Bifrontal transcranial direct current stimulation slows reaction time in a working memory task

Background  

Weak transcortical direct current stimulation (tDCS) applied to the cortex can shift the membrane potential of superficial neurons thereby modulating cortical excitability and activity. Here we test the possibility of modifying ongoing activity associated with working memory by tDCS. The concept of working memory applies to a system that is capable of transiently storing and manipulating information, as an integral part of the human memory system. We applied anodal and cathodal transcranial direct current (tDCS) stimulation (260 μA) bilaterally at fronto-cortical electrode sites on the scalp over 15 min repeatedly (15 sec-on/15 sec-off) as well as sham-tDCS while subjects performed a modified Sternberg task.     

Fluctuation spectrum of fluid membranes coupled to an elastic meshwork: jump of the effective surface tension at the mesh size

We identify a class of composite membranes: fluid bilayers coupled to an elastic meshwork that are such that the meshwork's energy is a function F(el)[A(xi)] not of the real microscopic membrane area A, but of a smoothed membrane's area A(xi), which corresponds to the area of the membrane coarse grained at the mesh size xi. We show that the meshwork modifies the membrane tension sigma both below and above the scale xi, inducing a steep crossover of amplitude deltasigma=dF(el)/dA(xi). The predictions of our model account for the fluctuation spectrum of red blood cell membranes coupled to their cytoskeleton. Our results indicate that the cytoskeleton might be under extensional stress, which would provide a means to regulate available membrane areas. We also predict an observable tension jump for membranes decorated with polymer "brushes."     

Taking advantage of multiple scattering to communicate with time-reversal antennas

We present an experimental demonstration showing that, contrary to first intuition, the more scattering a mesoscopic medium is, the more information can be conveyed through it. We used a multiple input-multiple output configuration: a multichannel ultrasonic time-reversal antenna is used to transmit random series of bits simultaneously to different receivers which were only a few wavelengths apart. Whereas the transmission is free of error when multiple scattering occurs in the propagation medium, the error rate is huge in a homogeneous medium.     

A tetranuclear Cr(III)Ni(II)3 cyano-bridged complex based on M(tacn) derivative building blocks

The reaction of Cr(Bztacn)(CN)3 (Bztacn is 1,4,7-trisbenzyl-1,4,7-triazacyclononane) with Ni(iPrtacn)Cl2 (iPrtacn is 1,4,7-trisisopropyl-1,4,7-triazacyclononane) affords a CrNi3 tetranuclear complex. Variable temperature and magnetization versus field measurements show a S = 9/2 ground state and an appreciable magnetic anisotropy with a negative D(9/2) value equal to -0.54 cm(-1). Magnetization studies on one single crystal using a micro-SQUID show a fast tunneling process at zero field at very low temperature.     

Fourier transform infrared characterization of the azido complex of methane monooxygenase hydroxylase from Methylococcus capsulatus (Bath)

The azido complex formed in oxidized methane monooxygenase from Methylococcus capsulatus (Bath) was investigated with resonance Raman and FTIR techniques. These experiments show the presence of a nuas(NNN) at approximately 2077 cm-1 which splits to two components at 2059 and 2073 cm-1 with 15N14N2. The vibrational data are assigned to an azido complex bound terminally to one iron(III) at the diiron center. When the azido complex is illuminated at 15 K, a new nuas(NNN) is observed at 2136 cm-1 which is assigned to a photodissociated HN3 within the substrate pocket. We propose a model where an aqua ligand engages a hydrogen bond interaction with the 1N atom of the azido group and acts as at a proton donor during the photolysis process.     

Reactivity of titanium oxo ethoxo cluster [Ti16O16(OEt)32]. Versatile precursor of nanobuilding block-based hybrid materials

Oxo alcoxo metallic clusters can be employed as inorganic nanobuilding blocks to obtain well-defined organic-inorganic hybrid materials. A better understanding of the surface reactivity of the clusters should allow optimization of the elaboration of hybrid materials through a better control of the hybrid interface. The oxo alcoxo cluster Ti(16)O(16)(OEt)32 presents a shell of labile ethoxy groups that can be selectively transalcoholyzed with preservation of the titanium oxo core, leading to new oxo alcoxo clusters Ti(16)O(16)(OEt)32-x(OR)x (R: alkyl, phenyl, styrenic, etc. groups). The reactivity of the Ti(16)O(16)(OEt)32 cluster toward aliphatic and aromatic alcohols is investigated to determine both the kinetics and the number of substituted titanium atoms, which are strongly dependent on the nature of the alcohol. Characterization of the organic modification of the cluster is performed in situ by liquid (13)C NMR measurements, using the molecular structures of two new clusters, Ti(16)O(16)(OEt)28(OnPr)4 and Ti(16)O(16)(OEt)(24)(OnPr)(8) (OnPr = propoxy groups), as references. The structures of these clusters have been established using single-crystal X-ray diffraction. Moreover, a complete spectroscopic assignment of each ethoxy group is proposed after combining crystallographic data, (13)C NMR T(1) relaxation measurements, and (1)H-(1)H, (1)H-(13)C 2D NMR experiments. Finally, the cluster is functionalized with polymerizable ligands via transalcoholysis and transesterification reactions using hydroxystyrene and acetoxystyrene.     

Duality of Heights Over Quaternion Algebras

Given a number field K, it is well-known that the height of a subspace in K^N and of its orthogonal complement coincide. We prove the analogous fact when K is replaced by a positive definite rational quaternion algebra with respect to the heights recently introduced by the first author. Since quaternion algebras are non-commutative, we cannot just follow the classical proof but have to work with localizations and certain finite rings.     

System-size dependence of strangeness production in nucleus-nucleus collisions at squareroot[sNN]=17.3 GeV

Emission of pi+/-, K+/-, phi, and Lambda was measured in near-central C+C and Si+Si collisions at 158 AGeV beam energy. Together with earlier data for p+p, S+S, and Pb+Pb, the system-size dependence of relative strangeness production in nucleus-nucleus collisions is obtained. Its fast rise and the saturation observed at about 60 participating nucleons can be understood as the onset of the formation of coherent systems of increasing size.     

Three-dimensional modelling of micromachined-ultrasonic-transducer arrays operating in water

We report on the 3-D modelling of periodic arrays of capacitive micromachined ultrasonic transducers (cMUTs) operating in fluid. Specific developments have been performed to model biperiodic transducer arrays and to take into account radiation into any stratified media at the front-side as well as the back-side of the device. The model is based on a periodic finite-element-analysis/boundary-element-method (FEA/BEM). It is applied to micromachined ultrasonic transducers (MUTs), based on silicon-nitride-circular-membrane arrays on a silicon substrate, and operating in water. The spectrum characteristics of MUTs excited in phase are investigated, showing that very-large-band emission is achievable as previously demonstrated by many authors. However, other contributions are also found, depending on the excitation conditions, that do not radiate in the fluid. These contributions are identified as guided modes that could generate significant cross-talk effects. The origin and the nature of these modes is analyzed to gain insight in the actual operation of MUTs.     

Control of adhesion and surface forces via potential-dependent adsorption of pyridine

The orientation and extent of adsorption of pyridine on a gold electrode is known to depend on applied potential and is well characterized. By use of the electrochemical surface forces apparatus, we measured the potential dependence of the double-layer interactions and adhesive forces between a gold electrode and a mica surface for different pyridine concentrations. We observed that, unlike mica-mica interactions, the gold-mica interactions were strongly affected by the presence of small concentrations of pyridine. We are able to reach high negative surface potentials (as determined by applying Derjaguin-Landau-Verway-Overbeek theory to our force measurements), which is similar to what is observed in the absence of pyridine. This demonstrates the electronic nature of the forces measured and shows that pyridine does not displace potential-determining ions on the surface. At positive potentials, where the interaction between gold and mica is attractive, pull-off measurements are a strong function of applied potential. The major effect of the presence of pyridine is on the observed shift in the potential of zero force (PZF), moving it to more negative potentials. This effect is caused by the strong dipole of the pyridine molecule. When the applied potential is cast as a deviation from the PZF, the effect of pyridine is to reduce adhesion between gold and mica. We modeled the potential-dependent adhesion of this system using an electrocapillary framework developed previously, and in doing so, we establish the relationship between the gold-liquid and gold-mica surface energies. In addition, we show that pyridine adsorption affects the capacitance of the gold-mica interface.