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1.
    
Studies of dental microwear have been used to relate tooth form to function in a variety of recent and extinct mammals. Probably the most important aspect of microwear analysis is the possibility of using it to deduce the diet of extinct animals. Such deductions must be based on comparative studies of modern species with known diets, but to date, only qualitative studies have been attempted and all have been based on small samples. Here we report quantitative differences in dental microwear between primate species that are known to have different diets. Occlusal facets with different functions have previously been shown to exhibit different microwear patterns. However, the differences between facets of one species are shown to be far less than those between homologous facets of different species. Study of seven species of extant primates shows that enamel microwear can be used to distinguish between those with a mainly frugivorous diet and those with a mainly folivorous one. Microwear can also distinguish hard-object feeders from soft-fruit eaters. The microwear of Miocene Sivapithecus indicus cannot be distinguished statistically from that of the chimpanzee, but it is different from that of the other species. On this evidence S. indicus was not a hard-object feeder and the adaptive significance of its thick molar enamel is at present unknown.  相似文献   

2.
Dental microwear analyses are beginning to provide new insights into the intricacies of jaw movement and tooth use in modern and extinct mammals. However, these analyses are also raising new questions that are best answered through studies of live animals with known diets. The process of taking dental impressions from live animals is a difficult one that presents problems different from those encountered in working with museum material. This report presents a review of some of those problems together with solutions that have been developed in the course of laboratory work with nonhuman primates. It also summarizes recent developments in dental casting.  相似文献   

3.
One problem with dental microwear analyses of museum material is that investigators can never be sure of the diets of the animals in question. An obvious solution to this problem is to work with live animals. Recent work with laboratory primates has shown that high resolution dental impressions can be obtained from live animals. The purpose of this study was to use similar methods to begin to document rates and patterns of dental microwear for primates in the wild. Thirty-three Alouatta palliata were captured during the wet season at Hacienda La Pacifica near Canas, Costa Rica. Dental impressions were taken and epoxy casts of the teeth were prepared using the methods of Teaford and Oyen (1989a). Scanning electron micrographs were taken of the left mandibular second molars at magnifications of 200x and 500x. Lower magnification images were used to calculate rates of wear, and higher magnification images were used to measure the size and shape of microwear features. Results indicate that, while basic patterns of dental microwear are similar in museum samples and samples of live, wild-trapped animals of the same species, ecological differences between collection locales may lead to significant intraspecific differences in dental microwear. More importantly, rates of microwear provide the first direct evidence of differences in molar use between monkeys and humans.  相似文献   

4.
Dental microwear analyses have raised new hopes and questions for functional morphologists. One hope is that analyses will allow insights into subtle dietary differences of extinct species. One major question is whether seasonal and/or habitat differences in dental microwear are reliably detectable. The extensive collections of Cebus nigrivittatus obtained by the Smithsonian Venezuelan Project allowed us to examine seasonal and habitat differences in dental microwear. Specimens were collected from three distinct ecological life zones that are distinguished by both the amount of rainfall and its seasonability. Environmental variation is generally correlated with variation in resource availability which, in C. nigrivittatus, affects diet. Published field studies indicate that these animals depend more on dry hard fruit and chitinous invertebrates during drier times and succulent fruits and caterpillars during wetter times of the year. As in previous microwear analyses, epoxy replicas were prepared from dental impressions, and the replicas were examined under a scanning electron microscope. Two micrographs were taken of facet 9 on M2 of each specimen. Mean values for the proportion of pits (vs. scratches), pit wdith, and scratch width were computed for each of 62 individuals and compared between ecological zones and collecting dates by using a multiple comparison test. Results indicate that, while seasonal differences in molar microwear in C. nigrivittatus are perhaps reliably detectable, 1) they are small in magnitude, 2) they are only detectable in certain ecological life zones, and 3) they are not of the order of magnitude that will obscure major interspecific differences in molar microwear such as those between C. apella and C. nigrivittatus.  相似文献   

5.
This study quantitatively examined molar microwear in nine species of extant small-bodied faunivorous primates and microchiropterans. Comparative analyses were performed within the food category faunivory, both between hard- and soft-object feeding faunivores and between primarily insectivorous and carnivorous taxa. Additionally, microwear in faunivores was compared to that reported in the literature for frugivorous and folivorous primates. The results indicated that although insectivores and carnivores could not be distinguished by microwear analyses, hard-object faunivores (i. e., those that primarily consume beetles or actively comminute bone) can be readily distinguished from soft-object faunivores (i. e., moth, caterpillar, or vertebrate flesh specialists). The hard-object faunivores consistently exhibited greater pit frequencies (in excess of 40%). Furthermore, comparisons of these microwear data on faunivorous mammals to previous work on frugivorous and folivorous primates (Teaford, 1988, pers. comm.; Teaford and Runestad, 1992, pers. comm.; Teaford and Walker: American Journal of Physical Anthropology 64:191–200, 1984) permitted three observations to be made. 1) Faunivores tend to have higher mean feature densities than either frugivores or folivores, although these differences are not consistently statistically distinct. 2) Faunifores and frugivores that feed on hard-objects have comparable mean pit frequencies. 3) Although it is impossible to distinguish faunivores and folivores on the basis of metric analysis of gross molar morphology, this distinction can be made on microwear criteria. Both hard- and soft-object faunivores exhibit much higher mean pit frequencies than primarily folivorous species. © 1993 Wiley-Liss, Inc.  相似文献   

6.
The average inbreeding coefficients of the highly consanguineous Fur and Baggara tribes of Western Sudan were 0.04167 and 0.04450, respectively. Two hundred ninety-eight subjects from the two tribes were tested for polymorphism of hemoglobins, seven red cell enzymes, and four serum proteins. The Baggara showed a higher gene frequency of HbS and TfD and lower gene frequency of GdA and PC compared to the Fur. Both tribes showed a low gene frequency of PGM1 and high frequency of G6PD deficiency when compared to other Sudanese tribes. In spite of the high degree of inbreeding, no significant deviation from the Hardy-Weinburg equilibrium was observed in either tribe. The effects of inbreeding seem to be offset by mixing between the two tribes on Gabal Marra Plateau. The flow of the sickle gene from the Baggara into the Fur and other Sudanese tribes is discussed.  相似文献   

7.
A recent experiment to evaluate the reliability of dental microwear as an indicator of diet seems to show that differences in diets fed to laboratory animals are not reflected by their tooth wear. We feel that these results are misleading, and reflect not so much the limits of microwear analysis per se, but rather result from the problems of design and execution inherent in any experimental simulation of natural feeding behavior. The experiment in question was flawed in several respects, and we think that changes in the methods and assumptions of the study are necessary before the experimental approach can yield meaningful results with which to test hypotheses about microwear analyses.  相似文献   

8.
Recently we noted the effects of experimental diets on microscopic dental wear in the American opossum and concluded that it might prove difficult to distinguish the microwear produced by an insectivorous diet from that produced by some kinds of herbivorous ones. We also noted that wear caused by gritty diets and those containing plant opal, although they might be confused with one another, are easily distinguished from other sorts of dietary wear. Our conclusions have been challenged on the basis that possibly we did not allow sufficient time in the experiments for diagnostic wear patterns to emerge. Additional data reported here show that this is not so. Even in our n “control” animals, fed a relatively soft unabrasive diet, enough time elapsed to produce significant dental wear. A new technique is described which for the first time allows the study of changing patterns of microscopic wear in a living animal over a period of time, thus allowing each animal to serve as its own control. A solution containing a broad-spectrum proteolytic enzyme when applied to the teeth of an anesthetized animal removes the proteinaceous coat (pellicle) which will otherwise obscure wear scratches. Precision dental impressions can then be made which reveal the details of the pattern of microwear on the teeth.  相似文献   

9.
  总被引:2,自引:0,他引:2  
Masticatory movements and molar wear facets in species of Tupaia, Galago, Saimiri, and Ateles have been examined using cinefluorography and occlusal analysis. The molars have been compared with those of a fossil series: Palenochtha, Pelycodus and Aegyptopithecus. The extant primates are almost identical in their feeding behaviour, the movements and timing of the masticatory cycle. Food is first puncture-crushed where the cycle is elongated, the power stroke attenuated and abrasion facets are produced on the molars. Chewing follows, the movements are more complex, the power stroke has two distinct parts and attrition facets are produced. In the primitive forms (Tupaia, Palenochtha), shearing blades, arranged in series (en echelon) were used to cut the food during the first part (Phase I) of the power stroke as the lower teeth move into centric occlusion. This mechanism has been progressively replaced by a system of blade-ringed compression chambers which cut and compartmentalise the food in Phase I. This is followed by an anteromedially and inferiorly directed movement away from centric occlusion (Phase II) in which the food is ground. In both extant and fossil series there has been a clear trend towards the elongation of Phase II with a corresponding reduction in Phase I. These results suggest that the observed changes in the morphology of the jaw apparatus have probably occurred within the limits set by a pre-existing behavioral pattern.  相似文献   

10.
11.
Mechanico-functional features of molar form were studied in Callithrix, Alouatta, Pithecia and Cebus. Molars of Callithrix and Alouatta are adapted to loading foods under relatively high occlusal pressure; those of Pithecia and Cebus, under relatively low occlusal pressure. General functional considerations suggest that these taxa are adapted to insectivorous, folivorous, frugivorous and omnivorous diets, respectively. The physical properties of foods, principally mechanical strength and deformability, determine the selective pressures involved in the evolutionary adaptation of molar form. A dietary classification based upon percentages of foods eaten does not always reflect morphological adaptations. Homologous parts of teeth and homologous parts of the masticatory cycle do not always subserve equivalent functions. The relevance of functional occlusal analysis for deciphering phylogeny and explaining evolutionary grades is stressed.  相似文献   

12.
A sample of individuals with different unilateral pathologies affecting the masticatory apparatus has been studied. Replicas of the same teeth (first or second molar) on both sides have been obtained and observed by SEM. The number, length and orientation of buccal striations have been determined for each individual. Differences in the microwear pattern have been observed between pathological sides. Each individual displays a particular striation pattern, especially referred to the striation number variables. It is concluded that individuals exhibiting pathologies likely to affect mastication should be excluded from studies relating striation patterns to diet.  相似文献   

13.
14.
    
Abstract

Many types of wear facets can be found in mammalian teeth. Some are related to the initial surface, others use the cross-section of the enamel as the main tool. In primary occlusal surfaces facets mark the gradual wear, that are related to a relatively late ontogeny. Facets in teeth with secondary occlusal surfaces, however, represent specific arrangements of crests of enamel and dentine. Such facets require some initial wear to become fully functional. The tooth morphology guarantees such facets to be effective for a long period of time. Therefore they can be discriminated as specialized facets. From the different types of facets three specialized ones were selected, blade facets, rasp-facets, and nipper-facets, because they ate widely distributed, function differently, and are comparable with mechanical tools. They are long lasting and differ in the amount of exposed dentine. The amount of dentine is used to differentiate phases during late ontogeny, the part of the life history, when teeth are exposed to wear. Consequently the various types of facets can be related to different ontogenetic phases. The relevant phases are prolonged at the cost of other ontogenetic phases. Therefore, the various specialized wear facets represent heterochronies within the ontogeny of teeth.  相似文献   

15.
Measurements of mandibular fossa depth and slope of the articular eminence were obtained for human skeletal samples chosen to represent a wide spectrum of subsistence strategies and oral function: hunter-gatherers (Eskimos, Australians), American Indians dependent to a variable extent on maize agriculture, and early twentieth century American whites and blacks. In the Eskimo and Australian samples, a generalized and steady increase in fossa depth and slope was observed with increasing functional age (tooth wear) through wear level 5 (of 8), followed by a levelling off or slight decrease in fossa depth in later wear levels on the anterior teeth and a sharp decrease in fossa depth in later wear levels on the molars. Although much less consistent due in part to extensive and early molar loss, patterns of variation in the remaining samples were characterized overall by a decrease in fossa depth and slope with increasing wear, especially on the molars. Further, in those samples with high incidences of posterior tooth loss, fossa depth was routinely less and the eminence more gently sloped in subsamples having experienced molar loss than in subsamples retaining all their molars. These data provide evidence that the temporomandibular joint (TMJ) undergoes continuous morphological alteration throughout adult life, and that these alterations are probably mediated by dental function. Moreover, they suggest that differences in patterning of such alterations may exist among human groups with contrasting patterns of tooth use.  相似文献   

16.
    
This study describes the molar enamel microstructure of the greater galago, based on SEM study of four individuals. Galago molar enamel consists primarily of radially oriented Pattern 1 prisms. However, the most superficial enamel is characterized by regions of poorly developed prisms or nonprismatic enamel, and Pattern 3 prisms can be found at depths intermediate and deep to the enamel surface. Orientations of prism long axes relative to wear surfaces differ among functionally distinct regions (cuspal facets, Phase I/II facets, and crushing basins). Consequently, orientations of enamel crystallites relative to these surfaces also differ. Because crystallites are the structural unit involved in enamel abrasion, these differences in orientation may have important effects on molar wear patterns. Crystallite orientations differ most between cuspal facets and Phase I/II facet surfaces. Cuspal facets are characterized by near surface-parallel interprismatic and surface-oblique prismatic crystallites. Previous experimental studies suggest that this arrangement is most resistant to wear when surface-normal (compressive) loads predominate. In contrast, prismatic and interprismatic crystallites intercept Phase I/II facet surfaces obliquely, an arrangement expected to resist abrasion when surface-parallel (shearing) loads predominate. Superficial enamel is preserved at most basin surfaces, indicating that these regions are subject to comparatively little abrasive wear. These results support the hypothesis that galago occlusal enamel is organized so as to resist abrasion of different functional regions, a property that may prove important in maintaining functional efficiency. However, this largely reflects constraints of occlusal topography on a microstructure typical of many mammals and thus does not appear to represent a structural innovation. © 1993 Wiley-Liss, Inc.  相似文献   

17.
18.
Lingual surface attrition of the maxillary anterior teeth (LSA-MAT) has been found in additional prehistoric Latin American Indian skeletons. LSAMAT was first observed in crania from an Archaic Brazilian site. This second finding occurs in teeth from Venado Beach, a late prehistoric site in Panama. LSAMAT is also present in some fragmentary specimens from the Archaic Cerro Mangote site in Panama. LSAMAT at Venado Beach is present in 57% of 28 adult crania. As in the Brazilian study, LSAMAT is associated with a high caries rate (82% of 50 adults; 11.7% of 852 permanent teeth). As first suggested, eating and processing of some type of abrasive carbohydrate food, such as manioc, is the possible cause of LSAMAT. However, other possible causes relating to habitation on or near marine coasts cannot be totally ruled out.  相似文献   

19.
    
Summary The luminal surface features and Junctional complexes from developing blood vessels in the rat central nervous system have been studied by high-voltage electron microscopy and scanning electron microscopy. Developing blood vessels exhibit three types of luminal projections; marginal folds or ridges at Junctional complexes, ridges not at Junctional complexes and microvilli. Both types of ridges are associated with troughs or depressions in the luminal surface of the endothelial cell. Those ridges not associated with Junctional complexes take part in the production of enclosed tunnels in the endothelial cell cytoplasm. Fusion of the external leaflets of Junctional complexes between adjacent endothelial cells occurred, initially, near the luminal surface of the blood vessel with other small fusion sites forming in the direction of the basal lamina secondarily. Further fusion activity to produce the zonula occludens type junction appeared to spread outwards from the smaller fusion sites.Supported in part by a NIH HVEM Travel Grant and the Medical College of Georgia  相似文献   

20.
In this study of thebelicoidal occlusal plane the relationships between tooth wear, the transverse slopes of mandibular molars and dental arch breadths were examined in 74 pre-contemporary Australian Aboriginal skulls. With increasing age and tooth wear the orientation of the mandibular occlusal surfaces increased towards the buccal. The differential occlusal orientation from first to third molars, present at eruption, tended to increase progressively with tooth wear. These functionally induced changes, together with regional differences in relative breadths of the maxillary and mandibular dental arches, are important in the development of abelicoidal occlusal plane.  相似文献   

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