3,259 research outputs found

    Inconsistency of QED in the Presence of Dirac Monopoles

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    A precise formulation of U(1)U(1) local gauge invariance in QED is presented, which clearly shows that the gauge coupling associated with the unphysical longitudinal photon field is non-observable and actually has an arbitrary value. We then re-examine the Dirac quantization condition and find that its derivation involves solely the unphysical longitudinal coupling. Hence an inconsistency inevitably arises in the presence of Dirac monopoles and this can be considered as a theoretical evidence against their existence. An alternative, independent proof of this conclusion is also presented.Comment: Extended and combined version, refinements added; 20 LaTex pages, Published in Z. Phys. C65, pp.175-18

    Holographic Gauge Theory with Maxwell Magnetic Field

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    We first apply the transformation of mixing azimuthal with wrapped coordinate to the 11D M-theory with a stack N M5-branes to find the spacetime of a stack of N D4-branes with magnetic field in 10D IIA string theory, after the Kaluza-Klein reduction. In the near-horizon limit the background becomes the Melvin magnetic field deformed AdS6×S4AdS_6 \times S^4. Although the solution represents the D-branes under the Melvin RR one-form we use a simple observation to see that it also describes the solution of D-branes under the Maxwell magnetic field. As the magnetic field we consider is the part of the background itself we have presented an alternative to previous literature, because our method does not require the assumption of negligible back reaction. Next, we use the found solution to investigate the meson property through D4/D8 system (Sakai-Sugimoto model) and compare it with those studied by other authors. Finally, we present a detailed analysis about the Wilson loop therein and results show that the external Maxwell magnetic field will enhance the quark-antiquark potential.Comment: Latex 14 pp, add fi

    Long-lived neutral-kaon flux measurement for the KOTO experiment

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    The KOTO (K0K^0 at Tokai) experiment aims to observe the CP-violating rare decay KLπ0ννˉK_L \rightarrow \pi^0 \nu \bar{\nu} by using a long-lived neutral-kaon beam produced by the 30 GeV proton beam at the Japan Proton Accelerator Research Complex. The KLK_L flux is an essential parameter for the measurement of the branching fraction. Three KLK_L neutral decay modes, KL3π0K_L \rightarrow 3\pi^0, KL2π0K_L \rightarrow 2\pi^0, and KL2γK_L \rightarrow 2\gamma were used to measure the KLK_L flux in the beam line in the 2013 KOTO engineering run. A Monte Carlo simulation was used to estimate the detector acceptance for these decays. Agreement was found between the simulation model and the experimental data, and the remaining systematic uncertainty was estimated at the 1.4\% level. The KLK_L flux was measured as (4.183±0.017stat.±0.059sys.)×107(4.183 \pm 0.017_{\mathrm{stat.}} \pm 0.059_{\mathrm{sys.}}) \times 10^7 KLK_L per 2×10142\times 10^{14} protons on a 66-mm-long Au target.Comment: 27 pages, 16 figures. To be appeared in Progress of Theoretical and Experimental Physic

    Measurement of the Phase Difference Between eta00 and eta+- to a Precision of 1^0

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    We propose to add an additional regenerator to the E731 spectrometer in the MC beamline to enable us to measure the phase difference between the CP violation parameters {eta}{sub 00} and {eta}{sub +-} to an accuracy of 1{sup o}. Very general considerations indicate that CPT conservation requires the phase difference, {Delta}{phi} = Arg({eta}{sub 00}) - Arg({eta}{sub +-}), to be smaller than one degree. The current experimental value is {Delta}{phi} = (9.4 {+-} 5.1){sup o}

    Measurement of Cosmic-ray Muons and Muon-induced Neutrons in the Aberdeen Tunnel Underground Laboratory

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    We have measured the muon flux and production rate of muon-induced neutrons at a depth of 611 m water equivalent. Our apparatus comprises three layers of crossed plastic scintillator hodoscopes for tracking the incident cosmic-ray muons and 760 L of gadolinium-doped liquid scintillator for producing and detecting neutrons. The vertical muon intensity was measured to be Iμ=(5.7±0.6)×106I_{\mu} = (5.7 \pm 0.6) \times 10^{-6} cm2^{-2}s1^{-1}sr1^{-1}. The yield of muon-induced neutrons in the liquid scintillator was determined to be Yn=(1.19±0.08(stat)±0.21(syst))×104Y_{n} = (1.19 \pm 0.08 (stat) \pm 0.21 (syst)) \times 10^{-4} neutrons/(μ\mu\cdotg\cdotcm2^{-2}). A fit to the recently measured neutron yields at different depths gave a mean muon energy dependence of Eμ0.76±0.03\left\langle E_{\mu} \right\rangle^{0.76 \pm 0.03} for liquid-scintillator targets.Comment: 14 pages, 17 figures, 3 table

    Search for the decay KL03γK_L^0 \rightarrow 3\gamma

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    We performed a search for the decay KL03γK_L^0 \rightarrow 3\gamma with the E391a detector at KEK. In the data accumulated in 2005, no event was observed in the signal region. Based on the assumption of KL03γK_L^0 \rightarrow 3\gamma proceeding via parity-violation, we obtained the single event sensitivity to be (3.23±0.14)×108(3.23\pm0.14)\times10^{-8}, and set an upper limit on the branching ratio to be 7.4×1087.4\times10^{-8} at the 90% confidence level. This is a factor of 3.2 improvement compared to the previous results. The results of KL03γK_L^0 \rightarrow 3\gamma proceeding via parity-conservation were also presented in this paper

    Acetylome of acinetobacter baumannii SK17 reveals a highly-conserved modification of histone-like protein HU

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    Lysine acetylation is a prevalent post-translational modification in both eukaryotes and prokaryotes. Whereas this modification is known to play pivotal roles in eukaryotes, the function and extent of this modification in prokaryotic cells remain largely unexplored. Here we report the acetylome of a pair of antibiotic-sensitive and -resistant nosocomial pathogen Acinetobacter baumannii SK17-S and SK17-R. A total of 145 lysine acetylation sites on 125 proteins was identified, and there are 23 acetylated proteins found in both strains, including histone-like protein HU which was found to be acetylated at Lys13. HU is a dimeric DNA-binding protein critical for maintaining chromosomal architecture and other DNA-dependent functions. To analyze the effects of site-specific acetylation, homogenously Lys13-acetylated HU protein, HU(K13ac) was prepared by genetic code expansion. Whilst not exerting an obvious effect on the oligomeric state, Lys13 acetylation alters both the thermal stability and DNA binding kinetics of HU. Accordingly, this modification likely destabilizes the chromosome structure and regulates bacterial gene transcription. This work indicates that acetyllysine plays an important role in bacterial epigenetics
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