Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2011 Dec 22;278(1725):3654-61.
doi: 10.1098/rspb.2011.0528. Epub 2011 Apr 27.

The Hadropithecus conundrum reconsidered, with implications for interpreting diet in fossil hominins

Affiliations

The Hadropithecus conundrum reconsidered, with implications for interpreting diet in fossil hominins

Elizabeth R Dumont et al. Proc Biol Sci. .

Abstract

The fossil 'monkey lemur' Hadropithecus stenognathus has long excited palaeontologists because its skull bears an astonishing resemblance to those of robust australopiths, an enigmatic side branch of the human family tree. Multiple lines of evidence point to the likelihood that these australopiths ate at least some 'hard', stress-limited food items, but conflicting data from H. stenognathus pose a conundrum. While its hominin-like craniofacial architecture is suggestive of an ability to generate high bite forces, details of its tooth structure suggest that it was not well equipped to withstand the forces imposed by cracking hard objects. Here, we use three-dimensional digital reconstructions and finite-element analysis to test the hard-object processing hypothesis. We show that Archaeolemur sp. cf. A. edwardsi, a longer-faced close relative of H. stenognathus that lacked hominin convergences, was probably capable of breaking apart large, stress-limited food items, while Hadropithecus was better suited to processing small, displacement-limited (tougher but more compliant) foods. Our suggestion that H. stenognathus was not a hard-object feeder has bearing on the interpretation of hominin cranial architecture; the features shared by H. stenognathus and robust australopiths do not necessarily reflect adaptations for hard-object processing.

PubMed Disclaimer

Figures

Figure 1.
Figure 1.
Dorsal views of the skulls of (a) H. stenognathus (Vienna cranium NHMW 1934 IV 1) and (b) Paranthropus boisei (KNM-ER 406). Both species have been interpreted as hard-object feeders, although contradictory signals exist for each [6,8,9,12,13].
Figure 2.
Figure 2.
Estimated jaw positions at maximum gape and muscle attachment areas for (a) H. stenognathus and (b) A. sp. cf. A. edwardsi. (Additional details of muscle attachments are provided in the electronic supplementary material, figures S1 and S2.)
Figure 3.
Figure 3.
The predicted distribution of von Mises stress in models of (a,b) A. sp. cf. A. edwardsi and (c,d) H. stenognathus during P4 biting at maximum gape. These models were scaled to predicted body size. Histograms illustrate the distribution of stress across the volume of each model. White areas indicate stresses that exceed the maximum value depicted in the stress histogram (10 MPa). These differences persisted but were smaller in magnitude when the models were scaled to equal body size and when equal ratios of applied force to total surface area were used in order to remove the effects of size on the stress results [34].
Figure 4.
Figure 4.
The predicted distribution of von Mises stress in models of (a,b) A. sp. cf. A. edwardsi and (c,d) H. stenognathus during M2 biting at maximum gape. These models were scaled to predicted body size. Histograms illustrate the distribution of stress across the volume of each model. White areas indicate stresses that exceed the maximum value depicted in the stress histogram (10 MPa). These differences persisted but were smaller in magnitude when the models were scaled to equal body size and when equal ratios of applied force to total surface area were used in order to remove the effects of size on the stress results [34].

References

    1. Constantino P. J., Lee J. J.-W., Chai H., Zipfel B., Ziscovici C., Lawn B. R., Lucas P. W. 2010. Tooth chipping can reveal the diet and bit forces of fossil hominins. Biol. Lett. 6, 826–82910.1098/rsbl.2010.0304 (doi:10.1098/rsbl.2010.0304) - DOI - DOI - PMC - PubMed
    1. Lee-Thorp J. A., Sponheimer M., Passey B. H., Ruiter D. J., Cerling T. E. 2010. Stable isotopes in fossil hominin tooth enamel suggest a fundamental dietary shift in the Pliocene. Phil. Trans. R. Soc. B 365, 3389–339610.1098/rstb.2010.0059 (doi:10.1098/rstb.2010.0059) - DOI - DOI - PMC - PubMed
    1. Dominy N. J., Vogel E. R., Yeakel J. D., Constantino P., Lucas P. W. 2008. Mechanical properties of plant underground storage organs and implications for dietary models of early hominins. Evol. Biol. 35, 159–17510.1007/s11692-008-9026-7 (doi:10.1007/s11692-008-9026-7) - DOI - DOI
    1. Lucas P., Constantino P., Wood B., Lawn B. 2008. Dental enamel as a dietary indicator in mammals. Bioessays 30, 374–38510.1002/bies.20729 (doi:10.1002/bies.20729) - DOI - DOI - PubMed
    1. Kay R. F. 1981. The nut-crackers—a new theory of the adaptations of the Ramapithecinae. Am. J. Phys. Anthropol. 55, 141–15110.1002/ajpa.1330550202 (doi:10.1002/ajpa.1330550202) - DOI - DOI

Publication types