中华山蝠牙齿的脱换模式

笔者于1997年对中华山蝠(Nyctalus velutinus)牙齿的脱换模式进行了研究。共观察幼蝠200只次。中华山蝠初生仔共有22枚乳齿,齿式为2.1.2.0/3.1.2.0,各乳齿略向舌侧倾斜,除乳前臼齿齿冠不分叉外,其余乳齿齿冠均分为三叶。4d龄开始换齿,31d龄左右脱换完毕。乳齿的脱落顺序是:上颌,PM2→PM1→C1→I1→I2;下颌,I1→PM2.I2→I3→PM1→C1;恒齿萌生的顺序为:上颌,M1→PM2.C1→M2→PM1.M3→I1→I2,下颌,M1→I1.PM2→I2.M2→I3.PM1→C1→M3。     

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.     

Development of the dentition in Alligator mississippiensis: upper jaw dental and craniofacial development in embryos, hatchlings, and young juveniles, with a comparison to lower jaw development

Development of the upper dentition in Alligator mississippiensis was investigated using a close series of accurately staged and aged embryos, hatchlings, and young juveniles up to 11 days posthatching, as well as some young and old adult specimens. Studies from scanning electron microscopy, light microscopy, acetate and computer reconstructions, radiography and macroscopy were combined to elucidate the details of embryonic dental development, tooth initiation pattern, dentitional growth, and erupted functional dentition. The results were compared with those from the lower jaw and related to the development of other craniofacial structures. Approximately 17 early teeth in each jaw half develop as surface teeth, of which 13 project for 1 to 12 days before sinking into the mesenchyme. The first three teeth initiate directly from the oral epithelium at Ferguson stages 14-15 (days 15-19 after egg laying), before there is any local trace of dental lamina formation. All other teeth develop from a dental prolamina or lamina; and with progressive lamina development, submerged teeth initiate from the aboral end leading to the formation of replacement teeth. All teeth form dentin matrix, but 12 early teeth do not form enamel. Approximately 20 embryonic teeth are resorbed, 6 are transitional, and 42 function for longer periods after hatching. The embryonic tooth initiation pattern (illustrated by defining a tooth position formula) does not support the previous models of Odontostichi, Zahnreihen, and Tooth Families, each of which postulates perfect regularity. Up to three interstitial tooth positions develop between sites of primary tooth initiation, and families with up to five generations at hatching are at first arbitrarily defined.     

Tooth replacement in adult Xenopus laevis (Amphibia: Anura)

To determine the time scale of tooth replacement in adult Xenopus laevis (Daudin), three large females of similar size were kept in aquaria at 25 °C for ten weeks. They were anaesthetized twice weekly with MS 222 and impressions of their upper jaws were taken using thin sheets of dental gold-casting wax. Because the erupted tips of the teeth were small (100 μm), the impressions were enlarged by projection so that the presence or absence of a tooth at each locus in the jaw could be recorded. Each half of each animal's jaw was analysed separately and a statistical analysis of the records yielded results for the duration of the Replacement Cycle and Functional Life of the teeth. The range of the median Replacement Cycle time between specimens was 910–1,010h, that of the Functional Life 580–700 h and that of the Gap Period (the time over which loci were unoccupied by functional teeth) 230–420 h. A tentative time scale for the complete tooth development cycle (from tooth germ initiation to complete resorption) was calculated by extrapolation from the results and ranged from 59.07 to 71.29 days.     

第四纪响蜥(Tinosaurus)化石的首次发现

在陕西洛南张坪洞穴的第四系中采得一些响蜥类(Tinosaurus)化石,有保存相当完好的上下齿骨和齿列,这是响蜥在第四纪的首次报道,使该属化石的地史分布从早第三纪延伸到第四纪。新材料下颌骨较粗壮,但个体很小,有齿间沟,同时兼具亚洲种及北美种的某些特征,因此建立一新种Tinosaurus luonanensis sp．nov．。     

Eating with a saw for a jaw: Functional morphology of the jaws and tooth‐whorl in Helicoprion davisii

The recent reexamination of a tooth‐whorl fossil of Helicoprion containing intact jaws shows that the symphyseal tooth‐whorl occupies the entire length of Meckel's cartilage. Here, we use the morphology of the jaws and tooth‐whorl to reconstruct the jaw musculature and develop a biomechanical model of the feeding mechanism in these early Permian predators. The jaw muscles may have generated large bite‐forces; however, the mechanics of the jaws and whorl suggest that Helicoprion was better equipped for feeding on soft‐bodied prey. Hard shelled prey would tend to slip anteriorly from the closing jaws due to the curvature of the tooth‐whorl, lack of cuspate teeth on the palatoquadrate (PQ), and resistance of the prey. When feeding on soft‐bodied prey, deformation of the prey traps prey tissue between the two halves of the PQ and the whorl. The curvature of the tooth‐whorl and position of the exposed teeth relative to the jaw joint results in multiple tooth functions from anterior to posterior tooth that aid in feeding on soft‐bodied prey. Posterior teeth cut and push prey deeper into the oral cavity, while middle teeth pierce and cut, and anterior teeth hook and drag more of the prey into the mouth. Furthermore, the anterior‐posterior edges of the teeth facilitate prey cutting with jaw closure and jaw depression. The paths traveled by each tooth during jaw depression are reminiscent of curved pathways used with slashing weaponry such as swords and knifes. Thus, the jaws and tooth‐whorl may have formed a multifunctional tool for capturing, processing, and transporting prey by cyclic opening and closing of the lower jaw in a sawing fashion. J. Morphol. 276:47–64, 2015. © 2014 Wiley Periodicals, Inc.     

A functional interpretation of the varanid dentition (Reptilia, Lacertilia, Varanidae)

A cinéradiographic analysis of the feeding movements in Varanus bengalensis produced the following results. The mouth is opened by raising the head (upper jaw) rather than by lowering the lower jaw. Starting from the resting position, the muzzle unit is elevated around 9 degrees relative to the rest of the skull during jaw opening; the quadrate swings anteriorly around 21 degrees. During jaw closure, the snout is depressed around 15 degrees relative to the rest of the skull, hence 6 degrees beyond the resting position. The quadrate swings backwards around 27 degrees. Amphikinesis is interpreted as allowing a stronger posterior recurvature of the maxillary teeth in Varanus. This increases the holding effect of the teeth without increasing their length, an adaptation of Varanus to capture relatively large prey. The formation of plicidentine (dentine infolding) in the teeth of Varanus increases the surface of attachment of the teeth on the supporting bone. Moreover, the dentine lamellae take up tensile and compressive stresses along their long axes upon axial or vertical loading of the teeth. The slope of pleurodonty is modelled so as to minimalize shear stress on the surface of ankylosis upon axial or vertical loading of the teeth.     

On the geometry and mechanics of tooth position in the white shark,Carcharodon carcharias

The teeth of captured specimens, of prepared museum specimens, and of high-speed videotape images of the white shark, Carcharodon carcharias, were compared with respect to (1) deviation of each tooth from the animal's midline and (2) the crown angle of the functional teeth along the jaw margin. Tooth position was measured either directly using a meter stick apparatus or derived from tracings of the video footage. Tooth positions were not statistically unique in any region of the upper or lower jaw but demonstrated less variability in crown angle within 30° of the midline (71.48° ± 10°). Videotape analysis of feeding sharks indicated an 8.7° increase in crown angle of the centermost teeth during bites where the jaws were closed through an angle of 20–35° and a 15.7° reduction in this same parameter during jaw adduction through 35° or more. Such changes in tooth orientation (relative to the rear of the buccal cavity) are ascribed to flexure of the cartilaginous jaws and cranium by the cranial musculature and possibly also to sliding of the tooth bed over the jaw. Outward rotation of the teeth and jaw rami describes a plucking action during feeding or prey sampling, while larger bites rotate the frontmost teeth inward towards the gullet. Functionally, this may make the teeth more effective at grasping small prey items or gouging chunks from larger prey. However, testing of the load required to remove teeth showed no significant increase in tensile resistance with reduced crown angle. © 1995 Wiley-Liss, Inc.     

Associations in emergence age among permenent teeth

Associations in the timing of emergence among the permanent teeth of Boston children were obtained from a mixed longitudinal growth study of 414 Caucasian twin pairs examined annually. Correlations were estimated by the method of maximum likelihood for corresponding left-right teeth, upper-lower teeth, and all paired combinations from central incisor to second molar in a jaw quadrant of each sex. Strong positive correlations in emergence timing prevailed throughout the dentition. Principal component analyses on correlation matrices of jaw quadrant relations for boys and girls in the maxilla and mandible showed that three components effectively explained the emergence associations among the seven permanent teeth in each jaw quadrant. Factor analytic techniques further illustrated the nature of the three components and showed the emergence relations to be essentially the same in the maxilla and mandible for both sexes. The first component was a general maturation factor influencing all of an individual's teeth to be simultaneously early or late in emerging. The remaining two components were a molar factor, affecting almost exclusively the emergence timing of the permanent first and second molars, and a duration factor that affected the duration of the emergence process for non-molar teeth, contrasting particularly the incisors and premolars.     

联合方法测量工作长度应用于颌骨囊肿受累牙根管治疗的研究

目的：研究颌骨囊肿受累牙根管治疗中采用联合方法测量根管工作长度的效果。方法：选取36 例颌骨囊肿受累患牙需术前 根管治疗的患者,共135 颗患牙,186 个根管,随机分为两组,实验组（93 个根管）采用电测法联合纸尖法测量根管工作长度,对照 组（93 个根管）则采用电测法联合X 线法测量根管工作长度。对比两组根管充填后的充填效果。结果：实验组的根管恰填率为 90.32%,高于对照组的79.57%（P＜0.05）。结论：采用电测法联合纸尖法测量颌骨囊肿受累牙根管工作长度,准确率高,根管充填 效果好且安全。     

Tooth replacement in the teleost fish Prionurus microlepidotus Lacépède

Previous studies on tooth replacement in lower vertebrates have been plagued by a lack of common integrative approaches and methods, making it impossible to furnish a phylogenetic synthesis. This study is based on serial sections of the jaw of Prionurus microlepidotus. Each Toothgerm was characterized by its developmental stage and its position in the jaw. The relationship between the developmental stage of toothgerm and position in the jaw has been studied and expressed in several graphical illustrations. The following conclusions have been made: (1) The initiation of toothgerms in P. microlepidotus is governed by two Zahnreihen, which respectively initiate toothgerms on the lingual and labial side of the functioning teeth in an alternating pattern. (2) Therefore, functioning teeth in one locus are supplied by the alternate eruption of lingual and labial toothgerms. (3) Advancing of tooth replacement in each locus is independent of functioning teeth and their successors in adjacent loci. (4) The disorders of replacement patterns are caused by an alternated rate of eruption of successive toothgerms as a response to unusual shedding of the functioning teeth.     

Mechanical wear of the gastropod radula: a scanning electron microscope study

The wear sustained by the teeth of the highly mineralized radula of Patella vulgata and the unmineralized radula of Agriolomax reticulatus has been studied with the scanning electron microscope. The unworn teeth of P. vulgata have tall pointed cusps and wear is first seen as a chipping of the tips then as abrasion. There is a well defined abraded surface giving the worn teeth a chisel shape. In cleaved teeth fibres ˜ 800 Å in diameter are observed parallel to the axis of the tooth. Evidence is presented for chemical etching and for the existence of a surface coat on the tooth. A. reticulatus teeth show wear over their whole surface. With the aid of the grooves in the jaw caused by the teeth the role of the jaw in flattening the radula and protracting and retracting the odontophore is confirmed. From the arrangement of the abraded surfaces on the teeth of P. vulgata it was deduced that the teeth rows are abraded one at a time while on a convex surface at or near the bending plane.     

Structure and formation of ankylosis in Xenopus laevis

The structure of ankylotic teeth in Xenopus laevis was studied by light, transmission, and scanning electron microscopy as well as by microradiography in decalcified and undecalcified specimens. The mature teeth of Xenopus laevis are calcified from the crown to the base, fused to the jaw bone, and have no uncalcified area, such as a fibrous ring separating the tooth into the crown and pedicle. Microradiography shows that the mature tooth and jaw bone appear as an X-ray opaque area, except for the basal region of the dentine. This region is composed of an X-ray translucent area and an X-ray opaque thin layer on the lingual side of the translucent area. The mature tooth is composed of two differently calcified areas: (1) a highly calcified area, which makes up almost all of the tooth and contains a thin layer of the basal dentine on the lingual side, and (2) a lowly calcified basal dentine, which is fused to the jaw bone. Therefore, the lowly calcified area does not completely separate the dentine and jaw bone. Repeating banding patterns among the collagen fibrils differ among the dentine-forming area and the matrices of dentine and jaw bone. During the formation of ankylosis of the tooth germ, collagen bundles in the dentine-forming area accumulate directly on the surface of the jaw bone. Consequently, the mature teeth of Xenopus laevis fuse to the jaw bone directly without the mediation of the other structures.     

A NEW BASAL PTEROSAUR GENUS FROM THE UPPER TRIASSIC OF THE NORTHERN CALCAREOUS ALPS OF SWITZERLAND

Abstract:  A lower jaw with multicusped teeth and a number of unique characteristics was discovered in an extensive exposure of the Upper Triassic Kössen Formation in the Northern Calcareous Alps. The ramus of the jaw is high and dominated by a row of large, oval foramina that lies parallel to the tooth row. In addition, the anterior portion of the dentary exhibits a large number of nutritive foramina and small pits, which might indicate an association with a soft tissue structure and/or the presence of a keratinous cover of that area during life. All elements of the jaw are thin-walled and hollow, possibly pneumatic. Two teeth are preserved within the dentary. One is tricuspid and the other bears four cuSPS. The teeth are noticeably small in comparison with the overall size of the ramus, being only one-third of the height of the ramus. The teeth show a strong similarity to those of the well-known basal pterosaur genus Eudimorphodon , whose jaw morphology, however, clearly differs from the specimen described in this study. The dentition and the pneumatic bone structure make an assignment to the Pterosauria plausible. Based on the great number of distinct morphological characters the specimen is described as Caviramus schesaplanensis gen. et sp. nov.     

Arch form,tooth size,and occlusomandibular kinesis in the Ceboidea

Correlations between dental morphology, arch configuration, and jaw movement patterns were quantitatively investigated in 23 ceboid species to elucidate integrative aspects of occlusal functional anatomy in an adaptive and evolutionary context. Differential maxillary-mandibular arch widths are primary in guiding lateral jaw movements. These movements are characterized according to their associated condylar shifts as either predominantly translatory or rotational. Predominantly translatory movements result from peripheral contact relationships between maxillary arches which are considerably wider posteriorly than their opposing mandibular arches. The greatest degree of mandibular movement is in the molar region in functional association with wide “primitive” maxillary molars, narrow mandibular molars, constricted maxillary intercanine widths, and narrow maxillary incisors. In contrast, predominantly rotational masticatory jaw movements result from differential arch widths which are greatest in the maxillary canine and incisor regions. Here most jaw movement is in the anterior segment and this is reflected in small maxillary-mandibular molar width differences, a high degree of premolarization, wide-set maxillary canine teeth, and wide maxillary incisors. Possible selectional factors in the putative evolution of rotational predominance in mastication from the more primitive translatory pattern are discussed.     

Age and wisdom teeth in Nigeria

An attempt has been made to estimate the eruption age of wisdom teeth in the North Nigerian population. The present study was carried out on 654 boys and 584 girls of age groups ranging from 11-23 years. From the data collected estimates have been provided for the eruption age of the third molar. In general, teeth of the lower jaw erupt before those of the upper jaw. The teeth on the left side erupt earlier than those on the right side. The wisdom teeth erupt little earlier amongst boys (18 years) as compared with girls (18.5 years). In general, the wisdom teeth erupt in Nigerians with some constancy between the age of 15 and 21. The wisdom teeth fail to erupt in 5% of the individuals.     

Tooth size and arcadal length correlates in man

Intra-arcadal mesiodistal and buccolingual tooth size correlations were evaluated in a sample of 125 caucasoids with ideal occlusion. Dental dimensions were corrected for arcade mength (as a measure of jaw size) by a series of regression analyses of each mesiodistal dimension on the sum of the mesiodistal dimensions within each arcade. Regression coefficients of tooth dimension on arcade length were calculated to gain an insight into the dimensional sensitivity of individual teeth to arcade length variation. The data presented here suggest a strong association between arcadal length (jaw size) dependence, and the dimensional stability of individual teeth. When corrected for arcade length, a definite pattern of tooth size correlation emerges: postcanine maxillary and mandibular teeth are negatively correlated to the anterior teeth and are positively correlated to one another. The hypothesis is developed that anterior and postcanine teeth should be viewed as two separate and negatively size-correlated units, beyond the boundaries of the four morphological tooth classes. Recognition of this basic dichotomous size arrangement within each jaw allows for a reassessment of some of the problems associated with hominid dental evolution.     

Jaw muscles in older overdenture patients

Objective: To determine, using computer tomography (CT), whether the retention of a small number of teeth in the older adult used to support overdentures could affect the cross‐sectional area (CSA) and X‐ray density of two jaw closing muscles. Design: Cross‐sectional study of a group of older patients subdivided into dentate, edentulous and those wearing overdentures supported by two to five teeth. Subjects: The sample consisted of 24 subjects aged 55–68 years. Outcome measures: CSA and X‐ray density of two jaw closing muscles, masseter and medial pterygoid were measured and evaluated using CT. Results: There were no significant differences between left and right jaw muscles, but the CSA of the masseter muscles were significantly larger than the medial pterygoid muscles. The CSA of the masseter and medial pterygoid muscles was significantly smaller in edentulous subjects compared with dentate subjects but no significant difference was observed between subjects wearing overdentures and those with a natural dentition. No significant differences were observed with the X‐ray density between different muscles or dental states. Conclusion: The retention of a small number of teeth in the older adult used to support overdentures appears to sustain the CSA of two jaw closing muscles and therefore could enhance these patients’ masticatory ability compared with those who were edentulous.     

The venom apparatus of the globiferous pedicellariae of the toxopneustid Sphaerechinus granularis (Echinodermata,Echinoida): Fine structure and mechanism of venom discharge

Summary Globiferous pedicellariae of Sphaerechinus granularis are venomous defensive appendages consisting of a stalk bearing a head made of three movable jaws. Each jaw is supported by a calcareous valve ending with a terminal grooved tooth. A venom apparatus is located in each jaw and consists of a venom gland surrounded by a muscular envelope and terminating in a duct which completely encircles the terminal tooth of the valve. Contrary to previous statements, the duct does not lie inside the groove of the terminal tooth. In mature pedicellariae, the venom is stored in intracellular vacuoles of highly differentiated cells which are no longer active. The cells fill the whole space of the venom gland which is without a lumen; they are segregated into two types that occur in distinct regions and differ from each other by morphological and staining properties of their secretions. Upon contraction of the muscular envelope, the venom is released via a holocrine mechanism and infiltrates the predator's tissues through the wound inflicted by the three calcareous teeth of the valves. In no case is the venom emitted through the tooth groove.     

Numeric anomalies of teeth in concomitant hypodontia and hyperdontia

Variations in tooth number in children, each of whom had supernumerary teeth and agenesis of teeth, is described. Among the 11, seven had cleft lip and palate, and two had clefting syndromes; two children had dental anomalies only. Only children who had both supernumerary teeth and congenitally missing teeth outside the area of the cleft alveolus were included. Concomitant hypodontia and hyperdontia were observed in the same dentition in nine subjects, in the same jaw in eight subjects, and in the same jaw quadrant in only three subjects. Supernumerary teeth and agenesis of teeth were observed simultaneously more often in the permanent dentitions than in the deciduous dentitions or in both dentitions simultaneously. The overall number of supernumeraries was 10 in the deciduous dentition and 14 in the permanent dentition of the 11 subjects. The number of congenitally absent teeth was 14 in the deciduous dentition and 40 in the permanent dentition. The etiology of concomitant hypodontia and hyperdontia is difficult to explain. It may result from disturbances in migration, proliferation, and differentiation of neural crest cells or interactions between the epithelial and mesenchymal cells during the initiation of odontogenesis.