293 research outputs found
Maverick dark matter at colliders
Assuming that dark matter is a weakly interacting massive particle (WIMP)
species X produced in the early Universe as a cold thermal relic, we study the
collider signal of pp or ppbar -> XXbar + jets and its distinguishability from
standard-model background processes associated with jets and missing energy. We
assume that the WIMP is the sole particle related to dark matter within reach
of the LHC--a "maverick" particle--and that it couples to quarks through a
higher dimensional contact interaction. We simulate the WIMP final-state signal
XXbar + jet and dominant standard-model (SM) background processes and find that
the dark-matter production process results in higher energies for the colored
final state partons than do the standard-model background processes, resulting
in more QCD radiation and a higher jet multiplicity. As a consequence, the
detectable signature of maverick dark matter is an excess over standard-model
expectations of events consisting of large missing transverse energy, together
with large leading jet transverse momentum and scalar sum of the transverse
momenta of the jets. Existing Tevatron data and forthcoming LHC data can
constrain (or discover!) maverick dark matter.Comment: 11 pages, 7 figure
The impact of heavy-quark loops on LHC dark matter searches
If only tree-level processes are included in the analysis, LHC monojet
searches give weak constraints on the dark matter-proton scattering cross
section arising from the exchange of a new heavy scalar or pseudoscalar
mediator with Yukawa-like couplings to quarks. In this letter we calculate the
constraints on these interactions from the CMS 5.0/fb and ATLAS 4.7/fb searches
for jets with missing energy including the effects of heavy-quark loops. We
find that the inclusion of such contributions leads to a dramatic increase in
the predicted cross section and therefore a significant improvement of the
bounds from LHC searches.Comment: 12 pages, 1 table, 3 figures, v2: extended discussion and improved
relic density calculation - matches published versio
El suicidio en Segovia (1992-1994).
Se registran los suicidios consumados, y las tentativas de suicidio que ingresaron en el Hospital General de Segovia entre 1992 y 1994. La tasa media anual de suicidios consumados es de 9,3 por diez mil habitantes y la de tentativas de 29,5, muy distintas a las recogidas en la Estadística del Suicidio del INE. Se establecen diferencias entre el suicidio consumado, suicidio frustrado y tentativas de suicidio (parasuicidio) considerando algunos factores asociados a las distintas conductas suicidas
El suicidio en Segovia (1992-1994).
Se registran los suicidios consumados, y las tentativas de suicidio que ingresaron en el Hospital General de Segovia entre 1992 y 1994. La tasa media anual de suicidios consumados es de 9,3 por diez mil habitantes y la de tentativas de 29,5, muy distintas a las recogidas en la Estadística del Suicidio del INE. Se establecen diferencias entre el suicidio consumado, suicidio frustrado y tentativas de suicidio (parasuicidio) considerando algunos factores asociados a las distintas conductas suicidas
Dark Matter from Minimal Flavor Violation
We consider theories of flavored dark matter, in which the dark matter
particle is part of a multiplet transforming nontrivially under the flavor
group of the Standard Model in a manner consistent with the principle of
Minimal Flavor Violation (MFV). MFV automatically leads to the stability of the
lightest state for a large number of flavor multiplets. If neutral, this
particle is an excellent dark matter candidate. Furthermore, MFV implies
specific patterns of mass splittings among the flavors of dark matter and
governs the structure of the couplings between dark matter and ordinary
particles, leading to a rich and predictive cosmology and phenomenology. We
present an illustrative phenomenological study of an effective theory of a
flavor SU(3)_Q triplet, gauge singlet scalar.Comment: 10 pages, 2 figures; v2: references added, minor changes to collider
analysis, conclusions unchange
Diagnostic accuracy of white cell count and C-reactive protein for assessing the severity of paediatric appendicitis
Closing in on Asymmetric Dark Matter I: Model independent limits for interactions with quarks
It is argued that experimental constraints on theories of asymmetric dark
matter (ADM) almost certainly require that the DM be part of a richer hidden
sector of interacting states of comparable mass or lighter. A general requisite
of models of ADM is that the vast majority of the symmetric component of the DM
number density must be removed in order to explain the observed relationship
via the DM asymmetry. Demanding the efficient
annihilation of the symmetric component leads to a tension with experimental
limits if the annihilation is directly to Standard Model (SM) degrees of
freedom. A comprehensive effective operator analysis of the model independent
constraints on ADM from direct detection experiments and LHC monojet searches
is presented. Notably, the limits obtained essentially exclude models of ADM
with mass 1GeV 100GeV annihilating to SM quarks via
heavy mediator states. This motivates the study of portal interactions between
the dark and SM sectors mediated by light states. Resonances and threshold
effects involving the new light states are shown to be important for
determining the exclusion limits.Comment: 18+6 pages, 18 figures. v2: version accepted for publicatio
Walker-Warburg syndrome
Walker-Warburg Syndrome (WWS) is a rare form of autosomal recessive congenital muscular dystrophy associated with brain and eye abnormalities. WWS has a worldwide distribution. The overall incidence is unknown but a survey in North-eastern Italy has reported an incidence rate of 1.2 per 100,000 live births. It is the most severe form of congenital muscular dystrophy with most children dying before the age of three years. WWS presents at birth with generalized hypotonia, muscle weakness, developmental delay with mental retardation and occasional seizures. It is associated with type II cobblestone lissencephaly, hydrocephalus, cerebellar malformations, eye abnormalities and congenital muscular dystrophy characterized by hypoglycosylation of α-dystroglycan. Several genes have been implicated in the etiology of WWS, and others are as yet unknown. Several mutations were found in the Protein O-Mannosyltransferase 1 and 2 (POMT1 and POMT2) genes, and one mutation was found in each of the fukutin and fukutin-related protein (FKRP) genes. Laboratory investigations usually show elevated creatine kinase, myopathic/dystrophic muscle pathology and altered α-dystroglycan. Antenatal diagnosis is possible in families with known mutations. Prenatal ultrasound may be helpful for diagnosis in families where the molecular defect is unknown. No specific treatment is available. Management is only supportive and preventive
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