Still air resistance during walking and running.

In everyday life during terrestrial locomotion our body interacts with two media opposing the forward movement of the body: the ground and the air. Whereas the work done to overcome the ground reaction force has been extensively studied, the work done to overcome still air resistance has been only indirectly estimated by means of theoretical studies and by measurements of the force exerted on puppets simulating the geometry of the human body. In this study, we directly measured the force exerted by still air resistance on eight male subjects during walking and running on an instrumented treadmill with a belt moving at the same speed of a flow of laminar air facing the subject.

The phase shift between potential and kinetic energy in human walking.

It is known that mechanical work to sustain walking is reduced, owing to a transfer of gravitational potential energy into kinetic energy, as in a pendulum. The factors affecting this transfer are unclear. In particular, the phase relationship between potential and kinetic energy curves of the center of mass is not known.

The invasive microalga Chrysophaeum taylorii: Interactive stressors regulate cell density and mucilage production.

The benthic mucilage producing microalga Chrysophaeum taylorii Lewis and Bryan (Pelagophyceae) has recently received attention for its rapid spread in the Mediterranean Sea, where its blooms have remarkable detrimental effects. So far no information on C. taylorii response to multiple stressors, especially in terms of mucilage hyperproduction, is available in the literature yet, and a manipulative field experiment in this topic was designed in Tavolara Punta Coda Cavallo Marine Protected Area.

Running, hopping and trotting: tuning step frequency to the resonant frequency of the bouncing system favors larger animals.

A long-lasting challenge in comparative physiology is to understand why the efficiency of the mechanical work done to maintain locomotion increases with body mass. It has been suggested that this is due to a more elastic step in larger animals. Here, we show in running, hopping and trotting animals, and in human running during growth, that the resonant frequency of the bouncing system decreases with increasing body mass and is, surprisingly, independent of species or gait.

Running humans attain optimal elastic bounce in their teens.

In an ideal elastic bounce of the body, the time during which mechanical energy is released during the push equals the time during which mechanical energy is absorbed during the brake, and the maximal upward velocity attained by the center of mass equals the maximal downward velocity. Deviations from this ideal model, prolonged push duration and lower upward velocity, have found to be greater in older than in younger adult humans. However it is not known how similarity to the elastic bounce changes during growth and whether an optimal elastic bounce is attained at some age.

An analysis of the rebound of the body in backward human running.

Step frequency and energy expenditure are greater in backward running than in forward running. The differences in the motion of the centre of mass of the body associated with these findings are not known. These differences were measured here on nine trained subjects during backward and forward running steps on a force platform at 3-17 km h(-1).

Running backwards: soft landing-hard takeoff, a less efficient rebound.

Human running at low and intermediate speeds is characterized by a greater average force exerted after 'landing', when muscle-tendon units are stretched ('hard landing'), and a lower average force exerted before 'takeoff', when muscle-tendon units shorten ('soft takeoff'). This landing-takeoff asymmetry is consistent with the force-velocity relation of the 'motor' (i.e.

Biomechanics of locomotion in Asian elephants.

Elephants are the biggest living terrestrial animal, weighing up to five tons and measuring up to three metres at the withers. These exceptional dimensions provide certain advantages (e.g.

The bounce of the body in hopping, running and trotting: different machines with the same motor.

The bouncing mechanism of human running is characterized by a shorter duration of the brake after 'landing' compared with a longer duration of the push before 'takeoff'. This landing-takeoff asymmetry has been thought to be a consequence of the force-velocity relation of the muscle, resulting in a greater force exerted during stretching after landing and a lower force developed during shortening before takeoff. However, the asymmetric lever system of the human foot during stance may also be the cause.

The two asymmetries of the bouncing step.

The increase of the push on the ground with increasing running speed improves the "elastic" rebound of the body by privileging the role of tendons relative to muscle within muscle-tendon units.

The landing-take-off asymmetry of human running is enhanced in old age.

The landing-take-off asymmetry of running was thought to derive from, or at least to be consistent with, the physiological property of muscle to resist stretching (after landing) with a force greater than it can develop during shortening (before take-off). In old age, muscular force is reduced, but the deficit in force is less during stretching than during shortening. The greater loss in concentric versus eccentric strength with aging led us to hypothesize that older versus younger adults would increase the landing-take-off asymmetry in running.

Old men running: mechanical work and elastic bounce.

It is known that muscular force is reduced in old age. We investigate what are the effects of this phenomenon on the mechanics of running. We hypothesized that the deficit in force would result in a lower push, causing reduced amplitude of the vertical oscillation, with smaller elastic energy storage and increased step frequency.

The landing-take-off asymmetry in human running.

In the elastic-like bounce of the body at each running step the muscle-tendon units are stretched after landing and recoil before take-off. For convenience, both the velocity of the centre of mass of the body at landing and take-off, and the characteristics of the muscle-tendon units during stretching and recoil, are usually assumed to be the same. The deviation from this symmetrical model has been determined here by measuring the mechanical energy changes of the centre of mass of the body within the running step using a force platform.

Effect of an increase in gravity on the power output and the rebound of the body in human running.

The effect of an increase in gravity on the mechanics of running has been studied by using a force platform fixed to the floor of an aircraft undergoing flight profiles, resulting in a simulated gravity of 1.3 g. The power spent to maintain the motion of the centre of mass of the body is approximately 1.

Pendular energy transduction within the step in human walking.

During walking, the centre of mass of the body moves like that of a 'square wheel': with each step cycle, some of its kinetic energy, E(k), is converted into gravitational potential energy, E(p), and then back into kinetic energy. To move the centre of mass, the locomotory muscles must supply only the power required to overcome the losses occurring during this energy transduction. African women carry loads of up to 20% of their body weight on the head without increasing their energy expenditure.

Energy transfer during stress relaxation of contracting frog muscle fibres.

1. A contracting muscle resists stretching with a force greater than the force it can exert at a constant length, T(o). If the muscle is kept active at the stretched length, the excess tension disappears, at first rapidly and then more slowly (stress relaxation).

Mechanical power and efficiency in running children.

The effect of age and body size on the total mechanical power output (Wtot) during running was studied in children of 3-12 years of age and in adults. Wtot was measured as the sum of the power required to move the body's centre-of-mass relative to the surroundings (the "external power", Wext) plus the power required to move the limbs relative to the body's centre-of-mass (the "internal power", Wint). At low and intermediate speeds (less than about 13 km h-1) the higher step frequency used by young children resulted in a decrease of up to 40-50% in the mass-specific external power and an equal increase in the mass-specific internal power relative to adults.

The role of gravity in human walking: pendular energy exchange, external work and optimal speed.

During walking on Earth, at 1.0 g of gravity, the work done by the muscles to maintain the motion of the centre of mass of the body (W(ext)) is reduced by a pendulum-like exchange between gravitational potential energy and kinetic energy. The weight-specific W(ext) per unit distance attains a minimum of 0.

Effect of stretching on undamped elasticity in muscle fibres from Rana temporaria.

Muscle stiffness was measured from the undamped elastic recoil taking place when the force attained during ramp stretches of muscle fibres, tetanized on the plateau of the tension-length relation, was suddenly reduced to the isometric value developed before the stretch, T0. Sarcomere elastic recoil was measured on a tendon-free segment of the fibre by means of a striation follower. After small ramp stretches, stiffness increases to a value 1.

Muscle work enhancement by stretch. Passive visco-elasticity or cross-bridges?

Tetanized frog muscle fibres subjected to ramp stretches on the plateau of the tension-length relation, followed by an isotonic release against a load equal to the maximum isometric tension (T0), exhibit a well defined transient shortening against T0 which was attributed to the release of mechanical energy stored during stretching within the damped element of the cross-bridges. However, this interpretation has recently been challenged, and 'transient shortening against T0' has instead been attributed to elastic elements strained because of non-uniform distribution of lengthening within the fibre volume. The 'excess length change', resulting from the recoil of these elastic elements, was found i) to increase continuously with stretch amplitude up to 50 nm per h.

The mechanics of running in children.

1. The effect of age and body size on the bouncing mechanism of running was studied in children aged 2-16 years. 2.

The resonant step frequency in human running.

At running speeds less than about 13 km h-1 the freely chosen step frequency (ffree) is lower than the frequency at which the mechanical power is minimized (fmin). This dissociation between ffree and fmin was investigated by measuring mechanical power, metabolic energy expenditure and apparent natural frequency of the body's bouncing system (fsist) during running at three given speeds with different step frequencies. The ffree requires a mechanical power greater than that at fmin mainly due to a larger vertical oscillation of the body at each step.