119 research outputs found

    Cosmology: The Noncommutative Quantum and Classical Cosmology

    Get PDF

    Analysis of Scalar Field Cosmology with Phase Space Deformations

    Get PDF
    Phase space deformations on scalar field cosmology are studied. The deformation is introduced by modifying the symplectic structure of the minisuperspace variables. The effects of the deformation are studied in the “C-frame” and the “NC-frame.” In order to remove the ambiguities of working on different frames, a new principle is introduced. When we impose that both frames should be physically equivalent, we conclude that the only possibility for this model, is to have an effective cosmological constant Λeff≥0. Finally we bound the parameter space for θ and β

    WKB-type Approximation to Noncommutative Quantum Cosmology

    Get PDF
    In this work, we develop and apply the WKB approximation to several examples of noncommutative quantum cosmology, obtaining the time evolution of the noncommutative universe, this is done starting from a noncommutative quantum formulation of cosmology where the noncommutativity is introduced by a deformation on the minisuperspace variables. This procedure gives a straightforward algorithm to incorporate noncommutativity to cosmology and inflation.Comment: Revtex4, 6 pages, no figure

    Phase Transition in Liquid Drop Fragmentation

    Full text link
    A liquid droplet is fragmented by a sudden pressurized-gas blow, and the resulting droplets, adhered to the window of a flatbed scanner, are counted and sized by computerized means. The use of a scanner plus image recognition software enables us to automatically count and size up to tens of thousands of tiny droplets with a smallest detectable volume of approximately 0.02 nl. Upon varying the gas pressure, a critical value is found where the size-distribution becomes a pure power-law, a fact that is indicative of a phase transition. Away from this transition, the resulting size distributions are well described by Fisher's model at coexistence. It is found that the sign of the surface correction term changes sign, and the apparent power-law exponent tau has a steep minimum, at criticality, as previously reported in Nuclear Multifragmentation studies [1,2]. We argue that the observed transition is not percolative, and introduce the concept of dominance in order to characterize it. The dominance probability is found to go to zero sharply at the transition. Simple arguments suggest that the correlation length exponent is nu=1/2. The sizes of the largest and average fragments, on the other hand, do not go to zero but behave in a way that appears to be consistent with recent predictions of Ashurst and Holian [3,4].Comment: 10 pages, 11 figures. LaTeX (revtex4) with psfig/epsfi

    Proteomic profiling reveals mitochondrial dysfunction in the cerebellum of transgenic mice overexpressing DYRK1A, a Down syndrome candidate gene

    Full text link
    DYRK1A is a dual-specificity kinase that is overexpressed in Down syndrome (DS) and plays a key role in neurogenesis, neuronal differentiation and function, cognitive phenotypes, and aging. Dyrk1A has also been implicated in cerebellar abnormalities observed in association with DS, and normalization of Dyrk1A dosage rescues granular and Purkinje cell densities in a trisomic DS mouse model. However, the underlying molecular mechanisms governing these processes are unknown.To shed light on the effects of Dyrk1A overexpression in the cerebellum, here we investigated the cerebellar proteome in transgenic Dyrk1A overexpressing mice in basal conditions and after treatment with green tea extract containing epigallocatechin-3-gallate (EGCG), a DYRK1A inhibitor.Our results showed that Dyrk1A overexpression alters oxidative phosphorylation and mitochondrial function in the cerebellum of transgenic mice. These alterations are significantly rescued upon EGCG-containing green tea extract treatment, suggesting that its effects in DS could depend in part on targeting mitochondria, as shown by the partially restoration by the treatment of the increased mtDNA copy number in TG non-treated mice.Copyright © 2022 De Toma, Ortega, Fernández-Blanco, Calderón, Barahona, Trullàs, Sabidó and Dierssen
    corecore