Dentition and age determination of the giraffe Giraffa camelopardalis

Thirteen tooth eruption stages and their corresponding chronological ages are descri bed from a series of giraffe jaws. These can be used for age determination in giraffes with immature dentition. Significant correlations of the lingual crown height ( r =0-957; P < 0001) and lingual occlusal surface width ( r =0-959; P < 0001) with the number of dark staining incremental lines in the cementum of thin decalcified sections of the maxillary first molar were found. The regression equations derived from these relationships provide a further method for determining the age of a giraffe. A composite plate showing maxillary first molar wear patterns provides a means of roughly assigning an age to a particular specimen. Thin sections of undecalcified teeth, mandible measurements, various other indices of tooth wear and eye lens mass were investigated and found unsuitable for age determination in this     

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.     

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.     

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.     

Field age determination of leopards by tooth wear

Age determination is an important tool in wildlife studies. Estimating the age of animals in the field using tooth wear criteria may be subject to error as a result of variations between individuals, habitats and populations. Data on age estimation of leopards and tooth wear characteristics are lacking. Nineteen leopards in Namibia were assessed for tooth eruption and wear. Between 1991 and 1995 leopards (including 13 individuals of known age) were monitored at one year intervals ('28 leopard years') to record age and tooth wear. At the age of two years leopards had fully developed dentition. Wear started with the incisors and canines, and spread to the premolars and molars. A chronology of tooth eruption and wear in relation to age is presented. Above the age of three years, male leopards showed higher frequencies of enamel flaking and canine fractures than females.     

Age determination in roe deer — a new approach to tooth wear evaluated on known age in dividuals

A novel, simple, and objective method is presented for ageing roe deerCapreolus capreolus (Linnaeus, 1758) evaluated on 471 lower jaws from roe deer of known age (351 with permanent premolars). It is based on tooth eruption patterns and presence/absence of wear characters in jaws from roe deer integrated in a scoring system. Permanent cheek teeth emerge in May–July in the year af ter birth, which enables precise age determination of individuals with deciduous premolars. For individuals with permanent cheek teeth, the method provides the correct age for all individ uals younger than 13 months and > 80% of all individuals between 13 and 24 months old. For older in dividuals the accuracy decreases, but decent accuracy is achieved to the age of 48 months. Males have higher wear rates than females corroborating recent documentation of sex-specific life history tactics in ungulates. The data originate from two separated Danish roe deer populations exposed to contrasting habitats, but no difference in wear rate is found between populations. Thus, previous concern about the validity of age determination methods based on tooth wear may have been overstated. The findings demonstrate that objective measures of tooth wear can provide the basis for age determination in ungulate species that are otherwise difficult to age.     

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.     

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 criteria and life expectancy of Roe deer (Capreolus capreolus) in coniferous forest in North-eastern England

In a comparative study of ageing techniques on 101 Roe deer from Hamsterley Forest, County Durham, it was found that cementum layering in the incisor was completely reliable and that in the molar slightly less so. Estimates of age from cusp wear and general attrition of the dentition were highly correlated with those from layering. The rate of tooth wear was high. The dry weight of the eye lens was of little value as an index of age. The annual static mortality of both sexes was apparently close to 30% throughout most of the life span, and the form of the life table similar to that of female Roe deer in Thetford Chase, East Anglia, and on the Kala estate in Denmark. The oldest individuals obtained were aged 9½ years.     

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 ).     

Dental fast track: Prenatal enamel growth,incisor eruption,and weaning in human infants

Correlation between the timing of permanent first molar eruption and weaning age in extant primates has provided a way to infer a life history event in fossil species, but recent debate has questioned whether the same link is present in human infants. Deciduous incisors erupt at an age when breast milk can be supplemented with additional foods (mixed feeding), and weaning is typically complete before permanent first molars erupt. Here, I use histological methods to calculate the prenatal rate by which enamel increases in thickness and height on human deciduous incisors, canines, and molars (n = 125). Growth trajectories for each tooth type are related to the trimesters and assessed against the eruption sequence and final crown height. Analyses show that central incisors initiate early in the second trimester with significantly faster secretion rates relative to canines and second molars, which initiate closer to birth. Even though initial extension rates were correlated with crown height and scaled with positive allometry within each tooth class, the relatively short incisors still increased in height at a significantly faster rate than the taller canines and molars. The incisor prenatal “fast track” produces a greater proportion of the crown before birth than all other tooth types. This growth mechanism likely facilitates early incisor eruption at a time when the mixed feeding of infants can be initiated as part of the weaning process. Findings provide a basis from which to explore new links between developmental trends along the tooth row and mixed feeding age in other primates. Am J Phys Anthropol 156:407–421, 2015. © 2014 Wiley Periodicals, Inc.     

Bigger teeth for longer life? Longevity and molar height in two roe deer populations

The role of tooth wear as a proximate cause of senescence in ruminants has recently been highlighted. There are two competing hypotheses to explain variation in tooth height and wear; the diet-quality hypothesis predicting increased wear in low-quality habitats, and the life-history hypothesis predicting molar height to be related to expected longevity. We compared tooth height and wear from roe deer of known age from two contrasting populations of roe deer (Capreolus capreolus) in France: Trois Fontaines (TF) with good habitat and shorter animal life expectancy and Chizé (CH) with poor habitat and longer animal life expectancy. There was no population difference in tooth wear, leading to rejection of the diet-quality hypothesis. However, despite their smaller body size, initial molar height for animals from CH was larger than for animals from TF. This provides the first evidence that variation in longevity between populations can lead to differences in molar height within a species.     

Effects of age, sex and density on body weight of Norwegian red deer: evidence of density-dependent senescence

There are only a few recent studies that have demonstrated senescence in ungulates and nothing is known regarding how patterns of senescence may vary as a function of density Senescence in general is linked to the cost of reproduction, which probably increases with density in ungulates and may differ between the sexes. Further, senescence in ungulates is also regarded to be a function of tooth wear rates. As density dependence and sexual differences in food choice have been well documented, this may lead to different tooth wear rates and, thus, possibly density-dependent and sex-specific patterns of senescence. We therefore investigated the effects of age, sex, density and their possible interactions on the variability of body weight in 29,047 red deer harvested during 1965-1998 from Norway, out of which 380 males and 1452 females were eight years or older. There was clear evidence that spatio-temporal variation in density correlated negatively with body weights. In addition, there was evidence of senescence in both male and female red deer. Age at onset of senescence in females was after 20 years of age and independent of population density. In males, the onset and rate of senescence increased with increasing population density. The onset of senescence for males was at ca. 12 years of age at low density, but decreased to approximately ten years of age at high density. The pattern of density-dependent senescence in males, but not that in females, can be explained if (i) the cost of reproduction increases with density more strongly in male than in female red deer, and/or (ii) tooth wear rates are density dependent in males, but not in females. We discuss the ability of these two different, not mutually exclusive hypotheses in explaining the observed pattern of senescence.     

Tooth eruption in Reeves' muntjac (Muntiacus reevesi) and its use as a method of age estimation (Mammalia: Cervidae)

The sequence of tooth eruption and replacement in Reeves' muntjac was determined from captive animals of known age. Pronounced sexual dimorphism is shown by the permanent upper canine which in the male is large, tusk-like and is used as a weapon. The upper canine was the first deciduous tooth to be replaced in males, at approximately 21 weeks of age, compared with 53–57 weeks in the female. The permanent mandibular teeth erupted in the order: molars, first and second incisors, premolars, third incisor and canine. The maxillary teeth erupted in the order: first molar, canine (in male), second and third molars, canine (in female), premolars. The full complement of 34 functional permanent teeth was attained by 83–92 weeks of age.     

The use of tooth eruption and wear, body weight and antler characteristics in the age estimation of male wild and park Fallow deer (Dama dama)

The eruption and wear of the cheek teeth of male Fallow deer from a park and wild population has been studied for age determination purposes. It was found possible to age accurately up to 48 months animals whose date of death was known, whether they were from a wild or park population. It was found that up to at least this age individual and environmental differences affecting animals born in successive years did not mask those resulting fromthe restricted seasonal breeding of this species.
Antler development and body weight were studied in relation to the ages obtained and were found to be of limited value for age estimation.     

Age determination of the African buffalo, Syncerus caffer Sparrman

Age criteria for the African buffalo are described. These are based on the tooth eruption sequence and on wear of the first molar. Assignment of absolute ages to the tooth eruption and wear classes has been made by reference to known-age animals and to numbers of cementum lines in tooth sections. For ageing animals to the nearest year, the normal degree of accuracy of the methods is assumed to be about ± 1/2year (1–5 years of age); about ± 1 year (5–15 years of age); and about ±2 years (15-20years of age). A field method of age determination is presented based on horn characteristics and relative body size.     

桂林甑皮岩新石器时代遗址2例儿童的年龄问题

作者报告２例于桂林甑皮岩新石器时代早期遗址出土的正处于换牙期的儿童乳、恒牙更换及其被磨耗的状况,讨论了从他们的牙磨耗级估计的年龄与从其乳、恒牙更换关系估计的年龄的误差,并提出用现代人牙磨耗级估计史前人类年龄的意见．     

Age determination and growth in the hyrax Procavia capensis (Mammalia: Procaviidae)

The use of eye lens weight, tooth eruption and tooth attrition has been investigated as a method for age determination in the hyrax. Illustrations are presented on the stages of eruption to reduce subjectivity of eruption criteria and to aid age determination. All teeth are fully erupted and in wear by five years of age, from which point age determination can be based on attrition of M3. Growth with age is described by means of the von Bertalanffy equation. Asymptotic weight is reached by 60 months, asymptotic body length and body girth by 40 months, and hindfoot length by 35 months. The asymptotes and the coefficient of catabolism (K) are compared with values obtained in other studies.     

The relative age structure and body masses of complete wild-captured colonies of two social mole-rats, the common mole-rat, Cryptomys hottentotus hottentotus and the Damaraland mole-rat, Cryptomys damarensis

The relative ages of individuals in a complete wild-captured colony of 13 Cryptomys hottentotus hottentotus and a complete wild-captured colony of 25 Cryptomys damarensis were determined by means of tooth wear and eruption patterns and through the degree of ossification of their skeletons.
From sequential tooth wear and eruption patterns four relative age classes were discerned in C. h. hottentotus and five in C. damarensis . These relative age class allocations were supported by the studies on the ossification of the skeletons.
In C. damarensis , older animals are not necessarily the larger-sized individuals. In C. h. hottentotus , however, older animals are usually the larger-sized individuals. The reproductive pair in each of the Cryptomys species are the oldest or amongst the oldest individuals in the colony.
Individuals in a second colony of C. damarensis kept under laboratory conditions for three years maintained greatly disparate body masses which were correlated with the role of the individual within the colony and not, where it was known, with the age of the animal.
An analysis of 13 body and skull measurements performed on a complete colony of 13 C. h. hottentotus and a complete colony of 25 C damarensis revealed that only C. damarensis showed sexual dimorphism. This dimorphism was apparent from an early age but became more pronounced in older animals.     

Mineralization and wear of mandibular first molars in red deer (Cervus elaphus) of known age

The degree of dental wear was measured in 41 mandibular first molars from red deer of known age (range 2–18 years). The calculated wear indices were positively correlated with age ( r = 0.780, P < 0.001). In the same sample, significant ( P < 0.001) differences in hardness (determined by microhardness testing) were observed between enamel and coronal dentine as well as between outer and inner enamel and dentine, respectively. In animals belonging to the same age group (three-year-olds, n = 11), a negative correlation ( r = -0.830, P = 0.0016) was found between wear index and maximum mean enamel hardness. In a sample of five specimens from this age group, a negative correlation ( r = -0.918, P = 0.028) between maximum calcium concentration of enamel (measured by electron microprobing) and wear index was also recorded. We concluded that the intensity of enamel mineralization had a decisive effect on the degree of dental wear. Measuring of enamel hardness and subsequent modification of wear scores or indices is therefore recommended for future studies on the relationship between age and the degree of dental attrition in deer.