====
Biomechanical innovations are the underpinning of many great transitions in vertebrate evolution. The origin of birds is marked by radical transformations of the braincase, palate, and snout into a kinetic feeding system. New fossil discoveries hint that palate mechanics have played a crucial role in the diversification and success of birds, yet to date, there is no rigorous biomechanical framework for interpreting palate function in birds and other theropod dinosaurs. Here, we use three dimensional (3D) muscle modeling and linkage analysis to elucidate the origins of powered cranial kinesis in avian dinosaurs. Powered cranial kinesis did not evolve until neognaths. This study highlights the importance of integrating biomechanical modeling and phylogenetic methods for understanding key innovations in the origins of major clades.
Abstract
The origin of birds represents a pivotal transition in vertebrate evolution, marked by significant changes in both brain size and feeding biomechanics. The evolution of the avian skull involved dramatic modifications, such as a segmented palate and the development of powered cranial kinesis in neognath birds. Powered kinesis, the ability to move parts of the skull independently, is considered a key innovation behind the dietary diversity and evolutionary success of birds. However, the processes driving the emergence of avian kinesis have remained unclear until recently. By analyzing data from Mesozoic birds, including reinterpretations of palate homology, 3D jaw muscle biomechanics, and linkage analysis, researchers have quantified changes in muscle forces and their effects on palate mechanics during the transition from theropods to birds. As the neurocranium expanded in non-avian theropods, temporal muscles shifted to more rostrocaudal positions in birds, aiding in the segmentation of the pterygoid. This musculoskeletal transformation increased fore-aft muscle force in neognaths, enabling powered cranial kinesis. A critical change was the separation of the epipterygoid ossification from the braincase, leading to the breakdown of primitive kinematic linkages and the development of a new basicranial joint, which allowed for greater cranial flexibility. These findings shed light on how the neurosensory and feeding systems coevolved during bird origins and offer new methods for identifying cranial kinesis in extinct vertebrates.
***
News:
How big brains and flexible skulls led to the evolution of modern birds