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1.
Calculation of muscovite-paragonite-alkali feldspar phase relations   总被引：1，自引：0，他引：1  
Experimental data on K-Na exchange between NaCl-KCl-H2O fluids and alkali feldspars or white micas, and end-member dehydration reactions of white mica (± quartz to alkali feldspar plus corundum (or Al2SiO5) and H2O have been used to evaluate K-Na exchange potentials between coexisting white mica and alkali feldspar. Calculations using these exchange potentials and Margules parameters for excess molar Gibbs energies of alkali feld-spars and white micas have permitted the construction of a projected binary phase diagram for the white mica dehydration. Extrapolation to higher temperatures and pressures gives a topology wholly consistent with field evidence. The subsolidus univariant curves intersect H2O-saturated minimum-melting curves. At pressures greater than about 6 kbar the common assemblage Ms+Or+Ab+Q could undergo H2O-saturated minimum-melting at lower temperatures than the disappearance of paragonite or the kyanite-sillimanite isograd in more aluminous rocks. The apparent restriction of anatexis to rocks above the second sillimanite isograd may imply that activity of H2O is usually less than unity in high-grade regional metamorphism.  相似文献   

2.
为开展松辽盆地深部长期观测、流体实验和探索白垩纪火山事件,利用松科二井东孔丰富、齐全的测井资料,对营城组火山岩岩性进行评价。通过测井响应特征分析发现,松科二井东孔营城组凝灰岩具有最强的放射性和导电性,高孔隙度的集块熔岩密度为低值,流纹岩表现出高密度和低导电性。利用测井交会图和成像识别模式,识别出松科二井东孔营城组火山岩以流纹岩、凝灰熔岩和集块熔岩为主,少量的凝灰岩。结合凝灰岩处测井曲线变化特点,证明了火山喷发间断的存在。流纹岩具有高碱、高Si、低Fe和低黏土矿物特征。T_2谱分析认为流纹岩有利于后期深部长期观测和流体实验的开展。研究成果对松科二井东孔后续火石岭组火成岩及整个松辽盆地火山岩研究具有一定的参考价值。  相似文献   

3.
The carbonatite at Magnet Cove, Arkansas, USA contains a great variety and abundance of magmatic and hydrothermal inclusions that provide an informative, though fragmentary, record of the original carbonatite melt and of late hydrothermal solutions which permeated the complex in postmagmatic time. These inclusions were studied by optical and scanning electron microscopy. Primary magmatic inclusions in monticellite indicate that the original carbonatite melt contained approximately 49.7 wt% CaO, 16.7% CO2, 15.7% SiO2, 11.4% H2O, 4.4% FeO+Fe2O3, 1.1% P2O5 and 1.0% MgO. The melt was richer in SiO2 and iron oxides than the carbonatite as now exposed; this is attributed to crystal settling and relative enrichment of calcite at shallower levels. The density of the carbonatite melt as revealed by the magmatic inclusions was approximately 2.2–2.3 g/cc. Such a light melt should separate rapidly from any denser parent material and could be driven forcibly into overlying crustal rocks by buoyant forces alone. Fluid inclusions in apatite suggest that a separate (immiscible) phase composed of supercritical CO2 fluid of low density coexisted with the carbonatite magma, but the inclusion record in this mineral is inconclusive with respect to the nature of any other coexisting fluids. Maximum total pressure during CO2 entrapment was about 450 bars, suggesting depths of 1.5 km or less for apatite crystallization and supporting earlier proposals of a shallow, subvolcanic setting for the complex. Numerous secondary inclusions in the Magnet Cove calcite contain an intriguing variety of daughter minerals including some 19 alkali, alkaline earth and rare earth carbonates, sulfates and chlorides few of which are known as macroscopic phases in the complex. The exotic fluids from which the daughter minerals formed are inferred to have cooled and diluted through time by progressive mixing with local groundwaters. These fluids may be responsible for certain late veins and elemental enrichments associated with the complex.  相似文献   

4.
The paper describes the first finding of quintinite [Mg4Al2(OH)12][(CO3)(H2O)3] at the Mariinsky deposit in the Central Urals, Russia. The mineral occurs as white tabular crystals in cavities within altered gabbro in association with prehnite, calcite, and a chlorite-group mineral. Quintinite is the probable result of late hydrothermal alteration of primary mafic and ultramafic rocks hosting emerald-bearing glimmerite. According to electron microprobe data, the Mg: Al ratio is ~2: 1. IR spectroscopy has revealed hydroxyl and carbonate groups and H2O molecules in the mineral. According to single crystal XRD data, quintinite is monoclinic, space group C2/m, a =5.233(1), b = 9.051(2), c = 7.711(2) Å, β = 103.09(3)°, V = 355.7(2) Å3. Based on structure refinement, the polytype of quintinite should be denoted as 1M. This is the third approved occurrence of quintinite-1M in the world after the Kovdor complex and Bazhenovsky chrysotile–asbestos deposit.  相似文献   

5.
The Söndrum stone quarry (Halmstad, SW Sweden) exposes a transition from migmatized granitic gneissic country rock into a foliated clinopyroxene‐free granitic gneiss, and then a central pegmatoid dyke dominated by clinopyroxene megacrysts. This transition zone represents a fracture‐controlled, fluid‐alteration zone that developed under conditions of 650–700 °C and 790 MPa. Mineral chemical trends in F, Cl, Fe, Ti, Mn and Y are interpreted as documenting a fluid infiltration event associated with the formation of the pegmatoid dyke. Fluid inclusions from the pegmatoid dyke are CO2 dominant, whereas in the surrounding country rock they are dominated by H2O‐NaCl‐CaCl2. Fluid inclusions from the intermediate foliated clinopyroxene‐free granitic gneiss are a mixture of the two types. The pegmatoid dyke appears to have originated from a high Ca activity, Fe‐Mg enriched, fluid‐rich granitic melt with a CO2 component, which was emplaced along a tectonic fracture in a regionally migmatized granitic gneiss in the lower crust. This was accompanied by limited partial melting of the surrounding granitic gneiss. The Ca activity of the melt was high enough to allow for the formation of clinopyroxene megacrysts as opposed to orthopyroxene. H2O‐enriched fluids expelled from the crystallizing pegmatoid dyke, which retained the majority of the CO2 helping to stabilize the clinopyroxene. The expelled fluids coarsened and chemically affected the surrounding country rock resulting in trends in the mineral and fluid inclusion chemistry seen today in the foliated and regional granitic gneiss.  相似文献   

6.
Strata-bound antimony, mercury, tungsten and massive sulfide mineralization occurs within a metamorphosed Paleozoic volcanosedimentary sequence in the Kreuzeck Mountains, Austria. Amphibolites are a significant constituent of that sequence; on the basis of stable trace element data, they can be classified as metamorphic equivalents of recent olivine tholeiites. In the ore environment of strata-bound mineralization, intensive alteration associated with submarine hydrothermal activity has affected the wall rocks. This includes depletion in SiO2, a change in the oxidation stage of iron and pronounced enrichment in Na, Sr, Ba and CO2. Microprobe analyses reveal lower MgO content in chlorites and higher Na2O content in feldspars in rocks from the ore environment. Hydrothermal halos are thus documented by changes in mineral and whole-rock compositions and represent guides to exploration.  相似文献   

7.
The petrography, mineral chemistry and petrogenesis of a sample from the Weissenstein eclogite, Bavaria, Germany, has been investigated. The total mineral assemblage comprises garnet, clinopyroxeneI+II, quartz, amphiboleI+II, rutile, phengite, epidote/allanite, plagioclase, biotite, apatite, pumpellyite, titanite (sphene), zircon, alkali feldspar and calcite. Textural observations combined with geothermobarometry (Fe/Mg distribution between clinopyroxene/garnet and phengite/garnet; jadeite-content of omphacite, Si-content of phengite, and An-content of plagioclase) provide indications of two different stages in the metamorphic evolution of the rock. The main phengitequartz-eclogite mineral equilibration occurred at minimum P=13–17kbar, minimum T=620±50° C; the retrograde symplectite stage (clinopyroxeneII, amphiboleII, biotite, plagioclase) occurred at P total between 12 and 8.5 kbar. Reactions of the symplectite stage are:
  1. phengite (core) + Na2Oaq + CaOaq=phengite (rim) + biotite + plagioclase + K2Oaq + H2O
  2. phengite (core) + clinopyroxeneI + Na2Oaq=phengite (rim + biotite + plagioclase + amphiboleII + SiO2 + K2Oaq + CaOaq + H2O
  3. clinopyroxeneI + SiO2 + K2Oaq + H2O=clinopyroxeneII + plagioclase+amphiboleII + Na2Oaq + CaOaq
The phengite decomposition produces H2O, whereas the clinopyroxene decomposition consumes H2O. The estimated P-T-conditions for the Weissenstein eclogite are in the same order of magnitude as those for other eclogite bodies from the Alps and Caledonides believed to be related to subduction processes.  相似文献   

8.
The Dzhusinskoe pyrite–polymetallic deposit is characterized by an abundant concentration of dykes of basic and intermediate rocks. Thermal metamorphism of ore-host rocks and the recrystallization of ore minerals are associated with the intrusion of post-ore dykes. A regular increase in the homogenization temperature from 156° at a distance from a dyke to 287–305°C in the contact zone was established. Highly saline (6.4–15.7 wt % NaCl eq.) CO2–H2O–NaCl fluids under high pressure (up to 1500 bar) can be associated with the processes of contact and regional metamorphism.  相似文献   

9.
Amphibolite facies metamorphic grade gives way southward to the granulite grade in southern Karnataka, as acid gneisses develop charnockite patches and streaks and basic enclaves develop pyroxenes. Petrologic investigations in the transitional zone south of Mysore have established the following points:
  1. The transition is prograde. Amphibole-bearing gneisses intimately associated with charnockite at Kabbal and several similar localities are not retrogressive after charnockite, as proved by patchy obliteration of their foliation by transgressive, very coarse-grained charnockite, high fluorine content of biotite and amphibole in gneisses, and high large-ion lithophile element contents in gneisses and charnockites. These features are in contrast to very low fluorine in retrogressive amphiboles and biotites, very low large-ion lithophile element contents, and zonal bleaching of charnockite, in clearly retrogressive areas, as at Bhavani Sagar, Tamil Nadu.
  2. Metamorphic temperatures in the transitional areas were 700°–800° C, pressures were 5–7 kbar, and H2O pressures were 0.1–0.3 times total pressures, based on thermodynamic calculations using mineral analyses. Dense CO2-rich fluid inclusions in the Kabbal rocks confirm the low H2O pressures at the first appearance of orthopyroxene. Farther to the south, in the Nilgiri Hills and adjacent granulite massif areas, peak metamorphic temperatures were 800°–900° C, pressures were 7–9 kbar, and water pressures were very low, so that primary biotites and amphiboles (those with high F contents) are rare.
  3. The incipient granulite-grade metamorphism of the transitional areas was introduced by a wave of anatexis and K-metasomatism. This process was arrested by drying out under heavy CO2 influx. Charnockites so formed are hybrids of anatectic granite and metabasite, of metabasite and immediately adjacent gneiss, or are virtually isochemical with pre-existing gneiss despite gross recrystallization to granulite mineralogy. These features show that partial melting and metasomatism are attendant, rather than causative, in charnockite development. Copious CO2 from a deep-crustal or mantle source pushed ahead of it a wave of more aqueous solutions which promoted anatexis. Granulite metamorphism of both neosome and paleosome followed. The process is very similar to that deduced for the Madras granulites by Weaver (1980). The massif charnockites, for the most part extremely depleted in lithophile minor elements, show many evidences of having gone through the same process.
A major problem remaining to be solved is the origin of the large amount of CO2 needed to charnockitize significant portions of the crust. The most important possibilities include CO2 from carbonate minerals in a mantle “hot spot” or diapir, from emanations from a crystallizing basaltic underplate, or from shelf sediments trapped at the continent-continent interface in continental overthrusting. Ancient granulite massifs may be such suture zones of continental convergence.  相似文献   

10.
Phase relations of pumpellyite, epidote, lawsonite, CaCO3, paragonite, actinolite, crossite and iron oxide are analysed on an Al-Ca-Fe3+ diagram in which all minerals are projected from quartz, albite or Jadeite, chlorite and fluid. Fe2+ and Mg are treated as a single component because variation in Fe2+/Mg has little effect on the stability of phases on the diagram. Comparison of assemblages in the Franciscan, Shuksan, Sanbagawa, New Caledonia, Southern Italian, and Otago metamorphic terranes reveals several reactions, useful for construction of a petrogenetic grid:
  1. lawsonite+crossite + paragonite = epidote+chlorite + albite + quartz + H2O
  2. lawsonite + crossite = pumpellyite + epidote + chlorite + albite+ quartz + H2O
  3. crossite + pumpellyite + quartz = epidote + actinolite + albite + chlorite + H2O
  4. crossite + epidote + quartz = actinolite + hematite + albite + chlorite + H2O
  5. calcite + epidote + chlorite + quartz = pumpellyite + actinolite + H2O + CO2
  6. pumpellyite + chlorite + quartz = epidote + actinolite + H2O
  相似文献   

11.
Liquidus experimental studies on kimberlite, lamproite and lamprophyre compositions are reviewed with respect to the information they carry on the mantle origin of these rock types. This information is coupled with melting experiments on peridotite in the presence of H2O and mixed H2O+CO2 volatile species. The origin of most lamproites is explained by the melting of mica-harzburgite assemblages at depths ranging from 40km for leucite lamproites to more than 150km for olivine lamproites. Clinopyroxene-rich, silica-poor lamproites remain enigmatic, but are possibly derived by the melting of a mica-bearing ultramafic source richer in clinopyroxene and under more oxidized, CO2-bearing conditions. There are insufficient experimental studies on kimberlite to reasonably constrain their origin, and what remain are only general indications of the compositions of partial melts of mantle under volatile-bearing conditions. Melt compositions are not sufficiently well known to prevent very conceptual use of melt ‘names’ such as ‘kimberlitic’ or ‘carbonatitic’, and melts similar to alkaline and ultramafic lamprophyre may be hidden under this shroud. Clearer definition of the origins of alkaline melt compositions such as kimberlites and various lamprophyre types badly needs more exact bracketing of melt compositions of a variety of possible mantle mineral assemblages. The recently-developed sandwich reversal technique is ideally suited to study small degrees of partial melting, and could usefully be applied to lherzolitic and non-lherzolitic materials with hydrous and/or carbonate minerals.  相似文献   

12.
Melt inclusions in olivine Fo83–72 from tephras of 1867, 1971 and 1992 eruptions of Cerro Negro volcano represent a series of basaltic to andesitic melts of narrow range of MgO (5.6–8 wt %) formed by ~46 wt % fractional crystallization of olivine (~6 wt %), plagioclase (~27 wt %), pyroxene (~13 wt %) and magnetite (<1 wt %) from primitive basaltic melt (average SiO2 = 49 wt %, MgO = 7.6 wt %, H2O = 6 wt %) as it ascended to the surface from the depth of about 14 km. The crystallization occurred at increasing liquidus temperature from 1,050 to 1,090 °C in the pressure range from 400 to 50 MPa and was induced by release of mixed H2O–CO2 fluid from the melt at decreasing pressure. Matrix glass compositions fall at the high-Si end of the melt inclusion trend and represent the final stage of melt crystallization during and after eruption. The bulk compositions of erupted Cerro Negro magmas (tephras and lavas) range from high- to low-MgO (3–10 wt %) basalts, which form a compositional array crossing the trend of melt inclusions so that virtually no rock from Cerro Negro has composition akin to true melt represented by the inclusions. The variations of the bulk magma (rocks) and melt (melt inclusions) compositions can be generated in a dyke connecting a deep primitive magma reservoir with the Cerro Negro edifice. While the melt inclusions represent the compositional trend of instantaneous melts along the magma pathway at decreasing pressure and H2O content, occurrence of low-Mg to high-Mg basalts reflects the process of phenocryst re-distribution in progressively evolving melt. The crystallization scenario is anticipated to operate everywhere in dykes feeding basaltic volcanoes and can explain the predominance of plagioclase-rich high-Al basalts in island arc as well as typical compositional variations of magmas during single eruptions.  相似文献   

13.
Abstract Fluid evolution paths in the COHN system can be calculated for metamorphic rocks if there are relevant data regarding the mineral assemblages present, and regarding the oxidation and nitrodation states throughout the entire P-T loop. The compositions of fluid inclusions observed in granulitic rocks from Rogaland (south-west Norway) are compared with theoretical fluid compositions and molar volumes. The fluid parameters are calculated using a P-T path based on mineral assemblages, which are represented by rocks within the pigeonite-in isograd and by rocks near the orthopyroxene-in isograd surrounding an intrusive anorthosite massif. The oxygen and nitrogen fugacities are assumed to be buffered by the coexisting Fe-Ti oxides and Cr-carlsbergite, respectively. Many features of the natural fluid inclusions, including (1) the occurrence of CO2-N2-rich graphite-absent fluid inclusions near peak M2 metamorphic conditions (927° C and 400 MPa), (2) the non-existence of intermediate ternary CO2-CH4-N2 compositions and (3) the low-molar-volume CO2-rich fluid inclusions (36–42 cm3 mol?1), are reproduced in the calculated fluid system. The observed CO2-CH4-rich inclusions with minor N2 (5 mol%) should also include a large proportion of H2O according to the calculations. The absence of H2O from these natural high-molar-volume CO2-CH4-rich inclusions and the occurrence of natural CH4-N2-rich inclusions are both assumed to result from preferential leakage of H2O. This has been previously experimentally demonstrated for H2O-CO2-rich fluid inclusions, and has also been theoretically predicted. Fluid-deficient conditions may explain the relatively high molar volumes, but cannot be used to explain the occurrence of CH4-N2-rich inclusions and the absence of H2O.  相似文献   

14.
To assess further the role of pore fluids in enhancing mass transport in deep-seated rocks, bulk diffusion coefficients (D-values) for chlorine have been measured at 1.0 GPa and 1000°C in texturally-equilibrated quartzites containing varying amounts (0.3–2.8 vol%) of H2O or a CO2–H2O mixture (X CO2=0.4). Experiments were used to monitor transport predominantly through the fluid phase by employing a chemical tracer dissolved in the fluid (chlorine) that is virtually insoluble in the rock matrix (quartzite) but is somewhat soluble in a small fraction of dispersed indicator minerals (fluorapatite). For diffusion in H2O-bearing quartzite, experiments with 1 vol.% fluid exhibit a continuous decrease in D-values with decreasing porosity whereas an abrupt drop in the diffusion coefficient is indicated by the experiments with 0.3 vol.% fluid. At a given total porosity, diffusion coefficients obtained from quartzites containing the CO2–H2O fluid range from 80x to > 3000x lower than those from H2O-bearing experiments. Bulk transport measurements were correlated with textural observations and the observed reduction in bulk D-values for quartzites containing the CO2–H2O fluid reflects the overall isolated nature of porosity in such samples. The drop in the bulk D-value for quartzites with 0.3 vol.% H2O probably arises from the elimination of interconnected porosity owing to the presence of a sufficient number of dry grain edges. Textural observations, combined with transport measurements, are consistent with the pore structure predicted by dihedral angle measurements. However, due to anisotropy in the interfacial energy of quartz, long-range fluid connectivity is dramatically reduced in quartzites with low H2O contents, despite a median dihedral angle of less than (but near) 60°. Observed variations in chlorine D-values in samples with connected and non-connected porosity are found to be consistent with previous bulk property measurements on texturally-equilibrated, fluid-bearing rocks. Results of this study, combined with prior bulk diffusion measurements for oxygen, provides a general assessment of the effect of small amounts of fluid on the enhancement of mass transport in quartzose lithologies over a range of crustal P and T. At conditions of textural equilibrium, it is expected that the fluid phase provides little or no contribution to the long-range diffusive flux of solutes in quartz-rich rocks containing small amounts of H2O or CO2–H2O mixtures.  相似文献   

15.
Reactions and partial melting of peraluminous rocks in the presence of H2O-CO2–salt fluids under parameters of granulite-facies metamorphism were modeled in experiments on interaction between orthopyroxene–cordierite–biotite–plagioclase–quartz metapelite with H2O, H2O-CO2, H2O-CO2-NaCl, and H2O-CO2-KCl fluids at 600 MPa and 850°C. Rock melting in the presence of H2O and equimolar H2O-CO2 fluids generates peraluminous (A/CNK1 > 1.1) melts whose composition corresponds to magnesian calcic or calc–alkaline S-type granitoids. The melts are associated with peritectic phases: magnesian spinel and orthopyroxene containing up to 9 wt % Al2O3. In the presence of H2O-CO2-NaCl fluid, cordierite and orthopyroxene are replaced by the association of K-Na biotite, Na-bearing gedrite, spinel, and albite. The Na2O concentrations in the biotite and gedrite are functions of the NaCl concentrations in the starting fluid. Fluids of the composition H2O-CO2-KCl induce cordierite replacement by biotite with corundum and spinel and by these phases in association with potassium feldspar at X KCl = 0.02 in the fluid. When replaced by these phases, cordierite is excluded from the melting reactions, and the overall melting of the metapelite is controlled by peritectic reactions of biotite and orthopyroxene with plagioclase and quartz. These reactions produce such minerals atypical of metapelites as Ca-Na amphibole and clinopyroxene. The compositions of melts derived in the presence of salt-bearing fluids are shifted toward the region with A/CNK < 1.1, as is typical of so-called peraluminous granites of type I. An increase in the concentrations of salts in the fluids leads to depletion of the melts in Al2O3 and CaO and enrichment in alkalis. These relations suggest that the protoliths of I-type peraluminous granites might have been metapelites that were melted when interacting with H2O-CO2-salt fluids. The compositions of the melts can evolve from those with A/CNK > 1.1 (typical of S-type granites) toward those with A/CNK = 1.0–1.1 in response to an increase in the concentrations of alkali salts in the fluids within a few mole percent. Our experiments demonstrate that the origin of new mineral assemblages in metapelite in equilibrium with H2O-CO2-salt fluids is controlled by the activities of alkaline components, while the H2O and CO2 activities play subordinate roles. This conclusion is consistent with the results obtained by simulating metapelite mineral assemblages by Gibbs free energy minimization (using the PERPE_X software), as shown in log(\({a_{{H_2}O}}\))–log(\({a_{N{a_2}O}}\)) and log(\({a_{{H_2}O}}\))–log(\({a_{{K_2}O}}\)) diagrams.  相似文献   

16.
Fluorine contents in about 300 samples of various types of basalts and related rocks from continental (southwestern U.S.A.; Zaire; Deccan and South Africa) and oceanic regions (Hawaii and Mid-Atlantic Ridge between 23° N and 40° N) were determined by a selective ion-electrode method.Of all of the major components in these basaltic rocks, F shows good correlation only with K2O. It increases regularly from tholeiite to perpotassic basalt on continents, and from tholeiite to nephelinite on Hawaii. In the F-K2O diagram all the basaltic rocks from continents and Hawaii plot between the origin of the coordinate axes and the field of phlogopite in peridotite xenoliths in South African kimberlites. Accordingly, the major proportions of F, K2O and also H2O in these basaltic magmas are derived from phlogopite at the source regions in the upper mantle. On the other hand, F in abyssal tholeiites is relatively higher than that of the other tholeiites at equal K2O content, and it is suggested that most of F, K2O and H2O are derived from pargasites.When it is assumed that the upper mantle phlogopite contains about 10% K2O, 0.4% (0.3–0.5%) F and 4% H2O, H2O content in basaltic magmas from continental including island arc and oceanic island regions can be qualitatively estimated based on their proportions of K2OFH2O. Similarly, H2O content in abyssal basaltic rocks is also estimated on the basis of FH2O in pargasites (Table 2).A suite of Deccan tholeiites shows remarkable F enrichment with increasing K2O due to separation of anhydrous and K-free minerals during fractionation. F in tholeiitic and alkali basalt magmas in Hawaii also increases regularly with K2O during progressive fractionation until the later stages, where rhyodacite and trachyte exhibit a relative decrease owing to the effective subtraction of F-bearing amphibole and apatite in addition to anhydrous minerals.  相似文献   

17.
The early miocene Tecuya volcanic center in the southern San Joaquin basin of California consists of flows and tuffs of basalt and rhyolite that erupted, closely spaced in time, in both submarine and subaerial conditions. The rhyolites are overlain by the basalts and constitute approximately 45% of a total of at least 180 km3 of the Tecuya volcanic rocks. The basalts have Nd(t) values of +2 to +6 and (87Sr/86Sr)i values between 0.7035 and 0.7052. These rocks show LREE enrichment [(La/Yb)N =2.4–5.5; La=28–150 times chondrite] and higher Th/U, Th/Ta, Rb/Ta, Ba/Ta, Cs/Rb but lower K/Rb ratios than MORB. Combined major- and trace-element, and Sr–Nd isotopic data suggest the involvement of subcontinental lithosphere, depleted upper mantle source (MORB), and local continental crust in the basalt petrogenesis. Nd(t) values in rhyolites vary from +1.5 to +3.7 while (87Sr/86Sr)i ratios range from 0.7051 to 0.7064. The rhyolites display LREE enrichment [(La/Yb)N=10; La=100 times chondrite] along with a distinct negative Eu anomaly (Eu/Eu*=0.75) and depletion of Ti and P. Mixing relations in (87/86Sr)i – Nd(t) space among basalts, rhyolites, and local continental crust indicate that the Tecuya rhyolites were produced by assimilation of variable amounts of continental crust by MORB-related magmas and subcontinental lithosphere-derived melts. This conclusion is supported by the synchroneity of Tecuya volcanism at 22 Ma with interaction of a segment of the East Pacific Rise along the southern California margin. The Tecuya volcanic rocks thus provide an example for the generation of rhyolitic melts owing to crustal assimilation by basaltic melts during mid-oceanic ridge-induced magmatism along a continental margin.  相似文献   

18.
Petrographic evidence is presented for the breakdown of titanian hydroxyl-clinohumite to olivine+magnesian ilmenite (or geikielite)±magnetite in the outermost zone of the Bergell aureole in the Malenco Serpentinite, Prov. Sondrio, Italy. The breakdown coincides in the field with the isograd reaction: antigorite+diopside=olivine+tremolite+H2O. It is therefore concluded that this variety of clinohumite is unstable above approximately 520° C at a pressure of 3 kbars. Elsewhere in the Malenco Serpentinite, titanian hydroxyl-clinohumite may be found to have reacted with CO2 to produce antigorite, magnesian ilmenite and magnesite. Titanian hydroxyl-chondrodite was detected in one sample. Under crustal pressures, the stability field of F-free clinohumite is entirely contained inside that of antigorite. The stable occurrence of titanian clinohumite in high-grade metamorphic ultrabasic rocks may be attributed to the substitution of F for OH.  相似文献   

19.
Melt and fluid inclusions were investigated in minerals from igneous rocks and ore (Au-Ag-Pb-Zn) veins of the Stiavnica ore field in Central Slovakia. High H2O (7.1–12.0 wt %) and Cl (0.32–0.46 wt %) contents were found in silicate melt inclusions (65–69 wt % SiO2 and 5.2–5.6 wt % K2O) in plagioclase phenocrysts (An 68–36) from biotite-homblende andesites of the eastern part of the caldera. Similar high water contents are characteristic of magmatic melts (71–76 wt % SiO2 and 3.7–5.1 wt % K2O) forming the sanidine rhyolites of the Vyhne extrusive dome in the northwestern part of the Stiavnica caldera (up to 7.1 wt %) and the rhyolites of the Klotilda dike in the eastern part of the ore field (up to 11.5 wt %). The examination of primary inclusions in quartz and sanidine from the Vyhne rhyolites revealed high concentrations of N2 and CO2 in magmatic fluid (8.6 g/kg H2O and 59 g/kg H2O, respectively). Fluid pressure was estimated as 5.0 kbar on the basis of primary CO2 fluid inclusions in plagioclase phenocrysts from the Kalvari basanites. This value corresponds to a depth of 18 km and may be indicative of a deep CO2 source. Quartz from the granodiorites of the central part of the Stiavnica-Hodrusa complex crystallized from a melt with 4.2–6.1 wt % H2O and 0.24–0.80 wt % Cl. Magmatic fluid cogenetic with this silicate melt was represented by a chloride brine with a salinity of no less than 77–80 wt % NaCl equiv. Secondary inclusions in quartz of the igneous rocks recorded a continuous trend of temperature, pressure, and solution salinity, from the parameters of magmatic fluids to the conditions of formation of ore veins. The gold mineralization of the Svyatozar vein system was formed from boiling low-salinity fluids (0.3–8.0 wt % NaCl equv.) at temperatures of 365–160°C and pressures of 160–60 bar. The Terezia, Bieber, Viliam, Spitaler, and Rozalia epithermal gold-silver-base metal veins were also formed from heterogeneous low-salinity fluids (0.3–12.1 wt %) at temperatures of 380–58°C and pressures of 240–10 bar. It was found that the salt components of the solutions were dominated by chlorides (high content of fluorine, up to 0.45 mol/kg H2O, was also detected), and sulfate solutions appeared in the upper levels. The dissolved gas of ore-forming solutions was dominated by CO2 (0.1–8.4 mol %, averaging 1.3 wt %) and contained minor nitrogen (0.00–0.85 mol %, averaging 0.05 mol %) and negligible methane admixtures (0.00–0.05 mol %, averaging 0.004 mol %). These data allowed us to conclude that the magmatic melts could be sources of H2O, Cl, CO2, and N2. The formation of the epithermal mineralization of the Stiavnica ore field was associated with the mixing of magmatic fluid with low-concentration meteoric waters, and the fluid was in a heterogeneous state.  相似文献   

20.
《Applied Geochemistry》1988,3(5):499-516
“Stratabound” disseminated pyritic Au ore bodies were produced by reactions between wall rocks and through-flowing fluids in Mesozoic epigenetic Au quartz vein systems in the Sierra Nevada metamorphic belt. Equilibrium relations among Fe-bearing carbonate and sulfide minerals were critical in determining which rock types were likely to host disseminated mineralization along portions of discordant veins. The compositions of metasomatic carbonates in hydrothermally altered wall rocks at Alleghany, California, U.S.A., were larely predetermined by the relative proportions of Fe, Mg and Ca in the unaltered wall rocks. Thus, coexisting solid solutions in the magnesite-siderite and dolomite-ankerite series from a variety of different wall rocks yield an empirical phase diagram for a large part of the Ca CO3MgCO3FeCO3 system at the temperature of metasomatism (325 ± 50°C). Because Fe,Mg-silicates were unstable in alteration zones adjacent to the veins, wall rock Fe was partitioned between carbonates and sulfides. Pyritization and disseminated Au mineralization occur in a variety of igneous and metasedimentary wall rocks in which the initial molar Fe/(Fe + Mg) ≧ 0.5. In altered wall rocks with initial molar Fe/(Fe + Mg) ≦ 0.5, Fe was incorporated almost entirely within Mg-rich carbonates (XFeCO3 ≦ 0.6 in magnesite-siderite solutions). It is proposed that the CO2-rich vein fluid responsible for the alteration and mineralization was partially buffered with respect to H2S/CO2/H2 ratios by equilibrium between pyrite and Mg0.4Fe0.6CO3 (+graphite?) as it traversed and altered intermediate volcanic and sedimentary rocks. This fluid then locally reacted with lower Fe/(Fe + Mg) rocks to form Fe-bearing dolomite + magnesite assemblages, and reacted with higher Fe/(Fe + Mg) rocks to form ankerite + pyrite assemblages. Gold precipitated from saturated solutions of bisulfide complexes partly in response to fluid desulfidation and reduction caused by the pyritization reactions. In terranes dominated by intermediate metavolcanic and metasedimentary rocks, favorable host rocks for this type of mineralization need not have high Fe contents, but do require high Fe/(Fe + Mg) ratios. They may include felsic volcanic and plutonic rocks, Fe-rich tholeiitic differentiates, banded Fe formations, and a variety of siliceous and argillaceous sedimentary rocks. Rocks which tend not to be heavily sulfidized because they have low initial Fe/(Fe + Mg) ratios include ultramafic and mafic igneous rocks, and some argillaceous sedimentary rocks. Exploration guidelines based on these principles may be useful elsewhere in the Sierra Nevada and in other comparable heterogeneous metamorphic terranes, if modified to reflect the dominant buffering rock types in a given fluid flow path. Carbonate-sulfide equilibria are capable of approximately buffering the carbonate-sulfide ratios of CO2-rich vein fluids (fCO2≧ 102.8 at 325°C, 200MPa or 2000 bar). The Alleghany fluid (fCO2 ≈ 103.2, or ∼ 10 mol % CO2) had a molar CO2/H2S ratio of approximately 103, assuming graphite saturation. At lower CO2 fugacities, Fe-bearing silicates entered the buffering assemblages. Carbonatization reactions could potentially de-sulfidize some wall rocks, releasing S (and associated metals?) to the fluid. This would be most likely to occur in pyrite-bearing mafic and ultramafic rocks and some argillites.  相似文献   

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