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1.
Pressure solution and vein formation often occur simultaneously in shear zones during the deformation of sedimentary rocks. The mineralogical and chemical variations around a typical example of an en echelon zone of quartz veins from north Cornwall are discussed in detail. Solution of quartz is confined to the shear zone and occurs along discrete surfaces. Accumulation of insoluble minerals along these surfaces gives rise to spaced pressure solution cleavage. Petrographic data show that during pressure solution the breakdown of felspar and epidote results in the crystallisation of clay mineral, quartz and siderite. Redistribution of silica within the shear zone by pressure solution does not account for all the quartz in the veins, or for the observed increased concentration of iron and calcium. It is concluded that material was introduced from an external source into the shear zone.  相似文献   

2.
Abstract. The Batu Hijau porphyry Cu‐Au deposit, Sumbawa Island, Indonesia, is associated with a tonalitic intrusive complex. The temperature‐pressure condition of mineralization at the Batu Hijau deposit is discussed on the basis of fluid inclusion microthermometry. Then, the initial Cu‐Fe sulfide mineral assemblage is discussed. Bornite and chalcopyrite are major copper ore minerals associated with quartz veinlets. The quartz veinlets have been classified into ‘A’ veinlets associated with bornite, digenite, chalcocite and chalcopyrite, ‘B’ veinlets having chalcopyrite bornite along vuggy center‐line, rare ‘C’ chalcopyrite‐quartz veinlets, and late ‘D’ veinlets consisting of massive pyrite and quartz (Clode et al., 1999). Copper and gold mineralization is associated with abundant ‘A’ quartz veinlets. Abundant fluid inclusions are found in veinlet quartz consisting mainly of gas‐rich inclusions and polyphase inclusions throughout the veinlet types. The hydrothermal activity occurred in temperature‐pressure conditions of aqueous fluid immiscibility into hypersaline brine and dilute vapor. The halite dissolution (Tm[halite]) and liquid‐vapor homogenization (Th) temperatures of the polyphase inclusions in veinlet quartz range from 270 to 472d?C and from 280 to 454d?C, respectively. The estimated salinity ranges from 36 to 47 wt% (NaCl equiv.). The apparent pressures lower than 300 bars are estimated to have been along the liquid‐vapor‐halite curve for the fluid inclusions having the Th lower than the Tm that trapped the brine saturated with halite, or at slightly higher pressure relative to liquid‐vapor‐halite curve for the fluid inclusions having the Th higher than the Tm that trapped the brine unsaturated with halite. The actual temperature and pressure during the hydrothermal activity at the Batu Hijau deposit are estimated to have been around 300d?C and 50 bars. At such temperature‐pressure conditions, the principal and initial Cu‐Fe sulfide mineral assemblages are thought to be chalcopyrite + bornite solid solution (bnss) for the chalcopyrite‐bearing assemblage, and chalcocite‐digenite solid solution and bnss for the chalcopyrite‐free assemblage.  相似文献   

3.
Grain-to-grain and stylolitic solution structures in two central Appalachian Siluro–Devonian limestone macroscale folds contain one of four distinct mineral assemblages that are characterized by the dominant iron-phase mineral present: (1) chlorite±illite±pyrite±calcite±quartz±TiO2±goethite, (2) chlorite±illite±pyrite altered to iron oxide/hydroxide±calcite ±quartz±TiO2, (3) chlorite±illite±magnetite±calcite±quartz, and (4) chlorite±illite±goethite±calcite±quartz±TiO2. Optical reflectance microscopy and SEM–EDS was used to characterize the mineralogy and mineral morphology of these structures. Geochemical modeling was used to constrain the conditions of formation and preservation.The primary control on solution structure mineral assemblage was the redox conditions present in the solution structures during burial and deformation. The redox conditions on the microscale may have been controlled by the local fluid chemistry and the presence–absence of hydrocarbons and organic acids within the formation fluids, and the influx of externally derived fluids by fracture formation during the folding process. The wide variation in mineralogy of the solution structures shows that they were ‘chemical factories’ where a variety of chemical reactions took place during rock dissolution. In particular, the formation of authigenic magnetite in solution structures has significant implications for paleomagnetic applications, and use of anisotropy of anhysteretic remanent magnetization and anisotropy of magnetic susceptibility fabrics.  相似文献   

4.
Alastair Beach 《Lithos》1979,12(1):51-58
The most widespread record that terrigenous sedimentary rocks have deformed by a pressure solution mechanism is seen in the development of spaced cleavages and transposition structures under conditions of low grade metamorphism. Such structures are most common in immature sandstones and siltstones. Mineral reactions, involving modification of detrital grains and diagenetic minerals, and forming a logical extension to diagenetic processes, are an integral part of the deformation mechanism, and the cleavage stripes represent accumulations not just of inert particles, but mostly of newly crystallized micas, the products of these reactions. The mechanism of deformation by pressure solution is now seen to involve mmetamorphic reactions, change in volume of solid phases during reaction, removal of some silica from the rock, rearrangement of reaction products to produce fabrics, solution of some detrital grains in cleavage stripes.Formal reactions have been written to describe the alteration of detrital felspar and epidote to white mica, the modification of greywacke matrix to white mica, and the transformation of diagenetic chlorite to white mica, all of which are observed to occur during formation of the pressure solution cleavages. These reactions emphasize the importance of metamorphic processes during pressure solution deformation, suggest that pressure solution may involve removal of silica released as a product of the reactions, indicate that the pH of the aqueous phase may be buffered to a level that silica solubility is increased, involve a volume reduction that contributes to the overall shortening during deformation, and also involve dehydration, the large scale circulation of released water possibly being important to the removal and redistribution of silica during pressure solution.  相似文献   

5.
“Pressure solution”, frequently found in clay-rich sandstone, is characterized by enhanced quartz dissolution at inter-grain contacts. The origin of pressure solution and many other related dissolution processes remains elusive. Using an Electrochemical Surface Forces Apparatus we visualized and measured the dissolution of silica glass surfaces close to an electrode surface. The dissolution rates correlate quantitatively with the electrode potential via the Butler-Volmer equation for corrosion. Our experimental results demonstrate that at low temperature, apparent pressure solution and many other mineral dissolution phenomena can be driven by electrochemical processes rather than a pressure-driven process. This finding highlights the role of electrochemical surface potentials in dissolution phenomena at dissimilar material interfaces, and provides new perspectives on pressure solution in particular and a new theoretical basis for predictive control of dissolution phenomena in general.  相似文献   

6.
Whereas much petrographic evidence for pressure solution, in sedimentary rocks has been accumulated since Sorby's work, its thermodynamic justification has never been clearly established, and has been challenged by some authors. Difficulties disappear when it is recognized that in the most general case migration of chemical components proceeds down chemical-potential gradients rather than down concentration gradients. Along a grain contact a chemical-potential gradient is produced by variations in contact pressure and by local variations in Helmholtz energy of the solid. For example, in a sand made up of even-sized spherical grains buried 500 m, the ratio of the diameter (D) of the grains to that of a spherical elastic contact circle (a) is D/a ～- 26. The chemical potential at the center of such an elastic contact is ～- 14kcal mol?1 higher than in surrounding pore water saturated with respect to quartz. For comparison, at a temperature of 30°C, saturation with respect to amorphous silica rather than quartz raises the chemical potential by only 1.6 kcal mol?1. If the diameter of the contact circle has enlarged to e.g. a = D/5, the chemical potential at its center is still 0.5 kcal mol ?1 greater than that of free quartz under hydrostatic pressure. The corresponding potential gradients are the driving force of pressure solution. The concept of pressure solution thus does not contradict any thermodynamic principle; in particular, it does not require that the chemical component of the solid have a smaller partial volume in solution than in the solid state. Petrographic and experimental evidence can therefore be accepted without reservation.  相似文献   

7.
The process of pressure solution is defined as the dissolution of materials under high stress at grain-to-grain contacts and precipitation at interfaces under low stress. The kinetics of this process are still poorly understood mainly because of the large timescales involved. In this research, the Surface Forces Apparatus (SFA) technique was coupled with an optical interference technique for in situ visualization of the nanoscale deformations and thickness changes. The SFA was used to measure the forces (or pressures) and distances between two solid surfaces pressed together with a thin film between them. Using the SFA, combined with geological observations, we are studying the short-range colloidal forces between surfaces of mica and silica at the nanoscale such as van der Waals, electrostatic, and hydration forces.

This study involves two cases, the symmetric case of mica in contact with mica and the asymmetric case of a quartz surface in contact with mica. Our results reveal highly subtle effects depending on the nature and concentration of the counterions present in the solution either of Na+, Ca2+, or mixtures of these ions, as well as on the pH. For the symmetric case, the equilibrium interactions of force F or pressure P versus fluid film thickness T have been measured between the mica surfaces across aqueous films in the thickness range from T = 25 Å down to contact separations around T = 0 Å, and depend on the solution conditions and applied lithostatic pressure. Measurements have also been made of the rates of diffusion of ions through such ultra-thin films and on the precipitation and growth of ionic crystallite layers on the surfaces. Our results show that the diffusion coefficient of hydrated sodium is two orders of magnitude lower than the diffusion of water into mica–mica cleavage and a factor of 40 lower than the coefficient of sodium ions in bulk water.

For the asymmetric case, the dissolution of the quartz surface was observed to be dependent on the interfacial fluid composition and pH, the externally applied ‘lithostatic’ pressure, and the type of crystalline structure exposed to the mica surface. Our experiments also show that there is an initial stage after fresh solution is added in which the spacing between the surfaces increases, however, the thickness started decreasing steadily after approximately 4 h of exposure independently of the crystallinity of the quartz surface. For a particular set of conditions, the process eventually slows down and reaches equilibrium after some time, but a further increase in pressure restarts the dissolution process. This is also true for the addition of fresh interfacial solution during the experiment after a period of thickness fluctuation. These results are consistent with the observation that pressure solution of quartz is greatly enhanced with the presence of mica.  相似文献   


8.
The enhancement of dissolution of quartz under the influence of clays has been recognized in sandstones for many years. It is well known that a grain of quartz in contact with a clay flake dissolves faster than when in contact with another grain of quartz. This phenomenon promotes silica transfer during the diagenesis of sandstones and is responsible of deformation and porosity variations. Here we make an attempt to explain the process of this rock deformation using a pressure solution mechanism.

The model of water film diffusion assumes that matter is dissolved inside the contact between two grains. The resulting solutes are transported to the pore fluid through diffusion along an adsorbed water film. Between two micas, this trapped film is thicker than between two grains of quartz. As a consequence diffusion is easier and the rate of pressure solution faster.

Experiments on pressure solution show that diffusion controls the mechanism at great depth whereas a model based on natural mica indentation indicates that kinetics is the limiting process through the precipitation rate of quartz at low depth, thus temperature is a crucial parameter. There should be a transition between thermally controlled rate and diffusion limited evolution.  相似文献   


9.
The uptake of water in quartz at 1.5 GPa total pressure, 1173 K and high water fugacity, over times up to 24 h, has been investigated using a newly developed assembly to prevent microcracking. It is found that the uptake is small, and below the detectability of the presently used technique of infrared spectroscopy and serial sectioning. This observation reflects either a low value for the diffusivity or the solubility or a combination of both, and is in agreement with the observations of Kronenberg et al. (1986) and Rovetta et al. (1986). It brings into question the interpretation of the early experiments on water weakening by Griggs and Blacic (1964) and the recent estimates of the solubility and diffusivity by Mackwell and Paterson (1985). Rults of a combined T.E.M., light-scattering and infrared-spectroscopy investigation of ‘wet’ synthetic quartz before and after heating at 0.1, 300 and 1500 MPa total pressure and 1173 K, strongly suggest that the water in ‘wet’ quartz is mainly in the form of H2O in inclusions, consistent with the solubility being low, possibly less than 100 H/106Si. From these observations, water-containing inclusions appear to play a major role in the plasticity of quartz, while any role of water in solid solution remains to be clarified.  相似文献   

10.
Petrographic and SEM observations on 478 samples of six quartzose sandstones provide a data base that can be used to evaluate the role of intergranular pressure solution (IPS) in sandstone diagenesis and to constrain predictive models of the pressure solution process. SEM examination of grain contacts that have experienced pressure solution suggests that IPS occurs at the interior portions of contacts where the greatest stress is concentrated and that granulation of quartz grains at points of contact may contribute to the process. The chemical compaction fabrics that result from IPS suggest that the process is most commonly induced by effective lithostatic stress and that the resulting strain is uniaxial.Numerous geological variables influence IPS. Grain size exerts a fundamental influence, with finer grained samples experiencing more IPS than coarser grained samples. On both local and regional scales, IPS is inhibited by poor sorting, an abundance of ductile grains, the presence of “shallow” cement, slow rates of shallow burial, and overpressured conditions. In contrast, IPS is enhanced by the presence of illite grain coatings, increased maximum burial depth, rapid rates of shallow burial, longer times spent at great depths, higher temperatures, and high volumes and rates of fluid flow.Silica budgets indicate that some of the analyzed sandstones approximate mass balance whereas others have exported silica. Calculations of fluid flow requirements indicate that advanced stages of IPS are favored by high volume, high velocity fluid flow. Such flow can occur as a result of uplift of basin margins, which is typical of foreland and intractonic basins.  相似文献   

11.
Batch and flow-through experiments were performed on quartz–feldspar granular aggregates at hydrothermal conditions (up to ≈150 °C, up to 5 MPa effective pressure, and near-neutral pH) for up to 141 days. The effect of dissolution–precipitation reactions on the surface morphology of the mineral grains was investigated. The starting materials as well as the solids and fluids resulting from the experiments were characterized using BET, energy dispersive X-ray spectroscopy, electron microprobe analysis, inductively coupled plasma-optical emission spectroscopy, scanning electron microscopy, transmission electron microscopy, X-ray powder diffraction, and X-ray fluorescence spectroscopy. The electrical conductivity of fluid samples was used as a proxy for the evolution of the fluid composition in the experiments. The chemical analyses of the fluids in combination with hydrogeochemical simulations with PHREEQC suggested the precipitation of Al–Si-bearing solid phases. Electron microscopy confirmed the formation of secondary amorphous Al–Si-bearing solid phases. The microscopic observations are consistent with a process of stoichiometric dissolution of the mineral grains, transport of dissolved ions in the fluid phase, and spatially coupled precipitation of sub-μm sized amorphous particles on mineral surfaces. These findings shed light onto early stages of diagenesis of quartz–feldspar sands and indicate that amorphous phases may be precursors for the formation of crystalline phases, for example, clay minerals.  相似文献   

12.
Rocks from two parts of the Ultradauphinois Zone of the external French Alps have been examined, and the mechanisms by which they were deformed have been assessed from petrographic data. Jurassic and Triassic limestones deformed by pressure solution, dissolving non-ferroan-calcite and precipitating ferroan-calcite. Calcite pressure shadows are usually less elliptical in shape than pyrite pressure shadows, and grain boundary sliding is therefore thought to have played a significant role. Eocene rocks deformed by a variety of mechanisms. Limestones show mylonitic textures, whereas limestone conglomerates with a quartz-sandstone matrix deformed by pressure solution of calcite and grain boundary sliding of quartz. A model for enhanced diffusion of silica along mica seams is proposed to account for planar quartz-mica boundaries. Greywackes deformed by incongruent pressure solution, involving the metamorphic reaction of feldspar to mica and quartz, coupled with the replacement of feldspar by calcite.  相似文献   

13.
Crystallization experiments were performed on quartz diorite (~55 wt.% SiO2, 3.1–8.4 wt.% MgO) from the G?siniec Intrusion (Bohemian Massif, SW Poland) at 1?2 kbar, 750–850°C, various mole fractions of water and with fO2 buffered by the NNO buffer. The two natural quartz diorites (leucocratic poikilitic quartz diorite - ‘LPD’ and melanocratic quartz diorite - ‘MD’) differ in whole rock and mineral composition with MD being richer in MgO and poorer in CaO than LPD, probably due to accumulation of mafic minerals or melt removal in MD. LPD represents melt composition and is used to reconstruct crystallization conditions in the G?siniec Intrusion. The crystallization history of LPD magma, deduced from experimental and natural mineral compositions, includes a higher pressure stage probably followed by emplacement at ~2 kbar of partly crystallized magma at temperatures ~850?800°C and quick cooling. The mineral assemblage present in LPD requires water contents in the magma of at least 5 wt% and oxygen fugacity below that controlled by the NNO buffer. The compositions of mafic minerals in the MD composition were equilibrated at temperatures below 775°C and at subsolidus conditions. The equilibration was probably due to the reaction between water-rich, oxidizing residual melt and the cumulatic-restitic mineral assemblage. MD is characterized by occurrence of the euhedral cummingtonite and increasing anorthite content in the rims of plagioclase. A similar reaction was reproduced experimentally in both LPD and MD compositions indicating that cummingtonite may be a late magmatic phase in quartz dioritic systems, crystallizing very close to solidus and only from water saturated magma.  相似文献   

14.
Porphyroblastic schists in the thermal aureole of the Victor Harbor Granite at Petrel Cove, in the southern Adelaide Fold Belt, South Australia, preserve a record of sequential cordierite, andalusite, staurolite, fibrolite, chlorite and muscovite growth (along with biotite+plagioclase+quartz+ilmenite) during progressive deformation. A P–T pseudo‐section appropriate to biotite‐saturated assemblages in KFMASH shows that the sequence of mineral reactions records increasing pressure of at least 1 kbar (from c. 3 to c. 4 kbar) during cooling from around 580 °C. Heating at pressures below c. 3 kbar is inferred for growth of early formed cordierite porphyroblasts, and is attributed in part to the thermal effects of granite emplacement, while the pressure increase is attributed to tectonic burial accruing from ongoing deformation. The ‘anticlockwise’P–T path is consistent with convergent deformation being focussed as a consequence of heating, as to be expected for a lithospheric rheology that is strongly temperature dependent.  相似文献   

15.
A mass transfer model of bauxite formation   总被引：1，自引：0，他引：1  
The formation of bauxite due to weathering of a granitic protolith has been simulated by means of a one-dimensional flow and reaction model based on the mass transfer principle. The model couples mineral dissolution and precipitation reactions, speciation in solution, and advective solute transport in a porous medium. A very important aspect of the modeling study is the use of mineral reaction rates determined experimentally in the laboratory. The important effects of solution saturation state and pH have been incorporated into the kinetic rate laws governing the heterogeneous reactions. The values of these parameters have been obtained from the scientific literature to guarantee that realistic reaction rates are used in the simulations. Albite and quartz are the minerals that make up the parent rock in the model. Gibbsite, kaolinite, and a Na-mica (as a surrogate for smectite) are the secondary minerals that have been taken into account. Long-term simulations (>1 Ma) have been run, and the formation of a bauxitic profile, with an upper gibbsite-rich and a lower kaolinite-rich zone, is predicted. In early stages of the process (up to a few hundreds of thousands of years), both gibbsite and kaolinite precipitate directly from solution as a consequence of albite dissolution. In later stages, the bulk of gibbsite precipitation derives from the incongruent dissolution of kaolinite, while kaolinite precipitation is still caused by the dissolution of albite. This is also reflected by the formation of two reaction fronts in the profile. These results are compared with weathering sequences from the Los Pijiguaos bauxite deposit, Venezuela. The overlap between the gibbsite and kaolinite zones and the replacement of kaolinite by gibbsite are consistent with model calculations. Mechanical denudation has to be called upon to explain the limited thicknesses of the weathering profiles in the field. The role of mechanical erosion is supported by the presence of microsedimentary structures in the bauxite and the balance between dissolved and suspended loads in the streams draining the area.  相似文献   

16.
Abstract Layer-parallel (i.e. parallel to foliation or bedding) vein formation in the graywackes and pelites of the Quetico Metasedimentary Belt occurred during synchronous prograde metamorphism and regional (D2) compression. In a traverse across metasediments which change in metamorphic grade from greenschist to upper amphibolite (migmatite) facies, layer-parallel veins show the following trends: (1) an increase in thickness and internal complexity, the latter due to successive boudinage; (2) low-grade veins are parallel to planes of anisotropy due to the original sedimentary fabric of the host rocks, but at higher grades other sites are also used and (3) a systematic increase in plagioclase/quartz ratio in the veins towards higher grade, adjacent mafic selvedges first exhibit quartz depletion then, in the amphibolite facies, plagioclase depletion. Mineralogical zoning is often preserved in a single vein, older parts are more quartz-rich than younger. Mass balance calculations and whole-rock geochemistry based on veins, mafic selvedges and country rock are consistent with a closedsystem subsolidus segregation origin. The layerparallel veins are syntectonic, and migration of the mobile components required to form their mineralogy is a stress-induced mass transfer. The source of these components appears to be dominantly pressure solution of the same minerals in the host rocks, although metamorphic reactions may also have contributed. Veins nucleated first at those sites where initial sedimentary heterogeneites, such as fine-scale graded bedding, provided gradients of normal stress across grain boundaries, and hence of chemical potential, necessary to drive the subsolidus segregation process. The earliest veins are thus parallel to bedding. Later, nucleation of the veins could also occur along more randomly distributed sites within the metasediments, and these veins grew parallel to the schistosity rather than bedding, if the two were distinct. Once formed, the veins themselves, which are more competent than the surrounding rock, provide the stress heterogeneity required for their further growth. The increasing plagioclase/quartz ratio in the veins may be due to a temperature dependent increase in plagioclase component mobility relative to quartz. Alternatively, the increasing transfer distances for silica, resulting from prior quartz depletion in the inner parts of the mafic selvedge, may increase the relative mobility of plagioclase component.  相似文献   

17.
Stress affects chemical processes on all scales in the Earth but the magnitude of its effect is debated. Here, I give a new synthesis of the theory that describes the effects of stress on chemistry, elaborating upon work in Materials Science which is built from fundamental thermodynamic laws, and show its significance in Earth Science. There are separate but compatible relationships describing what happens (1) at interfaces and (2) within grains. (1) The main chemical effects of stress in the Earth are due to variations in normal stress along grain interfaces and between interfaces with different orientations. For reactions involving diffusion these variations give effects on mineral stability broadly equivalent to pressure changes of (molar volume)/(molar volume change during reaction) × (stress variation). The volume ratio is generally large and so the effects of normal stress variations are always important since all stressed rocks have interfaces supporting different normal stresses. There is no global chemical equilibrium in a stressed system, so reaction kinetics contribute to ongoing evolution until stresses relax: this evolution can include deformation by diffusion creep and pressure solution, possibly with new mineral growth. These effects are relevant for predicting the conditions for reactions involving fluids, such as serpentinite formation and breakdown (relevant for the Earth's volatile cycles) and for other reactions such as ringwoodite breakdown (relevant for understanding the 660 km mantle discontinuity). (2) Within stressed solid solution grains it is not possible to define chemical potentials of all chemical components since one has to be specified as “immobile.” The chemical potential of a “mobile” component such as an exchange vector can be defined. It depends on the “partial molar strain,” a second rank tensor defining the variation in unit cell geometry with composition. In cubic crystals the partial molar strain is isotropic and the chemical potential of a mobile component depends on mean stress. In other crystal systems the partial molar strain is anisotropic and the chemical potential depends on a “weighted” mean stress; orientation as well as magnitude of stress has an influence. I propose “chemical palaeopiezometry”—the possibility of measuring past stress levels via chemistry. Examples show that stress variations in hundreds of MPa to GPa are required to produce 2% variations in composition but high stresses and/or precise chemical analyses will allow this proposal to be tested. High stresses around inclusions and dislocations could be targeted. So, the weighted mean stress inside grains has an effect which is relatively minor although potentially valuable in explaining chemical variations; the normal stress at interfaces plays the main role in chemical processes and its effects are of significant magnitude.  相似文献   

18.
Conspicuous, gently inclined, lenticular quartz–carbonate veins with fibre-textured infills dissect the steep, gold-bearing quartz veins in the Dolgellau Gold-Belt. Similar quartz veins fill the necks of boudin-like structures affecting the main gold-bearing veins at Clogau mine. They also dissect the post-mineralization ENE–WSW ‘Clogau Stone’ dykes. The uniformly oriented regional cleavage shows marked deflection around the gently inclined quartz veins. These late quartz veins were emplaced whilst the mudstones of the Clogau Formation, which host the steep gold-bearing quartz veins, were undergoing ductile deformation. The stretching involved in the late vein and boudin development requires these structures to be contemporaneous with some stage in the development of the regional sub-vertical cleavage and upright fold system. The earlier gold-bearing veins show evidence of brittle fracture and still retain some drusy space-filling textures. Cleavage is deflected adjacent to these early veins and in breccia clasts within the veins. The rare minor folds seen in the gold-bearing quartz veins have axial planar cleavages. It is concluded that the gold-bearing veins pre-date cleavage development. Thus they were forming when large amounts of water were still available in the sedimentary sequence, removing the severe source and transport problems that are implicit in the previous view that the veins were post-tectonic. Copyright © 1999 John Wiley & Sons, Ltd.  相似文献   

19.
In metabasites from the high‐grade metamorphic Kimi Complex of the Greek Rhodope, lamellae of quartz and amphibole were observed together with either rutile or titanite precipitates in the cores of clinopyroxene that underwent a prolonged exhumation history from eclogite via granulite and amphibolite facies conditions. Lamellae are crystallographically oriented along clinopyroxene cleavage planes (010) and interpreted as the result of precipitation during a two‐step intracrystalline compositional adjustment from an omphacite‐ to a Ca‐Tschermak‐rich clinopyroxene and finally to diopside. Even though retrograde diffusion profiles develop in clinopyroxene, the diffusion rates of highly charged ions like Si4+, Al3+and Ti4+are too slow, so precipitates rich in Si4+ (quartz), Al3+(amphibole) and Ti4+(rutile or titanite) form as viable kinetic alternatives. These precipitation reactions are not possible isochemically, and additional exchange of ions with the matrix is required for precipitation to occur. This exchange of mainly rapidly diffusing low‐charge ions is postulated to proceed by bulk diffusion (self‐diffusion) and does not require special pathways or fluid, even though these may play an additional role during metamorphism. This hitherto undescribed process of precipitation made possible by diffusional exchange with the matrix through an intact host crystal lattice is termed here as ‘open system precipitation’ (OSP). No prior Ca‐Eskola‐rich (ultrahigh‐pressure, UHP) composition of omphacite is required to explain the observed precipitates. It is proposed that many precipitation phenomena that were hard to explain in a closed‐system scenario can now be explained more readily by OSP. Calculation of an original solid solution composition, as in an UHP phase, from precipitate and host mineral analyses becomes imprecise to the degree that bulk diffusion and hence OSP have been important.  相似文献   

20.
黄骅坳陷三马地区中-深部储层成岩作用及主控因素分析   总被引：12，自引：2，他引：12  
黄骅坳陷三马地区储集岩样品的显微特征及成岩矿物的组合关系分析结果表明，三马地区下第三系中深层储层主要处于晚成岩A期，成岩现象包括石英、长石的次生加大、碳酸盐矿物胶结作用、矿物交代作用、溶解作用和粘土矿物转化作用等。其中石英次生加大于2700m左右开始出现，随埋深增大，石英增生加强；长石次生加大现象不十分普遍；碳酸盐胶结作用包括早期自生泥晶方解石胶结作用、连晶方解石和晚期白云石(或铁方解石)的胶结作用。在扫描电镜下可见到方解石与含铁方解石集合体充填在粒间孔隙中或与石英、钠长石及粘土矿物共生，白云岩多呈菱形粒状分布于粒间；常见的交代现象主要有方解石交代长石、石英及粘土矿物，粘土矿物交代长石、石英等；溶解作用主要有长石的溶解、碳酸盐颗粒的溶解和方解石胶结物的溶解等，粘土矿物的转化主要为蒙脱石、高岭石向伊利石(或绿泥石)转化。还讨论了储层岩相、岩性特征、孔隙水中有机酸含量、早期方解石的充填、烃类早期注入等因素对储层成岩演化的控制作用。  相似文献   

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