A comparison of the position of the mental foramen in Chinese and British mandibles

The antero-posterior position of the mental foramen was studied in 68 Chinese and 44 British skulls of known or calculated age at death. All skulls showed low pre-mortem tooth loss and had a good occlusion. The position of the foramen was related to the body of the mandible as well as to the standing mandibular teeth using two previously published methods. There was no significant difference in the size of the Chinese and British mandibles. There was a significant difference between the two groups when measurements relating the foramen to the body of the mandible (symphysis menti) were considered, the foraminal position being more distal in the Chinese group. The modal position of the foramen in the Chinese sample was along the long axis of the second premolar, whereas in the British sample it lay between the apices of the first and second premolar. The foraminal position apparently moved distally in both groups with age and this was likely to be associated with mesial tooth drift and age-related attrition.     

Ontogenetic migration of the mental foramen in Neandertals and modern humans

Since the nineteenth century, researchers have noted that Neandertal and modern human adults differ in mental foramen position, although the ontogenetic changes in the position of this feature have only recently come under the scrutiny of paleoanthropologists. Research on mental foramen position has focused on whether this feature is inferior to a particular tooth. However, tooth position may not be a reliable indicator of mental foramen position because of variability in tooth size within and between taxa and during eruption events. As opposed to observing the mental foramen with respect to the postcanine teeth, we examined linear distances from the mental foramen to other mandibular landmarks. Modern human adults may appear truncated, or paedomorphic, in mental foramen position with respect to Neandertal adults. However, infants of the two taxa differ substantially in anterior mandibular form. The initial differences in the shape of the mental region may be related to the embryological position of the mental foramen in modern humans and its role in the development of the mental trigone. The shape changes that accrue thereafter, possibly from faster mandibular growth rates in Neandertals, further distinguish the adults from one another. Although mandibular shape differences exist from early infancy onwards, adults of the two taxa are broadly similar in bi-mental foramen breadth with respect to mandibular size. For this reason, qualitative assessments of mental foramen position may provide less taxonomic information than previously thought.     

Measurements of tooth wear among Australian Aborigines: I. Serial loss of the enamel crown

The dental casts made from Aboriginal children during the course of a longitudinal growth study in Central Australia provided material for analyzing tooth wear under known environmental conditions. The wear facets produced on the occlusal surfaces were clearly preserved on the dental stone casts and recorded the progress of enamel attrition from ages 6 to 18. These casts were photographed and traced by electronic planimetric methods that automatically recorded the location and size of wear facets on the first and second permanent molars. These areas of worn tooth surface were compared to the total tooth surface. The worn surface was regressed on age to calculate wear rates of each tooth. Discriminant analyses were also performed to determine the significance of dental attrition differences between the sexes at each age group. The total wear on each tooth was highly correlated with age as expected but females wore their teeth at a significantly higher rate than males. The mandibular molars wore more rapidly than maxillary teeth in both sexes. The discriminant analysis successfully grouped 91% of the cases according to age and sex. Pattern of wear, the location, and size of wear facets also differed between age groups and sex. The questions of why there is a difference between male and female wear or why there is greater wear on one arch or arch region have no ready answers. The differing rates and pattern of dental wear do suggest that arch shape and growth rates may be the answer though it has yet to be tested. However, the occlusal surface wear is useful for age estimation in a population and provides a record of shifting masticatory forces during growth.     

Dentition and tooth replacement pattern in Chalcides (Squamata; Scincidae)

This study was undertaken as a prerequisite to investigations on tooth differentiation in a squamate, the Canarian scincid Chalcides. Our main goal was to determine whether the pattern of tooth replacement, known to be regular in lizards, could be helpful to predict accurately any stage of tooth development. A growth series of 20 laboratory-reared specimens, aged from 0.5 month after birth to about 6 years, was used. The dentition (functional and replacement teeth) was studied from radiographs of jaw quadrants. The number of tooth positions, the tooth number in relation to age and to seasons, and the size of the replacement teeth were recorded. In Chalcides, a single row of pleurodont functional teeth lies at the labial margin of the dentary, premaxillary, and maxillary. Whatever the age of the specimens, 16 tooth positions were recorded, on average, in each quadrant, suggesting that positions are maintained throughout life. Replacement teeth were numerous whatever the age and season, while the number of functional teeth was subject to variation. Symmetry of tooth development was evaluated by comparing teeth two by two from the opposite side in the four jaw quadrants of several specimens. Although the relative size of some replacement teeth fitted perfectly, the symmetry criterion was not reliable to predict the developmental stage of the opposite tooth, whether the pair of teeth compared was left-right or upper-lower. The best fit was found when comparing the size of successive replacement teeth from the front to the back of the jaw. Every replacement tooth that is 40-80% of its definitive size is followed, in the next position on the arcade, by a tooth that is, on average, 20% less developed. Considering teeth in alternate positions (even and odd series), each replacement tooth was a little more developed than the previous, more anterior, one (0.5-20% when the teeth are from 10-40% of their final size). The latter pattern showed that tooth replacement occurred in alternate positions from back to front, forming more or less regular rows (i.e., "Zahnreihen"). In Chalcides, the developmental stage of a replacement tooth in a position p can be accurately predicted provided the developmental stage of the replacement tooth in position p-1 or, to a lesser degree, in position p-2 is known. This finding will be particularly helpful when starting our structural and ultrastructural studies of tooth differentiation in this lizard.     

Relation of the mental foramen to teeth on the mandibles belonging to the Byzantium period

Fifty mandibles belonging to the Byzantium period were studied in order to determine to racial differences about of the localization of the mental foramen according to the mandibular teeth. Mandibles of adult males without missing teeth, proximal decay and proximal attrition were used. On the right side, the most common position of the mental foramen was between the first and second lower teeth (50%), whereas on the left side, the most common position was in line with the longitudinal axis of the lower second premolar tooth (46%). Because of materials including mostly Alpine's and a few of Mediterranean subraces, two different positions of the mental foramen were determined in high similar ratios.     

Geratodontology and horn growth of the impala (Aepyceros melampus)

Examination of the jaws of an impala population showed advanced wear on mandibular M1 compared with other ungulates which have been examined. This could lead to an erroneous interpretation of age if based upon mandibular tooth wear alone. Explanations are offered for this pattern in terms of the apparent pattern of wear of the impala molar teeth. Suggestions are also put forward for a method of determining specific age, from a conceptual wear model, when only extreme parameters are known. Horn growth in the male is also described.     

Intrapopulation variation in macro tooth wear patterns—a case study from Igloolik,Canada

The pattern of human tooth wear—the way it varies between teeth in the mouth—is crucial to our understanding of important questions in archeology and paleoanthropology, such as the contrasts in diet and behavior between Neanderthals and early modern humans in Europe and Asia, or with the adoption of agriculture in the Americas. Little is known, however, about the way in which wear patterns develop with increasing age or the way in which they differ between males and females. One explanation is that few living people show the high rates of tooth wear seen worldwide throughout the preindustrial archaeological record. The study described here investigates the macroscopic pattern of tooth wear in a unique group of known age and sex dental casts from living Canadian Inuit from Igloolik. The results show that the Igloolik people possessed a pattern of extremely heavy anterior tooth wear, relative to the first molar and the other posterior teeth, which is attributed to the use of the anterior teeth in cultural practices as well as the extreme and marginal environments in which they lived. Heavy anterior tooth wear was established at an early age and maintained throughout life; statistically significant differences were found between the wear patterns of males and females and are explained in terms of sexual division of labor within the community. This study highlights the need to understand both intra‐ and interpopulation variation in tooth wear patterns when interpreting patterns in past human groups. Am J Phys Anthropol, 2012. © 2012 Wiley Periodicals, Inc.     

Evidence for a trade-off between early growth and tooth wear in Svalbard reindeer

Ruminants depend on efficient physical degradation of forage through chewing to increase the surface area of the food particles presented to the microflora. Fossil evidence suggests that increased molar height is an adaptation for wear tolerance in dry ecosystems with sparse vegetation, but no study has shown selection pressure for hypsodonty in contemporary ruminants. We explored the relationships between particle size in rumen, tooth wear (scanned molar occlusal topography), age and body mass of female Svalbard reindeer living in an arctic desert at 78 degrees latitude on Svalbard. We predicted that (H1) if the rumen particle size is determined mainly by constraints due to tooth wear, and if tooth wear is mainly a function of age, average particle size in rumen should increase with age. From allometric relations it is known that larger individuals can survive on a lower-quality diet, we therefore predicted (H2) larger particle sizes with increases in (ln) body mass, irrespective of age and wear. Lastly, if there is a trade-off between growth and tooth wear in dry ecosystems (a selection pressure for hypsodonty), we predicted (H3) that teeth of heavier animals should be more worn than those of lighter animals of the same age. The proportion of small particles (<1.0 mm) decreased rapidly with increasing age (consistent with H1). Heavier females within an age class had more worn teeth (consistent with H3) than lighter ones. A close-to-isometric relationship between particle size and body mass suggested that heavier animals partly compensated for reduced tooth efficiency by chewing more. We provide the first evidence of a trade-off between fast early growth and wear (a somatic cost) of a senescence-related trait--the structure and height of the molar--in a wild ruminant inhabiting an arctic desert where selection pressure for increased tooth height is expected. This suggests that foraging conditions are more extreme than the environment in which the species originally evolved.     

Interproximal wear facets and tooth associations in the Paşalar hominoid sample

Interproximal wear facets were examined on hominoid teeth from the middle Miocene site at Pa?alar, Turkey. The aim was to find matches between adjacent premolar and molar teeth from single individuals that were collected in the field as isolated teeth and use them to reconstruct tooth rows. These were then used to investigate: (1) the wear gradient on the molar teeth; (2) the dispersal of teeth from single mandibles and maxillae; (3) the size ratios among the molars; and (4) the number of individuals represented by the hominoid sample. Facets were scored for size and shape and were assessed visually using photographs and superimposed outline drawings on acetate transparencies. Out of a sample of approximately 1,500 teeth collected between 1983 and 1996, 532 molars and 258 premolars produced apparent matches making up 160 tooth rows. These were then examined rigorously for morphological consistency and state of wear, and, employing the criterion that only the most unequivocal associations should be used, the final number was reduced to 48 tooth rows-31 mandibular and 17 maxillary. The tooth associations represent a minimum of 21 individuals and probably as many as 34. Molar wear was rapid, with M1s having almost twice as much wear as M3s, as measured by a wear-gradient index. The M2s are intermediate but generally closer to M1s in degree of wear, as are P4s. This wear pattern suggests either delayed eruption of M3s or extremely abrasive diets causing rapid, heavy wear. There is some indication that the wear patterns in Griphopithecus alpani and Kenyapithecus kizili are different, with the latter perhaps having a lower wear gradient, but the K. kizili sample is very small. In both species, the M2 is the largest molar and the M1 is the smallest. Separation of individual teeth in the 48 tooth associations varied from widely separated-up to 8.5m apart-to within a few centimeters of each other. One tooth row (D922) was found with the teeth in contact but the maxillary bone had dissolved away. Two dispersal mechanisms have been identified from earlier taphonomic work: transport of disarticulated elements to the fossil site and reworking of sediments by spring action.     

Age determination and body growth of the Common duiker Sylvicapra grimmia(Mammalia)

Age determination in the Common duiker Sylvicapra grimmia was investigated by analysis of tooth eruption and replacement sequence, incremental lines of tooth cementum and tooth wear in a unique collection of 48 known-age skulls, and also by analysis by post-natal body growth in known-age duiker. In both the mandible and maxilla, permanent molariform teeth were fully erupted and in wear by 26 months of age. There was little variation in the age of eruption and replacement of all molariform teeth, making this a particularly useful feature of the duiker for age determination purposes. In contrast, the variability in eruption of the incisiforms, coupled with the difficulty in distinguishing deciduous incisiforms from the permanent counterparts, placed an unexpected limitation on the use of these teeth. Although the apparent linear relationship between tooth attrition and age has potential for further investigation as an age determination technique, the cementum annuli were not correlated with chronological age. Theoretical Von Bertalanffy equations were used to analyse body growth with age. It was concluded that because the asymptote of growth was reached at such an early age, and because there is so much individual variation in growth, body growth, including horn growth, is of very limited value for age determination. Female duiker were significantly larger than males.     

Cheek tooth erosion in male babirusa (genus Babyrousa)

The wear on the occlusal surfaces of male babirusa cheek teeth was evaluated in 53 skulls of Babyrousa babyrussa from Buru and the Sula Islands and 87 skulls of B. celebensis from Sulawesi, Indonesia. Based on the comparative lengths of their continually growing maxillary canine teeth, the skulls were divided into five ‘age categories’ (A–E). Numerical and symbolic codes representing tooth wear were applied to each pillar (cusp region) of the mandibular and maxillary permanent third and fourth premolar teeth, and the first, second and third permanent molar teeth. There was no significant difference between the tooth wear patters of skulls in groups A and B, or in groups C and D, and so these were amalgamated. There was close correspondence in wear patterns between each side of the mouth in both species and in each age group. The wear patterns of the mandibular and maxillary teeth, although not identical, were very similar, as were the wear patterns of both species. In group A + B for both species tooth wear was relatively slight, with the M1 teeth experiencing most relative wear. There was almost no wear of the M3 teeth. In group C + D substantial wear of upper and lower M1 was evident. In group E more widespread wear of the cheek teeth was seen, with increased severity of M1 tooth wear, yet there was comparatively much less M2 and M3 tooth wear. The pattern of cheek tooth wear of the Babyrousa spp. was different from that shown by Sus scrofa. Differences in diet selection and processing were highlighted as potential contributing factors. The pattern of cheek tooth wear in male babirusa was not adequate for use to monitor their age.     

广西敢造遗址史前居民口腔的健康状况

广西扶绥敢造遗址是华南新石器时代一处典型的河岸贝丘遗址,其人骨测年结果的上限为8488 BC,下限为6492 BC。本文对敢造遗址2014年出土的108例个体的999枚恒齿进行观察统计,结果显示居民的饮食结构应是以肉食为主并辅以富含淀粉的块茎类植物。该遗址居民的龋齿率高于部分农业人群,但远低于同为华南渔猎—采集经济的鲤鱼墩、甑皮岩和顶蛳山遗址,其原因应与食用块茎类植物的多寡有关。较高的牙结石罹患率(89.86%)可能与鱼类、贝类等高蛋白饮食有关。相比农业、游牧或狩猎人群,该遗址居民偏重的牙齿磨耗可能与食用含沙量较大的螺类、贝类等有关;肉类食物的食用导致该遗址居民上颌前部牙齿磨耗重于后部牙齿,而“上颌前部牙齿舌侧过度磨耗”现象的出现则与食用块茎类植物有关。     

Decelerating and sex-dependent tooth wear in Norwegian red deer

In ungulates, tooth wear is often suggested as a proximate cause of senescence. Tooth wear is expected to be sex-dependent since energetic requirements and food selection varies largely between sexes in sexually dimorphic ungulates. Furthermore, tooth wear may lower mastication efficiency, and we predict a negative correlation between tooth wear and body weight or condition. We tested these predictions on data on tooth wear (estimated as height of first molar) of 1,311 male and 1,348 female red deer ( Cervus elaphus) aged 3-25 years and harvested along the west coast of Norway. The rate of tooth wear decreased with age. Males wear teeth at a higher rate (from 0.61 mm/year in 4-year olds to 0.45 mm/year in 11-year olds) than females (from 0.52 mm/year in 4-year olds to 0.39 mm/year in 11-year olds). Molar height correlated positively with body weight in both sexes, but not after adjusting for body size. Molar height was strongly dependent on body size in 3-year-old individuals (when tooth wear is minimal). Earlier reports in the literature of a positive correlation between tooth height and body weight may therefore be due to initial size differences rather than differences in condition due to tooth wear.     

Tooth wear and compensatory modification of the anterior dentoalveolar complex in humans

In populations living in environments where teeth wear severely, some compensatory modification of the dentoalveolar complex is thought to occur during life whereby functional occlusion is maintained as tooth substance is lost by wear. This study investigates one aspect of this modification process: Changes in the anterior dentoalveolar complex that are accompanied with wear were examined in a series of Japanese skeletal samples. In the prehistoric Japanese hunter-gatherer population heavy wear occurs over the entire dentition. The following changes were demonstrated to have occurred in the anterior segment of the dentition accompanied by wear on the anterior teeth: The anterior teeth tip lingually with wear up to a nearly upright position to fill in interproximal spaces that would have been generated by wear, and to maintain contact relations between adjacent teeth. At the same time, the anterior surface of the maxillary alveolar process also inclines lingually to a certain extent. The amount of lingual tipping is greater in the maxillary anterior teeth than in their mandibular antagonists. It is because of this discrepancy that, with age, the horizontal component of the overlap between maxillary and mandibular anterior teeth decreases, and their bite form changes from scissor bite to edge-to-edge bite. Lesser degrees of lingual tipping of the anterior teeth were also detected in the prehistoric agriculturists and historic Japanese populations. The variation in the degree of lingual tipping observed among the samples is explained by inter-population variation in severity and pattern of tooth wear. This and other evidence suggests that mechanisms that compensate for wear in the anterior dentition may be characteristic of all living human populations, independently of the degree of wear severity endured in their environments.     

Sex-specific strategies of dentine depletion in red deer

Worn teeth in herbivore ungulates may be related to lower efficiency in mastication and hence lower performance. However, selection should favour maximal performance in terms of body mass and reproductive capacity during reproductive lifespan, when permanent teeth are already partially worn. We hypothesize that wear rate may respond to a strategy of use of tooth materials (notably dentine), which balances instantaneous wear rate and performance against tooth preservation for future performance and reproduction. In the present study, we investigated 4151 carcasses of Iberian red deer Cervus elaphus hispanicus and show that more worn molars were not related to lower performance throughout age. By comparing between sexes, tooth wear rates were smaller in females than in males, but the relationship between tooth wear and body performance also differed between the sexes: females did not show a significant relationship between tooth wear and performance but males with more worn teeth were in general heavier and had larger antlers until senile age, when more depleted teeth were related to smaller antlers. These results reveal, for the first time, sex-specific lifetime strategies of dentine expenditure: maintenance of performance ability throughout a longer reproductive lifespan in females, compared with maximizing current performance by depleting dentine reserves within a shorter lifespan in males.  © 2008 The Linnean Society of London, Biological Journal of the Linnean Society , 2008, 93 , 487–497.     

Dental identification and age determination in Elephas maximus

The dentition of an elephant (fossil or extant) can yield clues to the animal's age species identity, provided the teeth are correctly identified. Identifying the serial category of elephant teeth is difficult because the size, shape and position of each tooth changes throughout life, as the teeth form, erupt, wear and move throught the jaw. In the present study, teeth from over 100 museum specimens of the Asian elephant ( Elephas maximus ) were the basis for establishing size ranges for cheek teeth in six serial categories (designated by Roman numerals I to VI). Although the teeth vary greatly and overlap in their dimensions, reliable identifications (as well as estimates of an individual's age in years) can be obtained using three or more measurements. An appreciation for dental variability in Elephas maximus will demand a re-evaluastion of frequently-cited examples of macroevolutionary patterns within the Elephantidae.     

Relation of dental wear to the concentrations of essential minerals in teeth of the California sea lion <Emphasis Type="Italic">Zalophus Californianus Californianus</Emphasis>

Tooth wear in marine mammals has been attributed to age, feeding habits, behavior, and contaminants. Advanced tooth wear in some California sea lions, including some of very young age (<5 yr), in the Gulf of California, suggests that there are variations in chemical composition of tooth parts, wherein the concentrations of certain trace minerals might be anomalous, making them more susceptible to erosion. The concentrations of the essential minerals Ca, P, K, Na, Fe, Mg, and Zn in the dentition of Zalophus c. californianus are documented for the first time and are compared for sea lion teeth with different degrees of wear. Canine teeth and molars from 45 skulls collected at 15 localities since 1978 were digested in perchloric acid and analyzed using atomic adsorption spectrometry, the results being expressed in milligrams per 100 g. An index of tooth wear (Id) was established, involving the average wear on the teeth and the age of the organism. No significant difference was detected in the variables, but there was one between ages (p=0.02). A higher degree of wear was observed up to 7 yr of age than from this age onward. Mineral concentrations did not explain the excessive wear observed (correlation, p>0.09; ANOVA, p>0.15); however, the Ca concentration of the teeth was inversely proportional to the age of the animal (sexes combined, p=0.026) and particularly significant for the females (r ²=0.112, r=−0.335, p=0.039). Females could be more prone to decalcification because of their annual bone investment in their offspring. Animals of both sexes were susceptible to tooth wear as their age increased, but the higher frequency of animals between 4 and 7 yr suggests an impact on survival at early stages probably linked to deficient feeding and chronic malnutrition.     

Variation in dental wear and tooth loss among known‐aged,older ring‐tailed lemurs (Lemur catta): a comparison between wild and captive individuals

Tooth wear is generally an age‐related phenomenon, often assumed to occur at similar rates within populations of primates and other mammals, and has been suggested as a correlate of reduced offspring survival among wild lemurs. Few long‐term wild studies have combined detailed study of primate behavior and ecology with dental analyses. Here, we present data on dental wear and tooth loss in older (>10 years old) wild and captive ring‐tailed lemurs (Lemur catta). Among older ring‐tailed lemurs at the Beza Mahafaly Special Reserve (BMSR), Madagascar (n=6), the percentage of severe dental wear and tooth loss ranges from 6 to 50%. Among these six individuals, the oldest (19 years old) exhibits the second lowest frequency of tooth loss (14%). The majority of captive lemurs at the Indianapolis Zoo (n=7) are older than the oldest BMSR lemur, yet display significantly less overall tooth wear for 19 of 36 tooth positions, with only two individuals exhibiting antemortem tooth loss. Among the captive lemurs, only one lemur (a nearly 29 year old male) has lost more than one tooth. This individual is only missing anterior teeth, in contrast to lemurs at BMSR, where the majority of lost teeth are postcanine teeth associated with processing specific fallback foods. Postcanine teeth also show significantly more overall wear at BMSR than in the captive sample. At BMSR, degree of severe wear and tooth loss varies in same aged, older individuals, likely reflecting differences in microhabitat, and thus the availability and use of different foods. This pattern becomes apparent before “old age,” as seen in individuals as young as 7 years. Among the four “older” female lemurs at BMSR, severe wear and/or tooth loss do not predict offspring survival. Am. J. Primatol. 72:1026–1037, 2010. © 2010 Wiley‐Liss, Inc.     

Brief communication: interproximal tooth wear: a new observation.

Microscopic observations were made of wear on the proximal surfaces of tooth crowns of Australian Aboriginals and whites. Typical wear facets displayed well-defined borders within which vertical or near vertical furrows, ranging from about 0.1 to 0.5 mm in width, were noted. Furrows on the interproximal surface of one tooth seemed to "interdigitate" with those on the proximal surface of the adjacent tooth. These observations are not consistent with the commonly-held view that interproximal tooth wear results from a buccolingual movement of adjacent teeth that maintain contact through mesial migration. Vertical or near vertical movement of teeth, possibly including a tipping action, must be an important factor, although the precise nature of the movement requires further investigation.     

Determination of relative age in the dugong Dugong dugon (Müller) from a study of skulls and teeth

The dugong is a rare animal and virtually nothing is known of the time scale of its life cycle. A collection of 41 skulls and lower jaws, all from the north-eastern coastal region of Australia, was studied with the primary aim of relative age determination. It was found that they fell naturally into three groups corresponding roughly with skull size, according to number of incisors, number and state of eruption of cheek teeth and position of the cheek teeth in the jaw. These groups were arbitrarily termed adults, adolescents and juveniles. Skull measurements and state of fusion of skull sutures upheld these life stage groups, and to some extent helped to subdivide them. Further subdivision into a relative age sequence was achieved by "state of succession of cheek teeth" groups, and an index of size for the last cheek tooth. Sexual dimorphism is also discussed.