Metric and taxonomic variations in the dentitions of two Asian cercopithecoid species: Macaca mulatta and Macaca speciosa

The primary molars and the first permanent molars of two Asian cercopithecoid species, Macaca mulatta and Macaca speciosa, were statistically described. Sexual dimorphism was not found related to tooth dimensions nor was there a significant difference between the right and the left sides. Generally, the teeth of Macaca mulatta were found to be larger than those of Macaca speciosa, and that this difference was significant for most tooth measurements. The discriminant function analysis reveals that the two species may be distinguished by tooth dimensions alone except in the dimensional range where over-lapping is expected.     

Histological study on the chronology of the developing dentition in gorilla and orangutan

The single previous study on tooth development in great apes (Dean and Wood: Folia Primatol. (Basel) 36:111–127, 1981) is of limited value because it is based on cross-sectional radiographic data. This study considers problems in defining stages of tooth development in radiographs of developing ape dentitions and provides data on tooth chronology in Pongo pygmaeus and Gorilla gorilla by using histological methods of analysis. Crown formation times were estimated in individual teeth, and an overall chronology of dental development was found by registering teeth forming at the same time by using incremental growth lines. The earlier radiographic study correctly identified the molar and second premolar chronology and sequence in great apes, but significantly underestimated crown formation times in incisors, first premolars, and canine teeth in particular. Ape anterior tooth crowns take longer to form than the equivalent human teeth, but the overall dental developmental period in great apes is substantially shorter than in humans. Gorilla root extension rates appear to be fast, up to approximately 13 μm/day. This rapid root growth, associated with early tooth eruption, appears to be the developmental basis for the observed differences in timing between developing dentitions in great apes and humans.     

Two macaque fossil teeth from the Japanese Pleistocene

Two fossil teeth of the Pleistocene macaque of Japan are stated to be those ofMacaca cf.fuscata. One of them is a lower canine tooth found in the Shiriya mine in northern Japan. It has been thought that the fossil assemblage of the Shiriya mine is of the late Pleistocene. The canine concerned is not distinguishable from the lower right one of the living female Japanese monkey. The other is a lower molar taken from the Ando quarry in western Japan. The fossil assemblage from the Ando quarry or from sites neighbouring the quarry indicates that the age of the molar can be traced back to the middle Pleistocene. The molar concerned has a somewhat buccolingually depressed crown as compared with that of the living Japanese monkey (Macaca fuscata).     

Banding patterns of the chromosomes of Presbytis cristatus pyrrhus and P. obscurus

The G- and Q-bands and the location of the nucleolar organizer regions (NOR) in the chromosomes of Presbytis obscurus and the Q- and C-bands of P. cristatus pyrrhus are described. Their chromosomes are compared to those of Macaca mulatta and to other Cercopithecidae and Hylobatidae. The origin of the two different banding patterns of pair no. 1 in our specimen of P. cristatus pyrrhus is discussed.     

Patterns of dental wear and the role of the canine in Cercopithecinae.

The importance of dental wear patterns in understanding masticatory functions in primates has long been appreciated. However, studies of wear patterns among populations of nonhuman primates are few. The purpose of this investigation is to establish the developmental aspects of dental wear in the Cercopithecinae and to describe certain relevant morphological traits. Studies were made of dental casts from 200 primate specimens of Macaca nemestrina, Macaca mulatta, and Papio cynocephalus. These casts were taken at four-month intervals, beginning at two years of age and continuing over a period of six to seven years. The wear pattern starts with the rounding and eventual flattening of the protoconid and protocone of the erupted first molars. Once this stage is reached, the hypoconid and metaconid of the mandibular, and the hypocone and paracone of the maxillary molars are rounded and eventually flattened. This pattern is maintained until the cusp tips are removed and the dentin exposed, however, the entoconid and metacone are not subjected to significant wear at this stage. Analysis of these dental casts and museum specimens has provided data on the development of dental wear during the maturation of these primates. The distribution of forces acting upon the teeth produce diagnostic patterns of wear, which provide evidence of the force location and magnitude. In examining the data, the hypothesis of canine guidance and its limitation of mandibular motion was evaluated. Specimens whose canines were removed demonstrate that the canines play no significant role in the development or maintenance of dental wear planes.     

Cercopithecoid canine tooth honing mechanisms

The form of the unworn male Cercopithecoid maxillary canine tooth (C') is effectively adapted for stabbing and slashing. Its essential features are maintained by wear against the mandibular canine (C₁) and first premolar (P₃) teeth. The cusp tip of C₁ is sharpened by reciprocal wear against C'. The distribution of apposing wear facets indicates that functional attrition results from honing activity largely distinct from mastication. Functional attrition also occurs in reduced form in females and is produced within the masticatory excursive range. The significance of the “sectorial” form of P₃ is analyzed. Its elongated mesiobuccal surface serves the dual purpose of honing the distal cutting edge of C' and functioning as a cutting block against which vegetation is stabilized and shredded by the cervical third of the distal cutting edge of C'. Behavioral aspects of honing are correlated with field observations linking tooth grinding with aggression, tension release, and communication. Parallel human behavior is cited and the suggestion is made that human tooth grinding with its highly charged emotional overtones is largely relict behavior that once had high survival value in a canine tooth honing context.     

Comparison of Leaf Plastochron Index and Allometric Analyses of Tooth Development in Arabidopsis thaliana

Abstract Two methods of analyses were used to investigate tooth development in serrate (se) mutant and wild-type Columbia-1 (Col-1) Arabidopsis thaliana leaves. There were almost twice as many teeth with deeper sinuses and two orders of toothing on the margins of serrate compared with Columbia-1 leaves. The main objective of this study was to test three hypotheses relative to the source of polymorphism in tooth development: (i) Teeth share similar growth rates and initial sizes, but the deeper teeth are initiated earlier in leaf development. (ii) Teeth share similar timing of initiation and growth rates, but the deeper teeth have a larger initial size. (iii) Teeth share similar timing of initiation and initial sizes, but the deeper teeth have a faster growth rate. Leaf plastochron index (LPI) was used as the time variable for leaf development. Results showed teeth in se were initiated at −27 LPI, 15 plastochrons earlier than those of Col-1. Serrate leaf expansion was biphasic, with the early phase expanding at half the relative plastochron rate of the later phase, which equaled the constant relative expansion rate of Col-1 leaves. Allometric analyses of tooth development obscured the interactions between time of tooth and leaf initiation and the early phase of leaf expansion characteristic of serrate leaves and teeth. Timing of developmental events that allometric analysis obscured can be readily detected with the LPI as a developmental index. Received 25 January 2000; accepted 17 March 2000     

Aberrant growth of maxillary canine teeth in male babirusa (genus Babyrousa)

A worldwide survey of babirusa skulls curated in museum and private collections located 431 that were from adult males and had retained at least one maxillary canine tooth. Eighty-three of these skulls were identified as exhibiting aberrant maxillary canine tooth growth. Twenty-four of the skulls represented babirusa from Buru and the Sula Islands, and forty-five skulls represented babirusa from Sulawesi and the Togian Islands. The remaining series of fourteen babirusa skulls originally came from zoo animals. Fifteen skulls showed anomalous alveolar and tooth rotation in a median plane. Twenty-nine skulls had maxillary canine teeth that did not grow symmetrically towards the median plane of the cranium. Fourteen skulls showed evidence that the tips of one or both maxillary canine teeth had eroded the nasal bones. Twenty-one skulls had maxillary canine teeth that had eroded the frontal bones. The teeth of two skulls had eroded a parietal bone. One skull had two maxillary canines arising from an adjacent pair of alveoli on the left side of the cranium. Three skulls exhibited alveoli with no formed maxillary canine teeth in them. Analysis suggested that approximately 12% of the adult male babirusa in the wild experience erosion of the cranial bony tissues as a result of maxillary canine tooth growth. There was no skeletal evidence that maxillary canine teeth penetrate the eye.     

Horizontal tooth displacement and premolar occurrence in elephants and other elephantiform proboscideans

Abstract

Modern elephants lack permanent premolars and their cheek teeth succeed one another by an unusual horizontal tooth displacement mechanism. The fossil record demonstrates that this mechanism characterises elephantimorph proboscideans and first evolved in the late Oligocene. Horizontal tooth displacement provides elephantimorphs with an adaptive advantage over more primitive proboscideans with vertical tooth replacement and concurrent function of all adult teeth. Premolars were lost convergently in diverse elephantimorph taxa with small or no lower tusks and foreshortened symphyses, including independently in crown elephant genera. New evidence reveals the presence of premolars in early species of Loxodonta and loss of premolars in the Loxodonta clade by the mid-Pliocene. Rare occurrences of premolars in mammoths support the hypothesis that these teeth were lost by suppression of genetic and molecular processes responsible for their development. Retention of premolars in Elephas planifrons indicates independent loss of premolars in Elephas and mammoths, and that Elephas had multiple migrations out of Africa, once pre- and once post-loss of premolars in the genus. Unfortunately, the effects of dwarfing are thought to obscure the phylogenetic affinities of fossil elephants from Sulawesi and Java in the genus Stegoloxodon that retain permanent premolars.     

ASPECTS OF CONE AND OVULE ONTOGENY IN CRYPTOMERIA (TAXODIACEAE)

The axillary complex of female cones of Cryptomeria is initiated as a tangentially extended triangular structure with a rounded apex. It is bilaterally symmetrical. Structures interpreted as prophylls are differentiated first, but they become insignificant in later development. They are succeeded by two successive pairs of lobes, each lobe being the common primordium for an adaxial ovule and a tooth. The ovule initially much exceeds the tooth. The apex of the complex has a diversity of fates and may differentiate as an ovule-tooth pair. A one-to-one relation between teeth and ovules may be lost by abortion of ovules. The initial relation between teeth and ovules is obscured in later development due to extension of tissues at the base of the complex associated with considerable enlargement of the teeth. Histogenesis of the various parts is described, together with the vascular system. There is a vascular supply to the tooth but not the ovule. The results support a direct comparison with the extinct transition conifers Pseudovoltzia and Aethophyllum but do not fully support Florin's generalized model for the arrangement of parts in the axillary complex of conifers.     

Developmental Aspects of Sexual Dimorphism in Hominoid Canines

We examined the histology of canine teeth in extant hominoids and provided a comparative database on several aspects of canine development. The resultant data augment the known pattern of differences in aspects of tooth crown formation among great apes and more importantly, enable us to determine the underlying developmental mechanisms responsible for canine dimorphism in them. We sectioned and analyzed a large sample (n = 108) of reliably-sexed great ape mandibular canines according to standard histological techniques. Using information from long- and short-period incremental markings in teeth, we recorded measurements of daily secretion rates, periodicity and linear enamel thickness for specimens of Pan troglodytes, Gorilla gorilla, Pongo pygmaeus and Homo sapiens. Modal values of periodicities in males and females, respectively, are: Pan 7/7; Gorilla 9/10; Pongo 10/10; and Homo 8/8. Secretion rates increase from the inner to the outer region of the enamel cap and decrease from the cuspal towards the cervical margin of the canine crown in all great ape species. Female hominoids tend to possess significantly thicker enamel than their male counterparts, which is almost certainly related to the presence of faster daily secretion rates near the enamel-dentine junction, especially in Gorilla and Pongo. Taken together, these results indicate that sexual differences in canine development are most apparent in the earlier stages of canine crown formation, while interspecific differences are most apparent in the outer crown region. When combined with results on the rate and duration of canine crown formation, the results provide essential background work for larger projects aimed at understanding the developmental basis of canine dimorphism in extant and extinct large-bodied hominoids and eventually in early hominins.     

Adaptive growth changes of the gonial region in Macaca mulatta

An experimental study of functional and adaptive growth changes of the gonial region associated with removal of all anterior teeth is being carried out through the life span of the Macaca mulatta monkeys. Radiographic cephalometry, using metallic implants as consistent points of reference and histological methods using in vivo tetracycline bone labeling, are the principal experimental techniques in the study. The present paper covers the results obtained from the longitudinal observations of the infant group from two to 24 months of age. The angular measurements of the gonial angle, linear measurements of the horizontal and vertical rates of growth in the gonial region were made in experimental and control groups. The data obtained from the angular measurements showed negative regression trends in both groups. The data from linear measurements of horizontal and vertical rate of growth exhibited positive linear regression trends with age. The histological findings, however, indicate differences between the two groups. Sections from the control group show some bone apposition in the gonial region, while experimental animals show extensive resorption. The results of this study show the inadequacy of standard anthropometric methods in the determination of adaptive growth changes of the gonial region at that early age.     

Ontogeny of postcanine tooth form in the ferret,Mustela putorius (Carnivora: Mammalia), and the evolution of dental diversity within the mustelidae

This study describes dental development within the ferret, Mustela putorius, through study of the form of the carnassial teeth and the upper first molar at progressive growth stages. Primordial teeth were serially sectioned in sagittal and transverse planes and three-dimensional reconstructions of tooth primordia were generated using MacReco software. Regional growth of the crown and asynchronous maturation of the dental tissues were observed in each tooth. The upper carnassial blade develops early and the tooth increases in length rapidly. Lingual growth of the upper carnassial is less pronounced and the protocone and its surrounding region mature late. The lower carnassial blade develops early and the talonid is late to mature. Development of the upper first molar differs from carnassial development in the early emphasis upon transverse growth and reduced lengthwise expansion. The early development of the carnassial blades in the ferret is shared with other carnivores, and may reflect the functional significance of this feature. Later stages of tooth ontogeny differ among carnivoran taxa and the specialized morphology of ferret teeth results from an apparently truncated period of late tooth ontogeny. This suggests that carnivoran species may share a common path of early development that specifies the ontogeny of homologous tooth features and that in later stages developmental differences result in species-specific tooth forms. J. Morphol. 237:69–90, 1998. © 1998 Wiley-Liss, Inc.     

Y-Chromosome and Mitochondrial Markers in Macaca fascicularis Indicate Introgression with Indochinese M. mulatta and a Biogeographic Barrier in the Isthmus of Kra

This is the first report of Y-chromosome introgression between primate species. We sequenced 3.1 Kb of Y-chromosome DNA and 1.5 Kb of mtDNA for 27 macaques of Fooden's (Folia Primatol. [1976] 25: 225–236) fascicularis species group and 5 outgroup taxa (Macaca sylvanus, Papio hamadryas, Theropithecus gelada, Allenopithecus nigroviridis, and Cercopithecus mona). Phylogenies constructed separately for the paternal and maternal data sets show a Y-chromosome paraphyly among lineages of Macacafascicularis, but a mitochondrial monophyly for the same individuals. The Y-chromosome topology depicts Indochinese Macaca fascicularis haplotypes joining with those of M. mulatta, followed by M. cyclopis and M. fuscata, before clustering with a clade of lineages of M. fascicularis from peninsular Malaysia, Indonesia, and the Philippines. These contrasting patterns of mitochondrial and Y-chromosome DNA, evaluated in the context of the evolutionary consequences of macaque sex-biased dispersal, present strong evidence for contemporary hybridization between Macaca fascicularis and M. mulatta in Indochina and a biogeographic barrier in the Isthmus of Kra.     

Tooth development and replacement in the Atlantic Cutlassfish,Trichiurus lepturus,with comparisons to other Scombroidei

Atlantic Cutlassfish, Trichiurus lepturus, have large, barbed, premaxillary and dentary fangs, and sharp dagger-shaped teeth in their oral jaws. Functional teeth firmly ankylose to the dentigerous bones. We used dry skeletons, histology, SEM, and micro-CT scanning to study 92 specimens of T. lepturus from the western North Atlantic to describe its dentition and tooth replacement. We identified three modes of intraosseous tooth replacement in T. lepturus depending on the location of the tooth in the jaw. Mode 1 relates to replacement of premaxillary fangs, in which new tooth germs enter the lingual surface of the premaxilla, develop horizontally, and rotate into position. We suggest that growth of large fangs in the premaxilla is accommodated by this horizontal development. Mode 2 occurs for dentary fangs: new tooth germs enter the labial surface of the dentary, develop vertically, and erupt into position. Mode 3 describes replacement of lateral teeth, in which new tooth germs enter a trench along the crest of the dentigerous bone, develop vertically, and erupt into position. Such distinct modes of tooth replacement in a teleostean species are unknown. We compared modes of replacement in T. lepturus to 20 species of scombroids to explore the phylogenetic distribution of these three replacement modes. Alternate tooth replacement (in which new teeth erupt between two functional teeth), ankylosis, and intraosseous tooth development are plesiomorphic to Bluefish + other Scombroidei. Our study highlights the complexity and variability of intraosseous tooth replacement. Within tooth replacement systems, key variables include sites of formation of tooth germs, points of entry of tooth germs into dentigerous bones, coupling of tooth germ migration and bone erosion, whether teeth develop horizontally or immediately beneath the tooth to be replaced, and how tooth eruption and ankylosis occur. Developmentally different tooth replacement processes can yield remarkably similar dentitions.     

Structure, attachment, replacement and growth of teeth in bluefish, Pomatomus saltatrix (), a teleost with deeply socketed teeth

Tooth replacement poses many questions about development, pattern formation, tooth attachment mechanisms, functional morphology and the evolution of vertebrate dentitions. Although most vertebrate species have polyphyodont dentitions, detailed knowledge of tooth structure and replacement is poor for most groups, particularly actinopterygians. We examined the oral dentition of the bluefish, Pomatomus saltatrix, a pelagic and coastal marine predator, using a sample of 50 individuals. The oral teeth are located on the dentary and premaxillary bones, and we scored each tooth locus in the dentary and premaxillary bones using a four-part functional classification: absent (A), incoming (I), functional (F=fully ankylosed) or eroding (E). The homodont oral teeth of Pomatomus are sharp, deeply socketed and firmly ankylosed to the bone of attachment. Replacement is intraosseus and occurs in alternate tooth loci with long waves of replacement passing from rear to front. The much higher percentage of functional as opposed to eroding teeth suggests that replacement rates are low but that individual teeth are quickly lost once erosion begins. Tooth number increases ontogenetically, ranging from 15–31 dentary teeth and 15–39 premaxillary teeth in the sample studied. Teeth increase in size with every replacement cycle. Remodeling of the attachment bone occurs continuously to accommodate growth. New tooth germs originate from a discontinuous dental lamina and migrate from the lingual (dentary) or labial (premaxillary) epithelium through pores in the bone of attachment into the resorption spaces beneath the existing teeth. Pomatomus shares unique aspects of tooth replacement with barracudas and other scombroids and this supports the interpretation that Pomatomus is more closely related to scombroids than to carangoids.     

The reproductive history of a hybrid female (Macaca mulatta ×Macaca fuscata)

In 1968 a female hybrid (Macaca mulatta ×Macaca fuscata) was born into the freeranging Arashiyama B troop of Japanese macaques (Macaca fuscata). At the age of 4 years this hybrid had her first offspring and by 1978 had accumulated eight descendants (five daughters, one son and two grandchildren). In this report the reproductive history of the hybrid is discussed and compared to the other non-hybrid members of the troop.     

A case of infanticide in a free-ranging group of rhesus monkeys (Macaca mulatta) in the jackoo forest,Simla, India

During field research on winter adaptation to a high mountain environment of the rhesus monkeys (Macaca mulatta), a newly established alpha male killed an infant less than 1 year old. This is the first case of infanticide witnessed in a natural free-ranging population ofM. mulatta. It seems likely that the infanticide was facilitated by the high population density in the available habitat during the winter.     

Evolutionary conservatism in arrangement of genetic material

The diploid number of the Rhesus macaque, Macaca mulatta, is 42. All chromosomes are biarmed and all constitutive heterochromatins are centromeric. The diploid number of the African Green monkey, Cercopithecus aethiops, is 60. Again all chromosomes are biarmed, but seven pairs possess very short second arms which are heterochromatic. The heterochromatins of remaining chromosomes are centromeric. Using G-banding and deleting the heterochromatic short arms, the chromosomes of the African Green monkey can be artificially fused to reconstruct a karyotype of the Rhesus with only one pair of unmatched small metacentrics. In addition to the Robertsonian type of translocations, several sets of centromere-telomere translocations were found. The latter type of translocation reduced three arms into two. Thus the fundamental number can be changed by two mechanisms: growing extra heterochromatic arms and the centromere-telomere fusions.