The Early Pleistocene fossil site of Schernfeld, a karst fissure filled with an ossiferous breccia, is well known due to the abundant fossil remains, mainly of micromammals and carnivores. Since the discovery, the taxonomic status of the Schernfeld mustelids has caused controversy and, consequently, various authors have listed different species. Until recently, none of these species has been the subject of adequate studies. A detailed revision of the Schernfeld mustelids material was made through comparative morphology based on mustelids from other European Early and early Middle Pleistocene sites. It reveals the presence of five mustelids: Gulo gulo schlosseri, Martes vetus, Meles meles, Mustela palerminea, and Mustela praenivalis. Their remains are characterized by ancestral features, especially in M. vetus, M. palerminea, and M. praenivalis. Due to the morphology of mustelids and the taxonomical composition of the Schernfeld fauna, the biochronological age of the entire assemblage was re-evaluated and assessed for ca. 1.9–1.7 mya.
{"title":"Importance of the mustelids from the Early Pleistocene site Schernfeld (Bavaria, Germany) on the Eurasian context","authors":"Adrian Marciszak, Gertrud E. Rössner","doi":"10.1002/ar.25655","DOIUrl":"10.1002/ar.25655","url":null,"abstract":"<p>The Early Pleistocene fossil site of Schernfeld, a karst fissure filled with an ossiferous breccia, is well known due to the abundant fossil remains, mainly of micromammals and carnivores. Since the discovery, the taxonomic status of the Schernfeld mustelids has caused controversy and, consequently, various authors have listed different species. Until recently, none of these species has been the subject of adequate studies. A detailed revision of the Schernfeld mustelids material was made through comparative morphology based on mustelids from other European Early and early Middle Pleistocene sites. It reveals the presence of five mustelids: <i>Gulo gulo schlosseri</i>, <i>Martes vetus</i>, <i>Meles meles</i>, <i>Mustela palerminea</i>, and <i>Mustela praenivalis</i>. Their remains are characterized by ancestral features, especially in <i>M. vetus</i>, <i>M. palerminea</i>, and <i>M. praenivalis</i>. Due to the morphology of mustelids and the taxonomical composition of the Schernfeld fauna, the biochronological age of the entire assemblage was re-evaluated and assessed for ca. 1.9–1.7 mya.</p>","PeriodicalId":50965,"journal":{"name":"Anatomical Record-Advances in Integrative Anatomy and Evolutionary Biology","volume":"309 1","pages":"33-59"},"PeriodicalIF":2.1,"publicationDate":"2025-03-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143617779","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Jeffrey T. Laitman, Kimberly McKay, Heather F. Smith
<p>Animals, invertebrates, and vertebrates, are extraordinary creatures. So many components of their bodies have to work together to allow even basic functions to occur. Muscles have to move; cartilage, bone, and ligaments support; blood nourish; lymph clean; nerves communicate; and a host of histological tissue types provide substrate for it all. While the different parts of this intrinsic anatomical team must work together, there is one core system that must be present to keep the others working: the respiratory system. Indeed, aerobic respiration is the fundamental energy mechanism for higher life forms. Unless you are some fungi, most bacteria, tardigrades, Mediterranean Loricifera, an oddball African nematode, or some other anaerobic tidbit, oxygen is the holy grail. And respiration, through breathing or some other exchange modality, is the gold standard. Respiration is king.</p><p>One of the knights supporting this respiratory monarch is a focus of this Special Issue: Professor Kurt Albertine of the University of Utah School of Medicine. Kurt—our familiarity, as you will see, is too strong for formalities—is also the former Editor-in-Chief (EiC) of our journal. He has been, and always will be, a mentor, guide, stimulator, thought-provoker, and role model for us younger (ok, even a few older) folks. To say that we at <i>The Anatomical Record</i> adore him would be an understatement!</p><p>Kurt has had an illustrious career as a respiratory biologist, anatomical educator, mentor, and scholar (sort of, at least, as the former Editor of a great journal, i.e., ours.). First, as a bench scientist based since the Late Cretaceous (ok, since 1993) in the Department of Pediatrics at the University of Utah School of Medicine, Kurt and his minions (who he affectionately calls “his labbies” due to their caring of the research lambs used in his laboratory) have done insightful science exploring the basic biology of the developing mammalian lung sensu lato. In particular, his laboratory's investigations have focused upon acute and chronic pulmonary disease, with emphasis on neonatal lung disease. His work has targeted identification of molecular mechanisms that disrupt lung development in preterm neonates who require prolonged mechanical ventilation. Using the lung as focus, his lab has also explored how neonatal disturbance and disease affect molecular changes in other organs such as the brain, liver, and intestines. Recent work has even explored the bold hypothesis that preterm birth and prolonged mechanical ventilation can change epigenetic determinations of the regulation of gene expression. In essence, his studies take one back to the elements of the respiratory system as the driver of much of a mammal's core anatomy and physiology. Kurt's loving exploration of these underlying features in preterm lambs has been instrumental in helping the field of medicine to understand the etiology of postnatal lung disease and potential treatment in humans (see, e
{"title":"Breathing rarified air: The Anatomical Record celebrates Kurt Albertine with a Special Issue exploring new findings on respiratory biology","authors":"Jeffrey T. Laitman, Kimberly McKay, Heather F. Smith","doi":"10.1002/ar.25646","DOIUrl":"10.1002/ar.25646","url":null,"abstract":"<p>Animals, invertebrates, and vertebrates, are extraordinary creatures. So many components of their bodies have to work together to allow even basic functions to occur. Muscles have to move; cartilage, bone, and ligaments support; blood nourish; lymph clean; nerves communicate; and a host of histological tissue types provide substrate for it all. While the different parts of this intrinsic anatomical team must work together, there is one core system that must be present to keep the others working: the respiratory system. Indeed, aerobic respiration is the fundamental energy mechanism for higher life forms. Unless you are some fungi, most bacteria, tardigrades, Mediterranean Loricifera, an oddball African nematode, or some other anaerobic tidbit, oxygen is the holy grail. And respiration, through breathing or some other exchange modality, is the gold standard. Respiration is king.</p><p>One of the knights supporting this respiratory monarch is a focus of this Special Issue: Professor Kurt Albertine of the University of Utah School of Medicine. Kurt—our familiarity, as you will see, is too strong for formalities—is also the former Editor-in-Chief (EiC) of our journal. He has been, and always will be, a mentor, guide, stimulator, thought-provoker, and role model for us younger (ok, even a few older) folks. To say that we at <i>The Anatomical Record</i> adore him would be an understatement!</p><p>Kurt has had an illustrious career as a respiratory biologist, anatomical educator, mentor, and scholar (sort of, at least, as the former Editor of a great journal, i.e., ours.). First, as a bench scientist based since the Late Cretaceous (ok, since 1993) in the Department of Pediatrics at the University of Utah School of Medicine, Kurt and his minions (who he affectionately calls “his labbies” due to their caring of the research lambs used in his laboratory) have done insightful science exploring the basic biology of the developing mammalian lung sensu lato. In particular, his laboratory's investigations have focused upon acute and chronic pulmonary disease, with emphasis on neonatal lung disease. His work has targeted identification of molecular mechanisms that disrupt lung development in preterm neonates who require prolonged mechanical ventilation. Using the lung as focus, his lab has also explored how neonatal disturbance and disease affect molecular changes in other organs such as the brain, liver, and intestines. Recent work has even explored the bold hypothesis that preterm birth and prolonged mechanical ventilation can change epigenetic determinations of the regulation of gene expression. In essence, his studies take one back to the elements of the respiratory system as the driver of much of a mammal's core anatomy and physiology. Kurt's loving exploration of these underlying features in preterm lambs has been instrumental in helping the field of medicine to understand the etiology of postnatal lung disease and potential treatment in humans (see, e","PeriodicalId":50965,"journal":{"name":"Anatomical Record-Advances in Integrative Anatomy and Evolutionary Biology","volume":"308 4","pages":"1009-1017"},"PeriodicalIF":2.1,"publicationDate":"2025-02-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/ar.25646","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143525088","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Courtney A. Miller, Tanusha Emanuel, Rachel A. Menegaz
Early life behaviors have a profound role in shaping adult craniofacial morphology. During early life, all mammals undergo the dynamic transition from suckling to mastication, a period coinciding with rapid cranial biomineralization. Osteogenesis imperfecta (OI), a genetic disorder that impacts the production of type I collagen, disrupts biomineralization, leading to craniofacial growth differences affecting quality of life. This study investigates craniofacial development during infant oral motor developmental stages in OI mice compared to unaffected wild-type littermates (WT mice). We hypothesize OI mice will exhibit smaller overall size, and the adult OI phenotype will develop postnatally in response to masticatory loading. Point cloud and fixed landmarks were collected from micro-computed tomography scans, then geometric morphometric analyses and interlandmark distances (ILDs) compared craniofacial size and shape between OI and WT mice at birth (P0; n = 27 OI murine/20 WT) and postnatal Days 7 (P7; n = 21/21), 14 (P14; n = 16/20), 21 (P21; n = 20/26), and 28 (P28; n = 26/33). This study found no size and shape differences between genotypes at birth. Starting at P7, OI mice are significantly (p < 0.05) smaller and display pronounced shape changes (p < 0.001) characterized by a larger neurocranium and a shorter viscerocranium. At P21, significant differences emerge in cranial base orientation, neurocranial width, viscerocranial shortening, and zygomatic arch displacement. These findings underscore the importance of early life oral motor stages in developing the adult OI craniofacial phenotype and oral health, suggesting earlier craniofacial interventions may improve effective treatment of OI.
{"title":"Early life functional transitions impact craniofacial morphology in osteogenesis imperfecta","authors":"Courtney A. Miller, Tanusha Emanuel, Rachel A. Menegaz","doi":"10.1002/ar.25640","DOIUrl":"10.1002/ar.25640","url":null,"abstract":"<p>Early life behaviors have a profound role in shaping adult craniofacial morphology. During early life, all mammals undergo the dynamic transition from suckling to mastication, a period coinciding with rapid cranial biomineralization. Osteogenesis imperfecta (OI), a genetic disorder that impacts the production of type I collagen, disrupts biomineralization, leading to craniofacial growth differences affecting quality of life. This study investigates craniofacial development during infant oral motor developmental stages in OI mice compared to unaffected wild-type littermates (WT mice). We hypothesize OI mice will exhibit smaller overall size, and the adult OI phenotype will develop postnatally in response to masticatory loading. Point cloud and fixed landmarks were collected from micro-computed tomography scans, then geometric morphometric analyses and interlandmark distances (ILDs) compared craniofacial size and shape between OI and WT mice at birth (P0; <i>n</i> = 27 OI murine/20 WT) and postnatal Days 7 (P7; <i>n</i> = 21/21), 14 (P14; <i>n</i> = 16/20), 21 (P21; <i>n</i> = 20/26), and 28 (P28; <i>n</i> = 26/33). This study found no size and shape differences between genotypes at birth. Starting at P7, OI mice are significantly (<i>p</i> < 0.05) smaller and display pronounced shape changes (<i>p</i> < 0.001) characterized by a larger neurocranium and a shorter viscerocranium. At P21, significant differences emerge in cranial base orientation, neurocranial width, viscerocranial shortening, and zygomatic arch displacement. These findings underscore the importance of early life oral motor stages in developing the adult OI craniofacial phenotype and oral health, suggesting earlier craniofacial interventions may improve effective treatment of OI.</p>","PeriodicalId":50965,"journal":{"name":"Anatomical Record-Advances in Integrative Anatomy and Evolutionary Biology","volume":"308 12","pages":"3157-3174"},"PeriodicalIF":2.1,"publicationDate":"2025-02-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://anatomypubs.onlinelibrary.wiley.com/doi/epdf/10.1002/ar.25640","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143484584","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Sven Sachs, Daniel Madzia, Miguel Marx, Aubrey J. Roberts, Oliver Hampe, Benjamin P. Kear
Seeleyosaurus guilelmiimperatoris is an early-diverging plesiosauroid from the lower Toarcian (Lower Jurassic) of the Posidonienschiefer Formation (Posidonia Shale) of Holzmaden, southwestern Germany. It is known from almost complete skeletons of two osteologically mature individuals, the holotype and a referred specimen that was largely destroyed during World War II. Although well-preserved and substantially complete, the anatomy of Seeleyosaurus and its taxonomic and phylogenetic significance remain insufficiently understood. Here, we provide a complete osteological description of the taxon. Seeleyosaurus guilelmiimperatoris can be diagnosed based on a unique combination of characters, including one autapomorphy: the tall and basally constricted neural spines of the posterior cervical, pectoral, and dorsal vertebrae which have a sinusoidal shape in lateral view. Our study supports the validity of the plesiosauroid taxon Plesiopterys wildi, which was considered a junior synonym of Seeleyosaurus in a previous joint assessment of the taxa. Our phylogenetic evaluation places S. guilelmiimperatoris among Microcleididae, in congruence with previous studies. However, in contrast to earlier phylogenetic reconstructions, our analyses, which take into account numerous changes to the character matrix, reconstruct S. guilelmiimperatoris as falling within the Microcleidus clade. While we admit that Seeleyosaurus might potentially be considered a species of Microcleidus, we refrain from promoting this nomenclatural change pending an osteological and taxonomic reassessment of Microcleidus spp. as well as other, potentially closely related forms, such as Lusonectes sauvagei.
{"title":"The osteology, taxonomy, and phylogenetic placement of Seeleyosaurus guilelmiimperatoris (Plesiosauroidea, Microcleididae) from the Lower Jurassic Posidonia Shale of Germany","authors":"Sven Sachs, Daniel Madzia, Miguel Marx, Aubrey J. Roberts, Oliver Hampe, Benjamin P. Kear","doi":"10.1002/ar.25620","DOIUrl":"10.1002/ar.25620","url":null,"abstract":"<p><i>Seeleyosaurus guilelmiimperatoris</i> is an early-diverging plesiosauroid from the lower Toarcian (Lower Jurassic) of the Posidonienschiefer Formation (Posidonia Shale) of Holzmaden, southwestern Germany. It is known from almost complete skeletons of two osteologically mature individuals, the holotype and a referred specimen that was largely destroyed during World War II. Although well-preserved and substantially complete, the anatomy of <i>Seeleyosaurus</i> and its taxonomic and phylogenetic significance remain insufficiently understood. Here, we provide a complete osteological description of the taxon. <i>Seeleyosaurus guilelmiimperatoris</i> can be diagnosed based on a unique combination of characters, including one autapomorphy: the tall and basally constricted neural spines of the posterior cervical, pectoral, and dorsal vertebrae which have a sinusoidal shape in lateral view. Our study supports the validity of the plesiosauroid taxon <i>Plesiopterys wildi</i>, which was considered a junior synonym of <i>Seeleyosaurus</i> in a previous joint assessment of the taxa. Our phylogenetic evaluation places <i>S. guilelmiimperatoris</i> among Microcleididae, in congruence with previous studies. However, in contrast to earlier phylogenetic reconstructions, our analyses, which take into account numerous changes to the character matrix, reconstruct <i>S. guilelmiimperatoris</i> as falling within the <i>Microcleidus</i> clade. While we admit that <i>Seeleyosaurus</i> might potentially be considered a species of <i>Microcleidus</i>, we refrain from promoting this nomenclatural change pending an osteological and taxonomic reassessment of <i>Microcleidus</i> spp. as well as other, potentially closely related forms, such as <i>Lusonectes sauvagei</i>.</p>","PeriodicalId":50965,"journal":{"name":"Anatomical Record-Advances in Integrative Anatomy and Evolutionary Biology","volume":"308 9","pages":"2283-2346"},"PeriodicalIF":2.1,"publicationDate":"2025-02-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143469967","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Justin Keller, Annalisa Berta, Mark Juhn, Blaire Van Valkenburgh
Terrestrial vertebrates from at least 30 distinct lineages in both extinct and extant clades have returned to aquatic environments. With these transitions came numerous morphological adaptations to accommodate life in water. Relatively little attention has been paid to the cervical region when tracking this transition. In fully aquatic cetaceans, the cervical vertebrae are compressed, largely because a loss of neck mobility reduces drag. We ask whether this pattern of cervical evolution is present in the more recently evolved semiaquatic pinnipeds. Here, we compare neck morphology and function in three families of pinnipeds, the Otariidae, Phocidae, and Odobenidae as well as between pinnipeds and their terrestrial arctoid relatives (ursids and mustelids). Using cranial CT scans, we quantified the occipital surface area for neck muscle attachment as well as vertebral size and shape using linear measurements. Results show that pinnipeds have a relatively larger occipital surface area than ursids and terrestrial mustelids, suggesting that marine carnivorans have enlarged their neck muscles to assist with head stabilization during swimming. Within pinnipeds, we found quantitative differences in cervical morphology between otariids and phocids that coincide with their locomotor style. Phocids are hindlimb-dominated swimmers that propel themselves with pelvic oscillations. Their necks are relatively stiff and their cervical vertebrae are compressed anteroposteriorly with reduced muscular attachment areas. By contrast, otariids are forelimb-dominated swimmers that locomote in water and on land using their pectoral limbs, often recruiting their neck to initiate turns underwater as well as assisting in “walking” on land. Consequently, otariids have stronger, more flexible necks than phocids, which is reflected in more elongate cervical vertebral centra with larger muscle attachments. The walrus (Odobenidae) has a cervical vertebrae morphology intermediate to that of phocids and otariids, consistent with a phocid swimming mode combined with a more muscular neck that likely functions in intraspecific conflict and haul-out behavior.
{"title":"Morphology and function of pinniped necks: The long and short of it","authors":"Justin Keller, Annalisa Berta, Mark Juhn, Blaire Van Valkenburgh","doi":"10.1002/ar.25642","DOIUrl":"10.1002/ar.25642","url":null,"abstract":"<p>Terrestrial vertebrates from at least 30 distinct lineages in both extinct and extant clades have returned to aquatic environments. With these transitions came numerous morphological adaptations to accommodate life in water. Relatively little attention has been paid to the cervical region when tracking this transition. In fully aquatic cetaceans, the cervical vertebrae are compressed, largely because a loss of neck mobility reduces drag. We ask whether this pattern of cervical evolution is present in the more recently evolved semiaquatic pinnipeds. Here, we compare neck morphology and function in three families of pinnipeds, the Otariidae, Phocidae, and Odobenidae as well as between pinnipeds and their terrestrial arctoid relatives (ursids and mustelids). Using cranial CT scans, we quantified the occipital surface area for neck muscle attachment as well as vertebral size and shape using linear measurements. Results show that pinnipeds have a relatively larger occipital surface area than ursids and terrestrial mustelids, suggesting that marine carnivorans have enlarged their neck muscles to assist with head stabilization during swimming. Within pinnipeds, we found quantitative differences in cervical morphology between otariids and phocids that coincide with their locomotor style. Phocids are hindlimb-dominated swimmers that propel themselves with pelvic oscillations. Their necks are relatively stiff and their cervical vertebrae are compressed anteroposteriorly with reduced muscular attachment areas. By contrast, otariids are forelimb-dominated swimmers that locomote in water and on land using their pectoral limbs, often recruiting their neck to initiate turns underwater as well as assisting in “walking” on land. Consequently, otariids have stronger, more flexible necks than phocids, which is reflected in more elongate cervical vertebral centra with larger muscle attachments. The walrus (Odobenidae) has a cervical vertebrae morphology intermediate to that of phocids and otariids, consistent with a phocid swimming mode combined with a more muscular neck that likely functions in intraspecific conflict and haul-out behavior.</p>","PeriodicalId":50965,"journal":{"name":"Anatomical Record-Advances in Integrative Anatomy and Evolutionary Biology","volume":"308 12","pages":"3175-3185"},"PeriodicalIF":2.1,"publicationDate":"2025-02-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://anatomypubs.onlinelibrary.wiley.com/doi/epdf/10.1002/ar.25642","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143469964","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
The oval window (OW) is an opening connecting the inner and middle ear. Its area has been shown to consistently scale with body mass (BM) in primates, and has been used alongside semi-circular canal (SCC) size to differentiate Homo sapiens and fossil hominins, including Paranthropus robustus. However, while the morphology of other inner ear elements, such as cochlea and SCCs, has been extensively studied in primates, OW shape has received little attention. In this study, we assess OW morphological variability in extant primates, and compare P. robustus to extant hominids. The potential of OW size to predict BM is also assessed. For this, measurements were performed on 3D scans from extant primate species and of P. robustus from the sites of Kromdraai, Swartkrans, and Drimolen. Size was assessed using perimeter (OWP), area (OWA), and centroid size (OWCS). Shape was assessed using geometric morphometric methods. The OW has no sexual dimorphism; there is no size difference between juveniles and adults, but there is a slight shape difference between human juveniles and adults, with a seemingly opposite ontogenetic trajectory compared to other primates. P. robustus has an intermediary OW shape between apes and humans, with more ape-like specimens from Kromdraai and more human-like ones from Drimolen. Overall, OW morphology discriminates primate species well enough, especially H. sapiens. BM is well explained by OWA, but OWA is not reliable as a BM proxy due to high prediction errors. Nonetheless, the OWA of P. robustus suggests a BM close to that of a chimpanzee.
{"title":"The morphology of the oval window in Paranthropus robustus compared to humans and other modern primates.","authors":"Ruy Fernandez, José Braga","doi":"10.1002/ar.25644","DOIUrl":"https://doi.org/10.1002/ar.25644","url":null,"abstract":"<p><p>The oval window (OW) is an opening connecting the inner and middle ear. Its area has been shown to consistently scale with body mass (BM) in primates, and has been used alongside semi-circular canal (SCC) size to differentiate Homo sapiens and fossil hominins, including Paranthropus robustus. However, while the morphology of other inner ear elements, such as cochlea and SCCs, has been extensively studied in primates, OW shape has received little attention. In this study, we assess OW morphological variability in extant primates, and compare P. robustus to extant hominids. The potential of OW size to predict BM is also assessed. For this, measurements were performed on 3D scans from extant primate species and of P. robustus from the sites of Kromdraai, Swartkrans, and Drimolen. Size was assessed using perimeter (OWP), area (OWA), and centroid size (OWCS). Shape was assessed using geometric morphometric methods. The OW has no sexual dimorphism; there is no size difference between juveniles and adults, but there is a slight shape difference between human juveniles and adults, with a seemingly opposite ontogenetic trajectory compared to other primates. P. robustus has an intermediary OW shape between apes and humans, with more ape-like specimens from Kromdraai and more human-like ones from Drimolen. Overall, OW morphology discriminates primate species well enough, especially H. sapiens. BM is well explained by OWA, but OWA is not reliable as a BM proxy due to high prediction errors. Nonetheless, the OWA of P. robustus suggests a BM close to that of a chimpanzee.</p>","PeriodicalId":50965,"journal":{"name":"Anatomical Record-Advances in Integrative Anatomy and Evolutionary Biology","volume":" ","pages":""},"PeriodicalIF":1.8,"publicationDate":"2025-02-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143460498","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Chloé Lauer, Nicholas B. Holowka, Steven Worthington, Thomas S. Kraft, Ian J. Wallace
The feet of people in non-industrial societies often have higher, stiffer longitudinal arches (LAs) and larger intrinsic muscles than those of many people in post-industrial societies. The prevailing explanation for this phenomenon is that people in post-industrial societies commonly wear shoes that restrict foot mobility, while people in non-industrial societies are often habitually barefoot or minimally shod. However, people in post-industrial societies also tend to be less physically active than in non-industrial societies, and it is possible that this, too, is a major determinant of their foot form and function. Here, we test the hypothesis that among people in post-industrial societies, lower physical activity levels are associated with lower, less stiff LAs and smaller intrinsic muscles. In a cross-sectional analysis of 40 adults in the United States, none of whom were habitually barefoot or minimally shod, we measured daily physical activity using accelerometry, LA height and static stiffness using photography, LA dynamic stiffness using kinematic and kinetic data, and intrinsic muscle size using ultrasound. Using Bayesian models, we found very low probabilities of positive associations between physical activity (step count, time spent in moderate-to-vigorous activity) and LA height, LA static stiffness, and muscle size. For LA dynamic stiffness, we found small to moderate probabilities of positive associations with physical activity variables. These findings suggest that physical activity is unlikely a major determinant of variation in LA and intrinsic muscle form and function among post-industrial societies. It remains possible that physical activity affects LA and intrinsic muscle traits, but perhaps primarily among people who are habitually barefoot or minimally shod.
{"title":"Foot arch height, arch stiffness, and intrinsic muscle size are not strongly associated with daily physical activity levels in a cross-sectional study of adults in the United States","authors":"Chloé Lauer, Nicholas B. Holowka, Steven Worthington, Thomas S. Kraft, Ian J. Wallace","doi":"10.1002/ar.25639","DOIUrl":"10.1002/ar.25639","url":null,"abstract":"<p>The feet of people in non-industrial societies often have higher, stiffer longitudinal arches (LAs) and larger intrinsic muscles than those of many people in post-industrial societies. The prevailing explanation for this phenomenon is that people in post-industrial societies commonly wear shoes that restrict foot mobility, while people in non-industrial societies are often habitually barefoot or minimally shod. However, people in post-industrial societies also tend to be less physically active than in non-industrial societies, and it is possible that this, too, is a major determinant of their foot form and function. Here, we test the hypothesis that among people in post-industrial societies, lower physical activity levels are associated with lower, less stiff LAs and smaller intrinsic muscles. In a cross-sectional analysis of 40 adults in the United States, none of whom were habitually barefoot or minimally shod, we measured daily physical activity using accelerometry, LA height and static stiffness using photography, LA dynamic stiffness using kinematic and kinetic data, and intrinsic muscle size using ultrasound. Using Bayesian models, we found very low probabilities of positive associations between physical activity (step count, time spent in moderate-to-vigorous activity) and LA height, LA static stiffness, and muscle size. For LA dynamic stiffness, we found small to moderate probabilities of positive associations with physical activity variables. These findings suggest that physical activity is unlikely a major determinant of variation in LA and intrinsic muscle form and function among post-industrial societies. It remains possible that physical activity affects LA and intrinsic muscle traits, but perhaps primarily among people who are habitually barefoot or minimally shod.</p>","PeriodicalId":50965,"journal":{"name":"Anatomical Record-Advances in Integrative Anatomy and Evolutionary Biology","volume":"308 12","pages":"3259-3270"},"PeriodicalIF":2.1,"publicationDate":"2025-02-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143460496","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Colline Brassard, Lobna Wertani, Anthony Herrel, Hassen Jerbi
The impact of artificial selection on the masticatory apparatus of dogs has been poorly studied, and comparative data with dogs subjected to more natural constraints are lacking. This study explores the jaw musculature of Tunisian street dogs, which are largely free from the influence of breed-specific selection. The masticatory muscles (digastric, masseter, temporalis, and pterygoid) of 27 adult dogs were dissected and muscle mass and physiological cross-sectional area (PCSA) were quantified, providing a baseline for comparisons between dogs from more natural versus more controlled environments. Our findings reveal that the morphology of the jaw adductor muscles is remarkably conserved among dogs, despite significant variation in skull shape. Additionally, all masticatory muscles scale isometrically with body mass. Notably, females exhibit functional adaptations that optimize muscle strength, particularly in the temporalis muscle, despite showing smaller overall muscle volumes compared to males. This could be linked to differences in predation, competition for food, or factors related to sexual behavior. Preliminary evidence suggests that captivity may limit the development of muscle mass and PCSA in the temporalis muscle, likely due to changes in lifestyle and diet. Significant relationships were also observed between skull shape and muscle data, particularly in the mandible, indicating that skull variability reflects jaw adductor muscle anatomy to some degree. This study enhances our understanding of jaw muscle morphology and function in feral dog populations and offers insights into the adaptation of the masticatory apparatus in dogs.
{"title":"Variability of jaw muscles in Tunisian street dogs and adaptation to skull shape","authors":"Colline Brassard, Lobna Wertani, Anthony Herrel, Hassen Jerbi","doi":"10.1002/ar.25638","DOIUrl":"10.1002/ar.25638","url":null,"abstract":"<p>The impact of artificial selection on the masticatory apparatus of dogs has been poorly studied, and comparative data with dogs subjected to more natural constraints are lacking. This study explores the jaw musculature of Tunisian street dogs, which are largely free from the influence of breed-specific selection. The masticatory muscles (digastric, masseter, temporalis, and pterygoid) of 27 adult dogs were dissected and muscle mass and physiological cross-sectional area (PCSA) were quantified, providing a baseline for comparisons between dogs from more natural versus more controlled environments. Our findings reveal that the morphology of the jaw adductor muscles is remarkably conserved among dogs, despite significant variation in skull shape. Additionally, all masticatory muscles scale isometrically with body mass. Notably, females exhibit functional adaptations that optimize muscle strength, particularly in the temporalis muscle, despite showing smaller overall muscle volumes compared to males. This could be linked to differences in predation, competition for food, or factors related to sexual behavior. Preliminary evidence suggests that captivity may limit the development of muscle mass and PCSA in the temporalis muscle, likely due to changes in lifestyle and diet. Significant relationships were also observed between skull shape and muscle data, particularly in the mandible, indicating that skull variability reflects jaw adductor muscle anatomy to some degree. This study enhances our understanding of jaw muscle morphology and function in feral dog populations and offers insights into the adaptation of the masticatory apparatus in dogs.</p>","PeriodicalId":50965,"journal":{"name":"Anatomical Record-Advances in Integrative Anatomy and Evolutionary Biology","volume":"308 12","pages":"3122-3141"},"PeriodicalIF":2.1,"publicationDate":"2025-02-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://anatomypubs.onlinelibrary.wiley.com/doi/epdf/10.1002/ar.25638","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143450898","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Plutonium was discovered and first synthesized in the early 1940's. Several isotopes of plutonium are used in nuclear technologies, 238Pu for heat generation and 239Pu for energy production and weapons. Both isotopes emit alpha particles, which pose a significant radiation hazard when incorporated into the body. Alpha particles emitted during 239Pu decay deposit energy along a very short path in biological tissues (≈45 μm in soft tissues). Thus, defining the anatomical locations of these deposits is essential to identify the cells at risk of radiation damage and potential malignant transformation. Bone is a primary site for plutonium deposition and retention. Plutonium exposures are associated with increases in osteogenic cancers. Plutonium is preferentially deposited on endosteal and endocortical bone surfaces, particularly those surrounded by red versus yellow bone marrow. Red marrow is more vascularized with a sinusoid network, while yellow marrow is largely a closed capillary system. Cancellous bone in red marrow sites has greater bone turnover rates and relatively more plutonium-related bone cancers than in yellow marrow sites. The relationships of plutonium deposits in bone and potential alpha particle exposures to cells that include osteoclasts, reversal cells, canopy cells, osteoblasts, bone lining cells, and osteogenic progenitors of the basic multicellular unit during bone modeling and remodeling are reviewed. Differences in distributions of 239Pu versus naturally occurring tumors in humans and experimental animals are noted. This review emphasizes the importance of the anatomical locations of plutonium deposition and retention in the skeleton and the potential relative radiation risks from alpha particles to bone cells and their progenitors.
{"title":"Review of the anatomical basis for predicting plutonium alpha particle radiation induced osteogenic cancers","authors":"Scott C. Miller","doi":"10.1002/ar.25641","DOIUrl":"10.1002/ar.25641","url":null,"abstract":"<p>Plutonium was discovered and first synthesized in the early 1940's. Several isotopes of plutonium are used in nuclear technologies, <sup>238</sup>Pu for heat generation and <sup>239</sup>Pu for energy production and weapons. Both isotopes emit alpha particles, which pose a significant radiation hazard when incorporated into the body. Alpha particles emitted during <sup>239</sup>Pu decay deposit energy along a very short path in biological tissues (≈45 μm in soft tissues). Thus, defining the anatomical locations of these deposits is essential to identify the cells at risk of radiation damage and potential malignant transformation. Bone is a primary site for plutonium deposition and retention. Plutonium exposures are associated with increases in osteogenic cancers. Plutonium is preferentially deposited on endosteal and endocortical bone surfaces, particularly those surrounded by red versus yellow bone marrow. Red marrow is more vascularized with a sinusoid network, while yellow marrow is largely a closed capillary system. Cancellous bone in red marrow sites has greater bone turnover rates and relatively more plutonium-related bone cancers than in yellow marrow sites. The relationships of plutonium deposits in bone and potential alpha particle exposures to cells that include osteoclasts, reversal cells, canopy cells, osteoblasts, bone lining cells, and osteogenic progenitors of the basic multicellular unit during bone modeling and remodeling are reviewed. Differences in distributions of <sup>239</sup>Pu versus naturally occurring tumors in humans and experimental animals are noted. This review emphasizes the importance of the anatomical locations of plutonium deposition and retention in the skeleton and the potential relative radiation risks from alpha particles to bone cells and their progenitors.</p>","PeriodicalId":50965,"journal":{"name":"Anatomical Record-Advances in Integrative Anatomy and Evolutionary Biology","volume":"308 12","pages":"3197-3229"},"PeriodicalIF":2.1,"publicationDate":"2025-02-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12353174/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143442685","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Melissa D. Clarkson, Rhian R. Dunn, Joseph T. Hefner, Holly A. Long, Micayla C. Spiros
Due to its complex ossification during development, the superior region of the human occipital bone is a frequent site of supernumerary bones known as interparietal bones. Interparietal bones have been extensively studied across various disciplines, resulting in multiple classification schemes using icon-like graphics to represent categories of interparietal variants. However, disparities across these classification schemes reveal the need for a standardized system to facilitate comparisons and permit data pooling across studies. Based on an extensive literature review and the examination of physical specimens, a graphic library of 80 evidence-based graphics capturing interparietal variants was designed for community use. It provides five graphics of different morphologies of the lambdoid suture, 64 graphics of interparietal bones, six of ossicles at lambda, three of mendosal suture variants, and two of intrasutural ossicles. This approach allows additional graphics to be added in the future as needed. Graphics are compared to those from existing classification schemes and an exercise using the graphics to classify crania was performed. In the broadest sense, this research establishes a model for improved practices in representing and sharing morphological data.
{"title":"Human interparietal bones: Examination of existing classification schemes and development of a graphic library depicting variations","authors":"Melissa D. Clarkson, Rhian R. Dunn, Joseph T. Hefner, Holly A. Long, Micayla C. Spiros","doi":"10.1002/ar.25643","DOIUrl":"10.1002/ar.25643","url":null,"abstract":"<p>Due to its complex ossification during development, the superior region of the human occipital bone is a frequent site of supernumerary bones known as interparietal bones. Interparietal bones have been extensively studied across various disciplines, resulting in multiple classification schemes using icon-like graphics to represent categories of interparietal variants. However, disparities across these classification schemes reveal the need for a standardized system to facilitate comparisons and permit data pooling across studies. Based on an extensive literature review and the examination of physical specimens, a graphic library of 80 evidence-based graphics capturing interparietal variants was designed for community use. It provides five graphics of different morphologies of the lambdoid suture, 64 graphics of interparietal bones, six of ossicles at lambda, three of mendosal suture variants, and two of intrasutural ossicles. This approach allows additional graphics to be added in the future as needed. Graphics are compared to those from existing classification schemes and an exercise using the graphics to classify crania was performed. In the broadest sense, this research establishes a model for improved practices in representing and sharing morphological data.</p>","PeriodicalId":50965,"journal":{"name":"Anatomical Record-Advances in Integrative Anatomy and Evolutionary Biology","volume":"308 12","pages":"3186-3196"},"PeriodicalIF":2.1,"publicationDate":"2025-02-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12350755/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143426598","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}