The exact nature of self-consciousness is a problem that has occupied a central position in contemporary philosophical thought. Despite a wide variety of approaches, however, a common assumption in almost all theories is that adult consciousness functions as the norm and appropriate starting point for an investigation in this area. Indeed, in general, philosophers have made the presupposition that they can deal with issues in their field - whether, for example, this involves emotions, knowledge, or perception - purely as these are manifest in an adult form.

X-ray diffraction (XRD) characterization of natural and intercalated smectites is usually limited to the apparent d-value estimated from the peak maxima in the raw data. This can lead to the misinterpretation of the measured data. In the case of XRD, the interference function is modulated by instrumental factors (Lorentz-polarization factor, diffraction geometry) and physical factors (structure factor, surface roughness effect). These effects lead to diffraction profile distortions, depending on the diffraction angle and peak full width at half maximum (FWHM). As a result, the diffraction profiles for structures with large line broadening (FWHM > 1°) exhibit a significant peak shift (Δd ∼ 1.5 Å), especially at low angles (2θ ≤ 10°). The present work deals with the detailed analysis of all these effects, their corrections and their consequences for the interpretation of diffraction patterns (including possible errors in determining lattice parameters or the structure model). The investigated materials were montmorillonites (MMT) intercalated with hydroxy-Al polymers. Diffraction profile analysis revealed the corrected d-values and showed that the intercalated sample is not a mixed-layered structure. As a result a structural model of the interlayer is presented.

Results are presented of a diagenetic study from the 1300 m thick Oligocene Molasse deposits penetrated by the Thônex geothermal exploration well (Geneva, Switzerland). The x-ray diffraction (XRD) studies of fine-grained rocks indicate the following diagenetic changes: a decrease of illite/smectite (US) expandability from approximately 90% to 30% with depth, a decrease of the amount of US in the clay mineral fraction, and the appearance of corrensite at depths >750 m. The transition from random US to ordered I/S occurs at the base of the Thônex well (1200 to 1300 m) and is associated with a coal rank of about 0.7% Rr (mean random vitrinite reflectance) corresponding to paleotemperatures of 110 to 115 °C Corrensite appears at a vitrinite reflectance value of 0.6% Rr and a corresponding paleotemperature of 100 °C. The amount of post-Molasse erosion is estimated to be approximately 2 km. Thermal history modeling of the Thônex well suggests maximum paleotemperatures of 80 to 115°C and an average paleogeothermal gradient of 27 °C/km during Late Miocene maximum burial conditions.

Unesco's first Philosophical Encounters were held last year at Paris on the theme of “What Do We Not Know?” and they were a great success. Diogenes published some of the papers by participants in its No. 169. A second meeting was held from March 27-30, 1996, devoted to a question as simple and difficult as that of the first: “Who Are We?” Once again this journal will not be able to publish all contributions, but is fortunate enough to present at least some of them to its readers.

Samples containing spherical kaolinite, synthesized under hydrothermal conditions (T = 200 °C; t = 24 h, 192 h, 720 h) from gel with Si/Al = 0.84, were studied by differential thermal analysis/thermogravimetry (DTA/TG) to provide a contribution to the mineralogical characterization of this unusual morphology. The data clearly show that dehydroxylation temperature of spherical kaolinite is lower than that of platy/lath kaolinite. It can also be used to detect the presence of spheres in the presence of the other morphologies. A rough estimation of its quantity can be obtained by TG data if spheres are present in appreciable concentrations. The results also confirm microscopic observations previously reported in the literature: spherical morphology is a discrete and metastable phase, and it is gradually dissolved along hydrothermal treatments of gels.

Batch sorption experiments at fixed initial Np(V) concentration (∼1 × 10−6 M 237Np), M/V ratio (4 g L−1), and ionic strength (0.1 molal NaNO3) were conducted to determine the effects of varying pH and $P_{C{O}_2}$ on Np(V) sorption on SAz-1 montmorillonite. The results show that Np(V) sorption on montmorillonite is strongly influenced by pH and $P_{C{O}_2}$. In the absence of CO2, Np(V) sorption increases over the entire pH range examined (∼3 to ∼10), with measured sorption coefficients (KD) of about 10 mL g−1 at pH < 6 to KD ∼ 1000 mL g−1 at a pH of 10.5. However, for experiments open to atmospheric CO2 ($P_{C{O}_2}={10}^{-3.5}atm$), Np(V) sorption peaks at KD ∼ 100 mL g−1 at pH of 8 to 8.5 and decreases at higher or lower pH. A comparison of the pH-dependence of Np(V) sorption with that of Np(V) aqueous speciation indicates a close correlation between Np(V) sorption and the stability field of the Np(V)-hydroxy complex NpO2OH0 (aq). In the presence of CO2 and aqueous carbonate, sorption is inhibited at pH > 8 due to formation of aqueous Np(V)-carbonate complexes. A relatively simple 2-site Diffuse-Layer Model (DLM) with a single Np(V) surface complexation reaction per site effectively simulates the complex sorption behavior observed in the Np(V)-H2O-CO2-montmorillonite system. The good agreement between measured and DLM-predicted sorption values suggests that surface complexation models based on parameters derived from a limited set of data could be useful in extrapolating radionuclide sorption over a range of geochemical conditions. Such an approach could be used to support transport modeling and could provide a better alternative to the current use of constant KD values in performance assessment transport calculations.

This paper is interested first of all in the gender polarities (male-female), as well as the doctrinal ones (heresy-orthodoxy), present in Sicut aquila, that is, the last eight chapters of Suso's Life. However, the theme of heresy had already been touched on in a text from his youth, in particular with regard to Suso's encounter with a ‘nameless wild thing’, whose sex is somewhat uncertain. Various earlier legends evoking similar ‘androgynous encounters’ help us to see that in the Middle Ages the theme of the androgyne also had something to do with the philosopher's stone of the alchemists. In Suso's writing this stone is embodied by Christ, whose iconography contains androgynous characteristics. But the gender polarity of Sicut aquila is expressed above all through a romantic metaphysical flight written in the form of a lovers’ dialogue between Suso - sometimes called Frater Amandus - and his beloved spiritual daughter.

The K-Ar systematics of illite/smectite (I/S) mixed layers in deeply buried shales from the Gulf Coast, the North Sea and the Mahakam Delta basins have been compared to provide additional perspectives on the diagenetic evolution of these minerals. Comparison of the results suggests that illitization proceeds similarly in the 3 basins, at least for the increase in the illite-layer and K contents, despite differences in the provenance of the detrital components, the ages of deposition, the depths of burial and the tectonic history of the basins. Analysis of the trends with depth in the illite-layer and K contents of I/S-enriched size fractions of shales in the North Sea and the Mahakam Delta basins shows that these trends represent segments of the more complete trends from I/S minerals of the Gulf Coast area.

The trends with depth in the radiogenic 40Ar contents and in the K-Ar ages of the I/S-rich fractions in the North Sea and Mahakam Delta basins suggest that, relative to the reference trends of the Gulf Coast area, the K-Ar system of the clay material is more dependent on the behavior of the radiogenic 40Ar than on the occurrence or non-occurrence of detrital grains in the size fractions. Recasting of the available data suggests that retention of radiogenic 40Ar by the illite-type minerals occurs in the intense illitization zone and release occurs in the deeper part of the basins. We therefore speculate that the illitization process of the I/S mixed layers of progressively buried shale-type sediments could be controlled by a transformation process integrating dissolution of detrital components in poral rock environments relatively impermeable to radiogenic 40Ar. These excesses, which might be partly or completely erased in deeper parts of the sedimentary basins, question the application of the K-Ar dating method on clay minerals extracted from shales.

The chemical composition of mixed-layer serpentine/chlorite (Sp/Ch) in Tuscaloosa Formation sandstone was analyzed by energy dispersive X-ray spectroscopy (EDX) in the scanning electron miscroscope (SEM) and by X-ray diffraction (XRD). EDX results indicate little depth-controlled variation in composition, whereas XRD results suggest distinct decreases in octahedral Fe and tetrahedral Al. XRD-determined compositions appear to be erroneous and actually reflect progressive changes in Sp/Ch unit-cell dimensions caused by polytype transformations of Ibb layers to Iaa layers in a mixed-layer Ibb/Iaa polytype. The relative lack of variation in Sp/Ch composition, especially when compared to other studies of chlorite minerals over similar temperature ranges, is attributed to a reaction mechanism whereby mineralogic transformations (serpentine layers to chlorite layers and Ibb layers to Iaa layers) occur on a layer-by-layer basis within coherent crystallites, rather than by dissolution-precipitation crystal growth.

The lack of titanium in chlorite minerals is attributed to high levels of octahedral Al3+ that prohibit inclusion of the highly charged Ti4+ in the octahedral sheet. Anatase (TiO2) in the Tuscaloosa Formation apparently formed when Ti was liberated during crystallization of Sp/Ch following the breakdown of a Ti-bearing precursor (detrital ultramafic clasts and/or odinite). Odinite, an Fe-rich 7-Å phyllosilicate that forms in some shallow marine sands, apparently existed as a short-lived, poorly crystallized intermediary between dissolution of the ultramafic clasts and formation of Sp/Ch.

The constitutions of the decolonized new nations were marked by the process of the devolution of power. This process had an impact on the agenda setting and arena setting embedded in these constitutions. ‘Agenda’ refers to the conduct of political affairs and ‘arena’ to the delimitation of the powers of Parliament, the design of constituencies, etc. As a special feature, federalism was introduced by several constitutions. It emerged as a device for the gradual devolution of power. In some instances it proved to be a permanent asset (India), in others it was contested (Nigeria) or rejected (Rhodesia). None of the new constitutions contained adequate provisions for the civilian control of the armed forces. The armed forces were simply taken for granted and their potential political role disregarded. But in many new nations political power was soon usurped by the armed forces and constitutional government was suspended.

An Fe-berthierine occurs in a buried laterite from the Late Cretaceous (Cenomanian) in southwestern Minnesota. It formed beneath a lignitic horizon in which reducing solutions percolated through a laterite comprising gibbsite, kaolinite and goethite. Morphologic differences suggest 2 separate conditions of Fe-berthierine formation. Early forms of Fe-berthierine include radial bladed or radial blocky crystallites coating pisoids, along with alteration of kaolinite at crystal boundaries. These morphologies formed in the vadose zone. Later forms precipitated under subaqueous conditions as macroscopic, pore-filling cement. The large size of the later-formed Fe-berthierines enabled microprobe characterization. This 1st reported occurrence of Mg-free berthierine has a structural formula close to an idealized Fe-berthierine: Fe2Al2SiO5(OH)4. Apart from their chemistry, the unique feature of the Minnesota Fe-berthierines is their formation in an exclusive nonmarine depositional environment. They formed in situ as part of a lateritic weathering profile developed on a broad, low relief peneplain. Physical evidence of formation under nonmarine conditions includes the presence of 1) scattered lignitic fragments; 2) concretions forming casts and molds of woody material; and 3) a nonmarine fossil (Unio sp. undet). Chemical evidence includes siderites collected from the berthierine-bearing horizon having stable isotope values indicating freshwater formation.

Vermicular glaucony grains observed by transmission electron microscopy (TEM) show three irregularly alternating zones. Zone A has a high degree of linear orientation, no void space, and relatively defect-free lattice-fringe images. Zone B has an amalgamated bundle texture with a sub-parallel, linear orientation of bundles to each other and to zone A. Zone B has little or no void space, and lattice images appear to be a combination of those typical of zone C with minor amounts of modified zone A forms. Zone C has a randomly oriented, curved, and circular or semicircular bundle texture. In addition, zone C has much void space and curvilinear and linear lattice-fringe images with numerous defects, including edge dislocations. Such morphologic and crystallographic characteristics indicate that zones B and C probably comprise the glauconitic minerals of the vermicular glaucony grains, and that zone A comprises non-glauconitic micaceous minerals of higher structural order. Zone B is sharply demarcated from zone A, but B zone bundle textures merge gradationally to those of zone C. These spatial relationships suggest that zone B forms first on the surface of zone A. Sub-parallel orientation in the B zone could be produced by initial confinement between adjacent A zones. Once constraints change or are removed, the randomly oriented, curved, and semicircular or circular bundles of zone C develop.

The sedimentation behavior of a fine kaolinite, comprising a substantial proportion of colloidal particles as well as non-colloidal ones, has been studied when fresh FeCl3 or F2(SO4)3 electrolytes are added. The sedimentation behavior depends on the pH and the nature of electrolytes and can be explained qualitatively, in our study, by the theory of Derjaguin, Landau, Verwey, and Overbeek (DLVO theory). Fe helps also to aggregate the kaolinite particles in flocs. Two extreme kinds of qualitative sedimentation have been observed: flocculation-sedimentation and accumulation-sedimentation. However, the transition between the two kinds of sedimentation is quite progressive. The present results are discussed in reference to the DLVO theory and the hydrolysis behavior of Fe electrolytes.

The colloidal state (stable, coagulated, or gel-like) and the rheological properties of Na-rich montmorillonite (Wyoming) dispersions are strongly influenced by organic cations. This effect is shown for homologous organic cations: alkyl trimethylammonium ions, paraquat, diquat, alkyl bispyridinium ions, and the triphenylmethane dyes crystal violet, methyl green, and tris (tri-methylammonium phenyl) methane chloride. The critical coagulation concentrations, cK, are small (often < 1 mmol/L) because the cations are enriched in the Stern layer and influence the solvent structure near the surface. The strong adsorption of the counterions at the clay-mineral surface causes cK values to increase with the solid content. Charge reversal (recharging) of the particles was observed with the longer chain alkyl trimethyl-ammonium ions, dodecyl bispyridinium ions, and crystal violet. Other cations reduced the electrophoretic mobility to zero but positive particle charges were not observed.

The plastic viscosity increased sharply at the critical coagulation concentration and showed a minimum slightly below cK, which was caused by the electroviscous effect. Yield values were developed at concentrations above cK. In most cases, yield values reached a plateau where the amount of organic cations was ∼0.5 mmol/g, i.e., about half of the cation-exchange capacity. The cK values decreased with increasing hydrophobicity of homologous compounds, but the yield value showed maxima at intermediate chain lengths. The yield value of several 0.5% dispersions was high, e.g., dodecyl trimethylammonium ions, 71 Pa; paraquat, 100 Pa; diquat, 42 Pa; hexyl bispyridinium ions, 53 Pa (vs. Ca2+, 0.2 Pa; Al3+, 0.7 Pa). The storage modulus as a function of the number of organic cations changed in a similar way as the yield value, and high values were observed (e.g., dodecyl trimethylammonium ions, hexyl bispyridinium ions: 1000 Pa, paraquat: >4000 Pa). Thus, dispersions with high viscosity, yield value, and pronounced viscoelasticity are obtained by coagulating Na-rich montmorillonite dispersions with organic cations.

I was a delicate child, and to my great embarrassment I was excused from gymnastics as a teenager owing to an illness whose identity is still mystery, at least to me. That is when I acquired my world-weariness, a permanent and invincible lethargy that was to get worse with the passing years. Tiredness as a natural state has for many years been a recurring theme, when I'm complaining about life in letters and conversation. My friends consider it a bad habit of mine, almost an attempt to attract attention, and they don't take me seriously. “I'm increasingly falling apart”, I recently told an old friend. He replied with a slightly mocking air: “You've been telling me that for twenty years”. But the truth is - and it is difficult to explain this to anyone younger - that the descent into the void is long, much longer than I would have ever imagined, and slow, so slow as to appear almost imperceptible (although not to me). The descent is continuous and, what is worse, irreversible: you descend one step at a time, but having put your foot on the lower step, you know that you will never return to the higher one. I have no idea how many more downward steps are to follow. I can only be sure that their number is steadily decreasing.

Solutions containing hydroxy-FeAl oligocations (HFA) were prepared by two procedures: (1) treatment of a mixture of FeCl3 and AlCl3 with aqueous Na2CO3, followed by aging of the product and (2) preliminary preparation and aging of hydroxy-Al13 oligocations followed by reaction of the latter with aqueous FeCl3. Ion-exchange of Na-montmorillonite with HFA yield pillared clay (designated as FeAl-PILC) with d(001) values of 1.98–1.56 nm and a surface area of 230 m2/g. The pillar structure, thermal stability, surface acidity, and reduction behavior of the pillared clays were determined by 27Al-NMR, XRD, DTA, Mössbauer spectroscopy, Py-IR, TPD, TPR. Fe/Al ratios greatly affect the pillar structure, surface area and thermal stability of FeAl-PILC. The pillar in FeAl-PILC with Fe/Al ratio <0.5 has a Keggin structure, similar to that of Al-PILC, but the pillar structures of FeAl-PILC with Fe/Al ≥0.5 are the ferric tripolymer species similar to those of Fe-PILC. The basal spacings, surface area, and thermal stability are decreased with increasing Fe/Al ratio. There is relatively strong interaction between Fe and Al in the pillars. The interaction is enhanced with decreasing Fe/Al ratio. Reduction of the Fe phase in FeAl-PILC was reduced by the interaction of Fe with Al.