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The sources of fluids and metals in porphyry systems of continental-collision settings are poorly constrained. Mercury isotopes display unique mass-independent fractionation (expressed as Δ199Hg) and may provide important constraints on metal and volatile sources given that Hg is a highly volatile metal. Here, we report Hg isotope data on ore-forming porphyries, barren magmatic rocks, and mantle-derived mafic magmas from southern Tibet. The fertile porphyries and coeval mafic magmas display mainly positive Δ199Hg values (up to +0.25 per mil), while Δ199Hg values in barren magmatic rocks and mafic magmas are largely negative (-0.54 to 0.00 per mil). The positive Δ199Hg values observed here are consistent with seawater and marine sediments, suggesting that the ultimate source of fluids involved in the genesis of post-subduction porphyry copper deposits was the mantle lithosphere metasomatized by previous oceanic plate subduction. Our Hg isotope data provide an alternative view to current metallogenetic models on collisional porphyry systems that focus on melting of the lower continental crust. [ABSTRACT FROM AUTHOR]

Porphyry-type Cu ± Au ± Mo deposits form in the upper (ca. 2-5 km deep) parts of large, long-lived magmatic-hydrothermal systems in which mineralising fluids are thought to be derived from mid-to shallow-crustal magma chambers. Increasingly, however, magmatic systems are viewed as consisting of mush with minor and transient lenses of magma, with mush being a variably packed framework of crystals with interstitial melt and magmatic volatile phase (MVP). In this context, questions remain as to the source (mainly depth) and mechanisms of transport and focussing of the vast volumes of fluids required for shallow level porphyry-type mineralisation. Even more problematic is a paucity of first-order textural evidence for the presence of mush in magmatic-hydrothermal systems, including those which host porphyry-type deposits. To address this, we have studied the aplitic porphyry cupola of the Saginaw Hill magmatic system, Tuscon, Arizona, United States, where magmatic-hydrothermal features are exceptionally well exposed, including a massive silica cap, quartz unidirectional solidification textures (USTs), stockworks of multiple generations of variably mineralised quartz veins and mineralised miarolitic cavities. From field-to micro-scale textural and geochemical studies, particularly observations of vermiform quartz between earlier generations of magmatic quartz and feldspar, we evidence the development of fluid pathways through mush at the magmatic-hydrothermal transition. These are shown to connect and provide fluids and ore constituents to the mineralised miarolitic cavities and early quartz vein stockworks. We suggest that this process should be considered in all new genetic, exploration and numerical models for porphyry and similar types of magmatic-hydrothermal ore-deposits. [ABSTRACT FROM AUTHOR]

Porphyry Cu, and porphyry Cu–Au deposits, are associated with arc magmatism and their ore-forming systems generally follow the magmatic evolution of typical arcs. However, most arc magmas are barren and giant economic porphyry Cu ± Au deposits are rare. In this study, we model variations in rare earth element concentrations in evolving arc magmas and giant porphyry Cu ± Au systems to quantify the percentage of the fractionating minerals required to produce the observed changes. We find that, during the andesitic stage of fractionation, ore-forming systems in thick crusts fractionate ~35% more amphibole than an average of thick arc magma systems (the thick-crust reference suite) and that ore-forming systems in thin crusts fractionate twice as much amphibole as their equivalent thin-arc magma reference suite. Thick-crust ore-forming suites also fractionate ~50% less plagioclase, and thin-crust ore systems ~40% less plagioclase, than their associated reference suites during the same andesitic stage of fractionation. Taken together, these observations imply that ore-producing magmas are appreciably wetter than their associated barren reference suites. Our modeling also shows that ~80% more amphibole is required to reproduce the andesite stage of fractionation in the thick-crust reference suite than in its thin-crust equivalent, suggesting that magmas produced under thick crusts are wetter than those produced under thin crusts. On the other hand, the chalcophile element contents of the thick- and thin-crust ore-forming systems are similar to and higher than those of the thick- and thin-crust reference suites, respectively. Therefore, we suggest that the high water content plays a critical role in the formation of giant porphyry Cu ore in thick crusts, whereas both high chalcophile contents and high water contents are required to form giant porphyry Cu–Au deposits in thin crusts. The high fraction of amphibole fractionation in giant economic porphyry suites, compared with their relevant reference suites, results in lower Y in the ore-associated suites and this difference increases with fractionation. As a consequence, plots of Y against MgO can be used to identify porphyries that have economic potential and are preferred to Sr/Y plots because they are less affected by the intense alteration associated with giant porphyry Cu ± Au deposits. [ABSTRACT FROM AUTHOR]

Quartz is widely distributed in various magmatic-hydrothermal systems and shows variable textures and trace element contents in multiple generations, enabling quartz to serve as a robust tracer for monitoring hydrothermal fluid evolution. This study demonstrates that integrated high-resolution SEM-CL textures and trace element data of quartz can be used to constrain physicochemical fluid conditions and trace the genesis of quartz in porphyry ore-forming systems. The Bilihe deposit is a gold-only porphyry deposit located in the Central Asian orogenic belt, NE China. Four quartz generations were distinguished following a temporal sequence from early-stage dendritic quartz, unidirectional solidification textured quartz (UST quartz), gray banded vein quartz (BQ), to late-stage white calcite vein quartz (CQ), with the Au precipitation being mostly related to dendritic quartz, UST quartz, and BQ. The well-preserved dendritic quartz with sector-zoned CL intensities and euhedral oscillatory growth zones crystallized rapidly during the late magmatic stage. The relatively low Al contents of dendritic quartz were interpreted to be related to contemporaneous feldspar or mica crystallization, while the high-Ti contents indicate high-crystallization temperatures (~750 °C). The comb-layered UST quartz displays heterogeneous, patchy luminescence with weak zoning, hosts coeval melt and fluid inclusions, and retains the chemical characteristics of magmatic dendritic quartz. High-Ti and low-Al contents of UST quartz suggest a formation at relatively high temperatures (~700 °C) and high-pH conditions. Three sub-types can be defined for hydrothermal BQ (BQ1, BQ2, and BQ3) based on contrasting CL features and trace element contents. The Al contents increase from BQ1 to BQ2 followed by a drop in BQ3, corresponding to an initial decrease and subsequent increase in fluid acidity. Temperature estimates of BQ decrease from BQ1 (635 °C) to BQ3 (575 °C), which may, however, be disturbed by high growth rates and/or high-TiO2 activities. The CQ typically displays a CL-bright core and CL-dark rim with oscillating CL intensities and is characterized by the lowest Ti and highest Al, Li, and Sb contents compared to the other quartz types, which suggests a deposition from more acidic and lower temperature fluids (~250 °C). Trace element patterns indicate that a coupled Si4+ ↔ (Al3+) + (K+) element exchange vector is applicable to dendritic quartz, UST quartz, and BQ. By contrast, charge-compensated cation substitution of Si4+ ↔ (Al3+, Sb3+) + (Li+, Rb+) is favored for CQ. The comparison with compiled trace element data of quartz from other porphyry Au, Cu, and Mo deposits worldwide suggests that Ti, Al, Li, K, and Ge concentrations, as well as Al/Ti and Ge/Ti ratios, have the potential to discriminate the metal fertility of porphyry mineralization. [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]

Copyright of Geology & Exploration is the property of Geology & Exploration Editorial Office and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

The Chagai belt to the north of the Afghan block and the east of the Iranian block in the western part of Pakistan is known for occurrence of Oligocene to Miocene calc‐alkaline magmatic belt. The present study discusses the characteristics of episodic magmatic activities that contributed to mineralization for the Reko Diq porphyry complex in the western part of the Chagai belt. U–Pb dating of zircons from volcanic rocks of the Reko Diq porphyry complex yielded ages of 25.8 ± 1.8 and 12.29 ± 0.44 Ma for two phases of magmatic crystallization. Geochemical analyses of whole‐rock rhyolite and dacite indicate that the rock units are peraluminous calc‐alkaline, derived from Andean‐type subduction. The magma was formed due to partial melting of the thickened mafic lower crust in a continental arc setting in relation to the subduction of the Neotethys along the Makran subduction zone. The abundance of zircons, Hf, REE, U/Pb and Th indicates high degrees of magmatic evolution. Moreover, the Sr and Nd isotopic data indicate the fractional contribution of depleted N‐MORB mantle to the Reko Diq magmas through bulk mixing with magmas derived from the lower continental crust. Short‐lived magmatic systems repeated magma injection, and various episodes of hydrothermal fluid flow have led to the formation of porphyry mineralization. Emplacement of the Reko Diq porphyry complex and related Cu–Au mineralization is associated with a series of tectonic–magmatic events at different episodes of the Oligocene–Miocene times. [ABSTRACT FROM AUTHOR]

High sulphidation (HS) mineralization and associated advanced argillic alteration have been intersected by three drill holes below the Grasberg porphyry Cu-Au deposit, known as the Gajah Tidur prospect. The prospect is located between 1,500-2,750 m level, in Grasberg District, Papua, Indonesia. The holes are of KL98-10-21, KL98-10-22, and GRD39-08 which intersected 3.4 Ma Gajah Tidur monzonite, Grasberg Igneous Complex, the wall rocks of Kembelangan, and New Guinea Limestone Group. This research aims to determine the characteristics of high sulphidation mineralization associated with advanced argillic alteration at Gajah Tidur. Petrographic, XRD, SEM, fluid inclusion, and XRF (geochemical) analyses were applied to identify the mineralogy, geochemistry, and ore fluid properties. The major element plots show a differentiated intrusion. The alteration consists of potassic materials composed of biotite and K-feldspar, overprinted by phyllic and advanced argillic ones typified by alunite, pyrophyllite, and kaolinite. The high sulphidation mineralization characterized by pyrite-covellite, chalcopyrite-chalcocite, enargite, and digenite is also present. Fluid inclusion homogenization temperature of mineralized quartz vein ranges from 393 to 542°C, indicating a magmatic fluid origin predominantly. Two distinct porphyry systems, consisting of the Gajah Tidur Cu-Mo and the Main Grasberg Cu-Au porphyry systems are emplaced at the Gajah Tidur level. Advanced argillic is less intense compared to a pervasive phyllic alteration, overprinting the stockwork and surrounding rocks, emplaced at the upper part of quartz stockwork. It is possibly associated with a late stage of Gajah Tidur porphyry hydrothermal fluids which became cooler and highly acidic. Similar to other porphyry systems such as Oyu Tolgoi in Mongolia, the Gajah Tidur porphyry did not have its hydrothermal fluid ascent to the surface to form lithocap. Instead, the ascending fluids cooled at shallower depths resulting in the formation of advanced argillic alteration. [ABSTRACT FROM AUTHOR]

The Pulang copper deposit, formed in the Late Triassic, is the largest porphyry Cu-Mo-Au deposit in the eastern Tethys, and its genetic type and mineralization potential have received widespread attention. Identifying the characteristics of ore-forming fluids and the sources of ore-forming materials in the deep and peripheral ore bodies of Pulang is particularly important for constructing a complete porphyry copper mineralization system. Based on detailed core logging and geological observations, this article provides extensive petrographic, fluid inclusion micro-thermometry, laser Raman spectroscopy, and H-O-S isotope data on the veins of the main mineralization stage (B veins) in the first mining area and eastern ore section of the Pulang porphyry copper deposit. The genetic correlation between the eastern ore section and the first mining area is clarified, and their mineralization potential is inferred. The results indicate that the deep vein bodies in the first mining area exhibit multi-stage characteristics, and the fluid in B veins exhibits both high-temperature and salinity characteristics. The magma-derived early ore-forming fluids underwent processes such as boiling and experienced immiscibility during meteoric water mixing, which could be the primary mechanism of the precipitation of Cu, Mo, Au, and other metals. The outer eastern ore section is located in a medium-to-low-temperature hydrothermal mineralization zone far from the mineralization center. This outer eastern ore section is a distant part of the magmatic–hydrothermal system of the first mining area. [ABSTRACT FROM AUTHOR]

Copper–gold porphyry deposits are the world's main source of copper and a significant source of gold. They consist of vein networks and their surrounding alteration zones. Commonly the deposits are centred on narrow intrusions (stocks), but calling these deposits 'porphyries' is unjustified because the name carries little descriptive or genetic value. Extensional veins were formed by hydraulic fracturing of the stocks, at depths where open spaces could not be maintained and where fluid pressure approaches lithostatic pressure. The post-crystallisation timing of the veins is important because it indicates that the host stocks could not have been the direct sources of either metals or ore-forming fluids. In the traditional magmatic model, precursor batholiths, lying at depth, are inferred to be the sources of the Cu and Au in the overlying host stocks. In this model, the batholiths are assumed to have crystallised and produced the mineralising aqueous fluids, Cu and Au. However, in many porphyry deposits, the concept of metal and fluid supply from deeper batholiths is problematic. Neither Cu nor Au is strongly enriched during the crystallisation of silicate magmas, and although hypersaline fluids are a characteristic of Cu–Au porphyry deposits globally, the source of the Cl remains unconstrained. There is little evidence that silicate magmas can release such Cl-rich fluids, and it remains unexplained how elevated levels of Cl may be achieved in a silicate magma. Therefore, the starting assumption that these deposits formed predominantly from magmatic sources and processes is questioned. This study has selectively focused on the roles of rheology, rock mechanics, vein control, metal-enrichment processes and the sources of Cl. Non-magmatic processes may be enough to facilitate strong partitioning of Cu and Au into high-temperature, oxidising, high-salinity, hydrothermal fluids to form Cu–Au porphyry deposits. Mineralised quartz veins were introduced in fluids during hydraulic fracturing of their host intrusions when these stocks were brittle and had cooled significantly below their solidus temperatures. The porphyry intrusions hosting Cu–Au (copper–gold) mineralisation were not the direct sources of either the fluids or the metals. The sources of Cu and Au included large volumes of surrounding and underlying rocks up to kilometres from the sites of deposition. Cu and Au do not become strongly concentrated during crystal fractionation in evolving silicate magmas. Unaltered igneous rocks have relatively low Cl contents, and experiments suggest low Cl solubilities in granitic to granodioritic magmas. It is highly unlikely that all the Cl required for metal complexing and transport was available from within silicate magmas. [ABSTRACT FROM AUTHOR]

The Hongyuan porphyry Mo–Cu deposit (PMCD) is a rare example of a "reduced" deposit, in contrast to classical oxidized porphyry Cu or Mo–Cu deposits. It is characterized by an ilmenite–series I–type felsic granitoid intrusion, reduced ore‐forming fluids with methane‐rich fluid inclusions, and widely distributed primary pyrrhotite. Mo–Cu mineralization in the Hongyuan PMCD occurs as disseminated in porphyry, granular in miarolitic cavity, and vein‐type in the quartz vein. These three types of mineralization are generally produced in the late magmatic period, magmatic‐hydrothermal transition period, and hydrothermal period, respectively. Molybdenite from miarolitic cavities shows a greater contribution from mantle fluid, as evidenced by mantle He proportions of 37.6%–16.8%. Molybdenite in quartz veins has relatively lower mantle He proportions of 1.63%–10.5%, indicating a predominantly crustal fluid source. The 3He/4He variations of these two groups of molybdenite illustrate an increasing input of crustal fluid during the magmatic to hydrothermal transition. Molybdenite samples from miarolitic cavities and quartz veins yield a Re‐Os model age of 300.5 ± 3.7 Ma, which is consistent with the U–Pb ages of zircons in the wallrock porphyries (300–302 Ma). This further indicates simultaneous diagenesis accompanied by mineralization. The Sr–Nd isotopic compositions (initial 87Sr/86Sr: 0.703404–0.703552; initial 143Nd/144Nd: 0.512585–0.512655; εNd[t]: +6.56 to +7.90) and young T2DM model ages (421–531 Ma) of the Hongyuan porphyries suggest that these rocks were derived from partial melting of the basaltic lower crust. We propose that mantle‐derived fluids rose up and mixed with fluids from the lower crust under an extensional tectonic setting, forming mantle‐like Sr–Nd–He–Ar isotopic compositions. The pre‐mineralization stage of the Hongyuan reduced PMCD is marked by quartz‐molybdenite ± K‐feldspar ± pyrite veins or veinlets and miarolitic cavities in the intensively potassic alteration zone. These veins formed at high temperatures (400–476°C) and high salinities (47.5–56.6 wt.%). The syn‐mineralization stage is the main metallogenic stage represented by numerous quartz‐molybdenite ± pyrrhotite veins associated with moderate to high temperatures (248°C–424°C) and low to high salinities (1.57–50.1 wt.%). The post‐mineralization stage is characterized by low temperatures (104–270°C) and low salinities (0.35–8.81 wt.%). Fluid immiscibility, mixing with meteoric water, ore fluid‐wall rock interactions, and decreasing temperature and salinity have played important roles during molybdenum mineralization. [ABSTRACT FROM AUTHOR]

The statistical modeling with ILR-RPCA-back CLR has two problems when dealing with the closure effect of geochemical data. Firstly, after performing isometric logratio (ilr) transformation, robust principal component analysis (RPCA) is employed for processing. The double-plot diagram illustrates that the element sequence transformation occurs in the first and second principal components, while the unique principal component remains unattainable. Secondly, by transforming both the score and load into the centered logratio (CLR) space using the U matrix, it is possible to obtain a score result that corresponds to the original order of elements according to the CLR = ILR·U formula. However, for obtaining a load result that corresponds to the original order of elements, an alternative formula "CLR = UT·ILR" must be used instead. In order to determine the optimal element assemblage for porphyry copper deposits, this study conducted statistical analysis on mineral assemblages from discovered deposits in the Gangdese metallogenic belt and identified Cu, Mo, Au, Ag, W, and Bi as key elements associated with porphyry copper deposits. Subsequently, by analyzing the singularities of the composite elements, the spatial overlay of the combined element is carried out, and concentration-area (C-A) fractal filtering is applied to identify the anomaly and background areas. To facilitate comparison, we conducted an analysis of various mineral and ore deposit types, revealing the following findings: (1) Combination elements exhibit superior recognition capability than single elements in porphyry copper deposits; (2) Skarn-type copper deposits unrelated to porphyry show a high degree of dissimilarity compared to those related to porphyry; (3) this method offers advantages over the single element method in evaluating porphyry gold deposits by reducing anomaly levels and initial investment during the evaluation stage for porphyry copper anomalies; (4) However, this method has limited ability in distinguishing between porphyry copper and molybdenum deposits. [ABSTRACT FROM AUTHOR]

The Lower Urgen molybdenum deposit (44,856 t Mo @ 0.141%), situated in the northern Great Xing'an Range, is a newly discovered porphyry molybdenum deposit. Mineralization is characterized by veinlet-disseminated- and vein-type quartz–sulfide orebodies primarily occurring in the cupola of the Early Cretaceous granite porphyry stock. In this study, we present a detailed description of the ore geology, molybdenite Re-Os dating, H-O-S-Pb isotopic compositions, and fluid inclusion (FI) analyses including petrography, laser Raman, and microthermometry to precisely constrain the timing of ore formation, the origin of ore-forming fluids and materials, as well as the metal precipitation mechanism. Molybdenite Re-Os dating yielded two model ages of 141.2 ± 1.5 and 147.7 ± 1.7 Ma, coeval with the regional Late Jurassic–Early Cretaceous molybdenum metallogenesis. The hydrothermal process can be divided into three stages: the quartz–molybdenite(–pyrite) stage, quartz–polymetallic sulfide stage, and quartz–carbonate stage. Four types of FIs were distinguished for quartz, including two-phase liquid-rich (L-type), saline (S-type), CO2-rich (C1-type), and CO2-bearing (C2-type) FIs. Microthermometric data showed that the homogenization temperatures and salinities from the early to late stages were 240–430 °C, 5.0–11.9, and 30.1–50.8 wt% NaCl equiv.; 180–280 °C and 3.0–9.1 wt% NaCl equiv.; and 120–220 °C and 0.2–7.9 wt% NaCl equiv., respectively, suggesting a decreasing trend. H-O isotopic compositions indicate that the ore-forming fluids were initially of magmatic origin with the increasing incorporation of meteoric water. S-Pb isotopic compositions indicate that the ore-forming materials originated from granitic magmas, and the mineralization is genetically related to the ore-bearing granite porphyry stock in the deposit. Fluid immiscibility and fluid–rock interaction are collectively responsible for the massive deposition of molybdenite in stage 1, whereas fluid mixing and immiscibility played a critical role in the deposition of polymetallic sulfide in stage 2. [ABSTRACT FROM AUTHOR]

Porphyry ore deposits are the source of much of the copper, molybdenum, gold and silver. Porphyry hydrothermal systems typically form in magmatic arcs above subduction zones. In this article, some key factors that may be involved in the formation of the Pishtene porphyry deposit in Western Srednogorie are outlined. The first process is the generation of magma in sub-arc mantle and enrichment of metals, water and other fluids. Next stage is a cyclic crystal fractionation in deep crustal magma chamber. There are a lot of other factors, such as a sulphide saturation, metal partitioning, precipitation of ore minerals, magmatic-hydrothermal evolution, erosional and weathering processes, but they are not discussed in this study. [ABSTRACT FROM AUTHOR]

A study of both in situ and detrital gold from different deposit types in British Columbia was undertaken to establish deposit-specific compositional characteristics in terms of alloy composition and suites of mineral inclusions. The study is based on 11,840 particles from 160 localities in which nine gold deposit types are represented, although there is a strong bias towards gold of orogenic, low-sulphidation epithermal, and alkalic porphyry origin. In general, Ag values in gold alloys are not a powerful discriminator for deposit type, but minor metals may prove useful where detectable, e.g., Cu in gold from ultramafic associations and Pd and Hg in gold from alkalic porphyry systems. The characterization of inclusion suites is far more illuminating, as they correlate strongly with the mineralogy of auriferous ores from different deposit types. This outcome has confirmed the validity of designing an indicator methodology based on inclusion suites and has permitted the prediction of inclusion suites for gold from other deposit types where data are more scarce. The compositional templates generated in the study were applied to identify the source deposit type(s) of gold from 41 localities (a total of 2916 detrital gold particles) where gold genesis was previously unknown. [ABSTRACT FROM AUTHOR]

We constrain the magma sources of representative post‐collisional ore‐associated and barren suites in the Sanjiang metallogenic belt, Southwest China. The ore‐associated suites generally have higher Mg# and Cr and Ni contents than the crustal melts. Also, they show wide ranges of whole‐rock Nd and zircon Hf isotopes that are similar to the subduction‐modified mantle‐derived alkaline volcanic rocks in the region. Combing with the geochemical model, we suggest that the ore‐associated suites dominantly originated from partial melts of subduction‐metasomatised mantle by fractional crystallisation. In contrast, the barren suites are mainly characterised by low Mg# and Cr and Ni contents that are comparable to the crustal melts and they have enriched whole‐rock Nd and zircon Hf isotopes, indicating a metasomatised lower crustal origin. The different magma sources play an important role in controlling the fertility of contemporary ore‐associated and barren magmatic suites during post‐collisional porphyry ore formation. [ABSTRACT FROM AUTHOR]

The Beiya giant porphyry Au deposit is the largest Cenozoic Au deposit in the Jinshajiang Cu–Mo–Au metallogenic belt. Many granite porphyries of ~36 Ma were exposed in the Beiya deposit, including the Wandongshan (WDS) and Hongnitang monzogranite porphyries (HNT–MPs) with economically important Au metal resources, the uneconomic WDS biotite MP, and Putaishan granite porphyry (GP), and subeconomic MPs at Nandaping (NDP) and Matouwan (MTW) prospects. To reveal the fundamental factors that lead to the different fertility of these granitic porphyries, this study uses the biotite and zircon geochemical compositions to evaluate their petrogenetic and magmatic conditions (e.g., F content, pressure, fO2). The results show that biotites from economic WDS and HNT–MPs exhibit moderate F contents (0.85%–2.16%), low n(FeT)/n(FeT + Mg) ratios (average of 0.36), and shallow emplacement depths of 0.19–1.76 km. In contrast, the uneconomic granite porphyries are characterized by variable F contents (0.17%–2.75%), high n(FeT)/n(FeT + Mg) ratios (average of 0.43), and deep emplacement depths of 2.76 to 5.02 km. Moreover, the economic WDS and HNT–MPs display higher average zircon fO2 (ΔFMQ [fayalite–magnetite–quartz] of +0.88) than uneconomic granite porphyries (ΔFMQ of −0.19), further confirming a higher fO2 of the economic granitic porphyries. These features indicate that magmatic fO2 is a critical factor controlling Cu–Au mineralization at the Beiya Au deposit. In comparison with the economic WDS and HNT–MPs, the subeconomic MPs in the MTW and NDP prospects exhibit higher average biotite n(FeT)/n(FeT + Mg) ratios of 0.47 and 0.45, and lower average zircon ΔFMQ of −0.05 and −0.23, suggesting lower magmatic fO2 and thus have relatively weak potentials to form Cu–Au mineralization. Notably, the economic WDS and HNT–MPs have higher biotite XMg ratios than those of the subeconomic and uneconomic granitic porphyries, indicating that the economic MPs were formed by the partial melting of mixed lower crustal materials with more mantle‐derived materials. Therefore, the addition of mantle‐derived materials played an important role in determining the fO2 of the granitic porphyry, thus primarily controlling its fertility of Cu–Au mineralization. [ABSTRACT FROM AUTHOR]

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The calculated ore-bearing coefficient in the Bunardzik ore body was 0.82%, meaning that within the ore body boundaries only 18% of the mass is not mineralized somehow, which is highly compatible with the remaining three ore bodies within the Buchim porphyry copper mine. The calculated value of the variation coefficient (V) has shown a value of 54% that is in the range of 43-100%, which displays that this ore body belongs to the third group of ore bodies with uneven mineralization. Average copper, gold and silver concentrations were determined as 0.30% Cu, 0.35 g/t Au and 1.0 g/t Ag, respectively. Minimal economic content (MEC) within the Bunardzik ore body, as a representation of this kind of mineralization, was determined as 0.2099% Cu. In a similar manner was calculated the lowest copper boundary (cutoff grade), which has shown a value of 0.1399% Cu thus allowing a certain decrease in the contents of the exploited ore. Also, the so called copper monometal values were calculated, which included the influence of the present gold and silver in the ore. The calculated copper monometal was set at relatively fair 0.399% Cu that represents solid mainstay for exploitation of copper in these low percentage ores. Thee calculated ore reserves in this particular ore body were 24 042 751 t of ore with 0.257% Cu, 0.35 g/t Au and 0.91 g/t Ag and increased mine life for additional 4.4 years. [ABSTRACT FROM AUTHOR]

The Bangbule skarn lead‐zinc (Pb‐Zn) deposit (>1 Mt Zn + Pb) is located in the western Nyainqentanglha polymetallic metallogenetic belt, central Tibet. Lenticular orebodies are all hosted in skarn and developed in the contact zone between the quartz porphyry and carbonate strata of the mid Paleozoic Middle to Upper Chaguoluoma Formation as well as in carbonate and sandstone beds of the Upper Paleozoic Laga Formation. As a newly discovered skarn deposit, the geological background and metallogenesis of this deposit remain poorly understood. Detailed petrological, geochemical and geochronological data of the ore‐related quartz porphyry, helps constrain the mineralization age and contributes to discussion on the ore genesis of the Bangbule deposit. Both endoskarn and exoskarn are identified in the Bangbule deposit. From quartz porphyry to carbonate formation, the exoskarn is zoned from proximal garnet skarn to distal pyroxene skarn. Zircon U‐Pb dating results show that the quartz porphyry formed at 73.9 ± 0.8 Ma. Geochemical analysis results show that the quartz porphyry has high contents of SiO2 (71.40–74.94 wt%) and K2O + Na2O (3.76–8.46 wt%) with A/CNK values of 0.69 to 1.06. Besides, the quartz porphyry is enriched in large ion lithophile elements (LILEs) and light rare earth elements (LREEs) and have low εNd(t) (from –8.25 to –8.19) and high initial (87Sr/86Sr)i values (0.713611–0.714478). Major, trace elements and whole‐rock F concentration analysis results from the endoskarn samples show higher TFe2O3, MgO, CaO, Pb + Zn, W, Sn, Mo and F etc., and lower alkalis (K2O, Na2O, Sr and Ba) than those of fresh quartz porphyry, indicating that the early ore‐forming fluids were an Ca‐Fe‐F‐enriched fluid. Massive ore in the proximal skarn might be related to the high F content in the magma, which lowered the solidus temperature of the quartz porphyry magma and caused a lower temperature of the ore‐forming fluids, as well as facilitating the precipitation of sphalerite and galena. Based on the geochemical characteristics presented in this study, we propose that the ore‐related quartz porphyry was formed by partial melting of crust materials with some juvenile crustal component input. The partial melting of the middle‐upper crust after the initial enrichment of lead and zinc elements are important for the formation of Pb‐Zn deposits. The case study of the Bangbule deposit has proven that there is still a crust‐derived magmatic source region in the western segment of the central Lhasa terrane. Therefore, there is still great potential for Pb‐Zn mineralization and Pb‐Zn exploration. [ABSTRACT FROM AUTHOR]

The magmatic process within upper crust encompasses various contents such as the transition between magmatic and hydrothermal systems and changes in oxygen fugacity (ƒO2), which ultimately play key roles in the formation of porphyry Cu deposits (PCDs). However, tracing these magmatic processes, especially in porphyry systems, is not an easy task. This study reported the detailed process of magmatic fluid exsolution and systematical variation of magmatic ƒO2 within the upper crust of a Tongchang–Chang'anchong porphyry Cu deposit, based on detailed investigations of mineral crystallization sequences and compositional features of the minerals in the fertile porphyries. Results indicate that the fertile porphyries show a high initial ƒO2, with ΔFMQ ≥ +3.0 (ΔFMQ is the deviation of logƒO2 from the fayalite–magnetite–quartz (FMQ) buffer). The magmatic ƒO2 (ΔFMQ) continued to decrease to ~+2 until fluid exsolution occurred at ~790 °C due to wall-rock contamination. The magmatic fluid exsolution process caused a temporary increase in the ƒO2 (to ΔFMQ = ~+3.4). The high magmatic ƒO2 during this process (790–750 °C) resulted in a higher content of ore-forming materials in the exsolved magmatic fluid. When the temperature dropped below 750 °C, the magmatic ƒO2 began to continuously decrease and eventually reached ΔFMQ = ~+0.6. The lower magmatic ƒO2 hindered the further migration of ore-forming materials through the exsolved fluid during this process (< 750 °C). Results of this study indicate that the initial magma during the upper crustal magmatic process of PCDs generally has a high ƒO2, and the contamination of reduced components can significantly decrease the magmatic ƒO2. The early magmatic fluid exsolution process can maintain a high magmatic ƒO2 condition, thereby efficiently extracting ore-forming minerals and producing ore-forming fluids, which is the key to the formation of PCDs. The latter continuous decrease in magmatic ƒO2 during the fluid exsolution process may be the reason preventing the Tongchang–Chang'anchong porphyry Cu deposit to form a giant PCD. [ABSTRACT FROM AUTHOR]

Egypt's mineral resources are an effective means of raising the country's income. Consequently, searching for deep subsurface ore deposits is essential. In this study, we map the subsurface structure and the occurrence of related gold-ore mineralization deposits in ophiolitic-assemblage rocks around the Wadi El-Saqia area in the Central Eastern Desert of Egypt. Our approach combines airborne geophysical data (aeromagnetic mapping) and geochemical analyses. We enhanced the aeromagnetic data and interpreted them using edge-detection methods, such as the first-order vertical derivative (FVD), the analytic signal (AS), the total horizontal derivative (THD), the tilt derivative (TD), the tilt angle (TA), the theta map, both grid and porphyry analyses from the Centre for Exploration Targeting (CET), and Euler deconvolution (ED) techniques. Utilizing these methods, we located the main structural lineaments/contacts that control the distribution of hydrothermal alteration zones. In addition, our geochemical analyses use the mineral chemistry of pyroxene and plagioclase to describe their tectonic and magmatic evolution. The airborne geophysical results revealed that NW–SE, NE–SW, N–S, and E–W structural orientations are prevalent in the studied area, with depths ranging from less than 50 m to about 600 m. To validate the findings, we carried out geochemical sampling, which indicates that pyrite, galena, pyrrhotite, and electrum contain good percentages of gold (ranging from 0.01–0.09 wt%, 0.03–0.1 wt%, 0.12–0.14 wt%, and 53.55–55.01 wt%, respectively). In this study, we were thus able to find preferred locations for gold mineralization, which highlights the value of combining aeromagnetic and geochemical data for mineral exploration. [ABSTRACT FROM AUTHOR]

The Shuangqishan Au deposit (>15 t) is located in the Dehua‐Youxi‐Yongtai goldfield of the southeastern Cathaysia Block, South China. There are three stages of granites in the Shuangqishan Au deposit, the pre‐mineralization granite porphyry formed in the Middle Jurassic (~166.0 ± 0.8 Ma), the metallogenic granite porphyry and monzonite porphyry formed in the late stage of the Late Jurassic (153–151 Ma), the post‐mineralization granites (granite porphyry, the masanophyre, the dioritic porphyrite) formed in the Early Cretaceous (129.0–120.0 Ma). All rocks are characterized by high‐K calc‐alkaline and shoshonities series, the per‐mineralization granites are enriched in Rb, Th, K, Zr, and Hf, depleted in Ba, P, and Ti, significant negative Eu anomaly and distinctly tetrad effect with highly fractionated I‐type granitoids characteristics. The metallogenic granites and the post‐mineralization granite porphyry are enriched in K, Rb, Th, Ce, Zr, Hf, and Y, enriched in LREE, strongly depleted in Sr, Ba Ta, P, Ti, have moderate negative Eu anomalies with I‐type granites characteristics. However, the post‐mineralization dioritic porphyrite displays strong depletions Sr, Ta, P, and Ti whereas Rb, Th, Ce, and Sm are enriched, enriched in LREE with weakly negative Eu anomalies. The metallogenic granite porphyry is significantly enriched in Au, As, Sb, W, Mo, and Bi, especially enriched in Au. The Lu‐Hf isotopic data indicate that the magma source comes from the partial melting of the Paleoproterozoic crust, the minor part from the mantle in the Early Cretaceous. Therefore, we propose that the granitoids formed in the subducted plate environment from the Middle Jurassic to the Early Cretaceous, the Late Jurassic I‐type granites (~153–146 Ma), The Shuangqishan Au deposit was formed in the stage from compression to extension, the Early Cretaceous granites (~129–114 Ma) mainly formed in the extensional environment and destroyed gold ore bodies. [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]

The controversial topic of genetic relationships of shallow magmatogenic ore deposits with associated complexes of small intrusive bodies or separate syn-ore bodies is discussed in this article. Materials of the field study by the authors of four epithermal gold deposits of the Amur region are used. These materials are supplemented by an analysis of published data on the conditions and geological settings of the localization of a number of other epithermal and shallow Cu-Mo-porphyry deposits in various regions of Russia and other countries. The active thermal participation signs of syn-ore stocks and sill in retraction to intrusions and initiation of near-intrusive convection of deep-seated fluids during ore formation at epithermal gold deposits of the Amur region (Pokrovskoe, Pioner, Zheltunak, Bamskoe, and Mnogovershinnoe) have been established and confirmed by model experiments. These signs and zoning of metal deposition are also established at epithermal and porphyry deposits in other regions of Russia (Ural, Transbaikalia, and Kamchatka) and in other countries. Favorable conditions for ore accumulations have been identified. These conditions are associated with shallow syn-ore small intrusions and magma chambers at 11 characteristic deposits, including large and unique ones (Pioner, Mnogovershinnoe, Bingham, and Klaimax). [ABSTRACT FROM AUTHOR]

Known to be triggered and controlled by tectonic systems, magmatism plays a significant role in the deposition and emplacement of hydrothermal mineral systems. It is, therefore, of paramount importance to recognize the tectonic processes that are genetically associated with hydrothermal mineral systems. This study seeks to address this research gap by recognizing the main tectonic processes that have controlled the distribution of porphyry copper (Cu) deposits in Dehaj Area on the Urmia-Dokhtar magmatic belt, central Iran. For this purpose, spatial associations of 31 known porphyry Copper deposits, faults, and fractures were evaluated by multiple numerical techniques including fry, fractal, (box-counting and radial-density methods), and distance-distribution analyses to investigate structural controls of the porphyry Copper mineralization. Results of the fry analysis revealed three mineralization trends, namely NS, NE, and NW, clearly following the existing fault systems in the area. Application of the fractal method demonstrated that structural controls on mineralization have operated on two different scales, regional and local scales. Distance-Distribution analysis was further used to spatially correlate known porphyry Copper deposits to fault traces, supplementing the results of fry and fractal analyses by quantitative measurements. Compiling the results of these three methods, it was shown that NW-trending faults have plausibly controlled the magmatism on a regional scale. On a local scale, however, NE- and N-trending faults have probably acted to control the channelling and emplacement of mineral-bearing fluids. [ABSTRACT FROM AUTHOR]

The Maricunga metallogenic belt, herein defined to encompass the region from 25° S to 28° S along the Cordillera Frontal of northern Chile, is known for hosting a series of gold-copper and lesser copper-molybdenum porphyries and gold-silver epithermal systems that are hosted in a segment of the late Oligocene-Miocene Andean calc-alkaline magmatic arc. Based on an up-to-date geochronological database, four episodes of magmatism and related hydrothermal deposits are proposed to characterize intensity and style of volcanism and hypabyssal intrusive rocks over time. The late Oligocene episode (26-21 Ma) is characterized by stratovolcanoes, dome complexes, pyroclastic sequences, and hypabyssal intrusives of andesitic to dacitic composition that host gold-rich porphyry systems such as Caspiche, Maricunga, and La Pepa. The early Miocene episode (21–17 Ma) has similar rock types but is volumetrically reduced, hosting epithermal and porphyry deposits like La Coipa and Caserones, respectively. A reinvigoration of volcanism occurred during the third stage between 17 and 11 Ma, giving rise to large volcanic complexes and intra-to extra-caldera ignimbritic deposits that host several gold-rich porphyry deposits such as Lobo-Marte, Luciano, and Cerro Casale; as well as epithermal deposits such as Fenix. Some of the 17 to 11 Ma and younger igneous rock belong to the high-K calc-alkaline series, showing a higher alkali content compared to previous periods. The last magmatic episode, from 11 to 5 Ma, coincides with the shallowing of the subduction angle and is characterized by an eastward migration of volcanism, and more heterogeneous rocks including trachytic compositions. During this period mineralization was emplaced at the Salares Norte epithermal deposit and El Volcan porphyry Au–Cu deposit. Porphyry and epithermal systems formed throughout the evolution of the Maricunga belt. Overprint of advanced argillic alteration on porphyry style alteration is widespread albeit commonly devoid of significant addition of epithermal Au–Ag mineralization. The Au-rich nature of the majority of the porphyry systems is attributed to the shallow crustal depths of emplacement compared to Cu- and Mo-rich porphyry systems. Conversely, high-sulfidation epithermal Au–Ag deposits such as La Coipa and Nueva Esperanza are not known to be telescoped on coeval porphyry gold deposits. The location of the mineralized centers was favored by crustal weaknesses expressed by intersection of oblique- and parallel-to arc structures, the former inherited from the construction of the continent before to the formation of the Andean range. The arc oblique structures also segment the Maricunga belt into domains with unique magmatic and hydrothermal styles. • This is an updated compilation of the distribution of magmatism and related mineralization within the Maricunga belt. • The belt is segmented by major cross-strike structural corridors which control the styles of mineralization for each segment. • Mineralization events that defined the Maricunga belt covered a more extensive area from original models. [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]

Arc basalts with high H 2 O content are expected to evolve into highly hydrated felsic melts saturated with aqueous fluids at lower crustal pressures, which are potentially important in providing sulfur (S) and metals for porphyry deposit formation. However, the role of such highly hydrated and fluid-saturated magmas in the transfer of S (and metals) remains rarely studied. To investigate the S dissolution capacity of highly hydrated felsic magmas saturated with fluids at the lower crustal conditions, this study performed experiments with dacite + 10 wt% FeS at H 2 O contents of 10, 15, and 20 wt%. All the experiments were performed in piston-cylinder apparatus at 1.0 GPa and 950 °C with f O 2 conditions imposed by the following solid-state buffers: cobalt-cobalt oxide (CCO), nickel-nickel oxide (NNO), rhenium-rhenium oxide (RRO), MnO-Mn 3 O 4 (MMO), and hematite-magnetite (HM), resulting in a f O 2 range of FMQ−1.5 to FMQ+3.3 log units (FMQ = fayalite + magnetite + quartz oxgen buffer). The experimental results show that the H 2 O content in the felsic melt, in addition to f O 2 and melt composition, has a strong effect on the concentration of S in the silicate melt at sulfide ± anhydrite saturation. At a given f O 2 , the S concentration in the melt increases with increasing H 2 O content (hydration), resulting in a S concentration of up to ∼8000 ppm in the highly hydrated dacitic melts at f O 2 ∼ FMQ+2. We found that high melt hydration at an intermediate f O 2 not only dramatically increases sulfide and anhydrite solubilities in the dacitic melts but also promotes the saturation of S-rich fluids. The S concentration in the fluid that corresponds to the highest measured S concentrations in the melt (∼8000 ppm) are ∼5 wt%. These results show that highly hydrated felsic magmas saturated with fluids have a high capacity for S dissolution. Therefore, injection of such fluid-saturated magmas from lower crustal to shallow magma reservoirs is a potential mechanism for the effective transport of S (and perhaps metals) to facilitate subsequent porphyry ore deposit formation. [ABSTRACT FROM AUTHOR]

Porphyry deposits host various trace elements in economic amounts, but the hydrothermal processes causing their fractionation and enrichment are still not fully understood, but vital to target the most prospective mineralisation. We present the first micro-analytical study on the trace element composition of pyrite from the Koloula Cu-Au porphyry in the young and thin (<25 km) Solomon Islands arc. A statistical evaluation of the trace element data of pyrite indicates that mineral inclusions obscure the chemical signature of the mineralisation processes. The filtered pyrite data, from which the inclusions were excluded, correlate with variations in temperature and salinity, as defined by fluid inclusions from several alteration zones. Trace element ratios in pyrite show systematic variations with fluid temperature and salinity (Co/Ni, Se/Te), phase separation (Co/Ni, Co/As) and mixing of magmatic fluids and meteoric waters (Se/Ge). The mineralisation in the potassic alteration zone was controlled by the formation of a hypersaline liquid (Co/As > 1, Co/Ni > 50) from a magma-derived fluid (Se/Ge ~ 100) at lithostatic pressure conditions and temperatures of up to 700 °C (Se/Te > 50). This was followed by a transition to hydrostatic pressure conditions due to open-fracture continuity towards the paleo-surface, marking the onset of boiling in the chlorite-sericite to sericitic alteration zone (Co/As < 1), where minor proportions of meteoric water were involved (Se/Ge < 100). The shallowest part of the mineralisation is controlled by lower temperature (<300 °C, Se/Te < 50) vapour-rich fluids (Co/As < 1) that condensed into meteoric waters in an epithermal transition zone (Co/Ni < 50, Se/Ge < 100). Trace element systematics in pyrite from progressive alteration zones therefore preserve the time-space evolution of porphyry (-epithermal) systems in young and thin oceanic island arcs. [ABSTRACT FROM AUTHOR]

Čukaru Peki is a recently discovered porphyry- high-sulfidation Cu-Au deposit located 5km south of the mining town of Bor in east Serbia. Three styles of mineralization are distinguished in the Čukaru Peki system: a high-sulfidation type with massive sulfides (named the Upper zone), a porphyry type (named the Lower zone) and a transition type (between porphyries and massive sulfides). This study investigates the concentration and distribution of trace elements in pyrite from these three mineralization zones of Čukaru Peki. The high-sulfidation pyrite contains elevated concentrations of V, Mn, Ni, Cu, As, Mo, Ag, Cd, In, Sn, Sb, Au, Hg, Tl, Pb and Bi, compared to pyrite from the porphyry zone. The porphyry zone pyrite contains elevated concentrations of Co and Se. The sample from the transition zone contains concentrations between the two other zones, with the exception of the relative enrichment of Co and Ag. This research also aims to separate different stages of ore deposition. The porphyry stage contains several types of veins: quartz A veins, quartz B veins, pyrite D veins, magnetite veins, purple anhydrite veins, sulfide veins and orange anhydrite veins. The high sulfidation stage also formed in several stages: pyrite1, pyrite-enargite veins, pyrite-covellite veins, pyrite2 veins and calcite-anhydrite veins. There are distinct differences between various vein generations found within each zone, notable examples are the enrichment of Se in quartz B veins pyrite and Cu in sulfide veins, compared to other veins from porphyry zone veins and the enrichment of several trace elements (Cu, Mo, Ag, Cd, In, Sn, Sb, Au, Hg, Tl, Pb and Bi) in pyrite from the Py-cov veins in comparison to the other high-sulfidation veins. The trace element data also indicates a change in fluid compositions; the earlier fluids responsible for the porphyry zone mineralization showing a slightly more magmatic fluid signature (higher Co/Sb and Se/As values) and the later high-sulfidation fluids bearing a more typical epithermal trace element signature, which indicates cooling and diluting of fluids. Some of the porphyry zone pyrite crystals (from B-type veins and Purple anhydrite-veins) contain elevated concentrations of elements attributed to the high-sulfidation zone (e.g. Cu, Ag, Cd, In, Sn, Pb and Bi), which suggests that these veins were affected by later high-sulfidation fluids. [ABSTRACT FROM AUTHOR]

The Huangshaping deposit is unique in southern Hunan Province, China, as it hosts economic reserves of both W–Mo and Pb–Zn mineralization, which are usually associated with granite and granodiorite porphyry in this area, respectively. This study reports results of in situ LA-MC-ICP-MS sulphur isotopic composition analyses conducted on sulphides from both W–Mo and Pb–Zn mineralization from the Huangshaping deposit with the aim of constraining ore genesis for this deposit. All samples from the proximal W–Mo mineralization have relatively uniform and high δ34S values (8.7 ‰ to 16.0 ‰), close to the range for carbonate sediments in this deposit (13.8 ‰ to 18.1 ‰). These patterns suggest that the granite porphyry in this deposit was the sulphur source for W–Mo mineralization, and that the assimilation of evaporite from the carbonate sediments led to the high δ34S values of the granite porphyry. Sulphides from the Pb–Zn mineralization have δ34S values (2.2 ‰ to 10.3 ‰) lower than those of the W–Mo mineralization, and generally increase in this paragenetic order, with the lowest δ34S values being similar to those of the basement (3.8 ‰ to 7.7 ‰). These patterns indicate that the original sulphur for the Pb–Zn mineralization was most likely derived from the basement, with input of sulphur from the carbonate sediments increasing during the evolution of ore-forming fluids. On the basis of the measured sulphur isotopic compositions, it is suggested that the ore-forming materials for the W–Mo mineralization were derived from the granite porphyry, whereas ore-forming materials extracted from the basement dominated the Pb–Zn mineralization. [ABSTRACT FROM AUTHOR]

The Zhashui-Shanyang ore cluster area is one of the most important gold polymetallic ones in northwestern China. The Qinglingou gold deposit is a newly discovered small-scale deposit in the Zhashui-Shanyang area. Gold mineralization closely related to acid intrusive rocks has been found for the first time in this area. In this paper, the geochronology, whole-rock geochemistry, and isotope signature of the granite porphyries in the deposit are studied. They are characterized by variable medium SiO2 (67.22–71.72 wt.%), high K2O + Na2O contents (6.54–10.34 wt.%), and variable Al2O3 (14.47–15.10 wt.%) values. The A/CNK ratios range from 0.90 to 1.23, and the A/NK ratios vary from 1.14 to 1.48. These rocks also contain biotite and amphiboles and are similar to peraluminous and high-K calc-alkaline I-type granites. The Qinglingou granite porphyries show relative enrichment of Rb, Th, and K, and depletion of Nb, Ta, P, Ti, and other high field strength elements. These porphyries are enriched in light rare earth elements relative to heavy rare earth elements with weak negative Eu anomalies (δEu = 0.63–0.89), which is interpreted to be the best age of crystallization of the Qinglingou porphyries. LA–ICPMS zircon U–Pb dating yields an age of 211 ± 1.2 Ma (n = 16, MSWD = 0.39). The close spatial relationship between the ore bodies and granite porphyry dikes indicates that this age may represent the metallogenic age in this area. The zircons have 176Hf/177Hf ratios ranging from 0.282625 to 0.282702, the εHf(t) values are near 0 and the two-stage zircon Hf model ages range from 1121 to 1296 Ma. These data indicate that the Qinglingou granite porphyries were derived from the interplay between mantle- and crustal-derived magmas. We therefore propose that there is potential gold in carbonate rocks at the periphery of porphyry-skarn copper-molybdenum deposits. [ABSTRACT FROM AUTHOR]

The paper reviews and summarizes data on the physicochemical parameters and chemical features of mineralizing fluids at porphyry deposits of the Cu–Mo–Au system. The calculated average values and ranges of parameters of the fluids in mineral-hosted fluid inclusions at porphyry deposits are as follows: temperature 90–957 °C, average 388 °C; salinity 0.1–88.0 wt % equiv. NaCl, average 29.4 wt % equiv. NaCl; and density 0.38–1.85 g/cm3, average 0.93 g/cm3. The highest average temperature and the highest maximum homogenization temperatures of the fluids were detected at deposits of the Cu (Au) type, with both values systematically decreasing with the transition to the Cu, Mo (Au), and then to Mo and Au types of porphyry deposits. The situations with the average and maximum salinity values of the fluids and their density are analogous. The data in the literature on the concentrations of some elements are still insufficient to reliably characterize variations in these concentrations at all of the discussed types of porphyry deposits. The highest Cu and Fe concentrations were found in the highest temperature fluids at deposits of the Cu (Au) type. The maximum Mo concentrations were detected in fluids at porphyry Mo deposits, and the highest Ag concentrations occurred at porphyry Au deposits. The chemical composition of the mineralizing fluids is, thus, strongly correlated with the types of the porphyry deposits. The hypothesis is discussed: the geochemical specifics of mineralizing fluids at various types of porphyry deposits of the Cu–Mo–Au system are related to the depths at which fluid separated from the magmatic melt. A scenario is proposed for the separation of mineralizing fluids from granite melt at various depths for fluids that form different types of porphyry deposits. [ABSTRACT FROM AUTHOR]

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South China can be divided into four metallogenic belts: The Middle-Lower Yangtze Metallogenic Belt (MLYB), Qinzhou-Hangzhou Metallogenic Belt (QHMB), Nanling Metallogenic Belt (NLMB), and Wuyi Metallogenic Belt (WYMB). The major mineralization in the four metallogenic belts is granite-related Cu–Au–Mo and porphyrite Fe-apatite, porphyry Cu (Au), and epithermal Pb–Zn–Ag, hydrothermal Cu–Au–Pb–Zn–Ag, and granite-related skarn-type and quartz-veins W–Sn, respectively. Low-temperature thermochronology, including fission-track and U-Th/He dating, has been widely used to constrain tectonic thermal evolution and ore deposits preservation. Understanding fission-track annealing and He diffusion kinetics in accessory minerals, such as zircon and apatite, is essential for dating and applications. In this study, previous zircon fission-track (ZFT) and apatite fission-track (AFT) ages in South China were collected. The result shows that the ZFT ages are mainly concentrated at 140–90 Ma, and the AFT ages are mainly distributed at 70–40 Ma. The age distribution and inversion temperature–time paths reveal heterogeneous exhumation histories in South China. The MLYB experienced Late Cretaceous-Cenozoic extremely slow exhumation after rapid cooling in the Early Cretaceous. The northern QHMB (i.e. from southern Anhui province to the Hangzhou Bay) had a relatively faster rate of uplifting and denudation than the southern QHMB in the Cretaceous. Subsequently, the northern QHMB rapidly exhumed, while the continuously slow exhumation operated the southern QHMB in the Cenozoic. The southern NLMB had a more rapid cooling rate than the northern NLMB during the Cretaceous time, and the whole NLMB experienced rapid cooling in the Cenozoic, except that the southern Hunan province had the most rapid cooling rate. The WYMB possibly had experienced slow exhumation since the Late Cretaceous. The exhumation thickness of the four metallogenic belts since 90 Ma is approximately calculated as follows: the MLYB ≤ 3.5 km, the northern QHMB concentrated at 3.5–5.5 km, and the southern QHMB usually less than 3.5 km, the NLMB 4.5–6.5 km and the WYMB < 3.5 km. The exhumation thickness of the NLMB is corresponding to the occurrence of the world-class W deposits, which were emplaced into a deeper depth of 1.5–8 km. As such, we infer that the uplifting and denudation processes of the four metallogenic belts have also played an important role in dominated ore deposits. [ABSTRACT FROM AUTHOR]

The Tonggou deposit is a porphyry Cu and vein-type Cu-Zn mineralization system located in the Bogda Orogenic Belt, north of Eastern Tianshan. Systematic fluid inclusion analyses were performed on granular quartz from the magnetite–quartz stage and pyrite–chalcopyrite–quartz stage from the porphyry Cu mineralization. During the early stage of porphyry Cu mineralization, the ore-forming fluids were at high temperatures (450–501 °C) and high salinity (51.2–55.2 wt.% NaCl equiv.) H2O-NaCl hydrothermal fluids with fluid boiling. These fluids evolved to high temperature (412–450 °C) and intermediate to low salinity (8.3–14.2 wt.% NaCl equiv.) H2O-NaCl hydrothermal fluids during the pyrite–chalcopyrite–quartz stage. In addition, magnetite from the Tonggou deposit was studied as a marker for the ore-forming process evolution of porphyry and vein-type mineralization. Sampled magnetite can be divided into MagI (allotriomorphic magnetite from altered granodiorite), MagII (magnetite from altered granodiorite found in veinlets or as granular aggregates), MagIII (from the magnetite–quartz stage of porphyry mineralization), and MagIV (from the polymetallic sulfide–epidote–quartz stage of vein-type mineralization). Magnetite LA-ICP-MS data indicate a hydrothermal origin. The contents of Ti, Si, Al, and Ta are controlled by temperature, and these elements gradually decrease from MagI to MagIV. Moreover, fO2 has considerable influence on the substitution of Sn, V, and Mn in magnetite, and the contents of these elements generally decrease from MagI to MagIII—increasing only in MagIV. Indeed, high fO2 in the polymetallic sulfide–epidote–quartz stage (MagIV) of vein-type mineralization is shown by the presence of a replacement texture in ilmenite grains within hydrothermal magnetite. On the other hand, magnetite samples from the Tonggou deposit have relatively low Ti + V contents compared to other porphyry Cu deposits—plotting in the skarn field of the (Ti + V) vs. (Ca + Al + Mn) diagram—and shows negative correlations in the (Ti + V) vs. Sn diagram. These data indicate that the porphyry Cu mineralization at Tonggou formed at relatively lower fO2 conditions than the Tonggou vein-type mineralization and other typical porphyry Cu deposits. Finally, porphyry and vein-type mineralization at Tonggou are both sourced from the porphyry system, as a result of ore-forming fluid transfer to a different location. [ABSTRACT FROM AUTHOR]

[Display omitted] • The Qi189 porphyry gold deposit has mantle component up to 37%. • Gold enrichment is controlled by changes in the pH, log f O 2 , log f S 2 , and log f Te 2. • Precipitation of native Au and Au-bearing telluride is significant for Au enrichment. The Qiyugou gold orefield is situated in the Eastern Qinling. It is a magmatic hydrothermal system, which includes cryptoexplosive breccia-type, vein-type, and porphyry gold deposits. However, the gold sources and physical–chemical conditions of precipitation of the newly discovered porphyry gold deposit, the Qi189, have not yet been well studied. It also hinders the comprehensive understanding of magmatic–hydrothermal gold systems in the Qiyugou gold orefield. Thus, detailed field and microscopic observations, C–O–He–Ar isotopic analysis, in situ major/trace element analysis, and thermodynamic studies on the Qi189 porphyry gold deposit have been carried out in this study. This deposit has three hydrothermal stages: the (I) early quartz–K-feldspar–molybdenite–magnetite stage, (II) middle quartz–sericite–pyrite–Te–Bi-mineral stage, as well as (III) late calcite–quartz stage. The carbon and He–Ar isotopic compositions suggest deep-seated sources of ore-forming fluids with mantle component proportions of up to 37 %. Oxygen isotopic compositions indicate the gradual involvement of more meteoric water in ore-forming fluids during stages I–III. The meteoric water input and reduction in temperature and pressure in the early stage II increased oxygen fugacity and decreased the pH values of ore-forming fluids. Then, in hematite and sulfides formation during late stage II, the oxygen and sulfur fugacities of ore-forming fluids gradually decreased. Precipitation of native gold and Au-bearing telluride grains with quartz-sericite alteration in stage II is significant for Au enrichment, which occurred under acidic (pH = 3.64–5.71), low-log f O 2 (<-34.86), low-log f S 2 (−13.07 to −11.13) and low-log f Te 2 (−15.55 to −10.32) conditions. Therefore, abundant mantle components and changes in the pH, log f O 2 , log f S 2 , and log f Te 2 of the ore-forming fluids play important roles in gold enrichment. Combined with previous studies, this work also provides some new evidence for identifying a magmatic-hydrothermal gold system in this district, including similar sulfide trace elements, δ13C V-PDB compositions, and changes in log f O 2 and log f S 2 of various types of gold deposits in a gold orefield. [ABSTRACT FROM AUTHOR]

[Display omitted] • Unidirectional solidification texture can chronicle the magmatic-hydrothermal evolution. • Multi-generational quartz distinguished by CL textures manifests the overall evolutionary history at Lailisigaoer. • Aluminum, Ti, Na and K can directly or indirectly signify variations in CL intensity of quartz. • Decompression, cooling, and the CO 2 concentration in hydrothermal fluid trigger Mo precipitation at 3.4–3.6 km. The Lailisigaoer deposit is a typical porphyry Mo deposit located in the late Paleozoic Boluokenu metallogenic belt of Western Tianshan, NW China. This study aims to understand molybdenum mineralization and the dynamics of magmatic-hydrothermal fluid within the porphyry system, focusing on fluid inclusion, cathodoluminescence textures, and trace elemental composition in various generations of quartz. Six vein types in the Lailisigaoer deposit are classified as comb quartz veins with unidirectional solidification texture (UST, Q I), actinolite/biotite ± quartz veinlets (M-type, Q II), quartz-chalcopyrite vein (A-type, Q III), quartz-molybdenite vein (B-type, Q IV), quartz-pyrite vein (D-type, Q V) and quartz-carbonate vein (E-type, Q VI). Micro thermometry data indicate decreasing homogenization temperatures in primary fluid inclusions from UST to E-type veins. The magmatic-hydrothermal fluids associated with UST and M-, A-, B-, D-, E-type veins underwent a transition from high temperature (342–495℃), high-pressure (∼1.25 kb), and variable salinity (6.7–41.1 wt%NaCl) in the H 2 O-CO 2 -NaCl system to low-temperature (142–238℃), low-pressure (∼0.25 kb), and low-salinity (1.6–5.1 wt%NaCl) in the H 2 O-NaCl system. This evolution is reflected in the proportion of quartz with oscillatory zones decreasing and irregular quartz increasing, indicating a shift from turbulent to stable fluid conditions. Furthermore, a gradual reduction in Ti concentration (from 79 ppm in UST to 1.4 ppm in E-type quartz) suggests a decrease in fluid temperature during the magmatic-hydrothermal evolution. Mineralization primarily occurs in A- and B-type veins, with molybdenum precipitation attributed to fluid immiscibility in a medium–high temperature (240–368 ℃) and high pressure (∼0.95 kb) environment. The A-type veins (mean 31 ppm in Ti concentrations) consist of equigranular (dark-core) (Q III-1) and patchy inhomogeneous CL-gray quartz (Q III-2). The B-type veins (mean 24 ppm in Ti concentrations) are characterized by equigranular (bright-core) inhomogeneous quartz (Q IV-1) with growth zones that are cemented by later mosaic homogeneous CL-gray quartz (Q IV-2). Based on the quartz-Ti thermometer, the mineralized veins (A- and B-type) were confined to be formed at depths of 2.8–3.6 km, with molybdenum mineralization occurring at 3.4–3.6 km. Molybdenum mineralization initiates during the Q IV-1 crystallization period in magmatic-hydrothermal fluids and terminates in the Q V-2 generation. [ABSTRACT FROM AUTHOR]

[Display omitted] • Molybdenite Re-Os and sericite 40Ar-39Ar dating results show that the Xinan deposit is formed at 109 ∼ 108 Ma. • Fluid cooling, oxygen fugacity reduction, and CO 2 escape control Cu-Mo mineralization of the Xinan deposit. • Possible porphyry mineralization center at depth is inferred by fluid inclusion microthermometry. The Xinan deposit, a newly discovered porphyry Cu-Mo deposit in the Zijinshan orefield, Fujian Province, exhibits distinct alteration and porphyry mineralization stages, including the potassic, propylitic, and phyllic alteration stages. The phyllic stage is further divided into molybdenite, chalcopyrite, and pyrite sub-stages. Molybdenite Re-Os model age (108.3 ± 1.1 Ma) and concomitant sericite 40Ar/39Ar plateau age (109.0 ± 6.0 Ma) indicate that the Xinan Cu-Mo deposit was formed at 109 ∼ 108 Ma. Four types of fluid inclusions have been identified at the Xinan deposit, including vapor-rich, liquid-rich, and opaque daughter mineral-bearing subtypes with minor transparent daughter mineral-bearing subtypes. Fluid inclusion microthermometry measurements reveal that the potassic alteration stage exhibits homogenization temperatures of 375–475 °C and salinities range of 4–20 wt% NaCl eqv., suggesting slight fluid boiling. Chlorite geothermometer suggests temperatures of the propylitic alteration stage range from 261 to 336 °C, averaging at 303 °C. The molybdenite, chalcopyrite, and pyrite sub-stages have homogenization temperatures of 325–400 °C, 325–350 °C, and 300–350 °C, respectively, with corresponding salinities of 2–10 wt% NaCl eqv., 4–8 wt% NaCl eqv., and 2–4 wt% NaCl eqv.. The Laser Raman spectroscopy results show that the fluid inclusions in the Xinan deposit consist of H 2 O with minor CO 2 , hematite, chalcopyrite, and halite. The evolution of the ore-forming fluids in the Xinan porphyry Cu-Mo deposit is characterized by a transition from high-temperature, low- to moderate-salinity, oxidized, and CO 2 -bearing conditions during the potassic alteration stage, to moderate- to high-temperature and low-salinity conditions during the propylitic alteration stage. The subsequent phyllic alteration stage, which overprints on the potassic and partial propylitic alteration stages, is marked by moderate- to high-temperature, low-salinity, and low-oxygen fugacity environments. The primary mechanisms driving mineralization in the Xinan porphyry Cu-Mo deposit are thus identified as the reduction in temperature and oxygen fugacity, coupled with CO 2 escape. In contrast to the Luoboling-Jintonghu porphyry Cu-Mo deposit, the ore-forming fluid of the Xinan deposit is characterized by lower temperatures, salinity, and CO 2 contents, and reduced fluid boiling. This suggests a relatively subdued porphyry-type mineralization. The lack of a distinct potassic alteration zone in the Xinan Cu-Mo deposit suggests the potential existence of a deeper, higher temperature and salinity porphyry mineralization center beneath this deposit. [ABSTRACT FROM AUTHOR]

[Display omitted] • Based on the EPMA analyses, sulfosalts were identified at the Chodarchay deposit. • The chalcopyrite and sphalerite host solid-solution Ag, and the chalcopyrite hosts Ag-sulfosalt. • The sphalerite hosts nano-Au. The Au-Ag exists in the neyite, emplectite and gustavite. • The sphalerite precipitated from 220 to 280 °C, Bi assemblages at > 350 °C. • The supergene enrichment of Ag and Au depends on the presence of Mn. The Chodarchay overprinting epithermal on porphyry mineralization occurs in the Tarom-Hashtjin subzone of the Alborz magmatic arc in northwestern Iran. Rock units include intrusions (phases I and II) and volcano-volcaniclastic rocks. The alteration types consist of potassic, phyllic, argillic, and propylitic. The porphyry type is mostly accompanied by potassic alteration. The Chodarchay Fault implies two extensional and compressional mechanisms. The porphyry type is associated with the extensional and the epithermal type with the compressional stage of the fault. Mineralization occurred mainly inside the Eocene volcanic and volcano-sedimentary rocks; some ores are associated with the Late Eocene quartz monzonite. The mineralization is divided into three zones from depth to surface: 1) Hypogene sulfide zone (deep); 2) Enriched supergene sulfide zone (near-surface); 3) Oxidized and leached zone (surface). The major sulfide minerals consist of chalcopyrite, pyrite, sphalerite, and galena. Based on the results of the new analyses, chalcopyrite hosts Ag as a solid-solution and contains Ag-rich Bi-sulfosalt micro-inclusions. Non-constant Cd/Zn ratio in the chalcopyrite can indicate varying physiochemical conditions during its crystallization. Low As contents in the pyrite caused relatively clean pyrite with very few elements. The Ni concentrations in the pyrite imply that it was sourced from mantle mafic–ultramafic rocks. Sphalerite is the only Au-host mineral among the sulfide minerals as a nano-mineral phase. Solid-solution Ag exists in the sphalerite. The sphalerite Fe/Zn ratios show that it was precipitated between 220 and 280 °C. Silver and Bi have the highest measured concentrations among all analyzed elements in the galena, mainly partitioning within the galena, but Hg and Cd are abundant in the sphalerite. Bornite is one of the major carriers of Ag and Bi. Silver and Bi exhibit considerable variations in the Cu-(Fe) sulfides. A new occurrence of sulfosalt minerals was identified at Chodarchay (N = 14). The discovered Bi-sulfosalts include cuprobismuthite group minerals (cuprobismuthite, hodrushite, and paderaite), aikinite-bismuthinite series (aikinite and friedrichite), emplectite, makovickyite, galenobismutite, gustavite, heyrovskyite, neyite, cupropavanite; and As-Sb-bearing Cu sulfosalts (watanabeite and colusite). This number of sulfosalts had not previously been reported from any of the Tarom or Alborz deposits or mines. The Au-Ag occurrence was reported from the neyite, emplectite, and gustavite. The Ag-rich minerals crystallize from fractionated fluids that cooled during rising. Silver-carrier sulfosalts may have been exsolution from pre-existing Ag-bearing chalcopyrite in the cooling system. Most of the Ag-bearing sulfosalt minerals formed at the margins and fractures of the chalcopyrite, indicating that the cooling started from these points. Thus, Ag at Chodarchay is hosted inside Cu-(Fe) sulfides, the significant part of them being chalcopyrite and Ag-rich sulfosalt micro-inclusions inside the chalcopyrite. The fluid temperature for the Ag and chalcopyrite precipitation is from 200 to 350 °C. Bismuth assemblages precipitated at > 350 °C. The cuprobismuthite group crystallizes at temperatures > 300 °C. The supergene process and rare secondary enrichment of Ag and Au took place in the oxidation zone; this enrichment is dependent on the presence of manganese. Based on the fire-assay results, the concentration of gold is greater at shallower depths. [ABSTRACT FROM AUTHOR]

The study area is located in the southeastern Biga Peninsula. As result of field, drilling and laboratory studies, diorite porphyry intruded to Lower Miocene and older units and contained Au, Pb, Zn and Cu anomalies, has been determined. Intersected potassic, propylitic, phyllic and argillic alteration zones were developed in the pluton and host rock. Veins-veinlets developed in the pluton and host rock, contain native gold, silver, pyrite, chalcopyrite, sphalerite and galena. They are composed of undulated quartz in the deeper levels, and massive quartz, calcite/dolomite and barite in the middle and upper levels. According to the fluid inclusion data from sphalerite, quartz and barite, temperature of ore-bearing fluids are in three groups (argillic:150-220°C, phyllic:250-350°C, potassic:>400°C). Fluid inclusions, including solid phases such as hematite, chalcopyrite and salt as well as liquid and gas phases, indicate that Çatalçam Au-Cu mineralization is intrusion-related system. Fluid inclusion data display temperature and salinity of the ore-bearing fluids in the early stage (porphyry) are high, whereas relatively lower in the late stage (epithermal). In conclusion, Çatalçam mineralization was developed in two different phases as porphyry Au-Cu and epithermal Zn-Pb-Cu-Au, which is the first porphyry gold deposit related to Miocene magmatic-hydrothermal system in the Biga porphyry belt. [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]

An indication of high‐sulfidation epithermal–porphyry transition was observed in the Kumbokarno prospect, East Java, Indonesia. The prospect is composed of two Middle Miocene intrusions with tonalitic and dioritic compositions. Tonalite, the main host‐rock was subjected to argillic, advanced argillic, and vuggy quartz alteration, whereas the juxtaposing diorite was subjected to peripheral propylitic alteration. Three types of vein exist in the research area, which are massive quartz, comb quartz, and stockwork vein. In addition, supergene alteration represented by goethite and hematite pervasively superimposed both the hydrothermal alteration and mineralization. Fluid inclusion petrography and microthermometry analysis on three types of quartz veins distinguished primary fluid inclusions into two groups, that is, V30 group composed of vapor (30 vol%)–liquid (70 vol%), and the second group V30H group composed of vapor (30 vol%)–halite (30 vol%)–liquid (40 vol%). The homogenization temperatures of both the groups show a similar range of ca. 350–480°C, but the V30H group has significantly higher salinity (35–50 wt% NaCl eq.) compared to the V30 group (10–20 wt% NaCl eq.). In terms of the vein types, the massive quartz vein has the highest homogenization temperatures, followed by the comb quartz vein and lastly the stockwork veins. The presence of alunite and its sulfur isotope compositions, δ34S = 19.6 (σ = 2.1‰), indicate acidic pH and presence of SO42− in the hydrothermal fluids. The prospect is an intrusion‐centered magmatic‐hydrothermal system reflecting the porphyry‐epithermal transition. The fluid inclusions with high homogenization temperatures up to 480°C and high salinity up to 50 wt% NaCl eq. also support the transition of porphyry to high‐sulfidation epithermal mineralization. The presence of two different types of primary fluid inclusions suggests that boiling process occurred and separated the original magmatic fluid into the liquid and vapor phases. More, this fluid underwent dilution and mixing with meteoric waters. The migration of both the fluids were likely unrelated to the formation of the advanced argillic–argillic alteration halo because the quartz veins cut across this alteration. The prospect was later subjected to intensive weathering process that altered most of the sulfides into iron oxides and hydroxides. Small amounts of copper and minor gold were detected, especially in the iron oxides and hydroxides ones with colloform and bladed textures. The Kumbokarno prospect evidences the potential for high‐sulfidation to porphyry deposits at the Southern Mountain Arc, Indonesia. [ABSTRACT FROM AUTHOR]

Airborne magnetic and radiometric data of parts of Zamfara, North West Nigeria, were analysed to delineate the structural complexity, emplacement of porphyry intrusives and hydrothermal alteration zones with a view to deducing optimum areas of mineralisation. These mineral indicators were achieved with the Centre for Exploration Targeting (CET) grid, CET porphyry analysis, and radiometric ratio maps. The result indicated that the structures within the study area trend in the NE–SW, WNW–ESE, ENE–WSW, NW–SE and E–W directions. Areas with high structural complexity have a high occurrence of porphyry features indicating a strong probability for further ore deposition. The porphyry features and hydrothermally altered zones from the K/eTh ratio map showed more structural relationships that aided the migration of hydrothermal fluids that react with rock formation for subsequent alteration. Mineral indicators from the various methods were integrated to proffer promising areas of mineralisation within the study area. [ABSTRACT FROM AUTHOR]

Ground magnetic surveys conducted in Suyoc, Mankayan, Benguet led to the delineation of features related to epithermal and porphyry copper targets in the area. High reduced to equator (RTE) anomalies are observed in areas with epithermal mineralization. The high RTE anomalies are attributed to hydrothermally altered rock with quartz veins. The previously recognized porphyry copper prospect in Palasaan (Mohong Hill) is characterized by low RTE anomaly surrounded by a high RTE anomaly. One explanation for this signature is the possible presence of a magnetic core and the destruction or absence of magnetite in the alteration haloes at the periphery of a porphyry prospect. Areas such as Mangga and Liten exhibit the same magnetic signatures. This distinct magnetic pattern coupled with observed alteration and mineralization signatures led to the interpretation of prospective blind porphyry deposits in these localities. Results of the study reveal the applicability of ground magnetic data in characterizing and extracting a potential area of mineralized zones at a regional scale. [ABSTRACT FROM AUTHOR]

Magmatic-hydrothermal gold–copper deposits in post-subduction settings represent essential targets for mineral exploration, but controls on their formation remain controversial. The early Cretaceous lode Au districts that formed during lithosphere destruction of the North China Craton provide an ideal opportunity to better understand the key tectono-magmatic factors responsible for the genesis of Au-rich deposits in post-subduction settings. Here, we present a LA-ICP-MS study of silicate melt inclusions and sulfide inclusions from ore-related mafic to intermediate rocks in the central Taihangshan Au district in the interior of the North China Craton to constrain the content and evolution of magmatic ore metals ± volatiles. The results, combined with numerical modeling, suggest that the ore-related magmas contained only a few ng/g Au, which is similar to the Au content of non-mineralization-related mafic to intermediate magmas worldwide. The low Au content of the lode Au-related magmas suggest that large volumes of magmas had to accumulate in the middle to lower crust through trans-lithospheric fault systems to produce the lode Au deposits. It is further suggested that the lode Au-related magmas were alkali-rich, hydrous, oxidized and relatively rich in sulfur and chlorine (mafic melt inclusions contain 0.14‒0.24 wt% S and 0.1‒0.2 wt% Cl). These properties are considered critical for the generation of auriferous ore fluids. By comparing the tectono-magmatic setting of the giant Jiaodong Au province (~ 4000 t Au) with the central Taihangshan district (~ 150 t Au), we propose that the much larger total Au tonnage of the Jiaodong district results from the accumulation of a much larger volume of ore-forming magmas at deep crustal levels, induced by a stronger degree of lithosphere modification. In addition, given that the composition of lode Au-related magmas is similar to that of porphyry Cu–Au-related magmas, the lack of giant, early Cretaceous porphyry Cu–Au deposits in the North China Craton suggests that strong extensional settings favor the formation of lode Au deposits instead of porphyry Cu–Au deposits. The present study, therefore, has general implications for the genesis of Au-rich deposits in strongly extensional settings. [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]