95 research outputs found
The fine-tuning price of the early LHC
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
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
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
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
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
125 GeV Higgs Boson from t-b-tau Yukawa Unification
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
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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