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We present coupled textural, elemental, and boron isotopic data of tourmaline from the large Zhunuo–Beimulang collision-related porphyry copper deposits (PCDs) located within the western Gangdese, Tibet. Based on morphology and high-resolution mapping, the tourmaline is classified into three paragenetic generations. The first generation of schorlitic Tur-1 occurs in the monzogranite porphyry as disseminations intergrown with porphyritic K-feldspar and plagioclase. It shows decreasing Fe and Ca and increasing Mg and Al contents from core to rim and has relatively homogeneous δ11B values (− 9.9 to − 8.6‰); low Fe3+/(Fe2+ + Fe3+), Cu, F, H2O, and Sr/Y ratios; and high rare earth elements. These features indicate Tur-1 formed in a low fO2 and metal-poor granitic magma during the pre-mineralization stage. The second generation of porphyritic euhedral Tur-2 is hosted in diorite porphyry enclaves and dikes, where it is intergrown with plagioclase and biotite. It forms part of the schorl-dravite solid solution, with high Fe3+/(Fe2+ + Fe3+), Cu, F, H2O, Sr/Y, and δ11B (− 9.7 to − 5.1‰) values. These features indicate it crystallized from a hydrous, oxidized, metal-, and volatile-rich diorite magma. The third generation of Tur-3 is the most volumetrically important and occurs as veinlets and disseminations in the porphyry, or around Tur-1 and Tur-2. It shows radial and oscillatory zoning and is locally intergrown with chalcopyrite and pyrite within the main mineralization assemblage. It has δ11B values (− 10.5 to − 6.0‰) that overlap with Tur-1 and Tur-2 values. Tur-3 also has variable Fe3+/(Fe2+ + Fe3+), Cu, and volatiles (F and H2O), indicating it crystallized from oxidized to relatively reducing metal- and volatile-rich hydrothermal fluids. Overall, the three generations of tourmaline show a narrow range of δ11B values between − 10.5 and − 5.1‰ that are indicative of a single magmatic source. The high Cu, ferric iron, volatiles, and δ11B values in Tur-2 are interpreted to reflect injection of diorite magma into an open crustal magma storage system that led to the formation of an oxidizing and metal-volatile-rich porphyry system. The three stages of tourmaline formation reflect evolution of the magmatic–hydrothermal system from low fO2 conditions towards more oxidizing, volatile-rich conditions and then a return to more reducing conditions that accompanied Cu precipitation. Overall, the injection of oxidized metal-rich magma into a long-lived magma reservoir is a critical driving force for the development of collision-related PCDs. [ABSTRACT FROM AUTHOR]

The evolution of the magmatic-hydrothermal system that formed the Triassic Erdenetiin Ovoo porphyry Cu-Mo deposit, northern Mongolia, is reconstructed through the study of the sequence of stockwork veining and the petrographic characteristics of the veins, as well as the cathodoluminescence and fluid inclusion characteristics of the vein quartz. Early A veins associated with potassic alteration formed at temperatures ≳ 500 °C under lithostatic pressures. The quartz in these veins shows a blue cathodoluminescence emission and is extensively recrystallized. Subhedral to euhedral quartz crystals contained in AB veins precipitated at the ductile to brittle transition at ~ 400–450 °C. The quartz crystals have cores showing a long-lived purple cathodoluminescence color with well-developed growth zoning, whereas the rims of the crystals lack growth banding and have a brownish-red cathodoluminescence emission. Fluid inclusions in the A and AB veins show elevated CO2 concentrations but show no evidence for immiscibility, implying that Erdenetiin Ovoo formed at ≳ 5 km below paleosurface. Quartz in the A and AB veins is crosscut by molybdenite ribbons. The presence of encapsulated molybdenite and sericite grains along growth zones in the quartz rims of the subhedral to euhedral quartz crystals constrains the timing of Mo introduction and suggests an association with the sericite alteration of the host rocks, which affected 50–60% of the deposit. Elevated Cu grades at Erdenetiin Ovoo are linked to the occurrence of C veins, which consist primarily of chalcopyrite and pyrite. These veins surrounded by halos of sericite-chlorite alteration lack quartz as a gangue mineral, suggesting formation at conditions of retrograde quartz solubility at ~ 400 °C and hydrostatic pressures. Late D veins formed at ≲ 375 °C and hydrostatic conditions. The veins consist primarily of pyrite and are associated with texturally destructive sericite alteration of the host rocks. The study demonstrates that hypogene Cu mineralization at Erdenetiin Ovoo was predated and post-dated by sericite alteration, which has important implications to alteration vectoring in porphyry exploration worldwide. [ABSTRACT FROM AUTHOR]

The Kirazlı deposit is located at the center of the Biga Peninsula metallogenic province, in a geological setting characterized by an extensional tectonic environment. A NNW-SSE trending high-sulfidation (HS) orebody with a total reserve of 33.86 Mt @ 0.69 g/t Au and 9.42 g/t Ag lies beneath the Kirazlı Main zone. A porphyry Cu orebody hosted by Eocene intrusive and volcanic rocks has been intersected by drilling within its vicinity. The HS epithermal deposit is hosted by a partly silicified and brecciated Oligocene volcanic and volcaniclastic sequence consisting mainly of basaltic andesite lava flow and lithic/crystal tuff. Lithogeochemistry and zircon U-Pb radiometric ages allow us to distinguish three distinct high-K calc-alkaline magmatic events at ca. 41, 38, and 32 Ma, sourced by metasomatized mantle melts, which have interacted with the crust during their ascent. Porphyry Cu mineralization took place at 36.7 ± 0.4 Ma (muscovite 40Ar/39Ar age) with subsequent re-opening and base metal deposition. Crosscutting quartz-pyrite-molybdenite veins were emplaced at 33.6 ± 0.2 Ma (molybdenite Re-Os age), and followed by the HS epithermal Au-Ag event at ca. 31 Ma, based on a previous study. Our radiometric data indicate that the Kirazlı deposit has recorded a long-lasting Cenozoic magmatic and metallogenic evolution during about 10 Myr. Our study demonstrates that successive, independent, and overprinting, but genetically unrelated, HS epithermal precious metal, hydrothermal Mo, base metal, and porphyry Cu systems have been active at the same location during protracted extensional tectonics of the Biga Peninsula. [ABSTRACT FROM AUTHOR]

Delineation of hydrothermal alteration zoning is important for exploration vectoring toward mineralization centers in porphyry systems, and shortwave infrared (SWIR) spectroscopy is widely used to map hydrothermal minerals distribution for porphyry Cu exploration. However, the SWIR method cannot effectively detect anhydrous alteration minerals (e.g., K-feldspar) in the potassic zone. Magnetite can be formed by potassic alteration and destroyed by phyllic (quartz-sericite-pyrite) alteration. The relative intensity of these two alteration types can be quantified by magnetic susceptibility. Here, we integrate the SWIR and magnetic susceptibility measurements to map hydrothermal alteration zones at the Pulang porphyry Cu-Au deposit in northwestern Yunnan, one of the largest porphyry deposits in the SW China-mainland SE Asia region. White mica, chlorite, and montmorillonite + kaolinite were identified in ~ 60%, ~ 30%, and ~ 15% of the analyzed samples from the Pulang deposit, respectively. Volumetric bulk magnetic susceptibility (Kbulk) values are high in the potassic-altered rocks, but low in phyllic-altered rocks. Using white mica as a proxy for sericite alteration, white mica-chlorite assemblage for chlorite-sericite alteration, chlorite-epidote-actinolite assemblage for propylitic alteration, montmorillonite-kaolinite-dickite assemblage for argillic alteration, and Kbulk (> 0.5 × 10–3 SI) for potassic alteration, we delineate the alteration zoning at Pulang. From the causative porphyry center outward, four alteration zones are delineated (potassic → chlorite-sericite → sericite → argillic). The ore-distal propylitic alteration was developed both in the shallow and deeper levels of the hydrothermal system, resembling typical porphyry-style alteration zoning patterns. Our work shows that high Kbulk value is a useful vector toward Cu mineralization at Pulang, whereas illite crystallinity (SWIR-IC), white mica Al–OH spectral absorption peak, and chlorite Fe-OH spectral absorption peak are less effective. We highlight that magnetic susceptibility measurement is an effective alteration-mapping method when mineralization is developed in the potassic zone (with largely aspectral minerals such as quartz, K-feldspar, and magnetite), while SWIR scalars are more useful when mineralization is developed in the phyllic and/or propylitic zones. [ABSTRACT FROM AUTHOR]

The genetic link between subduction- and collision-related porphyry Cu deposits (PCD) is still not well understood. The Gangdese porphyry Cu belt (GPCB) in southern Tibet hosts two parallel E–W-oriented metallogenic subbelts, including a southern Jurassic subduction-related and a northern Miocene post-collision PCD subbelt. In this study, we combine new and published whole-rock major and trace element data, Cu isotopic compositions and zircon trace element data of Jurassic magmatic rocks from the GPCB. Combined Sr/Y and La/Yb crustal thickness proxies confirm the south to north geometry of the Jurassic arc-back-arc system across the GPCB. The southern Jurassic magmatic arc rocks have systematically higher whole-rock V/Yb ratios, δ65Cu values and zircon Eu/Eu* ratios compared to those of the northern back-arc region. This suggests that Jurassic southern arc magmas had higher oxygen fugacity and H2O concentration than the contemporaneous northern back-arc magmas, which was controlled by a steep subduction geometry of the Neo-Tethyan oceanic slab. Hydrous and oxidized magmas resulted in Cu enrichment during magma evolution and generation of Jurassic PCD in the southern magmatic arc by inhibiting early sulfide saturation at deep crustal levels. In contrast, the northern back-arc magmas were less oxidized and less hydrous, which triggered early sulfide saturation, resulting in segregation of Cu-bearing sulfides in lower crustal cumulates that provided a favorable metal source for later Miocene PCD in the northern subbelt. Our study indicates that the Jurassic subduction geometry controlled the formation and distribution of Jurassic subduction-related and Miocene post-collision-related PCD in the GPCB. [ABSTRACT FROM AUTHOR]

The southern margin of the North China Craton (SNCC) contains 8 giant (> 0.5 Mt Mo resources), 4 large (0.1–0.5 Mt Mo resources) and many small (< 0.1 Mt Mo resources) porphyry Mo deposits. Their magmatism ages are concentrated within 150–131 Ma, but it is unclear what determines the size of porphyry Mo systems. Herein, we synthesize new and existing data for the Mo-bearing intrusions in the SNCC to investigate the optimal conditions for giant deposit formation. These intrusions share similar whole-rock geochemistry characteristics and highly differentiated features, with SiO2 and K2O contents ranging from 68.55 to 79.13 wt.% and 2.63 to 11.18 wt.%, respectively. They share similar lower crustal sources with a variable input of mantle materials. Their εNd(t) and εHf(t) values range from -19.1 to -12.7 and -29.5 to -9.3, respectively, and indicate no relationship with metal fertility. The similar ΔFMQ values calculated from zircon geochemistry also suggest that the porphyry Mo deposit size is unrelated to magma redox conditions. High magmatic water contents and high differentiation features (SiO2 > 73 wt.%) exhibit significant positive correlations with the deposit size. Therefore, we propose that magma with a high water content triggered by intensive fractional crystallization is the fundamental requirement to produce large Mo endowment in the SNCC. This conclusion is consistent with the criteria that pulsed release of mineralizing fluids from a large magma chamber through fractional crystallization play an important role in the formation of giant porphyry Mo deposits in other molybdenum belts in the world. [ABSTRACT FROM AUTHOR]

Porphyry copper ore-forming magmas worldwide are chemically distinguished from ordinary arc granitoids by lower Zr and by higher Sr/Zr ratios at equivalent SiO2 contents. Low ppm Zr in zircon-saturated melts and high whole-rock Sr/Zr in granitoid samples retaining igneous plagioclase are useful discriminants of Cu-fertile intrusive complexes. These and other chemical discriminants of porphyry-copper-forming melts of tonalite-granodiorite-adamellite composition cannot develop during crystallisation-differentiation at upper-crustal pressures. They indicate unusually high dissolved H2O (≥ 9 wt%) in residual melts at depths near the base of the crust. We compare Zr behaviour during mafic-to-felsic magmatic differentiation in orogenically deforming, copper-mineralised arc segments with behaviour during differentiation in non-orogenic, unmineralised arc segments laterally adjacent along the same subduction zones. In orogenically deforming segments, horizontal compressive stress provides resistance to opening of tensile dyke fractures and promotes entrapment of mantle-derived basaltic melts in magma chambers embedded in hot country rock at Moho-vicinity depths, where magmas cool slowly and residual melts tend to last long enough to experience intermittent chamber replenishment by basaltic melts from the deeper mantle. Over several cycles of replenishment and fractional crystallisation, residual melts acquire high concentrations of inherited chemical components that were largely excluded from cumulus minerals—H2O, Cl, CO2, SO3, etc. Accumulating H2O re-orders the high-pressure crystallisation sequence of igneous minerals in successive cycles and leads to early and prolific production of hornblende and early zircon saturation in mafic melts (< 60 wt% SiO2) of later cycles and leads to low Zr contents of zircon-saturated intermediate-composition residual melts. [ABSTRACT FROM AUTHOR]

The Urumieh-Dokhtar magmatic arc (UDMA), Iran, hosts giant to small porphyry Cu ± Au deposits associated with Miocene post-collisional magmatism. Previous studies suggested that the ore-bearing suites are derived from chalcophile element-rich juvenile lower crustal igneous rocks, and that metal contents in the magmas play an important role in the formation of porphyry Cu ± Au deposits in this region. This study investigates the whole-rock major, trace, and platinum group element (PGE) geochemistry, as well as zircon trace element geochemistry, of six porphyry Cu ± Au ore-bearing suites and three barren suites in the central and southeastern UDMA. The aim is to revisit their petrogenesis and understand the factors controlling the formation of post-collisional porphyry Cu ± Au deposits. The high Mg# and Cr and Ni contents of the most mafic variants of ore-bearing and barren rocks suggest that they are primarily derived from the mantle. However, the ore-bearing magmas from the small Dalli Cu–Au porphyry and barren magmas from central to southeastern UDMA experienced substantial crustal assimilation during evolution. The evolved ore-bearing magmas exhibit high La/Yb and Sr/Y ratios, along with concave upward chondrite-normalized REE patterns and high zircon Ce/Nd and Eu/Eu* values, suggesting that they have undergone amphibole dominant differentiation under hydrous and oxidized conditions. In contrast, the barren magmas are characterized by lower whole-rock La/Yb and Sr/Y and zircon Ce/Nd and Eu/Eu* values with flatter REE patterns, implying plagioclase dominant differentiation. The ore-bearing suites, except for the Dalli suite, have systematically higher Pd and Pt contents than barren suites with highly fractionated PGE patterns (high Pd/Ir). The chalcophile element fertility of the ore-bearing suites, as indicated by high Pd/MgO and Pd/Pt ratios, is comparable to that observed in porphyry Cu deposits found elsewhere. This similarity suggests that the Cu contents of the magma likely played acrucial role in the formation of the porphyry Cu deposits in the central and southeastern UDMA. Late sulfide saturation or small amounts of sulfide segregation may have led to the high Cu and moderate Pd contents of the ore-bearing magmas until the late stage of differentiation. In contrast, early sulfide saturation resulted in significant depletion in all PGE and Cu in the barren magma. The fractionated PGE patterns of the ore-bearing magmas could have arisen due to two potential processes. Firstly, they may have resulted from fractional crystallization of Cr-spinel in the early sulfide undersaturated differentiation. Secondly, the patterns might have been inherited from partial melting of metasomatized lithospheric mantle. The systematic geochemical differences between ore-bearing and barren suites suggest that the more hydrous and oxidized nature and higher Cu contents of the ore-bearing magmas substantially increase the porphyry Cu ore potential in the central and southeastern UDMA. [ABSTRACT FROM AUTHOR]

The Kighal porphyry Cu deposit, in the Arasbaran magmatic belt (AMB), is hosted by Late Eocene to Oligocene volcanic rocks and Miocene high–K calc–alkaline subvolcanic intrusions. The Miocene quartz monzonite stocks host porphyry–style Cu mineralization characterized by potassic, phyllic, argillic, and propylitic alteration zones and an advanced argillic lithocap. The Ar–Ar dating of secondary biotite from the potassic alteration and alunite from the lithocap yields precise ages of 20.10 ± 0.18 Ma and 19.15 ± 0.21 Ma, respectively, documenting the evolution of the hydrothermal system over ~ 1 Myr. Hydrothermal rutile occurs in the deposit from the proximal potassic to distal propylitic alteration zones, and their Ti–Fe–Cr–V–W contents can be used as a fertility indicator which suggests a decrease from the proximal zones towards the distal zones. The geochemical fingerprints of the Kighal (and in general the AMB) igneous rocks reflect a post–collisional arc setting. Their distinctly high Th/Yb and Ta/Yb ratios are typical of high–K calc–alkaline intrusions, suggesting that their parental melts were derived from an enriched upper mantle source modified by slab–derived components. Their 87Sr/86Sr(i) (0.70427 to 0.70452) and 143Nd/144Nd(i) (0.512712 to 0.512754) ratios reveal that the magmas experienced moderate crustal assimilation during their magmatic evolution, also supported by increasing Th/La and 87Sr/86Sr(i) and decreasing εNd(i) values with increasing SiO2 content. The 206Pb/204Pb, 207Pb/204Pb, and 208Pb/204Pb ratios of the intrusions (18.67 to 18.84, 15.60 to 15.66, and 38.83 to 39.06, respectively) reveal a crustal origin. Hence, a post–collisional arc setting is proposed for NW Iran, in which mantle–derived mafic melts underwent a MASH process and ascended into shallow magma chambers in the upper crust associated with moderate crustal contamination, which account for the formation of large–scale porphyry Cu mineralization in the AMB. [ABSTRACT FROM AUTHOR]

Oxygen fugacity (fO2) is a critical factor that controls the formation mechanisms of the porphyry Cu deposits. However, the differentiation of the fO2 in post-collisional Au-mineralized and Cu-mineralized porphyry intrusions remains unclear. The post-collisional Jinshajiang–Ailaoshan metallogenic belt hosts several Eocene Cu–Au–Mo porphyry systems including the Yulong Cu, Machangqing Cu, Chang'anchong Cu, and Beiya Au deposits and contains several barren porphyry intrusions, such as the Jianchuan, Putaishan, and Bailiancun granite porphyries. This study compares the zircon chemistry, magmatic fO2, and petrogenesis among the Cu-mineralized, Au-mineralized, and ore-barren porphyries. Our results show that the fO2 of the Cu- and Au-porphyry systems (average ΔFMQ = + 1.59 ± 0.77) is higher than that of the ore-barren (average ΔFMQ = − 0.43 ± 0.91) granite porphyry. Notably, compared to the Au-mineralized porphyries (average ΔFMQ = + 0.99 ± 0.70), the Cu-mineralized porphyries crystallized from more oxidized magma (average ΔFMQ = + 1.89 ± 0.60). All the Cu-mineralized, Au-mineralized, and ore-barren porphyry intrusions originated from partial melting of a thickened lower crust with minor input from the enriched lithospheric mantle-derived melts. The lithosphere of the Au-mineralized and ore-barren porphyry intrusions was influenced mainly by the slab-derived fluids, whereas the lithosphere of the Cu-mineralized porphyry intrusions was metasomatized by slab-derived melts. Therefore, we propose that the parental magmas for the Cu–mineralized porphyry possibly inherited the high oxidation state of the slab-derived melts and then contributed to the high fO2 of the Cu-mineralized granite porphyries. Collectively, the magmatic processes at deep levels played an essential role in determining the fO2 of the granite porphyry, thus controlling the mineralization diversity. [ABSTRACT FROM AUTHOR]

Most porphyry Cu deposits are formed in magmatic arc settings, but some occur in non-arc environments, such as intracontinental settings. The petrogenesis of fertile magmas for porphyry Cu deposits formed in intracontinental settings is still ambiguous. To address this issue, we performed an integrated study of the late Mesozoic porphyry Cu deposits in the South Qinling Orogenic Belt. Zircon U–Pb ages indicate that these late Mesozoic porphyry Cu deposits were formed at 149–142 Ma, in a postcollisional intracontinental setting. εNd(t) (− 4.5 to − 2.7), initial 87Sr/86Sr (0.7046 to 0.7084), and zircon εHf(t) values (− 3.8 to + 2.2) of the late Mesozoic ore-forming and barren rocks suggest that both originate from Meso-Neoproterozoic juvenile lower crust. Whole-rock geochemical and isotopic characteristics indicate that the ore-forming rocks could be formed by the delamination of thickened juvenile lower crust or by the reaction of mantle with normal juvenile lower crust. The barren rocks could be formed by the partial melting of thickened or normal juvenile lower crust. Whole-rock petrochemistry and reversed anorthite contents and Sr isotope data of zoned plagioclase crystals indicate that the mafic magma was recharged into the ore-forming magma chamber. Due to the injection of mafic magma, the ore-forming rocks obtained higher oxygen fugacity, volatiles, water, sulfur, and Cu contents than the barren rocks. According to the regional tectonic evolution, the late Mesozoic porphyry Cu deposits in the South Qinling Orogenic Belt were formed in an extensional environment due to transformation of the tectonic regime. Large-scale lithospheric extension caused asthenospheric mantle upwelling and crust-mantle interaction, providing the crucial metallogenic conditions. Moreover, the injection of mantle-derived mafic magma into the normal magma is a key factor in the formation of the late Mesozoic porphyry Cu deposits in the SQB and similar porphyry systems in an intracontinental setting. [ABSTRACT FROM AUTHOR]

The Wulong gold deposit (> 80 t Au) is located at the northeastern margin of the North China Craton (NCC). Gold in the most economically important quartz veins (Stages 2 and 3) is associated with a varied assemblage of Bi and Te minerals. Stage 2 is characterized by, in a temporal order, native gold-native bismuth-maldonite-hedleyite, bismuthinite-Bi-sulfotellurides, electrum-hessite-Bi-Pb-Ag sulfosalts, Bi-Pb sulfosalts, and Bi-Pb-sulfotellurides. All of these minerals except maldonite, electrum, hessite, and Bi-sulfosalts are present in Stage 3 veins, which also contain jonassonite and unnamed minerals with stoichiometry of Bi8Te3 and Bi5Te3. These complex Bi mineral assemblages resulted from changes in Pb, Ag, Te and Bi concentrations in reduced hydrothermal fluids both locally and temporally, from Stage 2 to 3. Texturally, approximately 85% of the gold grains are associated with almost all Bi minerals in each main-stage mineralization. Quartz-vein ores from Stages 2 and 3 have high Bi concentrations (up to 7332 ppm) and show a positive correlation between Bi and Au, with Bi/Au ratios > 10. These textural and geochemical associations, together with the occurrence of numerous droplet-like blebs and small inclusion trails of native bismuth and Bi-tellurides with native gold, maldonite, or jonassonite, suggest that Bi-rich melts may have formed from the hydrothermal fluids of Stages 2 and 3, and acted as an Au scavenger in a complex Bi-Au-Pb-Ag-Te system. Hence, the intimate association of Bi and Au at Wulong is the result of Au enrichment via the liquid bismuth collector mechanism. Unlike Wulong, however, other deposits in the NCC, such as Yangzhaiyu (Xiaoqinling district), Guilaizhuang (Jiaodong district) and Dongping (Jidong district), are characterized by low Bi concentrations, and are much richer in Te than Bi, so these systems could not generate low-melting point Bi-rich polymetallic melts. The low-sulfur Bi-Au-Pb-Ag-Te association at Wulong is consistent with that observed in reduced intrusion-related gold systems elsewhere and suggests that hydrothermal fluids may have been derived from the co-located Early Cretaceous diorite-granite porphyry dyke swarm. [ABSTRACT FROM AUTHOR]

Magmatic sources of porphyry deposits in postcollisional settings remain controversial. We have used new and published petrological and geochemical data for the Eocene–Oligocene porphyry Cu ± Mo ± Au deposits in the Sanjiang region, SW China, to address this outstanding issue. New data for three deposits (Machangqing, Tongchang, and Beiya) in the Ailaoshan–Red River porphyry Au-Cu-Mo belt (southern part of the Sanjiang region) suggest that ore-forming porphyries were emplaced at ~ 35 Ma, have high (87Sr/86Sr)i (0.7068–0.7071) and negative εNd(t) (− 6.9 to − 5.0), low zircon εHf(t) (− 5.3 to 4.5), and relatively high δ18O (5.9–9.0‰). Magmatic amphibole phenocryst compositions indicate that the parental magmas are all relatively oxidized (ΔFMQ = 1.7 ± 0.6), and H2O-rich (3.8 ± 0.3 wt% H2O). These results are consistent with those estimated from zircon compositions (ΔFMQ = 1.8 ± 0.8) and high whole-rock Sr/Y ratios (75 ± 31), respectively. Based on the new and published data, we suggest that the parental magmas for the Ailaoshan–Red River porphyry Au-Cu-Mo belt were derived from a preserved juvenile arc lower-crust and the underlying metasomatized subcontinental lithospheric mantle (SCLM) attributed to a Neoproterozoic subduction event, whereas the parental magmas for the Yulong porphyry Cu-Mo belt (northern part of the Sanjiang region) originated from the Permian–Triassic juvenile arc lower-crust and metasomatized SCLM. Additionally, parental magmas for these porphyry deposits are all oxidized and H2O-rich, and we attribute such characteristics to inheritance from mixed mantle-crust sources that were modified by previous oceanic slab subduction. [ABSTRACT FROM AUTHOR]

A current mineral exploration focus is the development of tools to identify magmatic districts predisposed to host porphyry copper deposits. In this paper, we train and test four, common, supervised machine learning algorithms: logistic regression, support vector machines, artificial neural networks (ANN) and Random Forest to classify metallogenic 'fertility' in arc magmas based on whole-rock geochemistry. We outline pre-processing steps that can be used to mitigate against the undesirable characteristics of geochemical data (high multicollinearity, sparsity, missing values, class imbalance and compositional data effects) and therefore produce more meaningful results. We evaluate the classification accuracy of each supervised machine learning technique using a tenfold cross-validation technique and by testing the models on deposits unseen during the training process. This yields 81–83% accuracy for all classifiers, and receiver operating characteristic (ROC) curves have mean area under curve (AUC) scores of 87–89% indicating the probability of ranking a 'fertile' rock higher than an 'unfertile' rock. By contrast, bivariate classification schemes show much lower performance, demonstrating the value of classifying geochemical data in high dimension space. Principal component analysis suggests that porphyry-fertile magmas fractionate deep in the arc crust, and that calc-alkaline magmas associated with Cu-rich porphyries evolve deeper in the crust than more alkaline magmas linked with Au-rich porphyries. Feature analysis of the machine learning classifiers suggests that the most important parameters associated with fertile magmas are low Mn, high Al, high Sr, high K and listric REE patterns. These signatures further highlight the association of porphyry Cu deposits with hydrous arc magmas that undergo amphibole fractionation in the deep arc crust. [ABSTRACT FROM AUTHOR]

The 18 × 4 km Davenda-Klyuchevskoe cluster in the Mogocha mineral district of the Siberian craton hosts gold, silver, molybdenum and copper in six types of mineralization. The general sulphide zoning at the Sergeevskoe and Klyuchevskoe deposits, the largest in the cluster, is similar to porphyry systems, but the orebodies form 4.5 × 1 km multiple linear sulphide-rich quartz-veinlet swarms, rather than a bulk mineralized envelope. Five types of mineralization formed at 162 − 150 Ma. They are clearly overprinted by northeast-striking epithermal Au-Ag carbonate-quartz veins. All mineralization is genetically linked to the Peak Klyuchi subvolcanic centre of Late Jurassic to Early Cretaceous age (159 − 132 Ma) which is part of the Amudzhikan intrusive complex, consisting of early complexly shaped ENE-striking granodiorite porphyry stock and dykes, intruded by magmatic to hydrothermal breccia and five generations of WNW-trending dykes of dioritic porphyry, hybrid porphyry, rhyolite, and ultimate lamprophyre. The dykes control or parallel five types of megastockwork orebodies within a dextral extensional strike-slip duplex. However, Au-Ag epithermal veins follow late-mineral northeast faults, dividing the megastockwork into several domains. The Davenda-Klyuchevskoe cluster is part of the Shilka Mo-(Au-Ag-Cu) metallogenic belt, striking within the Siberian craton just 25 km north in parallel to the Mongol-Okhotsk suture. Geochronological and petrological data suggest that the intrusive complex and its mineralization formed in relation to northward-dipping subduction prior to scissor-like suturing in this segment of the Mongol-Okhotsk Ocean in response to the northward push by the North China and Yangtze cratons towards Siberia. [ABSTRACT FROM AUTHOR]

Currently, 60% of the world’s copper production comes from porphyry copper deposits, often significantly enriched by surface weathering. This paper uses new global datasets and previous work to review the critical processes required for porphyry copper formation and supergene enrichment. Porphyry copper formation requires a subducting arc to create a source magma which traverses a thickened crust subject to high exhumation rates during formation, ranging from 100’s to 1,000’s m/m.y. High exhumation rates potentially trigger magma decompression, causing fluid release, opening fluid pathways along faults and lineaments and/or facilitating telescoping, whereby early porphyry-style mineralization is overprinted and enriched by high-sulfidation mineralization at shallower crustal levels. Later supergene enrichment of the deposit requires precipitation rates > 120 mm/yr and exhumation rates ranging from 10’s to 100’s m/m.y. This allows copper sulfide sources to be continually refreshed for weathering but restricts the amount of erosion. Using the Central Andes, one of the world’s most critical porphyry copper provinces, the understanding gained from analyzing these global databases can explain the temporal and spatial pattern of known deposits. These constraints were used to inform mappable target criteria and data required for mineral exploration at a range of different scales, from orogen (> 100,000 km2), to terrane (100,000–1,000 km2) to arc (1,000–100 km2). The results can be used to help illustrate and inform global exploration strategies for supergene-enriched porphyry copper deposits. [ABSTRACT FROM AUTHOR]

The Xiaoxi’nancha porphyry Au-Cu deposit is located in Yanbian, Jilin Province, NE China. Gold-Cu mineralization is mainly associated with chlorite-sericite alteration. The 40Ar/39Ar age of pre-mineralization hydrothermal biotite in potassic alteration defines a relatively well-defined cluster at ~ 111 Ma to 114 Ma with a total fusion age of 112.0 ± 0.3 Ma. In-situ secondary-ion mass spectrometry U-Pb dating of hydrothermal titanite occurring with chalcopyrite yielded an intercept age of 109.0 ± 2.4 Ma. The similarity between the biotite and titanite formation ages suggests a mineralization age of ~ 110 Ma. Chlorite, quartz and apatite coexist in equilibrium and are closely related to mineralization. The Al-in-chlorite geothermometer indicates a formation temperature of 236–351℃ (mean 309℃), and the quartz-apatite pair yielded an average formation temperature of 306℃. The in-situ δ34S compositions of sulfide have restricted and slightly positive values (pyrite 2.3 to 3.9‰, chalcopyrite 1.6 to 3.8‰ and molybdenite 2.3 to 3.7‰). The fluid δ18O values, calculated assuming quartz-fluid equilibrium, vary from 2.4 to 5.5‰ (average = 4.0‰). Therefore, the ore-forming hydrothermal fluids were of moderate-temperature with predominantly magmatic characteristics. Apatite exhibits distinct variations in structure and composition, and slight variations in oxygen isotopic composition. The areas in apatite with dark BSE textures are characterized by lower δ18O values, Cl contents and temperatures and higher F contents, consistent with the result of water–rock interaction rather than mixing with meteoric water. The water–rock interaction and its resulting cooling, can reduce the metal solubility, likely triggering mineralization at Xiaoxi’nancha. [ABSTRACT FROM AUTHOR]

Porphyry Cu-Mo deposits are magmatic-hydrothermal deposits in which sulfide and oxide minerals precipitate from aqueous solutions. However, many questions remain about the composition and evolution of the magmatic-hydrothermal fluids responsible for mineralization. In response to this knowledge gap at the Qulong porphyry Cu-Mo deposit, Tibet, we present a comprehensive major and trace element dataset for biotite (including halogens) from Qulong to elucidate magmatic-hydrothermal fluid compositions and fluid evolution. Based on genesis and occurrence, biotite is divided into primary (igneous), re-equilibrated (igneous modified by hydrothermal fluids), and secondary (hydrothermal) types. All studied biotite grains are Mg-rich, and XMg values (0.59–0.90) increased during fluid evolution, perhaps controlled by high oxygen fugacity (fO2) and sulfur fugacity (fS2) in the magmatic-hydrothermal fluids. The IV(F) and IV(Cl) values and halogen fugacity of biotite indicate that Cl-rich fluids were dominant during early magmatic-hydrothermal evolution, while later fluids were enriched in F. This is consistent with early Cu and late Mo enrichment in the Qulong deposit. We propose a fluid evolution model based on in situ major and trace element data and cross-cutting relationships between the intrusions and the veins. Iron, Ti, Co, Ni, Zn, and Cl contents decreased, while Mg, Si, Al, Sn, Ge, and F contents increased during the evolution of the magmatic-hydrothermal fluid. Importantly, the increase in Fe, Ti, Co, Zn, and Cl and decrease in Mg, Ge, and F contents in hydrothermal biotite as the core of the deposit is approached (extending to ~ 2.5 km depth) may prove to be an important indicator of high-grade mineralized zones. Finally, this study shows that systematic spatial variations in hydrothermal biotite chemistry can potentially be used as a prospecting tool for porphyry deposits worldwide. [ABSTRACT FROM AUTHOR]

The Tiegelongnan porphyry-epithermal deposit (2089 Mt @ 0.53% Cu, 0.08 g/t Au) is host to a large variety of Cu-sulfide minerals, mainly chalcopyrite, bornite, covellite, digenite, enargite, and tennantite. We used LA-ICP-MS to investigate the trace element geochemistry of the Tiegelongnan Cu-sulfides, as well as pyrite, to understand the correlation between sulfides and trace elements, gold in particular, in the porphyry and epithermal systems. Porphyry mineralization consists of stage 1 chalcopyrite-pyrite ± molybdenite, stage 2 chalcopyrite-bornite, and stage 3 covellite. Epithermal sulfides form stage 4 pyrite-alunite, stage 5 digenite-bornite-chalcopyrite, and stage 6 enargite-tennantite ± tetrahedrite. Stage 2 chalcopyrite (S2 Ccp, median = 9.7 ppm Au) is the primary porphyry Au host, and stage 6 tennantite in alunite veins (S6 Tnt-s, median = 98.0 ppm Au) is the major epithermal Au host. These Au-rich sulfides formed under higher oxidation conditions, suggesting that a high oxidation state favors the incorporation of Au in Cu-sulfides. Gold contents in coeval chalcopyrite and bornite are positively correlated to temperature, and Au is enriched in chalcopyrite over bornite at low temperatures (< 350 ℃). Positive correlations between Au and As and Te in covellite and chalcopyrite result from the reaction of As3+ + (Au+/Ag+) + Te2− ↔ 4Cu+ + S2−. Epithermal chalcopyrite and bornite contain more As and Pd than that in porphyry stages, and high contents of As, Sn, Cd, Zn, Sb, Te, Au, and Bi in epithermal enargite and tennantite are likely the result of partitioning of these elements in sulfides at low epithermal temperatures. Epithermal overprinting likely leached Cu from earlier porphyry stage sulfides to precipitate high Cu-grade epithermal mineralization. The Cu-sulfides and related trace elements show a spatial distribution, potentially useful for the exploration of overprinted porphyry-epithermal systems. [ABSTRACT FROM AUTHOR]

Porphyry Cu deposits (PCDs) are major global exploration targets for Cu, Mo, and Au, and mainly formed in accretionary orogens. This study integrates the whole-rock geochemical and Nd isotopic mapping based on ca. 5000 intermediate to felsic magmatic rocks to characterize the crustal structure and metallogeny of PCDs in the Central Asian Orogenic Belt (CAOB), the world's largest Phanerozoic accretionary orogen. The Nd isotopic maps image clearly the extent of cratons, microcontinents, and juvenile crustal blocks, with the PCDs intimately associated with juvenile crust that is consistent with the conclusions drawn by study in other orogens such as Himalayan–Tibetan. More importantly, PCDs are mainly distributed in the juvenile crust's margin adjacent to cratons or microcontinents, indicating that the external magmatic arcs are favorable sites for PCDs. The ore-forming intrusions of Cu-Au deposits are isotopically more depleted than those of Cu-Mo deposits, implying more input of mantle or juvenile crust materials into magmatic sources of Cu-Au deposits. Crustal thickness proxy mapping shows that Cu-Au deposits formed in thinner crust than Cu-Mo deposits, which could be used to target favorable sites for mineral exploration. The crustal thickness proxy and εNd(t) define a negative linear relationship, which quantifies the contributions of juvenile materials to PCDs in response to the changing crustal thickness, from which a newly proposed crustal maturity index was derived to distinguish the Cu-Au and Cu-Mo PCDs. The structure of the crust plays an important role in localizing PCDs; therefore, the integrated mapping of Nd isotopes and crustal thickness proxy could provide mappable exploration targets of PCDs at the orogen scale. [ABSTRACT FROM AUTHOR]

The Zhaiping Ag–Pb–Zn vein deposit in the Coastal Volcanic Belt of southeastern China, which resulted from subduction of the paleo-Pacific oceanic lithosphere beneath the South China Block, is hosted by Early Cretaceous sub-volcanic rocks (rhyolite porphyry) and younger granite porphyry and quartz porphyry. Three generations of veins have been recognized: (i) pre-ore quartz + pyrite, (ii) syn-ore silver + pyrite + pyrrhotite + base metal sulfides + quartz + sericite, and (iii) post-ore quartz + calcite + fluorite veins. Rubidium–Sr dating of syn-ore pyrite yielded an isochron age of 132.2 ± 2.1 Ma (2σ, MSWD = 2.0, n = 4), which is roughly coincidental with the age of the granite porphyry and quartz porphyry (zircon U–Pb age: ca. 133 Ma). The age data, together with Pb, S, H, and O isotopic compositions, indicate a close temporal and possibly genetic relationship between mineralization and porphyry magmatism at Zhaiping. Geochemical and isotope data demonstrate that the Zhaiping sub-volcanic rocks were derived from partial melting of Proterozoic crustal sources and underwent fractionation of feldspars, monazite, and/or allanite. The 87Sr/86Sr ratios of pre-ore (Aph1) and syn-ore (Aph2) stage apatite are in the ranges of 0.71350 to 0.71441 and 0.71260 to 0.71328, respectively, which are distinct from those of the sub-volcanic intrusive rocks (0.7119–0.7125). The Sr isotope signature, together with lower fluid temperatures (< 360 °C) relative to typical magmatic fluid, points at addition of an external fluid. It is suggested that the sub-volcanic intrusion acted as a heat source that drove the dehydration of, and subsequent fluid circulation within, the host rocks. Lower 87Sr/86Sr ratio but higher Sr content of Aph2 relative to Aph1 possibly indicates continuous fluid–rock interaction and progressive decomposition of feldspar in the host rocks, thus supplying large amounts of Sr and probably Pb to the ore fluid. [ABSTRACT FROM AUTHOR]

The origin of hypogene alteration and mineralization features in the Escondida porphyry Cu deposit resulted from intense overprinting related to three main hydrothermal stages. The beginning of each stage is recorded by deposition of bright quartz crystals on vein walls that precipitated from high-temperature fluids. In the deepest zones of the deposit, the earliest stage started with exsolution of intermediate-density fluids, which transported high concentrations of Cu, whereas Mo was not detected. However, in the shallow zones, the early stage began with depressurization and unmixing of intermediate-density fluids, which generated both a hypersaline and vapour-rich fluid phase, producing an important geochemical segregation between both phases. The transitional stage also started with circulation of intermediate-density fluids but never experienced unmixing. These fluids transported the highest Mo concentrations in the deposit; however, Cu displays lower concentrations relative to intermediate-density fluids from the early stage. The beginning of the late stage was also associated with intermediate-density fluids; however, Cu and Mo were below the detection limits in most of the analysed fluids. During the evolution of the three stages, the fluids experienced gradual cooling, which promoted the precipitation of euhedral and zoned quartz crystals that overgrew the early high-luminescence quartz generations. Sometimes, sulfide minerals display euhedral crystal boundaries with zoned quartz, suggesting that mineralization started during these phases. The latest events detected in each main stage are linked to cooler and low-salinity fluids, from which dark quartz and hypogene sulfides precipitated along microfractures and interstitial spaces developed in the earlier quartz generations. [ABSTRACT FROM AUTHOR]

This paper reports microthermometric and noble gas isotope data for fluid inclusion assemblages (FIAs) with evidence of phase separation, i.e. coexisting vapor-rich and halite-saturated inclusions, hosted in the early-formed quartz stockwork veins and post-magmatic quartz eye crystals in two economic porphyry Cu deposits (PCDs; Sar Cheshmeh and Miduk) and two sub-economic prospects (Sar Kuh and Abdar) from the Kerman porphyry copper belt (KPCB), Iran. The multiphase halite-saturated inclusions (i.e., Type I) in all studied PCDs and prospects had the highest homogenization temperature (Th = 525–594 °C) and salinities (63–73 wt% NaClequiv), whereas vapor-rich inclusions (Type II) had lower Th (362–460 °C). Fluid inclusion data show that like economic PCDs, the sub-economic prospects were formed in a fertile hydrothermal system and benefited from a mineralizing fluid, which evolved from a primary hot (mostly > 400 °C), metal-rich and oxidized fluid (as evidenced by the presence of opaque- and hematite-bearing fluid inclusions) of unknown salinity, which underwent a phase separation process to form both brine and vapor phases in the early stage of mineralization. The helium abundance and its isotopic composition document a mantle-derived magmatic source for the primary ore fluid in the formation of the studied PCDs and prospects (3He/4He ratios ranging from 0.46 to 2.8 Ra, corresponding to a mantle He contribution in ore fluids between ~ 7 and 45%). However, subsequent hydrothermal processes, i.e., vapor–brine phase separation, fluid-rock interaction with crustal rocks, and mixing with meteoric pore water containing dissolved atmospheric (e.g., Ne and Xe) and some crustal noble gases (e.g., Ar), changed the initial noble gas composition of the magmatic ore fluid to predominantly atmospheric- and crustal-like compositions. A significant proportion of mantle-derived He (up to 45%) in high-temperature (513–594 °C) and high-salinity (61.5–73 wt% NaClequiv) FIAs may indicate the existence of buried, economic, porphyry Cu mineralization in the Abdar prospect; therefore, it is suggested to be a possible target for further exploration. Comparing the He and Ar noble gas isotope composition in porphyry copper systems of different size and economic importance in this study showed that the ore-forming fluids of the outsized PCD (i.e., Sar Cheshmeh) have higher contributions of crustal-derived fluids characterized by predominantly radiogenic noble gas signatures (4He and 40Ar) than the smaller PCDs. This could have been achieved by a prolonged hydrothermal circulation in a large volume of crustal rocks containing radiogenic noble gases under a long-lived heat regime resulting from a deeply emplaced and slowly cooled composite intrusive body. [ABSTRACT FROM AUTHOR]

Tourmaline is widespread at the Bilihe porphyry gold deposit in Inner Mongolia, China. Five types of tourmaline are recognized based on their occurring locations and microscopic structures: (1) Tur-A in quartz–magnetite ± K-feldspar veins and related potassic-altered rocks, (2) Tur-B in auriferous quartz veinlets, (3) Tur-C in the intermediate argillic shell, (4) Tur-D in late quartz–carbonate–tourmaline–pyrite veins, and (5) Tur-HB in hydrothermal breccia pipes, consisting of three sub-generations (Tur-HB1, -HB2, and -HB3). Almost all these tourmalines have a schorlitic–dravitic composition and belong to the alkali group. Most of the tourmalines contain high Al contents, which may suggest that the fluids are Al-enriched, and that (□Al)(NaFe)-1 and (AlO)(R2+)-1(OH)-1 exchanges have dominated their elemental substitutions. Tur-A and -B yield similar REE patterns with no strong fractionation of LREE and HREE, whereas LREE-enrichment and HREE-depletion characterize Tur-C and Tur-D; Tur-HB1 and -HB2 have flat REE patterns. Tourmalines in hydrothermal veins always show negative Eu anomalies, whereas the ones replacing plagioclase in the altered rocks yield positive Eu anomalies. The mineral precipitation and assimilation of host rocks probably both contributed to the variable compositions of Bilihe tourmaline. Tur-A−D from the main orebody all yield positive δ11B values ranging from +0.7 to +6.3‰, whereas Tur-HB1−HB3 from the hydrothermal breccia pipe show negative δ11B values of −8.8 to −3.5‰. Magmatic hydrothermal fluids enriched in isotopically light boron could have dominated the formation of Tur-HB. In contrast, the heavy boron in Tur-A−D was probably leached from the widespread marine carbonates around the deposit. Systematic contrasts in the trace element compositions of tourmaline from different mineralization types and granitic rocks suggest that (Sn + Li) vs. (Ni + V + Zn), (∑REE + Y + Zr) vs. (Ni + V + Zn) and V vs. Zn are potential elemental groups for distinguishing tourmaline from different environments. [ABSTRACT FROM AUTHOR]

Field mapping, drill-core logging, petrography, laser ICP-MS analysis on pyrite, chlorite geothermometry and geochemical analysis of hydrothermally altered rocks reveal two distinct styles of gold mineralisation at Mt. Percy. The first style is D2 shear zone-hosted and correlates with Fimiston-style mineralisation documented in the Golden Mile. Laser ICP-MS analyses on pyrite indicate high As concentrations (average of 5823 ppm for pyrite in Hannans Lake Serpentinite and 635 ppm in feldspar-quartz porphyry). Chlorite geothermometry reveals average temperatures of 262 ± 50 °C and 357 ± 50 °C in distal and proximal alteration zones, respectively. Geochemical analyses reveal (1) positive gold-silver and gold-antimony relationships; (2) lack of a base metal-gold relationship; (3) systematic increase of carbonatisation and alkali saturation indices from distal to proximal alteration zones; and (4) addition of K, Ca, Na and V, with corresponding depletion of Mg, Fe, P and REE. The second style is related to D4 sheeted quartz vein sets and correlates with Mt. Charlotte-style mineralisation documented in the Mt. Charlotte deposit. Laser ICP-MS analyses on pyrites reveal low As concentrations (average of 51 ppm for pyrites in feldspar-quartz porphyry and 870 ppm in Devon Consols Basalt). Chlorite geothermometry reveals an average temperature of 325 ± 50 °C on vein selvage in the Devon Consols Basalt. High-grade gold mineralisation (> 50 g/t Au) and extensive (< 50 m wide) hydrothermal alteration zones coincide with D2 shear zones and D4 fault-controlled sheeted quartz vein sets, and particularly in areas where both of these structures intersect porphyry stocks. [ABSTRACT FROM AUTHOR]

The Cu-Au deposit of Bor (Serbia) represents a continuum of mineralization styles, from porphyry-style ore occurring in quartz-magnetite-chalcopyrite veins and chalcopyrite disseminations to high-sulfidation epithermal Cu-Au ores in pyrite-chalcopyrite and anhydrite-sulfide veins. Decisive for the great economic importance of Bor is the presence of exceptionally rich high-sulfidation massive sulfide orebodies, composed of pyrite + covellite + chalcocite/digenite and minor anhydrite and enargite. They form irregular bodies measuring 0.5–10 million tons of ore grading up to 7% Cu, hosted by andesites and surrounded by intense argillic alteration. This study focuses on a small but rich underground orebody mined out recently, where limited drillcore is preserved for quantitative geochemical study. This paper documents the vein relationships within the deep porphyry-style orebody of Borska Reka, the transitional porphyry-epithermal veins, and the overlying and laterally surrounding epithermal massive sulfides of the Bor deposit. Geological observations indicate that the formation of massive sulfide orebodies concludes the ore formation. Mass balance calculations, recast into geologically realistic bulk fluid-rock reactions, confirm textural evidence that near-isovolumetric replacement of andesite host rocks is the dominant formation mechanism of massive sulfide orebodies at Bor, whereby all lithophile elements including Si are dissolved and only Ti stays relatively immobile. While net volume changes for individual mineralization styles within the massive sulfide orebody vary from − 16% volume loss to + 127% volume gain, overall volume change for the whole massive sulfide orebody was probably slightly negative. Brecciation is important only as means of creating channelways for reactive fluid that turns the andesite protolith into massive sulfide, whereas net breccia infill occurred only locally. [ABSTRACT FROM AUTHOR]

The reduced nature of the subducting slab has been used to explain the relatively poor endowment of economic porphyry copper deposits in Paleo-Tethyan arc systems. The presence of numerous porphyry Cu deposits in the southern Yidun terrane potentially challenges this model, because these deposits are thought to be the product of Paleo-Tethyan subduction. To investigate this, two representative deposits (i.e., Pulang and Songnuo porphyry Cu deposits) from the southern Yidun terrane have been studied. Zircon U-Pb ages of pre- and syn-mineral porphyries in Pulang are 221 ± 2 Ma (MSWD = 0.89) and 215 ± 2 Ma (MSWD = 1.50), respectively. Zircon and garnet U-Pb ages of the Songnuo syn-mineral porphyry are 217 ± 2 Ma (MSWD = 1.15) and 223 ± 5 Ma (MSWD = 0.97), respectively. The Pulang and Songnuo porphyries both have high whole-rock Sr/Y ratios with minor or no negative Eu anomalies, consistent with derivation from hydrous magmas that underwent minor early plagioclase crystallization but abundant amphibole fractionation. The two porphyry intrusions are characterized by high large-ion-lithophile elements (LILE: Th, U, Ba, Rb) abundances, and low concentrations of high-field-strength elements (HFSE: Nb, Ta, Ti, Zr, Hf). They have similar initial Sr isotope ratios from 0.7055 to 0.7073, ƐNd (t) values from − 4.3 to − 1.6 and zircon ƐHf (t) values of − 1.81 ± 1.34 (n = 47) that are distinct from published results for the Permian–Early Triassic Paleo-Tethyan arc granitoids in the Sanjiang region but similar to the Neoproterozoic arc intrusions in the nearby western Yangtze craton. The Pulang and Songnuo porphyries have relatively high zircon EuN/EuN* ratios (0.59 ± 0.04, n = 52) and calculated Δ log fO2 (FMQ) values (1.61 ± 0.23, n = 52), consistent with relatively oxidized magmas. This feature is similar to the published data for the Neoproterozoic arc intrusions (EuN/EuN* = 0.55 ± 0.08; Δ log fO2 (FMQ) = 2.14 ± 0.60), but distinct from the published data for the reduced normal Paleo-Tethyan arc magmas (EuN/EuN* = 0.29 ± 0.10; Δ log fO2 (FMQ) = − 0.68 ± 0.88). Given that the most recent tectonic reconstruction models suggest that the Paleo-Tethys Ocean closed before ~ 220 Ma, we propose that the Pulang and Songnuo porphyries Cu deposits were formed in a postsubduction setting from oxidized melts generated by reactivating the Neoproterozoic arc root, unrelated to Paleo-Tethyan subduction. [ABSTRACT FROM AUTHOR]

The reduction of oxidized sulfur is essential in porphyry copper deposits whose mineralization predominantly comprises copper sulfides, whereas their source magmas are oxidized with most of their sulfur as SO42− and with exsolved fluids having SO2>>H2S. To estimate the redox state of sulfur, we examined drill cores that intersect potassic and unaltered intrusive rocks in the deeper levels of the Grasberg porphyry copper-gold deposit. Magmatic oxybarometers such as the amphibole-titanite-magnetite-quartz assemblage, anhydrite, and amphibole consistently show that Grasberg ore-forming magmas were oxidized with fO2 > FMQ+3. Initial hydrothermal events formed sulfide-free, anhydrite-rich K-feldspar, and biotite alteration, followed by successive vein stages of (1) magnetite, (2) biotite, (3) quartz, (4) anhydrite-chalcopyrite, (5) chalcopyrite ± sericite selvages, and (6) pyrite-chalcopyrite-quartz + sericite selvages. The δ34S values of sulfide-sulfate mineral pairs indicate SO2-derived SO42− and H2S in SO42−/H2S molar proportions of ~ 4:1 to ~ 3:1 at > 550 °C. The hydrothermal fluid then likely followed a rock-buffered trajectory and became more reduced at < 550 °C. Hydrothermal biotite that replaces igneous amphibole and biotite has a phlogopitic composition, suggesting that Fe2+ was liberated from igneous mafic minerals and oxidized by reaction with SO42− to form magnetite, resulting in sulfide formation by the simplified reaction 12FeO + SO42− + 2H+ → 4Fe3O4 + H2S. [ABSTRACT FROM AUTHOR]

Understanding the magmatic-hydrothermal cooling and exhumation history is fundamental for investigating porphyry deposit formation and preservation. In the Zhunuo porphyry copper deposit of southern Tibet, hydrothermal biotite related to early potassic alteration likely formed from 14.7 ± 0.3 Ma (zircon U-Pb age) to 14.23 ± 0.13 Ma (molybdenite Re-Os age) and cooled below the closure temperature for 40Ar/39Ar system at 13.91 ± 0.05 Ma (hydrothermal biotite 40Ar/39Ar plateau age). The 40Ar/39Ar spectra of another hydrothermal biotite sample that was selectively replaced by chlorite record the timing of late phyllic alteration at 13.53 ± 0.08 Ma. Zhunuo hydrothermal alteration and mineralization likely ceased at 13.09 ± 0.07 Ma based on the 40Ar/39Ar plateau age of the fresh magmatic biotite crystals. The biotite 40Ar/39Ar systematics have not been reset by ~ 12.0 Ma post-mineralization granite porphyry within ore district, which is likely due to rapid cooling and/or absence of fluid exsolution for the granite porphyry. In combination with previous zircon U-Pb and molybdenite Re-Os data, two-pulses of magmatic-hydrothermal activity from 14.78 ± 0.11 to 14.44 ± 0.05 Ma and from 14.23 ± 0.13 to 13.53 ± 0.08 Ma can be recognized at Zhunuo. (U-Th)/He thermochronological data on zircon and apatite from the inter-mineralization monzogranite porphyry suggest three cooling events characterized by first-stage magmatic cooling at a rate of ~ 1850 °C/m.y., and two later phases of uplift and exhumation at ~ 70 °C/m.y. and ~ 10 °C/m.y. Approximately 1.4-km thickness of materials have been removed from the Zhunuo Miocene monzogranite porphyry during uplift and erosion, including a large volume of ore. [ABSTRACT FROM AUTHOR]

The evolution of the magmatic-hydrothermal system that formed the Eocene Yulong Cu-Mo porphyry deposit of the eastern Tibetan Plateau, China, is reconstructed based on the study of the sequence of stockwork vein sets showing systematic crosscutting relationships in hand specimen. Early A veins associated with potassic alteration of the porphyritic host are composed of vitreous quartz that is extensively recrystallized and has a dark blue cathodoluminescence. Fluid inclusions contained in the quartz have been affected by post-entrapment modification. Some of the A veins were reopened and contain ribbons of microscopic molybdenite flakes. Formation of the molybdenite was associated with recrystallization of the earlier formed quartz and concomitant with the development of a dark purple to brownish cathodoluminescence signature. Reopening of the early veins also resulted in the formation of AB veins containing euhedral quartz crystals that contain encapsulated molybdenite flakes and are intergrown with coarse laths of molybdenite. These euhedral quartz crystals showing a dark purple to brownish cathodoluminescence host vapor-rich, intermediate-density fluid inclusions as well as hypersaline liquid and vapor-rich fluid inclusions, indicating that fluid immiscibility at hydrostatic pressure conditions occurred during crystal growth. Later, C veins that crosscut and commonly reopen the earlier A and AB veins lack quartz as a gangue mineral and consist entirely of chalcopyrite and pyrite with minor molybdenite. Sulfide formation was accompanied by chlorite or sericite alteration of the wall rocks. Late D veins containing quartz and pyrite with associated sericitic alteration of the porphyritic wall rocks crosscut all earlier vein types. Only minor amounts of molybdenite and chalcopyrite are present. Euhedral quartz crystals in the D veins contain liquid-rich fluid inclusions that have not been affected by post-entrapment modification. The results of this study indicate that Mo and Cu mineralization at Yulong was introduced by single-phase, intermediate-density magmatic-hydrothermal fluids as the porphyry system was transitioning from ductile to brittle conditions. The bulk of the Mo endowment predated Cu mineralization and formed during the change from lithostatic to hydrostatic conditions and associated immiscibility of the magmatic-hydrothermal fluids. Chalcopyrite precipitation followed as the single-phase, intermediate-density magmatic-hydrothermal fluids was escaping into the hydrostatic-pressured regime. Cooling of the magmatic-hydrothermal fluids appears to have been the principal control on metal precipitation. [ABSTRACT FROM AUTHOR]

Trace element composition of hydrothermal quartz reflects the P-T-X conditions of the mineralizing fluids and can be a potential tracer of the fluid evolution. To explore this potential, quartz trace element data from 21 porphyry Cu-(Au-Mo) and epithermal polymetallic deposits were compiled. In addition, quartz trace element data from six granite-related systems (granite, pegmatite, greisen, Sn-W-Mo veins) and from a subset of calc-alkaline arc-related volcanic rocks were also compiled for comparison. For porphyry Cu-(Au-Mo) deposits, quartz compositions are from publications in which the sequence of quartz-bearing veins and their potential reopening were documented as well as their precipitation temperatures and pressures. The compiled dataset shows that trace element composition of quartz continuously evolved between the different porphyry veins and quartz generations (A, B, C, D, and E). The observed evolution reflects the cooling and/or compositional variations of the hydrothermal fluids. The quartz Al/Ti, Sb/Ti, Ge/Ti, and (Sb+Ge)/Ti ratios allow for the discrimination of quartz from different vein generations of porphyry Cu-(Au-Mo) deposits. This study shows that quartz composition preferentially combined with cathodoluminescence images is an efficient proxy for tracing the evolution of the hydrothermal fluids in porphyry systems and can be used as a vectoring tool to target the centers of porphyry systems. [ABSTRACT FROM AUTHOR]

The Zhunuo porphyry copper deposit in the Gangdese belt of southern Tibet contains 2.37 Mt at 0.57% Cu. In this deposit, Eocene rhyolite (51.6 ± 1.0 Ma) and quartz porphyry (49.1 ± 0.6 Ma) were intruded by monzogranite (14.7 ± 0.3 Ma) and monzogranite porphyry (14.5 ± 0.2 Ma) which commonly host mafic microgranular enclaves (14.9 ± 0.3 Ma). Late-mineralization diorite porphyry (14.2 ± 0.2 Ma) and post-mineralization lamprophyre dikes (12.2 ± 0.1 Ma) and granite porphyry (12.0 ± 0.2 Ma) crosscut the Miocene intrusions. Two quartz–molybdenittie veins yielded molybdenite Re-Os model ages of 14.8 ± 0.1 Ma and 14.4 ± 0.1 Ma, and another two quartz–muscovite–llite–pyrite–molybdenite veins yielded molybdenite Re-Os model ages of 14.2 ± 0.1 Ma and 13.5 ± 0.1 Ma. Zhunuo is characterized by early potassic alteration and associated quartz A veins centered on the monzogranite porphyry and adjacent monzogranite, distal propylitic alteration in the rhyolite, and late-stage phyllic alteration and associated quartz B veins, followed by D veins that affected quartz porphyry and potassic-altered rocks. Copper ores are mainly distributed in the potassic alteration zone that was overprinted by phyllic alteration. Copper mineralization likely occurred during potassic alteration stage and was locally remobilized and redeposited during phyllic alteration stage, or occurred during phyllic alteration stage. The post-mineralization granite porphyry has lower whole-rock Sr/Y (< 20) and εNd(t) (− 9.3 to − 9.0) and higher zircon U/Yb (4 to 27) than the Miocene intrusions (Sr/Y > 40; εNd(t) = − 6.9 to − 6.1; U/Yb = 1 to 10). Limited input of juvenile melts could explain the low potential for copper mineralization in the post-mineralization granite porphyry at Zhunuo. [ABSTRACT FROM AUTHOR]

The giant Jiama polymetallic ore deposit is a porphyry–skarn system in the eastern Gangdese porphyry belt of the Tibetan Plateau. Steeply dipping high-grade massive sulfide veins are classified as lode-type high-sulfidation (HS) mineralization comprising mainly Cu-sulfosalts in Au-poor and Au-rich veins. Au-poor veins contain an As-rich pyrite–enargite–tennantite assemblage, whereas Au-rich veins contain an Sb-rich enargite–luzonite–tetrahedrite–chalcostibite–watanabeite assemblage. The coexistence of pyrite, dendritic muscovite, and euhedral quartz in the Cu-sulfosalts indicates slightly acidic or near-neutral formation conditions. Most Au- and Ag-bearing minerals are inclusions of tellurides (hessite, sylvanite, and petzite) in tennantite–tetrahedrite, and watanabeite. Au and Ag concentrations in tennantite–tetrahedrite, watanabeite, and chalcostibite are much higher than in enargite and luzonite, confirming that they were controlled by intermediate-sulfidation state Cu–As–Sb–S solid solutions, with Au tending to be enriched in Sb-rich minerals compared with As-rich solid solutions. The HS veins overlying the known porphyry intrusion and cutting skarn orebodies in the Jiama deposit constitute a porphyry–skarn–high sulfidation system. The occurrence of HS veins suggests that channels in paleo-fumaroles and the mineralization that resulted may be ascribed to expansion of magmatic vapor. HS veins close to the porphyry intrusion exposed at the surface indicate that shallow epithermal disseminated mineralization was likely removed by rapid regional uplift and erosion of the Gangdese porphyry belt. [ABSTRACT FROM AUTHOR]

The Late Triassic Guichon Creek batholith is a large (~ 1800 km2), composite, zoned batholith that hosts several large porphyry Cu-Mo deposits of the Highland Valley Copper district. The batholith consists of intrusive rocks that range in composition from gabbro to quartz monzonite. Adjacent to the mafic margin of the batholith is the Gump Lake granodiorite to quartz monzonite stock. A new U-Pb zircon age of 218 ± 0.18 for the Gump Lake stock indicates that magmatism in the region began at least seven million years prior to the emplacement of the main Guichon Creek batholith rocks at 211 Ma. Zircons from fifteen samples from the Guichon Creek batholith were analyzed by laser ablation ICP-MS to characterize the magmatic evolution and ore fertility of the batholith. The trace element composition of zircon record early, lower crustal, fractional crystallization followed by five pulses of magma recharge and mixing in an upper-crustal, oxidized, magma chamber as well as degassing of the magmatic-hydrothermal fluids that formed the porphyry copper deposits. Zircons from the early barren rocks have chondrite-normalized Eu/EuN* values of 0.19 to 0.56 and estimated temperatures of 850 to 750 °C. The middle to late intrusions that host porphyry copper mineralization have zircon Eu/EuN* values of 0.30 to 0.74 and slightly lower estimated temperatures of 800 to 600 °C. Late porphyritic stocks and dikes from the mineralized centers contain zircon crystals elevated in Y, Nb, Ta, and REE concentration relative to zircon from the earlier intrusions. This distinct change in zircon composition coincides with the copper mineralization, suggesting that zircon chemistry can be used as a tool to identify the genetic evolution of a crystallizing magma chamber and potential for mineralization. [ABSTRACT FROM AUTHOR]

The late Cenozoic Anatolian Metallogenic Trend in Turkey is a manifestation of westerly Aegean subduction and easterly Arabian continental collision along the Western Tethyan Orogenic Belt. The 1500 × 200 km late Cenozoic Anatolian magmatism hosts many gold-rich porphyry and epithermal deposits and prospects (~ 27 Moz Au) that formed during the tearing of the Aegean slab and Arabian slab break-off events that initiated at 15 Ma in western Anatolia and 25 Ma in eastern Anatolia. Although the temporal and spatial correlations between slab segmentation, late Cenozoic magmatism, and associated gold-rich porphyry and epithermal mineralization has been intuitively proposed, the genetic relationships between asthenospheric upwelling, subcontinental lithospheric mantle instability, and magma fertility have not been well established. Herein, new geochemical and radiogenic Sr, Nd, and Pb isotope data from Miocene to Pliocene magmatic rocks that are genetically related to porphyry, epithermal, and skarn systems from western, central, and eastern Anatolia are presented and interpreted with previously published geochemical data from late Cenozoic intrusion-related mineral systems throughout Anatolia. The magma fertility of the late Cenozoic post-subduction igneous suites along the late Cenozoic Anatolian Metallogenic Trend is assessed and is best indicated by the SiO2 (61.8 ± 5.5 wt%) content, Sr/Y (> 20) and Ba/Ta ratios (> 428), and (εNd)i values (< 0). Fertile magmatism dominantly resulted from the melting of the metasomatized Anatolian SCLM and was accompanied by amphibole ± clinopyroxene and plagioclase fractionation in the absence of garnet residue as indicated by low (Dy/Yb)N and Eun/Eu* ratios. Magma fertility indicators evolved through time along the late Cenozoic Anatolian Metallogenic Trend. In western Anatolia, fertile magmatism peaked in the middle to late Miocene (15–9 Ma) and was preceded by less-fertile early Miocene magmatism (21–18 Ma) and followed by barren Pliocene to Quaternary, alkaline lavas. The geochemical signatures of mineralized igneous units in central and eastern Anatolia indicate that fertile magmas formed early as regional magmatism evolved towards less hydrous, less oxidized, shallower, and mantle-dominant signature. The reduction of magmatic fertility since the late Miocene throughout Anatolia was caused by the upwelling of hot, dry asthenosphere through the Aegean slab tear and Arabian slab break-off, SCLM instability, and subsequent removal in absence of an over-thickened crust. The spatial migration of slab ruptures and slab gap opening modified mantle fluxes, reduced the SCLM thickness and volume of fusible material, and caused the migration of melting source. Thus, the segmentation of the Southern Neotethyan oceanic slab triggered the metallogenic events along the Anatolian Trend but subsequently contributed to the cessation of production of fertile magma. [ABSTRACT FROM AUTHOR]

This study investigates apatite and anhydrite inclusions in zircon from ore-forming intrusions in the Duolong porphyry Cu-Au deposit, central Tibet (Fig. 2 Geological characteristics (a) and cross sections (b, c) of the Duolong porphyry Cu-Au deposit, central Tibet, showing sample locations (Li et al. [21], [25]) The Duolong magmatic complex evolved from diorite to granodiorite porphyry and quartz diorite porphyry, the hosts of Cu-Au mineralization (Fig. Apatite inclusions ( I n i = 98) in zircon from the granodiorite porphyry and quartz diorite porphyry have F contents of 1.14-2.99 wt%, Cl of 0.16-2.51 wt%, and SO SB 3 sb of 0.04-1.38 wt%, with minor SiO SB 2 sb (0.05-1.39 wt%), MnO (0.12-0.93 wt%), Na SB 2 sb O (0-0.28 wt%), and FeO (0.01-0.64 wt%; Supplementary Table 1). Apatite and anhydrite were randomly enclosed by zircon crystals, which were later hosted in ore-forming porphyries One apatite inclusion coexisting with an anhydrite inclusion in a single zircon grain contains 0.69 wt% SO SB 3 sb with a low I X i SB F sb / I X i SB Cl sb ratio of ~ 1.2 (Fig. [Extracted from the article]

The Kekura gold deposit (76.2 t Au at 8.1 g/t) is situated in Western Chukotka, a region that hosts several Au, Ag, Cu, and Mo deposits and prospects. The Kekura deposit is related to the eponymous granite intrusion that is cut by porphyry dikes. The U-Pb zircon age of one of these dikes is 112 ± 1 Ma (2σ) that corresponds to the latest Aptian/earliest Albian. Both intrusion and dikes are hydrothermally altered and are cut by gold-quartz and molybdenite-quartz veins and stringers. Two molybdenite samples yield Re-Os model ages of 112.5 ± 0.6 and 112.3 ± 0.6 Ma (2σ). These Re-Os ages indicate the close temporal relationship between the molybdenite mineralization and the porphyry dikes. The age of the Kekura mineral system is similar to that of the post-collisional granitic plutons of the Anyui zone spatially scattered, between 140 and 210 km northwest of Kekura. We suggest that this temporal relationship may increase the likelihood of further discoveries of economic gold mineralization related to the currently underexplored Aptian post-collisional magmatic complexes of the Western Chukotka area. [ABSTRACT FROM AUTHOR]

Altar is a large porphyry Cu (Au) deposit located in the Main Cordillera of Argentina, 20 km to the north of the giant Los Pelambres–El Pachón porphyry copper cluster, at the southern portion of the Pampean flat-slab segment of the Andes. Although this region hosts telescoped porphyry-epithermal deposits, the precise temporal relationship between porphyry emplacement, mineralization, cooling, and regional orogenic uplift are still poorly understood. New Re–Os molybdenite ages indicate that Altar orebodies are associated with two magmatic hydrothermal centers: Altar East (11.16 ± 0.06 Ma) and Altar Central (10.38 ± 0.05 Ma) formed at temporally distinct periods. New (U–Th)/He ages from the Early Permian and Late Eocene plutons, and the Middle Miocene subvolcanic stocks associated with Cu–Au mineralization of the Altar region reflect a rapid cooling pulse during the Middle Miocene (15.02 to 10.66 Ma) coeval with a major phase of tectonic shortening and regional uplift. The main pulse of rapid cooling and related tectonic uplift in the Altar region was synchronous with the formation of the hydrothermal systems and resulted in an increased focused metal endowment (Au–Cu grades) due to the telescoping of epithermal mineralization over the rapidly uplifted porphyry system. This 11–10 Ma tectonically triggered exhumation event coincides with the collision of the E-trending segment of the Juan Fernández Ridge with the Peru–Chile trench, at this latitude. Collision and ensuing ridge subduction may have driven a localized pulse of rapid cooling and exhumation of the Main Cordillera that has not been well documented to the north or south of the Altar–Los Pelambres region. [ABSTRACT FROM AUTHOR]

The Zhilingtou polymetallic deposit, South China, provides an excellent opportunity to investigate the magmatic-hydrothermal evolution of the porphyry Mo to epithermal Au–Ag–Pb–Zn ore spectrum. New zircon U–Pb, sphalerite 40Ar/39Ar, and pyrite Rb–Sr ages, together with previous molybdenite Re–Os ages, indicate that the granitic magmatism and Mo–Au–Ag–Pb–Zn mineralization were coeval and cogenetic in the Early Cretaceous (~ 113 Ma). Fluid inclusions and H–O isotope results have established the evolution from an early high-temperature H2O–NaCl magmatic fluid system (Mo mineralization), to a medium-temperature mixed fluid system of magmatic and meteoric water (Au–Ag mineralization), to a peripheral late-stage low-temperature H2O–NaCl meteoric water fluid system (epithermal Au–Ag–Pb–Zn mineralization). Moreover, the sulfur isotopic compositions (δ34S = 2.1–7.8‰) of the sulfide minerals confirm a genetic link to the granitic magma. Lead isotope data from pyrite and the granite–rhyolite porphyries are similar, indicating that they share a common Pb source. The geochronological, geochemical, and isotopic lines of evidences consistently suggest that the porphyry Mo and epithermal Au–Ag–Pb–Zn mineralization formed in one magmatic–hydrothermal system. The porphyry-epithermal mineralization model for Zhilingtou has significant importance for prospecting work in South China, where Mo and associated Pb–Zn–Ag resources are abundant. [ABSTRACT FROM AUTHOR]

The Atlas porphyry Cu–Au deposit is located in central Cebu Island in the Philippines, with a proven mineral reserve of 1420 Mt at 0.45% Cu, 0.24 g/t Au, 0.018 g/t Mo, and 1.8 g/t Ag. It is associated with the Lutopan quartz diorite porphyry stock that was emplaced into the Cretaceous volcano-sedimentary sequences of the Cansi Formation. Two stages of hypogene alteration have been identified at Atlas: stage I quartz–magnetite ± chalcopyrite ± pyrite veins associated with potassic and propylitic alteration and stage II anhydrite–pyrite–chalcopyrite ± specularite veins associated with phyllic alteration. Supergene gypsum veins are also present. Mineralization is mainly associated with the stage I and stage II veins. The Lutopan quartz diorite porphyry yielded a zircon U–Pb age of 108.5 ± 1.6 Ma and is characterized by high Sr/Y (54–69), with the corresponding magma having high oxygen fugacity (avg. ΔFMQ +2.7, avg. Ce4+/Ce3+ of zircon = 439) and H2O concentrations (presence of amphibole and biotite phenocrysts) and low magmatic temperatures (avg. Ti-in-zircon thermometry = 706 °C). The relatively low La/Yb ratios (9–11), listric-shaped normalized REE patterns with weak or absent Eu anomalies, together with zircon εHf(t) values of 3.4 to 10.0, whole-rock ISr values of 0.70373–0.70382, εNd(t) values of 2.4–3.4 and Mg numbers of 49–53 suggest that the Lutopan quartz diorite porphyry was likely derived from partial melting of young lower continental crust or interaction between asthenospheric melts and lower crust melts, that evolved to adakite-like trace element compositions through amphibole fractionation. Stage I veins yielded a pyrite Re–Os isochron age of 110.2 ± 5.6 Ma, making Atlas the only Mesozoic porphyry deposit discovered in the Philippines. [ABSTRACT FROM AUTHOR]

The Golden Mile in the 2.7 Ga Eastern Goldfields Province of the Yilgarn Craton, Western Australia, has produced 385 million tonnes of ore at a head grade of 5.23 g/t gold (1893–2016). Gold-pyrite ore bodies (Fimiston Lodes) trace kilometre-scale shear zone systems centred on the D2 Golden Mile Fault, one of three northwest striking sinistral strike-slip faults segmenting upright D1 folds. The Fimiston shear zones formed as D2a Riedel systems in greenschist-facies (actinolite-albite) tholeiitic rocks, the 700-m-thick Golden Mile Dolerite (GMD) sill and the Paringa Basalt (PB), during left-lateral displacement of up to 12 km on the D2 master faults. Pre-mineralisation granodiorite dykes were emplaced into the D2 shear zones at 2674 ± 6 Ma, and syn-mineralisation diorite porphyries at 2663 ± 11 Ma. The widespread infiltration of hydrothermal fluid generated chlorite-calcite and muscovite-ankerite alteration in the Golden Mile, and paragonite-ankerite-chloritoid alteration southeast of the deposit. Fluid infiltration reactivated the D2 shear zones causing post-porphyry displacement of up to 30 m at principal Fimiston Lodes moving the southwest block down and southeast along lines pitching 20°SE. D3 reverse faulting at the southwest dipping GMD-PB contact of the D1 Kalgoorlie Anticline formed the 1.3-km-long Oroya Shoot during late gold-telluride mineralisation. Syn-mineralisation D3a reverse faulting alternated with periods of sinistral strike-slip (D2c) until ENE-WSW shortening prevailed and was accommodated by barren D3b thrusts. North-striking D4 strike-slip faults of up to 2 km dextral displacement crosscut the Fimiston Lodes and the barren thrusts, and control gold-pyrite quartz vein ore at Mt. Charlotte (2651 ± 9 Ma). [ABSTRACT FROM AUTHOR]

The Tuwu porphyry Cu deposit, located in Eastern Tianshan, NW China, is hosted by a plagiogranite porphyry and Carboniferous Qi'eshan Group volcanic rocks. Based on crosscutting relationships and mineral assemblages, hydrothermal alteration and mineralization processes at Tuwu can be divided into four stages: early propylitic alteration (stage I), porphyry mineralization (stage II), overprinting mineralization (stage III), and post-mineralization (stage IV). The porphyry mineralization stage (stage II) contributed to the majority of the Cu–Mo resource, with Cu mineralization occurring mainly as quartz-chalcopyrite veins. Stage III also produced minor Cu mineralization, characterized by chalcopyrite–anhydrite–chlorite–calcite assemblages. Fluid inclusion (FI) study reveals that stage II is characterized by a high-temperature, high-salinity, highly oxidized, and K-rich H2O–NaCl–CaCl2 fluid. Fluid boiling and mixing likely occurred during the porphyry mineralization stage, leading to the precipitation of chalcopyrite and pyrite. Alteration and mineralization in stage III were derived from a S-rich H2O–NaCl–CaCl fluid, with fluid boiling leading to the precipitation of chalcopyrite. The δ34S values of chalcopyrite from stages II and III are − 0.8–0.6 ‰ and 1.1–1.3 ‰, respectively, suggesting magmatic sources for the ore-forming components of both stages. 40Ar/39Ar dating indicates that stage II likely occurred at 328.1 ± 1.4 Ma, around the age emplacement of the causative plagiogranite porphyry (ca. 337.7–330.3 Ma). We suggest the overprinting mineralization event occurred at ca. 323 Ma, spatially and genetically related to the emplacement of the quartz albite porphyry at 323.6 ± 2.5 Ma. [ABSTRACT FROM AUTHOR]

It has been widely accepted that magmas genetically linked to porphyry (-skarn) Cu (Mo) deposits are commonly oxidized. Recently, using laser ablation-inductively coupled plasma-mass spectrometry (LA-ICP-MS) techniques, zircon Ce4+/Ce3+, CeN/CeN*, EuN/EuN*, and Ce/Nd ratios, and magma ΔFMQ values (departure from the fayalite–magnetite–quartz oxygen buffer) based on zircon trace element compositions, have been used as proxies to quantify magma oxidation state. Here we present the zircon trace element compositions of 13 Mesozoic porphyry (-skarn) Mo deposits in NE China of various sizes to examine the relationship between magma Mo fertility and magma oxidation state. Generally, the studied deposits with > 0.3 Mt Mo have Ce4+/Ce3+ > 100, CeN/CeN* > 100, Ce/Nd > 10, and EuN/EuN* > 0.3, whereas those containing < 0.3 Mt Mo have Ce4+/Ce3+ < 100, CeN/CeN* < 100, Ce/Nd < 10, and EuN/EuN* < 0.3. The calculated magma ΔFMQ values do not show significant correlation with metal tonnage, probably due to the large uncertainties of the estimated ΔFMQ data. Among these proxies, Ce4+/Ce3+ and CeN/CeN* ratios show the strongest correlation with Mo tonnage, followed by Ce/Nd and EuN/EuN*. The above results confirm the previous proposal that zircon Ce and Eu anomalies can represent an intrusion's oxidation state and indicate that the Mo endowment of magmatic-hydrothermal deposits is positively correlated with the magma oxidation state. Compared with Mo-bearing intrusions, the trends for Cu-bearing intrusions are similar but are more complicated, especially for those deposits with > 10 Mt Cu. The findings in this study can be used to evaluate an intrusion's potential to produce Mo mineralization. [ABSTRACT FROM AUTHOR]

Chalcophile element fertility, the chalcophile metal abundance in the source magma, is likely to be a critical factor for the formation of porphyry Cu ± Au deposits. In this study, we provide evidence to support this hypothesis by comparing the platinum group element (PGE) geochemistry of barren and ore-bearing Cu ± Au granitic suites. We report the PGE contents of three barren volcanic and subvolcanic suites from Argentina and Japan and two Cu ± Au bearing suites from Indonesia and Chile. These results are compared with those from previous studies of a porphyry Cu-only subvolcanic suite from Chile and three porphyry Cu-Au-bearing suites from Australia and the USA. The barren suites are depleted in PGE abundances by the time of fluid exsolution (< 0.1 ppb Pd and Pd/Pt < ~ 3), which is attributed to early sulfide saturation in a mid to lower crustal magma chamber. In contrast, the Cu ± Au ore-bearing suites contain at least an order of magnitude higher PGE contents than the barren ones at fluid saturation (up to ~ 10 ppb Pd and Pd/Pt of 0.1–40). They are characterized by late sulfide saturation, which allows both chalcophile elements and sulfur to concentrate by fractional crystallization before volatile saturation. We suggest that plots of Pd/MgO against Pd/Pt for igneous suites can be used to estimate chalcophile element fertility and distinguish between barren, porphyry Cu, and porphyry Cu-Au granitoid systems. The positive correlation of these chalcophile element fertility indicators and ore grades suggests that metal contents in magmas play an important role in controlling ore grade, particularly Au, in porphyry Cu ± Au deposits. [ABSTRACT FROM AUTHOR]

Trace element compositions of magnetite and hematite from 16 well-studied iron oxide–copper–gold (IOCG) and iron oxide apatite (IOA) deposits, combined with partial least squares-discriminant analysis (PLS-DA), were used to investigate the factors controlling the iron oxide chemistry and the links between the chemical composition of iron oxides and hydrothermal processes, as divided by alteration types and IOCG and IOA deposit subtypes. Chemical compositions of iron oxides are controlled by oxygen fugacity, temperature, co-precipitating sulfides, and host rocks. Iron oxides from hematite IOCG deposits show relatively high Nb, Cu, Mo, W, and Sn contents, and can be discriminated from those from magnetite + hematite and magnetite IOA deposits. Magnetite IOCG deposits show a compositional diversity and overlap with the three other types, which may be due to the incremental development of high-temperature Ca–Fe and K–Fe alteration. Iron oxides from the high-temperature Ca–Fe alteration can be discriminated from those from high- and low-temperature K–Fe alteration by higher Mg and V contents. Iron oxides from low-temperature K–Fe alteration can be discriminated from those from high-temperature K–Fe alteration by higher Si, Ca, Zr, W, Nb, and Mo contents. Iron oxides from IOA deposits can be discriminated from those from IOCG deposits by higher Mg, Ti, V, Pb, and Sc contents. The composition of IOCG and IOA iron oxides can be discriminated from those from porphyry Cu, Ni–Cu, and volcanogenic massive sulfide deposits. [ABSTRACT FROM AUTHOR]

The Late Devonian Tsagaan Suvarga deposit (255 Mt at 0.55% Cu, 0.02% Mo) is located on the NW margin of the Tsagaan Suvarga Complex (TSC), which extends ENE over 15 × 10 km and comprises mainly medium-grained equigranular hornblende-biotite quartz monzonite and monzodiorite. Distinct mineralized intrusions are inferred from distribution of Cu-Mo mineralization but are not clearly discernible. The Tsagaan Suvarga Complex is a window within Carboniferous volcanic and sedimentary rocks, and wall rocks to the TSC are not known or exposed in the nearby district. Whole-rock analyses and Sr-Nd isotopes, 87Sr/86Sr0 = 0.7027 to 0.7038 (n = 12) and εNd0 = + 4.26 to + 2.77 (n = 12), show that the granitoids are subduction-related I-type, high K-calc-alkaline to shoshonitic series and derived from a mantle source. They exhibit fractionated light rare earth elements, without depleted Eu and depleted middle heavy rare earth elements and Y, typical of oxidized, fertile porphyry magmatic suites. Early porphyry-style quartz veins include A- and B-type. Molybdenite occurs in monomineralic veins (1-5 mm) or A veins. Copper mineralization occurs mainly as chalcopyrite and subordinate bornite, disseminated and associated with quartz-muscovite veins. Pyrite (vol%) content is less than chalcopyrite and bornite combined. Deep oxidation to about 50 m depth has formed zones of malachite and covellite in late fractures. The most important alteration is actinolite-biotite-chlorite-magnetite replacing hornblende and primary biotite. Quartz-K-feldspar alteration is minor. Late albite replaces primary K-feldspar and enhances sodic rims on plagioclase crystals. Quartz-muscovite (or sericitic alteration) overprints actinolite-biotite and porphyry-type quartz veins. Field observations and petrographic studies suggest that the bulk of the chalcopyrite-bornite mineralization at the Tsagaan Suvarga formed together with coarse muscovite alteration. [ABSTRACT FROM AUTHOR]

The Biely Vrch deposit in the Western Carpathians is assigned to the shallow, sulfide-poor porphyry gold deposit type and has an exceptionally low Cu/Au ratio. According to 3-D geochemical models, there is a limited spatial correlation between Au and Cu due to the primary introduction of gold by a salt melt and Cu by low-density vapor. Despite a rough spatial correlation of gold grades with quartz stockwork intensity, gold is hosted mostly by altered rock, exclusively in native form. Three main gold mineral assemblages were recognized here. In the deepest parts of the system, the K- and Ca-Na silicate gold assemblage is associated with minerals of high-temperature alteration (plagioclase, K-feldspar, actinolite), with gold grades and fineness depending on depth and potassium content of the host rock: K-silicate alteration hosts the lowest fineness gold (~ 914), whereas Ca-Na silicate alteration has the highest (~ 983). The intermediate argillic gold assemblage is the most widespread, with gold hosted mainly by chlorite, illite, smectite, and interstratified illite-chlorite-smectite minerals. The gold fineness is mostly variable (875-990) and inherited from the former gold mineral assemblages. The latest advanced argillic gold assemblage has its gold mostly in kaolinite. The extremely high fineness (~ 994) results from gold remobilization by late-stage aqueous magmatic-hydrothermal fluids. Uncommon bonanza-grade appears where the earlier gold mineral assemblages were further enriched by this remobilized gold. Primary precipitation of gold occurred during ascent and cooling of salt melts at 450 to 309 °C, mostly during retrograde quartz solubility. [ABSTRACT FROM AUTHOR]

The Dalingshang W-Cu deposit is located in the North section of the Dahutang ore field, northern Jiangxi Province, South China. Vein- and breccia-style tungsten-copper mineralization is genetically associated with Mesozoic S-type granitic rocks. Infrared and conventional microthermometric studies of both gangue and ore minerals show that the homogenization temperatures for primary fluid inclusions in wolframite (~ 340 °C) are similar to those in scheelite (~ 330 °C), but about 40 °C higher than those of apatite (~ 300 °C) and generally 70 °C higher than those in coexisting quartz (~ 270 °C). Laser Raman analysis identifies CH4 and N2 without CO2 in fluid inclusions in scheelite and coexisting quartz, while fluid inclusions in quartz of the sulfide stage have variable CO2 content. The ore-forming fluids overall are characterized by high- to medium-temperature, low-salinity, CH4, N2, and/or CO2-bearing aqueous fluids. Chalcopyrite, muscovite, and sphalerite are the most abundant solids recognized in fluid inclusions from different ores. The H-O-S-Pb isotope compositions favor a dominantly magmatic origin for ores and fluids, while some depleted δ34S values (− 14.4 to − 0.9‰) of sulfides from the sulfide stage are most likely produced by an increase of oxygen fugacity, possibly caused by inflow of oxidized meteoric waters. The microthermometric data also indicate that a simple cooling process formed early scheelite and wolframite. However, increasing involvement of meteoric waters and fluid mixing may trigger a successive deposition of base metal sulfides. Fluid-rock interaction was critical for scheelite mineralization as indicated by in-situ LA-ICP-MS analysis of trace elements in scheelite. [ABSTRACT FROM AUTHOR]

Cerro de Pasco (Peru) is known for its large epithermal polymetallic (Zn-Pb-Ag-Cu-Bi) mineralization emplaced at shallow level, a few hundred meters below the paleo-surface, at the border of a large diatreme-dome complex. Porphyry-style veins crosscutting hornfels and magmatic rock clasts are found in the diatreme breccia and in quartz-monzonite porphyry dikes. Such mineralized veins in clasts allow investigation of high-temperature porphyry-style mineralization developed in the deep portions of magmatic-hydrothermal systems. Quartz in porphyry-style veins contains silicate melt inclusions as well as fluid and solid mineral inclusions. Two types of high-temperature (> 600 °C) quartz-molybdenite-(chalcopyrite)-(pyrite) veins are found in the clasts. Early, thin (1-2 mm), and sinuous HT1 veins are crosscut by slightly thicker (up to 2 cm) and more regular HT2 veins. The HT1 vein quartz hosts CO2- and sulfur-rich high-density vapor inclusions. Two subtypes of the HT1 veins have been defined, based on the nature of mineral inclusions hosted in quartz: (i) HT1bt veins with inclusions of K-feldspar, biotite, rutile, and minor titanite and (ii) HT1px veins with inclusions of actinolite, augite, titanite, apatite, and minor rutile. Using an emplacement depth of the veins of between 2 and 3 km (500 to 800 bar), derived from the diatreme breccia architecture and the supposed erosion preceding the diatreme formation, multiple mineral thermobarometers are applied. The data indicate that HT1 veins were formed at temperatures > 700 °C. HT2 veins host assemblages of polyphase brine inclusions, generally coexisting with low-density vapor-rich inclusions, trapped at temperatures around 600 °C. Rhyolitic silicate melt inclusions found in both HT1 and HT2 veins represent melt droplets transported by the ascending hydrothermal fluids. LA-ICP-MS analyses reveal a chemical evolution coherent with the crystallization of an evolved rhyolitic melt. Quartz from both HT1 and HT2 veins also contains secondary, low-temperature (~ 300 °C) brine and aqueous fluid inclusions that record the cooling of the system. Both vein types are locally crosscut and/or reopened by a pre-diatreme polymetallic event consisting of pyrite, sphalerite with “chalcopyrite disease,” galena, chalcopyrite, tetrahedrite-tennantite, and minor quartz. LA-ICP-MS analyses of mineral and high-temperature fluid inclusions hosted in HT1 and HT2 veins and in situ secondary-ion mass spectrometry oxygen isotope analyses of vein quartz indicate a magmatic signature for the mineralizing fluids with no major meteoric water input and allow reconstruction of the source and chemical evolution of fluids that formed these porphyry-style veins as snapshots of the early and deep mineralizations at Cerro de Pasco. This detailed study of the porphyry-type mineralization hosted in clasts offers a unique opportunity to reconstruct the late magmatic and early hydrothermal evolutions of porphyry mineralization underlying the world-class Cerro de Pasco epithermal polymetallic (Zn-Pb-Ag-Cu-Bi) deposit. [ABSTRACT FROM AUTHOR]

Mo-Cu mineralization in the Baituyingzi district of eastern Inner Mongolia occurs within a granitic complex. This paper presents and discusses zircon U-Pb ages and whole-rock geochemical and Sr-Nd-Pb isotopic data from the granitic complex as potential indicators for porphyry Mo fertility. The U-Pb ages indicate that five units of the granitic complex were emplaced between 265.2 ± 0.7 and 246.5 ± 1.0 Ma. Constrained by crosscutting dikes, Mo-Cu mineralization was probably related to the Baituyingzi monzogranite porphyry dated at 248.2 ± 0.64 Ma. The intrusions belong to high-K calc-alkaline to shoshonitic series that are characterized by highly fractionated rare earth element (REE) patterns and strong enrichments of large ion lithophile elements, relative to high-field strength elements. Apart from the ∼246-Ma dike that shows negative εNd ( t) values (−14.9 to −13.1), the intrusions have εNd( t) values ranging from −3.9 to 1.0, relatively young depleted mantle model ages (811 to 1183 Ma), Pb/Pb of 18.137-18.335, and Pb/Pb of 15.591-15.625, which are consistent with a juvenile lower crustal origin. Among the intrusions, the ∼248-Ma porphyry and the ∼246-Ma dike show adakite-like characteristics (e.g., Sr/Y = 44.9-185) and listric-shaped REE patterns that indicate amphibole fractionation and a hydrous magma source. However, the porphyry exhibits a higher differentiation index (81.4-91.5) and a steeper REE profile (e.g., La/Yb = 25.6-87.0) than those of the ∼246-Ma dike, which suggests that it is highly differentiated. We propose that the complex was generated by the partial melting of juvenile mafic lower crust (containing minor old crustal relicts) that was triggered by collision between the North China Craton and Siberian Craton. As indicated by the Th/Nb, Th/Yb, Ba/Th, and Ba/La ratios of the intrusions, the crust may have been derived from the melting of the fertile mantle wedge that was metasomatized by various amounts of slab-derived fluids or melts due to earlier subduction and was heterogeneous in terms of water, Cu, Mo, and S contents and possible oxidation state. The fertility of the porphyry was likely associated with the addition of earlier subduction-related slab melts to the magma source (leading to a hydrous and possible high oxidation state) and the long-time (∼20 Ma) collision tectonic setting in which it formed (resulting in a highly differentiated state). [ABSTRACT FROM AUTHOR]