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1.
Complex (δ18O, δ13C, 87Sr/86Sr, 143Nd/144Nd, and REE composition) data were obtained on quartz-carbonate veins in metasedimentary rocks to elucidate the material sources and to evaluate fluid regime during low-sulfide gold-quartz ore mineralization at the Sukhoi Log deposit. In order to use an oxygen isotopic thermometry for quartz veins, we calibrated empirical dependence of fractionation factors between vein quartz and altered wall rocks. The temperature range of quartz equilibration with wall rocks was evaluated at 380–190°C. Independent temperatures obtained using this thermometer indicate that the vein ankerite can be both earlier and later than vein quartz. The isotopic systematics (δ13C and δ18O) of ankerite in the quartz-carbonate veins, carbonates in the ore-hosting shales of the Khomolkho and Imnyakh formations both within and outside mineralized zones at the deposit indicate that the ore-hosting rocks and veins in the mineralized zone contain incoming carbonate, which was most probably borrowed from the carbonate rocks of the Imnyakh Formation. REE composition of vein ankerite shows that these elements were transported by fluid as carbonate complexes. The behavior of the Eu/Eu* and (La/Yb)n ratios and Mn of the vein ankerite suggest that during carbonate crystallization the system was closed with respect to fluid. Sr-Nd isotope systematics indicates that the isotopic parameters of the vein ankerite were formed with the participation of metasedimentary host rocks of both the Imnyakh and Khomolkho formations, which are contrastingly different in Nd isotopic composition. A fluid/rock ratio during metasomatic processes in the wall rocks was calculated for two scenarios of their thermal history: with a continuously operating heat source beneath the Sukhoi Log structure and with a linear cooling of the structure. The effective integral W/R ratios calculated lie within the range of 0.046–0.226 and suggest that the veins were produced with the metamorphic fluid. Low W/R ratios are inconsistent with the mechanism of vein quartz crystallization due to fluid oversaturation with respect to SiO2 at decreasing temperature. We believe that the main mechanism responsible for the origin of these veins was variations of fluid oversaturation due to pressure variations (pressure solution mechanism). This hypothesis is consistent with the reported isotopic-geochemical characteristics of the wall rocks at the Sukhoi Log deposit.  相似文献   

2.
Oxygen isotopic composition was studied in the altered host rocks of the Dal’negorsk borosilicate deposit in order to establish a boron source and the origin of ore-forming fluids responsible for deposition of economic borosilicate ore. The relationships between oxygen isotopic composition and geochemistry of the altered igneous rocks occupying various structural and temporal positions in the ore zone were studied, including premineral high-potassium minor intrusions located in the zones of datolite mineralization; alkali basalt, gabbro, and breccia from the sedimentary framework of the deposit; and postmineral basaltic andesite, basalt, and dolerite dikes. It was suggested that interaction of aqueous fluid with host rocks brought about not only variation in oxygen isotopic composition but also shifts in geochemistry of these rocks, especially as concerns the chemical elements contained in ore-forming fluid. The disturbance of oxygen isotopic system is typical of all studied rocks: δ18O values sharply decrease indicating interaction with aqueous fluid at elevated temperatures. The lowest δ18O (from −2.9 to +0.1‰) is characteristic of the premineral high-potassium and ultrapotassium minor intrusions from skarn-datolite zone. Igneous rocks from the sedimentary framework of the deposit have δ18O of +2 to −0.9‰ The δ18O of postmineral basaltic andesite, basalt, and dolerite dikes varies from 0 to +7‰ with increasing distance from the ore zone. The oxygen isotopic composition of aqueous fluid evidences its exogenic origin. The geochemical and isotopic characteristics of ore-forming fluid show that it could have been deep-seated subsurface water similar to the contemporary water of the Alpine fold zone, which contain up to 700–1000 mg/l B and is distinguished by high K, Li, Rb, Cs contents and high K/Na ratio. Similar geochemistry is characteristic of the fluid inclusions in quartz from ore zones. It cannot be ruled out that continental evaporites were a source of boron as well. The relationships between δ18O, K-Ar age, and geochemical parameters of premineral and postmineral altered intrusive bodies allow us to suggest that the subsurface B-bearing water discharged through narrow channels controlled by premineral basaltic bodies. The discharge was probably initiated by emplacement of basalt and dolerite dikes.  相似文献   

3.
The Géant Dormant gold mine is a sulfide-rich quartz vein gold deposit hosted by a volcano-sedimentary sequence and an associated felsic endogenous dome and dikes. The auriferous quartz-sulfide veins were preceded by two synvolcanic gold-bearing mineralizing events: early sulfidic seafloor-related and later disseminated pyrite in the felsic dome. This deposit differs from classical Archean auriferous quartz vein deposits by the low carbonate and high sulfide contents of the veins and by their formation prior to ductile penetrative deformation. The δ18O values of quartz associated with seafloor-related auriferous sulfides average 11.9 ± 0.6‰ (n = 3). The seafloor hydrothermal fluids had a δ18O value of 3.2‰ calculated at 250 °C. The oxygen isotope composition of quartz and chlorite from veins average 12.5 ± 0.3‰ (n = 20) and 5.9 ± 1.1‰ (n = 4) respectively. Assuming oxygen isotope equilibrium between quartz and chlorite, the veins formed at a temperature of ∼275 °C, which is consistent with the calculated temperature of 269 ± 10 °C from chlorite chemistry. The gold-bearing fluids had a δ18O value of 4.7‰ calculated at 275 °C. The δ34S values of sulfides from the three gold events range from 0.6 to 2.8‰ (n = 32) and are close to magmatic values. Sulfur isotope geothermometry constrains the sulfide precipitation in the gold-bearing veins at a temperature of ∼350 °C. The similarity of the isotope data, the calculated δ18O of the mineralizing fluids and the likely seawater fluid source suggest that the three mineralizing events are genetically related to a volcanogenic hydrothermal system. The high value of the auriferous fluids (δ18O = 4.7‰) is attributed to a significant magmatic fluid contribution to the evolved seawater-dominated convective hydrothermal system. The two-stage filling of veins at increasing temperature from quartz-chlorite (275 °C) to sulfides (350 °C) may reflect the progressive maturation of volcanogenic hydrothermal systems. These results, together with field and geochemical data, suggest that formation of gold-rich volcanogenic systems require specific conditions that comprise a magmatic fluid contribution and gold from arc-related felsic rocks, coeval with the mineralizing events. This study shows that some auriferous quartz-vein orebodies in Archean terranes are formed in volcanogenic rather than mesothermal systems. Received: 12 December 1998 / Accepted: 5 July 1999  相似文献   

4.
A set of sheeted quartz veins cutting 380 Ma monzogranite at Sandwich Point, Nova Scotia, Canada, provide an opportunity to address issues regarding fluid reservoirs and genesis of intrusion-related gold deposits. The quartz veins, locally with arsenopyrite (≤5%) and elevated Au–(Bi–Sb–Cu–Zn), occur within the reduced South Mountain Batholith, which also has other zones of anomalous gold enrichment. The host granite intruded (P = 3.5 kbars) Lower Paleozoic metaturbiditic rocks of the Meguma Supergroup, well known for orogenic vein gold mineralization. Relevant field observations include the following: (1) the granite contains pegmatite segregations and is cut by aplitic dykes and zones (≤1–2 m) of spaced fracture cleavage; (2) sheeted veins containing coarse, comb-textured quartz extend into a pegmatite zone; (3) arsenopyrite-bearing greisens dominated by F-rich muscovite occur adjacent the quartz veins; and (4) vein and greisen formation is consistent with Riedel shear geometry. Although these features suggest a magmatic origin for the vein-forming fluids, geochemical studies indicate a more complex origin. Vein quartz contains two types of aqueous fluid inclusion assemblages (FIA). Type 1 is a low-salinity (≤3 wt.% equivalent NaCl) with minor CO2 (≤2 mol%) and has T h = 280–340°C. In contrast, type 2 is a high-salinity (20–25 wt.% equivalent NaCl), Ca-rich fluid with T h = 160–200°C. Pressure-corrected fluid inclusion data reflect expulsion of a magmatic fluid near the granite solidus (650°C) that cooled and mixed with a lower temperature (400°C), wall rock equilibrated, Ca-rich fluid. Evidence for fluid unmixing, an important process in some intrusion-related gold deposit settings, is lacking. Stable isotopic (O, D, S) analyses for quartz, muscovite and arsenopyrite samples from vein and greisens indicate the following: (1) δ18Oqtz = +11.7‰ to 17.8‰ and δ18Omusc = +10.7‰ to +11.2‰; (2) δDmusc = −44‰ to−54‰; and (3) δ34Saspy = +7.8‰ to +10.3‰. These data are interpreted, in conjunction with fluid inclusion data, to reflect contamination of a magmatic-derived fluid (d18OH2O {\delta^{{{18}}}}{{\hbox{O}}_{{{{\rm{H}}_{{2}}}{\rm{O}}}}}  ≤ +10‰) by an external fluid (d18OH2O {\delta^{{{18}}}}{{\hbox{O}}_{{{{\rm{H}}_{{2}}}{\rm{O}}}}}  ≥ +15‰), the latter having equilibrated with the surrounding metasedimentary rocks. The δ34S data are inconsistent with a direct igneous source based on other studies for the host intrusion (d18OH2O {\delta^{{{18}}}}{{\hbox{O}}_{{{{\rm{H}}_{{2}}}{\rm{O}}}}}  = +5‰) and are, instead, consistent with an external reservoir for sulphur based on δ34SH2S data for the surrounding metasedimentary rocks. Divergent fluid reservoirs are also supported by analyses of Pb isotopes for pegmatitic K-feldspar and vein arsenopyrite. Collectively the data indicate that the vein- and greisen-forming fluids had a complex origin and reflect both magmatic and non-magmatic reservoirs. Thus, although the geological setting suggests a magmatic origin, the geochemical data indicate involvement of multiple reservoirs. These results suggest multiple reservoirs for this intrusion-related gold deposit setting and caution against interpreting the genesis of intrusion-related gold deposit mineralization in somewhat analogous settings based on a limited geochemical data set.  相似文献   

5.
The Jinshan orogenic gold deposit is a world-class deposit hosted by a ductile shear zone caused by a transpressional terrane collision during Neoproterozoic time. Ore bodies at the deposit include laminated quartz veins and disseminated pyrite-bearing mylonite. Most quartz veins in the shear zone, with and without gold mineralization, were boudinaged during progressive shear deformation with three generations of boudinage structures produced at different stages of progressive deformation. Observations of ore-controlling structures at various scales indicate syn-deformational mineralization. Fluid inclusions from pyrite intergrown with auriferous quartz have 3He/4He ratios of 0.15–0.24 Ra and 40Ar/36Ar ratios 575–3,060. δ18Ofluid values calculated from quartz are 5.5–8.4‰, and δD values of fluid inclusions contained in quartz range between −61‰ and −75‰. The δ13C values of ankerite range from −5.0‰ to −4.2‰, and ankerite δ18O values from 4.4‰ to 8.0‰. The noble gas and stable isotope data suggest a predominant crustal source of ore fluids with less than 5% mantle component. Data also show that in situ fluids were generated locally by pervasive pressure solution, and that widespread dissolution seams acted as pathways of fluid flow, migration, and precipitation. The in situ fluids and fluids derived from deeper levels of the crust were focused by deformation and deformation structures at various scales through solution-dissolution creep, crack-seal slip, and cyclic fault-valve mechanisms during progressively localized deformation and gold mineralization.  相似文献   

6.
New mineralogical, thermobarometric, isotopic, and geochemical data provide evidence for long and complex formation history of the Sarylakh and Sentachan Au-Sb deposits conditioned by regional geodynamics and various types of ore mineralization, differing in age and source of ore matter combined in the same ore-localizing structural units. The deposits are situated in the Taryn metallogenic zone of the East Yakutian metallogenic belt in the central Verkhoyansk-Kolyma Fold Region. They are controlled by the regional Adycha-Taryn Fault Zone that separates the Kular-Nera Terrane and the western part of the Verkhoyansk Fold-Thrust Belt. The fault extends along the strike of the northwest-trending linear folds and is deep-rooted and repeatedly reactivated. The orebodies are mineralized crush zones accompanied by sulfidated (up to 100 m wide) quartz-sericite metasomatic rocks and replacing dickite-pyrophyllite alteration near stibnite veinlets. Two stages of low-sulfide gold-quartz and stibnite mineralization are distinguished. The formation conditions of the early milk white quartz in orebodies with stibnite mineralization at the Sarylakh and Sentachan deposits are similar: temperature interval 340–280°C, salt concentration in fluids 6.8–1.6 wt % NaCl equiv, fluid pressure 3430–1050 bar, and sodic bicarbonate fluid composition. The ranges of fluid salinity overlapped at both deposits. In the late regenerated quartz that attends stibnite mineralization, fluid inclusions contain an aqueous solution with salinity of 3.2 wt % NaCl equiv and are homogenized into liquid at 304–189°C. Syngenetic gas inclusions contain nitrogen 0.19 g/cm3 in density. The pressure of 300 bar is estimated at 189°C. The composition of the captured fluid is characterized as K-Ca bicarbonatesulfate. The sulfur isotopic composition has been analyzed in pyrite and arsenopyrite from ore and metasomatic zones, as well as in coarse-, medium-, and fine-grained stibnite varieties subjected to dynamometamorphism. The following δ34S values, ‰ have been established at the Sarylakh deposit: −2.0 to −0.9 in arsenopyrite, −5.5 to −1.1 in pyrite, and −5.5 to −3.6 in stibnite. At the Sentachan deposit: −0.8 to +1.0 in arsenopyrite, +0.5 to +2.6 in pyrite, and −3.9 to +0.6 in stibnite. Sulfides from the Sentachan deposit is somewhat enriched in 34S. The 18O of milk white quartz at the Sarylakh deposit varies from +14.8 to 17.0‰ and from +16.4 to + 19.3‰ at the Sentachan. The δ18O of regenerated quartz is +16.5‰ at the Sarylakh and +17.6 to +19.8‰ at the Sentachan. The δ18O of carbonates varies from +15.0 to 16.3% at the Sarylakh and from +16.7 to +18.2‰ at the Sentachan. The δ13C of carbonates ranges from −9.5 to −12.1‰ and −7.8 to −8.5‰, respectively. The calculated $ \delta ^{18} O_{H_2 O} $ \delta ^{18} O_{H_2 O} of the early fluid in equilibrium with quartz and dolomite at 300δC are +7.9 to +10.1‰ for the Sarylakh deposit and +9.5 to +12.4‰ for the Sentachan deposit (+4.9 and 6.0‰ at 200°C for the late fluid, respectively). Most estimates fall into the interval characteristic of magmatic water (°18O = +5.5 to +9.5‰).  相似文献   

7.
The Jinwozi gold deposit consists of gold-bearing quartz veins in a biotite granodiorite of Hercynian age (zircon U-Pb age ≈ 335.7 Ma). Ore mineralogy is simple. In addition to native gold, there are only small amounts of sulfides, mainly pyrite and minor sphalerite, chalcopyrite and galena. δ34S values average 6.69‰, and δ18O 13.99‰ Abundant CO2 is contained in fluid inclusions from quartz. Homogenization temperatures of fluid inclusions are between 186 and 262 °C. REE distribution patterns indicate that the igneous mass may have been derived from a common initial material of calcareous-argillaceous sediments and alkali basalts as the country rocks. In other words, the Jinwozi granodiorite is of remelting origin from crustal material. Isotopic evidence of S, O and Pb shows that the ore-forming material is genetically related to magmatic hydrothermal activity.  相似文献   

8.
Fluid inclusions in granite quartz and three generations of veins indicate that three fluids have affected the Caledonian Galway Granite. These fluids were examined by petrography, microthermometry, chlorite thermometry, fluid chemistry and stable isotope studies. The earliest fluid was a H2O-CO2-NaCl fluid of moderate salinity (4–10 wt% NaCl eq.) that deposited late-magmatic molybdenite mineralised quartz veins (V1) and formed the earliest secondary inclusions in granite quartz. This fluid is more abundant in the west of the batholith, corresponding to a decrease in emplacement depth. Within veins, and to the east, this fluid was trapped homogeneously, but in granite quartz in the west it unmixed at 305–390 °C and 0.7–1.8 kbar. Homogeneous quartz δ18O across the batholith (9.5 ± 0.4‰n = 12) suggests V1 precipitation at high temperatures (perhaps 600 °C) and pressures (1–3 kbar) from magmatic fluids. Microthermometric data for V1 indicate lower temperatures, suggesting inclusion volumes re-equilibrated during cooling. The second fluid was a H2O-NaCl-KCl, low-moderate salinity (0–10 wt% NaCl eq.), moderate temperature (270–340 °C), high δD (−18 ± 2‰), low δ18O (0.5–2.0‰) fluid of meteoric origin. This fluid penetrated the batholith via quartz veins (V2) which infill faults active during post-consolidation uplift of the batholith. It forms the most common inclusion type in granite quartz throughout the batholith and is responsible for widespread retrograde alteration involving chloritization of biotite and hornblende, sericitization and saussuritization of plagioclase, and reddening of K-feldspar. The salinity was generated by fluid-rock interactions within the granite. Within granite quartz this fluid was trapped at 0.5–2.3 kbar, having become overpressured. This fluid probably infiltrated the Granite in a meteoric-convection system during cooling after intrusion, but a later age cannot be ruled out. The final fluid to enter the Granite and its host rocks was a H2O-NaCl-CaCl2-KCl fluid with variable salinity (8–28 wt% NaCl eq.), temperature (125–205 °C), δD (−17 to −45‰), δ18O (−3 to + 1.2‰), δ13CCO2 (−19 to 0‰) and δ34Ssulphate (13–23‰) that deposited veins containing quartz, fluorite, calcite, barite, galena, chalcopyrite sphalerite and pyrite (V3). Correlations of salinity, temperature, δD and δ18O are interpreted as the result of mixing of two fluid end-members, one a high-δD (−17 to −8‰), moderate-δ18O (1.2–2.5‰), high-δ13CCO2 (> −4‰), low-δ34Ssulphate (13‰), high-temperature (205–230 °C), moderate-salinity (8–12 wt% NaCl eq.) fluid, the other a low-δD (−61 to −45‰), low-δ18O (−5.4 to −3‰), low-δ13C (<−10‰), high-δ34Ssulphate (20–23‰) low-temperature (80–125 °C), high-salinity (21–28 wt% NaCl eq.) fluid. Geochronological evidence suggests V3 veins are late Triassic; the high-δD end-member is interpreted as a contemporaneous surface fluid, probably mixed meteoric water and evaporated seawater and/or dissolved evaporites, whereas the low-δD end-member is interpreted as a basinal brine derived from the adjacent Carboniferous sequence. This study demonstrates that the Galway Granite was a locus for repeated fluid events for a variety of reasons; from expulsion of magmatic fluids during the final stages of crystallisation, through a meteoric convection system, probably driven by waning magmatic heat, to much later mineralisation, concentrated in its vicinity due to thermal, tectonic and compositional properties of granite batholiths which encourage mineralisation long after magmatic heat has abated. Received: 3 April 1996 / Accepted: 5 May 1997  相似文献   

9.
The Mont-de-l’Aigle deposit is located in the northern part of Dome Lemieux, in the Connecticut Valley-Gaspé Synclinorium, Gaspé Peninsula, Québec. The Dome Lemieux is a subcircular antiform of Siluro–Devonian sedimentary rocks that is cut by numerous mafic and felsic sills and dikes of Silurian to Late Devonian age. Plutonism occurred in a continental within-plate extensional setting typical of orogenic collapse. The Cu−Fe (± Au) mineralization of Mont-de-l’Aigle occurs in veins, stockworks, and breccias. Mineralization is located near or within N−S and NW−SE faults cutting sedimentary rocks. IOCG mineralization postdates intrusions, skarns, hornfels, and epithermal mineralization typical of the southern part of the Dome Lemieux. The paragenetic sequence comprises: (1) pervasive sodic, potassic, chlorite, and silica alteration, (2) hematite, quartz, pyrite, magnetite, and chalcopyrite veins, stockworks and breccias and, (3) dolomite ± hematite veins and veinlets cutting the earlier mineralization. Intrusions display proximal sodic and potassic alteration, whereas sedimentary rocks have proximal decalcification, silicification, and potassic alteration. Both intrusive and sedimentary rocks are affected by a pervasive distal chlorite (± silica) alteration. The sulfur isotope composition of pyrite and chalcopyrite (δ34S=−1.5 to 4.8‰) suggests that sulfur was derived mainly from igneous rocks. Fluid δ18O (−0.4 to 2.65‰) indicates meteoric or seawater that reacted with the country rocks. Mixing of hot magmatic fluids with a cooler fluid, perhaps meteoric or seawater is suggested for mineral deposition and alteration of the Mont-de-l’Aigle deposit. The mineralogy, alteration, and sulfur isotope composition of the Mont-de-l’Aigle deposit compare well with IOCG deposits worldwide, making the Mont-de-l’Aigle deposit a rare example of Paleozoic IOCG mineralization, formed at shallow depth, within a low metamorphic grade sedimentary rock sequence.  相似文献   

10.
In order to reconstruct the formation and exhumation mechanisms of UHP metamorphic terrains, the Chinese Continental Scientific Drilling Program (CCSD) has been carried out in Donghai of the Dabie-Sulu ultrahigh-pressure (UHP) metamorphic belt, East China. Eclogite, gneiss, amphibolite (retrograded from eclogite), ultramafic rocks, and minor schist and quartzite have been drilled. Aiming to reveal the fluid behaviour in a vertical sequence of an UHP slab, we investigated fluid inclusion and oxygen isotope characteristics of selected drillcores from the main hole and the pilot-holes PP2 and ZK 703 of the CCSD. More than 540 laser-ablation oxygen isotope analyses on garnet, omphacite, quartz, kyanite, amphibole, phengite, rutile, epidote, amphibole, plagioclase, and biotite from various rocks in the depth range of 0–3,000 m (mainly eclogite and gneiss) show that the investigated rocks can be divided into two groups: 18O-depleted rocks (as low as δ18O = −7.4‰ for garnet) indicate interaction with cold climate meteoric waters, whereas 18O-normal rocks (with bulk δ18O > +5.6‰) have preserved the O-isotopic compositions of their protoliths. Meteoric water/rock interaction has reached depths of at least 2,700 m. Oxygen isotope equilibrium has generally been achieved. Isotopic compositions of mineral phases are homogeneous on a mm to cm scale regardless of lithology, but heterogeneous on the scale of a few metres. Oxygen isotope distributions in the vertical sections favour an “in situ” origin of the UHP metamorphic rocks. The very negative δ18O eclogites usually have higher hydroxyl-mineral contents than the normal δ18O rocks, indicating higher water content during UHP metamorphism. Fluid inclusion data suggest that rocks with depleted 18O compositions have had different fluid histories compared to those with normal δ18O values. Rocks with depleted 18O mainly have primary medium-to-high salinity inclusions in omphacite, kyanite and quartz, and abundant secondary low-salinity or pure water inclusions in quartz, indicating a high-salinity-brine-dominated fluid system during peak UHP metamorphism; no carbonic inclusions have been identified in these rocks. By contrast, primary very high-density CO2 inclusions are commonly found in the rocks with normal δ18O values. These observations suggest that fluid and oxygen isotope composition of minerals are related and reflect variable degrees of alterations of the Dabie-Sulu UHP metamorphic rocks.  相似文献   

11.
The chemistry, REE patterns, and carbon and oxygen isotopic compositions of carbonates from ore veins of the Darasun deposit are discussed. In addition to the earlier described siderite, calcite, and carbonates of the dolomite-ankerite series, kutnahorite is identified. The total REE content in Fe-Mg carbonates of the dolomite-ankerite series (2.8–73 ppm) is much lower than in later calcite (18–390 ppm). δ13C of Fe-Mg carbonates and calcite varies from +1.1 to −6.7‰ and from −0.9 to −4.9‰, respectively. δ18O of Fe-Mg carbonates and calcite varies from +17.6 to 3.6‰ and from +15.7 to −0.5‰, respectively. The REE sum and carbon and oxygen isotopic compositions reveal zonal distribution relative to the central granodiorite porphyry stock. The correlation between the carbon and oxygen isotopic compositions and REE sum reflects variations in the physicochemical formation conditions and composition of ore-forming fluid. The isotopic composition of fluid is calculated, and possible sources of its components are considered. Earlier established evidence for a magmatic source of ore-forming fluid and participation of meteoric water in ore formation is confirmed. Geochemical evidence for interaction of ore-forming fluid with host rocks is furnished. The relationships between the REE sum, on the one hand, and carbon and oxygen isotopic compositions of hydrothermal ore-forming fluid, on the other, are established.  相似文献   

12.
The Camagüey district, Cuba, is known for its epithermal precious metal deposits in a Cretaceous volcanic arc setting. Recently, the La Unión prospect was discovered in the southern part of the district, containing gold and minor copper mineralization interpreted as porphyry type. Mineralization is hosted in a 73.0 ± 1.5 Ma calc–alkaline I-type oxidized porphyry quartz diorite intrusive within volcanic and volcaniclastic rocks of the early Cretaceous Guáimaro Formation. The porphyry is affected by propylitic alteration and crosscut by a network of quartz and carbonate veinlets and veins. Chlorite, epidote, sericite, quartz, and pyrite are the main minerals in the early veins which are cut by late carbonate and zeolite veins. Late barite pseudomorphously replaces pyrite. Gold is associated with pyrite as disseminations in the altered quartz diorite and in the veins, occurring as inclusions or filling fractures in pyrite with 4 g/t Au in bulk samples, and up to 900 ppm Au in in pyrite. Fluid inclusion and oxygen isotope data are consistent with a H2O–NaCl–(KCl) mineralizing fluid, derived from the quartz diorite magma, and trapped at least at 425°C and 1.2 kbar. This primary fluid unmixed into two fluid phases, a hypersaline aqueous fluid and a low-salinity vapor-rich fluid. Boiling during cooling may have played an important role in metal precipitation. Pyrite δ34S values for the La Unión prospect range between 0.71‰ and 1.31‰, consistent with a homogeneous magmatic sulfur source. The fluids in equilibrium with the mineralized rocks have estimated δ18O values from 8‰ to 11.8‰, calculated for a temperature range of 480–505°C. The tectonic environment of the La Unión prospect, its high gold and low copper contents, the physical–chemical characteristics of the mineralizing fluids and the isotopic signature of the alteration minerals and fluids indicate that the La Unión gold mineralization is similar to the porphyry gold type, even though the ore-related epidote–chlorite alteration can be classified as propylitic and not the classic potassic and/or phyllic alteration. The low copper contents in the prospect could be due to a mineralizing fluid previously saturated in copper, which is indicated by trapped chalcopyrite crystals in high-temperature fluid inclusions. The low-temperature paragenesis, represented by carbonate, zeolite and barite, indicates epithermal overprint. The study shows the potential for other gold porphyry-type deposits in the Cretaceous volcanoplutonic arc of Cuba.  相似文献   

13.
 Late Proterozoic to Cambrian carbonate rocks from Lone Mountain, west central Nevada, record multiple post-depositional events including: (1) diagenesis, (2) Mesozoic regional metamorphism, (3) Late Cretaceous contact metamorphism, related to the emplacement of the Lone Mountain granitic pluton and (4) Tertiary hydrothermal alteration associated with extension, uplift and intrusion of silicic porphyry and lamprophyre dikes. Essentially pure calcite and dolomite marbles have stable isotopic compositions that can be divided into two groups, one with positive δ13C values from+3.1 to +1.4 ‰ (PDB) and high δ18O values from +21.5 to +15.8 ‰ (SMOW), and the other with negative δ13C values from –3.3 to –3.6‰ and low δ18O values from +16.9 to +11.1‰. Marbles also contain minor amounts of quartz, muscovite and phlogopite. Brown and blue luminescent, clear, smooth textured quartz grains from orange luminescent calcite marbles have high δ18O values from +23.9 to +18.1‰, while brown luminescent, opaque, rough textured quartz grains from red luminescent dolomite marbles typically have low δ18O values from +2.0 to +9.3‰. The δ18O values of muscovite and phlogopite from marbles are typical of micas in metamorphic rocks, with values between +10.4 and +14.4‰, whereas mica δD values are very depleted, varying from −102 to −156‰. No significant lowering of the δ18O values of Lone Mountain carbonates is inferred to have occurred during metamorphism as a result of devolatilization reactions because of the essentially pure nature of the marbles. Bright luminescence along the edges of fractures, quartz cements and quartz overgrowths in dolomite marbles, low δD values of micas, negative δ13C values and low δ18O values of calcite and dolomite, and depleted δ18O values of quartz from dolomite marbles all indicate that meteoric fluids interacted with Lone Mountain marbles during the Tertiary. Partial oxygen isotopic exchange between calcite and low 18O meteoric fluids lowered the δ18O values of calcite, resulting in uniform quartz-calcite fractionations that define an apparent pseudoisotherm. These quartz-calcite fractionations significantly underestimate both the temperature of metamorphism and the temperature of post-metamorphic alteration. Partial oxygen isotopic exchange between quartz and meteoric fluids also resulted in 18O depletion of quartz from dolomite marbles. This partial exchange was facilitated by an increase in the surface area of the quartz as a result of its dissolution by meteoric fluids. The negative δ13C values in carbonates result from the oxidation of organic material by meteoric fluids following metamorphism. Stable isotopic data from Lone Mountain marbles are consistent with the extensive circulation of meteoric hydrothermal fluids throughout western Nevada in Tertiary time. Received: 1 February 1994/Accepted: 12 September 1995  相似文献   

14.
At Sams Creek, a gold-bearing, peralkaline granite porphyry dyke, which has a 7 km strike length and is up to 60 m in thickness, intrudes camptonite lamprophyre dykes and lower greenschist facies metapelites and quartzites of the Late Ordovician Wangapeka formation. The lamprophyre dykes occur as thin (< 3 m) slivers along the contacts of the granite dyke. δ18Omagma values (+5 to +8‰, VSMOW) of the A-type granite suggest derivation from a primitive source, with an insignificant mature crustal contribution. Hydrothermal gold–sulphide mineralisation is confined to the granite and adjacent lamprophyre; metapelite country rocks have only weak hydrothermal alteration. Three stages of hydrothermal alteration have been identified in the granite: Stage I alteration (high fO2) consisting of magnetite–siderite±biotite; Stage II consisting of thin quartz–pyrite veinlets; and Stage III (low fO2) consisting of sulphides, quartz and siderite veins, and pervasive silicification. The lamprophyre is altered to an ankerite–chlorite–sericite assemblage. Stage III sulphide veins are composed of arsenopyrite + pyrite ± galena ± sphalerite ± gold ± chalcopyrite ± pyrrhotite ± rutile ± graphite. Three phases of deformation have affected the area, and the mineralised veins and the granite and lamprophyre dykes have been deformed by two phases of folding, the youngest of which is Early Cretaceous. Locally preserved early-formed fluid inclusions are either carbonic, showing two- or three-phases at room temperature (liquid CO2-CH4 + liquid H2O ± CO2 vapour) or two-phase liquid-rich aqueous inclusions, some of which contain clathrates. Salinities of the aqueous inclusions are in the range of 1.4 to 7.6 wt% NaCl equiv. Final homogenisation temperatures (Th) of the carbonic inclusions indicate minimum trapping temperatures of 320 to 355°C, which are not too different from vein formation temperatures of 340–380°C estimated from quartz–albite stable isotope thermometry. δ18O values of Stage II and III vein quartz range from +12 and +17‰ and have a bimodal distribution (+14.5 and +16‰) with Stage II vein quartz accounting for the lower values. Siderite in Stage III veins have δ18O (+12 to +16‰) and δ13C values (−5‰, relative to VPDB), unlike those from Wangapeka Formation metasediments (δ13Cbulk carbon values of −24 to −19‰) and underlying Arthur Marble marine carbonates (δ18O = +25‰ and δ13C = 0‰). Calculated δ18Owater (+8 to +11‰, at 340°C) and (−5‰) values from vein quartz and siderite are consistent with a magmatic hydrothermal source, but a metamorphic hydrothermal origin cannot be excluded. δ34S values of sulphides range from +5 to +10‰ (relative to CDT) and also have a bimodal distribution (modes at +6 and +9‰, correlated with Stage II and Stage III mineralisation, respectively). The δ34S values of pyrite from the Arthur Marble marine carbonates (range from +3 to +13‰) and Wangapeka Formation (range from −4 to +9.5‰) indicate that they are potential sources of sulphur for sulphides in the Sams Creek veins. Another possible source of the sulphur is the lithospheric mantle which has positive values up to +14‰. Ages of the granite, lamprophyre, alteration/mineralisation, and deformation in the region are not well constrained, which makes it difficult to identify sources of mineralisation with respect to timing. Our mineralogical and stable isotope data does not exclude a metamorphic source, but we consider that the source of the mineralisation can best be explained by a magmatic hydrothermal source. Assuming that the hydrothermal fluids were sourced from crystallisation of the Sams Creek granite or an underlying magma chamber, then the Sams Creek gold deposit appears to be a hybrid between those described as reduced granite Au–Bi deposits and alkaline intrusive-hosted Au–Mo–Cu deposits.  相似文献   

15.
Whole rock oxygen isotope data are presented for the Panorama district, in the Archean Pilbara Craton of Western Australia, where near-perfect exposure reveals a cross section through a complete volcanogenic massive sulfide (VMS) hydrothermal alteration system. The δ18O values decrease with depth in the volcanic pile, across semi-conformable alteration zones, to values below 6‰ immediately above a large (180 km2) subvolcanic intrusion. Altered rocks in the upper parts of the subvolcanic intrusion have lower δ18O values (6–8‰) than least altered granite (8‰), apart from sericite–quartz altered zones, which are slightly higher (8–10‰). Corridors of low δ18O values crosscut this regional zonation, and are coincident with transgressive feldspar-destructive alteration zones, which underlie VMS mineralization. The whole rock oxygen isotope distribution patterns are interpreted to represent alteration temperature, where high δ18O values correspond to low temperature alteration and low δ18O values correspond to high temperature alteration. Alteration temperatures, which were calculated using modal alteration mineral abundances and an assumed fluid δ18O, are consistent with this interpretation. Increasing temperatures with depth in the volcanic pile and high temperatures in transgressive corridors leading up to VMS deposits, are consistent with a convective hydrothermal model, in which heat from the subvolcanic intrusion drove seawater through the volcanic pile. Granite-hosted sericite–quartz alteration zones are 18O-enriched, and are tentatively interpreted to have formed from a mixed magmatic-evolved seawater fluid. Received: 12 April 1999 / Accepted: 6 April 2000  相似文献   

16.
The Eastern Iberian Central System has abundant ore showings hosted by a wide variety of hydrothermal rocks; they include Sn-W, Fe and Zn-(W) calcic and magnesian skarns, shear zone- and episyenite-hosted Cu-Zn-Sn-W orebodies, Cu-W-Sn greisens and W-(Sn), base metal and fluorite-barite veins. Systematic dating and fluid inclusion studies show that they can be grouped into several hydrothermal episodes related with the waning Variscan orogeny. The first event was at about 295 Ma followed by younger pulses associated with Early Alpine rifting and extension and dated near 277, 150 and 100 to 20 Ma, respectively (events II–IV). The δ18O-δD and δ34S studies of hydrothermal rocks have elucidated the hydrological evolution of these systems. The event I fluids are of mixed origin. They are metamorphic fluids (H2O-CO2-CH4-NaCl; δ18O=4.7 to 9.3‰; δD ab.−34‰) related to W-(Sn) veins and modified meteoric waters in the deep magnesian Sn-W skarns (H2O-NaCl, 4.5–6.4 wt% NaCl eq.; δ18O=7.3–7.8‰; δD=−77 to −74‰) and epizonal shallow calcic Zn-(W) and Fe skarns (H2O-NaCl, <8 wt% NaCl eq.; δ18O=−0.4 to 3.4‰; δD=−75 to −58‰). They were probably formed by local hydrothermal cells that were spatially and temporally related to the youngest Variscan granites, the metals precipitating by fluid unmixing and fluid-rock reactions. The minor influence of magmatic fluids confirms that the intrusion of these granites was essentially water-undersaturated, as most of the hydrothermal fluids were external to the igneous rocks. The fluids involved in the younger hydrothermal systems (events II–III) are very similar. The waters involved in the formation of episyenites, chlorite-rich greisens, retrograde skarns and phyllic and chlorite-rich alterations in the shear zones show no major chemical or isotopic differences. Interaction of the hydrothermal fluids with the host rocks was the main mechanism of ore formation. The composition (H2O-NaCl fluids with original salinities below 6.2 wt% NaCl eq.) and the δ18O (−4.6 to 6.3‰) and δD (−51 to −40‰) values are consistent with a meteoric origin, with a δ18O-shift caused by the interaction with the, mostly igneous, host rocks. These fluids circulated within regional-scale convective cells and were then channelled along major crustal discontinuities. In these shear zones the more easily altered minerals such as feldspars, actinolite and chlorite had their δ18O signatures overprinted by low temperature younger events while the quartz inherited the original signature. In the shallower portions of the hydrothermal systems, basement-cover fluorite-barite-base metal veins formed by mixing of these deep fluids with downwards percolating brines. These brines are also interpreted as of meteoric origin (δ18O< ≈ −4‰; δD=−65 to −36‰) that leached the solutes (salinity >14 wt% NaCl eq.) from evaporites hosted in the post-Variscan sequence. The δD values are very similar to most of those recorded by Kelly and Rye in Panasqueira and confirm that the Upper Paleozoic meteoric waters in central Iberia had very negative δD values (≤−52‰) whereas those of Early Mesozoic age ranged between −65 and −36‰. Received: 9 June 1999 / Accepted: 19 January 2000  相似文献   

17.
The Longquanzhan gold deposit hosted in granitic cataclasites with mylontization of the foot wall of the main Yishui-Tangtou fault. 3He/4He ratios in fluid inclusions range from 0. 14 to 0. 24 R/Ra,close to those of the crust-source helium. 40Ar/36Ar ratios were measured to be 289-1811, slightly higher than those of atmospheric argon. The results of analysis of helium and argon isotopes suggested that ore-forming fluids were derived chiefly from the crust. The δ18O values of fluid inclusions from vein quartz range from -1.78‰ to 4.07‰, and the δD values of the fluid inclusions vary between -74‰ and -77‰. The hydrogen and oxygen isotope data indicated that the ore-forming fluid for the Longquanzhan gold deposit had mixed with meteoric water in the process of mineralization. This is consistent with the conclusion from the helium and argon isotope data.  相似文献   

18.
The Serrinha gold deposit of the Gurupi Belt, northern Brazil, belongs to the class of orogenic gold deposits. The deposit is hosted in highly strained graphitic schist belonging to a Paleoproterozoic (∼2,160 Ma) metavolcano-sedimentary sequence. The ore-zones are up to 11 m thick, parallel to the regional NW–SE schistosity, and characterized by quartz-carbonate-sulfide veinlets and minor disseminations. Textural and structural data indicate that mineralization was syn- to late-tectonic and postmetamorphic. Fluid inclusion studies identified early CO2 (CH4-N2) and CO2 (CH4-N2)-H2O-NaCl inclusions that show highly variable phase ratios, CO2 homogenization, and total homogenization temperatures both to liquid and vapor, interpreted as the product of fluid immiscibility under fluctuating pressure conditions, more or less associated with postentrapment modifications. The ore-bearing fluid typically has 18–33mol% of CO2, up to 4mol% of N2, and less than 2mol% of CH4 and displays moderate to high densities with salinity around 4.5wt% NaCl equiv. Mineralization occurred around 310 to 335°C and 1.3 to 3.0 kbar, based on fluid inclusion homogenization temperatures and oxygen isotope thermometry with estimated oxygen fugacity indicating relatively reduced conditions. Stable isotope data on quartz, carbonate, and fluid inclusions suggest that veins formed from fluids with δ18OH2O and δDH2O (310–335°C) values of +6.2 to +8.4‰ and −19 to −80‰, respectively, which might be metamorphic and/or magmatic and/or mantle-derived. The carbon isotope composition (δ13C) varies from −14.2 to −15.7‰ in carbonates; it is −17.6‰ in fluid inclusion CO2 and −23.6‰ in graphite from the host rock. The δ34S values of pyrite are −2.6 to −7.9‰. The strongly to moderately negative carbon isotope composition of the carbonates and inclusion fluid CO2 reflects variable contribution of organic carbon to an originally heavier fluid (magmatic, metamorphic, or mantle-derived) at the site of deposition and sulfur isotopes indicate some oxidation of the originally reduced fluid. The deposition of gold is interpreted to have occurred mainly in response to phase separation and fluid-rock interactions such as CO2 removal and desulfidation reactions that provoked variations in the fluid pH and redox conditions.  相似文献   

19.
Young orogenic gold mineralisation in active collisional mountains, Taiwan   总被引：1，自引：0，他引：1  
Gold-bearing vein systems in the high mountains of Taiwan are part of the youngest tectonic-hydrothermal system on Earth. Tectonic collision initiated in the Pliocene has stacked Eocene–Miocene marine sedimentary rocks to form steep mountains nearly 4 km high. Thinner portions of the sedimentary pile (∼5 km) are currently producing hydrocarbons in a fold and thrust belt, and orogenic gold occurs in quartz veins in thicker parts of the pile (∼10 km) in the Slate Belt that underlies the mountains. Metamorphic fluids (2–5 wt.% NaCl equivalent) are rising from the active greenschist facies metamorphic zone and transporting gold released during rock recrystallisation. Metamorphic fluid flow at the Pingfengshan historic gold mine was focussed in well-defined (4 km3) fracture zones with networks of quartz veins, whereas large surrounding volumes of rock are largely unveined. Gold and arsenopyrite occur in several superimposed vein generations, with ankeritic alteration of host rocks superimposed on chlorite–calcite alteration zones as fluids cooled and became out of equilibrium with the host rocks. Mineralising fluids had δ18O near +10‰, δ13C was between −1‰ and −6‰ and these fluids were in isotopic equilibrium with host rocks at ∼350°C. Ankeritic veins were emplaced in extensional sites in kink fold axial surfaces, formed as the rock mass was transported laterally from compressional to extensional regimes in the orogen. Rapid exhumation (>2 mm/year) of the Slate Belt is causing a widespread shallow conductive thermal anomaly without igneous intrusions. Meteoric water is penetrating into the conductive thermal anomaly to contribute to crustal fluid flow and generate shallow boiling fluids (∼250°C) with fluid temperature greater than rock temperature. The meteoric-hydrothermal system impinges on, but causes only minor dilution of, the gold mineralisation system at depth.  相似文献   

20.
Mineral transformation of host rocks and localization of orebodies at the unconformity-type uranium deposits are considered for the Karku deposit in the northern Ladoga region. It is shown that the great depth of uranium mineral formation and the peculiar composition of host rocks, along with temperature and chemistry of fluids, played a critical role in variation of lithostatic and fluid pressure, porosity, and permeability. The compaction of quartz sandstone and gravelstone, which are typical host rocks at unconformity-type deposits, the development of microstylolithic sutures, conformal structures, pressure solution and deposition of quartz in free pores gave rise to the closure or constraint of pore space and to increase in pore pressure of fluids in the deep part of the Riphean troughs with approaching lithostatic loading. A transitional zone between hydrostatic and lithostatic pressure controlled localization of orebodies and was decisive for uranium mineral formation. This zone coincided with the Riphean-Paleoproterozoic unconformity and sank somewhat into the crystalline basement. Below this transitional zone, the intergranular fluid was under a pressure that was close to the pressure on solid phases, i.e., P tot ≈ P fl. The reliability of this phenomenon is confirmed by cessation of pressure solution-redeposition of quartz and distinct deceleration of dehydration of hydrous minerals. As is shown for the Karku deposit, the highly hydrated clay minerals of the illite-smectite series are widespread in its subore portion and lacking at the supraore levels along with termination of quartz regeneration. It is suggested that a zone of superhigh fluid pressure in deep parts of sedimentary basins constrains localization of uranium orebodies by structural and stratigraphic unconformity between Riphean and Paleoproterozoic rocks. It is stated that altered wall rocks at the unconformity-type uranium deposits cannot be identified with products of hydrothermal phyllic and argillic alteration of host rocks at the medium- and low-temperature endogenic deposits. The main distinctions consist in lack of wall-rock metasomatic reaction zoning and acid-alkaline evolution of solutions. All transformations of host rocks should be classified as diverse manifestations of deep catagenesis of sedimentary sequences and buried regolith. The carbon and oxygen isotopic compositions of calcite from host rocks at the Karku deposit are far from those of magmatic and hydrothermal carbonates. They are characterized by a high δ18O = +17 to +25‰ and a high dispersion of δ13C = −1.5 to almost −15‰. No granitoid magmatism is known in the regions, where the unconformity-type uranium deposits occur. Therefore, the rocks of the crystalline basement are the most probable source of uranium, which precipitated on the reductive barrier as a product of interaction with bitumen contained in the Riphean basal beds.  相似文献   

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