19,738 research outputs found

    Stabilizing the electroweak vacuum by higher dimensional operators in a Higgs-Yukawa model

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    The Higgs boson discovery at the LHC with a mass of approximately 126 GeV suggests, that the electroweak vacuum of the standard model may be metastable at very high energies. However, any new physics beyond the standard model can change this picture. We want to address this important question within a lattice Higgs-Yukawa model as the limit of the standard model (SM). In this framework we will probe the effect of a higher dimensional operator for which we take a (ϕϕ)3(\phi^{\dagger}\phi)^3-term. Such a term could easily originate as a remnant of physics beyond the SM at very large scales. As a first step we investigate the phase diagram of the model including such a (ϕϕ)3(\phi^{\dagger}\phi)^3 operator. Exploratory results suggest the existence of regions in parameter space where first order transitions turn to second order ones, indicating the existence of a tri-critical line. We will explore the phase structure and the consequences for the stability of the SM, both analytically by investigating the constraint effective potential in lattice perturbation theory, and by studying the system non-perturbatively using lattice simulations.Comment: 7 pages, 6 figures; Proceedings of the 31st International Symposium on Lattice Field Theory - LATTICE 201

    Manifestations of Drag Reduction by Polymer Additives in Decaying, Homogeneous, Isotropic Turbulence

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    The existence of drag reduction by polymer additives, well established for wall-bounded turbulent flows, is controversial in homogeneous, isotropic turbulence. To settle this controversy we carry out a high-resolution direct numerical simulation (DNS) of decaying, homogeneous, isotropic turbulence with polymer additives. Our study reveals clear manifestations of drag-reduction-type phenomena: On the addition of polymers to the turbulent fluid we obtain a reduction in the energy dissipation rate, a significant modification of the fluid energy spectrum especially in the deep-dissipation range, a suppression of small-scale intermittency, and a decrease in small-scale vorticity filaments.Comment: 4 pages, 3 figure

    Arbitrarily large families of spaces of the same volume

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    In any connected non-compact semi-simple Lie group without factors locally isomorphic to SL_2(R), there can be only finitely many lattices (up to isomorphism) of a given covolume. We show that there exist arbitrarily large families of pairwise non-isomorphic arithmetic lattices of the same covolume. We construct these lattices with the help of Bruhat-Tits theory, using Prasad's volume formula to control their covolumes.Comment: 9 pages. Syntax corrected; one reference adde

    Visualisation of an entangled channel spin-1 system

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    Co-variance matrix formalism gives powerful entanglement criteria for continuous as well as finite dimensional systems. We use this formalism to study a mixed channel spin-1 system which is well known in nuclear reactions. A spin-j state can be visualized as being made up of 2j spinors which are represented by a constellation of 2j points on a Bloch sphere using Majorana construction. We extend this formalism to visualize an entangled mixed spin-1 system.Comment: 4 pages,4 figure

    Magnetotransport in the low carrier density ferromagnet EuB_6

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    We present a magnetotransport study of the low--carrier density ferromagnet EuB_6. This semimetallic compound, which undergoes two ferromagnetic transitions at T_l = 15.3 K and T_c = 12.5 K, exhibits close to T_l a colossal magnetoresistivity (CMR). We quantitatively compare our data to recent theoretical work, which however fails to explain our observations. We attribute this disagreement with theory to the unique type of magnetic polaron formation in EuB_6.Comment: Conference contribution MMM'99, San Jos

    Array CGH analysis and developmental delay: A diagnostic tool for neurologists

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    Developmental delay occurs in 1-3% of the population, with unknown etiology in approximately 50% of cases. Initial genetic work up for developmental delay previously included chromosome analysis and subtelomeric FISH (fluorescent in situ hybridization). Array Comparative Genomic Hybridization (aCGH) has emerged as a tool to detect genetic copy number changes and uniparental disomy and is the most sensitive test in providing etiological diagnosis in developmental delay. aCGH allows for the provision of prognosis and recurrence risks, improves access to resources, helps limit further investigations and may alter medical management in many cases. aCGH has led to the delineation of novel genetic syndromes associated with developmental delay. An illustrative case of a 31-year-old man with long standing global developmental delay and recently diagnosed 4q21 deletion syndrome with a deletion of 20.8 Mb genomic interval is provided. aCGH is now recommended as a first line test in children and adults with undiagnosed developmental delay and congenital anomalies

    Environmental effects of SPS: The middle atmosphere

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    The heavy lift launch vehicle associated with the solar power satellite (SPS) would deposit in the upper atmosphere exhaust and reentry products which could modify the composition of the stratosphere, mesosphere, and lower ionosphere. In order to assess such effects, atmospheric model simulations were performed, especially considering a geographic zone centered at the launch and reentry latitudes

    A Monopole-Antimonopole Solution of the SU(2) Yang-Mills-Higgs Model

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    As shown by Taubes, in the Bogomol'nyi-Prasad-Sommerfield limit the SU(2) Yang-Mills-Higgs model possesses smooth finite energy solutions, which do not satisfy the first order Bogomol'nyi equations. We construct numerically such a non-Bogomol'nyi solution, corresponding to a monopole-antimonopole pair, and extend the construction to finite Higgs potential.Comment: 11 pages, including 4 eps figures, LaTex format using RevTe

    MELAS: A multigenerational impact of the MTTL1 A3243G MELAS mutation

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    Background: the maternally inherited MTTL1 A3243G mutation in the mitochondrial genome causes MelaS (Mitochondrial encephalopathy lactic acidosis with Stroke-like episodes), a condition that is multisystemic but affects primarily the nervous system. Significant intra-familial variation in phenotype and severity of disease is well recognized. Methods: retrospective and ongoing study of an extended family carrying the MTTL1 A3243G mutation with multiple symptomatic individuals. tissue heteroplasmy is reviewed based on the clinical presentations, imaging studies, laboratory findings in affected individuals and pathological material obtained at autopsy in two of the family members. Results: there were seven affected individuals out of thirteen members in this three generation family who each carried the MTTL1 A3243G mutation. the clinical presentations were varied with symptoms ranging from hearing loss, migraines, dementia, seizures, diabetes, visual manifestations, and stroke like episodes. three of the family members are deceased from MelaS or to complications related to MelaS. Conclusions: the results of the clinical, pathological and radiological findings in this family provide strong support to the current concepts of maternal inheritance, tissue heteroplasmy and molecular pathogenesis in MelaS. neurologists (both adult and paediatric) are the most likely to encounter patients with MelaS in their practice. genetic counselling is complex in view of maternal inheritance and heteroplasmy. newer therapeutic options such as arginine are being used for acute and preventative management of stroke like episodes. © 2014 Canadian Journal of neurologiCal sciences inc
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