Is there a minimum complexity required for the biomechanical modelling of running?

Mathematical models have the potential to provide insight into human running. Existing models can be categorised as either simple or complex, and there appears to be a lack of natural progression in model development. By sequentially adding complexity, there is the potential to determine how different mechanical components contribute to the biomechanics of running. In this study, a series of four models, of increasing complexity were developed in OpenSim: a simple spring-mass model, a two-segment model with a torsional spring at the knee and two three-segment models, one with a sprung knee and ankle and another with a sprung knee and actuated ankle. For each model, a forward simulation was developed and model predictions compared with experimental data from 10 forefoot runners. The results showed the spring-mass model overestimated the vertical displacement of the centre of mass (percentage difference: 43.6(22.4)-67.7(21.7)%) and underestimated the vertical ground reaction force (percentage difference: 13.7(8.9)-34.4(10.9)%) compared to the experimental data. Adding a spring at the knee increased the match with the vertical centre of mass displacement (percentage difference: 4.4(25.2)-18.4(40.2)%), however, geometry restrictions meant it was only possible to model approximately 60% of stance. The passive three-segment model showed a good match with centre of mass movements across most of stance (percentage difference in the vertical centre of mass displacement: 4.3(24.5)-21.3(19.2)%), however, actuation at the ankle was required to obtain a closer match with experimental kinetics and joint trajectories (e.g. vertical ground reaction force RMSD decreased by approximately 0.4BW). This is the first study to investigate models of increasing complexity of distance running. The results show that agreement between experimental data and model simulations improves as complexity increases and this provides useful insight into the mechanics of human running

Sex differences in mathematics and reading achievement are inversely related: within- and across-nation assessment of 10 years of PISA data

We analyzed one decade of data collected by the Programme for International Student Assessment (PISA), including the mathematics and reading performance of nearly 1.5 million 15 year olds in 75 countries. Across nations, boys scored higher than girls in mathematics, but lower than girls in reading. The sex difference in reading was three times as large as in mathematics. There was considerable variation in the extent of the sex differences between nations. There are countries without a sex difference in mathematics performance, and in some countries girls scored higher than boys. Boys scored lower in reading in all nations in all four PISA assessments (2000, 2003, 2006, 2009). Contrary to several previous studies, we found no evidence that the sex differences were related to nations’ gender equality indicators. Further, paradoxically, sex differences in mathematics were consistently and strongly inversely correlated with sex differences in reading: Countries with a smaller sex difference in mathematics had a larger sex difference in reading and vice versa. We demonstrate that this was not merely a between-nation, but also a within-nation effect. This effect is related to relative changes in these sex differences across the performance continuum: We did not find a sex difference in mathematics among the lowest performing students, but this is where the sex difference in reading was largest. In contrast, the sex difference in mathematics was largest among the higher performing students, and this is where the sex difference in reading was smallest. The implication is that if policy makers decide that changes in these sex differences are desired, different approaches will be needed to achieve this for reading and mathematics. Interventions that focus on high-achieving girls in mathematics and on low achieving boys in reading are likely to yield the strongest educational benefits

Scalar-field Pressure in Induced Gravity with Higgs Potential and Dark Matter

A model of induced gravity with a Higgs potential is investigated in detail in view of the pressure components related to the scalar-field excitations. The physical consequences emerging as an artifact due to the presence of these pressure terms are analysed in terms of the constraints parting from energy density, solar-relativistic effects and galactic dynamics along with the dark matter halos.Comment: 26 pages, 3 figures, Minor revision, Published in JHE

Static load cycle testing of a low-aspect-ratio four-inch wall, TRG-type structure, TRG-5-4 (1. 0, 0. 56)

This report is the second in a series of test reports that details the quasi-static cyclic testing of low height-to-length aspect ratio reinforced concrete structures. The test structures were designed according to the recommendations of a technical review group for the US Nuclear Regulatory Commission sponsored Seismic Category I Structures Program. The structure tested and reported here had 4-in.-thick shear and end walls, and the elastic deformation was dominated by shear. The background of the program and previous results are given for completeness. Details of the geometry, material property tests, construction history, ultrasonic testing, and modal testing to find the undamaged dynamic characteristics of the structures are given. Next, the static test procedure and results in terms of stiffness and load deformation behavior are given. Finally, results are shown relative to other known results, and conclusions are presented. 33 refs., 140 figs., 13 tabs

Reduction in Phencyclidine Induced Sensorimotor Gating Deficits in the Rat Following Increased System Xc − Activity in the Medial Prefrontal Cortex

Rationale: Aspects of schizophrenia, including deficits in sensorimotor gating, have been linked to glutamate dysfunction and/or oxidative stress in the prefrontal cortex. System xc −, a cystine–glutamate antiporter, is a poorly understood mechanism that contributes to both cellular antioxidant capacity and glutamate homeostasis. Objectives: Our goal was to determine whether increased system xc − activity within the prefrontal cortex would normalize a rodent measure of sensorimotor gating. Methods: In situ hybridization was used to map messenger RNA (mRNA) expression of xCT, the active subunit of system xc −, in the prefrontal cortex. Prepulse inhibition was used to measure sensorimotor gating; deficits in prepulse inhibition were produced using phencyclidine (0.3–3 mg/kg, sc). N-Acetylcysteine (10–100 μM) and the system xc − inhibitor (S)-4-carboxyphenylglycine (CPG, 0.5 μM) were used to increase and decrease system xc − activity, respectively. The uptake of 14C-cystine into tissue punches obtained from the prefrontal cortex was used to assay system xc − activity. Results: The expression of xCT mRNA in the prefrontal cortex was most prominent in a lateral band spanning primarily the prelimbic cortex. Although phencyclidine did not alter the uptake of 14C-cystine in prefrontal cortical tissue punches, intraprefrontal cortical infusion of N-acetylcysteine (10–100 μM) significantly reduced phencyclidine- (1.5 mg/kg, sc) induced deficits in prepulse inhibition. N-Acetylcysteine was without effect when coinfused with CPG (0.5 μM), indicating an involvement of system xc −. Conclusions: These results indicate that phencyclidine disrupts sensorimotor gating through system xc − independent mechanisms, but that increasing cystine–glutamate exchange in the prefrontal cortex is sufficient to reduce behavioral deficits produced by phencyclidine

Curves over every global field violating the local-global principle

There is an algorithm that takes as input a global field k and produces a curve over k violating the local-global principle. Also, given a global field k and a nonnegative integer n, one can effectively construct a curve X over k such that #X(k)=n and X has points over every completion of k.Comment: 5 page

The multiple facets of the Hsp90 machine

International audienceThe Ninth International Conference on the Hsp90 Chaperone Machine concluded in October 2018, in Leysin, Switzerland. The program highlighted findings in various areas, including integrated insight into molecular mechanism of Hsp90, cochaperones, and clients’ structure and function.Heat shock protein-90 (Hsp90) is a molecular chaperone critical for the folding, stability, and activity of client proteins 1. Hsp90 and its orthologs, including bacterial HtpG, mitochondrial TRAP1 and endoplasmic reticulum Grp94, exist as dimers, hydrolyze ATP, and cycle between distinct conformational states. Hsp90 preferentially binds proteins in near native states facilitating their remodeling for protein interactions and signaling. At the 9th International Conference on the Hsp90 Chaperone Machine approximately one-third of the attendees shared their data on Hsp90 structure and function through short talks (Figure 1). Here, we distill and summarize their finding

Three phylogenetic groups have driven the recent population expansion of Cryptococcus neoformans.

Cryptococcus neoformans (C. neoformans var. grubii) is an environmentally acquired pathogen causing 181,000 HIV-associated deaths each year. We sequenced 699 isolates, primarily C. neoformans from HIV-infected patients, from 5 countries in Asia and Africa. The phylogeny of C. neoformans reveals a recent exponential population expansion, consistent with the increase in the number of susceptible hosts. In our study population, this expansion has been driven by three sub-clades of the C. neoformans VNIa lineage; VNIa-4, VNIa-5 and VNIa-93. These three sub-clades account for 91% of clinical isolates sequenced in our study. Combining the genome data with clinical information, we find that the VNIa-93 sub-clade, the most common sub-clade in Uganda and Malawi, was associated with better outcomes than VNIa-4 and VNIa-5, which predominate in Southeast Asia. This study lays the foundation for further work investigating the dominance of VNIa-4, VNIa-5 and VNIa-93 and the association between lineage and clinical phenotype