10,943 research outputs found

    Convergence of the Lasserre Hierarchy of SDP Relaxations for Convex Polynomial Programs without Compactness

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    The Lasserre hierarchy of semidefinite programming (SDP) relaxations is an effective scheme for finding computationally feasible SDP approximations of polynomial optimization over compact semi-algebraic sets. In this paper, we show that, for convex polynomial optimization, the Lasserre hierarchy with a slightly extended quadratic module always converges asymptotically even in the face of non-compact semi-algebraic feasible sets. We do this by exploiting a coercivity property of convex polynomials that are bounded below. We further establish that the positive definiteness of the Hessian of the associated Lagrangian at a saddle-point (rather than the objective function at each minimizer) guarantees finite convergence of the hierarchy. We obtain finite convergence by first establishing a new sum-of-squares polynomial representation of convex polynomials over convex semi-algebraic sets under a saddle-point condition. We finally prove that the existence of a saddle-point of the Lagrangian for a convex polynomial program is also necessary for the hierarchy to have finite convergence.Comment: 17 page

    Chiral Anomaly Effects and the BaBar Measurements of the γγπ0\gamma\gamma^{*}\to \pi^{0} Transition Form Factor

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    The recent BaBar measurements of the γγπ0\gamma\gamma^{*}\to \pi^{0} transition form factor show spectacular deviation from perturbative QCD prediction for large space-like Q2Q^{2} up to 34GeV234\,\rm GeV^{2}. When plotted against Q2Q^{2}, Q2F(Q2)Q^{2}F(Q^{2}) shows steady increase with Q2Q^{2} in contrast with the flat Q2Q^{2} behavior predicted by perturbative QCD, and at 34GeV234\,\rm GeV^{2} is more than 50% larger than the QCD prediction. Stimulated by the BaBar measurements, we revisit our previous paper on the cancellation of anomaly effects in high energy processes Z0π0γZ^{0}\to \pi^{0}\gamma, e+eπ0γe^{+}e^{-}\to \pi^{0}\gamma and apply our results to the γγπ0\gamma^{*}\gamma\to \pi^{0} transition form factor measured in the e+ee+eπ0e^{+}e^{-}\to e^{+}e^{-}\pi^{0} process with one highly virtual photon. We find that, the transition form factor F(Q2)F(Q^{2}) behaves as (m2Q2)×(ln(Q2/m2))2(\frac{m^{2}}{Q^{2}})\times (\ln(Q^{2}/m^{2}))^{2} and produces a striking agreement with the BaBar data for Q2F(Q2)Q^{2}F(Q^{2}) with m=132MeVm=132\,\rm MeV which also reproduces very well the CLEO data at lower Q2Q^{2}.Comment: v4, LaTeX, 8 pages, one figure, minor changes(references), to appear in Int. J. Mod. Phys.

    Charmless Final State Interaction in B-> pi pi decays

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    We estimate effects of the final state interactions in B -> pi pi decays coming from rescattering of pi pi via exchange of rho, sigma, f_0 mesons. Then we include the rho rho rescattering via exchange of pi, omega, a_1 mesons and finally we consider contributions of the a_1 pi rescattering via exchange of rho. The absorptive parts of amplitudes for these processes are determined. In the case of pi^+ pi^- decay mode, due to model uncertainties, the calculated contribution is |M_A| =< 1.7 x 10^-8 GeV. This produces a small relative strong phase for the tree and color-suppressed B -> pi pi amplitudes consistent with the result of a recent phenomenological analysis based on the BaBar and Belle results for the B -> pi pi branching ratios and CP asymmetries.Comment: 10 pages, 2 figure

    Urine adulteration: Can bleach be used to mask MDMA use?

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    Concerns regarding specimen integrity have long been a major issue of urine drug testing due to acts of urine adulteration. At a high concentration, in vitro urine adulteration using sodium hypochlorite (bleach) produced false-negative results for 3,4-methylenedioxymethamphetamine (MDMA) in CEDIA® immunoassay screening with strong negative readings. However, these strong negative readings may act as a warning sign for further investigation of the sample where the detection of a unique marker in the form of N-chloroMDMA will suggest urine adulteration via bleach. Liquid chromatography-tandem mass spectrometry (LC-MS/MS) identified N-chloroMDMA is a major product formed between hypochlorite and MDMA in urine. N-ChloroMDMA was found stable at 4°C for at least 10 h, but decomposed over time at room temperature (20°C) with MDMA being identified as one of its main decomposition products. © 2013 The Royal Society of Chemistry

    The Distribution of Dengue Virus Serotype in Quang Nam Province (Vietnam) during the Outbreak in 2018

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    Objectives: Quang Nam province in the Centre of Vietnam has faced an outbreak of dengue hemorrhagic fever (DHF) in 2018. Although DHF is a recurrent disease in this area, no epidemiological and microbiological reports on dengue virus serotypes have been conducted mainly due to lack of facilities for such a kind of advanced surveillance. The aim of this study was to detect different dengue virus serotypes in patients’ blood samples. Design and Methods: Suspected cases living in Quang Nam province (Vietnam) and presenting clinical and hematological signs of dengue hemorrhagic fever were included in the study. The screening was performed, and the results were compared by using two methodologies: RT real-time PCR (RT-rPCR) and the Dengue NS1 rapid test. Results: From December 2018 to February 2019, looking both at RT-rPCR [+] and NS1 [+] methodologies, a total of 488 patients were screened and 336 were positive for dengue virus detection (74 children and 262 adults); 273 of these patients (81.3%) underwent viral serotype identification as follows: 12.82% (35/273) D1 serotype, 17.95% (49/273) D2, 0.37% (1/273) D3, 68.50 (187/283) D4, and 0.37% (1/273) D2+D4 serotypes. The RT-rPCR outcomes showed higher sensitivity during the first three days of infection compared to NS1 (92.3% vs. 89.7%). The NS1 increased sensitivity after the first 3 days whilst the RT-rPCR decreased. Conclusions: Advanced surveillance with dengue virus serotypes identification, if performed routinely, may help to predict and prevent further DHF epidemics based on the exposure of the different serotypes during different periods that lead to the intensification of disease severity as a consequence of antibody-dependent enhancement (ADE)
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