Skip to main content

Advertisement

Log in

Bony outgrowths on the jaws of an extinct sperm whale support macroraptorial feeding in several stem physeteroids

  • Short Communication
  • Published:
Naturwissenschaften Aims and scope Submit manuscript

Abstract

Several extinct sperm whales (stem Physeteroidea) were recently proposed to differ markedly in their feeding ecology from the suction-feeding modern sperm whales Kogia and Physeter. Based on cranial, mandibular, and dental morphology, these Miocene forms were tentatively identified as macroraptorial feeders, able to consume proportionally large prey using their massive teeth and robust jaws. However, until now, no corroborating evidence for the use of teeth during predation was available. We report on a new specimen of the stem physeteroid Acrophyseter, from the late middle to early late Miocene of Peru, displaying unusual bony outgrowths along some of the upper alveoli. Considering their position and outer shape, these are identified as buccal maxillary exostoses. More developed along posterior teeth and in tight contact with the high portion of the dental root outside the bony alveoli, the exostoses are hypothesized to have developed during powerful bites; they may have worked as buttresses, strengthening the teeth when facing intense occlusal forces. These buccal exostoses further support a raptorial feeding technique for Acrophyseter and, indirectly, for other extinct sperm whales with a similar oral apparatus (Brygmophyseter, Livyatan, Zygophyseter). With a wide size range, these Miocene stem physeteroids were major marine macropredators, occupying ecological niches nowadays mostly taken by killer whales.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2

References

  • Bhusari P, Kumathalli KI, Raja S, Mishra AK (2011) Bony exostosis following a traumatic blow: a case report. J Indian Dent Assoc 5:285–287

    Google Scholar 

  • Bianucci G, Landini W (2006) Killer sperm whale: a new basal physeteroid (Mammalia, Cetacea) from the Late Miocene of Italy. Zool J Linnean Soc 148:103–131. doi:10.1111/j.1096-3642.2006.00228.x

    Article  Google Scholar 

  • Bloodworth B, Marshall CD (2005) Feeding kinematics of Kogia and Tursiops (Odontoceti: Cetacea): characterization of suction and ram feeding. J Exp Biol 208:3721–3730. doi:10.1242/jeb.01807

    Article  PubMed  Google Scholar 

  • Cankaya AB, Erdem MA, Isler SC et al (2012) Oral and maxillofacial considerations in Gardner's Syndrome. Int J Med Sci 9:137–141. doi:10.7150/ijms.3989

    Article  PubMed Central  PubMed  Google Scholar 

  • Fahlke JM (2012) Bite marks revisited—evidence for middle-to-late Eocene Basilosaurus isis predation on Dorudon atrox (both Cetacea, Basilosauridae). Palaeontol Electron 15(32A):1–16

    Google Scholar 

  • Fonseca LC, Kodama NK, Nunes FCF et al (2007) Radiographic assessment of Gardner's syndrome. Dentomaxillofac Radiol 36:121–124. doi:10.1259/dmfr/18554322

    Article  CAS  PubMed  Google Scholar 

  • Fordyce RE (1994) Waipatia maerewhenua, new genus and new species (Waipatiidae, new family), an archaic late Oligocene dolphin from New Zealand. Proc San Diego Soc Nat Hist 29:147–178

    Google Scholar 

  • Horning GM, Cohen ME, Neils TA (2000) Buccal alveolar exostoses: prevalence, characteristics, and evidence for buttressing bone formation. J Periodontol 71:1032–1042. doi:10.1902/jop.2000.71.6.1032

    Article  CAS  PubMed  Google Scholar 

  • Lambert O, Bianucci G, de Muizon C (2008) A new stem-sperm whale (Cetacea, Odontoceti, Physeteroidea) from the latest Miocene of Peru. C R Palevol 7:361–369. doi:10.1016/j.crpv.2008.06.002

    Article  Google Scholar 

  • Lambert O, Bianucci G, Post K et al (2010) The giant bite of a new raptorial sperm whale from the Miocene epoch of Peru. Nature 466:105–108. doi:10.1038/nature09067

    Article  CAS  PubMed  Google Scholar 

  • Miles AEW, Grigson C (1990) Colyer's variations and diseases of the teeth of animals, revisedth edn. Cambridge University Press, Cambridge

    Book  Google Scholar 

  • de Muizon C (1988) Les vertébrés fossiles de la Formation Pisco (Pérou). Troisième partie: Les Odontocètes (Cetacea, Mammalia) du Miocène. Trav Inst Fr Etudes Andines 42:1–244

    Google Scholar 

  • Pechenkina EA, Benfer RA Jr (2002) The role of occlusal stress and gingival infection in the formation of exostoses on mandible and maxilla from Neolithic China. J Comp Hum Biol 53:112–130. doi:10.1078/0018-442X-00040

    Article  CAS  Google Scholar 

  • Sathya K, Kanneppady SK, Arishiya T (2012) Prevalence and clinical characteristics of oral tori among outpatients in Northern Malaysia. J Oral Biol Craniofac Res 2:15–19. doi:10.1016/S2212-4268(12)60005-0

    Article  Google Scholar 

  • Sawair FA, Shayyab MH, Al-Rabab'ah MA, Saku T (2009) Prevalence and clinical characteristics of tori and jaw exostoses in a teaching hospital in Jordan. Saudi Med J 30:1557–1562

    PubMed  Google Scholar 

  • Schandorff S (1997) Developmental stability and skull lesions in the harbour seal (Phoca vitulina) in the 19th and 20th centuries. Ann Zool Fenn 34:151–166

    Google Scholar 

  • Seagars DJ (1982) Jaw structure and functional mechanics of six delphinids (Cetacea, Odontoceti). Dissertation, San Diego State University

  • Turnbull WD (1970) Mammalian masticatory apparatus. Fieldiana Geol 18(2):1–209

    Google Scholar 

  • Uhen MD (2004) Form, function, and anatomy of Dorudon atrox (Mammalia, Cetacea): an archaeocete from the middle to late Eocene of Egypt. Univ Michigan Pap Paleontol 34:1–222

    Google Scholar 

  • Verstraete F, Van Aarde R, Nieuwoudt B, Mauer E, Kass P (1996) The dental pathology of feral cats on Marion Island, part II: periodontitis, external odontoclastic resorption lesions and mandibular thickening. J Comp Pathol 115:283–297. doi:10.1016/S0021-9975(96)80085-5

    Article  CAS  PubMed  Google Scholar 

  • Werth AJ (2004) Functional morphology of the sperm whale tongue, with reference to suction feeding. Aquat Mamm 30:405–418

    Article  Google Scholar 

  • Westneat MW (2004) Evolution of levers and linkages in the feeding mechanisms of fishes. Integr Comp Biol 44:378–389. doi:10.1093/icb/44.5.378

    Article  PubMed  Google Scholar 

Download references

Acknowledgments

We thank W Aguirre, E Díaz, R Salas-Gismondi, and M Urbina for giving us access to the specimen and for its final preparation. Constructive comments from C de Muizon, ND Pyenson, and two anonymous reviewers considerably enhanced the quality of the article. This work was financially supported by MIUR grant (PRIN 2012YJSBM, resp. GB), SYNTHESYS grant (BE-TAF-2842, GB), and Return Grant of the Belgian Federal Science Policy Office (2012–April 2013, OL).

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Olivier Lambert.

Additional information

Communicated by: Sven Thatje

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Lambert, O., Bianucci, G. & Beatty, B.L. Bony outgrowths on the jaws of an extinct sperm whale support macroraptorial feeding in several stem physeteroids. Naturwissenschaften 101, 517–521 (2014). https://doi.org/10.1007/s00114-014-1182-2

Download citation

  • Received:

  • Revised:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s00114-014-1182-2

Keywords

Navigation