95 research outputs found

    The fine-tuning price of the early LHC

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    LHC already probed and excluded half of the parameter space of the Constrained Minimal Supersymmetric Standard Model allowed by previous experiments. Only about 0.3% of the CMSSM parameter space survives. This fraction rises to about 0.9% if the bound on the Higgs mass can be circumvented.Comment: 7 pages. v3: updated with new bounds from ATLAS and CMS at 1.1/fb presented at the EPS-HEP-2011 conferenc

    Naturalness and Fine Tuning in the NMSSM: Implications of Early LHC Results

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    We study the fine tuning in the parameter space of the semi-constrained NMSSM, where most soft Susy breaking parameters are universal at the GUT scale. We discuss the dependence of the fine tuning on the soft Susy breaking parameters M_1/2 and m0, and on the Higgs masses in NMSSM specific scenarios involving large singlet-doublet Higgs mixing or dominant Higgs-to-Higgs decays. Whereas these latter scenarios allow a priori for considerably less fine tuning than the constrained MSSM, the early LHC results rule out a large part of the parameter space of the semi-constrained NMSSM corresponding to low values of the fine tuning.Comment: 19 pages, 10 figures, bounds from Susy searches with ~1/fb include

    Yukawa unification in SO(10) with light sparticle spectrum

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    We investigate supersymmetric SO(10) GUT model with \mu<0. The requirements of top-bottom-tau Yukawa unification, correct radiative electroweak symmetry breaking and agreement with the present experimental data may be met when the soft masses of scalars and gauginos are non-universal. We show how appropriate non-universalities can easily be obtained in the SO(10) GUT broken to the Standard Model. We discuss how values of BR(b-->s \gamma) and (g-2)_\mu simultaneously in a good agreement with the experimental data can be achieved in SO(10) model with \mu<0. In the region of the parameter space preferred by our analysis there are two main mechanisms leading to the LSP relic abundance consistent with the WMAP results. One is the co-annihilation with the stau and the second is the resonant annihilation via exchange of the Z boson or the light Higgs scalar. A very interesting feature of SO(10) models with negative \mu is that they predict relatively light sparticle spectra. Even the heaviest superpartners may easily have masses below 1.5 TeV in contrast to multi-TeV particles typical for models with positive \mu.Comment: 23 pages, 5 figure

    Light dark matter in the NMSSM: upper bounds on direct detection cross sections

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    In the Next-to-Minimal Supersymmetric Standard Model, a bino-like LSP can be as light as a few GeV and satisfy WMAP constraints on the dark matter relic density in the presence of a light CP-odd Higgs scalar. We study upper bounds on the direct detection cross sections for such a light LSP in the mass range 2-20 GeV in the NMSSM, respecting all constraints from B-physics and LEP. The OPAL constraints on e^+ e^- -> \chi^0_1 \chi^0_i (i > 1) play an important role and are discussed in some detail. The resulting upper bounds on the spin-independent and spin-dependent nucleon cross sections are ~ 10^{-42} cm^{-2} and ~ 4\times 10^{-40} cm^{-2}, respectively. Hence the upper bound on the spin-independent cross section is below the DAMA and CoGeNT regions, but could be compatible with the two events observed by CDMS-II.Comment: 17 pages, 3 figure

    Excluding Electroweak Baryogenesis in the MSSM

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    In the context of the MSSM the Light Stop Scenario (LSS) is the only region of parameter space that allows for successful Electroweak Baryogenesis (EWBG). This possibility is very phenomenologically attractive, since it allows for the direct production of light stops and could be tested at the LHC. The ATLAS and CMS experiments have recently supplied tantalizing hints for a Higgs boson with a mass of ~ 125 GeV. This Higgs mass severely restricts the parameter space of the LSS, and we discuss the specific predictions made for EWBG in the MSSM. Combining data from all the available ATLAS and CMS Higgs searches reveals a tension with the predictions of EWBG even at this early stage. This allows us to exclude EWBG in the MSSM at greater than (90) 95% confidence level in the (non-)decoupling limit, by examining correlations between different Higgs decay channels. We also examine the exclusion without the assumption of a ~ 125 GeV Higgs. The Higgs searches are still highly constraining, excluding the entire EWBG parameter space at greater than 90% CL except for a small window of m_h ~ 117 - 119 GeV.Comment: 24 Pages, 4 Figures (v3: fixed typos, minor corrections, added references

    Search for the standard model Higgs boson at LEP

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    125 GeV Higgs Boson from t-b-tau Yukawa Unification

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    We identify a class of supersymmetric SU(4)_c x SU(2)_L x SU(2)_R models in which imposing essentially perfect t-b-tau Yukawa coupling unification at M_GUT yields a mass close to 122-126 GeV for the lightest CP-even (SM-like) Higgs boson. The squark and gluino masses in these models exceed 3 TeV, but the stau and charginos in some cases can be considerably lighter. We display some benchmark points corresponding to neutralino-stau and bino-wino coannihilations as well as A-resonance. The well-known MSSM parameter tan beta is around 46-52.Comment: 16 pages, 4 figure

    Rotavirus A genotype G1P[8]: a novel method to distinguish wild-type strains from the Rotarix® vaccine strain

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    Rotaviruses are important enteric pathogens for humans and animals. Group A rotaviruses (RV-A) are the most common agents of severe gastroenteritis in infants and young children and vaccination is the most effective method to reduce RV-A-associated diseases. G1P[8], the most prevalent RV-A genotype worldwide, is included in the RV-A vaccine Rotarix®. The discrimination between wild-type G1P[8] and vaccine G1P[8] strains is an important topic in the study of RV-A epidemiology to manage outbreaks and to define control measures for vaccinated children. In this study, we developed a novel method to segregate the wild-type and vaccine strains using restriction endonucleases. The dsRNA from the Rotarix® vaccine was sequenced and the NSP3 gene was selected as the target gene. The vaccine strain has a restriction pattern that is different than that of wild-type RV-A G1P[8] isolates after digestion with the restriction endonuclease BspHI. This pattern could be used as a marker for the differentiation of wild-type G1P[8] strains from the vaccine strain
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