A new species of Golunda (Rodentia, Muridae) from the Late Pleistocene of Indian Himalaya

The youngest fossil Golunda (Rodentia, Muridae) is described from the Late Pleistocene fluvio-lacustrine deposits, exposed at Dulam (Bageshwar), Kumaun Lesser Himalaya, India. The age of fossiliferrous horizon is estimated as 31,000 yr BP. A new species, Golunda dulamensis nov. sp. has highly derived characters, e.g., antero-posteriorly stretched molars, upper molars with more length and less width, stephanodonty, cusps in M₃ strongly inclined backward giving the molars a very stretched aspect, and metaconid and entoconid in M₃ forming almost straight lingual row of the cusps. G. dulamensis nov. sp. is most similar to present day G. ellioti but differs from the later slightly by larger size, a thin connection between t₄ and t₅ in M¹, and comparatively larger entoconid and very weakly developed antero-labial cusp in M₃. We suggest that highly specialized molars of G. dulamensis nov. sp. and present day G. ellioti are derivable through G. kelleri. We also propose that Golunda migrated from Asia to Africa, not from Africa to Asia as was thought by earlier workers.     

Sequences and timing of dental eruption in Bolivian captive-born squirrel monkeys (Saimiri sciureus)

Squirrel monkeys, colony-born from Bolivian parents, were studied to establish the sequences and timing of eruption for deciduous and permanent teeth. Infants were born with a naked gingiva, and in only one monkey was di₁ present at birth. The eruption of the lower deciduous teeth preceded their upper counterparts with the exception of di2, dc, and dpm2. No significant differences were found between the right and left quadrants of the mandible and maxilla. No significant sexual differences were found in the age of eruption. By the age of 14 weeks, all deciduous teeth had erupted. The sequence of eruption of the replacement teeth was different from that of milk teeth. The differences lie in the delayed eruption of canine teeth and in the inverted sequence, from the back to the front, of the premolar series. Significant sexual differences were found in total eruption (TE) for PM₃ and I² (P < 0.05) and highly significant differences (P < 0.01) in TE and initial eruption (IE) for C¹, females being more precocious than males. The age at which monkeys completed dental eruption was highly variable, 103–119 weeks for males and 89–112 weeks for females. Differences were found when our results were compared with those of Long and Cooper [1968] for Colombian squirrel monkeys.     

Dental sexual dimorphism and morphology in african colobus monkeys as related to diet

We considered the relationship between dental sexual dimorphism and diet in 542 specimens of olive, red, and black-and-white colobus. Using univariate statistical techniques, we examined 41 measurements of the maxillary and mandibular dentitions. The results reveal two trends of dental sexual dimorphism in black-and-white colobus wherein (i) maleColobus guereza andC. angolensis are generally larger than females throughout the dentition and (ii)C. satanas and, to a lesser degree,C. polykomos exhibit reduced sexual differences in the canine base and females are slightly larger than males in noncanine dimensions. Females of the red colobus,Procolobus (Piliocolobus) badius, are slightly larger than males in most noncanine measurements but canine sex differences are more pronounced than those of black-and-white colobus.Procolobus (Procolobus) verus, the olive colobus, is characterized by some of the largest canine sex differences, yet the sexes do not differ much in noncanine mean values. When patterns of sexual dimorphism are considered in terms of specific ecology and behavior, it is possible to relate sex differences, in part, to known dietary differences. For example, overall dental morphology and the trend of sexual differences inC. satanas andC. polykomos seem to be associated with the consumption of a diet rich in seeds. The pattern of dental sexual dimorphism inC. badius may also be influenced by dietary factors in that their patrilineal social organization could restrict female access to certain foods thereby affecting rates of attrition and creating selection pressure for larger teeth. Relatively less is known of the ecology and social organization ofP. verus but their dental sexual dimorphism is possibly less related to dietary factors than is the case for red or black-and-white colobus.     

A geometric morphometric analysis of hominin upper second and third molars, with particular emphasis on European Pleistocene populations

The study of dental morphology by means of geometric morphometric methods allows for a detailed and quantitative comparison of hominin species that is useful for taxonomic assignment and phylogenetic reconstruction. Upper second and third molars have been studied in a comprehensive sample of Plio- and Pleistocene hominins from African, Asian and European sites in order to complete our analysis of the upper postcanine dentition. Intraspecific variation in these two molars is high, but some interspecific trends can be identified. Both molars exhibit a strong reduction of the distal cusps in recent hominin species, namely European Homo heidelbergensis, Homo neanderthalensis and Homo sapiens, but this reduction shows specific patterns and proportions in the three groups. Second molars tend to show four well developed cusps in earlier hominin species and their morphology is only marginally affected by allometric effects. Third molars can be incipiently reduced in earlier species and they evince a significant allometric component, identified both inter- and intraspecifically. European Middle Pleistocene fossils from Sima de los Huesos (SH) show a very strong reduction of these two molars, even more marked than the reduction observed in Neanderthals and in modern human populations. The highly derived shape of SH molars points to an early acquisition of typical Neanderthal dental traits by pre-Neanderthal populations and to a deviation of this population from mean morphologies of other European Middle Pleistocene groups.     

Early Cretaceous mammals of Western Siberia: 2. Tegotheriidae

New specimens of the tegotheriid docodont Sibirotherium rossicum Maschenko et al., 2003, including a maxillary fragment with two posterior teeth, an isolated upper molar, and mandibular fragments with teeth from the Early Cretaceous Shestakovo locality are described. The dental formula of Sibirotherium is I_{1 + ?}C1P₆M_6?. The upper molars of Sibirotherium, with two main labial and three lingual cusps, are convergently similar to the molars of tribosphenic mammals. In the dentary, the symphysis is short and Meckel’s groove is reduced. Sibirotherium is similar in the structure of lower teeth to Tegotherium from the Upper Jurassic of Mongolia; it is the latest known representative of Docodonta.     

Craniofacial variation and dietary adaptations of African colobines

African colobine monkeys show considerable craniofacial variation among species, although the evolutionary causes of this diversity are unclear. In light of growing evidence that diet varies considerably among colobine species, we investigated whether colobine craniofacial morphology varies as a function of their diet. We compared craniofacial morphology among five African species: Colobus angolensis, C. guereza, C. polykomos, Piliocolobus badius, and P. verus. Matrix correlation analysis indicated a significant correlation between species-specific morphological distance and dietary distance matrices. The mechanical advantage of the masseter muscle was higher in seed-eaters (C. angolensis and C. polykomos) and lower in those that eat mainly young leaves (C. guereza, P. badius, and P. verus). Canonical correspondence analysis revealed that the durophagous colobines possess relatively wider bigonial breadths, anteroposteriorly shorter faces, shorter postcanine tooth rows, more medially positioned dental batteries, wider bizygomatic arches, and anteroposteriorly longer zygomatic arches. Under the constrained lever model, these morphological features suggest that durophagous colobines have the capacity to generate relatively greater maximum bite forces. However, no consistent relationship was observed between diet and variation in the mandibular corpus and symphysis, implying that robust mandibles are not necessarily adaptations for stress resistance. Factors that may influence mandibular robusticity include allometry of symphyseal curvature and canine tooth support. Finally, linear measures of mandibular robusticity may suffer from error.     

New dental remains of Anoiapithecus and the first appearance datum of hominoids in the Iberian Peninsula

New dental remains of the fossil great ape Anoiapithecus brevirostris are described from the Middle Miocene local stratigraphic series of Abocador de Can Mata (ACM) in els Hostalets de Pierola (Vallès-Penedès Basin, NE Iberian Peninsula). These specimens correspond to maxillary fragments with upper teeth from two female individuals from two different localities: left P³–M¹ (IPS41712) from ACM/C3-Aj (type locality; 11.9 Ma [millions of years ago]); and right M¹–M² and left P⁴–M² (IPS35027) from ACM/C1-E* (12.3–12.2 Ma). Relative enamel thickness is also computed in the latter individual and re-evaluated in other Middle Miocene hominoids from ACM, in order to better assess their taxonomic affinities. With regard to maxillary sinus development, occlusal morphology, molar proportions and enamel thickness, the new specimens show greater resemblances with the (male) holotype specimen of A. brevirostris. They differ from Pierolapithecus catalaunicus in displaying less inflated crests, a more lingually-located hypocone, and relatively lower-crowned molars; from Dryopithecus fontani, in the relatively thicker enamel and lower-crowned molars; from Hispanopithecus spp., in the more inflated crown bases, less peripheral cusps and more restricted maxillary sinus; and from Hispanopithecus laietanus also in the thicker crests, more restricted occlusal foveae, and relatively lower-crowned molars. The new specimens of A. brevirostris show some slight differences compared with the holotype of this species: smaller size (presumably due to sexual size dimorphism), and less distally-tapering M² occlusal contour (which is highly variable in both extant and extinct hominoids). The reported remains provide valuable new evidence on dental intraspecific variation and sexual dimorphism in Anoiapithecus. From a taxonomic viewpoint, they support the distinction of this taxon from both Dryopithecus and Pierolapithecus. From a chronostratigraphic perspective, IPS35027 from ACM/C1-E* enlarges the known temporal distribution of Anoiapithecus, further representing the oldest record (first appearance datum) of hominoids in the Iberian Peninsula.     

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.     

Dental morphology of Jews from Yemen and Cochin

60 dental plaster casts of Jewish adolescents, half of them children of immigrants from Yemen and half of them from Cochin (India), were investigated as to tooth measurements and morphologic traits. Each group was composed of an equal number of males and females. Cochini showed a sex specific dimorphism in tooth size, a relatively larger bucco-lingual diameter of upper and lower first premolars, lower frequency of Carabelli's tuberculum and in males larger tooth measurements than their Yemenite counterparts. The variability of ²I² was significantly higher in females than in males, and in Yemenite girls than in Cochini. The molar patterns were similar in both groups with regard to number and development of cusps and occlusal form of the mandibular molars.     

Hypocone and metaconule: identification and variability on human molars

Hypocone and metaconule variability was studied in a large sample of upper molars belonging to several human populations. The identification of these cusps does not generally show problems. However, on second and especially on third molars, it is occasionally difficult to decide if a little cup located on the crown distal border is a hypocone or a metaconule. The identification of supernumerary cusps located between the metacone and the hypocone seldom is clarified. We suggest the utility of differentiating if such cusps proceed the hypocone or metacone division and of using metacone variability in dental anthropology studies. An objective classification of the metacone size is proposed to standardize observations. Paper presented at the 4^th congress of the European Anthropology Association (Florence, Sept. 1984).     

Metric variability in the anterior dentition of African colobines

The anterior dentition of three species of African colobines (Colobus polykomos, C. badius, and C. verus) was investigated metrically and the results analyzed for three characters: (1) intraspecific tooth size relations, (2) sexual dimorphism, and (3) interspecific relations. Based on incisor size sequences C. polykomos and C. badius appear to be more closely related to each other than either is to C. verus. However, incorporating the results of a previous study on postcanine dentition the three species appear to be equally closely related. The magnitude of sexual dimorphism in canine size decreases from C. badius to C. verus to C. polykomos. Interspecific differences in the degree of canine size dimorphism may be attributed to differential intensities of male intrasexual selection; however, the interspecific differences in canine size dimorphism do not correspond to the interspecific differences in body size dimorphism.     

The relation of canine size to pattern and extent of attrition in baboons

For most genera of animals the association between dental morphology and diet is such that inferences concerning the diet can be made on the basis of the dentition alone. The canine is the one tooth that appears exempt from such generalisation and exhibits a wide range of variability of size and shape in all groups. In order to determine the effect of dimorphism of the canine on the dental apparatus, male and female specimens of Theropithecus and Papio baboons were examined. Occlusal relationships and dental pathology for 21 Theropithecus and 40 Papio skulls were recorded, and crown height measurements obtained for maxillary incisors, buccal and lingual molar cusps. Attrition was the most common and severe cause of abscess formation in older animals: the pattern of attrition differed in adult males and females, the latter showing more wear of the incisor and lingual molar cusps. Partial correlations for incisor, buccal and lingual molar cuspal crown height show a significant correlation between incisor and lingual cusp attrition in juveniles of both sexes and adult females (p < 0.01). Adult males show no correlation of attrition. It is proposed that the correlation of incisor and lingual molar cusp attrition is associated with anterior-posterior grinding movements, such as take place during incision, that the large canine present in the male limits such movements, the sharp blade-like canine being employed as a cutting tool. This use of the canine by reducing functional demands on other teeth, prolongs the utility of the dental apparatus, and hence the lifespan of its possessor.     

A new spalacolestine mammal from the Early Cretaceous Jehol Biota and implications for the morphology,phylogeny, and palaeobiology of Laurasian ‘symmetrodontans’

‘Symmetrodontans’ are extinct mammals characterized by having a reversed‐triangle molar pattern in which three main cusps define a triangular molar crown. This dental morpholgy has been regarded as being intermediate between the ‘triconodont’ tooth and the tribosphenic pattern characterizing therians; it is a key feature in taxonomy of Mesozoic mammals and one to understand mammalian evolution and palaeobiology. Here we report a new genus and species of ‘symmetrodontan’ mammal, Lactodens sheni, from the Early Cretaceous Jehol Biota, represented by a partial skeleton with dentary and upper and lower teeth with dental morphologies well‐preserved. The new species has a dental formula of three upper incisors, one canine, three premolars, and six molars/three lower incisors, one canine, five premolars and six lower molars, double‐rooted canines, extremely low‐crowned and transversely thin premolars, and acute angled molars. The dental morphologies of molars and peculiar deciduous premolars are similar to those of Spalacolestes from North America. The associated upper and lower dentitions from one individual animal helped to clarify tooth identification of some spalacotheriids represented only by fragmentary material. Phylogenetic analyses indicate a close relationship of the new species to North American spalacolestines and faunal interchanges between Eurasia and North America, thus supporting the notion that small‐bodied spalacotheriids were diverse and had a pan‐Laurasian distribution during the Early Cretaceous. Absence of the Meckelian groove suggests acquisition of the definitive mammalian middle ear in spalacolestines, and deciduous canines and premolars in the slim and extremely long dentary imply a faunivorous diet.     

The anatomy and systematic position of the early Miocene proconsulid from Meswa Bridge, Kenya

A small collection of fossil catarrhines was recovered from the early Miocene locality of Meswa Bridge in western Kenya between 1978 and 1980. The associated fauna from Meswa Bridge indicates an age older than 20 Ma. Much of the material has been briefly described previously, and its taxonomic status considered. The material can be assigned to a minimum of four individuals, all of which are infants or juveniles. Although the specimens were shown to belong to a distinct species of Proconsul, the taxon was not named, primarily because many of the specimens belonged to immature individuals. Nevertheless, the combined morphological features of the deciduous and permanent teeth allow the diagnosis of a new species of Proconsul, which is formally named here as P. meswae. It is a large-sized species, similar in dental size to P. nyanzae. The main features distinguishing it from all other previously named species of Proconsul are: incisors and deciduous incisors relatively low crowned; upper deciduous canines relatively higher crowned and more robust; molars and deciduous premolars relatively broader and higher crowned, with a more pronounced degree of buccolingual flare and better developed cingula; size differential between molars not as marked; dP₄ with a longer mesial fovea and smaller hypoconulid and distal fovea; P₄ relatively broader, with a better developed buccal cingulum; lower molars less rectangular with a longer mesial fovea, smaller distal fovea, more restricted talonid basin, and a tendency for a smaller hypoconulid; dP⁴ and upper molars with strongly buccolingually splayed roots; mandibular corpus in infants relatively deeper and more slender; maxilla with a well developed canine jugum and fossa. The broader and more flared molars with better developed cingula indicate that the Meswa Bridge species is more primitive than other species of Proconsul. The inference that it is a stem member of the Proconsul clade is consistent with the estimated age of the material.     

Stomach Fermentation in East African Colobus Monkeys in Their Natural State

The microbial fermentation in the stomachs of two monkeys, Colobus polykomos, collected in Kenya, was studied. The gas accumulated within the stomach contained H₂ but no CH₄. Volatile fatty acid concentrations were high, but accumulated acid prevented determination of the fermentation rate in untreated, incubated stomach contents. Upon addition of bicarbonate, a very rapid rate could be demonstrated. Some D- and L-lactate were in the stomach contents. Starchy seeds or fruits rather than leaves appeared to have been consumed. Microscopically, the most prominent microorganisms seen were large, very refringent cocci, possibly Sarcina ventriculi, and various smaller cocci and rods. The 28 cultured strains of bacteria included 14 Staphylococcus, 2 Streptococcus, 10 Propionibacterium, and 2 Peptostreptococcus. The culture count constituted 10 to 20% of the direct count. No protozoa or cellulolytic bacteria were found.     

Mitochondrial cytochrome b gene sequences of old world monkeys: With special reference on evolution of Asian colobines

The classification and phylogenetic relationships of the Old World monkeys are still controversial. For Asian colobines, from three to nine genera were recognized by different primatologists. In the present study, we have sequenced a 424 bp mitochondrial tRNA^Thr gene and cytochrome b gene fragment fromMacaca mulatta, Mandrillus sphinx, Mandrillus leucophaeus, Semnopithecus entellus, Trachypithecus vetulus, T. johnii, T. phayrei, T. francoisi, Pygathrix nemaeus, Rhinopithecus roxellanae, R. bieti, R. avunculus, Nasalis larvatus, andColobus polykomos in order to gain independent information on the classification and phylogenetic relationships of those species. Phylogenetic trees were constructed with parsimony analysis by weighting transversions 5 or 10 fold greater than transitions. Our results support the following conclusions: (1) the Old World monkeys are divided into two subfamilies; (2) that among the colobines,Colobus, the African group, diverged first, andNasalis andRhinopithecus form a sister clade toPygathrix; (3) that there are two clades within leaf monkeys, i.e. 1)S. entellus, T. johnii, andT. vetulus, and 2)T. phayrei andT. francoisi; (4) thatRhinopithecus avunculus, R. roxellanae, andR. bieti are closely related to each other, and they should be placed into the same subgenus; (5) thatRhinopithecus is a distinct genus; and (6) that the ancestors of Asian colobines migrated from Africa to Asia during the late Pliocene or early Pleistocene.     

Euxinomys galaticus N. G. N. Sp. (Muridae,rodentia, mammalia) du pliocene de çalta (Ankara,Turquie)

Among the abundant fauna of Mammals from Çalta, a new Murid was found: Euxinomys galaticus, characterized by its internal cusps which are very back-placed, its t1 separated from the t2 but linked to the t5 on the M¹. The inferior molars present a strong median longitudinal crest. This new genus. Euxinomys also contains «Parapodemus similis from the Odessa's Catacombs.     

Locking Yourself Out: Diversity Among Dentally Zalambdodont Therian Mammals

We review the evolution of dental zalambdodonty across therian mammals. Among zalambdodonts, there is little or no occlusion between the protocone and talonid basin and one of the central cusps of the upper molars (metacone or paracone) and the talonid basin of the lower molars are lost or reduced. Over two dozen genera of therian mammals show zalambdodont molars, including tenrecids, chrysochlorids, Solenodon, the marsupial mole Notoryctes, the extinct placentals Apternodus, Oligoryctes, Parapternodus, and Koniaryctes, and the extinct marsupials Necrolestes and Yalkaparidon. The chiropteran Harpiocephalus is nearly zalambdodont. Transformation series provided by paleontological or ontogenetic data, plus occlusal relationships, can be used to determine the homology of molar cusps in zalambdodont taxa. Zalambdodont dental specialization does not appear to have led to ecological specialization. With the important exception of golden moles and tenrecs, dentally zalambdodont taxa are less speciose than their nonzalambdodont sister taxa.