1,125 research outputs found

    Shallow foundations for the support of vertical-wall bridge abutments: interaction between riprap and contraction scour

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    The database from flume experiments focused on the performance of riprap layouts based on field installations and FHWA HEC-23 design guidelines against clear-water abutment scour combined with Computational Fluid Dynamics (CFD) is used to investigate how flow fields at single span bridge openings, dominated by flow contraction, adjust in response to variations of bed roughness and cross-section geometry due to riprap installations. These adjustments increase bed shear stress magnitudes on the unprotected erodible bed leading to underestimated contraction scour depths therefore creating instability, and ultimately causing edge failure of the riprap. Based on the combined physical/numerical modeling approach an edge failure-resistant riprap layout is proposed. Furthermore, the CFD approach provides an insight into shear stress magnitudes within a nonuniform bed roughness in the bridge opening, and a comprehensive flowdepth-riprap interaction model to define limits for “hydraulically narrow” bridge openings that might be prone to edge failure of the scour protecting riprap

    A Nonabelian Yang-Mills Analogue of Classical Electromagnetic Duality

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    The classic question of a nonabelian Yang-Mills analogue to electromagnetic duality is here examined in a minimalist fashion at the strictly 4-dimensional, classical field and point charge level. A generalisation of the abelian Hodge star duality is found which, though not yet known to give dual symmetry, reproduces analogues to many dual properties of the abelian theory. For example, there is a dual potential, but it is a 2-indexed tensor TΌΜT_{\mu\nu} of the Freedman-Townsend type. Though not itself functioning as such, TΌΜT_{\mu\nu} gives rise to a dual parallel transport, A~ÎŒ\tilde{A}_\mu, for the phase of the wave function of the colour magnetic charge, this last being a monopole of the Yang-Mills field but a source of the dual field. The standard colour (electric) charge itself is found to be a monopole of A~ÎŒ\tilde{A}_\mu. At the same time, the gauge symmetry is found doubled from say SU(N)SU(N) to SU(N)×SU(N)SU(N) \times SU(N). A novel feature is that all equations of motion, including the standard Yang-Mills and Wong equations, are here derived from a `universal' principle, namely the Wu-Yang (1976) criterion for monopoles, where interactions arise purely as a consequence of the topological definition of the monopole charge. The technique used is the loop space formulation of Polyakov (1980).Comment: We regret that, due to a technical hitch, parts of the reference list were mixed up. This is the corrected version. We apologize to the authors whose papers were misquote

    A computational approach to the study of the stability of pier riprap at the Middle Fork Feather River

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    This paper discusses the use of various technologies and advanced computational modeling techniques that were combined for monitoring the performance of pier riprap on the basis of a field case study – Pier 3 of a bridge over the Middle Fork Feather River – in northern California, USA. The first phase involved capturing the field condition of the bridge site using sonar instrumentation technology in order to obtain high resolution bathymetry data. The second phase entailed enhancement and transformation of the scanned bathymetric data into a 3D CAD model to be used as the initial geometry for numerical modeling. A Fluid Structure Interaction (FSI) numerical approach was applied to simulate the rock incipient motion i.e. shear failure by coupling Computational Fluid Dynamics (CFD) software STAR-CCM+ and a Computational Structural Mechanics (CSM) software LS-DYNA. Several coupled simulations have been performed with varying flow conditions to identify shear failure conditions for the riprap apron

    The LKB1-salt-inducible kinase pathway functions as a key gluconeogenic suppressor in the liver

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    LKB1 is a master kinase that regulates metabolism and growth through adenosine monophosphate-activated protein kinase (AMPK) and 12 other closely related kinases. Liver-specific ablation of LKB1 causes increased glucose production in hepatocytes in vitro and hyperglycaemia in fasting mice in vivo. Here we report that the salt-inducible kinases (SIK1, 2 and 3), members of the AMPK-related kinase family, play a key role as gluconeogenic suppressors downstream of LKB1 in the liver. The selective SIK inhibitor HG-9-91-01 promotes dephosphorylation of transcriptional co-activators CRTC2/3 resulting in enhanced gluconeogenic gene expression and glucose production in hepatocytes, an effect that is abolished when an HG-9-91-01-insensitive mutant SIK is introduced or LKB1 is ablated. Although SIK2 was proposed as a key regulator of insulin-mediated suppression of gluconeogenesis, we provide genetic evidence that liver-specific ablation of SIK2 alone has no effect on gluconeogenesis and insulin does not modulate SIK2 phosphorylation or activity. Collectively, we demonstrate that the LKB1-SIK pathway functions as a key gluconeogenic gatekeeper in the liver

    Cognitive impairment induced by delta9-tetrahydrocannabinol occurs through heteromers between cannabinoid CB1 and serotonin 5-HT2A receptors

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    Delta-9-tetrahydrocannabinol (THC), the main psychoactive compound of marijuana, induces numerous undesirable effects, including memory impairments, anxiety, and dependence. Conversely, THC also has potentially therapeutic effects, including analgesia, muscle relaxation, and neuroprotection. However, the mechanisms that dissociate these responses are still not known. Using mice lacking the serotonin receptor 5-HT2A, we revealed that the analgesic and amnesic effects of THC are independent of each other: while amnesia induced by THC disappears in the mutant mice, THC can still promote analgesia in these animals. In subsequent molecular studies, we showed that in specific brain regions involved in memory formation, the receptors for THC and the 5-HT2A receptors work together by physically interacting with each other. Experimentally interfering with this interaction prevented the memory deficits induced by THC, but not its analgesic properties. Our results highlight a novel mechanism by which the beneficial analgesic properties of THC can be dissociated from its cognitive side effects

    UGT2B17 Genetic Polymorphisms Dramatically Affect the Pharmacokinetics of MK-7246 in Healthy Subjects in a First-in-Human Study

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    MK-7246, an antagonist of the chemoattractant receptor on T helper type 2 (Th2) cells, is being developed for the treatment of respiratory diseases. In a first-in-human study, we investigated whether genetic polymorphisms contributed to the marked intersubject variability in the pharmacokinetics of MK-7246 and its glucuronide metabolite M3. Results from in vitro enzyme kinetic studies suggested that UGT2B17 is probably the major enzyme responsible for MK-7246 metabolism in both the liver and the intestine. As compared with those with the UGT2B17*1/*1 wild-type genotype, UGT2B17*2/*2 carriers, who possess no UGT2B17 protein, had 25- and 82-fold greater mean dose-normalized values of area under the plasma concentration–time curve (AUC) and peak concentration of MK-7246, respectively, and a 24-fold lower M3-to-MK-7246 AUC ratio. The apparent half-life of MK-7246 was not as variable between these two genotypes. Therefore, the highly variable pharmacokinetics of MK-7246 is attributable primarily to the impact of UGT2B17 genetic polymorphisms and extensive first-pass metabolism of MK-7246

    Control of daughter centriole formation by the pericentriolar material

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    Author Posting. © The Author(s), 2008. This is the author's version of the work. It is posted here by permission of Nature Publishing Group for personal use, not for redistribution. The definitive version was published in Nature Cell Biology 10 (2008): 322-328, doi:10.1038/ncb1694.Controlling the number of its centrioles is vital for the cell as supernumerary centrioles result in multipolar mitosis and genomic instability. Normally, just one daughter centriole forms on each mature (mother) centriole; however, a mother centriole can produce multiple daughters within a single cell cycle. The mechanisms that prevent centriole ‘overduplication’ are poorly understood. Here we use laser microsurgery to test the hypothesis that attachment of the daughter centriole to the wall of the mother inhibits formation of additional daughters. We show that physical removal of the daughter induces reduplication of the mother in Sarrested cells. Under conditions when multiple daughters simultaneously form on a single mother, all of these daughters must be removed to induce reduplication. Intriguingly, the number of daughter centrioles that form during reduplication does not always match the number of ablated daughter centrioles. We also find that exaggeration of the pericentriolar material (PCM) via overexpression of the PCM protein pericentrin in S-arrested CHO cells induces formation of numerous daughter centrioles. We propose that that the size of the PCM cloud associated with the mother centriole restricts the number of daughters that can form simultaneously.This work was supported by grants from the National Institutes of Health (GM GM59363) and the Human Frontiers Science Program (RGP0064). Construction of our laser microsurgery workstation was supported in part by a fellowship from Nikon/Marine Biological Laboratory (A.K.)
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