Textural and fluid inclusion constraints on the origin of the banded-iron-formation-hosted gold deposits at Maevatanana,central Madagascar

The Maevatanana deposits consist of gold-bearing quartz–sulphide veins crosscutting banded iron formation (BIF) within a metamorphosed 2.5 Ga greenstone belt. The host rocks are dominated by a sequence of migmatites, gneisses, amphibolites, magnetite-rich quartzites and soapstones, intruded by large granitoid batholiths (e.g. the 0.8 Ga Beanana granodiorite). In the mineralised rocks, pyrite is the dominant sulphide, in addition to accessory chalcopyrite and galena. Outside the immediate ore zone, the BIF is dominated by quartz + magnetite ± hematite, accompanied by cummingtonite, albite and biotite. Gold occurs as globular grains (usually <500 μm) within quartz crystals close to the sulphides and as invisible inclusions within pyrite and chalcopyrite (up to 2,500 ppm Au content). Fluid inclusion textural and microthermometric studies indicate heterogeneous trapping of a low-salinity (∼3.6 wt.% eq. NaCl) aqueous fluid coexisting with a carbonic fluid. Evidence for fluid-phase immiscibility during ore formation includes variable L/V ratios in the inclusions and the fact that inclusions containing different phase proportions occur in the same area, growth zone, or plane. Laser Raman spectroscopy confirms that the vapour phase in these inclusions is dominated by CO₂ but shows that it may contain small amounts of CH₄ (<1 mol%), H₂S (<0.05 mol%) and traces of N₂. Fluid inclusion trapping conditions ranged from 220 to 380°C and averaged 250°C. Pressure was on the order of 1–2 kbar. The abundant CO₂ and low salinity of the inclusions suggest a metamorphic origin for the fluid. Likewise, the presence of H₂S in the fluid and pyritisation of the wall-rock indicate that gold was likely transported by sulphide complexing. Fluid immiscibility was probably triggered by the pressure released by fracturing of the quartzites during fault movements due to competence differences with the softer greenstones. Fracturing greatly enhanced fluid circulation through the BIF, allowing reaction of the sulphide-bearing fluids with the iron oxides. This caused pyrite deposition and concomitant Au precipitation, enhanced by fluid phase separation as H₂S partitioned preferentially into the carbonic phase.     

Origin and evolution of the calcic and magnesian skarns hosting the El Valle-Boinás copper–gold deposit, Asturias (Spain)

The El Valle-Boinás copper–gold deposit is located in the southern part of the Rio Narcea Gold Belt 65 km west of Oviedo (NW Spain), within the Cantabrian Zone (Iberian Hercynian Massif). The deposit is related to the Boinás stock, which ranges from quartz-monzonite to monzogranite and intruded (303 Ma) the carbonated Láncara Formation (early Cambrian) and the siliciclastic Oville Formation (middle-late Cambrian).A copper–gold skarn was developed along the contact between the igneous rock and the carbonated sedimentary rocks. The skarn distribution and mineralogy reflects both structural and lithologic controls. Two types of skarn exists: a calcic skarn mainly developed in the upper calcic member of the Láncara Formation, and a magnesian skarn developed in the lower dolomitic and organic-rich member. The former mainly consists of garnet, pyroxene and wollastonite. Retrograde alteration consists of K-feldspar, epidote, quartz, calcite, magnetite, ferroactinolite, titanite, apatite, chlorite and sulfides. Magnesian skarn mainly consists of diopside with interbedded forsterite zones. Pyroxene skarn is mainly altered to tremolite, with minor phlogopite and serpentine. Olivine skarn is pervasively altered to serpentine and magnetite, and is commonly accompanied by high sulfide and gold concentrations. This altered skarn results in a very dark rock, referred to as “black skarn”, which has great importance in gold reserves. Sulfide mineralization mainly consists of chalcopyrite, bornite, arsenopyrite, pyrrhotite and pyrite, while wittichenite, sphalerite, digenite, bismuthinite, native bismuth and electrum occur as accessory minerals.After extensive erosion, reactivation of the northeast-trending fracture zone provided conduits for the subsequent emplacement of porphyritic dikes (285±4 Ma) and diabasic dikes (255±5 Ma). Alteration, characterized by sericitization, silicification, carbonatization and hypogene oxidation took place, as did sulfide mineralization (pyrite, arsenopyrite, sphalerite, chalcopyrite, galena, bournonite, and Fe–Pb–Sb sulfosalts). Veins with quartz, carbonate, adularia and sulfide minerals crosscut all previous lithologies. Jasper and jasperoid breccias developed at the upper parts of the deposits.The fluid inclusion and stable isotope studies suggest a predominantly magmatic prograde-skarn fluid characterized by high-salinity (26–28 wt.% KCl and 32–36 wt.% NaCl) and high temperature, above 580°C. This fluid evolved into two immiscible fluids: a CO₂- and/or CH₄-rich, high-salinity aqueous fluid. Temperatures for the first retrograde-stage are between 350 and 425°C. A second stage is related to a more diluted aqueous fluid (3–6.2 wt.% NaCl eq.) and temperatures from 280 to 325°C. The fluid inclusion study performed on quartz from low-temperature mineralization indicates a very low salinity (0.2–6.2 wt.% NaCl eq.), low-temperature aqueous fluid (from 150 to 250°C), and trapping pressure conditions less than 0.2 kbar. In addition, the stable isotope study suggests that an influx of metamorphic waters derived from the country rocks produced these lower temperature fluids. The last control for the Au mineralization is the Alpine tectonism, which developed fault breccias (cataclasites to, locally, protomylonites) and gold remobilization from previous mineralization.     

Nature and source of the ore-forming fluids associated with orogenic gold deposits in the Dharwar Craton

Neoarchean orogenic gold deposits, associated with the greenstone-granite milieus in the Dharwar Craton include(1) the famous Kolar mine and the world class Hutti deposit;(2) small mines at HiraBuddini, Uti, Ajjanahalli, and Guddadarangavanahalli;(3) prospects at Jonnagiri; and(4) old mining camps in the Gadag and Ramagiri-Penakacherla belts. The existing diametric views on the source of ore fluid for formation of these deposits include fluids exsolved from granitic melts and extracted by metamorphic devolatilization of the greenstone sequences. Lode gold mineralization occurs in structurally controlled higher order splays in variety of host rocks such as mafic/felsic greenstones, banded iron formations, volcaniclastic rocks and granitoids. Estimated metamorphic conditions of the greenstones vary from lower greenschist facies to mid-amphibolite facies and mineralizations in all the camps are associated with distinct hydrothermal alterations. Fluid inclusion microthermometric and Raman spectroscopic studies document low salinity aqueous-gaseous(H_2O + CO_2 ± CH_4 + NaCl) ore fluids,which precipitated gold and altered the host rocks in a narrow P-T window of 0.7-2.5 kbar and 215-320℃. While the calculated fluid O-and C-isotopic values are ambiguous, S-isotopic compositions of pyrite-precipitating fluid show distinct craton-scale uniformity in terms of its reduced nature and a suggested crustal sulfur source.Available ages on greenstone metamorphism, granitoid plutonism and mineralization in the Hutti Belt are tantamount, making a geochronology-based resolution of the existing debate on the metamorphic vs.magmatic fluid source impossible. In contrast, tourmaline geochemistry suggests involvement of single fluid in formation of gold mineralization, primarily derived by metamorphic devolatilization of mafic greenstones and interlayered sedimentary rocks, with minor magmatic contributions. Similarly, compositions of scheelite, pyrite and arsenopyrite point toward operation of fault-valves that caused pressure fluctuation-induced fluid phase separation, which acted as the dominant process of gold precipitation,apart from fluid-rock sulfidation reactions. Therefore, results from geochemistry of hydrothermal minerals and those from fluid inclusion microthermometry corroborate in constraining source of ore fluid,nature of gold transport(by Au-bisulfide complex) and mechanism of gold ore formation in the Dharwar Craton.     

Genesis and mineralization of gold-bearing quartz veins in the Xiao Qinling area, central China

Gold-bearing quartz veins of the Taihua Group consisting of Archean metavolcanic rocks are a main gold deposit type in the Xiao Qinling area,one of the three biggest gold production areas in China.The quartz veins experienced strong alteration characterized by a typical mesothermal hydrothermal altered mineral assemblage.The grade of gold is affected by the contents of sulphides,e.g.galena,pyrite and chalcopyrite.Results of minor elements analysis for the of gold-bearing quartz veins indicate higher contents of Au and high contents of Ag,Pb,Cu,Cd,W,and Mo.Abundant fluid inclusions were found in the gold-bearing quartz veins.Three types of fluid inclusions were identified:(1) aqueous inclusions;(2) CO 2-bearing inclusions;and(3) daughter crystal-bearing fluid inclusions.Homogenization temperatures ranged from 110 to 670℃ with low and high peaks appearing at 160 180℃ and 280 300℃,respectively.The salinity of aqueous inclusions varies between 1.8 wt% and 38.2 wt% NaCl.The homogenization temperature and salinity show a positive correlation.The H and O isotopes of fluid inclusions in the gold-bearing quartz veins indicate that magmatic solution and metamorphic hydrothermal solution,together with meteoric water,were involved in the formation of gold-bearing fluid.Mesozoic magma activities related to granite intrusions should be the main source of CO 2 fluid with higher temperature and salinity.     

Gold and copper mineralization at the El Indio deposit, Chile

A Middle Tertiary volcanic belt in the High Andes of north-central Chile hosts numerous precious- and base-metal epithermal deposits over its 150 km north-south trend. The El Indio district, believed to be associated with a hydrothermal system in the late stages of development of a volcanic caldera, consists of a series of separate vein systems located in an area of 30 km² which has undergone intense argillic-sericitic-solfataric alteration. The majority of the known gold-copper-silver mineralization occurs within a structural block only 150 by 500 m in surface area, with a recognized vertical extent exceeding 300 m. This block is bounded by two high-angle northeast-trending faults oriented subparallel to the mineralized veins.Hypogene mineralization at El Indio is grouped into two main ore-forming stages: Copper and Gold. The Copper stage is composed chiefly of enargite and pyrite forming massive veins up to 20 m wide, and is accompanied by alteration of the wall rocks to alunite, kaolinite, sericite, pyrite and quartz. The Gold stage consists of vein-filling quartz, pyrite, native gold, tennantite and subordinate amounts of a wide variety of telluride minerals. Associated with this stage is pervasive alteration of the wall rocks to sericite, kaolinite, quartz and minor pyrophyllite. The transition from copper to gold mineralization is marked by the alteration of enargite to tennantite and by minor deposition of sphalerite, galena, huebnerite, chalcopyrite and gold. Mineral stability relations indicate that there was a general decrease in the activity of S₂ accompanied by variations in the activity of Te₂ during the Gold stage.Fluid-inclusion data show homogenization temperatures ranging from about 220 to 280°C, with salinities on the order of 3–4 eq. wt. % NaCl for the Copper stage. The Gold-stage inclusions indicate a similar range in homogenization temperatures, but significantly lower salinities (0.1–1.4 eq. wt. % NaCl). Fluid inclusions of transition minerals show a weak inverse relationship between homogenization temperatures (190–250°C) and salinities (3.4–1.4 eq. wt. % NaCl), which may represent mixing of hotter Gold-stage fluids with cooler late-Copper-stage fluids. No evidence of boiling was found in fluid inclusions, but CO₂ vapor-rich inclusions were identified in wall-rock quartz phenocrysts which pre-date copper and gold mineralization.Mineral stability calculations indicate that given a fairly restricted range of solution compositions, the Copper-, Transition- and Gold-stage minerals at El Indio could have been deposited from a single solution, with constant total dissolved sulfur which underwent reduction through time. Limited sulfur-isotope data indicates that pyrite from the Copper stage was not in isotopic equilibrium with Copper-stage alunite or Transition-stage sphalerite. The sulfur-isotope and fluid-inclusion data indicate that two fluids with comparable temperatures but different compositions flowed through the El Indio system. The earlier fluid deposited copper attended by sericite-alunite-kaolinite alteration, and later epithermal fluids deposited gold with quartz-sericite-kaolinite-pyrite alteration.     

The New Consort Gold Mine,Barberton greenstone belt,South Africa: orogenic gold mineralization in a condensed metamorphic profile

The New Consort Gold Mine in the Palaeo- to Mesoarchaean Barberton greenstone belt, South Africa is one of the oldest recognized orogenic gold deposits on Earth. The gold mineralization is hosted by discrete mylonitic units that occur at, or close to, the contact between the mafic and ultramafic volcanic rocks of the c. 3,280 Ma Onverwacht Group and the mainly metasedimentary rocks of the overlying c. 3,260–3,230 Ma Fig Tree Group. This contact, locally referred to as the Consort Bar, formed during ductile D₁ imbrication of the metavolcanosedimentary sequence and predates the main stage of the gold mineralization. The imbricate stack is situated in the immediate hanging wall of the basal granitoid–greenstone contact along the northern margin of the greenstone belt. It is characterized by a condensed metamorphic profile in which the metamorphic grade increases from upper greenschist facies conditions (510–530°C, 4 kbar) in rocks of the Fig Tree Group to upper amphibolite facies grades (600–700°C, 6–8 kbar) in the basal Onverwacht Group. Detailed structural and petrological investigations indicate that the Consort Bar represents a major structural break, which is largely responsible for the telescoping of metamorphic isograds within the structural sequence. Two stages of mineralization can be distinguished. Loellingite, pyrrhotite, and a calc–silicate alteration assemblage characterize an early high-T mineralization event, which is restricted to upper amphibolite facies rocks of the Onverwacht Group. This early mineralization may correlate with the local D₁ deformation. The second and main stage of gold mineralization was associated with renewed ductile shearing during D₂. The D₂ deformation resulted in the reactivation of earlier structures, and the formation of a NNW trending, steeply dipping shear zone system, the Shires Shear Zone, which separates two regional SE plunging D₁ synclines. The mineralized shear zones are intruded by abundant syn-kinematic pegmatite dykes that have previously been dated at c. 3040 Ma. Petrological and geothermobarometric data on ore and alteration assemblages indicate that the main stage of gold mineralization, which affected a crustal profile of ca. 1.5 km, was characterized by increasing temperatures (c. 520 to 600°C) with increasing structural depth. Sulfide assemblages in the ore bodies change progressively with metamorphic grade, ranging from arsenopyrite + pyrite + pyrrhotite in the structurally highest to arsenopyrite + pyrrhotite + chalcopyrite + loellingite in the structurally deepest part of the mine. The main stage of gold mineralization was broadly syn-peak metamorphic with respect to the Fig Tree Group, but postdates the peak of metamorphism in upper amphibolite facies rocks of the structurally underlying Onverwacht Group. This indicates that the mineralization coincided with the juxtaposition of the two units. As the footwall rocks were already on their retrograde path, metamorphic devolatilisation reactions within the greenstone sequence can be ruled out as the source of the mineralizing fluids.     

Gold mineralisation at the Lady Bountiful Mine,Western Australia: An example of a granitoid-hosted Archaean lode gold deposit

The Lady Bountiful granitoid-hosted lode gold deposit, located in the mid-greenschist facies metamorphosed Ora Banda greenstone sequence, is hosted predominantly by the late-tectonic Liberty Granodiorite. Gold mineralisation is localised along quartz-veined, sinistral, brittle fault-zone(s) that transect the boundary between the Liberty Granodiorite and Mt Pleasant sill. Quartz vein textures indicate two stages of a single gold-related vein-development event, with high-grade gold mineralisation restricted to the second stage. Ore minerals include pyrite, chalcopyrite, pyrrhotite, galena, sphalerite, Au−Ag−Bi−Pb-tellurides, and native gold. Fluid infitration has resulted in narrow (<1 m) bleached wallrock alteration envelopes to the fault zones comprising albite-K-mica ±chlorite±calcite±rutile assemblages. Temperature-pressure conditions varied from Stage I (300°±50°C, ≈2 kbar) to Stage II (250°±50°C, ≈0.5 to 2 kbar), with the hydrothermal fluid in both stages characterised by X(CO₂)≤0.15 and moderate salinity (≈1.28 m NaCl). Intermittent phase separation of Stage II mineralising fluids, initiated by pressure fluctuations in dilational sites, and/or fluid-dominated fluid: wallrock interaction, are invoked as the dominant depositional mechanisms. The granitoid-hosted Lady Bountiful lode gold deposit shares many features with other granitoid-hosted lode gold deposits in the Yilgarn Craton and the Superior Province. Granitoid-hosted lode gold deposits, such as the Lady Bountiful deposit, provide additional evidence that the dominant control on the localisation of gold mineralisation within a granitoid host is structure, with competency contrasts playing a significant role. Furthermore, the hydrothermal wallrock alteraction and orefluid chemistry characteristics of the granitoid-hosted lode gold deposits are comparable to those established for greenstone-hosted lode gold mineralisation.     

Fluid-magmatic interactions at oceanic islands as a possible source for the sodic agpaitic Trend

Experiments on spilite melting at P = 3 kbar and T = 950−850°C indicate that partial melting in the presence of aqueous fluid (P_{H2 O}P_{H_2 O} = 3 kbar) produces a series of melts of normal alkalinity with up to 77 wt % SiO₂. The partial melts derived from spilite in the presence of aqueous fluid generated in the system NaCl-CaCO₃-H₂O have an agpaitic coefficient increasing to a level sufficient for the origin of alkaline granite in the course of fractional crystallization. An increase in the alkalinity of the melt is explained by soda synthesis in the fluid due to an exchange reaction between CaCO₃ and NaCl. In contrast to NaCl, soda in highly soluble in aluminosilicate melts. We discovered that partial melting in the presence of a soda-bearing fluid results in BaO concentrating from a level of 0.05 wt % in the original spilite to 1 wt % in the partial melt. Conceivably, magmatism in the environment of oceanic islands can occur under conditions favorable for the synthesis of soda-bearing fluids. CO₂ that carbonizes the mafic rocks is provided by mantle plumes, whereas seawater penetrating to depths greater than those of intermediate chambers serves as a source of NaCl. The activity of a fluid-magmatic system is able to generate subalkaline sodic rocks, such as benmoreite and pantellerite.     

Structural controls,temperature–pressure conditions and fluid evolution of orogenic gold mineralisation at the Betam mine,south Eastern Desert,Egypt

The Betam gold deposit, located in the southern Eastern Desert of Egypt, is related to a series of milky quartz veins along a NNW-trending shear zone, cutting through pelitic metasedimentary rocks and small masses of pink granite. This shear zone, along with a system of discrete shear and fault zones, was developed late in the deformation history of the area. Although slightly sheared and boudinaged within the shear zone, the auriferous quartz veins are characterised by irregular walls with a steeply plunging ridge-in-groove lineation. Shear geometry of rootless intra-folial folds and asymmetrical strain shadows around the quartz lenses suggests that vein emplacement took place under a brittle–ductile shear regime, clearly post-dating the amphibolite-facies regional metamorphism. Hydrothermal alteration is pervasive in the wallrock metapelites and granite including sericitisation, silicification, sulphidisation and minor carbonatisation. Ore mineralogy includes pyrite, arsenopyrite and subordinate galena, chalcopyrite, pyrrhotite and gold. Gold occurs in the quartz veins and adjacent wallrocks as inclusions in pyrite and arsenopyrite, blebs and globules associated with galena, fracture fillings in deformed arsenopyrite or as thin, wire-like rims within or around rhythmic goethite. Presence of refractory gold in arsenopyrite and pyrite is inferred from microprobe analyses. Clustered and intra-granular trail-bound aqueous–carbonic (L_CO2 + L_aq ± V_CO2) inclusions are common in cores of the less deformed quartz crystals, whereas carbonic (L_CO2 ± V_CO2) and aqueous H₂O–NaCl (L + V) inclusions occur along inter-granular and trans-granular trails. Clathrate melting temperatures indicate low salinities of the fluid (3–8 wt.% NaCl eq.). Homogenisation temperatures of the aqueous–carbonic inclusions range between 297 and 323°C, slightly higher than those of the intra-granular and inter-granular aqueous inclusions (263–304°C), which are likely formed during grain boundary migration. Homogenisation temperatures of the trans-granular H₂O–NaCl inclusions are much lower (130–221°C), implying different fluids late in the shear zone formation. Fluid densities calculated from aqueous–carbonic inclusions along a single trail are between 0.88 and 0.98 g/cm³, and the resulting isochores suggest trapping pressures of 2–2.6 kbar. Based on the arsenopyrite–pyrite–pyrrhotite cotectic, arsenopyrite (30.4–30.7 wt.% As) associated with gold inclusions indicates a temperature range of 325–344°C. This ore paragenesis constrains f _S2 to the range of 10⁻¹⁰ to 10^−8.5 bar. Under such conditions, gold was likely transported mainly as bisulphide complexes by low salinity aqueous–carbonic fluids and precipitated because of variations in pH and f _O2 through pressure fluctuation and CO₂ effervescence as the ore fluids infiltrated the shear zone, along with precipitation of carbonate and sericite. Wallrock sulphidation also likely contributed to destabilising the gold–bisulphide complexes and precipitating gold in the hydrothermal alteration zone adjacent to the mineralised quartz veins.     

Sources of fluids and material for gold and antimony mineralization in the Adychanskii ore region (East Yakutia,Russia)

The peculiarities of fluid inclusions; the O and C isotope composition of host rocks, vein minerals, and inclusions; and the S and Pb isotope composition of sulfides allowed us to distinguish two groups of fluids with a similar temperature, salinity, and source of the aqueous part produced upon metagenesis and mobilized during collisional events. Quartz-A precipitates from the CO₂–H₂O hydrocarbonate–Na fluid with a salinity of 7–10 wt % eq. NaCl at a depth of ～6 km (290–340°C, 1550 bar). Regeneration of quartz (quartz-C), precipitation of quartz-B, and quartz-AB with carbonate and chlorite occurred at a depth from 3.5 to 1.5 km (250–380°C, 1250–900–350 bar) from CO₂–CH₄–N hydrous sulfate–hydrocarbonate Na–Mg fluids with Cl^–, Ca, and K and a salinity of 5–10 wt % eq. NaCl, and a wide variety of impurities. The localization of veins in sinistral shear dislocations and strong heterogeneity in the P–T conditions allow us to explain the formation of fluid-2 by the postcollisional events.     

Gold potential of the volcanoplutonic zones in the southeastern Siberian Platform and physicochemical conditions of the deposit formation

Numerous gold deposits and occurrences were recognized in the regions of tectonomagmatic activation in the southeastern Siberian Platform. They are located in four metallogenic zones: the Ket-Kap (skarns, quartz veins, and stockworks; gold-bearing lodes in silicitolites; and argillisite-sericite metasomatites), Ulkan (clayey-micaceous metasomatites, quartz veins), Preddzhugdzhur (quartz veins, skarns, and sericite-hydromicaceous metasomatites), and Uda (sericite-hydromicaceous metasomatites). The skarn mineralization is of Meosozoic age, while the mineralization in the quartz veins, quartz-hydromicaceous metasomatites, and quartz-sulfide veins may have a Meosozoic, Paleozoic, or Late Paleozoic age. The highest temperatures were determined for the ore formation in the Preddzhugdzhur skarns (500–715 °C) and the hydrothermal-metasomatic rocks of the Ket-Kap zone (510–530 °C). The composition of gas-liquid inclusions in the minerals of these rocks is dominated by aqueous Na, K, and Ca chloride solutions with salinity up to 40 wt % NaCl equiv; fluid contains CO₂. Quartz veins and stockworks of the Ket-Kap zone were formed under high (up to 465°C) and moderate temperatures and salinity up to 32 wt % NaCl equiv. Sometimes, the minerals in these rocks contain inclusions of low-density CO₂. The gold-bearing veins of the Preddzhugdzhur zone formed at 225–230°C and salinity of 1–2 wt % NaCl equiv. The ore-bearing solutions in the gold-bearing veins of the Ulkan zone are characterized by a potassium-sodium-chlorine composition and salinity of 2–10 wt % NaCl equiv., and the temperature of their formation was 220–280 °C.     

The Aitik Cu–Au–Ag deposit in northern Sweden: a product of high salinity fluids

The Aitik Cu–Au–Ag deposit is located in northern Sweden and is hosted by strongly deformed 1.9 Ga Svecofennian volcano-sedimentary rocks. The main copper mineralization, which occurs as disseminations and veinlets, is hosted by garnet–biotite schist. Subeconomic mineralization in the footwall to the ore is hosted by feldspar–biotite–amphibole gneiss and porphyritic quartz monzodiorite. The deposit has been affected by post-mineralization metamorphic and igneous activity. Fluid inclusions in six samples of copper-mineralized quartz veins record the presence of three different fluid populations. The main ore was deposited from an aqueous, highly saline (31–37 eq. wt% NaCl + CaCl₂) fluid. This fluid was trapped in inclusions intimately associated with the main chalcopyrite mineralization. Later bornite deposition took place from a less saline (18–27 eq. wt% NaCl + CaCl₂), aqueous fluid. A third fluid composed of almost pure CO₂, interacted with the copper-rich system during a post-ore event. The Aitik Cu–Au–Ag deposit shares some features with both porphyry-type and Fe-oxide–Cu–Au deposits. A high calcium content of the ore fluids, similar to other Cu–Au deposits in northern Scandinavia, suggests a contribution to the salinity of the mainly magmatic-hydrothermal fluids from evaporitic rocks in stratigraphically lower units.     

Genesis of the Maanqiao gold deposit in the western Qinling orogen,central China: Constraints from fluid inclusions and in-situ sulfur isotopes

The western Qinling orogen (WQO) is one of the most important prospective gold provinces in China. The Maanqiao gold deposit, located on the southern margin of the Shangdan suture, is a representative gold deposit in the WQO. The Maanqiao deposit is hosted by the metasedimentary rocks of the Upper Devonian Tongyusi Formation. The EW-trending brittle-ductile shear zone controls the orebodies; they occur as disseminated, and auriferous quartz–sulfide vein. The ore-related hydrothermal alteration comprises silicification, sulfidation, sericitization, chloritization, and carbonatization. Native gold is visible and mainly associated with pyrite and pyrrhotite. Mineralization can be classified into the following three stages: bedding-parallel barren quartz–pyrite–(pyrrhotite) (early-stage), auriferous quartz–polymetallic (middle-stage), and carbonate–(quartz)–sulfide (late-stage).Detailed fluid inclusion (FI) studies revealed three types of inclusions in quartz and calcite: aqueous (W-type), CO₂–H₂O (C-type), and pure carbonic (PC-type) FIs. The primary FIs in the early-stage quartz are C- and PC-type, in the middle-stage quartz are mainly W- and C-type, and in the late-stage calcite are only W-type. During gold mineralization, the total FI homogeneous temperatures evolved from 189–375 °C (mostly 260–300 °C) to 132–295 °C (mostly 180–240 °C) to 123–231 °C (mostly 130–150 °C), and the salinities varied among 2.2–9.1 wt.% NaCl equiv. (mostly 5–8 wt.%) to 0.2–9.0 wt.% NaCl equiv. (mostly 3–6 wt.%) to 0.3–3.6 wt.% NaCl equiv. (mostly 2–4 wt.%). The ore-forming fluid was characterized as an H₂O–NaCl−CO₂−CH₄–(N₂) system with medium-low temperature and low salinity. The fluid immiscibility and fluid-rock interaction may be responsible for the precipitation of the sulfides and gold at the Maanqiao gold deposit. Three types of pyrite corresponding to the three mineralization stages, as well as pyrrhotite and arsenopyrite in the middle stage, are micro-analyzed for in-situ sulfur isotopic composition by LA-ICP-MS. Py1 yield near-zero δ³⁴S values of −2.5‰ to 3.0‰, which are somewhat lower than that of the granite hosted pyrites (Py-g, 4.8‰ to 6.6‰). The result suggests a mixed sulfur source from magmatic-hydrothermal fluids and the metamorphism of diagenetic pyrite. Pyrite + pyrrhotite + arsenopyrite assemblages in the middle-stage have relatively higher δ³⁴S values (6.6‰ to 12.3‰) and are mainly developed due to the metamorphism of the ore-host and underlying Devonian sedimentary sequences. The low δ³⁴S values of the late-stage fracture-filled Py3 (−21.9‰ to −17.0‰) resulted from an increasing oxygen fugacity, which was caused by the inflow of oxidized meteoric waters.Based on our studies, the Maanqiao gold deposit is considered to be an orogenic type and closely related to the Indosinian Qinling orogeny.     

Zun-Ospa Gold Deposit,Eastern Sayan: Geology,Ore Composition,and Genesis

The paper discusses the geology of Zun-Ospa gold deposit, which is situated near the Ospino ophiolitic nappe in the southeastern part of the Eastern Sayan, and the ore composition therein. The deposit is related to the tectonic mélange zone and is characterized by distinct structural control. Three consecutive mineral assemblages formed within a temperature range of 380°–170°C: (i) native gold–quartz–pyrite, (ii) gold–quartz–polysulfide, and (iii) silver–sulfosalt. The ore was deposited from low-concentration (5.2–14.2 wt % NaCl equiv.) solutions without CO₂, with the predominance of Mg and Fe chlorides and an admixture of Na and K chlorides. The major ore minerals are pyrite, chalcopyrite, galena, and sphalerite; identified subordinate minerals are pyrrhotite, pentlandite, heazlewoodite, fahlore (tennantite, freibergite), Ni and Ag sulfosalts (ullmannite, miargyrite, polybasite, stephanite), Ag sulfides (mckinstryite, argentite); Au minerals are represented by electrum, kuestelite, and native gold of medium to low fineness. The geological, mineralogical, geochemical, and isotopic characteristics of ore indicate a metamorphic–hydrothermal genesis of mineralization related to the formation of a mélange zone in the duplex strike-slip structure. The sources of ore components are host rock complexes that have been subjected to tectonic deformations, among which rocks of an ophiolitic association predominate, along with fragments of initial hydrothermal–sedimentary ore, granitic, terrigenous, and carbonate rocks. The Late Paleozoic (352 Ma) age of mineralization corresponds to the stage of postcollision shear deformations within the entire Central Asian Foldbelt.     

Genesis of massive sulfide deposits in the Verkhneural’sk ore district, the South Urals, Russia: Evidence for magmatic contribution of metals and fluids

Melt inclusions and aqueous fluid inclusions in quartz phenocrysts from host felsic volcanics, as well as fluid inclusions in minerals of ores and wall rocks were studied at the Cu-Zn massive sulfide deposits in the Verkhneural’sk ore district, the South Urals. The high-temperature (850–1210°C) magmatic melts of volcanic rocks are normal in alkalinity and correspond to rhyolites of the tholeiitic series. The groups of predominant K-Na-type (K₂O/Na₂O = 0.3–1.0), less abundant Na-type (K₂O/Na₂O = 0.15–0.3), and K-type (K₂O/Na₂O = 1.9–9.3) rhyolites are distinguished. The average concentrations (wt %) of volatile components in the melts are as follows: 2.9 H₂O (up to 6.5), 0.13 Cl (up to 0.28), and 0.09 F (up to 0.42). When quartz was crystallizing, the melt was heterogeneous, contained magnetite crystals and sulfide globules (pyrrhotite, pentlandite, chalcopyrite, bornite). High-density aqueous fluid inclusions, which were identified for the first time in quartz phenocrysts from felsic volcanics of the South Urals, provide evidence for real participation of magmatic water in hydrothermal ore formation. The fluids were homogenized at 124–245°C in the liquid phase; the salinity of the aqueous solution is 1.2–6.2 wt % NaCl equiv. The calculated fluid pressure is very high: 7.0–8.7 kbar at 850°C and 5.1–6.8 kbar at 700°C. The LA-ICP-MS analysis of melt and aqueous fluid inclusions in quartz phenocrysts shows a high saturation of primary magmatic fluid and melt with metals. This indicates ore potential of island-arc volcanic complexes spatially associated with massive sulfide deposits. The systematic study of fluid inclusions in minerals of ores and wall rocks at five massive sulfide deposits of the Verkhneural’sk district furnished evidence that ore-forming fluids had temperature of 375–115°C, pressure up to 1.0–0.5 kbar, chloride composition, and salinity of 0.8–11.2 (occasionally up to 22.8) wt % NaCl equiv. The H and O isotopic compositions of sericite from host metasomatic rocks suggest a substantial contribution of seawater to the composition of mineral-forming fluids. The role of magmatic water increases in the central zones of the feeding conduit and with depth. The dual nature of fluids with the prevalence of their magmatic source is supported by S, C, O, and Sr isotopic compositions. The TC parameters of the formation of massive sulfide deposits are consistent with the data on fluid inclusions from contemporary sulfide mounds on the oceanic bottom.     

The Moreira Gomes deposit of the Cuiú-Cuiú goldfield: Fluid inclusions and stable isotope constraints and implications for the genesis of granite-hosted gold mineralization in the Tapajós Gold Province,Brazil

Moreira Gomes is a recently discovered deposit (21.7 t Au) of the Cuiú-Cuiú goldfield, Tapajós Gold Province, Amazonian Craton. The mineralized zone is about 1200 m long, 30–50 m wide, and at least 400 m in depth. The zone is controlled by a subvertical, east–west-trending structure that is related to a left lateral strike-slip fault system. The host rocks are predominantly tonalites of the Creporizão Intrusive Suite (1997 ± 2 Ma) of uncertain tectonic setting (magmatic arc or post-collision). Hydrothermal alteration and mineralization are predominantly of the fissure-filling type and locally pervasive. Sericitization, chloritization, sulfidation, silicification, carbonatization and epidotization are the observed alteration types. Pyrite is the predominant sulfide mineral and bears inclusions of chalcopyrite, galena, sphalerite and minor hessite and bismuthinite. Gold occurs predominantly as inclusions in pyrite and subordinately in the free-milling state in quartz veins. Ag, Pb and Bi have been detected by semi-quantitative EDS analysis.Three types of fluid inclusions, hosted in quartz veins and veinlets, have been identified. (1) one- and two-phase CO₂ inclusions; (2) two- and three-phase H₂O–CO₂-salt inclusions, and (3) two-phase H₂O-salt inclusions. The CO₂-bearing types are interpreted as the product of phase separation of an immiscible fluid. This fluid presents low to moderate density, low to moderate salinity (1.6–11.8 wt.% NaCl equivalent) and was trapped at 280° to 350 °C. The chemical system of the aqueous inclusions may contain CaCl₂ and/or MgCl₂, salinity varies from zero to 10.1 wt.% NaCl equivalent. Only locally salinities up to 25% have been recorded. This fluid was trapped between 120° and 220 °C and is interpreted as resulting from mixing of a hotter and more saline aqueous fluid (in part derived from phase separation of the H₂O–CO₂ fluid) with a cooler and dilute aqueous fluid.The δ³⁴S values of pyrite (−0.3‰ to 3.9‰) are probably related to magmatic sulfur. The isotopic composition of inclusion fluids and of the fluid in equilibrium with hydrothermal minerals (quartz, chlorite, and calcite) show δ¹⁸O and δD values that range from +0.5 to +9.8‰, and from −49 to −8‰, respectively. Mineral pairs show equilibrium isotopic temperatures that are compatible with the fluid inclusion homogenization temperatures and with textural relationships of the hydrothermal minerals.Isotopic results combined with mineralogical and fluid inclusion data are interpreted to reflect a magmatic-hydrothermal system that evolved in at least three stages. (1) Exsolution of a CO₂-bearing magmatic fluid between 400 °C and 320–350 °C and up to 2.1 kbar (6 km in depth) followed by phase separation and main precipitation of the hydrothermal assemblage composed of chlorite–sericite–pyrite–quartz-gold. (2) Cooling and continuous exsolution of CO₂ produced a CO₂-depleted and slightly more saline aqueous fluid that was trapped mainly at 250°–280 °C. The predominant hydrothermal assemblage of stage 1 continued to form, but epidote is the main phase at this stage. (3) Mixing of the stage 2 aqueous fluid with a cooler and dilute aqueous fluid of meteoric origin, which was responsible for the main carbonatization phase. The mineralizing fluid was neutral to slightly alkaline and relatively reduced. H₂S (and/or HS^-) might have been the main sulfur species in the fluid and Au(HS)^2- was probably the gold transporting complex. Gold deposition occurred as a consequence of a combination of mechanisms, such as phase separation, mixing and fluid-rock interaction.The Moreira Gomes is a granite-hosted gold deposit that is interpreted to be a product of a magmatic-hydrothermal gold system. The age of ore formation (∼1.86 Ga) is consistent with the final stages of evolution of the widespread high-K, calc-alkaline Parauari Intrusive Suite, although the transitional to predominantly alkaline Maloquinha Intrusive Suite cannot be ruled out. Notwithstanding, the deposit does not show the classic features of (oxidized or reduced) intrusion-related gold deposits of Phanerozoic magmatic arcs.     

The mineral–geochemical evidence of contact transformation of ores of the Dzhusinskoe pyrite–polymetallic deposit (Southern Urals)

The Dzhusinskoe pyrite–polymetallic deposit is characterized by an abundant concentration of dykes of basic and intermediate rocks. Thermal metamorphism of ore-host rocks and the recrystallization of ore minerals are associated with the intrusion of post-ore dykes. A regular increase in the homogenization temperature from 156° at a distance from a dyke to 287–305°C in the contact zone was established. Highly saline (6.4–15.7 wt % NaCl eq.) CO₂–H₂O–NaCl fluids under high pressure (up to 1500 bar) can be associated with the processes of contact and regional metamorphism.     

Gold ore-forming fluids of the Tanami region, Northern Australia

Fluid inclusion studies have been carried out on major gold deposits and prospects in the Tanami region to determine the compositions of the associated fluids and the processes responsible for gold mineralization. Pre-ore, milky quartz veins contain only two-phase aqueous inclusions with salinities ≤19 wt% NaCl eq. and homogenization temperatures that range from 110 to 410°C. In contrast, the ore-bearing veins typically contain low to moderate salinity (<14 wt% NaCl eq.), H₂O + CO₂ ± CH₄ ± N₂-bearing fluids. The CO₂-bearing inclusions coexist with two-phase aqueous inclusions that exhibit a wider range of salinities (≤21 wt% NaCl eq.). Post-ore quartz and carbonate veins contain mainly two-phase aqueous inclusions, with a last generation of aqueous inclusions being very CaCl₂-rich. Salinities range from 7 to 33 wt% NaCl eq. and homogenization temperatures vary from 62 to 312°C. Gold deposits in the Tanami region are hosted by carbonaceous or iron-rich sedimentary rocks and/or mafic rocks. They formed over a range of depths at temperatures from 200 to 430°C. The Groundrush deposit formed at the greatest temperatures and depths (260–430°C and ≤11 km), whereas deposits in the Tanami goldfield formed at the lowest temperatures (≥200°C) and at the shallowest depths (1.5–5.6 km). There is also evidence in the Tanami goldfield for late-stage isothermal mixing with higher salinity (≤21 wt% NaCl eq.) fluids at temperatures between 100 and 200°C. Other deposits (e.g., The Granites, Callie, and Coyote) formed at intermediate depths and at temperatures ranging from 240 to 360°C. All ore fluids contained CO₂ ± N₂ ± CH₄, with the more deeply formed deposits being enriched in CH₄ and higher level deposits being enriched in CO₂. Fluids from deposits hosted mainly by sedimentary rocks generally contained appreciable quantities of N₂. The one exception is the Tanami goldfield, where the quartz veins were dominated by aqueous inclusions with rare CO₂-bearing inclusions. Calculated δ ¹⁸O values for the ore fluids range from 3.8 to 8.5‰ and the corresponding δD values range from −89 to −37‰. Measured δ ¹³C values from CO₂ extracted from fluid inclusions ranged from −5.1 to −8.4‰. These data indicate a magmatic or mixed magmatic/metamorphic source for the ore fluids in the Tanami region. Interpretation of the fluid inclusion, alteration, and structural data suggests that mineralization may have occurred via a number of processes. Gold occurs in veins associated with brittle fracturing and other dilational structures, but in the larger deposits, there is also an association with iron-rich rocks or carbonaceous sediments, suggesting that both structural and chemical controls are important. The major mineralization process appears to be boiling/effervescence of a gas-rich fluid, which leads to partitioning of H₂S into the vapor phase resulting in gold precipitation. However, some deposits also show evidence of desulfidation by fluid–rock interaction and/or reduction of the ore-fluid by fluid mixing. These latter processes are generally more prevalent in the higher crustal-level deposits.     

Fluid evolution of the Chalukou giant Mo deposit in the northern Great Xing'an Range,NE China

The Chalukou giant Mo deposit in the Heilongjiang Province, northeastern China, is a porphyry deposit hosted in an intermediate‐felsic complex surrounded by Mesozoic volcano–sedimentary rocks. The mineralization process is composed of four stages, including quartz + K‐feldspar (Stage I), quartz + molybdenite (Stage II), pyrite + chalcopyrite + quartz ± other sulphides (Stage III) and carbonate ± fluorite ± quartz (Stage IV). The mineralization is generally associated with intense K‐feldspar‐, fluorite‐, phyllic‐ and propylitic alteration. Primary fluid inclusions (FIs) in quartz include four compositional types, i.e. pure carbonic (PC‐type), aqueous‐carbonic (C‐type), daughter mineral‐bearing (S‐type) and aqueous (W‐type) inclusions. Halite, sylvite and hematite are recognized as the daughter minerals in Stage I S‐type FIs, whereas molybdenite and chalcopyrite occur as daughter minerals in Stage II S‐type FIs. High‐salinity and high pressure (>220 MPa) FIs exist in Stage I quartz veins, characterized by homogenization through halite dissolution at temperatures of 324 to 517 °C. The paucity of coexisting vapour‐rich FIs with similar homogenization temperatures at this stage indicates that the initial S‐type inclusions have directly exsolved from the magma rather than boiling off of a low‐salinity vapour. Stage I quartz has captured the C‐ and W‐type FIs, which have totally homogenized at 270–530 °C with salinities of 1.6–17.0 wt.% NaCl equiv. At Stage II, the coexistence of all FI types were only observed at pressures of 150–218 MPa and temperatures of 352–375 °C, with two salinity clusters of 0.9–16.6 wt.% NaCl equiv. and 37–56 wt.% NaCl equiv. Stage III quartz contains W‐type FIs with homogenization temperatures of 158–365 °C, salinities of 0.5–9.0 wt.% NaCl equiv., and minimum pressures of 12–116 MPa; whilst Stage IV fluorite or calcite only contains W‐type FIs with homogenization temperatures of 121–287 °C, salinities of 0.5–5.3 wt.% NaCl equiv., and minimum pressures of 10–98 MPa. The estimated trapping pressure from Stages II to III suggests an alternating lithostatic–hydrostatic fluid‐system caused by fluid boiling. Ore fluids at the Chalukou Mo deposit may have been evolved from a CO₂‐rich, high‐salinity, and high‐oxygen fugacity (fO₂) magma system, to a CO₂‐poor, low‐salinity, and low‐fO₂ epithermal system. Two key points may have contributed to the formation of the Chalukou giant Mo deposit: The magmatic origin and fluid boiling that has resulted in decompression and rapid precipitation of metals. Copyright © 2014 John Wiley & Sons, Ltd.     

Multiple origin of the ‘Kniest feeder zone’ of the stratiform Zn–Pb–Cu ore deposit of Rammelsberg, Germany

The Zn–Pb–Cu ore deposit of Rammelsberg is characterized by a complex fluid flow history. The main phase of ore deposition occurred during the Middle Devonian in the Rhenohercynian basin. The Kniest zone underlying the stratiform ore is interpreted as the feeder zone, along which hydrothermal fluids migrated upward and were expelled on the sea floor. Mineralizing brines possibly had a minimum temperature of 130°C, and salinity ranged between 4.9 and 10.3 eq. wt.% NaCl. The ore and its host rock became folded during the Variscan orogeny, and low salinity fluids (1.0 to 2.3 eq. wt.% NaCl) were mobilized during this tectonic period. Remobilization of the ore took place during the Mesozoic by a high salinity (17.3 to 20.2 eq. wt.% NaCl) H₂O–NaCl–CaCl₂ fluid.