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1.
A large number of Variscan mesothermal gold deposits are located in the central part of the Bohemian Massif, close to the Central Bohemian Plutonic Complex. The Petrá)kova hora deposit has many features that distinguish it from other deposits in the region and suggest its mineralization is closely related to the late magmatic processes associated with the Petrá)kova hora granodiorite. The gold ores occur as sheeted arrays of quartz veins and veinlets hosted by the small Petrá)kova hora granodiorite stock. Gold is found mainly as free grains of >900 fineness, and is accompanied by abundant pyrrhotite and chalcopyrite, and accessory pyrite, arsenopyrite, loellingite, and molybdenite. Molybdenite from the Petrá)kova hora deposit has been dated by the Re-Os method at 344.4DŽ.8 Ma. Hydrothermal alteration in the Petrá)kova hora deposit exhibits a distinct temporal paragenesis. Selectively pervasive, early K-alteration and silicification are the oldest hydrothermal phases. These were followed by early quartz veins (Q1 to Q4) that contain most of the gold mineralization. Late quartz veins (Q5) and fracture-controlled silicification are gold-poor or barren. Barren calcite veins are the youngest hydrothermal product. Extensive low-temperature, meteoric-water dominated alteration, as is typical of classic porphyry deposits, is absent. However, the lower '18O whole rock values for Petrá)kova hora granodiorite and aplite (+2.4 to +5.1‰ SMOW) compared to other intrusions in the region reflect either interaction with isotopically light external fluids or magma assimilation of small volumes of hydrothermally altered country rock. The '18O isotopic compositions for quartz, scheelite and hornblende (7.7 to 13.4‰ SMOW) and the '34S compositions for sulfide minerals (-1 to +3.5‰ CDT) from early, gold-rich quartz veins indicate formation at high temperatures (590 to 400 °C) from fluids with a magmatic isotopic signature ('18OFLUID of 5.7 to 7.2‰). Fluids related to late quartz veins (Q5) suggest the presence of a significant component of non-magmatic water ('18OFLUID: +2.5 to +4.0‰). The '34S values of post-Q5 sulfide minerals (-4.5 to -3.5‰) reflect at least partial derivation of late-stage sulfur from a source external to the intrusions. Aqueous, aqueous-carbonic and nitrogen-bearing fluid inclusions were identified in hydrothermal and igneous quartz, with the aqueous inclusions being the most common. In hydrothermal vein quartz, the salinity of primary aqueous inclusions falls into ranges 6 to 23 and 33 to 41 equiv. wt% NaCl; in igneous quartz, populations in salinity were observed between 5 to 16, 35 to 40 and 62 to 70 equiv. wt% NaCl. The salt component of these fluids is best, and minimally, approximated by the NaCl-KCl-CaCl2 system. Low- and high-salinity aqueous-carbonic inclusions are accessory in many of the analyzed samples. Three large successive pulses of fluids are recognized. Each pulse begins with a high-salinity (>30 equiv. wt% NaCl) magmatic fluid and evolves toward a lower salinity (~5 equiv. wt% NaCl) fluid. Data suggest that external (meteoric?) water(s) were significant for only the third fluid pulse, which formed the late Q5 quartz veins and the calcite veins. Polyphase fluid inclusions hosted by igneous quartz of the Petrá)kova hora granodiorite indicate minimum trapping conditions of about 3 kbar and 550 °C. The gold-rich Q1 to Q4 veins may have formed along a quasi-isobaric cooling path at 2.5 to 1.5 kbar and 590 to 400 °C. This was followed by uplift, and formation of late Q5 quartz veins (0.5 to 1.5 kbar; ~300 °C) and post-ore calcite veins (<0.5 kbar; 100 to 140 °C). The characteristics of the Petrá)kova hora deposit suggest that it may represent a position intermediate between intrusion-related gold systems (e.g., Fort Knox deposit, Alaska) and gold-rich, copper-poor porphyry deposits (e.g., Maricunga Belt in Chile). As such, the Petrá)kova hora deposit might be an example of the reduced gold sub-type of porphyry deposit.  相似文献   

2.
The Mallery Lake area contains pristine examples of ancient precious metal-bearing low-sulfidation epithermal deposits. The deposits are hosted by rhyolitic flows of the Early Proterozoic Pitz Formation, but are themselves apparently of Middle Proterozoic age. Gold mineralization occurs in stockwork quartz veins that cut the rhyolites, and highest gold grades (up to 24 g/t over 30 cm) occur in the Chalcedonic Stockwork Zone. Quartz veining occurs in two main types: barren A veins, characterized by fine- to coarse-grained comb quartz, with fluorite, calcite, and/or adularia; and mineralized B veins, characterized by banded chalcedonic silica and fine-grained quartz, locally intergrown with fine-grained gold or electrum. A third type of quartz vein (C), which crosscuts B veins at one locality, is characterized by microcrystalline quartz intergrown with fine-grained hematite and rare electrum. Fluid inclusions in the veins occur in two distinct assemblages. Assemblage 1 inclusions represent a moderate temperature (Th=150 to 220 °C), low salinity (~1 eq. wt% NaCl, with trace CO2), locally boiling fluid; this fluid type is found in both A and B veins and is thought to have been responsible for Au-Ag transport and deposition. Assemblage 2 inclusions represent a lower temperature (Th=90 to 150 °C), high salinity calcic brine (23 to 31 wt% CaCl2-NaCl), which occurs as primary inclusions only in the barren A veins. Assemblage 1 and 2 inclusions occur in alternating quartz growth bands in the A-type veins, where they appear to represent alternating fluxes of dilute fluid and local saline groundwater. No workable primary fluid inclusions were observed in the C veins. The A-vein quartz yields '18O values from 8.3 to 14.5‰ (average=10.9ǃ.7‰ [1C], n=30), whereas '18O values for B-vein quartz range from 11.2 to 14.0‰ (average=13.0ǂ.9‰, n=12). Calculated '18OH2O values for the dilute mineralizing fluid from B veins range from -2.6 to 0.2‰ (average=-0.8ǂ.9‰, n=12) and are consistent with a dominantly meteoric origin. No values could be calculated for the brine, however, because all A-vein quartz samples contain mixed fluid inclusion populations. However, the fact that A-vein quartz samples extend to lower '18O values than the B veins suggests that the brine had a lighter isotopic signature relative to the dilute fluid. Hydrogen isotopic ratios of fluid inclusion waters extracted from eleven quartz samples of both vein types range from 'DFI=-56 to -134‰, but show no particular correlation with vein type. In most respects, the mineralogical and fluid characteristics of the Mallery Lake system are comparable to those of Phanerozoic low-sulfidation deposits, and although the presence of high salinity brines is unusual in such deposits, it is not unknown (e.g., Creede, Colorado). In addition, one of the few other examples of well-preserved, Precambrian, low-sulfidation epithermal deposits, from the Central Pilbara tectonic zone, Australia, contains a similarly bimodal fluid assemblage. The significance of these saline brines is not clear, but from this study we infer that they were not directly involved with Au-Ag transport or deposition.  相似文献   

3.
水力压裂角砾岩：一种重要的地质异常和找矿标志   总被引：1，自引：0，他引：1  
水力压裂作用是地壳内的一种重要变形破裂方式，许多热液脉体和热液矿床直接受其控制，以华南金银寨大型负矿床为例，详细介绍了水力压裂角砾岩和裂隙一脉的几何特征，鉴别标志和形成机制，水力压裂角砾岩不仅是一种重要的地质异常，而且常伴随不同程度的金属矿化而使之成为一种重要的矿化体和找矿标志。  相似文献   

4.
Porphyry Cu-Mo-Au mineralisation with associated potassic and phyllic alteration, an advanced argillic alteration cap and epithermal quartz-sulphide-gold-anhydrite veins, are telescoped within a vertical interval of 400-800 m on the northeastern margin of the Thames district, New Zealand. The geological setting is Jurassic greywacke basement overlain by Late Miocene andesitic-dacitic rocks that are extensively altered to propylitic and argillic assemblages. The porphyry Cu-Mo-Au mineralisation is hosted in a dacite porphyry stock and surrounding intrusion breccia. Relicts of a core zone of potassic K-feldspar-magnetite-biotite alteration are overprinted by phyllic quartz-sericite-pyrite or intermediate argillic chlorite-sericite alteration assemblages. Some copper occurs in quartz-magnetite-chlorite-pyrite-chalcopyrite veinlets in the core zone, but the bulk of the copper and the molybdenum are associated with the phyllic alteration as disseminated chalcopyrite and as molybdenite-sericite-carbonate veinlets. The advanced argillic cap has a quartz-alunite-dickite core, which is enveloped by an extensive pyrophyllite-diaspore-dickite-kaolinite assemblage that overlaps with the upper part of the phyllic alteration zone. Later quartz-sphalerite-galena-pyrite-chalcopyrite-gold-anhydrite-carbonate veins occur within and around the margins of the porphyry intrusion, and are associated with widespread illite-carbonate (argillic) alteration. Multiphase fluid inclusions in quartz stockwork veins associated with the potassic alteration trapped a highly saline (50-84 wt% NaCl equiv.) magmatic fluid at high temperatures (450 to >600 °C). These hypersaline brines were probably trapped at a pressure of about 300 bar, corresponding to a depth of 1.2 km under lithostatic conditions. This shallow depth is consistent with textures of the host dacite porphyry and reconstruction of the volcanic stratigraphy. Liquid-rich fluid inclusions in the quartz stockwork veins and quartz phenocrysts trapped a lower salinity (3-20 wt% NaCl equiv.), moderate temperature (300-400 °C) fluid that may have caused the phyllic alteration. Fluid inclusions in the quartz-sphalerite-galena-pyrite-chalcopyrite-gold-anhydrite-carbonate veins trapped dilute (1-3 wt% NaCl equiv.) fluids at 250 to 320 °C, at a minimum depth of 1.0 km under hydrostatic conditions. Oxygen isotopic compositions of the fluids that deposited the quartz stockwork veins fall within the 6 to 10‰ range of magmatic waters, whereas the quartz-sulphide-gold-anhydrite veins have lower '18Owater values (-0.6 to 0.5‰), reflecting a local meteoric water (-6‰) influence. A '18O versus 'D plot shows a trend from magmatic water in the quartz stockwork veins to a near meteoric water composition in kaolinite from the advanced argillic alteration. Data points for pyrophyllite and the quartz-sulphide-gold-anhydrite veins lie about midway between the magmatic and meteoric water end-member compositions. The spatial association between porphyry Cu-Mo-Au mineralisation, advanced argillic alteration and quartz-sulphide-gold-anhydrite veins suggests that they are all genetically part of the same hydrothermal system. This is consistent with K-Ar dates of 11.6-10.7 Ma for the intrusive porphyry, for alunite in the advanced argillic alteration, and for sericite selvages from quartz-gold veins in the Thames district.  相似文献   

5.
The Dafulou and Huile vein and stratabound cassiterite-sulfide deposits and sheeted ore veins at the Kangma cassiterite-sulfide deposit are located in the eastern part of the Dachang tin field. These deposits are hosted in a sedimentary sequence containing significant concentrations of organic matter in the form of Lower Devonian calcareous black shales and hornfels. These rocks together with the younger intrusion of Longxianggai granite (91DŽ Ma) actively participated in the formation of Sn-polymetallic deposits. The following three major stages have been distinguished in stratiform and vein-type orebodies at Dafulou, Huile and Kangma: stage I (cassiterite, pyrrhotite, arsenopyrite, tourmaline, carbonate), stage II - main sulfide stage (quartz, cassiterite, arsenopyrite, pyrrhotite, sphalerite, stannite, pyrite, carbonates) and stage III (native Bi, galena, electrum, sulfosalts). Stage IV (post-ore), recognized at Huile is represented by barren carbonates and zeolites. Whole rock geochemistry has revealed that at Dafulou, Bi and Cu correlate strongly with S, whereas V and Pb correlate well with Corg (organic carbon). The similar distribution patterns of selected elements in average slightly mineralized low-Ca black shales indicate a fluid composition similar for all deposits studied. Studies of graphitization of the organic matter in black shales adjacent to orebodies indicate that d(002) and FWHM (full width in half maximum)/peak height values gradually decrease in the following sequence: Dafulou deposit M Kangma deposit M Huile deposit. The pyrolysate of wall rocks at the Dafulou deposit is relatively enriched in asphaltenes and maltenes (55.6-72.0% of the pyrolysate) comparable with pyrolysate obtained from more distal black shales (19.2-28.5%). Typical GC-MS spectra of pyrolysate from distal black shales are dominated by alkanes in the n-C15 to n-C25 range, aromatic molecules being represented mostly by alkyl-naphthalenes. In contrast, only traces of aliphatic hydrocarbons in the n-C14 to n-C18 range and elemental sulfur were identified in pyrolysates from pyrrhotitized wall rocks. The earliest fluid inclusions of the studied system occur in the quartz-tourmaline-cassiterite assemblage of stage I at Dafulou. These inclusions are H2O-CO2-CH4-rich, with 10 to 20 vol% of aqueous phase. P-T conditions of the trapping of inclusions are estimated to be up to 400 °C and 1.3 to 2.0 kbar (between 5.0 and 7.5 km under lithostatic pressure). In contrast, the presence of a low density gaseous CO2-CH4 phase indicates relatively low pressures during the formation of the breccia-type quartz-calcite-cassiterite-sulfide mineralization (stage II), when P-T conditions probably reached approx. 380 to 400 °C and 0.6 kbar (up to 6 km under hydrostatic pressure). Fluid inclusion data and oxygen isotope thermometry indicate that cassiterite-sulfide ores of the main sulfide stage (stage II) formed from aqueous-carbonic fluid (CO2/CH4 =ᄺ) at temperatures of up to 390 °C at Dafulou and in a temperature range of 250 to 360 °C at Huile and 260 to 370 °C at Kangma. The '34S values of sulfides from Dafulou range mostly between -1 and -6‰, whereas sulfides from the Kangma and Huile deposits are characterized by more negative '34S values (between -8 and -11‰, and between -9 and -12‰, respectively). These data suggest that bacteriogenic sulfides of black shales were a dominant source of reduced sulfur for epigenetic (vein and replacement) mineralization. Oxygen isotopic compositions of five quartz-cassiterite pairs from Dafulou and Huile show a relatively narrow range of calculated oxygen isotope temperatures (250-320 °C, using the equation of Alderton 1989) and high '18Ofluid values between +8 and +10‰ (SMOW), which are in agreement with fluid derivation from and/or high temperature equilibration with the Longxianggai granite. The carbon and oxygen isotope composition of carbonates reflects variable carbon sources. Stage I calcite is characterized by narrow ranges of '13C (-7.0 to -9.5‰ PDB) and '18O (+15.0 to +17.5‰ SMOW). This calcite shows ubiquitous deformation, evidenced by intense development of twins. Fluid compositions calculated at 330 °C for the Dafulou and Huile deposits and at 270-300 °C for the Kangma deposit ('18Ofluid between +10.0 and +11.5‰ SMOW, '13Cfluid between -5.5 and -7.5‰ PDB), agree with fluid derivation from and/or equilibration with the peraluminous, high-'18O Longxianggai granite and suggest a significant influence of contact metasedimentary sequences (carbon derived from decomposition and/or alteration of organic matter of calcareous black shales). The '13 C values of organic matter from the Lower to Upper Devonian host rocks at the Dafulou deposit (-24.0 and -28.0‰) fit with a marine origin from algae. However, organic matter adjacent to the host rock-ore contact displays a slight enrichment in 13C. The organic carbon from the Huile and Kangma deposits is even more 13C enriched (-24.6 to -23.5‰). The most heavy '13 C values (-16.5‰) were detected in hornfels sampled at the contact of the Upper Devonian sediments with the Longxianggai granite. The '13C data broadly correlate with the degree of structural ordering (degree of graphitization) of organic matter, which indicates that both variables are related to thermal overprint.  相似文献   

6.
Syntectonic hydrothermal Pb-Zn vein systems of the Ramsbeck deposit, Germany, have been extensively overprinted by late-stage fluids responsible for fissure vein mineralisation. This has caused remobilisation of vein components, notably of sphalerite and galena, as well as the formation of various Sb sulphosalt minerals, including boulangerite, semseyite, tetrahedrite and bournonite. A detailed sulphur isotope study of sphalerite, galena and sulphosalts related to different stages of recrystallisation, remobilisation and reaction has been carried out using an insitu laser combustion technique. Primary sphalerite-galena ores from flat-lying thrust zones are characterised by homogeneous positive '34S values in the range +6.5 to +7.7‰. In contrast, recrystallised and remobilised sphalerite and galena from both overprinted thrust zones and extensional fissure veins show '34S values in the range -1.1 to +2.9‰ and -0.7 to +8.7‰ respectively. Sulphosalt minerals show a similar variation in their sulphur isotope compositions, which range between -1.7 and +7.7‰. Fissure vein hosted sphalerite and sulphosalts display significantly more negative '34S values than the primary Pb-Zn ores. Sphalerite which recrystallised in situ and boulangerite which formed by reactive replacement of primary galena show slightly more positive '34S values than fissure vein hosted minerals. The compositional range of remobilised mineral phases can be best explained by varying contributions (variable mixing) of sulphur derived from (1) the primary sphalerite-galena ores of the flat thrust systems, and (2) the hydrothermal fluid responsible for the fissure vein mineralisation. Equilibrium fractionation temperatures calculated for sphalerite-galena pairs contrast strongly with fluid inclusion data. Isotopic fractionation related to the remobilisation has to be interpreted in terms of kinetic processes.  相似文献   

7.
A fossil wood cell texture with pitchblende and coffinite found at a sandstone-hosted roll-type uranium deposit, Xinjiang, NW China, is first reported here for the country. In the mineralized sandstone, detrital grains consisting of quartz, feldspar, rock fragments, carbonaceous trashes, mica and accessory minerals were deposited in early Turassic time and were cemented by clays and minor authigenic calcite and quartz. Pitchblende and minor coffinite are principal ore minerals at the deposit, and selectively replaced carbonized fossil wood remnants or filled fossil wood cells. An excellent fossil wood cell texture with primary uranium minerals formed. Replacement of organic debris by primary uranium minerals may be due to a local reducing environment resulting from the production of CH4, H2S or H2SO3 in its decomposition, and a biochemical reaction indicated by the common presence of framboidal pyrite.  相似文献   

8.
The Don Sixto mining area in Mendoza province, central‐western Argentina, contains an epithermal low sulfidation Au–Ag deposit. It is a small deposit (～4 km2), with a gold resource of 36 t. In Don Sixto, ore minerals are disseminated in the hydrothermal quartz veins and hydrothermally altered volcanic‐pyroclastic rock units of Permian–Triassic age. On the basis of the texture, ore mineral paragenesis and cross cutting relationship of gangue minerals, seven stages of mineralization were recognized and described. The first six stages are characterized by quartz veins with minor amounts of base metal minerals and the last stage is represented by fluorite veins with minimal quantities of base metal minerals; the precious metal mineralization is mainly related to the fourth stage. The hydrothermal veins exhibit mainly massive, crustiform and comb infilling textures; the presence of bladed quartz replacement textures and quartz veins with adularia crystals are indicative of boiling processes in the system. Fluid inclusion and complementary stable isotope studies were performed in quartz, fluorite, and pyrite samples from the vein systems. The microthermometric data were obtained from primary, biphasic (liquid‐vapor) fluid inclusion assemblages in quartz and fluorite. The maximum values for salinity and homogenization temperature (Th) came from the stage IV where quartz with petrographic evidence of boiling has average values of 4.96 wt% NaClequiv. and 286.9°C respectively. The lower values are related to the last stage of mineralization, where the fluid inclusions in fluorite have average salinities of 1.05 wt% NaClequiv. and average homogenization temperatures of 173.1°C. The oxygen and sulfur isotopic fractionation was analyzed in quartz and pyrite. The calculated isotopic fractionation for oxygen in the hydrothermal fluid is in the range of δ18OH2O = ?6.92 up to ?3.08‰, which indicates dominance of a meteoric source for the water, while sulfur reaches δ34SH2S = 1.09‰, which could be reflecting a possible magmatic, or even a mixed source.  相似文献   

9.
Sparry and microcrystalline magnesite are minor constituents of the Upper Triassic Burano Evaporite Formation of the northern Apennines in Italy. Petrography and geochemistry of magnesite suggest three modes of formation. (1) Evaporitic precipitation of stratified microcrystalline magnesite layers associated with sulfate and carbonate rocks. Most REE are below ICP-MS detection limits. '18O is +20.2‰ (SMOW) and '13C is -2.6‰ (PDB). (2) Hydrothermal infill of Fe-rich (9.78 wt% FeO) lenticular sparry magnesite. This type of magnesite is characterized by very low LREE concentrations, whereas HREEs are relatively high. The fluid inclusion composition is NaCl-MgCl2-H2O, salinity is ~30 wt% NaCl equiv., and total homogenization temperatures range from 204-309 °C; '18O is +17.5‰ and '13C is +1‰. (3) The partial or total replacement of dolostones by lenticular sparry magnesite. LREEs are lower in magnesite compared with the partly replaced dolostones. Magnesite yields '18O and '13C compositions of +17.3 to +23.6‰ and +0.5 to +1.4‰, respectively, whereas the partly replaced dolostones yield '18O and '13C values of +25.0 to +26.2 and +1.3 to +1.9, respectively. Complete replacement of dolostones produced massive lenticular sparry magnesite rock containing ooids and axe-head anhydrite relicts; LREEs are depleted compared to unaffected dolostones; '18O and '13C compositions range from +16.4 to +18.4‰ and +0.4 to +0.9‰, respectively. These data and the association between fracture-filling and replacive magnesite suggests a metasomatic system induced by hydrothermal circulation of hot and saline Mg-rich fluids. These processes probably occurred in the Oligocene-Miocene, when the Burano Formation acted as main detachment horizon for the Tuscan Nappe during the greenschist facies metamorphism of the Apuane complex. Thrusting over the Apuane zone produced large scale fluid flow focused at the Tuscan Nappe front. Sources of Mg-rich fluids were metamorphic reactions in the Apuane complex and dissolution of Mg-salts at the thrust front. Considering a maximum tectonic burial depth of 10 km, as inferred from the geometry of the chain, the pressure-corrected temperature of magnesite precipitation (380 to 400 °C) and the calculated fluid composition ('18O=+13.3ǃ.2‰) are in the range of the published Apuane metamorphic temperatures (300-450 °C) and fluid compositions ('18O=7-16‰). The results of this study support the hydrothermal-metasomatic model for the formation of sparry magnesite deposits at the expense of dolostone units involved in thrusting and low-grade metamorphism, as proposed for the Northern Graywacke Zone (Alps) and the Eugui deposit (western Pyrenees).  相似文献   

10.
西藏昂仁县罗布真金银矿位于冈底斯成矿带西段,其大地构造位置属于南拉萨微陆块,矿体受北西西的断裂构造控制,呈脉状、透镜状产于始新世帕那组火山岩中。按照矿石工业类型分类,矿石类型可分为角砾岩型、石英脉型和蚀变岩型等三类,主要金银矿石矿物为自然金和碲银矿等。矿区广泛繁育不同特征的热液脉体,通过系统的野外观测以及全面的岩相学研究,依据矿物共生组合、脉体切穿关系及蚀变特征,将热液脉体从早到晚划分为石英-黄铁矿阶段(S1)的石英-黄铁矿大脉、玉髓华石英-金-多金属硫化物阶段(S2)的石英-金属硫化物网脉、石英-碳酸盐矿物阶段(S3)的石英-方解石细脉。罗布真金银矿床热液脉体主要发育气液两相流体包裹体(富液两相包裹体、富气两相包裹体)和含子矿物(碳酸盐矿物)三相流体包裹体。本文在野外地质调查的基础上,对不同成矿阶段的石英脉进行了流体包裹体的岩相学观测、显微测温、成分分析以及H-O同位素测试。S1阶段流体包裹体的形成温度集中在310~330 ℃,盐度(w(NaCleq))集中在5.0%~10.1%,密度介于0.60~0.80 g/cm3;S2阶段流体包裹体的形成温度集中在240~280 ℃,盐度介于3.0%~7.0%,密度介于0.70~0.90 g/cm3;S3阶段流体包裹体的形成温度集中在121~215 ℃,盐度集中在1.0%~5.0%,密度集中在0.85~1.00 g/cm3。拉曼分析表明,罗布真金银矿的流体包裹体成分以H2O为主,并含有少量的CO2、N2、CH4等气体及方解石子晶。各热液脉体石英中流体包裹体的δ${{\text{D}}_{{{\text{H}}_{2}}\text{O},\text{V-SMOW}}}$值的变化范围为-106.1‰~-97.5‰,δ18${{\text{O}}_{{{\text{H}}_{2}}\text{O},\text{V-SMOW}}}$值的变化范围为-7.33‰~-7.13‰,展示其成矿流体主要源自火山岩围岩中的循环地下水,在早阶段还有少量岩浆水的加入。成矿流体在岩浆作用驱动下,沿着断裂从深部封闭体系运移到浅部的开放体系,迅速突破临界状态减压沸腾并产生相分离导致金属硫化物沉淀,形成矿化。随着含矿热液成矿物质及金属硫化物的大量析出,流体温度、盐度迅速降低,金属矿物成矿作用随之结束。罗布真金银矿床的成矿流体为中低温、低盐度、中低密度并含有少量CO2、N2、CH4等气体的流体,具有典型的浅成低温热液矿床成矿流体的特征。  相似文献   

11.
Uranium deposits containing molybdenum and fluorite occur in the Central Mining Area, near Marysvale, Utah, and formed in an epithermal vein system that is part of a volcanic/hypabyssal complex. They represent a known, but uncommon, type of deposit; relative to other commonly described volcanic-related uranium deposits, they are young, well-exposed and well-documented. Hydrothermal uranium-bearing quartz and fluorite veins are exposed over a 300 m vertical range in the mines. Molybdenum, as jordisite (amorphous MoS2), together with fluorite and pyrite, increase with depth, and uranium decreases with depth. The veins cut 23-Ma quartz monzonite, 20-Ma granite, and 19-Ma rhyolite ash-flow tuff. The veins formed at 19-18 Ma in a 1 km2 area, above a cupola of a composite, recurrent, magma chamber at least 24 × 5 km across that fed a sequence of 21- to 14-Ma hypabyssal granitic stocks, rhyolite lava flows, ash-flow tuffs, and volcanic domes. Formation of the Central Mining Area began when the intrusion of a rhyolite stock, and related molybdenite-bearing, uranium-rich, glassy rhyolite dikes, lifted the fractured roof above the stock. A breccia pipe formed and relieved magmatic pressures, and as blocks of the fractured roof began to settle back in place, flat-lying, concave-downward, “pull-apart” fractures were formed. Uranium-bearing, quartz and fluorite veins were deposited by a shallow hydrothermal system in the disarticulated carapace. The veins, which filled open spaces along the high-angle fault zones and flat-lying fractures, were deposited within 115 m of the ground surface above the concealed rhyolite stock. Hydrothermal fluids with temperatures near 200 °C, 18OH2O∼−1.5, DH2O∼−130, log f O2 about −47 to −50, and pH about 6 to 7, permeated the fractured rocks; these fluids were rich in fluorine, molybdenum, potassium, and hydrogen sulfide, and contained uranium as fluoride complexes. The hydrothermal fluids reacted with the wallrock resulting in precipitation of uranium minerals. At the deepest exposed levels, wallrocks were altered to sericite; and uraninite, coffinite, jordisite, fluorite, molybdenite, quartz, and pyrite were deposited in the veins. The fluids were progressively oxidized and cooled at higher levels in the system by boiling and degassing; iron-bearing minerals in wall rocks were oxidized to hematite, and quartz, fluorite, minor siderite, and uraninite were deposited in the veins. Near the ground surface, the fluids were acidified by condensation of volatiles and oxidation of hydrogen sulfide in near-surface, steam-heated, ground waters; wall rocks were altered to kaolinite, and quartz, fluorite, and uraninite were deposited in veins. Secondary uranium minerals, hematite, and gypsum formed during supergene alteration later in the Cenozoic when the upper part of the mineralized system was exposed by erosion. Received: 23 June 1997 / Accepted: 15 October 1997  相似文献   

12.
661铀矿床流体包裹体特征及成矿流体来源探讨   总被引：2，自引：0，他引：2  
本文利用显微测温学和激光喇曼光谱方法,研究了661铀矿床与铀成矿作用有关的脉石矿物(萤石、石英和方解石)中的流体包裹体。结果表明,成矿早期脉石矿物中的流体包裹体均一温度为130~250℃,盐度为1.65%~3.44%(NaCl),密度为0.81~1.01 g/cm3;成矿晚期流体包裹体的均一温度为95~150℃,盐度为1.48%~1.64%(NaCl),密度为0.88~0.96g/cm3。这些资料揭示出该矿床的成矿流体为中低温、低盐度、中等密度热液。激光喇曼光谱气相成分分析主要为H2O,未见其他气体成分。明显不同于岩浆热液矿床中的包裹体特征及其成矿流体的性质,结合该矿床成矿地质特征、氧同位素及区域铀矿床成矿物化条件等资料,进一步分析推断成矿流体的水可能主要来自大气降水。  相似文献   

13.
The metalized quartz veins is located 5 km west of the Iraqi-Iran border in the Qandil range. The quartz veins included sulfide and oxide ore minerals which mostly occur in the form of open-space filling texture. The polymetallic mesothermal quartz veins are hosted by marble and phyllite rocks. Within these veins, multiphase, open-space filling and crustiform, bedding to massive textures with pyrite, sphalerite, galena, chalcopyrite,galena, sphalerite, tenorite, azurite, and malachite are observed. Selected samples were analyzed by using ore microscopy and electron probe micro analyzer (EPMA) and scanning electron microscope (SEM). Ore minerals show replacement textures. The paragenesis diagram was made from a careful study of polished sections and three stages have been identified including pre-stage mineralization, mineralization, and post-mineralization stages.Fluid inclusion microthermometric analysis of 15 primary inclusions of quartz veins indicated that ore mineralization at the studied area were formed by a mesothermal, low to medium density, and dilute NaCl-type fluid system. The source of the fluid is mostly metamorphic which became mixed with other fluids later. Hydrothermal fluids of the selected studied area were classified into two groups based on microthermometry study; the first group had a higher homogenization temperature (335.5 to 386.8 °C) than the second group (194.1 to 298.5 °C), with a small difference in salinity between them. Nearly each group has different complexes including chloride and sulfide complexes respectively. The results of stable sulfur isotope of the ore minerals (chalcopyrite and sphalerite) confirmed the sedimentary and/or metamorphic origin of the ore mineralization.  相似文献   

14.
Abstract. Denggezhuang gold deposit is an epithermal gold‐quartz vein deposit in northern Muru gold belt, eastern Shandong, China. The deposit occurs in the NNE‐striking faults within the Mesozoic granite. The deposit consists of four major veins with a general NNE‐strike. Based on crosscutting relationships and mineral parageneses, the veins appear to have been formed during the same mineralization epochs, and are further divided into three stages: (1) massive barren quartz veins; (2) quartz‐sulfides veins; (3) late, pure quartz or calcite veinlets. Most gold mineralization is associated with the second stage. The early stage is characterized by quartz, and small amounts of ore minerals (pyrite), the second stage is characterized by large amounts of ore minerals. Fluid inclusions in vein quartz contain C‐H‐O fluids of variable compositions. Three main types of fluid inclusions are recognized at room temperature: type I, two‐phase, aqueous vapor and an aqueous liquid phase (L+V); type II, aqueous‐carbonic inclusions, a CC2‐liquid with/without vapor and aqueous liquid (LCO2+VCC2+Laq.); type III, mono‐phase aqueous liquid (Laq.). Data from fluid inclusion distribution, microthermometry, and gas analysis indicate that fluids associated with Au mineralized quartz veins (stage 2) have moderate salinity ranging from 1.91 to 16.43 wt% NaCl equivalent (modeled salinity around 8–10 wt% NaCl equiv.). These veins formatted at temperatures from 80d? to 280d?C. Fluids associated with barren quartz veins (stage 3) have a low salinity of about 1.91 to 2.57 wt% NaCl equivalent and lower temperature. There is evidence of fluid immiscibility and boiling in ore‐forming stages. Stable isotope analyses of quartz indicate that the veins were deposited by waters with δO and δD values ranging from those of magmatic water to typical meteoric water. The gold metallogenesis of Muru gold belt has no relationship with the granite, and formed during the late stage of the crust thinning of North China.  相似文献   

15.
The Utanobori gold deposit is a low‐sulfidation, epithermal vein‐type deposit located in northern Hokkaido, Japan. The deposit is hosted by conglomerate, sandstone, and tuff of the Middle to Late Miocene Esashi Formation. These rocks were hydrothermally altered. Silica sinters and quartz‐adularia veins are common in the deposit. The quartz‐adularia veins either contain a ginguro band, which corresponds to the main gold‐bearing vein (Type 1 Veins), or do not contain a ginguro band but contain minor adularia (Type 2 Veins). Type 1 Veins are divided into three stages with 12–14 substages. Ore minerals identified include electrum, naumannite, chlorargyrite, bromargyrite, an unidentified Fe‐Sb mineral, and an Fe‐(Sb)‐As mineral. These ore minerals formed in the main mineralization stages I (bands I‐b and I‐d) and II (band II‐a). Scanning electron microscopy with cathodoluminescence images show that cathodoluminescence‐dark microcrystalline quartz exhibiting colloform (ghost‐sphere) texture is closely associated with ore minerals in the Type 1 Vein and Type 2 Vein, and the Al and K contents of such quartz are commonly >1000 ppm. This indicates that the ore minerals were crystallized from alkaline, silica‐saturated fluids at temperatures <200°C, which initially deposited amorphous silica that was recrystallized to microcrystalline quartz. The average Au content of electrum is 52.5 at% Au (n = 10), 65.7 at% Au (n = 20), and 55.5 at% Au (n = 5) in bands I‐b, I‐d, and II‐a, respectively, of Type 1 Veins. The δ34SCDT values of two fine‐grained disseminated pyrites in the altered conglomerate and bedded tuff in the argillic altered zone are ?4.3 and ?4.2‰. Ar‐Ar dating on adularia yielded 13.6 ± 0.06 Ma, 13.6 ± 0.07 Ma, and 13.6 ± 0.06 Ma for the stages I, II, and III of the Type 1 Vein, respectively. K‐Ar ages determined on adularia in the silica sinter and on whole‐rock of glassy rhyolite of the Esashi Formation are 15.0 ± 0.4 Ma and 14.6 ± 0.4 Ma, respectively. These radiometric ages indicate that silica sinter associated with the rhyolitic volcanic rocks formed prior to the main gold mineralization.  相似文献   

16.
广东长排铀矿床成矿流体特征   总被引：1，自引：0，他引：1  
长排铀矿床位于广东长江铀矿田内,矿体主要赋存在北北西向硅化断裂带内及其两侧的蚀变花岗岩中。流体包裹体显微测温和激光拉曼光谱分析表明,成矿流体为中低温、中低盐度的含CO2、CH4和H2的流体。铀成矿期流体包裹体均一温度多集中于120~250 ℃,盐度为04%~102%。氢、氧同位素分析表明,成矿流体可能来源于深部,后期有大气降水的加入。成矿期方解石的δ13C值大多数集中于-91‰~-82‰,以深源碳为主。综合分析认为,长排铀矿床属于中低温热液脉型铀矿床。成矿流体经历了沸腾作用,使CO2等挥发分逃逸,这可能是长排铀矿床铀矿沉淀、富集的主要原因。  相似文献   

17.
The Au-Ag (-Pb-Zn) Apacheta deposit is located in the Shila district, 600 km southeast of Lima in the Cordillera Occidental of Arequipa Province, southern Peru. The vein mineralization is found in Early to Middle Miocene calc-alkaline lava flows and volcanic breccias. Both gangue and sulfide mineralization express a typical low-sulfidation system; assay data show element zoning with base metals enriched at depth and higher concentrations of precious metals in the upper part of the veins. Three main deposition stages are observed: (1) early pyrite and base-metal sulfides with minor electrum 1 and acanthite; (2) brecciation of this mineral assemblage and cross-cutting veinlets with subhedral quartz crystals, Mn-bearing calcite and rhombic adularia crystals; and finally (3) veinlets and geodal filling of an assemblage of tennantite/tetrahedrite + colorless sphalerite 2 + galena + chalcopyrite + electrum 2. Fluid inclusions in the mineralized veins display two distinct types: aqueous-carbonic liquid-rich Lw-c inclusions, and aqueous-carbonic vapor-rich Vw-c inclusions. Microthermometric data indicate that the ore minerals were deposited between 300 and 225 °C from relatively dilute hydrothermal fluids (0.6-3.4 wt% NaCl). The physical and chemical characteristics of the hydrothermal fluids show a vertical evolution, with in particular a drop in temperature and a loss of H2S. The presence of adularia and platy calcite and of co-existing liquid-rich and vapor-rich inclusions in the ore-stage indicates a boiling event. Strong H2S enrichment in the Vw-c inclusions observed at -200 m, the abundance of platy calcite, and the occurrence of hydrothermal breccia at this level may indicate a zone of intense boiling. The vertical element zoning observed in the Apacheta deposit thus seems to be directly related to the vertical evolution of hydrothermal-fluid characteristics. Precious-metal deposition mainly occurred above the 200-m level below the present-day surface, in response to a liquid/vapor phase separation due to an upward boiling front.  相似文献   

18.
Metamorphic isograds and time-integrated fluid fluxes were mappedover the 1500 km2 exposure of the Waits River Formation, easternVermont, south of latitude 4430'N. Isograds based on the appearanceof oligoclase, biotite, and amphibole in metacarbonate rocksdefine elongated metamorphic highs centered on the axes of twolarge antiforms. The highest-grade isograd based on the appearanceof diopside is closely associated spatially with synmetamorphicgranitic plutons. Pressure, calculated from mineral equilibria,was fairly uniform in the area, 7 1.5 kb; calculated temperatureincreases from {small tilde} 480C at the lowest grades in thearea to {small tilde} 575C in the diopside zone. CalculatedXco2f equilibrium metamorphic fluid increases from <0-03at the lowest grades to 0.2 in the amphibole zone and decreasesto 0.07 in the diopside zone. Time-integrated fluid fluxesincrease with increasing metamorphic grade, with the followingmean values for each metamorphic zone (in cm3/cm2): ankerite-oligoclasezone, 1 x 104; biotite zone, 7 x 104; amphibole zone, 2 x 105;diopside zone, 7 x 105. The mapped pattern of time-integrated fluxes delineates twolarge deep-seated ({small tilde} 25-km depth) regional metamorphichydrothermal systems, each centered on one of the major antiforms.Fluid flowed subhorizontally perpendicular to the axis of theantiforms from their low-temperature flanks to their hot axialregions and drove prograde decarbonation reactions as they went.Along the axes of the antiforms fluid flow was further focusedaround synmetamorphic granitic intrusions. In the hot axialregion fluid changed direction and flowed subvertically outof the metamorphic terrane, precipitating quartz veins. Estimatesof the total recharge, based on progress of prograde decarbonationreactions, nearly match estimates of the total discharge, basedon measured quartz vein abundance, (2-10) x 1012 cm3 fluid percm system measured parallel to the axes of the antiforms. Withinthe axial regions fluids had lower XCO2 and rocks record greatertime-integrated fluxes close to the intrusions than at positionsmore than {small tilde} 5 km from them. The differences in bothfluid composition and time-integrated flux can be explainedby mixing close to the intrusions of regional metamorphic fluidsof XCO2/ with fluids from another source with XCO2{small tilde}0 in the approximate volume ratio of 1:2.  相似文献   

19.
Gold mineralization of the Hutti mine, southern India, is situated in closely spaced laminated quartz veins and associated alteration haloes along steeply dipping shear zones within a sequence of rather uniform amphibolites. Intense shearing has resulted in large-scale mylonitization of the wall rocks. Anastomosing shear zones, with intervening lensoid bodies of unsheared amphibolites, are characteristic features of the deposit. The general pattern of symmetrical alteration comprises a distal zone of chlorite-rich rock, with a proximal biotite-rich zone adjacent to laminated quartz veins. Arsenopyrite thermometry yielded a temperature range of 350-477 °C for the biotite alteration zone, which preceded the formation of the laminated quartz veins. Mass balance calculations on the alteration zones indicate a gradual mass and volume loss during alteration. The alteration is accompanied by intense potash metasomatism and addition of sulfur, which resulted in the formation of arsenopyrite, pyrrhotite, and pyrite. Results of fluid inclusion studies suggest that low salinity (3.9-13.5 wt% NaCl equivalent) H2O-CO2 rich fluids were responsible for gold-rich laminated quartz vein formation in the Hutti deposit. These fluids constituted a later counterpart of the protracted fluid activity that first formed the biotite alteration zone. The estimated P-T values range from 1.0 to 1.7 kbar at 280-320 °C. These data, along with the alteration assemblages and the characteristic gold-sulfide association, both in the altered wall rock and laminated quartz veins, suggest that gold, transported as reduced bisulfide complexes, was deposited in response to sulfidation reactions in the wall rocks. Comparison of P-T conditions of formation of gold-quartz veins at Hutti with two other large gold deposits in the eastern Dharwar Craton, namely Kolar (1.8 kbar/280 °C) and western Ramagiri (1.45-1.7 kbar/240-270 °C), indicates broadly similar lode-gold forming conditions in the Dharwar Craton.  相似文献   

20.
The copper-rich, tourmaline-bearing Donoso breccia pipe is one among more than 15 different mineralized breccias in the giant (>50 million metric tonnes of copper) Miocene and Pliocene Río Blanco-Los Bronces copper deposit in the high Andes of central Chile. This breccia pipe, bracketed in age between 5.2 and 4.9 Ma, has dimensions of 500 by 700 m at the current surface 3,670 m above sea level. Its roots have yet to be encountered, and it is >300 m in diameter at the depth of the deepest drill holes. The Donoso breccia is, for the most part, monolithic, containing clasts of the equigranular quartz monzonite pluton which hosts the pipe. It is matrix supported, with between 5 and 25% of the total rock volume consisting of breccia-matrix minerals, which include tourmaline, quartz, chalcopyrite, pyrite, specularite, and lesser amounts of bornite and anhydrite. An open pit mine, centered on this breccia pipe, has a current production of 50,000 tonnes of ore per day at an average grade of 1.2% copper, and copper grade in the breccia matrix is significantly higher. Measured '18O for tourmaline and quartz from the matrix of the Donoso breccia at different levels of the pipe range from +6.9 to +12.0‰, and measured 'D in tourmaline ranges from -73 to -95‰. Temperatures of crystallization of these minerals, as determined by the highest homogenization temperatures of highly saline fluid inclusions, range from 400 to >690°C. When corrected for these temperatures, the stable isotope data indicate that fluids from which these breccia-matrix minerals precipitated were magmatic, with '18O between +5.6 to +9.1‰ and 'D between -51 to -80‰. These isotopic data preclude participation of a significant amount of meteoric water in the formation of the Donoso breccia. They support a model in which brecciation is caused by expansion of magmatic fluids exsolved from a cooling pluton, and breccia-matrix minerals, including copper sulfides, precipitated from the same magmatic fluids responsible for brecciation. Sericitic alteration of clasts in the breccia was also caused by these magmatic fluids. Different types of fluid inclusions imply that several different magmatic fluids were involved in formation of the Donoso breccia. These include high-temperature, highly saline, non-boiling fluids, trapped in inclusions that homogenize by halite dissolution, which probably exsolved from a magma cooling under relatively high (>1 kbar) lithostatic pressure conditions, consistent with geologic constraints. Other high-temperature, highly saline fluids are trapped in inclusions that homogenize by vapor-bubble disappearance and are spatially associated with vapor-rich inclusions, suggesting either phase separation (boiling) or simultaneous separation of immiscible brine and vapor from a magma cooling at lower hydrostatic pressure conditions. Both types of high-temperature, highly saline fluids circulated intermittently, as pressure fluctuated between lithostatic and hydrostatic conditions because of episodes of sealing and rebrecciation.  相似文献   

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