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1.
Interleaved phyllosilicate grains (IPG) of various compositions are widespread in low-grade Verrucano metasediments of the northern Apennines (Italy). They are ellipsoidal or barrel shaped, up to 300–400 μm long and they are often kinked and folded; phyllosilicate packets occur as continuous lamellae or as wedge-shaped layers terminating inside the grain. Using electron microscopy techniques (SEM, TEM) six types of IPG have been distinguished on the basis of their mineralogical composition: (1) Chl+Ms ± Kln; (2) Chl+ Ms+Pg ± Kln; (3) Ms+Prl ± Pg; (4) Ms+Prl+Su; (5) Ms+Prl+Chl+Su; (6) Su+Ms. Types (1) and (2) are mainly composed of chlorite, with Ms and Pg as minor phases; Kln grows on Ms in highly weathered samples. Types (3), (4), (5), and (6) are composed of muscovite, with intergrown Prl, Chl, Su and new-formed muscovite. The IPG show all kinds of contacts: from coherent grain boundaries with parallel basal planes and along-layer transitions to low- and high-angle grain boundaries. The IPG formed on pristine minerals such as chlorite and muscovite. The transformations took place during the prograde and retrograde metamorphic path of the rocks: they were facilitated by deformation and they occurred in equilibrium with a fluid phase, which allowed cation diffusion. Prograde reactions [Chl = Ms (or Pg); Ms = Prl; Ms = Chl] involve dehydration and sometimes a decrease in volume, whereas retrograde reactions (Ms = Kln; Ms = Su) involve hydration and an increase in volume. These transformations do not simply occur through an interchange of cations, but often involve deep structural changes: transitions from one phyllosilicate to another generally proceed through dissolution-recrystallization reactions. In conclusion, Verrucano IPG represent microstructural sites which have not completely equilibrated with the whole rock and whose mineral assemblage depends on the original composition of the microstructural sites. Received: 20 June 1996 / Accepted: 3 February 1997  相似文献   

2.
Anhydrite-bearing dolomites and kimberlites from the contact zone of the Udachnaya Vostochnaya pipe, northern part of the Eastern Siberian Platform, were affected by low-grade metamorphism to the zeolite facies. The kimberlites are serpentinized and carbonatized and contain metasomes of anhydrite and saponite pockets. Twenty lizardite pseudomorphs after olivine (Fo 91–82) in the kimberlites were examined on an electron microprobe. The lizardite is rimmed by saponite and contains dolomite, calcite, magnetite, and anhydrite inclusions. Lizardite in the central parts of the pseudomorphs contains 1.5–1.9 wt % Cl and 6–9 wt % Fe2O3, and this mineral in the outer portions of the pseudomorphs bears 0.7–1.0 wt % Cl and 2–6 wt % Fe2O3 (the paper presents nine microprobe analyses and images showing the distribution of Cl, Mg, Al, Si, S, Ca, Ti, and Fe obtained in characteristic X-ray radiation). The amounts of Fe3+ in octahedrally and tetrahedrally coordinated sites of the Cl-bearing lizardite are roughly equal. Cl was borrowed in the course of serpentinization from the host Early Paleozoic evaporites and brines contained in them. The Cl concentration in our lizardite from the metamorphosed kimberlites from the Eastern Siberian Platform (continental lizardite) is much higher than the Cl concentration in oceanic lizardite from serpentine replacing peridotites (0.03–0.2 wt % Cl). This is likely explained by differences in the Cl concentrations in the metamorphic fluids, their salinity (3% for oceanic water and 65% for brines in the platform cover).  相似文献   

3.
The stratiform Cu–Co ore mineralisation in the Katangan Copperbelt consists of dispersed sulphides and sulphides in nodules and lenses, which are often pseudomorphs after evaporites. Two types of pseudomorphs can be distinguished in the nodules and lenses. In type 1 examples, dolomite precipitated first and was subsequently replaced by Cu–Co sulphides and authigenic quartz, whereas in type 2 examples, authigenic quartz and Cu–Co sulphides precipitated prior to dolomite and are coarse-grained. The sulphur isotopic composition of the copper–cobalt sulphides in the type 1 pseudomorphs is between −10.3 and 3.1‰ relative to the Vienna Canyon Diablo Troilite, indicating that the sulphide component was derived from bacterial sulphate reduction (BSR). The generation of during this process caused the precipitation and replacement of anhydrite by dolomite. A second product of BSR is the generation of H2S, resulting in the precipitation of Cu–Co sulphides from the mineralising fluids. Initial sulphide precipitation occurred along the rim of the pseudomorphs and continued towards the core. Precipitation of authigenic quartz was most likely induced by a pH decrease during sulphide precipitation. Fluid inclusion data from quartz indicate the presence of a high-salinity (8–18 eq. wt.% NaCl) fluid, possibly derived from evaporated seawater which migrated through the deep subsurface. 87Sr/86Sr ratios of dolomite in type 1 nodules range between 0.71012 and 0.73576, significantly more radiogenic than the strontium isotopic composition of Neoproterozoic marine carbonates (87Sr/86Sr = 0.7056–0.7087). This suggests intense interaction with siliciclastic sedimentary rocks and/or the granitic basement. The low carbon isotopic composition of the dolomite in the pseudomorphs (−7.02 and −9.93‰ relative to the Vienna Pee Dee Belemnite, V-PDB) compared to the host rock dolomite (−4.90 and +1.31‰ V-PDB) resulted from the oxidation of organic matter during BSR.  相似文献   

4.
Lattice Preferred Orientation (LPO) of quartz and muscovite are measured in a micaceous quartzite using SEM based Electron Backscatter Diffraction (EBSD) analysis. The measurements were done in a thin section prepared parallel to the K1K3 plane of the anisotropy of magnetic susceptibility (AMS) ellipsoid, which is equivalent to the XZ plane of the strain ellipsoid. Bulk data from the sample reveal that quartz c-axis develop an oblique single girdle LPO pattern indicating a dextral sense of shear. A similar pattern is produced by poles to the basal planes (001) of muscovite, which implies that muscovite controls the LPO of quartz in the rock. Petrofabric analysis of quartz is performed in domains viz. (I) not containing muscovite, (II) between two muscovite grains, and (III) rim of quartz grains around a muscovite grain. Quartz LPO pattern in Domain-III is noted to be similar to the bulk LPO recorded from the whole sample, thus confirming that muscovite was critical in textural evolution of the rock. The study thus establishes that a minor mineral phase in a rock can control the LPO of the major mineral phase, thus playing a significant role in development of bulk texture of the rock. The advantages of domainal petrofabric analysis in evaluation of slip systems in minerals in different parts of a rock, and vorticity quantification are discussed.  相似文献   

5.
 Coexisting muscovite and paragonite have been observed in an eclogite from the Sesia–Lanzo Zone (Western Alps, Italy). The P-T conditions of this eclogite reached 570–650 °C and 19–21 kbar and the rocks show several stages of mineral growth during their retrograde path, ranging from the subsequent lower-P eclogite facies to the blueschist facies and then the greenschist facies. Muscovite and paragonite are very common in these rocks and show two texturally different occurrences indicating equilibrium and non-equilibrium states between them. In one mode of occurrence they coexist in equilibrium in the lower-P eclogite facies. In the same rock muscovite ± albite also replaced paragonite during a greenschist-facies overprint, as evidenced by unique across – (001) layer boundaries. The chemical compositions of the lower-P eclogite-facies micas plot astride the muscovite – paragonite solvus, whereas the compositions of the greenschist-facies micas lie outside the solvus and indicate disequilibrium. The TEM observations of the textural relations of the greenschist-facies micas imply structural coherency between paragonite and muscovite along the layers, but there is a sharp discontinuity in the composition of the octahedral and tetrahedral sheets across the phase boundary. We propose that muscovite formed through a dissolution and recrystallization process, since no gradual variations toward the muscovite – paragonite interfaces occur and no intermediate, homogeneous Na-K phase has been observed. Because a solid-state diffusion mechanism is highly unlikely at these low temperatures (300–500 °C), especially with respect to octahedral and tetrahedral sites, it is assumed that H2O plays an important role in this process. The across-layer boundaries are inferred to be characteristic of such non-equilibrium replacement processes. The characterization of these intergrowths is crucial to avoiding erroneous assumptions regarding composition and therefore about the state of equilibrium between both micas, which in turn may lead to misinterpretations of thermometric results. Received: 3 February 1999 / Accepted: 19 October 1999  相似文献   

6.
 The surface structure of the tetrahedral sheet of dioctahedral mica muscovite was compared to that of the tetrahedral sheet of trioctahedral mica phlogopite using atomic force microscopy (AFM). AFM revealed distinct structural differences between the tetrahedral sheet surfaces of the two micas. The hexagonal ring in the AFM image of muscovite elongates in the [3 1 0] direction, and the groove runs perpendicular to the [3 1 0] direction. On the phlogopite surface, the hexagonal ring contracts slightly in the a axis direction, but the groove is not apparent. These results were consistent with the bulk structure data of the two micas determined by X-ray diffraction (XRD). The degree of surface relaxation was much larger in muscovite than in phlogopite. In muscovite, the interlayer K reduces the amount of tetrahedral rotation that actually occurs, since the interlayer K is too large for its hexagonal hole after full tetrahedral rotation. Thus, it is naturally expected that muscovite will show more tetrahedral rotation after removal of the interlayer K. It is also expected that muscovite will show more tilting of SiO4 tetrahedra after cleaving, since an attractive force between the hydrogen in the OH group and the lower basal oxygen should be in operation, due to the decreased distance between them following interlayer K removal. Received: 14 March 2000 / Accepted: 29 July 2000  相似文献   

7.
In quartz-free Fe, Na-poor and high-Mg, Al schists from the Bundelkhand craton in north central India, corundum porphyroblasts in finely interleaved phlogopite–chlorite aggregates with rare clinozoisite are mantled by fine-grained (<3 μm) intergrowths of outer collars (>200 μm wide) of phengitic-muscovite and chlorite (phlogopite + corundum + H2O → phengitic-muscovite + chlorite), and <100 μm wide inner collars of margarite–muscovite (corundum + clinozoisite + phengitic muscovite → margarite + muscovite + H2O). Wide-beam electron probe microanalyses indicate Mg in the bi-layered corona increases from corundum outwards, with a complementary decrease in Al and K. Si and Ca increase and then decrease to matrix values. The sharp chemical gradients across the highly structured bi-layered corona are inferred to suggest that the corona-forming reactions were promoted by local grain-boundary-controlled thermodynamic instability as opposed to element transport by advective diffusion. The P–T convergence of KMASH reactions and NCKMASH pseudosection phase relations computed using micro-domain compositions indicate the chlorite–phengitic muscovite outer collar formed at 18–20 kbar and ca. 630°C. The NCKMASH margarite–muscovite inner collar yielded lower metamorphic P–T conditions of 11 ± 3 kbar, ca. 630°C. U–Th–Pb chemical dating of metamorphic monazite and LA-ICPMS U–Pb isotope dating of re-equilibrated zircon yield ca. 2.78 Ga ages, which are interpreted to date corona formation and Neoarchean high-P metamorphism in the Bundelkhand craton, hitherto unknown in the Indian Precambrian. (220)  相似文献   

8.
The Brandberg West region of NW Namibia is dominated by poly-deformed turbidites and carbonate rocks of the Neoproterozoic Damara Supergoup, which have been regionally metamorphosed to greenschist facies and thermally metamorphosed up to mid-amphibolite facies by Neoproterozoic granite plutons. The meta-sedimentary rocks host Damaran-age hydrothermal quartz vein-hosted Sn–W mineralization at Brandberg West and numerous nearby smaller deposits. Fluid inclusion microthermometric studies of the vein quartz suggests that the ore-forming fluids at the Brandberg West mine were CO2-bearing aqueous fluids represented by the NaCl–CaCl2–H2O–CO2 system with moderate salinity (mean=8.6 wt% NaClequivalent).Temperatures determined using oxygen isotope thermometry are 415–521°C (quartz–muscovite), 392–447°C (quartz–cassiterite), and 444–490°C (quartz–hematite). At Brandberg West, the oxygen isotope ratios of quartz veins and siliciclastic host rocks in the mineralized area are lower than those in the rocks and veins of the surrounding areas suggesting that pervasive fluid–rock interaction occurred during mineralization. The O- and H-isotope data of quartz–muscovite veins and fluid inclusions indicate that the ore fluids were dominantly of magmatic origin, implying that mineralization occurred above a shallow granite pluton. Simple mass balance calculations suggest water/rock ratios of 1.88 (closed system) and 1.01 (open system). The CO2 component of the fluid inclusions had similar δ 13C to the carbonate rocks intercalated with the turbidites. It is most likely that mineralization at Brandberg West was caused by a combination of an impermeable marble barrier and interaction of the fluids with the marble. The minor deposits in the area have quartz veins with higher δ 18O values, which is consistent with these deposits being similar geological environments exposed at higher erosion levels.  相似文献   

9.
In this study, reservoir temperatures of Balıkesir geothermal waters in northwestern Turkey are estimated with various geochemical models. The geothermal fluids in the region are represented by Na–SO4, Na–HCO3 and Ca–HCO3 type waters with discharge temperatures up to 98°C. It was determined that the solubility of silica in most of the waters is controlled by the chalcedony phase. Equilibrium states of the Balıkesir thermal waters studied by means of Na–K–Mg–Ca diagram, mineral saturation calculations and activity diagrams in the system composed of Na2O–CaO–K2O–Al2O3–SiO2–H2O phases approximate a reservoir temperature of about 120°C. Most of the waters are found to be equilibrated with calcite, chalcedony ± quartz and muscovite at predicted temperature ranges, similar to those calculated from the chemical geothermometers.  相似文献   

10.
Dehydration kinetics of muscovite by in situ infrared microspectroscopy   总被引：2，自引：0，他引：2  
Dehydration behavior of muscovite flake was investigated at 760–860°C by using in situ high-temperature IR microspectroscopy for the OH absorption band around 3,620 cm−1. Isothermal kinetic heating experiments at each temperature gave detailed decrease curves of the OH band area with time. These curves have been simulated by the first and second order reactions or mono- and two-dimensional diffusion processes. The mono-dimensional diffusion was found to give the best fit to the experimental data and apparent diffusion coefficients D were determined at 760–860°C with the activation energy of 290 ± 20 kJ/mol. The apparent diffusion coefficients D varied with the sample thickness L. This variation can be explained by an m layers model with a unit length of L′ with a constant diffusion coefficient D′. Therefore, the dehydration process might be rate-limited by mono-dimensional diffusion through tetrahedral silicate sheet perpendicular to (001) planes of muscovite with a unit length of L′.  相似文献   

11.
Effects of H2O on the Disequilibrium Breakdown of Muscovite+Quartz   总被引：1，自引：0，他引：1  
We have examined in detail the effect of H2O on the texturesand mechanisms produced during the breakdown of muscovite+quartzunder experimental disequilibrium conditions using low-porosityrock samples. Under H2O conditions (1 wt.% H2O added) muscovitereacts completely in <5 months at 757?C to a metastable assemblageof peraluminous meltmullite+biotite, a reaction which delaysthe formation of the stable equilibrium assemblage. In contrast,muscovite in the H2O undersaturated experiments breaks downby both the stable dehydration reaction producing K feldspar+sillimanite+biotiteand by metastable melting reactions in the same sample. Thecom position of the metastable melt is controlled by a numberof kinetic factors which change as a function of time and reactionprogress. Early melts are highly siliceous and sodic due tothe rapid dissolution of quartz relative to muscovite, coupledwith the incongruent melting of the paragonite component ofmuscovite and crystallization of biotite. The delayed nucleationof mullite results in Al supersaturation of the melt, whichinhibits the rate of the melting reaction. Once mullite nucleatesthe degree of Al melt supersaturation is decreased and the rateof muscovite dissolution increases. After complete reactionof muscovite the melt chemistry continues to change as Si diffusesinto the pseudomorphs from adjacent quartz. Even after 5 monthsat 757?C large compositional gradients in Si and Al still persistwithin the melt. In the H2O experiments metastable melting occursinitially, catalysed by traces of grain boundary fluid or byfluid released from the dehydration of muscovite. However, oncemelting starts any fluid is strongly fractionated into the meltphase, reducing µH2O Under these conditions further meltingis inhibited and the stable dehydration reaction will continue.Examination of examples of natural muscovite reacted under disequilibriumconditions in xenolithic and contact metamorphic rocks at lowpressures suggests that metastable melting is an important processunder certain geological conditions. It is possible that itis widespread in contact metamorphic rocks, but the texturesindicative of metastable melting reactions are obscured duringthe extended cooling histories of such rocks.  相似文献   

12.
The transformations (density, composition, or shape alterations) of fluid inclusions under isobaric cooling and isothermal compression have been experimentally modeled. The H2O-CO2-CH4 inclusions used in the model experiments have been synthesized in quartz at 1 or 3 kbar and 700°C. The parameters of the model experiments were as follows: for isobaric cooling, 700–400°C at 1 or 3 kbar; for isothermal compression, 1–3 and 3–5 kbar at 400 and 700°C, respectively. The shape of the inclusion walls changed as a result of the experiments because of the dissolution and reprecipitation of the host phase. The intensity of these changes was directly affected by the pressure and temperature differences and the amount of the aqueous phase in the inclusions. Fluid densities increased in many inclusions in the run products: the increase ranged from insignificant (0.06 g/cm3) to fairly noticeable (0.15 g/cm3). The composition of the fluid inclusions also changed. The results of the experiments, in particular of those carried out with a labeled fluid, show that the penetration of a denser external fluid into inclusions with a lower fluid density is the basic reason for the increase in the density and change in the composition of fluid inclusions. In several experiments, the methane concentration changed with an attendant change in the melting temperature of carbon dioxide but without noticeable changes in the carbon dioxide homogenization temperature. Original Russian Text ? O.V. Vasyukova, V.I. Fonarev, 2006, published in Geokhimiya, 2006, No. 12, pp. 1266–1278.  相似文献   

13.
Preservation of partially completed metamorphic reactions in the form of partial pseudomorphs is very important as it provides direct insight onto the reaction mechanism and the phases involved in the reaction. The staurolite and andalusite grade rocks in western Maine, USA, contain cordierite porphyroblasts partly pseudomorphed by coarse-grained muscovite and biotite. The pseudomorphs consist of a cordierite core surrounded by a reaction rim. Modal mineralogy, calculated using the ImageJ processing software based on backscatter images and X-ray compositional maps, reveals that the core consists of cordierite (53.5%), muscovite (22.8%), biotite (9.1%), quartz (1 0.4%), plagioclase (3.1%) and ilmenite/pyrrhotite and apatite (1.1%) whereas the reaction rim consists of cordierite (1.8%), muscovite (51.6%), biotite (30.4%), quartz (4.3%), plagioclase (10%), garnet (1.2%), ilmenite/pyrrhotite and apatite (0.8%). The net effect of the cordierite breakdown reaction is an increase of 226% in muscovite, 334% in biotite and 323% in plagioclase content and a decrease of 97% in cordierite. The reaction involved exchange of components with the matrix requiring addition of H2O, K+, Na+ and Ti4+ and removal of SiO2, Mg2+ and PO43- from the reaction site. PT estimates using the garnet–biotite, Ti-in-biotite, Na-in-cordierite thermometers and the garnet–biotite–muscovite–plagioclase barometer indicate that cordierite breakdown occurred at ~550°C and 3.5 kbar. thermocalc modelling using the bulk rock composition suggests that cordierite is not stable at these conditions, whereas modelling using a thin section-derived bulk composition indicates that cordierite stability extends to higher pressures, and most likely that the cordierite breakdown was not PT dependent. The incorporation of Na (up to 0.18 a.f.u.) into the cordierite structure has the effect of stabilizing the cordierite under a variety of H2O activity and limiting the role of fluids into destabilizing it. The cordierite cores contain evidence of plastic and brittle deformation in the form of subgrains and microcracks, which facilitated the infiltration of fluids that destabilized cordierite at constant PT conditions by leaching Na and introducing K. New mica growth along these structural heterogeneities suggests that deformation played an important role promoting breakdown of cordierite to muscovite and biotite.  相似文献   

14.
The surface structure of muscovite was imaged using an atomic force microscope (AFM) in contact mode in water. The following three types of AFM images were observed: (1) those showing clearly the arrangement of hexagonal rings of SiO4 tetrahedra; (2) those showing a hexagonal array of bright spots separated by a distance of about 5.3 Å; and (3) those changing gradually from image (2) to image (1). Image (1) successfully provides information on the tetrahedral tilt and basal surface corrugation that are particularly characteristic of dioctahedral micas. The mean unit cell dimensions for the muscovite surface measured from Image (1) were slightly longer than those of the bulk structure, due to the rehydration of the tetrahedral sheet and/or surface relaxation. Image (2) was made by varying the scan angles, even on the same surface in which Image (1) was obtained. Image (3) has information on a single plane rather than on two or more planes involving steps, kinks and so on. Therefore, what is depicted in Images (2) and (3) is not the arrangement of interlayer K ions but the basal plane of the tetrahedral sheet. Some structural relaxation of the tetrahedral sheet surface was also observed. Gradual expansion and contraction of hexagonal rings were randomly found on the muscovite surface. The surface relaxation results from a tetrahedral rotation and/or tilting after cleaving, since significant variations of both distances and bond angles between adjacent SiO4 tetrahedra on the surface were found.  相似文献   

15.
Scheelite-mineralized microtonalite sheets occur on the SE margin of the end-Caledonian Leinster Granite in SE Ireland. Scheelite, polymetallic sulphides and minor cassiterite occur in veins in the microtonalites, disseminated throughout the greisened microtonalite sheets and in the adjacent wallrocks. Two major mineralized vein types occur in the microtonalite sheets: (1) Scheelite ± arsenopyrite ± pyrrhotite occur in quartz-fluorite veins, generally without a muscovite selvage; (2) Sphalerite ± chalcopyrite ± pyrite ± galena ± cassiterite ± stannite occur in quartz + fluorite veins with a coarse muscovite selvage and are often intergrown with the muscovite. Quartz-hosted fluid inclusions were examined from representative samples of both vein types using petrographic, microthermometric and laser Raman spectroscopic techniques. Three distinct types of fluid inclusions have been recognized. Primary, vapour rich Type 1 inclusions in quartz from the scheelite-mineralized veins are of H2O-CO2-CH4-N2 ± H2S ± NaCl composition and formed between 360–530 °C. Primary and secondary, liquid-rich Type 2 fluid inclusions in the base metal sulphide-mineralized veins are of H2O-CH4-N2 ± H2S-NaCl composition and formed between 340–480 °C. They also occur as pseudosecondary and secondary inclusions in scheelite-mineralized veins. Late dilute, low temperature H2O-NaCl + KCl fluid inclusions may be related to late-Caledonian convection of meteoric waters around the cooling Leinster Granite batholith. Received: 4 September 1996 / Accepted: 23 May 1997  相似文献   

16.
Sediment instabilities are common on the prodeltas of the seismically active continental margins of Western Greece. Sediment failures on the low-angle (0.5°–2°) prodelta slopes manifest themselves as successions of peripheral rotational block slumps restricted to the foresets of the late highstand systems tract (HST). The individual slump blocks are about 80–150 m long and are bounded by growth faults acting as curved slip planes that extend to a mean depth of 10–15 m below seafloor. Shear planes develop in the lower part of muddy and/or gas charged HST foresets. Deeper basal transparent muddy layers of the early HST bottomset, together with the late Pleistocene transgressive systems tract sequences (TST), are mostly unaffected. On the steeper (2°–6°) fan delta slopes of the western Gulf of Corinth debris flows and avalanches with a significant retrogressive component dominate slope destabilisation. Sediment cores taken from landslide scarps and slide planes penetrated gas bubble releasing sediments thereby indicating that failure planes are in the late HST foresets/upper part of the early HST bottomsets gas charged zone. The foresets of the HST prodelta deposits display high water content (30–80%), low bulk density (1.4–1.9 g cm−3) and relatively low values of undrained shear strength (3–20 kPa). The water content of the HST distal muddy bottomsets is relatively higher (50–110%) and bulk density relatively lower (1.3–1.7 g cm−3) with low values of shear strength (2–10 kPa). The shear strength of the gas releasing sediment layer displays lower values (2–9 kPa) relative to the overlying, post failure, muddy sediments of the late 100–300 years. Slope stability was calculated using the normalised soil parameter (NSP) method under undrained conditions for normally consolidated prodelta sediments. This analysis indicates that instabilities could be induced by critical earthquake ground accelerations of 26.6–29.6% g for the HST foresets and 12.4–14.1% g for the basal transparent layer belonging to the early HST bottomsets. Consequently the early HST bottomsets has to be considered a potentially unstable layer since the regional peak ground accelerations (PGAs) for the next 50 years are expected to range from 19 to 30% g. Moreover, our results show that new glide planes in the prodeltaic sediment bodies of the seismically active continental margins of Western Greece will likely develop from the gas charged sediments of the lower part of the HST foresets to the upper part of early HST bottomsets.  相似文献   

17.
The beginning of melting in the system Qz-Or-Ab-An-H2 O was experimentally reversed in the pressure range kbar using starting materials made up of mixtures of quartz and synthetic feldspars. With increasing pressure the melting temperature decreases from 690° C at 2 kbar to 630° C at 17 kbar in the An-free alkalifeldspar granite system Qz-Or-Ab-H2O. In the granite system Qz-Or-Ab-An-H2O the increase of the solidus temperature with increasing An-content is only very small. In comparison to the alkalifeldspar granite system the solidus temperature increases by 3° C (7° C) if albite is replaced by plagioclase An 20 (An 40). The difference between the solidus temperatures of the alkalifeldspar granite system and of quartz — anorthite — sanidine assemblages (system Qz-Or-An-H2O) is approximately 50° C. With increasing water pressures plagioclase and plagioclase-alkalifeldspar assemblages become unstable and are replaced by zoisite+kyanite+quartz and zoisite+muscovite-paragonitess +quartz, respectively. The pressure stability limits of these assemblages are found to lie between 6 and 16 kbar at 600° C. At high water pressures (10–18 kbar) zoisite — muscovite — quartz assemblages are stable up to 700 and 720° C. The solidus curve of this assemblage is 10–20° C above the beginning of melting of sanidine — zoisite — muscovite — quartz mixtures. The amount of water necessary to produce sufficient amounts of melt to change a metamorphic rock into a magmatic looking one is only small. In case of layered migmatites it is shown that 1 % of water (or even less) is sufficient to transform portions of a gneiss into (magmatic looking) leucosomes. High grade metamorphic rocks were probably relatively dry, and anatectic magmas of granitic or granodioritic composition are usually not saturated with water.  相似文献   

18.
A kyanite mine in central Virginia produces a silicate-rich waste stream which accumulates at a rate of 450,000–600,000 tons per year. An estimated 27 million tons of this waste stream has accumulated over the past 60 years. Grain size distribution varies between 1.000 and 0.053 mm, and is commonly bimodal with modes typically being 0.425 and 0.250 mm and uniformity coefficients vary from 2.000 to 2.333. Hydraulic conductivity values vary from 0.017 to 0.047 cm/s. Mineralogy of the waste stream consists of quartz, muscovite, kyanite and hematite. Muscovite grains have distinct chemical compositions with significant Na2O content (1.12–2.66 wt%), TiO2 content (0.63–1.68 wt% TiO2) and Fe content, expressed as Fe2O3 (up to 1.37 wt%). Major element compositions of samples were dominated by SiO2 (87.894–90.997 wt%), Al2O3 (6.759–7.741 wt%), Fe2O3 (1.136–1.283 wt%), and K2O (0.369–0.606 wt%) with other components being <1.000 wt%. Elements of environmental concern (V, Cr, Ni, Cu, Zn, As, Ag, Sn, Sb, Ba, Hg, Tl, and Pb) were detected; however, the concentrations of all elements except Ni were below that of the kyanite quartzites in the region from which the waste is derived. Both major and trace element compositions indicate minimal variation in composition. The waste stream has potential for recycling. Muscovite is suitable for recycling as a paint pigment or other industrial applications. Muscovite and hematite are commonly intergrown and are interpreted to be material where much of the elements of environmental concern are concentrated. Reprocessing of the waste stream to separate muscovite from other components may enable the waste stream to be used as constructed wetland media for Virginia and nearby states. Recycling of this mine waste may have a positive impact on the local economy of Buckingham County and aid in mitigation of wetland loss.  相似文献   

19.
《Journal of Structural Geology》2002,24(6-7):1139-1156
In metapelitic rocks of western Maine, a pluton-related M3 metamorphic gradient ranging in grade from garnet to upper sillimanite zone was superposed on a fairly uniform M2 regional metamorphic terrain characterized by the assemblage andalusite+staurolite+biotite+/−garnet. As a result, M2 assemblages re-equilibrated to the P, T, and aH2O conditions of M3, and both prograde and retrograde pseudomorphism of M2 porphyroblasts occurred. The type of pseudomorph and degree of development is directly related to the rock's position within the M3 metamorphic gradient, a function of its proximity to the Mooselookmeguntic pluton. Several ‘hinge’ zones occur in which the M3 minerals that pseudomorphed a particular M2 phase change. For example, M2 garnet was replaced by M3 chlorite or biotite, depending on its position within the M3 gradient. Similarly, in a transition zone between M3 upper staurolite and lower sillimanite zones, M2 staurolite was stable and shows M3 growth rims. Downgrade from this transition zone, staurolite was pseudomorphed by chlorite and muscovite, whereas upgrade, the pseudomorphs contain muscovite and some biotite. M3 pseudomorphs commonly retain crystal shapes of the original M2 porphyroblasts, reflecting relatively low regional deviatoric stress during and after M3. Although evidence for textural disequilibrium is common, chemical equilibrium was closely approached during M3. This study demonstrates for M3 that: (1) the pseudomorphic replacement was a constant volume process, and (2) fabrics produced by tectonic events can be erased by subsequent deformation and/or sufficiently intense subsequent recrystallization.  相似文献   

20.
This paper deciphers the late stress systems involved in the development of kink bands in the perspective of thrust regime. In kink bands, the correlation coefficient for α–β plots is positive near thrusts and negative away from thrusts. The plots show nearly linear relationship near thrusts and non-linear relationship away from thrusts. The rotation was prominent mechanism of kink band formation near thrusts and rotation coupled with shearing, along the kink planes away from thrusts. Along thrusts σ 1 is horizontal E–W trend and it rotates to horizontal N–S trend away from the thrust. The proposed model establishes that (1) the shearing along kink planes led to angular relationship, β < α and (2) the kink planes of conjugate kinks could be used for paleostress analysis even in those cases where shearing along these planes has occurred.  相似文献   

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