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1.
Abstract, Results of a study of fluid inclusions in anhydrite from drill hole Y-6 in the Chicxulub crater, of northwestern Yucatan, Mexico, are reported in this work. The Chicxulub crater was formed at the Cretaceous-Tertiary boundary by a meteorite impact. The resulting ejection breccias are composed mostly of hydrothermally altered crystalline basement material. The mineral assemblage pyroxene + anhydrite + quartz is associated with the hydrothermal alteration. The analyzed fluid inclusions in the anhydrite show highly heterogeneous phase assemblages within the same crystal plane. Fluid inclusion types include liquid plus vapor inclusions (L+V), vapor-rich inclusions (V), and inclusions containing daughter crystals (L+V+S). The eutectic temperatures indicate a brine composition dominated by CaCl2-NaCl. Both the salinity and the homogenization temperatures show a wide range (from 3.6 to 23 wt% NaCl equivalent for the L+V inclusions, and 36 to 42 wt% NaCl equivalent for the L+V+S inclusions). The homogenization temperatures range from 100° to 500°C. These data represent cooling and boiling trends. We assume that the impact breccias were ejected at high temperature in an aqueous environment (above 500°C). This caused boiling of sea water and precipitation of anhydrite with its inclusions.  相似文献   

2.
Fluid inclusions in quartz were synthesized by the method of crack healing at 2 kbar and temperatures of 500, 700, 750, and 800°C from solutions containing sodium fluoride (±chloride). Critical phenomena occur in the saturated solution of NaF. Thermometric and cryometric measurements were carried out. Fluid interaciton with quartz was observed under all the parameters of our experiments with the formation of intermediate compounds, which were also sometimes trapped in inclusions. Based on the results of cryometric investigations of inclusions synthesized from solutions of different concentration, the solubility of NaF was estimated as 3.9 wt % at 500°C. It was shown that at temperatures higher than 700°C, heterogeneous entrapment occurred in most cases. Complex unmixing processes took place in the inclusions synthesized under the conditions of the upper heterogeneous region. All our observations suggest that coarse dispersed emulsions of two liquids exist in the upper heterogeneous region: an essentially aqueous phase and a water-rich silicate-dominated phase.At temperatures of 206–389°C, liquid immiscibility occurred in the presence of vapor, and three equilibrium noncrystalline (fluid) phases coexisted. Under the experimental conditions, the addition of NaCl to the fluidgenerating mixture did not exert a significant influence on the phase state of fluorine-bearing fluid.  相似文献   

3.
The mobility of H2O and D2O by diffusion through quartz is illustrated with H2O-rich fluid inclusions synthesized at 600 °C and 337 MPa, within the α-quartz stability field. Inclusions are re-equilibrated at the same experimental conditions within a pure D2O fluid environment. Consequently, a gradient in volatile fugacities is the only driving force for diffusion, in the absence of pressure gradients and deformation processes. Up to 100 individual inclusions are analyzed in each experiment before and after re-equilibration by microscopic investigation, microthermometry, and Raman spectroscopy. Changes in fluid inclusion composition are obtained from the ice-melting temperatures, and density changes are obtained from total homogenization temperatures. After 1-day re-equilibration, inclusions already contain up to 11 mol % D2O. A maximum concentration of 63 mol % D2O is obtained after 40-day re-equilibration. D2O concentration profiles in quartz are determined from the concentration in inclusions as a function of their distance to the quartz surface. These profiles illustrate that deep inclusions contain less D2O than shallow inclusions. At equal depths, a variety of D2O concentration is observed as a function of fluid inclusion size: Small inclusions are stronger effected compared with large inclusions. A series of 19-day re-equilibration experiments are performed at 300, 400, 500, and 600 °C (at 337 MPa), at the same conditions as the original synthesis. The threshold temperature of diffusion is estimated around 450 °C at 337 MPa, because D2O is not detected in inclusions from re-equilibration experiments at 300 and 400 °C, whereas maximally 26 mol % D2O is detected at 500 °C. Our study indicates that the isotopic composition of natural fluid inclusions may be easily modified by re-equilibration processes, according to the experimental conditions at 600 °C and 337 MPa.  相似文献   

4.
The paper reports the results obtained by the detailed studying of carbonado (the first find in a gold placer in Primorie) and a collection of diamonds that was confiscated in 1937 from a poaching small digger and was kept safe at the Nezametnyi mine (near the village of Vostretsovo), which had developed this placer deposit. In the concentrate from the placer, carbonado is associated with green corundum, various ilmenite, zircon titanian amphiboles and pyroxenes, rutile, anatase, and fragments of subvolcanic biotite picrites. All of these minerals, native aluminum, and tin occur as inclusions in the diamonds. The carbonado from Primorie was determined to be practically identical to this mineral from Brazil, has a porous structure, is characterized by orange luminescence, contains inclusions of Y, Ce, La, Ba, and Sr phosphates, and has an isotopically light composition of its carbon (13C from ?25 to ?32‰). Pores of the carbonado aggregates contain clusters of diamond crystals. The collection of diamonds from an unknown source included six gem-quality transparent crystals, one rounded ballas, two cuboctahedral crystals (one of greenish and the other of silver-gray color, both with outer coats), and one black carbonado grain. The data obtained on the mineralogy of the diamonds have demonstrated that they are completely identical to this mineral from kimberlites and lamproites but bear traces of intense dissolution, fragmentation, multiple recrystallization, and graphitization at defects, which are the most widespread in the ballas. One of the crystals was determined to contain inclusions: aggregates of potassic omphacite (0.50 wt % K2O) and corundum. Ilmenite (containing up to 8 wt % MgO), titanaugite, kaersutite (4 wt % TiO2, 0.8 wt % K2O), and churchite (aqueous phosphate) were obtained from the core of the ballas. The titanaugite, kaersutite, and ilmenite were proven to be compositionally analogous to these minerals from picrites occurring near the placer. The carbon isotopic composition δ13C of the cores of the single diamond crystals varies from ?6 to ?11‰. The margins of the grains were proved to be enriched in the light carbon isotope (δ13C from ?19 to ?21‰). The gem-quality transparent diamond crystals are characterized by blue luminescence, and the color of luminescence in the carbonado varies from orange red in the bulk of the aggregate to yellowish green in its core. The aforementioned transformations of diamonds were likely caused by their transportation in pipes of micaceous picrites of the Jurassic meymechite complex. The carbonado are thought to correspond to the final stage of the metastable recrystallization (in pores, within the temperature range of the rutile-anatase transition) of the original isotopically heavy diamonds under the effect of various oxidizers (H2O, CO2, F, and others) and in the presence of catalytically acting REE, Ti, and P. The primary diamond source (kimberlite or lamproite) can be older and more distant from the study area. The complete geological analogy between the study area in Primorie, Kalimantan Island in Indonesia, and West Australia (where no sources of the placers are known) led us to consider the territory of Primorie as promising for exploration for diamondiferous placers.  相似文献   

5.
The authors’ database (which includes data from more than 17500 publications on fluid and melt inclusions in minerals) was used to generalize information on the principal physicochemical parameters of natural mineral-forming fluids (temperature, pressure, density, salinity of aqueous solutions, and the gas composition of the fluids). For 21 minerals, data are reported on the frequency of occurrence of the homogenization temperatures of fluid inclusions in various temperature ranges, which make it possible to reveal temperature ranges most favorable for the crystallization of these minerals. Data on 5260 determinations were used to evaluate the frequency of occurrence of certain temperature and pressure ranges of natural fluids within the temperature intervals of 20–1200°C and 1–12000 bar. Within these intervals, frequencies of occurrence were evaluated for water-dominated and water-poor or water-free fluid inclusions in minerals. The former are predominant at temperatures below 600°C and pressures below 4000 bar, whereas the latter dominate at temperatures of 600–1200°C and pressures of 4000-12000 bar. Illustrative examples are presented for visually discernible magmatic water that exists as an individual high-density phase in melt inclusions in minerals from various rocks sampled worldwide (in the Caucasus, Italy, Slovakia, United States, Uzbekistan, New Zealand, Chile, and others). Attention is drawn to the fact that extensive data testify to fairly high (>1000–1500 bar) pressures during hydrothermal mineral-forming processes. These pressures are much higher not only than the hydrostatic but also the lithostatic pressures of the overlying rocks. Data on more than 18000 determinations are used to evaluate the frequency of occurrence of certain temperature and salinity ranges of mineral-forming fluids within the intervals of 20–1000°C and 0–80 wt % equiv. NaCl and certain temperature and density ranges of these fluids at 20–1000°C and 0.01–1.90 g/cm3. Information is presented on the gas analysis methods most commonly applied to natural fluids in studying fluid inclusions in minerals in 1965–2007. The average composition of the gaseous phase of natural inclusions is calculated based on more than 3000 Raman spectroscopic analyses (the most frequently used method for analyzing individual inclusions).  相似文献   

6.
The staged high-pressure annealing of natural cubic diamonds with numerous melt microinclusions from the Internatsional’naya kimberlite pipe was studied experimentally. The results mainly show that the carbonate phases, the daughter phases in partially crystallized microinclusions in diamonds, may undergo phase transformations under the mantle P–T conditions. Most likely, partial melting and further dissolution of dolomite in the carbonate–silicate melt (homogenization of inclusions) occur in inclusions. The experimental data on the staged high-pressure annealing of diamonds with melt microinclusions allow us to estimate the temperature of their homogenization as 1400–1500°C. Thus, cubic diamonds from the Internatsional’naya pipe could have been formed under quite high temperatures corresponding to the lithosphere/asthenosphere boundary. However, it should be noted that the effect of selective capture of inclusions with partial loss of volatiles in relation to the composition of the crystallization medium is not excluded during the growth. This may increase the temperature of their homogenization significantly between 1400 and 1500°C.  相似文献   

7.
Information from a database, which was compiled and continuously updated by the authors of this paper and now includes information from 19500 publication on fluid and melt inclusions in minerals, is used to summarize results on the physicochemical formation parameters of hydrothermal Au, Ag, Pb, and Zn deposits. The database provides information on fluid inclusions in minerals from 970 Pb-Zn, 220 Au-Ag-Pb-Zn, and 825 Au-Ag deposits in various settings worldwide. Histograms for the homogenization temperatures of fluid inclusion are presented for the most typical minerals of the deposits. In sphalerite, most homogenization temperatures (1327 measurements) of fluid inclusions lie within the range of 50–200°C with a maximum at 100–200°C for this mineral from Pb-Zn deposits and within the range of 100–350°C (802 measurements) with a maximum at 200–300°C for this mineral from Au deposits. Data are presented on fluid pressures at Au (1495 measurements) and Pb-Zn (180 measurements) deposits. The pressure during the preore, ore-forming, and postore stages at these deposits ranged from 4–10 to 6000 bar. The reason for the high pressures during preore stages at the deposits is the relations of the fluids to acid magmatic and metamorphic processes. More than 70% of the fluid pressures values measured at Pb-Zn deposits lie within the range of 1–1500 bar. Au-Ag deposits are characterized by higher fluid pressures of 500–2000 bar (61% of the measurements). The overall ranges of the salinity and temperature of the mineral-forming fluid at Au-Ag (6778 measurements) and Pb-Zn (3395 measurements) deposits are 0.1–80 wt % equiv. NaCl and 20–800°C. Most measurements (～64%) for Au-Ag deposits yield fluid salinity <10 wt % equiv. NaCl and temperatures of 200–400°C (63%). Fluids at Pb-Zn deposits are typically more saline (10–25 wt % equiv. NaCl, 51% measurements) and lower temperature (100–300°C, 74% measurements). Several measurements of the fluid density fall within the range of 0.8–1.2 g/cm3. The average composition of volatile components of the fluids was evaluated by various techniques. The average composition of volatile components of fluid inclusions in minerals is calculated for hydrothermal W, Au, Ag, Sn, and Pb-Zn deposits, metamorphic rocks, and all geological objects. The Au, Ag, Pb, and Zn concentrations in magmatic melts and mineral-forming fluids is evaluated based on analyses of individual inclusions.  相似文献   

8.
There are many melt and fluid inclusions (mainly CO2-rich) in olivine and pyroxene phenocrysts in basalts from the Ross Island area. The melt inclusions can be classified as follows: (1) crystalline melt inclusions (type I), (2) fluid-melt inclusions (type II) and (3) glass inclusions (type III). The daughter minerals in type I include olivine, plagioclase, ilmenite, etc. Fluid-melt inclusions are a new type which represent the immiscibility of magma and fluid at a particular stage of evolution. Three types of fluid-melt inclusions were examined in this study: a) crystal + liquid + gas, b) inclusions coexisting with glass inclusions and fluid inclusions, and c) crystal + daughter mineral (dissolved salt) + gas. Both primary and secondary melt inclusions are recognizable in the samples. The secondary melt inclusions were formed during healing of fractures in the host minerals in the process of magma rise. The homogenization temperatures (both Leitz 1350 stage and quench method were used) of melt inclusions in basalts range from 1190 to 135°C at high pressure (about 7 kbars), indicating that the basalts may have come from the upper mantle. Melt-fluid immiscibility in basaltic magma shows that the CO2-rich fluids may be the main fluid phase in the upper mantle, which are of significance in understanding the evolution of magma and various processes in the deep levels of the earth. The homogenization temperatures of melt and aqueous fluid inclusions in granites and metamorphic rocks in this area vary from 980 to 1100°C and 279 to 350°C, respectively.  相似文献   

9.
Gold deposits in the Taihang Mountains, northern China, mainly consist of quartz sulfide veins in granitoid plutons. This paper describes the geological setting of the gold deposits, and presents the results of microthermometric, Fourier transform infrared spectra, and stable isotope analyses of ore—forming fluids for the purpose of examining the characteristics of these fluids. The ore—forming fluid was of high temperature (up to 380°C) and high salinity (33–41 wt% NaCl equiv.), represented by type I inclusions (with daughter minerals). This fluid evolved to low salinity at low temperatures recorded in type II (liquid-rich) and III inclusions (vapor—rich). Primary type II inclusions coexist with type III inclusions in quartz. Type III inclusions have almost the same homogenization temperatures as type II inclusions. This probably reflects boiling. The secondary fluid inclusions homogenized at lower temperatures, and have lower salinities than primary inclusions. Based on microthermometric data, we propose that the high—temperature fluid that separated from residual magma corresponded to the ore—forming fluid represented by type I inclusions. This fluid mixed with meteoric water in the upper part of the granitic pluton and was diluted. The diluted fluid boiled, probably due to abrupt pressure decrease, and formed liquid—rich type II inclusions and vapor—rich type III inclusions. The deposition of sulfide minerals and gold probably occurred during boiling.  相似文献   

10.
The first data of chromatography—mass spectrometry analysis of volatiles from crystals of synthetic diamonds grown in a Fe—Ni—C system at 1350–1400°С and 5.5–6.0 GPa are presented. The composition of the fluid in equilibrium with the metal-carbon melt is determined, and a comparative estimation for the compounds of different hydrocarbons and their derivatives is made. It is shown that a significant role in these processes is played by high-molecular-weight hydrocarbons; and the total share of hydrocarbons and their derivatives in the fluid compounds can exceed 86%.  相似文献   

11.
Kuh-I-Mond field in the Zagros foreland basin is a conventional heavy oil resource and is composed of fractured carbonates whose fractures were filled by calcite, dolomite, and anhydrite cements. Oil inclusions occurred within the fracture-fill cements indicate that fractures were open and played an active role during oil migration and charge. The highest measured values for secondary porosities belong to fractures in Asmari Formation, which is characterized by significant amounts of vug- and fracture-filling cements. Fractures facilitated fluid circulation and subsequently dissolution of allochems and high Mg carbonates. In contrast, fine-grained carbonate facies were less cemented, and thus, porosity enhancement by cement dissolution was insignificant. Temperature profiles of oil inclusions in the dolomite, calcite, and anhydrite minerals characterized by distinct variations in the homogenization temperatures (Th) that are divided into two ranges below 50°C in anhydrites and from 45°C to 125°C in dolomites and calcites. The lower Th ranges for anhydrite suggests that it may have formed at shallower burial depths during early to middle diagenesis. The oil inclusions display trend for increasing temperature downward which conform to Formation geothermal gradient. In other word, the decreasing trend of Th temperatures upward within Asmari Formation that can be observed in Th versus depth plot is consistent with the uplift events at Late Miocene time and later that caused removal of about 1,300 m of the crest of the Kuh-I-Mond anticline. Vitrinite reflectance data from source rock intervals in the field area do not support vertical migration of locally generated hydrocarbons into the Kuh-I-Mond accumulation, and long-distance lateral oil migration and charge from a source kitchen to the southwest is proposed. Vitrinite reflectance data from this dolomite and limestone reservoir suggest low maturation levels corresponding to paleotemperatures less than 50°C. The observed maturation level (<0.5% Ro) does not exceed values for simple burial maturation based on the estimated burial history. Also, homogenization temperatures from fluid inclusion populations in calcite and dolomites show expected good correlation with reflectance-derived temperatures. The Th data represent pore fluids became warmer and more saline during burial. As aqueous fluid inclusions in calcite veins were homogenized between 22°C and 90°C with a decrease in salinity from 22 to 18 eq.?wt.% NaCl. The Th values suggest a change in water composition and that dolomite and calcite cements might have precipitated from petroleum-derived fluids. The hydrocarbon fluid inclusions microthermometry data suggest that the reservoir was being filled by heavy black oils in reservoir during Cenozoic. Aqueous fluid inclusions hosted by calcite equant sparry/fossil cavity fills suggest low cementation temperatures (<45°C) and high salinities (19 eq.?wt.% NaCl), while those in dolostones are characterized by highly variable homogenization temperature (52°C to 125°C) and salinities (6.5 to 20 eq.?wt.% NaCl).  相似文献   

12.
Mo-Bi mineralization occurs in subvertical and subhorizontal quartz-muscovite-± K-feldspar veins surrounded by early albitic and later K-feldspathic alteration halos in monzogranite of the Archean Preissac pluton, Abitibi region, Québec, Canada. Molybdenite is intergrown with muscovite in the veins or associated with K-feldspar in the alteration halos. Mineralized veins contain five main types of fluid inclusions: aqueous liquid and liquid-vapor inclusions, aqueous carbonic liquid-liquid-vapor inclusions, carbonic liquid and vapor inclusions, halite-bearing aqueous liquid and liquid-vapor inclusions, trapped mineral-bearing aqueous liquid and liquid-vapor inclusions. The carbonic solid in frozen carbonic and aqueous-carbonic inclusions melts in most cases at −56.7 ± 0.1 °C indicating that the carbonic fluid consists largely of CO2. All aqueous inclusion types and the aqueous phase in carbonic inclusions have low initial melting temperatures (≥70 °C), requiring the presence of salts other than NaCl. Leachate analyses show that the bulk fluid contains variable proportions of Na, K, Ca, Cl, and traces of Mg and Li. The following solids were identified in the fluid inclusions by SEM-EDS analysis: halite, calcite, muscovite, millerite (NiS), barite and antarcticite (CaCl2 · 6H2O). All are interpreted to be trapped phases except halite which is a daughter mineral, and antarcticite which formed during sample preparation (freezing). Aqueous inclusions homogenize to liquid at temperatures between 75 °C and 400 °C; the mode is 375 °C. Aqueous-carbonic inclusions homogenize to liquid or vapor between 210 °C and 400 °C. Halite-bearing aqueous inclusions homogenize by halite dissolution at approximately 170 °C. Aqueous inclusions containing trapped solids exhibit liquid-vapor homogenization at temperatures similar to those of halite-bearing aqueous inclusions. Temperatures of vein formation, based on oxygen isotopic fractionation between quartz and muscovite, range from 342 °C to 584 °C. The corresponding oxygen isotope composition of the aqueous fluid in equilibrium with these minerals ranges from 1.2 to 5.5 per mil with a mean of 3.9 per mil, suggesting that the liquid had a significant meteoric component. Isochores for aqueous fluid inclusions intersect the modal isotopic isotherm of 425 °C at pressures between 590 and 1900 bar. A model is proposed in which molybdenite was deposited owing to decreasing temperature and/or pressure from CO2-bearing, moderate to high salinity fluids of mixed magmatic-meteoric origin that were in equilibrium with K-feldspar and muscovite. These fluids resulted from the degassing of a monzogranitic magma and evolved through interaction with volcanic (komatiitic) and sedimentary country rocks. Received: 6 February 1997 / Accepted: 28 January 1998  相似文献   

13.
The Degdekan and Gol’tsovsky gold-quartz deposits are located in the southeastern Yana-Kolyma gold belt. The orebodies occur as quartz veins hosted in metaterrigenous rocks and cut by postmineral basic-intermediate dikes. It was established that metamorphism of sulfides and gangue quartz was restricted to a few centimeters off the dike contact. According to sulfide geothermometers, the metamorphic temperatures close to the contact of dikes attained 700°C at the Degdekan deposit and were no higher than 491°C at the Gol’tsovsky deposit. The formation of the forbidden assemblage of quartz and loellingite and its fine-grained texture indicate that the thermal effect on the Degdekan ore was short-term. The prolonged heating of the ore at the Gol’tsovsky deposit gave rise to the aggradation recrystallization of quartz and the formation of equilibrium sulfide aggregates that show only insignificant differences in composition from the primary phases. The average homogenization temperature of primary and pseudosecondary fluid inclusions is 206 ± 40°C in the unmetamorphosed veins and 257 ± 33°C in the metamorphosed veins. The salinity of fluids in the primary and pseudosecondary inclusions in quartz veins of both types varies from 0.5 to 14.0 wt % NaCl equiv. The melting temperature of liquid CO2 in the carbon dioxide inclusions, ranging from ?57.0 to ?60.8°C, suggests an admixture of CH4 and/or N2. The unmetamorphosed quartz veins were formed at a fluid pressure varying from 0.7 to 1.3 kbar, while quartz veins at the contact with dikes crystallized at a pressure of 0.8–1.5 kbar. The results of gas chromatography showed the presence of CO2 and H2O, as well as N2 and CH4. The average bulk of volatiles contained in the fluid inclusions in quartz from the metamorphosed veins is 1.5–2 times lower than in the unmetamorphosed veins; this proportion is consistent with the occurrence of decrepitated gas inclusions in the heated quartz.  相似文献   

14.
Abundant fluid-melt inclusions are found in the aegirine-augite-barite pegmatite and carbonatite veins in the Mianning REE deposit,Sichuan,They were trapped in early stage fluorite and quartz from a salt-melt system at temperatures higher than 5000℃,Meanwhile,fluid inclusions are also present in alrge amounts in bastnaesite.Homogenized between 150 and 270℃,these inclusions are thought to be representative of the physico-chemical conditions of REE mineralization.These results show that the Mianning REE deposit is of typical hydrothermal origin developed from a salt-melt system.  相似文献   

15.
Fluid inclusion studies in combination with hydrogen, oxygen and sulphur isotope data provide novel insights into the genesis of giant amethyst-bearing geodes in Early Cretaceous Paraná continental flood basalts at Amestita do Sul, Brazil. Monophase liquid inclusions in colourless quartz, amethyst, calcite, barite and gypsum were analysed by microthermometry after stimulating bubble nucleation using single femtosecond laser pulses. The salinity of the fluid inclusions was determined from ice-melting temperatures and a combination of prograde and retrograde homogenisation temperatures via the density maximum of the aqueous solutions. Four mineralisation stages are distinguished. In stage I, celadonite, chalcedony and pyrite formed under reducing conditions in a thermally stable environment. Low δ34SV-CDT values of pyrite (?25 to ?32?‰) suggest biogenic sulphate reduction by organotrophic bacteria. During the subsequent stages II (amethyst, goethite and anhydrite), III (early subhedral calcite) and IV (barite, late subhedral calcite and gypsum), the oxidation state of the fluid changed towards more oxidising conditions and microbial sulphate reduction ceased. Three distinct modes of fluid salinities around 5.3, 3.4 and 0.3 wt% NaCl-equivalent characterise the mineralisation stages II, III and IV, respectively. The salinity of the stage I fluid is unknown due to lack of fluid inclusions. Variation in homogenisation temperatures and in δ18O values of amethyst show evidence of repeated pulses of ascending hydrothermal fluids of up to 80–90 °C infiltrating a basaltic host rock of less than 45 °C. Colourless quartz and amethyst formed at temperatures between 40 and 80 °C, while the different calcite generations and late gypsum precipitated at temperatures below 45 °C. Calculated oxygen isotope composition of the amethyst-precipitating fluid in combination with δD values of amethyst-hosted fluid inclusions (?59 to ?51?‰) show a significant 18O-shift from the meteoric water line. This 18O-shift, high salinities of the fluid inclusions with chloride-sulphate composition, and high δ34S values of anhydrite and barite (7.5 to 9.9?‰) suggest that sedimentary brines from deeper parts of the Guaraní aquifer system must have been responsible for the amethyst mineralisation.  相似文献   

16.
The porphyry Cu deposits at Waisoi in Namosi district, Viti Levu are separated into two deposits: the Waisoi East deposit and the Waisoi West deposit. In the Waisoi East deposit, quartz porphyry is exposed and in the Waisoi West deposit, diorite porphyry is sporadically exposed in addition to a small body of quartz porphyry. The mineralization in the Waisoi East deposit is characterized by the bornite–chalcopyrite–pyrite assemblage associated with traces of molybdenite and native gold. Polyphase fluid inclusions in stockwork quartz veinlets show homogenization temperatures ranging from 210 to >500°C. The high‐grade Cu mineralization in the Waisoi West deposit is characterized by the bornite–chalcopyrite–pyrite assemblage accompanied with sheeted and stockwork quartz veinlets. Polyphase fluid inclusions occasionally containing hematite flakes in quartz veinlets in the center of the Waisoi West deposit homogenize at temperatures ranging from 450°C to >500°C. However, fluid inclusions in stockwork quartz veinlets in the periphery, homogenize at lower temperatures around 210°C. Both in the Waisoi East and Waisoi West deposits, primary bornite–chalcopyrite–pyrite assemblage in the high Cu‐grade zone was deposited at the upper stability limit of chalcopyrite with respect to sulfur fugacity. Thus, the principal Cu mineralization at the Waisoi deposits occurred at a relatively high sulfur fugacity, that is, in a high‐sulfidation environment.  相似文献   

17.
The ultrahigh-temperature (UHT) metamorphism of the Napier Complex is characterized by the presence of dry mineral assemblages, the stability of which requires anhydrous conditions. Typically, the presence of the index mineral orthopyroxene in more than one lithology indicates that H2O activities were substantially low. In this study, we investigate a suite of UHT rocks comprising quartzo-feldspathic garnet gneiss, sapphirine granulite, garnet-orthopyroxene gneiss, and magnetite-quartz gneiss from Tonagh Island. High Al contents in orthopyroxene from sapphirine granulite, the presence of an equilibrium sapphirine-quartz assemblage, mesoperthite in quartzo-feldspathic garnet gneiss, and an inverted pigeonite-augite assemblage in magnetite-quartz gneiss indicate that the peak temperature conditions were higher than 1,000 °C. Petrology, mineral phase equilibria, and pressure-temperature computations presented in this study indicate that the Tonagh Island granulites experienced maximum P-T conditions of up to 9 kbar and 1,100 °C, which are comparable with previous P-T estimates for Tonagh and East Tonagh Islands. The textures and mineral reactions preserved by these UHT rocks are consistent with an isobaric cooling (IBC) history probably following an counterclockwise P-T path. We document the occurrence of very high-density CO2-rich fluid inclusions in the UHT rocks from Tonagh Island and characterize their nature, composition, and density from systematic petrographic and microthermometric studies. Our study shows the common presence of carbonic fluid inclusions entrapped within sapphirine, quartz, garnet and orthopyroxene. Analysed fluid inclusions in sapphirine, and some in garnet and quartz, were trapped during mineral growth at UHT conditions as 'primary' inclusions. The melting temperatures of fluids in most cases lie in the range of -56.3 to -57.2 °C, close to the triple point for pure CO2 (-56.6 °C). The only exceptions are fluid inclusions in magnetite-quartz gneiss, which show slight depression in their melting temperatures (-56.7 to -57.8 °C) suggesting traces of additional fluid species such as N2 in the dominantly CO2-rich fluid. Homogenization of pure CO2 inclusions in the quartzo-feldspathic garnet gneiss, sapphirine granulite, and garnet-orthopyroxene gneiss occurs into the liquid phase at temperatures in the range of -34.9 to +4.2 °C. This translates into very high CO2 densities in the range of 0.95-1.07 g/cm3. In the garnet-orthopyroxene gneiss, the composition and density of inclusions in the different minerals show systematic variation, with highest homogenization temperatures (lowest density) yielded by inclusions in garnet, as against inclusions with lowest homogenization (high density) in quartz. This could be a reflection of continued recrystallization of quartz with entrapment of late fluids along the IBC path. Very high-density CO2 inclusions in sapphirine associated with quartz in the Tonagh Island rocks provide potential evidence for the involvement of CO2-rich fluids during extreme crustal temperatures associated with UHT metamorphism. The estimated CO2 isochores for sapphirine granulite intersect the counterclockwise P-T trajectory of Tonagh Island rocks at around 6-9 kbar at 1,100 °C, which corresponds to the peak metamorphic conditions of this terrane derived from mineral phase equilibria, and the stability field of sapphirine + quartz. Therefore, we infer that CO2 was the dominant fluid species present during the peak metamorphism in Tonagh Island, and interpret that the fluid inclusions preserve traces of the synmetamorphic fluid from the UHT event. The stability of anhydrous minerals, such as orthopyroxene, in the study area might have been achieved by the lowering of H2O activity through the influx of CO2 at peak metamorphic conditions (>1,100 °C). Our microthermometric data support a counterclockwise P-T path for the Napier Complex.  相似文献   

18.
Diamonds from the Kankan area in Guinea formed over a large depth profile beginning within the cratonic mantle lithosphere and extending through the asthenosphere and transition zone into the lower mantle. The carbon isotopic composition, the concentration of nitrogen impurities and the nitrogen aggregation level of diamonds representing this entire depth range have been determined. Peridotitic and eclogitic diamonds of lithospheric origin from Kankan have carbon isotopic compositions ('13C: peridotitic -5.4 to -2.2‰; eclogitic -19.7 to -0.7‰) and nitrogen characteristics (N: peridotitic 17-648 atomic ppm; eclogitic 0-1,313 atomic ppm; aggregation from IaA to IaB) which are generally typical for diamonds of these two suites worldwide. Geothermobarometry of peridotitic and eclogitic inclusion parageneses (worldwide sources) indicates that both suites formed under very similar conditions within the cratonic lithosphere, which is not consistent with a derivation of diamonds with light carbon isotopic composition from subducted organic matter within subducting oceanic slabs. Diamonds containing majorite garnet inclusions fall to the isotopically heavy side ('13C: -3.1‰ to +0.9‰) of the worldwide diamond population. Nitrogen contents are low (0-126 atomic ppm) and one of the two nitrogen-bearing diamonds shows such a low level of nitrogen aggregation (30% B-centre) that it cannot have been exposed to ambient temperatures of the transition zone (̿,400 °C) for more than 0.2 Ma. This suggests rapid upward transport and formation of some Kankan diamonds pene-contemporaneous to Cretaceous kimberlite activity. Similar to these diamonds from the asthenosphere and the transition zone, lower mantle diamonds show a small shift towards isotopic heavy compositions (-6.6 to -0.5‰, mode at -3.5‰). As already observed for other mines, the nitrogen contents of lower mantle diamonds were below detection (using FTIRS). The mutual shift of sublithospheric diamonds towards isotopic heavier compositions suggests a common carbon source, which may have inherited an isotopic heavy composition from a component consisting of subducted carbonates.  相似文献   

19.
Abstract. Evolution of hydrothermal system from initial porphyry Cu mineralization to overlapping epithermal system at the Dizon porphyry Cu‐Au deposit in western central Luzon, Zambales, Philippines, is documented in terms of mineral paragen‐esis, fluid inclusion petrography and microthermometry, and sulfur isotope systematics. The paragenetic stages throughout the deposit are summarized as follows; 1) stockwork amethystic quartz veinlets associated with chalcopyrite, bornite, magnetite and Au enveloped by chlorite alteration overprinting biotite alteration, 2) stockwork quartz veinlets with chalcopyrite and pyrite associated with Au and chalcopyrite and pyrite stringers in sericite alteration, 3) stringer quartz veinlets associated with molybdenite in sericite alteration, and 4) WNW‐trending quartz veins associated with sphalerite and galena at deeper part, while enargite and stibnite at shallower levels associated with advanced argillic alteration. Chalcopyrite and bornite associated with magnetite in quartz veinlet stockwork (stage 1) have precipitated initially as intermediate solid solution (iss) and bornite solid solution (bnss), respectively. Fluid inclusions in the stockwork veinlet quartz consist of gas‐rich inclusions and polyphase inclusions. Halite in polyphase inclusions dissolves at temperatures ranging from 360d?C to >500d?C but liquid (brine) and gas (vapor) do not homogenize at <500d?C. The maximum pressure and minimum temperature during the deposition of iss and bnss with stockwork quartz veinlets are estimated to be 460 bars and 500d?C. Fluid inclusions in veinlet stockwork quartz enveloped in sericite alteration (stage 2) consist mainly of gas‐rich inclusions and polyphase inclusions. In addition to the possible presence of saturated NaCl crystals at the time of entrapment of fluid inclusions that exhibit the liquid‐vapor homogenization temperatures lower than the halite dissolution temperatures in some samples, wide range of temperatures of halite dissolution and liquid‐vapor homogenization of polyphase inclusions from 230d?C to >500d?C and from 270d?C to >500d?C, respectively, suggests heterogeneous entrapment of gaseous vapor and hypersaline brine. The minimum pressure and temperature are estimated to be about 25 bars and 245d?C. Fluid inclusions in veinlet quartz associated with molybdenite (stage 3) are dominated by gas‐rich inclusions accompanied with minor liquid‐rich inclusions that homogenize at temperatures between 350d?C and 490d?C. Fluid inclusions in vuggy veinlet quartz associated with stibnite (stage 4) consist mainly of gas‐rich inclusions with subordinate polyphase inclusions that do not homogenize below 500d?C. Fluid inclusions in veinlet quartz associated with galena and sphalerite (stage 4) are composed of liquid‐rich two‐phase inclusions, and they homogenize into liquid phase at temperatures ranging widely from 190d?C to 300d?C (suggesting boiling) and the salinity ranges from 1.0 wt% to 3.4 wt% NaCl equivalent. A pressure of about 15 bars is estimated for the dilute aqueous solution of 190d?C from which veinlet quartz associated with galena and sphalerite precipitated. In addition to a change in temperature‐pressure regime from lithostatic pressure during the deposition of iss and bnss with stockwork quartz veinlets to hydrostatic pressure during fracture‐controlled quartz veinlet associated with galena and sphalerite, a decrease in pressure is supposed to have occurred due to unroofing or removal of the overlying piles during the temperature decrease in the evolution of hydrothermal system. The majority of the sulfur isotopic composition of sulfides ranges from ±0 % to +5 %. Sulfur originated from an iso‐topically uniform and homogeneous source, and the mineralization occurred in a single hydrothermal system.  相似文献   

20.
The quartz grains from the sandstone of Jaisalmer, Pariwar and Goru Formations of the Jaisalmer basin, Rajasthan, India, exhibits a variety of primary and secondary fluid inclusions. Most of them are hydrocarbon bearing fluid inclusions. Laser Raman studies indicate that the primary fluid inclusions were mostly having aliphatic hydrocarbons with lower degree of maturity, while the secondary fluid inclusions were generally with aliphatic as well as aromatic hydrocarbons with higher degree of maturity. This inference was consistent with their fluorescence characteristics. The homogenization temperatures of primary monophase CH4 rich fluid inclusions varied from ?80°C to ?100°C, whereas the primary biphase fluid inclusions (CH4-CO2) homogenized between +80°C and +150°C. The secondary petroleum rich monophase fluid inclusions were having homogenization temperature between ?80°C to ?90°C, whereas the secondary biphase fluid inclusions homogenized between +130°C and +180°C. Most of the secondary biphase fluid inclusions were having the mixtures of H2O-CO2-NaCl, and were identified on the basis clathrate formation and they got homogenized between +140°C and + 250 °C. The three past events of migration of petroleum inferred in the host rock which were marked by the presence of characteristic secondary fluid inclusions. They were identified on the basis of cross-cutting relationships of different trails of fluid inclusions in the quartz. The cement generation in the basin might have been occurred in two stages as per the fluid inclusion petrography.  相似文献   

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