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1.
The Orlica-Snieznik and Jeseník Mountains correspond to three main domes from west to east: the Snieznik, Keprnfk and Desna domes. They are composed of a basement of autochthonous gneisses, a thick series of blastomylonites and a supposed para-autochthonous or allochthonous metamorphic pre-Devonian to Devonian cover. Their broad direction is NNE-SSW. 40Ar-39Ar radiometric measurements allow three main groups of ages to be defined. (1) 300–310 Ma, represented in the Keprník and Desná domes. This age is interpretated following the constraints on the age of the metamorphism, which is linked with the extensional process occurring during the Westphalian. (2) 320–340 Ma, represented mainly in the Snieznik Dome, but not in the Keprnfk Massif. The nappe structure of Orlik-Vysoká hole, in the northern area of the Desna Dome, also exhibits this age, which is interpretated as reflecting the period of the major Variscan Barrowian metamorphism, which accompanied the compressional process. It is only represented in the zones where the extensional process was not strong enough to result in a complete overprinting. (3) 340–440 Ma, corresponding to a very strictly defined area in the eastern rim of the Desná Dome occupied by ultramylonites and mylonites. These ages, obtained on muscovites, result from an incomplete resetting of the minerals developed during the cooling of a granitic protolith and mylonitized during the extensional process. A laser probe analysis confirms the extreme inhomogeneity of the ages of the muscovites and their different resetting from one grain to another. The Late Alpine overprinting is more discrete, but can be deciphered through the low extraction temperatures with ages between 80 and 120 Ma. These ages can be compared with Alpine ages in the close Western Carpathians.  相似文献   

2.
The influence of alkaline aqueous solutions on the properties of bentonite was investigated to evaluate the performance of bentonitic engineered barriers when contacted with alkaline groundwater. Batch and hydraulic conductivity tests were conducted on Na-bentonite using six different alkaline aqueous solutions. For the batch tests, almost no change in the montmorillonite fraction of the bentonite was observed after reacting with alkaline solutions (pH = 8.4–13.1), regardless of the solution type. On the other hand, aluminosilicate minerals (e.g., albite) were dissolved and secondary minerals (e.g., anorthite) were formed in alkaline NaOH solutions (pH > 13). The cation (Ca or Na) concentration primarily affected the swelling properties of bentonite rather than the pH of the solution, which was comparable to the results of the hydraulic conductivity tests. For the Ca solutions, the hydraulic conductivity of the bentonite specimen to the 0.02 mol/L Ca(OH)2 solution (6.5 × 10?9 cm/s) was approximately an order of magnitude lower than that of the bentonite specimen to the 0.02 mol/L Ca(OH)2 + 1 mol/L CaCl2 solution (5.0 × 10?8 cm/s), whereas the hydraulic conductivity to the 0.02 mol/L Ca(OH)2 + 1 mol/L CaCl2 solution (pH = 11.3) (5.0 × 10?8 cm/s) was slightly higher than that to the 1 mol/L CaCl2 solution (pHi = 8.4) (4.4 × 10?8 cm/s). For the NaOH solutions with pH > 13, the hydraulic conductivity of the bentonite specimen decreased with increasing Na concentration, suggesting that the effect of Na concentration was more dominant than that of permeant pH.  相似文献   

3.
We have used correlative analysis between mean December-January-February winter wind velocities, measured at the Xisha Meteorological Observatory (16°50′N, 112°20′E) in the middle of the South China Sea, and mean δ18O data for the corresponding month from Porites lutea coral, collected in Longwan waters (19°20′N, 110°39′E), to obtain a linear equation relating the two datasets. This winter wind velocity for the South China Sea (WMIIscs) can then be correlated to the coral δ18O by the equation WMIIscs = −1.213-1.351 δ18O (‰ PDB), r = −0.60, n = 40, P = 0.01. From this, the calculated WMIIscs-δ18O series from 1944 to 1997 tends to decrease during the 1940s to the 1960s; it increases slightly during the 1970s and then decreases again in the 1980s and 1990s. The calculated decadal mean WMIIscs-δ18O series had a obvious decrease from 5.92 to 4.63 m/s during the period of 1944-1997. The calculated yearly mean WMIIscs-δ18O value is 5.58 m/s from 1944 to 1976 and this decreases to 4.85 m/s from 1977 to 1998. That is the opposite trend to the observed yearly mean SST variation. The yearly mean SST anomaly is −0.27° from 1943 to 1976 and this increases to +0.16° from 1977 to 1998. Spectral analysis used on a 54-year-long calculated WMIIscs-δ18O series produces spectral peaks at 2.4-7 yr, which can be closely correlated with the quasibiennial oscillation band (QBO band, 2-2.4 yr) and the El Ñino southern oscillation band (ENSO band, 3-8 yr). Hence most of the variability of the winter monsoon intensity in the middle of the South China Sea is mainly constrained by changes in the thermal difference between the land and the adjoining sea area, perhaps due to global warming.  相似文献   

4.
Isotopic and chemical composition of groundwater from wells and springs, and surface water from the basalt-dominated Axum area (northern Ethiopia) provides evidence for the origin of water and dissolved species. Shallow (depth < 40 m) and deep groundwater are distinguished by both chemical and isotopic composition. Deep groundwater is significantly enriched in dissolved inorganic carbon up to 40 mmol l−1 and in concentrations of Ca2+, Mg2+, Na+ and Si(OH)4 compared to the shallow type.The δ2H and δ18O values of all solutions clearly indicate meteoric origin. Shifts from the local meteoric water line are attributed to evaporation of surface and spring water, and to strong water–rock interaction. The δ13CDIC values of shallow groundwater between −12 and −7‰ (VPDB) display the uptake of CO2 from local soil horizons, whereas δ13CDIC of deep groundwater ranges from −5 to +1‰. Considering open system conditions with respect to gaseous CO2, δ13CDIC = +1‰ of the deep groundwater with highest PCO2 = 10−0.9 atm yields δ13CCO2(gas) ≈ −5‰, which is close to the stable carbon isotopic composition of magmatic CO2. Accordingly, stable carbon isotope ratios within the above range are referred to individual proportions of CO2 from soil and magmatic origin. The uptake of magmatic CO2 results in elevated cations and Si(OH)4 concentrations. Weathering of local basalts is documented by 87Sr/86Sr ratios of the groundwater from 0.7038 to 0.7059. Highest values indicate Sr release from the basement rocks. Besides weathering of silicates, neoformation of solids has to be considered, which results in the formation of, e.g., kaolinite and montmorillonite. In several solutions supersaturation with respect to calcite is reached by outgassing of CO2 from the solution leading to secondary calcite formation.  相似文献   

5.
The local and geometrical structure around gold (III) e.g., Au3+ ions in aqueous solution with different OH−/Cl− molar ratios, has been investigated by X-ray absorption spectroscopy (XAS). X-ray absorption near-edge structure (XANES) spectra of [AuCln(OH)4−n]− solutions have been calculated and the multiple-scattering spectral features have been attributed to Cl d-states, axial water molecules and the replacement of Cl− ligands by OH− ligands. A square–planar geometry for [AuCln(OH)4−n]− with two axial water molecules has been identified. Moreover, a spectral correlation between XANES features and the type of planar atoms has been identified. By extended X-ray absorption fine structure spectra (EXAFS), the planar Au bond distances in the solutions have also been determined, e.g., 2.28 Å for Au–Cl and 1.98 Å for Au–O, respectively. The same EXAFS analysis provides evidence that the peak at about 4.0 Å in solutions with the lowest OH−/Cl− molar ratio arises from collinear Cl–Au–Cl multiple-scattering contributions. For the first time, a complete detailed reconstruction of the hydration structure of an Au ion at different pH values has been achieved.  相似文献   

6.
The mordenite ore deposit of Los Escullos has a surface area of 106 m2 with an average thickness of 5 m and estimated reserves of 7,500,000 tons of mordenite–bentonite. It is made up of horizontal layers of interbedded epiclastic tuffs with volcanic bentonitised materials which have been subjected to hydromagmatic activity. The layers are essentially composed of bentonite and mordenite with lesser amounts of quartz, cristobalite, biotite, plagioclase, chlorite, amphiboles, titanomagnetite, ilmenite and calcite. The harder layers display a higher proportion of plagioclase crystals and are enriched in Al2O3, CaO, Fe2O3, TiO2, P2O5, Cu, Zn, Co, Cr, Ni and V, while the more altered layers contain larger contents of SiO2, K2O and Y. The amount of sodium increases (from 2% to 4%) relative to depth. Alteration processes resulted in a reduction in the contents of CaO, K2O and MnO and increase in Na2O and MgO. The beds of volcanic ash-tuffs have been devitrified by hydrothermal solutions giving rise to bentonites and sodium- and silica-rich residual fluids which have partly crystallized as mordenite and cristobalite. The raw material (mordenite–bentonite) can be improved removing biotite (magnetic separation) and plagioclase and quartz (by floating methods); however, the mordenite–bentonite mineral assemblage is practically impossible to separate due to the size of the crystals (average 0.5 μm under SEM–EDAX). In turn, this upgraded raw material has very useful properties (total area=520 m2/g and cation exchange capacity=70 meq/100 g) which may make it suitable for use in absorption processes (e.g. deodorization, cationic exchange), catalysis and molecular sieving.  相似文献   

7.
A revised regular solution-type thermodynamic model for twelve-component silicate liquids in the system SiO2-TiO2-Al2O3-Fe2O3-Cr2O3-FeO-MgO-CaO-Na2O-K2O-P2O5-H2O is calibrated. The model is referenced to previously published standard state thermodynamic properties and is derived from a set of internally consistent thermodynamic models for solid solutions of the igneous rock forming minerals, including: (Mg,Fe2+,Ca)-olivines, (Na,Mg,Fe2+,Ca)M2 (Mg,Fe2+, Ti, Fe3+, Al)M1 (Fe3+, Al,Si)2 TETO6-pyroxenes, (Na,Ca,K)-feldspars, (Mg,Fe2+) (Fe3+, Al, Cr)2O4-(Mg,Fe2+)2 TiO4 spinels and (Fe2+, Mg, Mn2+)TiO3-Fe2O3 rhombohedral oxides. The calibration utilizes over 2,500 experimentally determined compositions of silicate liquids coexisting at known temperatures, pressures and oxygen fugacities with apatite ±feldspar ±leucite ±olivine ±pyroxene ±quartz ±rhombohedral oxides ±spinel ±whitlockite ±water. The model is applicable to natural magmatic compositions (both hydrous and anhydrous), ranging from potash ankaratrites to rhyolites, over the temperature (T) range 900°–1700°C and pressures (P) up to 4 GPa. The model is implemented as a software package (MELTS) which may be used to simulate igneous processes such as (1) equilibrium or fractional crystallization, (2) isothermal, isenthalpic or isochoric assimilation, and (3) degassing of volatiles. Phase equilibria are predicted using the MELTS package by specifying bulk composition of the system and either (1) T and P, (2) enthalpy (H) and P, (3) entropy (S) and P, or (4) T and volume (V). Phase relations in systems open to oxygen are determined by directly specifying the f o 2 or the T-P-f o 2 (or equivalently H-P-f o 2, S-P-f o 2, T-V-f o 2) evolution path. Calculations are performed by constrained minimization of the appropriate thermodynamic potential. Compositions and proportions of solids and liquids in the equilibrium assemblage are computed.  相似文献   

8.
 H2O activities in concentrated NaCl solutions were measured in the ranges 600°–900° C and 2–15 kbar and at NaCl concentrations up to halite saturation by depression of the brucite (Mg(OH)2) – periclase (MgO) dehydration equilibrium. Experiments were made in internally heated Ar pressure apparatus at 2 and 4.2 kbar and in 1.91-cm-diameter piston-cylinder apparatus with NaCl pressure medium at 4.2, 7, 10 and 15 kbar. Fluid compositions in equilibrium with brucite and periclase were reversed to closures of less than 2 mol% by measuring weight changes after drying of punctured Pt capsules. Brucite-periclase equilibrium in the binary system was redetermined using coarsely crystalline synthetic brucite and periclase to inhibit back-reaction in quenching. These data lead to a linear expression for the standard Gibbs free energy of the brucite dehydration reaction in the experimental temperature range: ΔG° (±120J)=73418–134.95T(K). Using this function as a baseline, the experimental dehydration points in the system MgO−H2O−NaCl lead to a simple systematic relationship of high-temperature H2O activity in NaCl solution. At low pressure and low fluid densities near 2 kbar the H2O activity is closely approximated by its mole fraction. At pressures of 10 kbar and greater, with fluid densities approaching those of condensed H2O, the H2O activity becomes nearly equal to the square of its mole fraction. Isobaric halite saturation points terminating the univariant brucite-periclase curves were determined at each experimental pressure. The five temperature-composition points in the system NaCl−H2O are in close agreement with the halite saturation curves (liquidus curves) given by existing data from differential thermal analysis to 6 kbar. Solubility of MgO in the vapor phase near halite saturation is much less than one mole percent and could not have influenced our determinations. Activity concentration relations in the experimental P-T range may be retrieved for the binary system H2O-NaCl from our brucite-periclase data and from halite liquidus data with minor extrapolation. At two kbar, solutions closely approach an ideal gas mixture, whereas at 10 kbar and above the solutions closely approximate an ideal fused salt mixture, where the activities of H2O and NaCl correspond to an ideal activity formulation. This profound pressure-induced change of state may be characterized by the activity (a) – concentration (X) expression: a H 2O=X H 2O/(1+αX NaCl), and a NaCl=(1+α)(1+α)[X NaCl/(1+αX NaCl)](1+α). The parameter α is determined by regression of the brucite-periclase H2O activity data: α=exp[A–B/ϱH 2O ]-CP/T, where A=4.226, B=2.9605, C=164.984, and P is in kbar, T is in Kelvins, and ϱH 2O is the density of H2O at given P and T in g/cm3. These formulas reproduce both the H2O activity data and the NaCl activity data with a standard deviation of ±0.010. The thermodynamic behavior of concentrated NaCl solutions at high temperature and pressure is thus much simpler than portrayed by extended Debye-Hückel theory. The low H2O activity at high pressures in concentrated supercritical NaCl solutions (or hydrosaline melts) indicates that such solutions should be feasible as chemically active fluids capable of coexisting with solid rocks and silicate liquids (and a CO2-rich vapor) in many processes of deep crustal and upper mantle metamorphism and metasomatism. Received: 1 September 1995 / Accepted: 24 March 1996  相似文献   

9.
The synthetic amphibole Na0.95(Li0.95Mg1.05)Mg5Si8O22(OH)2 was studied in situ at high-T, using IR OH-stretching spectroscopy and synchrotron X-ray powder diffraction. At room-T the sample has P21 /m symmetry, as shown by the FTIR spectrum. It shows in the OH region two well-defined and intense absorptions at 3,748 and 3,712 cm−1, respectively, and two minor bands at 3,667 and 3,687 cm−1. The main bands are assigned to the two independent O–H groups in the primitive structure. The two minor bands evidencing the presence of small amount of vacant A-site (A□0.05). With increasing T, these bands shift continuously and merge into a unique absorption at high temperature. A change as a function of increasing T is revealed by the evolution of the refined unit-cell parameters, whose trend shows a transition to C2/m at about 320–330°C. The spontaneous scalar strain, fitted with a tricritical 2–6 Landau potential, gives a T c of 325(10)°C (β parameter = 0.27). Comparison with the second-order P21 /m ⇔ C2/m phase transition at 255°C for synthetic amphibole ANa0.8B(Na0.8Mg1.2)CMg5Si8O22(OH)2 indicates that the substitution of Na with Li at the B-sites strongly affects the thermodynamic character and the T c of the phase transition. The comparison of LNMSH amphiboles with cummingtonitic ones shows that the high-T thermodynamic behaviour is affected by A-site occupancy.  相似文献   

10.
The Amassia–Stepanavan blueschist-ophiolite complex of the Lesser Caucasus in NW Armenia is part of an Upper Cretaceous-Cenozoic belt, which presents similar metamorphic features as other suture zones from Turkey to Iran. The blueschists include calcschists, metaconglomerates, quartzites, gneisses and metabasites, suggesting a tectonic mélange within an accretionary prism. This blueschist mélange is tectonically overlain by a low-metamorphic grade ophiolite sequence composed of serpentinites, gabbro-norite pods, plagiogranites, basalts and radiolarites. The metabasites include high-P assemblages (glaucophane–aegirine–clinozoisite–phengite), which indicate maximal burial pressure of ∼1.2 GPa at ∼550°C. Most blueschists show evidence of greenschist retrogression (chlorite—epidote, actinolite), but locally epidote-amphibolite conditions were attained (garnet—epidote, Ca/Na amphibole) at a pressure of ∼0.6 GPa and a temperature of ∼500°C. This LP–MT retrogression is coeval with exhumation and nappe-stacking of lower grade units over higher grade ones. 40Ar/39Ar phengite ages obtained on the high-P assemblages range between 95 and 90 Ma, while ages obtained for epidote-amphibolite retrogression assemblages range within 73.5–71 Ma. These two metamorphic phases are significant of (1) HP metamorphism during a phase of subduction in the Cenomanian–Turonian times followed by (2) exhumation in the greenschist to epidote-amphibolite facies conditions during the Upper Campanian/Maastrichtian due to the onset of continental subduction of the South Armenian block below Eurasia.  相似文献   

11.
Frequent sampling during an annual cycle of dissolved(<0.45 m) and suspended (>0.45 m) elementshas been conducted in the Kafue River at Raglan'sFarm, upstream from the mining activities within theCopperbelt Province, Zambia. Additional sampling ofsediment and interstitial pore water was conductedduring low water discharge. The presence of carbonateswithin the drainage basin naturally gives rise to highelement concentrations in the dissolved phase(Ca = 626, Mg = 494, Na = 360 and K = 24 mmol l-1).During the rainy season the relative composition ofthe dissolved elements indicated a wash out ofaccumulated weathering products and mineralisedorganic material from the unsaturated zone of the soilprofile. High concentrations of dissolved Al, Fe andMn were measured during high water discharge. At lowwater discharge the sediment was a major source of Fe,Mn and associated Co and Cu to the water column.Enhanced concentrations of dissolved and suspended S,Co and Cu during the rainy season indicated thatatmospheric deposited particles from the mining areawere washed out into the river. Autochthonousformation of particles rich in Si indicated diatomproduction during low water discharge.  相似文献   

12.
Abstract Explosive volcanic activity is recorded in the Upper Jurassic of the Paris Basin and the Subalpine Basin of France by the identification of five bentonite horizons. These layers occur in Lower Oxfordian (cordatum ammonite zone) to Middle Oxfordian (plicatilis zone) clays and silty clays deposited in outer platform environments. In the Paris Basin, a thick bentonite (10–15 cm), identified in boreholes and in outcrop, is dominated by dioctahedral smectite (95%) with trace amounts of kaolinite, illite and chlorite. In contrast, five bentonites identified in the Subalpine Basin, where burial diagenesis and fluid circulation were more important, are composed of a mixture of kaolinite and regular or random illite/smectite mixed-layer clays in variable proportions, indicating a K-bentonite. In the Subalpine Basin, a 2–15 cm thick bentonite underlain by a layer affected by sulphate–carbonate mineralization can be correlated over 2000 km2. Euhedral zircon, apatite and biotite crystals have been identified in all the bentonites. The geochemical composition of the bentonites in both basins is characterized by high concentrations of Hf, Nb, Pb, Ta, Th, Ti, U, Y, Zr and low concentrations of Cr, Cs and Rb. Biostratigraphical and geochemical data suggest that the thick bentonite in the Paris Basin correlates with the thickest bentonite in the Subalpine Basin, located 400 km to the south. These horizons indicate that significant explosive volcanic events occurred during the Middle Oxfordian and provide potential long-distance isochronous marker beds. Immobile element discrimination diagrams and rare-earth element characteristics indicate that the original ash compositions of the thickest bentonites correspond to a trachyandesitic source from a within-plate alkaline series that was probably related to North Atlantic rifting.  相似文献   

13.
Summary This study reports foggite and churchite-(Y) from two spatially separate locations in the guano-related phosphate deposit from the Cioclovina Cave, Romania. Optical microscope observations, powder X-ray diffraction, electron microprobe analyses, and FTIR were used in the analysis of the two minerals. The chemical composition of foggite was determined to be Ca0.925(Al0.91Fe2+0.016)Σ0.926(P0.991Si0.043)Σ1.034O3.74(OH)2.26 · H2O and churchite-(Y) [(Y0.830Dy0.043Er0.033Gd0.029Yb0.022)Σ0.957Ca0.009]P1.023O4.00 · 2H2O. Chemical analyses of Cioclovina churchite-(Y) clearly revealed enrichment in lanthanides of even atomic number. The refined unit-cell parameters are for foggite (orthorhombic) a = 9.264(1) ?, b = 21.334(8) ?, c = 5.197(7) ?, and V = 1027.13(8) ?3 (Z = 8); for churchite-(Y) (monoclinic): a = 5.578(8) ?, b = 15.013(6) ?, c = 6.277(8) ?, β = 117.94(4)°, and V = 464.38(5) ?3 (Z = 4). FTIR spectrum of churchite-(Y) exhibits all the bands assigned to the vibrations of PO4, OH, and water groups. Unlike other documented occurrences of foggite and churchite-(Y), in Cioclovina Cave, the occurrence of these minerals are related to a process that phosphatized subjacent limestone and various cave sediments (sand, clay, and limy mud) to form a complex phosphate assemblage. The minerals are presumably derived from phosphate-rich solutions that reacted with clay earth while moving downward through the sediments. Foggite was formed at the expense of the originally precipitated crandallite. Locally concentrated yttrium, REE, and dissolved phosphate are probably responsible for the precipitation of churchite-(Y). Present address: Department of Geology, University of South Florida, Tampa, FL, USA  相似文献   

14.
Ca-type bentonite deposits of economic interest occur associated with rhyolitic rocks in the Lebombo volcanics. From previous geological studies on the deposits, besides the economic aspects, little is known about the main formation mechanism of beds of bentonite that can be more than 15 m thick, in some places. Chemical analyses of bentonite samples indicate that elements such as Ca, Mg, Sr, Zn, Cu and Sc are markedly enriched in bentonite in comparison to the parent rock. Other elements such as K, Na, Rb and Ba are depleted in bentonite. HREE (Yb, Lu) and Y are depleted in the bentonite samples, as well as Cs, Rb, Ta, U, Ba, Co, Cr and Pb. Concentrations of the LREE (La, Ce, Nd, Sm, Eu), Sc and Ga are slightly higher in the bentonites than in the parent rocks. The chondrite-normalized REE patterns show identical trends both in the rhyolites and bentonites samples. Alteration of the parent rocks to bentonite is associated with leaching and subsequent removal of, principally, K and Na in open-system conditions.  相似文献   

15.
Pyrope-knorringite garnets, Mg3(Al1-X Cr3+X)2Si3O12 with X=0.25, 0.50, and 1.00, were synthesized between 9 and 16 GPa and 1300 and 1600 °C, using multianvil high-pressure techniques. The garnets with X=0.25 and 0.50 are fine-grained, pink and violet in color. The end-member knorringites with X=1.00 are black when compact and gray when coarse-grained. The fine powder is greenish gray in natural light and pale pink under a tungsten lamp. Powder remission spectra in the wavenumber range 30 000–10 000 cm–1 on finely powdered crystals were measured by two different methods: (I.) by the use of a small integrating sphere for small samples or (II.) microscope-spectrometric measurement using diffusely reflected radiation from a 45° illuminated microsample. Both methods yielded similar diffuse reflectance spectra. The following crystal-field parameters of [6]Cr3+ were determined for garnets with X=0.25, 0.50, 1.00: 10 Dq=17 856, 17 596, 17 286 cm–1; and B=654, 677, 706 cm–1; nephelauxetic ratio =(Bfield/Bfree)= 0.71, 0.74, 0.77. The -values indicate decreasing covalency of the Cr–O bond with increasing Cr content. The 10 Dq value for together with the mean Cr–O distance in end-member knorringite, 1.96 Å (Novak and Gibbs 1971), were used to calculate from the spectral data, local mean Cr–O distances (Langer 2001a) as a function of composition. The results indicate relatively strong local site relaxation with a value of =0.77.  相似文献   

16.
The western terranes exposed east of the Pan-African suture in western Hoggar (southwest Algeria), are reexamined in the light of new structural, petrologic and by the 40Ar/39Ar laser probe data on metamorphic micas and amphiboles. To the north, the Tassendjanet nappe includes the Paleoproterozoic basement, its Mesoproterozoic cover and mafic rocks representing the roots of a ca. 680 Ma arc overlain by Late Neoproterozoic andesites and volcanic greywackes. The nappe preserved at rather shallow crustal level in the east was emplaced southward (D1a) to southeastward (D2). In the south, two metamorphic suites are distinguished. The Tideridjaouine–Tileouine high-pressure metamorphic belt (T=550–600 °C, P=1.4–1.8 GPa) represents a slab of subducted continental material exposed along the western edge of the In Ouzzal granulite unit interpreted as a microcontinent. Differential exhumation of tectonic slices from the high-pressure belt occurred around 615–600 Ma through a system of west-directed recumbent folds (D1b). The Egatalis high grade belt in the west was intruded by syn-metamorphic gabbro–norite bodies. It includes unretrogressed low-pressure granulite facies rocks (T around 750–800 °C, P0.45 GPa) cooled at a rate of 15°/m.y. between 600 and 580 Ma, and followed by the emplacement of several late-kinematic granitic plutons. Final exhumation of the low-pressure, high-temperature metamorphic rocks, that are not found as pebbles in the molasse, took place in the Late Cambrian. The early and relatively fast cooling of the high-pressure and high-temperature metamorphic rocks of the southern part of the Tassendjanet terrane is at variance with the slow cooling of central Hoggar where repeated magmatic activity as young as Late Cambrian occurred [Lithos 45 (1998) 245].  相似文献   

17.
The behaviour of the ammonium ion in synthetic buddingtonite, N(D,H)4AlSi3O8, has been studied by infrared (IR) spectroscopy from 20 K to 298 K and by 2H NMR spectroscopy from 120 K to 298 K. IR spectra were collected from 500 to 3500 cm–1. Static 2H NMR spectra collected at 298 K and 120 K are very similar, consisting of a single sharp isotropic resonance, indicating complete averaging of quadrupolar interactions and implying that at these temperatures the ammonium ion is in rapid (<1 s) randomised motion within the M-site cavity of the feldspar framework. NMR spectroscopy indicates that the splitting of the internal modes of the ammonium ion observed by IR spectroscopy is not due to freezing in of the ammonium ion. This observation rules out the formation of a preferred N–H...O hydrogen bond, with precession of the ion about it, as proposed by Kimball and Megaw (1978), because any N–H...O hydrogen bond must be very weak and transient in nature. Contraction of the cavity site upon cooling imposes a distortion upon the ammonium ion that affects vibrational modes. This distortion does not affect the motion of the ammonium ion as observed on the NMR time-scale.  相似文献   

18.
H2O activities in supercritical fluids in the system KCl-H2O-(MgO) were measured at pressures of 1, 2, 4, 7, 10 and 15  kbar by numerous reversals of vapor compositions in equilibrium with brucite and periclase. Measurements spanned the range 550–900 °C. A change of state of solute KCl occurs as pressures increase above 2 kbar, by which H2O activity becomes very low and, at pressures of 4 kbar and above, nearly coincident with the square of the mole fraction (x H2O). The effect undoubtedly results primarily from ionic dissociation as H2O density (ρH2O) approaches 1 gm/cm3, and is more pronounced than in the NaCl-H2O system at the same P-T-X conditions. Six values of solute KCl activity were yielded by terminal points of the isobaric brucite-periclase T-x H2O curves where sylvite saturation occurs. The H2O mole fraction of the isobaric invariant assemblage brucite-periclase-sylvite-fluid is near 0.52 at all pressures, and the corresponding temperatures span only 100 °C between 1 and 15 kbar. This remarkable convergence of the isobaric equilibrium curves reflects the great influence of pressure on lowering of both KCl and H2O activities. The H2O and KCl activities can be expressed by the formulas: a H2O = γH2O[x H2O+(1 + (1 + α)x KCl)], and a KCL = γKCl[(1 + α)x KCl/(x H2O +(1 + α)x KCl)](1 + α), where α is a degree of dissociation parameter which increases from zero at the lowest pressures to near one at high pressures and the γ's are activity coefficients based on an empirical regular solution parameter W: ln γi = (1 − xi)2W. Least squares fitting of our H2O and KCl activity data evaluates the parameters: α = exp(4.166 −2.709/ρH2O) − 212.1P/T, and W = (−589.6 − 23.10P) /T, with ρH2O in gm/cm3, P in kbar and T in K. The standard deviation from the measured activities is only ± 0.014. The equations define isobaric liquidus curves, which are in perfect agreement with previous DTA liquidus measurements at 0.5–2 kbar, but which depart progressively from their extrapolation to higher pressures because of the pressure-induced dissociation effect. The great similarity of the NaCl-H2O and KCl-H2O systems suggests that H2O activities in the ternary NaCl-KCl-H2O system can be described with reasonable accuracy by assuming proportionality between the binary systems. This assumption was verified by a few reconnaissance measurements at 10 kbar of the brucite-periclase equilibrium with a Na/(Na + K) ratio of 0.5 and of the saturation temperature for Na/(Na + K) of 0.35 and 0.50. At that pressure the brucite-periclase curves reach a lowest x H2O of 0.45 and a temperature of 587 °C before salt saturation occurs, values considerably lower than in either binary. This double-salt eutectic effect may have a significant application to natural polyionic hypersaline solutions in the deep crust and upper mantle in that higher solute concentrations and very low H2O activities may be realized in complex solutions before salt saturation occurs. Concentrated salt solutions seem, from this standpoint, and also because of high mechanical mobility and alkali-exchanging potential, feasible as metasomatic fluids for a variety of deep-crust and upper mantle processes. Received: 9 August 1996 / Accepted: 15 November 1996  相似文献   

19.
Zusammenfassung Emmonsit kristallisiert triklin, RaumgruppeP , Gitterkonstanten:a 0=7,90 Å,b 0=8,00 Å,c 0=7,62 Å, =96o44, =95o 0, =84o 28,Z=2. Der Strukturtyp wurde aus 3-dimensionalen photographischen Röntgendaten ermittelt. Die Eisenatome werden je von 6 Sauerstoffen verzerrt oktaedrisch koordiniert. Jedes Telluratom wird von 3 Sauerstoffen in einem Abstand <2,0 Å umgeben. Ein vierter Sauerstoff hat bezüglich dieser drei einen um etwa 25–35% größeren Abstand, so daß jedes Telluratom im weiteren Sinne eine (3+1)-Koordination aufweist.
The structure type of emmonsite, {Fe2[TeO3]3·H2O}·xxH2O (x=0–1)
Summary Emmonsite is triclinic with space groupP , and lattice constantsa 0=7.90 Å,b 0=8.00 Å,c 0=7.62 Å, =96o 44, =95o 0, =840 28,Z=2. The structure type is derived from 3-dimensional photographic X-ray data. The iron atoms are coordinated by six oxygens in the form of a distorted octahedron. Each tellurium atom is coordinated to 3 oxygens at a distance <2.0 Å. Compared with these 3 Te–O distance the distance of a fourth oxygen is only 25 to 35% greater; therefore each tellurium atom has a (3+1)-coordination of oxygens.

Mit 2 Abbildungen  相似文献   

20.
We measured both mass-dependent isotope fractionation of δ88Sr (88Sr/86Sr) and radiogenic isotopic variation of Sr (87Sr/86Sr) for the Neoproterozoic Doushantuo Formation that deposited as a cap carbonate immediately above the Marinoan-related Nantuo Tillite. The δ88Sr and 87Sr/86Sr compositions showed three remarkable characteristics: (1) high radiogenic 87Sr/86Sr values and gradual decrease in the 87Sr/86Sr ratios, (2) anomalously low δ88Sr values at the lower part cap carbonate, and (3) a clear correlation between 87Sr/86Sr and δ88Sr values. These isotopic signatures can be explained by assuming an extreme greenhouse condition after the Marinoan glaciation. Surface seawater, mixed with a large amount of freshwater from continental crusts with high 87Sr/86Sr and lighter δ88Sr ratios, was formed during the extreme global warming after the glacial event. High atmospheric CO2 content caused sudden precipitation of cap carbonate from the surface seawater with high 87Sr/86Sr and lighter δ88Sr ratios. Subsequently, the mixing of the underlying seawater, with unradiogenic Sr isotope compositions and normal δ88Sr ratios, probably caused gradual decrease of the 87Sr/86Sr ratios of the seawater and deposition of carbonate with normal δ88Sr ratios. The combination of 87Sr/86Sr and δ88Sr isotope systematics gives us new insights on the surface evolution after the Snowball Earth.  相似文献   

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