Energy estimates for wave equations with time dependent propagation speeds in the Gevrey class

The total energy of the wave equation is conserved with respect to time if the propagation speed is a constant, but this is not true in general for time dependent propagation speeds. Indeed, it is considered in Hirosawa (2007) [3] that the following properties of the propagation speed are crucial for the estimates of the total energy: oscillating speed, difference from the mean, and the smoothness in Cm category. The main purpose of this paper is to derive a benefit of a further smoothness of the propagation speed in the Gevrey class for the energy estimates.     

Spontaneous supersymmetry breaking by large-N matrices

Motivated by supersymmetry breaking in matrix model formulations of superstrings, we present some concrete models, in which the supersymmetry is preserved for any finite N, but gets broken at infinite N, where N is the rank of matrix variables. The models are defined as supersymmetric field theories coupled to some matrix models, and in the induced action obtained after integrating out the matrices, supersymmetry is spontaneously broken only when N is infinity. In our models, the large value of N gives a natural explanation for the origin of small parameters appearing in the field theories which trigger the supersymmetry breaking.     

Evidence for an energy scale for quasiparticle dispersion in Bi2Sr2CaCu2O8

Quasiparticle dispersion in Bi2Sr2CaCu2O8 is investigated with improved angular resolution as a function of temperature and doping. Unlike the linear dispersion predicted by the band calculation, the data show a sharp break in dispersion at 50+/-15 meV binding energy where the velocity changes by a factor of 2 or more. This change provides an energy scale in the quasiparticle self-energy. This break in dispersion is evident at and away from the d-wave node line, but the magnitude of the dispersion change decreases with temperature and with increasing doping.     

Molecular scale imaging of F-actin assemblies immobilized on a photopolymer surface

A photo-immobilization based process is presented for direct imaging of hierarchical assemblies of biopolymers using atomic force microscopy (AFM). The technique was used to investigate the phase behavior of F-actin aggregates as a function of concentration of the divalent cation Mg2+. The data provided direct experimental evidence of a coil-on-coil (braided) structure of F-actin bundles formed at high Mg2+ concentrations. At intermediate Mg2+ concentrations, the data showed the first images of the two-dimensional nematic rafts discovered by recent x-ray studies and theoretical treatments.