Sediments within accretionary complexes, preserving key information on crust growth history of Central Asian Orogenic Belt, did not get enough attention previously. Here, we conduct comprehensive geochemical study on the turbidites from the North Tianshan Accretionary Complex (NTAC) in the Chinese West Tianshan orogen, which is a good example of sediments derived from juvenile materials. The turbidites, composed of sandstone, siltstone, and argillaceous siliceous rocks, are mainly Carboniferous. All the investigated samples have relatively low Chemical Index of Alteration values (35–63) and Plagioclase Index of Alteration values (34–68), indicating relatively weak weathering before erosion and deposition. The sandstone and siltstone, and slate samples display high Index of Compositional Variability values of 0.89–1.50 and 0.89–0.93, suggesting a relatively immature source. The sandstones and siltstones were mainly derived from intermediate igneous rocks, and the slates from felsic igneous rocks, formed in oceanic/continental arc settings. The investigated samples roughly display high positive εNd(t) values (mainly at +5.5 to +7.9, except one spot at +0.8), with corresponding Nd model ages at 672 Ma–522 Ma (except one at ∼1.1 Ga). Combined with the previous studies, we suggest that the turbidites in the NTAC were mainly derived from intermediate to felsic igneous rocks with juvenile arc signature, and thus the northern Chinese West Tianshan is a typical site with significant Phanerozoic crust growth.

In situ elemental imaging of planetary surface regolith at a spatial resolution of 100s to 1000s of microns can provide evidence of the provenance of rocks or sediments and their habitability, and can identify post-depositional diagenetic alteration affecting preservation. We use high-resolution elemental maps and XRF spectra from MapX, a flight prototype in situ X-ray imaging instrument, to demonstrate this technology in rock types relevant to astrobiology. Examples are given for various petrologies and depositional/diagenetic environments, including ultramafic/mafic rocks, serpentinites, hydrothermal carbonates, evaporites, stromatolitic cherts and diagenetic concretions.

Stylistic shifts in ceramics are often linked with sociopolitical changes, yet adopting new ceramic designs may indicate anything from shared aesthetic appeal to emulation. Focusing on multiple ceramic technologies is critical for understanding ceramic changes as they relate to wider social fluctuations. The relationships between clay and ceramic recipes, and communities of practice, have not been studied at the urban landscape of Angamuco, Michoacán in western Mexico. Petrographic and geochemical analyses of tempers and fabrics indicate that ceramics, including imperial Purépecha (a.d. 1350–1530) vessels, were created from local and regional materials, and that these materials remained relatively stable for over 1,000 years. Ceramic archaeometry in western Mexico has been relatively limited compared to other parts of Mesoamerica, and this study may be compared to future studies in the region.

The mineralogy and geochemistry of shales reflect the composition of the initially deposited precursor mud, subsequently modified by diagenetic processes. To see if significant geochemical differences exist between shales that mainly owe their present-day composition to either deposition or diagenesis, we compare the published mineralogical, bulk and clay-fraction geochemical, and clay-fraction O-isotopic compositions of 2 shales. One shale is from the Western Canada Sedimentary Basin (WCSB), and its composition mainly reflects primary (depositional) chemical and mineralogical variations (smectitic to illitic illite/smectite) within this unit. The other shale is from the United States Gulf Coast (USGC), and its composition mainly reflects mixed-layer illite/smectite (I/S) diagenesis of deposited smectitic clay material. The chemical and mineralogical trends of WCSB and USGC shales, including one of increasing illite content in I/S with depth or maturity, are essentially indistinguishable, in both bulk shale and clay fraction, despite the contrasting genetic interpretations for the origin of the contained I/S. Thus, similar mineralogical and chemical trends with depth or temperature can result either from inherited depositional compositional heterogeneity of the sediment, from burial metamorphism of shale or a combination of both. Interestingly, the O-isotopic compositions of the clay fractions from the WCSB and USGC are significantly different, a fact that reflects original clay formation from source material and water of quite different isotopic compositions. The discrimination between depositional and diagenetic contributions to shale composition continues to pose challenges, but a combination of bentonite, illite polytype, clay isotopic and trace and rare earth elemental analyses together with illite age analysis holds promise for future work.

Upper Cretaceous-Tertiary marine clayey-calcareous rocks of the Hekimhan basin contain fibrous clay minerals in significant amounts. Ophiolitic rocks in the provenance area have contributed the elements to form the clay minerals. XRD, SEM, major, trace and REE analyses were applied to samples taken from several stratigraphic sections. Diagenetic minerals such as smectite, dolomite, calcite, gypsum, celestite and quartz/chalcedony are associated with sepiolite-palygorskite group clays. Trace and rare earth elements (REE) are more abundant in palygorskite than sepiolite. REE abundances in the sepiolite-palygorskite are characterized by negative Eu and positive Nd anomalies when normalized with respect to chondrite and shale. Sepiolites with sharp XRD peaks are formed by diagenetic replacement of dolomite and diagenetic transformation of palygorskite, or by direct crystallization from solution. The average structural formula of the sepiolite is:

(Mg7.15Al0.13Fe0.31Cr0.06Ni0.04)(Si11.98Al0.02)O30(OH)4(OH2)4Ca0.03Na0.02K0.02.8H2O

Palygorskite appears to be authigenic by direct precipitation from solution. It exists in both monoclinic and orthorhombic forms with the mean structural formula given below

(Mg2.22Al1.00Ti0.04Fe0.77Cr0.01Ni0.02)(Si7.68Al0.32)O20(OH)2(OH2)4Ca0.07Na0.05K0.10.4H2O

Large-scale geological structures have controlled the long-term development of the bed and thus the flow of the West Antarctic Ice Sheet (WAIS). However, complete ice cover has obscured the age and exact positions of faults and geological boundaries beneath Thwaites Glacier and Pine Island Glacier, two major WAIS outlets in the Amundsen Sea sector. Here, we characterize the only rock outcrop between these two glaciers, which was exposed by the retreat of slow-flowing coastal ice in the early 2010s to form the new Sif Island. The island comprises granite, zircon U-Pb dated to ~177–174 Ma and characterized by initial ɛNd, 87Sr/86Sr and ɛHf isotope compositions of -2.3, 0.7061 and -1.3, respectively. These characteristics resemble Thurston Island/Antarctic Peninsula crustal block rocks, strongly suggesting that the Sif Island granite belongs to this province and placing the crustal block's boundary with the Marie Byrd Land province under Thwaites Glacier or its eastern shear margin. Low-temperature thermochronological data reveal that the granite underwent rapid cooling following emplacement, rapidly cooled again at ~100–90 Ma and then remained close to the Earth's surface until present. These data help date vertical displacement across the major tectonic structure beneath Pine Island Glacier to the Late Cretaceous.

The widespread Balıkesir bentonite deposits within the Miocene volcano-sedimentary units in western Anatolia have economic potential; they are important raw materials for the paper and bleaching industries in Turkey. No detailed geological, mineralogical, geochemical, or genesis characterizations of these bentonite deposits have been carried out to date. The present study was undertaken to close this gap. The mineralogical characteristics of the bentonites and their parent rocks were examined using polarized-light microscopy, X-ray powder diffractometry (XRD), scanning- and transmission-electron microscopies (SEM–EDX and TEM), and chemical (ICP–AES and –MS) methods. In the bentonite deposits, smectite is associated with smaller amounts of illite, chlorite, quartz, feldspar, dolomite, calcite, opal-CT, and amphibole. The smectite was identified by sharp basal reflections at 14.42–14.93 Å. Plagioclase and sanidine crystals in volcanic units are altered and sericitized. Biotite and hornblende are partly to completely Fe-(oxyhydr)oxidized and chloritized. Smectite flakes occur on altered feldspar and mica grains and devitrified volcanic glass fragments in association with or without calcite ± dolomite crystals. Increasing Al+Fe+Mg/Si ratios with increasing degree of alteration reveal that hydration of volcanogenic grains (feldspar, mica, hornblende, glass shard) favored precipitation of smectite with montmorillonite composition, with an average structural formula: (Ca0.31Na0.05K0.08)(Al2.72Fe0.17Mg1.27Ti0.011Mn0.01)(Si7.94Al0.06)O20(OH)4. The concentration of Al2O3 and MgO and increase of LREE/HREE ratio, and a distinct, negative Eu anomaly show that smectite was probably formed as a result of the decomposition of volcanic feldspar, mica, amphibole, and volcanic glass. Association of carbonate rocks within the smectite-rich material and the absence of chlorite and detrital materials such as rock fragments in the bentonites suggest that the bentonite deposits formed authigenetically as ‘primary bentonites’ from volcanoclastic materials deposited in a calm lacustrine–palustrine environment during an early diagenetic process.

The varied mineralogical composition of earthy materials and the quantity of elements extracted by simulated stomach acid substantiate the diversity of materials consumed by humans practicing geophagy. Direct consumption of ‘edible earths’ for medicinal and spiritual purposes occurs worldwide and is deeply rooted in ‘folk medicine’ and religion. The legends associated with the healing powers of the clay from Chimayo, New Mexico, provide an excellent example of the roots of geophagy. The clay mineral assemblages revealed by X-ray diffraction analysis of 22 samples from New Mexico, North America, and other parts of the world are highly variable. One might be monominerallic kaolinite or smectite, and another, a complex mixture of illite, kaolinite, smectite, and chlorite or vermiculite. The quantities of elements (Al, Si, K, Na, Ca, Mg, Fe, Mn, Ti, P, S, Ba, Sr, Pb, Zn, Cd, Co, Cu, Cr, Ni, V, Zr, Se, Mo, Be, Sb, and As) extracted by 0.12 M HCl varied from ∼1.0 mg/g to the limit of detectability, 0.0001 mg/g. Potential long-term human health effects were evaluated with the Reference Dose Ratio (RDR). It divides the quantity of the element extracted from 50 g of the total sample by the recommended reference dose (RfD) reported in the Environmental Protection Agency’s (EPA, USA) IRIS (Integrated Risk Information System) database. Median RDR values for Na, Cr, Sb, and As exceeded 1.0 indicating an abnormally high potential intake. Materials consumed by humans are so varied that caution should be used in comparing the results of one clay study with those of another without mineralogical and chemical data.

Widespread alteration in the Upper Cretaceous pyroclastic units of the Tirebolu (Giresun) area, NE Turkey, has resulted in significant occurrences of bentonite with economic potential. No detailed geological, mineralogical, or geochemical characterization of these occurrences has been carried out to date. The aim of this study was to describe the geological background, the mineralogical, chemical, and stable-isotope characteristics of the bentonite, and major aspects of their formation, e.g. type and source of low-temperature alteration, mass balance, chemical evolution of the smectites, and geochemistry of major and trace elements. The bentonite contains abundant smectite with occasional kaolinite and mordenite, volcanogenic feldspar, quartz, biotite, hornblende, glass shards, and pumice fragments, along with the diagenetic minerals, opal-CT, and, in some locations, calcite. X-ray diffraction patterns of the clay fractions exhibit characteristics of pure montmorillonite and beidellite-type smectite. Micromorphologically, the smectite exhibits a honeycomb texture, the kaolinite occurs in both vermiform and irregular platy forms, and the mordenite occurs in fibrous form. All of these minerals are edged with devitrified volcanic glass and resorbed feldspar. Chemically, the smectites are Ca-smectite. Geochemical data indicate that alteration of the pyroclastic units took place under suboxic and anoxic environmental conditions during bentonite formation. Field observations and mineralogical, geochemical, oxygen, and hydrogen isotopic data indicate that the alteration of feldspar and volcanic glass in the pyroclastics by mixed meteoric and sea water in a shallow marine environment under alkaline and acidic conditions, respectively, controlled by environmental Al, Ca, and Na concentrations, resulted in the formation of authigenic smectite, mordenite, and kaolinite. A large Ca content in the smectite originated from surrounding units, which resulted in high alkalinity; Mg originated from seawater.

A field-mapping and crystal-chemical study of two alunite- and halloysite-rich deposits in the Turplu area, situated northwest of Balıkesir on the Biga Peninsula of northwest Turkey reveals a mineralogically diverse and a potentially economic clay deposit. The mineral assemblage along fault zones is dominated by halloysite and sometimes alunite. The alunite is nearly end-member in composition (a = 6.995 Å, c = 17.195 Å) often occurring with a minor Ca phosphate phase. Of the two deposits studied, the more northerly mine contains more alunite relative to halloysite. Geochemical alteration indices suggest that the northern mine has experienced a slightly greater degree of hydrothermal modification. Halloysite is found in both hydrated and dehydrated states and assumes a tubular morphology. Observations by transmission and scanning electron microscopy are consistent with a model of halloysite dehydration, where the shapes transform from an open-hole tubular morphology to a closed-hole unfurled morphology.

Mineral paragenesis includes the effects of initial deposition of volcanic tuffs and andesite on top of karstic terrain. The contact between altered volcanics and underlying limestones is irregular and appears to have provided a mechanism to flush both hydrothermal and meteoric waters through the volcanics. Periods of hydrothermal alteration (hypogene) contemporaneous with extensional and strike-slip faulting have resulted in alunite and halloysite deposits. Hydrothermal alteration is concentrated near the fault zones. Because of subsequent weathering (supergene) away from the fault zones, much of the andesitic volcanic rocks have been altered to a more smectite-rich and kaolinite-bearing assemblage. The deposits continue to be both plastically deformed in the alunite/halloysite regions and to undergo brittle deformation in the saprolitized volcanics. Tectonic deformation has mixed the contacts, such that limestone blocks are entrained into parts of the alteration zones. Gibbsite and gypsum are common weathering products associated with limestone block inclusions. Genetic models for the origins of alunite-halloysite deposits in NW Turkey should consider as possible influencing factors the underlying lithologies, the extent of hydrothermal alteration, and recent weathering by meteoric fluids. In the case of the Turplu deposits, karstic limestones, hydrothermal circulation of sulfate-rich waters, and a post-alteration history of meteoric weathering were all important factors in their formation.

The Kütahya kaolinite deposits are the most important source of raw materials for the ceramics industry in Turkey. To date, no detailed mineralogical or geochemical characterizations of these materials have been carried out; the present study aims to fill that gap. The Kütahya kaolinite deposits formed by alteration of dacite and andesite tuffs related to Neogene volcanism whichwas associated withe xtensional tectonics. The kaolinite deposits contain silica and Fe- and Ti-bearing phases (pyrite, goethite, and rutile) in vertical and subvertical veins that diminish and then disappear upward. Mineralogical zonation outward from the main kaolinite deposit is as follows: kaolinite ± smectite + illite + opal-CT + feldspar; feldspar + kaolinite + quartz + smectite + illite; quartz + feldspar + volcanic glass. The veins and mineral distributions demonstrate that hydrothermal alteration was the main process in the development of the kaolinite deposits of the area. The very sharp, intense, diagnostic basal reflections at 7.2 and 3.57 Å, as well as non-basal reflections, well defined pseudohexagonal to hexagonal crystallinity with regular outlines, ideal differential thermal analysis-thermal gravimetric curves, and ideal, sharp, infrared spectral bands indicate well crystallized kaolinite. Micromorphologically, the development of kaolinite plates at the edges of altered feldspar and devitrified volcanic glass indicates an authigenic origin. Lateral increase in (SiO2+Fe2O3+MgO+Na2O+CaO+K2O)/(Al2O3+TiO2) from the center of the kaolinite deposit outward also indicates hydrothermal zonation. Enrichment of Sr in altered and partially altered rocks relative to freshvolca nic-rock samples demonstrates retention of Sr and depletion of Rb, Ba, Ca, and K during hydrothermal alteration of sanidine and plagioclase within the volcanic units. In addition, depletion of heavy rare earth elements (HREE) relative to light rare earth elements (LREE) in the kaolinized materials may be attributed to the alteration of hornblende. The negative Eu anomaly suggests the alteration of feldspar by hydrothermal fluids. The isotopic data from kaolinite and smectite indicate that hydrothermalalteration processes developed at 119.1–186.9°C and 61.8–84.5°C, respectively. Thus, the kaolinite deposits formed by hydrothermal alteration of volcanic glass, feldspar, and hornblende by a dissolutionprecipitation mechanism which operated under acidic conditions within Neogene dacite, andesite, and tuffs.

Hydrous Al-silicate deposits are found to the south of Pütürge in Malatya city, Turkey. The surrounding rocks consist of mylonitic granitic gneiss overlain by muscovite gneiss with kyanite-bearing metabasic schist lenses on top which are cut by silica veins containing prismatic tourmaline and speculante. Pyrophyllite is found within kyanite gneisses overlying the granitic gneisses. Fibrous, platy pyrophyllite is developed along the edges and cleavage planes of kyanite, whereas platy bunches of dickite occur as replacements of the relict kyanites as well as crack- and pore-fillings. Rocks forming the hydrous Al-silicate deposit contain 2M1 pyrophyllite, alunite, topaz, paragonite, dravite, dumortierite, chlorite and epidote as early hypogene minerals, and 2M1 dickite, diaspore, gibbsite, speculante, goethite and crandallite/goyazite as late hypogene minerals. On the basis of fluid inclusion and stable isotope data, it is estimated alterations to pyrophyllite and kaolinite occurred at temperatures are of 150 and 100°C, respectively, the minerals being formed by meteoric waters interacting with metamorphic rocks. Trace and REE variations are highly distinctive in terms of enrichment of most trace elements in pyrophyllite, whereas REEs are clearly abundant in dickite, indicating different conditions during formation such as early and late hypogene processes. The pyrophyllitic alteration took place in the late Cretaceous (69–71 Ma), whereas kaolinization occurred later.

A detailed stratigraphic and facies reconstruction of a bentonitized acid-tuff succession, deposited within the transgressive systems tract of the Upper Miocene-Sarmatian Ser-3 eustatic cycle, at Sajóbábony, northern Hungary, was performed via petrographic, mineralogical and geochemical analyses. The purpose of the work was to analyze the degree of alteration of the volcanogenic sediments, as an indicator of the relative volcanic sedimentation rate. This may have an important role in indicating volcanic periods synchronous with sedimentation or reconstructing the volcanosedimentary paleoconditions. Sample pairs were collected from each bentonite and tuff layer, and, to facilitiate microstratigraphic relations, samples were collected every 10 cm within bentonite layers. Mineralogical analyses were performed by X-ray diffraction and geochemical analyses by inductively coupled plasma-mass spectroscopy.

The CaO/K2O and Eu/La ratios correlate with each other and with a montmorillonite/X-ray-amorphous phase ratio, reflecting Ca and Eu incorporation associated with devitrification and smectite formation. In accordance with the current literature, these mineralogical and geochemical proxies can be related primarily to the weathering processes. Considering vertical distributions in a sequence-stratigraphic context, the Ca content and Eu/La values show that local peaks and Eu anomalies characteristic of acid tuffs show minima at flooding surfaces (FS). Within a bentonite layer, representing a single transgressive period, the repeated events of dust-tuff accumulations have been determined by K2O/CaO and La/Eu peaks, confirmed also by the Eu anomalies in the rare earth element (REE) patterns, thus leading to the conclusion that the level of alteration is closely correlated with the elimination of terrigenous input and a minimum in volcanic sedimentation rate allowing more intensive alteration of the deposited volcanic material. In the case of fine tuff beds, Eu anomalies on REE patterns reflect limited alteration at the bottom and more intensive alteration in the upper parts of the beds, reflecting the effect of infiltration of sea water into the pores.

Clay-rich deposits of Upper Cretaceous levels in the Taveiro (Reveles and S. Pedro) and Aveiro (Bustos) regions of west-central Portugal are economically and environmentally important, but detailed chemical and mineralogical characterization is lacking. The purpose of this study was to partially fill that gap by correlating the trace-element geochemistry (particularly the rare earth elements, REE) with the mineralogy of both the whole rock and of the <2 μm fraction along selected stratigraphic levels of the formations. The results will help the ceramics industry in the region and will be important in paleoreconstruction environmental studies.

Mineralogical and chemical characterizations were carried out using X-ray diffraction (XRD), X-ray fluorescence (XRF), and instrumental neutron activation analysis (INAA). The following clay-mineral associations were identified: (1) at Reveles — smectite, illite, and kaolin minerals; (2) at S. Pedro — kaolin minerals and illite; and (3) at Bustos — illite, kaolin minerals, and mixed-layer illite-smectite. The distribution of trace elements in the <2 μm fraction depended on the clay mineralogy, suggesting that the trace elements were incorporated in, adsorbed to, or even replaced major elements in the clays, as follows: (1) first-row transition elements, particularly Zn and Ga, were enriched when smectite predominated; (2) As, Rb, and Cs were enriched in this fraction of the S. Pedro deposit, the only one with Fe (oxyhydr)oxides and a high proportion of illite; and (3) REE were more concentrated when kaolin minerals predominated. Eu was enriched in the <2 μm fraction, which was due to preferential incorporation in the Fe (oxyhydr)oxides and/or carbonates.

Hydrothermal alteration led to development of the Yarıkçı clay deposit within the Mesozoic chlorite-, muscovite-, chlorite-muscovite-schist, and garnet-graphite phyllite units along NW–SE- and N–S-trending faults in Mihalıççık in western central Anatolia. The geological, mineralogical, and geochemical characteristics and genesis of this economically important clay deposit have not been examined in detail previously. The present study has attempted to fill this gap. Green smectitic and cream kaolinitic claystones are abundant with smaller amounts of gray illite, dark brown Fe oxides, and silica phases occurring as stockwork/fracture infill and stain/coating. These units are covered by a dark, hard, sharp-edged, and thick silica cap. Metamorphic units exhibit cataclastic texture due to tectonic activities. Muscovite is mostly degraded to kaolinite, and feldspars show sericitization and argillization. Kaolinite typically has a platy form with irregular margins and locally sub-rounded, book-like texture suggesting hydrolysis during the hydrothermal injections. The association of Fe oxides, cristobalite/tridymite/quartz, gypsum/anhydrite, and jarosite are indicative of intense hydrothermal activities and development of kaolinite under acidic geochemical conditions. The local enrichment of SiO2, Fe2O3, S, Cu, and Au also supports this suggestion. The leaching of Sr, Rb, Ba, and Zr, and the slight increase in LREE/MREE+HREE ratios together with the negative Eu and Ce anomalies suggest the selective dissolution of muscovite, garnet, feldspar, and pyroxene by the hydrothermal fluids. Thus, abundant claystones of smectite and kaolinite were formed via the increase in Al+Fe+Mg/Si and Al±Fe/Si ratios in the alkaline and acidic environment, respectively, under the tectonic control of hydrothermal activity as seen in the alteration of chlorite, muscovite, and feldspar in metamorphic units.

Limonite is mainly derived from weathering of Fe sulfide, iron-bearing carbonate, or silicate minerals. The weathering of Fe sulfide or carbonate minerals to yield limonite from the Tongling mineralization cluster has been studied extensively. Knowledge of the mineralogical and geochemical characteristics of the limonite from weathering of Fe-bearing silicate minerals is still incomplete, however. To address this, black limonite containing ilvaite (a silicate mineral) found in Yeshan iron deposit, Tongling, China, was studied using mineralogical and chemical analysis. The mineralogical characteristics indicated that Mn goethite was present as nano-granular (<15 nm) or acicular (50–100 nm long, ~10 nm wide, i.e. high length/width ratio) crystals with low crystallinity. Groutite, ramsdellite, and pyrolusite were identified in the limonite as ~5 nm nanoparticles, and coated on the goethite surface. Amorphous Fe-Mn phases and silica were highly developed in the limonite studied. Ilvaite crystals showed idiomorphic granular morphology and were replaced by Fe-Mn oxides/hydroxides; pyrite was also present as inclusions within the ilvaite and the ilvaite structural formula calculated was Ca1.04(Fe1.57Mn0.31Mg0.04)(Fe1.09Al0.01)[Si1.95O]O(OH). According to the relatively high CuO and ZnO values and the low Al2O3 value in the black limonite, the negative correlations between (Fe2O3+MnO) and (CuO+ZnO+BaO), (Fe2O3+MnO) and Al2O3, high Mn and Si contents, and the characteristics of the textural relationships and compositions between the black limonite and ilvaite, a semi-enclosed environment with acidic to weakly alkaline conditions was deduced; ilvaite was found to be responsible for the formation and enrichment of limonite.

Caliche in various forms, namely powdery, nodule, tube, fracture-infill, laminar crust, hard laminated crust (hardpan), and pisolitic crust, is widespread in the Mersin area in southern Turkey. It generally occurs within and/or over the reddish-brown mudstone of the Kuzgun Formation (Tortonian, Miocene) and alluvial red soils of the Quaternary. The mineralogical distribution along representative caliche profiles was examined by X-ray diffraction, scanning electron microscopy, differential thermal analysis-thermal gravimetry, and chemical techniques. Calcite is the most abundant mineral associated with minor amounts of palygorskite in caliche samples, whereas smectite is prevalent mainly in the reddish-brown mudstone and alluvial red soils of the caliche parent materials and is associated with appreciable amounts of palygorskite. These minerals are also accompanied by trace amount of illite, quartz, feldspar, and a poorly crystalline phase. Palygorskite fibers and fiber bundles were developed authigenically on euhedral or subhedral calcite crystals of the caliche units and at the edges of smectite flakes in the caliche host-rocks or sediments. Intense, continuous evaporation of subsurface soil-water resulted in an increase in pH and the dissolution of detrital smectite within the red mudstones and alluvial red soils that enclose the isolated caliche forms, and caused an increase in the Al+Fe and Mg/Ca ratio, favoring the formation of palygorskite under alkaline conditions. The calcium required for caliche formation may have originated from eolian dust, detrital carbonate minerals, and/or other caliche materials, which are dissolved by carbonic acid.

The origins of dolocrete and associated palygorskite in the Çanakkale region of Turkey have been little studied, but are of fundamental importance for a more complete understanding of the mineralogy of this region. The present study was undertaken in order to narrow this gap. Siliciclastic red mudstones within alluvial-fan deposits of the Middle Miocene Sariyer Formation locally contain dolocretes in various forms (powdery, nodular, and fracture-filling) and scarce matte-brown, authigenic clay lenses. The mineralogical characteristics of dolocrete and authigenic clay lenses were examined using polarized-light microscopy, X-ray diffraction, differential thermal analysis and thermal gravimetry, scanning-electron microscopy, and infrared spectroscopy, as well as by chemical and isotopic methods. These analyses indicate that the dolocretes are indeed predominantly dolomite, coexisting with variable amounts of palygorskite. The authigenic clay lenses are composed mainly of palygorskite. Dolomite appears as euhedral crystals, whereas palygorskite developed authigenically as interwoven fibers on and between resorbed dolomite crystals, rimming euhedral crystals, and as fiber bundles (where dolomite ± magnesite is absent). The stable-isotope values and some petrographic features, such as alveolar texture and dolomite needles, support a pedogenic origin for the dolocretes. In the initial stage, dolomite formed by replacement of siliciclastic red mudstones and/or by precipitation from percolating soil-derived water in a near-surface setting. Subsequently, palygorskite either precipitated on the dolomite crystals from relatively more evaporative water, replaced the host-rock mudstone in the presence of Al + Fe, or formed directly from solution where the Ca/Mg ratio decreased and the Al + Fe increased. In view of the large Cr and Ni contents of the bulk-rock samples, the elements required for the crystallization of dolomite and palygorskite (namely Mg, Ca, Si, Al, and Fe) may have been supplied by weathering of ophiolitic rocks that crop out in the area.

Widespread alteration in the Miocene lacustrine volcanic/sedimentary rocks of the Ankara-Çankiri basin of central Anatolia has resulted in the formation of sizeable (economic) quantities of bentonite deposits. No detailed characterization of the geological, mineralogical, and geochemical properties or the depositional environments of these primary and secondary bentonite deposits has been carried out to date. The present study was undertaken to close this knowledge gap. Two possible hypothetical processes were examined to explain the genesis of the bentonites: 1) The bentonites were formed by the devitrification of volcanic glass in a lacustrine setting; and 2) The bentonites were formed by the chemical weathering of previously deposited volcaniclastic sediments and ophiolitic materials. The characteristics of the bentonites were examined using X-ray diffractometry, scanning and transmission electron microscopy, energy dispersive spectroscopy, and chemical analyses of major and trace elements. The Ankara-Çankırı bentonites are found gradationally interbedded with parent Miocene volcanic and volcaniclastic rocks. These bentonites were deposited in a shallow lacustrine setting based on observed desiccation cracks, locally enclosed coal seams, plant rootlets, gypsum lenses, yellow sulfate-like fracture infillings, and ferric iron oxide stains. Smectite resulted from the chemical weathering of feldspar and possibly also the weathering of biotite and hornblende. This smectite was precipitated in situ on partially dissolved glass and feldspar. The average major-element composition of the smectite-rich clay fractions yielded the following montmorillonitic smectite structural formula: (Na0.33Ca0.31K0.18) (Al2.35Fe0.80Mg0.78)(Si7.79Al0.21)O20(OH)4.

The interlayer cation occupancy in the smectite-rich clay fractions was based on the use of Na+/(Na++Ca2+) ratios and showed a composition between a Ca-smectite and a Na-smectite. The relative increases in several groups of elements according to the LREE/(MREE+HREE) ratio, Al2O3, the sum of Ni+Co+Cr, the sum of Fe2O3+MgO+TiO2, the positive correlation between Rb+Ba and Na2O+K2O, Sr and Rb, Rb/Sr and Zr, Zr/Sm and SiO2, the negative Eu anomaly, and the field and petrographic observations further showed that the Si, Al, Fe, and Mg required to form smectite were mainly supplied from the decomposition of feldspars, amphiboles, and volcanic glass from volcanic materials and were partially supplied from the chemical weathering of ophiolitic basement units. The bentonite deposits examined in this study are mainly primary bentonites derived from volcanics and local secondary bentonites from previously deposited volcaniclastic sediments and ophiolitic materials.

Kaolin samples from the Jari deposit (Amazon region) were studied using various techniques to characterize its structural and crystallochemical aspects, and to establish its origin and evolution. A profile 60 m thick was selected in a kaolin mine (Morro do Felipe) located at the banks of the Jari river. Despite the great thickness of the deposit and the variety of kaolin types, the mineralogical composition is rather homogeneous and is mainly kaolinite associated with gibbsite and small amounts of quartz, anatase, goethite and hematite. The field observations and the morphological analysis indicate the existence of sedimentary features throughout the whole profile except for the upper aluminous clayey layer (Belterra Clay). This is evidence that the Rio Jari kaolin deposit originated from sedimentary material, the Alter do Chão Formation. The presence of alternating clay and sandy layers is explained by sedimentation processes with great depositional energy variation. Thus, the accumulation of thick clay layers was related to a low-energy phase, and during the high-energy phases, the deposition process led to the accumulation of sandy materials, constituted essentially of quartz and showing strong textural and structural variation. Later on, periods of hydromorphy were responsible for iron removal and consequently for the bleaching of the sedimentary formation. The crystallinity data show an increase of the structural disorder toward the surface associated with an increase in the amount of structural Fe in the kaolinite. The Rio Jari kaolin deposits should be considered as having originated from kaolinitic clay sediments of the Alter do Chão formation (protore) that was submitted to intensive lateritic weathering processes.