402,454 research outputs found

    A characterization of the Razak-Jacelon algebra

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    Combing Elliott, Gong, Lin and Niu's result and Castillejos and Evington's result, we see that if AA is a simple separable nuclear monotracial C∗^*-algebra, then A⊗WA\otimes\mathcal{W} is isomorphic to W\mathcal{W} where W\mathcal{W} is the Razak-Jacelon algebra. In this paper, we give another proof of this. In particular, we show that if D\mathcal{D} is a simple separable nuclear monotracial M2∞M_{2^{\infty}}-stable C∗^*-algebra which is KKKK-equivalent to {0}\{0\}, then D\mathcal{D} is isomorphic to W\mathcal{W} without considering tracial approximations of C∗^*-algebras with finite nuclear dimension. Our proof is based on Matui and Sato's technique, Schafhauser's idea in his proof of the Tikuisis-White-Winter theorem and properties of Kirchberg's central sequence C∗^*-algebra F(D)F(\mathcal{D}) of D\mathcal{D}. Note that some results for F(D)F(\mathcal{D}) is based on Elliott-Gong-Lin-Niu's stable uniqueness theorem. Also, we characterize W\mathcal{W} by using properties of F(W)F(\mathcal{W}). Indeed, we show that a simple separable nuclear monotracial C∗^*-algebra DD is isomorphic to W\mathcal{W} if and only if DD satisfies the following properties:(i) for any θ∈[0,1]\theta\in [0,1], there exists a projection pp in F(D)F(D) such that τD,ω(p)=θ\tau_{D, \omega}(p)=\theta,(ii) if pp and qq are projections in F(D)F(D) such that 0<τD,ω(p)=τD,ω(q)0<\tau_{D, \omega}(p)=\tau_{D, \omega}(q), then pp is Murray-von Neumann equivalent to qq,(iii) there exists a homomorphism from DD to W\mathcal{W}.Comment: added references, fixed typos, 23 page

    A New HDG Method for Dirichlet Boundary Control of Convection Diffusion PDEs II: Low Regularity

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    In the first part of this work, we analyzed a Dirichlet boundary control problem for an elliptic convection diffusion PDE and proposed a new hybridizable discontinuous Galerkin (HDG) method to approximate the solution. For the case of a 2D polygonal domain, we also proved an optimal superlinear convergence rate for the control under certain assumptions on the domain and on the target state. In this work, we revisit the convergence analysis without these assumptions; in this case, the solution can have low regularity and we use a different analysis approach. We again prove an optimal convergence rate for the control, and present numerical results to illustrate the convergence theory

    A Simple Demonstration of the Doppler Effect in Sound

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    The example which is perhaps most frequently cited as an illustration of the Doppler effect is the change of pitch of a locomotive bell or whistle or of a street-car gong in rapid motion, particularly as heard by a person on board a car passing rapidly in the opposite direction on a parallel track. To the use of this illustration Professor R. W. Wood objects on the ground that scarcely one person in ten has any distinct recollection of having noticed the phenomena unless his attention has been directed to it

    Quantifying and Transferring Contextual Information in Object Detection

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    (c) 2012 IEEE. Personal use of this material is permitted. Permission from IEEE must be obtained for all other users, including reprinting/ republishing this material for advertising or promotional purposes, creating new collective works for resale or redistribution to servers or lists, or reuse of any copyrighted components of this work in other work

    Complete genome sequence of a sub-subgenotype 2.1i isolate of classical swine fever virus from China

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    Citation: Zhang, B., Mi, S., Bao, F., Guo, H., Tu, C., Shi, J., & Gong, W. (2017). Complete genome sequence of a sub-subgenotype 2.1i isolate of classical swine fever virus from China. Genome Announcements, 5(14). doi:10.1128/genomeA.00127-17The complete genome sequence of a sub-subgenotype 2.1i isolate of classical swine fever virus (CSFV), GD317/2011, was determined. Notably, GD317/2011 is distant from the sub-subgenotype 2.1b isolate HEBZ at genes of Erns, E1, E2, P7, NS2, NS5A and the 3=-nontranslated region (3=-NTR) but is closely related to that at genes of Npro, Core, NS3, NS4A, NS4B, and NS5B. © 2017 Zhang et al
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