Post-canine megadontia

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Post-canine megadontia is an enlargement of the molars and premolars, which is found in early hominid ancestors such as Paranthropus aethiopicus.[1]

Archaeological Evidence[edit]

Paranthropus boisei (left) vs. Homo sapiens (right). The average post-canine tooth area for P. boisei was 756mm2 versus 334mm2 in H. sapiens.[2]

The evidence for post-canine megadontia comes from measuring post-canine tooth surface area of hominid specimens that have been found and comparing these numbers between hominid species. Australopithecus, dated to have lived 2 to 3 million years ago, is the earliest hominid genus to demonstrate post-canine enlargement, with average post-canine tooth area ranging from approximately 460mm2 and going all the way up to the largest tooth area, 756mm2, which is seen in Paranthropus boisei .[2][3] After Australopithecus, a trend of steady decline in post-canine size is observed, starting in the Homo genus and culminating with Homo sapiens which has an average post-canine tooth area of only 334mm2.[2][4]

Studies of premolar size in hominid species that predate Australopithecus afarensis show long, uni-cuspid teeth at the P3 location, while species dated after A. afarensis have been shown to have wider, bicuspid teeth at the same location, which is hypothesized to show the beginnings of canine to premolar evolution in hominids.[5]

Homo floresiensis, a hominid species from the late Pleistocene found in cave deposits in Liang Bua, Indonesia, shows a smaller molar size that is closer to the hominid lineage. However, the remaining teeth of H. floresiensis show similarities to the bigger tooth sizes of the earlier genera Australopithecus and Homo.[6]

Timeline and Map[edit]

A timeline depicting observed evidence of post-canine megadontia

The shift towards post-canine megadontia dates back to about 4-5 million years ago with the discovery of Ardipithecus ramidus in the Middle Awash region of Ethiopia.[7] Distinctive features in A. ramidus such as dentition with reduced canines, the skull, hindlimb and forelimb suggest it to be near the split between the chimpanzee and hominin lineages.[8]

It was the origin of Australopithecus africanus, found in several regions of South Africa (Taung, Sterkfontein, Makapansgat) 2-3 million years ago that first demonstrated the enlargement of the pre-molars and molars. In terms of morphology, A. africanus shares many similar characteristics with A. afarensis as well as other genera in Paranthropus.[9]

The first specimen of Paranthropus aethiopicus was discovered in Lake Turkana, Kenya and its successor, Paranthropus robustus, was found in the northern parts of South Africa (Swartkrans, Kromdraai and Drimolen).[10] Paranthropus boisei, the last species included in the genus Paranthropus, was first found in Olduvai Gorge, Tanzania and around Ethiopia and Kenya.[11] P. boisei was known for massive facial and dental bones and structure, primarily larger mandibles, molars, and premolars, which was an adaptation allowing them to consume hard plant foods with the ability of high force chewing.[11]

A map depicting the locations of species with post-canine megadontia in Africa

The first species in the genus Homo, Homo habilis, has been found in Tanzania and Kenya at sites dating between 2.1 and 1.5 million years ago.[12] Species within the genus Homo showed no difference within molar size up until Homo floresiensis, where smaller molars were beginning to be expressed.[13] Species after H. floresiensis such as H. heidelbergensis, H. neanderthalensis, and H. sapiens began to show instead wider frontal teeth and a decrease in size of the molars compared to earlier species.[14][15][16] H. sapiens shows significantly smaller molars, mandible, and a prominence of the chin.[16]

Evolutionary Implications[edit]

Postcanine megadontia is commonly associated with the repeated consumption of tough plant-like material, which can be referred to as "low-quality food stuffs".[17][18] The substances were integral to the diet of extinct hominids, and their molars were subject to the constant occlusal attrition from the stress of vigorous mastication.[19] The development and evolution of this trait was characterized by a thick coating of enamel surrounding the molars and premolars, mitigating the detrimental effects of the tough diet.[20] As such, this postcanine dentition is capable of “crushing and grinding” the tough shoots and leaves common to the diet of an early hominid.[21] Australopithecus Paranthropus, for example, was perhaps the most noteworthy hominid to display this trait, an adaptation perhaps due to its varied and encompassing diet .[18] Note, postcanine megadontia is hypothesized to have no correlation to durophagy, but is rather a crucial development in hominids that allowed for preservation of occlusal quality.[17]

Increased postcanine size can be correlated with the evolution of other physiological traits [18] [22] [23] [24] Inverse trends of brain mass and molar size point to diet and food processing as a linking factor; encephalization is a crucial consideration in the development of tool usage and extraoral food processing that was observed in Homo species, but not in Australopithecines.[18] Post canine enlargement has also been significantly positively correlated with basal metabolic rate, independently of body size.[22] Larger primates tend to need larger teeth to process more food to meet the energy requirements of a larger body,[23] but the evolution of postcanine megadontia is more likely due to the quality of the diet. The tough, “low-quality food stuffs" consumed by robust Australopithecines, coupled with their lack of food processing technology, lead to an enlargement of the occlusal surface of the molars.[18] [22] [24]

A study that analyzed the development of molars in hominids and Miocene apes found that a larger “ratio of the areas of [molar 1] and [molar 3]” could correlate to an increase in fruits found in the diet of these species.[25] An increased ratio of the areas of molars was found to have a negative correlation with the amount of “leaves, flowers, and shoots” in the diet, suggesting that species like Ardipithecus, which had a greater ratio of areas of molars, had gradually transitioned to including more fruit in their diet as the size of their molars increased.[25] Many modern primates who lack such dietary features have been shown to occasionally rely on "fall-back foods" of these sorts, implying robust Australopithecines developed post-canine megadontia as they had to more heavily rely on such foods.[25]

Form and Function[edit]


While Post canine megadontia denotes the enlargement of the premolars and molars found in early hominid ancestors, it did not affect the structural organization of the cusps that make up those teeth, and thus, were used similarly to the premolars and molars that modern humans possess today. The premolars and molars of modern hominids and those affected by postcanine megadontia both have two and between four and five cusps respectively.[26][27] The enlargement of the teeth affected by post-canine megadontia, without a difference in the arrangement or number of cusps that compose them, imparted an increased ability for grinding and crushing matter compared to modern day humans. While the form of the teeth themselves is not affected by post-canine megadontia, the ratio of molar teeth volume to total teeth volume is dramatically larger in specimens with post-canine megadontia compared to their modern human counterparts, an adaptation that shows signs of evolutionary convergence when compared to the form and function of the teeth found in many modern herbivores.[28]

Location and form of modern human teeth.


Post-canine megadontia is associated with specific food material properties. This allows for great insight into the diets of early hominins that exhibited the trait. Post-canine megadontia is most commonly linked to diets rich in foods that are “small, chemically sealed, and resistant to bolus formation.”[29] Having these larger teeth in comparison to the oral cavity size breaks down food particles more, which will increase the effectiveness of the natural processes of food processing that occur within the mouth.[29] For example, the large transverse dimensions of corpses of Homo floresiensis from the Liang Bua cave on Flores Island in Indonesia suggest that these early hominids had postcanine megadontia and a diet with great masticatory stress.[30] However, as Homo evolved, the amount of masticatory stress involved in eating decreased as “behavioral adaptations for extraoral food processing” were further developed. Thus, tool making Liang Bua corpses would have a comparatively smaller transverse dimensions of the skull, meaning their “mascilatory functional morphology” deviates greatly from the Pleistocene Homo.[30]'

Skull of a Homo floresiensis next to a modern human skull


Megadontia works by increasing the ratio of minimum to maximum second moments of area or the efficiency of a shape to resist bending or malformation.[31] This resistance is tied to whichever specific axis about which the bending is being applied.[32] Also called mandible robusticity, this characteristic allows for much stronger mastication of food. However, calculations made using biomechanical models does not necessarily perfectly predict the efficiency of different mandibular compositions in resistance to bending forces. Shearing is also an important factor in mastication effectiveness, and resistance to shear is proportional to the cross sectional area of the teeth. In postcanine Megadontia specimens, the cross sectional area is on average much larger than modern hominids which implies greater shear stress resistance.[32]


Some important genes involved in the development and regulation of tooth formation include BMP4, FGF8, and homeobox genes such as MSX1, PAX9, PITX2, SHOX2, Barx1, and Shh to name a few.[33][34] Research suggests that homeobox genes are mainly responsible for much of the variance in tooth morphogenesis observed in fossilized hominids.[33] It is theorized that tooth enlargement is due to several different gene mechanisms, none of them fully understood, and that selection acts on molars and pre-molars as a singular unit rather than on individual teeth.[33]

There are a few theories concerning the selection mechanisms. One theory is that selection acts on the variation in the molars and pre-molars presented by the homeobox genes in hominid species.[33] Another theory suggests that post-canine megadontia resulted from the spatial reassignment by homeobox genes that increased post-canine tooth size while simultaneously decreasing the size of the canines.[33]

For the transition from megadontia to normal-sized post canine teeth and its inverse relationship to brain size, one hypothesis proposes that an inactivation of the MYH16 gene, which resulted in an increase in brain size, decreased temporal muscle mass.[31] The decrease in muscle allowed for the brain to grow, which might have allowed early hominids to develop tools.[31] A second hypothesis suggests that the SRGAP2 gene is responsible instead.[31] The inhibition of this gene allows for an increase in brain development.[31]

Comparative Biology[edit]

Compared with Modern Human Dental Morphology[edit]

Compared to present day humans, early hominids such as Paranthropus aethiopicus and Australopithecus garhi [35] had significantly larger dental morphology in their molars and premolars and smaller incisors. The hominids possessing post-canine megadontia had thick molar enamel, premolars with molarized roots, and lower molars that had additional capsules.[36] Rather than inheriting their early hominid ancestors’ large sized molars, human molars evolved significantly, reducing instead to a size more similar to their front teeth. Contrary to megadont hominins’ dominant second molars, modern humans’ first molar is the largest, and their mandibles can rarely fit a third molar.[37]

Compared to Primates and Other Species[edit]

The morphology of teeth among species offers insight into their diet and phylogeny. The constant chewing in primate’s diets created a selection in primate molar shape, notably possessing cusp tips to ingest seeds.[19] In order to achieve maximum chewing efficiency as the food toughness increases, folivorous primates tend to have larger post-canines than frugivorous primates.[38] In primates, positive allometry exists between the size of post canine teeth in primates and cranial length. This relationship has also been suggested in other groups of mammals, but the differences in postcanine size in primates are less variant compared to other mammals.[39][40] Other species with herbivorous diets have adaptations in their post canines in order to eat plant material,[41] but the term postcanine megadontia typically refers to the dental adaptation in the hominid group.[2]


  1. ^ "Paranthropus aethiopicus". The Smithsonian Institution. Retrieved March 2011.  Check date values in: |access-date= (help)
  2. ^ a b c d McHenry, Henry M. (1984-07-01). "Relative cheek-tooth size in Australopithecus". American Journal of Physical Anthropology. 64 (3): 297–306. ISSN 1096-8644. PMID 6433716. doi:10.1002/ajpa.1330640312. 
  3. ^ "McHenry, H. M. (1984), Relative cheek-tooth size in Australopithecus. Am. J. Phys. Anthropol., 64: 297–306. doi:10.1002/ajpa.1330640312". 
  4. ^ Lacruz, Rodrigo S.; Dean, M. Christopher; Ramirez-Rozzi, Fernando; Bromage, Timothy G. (2008-08-01). "Megadontia, striae periodicity and patterns of enamel secretion in Plio-Pleistocene fossil hominins". Journal of Anatomy. 213 (2): 148–158. ISSN 1469-7580. PMC 2526111Freely accessible. PMID 19172730. doi:10.1111/j.1469-7580.2008.00938.x. 
  5. ^ Delezene, Lucas K.; Zolnierz, Melissa S.; Teaford, Mark F.; Kimbel, William H.; Grine, Frederick E.; Ungar, Peter S. (2013-09-01). "Premolar microwear and tooth use in Australopithecus afarensis". Journal of Human Evolution. 65 (3): 282–293. PMID 23850295. doi:10.1016/j.jhevol.2013.06.001. 
  6. ^ Brown, Peter; Maeda, Tomoko (2009-11-01). "Liang Bua Homo floresiensis mandibles and mandibular teeth: a contribution to the comparative morphology of a new hominin species". Journal of Human Evolution. Paleoanthropological Research at Liang Bua, Flores, Indonesia. 57 (5): 571–596. PMID 19589559. doi:10.1016/j.jhevol.2009.06.002. 
  7. ^ F. Vondra, Carl (1981). Hominid Sites: Their Geologic Settings. Boulder, Colorado: Westview Press, Inc. pp. 165–166. ISBN 0865312621. 
  8. ^ "Ardipithecus ramidus essay | Becoming Human". Institute of Human Origins. February 2009. Retrieved 2016-11-13. 
  9. ^ "Australopithecus africanus essay | Becoming Human". Institute of Human Origins. February 2009. Retrieved 2016-11-13. 
  10. ^ "The Human Lineage Through Time". Institute of Human Origins. February 2009. Retrieved 2016-11-13. 
  11. ^ a b "Paranthropus boisei essay | Becoming Human". Retrieved 2016-11-13. 
  12. ^ "Homo habilis essay | Becoming Human". Retrieved 2016-11-14. 
  13. ^ "Homo floresiensis essay | Becoming Human". Retrieved 2016-11-14. 
  14. ^ "Homo heidelbergensis essay | Becoming Human". Retrieved 2016-11-14. 
  15. ^ "Homo neanderthalensis essay | Becoming Human". Retrieved 2016-11-14. 
  16. ^ a b "Homo sapiens | Becoming Human". Retrieved 2016-11-14. 
  17. ^ a b "" (PDF). doi:10.1371/journal.pone.0023095.pdf.  External link in |title= (help)
  18. ^ a b c d e Jiménez-Arenas, Juan Manuel (30 January 2014). "On the Relationships of Postcanine Tooth Size with Dietary Quality and Brain Volume in Primates: Implications for Hominin Evolution". BioMed Research International. 2014. 
  19. ^ a b Ungar, Peter S. (2007-01-01). Evolution of the Human Diet: The Known, the Unknown, and the Unknowable. Oxford University Press, USA. ISBN 9780195183467. 
  20. ^ Lacruz, Rodrigo S; Dean, M Christopher; Ramirez-Rozzi, Fernando; Bromage, Timothy G (2016-11-13). "Megadontia, striae periodicity and patterns of enamel secretion in Plio-Pleistocene fossil hominins". Journal of Anatomy. 213 (2): 148–158. ISSN 0021-8782. PMC 2526111Freely accessible. PMID 19172730. doi:10.1111/j.1469-7580.2008.00938.x. 
  21. ^ Constantino, Paul; Wood, Bernard (2007-03-01). "The Evolution of Zinjanthropus boisei". Evolutionary Anthropology: Issues, News, and Reviews. 16 (2): 49–62. ISSN 1520-6505. doi:10.1002/evan.20130. 
  22. ^ a b c Jiménez-Arenas, Juan Manuel (2013). "Tooth size and metabolic requirements in Primates: The ‘equivalence between exponents’ under discussion". Int. J. Morphol. 31 (4): 1191–1197. doi:10.4067/s0717-95022013000400008. 
  23. ^ a b Ungar, Peter (2010). Mammal Teeth: Origin, Evolution, and Diversity. Baltimore, Maryland: Johns Hopkins University Press. 
  24. ^ a b Jolly, C (1970). "The seed-eaters: a new model of hominid differentiation based on a baboon analogy". Man. 5 (1): 5–26. doi:10.2307/2798801. 
  25. ^ a b c Teaford; Ungar. "Diet and the evolution of the earliest human ancestors". Proceedings of the National Academy of Sciences of the United States of America. 97 (25): 13506–13511. doi:10.1073/pnas.260368897. 
  26. ^ Weiss, M.L., & Mann, A.E (1985), Human Biology and Behaviour: An anthropological perspective (4th ed.), Boston: Little Brown, pp. 132–135, 198–199, ISBN 0-673-39013-6
  27. ^ yers, P.; Espinosa, R.; Parr, C. S.; Jones, T.; Hammond, G. S.; Dewey, T. A. (2013a). "The Basic Structure of Cheek Teeth". Animal Diversity Web, University of Michigan. Retrieved May 2013.
  28. ^ Reece, J; Meyers, N; Urry, L; Cain, M; Wasserman, S; Minorsky, P; Jackson, R; Cooke, B. Cambell Biology, 9th Edition. Pearson. p. 472. ISBN 9781442531765.
  29. ^ a b Scott, Jeremiah E (December 2012). "Molar size and diet in the Strepsirrhini: Implications for size-adjustment in studies of primate dental adaptation". Journal of Human Evolution. 63 (6): 796–804. PMID 23098627. doi:10.1016/j.jhevol.2012.09.001. Retrieved 7 November 2016. 
  30. ^ a b Daegling, David J.; Patel, Biren A.; Jungers, William L. (1 March 2014). "Geometric properties and comparative biomechanics of Homo floresiensis mandibles". Journal of Human Evolution. 68: 36–46. PMID 24560803. doi:10.1016/j.jhevol.2014.01.001. Retrieved 7 November 2016. 
  31. ^ a b c d e Daegling, D.J.; Grine, F.E. (June 26, 1991). "Compact Bone Distribution and Biomechanics of Early Hominid Mandibles". American Journal of Physical Anthropology. 86: 321–339. PMID 1746641. doi:10.1002/ajpa.1330860302. 
  32. ^ a b Daegling, David (2007). Evolution of the Human Diet. Oxford University. pp. 89–92. ISBN 978-0-19-518347-4. 
  33. ^ a b c d e McCollum, Melanie A.; Sharpe, Paul T. (2001). "Developmental genetics and early hominid craniodental evolution" (PDF). BioEssays. John Wiley & Sons, Inc. 23 (6): 481–493. PMID 11385628. doi:10.1002/bies.1068. 
  34. ^ Lin, Dahe; Huang, Yide; He, Fenglei; Gu, Shuping; Zhang, Guozhong; Chen, YiPing; Zhang, Yanding (2007-05-01). "Expression survey of genes critical for tooth development in the human embryonic tooth germ". Developmental Dynamics. 236 (5): 1307–1312. ISSN 1097-0177. PMID 17394220. doi:10.1002/dvdy.21127. 
  35. ^ Strait, David S.; Grine, Frederick E. (1999-08-20). "Cladistics and Early Hominid Phylogeny". Science. 285 (5431): 1209–1209. ISSN 0036-8075. doi:10.1126/science.285.5431.1209c. 
  36. ^ McCollum, Melanie A. (1999-04-09). "The Robust Australopithecine Face: A Morphogenetic Perspective". Science. 284 (5412): 301–305. ISSN 0036-8075. PMID 10195892. doi:10.1126/science.284.5412.301. 
  37. ^ Emes, Y., Aybar, B., Yalcin, S. (2011). On the Evolution of Human Jaws and Teeth: A Review. Bull Int Assoc Paleodont. 5(1): 37-47.
  38. ^ Lucas, Peter W. (2004-06-03). Dental Functional Morphology: How Teeth Work. Cambridge University Press. ISBN 9780521562362. 
  39. ^ Kanazawa, Eisaku; Rosenberger, A. L. "Interspecific allometry of the mandible, dental arch, and molar area in anthropoid primates: Functional morphology of masticatory components". Primates. 30 (4): 543–560. ISSN 0032-8332. doi:10.1007/BF02380880. 
  40. ^ Swindler, Daris R. (2002-02-21). Primate Dentition: An Introduction to the Teeth of Non-human Primates. Cambridge University Press. ISBN 9781139431507. 
  41. ^ Romer, A. S. (1959). The Vertebrate Story. University of Chicago Press.