Albian extrusion evidences of the Triassic salt and clues of the beginning of the Eocene atlasic phase from the example of the Chitana-Ed Djebs structure (N.Tunisia): Implication in the North African Tethyan margin recorded events, comparisons

In the northern part of Tunisia, close to Testour/Slouguia, new observations and updated biostratigraphy make it possible to highlight the relation between the Triassic saliferous mass and the surrounding Mesozoic beds (T. M.). Near the (T. M.) boundary, the formations observed consist dominantly of Triassic evaporites reworked in the Early and Late Albian deep-water sedimentary deposits. Throughout the studied area, Jurassic rocks are absent. We propose to interpret the Chitana-Ed Djebs structure originally emplaced as gravitational stretch masses in a passive margin in the same way as the salt bodies of widespread salt province in the Gulf of Mexico. A reconstructed schematic position of the Chitana-Ed Djebs salt body displays a scenario of setting of the salt mass on a submarine palaeo-slope. Moreover, the starting clues of the paroxysmal event of the Late Mesozoic tectonic inversion clearly fossilized through the discordance of the Middle Eocene–Early Lutetian limestone on the Albian series.     

Glossary of Analytical and Metrological Terms from the International Vocabulary of Metrology (2008)

The Joint Committee for Guides in Metrology (JCGM) has introduced a revised third edition of the International Vocabulary of Metrology – basic and general concepts and associated terms ( VIM: 2008 ) that replaces the second edition which was published in 1993. This article includes a table containing the terms and definitions that are most relevant to geoanalysis, designed to extend awareness and to promote best practice in the use of this terminology. Comparison is made, where appropriate, with definitions from the earlier 1993 definitions, to demonstrate the way in which thinking in metrological concepts has evolved over this time period.     

In Situ Determination of First‐Row Transition Metal,Ga and Ge Abundances in Geological Materials via Medium‐Resolution LA‐ICP‐MS

An in situ, medium‐resolution LA‐ICP‐MS method was developed to measure the abundances of the first‐row transition metals, Ga and Ge in a suite of geological materials, namely the MPI‐DING reference glasses. The analytical protocol established here hinged on maximising the ablation rate of the ultraviolet (UV) laser system and the sensitivity of the ICP‐MS, as well minimising the production of diatomic oxides and argides, which serve as the dominant sources of isobaric interferences. Non‐spectral matrix effects were accounted for by using multiple external calibrators, including NIST SRM 610 and the USGS basaltic glasses BHVO‐2G, BIR‐1G and BCR‐2G, and utilising ⁴³Ca as an internal standard. Analyses of the MPI‐DING reference glasses, which represent geological matrices ranging from basaltic to rhyolitic in composition, included measurements of concentrations as low as < 10⁰ μg g^?1 and as high as > 10⁴ μg g^?1. The new data reported here were found to statistically correlate with the ‘preferred’ reference values for these materials at the 95% confidence level, though with significantly better precision, typically on the order of ≤ 3% (2s_m). This analytical method may be extended to any matrix‐matched geological sample, particularly oceanic basalts, silicate minerals and meteoritic materials.     

Provisional Elemental Values for IAEA‐Sewage Sludge by Instrumental Neutron Activation Analysis

The International Atomic Energy Agency (IAEA) organised a proficiency test (PT), IAEA‐CU‐2010‐02, for the determination of elements in sewage sludge. The PT sample was analysed by semi‐absolute standardless k₀‐instrumental neutron activation analysis (k₀‐INAA). Results for seven elements (As, Co, Cr, Fe, Hg, Se, Zn) were submitted to the IAEA by our laboratory. All of our results were scored ‘acceptable’ by the ‘result evaluation criteria’ adopted by the IAEA. The same analytical methodology produced quantitative results for twenty‐six additional elements. In total, thirty‐six elements were determined with uncertainty varying from 4 to 11%. This paper presents the provisional mass fractions of twenty‐six additional elements (Ag, Al, Br, Ca, Ce, Cl, Dy, Eu, Ga, Hf, I, K, La, Mg, Mn, Na, Rb, Sb, Sc, Sm, Ta, Tb, Th, V, U, W) not reported by the IAEA. The analytical methodology was discussed with important sources of spectral, nuclear and fission‐product interferences. It was shown that the important components of uncertainties were the k₀ factor, Q₀ factor, detector efficiency, mass and counting statistics. The methodology was validated by analysing the IAEA‐S7 reference material.     

Annual dissolved fluxes from Central Nepal rivers: budget of chemical erosion in the Himalayas

Annual dissolved element fluxes of Himalayan rivers from Central Nepal are calculated using published river discharge and a new set chemical data of rivers, including monsoon sampling. These are used to study the control on chemical erosion of carbonate and silicate over the whole basin. Chemical erosion of carbonate is mainly controlled by the river runoff but it can be limited by the availability of carbonate in limestone-free basin. Chemical erosion of silicate is well correlated to the runoff. However differences between High Himalayan and Lesser Himalayan basins suggest that physical erosion may also play an important control on silicate weathering. To cite this article: C. France-Lanord et al., C. R. Geoscience 335 (2003).     

Ground penetrating radar inversion in 1-D: an approach for the estimation of electrical conductivity, dielectric permittivity and magnetic permeability

This paper presents a method for inverting ground penetrating radargrams in terms of one-dimensional profiles. We resort to a special type of linearization of the damped E-field wave equation to solve the inverse problem. The numerical algorithm for the inversion is iterative and requires the solution of several forward problems, which we evaluate using the matrix propagation approach. Analytical expressions for the derivatives with respect to physical properties are obtained using the self-adjoint Green's function method. We consider three physical properties of materials; namely dielectrical permittivity, magnetic permeability and electrical conductivity. The inverse problem is solved minimizing the quadratic norm of the residuals using quadratic programming optimization. In the iterative process to speed up convergence we use the Levenberg–Mardquardt method. The special type of linearization is based on an integral equation that involves derivatives of the electric field with respect to magnetic permeability, electrical conductivity and dielectric permittivity; this equation is the result of analyzing the implication of the scaling properties of the electromagnetic field. The ground is modeled using thin horizontal layers to approximate general variations of the physical properties. We show that standard synthetic radargrams due to dielectric permittivity contrasts can be matched using electrical conductivity or magnetic permeability variations. The results indicate that it is impossible to differentiate one property from the other using GPR data.     

Silicate‐oxide mineral chemistry of mafic–ultramafic rocks as an indicator of the roots of an island arc: The Chilas Complex,Kohistan (Pakistan)

The Chilas Complex is a major lower crustal component of the Cretaceous Kohistan island arc and one of the largest exposed slices of arc magma chamber in the world. Covering more than 8000 km², it reaches a current tectonic width of around 40 km. It was emplaced at 85 Ma during rifting of the arc soon after the collision of the arc with the Karakoram plate. Over 85% of the Complex comprises homogeneous, olivine‐free gabbronorite and subordinate orthopyroxene–quartz diorite association (MGNA), which contains bodies of up to 30 km² of ultramafic–mafic–anorthositic association (UMAA) rocks. Primary cumulate textures, igneous layering, and sedimentary structures are well preserved in layered parts of the UMAA in spite of pervasive granulite facies metamorphism. Mineral analyses show that the UMAA is characterized by more magnesian and more aluminous pyroxene and more calcic plagioclase than those in the MGNA. High modal abundances of orthopyroxene, magnetite and ilmenite (in MGNA), general Mg–Fe–Al spatial variations, and an MFA plot of whole‐rock analyses suggest a calc‐alkaline origin for the Complex. Projection of the pyroxene compositions on the Wo–En–Fs face is akin to those of pyroxenes from island arcs gabbros. The presence of highly calcic plagioclase and hornblende in UMAA is indicative of hydrous parental arc magma. The complex may be a product of two‐stage partial melting of a rising mantle diaper. The MGNA rocks represent the earlier phase melting, whereas the UMAA magma resulted from the melting of the same source depleted by the extraction of the earlier melt phase. Some of the massive peridotites in the UMAA may either be cumulates or represent metasomatized and remobilized upper mantle. The Chilas Complex shows similarities with many other (supra)subduction‐related mafic–ultramafic complexes worldwide.     

HP–LT Variscan metamorphism in the Cubito-Moura schists (Ossa-Morena Zone, southern Iberia)

Multi-equilibrium thermobarometry shows that low-grade metapelites (Cubito-Moura schists) from the Ossa–Morena Zone underwent HP–LT metamorphism from 340–370 °C at 1.0–0.9 GPa to 400–450 °C at 0.8–0.7 GPa. These HP–LT equilibriums were reached by parageneses including white K mica, chlorite and chloritoid, which define the earliest schistosity (S₁) in these rocks. The main foliation in the schists is a crenulation cleavage (S₂), which developed during decompression from 0.8–0.7 to 0.4–0.3 GPa at increasing temperatures from 400–450 °C to 440–465 °C. Fe³⁺ in chlorite decreased greatly during prograde metamorphism from molar fractions of 0.4 determined in syn-S₁ chlorites down to 0.1 in syn-S₂ chlorites. These new data add to previous findings of eclogites in the Moura schists indicating that a pile of allochtonous rocks situated next to the Beja-Acebuches oceanic amphibolites underwent HP–LT metamorphism during the Variscan orogeny. To cite this article: G. Booth-Rea et al., C. R. Geoscience 338 (2006).     

Variations of U and Sr isotope ratios in Alsace and Luxembourg rain waters: origin and hydrogeochemical implications

Major and trace element concentrations, as well as Sr and U isotope ratios, were measured in rainwater samples collected in three different locations in Alsace (East of France) and Luxembourg: a mid-altitude mountain site (Aubure Environment HydroGeochemical Observatory), an urban site (Strasbourg) and a peri-urban site located in an area of well developed industrial activity (Esch-sur-Alzette in Luxembourg). Results highlight the quite high spatial and temporal variability of the chemical and isotopic characteristics of rainwater at the regional scale. They also suggest a quite systematic contribution of a local component in the chemical composition of rainwater. In urban and peri-urban sites, the local component is certainly linked to human activities, as it is well illustrated in this study with the Esch-sur-Alzette samples. On the other hand, for the Aubure site, i.e. a small forested watershed of mid-altitude mountain, data presented in this study demonstrate the influence of the vegetation on the chemical composition of rainwater for alkali and calc-alkali elements, as well as for the Sr isotope ratios. Such a result questions the reliability of the method classically used to estimate the rainwater contribution on the river chemical budget. In addition, data of the present study confirm the very low content of uranium in rainwater and demonstrate, especially through the U isotope analysis of Aubure rainwater, the negligible effect of rainwater on U budget of river waters. This work thus outlines the property of U to be a geochemical tracer specific of weathering fluxes carried by rivers. To cite this article: F. Chabaux et al., C. R. Geoscience 337 (2005).