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本文讨论了熔体中矿物的热流控制生长。作者按照传导方程的自由边界问题,在地质条件容许的范围内,导出了计算矿物生长速度和生长大小的公式,并以已有实验数据对计算公式进行了验证,还得到了计算透辉石-钙铝辉石固溶体生长速度和生长大小所需的导热系数。讨论认为本文模型适用于自然界在较高温度下从单组份熔体中缓慢结晶的矿物。 相似文献
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接触交代夕卡岩型矿床中石榴子石和辉石成分特点及其与矿化的关系 总被引：1，自引：0，他引：1
本文对中国十四个接触交代钙夕卡岩矿床和钙-镁夕卡岩矿床中的三百多个样品的石榴子石和辉石成分进行了电子探针分析。不同矿床类型的石榴子石和辉石成分代表着钙夕卡岩矿床的十个矿种(Fe、Fe-Cu、Pb-Zn、W、Sn、Sn-Mo-Bi-W、、W-Bi-Cu-Mo、Cu-Zn、Cu-Sn、W-Zn-Cu)和钙-镁夕卡岩矿床的三个矿种(Fe-Cu、Mo、Pb-Zn)。石榴子石和辉石成分变化范围大,大多数石榴子石是含锰铝榴石+铁铝榴石+镁铝榴石小于15％(摩尔百分数)的钙铝榴石-钙铁榴石固溶体;大多数辉石是含小于5％的锰钙辉石的透辉石-钙铁辉石固溶体。有些Pb-Zn钙-镁夕卡岩矿床中的辉石显示出Mn含量有所增加。只有Sn和W钙夕卡岩矿床及Pb-Zn钙-镁夕卡岩矿床含(Sps+Alm+Pyr)总量大于15％的石榴子石。石榴子石和辉石成分与夕卡岩矿床金属矿化类型之间有某些联系。 相似文献
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自然界中矿物多以固溶体形式存在,据其晶体化学特征计算热力学性质是开展矿物成因理论研究的基础。本文引入描述二元矿物固溶体热力学性质的假三元模型,计算得到了透辉石-硬玉固溶体系列的热力学性质。该模型通过构造一种高度有序的中间相,同时考虑长程和短程有序效应,基于热力学平衡态矿物固溶体自由能最低的规律,可以计算特定组分下矿物的平衡自由能、焓和熵等热力学参数。本文针对透辉石-硬玉固溶体体系,取绿辉石为其中间有序态,计算了其活度-成分关系和温度-组分相图等,发现绿辉石随温度升高的有序无序相变为一级相变,相变温度为1 148±25 K,与实验研究结果一致。本文获得的透辉石-绿辉石-硬玉体系的热力学参数可用于视剖面图方法研究MORB成分的岩石的榴辉岩相变质作用过程。 相似文献
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变质作用温度与压力极限值的估算方法 总被引：3，自引：2，他引：1
变质矿物共生组合中缺少某种矿物,或者变质矿物的原始成分被不同程度地破坏,无法直接应用压力计或温度计算出具体的温度或压力数值时,可以根据实际情况,估算P-T的极限值.估算方法包括如下几类:(1)根据纯相矿物的相变条件,可以确定温度或压力的极限值.例如,根据Al2SiO5矿物相图可知,与红柱石平衡的矿物组合,稳定存在的压力不超过Al2SiO5矿物三相点的压力条件(0.375±0.025GPa);与夕线石平衡的矿物组合,稳定存在的温度不低于Al2SiO5矿物三相点的温度条件(504±20℃);(2)某些特殊矿物组合,其稳定域本身就具有温度或压力极限值的指示意义.例如,高温或超高温变质岩中的紫苏辉石+夕线石+石英组合,稳定存在的压力不低于1.05 GPa;假蓝宝石+石英组合稳定存在的温度不低于1050℃;(3)特殊矿物消失的反应线,可以限定温度极大值.例如,白云母脱水分解的反应,在中等压力条件下,不超过650℃,即与白云母+石英平衡共生的矿物组合一般不会高于650℃;(4)对于矿物固溶体发生出溶的情况,根据新生出溶页片和残留基体矿物,采用溶线温度计(二长石温度计、二辉石温度计、方解石-白云石温度计)计算出的温度数值,代表原先成分均匀的矿物固溶体出溶之前的温度极小值;(5)如果岩石中发生了退变质反应,要恢复变质作用高峰期的P-T条件,需要尽可能恢复高峰期的矿物成分,或者采用接近高峰期的矿物成分;(6)根据压力计模式反应中位于高压侧或低压侧的某种纯相矿物,可以确定压力极限值.例如,金红石位于GRAIL压力计模式反应的高压一侧.当岩石中缺少金红石时,可以人为假定岩石中存在金红石,计算出的压力为真实压力的极大值.由于压力计模式反应大多为纯转变反应,因此根据实际矿物组合和压力计模式反应,一般可以估算变质作用压力的极小值或极大值.估算变质作用P-T的极限值,方法并不限于本文所述的例子. 相似文献
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胶北南山口含榴辉石岩岩石学与锆石U-Pb定年的初步研究 总被引：3，自引：2，他引：1
胶北南山口镁铁-超镁铁质杂岩主要由含榴辉石岩和含榴基性麻粒岩所组成,且以不规则透镜体的形式赋存于太古宙英云闪长质片麻岩之中。岩相学观察、矿物相转变分析与矿物化学研究结果表明,胶北南山口含榴辉石岩不仅普遍发育近等温减压反应结构,即石榴石+富钙流体→单斜辉石+葡萄石+榍石±钠长石与石榴石+富钙流体+二氧化碳→角闪石+葡萄石±钠长石±方解石±榍石,指示其早期可能经历了高压麻粒岩相变质作用。而且,与南山口含榴基性麻粒岩类似,在晚期降温退变过程中,它们还经历了强烈的钙质交代作用,形成富钙矿物组合:富钙铝榴石的石榴石+次透辉石质单斜辉石+钙质角闪石+葡萄石+钠长石+方解石+榍石。SHRIMP锆石U-Pb定年结果表明,胶北南山口含榴辉石岩中的岩浆锆石记录了2900~2850Ma的207Pb/206Pb年龄,指示胶北地体在中太古代晚期存在一次重要的岩浆事件,而其变质锆石还记录了1950~1800Ma的207Pb/206Pb年龄,说明胶北南山口镁铁-超镁铁质杂岩曾卷入了胶北古元古代晚期地壳造山作用。结合研究区其它地质研究资料,本文推断胶北南山口镁铁-超镁铁质杂岩可能形成于古元古代,是华北克拉通胶-辽-吉带古元古代岩系的重要组成部分,并于1950~1800Ma期间,卷入了胶-辽-吉带古元古代造山作用,先后经历了高压麻粒岩相变质作用和晚期降温与钙质交代的联合退变质作用。 相似文献
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东天山黄山岩带因发育众多镁铁质-超镁铁质岩体和岩浆铜镍硫化物矿床而备受地质学者关注。四顶黑山岩体位于该岩带最东端,具有层状岩体特征;岩石类型有单辉橄榄岩、橄榄辉石岩、橄榄苏长辉长岩、橄榄辉长岩、辉石角闪岩、辉长岩、角闪辉长岩、闪长岩,主要造岩矿物为贵橄榄石、古铜辉石、透辉石、普通角闪石和斜长石,岩体分异较好,蚀变较发育。通过矿物显微结构特征观察以及计算得出:四顶黑山岩体中橄榄石最先结晶,其开始结晶温度大约在1419℃左右;古铜辉石和透辉石在橄榄石之后开始结晶,结晶温度分别在1100℃左右和900～1100℃之间,两矿物相在岩石中可以共存。岩体中橄榄岩相、苏长岩相发育,以及贵橄榄石+古铜辉石的矿物组合特征,表明岩体具有形成铜镍(铂)矿床的有利条件。 相似文献
8.
根据矿物成分及其结构演变,将大别山榴辉岩的退变质过程分为三个阶段:贫流体阶段、弱流体阶段和富流体阶段。贫流体阶段发生于榴辉岩相环境中,其主要作用是柯石英-石英和文石- 方解石等同质多象转变、石榴子石和绿辉石等的重结晶,以及绿辉石中硬玉和钠长石的固溶体出溶等。弱流体阶段发生于榴辉岩相退变质的晚期,含水矿物闪石、绿帘石和云母,以及钠长石等低压矿物大量形成之前,其标志是蓝晶石变斑晶和金红石脉的形成,以及浸染状金红石的富集成矿。富流体阶段始于低级角闪岩相退变质环境,并可能一直持续到近地表处。该阶段以出现大量含水和挥发份的矿物(如闪石、绿帘石、多硅白云母、钠云母、黑云母、磷灰石和碳酸盐等)为特征。围绕石榴子石和绿辉石的闪石次变边、闪 相似文献
9.
钙铁辉石-钠长石-石英和透辉石-钠长石-石英体系的实验数据能够计算钙铁辉石-硬玉和透辉石-硬玉固溶体中硬玉的剩余自由能,如后面所示,实验点的最好近似值是根据亚规则溶体方程获得的(JK): 相似文献
10.
雅鲁藏布江缝合带白朗县白岗尖晶石—石榴子石相二辉橄榄岩的相界反应及其意义 总被引：3，自引：0，他引：3
西藏白朗县白岗村蛇绿混杂岩中有一罕见的尖晶石石榴子石二辉橄榄岩小岩块,被松软的蛇纹岩化尖晶石二辉橄榄岩包裹其中。岩块中发育有碎基单斜辉石、斜方辉石中出溶单斜辉石、切过出溶单斜辉石的贯入单斜辉石和外来碎粒单斜辉石及钙质辉石+铬尖晶石→钙铁石榴子石相界反应。同时,在岩块和包壳岩石的橄榄石中出现针状硅镁石出溶物。计算这些矿物的温度压力表明,它们的温度压力都处于>800℃,>1.8GPa以上的地幔石榴子石域超高压环境,而且,经历过一个上升→俯冲→上升的"N"字形历程。 相似文献
11.
The compositions of more than 300 granets and pyroxenes from 14 contact-metasomatic calcic skarn deposits and calcic-magnesia
skarn skarn deposits in China have been examined using electron microprobe technique. The compositions of garnets and pyroxenes
from a wide variety of ore types represent ten major classes of calcic skarn deposits (Fe, Fe-Cu, Pb-Zn,W, Sn, Sn-Mo-Bi-W,
W-Bi-Cu-Mo, Cu-Zn and W-Zn-Cu) and three major classes of calcic-magnesia skarn deposits (Fe-Cu, Mo, Pb-Zn). Garnets and pyroxenes
show a wide range of variation in composition, but the majority of garnets are grossular-andradite solid solutions containing
less than 15 mol% (spessartine + almandine + pyrope), whereas most pyroxenes are diopside-hedenbergite solid solutions containing
less than 5 mol% johannesenile. Some pyroxenes from a Pb-Zn calcic-magnesia skarn deposit display an increase in Mn content.
Only Sn-W calcic skarn deposits and Pb-Zn calcic-magnesia skarn deposits contain garnets with more than 15 mol% (spessartine
+ almandine + pyrope). Some relationships have been established between the compositions of garnets and pyroxenes and the
metallization types of economically important metals in skarn deposits. 相似文献
12.
对柿竹园矽卡岩成因及其成矿作用的新认识 总被引：10，自引：0，他引：10
本文将报导柿竹园Ｗ，Ｓｎ，Ｍｏ，Ｂｉ矿床中矽卡岩矿物－石榴子石和辉石成分和石榴子石中熔融包裹体研究结果，对不同中段的１６块矽卡岩样品（９４％的标本采自第Ⅲ矿带）中的石榴子石和辉石进行了电子探针分析，共获得２３０个测点的数据，此外，还对上述中段大部分样品里的石榴子石和辉石进行了从边部到核心成分测定，共获得１３个样品的９７个测点数据，研究结果表明，绝大多数石榴子石属于含Ａｌｍ＋Ｓｐｓ＋Ｐｙｒ〈１３％（ 相似文献
13.
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
14.
本文研究了河北省涉县符山铁矿夕卡岩中石榴石的双折射性。该石榴石属钙铝-钙铁榴石系列,有较强的双折射性,重折率最大值约为0.009。加热可使双折射性减弱甚至消失。依形成温度,可将石榴石分为两群,重折射率相差一、两个数量级,形成温度较低者其双折射性强。在每一群中,重折率与分子式中八面体位置 Al 含量成上弯曲线关系,最强双折射大致在 And65 Gro35成分处。X 光单晶衍射照相出现异常,衍射点变成由数个点组成的拉长的线,这些点沿一定方向排列,强度和数目有变化,可能是因为结构中八面体位置上 Fe3+/Al 有序引起的。有序引起石榴石对称性降低,变为二轴晶,可以较好地解释石榴石双折射性的成因及其变化规律。本文还讨论了环带与双折射性的关系。 相似文献
15.
Implications to garnet-clinopyroxene geothermometry of non-ideal solid solution in jadeitic pyroxenes 总被引：1，自引：0，他引：1
Peter O. Koons 《Contributions to Mineralogy and Petrology》1984,88(4):340-347
Garnet-clinopyroxene geothermometry has been applied to numerous rock types from the blueschist and eclogite terrain of the Sesia zone in the Western Alps. Discrepancies in apparent temperatures of up to 600° C have been found suggesting substantial deviation from ideal behaviour of the garnet-clinopyroxene equilibria in certain assemblages. Assemblages containing jadeitic pyroxenes rather than omphacitic or diopsidic pyroxenes yield very low K
D (2.0) values and correspondingly high apparent temperatures (> 1,000° C). The garnets coexisting with high-Na pyroxenes have compositions similar to those coexisting with omphacitic pyroxenes. Departure from ideal behaviour of these garnets is likely to be minor and is accomodated in the formulation of the geothermometer. Numerous examples of coexisting garnet-clinopyroxene pairs indicate that there is no obvious relationship of K
D with jadeite content in pyroxenes with jadeite content less than 70%, but at higher values, K
D varies inversely with the jadeite content. The dependence of K
D upon the jadeite content in the high-Na pyroxenes is believed to be due to the preference of M2 sites for Fe2+ in the enstatite-jadeite substitution (Fe2+MgNa–1Al–1). This substitution is usually very limited and has no demonstrable effect upon X
Fe
Cpx
when the M1 (Fe2++Mg) content of the pyroxenes is high as in omphacitic and diopsidic pyroxenes. However, when the M1 (Fe2++Mg) content is low, as in jadeitic pyroxenes, the non-ideality of the enstatite type exchange has a marked effect on X
Fe
Cpx
and consequently on garnet-clinopyroxene calculations. 相似文献
16.
Using a literature survey of analyses of high-Ca pyroxene and co-existing silicate melt pairs and analyses of low-Ca pyroxene-silicate melt pairs, we have performed a thermodynamic analysis of pyroxene-melt equilibria. Three sets of mixing model pairs have been considered, based on two mixing models for liquid silicate solutions and two for pyroxene solid solutions. A modified version of a model developed by Bottinga and Weill (1972) for the mixing properties of silicate melts, in which the melt is considered to be composed of independent network-forming and network-modifying quasi-lattices, more successfully accounts for variations in melt composition than does a model which considers the melt to be composed of simple oxides which mix ideally. An empirical model for the mixing properties of pyroxenes, in which the M1 and M2 sites are considered to be equivalent and are combined as a hypothetical ‘M’ site, is as successful in accounting for variations in pyroxene composition at high temperatures as an ideal multisite mixing model.Using a variety of pyroxene-melt relations, and combinations of the mixing models outlined above, we have developed several pyroxene-melt and low-Ca pyroxene-high-Ca pyroxene geothermometers which have internally-consistent precisions of approximately ±20°C (1σ). One of the two-pyroxene geothermometers has been used to calculate ‘quench’ temperatures for a number of eucrites. Computed temperatures are subsolidus, and are consistent with independent geothermometers and with petrographic observations. The equations may also be used to calculate the composition of pyroxene crystallizing from a silicate melt of known composition, with or without independent knowledge of temperature. Internally consistent precisions vary, but are approximately ± 3 mol% Fs, ± 5 mol% En, and ±4 mol% Wo (all 1σ). These equations may have application in modeling the evolution of mineral compositions during differentiation of basaltic magmas, particularly terrestrial layered intrusions and the lunar magma ocean. 相似文献
17.
Bjørn O. Mysen 《Geochimica et cosmochimica acta》1978,42(6):871-885
Results of a survey of experimental data on trace element partitioning between crystals and coexisting liquid and between crystals and coexisting aqueous fluid are reported. These studies involve combinations of elements such as Cs, Rb, K, Na, Li, Ba, Sr, Ni and Sm dissolved in minerals such as feldspars, micas, feldspathoids, garnets, pyroxenes, amphibole and olivine. It is shown that the concentration ranges of these elements in minerals with solution behavior according to Henry's law appear to extend to less than 1 wt.% and often to less than 100 ppm of the element in the crystalline phase.The available data indicate that the concentration ranges of solution in minerals according to Henry's law can be positively correlated with the difference of ionic radii between trace element and the host element for which the tracer is assumed to substitute. Furthermore, studies involving crystals and coexisting aqueous fluid have been used to determine whether Henry's law or Raoult's law adequately describes the solution. Based on the assumption that the aqueous fluid solution can be considered ideal, models have been proposed stating that if the difference between the ionic radii of the tracer and the host element in the crystalline phase is less than about 10% (relative to the host element), the solution is ideal (Raoult's law). With larger differences between the ionic radii, there is an excess free energy of mixing, although Henry's law is still obeyed in the concentration ranges where crystalliquid or crystal-fluid partition coefficients are independent of element concentration. 相似文献
18.
Rune B. Larsen C. Kent Brooks Dennis K. Bird 《Contributions to Mineralogy and Petrology》1992,112(2-3):428-437
Solutions of H2O–NaCl–CH4 occur in fluid inclusions enclosed by quartz, apatite and feldspar from gabbroic pegmatitites, anorthositic structures and intercumulus minerals within the Skaergaard intrusion. The majority of the fluid inclusions resemble 10 m diameter sub-to euhedral negative crystals. A vapour phase and a liquid phase are visible at room temperature, solids are normally absent. The salinity of the fluids ranges from 17.5 to 22.8 wt.% NaCl. CH4, which comprises less than six mole percent of the solution, was detected in the vapour phase of the fluid inclusions with Raman microprobe analysis. Homogenization of the fluid inclusions occurred in the liquid phase in the majority of the fluid inclusions, though 10% of the inclusions homogenized in the gas phase. Thermodynamic consideration of the stability of feldspars + quartz, and the C–O–H system, indicates that the solutions were trapped at temperatures between 655 and 770°C, at oxygen fugacities between 1.5 and 2.0 log units below the QFM oxygen buffer. Textural evidence and the composition of the solutions suggest that the fluids coexisted with late-magmatic intercumulus melts and the melts which formed gabbroic pegmatites. These solutions are thought to have contributed to late-magmatic metasomatism of the primocryst assemblages of the Skaergaard intrusion. 相似文献
19.
The phase relations of pyroxenes, amphiboles and associated minerals in metamorphic rocks of the Franciscan Complex can be graphically depicted on a ternary diagram which has at its apices the metamorphic clinopyroxene end members, viz NaAl-NaFe3+-Ca(Fe2+, Mg). Phases are plotted by projection from a constant subassemblage of minerals. This analysis allows interpretation of the effects of pressure, temperature, bulk rock composition and fluid composition on stability of minerals within the Franciscan.Pyroxenes in meta-igneous rocks and metagraywackes have a limited compositional range and fall into two groups: the omphacites, with 50±5% diopside +hedenbergite component; and the jadeitic pyroxenes with 10±5% diopside+hedenbergite. Pyroxenes intermediate between these two groups are unstable relative to assemblages containing Na-amphibole+other minerals.Coexisting pyroxenes and amphiboles in eclogites and associated coarse blueschists comprise equilibrium assemblages, and the proportion of pyroxene to amphibole is a function of rock composition. Eclogites are stable at higher temperature than regionally developed fine-grained greenstones and blueschists in the Franciscan, and at higher pressure than amphibolites. X
H2O
fluid is not an important factor in the stability of Franciscan eclogite relative to amphibolite. 相似文献