Christopher J. Vinyard’s research while affiliated with Ohio University and other places

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Publications (176)


Three‐dimensional reconstruction of the specimen M90628 (Procavia capensis). (a) Cross‐section of the tusks (incisors), the white arrow points toward the dorsal side. (b) Coronal section of the dp4 and P4. (c) Sagittal section of the dp4–P4 and M1–M2. (d) Three‐dimensional reconstruction of the same specimen (Lateral view). (e) Sagittal section of the left dental raw. (f) Cross‐section of the tusks of the adult specimen H5101A. (g) Sagittal section of the dental row (same specimen as f). In all sagittal view, left side = rostral. Scale = 1 mm.
The tusk (I1) and first deciduous (dp1) and replacement premolar (P1) in the subadult hyrax. The tusk housed within the premaxilla (PMx) at the same level as the first premolar are shown in microcyte (a) and histology (b). (c) P1 has inner enamel epithelium (IEE) adjacent to the enamel space (ES) on buccal and lingual sides, whereas the occlusal side is covered by reduced enamel epithelium (REE). (d, e) The IEE is high columnar epithelium along much of the crown, diminishing in height near the cervical region. (f) The dentin (D) stains deeply red with Gomori trichrome stain, as contrasted with bright green predentin (PD). Scale bars: a, b, 1 mm; c–f, 30 μm.
The tusk (I1) and second deciduous (dp2) and replacement premolar (P2) in the subadult hyrax. The tusk housed within the premaxilla (PMx) at the same level as the first premolar are shown in microCT (a) and histology (b). (c) Magnified view of the tusk crypt (see box in (b) for location), showing the internal enamel epithelium (IEE) and a thin fragment of enamel. (e, f) Rostral to caudal series of the tusk; € is rostral to the premolar, and (f) is at the same level as P3/dp3. Note the greatly increased dentin thickness from caudal to rostral; thin enamel is detectable caudally (f), whereas an enamel space (ES) is observed at more rostral levels. (g) The wall of the tusk crypt caudally (see box in (b) for location), showing a thin shell of the PMx. (h) Low magnification view of P2, showing thick dentin and an ES to its lingual and buccal sides. A box indicates the location of the enlarged view in (i), which reveals the high columnar IEE. PL, papillary layer. Scale bars: a, b, 1 mm; c, 10 μm; d, e, 400 μm; f, 200 μm; g, 50 μm; h, 0.5 mm; i, 10 μm; all insets, 1 mm.
The fourth deciduous (dp4) and replacement premolar (P4) in the subadult hyrax, shown in microCT (a) and histology (b). The boxed region in (b) is enlarged in (c), revealing part of the pulp cavity (P) and adjacent dentin (D) and enamel. The enamel is fragmentary near the occlusal side of the crown. But closer to the cervix (d), showing an adjacent section, the enamel is intact. The internal enamel epithelium has a “picket‐fence” appearance (white arrows), indicating the presence of Tomes' processes at the apex of the ameloblasts. Scale bars: a, 1 mm; b, 0.5 mm; c, 100 μm; d, 10 μm.
A section prepared using RUNX2 immunohistochemistry (fast green counter stain), showing the replacement premolar (a‐d) and tusk (e) in the subadult hyrax. (a) This section shows the root (upper right) and part of the crown, excluding the enamel, which was destroyed during the decalcification process. (b) An enlargement of the cervical (Ce) region of the same tooth reveals few reactive cells near the crown, but sparse moderately RUNX2+ cells (arrowheads) are present adjacent to the root. (c) High magnification view of the cervical region (see box in plate (a) for location), showing RUNX2+ cells (arrowheads) near the cervical region. (d) The internal enamel epithelium (IEE) of the same tooth, but more apical to the field of view in plate (a). The IEE has numerous RUNX2+ ameloblasts (arrowheads). Note there are no RUNX2+ below the heavily fibrous inner layer of the follicle (Fo). (e) The IEE of the tusk also has numerous RUNX2+ ameloblasts (arrowheads). Insets in (b), (d), and (e) show there is no discernable non‐specific background staining in negative controls. Scale bars: a, 200 μm; b, 50 μm; c–e and all insets, 20 μm.
Prolonged or perpetual growth of replacement teeth in the rock hyrax
  • Article
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December 2024

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32 Reads

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Laura Bento Da Costa

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Sarah E. Downing

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Tusks are ever‐growing teeth present in mammals of the clade Paenungulata. Unlike the perpetually growing incisors of rodents, tusks are not used in mastication, and in at least some paenungulatans, the tusk is composed of dentin alone in adults. Few studies have provided tissue‐level information on tusks of adult paenungulatans with embedding techniques that identify epithelial and other soft tissues. In order to examine the mineralized tissues as well as the cells that form teeth, we studied a single, subadult rock hyrax (Procavia capensis) using microCT and paraffin histology with traditional staining as well as RUNX2 immunohistochemistry, and compared its teeth to scans of adult hyraxes. Three‐dimensional reconstructions from microCT volumes revealed that the tusk of this specimen is the only fully erupted replacement tooth, the first adult premolar (P1) is starting to erupt, and the first permanent molar (M1) is fully erupted, whereas all other replacement teeth and M2 remain in crypts. The tusk has a thin layer of enamel on its dorsal side; this is confirmed by histology. All deciduous premolars still possess roots that are in the process of resorption. Amelogenesis has progressed to maturation or nearly so in P1–P3. Notable histological characteristics of replacement premolars include the lack of a stellate reticulum in all except P4, and expression of RUNX2 in ameloblasts, a marker which is expressed by ameloblasts at all stages of amelogenesis. Since the pulp chambers of replacement premolars are relatively large compared to adults, a lengthy time in crypts may be important for dentin production. The results confirm that the hyrax has thin enamel on tusks, supporting the hypothesis that enamel is of limited importance for non‐feeding behaviors.

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Figure 1. Figure of a wild baboon (Papio hamadryas) male engaged in a canine gape display. Photo courtesy of L. Hlusko and licensed on Wikimedia Commons (CC-BY-SA-4.0). File:Papio (hamadryas) anubis baboon, Ngorongoro National Park, Tanzania, 2014.png (2022, August 2). Wikimedia Commons. Retrieved August 20, 2023 from https://commons.wikimedia.org/wiki/File:Papio_(hamadryas)_anubis_baboon,_Ngorongoro_National_Park,_Tanzania,_2014.png&oldid=679744106).
Figure 2. The three datasets used in this analysis. Refer to SOM Table S1 for means and standard deviations for all species/sexes and variables used in this study. Abbreviations: F = females; M = males; TMJ = temporomandibular joint. a) Data from Hylander (2013). Numbers represent samples from living vs. museum specimens (living/museum). b) Data from Terhune et al. (2015), Taylor et al., 2018, and Taylor (this paper). c) Data from Terhune (2010). d) Terhune data are for Trachypithecus obscurus. e) Terhune data are for Colobus polykomos. f) Terhune data are for Lophocebus albigena. g) Terhune data are for Cercocebus torquatus, while in the Hylander dataset this species is listed only as Cercocebus atys. h) Hylander data are for Cercopithecus diana. Consensus phylogeny of all 32 species included in the analysis downloaded from the 10kTrees website (10kTrees v. 3, http://10ktrees.fas.harvard.edu/; Arnold et al., 2010).
Figure 6. Bivariate plots of the relationships between jaw length (top), maximum gape (middle), canine height (bottom), and either superficial masseter (A–C) or temporalis fiber length (D–F). All variables were measured in millimeters and natural log (Ln) transformed for analysis. All correlations are significant for males (p < 0.05) but only the correlation between canine height and temporalis fiber length (F) is significant for females (p = 0.002). See Table 3 for details. Abbreviations: Caet = Chlorocebus aethiops; Caty = Cercocebus atys; Cgal = Cercocebus galeritus; Ctor = Cercocebus torquatus; Cgue = Colobus guereza; Cmit = Cercopithecus mitis; CnicF = Cercopithecus nictitans; Epat = Erythrocebus patas; Mfas = Macaca fascicularis; Mmul = Macaca mulatta; Mleu = Mandrillus leucophaeus; Msph = Mandrillus sphinx; Mtal = Miopithecus talapoin; Nlar = Nasalis larvatus; Panu = Papio anubis; Pham = Papio hamadryas; Pnem = Pygathrix nemaeus; Tgel = Theropithecus gelada; Tfra = Trachypithecus francoisi.
Jaw-muscle fiber architecture and skull form facilitate relatively wide jaw gapes in male cercopithecoid monkeys

November 2024

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34 Reads

Journal of Human Evolution

In primates and other mammals, the capacity to generate a wide maximum jaw gape is an important performance variable related to both feeding and nonfeeding oral behaviors, such as canine gape display and clearing the canines for use as weapons during aggressive encounters. Across sexually dimorphic catarrhine primates, gape is significantly correlated with canine height and with musculoskeletal features that facilitate wide gapes. Given the importance of canine gape behaviors in males as part of intrasexual competition for females, functional relationships between gape, canine height, and musculoskeletal morphology can be predicted to differ between the sexes. We test this hypothesis by investigating sex-specific relationships among these variables in a maximum sample of 32 cercopithecoid species. Using phylogenetic least squares regression, we found that, of 18 predicted relationships, 16/18 (89%) were significant in males while only six (33%) were significant in females. Moreover, 15/18 correlations were higher—10/18 significantly higher—in males compared with females. Males, but not females, showed strong and significant positive allometry of fiber lengths, indicating that increase in male jaw length is accompanied by allometric increases in the capacity for muscle stretch. While males and females showed significant negative allometry for muscle leverage, only males showed significant negative allometry of muscle leverage relative to jaw gape and canine height. Collectively, these results provide support for the hypothesis that as selection acted to increase relative canine height in male cercopithecoids, one change was an allometric increase in relative maximum jaw gape, along with allometric increases in musculoskeletal morphologies that facilitate gape. Lastly, if gape and canine display/clearance are key targets of selection on masticatory morphology in male cercopithecoids, then cercopithecoid monkeys like macaques, baboons, and sooty mangabeys may have diminished utility as models for drawing paleobiological inferences from musculoskeletal morphology about feeding behavior and diet in fossil hominins.


Concerns of osteopathic medical students during the COVID-19 pandemic

May 2024

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15 Reads

Objectives This study aims to quantify the areas of most concern in medical students in relation to their residency application in the setting of the COVID-19 pandemic and to identify risk factors for all that cause concern and specific areas of concern in a population with well-established high rates of anxiety at baseline. The COVID-19 pandemic introduced sweeping changes to medical education that had wide-ranging effects on medical students and their applications for medical residencies. Methods In August 2020, we utilized a cross-sectional study to quantify student’s areas of concern related to residency application related to the COVID-19 pandemic. We asked participants to rate their levels of concern in 15 different aspects related to medical residency applications and the perceived impact that COVID-19 had on each. Results The survey was distributed to 984 osteopathic medical students, with 255 complete responses. The three areas of greatest impact were shadowing opportunities (4.15), volunteer opportunities (4.09), and conferencing opportunities (4.09). The most salient demographic variables were year in school, sex, and locale. Females reported higher levels of concern across all categories in the study compared to males, with statistical significance across all categories (all p<0.05, Range d=0.16 to 0.43), except for letters of recommendation and sub-internships. Conclusions The areas of most concern identified in our study were consistent with prior studies and may implicate the pressures that female medical students may feel compared to their male counterparts. The underlying cause(s) may be subject to future research.


Developmental milestones in captive Galago moholi

May 2024

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46 Reads

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1 Citation

American Journal of Primatology

Systems of the body develop in a modular manner. For example, neural development in primates is generally rapid, whereas dental development varies much more. In the present study, we examined development of the skull, teeth, and postcrania in a highly specialized leaping primate, Galago moholi . Eighteen specimens ranging from birth to adult were studied. Bones, teeth, and the cranial cavity (i.e., endocast) were reconstructed with Amira software based on microCT cross‐referenced to histology. Amira was also used to compute endocast volume (as a proxy for brain size). Reconstructions of the wrist and ankle show that ossification is complete at 1 month postnatally, consistent with the onset of leaping locomotion in this species. Endocranial volume is less than 50% of adult volume at birth, ~80% by 1 month, and has reached adult volume by 2 months postnatal age. Full deciduous dentition eruption occurs by 2 weeks, and the young are known to begin capturing and consuming arthropods on their own by 4 weeks, contemporaneous with the timing of bone and ankle ossification that accompanies successful hunting. The modular pattern of development of body systems in Galago moholi provides an interesting view of a “race” to adult morphology for some joints that are critical for specialized leaping and clinging, rapid crown mineralization to begin a transitional diet, but perhaps more prolonged reliance on nursing to support brain growth.



Bootstrapped distributions of platyrrhine species. (a) RMA slope estimates for Log10 superficial masseter fibre length (Lf) regressed on Log10 jaw length, (b) correlations for Log10 Lf and Log10 jaw length and (c) p‐values for RMA slope estimates. Small sample‐few species (SS‐FS) are shown in light gray, Large sample‐few species (LS‐FS) in dark gray and Large sample‐many species (LS‐MS) in red. Note the reduced dispersion as sample sizes increase and the major shift in average slope estimates in the ‘many species’ compared to ‘few species’ models.
Bootstrapped distributions of platyrrhine species. (a) RMA slope estimates for Log10 superficial masseter PCSA0.5 regressed on Log10 jaw length, (b) correlations for Log10 PCSA0.5 and Log10 jaw length and (c) p‐values for RMA slope estimates. Small sample‐few species (SS‐FS) are shown in light gray, Large sample‐few species (LS‐FS) in dark gray and Large sample‐many species (LS‐MS) in red. Note the reduced dispersion as sample sizes increase and the major shift in average slope estimates in the ‘many species’ compared to ‘few species’ models.
The impact of measurement technique and sampling on estimates of skeletal muscle fibre architecture

February 2024

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75 Reads

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1 Citation

Skeletal muscle fibre architecture provides important insights into performance of vertebrate locomotor and feeding behaviours. Chemical digestion and in situ sectioning of muscle bellies along their lengths to expose fibres, fibre orientation and intramuscular tendon, are two classical methods for estimating architectural variables such as fibre length (Lf) and physiological cross‐sectional area (PCSA). It has recently been proposed that Lf estimates are systematically shorter and hence less accurate using in situ sectioning. Here we addressed this hypothesis by comparing Lf estimates between the two methods for the superficial masseter and temporalis muscles in a sample of strepsirrhine and platyrrhine primates. Means or single‐specimen Lf estimates using chemical digestion were greater in 17/32 comparisons (53.13%), indicating the probability of achieving longer fibres using chemical digestion is no greater than chance in these taxonomic samples. We further explored the impact of sampling on scaling of Lf and PCSA in platyrrhines applying a bootstrapping approach. We found that sampling—both numbers of individuals within species and representation of species across the clade significantly influence scaling results of Lf and PCSA in platyrrhines. We show that intraspecific and clade sampling strategies can account for differences between previously published platyrrhine scaling studies. We suggest that differences in these two methodological approaches to assessing muscle architecture are relatively less consequential when estimating Lf and PCSA for comparative studies, whereas achieving more reliable estimates within species through larger samples and representation of the full clade space are important considerations in comparative studies of fibre architecture and scaling.



Comparing age‐ and bone‐related differences in collagen fiber orientation: A case study of bats and laboratory mice using quantitative polarized light microscopy

December 2023

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74 Reads

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1 Citation

As bones age in most mammals, they typically become more fragile. This state of bone fragility is often associated with more homogenous collagen fiber orientations (CFO). Unlike most mammals, bats maintain mechanically competent bone throughout their lifespans, but little is known of positional and age‐related changes in CFO within wing bones. This study tests the hypothesis that age‐related changes in CFO in big brown bats ( Eptesicus fuscus ) differ from those of the standard mammalian model for skeletal aging, the C57BL/6 laboratory mouse. We used data from quantitative polarized light microscopy (qPLM) to compare CFO across the lifespan of long‐lived big brown bats and age matched C57BL/6 mice. Eptesicus and C57BL/6 mice displayed idiosyncratic patterns of CFO. Consistent age‐related changes were only apparent in the outer cortical bone of Eptesicus , where bone tissue is more longitudinally arranged and more anisotropic in older individuals. Both taxa displayed a ring of more transversely oriented bone tissue surrounding the medullary cavity. In Eptesicus , this tissue represents a greater proportion of the overall cross‐section, and is more clearly helically aligned (arranged at 45° to the bone long axis) than similar bone tissue in mice. Bat wing bones displayed a proximodistal gradient in CFO anisotropy and longitudinal orientation in both outer and inner cortical bone compartments. This study lays a methodological foundation for the quantitative evaluation of bone tissue architecture in volant and non‐volant mammals that may be expanded in the future.


Genetics of Evolved Load Resistance in the Skeletons of Unusually Large Mice from Gough Island

July 2023

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20 Reads

Genetics

A primary function of the skeleton is to resist the loads imparted by body weight. Genetic analyses have identified genomic regions that contribute to differences in skeletal load resistance between laboratory strains of mice, but these studies are usually restricted to one or two bones and leave open the question of how load resistance evolves in natural populations. To address these challenges, we examined the genetics of bone structure using the largest wild house mice on record, which live on Gough Island (GI). We measured structural traits connected to load resistance in the femur, tibia, scapula, humerus, radius, ulna, and mandible of GI mice, a smaller-bodied reference strain from the mainland, and 760 of their F2s. GI mice have bone geometries indicative of greater load resistance abilities but show no increase in bone mineral density compared to the mainland strain. Across traits and bones, we identified a total of 153 quantitative trait loci (QTL) that span all but one of the autosomes. The breadth of QTL detection ranges from a single bone to all seven bones. Additive effects of QTL are modest. QTL for bone structure show limited overlap with QTL for bone length and width and QTL for body weight mapped in the same cross, suggesting a distinct genetic architecture for load resistance. Our findings provide a rare genetic portrait of the evolution of load resistance in a natural population with extreme body size.


Trends in mandibular fractures in the USA: A 20-year retrospective analysis

June 2023

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20 Reads

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17 Citations

Dental Traumatology

Background/aim: The mandible is one of the most fractured bones in the maxillofacial region. This study analyzes trends in mandibular fracture patterns, demographics, and mechanisms since the early 2000s. Material and methods: Mandibular fractures were reviewed from the 2007, 2011, and 2017 National Trauma Data Bank including 13,142, 17,057, and 20,391 patients by year, respectively. This database contains hundreds of thousands of patients annually and represents the largest trauma registry in the United States. Variables included number of fractures, sex, age, injury mechanism, and fracture location. Mechanism of injury included assault, motor vehicle crash, fall, motorcycle, bicycle, pedestrian, and firearm. Anatomic locations based on ICD-9/10 codes included symphysis, ramus, condyle, condylar process, body, angle, and coronoid process. Frequencies were compared using Chi-square tests of homogeneity with effect sizes estimated using Cramer's V. Results: Mandibular fractures represent 2%-2.5% of all traumas reported in the database from 2001 to 2017. The proportion of patients sustaining a single reported mandibular fracture decreased from 82% in 2007 to 63% in 2017. Males consistently experienced 78%-80% of fractures. Eighteen to 54-year-olds experienced the largest percentages of fractures throughout the 21st century, while median age of fracture shifted from 28 to 32 between 2007 and 2017. The most common fracture mechanisms were assault (42% [2001-2005]-37% [2017]), motor vehicle crash (31%-22%) followed by falls (15%-20%). From 2001-2005 to 2017, a decrease was observed in assaults (-5%) and motor vehicle crash (-9%) and an increase in falls (+5%), particularly among elderly females. The mandibular body, condyle, angle, and symphysis represent approximately two-thirds of all fractures without a consistent temporal trend among them. Conclusions: The temporal trends observed can be linked to shifting age demographics nationally that may aid clinicians in diagnosis and inform public safety policies aimed at reducing these injuries, particularly among the growing elderly population.


Citations (62)


... PCSA is influenced most heavily by muscle mass and our muscle masses for the three jaw adductors are~56%-76% of those reported by Perry et al. (2011a; Table 3), with the greatest differences between our Varecia samples. A fair amount of within-species variation (including sexual size dimorphism) has been reported in strepsirrhines (e.g., Perry et al., 2011a;Taylor et al., 2024) and anthropoid primate chewing muscles (e.g., Terhune et al., 2015Terhune et al., , 2018. Thus, differences between our estimates could be the result of normal intraspecific variation. ...

Reference:

Tradeoffs between bite force and gape in Eulemur and Varecia
The impact of measurement technique and sampling on estimates of skeletal muscle fibre architecture

... Experiments based on limb-derived stem cells of Carollia and Eptesicus showed that, unlike those of mice, osteoprogenitor cells successfully differentiated into osteoblasts/osteocytes, produced a less mineralized matrix, and showed reduced transcripts of mineral-related genes.113 Compared to mice, adult bats display novel collagen fiber orientations within their bone matrix, which may offer some resilience to fragility with age.114 Beyond the matrix of bone, maintenance of the integrity of articular cartilage and skeletal muscle is critical for the survival of bats. ...

Comparing age‐ and bone‐related differences in collagen fiber orientation: A case study of bats and laboratory mice using quantitative polarized light microscopy

... With estimates ranging from around 2.8% in USA, 1.9% in China and 1.43% of all mandibular fractures in Iran. [19][20][21] Furthermore, isolated coronoid process fractures of iatrogenic origin are even rarer. 10 To our knowledge, there have only been three instances of previously reported cases in the literature. ...

Trends in mandibular fractures in the USA: A 20-year retrospective analysis
  • Citing Article
  • June 2023

Dental Traumatology

... For a preliminary assessment of age changes in growth plate microanatomy and wrist and ankle ossification, limb joints of one neonate and the 30-day-old were decalcified, paraffin embedded, and serially sectioned at 10 µm in a plane parallel to the long axis of long bones of each joint, and the wrist/hand and foot/ankle. Only specimens that had not been frozen were selected, for optimal preservation (i.e., lack of distortion that can accompany freezing - Wood et al., 2023). Sections were stained with Gomori trichrome, hematoxylin-eosin, or alcian blue-periodic acid-Schiff procedures. ...

Midline growth of the sphenoid bone in primates: A histological and microcomputed tomography study
  • Citing Article
  • November 2022

American Journal of Physical Anthropology

... A change in the body size, according to a so-called island rule, is the most studied of morphological peculiarities: during evolution, small vertebrates on the islands become larger than their mainland relatives, while large ones become smaller (Foster, 1964;Benítez-López et al., 2021). Characteristics of the locomotor apparatus change; for example, in island birds, the flight muscles become smaller and the legs become longer; the wings are reduced in some species (Wright et al., 2016); the size and shape of the mandible changes (Renaud and Auffray, 2010;Parmenter et al., 2022); changes in metabolism (McNab, 1994;Blanco et al., 2014) and the immune system (O' Connor et al., 2018) occur. The genetic (Funk et al., 2016) and demographic (Adler and Levins, 1994;Crespin et al., 2012) parameters of the population change. ...

A Complex Genetic Architecture Underlies Mandibular Evolution in Big Mice from Gough Island
  • Citing Article
  • February 2022

Genetics

... 2,6,7 Similarly, the movements of the hyoid bone during swallowing in humans and pigs occur in upward and forward directions coordinated by the hyoid muscles. [8][9][10] These movements of the hyoid bone also regulate the movements of pharyngeal structures such as the tongue base. ...

Anatomical and physiological variation of the hyoid musculature during swallowing in infant pigs
  • Citing Article
  • November 2021

Journal of Experimental Biology

... Kaidonis et al. [35] proposed a "scratch test" for clinicians with monitoring changes in striation depth or morphology over the course of days to show active wear. This mirrors work by Teaford and Oyen [36] and more recently Teaford and colleagues [37] aimed at documenting the turnover (appearance and disappearance) of individual microwear scratches and pits in vivo to assess rates of tooth wear at the micron scale. Further, Teaford and Tylenda [38] demonstrated that samples with faster microwear turnover (e.g. ...

Grit your teeth and chew your food: Implications of food material properties and abrasives for rates of dental microwear formation in laboratory Sapajus apella (Primates)
  • Citing Article
  • September 2021

Palaeogeography Palaeoclimatology Palaeoecology

... Sutures are fibrous joints in vertebrate craniofacial skeletons. Ontogenetically, they are important loci of craniofacial growth through their interactions with surrounding tissues and structures (Opperman, 2000;Maxson and Ishii, 2008;Liu et al., 2009;Zhao et al., 2015), their morphology and fusion patterns may be closely related to the function of the skull (i.e., Byron et al., 2004;Wang et al., 2006b,;Byron, 2009;Burrows et al., 2015). If disturbed, such as in the situation of premature closure, the normal growth of the skull will be disturbed resulting in abnormal skull shape as a consequence of adjusting growth direction (Cohen, 2000;Hanken and Gross, 2005;Rice, 2008). ...

Timing of Facial Suture Closure is Delayed in Gouging vs. Non‐Gouging Marmosets
  • Citing Article
  • April 2015

The FASEB Journal

... This last area has been considered by some authors as an authentic growth plate (Maat & Mastwijk, 1995), which is consistent with radiological evidence in humans (Madeline & Elster, 1995). Although there are no histological studies in humans that demonstrate that this area is a true synchondrosis, the existence of an active growth center in this region has been demonstrated histologically in other primates (Smith et al., 2021). ...

Cranial synchondroses of primates at birth

... Human systolic blood pressures, by way of contrast, are 120 mmHg [13,14]. The average lifespan of bowhead whales (Balaena mysticetus) is 211 years, while humans' average lifespan is 72 years, and small rodents, such as Chinese hamsters (Cricetulus griseus), live 2-3 years [15,16]. The variation in these traits and their correlations with IOP have rarely been investigated in non-humans. ...

Linking gene expression and phenotypic changes in the developmental and evolutionary origins of osteosclerosis in the ribs of bowhead whales ( Balaena mysticetus )

Journal of Experimental Zoology Part B Molecular and Developmental Evolution