Gravitino Dark Matter in the CMSSM With Improved Constraints from BBN

In the framework of the Constrained MSSM we re--examine the gravitino as the lightest superpartner and a candidate for cold dark matter in the Universe. Unlike in other recent studies, we include both a thermal contribution to its relic population from scatterings in the plasma and a non--thermal one from neutralino or stau decays after freeze--out. Relative to a previous analysis [1] we update, extend and considerably improve our treatment of constraints from observed light element abundances on additional energy released during BBN in association with late gravitino production. Assuming the gravitino mass in the GeV to TeV range, and for natural ranges of other supersymmetric parameters, the neutralino region is excluded, while for smaller values of the gravitino mass it becomes allowed again. The gravitino relic abundance is consistent with observational constraints on cold dark matter from BBN and CMB in some well defined domains of the stau region but, in most cases, only due to a dominant contribution of the thermal population. This implies, depending on the gravitino mass, a large enough reheating temperature. If \mgravitino>1 GeV then $T_R>10^7$ GeV, if allowed by BBN and other constraints but, for light gravitinos, if \mgravitino>100 keV then $T_R>3\times 10^3$ GeV. On the other hand, constraints mostly from BBN imply an upper bound T_R \lsim {a few}x 10^8\times10^9 GeV which appears inconsistent with thermal leptogenesis. Finally, most of the preferred stau region corresponds to the physical vacuum being a false vacuum. The scenario can be partially probed at the LHC.Comment: Version with Erratum. Numerical bug fixed. An upper bound on the reheating temperature strengthened by about an order of magnitud

Measuring the Sterile Neutrino Mass in Spallation Source and Direct Detection Experiments

We explore the complementarity of direct detection (DD) and spallation source (SS) experiments for the study of sterile neutrino physics. We focus on the sterile baryonic neutrino model: an extension of the Standard Model that introduces a massive sterile neutrino with couplings to the quark sector via a new gauge boson. In this scenario, the inelastic scattering of an active neutrino with the target material in both DD and SS experiments gives rise to a characteristic nuclear recoil energy spectrum that can allow for the reconstruction of the neutrino mass in the event of a positive detection. We first derive new bounds on this model based on the data from the COHERENT collaboration on CsI and LAr targets, which we find do not yet probe new areas of the parameter space. We then assess how well future SS experiments will be able to measure the sterile neutrino mass and mixings, showing that masses in the range 15-50 MeV can be reconstructed. We show that there is a degeneracy in the measurement of the sterile neutrino mixing that substantially affects the reconstruction of parameters for masses of the order of 40 MeV. Thanks to their lower energy threshold and sensitivity to the solar tau neutrino flux, DD experiments allow us to partially lift the degeneracy in the sterile neutrino mixings and considerably improve its mass reconstruction down to 9 MeV. Our results demonstrate the excellent complementarity between DD and SS experiments in measuring the sterile neutrino mass and highlight the power of DD experiments in searching for new physics in the neutrino sector.Comment: 22 pages, 10 figure

Presence of Middle Cerebellar Peduncle Sign in FMR1 Premutation Carriers Without Tremor and Ataxia

Here we report five cases of male FMR1 premutation carriers who present without clinical symptoms of the fragile X-associated tremor/ataxia syndrome (FXTAS), but who on MRI demonstrate white matter hyperintensities in the middle cerebellar peduncles (MCP sign) and other brain regions, a rare finding. MCP sign is the major radiological feature of FXTAS; it is therefore remarkable to identify five cases in which this MRI finding is present in the absence of tremor and ataxia, the major clinical features of FXTAS. Subjects underwent a detailed neurological evaluation, neuropsychological testing, molecular testing, and MRI evaluation utilizing T2 imaging described here. Additional white matter disease was present in the corpus callosum in four of the five cases. However, all cases were asymptomatic for motor signs of FXTAS

Expansion of the Protein Repertoire in Newly Explored Environments: Human Gut Microbiome Specific Protein Families

The microbes that inhabit particular environments must be able to perform molecular functions that provide them with a competitive advantage to thrive in those environments. As most molecular functions are performed by proteins and are conserved between related proteins, we can expect that organisms successful in a given environmental niche would contain protein families that are specific for functions that are important in that environment. For instance, the human gut is rich in polysaccharides from the diet or secreted by the host, and is dominated by Bacteroides, whose genomes contain highly expanded repertoire of protein families involved in carbohydrate metabolism. To identify other protein families that are specific to this environment, we investigated the distribution of protein families in the currently available human gut genomic and metagenomic data. Using an automated procedure, we identified a group of protein families strongly overrepresented in the human gut. These not only include many families described previously but also, interestingly, a large group of previously unrecognized protein families, which suggests that we still have much to discover about this environment. The identification and analysis of these families could provide us with new information about an environment critical to our health and well being

c- and N-myc Regulate Neural Precursor Cell Fate, Cell Cycle, and Metabolism to Direct Cerebellar Development

Separate murine knockout (KO) of either c- or N-myc genes in neural stem and precursor cells (NSC) driven by nestin-cre causes microcephaly. The cerebellum is particularly affected in the N-myc KO, leading to a strong reduction in cerebellar granule neural progenitors (CGNP) and mature granule neurons. In humans, mutation of N-myc also causes microcephaly in Feingold Syndrome. We created a double KO (DKO) of c- and N-myc using nestin-cre, which strongly impairs brain growth, particularly that of the cerebellum. Granule neurons were almost absent from the Myc DKO cerebellum, and other cell types were relatively overrepresented, including astroglia, oligodendrocytes, and Purkinje neurons. These findings are indicative of a profound disruption of cell fate of cerebellar stem and precursors. DKO Purkinje neurons were strikingly lacking in normal arborization. Inhibitory neurons were ectopic and exhibited very abnormal GAD67 staining patterns. Also consistent with altered cell fate, the adult DKO cerebellum still retained a residual external germinal layer (EGL). CGNP in the DKO EGL were almost uniformly NeuN and p27KIP1 positive as well as negative for Math1 and BrdU at the peak of normal cerebellar proliferation at P6. The presence of some mitotic CGNP in the absence of S phase cells suggests a possible arrest in M phase. CGNP and NSC metabolism also was affected by loss of Myc as DKO cells exhibited weak nucleolin staining. Together these findings indicate that c- and N-Myc direct cerebellar development by maintaining CGNP and NSC populations through inhibiting differentiation as well as directing rapid cell cycling and active cellular metabolism