546 research outputs found

    Bell's Theorem and Nonlinear Systems

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    For all Einstein-Podolsky-Rosen-type experiments on deterministic systems the Bell inequality holds, unless non-local interactions exist between certain parts of the setup. Here we show that in nonlinear systems the Bell inequality can be violated by non-local effects that are arbitrarily weak. Then we show that the quantum result of the existing Einstein-Podolsky-Rosen-type experiments can be reproduced within deterministic models that include arbitrarily weak non-local effects.Comment: Accepted for publication in Europhysics Letters. 14 pages, no figures. In the Appendix (not included in the EPL version) the author says what he really thinks about the subjec

    Depletion-mode Quantum Dots in Intrinsic Silicon

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    We report the fabrication and electrical characterization of depletion-mode quantum dots in a two-dimensional hole gas (2DHG) in intrinsic silicon. We use fixed charge in a SiO2_2/Al2_2O3_3 dielectric stack to induce a 2DHG at the Si/SiO2_2 interface. Fabrication of the gate structures is accomplished with a single layer metallization process. Transport spectroscopy reveals regular Coulomb oscillations with charging energies of 10-15 meV and 3-5 meV for the few- and many-hole regimes, respectively. This depletion-mode design avoids complex multilayer architectures requiring precision alignment, and allows to adopt directly best practices already developed for depletion dots in other material systems. We also demonstrate a method to deactivate fixed charge in the SiO2_2/Al2_2O3_3 dielectric stack using deep ultraviolet light, which may become an important procedure to avoid unwanted 2DHG build-up in Si MOS quantum bits.Comment: Accepted to Applied Physics Letters. 5 pages, 3 figure

    <i>atonal-</i> and <i>achaete-scute</i>-related genes in the annelid <i>Platynereis dumerilii</i>: insights into the evolution of neural basic-Helix-Loop-Helix genes

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    Background: Functional studies in model organisms, such as vertebrates and Drosophila, have shown that basic Helix-loop-Helix ( bHLH) proteins have important roles in different steps of neurogenesis, from the acquisition of neural fate to the differentiation into specific neural cell types. However, these studies highlighted many differences in the expression and function of orthologous bHLH proteins during neural development between vertebrates and Drosophila. To understand how the functions of neural bHLH genes have evolved among bilaterians, we have performed a detailed study of bHLH genes during nervous system development in the polychaete annelid, Platynereis dumerilii, an organism which is evolutionary distant from both Drosophila and vertebrates. Results: We have studied Platynereis orthologs of the most important vertebrate neural bHLH genes, i.e. achaete-scute, neurogenin, atonal, olig, and NeuroD genes, the latter two being genes absent of the Drosophila genome. We observed that all these genes have specific expression patterns during nervous system formation in Platynereis. Our data suggest that in Platynereis, like in vertebrates but unlike Drosophila, ( i) neurogenin is the main proneural gene for the formation of the trunk central nervous system, (ii) achaetescute and olig genes are involved in neural subtype specification in the central nervous system, in particular in the specification of the serotonergic phenotype. In addition, we found that the Platynereis NeuroD gene has a broad and early neuroectodermal expression, which is completely different from the neuronal expression of vertebrate NeuroD genes. Conclusion: Our analysis suggests that the Platynereis bHLH genes have both proneural and neuronal specification functions, in a way more akin to the vertebrate situation than to that of Drosophila. We conclude that these features are ancestral to bilaterians and have been conserved in the vertebrates and annelids lineages, but have diverged in the evolutionary lineage leading to Drosophila

    Origin and evolution of the Notch signalling pathway: an overview from eukaryotic genomes

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    Background. Of the 20 or so signal transduction pathways that orchestrate cell-cell interactions in metazoans, seven are involved during development. One of these is the Notch signalling pathway which regulates cellular identity, proliferation, differentiation and apoptosis via the developmental processes of lateral inhibition and boundary induction. In light of this essential role played in metazoan development, we surveyed a wide range of eukaryotic genomes to determine the origin and evolution of the components and auxiliary factors that compose and modulate this pathway. Results. We searched for 22 components of the Notch pathway in 35 different species that represent 8 major clades of eukaryotes, performed phylogenetic analyses and compared the domain compositions of the two fundamental molecules: the receptor Notch and its ligands Delta/Jagged. We confirm that a Notch pathway, with true receptors and ligands is specific to the Metazoa. This study also sheds light on the deep ancestry of a number of genes involved in this pathway, while other members are revealed to have a more recent origin. The origin of several components can be accounted for by the shuffling of pre-existing protein domains, or via lateral gene transfer. In addition, certain domains have appeared de novo more recently, and can be considered metazoan synapomorphies. Conclusion. The Notch signalling pathway emerged in Metazoa via a diversity of molecular mechanisms, incorporating both novel and ancient protein domains during eukaryote evolution. Thus, a functional Notch signalling pathway was probably present in Urmetazoa

    Separation of the guajira-bonaire pair: 65-50ma exhumation followed by 300 km right-lateral transtensional deformation

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    Zapata, S.1, Cardona, A.2, Montes, C3, Valencia, V.4, Vervoort, J.4 and amp; Reiners, P.5 1 Corporación Geológica Ares, Calle 57 No. 23-09 of 202, Bogotá, Colombia. [email protected] 2 Departamento de Procesos y Energía, Universidad Nacional de Colombia Sede Medellín, Medellín, Colombia [email protected] 3 Geociencias, Universidad de Los Andes, Departamento de Geología, Bogotá, Colombia. 4 School of Earth and Environmental Sciences, Washington State University, Pullman, USA 5Department of Geosciences, University of Arizona, Tucson, USA Upper Eocene fluvial strata in the Island of Bonaire contain detrital components that were tracked to the basement massifs of the Guajira Peninsula in northern of Colombia. These components confirm previous hypothesis that the Guajira-Bonaire pair constitute a tectonic piercing point along the southern Caribbean Plate margin that was right-laterally displaced approximately 300km after middle Eocene times. Other possible sources, the nearby Curaҫao and the far away Santa Marta Massif, did not pass statistical similarity and overlap tests. U-Pb LA-ICP-MS from the metamorphic boulders of the Soebi Blanco Formation in Bonaire yields Grenvillian ages (1084Ma, 1130Ma and 1184Ma), while the detrital zircons recovered from the sandy matrix of the conglomerates contain populations with peaks of 1000 - 1200Ma, 750 - 950Ma and 200 – 300 Ma. Overlap and similarity tests run between these populations and published data from Guajira yield values of 0.750 and 0.680, which are significantly higher than the same comparison against the Santa Marta Massif (0.637 and 0.522), and the Curaҫao Island (0.629 and 0.467). Thermogeochronological results from the metamorphic clasts yield Paleocene-middle Eocene ages (65 – 50Ma) that confirm not only a regional-scale cooling event in this time period, but also help constrain the maximum depositional age (50Ma) of the poorly dated Soebi Blanco Formation

    Dynamic Interpretation of Hedgehog Signaling in the Drosophila Wing Disc

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    Morphogens are classically defined as molecules that control patterning by acting at a distance to regulate gene expression in a concentration-dependent manner. In the Drosophila wing imaginal disc, secreted Hedgehog (Hh) forms an extracellular gradient that organizes patterning along the anterior–posterior axis and specifies at least three different domains of gene expression. Although the prevailing view is that Hh functions in the Drosophila wing disc as a classical morphogen, a direct correspondence between the borders of these patterns and Hh concentration thresholds has not been demonstrated. Here, we provide evidence that the interpretation of Hh signaling depends on the history of exposure to Hh and propose that a single concentration threshold is sufficient to support multiple outputs. Using mathematical modeling, we predict that at steady state, only two domains can be defined in response to Hh, suggesting that the boundaries of two or more gene expression patterns cannot be specified by a static Hh gradient. Computer simulations suggest that a spatial “overshoot” of the Hh gradient occurs, i.e., a transient state in which the Hh profile is expanded compared to the Hh steady-state gradient. Through a temporal examination of Hh target gene expression, we observe that the patterns initially expand anteriorly and then refine, providing in vivo evidence for the overshoot. The Hh gene network architecture suggests this overshoot results from the Hh-dependent up-regulation of the receptor, Patched (Ptc). In fact, when the network structure was altered such that the ptc gene is no longer up-regulated in response to Hh-signaling activation, we found that the patterns of gene expression, which have distinct borders in wild-type discs, now overlap. Our results support a model in which Hh gradient dynamics, resulting from Ptc up-regulation, play an instructional role in the establishment of patterns of gene expression

    The muscle metabolome differs between healthy and frail older adults

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    Populations around the world are aging rapidly. Age-related loss of physiological functions negatively affects quality of life. A major contributor to the frailty syndrome of aging is loss of skeletal muscle. In this study we assessed the skeletal muscle biopsy metabolome of healthy young, healthy older and frail older subjects to determine the effect of age and frailty on the metabolic signature of skeletal muscle tissue. In addition, the effects of prolonged whole-body resistance-type exercise training on the muscle metabolome of older subjects were examined. The baseline metabolome was measured in muscle biopsies collected from 30 young, 66 healthy older subjects and 43 frail older subjects. Follow-up samples from frail older (24 samples) and healthy older subjects (38 samples) were collected after 6 months of prolonged resistance-type exercise training. Young subjects were included as a reference If thisgroup. Primary differences in skeletal muscle metabolite levels between young and healthy older subjects were related to mitochondrial function, muscle fiber type, and tissue turnover. Similar differences were observed when comparing frail older subjects with healthy older subjects at baseline. Prolonged resistance-type exercise training resulted in an adaptive response of amino acid metabolism, especially reflected in branched chain amino acids and genes related to tissue remodeling. The effect of exercise training on branched-chain amino acid-derived acylcarnitines in older subjects points to a downward shift in branched-chain amino acid catabolism upon training. We observed only modest correlations between muscle and plasma metabolite levels, which pleads against the use of plasma metabolites as a direct read-out of muscle metabolism and stresses the need for direct assessment of metabolites in muscle tissue biopsies
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