内蒙古西乌珠穆沁旗阿木山组海绿石的特征及其沉积环境

在内蒙古西乌珠穆沁旗晚石炭世—早二叠世阿木山组第三段泥晶灰岩中发现有海绿石。对海绿石的微观特征分析表明,阿木山组海绿石呈团粒状结构,同时呈胶体产出于方解石周边,显示了原生海绿石的基本特点。电子探针的组分分析表明,阿木山组中的海绿石为高成熟度的海绿石。通过对不同地区和不同环境下海绿石的组分特征分析,建立了一种海绿石沉积的理想模式,同时揭示了阿木山组第三段海绿石化作用是在含氧量不够充分的弱还原状态下的正常浅海中进行的。本区阿木山组的下碎屑岩段和上灰岩段是在海水两进两退环境下的沉积,阿木山组灰岩中发现的海绿石则有可能代表了一个海进的开始。本区海绿石的发现及研究,对于进一步研究该区层序地层特征、地层格架及区域地层对比具有重要意义。     

陕北三叠系上统延长油层中海绿石的发现及其初步研究

本文对陕北三叠系延长群延长油层中的海绿石——延长海绿石进行了分析研究。结果表明,延长海绿石的矿物学特征与一般海绿石相同,其扩展层含量19%,属于无序低钾云母型结构。碳同位素及微量元素分析表明,延长海绿石系陆相淡水-半咸水湖泊环境下的自生矿物,延长海绿石存在于湖泊三角洲前缘远沙坝或三角洲间湖湾的粉-细砂岩中,也常与自生黄铁矿共生,其形成时水深为50-100m。海绿石的存在指示着该处为弱还原环境,对于成油较为有利。因此,在陆相湖泊三角洲环境中,也应当建立海绿石地球化学相。     

华北中南部地区石盒子群沉积环境研究新进展

华北地区石盒子群的沉积环境长期以来一致存在较大的争议,大多数研究者认为该时期完全为陆相沉积,也有一些学者在该地层中发现了海相沉积物。本文着重对鲁西、河南等地区石盒子群的奎山砂岩进行岩石学、沉积学、地球化学等指标研究,在该砂岩中发现了冲洗交错层理,并在该砂岩中上部发现了海绿石的存在。通过详细分析奎山砂岩中海绿石的显微特征、元素地球化学特征,并进行比较研究发现,华北地区奎山砂岩中海绿石的化学成分、含量与国内外古代的海相、过渡相海绿石基本一致,推断其为滨浅海富氧环境的产物。华北地区奎山砂岩中发育的沉积构造和所含海绿石的元素地球化学特征,揭示了该时期曾发生过海侵,反映了石盒子群沉积期沉积环境的复杂性。华北地区石盒子群奎山砂岩中上部海相沉积环境的确定,可能改变华北盆地二叠纪以来单纯为陆相沉积的认识,这为精细研究华北地区中晚二叠世的盆地格局、充填演化及恢复古地理景观,提供了新的思路和重要依据。     

藏西南札达白垩纪Albian期海绿石的矿物学特征及地质意义

海绿石是海相沉积的指相矿物,通常形成于海进系列,与低的沉积物供应速率有关。本文利用岩相和扫描电子显微镜(SEM)对样品进行了详细的观察,并运用X射线粉晶衍射(XRD)、傅立叶变换红外吸收光谱(FTIR)、电子探针微分析(EPMA)等技术,对藏西南札达县波林地区夏拉剖面中的海绿石砂岩和含海绿石灰岩样品进行了系统的分析与研究。上述分析表明砂岩和灰岩中的海绿石均为高演化的海绿石,砂岩中的海绿石为原地海绿石,而灰岩中的海绿石则源于下伏砂岩。通过沉积环境分析和区域地层对比,笔者等认为札达地区砂岩中海绿石的出现可能与Albian晚期印度大陆从澳大利亚—南极大陆的彻底裂解而造成的该地区的海进有关。持续的海进过程导致了该地区高演化的海绿石的形成。     

松辽盆地南部砂岩中的绿鳞石

本文对松辽盆地南部泉头组砂岩中的绿鳞石进行了较为系统的鉴定。并从绿鳞石的地质分布及产状入手,对其成因进行探讨。     

含铀海绿石

海绿石是海相沉积中一种分布很广的自生矿物。某些地质文献提到了海绿石中含有许多如:Ca、P、Ba、Li等元素的少量杂质。但是,尚未见到有关海绿石中含铀的资料。我们发现的含铀海绿石产于白垩纪滨海沉积物内。在不同程度富集铀的围岩里,海绿石中铀含量有所增高。其中一个研究地段的围岩由滨海相和浅海相砂岩、粉砂岩及粘土岩组成,它们都含有海绿石,但是,砂和砂岩中海绿石最发育,在粘土岩中海绿石的含量显著减少。海绿石具有肾状、稜角状和片状三种形态。海绿石的颗粒通常大于陆源沉积物的颗粒,其颗粒大小在0.06—0.36毫米范围内。海绿石所有变种的颜色主要从浅绿色到暗绿色,有时甚至是黑色,具有显微集合体消光,多色性从稻草黄     

天津蓟县中元古界铁岭组叠层石灰岩中原地海绿石的沉积学意义

天津蓟县剖面中元古界铁岭组二段叠层石灰岩中普遍发育海绿石。野外观察表明,海绿石主要分布在叠层石柱体间的泥晶灰岩中,呈薄膜状富集在叠层石鞘外缘;微观特征分析表明,海绿石呈不规则状的胶体形式,显示了原地海绿石的基本特点。电子探针的组分分析表明,铁岭组中的海绿石为中成熟度的海绿石。由于产在潮下高能柱状叠层石灰岩中,铁岭组中的海绿石并不反映低沉积速率或沉积间断的沉积条件,与现代海绿石的形成环境具有明显的差异。因此,中元古界铁岭组叠层石灰岩中的中成熟度原地海绿石是特殊沉积背景下的独特产物,为研究海绿石在地质历史时期产出的多样性提供了一个重要实例。     

中元古代晚期浅海高能沉积环境中的海绿石:以天津蓟县剖面铁岭组为例

海绿石是一种富钾、富铁的含水层状铝硅酸盐矿物,在沉积学领域常被作为一种普遍的指相矿物。多年研究的结果表明,现代海绿石主要形成在慢速、弱还原的较深水环境中,而且还可以作为"凝缩段"的识别标志之一。天津蓟县剖面中元古界铁岭组第二段灰岩中的海绿石,产在高能叠层石岩礁之中,主要以胶体形式富集在叠层石和均一石的边界上,代表较为典型的原地海绿石;较高的氧化钾含量(大于8%)而显示出高成熟海绿石的特点。很明显,铁岭组二段灰岩中的原地高成熟海绿石,不但不能作为"凝缩段"的识别标志,而且也不是长时间地层间断的产物。由于形成在正常高能浅海环境,而且处于中元古代末期,与现代沉积中的海绿石存在较大的差异,可能代表了中元古代末期的正常浅海还处于含氧量不够充分的弱还原状态,最终使铁岭组灰岩中的海绿石成为前寒武纪海绿石产出的一个典型代表,也间接的表明了在漫长的地质历史演变过程中海绿石产出的多样性特点。     

京津地区铁岭组,景儿峪组海绿石^40Ar—39Ar年龄

利用海绿石＾４０Ａｒ－＾３９Ａｒ年龄校正公式，通过测量海绿石中的可膨胀层含量ｎ以及中子活化过程中＾３９Ａｒ的丢失率η，求出海绿石的年龄。经测定，京津地区铁岭组，景儿峪组海绿石中可膨胀层含量为５％￣６％，中子活化中＾３９Ａｒ丢失率为１７％￣１９％，由校正后的海绿石年龄推测出铁岭组年龄界限范围。     

贵州二迭纪地层中海绿石矿物的发现及其地质意义

笔者发现的贵州晴隆二迭系中的海绿石矿物,经测试和鉴定,认为晴隆海绿石矿物是在滨海环境中形成。晶体结构为有序高钾云母型结构类型,矿物结构属于二八面体型类型,中等成熟度,含膨胀层小于或等于10％.从而推测与它有关的峨眉山玄武岩在该地的早期喷发环境亦应为滨海环境.     

Nature of the structural and crystal-chemical heterogeneity of the Mg-rich glauconite (Riphean,Anabar Uplift)

The detailed mineralogical and structural-crystal-chemical characteristics are reported for the first time for glauconite grains extracted from the fine-platy silty-sandy dolomites at the roof of the lower subformation of the Yusmastakh Formation (Riphean, Anabar Uplift, North Siberia). Based on the complex study (X-ray diffraction, classical chemical analysis, microprobe analysis, IR-spectroscopy, thermogravimetric analysis, scanning electron microscopy with microprobe analysis, and Mössbauer spectroscopy), it was demonstrated that the studied glauconite sample is characterized by unique chemical and structural heterogeneity.The mineral structure consists of micaceous (90%), smectite (6%), and di-trioctahedral chlorite (4%) layers. Mica is classed with Al-glauconite (Al > Fe³⁺) with elevated Mg content. The elevated Mg mole fraction of the mineral is caused by the presence of Mg-bearing brucite-type interlayers of di-trioctahedral chlorite and the high Mg content in the octahedral sheets of 2: 1 layers. It was first discovered that glauconites are characterized by the heterogeneous distribution of cations over the available trans- and cis-octahedra due to the coexistence of trans- and cis-vacant octahedra and small trioctahedral clusters in octahedral sheets. The distribution of isomorphic cations over the accessible octahedral sites is also heterogeneous due to the tendency of Fe, Mg and Al, Mg cations to segregation and formation of corresponding domains.It was found that structure of the studied glauconite has a specific stacking defect: in addition to the predominant subsequent layers of similar azimuthal orientation according to 1M type (～77%), some layer fragments are rotated at 180° (～15%) and ±120° (8%). The structural-crystal-chemical heterogeneity of the mineral is explained by the fact that its microcrystals grew in the dolomitic sediment under nonequilibrium conditions of the reduction zone of a shallow-water basin with a sufficiently high content of Mg cations, which significantly contributed to the glauconite formation.     

Saponite and celadonite in layer 2 basalts,DSDP Leg 37

Detailed examination of igneous core recovered during Leg 37 of the DSDP, has revealed that basalt diagenesis, an alteration effect resulting from low temperature interaction with seawater, is pervasive to depths of greater than 600 meters in layer 2. Phyllosilicates are among the main components of this low grade alteration effect and occur exclusively as saponite, celadonite and interlayered mixtures of these two phases. Saponites fall into two chemical groups as (a) Mg rich-Fe poor types characteristic of oxidative diagenesis and (b) Fe rich-Mg poor types characteristic of non-oxidative diagenesis. Celadonite is entirely restricted in occurrence to the oxidative diagenetic environment (oxidation halos) and rarely, if ever, occurs as a pure phase. In this respect, X-ray and electron microprobe analyses suggest the presence of interlayered smectite in some cases and iron-oxide contamination in others.Phyllosilicates generated during oxidative diagenesis of basalt occur in discrete mineralogical zones, typically arranged in the sequence Fe³⁺-oxide, celadonite, saponite proceeding outwards from a vein. The generation of these zones are modelled in terms of an infiltration dominated metasomatic process and their occurrence reflects a gradual extraction of oxygen from inflowing seawater during progressive reaction with the massive crystalline basalt.Mass balance calculations applied to the oxidative diagenetic process suggest that a source external to the immediate environment of the massive crystalline rock is required for Si, Fe, K, Mg, Ca, and Al, in order to account for the observed secondary minerals. While Mg, K, and Ca are indigenous to seawater, Si, Fe, and Al were probably enriched in the fluid during wall rock reactions in the fracture system.It is suggested that diagenesis of layer 2 basalts results in the extraction of Mg and K from seawater, in enough quantity to contribute significantly to the chemical mass balance of the oceans.     

Silicon K-edge XANES spectra of silicate minerals

Silicon K-edge x-ray absorption near-edge structure (XANES) spectra of a selection of silicate and aluminosilicate minerals have been measured using synchrotron radiation (SR). The spectra are qualitatively interpreted based on MO calculation of the tetrahedral SiO ₄ ^4? cluster. The Si K-edge generally shifts to higher energy with increased polymerization of silicates by about 1.3 eV, but with considerable overlap for silicates of different polymerization types. The substitution of Al for Si shifts the Si K-edge to lower energy. The chemical shift of Si K-edge is also sensitive to cations in more distant atom shells; for example, the Si K-edge shifts to lower energy with the substitution of Al for Mg in octahedral sites. The shifts of the Si K-edge show weak correlation with average Si-O bond distance (d_Si-O), Si-O bond valence (s_Si-O) and distortion of SiO₄ tetrahedra, due to the crystal structure complexity of silicate minerals and multiple factors effecting the x-ray absorption processes.     

黑云母的红外光谱研究

关于云母族矿物的红外光谱研究,国内外一些学者曾做过不少工作。笔者就近年来所收集到的一些产自宁芜地区、南岭地区花岗岩类岩石中27个黑云母样品,进行了红外光谱测定,确定了某些特征吸收峰的偏移及其与化学组分之间的关系,并探讨了黑云母矿物中主要金属阳离子的相互置换和     

Compositional variation within some glauconites and illites and implications for their stability and origins

Textural, mineralogical and chemical data are presented for glauconites and illites from the Lower Cretaceous Glauconitic Sand Formation, Alberta, Canada. Single crystal analyses by scanning transmission electron microscopy (STEM) indicate that both glauconite (29 analyses) and illite (44 analyses) correspond very closely to ideal dioctahedral structures. Al dominates the octahedral sheet in illite. Very extensive A1 for Fe^III substitution was also found in some of the glauconites, much more than previously recorded. The dioctahedral mica structure is clearly very stable and flexible with respect to A1 for Fe^III substitution. Iron-poor glauconites were found associated with pyrite. We believe that glauconites tend to lose iron progressively during burial diagenesis, especially where pore water iron activities are low (high HS^? activity and low Eh). It seems probable that A1 for Si tetrahedral substitution also takes place during diagenesis with consequent loss of swelling properties. This is the same trend which is responsible for conversion of smectite to illite. Glauconite forms only where sediments reside for lengthy periods at the interface between oxidizing and reducing environments, where Fe³⁺ is transiently available in solution. Related marine and terrestrial nontronites also form only in similar ‘interface’ environments.     

西太平洋海山玄武岩的岩石学特征及与上覆富钴结壳的关系

通过对西太平洋海山玄武岩和玄武质火山角砾岩的岩石学特征及其气孔充填物成分变化的研究,讨论了海山玄武岩与上覆富钴结壳的关系。富钴结壳的基岩火山岩主要为碱性玄武岩和玄武质火山角砾岩。碱性玄武岩中气孔充填物为S型和C型,S型和C型气孔充填物不共存在同一个气孔中。S型气孔充填物的物质成分富Si、Fe、K、Mg、Al,Co含量一般为0.17%~0.46%,其成分与碱性玄武岩的组成类似,其物质来源可能与碱性玄武岩有关。C型气孔充填物为O、Ca、C及少量Si、Al、Mg、Fe、K等元素,C型气孔充填物可能与海水中物质的沉积有关。由Si、Al、Fe、Mg、K等元素变化曲线反映出的S型气孔充填物沉积过程与富钴结壳早期的沉积过程具有相似的趋势,说明富钴结壳早期沉积物的物质来源可能与碱性玄武岩有关,富钴结壳物质来源可能是碱性玄武岩和海水共同作用的结果。     

焦家式金矿中铬铝云母化学成分的标型性

本文系统研究了胶东地区金矿中产出的铬铝云母亚族中３个白云母、１６个绢云母和３２个含Ｃｒ云母种属的化学成分特征。提出了含Ｃｒ云母种属结构层内四面体、八面体及层间离子种类和数量在焦家式金矿成矿过程中的指示作用，阐明了白云母、绢云母及含Ｃｒ云母种属之间的演化特征在与焦家式金矿化有关的成岩成矿作用中的标型意义。     

辽河盆地西部凹陷粘土矿物的成岩作用研究

对辽河盆地西部凹陷兴隆台、马圈子、欢喜岭和曙光等地沙河街组不同深度的层位,高升地区(属弱碱性和弱氧化-弱还原环境的沙四段分别采样,经X-光衍射、电子显微镜、化学分析和差热、红外等项目的分析鉴定,研究区内的粘土矿物有: 蒙脱石 在全区较浅的地层(如欢喜岭地区小于1000米,兴隆台地区小于1500米)中均有分布。其主要成份为二八面体的钙蒙脱石。 皂石 为黑色橄榄-辉石玄武岩的次生产物。     

Crystal Chemistry Research of Minerals of Nigerite Group and Its Significance

SinceJacobsonandWebb (194 7)firstlyfoundthenigeriteinNigeria ,mineralogistshavefounditinmanycountriessuchasRussia (EastSiberia ,195 8) ,China(Hunan ,196 3) ,Portugal (196 5 ) ,Australia (1976 )andsoon .Greyetal.(1979)determinedaccuratelythecrystalstructureofnigerite (2 4R) .In 1988,Chenfoundakindofendmembermineralofnigerite ,whichisMg riched .ByapprovingofCommissiononNewMineralsandMineralNames (CNMMN) ,thismineralwasnamedpengzhizhongite .Inthepast ,somemineralogistsdidnotfurtherdis t…     

古盐度对塔北隆起泥岩中粘土矿物组合和绿泥石成分的影响

粘土矿物组合和绿泥石成分常被用来讨论盆地沉积物的成岩作用和埋藏古温度。许多沉积盆地的研究结果显示,泥 岩和页岩中的粘土矿物组合和绿泥石的成分与埋藏深度/温度有关。但也见有例外的现象存在。文中主要探讨了新疆塔北隆 起泥岩中的粘土矿物组合和绿泥石成分的特征,以及与盆地古盐度的关系。研究结果表明：（1）在塔北隆起泥岩中,埋藏 深度2777.37~4604.41m,地层单位为J1-N2的粘土矿物组合为I+Chl和I+Chl+Ka; 埋藏深度5071.52~5299.37m,地层单位为 T1的粘土矿物组合为R0I/S+I+Chl和R0I/S+Chl。（2）研究区的成岩绿泥石为Ⅱb型铁镁绿泥石,其成分特征主要表现为： ①配位八面体中阳离子的占位数为11.532(总平均值);②ⅥAl含量明显大于ⅣAl含量;③（Fe+Mg）为4.016（总平均值）;④ Si/Al比值>1。（3）根据研究区盐类矿物的分布范围以及古盐度的数据,讨论了古盐度对该区粘土矿物组合和绿泥石成分的 影响,指出古盐度是影响本区粘土矿物组合和绿泥石成分变化的主要因素。用古盐度解释了<5000m深度的粘土矿物组合 中不含无序伊/蒙混层（R0I/S）矿物,而>5000m深度粘土矿物组合中含有无序伊/蒙混层（R0I/S）矿物的异常现象。揭示了 在一定的深度范围（2777.37~4405.27m）,一定的古盐度条件下（Sr/Ba比值≥0.4,并有盐类矿物出现）,绿泥石成分受到 古盐度的制约,并且随着古盐度的增高,绿泥石成分中的Al、ⅣAl、Na、Na2O、Al/Si随之增高,而Si/Al则随之降低。由 绿泥石成分温度计获得的温度值也伴随着古盐度的增高而增高。因此,由绿泥石成分温度计所计算的温度不能代表本区实 际埋藏的古温度。（4）研究区内绿泥石成分中的SiO2和FeO与母岩的对应成分之间有一定的相关性,其SiO2绿泥石与SiO2岩石、 FeO绿泥石与FeO岩石呈负相关的线性关系,并且这种关系在古盐度的干扰下也未受到影响。