Testing Dietary Hypotheses of East African Hominines Using Buccal Dental Microwear Data - PubMed
- ️Fri Jan 01 2016
Testing Dietary Hypotheses of East African Hominines Using Buccal Dental Microwear Data
Laura Mónica Martínez et al. PLoS One. 2016.
Abstract
There is much debate on the dietary adaptations of the robust hominin lineages during the Pliocene-Pleistocene transition. It has been argued that the shift from C3 to C4 ecosystems in Africa was the main factor responsible for the robust dental and facial anatomical adaptations of Paranthropus taxa, which might be indicative of the consumption of fibrous, abrasive plant foods in open environments. However, occlusal dental microwear data fail to provide evidence of such dietary adaptations and are not consistent with isotopic evidence that supports greater C4 food intake for the robust clades than for the gracile australopithecines. We provide evidence from buccal dental microwear data that supports softer dietary habits than expected for P. aethiopicus and P. boisei based both on masticatory apomorphies and isotopic analyses. On one hand, striation densities on the buccal enamel surfaces of paranthropines teeth are low, resembling those of H. habilis and clearly differing from those observed on H. ergaster, which display higher scratch densities indicative of the consumption of a wide assortment of highly abrasive foodstuffs. Buccal dental microwear patterns are consistent with those previously described for occlusal enamel surfaces, suggesting that Paranthropus consumed much softer diets than previously presumed and thus calling into question a strict interpretation of isotopic evidence. On the other hand, the significantly high buccal scratch densities observed in the H. ergaster specimens are not consistent with a highly specialized, mostly carnivorous diet; instead, they support the consumption of a wide range of highly abrasive food items.
Conflict of interest statement
The authors have declared that no competing interests exist.
Figures

(a) LP4 OH-65 with patina layers covering the microwear features. (b) LM1 KNM-ER-1171 with perykimata—growth lines—and enamel prisms caused by chemical erosion. (c) RP4 OH-5 with post-mortem physical abrasion caused by rolling over sediments. Scale line is 200 μm.

(a) LP4 OH-69 Homo habilis. (b) RM1 KNM-WT-15000 Homo ergaster. (c) LM1 Peninj Paranthropus boisei. Scale line is 200 μm.

The whiskers show the minimum and maximum values (excluding outliers). The box includes the 25–75 percentiles. Both the median values (lines within the boxes) and means (yellow dots) are shown for the total striation density (NT) and length (XT) by species (sample sizes are indicated in brackets). For the outliers the specimen reference numbers are shown.

Plot of the first two discriminant functions (DF1 x axis, DF2 y axis), derived from the microwear variables (ranked data) for the hominines samples studied (Paranthropus aethiopicus brown, Paranthropus boisei beige, Homo habilis cyan, Homo ergaster red), that explain 93,8% of the total variance (55.9% and 37.9%, respectively). The ellipses show one standard deviation of the sample means (68% confidence interval of the sample). The blue lines represent the loadings of the microwear variables on the discriminant functions. The analysis was made with PAS v. 3.

Plot of the first two discriminant functions (DF1 x axis, DF2 y axis), derived from the microwear variables (ranked data) for all the specimens studied and the comparative collections, that explain 73,66% of the total variance (57,25% and 16,41%, respectively). The circles represent the 95% confidence intervals of the group centroids assuming equality of covariance matrices (the size of the circle depend on the sample sizes). The red lines indicate the correlations between the variables considered and the two functions shown. The analysis was made with XLSTAT v. 2015.

The dissimilarities among groups were measured using Fisher's distance derived from the Linear Discriminant Analysis of all the microwear variables (ranked data) for all groups considered. The diagonal dissimilarity matrix was used to derive a hierarchical cluster analysis using an unweighted average agglomeration method in XLSTAT v. 2015.
Similar articles
-
Pérez-Pérez A, Espurz V, Bermúdez de Castro JM, de Lumley MA, Turbón D. Pérez-Pérez A, et al. J Hum Evol. 2003 Apr;44(4):497-513. doi: 10.1016/s0047-2484(03)00030-7. J Hum Evol. 2003. PMID: 12727465
-
Galbany J, Moyà-Solà S, Pérez-Pérez A. Galbany J, et al. Folia Primatol (Basel). 2005 Nov-Dec;76(6):325-41. doi: 10.1159/000089531. Folia Primatol (Basel). 2005. PMID: 16401909
-
Buccal dental microwear texture and catarrhine diets.
Aliaga-Martínez A, Romero A, Galbany J, Hernández-Aguilar RA, Pérez-Pérez A. Aliaga-Martínez A, et al. Am J Phys Anthropol. 2017 Jul;163(3):462-473. doi: 10.1002/ajpa.23219. Epub 2017 Mar 28. Am J Phys Anthropol. 2017. PMID: 28369731
-
Dental evidence for the diets of Plio-Pleistocene hominins.
Ungar PS. Ungar PS. Am J Phys Anthropol. 2011;146 Suppl 53:47-62. doi: 10.1002/ajpa.21610. Am J Phys Anthropol. 2011. PMID: 22101687 Review.
-
Tooth form and function: insights into adaptation through the analysis of dental microwear.
Ungar PS. Ungar PS. Front Oral Biol. 2009;13:38-43. doi: 10.1159/000242388. Epub 2009 Sep 21. Front Oral Biol. 2009. PMID: 19828967 Review.
Cited by
-
Percher AM, Romero A, Galbany J, Nsi Akoue G, Pérez-Pérez A, Charpentier MJE. Percher AM, et al. PLoS One. 2017 Oct 26;12(10):e0186870. doi: 10.1371/journal.pone.0186870. eCollection 2017. PLoS One. 2017. PMID: 29073184 Free PMC article.
-
DeSantis LRG, Sharp AC, Schubert BW, Colbert MW, Wallace SC, Grine FE. DeSantis LRG, et al. Sci Rep. 2020 Jun 1;10(1):8809. doi: 10.1038/s41598-020-65586-w. Sci Rep. 2020. PMID: 32483196 Free PMC article.
References
-
- Bamford MK, Stanistreet IG, Stollhofen H, Albert RM. Late pliocene grassland from Olduvai Gorge, Tanzania. Palaeogeogr Palaeoclimatol Palaeoecol. 2008;257: 280–293.
-
- Behrensmeyer A, Todd N, Potts R, McBrinn G. Late pliocene faunal turnover in the turkana basin, Kenya and Ethiopia. Science. 1997;278: 1589–1594. - PubMed
-
- Bobe R, Behrensmeyer AK. The expansion of grassland ecosystems in Africa in relation to mammalian evolution and the origin of the genus Homo. Palaeogeogr Palaeoclimatol Palaeoecol. 2004;207: 399–420.
-
- Cerling TE. Development of grasslands and savannas in East Africa during the neogene. Palaeogeogr Palaeoclimatol Palaeoecol. 1992;97: 241–247.
MeSH terms
Grants and funding
This research was funded by the Spanish "Ministerio de Ciencia e Innovación" (http://www.idi.mineco.gob.es/portal/site/MICINN/), grant numbers CGL2011-22999 and CGL2014-52611-C2-1-P, both to APP. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
LinkOut - more resources
Full Text Sources
Other Literature Sources
Miscellaneous