The dentition of fallow deer (Dama dama): a scoring scheme to assess age from wear of the permanent molariform teeth

The sequence of tooth wear was determined from skulls of fallow deer of known age. A system for scoring molariform tooth wear has been devised so that small but readily recognizable wear changes of the individual cusps may be recorded and used to assess the age of animals of unknown birth dates. The technique can be readily adapted for other ruminant species with the appropriate database.     

Some stages in the early development of the post-incisor dentition of Trichosurus vulpecula (Phalangeroidea: Marsupialia)

The present paper reports observations from serial sections of five pouch-young specimens on the early stages of tooth ontogeny in the post-incisor dentition of Trichosurus vulpecula. The order of cusp development and calcification for the molariform teeth is recorded and closely resembles that of placentals. Some features concerning the development of the replacing premolar are noted and compared with the conditions observed in Setonix brachyurus , another marsupial. A number of non-functional cheek teeth are reported.     

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.     

Development and size of the teeth of Macaca mulatta.

A cross-sectional sample of 151 skulls from Macaca mulatta of known age and similar rearing in U.S. Primate Centers was analyzed to determine age-related "norms" of stages of development and size of teeth. The stages of development from the follicle of a deciduous incisor in the fetus to completion of the root with apex closed of the permanent third molar were related to age. The age range observed for eruption of each tooth was noted and related to its stage of development. The crown of each erupted tooth was found to be completely developed, but growth of its root continued for a longer, indeterminate period. When a deciduous tooth was exfoliated, the crown of the permanent successor was found to be completed and root growth had begun. Measurements of both mesiodistal and faciolingual diameters and of crown length of the teeth in situ and of total length and root length on roentgenograms were examined for sexual dimorphism. The faciolingual diameter of the deciduous mandibular second incisor and of both second molars showed the greatest sexual dimorphism among both diameters of all deciduous teeth. The mesiodistal and faciolingual diameters of the mandibular premolars were found to be the best dimensions in discriminant functions for identifying sex in the absence of permanent canines.     

Increasing human tooth length between birth and 5.4 years

Most previous studies of tooth development have used fractional stages of tooth formation to construct growth standards suitable for aging juvenile skeletal material. A simple alternative for determining dental age is to measure tooth length throughout development. In this study, data on tooth length development are presented from 63 individuals of known age at death, between birth and 5.4 years, from an archeological population recovered from the crypt of Christ Church, Spitalfields, London. Isolated developing teeth (304 deciduous, 269 permanent) were measured in millimeters and plotted against individual age. Regression equations to estimate age from a given tooth length, are presented for each deciduous maxillary and mandibular tooth type and for permanent maxillary and mandibular incisors, canines, and first permanent molars. Data on the earliest age of root completion of deciduous teeth and initial mineralization and crown completion of some permanent teeth in this sample are given, as well as the average crown height and total tooth length from a small number of unworn teeth. This method provides an easy, quantitative and objective measure of dental formation appropriate for use by archeologists and anthropologists. © 1993 Wiley-Liss, Inc.     

Feeding specialization in Herichthys minckleyi: a trophically polymorphic fish

Diet specialization in the trophically polymorphic cichlid fish Herichthys minckleyi was examined using gut contents. Individual H. minckleyi were categorized as having molariform, papilliform or undetermined pharyngeal jaws. The presence of enlarged flattened pharyngeal jaw teeth was used to categorize H. minckleyi as molariform, and the possession of only small pencil‐like pharyngeal teeth was used to classify fish as papilliform. Undetermined individuals (<50 mm standard length, L _S) were not assigned to one of the two larger morphotypes. Arthropods were found to be generally rare in H. minckleyi gut contents, but when present, they were most frequently recovered from undetermined individuals. The percentage of plant material consumed by undetermined H. minckleyi was not as great as papilliforms ingested on average, and snail crushing by undetermined H. minckleyi was not evident. A significantly greater mean percentage of plant detritus was recovered from papilliforms compared to molariforms. Snails were crushed by molariforms more frequently than by papilliforms. When only molariforms and papilliforms that had crushed snails were compared, a greater number of snails were crushed by molariforms. No relationship was found between molariform L _S and the number of snails crushed, but greater molariform tooth number, adjusted for L _S, was indicative of recent snail crushing. The maintenance of H. minckleyi pharyngeal jaw variation could be promoted by intraspecific diet differentiation.     

The dentition of red deer (Cervus elaphus): a scoring scheme to assess age from wear of the permanent molariform teeth

Skulls of red deer ( Cervus elaphus of known age were examined. A scoring procedure devised for fallow deer ( Dama dama ) was used to relate tooth wear to a particular age (Brown & Chapman, 1990). The precise sequential nature of tooth wear as it appeared on the slopes and tips of cusps, on the marginal ridges and links between cusps was recorded. From these data a base has been provided from which estimates of age may be made of animals of unknown age. The variability for the scores are given for 95% prediction intervals from the regression of age on total molar wear score.     

Relationships between age and dental attrition in Australian aboriginals

Tooth wear scores (ratios of exposed dentin to total crown area) were calculated from dental casts of Australian Aboriginal subjects of known age from three populations. Linear regression equations relating attrition scores to age were derived. The slope of the regression line reflects the rate of tooth wear, and the intercept is related to the timing of first exposure of dentin. Differences in morphology between anterior and posterior teeth are reflected in a linear relationship between attrition scores and age for anterior teeth but a logarithmic relationship for posterior teeth. Correlations between age and attrition range from less than 0.40 for third molars (where differences in the eruption and occlusion of the teeth resulted in different patterns of wear) to greater than 0.80 for the premolars and first molars. Because of the generally high correlations between age and attrition, it is possible to estimate age from the extent of tooth wear with confidence limits of the order of +/- 10 years.     

Age assessment in infant crab-eating monkeys (Macaca fascicularis) based on tooth development

Tooth development was studied in 13 Macaca fascicularis monkeys with known dates of birth. Regular intra-oral examination was carried out and standardized lateral radiographs were collected from 27 until 150 weeks of age under general anaesthesia.
Three stages of tooth development were determined radiographically: onset of crypt formation, onset of mineralization, and crown completion. A fourth stage, the emergence, was determined clinically. Developmental stages were recorded for six mandibular and five maxillary teeth.
The ages of emergence of the permanent teeth and the developmental stages of the third molars showed the largest variation. A significant sex difference with earlier maturation in males was found for the start of crypt formation of the maxillary permanent canines and the maxillary second premolars, and for the start of mineralization of the maxillary permanent canines.
The data provide a tool by which chronological age can be assessed of Macaca fascicularis monkeys between 30 and 80 weeks of age. Owing to an interphase of about one year without significant developmental features in the dentition, age assessment based on tooth development cannot be performed from about 80 to 130 weeks of age. Age assessments are possible for the period between 130 and 150 weeks of age. However, in this period the reliability of the data is lower due to larger time intervals and standard deviations.     

Foregut morphology and ontogeny of the spider crab Maja brachydactyla (Brachyura,Majoidea, Majidae)

We describe the morphology of the foregut of the spider crab Maja brachydactyla Balss, 1922, from first larval stage to adult, with detailed stage‐specific documentation using light and scanning electron microscopy. A total of 40 ossicles have been identified in the foregut of adults of M. brachydactyla using Alizarin‐Red staining. The morphological pattern of the ossicles and gastric mill is very similar to other Majoidea species with only a few variations. The foregut of the zoeae stages appeared as a small and simple cavity, with a cardio‐pyloric valve that separates the stomach into cardiac and pyloric regions. The pyloric filter is present from the first zoea, in contrast to the brachyuran species which have an extended larval development. Calcified structures have been identified in the cardio‐pyloric valve and pyloric region of the zoeal stages. The most significant changes in foregut morphology take place after the metamorphosis from ZII to megalopa, including the occurrence of the gastric mill. In the megalopa stage, the foregut ossicles are recognizable by their organization and general morphology, but are different from the adult phase in shape and number. Moreover, the gastric teeth show important differences: the cusps of the lateral teeth are sharp (no molariform); the dorsal tooth have a small, dentate cusp (not a well‐developed quadrangular cusp); and the accessory teeth are composed of one sharp peak (instead of four sharp peaks). The gastric mill ontogeny from megalopa to adult reveals intermediate morphologies during the earlier juvenile stages. The relationship between gastric mill structures with food preferences and their contribution to the brachyuran phylogeny are briefly discussed. J. Morphol. 276:1109–1122, 2015. © 2015 Wiley Periodicals, Inc.     

Estimating the distribution of probable age-at-death from dental remains of immature human fossils

In two historic longitudinal growth studies, Moorrees et al. (Am J Phys Anthropol 21 (1963) 99-108; J Dent Res 42 (1963) 1490-1502) presented the "mean attainment age" for stages of tooth development for 10 permanent tooth types and three deciduous tooth types. These findings were presented graphically to assess the rate of tooth formation in living children and to age immature skeletal remains. Despite being widely cited, these graphical data are difficult to implement because there are no accompanying numerical values for the parameters underlying the growth data. This analysis generates numerical parameters from the data reported by Moorrees et al. by digitizing 358 points from these tooth formation graphs using DataThief III, version 1.5. Following the original methods, the digitized points for each age transition were conception-corrected and converted to the logarithmic scale to determine a median attainment age for each dental formation stage. These values are subsequently used to estimate age-at-death distributions for immature individuals using a single tooth or multiple teeth, including estimates for 41 immature early modern humans and 25 immature Neandertals. Within-tooth variance is calculated for each age estimate based on a single tooth, and a between-tooth component of variance is calculated for age estimates based on two or more teeth to account for the increase in precision that comes from using additional teeth. Finally, we calculate the relative probability of observing a particular dental formation sequence given known-age reference information and demonstrate its value in estimating age for immature fossil specimens.     

Age estimation of the White rhinoceros (Ceratotherium simum)

Age estimation criteria for the southern White rhinoceros ( Ceratotherium simum simum ) are presented both for free-ranging live animals and for cranial material. These are based on: (i) size appearance and horn development of live animals; (ii) stages of tooth eruption; (iii) tooth wear classes; (iv) attrition in height of the first molar tooth; (v) counts of cementum lines visible in tooth sections. Selected measurements are presented for live animals, skulls and horns.
For live animals, eight size classes are distinguished, seven of these covering immature animals up to ten years of age. Sixteen tooth wear classes are established, based on eruption and surface wear of maxillary dentition. Chronological ages were assigned from individually known animals followed in the field, and from skulls from animals for which exact records of age were available, or which could be assigned to an age category from appearance at death. Cementum line counts corresponded approximately with age in years, despite difficulties in interpreting lines. Some variability was observed, possibly related to nutritional conditions.
The maximum cementum line count obtained indicates a longevity of at least 40 years. Full body weight and socio-sexual maturity are attained by males between 10 and 15 years of age, while females first give birth between six and eight years of age. Sequences and times of tooth eruption are similar to those reported for the Black rhinoceros ( Diceros bicornis ).
Comparative cranial and body measurements are presented for the northern subspecies ( Ceratotherium simum cottoni ).     

Malnutrition Has No Effect on the Timing of Human Tooth Formation

The effect of nutrition on the timing of human tooth formation is poorly understood. Delays and advancements in dental maturation have all been reported as well as no effect. We investigated the effect of severe malnutrition on the timing of human tooth formation in a large representative sample of North Sudanese children. The sample (1102 males, 1013 females) consisted of stratified randomly selected healthy individuals in Khartoum, Sudan, aged 2-22 years using a cross-sectional design following the STROBE statement. Nutritional status was defined using WHO criteria of height and weight. Body mass index Z-scores and height for age Z-scores of ≤−2 (cut-off) were used to identify the malnourished group (N = 474) while the normal was defined by Z-scores of ≥0 (N = 799). Clinical and radiographic examination of individuals, with known ages of birth was performed including height and weight measurements. Mandibular left permanent teeth were assessed using eight crown and seven root established tooth formation stages. Mean age at entry and mean age within tooth stages were calculated for each available tooth stage in each group and compared using a t-test. Results show the mean age at entry and mean age within tooth stages were not significantly different between groups affected by severe malnutrition and normal children (p>0.05). This remarkable finding was evident across the span of dental development. We demonstrate that there is little measurable effect of sustained malnutrition on the average timing of tooth formation. This noteworthy finding supports the notion that teeth have substantial biological stability and are insulated from extreme nutritional conditions compared to other maturing body systems.     

Ecological and evolutionary consequences of the trophic polymorphism in Cichlasoma citrinellum (Pisces: Cichlidae)

The neotropical cichlid fish Cichlasoma citrinellum is polymorphic in the structure of its pharyngeal jaw apparatus and external morphology. The pharyngeal jaws are either gracile and bear slender, pointed teeth (papilliform) or robust with strong, rounded teeth (molariform). Molariform morphs have a ‘benthic’, and papilliform morphs a ‘limnetic’ body form. Furthermore, this species is also polychromatic, with yellow and black morphs. The molariform morphology of the pharyngeal jaw apparatus adapts the fish for cracking and feeding on snails. Based on analysis of stomach contents, 94% of the molariform morph ate snails whereas only 19%, of the papilliform morph did so. This result suggests that the morphs occupy different ecological niches. The morphology of the pharyngeal jaw apparatus does not correlate significantly with sex, but it does with body colouration (P<0.005). Cichlasoma citrinellum mate assortatively with their own colour; therefore a mating preference for colour may lead to genetic isolation of trophic morphs. The frequency of the molariform morph differs strikingly among populations of five Nicaraguan lakes and its abundance is correlated with the abundance of snails, the fishes' principal prey item. Among populations the frequency of molariform morphs decreases in the dry season. Morphology possibly changes reversibly within particular individuals between seasons. These results suggest that phenotypic plasticity and polymorphisms may be an adaptive characteristic of cichlid fishes. Patterns of intraspecific morphological variation match patterns of interspecific morphological diversification which suggests that universal developmental mechanisms canalize the possible expressions of morphology. The ability to respond morphologically to environmental shifts, in conjunction with genetically determined trophic polymorphisms and sexual selection via mate choice, could be the basis for speciation through intermediate stages of polymorphism of the impressive adaptive radiation of cichlid fishes.     

Osteology and morphology of the characiform fish Alestes stuhlmanniiPfeffer, 1896(Alestidae) from the Rufiji River basin,East Africa

The osteology of a population of the characiform fish Alestes stuhlmannii, from the Rufiji River basin of Tanzania, is described, and meristic and morphometric data from over 100 specimens, ranging from 15·5 to 218 mm standard length are given. Two allometric changes occur during growth of this fish: both the number of gill rakers and the interorbital width relative to the head length increase with size. There are also changes in tooth form associated with growth in A. stuhlmannii, with the unicuspid teeth of juveniles becoming almost molariform in adults. This change in dentition with age, and therefore size, may have implications for recognizing taxa, some of which (the fossil genera Sindacharax and Bunocharax, and the living dwarf petersiines) have been distinguished by jaw or dental characters.     

Tooth morphology of Notosuchus terrestris (Notosuchia: Mesoeucrocodylia): New evidence and implications

Notosuchia is a large and diverse group of Crocodyliforms, characterized, among other features, by a heterodont dentition. New information on the tooth anatomy of Notosuchus terrestris is presented, based on well-preserved specimens from the Late Cretaceous of Patagonia (southern Argentina). This allows a complete characterization of its dental anatomy (composed by incisiviform, caniniform, and molariform teeth) that includes autapomorphic features and derived features shared with Sphagesaurus and Mariliasuchus. This includes the extensive wear facets in molariforms, indicative of tooth–tooth occlusion and a sharp keel that bears rounded denticles. Notosuchus also shares with Mariliasuchus the presence of a tooth with a transitional morphology located at the premaxilla–maxilla contact and the absence of interalveolar septa in the entire premaxillary and maxillary dentition.     

Variation in crown and root formation and eruption of human deciduous teeth

The aim of this study was to document variation of deciduous tooth formation and eruption. The material comprises 121 individuals of known or estimated age (using tooth length) from Spitalfields in London, and radiographs of 61 healthy living children aged 2-5 years. Other skeletal material from two medieval Scottish archaeological sites (Whithorn, N=74; Newark Bay, N=59) was also examined. Stages of crown and root formation as well as eruption (alveolar, midway, and occlusal levels) were assessed for each developing maxillary and mandibular tooth from radiographs or direct vision. Age of attainment for individual stages was calculated by probit analysis, and these data were also adapted for use in estimating age. The timing of crown completion was similar to previously reported studies, but apex completion times were later. Analysis of data relative to the first and second molars at the two stages D (crown complete) and F (root length > or =crown height) allowed comparison with the Scottish material. No significant differences were observed between population groups for tooth formation or eruption. These data fill several gaps in the literature, and will be useful in assessing maturity and predicting age during early childhood.     

Age estimation of the roe deer (Capreolus capreolus) mandibles from the Mesolithic site of Star Carr, Yorkshire, based on radiographs of mandibular tooth development

A scheme developed by Brown & Chapman, (1991a), which allocates scores to stages of tooth development from radiographs, has been applied to 12 of the 28 roe deer ( Capreolus capreolus ) mandibular rami recovered from the early Mesolithic site of Star Carr, N. Yorkshire ( c. 7500 BC). The mandibles of 35 known-age roe deer kids from Britain and Denmark were also radiographed. The developmental stages of all premolars and molars were analysed and assigned a score using the scheme. After radiographing, four of the Star Carr rami could be paired with a fair degree of confidence, reducing the sample size from 12 to 10 roe deer. Comparisons of scores between the archaeological and modem populations revealed that seven of the Star Carr mandibular rami are aged approximately 10 to 11 months. The youngest is nine months, and the oldest 12 months. These results have significant implications for determining the seasonal presence of humans at the site. Contrary to the received view of a purely late spring/summer occupation of the site, it is now apparent that Star Carr was also visited during the late winter and early spring.     

Tooth and consequences: Heterodonty and dental replacement in piranhas and pacus (Serrasalmidae)

Tooth replacement in piranhas is unusual: all teeth on one side of the head are lost as a unit, then replaced simultaneously. We used histology and microCT to examine tooth‐replacement modes across carnivorous piranhas and their herbivorous pacu cousins (Serrasalmidae) and then mapped replacement patterns onto a molecular phylogeny. Pacu teeth develop and are replaced in a manner like piranhas. For serrasalmids, unilateral tooth replacement is not an “all or nothing” phenomenon; we demonstrate that both sides of the jaws have developing tooth rows within them, albeit with one side more mineralized than the other. All serrasalmids (except one) share unilateral tooth replacement, so this is not an adaptation for carnivory. All serrasalmids have interlocking teeth; piranhas interdigitate lateral tooth cusps with adjacent teeth, forming a singular saw‐like blade, whereas lateral cusps in pacus clasp together. For serrasalmids to have an interlocking dentition, their teeth need to develop and erupt at the same time. We propose that interlocking mechanisms prevent tooth loss and ensure continued functionality of the feeding apparatus. Serrasalmid dentitions are ubiquitously heterodont, having incisiform and molariform dentitions reminiscent of mammals. Finally, we propose that simultaneous tooth replacement be considered as a synapomorphy for the family.     

Relative dental maturity and associated skeletal maturity in prehistoric native Americans of the Ohio valley area

Estimation of age-at-death of subadults in prehistoric skeletal samples based on modern reference standards rests on a number of assumptions of which many are untestable. If these assumptions are not met error of unknown magnitude and direction will be introduced to the subadult age estimates. This situation suggests that an independent estimate or estimates of age-related features, free of most of the assumptions made when using modern reference standards may be useful supplements in evaluating the age of subadults in prehistoric samples. The present study provides an internally consistent, population-specific measure of maturity for prehistoric Ohio valley Native Americans based on the seriation of dental development that may be used as a supplement to age-estimation. The developing dentition of 581 subadults from eight Ohio valley prehistoric-protohistoric groups was seriated within and among individuals resulting in a sequence of tooth development and a sequence of individuals from least to most mature. Dental maturity stages or sorting categories were then defined based on exclusive, easily observable, and highly repeatable tooth-formation stages. Tooth eruption (into occlusion), bone lengths, and fusion of skeletal elements are summarized by dental maturity stage. This procedure provides maturity estimates for skeletal features ordered by dental maturity stages derived from the same sample thus making explicit the relationship between dental and skeletal maturity.