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1.
Near the eastern end of the Tonale fault zone, a segment of the Periadriatic fault system in the Italian Alps, the Adamello intrusion produced a syn-kinematic contact aureole. A temperature gradient from 250 to 700 °C was determined across the Tonale fault zone using critical syn-kinematic mineral assemblages from the metasedimentary host rocks surrounding deformed quartz veins. Deformed quartz veins sampled along this temperature gradient display a transition from cataclasites to mylonites (frictional–viscous transition) at 280±30 °C. Within the mylonites, zones characterized by different dynamic recrystallization mechanisms were defined: Bulging recrystallization (BLG) was dominant between 280 and 400 °C, subgrain rotation recrystallization (SGR) in the 400–500 °C interval, and the transition to dominant grain boundary migration recrystallization (GBM) occurred at 500 °C. The microstructures associated with the three recrystallization mechanisms and the transitions between them can be correlated with experimentally derived dislocation creep regimes. Bulk texture X-ray goniometry and computer-automated analysis of preferred [c]-axis orientations of porphyroclasts and recrystallized grains are used to quantify textural differences that correspond to the observed microstructural changes. Within the BLG- and SGR zones, porphyroclasts show predominantly single [c]-axis maxima. At the transition from the SGR- to the GBM zone, the texture of recrystallized grains indicates a change from [c]-axis girdles, diagnostic of multiple slip systems, to a single maximum in Y. Within the GBM zone, above 630±30 °C, the textures also include submaxima, which are indicative of combined basal a- and prism [c] slip.  相似文献   

2.
Fluid inclusions in the metamorphic aureole of the Eureka Valley‐Joshua Flat‐Beer Creek (EJB) pluton in the White‐Inyo Range, California, reveal the compositions and origin of fluids that were present during variable recrystallization of quartzite with sedimentary grain shapes to metaquartzite with granoblastic texture. Metamorphosed sedimentary formations, including quartzites, marbles, calcsilicates and schists, became ductile and strongly attenuated in the aureole during growth of the magma chamber. The microstructures of quartzites have an unusual distribution in that within ~250 m from the pluton, where temperatures exceeded 650 °C, they exhibit relict sedimentary grain shapes, only small amount of grain boundary migration (GBM), and crystallographic preferred orientations (CPOs) dominated by <a> slip. At distances >250 m, quartzites were completely recrystallized by GBM and CPOs are indicative of prism [c] slip, characteristics that are typically associated with H2O‐assisted, high‐T recrystallization. The lack of extensive GBM in the inner aureole can be attributed to rapid replacement of H2O by CO2 produced by reaction of quartz grains with calcite cement that also produced interstitial wollastonite. Fluid inclusions in the inner aureole generally occur in margins of quartz grains and are either wholly aqueous (Type 1) or also contain H2S, CO2 and CH4 (Type 2). Type 2 inclusions occur only in some stratigraphic layers. In both inclusion types, NaCl and CaCl2, in variable proportions, dominate the solutes in the aqueous phase, whereas FeCl2 and KCl are less abundant solutes. The solutes indicate attainment of a degree of equilibrium with carbonates and schists that are interbedded with the quartzites. Some Types 1 and 2 inclusions in the inner aureole show evidence of decrepitation due to high amounts of strain and/or heating suffered by the host rocks, which suggests that they represent pore fluids that existed in the rocks prior to contact metamorphism. In addition to Type 1 inclusions, outer aureole quartzites also contain inclusions that contain CO2 vapour bubbles in addition to aqueous phase (Type 3). These inclusions only occur in interiors of granoblastic quartz that was produced by large amounts of GBM. The aqueous phase has identical ranges of first melting and final ice melting temperatures as Type 1 inclusions, suggesting that they have the same solute compositions. These inclusions are thought to represent the interstitial pore H2O that promoted recrystallization of quartz and reacted with graphite to produce CO2. Absence of significant amounts of CH4 in Type 3 inclusions is attributed to elevated fO2 that was buffered by mineral assemblages in interbedded schists. As opposed to the large amount of CO2 that was produced by the wollastonite‐forming reaction in the inner aureole to inhibit GBM, the amount of CO2 produced in the outer aureole by reaction between H2O and graphite was apparently insufficient to inhibit recrystallization of quartz.  相似文献   

3.
Anisotropy of magnetic susceptibility (AMS) in micaceous quartzites with mean susceptibility (K m) >50 × 10−6 SI units is known to be on account of the orientation distribution of the para/ferromagnetic minerals (e.g. micas, magnetite), which comprise the minor phase in the rocks. However, the strain in such deformed micaceous quartzites is dominantly accommodated by the quartz grains, which are the major phase in them. The objective of this paper is to explore the extent to which AMS data from micaceous quartzites provide information about the shape of the strain ellipsoid. AMS analysis of 3 quartzite blocks is performed, and the shape of the AMS ellipsoid is recorded to be oblate. From AMS data, the three principal planes of the AMS ellipsoid are identified in each block and thin sections are prepared along them. Quartz grain shape (aspect ratio, R q), intensity of quartz and mica shape preferred orientation (κq and κmi, respectively) and 2D strain (E) recorded by quartz are measured in each section. R q, κq, κmi and E are all noted to be minimum in the section parallel to the magnetic foliation plane as compared to the other two sections. This indicates that the quartz grains have oblate shapes in 3D and accommodated flattening strain, which is similar to the shape of the AMS ellipsoid. The role of mica in causing Zener drag and pinning of quartz grain boundaries is discussed. It is concluded that during progressive deformation, migration of pinned grain boundaries is inhibited. This causes enhanced recrystallization at the grain boundaries adjacent to the pinned ones, thus guiding the shape modification of quartz grains. A strong correlation is demonstrated between κq and κmi as well as κmi and E. It is inferred that fabric evolution of quartz was controlled by mica. Hence, the shape of the AMS ellipsoid, which is on account of mica, provides information about shape of the strain ellipsoid.  相似文献   

4.
Dynamic recrystallization in the strict sense of the term is the reconstitution of crystalline material without a change in chemical composition, driven by strain energy in the form of dislocations. Driving potentials additional to internal strain energy may contribute to the recrystallization of naturally deformed minerals, which form solid solutions such as feldspar, amphiboles and pyroxenes, if they change their composition during recrystallization. To estimate the relative importance of these driving potentials, the chemical composition of porphyroclasts and recrystallized grains of plagioclase, clinopyroxene and hornblende have been investigated in samples from a high grade shear zone of the Ivrea Zone, Italy. The plagioclases show two different recrystallization microstructures: bulging recrystallization at grain boundaries and discrete zones of recrystallized grains across porphyroclasts probably involving fracturing. Deformation took place under amphibolite facies conditions on a retrograde P,T-path. Porphyroclast and recrystallized compositions from bulging recrystallization microstructures differ only in their Or-content and yield a ΔG between mean host grain and mean recrystallized grain composition at fixed P,T-conditions of approximately 5 Joules/10−4 m3. Extreme compositional variations yield approximately 60 J/10−4 m3. The increase of free energy due to dislocations calculated for common glide systems in plagioclase are on the order of 100 Joules/10−4 m3 for high values of dislocation densities of 1014 m−2. Thus, the effect of chemically induced driving energies on grain boundary velocity appears small for mean compositions but may be as great as that of deformational energies for larger chemical differences. In the other type of microstructure, porphyroclasts and recrystallized grains in discrete zones differ in their anorthite content. The maximum ΔG induced by the compositional disequilibrium is on the order of 100 J/10−4 m3. This maximum value is of the same magnitude as the ΔG derived from high dislocation densities of 1014 m−2. The resulting combined ΔG is approximately twice as high as for deformational ΔG alone, and heterogeneous nucleation may become a feasible recrystallization mechanism which is evident from the microstructures. The recrystallization mechanism depends on the nature of the driving potential. Grain boundary migration (GBM) and heterogeneous nucleation can release Gibbs free energy induced by compositional disequilibrium, whereas this is not likely for subgrain rotation. Therefore, only GBM and heterogeneous nucleation may link metamorphism and deformation, so that syndeformational recrystallization may represent a transitional process ranging from dynamic recrystallization to metamorphic reaction. Received: 8 July 1996 / Accepted: 17 November 1997  相似文献   

5.
In the present study, the grain size (d) and shape of 225 magnetite grains, that crystallized at T>600°C in a syntectonic granite (Godhra Granite, India) are evaluated and implications of data to decipher deformation mechanism of magnetite are discussed. Fractal (ruler) dimension (D) analysis of magnetite grains is performed and it is demonstrated that they show fractal behaviour. Smaller magnetite grains tend to be more serrated than the larger ones, which is manifested in the higher fractal (ruler) dimension (D) of the former. Assuming a natural strain rate ranging between 10−10 s−1 and 10−14 s−1, the grain size data fall dominantly in the dislocation creep field of the existing deformation mechanism map of magnetite for 630°C. However, SEM-EBSD studies reveal that subgrains are absent in the magnetite grains and they did not undergo dislocation creep. Thus it is inferred that the shape of magnetite grains was not controlled by dislocation creep. It is concluded that the higher serration and increased fractal dimension of finer magnetite grains implies the importance of diffusion creep as an important deformation mechanism at high-T for magnetite in polymineralic rocks.  相似文献   

6.
Fluid inclusions in granite quartz and three generations of veins indicate that three fluids have affected the Caledonian Galway Granite. These fluids were examined by petrography, microthermometry, chlorite thermometry, fluid chemistry and stable isotope studies. The earliest fluid was a H2O-CO2-NaCl fluid of moderate salinity (4–10 wt% NaCl eq.) that deposited late-magmatic molybdenite mineralised quartz veins (V1) and formed the earliest secondary inclusions in granite quartz. This fluid is more abundant in the west of the batholith, corresponding to a decrease in emplacement depth. Within veins, and to the east, this fluid was trapped homogeneously, but in granite quartz in the west it unmixed at 305–390 °C and 0.7–1.8 kbar. Homogeneous quartz δ18O across the batholith (9.5 ± 0.4‰n = 12) suggests V1 precipitation at high temperatures (perhaps 600 °C) and pressures (1–3 kbar) from magmatic fluids. Microthermometric data for V1 indicate lower temperatures, suggesting inclusion volumes re-equilibrated during cooling. The second fluid was a H2O-NaCl-KCl, low-moderate salinity (0–10 wt% NaCl eq.), moderate temperature (270–340 °C), high δD (−18 ± 2‰), low δ18O (0.5–2.0‰) fluid of meteoric origin. This fluid penetrated the batholith via quartz veins (V2) which infill faults active during post-consolidation uplift of the batholith. It forms the most common inclusion type in granite quartz throughout the batholith and is responsible for widespread retrograde alteration involving chloritization of biotite and hornblende, sericitization and saussuritization of plagioclase, and reddening of K-feldspar. The salinity was generated by fluid-rock interactions within the granite. Within granite quartz this fluid was trapped at 0.5–2.3 kbar, having become overpressured. This fluid probably infiltrated the Granite in a meteoric-convection system during cooling after intrusion, but a later age cannot be ruled out. The final fluid to enter the Granite and its host rocks was a H2O-NaCl-CaCl2-KCl fluid with variable salinity (8–28 wt% NaCl eq.), temperature (125–205 °C), δD (−17 to −45‰), δ18O (−3 to + 1.2‰), δ13CCO2 (−19 to 0‰) and δ34Ssulphate (13–23‰) that deposited veins containing quartz, fluorite, calcite, barite, galena, chalcopyrite sphalerite and pyrite (V3). Correlations of salinity, temperature, δD and δ18O are interpreted as the result of mixing of two fluid end-members, one a high-δD (−17 to −8‰), moderate-δ18O (1.2–2.5‰), high-δ13CCO2 (> −4‰), low-δ34Ssulphate (13‰), high-temperature (205–230 °C), moderate-salinity (8–12 wt% NaCl eq.) fluid, the other a low-δD (−61 to −45‰), low-δ18O (−5.4 to −3‰), low-δ13C (<−10‰), high-δ34Ssulphate (20–23‰) low-temperature (80–125 °C), high-salinity (21–28 wt% NaCl eq.) fluid. Geochronological evidence suggests V3 veins are late Triassic; the high-δD end-member is interpreted as a contemporaneous surface fluid, probably mixed meteoric water and evaporated seawater and/or dissolved evaporites, whereas the low-δD end-member is interpreted as a basinal brine derived from the adjacent Carboniferous sequence. This study demonstrates that the Galway Granite was a locus for repeated fluid events for a variety of reasons; from expulsion of magmatic fluids during the final stages of crystallisation, through a meteoric convection system, probably driven by waning magmatic heat, to much later mineralisation, concentrated in its vicinity due to thermal, tectonic and compositional properties of granite batholiths which encourage mineralisation long after magmatic heat has abated. Received: 3 April 1996 / Accepted: 5 May 1997  相似文献   

7.
Three reactions limiting the stability field of the di-trioctahedral chlorite cookeite in the presence of quartz, in the system Li2O−Al2O3−SiO2−H2O (LASH) have been reversed in the range 290–480°C, 0.8–14 kbar, using natural material close to the end member composition. Combining our results with known and estimated thermodynamic properties of the other minerals belonging to the LASH system, the enthalpy (-8512200 J/mol) and the entropy (504.8 J/mol*K) of cookeite are calculated by a feasible solution space approach. The knowledge of these values allowed us to draw the first P−T phase diagram involving both the hydrated Li-aluminosilicates cookeite and bikitaite, which is applicable to a large variety of natural rock systems. The low thermal extent of the stability field of cookeite+quartz (260–480°C) makes cookeite a valuable indicator of low temperature conditions within a wide range of pressure (1–14 kbar).  相似文献   

8.
This study focuses on the retrograde rheological and chemical evolution of quartz and the behaviour of quartzites during retrograde metamorphism following dry high grade metamorphism at 750°C, 7 kbar. SEM-CL and LA-HR-ICP-MS are applied to document quartz texture and chemistry, respectively. Four generations of quartz were distinguished by SEM-CL; Qz1, Qz2, Qz3 and Qz4. Qz1, brecciated and partly dissolved old grains, is enriched in B, Al and Ti when compared with the other types. Qz2, formed during brecciation and partial dissolution of Qz1, has low Al contents (<50 ppm) but, due to rutile inclusions, variable Ti contents when occurring in amphibolite (210–10 ppm) but more consistent values when occurring in quartzites (peak value 32 ppm). Qz3, dark grey luminescent quartz forming fluid migration channels (fluid pathways), has Ti < 5 ppm and Al contents below 10 ppm and B < 1 ppm. Qz4, comprises are group of quartz later than Qz3 filling micron thick cracks and pods with very low luminescent quartz, i.e. darker than Qz3. The textural and chemical evolution of quartz in our study is explained by two major influxes of aqueous fluids during regional uplift and retrogression. They facilitated rehydration and recrystallisation in the otherwise dry high grade quartzites. The first introduction of aqueous fluids was associated with brecciation of the high grade quartz (Qz1) and dissolution/precipitation of quartz (Qz2). Ti in quartz geothermometry (Wark and Watson, Contrib Mineral Petrol 152(6):637–652) gives 626°C in agreement with the retrograde PT-path deduced from phase diagrams. Later fluid influx associated with scapolitisation of amphibolite caused localised recrystallisation (Qz3) and alteration of biotite to muscovite along mm-wide fluid migration channels. During subsequent deformation, Qz3 deformed plastically and recovered by subgrain rotation recrystallisation (SGR), resulting in a reduction of grain size, whereas Qz1 quartz formed micro faults. Qz2 was plastic but did not experience SGR to the same degree as Qz3 quartz. Increased plasticity and recovery rates most likely relate to an increased H2O fugacity and the depletion in trace elements of the quartz lattice by promoting strain softening processes dislocation climb and recovery. Electronic supplementary material  The online version of this article (doi:) contains supplementary material, which is available to authorized users.  相似文献   

9.
At Malanjkhand, Central India, lode-type copper (-molybdenum) mineralization occurs within calcalkaline tonalite-granodiorite plutonic rocks of early Proterozoic age. The bulk of the mineralization occurs in sheeted quartz-sulfide veins, and K-silicate alteration assemblages, defined by alkali feldspar (K-feldspar ≫ albite) + dusty hematite in feldspar ± biotite ± muscovite, are prominent within the ore zone and the adjacent host rock. Weak propylitic alteration, defined by albite + biotite + epidote/zoisite, surrounds the K-silicate alteration zone. The mineralized zone is approximately 2 km in strike length, has a maximum thickness of 200 m and dips 65°–75°, along which low-grade mineralization has been traced up to a depth of about 1 km. The ore reserve has been conservatively estimated to be 92 million tonnes with an average Cu-content of 1.30%. Supergene oxidation, accompanied by limited copper enrichment, is observed down to a depth of 100m or more from the surface. Primary ores consist essentially of chalcopyrite and pyrite with minor magnetite and molybdenite. δ34S (‰) values in pyrite and chalcopyrite (−0.38 to +2.90) fall within the range characteristic of granitoid-hosted copper deposits. δ18O (‰) values for vein quartz (+ 6.99 to +8.80) suggest exclusive involvement of juvenile water. Annealed fabrics are common in the ore. The sequence of events that led to the present state of hypogene mineralization is suggested to be as follows: fracturing of the host rock, emplacement of barren vein quartz, pronounced wall-rock alteration accompanied by disseminated mineralization and the ultimate stage of intense silicification accompanied by copper mineralization. Fragments of vein quartz and altered wall rocks and striae in the ore suggest post-mineralization deformation. The recrystallization fabric, particularly in chalcopyrite and sphalerite, is a product of dynamic recrystallization associated with the post-mineralization shearing. The petrology of the host rocks, hydrothermal alteration assemblages, ore mineral associations, fluid inclusions and the sulfur and oxygen isotopes of ores are comparable to those in Phanerozoic (and reported Precambrian) porphyry-copper systems, and the Malanjkhand deposit has important implications for both metallogenic models for, and mineral exploration in, Precambrian terrains.  相似文献   

10.
New mineralogical, thermobarometric, isotopic, and geochemical data provide evidence for long and complex formation history of the Sarylakh and Sentachan Au-Sb deposits conditioned by regional geodynamics and various types of ore mineralization, differing in age and source of ore matter combined in the same ore-localizing structural units. The deposits are situated in the Taryn metallogenic zone of the East Yakutian metallogenic belt in the central Verkhoyansk-Kolyma Fold Region. They are controlled by the regional Adycha-Taryn Fault Zone that separates the Kular-Nera Terrane and the western part of the Verkhoyansk Fold-Thrust Belt. The fault extends along the strike of the northwest-trending linear folds and is deep-rooted and repeatedly reactivated. The orebodies are mineralized crush zones accompanied by sulfidated (up to 100 m wide) quartz-sericite metasomatic rocks and replacing dickite-pyrophyllite alteration near stibnite veinlets. Two stages of low-sulfide gold-quartz and stibnite mineralization are distinguished. The formation conditions of the early milk white quartz in orebodies with stibnite mineralization at the Sarylakh and Sentachan deposits are similar: temperature interval 340–280°C, salt concentration in fluids 6.8–1.6 wt % NaCl equiv, fluid pressure 3430–1050 bar, and sodic bicarbonate fluid composition. The ranges of fluid salinity overlapped at both deposits. In the late regenerated quartz that attends stibnite mineralization, fluid inclusions contain an aqueous solution with salinity of 3.2 wt % NaCl equiv and are homogenized into liquid at 304–189°C. Syngenetic gas inclusions contain nitrogen 0.19 g/cm3 in density. The pressure of 300 bar is estimated at 189°C. The composition of the captured fluid is characterized as K-Ca bicarbonatesulfate. The sulfur isotopic composition has been analyzed in pyrite and arsenopyrite from ore and metasomatic zones, as well as in coarse-, medium-, and fine-grained stibnite varieties subjected to dynamometamorphism. The following δ34S values, ‰ have been established at the Sarylakh deposit: −2.0 to −0.9 in arsenopyrite, −5.5 to −1.1 in pyrite, and −5.5 to −3.6 in stibnite. At the Sentachan deposit: −0.8 to +1.0 in arsenopyrite, +0.5 to +2.6 in pyrite, and −3.9 to +0.6 in stibnite. Sulfides from the Sentachan deposit is somewhat enriched in 34S. The 18O of milk white quartz at the Sarylakh deposit varies from +14.8 to 17.0‰ and from +16.4 to + 19.3‰ at the Sentachan. The δ18O of regenerated quartz is +16.5‰ at the Sarylakh and +17.6 to +19.8‰ at the Sentachan. The δ18O of carbonates varies from +15.0 to 16.3% at the Sarylakh and from +16.7 to +18.2‰ at the Sentachan. The δ13C of carbonates ranges from −9.5 to −12.1‰ and −7.8 to −8.5‰, respectively. The calculated $ \delta ^{18} O_{H_2 O} $ \delta ^{18} O_{H_2 O} of the early fluid in equilibrium with quartz and dolomite at 300δC are +7.9 to +10.1‰ for the Sarylakh deposit and +9.5 to +12.4‰ for the Sentachan deposit (+4.9 and 6.0‰ at 200°C for the late fluid, respectively). Most estimates fall into the interval characteristic of magmatic water (°18O = +5.5 to +9.5‰).  相似文献   

11.
The Darreh Sary metapelitic rocks are located in the northeast of Zagros orogenic belt and Sanandaj-Sirjan structural zone. The lithological composition of these rocks includes slate, phyllite, muscovitebiotite schist, garnet schist, staurolite-garnet schist and staurolite schist. The shale is the protolith of these metamorphic rocks, which was originated from the continental island arc tectonic setting and has been subjected to processes of Zagros orogeny. The deformation mechanisms in these rocks include bulging recrystallization (BLG), subgrain rotation recrystallization (SGR) and grain boundary migration recrystallization (GBM), which are considered as the key to estimate the deformation temperature of the rocks. The estimated ranges of deformation temperature and depth in these rocks show the temperatures of 275–375, 375–500, and >500°C and the depths of 10 to 17 km. The observed structures in these rocks such as faults, fractures and folds, often with the NW-SE direction coordinate with the structural trends of Zagros orogenic belt structures. The S-C mylonite fabrics is observed in these rocks with other microstructures such as mica fish, σ fabric and garnet deformation indicate the dextral shear deformation movements of study area. Based on the obtained results of this research, the stages of tectonic evolution of Darreh Sary area were developed.  相似文献   

12.
The Assif El Mal Zn–Pb (Cu–Ag) vein system, located in the northern flank of the High Atlas of Marrakech (Morocco), is hosted in a Cambro-Ordovician volcaniclastic and metasedimentary sequence composed of graywacke, siltstone, pelite, and shale interlayered with minor tuff and mudstone. Intrusion of synorogenic to postorogenic Late Hercynian peraluminous granitoids has contact metamorphosed the host rocks giving rise to a metamorphic assemblage of quartz, plagioclase, biotite, muscovite, chlorite, amphibole, chloritoid, and garnet. The Assif El Mal Zn–Pb (Cu–Ag) mineralization forms subvertical veins with ribbon, fault breccia, cockade, comb, and crack and seal textures. Two-phase liquid–vapor fluid inclusions that were trapped during several stages occur in quartz and sphalerite. Primary inclusion fluids exhibit T h mean values ranging from 104°C to 198°C. Final ice-melting temperatures range from −8.1°C to −12.8°C, corresponding to salinities of ∼15 wt.% NaCl equiv. Halogen data suggest that the salinity of the ore fluids was largely due to evaporation of seawater. Late secondary fluid inclusions have either Ca-rich, saline (26 wt.% NaCl equiv.), or very dilute (3.5 wt.% NaCl equiv.) compositions and homogenization temperatures ranging from 75°C to 150°C. The δ18O and δD fluid values suggest an isotopically heterogeneous fluid source involving mixing between connate seawater and black-shale-derived organic waters. Low δ13CVPDB values ranging from −7.5‰ to −7.7‰ indicate a homogeneous carbon source, possibly organic matter disseminated in black shale hosting the Zn–Pb (Cu–Ag) veins. The calculated δ34SH2S values for reduced sulfur (22.5‰ to 24.3‰) are most likely from reduction of SO4 2− in trapped seawater sulfate or evaporite in the host rocks. Reduction of sulfate probably occurred through thermochemical sulfate reduction in which organic matter was oxidized to produce CO2 which ultimately led to precipitation of saddle dolomite with isotopically light carbon. Lead isotope compositions are consistent with fluid–rock interaction that leached metals from the immediate Cambro-Ordovician volcaniclastic and metasedimentary sequence or from the underlying Paleo-Neoproterozoic crustal basement. Geological constraints suggest that the vein system of Assif El Mal formed during the Jurassic opening of the central Atlantic Ocean.  相似文献   

13.
The Jinshan orogenic gold deposit is a world-class deposit hosted by a ductile shear zone caused by a transpressional terrane collision during Neoproterozoic time. Ore bodies at the deposit include laminated quartz veins and disseminated pyrite-bearing mylonite. Most quartz veins in the shear zone, with and without gold mineralization, were boudinaged during progressive shear deformation with three generations of boudinage structures produced at different stages of progressive deformation. Observations of ore-controlling structures at various scales indicate syn-deformational mineralization. Fluid inclusions from pyrite intergrown with auriferous quartz have 3He/4He ratios of 0.15–0.24 Ra and 40Ar/36Ar ratios 575–3,060. δ18Ofluid values calculated from quartz are 5.5–8.4‰, and δD values of fluid inclusions contained in quartz range between −61‰ and −75‰. The δ13C values of ankerite range from −5.0‰ to −4.2‰, and ankerite δ18O values from 4.4‰ to 8.0‰. The noble gas and stable isotope data suggest a predominant crustal source of ore fluids with less than 5% mantle component. Data also show that in situ fluids were generated locally by pervasive pressure solution, and that widespread dissolution seams acted as pathways of fluid flow, migration, and precipitation. The in situ fluids and fluids derived from deeper levels of the crust were focused by deformation and deformation structures at various scales through solution-dissolution creep, crack-seal slip, and cyclic fault-valve mechanisms during progressively localized deformation and gold mineralization.  相似文献   

14.
The greenschist to amphibolite transition as modeled by the reaction zoisite+tremolite + quartz= anorthite+diopside+water has been experimentally investigated in the chemical system H2O−CaO− MgO−Al2O3−SiO2 over the range of 0.4–0.8 GPa. This reaction is observed to lie within the stability fields of anorthite + water and of zoisite + quartz, in accord with phase equilibrium principles, and its position is in excellent agreement with the boundary calculated from current internally-consistent data bases. The small dP/dT slope of 0.00216 GPa/K (21.6 bars/K) observed for this reaction supports the pressure-dependency of this transition in this chemical system. Experimental reversals of the Al content in tremolitic amphibole coexisting with zoisite, diopside, quartz, and water were obtained at 600, 650, and 700°C and indicated Al total cations (atoms per formula unit, apfu) of only up to 0.5±0.08 at the highest temperature. Thermodynamic analysis of these and previous compositional reversal data for tremolitic amphibole indicated that, of the activity/composition relationships considered, a two-site-coupled cation substitution model yielded the best fit to the data and a S 0 (1 bar, 298 K) of 575.4±1.6 J/K · mol for magnesio-hornblende. The calculated isopleths of constant Al content in the amphibole are relatively temperature sensitive with Al content increasing with increasing temperature and pressure. Finally, several experiments in the range of 1.0–1.3 GPa were conducted to define the onset of melting, and thus the upper-thermal limit, for this mineral assemblage, which must involve an invariant point located at approximately 1.05 GPa and 770°C. Received: 24 January 1997 / Accepted: 2 October 1997  相似文献   

15.
秦岭伏牛山构造带的矿物岩石学特征与流变学分析   总被引：1，自引：0，他引：1       下载免费PDF全文
本文通过对伏牛山构造带岩石的矿物岩石学、石英重结晶型式、石英分维值和有限应变等特征分析研究,认为伏牛山构造带的变质-变形深受洛南-栾川断裂带的影响,其变化有明显的规律性,从断裂带往北岩石从糜棱岩依次过渡为片岩-片麻岩-花岗岩原岩.构造带内发育多种糜棱岩,岩石变形强烈,远离构造带岩石的变形逐渐变弱.从构造带往北,石英的重...  相似文献   

16.
 The hitherto unknown low-temperature heat capacity of nickel chromite (NiCr2O4) was measured between 8 and 381 K using adiabatic calorimetry, and some thermochemical functions [CP(T), S(T), S°298, H(T)−H(0)] were derived from the results. The standard entropy (S°298=140.0 ± 0.3 J mol−1 K−1) for nickel chromite was calculated from the results. Our calorimetric measurements indicate three major anomalies in the heat-capacity curve at temperatures between 8 and 381 K. A short literature review indicates that two of these anomalies can be accounted for, whereas an anomaly peaking at 29 K has not been reported previously.  相似文献   

17.
The dissolved fluoride (F−) in the Lower Ganges-Brahmaputra-Meghna (GBM) river system, Bengal basin, Bangladesh, was studied during 1991–1993 to determine its distribution and source in the basin, and its annual flux to the Bay of Bengal. The concentration of dissolved F− varied between 2 and 11 μmol l−1 with statistically significant variations both spatially and temporally in the basin. Such variations are attributable to the geology of the individual subbasins (Ganges, Brahmaputra and Meghna), dilution by rainwater during monsoon and groundwater contribution to the river systems during dry season. Correlation coefficients among F− and major cations and anions suggest diverse inorganic processes responsible for regulating the concentration of F− in these river systems. However, fluorite seems to be one of the major sources of dissolved F−. The concentration of F− in the Lower GBM river system is low compared to the rivers draining Deccan Plateau and arid regions of the subcontinent, for example, Yamuna and its tributaries. However, it is within the range of most of the other Peninsular and Himalayan rivers. The GBM system contributes about 115×103 tonnes year−1 of dissolved F− into the Bay of Bengal, and thus accounts for about 3% of the global F− flux to the oceans annually. Received: 19 May 1999 · Accepted: 11 October 1999  相似文献   

18.
五莲拆离断层带中石英韧性变形明显,在野外主要表现为条带状、拔丝状,显微镜下主要表现为多晶石英条带,发育亚颗粒旋转重结晶和膨凸重结晶,剪切带经历了中低温条件下的变形,变形温度为300～450℃。利用分形方法对石英颗粒边界的研究表明,发生动态重结晶的石英颗粒边界具有统计学意义上的自相似性和明显的分形特征,亚颗粒旋转重结晶石英颗粒分维数介于1. 260～1. 319之间,均值1. 276;膨凸重结晶石英颗粒的分维数为1. 217～1. 297,均值为1. 256;根据石英粒径估算出亚颗粒旋转重结晶和膨凸重结晶作用变形阶段的古差异应力,分别为7. 84～21. 58MPa和18. 51～56. 65 MPa;基于分维值计算的应变速率计算公式,获得亚颗粒旋转与膨凸重结晶石英颗粒的应变速率分别为10-8. 4～10-7. 7s-1、10-10. 5～10-9. 7s-1;基于石英流变率计算,亚颗粒旋转重结晶的石英应变速率介于10-12. 88～10-11. 73s-1之间,膨凸重结晶的为10-13. 72～10-12. 46s-1。本地区韧性变形的应变速率大于一般性韧性剪切带应变速率,可能与拆离断层带的快速拆离伸展作用有关。  相似文献   

19.
Fourteen cogenetic quartz-biotite pairs from gneissic wall rocks, and 22 quartz, 16 calcite, and 8 biotite samples and 1 sample of albite from fissure-filling veins in the Western Tauern Window were analyzed for their oxygen isotope composition. The δ18O values show the following ranges: (a) quartz, +6.0 in fissure in amphibolite to +10.3 in fissures in granite gneisses; (b) biotite, +2.5 to +6.7; and (c) calcite, +7.0 to +8.9. The δ18O value of albite is +7.1. Only a small variation in the hydrogen isotope composition of biotite was detected. δD values of 7 biotites from gneisses and fissure fillings varied from −54 to −59. There is no significant difference in the hydrogen isotope composition of fissure biotite and biotite from the host rock. This indicates that a common water source of probably deep-seated origin existed, with no detectable contribution from isotopically light meteoric water. Oxygen isotope fractionations between coexisting quartz and biotite of 3.5 to 7.0‰ indicate equilibrium temperatures of 640 ° to 450 ° C, respectively, using the fractionation curve of Hoernes and Friedrichsen (1978). The highest temperatures of equilibration are for the rocks at the Alpenhauptkamm, i.e., the central part of the Tauern Window. Successively lower temperatures are found to the north and to the south of the Alpenhauptkamm along a traverse through Penninic units of the Tauern Window. The metamorphism of the host rocks and the filling of fissures has occurred at the same temperature in a given sample locality.  相似文献   

20.
The Hokko prospect is located in the Minamikayabe area southwestern Hokkaido, Japan, where gold-bearing quartz veins of Pliocene age are exposed at the surface. The alteration mineral assemblage is typical of low-sulfidation epithermal systems, with the quartz veins associated with adularia alteration overprinted on Late Miocene propylitic alteration. Fluid inclusion studies of the vein quartz reveal mean homogenization temperatures of approximately 220 °C, and the co-existence of low-salinity (<2 wt.% NaCl equivalent) and moderate salinity (2 to 12 wt.% NaCl equivalent) fluid inclusions within the same veins. The moderate salinity fluid inclusions (2–12 wt.% NaCl equivalent) typically have relatively low homogenization temperatures between 150° to 200 °C. The results obtained from stable isotope analysis of  δ18O in quartz vein material showed a gradual decrease in  δ18O signatures with increasing depth. The majority of the samples have calculated fluid source signatures (δ18OH2O) between −8.0 and −10.0‰, but there is a significant change in the composition above 185 m drill depth. The shallower samples in particular show a wide range of oxygen isotope signatures that are associated with the moderate salinity fluid inclusions. We interpret that low-salinity inclusions within the Hokko system represent the composition of the liquid phase of the fluid, before boiling, and that the moderate-salinity inclusions are representative of the residual liquid phase, after extensive non-adiabatic boiling and vapor loss in an open system. This mechanism resulted in the entrapment of fluids with variable salinities at the same time, and in close proximity to each other. This is also reflected in the  δ18OH2O values which become more variable and heavier where the moderate-salinity inclusions occur. Deposition of ore minerals within the Hokko vein system also occurred at this time as a result of boiling and gas loss. Received: 30 May 1997 / Accepted: 6 January 1998  相似文献   

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