Coronal breadth of human primary anterior teeth

Original data for mesiodistal diameter of deciduous anterior teeth on 180 White children show: (1) mean size is smallest for the lower central incisor and largest for the upper canine, (2) means from combining widths on the left anterior teeth of each arch are larger in the maxilla than the mandible by 4.0 mm, (3) individual differences for widths of the upper central and lateral incisors extend from one child with these teeth of similar size to another child with the central incisor larger than the lateral by 2.3 mm, and (4) anterior tooth correlations are positive, varying from r = 0.4 for upper canine width with width of lower central incisor, to r = 0.8 for combined widths of left anterior teeth in the maxilla with combined widths of their antagonists. Comparative findings are drawn from investigations on Australian aborigines, South African Bushmen, Liberian Negroes, Tristan da Cunha islanders, Japanese, Japanese-Negro admixtures, Japanese-White admixtures, White groups living in several parts of Europe, and North American Whites. Among these ethnic groups, Australian aborigines have the largest deciduous anterior teeth. Composite means on each sex for North American Whites show boys to have slightly larger anterior deciduous teeth than girls.     

Premaxillary-maxillary suture asymmetry in a juvenile Gorilla. Implications for understanding dentofacial growth and development

A specimen of juvenile gorilla was found that had the premaxillary-maxillary suture coursing between the lateral deciduous incisor and deciduous canine on one side of the jaw, but between the central and lateral deciduous incisors on the other; in the latter, the suture also separates the alveolus of the lateral deciduous incisor from the crypt of the growing successional lateral incisor. Rather than dismiss this exception to the traditional dictum of tooth identification--which is based on the position to teeth relative to this suture--as some inconsequential anomaly, an attempt is made to understand how this can occur within the confines of present understanding of dentofacial growth and development and developmental theory. An hypothesis relating tooth and tooth class identification is presented in the context of ectomesenchymally predifferentiated stem progenitors and subsequent tooth class proliferation.     

A functional consequence of an ossified mandibular symphysis

According to most recent workers, the presence of fused symphyses in some mammals is explained by the common view that muscle force is transmitted better across a fused, as opposed to an unfused, mandibular symphysis. Recent theoretical work has cast doubt on the importance of fusion for simple force transmission by suggesting that force can also be transmitted efficiently across an unfused symphysis, an expectation that has since been confirmed by a number of observational studies. Perhaps the real significance of symphyseal fusion is that, in animals with upper and lower incisor tooth rows that apply large forces to relatively small resistant food items, muscle force from both sides of the head is reliably available only when the symphysis is fused. Independent movement between the two sides of the lower incisor row, permitted by a patent symphysis, allows the possibility that one side of the lower row will come into contact with the upper incisor row, dissipating all of the muscle force from that side. The dissipation of approximately half of the available jaw muscle force, allowed by a patent symphysis, cannot be ignored when attempting to explain the presence of fused symphyses if one accepts the idea that strong incisor biting is an important element in the masticatory apparatus of those primates and other mammals with fused mandibular symphyses.     

Static intraspecific allometry of jaws and teeth in Cercopithecus aethiops

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

The occurrence of upper canine teeth in Roe deer (Capreolus capreolus) from England and Scotland

Examination of the skulls of 133 Roe deer (123♂, 10♀) from seven areas of England and Scotland has shown that small canine teeth or their alveoli are occasionally found in the upper jaw of both males and females. These teeth do not penetrate the gum and are detected readily only by dissection or preparation of the skull. Evidence for the presence of canine teeth was found in three of the seven populations sampled. It is concluded that the frequency of occurrence in most of the populations examined is very low except in one where it is of the order of 17 %. It is not clear whether the upper canine is represented in both the deciduous and the permanent dentition.     

Allometric relations of teeth and jaws in man

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

贵州省鼠耳蝠属一新纪录——狭耳鼠耳蝠

2010年10月在贵州省荔波县进行翼手目动物调查过程中,于荔波县洞塘乡捕获14只鼠耳蝠,经鉴定为狭耳鼠耳蝠Myotisblythii。主要鉴别特征:体型中等,前臂长64.60(60.78～67.72)mm(n=14,SD=1.71);耳狭长;耳屏直而细长,顶端尖锐;第三指最长、第五指最短;后足长约为胫长之半;无距缘膜;尾长67.99(60.56～73.82)mm(n=14,SD=3.7);雄性个体无阴茎骨,阴茎长12.58(8.42～15.72)mm(n=5,SD=2.86);颅全长24.09(23.48～24.72)mm(n=6,SD=0.55);头骨窄长;听泡发达;矢状脊较低;上颌内门齿有1个主尖和1个小附尖,外门齿小,与上犬齿分离;第2上前臼齿(P3)稍位于齿列内侧。此种鼠耳蝠为贵州省翼手目新纪录。     

A new tritylodontid from the Kayenta formation of Arizona

Kayentatherium wellesigen. sp. now is a new tritylodont (Thcrapsida: Synapsida) from the Kayenta Formation of Arizona, U.S.A. Only the skull and parts of the lower jaw are known. The first upper incisor is apparently absent, so the dentition consists of one upper incisor followed, after a diastema, by a row of postcanines, which are replaced posteriorly. The cusp formula of these upper postcanines is 2, 2 (+ a ) 2, a being a tiny mesial cusp. The mean breadth/length ratio of these teeth is 1.59. Kayentatherium is related to the Tritylodon Bienotherium lineage, but is considerably more advanced than the latter, which is of Upper Triassic Lower Jurassic age. This indicates that the Kayenta formation must be Lower or Middle Jurassic age, with agrees with the conclusions of Welles.     

First evidence of the tooth eruption sequence of the upper jaw in Hyaenodon (Hyaenodontidae,Mammalia) and new information on the ontogenetic development of its dentition

Juvenile material with the main focus on the upper jaw of the fossil predator Hyaenodon was evaluated to study the tooth eruption sequence and to examine the ontogeny of its dentition in detail. The comparison in size of milk to permanent teeth indicates a growth rate of 12–16 % in Hyaenodon. The thin section of a deciduous canine of a North American taxon shows four dental rings. Based on the knowledge of recent carnivores, this implies an age of 3–4 years in the last stage of tooth eruption and thus a long juvenile phase. The mandibles ascertained the most recent established tooth eruption sequence for North American and European species. For the first time ever, juvenile material from Asia is documented and interpreted. This study likewise shows a difference in the sequence of the upper jaw: the first upper premolar erupts before the first upper molar in North American species, whereas the European taxa show an earlier eruption of the first upper molar. This fact further confirms the divergence between the Hyaenodon lineages from North America and Europe.     

沟牙田鼠的形态特征及分类地位探讨

沟牙田鼠是分布于中国四川西部和甘肃南部的一种罕见小型啮齿动物,迄今标本收藏甚少,种、属地位存在异议,有人认为应并入田鼠属。我们根据四川九寨沟自然保护区采到的16号不同年龄、性别的沟牙田鼠,就其牙齿形态和成年雄性的阴茎结构与其它田鼠类作了比较,发现其成体和幼体在M³和M₃形态上有很大不同。其他重要区别包括：上门齿宽大;下门齿外露部分很短,下门齿总长仅及下颌长的77％左右,远比其他田鼠小;M齿环呈圆弧形或豆形亦很特殊;成年雄性的阴茎骨近支烧瓶状,远支基部膨大与田鼠类差别很大。结果表明：沟牙田鼠属是有别于田鼠属的有效属。     

Extent and location of bone loss at dental implants in patients with peri-implantitis

Peri-implantitis is an infectious disease, which leads to loss of supporting bone around dental implants. To evaluate the extent and location of bone loss, 43 patients with peri-implantitis were examined. The bone loss was clinically measured at the time of dental surgery. Data revealed that 25% of subjects had bone loss associated with all their implants although the majority of the subjects had fewer than 50% of their implants affected by bone loss. A total number of 264 implants were examined and 131 of those had peri-implantitis associated bone loss. The pattern of bone loss at implants varied between and within subjects and location in the jaws. The highest proportion of implants with peri-implantitis was found in the upper jaw and within this group, at implants located in the incisor area of the upper jaw; the lowest was the canine area of the lower jaw. The highest proportion of implants that lost ≥ 2/3 of their bone support was found in the incisor area of the maxilla. We concluded that in the presence of peri-implant inflammation, bone quantity and characteristics may influence the progression of peri-implantitis bone loss at dental implants. We hypothesize that the ability of the bone to withstand occlusal forces will be altered as consequence of the loss of bone at the neck of the implants. To achieve an understanding of the local degradation of bone due to peri-implantitis, we need to analyze the microstructure of the bone as well the cellular biology of the peri-implant inflammation.     

Shh expression in a rudimentary tooth offers new insights into development of the mouse incisor

For teeth as for any organ, knowledge of normal development is essential for the proper interpretation of developmental anomalies in mutant mice. It is generally accepted that tooth formation is initiated with a single signaling center that, in the incisor region, is exclusively related to the development of the functional adult incisor. Here, using a unique combination of computer-aided three-dimensional reconstructions and whole mount in situ hybridization of mandibles from finely staged wild-type mouse embryos, we demonstrate that several Sonic hedgehog (Shh) expression domains sequentially appear in the lower incisor region during early development. In contrast to the single Shh expression domain that is widely assumed to be present in each lower incisor area at ED12.5-13.5, we identified two spatially distinct regions of Shh expression that appear in an anterior-posterior sequence during this period. The initial anterior, more superficially located Shh expression region represented the rudimentary (so-called deciduous) incisor, whereas only the later posterior deeper situated region corresponded to the prospective functional incisor. In the more advanced embryos, only this posterior Shh expression in the incisor bud was detectable as a precursor of the enamel knot. This study offers a new interpretation of published molecular data on the mouse incisor from initiation through ED13.5. We suggest that, as with Shh expression, other molecular data that have been ascribed to the progressive development of the mouse functional incisor at early stages, in fact, correspond to a rudimentary incisor whose development is aborted.     

Developmental origins and homologies of the hyracoid dentition

Understanding the origins of morphological specializations in mammals is a key goal in evolutionary biology. It can be accomplished by studying dental homology, which is at the core of most evolutionary and developmental studies. Here, we focused on the evolution and development of the specialized dentition of hyraxes for which dental homologies have long been debated, and could have implications on early placental evolution. Specifically, we analysed dental mineralization sequences of the three living genera of hyraxes and 17 fossil species using X‐ray computed microtomography. Our results point out the labile position of vestigial upper teeth on jaw bones in extant species, associated with the frequently unusual premolar shape of deciduous canines over 50 Ma of hyracoid evolution. We proposed two evolutionary and developmental hypotheses to explain these original hyracoid dental characteristics. (a) The presence of a vestigial teeth on the maxilla in front of a complex deciduous canine could be interpreted as extra‐teeth reminiscent of early placental evolution or sirenians, an order phylogenetically close to hyracoids and showing five premolars. (b) These vestigial teeth could also correspond to third incisors with a position unusually shifted on the maxilla, which could be explained by the dual developmental origin of these most posterior incisors and their degenerated condition. This integrative study allows discussion on the current evolutionary and developmental paradigms associated with the mammalian dentition. It also highlights the importance of nonmodel species to understand dental homologies.     

Development and size of the teeth of Macaca mulatta.

A cross-sectional sample of 151 skulls from Macaca mulatta of known age and similar rearing in U.S. Primate Centers was analyzed to determine age-related "norms" of stages of development and size of teeth. The stages of development from the follicle of a deciduous incisor in the fetus to completion of the root with apex closed of the permanent third molar were related to age. The age range observed for eruption of each tooth was noted and related to its stage of development. The crown of each erupted tooth was found to be completely developed, but growth of its root continued for a longer, indeterminate period. When a deciduous tooth was exfoliated, the crown of the permanent successor was found to be completed and root growth had begun. Measurements of both mesiodistal and faciolingual diameters and of crown length of the teeth in situ and of total length and root length on roentgenograms were examined for sexual dimorphism. The faciolingual diameter of the deciduous mandibular second incisor and of both second molars showed the greatest sexual dimorphism among both diameters of all deciduous teeth. The mesiodistal and faciolingual diameters of the mandibular premolars were found to be the best dimensions in discriminant functions for identifying sex in the absence of permanent canines.     

Incremental enamel development in modern human deciduous anterior teeth

This study reconstructs incremental enamel development for a sample of modern human deciduous mandibular (n = 42) and maxillary (n = 42) anterior (incisors and canines) teeth. Results are compared between anterior teeth, and with previous research for deciduous molars (Mahoney: Am J Phys Anthropol 144 (2011) 204-214) to identify developmental differences along the tooth row. Two hypotheses are tested: Retzius line periodicity will remain constant in teeth from the same jaw and range from 6 to 12 days among individuals, as in human permanent teeth; daily enamel secretion rates (DSRs) will not vary between deciduous teeth, as in some human permanent tooth types. A further aim is to search for links between deciduous incremental enamel development and the previously reported eruptionsequence. Retzius line periodicity in anterior teeth ranged between 5 and 6 days, but did not differ between an incisor and molar of one individual. Intradian line periodicity was 12 h. Mean cuspal DSRs varied slightly between equivalent regions along the tooth row. Mandibular incisors initiated enamel formation first, had the fastest mean DSRs, the greatest prenatal formation time, and based upon prior studies are the first deciduous tooth to erupt. Relatively rapid development in mandibular incisors in advance of early eruption may explain some of the variation in DSRs along the tooth row that cannot be explained by birth. Links between DSRs, enamel initiation times, and the deciduous eruption sequence are proposed. Anterior crown formation times presented here can contribute toward human infant age-at-death estimates. Regression equations for reconstructing formation time in worn incisors are given.     

Incisal biting in the mountain beaver (Aplodontia rufa) and woodchuck (Marmota monax)

Analysis of synchronously recorded cine-radiographs and electromyograms in two rodents (Aplodontia rufa and Marmota monax) demonstrates that jaw movements and muscle activiteis during incisal functions are distinctly different from those found during mastication. Movements during incisal biting are primarily along the midline, accompanied by symmetrical activity of the jaw adductor muscles. Most biting cycles do not end in contact between upper and lower incisors. When contact does occur, the lower incisors are dragged along the lingual surfaces of the upper incisors. Cropping, or tip-to-tip occlusion of upper and lower incisors, was not observed. Sharpening of the lower incisors, a behavior which may be unique to the Rodentia, was recorded in both A. rufa and M. monax. During sharpening, the lingual surface of the lower incisor is dragged across the tip of the upper incisor producing a lingual wear facet. Like incisal biting, sharpening movements are primarily confined to the midline, although there may be lateral movements in some sharpening cycles. Sharpening cycles are among the most rapid cyclic movements recorded in mammals, as the mean frequencies of sharpening are 11 cycles/s in A. rufa and 8 cycles/s in M. monax. © 1995 Wiley-Liss, Inc.     

Variation in body size and trophic morphology within and among genetically differentiated populations of the cichlid fish, Metriaclima zebra, from Lake Malawi

1. The cichlid fish Metriaclima zebra , common in Lake Malawi, feeds by filtering plankton from the water and by brushing items from sediment covered substrata. It inhabits isolated rocky reefs among which community structure, resource availability and gene pools are likely to differ. We speculated that body size and trophic morphology of M. zebra might vary concomitantly.
2. We quantified the extent of genetic, body size and trophic variation within and between populations of M. zebra from southern Lake Malawi. Specifically, we tested the hypotheses that: (i) local populations are genetically differentiated, (ii) local populations differ in jaw morphology, dentition and standard length (SL), and (iii) variation in size is correlated with variation in trophic morphology.
3. Local populations of M. zebra differed in mean SL and were genetically differentiated. Moreover, populations exhibited dissimilar oral jaw morphologies and dentitions, perhaps related to differences in feeding biology. Variation in jaw shape was largely restricted to the curvature of the distal tip of the dentary. Populations were characterised by individuals with oblique, upward or downward directed gapes. Dental patterns differed in the proportion of unicuspid teeth in all rows of each jaw (dentaries and premaxillae) and the spacing of teeth in affected rows.
4. Within populations, jaw and tooth shapes were correlated with body size. Smaller individuals possessed upward curving jaws and closely packed multicusped teeth, while larger individuals exhibited relatively downward-directed jaws with increasing numbers of widely spaced unicuspid teeth.
5. Metriaclima zebra populations have increased in mean SL over the last decade, in contrast to a decline among Lake Malawi pelagic cichlids. Differences in size may contribute to variation in trophic morphology and may track local environmental dynamics in this lacustrine system.     

Histological and three dimensional organization of the odontogenic organ in the upper incisor of 100 gm rats: comparison with the lower incisor.

The epithelial tissue forming the posterior aspect of the apical foramen in the upper incisor of the rat was reconstructed from 1 mum thick serial cross sections. Like the lower incisor, this portion of the odontogenic organ in the upper incisor was composed of a bulbous and a "U"-shaped part. However, the bulbous part was considerably blunter and the "U"-shaped part much larger in circumference in comparison to the lower incisor. Although no differences were found between the upper and lower incisor regarding the contents and the basic organization of cells within each part of the odontogenic organ, specific differences were found within the bulbous part in the upper incisor. There was a more definitive boundary between the outer dental epithelium and stellate reticulum, a more intimate relationship of cell streams to the stellate reticulum, and a noticeable lack of swirling of cells as part of the streams. These features suggest that the activity inside the bulbous part is less intense in the upper incisor than it is in the lower incisor. In addition, the relationships between the bulbous part, the "U"-shaped part and the root sheath part of the odontogenic organ and the enamel organ were described for the upper incisor.     

Le Fort I型截骨术定位平面的应用解剖学研究

目的：研究Le Fort I型截骨术与上颌牙根尖的关系,为临床合理制订截骨平面提供解剖学依据。方法：选择上颌牙槽清晰或出土后仍有牙保留的颅骨,在颅骨梨状孔下缘至上颌结节作一连线作为模拟Le Fort I型术式截骨水平,以上颌牙槽缘为标志,用游标卡尺测量每侧上颌各牙的牙槽缘至上述模拟截骨水平的距离及牙槽缘至各牙根尖端的长度,然后计算出上颌各牙根尖至Le Fort I型术式截骨线的距离。结果：上颌各牙相对的牙槽缘至Le FortI型术式截骨线的距离,从中切牙至第二磨牙逐渐缩小,右侧中切牙为21．09±1．53mm,左侧中切牙为20．96±1．64mm,右侧第二磨牙为14．94±1．52mm,左侧第二磨牙为14．95±1．59mm;上颌各牙根尖至Le Fort I型术式截骨水平的距离,从中切牙至第二磨牙也逐渐缩小,而两侧尖牙牙根尖距离Le Fort I型术式截骨线的距离右侧为4．49±1．74mm,左侧为4．69±2．14mm,第二磨牙牙根尖距离Le Fort I型术式截骨线的距离右侧为4．65±1．63mm,左侧为4．49±1．89,两侧尖牙牙根尖和第二磨牙牙根尖至Le Fort I型术式截骨水平的距离均比较接近。结论：上颌各牙根尖至LeFortI型术式截骨线的距离均在4mm以上,根据前牙中尖牙牙根尖的位置和后牙中第二磨牙牙根尖的位置,Le Fort I型术式截骨线水平在13、23（3｜3）根尖及27、27（7｜7）根尖上方4mm以上,按此平面作截骨水平较为安全,不易损伤牙根。