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1.
The Darreh-Zar porphyry copper deposit is associated with a quartz monzonitic–granodioritic–porphyritic stock hosted by an Eocene volcanic sedimentary complex in which magmatic hydrothermal fluids were introduced and formed veins and alteration. Within the deepest quartz-rich and chalcopyrite-poor group A veins, LVHS2 inclusions trapped high salinity, high temperature aqueous fluids exsolved directly from a relatively shallow magma (0.5 kbar). These late fluids were enriched in NaCl and reached halite saturation as a result of the low pressure of magma crystallization and fluid exsolution. These fluids extracted Cu from the crystallizing melt and transported it to the hydrothermal system. As a result of ascent, the temperature and pressure of these fluids decreased from 600 to 415 °C, and approximately 500–315 bars. At these conditions, K-feldspar and biotite were stabilized. Type A veins were formed at a depth of ∼1.2 km under conditions of lithostatic pressure and abrupt cooling. Upon cooling and decompressing, the fluid intersected with the liquid–vapor field resulting in separation of immiscible liquid and vapor. This stage was recorded by formation of LVHS1, LVHS3 and VL inclusions. These immiscible fluids formed chalcopyrite–pyrite–quartz veins with sericitic alteration envelopes (B veins) under the lithostatic–hydrostatic pressure regime at temperatures between 415 and 355 °C at 1.3 km below the paleowater table. As the fluids ascended, copper contents decreased and these fluids were diluted by mixing with the low salinity-external fluid. Therefore, pyrite-dominated quartz veins were formed in purely hydrostatic conditions in which pressure decreased from 125 bars to 54 bars and temperature decreased from 355 to 298 °C. During the magmatic-hydrothermal evolution, the composition and P–T regime changed drastically and caused various types of veins and alterations. The abundance of chalcopyrite precipitation in group B veins suggests that boiling and cooling were important factors in copper mineralization in Darreh-Zar.  相似文献   

2.
The Guelb Moghrein copper–gold deposit in the Islamic Republic of Mauritania reopened in 2006 and has produced copper concentrate and gold since then. The deposit is hosted in Neoarchaean–Palaeoproterozoic Fe–Mg carbonate-dominated metamorphic rocks interpreted as carbonate-facies iron formation. It forms tabular orebodies controlled by shear zones in the hanging wall and footwall of this meta-iron formation. Copper and gold are hosted in a complex sulfide ore in tectonic breccia replacing Fe–Mg carbonate and magnetite. Hydrothermal monazite dates the mineralization at 2492 ± 9 Ma. Two types of aqueous fluid inclusions suggest fluid mixing at 0.75–1.80 kbar and ~ 410 °C as the mineralization and precipitation mechanism, which is temporally coincident with regional retrograde metamorphism at 410 ± 30 °C (garnet-biotite). Distal alteration zones are enriched in K, Rb and Cu, whereas orebodies are depleted in K, Rb, Sr and Ba. The copper–gold mineralization at Guelb Moghrein formed during retrograde shearing in metamorphic rocks and contemporaneous hydrothermal alteration. The stable isotope signature of alteration and ore minerals suggest an external crustal fluid source. Fluids were focused in the reactive and competent meta-iron formation. Potassium alteration, magnetite and copper–gold mineralization suggest an IOCG mineral system akin similar deposits in Australia and Brazil.  相似文献   

3.
In the San Marcos ranges of Cuatrociénegas, NE Mexico, several sediment-hosted copper deposits occur within the boundary between the Coahuila Block, a basement high mostly granitic in composition and Late Paleozoic to Triassic in age, and the Mesozoic Sabinas rift basin. This boundary is outlined by the regional-scale synsedimentary San Marcos Fault. At the basin scale, the copper mineralization occurs at the top of a ～1000 m thick red-bed succession (San Marcos Formation, Berrisian), a few meters below a conformable, transitional contact with micritic limestones (Cupido Formation, Hauterivian to Aptian). It consists of successive decimeter-thick roughly stratiform copper-rich horizons placed just above the red-beds, in a transitional unit of carbonaceous grey-beds grading to micritic limestones. The host rocks are fine- to medium-grained arkoses, with poorly sorted and subangular to subrounded grains. The detrital grains are cemented by quartz and minor calcite; besides, late iron oxide grain-coating cement occurs at the footwall unmineralized red-beds. The source area of the sediments, indicated by their modal composition, is an uplifted basement. The contents of SiO2 (40.70–87.50 wt.%), Al2O3 (5.91–22.00 wt.%), K2O (3.68–12.50 wt.%), Na2O (0.03–2.03 wt.%) and CaO (0.09–3.78 wt.%) are within the ranges expected for arkoses. Major oxide ratios indicate that the sedimentary-tectonic setting was a passive margin.The outcropping copper mineralization essentially consists in a supergene assemblage of chrysocolla, malachite and azurite. All that remains of the primary mineralization are micron-sized chalcocite grains shielded by quartz cement. In addition, pyrite subhedral grains occur scattered throughout the copper-mineralized horizons. In these weathered orebodies copper contents range between 4.24 and 7.72 wt.%, silver between 5 and 92 ppm, and cobalt from 8 to 91 ppm. Microthermometric measurements of fluid inclusions in quartz and calcite crystals from footwall barren veinlets gave temperatures of homogenization between 98 °C and 165 °C, and ice-melting temperatures between ?42.5 °C and ?26.1 °C.The primary copper mineralization formed during the early diagenesis, contemporary with the active life of the Sabinas Basin. The mineralizing fluids were dense, near neutral, moderately oxidized brines that originally formed from seawater that, driven by gravity, infiltrated to the deepest parts of the basin and dissolved evaporites. As a result, they became hydrothermal fluids of moderate temperature capable of leaching high amounts of copper. The source of this metal could be mafic detrital grains and iron oxides of the underlying Jurassic and Lower Cretaceous red-beds. Copper precipitation took place when the brines passed through the redox boundary marked by the transition from red- to grey-beds. The upward movement of the brines was promoted by a high heat flow that allowed their convective circulation and their ascent along the synsedimentary San Marcos Fault.  相似文献   

4.
The Huangshaping Pb–Zn–W–Mo polymetallic deposit, located in southern Hunan Province, China, is one of the largest deposits in the region and is unique for its metals combination of Pb–Zn–W–Mo and the occurrence of significant reserves of all these metals. The deposit contains disseminated scheelite and molybdenite within a skarn zone located between Jurassic granitoids and Carboniferous sedimentary carbonate, and sulfide ores located within distal carbonate-hosted stratiform orebodies. The metals and fluids that formed the W–Mo mineralization were derived from granitoids, as indicated by their close spatial and temporal relationships. However, the source of the Pb–Zn mineralization in this deposit remains controversial.Here, we present new sulfur, lead, and strontium isotope data of sulfide minerals (pyrrhotite, sphalerite, galena, and pyrite) from the Pb–Zn mineralization within the deposit, and these data are compared with those of granitoids and sedimentary carbonate in the Huangshaping deposit, thereby providing insights into the genesis of the Pb–Zn mineralization. These data indicate that the sulfide ores from deep levels in the Huangshaping deposit have lower and more consistent δ34S values (− 96 m level: + 4.4‰ to + 6.6‰, n = 13) than sulfides within the shallow part of the deposit (20 m level: + 8.3‰ to + 16.3‰, n = 19). The δ34S values of deep sulfides are compositionally similar to those of magmatic sulfur within southern Hunan Province, whereas the shallower sulfides most likely contain reduced sulfur derived from evaporite sediments. The sulfide ores in the Huangshaping deposit have initial 87Sr/86Sr ratios (0.707662–0.709846) that lie between the values of granitoids (0.709654–0.718271) and sedimentary carbonate (0.707484–0.708034) in the Huangshaping deposit, but the ratios decreased with time, indicating that the ore-forming fluids were a combination of magmatic and formation-derived fluids, with the influence of the latter increasing over time. The lead isotopic compositions of sulfide ores do not correlate with sulfide type and define a linear trend in a 207Pb/204Pb vs. 206Pb/204Pb diagram that is distinct from the composition of the disseminated pyrite within sedimentary carbonates and granitoids in the Huangshaping deposit, but is similar to the lead isotopic composition of sulfides within coeval skarn Pb–Zn deposits in southern Hunan Province. In addition, the sulfide ores have old signatures with relative high 207Pb/206Pb ratios, suggesting that the underlying Paleoproterozoic basement within southern Hunan Province may be the source of metals within the Huangshaping deposit.The isotope geochemistry of sulfide ores in the Huangshaping deposit shows a remarkable mixed source of sulfur and ore-forming fluids, and the metals were derived from the basement. These features are not found in representative skarn-type Pb–Zn mineralization located elsewhere. The ore-forming elements (S, Pb, and Zn) from the granitoids made an insignificant contribution to sulfide precipitation in this deposit. However, the emplacement of granitoids did provide large amounts of heat and fluids to the hydrothermal system in this area and extracted metals from the basement rocks, indicating that the Jurassic magmatism associated with the Huangshaping deposit was crucial to the Pb–Zn mineralization.  相似文献   

5.
The Dabu Cu-Mo porphyry deposit is situated in the southern part of the Lhasa terrane within the post-collisional Gangdese porphyry copper belt (GPCB). It is one of several deposits that include the Qulong and Zhunuo porphyry deposits. The processes responsible for ore formation in the Dabu deposit can be divided into three stages of veining: stage I, quartz–K-feldspar (biotite) ± chalcopyrite ± pyrite, stage II, quartz–molybdenite ± pyrite ± chalcopyrite, and stage III, quartz–pyrite ± molybdenite. Three types of fluid inclusions (FIs) are present: liquid-rich two-phase (L-type), vapor-rich two-phase (V-type), and solid bearing multi-phase (S-type) inclusions. The homogenization temperatures for the FIs from stages I to III are in the ranges of 272–475 °C, 244–486 °C, and 299–399 °C, and their salinities vary from 2.1 to 49.1, 1.1 to 55.8, and 2.9 to 18.0 wt% NaCl equiv., respectively. The coexistence of S-type, V-type and L-type FIs in quartz of stage I and II with similar homogenization temperatures but contrasting salinities, indicate that fluid boiling is the major factor controlling metal precipitation in the Dabu deposit. The ore-forming fluids of this deposit are characterized by high temperature and high salinity, and they belong to a H2O–NaCl magmatic–hydrothermal system. The H–O–S–Pb isotopic compositions indicate that the ore metals and fluids came primarily from a magmatic source linked to Miocene intrusions characterized by high Sr/Y ratios, similar to other porphyry deposits in the GPCB. The fluids forming the Dabu deposit were rich in Na and Cl, derived from metamorphic dehydration of subducted oceanic slab through which NaCl-brine or seawater had percolated. The inheritance of ancient subduction-associated arc chemistry, without shallow level crustal assimilation and/or input of the meteoric water, was responsible for the generation of fertile magma, as well as CO2-poor and halite-bearing FIs associated with post-collisional porphyry deposits. The estimated mineralization depths of Qulong, Dabu and Zhunuo deposits are 1.6–4.3 km, 0.5–3.4 km and 0.2–3.0 km, respectively, displaying a gradual decrease from eastern to western Gangdese. Deep ore-forming processes accounted for the generation of giant-sized Qulong deposit, because the exsolution of aqueous fluids with large fraction of water and chlorine in deep or high pressure systems can extract more copper from melts than those formed in shallow systems. However, the formation of small-sized Dabu deposit can be explained by a single magmatic event without additional replenishment of S, metal, or thermal energy. In addition, the ore-forming conditions of porphyry Cu–Mo deposits in GPCB are comparable to those of porphyry Cu ± Au ± Mo deposits formed in oceanic subduction-related continental or island arcs, but differ from those of porphyry Mo deposit formed in the Dabie-Qinling collisional orogens. The depth of formation of the mineralization and features of primary magma source are two major controls on the metal types and ore-fluid compositions of these porphyry deposits.  相似文献   

6.
The several-hundred-m-thick Miocene Upper Red Formation in northwestern Iran hosts stratiform and fault-controlled copper mineralization. Copper enrichment in the percent range occurs in dm-thick carbonaceous sandstone and shale units within the clastic redbed sequence and consists of fine-grained disseminated copper sulfides (chalcopyrite, bornite, chalcocite) and supergene alteration minerals (covellite, malachite and azurite). The copper mineralization formed after calcite cementation of the primary rock permeability. Copper sulfides occur mainly as replacement of diagenetic pyrite, which, in turn, replaced organic matter. Electron microprobe analysis on bornite, chalcocite and covellite identifies elevated silver contents in these minerals (up to 0.12, 0.72 and 1.21 wt%, respectively), whereas chalcopyrite and pyrite have only trace amounts of silver (<0.26 and 0.06 wt%, respectively). Microthermometric data on fluid inclusions in authigenic quartz and calcite indicate that the Cu mineralization is related to a diagenetic fluid of moderate-to low temperature (Th = 96–160 °C) but high salinity (25–38 wt% CaCl2 equiv.). The range of δ34S in pyrite is −41.9 to −16.4‰ (average −31.4‰), where framboidal pyrite shows the most negative values between −41.9 and −31.8‰, and fine-grained pyrite has relatively heavier δ34S values (−29.2 to −16.4‰), consistent with a bacteriogenic derivation of the sulfur. The Cu-sulfides (chalcopyrite, bornite and chalcocite) show slightly heavier values from −14.6 to −9.0‰, and their sulfur sources may be both the precursor pyrite-S and the bacterial reduction of sulfate-bearing basinal brines. Carbonates related to the ore stage show isotopically light values of δ13CV-PDB from −8.2 to −5.1‰ and δ18OV-PDB from −10.3 to −7.2‰, indicating a mixed source of oxidation of organic carbon (ca. −20‰) and HCO3− from seawater/porewater (ca. 0‰). The copper mineralization is mainly controlled by organic matter content and paleopermeability (intragranular space to large fracture patterns), enhanced by feldspar and calcite dissolution. The Cheshmeh-Konan deposit can be classified as a redbed-type sediment-hosted stratiform copper (SSC) deposit.  相似文献   

7.
The Jabali Zn–Pb–Ag deposit is located about 110 km east of Sana'a, the capital of Yemen, along the western border of the Marib-Al-Jawf/Sab'atayn basin. The economic mineralization at Jabali is a nonsulfide deposit, consisting of 8.7 million tons at an average grade of 9.2% zinc, derived from the oxidation of primary sulfides. The rock hosting both primary and secondary ores is a strongly dolomitized carbonate platform limestone of the Jurassic Shuqra Formation (Amran Group). The primary sulfides consist of sphalerite, galena and pyrite/marcasite. Smithsonite is the most abundant economic mineral in the secondary deposit, and is associated with minor hydrozincite, hemimorphite, acanthite and greenockite. Smithsonite occurs as two main generations: smithsonite 1, which replaces both host dolomite and sphalerite, and smithsonite 2, occurring as concretions and vein fillings in the host rock. At the boundary between smithsonite 1 and host dolomite, the latter is widely replaced by broad, irregular bands of Zn-bearing dolomite, where Zn has substituted for Mg. The secondary mineralization evolved through different stages: 1) alteration of original sulfides (sphalerite, pyrite and galena), and release of metals in acid solutions; 2) alteration of dolomite host rock and formation of Zn-bearing dolomite; 3) partial dissolution of dolomite by metal-carrying acid fluids and replacement of dolomite and Zn-bearing dolomite by a first smithsonite phase (smithsonite 1). To this stage also belong the direct replacement of sphalerite and galena by secondary minerals (smithsonite and cerussite); 4) precipitation of a later smithsonite phase (smithsonite 2) in veins and cavities, together with Ag- and Cd-sulfides.The δ18O composition of Jabali smithsonite is generally lower than in other known supergene smithsonites, whereas the carbon isotope composition is in the same range of the negative δ13C values recorded in most supergene nonsulfide ores. Considering that the groundwaters and paleo-groundwaters in this area of Yemen have negative δ18O values, it can be assumed that the Jabali smithsonite precipitated in different stages from a combination of fluids, possibly consisting of local groundwaters variably mixed with low-temperature hydrothermal waters. The carbon isotope composition is interpreted as a result of mixing between carbon from host rock carbonates and soil/atmospheric CO2.The most favorable setting for the development of the Jabali secondary deposit could be placed in the early Miocene (~ 17 Ma), when supergene weathering was favored by major uplift and exhumation resulting from the main phase of Red Sea extension. Low-temperature hydrothermal fluids may have also circulated at the same time, through the magmatically-induced geothermal activity in the area.  相似文献   

8.
The Wangu gold deposit in northeastern Hunan, South China, is one of many structurally controlled gold deposits in the Jiangnan Orogen. The host rocks (slates of the Lengjiaxi Group) are of Neoproterozoic age, but the area is characterized by a number of Late Jurassic–Cretaceous granites and NE-trending faults. The timing of mineralization, tectonic setting and ore genesis of this deposit and many similar deposits in the Jiangnan Orogen are not well understood. The orebodies in the Wangu deposit include quartz veins and altered slates and breccias, and are controlled by WNW-trending faults. The principal ore minerals are arsenopyrite and pyrite, and the major gangue minerals are quartz and calcite. Alteration is developed around the auriferous veins, including silicification, pyritic, arsenopyritic and carbonate alterations. Field work and thin section observations indicate that the hydrothermal processes related to the Wangu gold mineralization can be divided into five stages: 1) quartz, 2) scheelite–quartz, 3) arsenopyrite–pyrite–quartz, 4) poly-sulfides–quartz, and, 5) quartz–calcite. The Lianyunshan S-type granite, which is in an emplacement contact with the NE-trending Changsha-Pingjiang fracture zone, has a zircon LA-ICPMS U–Pb age of 142 ± 2 Ma. The Dayan gold occurrence in the Changsha-Pingjiang fracture zone, which shares similar mineral assemblages with the Wangu deposit, is crosscut by a silicified rock that contains muscovite with a ca. 130 Ma 40Ar–39Ar age. The gold mineralization age of the Wangu deposit is thus confined between 142 Ma and 130 Ma. This age of mineralization suggests that the deposit was formed simultaneously with or subsequently to the development of NE-trending extensional faults, the emplacement of Late Jurassic–Cretaceous granites and the formation of Cretaceous basins filled with red-bed clastic rocks in northeastern Hunan, which forms part of the Basin and Range-like province in South China. EMPA analysis shows that the average As content in arsenopyrite is 28.7 atom %, and the mineralization temperature of the arsenopyrite–pyrite–quartz stage is estimated to be 245 ± 20 °C from arsenopyrite thermometry. The high but variable Au/As molar ratios (>0.02) of pyrite suggest that there are nanoparticles of native Au in the sulfides. An integration of S–Pb–H–O–He–Ar isotope systematics suggests that the ore fluids are mainly metamorphic fluids originated from host rocks, possibly driven by hydraulic potential gradient created by reactivation of the WNW-trending faults initially formed in Paleozoic, with possible involvement of magmatic and mantle components channeled through regional fault networks. The Wangu gold deposit shares many geological and geochemical similarities as well as differences with typical orogenic, epithermal and Carlin-type gold deposits, and may be better classified as an “intracontinental reactivation” type as proposed for many other gold deposits in the Jiangnan Orogen.  相似文献   

9.
We present results of isotope-geochemical study of the Ermakovka F-Be deposit, including data on the oxygen and carbon isotope compositions in dolomite and calcite marbles and in carbonates accompanying skarns, of early and late stages of ore formation and of post-ore parageneses. To elucidate the sources of fluids participated in the ore formation, we calculated the oxygen isotope composition in water and the hydrogen isotope composition in hydroxyl-containing minerals. Phlogopite in marbleized dolomites, vesuvianite and amphibole in skarns, eudidimite and bertrandite in ore parageneses, and bavenite formed during post-ore processes are analyzed. Most of the ore-stage minerals are depleted in heavy oxygen. Their 518O values are lower than 5-6%c (SMOW). Oxygen in carbonate minerals of the initial stage (dolomite and bastnaesite) is heavier (1.3-4.9%c) than that in calcite (+ 2 to -3.7%c). The 518O values of water in equilibrium both with carbonate and with silicate minerals (-4 to -14%c) suggest the contribution of meteoric water to the mineral formation. A magmatic fluid (518O from + 6 to + 9%c) participated in the skarn formation at the initial stage, and a meteoric fluid, at the final stage (518O from -1 to -9%c). A meteoric source is confirmed by the depleted hydrogen isotope composition in minerals (5D from -119 to -192%c).  相似文献   

10.
Stratabound massive sulfide deposits are widespread along the Middle-Lower Yangtze Metallogenic Belt (MLYMB) and serve as an important copper producer in China. Two contrasting genetic models have been proposed, interpreting the stratabound massive sulfide deposits as a Carboniferous SEDEX protore overprinted by Cretaceous magmatic-hydrothermal system or an Early Cretaceous carbonate replacement deposit. These two contrasting models have been applied to the Xinqiao stratabound Cu-Au sulfide deposit, which is dominated by massive sulfide ores hosted in marine carbonates of the Carboniferous Chuanshan and Huanglong Formations, with minor Cu-Au skarn ores localized in the contact zone between the Cretaceous diorite Jitou stock and the Carboniferous carbonate rocks. New SIMS zircon U-Pb dating suggests that the Jitou stock formed at 138.5 ± 1.1 Ma (2σ, MSWD = 0.6). Pyrite Re-Os dating yields an imprecise date of 142 ± 47 Ma (2σ, MSWD = 7.8). The geochronological data thus constrain the mineralization of the Xinqiao deposit at Early Cretaceous.Fluid inclusions in prograde skarn diopside have homogenization temperatures of 450–600 °C and calculated salinities of 13–58 wt.% NaCl equiv. Quartz from the stratabound ores and pyrite-quartz vein networks beneath the stratabound ores have homogenization temperatures of 290–360 and 200–300 °C, with calculated salinities of 5–12 and 2–10 wt.% NaCl equiv., respectively. Quartz from the skarn ores and veins beneath the stratabound ores have δ18O values of 12.32 ± 0.55 (2 SD, n = 22) and 15.57 ± 1.92‰ (2 SD, n = 60), respectively, corresponding to calculated δ18O values of 6.22 ± 1.59 (2σ) and 6.81 ± 2.76‰ (2σ) for the equilibrated ore-forming fluids. The fluid inclusion and oxygen isotope data thus support a magmatic-hydrothermal origin rather than a SEDEX system for the stratabound ores, with the hydrothermal fluids most likely being derived from the Jitou stock or associated concealed intrusion. Results from this study have broad implications for the genesis and exploration of other stratabound massive sulfide deposits along the MLYMB.  相似文献   

11.
The Bayan Obo Fe-REE-Nb deposit in northern China is the world's largest light REE deposit, and also contains considerable amounts of iron and niobium metals. Although there are numerous studies on the REE mineralization, the origin of the Fe mineralization is not well known. Laser ablation (LA) ICP-MS is used to obtain trace elements of Fe oxides in order to better understand the process involved in the formation of magnetite and hematite associated with the formation of the giant REE deposit. There are banded, disseminated and massive Fe ores with variable amounts of magnetite and hematite at Bayan Obo. Magnetite and hematite from the same ores show similar REE patterns and have similar Mg, Ti, V, Mn, Co, Ni, Zn, Ga, Sn, and Ba contents, indicating a similar origin. Magnetite grains from the banded ores have Al + Mn and Ti + V contents similar to those of banded iron formations (BIF), whereas those from the disseminated and massive ores have Al + Mn and Ti + V contents similar to those of skarn deposits and other types of magmatic-hydrothermal deposits. Magnetite grains from the banded ores with a major gangue mineral of barite have the highest REE contents and show slight moderate REE enrichment, whereas those from other types of ores show light REE enrichment, indicating two stages of REE mineralization associated with Fe mineralization. The Bayan Obo deposit had multiple sources for Fe and REEs. It is likely that sedimentary carbonates provided original REEs and were metasomatized by REE-rich hydrothermal fluids to form the giant REE deposit.  相似文献   

12.
The Upper Cretaceous Nakhlak epigenetic vein-type Pb(Ag) deposit is located 55 km northeast of the town of Anarak in Isfahan Province, Iran. The deposit contains 7 Mt of galena-barite ore with an average grade of 8.33% Pb, 0.38% Zn, and 72 ppm Ag. The ore mineralization occurs as stratabound, epigenetic, steeply dipping, east-west–trending veins in faulted- or fracture-controlled Upper Cretaceous Sadar carbonates. Galena and barite are the primary minerals. Minor sphalerite, tennantite-tetrahedrite, pyrite, and chalcopyrite occur as inclusions in galena. Cerussite with minor amounts of anglesite and plattnerite formed in the oxidized supergene zone. The ore and ore-related minerals were deposited in the hydrothermally dolomitized carbonate host rock containing saddle-shaped dolomite. Geochemically, the dolomitized carbonate host rocks are enriched in MgO, Fe2O3, MnO, Pb, Zn, and Ba, but depleted in CaO. The galena concentrate contains high values of Ag (932 ppm), Sb (342 ppm), Cu (422 ppm), As (91 ppm), and Zn (296 ppm); the presence of these trace elements indicates a low-temperature type of galena mineralization. This interpretation is corroborated by fluid inclusions containing 12.98 wt.% NaCl equivalent salinity; the inclusions homogenize at the low temperature of about 152.1 °C. The similarity between δ34S(V-CDT) values in Nakhlak barite and Permian–Triassic δ34S marine sulfate values indicates that the Nakhlak sulfur was probably provided from evaporates of Permian–Triassic age. The δ34S(V-CDT) values of galena and barite samples occupy the ranges of − 1.04‰ to + 8.62‰ and + 10.95‰ to + 13.71‰, respectively, and are similar to Mississippi Valley–type (MVT) deposits. The low-temperature basinal fluids, evaporate-originated sulfur, and fault- or fracture-controlled galena-rich veins in the Nakhlak deposit resemble the type of geological features documented in Pb-rich MVT deposits.  相似文献   

13.
The Mokrsko-West deposit is unique among European Variscan gold deposits from the points of view of both the structure (an approx. 200 m thick complex of sheeted, several mm-thick, densely spaced quartz veins) and the economic viability (gold reserves of about 100 t). The deposit is hosted mainly by tonalite of the calc-alkaline Sázava tonalite suite (ca. 354 Ma) of the Central Bohemian Plutonic Complex. Mineralization is characterized by quartz-dominated gangue, no visible hydrothermal alteration, low sulfide content, high fineness native gold accompanied by maldonite, aurostibite, native bismuth and numerous Bi–Te–(S) phases. Five mineralogical stages are described in great detail. Arsenopyrite and chlorite thermometers, mineral phase stabilities and published isotope and fluid inclusion data are used to reconstruct the temperature and compositional evolution of the system. The role of liquid bismuth in the sequestration of gold is also discussed.The deposit shares the features of both orogenic gold (ORG) and intrusion-related gold (IRG) deposits. The IRG model is advocated by close spatial association between the ore zone and the tonalite host-intrusion, by the absence/scarcity of hydrothermal alteration, by the Au–Bi–Te–As elemental association and by marked thermal gradients from the early to late mineralization stages. The ORG model is advocated by an approx. 15–10 Ma gap between the intrusion of the tonalite-host and the ore formation, by isotope and geochemical evidence for a key role of metamorphic fluids in the mobilization and transfer of many elements/species (inclusive S and Au). The apparently ambiguous classification of the deposit can most probably be attributed to deposit formation at a depth of ≥ 9 km and to setting of the deposit at/inside a large-scale plutonic complex with multiple and prolonged tectonic and intrusive activity.  相似文献   

14.
The Laowan metallogenic belt in China is an important metallogenic belt within the Tongbai orogenic belt, and contains the medium-sized Laowan and Shangshanghe gold deposits, the small Huangzhuyuan lead–zinc–silver–gold deposit and some gold and Cu–Pb occurrences. These deposits are hosted in Mesoproterozoic plagioclase amphibolite (or schist) and mica-quartz schist. The gold ores are mainly quartz veins and veinlets and disseminated altered ores. Subordinate ore types include massive sulfides and breccias. The Laowan gold deposit is characterized by three right-stepping en-echelon fracture-controlled alteration zones that dip gently to the south and includes disseminated, sheeted and stockwork ores. These lodes were formed by the interaction of ore-forming fluid with foliated-to laminated cataclasite within the transpressional faults. The Shangshanghe gold deposit is characterized by parallel ore lodes that dip steeply to the north, and includes quartz veins and breccias in addition to ores in altered wallrocks. These lodes were formed by focusing of fluids into transtensional faults. These ore controlling faults displaced early barren quartz veins 10 m horizontally with a dextral sense of motion. The ore-hosting structures at the Laowan and Shangshanghe deposits correspond to the P and R-type shears of a brittle dextral strike-slip fault system, respectively, which make angles of about 15° and − 15° to the Laowan and Songpa boundary faults. The ore-controlling fault system post-dated formation of a ductile shear zone, and peak regional metamorphism. This precludes a genetic relationship between hydrothermal mineralization and regional metamorphism and ductile shear deformation. These gold deposits are not typical orogenic gold deposits. The metallogenic belt displays district-scale-zoning of Mo → Cu–Pb–Zn–Ag → Au relative to Songpa granite porphyry dike zone, suggesting the mineralization may be closely related to the granite porphyry. Measured δ34S of sulfides and δ18O and δD of fluid inclusion waters in auriferous quartz also are consistent with a magmatic source for sulfur and ore fluids. The similarity of Pb isotope ratios between the ores and Yanshanian granitoids suggests a similar source. As the age (139 ± 3 Ma) of granite porphyry obtained by zircon U–Pb isotope overlaps the mineralization age (138 ± 1 Ma: Zhang et al., 2008a), the gold and polymetallic metallogenesis of the Laowan gold belt has close spatial, temporal and possibly genetic relationships with Yanshanian high level magmatism.  相似文献   

15.
The Hattu schist belt is located in the western part of the Archaean Karelian domain of the Fennoscandian Shield. The orogenic gold deposits with Au–Bi–Te geochemical signatures are hosted by NE–SW, N–S and NW–SE oriented shear zones that deform 2.76–2.73 Ga volcanic and sedimentary sequences, as well as 2.75–2.72 Ga tonalite–granodiorite intrusions and diverse felsic porphyry dykes. Mo–W mineralization is also present in some tonalite intrusions, both separate from, and associated with Au mineralization. Somewhat younger, unmineralized leucogranite intrusions (2.70 Ga) also intrude the belt. Lower amphibolite facies peak metamorphism at 3–5 kbar pressures and at 500–600 °C temperatures affected the belt at around 2.70 Ga and post-date hydrothermal alteration and ore formation. In this study, we investigated the potential influence of magmatic-hydrothermal processes on the formation of orogenic gold deposits on the basis of multiple stable isotope (B, S, Cu) studies of tourmaline and sulphide minerals by application of in situ SIMS and LA ICP MS analytical techniques.Crystal chemistry of tourmaline from a Mo–W mineralization hosted by a tonalite intrusion in the Hattu schist belt is characterized by Fe3 +–Al3 +-substitution indicating relatively oxidizing conditions of hydrothermal processes. The range of δ11B data for this kind of tourmaline is from − 17.2‰ to − 12.2‰. The hydrothermal tourmaline from felsic porphyry dyke swith gold mineralization has similar crystal chemistry (e.g. dravite–povondraite compositional trend with Fe3 +–Al3 + substitution) and δ11B values between − 19.0‰ and − 9.6‰. The uvite–foitite compositional trend and δ11B ‰ values between − 24.1% and − 13.6% characterize metasomatic–hydrothermal tourmaline from the metasediment-hosted gold deposits. Composition of hydrothermal vein-filling and disseminated tourmaline from the gold-bearing shear zones in metavolcanic rocks is transitional between the felsic intrusion and metasedimentary rock hosted hydrothermal tourmaline but the range of average boron isotope data is essentially identical with that of the metasediment-hosted tourmaline. Rock-forming (magmatic) tourmaline from leucogranite has δ11B values between − 14.5‰ and − 10.8‰ and the major element composition is similar to that of the metasediment-hosted tourmaline.The range of δ34SVCDT values measured in pyrite, chalcopyrite and pyrrhotite is from − 9.1 to + 8.5‰, which falls within the typical range of sulphur isotope data for Archaean orogenic gold deposits. In the Hattu schist belt, positive δ34SVCDT values characterize metasediment-hosted gold ores with sulphide parageneses dominated by pyrrhotite and arsenopyrite. The δ34SVCDT values are both positive and negative in ore mineral parageneses within felsic intrusive rocks in which variable amounts of pyrrhotite are associated with pyrite. Purely negative values were only recorded from the pyrite-dominated gold mineralization within metavolcanic units. Therefore the shift of δ34SVCDT values to the negative values reflects precipitation of sulphide minerals from relatively oxidizing fluids. The range of measured δ65CuNBS978 values from chalcopyrite is from − 1.11 to 1.19‰. Positive values are common for mineralization in felsic intrusive rocks and negative values are more typical for deposits confined to metasedimentary rocks. Positive and negative δ65CuNBS978 values occur in the ores hosted by metavolcanic rocks. There is no correlation between sulphur and copper isotope data obtained in the same chalcopyrite grains.Evaluation of sulphur and boron isotope data together and comparisons with other Archaean orogenic gold provinces supports the hypothesis that the metasedimentary rocks were the major sources of sulphur and boron in the orogenic gold deposits in the Hattu schist belt. Variations in major element and boron isotope compositions in tourmaline, as well as in the δ34SVCDT values in sulphide minerals are attributed to localized involvement of magmatic fluids in the hydrothermal processes. The results of copper isotope studies indicate that local sources of copper in orogenic gold deposits may potentially be recognized if the original, distinct signatures of the sources have not been homogenized by widespread interaction of fluids with a large variety of rocks and provided that local chemical variations have been too small to trigger changes in the oxidation state of copper during hydrothermal processes.  相似文献   

16.
The Wulasigou Cu deposit occurs as veins controlled by a NW-trending structure in a Devonian volcano-sedimentary basin of the Altay orogenic belt, Xinjiang, China. Igneous and sedimentary rocks exposed in the area have undergone greenschist-facies metamorphism. The ore-forming process can be divided into early, middle, and late stages, represented by, respectively, pyrite-quartz, polymetallic sulfide-quartz, and carbonate–quartz veins, veinlets, and/or replacement bodies. The early veins were deformed and brecciated during a compressional or transpressional event. The middle-stage veinlets filled fractures in the early-stage vein and alteration assemblages, and are undeformed, suggesting a tensional shear setting. The late-stage veinlets are mainly open-space fissure fillings that cut veins and replacement bodies formed in the earlier stages.Four types of fluid inclusions (FIs), including aqueous (W-type), mixed carbonic-aqueous (M-type), purely carbonic (C-type) and daughter mineral-bearing (S-type), have been identified in copper-related quartz and calcite from the Wulasigou deposit. The early-stage quartz contains M- and W-type primary FIs that completely homogenized at temperatures of 322–412 °C with low salinities of 0.9–6.5 wt.% NaCl equiv. In contrast, the late-stage quartz or calcite contains only the W-type FIs with homogenization temperatures of 101–234 °C, and salinities of 0.9–2.9 wt.% NaCl equiv. This indicates that the metallogenic system evolved from CO2-rich, metamorphic to CO2-poor, through input of meteoric fluids. All four types of FIs can only be observed in the middle-stage minerals, where they show evidence of vein formation during an episode of fluid immiscibility. These FIs homogenized at temperatures ranging mainly from 230 to 347 °C, with salinities clustering 2.7–10.2 wt.% NaCl equiv for the W-, M- and C-types, and 34.7–38.2 wt.% NaCl equiv for the S-type, respectively. The metal precipitation resulted from a decrease in copper solubility during the fluid immiscibility episode. The estimated trapping pressures for the middle-stage fluids are 1.55–3.55 kbar, suggesting an alternating lithostatic-hydrostatic fluid-system, controlled by fault-valve activity at a depth of 13–15.5 km.Muscovite separates from the middle-stage polymetallic-quartz veinlets yield a well-defined 40Ar/39Ar isotopic plateau age of 219.41 ± 2.10 Ma, and an 39Ar/36Ar - 40Ar/36Ar isochron age of 219.73 ± 2.17 Ma. This age postdates the final Paleo-Asia Ocean closure (at ca. 250 Ma) by about 30 Ma, and indicates that the Cu mineralization at Wulasigou has occurred in the Triassic continental collision setting. Hence, the Wulasigou Cu deposit may be the first example of orogenic lode Cu deposits formed in accretionary orogeny or continental collision.  相似文献   

17.
The Tongjing Cu–Au deposit is a medium-sized deposit within the Ningwu volcanic basin, east China, and is hosted by Cretaceous volcanic rocks of the Dawangshan and Niangniangshan Formations. The veined and lenticular Cu–Au orebodies are spatially and temporally related to the volcanic and subvolcanic rocks of the Niangniangshan Formation in the ore district. The wall-rock alteration is dominated by silicification, siderite alteration, carbonation, sericitization, chloritization, and kaolinization. On the basis of field evidence and petrographic observations, two stages of mineralization are recognized: (1) a siderite–quartz–sulfide stage (Stage 1) associated with the formation of chalcopyrite and pyrite in a quartz and siderite gangue; and (2) a quartz–bornite stage (Stage 2) cutting the Stage 1 phases. Stage 1 is the main mineralization stage. Quartz that formed in Stage 1 has δ18OH2O values of − 4.3‰ to 3.5‰ with δD values of fluid inclusion waters of − 97.1‰ to − 49.9‰, indicating that the ore-forming fluids were derived from early magmatic fluids and may have experienced oxygen isotopic exchange with meteoric water during Stage 1 mineralization.LA–MC–ICP–MS zircon U–Pb dating of the mineralization-related nosean-bearing phonolite and nosean-bearing phonolitic brecciated tuff at Tongjing yields ages of 129.8 ± 0.5 Ma and 128.9 ± 1.1 Ma, respectively. These results are interpreted as the crystallization age of the volcanic rocks of the Niangniangshan Formation. A hydrothermal sericite sample associated with Cu–Au mineralization at Tongjing yields a plateau 40Ar–39Ar age of 131.3 ± 1.3 Ma. These results confirm a genetic link between the volcanism and associated Cu–Au mineralization. The Tongjing Cu–Au deposit in the Ningwu basin is genetically and possibly tectonically similar to alkaline intrusion-related gold deposits elsewhere in the world.  相似文献   

18.
The Dalucao deposit, located in western Sichuan Province, southwestern China, in the western part of the Yangtze Craton, is one of the largest and most extensive rare earth element (REE) deposits in the Himalayan Mianning–Dechang REE belt. Moreover, the Dalucao deposit is the only deposit identified in the southern part of the belt. The Dalucao deposit contains the No. 1, 2, and 3 orebodies; the No. 1 and 3 orebodies are both hosted in two breccia pipes, located in syenite–carbonatite host rocks. Both pipes have elliptical cross-sections at the surface, with long-axis diameters of 200–400 m and short-axis diameters of 180–200 m; the pipes extend downwards for > 450 m. No. 1 and No. 3 have total thickness varying between 55 and 175 m and 14 to 58 m respectively. The REE mineralization is associated with four brecciation events, which are recorded in each of the pipes. The ore grades in the No. 1 and 3 orebodies are similar, and consist of 1.0%–4.5% rare earth oxides (REOs). The No. 1 orebody is characterized by a Type I mineral assemblage (fluorite + barite + celestite + bastnäsite), whereas the No. 3 orebody is characterized by a Type II assemblage (fluorite + celestite + pyrite + muscovite + bastnäsite + strontianite). Argon (40Ar/39Ar) dating of hydrothermal muscovite intergrown with REE minerals in typical ores from the No. 1 and 3 orebodies yielded similar ages of 12.69 ± 0.13 and 12.23 ± 0.21 Ma, respectively, which suggest that both mineral assemblages formed coevally, rather than in paragenetic stages. Both ages are also similar to the timing of intrusion of the syenite–carbonatite complex (12.13 ± 0.19 Ma). The ore-mineral assemblages occur in breccias, veinlets, and in narrow veins. The ore veinlets, which usually show a transition to mineralized breccia or brecciated ores, are commonly enveloped by narrow veins and stringer zones with comparable mineral assemblages. The brecciated ores form 95% of the volume of the deposit, whereas brecciated ores are only a minor constituent of other deposits in the Mianning–Dechang REE belt. The carbonatite in the syenite–carbonatite complexes contains high concentrations of S (0.07–2.32 wt.%), Sr (16,500–20,700 ppm), Ba (3600–8400 ppm), and light REEs (LREE) (2848–10,768 ppm), but is depleted in high-field-strength elements (HFSE) (Nb, Ta, P, Zr, Hf, and Ti). The syenite is moderately enriched in large-ion lithophile elements (LILE), Sr (155–277 ppm), and Ba (440–755 ppm). The mineralized, altered, and fresh syenites and carbonatites exhibit similar trace element compositions and REE patterns. Brecciation events, and the Dalucao Fault and its secondary faults around the deposit, contributed to the REE mineralization by facilitating the circulation of ore-forming fluids and providing space for REE precipitation. Some hydrothermal veins composed of coarse-grained fluorite and quartz are distributed in the syenite–carbonatite complex. The oxygen isotope compositions of ore-forming fluids in equilibrium with quartz at 215 °C are − 4.95‰ to − 7.45‰, and the hydrogen isotope compositions of fluid inclusions in coarse-grained quartz are − 88.4‰ to − 105.1‰. The syenite–carbonatite complex and carbonatite are main contributors to the mineralization in the geological occurrence. Thus, the main components of the ore-forming fluids were magmatic water, meteoric water, and CO2 derived from the decarbonation of carbonatite. According to the petrographic studies, bastnäsite mineralization developed during later stages of hydrothermal evolution and overprinted the formation of the brecciated fluorite–quartz hydrothermal veins. As low-temperature isotope exchange between carbonates of the carbonatite and water-rich magmatic fluids will lead to positive shifts in δ18O values of the carbonates, C–O isotopic compositions from the bulk primary carbonatite to hydrothermal calcite and bastnäsite changed (δ18OV-SMOW from 8.0‰ to 11.6‰, and δ13C V-PDB from − 6.1 to − 8.7‰). According to the chemical composition of syenite and carbonatite, REE chloride species are the primary complexes for the transport of the REEs in the hydrothermal fluids, and the presence of bastnäsite and parisite means the REE were precipitated as fluorocarbonates. High contents of Sr, Ba and S in the syenite–carbonatite complex led to the deposition of large amount of barite and celestite.  相似文献   

19.
The Xiongcun district, located in the western segment of the Gangdese porphyry copper belt (GPCB), hosts the only known Jurassic mineralization in the GPCB, Tibet, PRC. The No. I deposit in the Xiongcun district is related to the Middle Jurassic quartz diorite porphyry (167–161 Ma) and the mineralization was formed at ca. 161.5 ± 2.7 Ma. Ore-bearing Middle Jurassic quartz diorite porphyry emplaced into the Early Jurassic volcano-sedimentary rock sequences of the Xiongcun Formation. Veinlets and disseminated mineralization developed within the Middle Jurassic quartz diorite porphyry and the surrounding metamorphosed tuff, hosting a measured and indicated resource of 1.04 Mt copper, 143.31 t gold and 900.43 t silver with an average grade of 0.48% copper, 0.66 g/t gold, and 4.19 g/t silver. The mineralization can be assigned to four stages, including three main stages of hypogene mineralization and one epigenetic stage. The main alteration associated with mineralization is potassic. Seven mineralization-related hydrothermal veins have been recognized, including quartz–sulfide, biotite–sulfide, magnetite–sulfide, quartz–molybdenite–sulfide, chalcopyrite–pyrite–pyrrhotite, pyrite and polymetallic veins. The S and Pb isotopic compositions of the ore sulfides and the Re contents of the molybdenite suggest a mantle source for the ore-forming materials with minor contamination from the subducted sediments. Hydrogen and oxygen isotope compositions of quartz in the ores suggest that both magmatic and meteoric waters were involved in the ore-forming process. The ore-bearing porphyry (167–161 Ma) and ore-forming (161.5 ± 2.7 Ma) ages of the No. I deposit correspond to the time of northward subduction of Neo-Tethys oceanic slab. The geochemical data of the ore-bearing porphyry indicate that the No. I deposit formed in an intra-oceanic island arc setting and the ore-bearing porphyry originated from the partial melting of mantle with limited contribution of subducted sediments. The genesis of the ore-bearing porphyry and No. I deposit is interpreted as being related to northward intra-oceanic subduction of Neo-Tethys oceanic slab in the Middle Jurassic time (167–161 Ma).  相似文献   

20.
The Lanping basin is a significant Pb–Zn–Cu–Ag mineralization belt of the Sanjiang Tethyan metallogenic province in China. Over 100 thrust-controlled, sediment-hosted, Himalayan base metal deposits have been discovered in this basin, including the largest sandstone-hosted Pb–Zn deposit in the world (Jinding), and several Cu ± Ag ± Co deposits (Baiyangping, Baiyangchang and Jinman). These deposits, with total reserves of over 16.0 Mt Pb + Zn, 0.6 Mt Cu, and 7000 t Ag, are mainly hosted in Meso-Cenozoic mottled clastic rocks, and strictly controlled by two Cenozoic thrust systems developed in the western and eastern segments of the Lanping basin.To define the metallogenic history of the study area, we dated nine calcite samples associated with copper sulfides from the Jinman Cu deposit by the Sm–Nd method and five molybdenite samples from the Liancheng Cu–Mo deposit by the Re–Os method. The calcite Sm–Nd age for the Jinman deposit (58 ± 5 Ma) and the molybdenite Re–Os age for the Liancheng deposit (48 ± 2 Ma), together with previously published chronological data, demonstrate (1) the Cu–Ag mineralization in the western Lanping basin mainly occurred in three episodes (i.e., ∼56–54, 51–48, and 31–29 Ma), corresponding to the main- and late-collisional stages of the Indo–Asian orogeny; and (2) the Pb–Zn–Ag (±Cu) mineralization in the eastern Lanping basin lacked precise and direct dating, however, the apatite fission track ages of several representative deposits (21 ± 4 Ma to 32 ± 5 Ma) may offer some constraints on the mineralization age.  相似文献   

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