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1.
安徽省泗县山头地区分布着金刚石砂矿,其金刚石来源一直存在争议,尤其是在安徽省宿州栏杆地区发现了碱性基性岩型的金刚石后,一些学者认为栏杆地区可能是砂矿的来源.本文对山头金刚石砂矿中指示矿物(石榴子石和铬铁矿)进行了电子探针分析,结果显示石榴子石矿物化学式A32+B23+(SiO4)3中的A主要由Mg2+、Fe2+和Ca2+离子占位,B主要由Al3+离子和少量的Mn3+离子占位,以铁铝榴石(Alm)为主,其次是镁铝榴石(Pyp),属于铁铝-镁铝-钙铝石榴子石系列的G3、G4石榴子石;铬铁矿中Cr2O3的含量绝大多数大于40 wt％,MgO的含量平均在8 wt％左右,TiO2含量在0.11～2.26 wt％之间,属于中铬-铬铁矿,与山东、辽宁金伯利岩中发现的中铬-铬铁矿成分基本一致,说明其物源并非来自栏杆地区碱性基性岩型金刚石原生矿. 相似文献
2.
关于云母族矿物的红外光谱研究,国内外一些学者曾做过不少工作。笔者就近年来所收集到的一些产自宁芜地区、南岭地区花岗岩类岩石中27个黑云母样品,进行了红外光谱测定,确定了某些特征吸收峰的偏移及其与化学组分之间的关系,并探讨了黑云母矿物中主要金属阳离子的相互置换和晶体结构的关系。 黑云母属三八面体型的2∶1层状结构硅酸盐矿物。结构中上下四面体片(T)以尖顶相对,中间夹氢氧镁石型[Mg—O_4(OH)_2]八面体片(O),构成T—O—T型结构层。占有四面体晶位的阳离子主要为Si,约有1/4的Si可被R~(3+)(主要为Al~(3+)、次为Fe~(3+))取代。占有八面体晶位的阳离子主要为Mg~(2+)或Fe~(2+),次为Fe~(3+)、Al~(3+)、Mn~(2+)等。由T—O—T所组成的结构层则通过层间大阳离子K~+(少量的Na~+、Ca~(2+)等)彼此相连接。结构 相似文献
3.
辽宁瓦房店金刚石矿区金伯利岩中的石榴石一直被当作镁铝榴石。为了确定矿区颜色复杂的石榴石种类,本文对矿区的石榴石进行了系统的采样分析,测定了112件石榴石样品的晶胞参数、50件样品的微区化学成分和40件样品的红外光谱。利用石榴石晶胞参数、红外光谱、化学成分和化学分子式方法对矿区石榴石进行分类,结果显示:晶胞参数分类法误差大,容易得出错误结论;红外图谱分类法准确度不高,只能作为参考方法;化学成分分类法太过笼统,达不到详细划分石榴石种类的目的;化学分子式分类法可把矿区的石榴石详细划分6个矿种:镁钙铁-铝铬铁榴石、镁铁钙-铝铬铁榴石、镁钙铁-铝铬榴石、镁钙-铝铬铁镁榴石、镁铁钙-铝铬榴石、镁铁钙-铝铁铬榴石,每种石榴石都充分反映了A、B离子的种类及占位特征,是4种分类方法中最为科学的方法。研究认为瓦房店金刚石矿区金伯利岩中石榴石A端元成分以Mg2+离子占位为主;B端元成分以Al3+离子占位为主。由于阳离子替代普遍,A、B端元成分复杂,瓦房店金伯利岩中不存在单纯意义上的镁铝榴石。 相似文献
4.
电气石岩——一种和矿化有关的岩石类型 总被引：7，自引：2，他引：7
电气石是一种复杂的含水、氟、氯硅酸盐矿物族,其一般分子式为WX_3Y_6(BO_3)_3Si_3O_(18)(OH,F,Cl),其中W=Na~+、Ca~(2+)、K~+,X=Al~(3+)、Fe~(3+)、Fe~(2+)、Li~+、Mg~(2+)、Mn~(2+),Y=Al~(3+)、Fe~(3+)、Cr~(3+)、V~(3+)。该矿物族存在许多端员矿物,如黑电气石、镁电气石和钙镁电气石等。电气石在很大范围的温压条件下稳定,故其可提供有关岩浆或流体的一些信息,如P、T、fo_2、α_(H_2O)、α_(F)~-、Mg/(Mg+Fe)比值等(Plimer,1988);同时该矿物类质同象替换十分复杂,其常量元素组成可提供其形成的地质体系化学组成的线索,Henry和Guidotti(1985)在Al-∑Fe-Mg和Ca-∑Fe-Mg三角图解上确定了不同类型岩石中电气石的特定区域。电 相似文献
5.
《矿物学报》2013,(3)
本文对荷花坪锡多金属矿,锡田锡钨多金属矿以及新田岭钨矿矽卡岩中的石榴子石样品分别进行了主量元素、微量元素及红外光谱测定。结果表明,3种矽卡岩中的石榴子石多数属于(铁铝榴石+镁铝榴石+锰铝榴石)<15%的钙铁-钙铝榴石系列。新田岭钨矿的石榴子石中钙铁榴石端员含量明显高于其他两个锡矿。此外,在荷花坪、新田岭矿区发现了与后期铅锌矿化有关的锰质石榴子石。在单矿物尺度上,荷花坪矿区石榴子石核部富集钙铝榴石,边部富集钙铁榴石,而锡田矿区石榴子石与之相反;新田岭矿区石榴子石具有相对均匀的核部而边部发育细密的振荡环带。在稀土配分模式上,荷花坪矿区石榴子石重稀土富集,轻稀土亏损,δEu负异常较弱;锡田矿区石榴子石稀土总量最高,轻重稀土无明显分异,δEu负异常较弱;新田岭矿区石榴子石轻重稀土分异极强,重稀土富集,轻稀土严重亏损,δEu具显著的正异常。3种石榴子石的红外漫反射光谱均显示有10种吸收峰,其中低频区的5种与石榴子石成分中的钙铁榴石含量直接相关,因而造成新田岭矿区石榴子石的吸收峰与另两矿区石榴子石相比显著向低频波段移动。通过对华南3类含钨锡矽卡岩中的石榴子石的研究,确认了石榴子石的形成与矽卡岩形成中热液体系的环境变化密切相关。微量元素分析与红外光谱技术作为近年来矽卡岩型石榴子石研究的热点,能够提供传统研究中所不能涉及的微观信息。 相似文献
6.
本文收集了一组钛榴石样品,作了穆斯堡尔谱和化学分析。采用各对应双峰等值限制拟合。拟合结果,统计误差X~2均较小。文中还分析了钛榴石结构的阳离子占位情况,并对其五对双峰谱指派如下:Fe~(3+)在[Y]位和(Z)位,Fe~(2+)在{X}和[Y]位,而另一对双峰指派为Fe~(2+){X}→Fe~(3+)(Z)的电荷离域。从化学分析和穆斯堡尔谱数据求出二种方法Fe~(2+)/∑Fe的差值,说明钛榴石中有Ti~(3+)的存在,用此简便方法估算了Ti~(3+)的含量,得出了四面体中阳离子的占位择优为Fe~(3+)>(Al~(3+),Ti~(4+))的结论。 相似文献
7.
石榴石族是一种广泛分布的造岩矿物。分子式为:R_3~2+R_2~3+Si_3O_(12),其中R~(2+)=Ca、Fe~(2+)、Mg、Mn……,R~(3+)=Al、Fe~(3+)、Cr等。地质上常见的是两个系列,即:铝榴石系列(镁铝榴石、铁铝榴石、锰铝榴石)与铬钙铁榴石系列(钙铬榴石、钙铝榴石、钙铁榴 相似文献
8.
滇西北铜厂沟Mo-Cu矿床成矿流体和成矿物质来源:矽卡岩矿物学与稳定同位素证据 总被引：4，自引：1，他引：3
义敦地体位于三江特提斯成矿域中北段,晚三叠世和晚白垩世斑岩-矽卡岩型Mo-Cu多金属成矿作用强烈。铜厂沟Mo-Cu矿床位于义敦地体最南端,是近年来该区新探明的Mo-Cu矿床之一,已探明资源量142.5Mt。矽卡岩在铜厂沟矿区广泛出露,是该矿区最主要的赋矿岩石。根据矿物组合及共生关系,可将矽卡岩划分为石榴子石矽卡岩、透辉石矽卡岩和透闪石矽卡岩三种类型。通过详细的地质填图和钻孔岩心编录,发现铜厂沟矿区矽卡岩矿物组合受花岗闪长斑岩体与大理岩空间分布的控制:(1)由大理岩向外依次发育透辉石矽卡岩→透闪石矽卡岩→石榴子石矽卡岩;(2)由浅至深,石榴子石粒度逐渐变大;③矿化与透闪石、绿帘石等退化蚀变矿物密切相关,矿体多形成于外接触带。矽卡岩中最主要的矿物是石榴子石,多呈自形粒状或粒状集合体产出,颜色较深,均质性,以钙铝榴石为主(62.2%~78.3%),其次为钙铁榴石(16.7%~34.2%),少量锰铝榴石、铁铝榴石和镁铝榴石,属于钙铝榴石-钙铁榴石固溶体系列(Gro62-78And17-34Spe+Pyr+Alm2-6)。石榴子石Fe~(2+)/Fe~(3+)比值变化范围为0.00~0.20,平均值为0.06,指示石榴子石形成于酸性的氧化环境。石榴子石的δ~(18)OSMOW变化范围为5.2‰~9.5‰,反映矽卡岩可能直接继承斑岩体的氧同位素组成;金属硫化物具有较为均一的S-Pb同位素范围(δ~(34)S(CDT)=-0.7‰~1.4‰;~(206)Pb/~(204)Pb=18.332~18.694,~(208)Pb/~(204)Pb=38.454~39.088,~(207)Pb/~(204)Pb=15.588~15.663),表明成矿流体和成矿物质均来源于壳源的长英质岩浆。 相似文献
9.
湖南沅江是我国砂矿金刚石的重要产地,石榴子石和金刚石是砂矿中常见的重矿物,与金刚石相关的石榴子石特征研究,对揭示湖南砂矿金刚石的来源与形成条件有重要意义。本文随机选取湖南沅江辰溪地区金刚石砂矿中160粒碎屑石榴子石和5粒金刚石包裹体中的石榴子石,采用矿物学、地球化学并借鉴统计学方法对它们进行了分析比较。结果显示,碎屑石榴子石主要为铁铝-锰铝榴石系列,其中个别石榴子石含有金刚石包裹体。聚类分析、线性判别、逻辑回归分析计算显示,部分G3榴辉岩型石榴子石与金刚石可能具有成生联系。同时,两个采集地点的石榴子石类型、主微量元素具有一定的差异,其中一个地点的石榴子石样品DJZ-7-1具有与金刚石更强的亲缘性。基于本文碎屑石榴子石Si值大于3.02以及前人对湖南金刚石限定的温压条件进行分析,认为湖南金刚石可能形成于深度小于220 km的橄榄岩-榴辉岩混杂区,该区域系钾镁煌斑岩型金刚石来源的优势区域。据此,建议可在辰溪赤岩村河段上游区域进一步寻找幔源G3型石榴子石以及钾镁煌斑岩,以期发现原生金刚石矿床。 相似文献
10.
11.
A. Katerinopoulou A. Katerinopoulos P. Voudouris A. Bieniok M. Musso G. Amthauer 《Mineralogy and Petrology》2009,95(1-2):113-124
Unusual Ti–Cr–Zr-rich garnet crystals from high-temperature melilitic skarn of the Maronia area, western Thrace, Greece, were investigated by electron-microprobe analysis, powder and single-crystal X-ray diffraction, IR, Raman and Mössbauer spectroscopy. Chemical data showed that the garnets contain up to 8 wt.% TiO2, 8 wt.% Cr2O3 and 4 wt.% ZrO2, representing a solid solution of andradite (Ca3Fe3+ 2Si3O12 ≈46 mol%), uvarovite (Ca3Cr2Si3O12 ≈23 mol%), grossular (Ca3Al2Si3O12 ≈10 mol%), schorlomite (Ca3Ti2[Si,(Fe3+,Al3+)2]O12 ≈15 mol%), and kimzeyite (Ca3Zr2[Si,Al2]3O12 ≈6 mol%). The Mössbauer analysis showed that the total Fe is ferric, preferentially located at the octahedral site and to a smaller extent at the tetrahedral site. Single-crystal XRD analysis, Raman and IR spectroscopy verified substitution of Si mainly by Al3+, Fe3+ and Ti4+. Cr3+ and Zr4+ are found at the octahedral site along with Fe3+, Al3+ and Ti4+. The measured H2O content is 0.20 wt.%. The analytical data suggest that the structural formula of the Maronia garnet can be given as: (Ca2.99Mg0.03)Σ=3.02(Fe3+ 0.67Cr0.54Al0.33Ti0.29Zr0.15)Σ=1.98(Si2.42Ti0.24Fe0.18Al0.14)Σ=2.98O12OH0.11. Ti-rich garnets are not common and their crystal chemistry is still under investigation. The present work presents new evidence that will enable the elucidation of the structural chemistry of Ti- and Cr-rich garnets. 相似文献
12.
江西永平铜矿矽卡岩矿物特征及其地质意义 总被引：4，自引：3，他引：1
永平铜矿含矿岩石主要为绿帘石透辉石石榴石矽卡岩,这种岩石类型是与斑岩体有关的矽卡岩铜矿的典型赋矿岩石。通过对这一主要赋矿矽卡岩的研究,我们发现石榴石生长分为两个阶段:(1)早期石榴石:主要分布在石榴石颗粒核部,XAdr=1.0,主要以钙铁榴石为主,说明早期流体中可能含有较多的铁,是在较氧化条件下形成的;(2)晚期石榴石,沿石榴石裂隙重新成核或者在靠近流体通道的早期石榴石表面生长,出现震荡环带,XAdr=0.46~0.99,为钙铁-钙铝石榴石系列。石榴石发生变化的期间也形成新的矿物,如绿帘石、萤石、方解石和石英等。共存石榴石和绿帘石矿物中存在Fe3+-Al3+之间的替代,说明流体的氧逸度、组分浓度或aFe3+/aAl3+可能发生了变化。金属矿物也可能是在这一阶段形成的。永平铜矿矽卡岩从接触带到大理岩空间上有分带现象。从岩体到围岩的变化趋势为:石榴石含量减少,颜色存在红棕色-棕色-棕绿色-黄绿色-浅黄色的变化趋势;矿石品位降低,这与石榴石中Al2O3含量的变化较一致。我们认为这种变化是含矿热液对早期矽卡岩进行再交代改造的结果,表现为石榴石和绿帘石中Fe3+-Al3+含量的变化,并将Cu等金属沉淀下来。根据矽卡岩矿物的这些特征,在矿床勘探时,可依据棕色石榴石来追踪主矿体的位置。 相似文献
13.
Coexisting garnets and ilmenites have been synthesized at high pressure (21–40 kb) within the temperature range between 900 and 1100 °C from pyrolite-less-40% olivine and olivine basanite with various water contents. The two compositions yield phases with a range in the 100 Mg/Mg+Fe ratio for both garnet (41–76) and ilmenite (15–47). The distribution coefficient for iron and magnesiaum (K D(Fe, Mg) ilm-ga = 4.0±0.5) for coexisting phases does not appear to vary with change in the bulk composition or temperature of synthesis. The synthesized ilmenites are of similar composition to those of kimberlites in 100 Mg/Mg+Fe ratio and Al2O3 and Cr2O3 solid solution. Cr2O3 content in ilmenite is dependent on Cr2O3 in the bulk composition and also on Fe2O3 content of ilmenite. Fe2O3 content of ilmenite is very sensitive to f O2 and natural ilmenites from peridotites have formed under low f O2. Al2O3 solid solution in ilmenite as well as TiO2 in coexisting garnet tend to be higher with higher temperature. All the variety of compositions of ilmenites from kimberlites may be obtained from rocks rather close in composition to those used in experiments, within the same range of pressure and temperature but at variable oxygen fugacities. 相似文献
14.
Gianluca Iezzi Tiziana Boffa-Ballaran Catherine McCammon Falko Langenhorst 《Physics and Chemistry of Minerals》2005,32(3):197-207
Germanate garnets are often used as isostructural analogues of silicate garnets to provide insight into the crystal chemistry and symmetry of the less accessible natural garnet solid solutions. We synthesised two series of germanate garnets at 3 GPa along the joinVIIICa3VI(CaGe)IVGe3O12–VIIICa3VIFe2IVGe3O12 at 900 °C and 1,100 °C. Samples with compositions close to the CaGeO3 end-member consist of tetragonal garnet with a small amount of triclinic CaGe2O5. Samples with nominal compositions between XFe=0.4 and 1.0 consist of a mixture of tetragonal and cubic garnets; whereas, single-phase cubic garnets were obtained for compositions with XFe>1.2 (XFe gives the iron content expressed in atoms per formula unit, and varies between 0 and 2 along the join). Run products which were primarily single-phase garnet were investigated using Mössbauer spectroscopy. Spectra from samples synthesised at 1,100°C consist of one well-resolved doublet that can be assigned to Fe3+ in the octahedral site of the garnet structure. A second doublet, present primarily in samples synthesised at 900°C, can be assigned to Fe2+ at the octahedral sites of the garnet structure. The relative abundance of Fe2+ decreases with increasing iron content. Transmission electron microscopy analyses confirm this tendency and show that the garnets are essentially defect-free. The unit-cell parameters of tetragonal VIIICa3VI(CaGe)IVGe3O3 garnet decrease with increasing synthesis temperature, and the deviation from cubic symmetry becomes smaller. Cubic garnets show a linear decrease of unit-cell parameter with increasing iron content. The results are discussed in the context of iron incorporation into VIIIMg3VI(MgSi)IVSi3O3 majorite. 相似文献
15.
N. P. Laverov S. V. Yudintsev T. S. Livshits S. V. Stefanovsky A. N. Lukinykh R. C. Ewing 《Geochemistry International》2010,48(1):1-14
Complex oxides of the pyrochlore (space groups Fd3m, [8]A2
[6]B2O7) and garnet (Ia3d, [8]A3
[6]B2
[4]T3O12) structures (“A” = Ca2+, Ln3+/4+, An3+/4+; “B” = (Ti, Sn, Hf, and Zr)4+ in pyrochlore, and Al3+, Ga3+, and Fe3+ in garnet alone; “T” = (Al3+, Ga3+, and Fe3+) are promising matrices for actinide-bearing wastes. In order to identify optimal compositions of these phases, their isomorphic
capacity with respect to REE, actinides, and other components of wastes was examined. The long-term behavior of the matrix
at a repository was predicted based on data obtained on the behavior of pyrochlores and garnets under ion irradiation and
244Cm decay and on the determined leaching rates of REE from the matrices because of their interaction with aqueous solutions,
including that after amorphization. In order to propose efficient synthesis techniques, samples prepared with the use of various
methods were studied. The possibility of incorporating long-lived decay products of 99Tc into the crystalline matrices was analyzed. 相似文献
16.
This paper gives an analytical overview of the experimental data obtained by different authors at high P and T in the model system MgO–Al2O3–SiO2–Cr2O3 (MASCr). A set of four simple polynomial equations is proposed for the temperature and pressure dependence of chromium content in garnet and spinel in the assemblage Gar + Opx + Es and Gar + Fo + Opx + Sp.From the first equation, one can estimate the minimum pressure at a given temperature which is required for the formation of peridotite garnets of uncertain paragenesis with a known knorringite content. A combination of the second and third equations helps estimate P and T from the chromium content of garnet and spinel from assemblages containing both minerals. If the spinel composition is unknown, but there is reason to assign garnet to a spinel-bearing paragenesis, the fourth equation is applicable for estimating pressure at given temperature.Originally, the proposed garnet–spinel geothermobarometer was developed for a harzburgite paragenesis. However, it is applicable to garnets with CaO/Cr2O3 < 0.903 (including lherzolitic ones), that is, those within the Pyr–Kn–Uv triangle of the reciprocal quaternary diagram Pyr–Cros–Uv–Kn.Using the above equations and an empirical PCG geobarometer (Grütter et al., 2006), comparative geothermobarometric estimates were obtained for a set of garnet and garnet–spinel inclusions in diamonds and intergrowths with diamond, as well as garnet inclusions in spinel. If garnet has CaO/Cr2O3 = 0.35–0.40, the results are in good accord. For Cr-richest and Ca-poorest garnets, the PCG barometer shows pressures 10–15% higher compared with our estimates. 相似文献
17.
The rare garnet end member calderite, Mn 3 2+ Fe 2 3+ Si3O12, has been synthesized, under the oxygen fugacity of the hematite/magnetite buffer, at pressures not lower than 22 kbar. The synthetic crystals are generally zoned and may contain up to 3 mol% of the Fe2+-(=skiagite-) or 10 mol% of the Mn3+-(=blythite-) end members, but, under equilibrium conditions, the stable garnets have a restricted compositional range with about 1–4 mol% skiagite. Mn3+ represents only a residue of the Mn2O3 used in the starting material. At temperatures above 720° C (at 24 kbar) to 850° C (at 30 kbar) these garnets break down into coexisting pairs of magnetite-jacobsite and pyroxmangite-FeSiO3 solid solutions. No indication for divariancy of this breakdown reaction could be established so that the observed coexistence of garnet and breakdown products over a PT interval must be due to disequilibrium. Although extrapolations of the high-pressure stability data towards lower pressures are hazardous, it is clear that nearly pure calderite garnets can only form in metamorphic environments characterized by geothermal gradients not exceeding some 10°–15° C/km, that is in subduction zone metamorphism. A low-pressure end of the calderite stability is likely because, at temperatures below 250°–300° C, pyroxmangite probably becomes unstable and hydrous Mn2+-silicates appear among the low-temperature breakdown products of calderite. Since the upper temperature stability limits of the common garnet end members spessartine and andradite lie some 800° C above that for calderite, solid solutions with these components will drastically stabilize the garnet phase towards both higher temperatures and lower pressures. This explains why garnets containing around 70 mol% calderite can be formed in amphibolitefacies metamorphism. 相似文献
18.
Ferric iron in mantle-derived garnets 总被引：4，自引：0，他引：4
Robert W. Luth David Virgo Francis R. Boyd Bernard J. Wood 《Contributions to Mineralogy and Petrology》1990,104(1):56-72
The oxidation state of a mantle assemblage may be defined by heterogeneous reactions between oxygen and iron-bearing minerals. In spinel lherzolites, the presence of Fe3+ in spinel allows use of the assemblage olivine-orthopyroxene-spinel to define f
O
2 at fixed T and P. As a first step towards establishing an analogous reaction for garnet lherzolites, garnets from mantle-derived xenoliths from South Africa and the USSR have been analyzed with 57Fe Mössbauer spectroscopy at 298 and 77K to determine Fe3+/Fe2+ and the coordination state of iron. Garnets from South African alkremites (pyrope+Mg-spinel) and eclogites, as well as garnet-spinel and low-temperature garnet lherzolites from both South Afica and the USSR, have Fe3+/Fe<0.07. In contrast, garnets from high-temperature garnet lherzolites from within the Kaapvaal craton of South Africa have Fe3+/Fe>0.10. Ferric iron is octahedrally coordinated, and ferrous iron is present in the dodecahedral site in all samples. The occurrence of significant Fe3+ in these garnets necessitates caution in the use of geothermometers and geobarometers that are applied to mantle samples. For example, the presence of 12% of the Fe as Fe3+ in garnets can increase temperatures calculated from existing Fe/Mg geothermometers by>200°C. The concomitant increase in pressures calculated from geobarometers that use the Al content in orthopyroxene coexisting with garnet are 10–15 kbar. Results of calculations based on heterogeneous equilibria between garnet, olivine, and pyroxene are consistent with the derivation of the peridotite samples from source regions that are relatively oxidized, between the f
O
2 of the FMQ (quartz-fayalite-magnetite) buffer and that of the WM buffer. No samples yield values of f
O
2 as reduced as IW (iron-wüstite buffer). 相似文献
19.
Petr Gadas Milan Novák Dominik Talla Michaela Vašinová Galiová 《Mineralogy and Petrology》2013,107(2):311-326
Five distinct paragenetic, morphological and compositional types of grossular garnet (G1, G2, G3, G4, G5) were distinguished within the individual (sub)units of the zoned leucotonalitic pegmatite cutting serpentinized lherzolite with rodingite dikes at ??ár near Ruda nad Moravou, Staré Město Unit, Northern Moravia. Detailed study using Electron Microprobe Analysis, Laser Ablation Inductively Coupled Plasma Mass Spectrometry, Cathodoluminiscence and Infrared Spectroscopy revealed distinct compositional trends in major, minor and trace elements. The contents of Fe3+, Mn, Mg and Ti increase from early garnet (G1) in the outermost grossular subunit through the interstitial garnet (G2) in the leucocratic subunit to graphic intergrowths of quartz+garnet (G3) in the coarse-grained unit. Then these constituents decrease in inclusions of garnet (G4) from the blocky unit and large crystals of garnet (G5) from the quartz core. Some trace elements (V, Ni, Y) exhibit the same trends, only Be evidently increases in garnet from border zone to the centre. Fluorine has negative correlation with Fe3+ as well as some trace elements (Ta, Pb). Concentrations of H2O in garnets, up to 0.22 wt.% H2O, are comparable with spessartine-almandine garnets from the Rutherford No. 2 pegmatite, Virginia, and grossular garnets from high-temperature calc-silicate rocks (skarns). Water contents correlate positively with Fe3+, but inversely with F. The use of water contents in garnet to elucidate the fluctuations of activity of H2O during the pegmatite formation is only limited; the incorporation of hydrous defects seems to be controlled instead by crystal-structural constraints. However, the sum of all volatile components (H2O + F) increases about twice from the outermost subunit to the centre of the pegmatite body. 相似文献
20.
Most of the Al3+ entering the pyroxenes does so by substituting for tetrahedral Si4+. This creates a charge imbalance that requires the simultaneous entry of Cr3+, Ti4+, Fe3+ or Al3+ into octahedral sites. Cr3+, because of its high crystal field stabilisation energy (CFSE), is the most important of these elements to enter the early-formed pyrosenes but it is replaced by Ti4+ later in fractionation when the Cr3+ content of the melt becomes depleted. The dependence of Cr3+ and Ti4+ on charge balance controls their partition between coexisting pyroxenes and olivines. Ca-rich pyroxene which contains more Al3+ than Ca-poor pyroxene also has more Ti4+ and Cr3+ whereas olivine, which contains negligible Al3+, has low Cr3+ and Ti4+. The Al3+ content of pyroxenes is influenced by changes in P, T, \(a_{{\text{SiO}}_{\text{2}} }\) and \(a_{{\text{Al}}_{\text{2}} {\text{O}}_{\text{3}} }\) of the magma and by the nature of the ion providing charge balance in the octahedral site. Of these \(a_{{\text{SiO}}_{\text{2}} }\) is dominant and variations in the Al3+ content of the Jimberlana pyroxenes correspond closely with the expected changes in the \(a_{{\text{SiO}}_{\text{2}} }\) of the melt. The substitution of divalent ions, such as Mn2+ and Ni2+, in the pyroxene lattice is by replacement of Fe2+ or Mg2+ in the octahedral M 3 and M 2 sites and is therefore independent of charge balance. If there are no size restrictions, the principal factor to be considered is the CFSE the ion receives in octahedral co-ordination. Ni2+, which receives a high CFSE, partitions strongly between the early-formed pyroxenes and olivines and therefore becomes depleted in the magma with fractionation. Conversely Mn2+, which receives zero CFSE, concentrates in the magma with fractionation and becomes a more important substitute in the later-formed pyroxenes. Its geochemical behaviour is controlled by its size. The narrow miscibility gap of the Jimberlana pyroxenes and the high En content of the Ca-poor pyroxenes at the bronzite pigeonite changeover suggest that these pyroxenes crystallised at a higher temperature than pyroxenes of comparable composition from other intrusions. 相似文献