Role of inertia in falling head permeability test

This paper discusses the role of macro‐ and micro‐inertial forces in the falling head permeability test. The model of flow including viscous and dynamic interaction forces is formulated. Then, the model is used to perform numerical simulations of the tests for high‐permeability soils. The presented results prove the existence of a level of permeability of materials above which macro‐and micro‐inertial forces are important and that in all cases the latter forces are dominant. The results suggest limited validity of the standard interpretation of the falling head permeability test and possible usefulness of the test to determine both permeability and the parameter characterizing non‐linear interactions of fluid and solid skeleton. Copyright © 2009 John Wiley & Sons, Ltd.     

Hydrodynamic Equilibrium for Sediment Transport and Bed Response to Wave Motion

An experimental and theoretical identification of hydrodynamic equilibrium for sediment transport and bed response to wave motion are considered. The comparison between calculations and the results of laboratory experiments indicates the linear relation between sediment transport rate and the thickness zm of bed layer in which sediments are in apparent rectilinear motion. This linear relationship allows to use the first order “upwind” numerical scheme of FDM ensuring an accurate solution of equation for changes in bed morphology. However, it is necessary to carry out a decomposition of the sediment transport into transport in onshore direction during wave crest and offshore direction during wave trough. Further, the shape of bed erosion in response to sediment transport coincides with the trapezoid envelope or with part of it, when some sediments still remain within it. Bed erosion area is equal to the one of a rectangle with thickness znm.     

Evolution of zircon deformation mechanisms in a shear zone (Lanzo massif,Western-Alps)

Magmatic zircons within two sheared gabbroic dykes from the peridotitic massif of Lanzo (Western-Alps, Italy) revealed evolution of deformation from crystal plasticity to rigid body rotation during shear zone evolution. This is the first time that multiple zircon grains have been analysed in a kinematic context in a shear zone. Zircon grains recorded crystal plastic deformation activating the commonly inferred <100>{001} and <001>{100} glide-systems to the newly identified <001>{110} glide-system. The exact selection of glide-system could be dependant of deformation conditions such as pressure, temperature, and strain rate. Moreover, the activation of one or several glide-systems within a single grain could be favoured by the primary orientation of the grains combined with a high strain rate. In these sheared gabbros, the deformation mechanisms evolve from plastic deformation at low strain rate conditions to increase strain, strain softening and localisation of deformation. The progressive shear zone development and the softening of the matrix relative to the zircon has lead to a switch from crystal-plasticity to rigid body rotation of zircon. The zircon grains rigid body rotation involved that their long axes became parallel to the lineation of the shear zone, causing reorientation and dispersion of the misorientation axes away from kinematic Y.     

Local government, local economic development and quality of life in Poland

The establishment of local self-government was a key part of the post-1989 transformation in East and Central Europe. Local government in both Western and East and Central Europe has increasingly been expected to play a role in local economic development (LED). Local government is one important agent in the complex processes of building 'institutional thickness' to ensure the development of local economies and the quality of life of inhabitants. This paper presents the results of a national postal questionnaire survey of the LED role of the lowest level of local self-government in Poland, the gmina or commune. The paper establishes a baseline of knowledge regarding: the local economic problems faced by communes; their attitudinal, strategic and organisational responses; and the main factors which are hindering the communes' LED role. This revised version was published online in July 2006 with corrections to the Cover Date.     

Direct physical evidence of dolomite recrystallization

The possibility of recrystallization is a long‐standing barrier to deciphering the genetic origin of dolomites. There is often uncertainty regarding whether or not characteristics of ancient dolomites are primary or the consequence of later recrystallization unrelated to the original dolomitization event. Results from 65 new high‐temperature dolomite synthesis experiments (1 m , 1·0 Mg/Ca ratio solutions at 218°C) demonstrate dolomite recrystallization affecting stoichiometry, cation ordering and nanometre‐scale surface texture. The data support a model of dolomitization that proceeds by a series of four unique phases of replacement and recrystallization, which occur by various dissolution–precipitation reactions. During the first phase (induction period), no dolomite forms despite favourable conditions. The second phase (replacement period) occurs when Ca‐rich dolomite products, with a low degree of cation ordering, rapidly replace calcite reactants. During the replacement period, dolomite stoichiometry and the degree of cation ordering remain constant, and all dolomite crystal surfaces are covered by nanometre‐scale growth mounds. The third phase (primary recrystallization period), which occurs in the experiments between 97% and 100% dolomite, is characterized by a reduced replacement rate but concurrent increases in dolomite stoichiometry and cation ordering. The end of the primary recrystallization period is marked by dolomite crystal growth surfaces that are covered by flat, laterally extensive layers. The fourth phase of the reaction (secondary recrystallization period) occurs when all calcite is consumed and is characterized by stoichiometric dolomite with layers as well as a continued increase in the degree of cation ordering with time. Inferences of recrystallization, in natural dolomite, based on cation order or stoichiometry of dolomite, usually depend on assumptions about the precursor dolomite subjected to recrystallization. If it is assumed that the experimental evidence presented here is applicable to natural, low‐temperature dolomites, then the presence of mounds is direct evidence of a lack of recrystallization and the presence of layers is direct evidence of recrystallization.     

High-resolution computed microtomography for the characterization of a diffusion tensor imaging phantom

This paper addresses the issue of the quantitative characterization of the structure of the calibration model (phantom) for b-matrix spatial distribution diffusion tensor imaging (BSD-DTI) scanners. The aim of this study was to verify manufacturing assumptions of the structure of materials, since phantoms are used for BSD-DTI calibration directly after manufacturing. Visualization of the phantoms’ structure was achieved through optical microscopy and high-resolution computed microtomography (µCT). Using µCT images, a numerical model of the materials structure was developed for further quantitative analysis. 3D image characterization was performed to determine crucial structural parameters of the phantom: porosity, uniformity and distribution of equivalent diameter of capillary bundles. Additionally calculations of hypothetical flow streamlines were also performed based on the numerical model that was developed. The results obtained in this study can be used in the calibration of DTI-BST measurements. However, it was found that the structure of the phantom exhibits flaws and discrepancies from the assumed geometry which might affect BSD-DTI calibration.     

Early and pervasive dolomitization by near-normal marine fluids: New lessons from an Eocene evaporative setting in Qatar

The upper Palaeocene–lower Eocene Umm er Radhuma Formation in the subsurface of Qatar is dominated by subtidal carbonate depositional packages overlain by bedded evaporites. In Saudi Arabia and Kuwait, peritidal carbonate depositional sequences with intercalated evaporites and carbonates in Umm er Radhuma have been previously interpreted to have been dolomitized via downward reflux of hypersaline brines. Here, textural, mineralogical and geochemical data from three research cores in Qatar are presented which, in contrast, are more consistent with dolomitization by near-normal marine fluids. Petrographic relationships support a paragenetic sequence whereby dolomitization occurred prior to the formation of all other diagenetic mineral phases, including chert, pyrite, palygorskite, gypsum, calcite and chalcedony, which suggests that dolomitization occurred very early. The dolomites occur as finely crystalline mimetic dolomites, relatively coarse planar-e dolomites, and coarser nonplanar dolomites, all of which are near-stoichiometric (50.3 mol% MgCO₃) and well-ordered (0.73). The dolomite stable isotope values (range −2.5‰ to +1‰; mean δ¹⁸O = −0.52‰) and trace element concentrations (Sr = 40 to 150 ppm and Na = 100 to 600 ppm) are compatible with dolomitization by near-normal seawater or mesohaline fluids. Comparisons between δ¹⁸O values from Umm er Radhuma dolomite and the overlying Rus Formation gypsum further suggest that dolomitization did not occur in fluids related to Rus evaporites. This study provides an example of early dolomitization of evaporite-related carbonates by near-normal seawater rather than by refluxing hypersaline brines from overlying bedded evaporites. Further, it adds to recent work suggesting that dolomitization by near-normal marine fluids in evaporite-associated settings may be more widespread than previously recognized.     

Chemically induced deformation of a porous layer coupled with advective–dispersive transport. Analytical solutions

In this paper a chemically induced deformation of porous material taking place during advective–dispersive transport of a chemical is considered. Linearized governing equations are derived and analytical solutions of 2 one‐dimensional problems for a homogeneous layer with drained boundaries are developed. Numerical results for a particular clayey material and a chemical migrating through the layer showing distributions of concentration of chemical, changes in porosity of the material and pore fluid pressure, and evolution of settlement of the layer as functions of time are discussed. Copyright © 2001 John Wiley & Sons, Ltd.     

Mineralogy,nucleation and growth of dolomite in the laboratory and sedimentary environment: A review

Dolomite [CaMg(CO₃)₂] forms in numerous geological settings, usually as a diagenetic replacement of limestone, and is an important component of petroleum reservoir rocks, rocks hosting base metal deposits and fresh water aquifers. Dolomite is a rhombohedral carbonate with a structure consisting of an ordered arrangement of alternating layers of Ca²⁺ and Mg²⁺ cations interspersed with anion layers normal to the c‐axis. Dolomite has symmetry, lower than the (CaCO₃) symmetry of calcite primarily due to Ca–Mg ordering. High‐magnesium calcite also has symmetry and differs from dolomite in that Ca²⁺ and Mg²⁺ ions are not ordered. High‐magnesium calcite with near‐dolomite stoichiometry (≈50 mol% MgCO₃) has been observed both in nature and in laboratory products and is referred to in the literature as protodolomite or very high‐magnesium calcite. Many dolomites display some degree of cation disorder (Ca²⁺ on Mg²⁺ sites and vice versa), which is detectable using transmission electron microscopy and X‐ray diffractometry. Laboratory syntheses at high temperature and pressure, as well as studies of natural dolomites show that factors affecting dolomite ordering, stoichiometry, nucleation and growth include temperature, alkalinity, pH, concentration of Mg and Ca, Mg to Ca ratio, fluid to rock ratio, mineralogy of the carbonate being replaced, and surface area available for nucleation. In spite of numerous attempts, dolomite has not been synthesized in the laboratory under near‐surface conditions. Examination of published X‐ray diffraction data demonstrates that assertions of dolomite synthesis in the laboratory under near‐ambient conditions by microbial mediation are unsubstantiated. These laboratory products show no evidence of cation ordering and appear to be very high‐magnesium calcite. Elevated‐temperature and elevated‐pressure experiments demonstrate that dolomite nucleation and growth always are preceded by very high‐magnesium calcite formation. It remains to be demonstrated whether microbial‐mediated growth of very high‐magnesium calcite in nature provides a precursor to dolomite nucleation and growth analogous to reaction paths in high‐temperature experiments.