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危地马拉目前已成为仅次于缅甸的第二大翡翠原料供应地。这两个产地翡翠辨别的需求愈发迫切,且应用意义较大。采用显微镜观察、电子探针分析及背散射电子照相获得危地马拉蓝水料翡翠的矿物成分及结构构造特征,结合两产地翡翠产出的大地构造环境、自然地理环境、原石特征与矿物成分特征等进行对比分析。总体上,危地马拉翡翠次生原石有一定的磨圆,呈次棱角状,“皮”(风化皮)厚度较薄,较少出现翻砂现象,由“皮”向里,极少甚至几乎不存在“红雾”。相对地,缅甸翡翠次生原石发育显著的球状风化,原石通常有较好的磨圆度,棱角状不明显,“皮”厚度可达数厘米,用手压磨有显著的翻砂现象, “皮”“肉”之间偶可见“红雾”。硬玉与绿辉石成分判别图显示危地马拉翡翠中硬玉和绿辉石呈相对富Ca、贫Na的特征,而缅甸翡翠中硬玉和绿辉石整体呈相对贫Ca、富Na的特征。在Fe含量上,危地马拉翡翠中硬玉的Fe含量较缅甸翡翠中硬玉的Fe含量偏低,而危地马拉翡翠中绿辉石的Fe含量较缅甸翡翠中绿辉石的Fe含量偏高。对翡翠外观特征的充分对比和对判别图的综合分析可应用于实际中翡翠产地的区分。 相似文献
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The present paper reports, for the first time, the occurrence of an omphacite‐bearing mafic schist from the Asemi‐gawa region of the Sanbagawa belt (southwest Japan). The mafic schist occurs as thin layers within pelitic schist of the albite–biotite zone. Omphacite in the mafic schist only occurs as inclusions in garnet, and albite is the major Na phase in the matrix, suggesting that the mafic schist represents highly retrogressed eclogite. Garnet grains in the sample show prograde‐type compositional zoning with no textural or compositional break, and contain mineral inclusions of omphacite, quartz, glaucophane, barroisite/hornblende, epidote and titanite. In addition to the petrographic observations, Raman spectroscopy and focused ion beam system–transmission electron microscope analyses were used for identification of omphacite in the sample. The omphacite in the sample shows a strong Raman peak at 678 cm?1, and concomitant Raman peaks are all consistent with those of the reference omphacite Raman spectrum. The selected area electron diffraction pattern of the omphacite is compatible with the common P2/n omphacite structure. Quartz inclusions in the mafic schist preserve high residual pressure values of Δω1 > 8.5 cm?1, corresponding to the eclogite facies conditions. The combination of Raman geothermobarometries and garnet–clinopyroxene geothermometry gives peak pressure–temperature (P–T) conditions of 1.7–2.0 GPa and 440–540 °C for the mafic schist. The peak P–T values are comparable to those of the schistose eclogitic rocks in other Sanbagawa eclogite units of Shikoku. These findings along with previous age constraints suggest that most of the Sanbagawa schistose eclogites and associated metasedimentary rocks share similar simple P–T histories along the Late Cretaceous subduction zone. 相似文献
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Dehydration experiments on natural omphacites: qualitative and quantitative characterization by various spectroscopic methods 总被引：1，自引：0，他引：1
M. Koch-Müller I. Abs-Wurmbach D. Rhede V. Kahlenberg S. Matsyuk 《Physics and Chemistry of Minerals》2007,34(9):663-678
A series of natural omphacites from a wide range of P, T occurrences were investigated by electron microprobe (EMP), infrared (IR)-, Mössbauer (MS)- and optical spectroscopy in the UV/VIS spectral range (UV/VIS), secondary ion mass spectrometry (SIMS) and single crystal structure refinement by X-ray diffraction (XRD) to study the influence of hydrogen loss on valence state and site occupancies of iron. In accordance with literature data we found Fe2+ at M1 as well as at M2, and in a first approach assigned Fe3+ to M1, as indicated by MS and XRD results. Hydrogen content of three of our omphacite samples were measured by SIMS. In combination with IR spectroscopy we determined an absorption coefficient: ε i,tot = 65,000 ± 3,000 lmolH2O ?1 cm?2. Using this new ε i,tot value, we obtained water concentrations ranging from 60 to 700 ppm H2O (by weight). Hydrogen loss was simulated by stepwise heating the most water rich samples in air up to 800°C. After heat treatment the samples were analyzed again by IR, MS, UV/VIS, and XRD. Depending on the type of the OH defect, the grade of dehydration with increasing temperature is significantly different. In samples relatively poor in Fe3+ (<0.1 Fe3+ pfu), hydrogen associated with vacancies at M2 (OH bands around 3,450 cm?1) starts to leave the structure at about 550°C and is completely gone at 780°C. Hydrogen associated with Al3+ at the tetrahedral site (OH bands around 3,525 cm?1, Koch-Müller et al., Am Mineral, 89:921–931, 2004) remains completely unaffected by heat treatment up to 700°C. But all hydrogen vanished at about 775°C. However, this is different for a more Fe3+-rich sample (0.2 Fe3+ pfu). Its IR spectrum is characterized by a very intense OH band at 3,515 cm?1 plus shoulder at 3,450 cm?1. We assign this intense high-energy band to vibrations of an OH dipole associated with Fe3+ at M1 and a vacancy either at M1 or M2. OH release during heating is positively correlated with decrease in Fe2+ and combined with increase in Fe3+. That dehydration is correlated with oxidation of Fe2+ is indirectly confirmed by annealing of one sample in a gas mixing furnace at 700°C under reducing conditions keeping almost constant OH? content and giving no indication of Fe2+-oxidation. Obtained data indicate that in samples with a relatively high concentration of Fe2+ at M2 and low-water concentrations, i.e., at a ratio of Fe2+ M2/H > 10 dehydration occurs by iron oxidation of Fe2+ exclusively at the M2 site following the reaction: \( {\left[ {{\text{Fe}}^{{{\text{2 + [ M2]}}}}{\text{OH}}^{ - } } \right]} = {\left[ {{\text{Fe}}^{{{\text{3 + [ M2]}}}} {\text{O}}^{{{\text{2}} - }} } \right]} + {\text{1/2}}\;{\text{H}}_{{\text{2}}} \uparrow . \) In samples having relatively low concentration of Fe2+ at M2 but high-water concentrations, i.e., ratio of Fe2+ M2/H < 5.0 dehydration occurs through oxidation of Fe2+ at M1. 相似文献
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Petrogeneses of impure dolomitic marble and enclosed eclogite from the Xinyan area, Dabie ultrahigh-pressure (UHP) metamorphic terrane, central China were investigated with a special focus on fluid characteristics. Identified carbonate-bearing UHP assemblages are Dol + Coe ± Arg (or Mgs) ± Ap, Dol + Omp ± Coe ± Ap ± Arg (or Mgs), Phen + Omp + Coe + Dol ± Arg and Dol + Coe + Phen + Rt ± Omp ± Arg ± Ap. Retrograde assemblages are characterized by symplectitic replacement of Tr–Ab and Di–Ab after omphacite, and Phl–Pl symplectite after phengite. The P–T conditions of UHP metamorphism were estimated to be P > 2.7 GPa and T > 670 °C by the occurrence of coesite inclusions in garnet in enclosed eclogite and garnet–clinopyroxene geothermometer. The P–T conditions of initial amphibolitization were estimated to be 620 < T < 670 °C and 1.1 < P < 1.3 GPa by calcite–dolomite solvus thermometer and mineral parageneses. Phase relations in P–T– X CO 2 space in the systems NaAl–CMSCH and KCMASCH were calculated in order to constrain fluid compositions. Compositions and parageneses of UHP-stage minerals suggest the presence of fluid in UHP and exhumation stages. Occurrence of retrograde low-variance assemblages indicates that fluid composition during amphibolitization was buffered. A metastable persistence of magnesite and very restricted occurrence of calcite, magnesite and dolomite suggest a low fluid content in the post-amphibolitization stage. 相似文献
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榴辉岩中绿辉石的测定方法研究 总被引：3，自引：0，他引：3
通过对某地榴辉岩中伴生的有用矿物的纯矿物物质组成的研究,发现Ｎａ可作为其中绿辉石的特征性成分,且Ｎａ２Ｏ含量与其纯度呈正相关。因此,推荐用测定Ｎａ２Ｏ量并以求得的换算系数计算榴辉岩中绿辉石含量的化学物相分析方法。经合成样品验证,方法的相对误差＜１．７％,用于生产样品分析,所得结果的重现性好,平均偏差＜０．５％。 相似文献
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A ternary solid solution model for omphacite with the end-members jadeite (NaAlSi2 O6 ), diopside (CaMgSi2 O6 ) and hedenbergite (CaFeSi2 O6 ) 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+H2 O±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). 相似文献
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Aragonite and omphacite-bearing metapelite occurs in the albite–biotite zone of the Togu (Tohgu) area, Besshi region, Sambagawa metamorphic belt, central Shikoku, Japan. This metapelite consists of alternating graphite-rich and graphite-poor layers that contain garnet, phengite, chlorite, epidote, titanite, calcite, albite, and quartz. A graphite-poor layer contains a 1.5-cm ivory-colored lens that mainly consists of phengite, calcite, albite, and garnet. Aragonite, omphacite, and paragonite occur as inclusions in the garnet of the ivory lens. The aragonite has a composition that is close to the CaCO3 end-member: the FeCO3 and MnCO3 components are both less than 0.3 mol% and the SrCO3 component is about 1 mol%. The aragonite + omphacite + quartz assemblage in garnet indicates equilibrium conditions of P > 1.1–1.3 GPa and T = 430–550°C. Quartz grains sealed in garnet of the aragonite and omphacite-bearing sample and other metapelites in the Togu area preserve a high residual pressure that is equivalent to the Sambagawa eclogite samples. These facts suggest that: (i) the Togu area experienced eclogite facies metamorphism; and (ii) thus, eclogite facies metamorphism covered the Sambagawa belt more extensively than previously recognized. 相似文献
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