胶东金矿床围岩蚀变带内云母类矿物、矿物化学-多型系列及其找矿信息

对胶东15个金放床围岩蚀变带内30个云母类矿物的地质产状，空间分带，与矿化关系地质调查基础上，着重对各类型金矿床蚀变带内云母类矿物进行了单矿物提纯，矿物化学定量分析，物理性质鉴定，X光衍射分析，差热分析，红外吸收光谱分析，晶格常数计算，形成条件等方面的系统研究，确定了蚀变岩带内有9种云母类矿物，5个矿物化学－多型系列，新鉴定出5种云母类矿物，绿鳞石（Celadonite),铁绿鳞石（Ferian Celadonite)，铁铝绿磷石（Ferian-Alumino Celadonite)，铝绿鳞石（Alumino Celadonite)和伊利石（Illite)，总结了云母类矿物各系列的演化特征，查明了金矿床各蚀变－矿化带内所出现的云母类矿物晕，指出了各云母类矿物晕的找矿信息。     

云母类矿物的活化释钾性能

通过对３个典型二八面体型的云母类矿物,即白云母,绢云母和伊利石的活化释钾试验,发现云母类矿物热自理产物酸化后钾能大量释放;探讨了云母类矿物的活化释钾性能。虽然白云母释钾的活化条件相对较高压有利于晶包有机质释放但其释钾量明显大于绢云母和伊利石。     

一株产铁载体细菌的筛选及其与云母的相互作用

        产铁载体细菌与云母类矿物相互作用的研究有助于了解矿物生物风化和土壤形成的演化规律和机理。采用纯培养法 自南京龙山废钾矿区酸模根际土壤分离筛选到一株高产荧光铁载体的细菌Z6,通过16S rDNA 序列分析和生理生化反应将其 鉴定为假单胞菌属（Pseudomonas sp.）;通过室温静置培养试验研究Z6 菌株与云母的相互作用结果表明,细菌生长代谢前期 （8~15 d）快速产生大量铁载体,菌株与矿物共培养75 d 后,产铁载体细菌对云母类矿物确实产生了风化作用,黑云母组发 酵液中Fe 含量增加了211 倍,Si 含量增加了约27.8 倍,SEM 显示云母表面出现溶蚀坑,细菌可以在矿物表面形成生物膜或 矿物- 细菌复合物。不同矿物对共培养体系中细菌数量、荧光铁载体含量、溶液pH 的影响不同。     

云母类粘土矿物的研究及其地质意义

云母类粘土矿物的研究及其地质意义刘云（中国科学院南京地质古生物研究所，江苏南京，２１０００８）关键词云母类粘土矿物，红外谱线变化，矿物学研究，地质意义铝二八面体云母类粘土矿物是蒙脱石一伊利石、蒙脱石混层一伊利石系列的一个过渡型矿物，在沉积岩中广泛分布...     

试论含钾岩石的农业直接应用

根据前人直接应用含钾岩石的成功经验；土壤中供钾矿物和含钾岩石中含钾矿物的相似性，土壤中含钾矿物的有效性和含钾岩石供钾潜力的研究结果，本文论述了组成矿物的有效性和含钾岩供钾潜力的研究结果，本文论述了组成矿物主要为云母类矿物的含钾岩石，农业直接应用可能具有良好效果。     

云母矿物材料研究现状及前景

详细介绍云母类矿物的工艺，物理性质及其主要应用方向，提出开发利用前景。     

应用X射线衍射-扫描电镜-光学显微镜鉴定黑龙江石墨尾矿中的绢云母

石墨尾矿作为一类二次资源,当云母类矿物的含量在10%以上时,具有回收利用价值。黑龙江某地石墨尾矿中含有10%以上的云母类矿物,但其细度(500~800目)低于常规的云母矿,本文采用X射线衍射(XRD)分析矿物组成,再结合化学分析、扫描电镜-能谱、光学显微镜与纯矿物进行对比,由此鉴定云母类矿物种属。XRD研究初步表明石墨尾矿含有的云母族矿物属于白云母亚类或黑云母亚类。扫描电镜分析表明尾矿中的云母矿物与纯绢云母矿物均以片状和鳞片状为主要存在形态,而纯黑云母主要以片状形式存在。尾矿的Si O2含量为5%~13%,Al2O3含量为4%~8%,与纯绢云母接近。光学显微镜鉴定显示在正交偏光下石墨尾矿中的云母颜色和纯绢云母类似,而与纯黑云母截然不同。综合以上结果最终可确定该地石墨尾矿中的云母族矿物为白云母亚类中的绢云母。本研究为后续石墨尾矿的选矿工艺奠定了基础,也可应用于类似细度绢云母的鉴定。     

云母族中白云母亚族扩展为铬铝云母亚族

通过详细研究世界范围内1842—1993年他人76个及作者42个含Cr的且与白云母同结构的云母化学成分资料,确立了自然产出的云母族矿物结构层内八面体中Cr~(3+)与Al~(3+)的完全类质同象关系。重新核查了云母族矿物分类,强调了按云母族矿物结构层内,八面体位置上所占据的阳离子类型,及其类质同象程度进行亚族划分的原则,将过去的二八面体型Al系列即白云母亚族,扩充为Cr—Al系列即铬铝云母亚族     

白云鄂博矿床氟金云母的矿物学研究

内蒙白云鄂博REE-Nb-Fe矿床广泛分布的“金云母”,以F含量〉〉H2O^＋含量为其鲜明特色。按∑（O＋F）=12计算的金云母化学式表明,其附加阴离子中,绝大多数F〉OH。根据国际矿物协会（IMA）新矿物及矿物命名委员会（CNMMN）的规定,F〉OH（离子摩尔数）的金云母,应称氟金云母,属云母族的独立矿物种。检索IMA CNMMN公布的已知矿物种名录,均无氟金云母条目。为此,按新矿物要求,对该矿物作了详尽而系统的矿物学研究;同时还对金云母组的矿物作了分类。     

航空高光谱识别的高、中、低铝绢云母矿物成因学研究

国内外学者在航空高光谱矿物填图时,根据Al-OH光谱特征吸收波长位置不同将浅色云母类矿物分为2~3类,分别命名为高铝绢云母、中铝绢云母、低铝绢云母,但对它们的成因特点却只有零星的讨论,没有比较系统的有针对性的研究。本文在新疆雪米斯坦铀多金属成矿带获取CASI/SASI航空高光谱数据,并开展矿物填图的基础上,针对高铝绢云母、中铝绢云母、低铝绢云母等三种矿物的成因学专门开展了比较系统的研究。采用的方法主要是在开展详细的野外地质观察、采样的基础上,对采集的上述三类矿物蚀变岩样品进行详细的室内光谱测量、Al-OH吸收波长位置统计、显微薄片观察、全岩X衍射分析、粘土X衍射分析等研究,并结流体成矿理论和已有矿物成因学知识,进行了详细深入的分析讨论。研究表明,高铝绢云母蚀变岩蚀变强烈,云母类蚀变矿物以绢云母、伊利石为主,且主要与叶腊石和微晶石英等矿物伴生,而低铝绢云母蚀变岩蚀变强度中等,以伊利石、伊蒙混层为主,绿泥石增加,主要与方解石、浊沸石等矿物伴生;高铝绢云母蚀变岩具有相对高的石英含量和粘土矿物总量,具有相对较低的钾长石、斜长石以及方解石含量;低铝绢云母蚀变岩则具有相对较低的石英和粘土含量,具有相对较高的斜长石、钾长石和方解石含量。通过深入分析讨论,本文提出了在研究区航空高光谱识别的高铝绢云母形成于相对高温、偏酸性的热液流体环境,低铝形成于相对低温、偏碱性的热液流体环境。这一新认识对航空高光谱遥感矿物填图结果的深入应用和深层次找矿信息反演具有重要意义。     

云母的命名

定义云母为层状硅酸盐。其结构单元由两个相向排列的四面体片（Ｔｓ）和夹于其间的一个八面体片（Ｏｓ）组成。这些片构成一个单元层,层与层之间被非水化层间阳离子（Ｉ）分开,其顺序是：非水化阳离子层、四面体片、八面体片、四面体片、非水化阳离子层、四面体片、八面...     

藏东及邻区钾玄岩系岩石云母特征及其岩石学意义

青藏高原东部及邻区新生代钾玄岩系列岩石包括钾质碱性深成岩、火山岩、煌斑岩和偏酸性的斑岩。云母是钾玄岩系列岩石中的主要暗色矿物，分布亦较广泛。我们用单矿物化学分析方法测定本区钾玄武岩系四种岩石中云母和化学成分，其结果MF＝1．30－1．99，应为金云母－富镁黑云母，属于富碱富镁高铝贫铁类型的云母；云母的红外光谱，在450cm^-1和1000cm^-1附近都有很强的吸收谱带，显示了四种岩石中的云母具有类似的红外光谱特征；X光衍射测定，本区云母的d(060)为15．32nm-15.41nm，它们的晶胞参数变化不大，均为三八面体1M型云母。以上特征表明，本区钾玄岩系四种岩石中云母均形成于高碱度环境，它们与钙碱性系列岩石中云母形成的环境迥然不同。从四种岩石的云母具有相似的化学成分、红外光谱和晶胞参数，说明它们的寄生岩石具有钾岩的特征，其物源来自交代地幔。     

Zoning and recrystallization of phengitic micas: implications for metamorphic equilibration

White micas (phengites) in the metasediments of the Scottish Dalradian display a large range of compositions within single samples. The variations in the composition of these phengites are strongly controlled by their structural age, with early fabrics containing a paragonite-poor, celadonite-rich phengite whereas in later fabrics the micas are generally paragonite-rich and celadonite-poor. Retrograde phengite growth, identified using back scattered electron imaging, occurs as celadonite-rich rims on micas within all existing fabrics and appears to be preferentially developed along existing white mica-plagioclase grain boundaries. The presence of these chemically distinct phengite populations within single samples implies that chemical exchange between the individual micas was inefficient. It is proposed that diffusion-controlled exchange reactions in phengites have relatively high closure temperatures below which major element exchange is effectively impossible. This closed system behaviour of micas questions the ease with which phengites may equilibrate with other phases during prograde greenschist and lower amphibolite facies metamorphism. Many of the chemical variations preserved in phengites from such metamorphic rocks may reflect deformation/recrystallization controlled equilibria.     

Volatile contents of phlogopite micas from South African kimberlite

Phlogopite micas from nodules in South African kimberlites were analyzed for major elements with the electron microprobe and for volatile contents by high temperature mass spectrometry. The micas are from primary- (deformed) and secondary- (undeformed) textured grains in perodotite xenoliths, glimmerites, MARID (mica-amphibole-rutile-ilmenite-diopside) suite nodules and a mica megacryst. The major element and volatile contents of micas exhibiting these modes of occurrence overlap to a greater extent than indicated in previous studies. Concentrations of volatile species occupying structurally defined crystallographic sites (H₂O, F, Cl) are greater for many of the micas than predicted on the basis of the mica formula, particularly for the glimmerite and MARID suite samples. A correlation exists between micas with tetrahedral and octahedral cation deficiencies and those with excess H₂O, F and Cl. Substitution of H⁺ for tetrahedral and possibly octahedral cations may be responsible for the excess H₂O in these micas. Except for one sample, the major element and volatile data for the peridotite, glimmerite and MARID suite micas indicate that they crystallized at oxygen fugacities below the quartz-fayalite-magnetite buffer. F and K₂O are in the correct proportion in the micas to provide the source for these elements in alkali basalts, but not in mid-ocean ridge basalts. Kaersutite amphibole is a more likely source of potassium and fluorine in mid-ocean ridge basalts.     

Sector-zoned phlogopites in igneous rocks

Sector-zoned micas are described in three occurrences of igneous rocks. Basal sectors (001) and lateral sectors (010) are well defined. Analyses of probably isochronous growth points indicate that there are consistent chemical composition differences between the sectors, the (010) sector being richer in Si and poorer in Ti, Fe, Al and Ba relative to the (001) sector. Within each sector type Fe/ (Fe + Mg) increases from core to rim. These differences vary in amplitude from one occurrence to the other, but are systematic for micas with extremely different tetrahedral cations. Possible factors influencing this type of crystallization are briefly reviewed: growth rate, geometry of protosites and bulk composition of the liquid.     

On micas from magmatic and metamorphic rocks

Micas from magmatic and metamorphic rocks differ from one another in chemical composition and in trace element content. The chemical composition of micas is discussed in relation to their occurrence, paragenesis and sequence of crystallization. On the basis of previous studies of the relationship between the physical properties and the chemical composition of 34 chemically analysed micas, reliable physical methods have been established which permit identification of different mica varieties in the same rock. Structural formulae and trace element content of micas from basic and granitic rocks, as well as from skarns, schists, ortho- and paragneisses are discussed. The relationship between the components of the tetrahedral and octahedral layers and of the interlayer are illustrated as ratios. Poorly differentiated, hybrid and metasomatic rocks often contain more than one variety of mica. Some prophyritic basalts and lamprophyres contain an early phlogopite which is paragenetically related to pyroxene phenocrysts and late biotite which occurs in the groundmass and in the fractures as a result of the crystallization of residual magma. The biotitemuscovite assemblage was observed in granodiorites, quartz-monzonites, schists and gneisses. In the albite-K-feldspar granites, muscovite predominates and the biotite is usually altered. The chemical composition of micas from metamorphic rocks depends on the grade of metamorphism and on the nature of associated minerals. The biotite from paragneisses contains considerable quantities of octahedral alumina. Pre-metamorphic micas show variable deficiencies of the (OH, F) group. The micas are useful minerals in determining the degree of differentiation and subsequent alteration of igneous rocks. The present study was carried out on the basis of 34 recent complete chemical analyses andca 100 X-ray fluorescence analyses. Dedicated to Professor Dr.Carl W. Correns on the occasion of his 70th birthday.     

Chemical Features of White Micas from the Piemonte Calc-schists, Western Alps and Implications for K–Ar Ages of Metamorphism

Anomalously large chemical ranges in muscovite-paragonite and muscovite-celadonite systems are observed in white micas from the Piemonte calcschists in the Chisone valley area, internal western Alps. The petrographical and chemical observations on white mica strongly suggest that most mica crystals with high Na/K ratios in the chlorite zone are of detrital origin, and were derived from the pre-Alpine high-temperature metamorphic sequence such the Caledonian and/or Variscan. Submicroscopic muscovite (Ms) - paragonite (Pg) composite aggregates occur in the chlorite zone and their EPMA analyses give an apparent chemical composition range from Ms_0.6Pg_0.4 to Ms_0.2Pg_0.8. In the rutile zone, the paragonite content of the white micas is less than 20%, suggesting that the white micas have been homogenized during the Alpine metamorphism even if detrital white micas existed.Metamorphic mica is also very heterogeneous. The total range in Si content becomes wider with increasing of metamorphic grade: 3.22–3.39 pfu for the chlorite zone, 3.07–3.45 pfu for the chloritoid zone and 3.06–3.59 pfu for the rutile zone. This clearly indicates that the micas have experienced significant retrogressive chemical reactions during cooling and exhumations of the host schists.The detrital white mica in the chlorite zone has not reset well in its K-Ar system during the Alpine subduction-related metamorphism. The wide range of the white mica K-Ar ages from 115 to 41 Ma must be due to a mixture of various amounts of detrital white mica in the separates. This feature is also observed in the chloritoid zone though the age variation is not so large as that in the chlorite zone. In contrast, the mica in the rutile zone, which was higher than 450°C, has been reset completely during Alpine HP metamorphism.     

LASER PROBE ~(40)Ar/ ~(39)Ar DATING OF MICAS ON THE DEFORMED ROCKS FROM ALTYN FAULT AND ITS TECTONIC IMPLICATIONS,WESTERN CHINA

LASER PROBE ~(40)Ar/ ~(39)Ar DATING OF MICAS ON THE DEFORMED ROCKS FROM ALTYN FAULT AND ITS TECTONIC IMPLICATIONS,WESTERN CHINAtheNationalNaturalScienceFundCommittee (NO .4 9772 157)     

The biotite isograd, Central Pyrenees: a deformation-controlled reaction

The biotite isograd reaction in Cambro–Ordovician pelites from the Garonne dome in the Central Pyrenees involves the production of biotite at the expense of chlorite, and the gradual reduction in the celadonite (Si) content of individual white micas. The mineral assemblages in the biotite-bearing rocks in the Melles area retain abundant evidence of chemical disequilibrium, due to the sluggish nature of major element diffusion within the white micas. The progress of the isograd reaction is strongly controlled by the progressive development of regional Variscan fabrics, and chemical exchange in the white micas in these metamorphic conditions is only possible during active deformation. Chemical resetting of the white micas takes place via the development of compositional zoning in the deforming micas; this probably occurs as a consequence of the introduction of defects and dislocations, causing more efficient diffusion within parts of individual grains. In the absence of deformation, this biotite isograd reaction would take place at significantly higher temperature and be controlled by the relatively high closure temperature of major element diffusion in white micas. Thus, assigning thermal significance to such continuous isograd reactions is impossible without independent constraints: kinetic factors such as deformation may be the dominant influence in many cases, not the thermodynamic controls.     

与盐构造相关的流体流动和油气运聚

盐构造的形成必然伴随着流体的活动 ,盐构造和流体构成了一个有机的反馈系统。含盐盆地中主要的流体类型有含盐热流体、烃类流体、富金属热流体及同生水和大气水等。盐构造在流体流动中起着重要的作用 :( 1)改造流体动力系统 ,包括密度驱动和超压驱动 ;( 2 )提供复杂的流体流动的通道网络 ,主要由盐丘上部的地堑式断裂簇和流体底辟通道、盐体 /围岩接触断裂等构成 ;( 3 )规定流体流动域———特定的流体赋存的特定的空间 ;( 4 )捕获流体共同运动。对于油气而言 ,盐构造既提供了油气运移的驱动力和运移通道 ,又提供了丰富的圈闭。在此基础上文中概括了盐构造、流体流动及油气运移和聚集相互关系的模式。地震剖面上的特征反射、岩心中的脉体、流体包裹体以及流体的理、化参数的空间变化等 ,可以帮助示踪与盐构造相关流体的流动路径 ,追溯流体流动的历史 ,认识油气成藏的过程。