Electron Inertial Effects on Rapid Energy Redistribution at Magnetic X-points

The evolution of non-potential perturbations to a current-free magnetic X-point configuration is studied, taking into account electron inertial effects as well as resistivity. Electron inertia is shown to have a negligible effect on the evolution of the system whenever the collisionless skin depth is less than the resistive scale length. Non-potential magnetic field energy in this resistive MHD limit initially reaches equipartition with flow energy, in accordance with ideal MHD, and is then dissipated extremely rapidly, on an Alfvenic timescale that is essentially independent of Lundquist number. In agreement with resistive MHD results obtained by previous authors, the magnetic field energy and kinetic energy are then observed to decay on a longer timescale and exhibit oscillatory behavior, reflecting the existence of discrete normal modes with finite real frequency. When the collisionless skin depth exceeds the resistive scale length, the system again evolves initially according to ideal MHD. At the end of this ideal phase, the field energy decays typically on an Alfvenic timescale, while the kinetic energy (which is equally partitioned between ions and electrons in this case) is dissipated on the electron collision timescale. The oscillatory decay in the energy observed in the resistive case is absent, but short wavelength structures appear in the field and velocity profiles, suggesting the possibility of particle acceleration in oppositely-directed current channels. The model provides a possible framework for interpreting observations of energy release and particle acceleration on timescales down to less than a second in the impulsive phase of solar flares.Comment: 30 pages, 8 figure

Significance of the E-W fault system in the geodynamic evolution of the Tunisian Alpine Chain foreland. Example of the Sbiba-Cherichira fault system in central Tunisia

En Tunisie centrale, les bassins mio-plio-quaternaires de Sbiba et de Haffouz sont constitués de dépocentres délimités par des failles de direction proche de E-W, NW-SE, N070 o et N-S. Ces accidents bordiers bien identifiés en sub-surface et dont l’activité a été démontrée aux époques éo-crétacées, ont évolué durant le Néogène et le Quaternaire dans un système de décrochements en relais, alliant des structures compressives (plis N040 o à N080 o E, failles inverses, chevauchements…) et des structures distensives correspondant à des grabens et demi-grabens orientés E-W et N120 o à N150 o E. La région a été affectée du Néogène au Quaternaire inférieur par une succession de régimes tectoniques compressifs (liés aux phases tortonienne et villafranchienne) et extensifs (extension post-tectonique oligo-miocène comme dans l’ensemble du Maghreb, mais aussi existence d’une phase d’extension au Miocène terminal-Pléistocène inférieur synchrone du rifting du Bassin tyrrhénien). Cette alternance compression-extension induit plusieurs inversions de subsidence. L’étude tectonique effectuée aux abords de ces décrochements permet non seulement d’apporter des précisions sur l’évolution spatiale des déformations mais aussi d’établir les relations tectono-sédimentaires caractérisant chaque époque du Mio-Plio-Quatemaire : bassins subsidents sur les décrochements, installation de bassins lacustres sur barrages morphostructuraux, variations d’épaisseur et de faciès liées aux failles synsédimentaires

Le carcinome indifférencié des glandes salivaires

Le carcinome indifferencie primitif des glandes salivaires est rare. Son association avec le virus Epstein Barr, initialement decrite chez les esquimaux, est retrouvee dans la majorite des cas publies. Nous rapportons un nouveau cas tunisien survenu chez un homme age de 64 ans, revele par une tumefaction de la glande parotide gauche. Microscopiquement se discutait le caractere primitif ou secondaire de la tumeur, etaye par les examens complementaires. Le patient etait traite par une parotidectomie suivie d’un curage ganglionnaire et d’une radiotherapie. L’evolution etait favorable apres un an de recul.  Mots clès : Glande salivaire- Carcinome indifferencie- Virus Epstein Bar

Genetic Association of rs1021188 and DNA Methylation Signatures of TNFSF11 in the Risk of Conductive Hearing Loss

Otosclerosis (OTSC) is a complex bone disorder of the otic capsule, which causes conductive hearing impairment in human adults. The dysregulation of the signaling axis mediated by the receptor activator of nuclear factor-kappa-B (RANK), RANK ligand (RANKL), and osteoprotegerin has been widely attributed to the context of metabolic bone disorders. While genetic associations and epigenetic alterations in the TNFSF11 gene (RANKL) have been well-linked to metabolic bone diseases of the skeleton, particularly osteoporosis, they have never been addressed in OTSC. This study aimed to assess whether the genetic association of rs1021188 polymorphism in the upstream of TNFSF11 and the DNA methylation changes in its promoter CpG-region reveal the susceptibility of OTSC. Peripheral blood DNA samples were collected from unrelated Tunisian-North African subjects for genotyping (109 cases and 120 controls) and for DNA methylation analysis (40 cases and 40 controls). The gender-stratified analysis showed that the TNFSF11 rs1021188 C/T was associated with OTSC in men (p = 0.023), but not in women (p = 0.458). Individuals with CC genotype were more susceptible to OTSC, suggesting an increased risk to disease development. Using publicly available data, the rs1021188 was within a cluster grouping the subpopulations with African ethnicity. Moreover, 26 loci in the TNFSF11 gene were in linkage disequilibrium with rs1021188, revealing relative similarities between different populations. Significant differences in both DNA methylation and unmethylation status were detected with 4.53- and 4.83-fold decreases in the global DNA methylation levels in female and male OTSC groups, respectively. These changes could contribute to an increased risk of OTSC development. Bioinformatic analyses indicated that each of the rs1021188 variations and the DNA methylation changes in the promoter CpG-sites within TNFSF11 may play an important role in its transcription regulation. To our knowledge, this is the first study that investigates an independent effect of the rs1021188 polymorphism and DNA hypomethylation of TNFSF11 promoter in OTSC. Genetic and epigenetic changes in the regulatory regions of TNFSF11 could offer new molecular insights into the understanding of the complexity of OTSC

Bi-directional Alfv\'en Cyclotron Instabilities in the Mega-Amp Spherical Tokamak

Alfv\'en cyclotron instabilities excited by velocity gradients of energetic beam ions were investigated in MAST experiments with super-Alfv\'enic NBI over a wide range of toroidal magnetic fields from ~0.34 T to ~0.585 T. In MAST discharges with high magnetic field, a discrete spectrum of modes in the sub-cyclotron frequency range is excited toroidally propagating counter to the beam and plasma current (toroidal mode numbers n < 0).Comment: 28 pages, 13 figures. This article has been submitted to Physics of Plasmas. After it is published, it will be found at http://scitation.aip.org/content/aip/journal/pop/brows

Molecular analysis of HBV genotypes and subgenotypes in the Central-East region of Tunisia

<p>Abstract</p> <p>Background</p> <p>In Tunisia, country of intermediate endemicity for Hepatitis B virus (HBV) infection, most molecular studies on the virus have been carried out in the North of the country and little is known about other regions. The aim of this study was to determine HBV genotype and subgenotypes in Central-East Tunisia. A total of 217 HBs antigen positive patients were enrolled and determination of genotype was investigated in 130 patients with detectable HBV DNA. HBV genotyping methods were: PCR-RFLP on the pre-S region, a PCR using type-specific primers in the S region (TSP-PCR) and partial sequencing in the pre-S region.</p> <p>Results</p> <p>Three genotypes (D, B and A) were detected by the PCR-RFLP method and two (D and A) with the TSP-PCR method, the concordance between the two methods was 93%. Sequencing and phylogenetic analysis of 32 strains, retrieved the same genotype (D and A) for samples with concordant results and genotype D for samples with discordant results. The sequences of discordant genotypes had a restriction site in the pre-S gene which led to erroneous result by the PCR-RFLP method. Thus, prevalence of genotype D and A was 96% and 4%, respectively. Phylogenetic analysis showed the predominance of two subgenotypes D1 (55%) and D7 (41%). Only one strain clustered with D3 subgenotype (3%).</p> <p>Conclusions</p> <p>Predominance of subgenotype D7 appears to occur in northern regions of Africa with transition to subgenotype D1 in the East of the continent. HBV genetic variability may lead to wrong results in rapid genotyping methods and sequence analysis is needed to clarify atypical results.</p

Brain MRI and biological diagnosis in five Tunisians MLD patients

Metachromatic leukodystrophy (MLD) is a recessive autosomal disease which is characterized by an accumulation of sulfatides in the central and peripheral nervous system. It is due to the enzyme deficiency of the sulfatide sulfatase i.e. arylsulfatase A (ASA). we studied 5/200 cases of MLD and clearly distinguished three clinical forms. One of them presented the juvenile form; two presented the late infantile form; and two other presented the adult form. The Magnetic Resonance Imaging (MRI) of these patients showed a diffuse, bilateral and symmetrical demyelination. The biochemical diagnosis of MLD patients evidencing the low activity of ASA and sulfatide accumulation

Aerodynamic investigations of ventilated brake discs.

The heat dissipation and performance of a ventilated brake disc strongly depends on the aerodynamic characteristics of the flow through the rotor passages. The aim of this investigation was to provide an improved understanding of ventilated brake rotor flow phenomena, with a view to improving heat dissipation, as well as providing a measurement data set for validation of computational fluid dynamics methods. The flow fields at the exit of four different brake rotor geometries, rotated in free air, were measured using a five-hole pressure probe and a hot-wire anemometry system. The principal measurements were taken using two-component hot-wire techniques and were used to determine mean and unsteady flow characteristics at the exit of the brake rotors. Using phase-locked data processing, it was possible to reveal the spatial and temporal flow variation within individual rotor passages. The effects of disc geometry and rotational speed on the mean flow, passage turbulence intensity, and mass flow were determined. The rotor exit jet and wake flow were clearly observed as characterized by the passage geometry as well as definite regions of high and low turbulence. The aerodynamic flow characteristics were found to be reasonably independent of rotational speed but highly dependent upon rotor geometry

Influence of plasma turbulence on microwave propagation

It is not fully understood how electromagnetic waves propagate through plasma density fluctuations when the size of the fluctuations is comparable with the wavelength of the incident radiation. In this paper, the perturbing effect of a turbulent plasma density layer on a traversing microwave beam is simulated with full-wave simulations. The deterioration of the microwave beam is calculated as a function of the characteristic turbulence structure size, the turbulence amplitude, the depth of the interaction zone and the size of the waist of the incident beam. The maximum scattering is observed for a structure size on the order of half the vacuum wavelength. The scattering and beam broadening was found to increase linearly with the depth of the turbulence layer and quadratically with the fluctuation strength. Consequences for experiments and 3D effects are considered.Comment: 16 pages, 13 figures. This is an author-created, un-copyedited version of an article submitted for publication in Plasma Physics and Controlled Fusion. IoP Publishing Ltd is not responsible for any errors or omissions in this version of the manuscript or any version derived from i