首页 | 本学科首页   官方微博 | 高级检索  
相似文献
 共查询到20条相似文献，搜索用时 62 毫秒
1.
The main aspects of the geosynclinal and orogenic evolution of the Petchabun foldbelt in Central Thailand are described. This area was previously thought to be deformed by the Indosinian (Triassic) orogeny. The new data show that the main orogenic event in Thailand can be dated: Post Lower Permian — Pre Uppermost Permian. Evidence is given that Paleotethys closed on Thai territory during this orogenic event. The known Upper Triassic deformations in Northern Thailand are supposed to be strictly intracontinental and therefore of minor importance.
Zusammenfassung Die Grundzüge der geosynklinalen und orogenen Entwicklung des Faltengürtels von Petchabun werden beschrieben. Bisher wurde angenommen, daß dieses Gebiet während der Indosinischen Orogenese (Trias) deformiert wurde. Die neuen Daten belegen, daß die bedeutendste Orogenese in Thailand nach dem Unter Perm einsetzte (West-Thailand) und vor dem höchsten Perm abgeschlossen war (Petchabun). Die sog. Paleotethys wurde während dieser Orogenese hier geschlossen. Die bekannten obertriadischen Deformationen sind dagegen rein intrakontinental und somit von untergeordneter Bedeutung.
Résumé Les traits principaux du développement géosynclinal et orogénique de la ceinture plissée du Petchabun (Thailande) sont décrits. Jusqu'à présent on pensait que cette région avait été déformée pendant l'orogenèse «Indosinienne» (Trias). Les données nouvelles indiquent que l'orogenèse la plus importante a commencée après le Permien inférieur (dans l'Ouest de la Thailande) et qu'elle s'est terminée avant le Permien supérieur (région de Petchabun). Ici, la soi-disant «Paléotéthys» s'est fermée au cours de cette orogenèse. Les déformations bien connues du Trias supérieur sont exclusivement intracontinentales et n'ont ainsi qu'une signification subordonnée.
Petchabun. , (). , ( ) (Petchabun). . . .
  相似文献   

2.
Granitoids within the Precambrian basement of north-eastern and southern Somalia are subdivided on the basis of geology, geochronology and petrology into three different assemblages. The post-kinematic assemblage in north-eastern Somalia ( 630 Ma) comprises granodiorites and granites which belong to a medium-K calc-alkaline suite. Average initial Sr, Nd and Pb isotopic ratios [Sri = 0.7048, Nd = –1.8,206Pb/204Pb(i) = 17.704 and207Pb/204Pb(i) = 15.611] indicate that these melts were derived from a mantle or juvenile crustal source with only slight involvement of pre-existing crust as a contaminant. Two different assemblages are found in southern Somalia. The older assemblage is composed of crustal anatectic, synkinematic, parautochthonous granites ( 600 Ma) related to amphibolite facies retrogression of an intensively reworked pre-Pan-African crust [Sri = 0.7100, Nd = –8.4,206Pb/204Pb(i) = 15.403 and207Pb/204Pb(i) = 15.259]. These monzo- and syenogranites are moderately potassic and peraluminous. The younger assemblage ( 470 Ma) consists of post-kinematic monzonites to syenogranites with A-type affinities. Initial Sr, Nd and Pb isotopic data for this metaluminous assemblage [Sri = 0.7114, Nd = –13.1,207Pb/204Pb(i) = 16.913 and207Pb/204Pb(i) = 15.512] indicate a significant lower crustal component but, however, also a mantle signature. The late Proterozoic to early Palaeozoic granitoids in Somalia thus express contrasting regimes, characterized by strong juvenile input in the north, close to the Arabian-Nubian Shield, whereas intense crustal reworking with little addition of juvenile material prevailed in the south. Somalia was definitively not a cratonic area during the Pan-African, but a zone of high crustal mobility.  相似文献   

3.
The carbon isotopic fractionation between CO2 vapour and sodamelilite (NaCaAlSi2O7) melt over a range of pressures and temperatures has been investigated using solid-media piston-cylinder high pressure apparatus. Ag2C2O4 was the source of CO2 and experimental oxygen fugacity was buffered at hematite-magnetite by the double capsule technique. The abundance and isotopic composition of carbon dissolved in sodamelilite (SM) glass were determined by stepped heating and the 13C of coexisting vapour was determined directly by capsule piercing. CO2 solubility in SM displays a complex behavior with temperature. At pressures up to 10 kbars CO2 dissolves in SM to form carbonate ion complexes and the solubility data suggest slight negative temperature dependence. Above 20 kbars CO2 reacts with SM to form immiscible Na-rich silicate and Ca-rich carbonate melts and CO2 solubility in Na-enriched silicate melt rises with increasing temperature above the liquidus. Measured values for carbon isotopic fractionation between CO2 vapour and carbonate ions dissoived in sodamelilite melt at 1200°–1400° C and 5–30 kbars average 2.4±0.2, favouring13C enrichment in CO2 vapour. The results are maxima and are independent of pressure and temperature. Similar values of 2 are obtained for the carbon isotopic fractionation between CO2 vapour and carbonate melts at 1300°–1400° C and 20–30 kbars.  相似文献   

4.
Partitioning of F between H2O and CO2 fluids and topaz rhyolite melt   总被引：2，自引：0，他引：2  
Fluid/melt distribution coefficients for F have been determined in experiments conducted with peraluminous topaz rhyolite melts and fluids consisting of H2O and H2O+CO2 at pressures of 0.5 to 5 kbar, temperatures of 775°–1000°C, and concentrations of F in the melt ranging from 0.5 to 6.9 wt%. The major element, F, and Cl concentrations of the starting material and run product glasses were determined by electron microprobe, and the concentration of F in the fluid was calculated by mass balance. The H2O concentrations of some run product glasses were determined by ion microprobe (SIMS). The solubility of melt in the fluid phase increases with increasing F in the system; the solubility of H2O in the melt is independent of the F concentration of the system with up to 6.3 wt% F in the melt. No evidence of immiscible silica- and fluoriderich liquids was detected in the hydrous but water-undersaturated starting material glasses (8.5 wt% F in melt) or in the water-saturated run product glasses. F concentrates in topaz rhyolite melts relative to coexisting fluids at most conditions studied; however, DF (wt% F in fluid/wt% F in melt) increases strongly with increasing F in the system. Maximum values of DF in this study are significantly larger than those previously reported in the literature. Linear extrapolation of the data suggests that DF is greater than one for water-saturated, peraluminous granitic melts containing 8 wt% F at 800° C and 2 kbar. DF increases as temperature and as (H2O/H2O+CO2) of the fluid increase. For topaz rhyolite melts containing 1 wt% F and with H2O-rich fluids, DF is independent of changes in pressure from 2 to 5 kbar at 800° C; for melts containing 1 wt% F and in equilibrium with CO2-bearing fluids the concentrations of F in fluid increases with increasing pressure. F-and lithophile element-enriched granites may evolve to compositions containing extreme concentrations of F during the final stages of crystallization. If F in the melt exceeds 8 wt%, DF is greater than one and the associated magmatic-hydrothermal fluid contains >4 molal F. Such F-enriched fluids may be important in the mass transport of ore constituents, i.e., F, Mo, W, Sn, Li, Be, Rb, Cs, U, Th, Nb, Ta, and B, from the magma.  相似文献   

5.
Partial melting experiments on plagioclase (An60) and diopside have been carried out using pairs of large crystals to investigate textures and kinetics of melting. The experiments were done at one atmosphere pressure as a function of temperature (1,190–1,307° C) and time (1.5–192 h). Melting took place mainly at the plagioclase-diopside contact planes. Reaction zones composed of fine mixtures of calcic plagioclase and melt were developed from the surface of the plagioclase crystal inward. There exists a critical temperature, below which only a few % melting can occur over the duration of the experiments. This sluggish melting is caused by slow NaSi-CaAl diffusion in plagioclase, because the plagioclase crystal must change its composition to produce albite-rich cotectic melts. Diffusion in the solid also affects the chemical composition of the melts. During initial melting, potassium is preferentially extracted from plagioclase because K-Na diffusion in plagioclase is faster than that of NaSi-CaAl. This also causes a shift in the cotectic compositions. Above the critical temperature, on the other hand, melting is promoted by a metastable reaction in which the plagioclase composition does not change, and which produces melts with compositional gradients along the original An60-diopside tie line. The critical temperature is determined by the intersection of the cotectic and the An60-diopside tie line. Interdiffusion coefficients of plagioclase-diopside components in the melt are estimated from melting rates above the critical temperature by using a simplified steady-state diffusion model (e.g., 10–8 cm2/sec at 1,300° C).Many examples of reaction zones due to partial melting have been described as spongy or fingerprint-like textures in xenoliths. Metastable melting above the critical temperature is considered to take place in natural melting where there is a high degree of melting. However, we cannot exclude the possibility of disequilibrium created by sluggish melting controlled by diffusion in the minerals. If melting occurs close to the solidus, this process can be important even for partial melting in the upper mantle.  相似文献   

6.
Petrological and experimental studies demonstrated that nepheline-normative, SiO2-rich melts can be present in the upper mantle at pressures 1.5 GPa. To evaluate the role of such melts in mantle processes and magma genesis, we carried out two types of experiments: (1) melt distribution experiments to characterize the grain-scale distribution of a small fraction of typical SiO2-rich mantle melt (SRMM) in polycrystalline olivine (Ol) at 1,180°C, 1.2 GPa; and (2) an infiltration experiment to test the ability of SRMM to impregnate and metasomatise neighbouring non-molten mantle rocks. The median dihedral angles at Ol-Ol-SRMM contacts are equal to 50°, implying that melt should be interconnected at all melt fractions. Complications arise, however, in the investigated system because Ol–liquid interfacial energy is anisotropic, and we estimate that the connectivity threshold in the SRMM–Ol system is 0.3 vol%. Regarding the very low volume fraction of SRMM in peridotites, we conclude that these melts either occur as isolated pockets or form a network of grain edge channels with a low degree of connectivity due to a large number of dry grain edges. Even in the case where an interconnected network exists, their large viscosities should prohibit the extraction of SRMM from peridotite sources. The infiltration experiment also points to a very reduced mobility of SRMM in the upper mantle. In this experiment, a slice of synthetic dunite was immersed into a magma reservoir made of 60 wt% SRMM+40 wt% Ol, and subjected to 1,180°C-1.2 GPa for 113 h: despite this long duration, the SiO2-rich liquid was unable to infiltrate measurably the dunite. Our experiments do not support the hypothesis that SRMM represent agents of mantle metasomatism.  相似文献   

7.
CaO-rich, Al2O3-poor ultracalcic primitive melts occur at mid-ocean-ridges, back-arc basins, ocean islands and volcanic arcs. They are subdivided into a nepheline-normative alkaline-rich, silica-poor group uniquely found in arcs and in hypersthene-normative fairly refractory melts which occur in all of the above environments. The high CaO contents (to 19.0 wt%) and CaO/Al2O3 ratios (to 1.8) exclude an origin from fertile lherzolites at volatile-absent conditions. Experimental investigation of the liquidus of a hypersthene-normative and a nepheline-normative ultracalcic melt results in quite distinct pressure-temperature conditions of multiple saturation: whereas the hypersthene-normative liquid saturates in olivine + clinopyroxene at 1.2 GPa and 1,410°C, this occurs at 0.2 GPa and 1,220°C for the nepheline-normative ultracalcic liquid. Our results in combination with melting experiments from the literature suggest that hypersthene-normative melts result from melting of a refractory olivine + clinopyroxene ± orthopyroxene source at elevated mantle temperatures. Contrasting, nepheline-normative ultracalcic melts form from wehrlitic cumulates in the arc crust; to account for the high alkaline and low silica contents, and the relatively low temperatures, source wehrlites must have contained amphibole.  相似文献   

8.
Bulk diffusion of iron in synthetic dunites containing 1–6 vol.% fluid or melt at 10 kbar (1 GPa) and 900°–1300° C was examined by encapsulating the samples in platinum, which served as a sink for iron. The rate of iron loss from the dunite was found to depend strongly upon the identity of the fluid, which was varied from CO2 and H2O to melts of basaltic and sodium carbonate composition. Carbon dioxide in amounts up to 4 vol.% has no effect upon bulk iron diffusion because it exists in the dunite are isolated pores. The interconnected nature of H2O, basaltic melt, and carbonate melt, on the other hand, results in marked enhancement of bulk-rock Fe diffusion that is correlated with the diffusivity and solubility of olivine components in the fluid. At 1300° C, 4–5 vol.% of either water or basaltic melt increases the effective bulk diffusivity from the fluidabsent value of 10-10 cm2/s to 10-8 cm2/s. A single experiment involving a similar volume fraction of carbonate melt yielded a minimum bulk diffusivity of 10-7–10-6 cm2/s. This remarkably high value is attributable to the concurrent high diffusivity and high solubility of olivine components in molten carbonate H2O has a high diffusivity, estimated at 10-4 cm2/s in this study, and basaltic melt can dissolve large amounts of olivine, but neither possesses these two qualities in combination. Bulk transport of Fe in dunite containing <2 vol.% of pure H2O is independent of olivine grain size for samples having an average grain diameter of <10 m to 60 m. This is probably because bulk diffusion specifically in these H2O-bearing samples is ratelimited by the flux (which is proportional to concentration) of olivine components in the fluid. Given a constant fluid volume fraction, the effect of reducing the grain size is to increase the number of fluid-filled channels, but at the same time to decrease their average aperture, thus keeping constant the cross-sectional area through which the diffusional flux occurs. (Independence of bulk diffusivity from grain size is not anticipated for rocks containing melt, in which the silicate components are much more soluble.) In numerical (finite difference) simulations of selected laboratory experiments, the bulk Fe transport process was modeled as diffusion in fluid-filled tubules of triangular cross-section that are supplied by volume diffusion from contacting olivine grains with which they are in surface equilibrium. Applying a tortuosity factor of 1.7 brings the numerically computed diffusional loss profiles for experiments containing basaltic melt into near-coincidence with the experimentally-determined curves. This success in reproducing the experimental results lends credence to the interpretation of the bulk diffusional loss profiles as composites of gradients due to volume, grain-boundary and fluid-phase diffusion.  相似文献   

9.
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   

10.
Ground waters in North Hesse (Germany) are conspicuous by high amounts of dissolved inorganic carbon (DIC) at low pH. The DIC is received from the uptake of soil CO2 and CO2 of volcanic origin and the subsequent dissolution ofTriassic and Permian limestone and dolomites. The volcanic CO2 is related to Miocene basaltic magma which has liberated gaseous CO2 during thebreakthrough to Triassic and Permian sediments. The volcanic CO2 (-6 < 13CCO2 < -3, PDB) was trapped within pore spacesand intra- and intergranulares of Permian evaporites and Triassic sandstones and was stored within such reservoirs until recent times. The uptake of volcanic CO2 occurs as ground water migrates through such reservoirs. The 13 C/12 C-signatures of the DIC indicate mixture of soil-CO2and CO2 of volcanic origin for the dissolution of marine limestone and dolomites. The obtained two types for CO2 of volcanic origin with 13CCO 2-values of -10 ± 3 and +2 ± 2 can be explained by diffusion of CO2 through micropores, faults, and interfacesof solids. This mobilisation of CO2 is accompanied with a kinetic fractionation of -9. 13 C-depleted CO2 is liberated from the reservoir,whereas 13 CO2 is accumulated in the residue  相似文献   

11.
Basalt contamination by continental crust: Some experiments and models   总被引：1，自引：1，他引：1  
Chemical interaction between molten basalt and felsic minerals of the continental crust (quartz, K-feldspar, and oligoclase) was examined in static and dynamic experiments at 1,200°–1,400° C. Under circumstances of continuous stirring at 1,400°, -quartz dissolves in tholeiite melt at a rate of 3.3×10–6 g/s per cm2 of contact area; at 1,300°, the solution rate is 1.5×10–6 g/cm{cm2}s. The feldspars are molten at the experimental conditions, and interact with contacting basalt melt by diffusion in the liquid state. This is a complex process characterized by rapid initial diffusion of alkalies to establish a distribution between felsic melt and basalt similar to that observed in cases of actual two-liquid equilibrium (both alkalies reach concentrations in the felsic melt 1.5–3 times those in the basalt). Alkali diffusion may be uphill or downhill, depending on which direction of net flux is required to produce a two-liquid type distribution. Once this distribution is attained, subsequent diffusion of all melt species is slow and apparently limited by the diffusivity of SiO2, which is 10–9-l0–10 cm2/s at 1,200° C. Interdiffusion experiments involving molten basalt and synthetic granite confirm the behavior illustrated by the feldspar/basalt results, and give similar SiO2 diffusivities.The solution rates and interdiffusion data can be used to model basalt contamination processes likely to occur in the continental crust. For the restricted case of solid quartzitic xenoliths, the uptake of SiO2 in a well-mixed basalt magma is quite fast: appreciable SiO2 contamination may occur over exposure times of only days to years. If basalt magma induces local melting of crustal rocks, the assimilation process becomes one of liquid-state interdiffusion. In this case, the varying diffusivities of ions and their differing preferences for silicic relative to basaltic melts can produce marked selective contamination effects. Selective contamination of ascending basaltic magmas is particularly likely in the case of K2O, which may be introduced in substantial amounts even when other elements remain unaffected. The Na2O content of mantle-derived magmas is buffered against contamination by crustal materials, and K2O is buffered against further increases once it reaches a level of 1–1.5 wt.%.  相似文献   

12.
Experiments designed to simulate the dissolution of alkali feldspar during magma mixing produced plagioclase mantles that are texturally and compositionally similar to those in some hybrid volcanic rocks. In hydrous dacite melt (69% SiO2) at 0.8 GPa, 850°C, orthoclase (Or93) and sanidine (Or30) partially dissolved and were mantled by sodic plagioclase (An25–30). Although plagioclase nucleated epitaxially as a thin shell on the alkali feldspar surface near the time of initial resorption, plagioclase subsequently grew inward —mostly in the form of parallel blades — toaard the receding dissolution surface. Orthoclase dissolved at a rate approximately proportional to the square root of run duration, indicating diffusional control. Plagioclase grew inward within a static boundary zone of melt that formed between the original crystal-dacite interface and the dissolution surface. During orthoclase dissolution, this boundary zone rapidly and simultancously gained Na (by diffusion from dacite) and lost K (by diffusion into dacite); Ca diffused more slowly into this zone, from which non-feldspar species were mostly excluded. Plagioclase was stable where sufficient Ca had diffused in that the boundary zone melt intersected the plagioclase-saturation liquidus. Plagioclase subsequently grew toward the receding dissolution surface as the Ca compositional gradient (and hence the site of plagioclase saturation) stepped inward. Crystallization of plagioclase in the form of parallel blades allowed continued diffusive exchange of melt components between the dissolution surface and the host melt. Bladed growth also served to maintain (at blade tips) proximity of plagioclase to the dissolution surface, thereby apparently preserving (locally) a thin zone of low-variance melt. In natural systems, mantling of alkali feldspar by plagioclase will occur in a similar manner when (a) P, T, or X are changed to induce alkali feldspar dissolution, (b) sufficient Ca is available in the host melt to drive (by diffusion) boundary zone melt compositions to plagioclase saturation, and (c) temperatures are low enough to stabilize sodic plagioclase and to maintain a coherent boundary zone. These reqjirements are satisfied in volcanic systems when alkali feldspar is juxtaposed during mixing with hybrid melts of dacitic composition. Mantled feldspars in some intrusive systems (i.e., rapakivi granites) may form by a similar dissolution- and diffusion-controlled mechanism. Textural evidence of a similar origin may be obscurred in intrusive rocks, however, by products of late-stage magmatic and subsolidus processes.  相似文献   

13.
Solubility and solution mechanisms in silicate melts of oxidized and reduced C-bearing species in the C-O-H system have been determined experimentally at 1.5 GPa and 1400 °C with mass spectrometric, NMR, and Raman spectroscopic methods. The hydrogen fugacity, fH2, was controlled in the range between that of the iron-wüstite-H2O (IW) and the magnetite-hematite-H2O (MH) buffers. The melt polymerization varied between those typical of tholeiitic and andesitic melts.The solubility of oxidized (on the order of 1-2 wt% as C) and reduced carbon (on the order of 0.15-0.35 wt% as C) is positively correlated with the NBO/Si (nonbridging oxygen per silicon) of the melt. At given NBO/Si-value, the solubility of oxidized carbon is 2-4 times greater than under reducing conditions. Oxidized carbon dioxide is dissolved as complexes, whereas the dominant reduced species in melts are CH3-groups forming bonds with Si4+ together with molecular CH4. Formation of complexes results in silicate melt polymerization (decreasing NBO/Si), whereas solution of reduced carbon results in depolymerization of melts (increasing NBO/Si).Redox melting in the Earth’s interior has been explained with the aid of the different solution mechanisms of oxidized and reduced carbon in silicate melts. Further, effects of oxidized and reduced carbon on melt viscosity and on element partitioning between melts and minerals have been evaluated from relationships between melt polymerization and dissolved carbon combined with existing experimental data that link melt properties and melt polymerization. With total carbon contents in the melts on the order of several mol%, mineral/melt element partition coefficients and melt viscosity can change by several tens to several hundred percent with variable redox conditions in the range of the Earth’s deep crust and upper mantle.  相似文献   

14.
The diffusion of water in natural obsidian and model dacitic melts (Ab90Di8Wo2, mol %) has been studied at water vapor pressure up to 170 MPa, temperatures of 1200°C, H2O contents in melts up to ～6 wt % using a high gas pressure apparatus equipped with a unique internal device. The experiments were carried out by a new low-gradient technique with application of diffusion hydration of a melt from fluid phase. The water solubility in the melts and its concentration along $C_{H_2 O} $ diffusion profiles were determined using IR microspectrometry by application of the modified Bouguer-Beer-Lambert equation. A structural-chemical model was proposed to calculate and predict the concentration dependence of molar absorption coefficients of the hydroxyl groups (OH?) and water molecules (H2O) in acid polymerized glasses (quenched melts) in the obsidian-dacite series. The water diffusion coefficients $D_{H_2 O} $ were obtained by the mathematical analysis of concentration profiles and the analytical solution of the second Fick diffusion law using the Boltzman-Matano method. It was shown experimentally that $D_{H_2 O} $ exponentially increases with a growth of water concentration in the obsidian and dacitic melts within the entire range of diffusion profiles. Based on the established quantitative correlation between $D_{H_2 O} $ and viscosity of such melts, a new method was developed to predict and calculate the concentration, temperature, and pressure dependences of $D_{H_2 O} $ in acid magmatic melts (obsidian, rhyolite, albite, granite, dacite) at crustal T, P parameters and water concentrations up to 6 wt %.  相似文献   

15.
The equilibrium distribution of hydrous silicic melts in polycrystalline aggregates of quartz was characterized in a series of partial melting and melt distribution experiments in the systems quartz-albite-orthoclase-H2O and quartz-anorthite-H2O, at 650 to 1000 MPa and 800 to 900° C. Near-equilibrium textures in these experiments are characterized by very low quartz-quartz-melt wetting angles, and by a substantial number of thin melt films along grain boundaries. Wetting angles in the H2O-saturated experiments are as follows: 18° at 800° C-1000 MPa, and 12° at 900° C-1000 MPa in the granitic system; 18° at 850° C-650 MPa, 15° at 900° C-650 MPa, and 15° at 900° C-1000 MPa in the quartzanorthite system. In the granitic system at 900° C-1000 MPa, a decrease of H2O content in melt from 17 wt% (at saturation) to 6 wt%, results in a slight increase of wetting angle from 12° to 16°. These low wetting angles — and the observation that many grain boundaries are wetted by melt films-indicate that the ratio of quartz-quartz to quartz-melt interfacial energies (ss/s1) is high: 2. Secondary electron imaging of fracture surfaces of melt-poor samples provided a three-dimensional insight into the geometry of melt; at low melt fraction, melt forms an interconnected network of channels along grain edges, as predicted for isotropic systems with wetting angles below 60°. This high-permeability geometry suggests that the segregation of granitic melts is not as sluggish as previously anticipated; simple compaction calculations for a permeability range of 10-12 to 10-9 m2 indicate that segregation may operate at low to moderate melt fractions (below 30 vol. %), within relatively short time-scales, i.e., 105 to 106 years. Quartzmelt textures show significant deviations from the equilibrium geometries predicted for isotropic partially molten systems. The most consistent deviation is the pervasive development of crystallographically-controlled, planar faces of quartz; these faces provide definitive evidence for non-isotropic quartz-melt surface energy. For most silicates other than quartz, the grain-scale distribution of partial melts deviates even more significantly from equilibrium distributions in isotropic systems; accordingly, in order to describe adequately melt distributions in most natural source regions, the equilibrium model should be modified to account for anisotropy of solid-liquid interfacial energy.Contribution CNRS-INSU-DBT no 651  相似文献   

16.
The wetting angle between silicate melts containing Ca, Li, Na, or K and olivine single crystals have been measured as part of an investigation of the dependence of the solid-liquid interfacial energy on melt composition and olivine orientation. The wetting angle increases with increasing silica content of the melt on (100) surfaces, but decreases with increasing silica content on (010) and (001) surfaces. For a given silica content, the wetting angle on (100) decreases in going from Ca to Li to Na to K, while the wetting angle on (010) and (001) increases in going from Ca to K-bearing melts. Based on published values for liquid-vapor interfacial energies, the observed changes in wetting angle with changes in melt composition indicate that the solid-liquid interfacial energy increases with increasing silica content of the melt for the (100) surface. However, for (010) and (001) surfaces, the variation of the solid-liquid interfacial energy with silica content depends upon whether Ca or K is present in the melt. In addition, the solid-liquid interfacial energy depends upon the orientation of the olivine in the following manner: sl (010) sl (001) sl (100) .  相似文献   

17.
The results of high pressure experiments on diffusion and Soret separation in natural silicate melts show that the diffusive behaviour between natural silicic and mafic magmas can be approximately modelled as if the system were a binary mixture of SiO2 and other components such as MgO+FeO+CaO. Steady state compositional profiles across a diffusive interface between silicic and mafic magma layers are calculated on the basis of phenomenological relationships for the fluxes of chemical species and heat in the binary mixtures, using the experimental data of diffusion and Soret coefficients in natural silicate melts. The compositional profiles show a curvature with a minimum SiO2 value within the interface due to the Soret effect and temperature dependence of diffusion coefficient. The compositional gradient at the lower half of the diffusive interface is similar to that resulting from the Soret separation of a mafic melt regardless of the composition of the silicic magmas. These results suggest that picritic magma can be formed in the interfacial region between the mafic and silicic magma layers. The compositional gradient explains chemical variation of mafic to picritic inclusions in a mixed andesite of the Abu Volcano Group, Japan.  相似文献   

18.
Zusammenfassung Für Simulationsrechnungen der Gezeiten erdgeschichtlicher Ozeane werden hinreichend detaillierte paläogeographische Karten vorgestellt, die global die ungefähre Lage der ozeanischen und kontinentalen Bereiche sowie paläobathymetrische Informationen wiedergeben.Ausgehend von vorhandenen paläokontinentalen Karten, die auf den modernen Konzepten der Plattentektonik und des sea-floor spreading basieren, sind für einige erdgeschichtliche Stadien die einstige Verteilung von Land, Flachmeer und Tiefsee dargestellt. Mittels zusammengefaßter Ergebnisse paläobiogeographischer, geotektonischer, geophysikalischer, sedimentologischer und palökologischer Untersuchungen sind paläogeographische Rekonstruktionen für ein pleistozänes Hochglazial (Saale-Eiszeit), für die Obere Kreide (Ober-Campan), für das Obere Perm (Zechstein) sowie für das Mittlere Silur (Wenlock) abgebildet.Die Problematik bei der Rekonstruktion von Paläozeanen sowie die Interpretation und Kompilation paläogeographischer Daten wird diskutiert.
For modeling the paleotides of ancient oceans you need quiet detailed paleogeographical maps projecting the global distribution of oceanic and continental areas as well as some paleobathymetrical informations. Using available paleocontinental maps which are based upon the modern concepts of the plate tectonics and sea-floor spreading, ancient distributions of land, shallow and deep sea are presented for some geological stages. By means of compiling the results of paleobiogeographical, geotectonical, geophysical, sedimentological, and paleoecological investigations paleogeographical reconstructions are shown for a Pleistocene ice-age (Saale stage), the Upper Cretaceous (Upper Campanian), the Upper Permian (Zechstein), and for the Middle Silurian (Wenlockian).Problems of paleoceanical reconstructions as well as the interpretation and compilation of paleogeographical data are discussed.
Résumé Des cartes paléogéographiques à point détaillées sont présentées pour le calcul des marées des anciens océans; elles reproduisent globalement la situation approximative des domaines océaniques et continentaux, et donnent aussi des informations paléobathymétriques.Partant de cartes paléocontinentales existantes basées sur les concepts modernes de tectonique de plaques et d'expansion des océans, on a figuré pour quelques périodes géologiques la répartition ancienne des terres, des mers intérieures et des mers profondes. Utilisant les données condensees provenant des recherches paléobiogéographiques, géotectoniques, géophysigues, sédimentologiques et paléoécologiques, on a effectué les reconstructions paléogéographiques relatives à un Pleistocene glaciaire ancien (stade de la Saale), au Crétacique supérieur (Campanien supérieur), au Permien supérieur (Zechstein), ainsi qu au Silurien moyen (Wenlockien).Le problème concernant la reconstruction des paléoocéans ainsi que les interprétations et compilations des données paléogéographiques sont discutés.
- , , . , , , . , , , ( ), ( ), () ( ). , , .
  相似文献   

19.
We have experimentally investigated the phase and melting relations of garnet + clinopyroxene + carbonate assemblages at 2.5–5.5 GPa, to assess the feasibility of carbonated eclogite as a source for some crustally emplaced carbonatites. The solidus of our composition was at 1,125 °C at 2.5 GPa, 1,225 °C at 3.5 GPa and 1,310 °C at 5.0 GPa. Melts were sodic calcio-dolomitic carbonatites, and were markedly more calcic than the dolomitic melts produced by partial melting of carbonated peridotite. Na contents of the experimental carbonatites decreased with increasing pressure when compared at similar degrees of melting, and SiO2 contents increased with degree of melting. Experiments on a second composition with enhanced Na2O demonstrated its strong effect in lowering melting temperatures in carbonate eclogite. Natural carbonated eclogite bodies in the peridotitic upper mantle will have a range of solidus temperatures. In many cases, carbonate will be molten in the upper 250 km. Carbonate melt would segregate from its source eclogite at very low melt fractions and infiltrate surrounding peridotitic wall rock. This would result in metasomatic enrichment of the peridotitic wall rock, but its exact nature will depend on the relative P–T positions of the eclogite + CO2 and peridotite + CO2 solidii. As a result of these inevitable metasomatic interactions, it is considered unlikely that carbonatite melts derived from carbonated eclogite in the upper mantle could be emplaced into the crust unmodified. However, they may have a role in metasomatically enriching and carbonating parts of the upper mantle, producing sources suitable for subsequent production of silica undersaturated silicate liquids and carbonatites ultimately emplaced in the crust.Editorial responsibility: J. Hoefs  相似文献   

20.
Résumé Nous présentons les premiers résultats obtenus sur la distribution du potassium en surface et en profondeur dans les formations morainiques, d'âge quaternaire de la région d'Evian. Les mesures ont été réalisées par l'un de nous (Ph.Olive) en opérant par spectrométrie gamma. Les échantillons ont été prélevés dans 5 sondages carottés dont l'étude détaillée fait l'objet de la thèse de l'un de nous (B.Blavoux).Les résultats obtenus montrent que la teneur en potassium varie dans le même sens que le pourcentage de la fraction fine (inférieure à 40 ), et inversement à la calcimétrie totale exprimée en % du sédiment. Le dosage du potassium permet ainsi de distinguer un sédiment morainique d'un sédiment interglaciaire.
We present the first results concerning potassium surface and depth-distribution in morainic formations of quaternary age in the Evian area. Measurements were made by one of us (Ph. Olive) by means of gamma spectroscopy. Samples were collected through 5 core-drillings of which a schematic geological section is shown; a thesis has been devoted by one of us (B.Blavoux) to the detailed study of these drillings.According to the results of our research, the potassium content varies with the percentage of fine fraction below 40 and in inverse ratio to total calcimetry as expressed in % of sediment.
Zusammenfassung Wir veröffentlichen die ersten Resultate über die Oberflächen- und Tiefen-Kaliumvorkommen in den Moränenformationen des Quartärs aus der Umgebung von Evian. Die Messungen werden vonPh. Olive durchgeführt und zwar mit Hilfe der Spektranalyse der Gammastrahlen. Die Proben entnahmen wir fünf Kernbohrungen, die wir in einem schematischen geologischen Schnitt zeigen, deren detaillierte Auswertung aber Thema der Dissertation eines unserer Mitarbeiter ist (B.Blavoux).Die gefundenen Resultate zeigen, daß der Kaliumgehalt parallel zum Prozentsatz an Feinbruch (kleiner als 40 ) variiert, und reziprok zur Calcimétrie totale, gemessen in Sedimentsprozenten. Die Bestimmung des Kaliumgehaltes erlaubt also, ein Moränensediment von einem Sediment der Zwischeneiszeit zu unterscheiden.
a Evian '. .
  相似文献   

设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号