结晶釉的硅灰石研究

本文导报利用天然矿物岩石为原料配制晶釉釉料的实验，并对形成硅灰石结晶釉的条件及釉析晶的晶体化学、形态学特征进行了讨论。     

用天然矿物配制结晶釉釉料的研究

用天然矿物配制结晶釉釉料的研究李嘉陈代璋杨中漪陈光辉陈彤彤（中国地质大学，北京１０００８３）关键词天然矿物结晶釉陶瓷结晶釉是具有人工晶花的釉体，种类很多，有硅锌矿结晶釉、金红石结晶釉、赤铁矿结晶釉等。这些结晶釉用于装饰陶瓷品，有良好的艺术效果，故亦称...     

中国东部几个地区新生代玄武岩中单斜辉石—熔体平衡温压—兼论幔源包体的成因

以中国东部宽甸、汉诺坝和明溪含有幔源包体的新生代玄武岩中的单斜辉石斑（巨）晶为研究对象,采用最新的单斜辉石－熔体平衡温压计对单斜辉石斑（巨）晶－熔体进行了平衡温压计算。结果表明,碱性玄武岩中的单斜辉石斑晶结晶温度和压力高于共生的亚碱性玄武岩中的单斜辉石斑晶,单斜辉石巨晶的结晶温度和压力高于单斜辉石斑晶。这说明碱性玄武岩的形成深度大于亚碱性玄武岩,单斜辉石巨晶是更高压力下的结晶产物,单斜辉石斑晶在岩浆上升的不同深度均有晶出。回归分析表明,尽管携带幔源包体的玄武岩浆上升速度较快,但并不是绝热上升。单斜辉石斑（巨）晶的结晶温压条件与同一地点幔源包体平衡温压条件的对比表明,单斜辉石巨晶和碱性玄武岩中的部分单斜辉石斑（巨）晶的结晶温压大于幔源包体的平衡温压,表明了包体寄主岩浆的来源深度大于包体的深度。因此,幔源包体是寄主岩浆上升途中捕虏的上地幔碎块,而非寄主岩浆形成源区的残留体。     

大别山绿辉石晶体结构的再研究—兼与谢窦克等同志商榷

谢窦克等曾测定了大别山一个绿辉石的晶体结构，认为它具Ｐ２／ｃ空间群；四面体链分别呈ＳＡ和ＯＢ扭转；Ｍ阳离子日位全部为６次配位的八面体：Ａｌ在所有这四种晶位另均有相当多的占有率，为绿辉石的新型结构。本文对该资料再研究后确认其真实空间群为Ｐ２／ｎ；结构中仅有一种Ｏ旋转的四面体链；Ｍ２和Ｍ２晶位为８次配位；Ａｌ全部进入Ｍ１（１）晶位，Ａｌ－Ｍｇ呈完全有序分布，属典型的Ｐ２／ｎ有序绿辉石。本文给出了重新计     

硬玉及相关辉石化学成份与翡翠玉种研究

1987年国际新矿物和矿物命名委员会表决通过了“辉石的命名”方案。其中Na辉石和Ca-Na辉石的命名仅考虑了硬玉－霓石－Ca-Mg-Fe辉石三元系，并且用Ca-Mg-Fe辉石组份80％和20％的界限划分Ca-M-Fe辉石、绿辉石和硬玉。近17年硬玉和相关辉石的研究已经证实存在硬玉－霓石－Ca-M-Fe辉石－钠铬辉石四元系，只有用50％规则才能对四元系四面体矿物命名。在这个新的命名系统中保留了绿辉石名称，但它仅限于具P2空间群的绿辉石，把C2绿辉石分别归属硬玉和Ca-M-Fe辉石。翡翠玉种和硬玉的化学成份密切相关，据此划分了若干硬玉亚种。使用50％规则命名硬玉，翡翠的传统概念不必作太多的修改。     

绿辉石流变学研究的某些进展

简要概述了绿辉石的晶体结构、反相畴、显微构造及其变形机制等方面的研究现状与进展。结合大别山榴辉岩中的最新研究成果，着重讨论了其构造物理学研究意义，认为绿辉石晶体结构的有序化不仅是温度和化学成分的函数，而且是晶内应变程度的函数。     

英安岩中高压辉石巨晶的发现及其意义

在吉林省九台市官马山晚侏罗世英安岩中发现了辉石巨晶。研究表明。该巨晶不是英安岩浆的结晶产物，英安岩的岩相关及地球化学特征显示，它是酸性流纹岩浆与基性偏碱性的玄武岩浆经混合作用形成的，辉石巨晶是后一种岩浆在高压条件下结晶的产物，对辉石巨晶的温压计算结果表明，该矿物结晶温度为１２７６℃，压力为１．２７ＧＰａ。这一深度可相当于该区软流层的顶界。可以认为，晚侏罗－早白垩世火山岩形成于地壳较厚的环境。     

玻镁安山岩中辉石枝晶的形貌与晶体生长方式

川西乡城地区的玻镁安山岩基质中辉石微晶具有奇特的枝晶形貌。通过高倍率光学显微镜和扫描电镜观察,较详细地分析了辉石枝晶的形貌细节。辉石枝晶一般发育三级分枝,各分枝间以近于90°和110°交角沿单斜辉石结晶学主轴方位优先生长,各级分校具有整体一致的光学性质,如同单个晶体。玻镁安山岩浆流动性大,呈薄层状。快速冷凝作用和强的结晶能力是辉石枝晶发育的前提条件。初步探讨了在远离平衡态结晶时,辉石枝晶生长方式和界面稳定性对晶体形貌的控制作用。     

吉林南部太古宙辉石花岗岩的成因

吉林南部太古宙辉石花岗岩类具有与英云闪长质－奥长花岗岩质－花岗闪长质片麻岩（ＴＴＧ）及深熔钾长花岗岩不同的特征，并不是ＴＴＧ岩系的一部分。地质学、岩石学及地球化学研究表明，该辉石花岗岩类是壳源岩浆结晶分异作用的结果，其岩浆演化主要受早期结晶的辉石、斜长石及角闪石等矿物相的制约。     

危地马拉与缅甸含绿辉石翡翠的矿物学对比研究

以危地马拉蓝水料与缅甸油青种翡翠为研究对象,通过显微镜观察、岩石薄片观察、X射线粉末衍射分析、激光拉曼光谱分析、扫描电镜分析、电子探针分析等测试手段对两者进行了常规宝石学特征、结构特征、杂质矿物、化学成分等方面的对比研究。结果表明,危地马拉蓝水料发育等粒变晶结构,主要成分为硬玉,含有绿辉石,硬玉环带以2～3层为主,绿辉石分别以自形颗粒、交代残余、沿微裂隙充填3种形式存在,其中白色点状物为钠长石,绿色点状物为霓辉石和绿辉石的混杂物;缅甸油青种翡翠以硬玉为主颗粒相对粗大,呈柱粒状镶嵌结构,硬玉发育3～5层环带结构,绿辉石以脉状充填硬玉颗粒间隙或被硬玉颗粒交代呈孤岛状。危地马拉蓝水料硬玉颗粒与脉状绿辉石的CaO含量均高于缅甸油青种翡翠,另外由于霓辉石的存在,推测两产地翡翠结晶环境中的Ca、Fe含量可能存在差异。     

山东大疃榴辉岩和石榴透辉石岩的成因

山东大疃迟家店和石榴二辉橄榄岩中榴辉岩与石榴透辉石岩呈过渡关系，前者位于中心，后者为边缘带，在边缘带的透辉石中出现不规则状和条纹状绿辉石，通过对两类岩石的岩石学，矿物学特征及岩石平衡温压条件的研究，并与国内外不同地区，不同产状同类岩石进行一对比后认为，二者的关系虽然基本符合常见蚀变规律，即中心的榴辉石中绿辉石蚀变成透辉石，从而形成石榴透辉石岩边缘带，但是根据榴辉岩，石榴透辉石岩的ＲＥＥ特征和岩石平     

翡翠的矿物组成特征及其质量

通过翡翠的矿物组成研究 ,其主要由辉石族的矿物 (硬玉、绿辉石、霓石、钠铬辉石 )组成 ,还有少量的闪石族矿物、长石族矿物以及绿泥石和铬铁矿、褐铁矿、赤铁矿等组成 ,他们的含量变化直接影响着翡翠的种类。在矿物组成中 ,硬玉呈不同的绿色 ,这些颜色的多少与分布特征直接影响着翡翠的颜色特征和档次。绿辉石、钠铬辉石含量少 ,在翡翠中呈黑绿色 ,它们的存在使翡翠的档次降低。闪石族矿物主要是蓝色的钠铝质闪石 ,翡翠中的飘“蓝花”就是由于它们造成的。长石族矿物主要是钠长石 ,颗粒细小 ,在翡翠中其含量 1.0 %～ 8.0 %。翡翠中主要的矿物形态以粒状为主 ,矿物的颗粒越细 ,翡翠的透明度、质地也越好。建议将翡翠定义为 :“在地质作用过程中主要由钠质或钠钙质辉石组成的达到玉级的集合体。”     

Chemistry,mineralogy and petrology of an eclogite from the type locality (Saualpe,Austria)

An eclogite and five of its coexisting minerals (omphacite, garnet, carinthine, kyanite and zoisite) from the probable type locality of eclogites (Kupplerbrunn, Saualpe, Austria) described by Haüy (1822) have been analysed. Optical and X-ray data for these minerals are also given. Comparison of the Kupplerbrunn rock with those of other eclogites from the Saualpe region indicates they all have roughly similar compositions. When plotted on an A-C-F diagram the majority of these analyses fall in the region of kyanite-bearing eclogites suggested by Tilley (1936) although the Kupplerbrunn rock is the only sample containing kyanite; the others containing zoisite. The garnet and omphacite compositions of the Kupplerbrunn rock differ markedly from those of other Saualpe eclogites, possibly due to different metamorphic conditions of their formation. Carinthine analyses are all very similar for eclogites from Saualpe. On the basis of geological, analytical and limited experimental evidence, it is postulated that the Kupplerbrunn eclogite was derived from an original gabbroic rock low in water content such that amphibole and zoisite formed from plagioclase, pyroxene and water; omphacite, garnet and kyanite formed from plagioclase and pyroxene, once all the water was used up in the form of amphibole and zoisite. These reactions are believed to have taken place at 5–8 kb pressure at around 600° C; a value close to that suggested by Lodemann (1966) from field data.     

Crystal-chemistry of a unique jadeite-rich acmite-poor omphacite from the Nybø eclogite pod,Sørpollen,Nordfjord, Norway

An omphacite from the Nybø eclogite pod, Norway, has a chemical composition which plots within the gap, often regarded as a miscibility gap, which is evident in all previous compilations of natural jadeite-rich acmite-poor omphacite compositions. Its cation site populations determined by crystal structure refinement accord well with its chemical composition analysed by electron microprobe. Its disordered space group C2/c symmetry extends the known compositional range of C2/c pyroxene. The postulated miscibility gap is regarded as real and wide at low temperatures, but it appears to narrow with increasing temperature or ultimately with increasing acmite proportion. The adjacent primitive symmetry field appears to initially widen with increasing temperature or increasing acmite proportion, at the expense of the diminishing miscibility gap, before finally closing with further increase.     

A ternary solid solution model for omphacite and its application to geothermobarometry of eclogites from the Middle Adula nappe (Central Alps, Switzerland)

A ternary solid solution model for omphacite with the end-members jadeite (NaAlSi₂O₆), diopside (CaMgSi₂O₆) and hedenbergite (CaFeSi₂O₆) was derived from experimental data from the literature. The subregular solution model, fitted by linear programming, is best suited to omphacites with very little aegirine component in common eclogites. Applying this solution model to the calculation of equilibrium phase diagrams of eclogites from the Adula nappe (Central Alps, Switzerland) results in large stability fields for common eclogite assemblages (garnet+omphacite+quartz+H₂O±kyanite). Within this field the compositions of garnet and omphacite show very little variation. A precise determination of the peak-pressure and temperature is not possible. The occurrence of amphibole, overgrowing the peak-pressure assemblage in fresh eclogite, suggests retrograde re-equilibration, still under eclogite facies conditions. The computation of isopleths for garnet and pyroxene end-members allows the estimation of the pressure and temperature conditions of this re-equilibration event (19–21  kbar, c .  700 °C).     

大别山双河超高压榴辉岩中的水: 微区红外光谱分析

大陆深俯冲板块到一定深度后(约90~110km), 几乎没有含水矿物存在, 超高压岩石中名义上无水矿物(NAMs) 成为俯冲板块中水的主要载体, 是示踪超高压变质流体的重要途径.对大别山双河地区超高压榴辉岩中的石榴石和绿辉石进行了详细的微区傅立叶变换红外光谱(MicroFTIR) 分析.FTIR结果显示所有石榴石和绿辉石颗粒都含有结构水, 以OH的形式存在, 其含量范围分别为(30~1860)×10-6和(360~620)×10-6.榴辉岩全岩水含量为(300~750)×10-6, 表明即使是在超高压变质作用的温压条件下, 榴辉岩也可以至少携带数百10-6的水进入深部地球.对石榴石颗粒内部的多点观察发现, 结构水含量的分布出现2种情况: (1) 颗粒内部的均一分布; (2) 核部水含量高而边部低.石榴石颗粒边部的低水含量可能是抬升过程中由于压力降低引起的H扩散所致, 扩散出来的H可能构成了早期退变质流体的重要来源.对于同一样品来说, 结构水含量在绿辉石和石榴石之间的比值为0.5~3.5.      

Partial eclogitisation of gabbroic rocks in a late Precambrian subduction zone (Zambia): prograde metamorphism triggered by fluid infiltration

Gabbros and eclogites occur closely associated in a 200-km-long and up to 40-km-wide area of the Zambezi Belt in central Zambia. This area is interpreted to represent part of a late Precambrian suture zone, with the mafic rocks being relics of subducted oceanic crust. Gradual stages of prograde transformation from gabbro to eclogite are preserved by disequilibrium textures of incomplete reactions. This resulted in kyanite–omphacite-bearing assemblages for eclogites that have Al-poor bulk compositions. Undeformed eclogites typically preserve features of a former gabbroic texture, reflected by replacements of plagioclase and magmatic pyroxene by eclogite facies minerals. Textures of deformed eclogites range from sheared porphyroclastic to porphyroblastic. Relics of magmatic pyroxene are common and complete eclogitisation occurred only in millimetre to centimetre-scale domains in most of the rocks. No evidence for prograde blueschist or amphibolite facies mineral assemblages was found in eclogites. In contrast, the fine grained intergrowth of omphacite, garnet, kyanite and quartz, which replace former plagioclase or was formed in the pressure shadow of magmatic pyroxene relics, indicates that eclogitisation might have affected the gabbroic protoliths directly without any significant intervening metamorphic reactions. Eclogitisation took place under P–T conditions of 630–690 °C and 26–28 kbar, suggesting a large overstepping (>10 kbar) of reaction boundaries. Eclogitisation was initialised and accompanied by a channelised fluid flow resulting in veins with large, subhedral grains of omphacite, kyanite and garnet. The gabbro-to-eclogite transformation was enhanced by a fluid which allowed the necessary material transport for the dissolution–precipitation mechanism that characterises the metamorphic mineral replacements. The process of eclogitisation was limited by reaction kinetics and dissolution–precipitation rates rather than by the metamorphic P–T conditions. Even though ductile deformation occurred and equilibrium phase boundaries were overstepped, the infiltration of fluids was necessary for triggering the gabbro-to-eclogite transformation.Editorial responsibility: J. Hoefs     

Mechanisms of exsolution in sodic pyroxenes

The free energy curves for simple binary solid solutions with limited miscibility or atomic ordering have been combined to predict the phase relations and exsolution mechanisms for a system in which both ordering and exsolution are possible. The nature of the ordering process affects which exsolution mechanisms may be used. If the ordering is second (or higher) order in character then continuous mechanisms predominate and a ‘conditional spinodal’ (Alien and Cahn, 1976) can be described which operates between ordered and disordered end members. For a first order case, the ordered phase can only precipitate a disordered phase by nucleation and growth. Microstructures in omphacites observed by transmission electron microscopy include exsolution lamellae and antiphase domains and the relations between them in selected specimens have been used to interpret the exsolution mechanisms which operated under geological conditions. It appears that most omphacites undergo cation ordering, and then remain homogeneous or exsolve a disordered pyroxene by spinodal decomposition. The predominance of continuous mechanisms has been used to indicate that the C2/c→P2/n transformation may be second (or higher) order in character. A possible phase diagram for jadeite-augite is presented. It is based on the idea that there should be limited miscibility between the disordered end members at low temperatures and that the cation ordering at intermediate compositions (omphacite) is superimposed on a solvus. It is adequate to explain many of the observed microstructures and fits with petrographic evidence of broad two phase fields between impure jadeite and omphacite and between omphacite and sodic augite. The effect of adding acmite is analogous to increasing temperature so that the phase relations for jadeite-acmite-augite can also be predicted.     

Omphacite breakdown reactions and relation to eclogite exhumation rates

Clinopyroxene + plagioclase (±Hbl ± Qtz) symplectites after omphacite are widely cited as evidence for prior eclogite-facies or high-pressure (HP) metamorphism. Precursor omphacite compositions of retrograde eclogites, used for reconstructing retrograde P–T paths, are commonly estimated by reintegrating symplectite phases with the assumption that the symplectite-forming reactions were isochemical. Comparisons of broadbeam symplectite compositions to adjacent unreacted pyroxene from various symplectites after clinopyroxene from the Appalachian Blue Ridge (ABR) and Western Gneiss Region (WGR) suggest that the symplectite forming reactions are largely isochemical. Endmember calculations based on reintegrated symplectite compositions from the ABR and WGR suggest that a minor Ca-Eskola (CaEs) component (X_CaEs = 0.04–0.15) was present in precursor HP clinopyroxene. WGR symplectites consist of fine-grained (∼1 μm-scale), vermicular intergrowths of Pl + Cpx II ± Hbl that occur at grain boundaries or internally. ABR symplectites contain coarser (∼10 μm-scale) planar lamellae and rods of Pl + Cpx II + Qtz + Hbl within clinopyroxene cores. The contrasting textures correlate with decompression and cooling rate, and degree of overstepping of the retrograde reaction (lamellar: slow, erosionally controlled exhumation with slow/low overstepping; fine-grained, grainboundary symplectite: rapid, tectonic exhumation with rapid/high overstepping). Variations in X_CaEs, X_jd, and X_CaTs of precursor HP omphacite are related to the symplectic mineral assemblages that result from decompression. Quartz-normative symplectities indicate quartz-producing retrograde reactions (e.g., breakdown of precursor CaEs); quartz-free symplectities (e.g., diopside + plagioclase after omphacite) indicate quartz-consuming reactions (jd, CaTs breakdown) outpaced quartz-producing reactions. Electronic supplementary material The online version of this article (doi:) contains supplementary material, which is available to authorized users.     

Statistical mechanical modeling of the kinetics of order-disorder in omphacitic pyroxenes

A kinetic statistical model based upon a one-dimensional Ising lattice reflecting the nature of the pyroxene octahedral strip, and with nearest-neighbor and mean-field interactions, is applied to the order-disorder transformation in omphacitic pyroxenes. The equilibration temperature of a naturally ordered omphacite and the annealing data of Carpenter (1981a) on omphacites from the same sample, when applied to the model, provide time- temperature-transformation relations for both long-range and short-range ordering. Results indicate that cooling times on the order of tens of millions of years are necessary for the development of significant degrees of long-range order under optimum conditions, whereas short-range order is developed on much shorter time scales. These results are in agreement with observations of naturally ordered and disordered omphacites with the exception of omphacites ordered in a low-temperature subduction-zone regime; the results support the hypothesis that these omphacites crystallize in a highly ordered state.