Quantum random walk of two photons in separable and entangled state

We discuss quantum random walk of two photons using linear optical elements. We analyze the quantum random walk using photons in a variety of quantum states including entangled states. We find that for photons initially in separable Fock states, the final state is entangled. For polarization entangled photons produced by type II downconverter, we calculate the joint probability of detecting two photons at a given site. We show the remarkable dependence of the two photon detection probability on the quantum nature of the state. In order to understand the quantum random walk, we present exact analytical results for small number of steps like five. We present in details numerical results for a number of cases and supplement the numerical results with asymptotic analytical results

Spatial-temporal evolution of the current filamentation instability

The spatial-temporal evolution of the purely transverse current filamentation instability is analyzed by deriving a single partial differential equation for the instability and obtaining the analytical solutions for the spatially and temporally growing current filament mode. When the beam front always encounters fresh plasma, our analysis shows that the instability grows spatially from the beam front to the back up to a certain critical beam length; then the instability acquires a purely temporal growth. This critical beam length increases linearly with time and in the non-relativistic regime it is proportional to the beam velocity. In the relativistic regime the critical length is inversely proportional to the cube of the beam Lorentz factor $\gamma_{0b}$. Thus, in the ultra-relativistic regime the instability immediately acquires a purely temporal growth all over the beam. The analytical results are in good agreement with multidimensional particle-in-cell simulations performed with OSIRIS. Relevance of current study to recent and future experiments on fireball beams is also addressed

Solving quantum master equations in phase space by continued-fraction methods

Inspired on the continued-fraction technique to solve the classical Fokker--Planck equation, we develop continued-fraction methods to solve quantum master equations in phase space (Wigner representation of the density matrix). The approach allows to study several classes of nonlinear quantum systems subjected to environmental effects (fluctuations and dissipation), with the only limitations that the starting master equations may have. We illustrate the method with the canonical problem of quantum Brownian motion in periodic potentials.Comment: 7 pages, 3 figure

Magnetically assisted self-injection and radiation generation for plasma based acceleration

It is shown through analytical modeling and numerical simulations that external magnetic fields can relax the self-trapping thresholds in plasma based accelerators. In addition, the transverse location where self-trapping occurs can be selected by adequate choice of the spatial profile of the external magnetic field. We also find that magnetic-field assisted self-injection can lead to the emission of betatron radiation at well defined frequencies. This controlled injection technique could be explored using state-of-the-art magnetic fields in current/next generation plasma/laser wakefield accelerator experiments.Comment: 7 pages, 4 figures, accepted for publication in Plasma Physics and Controlled Fusio

Dynamin-related protein 1 is required for normal mitochondrial bioenergetic and synaptic function in CA1 hippocampal neurons.

Disrupting particular mitochondrial fission and fusion proteins leads to the death of specific neuronal populations; however, the normal functions of mitochondrial fission in neurons are poorly understood, especially in vivo, which limits the understanding of mitochondrial changes in disease. Altered activity of the central mitochondrial fission protein dynamin-related protein 1 (Drp1) may contribute to the pathophysiology of several neurologic diseases. To study Drp1 in a neuronal population affected by Alzheimer's disease (AD), stroke, and seizure disorders, we postnatally deleted Drp1 from CA1 and other forebrain neurons in mice (CamKII-Cre, Drp1lox/lox (Drp1cKO)). Although most CA1 neurons survived for more than 1 year, their synaptic transmission was impaired, and Drp1cKO mice had impaired memory. In Drp1cKO cell bodies, we observed marked mitochondrial swelling but no change in the number of mitochondria in individual synaptic terminals. Using ATP FRET sensors, we found that cultured neurons lacking Drp1 (Drp1KO) could not maintain normal levels of mitochondrial-derived ATP when energy consumption was increased by neural activity. These deficits occurred specifically at the nerve terminal, but not the cell body, and were sufficient to impair synaptic vesicle cycling. Although Drp1KO increased the distance between axonal mitochondria, mitochondrial-derived ATP still decreased similarly in Drp1KO boutons with and without mitochondria. This indicates that mitochondrial-derived ATP is rapidly dispersed in Drp1KO axons, and that the deficits in axonal bioenergetics and function are not caused by regional energy gradients. Instead, loss of Drp1 compromises the intrinsic bioenergetic function of axonal mitochondria, thus revealing a mechanism by which disrupting mitochondrial dynamics can cause dysfunction of axons

Radar Cross Section Studies/Compact Range Research

A summary is given of the achievements of NASA Grant NsG-1613 by Ohio State University from May 1, 1987 to April 30, 1988. The major topics covered are as follows: (1) electromagnetic scattering analysis; (2) indoor scattering measurement systems; (3) RCS control; (4) waveform processing techniques; (5) material scattering and design studies; (6) design and evaluation of design studies; and (7) antenna studies. Major progress has been made in each of these areas as verified by the numerous publications produced

Analytical pair correlations in ideal quantum gases: Temperature-dependent bunching and antibunching

The fluctuation-dissipation theorem together with the exact density response spectrum for ideal quantum gases has been utilized to yield a new expression for the static structure factor, which we use to derive exact analytical expressions for the temperature{dependent pair distribution function g(r) of the ideal gases. The plots of bosonic and fermionic g(r) display "Bose pile" and "Fermi hole" typically akin to bunching and antibunching as observed experimentally for ultracold atomic gases. The behavior of spin-scaled pair correlation for fermions is almost featureless but bosons show a rich structure including long-range correlations near T_c. The coherent state at T=0 shows no correlation at all, just like single-mode lasers. The depicted decreasing trend in correlation with decrease in temperature for T < T_c should be observable in accurate experiments.Comment: 8 pages, 1 figure, minor revisio

Loss of α-Synuclein Does Not Affect Mitochondrial Bioenergetics in Rodent Neurons.

Increased α-synuclein (αsyn) and mitochondrial dysfunction play central roles in the pathogenesis of Parkinson's disease (PD), and lowering αsyn is under intensive investigation as a therapeutic strategy for PD. Increased αsyn levels disrupt mitochondria and impair respiration, while reduced αsyn protects against mitochondrial toxins, suggesting that interactions between αsyn and mitochondria influences the pathologic and physiologic functions of αsyn. However, we do not know if αsyn affects normal mitochondrial function or if lowering αsyn levels impacts bioenergetic function, especially at the nerve terminal where αsyn is enriched. To determine if αsyn is required for normal mitochondrial function in neurons, we comprehensively evaluated how lowering αsyn affects mitochondrial function. We found that αsyn knockout (KO) does not affect the respiration of cultured hippocampal neurons or cortical and dopaminergic synaptosomes, and that neither loss of αsyn nor all three (α, β and γ) syn isoforms decreased mitochondria-derived ATP levels at the synapse. Similarly, neither αsyn KO nor knockdown altered the capacity of synaptic mitochondria to meet the energy requirements of synaptic vesicle cycling or influenced the localization of mitochondria to dopamine (DA) synapses in vivo. Finally, αsyn KO did not affect overall energy metabolism in mice assessed with a Comprehensive Lab Animal Monitoring System. These studies suggest either that αsyn has little or no significant physiological effect on mitochondrial bioenergetic function, or that any such functions are fully compensated for when lost. These results implicate that αsyn levels can be reduced in neurons without impairing (or improving) mitochondrial bioenergetics or distribution