Neurocranium

Other animals

The neurocranium is formed by the combination of the endocranium, the lower portions of the cranial vault, and the skull roof. Through the course of evolution, the human neurocranium has expanded from comprising the back part of the mammalian skull to being also the upper part: during the evolutionary expansion of the brain, the neurocranium has overgrown the splanchnocranium. The upper-frontmost part of the cranium also houses the evolutionarily newest part of the mammal brain, the frontal lobes.

In other vertebrates, the foramen magnum is oriented towards the back, rather than downwards. The braincase contains a greater number of bones, most of which are endochondral rather than dermal:

• The singular basioccipital is the rear lower part of the braincase, below the foramen magnum. It is homologous to the basilar part of the occipital bone. In the ancestral tetrapod, the basioccipital makes up most of a large central knob-like surface, the occipital condyle, which articulates with the vertebrae as a ball-and-socket joint. This plesiomorphic ("primitive") state is retained by modern reptiles and birds. The underside of the basioccipital may have a pair of large projections which act as neck muscle attachments: the basitubera (also known as basioccipital tubera or basal tubera)
• The paired exoccipitals (singular: exoccipital) are visible at the rear of the braincase, adjacent to the foramen magnum and above the basioccipital. They are homologous to the lateral parts of the occipital bone. Modern amphibians and mammals have independently acquired inflated exoccipitals, acting as paired occipital condyles while the basioccipital is reduced and loses its connection to the vertebrae.
• The singular supraoccipital is the rear upper part of the braincase, above the foramen magnum and below or behind the parietals or postparietals. It is homologous to the squamous part of the occipital bone, which is greatly enlarged in humans.
• The paired opisthotics (singular: opisthotic) form most of the rear lateral part of the braincase, in front of the exoccipitals and above the foramen ovale. They also contribute to the paroccipital process, a lateral projection which acts as a buttress between the braincase and the outer skull bones. In many tetrapods, the opisthotic is fused to its corresponding exoccipital. The jugular foramen is usually found near the point of fusion.
• The paired prootics (singular: prootic) form the lateral part of the braincase, in front of the opisthotics. The front edge of the prootic is typically deeply notched by the exit hole for the trigeminal nerve (V). Many other nerve exits are scattered among the prootic, opisthotic, and exoccipital. The prootic is homologous to the petrous part of the temporal bone (in humans) or the petrosal bone (in other mammals).
• Some reptiles have a laterosphenoid in front of the prootic. This bone is present in archosaurs and other archosauriforms; non-homologous bones in similar locations are known in stem-turtles and some squamates, lissamphibians, and actinopterygian fishes.
• The singular basisphenoid forms the front lower part of the braincase, in front of the basioccipital and below the prootics. Each side of the basisphenoid hosts a basipterygoid process, a lateral rod which bends down and out to link to the pterygoid bones of the bony palate. The basisphenoid may also act as a component of the basitubera.
• The singular parasphenoid is one of the few dermal components of the braincase, a flat plate below the basisphenoid. The parasphenoid acts as a component of the bony palate, wedging between the pterygoid bones and often ornamented with small tooth-like denticles. In many vertebrates the parasphenoid and basisphenoid are fused into a single bone, the parabasisphenoid. The front part of the parabasisphenoid is a blade-like structure, the cultriform process, which extends much further forward than the rest of the braincase.

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