| Session |
Author(s) |
Title |
36 |
Kilbourne, BM |
Functional morphology and diversification of the mustelid hindlimb skeleton and potential influence of differing limb functions |
36 |
Corn, KA*; Friedman, ST; Martinez, CM; Larouche, O; Price, SA; Wainwright, PC |
Feeding mode underlies the major axis of body shape diversity in reef fishes |
36 |
Larouche, O*; Gartner, SM; Westneat, MW; Evans, KM |
The parrotfish beak leads to shifts in cranial integration patterns and increased morphological disparity |
36 |
Alencar, LRV*; Friedman, ST; Wainwright, PC; Price, SA |
How fishes change their size and how such changes impact clade-level dynamics |
36 |
Larouche, O; Hodge, JR; Alencar, LRV; Camper, B; Adams, DS; Zapfe, K; Friedman, ST; Wainwright, PC; Price, SA* |
Does pharyngognathy unlock body shape diversification in acanthomorph fishes? |
36 |
Wynd, BM*; Uyeda, JC |
Absolute fitness explains evolutionary patterns at the micro and macro levels |
36 |
Pevsner, SK*; Grossnickle, DM; Luo, Z-X |
Forelimb functional diversity in Didelphimorphia and Diprotodontia is not strongly limited by developmental constraints |
36 |
Atake, OJ*; Eames, BF |
Tesseral development provides insights into evolution of mineralization patterns in jawed vertebrates |
36 |
Vaz, DB*; Hilton, EJ |
Stick together and act as if you belong: ontogeny and evolution of gill arches of Batrachoidiformes |
36 |
Childers, JL*; Bowie, RCK |
Evolution of elaborate nest design in the Old World weavers (Ploceidae) |
