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1.
A model for trondhjemite genesis is proposed where granite is transformed to trondhjemite via infiltration by a Na-rich metamorphic fluid. The Rockford Granite of the Northern Alabama Piedmont serves as the case example for this process and is characterized as a synmetamorphic, peraluminous trondhjemite-granite suite. The major process operative in the conversion of granite to trondhjemite involves cation exchange of Na for K in the feldspar and mica phases through a volatile fluid medium. Whole-rock 18O values for the trondhjemites are negatively correlated with atomic proportion K/Na ratio indicating a partial reequilibration of the altered granitoids with a Na- and18O-rich metamorphically derived fluid. Biotite decomposition to an Al-epidote-paragonitic muscovite-secondary quartz assemblage is also associated with the sodium metasomatism, as are apatite replacement by Al-epidote and secondary zircon crystallization. Rare albitization of primary magmatic plagioclase and discontinuous grossularite reaction rim growth on magmatic garnet are present in the trondhjemites indicating the mobility of Ca during alkali metasomatism. The replacement of magmatic phases by me tasomatic phases exemplifies the chemical changes produced during infiltration metasomatism where the trondhjemites are depleted in P2O5, Th, Rb, U, K2O, V, Sn, F, MgO, Pb, TiO2, FeO* and Li and enriched in CaO, Na2O, Zr and Sr relative to the granites. Other elements, such as Cr, MnO, Cu, Zn, Co, Ba, SiO2, Ni, Al2O3, are shown to be relatively immobile during the metasomatism. The infiltration metasomatism probably occurred during prograde regional metamorphism, when a discrete fluid phase was produced in the surrounding amphibolite-grade metasediments. Foliation planes in the granite apparently served as conduits for fluid flow with reaction-enhanced permeability accompanying the 8% molar volume reduction during Na-for-K exchange in the feldspars. A source for the Na and Sr in the metamorphic fluid may have been paragonitic muscovite in the metasedimentary country rocks. Rubidium and K were probably retained in metasedimentary biotite. The Silent Lake pluton in southeastern Ontario is a possible analogue to the alkali metasomatic processes affecting the Rockford Granite.  相似文献   

2.
Recent experimental studies have shown that the rates of Al–Si order-disorder and interdiffusion in alkali feldspars at high pressures under dry conditions increase dramatically in the approximate pressure range 7–14 kb, depending on temperature and feldspar composition (Goldsmith 1987, 1988). Enhancement of Al–Si interdiffusion rates is ascribed to the involvement of hydrogen, but the species of hydrogen involved is undetermined.A simple kinetic analysis of the data of Goldsmith (1987) on disordering of dry albite at 800°–950° C and 6–24 kb in the solid media press is consistent with the NaCl pressure cell acting as a proton donor by enhancing dissociation of water in the pressure medium, generating a high in the experimental environment. The rate constant for disordering of albite is found to increase linearly with the estimated experimental and with the density of aqueous salt solution, implicating H+ as the rate-enhancing species.Further experimental studies confirm the importance of . At 16 kb and 850° C, dry albite in sealed Pt capsules in a NaCl cell containing tantalum powder (which reduces H2O to H2) remains highly ordered over the same time that complete disordering would occur in the absence of Ta. H2 cannot therefore be the rate-enhancing species. At 1 kb and 850° C, the extent of Al–Si disorder in albite in direct contact with various NaCl–H2O solutions increases from partially disordered for pure H2O to completely disordered for saturated aqueous NaCl solution, giving strong support to the proton model. SIMS scanning ion imaging of albite run products demonstrates conclusively that solution-reprecipitation is not responsible for enhanced disordering rates.Results of disordering experiments in the solid media apparatus cannot be duplicated in Ar gas media internally-heated pressure vessels, even with the same experimental configuration around the albite-bearing capsules, due to the different proton-buffering capacities of the solid and gas media apparatus.  相似文献   

3.
Near-liquidus melting experiments were performed on a high-K latite at fO2's ranging from iron-wustite-graphite (IWG) to nickel-nickel oxide (NNO) in the presence of a C-O-H fluid phase. Clinopyroxene is a liquidus phase under all conditions. At IWG , the liquidus at 10 kb is about 1,150° C but is depressed to 1,025° C at NNO and . Phlogopite and apatite are near-liquidus phases, with apatite crystallizing first at pressures below 10 kb. Phlogopite is a liquidus phase only at NNO and high . Under all conditions the high-K latites show a large crystallization interval with phlogopite becoming the dominant crystalline phase with decreasing temperature. Increasing fO2 affects phlogopite crystallization but the liquidus temperature is essentially a function of . The chemical compositions of the near-liquidus phases support formation of the high-K latites under oxidizing conditions (NNO or higher) and high . It is concluded from the temperature of the H2O-saturated liquidus at 10 kb, the groundmass: crystal ratio and presence of chilled latite margins around some xenoliths that the Camp Creek high-K latite magma passed thru the lower crust at temperatures of 1,000° C or more.  相似文献   

4.
In the Ultevis District, Northern Sweden, viridine occurs in a potassium rich, microcline-bearing leptite together with quartz, plagioclase, phlogopite, opaques, and a retrogradely formed muscovite. The formation of viridine in this rock may be described by a dealkalization process of microcline, in which opaque minerals are involved. A diffusion of K+ and H2O out of the centres of viridine formation and of H+ into these localities, which is a prerequisite of such type of reaction, may have been favoured by a contemporaneous migmatization of the rock, since the granite-like melts can be regarded as sinks for potassium and water. The following decomposition of viridine is initiated by the reverse reaction. Texturally this is indicated by small microcline seams along the contacts between viridine and quartz grains. The final alkalization of the viridine-quartz assemblage to form muscovite reflects increasing K+/H+-ratios and H2O-contents of the vapor phase and/or decreasing temperatures. The potassium and water amounts necessary for the viridine decomposition reactions may have been generated by the cooling of the granitic liquids. An intergrowth of sillimanite and the muscovite can be described by a degenerated reaction. It can be interpreted as giving way to an equilibration of the alumosilicates und the actual metamorphic conditions, that is here P, T, , a k +, a h + and a Mn 3+.The viridine investigated has the lowest Mn-contents recorded so far for andalusite-type minerals with viridine optics (1.3–2.2 mol-% Mn2SiO5-component). Since no andalusite with lower Mn-contents occurs in the rock and since no other Al2SiO5-phase formed at this metamorphic stage it may be assumed that the incorporation of manganese stabilizes the andalusite structure under the P-, T-, –, a k +-, a h +- and a Mn 3+-conditions verified in this particular leptite.The temperature of viridine formation is estimated to be about 600 ° C, the decomposition of viridine +quartz into the muscovite-sillimanite assemblage may have happened between 650–500 ° C at 6–2.5 kb.  相似文献   

5.
Redox states of lithospheric and asthenospheric upper mantle   总被引：31，自引：7，他引：24  
The oxidation state of lithospheric upper mantle is heterogeneous on a scale of at least four log units. Oxygen fugacities ( ) relative to the FMQ buffer using the olivine-orthopyroxene-spinel equilibrium range from about FMQ-3 to FMQ+1. Isolated samples from cratonic Archaean lithosphere may plot as low as FMQ-5. In shallow Proterozoic and Phanerozoic lithosphere, the relative is predominantly controlled by sliding Fe3+-Fe2+ equilibria. Spinel peridotite xenoliths in continental basalts follow a trend of increasing with increasing refractoriness, to a relative well above graphite stability. This suggests that any relative reduction in lithospheric upper mantle that may occur as a result of stripping lithosphere of its basaltic component is overprinted by later metasomatism and relative oxidation. With increasing pressure and depth in lithosphere, elemental carbon becomes progressively refractory and carbon-bearing equilibria more important for control. The solubility of carbon in H2O-rich fluid (and presumably in H2O-rich small-degree melts) under the P,T conditions of Archaean lithosphere is about an order of magnitude lower than in shallow modern lithosphere, indicating that high-pressure metasomatism may take place under carbon-saturated conditions. The maximum in deep Archaen lithosphere must be constrained by equilibria such as EMOG/D. If the marked chemical depletion and the orthopyroxene-rich nature of Archaean lithospheric xenoliths is caused by carbonatite (as opposed to komatiite) melt segregation, as suggested here, then a realistic lower limit may be given by the H2O +C=CH4+O2 (C-H2O) equilibrium. Below C –H2O a fluid becomes CH4 rather than CO2-bearing and carbonatitic melt presumably unstable. The actual in deep Archaean lithosphere is then a function of the activities of CO2 and MgCO3. Basaltic melts are more oxidized than samples from lithospheric upper mantle. Mid-ocean ridge (MORB) and ocean-island basalts (OIB) range between FMQ-1 (N-MORB) and about FMQ +2 (OIB). The most oxidized basaltic melts are primitive island-arc basalts (IAB) that may fall above FMQ+3. If basalts are accurate probes of their mantle sources, then asthenospheric upper mantle is more oxidized than lithosphere. However, there is a wide range of processes that may alter melt relative to that of the mantle source. These include partial melting, melt segregation, shifts in Fe3+/Fe2+ melt ratios upon decompression, oxygen exchange with ambient mantle during ascent, and low-pressure volatile degassing. Degassing is not very effective in causing large-scale and uniform shifts, while the elimination of buffering equilibria during partial melting is. Upwelling graphite-bearing asthenosphere will decompress along -pressure paths approximately parallel to the graphite saturation surface, involving reduction relative to FMQ. The relative will be constrained to below the CCO equilibrium and will be a function of . Upwelling asthenosphere whose graphite content has been exhausted by partial melting, or melts that have segregated and chemically decoupled from a graphite-bearing residuum will decompress along -decompression paths controlled by continuous Fe3+-Fe2+ solid-melt equilibria. These equilibria will involve increases in relative to the graphite saturation surface and relative to FMQ. Melts that finally segregate from that source and erupt on the earth's surface may then be significantly more oxidized than their mantle sources at depth prior to partial melting. The extent of melt oxidation relative to the mantle source may be directly proportional to the depth of graphite exhaustion in the mantle source.  相似文献   

6.
The alkalic ultramafic Batbjerg intrusion of East Greenland contains rocks in which nepheline and leucite are important constituents. In addition, there are vermicular, finger print intergrowths of nepheline with potassium feldspar, and patchy to micrographic intergrowths of kalsilite with potassium feldspar. The history of the pseudoleucite problem is reviewed, and it is suggested that the term pseudoleucite be restricted to intergrowths of nepheline with alkali feldspar that appear to be pseudomorphs with the crystal morphology of leucite. It is further suggested that flame-like or feather-like finger print intergrowths of nepheline with alkali feldspar, that are either interstitial to the other minerals of the rock or have grown perpendicularly on relative large and often euhedral nepheline grains are an entirely different problem and are best explained by late-stage magmatic crystallization within the system NaAlSiO4-KAlSiO4-SiO2-H2O.In the Batbjerg intrusion the early crystallization of nepheline was followed by the co-crystallization of nepheline with leucite, or in some cases by nepheline and a silica-rich leucite. Although the magma was essentially dry, as indicated by the dominantly pyroxenitic character of the rocks, water pressure rose toward the late stages of crystallization as indicated by the presence of phlogopite and occasionally both amphibole and zeolite. Shrinkage of the leucite stability field attendant upon this rise in left the liquid that was crystallizing nepheline and leucite stranded on the nepheline-alkali feldspar cotectic. Shrinkage occurred too rapidly for the liquid to remain at the reaction point of the system, and leucite, therefore, was not resorbed. The remaining liquid crystallized rapidly as flames of vermicular intergrowth of nepheline with potassium feldspar (composition Ne 24.0, Ks 45.9, Qz 30.1), a texture that might be attributable to supercooling. Silica-rich leucite compositions (Ks 68.8, Qz 31.2) decomposed to intergrowths of kalsilite with potassium feldspar but reaction kinetics, or possibly variations in throughout the intrusion, prevented the breakdown of leucite.  相似文献   

7.
Thermodynamic calculations, modified after Nicholls et al. (1971), which relate the activity of silica in a lava to the temperature and pressure conditions at which the lava could be in equilibrium with a mantle mineral assemblage, have been extended to H2O-bearing magmas by using published experimental data to derive the dependence of on the weight fraction of H2O dissolved in a magma. A petrogenetic grid has been calculated which gives the P-T conditions under which a magma with a given at its liquidus at 1 atm could equilibrate with a mantle mineral assemblage containing olivine (ol) and orthopyroxene (opx) for different amounts of H2O in the magma at its source. This grid is in good agreement with the results of experimental studies as summarized by Green (1971) and Brey and Green (1975). The results show that the pressure at which a given magma composition can equilibrate with ol + opx increases for increasing amounts of H2O dissolved in the magma at depth.In addition, experimental data have been used to calculate the effect of olivine crystallization and removal on the in the residual liquid to assess the effect of low-pressure differentiation on . The results show that if 20 % olivine is added to a basalt magma, its calculated pressure of equilibration with ol+opx increases by 4–5 kbar for a given temperature. The calculated effects of olivine removal and H2O addition on are reasonably consistent with the silicate mixing model of Burnham (1975).Thermodynamic calculations of this type may be useful for assessing the internal consistency of certain experimental data, and in extrapolating the results to other magma compositions. The application of these calculations to determining the possible depth of origin of natural lavas appears to be limited primarily by the difficulty in determining in a lava at its liquidus temperature.  相似文献   

8.
A model system for mineral facies in pelitic schists   总被引：5，自引：0，他引：5  
The system Na2O-K2O-Al2O2-SiO2-H2O contains many mineral phases of major importance in the diagenesis and metamorphism of shales and sandstones, as well as in felsic igneous rocks and their metamorphic derivatives. It is thus a useful model-system containing many of the key equilibria of concern in the genesis of such rocks. It is also a system for which extensive experimental and thermodynamic data are available.The discontinuous reactions among the phases quartz, albite, potassic feldspar, muscovite, paragonite, pyrophyllite, kaolinite, kyanite, andalusite, sillimanite, jadeite and analcime have therefore been used to construct a model system for mineral facies in pelitic rocks. There appear to be fiftynine possible facies types, separated by forty-one discontinuities, only thirtysix of which are readily observed in the field. The continuous reactions, involving rotations of tie-line and displacements of three-phase triangles in the NaAlO2-KAlO2-Al2O3 projection from SiO2-H2O, may be formulated using either an Na or K end-member reaction together with Na-K exchange reactions between coexisting white micas, alkali feldspars and analcimes. The general stoichiometric coefficients for all likely discontinuous reactions have been evaluated in terms of mol fractions of end-members. Available experimental data have been used to calibrate the discontinuous equilibria for the limiting conditions of = 0 and = 1. The (Na-K) facies types may be correlated with (Fe-Mg) facies types in pelitic rocks or with assemblages in mafic rocks.This paper is a revised and extended version of a paper entitled Mineral Facies in Pelitic Schists by J. B. Thompson, Jr., published in 1961 as part of a testimonial volume in honor of D. S. Korzhinskii (originally published in Russian with an English summary)  相似文献   

9.
  相似文献   

10.
The univariant reaction governing the upper stability of heulandite (CaAl2Si7O18·6H2O), heulandite=laumontite+3 quartz+2H2O (1), has been bracketed through reversal experiments at: 155±6° C, 1000 bar; 175±6° C, 1500 bar; and 180±8° C, 2000 bar. Reversals were established by determining the growth of one assemblage at the expense of the other, using both XRD and SEM studies. The standard molal entropy of heulandite is estimated to be 783.7±16 J mol–1 K–1 from the experimental brackets. Predicted standard molal Gibbs free energy and enthalpy of formation of heulandite are –9722.3±6.3 kJ mol–1 and –10524.3±9.6 kJ mol–1, respectively. The reaction (1), together with the reaction, stilbite=laumontite+3 quartz+3 H2O, defines an invariant point at which a third reaction, stilbite=heulandite+ H2O, meets. By combining the present experimental data with past work, this invariant point is located at approximately 600 bar and 140° C. Heulandite, which is stable between the stability fields of stilbite and laumontite, can occur only at pressures higher than that of the invariant point, for = P total.These results are consistent with natural parageneses in low-grade metamorphic rocks recrystallized in equilibrium with an aqueous phase in which is very close to unity.  相似文献   

11.
The Costabonne skarn complex was emplaced in the lower part of the Cambrian Canaveilles Formation (eastern Pyrenees) in contact with a Hercynian granitic stock. Skarns have developed from calcium-poor (<1% CaO) pelitic rocks. A zonation can be clearly seen: schists (Z0), biotite zone (Z1), amphibole zone (Z2), pyroxene zone (Z3), and garnet zone (Z4). Two superposed successions of transformations are observed: (1) muscovitefeldspar garnet and (2) biotiteamphibolepyroxene. Calculation of mass transfer indicates an important exchange of CaO and K2O and, in lesser amounts, Fe2O3, MgO and MnO. SiO2, Al2O3, FeO, TiO2, the heavy rare earths (HREE) and most of the trace elements remain constant; whereas the contents of Na2O, Rb, Sr, Ba, and the light rare earths elements (LREE) are reduced. According to fluid inclusion data and mineral compositions, the metasomatic fluid was mainly 0.99)$$ " align="middle" border="0"> with minor CO2, CH4, N2, H2, O2, H2S, HCl and HF. Ca, Na, and K were the most abundant cations. Temperature and pressure conditions are estimated to be at least 550° C and 1.7 to 2.0 kb, respectively. The totality of the observed transformations may be described in the system CaO-K2O-SiO2-Al2O3-MgO-H2O with the minerals quartz, muscovite, phlogopite, tremolite, diopside, grossular, K-feldspar, and anorthite. With CaO and K2O taken as perfectly mobile components, SiO2, Al2O3, and MgO as determining inert components and H2O as excess component, the reactions leading to the skarn formation can be represented in a diagram. The succession of zones is shown to take place with increasing CaO from the schist (Z0) up to the garnet zone (Z4). The nature of the feldspar (plagioclase or K-feldspar) depends on the value of relative to CaO.  相似文献   

12.
Ferric iron contents of coexisting ortho- and clinopyroxene from spinel lherzolite xenoliths were measured with Mössbauer spectroscopy and found to be significant. In orthopyroxene, the range in Fe3+/Fe is from 0.04 to 0.14; in clinopyroxene, the range is from 0.12 to 0.24. Reactions involving coexisting olivine, orthopyroxene, and clinopyroxene, where either the esseneite (CaFe3+ AlSiO6) or the acmite (NaFe3+Si2O6) component in the clinopyroxene is considered, are used to calculate oxygen fugacities. These oxygen fugacities agree well with those calculated with the olivine-orthopyroxene-spinel oxybarometer. Because these reactions do not involve garnet, spinel, or plagioclase, they may be applied to lherzolites to give internally-consistent oxygen fugacities across the pressure-dependent facies boundaries between plagioclase, spinel, and garnet lherzolite. Another application of this method is to predict the Fe3+/Fe in clinopyroxene coexisting with olivine and orthopyroxene given pressure, temperature, , and the compositions of the coexisting phases in either experimental or natural assemblages. At values of equal to those of the synthetic fayalite-magnetite-quartz buffer, for example, 15–35% of the iron in the clinopyroxenes from these xenoliths would be ferric. The simplifying assumption that all Fe is divalent in silicate phases at geologically — reasonable oxygen fugacities must be re-evaluated.  相似文献   

13.
Deerite, Fe 12 2+ Fe 6 3+ [Si12O40](OH)10, thus far known from ten localities in glaucophane schist terranes, was synthesized at water pressures of 20–25 kb and temperatures of 550–600 °C under the of the Ni/NiO buffer. The X-ray powder diagram, lattice constants and infrared spectrum of the synthetic phase are closely similar to those of the natural mineral. A solid solution series extends from this ferri-deerite end member to some 20 mole % of a hypothetical alumino-deerite, Fe 12 2+ Al 6 3+ [Si12O40](OH)10. The upper temperature breakdown of ferri-deerite to the assemblage ferrosilite +magnetite+quartz+water occurs at about 490 °C at 15 kb, and 610 °C at 25 kb fluid pressure for the of the Ni/NiO buffer. Extrapolation of these data to lower water pressures indicates that deerite can be a stable mineral only in very low-temperature, high-pressure environments.  相似文献   

14.
APL computer programs for the thermodynamic calculation of devolatilization and solid-solid equilibria operate using stored values for the molar volume and entropy of solids, the free energies of H2O and CO2, and the free energies of formation for 110 geologically-important phases. P-T-X CO 2 calculations of devolatilization equilibria can be made at pressures from 0.2 through 10 kb, and temperatures from 200 through 1,000° C. P-T-X calculations of solid-solid equilibria may be accomplished at pressures to 30 kb and temperatures to 1,000° C. Calculations can be extrapolations from experimental points, or direct calculations from thermochemical data alone. Options are available in these programs to consider effects of: real vs. ideal gas mixing, thermal expansion and compressibility, solid solution, fluid pressure differing from solid pressure, and uncertainties in high-temperature entropies.A collection of thermodynamic data programs accompanies the programs for calculating P-T-X CO 2 equilibria. Over a wide range of physical conditions, the data functions report free energies, entropies, fugacities of H2O and CO2, high temperature entropies of solids, and activities of components in H2O-CO2 mixtures.List of Symbols Activity of H2O and CO2 - Gf Free energy of formation of a phase from elements - Gr Free energy change of reaction - G r o Standard state free energy change of a reaction - Free energies of pure H2O and CO2 - H r o Standard state enthalpy change for a reaction - K Equilibrium constant - R Gas constant - S r o Standard state entropy change of reaction - S s o Standard state entropy change of solids in a reaction - Vs o Standard state volume change of a reaction - Vs o Standard state volume change of solids in a reaction - Mole fraction of H2O and CO2 - Activity coefficient of H2O and CO2  相似文献   

15.
One hundred years of rapakivi granite   总被引：31，自引：0，他引：31  
Summary Rapakivi granites, recently redefined as A-type granites showing rapakivi texture at least in the larger batholiths, occur on all continents and presumably represent the most voluminous continental silicic intraplate magmatism on Earth. Most of the rapakivi granites are Proterozoic (mainly 1.0 to 1.7 Ga) but also Archean (2.8 Ga) and Phanerozoic (0.05 to 0.4 Ga) are known. The magmatic association is bimodal comprising anorthosite to gabbro, diabase, minor Fe-enriched intermediate rocks, and monzonite, beside granite; mingling of silicic and mafic magmas is typical. Geochemically and otherwise, rapakivi granites show the characteristics of the Phanerozoic A-type granites, except that they encompass relatively few peralkaline rocks and that they may occur as very large (up to 40,000 km2) batholiths. Some of the rapakivi granite complexes host important Sn-polymetallic and Fe-Cu deposits.The rapakivi granites crystallized from relatively hot, restite-poor magmas at low (epizonal-subvolcanic) pressure, , and . Mineral assemblages are indicative of a multiphase crystallization history; the conspicuous mantling of the perthite ovoids with plagioclase can be explained by changes in magma composition and/or, P, T, and affecting the stabilities of feldspars. The isotopic composition of rapakivi granites is generally compatible with a lower crustal protolith. The latter could have been either a melt-depleted residue or otherwise relatively anhydrous igneous or metaigneous rock. Melting of the protolith commenced under vapor-absent conditions and was induced by heat from the contemporaneous mantle-derived mafic magmas. The widespread rapakivi granite magmatism in the Middle Proterozoic may have been related to the establishment of a major continental mass (supercontinent).
Einhundert jahre rapakivi-granit
Zusammenfassung Rapakivi-Granite sind A-Typ Granite mit Rapakivi Texturen, die zumindest in den größeren Batholiten zu erkennen sind. Sie kommen auf alien Kontinenten vor and stellen wahrscheinlich das umfangreichste Beispiel kontinentalen sauren Intraplate-Magmatismus dar. Die meisten Rapakivi-Granite sind proterozoisch (1.0 bis 1.7 Ga), jedoch sind auch archaische (2.8 Ga) and phanerozoische (0.05 bis 0.4 Ga) Beispiele bekannt. Die magmatische Assoziation ist bimodal and umfaßt Anorthosit bis Gabbro, Diabas, in kleinerem Umfang Fe-angereicherte intermediäre Gesteine and Monzonit, zusätzlich zu Granit. Das gemeinsame Auftreten von Silizium-reichen and mafischen Magmen ist typisch. Die geochemischen Charakteristika der Rapakivi-Granite entsprechen phanerozoischen A-Typ Graniten mit der Ausnahme, daß sie relativ wenige peralkaline Gesteine umfassen and dab sie als sehr große (bis zu 40.000 km2) Batholithe vorkommen können. Einige Rapakivi-Granite führen wichtige Zinn-polymetallische and Fe-Cu Lagerstätten.Die Rapakivi Granite kristallisierten aus einem relativ heißen, Restit-armen Magma bei niedrigem (epizonalem bis subvulkanischem) Druck, and . Mineralassoziationen weisen auf eine vielphasige Kristallisationsgeschichte hin; die auffallenden Umwachsungen von Perthit-Ovoiden mit Plagioklas konnen durch Änderungen in der Magmenzusammensetzung and/oder von P, T and erklärt wurden, die die Stabilitäten der Feldspate beeinflussen. Die Isotopen-Zusammensetzung der Rapakivi Granite entspricht im allgemeinen einem tieferen Krusten-Protolith. Der letztere kann entweder ein an Schmelze verarmtes Residuum oder auch ein relativ wasserarmes, magmatisches oder metamagmatisches Gestein gewesen sein. Schmelzen des Protoliths begann in Abwesenheit von volatilen Phasen and wurde durch Wärmezufuhr von gleichaltrigen mafischen Magmen, die aus dem Mantel stammen, herbeigeführt. Der weit verbreitete Rapakivi Granit-Magmatismus im mittleren Proterozoikum dürfte mit der Bildung eines Superkontinentes in Beziehung zu setzen sein.

With 11 figures  相似文献   

16.
Metasomatism and fluid flow in ductile fault zones   总被引：8，自引：0，他引：8  
Observed major element metasomatism in 5 amphibolite facies ductile fault zones can be explained as the inevitable consequence of aqueous fluid flow along normal temperature gradients under conditions of local chemical equilibrium. The metasomatism does not require the infiltration of chemically exotic fluids. Calculations suggest that metasomatized ductile fault zones are typically infiltrated by 105 moles H2O/cm2, fluid flow is in the direction of decreasing temperature, and fluids contain about 1.0 molal total chloride. Where available, stable isotopic alteration data confirm both flow direction and fluid fluxes calculated from major element metasomatism. The fluid fluxes inferred from metasomatism do not require large-scale fluid recirculation or mantle sources if significant lateral fluid flow occurs in the deep crust. Time-integrated fluid fluxes are combined with estimates of flow duration to constrain average flow rates and average permeabilities. Rocks in ductile fault zones are probably much more permeable during metasomatism (average permeabilities of 10-17 to 10-15 m2) than rocks normally are during regional metamorphism (10-21 to 10-18 m2). Estimated average fluid flow rates (3.5×10-3 to 0.35 m/yr) are insufficient, however, to significantly elevate ambient temperatures within ductile faults. Fluid flow in the direction of decreasing temperature may increase the ductility of silicate rocks by adding K to the rocks and thereby driving mica-forming reactions.  相似文献   

17.
Aenigmatite, sodic pyroxene and arfvedsonite occur as interstitial minerals in metaluminous to weakly peralkaline syenite patches in alkali dolerite, Morotu, Sakhalin. Aenigmatite is zoned from Ca, Al, Fe3+-rich cores to Ti, Na, Mn, Si-rich rims reflecting the main substitutions Fe2+Ti4+Fe3+, NaSiCaAl and Mn2+Fe2+. Aenigmatite replaces aegirine and ilmenite supporting the existence of a no-oxide field in — T space. In one case aenigmatite has apparently formed by reaction between ilmenite and arfvedsonite. Titanian aegirine (up to 3.0 wt% TiO2) and Fe-chlorite may replace aenigmatite. Sodic pyroxene occurs as zoned crystals with cores of aegirine-augite rimmed by aegirine and in turn by pale green aegirine containing 93 mol% NaFe3+Si2O6. Additional substitution of the type NaAlCaFe2+ is indicated by significant amounts (up to 6 mol%) of NaAlSi2O6. Arfvedsonite is zoned with rims enriched in Na, Fe and depleted in Ca which parallels the variation of these elements in the sodic pyroxenes.The high peralkalinity of the residual liquid from which the mafic phases formed resulted from the early crystallization of microperthite (which makes up the bulk of the syenites) leading to an increase in the Na2O/(Na2O+K2O) and (Na2O+K2O)/Al2O3 ratios of the remaining interstitial liquid which is also enriched in Ti, Fe, and Mn. Bulk composition of the melt, , temperature and volatile content were all important variables in determining the composition and stability of the peralkaline silicates. in the residual liquid appears to have been buffered by arfvedsonite-aegirine and later by the arfvedsonite-aenigmatite and aenigmatite-aegirine equilibria under conditions of a no-oxide field. An increase in , above that of the alkali buffer reactions, is inferred by an increase of Ti and Mn in aenigmatite rims. The latest postmagmatic vapour crystallization stage of the syenites is marked by extremely low which may have been facilitated by exsolution of a gas phase. Low is supported by the replacement of aenigmatite by titanian aegirine, and the formation of rare Ti-rich garnet with a very low (Ti4++Fe3+)/(Ti+Fe) ratio of 0.51, associated with leucoxene alteration of ilmenite.  相似文献   

18.
The Miocene-Pliocene Macusani volcanics, SE Peru, outcrop in three separate tectonic intermontane basins developed on a Paleozoic-Mesozoic volcano-sedimentary sequence. Several ignimbrite sheets are recognized and K-Ar dates record at least semi-continuous volcanic activity from 10 to 4 Ma in the Macusani field. The volcanics in the Macusani basin comprise crystal-rich (45% crystals) ash-flow tuffs and rare obsidians glasses, both with unusual mineralogy, similar to two-mica peraluminous leucogranites. The mineralogical assemblage (quartz, sanidine Or69–75, plagioclase, biotite, muscovite and andalusite (both coexisting in the entire volcanic field), sillimanite, schörl-rich tourmaline, cordierite-type phases, hercynitic spinel, fluor-apatite, ilmenite, monazite, zircon, niobian-rutile) is essentially constant throughout the entire Macusani field. Two distinct generations of plagioclase are recognized, viz. group I (An10–20) and group II (An30–45). Sillimanite forms abundant inclusions in nearly all phases and is earlier than andalusite which occurs as isolated phenocrysts. Biotite (Al-, Ti-, Fe- and F-rich) shows pronounced deficiencies in octahedral cations. Muscovite is also F-rich and displays limited biotitic and celadonitic substitutions. There is no systematic variation in mineral chemistry with stratigraphic position. The mineralogical data provide a basis for distinction between an early magmatic and a main magmatic stage. The early stage corresponds to the magmatic evolution at or near the source region and includes both restites and early phenocrysts. Some biotites (with textures of disequilibrium melting to Fe — Zn spinel), part of the sillimanite, apatite and monazite, possibly some tourmaline and cordierite-type phases are restites. However, the restite content of the magma was low (5 vol. % maximum). The group II plagioclase are interpreted as early phenocrysts. During this stage, temperatures were as high as 800° C, pressure was no more than 5–7.5 kbar, was intermediate between WM and QFM and was low. The biotite melting textures and the coexistence of restites and early phenocrysts imply fast heating rates in the source region. The transition between the early and the main magmatic stage was abrupt (andalusite crystallization in place of sillimanite, group I vs. group II plagioclases) and suggests rapid ascent of the magma from its source region. During the main crystallization stage, temperature was 650° C or lower at a pressure of 1.5–2 kbar. (calculated from equilibrium between muscovite, quartz, sanidine and andalusite) are around 1, suggesting conditions close to H2O-saturation. f HF is around 1 bar but the ratios are significantly different between samples. ranges between 138 and 225 bar. This study shows that felsic, strongly peraluminous, leucogranitic magmas having andalusite and muscovite phenocrysts may be generated under H2O-undersaturated conditions.CRPG Contribution n 769  相似文献   

19.
Garnet-pyroxene skarns were formed 90 m.y. B.P. in the Osgood Mountains at or near contacts of grandiorite with calcareous rocks of the Cambrian Preble Formation. The metasomatic replacement followed contact metamorphic recrystallization of the Preble. The sources, temperature, and variation in H2O/CO2 ratios of the metasomatic fluid are interpreted from 269 analyses of oxygen, carbon, hydrogen, and sulfur isotopes in whole rocks, minerals and inclusion fluids.Skarns formed in three mineralogical stages. Oxygen isotope data indicate that temperatures during the crystallization of garnet, pyroxene and wollastonite (Stage I) were least 550 ° C, and that the metasomatic fluid had an 0.035 in the massive skarns, and 0.12 in vein skarns up to 3 cm thick. Pore fluids in isotopic equilibrium with garnet in calc-silicate metamorphic rocks, on the other hand, had 0.15.The metasomatic fluids of Stage I were derived primarily from the crystallizing magma. The isotopic composition of magmatic water was 18O =+9.0, D= –30 to –45. Oxygen isotope temperatures of greater than 620 ° C were determined for the granodiorite. Isotopic and chemical equilibria between mineral surfaces and the metasomatic fluid were approached simultaneously in parts of the skarn several meters or more apart, while isotopic and chemical disequilibria (i.e. zoning) have been preserved between 20 to 40 m-thick zones in grandite garnet. More Fe-, or andradite-rich garnet crystallized in more H2O-rich C-O-H fluids ( 0.01) than present with grossularite-rich garnet ( 0.035).Stage II was marked by the replacement of garnet and pyroxene by quartz, amphibole, plagioclase, epidote, magnetite, and calcite. Many of the replacement reactions took place over a relatively narrow range in temperature (480–550 ° C), as indicated by 18O fractionations between quartz and amphibole. Meteoric water comprised 20 to 50% of the metasomatic fluid during Stage II.Calcite was formed along with pyrite, minor pyrrhotite, and chalcopyrite during Stage III, although the crystallization of pyrite and calcite had begun earlier, during Stages I and II, respectively. Carbon and sulfur isotope compositions of calcite and pyrite indicate a magmatic source for most of the C and S in the metasomatic fluids of Stage III. By the end of Stage III, meteoric water constituted as much as 100% of the metasomatic fluid. Minerals from grandiorite and skarn do not show large depletions in 18O because the oxygen isotope composition of the metasomatic fluid was buffered by the calcareous wall rocks and the grandiorite.Meteoric water in the vicinity of the Osgood Mountains during the Late Crectaceous (18Ocale. –14.0, D = – 107) was slightly enriched in 18O and D relative to present-day meteoric water (18O = 15.9, D = – 117)  相似文献   

20.
The interdependence of the Fe(Mg)–1 (e.g., FeO-MgO in silicate melt; CaFeSi2O6-CaMgSi2O6 in pyroxene) and TiAl2(MgSi2)–1 exchange reactions between silicate melts and coexisting Ca-pyroxene has been examined. High-calcium clinopyroxenes were grown in 1 atmosphere melting and crystallization experiments on rock powders spanning the composition range tholeiite to melilitite (1,0922+Mg2+ exchange and suggest that at given values of extent of Fe(Mg)–1 substitution is strongly coupled with the TiAl2(MgSi2)–1 substitution in pyroxenes near the five-component space CaMg(Si2O6-CaFe(Si)2O6-CaTi(Al)2O6-CaFe(Al,Si)2O6-CaAl(Al,Si)2O6. The inferred stabilization of Ti in iron-rich relative to magnesium pyroxene is consistent with the operation of Fe2+Ti4+ intervalence charge transfer interactions (e.g., Rossman 1980) and observations on zoning in natural titanaugites (e.g., Tracy and Robinson 1977). Although the rims of some pyroxenes grown in some melting experiments exhibit prominent zoning in TiAl2(MgSi2)–1, the average values of inferred from the compositions of these pyroxenes, together with those of the relatively homogeneous pyroxenes produced in crystallization experiments, exhibit a 11 correlation with values of derived from the solution model of Ghiorso et al. (1983) with a standard error of 750 calories. The Ti contents of Ca-rich pyroxenes crystallizing from a wide range of natural silicate liquids can therefore be predicted.  相似文献   

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