U–Pb SHRIMP monazite ages of the giant Morro Velho and Cuiabá gold deposits, Rio das Velhas greenstone belt, Quadrilátero Ferrífero, Minas Gerais, Brazil

U–Pb SHRIMP results of 2672 ± 14 Ma obtained on hydrothermal monazite crystals, from ore samples of the giant Morro Velho and Cuiabá Archean orogenic deposits, represent the first reliable and precise age of gold mineralization associated with the Rio das Velhas greenstone belt evolution, in the Quadrilátero Ferrífero, Brazil. In the basal Nova Lima Group, of the Rio das Velhas greenstone belt, felsic volcanic and volcaniclastic rocks have been dated between 2792 ± 11 and 2751 ± 9 Ma, coeval with the intrusion of syn-tectonic tonalite and granodiorite plutons, and also with the metamorphic overprint of older tonalite–trondhjemite–granodiorite crust. Since cratonization and stable-shelf sedimentation followed intrusion of Neoarchean granites at 2612 + 3/− 2 Ma, it is clear that like other granite–greenstone terranes in the world, gold mineralization is constrained to the latest stages of greenstone evolution.     

The Rio Narcea gold belt intrusions: geology, petrology, geochemistry and timing

This paper discusses the petrographical, mineralogical and geochemical characteristics of the intrusive rocks located along the Rio Narcea Gold Belt, and the timing of formation of the El Valle-Boinás deposit. Rocks in the belt range from quartz-monzodiorites through quartz-monzogranites to monzogranites. The former are made up of pyroxene (clino and ortho), amphibole (magnesiohornblende), biotite, zoned plagioclase (An35-70), and to a lesser degree quartz and K-feldspar. The monzogranites consist of biotite, zoned plagioclase (An30-60), quartz and K-feldspar. All igneous rocks are characterized by the presence of ilmenite and the lack or scarce presence of magnetite indicating their formation under reducing conditions. The granitoids are calc-alkaline I type, potassium-rich and highly reducent with more ferrous than ferric iron. Their characteristics are like the plutons associated with gold and copper (zinc) skarns, but their characteristics reflect more reducent formation conditions, increasing their capacity to form gold skarns.The Boinas granitoid emplacement occurred at about 303±6 Ma and generated calcic and magnesic skarns at the contact with limestone and dolostones of the Láncara Formation. Skarns and granitoids were first altered to amphibole and sericite, respectively, and mineralized at 302±9 Ma. The intrusion of subvolcanic porphyritic dikes produced a second period of alteration at 285±4 Ma, characterized by carbonatization and sericitization of the monzogranites and chloritization and serpentinization of the skarns. The later intrusion of diabasic dikes at 255±6 Ma produced limited carbonatization, silicification and sericitization and hypogene oxidation of the previous stages. Supergene oxidation then occurred at the top of the ore and along fractures and breccias.     

Preliminary mineralogical and petrological study of the Ortosa Au–Bi–Te ore deposit: a reduced gold skarn in the northern part of the Rio Narcea Gold Belt, Asturias, Spain

The Ortosa deposit (NW Spain) in the northern part of the Rio Narcea Gold Belt (RNGB) is located in the Cantabrian Zone of the Iberian Massif. This zone corresponds to the westernmost exposure of the European Hercynides. The deposit is hosted by marine shales, siltstones, calcareous siltstones and interbedded sandy limestones of the upper part of the Silurian Furada Formation. These rocks are intruded by a main stock and numerous sills and dikes consisting of a reduced, ilmenite-bearing quartz-monzodiorite (Ortosa intrusion). Skarn metasomatism and associated gold mineralization overprinted these sedimentary and igneous rocks, forming endo- and exoskarns.The earliest stage of alteration involved potassium metasomatism from which metasomatic biotite developed in the hornfels around the intrusion. In the endoskarn, the first metasomatic mineral to form is actinolite. Subsequently, quartz, pyroxene (Hd_30–45), and sulfides (mainly arsenopyrite and pyrrhotite) formed, followed by a second generation of amphibole (ferroactinolite and ferrohornblende). The exoskarn is a pyroxene-garnet skarn, which is often banded. The prograde minerals are pyroxene (Hd_10–30) and grossular garnet. The retrograde mineralogy consists of hedenbergite-rich pyroxene (Hd_50–87), amphibole (ferroactinolite–ferrohornblende), and the metallic minerals with minor fluorapatite, K-feldspar, albite, epidote–clinozoisite, vesuvianite and calcite. A final stage of retrograde alteration is characterized by calcite, quartz, and chlorite.Pyrrhotite and arsenopyrite are the more abundant metallic minerals, and löllingite, chalcopyrite, pyrite and sphalerite are present in smaller amounts. The gold occurs as native gold and maldonite, and is accompanied by hedleyite, native bismuth, and bismuthinite. These Au–Bi–Te mineral assemblages occupy cavities and fractures in the arsenopyrite or in the pyrrhotite.Estimated physiochemical conditions of formation based on the composition and stability fields of major calc-silicate and sulfide minerals indicate that the hedenbergite-rich pyroxene and the earliest sulfides (löllingite–pyrrhotite–arsenopyrite) crystallized at temperatures between 470 and 535°C at low log fS₂ between −10 and −6.5 and low log fO₂ of −22. The Ortosa skarns can be included in the reduced gold skarn subtype defined by Meinert (Mineralogical Association of Canada, Quebec city, Que., Canada, 1998, 26,359–414 ).     

Molybdenite Re–Os and albite Ar/Ar dating of Cu–Au–Mo and magnetite porphyry systems in the Yangtze River valley and metallogenic implications

The area of the Middle–Lower Yangtze River valley, Eastern China, extending from Wuhan (Hubei province) to western Zhenjiang (Jiangsu province), hosts an important belt of Cu–Au–Mo and Fe deposits. There are two styles of mineralization, i.e., skarn/porphyry/stratabound Cu–Au–Mo–(Fe) deposits and magnetite porphyry deposits in several NNE-trending Cretaceous fault-bound volcanic basins. The origin of both deposit systems is much debated. We dated 11 molybdenite samples from five skarn/porphyry Cu–Au–Mo deposits and 5 molybdenite samples from the Datuanshan stratabound Cu–Au–Mo deposit by ICP-MS Re–Os isotope analysis. Nine samples from the same set were additionally analyzed by NTIMS on Re–Os. Results from the two methods are almost identical. The Re–Os model ages of 16 molybdenite samples range from 134.7 ± 2.3 to 143.7 ± 1.6 Ma (2σ). The model ages of the five samples from the Datuanshan stratabound deposit vary from 138.0 ± 3.2 to 140.8 ± 2.0 Ma, with a mean of 139.3 ± 2.6 Ma; their isochron age is 139.1 ± 2.7 Ma with an initial Os ratio of 0.7 ± 8.1 (MSWD = 0.29). These data indicate that the porphyry/skarn systems and the stratabound deposits have the same age and suggest an origin within the same metallogenic system. Albite ⁴⁰Ar/³⁹Ar dating of the magnetite porphyry deposits indicates that they formed at 123 to 125 Ma, i.e., 10–20 Ma later. Both mineralization styles characterize transitional geodynamic regimes, i.e., the period around 140 Ma when the main NS-trending compressional regime changed to an EW-trending lithospheric extensional regime, and the period of 125–115 Ma of dramatic EW-trending lithospheric extension.     

The Carlés copper–gold–molybdenum skarn (Asturias, Spain): geometry, mineral associations and metasomatic evolution

This paper presents the petrographical, mineralogical and geochemical characteristics of the Carlés Cu–Mo–Au ore deposit, located in the Rio Narcea Gold Belt (Cantabrian zone of the Iberian Massif). It is related to a small postkinematic calc-alkaline monzogranite, which intrudes as a cedar-tree laccolith into the upper siliciclastic Furada Formation (late Silurian age) and the Nieva carbonates (early Devonian age). The Carlés deposit consists mainly of a well-developed exoskarn. The exoskarn is mostly calcic skarn made up of early garnet and pyroxene, and later amphibole, magnetite and sulfides. The presence of magnesian skarn has been recorded on the north side of the intrusion (roof of granitoid). Magnesian skarn consists of olivine, which is partially replaced by diopside and phlogopite and spinel. Close to the igneous rock, skarns are overprinted by strong potassic alteration. The ore is related to the skarn retrogradation and post-skarn veining and faulting. The skarn-related ore consists of earlier, uneconomic magnetite and Fe–As sulfide assemblages and economic Cu–Au–Ag (Bi–Te) assemblages on the eastern and western sides of the contact aureole, and uneconomic Mo and subeconomic Fe–As–Cu–Au–Ag on the northern side of the contact. Later subeconomic Fe–As–Sb–(Zn–Sn–Cu–Au–Ag) assemblages crosscut the granitoid, skarn, marbles and mineral associations developed previously, and are related to younger episodes of fracturing and faulting. Fluid inclusions in the first hydrothermal stage consist of an aqueous solution with significant contents of CO₂, which reach unmixing conditions as a result of a decrease in P–T conditions. This led to two types of solutions, aqueous solutions of moderate to high salinity and hydrocarbon solutions of low salinity. This unmixing phenomenon controlled the first stage of gold precipitation. During the late hydrothermal activity, primary low-salinity-aqueous-carbonic inclusions with contrasting densities are found. They homogenize into vapor, critical or liquid phase. Homogenization temperatures are practically the same in all inclusions, indicating a boiling phenomenon that could control a new precipitation of gold.     

P–T conditions of mineralization in the Jonnagiri granitoid-hosted gold deposit, eastern Dharwar Craton, southern India: Constraints from fluid inclusions and chlorite thermometry

Gold mineralization at Jonnagiri, Dharwar Craton, southern India, is hosted in laminated quartz veins within sheared granodiorite that occur with other rock units, typical of Archean greenstone–granite ensembles. The proximal alteration assemblage comprises of muscovite, plagioclase, and chlorite with minor biotite (and carbonate), which is distinctive of low- to mid-greenschist facies. The laminated quartz veins that constitute the inner alteration zone, contain muscovite, chlorite, albite and calcite. Using various calibrations, chlorite compositions in the inner and proximal zones yielded comparable temperature ranges of 263 to 323 °C and 268 to 324 °C, respectively. Gold occurs in the laminated quartz veins both as free-milling native metal and enclosed within sulfides. Fluid inclusion microthermometry and Raman spectroscopy in quartz veins within the sheared granodiorite in the proximal zone and laminated auriferous quartz veins in inner zone reveal the existence of a metamorphogenic aqueous–gaseous (H₂O–CO₂–CH₄ + salt) fluid that underwent phase separation and gave rise to gaseous (CO₂–CH₄), low saline (~ 5 wt.% NaCl equiv.) aqueous fluids. Quartz veins within the mylonitized granodiorites and the laminated veins show broad similarity in fluid compositions and P–T regime. Although the estimated P–T range (1.39 to 2.57 kbar at 263 to 323 °C) compare well with the published P–T values of other orogenic gold deposits in general, considerable pressure fluctuation characterize gold mineralization at Jonnagiri. Factors such as fluid phase separation and fluid–rock interaction, along with a decrease in f(O₂), were collectively responsible for gold precipitation, from an initial low-saline metamorphogenic fluid. Comparison of the Jonnagiri ore fluid with other lode gold deposits in the Dharwar Craton and major granitoid-hosted gold deposits in Australia and Canada confirms that fluids of low saline aqueous–carbonic composition with metamorphic parentage played the most dominant role in the formation of the Archean lode gold systems.     

Sn-polymetallic greisen-type deposits associated with late-stage rapakivi granites, Brazil: fluid inclusion and stable isotope characteristics

Tin-polymetallic greisen-type deposits in the Itu Rapakivi Province and Rondônia Tin Province, Brazil are associated with late-stage rapakivi fluorine-rich peraluminous alkali-feldspar granites. These granites contain topaz and/or muscovite or zinnwaldite and have geochemical characteristics comparable to the low-P sub-type topaz-bearing granites. Stockworks and veins are common in Oriente Novo (Rondônia Tin Province) and Correas (Itu Rapakivi Province) deposits, but in the Santa Bárbara deposit (Rondônia Tin Province) a preserved cupola with associated bed-like greisen is predominant. The contrasting mineralization styles reflect different depths of formation, spatial relationship to tin granites, and different wall rock/fluid proportions. The deposits contain a similar rare-metal suite that includes Sn (±W, ±Ta, ±Nb), and base-metal suite (Zn–Cu–Pb) is present only in Correas deposit. The early fluid inclusions of the Correas and Oriente Novo deposits are (1) low to moderate-salinity (0–19 wt.% NaCl eq.) CO₂-bearing aqueous fluids homogenizing at 245–450 °C, and (2) aqueous solutions with low CO₂, low to moderate salinity (0–14 wt.% NaCl eq.), which homogenize between 100 and 340 °C. In the Santa Bárbara deposit, the early inclusions are represented by (1) low-salinity (5–12 wt.% NaCl eq.) aqueous fluids with variable CO₂ contents, homogenizing at 340 to 390 °C, and (2) low-salinity (0–3 wt.% NaCl eq.) aqueous fluid inclusions, which homogenize at 320–380 °C. Cassiterite, wolframite, columbite–tantalite, scheelite, and sulfide assemblages accompany these fluids. The late fluid in the Oriente Novo and Correas deposit was a low-salinity (0–6 wt.% NaCl eq.) CO₂-free aqueous solution, which homogenizes at (100–260 °C) and characterizes the sulfide–fluorite–sericite association in the Correas deposit. The late fluid in the Santa Bárbara deposit has lower salinity (0–3 wt.% NaCl eq.) and characterizes the late-barren-quartz, muscovite and kaolinite veins. Oxygen isotope thermometry coupled with fluid inclusion data suggest hydrothermal activity at 240–450 °C, and 1.0–2.6 kbar fluid pressure at Correas and Oriente Novo. The hydrogen isotope composition of breccia-greisen, stockwork, and vein fluids (δ¹⁸O_quartz from 9.9‰ to 10.9‰, δD_H2O from 4.13‰ to 6.95‰) is consistent with a fluid that was in equilibrium with granite at temperatures from 450 to 240 °C. In the Santa Bárbara deposit, the inferred temperatures for quartz-pods and bed-like greisens are much higher (570 and 500 °C, respectively), and that for the cassiterite-quartz-veins is 415 °C. The oxygen and hydrogen isotope composition of greisen and quartz-pods fluids (δ¹⁸O_qtz-H2O=5.5–6.1‰) indicate that the fluid equilibrated with the albite granite, consistent with a magmatic origin. The values for mica (δ¹⁸O_mica-H2O=3.3–9.8‰) suggest mixing with meteoric water. Late muscovite veins (δ¹⁸O_qtz-H2O=−6.4‰) and late quartz (δ¹⁸O_mica-H2O=−3.8‰) indicate involvement of a meteoric fluid. Overall, the stable isotope and fluid inclusion data imply three fluid types: (1) an early orthomagmatic fluid, which equilibrated with granite; (2) a mixed orthomagmatic-meteoric fluid; and (3) a late hydrothermal meteoric fluid. The first two were responsible for cassiterite, wolframite, and minor columbite–tantalite precipitation. Change in the redox conditions related to mixing of magmatic and meteoric fluids favored important sulfide mineralization in the Correas deposit.     

马坑铁钼铅锌多金属矿成矿流体演化及矿床成因类型

马坑铁矿是福建省一个大型铁钼铅锌多金属矿床,赋存于莒舟-大洋花岗岩外接触带上石炭统经畲组-下二叠统栖霞 组大理岩与下石炭统林地组石英砂岩之间,矿化阶段经历了从无水矽卡岩阶段（钙铁榴石-透辉石） →含水矽卡岩-磁铁矿 阶段（绿帘石-阳起石-绿泥石-钙铁辉石） →硫化物阶段（石英-方解石-萤石-黄铁矿-闪锌矿） →碳酸盐岩阶段（石英-方 解石） 演变,而本文对含水矽卡岩-磁铁矿阶段和硫化物阶段中的钙铁辉石、萤石、石英及方解石中流体包裹体所进行岩 相学观察和显微测温研究表明,早期含水矽卡岩-磁铁矿阶段包裹体类型主要有含NaCl子晶三相包裹体和富液相两相包裹 体,少量富气相两相包裹体;而晚期硫化物阶段包裹体类型主要为富液相两相包裹体。含水矽卡岩-磁铁矿阶段流体出现 流体沸腾作用,流体温度范围为448~596℃,两端员组分流体盐度分别为26.5~48.4 wt % NaCl equiv.和2.4~6.9 wt % NaCl equiv.;硫化物阶段流体呈现出混合趋势,流体温度和盐度分别为182~343℃和1.9~20.1 wt % NaCl equiv.。流体包裹体的均 一温度和盐度的研究结果表明含水矽卡岩-磁铁矿阶段流体主要来自岩浆水,而硫化物阶段流体以岩浆水为主,并有大气 降水加入。由于马坑铁矿化形成于含水矽卡岩阶段,铅锌矿化则形成于硫化物阶段,流体沸腾是导致马坑铁矿床形成的主 要因素,而流体混合则是引起马坑铁矿床铅锌矿化的主要因素。综合地质与地球化学研究,马坑铁矿床应属于与莒舟-大 洋花岗岩有关的矽卡岩型铁矿床。     

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 Nucleus Deposit: Superposed Au–Ag–Bi–Cu Mineralization Systems at Freegold Mountain,Yukon, Canada

In this paper we present titanite U–Pb (both single crystal CA ID‐TIMS and in situ LA ICP‐MS) data, coupled with ore and gangue mineralogy and geochemical (both lithogeochemistry and microanalysis) data from the Nucleus Au–Ag–Bi–Cu deposit, in the Yukon (Canada) portion of the Tintina Au province. Arsenic‐bearing Au–Ag–Bi–Cu mineralization at Nucleus consists of two distinct styles of mineralization including: (i) reduced Au skarn and sulfide replacement; and (ii) a relatively shallow‐emplaced (as supported by textures and temperature of formation), vein‐controlled mineralization occurring mainly as veins and veinlets of various shapes (sheeted, single, stockworks, and crustiform), breccias, and disseminations. Whereas Au, Bi, and Cu mineralization from skarn is associated with hydrous retrograde alteration phases (actinolite, ferro‐actinolite, hastingsite, cannilloite, and hornblende), numerous alteration types are associated with the vein‐controlled style of mineralization and these include: biotite, phyllic, argillic, propylitic, carbonate, and quartz (silicification) alterations. The mineralization–alteration processes took place over a wide temperature range that is bracketed between 340 and 568°C, as indicated by chlorite and arsenopyrite geothermometers. The Au‐rich Nucleus deposit is characterized by anomalously high content of As and Bi (as much as 1 %), and whereas Au moderately correlates with Bi (r = 0.40) in the skarn mineralization style (where native Au is spatially associated with native Bi and Bi‐bearing sulfides), the two elements correlate poorly (r = 0.14) in the vein‐controlled type, in which native Bi‐ and Bi‐sulfide‐bearing veins are locally observed. Sphalerite from the vein‐controlled mineralized type is Fe‐rich (9.92–10.54 mol % FeS) indicative of low sulfidation conditions, as well as high temperature, with the latter further supported by arsenopyrite geothermometry (up to 491°C), low Ag content (3–7 wt.%) in Au, and the high gold fineness (926–964). Whereas molybdenite Re–Os ages from quartz‐molybdenite veins range from 75.8 to 76.2 ± 0.3 Ma, titanite from the skarn type mineralization recorded CA ID‐TIMS and LA ICP‐MS U–Pb ages of 182.6 ± 2.4 Ma and 191.0 ± 1.5 Ma, respectively, thus precluding any genetic link between the two spatially associated styles of mineralization from the Nucleus deposit area. The Au–Ag–Bi–Cu Nucleus deposit is therefore regarded as a superposed system in which two mineralization types, without any petrogenetic relationship, overlapped, possibly with remobilization of early‐formed mineralization.     

Mineral assemblages of the Francisco I. Madero Zn–Cu–Pb–(Ag) deposit, Zacatecas, Mexico: Implications for ore deposit genesis

The Francisco I. Madero deposit, central Mexico, occurs in the Mesozoic Guerrero Terrane, which hosts many ore deposits, both Cretaceous (volcanogenic massive sulfides) and Tertiary (epithermal and skarn deposits). It is hosted by a 600 m-thick calcareous-pelitic unit, of Lower Cretaceous age, crosscut by porphyritic dikes that strike NW–SE. A thick felsic volcanic Tertiary sequence, consisting of andesites and rhyolitic ignimbrites, unconformably overlies the Cretaceous series. At the base, the mineralization consists of several mantos developed within calcareous beds. They are dominantly composed of sphalerite, pyrrhotite and pyrite with minor chalcopyrite, arsenopyrite and galena. At the top of the orebody, there are calcic skarns formed through prograde and retrograde stages. The resulting mineral assemblages are rich in manganoan hedenbergite (Hd_75–28Di_40–4Jh_40–20), andraditic garnets (Adr_100–62Grs_38–0), epidote (Ep_95–36Czo_60–5Pie_8–0), chamosite, calcite and quartz. The temperature of ore deposition, estimated by chlorite and arsenopyrite geothermometry, ranges from 243° to 277 °C and from 300° to 340 °C, respectively. The pressure estimated from sphalerite geobarometry averages 2.1 kbar. This value corresponds to a moderately deep skarn and agrees with the high Cu content of the deposit. Paragenesis, P–T conditions and geological characteristics are compatible with a distal, dike-related, Zn skarn deposit. Its style of mineralization is similar to that of many high-temperature carbonate replacement skarn deposits in the Southern Cordillera.     

Copper mineralization around the Ahar batholith, north of Ahar (NW Iran): Evidence for fluid evolution and the origin of the skarn ore deposit

This investigation presents and interprets fluid inclusion data from different lithological units of the Cu skarn deposits at Mazraeh, north of Ahar, Azarbaijan, NW Iran. The results provide an assessment of the P–T conditions and mineral–fluid evolution and suggest new exploration parameters. Five types of inclusions are recognized from quartz and garnet. The temperature of homogenization of Type I inclusions with daughter minerals halite and sylvite ranges from 312° to 470 °C with total salinity of 52 to 63 wt.% NaCl equiv.; Type II and III inclusions with halite have homogenization temperatures of 230° to 520 °C and salinity of 31 to 50 wt.% NaCl equiv. The salinity of Types IV and V biphase (liquid + vapor) inclusions, based on their final ice melting temperature, varies between 10.2 to 20.8 wt.% NaCl equiv. T_h vs. salinity plots of inclusions show that the salinity of the fluids correlates positively with temperature. The inclusions formed at low pressure. Changes in the temperature and salinity of the fluids can be reconstructed from the inclusions. Highly saline, high-temperature fluids were most abundant during the main chalcopyrite ore-forming phase in the skarn and mineralized quartz veins. Low-salinity aqueous fluids were abundant in barren veins, in which there is no evidence for early hot high-salinity brine, and might have resulted from late-stage dilution and mixing of hydrothermal fluids with meteoric water. Based on petrographic features and fluid-inclusion data, early-stage magnetite deposition is related to boiling of fluid at temperatures of about 500 °C. At a later stage, boiling at temperatures of around 320° to 400 °C favored the deposition of sulfides and Fe mobility was decreased at these lower temperatures. The following inclusion characteristics may be used as exploration parameters in the Mazraeh area. (i) Presence of high-temperature, salt-bearing inclusions, with T_h between 300 and 500 °C; (ii) High-salinity fluid inclusions; and (iii) Inclusions showing evidence of boiling of the fluid. In addition, the presence of magnetite is an important exploration parameter.     

The sandstone-hosted stratiform copper mineralization at Mwitapile and its relation to the mineralization at Lufukwe, Lufilian foreland, Democratic Republic of Congo

The Lufilian foreland is a triangular-shaped area located in the SE of the Democratic Republic of Congo and to the NE of the Lufilian arc, which hosts the well-known Central African Copperbelt. The Lufilian foreland recently became an interesting area with several vein-type (e.g., Dikulushi) and stratiform (e.g., Lufukwe and Mwitapile) copper occurrences. The Lufilian foreland stratiform Cu mineralization is, to date, observed in sandstone rock units belonging to the Nguba and Kundelungu Groups (Katanga Supergroup).The Mwitapile sandstone-hosted stratiform Cu prospect is located in the north eastern part of the Lufilian foreland. The host rock for the Cu mineralization is the Sonta Sandstone of the Ngule Subgroup (Kundelungu Group). A combined remote sensing, petrographic and fluid inclusion microthermometric analysis was performed at Mwitapile and compared with similar analysis previously carried out at Lufukwe to present a metallogenic model for the Mwitapile- and Lufukwe-type stratiform copper deposits. Interpretation of ETM+ satellite images for the Mwitapile prospect and the surrounding areas indicate the absence of NE–SW or ENE–WSW faults, similar to those observed controlling the mineralization at Lufukwe. Faults with these orientations are, however, present to the NW, W, SW and E of the Mwitapile prospect. At Mwitapile, the Sonta Sandstone host rock is intensely compacted, arkosic to calcareous with high silica cementation (first generation of authigenic quartz overgrowths). In the Sonta Sandstone, feldspar and calcite are present in disseminated, banded and nodular forms. Intense dissolution of these minerals caused the presence of disseminated rectangular, pipe-like and nodular dissolution cavities. Sulfide mineralization is mainly concentrated in these cavities. The hypogene sulfide minerals consist of two generations of pyrite, chalcopyrite, bornite and chalcocite, separated by a second generation of authigenic quartz overgrowth. The hypogene sulfide minerals are replaced by supergene digenite and covellite. Fluid inclusion microthermometry on the first authigenic quartz phase indicates silica precipitation from an H₂O–NaCl–CaCl₂ fluid with a minimum temperature between 111 and 182 °C and a salinity between 22.0 and 25.5 wt.% CaCl₂ equiv. Microthermometry on the second authigenic quartz overgrowths and in secondary trails related to the mineralization indicate that the mineralizing fluid is characterized by variable temperatures (Th = 120 to 280 °C) and salinities (2.4 to 19.8 wt.% NaCl equiv.) and by a general trend of increasing temperatures with increasing salinities.Comparison between Mwitapile and Lufukwe indicates that the stratiform Cu mineralization in the two deposits is controlled by similar sedimentary, diagenetic and structural factors and likely formed from a similar mineralizing fluid. A post-orogenic timing is proposed for the mineralization in both deposits. The main mineralization controlling factors are grain size, clay and pyrobitumen content, the amount and degree of feldspar and/or calcite dissolution and the presence of NE–SW to ENE–WSW faults. The data support a post-orogenic fluid-mixing model for the Mwitapile- and Lufukwe-type sandstone-hosted stratiform Cu deposits, in which the mineralization is related to the mixing between a Cu-rich hydrothermal fluid, with a temperature up to 280 °C and a maximum salinity of 19.8 wt.% NaCl equiv., with a colder low salinity reducing fluid present in the sandstone host rock. The mineralizing fluid likely migrated upwards to the sandstone source rocks along NE–SW to ENE–WSW orientated faults. At Lufukwe, the highest copper grades at surface outcrops and boreholes were found along and near to these faults. At Mwitapile, where such faults are 2 to 3 km away, the Cu grades are much lower than at Lufukwe. Copper precipitation was possibly promoted by reduction from pre-existing hydrocarbons and non-copper sulfides and by the decrease in fluid salinity and temperature during mixing. Based on this research, new Cu prospects were proposed at Lufukwe and Mwitapile and a set of recommendations for further Cu exploration in the Lufilian foreland is presented.     

Neoproterozoic to Early Cambrian history of an active plate margin in the Teplá–Barrandian unit—a correlation of U–Pb isotopic-dilution-TIMS ages (Bohemia, Czech Republic)

The Teplá–Barrandian unit (TBU) of the Bohemian Massif shared a common geological history throughout the Neoproterozoic and Cambrian with the Avalonian–Cadomian terranes. The Neoproterozoic evolution of an active plate margin in the Teplá–Barrandian is similar to Avalonian rocks in Newfoundland, whereas the Cambrian transtension and related calc-alkaline plutons are reminiscent of the Cadomian Ossa–Morena Zone and the Armorican Massif in western Europe. The Neoproterozoic evolution of the Teplá–Barrandian unit fits well with that of the Lausitz area (Saxothuringian unit), but is significantly distinct from the history of the Moravo–Silesian unit.The oldest volcanic activity in the Bohemian Massif is dated at 609+17/−19 Ma (U–Pb upper intercept). Subduction-related volcanic rocks have been dated from 585±7 to 568±3 Ma (lower intercept, rhyolite boulders), which pre-dates the age of sedimentation of the Cadomian flysch ( t chovice Group). Accretion, uplift and erosion of the volcanic arc is documented by the Neoproterozoic Dob í conglomerate of the upper part of the flysch. The intrusion age of 541+7/−8 Ma from the Zgorzelec granodiorite is interpreted as a minimum age of the Neoproterozoic sequence. The Neoproterozoic crust was tilted and subsequently early Cambrian intrusions dated at 522±2 Ma (T ovice granite), 524±3 Ma (V epadly granodiorite), 523±3 Ma (Smr ovice tonalite), 523±1 Ma (Smr ovice gabbro) and 524±0.8 Ma (Orlovice gabbro) were emplaced into transtensive shear zones.     

内蒙古克什克腾旗长岭子铅锌矿床流体包裹体及矿床成因类型研究

内蒙古克什克腾旗长岭子铅锌矿床是大兴安岭南段新发现的一个矿床,矿体赋存于下二叠统大石寨组海相火山岩建造中,矿体受夕卡岩控制。根据手标本中脉体穿插关系和岩石薄片中观察的矿物共生组合特征,文中将长岭子铅锌矿的成矿过程划分为4个阶段：干夕卡岩阶段、湿夕卡岩磁铁矿阶段、石英硫化物阶段和石英碳酸盐阶段,分别以石榴子石±透辉石±硅灰石、石英+绿帘石+电气石+磁铁矿、石英+黄铁矿±磁黄铁矿±黄铜矿±方铅矿±闪锌矿和石英±方解石的矿物组合为标志。长岭子矿床主要发育水溶液包裹体(W型)和含子矿物多相包裹体(S型),前者可进一步划分为富液相(WL型)和富气相(WV型)两个亚类。干夕卡岩阶段辉石中主要发育S型和WL型包裹体,湿夕卡岩磁铁矿阶段绿帘石和石英中主要发育WL型、WV型和S型包裹体,石英硫化物阶段石英中可见所有类型的包裹体,石英碳酸盐阶段的石英±方解石脉中仅见WL型包裹体。干夕卡岩阶段辉石中流体包裹体的均一温度和盐度分别为387~524 ℃和10.7%~52%(NaCleqv.);湿夕卡岩磁铁矿阶段包裹体均一温度为312~533 ℃,盐度为11.3%~60%(NaCleqv.);石英硫化物阶段包裹体均一温度介于182~329 ℃,盐度介于4.7%~38%(NaCleqv.);石英碳酸盐阶段包裹体均一温度为124~199 ℃,盐度介于3.1%~22.4%(NaCleqv.)。上述矿床地质和成矿流体特征表明长岭子铅锌矿为夕卡岩型矿床。成矿流体经历了自夕卡岩阶段高温、高盐度岩浆热液向石英碳酸盐阶段低温、低盐度大气降水热液的转变。石英硫化物阶段发育沸腾包裹体组合,表明成矿流体发生了沸腾作用,这可能是成矿物质沉淀的主要机制。     

Siderite mineralization of the Gemericum superunit (Western Carpathians, Slovakia): review and a revised genetic model

The Gemericum is a segment of the Variscan orogen subsequently deformed by the Alpine–Carpathian orogeny. The unit contains abundant siderite–sulphide and quartz–antimony veins together with stratabound siderite replacement deposits in limestones and stratiform sulphide mineralization in volcano-sedimentary sequences. The siderite–sulphide veins and siderite replacement deposits of the Gemericum represent one of the largest accumulations of siderite in the world, with about 160 million tonnes of mineable FeCO₃. More than 1200 steeply dipping hydrothermal veins are arranged in a regional tectonic and compositional pattern, reflecting the distribution of regional metamorphic zones. Siderite–sulphide veins are typically contained in low-grade (chlorite zone) sedimentary, volcano-sedimentary or volcanic Lower and Upper Paleozoic rocks. Quartz–antimony veins are hosted by higher-grade units (biotite zone). Siderite–sulphide veins are dominated by early siderite followed by a complex set of stages, including quartz–sulphide (chalcopyrite, tetrahedrite), barite, tourmaline–quartz, and sulphide-remobilization stages. The temporal evolution of these stages is difficult to study because of the widespread and repeated tectonic processes, within-vein replacement and recrystallization. Siderite–sulphide veins show considerable vertical (up to 1200 m) and lateral (up to 15 km) extent, and a thickness typically reaching several metres. Carbonate-replacement siderite deposits of the Gemericum are hosted by a Silurian limestone belt and are similar to stratabound siderite deposits of the Eastern Alps (e.g., Erzberg, Austria).Based on a review of geological, petrological and geochronological data for the Gemericum, and extensive stable and radiogenic isotope data and fluid inclusion data on hydrothermal minerals, the siderite–sulphide veins and siderite replacement deposits are classified as metamorphogenic in a broad sense. The deposits were formed during several stages of regional crustal-scale fluid flow. Isotope (S, C, Sr, Pb) fingerprinting identifies the metamorphosed rock complexes of the Gemericum as a source of most components of hydrothermal fluids. Fluid inclusion and stable isotope data evidence the participation of several contrasting fluid types, and the existence of contrasting P–T conditions during vein evolution. A high-δ¹⁸O, medium- to high-salinity, H₂O-type fluid is the most important component during siderite deposition, whereas H₂O–CO₂-type fluid inclusion containing dense liquid CO₂ and corresponding to minimal pressures between 1 and 3 kbar were found in a younger tourmaline–quartz stage. Younger quartz–ankerite(±siderite)–sulphide stages are characterized by high-salinity (17 to 35 wt.% NaCl equivalent) and low-temperature (T_h=90 to 180 °C) H₂O-type fluids.The vein deposits are interpreted as a result of multistage hydrothermal circulation, with Variscan and Alpine mineralization phases. Based on available indirect data, the most important mineralization phase was related to regional fluid flow during the uplift of a Variscan metamorphic core complex, producing siderite–sulphide (±barite) mineralization, while tourmaline–quartz stage and sulphide remobilization stages are related to Alpine processes. Two phases of vein evolution are evident from two groups of ⁸⁷Sr/⁸⁶Sr isotope ratios of Sr-rich, Rb-poor hydrothermal minerals: 0.71042–0.71541 in older barite and 0.7190–0.7220 in late-stage celestine and strontianite.     

Temporal relationship between granite cooling and hydrothermal uranium mineralization at Dalongshan in China: a combined radiometric and oxygen isotopic study

A combined study using multi-radiometric dating and oxygen isotopic geothermometry was carried out for Mesozoic quartz syenite, alkali-feldspar granite and associated hydrothermal uranium mineralization at Dalongshan in the Middle-Lower Yangtze valley of east-central China. Radiometric dating of the quartz syenite yields a whole-rock Rb–Sr isochron age of 135.6±4.3 Ma, a zircon U–Pb isochron age of 132.9±2.2 Ma, and K–Ar ages of 126±2, 118±3 and 94±4 Ma for hornblende, biotite and orthoclase, respectively. The alkali-feldspar granite yields a whole-rock Rb–Sr isochron age of 117.3±3.3 Ma, a zircon U–Pb isochron age of 114.7±2.1 Ma, and K–Ar ages of 112±2, 109±3 and 88±4 Ma for hornblende, biotite and orthoclase, respectively. Oxygen isotope thermometry for both granites gives temperatures of 685 to 720, 555 to 580, 435 to 460 and 320 to 330 °C, for hornblende, magnetite, biotite and orthoclase respectively, when paired with quartz. The systematic differences among the ages by the different techniques on the different minerals are used to reconstruct the cooling history of the granite. The results yield rapid cooling rates of 27.4 to 58.6 °C/Ma from 800 to 300 °C in the early stage, but slow cooling rates of 6.3 to 7.2 °C/Ma from 300 to 150 °C in the late stage. The regular sequence of oxygen isotope temperatures for the different quartz–mineral pairs demonstrates that diffusion is a dominant factor controlling the closure of both radiometric and O isotopic systems during granite cooling. Pitchblende U–Pb isochron dating yields an uranium mineralization age of 106.4±2.9 Ma, which is younger than the age of the granite emplacement and thus considerably postdates the time of magma crystallization, but is close to the closure time of the K–Ar system in the biotite. This points to a close relationship between granite cooling and ore-forming process. It appears that hydrothermal mineralization took place in the stage of slow cooling of the granite, whereas the rapid cooling of the granite was concurrent with the migration of hydrothermal fluids along fault structures. Therefore, the activity of the ore-forming hydrothermal system is temporally dictated by the cooling rates of the granite and may lag about 25 to 30 Ma behind the crystallization timing of associated granite.     

Two Cu–Co sulfide phases and contrasting fluid systems in the Katanga Copperbelt, Democratic Republic of Congo

The Katanga Copperbelt is the Congolese part of the well-known Central African Copperbelt, the largest sediment-hosted stratiform Cu–Co province on Earth. Petrographic examination of borehole samples from the Kamoto and Luiswishi mines in the Katanga Copperbelt recognized two generations of hypogene Cu–Co sulfides and associated gangue minerals (dolomite and quartz). The first generation is characterized by fine-grained Cu–Co sulfides and quartz replacing dolomite. The second generation is paragenetically later and characterized by coarse-grained Cu–Co sulfides and quartz overgrown and partly replaced by dolomite. Fluid inclusion microthermometric data were collected from two different types of fluid inclusions: type-I fluid inclusions (liquid + vapor) in the quartz of the first generation and type-II fluid inclusions (liquid + vapor + halite) in the quartz of the second generation. The microthermometric analyses indicate that the fluids represented by type-I and type-II fluid inclusions had very different temperatures and salinities and were not in thermal equilibrium with the host rock.Petrographic and microthermometric data indicate the presence of at least two main hypogene Cu–Co sulfide phases in the Katanga Copperbelt. The first is an early diagenetic typical stratiform phase, which produced fine-grained sulfides that are disseminated in the host rock and frequently concentrated in nodules and lenticular layers. This phase is related to a hydrothermal fluid with a moderate temperature (115 to 220 °C, or less if reequilibration of inclusions has occurred) and salinity (11.3 to 20.9 wt.% NaCl equiv.). The second hypogene Cu–Co phase produced syn-orogenic coarse-grained sulfides, which also occur disseminated in the host rock but mainly concentrated in a distinct type of stratiform nodules and layers and in stratabound veins and tectonic breccia cement. This second phase is related to a hydrothermal fluid with high temperature (270 to 385 °C) and salinity (35 to 45.5 wt.% NaCl equiv.).A review of available microthermometric and ore geochronological data of the Copperbelt in both the Democratic Republic of Congo and Zambia supports the regional presence of the two Cu–Co phases proposed in our study. Future geochemical analyses in the Copperbelt should take into account the presence of, at least, these two Cu–Co phases, their contrasting fluid systems and the possible overprint of the first phase by the second one.     

Geochronological framework of the Quadrilátero Ferrífero, with emphasis on the age of gold mineralization hosted in Archean greenstone belts

Archean terrains of the Quadrilátero Ferrífero comprise a greenstone belt association surrounded by granitoid–gneiss complexes, mainly composed of banded TTG gneisses whose igneous protoliths are older than 2900 Ma. This early continental crust was affected by three granitic magmatic episodes during the Neoarchean: ca. 2780 to 2760 Ma; 2720 to 2700 Ma; and 2600 Ma. Dating of felsic volcanic and volcaniclastic rocks defines a felsic magmatic event within the greenstone belt association around 2772 Ma, contemporaneous with emplacement of several of the granitic plutons and constrains a major magmatic and tectonic event in the Quadrilátero Ferrífero. Lead isotopic studies of lode–gold deposits indicate that the main mineralization episode occurred at about 2800 to 2700 Ma.Proterozoic evolution of the Quadrilátero Ferrífero comprises deposition of a continental-margin succession hosting thick, Lake Superior-type banded iron formations, at ca. 2500 to 2400 Ma, followed by deposition of syn-orogenic successions after 2120 Ma. The latter is related to the Transamazonian Orogeny. The western part of the Quadrilátero Ferrífero was also affected by the Brasiliano Orogeny (600 to 560 Ma).     

Overheated, Cu-bearing magmas in the Zaldívar porphyry-Cu deposit, Northern Chile. Geodynamic consequences

The Zaldívar porphyry copper deposit, Northern Chile, consists of two major intrusions, the 290 Ma Zaldívar, and the more recent Miocene (38.7 Ma) Llamo porphyry. Five types of inclusions have been identified in quartz phenocrysts from Llamo porphyry, including melt inclusions (M), and four types of fluid inclusions, called MS (multi solids), B (brines), G (vapor-rich) and W (aqueous), respectively.Melt remnants, well preserved as M-inclusions, homogenize around 1000 °C. They show a rhyolitic composition, comparable to the most evolved acidic rhyolitic end member found elsewhere in the regional magmatism and to worldwide volcanic rhyolitic glass. High silica content in some inclusions can, however, be due to partial remelting of the quartz host during the heating run. Copper content in the same inclusions ranges between 0.03 and 0.57 wt.%, with an average concentration of 0.10 wt.%, suggesting a major magmatic source for the copper (orthomagmatic model).MS inclusions, which contain a number of solids at room temperature, mostly H₂O-bearing phases (system NaCl–KCl–((Fe, Mg, Cu)Cl)–H₂O, average salinity 70 wt.% NaCl equiv.), homogenize at magmatic temperatures (around 1000 °C). They represent the first fluids to have exsolved from the magma at depth, at a pressure of about 2 kbar. Their high homogenization temperature, comparable to values measured for melt inclusions (1000 to 1050 °C), may indicate trapping of MS and M inclusions in host phenocrysts from an immiscible mixture of silicate melt and highly saline fluids expelled from the magma during the early stage of quartz crystallization.The data indicate a magmatic origin for copper, as well as extremely high melt temperatures. These features are interpreted by magmatic differentiation of mantle-derived primitive melts, corresponding to major changes in the tectonic regime of the Andean margin, which occurred in Miocene times.