14,527 research outputs found

    The impact of stress on financial decision-making varies as a function of depression and anxiety symptoms.

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    Stress can precipitate the onset of mood and anxiety disorders. This may occur, at least in part, via a modulatory effect of stress on decision-making. Some individuals are, however, more resilient to the effects of stress than others. The mechanisms underlying such vulnerability differences are nevertheless unknown. In this study we attempted to begin quantifying individual differences in vulnerability by exploring the effect of experimentally induced stress on decision-making. The threat of unpredictable shock was used to induce stress in healthy volunteers (N = 47) using a within-subjects, within-session design, and its impact on a financial decision-making task (the Iowa Gambling Task) was assessed alongside anxious and depressive symptomatology. As expected, participants learned to select advantageous decks and avoid disadvantageous decks. Importantly, we found that stress provoked a pattern of harm-avoidant behaviour (decreased selection of disadvantageous decks) in individuals with low levels of trait anxiety. By contrast, individuals with high trait anxiety demonstrated the opposite pattern: stress-induced risk-seeking (increased selection of disadvantageous decks). These contrasting influences of stress depending on mood and anxiety symptoms might provide insight into vulnerability to common mental illness. In particular, we speculate that those who adopt a more harm-avoidant strategy may be better able to regulate their exposure to further environmental stress, reducing their susceptibility to mood and anxiety disorders

    Non-dispersive and weakly dispersive single-layer flow over an axisymmetric obstacle: the equivalent aerofoil formulation

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    Non-dispersive and weakly dispersive single-layer flows over axisymmetric obstacles, of non-dimensional height M measured relative to the layer depth, are investigated. The case of transcritical flow, for which the Froude number F of the oncoming flow is close to unity, and that of supercritical flow, for which F > 1, are considered. For transcritical flow, a similarity theory is developed for small obstacle height and, for non-dispersive flow, the problem is shown to be isomorphic to that of the transonic flow of a compressible gas over a thin aerofoil. The non-dimensional drag exerted by the obstacle on the flow takes the form D(Gamma)M-5/3, where Gamma = (F - 1)M-2/3 is a transcritical similarity parameter and D is a function which depends on the shape of the 'equivalent aerofoil' specific to the obstacle. The theory is verified numerically by comparing results from a shock-capturing shallow-water model with corresponding solutions of the transonic small-disturbance equation, and is found to be generally accurate for M less than or similar to 0.4 and vertical bar Gamma vertical bar less than or similar to 1. In weakly dispersive flow the equivalent aerofoil becomes the boundary condition for the Kadomtsev-Petviashvili equation and (multiple) solitary waves replace hydraulic jumps in the resulting flow patterns.For Gamma greater than or similar to 1.5 the transcritical similarity theory is found to be inaccurate and, for small M, flow patterns are well described by a supercritical theory, in which the flow is determined by the linear solution near the obstacle. In this regime the drag is shown to be c(d)M(2)/(F root F-2 - 1), where c(d) is a constant dependent on the obstacle shape. Away from the obstacle, in non-dispersive flow the far-field behaviour is known to be described by the N-wave theory of Whitham and in dispersive flow by the Kortewegde Vries equation. In the latter case the number of emergent solitary waves in the wake is shown to be a function of A = 3M/(2 delta(2) root F-2 - 1), where delta is the ratio of the undisturbed layer depth to the radial scale of the obstacle

    Cell type-specific profiling of protein-DNA interactions without cell isolation using Targeted DamID with next-generation sequencing

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    The ability to profile transcription and chromatin binding in a cell type-specific manner is a powerful approach for understanding cell fate specification and cellular function in multicellular organisms. We recently developed Targeted DamID (TaDa) to enable genome-wide, cell-type-specific profiling of DNA- and chromatin-binding proteins in vivo without cell isolation. As a Protocol Extension, this article describes substantial modifications to an existing Protocol and offers additional applications. TaDa builds upon DamID, a technique for detecting genome-wide DNA binding profiles of proteins, by coupling it with the GAL4 system in Drosophila to enable both temporal and spatial resolution. TaDa ensures that Dam-fusion proteins are expressed at very low levels, avoiding toxicity and potential artefacts from over-expression. The modifications to the core DamID technique presented here also increase the speed of sample processing and throughput, and adapt the method to Nextgeneration Sequencing technology. TaDa is robust, reproducible, and highly sensitive. Compared to other methods for cell-type specific profiling, the technique requires no cell-sorting, crosslinking or antisera, and binding profiles can be generated from as few as 10,000 total induced cells. By profiling the genome-wide binding of RNA polymerase II, TaDa can also identify transcribed genes in a cell type-specific manner. Here we describe a detailed protocol for carrying out TaDa experiments and preparing the material for next generation sequencing. Although we developed TaDa in Drosophila, it should be easily adapted to other organisms with an inducible expression system. Once transgenic animals are obtained, the entire experimental procedure – from collecting tissue samples to generating sequencing libraries – can be accomplished within 5 days

    Transcritical rotating flow over topography

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    The flow of a one-and-a-half layer fluid over a three-dimensional obstacle of non-dimensional height M, relative to the lower layer depth, is investigated in the presence of rotation, the magnitude of which is measured by a non-dimensional parameter B (inverse Burger number). The transcritical regime in which the Froude number F, the ratio of the flow speed to the interfacial gravity wave speed, is close to unity is considered in the shallow-water (small-aspect-ratio) limit. For weakly rotating flow over a small isolated obstacle (M -> 0) a similarity theory is developed in which the behaviour is shown to depend on the parameters Gamma = (F - 1)M-2/3 and nu = (BM-1/3)-M-1/2. The flow pattern in this regime is determined by a nonlinear equation in which Gamma and nu appear explicitly, termed here the 'rotating transcritical small-disturbance equation' (rTSD equation, following the analogy with compressible gasdynamics). The rTSD equation is forced by 'equivalent aerofoil' boundary conditions specific to each obstacle. Several qualitatively new flow behaviours are exhibited, and the parameter reduction afforded by the theory allows a (Gamma, nu) regime diagram describing these behaviours to be constructed numerically. One important result is that, in a supercritical oncoming flow in the presence of sufficient rotation (nu greater than or similar to 2), hydraulic jumps can appear downstream of the obstacle even in the absence of an upstream jump. Rotation is found to have the general effect of increasing the amplitude of any existing downstream hydraulic jumps and reducing the lateral extent and amplitude of upstream jumps. Numerical results are compared with results from a shock-capturing shallow-water model, and the (Gamma, nu) regime diagram is found to give good qualitative and quantitative predictions of flow patterns at finite obstacle height (at least for M less than or similar to 0.4). Results are compared and contrasted with those for a two-dimensional obstacle or ridge, for which rotation also causes hydraulic jumps to form downstream of the obstacle and acts to attenuate upstream jumps

    Seiberg-Witten prepotential for E-string theory and random partitions

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    We find a Nekrasov-type expression for the Seiberg-Witten prepotential for the six-dimensional non-critical E_8 string theory toroidally compactified down to four dimensions. The prepotential represents the BPS partition function of the E_8 strings wound around one of the circles of the toroidal compactification with general winding numbers and momenta. We show that our expression exhibits expected modular properties. In particular, we prove that it obeys the modular anomaly equation known to be satisfied by the prepotential.Comment: 14 page

    Shoot and plantlet regeneration from meristems of Dioscorea rotundata Poir and Dioscorea alata L.

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    In vitro culture media capable of regenerating moderate to high shoots and/or plantlets from meristems of two yam species - Dioscorea rotundata and Dioscorea alata within comparable duration of 10 weeks as commonly obtained in other monocots and root and tuber crops were investigated. The study comprised 125 phytohormone combinations investigated in three factorial experiments each consisting of an auxin (NAA) and a cytokinin (BAP or kinetin), or two cytokinins only. The frequency of direct plantlet regeneration, though significantly (P < 0.05) higher for D. alata than for D. rotundata, was low and ranged from 0 to 10% at 3 weeks after culture (WAC) and 0 to 35% at 8 WAC. At 8 WAC, shoot regeneration of 42-75% was obtained in D. rotundata in MS medium supplemented with 0.1 M NAA + 0.20 M BAP, and shoot + plantlet regeneration of 60-82% obtained in media containing 0.05 M + 0.20 M BAP or 0.46 M BAP + 0.50 M kinetin in D. alata. Both shoot induction and plantlet regeneration were species-dependent. Induced shoots were successfully rooted in MS medium within 3 to 4 weeks, bringing time taken for plantlet regeneration to 11 to 12 weeks. Regenerants were morphologically similar to the mother plants. Results of the present study will facilitate regeneration of plantlets via meristem in D. rotundata and D. alata

    Web-based Gene Pathogenicity Analysis (WGPA): a web platform to interpret gene pathogenicity from personal genome data

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    UNLABELLED: As the volume of patient-specific genome sequences increases the focus of biomedical research is switching from the detection of disease-mutations to their interpretation. To this end a number of techniques have been developed that use mutation data collected within a population to predict whether individual genes are likely to be disease-causing or not. As both sequence data and associated analysis tools proliferate, it becomes increasingly difficult for the community to make sense of these data and their implications. Moreover, no single analysis tool is likely to capture all relevant genomic features that contribute to the gene's pathogenicity. Here, we introduce Web-based Gene Pathogenicity Analysis (WGPA), a web-based tool to analyze genes impacted by mutations and rank them through the integration of existing prioritization tools, which assess different aspects of gene pathogenicity using population-level sequence data. Additionally, to explore the polygenic contribution of mutations to disease, WGPA implements gene set enrichment analysis to prioritize disease-causing genes and gene interaction networks, therefore providing a comprehensive annotation of personal genomes data in disease. AVAILABILITY AND IMPLEMENTATION: wgpa.systems-genetics.net
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