179 research outputs found

    The effect of temporally variable environmental stimuli and group size on emergence behavior

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    How animals trade-off food availability and predation threats is a strong determinant of animal activity and behavior; however, the majority of work on this topic has been on individual animals, despite the modulating effect the presence of conspecifics can have on both foraging and predation risk. Although these environmental factors (food and predation threat) vary spatially within habitats, they also vary temporally, and in marine habitats, this can be determined by not only the diel cycle but also the tidal cycle. Humbug damselfish, Dascyllus aruanus, live in small groups of unrelated individuals within and around branching coral heads, which they collectively withdraw into to escape a predation threat. In this study, we measured the proportion of individuals in the colony that were outside the coral head before and after they were scared by a fright stimulus and compared the responses at high tide (HT) and low tide (LT). We found that a greater proportion of the shoal emerged after the fright stimulus at HT and in larger groups than at LT or in smaller groups. We also quantified the pattern of emergence over time and discovered the rate of emergence was faster in larger shoals as time progressed. We show that shoals of fish change their behavioral response to a predation threat in accordance with the tide, exemplifying how temporally variable environmental factors can shape group movement decisions

    MICC: A tool for computing short distances in the curve complex

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    The complex of curves C(Sg)\mathcal{C}(S_g) of a closed orientable surface of genus g≥2g \geq 2 is the simplicial complex having its vertices, C0(Sg)\mathcal{C}^0(S_g), are isotopy classes of essential curves in SgS_g. Two vertices co-bound an edge of the 11-skeleton, C1(Sg)\mathcal{C}^1(S_g), if there are disjoint representatives in SgS_g. A metric is obtained on C0(Sg)\mathcal{C}^0(S_g) by assigning unit length to each edge of C1(Sg)\mathcal{C}^1(S_g). Thus, the distance between two vertices, d(v,w)d(v,w), corresponds to the length of a geodesic---a shortest edge-path between vv and ww in C1(Sg)\mathcal{C}^1 (S_g). Recently, Birman, Margalit and the second author introduced the concept of {\em initially efficient geodesics} in C1(Sg)\mathcal{C}^1(S_g) and used them to give a new algorithm for computing the distance between vertices. In this note we introduce the software package MICC ({\em Metric in the Curve Complex}), a partial implementation of the initially efficient geodesic algorithm. We discuss the mathematics underlying MICC and give applications. In particular, we give examples of distance four vertex pairs, for g=2g=2 and 3. Previously, there was only one known example, in genus 22, due to John Hempel.Comment: 19 pages, 9 figures, Version 2 has updated figures and reference

    High-temperature ceramic coatings used in aero engine environments

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    This paper reviews the role of ceramic coatings technology in the hot sections of modern gas turbine engines by contrasting the role of surface engineering and coatings away from secondary reliance (i.e. the coating extending the life of the component and when the coating is lost or fails there is still an appreciable remnant life of the component) to prime reliance where the failure of the coating would result in a rapid failure of the component. To illustrate this change in design philosophy, the coating systems deployed in the HP turbine module in both shrouded and unshrouded configurations are discussed by comparing the performance of first and second generation coating systems

    Elliptic Reciprocity

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    The paper introduces the notions of an elliptic pair, an elliptic cycle and an elliptic list over a square free positive integer d. These concepts are related to the notions of amicable pairs of primes and aliquot cycles that were introduced by Silverman and Stange. Settling a matter left open by Silverman and Stange it is shown that for d=3 there are elliptic cycles of length 6. For d not equal to 3 the question of the existence of proper elliptic lists of length n over d is reduced to the the theory of prime producing quadratic polynomials. For d=163 a proper elliptic list of length 40 is exhibited. It is shown that for each d there is an upper bound on the length of a proper elliptic list over d. The final section of the paper contains heuristic arguments supporting conjectured asymptotics for the number of elliptic pairs below integer X. Finally, for d congruent to 3 modulo 8 the existence of infinitely many anomalous prime numbers is derived from Bunyakowski's Conjecture for quadratic polynomials.Comment: 17 pages, including one figure and two table

    Analytical Study of KOH Wet Etch Surface Passivation for III-Nitride Micropillars

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    III-Nitride micropillar structures show great promise for applications in micro light-emitting diodes and vertical power transistors due to their excellent scalability and outstanding electrical properties. Typically, III-Nitride micropillars are fabricated through a top-down approach using reactive ion etch which leads to roughened, non-vertical sidewalls that results in significant performance degradation. Thus, it is essential to remove this plasma etch induced surface damage. Here, we show that potassium hydroxide (KOH) acts as a crystallographic etchant for III-Nitride micropillars, preferentially exposing the vertical m-plane, and effectively removing dry etch damage and reducing the structure diameter at up to 36.6 nm/min. Both KOH solution temperature and concentration have a dramatic effect on this wet etch progression. We found that a solution of 20% AZ400K (2% KOH) at 90 C is effective at producing smooth, highly vertical sidewalls with RMS surface roughness as low as 2.59 nm, ideal for high-performance electronic and optoelectronic devices.Comment: 7 pages, 7 figure

    Delivering an In-Home Exercise Program via Telerehabilitation: A Pilot Study of Lung Transplant Go (LTGO)

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    We evaluated the feasibility, safety, system usability, and intervention acceptability of Lung Transplant Go (LTGO), an 8-week in-home exercise intervention for lung transplant recipients using a telerehabilitation platform, and described changes in physical function and physical activity from baseline to post-intervention. The intervention was delivered to lung transplant recipients in their home via the Versatile and Integrated System for TeleRehabilitation (VISYTER). The intervention focused on aerobic and strengthening exercises tailored to baseline physical function. Participants improved walk distance (6-minute walk distance), balance (Berg Balance Scale), lower body strength (30-second chair stand test) and steps walked (SenseWear Armband®). No adverse events were reported. Participants rated the program highly positively in regard to the technology and intervention. The telerehabilitation exercise program was feasible, safe, and acceptable. Our findings provide preliminary support for the LTGO intervention to improve physical function and promote physical activity in lung transplant recipients.

    MicroRNA-143 activation regulates smooth muscle and endothelial cell crosstalk in pulmonary arterial hypertension

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    Rationale: The pathogenesis of PAH remains unclear. The four microRNAs representing the miR-143 and miR-145 stem loops are genomically clustered. Objective: To elucidate the transcriptional regulation of the miR-143/145 cluster, and the role of miR-143 in PAH. Methods and Results: We identified the promoter region that regulates miR-143/145 miRNA expression in pulmonary artery smooth muscle cells (PASMCs). We mapped PAH-related signalling pathways, including estrogens receptor (ER), liver X factor/retinoic X receptor (LXR/RXR), TGF-β (Smads), and hypoxia (HRE) that regulated levels of all pri-miR stem loop transcription and resulting miRNA expression. We observed that miR-143-3p is selectively upregulated compared to miR-143-5p during PASMC migration. Modulation of miR-143 in PASMCs significantly altered cell migration and apoptosis. In addition, we found high abundance of miR-143-3p in PASMCs-derived exosomes. Using assays with pulmonary arterial endothelial cells (PAECs) we demonstrated a paracrine pro-migratory and pro-angiogenic effect of miR-143-3p enriched exosomes from PASMC. Quantitative PCR and in situ hybridisation showed elevated expression of miR-143 in calf models of PAH as well as in samples from PAH patients. Moreover, in contrast to our previous findings that had not supported a therapeutic role in vivo, we now demonstrate a protective role for miR-143 in experimental PH in vivo in miR-143-/- and antimiR143-3p-treated mice exposed to chronic hypoxia in both preventative and reversal settings. Conclusions: MiR-143-3p modulated both cellular and exosome-mediated responses in pulmonary vascular cells, while inhibition of miR-143-3p blocked experimental PH. Taken together these findings confirm an important role for the miR-143/145 cluster in PAH pathobiology

    Myocardin regulates vascular smooth muscle cell inflammatory activation and disease.

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    OBJECTIVE: Atherosclerosis, the cause of 50% of deaths in westernized societies, is widely regarded as a chronic vascular inflammatory disease. Vascular smooth muscle cell (VSMC) inflammatory activation in response to local proinflammatory stimuli contributes to disease progression and is a pervasive feature in developing atherosclerotic plaques. Therefore, it is of considerable therapeutic importance to identify mechanisms that regulate the VSMC inflammatory response. APPROACH AND RESULTS: We report that myocardin, a powerful myogenic transcriptional coactivator, negatively regulates VSMC inflammatory activation and vascular disease. Myocardin levels are reduced during atherosclerosis, in association with phenotypic switching of smooth muscle cells. Myocardin deficiency accelerates atherogenesis in hypercholesterolemic apolipoprotein E(-/-) mice. Conversely, increased myocardin expression potently abrogates the induction of an array of inflammatory cytokines, chemokines, and adhesion molecules in VSMCs. Expression of myocardin in VSMCs reduces lipid uptake, macrophage interaction, chemotaxis, and macrophage-endothelial tethering in vitro, and attenuates monocyte accumulation within developing lesions in vivo. These results demonstrate that endogenous levels of myocardin are a critical regulator of vessel inflammation. CONCLUSIONS: We propose myocardin as a guardian of the contractile, noninflammatory VSMC phenotype, with loss of myocardin representing a critical permissive step in the process of phenotypic transition and inflammatory activation, at the onset of vascular disease.This work was supported by Wellcome Trust funding for MAJ (Studentship 086799/Z/08/Z), British Heart Foundation grants (PG/10/007/28184) for AT, and (RG/08/009/25841) for MRB, and SS (FS/13/29/30024), the Cambridge NIHR Biomedical Research Centre and the NIH for JM (NIH HL-117907).This is the accepted manuscript of a paper published in Arteriosclerosis, Thrombosis, and Vascular Biology, 2015, doi: 10.1161/ATVBAHA.114.30521

    Investigation of 1P-LSD as a Novel Drug Therapy for Autism Spectrum Disorders

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    Autism spectrum disorders (ASD), defined by repetitive behaviors or impaired social communication, is a prevalent yet relatively misunderstood set of conditions. ASD encompasses a series of neurodevelopmental disorders that have various physiological manifestations (Goines & Ashwood, 2013). Due to the heterogeneity of ASD, the true mechanisms leading to the development of ASD and its symptoms remain unclear and require more research (Rossignol & Frye, 2012; Watts, 2008). The purpose of this project is to test whether or not 1P-LSD, an analogue of LSD (lysergic acid diethylamide), has the potential to treat symptoms of ASD, specifically the hyperexcitation of N-methyl-D-aspartate (NMDA) receptors in the brain which causes the neuronal excitotoxicity highly implicated in the pathology of ASD.We will determine the two highest doses of 1P-LSD which does not result in any hallucinogenic side effects in Phase 1 of this protocol and utilize these doses towards treatment of symptoms associated with ASD in the Phase 2 of this protocol. We will monitor N-methyl-D-aspartate (NMDA) receptor activity, which is usually impaired in ASD, following microdosing of 1P-LSD. Towards these experiments, we will be using an autistic mouse model, Slc6a4, compared to normal mice (C57BL/6J). The efficacy of the treatment model will be assessed by measuring the levels of a subunit of the NMDA receptor, the NR2B subunit, using with western blotting and immunohistochemistry, and by measuring the levels of glutamate using gas chromatography-mass spectrometry (GCMS).Launch UMD donor
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