Both the linear leg spring model and the two-segment leg model with constant spring stiffness have been broadly used as template models to investigate bouncing gaits for legged robots with compliant legs. In addition to these two models, the other stiffness leg spring models developed using inspiration from biological characteristic have the potential to improve high-speed running capacity of s...

Background. There is sparse literature examining the ICB phase of aerobic- and anaerobic-trained athletes. Measurements of ICB phase values of athletes can help to evaluate the sport’s physiological demands and understand the physiological adaptations in response to physical training. Objectives. The purpose of this study was to examine the relationship between the isocapnic buffering (IC...

the present study aimed to examine the effect of contextual interference on acquisition, retention and transfer of coincidence anticipation task with constant, increasing and decreasing speeds. 36 male physical education participants from shahid beheshti university were voluntarily selected and randomly divided into three groups (12 subjects each group) and performed coincidence timing tasks wi...

Cortical and hippocampal gamma oscillations have been implicated in many behavioral tasks. The hippocampus is required for spatial navigation where animals run at varying speeds. Hence we tested the hypothesis that the gamma rhythm could encode the running speed of mice. We found that the amplitude of slow (20-45 Hz) and fast (45-120 Hz) gamma rhythms in the hippocampal local field potential (L...

A widely held assumption is that metabolic rate (Ė(met)) during legged locomotion is linked to the mechanics of different gaits and this linkage helps explain the preferred speeds of animals in nature. However, despite several prominent exceptions, Ė(met) of walking and running vertebrates has been nearly uniformly characterized as increasing linearly with speed across all gaits. This descripti...

1. Data were compiled from the literature and our own studies on 24 ant species to characterise the effects of body size and temperature on forager running speed. 2. Running speed increases with temperature in a manner consistent with the effects of temperature on metabolic rate and the kinetic properties of muscles. 3. The exponent of the body mass-running speed allometry ranged from 0.14 to 0...

Movement speed is fundamental to all animal behaviour, yet no general framework exists for understanding why animals move at the speeds they do. Even during fitness-defining behaviours like running away from predators, an animal should select a speed that balances the benefits of high speed against the increased probability of mistakes. In this study, we explored this idea by quantifying trade-...

Several lines of evidence indicate that the sarco(endo)plasmic reticulum ATPase type 2 (SERCA2) is essential for maintaining myocardial calcium handling and cardiac pump function. Hence, a reduction in SERCA2 abundance is expected to reduce work performance and maximal oxygen uptake (VO2max) and to limit the response to exercise training. To test this hypothesis, we compared VO2max and exercise...

Uphill running requires more energy than level running at the same speed, largely due to the additional mechanical work of elevating the body weight. We explored the distribution of energy use among the leg muscles of guinea fowl running on the level and uphill using both organismal energy expenditure (oxygen consumption) and muscle blood flow measurements. We tested each bird under four condit...

Notably absent from the existing literature is an explicit biomechanical model linking limb design to the energy cost of locomotion, COL. Here, I present a simple model that predicts the rate of force production necessary to support the body and swing the limb during walking and running as a function of speed, limb length, limb proportion, excursion angle and stride frequency. The estimated rat...