俄罗斯白海活动带Uzkaya Salma地区含绿纤石榴辉岩的岩石学特征及其变质演化

俄罗斯白海活动带Uzkaya Salma地区榴辉岩中发现的绿纤石形成于榴辉岩化早期亚绿片岩相阶段。该绿纤石多以包体形式存在于退变榴辉岩的变斑晶石榴石矿物中,并与榍石、金红石、单斜辉石、绿泥石、绿帘石、石英等矿物伴生,极少量单颗粒绿纤石包裹在基质单斜辉石(透辉石)矿物中,呈浑圆状。绿纤石成分上属于铝绿纤石和铁绿纤石,其中以铝绿纤石为主。在详细的岩相学研究基础上,通过相平衡计算,结合矿物温压计计算结果,发现含绿纤石榴辉岩共经历了4阶段的变质演化:Ⅰ早期进变质阶段,以石榴石中的绿纤石+绿泥石+绿帘石+石英等矿物包裹体为特征,依据实验岩石学研究的矿物组合绿纤石+绿泥石+石英和铁绿纤石+绿帘石稳定域,估算该变质阶段温压条件t=160~320℃,p=0.2~0.8 GPa;Ⅱ峰期榴辉岩相阶段,矿物组合为石榴石+Di-Pl后成合晶推测的绿辉石+金红石±角闪石+石英,石榴石核部镁等值线和绿辉石硬玉分子等值线限定其峰期温压条件为t=725~740℃,p=1.4~1.5 GPa;Ⅲ高压麻粒岩相退变质阶段,矿物组合为石榴石+透辉石+角闪石+斜长石+石英,石榴石-单斜辉石温度计和后成合晶中斜长石钙等值线限定该阶段的温压条件t=725~750℃,p=1.1~1.3 GPa;Ⅳ晚期角闪岩相退变质阶段,矿物组合角闪石+斜长石±黑云母+石英,相平衡计算和角闪石-斜长石温度计限定温压条件为t=670~700℃,p=0.7~0.9 GPa。综上,确定了俄罗斯白海活动带Uzkaya Salma地区含绿纤石榴辉岩具有顺时针的p-T演化轨迹,峰期对应的地温梯度为15℃/km,俯冲进变质阶段经历了绿纤石-绿帘石相变质,由峰期榴辉岩相到退变质高压麻粒岩相具近等温降压的特征。研究表明,板块的"冷"俯冲作用在地球演化早期太古宙时期就可能出现了。     

南秦岭造山带东段的变质作用及其地质意义

南秦岭造山带分布于商丹和勉略两条缝合线之间,其东段变质地层以志留系和泥盆系为主,包括少量的震旦系和上古生界。主要岩性包括变质泥质岩、石英岩、大理岩和少量的变质基性岩及片麻岩等。根据野外分布和显微组构特征发现这些岩石至少遭受了两期变质作用:早期为递增变质作用,它以佛坪地区的高角闪岩相—麻粒岩相为中心,向外依次变为低角闪岩相(十字石—蓝晶石带)、绿帘角闪岩相(石榴石带)和绿片岩相(绿泥石和黑云母带),变质时代约为220～260 Ma。麻粒岩相以出现二辉石为特征,包括基性和中酸世麻粒岩等,野外只见于佛坪县城附近。高角闪岩相在泥质岩石中的矿物组合为夕线石-石榴石-黑云母-斜长石-钾长石-石英,其变质条件为t=688～693℃,P=0.5～0.6 GPa;低角闪岩相在泥质岩石中的矿物组合为蓝晶石(十字石)-石榴石-黑云母-白云母-斜长石-石英,其变质条件为t=570～598℃,P-0.7～1.0 CPa;绿帘角闪岩相在泥质岩石中的矿物组合为石榴石-黑云母-白云母-斜长石-绿泥石-石英,变质条件为t=518～545℃,P=0.5～0.8GPa;绿片岩相的矿物组合为白云母-绿泥石-石英-斜长石-(黑云母),其变质压力为0.6～0.65 GPa,温度可能为400～450℃。采用Spear提出的吉布斯方法,以石榴石变斑晶的环带变化得到高角闪岩相、低角闪岩相     

浙西南陈蔡群变质阶段划分及变质作用p—T—D轨变研究

按照构造变形不同阶段变质矿物生长发育特征，浙西南陈蔡群变质作用可分为四个阶段，变质阶段Ｉ与Ｄ１变形同期，变质矿物共生组合为绿泥石＋黑云母＋白云母＋斜长石＋石英，相当于绿片岩相变质；变质阶段Ⅱ发生于Ｄ１变形和Ｄ２变形这间的静态期，变质矿物共生组合为十字石＋石榴石＋斜长石＋石英＋黑云母＋白云母，变质温度范围为±５１０℃，压力为０．７ＧＰａ；变质阶段Ⅲ与Ｄ２变形同期或稍后，变质矿物共生组合为矽线石＋石榴     

浙西南陈蔡群变质阶段划分及变质作用p－T－D轨迹研究

按照构造变形不同阶段变质矿物生长发育特征，浙西南陈蔡群变质作用可分为四个阶段。变质阶段Ⅰ与Ｄ＿１变形同期，变质矿物共生组合为绿泥石＋黑云母＋白云母＋斜长石＋石英，相当于绿片岩相变质；变质阶段Ⅱ发生于Ｄ＿１变形和Ｄ＿２变形之间的静态期，变质矿物共生组合为＋字石＋石榴石＋斜长石＋石英＋黑云母＋白云母，变质温度范围为士５ｌ０℃，压力为０．７ＧＰａ；变质阶段Ⅲ与Ｄ＿２变形同期或稍后，变质矿物共生组合为矽线石＋石榴石＋斜长石＋石英＋黑云母＋白云母士钾长石，变质温度范围为６００～６５０℃，压力为０．５５～０．６５ＧＰ３；变质阶段Ｎ发生在Ｄ＿３或Ｄ＿３之后，变质矿物共生组合为绿泥石＋白云母，相当于低绿片岩相变质。根据构造变形不同阶段变质温度、压力变化所建立起来的ｐ－Ｔ－Ｄ轨迹，能够用来反映浙西南陈蔡群变质作用发生的构造环境。     

浙西南八都群泥质麻粒岩的变质演化与pT轨迹

浙西南古元古界八都群是目前华夏地块最古老的变质基底,以往研究认为其变质程度仅达角闪岩相。近来在对遂昌地区八都群富铝片麻岩的研究过程中,发现了具有"石榴石+夕线石+正/反条纹长石+黑云母"特征组合的泥质麻粒岩,表明该地体曾经历麻粒岩相变质改造。通过岩相学与矿物化学分析,确定该岩石经历了3个阶段的演化过程,即:早期进变质阶段(M1),形成"石榴石+黑云母+白云母+夕线石+斜长石+石英"的矿物组合;变质峰期阶段(M2-3),形成"石榴石+夕线石+三元长石+黑云母+石英"的矿物组合;峰期后降压冷却阶段(M4),形成"黑云母+白云母+新生斜长石+石英"的矿物组合。岩石中石榴石普遍发育与降温过程有关的扩散成分环带和与降压过程有关的斜长石后生合晶。通过石榴石-黑云母温度计和GASP压力计估算变质峰期的温压条件为800~850℃、0.6~0.7 GPa,峰期后退变质阶段的温压条件为560~590℃、0.25~0.33 GPa,具有顺时针样式的pT演化轨迹,反映一种陆壳碰撞增厚、后又拉伸减薄的动力学过程。     

含钙铝榴石的葡萄石—绿纤石相平衡：以新疆萨尔托海蛇绿岩中变基性岩石为例

利用矿物内部一致性热力学数据，建立了在ＣａＯ－Ａｌ２Ｏ３－ＭｇＯ－ＳｉＯ２－Ｈ２Ｏ体系中含钙铝榴石的葡萄石－绿纤石变质相平衡，确立了在葡萄石－绿纤石－钙铝榴石－绿帘石－绿泥石－石英组合中出现绿纤石－钙铝榴石共生、葡萄石－绿纤石共生、葡萄石－绿帘石共生和绿泥石－绿帘石－钙铝榴石共生的ＰＴ区间及其意义。根据该相平衡计算了新疆萨尔托海蛇绿岩中变基性岩石的葡萄石－绿纤石相变质ＰＴ条件为Ｔ＝３２５℃～３３５℃，Ｐ＝０．４５～０．４７５ＧＰａ。并讨论了Ｆｅ３＋＝Ａｌ替代对于形成钙铝榴石－绿纤石共生的影响。本文的研究表明，葡萄石－绿纤石－钙铝榴石－绿帘石－绿泥石－石英共生组合是葡萄石－绿纤石相中偏高压组合，钙铝榴石－绿纤石共生与绿纤石－阳起石相一样代表着葡萄石－绿纤石相中较高压相，钙铝榴石在葡萄石－绿纤石相中是可以稳定存在的。     

柴北缘锡铁山地体花岗质片麻岩退变质作用和40Ar/39Ar年代学研究及其地质意义

本文对柴达木盆地北缘锡铁山地区含榴辉岩透镜体花岗质片麻岩进行了系统的矿物学、相平衡模拟以及黑云母和石英⁴⁰Ar/³⁹Ar年代学研究,旨在查明花岗质片麻岩在加里东超高压变质之后,折返过程中发生角闪岩-绿片岩相退变质作用的变质条件和变质年代。矿物学和相平衡模拟显示,发育变形石英细脉的黑云母花岗质片麻岩高角闪岩相变质矿物组合(M1)为黑云母+钾长石+斜长石+石英+金红石+矽线石+钛铁矿,对应变质条件为T>620℃,P>0.16GPa;低角闪岩相-绿片岩相变质矿物组合(M2)为黑云母+白云母+斜长石+微斜长石+石英+榍石±绿泥石,变质条件为T=390～420℃和P=0.10～0.19 GPa。花岗质片麻岩中黑云母激光阶段加热⁴⁰Ar/³⁹Ar定年获得了一个上升的阶梯状表观年龄图谱,在中高温阶段则形成了一个平坦的表观年龄坪,坪年龄为353.9±1.8 Ma,对应的等时线年龄为356.7±5.6 Ma。变形石英脉样品真空击碎提取流体包裹体⁴⁰Ar/³⁹Ar...     

东准噶尔塔克札勒蛇绿混杂岩带变质作用特征

塔克札勒蛇绿混杂岩带的变质作用 ,具大洋水热变质、俯冲变质和区域低温动力变质作用的特征 ,其中以大洋水热变质作用为主。中志留世末洋盆扩张阶段 ,形成葡萄石、绿纤石相→低绿片岩相→角闪岩相的递增变质特征 ;早石炭世初洋壳向陆壳之下俯冲 ,俯冲变质作用不显著 ,仅见超镁铁岩具叶蛇纹石、纤维蛇纹石及绢石蚀变矿物 ;早石炭世中期塔克札勒有限洋盆开始粘连闭合 ,于晚石炭世早期褶皱造山 ,使蛇绿混杂岩带产生角闪岩相→高绿片岩相→低绿片岩相的退变质特征 ,使蛇绿岩带在辉长岩中由棕色角闪石退变为透闪石、阳起石和绿泥石、绢云母及绿帘石等变质矿物 ,是区域低温动力变质作用的产物 ,属低绿片岩相     

大陆造山带深熔垮塌的岩石学、地球化学证据:以北大别深熔混合岩为例

北大别位于大别造山带的核部,分布着大量的造山带垮塌时期形成的混合岩,其于理解大别造山带的形成和演化有着重要的意义。北大别混合岩的原岩为TTG（D）岩石,因黑云母和角闪石的脱水熔融诱发深熔作用产生。顺层产出的为富斜长石浅色体,主要矿物组成为斜长石+石英+黑云母±钾长石±角闪石。伟晶岩脉或团块为富钾长石浅色体,主要矿物组成为钾长石+石英±斜长石±黑云母±角闪石。暗色体为变晶结构,主要矿物组成为角闪石+黑云母+斜长石+石英±单斜辉石;其中,暗色矿物角闪石和黑云母常常定向排列,具有明显的溶蚀结构;暗色体中浅色矿物颗粒较小,以斜长石和石英为主,指示部分熔融的残余产物。全岩地球化学特征表明,碱金属元素（Na、K等）、大离子亲石元素（Ba、K、La等）和LREE等优先进入酸性熔体,而相容元素和中-重稀土元素等残留在残余体中。浅色体与本区花岗岩相比,二者都有右倾的稀土配分模式,富集LREE,亏损HREE。但浅色体具有明显的Eu正异常,δEu值为2.48~6.55,而花岗岩则有弱的Eu负异常,并且浅色体中大颗粒斜长石相互构成框架结构,含量明显高于正常花岗岩熔体,表明浅色体更可能是熔体早期结晶的产物。     

喜马拉雅造山带核部的变质作用与部分熔融:亚东地区高压泥质麻粒岩的岩石学与年代学研究

喜马拉雅造山带核部的高喜马拉雅结晶岩系是印度大陆深俯冲到欧亚板块之下经历了高压变质作用的产物,记录了喜马拉雅造山带的形成与演化历史。本文对喜马拉雅造山带中段亚东地区高喜马拉雅结晶岩系中的泥质麻粒岩进行了岩石学和锆石U-Pb年代学研究,结果表明泥质麻粒岩经历了复杂的变质演化和部分熔融,可识别出三期变质矿物组合。早期进变质矿物组合为石榴石+斜长石+钾长石+黑云母+白云母+石英,峰期变质矿物组合为石榴石+斜长石+钾长石+黑云母+蓝晶石+石英,晚期退变质矿物组合为石榴石+斜长石+钾长石+夕线石+黑云母+白云母+石英。相平衡模拟表明,该泥质麻粒岩经历了高温、高压的峰期变质条件为800~835℃和12.8~14kbar,在进变质和峰期变质过程中经历了白云母和黑云母脱水熔融,所形成的熔体量至少为5%~8%。麻粒岩的晚期退变质条件为720~740℃和7.6~8.3kbar。这表明泥质麻粒岩经历了一条以高压麻粒岩相峰期变质和降温、降压退变质为特征的顺时针P-T轨迹。锆石U-Pb定年结果表明,麻粒岩相变质和深熔作用发生在28.5~17.0Ma。本研究表明高喜马拉雅结晶岩系的上部构造层位经历了高压麻粒岩相变质作用,而不是以前认为的以高温、低压变质作用为特征,并为喜马拉雅造山带构造演化的研究提供了新的见解。     

Phase relations of biotite and stilpnomelane in the greenschist facies

Phase relations of biotite and stilpnomelane and associated silicate minerals have been studied in rocks of the greenschist facies, chiefly from Otago, New Zealand and western Vermont, but also from Scotland, Minnesota-Michigan iron range, and northwest Washington. That stilpnomelane in the greenschicht facies crystallizes initially with nearly all iron in the ferrous state is indicated by chemical analyses, high p-T experiments, and phase relationships. Alteration of stilpnomelane after metamorphism not only oxidizes iron but leaches potassium; corrections for both effects must be made in using analyses of brown stilpnomelane in studies of phase relations. Two discontinuous reactions which produce biotite at the biotite isograd have been identified:

1. muscovite+stilpnomelane+actinolite→ biotite+chlorite+epidote
2. chlorite+microcline→ biotite+muscovite. Biotite produced by the first of these reactions has a limited range of variation in Fe/Mg. As grade advances within the biotite zone more magnesian and ferruginous biotites become stable in consequence of the two continuous reactions:
3. muscovite+actinolite+chlorite→ biotite (Mg-rich)+epidote
4. muscovite+stilpnomelane→ biotite (Fe-rich)+chlorite.

Stilpnomelane is stable in muscovite-free rocks throughout the biotite zone, and even up to the grade at which hornblende becomes stable. Phengitic muscovite is stable throughout the biotite zone in New Zealand and thus apparently does not contribute to the formation of biotite until a higher grade is reached.     

Reactions to define the biotite isograd in the Ryoke metamorphic belt,Kii Peninsula,Japan

Two types of biotite isograd are defined in the low-grade metamorphism of the Wazuka area, a Ryoke metamorphic terrain in the Kii Peninsula, Japan. The first, BI₁, is defined by the reaction of chlorite+K-feldspar= biotite+muscovite+quartz+H₂O that took place in psammitic rocks, and the second, BI₂, by the continuous reaction between muscovite, chlorite, biotite and quartz in pelitic rocks. The Fe/Mg ratios of the host rocks do not significantly affect the reactions. From the paragenesis of pelitic and psammitic metamorphic rocks, the following mineral zones were established for this low-pressure regional metamorphic terrain: chlorite, transitional, chlorite-biotite, biotite, and sillimanite. The celadonite content of muscovite solid solution in pelitic rocks decreases systematically with the grade of metamorphism from 38% in the chlorite zone to 11% in the biotite zone. Low pressure does not prohibit muscovite from showing the progressive change of composition, if only rocks with appropriate paragenesis are chosen. A qualitative phase diagram of the AKF system relevant to biotite formation suggests that the higher the pressure of metamorphism, the higher the celadonite content of muscovite at BI₁, which is confirmed by comparing the muscovites from the Barrovian and Ryoke metamorphism.     

The Garnet+Hornblende Isograd in Calcic Schists from an Andalusite-Type Regional Metamorphic Terrain, Panamint Mountains, California

Calcic schists in the andalusite-type regional metamorphic terrainin the Panamint Mountains, California, contain the low-varianceassemblage quartz+epidote+muscovite+biotite+calcic amphibole+chlorite+plagioclase+spheneat low grade. Near the sillimanite isograd, chlorite in thisassemblage is replaced by garnet. The low variance in many calcicschists allows the determination of the nature of the reactionthat resulted in the coexistence of garnet+hornblende. A graphicalanalysis of the mineral assemblages shows that the reactioncan not be of the form biotite+epidote+chlorite+plagioclase+quartz=garnet+hornblende+muscovite+sphene+H₂Obecause garnet+chlorite never coexisted during metamorphismand the chlorite-bearing and garnet-bearing phase volumes donot overlap. The compositions of the minerals show that withincreasing grade amphibole changed from actinolite to pargasitichornblende with no apparent miscibility gap, the partitioningof Fe and Mg between chlorite and hornblende changed from K_D(Mg/Fe, chl&amp) < 1 to K_D > 1, the partitioning betweenbiotite and hornblende changed from K_D (Mg/Fe, bio/amp) <1 in chlorite-zone samples to K_D > 1 in garnet + hornblende-zonesamples, and the transition to the garnet-bearing assemblageoccurred when the composition of plagioclase was between An₅₅and An₈₀. Both the graphical analysis and an analytical analysisof the compositions of the minerals using simplified componentsderived from the natural mineral compositions indicate thatat the garnet+hornblende isograd the composition of hornblendewas colinear with that of plagioclase and biotite, as projectedfrom quartz, epidote, muscovite, and H₂O. During progressivemetamorphism, chlorite+biotite+epidote+quartz continuously brokedown to form hornblende+muscovite+sphene until the degeneracywas reached. At that point, tie lines from hornblende couldextend to garnet without allowing garnet to coexist with chlorite.Thus, the garnet+hornblende isograd was established throughcontinuous reactions within the chlorite-grade assemblage ratherthan through a discontinuous reaction. In this type of isograd,the low-grade diagnostic assemblage occurs only in Mg-rich rocks;whereas the high-grade assemblage occurs only in Fe-rich rocks.This relation accounts for the restricted occurrence of garnet+hornblendeassemblage in low-pressure terrains. In Barrovian terrains,garnet+chlorite commonly occurs, and the first appearana ofgarnet+hornblende can simply result from the continuous shiftof the garnet+chlorite tie line to Mg-rich compositions.     

Reactions leading to the formation and breakdown of stilpnomelane in the Otago Schist, New Zealand

Semi‐pelitic rocks ranging in grade from the prehnite–pumpellyite to the greenschist facies from south‐eastern Otago, New Zealand, have been investigated in order to evaluate the reactions leading to formation and breakdown of stilpnomelane. Detrital grains of mica and chlorite along with fine‐grained authigenic illite and chlorite occur in lower‐grade rocks with compactional fabric parallel to bedding. At higher grades, detrital grains have undergone dissolution, and metamorphic phyllosilicates have crystallized with preferred orientation (sub)parallel to bedding, leading to slaty cleavage. Stilpnomelane is found in metapelites of the pumpellyite–actinolite facies and the chlorite zone of the greenschist facies, but only rarely in the biotite zone of the greenschist facies. Illite or phengite is ubiquitous, whereas chlorite occurs only rarely with stilpnomelane upgrade of the pumpellyite‐out isograd. Chemical and textural relationships suggest that stilpnomelane formed from chlorite, phengite, quartz, K‐feldspar and iron oxides. Stilpnomelane was produced by grain‐boundary replacement of chlorite and by precipitation from solution, overprinting earlier textures. Some relict 14 Å chlorite layers are observed by TEM to be in the process of transforming to 12 Å stilpnomelane layers. The AEM analyses show that Fe is strongly partitioned over Mg into stilpnomelane relative to chlorite (K_D≈2.5) and into chlorite relative to phengite (K_D≈1.9). Modified A′FM diagrams, projected from the measured phengite composition rather than from ideal KAl₃Si₃O₁₀(OH)₂, are used to elucidate reactions among chlorite, stilpnomelane, phengite and biotite. In addition to pressure, temperature and bulk rock composition, the stilpnomelane‐in isograd is controlled by variations in K, Fe³⁺/Fe²⁺, O/OH and H₂O contents, and the locus of the isograd is expected to vary in rocks of different oxidation states and permeabilities. Biotite, quartz and less phengitic muscovite form from stilpnomelane, chlorite and phengite in the biotite zone. Projection of bulk rock compositions from phengite, NaAlO₂, SiO₂ and H₂O reveals that they lie close to the polyhedra defined by the A′FM minerals and albite. Other extended A′FM diagrams, such as one projected from phengite, NaAlO₂, CaAl₂O₄, SiO₂ and H₂O, may prove useful in the evaluation of other low‐grade assemblages.     

A Petrographic and Mineralogical Study of Volcanic Rocks from the Mayaxueshan Area, North Qilian Fold Belt, NW China

The Ordovician volcanic rocks in the Mayaxueshan area have been pervasively altered or metamorphosed and contain abundant secondary minerals such as albite, chlorite, epidote, prehnite, pumpellyite, actinolite, titanite, quartz, and/or calcite. They were denoted as spilites or spilitic rocks in terms of their petrographic features and mineral assemblages. The metamorphic grades of the volcanic rocks are equivalent to that of the intercalated metaclastic rocks. This indicates that both the spilitic volcanic rocks and metaclastic rocks in the Mayaxueshan area have formed as a result of Caledonian regional metamorphism. We suggest that the previously denoted spilitic rocks or altered volcanic rocks should be re-denoted as metabasalts or metabasaltic rocks. The metamorphic grade of the volcanic rocks increases with their age: prehnite-pumpellyite facies for the upper part of the Middle Ordovician volcanic rocks, prehnite-pumpeilyite to lower greenschist facies for the lower part of the Middle Ordovician vol     

Metamorphism, geochemistry and origin of magnesian volcanic rocks, Klamath Mountains, California

Metabasaltic rocks in the Klamath Mountains of California with ‘komatiitic’ major element concentrations were investigated in order to elucidate the origin of the magnesian signature. Trace-element concentrations preserve relict igneous trends and suggest that the rocks are not komatitic basalts, but immature arc rocks and within-plate alkalic lavas. Correlation of ‘excess’ MgO with the volume per cent hornblende (±clinopyroxene) suggests that the presence of cumulus phases contributes to the MgO-rich compositions. Early submarine alteration produced regional δ¹⁸O values of +10±1.5%_° and shifts in Al₂O₃, Na₂O, and K₂O concentrations. Regional metamorphic grade in the study area varies from biotite-zone greenschist facies (350–550°C, c. 3 kbar) southward to prehnite–actinolite facies (200–400°C, ≤3 kbar), but little isotopic or elemental change occurred during the regional recrystallization. The greenschist facies assemblage is actinolitic hornblende + phengite + epidote + sodic plagioclase + microcline + chlorite + titanite + hematite + quartz in Ti-poor metabasaltic rocks; in addition to these phases biotite is present in Ti-rich analogues. Lower grade greenstones contain prehnite and more nearly stoichiometric actinolite. The moderate to low pressures of regional metamorphism are compatible with P–T conditions in a magmatic arc. Later contact metamorphism at 2–2.9±0.5 kbar and at peak temperatures approaching 600° C around the English Peak and Russian Peak granodiorites produced 3–4–km-wide aureoles typified by gradual, systematic increases in the pargasite content of amphibole, muscovite content of potassic white mica, and anorthite content of plagioclase compositions. Metasomatism during contact metamorphism produced further increases in bulk-rock δ¹⁸O_SMOW of as much as +6%_°. Thus, the unusually MgO-rich nature of the Sawyers Bar rocks may be attributed at least partly to metasomatism and the presence of magnesian cumulus phases.     

Progressive sequence of reactions of the Ryoke metamorphism in the Yanai district, southwest Japan: the formation of cordierite

The compositions of biotite and muscovite were examined in terms of the paragenesis and the metamorphic grade in low- to medium-grade pelitic rocks of the Ryoke metamorphism in the Yanai district, southwest Japan. The biotite and muscovite that coexist with K-feldspar have a higher K component in an A'KF diagram than those in rocks lacking K-feldspar. This fact reflects an increase in the K₂O content in muscovite, but in biotite it reflects an increase of not only the K₂O content but also of the octahedral vacancy.
At higher metamorphic grade beyond the cordierite isograd, where cordierite coexists with neither chlorite nor K-feldspar, the biotite shows an increase in illite, K Aliv □xii−1 Si−1, and Tschermak components, Alvi Aliv R+−1 Si−1, where □xii and R+ denote the interlayer vacancy and (Fe+Mg+Mn), respectively. A reaction to define the cordierite isograd is proposed by treating this chemical change as being responsible for the first appearance of cordierite, i.e. K,Al-poor biotite+phengitic muscovite=K,Al-rich biotite+cordierite+quartz+water .By treating this as a key reaction in medium-grade metamorphism, a set of reaction in a progressive metamorphism is established for the Ryoke metamorphism, a typical low-pressure type metamorphism. Some textures in one of the high-grade areas, the K-feldspar-cordierite zone, suggest that a further two prograde reactions have taken place, i.e. andalusite+biotite+quartz=cordierite+K-feldspar+water
and   andalusite=sillimanite.quartz=cordierite+K-feldspar+water
This implies that this zone probably has a P–T  path involving isobaric heating.     

Petrology of an Andalusite-Type Regional Metamorphic Terrane, Panamint Mountains, California

The terrane in the Panamint Mountains, California, was regionallymetamorphosed under low-pressure conditions and subsequentlyunderwent retrograde metamorphism. Prograde metamorphic isogradsthat mark the stability of tremolite + calcite, diopside, andsillimanite indicate a westward increase in grade. The studywas undertaken to determine the effects of the addition of Caon the types of assemblages that may occur in pelitic schists,to contribute to the understanding of the stability limits inP – T – aH₂O – X_Fe of the pelitic assemblagechlorite + muscovite + quartz, and to estimate the change inenvironment from prograde to retrograde metamorphism. Peliticassemblages are characterized by andalusite + biotite + stauroliteand andalusite + biotite + cordierite. Within a small changein grade, chlorite breaks down over nearly the entire rangein Mg/(Mg + Fe) to biotite + aluminous mineral. Chlorite withMg/(Mg + Fe) = 0.55 is stable to the highest grade, and thegeneralized terminal reaction is chlorite + muscovite + quartz= andalusite + biotite + cordierite + H₂O. Calcic schists arecharacterized by the assemblage epidote + muscovite + quartz+ chlorite + actinolite + biotite + calcite + plagioclase atlow grades and by epidote + muscovite + quartz + garnet + hornblende+ biotite + calcite + plagioclase at high grades. Epidote doesnot coexist with any AFM phase that is more aluminous than garnetor chlorite. Lithostatic pressure ranged from 2.3 kb to 3.0kb. During prograde-metamorphism temperatures ranged from lessthan 400° to nearly 700°C, and X_H2O (assuming P_H2O +P_CO3 = P_total) is estimated to be 0.25 in siliceous dolomite,0.8 in pelitic schist, and 1.0 in calcic schist. Temperatureduring retrograde metamorphism was 450° ± 50°C,and all fluid were H₂O-rich. A flux of H₂O-rich fluid duringfolding is believed to have caused retrograde metamorphism.The petrogenetic grid of Albee (1965b) is modified to positionthe (A, Cd) invariant point relative to the aluminosilicatetriple point, which allows the comparison of facies series thatinvolve different chloritoid-reactions.     

The origin of biotite in archaean meta-sediments near Yellowknife,N. W. T., Canada

Data on mineral compositions, modal proportions and textural relations are used to deduce the biotite-forming reaction in Archaean meta-greywackes and meta-pelites of a low-pressure facies series. Biotite originated by reaction of chlorite, muscovite and ilmenite, producing rutile, K-feldspar and quartz as subordinate reaction products. Chlorite composition did not change as the reaction progressed but muscovite became depleted in K and (Mg+Fe+Mn) while gaining a little Ti. The composition of biotite produced in the meta-pelites is to some extent dependent on how much biotite was formed.     

Reaction softening by dissolution–precipitation creep in a retrograde greenschist facies ductile shear zone,New Hampshire,USA

We describe strain localization by a mixed process of reaction and microstructural softening in a lower greenschist facies ductile fault zone that transposes and replaces middle to upper amphibolite facies fabrics and mineral assemblages in the host schist of the Littleton Formation near Claremont, New Hampshire. Here, Na‐poor muscovite and chlorite progressively replace first staurolite, then garnet, and finally biotite porphyroblasts as the core of the fault zone is approached. Across the transect, higher grade fabric‐forming Na‐rich muscovite is also progressively replaced by fabric‐forming Na‐poor muscovite. The mineralogy of the new phyllonitic fault‐rock produced is dominated by Na‐poor muscovite and chlorite together with late albite porphyroblasts. The replacement of the amphibolite facies porphyroblasts by muscovite and chlorite is pseudomorphic in some samples and shows that the chemical metastability of the porphyroblasts is sufficient to drive replacement. In contrast, element mapping shows that fabric‐forming Na‐rich muscovite is selectively replaced at high‐strain microstructural sites, indicating that strain energy played an important role in activating the dissolution of the compositionally metastable muscovite. The replacement of strong, high‐grade porphyroblasts by weaker Na‐poor muscovite and chlorite constitutes reaction softening. The crystallization of parallel and contiguous mica in the retrograde foliation at the expense of the earlier and locally crenulated Na‐rich muscovite‐defined foliation destroys not only the metastable high‐grade mineralogy, but also its stronger geometry. This process constitutes both reaction and microstructural softening. The deformation mechanism here was thus one of dissolution–precipitation creep, activated at considerably lower stresses than might be predicted in quartzofeldspathic rocks at the same lower greenschist facies conditions.