882 research outputs found

    Investigating the validity of IEEE 802.11 MAC modeling hypotheses

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    As WLANs employing IEEE 802.11 have become pervasive, many analytic models for predicting their performance have been developed in recent years. Due to the complicated nature of the 802.11 MAC operation, approximations must be made to enable tractable mathematical models. In this article, through simulation we investigate the veracity of the approximations shared by many models that have been developed starting with the fundamental hypotheses in Bianchipsilas (1998 and 2000) seminal papers. We find that even for small numbers of station these assumptions that hold true for saturated stations (those that always have a packet to send) and for unsaturated stations with small buffers. However, despite their widespread adoption, we find that the commonly adopted assumptions that are used to incorporate station buffers are not appropriate. This raises questions about the predictive power of models based on these hypotheses

    Electron correlation energy in confined two-electron systems

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    Radial, angular and total correlation energies are calculated for four two-electron systems with atomic numbers Z=0-3 confined within an impenetrable sphere of radius R. We report accurate results for the non-relativistic, restricted Hartree-Fock and radial limit energies over a range of confinement radii from 0.05 - 10 a0. At small R, the correlation energies approach limiting values that are independent of Z while at intermediate R, systems with Z > 1 exhibit a characteristic maximum in the correlation energy resulting from an increase in the angular correlation energy which is offset by a decrease in the radial correlation energy

    Polarized Dirac fermions in de Sitter spacetime

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    The tetrad gauge invariant theory of the free Dirac field in two special moving charts of the de Sitter spacetime is investigated pointing out the operators that commute with the Dirac one. These are the generators of the symmetry transformations corresponding to isometries that give rise to conserved quantities according to the Noether theorem. With their help the plane wave spinor solutions of the Dirac equation with given momentum and helicity are derived and the final form of the quantum Dirac field is established. It is shown that the canonical quantization leads to a correct physical interpretation of the massive or massless fermion quantum fields.Comment: 19 pages, LaTeX w AMS sym

    Nonlinear spinor field in Bianchi type-I Universe filled with viscous fluid: numerical solutions

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    We consider a system of nonlinear spinor and a Bianchi type I gravitational fields in presence of viscous fluid. The nonlinear term in the spinor field Lagrangian is chosen to be λF\lambda F, with λ\lambda being a self-coupling constant and FF being a function of the invariants II an JJ constructed from bilinear spinor forms SS and PP. Self-consistent solutions to the spinor and BI gravitational field equations are obtained in terms of τ\tau, where τ\tau is the volume scale of BI universe. System of equations for τ\tau and \ve, where \ve is the energy of the viscous fluid, is deduced. This system is solved numerically for some special cases.Comment: 15 pages, 4 figure

    Striped antiferromagnetic order and electronic properties of stoichiometric LiFeAs from first-principles calculations

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    We investigate the structural, electronic, and magnetic properties of stoichiometric LiFeAs by using state-of-the-arts first-principles method. We find the magnetic ground-state by comparing the total energies among all the possible magnetic orders. Our calculated internal positions of Li and As are in good agreement with experiment. Our results show that stoichiometric LiFeAs has almost the same striped antiferromagnetic spin order as other FeAs-based parent compounds and tetragonal FeSe do, and the experimental fact that no magnetic phase transition has been observed at finite temperature is attributed to the tiny inter-layer spin coupling

    The Isgur-Wise function in a relativistic model for qQˉq\bar Q system

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    We use the Dirac equation with a ``(asymptotically free) Coulomb + (Lorentz scalar) linear '' potential to estimate the light quark wavefunction for qQˉ q\bar Q mesons in the limit mQ→∞m_Q\to \infty. We use these wavefunctions to calculate the Isgur-Wise function ξ(v.v′)\xi (v.v^\prime ) for orbital and radial ground states in the phenomenologically interesting range 1≤v.v′≤41\leq v.v^ \prime \leq 4. We find a simple expression for the zero-recoil slope, ξ′(1)=−1/2−ϵ2/3\xi^ \prime (1) =-1/2- \epsilon^2 /3, where ϵ\epsilon is the energy eigenvalue of the light quark, which can be identified with the Λˉ\bar\Lambda parameter of the Heavy Quark Effective Theory. This result implies an upper bound of −1/2-1/2 for the slope ξ′(1)\xi^\prime (1). Also, because for a very light quark q(q=u,d)q (q=u, d) the size \sqrt {} of the meson is determined mainly by the ``confining'' term in the potential (γ∘σr)(\gamma_\circ \sigma r), the shape of ξu,d(v.v′)\xi_{u,d}(v.v^\prime ) is seen to be mostly sensitive to the dimensionless ratio Λˉu,d2/σ\bar \Lambda_{u,d}^2/\sigma. We present results for the ranges of parameters 150MeV<Λˉu,d<600MeV150 MeV <\bar \Lambda_{u,d} <600 MeV (Λˉs≈Λˉu,d+100MeV)(\bar\Lambda_s \approx \bar\Lambda_{u,d}+100 MeV), 0.14GeV2≤σ≤0.25GeV20.14 {GeV}^2 \leq \sigma \leq 0.25 {GeV}^2 and light quark masses mu,md≈0,ms=175MeVm_u, m_d \approx 0, m_s=175 MeV and compare to existing experimental data and other theoretical estimates. Fits to the data give: Λˉu,d2/σ=4.8±1.7{\bar\Lambda_{u,d}}^2/\sigma =4.8\pm 1.7 , −ξu,d′(1)=2.4±0.7-\xi^\prime_{u,d}(1)=2.4\pm 0.7 and ∣Vcb∣τB1.48ps=0.050±0.008\vert V_{cb} \vert \sqrt {\frac {\tau_B}{1.48 ps}}=0.050\pm 0.008 [ARGUS '93]; Λˉu,d2/σ=3.4±1.8{\bar\Lambda_{u,d}}^2/\sigma = 3.4\pm 1.8, −ξu,d′(1)=1.8±0.7-\xi^\prime_{u,d}(1)=1.8\pm 0.7 and ∣Vcb∣τB1.48ps=0.043±0.008\vert V_{cb} \vert \sqrt { \frac {\tau_B}{1.48 ps}}=0.043\pm 0.008 [CLEO '93]; ${\bar\Lambda_{u,d}}^2/Comment: 22 pages, Latex, 4 figures (not included) available by fax or via email upon reques

    An inhaled bioadhesive hydrogel to shield non-human primates from SARS-CoV-2 infection

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    The surge of fast-spreading SARS-CoV-2 mutated variants highlights the need for fast, broad-spectrum strategies to counteract viral infections. In this work, we report a physical barrier against SARS-CoV-2 infection based on an inhalable bioadhesive hydrogel, named spherical hydrogel inhalation for enhanced lung defence (SHIELD). Conveniently delivered via a dry powder inhaler, SHIELD particles form a dense hydrogel network that coats the airway, enhancing the diffusional barrier properties and restricting virus penetration. SHIELD’s protective effect is first demonstrated in mice against two SARS-CoV-2 pseudo-viruses with different mutated spike proteins. Strikingly, in African green monkeys, a single SHIELD inhalation provides protection for up to 8 hours, efficiently reducing infection by the SARS-CoV-2 WA1 and B.1.617.2 (Delta) variants. Notably, SHIELD is made with food-grade materials and does not affect normal respiratory functions. This approach could offer additional protection to the population against SARS-CoV-2 and other respiratory pathogens

    Hepatitis C virus nonstructural protein 5A (NS5A) is an RNA-binding protein

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    Hepatitis C virus (HCV) nonstructural protein 5A (NS5A) has been shown to antagonize numerous cellular pathways, including the antiviral interferon-α response. However, the capacity of this protein to interact with the viral polymerase suggests a more direct role for NS5A in genome replication. In this study, we employed two bacterially expressed, soluble derivatives of NS5A to probe for novel functions of this protein. We find that NS5A has the capacity to bind ! to the 3′-ends of HCV plus and minus strand RNAs. The high affinity binding site for NS5A in the 3′-end of plus strand RNA maps to the polypyrimidine tract, an element known to be essential for genome replication and infectivity. NS5A has a preference for single-stranded RNA containing stretches of uridine or guanosine. Values for the equilibrium dissociation constants for high affinity binding sites were in the 10 nM range. Two-dimensional gel electrophoresis followed by Western blotting revealed the presence of unphosphorylated NS5A in Huh-7 cells stably expressing the subgenomic replicon. Moreover, RNA immunoprecipitation and NS5A pull-down experiments showed the capacity of replicon-derived NS5A to bind to synthetic RNA and the HCV genome, respectively. Deletion of all of the casein kinase II phosphorylation sites in NS5A supported stable replication of a subgenomic replicon in Huh-7. However, this derivative could not be labeled with inorganic phosphate, suggesting that extensive phosphorylation of NS5A is not required for the replication functions of NS5A. The discovery that NS5A is an RNA-binding protein defines a new functional target for development of agents to treat HCV infection and a new structural class of RNA-binding proteins. © 2005 by The American Society for Biochemistry and Molecular Biology, Inc

    Nonequilibrium Josephson effect in short-arm diffusive SNS interferometers

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    We study non-equilibrium Josephson effect and phase-dependent conductance in three-terminal diffusive interferometers with short arms. We consider strong proximity effect and investigate an interplay of dissipative and Josephson currents co-existing within the same proximity region. In junctions with transparent interfaces, the suppression of the Josephson current appears at rather large voltage, eV∼ΔeV\sim \Delta, and the current vanishes at eV≥ΔeV\geq\Delta. Josephson current inversion becomes possible in junctions with resistive interfaces, where the inversion occurs within a finite interval of the applied voltage. Due to the presence of considerably large and phase-dependent injection current, the critical current measured in a current biased junction does not coincide with the maximum Josephson current, and remains finite when the true Josephson current is suppressed. The voltage dependence of the conductance shows two pronounced peaks, at the bulk gap energy, and at the proximity gap energy; the phase oscillation of the conductance exhibits qualitatively different form at small voltage eV<ΔeV<\Delta, and at large voltage eV>ΔeV>\Delta.Comment: 11 pages, 9 figures, revised version, to be published in Phys. Rev.

    Mast cell deficiency limits the development of chronic rhinosinusitis in mice

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    Background: Chronic rhinosinusitis (CRS) is one of the most common chronic diseases in adults in both developing and developed countries. The etiology and pathogenesis of CRS remain poorly understood, and the disease is refractory to therapy in many patients. Mast cell activation has been demonstrated in the sinonasal mucosa of patients with CRS; however, the specific contribution of mast cells to the development and pathogenesis of this disease has not been established. Objective: The objective of this study was to investigate the role of mast cells in the development of CRS. Methods: C57BL/6 wild-type and C57BL/6-KitW-sh/W-sh mast cell-deficient mice were immunized by intraperitoneal allergen injection and subsequent chronic low dose intranasal allergen challenges. The sinonasal phenotypes of these groups were then evaluated and compared to saline-treated controls using radiologic, histologic, and immunologic methods. Results: Wild-type mice exposed to chronic intranasal allergen developed many features seen in human CRS, including mucosal thickening, cystic changes, polyp development, eosinophilia, goblet cell hyperplasia, and mast cell activation. In contrast, sinonasal pathology was significantly attenuated in mast cell-deficient mice subjected to the same chronic allergen protocol. Specifically, tissue eosinophilia and goblet cell hyperplasia were reduced by approximately 50% compared to wild-type levels. Surprisingly, none of the mast cell-deficient mice subjected to chronic allergen challenge developed cystic changes or polypoid changes in the nose or sinuses. Conclusions: These data identify a critical role for mast cells in the development of many features of a mouse model of eosinophilic CRS, suggesting that therapeutic strategies targeting mast cells be examined in humans afflicted with this disease
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