利用X射线衍射测定单斜辉石中硬玉组分含量

硬玉是单斜辉石中十分重要的端元组分,是单斜辉石分类的主要基础。利用x射线衍射分析确定的硬玉组分含量计算式为Jd(％)=[A-2.235]×25.741,其中Jd为硬玉组分百分含量,A为2—Theta角为30°(d=2.97)时峰值的相对强度Ⅰ与半高宽的乘积,其计算误差仅6.32％。     

Origin of Grandite Garnet in Calc-Silicate Granulites: Mineral-Fluid Equilibria and Petrogenetic Grids

The role of clinopyroxene in producing grandite garnet is evaluatedusing data from an ultrahigh-temperature metamorphosed calc-silicategranulite occurrence in the Eastern Ghats Belt, India. ‘Peak’pressure–temperature conditions of metamorphism were previouslyconstrained from associated high Mg–Al granulites as c.0·9 GPa, >950°C, and the rocks were near-isobaricallycooled to c. 750°C. Grandite garnet of variable compositionwas produced by a number of reactions involving phases suchas clinopyroxene, scapolite, plagioclase, wollastonite and calcite,in closely spaced domains. Compositional heterogeneity is preservedeven on a microscale. This precludes pervasive fluid fluxingduring either the peak or the retrograde stage of metamorphism,and is further corroborated by computation of fluid–rockratios. With the help of detailed textural and mineral compositionalstudies leading to formulation of balanced reactions, and usingan internally consistent thermodynamic dataset and relevantactivity–composition relationships, new petrogenetic gridsare developed involving clinopyroxene in the system CaO–Al₂O₃–FeO–SiO₂–CO₂–O₂in T–aCO₂–fO₂ space to demonstrate the importanceof these factors in the formation of grandite garnet. Two singularcompositions in garnet-producing reactions in this system arededuced, which explain apparently anomalous textural relations.The possible role of an esseneite component in clinopyroxenein the production of grandite garnet is evaluated. It is concludedthat temperature and fO₂ are the most crucial variables controllinggarnet composition in calc-silicate granulites. fO₂, however,behaves as a dependent variable of CO₂ in the fluid phase. Externalfluid fluxing of any composition is not necessary to producechemical heterogeneity of garnet solid solution. KEY WORDS: grandite garnet; role of clinopyroxene; internal buffering; oxidation–decarbonation equilibria     

碱性玄武岩中的某些巨晶单斜辉石──Ⅱ:穆斯堡尔谱──兼论单斜辉石的异常穆斯堡尔谱和铁结构态的测定

本文对辽宁宽甸碱性玄武岩中巨晶单斜辉石进行穆斯堡尔谱研究。应用晶体结构研究结果较合理地解释了单斜辉石的异常穆斯堡尔谱。结合XRD讨论了单斜辉石中Fe结构态的测定以及穆斯堡尔谱的可应用性。巨晶应结晶于相当氧化的环境。     

阿尔泰南缘中泥盆统北塔山组火山岩的矿物学研究

阿尔泰山南缘中泥盆统北塔山组火山岩极为发育。本文对富辉橄玄岩和玄武岩中的单斜辉石和橄榄石斑晶进行了矿物化学分析,并结合矿物的地质温压计和岩浆结晶模拟,约束了两种岩石中矿物的形成过程,推测了原始岩浆的演化过程。提出富辉橄玄岩和玄武岩的原始岩浆属于拉斑玄武系列,富辉橄玄岩中的高压单斜辉石来源于深部（40～50 km）,其结晶早于橄榄石;玄武岩中单斜辉石大多属于岩浆房结晶产物（30～40km）,其结晶晚于橄榄石;两种岩石中橄榄石均属于岩浆房结晶产物（30～40 km）。     

Clinopyroxene REE Geochemistry of the Red Hills Peridotite, New Zealand: Interpretation of Magmatic Processes in the Upper Mantle and in the Moho Transition Zone

The Red Hills peridotite in the Dun Mountain ophiolite of SouthIsland, New Zealand, is assumed to have been produced in a paleo-mid-oceanridge tectonic setting. The peridotite is composed mostly ofharzburgite and dunite, which represent residual mantle andthe Moho transition zone (MTZ), respectively. Dunite channelswithin harzburgite blocks of various scales represent the MTZcomponent. Plagioclase- and clinopyroxene-bearing dunites occursporadically within common dunites. These dunites representproducts of melt–wall-rock interaction. Chondrite-normalizedrare earth element (REE) patterns of MTZ clinopyroxenes showa wide compositional range. Clinopyroxenes in plagioclase dunitesare extremely depleted in light REE (LREE) ([Lu/La]_N >100),and are comparable with clinopyroxenes in abyssal peridotitesfrom normal mid-ocean ridges. Interstitial clinopyroxenes inthe common dunite have flatter patterns ([Lu/La]_N 2) comparablewith those for dunite in the Oman ophiolite. Clinopyroxenesin the lower part of the residual mantle harzburgites are evenmore strongly depleted in LREE ([Lu/La]_N = 100–1000) thanare mid-ocean ridge peridotites, and rival the most depletedabyssal clinopyroxenes reported from the Bouvet hotspot. Incontrast, those in the uppermost residual mantle harzburgiteand harzburgite blocks in the MTZ are less LREE depleted ([Lu/La]_N= 10–100), and are similar to those in plagioclase dunite.Clinopyroxenes in the clinopyroxene dunite in the MTZ are similarto those reported from mid-ocean ridge basalt (MORB) cumulates,and clinopyroxenes in the gabbroic rocks have compositions similarto those reported from MORB. Strong LREE and middle REE (MREE)depletion in clinopyroxenes in the harzburgite suggests thatthe harzburgites are residues of two-stage fractional melting,which operated initially in the garnet field, and subsequentlycontinued in the spinel lherzolite field. The early stage meltingproduced the depleted harzburgite. The later stage melting wasresponsible for the gabbroic rocks and dunite. Strongly LREE–MREE-depletedclinopyroxene in the lower harzburgite and HREE-enriched clinopyroxenein the upper harzburgite and plagioclase dunite were formedby later reactive melt migration occurring in the harzburgite. KEY WORDS: clinopyroxene REE geochemistry; Dun Mountain ophiolite; Moho transition zone; orogenic peridotite; Red Hills     

徐淮地区镁铁质岩石捕虏体单斜辉石中石榴石和石英的出溶

徐淮地区早侏罗世侵入杂岩中榴辉岩,石榴辉石岩和单斜辉石岩捕虏体单斜辉石中可以观察丰富的出溶石英针和石榴石,黝帘石及角闪石的出溶叶片,榴辉岩中出溶石英针的绿辉石核部比其边部相对富含FeO和MgO,贫SiO2,Al2O3和CaO。在石榴辉石岩和单斜辉石岩捕虏体中具有出溶石榴石的单斜辉石。从靠近出溶石榴石的一侧向其核部,Al2O3,Na2O和TiO2含量降低,MgO,SiO2和CaO含量增加,单斜辉石中定向石英针的出溶表明曾经存在有超高压条件下（≥25×10^8Pa)稳定的过硅质绿辉石。单斜辉石中出溶石榴石表明温压条件的降低可能是引起出溶的一个主要原因,捕虏体中的矿物组合和岩相学特征表明它们曾经遭受了榴辉岩相和角闪岩相退化变质作用,这与因压力和温度降低引起矿物出溶的结果相吻合。     

雅鲁藏布江缝合带西段错不扎铬铁矿特征及形成环境

雅鲁藏布江蛇绿岩带是国内铬铁矿床出露点最多,且铬铁矿石储量、产量最大的一个蛇绿岩带。根据空间展布规律,该岩带被划分为东段(曲水—墨脱)、中段(昂仁—仁布)和西段(萨嘎至中印边境)3部分。其中,西段自萨嘎以西分为南、北两支亚带。长期以来的研究工作主要集中在东段和中段,西段的研究程度非常薄弱,尤其是北亚带。不同区段研究程度的不平衡十分不利于雅鲁藏布江蛇绿岩带内铬铁矿找矿工作的开展。错不扎蛇绿岩体位于雅鲁藏布江缝合带西段的北亚带,呈北西-南东向带状产出,主要由方辉橄榄岩组成,并普遍发育基性岩脉。野外地质调查在该蛇绿岩体中发现了多个铬铁矿化点,矿化体呈透镜状产于方辉橄榄岩中,出露地表的长度为0.5～1m,厚为0.2～0.5 m,矿石均为致密块状。电子探针分析结果表明,错不扎铬铁矿属于高铬型铬铁矿,铬尖晶石的Cr#[=100×Cr/(Cr+Al)]为75～78,Mg#[=100×Mg/(Mg+Fe2+)]为66～69。计算结果表明,母岩浆的FeO/MgO比值为0.51～0.65,Al2O3和Ti O2含量分别为11.27%～12.1%和0.19%～0.4%,与玻安质岩浆的化学成分相当。然而,针状单斜辉石出溶体的发现指示错不扎铬铁矿可能还经历了一个深部作用过程。     

西沙群岛基底火山碎屑岩中单斜辉石的矿物化学特征及其地质意义

本文利用电子探针对南海西沙群岛琛航岛珊瑚礁底部火山碎屑岩中的单斜辉石矿物的化学特征进行了研究。结果表明,该单斜辉石属于富钙透辉石,部分有正环带结构,从核部到边部Ca、Fe、Ti的含量逐渐增加,是岩浆正常结晶顺序的反映,说明该区域的岩浆演化是向着富Ca、Fe、Ti方向发展的。主量元素数据显示,单斜辉石具有低Si高Al的特征(SiO₂=41.40%～48.44%,Al₂O₃=5.54%～10.20%),且AlⅣ含量较高,说明母岩浆为不饱和碱性岩浆系列;此外,单斜辉石Ca含量偏高,Ca/(Ca+Mg+Fe)值在46.1%～51.4%之间,推测是母岩浆的高Ca含量导致了大量高钙辉石的产出。结合西沙海域的地震和构造资料,推测琛航岛珊瑚礁的基底是玄武质火山碎屑岩组成的平顶状海山,系岩浆穿过断裂发育的岩石圈层在西沙群岛的海底喷发,随后火山碎屑物质经过堆积、固结作用而形成;该火山碎屑岩的原岩为板内碱性玄武岩。     

Revised activity–composition models for clinopyroxene and amphibole

Recent activity–composition models for clinopyroxene and amphibole are revised to provide better consistency with observed phase relations in natural rocks. For clinopyroxene, the calibration in NCFMAS is retained, but the incorporation of acmite is revised to improve the partitioning of ferric iron between coexisting clinopyroxenes. For amphibole, the NCFMASH calibration is retained, but the addition of ferric iron is changed to provide consistency with the clinopyroxenes. The thermodynamics of orthoamphibole (gedrite) is also adjusted to resolve an unrelated inconsistency. The effects of these improvements are illustrated through comparison of calculated pseudosections produced with the existing and new models with natural data from lawsonite eclogites.     

Oxidation Experiment of Natural Megacrystal Clinopyroxene: Implications for Assignment of Mössbauer Spectra

The Mössbauer spectra of natural megacrystal clinopyroxene are usually fitted by 4 sets of symmetric doublets, A‐A', B‐B', C‐C' and D‐D', respectively, in terms of increasing Qs value in literature. But the assignments of those doublets are quite different, except the D‐D' doublet assigned to Fe³⁺at the lattice site M***1 in previous papers. Particularly, the assignment and interpretation of the C‐C' doublet are diverse. The oxidation experiments of natural megacrystal clinopyroxene collected from the Hannuoba basalt, North China, were performed under controlled conditions of temperature at 1000°C and oxygen fugacity of FMQ buffer in 1, 2, ***3 and 5 days respectively. The oxidized samples were then measured by X‐ray diffraction spectrometry and Mössbauer spectrometry. The oxidation of clinopyroxene is characterized by Fe²⁺ → Fe³⁺at M1 under the subsolidus conditions, which is consistent with the increase of the area of the D‐D' doublet when the heating time increases. Accordingly, the area of the A‐A' and B‐B' doublets decreases with the increasing heating time. However, the area of C‐C' keeps almost constant. Therefore, the 4 sets of doublets can be assigned correctly as follows: A‐A' doublet to Fe⁺²at M1, B‐B' Fe²⁺at M1, C‐C' Fe²⁺at M2, and D‐D' Fe³⁺at M1. The M1 site splitting is due to the NNN (Next Nearest Neighbour) effect of the M2 site. The amount of Fe³⁺at the tetrohedral site of megacrystal clinopyroxene is negligible according to this study.