Biplanar X-ray motion analysis of the lower jaw movement during incisor interaction and mastication in the beaver (Castor fiber L. 1758)

The first biplanar X-ray motion analysis of mastication and food processing for Castor fiber is presented. While particles are chipped off interaction of incisors involves variable movements of the lower mandible and thus incisors. After jaw opening the tip of the lower incisors can reach different positions anteriorly of the upper incisors. Then the mandible moves upwards and backwards and brings the tips of the incisors into contact. The lower incisors slide along the wear facet of the upper to the ledge when the cheek teeth occlude. The glenoid fossa and lower jaw condyle are in close contact during incisor contact and no transverse movements are observed. Mastication involves interaction of the cheek teeth with no contact of the incisors. When the cheek teeth are in occlusal contact the mandible is moved forward and transverse, or mediolateral. In consecutive power strokes the jaw is moved alternately to the right and left side. When the jaw opens it is brought into a more central but not totally centred position. During mastication the condyles are positioned posteriorly to the glenoid allowing lateral movement of the mandible. The lateral movement is particularly noticeable in the anterior part of the mandible. With the lateral movements of the incisors one glenoid has to move posteriorly, the other anteriorly.     

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.     

Feeding behavior,mastication, and tooth wear in the western tarsier (Tarsius bancanus)

We assessed feeding and masticatory function in western tarsiers, Tarsius bancanus,from field study, from videotaped recordings of the feeding and chewing behavior of wild-caught animals in temporary captivity, from dissections of the muscles of mastication, and from scanning electron microscopic (SEM) examination of wear features of the teeth. Ingestion of large items of animal prey is made possible by the animal’s extremely wide gape. Anterior translation of the knob-like mandibular condyle in the anteroposteriorly elongated mandibular fossa makes possible a gape angle of 60–70‡. We observed two means of ingestion of grasshopper prey: ingestion by mastication, in which the postcanine teeth sever and reduce bites of the food as it is thrust into the mouth cavity, and repeated gape-shove sequences, during which the tarsier pushed grasshoppers of large diameter into the anterior part of its mouth and attempted to sever a bite with its anterior teeth. Morsels were successfully severed after three to five such sequences, and reduced quickly,with relatively few powerful, crushing chews. The insect cuticle was not evenly comminuted during mastication. We observed a marked side-to-side grinding component in the normal chewing cycle of T. bancanuson videotape and confirmed it by SEM. The main jaw adductors are bulky, long-fibered muscles that can accommodate wide grapes and still generate, at wide degrees of gape,the high occlusal pressures necessary to fracture thick chitinous exoskeletons of the scarabid beetles that form a substantial element of the western tarsier’s diet.     

Three-dimensional dynamical capabilities of the human masticatory muscles

Many habitual human jaw movements are non-symmetrical. Generally, it is observed that when the lower incisors move to one side the contralateral condyle moves forwards onto the articular eminence, whereas the ipsilateral condyle stays in the mandibular fossa, moving slightly to the ipsilateral side. These jaw movements are the result of contractions of active masticatory muscles and guided by the temporomandibular joints, their ligaments and passive elastic properties of the muscles. It is not known whether the movements are primarily dependent on passive guidance, active muscle control or both. Therefore, the objective of this study was to analyse the interplay between these factors during non-symmetrical jaw movements. A six-degrees-of-freedom dynamical biomechanical model of the human masticatory system was used. The movements were not restricted to a priori defined joint axes. Jaw movement simulations were performed by unilateral activity of the muscles. The ligaments or the passive elastic properties of the muscles could be removed during these simulations. Laterodeviations conform to naturally observed ones could be generated by unilateral muscle contractions. The movement of the lower incisors was hardly affected by the absence of passive elastic muscle properties or temporomandibular ligaments. The latter, however, influenced the movement of the condyles. The movements could be understood by analysing the combination of forces and torques with respect to the centre of gravity of the lower jaw. In addition, the loading of the condyles appeared to be an important determinant for the movement. This analysis emphasizes that the movements of the jaw are primarily dependent on the orientation of the contributing muscles with respect to this centre of gravity and not on the temporomandibular ligaments or passive elastic muscle properties.     

棕色田鼠与甘肃鼢鼠咀嚼肌结构和功能的比较

为了解棕色田鼠与甘肃鼢鼠对食物的适应机制, 对它们的咀嚼肌及相关的骨学特征做了比较解剖, 并运用生物力学原理分析下颌运动方式及食物加工过程的咀嚼效率。结果表明, 两个种的下颌的咀嚼均以水平面的前后向运动为主, 研磨加工植物纤维。相应地, 咀嚼肌、牙齿及相关的骨骼形态也具有一系列与此运动方式和功能相适应的结构特征, 如彼此平行的左右侧颊齿列、沟槽状的下颌关节窝以及咬肌的排列位置前移等。此外, 两个种具有几乎相同的门齿切割效率和臼齿咀嚼效率。两个种的上述相似特征与它们有着相似的食物结构是一致的。     

Aspects of masticatory form and function in common tree shrews,Tupaia glis

Tree shrews have relatively primitive tribosphenic molars that are apparently similar to those of basal eutherians; thus, these animals have been used as a model to describe mastication in early mammals. In this study the gross morphology of the bony skull, joints, dentition, and muscles of mastication are related to potential jaw movements and cuspal relationships. Potential for complex mandibular movements is indicated by a mobile mandibular symphysis, shallow mandibular fossa that is large compared to its resident condyle, and relatively loose temporomandibular joint ligaments. Abrasive tooth wear is noticeable, and is most marked at the first molars and buccal aspects of the upper cheek teeth distal to P². Muscle morphology is basically similar to that previously described for Tupaia minor and Ptilocercus lowii. However, in T. glis, an intraorbital part of deep temporalis has the potential for inducing lingual translation of its dentary, and the large medial pterygoid has extended its origin anteriorly to the floor of the orbit, which would enhance protrusion. The importance of the tongue and hyoid muscles during mastication is suggested by broadly expanded anterior bellies of digastrics, which may assist mylohyoids in tensing the floor of the mouth during forceful tongue actions, and by preliminary electromyography, which suggests that masticatory muscles alone cannot fully account for jaw movements in this species.     

Size and shape of the mandibular condyle in primates

The relationships between the size of the articular surface of the mandibular condyle and masticatory muscle size, tooth size, diet, and biomechanical variables associated with mastication were studied by taking 12 measurements on skulls of 253 adult female anthropoid primates, including three to ten specimens from each of 32 species. In regressions of condylar length, width, or area against body weight, logarithmic transformations substantially improve the fit of the equations compared with untransformed data. There is a strong relationship between condylar measurements and body weight, with all correlations being .94 or higher. The slopes of the allometric regressions of length, width, and area of the condylar head indicate slight positive allometry with body size. Folivorous primates have smaller condyles than frugivorous primates, and colobines have smaller condyles than cebids, cercopithecines, or hominoids. When colobines are eliminated, the differences between frugivores and folivores are not significant. However, the two species with the relatively largest condyles are Pongo pygmaeus and Cercocebus torquatus, suggesting that there may be a relationship between unusually large condylar dimensions and the ability to crack hard nuts between the teeth. Cranial features having strong positive correlations with condylar dimensions include facial prognathism, maxillary incisor size, maxillary postcanine area, mandibular ramus breadth, and temporal fossa area. These data are interpreted as indicating that relatively large condyles are associated with relatively large masticatory muscles, relatively inefficient mandibular biomechanics, and a large dentition. These relationships support the growing evidence that the temporomandibular joint is a stress-bearing joint in normal function.     

Mastication in springhares,Pedetes capensis: A cineradiographic study

Analysis of lateral and dorsoventral radiographic films shows that ingestion, transport, and mastication in Pedetes capensis (Rodentia) are cyclic and their movement patterns are essentially similar for the three food types offered. During the ingestion cycle, closing of the mouth is accompanied by a backward translation of the condyles, so that movement is predominantly orthal. During the opening stage, the extent of the anterior condylar translation is smaller. As a result the mandibular incisors move ventrally and posteriorly. During the ingestion cycles, food is transported to the back of the tongue, with the transverse rugae and the folds of the upper lip playing important roles. Springhares show a bilateral masticatory pattern; food is chewed on both sides simultaneously. During chewing, the condyles lie in their most forward position at maximum opening of the mouth. The mouth is closed by rotation of the lower jaw around the temporomandibular joint coupled with posterior condylar translation. At the beginning of the slow-closing stage, the upward rotation of the mandible slows and the jaw slowly shifts forward. During the grinding stage, the mandible is shifted forward with both toothrows in occlusion. During the opening stage, the jaw returns to its starting position. Comparison of kinematic and anatomical data on rodent mastication suggests that some dental characteristics form the most important factors regulating the masticatory pattern and consequently allow reasonably reliable prediction of rodent masticatory patterns.     

Pharyngeal mastication and food transport in the carp (Cyprinus carpio L.): A cineradiographic and electromyographic study

Cyprinids constitute the largest fish family and are characterized by their pharyngeal teeth. The masticatory mechanism is still poorly understood. The complex of structures that determine the movements of pharyngeal teeth and chewing pad in the carp (Cyprinus carpio L.) is analyzed. Activities in 16 head muscles of a free-swimming carp were recorded. X-ray cinerecordings, synchronized with electromyograms, were made of the intake, transport, mastication, and deglutition of radiopaque food pellets. Metal markers allowed a detailed movement analysis. Masticatory cycles are bilaterally synchronous and show distinct crushing and grinding patterns. Direct masticatory muscles that suspend and connect the pharyngeal bones steer and stabilize the masticatory movements. Baudelot's ligament, between skull and pectoral girdle, is applied as fulcrum, effects a crucial shift of the rotation axis of the pharyngeal jaw, and transforms crushing into grinding; simultaneous abduction lengthens the grinding stroke. Body muscles supply indirectly the power for mastication; they also appear to be regulated more distantly. The epaxial muscles lift the skull and thereby the levators of the pharyngeal bones, thus transmitting high forces to the teeth. They also stretch the levator of the bone as soon as occlusion is reached and thus optimize its production of forces during grinding. The hypaxial muscles retract the pharyngeal bones indirectly during grinding and power the teeth in sliding. The chewing pad, previously assumed to be motionless, rotates rostroventrad with the skull and intensifies grinding. Respiration and mastication are mutually related. The extensive movements of the pharyngeal bones are permitted only by the simultaneous expansion of the buccopharynx and a slide-coupling in the branchial floor. Muscular pads that line the pharynx are shown to transport food toward the teeth. The constrictor pharyngis effects deglutition. Natural food, intestinal contents, and feces of the carp were analyzed with respect to the capacity for distinct masticatory operations. During the experiments pellets, barley, and worms were fed. The carp is specialized for polyphagy and this appears to be based on the profiles of the heterodont teeth rather than on drastic changes in the two preprogrammed activity patterns. Comparison of the pharyngeal jaw system in the carp and higher teleosts emphasizes the structural design for the application of large forces in this cyprinid.     

Mandibular movement and muscle activity during mastication in the guinea pig (Cavia porcellus)

Optoelectronic analysis of mandibular movement and electromyography (EMG) of masticatory muscles in Cavia porcellus indicate bilateral, unilateral, and gnawing cycles. During bilateral and unilateral cycles, the mandibular tip moves forward, lateral, and down during the lingual phase of the power stroke to bring the teeth into occlusion. EMG activity is generally asymmetric, with the exception of activity of the temporalis muscle during bilateral cycles. During gnawing cycles, the mandible moves in an anteroposterior direction that is opposite that during bilateral and unilateral chew cycles. Bilateral and unilateral cycles of pellets were significantly longer than carrot. With the exception of the width of bilateral cycles, the magnitude of cycle width, length, and height during the mastication of carrots was greater than that during the mastication of pellets. Significant differences exist between EMG durations during mastication of pellets and carrots. The lateral pterygoid displays continuous activity during gnawing cycles. Significant differences also exist in the durations of EMG activity between the working and balancing side during all three cycle types. High level activity of balancing side temporalis and anterior belly of digastric (ABD) during bilateral cycles occurs during rotation and depression of the mandible during the power stroke. The temporalis apparently provides a ?braking”? or compensatory role during closing and power strokes. Differences between Cavia masticatory patterns and those shown by Rattus and Mesocricetus are apparently due to differences in dental morphology, occlusal relationships, and, possibly, the poorly developed temporalis in Cavia. The large number and wide diversity of rodent groups afford students of mammalian mastication an opportunity to investigate and compare different masticatory specializations.     

Mandibular biomechanics and temporomandibular joint function in primates.

There is disagreement as to whether the mandibular condyles are stress-bearing or stress-free during mastication. In support of alternative models, analogies have been drawn with Class III levers, links, and couple systems. Physiological data are reviewed which indicate that maximum masticatory forces are generated when maxillary and mandibular teeth are in contact, and that this phase lasts for over 100 msec during many chewing strokes. During this period, the mandible can be modeled as a beam with multiple supports. Equations of simple beam theory suggest that large condylar reaction forces are present during mastication. With unilateral molar biting in man, the total condylar reaction force may be over 75% of the bite force. Analysis of a frontal projection demonstrates that up to 80% of the total condylar reaction force is borne by the contralateral (balancing side) condyle during unilateral molar biting. A comparison of human, chimpanzee (P. troglodytes), spider monkey (A. belzebuth), and macaque (Macaca sp.) morphology indicates that the frugivorous chimpanzee and spider monkey have a relatively lower condylar reaction force than the omnivorous macaque or man during molar biting. The percentage reaction force during incisal biting is lower in man than in the other primates, and lower in the frugivorous primates than in the macaque.     

Mandibular function in Galago crassicaudatus and Macaca fascicularis: an in vivo approach to stress analysis of the mandible.

Single-element and/or rosette strain gages were bonded to mandibular cortical bone in Galago crassicaudatus and Macaca fascicularis. Five galago and eleven macaque bone strain experiments were performed and analyzed. In vivo bone strain was recorded from the lateral surface of the mandibular corpus below the postcanine tooth row during transducer biting and during mastication and ingestion of food objects. In macaques and galagos, the mandibular corpus on the balancing side is primarily bent in the sagittal plane during mastication and is both twisted about its long axis and bent in the sagittal plane during transducer biting. On the working side, it is primarily twisted about its long axis and directly sheared perpendicular to its long axis, and portions of it are bent in the sagittal plane during mastication and molar transducer biting. In macaques, the mandibular corpus on each side is primarily bent in the sagittal plane and twisted during incisal transducer biting and ingestion of food objects, and it is transversely bent and slightly twisted during jaw opening. Since galagos usually refused to bite the transducer or food objects with their incisors, an adequate characterization of mandibular stress patterns during these behaviors was not possible. In galagos the mandibular corpus experiences very little transverse bending stress during jaw opening, perhaps in part due to its unfused mandibular symphysis. Marked differences in the patterns of mandibular bone strain were present between galagos and macaques during the masticatory power stroke and during transducer biting. Galagos consistently had much more strain on the working side of the mandibular corpus than on the balancing side. These experiments support the hypothesis that galagos, in contrast to macaques, employ a larger amount of working-side muscle force relative to the balancing-side muscle force during unilateral biting and mastication, and that the fused mandibular symphysis is an adaption to use a maximal amount of balancing-side muscle force during unilateral biting and mastication. These experiments also demonstrate the effects that rosette position, bite force magnitudes, and types of food eaten have on recorded mandibular strain patterns.     

The depth of the lingual fossa in permanent incisors of Norwegians. II. Differences between central and lateral incisors correlations, side asymmetry and variability

The depth of the lingual fossa in permanent incisors of Norwegians (plaster casts and extracted teeth) was studied. In the plaster casts the depth of the lingual fossa in the right side incisors was (in mm): I,sup=0.51,I(2)sup= 0.30, I(1)inf =0.07 and I (2)inf =0.08. For 1(1)sup significant bilateral asymmetry was found (p<0.00l). All incisors were positively correlated in the depth of the lingual fossa, mandibular higher than maxillary. In both jaws centrals were better correlated across the midline than laterals, and centrals to laterals were less correlated than centrals to centrals and laterals to laterals. Interjaw correlations of 1(1)sup were higher than interjaw correlations with I(2)sup. Dental field theory is confirmed: The upper lateral and lower central were the most variable incisors in each jaw for lingual fossa depth. The values for this trait in Norwegians are within the Caucasoid range.     

Mandibular movements of the albino rat during feeding

Jaw movements of albino rats during biting and mastication of relatively hard food were recorded by means of conventional and X-ray cinematography. Mandibular kinetics have been analysed in the context of passive mechanical limits imposed by jaw morphology, particularly of the joints, and by the food itself. Movements have been described in terms of degrees of gape, condylar translation and horizontal rotation of the rami about the symphysis. During biting the condyle remains in the anterior two-thirds of the fossa, moves forward as the jaw opens and the converse. The rami usually spread well apart; the lower incisors are usually approximated. Incised food particles are transported toward the molars by means of coordinated jaw and tongue movements. The prominent palatal rugae of the diastemal region abet this process. In the power stroke of mastication, the mandible shifts forward as the lower toothrows move a little inward; the condyles occupy the posterior two-thirds of the fossa. All movements seen were bilaterally symmetrical. Simultaneous chewing occurred on both sides. It is suggested that the lingual components in the primarily anterior power stroke enhance grinding efficiency. A movable symphysis appears to be of critical importance in facilitating this type of mastication.     

Some dental traits of Diaguitas Indian skulls

Dental characteristics were studied on 60 skulls that belong to a population of Diaguitas Indians of approximately the Tenth Century. Mesiodistal crown diameters of permanent teeth were as follows: central incisors (8.77 mm), lateral incisors (7.23 mm), canines (8.40 mm), first maxillary molars (10.77 mm), second maxillary molars (10.71 mm), first mandibular molars (11.13 mm), and second mandibular molars (10.17 mm). Also determined was the frequency of shovel shaped incisors (80.30%), groove and cusp patterns of mandibular molars (Y5 73.40%), groove and cusp patterns of maxillary molars (H4 87.25%), and mesiopalatal version of maxillary incisors (66.20%). No skull showed Carabelli's cusp. The findings were compared with those for different populations past and living. The results suggest that the affiliation of the population analyzed was mongoloid.     

Functional and phylogenetic significance of integrated growth and form in occluding monkey canine teeth (Alouatta caraya and Macaca mulatta)

Crown-root lengths in paired apposing, functionally interacting monkey canine teeth (Alouatta caraya and Macaca mulatta) are highly correlated throughout their concurrent development. Regression is rectilinear and growth pattern accretional. The differential growth rate is not significantly different in the sexes within each species during concurrent tooth pair development. These integrated morphological characteristics are adaptations to functional needs imposed by jaw anatomy and masticatory dynamics. Divergence from rectilinearity occurs in the mature male Macaca mulatta with the continued growth of the maxillary canine fang after cessation of growth of the apposing mandibular canine tooth. This altered tooth pair crown-root length relationship is associated with the subordination of mastication in these predominantly piercing and slashing teeth. Species differences in regression are significant and afford insight into possible preadaptive factors determining divergent paths in the evolution of canine tooth sexual dimorphism.     

Precise chronology of differentiation of developing human primary dentition

While correlation of developmental stage with embryonic age of the human primary dentition has been well documented, the available information regarding the differentiation timing of the primary teeth was largely based on the observation of initial mineralization and varies significantly. In this study, we aimed to document precise differentiation timing of the developing human primary dentition. We systematically examined the expression of odontogenic differentiation markers along with the formation of mineralized tissue in each developing maxillary and mandibular teeth from human embryos with well-defined embryonic age. We show that, despite that all primary teeth initiate development at the same time, odontogenic differentiation begins in the maxillary incisors at the 15th week and in the mandibular incisors at the 16th week of gestation, followed by the canine, the first primary premolar, and the second primary premolar at a week interval sequentially. Despite that the mandibular primary incisors erupt earlier than the maxillary incisors, this distal to proximal sequential differentiation of the human primary dentition coincides in general with the sequence of tooth eruption. Our results provide an accurate chronology of odontogenic differentiation of the developing human primary dentition, which could be used as reference for future studies of human tooth development.     

Morphological features of Jat dentition

Observations on morphological characters of milk and permanent teeth, based on 648 pairs of dental casts of 356 male and 292 female Jat children of Haryana (India) are reported. Deciduous teeth show high frequencies of bilateral winging of maxillary central incisor, Carabelli's cusp of maxillary second molar, and deflecting wrinkle of mandibular second molar. Reduction of maxillary molar cusps is more marked in males than in females. Y pattern is very common in deciduous molars. Permanent teeth have high frequencies of grooved cingulum of incisors, cingular nodule of lateral incisors and canines, and distal accessary ridge of canines. Low frequencies of Carabelli's cusp and winging are also common. The tendency towards faintly developed shovelling in milk incisors occurs more often than in the permanent teeth.     

The depth of the lingual fossa in permanent incisors of Norwegians. I. Method of measurement, statistical distribution and sex dimorphism

The depth of the incisor lingual fossa in permanent extracted incisors and plaster casts of Norwegians was examined. It was shown that plaster casts are well suited for measurements of lingual fossa depth, and that the measurements can be performed with great accuracy. Skewness values showed the symmetry of the distribution to decrease with decreasing mean lingual fossa depth. Kurtosis was found small in maxillary incisors, in mandibular outside the limits for normal theory. The distribution of the depth of the lingual fossa cannot generally be described as normal. No sex differences were found. The inheritance of this trait in Norwegians is probably not sex linked.     

Pulp sensibility test in elderly patients

doi: 10.1111/j.1741‐2358.2012.00623.x
Pulp sensibility test in elderly patients Background: The ageing process transforms the histological composition of the dental pulp and may affect the response to pulp sensibility tests. Objectives: The aim of this study was to assess the influence of age on pulp response time and on pain intensity. Material and methods: Fifty elderly patients and 50 young patients were selected. Different classes of teeth were evaluated. The pulp sensibility test was performed with a refrigerant spray. The pulp response time was measured in seconds and the pain intensity was assessed by visual analogue scale. Results: The Spearman coefficient was calculated and detect a positive correlation between age and pulp response time for maxillary incisors, premolars, mandibular incisors, and mean (p < 0.05). On the contrary, there was a negative correlation between age and pain intensity for maxillary incisors, mandibular incisors, and mean (p < 0.05). Also, the results of elderly and young groups were compared by Mann–Whitney test. Significant difference was noted regarding the pulp response time for maxillary incisors, premolars, mandibular incisors, and mean (p < 0.05). Significant difference was detected regarding the pain intensity for mandibular incisors only (p < 0.05). Conclusions: Pulp response time increases when people get older while pain intensity decreases. There were variations among the classes of teeth.