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1.
In this research, the possibility of replacing different portions of the normally used aggregate by acidic rocks was investigated.
These rock types outcrop at the northern part of Eastern Desert, southwest Ras Gharib area where large quantities of good
quality acidic rocks are available their. Portland cement concrete is a composite material made up of the hydrated cement
matrix, fine aggregate and coarse aggregate. The scanning electron microscope equipped with an energy dispersive X-ray analysis
system (EDX) has been applied to investigate several aspects of Portland cement concrete microstructure. The topics investigated
so far include the influence of aggregate composition on the development of the cement paste-aggregate interface and the formation
of calcium silicate hydrate CSH/calcium silicate aluminate CSA formation. The silicate gel coated the aggregates in the concrete
paste and crystallized into well defined needle like shape, cotton shape as well as euhedral to subhedral crystals of silicate/alumiante
and ettringite minerals with free lime librated from the hydrolysis process. The free lime can react again with the aggregates
leading to the formation of cementing materials which increase strength and durability of the concrete paste by increasing
the interfacial bonds between the used aggregates. 相似文献
2.
Samples of pyroclastic rocks from Abakaliki area (Nigeria) were subjected to geological and geochemical tests to determine the suitability and durability of the rocks as concrete aggregate. Petrographic analysis shows fine-grained texture and predominance of plagioclase (21–60 %) and shaley-muddy lithic fragment, while geochemical analysis classifies the rocks as alkaline. Analysis indicates that the pyroclastics would likely perform marginally well as concrete aggregates, especially in heavy Portland cement concrete and bituminous concrete. This is due to appreciably high values of natural moisture content, low bulk density, relative density and specific gravity, which suggests low durability, high voids and less aggregate absorption in concrete and bitumen mixes. The rocks are rated as moderate to high strength material on the basis of their unconfined compressive strength values, but are very likely to have low durability as buttressed by poor sulphate soundness test results, probably due to high amount of weak minerals. Analyses reveal that the Abakaliki Pyroclastics are not completely satisfactory as concrete aggregates source, despite their origin, texture, strength and economic availability. Hence, caution is required when they are used in concrete projects. 相似文献
3.
Ezz El Din Abdel Hakim Khalaf 《Arabian Journal of Geosciences》2014,7(7):2603-2624
Wadi Queih basin hosts a ～2,500-m thick Neoproterozoic volcanoclastic successions that unconformably lie over the oldest Precambrian basement. These successions were deposited in alluvial fan, fluviatile, lacustrine, and aeolian depositional environments. Diagenetic minerals from these volcaniclastic successions were studied by X-ray diffractometry, scanning electron microscopy, and analytical electron microscopy. The diagenetic processes recognized include mechanical compaction, cementation, and dissolution. Based on the framework grain–cement relationships, precipitation of the early calcite cement was either accompanied or followed by the development of part of the pore-lining and pore-filling clay cements. Secondary porosity development occurred due to partial to complete dissolution of early calcite cement and feldspar grains. In addition to calcite, several different clay minerals including kaolinite, illite, and chlorite with minor smectite occur as pore-filling and pore-lining cements. Chlorite coating grains helps to retain primary porosity by retarding the envelopment of quartz overgrowths. Clay minerals and their diagenetic assemblages has been distinguished between primary volcaniclastics directly produced by pyroclastic eruptions and epiclastic volcaniclastics derived from erosion of the pre-existing volcanic rocks. Phyllosilicates of the epiclastic rocks display wider compositional variations owing to wide variations in the mineralogical and chemical compositions of the parent material. Most of the phyllosilicates (kaolinite, illite, chlorite, mica, and smectite) are inherited minerals derived from the erosion of the volcanic basement complex, which had undergone hydrothermal alteration. Smectites of the epiclastic rocks are beidellite–montmorillonite derived from the altered volcanic materials of the sedimentary environment. Conversely, phyllosilicate minerals of the pyroclastic rocks are dominated by kaolinite, illite, and mica, which were formed by pedogenetic processes through the hydrothermal influence. 相似文献
4.
A. V. Bolonin A. V. Nikiforov D. A. Lykhin A. M. Sugorakova 《Geology of Ore Deposits》2009,51(1):17-32
The geological and mineralogical data on the Chailag-Khem F-Ba-Sr-REE occurrence in the Western Sayan Range, Russia, are discussed. The chemical compositions of rocks, ores, and minerals (ICP-MS, Link) are reported. The occurrence is localized in a tectonic crush zone composed of Cambrian quartz-sericite slates intruded by quartz syenite porphyry. Ore mineralization occurs as veins, cement of tectonic breccia, and metasomatic disseminations in host rocks. Massive ore consists of calcite, strontianite, and quartz; impregnations of euhedral fluorite, ankerite, and bastnaesite crystals; and fine-grained barite aggregate. Accessory minerals include parisite, synchysite, barytocelestine, sulfides, rutile, and uraninite. Late metasomatic calcite and strontianite segregations and veinlets are abundant. In genetic, mineralogical, and geochemical features, the Chailag-Khem occurrence is similar to the Late Mesozoic carbonatite deposits of Central Tuva, of which the Karasug Fe-F-Ba-Sr-REE deposit is the largest and best known. All carbonatite deposits and occurrences are located within a longitudinal zone transverse to the major tectonic elements of the region. 相似文献
5.
CO2矿物捕获能力的研究进展 总被引：2，自引：0，他引：2
全球碳存储的研究表明, CO2最稳定的存储方式是 CO2的矿物捕获, 即将 CO2注入到地下,使其以方解石、菱铁矿、白云石及片钠铝石等碳酸盐矿物的形式存在.适合 CO2矿物捕获的岩石类型主要有火山岩、砂岩和火山碎屑岩.分析了3种岩石类型的金属元素含量、金属元素的释放能力、与 CO2反应生成的矿物类型及对 CO2的捕获量,并比较了3种岩石类型对 CO2矿物捕获能力的差异.其中玄武岩等火山岩的金属离子含量高,但其孔隙空间有限,制约了成岩反应,且 CO2注入后具有逸散的风险;砂岩分布广泛,有足够的孔隙利于流体注入,但是金属离子含量相对较低,对 CO2的矿物捕获所需时间相对较长;火山碎屑岩则结合了前2种岩石类型在矿物捕获方面的优势,是一种理想的 CO2矿物捕获的岩石类型. 相似文献
6.
Geological and engineering characteristics of expansive soils and rocks in northern Oman 总被引：3，自引：0，他引：3
The geology and former climate of northern Oman favoured the formation of smectite clay minerals in certain materials which are implicated in ground heave problems. Investigations have shown that the smectite content of these expansive materials was developed in Oligocene, Miocene and Pliocene times. No evidence of a significant content of smectite was found in pre Eocene strata or in Quaternary strata, except for Desert Fill. It is shown that the main types of expansive materials in northern Oman are bentonitic mudstones, marls and silty mudstones, argillaceous dolomitic limestone, altered conglomerates and the desert fill derived from these. These swelling materials exist as impersistent bands within the bedrock Tertiary conglomerates and limestones. A geotechnical testing program was carried out on undisturbed samples from Sultan Qaboos University staff housing areas where building damage had occurred, to evaluate mineralogical composition, cation content and swelling characteristics. The test results characterized these soils/rocks as highly expansive type with Na-smectite as the dominant clay mineral. 相似文献
7.
M. Cathelineau 《Mineralium Deposita》1983,18(1):89-97
A comprehensive study of alteration minerals, especially clays, developed around or within French hydrothermal uranium ore bodies (Vendée and Margeride), generally associated with leucogranitic rocks, using optical examinations, classical methods of clay mineralogy and electron microprobe determinations, demonstrates the general feature of potassic minerals as products of reaction between ore forming fluids and host rocks. Six stages of alteration follow the typical metallogenic sequence established for numerous deposits: early stages and uranium stages 1) 2) 3) with phengites, illite, mixed layered illite and K-montmorillonites; 4), early reworking of pitchblende 1 to pitchblende 2 with complex zoning around ores: illite, illite-K-montmorillonites; 5) then to coffinite-smectites; 6) sooty pitchblende, during supergene weathering, with smectites and kaolinite. Potassic metasomatism by fluids in desequillibrium with the minerals of the granitic host rocks, essentially albite, explains the complex alterations in K-smectites, mixed layered minerals and adularia. Variety of alteration products in each alteration zone indicate incomplete reactions of the solids and chemical potential gradients on a small scale. 相似文献
8.
Poikiloblastic index minerals in pelitic rocks from the Orrs Island–Harpswell Neck area of coastal Maine contain inclusion textures that indicate sequential growth of progressively higher grade metamorphic minerals during development of a near-vertical crenulation foliation. The sequence of zones in the field is garnet, staurolite, staurolite–andalusite, staurolite–sillimanite and sillimanite. Inclusion fabrics characteristic of different stages in crenulation cleavage development indicate that index minerals nucleated and grew sequentially: biotite began to grow before deformation, garnet began to grow during early stages of crenulation cleavage development, staurolite grew during intermediate stages, and andalusite grew relatively late, when transposition of the foliation was nearly complete. Muscovite pseudomorphs and sillimanite were mainly post-kinematic. The fact that metamorphic index minerals grew sequentially in individual rocks in the same order in which they appear across the field area indicates that the high temperature part of the pressure–temperature path was similar to the metamorphic field gradient. Metamorphism in the Orrs Island–Harpswell Neck area is consistent with the magmatic heating model that has been proposed for western Maine. Sequential development of index minerals in pelitic rocks in the Orrs Island–Harpswell Neck area apparently resulted from sequential nucleation after substantial overstepping of mineral-forming reactions. Once nucleation of an index mineral had taken place, initial growth was rapid and poikiloblasts preserved inclusion trails characteristic of the prevailing stage of crenulation cleavage development. Because nucleation of sillimanite may have required more overstepping of the andalusite–sillimanite reaction than nucleation at dehydration reactions, determination of metamorphic conditions for rapidly heated rocks such as these by comparison with a petrogenetic grid is problematic. Garnet zoning patterns in these rocks should reflect the fact that growth of garnet interiors occurred early during metamorphism in equilibrium with a low-grade assemblage. Only garnet rims would be expected to record the subsequent pressure–temperature path. 相似文献
9.
The aureoles of the Donegal granites frequently contain combinationsof the following minerals: kyanite, andalusite, fibrolite, sillimanite.Textural and spatial evidence suggests these minerals did notgrow simultaneously but sequentially in the order above, asthe temperature increased in the aureoles. Reactions are notcomplete and overstepping is common. Early porphyroblast phasesdo not take part in later reactions, they remain closed systems.Later reactions take place essentially from the groundmass layeredminerals. Polymorphic change from one aluminium silicate toanother is rare. The presence of more than one polymorph ina rock is therefore due to the metastable persistence of thelower temperature phase(s) which grew stably. Kyanite is confined to rocks with values of MgO/(MgO/FeO) (molecularratios) greater than about 0-50, so that its absence in someaureoles is due to a lack of rocks of the appropriate compositionrather than inadequate pressure during crystallization. Sillimanite,fibrolite, and andalusite show no restriction to rocks of agiven composition. The aureoles in Donegal were probably formedover a relatively narrow pressure band and a wide temperaturerange. 相似文献
10.
11.
Petrology of ultrahigh-pressure eclogites from the ZK703 drillhole in the Donghai, eastern China 总被引：25，自引：0，他引：25
The 558-m-deep ZK703 drillhole located near Donghai in the southern part of the Sulu ultrahigh-pressure metamorphic belt, eastern China, penetrates alternating layers of eclogites, gneisses, jadeite quartzites, garnet peridotites, phengite–quartz schists, and kyanite quartzites. The preservation of ultrahigh-pressure metamorphic minerals and their relics, together with the contact relationship and protolith types of the various rocks indicates that these are metamorphic supracrustal rocks and mafic-ultramafic rock assemblages that have experienced in-situ ultrahigh-pressure metamorphism. The eclogites can be divided into five types based on accessory minerals: rutile eclogite, phengite eclogite, kyanite–phengite eclogite, quartz eclogite, and common eclogite with rare minor minerals. Rutile eclogite forms a thick layer in the drillhole that contains sufficient rutile for potential mining. Two retrograde assemblages are observed in the eclogites: the first stage is characterized by the formation of sodic plagioclase+amphibole symplectite or symplectitic coronas after omphacite and garnet, plagioclase+biotite after garnet or phengite, and plagioclase coronas after kyanite; the second stage involved total replacement of omphacite and garnet by amphibole+albite+epidote+quartz. Peak metamorphic P–T conditions of the eclogites were around 32 to 40 kbar and 720°C to 880°C. The retrograde P–T path of the eclogites is characterized by rapidly decreasing pressure with slightly decreasing temperature. Micro-textures and compositional variations in symplectitic minerals suggest that the decompression breakdown of ultrahigh-pressure minerals is a domainal equilibrium reaction or disequilibrium reaction. The composition of the original minerals and the diffusion rate of elements involved in these reactions controlled the symplectitic mineral compositions. 相似文献
12.
David Savage Josep M. SolerKohei Yamaguchi Colin WalkerAkira Honda Manabu InagakiClaire Watson James WilsonSteven Benbow Irina GausJoerg Rueedi 《Applied Geochemistry》2011,26(7):1138-1152
The use of cement and concrete as fracture grouting or as tunnel seals in a geological disposal facility for radioactive wastes creates potential issues concerning chemical reactivity. From a long-term safety perspective, it is desirable to be able model these interactions and changes quantitatively. The ‘Long-term Cement Studies’ (LCS) project was formulated with an emphasis on in situ field experiments with more realistic boundary conditions and longer time scales compared with former experiments. As part of the project programme, a modelling inter-comparison has been conducted, involving the modelling of two experiments describing cement hydration on one hand and cement-rock reaction on the other, with teams representing the NDA (UK), Posiva (Finland), and JAEA (Japan).This modelling exercise showed that the dominant reaction pathways in the two experiments are fairly well understood and are consistent between the different modelling teams, although significant differences existed amongst the precise parameterisation (e.g. reactive surface areas, dependences of rate upon pH, types of secondary minerals), and in some instances, processes (e.g. partition of alkali elements between solids and liquid during cement hydration; kinetic models of cement hydration). It was not conclusive if certain processes such as surface complexation (preferred by some modellers, but not by others) played a role in the cement-rock experiment or not. These processes appear to be more relevant at early times in the experiment and the evolution at longer timescales was not affected. The observed permeability profile with time could not be matched. The fact that no secondary minerals could be observed and that the precipitated mass calculated during the simulations is minor might suggest that the permeability reduction does not have a chemical origin, although a small amount of precipitates at pore throats could have a large impact on permeability.The modelling exercises showed that there is an interest in keeping the numerical models as simple as possible and trying to obtain a reasonable fit with a minimum of processes, minerals and parameters. However, up-scaling processes and model parameterisation to the timescales appropriate to repository safety assessment are of considerable concern. Future modelling exercises of this type should focus on a suitable natural or industrial analogue that might aid assessing mineral-fluid reactions at these longer timescales. 相似文献
13.
Amer A. Al-Rawas 《Engineering Geology》1999,53(3-4):327-350
The factors controlling the expansive nature of the soils and rocks in Northern Oman were studied. Basic geotechnical data from over 40 sites were collected and using empirical relationships, swelling potentials were identified. A laboratory testing program was carried out using undisturbed samples from these swell pressures up to 3.5 MPa, and swell percent values up to 30 were measured. The clay minerals and cations of these samples were determined and Na-smectite was identified as being the main clay-mineral present. Microfabric studies showed generally dense clay matrices. However, these swelling materials exist as impersistent bands with non-swelling soils and rocks which makes prediction of the ground heave problematic. 相似文献
14.
In low- and middle-grade pelitic metamorphic rocks, the extentsof Tschermak substitution in muscovite, chlorite and biotitechange regularly with bulk-rock composition and external conditions.This paper gives a theoretical analysis of the changes. From equipotential lines for Al2O3 plotted on AFM diagrams,we have derived a series of Thompson-type muscovite compositiondiagrams, which show how the celadonite content of muscovitevaries with the associated ferromagnesian minerals or with thebulk-rock composition under constant external conditions. Thedistribution coefficient of the exchange reaction for Tschermaksubstitution between muscovite and chlorite varies greatly notonly with temperature but also with the extent of this substitutionin the two minerals because of their strong deviation from ideality.Muscovites with a high celadonite content (phengites) occurin low-temperature rocks in any of the high-, medium- and low-pressuretypes of metamorphism, probably because the exchange equilibriumfor Tschermak substitution between muscovite and chlorite isnot sensitive to pressure. When both Mg-Fe and Tschermak substitutionoccur in muscovite and some other silicates, a metapelite containingthree AFM phases together with muscovite and quartz has at leasttwo independent net-transfer reactions that take place sideby side with changing external conditions. The mass balancerequirement in the rock is imposed on a linear combination ofthe two reaction equations, leading to a constraint on the stoichiometricequations among phase components and the progressive compositionalchanges of muscovite, chlorite and biotite. From such a viewpoint,we examine reactions and progressive mineralogical changes inmetapelites, beginning with K-feldspar-bearing low-grade metapeliticrocks, in which biotite appears by reaction of K-feldspar withchlorite at a temperature lower than that of the biotite isograddefined for K-feldspar-free pelitic rocks. When both Mg-Fe and Tschermak substitution occur in muscoviteand some other silicates, a metapelite containing three AFMphases together with muscovite and quartz has at least two independentnet-transfer reactions that take place side by side with changingexternal conditions. The mass balance requirement in the rockis imposed on a linear combination of the two reaction equations,leading to a constraint on the stoichiometric equations amongphase components and the progressive compositional changes ofmuscovite, chlorite and biotite. From such a viewpoint, we examinereactions and progressive mineralogical changes in metapelites,beginning with K-feldspar-bearing low-grade metapelitic rocks,in which biotite appears by reaction of K-feldspar with chloriteat a temperature lower than that of the biotite isoerad definedfor K-feldsoar-free oelitic rocks. The equations for the reactions that produce biotite or biotite? garnet in K-feldspar-free metapelites have been derived. Combinedwith the composition relations of coexisting muscovite, chlorite,biotite and garnet, they lead to the inference that progressof these reactions with rising temperature causes a decreaseof the celadonite content of muscovite, the antigorite contentof chlorite and the phlogopite content of biotite in the metapelitesof the chlorite, biotite and lower garnet zones, and that thistrend may not continue into the staurolite zone. This inferencehas been verified by examination of the analytical data of mineralsin four progressive metamorphic terranes covering the high-,medium- and low-pressure types. The composition of chlorite is buffered by the garnet-producingreaction so that chlorites in garnet-bearing metamorphic rocksdevelop (Mg ? Fe)/Al2 ratios close to that of almandine at elevatedtemperatures. The maximum possible celadonite content in muscoviteunder given external conditions is realized in K-feldspar-bearingrocks, and decreases with rising temperature. 相似文献
15.
C. Page Chamberlain John M. Ferry Douglas Rumble III 《Contributions to Mineralogy and Petrology》1990,105(3):322-336
To interpret correctly the isotopic composition of metmorphic rocks and minerals, the effect of nettransfer reactions must be quantitatively evaluated. Such evaluation requires a complete set of linearly independent, net-transfer reactions that fully describe the reacting system. The set of net-transfer reactions is then coupled with mass-balance equations for stable isotopes. Reaction spaces can be contoured with isopleths of °18O, °13C, and D of minerals which allows evaluation of the effect of different reactions and bulk compositions on the stable isotopic composition of minerals and rocks. Using this approach, we examined the effect of fractionation of isotopes due to net-transfer reactions at the biotite and second-sillimanite isograds in northern New England. Our analysis shows that the shift in °13C and °18O at an isograd depends strongly upon the overall net-transfer reaction at the isograd and the bulk composition of the rock. The use of model isograd reactions to determine isotopic shifts, therefore, can lead to serious errors in the interpretation of isotopic data. At the second-sillimanite isograd °18O
qtz
(quartz), °18O
kspar
(K feldsdpar), and °18O
wr
(whole rock) decrease by 0.5, 1.0, and 0.8 per mil, respectively. Quantitative evaluation of the effect of fractionation of isotopes by net-transfer reactions shows that: (1) the relative changes in oxygen isotopes across the isograd could be caused by distillation of fluids during develatilization reactions; (2) the magnitude of the observed isotopic shifts often differs by a factor of 2 from the calculated shifts due to reaction progress alone. The difference between observed and calculated shifts is attributed to either, differences in bulk composition between individual rocks, or, to isotopic exchange between minerals after peak metamorphism. At the biotite isograd the shifts in carbon and oxygen isotope values are different from predicted shifts caused by net-transfer reactions alone. This discrepancy suggests that fluids infiltrated the rocks during the formation of the biotite isograd. 相似文献
16.
大别山区变质岩中蓝晶石的几种退变质反应及其所指示的动力学过程 总被引：3，自引：2，他引：3
蓝晶石在大别山含柯石英和不含柯石英的榴辉岩、高压变质的副片麻岩、非高压变质的宿松群的变质沉积岩中都是重要的变质矿物。它们多有冠状或其它的变质反应结构，形成多样化的退变质反应矿物。有些退变质反应是十分罕见的。本文报道了８种蓝晶石的矿物组合和退变质反应，推测和计算了变质反应的温度－压力条件，从而探讨了它们代表的近等温降压、升温降压和流体为重要因素的降温降压的不同的动力学过程。这些数据与用其它变质矿物所得到的温度压力条件和ＰＴｔ演化基本一致。为探讨大别山超高压变质带的构造演化提供了新的依据。 相似文献
17.
《Applied Geochemistry》2002,17(3):207-223
Many designs for geological disposal facilities for radioactive and toxic wastes envisage the use of cement together with bentonite clay as engineered barriers. However, there are concerns that the mineralogical composition of the bentonite will not be stable under the hyperalkaline pore fluid conditions (pH > 12) typical of cement and its properties will degrade over long time periods. The possible extent of reaction between bentonite and cement pore fluids was simulated using the reaction-transport model, PRECIP. Key minerals in the bentonite (Na-montmorillonite, analcite, chalcedony, quartz, calcite) were allowed to dissolve and precipitate using kinetic (time-dependent) reaction mechanisms. Simulations were carried out with different model variants investigating the effects of: temperature (25 and 70 °C); cement pore fluid composition; dissolution mechanism of montmorillonite; rates of growth of product minerals; solubilities of product minerals; and aqueous speciation of Si at high pH. Simulations were run for a maximum of 3.2 ka. The results of all simulations showed complex fronts of mineral dissolution and growth, driven by the relative rates of these processes for different minerals. Calcium silicate hydrate (CSH) minerals formed closest to the cement-bentonite boundary, whereas zeolites and sheet silicates formed further away. Some growth of primary bentonite minerals (analcite, chalcedony, calcite and montmorillonite) was observed under certain conditions. Most alteration was associated with the fluid of highest pH, which showed total removal of primary bentonite minerals up to 60 cm from the contact with cement after ∼1 ka. The maximum porosity increase observed was up to 80–90% over a narrow zone 1–2 cm wide, close to the cement pore fluid- bentonite contact. All simulations (except that with alternative aqueous speciation data for Si) showed total filling of porosity a few cms beyond this interface with the cement, which occurred after a maximum of 3.2 ka. Porosity occlusion was principally a function of the growth of CSH minerals such as tobermorite. There was very little difference in the alteration attained using different model variants, suggesting that bentonite alteration was not sensitive to the changes in parameters under the conditions studied, so that transport of pore fluid through the bentonite governed the amount of alteration predicted. Principal remaining uncertainties associated with the modelling relate to assumptions concerning the evolution of surface areas of minerals with time, and the synergy between changing porosity and fluid flow/diffusion. 相似文献
18.
试论阜平杂岩的深熔作用 总被引：2，自引：0，他引：2
阜平杂岩中广泛产出浅色脉体,从而显示强烈的混合岩化作用。前人把引起混合岩化作用的机制归因于岩汁交代、重熔或无水深熔作用,似乎与实际的岩相结构不是很一致。矿物自形晶、钠长石净边结构和一些典型的矿物转化反应表明,阜平杂岩的混合岩化作用实际上经历了复杂的过程,主要表现为有水条件下的深熔作用。所形成的熔体有较大的流动性,可迁移一定的距离而进入邻近的岩石,对这些部位而言相当于发生了外来熔体的注入活动,造成熔体注入式混合岩化作用,形成一些交代反应和结构。因此,阜平杂岩混合岩化作用中的变质反应过程既包括长英质矿物的熔融(溶解),还涉及一种含水矿物(如黑云母)转化形成另外一种含水矿物(如角闪石)的化学反应。阜平杂岩的混合岩化作用最重要的机制是水致熔融或含水深熔作用,溶解性重熔或无水深熔作用则较为次要。 相似文献
19.
R. L. GIBSON 《Journal of Metamorphic Geology》1992,10(5):637-650
The sequence of growth of garnet, staurolite and aluminosilicate in Fe-rich metapelitic rocks from the Canigou massif, Pyrenees, is established using evidence of inclusion, reaction and pseudomorphing textures between the different minerals, compositional zoning patterns in garnet and staurolite (that can be related to the KFMASH reaction grid), and the geometric relations between inclusion trails in the porphyroblasts and the matrix microstructures. The evidence indicates that garnet and staurolite commenced growth before aluminosilicate in all cases, even where all three are in textural equilibrium. Interpretation of the reaction textures between the porphyroblasts and of the compositional zoning in garnet and staurolite in terms of the KFMASH reaction grid indicates the importance of continuous reactions in the development of these phases. Some garnet and staurolite porphyroblasts underwent renewed growth during breakdown, producing rims enriched in Mn and Zn respectively. The presence of aluminosilicate in these assemblages (i.e. the absence of a clear andalusite-absent zone in the field) is attributed to a strong pressure-dependence for the aluminosilicate-producing reactions. Porphyroblast-matrix microstructural relations indicate that Hercynian metamorphism in the massif was synchronous with the development of the regional subhorizontal foliation (S3). 相似文献
20.
华南海岸沙丘岩的特征及其形成发育模式 总被引：10，自引：0，他引：10
海岸沙丘岩是一种热带、亚热带干旱及季节性湿润地区特有的碳酸盐胶结的风成碎屑岩。本文对华南沿海沙丘岩的沉积结构、沉积构造特征,地球化学与古生物特征,及其胶结类型、成岩机制和发育模式进行了较系统研究,并讨论了与海滩岩的区别。 相似文献