168,483 research outputs found

    Doppler Amplification of Motion of a Trapped Three-Level Ion

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    The system of a trapped ion translationally excited by a blue-detuned near-resonant laser, sometimes described as an instance of a phonon laser, has recently received attention as interesting in its own right and for its application to non-destructive readout of internal states of non-fluorescing ions. Previous theoretical work has been limited to cases of two-level ions. Here, we perform simulations to study the dynamics of a phonon laser involving the Λ\Lambda-type ^{138}\mbox{Ba}^{+} ion, in which coherent population trapping effects lead to different behavior than in the previously studied cases. We also explore optimization of the laser parameters to maximize amplification gain and signal-to-noise ratio for internal state readout

    Image Properties of Embedded Lenses

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    We give analytic expressions for image properties of objects seen around point mass lenses embedded in a flat Λ\LambdaCDM universe. An embedded lens in an otherwise homogeneous universe offers a more realistic representation of the lens's gravity field and its associated deflection properties than does the conventional linear superposition theory. Embedding reduces the range of the gravitational force acting on passing light beams thus altering all quantities such as deflection angles, amplifications, shears and Einstein ring sizes. Embedding also exhibits the explicit effect of the cosmological constant on these same lensing quantities. In this paper we present these new results and demonstrate how they can be used. The effects of embedding on image properties, although small i.e., usually less than a fraction of a percent, have a more pronounced effect on image distortions in weak lensing where the effects can be larger than 10%. Embedding also introduces a negative surface mass density for both weak and strong lensing, a quantity altogether absent in conventional Schwarzschild lensing. In strong lensing we find only one additional quantity, the potential part of the time delay, which differs from conventional lensing by as much as 4%, in agreement with our previous numerical estimates.Comment: 17 pages, 6 figure

    A Note on Pretzelosity TMD Parton Distribution

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    We show that the transverse-momentum-dependent parton distribution, called as Pretzelosity function, is zero at any order in perturbation theory of QCD for a single massless quark state. This implies that Pretzelosity function is not factorized with the collinear transversity parton distribution at twist-2, when the struck quark has a large transverse momentum. Pretzelosity function is in fact related to collinear parton distributions defined with twist-4 operators. In reality, Pretzelosity function of a hadron as a bound state of quarks and gluons is not zero. Through an explicit calculation of Pretzelosity function of a quark combined with a gluon nonzero result is found.Comment: improved explanation, published version in Phys. Lett.

    Multitarget Tracking in Nonoverlapping Cameras Using a Reference Set

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    Tracking multiple targets in nonoverlapping cameras are challenging since the observations of the same targets are often separated by time and space. There might be significant appearance change of a target across camera views caused by variations in illumination conditions, poses, and camera imaging characteristics. Consequently, the same target may appear very different in two cameras. Therefore, associating tracks in different camera views directly based on their appearance similarity is difficult and prone to error. In most previous methods, the appearance similarity is computed either using color histograms or based on pretrained brightness transfer function that maps color between cameras. In this paper, a novel reference set based appearance model is proposed to improve multitarget tracking in a network of nonoverlapping cameras. Contrary to previous work, a reference set is constructed for a pair of cameras, containing subjects appearing in both camera views. For track association, instead of directly comparing the appearance of two targets in different camera views, they are compared indirectly via the reference set. Besides global color histograms, texture and shape features are extracted at different locations of a target, and AdaBoost is used to learn the discriminative power of each feature. The effectiveness of the proposed method over the state of the art on two challenging real-world multicamera video data sets is demonstrated by thorough experiments

    Heterodimerization of apelin receptor and neurotensin receptor 1 induces phosphorylation of ERK1/2 and cell proliferation via Gαq-mediated mechanism

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    Dimerization of G protein-coupled receptors (GPCRs) is crucial for receptor function including agonist affinity, efficacy, trafficking and specificity of signal transduction, including G protein coupling. Emerging data suggest that the cardiovascular system is the main target of apelin, which exerts an overall neuroprotective role, and is a positive regulator of angiotensin-converting enzyme 2 (ACE2) in heart failure. Moreover, ACE2 cleaves off C-terminal residues of vasoactive peptides including apelin-13, and neurotensin that activate the apelin receptor (APJ) and neurotensin receptor 1 (NTSR1) respectively, that belong to the A class of GPCRs. Therefore, based on the similar mode of modification by ACE2 at peptide level, the homology at amino acid level and the capability of forming dimers with other GPCRs, we have been suggested that APJ and NTSR1 can form a functional heterodimer. Using co-immunoprecipitation, BRET and FRET, we provided conclusive evidence of heterodimerization between APJ and NTSR1 in a constitutive and induced form. Upon agonist stimulation, hetrodimerization enhanced ERK1/2 activation and increased proliferation via activation of Gq α-subunits. These novel data provide evidence for a physiological role of APJ/NTSR1 heterodimers in terms of ERK1/2 activation and increased intracellular calcium and induced cell proliferation and provide potential new pharmaceutical targets for cardiovascular disease. © 2014 The Authors
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