Decrypting magnetic fabrics (AMS, AARM, AIRM) through the analysis of mineral shape fabrics and distribution anisotropy

The fieldwork was supported by the DIPS project (grant no. 240467) and the MIMES project (grant no. 244155) funded by the Norwegian Research Council awarded to O.G. O.P.'s position was funded from Y-TEC.Anisotropy of magnetic susceptibility (AMS) and anisotropy of magnetic remanence (AARM and AIRM) are efficient and versatile techniques to indirectly determine rock fabrics. Yet, deciphering the source of a magnetic fabric remains a crucial and challenging step, notably in the presence of ferrimagnetic phases. Here we use X-ray micro-computed tomography to directly compare mineral shape-preferred orientation and spatial distribution fabrics to AMS, AARM and AIRM fabrics from five hypabyssal trachyandesite samples. Magnetite grains in the trachyandesite are euhedral with a mean aspect ratio of 1.44 (0.24 s.d., long/short axis), and > 50% of the magnetite grains occur in clusters, and they are therefore prone to interact magnetically. Amphibole grains are prolate with magnetite in breakdown rims. We identified three components of the petrofabric that influence the AMS of the analyzed samples: the magnetite and the amphibole shape fabrics and the magnetite spatial distribution. Depending on their relative strength, orientation and shape, these three components interfere either constructively or destructively to produce the AMS fabric. If the three components are coaxial, the result is a relatively strongly anisotropic AMS fabric (P’ = 1.079). If shape fabrics and/or magnetite distribution are non-coaxial, the resulting AMS is weakly anisotropic (P’ = 1.012). This study thus reports quantitative petrofabric data that show the effect of magnetite distribution anisotropy on magnetic fabrics in igneous rocks, which has so far only been predicted by experimental and theoretical models. Our results have first-order implications for the interpretation of petrofabrics using magnetic methods.Publisher PDFPeer reviewe

Resistance to antivitamin K rodenticides: from wild rodents to humans

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Anticoagulant Rodenticides: Resistance and Residues in Norway Rats in France

In the European Union (EU), anticoagulant rodenticides (AR) represent more than 90% of the commercially available products for use against commensal rodents. The only other active ingredients (CO2, chloralose, corn cob) represent minor alternatives. A major issue in the EU is the resistance level of rat and mice populations, as well as potential non-target species exposure. This study presents results of surveys of anticoagulant resistance in Norway rats based on the sequencing of the VKORC1 gene, the major gene involved in AR and an investigation of the presence of AR residues detected in rodents trapped alive in urban and rural areas in order to investigate the potential risk of secondary poisoning of predators and scavengers. For resistance monitoring, rats were either trapped alive in the city of Lyon or its surroundings, or alternatively rat tails were obtained from pest control operators from France. Specific DNA primers were used for DNA sequencing and mutation identifications. AR residues were monitored by LC-MS-MS (for the 8 ARs marketed in Europe), with a limit of quantification of 1.0 µg/kg in liver samples. AR resistance appears to be extremely common (45-70% of all rats tested, depending on the part of France), with the notable exception of downtown Lyon where all rats are susceptible to AR. AR residues are detected in almost 100% of the rats trapped and tested (>200 individuals in/around Lyon). These results show that resistance is common in France, and evidence from neighboring countries suggests that this is an EU-wide problem. More surprising is the fact that all rodents tested contain detectable residues of AR, which could potentially result in secondary poisoning

Anticoagulant Rodenticides: Resistance and Residues in Norway Rats in France

In the European Union (EU), anticoagulant rodenticides (AR) represent more than 90% of the commercially available products for use against commensal rodents. The only other active ingredients (CO2, chloralose, corn cob) represent minor alternatives. A major issue in the EU is the resistance level of rat and mice populations, as well as potential non-target species exposure. This study presents results of surveys of anticoagulant resistance in Norway rats based on the sequencing of the VKORC1 gene, the major gene involved in AR and an investigation of the presence of AR residues detected in rodents trapped alive in urban and rural areas in order to investigate the potential risk of secondary poisoning of predators and scavengers. For resistance monitoring, rats were either trapped alive in the city of Lyon or its surroundings, or alternatively rat tails were obtained from pest control operators from France. Specific DNA primers were used for DNA sequencing and mutation identifications. AR residues were monitored by LC-MS-MS (for the 8 ARs marketed in Europe), with a limit of quantification of 1.0 µg/kg in liver samples. AR resistance appears to be extremely common (45-70% of all rats tested, depending on the part of France), with the notable exception of downtown Lyon where all rats are susceptible to AR. AR residues are detected in almost 100% of the rats trapped and tested (>200 individuals in/around Lyon). These results show that resistance is common in France, and evidence from neighboring countries suggests that this is an EU-wide problem. More surprising is the fact that all rodents tested contain detectable residues of AR, which could potentially result in secondary poisoning

Comparison of the antithrombotic activity of ferulenol and ferprenin, two prenylated coumarins contained in Ferula communis

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VKORC1 mutations detected in patients resistant to vitamin K antagonists are not all associated with a resistant VKOR activity

International audience. Background: The VKORC1 gene codes for the VKORC1 enzyme, which is responsible for the reduction of vitamin K epoxide into vitamin K. VKORC1 enzyme is the target of vitamin K antagonists (VKA). Twenty-eight rare single mutations in the VKORC1 coding sequence have been reported from resistant patients receiving unusually high doses of VKA to achieve therapeutic anticoagulation. Objectives: It has been suggested that these mutations are responsible for the resistant phenotype, while biochemical consequences of these mutations on the VKORC1 enzyme have not yet been evaluated. Therefore, the aim of this study was to investigate the causality of the VKORC1 mutations in the resistance phenotype. Methods: Wild-type VKORC1 and its spontaneous mutants were expressed in Pichia pastoris and susceptibility to VKA was assessed by the in vitro determination of kinetic and inhibition constants. Results and Conclusions: The in vitro analysis revealed that six mutations only (A26P, A41S, V54L, H68Y, I123N and Y139H) were associated with increase in Ki, suggesting their involvement in the resistance phenotype observed in patients. A41S and H68Y led to selective resistance, respectively, to indane-1,3-dione and 4-hydroxycoumarine derivatives. The other mutations did not increase the Ki. Furthermore, 10 mutations (S52L, S52W, W59L, W59R, V66M, V66G, G71A, N77S, N77T and L128R) led to an almost complete loss of activity. These results suggest the existence of other resistance mechanisms

Laser Processing For 3D Junctionless Transistor Fabrication

International audienceTo take fully advantage of Junctionless transistor (JLT) low cost and low temperature feature we investigate a 475°C process to create onto a wafer a thin poly-Si layer on insulator. We fabricated a 13nm doped (Phosphorous, 10 19 at/cm 3) poly-silicon film featuring excellent roughness values (R max = 1.6nm and RMS=0.2nm). Guidelines for grain size optimization with nanosecond (ns) laser annealing are given. 3D monolithic integration; Junction-less transistor; poly-si

ExaNoDe: Combined Integration of Chiplets on Active Interposer with Bare Dice in a Multi-Chip-Module for Heterogeneous and Scalable High Performance Compute Nodes

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Flavin-containing monooxygenase 3 gene polymorphisms in Turkish population

Flavin-containing monooxygenases (FMOs) represent the second most important human monooxygenase system, after cytochrome P450s (CYPs) and catalyze the oxygenation of many chemicals containing nitrogen-, sulphur-, phosphorous-, selenium-and other nucleophilic heteroatoms. FMO3 is the prominent FMO form in adult human liver. For FMO3, both interindividual variability within a single ethnic group and variability between ethnic groups have been reported. In our study, three prevalent functional FMO3 variants (E158K, V257M, and E308G) were genotyped in healthy Turkish people by polymerase chain reaction (PCR)-restriction fragment length polymorphism (RFLP) methods. The frequencies of alleles and haplotypes were compared with those obtained from different populations. It was found that FMO3 158K, 257M and 308G alleles, demonstrate impaired metabolism toward many FMO3 substrates, were observed frequently in Turkish population similar to the other populations. Also, the frequencies of haplotypes were determined based on individual allelic frequencies and it was observed that the most common haplotypes were haplotip EVE and KVE (E158K/V257M/E308G), which together accounted for 80% of all haplotypes. The obtained data from the present study could be useful for further studies assessing sensitivity to therapeutic drugs, environmental toxicants and common disease