Abstract

Anatomical traits associated with locomotion often exhibit specializations for ecological niche, suggesting that locomotor specializations may constitute selective regimes acting on limb skeletal traits. To test this, I sampled 42 species of Mustelidae, encompassing climbing, digging, and swimming specialists, and determined whether trait variation reflects locomotor specialization by performing a principal components analysis on 14 forelimb traits. In addition to Brownian motion models, three Ornstein–Uhlenbeck models of selective regimes were applied to PC scores describing trait variation among mustelids: one without a priori defined phenotypic optima, one with optima based upon locomotor habit, and one with a single phenotypic optimum. PC1, which explained 43.8% of trait variance, represented a trade‐off in long bone gracility and deltoid ridge length vs. long robustness and olecranon process length and distinguished between climbing specialists and remaining mustelids. PC2, which explained 17.4% of trait variance, primarily distinguished the sea otter from other mustelids. Best fitting trait diversification models are selective regimes differentiating between scansorial and nonscansorial mustelids (PC1) and selective regimes distinguishing the sea otter and steppe polecat from remaining mustelids (PC2). Phylogenetic half‐life values relative to branch lengths suggest that, in spite of a strong rate of adaptation, there is still the influence of past trait values. However, simulations of likelihood ratios suggest that the best fitting models are not fully adequate to explain morphological diversification within extant mustelids.

Highlights

  • Given the forelimb’s importance for the differing locomotor habits of mustelids, I predict that a model of adaptive diversification according to locomotor specialization is the most likely model of morphological diversification for the mustelid forelimb

  • In the unconstrained Ornstein– Uhlenbeck (OU) model for PC2, shifts in phenotypic optima occur at roughly 40% of the length of branches leading to the sea otter (Enhydra lutris; posterior probability = 0.97) and the steppe polecat (Mustela eversmanii; posterior probability = 0.25)

  • Fossorial and natatorial mustelids, while seeming to occupy somewhat distinct regions of phenotypic space, fall under one selective regime along with generalized mustelids. These results suggest that evolution of the forelimb skeleton under a single phenotypic optimum can facilitate multiple locomotor specializations among mustelids

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Summary

| INTRODUCTION

Locomotion is fundamental to vertebrate biology, and anatomists have long noted that in many vertebrate taxa, mammals Mustelidae are an ecologically diverse clade within Carnivora, having scansorial/climbing, fossorial/digging, and natatorial/swimming specialists, in addition to more generalized taxa (Holmes, 1980; Schutz & Guralnick, 2007). Among all the locomotor specializations exhibited by mustelids, the forelimbs play an important role, whether it is in digging (Hildebrand, 1985b; Moore, Budny, Russell, & Butcher, 2013; Rose, Moore, Russell, & Butcher, 2014), swimming (Fish, 1994; Williams, 1983a), climbing (Fabre et al, 2013b; Leach, 1977), or terrestrial ­locomotion (Gambaryan, 1974; Horner & Biknevicius, 2010; Williams, 1983b). Given the forelimb’s importance for the differing locomotor habits of mustelids, I predict that a model of adaptive diversification according to locomotor specialization is the most likely model of morphological diversification for the mustelid forelimb

| MATERIALS AND METHODS
| DISCUSSION
20 Half-life values PC1
Findings
| CONCLUSIONS
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