Evidence for the helicity barrier from measurements of the turbulence transition range in the solar wind

The means by which the turbulent cascade of energy is dissipated in the solar wind, and in other astrophysical systems, is a major open question. It has recently been proposed that a barrier to the transfer of energy can develop at small scales, which can enable heating through ion-cyclotron resonance, under conditions applicable to regions of the solar wind. Such a scenario fundamentally diverges from the standard picture of turbulence, where the energy cascade proceeds unimpeded until it is dissipated. Here, using data from NASA's Parker Solar Probe, we find that the shape of the magnetic energy spectrum around the ion gyroradius varies with solar wind parameters in a manner consistent with the presence of such a barrier. This allows us to identify critical values of some of the parameters necessary for the barrier to form; we show that the barrier appears fully developed for ion plasma beta of below $\simeq0.5$ and becomes increasingly prominent with imbalance for normalised cross helicity values greater than $\simeq0.4$. As these conditions are frequently met in the solar wind, particularly close to the Sun, our results suggest that the barrier is likely playing a significant role in turbulent dissipation in the solar wind and so is an important mechanism in explaining its heating and acceleration

Analysis of the Peptidoglycan Hydrolase Complement of Lactobacillus casei and Characterization of the Major γ-D-Glutamyl-L-Lysyl-Endopeptidase

Peptidoglycan (PG) is the major component of Gram positive bacteria cell wall and is essential for bacterial integrity and shape. Bacteria synthesize PG hydrolases (PGHs) which are able to cleave bonds in their own PG and play major roles in PG remodelling required for bacterial growth and division. Our aim was to identify the main PGHs in Lactobacillus casei BL23, a lactic acid bacterium with probiotic properties

Analyse des signaux pour un dispositif de mesure et de stimulation du système nerveux central

- Un des enjeux actuels en Neurosciences est de pouvoir enregistrer simultanément les activités d'un grand nombre de cellules au sein de grands réseaux de neurones, et de pouvoir stimuler de manière dynamique ces réseaux afin d'en contrôler les activités. Le but du projet Neurocom est de réaliser un système multiélectrode haute densité intégré sur silicium, permettant d'enregistrer et de stimuler de grands réseaux de neurones in vitro. Ce dispositif sera constitué d'une microstructure d'électrodes stérilisable hybridée sur un circuit analogique intégré (préamplification, filtrage, multiplexage, stimulation), lui-même interfacé via une carte numérique de commande et acquisition reliée à un PC. Afin de pouvoir mieux appréhender les phénomènes bioélectriques et électrochimiques à l'interface capteur et donc mieux spécifier le cahier des charges et l'architecture du système, la maquette de test NEUROCOM1 a été conçue en électronique discrète et est actuellement utilisée pour conduire différents tests

Matching neural and muscle oscillators: control by FMRFamide-like peptides

Stomatogastric nervous systems of the shrimp, Palaemon serratus, were stained with antisera raised against the peptide FMRFamide. FMRFamide- like immunoreactivity was found in fibers in the input nerve to the stomatogastric ganglion (STG), in several STG somata, in dense neuropil in the STG, in the motor nerves that innervate the dilator muscles of the pyloric region, but not in the pyloric dilator (PD) motor neurons. FMRFamide and several FMRFamide-like peptides elicited sequences of rhythmic depolarizations and contractions of the pyloric dilator muscle. As peptide concentrations were increased, a discrete threshold for contraction was found, above which contractions were initiated with a decreasing latency in an all-or-none fashion. Muscles stopped rhythmically contracting after many seconds to several minutes of activity; the duration of spontaneous oscillatory activity in peptide was proportional to the concentration of applied peptide. In the absence of peptide, each motor neuron discharge evoked small graded muscle contractions. During peptide-induced oscillations, motor neuron activity did not always entrain muscle oscillations. After spontaneous oscillations had stopped, when the motor neurons were stimulated in the presence of the peptide, each motor neuron burst evoked large amplitude contractions as a result of the peptide-induced regenerative properties of the muscle membrane.</jats:p