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本文研究了江苏孟中榴辉岩富铝单斜辉石中出溶石榴子石现象，建立了出溶母体辉石成分，提出了出溶石榴子石的矿物反应。 相似文献
2.
石榴石辉石岩的单斜辉石中韭闪石和钛铁矿出溶结构及地质意义 总被引：10，自引：1，他引：10
本文首次报道了在苏鲁超高压变质带胡家岭地区石榴石辉石岩中发现的韭闪石出溶结构。该石榴石辉石岩是由石榴子石、单斜辉石以及镁铝尖晶石、钛铁矿和磁铁矿组成。在石榴子石巨斑晶中有单斜辉石包体，单斜辉石包体中又有石榴子石包体以及大量韭闪石出溶片晶和钛铁矿( 磁铁矿)出溶棒。单斜辉石中韭闪石出溶片晶呈平行条带状，其宽度在1～10μm之间。透射电子显微镜(TEM)观察韭闪石的(010)面平行于主晶透辉石的(010)面，且两者的界面在纳米尺度上是连续过渡的，证明韭闪石是出溶形成的。大量钛铁矿出溶棒的定向排列也显示出它们是自然出溶形成的。从单斜辉石出溶的矿物组合推测其原始单斜辉石成分中应富含H2O、Na和Ti，属高压型单斜辉石。该石榴石辉石岩经历了超高压变质作用后，在抬升减压过程中形成这些出溶结构。大量钛铁矿出溶棒均斜切韭闪石出溶片晶，表明该超高压岩石在减压过程中至少经历了两期以上导致温压明显变化的地质事件。 相似文献
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4.
徐淮地区镁铁质岩石捕虏体单斜辉石中石榴石和石英的出溶 总被引：7，自引：0，他引：7
徐淮地区早侏罗世侵入杂岩中榴辉岩,石榴辉石岩和单斜辉石岩捕虏体单斜辉石中可以观察丰富的出溶石英针和石榴石,黝帘石及角闪石的出溶叶片,榴辉岩中出溶石英针的绿辉石核部比其边部相对富含FeO和MgO,贫SiO2,Al2O3和CaO。在石榴辉石岩和单斜辉石岩捕虏体中具有出溶石榴石的单斜辉石。从靠近出溶石榴石的一侧向其核部,Al2O3,Na2O和TiO2含量降低,MgO,SiO2和CaO含量增加,单斜辉石中定向石英针的出溶表明曾经存在有超高压条件下（≥25×10^8Pa)稳定的过硅质绿辉石。单斜辉石中出溶石榴石表明温压条件的降低可能是引起出溶的一个主要原因,捕虏体中的矿物组合和岩相学特征表明它们曾经遭受了榴辉岩相和角闪岩相退化变质作用,这与因压力和温度降低引起矿物出溶的结果相吻合。 相似文献
5.
本文用电子背散射衍射技术(electron backscatter diffraction,EBSD)测试了海南文昌玄武岩中二辉橄榄岩包体中的辉石主晶与其出溶片晶的结晶学取向关系。结合电子探针成分测试,得出:单斜辉石(透辉石)主晶中出溶了两组不同方向的片晶,一组为斜方辉石(顽火辉石-易变辉石)片晶,另一组为单斜辉石(普通辉石)片晶。由于出溶片晶在EBSD测试切面上体现为以线状体,因此需要找到一种方法将线状体所代表的片晶的晶面符号推算出来。本文介绍了一种利用吴氏网进行坐标系旋转的"晶带相交法",该方法可以作图推算出溶片晶的晶面符号。根据"晶带相交法"得出,斜方辉石(顽火辉石-易变辉石)出溶片晶为(100),单斜辉石(普通辉石)出溶片晶为~(401)。根据前人的研究资料,出溶片晶~(401)可能指示最小出溶压力为9.5~12.5GPa。出溶片晶的结晶学取向涉及到主晶与出溶体的晶体结构匹配关系,并且与出溶温度-压力有关,因此出溶片晶的结晶学取向分析具有晶体化学理论意义和反映地质温压过程的实际意义。这种"晶带相交法"可以推广应用于其他矿物出溶结构的结晶学取向研究中。 相似文献
6.
西准噶尔白碱滩二辉橄榄岩中两种辉石的出溶结构及其地质意义 总被引：3，自引：11，他引：3
克拉玛依白碱滩尖晶石二辉橄榄岩主要由橄榄石、单斜辉石、斜方辉石和尖晶石组成,橄榄石和斜方辉石均发生程度不等的蛇纹石化。单斜辉石一般很新鲜。单斜辉石和斜方辉石均发育出溶结构,出溶条纹或者平直或者发生舒缓的弯曲变形(即便是在发生弯曲的情况下也是完全平行的)。透辉石-普通辉石出溶体一般呈针状(直径一般为1μm,长度>150μm),顽火辉石出溶条纹直径一般为1～3μm(长度>300μm)。斜方辉石主晶属于顽火辉石-易变辉石,单斜辉石主晶为透辉石(成分很均一)。地质温度压力估算表明,白碱滩二辉橄榄岩中辉石出溶结构发生的温度为700℃～1000℃、压力为2.0～2.7GPa,它们代表辉石出溶结构形成的最低PT条件。白碱滩二辉橄榄岩至少经历了三个演化阶段:原始辉石与尖晶石和橄榄石平衡共生(阶段Ⅰ,>94km);随着地幔上隆,原始辉石结构不稳定,分解并形成出溶结构(阶段Ⅱ,700℃～1000℃),斜方辉石开始分解的深度为94km,单斜辉石开始分解的深度为78km;之后,蛇绿岩经历的侵位事件导致辉石发生塑性变形(阶段Ⅲ)。蛇绿岩侵位之前,地幔岩曾发生了>50km的隆升,而且,在隆升过程中地幔岩没有发生明显部分熔融(地幔岩因此没有经历明显的岩浆抽提过程)。 相似文献
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从对固溶体中离子的扩散机制研究中发现：保温温度为773K－1023K时，斜方顽火辉石－正铁辉石固溶液中Fe^2 ，Mg^2 发生有序－无序扩散；扩散机制有两种类型：等价于spinadal分解机制或等价于“成核－生长”机制；并对扩散条件进行了探讨。 相似文献
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Howardites-Eucrite-Diogenite(HED)族陨石普遍被认为来自于灶神星,辉石颗粒中出溶片晶的形成是母体经历热变质事件的直接产物,因此出溶辉石的元素迁移规律可以反映灶神星经历的热变质条件。本文采用扫描电镜、激光拉曼光谱仪和电子探针对不同类型HED族陨石样品进行了分析。结果表明,HED族陨石中非平衡型辉石颗粒的Ca-Mg-Fe元素不均一,各样品中平衡型辉石颗粒的Ca-Mg-Fe元素平均扩散速率比值约为νCa∶νMg∶νFe=5∶1∶4,根据二辉石温度计得出母体热变质温度范围为700～1000℃,且玄武质Eucrite平衡辉石指示的温度普遍低于Howardites指示的温度,反映可能存在垂向压力差异性。这些特征都说明灶神星热变质期间的热源主要来源于演化早期玄武岩浆的快速喷发掩埋。 相似文献
9.
CCSD超高压变质岩绿辉石中的石英出溶体及其大陆动力学意义 总被引：2，自引：0，他引：2
单斜辉石中发育石英出溶体是UHP变质作用的典型矿物学标志之一,在世界上著名UHP变质地体中屡有发现。本文利用激光Raman光谱和电子探针分析在中国大陆科学钻探先导孔(CCSD-PP1)榴辉岩岩心的绿辉石中发现了大量石英(棒)出溶现象。通过与CCSD主孔榴辉岩各种赋存形式的绿辉石成分对比,发现含石英出溶体的绿辉石具有超硅特征,这是出溶现象发生的决定性因素之一。结合高压实验岩石学资料,提出在UHP变质的峰值期部分Si进入六次配位的Si-O八面体位置,压力降低这部分Si析出,形成石英出溶体的出溶机制。结合新的矿物学研究进展,认为绿辉石中出溶石英所标志的压力应远大于前人提出的2.5GPa,意味着苏鲁超高压变质带陆壳物质的俯冲深度要大于目前一般认为的80~120km范围。 相似文献
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利用拉曼光谱学和费氏台方法对若干地区超高压榴辉岩中柯石英和榴辉岩中石英出溶体的超显微构造特征进行了研究。研究结果表明，石榴石（或绿辉石）中柯石英向石英相变是一个连续变化过程。绿辉石中石英出溶体和主晶具有一定的晶体学拓扑关系，即石英出溶体长轴有两个展布方向：平行于绿辉石（100）裂理面和平行于绿辉石（－101）面。目前，部分学者推断榴辉岩绿辉石中石英出溶体可作为超高压变质作用的标志。笔者认为，棒状定向石英在绿辉石中出溶的温压条件和出溶机理尚未查明。因此，需加强过量二氧化硅单斜辉石出溶机理的超高压实验研究，从而为证实石英出溶体作为超高压标志提供实验定量约束。 相似文献
11.
M. A. Carpenter 《Contributions to Mineralogy and Petrology》1978,67(1):17-24
Omphacites with a range of compositions from the blueschist rocks of Syros, Greece and from included blocks in serpentinite from the Motagua fault zone, Guatemala, have been examined by transmission electron microscopy. The complex microstructures observed are all on a fine scale and are composed of exsolution and antiphase features. At least three different assemblages have been identified: (a) a single ordered phase with antiphase domains, (b) two exsolved phases, one ordered and the other disordered and (c) two exsolved phases, both apparently ordered. Selected area electron diffraction patterns provide evidence for P2/n, P2/c, and P2 space groups in different parts of the ordered crystals.The microstructures cannot all be readily explained in terms of a simple equilibrium phase diagram and some are attributed to alternative and metastable transformations. It is suggested that under the low temperature conditions of blueschist metamorphism, omphacite crystallised metastably below its ordering temperature with imperfect cation order. Subsequent development by cation ordering and exsolution was controlled by kinetics, the fastest available transformation being used to give reductions in free energy. Ordering preceded exsolution and may have occurred in a series of steps as predicted by the Ostwald step rule. Slight differences in composition and initial state of order locally influenced which reaction pathway was embarked upon and many of the products may be metastable. Such behaviour is apparently sensitive to thermal history. 相似文献
12.
南极拉斯曼丘陵长英质片麻岩中夕线石的出溶现象 总被引：2，自引：0，他引：2
南极拉斯曼丘陵长英质片麻岩中的粗粒夕线石可能有内部出溶现象,出溶形成的矿物有磁铁矿、钛铁矿-赤铁矿和石英出溶矿物条纹,并有少量的斜方辉石.电子探针成分分析表明,本区夕线石高温结晶时不仅有Fe3 ,可能还有Fe2 、Mg2 和Ti4 的替换,铁氧化物质量分数可高达2.9%;随着温度的不断降低,固溶体互溶度也不断减小,大部分微量组分从夕线石中析出形成出溶结构,而且低温变体中稳定的替换元素以Fd3 为主.铁组分的类质同像替换对物理化学计算和夕线石矿化环境均有所影响,对夕线石晶胞参数a的影响很小,而对b,尤其对c的影响较大,与前人的结论有所不同. 相似文献
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C. A. McCammon I. Jackson A. E. Ringwood J. D. Cashion 《Physics and Chemistry of Minerals》1984,11(4):182-193
(Fe, Mn)S and (Fe, Mg)S solid solutions are examined to study and compare the properties of Fe2+ in two different B1-structured hosts, and also to study the relative stability of the B1 (NaCl) and B8 (NiAs) structures at high pressure. The Mössbauer spectra of (Fe, Mn)S and (Fe, Mg)S B1 solid solutions are quadrupole doublets at 298 K with parameters which vary smoothly with Fe2+ concentration. At 4.2 K the Mössbauer spectra of (Fe, Mn)S and Fe-rich (Fe, Mg)S B1 solid solutions are magnetically split into eight lines, but the spectra of Mg-rich (Fe, Mg)S solid solutions are quadrupole doublets. The line widths of the magnetic spectra are broad, consistent with a multiaxial spin arrangement. Some properties of the hypothetical phase FeS(B1) are calculated from the solid solution data; the phase is inferred to be relatively ionic compared to FeS(B8) and has a molar volume that is 7.2 percent larger than the B8 phase at 298 K. The large inferred volume difference between FeS(B1) and FeS(B8) should cause exsolution of a B8-structured phase from (Fe, Mn)S and (Fe, Mg)S B1 solid solutions at high pressure. This behaviour is confirmed experimentally at high pressure using X-ray diffraction and Mössbauer spectroscopy, and the results are correlated with thermodynamic calculations of the phase boundaries based on estimates of the volume and free energy differences between the B1 and B8 phases of FeS derived from atmospheric pressure data. The absence of an increase in solubility of Mg and Mn in the B8 phase with pressure suggests that any polymorphism in MnS and MgS at high pressure is unlikely to involve the B8 phase. Shock wave data for MgO and Fe0.94O reported in the literature suggest similar behaviour in the system FeO-MgO at high pressure, namely exsolution of essentially pure FeO(hpp) from (Fe, Mg)O B1 solid solutions. 相似文献
14.
西藏羌塘地区榴辉岩石榴子石和磷灰石中均发育矿物出溶体,结合电子探针和扫描电镜分析及能谱分析,确定了石榴子石中的出溶体有金红石、石英和角闪石,指示其可能经历了高压/超高压变质作用。本研究在磷灰石中发现了金红石出溶,并认为其可能是在高压/超高压条件下元素相互置换的结果,置换方式为Ti~(4+)(Fe~(2+)、Si~(4+))=2Ca~(2+),这些出溶体的形成为榴辉岩曾经历高压/超高压变质作用提供了矿物学证据。 相似文献
15.
巨晶普通辉石的Ｍ１位分裂李一良，支霞臣，李玉芝，李铁，张裕恒（中国科学技术大学，合肥２３００２６）关键词巨晶辉石，Ｍ１位分裂，面积约束法，近邻边效应，Ｔ位铁单斜辉石的穆斯堡尔谱学研究历时已久。但由于其晶体结构和成份的复杂性、化学不均一性及出溶现象等［... 相似文献
16.
新疆阿尔泰可可托海3号伟晶岩脉重钽铁矿研究 总被引：1，自引：0，他引：1
重钽铁矿是主要见于高度分馏花岗伟晶岩中的一种罕见的钽矿物。新疆阿尔泰可可托海3号伟晶岩脉中存在的重钽铁矿呈他形，与钽猛矿(因Ta含量的明显差异可分为钽锰矿I和钽锰矿Ⅱ)和铀细晶石共生形成铌钽矿物集合体。钽锰矿I构成集合体的主体，而重钽铁矿与相对富Mn和Ta的钽锰矿Ⅱ紧密共生并分布在集合体的边部。重组铁矿的RTa[RTa＝Ta／(Nb Ta)]在0．96—0．99间变化，RMn[RMn＝Mn／(Fe Mn)]在0．10—0．2l间变化。铌钽铁矿的共生组合和化学成分特征表明，重钽铁矿是钽锰矿I在非平衡条件下快速结晶后残余亚稳定相出溶的产物。 相似文献
17.
Former idioblastic garnet crystals of an Archaean granulite with Mg/(Mg+Fe+Mn)-ratios (= M) near 0.40 were converted to symplectitic pseudomorphs consisting mainly of cordierite (M=0.61), orthopyroxene (M=0.40), and a relic garnet with a new composition (M=0.18), during a static metamorphism which is related in time to the Vredefort event. On the basis of experimental data for the continuous reaction garnet+quartz=orthopyroxene+cordierite the conditions of metamorphism were near 5 kb, 700 °C. Orthopyroxenes crystallized initially as minute, myrmekitic grains with metastable excess Al contents up to 13 mol% Al2O3 and, through grain growth and Al exsolution, transformed into dense aggregates of coarser crystals with equilibrated compositions near 3 mol% Al2O3. In the absence of free silica hercynitic spinel appears as an additional phase that coexists with cordierite, orthopyroxene, and garnet of more magnesian compositions than in the case of silica saturation.Pseudotachylite veins crosscutting the hornfelsed granulite consist of pyroxene of variable Al contents, two feldspars, opaques, and quartz, and are finely recrystallized. There is textural and mineral chemical evidence from both the Al-contents of the pyroxenes and the Mg/Fe distribution among the phases adjacent to the pseudotachylite that these veins were emplaced late during the static metamorphism, which was probably caused by a local, deep-seated magma diapir. On this basis, the meteorite impact hypothesis for the origin of the Vredefort Structure is considered less likely than a mechanism of internal origin which can be made responsible for the close link in time and space between static metamorphism and the high strain rate deformation that produced the pseudotachylite. 相似文献
18.
Olivine phenocrysts in microporphyritic xenoliths in the St. Mesmin chondrite (LL-breccia) show parallel rimward variations of FeO (10 to > -30wt.%), CaO (0·1–0·4%), MnO (0·2–0·8%) and Cr2O3 (0·2–0·7%). Aluminum is near background levels and does not vary systematically with iron. Titanium, sodium and nickel are below the limit of detection. Covariation of Fe and Cr in this olivine distinguishes it from the olivines in lunar mare basalts, in which Cr varies inversely with Fe.Transmission electron microscopy of the St. Mesmin olivine suggests that it is free of submicroscopic inclusions and exsolution lamellae and that the chromium present occurs in solid solution in the olivine. Charge balance and ionic radius considerations suggest that it occurs as Cr2+, whose effective ionic radius is nearly identical to that of Mn2+.The different Fe-Cr relationships observed in the lunar basaltic and St. Mesmin olivines reflect different crystallization sequences. Chromian spinel coprecipitated with olivine in the lunar basalts, reducing the activity of chromium in the melt and leading to the observed anticorrelation of Fe and Cr in olivine (butler, 1972). By contrast, olivine precipitated first in the St. Mesmin microporphyry and was the only solid phase present until more than half of the rock had crystallized. Parallel variation of Fe and Cr reflects crystallization from a melt in which the activity of chromium was increasing. 相似文献
19.
闪锌矿中杂质Fe存在形式的重新认识 总被引：5，自引：1，他引：5
闪锌矿作为一种重要的金属硫化物已得到广泛的研究，但在对闪上矿中杂质Ｆｅ存在形式的认识上却存在许多问题。本文对不同含Ｆｅ量的天然闪锌矿测定并分析了Ｆｅ的Ｋ边ＥＸＡＦＳ谱，同时对低温光吸收谱及穆斯堡尔进行了研究。结果表明，Ｆｅ在闪锌矿中主要以六配位形式存在。 相似文献
20.
Adriana Heimann Brian L. Beard Clark M. Johnson 《Geochimica et cosmochimica acta》2008,72(17):4379-4396
Highly differentiated igneous rocks can, in some cases, have 56Fe/54Fe ratios that are significantly higher than those of mafic- to intermediate-composition igneous rocks. Iron isotope compositions were obtained for bulk rock, magnetite, and Fe silicates from well-characterized suites of granitic and volcanic rocks that span a wide range in major- and trace-element contents. Sample suites studied include granitoids from Questa, N.M. (Latir volcanic field) and the Tuolumne Intrusive Series (Sierra Nevada batholith), and volcanic rocks from Coso, Katmai, Bishop Tuff, Grizzly Peak Tuff, Seguam Island, and Puyehue volcano. The rocks range from granodiorite to high-silica granite and basalt to high-silica rhyolite. The highest δ56Fe values (up to +0.31‰) are generally restricted to rocks that have high Rb (>100 ppm), Th (>∼15 ppm) and SiO2 (>70 wt.%) but low Fe (<2 wt.% total Fe as Fe2O3) contents. Magnetite separated from these rocks has high δ56Fe values, whereas Fe silicates have δ56Fe values close to zero. Although in principle crystal fractionation might explain the high δ56Fe values, trace-element ratios in high-δ56Fe igneous rocks indicate that crystal fractionation is an unlikely explanation. The highest δ56Fe values occur in volcanic and plutonic rocks that contain independent evidence for fluid exsolution, including sub-chondritic Zr/Hf ratios, suggesting that loss of a low-δ56Fe ferrous chloride fluid is the most likely explanation for the high δ56Fe values in the bulk rocks. Based on magnetite solubility in chloride solutions and predicted Fe isotope fractionations among Fe silicates, magnetite, and ferrous chloride fluids, the increase in δ56Fe values of bulk rocks may be explained by isotopic exchange between magnetite and , which predicts an increase in the δ56Fe values of magnetite upon fluid exsolution. This model is consistent with the δ56Fe values measured in this study for bulk rocks, as well as magnetite and Fe silicates. Our results suggest that fluid exsolution from siliceous hydrous magmas, which sometimes produce porphyry-style Cu, Mo, or Cu-Au mineralization, may be traced using Fe isotopes. 相似文献