1,641 research outputs found

    Hidden-Sector Higgs Bosons at High-Energy Electron-Positron Colliders

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    The possibility of a scalar messenger that can couple the Standard Model (SM) to a hidden sector has been discussed in a variety of contexts in the literature in recent years. We consider the case that a new scalar singlet charged under an exotic spontaneously broken Abelian gauge symmetry mixes weakly with the SM Higgs resulting in two scalar mass states, one of which has heavily suppressed couplings to the SM particles. Previous phenomenological studies have focussed on potential signatures for such a model at the Large Hadron Collider (LHC). However, there are interesting regions of the parameter space in which the heavier Higgs state would be out of reach for LHC searches if its mass is greater than 1 TeV. We therefore investigate the discovery potential for such a particle at a 3 TeV electron-positron collider, which is motivated by the recent developments of the Compact Linear Collider (CLIC). We find that such an experiment could substantially extend our discovery reach for a heavy, weakly coupled Higgs boson, and we discuss three possible search channels.Comment: 14 pages, 8 Figures. Published as an LCD Not

    The Tango Tokio

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    [Verse 1] Way out West, all over the golden gate, They’ve a tango, gee, but it’s simply great! Oh! oh! oh! oh! it’s the nicest tune, I know, It is called the Japanese glide away; You should see those Japanese slide away, When they play it, ev’rybody starts to sway it: [Chorus] Oh, oh, you Jap, little Jap, little Jap, little Japanese! Oh, oh, you cute little yap, little yap, little yapanese! How we live to see you prance, When they play that tango dance; It just puts us in a trance Oh, pinky panky poo, pinky panky poo! Oh, oh, you sly little, sly little, sly little Japaneses! You are a fly little, fly little, fly little Japanese! Tho’ you sometimes make us mad, If you want to make us glad, Do that teasing Tango Tokio. [Verse 2] When you hear that Tokio Tango tune, You’ll go dip, dip, dippy and pretty soon You’ll start swaying, just like this and just like that; You’ll imagine you are in Tokio, You will go clean clean off your kokio, If you know it, all day long you’d want to do it: [Chorus

    Why Take Both Boxes?

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    The crucial premise of the standard argument for two‐boxing in Newcomb's problem, a causal dominance principle, is false. We present some counterexamples. We then offer a metaethical explanation for why the counterexamples arise. Our explanation reveals a new and superior argument for two‐boxing, one that eschews the causal dominance principle in favor of a principle linking rational choice to guidance and actual value maximization

    High-Throughput Computing on High-Performance Platforms: A Case Study

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    The computing systems used by LHC experiments has historically consisted of the federation of hundreds to thousands of distributed resources, ranging from small to mid-size resource. In spite of the impressive scale of the existing distributed computing solutions, the federation of small to mid-size resources will be insufficient to meet projected future demands. This paper is a case study of how the ATLAS experiment has embraced Titan---a DOE leadership facility in conjunction with traditional distributed high- throughput computing to reach sustained production scales of approximately 52M core-hours a years. The three main contributions of this paper are: (i) a critical evaluation of design and operational considerations to support the sustained, scalable and production usage of Titan; (ii) a preliminary characterization of a next generation executor for PanDA to support new workloads and advanced execution modes; and (iii) early lessons for how current and future experimental and observational systems can be integrated with production supercomputers and other platforms in a general and extensible manner

    Migraine treatment tweak could reduce office visits

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    Add dexamethasone to the standard treatment of moderate to severe migraine headache; a single dose (8-24 mg) may prevent short-term recurrence, resulting in less need for medication and fewer repeat visits to the office or emergency department. Stength of recommendation: A: A meta-analysis

    Containers for Portable, Productive, and Performant Scientific Computing

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    Containers are an emerging technology that holds promise for improving productivity and code portability in scientific computing. The authors examine Linux container technology for the distribution of a nontrivial scientific computing software stack and its execution on a spectrum of platforms from laptop computers through high-performance computing systems. For Python code run on large parallel computers, the runtime is reduced inside a container due to faster library imports. The software distribution approach and data that the authors present will help developers and users decide on whether container technology is appropriate for them. The article also provides guidance for vendors of HPC systems that rely on proprietary libraries for performance on what they can do to make containers work seamlessly and without performance penalty

    H3K56me3 is a novel, conserved heterochromatic mark that largely but not completely overlaps with H3K9me3 in both regulation and localization.

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    Histone lysine (K) methylation has been shown to play a fundamental role in modulating chromatin architecture and regulation of gene expression. Here we report on the identification of histone H3K56, located at the pivotal, nucleosome DNA entry/exit point, as a novel methylation site that is evolutionary conserved. We identify trimethylation of H3K56 (H3K56me3) as a modification that is present during all cell cycle phases, with the exception of S-phase, where it is underrepresented on chromatin. H3K56me3 is a novel heterochromatin mark, since it is enriched at pericentromeres but not telomeres and is thereby similar, but not identical, to the localization of H3K9me3 and H4K20me3. Possibly due to H3 sequence similarities, Suv39h enzymes, responsible for trimethylation of H3K9, also affect methylation of H3K56. Similarly, we demonstrate that trimethylation of H3K56 is removed by members of the JMJD2 family of demethylases that also target H3K9me3. Furthermore, we identify and characterize mouse mJmjd2E and its human homolog hKDM4L as novel, functionally active enzymes that catalyze the removal of two methyl groups from trimethylated H3K9 and K56. H3K56me3 is also found in C. elegans, where it co-localizes with H3K9me3 in most, but not all, tissues. Taken together, our findings raise interesting questions regarding how methylation of H3K9 and H3K56 is regulated in different organisms and their functional roles in heterochromatin formation and/or maintenance
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