Iron oxide copper-gold (IOCG) mineralization at the Imiter inlier,Eastern Anti-Atlas,Morocco

The Imiter inlier at the eastern Anti-Atlas chain (Morocco) hosts a world-class epithermal Ag-Hg deposit, and several occurrences of sulfide-magnetite mineralization. These occurrences are confined to transcurrent faults that cut mildly to highly potassic I- and S-type granite intrusions (e.g., Igoudrane, Bou Teglimt, Taouzzakt and Bou Fliou).In this contribution, we present new field, petrographic and microanalytical data of the Bou Fliou sulfide-magnetite mineralization in the northwestern part of the Bou Teglimt granodiorite intrusion (567?±?6Ma). Field and microscopic investigations reveal pervasive silicification and potassic alteration associated with iron oxides-rich (>10?vol %) veins, stockworks, and breccias along NE-SW faults. The ore minerals are mainly magnetite, hematite, chalcopyrite, pyrite, sphalerite, Ag-galena, cobaltite, and less abundant Bi-sulfosalts (i.e., cosalite, galenobistmuthite, and llilanite-gustavite). The low-titanium iron oxides (magnetite and hematite), widespread iron-rich breccia, association with crustal scale fault zone, pervasive alteration, and overprinting mineral assemblages suggest a shallow level IOCG-style mineralization. High-order splays of the major fault zone could have provided effective traps for magmatic and basinal Cu and Zn-Pb hydrothermal fluids. The ～550 Ma intrusive phases in the region could have contributed by fluid, elements or heat in a local effective blumbing. The mineralogical and ore textural criteria reflecting ore formation at a realtively shallow crustal environment, but a fluid inclusion study is needed to characterize the ore fluids and mechanism of ore deposition.     

Hydrothermal fluid geochemistry at the Chah-Firuzeh porphyry copper deposit,Iran: Evidence from fluid inclusions

The Chah-Firuzeh porphyry copper deposit is located in 35 km north of Shahre Babak (Kerman province). It is associated with granodioriteic intrusive of Miocene age which intruded Eocene volcanosedimentary rocks. Copper mineralization was accompanied by both potassic and phyllic alteration. Field observations and petrographic studies demonstrate that the emplacement of Chah-Firuzeh pluton took place in several intrusive pulses, each with associated hydrothermal ore fluid formation that was also associated with hydrostatic pressure increasing respect to that of lithostatic pressure (and fracturing development-relative boiling) by circulated fluid. Copper is concentrated as a very early hydrothermal mineralized phase in the evolution of the hydrothermal system. Early hydrothermal alteration produced a potassic assemblage (orthoclase–biotite) in the central deep part of the stock. Alteration ore fluids could be classify into two groups of liquid-reach, containing solid phases, high temperature (390 to 500 °C) high salinity (more than 60 wt.% NaCl equiv.) and gas-rich, high temperature (311 to 570 °C), no solid phase and with low salinities. These magmatic source fluids illustrate sever boiling process and also are the responsible for the both potassic alteration, quartz group I and II veins and chalcopyrite deposition. Propylitic alteration occurred by the liquid-rich, low temperature (241 to 390 °C) and Ca-rich fluid with meteoric origin. Continuous decreasing temperature let the meteoric water diffusion into the system, mixed with magmatic fluids and descending the salinities down to the 1 wt.% NaCl equiv. and leaching the Cu from vein groups II and III by sever thermodynamic anarchies from potassic to the phyllic alteration zones. Phyllic alteration and copper leaching resulted from the inflow of oxidized and acidic meteoric waters with decreasing temperature of the system followed by the incursion of this fluid into and its convection in upper part of the system. A late episode of boiling occurred in the apical the phyllic zone, and was associated with significant copper deposition. Based on the field observation on sharp alteration and related mineralization, it is possible to conclude that all these procedures have been controlled by local faults that could be active even before the pluton injection. These faults and the new form ones (which have been formed after injection), could crash the hosted rocks, and act as physical dams to restrict and limit the mineralization in special strikes and zones within the Cah-Firuzeh ore deposit.     

Multi-stage hydrothermal processes involved in “low-sulfide” Cu(–Ni)–PGE mineralization in the footwall of the Sudbury Igneous Complex (Canada): Amy Lake PGE zone, East Range

The Amy Lake PGE zone is a “low-sulfide-type” Cu-(Ni-)PGE mineralization in the East Range footwall of the 1.85 Ga Sudbury Igneous Complex occurring in a 100-m-wide Sudbury Breccia belt that coincides with an impact-related major fracture zone (Bay Fault zone). Detailed hydrothermal alteration mapping, fluid inclusion, trace element, and stable isotope studies revealed a complex alteration and mineralization history in a multi-source, multi-stage Sudbury-related hydrothermal system. The two major stages of syn-Sudbury hydrothermal activity are characterized by similarly high-salinity, high-temperature fluids that are (1) locally derived from footwall granophyre bodies, and typified with high Ni/Cu and PGE/S ratios and high REE contents (magmatic–hydrothermal stage), and (2) a more voluminous Cu–Ni–PGE-rich fluid flux probably originated from the Sudbury Igneous Complex/footwall contact (hydrothermal stage). The second hydrothermal flux was introduced by brittle fractures in the area and resulted in a complex zonation of alteration assemblages and mineralization governed by local footwall composition. The Sudbury-related hydrothermal event was overprinted by shear-related epidote veining and calcite–chlorite replacement, both regionally present in the Sudbury structure. Based on analogies, the most important factors involved in the formation of hydrothermal low-sulfide mineralization are proposed to be (1) accumulation of PGE-enriched fluids, (2) large-scale brittle structures as conduits to these fluids, and (3) adequate host rock composition as a chemical trap resulting in sulfide and PGM precipitation. In environments meeting these criteria, hydrothermal PGE mineralization is known to have formed not only in the Sudbury footwall but also from mafic–ultramafic intrusions associated with primary magmatic PGE from several locations around the world.     

The Permo-Triassic vein and paleokarst ores in southwest Sardinia: Contribution of fluid inclusion studies to their genesis and paleoenvironment

This paper presents and discusses new fluid inclusion data on the temperatures, salinities and composition of mineralizing fluids in gangue and ore minerals in late- and post-Hercynian veins and paleokarsts both in the Iglesiente and Sulcis areas of southwest Sardinia. The results suggest that the fluids associated with mineralization are within the range normally recorded for Mississippi Valley-type deposits elsewhere in the world, both for homogenization temperatures (from below 60°C to 130°C for quartz, calcite, barite and dolomite, higher for fluorite) and salinities (5–24 equiv. wt% NaCl). High levels of CaCl₂ are also present in the fluids. Similar temperatures and salinities are shown by the dolomitic alteration of the karstified Cambrian limestones, which are the host rocks of the studied ore deposits, indicative of a common origin for both the alteration and mineralization.It is emphasized, however, that the exact origin of the ores is difficult to assess based on fluid inclusion analyses alone because the mentioned temperature range is not necessarily exclusive to either a purely supergene or hydrothermal origin. In view of the high salinities, however, the current opinion is that at least the dolomitization and a part of the ores could be related to late diagenetic processes involving connate waters from the neighboring Permo-Triassic lagoonal-evaporitic sediments.     

Fluid inclusion study of the bournac polymetallic (Sb-As-Pb-Zn-Fe-Cu...) vein deposit (montagne noire,France)

Mineralogical studies demonstrate that the Hercynian polymetallic antimony-rich deposit of Bournac can be described by four stages of ore deposition and one of partial ore remobilization. Fluid inclusion data permit calculation of the composition and temperature of the fluids associated with each stage of hydrothermal mineralization and concomitant wall-rock alteration. Stages I and II (Fe-As and Zn) are represented by moderate-salinity H₂O-CO₂-(NaCl) inclusions which correlate closely with early carbonate deposition. Stage III fluids which are responsible for the deposition of Pb-Sb ores are characterized by low-salinity H₂O-(NaCl) inclusions. During the final stage of mineralization (IV), corresponding to the main phase of stibnite deposition, abundant aqueous inclusions confirm the continued involvement of low-salinity fluids and the intense development of potassic clays and secondary silica in the wall rocks. Homogenization temperatures suggest that the whole cycle of mineralization took place during a gradual decrease in fluid temperature of 380°–140°C. Stibnite deposition is restricted to the interval of 230°–140°C thus confirming an essentially epithermal environment. Stage V (partial remobilization) is distinguished by the presence of high-salinity CaCl₂-rich inclusions which are tentatively related to Triassic barite mineralization in the region and therefore postdate the Bournac antimony ores. Homogenization temperatures for this stage range 140°–60°C.     

五台山区七图金矿的物源特征及矿床成因浅析

矿区成矿元素地球化学以及成矿流休的初步研究表明，五台山七图金矿的成矿物质（金，银）主要来源于围岩的滹沱群四集庄组粗碎屑岩组合，变质基性火山岩的去硫作用提供了金矿化的硫源，韧－脆性剪切事宾发育及活动是金矿化的动力学机制，成矿流体具有变质流体的性质，在变质基性火山岩中形成的蚀变岩与金矿化密切相关，矿床成因类型为沉积变质热液叠加型金矿床。     

Comparison between the fluid characteristics of the Rodalquilar and two neighbouring epithermal gold deposits in Spain

The operating Rodalquilar gold deposit and the abandoned Triunfo and Maria Josefa gold mines are located within the Sierra del Cabo de Gata volcanic field some 40 km east of Almeria in SE Spain. While the gold mineralization at Rodalquilar is mainly controlled by caldera-tectonics, vein structures at Triunfo and Maria Josefa are not. Wall-rock alteration at Triunfo and Maria Josefa is characterized by argillic alteration (illite/sericite, kaolinite). The alteration zonation around the gold-mineralized vein structures at Rodalquilar ranges from advanced argillic alteration (porous quartz, alunite, pyrophyllite, dickite) over argillic alteration into a regionally developed propylitization. Fluid inclusion studies from all three mines indicate that gold was deposited from low-salinity fluids (2–5 wt.% NaCl equivalent) between 170° and 250 °C. However, the hydrothermal system at Rodalquilar was fed by a second fluid source. High-salinity, halite and/or sylvite-bearing, liquid-rich, and vapour-dominated, CO₂-bearing fluid inclusions are assumed to be of magmatic origin. High sulfidation ore mineral assemblages at depth (covellite, enargite, tennantite) and part of the advanced argillic alteration can be related to these fluids. Thus, part of those features which attribute the Rodalquilar gold deposit to the acid-sulfate or high sulfidation type of epithermal gold deposits, stem from magmatically derived fluids which are typical for a porphyry environment, whereas gold mineralization at all three localities is associated with low-salinity fluids, probably of marine origin.     

Petrology,Geochemistry, and Fluid Inclusion Microthermometry of Sphalerite from the Laloki and Federal Flag Strata‐Bound Massive Sulfide Deposits,Papua New Guinea: Implications for Gold Mineralization

The Laloki and Federal Flag deposits are two of the many (over 45) polymetallic massive sulfide deposits that occur in the Astrolabe Mineral Field, Papua New Guinea. New data of the mineralogical compositions, mineral textures, and fluid inclusion studies on sphalerite from Laloki and Federal Flag deposits were investigated to clarify physiochemical conditions of the mineralization at both deposits. The two deposits are located about 2 km apart and they are stratigraphically hosted by siliceous to carbonaceous claystone and rare gray chert of Paleocene–Eocene age. Massive sulfide ore and host rock samples were collected from each deposit for mineralogical, geochemical, and fluid inclusion studies. Mineralization at the Laloki deposit consists of early‐stage massive sulfide mineralization (sphalerite‐barite, chalcopyrite, and pyrite–marcasite) and late‐stage brecciation and remobilization of early‐stage massive sulfides that was accompanied by late‐stage sphalerite mineralization. Occurrence of native gold blebs in early‐stage massive pyrite–marcasite‐chalcopyrite ore with the association of pyrrhotite‐hematite and abundant planktonic foraminifera remnants was due to reduction of hydrothermal fluids by the reaction with organic‐rich sediments and seawater mixing. Precipitation of fine‐grained gold blebs in late‐stage Fe‐rich sphalerite resulted from low temperature and higher salinity ore fluids in sulfur reducing conditions. In contrast, the massive sulfide ores from the Federal Flag deposit contain Fe‐rich sphalerite and subordinate sulfarsenides. Native gold blebs occur as inclusions in Fe‐rich sphalerite, along sphalerite grain boundaries, and in the siliceous‐hematitic matrix. Such occurrences of native gold suggest that gold was initially precipitated from high‐temperature, moderate to highly reduced, low‐sulfur ore fluids. Concentrations of Au and Ag from both Laloki and Federal Flag deposits were within the range (<10 ppm Au and <100 ppm Ag) of massive sulfides at a mid‐ocean ridge setting rather than typical arc‐type massive sulfides. The complex relationship between FeS contents in sphalerite and gold grades of both deposits is probably due to the initial deposition of gold on the seafloor that may have been controlled by factors such as Au complexes, pH, and fO₂ in combination with temperature and sulfur fugacity.     

Origin and evolution of hydrothermal fluids in the Taochong iron deposit,Middle–Lower Yangtze Valley,Eastern China: Evidence from microthermometric and stable isotope analyses of fluid inclusions

The Middle–Lower Yangtze River Valley is one of the most important metallogenic belts in China, hosting numerous Cu–Fe–Au–Mo deposits. The Taochong deposit is located in the northern part of the Fanchang iron ore district of the Middle–Lower Yangtze River metallogenic belt. The Fe-orebody is hosted by Middle Carboniferous to Lower Permian limestones. Skarns and Fe-orebodies occur as tabular bodies along interlayer-gliding faults, at some distance from the inferred granitic intrusions. Field evidence and petrographic observations indicate that the three stages of hydrothermal activity—the skarn, iron oxide (main mineralization stage), and carbonate stages—all contributed to the formation of the Taochong iron deposit. The skarn stage is characterized by the formation of garnet and pyroxene, with high-temperature, hypersaline hydrothermal fluids with isotopic compositions similar to those of typical magmatic fluids. These fluids were probably generated by the separation of brine from a silicate melt instead of the product of aqueous fluid immiscibility. The iron oxide stage coincides with the replacement of garnet and pyroxene by actinolite, chlorite, quartz, calcite and hematite. The hydrothermal fluids at this stage are represented by saline fluid inclusions that coexist with vapor-rich inclusions with anomalously low δD values (− 66‰ to − 94‰). The decrease in ore fluid δ¹⁸O_water with time and decreasing depth is consistent with the decreases in fluid salinity and temperature. The fluid δD values also show a decreasing trend with decreasing depth. Both fluid inclusion and stable isotopic data suggest that the ore fluid during the main period of mineralization was evolved by the boiling of various mixtures of magmatic brine and meteoric water. This process was probably induced by a drop in pressure from lithostatic to hydrostatic. The carbonate stage is represented by calcite veins that cut across the skarn and orebody, locally producing a dense stockwork. This observation indicates the veins formed during the waning stages of hydrothermal activity. The fluids from this stage are mainly represented by a variety of low-salinity fluid inclusions, as well as fewer high-salinity inclusions. These particular fluids have the lowest δ¹⁸O_water values (− 2.2‰ to 0.4‰) and a wide of range of δD values (− 40‰ to − 81‰), which indicate that they were originated from a mixture of residual fluids from the oxide stage, various amounts of meteoric water, and possibly condensed vapor. Low-temperature boiling probably occurred during this stage.We also discuss the reasons behind the anomalously low δD values in fluid inclusion water extracted by thermal decrepitation from quartz at high temperatures, and suggest that calcite data provide a possible benchmark for adjusting low δD values found in quartz intergrown with calcite.     

Fluid evolution,wallrock alteration,and ore mineralization associated with the Rodalquilar epithermal gold-deposit in southeast Spain

At Rodalquilar gold mineralization is found in Late Tertiary volcanic rocks of the Sierra del Cabo de Gata and is related to a caldera collapse. Radial and concentric faults were preferred sites for gold deposition. Hydrothermal activity produced a specific alteration zoning around gold-bearing vein structures, grading from an innermost advanced argillic via an argillic into a more regionally developed propylitic zone. Advanced argillic alteration with silica, pyrophyllite, alunite, and kaolinite extends down to several hundred m indicating a hypogene origin. High-grade gold mineralization in vein structures is confined to the near-surface part of the advanced argillic alteration. Fine-grained gold is associated with hematite, jarosite, limonite, or silica. At a depth of about 120 m, the oxidic ore assemblage grades into sulfide mineralization with pyrite and minor chalcopyrite, covellite, bornite, enargite, and tennantite. Two types of fluids from different sources were involved in the hydrothermal system. Overpressured and hypersaline fluids of presumably magmatic origin initiated the hydrothermal system. Subsequent hydrothermal processes were characterized by the influx of low-salinity solutions of probable marine origin and by interactions between both fluids. Deep-reaching, advanced argillic alteration formed from high-salinity fluids with 20–30 equiv. wt% NaCl at about 225°C. Near-surface gold precipitation and silification are related to fluids with temperatures of about 175°C and 3–4 equiv. wt% NaCl. Gold was transported as Au(HS) ₂ ^– , and precipitation resulted from boiling with a concomitant decrease in temperature, pressure, and pH and an increase in fO₂. All features of the Rodalquilar gold deposit reveal a close relationship to acid-sulfate-type epithermal gold mineralization.     

大型斑岩铜矿成矿的深部构造岩浆活动背景

笔者以深部地球物理探测结果为基础，将地球物理与地质、地球化学资料结合起来分析了南美稳态的洋陆俯冲体制下安第斯斑岩铜矿带、藏南不稳态的陆陆碰撞体制下冈底斯斑岩铜矿带和不稳态的陆岛陆碰撞体制下三江地区的玉龙斑岩铜矿带渐新世以来深部成矿的构造岩浆活动背景条件，总结归纳出6条成矿的基本条件：（1）要有上地幔来源的高温岩浆热液的大量供给；（2）要有区域性铜的萃取来源；（3）要有上地壳的部分熔融层或岩浆房。以提供含铜热液的循环沉淀条件；（4）地壳上层构造体系中的张性断裂。以供岩浆热液的就位；（5）围岩的化学性质对矿质沉淀是重要的；（6）构造的相对稳态期。为矿质大量沉淀积累创造条件。在不稳态体制下要寻找相对稳态的时段。陆陆碰撞体制与洋陆俯冲体制下成矿作用的主要不同之处是构造的不稳态期长、陆壳加厚与构造复杂化．岩石层碎裂发育机制等。提出了冈底斯带的新的找矿远景地带。     

Numerical Simulation of Fluid Migration during Ore Formation of Carboniferous Exhalation-Sedimentary Massive Sulfide Deposits in the Tongling District, Anhui Province

Numerical simulation of fluid migration during the ore-forming process of the Carboniferous exhalationsedimentary (Sedex) massive sulfide deposits in the Tongling district shows that fluid and thermal activities in lying-wall rocks were limited to a small area around the main draining passage, which led to weak mineralization and alteration in the lying-wall rock. Temperature and fluid fields indicate that mineralization and alteration in the lying-wall rock of the Sedex-type deposits are usually weaker than those of volcano-hosted massive sulfide deposits. Fluid migration involves the following processes: seawater penetrating and leaching the lying-wall rocks, then mixing with ascending hydrothermal fluids in the main draining passage, and finally jetting into seafloor. Although fluid activity-influenced area is rather small,the content of metals leached out from the lying-wall rocks is high enough to form large-scale ore deposits. Tensional contemporaneous faults accompanied with strong heat flows controlled the formation and distribution of Sedex deposits.The tensional tectonic regime on the northern margin of the Yangtze block during the Hercynian provided Sedex deposits with a prerequisite geodynamic condition.     

The mineral chemistry of hydrothermally altered and metamorphosed wall-rocks at the Stollberg Fe-Pb-Zn-Mn(-Ag) deposit,Bergslagen, Sweden

The c. 1.9 Ga old Stollberg sulphide and Mnrich skarn iron ores and sulphide ores in Bergslagen, south-central Sweden are hosted by hydrothermally altered and metamorphosed felsic volcanic and volcaniclastic rocks. The ores are underlain by comformable alteration zones characterized by albite-gedrite-quartz and biotite-muscovite-plagioclase-K-feldspar-quartz +/– garnet assemblages. The present mineralogies are interpreted as medium-grade metamorphic equivalents to the original alteration mineral assemblages. PT-conditions during prograde regional metamorphism are semiquantatively determined to be 510 to 560 °C at approximately 3 kbar. With increasing modal content of gedrite and biotite in the alteration zones, the Mg/Fe ratios and X_Mg's in octahedral positions of these minerals also increase. In the gedrite-bearing strata, whole-rock Mg/Fe ratios remain constant, whereas in the biotite-rich unit the wholerock Mg/Fe trend is parallel to that of the biotites.The trends in the metamorphic mineral composition are interpreted to be a product of original changes in fluid composition during the evolution of a sub-seafloor hydrothermal system. During the initial stage of alteration, Fe-Mn-rich fluids altered the rocks, and during a later stage, the fluids became more Mg-rich, possibly due to entrainment of fresh seawater, and the alteration zones became relatively more Mg-rich. Sulphide precipitation was contemperaneous with Mg metasomatism, suggesting base metal precipitation was a function of the mixing of cool seawater with hydrothermal fluid. It is proposed that early hydrothermal alteration was associated with the deposition of areally extensive Fe-oxide formation, and that Mg metasomatism defines a second stage of hydrothermal activity during which sulphide mineralization overprinted the earlier formed Fe-oxide deposit.     

Iron isotope fractionation during hydrothermal ore deposition and alteration

Iron isotopes fractionate during hydrothermal processes. Therefore, the Fe isotope composition of ore-forming minerals characterizes either iron sources or fluid histories. The former potentially serves to distinguish between sedimentary, magmatic or metamorphic iron sources, and the latter allows the reconstruction of precipitation and redox processes. These processes take place during ore formation or alteration. The aim of this contribution is to investigate the suitability of this new isotope method as a probe of ore-related processes. For this purpose 51 samples of iron ores and iron mineral separates from the Schwarzwald region, southwest Germany, were analyzed for their iron isotope composition using multicollector ICP-MS. Further, the ore-forming and ore-altering processes were quantitatively modeled using reaction path calculations. The Schwarzwald mining district hosts mineralizations that formed discontinuously over almost 300 Ma of hydrothermal activity. Primary hematite, siderite and sulfides formed from mixing of meteoric fluids with deeper crustal brines. Later, these minerals were partly dissolved and oxidized, and secondary hematite, goethite and iron arsenates were precipitated. Two types of alteration products formed: (1) primary and high-temperature secondary Fe minerals formed between 120 and 300 °C, and (2) low-temperature secondary Fe minerals formed under supergene conditions (<100 °C). Measured iron isotope compositions are variable and cover a range in δ⁵⁶Fe between −2.3‰ and +1.3‰. Primary hematite (δ⁵⁶Fe: −0.5‰ to +0.5‰) precipitated by mixing oxidizing surface waters with a hydrothermal fluid that contained moderately light Fe (δ⁵⁶Fe: −0.5‰) leached from the crystalline basement. Occasional input of CO₂-rich waters resulted in precipitation of isotopically light siderite (δ⁵⁶Fe: −1.4 to −0.7‰). The difference between hematite and siderite is compatible with published Fe isotope fractionation factors. The observed range in isotopic compositions can be accounted for by variable fractions of Fe precipitating from the fluid. Therefore, both fluid processes and mass balance can be inferred from Fe isotopes. Supergene weathering of siderite by oxidizing surface waters led to replacement of isotopically light primary siderite by similarly light secondary hematite and goethite, respectively. Because this replacement entails quantitative transfer of iron from precursor mineral to product, no significant isotope fractionation is produced. Hence, Fe isotopes potentially serve to identify precursors in ore alteration products. Goethites from oolitic sedimentary iron ores were also analyzed. Their compositional range appears to indicate oxidative precipitation from relatively uniform Fe dissolved in coastal water. This comprehensive iron isotope study illustrates the potential of the new technique in deciphering ore formation and alteration processes. Isotope ratios are strongly dependent on and highly characteristic of fluid and precipitation histories. Therefore, they are less suitable to provide information on Fe sources. However, it will be possible to unravel the physico-chemical processes leading to the formation, dissolution and redeposition of ores in great detail.     

Microthermometry and geochemistry of fluid inclusions from the Tennant Creek gold-copper deposits: implications for ore deposition and exploration

Gold-copper-bismuth mineralization in the Tennant Creek goldfield of the Northern Territory occurs in pipe-like, ellipsoidal, or lensoidal lodes of magnetite ± hematite ironstones which are hosted in turbiditic sedimentary rocks of Proterozoic age. Fluid inclusion studies have revealed four major inclusion types in quartz associated with mineralized and barren ironstones at Ten nant Creek; (1) liquid-vapour inclusions with low liquid/vapour ratios (Type I), (2) liquid-vapour inclusions with high liquid/vapour ratios or high vapour/liquid ratios and characteristic dark bubbles (Type II), (3) liquid-vapour-halite inclusions (Type III), and (4) liquid-vapour inclusions with variable liquid/vapour ratios (Type V). Type I inclusions are present in the barren ironstones and the unmineralized portions of fertile ironstones, whereas Types II and III inclusions are recognized in fertile ironstones. Trails of Types II and III inclusions cut trails of Type I inclusions. Type I fluid inclusions have homogenization temperatures of 100° to 350 °C with a mode at 200° to 250 °C. Type II inclusions in mineralized ironstones (e.g. Juno, White Devil, Eldorado, TC8 and Gecko K-44 deposits) have homogenization temperatures of 250 °C to 600 °C with a mode of 350 °C. Type I fluid inclusions have a salinity range of 10 to 30 NaCl equiv. wt %. Salinity measurements on fluid inclusions in the mineralized zones gave a range of 10 to 50 NaCl equiv. wt % with a mode of 35 NaCl equiv. wt %. Fluid inclusion studies indicate that the Tennant Creek ironstones were formed from a relatively low temperature and moderately saline fluid, where as gold and copper mineralization was deposited from later hydrothermal fluids of higher temperature and salin ity. Gas analysis indicates the presence of N₂ and CO₂, with very minor CH₄ in Types II inclusions but no N₂ or CH₄ gases in Type I inclusions. Microprobe analysis of the fluid inclusion decrepitates indicates that the inclusions from Tennant Creek contain sodium and calcium as dominant cations and potassium in a subordinate amount. The high temperatures ( 350 °C), high salinities ( 35 NaCl equiv. wt. %) and cation composition of the Tennant Creek ore fluids suggest that the ore fluids were derived from upward migrating heated basinal brines, although contribution from a magmatic source cannot be ruled out. Close association of vapour-rich Type IIb and salt-rich Type III inclusions in the mineralized ironstones (e.g. Juno, White Devil, Eldorado, TC8 and Gecko K-44) indicates heterogeneous trapping of ore fluids. This heterogeneous trapping is interpreted to be due to unmixing (exsolution) of a gas-rich (e.g. N₂) fluid during the upward migration of the metal bearing brines and/or due to degassing caused by reaction of oxidized ore fluids and host ironstones. Fluid inclusion data have important implications regarding the deposition of gold in the ironstones, and may have application in discriminating fertile from barren ironstones.     

Hydrothermal alteration,fluid inclusions and stable isotope systematics of the Alvo 118 iron oxide–copper–gold deposit,Carajás Mineral Province (Brazil): Implications for ore genesis

The Alvo 118 iron oxide–copper–gold (IOCG) deposit (170 Mt at 1.0 wt.% Cu, 0.3 g/t Au) lies in the southern sector of the Itacaúnas Shear Belt, Carajás Mineral Province, along a WNW–ESE-striking, 60-km-long shear zone, close to the contact of the ~2.76-Ga metavolcano-sedimentary Itacaiúnas Supergroup and the basement (~3.0 Ga Xingu Complex). The Alvo 118 deposit is hosted by mafic and felsic metavolcanic rocks and crosscutting granitoid and gabbro intrusions that have been subjected to the following hydrothermal alteration sequence towards the ore zones: (1) poorly developed sodic alteration (albite and scapolite); (2) potassic alteration (biotite or K-feldspar) accompanied by magnetite formation and silicification; (3) widespread, pervasive chlorite alteration spatially associated with quartz–carbonate–sulphide infill ore breccia and vein stockworks; and (4) local post-ore quartz–sericite alteration. The ore assemblage is dominated by chalcopyrite (~60%), bornite (~10%), hematite (~20%), magnetite (10%) and subordinate chalcocite, native gold, Au–Ag tellurides, galena, cassiterite, F-rich apatite, xenotime, monazite, britholite-(Y) and a gadolinite-group mineral. Fluid inclusion studies in quartz point to a fluid regime composed of two distinct fluid types that may have probably coexisted within the timeframe of the Cu–Au mineralizing episode: a hot (>200°C) saline (32.8‰ to 40.6 wt.% NaCl eq.) solution, represented by salt-bearing aqueous inclusions, and a lower temperature (<200°C), low to intermediate salinity (<15 wt.% NaCl eq.) aqueous fluid defined by two-phase (L_H2O + V_H2O) fluid inclusions. This trend is very similar to those defined for other IOCG systems of the Carajás Mineral Province. δ ¹⁸O_H2O values in equilibrium with calcite (−1.0‰ to 7.5‰ at 277°C to 344°C) overlap the lower range for primary magmatic waters, but the more ¹⁸O-depleted values also point to the involvement of externally derived fluids, possibly of meteoric origin. Furthermore, sulphide δ ³⁴S values (5.1‰ to 6.3‰), together with available boron isotope and Cl/Br–Na/Cl data provide evidence for a significant component of residual evaporative fluids (e.g., bittern fluids generated by seawater evaporation) in this scenario that, together with magma-derived brines, would be the main sources of the highly saline fluids involved in the formation Alvo 118 IOCG deposit. The restricted high temperature sodic alteration, the pervasive overprinting of the potassic alteration minerals by chlorite proximal to the ore zones, ore breccias with open-space filling textures in brittle structures, microthermometric and stable isotope data indicate, collectively, that the Alvo 118 IOCG system developed at structurally high levels and may be considered the shallower representative of the IOCG systems of the CMP.     

熊耳山—外方山矿集区中生代Au-Mo成矿系统

熊耳山—外方山矿集区位于秦岭造山带之华北板块南缘,经历了复杂的碰撞造山过程,成矿时间跨度大,成矿强度高,成矿作用多样。复合造山过程和相应的成矿作用已被深入研究,但成矿系统的划分和叠加成矿作用尚需研究。本文将熊耳山—外方山矿集区发育的Au-Mo矿床划分为造山型Mo矿床、斑岩型Mo矿床、岩浆热液脉型Mo矿床、造山型Au矿床和岩浆热液型Au矿床5个类型,对应5种成矿系统：(1)造山型Mo矿床形成于250~227 Ma的同碰撞环境和227~194 Ma的后碰撞环境,为变质热液萃取壳源Mo成矿;(2)斑岩型Mo矿床形成于163~135 Ma的洋陆俯冲环境和135~116 Ma的岩石圈减薄环境,为岩浆热液携带幔源或壳源Mo成矿;(3)岩浆热液脉型Mo矿床形成于227~194 Ma的后碰撞环境,为岩浆热液携带幔源Mo成矿;(4)造山型Au矿床在三叠纪发生了预富集作用,主要形成于163~135 Ma的洋陆俯冲环境和135~103 Ma的岩石圈减薄环境,为变质热液萃取壳源Au成矿;(5)岩浆热液型Au矿床仅形成于135~103 Ma的岩石圈减薄环境,为岩浆热液携带壳源Au成矿。矿集区主要存在两种叠加成矿作用,即不同构造背景下多种成矿系统的叠加和同一构造背景下不同成矿系统的叠加。     

Hydrothermal environments during the genesis of silver deposits in the Northwest Territories of Canada: Evidence from fluid inclusions

The Ag-Ni-Co-Bi-As-U veins in the Northwest Territories of Canada are hosted by volcano-sedimentary and intrusive rocks of the Great Bear Batholithic Complex. Fluid inclusion data from the gangue minerals of the veins suggest a wide range in salinity and temperature for the hydrothermal fluids. The salinities of the fluids range from about 15 to 35 wt.% NaCl equivalent. The homogenization temperatures range from 150° to 250°C for stage I fluids; 220° to 480°C for stage II fluids; 250° to 350°C for stage III fluids; 150° to 250°C for stage IV fluids and 90° to 250°C for stage V fluids. The coexistence of liquid-rich and vapour-rich inclusions in stages II and III minerals suggest that the hydrothermal fluids were boiling or effervescing. The coexistence of saturated and unsaturated inclusions in stages II and III minerals may be due to effervescence of a less saline fluid, whilst for stages IV and V it may be due to mixing of a highly saline fluid with a less saline fluid, or due to alternation of hydrostatic and lithostatic pressures at the time of trapping of the inclusions.     

Multi-isotope approach for the identification of metal and fluid sources of the Arroyo Rojo VMS deposit,Tierra del Fuego,Argentina

The Arroyo Rojo deposit, located in Tierra del Fuego, is the most important polymetallic, volcanic-hosted massive sulphide in the rhyolitic belt of the Fuegian Andes. The best intercepts in drill holes indicate a true thickness of 18.6 m and concentrations of 2.2% Cu, 3.9% Pb, 14.5% Zn, 140 g/t Ag, 1.1 g/t Au). This deposit, located near the town of Ushuaia, is hosted in a Middle Jurassic volcanic and volcanoclastic sequence. Massive and semimassive bodies display stacked lenticular morphologies with disseminated mineralization in both the footwall and hanging wall. The associated hydrothermal alteration system is partially conformable with the layering of the volcanic rocks. The ores and host rocks display a penetrative tectonic foliation and were metamorphosed to greenschist facies.Previous studies have not resulted in a consensus regarding the nature and the source of ore-forming fluids and the style of deposition of the sulphides at Arroyo Rojo. In this study, both stable and radiogenic isotopes were used develop a better understanding of these aspects of the deposit.Hydrogen and oxygen isotopes indicate that an evolved seawater mixed with significant contributions from other fluid reservoirs such as magmatic and/or metamorphic waters was the most likely source of the ore-forming fluids. These fluids underwent significant interaction with the underlying volcanic and sedimentary rocks, which promoted partial (Sr isotopes) or full (Pb isotopes) homogenization of radiogenic isotopes. δ³⁴S_CDT values suggest that the sulphur was derived from several sources: biogenic reduction of seawater sulphate (BSR) in a restricted to closed basin was mixed with a heavier component derived from inorganic reduction of seawater sulphate (TRS) and possibly from sulphur leached from igneous footwall rocks and/or direct contribution from magmatic fluids.Lateral infiltration of hydrothermal fluids resulted in the formation of a halo of semimassive to disseminated ore due to the replacement of porous, reactive glassy and breccia tuffs.As a result of the hydrothermal circulation, two styles of mineralization are observed in the Arroyo Rojo deposit: a stringer zone and a halo of semimassive to disseminated ore corresponding to sub-seafloor replacement, and syn-sedimentary mineralization consisting of massive sulphides.This model is consistent with the geodynamic context of the study area: a narrow, deep-marine volcano-tectonic rift parallel to the Andean side of South America and related to the initial break-up of Gondwana (ca. 145 Ma).     

河南西峡石板沟金矿成矿流体地球化学及矿床成因讨论

石板沟金矿是近年在豫西南发现的一个剪切带容矿的脉状金矿。根据流体包裹体地球化学研究,分析了矿床成矿流体地球化学特征,讨论了金的沉淀机制和矿床成因。构造蚀变岩型金矿的形成主要与热液蚀变作用有关,石英脉型金矿的形成,则可能主要与岩浆热液与变质热液的混合作用有关。矿质主要源自晋宁期岩浆岩,成矿流体和热能主要来自海西期花岗岩。矿床为剪切带容矿的中低温热液金矿床。