PubMed Health⌕ Search

Biomedical subjects

Peter Aerts

Publications and source records attributed to Peter Aerts.

33 records · Page 2Linked to original sources

A functional morphological approach to the scaling of the feeding system in the African catfish, Clarias gariepinus.

Effects of size are pervasive and affect nearly all aspects of the biology of animals and plants. Theoretical scaling models have been developed to predict the effects of size on the functioning of musculo-skeletal systems. Although numerous experimental studies have investigated the effects of size on the movements of skeletal elements during locomotion and feeding in vertebrates, relatively little is known about the scaling of the muscles and bones responsible for the actual movements. Here, we examine the scaling of external morphology, skeletal elements of the feeding system, and a number of cranial muscles to understand how this may affect the movements observed during suction feeding in the African catfish, Clarias gariepinus. The results show that neither the head nor the cranial elements themselves scale according to geometric similarity models. Relative to head size, distinct changes in the mass and configuration of the feeding structures takes place. Unexpectedly, different cranial muscles show different scaling patterns that ultimately all lead to a positive allometry of muscle cross-sectional area relative to fish head size. This suggests that (1) the scaling of the cranial elements cannot be predicted a priori based on the scaling of external head dimensions and (2) the scaling of the feeding system is optimised towards high force output in the larger animals. An analysis of the consequences of the observed changes in morphology with size on performance traits, including bite force and jaw closing velocity, suggests a tight link between the scaling of the feeding system and the natural diet of these fish. Whereas for smaller size classes the system is tuned towards high bite forces, for animals with cranial lengths greater than 65 mm the scaling of the feeding system appears to be dictated by the hydrodynamic constraints on suction feeding.

Africa↗

A test of mouth-opening and hyoid-depression mechanisms during prey capture in a catfish using high-speed cineradiography.

Detailed morphological analyses have identified a number of different mechanical pathways by which the morphologically complex cranial system of fishes can achieve mouth opening and hyoid depression. However, many of these proposed mechanisms remain untested. Furthermore, very little is known about the precise timing of activity of each of these mechanisms, and about the magnitude of each mechanism's total contribution to its proposed function. In the present study, all mouth opening and hyoid depression mechanisms described for Clarias gariepinus, an air-breathing catfish, are analysed. High-speed X-ray videos were recorded during prey capture of three catfish implanted with small, radio-opaque markers in the cranial elements potentially involved. A kinematic analysis was performed from which data were used as input in planar four-bar models. This analysis shows that the opercular mouth-opening mechanism initiates mouth opening, but is not able to cause the complete mouth openings as observed on the X-ray videos. The latter is accomplished through the protractor hyoidei muscles, which couple hyoid depression to lower jaw depression in a four-bar system and also reinforce lower jaw depression by shortening during the final stage of mouth opening. Although the angulo-ceratohyal ligament was previously hypothesised to play a part in mouth opening, our results show that it probably does not, but rather functions as a hyoid-elevator during mouth closure. Finally, hyoid depression is exclusively achieved by the four-bar mechanism involving neurocranial elevation and pectoral girdle retraction, generally without any reinforcement by shortening of the sternohyoideus muscle. In contrast to the results from a recent analysis on sunfish, the catfish's sternohyoideus gradually elongates during hyoid depression.

Animals↗

A dynamic model of mouth closing movements in clariid catfishes: the role of enlarged jaw adductors.

Some species of Clariidae (air breathing catfishes) have extremely large (hypertrophied) jaw closure muscles. Besides producing higher bite forces, the enlarged muscles may also cause higher accelerations of the lower jaw during rapid mouth closure. Thus, jaw adductor hypertrophy could potentially also enable faster mouth closure. In this study, a forward dynamic model of jaw closing is developed to evaluate the importance of jaw adductor hypertrophy on the speed of mouth closure. The model includes inertia, pressure, tissue resistance and hydrodynamic drag forces on the lower jaw, which is modelled as a rotating half-ellipse. Simulations are run for four clariid species showing a gradual increase in jaw adductor hypertrophy (Clarias gariepinus, Clariallabes longicauda, Gymnallabes typus and Channallabes apus). The model was validated using data from high-speed videos of prey captures in these species. In general, the kinematic profiles of the fastest mouth closure from each species are reasonably well predicted by the model. The model was also used to compare the four species during standardized mouth closures (same initial gape angle, travel distance and cranial size). These simulations suggest that the species with enlarged jaw adductors have an increased speed of jaw closure (in comparison with the non-hypertrophied C. gariepinus) for short lower jaw rotations and when feeding at high gape angles. Consequently, the jaw system in these species seems well equipped to capture relatively large, evasive prey. For prey captures during which the lower jaw rotates freely over a larger distance before impacting the prey, the higher kinematic efficiency of the C. gariepinus jaw system results in the fastest jaw closures. In all cases, the model predicts that an increase in the physiological cross-sectional area of the jaw muscles does indeed contribute to the speed of jaw closure in clariid fish.

Animals↗

3D joint dynamics of walking in toddlers A cross-sectional study spanning the first rapid development phase of walking.

This study aims at giving an insight into the causative forces of walking in toddlers. Therefore, joint angle, moment and power profiles of 10 toddlers with less than 6 months of walking experience are compared to the stereotype adult patterns. In general, joint moments are small, which can be explained both by the small size of toddlers and differences in walking strategy. Also mass specific powers are reduced due to the low average walking speed. Balance problems in toddlers lead to a dominance of hip and knee extending moments throughout stance. The joint moment profiles are characterized by a reduced complexity, which might suggest an immature control of movement. Another feature of toddler gait is that virtually no power is generated at the ankle joint prior to foot-off (no active push-off). We also examined the effect of walking experience on the toddler gait pattern. In general, an evolution towards a more mature gait becomes evident after 4 months of independent walking. Changes are observed in step-time parameters, ankle dorsiflexing moment and power absorption at the hip joint.

Ankle↗

Performing the vertical jump: movement adaptations for submaximal jumping.

The purpose of this study was to gain insight into the kinematics and kinetics of the vertical jump when jumping for different heights and to investigate movement effectiveness as a criterion for movement control in submaximal jumping. In order to jump high a countermovement is used and large body segments are rotated, both of which consume energy which is not directly used to gain extra jump height. It was hypothesized that the energy used to reach a specified jump height is minimized by limiting the non-effective energy consumed. Standing vertical jumps attempting 100%, 75%, 50%, and 25% of maximal height were performed by a group of 10 subjects. Force and motion data were recorded simultaneously during each performance. We found that jump height increased due to increasing vertical velocity at take off. This was primarily related to an increase in countermovement amplitude. As such, flexion amplitude of the hip joint increased with jump height whereas the ankle and knee joint flexion did not. These findings revealed that for submaximal jumping a consistent strategy was used of maximizing the contribution of distal joints and minimizing the contribution of proximal joints. Taking into account the high inertia of proximal segments, the potential energy deficit due to countermovement prior to joint extension, the advantageous horizontal orientation of the foot segment during stance and the tendon lengths in distal muscles, it was concluded that movement effectiveness is a likely candidate for the driving criterion of this strategy.

Adaptation, Physiological↗

Mechanical energy in toddler gait. A trade-off between economy and stability?

Mechanical energy expenditure was investigated in children who are just learning to walk and compared with adult mechanical energy expenditure during walking. First, we determined whether the inverted pendulum (IP) mechanism of energy exchange was present in toddlers. It seems that new walkers partially make use of this energy saving mechanism, but it is less efficient than in adults. The reduced recovery values (R=40% at optimal speeds in toddlers compared to 70% in adults) can be explained by their low self-selected walking speed in combination with their tossing gait (large vertical oscillations of the body) and by the observation that during as much as 25-50% of the gait cycle kinetic and potential energy are oscillating in-phase. The second step was to calculate positive external mechanical work (Wext). Since the IP mechanism is less efficient in toddlers, more mass-specific positive work has to be performed to lift and accelerate the centre of mass than in adults walking at the same speed, even when differences in body size are taken into account. The amount of positive internal work (Wint,k) necessary to move the body segments relative to the centre of mass was the third parameter we calculated. In toddlers Wint,k is largely determined by the kinetic energy of the lower limb. Compared to adults, toddlers have to perform less mass-specific work per unit distance to accelerate the body segments since the upper body is kept relatively stiff during walking and there is no arm swing. Apart from work performed on the centre of mass and work performed to move the body segments relative to the centre of mass, when walking some work is also performed during double contact as both legs are pushing against each other. Two methods were used to calculate this amount of work, both leading to the same conclusions. Mass-specific work during double contact is small in toddlers compared to adults because of their low walking speed. Finally the total amount of mechanical work performed in toddlers was compared to the work production observed in adults. Wext seems to be the major determinant for total mechanical energy expenditure. At intermediate froude numbers work production is comparable between adults and toddlers, but at low and high froude numbers Wtot increases due to the steep increases in Wext. Despite the fact that mechanical work requirements in toddler gait are underestimated if work during double contact is not taken into account, it is not a major determinant of the energy cost of walking.

Acceleration↗

Bipedalism in lizards: whole-body modelling reveals a possible spandrel.

This paper illustrates how simple mechanical models based on morphological, ethological, ecological and phylogenetic data can add to discussions in evolutionary biology. Bipedal locomotion has evolved on numerous occasions in lizards. Traits that appear repeatedly in independent evolutionary lines are often considered adaptive, but the exact advantages of bipedal locomotion in lizards remain debated. Earlier claims that bipedalism would increase maximal running speed or would be energetically advantageous have been questioned. Here, we use 'whole body' mechanical modelling to provide an alternative solution to the riddle. The starting point is the intermittent running style combined with the need for a high manoeuvrability characterizing many small lizard species. Manoeuvrability benefits from a caudal shift of the centre of mass of the body (body-COM), because forces to change the heading and to align the body to this new heading do not conflict with each other. The caudally situated body-COM, however, might result in a lift of the front part of the body when accelerating (intermittent style), thus resulting in bipedal running bouts. Based on a momentum-impulse approach the effect of acceleration is quantified for a mechanical model, a virtual lizard (three segments) based on the morphometrics of Acanthodactylus erythrurus (a small lacertid lizard). Biologically relevant input (dimensions, inertial properties, step cycle information, etc.) results in an important lift of the front part of the body and observable distances passively covered bipedally as a consequence of the acceleration. In this way, no functional explanation of the phenomenon of lizard bipedalism is required and bipedalism can probably be considered non-adaptive in many cases. This does not exclude, however, some species that may have turned this consequence to their benefit. For instance, instantaneous manipulation of the position of the centre of the body-COM allows stable, persisting bipedal running. Once this was achieved, the bipedal spandrel could be exploited further.

Acceleration↗

Dynamic plantar pressure distribution during terrestrial locomotion of bonobos (Pan paniscus).

We collected high-resolution plantar pressure distributions of seven bonobos during terrestrial bipedal and quadrupedal locomotion (N = 146). Functional foot length, degree of hallux abduction, and total contact time were determined, and plots, showing pressure as a function of time for six different foot regions, were generated. We also studied five adult humans for comparison (N = 13). Both locomotion types of the bonobo show a large variation in plantar pressure distributions, which could be due to the interference of instantaneous behavior with locomotion and differences in walking speed and body dimensions. The heel and the lateral midfoot typically touch down simultaneously at initial ground contact in bipedal and quadrupedal walking of bonobos, in contrast with the typical heel-strike of human bipedalism. The center of pressure follows a curved course during quadrupedalism, as a consequence of the medial weight transfer during mid-stance. Bipedal locomotion of bonobos is characterized by a more plantar positioning of the feet and by a shorter contact time than during quadrupedal walking, according to a smaller stride and step length at a higher frequency. We observed a varus position of the foot with an abducted hallux, which likely possesses an important sustaining and stabilizing function during terrestrial locomotion.

Animals↗

Pressure distribution patterns under the feet of new walkers: the first two months of independent walking.

In order to describe foot function during the first weeks of independent walking, spatio-temporal pressure distribution patterns were measured. These data give detailed information about roll-off of the foot, by determining the course of the center of pressure, and about load bearing, by calculating relative vertical impulses under the feet. During those first weeks of independent walking, roll-off is very unstable. Although infants can occasionally perform a mature roll-off, a consistent pattern has not yet developed and there is instability. To improve stability the entire plantar surface area contributes to load bearing--first, because a larger contact area will improve stability, and second, because a forward shifting of the load allows more muscular control to compensate for minor imbalances under the foot.

Adult↗

Propulsive impulse as a covarying performance measure in the comparison of the kinematics of swimming and jumping in frogs.

Animals have to modulate their locomotor behavior according to changes in external circumstances. The locomotor requirements are expected to be most extreme for species that move through different physical environments, such as water versus land. In this study, we examine the use of the propulsive impulse as a covariate in the comparison of the kinematics of locomotion of a semi-aquatic frog Rana esculenta, across land and through water. We focused on the propulsive phase because it is functionally the most significant phase of the locomotor cycle in both jumping and swimming, and it is also the most comparable. The frog alters the joint angles of its legs in order to adjust its performance (i.e. impulse) within both locomotor modes. The kinematics and this modulation of the propulsive phase differ between the two modes; however, we found that the impulse ranges of swimming and jumping do not fully overlap. Possible explanations for this include larger lateral forces during swimming, a reduced force transmission due to a lower external load during swimming and reduced muscle recruitment due to differences in coordination patterns.

Animals↗

Performance constraints in decathletes.

Physical performance by vertebrates is thought to be constrained by trade-offs between antagonistic pairs of ecologically relevant traits and between conflicting specialist and generalist phenotypes, but there is surprisingly little evidence to support this reasoning. Here we analyse the performance of world-class athletes in standardized decathlon events and find that it is subject to both types of trade-off, after correction has been made for differences between athletes in general ability across all 10 events. These trade-offs may have imposed important constraints on the evolution of physical performance in humans and other vertebrates.

Animals↗

Segment and joint angles of hind limb during bipedal and quadrupedal walking of the bonobo (Pan paniscus).

We describe segment angles (trunk, thigh, shank, and foot) and joint angles (hip, knee, and ankle) for the hind limbs of bonobos walking bipedally ("bent-hip bent-knee walking," 17 sequences) and quadrupedally (33 sequences). Data were based on video recordings (50 Hz) of nine subjects in a lateral view, walking at voluntary speed. The major differences between bipedal and quadrupedal walking are found in the trunk, thigh, and hip angles. During bipedal walking, the trunk is approximately 33-41 degrees more erect than during quadrupedal locomotion, although it is considerably more bent forward than in normal human locomotion. Moreover, during bipedal walking, the hip has a smaller range of motion (by 12 degrees ) and is more extended (by 20-35 degrees ) than during quadrupedal walking. In general, angle profiles in bonobos are much more variable than in humans. Intralimb phase relationships of subsequent joint angles show that hip-knee coordination is similar for bipedal and quadrupedal walking, and resembles the human pattern. The coordination between knee and ankle differs much more from the human pattern. Based on joint angles observed throughout stance phase and on the estimation of functional leg length, an efficient inverted pendulum mechanism is not expected in bonobos.

Animals↗

Bite performance in clariid fishes with hypertrophied jaw adductors as deduced by bite modeling.

Within clariid fishes several cranial morphologies can be discerned. Especially within anguilliform representatives an increase in the degree of hypertrophy of the jaw adductors occurs. The hypertrophy of the jaw adductors and skeletal modifications in the cranial elements have been linked to increased bite force. The functional significance of this supposed increase in bite force remains obscure. In this study, biomechanical modeling of the cranial apparatus in four clariid representatives showing a gradual increase in the hypertrophy of the jaw adductors (Clarias gariepinus, Clariallabes melas, Channallabes apus, and Gymnallabes typus) is used to investigate whether bite force actually increased. Static bite modeling shows that the apparent hypertrophy results in an increase in bite force. For a given head size, the largest bite forces are predicted for C. apus, the lowest ones for C. gariepinus, and intermediate values are calculated for the other species. In addition, also in absolute measures differences in bite force remain, with C. apus biting distinctly harder than C. gariepinus despite its smaller head size. This indicates that the hypertrophy of the jaw adductors is more than just a correlated response to the decrease in absolute head size. Further studies investigating the ecological relevance of this performance difference are needed.

Animals↗

Variation in speed, gait characteristics and microhabitat use in lacertid lizards.

We quantified four gait characteristics (stride length, stride frequency, step length and floating distance) over a range of running speeds in 11 lacertid lizard species known to vary in maximal sprint speed and microhabitat use. For each species, we measured snout-vent length (SVL), body mass and hindlimb length. We tested which variables determine sprint speed, how each species modulates sprint speed and whether species occurring in different microhabitats differ in speed modulation strategy. In doing so, we aimed to test the assumption that sprint speed is correlated with hindlimb length through its effect on stride length. Variation in maximal sprint speed is determined by variation in both stride length and frequency, but those species that modulate their sprint speed mainly by altering stride length appear to attain the highest maximal speeds. At maximal sprint speed, long-limbed species take larger strides because of the positive effect of hindlimb length on step length and floating distance. However, when hindlimb length is statistically controlled for, mass has a negative effect on step length. None of the three morphological variables explained the interspecific variation in stride frequency at maximal sprint speed. Possibly, differences in physiological properties (e.g. muscle contraction speed) underlie the variation in stride frequency. The 11 species modulate their speed in different ways. Lacertids often seen in vertical microhabitats do not seem to be either pronounced stride length or frequency modulators. These species alter their speed by combining the two strategies. However, species occurring mostly in open and vegetated microhabitats are, respectively, stride length and stride frequency modulators. This difference in running style is substantiated by interspecific morphological differences.

Animals↗

The relationship between speed, contact time and peak plantar pressure in terrestrial walking of bonobos.

The aim of this paper is twofold. Firstly, we investigate whether contact times, as recorded by pedobarographic systems during quadrupedal and bipedal walking of bonobos, can be used to reliably calculate actual velocities, by applying formulae based on lateral-view video recordings. Secondly, we investigate the effect of speed on peak plantar pressures during bipedal and quadrupedal walking of the bonobo. Data were obtained from 4 individuals from a group of bonobos at the Animal Park Planckendael. From our study, we can conclude that both walking speeds calculated from contact times and lower leg length or simply from recorded contact times are good estimators for walking speed, when direct observation of the latter is impossible. Further, it was found that effects of speed on peak plantar pressures and vertical forces are absent or at least subtle in comparison to a large variation in pressure patterns. In bonobos, the same pressure patterns are used at all walking speeds, and, in consequence, we do not expect major changes in foot function.

Analysis of Variance↗