37 research outputs found

    Tibiofemoral Contact Forces in the Anterior Cruciate Ligament-Reconstructed Knee.

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    PURPOSE: To investigate differences in ACL reconstructed (ACLR) and healthy individuals in terms of the magnitude of the tibiofemoral contact forces, as well as the relative muscle and external load contributions to those contact forces, during walking, running and sidestepping gait tasks. METHODS: A computational electromyography-driven neuromusculoskeletal model was used to estimate the muscle and tibiofemoral contact forces in those with combined semitendinosus and gracilis tendon autograft ACLR (n=104, 29.7±6.5 years, 78.1±14.4 kg) and healthy controls (n=60, 27.5±5.4 years, 67.8±14.0 kg) during walking (1.4±0.2 ms), running (4.5±0.5 ms) and sidestepping (3.7±0.6 ms). Within the computational model, the semitendinosus of ACLR participants was adjusted to account for literature reported strength deficits and morphological changes subsequent to autograft harvesting. RESULTS: ACLRs had smaller maximum total and medial tibiofemoral contact forces (~80% of control values, scaled to bodyweight) during the different gait tasks. Compared to controls, ACLRs were found to have a smaller maximum knee flexion moment, which explained the smaller tibiofemoral contact forces. Similarly, compared to controls, ACLRs had both a smaller maximum knee flexion angle and knee flexion excursion during running and sidestepping, which may have concentrated the articular contact forces to smaller areas within the tibiofemoral joint. Mean relative muscle and external load contributions to the tibiofemoral contact forces were not significantly different between ACLRs and controls. CONCLUSION: ACLRs had lower bodyweight-scaled tibiofemoral contact forces during walking, running and sidestepping, likely due to lower knee flexion moments and straighter knee during the different gait tasks. The relative contributions of muscles and external loads to the contact forces were equivalent between groups

    Plasma Sources in Planetary Magnetospheres: Mercury

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    Ontogeny of predator-sensitive foraging and routine metabolism in larval shorthorn sculpin, Myoxocephalus scorpius

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    Most animals will reduce foraging activity in the presence of a predatory threat. However, little is known about the onset of this decision-making ability during the early life stages of fishes, and how the trade-off between foraging and predator-avoidance may be affected by changes in metabolic demand during ontogeny. To examine these issues, the foraging behaviour of larval shorthorn sculpin Myoxocephalus scorpius was monitored during visual exposure to a predatory threat (juvenile Atlantic cod, Gadus morhua) throughout development at 3°C (March–April, 2004). Larvae did not respond to predatory exposure during the first week post-hatch, but thereafter showed drastic reductions in foraging activity when exposed to predators. During early development, the mass-specific routine metabolism of shorthorn sculpin larvae displayed a triphasic ontogeny and peaked during metamorphosis. This high mass-specific metabolic demand could make reduced foraging under predation threat very costly during this stage of development. To further investigate this possibility, additional experiments were performed (March–April, 2005) where larvae were reared with visual exposure to predators for 6 h day−1 during the feeding period. At 7-week post-hatch, larvae exposed to predators were smaller (wet mass and SL), showed decreased levels of whole-body lipids and certain fatty acids, and experienced higher rates of mortality as compared to control larvae. In environments where abundant predators cause larval fish to reduce their foraging rate, growth and survival of larvae may be negatively affected

    The effect of prey density on foraging mode selection in juvenile lumpfish: balancing food intake with the metabolic cost of foraging

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    <p>1: In many species, individuals will alter their foraging strategy in response to changes in prey density. However, previous work has shown that prey density has differing effects on the foraging mode decisions of ectotherms as compared with endotherms. This is likely due to differences in metabolic demand; however, the relationship between metabolism and foraging mode choice in ectotherms has not been thoroughly studied.</p> <p>2:Juvenile lumpfish Cyclopterus lumpus forage using one of two modes: they can actively search for prey while swimming, or they can ‘sit-and-wait’ for prey while clinging to the substrate using a ventral adhesive disk. The presence of these easily distinguishable foraging modes makes juvenile lumpfish ideal for the study of foraging mode choice in ectotherms.</p> <p>3: Behavioural observations conducted during laboratory experiments showed that juvenile lumpfish predominantly use the ‘cling’ foraging mode when prey is abundant, but resort to the more costly ‘swim’ mode to seek out food when prey is scarce. The metabolic cost of active foraging was also quantified for juvenile lumpfish using swim-tunnel respirometry, and a model was devised to predict the prey density at which lumpfish should switch between the swim and cling foraging modes to maximize energy intake.</p> <p>4: The results of this model do not agree with previous observations of lumpfish behaviour, and thus it appears that juvenile lumpfish do not try to maximize their net energetic gain. Instead, our data suggest that juvenile lumpfish forage in a manner that reduces activity and conserves space in their limited aerobic scope. This behavioural flexibility is of great benefit to this species, as it allows young individuals to divert energy towards growth as opposed to activity. In a broader context, our results support previous speculation that ectotherms often forage in a manner that maintains a minimum prey encounter rate, but does not necessarily maximize net energy gain.</p&gt

    MESSENGER: Exploring Mercury’s Magnetosphere

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