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Rémi Hackert

Publications and source records attributed to Rémi Hackert.

4 recordsLinked to original sources

Experimental study of coordination patterns during unsteady locomotion in mammals.

A framework to study interlimb coordination, which allowed the analysis of all the symmetrical and asymmetrical gaits, was recently proposed. It suggests that gait depends on a common basic pattern controlling the coordination of the forelimbs (fore lag, FL), the coordination of the hindlimbs (hind lag, HL) and the relationship between these two pairs of limbs (pair lag, PL) in an anteroposterior sequence of movement (APS). These three time parameters are sufficient for identifying all steady gaits. We assumed in this work that this same framework could also be used to study non-steady locomotion, particularly the transitions between symmetrical and asymmetrical gaits. Moreover, as the limbs are coordinated in time and also in space during locomotion, we associated three analogous space parameters (fore gap, FG; hind gap, HG and pair gap, PG) to the three time parameters. We studied the interlimb coordination of dogs and cats moving on a runway with a symmetrical gait. In the middle of the runway, the gait was disturbed by an obstacle, and the animal had to change to an asymmetrical coordination to get over it. The time (FL, HL, PL) and space (FG, HG, PG) parameters of each sequence of the trials were calculated. The results demonstrated that the APS method allows quantification of the interlimb coordination during the symmetrical and asymmetrical phases and during the transition between them, in both dogs and cats. The space and time parameters make it possible to link the timing and the spacing of the footfalls, and to quantify the spatiotemporal dimension of gaits in different mammals. The slight differences observed between dogs and cats could reflect their morphological differences. The APS method could thus be used to understand the implication of morphology in interlimb coordination. All these results are consistent with current knowledge in biomechanics and neurobiology, therefore the APS reflects the actual biological functioning of quadrupedal interlimb coordination.

Animals↗

Sagittal spine movements of small therian mammals during asymmetrical gaits.

Mammalian locomotion is characterized by the use of asymmetrical gaits associated with extensive flexions and extensions of the body axis. Although the impact of sagittal spine movements on locomotion is well known, little information is available on the kinematics of spinal motion. Intervertebral joint movements were studied in two metatherian and three eutherian species during the gallop and halfbound using high-speed cineradiography. Fast-Fourier transformation was used to filter out high frequency digitizing errors and keep the lower frequency sinusoid oscillations that characterize the intervertebral angular movements. Independent of their regional classification as thoracic or lumbar vertebrae, 7+/-1 presacral intervertebral joints were involved in sagittal bending movements. In only one species, no more than five intervertebral joints contributed to the resulting 'pelvic movement'. In general, the trunk region involved in sagittal bending during locomotion did not correspond to the traditional subdivisions of the vertebral column (e.g. as thoracic and lumbar or pre- and postdiaphragmatic region). Therefore, these classifications do not predict the regions involved in spinal oscillations during locomotion. Independent of the gait, maximum flexion of the spine was observed in the interval between the last third of the swing phase and touch-down. This results in a retraction of the pelvis and hindlimbs before touch-down and, we hypothesize, enhances the stability of the system. Maximum extension occurred during the first third of the swing phase (i.e. after lift-off) in all species. In general, the observed timing of dorsoventral oscillations of the spine are in accordance with that observed in other mammals and with activity data of respiratory and epaxial back muscles. Although no strict craniocaudal pattern was observable, the more cranial intervertebral joints tend to flex and extend earlier than the more caudal ones. This is in accordance with the organization and the activation of the paravertebral musculature in mammals. The amplitude of intervertebral joint movements increased caudally, reaching its highest values in the presacral joint. The more intense sagittal bending movements in the caudal intervertebral joints are reflected by the muscle fiber type composition of the back muscles involved. Despite the highly similar amplitude of 'pelvic motion', touch-down and lift-off positions of the pelvis were clearly different between the species with a long, external tail and those with no external tail.

Animals↗

Biomimetic robotics should be based on functional morphology.

Due to technological improvements made during the last decade, bipedal robots today present a surprisingly high level of humanoid skill. Autonomy, with respect to the processing of information, is realized to a relatively high degree. What is mainly lacking in robotics, moving from purely anthropomorphic robots to 'anthropofunctional' machines, is energetic autonomy. In a previously published analysis, we showed that closer attention to the functional morphology of human walking could give robotic engineers the experiences of an at least 6 Myr beta test period on minimization of power requirements for biped locomotion. From our point of view, there are two main features that facilitate sustained walking in modern humans. The first main feature is the existence of 'energetically optimal velocities' provided by the systematic use of various resonance mechanisms: (a). suspended pendula (involving arms as well as legs in the swing phase of the gait cycle) and matching of the pendular length of the upper and lower limbs; (b). inverted pendula (involving the legs in the stance phase), driven by torsional springs around the ankle joints; and (c). torsional springs in the trunk. The second main feature is compensation for undesirable torques induced by the inertial properties of the swinging extremities: (a). mass distribution in the trunk characterized by maximized mass moments of inertia; (b). lever arms of joint forces at the hip and shoulder, which are inversely proportional to their amplitude; and (c). twisting of the trunk, especially torsion. Our qualitative conclusions are three-fold. (1). Human walking is an interplay between masses, gravity and elasticity, which is modulated by musculature. Rigid body mechanics is insufficient to describe human walking. Thus anthropomorphic robots completely following the rules of rigid body mechanics cannot be functionally humanoid. (2). Humans are vertebrates. Thus, anthropomorphic robots that do not use the trunk for purposes of motion are not truly humanoid. (3). The occurrence of a waist, especially characteristic of humans, implies the existence of rotations between the upper trunk (head, neck, pectoral girdle and thorax) and the lower trunk (pelvic girdle) via an elastic joint (spine, paravertebral and abdominal musculature). A torsional twist around longitudinal axes seems to be the most important.

Adult↗

Torque patterns of the limbs of small therian mammals during locomotion on flat ground.

In three species of small therian mammals (Scandentia: Tupaia glis, Rodentia: Galea musteloides and Lagomorpha: Ochotona rufescens) the net joint forces and torques acting during stance phase in the four kinematically relevant joints of the forelimbs (scapular pivot, shoulder joint, elbow joint, wrist joint) and the hindlimbs (hip joint, knee joint, ankle joint, intratarsal joint) were determined by inverse dynamic analysis. Kinematics were measured by cineradiography (150 frames s(-1)). Synchronously ground reaction forces were acquired by forceplates. Morphometry of the extremities was performed by a scanning method using structured illumination. The vector sum of ground reaction forces and weight accounts for most of the joint force vector. Inertial effects can be neglected since errors of net joint forces amount at most to 10 %. The general time course of joint torques is comparable for all species in all joints of the forelimb and in the ankle joint. Torques in the intratarsal joints differ between tailed and tail-less species. The torque patterns in the knee and hip joint are unique to each species. For the first time torque patterns are described completely for the forelimb including the scapula as the dominant propulsive segment. The results are compared with the few torque data available for various joints of cats (Felis catus), dogs (Canis lupus f. familiaris), goats (Capra sp.) and horses (Equus przewalskii f. caballus).

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