212 research outputs found

    In-plane effects on segmented-mirror control

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    Extremely large optical telescopes are being designed with primary mirrors composed of hundreds of segments. The “out-of-plane” piston, tip, and tilt degrees of freedom of each segment are actively controlled using feedback from relative height measurements between neighboring segments. The “in-plane” segment translations and clocking (rotation) are not actively controlled; however, in-plane motions affect the active control problem in several important ways, and thus need to be considered. We extend earlier analyses by constructing the “full” interaction matrix that relates the height, gap, and shear motion at sensor locations to all six degrees of freedom of segment motion, and use this to consider three effects. First, in-plane segment clocking results in height discontinuities between neighboring segments that can lead to a global control system response. Second, knowledge of the in-plane motion is required both to compensate for this effect and to compensate for sensor installation errors, and thus, we next consider the estimation of in-plane motion and the associated noise propagation characteristics. In-plane motion can be accurately estimated using measurements of the gap between segments, but with one unobservable mode in which every segment clocks by an equal amount. Finally, we examine whether in-plane measurements (gap and/or shear) can be used to estimate out-of-plane segment motion; these measurements can improve the noise multiplier for the “focus-mode” of the segmented-mirror array, which involves pure dihedral angle changes between segments and is not observable with only height measurements

    Soft Covariant Gauges on the Lattice

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    We present an exploratory study of a one-parameter family of covariant, non-perturbative lattice gauge-fixing conditions, that can be implemented through a simple Monte Carlo algorithm. We demonstrate that at the numerical level the procedure is feasible, and as a first application we examine the gauge dependence of the gluon propagator.Comment: 11 pages, Latex, epsf.sty included + 5 PostScript picture

    Current Renormalisation Constants with an O(a)-improved Fermion Action

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    Using chiral Ward identities, we determine the renormalisation constants of bilinear quark operators for the Sheikholeslami-Wohlert action lattice at beta=6.2. The results are obtained with a high degree of accuracy. For the vector current renormalisation constant we obtain Z_V=0.817(2)(8), where the first error is statistical and the second is due to mass dependence of Z_V. This is close to the perturbative value of 0.83. For the axial current renormalisation constant we obtain Z_A = 1.045(+10 -14), significantly higher than the value obtained in perturbation theory. This is shown to reduce the difference between lattice estimates and the experimental values for the pseudoscalar meson decay constants, but a significant discrepancy remains. The ratio of pseudoscalar to scalar renormalisation constants, Z_P/Z_S, is less well determined, but seems to be slightly lower than the perturbative value.Comment: 8 pages uuencoded compressed postscript file. Article to be submitted to Phys.Rev.

    Capping protein modulates the dynamic behavior of actin filaments in response to phosphatidic Acid in Arabidopsis.

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    International audienceRemodeling of actin filament arrays in response to biotic and abiotic stimuli is thought to require precise control over the generation and availability of filament ends. Heterodimeric capping protein (CP) is an abundant filament capper, and its activity is inhibited by membrane signaling phospholipids in vitro. How exactly CP modulates the properties of filament ends in cells and whether its activity is coordinated by phospholipids in vivo is not well understood. By observing directly the dynamic behavior of individual filament ends in the cortical array of living Arabidopsis thaliana epidermal cells, we dissected the contribution of CP to actin organization and dynamics in response to the signaling phospholipid, phosphatidic acid (PA). Here, we examined three cp knockdown mutants and found that reduced CP levels resulted in more dynamic activity at filament ends, and this significantly enhanced filament-filament annealing and filament elongation from free ends. The cp mutants also exhibited more dense actin filament arrays. Treatment of wild-type cells with exogenous PA phenocopied the actin-based defects in cp mutants, with an increase in the density of filament arrays and enhanced annealing frequency. These cytoskeletal responses to exogenous PA were completely abrogated in cp mutants. Our data provide compelling genetic evidence that the end-capping activity of CP is inhibited by membrane signaling lipids in eukaryotic cells. Specifically, CP acts as a PA biosensor and key transducer of fluxes in membrane signaling phospholipids into changes in actin cytoskeleton dynamics

    The Hyperfine Splitting in Charmonium: Lattice Computations Using the Wilson and Clover Fermion Actions

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    We compute the hyperfine splitting mJ/ψmηcm_{J/\psi}-m_{\eta_c} on the lattice, using both the Wilson and O(a)O(a)-improved (clover) actions for quenched quarks. The computations are performed on a 243×4824^3\times48 lattice at β=6.2\beta = 6.2, using the same set of 18 gluon configurations for both fermion actions. We find that the splitting is 1.83\err{13}{15} times larger with the clover action than with the Wilson action, demonstrating the sensitivity of the spin-splitting to the magnetic moment term which is present in the clover action. However, even with the clover action the result is less than half of the physical mass-splitting. We also compute the decay constants fηcf_{\eta_c} and fJ/ψ1f^{-1}_{J/\psi}, both of which are considerably larger when computed using the clover action than with the Wilson action. For example for the ratio fJ/ψ1/fρ1f^{-1}_{J/\psi}/f^{-1}_{\rho} we find 0.32\err{1}{2} with the Wilson action and 0.48±30.48\pm 3 with the clover action (the physical value is 0.44(2)).Comment: LaTeX file, 8 pages and two postscript figures. Southampton Preprint: SHEP 91/92-27 Edinburgh Preprint: 92/51
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