凹凸石粘土与玄武岩的成因关系

在矿物组成研究的基础上，对比研究了凹凸棒石，蒙脱石，凹凸棒石粘土，蒙脱石粘土，玄武岩，风化玄武岩的化学组成。根据化学成分对比，分析了玄武岩与凹凸棒石粘土的成因关系，解释了玄武岩对凹凸棒石粘土的时空控制，结合地质观测，提出形成苏皖地区凹凸棒石粘土的物质成分基本上来源于玄岩的化学风化，但物质成分发生了较大的分异，凹凸棒石粘土不能直接同玄武岩经地表雨水的风化淋滤形成，而是玄武岩风化形成的蒙脱石经搬运沉积，再与镁质溶液反应形成，或凹凸棒石直接从富镁碱性溶液中结晶形成，凹凸棒石粘土形成的物理化学条件为偏碱性的还原条件。     

The smectite–chlorite transition in drillhole NJ-15, Nesjavellir geothermal field, Iceland: XRD, BSE and electron microprobe investigations

Abstract In well NJ-15 of the Nesjavellir geothermal field, Iceland, the transition of discrete smectite into discrete chlorite has been studied from drill cuttings recovered at depths of less than 1714 m and over a continuous range of temperatures between 60 and 300° C. At temperatures below 180° C, the clay fractions contain mixtures of di- and trioctahedral smectites, whose layer charge increases with depth. Between 200 and 240° C, discrete smectites have transformed into smectite-rich, randomly interstratified chlorite and smecite ( R 0 C/S). Because the abundance of chlorite interlayers in this C/S is generally <20%, its presence can be detected only by electron microprobe techniques and not by X-ray diffraction. Between 245 and 265° C, both regularly ( R 1) and randomly interstratified C/S are the predominant layer silicates. Discrete chlorite first appears at approximately 270° C and coexists with minor amounts of R 0 C/S at higher temperatures.
R 0 and R 1 C/S form a nearly complete compositional series between trioctahedral saponite and discrete chlorite end-members. The interlayer cation and Si content of smectites and C/S decrease with increasing temperature. The Mg/(Mg + Fe) content of smectite, C/S, and chlorite is unrelated to temperature. The percentage of chlorite in C/S, as determined by electron microprobe analyses, increases continuously with increasing temperature, except for occurrences of smectite-rich C/S in fresh basaltic dykes which have not thermally equilibrated with the higher grade country rocks.     

Regional retrograde alteration of sub-greenschist facies chlorite to smectite

Dioctahedral smectite is present as a retrograde alteration product of chlorite in Permian-Triassic red slates of the Malaguide Complex in Sierra de Espuña (Betic Cordillera). Mineral assemblages and textures, illite crystallinity indices, and fluid inclusion data indicate sub-greenschist facies conditions that reached at least 180°C in the higher-grade tectonic unit of the Malaguide Complex, preceding formation of smectite. Smectite, having K as the dominant interlayer cation, occurs ubiquitously intercalated with trioctahedral chlorite as thin packets of layers and as individual layers that commonly change to chlorite along layers. Although some chlorite is typically homogeneous and trioctahedral, much chlorite shows signs of alteration and has compositions corresponding to different degrees of smectite contaimination. The incompatibility of metamorphic grade with the occurrence of smectite, the general association of chlorite and smectite, and the textural relations collectively show that dioctahedral smectite is derived through replacement of trioctahedral chlorite. Such replacement occurs on a regional basis and demonstrates that caution must be used in interpreting the occurrence of smectite in pelites as being due to prograde processes. Alteration of trioctahedral chlorite under oxidizing conditions due to introduction of phreatic water after uplift of the Betic Cordillera is proposed as the cause of formation of smectite.     

Clay petrology of the Upper Triassic/Lower Jurassic terrestrial strata of the Newark Supergroup,Connecticut Valley,U.S.A.

The clay mineralogy of the Newark Supergroup (Upper Triassic/Lower Jurassic) in the Connecticut Valley was studied by X-ray diffraction analysis. Clay minerals identified in 126 samples are illite, chlorite, smectite, kaolinite, vermiculite, expandable chlorite, mixed-layer illite/smectite, mixed-layer chlorite/smectite, and mixed-layer chlorite/vermiculite. In general, the rocks are illitic with subordinate amounts of chlorite. However, the various lithofacies in the Newark Supergroup are characterized by distinct clay-mineral assemblages. Red beds of floodplain origin contain clays mainly of detrital nature with 2M illite most abundant. Subordinate amounts of chlorite, smectite, vermiculite, kaolinite and mixed-layer illite/smectite are also present. An interstratified chlorite/vermiculite occurs in red mudstone underlying basalt flows. Lacustrine gray beds are generally characterized by the clay-mineral assemblage 1Md illite + chlorite with minor amounts of smectite ane expandable chlorite. An interstratified chlorite/smectite predominates in gray mudstone associated with perennial lake cycles in the East Berlin Formation. Black shales of deeper lacustrine origin contain the assemblage 1Md ifillite + trioctahedral smectite and traces of chlorite. Illite and smectite also occur as mixed-layer phases.In many respects, the distribution of clay minerals in the Connecticut Valley can be likened to the general scheme proposed for the Permo-Triassic basins of Europe and Africa. These display both vertical and horizontal variations in clay-mineral assemblages that reflect the chemical and spatiotemporal evolution of intrabasin depositional and diagenetic environments. Chemical data indicate that magnesium, especially, was concentrated in the black muds of large perennial lakes that intermittently occupied the Connecticut rift valley. Pore waters derived from these sediments played an important role in the development of Mg-rich 2 : 1 and interstratified clay minerals during early diagenesis.     

Clay minerals in sediments of the hydrothermally active southern trough in the Guaymas Basin (Gulf of California)

The results of the study of clay mineral alterations in Upper Pleistocene sediments of the southern trough in the Guaymas Basin (Gulf of California) due to the influence of hydrothermal solutions and heat produced by sill intrusions are discussed. Core samples from DSDP Holes 477 and 477A were taken for the analysis of clay minerals. Application of the method of modeling X-ray diffraction patterns of oriented specimens of the finely dispersed particles made it possible to establish the phase composition of clay minerals, determine their structural parameters, and obtain reliable quantitative estimates of their contents in natural mixtures. The modeling data allowed us to characterize reliably the transformation of clay minerals in sediments of the hydrothermally active southern trough in the Guaymas Basin. In Upper Pleistocene sandy–clayey sediments of the southern trough, changes in the composition of clay minerals occurred under the influence of a long-living hydrothermal system. Its lower part (interval 170.0–257.5 m) with maximum temperatures (~300°C) was marked by the formation of chlorite. Terrigenous clay minerals are not preserved here. Saponite appears at a depth of 248 m in the chlorite formation zone. Higher in the sedimentary section, the interval 146–170 m is also barren of terrigenous clay minerals. Sediments of this interval yielded two newly formed clay minerals (chlorite and illite), which were formed at lower temperatures (above 180°C and below 300°C, approximately up to ~250°C), while the relatively low-temperature upper part (110–146 m) of the hydrothermal system (from ~140°C to ~180°C) includes the mixture of terrigenous and newly formed clay minerals. Terrigenous illite is preserved here. Illitization of the mixed-layer illite–smectite was subjected to illitization. The terrigenous montmorillonite disappeared, and chlorite–smectite with 5–10% of smectite layers were formed. In the upper interval (down to approximately 110 mbsf), the composition of terrigenous clay minerals remains unchanged. They are composed of the predominant mixed-layer illite–smectite and montmorillonite, the subordinate illite, mixed-layer chlorite–smectite with 5% of smectite layers, mixed-layer kaolinite–smectite with 30% of smectite layers, and kaolinite. This composition of clay minerals changed under the influence of sill intrusions into the sedimentary cover at 58–105 m in the section of Hole 477. The most significant changes are noted in the 8-m-thick member above the sill at 50–58 m. The upper part of this interval is barren of the terrigenous mixed-layer illite–smectite, which is replaced by the newly formed trioctahedral smectite (saponite). At the same time, the terrigenous dioctahedral smectite (montmorillonite) is preserved. The composition of terrigenous clay minerals remains unchanged at the top of the unit underlying the sill base.     

Microstructures and compositional variation in the intravolcanic bole clays from the eastern Deccan volcanic province: Palaeoenvironmental implications and duration of volcanism

Clay minerals associated with intra-volcanic bole horizons of varied colours and thicknesses contain montmorillonite, halloysite and kaolinite, show distinct microstructures and microaggregates. In kaolinite, Fe³⁺ ions substitute for Al³⁺ at octahedral sites. Most of these clays are dioctahedral type, show balance between net layer and interlayer charges. The interstratified illite — smectite (I/S) mixed layers containing variable proportions of montmorillonite. Illite contains sheet-like, well oriented microaggregates. The parallel stacks of chlorite sheets show chlorite/smectite (C/S) mixed layers. Progressive enrichment of Fe and depletion of Al ions with the advancement of kaolinization process is observed. High order of structural and compositional maturity observed in these bole clays, indicate long hiatus between the two volcanic episodes.     

Origin of fibrous clays in Tunisian Paleogene continental deposits

This paper presents mineralogical and geochemical data from several continental sequences located in Central (Ain Ghréwiss and Kébar) and Central-Southern Tunisia (Selja, Kef Schefeir, Shib, Oum El Kcheb and Haidoudi). These sequences vary in age from Late Palaeocene to Early Oligocene and contain considerable quantities of fibrous clays (up to 75% palygorskite and 90% sepiolite). These clays appear in assocation with carbonates (mainly dolomite), detrital aluminosilicates (illite, Al smectites, mixed-layers illite–smectite and kaolinite), quartz and lesser quantities of gypsum and halite. The textural characteristics observed by electron microscopy, the trace and rare earth elements contents and their distribution in the various mineral phases, together with the isotopic composition of dolomite and fibrous clays, provide good clues as to the genesis of the neoformed minerals. Thus, the sepiolite would have precipitated directly in lacustrine, playa-lake or sebka environments under alkaline conditions, high Si and Mg and low Al activity, and arid to semiarid climate. On the other hand, the palygorskite would have formed by transformation of already existing illite and/or smectite type aluminosilicates in solutions in equilibrium with isotopically heavier and, therefore, more evaporated solutions than the sepiolite.     

Petrography and provenance of the Early Permian Fluvial Warchha Sandstone,Salt Range,Pakistan

The Warchha Sandstone of the Salt Range of Pakistan is a continental succession that accumulated as part of a meandering, fluvial system during Early Permian times. Several fining-upward depositional cycles are developed, each of which is composed of conglomerate, cross-bedded sandstone and, in their upper parts, bioturbated siltstone and claystone units with distinctive desiccation cracks and carbonate concretions. Clast lithologies are mainly of plutonic and low-grade metamorphic origin, with an additional minor sedimentary component. Textural properties of the sandstone are fine- to coarse-grained, poorly to moderately sorted, sub-angular to sub-rounded, and with generally loose packing. Based on modal analyses, the sandstone is dominantly a feldspathoquartzose (arkose to sub-arkose). Detrital constituents are mainly composed of monocrystalline quartz, feldspars (more K-feldspar than plagioclase) and various types of lithic clasts. XRD and SEM studies indicate that kaolinite is the dominant clay mineral and that it occurs as both allogenic and authigenic forms. However, illite, illite-smectite mixed layer, smectite and chlorite are also recognised in both pores and fractures. Much of the kaolinite was likely derived by the severe chemical weathering of previously deposited basement rocks under the influence of a hot and humid climate. Transported residual clays deposited as part of the matrix of the Warchha Sandstone show coherent links with the sandstone petrofacies, thereby indicating the same likely origin. Illite, smectite and chlorite mainly occur as detrital minerals and as alteration products of weathered acidic igneous and metamorphic rocks. Based primarily on fabric relationship, the sequence of cement formation in the Warchha Sandstone is clay (generally kaolinite), iron oxide, calcareous and siliceous material, before iron-rich illite and occasional mixed layer smectite–illite and rare chlorite. Both petrographic analysis and field characteristics of the sandstone indicate that the source areas were characterised by uplift of a moderate to high relief continental block that was weathered under the influence of hot and humid climatic conditions. The rocks weathered from the source areas included primary granites and gneisses, together with metamorphic basement rocks and minor amounts of sedimentary rocks. Regional palaeogeographic reconstructions indicate that much of the Warchha Sandstone detritus was derived from the Aravalli and Malani ranges and surrounding areas of the Indian Craton to the south and southeast, before being transported to and deposited within the Salt Range region under the influence of a semi-arid to arid climatic regime.     

Retrograde alterations of phyllosilicates in low-grade metapelite: a case study from the Szendr? Paleozoic, NE-Hungary

Frequently, at temperatures lower than the metamorphic peak conditions, slates undergo mineral transformations, usually mediated by fluids. We have studied core material of an epizonal slate series (Szendr? Mountains, NE-Hungary) to reconstruct the post-metamorphic lower-T hydrothermal alterations using petrographic, X-ray diffraction, electron microprobe methods, and transmission electron microscopy. The borehole crosscuts an upper part of the ca. 600?C800?m Lower-Carboniferous flysch-like Szendr? Phyllite Formation. The samples were metamorphosed reaching epizonal conditions with a mineral assemblage characterized by quartz, muscovite, chlorite and albite. Even in the freshest samples, break-up and loosening of the regional metamorphic structure was observed, with cracks parallel to or crossing the cleavage. In the upper part, chlorite and albite are almost absent, while the presence of paragonite, mixed Na?CK mica, and mixed-layered minerals with smectitic component are characteristic. Goethite, halloysite, and subordinate kaolinite are present in the most altered sample (13.0?m in the profile) which may indicate the position of the fissures in which the circulation of the post-metamorphic fluids was the most intense. Muscovite is the only mica from the lower part of the profile and chlorite becomes a significant constituent, whereas paragonite, halloysite, and kaolinite are missing. Discrete smectite is present in all the samples in spite of being incompatible with the prograde evolution of the sequence. The interleaved smectite layers in chlorite and muscovite/chlorite mixed-layers show at the lattice level textural characteristics indicative of a later alteration process. After the metamorphic peak at epizonal conditions, the introduction of hot fluids through the fractures gave rise to the crystallization of Na?CK white micas and muscovite/chlorite under anchizonal conditions. In a final stage of the hydrothermal process, the cooling of the circulating fluids favored the formation of halloysite and kaolinite in the areas near to the fissures, smectites in the samples far away from the fractures, and locally, goethite. The Fe₂O₃ content increasing upwards indicates oxidizing conditions in the late stage of hydrothermal activity and/or eventually, an influence of a younger near-surface weathering.     

SEDIMENTS FROM BAY ST. GEORGE, NEWFOUNDLAND

Sediments cored to a depth of about 1 m in Bay St. George, Newfoundland, were examined for grain-size distribution and minerals. The sediments are light brown silty clays, the principal minerals of which are chlorite and muscovite mica. The scarce sand consists of fresh detrital grains of blue-green amphibole, biotite, epidote, zoisite, magnetite, garnet, hypersthene, apatite, chlorite, and scarce zircon. Quartz, plagioclase feldspar, and muscovite are abundant. These minerals are all present in the rocks of the adjacent land areas and have been deposited in the sediments with little alteration or change due to weathering. The clay minerals of the sediments are predominantly muscovite and chlorite with a slight admixture of vermiculite and montmorillonite. There is very little mixed-layering of these minerals. Montmorillonite may be due to diagenetic changes after deposition of these clays in the marine environment of the bay.     

Evaluation of redox-active iron sites in smectites using middle and near infrared spectroscopy

Redox processes of structural Fe in clay minerals play an important role in biogeochemical cycles and for the dynamics of contaminant transformation in soils and aquifers. Reactions of Fe(II)/Fe(III) in clay minerals depend on a variety of mineralogical and environmental factors, which make the assessment of Fe redox reactivity challenging. Here, we use middle and near infrared (IR) spectroscopy to identify reactive structural Fe(II) arrangements in four smectites that differ in total Fe content, octahedral cationic composition, location of the negative excess charge, and configuration of octahedral hydroxyl groups. Additionally, we investigated the mineral properties responsible for the reversibility of structural alterations during Fe reduction and re-oxidation. For Wyoming montmorillonite (SWy-2), a smectite of low structural Fe content (2.8 wt%), we identified octahedral AlFe(II)-OH as the only reactive Fe(II) species, while high structural Fe content (>12 wt%) was prerequisite for the formation of multiple Fe(II)-entities (dioctahedral AlFe(II)-OH, MgFe(II)-OH, Fe(II)Fe(II)-OH, and trioctahedral Fe(II)Fe(II)Fe(II)-OH) in iron-rich smectites Ölberg montmorillonite, and ferruginous smectite (SWa-1), as well as in synthetic nontronite. Depending on the overall cationic composition and the location of excess charge, different reactive Fe(II) species formed during Fe reduction in iron-rich smectites, including tetrahedral Fe(II) groups in synthetic nontronite. Trioctahedral Fe(II) domains were found in tetrahedrally charged ferruginous smectite and synthetic nontronite in their reduced state while these Fe(II) entities were absent in Ölberg montmorillonite, which exhibits an octahedral layer charge. Fe(III) reduction in iron-rich smectites was accompanied by intense dehydroxylation and structural rearrangements, which were only partially reversible through re-oxidation. Re-oxidation of Wyoming montmorillonite, in contrast, restored the original mineral structure. Fe(II) oxidation experiments with nitroaromatic compounds as reactive probes were used to link our spectroscopic evidence to the apparent reactivity of structural Fe(II) in a generalized kinetic model, which takes into account the presence of Fe(II) entities of distinctly different reactivity as well as the dynamics of Fe(II) rearrangements.     

The smectite to chlorite transition in a fossil seamount hydrothermal system: the Basement Complex of La Palma, Canary Islands

Abstract The hydrothermal metamorphism of a sequence of Pliocene-aged seamount extrusive and volcanoclastic rocks on La Palma includes a relatively complete low-P-T facies series encompassing the zeolite, prehnite-pumpellyite, and greenschist facies. The observed mineral zonations imply metamorphic gradients of 200–300° C km^-1. The transition from smectite to chlorite in the La Palma seamount series is characterized by discontinuous steps between discrete smectite, corrensite and chlorite, which occur ubiquitously as vesicles and, to a much lesser extent, vein in-fillings. Trioctahedral smectites [(Mg/(Fe + Mg) = 0.4–0.75] occur with palagonite and Na-Ca zeolites such as analcime and a thompsonite/natrolite solid solution. Corrensite [(Mg/(Fe + Mg) = 0.5–0.65] first appears at stratigraphic depths closely corresponding to the disappearance of analcime and first appearance of pumpellyite. Discrete chlorite [(Mg/(Fe + Mg) = 0.4–0.6] becomes the dominant layer silicate mineral coincident with the appearance of epidote and andraditic garnet. Within the stratigraphic section there is some overlap in the distribution of the three discrete layer silicate phases, although random interstratifications of these phases have not been observed. Although smectite occurs as both low- and high-charge forms, the La Palma corrensite is a compositionally restricted, 1:1 mixture of low-charge, trioctahedral smectite and chlorite. Electron microprobe analyses of coarse-grained corrensite yield structural formulae close to ideal values based on 50 negative charge recalculations. Calcium (average 0.20 cations/formula unit) is the dominant interlayer cation, with lesser Mg, K and Na. The absence of randomly interlayered chlorite/smectite in the La Palma seamount series may reflect high, time-integrated fluid fluxes through the seamount sequence. This is consistent with the ubiquity of high-variance metamorphic mineral assemblages and the general absence of relict igneous minerals in these samples.     

Clay Minerals in Basalt Sills from the Sediment Cover,East Pacific Rise

Clay minerals in basalt sills from the northern East Pacific Rise, covered by Upper Pleistocene clayey–sandy–silty sediments (turbidites, hemipelagites, and diatom oozes) sampled from DSDP Holes 477, 478, and 481A, were studied by X-ray methods based on the modeling of diffraction patterns. Trioctahedral smectites formed in thin (0.1–0.5 and 1.8–4 m) fissured sills that are well permeable for water delivered from the water-saturated host sediments heated by the sills. Smectites in basalts are found in the interstices (20–40 vol % in the rock and up to 50–80 vol % in hyalobasalts). They replace olivine and fill cracks and vesicles. Plagioclase and clinopyroxene are generally unaltered. The structure of smectites is characterized by different height of layers depending on the composition of cations in the interlayers and the degree of their hydration. The different-height layers either make up individual smectite phases or alternate in different proportions and with a high degree of segregation in the mixed-layer structures. Under conditions of a prolonged cooling, thick (43 m) sills are distinguished from the thin varieties by the formation of trioctahedral minerals (smectite–chlorite, chlorite, defective chlorite, and talc). They are found mainly in the interstices that make up 3–7 vol % of the rock.     

Evidences of felsic volcanism and hydrothermal activities from clays associated with the Palaeoproterozoic Porcellanite Formation of the Vindhyan Supergroup,Central India

Chemico-mineralogical attributes of authigenic clays associated with the altered volcanic tuffs that occur in the Palaeoproterozoic Porcellanite Formation contain evidences of hydrothermal alteration and diagenetic processes in a marine environment. Previous sedimentological and geochemical studies on Porcellanite Formation were restricted to the Chopan area, but, the details related to provenance, nature and source of volcanism archived in these clays have not been ascertained. In order to understand these aspects, present study on these authigenic clays were carried out. Clay minerals represent dominance of illite with subordinate amount of montmorillonite. Moreover, low abundance of kaolinite is also noticed. The illite fibers and plates associated with the kaolinite indicate illitization. The kaolinite to illite transformation is favoured by incorporation of K⁺ ions, derived from the K-feldspar dissolution and its overgrowth. Major oxide contents of these clays and their ratios when plotted over diagrams marked with standard illite, kaolinite, smectite and chlorite compositional fields show clustering within or close to the illite field. Thermodynamic components calculated for these clays when plotted over AR₂³⁺AlSi₃O₁₀(OH)₂ − R₂³⁺Si₄O₁₀(OH)₂ − AR²⁺R³⁺Si₄O₁₀(OH)₂ ternary diagram, data plots lie within the illite, mixed layer I/S and smectite fields. Binary major oxide data plots between bulk rock and authigenic clay compositions showed felsic affinity. Montmorillonite and illite predominated in the eastern and western marginal areas of the Vindhyan Basin, respectively. However, former resulted from the hydrothermal alteration of volcanic glass associated with the ferruginous breccia and altered tuffs and remnants of the volcanic vents, whereas, later is associated with the tuffaceous beds. Owing to the adsorption, Ba, Rb and Sr is enriched in clays comparing to the bulk rock composition. Low (< 15 ppm) Sc values suggested major contribution from the felsic component. Also, low Rb/Sr and Th/U values revealed moderate insitu weathering. The dominance of K-feldspar alteration and insitu weathering is also evident from clustering of clay data plots in the A-CN-K ternary diagram. Pronounced negative Eu anomaly together with higher LREE/HREE values associated with these clay minerals implied proximity to source and their possible derivation from the silicified felsic tuffs available in the provenance.     

Formation of corrensite, chlorite and chlorite-mica stacks by replacement of detrital biotite in low-grade pelitic rocks

Transmission and scanning electron microscopy were utilized to investigate the nature and mechanisms of alteration of abundant detrital biotite of volcanic origin and progressive modification of phyllosilicate aggregates in a prograde sequence of pelitic rocks (illite crystallinity index = 0.19–0.58λ2θ) from the Gaspé Peninsula in Quebec.
Detrital biotite has been diagenetically altered to form corrensite and chlorite through two mechanisms; (1) layer-by-layer replacement gave rise to interstratification of packets of layers and complex mixed layering via several kinds of layer transitions between biotite and chlorite, corrensite or smectite; (2) dissolution-transport-precipitation resulted in the formation of relatively coarse-grained aggregates of randomly orientated, corrensite-rich flakes and fine-grained corrensite intergrown with chlorite and illite in the matrix.
The data show that stacks consisting of alternating packets of trioctahedral and dioctahedral phyllosilicates originated during early diagenesis when lenticular fissures in strained altering biotite were filled by dioctahedral clays. Subsequent prograde evolution of dioctahedral clays occurred through deformation, dissolution and crystallization, and overgrowth. Illite evolved to muscovite, with K in part provided through biotite alteration, and corrensite/chlorite to homogeneous chlorite. The alteration of detrital biotite is closely related to the formation of titanite and magnetite in diagenetic rocks, and pyrite, calcite and anatase or rutile in the higher grade rocks.
The observations demonstrate that detrital biotite of volcanic origin may be the principal precursor of chlorite in chlorite-rich metapelites originating in marginal basins. The mineral parageneses suggest that the transitions from corrensite to chlorite and illite to muscovite may be a function of local chemistry and time.     

安徽官山两种坡缕石粘土的成分与红外吸收谱

本文采用多种成分分析手段对官山两种不同颜色坡缕石全粘土进行了研究。全粘土湿化学分析扣除SiO2含量计算得到的坡缕石阳离子数与电子探针获得的阳离子数一致。配位八面体阳离子计算表明，粉红色坡缕石为三八面体矿物，灰白色坡缕石是介于三八面体矿物和二八面体矿物间的中间类型。X射线粉末衍射的K值法对全粘土矿物定量分析有着较高的精度，同时用电子探针波谱可准确测定坡缕石粘土的成分。官山两种不同颜色含坡缕石的全粘土红外吸收谱能反映其中坡缕石的吸收谱特征。对X射线光电子能谱研究表明两种不同颜色的坡缕石中的铁主要是Fe^3 ，这与全岩湿化学分析的结果是一致的，同时也还可以作为电子探针成分分析的补充。     

中国含油气盆地粘土矿物的某些矿物学特征

本文总结归纳了２０多个含油气盆地粘土矿物的类型，讨论了８种较常见的、６种较少见的和３种极少见的粘土矿物的Ｘ射线衍射特征及其成分、形态和分布等方面的矿物学特征．     

Palygorskite from cave sediments: case study from Wadi Haqil,United Arab Emirates

The x-ray powder diffraction identification of clay minerals both in bulk samples and in separated clay fraction confirmed the presence of palygorskite in samples of cave sediments from Wadi Haqil (the western slopes of Musandam Mountains; Ras Al-Khaimah Emirate, UAE). Samples contain quartz, gypsum, smectite, kaolinite, calcite, and palygorskite, some of them chlorite, illite, feldspars, and goethite. Calcite dominates in most samples; smectite prevails in clay fraction. After heating, the 001 reflection of chlorite shifts to higher diffraction angles and its intensity decreases; these features indicate that the chlorite represent a Fe-dominant species. Unit-cell dimensions of major phases as refined by the Rietveld method are in agreement with literature data. Chemical composition of palygorskite was derived from unit-cell dimensions as follows: MgO content is 11–14 wt% and Al₂O₃ 10–13 wt%. Clay mineralogy is only hard to ascertain from the scanning electron microscope (SEM) images even after being combined with the energy-dispersive spectrometer data. The SEM was also used to characterize gypsum grains; they often display flow deformation features. Studied cave sediments represent palygorskite-bearing weathering products and desert soils re-deposited from the cave surroundings by slope processes and wind and/or surface runoff. The mixture with other clay minerals, quartz, feldspars, etc. supports this interpretation. Fine-grained quartz fraction is probably wind-blown. Gypsum and calcite are the precipitates (crusts and/or cements), although gypsum can also be re-deposited from omnipresent gypsum-cemented surface sediments.     

青海循化盆地晚渐新世沉积物中坡缕石的特征及其古气候指示意义

采用X射线衍射和扫描电子分析方法,对青海循化盆地晚渐新世沉积物的矿物组成、坡缕石的矿物学特征以及古气候指示作用进行了深入的研究。结果表明,晚渐新世循化盆地沉积物中粘土矿物组成主要有蒙脱石、伊利石、坡缕石和绿泥石等;坡缕石一般呈纤维状或者针状,沿片状蒙脱石的边缘及表面交代生长,为典型自生成因的坡缕石。坡缕石是干旱-半干旱气候条件的特征矿物,其出现表明循化地区晚渐新世气候特征较为干旱,与粘土矿物组合及伊利石结晶度所反映的气候环境信息相吻合;沉积物中坡缕石相对含量及有序度自下而上逐渐增大,说明循化地区的干旱化逐渐加剧。循化地区晚渐新世(～23 Ma)的干旱化可能与青藏高原隆升或者全球气候变冷事件密切相关。     

Multi-stage zeolite facies mineralization in the Hvalfjördur area,Iceland

The Hvalfjördur area, 30 km north of Iceland’s capital Reykjavik, belongs to the sequence of Late Tertiary to early Quaternary flood basalts with minor intercalations of hyaloclastites and rhyolites. The basalts are affected by progressive low-temperature metamorphism, caused by the burial of the lava succession and higher heat flow from nearby central volcanoes. Low-grade zeolite facies metamorphism of basaltic lavas in the Hvalfjördur area results in two distinct mineral parageneses that can be correlated to events in the burial and hydrothermal history of the lava pile. Stage Ia represents syn-eruptive near-surface alteration in which celadonite and silica were precipitated along primary pores. During regional burial metamorphism (stage Ib), hydrolysis of olivine and glass led to the formation of mixed-layer chlorite/smectite clays. The chlorite content of stage Ib phyllosilicate vesicle rims increases with increasing burial depth and temperature. Stage II occurred after the burial and is marked by zeolite mineralization caused by higher heat flow from the Laxárvogur and Hvalfjördur central volcanoes. Altogether 11 different zeolites were found in the Hvalfjördur area: analcime, chabazite, epistilbite, heulandite, laumontite, levyne, mesolite, stilbite, stellerite, thomsonite and yugawaralite. In total, three separate depth and temperature-controlled “zeolite zones” occur in the Hvalfjördur area.