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1.
文章综合分析研究了中国21个夕卡岩矿床中的130个角闪石的成分分析数据。根据夕卡岩类型及其伴生金属矿化的不同，把角闪石分为4大类：钙夕卡岩中的角闪石多属钙角闪石，包括绿钙闪石、铁角闪石、镁绿钙闪石、铁浅闪石、阳起石、铁阳起石、铁镁钙闪石和铁韭闪石等；镁夕卡岩中的角闪石以透闪石为主，局部有浅闪石或韭闪石；锰质夕卡岩中的角闪石有锰质阳起石、锰质透闪石、锰直闪石和锰镁闪石；碱质夕卡岩中的角闪石属钠-钙角闪石或钠角闪石类，包括钠透闪石、镁亚铁钠闪石、亚铁钠闪石、镁铝钠闪石和镁钠闪石。碳酸盐围岩和有关侵入岩的成分对角闪石的类型、成分及其伴生金属矿化起重要的作用。 相似文献
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利用增量方法和同位素交换技术,对角闪石族矿物的氧同位素分馏进行了理论计算和实验测定。理论结果表明,不同化学成分的角闪石之间存在一定的氧同位素分馏,其13O富集顺序为:钠闪石>蓝闪石>铁闪石>阳起石=镁铁门石≥直闪石≥透闪石>普通角闪石>铝直闪石>韭闪石。高温条件下(>500℃),角闪石相对于水亏损18O达1‰至3‰。实验进行在有少量流体存在的条件下,温度为520℃至680℃。所确定的方解石-透闪石氧同位素分馏系数与理论计算值在误差范围内完全一致。理论和实验确定的石英-透闪石分馏曲线均显着低于已知的经验校准曲线,反映了变质岩中含角闪石矿物集合体内部的退化同位素再平衡。 相似文献
3.
赣东北高压变质岩的岩石类型、矿物组成与变质过程 总被引：6，自引：1，他引：6
赣东北高压变质岩包括含硬玉霓辉石钠长角闪片岩、含硬玉霓辉石石英钠长石岩、含霓辉石角闪石英钠长石岩、含霓辉石钠长角闪片岩、蓝透闪石石英钠长石岩、镁钠闪石石英钠长石岩等岩石类型，主要组成脏矿物为硬玉、霓辉石、镁钠闪石、蓝透闪石、镁角闪石、阳起石、石英、钠长石、金红石和榍石。研究表明，高压变质峰期后经历了近等温降压退变质过程。 相似文献
4.
含紫硅碱钙石、镁钠钙闪石（钠透闪石－石棉）及蓝色办透闪石的碱性交代岩的形成首先是由硅酸和碱（Ｎａ２Ｏ和Ｋ２Ｏ的不同作用）的惰性及ＦｅＯ,ＭｇＯ,ＣａＯ和Ａｌ２Ｏ３的强烈活性决定的,含蓝色软透闪石和镁的钙闪石（钠透闪石－石棉）的交换岩是岩浆期后溶解演化的中期产物,而含紫硅碱钙石的交换岩却是其晚期的产物。 相似文献
5.
勐库地区新近发现的退变质榴辉岩中晚期退变质作用形成的闪石类矿物十分丰富,其携带了大量晚期退变质过程中的岩石成因信息。本文通过系统的矿物学研究,鉴定出了3期10种闪石类矿物,其中以镁钙闪石、镁角闪石、铁镁钙闪石、铁韭闪石、透闪石、阳起石等钙质闪石类为主,有少量冻蓝闪石、蓝透闪石等钠-钙闪石类。研究发现,随着退变质过程中时间的推移,角闪石的形成环境逐渐由还原环境向弱氧化环境、氧化环境演变。根据角闪石电子探针成分测试结果计算了相应的温度、压力条件。结合岩相学的资料,将退变质过程分为3期:(1)第1期早阶段为近等温降压过程(p=0.56~0.75 GPa,t=642~709℃),主要形成铁韭闪石、铁镁钙闪石、镁钙闪石;晚阶段为等温降压过程(p=0.39~0.56 GPa,t=619~642℃),主要形成镁钙闪石及少量镁绿钙闪石、铁韭闪石;(2)第2期为降温降压过程(p=0.23~0.42 GPa,t=460~610℃),主要形成镁角闪石、冻蓝闪石及铁角闪石;(3)第3期为近等温降压过程(p=0.09~0.31 GPa,t=350~420℃),主要形成透闪石、阳起石、蓝透闪石等。闪石类的成分变化反映了退变质榴辉岩从地壳底部的角闪石榴辉岩-高压麻粒岩相温压环境向中上地壳角闪岩相、绿片岩相温压环境的渐次退变质作用过程。这与昌宁-孟连构造带上印支期的碰撞造山作用、燕山期的区域性地壳伸展、喜马拉雅期的陆内造山运动具有较好的对应关系。 相似文献
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75年北大黄福生等同志在该铁矿工作时,已发现在磁铁石英岩中有两种碱性闪石,由于它们产在富铁矿体中及其附近,因而引起了在该区工作的各单位同志的注意。为了研究它们和富铁矿成因关系及对其确切定名,我们对其中一种碱性闪石进行了较详细的研究,确定为钠——钙角闪石族的高铁——蓝透闪石。 相似文献
9.
在中国中部晚太古代五河群的碱性片麻岩中,曾报导有蓝色角闪石和硬玉的存在,并且认为它们是与安徽张八岭群同期的高压变质矿物。本文作者经过对岩石和矿物成分的详细研究,证实五河群中的碱性角闪石+锥辉石+斜长石+黑云母+石英±钠长石±赤铁矿等矿物组合是典型的角闪岩相变质矿物组合,这些碱性角闪石的核部是岩浆岩成因的镁钠铁闪石,其边部是角闪岩相变质成因的镁钠闪石,这些碱性闪石的Al_2O_3含量特别低,而FeO和Fe_2O_3含量很高,它们与张八岭群的青铝闪石在化学成分上差别很大。五河群片麻岩中的钠质辉石是很纯的锥辉石而没有硬玉组分。从含大量微斜长石的矿物组合、蓝色角闪石的矿物成分、低硬玉质的钠辉石和估算的温度和压力条件来看,我们认为五河群的片麻岩并不是高压蓝闪片岩相的变质产物。此外,以前关于五河群和中国中部其他变质岩中(如张八岭群)有关硬玉的报导中所发表的电子探针和化学分析资料与辉石的化学分子式不符,我们的岩石学研究也没有证实硬玉的存在。 相似文献
10.
缅甸是世界上优质翡翠的最重要产地,角闪石族矿物是缅甸翡翠中的常见矿物。对缅甸翡翠原石进行手标本、薄片偏光显微镜观察和电子探针测试,结果表明,翡翠原石组成矿物的形成顺序为岩浆锆石→热液锆石和硬玉→绿辉石→Ca质角闪石→Na-Ca、Na质角闪石→钠长石,岩石形成后受到后期应力作用使部分角闪石族矿物发生变形。Ca质角闪石形成后,晚期Na-Al-Si流体和富Ca、Mg和Fe的浅闪石发生反应,形成了Na-Ca质、Na质角闪石,包括钠透闪石,蓝闪石和镁铝钠闪石。随压力的降低,残余流体在早期形成矿物颗粒之间沉淀结晶出钠长石。矿物的化学成分和矿物种类及结构对翡翠的品质有重要影响,硬玉中的Cr及角闪石矿物的存在导致了翡翠绿色深浅的变化。组成矿物的形态及颗粒大小、排列的紧密程度,影响翡翠的质地和透明度等外观特征。 相似文献
11.
N. G. Konopleva G. Yu. Ivanyuk Ya. A. Pakhomovsky V. N. Yakovenchuk Yu. P. Men’shikov Yu. A. Korchak 《Geology of Ore Deposits》2008,50(8):720-731
The rocks of the Khibiny pluton contain 25 amphibole varieties, including edenite, fluoredenite, kaersutite, pargasite, ferropargasite, hastingsite, magnesiohastingsite, katophorite, ferrikatophorite, magnesiokatophorite, magnesioferrikatophorite, magnesioferrifluorkatophorite, ferrimagnesiotaramite, ferrorichterite, potassium ferrorichterite, richterite, potassium richterite, potassium fluorrichterite, arfvedsonite, potassium arfvedsonite, magnesioarfvedsonite, magnesioriebeckite, ferriferronyboite, ferrinyboite, and ferroeckermannite. The composition of rock-forming amphiboles changes symmetrically relative to the Central Ring of the pluton; i.e., amphiboles enriched in K, Ca, Mg, and Si are typical of foyaite near and within the Central Ring. The Fe and Mn contents in amphiboles increase in the direction from marginal part of the pluton to its center. Foyaite of the marginal zone contains ferroeckermannite, richterite, arfvedsonite, and ferrorichterite; edenite is typical of foyaite and hornfels of the Minor Arc. Between the Minor Arc and the Central Ring, foyaite contains ferroeckermannite, arfvedsonite, and richterite; amphiboles in rischorrite, foidolite and hornfels of the Central Ring are (potassium) arfvedsonite, (potassium) richterite, magnesiokatophorite, magnesioarfvedsonite, ferroeckermannite, and ferriferronyboite; amphiboles in foyaite within the Central Ring, in the central part of the pluton, are arfvedsonite, magnesioarfvedsonite, ferriferronyboite, katophorite, and richterite. It is suggested that such zoning formed due to the alteration of foyaite by a foidolite melt intruded into the Main (Central) Ring Fault. 相似文献
12.
Diana S. Sutherland 《Contributions to Mineralogy and Petrology》1969,24(2):114-135
During alkali metasomatism of the country-rock associated with ijolite-carbonatite complexes the development of sodic amphibole and/or pyroxene is characteristic. In this paper, some new chemical analyses of these minerals, together with published analyses from fenites of Kenya, Uganda and Tanzania, include those of co-existing pairs of amphibole and pyroxene. The common amphiboles of the fenites are magnesioarfvedsonites with 100 Mg: Mg+Fe+Mn ranging from 67 to 36. They co-exist with aegirines having 0.75 to 0.89 ions Fe+3. Most of these minerals are poor in Ca; co-existing pairs tend to show corresponding increases in Ca and in Fe+2. In the syenitic fenites of Tororo and Budeda, considered to have formed at higher temperatures, the stable mineral is aegirine-augite. New analyses of richterite, magnesioarfvedsonite and aegirine from carbonate-rich rocks are also presented, and the relation between fenites and carbonatites is discussed. 相似文献
13.
The composition and structure of synthetic (Na,K)-richterites have been characterized by EMP, HRTEM, XRD and FTIR methods. Despite the fact that the syntheses were done on bulk compositions along the richterite-K-richterite binary, EMP analyses and FTIR spectra indicate that the amphiboles are not simple solid solutions of the two richterite endmembers richterite and K-richterite alone, but tremolite and Mg-cummingtonite components are also present in considerable amounts. HRTEM observations show that the amphiboles are structurally well ordered. Only a very few chain multiplicity faults are present. XRD examination reveals lattice parameters of 9.9055 Å, 17.9844 Å, 5.2689 Å and 104.212° for richterite and 10.0787 Å, 17.9877 Å, 5.2715 Å and 104.878° for K-richterite endmembers. The unit cell volumes are 909.90 Å3 and 923.61 Å3 for richterite and K-richterite, respectively. The lattice parameters a and β for K-richterite are considerably larger than those published previously implying that those were not determined for pure K-richterite. The positions of the characteristic OH-stretching vibrations in the IR for sodium-potassium (3729.8–3734.8 cm?1) and vacancies (3671.1–3675.4 cm?1) on the A-site are in agreement with earlier determinations. Using synthetic tremolite as a standard the vacancy concentration on the A-site of the synthetic (Na,K)-richterites was determined quantitatively by FTIR-spectroscopy. The OH-stretching vibration of this synthetic tremolite is at 3674.5 cm?1. It is assigned to a local coordination with 3 Mg (2 M1+M3) as nearest neighbors and with 2 Ca (M4) as next nearest neighbors. A well resolved band with a smaller intensity is located at 3669.2 cm?1, which is attributed to a configuration including Ca+Mg on M4 instead of only Ca. 相似文献
14.
贵州白坟钾镁煌斑岩中钾碱镁闪石的研究 总被引：1，自引：0，他引：1
本文简要总结了近年有关钾镁煌斑岩的定义、矿物学及其地球化学研究的成果；讨论了钾碱镁闪石在钾镁煌斑岩研究中的意义；回顾了钾碱镁闪石的词源及其分类定名方法，详细介绍了贵州镇远地区白坟岩带中钾碱镁闪石的矿物学特征及其成分特征。 相似文献
15.
Rolf Zimmermann M. Gottschalk Wilhelm Heinrich Gerhard Franz 《Contributions to Mineralogy and Petrology》1997,126(3):252-264
The cation exchange equilibrium has been investigated by hydrothermal experiments at 700 and 800°C at 200 MPa. To avoid equilibration problems of conventional exchange experiments, we synthesized amphiboles with an excess fluid allowing exchange between solid and fluid during the experiment. The exchangeable cations Na and K were provided as excess 1 to 2n chloridic solution. These exchange syntheses can be described by the reaction equation with (aq) for hydroxides and chlorides in aqueous solutions and ( s ) and ( p )?=?start and product fluid. The amphiboles grew in presence of the exchange fluid and adjusted their stoichiometry in equilibrium with the fluid phase. The solid products consist of more than 99% amphibole (Na,K-richteritess) with traces of diopside and quartz. The amphiboles are up to 1?mm long and often ≈ 40 μm thick. Detailed EMP- and HRTEM-observations show that they are chemically homogeneous and structurally wellordered. The experimental results give consistent phase relations in the reciprocal ternary system Na-richterite–K-richterite–NaCl–KCl. We analysed the product fluid with AAS- and ICP-methods. The Na-K distribution coefficients between fluid and amphiboles of the richterite–K-richterite join are close to unity at 700°C and 800°C at 200 MPa. Small systematic deviations are explained by a symmetric solution model for the A-position of the amphiboles. Using ideal mixing for H2O-NaCl-KCl fluids, a mixing model for the system richterite–K-richterite is presented. We suggest that the composition of richterite solid solutions can be used as a sensor for NaCl/KCl-ratios in metamorphic fluids. 相似文献
16.
Manganese silicate rocks, interbanded with manganese oxide orebodies, constitute an important stratigraphic horizon in the Mansar formation of the Sausar Group of Precambrian age in India. The manganese silicate rocks of Gowari Wadhona occupy the westernmost flank of the manganese belt of the Sausar Group. These rocks are constituted of spessartite, calcium-rich rhodonite, quartz, manganoan diopside, blanfordite (manganese bearing member of diopside-acmite series), brown manganese pyroxene (manganese bearing aegirine-augite), winchite (manganese bearing richterite-tremolite), juddite (manganese bearing amphibole with richterite, tremolite, magnesioriebeckite and glaucophane molecules), tirodite (manganese bearing amphibole with richterite, cummingtonite and glaucophane molecules), manganophyllite, alurgite, piedmontite, braunite, hollandite (and other lower oxides of manganese) with minor apatite, plagioclase, calcite, dolomite and microcline. A complete mineralogical account of the manganese-bearing phases has been given in the text. It has been shown that the juxtaposition of manganese silicate rocks with dolomitic marble, regional metamorphism to almandine-amphibolite facies and assimilation of pegmatite veins cutting across the manganese formation, were responsible for the development of these manganese silicate rocks and the unusual chemical composition of some of the constituent minerals. It has been concluded that the manganese silicate rocks of Gowari Wadhona were originally laid down as sediments comprising manganese oxides admixed with clay, silica etc. and were later regionally metamorphosed to almandine-amphibolite facies. All evidences indicate that rhodochrosite was not present in the original sediment and the bulk composition of the sediments was rich in manganese. These rocks agree entirely to the detailed nomenclature of the gondites enunciated by Fermor (1909) and amplified by Roy and Mitra (1964) and Roy (1966). 相似文献
17.
Yoshimasu Kuroda Tetsuro Suzuoki Sadao Matsuo Ken -ichiro Aoki 《Contributions to Mineralogy and Petrology》1975,52(4):315-318
The water content and D/H ratio of pairs of phlogopite and richterite in kimberlite samples were measured. The water contents of both minerals were lower than the formula content. On the basis of D/H ratios of the pair, phlogopite and richterite can not be regarded as a simple equilibrium product with respect to hydrogen isotope exchange. It seems impossible to estimate D/H ratio of the mantle water through D/H ratios of the hydrous silicate pairs. 相似文献
18.
Ken-ichiro Aoki 《Contributions to Mineralogy and Petrology》1975,53(3):145-156
Peridotite xenoliths containing primary phlogopite with or without potassic richterites as major constituent (up to 12 vol. %) are rarely found in kimberlite from the Bultfontein Floors. Chemically, these rocks are similar in compositions with those of the granular type garnet peridotite xenoliths from South Africa and Lesotho, except for an abnormally high content of K2O in the former. Phlogopite and potassic richterite are thought to have the following genesis: garnet peridotites at a depth from 170 to 100 km suffered local introduction of a potash-rich fluid, and garnet and enstatite reacted with this fluid to form phlogopite and diopside. Potassic richterite may have been produced by the reaction between diopside and fluid at the same time as crystallization of phlogopite at depths shallower than 120 km. 相似文献
19.
Drilling-intensive aquifer characterization techniques have been used to obtain depth-discrete water samples from a thick,
hydrogeologically continuous unconfined aquifer system; groundwater results indicate that carbon tetrachloride contamination
is widespread and extends deeper and at concentrations much higher than detected in monitoring networks at the water table.
Carbon tetrachloride, a legacy waste, was used in the plutonium extraction process at the Hanford site in south-central Washington
State. Vertical, depth-discrete groundwater samples were collected during well drilling throughout a 28-km2 region to determine the concentration of carbon tetrachloride present as a dissolved phase in the aquifer. Results indicate
that high concentrations of carbon tetrachloride, three orders of magnitude above the allowable regulatory limit, are present
at depths greater than 25 m beneath the water table. In support of future efforts to remediate the carbon tetrachloride contamination,
it is imperative to locate the remaining chemical inventory, determine the vertical as well as the lateral distribution of
this contaminant and its physical form. Depth-discrete aquifer characterization throughout the uppermost-unconfined aquifer
system is providing this information and improving the understanding of the contaminant distribution and the hydrogeologic
framework through which it moves.
相似文献
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