Tuffs of the Tertiary Colbún Formation near Quinamávidain central southern Chile have been mapped and their mineralogy analyzed. The pyroclastic rocks present a maximum outcropping thickness of 120 m and are dominated by vitreous lapilli and minor lithic tuffs, the products of active volcanism nearby. About 10% of the tuffs consist of lenses of fine banded tuffs with a high leaf content that were deposited in shallow lakes during quiescent periods between periods of volcanic activity. This tuff sequence is pervasively transformed to clinoptilolite/heulandite and mordenite with variable amounts of plagioclase, minor quartz and smectite. Factors thought to have influenced this conversion to zeolites are a humid climate following deposition combined with a slightly elevated heat flow. Local hydrogeological conditions have modified the cation-hydrogen ion ratios across the study area favoring the formation of clinoptilolite/heulandite and mordenite with medium-minor smectite in the center and south, and a more abundant presence of smectite in the north of the study area.

The composition of altered volcanic ash of the Late Ordovician Kinnekulle bed was studied in geological sections of the Baltic Paleobasin. The composition of altered ash varies with paleosea depth from northern Estonia to Lithuania. The ash bed in shallow shelf limestones contains an association of illite-smectite (I-S) and K-feldspar, with the K2O content ranging from 7.5 to 15.3%. The limestone in the transition zone between shallow- and deep-shelf environments contains I-S-dominated ash with K2O content from 6.0 to 7.5%. In the deep-shelf marlstone and shale, the volcanic ash bed consists of I-S and kaolinite with a K2O content ranging from 4.1 to 6.0%. This shows that authigenic silicates from volcanic ash were formed during the early sedimentary-diagenetic processes. The composition of the altered volcanic ash can be used as a paleoenvironmental indicator showing the pH of the seawater or porewater in sediments as well as the sedimentation rate.

Pliocene volcaniclastic lacustrine rocks of the Doğanbey formation in the Beyşehir region (central Anatolia) are composed of organic-matter-bearing claystone, clastic units and dolomite interbeds, suggesting an anaerobic, shallow swampy, lacustrine depositional environment. The depositional environment was subjected to periodic climatic change during which diagenesis occurred, and smectite, and locally palygorskite, were precipitated. Smectite flakes formed authigenically on feldspar and palygorskite fibers between dolomite rhombs and at the edges of smectite flakes. Increases in leaching of Na, K, Sr, Ba and Rb, increasing Al/Si ratios, and Fe with increasing degree of alteration reveal that hydration of volcaniclastic grains (feldspar, glass) by meteoric water — determined from O and H isotopic values — was the main cause of precipitation of beidellite and montmorillonite based on the tetrahedral charge/octahedral charge ratio, with average structural formulae of (Si7.72Al0.28)(Al3.20Fe0.53Mg0.25 Mn0.02Ti0.04) (Ca0.11Na0.09K0.11), and (Si7.88Al0.13)(Al3.18Fe0.53Mg0.18Mn0.02Ti0.05)(Ca0.11Na0.11K0.09), respectively. Therefore, the Doğanbey-area smectite is presumed to have formed by chemical weathering and dissolution-precipitation from feldspar and glass during diagenesis; palygorskite formed by direct precipitation from Mg-rich solutions during dolomitization, and by transformation from smectite in an alkaline lacustrine environment.

A siliceous sinter collected from Octopus Spring in Yellowstone National Park, USA contains an occluded volcanic rock fragment that has undergone alteration. The sinter piece beyond the fragment is mostly dominated by opal-A with trace amounts of bacterial cells, calcite and detrital quartz. Within the altered rock region, the mineral assemblage is dominated by dioctahedral smectite and quartz with trace amounts of pseudobrookite, ilmenite, rutile and hematite. Onset of opal-CT formation was only found in the outer spicular region of the sinter, which is unexpected given that this outer part represents newest growth. A reaction mechanism is proposed whereby the alteration of feldspar to smectitic clay locally produces excess silica, and alkali metal, and raises pH. As the clay mineral forms, it sequesters ions from pore fluids thereby inhibiting the opal-A phase change to more ordered opal-CT. Ions such as Mg are known to promote the opal-A to opal-CT reaction. Smectite formation therefore may assist microbial-texture preservation processes as excess silica produced increases the rate at which primary opal-A is formed. The altered zone also retains the greatest amount of fixed C and fixed N (operationally defined as C and N retained upon combustion at 450°C). The fixed N probably represents ammonium trapped in the exchangeable interlayer site of the smectite. This fixed N may serve as a potential biological signature of microbial activity in ancient rocks formed in similar environments.

The Clay Minerals Society published a complete characterization scheme for its ‘Source Clays’ but not for its ‘Special Clays’. To address this issue, the specific surface areas (SSAs) of the 16 special clays from The Clay Minerals Society were determined using the Brunauer, Emmett and Teller (BET) method of adsorption of an inert gas. Two BET measurements were performed for each of the 16 special clays, and the average BET SSA of each of the special clays was determined. The BET SSA of cookeite is reported for the first time. In the present study, special clays from The Clay Minerals Society are classified under three groups based on their BET special surface area values as Group-I special clays, with BET values of 0.1–10 m2/g, Group-II special clays, with BET values of 10–100 m2/g, and Group-III special clays, with BET values >100 m2/g. Comparisons which proved interesting were the those involving the mixed-layer clays and the synthetic clays. The systematic approach employed in this paper will allow for better comparisons to be made between different clays and will provide a comprehensive database for future applications of such material (e.g. as catalyst carriers, as adsorbents in waste treatments, etc.).

The Allou Kagne (Senegal) deposit consists of different proportions of palygorskite and sepiolite, and these are associated with small quantities of quartz and X-ray amorphous silica as impurities. No pure palygorskite or sepiolite has been recognized by X-ray diffraction. Textural and microtextural features indicate that fibrous clay minerals of the Allou Kagne deposit were formed by direct precipitation from solution. Crystal-chemistry data obtained by analytical/transmission electron microscopy (AEM/TEM) analyses of isolated fibers show that the chemical composition of the particles varies over a wide range, from a composition corresponding to palygorskite to a composition intermediate between that of sepiolite and palygorskite, but particles with a composition corresponding to sepiolite have not been found. Taking into account the results from selected area electron diffraction and AEM-TEM, fibers of pure palygorskite and sepiolite have been found but it cannot be confirmed that all of the particles analyzed correspond to pure palygorskite or pure sepiolite because both minerals can occur together at the crystallite scale. In addition, the presence of Mg-rich palygorskite and very Al-rich sepiolite can be deduced.

It is infrequent in nature that palygorskite and sepiolite appear together because the conditions for simultaneous formation of the two minerals are very restricted. The chemical composition of the solution controls the formation of the Allou Kagne sepiolite and palygorskite. The wide compositional variation appears as a consequence of temporary variations of the chemical composition of the solution.

Clay particle aggregation affects a number of environmental processes, such as contaminant sorption/desorption, particle movement/deposition, and sediment structure and stability, yet factors that control clay aggregation are not well understood. This study was designed to investigate how microbial reduction of Fe(III) in clay structure, a common process in soils and sediments, affects clay-particle aggregation. Microbial Fe(III) reduction experiments were conducted with Shewanella putrefaciens CN32 in bicarbonate buffer with structural Fe (III) in nontronite as the sole electron acceptor, lactate as the sole electron donor, and AQDS as an electron shuttle. Four size fractions of nontronite (D5–D95 of 0.12–0.22 µm, 0.41–0.69 µm, 0.73–0.96 µm and 1.42–1.78 µm) were used to evaluate size-dependent aggregation kinetics. The extent of Fe(III) bioreduction and the amount of exopolysaccharide (EPS), a major biopolymer secreted by CN32 cells during Fe(III) bioreduction, were measured with chemical methods. Nontronite particle aggregation was determined by photon correlation spectroscopy and scanning electron microscopy. The maximum extent of Fe(III) bioreduction reached 36% and 24% for the smallest and the largest size fractions, respectively. Within the same time duration, the effective diameter, measured at 95% percentile (D95), increased by a factor of 43.7 and 7.7 for these two fractions, respectively. Because there was production of EPS by CN32 cells during Fe(III) reduction, it was difficult to assess the relative role of Fe(III) bioreduction and EPS bridging in particle aggregation. Thus, additional experiments were performed. Reduction of Fe(III) by dithionite was designed to examine the effect of Fe(III) reduction, and pure EPS isolated from CN32 cells was used to examine the effect of EPS. The data showed that both Fe(III) reduction and EPS were important in promoting clay mineral aggregation. In natural environments, the relative importance of these two factors may be dependent on local conditions. These results have important implications for understanding factors in controlling clay particle aggregation in natural environments.

Fougerite (IMA 2003-057) is a mixed M(II)-M(III) hydroxysalt of the green rust group, where M(II) can be Fe or Mg, and M(III) is Fe. The general structural formula is: ${[{\text{Fe}}_{1-}^{2+}x{\text{Fe}}_x^{3+}{\text{Mg}}_y{(\text{OH})}_{2+2y}]}^{+x}{[x\text{/}n{A}^{-n}.m{\text{H}}_2\text{O}]}^{-x}$ where A is the interlayer anion and n its valency, with 1/4 ≼ x/(1+y) ≼ 1/3 and m ≼ (1−x+y). The structure of green rusts and parent minerals can accommodate a variety of anions, such as OH−, Cl−, ${\text{CO}}_3^{2-},{\text{SO}}_4^{2-}$${\rm{CO}}_3^{2 - },\;{\rm{SO}}_4^{2 - }$. The structure of the mineral was studied by Mössbauer, Raman and X-ray absorption spectroscopies (XAS) at the FeK edge. Mössbauer spectra of the mineral obtained at 78 K are best fitted with four doublets: D1 and D2 due to Fe2+ (isomer shift δ ≈ 1.27 and 1.25 mm s−1, quadrupole splitting ΔEQ ≈ 2.86 and 2.48 mm s−1, respectively) and D3 and D4 due to Fe3+ (δ ≈ 0.46 mm s−1, ΔEQ ≈ 0.48 and 0.97 mm s−1, respectively). Microprobe Raman spectra obtained with a laser at 514.53 nm show the characteristic bands of synthetic green rusts at 427 and 518 cm−1. X-ray absorption spectroscopy shows that Mg is present in the mineral in addition to Fe, that the space group is and the lattice parameter a ≈ 0.30–0.32 nm. The mineral forms by partial oxidation and hydrolysis of aqueous Fe2+, to give small crystals (400–500 nm) in the form of hexagonal plates. The mineral is unstable in air and transforms to lepidocrocite or goethite. The name is for the locality of the occurrence, a forested Gleysol near Fougères, Brittany, France. Its characteristic blue-green color (5BG6/1 in the Munsell system) has long been used as a universal criterion in soil classification to identify Gleysols. From a thermodynamic model of soil-solution equilibria, it was proposed that for the eponymous mineral, Fougères-fougerite, OH− may be the interlayer anion. In other environments, the interlayer anion may be different, and other varieties of fougerite may exist. Fougerite plays a key role in the pathways of formation of Fe oxides.

Investigation of material from three core sections of the RWTH-1 drill-hole in the Wurm syncline of Aachen, Germany, shows mineralogical and structural evidence of intensive hydrothermal activity in the footwall of the Aachen thrust. Mineral and microstructural data indicate minimum temperatures of 200–250°C. CISillite 001 values of 0.45–0.61 (Δ°2θ) and insignificant amounts of smectite indicate a late diagenetic grade for illite pointing to temperatures <200°C. Chlorite, mainly formed in veins and cleavage planes, has CISchlorite 002 values between 0.35 and 0.26 (Δ°2θ) which only in part point to anchizonal grade. In contrast to these illite and chlorite data, maximum temperatures up to 370°C can be expected based on comparison with recently published fluid inclusion and mineral thermometric data. Illite is neither significantly affected by the hydrothermal event nor by deformation, and mirrors the burial history of the Wurm syncline.

Chlorite grew syntectonically as is shown by bent and predominantly stretched sheets which do not, however, have deformed structures. Syntectonic hydrothermal growth by incipient nucleation along crystal edges limited domainsize and thus also the CISchlorite 002 values. The hydrothermal event did not last long enough to allow further crystal growth. The retarded CISillite and CISchlorite grades can be best explained by limited duration(probably <5000 y) of the hydrothermal event which for a short time reached epithermal temperatures. The hydrothermal fluid flow was caused by dewatering of sedimentary rocks during thrusting and tectonic thickening within the Variscan orogen and it was focused along the Aachen thrust which represents the frontal Variscan thrust.

Adsorption by synthetic 2-line ferrihydrite and hematite of glyphosate and phosphate, separately and together, was compared with adsorption results for goethite, gibbsite and two kaolinites in order to determine adsorption differences and similarities, in particular competition and phosphate preference, of these variable-charge minerals. Hematite rapidly adsorbed both compounds, while adsorption by ferrihydrite was slow, in particular of glyphosate, probably because of very slow diffusion of the bulky glyphosate molecules into interior sites in ferrihydrite particles. Accordingly, the Langmuir adsorption capacity of glyphosate (GAC) was considerably smaller (1.85 µmol m−2)than GAC for hematite (2.61 µmol m−2). The phosphate adsorption capacities (PAC) for ferrihydrite and hematite were more alike, 2.91 µmol m−2 and 2.85 µmol m−2, respectively. Differences between surface coordination (mono- or bidentate) may also contribute to the observed differences but conflicting information about the nature of the surface complexes makes this a difficult contributary factor to assess. The minerals were found to exhibit great variation in extent of competition and phosphate preference. Little competition and phosphate preference characterized hematite adsorption, while phosphate almost completely outcompeted glyphosate on goethite; ferrihydrite adsorption fell between these extremes. These differences may be attributed to different numbers of common (competitive) and specific (selective) adsorption sites on the three Fe oxides with a decreasing number of common sites in the order: goethite>>ferrihydrite>hematite, i.e. almost all goethite sites are common but with strong phosphate preference, while most hematite sites are specific for either glyphosate or phosphate. Alternatively, the result may be explained by adsorption in more planes, e.g. glyphosate adsorption onto the inner-Helmholtz-plane-adsorbed phosphate. For all six minerals compared, desorption of glyphosate following phosphate addition was found to be significantly correlated with the difference between the amounts of phosphate and glyphosate adsorbed indicating that this difference may be used as a competition index for predicting the influence of phosphate on glyphosate adsorption.

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.

The processes of clay mineral formation were studied in seven podzol profiles developed on granitic regoliths in the Polish part of the Tatra Mountains. The selected profiles have similar parent material and macroscopically represent different stages of soil development (from initial to advanced). Bulk soil material (<2 mm fraction) and separated clay fractions (<2 µm) were studied using a petrographic microscope, X-ray diffraction, Fourier transform infrared spectroscopy, and scanning electron microscopy-energy-dispersive spectrometry methods. The mineral compositions of the bulk soil samples are more or less the same (quartz, feldspars, mica and minor amounts of other phyllosilicates). The clay fractions are composed of mica and mixed-layer minerals which contain hydrated interlayers of vermiculitic and/or smectitic type, and kaolinite. Smaller amounts of chlorite, feldspars and quartz were also identified. Chlorite is present almost exclusively (except for one profile) in lower soil horizons (C, B/C, B). The amount of minerals with hydrated interlayers increases up the profiles. Kaolinite is present in all the samples except for the lowermost soil horizons (C) of two of the profiles. In some of the B horizons, the formation of hydroxy interlayers within hydrated interlayers is observed. The main processes of clay mineral formation recognized in the soils studied are: inheritance from the parent rocks; crystallization of kaolinite from soil solutions; the formation of dioctahedral vermiculite at the expense of inherited dioctahedral mica, and the formation of dioctahedral smectite at the expense of vermiculite. The recognized sequence of transformation is as follows: M → R0 M-V (12 Å or 14 Å) → R0 M-12 Å V → R1 M-12 Å V → 12 Å V → V-S → S. Observed formation of hydroxy interlayers seems to be pH dependent, starting when the pH ⩾ 4.4. The process of dissolution of primary silicates occurring simultaneously with the transformation is also documented.

Nano-ball allophane is a hydrous Al silicate with a hollow-sphere morphology that contains some defects or pores along the spherule walls. Enlargement of the pore openings by dilute alkali treatment was confirmed by cation exchange capacity determinations using various alkylammonium cations as replacement cations. An allophane sample with a low Si/Al ratio (0.67) was equilibrated with 10 mM CaCl2 (pH = 6.0) and the Ca2+ retained was extracted using aqueous 1 M NH4C1 or alkylammonium chloride salts. The Ca2+ extracted by ${\text{NH}}_4^{+}$ was 15.1 cmolc kg−1, but ${\text{CH}}_3{\text{NH}}_3^{+}$${\rm{C}}{{\rm{H}}_3}{\rm{NH}}_3^ + $ (mean diameter = 0.38 nm) only extracted 7.9 cmolc kg−1 of Ca2+. After 10 mM NaOH treatment (0.25 g:100 mL) of the allophane, the Ca2+ extracted by ${\text{NH}}_4^{+}$${\rm{NH}}_4^ + $ was 29.7 cmolc kg−1, 29.6 cmolc kg−1 by ${\text{CH}}_3{\text{NH}}_3^{+}$${\rm{C}}{{\rm{H}}_3}{\rm{NH}}_3^ + $, and 29.4 cmolc kg−1 by ${{\text{(CH}}_3\text{)}}_2{\text{NH}}_2^{+}$${{\rm{(C}}{{\rm{H}}_3}{\rm{)}}_2}{\rm{NH}}_2^ + $. The extraction of Ca2+ by the large ${\text{C}}_2{\text{H}}_5{\text{NH}}_3^{+}$${{\rm{C}}_2}{{\rm{H}}_5}{\rm{NH}}_3^ + $ cation (mean diameter = 0.46 nm) only decreased to 26.1 cmolc kg−1, indicating that pore diameters were enlarged from ∼0.35 to 0.45 nm. The significant increase in Ca2+ retention after NaOH treatment was attributed to the dissociation of increased numbers of newly exposed silanol groups in the enlarged pores. The low Si/Al ratio of the NaOH-dissolved material (0.35) and the decreased intensity of the 348 cm−1 IR band also suggested selective dissolution of the pore region. For allophane with a high Si/Al ratio (0.99) and much accessory polymeric Si, dissolution of polymeric Si and of the pore region occurred simultaneously. Alkali treatment produced a smaller increase in pore size and Ca2+ retention for allophanes with large Si/Al ratios than for allophanes with small Si/Al ratios. It was concluded that by altering the dilute alkali treatment conditions and varying the Si/Al ratio of allophane, the extent of structural modification or pore enlargement of the hollow spheres might be controlled.

A novel method for the analysis of clay minerals using Fourier transform infrared spectroscopy is presented. Clay mineral suspensions are dried on a Si wafer substrate for transmission infrared (IR) analysis. Four natural Source Clays from the Source Clays Repository of The Clay Minerals Society, SWy-2, SAz-1, SHCa-1 and KGa-1b, as well as the synthetic hectorite, Laponite RD, were analyzed using the described method with signal to noise (s/n) ratios in excess of 100,000 for the strongly absorbing Si-O stretching frequency. Scanning electron microscopy (SEM) images show that the mineral films possess suitable uniformity and low surface roughness for transmission IR measurements that is confirmed by minimal deviations in the baseline of collected IR spectra. The IR spectra are generated and peak locations are compared to previously reported values, generated from KBr pellet and attenuated total reflectance methods.

Floating, mixed-valent Fe films have been observed worldwide in wetlands, ferrous iron-rich seeps, and in seasonally reduced soils, but are usually misidentified as oil or biofilms. There has been little characterization or explanation of their formation. Along the Oregon coast such films were found on ephemeral pools where Fe(II)-rich groundwater (∼100 µM Fe) has been discharged at the base of Pleistocene sand dunes. Fe(II) oxidized to Fe(III) at the air-water interface to form ∼100–300 nm thick films. Analyses indicated that the films contained both Fe(III) and Fe(II) in a ratio of 3:1; Si was the other main cation; OH was the main anion and some C was also identified. The film morphology was flat under optical and electron microscopy with some attached floccules having a string-like morphology. Energy-filtered electron diffraction patterns showed three diffraction rings at 4.5, 2.6 and 1.4 Å in some places and two rings (2.6 and 1.4 Å) in others. Upon further oxidation the films became 2-line ferrihydrite. We are proposing the name ‘schwimmeisen’ for the floating, mixed-valent Fe film.

An ab initio theoretical approach has been used to calculate optimized geometries and the relative energies of various compositional arrangements in structures of dioctahedral smectites based on models consisting of two unit-cells. These calculations indicate that the energy differences between structures having vacancies in sites with cis- or trans-OH coordination are small and that their relative energies vary with the chemical nature of the substitutions. For example, a cis-OH coordination for the vacancy was the most stable when the interlayer charge originated from substitution of Al for Si in the tetrahedral sheet, whereas the trans-coordination was the more stable for most cases of substitution in the octahedral sheet, an exception being Fe(II) for Al where the cis-OH coordination was favored. It seems likely, therefore, that long-range structural disorder will be a common phenomenon in natural phyllosilicate specimens.