Morphological evidence for the biological role of caniniform teeth in combtooth blennies (Blenniidae, Teleostei)

Combtooth blennies have recurved, fang-like caniniform teeth at the rear end of a single row of incisiform teeth. The lengths and positions of these canines were measured in the lower jaws of males of 14 species of Mediterranean Blenniidae. In four species, lower jaw canines were measured in males and females, while in one species, the upper jaw canines of both sexes were also measured. Relative (to body length) canine length in males tends to be significantly greater (10–40%) than in females. There are significant interspecific differences in relative canine length, with smaller species tending to have relatively larger teeth. No significant correlation was obtained between canine length and importance of animal prey in the diet, nor with 'hole fit' of males, which may be related with the intensity of paternal care. We suggest that canines in combtooth blennies are predominately used for predator deterrence and agonistic interactions.     

Allometric relations of teeth and jaws in man

Static adult intraspecific allometry of jaws and teeth was investigated in a sample of 100 Negro crania. The relations between tooth area, postcanine surface, incisor surface, and four viscerocranial measures were examined separately for males and females. Our results indicate a marked lack of morphological integration between P-sets within the orofacial subregion and a similar lack of correspondence between jaw size and tooth size. Allometric analyses indicate that mandibular length scales negatively allometric to maxilloalveolar length and to bigonial width, that canine base area scales positively to upper and lower jaw length, and that all the other teeth scale negatively to jaw length. The postcanine surface area was found to be negatively allometric to the canine base area, which in turn scaled isometrically to incisor surface. Hence, any lengthening of the mandible will tend to be associated with a relative shortening of the maxilla, with relatively larger canines and a relative reduction of the cheek teeth.     

Canine size, shape, and bending strength in primates and carnivores

Anthropoid primates are well known for their highly sexually dimorphic canine teeth, with males possessing canines that are up to 400% taller than those of females. Primate canine dimorphism has been extensively documented, with a consensus that large male primate canines serve as weapons for intrasexual competition, and some evidence that large female canines in some species may likewise function as weapons. However, apart from speculation that very tall male canines may be relatively weak and that seed predators have strong canines, the functional significance of primate canine shape has not been explored. Because carnivore canine shape and size are associated with killing style, this group provides a useful comparative baseline for primates. We evaluate primate maxillary canine tooth size, shape and relative bending strength against body size, skull size, and behavioral and demographic measures of male competition and sexual selection, and compare them to those of carnivores. We demonstrate that, relative to skull length and body mass, primate male canines are on average as large as or larger than those of similar sized carnivores. The range of primate female canine sizes embraces that of carnivores. Male and female primate canines are generally as strong as or stronger than those of carnivores. Although we find that seed-eating primates have relatively strong canines, we find no clear relationship between male primate canine strength and demographic or behavioral estimates of male competition or sexual selection, in spite of a strong relationship between these measures and canine crown height. This suggests either that most primate canines are selected to be very strong regardless of variation in behavior, or that primate canine shape is inherently strong enough to accommodate changes in crown height without compromising canine function.     

Static intraspecific allometry of jaws and teeth in Cercopithecus aethiops

Adult static intraspecific allometry of jaw size and tooth area was evaluated in a sample of 100 Cercopithecus aethiops crania (50 male, 50 female). Tooth areas were calculated from mesiodistal and buccolingual measurements of all the teeth in both arcades and were scaled to four viscero-cranial measurements: bimaxillary breadth, maxillo-alveolar length, mandibular length and bigonial width. Allometric coefficients calculated for jaw dimensions alone indicate tighter viscerocranial integration in females than in males. A finding of note was that half of the variation in maxillo-alveolar length may be accounted for by variation in mandibular length: females are isometric, males negatively allometric.
A similar degree of allometric mosaicism was found when maxillary incisor size was scaled to maxillary length and width. In females, the relationship was negatively allometric, whilst incisor size in males was found to be unrelated to either. Negative allometry characterized the relationship of canine base area to jaw length in both sexes, with males additionally being positively allometric to mandibular width.
The scaling of postcanine tooth areas to jaw length was characterized by a dichotomous pattern: males showed significant mandibular integration whilst females showed only significant maxillary integration. Compensatory tooth size interaction between maxillary canine base area and the summed incisor and postcanine areas was suggested by the significant negative allometric relation between them.     

Interspecific and intraspecific relationships between tooth size and jaw size in primates

The association between mandibular robusticity, postcanine megadontia, and canine reduction in hominins has led to speculation that large and robust jaws might be required to spatially accommodate large canine and molar teeth in hominins and other primates. If so, then variations in mandibular form that are generally regarded as biomechanical adaptations to masticatory demands might instead be incidental effects of functional requirements of tooth support. While the association between large teeth and deep, robust jaws in hominins is well known, the relationship between tooth size and jaw size has not been systematically evaluated in a comparative sample of primates. We evaluate the relationships between molar tooth size, canine tooth size, and mandibular corpus and symphyseal dimensions in a sample of adult anthropoids in interspecific (n=84 species) and intraspecific (n=36 species) contexts. For intraspecific comparisons, tooth size and jaw size are correlated, but for a majority of species this is a function of sexual size dimorphism. Interspecific comparisons lend little direct support to the hypothesis that jaw breadth directly covaries with molar tooth breadth, but they do support the hypothesis that mandibular depth is associated with canine tooth size in males. The latter observation suggests that if there is a causal association between canine size and mandibular depth, it is subject to a threshold effect. In contrast, neither corpus nor symphyseal robusticity, measured as a shape index of breadth/height, are correlated with tooth size. Our results suggest that further studies of the relationship between tooth size and corpus morphology should focus on tooth root size and corpus bony architecture, and that species-specific factors should have a strong impact on such relationships.     

Canine tooth size variability in primates

I present an analysis of canine tooth size variability in male and female primates. The coefficient of variation (CV = SD X 100/mean) as an index of canine size variability proved to be dependent on mean canine size in males and, to a lower extent, in females. Therefore, variability tends to increase with increasing values of mean canine size. Using residuals from the regression of log SD on log mean canine size in male and female primates, I analysed the contribution of diet, habitat and mating system to canine size variability. Habitat and mating system are known to influence to a certain extent the degree of sexual dimorphism in canine size. Given the well-known relationship between sexual dimorphism and phenotypic variability, it was suggested that these factors might influence variability in canine size. Everything else being equal, males of polygynous species are characterized by more variable canine sizes than males of monogamous species. Habitat and diet did not contribute to the level of variability observed in either males or females. It is proposed that a high level of variability in canine size may be related to the likelihood that enlarged canines evolved as a result of male-male competition for mates in polygynous species.     

Postcanine tooth size in female primates

The results of many allometric studies of postcanine tooth size in mammals have not corresponded to expectations of tooth size based on energy requirements and dental function. The purpose of this study is to investigate the relationship between postcanine occlusal surface area, body size, and the metabolic demands of pregnancy and lactation in female primates. Tooth and body sizes from 38 primate species were taken from the literature to test two hypotheses: 1) females should have relatively larger teeth than males in order to masticate additional food for the energetic costs of reproduction; 2) taxa with the largest neonatal size (a measure of average metabolic costs of pregnancy and lactation) should have females with a greater degree of relative dental enlargement. The results show that relatively large female teeth are not found consistently in primate species. Females have less occlusal surface area than expected on the basis of the male tooth and body size regression in 21% of the species, and there is no correlation between relative female tooth size and relative newborn size across higher primate taxa. The degree of female dental enlargement is most closely related to degree of sexual dimorphism in body weight. The correlation between degree of body weight dimorphism and relatively larger postcanine teeth in females than in males is 0.87 in the 38 species. Species that are monomorphic in weight tend to be monomorphic in tooth size even though females apparently require more food than males.(ABSTRACT TRUNCATED AT 250 WORDS)     

Canine Length in Wild Male Baboons: Maturation,Aging and Social Dominance Rank

Canines represent an essential component of the dentition for any heterodont mammal. In primates, like many other mammals, canines are frequently used as weapons. Hence, tooth size and wear may have significant implications for fighting ability, and consequently for social dominance rank, reproductive success, and fitness. We evaluated sources of variance in canine growth and length in a well-studied wild primate population because of the potential importance of canines for male reproductive success in many primates. Specifically, we measured maxillary canine length in 80 wild male baboons (aged 5.04–20.45 years) from the Amboseli ecosystem in southern Kenya, and examined its relationship with maturation, age, and social dominance rank. In our analysis of maturation, we compared food-enhanced baboons (those that fed part time at a refuse pit associated with a tourist lodge) with wild-feeding males, and found that food-enhanced males achieved long canines earlier than wild-feeding males. Among adult males, canine length decreased with age because of tooth wear. We found some evidence that, after controlling for age, longer canines were associated with higher adult dominance rank (accounting for 9% of the variance in rank), but only among relatively high-ranking males. This result supports the idea that social rank, and thus reproductive success and fitness, may depend in part on fighting ability mediated by canine size.     

Static intraspecific allometry of the dentition in Otoletnur crassicaudatus

Adult static intraspecific allometry of tooth size was evaluated in a sample of 66 Otolemur crassicaudatus (34 male, 32 female). Tooth areas were calculated from mesiodistal and buccolingual measurements of canines and postcanine teeth of both arcades and were scaled to four viscerocranial measurements: bimaxillary width; maxillo-alveolar length; mandibular length and bigonial width. Individual tooth crown areas were also scaled to total skull length, body length and body weight. From the log-transformed analyses it is concluded that postcanine tooth size was unrelated to body length or weight, and poorly correlated to skull length or jaw size. Although viscerocranial size appears to be independent of body size, these measures are well correlated to skull length. It is shown that the longer the skull, the shorter and narrower the maxilla, and the longer and broader the mandible. Canines are shown to scale negatively allometric to skull length, hence, large animals will have relatively small canines.     

An analysis of canine size and jaw shape in some Old and New World non-human primates

An analysis of the relationship between the height of canine teeth, the length of the jaw and the height of the jaw joint above the occlusal plane was undertaken in catarrhine primates and some cebids. An inverse relationship was found in males between the angle
the jaw must be opened to clear the canine teeth and the height of the jaw joint above the occlusal plane, divided by the length of the lower jaw. A theoretical model is presented which can account for this phenomenon and which presumes selection pressure for alignment of the canine teeth when in use. In females, the angle the jaw must be opened to clear
the canine teeth was in most cases very small though in certain species elongated canines
were found.     

Evolutionary dental changes.

In the evolution of primates there has been a tendency towards reduction in jaw length and prognathism, mandibular canine size and first molar cusp number, and third molar presence. These oral structures were contrasted, and compared with cranial size, body height and weight, and finger length in 118 males and 102 females of the Burlington Growth Centre. Body weight was significantly related to canine width and to jaw length and prognathism. These relationships were stronger in the males than in the females. The evolutionary reduction in these dental dimensions may result from an evolutionary reduction in genetically determined body size. In the males the number of molar cusps was related to finger length and cranial height. Agenesis of third molars was related to the length of the maxilla in both sexes. In the females, canine width was related to the number of cusps of the first molars, agenesis of third molars, and length of a finger. Simultaneous reductions in dental structures were more frequent in the females.     

SEX DETERMINATION OF THE CALIFORNIA SEA LION (ZALOPHUS CALIFORNIANUS CALIFORNIANUS) FROM CANINE TEETH

Size of canine teeth from California sea lion ( Zalophus californianus californianus ) carcasses is shown to be useful in determining the sex of animals which have missing genitalia or which are otherwise of unknown sex. A total of 267 canine teeth from carcasses of 68 males and 43 females were measured along five axes. Of root and crown measurements of upper and lower canines, males and females overlapped only in root thickness of upper canines. A multivariate ANOVA showed a significant difference in the size of canines between upper and lower canines, and between males and females. Stepwise discriminant analysis produced discriminant functions for upper and lower canines for determining sex of unknown-sexed California sea lions. A separate set of canine teeth from 39 male and 49 female California sea lions was correctly classified without prior knowledge of sex by visual inspection and by the two discriminant functions.     

Folivory, frugivory, and postcanine size in the cercopithecoidea revisited

At a given body mass, folivorous colobines have smaller postcanine teeth than frugivorous cercopithecines. This distinction is a notable exception to the general tendency for folivorous primates to have relatively larger postcanine tooth rows than closely related frugivores. The reason for this anomalous pattern is unclear, but one potential explanation is that the difference in facial size between these two subfamilies confounds the comparison-i.e., it may be that the large postcanine teeth of cercopithecines are a consequence of their large faces. The goal of this study was to test this hypothesis. Phylogenetic comparative methods were used to examine the relationships among postcanine area, facial size, and body mass in 29 anthropoid primates, including eight colobines and eight cercopithecines. Results indicate that there is a strong and highly significant partial correlation between postcanine area and facial size when body mass is held constant, which supports the hypothesis that facial size has an important influence on postcanine size. Moreover, colobines have larger postcanine teeth relative to facial size than cercopithecines. Surprisingly, when facial size is held constant, the partial correlation between postcanine area and body mass is weak and nonsignificant. These results suggest that facial size may be more appropriate than body mass for size-adjusting postcanine measurements in some contexts. A phylogenetic comparative test of the association between diet and relative postcanine size (scaled using facial size) confirms that folivorous anthropoids are characterized by relatively large postcanine teeth in comparison to closely related nonfolivores.     

Metrical dental analysis on golden monkey (Rhinopithecus roxellana)

Dental variation in the Chinese golden monkey (Rhinopithecus roxellana) is here evaluated by univariate, bivariate, and multivariate analyses. Allometric analyses indicate that canines and P3s are positively, but other dimensions negatively scaled to mandible and maxilla, and to body size. With the exception of the mesiodistal dimensions of I₁ and M₃, and the buccolingual dimension of P₄, mandibular dental variables show similar scaling relative to body size. Analysis of residuals shows that males have significantly larger canine, P³ and buccolingual dimensions of the postcanine teeth (M² and M³) than females. A significant difference in shape between the sexes is found in the buccolingual dimension of the upper teeth, but not in the mandible. Unlike the situation in some other species, female golden monkeys do not exhibit relatively larger postcanine teeth than males. In fact, the reverse is true, expecially for M²s and M³s. The fact that most of the dental variables show low negative allometry to body size might be related a cold environment that has led to the development of larger body size with reduced energy loss. When the raw data are examined by Discriminant Function Analysis the sexes are clearly distinguishable.     

Canine dimorphism

Canine dimorphism in many primates is exaggerated, with males possessing enormous, sharp canines that project far beyond the occlusal plane of the other teeth and females having smaller, less projecting canines. Ever since Darwin,¹ canine dimorphism generally has been attributed to sexual selection. However, recent analyses suggest that the evolution of canine dimorphism is complex and that the sexual selection hypothesis is only part of the story.     

Morphological Variation in Populations of <Emphasis Type="Italic">Eulemur albocollaris</Emphasis> and <Emphasis Type="Italic">E. fulvus rufus</Emphasis>

Sexual dimorphism in body size and canine weaponry is commonly associated with high levels of male-male competition. When group living species do not rely heavily on male-male competition for access to females, sperm competition may represent a viable alternative strategy. Unlike most haplorhine primates, lemurs are typically monomorphic in body weight and canine height. We assessed variability of body mass dimorphism and canine size dimorphism in brown lemurs using morphometric data from 3 populations in southeastern Madagascar: Eulemur fulvus rufus, E. albocollaris, and hybrids of the species. We found significant male-biased canine dimorphism in E. albocollaris in conjunction with body-size monomorphism. We observed similar patterns in the hybrids, but E. fulvus rufus exhibited significant female-biased size dimorphism and canine monomorphism. Testes volume was relatively high across study populations. Thus, sperm competition appears to be strong in brown lemurs. E. albocollaris males combine sperm competition with large canines, but not higher body mass, indicating a difference in sexual strategy from most lemurs. Patterns of body mass and canine size dimorphism are not uniform across brown lemur populations, indicating that future work on these populations can explicitly test models that predict relationships between size dimorphism and various types of competition.     

Canine root development and morphology inMacaca nemestrina

Recently,Yoshikawa andDeguchi (1992) reported an unusually high frequency (40%) of two-rooted maxillary canines inMacaca fuscata females and a complete absence of this trait in males. In the present study, canine root development and morphology was examined using cephalographs taken on 50 male and 50 femaleMacaca nemestrina, and 20 male and 20 femalePapio cynocephalus for comparison with the Japanese macaque. The results showed no double-rooted canines present in either species in the upper or lower canines. This supports the general rule that, among primates, canines possess a single-root. It was further suggested that the two-rooted canines inM. fuscata may be the result of the founder effect, i.e. that the genes for this trait may have been carried by the initial populations when they arrived on the islands sometime during the middle to late Pleistocene.     

Sexual dimorphism in two subspecies of Ethiopian baboons (Papio hamadryas) and their hybrids

Sexual dimorphism in mammals has been related to such variables as absolute body size, ecology, and various aspects of social behaviour. Attempts to relate dimorphism to any of these variables have necessarily used small heterogeneous samples to represent the relevant species. We are concerned by the inevitable exclusion of any measure of variability in dimorphism and the consequent impossiblity of assessing the significance of observed interspecific differences. In this paper we describe aspects of sexual dimorphism in anubis,hamadryas, and hybrid baboons from Ethiopia. Samples are large enough to permit a measure of intrapopulation variability. Hamadryas baboons are more dimorphic than anubis in epigamic features, but not in postcanine dentition, nor, contrary to previous reports, in body weight or canine tooth size. Hybrid males are more hamadryas-like and hybrid females more anubis-like, as would be predicted by the proposed mechanism for the establishment of the hybrid zone, namely the capture of anubis females by hamadryas males.     

Intrasexual selection and phylogenetic constraints in the evolution of sexual canine dimorphism in strepsirhine primates

The goals of this study were to analyze the origin and function of sex differences in the size of canine teeth among Malagasy lemurs and other strepsirhine primates. These analyses allowed me to illuminate interactions between different mechanisms of sexual selection and to elucidate constraints on this sexually-selected trait. In contrast to central predictions of sexual selection theory, polygynous lemurs lack both sexual dimorphism in body size and male social dominance, but the degree of sexual dimorphism in the size of their canines is not known. A comparison of male and female canine size in 31 species of lemurs and lorises revealed significant male-biased canine dimorphism in only 6 of 13 polygynous lemur species. This result is in contrast to predictions of a hypothesis that would explain the lack of size dimorphism in lemurs as a result of high viability costs because canine teeth presumably have low maintenance costs and because they are used as weapons in male-male combat. Moreover, because females had significantly larger maxillary canines than males in only one lemur species, female dominance is not generally based on female physical superiority and selective forces favoring female dominance do not constrain sexual canine dimorphism in the sense of a pleiotropic effect. Contrary to predictions of sexual selection theory, species differences in canine dimorphism across strepsirhines were neither associated with differences in mating system, nor with the potential frequency of aggression. Variation in canine dimorphism was also unrelated to differences in body size, but there were significant differences among families, pointing to strong phylogenetic constraints. This study demonstrated that polygynous lemurs are at most subject to weak intrasexual selection on dental traits used in male combat and that traits thought to be under intense sexual selection are strongly influenced by phylogenetic factors.     

The lower jaw of an aegialodontid mammal from the Early Cretaceous of Mongolia

A partial lower jaw is described of an aegialodontid mammal, Kielantherium gobiensis Dashzeveg, 1975, from the Guchin Us beds of Mongolia (?Aptian or ?Albian). The jaw has four molars and four or five premolar loci. A count of P5 M4 is argued to be primitive for the Tribosphenida. McKcnna's interpretation of the postcanine dentition of Peramus as P5 M3 is accepted. It follows that the Peramura could not lead to the Tribosphenida, which apparently arose from unknown 'pantotheres' with not less than nine postcanine teeth.