Behavioral inferences from the high levels of dental chipping in Homo naledi http://researchonline.ljmu.ac.uk/6367/ Article LJMU has developed LJMU Research Online for users to access the research output of the University more effectively.
Objectives A tooth chip occurs when a hard object forcefully contacts the surface of the tooth, typically removing enamel from the occlusal edge. In this study, chipping patterns in extant primates were compared, and hard‐object‐feeding assessed alongside other factors (e.g., grit mastication and dental properties), to elucidate dietary and behavioral inferences in archeological and paleontological samples. Materials and methods Thirteen species of extant primates were studied, including eight species within the Cercopithecidae, two within the Ceboidea, and three within the Hominoidea. Four additional species were also incorporated from the literature for some of the analyses. The severity (Grade 1–3), position (buccal, lingual, mesial, and distal) and number of tooth fractures were recorded for each specimen. Results Species considered hard‐object‐feeding specialists presented higher rates of chipping, with sakis, mandrills, sooty mangabeys and Raffles' banded langurs having high chipping rates (28.3%, 36.7%, 48.4%, and 34.7% of teeth, respectively). Species that seasonally eat harder foods had intermediate chipping frequencies (e.g., brown woolly monkeys: 18.5%), and those that less commonly consume hard food items had the lowest chipping frequencies (e.g., Kloss gibbon: 7.3%; chimpanzees: 4.4%). Discussion The results suggest hard food mastication influences differences in chipping prevalence among the species studied. Although Homo fossil samples show high rates of chipping comparable to hard‐object‐feeding extant primates, they display a different pattern of chipping, supporting the hypothesis that these fractures are mostly non‐food related (e.g., grit mastication in Homo naledi; non‐masticatory tooth use in Neanderthals).
Dental caries has been reported in a variety of primates, although it is still considered rare in wild populations. In this study, 11 catarrhine primate taxa (n = 339 individuals; 7946 teeth) were studied for the presence of caries. A differential diagnosis of lesions in interproximal regions of anterior teeth was undertaken, since they had been previously described as both carious and non‐carious in origin. Each permanent tooth was examined macroscopically, with severity and position of lesions recorded. Two specimens were examined further, using micro‐CT scans to assess demineralization. Differential diagnosis confirmed the cariogenic nature of interproximal cavities on anterior teeth (ICATs). Overall results show 3.3% of all teeth (i.e., anterior and posterior teeth combined) were carious (n = 262), with prevalence varying among species from 0% to >7% of teeth affected. Those with the highest prevalence of ICATs include Pan troglodytes verus (9.8% of anterior teeth), Gorilla gorilla gorilla (2.6%), Cercopithecus denti (22.4%), Presbytis femoralis (19.5%), and Cercopithecus mitis (18.3%). ICATs make up 87.9% of carious lesions on anterior teeth. These results likely reflect dietary and food processing differences among species, but also between the sexes (e.g., 9.3% of all female P. troglodytes verus teeth were carious vs. 1.8% in males). Processing cariogenic fruits and seeds with the anterior dentition (e.g., wadging) likely contributes to ICAT formation. Further research is needed in living primate populations to ascertain behavioral/dietary influences on caries occurrence. Given the presence of ICATs in frugivorous primates, their diagnosis in archaeological and paleontological specimens may shed light on diet and food processing behaviors in fossil primates.
Enamel hypoplasia is often split into several macroscopic categories, including pit, localised, linear and plane-form defects. All types have been considered a sign of 'non-specific stress' during dental development in archaeological, as well as palaeoanthropological and other samples. There is growing evidence suggesting many defects may not be caused by illness or malnutrition during childhood, instead relating to trauma to the developing tooth, genetic conditions or specific environmental factors, i.e., may not be associated with 'stress' to the individual. In this study all types of macroscopic enamel hypoplasia were recorded, including pitting, linear, plane and localised type defects, in three extant primate species and three fossil hominin species. The aim is to compare the characteristics and prevalence of different types of enamel hypoplasia among species and discuss potential differences in aetiology. The results show that samples have diverse prevalences of different kinds of defects, and pitting, linear and localised defects likely have different aetiologies. Additionally, dental characteristics (e.g., tooth morphology, developmental timing/speed and enamel structure) heavily influence the likelihood of specific types of enamel hypoplasia forming. In sum, studies that include only one type of enamel hypoplasia, or focus on one tooth type, to generate a 'stress' rating for a sample may miss relevant information when comparing groups. Instead, it may be beneficial to record different types of defects separately, for all teeth, and then consider how genetic, environmental and tooth property factors may influence population differences.
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