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1.
Zusammenfassung Der Pleochroismus der OH-Streckfrequenz (=3,16 ±0,02 ) zeigt sowohl für -Zoisit als auch für -Zoisit, daß die OH-Dipole paralel [001] orientiert sind.
Measurement of the infrared-pleochroism in minerals. X. The pleochroism of the OH-stretching frequency in zoisite
Summary The pleochroism of the OH-stretching frequency (=3.16 ±0.02 ) proves for - and -zoisite that the OH-dipoles are oriented parallel [001].

Mit 1 Abbildung  相似文献   

2.
Mean and turbulent velocity measurements of supersonic mixing layers   总被引：1，自引：0，他引：1  
The behavior of supersonic mixing layers under three conditions has been examined by schlieren photography and laser Doppler velocimetry. In the schlieren photographs, some largescale, repetitive patterns were observed within the mixing layer; however, these structures do not appear to dominate the mixing layer character under the present flow conditions. It was found that higher levels of secondary freestream turbulence did not increase the peak turbulence intensity observed within the mixing layer, but slightly increased the growth rate. Higher levels of freestream turbulence also reduced the axial distance required for development of the mean velocity. At higher convective Mach numbers, the mixing layer growth rate was found to be smaller than that of an incompressible mixing layer at the same velocity and freestream density ratio. The increase in convective Mach number also caused a decrease in the turbulence intensity ( u /U).List of Symbols a speed of sound - b total mixing layer thickness betweenU 1 – 0.1U andU 2 + 0.1U - f normalized third moment ofu-velocity,f u 3/(U)3 - g normalized triple product ofu 2 v,g u 2 v/(U)3 - h normalized triple product ofu v 2, h uv' 2/(U)3 - l u axial distance for similarity in the mean velocity - l u axial distance for similarity in the turbulence intensity - M Mach number - M c convective Mach number (for 1=2),M c (U 1–U 2)/(a 1+a 2) - P static pressure - r freestream velocity ratio,rU 2/U 1 - Re unit Reynolds number,Re U/ - s freestream density ratio,s 2/ 1 - T t total temperature - u instantaneous streamwise velocity - u deviation ofu-velocity,u u–U - U local mean streamwise velocity - U 1 primary freestream velocity - U 2 secondary freestream velocity - U average of freestream velocities, ¯U (U 1 +U 2)/2 - U freestream velocity difference,U U 1 –U 2 - v instantaneous transverse velocity - v deviation ofv-velocity,v v – V - V local mean transverse velocity - x streamwise coordinate - y transverse coordinate - y 0 transverse location of the mixing layer centerline - ensemble average - ratio of specific heats - boundary layer thickness (y-location at 99.5% of free-stream velocity) - similarity coordinate, (y –y 0)/b - compressible boundary layer momentum thickness - viscosity - density - standard deviation - dimensionless velocity, (U –U 2)/U - 1 primary stream - 2 secondary stream A version of this paper was presented at the 11th Symposium on Turbulence, October 17–19, 1988, University of Missouri-Rolla  相似文献   

3.
Metasomatic columns hosted in dolomitic marbles in the thermal aureole of the Traversella monzodiorite (Ivrea, Italy) differ by their mineralogy and/or mineral composition. Three groups have been distinguished. In group A, the first zone always contains forsterite-calcite and the second zone contains clinopyroxene. The last zone is made of wollastonite (A1), andradite-rich garnet (A 2) or grossular-rich garnet (A 3). In group B, tremolite instead of forsterite occurs in the first two zones. In group C columns, there are only two zones and clinohumite or chondrodite characterize the first zone.Field, petrographic and chemical data demonstrate that the occurrence of contrasted mineral zonations in the same protolith has not been induced by local heterogeneities in the dolomitic marbles. The presence of tremolite in group B instead of forsterite is due to the lower temperature prevailing in the external part of the contact aureole. Chemical data as well as - diagrams suggest that the columns in groups A and C were formed through the interaction of the dolomitic marbles with fluids with different Fe 2O3, Al 2 O 3 and F. A fluid with low Al 2 O 3 and Fe 2O3 is assumed for the metasomatic column with wollastonite (A 1) and different Al2O3/Fe2O3 values in the fluid are responsible for the formation of columns A 2 and A 3. The stability of clinohumite or chondrodite in group C columns has been induced by a higher F of the fluid than in the other groups. The presence during the prograde metasomatic stage of distinct fluids differing by their Al 2 O 3/Fe 2O3 (columns A 2 and A 3) is likely to have been induced by variations in the source composition. Moreover, the low A1 and Fe content in column A 1 could be due to the reaction of the dolomitic marble with a fluid previously depleted in these components during percolation and reaction with the country rocks.As shown by isocon diagrams and Gresens's equation, skarn formation has locally induced both mass and volume change. The volume decreased in the wollastonite zone of A 1 (19%) and in the Fo-Cc zone of A2 (17%). Mass is always increased except in the wollastonite of A 1 where it is decreased. Mass balance of major elements has shown that Ca is likely to be a perfectly inert component and that Si is always strongly increased. Moreover, Fe is increased in A 2 and A 3 whereas Al is only increased in A 3. Mg is leached in the internal part of column Al.Quantification of chemical potential diagrams using different values of Al 2 O 3 Fe 2 O 3, X F and T suggests that the successive zones observed in all types of columns can be obtained along an increase of SiO 2 towards the inner zones. A simultaneous decrease in MgO is inferred for group A columns.  相似文献   

4.
Iron- and vanadium-bearing kyanites have been synthesized at 900 and 1100° C/20 kb in a piston-cylinder apparatus using Mn2O3/Mn3O4- and MnO/Mn-mixtures, respectively, as oxygen buffers. Solid solubility on the pseudobinary section Al2SiO5-Fe2SiO5(-V2SiO5) of the system Al2O3-Fe2O3(V2O3)-SiO2 extends up to 6.5 mole% (14mole %) of the theoretical end member FeSiO5(V2SiO5) at 900°C/20 kb. For bulk compositions with higher Fe2SiO5 (V2SiO5) contents the corundum type phases M2O3(M = Fe3+, V3+) are found to coexist with the Fe3+(V3+)-saturated kyanite solid solution plus quartz. The extent of solid solubility on the join Al2SiO5-Fe2SiO5 at 1 100°C was not found to be significantly higher than at 900° C. Microprobe analyses of iron bearing kyanites gave no significant indication of ternary solid solubility in these mixed crystals. Lattice constants a 0, b 0, c 0, and V0 of the kyanite solid solutions increase with increasing Fe2SiO5- and V2SiO5-contents proportionally to the ionic radii of Fe3+ and V3+, respectively, the triclinic angles ,, remain constant. Iron kyanites are light yellowish-green, vanadium kyanites are light green. Iron kyanites, (Al1.87 Fe 0.13 3+ )SiO5, were obtained as crystals up to 700 m in length.  相似文献   

5.
Thermal treatments of anorthite carried out at up to 1,547° C show that the unit cell parameter changes as a function of the treatment temperature. The best fit curve found by non-linear least squares analysis is: =91.419-(0.327·10-6)T 2+(0.199·10-12)T 4-(0.391·10)T 6. The results obtained support significant Al,Si disorder (Al0.10, where Al=t 1(0)-1/3 [t 1(m)+t 2(0)+t 2(m)], Ribbe 1975), in anorthite equilibrated near the melting point and confirm a high temperature series differentiated from the low temperature series for calcic plagioclases in the An85–An100 range also. In the plot vs. An-content the high and low temperature curves intersect at An85 composition and progressively diverge in the An85–An100 range. The trends of the high and low temperature curves in this range are interpretable on the basis of the degree of Al, Si order in the average structures of calcic plagioclases.  相似文献   

6.
Concentration levels of the trace elements Al, As, B, Ba, Be, Cd, Co, Cr, Cu, Li, Mo, Ni, Pb, Sr, V, Y, and Zn in the shallow Dutch ground water were studied. Data were extracted from the data base of the Dutch National Ground Water Quality Monitoring Network, a network set up to monitor the diffuse contamination. The network contains over 350 sites at a low density of about 1 per 100 km2. The sites are sampled once a year at two depths (approx. 10 and 25 m below surface). A two-step multivariate statistical approach was used, in which the major element chemistry was used to define water types. Within each water type, trace element behavior could be coupled to distinct geochemical processes: dilution, acidification and weathering, carbonate dissolution, oxidation/reduction, and ion exchange. In recently infiltrated acid rain water in low buffering capacity sands, the anthropogenic influence indirectly caused mobilization of Al (median 430 g/l), Cd (0.6 g/l), Co (14 g/l), Cu (2.7 g/l), Ni (16 g/l), Y (11 g/l), and Zn (50 mg/l). In carbonate bearing sediments the acidification is neutralized, and the mentioned trace elements remain immobile. Arsenic and Cr have higher concentrations levels in ground waters with a slightly reducing character and are possibly governed by the dissolution of iron-manganese hydroxides. Boron, Li, and Sr have high concentrations (respectively 875, 80, 2700 g/l) in the water type related to a seawater source. Strontium is related to carbonate dissolution in all other water types (medians ranging from 100 to 1000 g/l). Barium shows a complex behaviour. It is concluded that the high Al, Cd, Co, Cr, Ni, and Zn concentrations are anthropogenically induced. High Ba and Cr concentrations are inferred to be due to natural processes.  相似文献   

7.
Divariant oxide plus metal assemblages potentially make useful redox sensors for use in hydrothermal and other high pressure experiments. Here we report the calibration of the (Ni, Mn)O/Ni redox sensor in which the Ni/NiO (NNO) oxygen buffer is displaced to lower oxygen chemical potentials (O2), by the solid solution of MnO in the oxide phase. This assemblage was chosen because: (1) it covers a useful range of O2; (2) the system can be calibrated very accurately. Values of O2 defined by the (Ni, Mn)O/Ni assemblage were determined electrochemically, from 900 to 1300 K, using calcia-stabilized zirconia solid electrolytes. The oxide compositions (8 in total, ranging from 0.1X NiO0.8) were analysed afterwards by electron microprobe, and were checked for internal consistency by measuring the lattice parameters (a0), using powder XRD. The accuracies of the measurements, both assessed theoretically and established empirically, are (1): ±80J/mol in O2, ±0.0002 Å in a0 and ±0.002 to 0.005 in X NiO. Activity-composition relations were fitted to the Redlich-Kister formalism. There is a slight asymmetry (corresponding to a subregular model) across the solution with A 0 G =9577(±45) J/mol, and A 1 G =–477(±80) J/mol. The experimental data were also used to derive the parameters Vex, Hex and Sex. There is no obvious relationship between excess volumes and enthalpies of mixing, nor between excess volumes and excess entropies. The experimental data from this study have been used to formulate the (Ni, Mn)O/Ni redox sensor expression: O2 = 2(NNO) + 2RTlnX NiO + 2(1 – X NiO)2[11483 – 1.697T] – 477(4X NiO – 1)(900 < T(K) < 1300) where O2(NNO)=–478967+248.514T–9.7961 T In T, from O'Neill and Pownceby(1993a).  相似文献   

8.
The Brixen Quartzphyllite, basement of the Southern Alps (Italy), consists of metasediments which had suffered progressive deformation and low grade metamorphism (p max4 kbar, T max375±25° C) during the Palaeozoic. It has been excavated by pre-Permian erosion, buried again beneath a pile of Permo-mesozoic to Cainozoic sediments (estimated T max150° C), and is now exposed anew due to late Alpine uplift and erosion. The behavior of the K-Ar system of white micas is investigated, taking advantage of the narrow constraints on their thermal history imposed by the geological/stratigraphic reference systems.The six structurally and petrographically differing samples come from a single outcrop, whose position is roughly two kilometers beneath the Permian land-surface. White mica concentrates from five grain size fractions (<2 , 2–6 , 6–20 , 20–60 , 60–75 ) of each sample have been analyzed by the conventional K-Ar method, four selected concentrates additionally by the 40Ar/39Ar stepwise heating technique; furthermore, Ar content and isotopic composition of vein quartz were determined.The conventional ages of the natural grain size fractions (20–60 , 60–75) are in the range 316±8 Ma, which corresponds to the 40Ar/39Ar plateau age of 319.0±5.5 Ma within the error limits. The finer grain size fractions yield significantly lower ages, down to 233 Ma for fractions <2 . Likewise low apparent ages (down to 83 Ma) are obtained for the low temperature 40Ar/39Ar degassing steps.There is no correlation between microstructural generation of white mica prevailing in the sample and apparent age. This favours an interpretation of the 316±8 Ma values as cooling age; progressive deformation and metamorphism must be respectively older and their timing cannot be resolved by these methods. The data preclude any significant influence of a detrital mica component as well as of excess argon.The lower ages found for the fine grain-size fractions (respectively the low-T degassing steps) correspond to a near-surface period (p-T-minimum); the values are geologically meaningless. The effect is interpreted to result from partial Ar loss due to reheating during Mesozoic-Cainozoic reburial. A model based on diffusion parameters derived from the outgassing experiments and Dodson's (1979) equation yields a closure temperature of 284±40 °C for a cooling rate of 18° C/Ma. Furthermore, this model suggests that the observed argon loss of up to 5% may in fact have been induced by reheating to 150 °C for 50 Ma.  相似文献   

9.
A thermodynamic analysis of the intermediate solid solution (Iss) of near-cubanite composition has been attempted by considering an Fe–Zn exchange equilibrium between Iss and sphalerite. The interchange free-energy parameter of Fe–Zn mixing in Iss (WIss) and the free energy of the exchange equilibrium (G1,T ) have been deduced at 500, 600, 700 and 723° C using the compositional data of sphalerite and Iss from phase equilibrium experiments and by the standard method of linear regression analysis. For sphalerite, two independent activity-composition models have been chosen. The extracted values of G1,T and WIss, using both models, are compared. Although the values match, the errors in the extracted parameters are relatively larger when Hutcheon's model is used. Both G1,T and WIss show linear variations with temperature, as given by the following relations: G1,T = –35.41 + 0.033 T in kcal (SE=0.229)WISS= 48.451 – 0.041 T in kcal (SE=0.565) Activity-composition relations and different mixing parameters have been calculated for the Iss phase. A large positive deviation from ideality is observed in Iss on the join CuFe2S3–CuZn2S3. No geothermometric application has been attempted in this study, even though Iss of cubanite composition (isocubanite) in association with sphalerite, pyrite and pyrrhotite is reported from seafloor hydrothermal deposits. This is due to the fact that: (a) the temperatures of formation of these deposits are significantly lower than 500° C, the lower limit of appropriate experimental data base; (b) microprobe data of the coexisting isocubanite and sphalerite in the relevant natural assemblages are not available.Symbols a J i activity of component i in phase J - G1, T standard free energy change of reaction (cal) - GIM free energy of ideal mixing (cal) - GEM free energy of excess mixing (cal) - G M ex free energy of mixing (cal) - G i excess free energy of mixing at infinite dilution (cal) - i J activity coefficient of component i in phase J - i J, 0 standard chemical potential of component i in phase J (cal) - ; i J chemical potential of component i in phase J (cal) - R universal gas constant (1.98717 cal/K·mol) - T temperature in degree (K) - WJ interchange free energy of phase J in (cal) - X J i mole fraction of component i in phase J  相似文献   

10.
The chemical and microbiological characteristics of groundwater from two provinces of central Spain were studied. In some zones of this area, the concentrations of As in groundwater exceed the guideline concentrations, set internationally between 10 g/l and 50 g/l, reaching levels over 100 g/l. A narrow correlation between the contents of arsenic and HCO3– was observed. These data suggest a possible mechanism of the As mobilization from aquifer sediments to groundwater: the bicarbonate ions could displace HAsO42– adsorbed on aquifer oxyhydroxides. Sediments containing relatively high contents of adsorbed arsenic are deposited in surface water environments with low carbonate concentrations. Subsequently, the sediments become exposed to groundwater with highly dissolved carbonate content, and arsenic can be mobilized by displacement from mineral surfaces. In addition, the presence of Pseudomonas genera bacteria, which secrete siderophores (Fe chelating agents) could mobilize As adsorbed on Fe oxides through their dissolution. These combined microbiological and chemical processes might have increased the natural mobility of As.  相似文献   

11.
Single crystals of boehmite, up to 0.1 mm in size, were found in open cavities inside a corundum crystal from the Ratnapura area gem gravels in Ceylon. The unit cell parameters are (X-ray powder pattern): a 0=3.695 Å b 0=12.212 Å, c 0=2.867 Å. The crystallographic orientation is based on X-ray single-crystal precession photographs. The crystals show the faces (it010), (001), (101), and (221). Systematic extinctions agree with the space group Amam. Optical orientation: a, b, c. Refractive indices are given. The mineral is optically positive with a large optic axial angle.  相似文献   

12.
Twenty-eight samples of groundwater from bedrock boreholes in three distinct Norwegian geological provinces have been taken and analyzed for content of Rn, U, and Th, together with a wide variety of minor and major species. Median values of 290 Bq/1, 7.6 g/1, and 0.02 g/1 were obtained for Rn, U, and Th respectively, while maximum values were 8500 Bq/1, 170 g/1, and 2.2 g/1. Commonly suggested drinking water limits range from 8 to 1000 Bq/1 for radon and 14 to 160 g/1 for uranium. Radioelement content was closely related to lithology, the lowest concentrations being derived from the largely Caledonian rocks of the Trøndelag area, and the highest from the Precambrian Iddefjord Granite of southeast Norway (11 boreholes) where median values of 2500 Bq/1, 15 g/1 and 0.38 g/1, respectively, were obtained. The Iddefjord Granite is not believed to be unique in Norway in yielding high dissolved radionuclide contents in groundwaters, and several other granitic aquifers warrant further investigation in this respect.  相似文献   

13.
Two sets of measurements of the solubility of Pt and Pd in bisulfide solutions have been carried out at low temperatures. The first involved the equilibration of Pt metal with bisulfide solutions at 25 °C and pH = 6–12 for periods up to five years. These experiments yielded Pt concentrations on the order of tens of g/L at sulfide concentrations as low as 0.001 molal under conditions too reducing to permit significant contributions from hydroxide complexes. The second set of experiments consisted of reacting PtS, PdS and Au with H2S-saturated solutions having pH values of 3–4 at 25°, 50° and 90 °C. These experiments showed that the solubilities of all three metals increased with temperature. The observed order of solubility was Au > Pt Pd. Solubilities ranged from 10 to 75 g/L Au, 4 to 20 g/L Pt and 0.5 to 10 g/L Pd. The data do not permit definitive identification of the Pt and Pd species present in either set of experiments, but do strongly suggest that the species present under acidic and basic conditions are different. The measured solubility of gold at 25° and 50 °C is consistent with that measured in previous studies.Although the measured Pt and Pd solubilities are not as high as those estimated by theoretical methods, it is nevertheless evident that bisulfide complexation can lead to the remobilization of Pt and Pd over a wide range of pH under reducing conditions at geologically reasonable sulfide concentrations, at low as well as high temperatures. Such conditions are characteristic of a wide variety of geological environments where Pt and Pd have been inferred to have been affected by hydrothermal transport. In these cases, bisulfide complexation is far more effective than chloride or hydroxide complexes in transporting the PGE. On leave from: Shenyang Laboratory of Rock and Mineral Resources, Ministry of Geology and Mineral Resources, People's Republic of China  相似文献   

14.
Measurements of O2, Fe(II), Mn(II)and HS5 in salt marshsediments in the Tagus Estuary, Portugal, made with a voltammetric microelectrode, reveal strong seasonal differences in pore water composition within the 20~cm deep root zone. In spring, oxygen was below detection limit except close to the sediment surface. Fe(II) was present below 5 cm in concentrations ranging from detection limit to 1700 M. In summer, oxygen was present in the pore water almost to the bottom of the root zone in concentrations ranging from detection limit to more than 100 M. The spatial variability was intense: O2 concentrations as high as 78 M and as low as 25 M existed within 2~mm of each other. Fe(II) was below detection limit except towards the bottom of the root zone. In late fall, oxygen was found to 8 cm depth, but in concentrations lower than in summer, and Fe(II) was present below 9 cm. Mn(II) was found at levels declining from typical values of 200 M in spring to less than 20 M in late fall. With one exception, sulfide was below the detection limit in all measurements. During periods when dissolved Fe(II) is available in the pore water at the same time as 2 is delivered by roots, iron-rich concretions can form on roots. These conditions, which lead to precipitation of iron oxide in the sediment adjacent to roots, exist in spring, when new roots infiltrate anoxic Fe(II) containing sediment. They do not exist in summer, when dissolved Fe(II) is unavailable, or in winter, when oxygen is unavailable. The seasonal redox pattern revealed by the pore water chemistry is driven by the annual cycle of growth and decay of roots.  相似文献   

15.
Zusammenfassung Es wurden Kalifeldspäte aus Orthogneisen, Paragneisen und Glimmerschiefern des westlichen Tauemfensters (Hohe Tauern, Tirol) mit optischen und röntgenographischen Methoden im Hinblick auf ihren Strukturzustand untersucht.Es zeigte sich, daß in den Randbereichen des Tauemfensters in Gesteinen der Grünschieferfazies weitgehend geordneter Mikroklin mit einem optischen Achsenwinkel 2 Vx 80°, Auslöschungswinkel Z (010)=15–20°, Doppelbrechung nz-nx= 0,0065, Triklinität=0,90-–0,95, ca. 0,88 Al auf T1O-Position und einem Ab-Gehalt von ca. 5 Gew.% auftritt. Dagegen wurden in Gesteinen der schwachtemperierten Amphibolitfazies des zentralen Bereichs Orthoklase bis intermediäre Mikrokline mit stark schwankenden optischen Eigenschaften, mit Triklinitäten zwischen 0 und 0,7, 0,8 bis 0,9 Al in T1-Positionen, 0,45–0,8 Al auf T1O und Ab-Gehalten von ca. 10 Gew.% festgestellt. Die Kalifeldspatkristalle zeigen ungleichmäßige Auslöschung mit Winkeln von Z (010) zwischen 0 und 15°, 2 Vx zwischen 50 und 75° und nz-nx=0,005 bis 0,006. Teilweise ist Zonarbau mit geringerer Triklinität am Kornrande erkennbar. Diese undulös auslöschenden Kalifeldspäte enthalten einzelne schmale Lamellen von maximal triklinem Mikroklin mit Z (010)=15–20° und nz-nx= 0,006–0,007.Die Grenze zwischen dem Verbreitungsgebiet von maximalem Mikroklin einerseits und Orthoklas bis intermediärem Mikroklin andererseits verläuft in den westlichen Hohen Tauern ungefähr konform mit der Albit-Oligoklas-Grenze (Morteani &Raase, 1974) und mit der aus Sauerstoff-Isotopen-Untersuchungen bestimmten 500° C-Isotherme (Hoernes &Friedrichsen, 1974).
The potassic feldspar in orthogneisses, paragneisses, and mica schists from the western Tauernfenster (Hohe Tauern, Tyrol) were studied by optical and X-ray methods with regard to their structural state and in relation to grade of metamorphism.In the peripheral region of the Tauernfenster in greenschist-facies rocks highly triclinic microcline occurs with an optic angle 2 Vx of about 80°, extinction angle Z (010) =15–20°, birefringence nz-nx=0.0065, triclinicity=0.90–0.95, approx. 0.88 Al in T1O-site, and an Ab-content of about 5 wt.%. In the central area with rocks of the low-grade amphibolite facies, on the other hand, orthoclase to intermediate microcline with highly variable optical properties, triclinicities in the range of 0–0.7, 0.8–0.9 Al in T1-sites, 0.45–0.8 Al in T1O-site, and an Ab-content of about 10 wt.% was recognized. The K-feldspar grains have nonuniform extinction Z (010) scattering in the range of 0–15°, 2 Vx in the range of 50–75°, and nz-nx= 0.005–0.006. Sometimes a zonal structure with lower triclinicity exists at the rim. These undulatory K-feldspar grains usually contain small lamellae of highly triclinic microcline with Z (010) =15–20° and nz-nx=0.006–0.007.From the occurrence of maximum microcline and of orthoclase to intermediate microcline in the Hohe Tauern area an isograd was defined that is approximately conformable with the albite-oligoclase isograd (Morteani &Raase, 1974) and with the 500° C isotherm based on oxygen isotope analyses (Hoernes &Friedrïchsen, 1974).
Résumé Les feldspaths potassiques d'orthogneiss, de paragneiss et de micaschistes de la Fenêtre des Tauern occidental (Hohe Tauern, Tirol) ont été étudiés du point de vue de leur état structural.Dans les roches du faciès schistes verts de la région périphérique de la Fenêtre des Tauern les microclines sont caractérisés par un angle des axes optiques 2 Vp =80°, un angle d'extinction ng (010)=15–20°, une biréfringence ng-np=0,0065, une triclinicité= 0,90–0,95, 0,88 Al dans le site T1O et par une teneur en albite d'environ 5%. Au contraire, dans les roches du faciès amphibolite à faible degré de la région centrale, ont été observées des orthoses allant à des microclines intermédiaires avec des propriétés optiques très variables, un degré de triclinicité de 0 à 0,7, 0,8–0,9 Al dans les sites T1, 0,45–0,8 Al dans T1O et avec une teneur en albite d'environ 10%.Les cristaux de feldspath montrent une extinction irrégulière avec des angles Z (010) variable de 0 à 15°, 2 Vp de 50 à 75° et ng-np=0,005–0,006.On peut voir quelquefois une structure zonée avec une triclinicité moindre au bord des cristaux. Ces feldspaths potassiques contiennent de minces lamelles de microcline à triclinicité maximum, avec ng (010)=15–20° et ng-np 0,006–0,007.La limite entre les régions à microcline maximum d'une part, et à orthose ou microcline intermédiaire d'autre part, suit, dans les Hohe Tauern, sensiblement l'isograde albite-oligoclase (Morteani &Raase, 1974) et, l'isotherme de 500° C telle qu'elle fut determinée les isotopes de l'oxygène (Hoernes &Friedrichsen, 1974).
, ( , ) ., 2 Vx80°, Z (010)=15–20°, nz–nx=0,0065, =0,90–0,95, 0,88 l T1O Ab 5 .-%. , 0 0,7, 0,8-0,9 1 T1 l 10 .-%. Z V (010) 0 15°, 2 Vx 50 75° nz–nx=0,005–0,006. . Z V (010) =15-20° nz–nx=0,006–0,007. , Morteani & Raase (1974) 500° , Hoernes & Friedrichsen (1974).
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16.
Osumilitess was synthesized as a single phase product in the model system K2O-MgO-Al2O3-SiO2 at 800° C/ 0.5 Kbar water pressure and at 800° to 840° C/1.0 Kbar total pressure with 0.3 in the gas phase. The experimentally determined solid solubility range of synthetic osumilites can be expressed by the formula KMg2(Al3-xMgx) (Al2–xSi10+x)O30 with 0x0.4. A survey of sixteen chemical analyses of natural osumilites from eleven occurrences shows a solid solubility characterized by 0x0.6. Reversed stability experiments for the synthetic osumilite KMg2(Al2.75Mg0.25)(Al1.75Si10.25)O30 determined at water pressure equal to total pressure demonstrate its restriction to water pressures below 0.8 Kbar (at 0.5 Kbar, the stability range is between 765° and 800° C). At the lower thermal stability limit osumilite+H2O vapor break down to cordierite+K feldspar+phlogopitess+quartz, at the higher one to cordierite+K feldspar+phlogopite+liquid. Reduction of water fugacity will expand the stability field largely by shifting the lower and higher thermal stability limits to lower and higher temperatures, respectively. The dependence of osumilite stability on water fugacity makes osumilite a sensitive indicator mineral for dry conditions in rocks formed at total pressures higher than about 0.8 Kbar.  相似文献   

17.
The Oso Bay, Texas, sediments from nine sites were analyzed by GC-MS for organics to measure contamination in the bay. In most of the sites sediments contained tetrachloroethene (87–1433 g/kg), bis (2-ethylhexyl)phthalate (40–193 g/kg), and aliphatic hydrocarbons, C8-C13 (720–2491 g/kg). Sources of these contaminants include a landfill, military facilities, and municipal and industrial discharges. Size analysis of the sediments indicates they contain a high percentage of muddy sand (50–75 percent), which suggests that Oso Bay consists of common bay margin sediments.  相似文献   

18.
Temperatures of the formation of mud-volcanic waters are determined based on concentrations of some temperature-dependent components (Na–Li, Mg–Li). Estimates obtained for the Taman and Kakhetia regions are similar and range from 45 to 170°, which correspond to depths of 1–4.5 km. The calculated temperatures correlate with the chemical (Li, Rb, Cs, Sr, Ba, B, I, and HCO3) composition of water and 13 (2) and 13 (CH4) values in spontaneous gases. The isotope values indicate that mechanisms of the formation of 13-rich gases, i.e., gases with high 13 values (up to +16.0 in 2 and –23.4 in CH4) in mud-volcanic systems of Taman and Kakhetia are governed by fluid-generation temperatures rather than the supply of abyssal gases. The 11 value was determined for the first time in mud-volcanic products of the Caucasus region. This value ranges from +22.5 to +39.4 in the volcanic water of Georgia, from –1.2 to +7.4 in the clayey pulp of Georgia, and from –7.6 to +13.2 in the clayey pulp of Taman. It is shown that the 11 value in clay correlates with the fluid-generation temperature and 11 correlates with 13 in carbon-bearing gases. These correlations probably testify to the formation of different phases of mud-volcanic emanations in a single geochemical system and suggest the crucial role of temperature in the development of isotope-geochemical features.  相似文献   

19.
Water samples were collected from the Truckee River-Pyramid Lake system, the Walker River-Walker Lake system, and the Carson River, all located in eastern California and western Nevada, U.S.A., at three different times (i.e., summer 1991, spring 1992, and autumn 1992) over a two year period. The concentrations of As, Na, Cl, PO4, and pH were measured in these river samples and the associated terminal lakes. Arsenic values ranged from below 13 nmol/kg near Truckee, California to 160 nmol/kg at Nixon, Nevada in the Truckee River, from 40 nmol/kg in the headwaters of both West and East Walker Rivers to 270 nmol/kg below Weber Reservoir on the main branch of the Walker River, and from <27 nmol/kg to 234 nmol/kg for the lower Carson River system. Arsenic concentrations in Steamboat Creek (0.91 mol/kg–1.80 mol/kg) in the Truckee River catchment are above the U.S. EPA drinking water maximum contaminant level of 0.67 mol/kg, as are the As concentrations in both Pyramid Lake (1.33 mol/kg–1.57 mol/kg ) and Walker Lake (13.7 mol/kg–18.7 mol/kg). Sources of As for all three rivers include weathering of As-rich rocks and/or regolith and input of high-As geothermal spring waters, both processes primarily, although not exclusively, adding As to the headwater regions of these rivers. Steamboat Hot Springs (29 mol/kg As 54.5 mol/kg), for example, is identified as a source of As to the Truckee River via Steamboat Creek. The high As concentrations in Pyramid and Walker Lakes are likely due to (1) desorption of arsenate from aquatic particulate matter in these high pH waters (9.0 pH 9.5), (2) limited biologic uptake of arsenate, and (3) evaporative concentration of the lake waters. Evaluation of molar PO4}/As ratios of river waters and geothermal spring waters (e.g., Steamboat Hot Springs), indicates that phosphate is substantially enriched in Steamboat Creek as well as the mid to lower reaches of the Walker and Carson Rivers. These regions of each river are dominated by agricultural interests and, additionally, in the case of Steamboat Creek, residential areas and golf courses. Our data strongly imply that phosphate-rich agricultural return flow has likely added P to these streams and, consequently, increased their respective P:As ratios.  相似文献   

20.
Lake Suwa, located in the center of the largest Japanese island of Honshu was a typical hypertrophic lake with a dense scum Microcystis species in summer during the 1970's. However, due to the introduction of a sewage treatment plant and the awareness of environmental pollution by local residents, a decrease in the concentration of nutrients in lake water since 1981 has been observed (from 1600 g l–1 and 160 g l–1 in 1977 to 990 g l–1 and 110 g l–1 in 1984 for total nitrogen and phosphorus respectively).  相似文献   

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