4,633 research outputs found

    Radio-quiet and radio-loud pulsars: similar in Gamma-rays but different in X-rays

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    We present new Chandra and XMM-Newton observations of a sample of eight radio-quiet Gamma-ray pulsars detected by the Fermi Large Area Telescope. For all eight pulsars we identify the X-ray counterpart, based on the X-ray source localization and the best position obtained from Gamma-ray pulsar timing. For PSR J2030+4415 we found evidence for an about 10 arcsec-long pulsar wind nebula. Our new results consolidate the work from Marelli et al. 2011 and confirm that, on average, the Gamma-ray--to--X-ray flux ratios (Fgamma/Fx) of radio-quiet pulsars are higher than for the radio-loud ones. Furthermore, while the Fgamma/Fx distribution features a single peak for the radio-quiet pulsars, the distribution is more dispersed for the radio-loud ones, possibly showing two peaks. We discuss possible implications of these different distributions based on current models for pulsar X-ray emission.Comment: Accepted for publication in The Astrophysical Journal; 12 pages, 3 figures, 2 table

    Spin-Peierls transition in TiOCl

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    Temperature-dependent x-ray diffraction of the low-dimensional spin 1/2 quantum magnet TiOCl shows that the phase transition at T_{c2} = 90 K corresponds to a lowering of the lattice symmetry. Below T_{c1} = 66 K a twofold superstructure develops, that indicates the formation of spin-singlet pairs via direct exchange between neighboring Ti atoms, while the role of superexchange is found to be negligible. TiOCl thus is identified as a spin-Peierls system of pure 1D chains of atoms. The first-order character of the transition at T_{c1} is explained by the competition between the structurally deformed state below T_{c2} and the spin-Peierls state below T_{c1}.Comment: Phys. Rev. B (Rapid Communications) in pres

    Finite Size Scaling of the 2D Six-Clock model

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    We investigate the isotropic-anisotropic phase transition of the two-dimensional XY model with six-fold anisotropy, using Monte Carlo renormalization group method. The result indicates difficulty of observing asymptotic critical behavior in Monte Carlo simulations, owing to the marginal flow at the fixed point.Comment: Short note. revtex, 6 pages, 3 figures. To appear in J. Phys. Soc. Jpn. Vol.70 No. 2 (Feb 2001

    New Dependencies of Hierarchies in Polynomial Optimization

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    We compare four key hierarchies for solving Constrained Polynomial Optimization Problems (CPOP): Sum of Squares (SOS), Sum of Diagonally Dominant Polynomials (SDSOS), Sum of Nonnegative Circuits (SONC), and the Sherali Adams (SA) hierarchies. We prove a collection of dependencies among these hierarchies both for general CPOPs and for optimization problems on the Boolean hypercube. Key results include for the general case that the SONC and SOS hierarchy are polynomially incomparable, while SDSOS is contained in SONC. A direct consequence is the non-existence of a Putinar-like Positivstellensatz for SDSOS. On the Boolean hypercube, we show as a main result that Schm\"udgen-like versions of the hierarchies SDSOS*, SONC*, and SA* are polynomially equivalent. Moreover, we show that SA* is contained in any Schm\"udgen-like hierarchy that provides a O(n) degree bound.Comment: 26 pages, 4 figure

    Combination of improved multibondic method and the Wang-Landau method

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    We propose a method for Monte Carlo simulation of statistical physical models with discretized energy. The method is based on several ideas including the cluster algorithm, the multicanonical Monte Carlo method and its acceleration proposed recently by Wang and Landau. As in the multibondic ensemble method proposed by Janke and Kappler, the present algorithm performs a random walk in the space of the bond population to yield the state density as a function of the bond number. A test on the Ising model shows that the number of Monte Carlo sweeps required of the present method for obtaining the density of state with a given accuracy is proportional to the system size, whereas it is proportional to the system size squared for other conventional methods. In addition, the new method shows a better performance than the original Wang-Landau method in measurement of physical quantities.Comment: 12 pages, 3 figure

    Broad histogram relation for the bond number and its applications

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    We discuss Monte Carlo methods based on the cluster (graph) representation for spin models. We derive a rigorous broad histogram relation (BHR) for the bond number; a counterpart for the energy was derived by Oliveira previously. A Monte Carlo dynamics based on the number of potential moves for the bond number is proposed. We show the efficiency of the BHR for the bond number in calculating the density of states and other physical quantities.Comment: 7 pages, 7 figure

    Development and performance of the Clinical Trials ESSDAI (ClinTrialsESSDAI), consisting of frequently active clinical domains, in two randomised controlled trials in primary Sjogren's syndrome

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    Objective. To develop and evaluate the Clinical Trials EULAR Sjogren's Syndrome Disease Activity Index (ClinTrialsESSDAI), consisting of frequently active clinical domains of the ESSDAI, using two randomised controlled trials in primary Sjogren's syndrome (pSS). Methods. The ASAP-III trial in abatacept (80 pSS patients) and TRACTISS trial in rituximab (133 pSS patients) were analysed. The most frequently active clinical domains were selected, and ClinTrialsESSDAI total score was calculated using existing weightings of the ClinESSDAI (which also excludes the biological domain). Performance of the ClinTrialsESSDAI was compared to ClinESSDAI and ESSDAI. Responsiveness was assessed using standardised response mean (SRM), and discrimination was assessed using adjusted mean difference. Results. Besides the biological domain, the most frequently active domains were glandular, articular, haematological, constitutional, lymphadenopathy and cutaneous. These domains were selected for the ClinTrialsESSDAI. At primary endpoint visits, SRM values of ClinTrialsESSDAI, ClinESSDAI and ESSDAI were respectively -0.65/-0.59, -0.63/-0.59 and - 0.64/-0.61 for abatacept/placebo and -0.33/-0.13, -0.34/0.12 and -0.41/-0.16 for rituximab/placebo. Adjusted mean differences between active treatment and placebo groups were respectively -1.7, -1.4 and -1.1 for ASAP-III and -1.1, -1.1 and -1.2 for TRACTISS. Conclusion. The ClinTrialsESSDAI, consisting of six frequently active clinical domains of the ESSDAI, shows closely similar responsiveness and discrimination between treatment groups compared to the ClinESSDAI and ESSDAI. Therefore, this ClinTrialsESSDAI is not preferable to ClinESSDAI and ESSDAI for use as primary endpoint. A composite endpoint combining response at multiple clinically relevant items seems more suitable as primary study endpoint in pSS

    Insights in a restricted temporary pacemaker strategy in a lean transcatheter aortic valve implantation program

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    OBJECTIVES: To study the safety and feasibility of a restrictive temporary‐RV‐pacemaker use and to evaluate the need for temporary pacemaker insertion for failed left ventricular (LV) pacing ability (no ventricular capture) or occurrence of high‐degree AV‐blocks mandating continuous pacing. BACKGROUND: Ventricular pacing remains an essential part of contemporary transcatheter aortic valve implantation (TAVI). A temporary‐right‐ventricle (RV)‐pacemaker lead is the standard approach for transient pacing during TAVI but requires central venous access. METHODS: An observational registry including 672 patients who underwent TAVI between June 2018 and December 2020. Patients received pacing on the wire when necessary, unless there was a high‐anticipated risk for conduction disturbances post‐TAVI, based on the baseline‐ECG. The follow‐up period was 30 days. RESULTS: A temporary‐RV‐pacemaker lead (RVP‐cohort) was inserted in 45 patients, pacing on the wire (LVP‐cohort) in 488 patients, and no pacing (NoP‐cohort) in 139 patients. A bailout temporary pacemaker was implanted in 14 patients (10.1%) in the NoP‐cohort and in 24 patients (4.9%) in the LVP‐cohort. One patient in the LVP‐cohort needed an RV‐pacemaker for incomplete ventricular capture. Procedure time was significantly longer in the RVP‐cohort (68 min [IQR 52–88.] vs. 55 min [IQR 44–72] in NoP‐cohort and 55 min [IQR 43–71] in the LVP‐cohort [p < 0.005]). Procedural high‐degree AV‐block occurred most often in the RVP‐cohort (45% vs. 14% in the LVP and 16% in the NoP‐cohort [p ≤ 0.001]). Need for new PPI occurred in 47% in the RVP‐cohort, versus 20% in the NoP‐cohort and 11% in the LVP‐cohort (p ≤ 0.001). CONCLUSION: A restricted RV‐pacemaker strategy is safe and shortens procedure time. The majority of TAVI‐procedures do not require a temporary‐RV‐pacemaker
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