Skeletal pneumaticity
Skeletal pneumaticity is the presence of air spaces within bones. It is generally produced during development by excavation of bone by pneumatic diverticula (air sacs) from an air-filled space such as the lungs or nasal cavity. Pneumatization is highly variable between individuals, and bones not normally pneumatized can become pneumatized in pathological development.
Cranial pneumaticity
Pneumatization occurs in the skulls of mammals, crocodilians and birds among extant tetrapods. Pneumatization has been documented in extinct archosaurs including dinosaurs and pterosaurs. Pneumatic spaces include the paranasal sinuses and some of the mastoid cells.
Postcranial pneumaticity
Postcranial pneumaticity is found largely in certain archosaur groups, namely dinosaurs,[1] pterosaurs, and birds. Vertebral pneumatization is widespread among saurischian dinosaurs, and some theropods have quite widespread pneumatization -- Aerosteon riocoloradensis has pneumatization of the ilium, furcula, and gastralia as well.[2] Many modern birds are extensively pneumatized. The air pockets of the bones are connected to the pulmonary air sacs:[3]
| Air sacs | Skeleton portion pneumatized by their divercula |
|---|---|
| cervical air sacs | cervical and anterior thoracic vertebrae |
| abdominal air sacs | posterior thoracic vertebrae, synsacrum and hindlimb |
| interclavicular air sac | sternum, sternal ribs, coracoid, clavicle, scapula, and forelimb |
| anterior and posterior thoracic air sacs | - (lack diverticula) |
However the extent of pneumaticity depends on species. For example it is slight in diving birds, loons lack pneumatic bones at all.[3][4]
Postcranial pneumatization is rarer outside of Archosauria. Examples include the hyoid in howler monkeys Alouatta, and the dorsal vertebrae in the osteoglossiform fish Pantodon.[5] Slight pneumatization of the centra and rib heads by dorsal diverticula in the lungs of land tortoises has also been documented.[5] In addition, pathological pneumatization has been known to occur in the human atlas vertebra.[6]
Function of skeletal pneumaticity
The exact function of skeletal pneumaticity is not definitively known, but there are several working hypotheses concerning the role of skeletal pneumaticity in an organism.
Reduce body mass
By invading the bones, the pneumatic diverticula would replace marrow with air, reducing the overall body mass. Reducing the body mass would make it easier for pterosaurs and birds to fly as there is less mass to keep aloft with the same amount of muscle powering the flight strokes.[7] Pneumatizing the vertebral column of sauropods would reduce the weight of these organisms, and make it easier to support and move the massive neck.[1]
Alter skeletal mass distribution
Skeletal pneumaticity allows animals to redistribute the skeletal mass within their body. The skeletal mass of a bird (pneumatized) and a mammal (not pneumatized) with similar body size is roughly the same, yet the bones of birds were found to be denser than the bones of mammals. This suggests that pneumatization of bird bones does not affect the overall mass but allows for a better balance of weight within the body to allow for greater balance, agility and ease of flight.[8]
Balance
In theropods, the head and neck are greatly pneumatized, and the forearms are reduced. This would help reduce the mass further away from the center of balance. This adjustment to the center of mass would allow the animal to reduce its rotational inertia, thereby increasing its agility. The sacral pneumaticity would lower its center of mass to a more ventral position, allowing it more stabilization.[5]
Adaptation for high altitude
Screamers are highly pneumatized birds with pneumatic diverticula traveling throughout the bones and into the skin. As screamers fly at high altitudes, it is hypothesized that the extreme pneumaticity in these birds is indicative of an adaptation for flying in high altitudes.[9]
References
- 1 2 Wedel, M.J. 2005. Postcranial skeletal pneumaticity in sauropods and its implications for mass estimates; pp. 201–228 in Wilson, J.A., and Curry-Rogers, K. (eds.), The Sauropods: Evolution and Paleobiology. University of California Press, Berkeley. (link)
- ↑ Sereno, P.C., Martinez, R.N., Wilson, J.A., Varricchio, D.J., Alcober, O.A., Larsson, H.C.E. 2008. Evidence for avian intrathoracic air sacs in a new predatory dinosaur from Argentina. PLoS ONE 3(9): e3303. doi:10.1371/journal.pone.0003303 link
- 1 2 Wedel, Mathew J. (2003). "Vertebral pneumaticity, air sacs, and the physiology of sauropod dinosaurs" (PDF). Paleobiology. The Paleontological Society. 29 (2): 243–255. doi:10.1666/0094-8373(2003)029<0243:vpasat>2.0.co;2. Retrieved 2014-01-21. External link in
|publisher=(help) - ↑ Schorger, A. W. (September 1947). "The deep diving of the loon and old-squaw and its mechanism" (PDF). The Wilson Bulletin. The Wilson Ornithological Society. 59 (3): 151–159. Retrieved 2014-01-21. External link in
|publisher=(help) - 1 2 3 Farmer, C.G. 2006. On the Origin of Avian Air Sacs. Resp. Physiol. Neuro. 154(1–2):89–106.
- ↑ Bruno Moreira and Peter M. Som. Unexplained Extensive Skull Base and Atlas Pneumatization: Computed Tomographic Findings. Arch Otolaryngol Head Neck Surg, Jul 2010; 136: 731 - 733.
- ↑ Bennett, Christopher (2001). "The Osteology and Functional Morphology of the Late Cretaceous Pterosaur Pteranodon". Palaeontographica Abteilung A: 1–153.
- ↑ Dumont, Elizabeth R. (2010-07-22). "Bone density and the lightweight skeletons of birds". Proceedings of the Royal Society of London B: Biological Sciences. 277 (1691): 2193–2198. doi:10.1098/rspb.2010.0117. ISSN 0962-8452. PMC 2880151
. PMID 20236981. - ↑ Picasso, Mariana BJ; Mosto, Maria Clelia; Tozzi, Romina; Degrange, Federico J; Barbeito, Claudio G (2014). "A peculiar association: the skin and the subcutaneus diverticula of the Southern Screamer (Chauna torquata, Anseriformes)". Vertebrate Zoology. 64 (2): 245–249.