Relation entre fabriques de la sanidine et mise en place des magmas trachytiques (exemple de massif de Hradiště, Bohême du nord)

Résumén

La distribution des fabriques dans un dôme trachytique a été analysée sur la base des orientations préférentielles des cristaux de sanidine. L’orientation préférentielle des plans (010) des cristaux de sanidine a été quantifiée par le calcul du tenseur d’orientation. Le sens de cisaillement a été déterminé à l’aide de relations entre les plans S et C.

Les plans (010) des cristaux de sanidine montrent une fabrique résultant d’un aplatissement dans la partie centrale du dôme et d’un cisaillement simple dans les parties marginales. Les critères de cisaillement montrent le mouvement uni forme de magma trachytique à l’échelle de tout le massif. Nous interprétons la disposition des plans S-C et la répartition des fabriques dans le massif à la superposition de lames successives de magma les unes sur les autres. L’acquisition des fabriques dans le massif est comparée aux expériences en compression uniaxiale le Tullis (1976) et la mise en place des magmas trachytiques est assimilée au mouvement d’un piston dans des conditions de basse pression de confinement et de haute vitesse de déformation pendant le stade d’intrusion précuce. Le gonflement faible a modifié tardivement les fabriques initiales surtout dans la partie de déversement et sommitale.     

An Intercomparison Study of the Germanium Isotope Composition of Geological Reference Materials

Recent analytical developments in germanium stable isotope determination by multicollector ICP‐MS have provided new perspectives for the use of Ge isotopes as geochemical tracers. Here, we report the germanium isotope composition of the NIST SRM 3120a elemental reference solution that has been calibrated relative to internal isotopic standard solutions used in the previous studies. We also intercalibrate several geological reference materials as well as geological and meteoritic samples using different techniques, including online hydride generation and a spray chamber for sample introduction to MC‐ICP‐MS, and different approaches for mass bias corrections such as sample–calibrator bracketing, external mass bias correction using Ga isotopes and double‐spike normalisation. All methods yielded relatively similar precisions at around 0.1‰ (2s) for δ^74/70Ge values. Using igneous and mantle‐derived rocks, the bulk silicate Earth (BSE) δ^74/70Ge value was re‐evaluated to be 0.59 ± 0.18‰ (2s) relative to NIST SRM 3120a. Several sulfide samples were also analysed and yielded very negative values, down to ?4.3‰, consistent with recent theoretical study of Ge isotope fractionation. The strong heavy isotope depletion in ore deposits also contrasts with the generally positive Ge isotope values found in many modern and ancient marine sediments.     

Modelling uncertainties in short-term reservoir operation using fuzzy sets and a genetic algorithm / Modélisation d’incertitudes dans la gestion de barrage à court terme grâce à des ensembles flous et à un algorithme génétique

Abstract

Abstract Various uncertainties are inherent in modelling any reservoir operation problem. Two of these are addressed in this study: uncertainty involved in the expression of reservoir penalty functions, and uncertainty in determining the target release value. Fuzzy set theory was used to model these uncertainties where the preferences of the decision maker for the fuzzified parameters are expressed as membership functions. Nonlinear penalty functions are used to determine the penalties due to deviations from targets. The optimization was performed using a genetic algorithm with the objectives to minimize the total penalty and to maximize the level of satisfaction of the decision maker with fuzzified input parameters. The proposed formulation was applied to the problem of finding the optimal release and storage values, taking Green reservoir in Kentucky, USA as a case study. The approach offers more flexibility to reservoir decision-making by demonstrating an efficient way to represent subjective uncertainties, and to deal with non-commensurate objectives under a fuzzy multi-objective environment.     

Mechanical analysis of en echelon structure and its significance of controlling earthquakes

The paper deals with the mechanical origin and rules ofen echelon folds and their secondary fractures by means of elastic stability theory and nonlinear fracture criterion. Obtains the quantitative relations amongen echelon angles ofen echelon folds, ratios of boundary stresses anden echelon pitches of shear zone under an action of general boundary forces (tension shear, pure shear or compression shear). As an applied example, the paper researches the displacement field, stress field, distortion energy distribution, state of secondary fractures and energy released by fracturing ofen echelon fold structure developed at the east foot of Taihang Mountain. The results of research show that maximum principal (compressive) stresses, maximum shear stresses, high value area of distortion energy are in the nuclear parts ofen echelon folds. In these parts compressive fractures were easily developed in approximately parallel with fold axis. So it is verified that the secondary fracture ofen echelon folds is a mechanism controlling a strong earthquake.     

Les auditeurs polonais des cours de minéralogie de René Just Haüy au Muséum national d'Histoire naturelle,Paris

The paper analyses a list of thirty-four Poles, listeners to the mineralogy lectures given by R.-J. Haüy at MNHN in Paris. These students played an important role in the history of Polish Earth Sciences (S. Staszic and F. Drzewiński), but also in other scientific fields (J. Markowski, I. Ab?amowicz, F. Drzewiński, M.A. Paw?owicz, J.K. Skrodzki, E.K. Nowicki), and even in political and cultural life of Poland (A. Downarowicz, J. Weyssenhoff, S. Plater, J. Bieliński, F. Potocki). This paper presents later relations between R.-J. Haüy and his Polish students. A possibility of the Poles' attendance to mineralogy lectures given at other Parisian scientific institutions, like the ‘École des mines’ and the ‘College de France’, is also discussed. To cite this article: R. Tarkowski, P. Daszkiewicz, C. R. Geoscience 338 (2006).     

Experience of the International Association of Geoanalysts as a Certifying Body

Reference materials (RMs) to support geoanalysis have a long history, dating back to the issuance of G-1 and W-1 in 1951. This paper addresses only one aspect of the most recent part of that history, the experience of the International Association of Geoanalysts (IAG) as a certifying body. In 2002, the Certification Committee of the IAG met in Potsdam to discuss becoming a certifying body able to produce RMs for the geoanalytical community. Following that meeting, the IAG developed and published a protocol to assure that IAG RMs would meet International Organization for Standardization (ISO) guidelines to the fullest extent possible. Many practical problems arise in the application of the recommendations of the ISO Guides to any one specific certification project. The recommendations describe the ideal; achievable reality is always somewhat less than that ideal, presenting a significant challenge to the IAG as a certifying body. This paper will summarise experience to date, while focusing on the most challenging issues, deriving uncertainties compliant with the Guide to Uncertainty in Measurement (GUM) and establishing traceability of certified values (CVs).     

Multi-Elemental Analysis of ATHO-G Rhyolitic Glass (MPI-DING Reference Material) by Femtosecond and Nanosecond LA-ICP-MS: Evidence for Significant Heterogeneity of B,V, Zn,Mo, Sn,Sb, Cs,W, Pt and Pb at the Millimetre Scale

This paper reports on the application of variants of LA-ICP-MS – including infrared femtosecond laser ablation (fs-LA) inductively coupled plasma-quadrupole mass spectrometry (ICP-QMS) and nanosecond laser ablation (ns-LA) coupled with single-collector sector-field (SF-) ICP-MS – to the in situ determination of trace elements in different splits of the reference material (RM) ATHO-G (MPI-DING). Analyses of the materials performed by fs- and ns-LA-ICP-MS demonstrated the efficiency of the techniques with typical accuracy at a level of ≤ ± 20%. One ‘anomalous’ split, however, displayed a significant discrepancy from the reference concentrations for B, V, Zn, Mo, Sn, Sb, Cs, W and Pb. Three- to six-fold enrichment of V, Mo, Cs and Pt relative to the reference contents in this split is likely to have been due to direct contact of the silicate melt with Pt crucible walls and ceramics. Boron, Zn, Sn, Sb, W and Pb depletion relative to the reference concentrations is probably due to siderophile element adsorption by the Pt walls and/or related to the formation of volatile-depleted compositional cords during the preparation process. Our results imply that additional precautions should be taken against volatile/siderophile element heterogeneity in marginal/surface layers (≤ 10 mm) during the preparation of RMs by the fusion technique.     

High‐Precision Fe and Mg Isotope Ratios of Silicate Reference Glasses Determined In Situ by Femtosecond LA‐MC‐ICP‐MS and by Solution Nebulisation MC‐ICP‐MS

In this study, a technique for high precision in situ Fe and Mg isotope determinations by femtosecond‐laser ablation‐multi collector‐ICP‐MS (fs‐LA‐MC‐ICP‐MS) was developed. This technique was employed to determine reference values for a series of common reference glasses that may be used for external standardisation of in situ Fe and Mg isotope determinations in silicates. The analysed glasses are part of the MPI‐DING and United States Geological Survey (USGS) reference glass series, consisting of basaltic (BIR‐1G, BCR‐2G, BHVO‐2G, KL2‐G, ML3B‐G) and komatiitic (GOR128‐G and GOR132‐G) compositions. Their Fe and Mg isotope compositions were determined by in situ fs‐LA‐MC‐ICP‐MS and by conventional solution nebulisation multi‐collector ICP‐MS. We determined δ⁵⁶Fe values for these glasses ranging between ‐0.04‰ and 0.10‰ (relative to IRMM‐014) and δ²⁶Mg values ranging between ‐0.40‰ and ‐0.15‰ (relative to DSM‐3). Our fs‐LA‐MC‐ICP‐MS results for both Fe and Mg isotope compositions agreed with solution nebulisation analyses within analytical uncertainties. Furthermore, the results of three USGS reference glasses (BIR‐1G, BHVO‐2G and BCR‐2G) agreed with previous results for powdered and dissolved aliquots of the same reference materials. Measurement reproducibilities of the in situ determinations of δ⁵⁶Fe and δ²⁶Mg values were usually better than 0.12‰ and 0.13‰ (2s), respectively. We further demonstrate that our technique is a suitable tool to resolve isotopic zoning in chemically‐zoned olivine crystals. It may be used for a variety of different applications on isotopically‐zoned minerals, e.g., in magmatic or metamorphic rocks or meteorites, to unravel their formation or cooling rates.