Foreground removal requirements for measuring large-scale CMB B-modes in light of BICEP2

The most convincing confirmation that the B-mode polarization signal detected at degree scales by BICEP2 is due to the Cosmic Microwave Background (CMB) would be the measurement of its large-scale counterpart. We assess the requirements for diffuse component separation accuracy over large portions of the sky in order to measure the large-scale B-mode signal corresponding to a tensor to scalar ratio of r=0.1-0.2. We use the method proposed by Bonaldi & Ricciardi (2011) to forecast the performances of different simulated experiments taking into account noise and foreground removal issues. We do not consider instrumental systematics, and we implicitly assume that they are not the dominant source of error. If this is the case, the confirmation of an r=0.1-0.2 signal is achievable by Planck even for conservative assumptions regarding the accuracy of foreground cleaning. Our forecasts suggest that the combination of this experiment with BICEP2 will lead to an improvement of 25-45% in the constraint on r. A next-generation CMB polarization satellite, represented in this work by the COrE experiment, can reduce dramatically (by almost another order of magnitude) the uncertainty on r. In this case, however, the accuracy of foreground removal becomes critical to fully benefit from the increase in sensitivity.Comment: 8 pages, 3 figures, 1 table. Accepted by MNRA

A stochastic model for the stepwise motion in actomyosin dynamics

A jump-diffusion process is proposed to describe the displacements performed by single myosin heads along actin filaments during the rising phases. The process consists of the superposition of a Wiener and a jump process, with jumps originated by sequences of Poisson-distributed energy-supplying pulses. In a previous paper, the amplitude of the jumps was described by a mixture of two Gaussian distributions. To embody the effects of ATP hydrolysis, we now refine such a model by assuming that the jumps' amplitude is described by a mixture of three Gaussian distributions. This model has been inspired by the experimental data of T. Yanagida and his co-workers concerning observations at single molecule processes level.Comment: 9 pages, 4 figure

A chemically driven fluctuating ratchet model for actomyosin interaction

With reference to the experimental observations by T. Yanagida and his co-workers on actomyosin interaction, a Brownian motor of fluctuating ratchet kind is designed with the aim to describe the interaction between a Myosin II head and a neighboring actin filament. Our motor combines the dynamics of the myosin head with a chemical external system related to the ATP cycle, whose role is to provide the energy supply necessary to bias the motion. Analytical expressions for the duration of the ATP cycle, for the Gibbs free energy and for the net displacement of the myosin head are obtained. Finally, by exploiting a method due to Sekimoto (1997, J. Phys. Soc. Jpn., 66, 1234), a formula is worked out for the amount of energy consumed during the ATP cycle.Comment: 15 pages. 1 figur

Towards the Modeling of Neuronal Firing by Gaussian Processes

This paper focuses on the outline of some computational methods for the approximate solution of the integral equations for the neuronal firing probability density and an algorithm for the generation of sample-paths in order to construct histograms estimating the firing densities. Our results originate from the study of non-Markov stationary Gaussian neuronal models with the aim to determine the neuron's firing probability density function. A parallel algorithm has been implemented in order to simulate large numbers of sample paths of Gaussian processes characterized by damped oscillatory covariances in the presence of time dependent boundaries. The analysis based on the simulation procedure provides an alternative research tool when closed-form results or analytic evaluation of the neuronal firing densities are not available.Comment: 10 pages, 3 figures, to be published in Scientiae Mathematicae Japonica

Biological aspects of mTOR in leukemia

The mammalian target of rapamycin (mTOR) is a central processor of intra-and extracellular signals, regulating many fundamental cellular processes such as metabolism, growth, proliferation, and survival. Strong evidences have indicated that mTOR dysregulation is deeply implicated in leukemogenesis. This has led to growing interest in the development of modulators of its activity for leukemia treatment. This review intends to provide an outline of the principal biological and molecular functions of mTOR. We summarize the current understanding of how mTOR interacts with microRNAs, with components of cell metabolism, and with controllers of apoptotic machinery. Lastly, from a clinical/translational perspective, we recapitulate the therapeutic results in leukemia, obtained by using mTOR inhibitors as single agents and in combination with other compounds

Dispersion of longitudinal momentum distributions induced in fragmentation reactions

On the basis of systematic measurements of fragmentation reactions, which provide a detailed overview on the velocity distributions of residual nuclei, an improved description of the kinematical properties of the fragmentation residues is established. This work is dedicated to the fluctuations of their momentum distributions. In contrast to previous investigations, limited to close-to-projectile fragments, we extended our study to the entire production range, down to the lightest observed fragments. In this context, beside the contribution of abrasion and evaporation processes, we considered the effect of the thermal break-up on the width of the momentum distributions. Using approximated theoretical descriptions of the different reaction stages, a new analytical formula for the variance of the momentum distribution is derived, which is well adapted to technical applications.Comment: 14 pages, 3 figures, background info. at http://www-wnt.gsi.de/charms

On Myosin II dynamics in the presence of external loads

We address the controversial hot question concerning the validity of the loose coupling versus the lever-arm theories in the actomyosin dynamics by re-interpreting and extending the phenomenological washboard potential model proposed by some of us in a previous paper. In this new model a Brownian motion harnessing thermal energy is assumed to co-exist with the deterministic swing of the lever-arm, to yield an excellent fit of the set of data obtained by some of us on the sliding of Myosin II heads on immobilized actin filaments under various load conditions. Our theoretical arguments are complemented by accurate numerical simulations, and the robustness of the model is tested via different choices of parameters and potential profiles.Comment: 6 figures, 8 tables, to appear on Biosystem