Strain localization in sandstone during embryonic stages of shear-zone evolution

Geometric analysis of nested Riedel structures was used to identify and quantify strain localization processes within faulted Navajo sandstone. The analysis shows systematic deviation from the basic Riedel geometry complying with the Mohr–Coulomb criterion. Using cross-cutting relations amongst deformation bands within the Riedel structures, and comparing the orientations of the deformation bands to theoretical strain calculations, we identify two coupling deformation mechanisms involved in the early stages of shear-zone evolution, namely, granular flow and discrete faulting. Both mechanisms localize during strain accumulation, and the granular flow facilitates considerable change in the initial geometry of the Riedel structures. The analysis demonstrates a systematic sequence, by which new Riedel structures form after a constant amount of shear strain takes place in the sandstone. Analysis further indicates that granular flow is the major deformation mechanism during early stages of shear-zone evolution and discrete faulting is the dominant mechanism during later deformation stages.     

Cosmic-ray propagation in compressible turbulent media

The influence of compressibility of media on both the statistical acceleration and the turbulent diffusion of cosmic-ray particles is investigated. The averaging over an ensemble of random velocity fields of the medium was performed in the kinetic equation. The kinetic coefficients, which are responsible for the particle acceleration, were obtained in the cases of weak and strong scattering due inhomogeneous magnetic fields.     

Diffusion of seawater ions. Part II. The role of activity coefficients and ion pairing

A theoretical evaluation of basic thermodynamic relationships reveals that variation of activity coefficients, ion pairing and electrical interactions must be considered when modelling ionic diffusion in seawater. The contributions of ion-pair formation and change in activity coefficient along the diffusion path were studied experimentally by conducting diffusion experiments in which solutions of KCl, NaCl, MgCl₂, Li₂SO₄, K₂SO₄, Na₂SO₄ and MgSO₄, at an ionic strength of 0.7, were allowed to diffuse into distilled water. The study reveals that the thermodynamic factor, required to correct for changes in the activity coefficient along the diffusion path, is significant for all the salts studied. Agreement between a simple diffusion model, which does not include ion pairing, and observed data was good for completely dissociated salts, but poor for salts which are known to form ion pairs at the concentration levels studied. The diffusion of MgSO₄, 0.425 of which is associated at I = 0.7, was successfully modelled by assuming that the diffusion coefficient of the MgSO₄⁰ ion pair is different from the diffusion coefficient of the dissociated salt. The diffusion coefficient of this ion pair is estimated to be 1.9 × 10⁻⁵ cm² s⁻¹ at 30°C, as compared to 0.49 × 10⁻⁵ cm² s⁻¹ for the dissociated salt. It is suggested that the high mobility of this ion pair could cause magnesium enrichment in pore water of sulfate depleted sediments.     

Effects of benzene and dimethylnaphthalene on homeostatic processes in two species of crabs

Long-term exposure of animals to sub-lethal doses of toxicants such as benzene (B) and dimethylnaphthalene (DMN) may result in subtle changes in their physiology and biochemistry. In crustaceans such changes include decreased rate of limb regeneration, extended time to molt and decreased growth increment at molt.^1,2 These processes depend upon an adequate supply of stored nutrients in the tissues and appropriate release of neuroendocrine substances from the central nervous system.^3,4 We are examining the effects of sub-lethal doses of B and DMN on osmotic and ionic regulation and on nutrient storage in the blue crab, Callinectes sapidus, and the green crab, Carcinus maenas. Disturbances in these physiological processes may reflect alterations in neuroendocrine functions brought about by the presence of toxicants. We find that exposure of C. maenas to B or DMN, followed by transfer to a dilute medium, results in impaired osmoregulatory capacity, while addition of these compounds to a dilute medium to which the animal is already acclimated does not affect their regulatory ability. Storage of carbohydrate in the midgut gland (hepatopancreas) is decreased by B or DMN, while the accessory storage tissues (gill, muscle) are not significantly affected.     

Pressure-temperature conditions in the Wadi Kid metamorphic complex: Implications for the pan-african event in SE Sinai

Geothermobarometry using continuous equilibria in pelitic rocks of the central and northeastern Wadi Kid areas, Sinai, yields pressure estimates of 320 MPa (3.2 kbar) and temperature estimates of 565° C and >620° C for staurolite-andalusite zone assemblages and anatectic rocks, respectively. This corresponds to geothermal gradients of 47° C/km and 50° C/km. TheseP-T conditions are shown to be compatible with burial under a volcanic cover. The principal heat source for high-grade metamorphism and anatexis is thought to be rising magmatic diapirs. Uplift was relatively slow and the final stages of heating and early stages of cooling probably occurred isobarically. The data imply a high heat flow regime for the Pan-African event in Sinai.     

Oxygen isotope variations in phosphate of biogenic apatites,I. Fish bone apatite—rechecking the rules of the game

The major advantage of the oxygen in phosphate isotope paleothermometry is that it is a system which records temperatures with great sensitivity while bone (and teeth) building organisms are alive, and the record is nearly perfectly preserved after death. Fish from seven water bodies of different temperatures (3–23°C) and different δ¹⁸O (values ?16 to +3) of the water were analysed. The δ¹⁸O values of the analysed PO₄ vary from 6 to 25. The system passed the following tests: (a) the temperatures deduced from isotopic analyses of the sequence of fish from Lake Baikal are in good agreement with the temperatures measured in the thermally stratified lake; (b) the isotopic composition of fish bone phosphate is not influenced by the isotopic composition of the phosphate which is fed to the fish, but only by temperature and water composition.Isotopic analysis of fossil fish in combination with analysis of mammal bones should be a useful tool in deciphering continental paleoclimates.     

The interaction of magnesium with calcite during crystal growth at 25–90°C and one atmosphere

Calcite crystals were grown in a closed system by recrystallization of synthetic and natural aragonite crystals, in the presence of various CaCl2-MgCl2 solutions with and without NaCl.The distribution of Mg2+ between calcite and solution at the entire temperature range is heterogeneous, closely following the Doerner-Hoskins (Doerner and Hoskins, 1925) distribution law. λMg2+C is strongly dependent on temperature, being: 0·0573 ± 0·0017 at 25°C, 0·0681 ± 0·0019 at 35°C, 0·0778 ± 0.0022 at 50°C, 0·0973 ± 0·0021 at 70°C, and 0·1163 ±0 ·0034 at 90°C. λMg2+C is independent of the absolute concentration of Ca2+ in solution as well as of the presence of NaCl.Relatively high λMg2+C values are obtained during the initial reaction stages when too-highly reactive synthetic aragonites are recrystallized. SEM micrographs show that calcite crystals grown from such aragonites are imperfect and that their earlier formed Mg-rich cores redissolve later, resulting in apparently inconsistent λMg2+C values.Calculations applying the new λMg2+C value for 25°C and the solubility data for magnesian calcites (Chaveet al., 1962) demonstrate that although no calcite should be expected to precipate directly from open sea water, its direct precipitation (or recrystallization from aragonite) is possible in closed diagenetic systems which still contain marine solutions, provided a temporary increase in the dissolved calcium concentration takes place.The λMg2+C values obtained allow for a new insight into processes of calcite cementation of reefs and a variety of other carbonate sediments, and for a more precise definition of dedolomitization chemistry.