ArticleProceedings of the National Academy of Sciences of the United States of America2025
Avian cranial kinesis is the result of increased encephalization during the origin of birds.
Article in Proceedings of the National Academy of Sciences of the United States of America, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.
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Who cites it
5 citing papers in PubMed.
- Beyond mammals: the evolution of chewing and other forms of oropharyngeal food processing in vertebrates.Biological reviews of the Cambridge Philosophical Society · 2026Review
- Shouldering the challenge of deciphering avian palate evolution.Proceedings of the National Academy of Sciences of the United States of America · 2026Article
- Reply to Benito et al.: Problems in the Cretaceous evolution of the avian palatobasal joint.Proceedings of the National Academy of Sciences of the United States of America · 2026Article
- Dinosaur skull geometry does not follow functional optimization trends but facilitates adaptability.iScience · 2025Article
- Avian cranial kinesis is the result of increased encephalization during the origin of birds.Proceedings of the National Academy of Sciences of the United States of America · 2025Article
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7 authors.
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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.
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