Studies linking postcranial morphology with locomotion in mammals are common. However, such studies are mostly restricted to caviomorphs in rodents. We present here data from various families, belonging to the three main groups of rodents (Sciuroidea, Myodonta, and Ctenohystrica). The aim of this study is to define morphological indicators for the astragalus and calcaneus, which allow for inferences to be made about the locomotor behaviours in rodents. Several specimens were dissected and described to bridge the myology of the leg with the morphology of the bones of interest. Osteological characters were described, compared, mechanically interpreted, and correlated with a “functional sequence” comprising six categories linked to the lifestyle and locomotion (jumping, cursorial, generalist, fossorial, climber and semi-aquatic). Some character states are typical of some of these categories, especially arboreal climbers, fossorial and “cursorial-jumping” taxa. Such reliable characters might be used to infer locomotor behaviours in extinct species. Linear discriminant analyses (LDAs) were used on a wider sample of species and show that astragalar and calcaneal characters can be used to discriminate the categories among extant species whereas a posteriori inferences on extinct species should be examined with caution.

Rodentia is a species-rich group with diversified modes of life and diets. Although rodent skull morphology has been the focus of a voluminous literature, the functional significance of its variations has yet to be explored in live animals. Myomorphous rodents, including murids, have been suggested to represent "high-performance generalists." We measured in vivo bite force in 14 species of wild and lab-reared murid rodents of various sizes and diets to investigate potential morphofunctional differences between them. We dissected their skulls and computed a biomechanical model to estimate bite force. We first tested if our model allowed good estimation of in vivo data. Then, using morphological, in vivo and estimated bite force data in a phylogenetic context, we aimed to find the drivers of bite force differences among species. Estimated and in vivo bite forces were strongly correlated, which indicates that (a) biomechanical models allow a good estimation of real performance, and that (b) size and muscular changes (increased mass, fiber length, and PCSA) are the main drivers of bite performance differences. Myomorphous rodents, therefore, may have evolved high bite force through a combination of changes in size and musculature, which gave them a great versatility in their ability to process food. We found mixed results at the intraspecific level, with only some species displaying a good fit between estimated and in vivo measurements. We suggest that limited variation in size and muscular organization, and increased behavioral variation might decrease the precision of bite force estimates within species. Anat Rec, 301:256-266, 2018. © 2018 Wiley Periodicals, Inc.

Differences in biological performance, at both intra- and inter-specific levels, have often been linked to morphology but seldom to behavioural or genotypic effects. We tested performance at the intraspecific level by measuring bite force in the African pygmy mouse, Mus minutoides. This species displays an unusual sex determination system, with sex-reversed, X*Y females carrying a feminizing X* chromosome. X*Y females cannot be differentiated from XX females based on external or gonadal morphology; however, they are known to be more aggressive. We found that bite force was higher in X*Y females than in other females and males. We then performed geometric morphometric analyses on their skulls and mandibles and found that the higher performance of X*Y females was mainly explained by a greater overall skull size. The effects of the X* chromosome thus go beyond feminization, and extend to whole-organism performance and morphology. Our results also suggest limited effects of behaviour on bite force.

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Conodonts are among the first vertebrates to have evolved mineralized tooth-like structures. Among these, the so-called P1 elements are known to have been used to break down food and display a wide variety of morphologies. In particular, the repeated independent evolution of platform-like P1 elements have been suggested to correspond to similar functional constraints linked to diet. To test this hypothesis of convergence, we measured size (as element length) for various conodont taxa and used it as a proxy for trophic level. We then tested the correlation between size and platform presence/absence, both on raw data and in a phylogenetic context. Retaining or excluding the platform traits from the character matrix has limited impact on the resulting phylogeny. Contrary to platform presence/absence, size shows no phylogenetic signal. Using the raw data, size and platform presence appear positively correlated. That correlation, however, is no longer significant if one corrects for the phylogeny. We conclude that platform presence cannot be explained by an enlargement of the conodont element, be it via a trophic-level change or developmental constraints. This suggests that conodonts as a whole, and in particular platform-bearing conodonts, were an ecologically diverse group and that the various known platform types are likely to reflect different, rather than convergent, ecological niches.

Murine rodents display a unique cranial morphology and masticatory musculature. Yet detailed myological descriptions are scarce, especially considering the great diversity of the subfamily and the use of the house mouse and brown rat as model organisms. The masticatory musculature in these two species has been thoroughly described, which allows comparisons with other wild species. Description and comparison of a wide range of species constitutes a necessary step to fully understand how ecological factors may influence the morphology and myology of the skull in the Murinae and vice versa. In this study, we describe the masticatory musculature of five mouse species: Mus caroli, Mus cervicolor, Mus pahari, Mus fragilicauda, and Mus minutoides. For each species, one to five specimens were dissected, and their muscle weights and volumes calculated. One specimen was selected for iodine-enhanced CT-scanning, which allowed us to digitally reconstruct the musculature. We then compared the different masticatory arrangements between these species, as well as with the previous descriptions of the house mouse and brown rat. We show that interspecific differences especially involved the temporalis muscle and zygomatico-mandibularis muscular groups, although some differences were also seen in the pterygoid muscle and masseter muscle groups. We then propose some ecological interpretations for these differences, by interpreting them in terms of functional differences.

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