁴Pb)_t and (²⁰⁸Pb/²⁰⁴Pb)_t of 18.277–18.451, 15.654–15.693 and 38.673–38.846, respectively. These age-calculated lead isotopic data for alkaline granite are similar to those for the analyzed sulfides. Co/Ni ratios for stage II pyrites range from 1.42 to 5.10, indicating that the Yukeng–Banling deposit records the past involvement of magmatic hydrothermal fluids. The isotope data, together with geological, mineralogical and geochronological evidence, favor a primary magmatic source for sulfur and metals in the ore fluids. Mixing of the Cu- and Au-rich fluids with meteoric water led to precipitation of the Cu–Au veins along NW-trending faults.The Yukeng–Banling deposit, the contemporaneous Caomen alkaline granite and Xiaokeng quartz-diorite in the SVB formed under an extensional setting, due to high-angle subduction of the paleo-Pacific plate. The extensional setting facilitated the formation of Cu- and Au-rich magmas which was derived from enriched mantle and lower crust.     

Chemical composition of rock-forming minerals in granitoids associated with Au–Bi–Cu,Cu–Mo,and Au–Ag mineralization at the Freegold Mountain,Yukon, Canada: magmatic and hydrothermal fluid chemistry and petrogenetic implications

The chemical compositions of rock-forming minerals have been determined for both altered and least-altered igneous rocks spatially associated with numerous mineralized zones (Nucleus Au–Bi–Cu–As deposit, Revenue Au ± Cu and Stoddart Cu–Mo ± W mineral occurrences, and Laforma Au–Ag deposit) across the Freegold Mountain area, Yukon, Canada. Within the study area, K-feldspar has a narrow compositional range (89.4–91% Or), whereas plagioclase spans a wide range (4.4–70.07% An). In all of the investigated samples, T _Ab = T _An = T _Or, suggesting that magmatic equilibrium between the coexisting plagioclase and K-feldspar was maintained. Igneous amphibole phenocrysts from hypabyssal dikes are typically calcic, whereas the Stoddart Cu–Mo ± W, Laforma Au–Ag, and Goldy Au mineralization are associated with Mg-enriched primary amphibole of edenite composition, and Au–Bi–Cu–As mineralization from Nucleus is related to Al-enriched primary amphibole of ferropargasite composition. Primary biotite phenocrysts across the Freegold Mountain area re-equilibrated with oxidized magma (f(O₂) values between 10–13 and 10–11.5 bars, lying between the Ni/NiO and the magnetite/haematite buffers). However, biotite and amphibole phenocrysts from Stoddart, Goldy, Laforma, and the Highway zones crystallized from a more oxidized magma, as indicated by their elevated X _Mg up to 0.65, relative to biotite and hornblende from Nucleus and Revenue characterized by a lower X _Mg (typically < 0.50). This suggests that various sources and (or) rapid emplacement were involved in magma genesis, as further supported by the considerable variation of pressure (1.8–7.3 kb) of amphibole crystallization and of the total Al content in least-altered biotite (2.6–2.9 afu) within the Freegold Mountain area. Biotite and apatite equilibrated within the T range of 520–780°C, consistent with temperatures of equilibration between ilmenite and magnetite, and their compositions indicate that they formed from an oxidized I-type magma. Magma differentiated by fractional crystallization (indicated by the presence of normally zoned plagioclase with Ca-rich cores and Na-enriched outer rims) and multiple magma mixing (supported by the presence of reversed zoned plagioclase and coexistence of normally and reversely zoned plagioclase). Lower X _Mg biotite associated with the mineralized (Cu–Mo ± W) potassic alteration incorporated more F and Cl relative to least-altered biotite with higher X _Mg. In both Nucleus and Revenue Au–Cu mineralizations, secondary biotite composition varies with respect to the associated alteration mineral assemblages. Although secondary biotite in the skarn re-equilibrated with F-poor fluids, secondary biotite from the pervasive biotitization is related to F- and Cl-enriched fluids, and secondary biotite from the phyllitic zone is related to F-, Cl-, and Mg-depleted fluids, thus consistent with a change in mineralizing fluid composition during mineralization.     

Geology,mineralogy, and geochemistry of magnetite-associated Au mineralization of the ultramafic–basalt greenstone hosted Crusader Complex,Agnew Gold Camp,Eastern Yilgarn Craton,Western Australia; a Late Archean intrusion-related Au deposit?

The Crusader Complex, part of the Agnew gold camp of the Lawlers Anticline of the Yilgarn Craton, Western Australia, is located close to or along the contact between the Lawlers Basalt and Agnew Ultramafics units. Au mineralization within the four orebodies that form the Crusader Complex is dominated by very pure Au, containing less than 1 wt.% Ag, with Au variably associated with scheelite, Bi-tellurides and minor chalcopyrite within a magnetite and titanite gangue assemblage. Hydrothermal alteration associated with this style of mineralization is characterized by increasing concentrations of Mo, Be, Li, Sn and Fe and depletions in Na, Cu, Ba, Pb, Mn, Zn, Si, and K relative to protolith concentrations; these enrichments are more typical in orebodies associated with felsic intrusive-related mineralizing systems rather than the more well-known orogenic Au deposits found elsewhere within the Lawlers Anticline (e.g. at Waroonga) and within the greater Yilgarn Craton.We propose that flexures of the contact between the Lawlers Basalt and Agnew Ultramafic units acted as conduits for Au-bearing felsic intrusive-derived fluids and generated structural traps that enhanced fluid flow. The mineralizing fluids that formed the Crusader deposits were derived from the Lawlers granitoid pluton that intruded into the study area. Enhanced fluid flow promoted interaction between hydrothermal fluids and the reactive mafic–ultramafic rock sequence, augmenting the amount of Au that was precipitated during formation of the orebodies at Crusader. The magnetite-dominated quartz- and sulfide-poor intrusion-related mineralization at Crusader contrasts sharply with other late Archean intrusion-related deposits of the Yilgarn Craton that are usually sulfide- and/or quartz-rich. This may in turn suggest that the Crusader deposit represents a new class of under-explored intrusion-derived deposits, possibly opening new mineral exploration opportunities for the Agnew region, and potentially the wider Eastern Goldfields Superterrane. Enrichments in Mo and Sn and significant depletions in Cu suggest that other parts of the Lawlers batholith may also be prospective for base metal mineralization.Integration of stratigraphic interpretation with the identification of key structural fluid pathways and the presence of felsic intrusive bodies, as presented in this study, enables the delineation of the key elements that underlie mineralization at the Crusader Complex. We propose that these key elements provide vital information for future gold exploration models that can be used within other Archean terranes and within the Eastern Yilgarn Craton in particular.     

Zircon and molybdenite geochronology and geochemistry of the Kalmakyr porphyry Cu–Au deposit,Almalyk district,Uzbekistan: Implications for mineralization processes

Copper, gold and molybdenum mineralization of the Kalmakyr porphyry deposit in Uzbek Tien Shan occurs as stockworks, veinlets and disseminations in the phyllic and K-silicate alteration zones developed predominantly in a middle to late Carboniferous intrusive complex composed of monzonite and granodiorite porphyry. Zircon U–Pb dating yielded an age of 327.2 ± 5.6 Ma for the ore-hosting monzonite and an age of 313.6 ± 2.8 Ma for the ore-bearing granodiorite porphyry. Re–Os dating of seven molybdenite samples from stockwork and veinlet ores yielded model ages from 313.2 to 306.3 Ma, with two well-constrained isochron ages of 307.6 ± 2.5 Ma (five stockwork ores) and 309.1 ± 2.2 Ma (five stockwork ores and two veinlet ores), respectively. These results indicate that Cu–Au mineralization post-dated the emplacement of the monzonite, started right after the emplacement of the granodiorite porphyry, and lasted for ca. 7 Ma afterward. The geochronological and geochemical data suggest that the Kalmakyr deposit was formed in a late Carboniferous mature magmatic arc setting, probably related to the latest subduction process of the Turkestan Ocean beneath the Middle Tien Shan. The ε_Hf(t) values of zircon grains from the monzonite vary from +11 to +1.7, with an average of +5.1, and those of zircon grains from the granodiorite porphyry range from +5.7 to −1.8, with an average of +2.4. These data indicate that the magma of both monzonite and granodiorite porphyry was derived from partial melting of a thickened lower crust with input of mantle components and variable crustal contamination, and that there was more mantle contribution to the formation of the monzonite than the granodiorite porphyry. The high rhenium concentrations of molybdenite (98–899 ppm) also indicate major mantle contribution of rhenium and by inference ore metals. The relatively high Eu_N/Eu_N¹ values (average 0.68), Ce⁴⁺/Ce³ values (average 890) and Ce/Nd values (average 36.8) for zircon grains from the granodiorite porphyry than those from the monzonite (average Eu_N/Eu_N¹ = 0.33, average Ce⁴⁺/Ce³ = 624, average Ce/Nd = 3.9) suggest that the magma for the syn-mineralization granodiorite porphyry has higher oxygen fugacity than that for the pre-mineralization monzonite. Based on these data, it is proposed that while the monzonite was emplaced, the oxygen fugacity and volatile contents in the magma were relatively low, and ore metals might disperse in the intrusive rock, whereas when the granodiorite porphyry was emplaced, the oxygen fugacity and volatile contents in the magma were increased, favoring copper and gold enrichment in the magmatic fluids. The Kalmakyr deposit formed from a long-lived magmatic-hydrothermal system connected with fertile magmatic sources in relation to the subduction of the Turkestan Ocean beneath the Middle Tien Shan.     

The relation between Cu/Au ratio and formation depth of porphyry-style Cu–Au ± Mo deposits

Constraints on gold and copper ore grades in porphyry-style Cu–Au ± Mo deposits are re-examined, with particular emphasis on published fluid pressure and formation depth as indicated by fluid inclusion data and geological reconstruction. Defining an arbitrary subdivision at a molar Cu/Au ratio of 4.0 × 10⁴, copper–gold deposits have a shallower average depth of formation (2.1 km) compared with the average depth of copper–molybdenum deposits (3.7 km), based on assumed lithostatic fluid pressure from microthermometry. The correlation of Cu/Au ratio with depth is primarily influenced by the variations of total Au grade. Despite local mineralogical controls within some ore deposits, the overall Cu/Au ratio of the deposits does not show a significant correlation with the predominant type of Cu–Fe sulfide, i.e., chalcopyrite or bornite. Primary magma source probably contributes to metal endowment on the province scale and in some individual deposits, but does not explain the broad correlation of metal ratios with the pressure of ore formation. By comparison with published experimental and fluid analytical data, the observed correlation of the Cu/Au ratio with fluid pressure can be explained by dominant transport of Cu and Au in a buoyant S-rich vapor, coexisting with minor brine in two-phase magmatic hydrothermal systems. At relatively shallow depth (approximately <3 km), the solubility of both metals decreases rapidly with decreasing density of the ascending vapor plume, forcing both Cu and Au to be coprecipitated. In contrast, magmatic vapor cooling at deeper levels (approximately >3 km) and greater confining pressure is likely to precipitate copper ± molybdenum only, while sulfur-complexed gold remains dissolved in the relatively dense vapor. Upon cooling, this vapor may ultimately contract to a low-salinity epithermal liquid, which can contribute to the formation of epithermal gold deposits several kilometers above the Au-poor porphyry Cu–(Mo) deposit. These findings and interpretations imply that petrographic inspection of fluid inclusion density may be used as an exploration indicator. Low-pressure brine + vapor systems are favorable for coprecipitation of both metals, leading to Au-rich porphyry–copper–gold deposits. Epithermal gold deposits may be associated with such shallow systems, but are likely to derive their ore-forming components from a deeper source, which may include a deeply hidden porphyry–copper ± molybdenum deposit. Exposed high-pressure brine + vapor systems, or stockwork veins containing a single type of intermediate-density inclusions, are more likely to be prospective for porphyry–copper ± molybdenum deposits.     

Geological Features and Origin of the Hekanzi Alkalic-Type Mo (Au) Deposit,Western Liaoning Province, NE China

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