We provide the first predictions of bite force (B S ) in a wide sample of living and fossil mammalian predators. To compare between taxa, we calculated an estimated bite force quotient (BFQ) as the residual of B S regressed on body mass. Estimated B S adjusted for body mass was higher for marsupials than placentals and the Tasmanian devil (Sarcophilus harrisii) had the highest relative B S among extant taxa. The highest overall B S was in two extinct marsupial lions. BFQ in hyaenas were similar to those of related, nonosteophagous taxa challenging the common assumption that osteophagy necessitates extreme jaw muscle forces. High BFQ in living carnivores was associated with greater maximal prey size and hypercarnivory. For fossil taxa anatomically similar to living relatives, BFQ can be directly compared, and high values in the dire wolf (Canis dirus) and thylacine (Thylacinus cynocephalus) suggest that they took relatively large prey. Direct inference may not be appropriate where morphologies depart widely from biomechanical models evident in living predators and must be considered together with evidence from other morphological indicators. Relatively low BFQ values in two extinct carnivores with morphologies not represented among extant species, the sabrecat, Smilodon fatalis, and marsupial sabretooth, Thylacosmilus atrox, support arguments that their killing techniques also differed from extant species and are consistent with 'canineshear bite' and 'stabbing' models, respectively. Extremely high BFQ in the marsupial lion, Thylacoleo carnifex, indicates that it filled a large-prey hunting niche.
The mammalian skull has proven to be remarkably plastic during ontogeny and phylogeny in response to the demands of mastication. I examine whether the bending strength of the skull in some mammals correlates with the maximal loads imposed through the masticatory apparatus. The approach is analytical, using the methods of beam theory. Cranial strength is estimated from the second moment of area and other geometrical measurements made from 20–30 transverse CT scans through the skulls of 20 opossums (Didelphis virginiana), and through single skulls of five felid and five canid genera of different sizes. Maximal biting forces were first estimated from areas on the dried skulls bounding the spaces filled in life by the jaw-adducting muscles. These estimates were then adjusted with reference to forces recorded in vivo or, for other specimens, to estimates based on dissections of the jaw muscles. Stress distribution in the face, and peak stresses, were calculated for each animal. Stress levels are low (5–35 MPa) compared with peak stresses in limb bones (40–100 MPa), which correlates with the lower in vivo strains in cranial bones reported in the literature. Stress estimates are in a range that is plausible, which supports the validity of the procedure. Patterns of stress distribution along the face are comparable within each group of animals. Peak stress is independent of size for the carnivorans, but decreases with increasing skull length in D. virginiana. High bending strength of the skull is a consequence of cranial form in mammals; having to enclose the brain, for example, increases the bending strength of the skull. Furthermore, factors such as stiffness or shear and torsional strength may be more important than bending strength. However, bending stress levels appear to be closely regulated, as in other bones that have been studied. The threshold for optimising bending strength and weight is simply at a different level.
Finite element analysis (FEA) is used by industrial designers and biomechanicists to estimate the performance of engineered structures or human skeletal and soft tissues subjected to varying regimes of stress and strain. FEA is rarely applied to problems of biomechanical design in animals, despite its potential to inform structure-function analysis. Non-invasive techniques such as computed tomography scans can be used to generate accurate three-dimensional images of structures, such as skulls, which can form the basis of an accurate finite element model. Here we have applied this technique to the long skull of the large carnivorous theropod dinosaur Allosaurus fragilis. We have generated the most geometrically complete and complex FEA model of the skull of any extinct or extant organism and used this to test its mechanical properties and examine, in a quantitative way, long-held hypotheses concerning overall shape and function. The combination of a weak muscle-driven bite force, a very 'light' and 'open' skull architecture and unusually high cranial strength, suggests a very specific feeding behaviour for this animal. These results demonstrate simply the inherent potential of FEA for testing mechanical behaviour in fossils in ways that, until now, have been impossible.
Estimates of biting forces are widely used in paleontological and comparative studies of feeding mechanics and performance, and are usually derived from lever models based on measurements made on the skull that are relevant to the mechanics of the masticatory system. Owing to assumptions and unmeasurable errors in their estimation, such values are used comparatively rather than as absolute estimates. The purpose of this paper was to provide calibration of post-mortem calculated bite force estimates by comparing them to in vivo forces derived from a sample of 20 domestic dogs ( Canis familiaris ) during muscle stimulation under general anaesthesia. Two lever models previously described in the literature were used to estimate post-mortem values, and regression analysis was also performed to derive best-fit equations against a number of morphometric measurements on the skull. The ranges of observed forces in vivo were 147-946 N at the canine, and 524-3417 N at the second molar. The lever models substantially underestimated these forces, giving mean values between 39% and 61% of the observed means. Predictability was considerably improved by removing the linear bias and deviation of the regression slope from unity with an adjustment equation. Best-fit statistical models developed on these animals performed considerably better (calculated means within 0.54% of observed means) and included easily measureable variables such as bodyweight, dimensions of the temporalis fossa and out-lever from the jaw joint to the biting tooth. These data should lead to more accurate absolute, rather than relative, estimates of biting forces for other extant and fossil canids, and other carnivorans by extrapolation.
These findings provided a basis for further experimental studies to identify specific mechanisms of various types of injury in dogs that participate in agility activities.
Specific factors were associated with agility-related injuries in dogs. Educational prevention strategies should target at-risk populations in an effort to reduce potential injuries. Future research should focus on the biomechanical factors associated with agility-related injuries.
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