Mineralogy and chemical composition of the clay fraction of Neogene shales from the Surma Group in the Bengal basin,Bangladesh

Mineralogical and chemical investigations (<2μm clay separates) of shale samples from the Neogene-age Surma Group obtained from four wells (Habiganj-11, Shahbazpur-1, Titas-11, Titas-15) in the Bengal basin, Bangladesh, were carried out in order to reveal the clay mineral composition as reservoir exploration and exploitation requires a good understanding of the clay minerals. The samples were analyzed by X-ray diffraction (XRD), scanning electron microscope (SEM) and X-Ray fluorescence spectrometry (XRF). Mineralogically, the sub-surface Surma Group shales comprise predominantly quartz, plagioclase, illite, chlorite, kaolinite, with lesser amounts of K-feldspar, dolomite and smectite, and minor to trace amounts of calcite, siderite and pyrite. The chemical composition of the <2 μm clay separates also suggests an illite and chlorite-rich composition. With increasing burial depth, the Surma Group shales are enriched in illite. The gradual decreasing of the smectite clays with depth and ultimate disappearance at greater depths (≥ 3000 m) may have been responsible for the presence of the diagenetic illite. Based on the mineralogical composition it is most likely that the illite-chlorite associations together with quartz and feldspar were predominantly detrital in origin and thus reflect the presence of a rapidly-rising source terrain not subjected to intense weathering.     

Quantitative analysis of the clay minerals in the Shurijeh Reservoir Formation using combined X-ray analytical techniques

The Shurijeh Reservoir Formation of Neocomian age is represented by a sandstone sequence, occasionally interbedded with shale, in the Gonbadli gas field, Kopet-Dagh Basin, Northeastern Iran. In this study X-ray diffraction (XRD) and X-ray fluorescence (XRF) techniques were used together to characterize the Shuirjeh clay minerals in 76 core samples collected from two deep Gonbadli wells. The results of XRF analysis showed high percentages of silicon and moderate to low percentages of aluminum, sulfur, calcium, potassium, sodium, magnesium, and iron in both wells. The XRD analysis indicated that the above elements were concentrated in the form of quartz, anhydrite, dolomite, calcite, plagioclase, K-feldspar, hematite, and clay minerals. Further XRD examination of the clay fraction revealed that illite, chlorite, and kaolinite were the major types of clay minerals. Unlike, glauconite, smectite, and a mixed layer clays of both the illite–smectite and chlorite–smectite types were observed only in very few samples. The percentages of individual clay minerals were determined using external standard calibration curves and successfully validated by a system of simultaneous linear equations acquired from detailed elemental information based on the XRF analysis. The error reached ± 5% for the main mineral constituent and ± 15% for minor minerals. A local regression relationship was also derived, based on the XRF elemental information, which can be used to estimate the clay contents of other Shurijeh drilled wells with data of pulsed-neutron spectroscopy tools. According to the proposed quantitative approach, the amount of illite varied considerably, reaching 18.3%. In contrast, the amounts of kaolinite and chlorite were generally small, i.e., less than 8.4%. The amount of total clay minerals changed greatly from a minimum of 5% to a maximum of 32.5%. An increase in illite with increasing burial depth and temperature was an obvious indication of deep burial diagenesis in this formation.     

A New Discovery of the Cretaceous/Tertiary Boundary from the Tethyan Belt,Hekimhan Basin,Turkey: Mineralogical and Geochemical Evidence

A Cretaceous/Tertiary (K/T) boundary location within the Tethyan region (present Mediterranean area) has been discovered in the Hekimhan basin, Malatya, Turkey. The K/T transition in a 1.65-m-thick marine evaporitic facies (gypsum and celestite) consists of laminated carbonate rocks (limestone, dolomitic limestone, dolomite) and marl in the upper part, and laminated limestone and marl in the lower part. The K/T boundary is marked by a 6-mm-thick clay layer that is entirely greenish pink in color. The stratum is characterized by a decrease in calcite content, and by an increase in the proportion of smectites and K-feldspar. Palygorskite and rarely serpentine are associated with smectite. A minimum in CaO + MgO content exists at the K/T boundary. The amounts of some transition metals, miscellaneous, low- and high-field-strength, platinum-group, and rare-earth elements reveal a substantial anomaly at the K/T boundary that supports both terrestrial (volcanic) and extraterrestrial (bolide) hypotheses.     

A new simple approach to evaluate pedogenic clay transformation in a Vertic Calcisol

The aim of this study is to characterize the pedogenic clay minerals by using simple approach: mixing mineralogical and geochemical findings.The fine clay fractions (< 0.1 μm) of a Vertic Cambisol profile were studied by means of X-ray diffraction (XRD), infrared spectroscopy (FTIR) and cation exchange capacity (CEC).Qualitative and quantitative mineralogical compositions of the clay mixture were determined.Moreover, chemical equilibria and thermodynamic stabilities of minerals (calcite, gypsum, kaolinite, smectites and illites) were studied using results of ionic activities obtained from total concentration of various aqueous species in water extracts from soil-saturated pastes.XRD analysis shows a good homogeneity in the mineralogical composition of the soil material, with depth of soil profiles. The identified clay minerals are mainly illite–smectite mixed layers (I/S) and kaolinite. The chemical analysis of saturated paste extracts with clay minerals shows a slight undersaturation of the illitic phase while smectites and also calcite and gypsum reach the thermodynamic equilibrium along the soil profile.     

Mechanisms of siderophore sorption to smectite and siderophore-enhanced release of structural Fe

Sorption of the trihydroxamate siderophores desferrioxamine-B and -D (DFOB and DFOD, respectively) and of the monohydroxamate ligand acetohydroxamic acid (aHA) to smectite were examined in batch sorption studies (pH 5.5, 0.1 M ionic strength) coupled with X-ray diffraction (XRD) and Fourier transform infrared (FTIR) spectroscopy. Both DFOB and DFOD, which have similar molecular structures but different charge properties (cationic versus neutral, respectively) showed a high affinity for smectite. In contrast, the smaller aHA molecule did not sorb appreciably. XRD analysis indicated that DFOB and DFOD each absorbed in the interlamellar region of the clay to give d-spacings of 13.4-13.7 Å at equilibrium solution concentrations <250 μM. FTIR spectra of sorbed DFOB and DFOD indicated that the conformation of each species was distinct from its conformation in the crystalline or dissolved states. At elevated initial solution concentrations of 500-1500 μM, DFOB formed a bilayer in the clay interlayer. Changes in the FTIR spectra of the DFOB-loaded clay samples at these higher surface loadings were consistent with the presence of a metal-siderophore complex in the interlayer. DFOB and DFOD both enhanced Fe and Al release from smectite, but aHA did not. Possible dissolution mechanisms are discussed in light of the FTIR and batch dissolution results.     

Iron Speciation of Mud Breccia from the Dushanzi Mud Volcano in the Xinjiang Uygur Autonomous Region, NW China

Organic-inorganic interactions occurring in petroleum-related mud volcanoes can help predict the chemical processes that are responsible for methane emissions to the atmosphere. Seven samples of mud breccia directly ejected from one crater were collected in the Dushanzi mud volcano, along with one argillite sample of the original reddish host rocks distal from the crater, for comparison purposes. The mineral and chemical compositions as well as iron species of all samples were determined using XRD, XRF and M?ssbauer spectroscopy, respectively. The results indicate that a series of marked reactions occurred in the mud volcano systems, more specifically in the mud breccia when compared to the original rocks. Changes mainly included: (1) some conversion of clay minerals from smectite into chlorite and illite, and the precipitation of secondary carbonate minerals such as calcite and siderite; (2) silicon depletion and significant elemental enrichment of iron, manganese, magnesium, calcium and phosphorus; and (3) transformation of iron from ferric species in hematite and smectite into ferrous species in siderite, chlorite and illite. These geochemical reactions likely induced the color changes of the original reddish Neogene argillite to the gray or black mud breccia, as a result of reduction of elements and/or alteration of minerals associated with the oxidation of hydrocarbons. Our results also suggest that greenhouse gases emitted from the mud volcanoes are lowered through a series of methane oxidation reactions and carbon fixation (i.e., through carbonate precipitation).     

Geochemical assessment of Paleocene limestones of Sinn El-Kaddab Plateau,South Western Desert of Egypt,for industrial uses

The present work assesses the potential industrial uses of Paleocene limestone deposits, Garra Formation in Sinn El-Kaddab Plateau, South Western Desert of Egypt, based on their mineralogy and geochemical characteristics. Eighty-six limestone samples collected from ten stratigraphic columnar sections were analyzed using X-ray diffraction (XRD) and X-ray fluorescence (XRF) techniques. Petrographically, Garra limestone deposits consist dominantly of benthic foraminiferal wackestone and packstone microfacies. The XRD data revealed dominance of low-Mg calcite as essential carbonate mineral in the studied limestone. The bulk rock XRF results revealed CaO (29.28–55.75%) with an average of 52.74%. The CaO exhibits a strong negative correlation with MgO, SiO₂, TiO₂, Al₂O₃, and moderate negative correlation with Fe₂O₃ which indicates that the contribution of these elements is mainly due to detrital input. On the other hand, Al₂O₃ and Na₂O contents exhibit significant negative correlation with loss of ignition (LOI) wt% indicating their incorporation within terrigenous matrix. The average Sr content attains 1297 ppm indicating deposition in temperate marine environment. The average molar CaCO₃% values of bulk samples have been computed for individual columnar sections to determine the purity status of Garra limestone deposits. They range from impure (CaCO₃%?=?79.92%) to high-pure (CaCO₃%?=?97.76%) limestone. Therefore, Garra limestone deposits have extremely valuable uses in a wide spectrum of industrial applications including Portland cement, steel, ceramics, whiting, chemical uses, paper, and feed stuff.     

Rock composition and origin of the Duwi Formation calcareous rocks, Upper Egypt

Upper Cretaceous phosphorite beds of the Duwi Formation, Upper Egypt, are intercalated with limestone, sandy limestone, marl, calcareous shales, and calcareous sandstone. Calcareous intercalations were subjected to field and detailed petrographic, mineralogical and geochemical investigations in order to constrain their rock composition and origin. Mineralogically, dolomite, calcite, quartz, francolite and feldspars are the non-clay minerals. Smectite, kaolinite and illite represent the clay minerals. Major and trace elements can be classified as the detrital and carbonate fractions based on their sources. The detrital fraction includes the elements that are derived from detrital sources, mainly clay minerals and quartz, such as Si, Al, Fe, Ti, K, Ba, V, Ni, Co, Cr, Zn, Cu, Zr, and Mo. The carbonate fraction includes the elements that are derived from carbonates, maily calcite and dolomite, such as Ca, Mg and Sr. Dolomite occurs as being dense, uniform, mosaic, very fine-to-fine, non-ferroan, and non-stoichiometrical, suggesting its early diagenetic formation in a near-shore oxidizing shallow marine environment. The close association and positive correlation between dolomite and smectite indicates the role of clay minerals in the formation of dolomite as a source of Mg^2＋ -rich solutions. Calcareous rocks were deposited in marine, oxidizing and weakly alkaline conditions, marking a semi-arid climatic period. The calcareous/argillaceous alternations are due to oscillations in clay/carbonate ratio.     

Mineralogy of Holocene Sediments from the Southwestern Black Sea Shelf (Turkey) in Relation to Provenance, Sea-level and Current Regimes

Grain size and mineral composition of core sediments were used to investigate influences of various terrestrial and marine conditions, which have prevailed on the southwestern Black Sea shelf during the Holocene. Siliciclastic mud with small amounts of sand and gravel from nearby coastal hinterland is the principal sediment type, whereas sediments deposited near the shelf edge and the Istanbul Strait and off the Duru Lake （a paleo-river mouth） constitued large quantities of sand and gravel of both biogenic and terrigenic origin. Variable amounts of aragonite, 1 nmmicas, quartz, feldspars, calcite and dolomite constitute the dominant non-clay minerals in bulk sediments. The clay mineral assemblage in the 〈 2 μm fraction is made up of smectite, illite, kaolinite and chlorite. Aragonite and calcite are mainly derived from benthic accumulations, whereas feldspars （mainly plagioclase） and smectite reflect magmaticvolcanic provenance and the distribution of 1 nm-micas and chlorite correlate with nearby metamorphic sources onland. Nevertheless, grain size and mineral distribution generally indicate a combination of effects of wind and wave climate, longshore and offshore cyclonic currents, changing sea-level stands and nearby source rock and morphological conditions. It is also suggested that at least part of clay minerals could be derived from the northwesterly Danube River input.     

黄骅坳陷三马地区中-深部储层成岩作用及主控因素分析

黄骅坳陷三马地区储集岩样品的显微特征及成岩矿物的组合关系分析结果表明，三马地区下第三系中深层储层主要处于晚成岩A期，成岩现象包括石英、长石的次生加大、碳酸盐矿物胶结作用、矿物交代作用、溶解作用和粘土矿物转化作用等。其中石英次生加大于2700m左右开始出现，随埋深增大，石英增生加强；长石次生加大现象不十分普遍；碳酸盐胶结作用包括早期自生泥晶方解石胶结作用、连晶方解石和晚期白云石(或铁方解石)的胶结作用。在扫描电镜下可见到方解石与含铁方解石集合体充填在粒间孔隙中或与石英、钠长石及粘土矿物共生，白云岩多呈菱形粒状分布于粒间；常见的交代现象主要有方解石交代长石、石英及粘土矿物，粘土矿物交代长石、石英等；溶解作用主要有长石的溶解、碳酸盐颗粒的溶解和方解石胶结物的溶解等，粘土矿物的转化主要为蒙脱石、高岭石向伊利石(或绿泥石)转化。还讨论了储层岩相、岩性特征、孔隙水中有机酸含量、早期方解石的充填、烃类早期注入等因素对储层成岩演化的控制作用。     

兰州市取暖期可吸入颗粒物中单颗粒矿物组成特征

为研究兰州市2005年冬季大气可吸入颗粒物(PM10)中单颗粒的矿物组成,用能谱扫描电镜识别和统计了兰州市区(东方红广场)和郊区(榆中县)两个采样点的单矿物颗粒。结果在市区样品中识别出方解石、伊/蒙混层、石英、斜长石、伊利石、石膏、绿泥石、高岭石、浊沸石和钾长石等21种矿物,前7种占统计总量的75%以上;郊区样品中识别出20种矿物,以方解石、石英、伊利石、绿泥石、斜长石和伊/蒙混层为主(占70%以上),与市区相比缺少钾石膏、金红石和水铝酸钙而增加了硫酸镁和磷灰石。总体来看,大气PM10中的矿物颗粒可分为粘土类、长石类、碳酸盐类、硫酸盐类、氧化物类和其他六类,以粘土类和碳酸盐类矿物为主(约占60%);冬季市区颗粒物表面的“硫化”现象较郊区严重;这些矿物颗粒主要来自地表土,人为排放和大气中二次化学反应生成的矿物的贡献较小。     

River water quality in weathered limestone: A case study in upper Mahanadi basin, India

Stromatolitic limestone and calcareous shale belonging to Chattisgarh Supergroup of Proterozoic age dominate the upper part of the Mahanadi river basin. X-ray diffractogram (XRD) of limestone rocks show presence of a significant amount of calcite, dolomite and ankerite. Shales of various colours contain calcite and dolomite. It is observed that congruent dissolution of carbonate minerals in the Charmuria pure limestone has given rise to a typical karst topography. On the other hand, limestones are also seen to support red and black soil profiles. This indicates that the limestone bedrock undergoes a parallel incongruent weathering, which leaves a residue of decomposed rock. The XRD analyses reveal that the limestone soils thus formed contain an assemblage of quartz, clays and Fe-oxides. It is likely that the silicate component trapped during deposition of the stromatolitic limestone weathers incongruently resulting in diverse soil profiles. Carbonate and silicate mineral weathering schemes have been worked out to explain the soil formation, fixation of Al in clay minerals, and Fe in goethite. The water quality parameters such as Ca, Mg and HCO₃ in the river water suggest under saturation with respect to calcite and dolomite. The mineral stability diagrams indicate that kaolinite and Ca-smectite are stable in the river water environment, hence they occur in suspended sediments and soils. The dominant influence of carbonate weathering on the water quality is observed even in the downstream part of the river outside the limestone terrain.     

Textural evidences for dissolution of silica-rich rocks of the Ypresian phosphatic series,Gafsa-Metlaoui basin,southwestern Tunisia: implication of biogenic silica supply on genesis of fibrous clays

The present work aimed to determine the mineralogical composition of Ypresian series and to clarify the influence of the dissolution of siliceous frustules on the genesis of fibrous clay minerals. The specimens sampled from CPG trench are mainly constituted of silica-rich rocks at Mides area located at the western part of Gafsa-Metlaoui basin. The samples were investigated using X-ray diffraction (XRD) and scanning electron microscopy (SEM) in order to determine texture of constituents. The data obtained indicate that the bulk rock samples are mainly made up of opal CT and clay minerals. The latter consists of palygorskite-sepiolite minerals associated with smectite and few amount of illite. The trend of mineralogical composition indicates that fibrous clay minerals are more concentrated at the upper part. SEM observations indicated that palygorskite mineral appears as thread-like facies, which surround foliated texture of smectite in the lower part of the Mides section, although with the low Mg activity confirmed by the absence of dolomite. But, at the upper part of the Mides section, SEM observations revealed the occurrence of siliceous frustules, which have numerous dissolved areas and replacement of carbonate tests by silica. The dissolution saturated the depositional environment with silica which is required for the formation of palygorskite and sepiolite minerals, in addition to high Mg activity confirmed by the presence of dolomite in the bulk rock, which is required basically for the formation of sepiolite. Although the genesis mode of palygorskite and sepiolite is similar with very little difference, the genesis of sepiolite needs a high alkalinity than the formation of palygorskite.     

Analcime in lake and lake-margin sediments of the Carboniferous Rocky Brook Formation, Western Newfoundland, Canada

In the Deer Lake Basin of western Newfoundland, Canada, analcime has been found within fine-grained, siliciclastic and carbonate, lake and lake-margin sediments of the Carboniferous Rocky Brook Formation. Analcime is the only zeolite observed in these unmetamorphosed and non-volcanogenic rocks. Microscopic analcime occurs as vug-filling, limpid, isotropic to anisotropic crystals. Microprobe analyses show this type of analcime to be lower in silica than most analcime in sedimentary rocks. A second textural type of finer-grained submicroscopic analcime can be detected from X-ray diffraction spectra of Rocky Brook Formation mudstones, where it is associated with phyllosilicates (illite, interstratified chlorite/smectite, smectite, chlorite), other silicates (quartz, feldspar) and carbonates (dolomite, calcite). Results of this study suggest that the analcime in the Rocky Brook Formation formed either by direct lakewater/porewater precipitation or by reaction of these waters with one or more clay mineral types or plagioclase.     

Stratigraphic status,age, and paleobathymetry of the Grey shale Member,Dalmiapuram Formation,Cauvery Basin,India

Grey shale Member of the Dalmiapuram Formation, Ariyalur Group, Cauvery Basin, India was studied for its stratigraphic position, age, and paleobathymetry with a re-look into the lithological relationship and foraminifer assemblages in the deepened limestone mine excavations at M/s Dalmia Cements, Dalmiapuram. Twenty grey shale samples from Kovandankurchchi (pit-4) and Kallakkudi mines yielded diversified calcareous, benthic, and rare index planktic foraminifera. The foraminiferal assemblages suggest a latest Albian age and middle neritic depositional conditions. The abundance of kaolinite and smectite clay minerals relate to warm/humid climate which corroborate with rising relative sea level during grey shale deposition. The grey shale occurs in patches within the marl bedded limestone member which exhibits cyclic deposition of limestone and marl. The limestone mine sections demonstrate that the grey shale forms part of basal marl bedded limestone, directly overlying the coral algal limestone. The present study demonstrates that the grey shale outcrops in Dalmiapuram Formation should be placed stratigraphically as part of marl bedded limestone. The member status for grey shale which is current usage stands discounted.     

Adsorption of copper and zinc onto natural clay in single and binary systems

Calcareous and smectitic clay samples from the Coniacian–Lower Campanian system, Tunisia, were used as adsorbents for the removal of copper and zinc from aqueous solutions in single and binary systems. Calcareous clay sample was treated with acetic acid to obtain carbonate-free sample that was also used for metals removal. The adsorption of metal ions onto natural clay was tested in a batch method by mixing 1 g/L of each sample with a metal ion solution of zinc (300 μmol/L) and/or copper 600 μmol/L under the operating pH of 6, and agitation speed of 200 rpm within the equilibrium time of 60 min at 25 °C for single and binary systems. Our results showed that natural clay samples were mainly composed of silica, alumina, iron, and magnesium oxides. Adsorption data showed that the studied clay samples removed substantial amounts of heavy metals in single and mixed systems. Initial solution pH and carbonates contents enhanced the removal capacities of the studied clay samples, confirming their strong influencing effects. Thermodynamic parameters indicated an endothermic adsorption for metals removal by calcareous clay, but exothermic process for the smectitic sample. These results suggest that the Late Cretaceous clays, Tunisia, can be effectively used as natural adsorbents for the removal of toxic heavy metals in aqueous systems.     

Reflectance spectroscopy and geochemical analyses of Lake Hoare sediments, Antarctica: implications for remote sensing of the Earth and Mars

Visible to infrared reflectance spectroscopic analyses (0.3-25 micromoles) have been performed on sediments from the Dry Valleys region of Antarctica. Sample characterization for these sediments includes extensive geochemical analyses and X-ray diffraction (XRD). The reflectance spectra and XRD indicate major amounts of quartz, feldspar, and pyroxene in these samples and lesser amounts of carbonate, mica, chlorite, amphibole, illite, smectite, and organic matter. Calcite is the primary form of carbonate present in these Lake Hoare sediments based on the elemental abundances and spectroscopic features. The particle size distribution of the major and secondary components influences their detection in mixtures and this sensitivity to particle size is manifested differently in the "volume scattering" and "surface scattering" infrared regions. The Christiansen feature lies between these two spectral regimes and is influenced by the spectral properties of both regions. For these mixtures the Christiansen feature was found to be dependent on physical parameters, such as particle size and sample texture, as well as the mineralogy. Semiquantitative spectroscopic detection of calcite and organic material has been tested in these quartz- and feldspar-rich sediments. The relative spectral band depths due to organics and calcite correlate in general with the wt% C from organic matter and carbonate. The amounts of organic matter and carbonate present correlate with high Br and U abundances and high Ca and Sr abundances, respectively. Variation in the elemental abundances was overall minimal, which is consistent with a common sedimentary origin for the forty-two samples studied here from Lake Hoare.     

Geochemistry,Petrography and Spectroscopy of Organic Matter of Clay‐Associated Kerogen of Ypresian Series: Gafsa‐Metlaoui Phosphatic Basin,Tunisia

This work presents geochemical characterization of isolated kerogen out of clay fraction using petrography studies, infrared absorption and solid state ¹³C nuclear magnetic resonance (NMR) spectroscopy, with N‐alkane distributions of saturated hydrocarbon. Mineralogical study of clay mineral associations was carried out using X‐ray diffraction (XRD), on Ypresian phosphatic series from Gafsa‐Metlaoui basin, Tunisia. The XRD data indicate that smectite, palygorskite and sepiolite are the prevalent clay minerals in the selected samples. In this clay mineral association, the N‐alkane (m/z = 57) distribution indicates that the marine organic matter is plankton and bacterial in origin. The kerogens observed on transmitted light microscopy, however, appear to be totally amorphous organic matter, without any appearance of biological form. The orange gel‐like amorphous organic matter with distinct edges and homogenous texture is consistent with a high degree of aliphaticity. This material has relatively intense CH₂ and CH₃ infrared bands in ¹³C NMR peaks. This aliphatic character is related to bacterial origin. Brown amorphous organic matter with diffuse edges has a lower aliphatic character than the previous kerogen, deduced from relatively low CH₂ and CH₃ infrared and ¹³C NMR band intensities.     

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.     

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.