内蒙古中西部宝音图群石榴角闪岩的地球化学、变质作用及年代学特征

宝音图群分布于内蒙古中西部狼山、图古日格和达茂旗一带，主要由云母片岩、石英片岩、石英岩、角闪岩和大理岩组成。在狼山格尔敖包沟和图古日格西南地区发育十分典型的石榴角闪岩，均以似层状或透镜状产自云母片岩中，但两地具有不同的矿物组合，前者主要以石榴石+角闪石+斜长石+含钛矿物（金红石和钛铁矿）为特征，后者主要以石榴石+角闪石+绿帘石+含钛矿物（金红石和钛铁矿）为特征。地球化学研究显示两个地区的石榴角闪岩原岩具有相似的化学组成，均为亚碱性玄武岩的拉斑系列。宝音图群的石榴角闪岩具有右倾的稀土配分模式，REE总量为83.31×10^-6~125.9×10^-6，（La/Yb）_N比值为2.17~6.48，δEu=0.87~0.98。Ta、Nb、Ti没有明显的负异常，其配分型式类似E-MORB特点。微量元素构造判别图解表明这些石榴角闪岩的原岩产于板内拉张环境中。本文通过模拟格尔敖包沟样品LS01和图古日格西南地区样品LS35的P-T视剖面图研究其变质作用及矿物演化过程，结果显示这两个样品均经历了早期进变质，峰期以及峰后近等温减压的顺时针型P-T轨迹。样品LS01的峰期温压条件为~11kbar/~735℃，模拟得到的峰期矿物组合可能为石榴石+角闪石+斜长石+黑云母+透辉石+金红石+熔体，P-M（H₂O）视剖面图显示，由于峰后演化过程中存在饱和流体渗透，导致峰期透辉石无法保留。样品LS35的峰期温度压力条件为~8kbar/675℃，其峰期组合为石榴石+角闪石+绿帘石+金红石。两个地区的石榴角闪岩的温度压力条件明显不同，推测宝音图群中呈透镜体或似层状产出的变质基性岩，存在着递增型的变质作用。锆石LA-ICP-MS U-Pb年代学的研究结果显示石榴角闪岩样品LS01的变质锆石年龄为394±8Ma。由此推测这些石榴角闪岩的原岩可能形成于华北北缘在新元古代发育的裂陷盆地，在泥盆纪中期，宝音图群作为华北克拉通的一部分，被卷入到与古亚洲洋闭合有关的造山过程，发育中压型递增变质作用。     

麻粒岩相变质作用与花岗岩成因-I:变质泥质岩/杂砂岩高温-超高温变质相平衡

麻粒岩相岩石作为洞察下地壳的窗口一直备受重视。二十世纪九十年代以来麻粒岩研究的一个重要进展是利用变质相平衡的定量研究方法模拟岩石中所发生的深熔变质反应、熔体成分变化、及熔体丢失对变质矿物组合的影响等。本文利用KASH、NKASH和KFMASH等简单体系的相平衡关系,做出P-T投影图、组分共生图解和基于固定全岩成分的P-T视剖面图解,并结合有关实验岩石学结果,讨论了高温和超高温条件下变质泥质岩和杂砂岩中的变质熔融反应、矿物组合、全岩成分与P-T条件之间的相互关系。多数变质泥质岩和杂砂岩中饱和流体固相线熔融反应可利用NKASH体系中有水流体参与的熔融反应模拟,在没有外来流体注入时,这些反应可形成<3mol%熔体。在不同体系中白云母脱水熔融反应型式及其P-T条件不同,如在NKASH和KFMASH体系中模拟计算的白云母脱水熔融反应与相应的实验结果相似,分别控制了白云母分解熔融的温度下限和上限;白云母的分解温度会随着其中Fe、Mg和Ti含量的增加而升高,也随着共生斜长石中钙长石组分增加而升高,泥质岩中白云母脱水熔融可以形成~10mol%熔体。在KFMASH体系中黑云母脱水熔融反应表现为4条单变反应,其理论计算的温度比实验模拟的结果低一些。在NCKFMASH体系或实际岩石中黑云母脱水熔融反应为滑动反应,如NCKFMASH体系中黑云母从其开始熔融到最后消失在泥质岩中可跨越~100℃,在杂砂岩中可跨越30~50℃。黑云母的稳定温度随着镁值升高而升高,其稳定上限受钛影响更大,黑云母脱水熔融可以形成超过30mol%~40mol%熔体。KFMASH体系中的相平衡模拟表明以出现斜方辉石+夕线石和假蓝宝石为特征的超高温组合易于出现于富镁泥质岩中,而对正常成分泥质岩在达到1000℃的超高温条件下,主要出现石榴石+夕线石(即夕线榴),该组合在更高温度反应形成假蓝宝石+尖晶石。利用饱和水固相线反应和白云母与黑云母分解反应可以更好地限定不同的变质相。如中压和低压条件下低角闪岩相和高角闪岩相的界限可利用NKASH体系中有水流体和白云母参与的熔融反应和亚固相线条件下的白云母分解反应限定;实验确定的泥质岩中黑云母开始熔融与消失的反应可分别用于限定高角闪岩相与(正常)麻粒岩相的界限,以及(正常)麻粒岩相和超高温麻粒岩相的界限。因此,从矿物组合角度,正常麻粒岩相可限定在黑云母开始熔融到完全消失的温度范围,超高温麻粒岩相可限定在黑云母消失(有石英存在)之后的温度范围。     

柴西缘花土沟超高温变质地体中的镁铝麻粒岩岩石成因及其与熔体行为的关系

镁铝麻粒岩泛指一类全岩化学成分富镁、铝的麻粒岩相变质岩,是研究超高温变质作用的峰期变质条件和变质演化历史的重要对象,但目前对它的原岩属性和岩石成因的认识仍十分有限。本文以柴达木地块西缘的花土沟超高温变质地体为例,在野外调查基础上,对镁铝麻粒岩和泥质片麻岩进行了岩相学和全岩地球化学分析,发现镁铝麻粒岩与含浅色体的泥质片麻岩的SiO₂、TiO₂、P₂O₅ 含量相似,^TFe₂O₃、Al₂O₃、MnO、CaO、Na₂O含量虽有差异但变化范围存在交集。此外,两类岩石具有相似的微量和稀土元素配分曲线,结合两者的矿物组合也存在相似性,提出花土沟镁铝麻粒岩的原岩可能是与泥质片麻岩类似的泥质沉积岩。从低角闪岩相变泥质岩到含浅色体的泥质片麻岩,再到镁铝麻粒岩,其全岩化学成分向着贫铝、钙、钾、钠,富铁、镁的趋势变化。其中,高X_Mg值（0.51~0.69）是镁铝麻粒岩与其他泥质片麻岩（X_Mg=0.34~0.43）的最大差别。通过对变泥质岩的相平衡模拟和理论计算,发现部分熔融和熔体丢失能解释大部分的变化趋势,但基本不影响全岩X_Mg值;只有在进变质升温过程中丢失含石榴子石的熔体才能造成变泥质岩的镁铝麻粒岩化。此外,富石榴子石的泥质残留体相比附近的含浅色体泥质片麻岩,贫硅、钠、钾,富集铝、铁、镁、锰、钙,重稀土元素含量显著高于后者,上述地球化学特征对应石榴子石熔体的加入而后长英质熔体的丢失,支持野外观察到的熔体携带石榴子石迁移的现象。最后,对镁铝麻粒岩只呈透镜体产出的原因做出了推测,即熔体很难带着石榴子石完成长距离迁移,只有被长英质正片麻岩包围的泥质沉积物,其进变质加热阶段形成的熔体才能携带石榴子石完全迁出原岩,促成变泥质岩透镜体的镁铝麻粒岩化,目前仍需更多的相关研究来验证这一推测。在世界其他高温-超高温变质岩区,石榴子石熔体的迁出和泥质岩的镁铝麻粒岩化可能也不同程度有所保留和记录。     

西大别造山带红安高压榴辉岩的变质演化：岩相学与Na2O-CaO-K2O-FeO-MgO-Al2O3-SiO2-H2O-O(Fe 2O3)体系中相平衡关系

西大别造山带红安高压榴辉岩主要矿物为石榴石、绿辉石、冻蓝闪石、石英和绿帘石,有时可见蓝闪石、多硅白云母和钠云母。石榴石具有生长环带且边缘成分变化大,可分为代表峰期的Ⅰ型边（X_Mg高、Grs低）和受退变质改造的Ⅱ型边（X_Mg低、Grs高）。石榴石内蓝闪石包体发育冻蓝闪石退变边,说明包体不能完全反映进变质条件。基质绿辉石比包体绿辉石Jd含量低,在一个晶体内成分有明显变化和沿解理缝发育冻蓝闪石,显示峰后绿辉石有成分变化和退变质改造。基质中冻蓝闪石晶体较大,核部见有蓝闪石残留,说明二者有成因联系。冻蓝闪石和绿辉石都发育后成合晶结构,石榴石有韭闪石的反应冠状体。在THERMOCALC程序计算的P-T视剖面图中,石榴石Ⅰ型边反映的峰期P-T条件为2.4~2.6GPa、570~585℃,和基质中多硅白云母Si含量等值线限定范围一致,对应硬柱石蓝闪石榴辉岩组合。石榴石Ⅱ型边P-T范围为1.9~2.4GPa、530~570℃,低于峰期条件。在可能的峰后降压过程中,岩石先后主要经历了硬柱石脱水生成绿帘石和蓝闪石、绿辉石退变为冻蓝闪石的反应阶段。绿辉石、冻蓝闪石发育的后成合晶说明晚期退变过程缺乏流体,石榴石的韭闪石冠状体也可能在该阶段产生,都受局部成分域控制。红安高压榴辉岩中各矿物与成分代表不同变质阶段,称其为冻蓝闪石榴辉岩只是对现有主要组成矿物的描述,不是基于共生关系的严格岩石学命名。     

西大别熊店地区榴辉岩变质作用的P-T轨迹研究

西大别熊店地区的榴辉岩多属于高压榴辉岩,主要矿物为石榴石、角闪石、绿辉石、绿泥石、白云母、石英、以及少量金红石及长石。石榴石具有明显的生长环带。本次研究利用榴辉岩样品的全岩成分定量的绘制了P-T视剖面图,根据石榴石的端元成分含量,计算得出了石榴石成分剖面所对应的温压条件。其核部的温压条件为21. 5 × 10 ⁸ Pa ～ 22. 2 × 10 ⁸ Pa,450℃ ～ 463℃,对应的矿物组合为石榴石 + 绿辉石 + 蓝闪石 + 阳起石 + 硬柱石 + 绿泥石 + （白云母 + 水）;边缘的温压条件为6 × 10 ⁸ Pa ～ 8 × 10 ⁸ Pa,610℃ ～ 630℃,该温压条件对应的矿物组合为石榴石 + 普通角闪石 + 斜长石 + 透辉石 ＋ （白云母 + 水）,从而得到石榴石变质演化的P-T轨迹,由此反映出石榴石变质过程是一个升温降压的过程。     

赞皇前寒武纪变质杂岩区变质反应结构与变质作用P-T-t轨迹

赞皇变质杂岩位于华北克拉通中部造山带中南段、太行山东麓低山区。出露于该变质杂岩区中南部的含石榴石的斜长角闪片麻岩、泥质片麻岩,均保存了三期矿物组合:进变质、峰期变质和退变质矿物组合。这两大类变质岩石中,进变质阶段矿物组合(M₁)以石榴石变斑晶核部的包裹体矿物组合为代表,变质高峰期矿物组合(M₂)由石榴石变斑晶"边部"和基质矿物组成,退变质阶段矿物组合(M₃)主要是环绕石榴石边部发育的"白眼圈"状后成合晶矿物组合。泥质片麻岩中的石榴石变斑晶均保存了明显的成分环带,且在边部很窄的范围内X_Mn有所增加、Mg/(Mg+Fe)有所降低,指示存在变质高峰期后的退变质过程。温度与压力计算结果表明,赞皇斜长角闪片麻岩所经历的进变质阶段(M₁)温度约为640~710℃、 压力约为8.2~8.6kbar;高峰期(M₂)变质温度超过810℃,压力大于12.1kbar;退变质阶段(M₃)的温压范围为590~670℃和3.2~5.6kbar。此前的研究已说明泥质片麻岩的进变质阶段(M₁)变质温度为660~690℃,压力为9.0~9.2kbar;高峰期(M₂)变质温度超过780℃,压力大于12.5kbar。变质高峰属于中压相系的顶部至高压相系的底部。斜长角闪片麻岩、泥质片麻岩均记录了典型的顺时针P-T轨迹,并显示近等温减压(ITD)的退变质片段。对泥质片麻岩中多颗锆石的变质增生边的SHRIMP U-Pb定年表明,变质高峰期时代为1821±17Ma。变质作用历史说明赞皇变质岩区卷入了华北克拉通东部陆块和西部陆块之间的俯冲-碰撞、随后的快速隆升过程,为华北克拉通中部造山带早元古代末期(~1850Ma)存在的造山事件提供了新的证据 。     

视剖面图温压计研究进展评述

视剖面图温压计是目前定量估算变质温度和压力的主要方法之一。其理论基础为热力学平衡原理与质量守恒定律。利用内恰的热力学数据库和相应的成分-活度模型对特定成分体系进行视剖面图计算,可以正演模拟给定温度和压力条件下的矿物组合、矿物丰度及其成分,与实测岩石对比,可以准确获取岩石的形成温度和压力。在应用视剖面图温压计时,应选择受全岩成分影响小、且受退变质作用影响微弱的矿物成分;对于有成分变化的体系,应结合多种方法恢复有效全岩成分。文中通过视剖面图对KFMASH(K2O-Fe O-Mg O-Al2O3-Si O2-H2O)体系下不同矿物组合内多硅白云母硅含量及其等值线斜率的研究,认为多硅白云母硅含量及其等值线斜率主要由不同矿物组合内多硅白云母参与的契尔马克替换及纯转换端元反应中的主导反应决定,进一步深化了对变质过程中控制矿物成分变化的内部缓冲反应机制的理解,从而也可为选择和应用矿物温压计提供指导。因此,视剖面图方法是目前研究变质岩石形成条件及变质作用精细过程的最佳方法之一。     

麻粒岩的研究进展与方法

近年来,有关麻粒岩的研究取得了长足进展,本文讨论了4个相关问题:(1)麻粒岩的大地构造环境与P-T轨迹。麻粒岩可以形成于4种大地构造环境中:(a)碰撞造山带以形成高压麻粒岩为特征,为中压相系,包括曾位于地壳浅部的岩石经历构造埋深达到变质峰期后再折返的过程,为顺时针型P-T轨迹;也包括曾经历洋壳或陆壳俯冲形成的高压-超高压榴辉岩相岩石折返叠加变质形成的麻粒岩,P-T轨迹以减压为主。(b)地壳伸展区以形成低压麻粒岩为特征,并可达到超高温条件,其P-T轨迹为减压加热至温度峰期,随后发生等压或降压冷却。(c)岛弧或陆缘岩浆增生区的下地壳多为高压麻粒岩相,其中侵入的辉长岩首先经历等压冷却,然后再经历升温升压进变质过程。(d)太古宙克拉通麻粒岩相表壳岩呈皮筏状分布于TTG片麻岩内部,多达到超高温条件,发育逆时针型P-T轨迹,受太古宙特殊的垂直构造体制控制。(2)麻粒岩的进变质过程与流体行为。按照流体行为,麻粒岩的进变质过程分为3种型式:(a)流体饱和进变质过程,指岩石在饱水固相线之前达到流体饱和,随后发生饱水固相线熔融与含水矿物的脱水熔融,以及阶段性熔体丢失,导致岩石中水含量降低,缺流体固相线温度升高;在峰期之后的降温过程中,发生熔融反应的逆反应,或结晶反应,形成含水矿物,结晶反应终止于缺流体固相线。(b)流体不饱和或缺流体进变质过程,指岩石在进变质过程中会处于流体缺失状态,不会发生变质反应,岩石中原来的矿物组合以亚稳定状态保留至缺流体固相线后,才开始变质演化,因此经常形成一些不平衡结构。(c)流体过饱和进变质过程,指有过量水参与的熔融反应过程,也称为水化熔融,与熔体注入或局部汇聚有关;水化熔融过程中会更多地消耗斜长石、石英及辉石等无水矿物,导致残余物中富集角闪石和黑云母等含水矿物。(3)确定麻粒岩P-T条件的视剖面图方法。利用视剖面图方法分析麻粒岩的变质条件时,首先需要通过岩相学观察区分出峰期组合和最终组合;然后通过计算T-M(H2O)图解确定最终组合的含水量;最后利用所确定的水含量计算P-T视剖面图。利用P-T视剖面图分析麻粒岩的峰期变质条件时,首先找到峰期矿物组合在视剖面图上的稳定域,然后再结合有价值的矿物成分等值线确定P-T条件。特别需要注意的是,岩相学观察确定的峰期组合和最终组合都可能受局部结构域控制,与滞留熔体的不均匀分布或原地分凝有关,此时不能简单地用全岩成分模拟其相平衡关系。(4)相平衡模拟时需要选择有效的全岩成分。当选择实测全岩成分进行相平衡模拟时,首先需要检验其有效性,即检验实测全岩成分是否能够代表薄片中所观察到的相平衡关系。方法是计算有效全岩成分,并与实测全岩成分进行对比。对于成分不均匀的变质岩石,需要处理局部结构域的成分。分如下3种情况:(a)宏观尺度的结构域,可以分别取样;(b)微观尺度的结构域,需要在显微薄片中进行图像分析,针对不同结构域分别进行相平衡模拟;(c)由叠加或退变质形成的结构域,需要确定相应的变质反应,通过对反应配平,确定有效全岩成分。此外,文中还介绍了计算岩石中的水含量、O含量和各种矿物相含量的方法与注意事项。     

新疆西南天山哈布腾苏河高压-超高压变质带中榴辉岩和蓝片岩的岩石学及变质演化

对西南天山哈布腾苏河一带出露的典型榴辉岩和蓝片岩进行了详细的岩相学、矿物化学和温压条件综合研究。榴辉岩可分为蓝闪石榴辉岩、钠云母榴辉岩、绿帘石榴辉岩和蓝闪石榴角闪岩（退变榴辉岩）4类,蓝片岩可分为含蓝闪石石榴白云母钠长片岩、石榴白云母蓝闪片岩和石榴白云母蓝闪石英片岩3类。新鲜榴辉岩主要矿物组合为石榴石+绿辉石+钠云母+绿帘石,退变榴辉岩则为石榴石+蓝闪石+角闪石;蓝片岩主要矿物组合为石榴石+蓝闪石+多硅白云母+钠云母+钠长石+石英。榴辉岩和蓝片岩中石榴石变斑晶均保存进变质生长环带,从核部到边部X_Mn和X_Fe降低,X_Mg和X_Ca升高,指示了升温进变质的演化过程。根据榴辉岩矿物共生组合、石榴石内部包体组合分布特征及传统地质温压计估算结果,确定榴辉岩经历了4阶段的变质演化：早期硬柱石蓝片岩相进变质阶段、峰期榴辉岩相变质阶段（t=543～579℃,p=1.5～1.6 GPa）、峰后绿帘蓝片岩相退变质阶段（t=～450℃,p<1.0 GPa）和晚期蓝闪绿片岩相退变质阶段（t<400℃,p<0.5 GPa）。利用p-T视剖面图计算的榴辉岩、蓝片岩峰期变质温压条件与传统地质温压计估算结果十分相近,其中榴辉岩的峰期变质条件t=520～550℃,p=1.7～1.9 GPa;蓝片岩峰期变质条件t=520～620℃,p=1.7～2.3 GPa。本文估算的榴辉岩峰期变质压力条件与前人根据柯石英的发现而认为研究区部分榴辉岩及其围岩曾经历超高压变质作用的认识明显相悖,原因可能如下：① 后期退变质作用引起研究区榴辉岩全岩成分、矿物化学成分的调整,在采用Grt-Cpx-Phe温压计和以全岩成分为基础的相平衡模拟方法估算峰期温压条件时受到影响,从而使估算峰期压力条件普遍偏低;② 西南天山的榴辉岩可能并非全都经历了超高压变质作用,高压、超高压榴辉岩可能分别代表了不同变基性岩块在不同俯冲深度变质的产物。     

新疆图拉尔根镁铁-超镁铁质杂岩体镍铜钴成矿岩浆作用过程:流体化学与碳同位素组成制约

东天山造山带的图拉尔根镁铁-超镁铁杂岩体为一个早古生代长期活动的幔源岩浆通道,大型铜镍钴硫化物矿体赋存于Ⅰ号超镁铁质岩体的顶部,不同类型岩石中辉石矿物的流体挥发份化学组成以H₂O为主（平均91%,5400.4mm³/g）,其次为H₂（2.0%）、H₂S（2.3%）和CO₂（2.1%）;赋矿角闪橄榄岩中CO₂和H₂S含量最高,辉长岩中流体挥发份含量低于辉石橄榄岩和橄榄辉石岩等岩浆早期结晶的岩石。CO₂和CH₄的δ¹³C值位于地壳与甲烷氧化的范围内,甲烷同系物的碳同位素组成具有正序分布模式,部分样品（TLG512）释出的CH₄和C₂H₆具有较重的δ¹³C值和反序分布特征。表明I号岩体不同类型岩石可能是不同期次岩浆活动的产物,成矿岩浆具有富H₂O和H₂S的特征,可能起源于被流体交代的亏损地幔源区,混染壳源组分可能为俯冲板片来源蚀变沉积有机质组分。     

Long length scales of element transport during reaction texture development in orthoamphibole-cordierite gneiss: Thor-Odin dome,British Columbia,Canada

First-order factors controlling the textural and chemical evolution of metamorphic rocks are bulk composition and pressure–temperature–time (P–T–t) path. Although it is common to assume that major element bulk composition does not change during regional metamorphism, rocks with reaction textures such as corona structures record evidence for major changes in effective bulk composition (EBC) and therefore provide significant insight into the scale, pathways, and mechanisms of element transport during metamorphism. Quantifying changes in EBC is essential for petrologic applications such as calculation of phase diagrams (pseudosections). The progressive growth of complex corona structures on garnet and Al₂SiO₅ porphyroblasts in orthoamphibole-cordierite gneiss Thor-Odin dome (British Columbia, Canada) reduced the EBC volume of the rock during metamorphism and therefore had a dramatic effect on the evolution of the stable mineral assemblage. These rocks contain a chemical and textural record of metamorphic reactions and preserve 3D networks (reaction pathways) connecting corona structures. These coronal networks record long (>cm) length scales of localized element transport during metamorphism. P–T, T–X, and P–X pseudosections are used to investigate the control of effective bulk composition on phase assemblage evolution. Despite textural complexity and evidence for disequilibrium, mineral assemblages and compositions were successfully modeled and peak metamorphic conditions estimated at 750°C and 9 kbar. These results illustrate how textural and chemical changes during metamorphism can be evaluated using an integrated petrographic and pseudosection approach, highlight the importance of effective bulk composition choice for application of phase equilibria methods in metamorphic rocks, and show how corona structures can be used to understand the scale of compositional change and element transport during metamorphism.     

Fractionation of bulk rock composition due to porphyroblast growth: effects on eclogite facies mineral equilibria, Pam Peninsula, New Caledonia

Chemically zoned porphyroblasts in metamorphic rocks indicate that diffusional processes could not maintain equilibrium conditions on a grain scale during porphyroblast growth or establish it afterwards. An effect of this inability to maintain equilibrium is the progressive removal of elements forming garnet cores from any metamorphic reaction that occurs at the porphyroblast boundaries or in the matrix of the rock. To examine this effect on mineral assemblages, the Bence–Albee matrix correction was applied to X‐ray intensity maps collected using eclogite samples from northern New Caledonia in order to determine the chemical composition of all parts of the sample. The manipulation of these element maps allows a quantitative analysis of the fractionation of the bulk rock composition between garnet cores and the matrix. A series of calculated equilibrium‐volume compositions represents the change in matrix chemistry with progressive elemental fractionation as a consequence of prograde garnet growth under high‐P conditions. Pressure–temperature pseudosections are calculated for these compositions, in the CaO–Na₂O–FeO–MgO–Al₂O₃–SiO₂–H₂O system. Assemblages, modal proportions and mineral textures observed in the New Caledonian eclogites can be closely modelled by progressively ‘removing’ elements forming garnet cores from the bulk rock composition. The pseudosections demonstrate how chemical fractionation effects the peak metamorphic assemblage, prograde textures and the development of retrograde assemblages.     

Phase equilibria modelling of kyanite‐bearing anatectic paragneisses from the central Grenville Province

Kyanite‐bearing paragneisses from the Manicouagan Imbricate Zone and its footwall (high‐P belt of the central Grenville Province) preserve evidence of partial melting with development of metamorphic textures involving biotite–garnet ± kyanite ± plagioclase ± K‐feldspar–quartz. Garnet in these rocks displays a variety of zoning patterns with respect to Ca. Pseudosection modelling in the Na₂O–CaO–K₂O–FeO–MgO–Al₂O₃–SiO₂–H₂O–TiO₂–O (NCKFMASHTO) system using measured bulk rock compositions accounts for the textural evolution of two aluminous and two sub‐aluminous samples from the presumed thermal peak to conditions at which retained melt solidified. The prograde features are best explained by pseudosections calculated with compositions to account for melt loss. The intersection of isopleths of grossular content and Fe/(Fe + Mg) relating to large porphyroblasts of garnet provide constraints on the P–T conditions of the metamorphic peak. These P–T estimates are considered to be minima because of the potential for diffusional modification of the composition of garnet at high‐T and during the early stages of cooling. However, they are consistent with textural observations and pseudosection topology, with peak assemblages best preserved in rocks for which the calculated pseudosections predict only small changes in mineral proportions in the P–T interval, in which retrograde reactions are inferred to have occurred between the thermal peak and the solidus. Maximum P–T conditions (14.5–15.5 kbar and 840–890 °C) and steep retrograde P–T paths inferred for rocks from the Manicouagan Imbricate Zone are comparable with those determined for mafic rocks from the same area. In contrast, maximum P–T conditions of 12.5–13 kbar and 815–830 °C and flatter P–T paths are inferred for the rocks of the footwall to the Manicouagan Imbricate Zone. The general consistency between textures, mineral compositions and the topologies of the calculated pseudosections suggests that the pseudosection approach is an appropriate tool for inferring the P–T evolution of high‐P anatectic quartzo‐feldspathic rocks.     

高压-超高压变质岩石中石榴石的环带和成因

在俯冲带变质过程中,石榴石是高压-超高压变质榴辉岩和片麻岩的常见变质矿物。由于石榴石具有难熔和流体中的低溶解能力的特点,通常可以很好地保存下来,并且能够保留复杂的化学成分环带,以及不同类型的矿物或流体包裹体,为解释石榴石寄主岩石经历的变质演化历史提供了重要信息。石榴子石的主微量元素成分受控于很多因素,如全岩成分、变质的温压条件、控制石榴子石形成的相关变质反应、与石榴子石共生的矿物种类和成分等。因此,在利用石榴石探讨超高压变质的演化历史时,对石榴石进行系统的主要元素、微量元素、氧同位素以及矿物包裹体分析,以及相互间的成因关系。同时,对石榴石中的锆石或独居石包裹体并进行原位U-Pb定年和微量元素分析,可以为变质石榴石的形成时代提供直接的时间制约。深入研究超高压变质岩中石榴石的生长阶段,不仅可以为含石榴石寄主岩石的变质过程提供岩石学和地球化学证据,而且对于理解石榴石的形成机制、生长规律及其变质化学动力学过程具有重要的科学意义。     

Pumpellyites and coexisting minerals in different low-grade metamorphic facies of Liguria, Italy

Pumpellyite from four-phase assemblages (pumpellyite + epidote + prehnite + chlorite; pumpellyite + epidote + actinolite + chlorite; pumpellyite + epidote + Na-amphibole + chlorite, together with common excess phases), considered to be low variance in a CaO-(MgO + FeO)-Al₂O₃-Fe₂O₃ (+Na₂O + SiO₂+ H₂O) system, have been examined in areas which underwent metamorphism in the prehnite-pumpellyite, pumpellyite-actinolite and low-temperature blueschist facies respectively. The analysed mineral assemblages are compared for nearly constant (basaltic) chemical composition at varying metamorphic grade and for varying chemical composition (basic, intermediate, acidic) at constant metamorphic conditions (low-temperature blueschist facies). In the studied mineral assemblages, coexisting phases approached near chemical equilibrium. At constant (basaltic) bulk rock composition the MgO content of pumpellyite increases, and the X_Fe3+ of both pumpellyite and epidote decreases with increasing metamorphic grade, the Fe³⁺ being preferentially concentrated in epidote. Both pumpellyite and epidote compositions vary with the bulk rock composition at isofacial conditions; pumpellyite becomes progressively enriched in Fe and depleted in Mg from basic to intermediate and acidic bulk rock compositions. The compositional comparison of pumpellyites from high-variance (1–3 phases) assemblages in various bulk rock compositions (basic, intermediate, acidic rocks, greywackes, gabbros) shows that the compositional fields of both pumpellyite and epidote are wide and variable, broadly overlapping the compositional effects observed at varying metamorphic grade in low-variance assemblages. The intrinsic stability of both Fe- and Al-rich pumpellyites extends across the complete range of the considered metamorphic conditions. Element partitioning between coexisting phases is the main control on the mineral composition at different P-T conditions.     

Controls of mineral reactions in high-grade garnet–wollastonite–scapolite-bearing calcsilicate rocks: an example from Anakapalle, Eastern Ghats, India

ABSTRACT A suite of garnet-wollastonite-scapolite-bearing calcsilicate granulites from the Eastern Ghats has been investigated to document the controls of mineral reactions during the metamorphic evolution of the deep continental crust. The rocks studied show heterogeneity in modal mineralogy and phase compositions in millimetre-sized domains. Textural relations, and the compositional plots of the phases, established that the clinopyroxene exerts a strong influence on the formation and composition of garnet in the complex natural system. P-T estimates using the vapour-independent equilibria involving garnet define a near isobaric cooling path from c. 850C at c. 5.5–5.2 kbar. The deduced trajectory tallies well with the terminal segment of the overall retrograde P-T path construed from the associated rocks using well-calibrated thermobarometers. The ubiquitous occurrence of wollastonite and scapolite in the main calcsilicate body suggests low a_CO2 during peak metamorphic condition. Fluid compositions constrained from mineral-fluid equilibria of the garnet-bearing assemblages show domainal variations as a function of the compositions of the solid phases, e.g. garnet and clinopyroxene. A quantitative log/_CO2-log/_O2 diagram has been constructed to depict the stability of the different calcsilicate assemblages as functions of the compositions and the behaviour of these fugitive species. The results of the mineral-fluid equilibria and the quantitative fluid/rock ratio calculations, in conjunction with the topological constraints, imply vapour-deficient meta-morphism in the rocks studied. It is argued that f_O2 during peak metamorphism was monitored by the ambient f_O2. Subsequently, during retrogression, different domains evolved independently, whereas the fluid composition was controlled by the mineral-fluid equilibria.     

P-T estimates and timing of the sapphirine-bearing metamorphic overprint in kyanite eclogites from Central Rhodope, northern Greece

Sapphirine-bearing symplectites that replace kyanite in eclogites from the Greek Rhodope Massif have previously been attributed to a high-pressure granulite-facies metamorphic event that overprinted the eclogitic peak metamorphic assemblage. The eclogitic mineralogy consisted of garnet, omphacitic pyroxene, rutile and kyanite and is largely replaced by low-pressure minerals. Omphacite was initially replaced by symplectites of diopside and plagioclase that were subsequently replaced by symplectites of amphibole and plagioclase. Garnet reacted during decompression to form a corona of plagioclase, amphibole and magnetite. Rutile was partly transformed to ilmenite and kyanite decomposed to produce a high-variance mineral assemblage of symplectitic spinel, sapphirine, plagioclase and corundum. The presence of quartz and corundum in the kyanite eclogites is evidence for the absence of bulk equilibrium and obviates a conventional analysis of phase equilibria based on the bulk-rock composition. To circumvent this difficulty we systematically explored the pressure-temperature-composition (P-T-X) space of a thermodynamic model for the symplectites in order to establish the pressure-temperature (P-T) conditions at which the symplectites were formed after kyanite. This analysis combined with conventional thermometry indicates that the symplectites were formed at amphibolite-facies conditions. The resulting upper-pressure limit (～0.7 GPa) of the sapphirine-producing metamorphic overprint is roughly half the former estimate for the lower pressure limit of the symplectite forming metamorphic event. Temperature was constrained (T ～ 720°C) using garnet-amphibole mineral thermometry. The P-T conditions inferred here are consistent with thermobarometry from other lithologies in the Rhodope Massif, which show no evidence of granulite-facies metamorphism. Regional geological arguments and ion-probe (SHRIMP) zircon dating place the post-eclogite-facies metamorphic evolution in Eocene times.     

Phase relationships in Buchan facies series pelitic assemblages: calculations with application to andalusite-staurolite parageneses in the Mount Lofty Ranges,South Australia

Low-pressure, medium- to high-temperature (Buchan-type) regional metamorphism of pelitic rocks in the Mount Lofty Ranges, South Australia, is defined by the development of biotite, staurolite-andalusite, fibrolite, prismatic sillimanite and migmatite zones. K-feldspar makes its first appearance in the prismatic sillimanite zone and here we restrict our discussion to lower grade assemblages containing prograde muscovite, concentrating particularly on well-developed andalusitestaurolite parageneses. In general, the spatial distribution and mineral chemical variation of these assemblages accord with the predictions of petrogenetic grids and P-T and T-X _Fe pseudo-sections constructed from the internally consistent data set of Holland and Powell (1990) in the system KFMASH, assuming a(H₂O) 1, although analysed white mica compositions are systematically more aluminous than predicted. Importantly, the stability ranges of most critical assemblages predicted by these grids and pseudo-sections coincide closely with P-T estimates calculated using the data set of Holland and Powell (1990) from the Mount Lofty Ranges assemblages. With the exception of Mn in garnet and Zn in one staurolite-cordierite-muscovite assemblage non-KFMASH components do not significantly appear to have affected the stability ranges of the observed assemblages. An apparent local reversal in isograd zonation in which andalusite first appears down-grade of staurolite suggests a metamorphic field gradient concave towards the temperature axis and, together with evidence for essentially isobaric heating of individual rocks, is consistent with the exposures representing an oblique profile through a terrain in which heat was dissipated from intrusive bodies at discrete structural levels.Mineral abbreviations used in figures als Al₂SiO₅ phase - bi biotite - chl chlorite - ky kyanite - ph phengite - sill sillimanite - and andalusite - cd cordieritc - gt garnet - mu muscovite - q quartz - st staurolite