Locomotor, ecological and phylogenetic drivers of skeletal proportions in frogs.

Frogs exhibit complex anatomical features of the pelvis, limbs and spine, long assumed to represent specialisations for jumping. Yet frogs employ a wide range of locomotor modes, with several taxa featuring primary locomotor modes other than jumping. Using a combination of techniques (CT imaging and 3D visualization, morphometrics, phylogenetic mapping), this study aims to determine the link between skeletal anatomy and locomotor style, habitat type and phylogenetic history, shedding new light on how functional demands impact morphology. Body and limb measurements for 164 taxa from all the recognised anuran families are extracted from digitally segmented CT scans of whole frog skeletons and analysed using various statistical techniques. We find that the expansion of the sacral diapophyses is the most important variable for predicting locomotor mode, which was more closely correlated with frog morphology than either habitat type or phylogenetic relationships. Predictive analyses suggest that skeletal morphology is a useful indicator of jumping but less so for other locomotor modes, suggesting that there is a wide range of anatomical solutions to performing locomotor styles such as swimming, burrowing or walking.

Mapping the evolution of accurate Batesian mimicry of social wasps in hoverflies.

Hoverflies (Diptera: Syrphidae) provide an excellent opportunity to study the evolution of Batesian mimicry, where defenseless prey avoid predation by evolving to resemble defended "model" species. Although some hoverflies beautifully resemble their hymenopteran models, others seem to be poor mimics or are apparently nonmimetic. The reasons for this variation are still enigmatic despite decades of research. Here, we address this issue by mapping social-wasp mimicry across the phylogeny of Holarctic hoverflies. Using the "distance transform" technique, we calculate an objective measure of the abdominal pattern similarity between 167 hoverfly species and a widespread putative model, the social wasp, Vespula germanica. We find that good wasp mimicry has evolved several times, and may have also been lost, leading to the presence of nonmimics deep within clades of good mimics. Body size was positively correlated with similarity to the model, supporting previous findings that smaller species are often poorer mimics. Additionally, univoltine species were less accurate wasp mimics than multivoltine and bivoltine species. Hence, variation in the accuracy of Batesian mimics may reflect variation in the opportunity for selection caused by differences in prey value or signal perception (influenced by body size) and phenology or generation time (influenced by voltinism).