A study of sutural bones in Anatolian-Ottoman skulls

In this study, a total of 302 adult Anatolian-Ottoman skulls were classified into three morphological forms (dolichocephalic, mesocephalic, brachycephalic), and were examined in order to find the incidence of sutural bones in each forms. In addition, the cranial capacity was measured in the skulls with and without sutural bones. Comparison of the incidence of sutural bones in each form of the skulls, and cranial capacity in skulls with and without sutural bones showed no significant difference. In most populations, the average measure of difference between Anatolian-Ottoman and the others was statistically significant. In conclusion, the incidence of sutural bones is well suited for comperative studies as an anthropological marker or an indicator of population distance. This study was presented in the 3rd National Anatomy Congress (6–9 Sept 1995) Izmir, Türkiye.     

Sutural bone frequency in synostotic rabbit crania

This study tests the hypothesis that crania with synostosed sutures will have a significantly higher incidence of calvarial sutural bones than normal crania. Sutural bones were counted in seven calvarial sutures and compared among four groups of adult New Zealand white rabbit skulls: normal in-colony (NI) controls (N = 14), normal out-colony (NO) controls (N = 12), skulls with familial delayed onset (DO) coronal synostosis (N = 25), and skulls with experimentally immobilized coronal sutures (EI) (N = 20). Comparisons among groups were made with a Kruskal-Wallis one-way ANOVA and between groups with a Mann-Whitney U-test, using a Bonferroni correction for multiple comparisons. Significant differences (P > 0.05) were noted only in the coronal and sagittal sutures, with EI crania having the greatest number of coronal sutural bones; between group differences were undetectable for sagittal sutural bones. A post hoc two-sample binomial test for equal proportions showed that the distribution of coronal sutural bones among individuals across groups was even, while the distribution of sagittal sutural bones was significantly higher in EI crania. These results suggest that altered sutural forces of the calvaria contribute to an increased occurrence of sutural bones. However, the influence of inheritance on increased occurrence of sutural bones cannot be discounted, as reflected in the equivalent number of individuals across groups that possessed coronal sutural bones. Am J Phys Anthropol 102:555–563, 1997. © 1997 Wiley-Liss, Inc.     

A study of sutural bones in Gujarati (Indian) crania

370 adult crania were examined to find the incidence of sutural bones in Gujarati (Indian) crania and to compare it with other populations to establish the distance between them. The mean measure of difference between Indian and other populations was statistically significant. Comparison of cranial capacity in skulls with and without sutural bones showed no significant difference, and this is interpreted as indicating that sutural bones are not formed secondary to stress.     

A study of sutural bones in different morphological forms of skulls

117 adult human skulls were classified for three morphological forms, i.e. dolichocephalic, mesocephalic and brachycephalic, and were examined for the presence of sutural bones in each form. Sutural bones occur in each forms of the skulls with no statistically significant differences. This finding is interpreted as indicating that sutural bones are not formed secondary to stress, otherwise the incidence of the sutural bones would have been differed in different morphological forms of skulls.     

Sutural complexity in artificially deformed human (Homo sapiens) crania.

The pattern of complexity of cranial sutures is highly variable both among and within species. Intentional cranial vault deformation in human populations provides a controlled natural experiment by which we were able to quantify aspects of sutural complexity and examine the relationship between sutural patterns and mechanical loading. Measures of sutural complexity (interdigitation, number, and size of sutural bones) were quantified from digitized tracings of 13 sutures and compared among three groups of crania (n = 70) from pre-European contact Peru. These groups represent sample populations deformed in 1) anteroposterior (AP) and 2) circumferential (C) directions and 3) an undeformed population. Intergroup comparisons show few differences in degree or asymmetry of sutural interdigitation. In the few comparisons which show differences, the C group is always more interdigitated than the other two while the AP group has more sutural bones. The sutures surrounding the temporal bone (sphenotemporal, occipitotemporal, and temporoparietal) most frequently show significant differences among groups. These differences are related to the more extreme binding of C type deformation and are consistent with hypothesized increases in tension at coronally oriented sutures in this group. The larger number of sutural bones in the AP group is consistent with the general broadening of the cranium in this group and with experimental evidence indicating the development of ossicles in areas of tension. We suggest that so few changes in sutural complexity occurred either because the magnitude of the growth vectors, unlike their direction, is not substantially altered or because mechanisms other than sutural growth modification are responsible for producing the altered vault shapes. In addition, the presence of fontanelles in the infant skulls during binding and the static nature of the binding may have contributed to the similarity in complexity among groups.     

Remodeling of the sagittal suture in osteopetrotic (op/op) mice associated with cranial flat bone growth.

It is well known that cranial flat bone experiences growth and development at the sutural interface, which is regarded as a neutral zone to control mechanical stimuli. In osteopetrotic (op/op) mice, meanwhile, cranial deformation is produced by the deficiency of osteoclasts and the subsequent defect of bone resorption. It would be a reasonable assumption that such disturbance in bone remodeling affects sutural modification and the relevant cranial flat bone development. The present study was thus conducted to examine histological features of the sagittal sutures in op/op mice, with special reference to the relevant bone remodeling. The sagittal sutures in 10-, 15-, 30-, and 60-day-old normal and op/op mice were observed microscopically. Furthermore, osteoclastic activity was evaluated on the sections stained with tartrate-resistant acid phosphatase (TRAP). The sutures of 15-day-old op/op mice showed stenosis and synostosis, and less-developed collagen fibers associated with an irregular arrangement of fibroblasts, whereas these changes were rarely found in normal mice. Osteoclasts were hardly detected in the parietal bones around the sutures of op/op mice, although the number was numerous in normal mice. These results emphasize that congenital deficiency in osteoclast produces unbalanced bone remodeling at the sutural interface and on the surfaces of the cranial bones, which is assumed to be closely related to cranial bone deformity in op/op mice.     

Artificial cranial deformation and the increased complexity of the lambdoid suture

Studies examining an association between artificial cranial deformation and the presence of wormian bones in the lambdoid suture have been inconclusive. Cranial deformation, however, does not seem to have a direct effect of increasing the sutural complexity of the pars lambdica of the lambdoid suture and also increasing the mean number of lambdoidal wormian bones, given their presence.     

A note on craniofacial sutural growth

The paper presents and discusses some features of sutural structures. Fibre orientation in sutures seems to be quite variable and associated with minute local growth phenomena. Trabecular patterns in bones, reflecting growth, appear to support the idea of the outside determination of growth. The bevelled and interdigitated structures seen in many sutures may be interpreted as an expedient solution to the problem of fast growth.     

The sutural pattern of skull-roof bones in Lower Permian Discosauriscus austriacus from Moravia

Sutures between ornamented bones of Discosauriscus austriacus are mostly simple, but there are also more complicated, rarely serrated, sutures between some bones. In small individuals, the sutures are simple, but the same sutures also occur in the largest specimens. The character of the sutures and the incomplete ossification of bones around the pineal foramen indicate the larva type of organization of Discosauriscus The fenestra between premaxillaries and nasals appears to be absent. In the majority of specimens, a squamosal-intertemporal sutural contact is present, althought it is sometimes reduced and in a few cases interrupted by a postorbital and supratemporal contact Therefore the character 'intertemporal-squamosal suture present or absent' cannot be used in this rigorous sense for testing the relationships of early tetrapods. The configuration of the suture between both parietals in osteolepiforms, Discosauriscus , and various early amphibians and reptiles indicates that the bones enclosing the pineal foramen in osteolepifonns are frontals. *** D iscosauriscus . Seymouriamorpha, Lower Permian tetrapod, skull exoskeleton, sutures.     

Studies on the skull of the Indian sisorid catfish, Erethistes pussilus

The skull of Erethistes pussilus is described in detail. The general disposition of the bones corresponds to the siluroid pattern. Among the siluroid fishes, E. pussilus approaches the advanced forms in certain features such as obliteration of myodomic space, edentulous palate, absence of entopterygoids and supratemporals, intimate sutural articulation of posttemporals and complex vertebra with the cranium, diminished cranial cavity and loss of sutural articulation among the palatopterygoquadrate elements. In certain characters like the hyomandibula exclusively supported from the sphenotic, solitary hypohyal on each hyoid cornu, absence of interhyals, reduced orbits, edentulous vomer, small gape of mouth, toothless ectopterygoid and in the small number of branchiostegals, E. pussilus stands specialized alone among the catfishes. A diagnosis of the salient cranial characters of the fish is given and its relationship discussed.     

Studies on the skull of the Indian sisorid catfish, Erethistes pussilus

The skull of Erethistes pussilus is described in detail. The general disposition of the bones corresponds to the siluroid pattern. Among the siluroid fishes, E. pussilus approaches the advanced forms in certain features such as obliteration of myodomic space, edentulous palate, absence of entopterygoids and supratemporals, intimate sutural articulation of posttemporals and complex vertebra with the cranium, diminished cranial cavity and loss of sutural articulation among the palatopterygoquadrate elements. In certain characters like the hyomandibula exclusively supported from the sphenotic, solitary hypohyal on each hyoid cornu, absence of interhyals, reduced orbits, edentulous vomer, small gape of mouth, toothless ectopterygoid and in the small number of branchiostegals, E. pussilus stands specialized alone among the catfishes. A diagnosis of the salient cranial characters of the fish is given and its relationship discussed.     

Sutural expansion osteogenesis for management of the bony-tissue defect in cleft palate repair: experimental studies in dogs

A series of experimental studies on sutural expansion osteogenesis for management of the bony-tissue defect in cleft palate repair was performed between 1995 and 1997. Forty-five young dogs in weaning were used in four experiments that were divided into two parts. Part I probed the possibility of closing the surgically constructed hard palate cleft not only with mucoperiosteum but also with bony tissue by the technique of sutural expansion of lateral palatine sutures. Part II explored the possibility of pushing the palatine bone posteriorly and advancing the maxillary segment anteriorly by transverse palatine suture expansion. In Part I, a ring-shaped suture expander made of nickel-titanium shape memory alloy was used to expand the lateral suture of palatine bones. Expansion forces of 200 G, 360 G, and 480 G were used for the first experiment. A force of 360 G was chosen for two other experiments; this force is equivalent to the distraction rate of 0.5 mm per day of a jackscrew device. The ring-shaped suture expander was opened and its two feet were fixed in the medial sides of residual horizontal plates of the palatine bones immediately after a hard palate cleft was constructed surgically under endotracheal general anesthesia. At the eighth postoperative day, under the traction of 360 G, the two sides of the 8-mm-wide hard palate cleft were brought into contact with each other, and 8 or 9 days later the closed palatal cleft had healed completely with mucosal tissue. This experiment was repeated twice and yielded the same results. Sutural expansion osteogenesis was evaluated physically, fluorescently, histologically, and ultrastructurally to examine the deposition of the regenerated bone in the suture areas. Additionally, the influence of sutural expansion osteogenesis of the palatal bones on other facial bones was also studied cephalometrically. In Part II, a bow-shaped suture expander made of nickel-titanium shape memory alloy was applied to expand either the left or the right side of the transverse palatal suture of each of the experimental dogs. At the postoperative week 4 to 6, the maxillary segment was moved forward 5 to 6 mm on the expanded side, and the palatal bone was pushed backward 5 mm. The changes of bone position were assessed radiographically and cephalometrically. Tissue response of circum-maxillary sutures was examined histologically. These experiments led to the following conclusions: (1) Bony closure of the surgically constructed hard palate cleft with a ring-shaped suture expander made of nickel-titanium shape memory alloy is possible. (2) Anterior advancement of the maxillary segment and posterior lengthening of the hard palate using a bow-shaped suture expander made of nickel-titanium shape memory alloy applied at the palatomaxillary suture (transverse palatal suture) of the hard palate are also possible. Thus, in humans, a new approach for cleft palate repair may be a worthwhile investigation.     

Mechanical properties of cranial sutures

Many bones in mammalian skulls are linked together by cranial sutures, connective tissue joints that are morphologically variable and show different levels of interdigitation among and within species. The goal of this investigation was to determine whether sections of skull with cranial sutures have different mechanical properties than adjacent sections without sutures, and if these properties are enhanced with increased interdigitation. To test these hypotheses, bending strength and impact energy absorption were measured for samples of goat (Capra hircus) cranial bone without sutures and with sutures of different degrees of interdigitation. Bending strength was measured under both dynamic (9.7 mm displacement s-1) and relatively static (0.8 mm s-1) conditions, and at either speed, increased sutural interdigitation provided increased strength during three-point bending. However, except for very highly interdigitated sutures loaded slowly, sutures were not as strong in bending as bone. In contrast, sutures absorbed from 16% to 100% more energy per unit volume during impact loading than did bone. This five-fold increase in energy absorption by the sutures was significantly correlated with increased sutural interdigitation.     

Effects of different kinds of cranial deformation on the incidence of wormian bones

Researchers have debated whether the presence and frequency of wormian bones (sutural bones, supernumerary bones, and ossicles) are attributable to genetic factors, environmental factors, or both. This research examines the effects of many different kinds of cranial deformation on the incidence of wormian bones. A sample of 127 deformed and undeformed crania from New World archaeological sites was examined. An undeformed cranial sample (n=35) was compared to the following cranially deformed groups: 1) occipital, 2) lambdoid, 3) annular, 4) fronto-vertico-occipital, 5) parallelo-fronto-occipital, and 6) sagittal synostosis. Three levels of degree of cultural cranial deformation were qualitatively determined. Type and number of wormian bones along each major suture were recorded for each cranium. Group means were analyzed using Kruskal-Wallis one-way ANOVA statistical tests to test the null hypothesis that cranial deformation does not have an effect on wormian bone incidence. Results indicate that all forms of cranial deformation affect the frequency of some types of wormian bones. In particular, all cranially deformed groups exhibited significantly greater frequencies of lambdoid ossicles. Apical, parieto-mastoid, and occipito-mastoid wormian bones also appeared with greater frequency in some groups of culturally deformed crania. Further, varying degrees of cultural deformation all had more lambdoid wormian bones than the undeformed group. These results suggest that wormian bone development in posteriorly placed sutures may be affected more by environmental forces than are their anteriorly placed counterparts.     

The morphology and relationships of the Carboniferous amphibian Eoherpeton watsoni Panchen

The oldest recorded anthracosaur amphibian Eoherpeton watsoni Panchen, from localities in the Visean and Namurian of the Scottish Carboniferous, is described. It lacks a distinct otic notch, and reconstruction of the position of cranial ligaments and muscles suggest that a tympanum was never developed. On the basis of these observations it is concluded that arguments used to refute a relationship between anthracosaurs and amniotes, based on apparent differences in the morphology of their otic regions, are invalid. The order Anthracosauria is considered to be a monophyletic group characterized by the development of a sutural connection between the tabular and parietal bones on a skull table which includes both the intertemporal and supratemporal as well as the tabular. It is divided into two suborders: Seymouriamorpha characterized by a sutural connection between the squamosal and intertemporal and the presence of a lateral otic tube, and Anthracosauroideae characterized by the absence of post-temporal fossae. The Discosauriscidae, Kotlassiidae and Seymouriidae are included in the Seymouriamorpha, and the Eoherpetontidae, Gephyrostegidae and Embolomeri comprise the Anthracosauroideae. The Proterogyrinidae are considered the most primitive family of embolomeres. A new phylogeny of Amphibia is presented. The old groupings of Labyrinthodontia, Lepospondyli and Lissamphibia are rejected and Amphibia is divided, on the basis of differences in morphology of the neurocranium and its relationship with the surrounding bones of the skull, into two major groups, the first including the Ichthyostcgalia, Temnospondyli, Microsauria and the extant Anura, Apoda and Urodela, while the Aistopoda, Nectridea, Palaeostegalia, Loxommatoidea, Anthracosauria and Diadectomorpha, together with the Amniota, form the second. Similarities in the dentition of the palaeostegalian Crassigyrinus and loxommatoids suggest the two taxa are sister-groups, but the immediate relationships of anthracosaurs remain indeterminate and they here form an unresolved trichotomy with diadectomorphs and amniotes.     

Das coronoid der paulchoffatiidae (multituberculata; ober-jura)

For the first time the presence of a rudimentary coronoid bone in the mandible can be proved, among the Kimmeridgian Paulchoffatiidae of the Guimarota coal mine near Leiria/Portugal. In 3 specimens remains of the bone in situ are present; in others only its sutural surface is preserved. The coronoid is a small bone placed immediately posteriorly to the second molar, variable in outline. In shape and position it is more similar to the coronoid of the contemporaneous Docodonta —Haldanodon — than to that of the also contemporaneous Eupantotheria, in which it is larger and situated higher on the coronoid process. Other accessorial bones, the sulcus mylohyoideus and the Meckelian cartilage are not present. With that it is proved that in all Mammalian orders known from the Guimarota coal mine — Docodonta, Eupantotheria, Multituberculata — accessorial bones in the lower jaw persist in a more or less degree, and it seems probable that in Kimmeridgian time the presence of such reptilian bones is the normal condition in mammals.     

Cell fate specification during calvarial bone and suture development

In this study we have addressed the fundamental question of what cellular mechanisms control the growth of the calvarial bones and conversely, what is the fate of the sutural mesenchymal cells when calvarial bones approximate to form a suture. There is evidence that the size of the osteoprogenitor cell population determines the rate of calvarial bone growth. In calvarial cultures we reduced osteoprogenitor cell proliferation; however, we did not observe a reduction in the growth of parietal bone to the same degree. This discrepancy prompted us to study whether suture mesenchymal cells participate in the growth of the parietal bones. We found that mesenchymal cells adjacent to the osteogenic fronts of the parietal bones could differentiate towards the osteoblastic lineage and could become incorporated into the growing bone. Conversely, mid-suture mesenchymal cells did not become incorporated into the bone and remained undifferentiated. Thus mesenchymal cells have different fate depending on their position within the suture. In this study we show that continued proliferation of osteoprogenitors in the osteogenic fronts is the main mechanism for calvarial bone growth, but importantly, we show that suture mesenchyme cells can contribute to calvarial bone growth. These findings help us understand the mechanisms of intramembranous ossification in general, which occurs not only during cranial and facial bone development but also in the surface periosteum of most bones during modeling and remodeling.     

Jaw muscles and the skull in mammals: the biomechanics of mastication.

Among non-mammalian vertebrates, rigid skulls with tight sutural junctions are associated with high levels of cranial loading. The rigid skulls of mammals presumably act to resist the stresses of mastication. The pig, Sus scrofa, is a generalized ungulate with a diet rich in resistant foods. This report synthesizes previous work using strain gages bonded to the bones and sutures of the braincase, zygomatic arch, jaw joint, and mandible with new studies on the maxilla. Strains were recorded during unrestrained mastication and/or in anesthetized pigs during muscle stimulation. Bone strains were 100-1000 micro epsilon, except in the braincase, but sutural strains were higher, regardless of region. Strain regimes were specific to different regions, indicating that theoretical treatment of the skull as a unitary structure is probably incorrect. Muscle contraction, especially the masseter, caused strain patterns by four mechanisms: (1) direct loading of muscle attachment areas; (2) a compressive reaction force at the jaw joint; (3) bite force loading on the snout and mandible; and (4) movement causing new points of contact between mandible and cranium. Some expected patterns of loading were not seen. Most notably, strains did not differ for right and left chewing, perhaps because pigs have bilateral occlusion and masseter activity.     

Skeletal growth and chondroid tissue

Membranous and endochondral ossification processes are insufficient to describe all the aspects observed in the growing skeleton. The presence of chondroid tissue that we have identified by means of all modern histological techniques, including those able to detect the different types of collagen, has also to be explained. Present in the mandibular symphysis of either the human or cat fetuses, chondroid tissue has also been observed in the other parts of the mandible, in the sutural areas of the skull and in all the bones of both axial and appendicular skeleton. The differentiation of the mesenchyme into chondroid tissue could probably be related with mechanical forces exerted simultaneously in opposite directions or with a transient ischemia.