A magmatic source of hydrothermal sulfur for the Prominent Hill deposit and associated prospects in the Olympic iron oxide copper-gold (IOCG) province of South Australia

The Prominent Hill deposit is a world-class iron oxide copper–gold (IOCG) deposit in South Australia, characterized by a high Cu/S ratio of the dominant Cu-(Fe) sulfides hosted by hematite breccias. It contains a total resource of 278 Mt of ore at 0.98% Cu and 0.75 g/t Au. Prominent Hill is one of several IOCG deposits and numerous prospects in the Olympic IOCG province that are temporally associated with the 1603–1575 Ma Gawler Range Volcanics, a large igneous province including co-magmatic granitoid intrusions of the Hiltaba Suite. Globally, IOCG deposits share many similar features in terms of their geological environment and mineral association. However, it is not yet clear whether sulfur and copper originate from the same source rocks and which hydrothermal redox processes created the characteristic iron oxide enrichment. Highly variable sulfur isotope compositions of sulfides and sulfates in IOCG deposits have previously been interpreted in terms of diverse sulfur sources that may include contributions from magmatic, sedimentary, seawater or evaporitic sulfur. In order to test these alternatives, we performed a detailed sulfur isotope study of Cu-(Fe) sulfides from Prominent Hill and IOCG prospects nearby. The Prominent Hill deposit shows a wide range in δ³⁴S_V-CDT between − 33.5‰ and 29.9‰ for Cu-(Fe) sulfides, and a narrower range of 4.3‰ to 15.8‰ for barite. Iron sulfides (pyrite, pyrrhotite) show a narrow range in sulfur isotope composition, whereas Cu-bearing sulfides show a much wider range, and more negative δ³⁴S_V-CDT values on average. We propose a two-stage sulfide mineralization model for the IOCG system in the Prominent Hill area, in which all hydrothermal sulfur is ultimately derived from a magmatic source that had a composition of 4.4 ± 2‰. The diversity in sulfur isotope composition can be produced by different fluid evolution pathways along reducing or oxidizing trajectories. A reduced sulfur evolution pathway is responsible for stage I mineralization, when intrusion-derived magmatic-hydrothermal fluids produced early pyrite and minor chalcopyrite at Prominent Hill, and iron ± copper sulfides in regional magnetite skarns and in some pervasively altered volcanic rocks of the Gawler Range Volcanics. Shallow-venting magmatic-hydrothermal fluids and subaerial volcanic gases that became completely oxidized by reaction with atmospheric oxygen produced sulfate and sulfuric acid with a sulfur isotope composition equal to their magmatic source. This highly oxidized ore fluid probably consisted dominantly of water from the hydrosphere, but contained magmatic solute components, notably sulfate, acidity and Cu. Sulfate reduction produced hydrothermal Cu sulfides with a wide range in sulfur isotope compositions from very negative to moderately positive values. Partial reaction of the Cu-rich stage II fluid with earlier stage I sulfides resulted in mixing of sulfur derived from sulfate reduction and from sulfides deposited during stage I. Modeling of the sulfur isotope fractionation processes in response to reducing and oxidizing pathways demonstrates that the entire spectrum of sulfur isotope data from stage I and stage II mineralization can be explained with a single, ultimately magmatic sulfur source. Such a magmatic sulfur source is also adequate to explain the complete spectrum of sulfur isotope data of other IOCG prospects and deposits in the Olympic province, including Olympic Dam. The results of our study challenge the conventional model that suggests the requirement of multiple and compositionally diverse sulfur sources in hematite-breccia hosted IOCG style mineralization.     

Paleogene magmatism and gold metallogeny of the Jinping terrane in the Ailaoshan ore belt,Sanjiang Tethyan Orogen (SW China): Geology,deposit type and tectonic setting

The Jinping terrane is situated in the southern segment of the Ailaoshan ore belt, Sanjiang Tethyan Orogen (SW China). The Paleogene intrusions in Jinping consist of syenite porphyry, fine-grained syenite and biotite granite stocks/dikes, and contain relatively low TiO₂ (0.21–0.38 wt%), P₂O₅ (0.01–0.35 wt%), and high Na₂O (2.00–4.62 wt%) and K₂O (4.48–7.06 wt%), belonging to high-K alkaline series. Paleogene gold mineralization in Jinping comprises four genetic types, i.e., orogenic, alkali-rich intrusion-related, porphyry and supergene laterite. The NW–NNW-trending faults and their subsidiaries are the major ore-controlling structures. The orogenic Au mineralization, dominated by polymetallic sulfide-quartz veins, occurs in the diorite and minor in Silurian-Devonian sedimentary rocks. It contains a CO₂-rich mesothermal fluid system generated from the mixing of mantle-derived fluids with crustal-derived metamorphic fluids, and the ore-forming materials were upper crustal- or orogenic-derived. The alkali-rich intrusion-related Au mineralization is hosted in the Ordovician-Silurian sedimentary rocks and minor in the Paleogene alkaline intrusions, and the Au orebodies occur predominantly in the alteration halos. It contains a CO₂-bearing, largely metamorphic-sourced mesothermal fluid system, and the ore-forming materials were derived from the ore-hosting rocks and minor from the alkali-rich intrusions. The porphyry Cu-Mo-Au mineralization occurs in the granite/syenite porphyries and/or along their contact skarn, with the mineralizing fluids being magmatic-hydrothermal in origin. The former two hypogene Au mineralization types in Jinping were mainly formed in the late Eocene (ca. 34–33 Ma) and slightly after the porphyry Cu-Mo-Au mineralization (ca. 35–34 Ma), which is coeval with the regional Himalayan orogenic event. Subsequent weathering produced the laterite Au mineralization above or near the hypogene Au orebodies.     

The Archean BIF-hosted Cuiabá Gold deposit,Quadrilátero Ferrífero,Minas Gerais,Brazil

The Cuiabá Gold Deposit is located in the northern part of the Quadrilátero Ferrífero, Minas Gerais State, Brazil. The region constitutes an Archean granite–greenstone terrane composed of a basement complex (ca. 3.2 Ga), the Rio das Velhas Supergroup greenstone sequence, and related granitoids (3.0–2.7 Ga), which are overlain by the Proterozoic supracrustal sequences of the Minas (< 2.6–2.1  Ga) and Espinhaço (1.7 Ga) supergroups.The stratigraphy of the Cuiabá area is part of the Nova Lima Group, which forms the lower part of the Rio das Velhas Supergroup. The lithological succession of the mine area comprises, from bottom to top, lower mafic metavolcanics intercalated with carbonaceous metasedimentary rocks, the gold-bearing Cuiabá-Banded Iron Formation (BIF), upper mafic metavolcanics and volcanoclastics and metasedimentary rocks. The metamorphism reached the greenschist facies. Tectonic structures of the deposit area are genetically related to deformation phases D₁, D₂, D₃, which took place under crustal compression representing one progressive deformational event (E_n).The bulk of the economic-grade gold mineralization is related to six main ore shoots, contained within the Cuiabá BIF horizon, which range in thickness between 1 and 6 m. The BIF-hosted gold orebodies (> 4 ppm Au) represent sulfide-rich segments of the Cuiabá BIF, which grade laterally into non-economic mineralized or barren iron formation. Transitions from sulfide-rich to sulfide-poor BIF are indicated by decreasing gold grades from over 60 ppm to values below the fire assay detection limit in sulfide-poor portions. The deposit is “gold-only”, and shows a characteristic association of Au with Ag, As, Sb and low base-metal contents. The gold is fine grained (up to 60 μm), and is generally associated with sulfide layers, occurring as inclusions, in fractures or along grain boundaries of pyrite, the predominant sulfide mineral (> 90 vol.%). Gold is characterized by an average fineness of 0.840 and a large range of fineness (0.759 to 0.941).The country rocks to the mineralized BIF show strong sericite, carbonate and chlorite alteration, typical of greenschist facies metamorphic conditions. Textures observed on microscopic to mine scales indicate that the mineralized Cuiabá BIF is the result of sulfidation involving pervasive replacement of Fe-carbonates (siderite–ankerite) by Fe-sulfides. Gold mineralization at Cuiabá shows various features reported for Archean gold–lode deposits including the: (1) association of gold mineralization with Fe-rich host rocks; (2) strong structural control of the gold orebodies, showing remarkable down-plunge continuity (> 3 km) relative to strike length and width (up to 20 m); (3) epigenetic nature of the mineralization, with sulfidation as the major wall–rock alteration and directly associated with gold deposition; (4) geochemical signature, with mineralization showing consistent metal associations (Au–Ag–As–Sb and low base metal), which is compatible with metamorphic fluids.     

Ore petrology,hydrothermal alteration,fluid inclusions,and sulfur stable isotopes of the Milin Kamak intermediate sulfidation epithermal Au-Ag deposit in Western Srednogorie,Bulgaria

The Milin Kamak gold-silver deposit is located in Western Srednogorie zone, 50 km west of Sofia, Bulgaria. This zone belongs to the Late Cretaceous Apuseni-Banat-Timok-Srednogorie magmatic and metallogenic belt. The deposit is hosted by altered trachybasalt to andesitic trachybasalt volcanic and volcanoclastic rocks with Upper Cretaceous age, which are considered to be products of the Breznik paleovolcano. Milin Kamak is the first gold-silver intermediate sulfidation type epithermal deposit recognized in Srednogorie zone in Bulgaria. It consists of eight ore zones with lengths ranging from 400 to 1000 m, widths from several cm to 3–4 m, rarely to 10–15 m, an average of 80–90 m depth (a maximum of 200 m) and dip steeply to the south. The average content of gold is 5.04 g/t and silver – 13.01 g/t. The styles of alteration are propylitic, sericite, argillic, and advanced argillic. Ore mineralization consists of three stages. Quartz-pyrite stage I is dominated by quartz, euhedral to subhedral pyrite, trace pyrrhotite and hematite in the upper levels of the deposit. Quartz-polymetallic stage II is represented by major anhedral pyrite, galena, Fe-poor sphalerite; minor chalcopyrite, tennantite, bournonite, tellurides and electrum; and trace pyrrhotite, arsenopyrite, marcasite. Gangue minerals are quartz and carbonates. The carbonate-gold stage III is defined by deposition of carbonate minerals and barite with native gold and stibnite.Fluid inclusions in quartz are liquid H₂O-rich with homogenization temperature (T_h) ranging from 238 to 345 °C as the majority of the measurements are in the range 238–273 °C. Ice-melting temperatures (T_m) range from −2.2 to −4.1 °C, salinity – from 3.7 to 6.6 wt.% NaCl equiv. These measurements imply an epithermal environment and low- to moderate salinity of the ore-forming fluids.δ³⁴S values of pyrite range from −0.49 to +2.44‰. The average calculated δ³⁴S values are 1.35‰. The total range of δ³⁴S values for pyrite are close to zero suggesting a magmatic source for the sulfur.     

The Nadun Cu–Au mineralization,central Tibet: Root of a high sulfidation epithermal deposit

A new high sulfidation epithermal Cu–Au occurrence (Nadun) has been discovered adjacent to the Cretaceous Duolong porphyry Cu–Au deposit within the Bangong–Nujiang metallogenic belt, central Tibet. The Nadun Cu–Au mineralization is hosted in a tectonic–hydrothermal breccia with advanced argillic alteration, which occurs above sandstone, associated with quartz–pyrite veins. The granodiorite porphyry with strong argillic alteration yields a zircon U–Pb age of 119.1 ± 1.3 Ma, whereas the weakly argillic granodiorite porphyry intruded into the breccia has a younger age of 116.1 ± 1.3 Ma. This indicates that Cu–Au epithermal mineralization likely occurred between ~ 116 Ma and ~ 119 Ma, consistent with the duration of magmatic–hydrothermal activity at Duolong (~ 115–118 Ma), and providing evidence that Nadun and Duolong were formed during the same event. Moreover, the Nadun and Duolong porphyries have similar Hf isotopic compositions (εHf(t) values ranging from − 8.8 to 8.1; mean = 5.0 ± 1.1, n = 32), likely indicating that the deposits are comagmatic. In addition, boiling assemblages in vapor-rich inclusions coexisting with brines occur in early stage quartz–pyrite veins, and likely record phase separation at a temperature of > 550–300 °C and pressure of 700–110 bars. Most liquid-rich fluid inclusions formed at the breccia stage show similar salinity (1.7–19.3 wt.% NaCl equiv) to vapor-rich inclusions from the underlying quartz–pyrite veins, likely indicating vapor contraction during cooling at elevated presssure. This suggests that quartz–pyrite veins may act as conduits for ore-forming fluid traveling from the porphyry to the epithermal hydrothermal system. O and H isotopic compositions (δ¹⁸O_fluid = 0.42–9.71‰ and δD = − 102 to − 66‰) suggest that ore-forming fluids are dominantly from a magmatic source with a minor addition of meteoric water at a later stage. The S and Fe isotope compositions of sulfides (δ³⁴S = − 5.9 to 0.5‰ and δ⁵⁷Fe = − 2.15 to 0.17‰) decrease from the quartz–pyrite vein to breccia ore, indicating that ore-forming fluids gradually become SO₄²-enriched and relatively oxidized. This body of evidence suggests that the Nadun Cu–Au mineralization may represent the root of a high sulfidation epithermal deposit.     

Geology of the Jiama porphyry copper–polymetallic system,Lhasa Region,China

The Jiama deposit, located in the eastern part of the well-known Gangdese Metallogenic Belt on the Tibetan Plateau, is the largest porphyry Cu–polymetallic system in the region, with the largest exploration budget, and is economically viable in the Gangdese Belt to undergo large-scale development. The deposit is well preserved and has experienced little erosion. The proven resources of the deposit are 7.4 Mt Cu, 0.6 Mt Mo, 1.8 Mt Pb + Zn, 6.65 Moz Au, and 360.32 Moz Ag. The results presented in this paper are based on geological and tectonic mapping, geological logging, and other exploration work performed by members of the Jiama Exploration Project Team over a period of 6 years. We propose that the Jiama porphyry Cu–polymetallic system is composed of skarn Cu–polymetallic, hornfels Cu–Mo, porphyry Mo ± Cu, and distal Au mineralization. The development of skarn Cu–polymetallic orebodies at the Jiama deposit was controlled mainly by the contact zone between porphyries and marbles, an interlayer detachment zone, and the front zone of a gliding nappe structure. The hornfels Cu–Mo and porphyry Mo ± Cu orebodies were controlled mainly by a fracture system related to intrusions, and the distal Au mineralization resulted from late-stage hydrothermal alteration.On the basis of field geological logging, optical microscopy, and chemical analysis, we verify that the alteration zones in the Jiama deposit include potassic, phyllic, propylitic, and argillic alteration, with a local lithocap, as well as endoskarn and exoskarn zones. The endoskarn occurs mainly as epidote alteration in quartz diorite porphyry and granite porphyry, and is cut by massive andradite veins. The exoskarn includes garnet–pyroxene and wollastonite skarn, in which the mineralogy and mineral chemical compositions display an outward zonation with respect to the source porphyry. From the proximal skarn to the intermediate skarn to the distal skarn, the garnet/pyroxene ratio varies from > 20:1 to ~ 10:1 to ~ 5:1, the garnet color varies from red-brown to brown-green to green-yellow, and the average composition of garnet varies from Ad_80.1Gr_18.9(Sp + Py)_1.0 to Ad_76.3Gr₂₃(Sp + Py)_0.7 to Ad_59.5Gr_39.5(Sp + Py)_1.0, respectively. The pyroxene is not as variable in composition as the garnet, and is primarily light green to white diopside with a maximum hedenbergite content of ~ 20% and an average composition of Di_88.6Hd_8.9Jo_2.5. From the proximal skarn to the intermediate skarn to the distal skarn, the mineralization changes from Cu–Mo to Cu ± Mo to Pb–Zn ± Cu ± Au ores, respectively. The wollastonite skarn displays no zonation and hosts mainly bornite mineralization. The Cu and Mo mineralization is closely related to the potassic and phyllic zones in the porphyry–hornfels.Zircons from four mineralized porphyries yield U–Pb ages of 15.96 ± 0.5 Ma, 15.72 ± 0.14 Ma, 15.59 ± 0.09 Ma, and 15.48 ± 0.08 Ma. The Re–Os ages of molybdenite from the skarn, hornfels, and porphyry are 15.37 ± 0.15 Ma, 14.67 ± 0.37 Ma, and 14.66 ± 0.27 Ma, respectively. The present results are consistent with the findings of previous research on fluid inclusions, isotopes, and other such aspects. On the basis of the combined evidence, we propose a porphyry Cu–polymetallic system model for the Jiama deposit and suggest a regional exploration strategy that can be applied to prospecting for porphyry-skarn mineralization in the Lhasa area.     

The possible synglaciogenic Ediacaran hematitic banded iron salt formation (BISF) at Hormuz Island,southern Iran: Implications for a new style of exhalative hydrothermal iron-salt system

The Ediacaran BISF at Hormuz Island is a newly identified glaciogenic iron-salt deposit in the Tethyan margin of Gondwana. The BISF was formed by synchronous riftogenic A-type submarine felsic volcanism and evaporate deposition. The mineralization occurs in a proximal felsic tuff cone and jaspilitic distal zones and contains 1 million tonne of hematite-rich ore with an average grade of 58% Fe. The ore structure shows cyclicity of macrobandings, mesobandings and microbandings of anhydrite, halite, hematite and chert, which marks a new record in BIFs geohistory. The alteration minerals in the proximal and distal zones are actinolite, ripidolite, epidote, sericite, tourmaline, clinochlore, anhydrite and clay minerals. The occurrence of metamorphosed polygenetic bullet-shape dropstones in BISF attests that there was probably a continuous process of ice melting, episodic submarine volcanism and exhalative hydrothermal banded iron salt formation during the Late Ediacaran time. The non-metamorphosed Neoproterozoic stratigraphy, the presence of genus Collenia, U-Pb dating (558 ± 7 Ma) and the marked negative δ¹³C excursion in cap carbonates are representative of Late Ediacaran glaciation, which has been identified worldwide. The REE+Y display light REE enrichment, unusually strong Tb-Tm anomaly, a weak positive Y anomaly, but no distinguished Eu and Ce anomalies, reflecting the glaciogenic nature of the BISF. The contents of Zr, Hf, Nb, Ta, Th, La, Ce and Y in BISF, dropstones, halite and cap carbonates are similar to those of the Neoproterozoic glaciogenic BIFs. Also, the Ni/Fe, P/Fe ratios and Fe/Ti – Al/Al + Fe + Mn + Ca + Na + K diagram suggest an exhalative hydrothermal Ediacaran-type BISF. The absence of brecciated magnetite in the ore association and the low contents of copper (9–493 ppm) and gold (<5–8 ppb) are not in favor of the IOCG – Kiruna-type iron oxide ores. The co-paragenesis of hematite with several alteration minerals, in particular actinolite, tourmaline and anhydrite, indicates that the exhalative hydrothermal fluids were generated by the interaction of seawater with the felsic rocks and sediments at about 200–500 °C. The interaction of seawater with felsic magma and sediments led to the formation of Mg-rich alteration minerals, leaching Si, Fe, Mn and other elements and forming the potential ore fluids. It is highlighted that the A-type alkaline submarine felsic volcanism could be considered as an exploration target for BISF.     

The Guelb Moghrein Cu–Au deposit: Neoarchaean hydrothermal sulfide mineralization in carbonate-facies iron formation

The Guelb Moghrein copper–gold deposit in the Islamic Republic of Mauritania reopened in 2006 and has produced copper concentrate and gold since then. The deposit is hosted in Neoarchaean–Palaeoproterozoic Fe–Mg carbonate-dominated metamorphic rocks interpreted as carbonate-facies iron formation. It forms tabular orebodies controlled by shear zones in the hanging wall and footwall of this meta-iron formation. Copper and gold are hosted in a complex sulfide ore in tectonic breccia replacing Fe–Mg carbonate and magnetite. Hydrothermal monazite dates the mineralization at 2492 ± 9 Ma. Two types of aqueous fluid inclusions suggest fluid mixing at 0.75–1.80 kbar and ~ 410 °C as the mineralization and precipitation mechanism, which is temporally coincident with regional retrograde metamorphism at 410 ± 30 °C (garnet-biotite). Distal alteration zones are enriched in K, Rb and Cu, whereas orebodies are depleted in K, Rb, Sr and Ba. The copper–gold mineralization at Guelb Moghrein formed during retrograde shearing in metamorphic rocks and contemporaneous hydrothermal alteration. The stable isotope signature of alteration and ore minerals suggest an external crustal fluid source. Fluids were focused in the reactive and competent meta-iron formation. Potassium alteration, magnetite and copper–gold mineralization suggest an IOCG mineral system akin similar deposits in Australia and Brazil.     

Geological,geochemical, and geochronological characteristics of Caledonian W–Sn mineralization in the Baiganhu orefield,southeastern Xinjiang,China

The newly discovered large-scale Baiganhu W–Sn orefield, consisting of the Kekekaerde, Baiganhu, Bashierxi, and Awaer deposits, is located in Ruoqiang County, southeastern Xinjiang, China. These deposits comprise mainly three types of W–Sn mineralization: early-stage skarn-type, middle-stage greisen-type, and late-stage quartz-vein-type. In this study, we classified seven major vertical zones on the basis of petrographic characteristics, roughly from the bottom of the parental granitic intrusions upward, as (A) fresh syenogranite, (B) argillic alteration, (C) muscovite-dominated greisenization, (D) tourmaline-dominated greisenization, (E) marginal facies (including K-feldspar pegmatite and fine-grained granite), (F) aplitic apophysis, and (G1) skarn or (G2) infilled silification zones. According to the alteration–mineralization assemblages and cross-cutting relationships, five stages of mineralization are recognized in the orefield (I, skarn stage; II, greisen stage; III, quartz vein stage; IV, argillic alteration stage; and V, supergene stage), and reverse alteration zonation in the altered intrusion is also observed.The W–Sn deposits are spatially associated with syenogranite, which is part of the Caledonian Bashierxi magmatic series. Laser ablation–inductively coupled plasma–mass spectrometry (LA-ICP-MS) zircon U–Pb dating of the syenogranite yields a weighted mean ²⁰⁶Pb/²³⁸U age of 413.6 ± 2.4 Ma (MSWD = 0.36, n = 30). Hydrothermal muscovite from three samples associated with W–Sn mineralization yields plateau ⁴⁰Ar/³⁹Ar ages of 411.7 ± 2.6 Ma (MSWD = 0.21), 412.8 ± 2.4 Ma (MSWD = 0.22), and 413.8 ± 2.6 Ma (MSWD = 0.22), which is consistent with the zircon U–Pb age, thus indicating a temporal link between the emplacement of the syenogranite and the W–Sn mineralization. Our age data and previously published ages, along with geochemical data, for the granitoids in the Bashierxi magmatic series show a nearly contemporaneous evolution of A- and S-type granites, which were emplaced in a post-orogenic setting at ca. 432–413 Ma. As compared with the A-type granites, the syenogranites with S-type affinities probably resulted from a lower degree of partial melting of metagreywackes, which was more likely to be enriched in the ore-forming elements W and Sn, as well as volatiles such as B and H₂O. In addition, the syenogranites exhibit low oxidation states and underwent high degrees of factional crystallization, both of which favor post-magmatic W–Sn mineralization. We suggest that more attention should be given to buried syenogranites of S-type affinities during mineral exploration in this area, and that the proposed model of a vertical alteration zoning can act as a guide to the targeting of similar ore systems.     

Unveiling the hydrothermal mineralogy of the Chapi Chiara gold prospect,Peru, through reflectance spectroscopy,geochemical and petrographic data

Southern Peru contains important epithermal Au–Ag (± base metals) deposits, such as Canahuire, Tucari, Santa Rosa, Caylloma, Shila and Paula. The Chapi Chiara gold prospect is located in this region and is part of a paleo-stratovolcano of the Upper Miocene–Pliocene. The hydrothermal alteration of the prospect was characterized based on spectroradiometric data, geochemistry and petrography. The mineralogical data, interpreted based on reflectance spectroscopy, were spatialized using the sequential indicator simulation technique for producing probabilistic maps of alteration. The inner part of the paleo-stratovolcano (SW sector) is marked by three main cores of advanced argillic alteration (AAA) (quartz–alunite supergroup minerals–kaolinite–dickite ± topaz ± pyrophyllite ± diaspore) associated with topographic highs. The AAA1 core is surrounded by argillic alteration (quartz–illite–paragonitic illite–smectite ± pyrite) and propylitic alteration (quartz–plagioclase–chlorite–calcite–epidote–smectite ± kaolinite ± pyrite ± chalcopyrite ± magnetite). The central sector of the prospect, situated in the NE flank of the paleo-stratovolcano, is characterized by hydrothermal breccias structured towards N65E. The main mineral phases comprise quartz and abundant pyrite, sometimes with traces of As. Anomalous geochemical values of Ag, As, Bi, Hg, Se, Sb and Te coincide with high gold contents in this sector of the prospect. Jarosite and goethite are evidence of a subsequent supergene event. Based on the mineralogical characterization, we conclude the existence of a high sulfidation epithermal system in Chapi Chiara. Hypogene minerals of higher temperature in the SW sector of the prospect, such as diaspore, pyrophyllite and topaz in the AAA zone, and epidote in the propylitic alteration zone, can reveal that the system is currently in a relatively deep erosion level, suggesting its proximity in relation to the interface between a deep epithermal system and a mesothermal system.     

Nature of ore-forming fluid and formation conditions of BIF-hosted gold mineralization in the Archean Amalia Greenstone Belt,South Africa: Constraints from fluid inclusion and stable isotope studies

Orogenic gold mineralization in the Amalia greenstone belt is hosted by oxide facies banded iron-formation (BIF). Hydrothermal alteration of the BIF layers is characterized by chloritization, carbonatization, hematization and pyritization, and quartz-carbonate veins that cut across the layers. The alteration mineral assemblages consist of ankerite-ferroan dolomite minerals, siderite, chlorite, hematite, pyrite and subordinate amounts of arsenopyrite and chalcopyrite. Information on the physico-chemical properties of the ore-forming fluids and ambient conditions that promoted gold mineralization at Amalia were deduced from sulfur, oxygen and carbon isotopic ratios, and fluid inclusions from quartz-carbonate samples associated with the gold mineralization.Microthermometric and laser Raman analyses indicated that the ore-forming fluid was composed of low salinity H₂O-CO₂ composition (~3 wt% NaCl equiv.). The combination of microthermometric data and arsenopyrite-pyrite geothermometry suggest that quartz-carbonate vein formation, gold mineralization and associated alteration of the proximal BIF wall rock occurred at temperature-pressure conditions of 300 ± 30 °C and ∼2 kbar. Thermodynamic calculations at 300 °C suggest an increase in fO₂ (10⁻³²–10⁻³⁰ bars) and corresponding decrease in total sulfur concentration (0.002–0.001 m) that overlapped the pyrite-hematite-magnetite boundary during gold mineralization. Although hematite in the alteration assemblage indicate oxidizing conditions at the deposit site, the calculated low fO₂ values are consistent with previously determined high Fe/Fe + Mg ratios (>0.7) in associated chlorite, absence of sulfates and restricted positive δ³⁴S values in associated pyrite. Based on the fluid composition, metal association and physico-chemical conditions reported in the current study, it is confirmed that gold in the Amalia fluid was transported as reduced bisulfide complexes (e.g., Au(HS)₂⁻). At Amalia, gold deposition was most likely a combined effect of increase in fO₂ corresponding to the magnetite-hematite buffer, and reduction in total sulfur contents due to sulfide precipitation during progressive fluid-rock interaction.The epigenetic features coupled with the isotopic compositions of the ore-forming fluid (δ³⁴S_ΣS = +1.8 to +2.3‰, δ¹⁸O_H2O = +6.6 to +7.9‰, and δ¹³C_ΣC = −6.0 to −7.7‰ at 300–330 °C) are consistent with an externally deep-sourced fluid of igneous signature or/and prograde metamorphism of mantle-derived rocks.     

Origin of a barite-sulfide ore deposit in the Mykonos intrusion,cyclades: Trace element,isotopic, fluid inclusion and raman spectroscopy evidence

The polymetallic Mykonos vein system in the Cyclades, Greece, consists of 15 tension-gashes filled with barite, quartz, pyrite, sphalerite, chalcopyrite and galena in ca. 13.5 Ma, I-type, Mykonos monzogranite. Zones of silica and chlorite–muscovite alteration are associated with the veins and overprint pervasive silicification, phyllic and argillic alteration that affected large parts of the monzogranite. The mineralization cements breccias and consists of an early barite–silica–pyrite–sphalerite–chalcopyrite assemblage followed by later argentiferous galena. A combination of fluid inclusion and stable isotope data suggests that the barite and associated mineralization were deposited from fluids containing 2 to 17 wt.% NaCl equivalent, at temperatures of ~ 225° to 370 °C, under a hydrostatic pressure of ≤ 100 bars. The mineralizing fluids boiled and were saturated in H₂S and SO₂.Calculated δ¹⁸O_H2O and δD_H2O, initial ⁸⁷Sr/⁸⁶Sr isotope compositions and the trace and REEs elements contents are consistent with a model in which the mineralizing fluids were derived during alteration of the Mykonos intrusion and subsequently mixed with Miocene seawater. Heterogeneities in the calculated δ³⁴S_SO4^− 2 and δ³⁴S_H2S compositions of the ore fluids indicate two distinct sources for sulfur, namely of magmatic and seawater origin, and precipitation due to reduction of the SO₄^− 2 during fluid mixing. The physicochemical conditions of the fluids were pH = 5.0 to 6.2, logf_S2 = − 13.8 to − 12.5, logf_O2 = − 31.9 to − 30.9, logf_H2S(g) = − 1.9 to − 1.7, logf_Te2 = − 7.9 and logα(SO₄^− 2_(aq)/H₂S_(aq)) = + 2.6 to + 5.5. We propose that retrograde mesothermal hydrothermal alteration of the Mykonos monzogranite released barium and silica from the alkali feldspars. Barite was precipitated due to mixing of SO₄^− 2-rich Miocene seawater with the ascending Ba-rich magmatic fluid venting upwards in the pluton.     

Variation of copper isotopes in chalcopyrite from Dabu porphyry Cu-Mo deposit in Tibet and implications for mineral exploration

The study presents copper (Cu) isotope data of mineral separates of chalcopyrite from four drill core samples in the Miocene Dabu porphyry Cu-Mo deposit formed in a post-collisional setting in the Gangdese porphyry copper belt, southern Tibet. Copper isotope values in hypogene chalcopyrite range from –1.48‰ to +1.12‰, displaying a large variation of up to 2.60‰, which demonstrates Cu isotope fractionation at high-temperature during hydrothermal evolution. The majority of measured chalcopyrite isotopic compositions show a gradual increasing trend from –1.48‰ to +1.12‰ with the increase of drilling depth from 130m to 483m, as the alteration assemblages change from potassic to phyllic. Similarly, the other δ⁶⁵Cu values (δ⁶⁵Cu = ((⁶⁵Cu/⁶³Cu)_sample/(⁶⁵Cu/⁶³Cu)_standard − 1) × 1000) of the chalcopyrite show a gradual increasing trend from −1.48‰ to +0.59‰ with the decrease of drilling depth from 130 m to 57 m, as the alteration assemblages change from potassic, phyllic, through argillic to relatively fresh. These observations suggest a genetic link between Cu isotope variation and silicate alteration assemblages formed at different temperatures, indicative of a Rayleigh precipitation process resulting in the large variation of δ⁶⁵Cu values at Dabu. In general, samples closest to the center of hydrothermal system dominated by high-temperature potassic alteration are isotopically lighter, whereas samples dominated by low-temperature phyllic alteration peripheral to the center are isotopically heavier. The predicted flow pathways of hydrothermal fluids are from No. 0 to No. 3 exploration line, and the lightest δ⁶⁵Cu values are the most proximal to the hydrothermal source. Finally, we propose that the northwest side of the No. 0 exploration line has high potential for hosting undiscovered orebodies. The pattern of Cu isotope variation in conjunction with the features of silicate alteration in porphyry system can be used to trace the hydrothermal flow direction and to guide mineral exploration.     

Geology,geochemistry, and geochronology of Fe-oxide Cu (± Au) mineralization associated with Şamlı pluton,western Turkey

The Şamlı (Balıkesir) Fe-oxide Cu (± Au) deposit, one of several iron (+ Cu ± Au) deposits in western Turkey, is hosted by porphyritic rocks of the multi-phase Şamlı pluton and metapelitic–metadiabasic rocks of Karakaya Complex. Two successive mineralization events are recognized in the area as; i) early magnetite and sulfide and ii) late hematite–goethite-native copper (± Au). Alteration associated with the mineralization in Şamlı is characterized by four distinct mineralogical assemblages. They are, in chronological order of formation, (1) plagioclase–early pyroxene (± scapolite), (2) garnet–late pyroxene, (3) chlorite–epidote, and (4) chalcedony–calcite alteration. Geochemical, isotopic (Sr, Nd, O, S) and geochronological (Ar–Ar) data from alteration and magmatic rocks suggest a temporal and genetic link between the multiphase Şamlı pluton and the hydrothermal system that controls the Fe-oxide-Cu (± Au) mineralization. ⁴⁰Ar/³⁹Ar geochronology on hornblende and biotite separates of the Şamlı pluton yielded an age range between 23.20 ± 0.50 and 22.42 ± 0.11 Ma, overlapping with ⁴⁰Ar/³⁹Ar age of 22.34 ± 0.59 Ma from alteration.The close spatial and temporal associations of Şamlı mineralization with porphyritic intrusions, pervasive Ca-rich alteration (calcic plagioclase, andraditic garnet, diopsidic pyroxene, scapolite, and epidote) are considered as common features akin to calcic assemblages in typical IOCG deposits. Besides abundant low-Ti (≤ 0.5%) magnetite/hematite, high Cu–moderate Au (up to 8.82 ppm) association, structural control and lithologic controls of mineralization, low S-sulfide content (chalcopyrite > pyrite) in the deposit; and the derivation of causative magma from subduction-modified subcontinental lithospheric mantle under a transpressional to transtensional regime, are collectively considered as the features in favor of IOCG-type mineralization for the Şamlı deposit.     

Some new data on the genesis of the Linghou Cu–Pb–Zn polymetallic deposit—Based on the study of fluid inclusions and C–H–O–S–Pb isotopes

The Linghou deposit, located near Hangzhou City of Zhejiang Province, eastern China, is a medium-sized polymetallic sulfide deposit associated with granitic intrusion. This deposit is structurally and lithologically controlled and commonly characterized by ore veins or irregular ore lenses. In this deposit, two mineralization events were identified, of which the former produced the Cu–Au–Ag orebodies, while the latter formed Pb–Zn–Cu orebodies. Silicification and calc-silicate (skarn type), phyllic, and carbonate alternation are four principal types of hydrothermal alteration. The early Cu–Au–Ag and late Pb–Zn–Cu mineralizations are characterized by quartz ± sericite + pyrite + chalcopyrite + bornite ± Au–Ag minerals ± magnetite ± molybdenite and calcite + dolomite + sphalerite + pyrite + chalcopyrite + galena, respectively. Calcite clusters and calcite ± quartz vein are formed during the late hydrothermal stage.The NaCl–H₂O–CO₂ system fluid, coexisting with NaCl–H₂O system fluid and showing the similar homogenization temperatures (385 °C and 356 °C, respectively) and different salinities (16.89–21.68 wt.% NaCl eqv. and 7.70–15.53 wt.% NaCl eqv.), suggests that fluid immiscibility occurred during the Cu–Au–Ag mineralization stage and might have given rise to the ore-metal precipitation. The ore-forming fluid of the Pb–Zn–Cu mineralization mainly belongs to the NaCl–H₂O–CO₂ system of high temperature (~ 401 °C) and mid-high salinity (10.79 wt.% NaCl eqv.).Fluids trapped in the quartz-chalcopyrite vein, Cu–Au–Ag ores, Pb–Zn–Cu ores and calcite clusters yielded δ¹⁸O_H2O and δD values varying from 5.54‰ to 13.11‰ and from − 71.8‰ to − 105.1‰, respectively, indicating that magmatic fluids may have played an important role in two mineralization events. The δ¹³C_PDB values of the calcite change from − 2.78‰ to − 4.63‰, indicating that the CO₃^2 − or CO₂ in the ore-forming fluid of the Pb–Zn–Cu mineralization was mainly sourced from the magmatic system, although dissolution of minor marine carbonate may have also occurred during the ore-forming processes. The sulfide minerals have homogeneous lead isotopic compositions with ²⁰⁶Pb/²⁰⁴Pb ranging from 17.958 to 18.587, ²⁰⁷Pb/²⁰⁴Pb ranging from 15.549 to 15.701, and ²⁰⁸Pb/²⁰⁴Pb ranging from 37.976 to 39.052, indicating that metallic elements of the Linghou deposit came from a mixed source involving mantle and crustal components.Based on geological evidence, fluid inclusions, and H–O–C–S–Pb isotopic data, the Linghou polymetallic deposit is interpreted as a high-temperature, skarn-carbonate replacement type. Two types of mineralization are both related to the magmatic–hydrothermal system, with the Cu–Au–Ag mineralization having a close relationship with granodiorite.     

Mineral chemistry of hydrothermal biotite from the Kahang porphyry copper deposit (NE Isfahan), Central Province of Iran

The Kahang porphyry Cu deposit, located northeast of Isfahan city in central of Iran, is associated with a composite Miocene stock and ranges in composition from diorite through granodiorite to quartz-monzonite. Field observations and petrographic studies show that the emplacement of the Kahang stock occurred in several pulses, each associated with its related hydrothermal activity. Early hydrothermal alteration started with a potassic style in the central part of the system and produced a secondary biotite–K-feldspar–magnetite assemblage accompanied by chalcopyrite and pyrite mineralization. Propylitic alteration that took place at the same time as the potassic alteration occurred in the peripheral portions of the stock. Subsequent phyllic alteration overprinted earlier potassic and propylitic alterations. Biotite grains from the potassic and phyllic zones show distinct chemical compositions. The FeO, TiO₂, MnO, K₂O, and Na₂O concentrations in biotite from the phyllic alteration zone are lower than those from the potassic alteration zone. The F and Cl contents of biotite from the potassic alteration zone display relatively high positive correlation with the X_Mg. The fluorine intercept values [IV(F)] from the potassic and phyllic alteration zones are strongly correlated with the fluorine/chlorine intercept values [IV(F/Cl)]. Biotite geothermometry for the potassic and phyllic alteration zones, based on the biotite geothermometer of Beane (1974), yields a temperature range of 422° to 437 °C (mean = 430 °C) and 329° to 336 °C (mean = 333 °C), respectively. The position of data in log (X_F/X_OH) ratio vs. X_Mg and X_Fe diagram suggests that biotite formed under dissimilar composition and temperature conditions in the potassic and phyllic alteration zones. Calculated log fugacity ratios of (fH₂O/fHF), (fH₂O/fHCl), and (fHF/fHCl) show that hydrothermal fluids associated with the potassic alteration were distinctively different from those fluids associated with the phyllic alteration zone at Kahang porphyry Cu deposit. The results of this research indicate that the chemistry of biotite is related to the chemical composition of the magma and the prevailing physical conditions during crystallization.     

Magmatic-vapor expansion and the formation of high-sulfidation gold deposits: Structural controls on hydrothermal alteration and ore mineralization

High-sulfidation copper–gold lode deposits such as Chinkuashih, Taiwan, Lepanto, Philippines, and Goldfield, Nevada, formed within 1500 m of the paleosurface in volcanic terranes. All underwent an early stage of extensive advanced argillic silica–alunite alteration followed by an abrupt change to spatially much more restricted stages of fracture-controlled sulfide–sulfosalt mineral assemblages and gold–silver mineralization. The alteration as well as ore mineralization stages of these deposits were controlled by the dynamics and history of syn-hydrothermal faulting.At the Sulfate Stage, aggressive advanced argillic alteration and silicification were consequent on the in situ formation of acidic condensate from magmatic vapor as it expanded through secondary fracture networks alongside active faults. The reduction of permeability at this stage due to alteration decreased fluid flow to the surface, and progressively developed a barrier between magmatic-vapor expansion constrained by the active faults and peripheral hydrothermal activity dominated by hot-water flow. In conjunction with the increased rock strength resulting from alteration, subsequent fault-slip inversion in response to an increase in compressional stress generated new, highly permeable fractures localized by the embrittled, altered rock. The new fractures focused magmatic-vapor expansion with much lower heat loss so that condensation occurred. Sulfide Stage sulfosalt, sulfide, and gold–silver deposition then resulted from destabilization of vapor phase metal species due to vapor decompression through the new fracture array. The switch from sulfate to sulfide assemblages is, therefore, a logical consequence of changes in structural permeability due to the coupling of alteration and fracture dynamics rather than to changes in the chemistry of the fluid phase at its magmatic source.     

Mineral chemistry and geochemical behavior of hydrothermal alterations associated with mafic intrusive-related Au deposits at the Atud area,Central Eastern Desert,Egypt

Vein-type gold deposits in the Atud area are related to the metagabbro–diorite complex that occurred in Gabal Atud in the Central Eastern Desert of Egypt. This gold mineralization is located within quartz veins and intense hydrothermal alteration haloes along the NW–SE brittle–ductile shear zone, as well as along the contacts between them. By using the mass balance calculations, this work is to determine the mass/volume gains and losses of the chemical components during the hydrothermal alteration processes in the studied deposits. In addition, we report new data on the mineral chemistry of the alteration minerals to define the condition of the gold deposition and the mineralizing fluid based on the convenient geothermometers. Two generations of quartz veins include the mineralized grayish-to-white old vein (trending NW–SE), and the younger, non-mineralized milky white vein (trending NE–SW). The ore minerals associated with gold are essentially arsenopyrite and pyrite, with chalcopyrite, sphalerite, enargite, and goethite forming during three phases of mineralization; first, second (main ore), and third (supergene) phases. Three main hydrothermal alteration zones of mineral assemblages were identified (zones 1–3), placed around mineralized and non-mineralized quartz veins in the underground levels. The concentrations of Au, Ag, and Cu are different from zone to zone having 25–790 ppb, 0.7–69.6 ppm, and 6–93.8 ppm; 48.6–176.1 ppb, 0.9–12.3 ppm, and 39.6–118.2 ppm; and 53.9–155.4 ppb, 0.7–3.4 ppm, and 0.2–79 ppm for zones 1, 2, and 3, respectively.The mass balance calculations and isocon diagrams (calculated using the GEOISO-Windows program) revealed the gold to be highly associated with the main mineralized zone as well as sericitization/kaolinitization and muscovitization in zone 1 more than in zones 2 and 3. The sericite had a higher muscovite component in all analyzed flakes (average X_Ms = 0.89), with 0.10%–0.55% phengite content in wall rocks and 0.13%–0.29% phengite content in mineralized quartz veins. Wall rocks had higher calcite (CaCO₃) contents and lower MgCO₃ and FeCO₃ contents than the quartz veins. The chlorite flakes in the altered wall rocks were composed of pycnochlorite and ripidolite, with estimated formation temperatures of 289–295 °C and 301–312 °C, respectively. Albite has higher albite content (95.08%–99.20%) which occurs with chlorite in zone 3.     

The role of evaporites in the formation of magnetite–apatite deposits along the Middle and Lower Yangtze River,China: Evidence from LA-ICP-MS analysis of fluid inclusions

Numerous magnetite–apatite deposits occur in the Ningwu and Luzong sedimentary basins along the Middle and Lower Yangtze River, China. These deposits are located in the contact zone of (gabbro)-dioritic porphyries with surrounding volcanic or sedimentary rocks and are characterized by massive, vein and disseminated magnetite–apatite ± anhydrite mineralization associated with voluminous sodic–calcic alteration. Petrologic and microthermometric studies on multiphase inclusions in pre- to syn-mineralization pyroxene and garnet from the deposits at Meishan (Ningwu basin), Luohe and Nihe (both in Luzong basin) demonstrate that they represent extremely saline brines (~ 90 wt.% NaCl_equiv) that were trapped at temperatures of about 780 °C. Laser ablation ICP-MS analyses and Raman spectroscopic studies on the natural fluid inclusions and synthetic fluid inclusions manufactured at similar P–T conditions reveal that the brines are composed mainly of Na (13–24 wt.%), K (7–11 wt.%), Ca (~ 7 wt.%), Fe (~ 2 wt.%), Cl (19–47 wt.%) and variable amounts of SO₄ (3–39 wt.%). Their Cl/Br, Na/K and Na/B ratios are markedly different from those of seawater evaporation brines and lie between those of magmatic fluids and sedimentary halite, suggesting a significant contribution from halite-bearing evaporites. High S/B and Ca/Na ratios in the fluid inclusions and heavy sulfur isotopic signatures of syn- to post-mineralization anhydrite (δ³⁴S_Anh = + 15.2 to + 16.9‰) and pyrite (δ³⁴S_Py = + 4.6‰ to + 12.1‰) further suggest a significant contribution from sedimentary anhydrite. These interpretations are in line with the presence of evaporite sequences in the lower parts of the sedimentary basins.The combined evidence thus suggests that the magnetite–apatite deposits along the Middle and Lower Yangtze River formed by fluids that exsolved from magmas that assimilated substantial amounts of Triassic evaporites during their ascent. Due to their Fe-oxide dominated mineralogy, their association with large-scale sodic–calcic alteration and their spatial and temporal associations with subvolcanic intrusions we interpret them as a special type of IOCG deposits that is characterized by unusually high contents of Na, Ca, Cl and SO₄ in the ore-forming fluids. Evaporite assimilation apparently led to the production of large amounts of high-salinity brine and thus to an enhanced capacity to extract iron from the (gabbro)-dioritic intrusions and to concentrate it in the form of ore bodies. Hence, we believe that evaporite-bearing sedimentary basins are more prospective for magnetite–apatite deposits than evaporite-free basins.     

Sulfidic and non-sulfidic indium mineralization of the epithermal Au–Cu–Zn–Pb–Ag deposit San Roque (Provincia Rio Negro,SE Argentina) — with special reference to the “indium window” in zinc sulfide

At San Roque in Patagonia's Rio Negro Province, Argentina, an In–Au–Cu–Zn–Pb–Ag mineralization (< 0.24 wt.% In, < 7 ppm Au, < 0.45 wt.% Cu, < 14.1 wt.% Zn, < 0.55 wt.% Pb, < 60 ppm Ag) is bound to lava, and volcaniclastics of Triassic through Jurassic age. The polymetallic sulfidic and non-sulfidic indium mineralization is attributed to the low-sulfidation (LS) to intermediate sulfidation (IS) epithermal type of mineralization. Its vein-type and stockwork mineralization developed at 39.2 bars under hydrostatic conditions, corresponding to a depth of 400 m below the water level of the paleoaquifer. In the redox-controlled hypogene mineralization, the temperature increased from 130 °C up to as much as 250 °C at depth, while the pH regime changed from slightly acidic near surface to more alkaline conditions around pH 8 at a depth of approximately 150 m. The monophase mineral associations composed of sphalerite, Ag–Bi-enriched and inclusion-free galena (< 1.7 wt.% Ag, < 3.7 wt.% Bi), chalcopyrite, pyrite, gold, silver, digenite, various In–Cu- and Pb–Zn–Ag “intermediate products”, wittichenite, roquesite, sakuraiite, dzhalindite, brochantite, antlerite, cerussite, and “manganomelane” in a quartz and muscovite-rich gangue have been subdivided into three different stages: (1) Stockwork mineralization of LS to IS epithermal type (hypogene), (2) quartz vein mineralization (hypogene), and (3) salar mineralization (supergene–hypogene).Salt–mud flats controlled the youngest mineralization with Mn, Li, Ca, Mg, V, Sr, Cu, Ag and In bound to oxides, hydroxides, sulfates and subordinate carbonates. The quartz vein mineralization is made up of oxides, hydroxides prevailing over sulfides and containing W, Fe, Au, As, Pb, In, and Cu. It formed at the passage from the vadose into the phreatic zones under oxidizing to slightly reducing conditions. The level marks the boiling level of the hydrothermal solutions involved in the mineralizing process. The hypogene stockwork mineralization is exclusively made up of sulfides containing Zn, Pb, Cu, In, Ag and Bi in the phreatic zones. It developed under reducing conditions. Indium is present at all levels within the volcanic rocks and has been derived from sphalerite rich in Cd (< 1.6 wt.% Cd), In (< 7.3 wt.% In) and Cu (< 7.2 wt.% Cu) while the Fe contents are moderate in sphalerite (< 6.8 wt.% Fe). Indium reached economic grade only through the segregation of a Cu–In–S phase in the “indium window” which is defined by a Cd content of sphalerite in the range 0.2–0.6 wt.% Cd. This concentration of In is controlled by the crystal morphology and the lattice parameters of the minerals involved. It is described as a two-stage process with interdiffusion processes in an Fe-enriched system (stage I) and zoned replacement in an Fe-poor system enriched in indium (stage II). Cu-bearing sphalerite decomposed into sphalerite poor in trace elements and into Cu–In-bearing sphalerite. Further indium concentration took place, when roquesite and sakuraiite decomposed along with an increase in oxygen pressure under hypogene and supergene conditions into dzhalindite. The physical–chemical conditions of the mineralogy and chemical changes in the system In–Cu–Zn–Cd observed in nature have been approximated based upon the results obtained during laboratory studies in material sciences that were focused on solar energy.