Many planktonic rotifers carry their oviposited eggs until hatching. In some species, the eggs are attached to the mother via secretions from her style gland, which forms a thread that extends from her cloaca. In species of Pompholyx, the mother possesses the rare ability to change the tension on the secreted thread, which alters the proximity of the egg with respect to her body. In this study, we used behavioral observations, confocal microscopy, and transmission electron microscopy to study the functional morphology of the stalk gland, which secretes a similar thread to the style gland. Our observations reveal that six longitudinal muscles insert on a stalk-gland complex, which is a combination of a two-headed gland and an epithelial duct that connects to the posterior cloaca. The gland secretes a single, long, electron-dense thread that traverses the duct and attaches to the egg surface through the cloaca. Three retractor muscles insert on the stalk gland and function to pull the entire complex anteriorly, thereby increasing tension on the thread and moving the egg close to the mother's body. A set of three (two pairs and a single dorsal) protractor muscles antagonize these actions, and their contraction pulls the gland complex close to the cloaca, thereby releasing tension on the thread and allowing the egg to distance itself from the mother. The stalk gland complex does not appear to be homologous to the style glands of other rotifers, but we hypothesize that it functions as a form of maternal protection as is the case with style glands.
{"title":"Ultrastructure and Function of the Stalk Gland Complex of Pompholyx faciemlarva (Rotifera: Monogononta)","authors":"Thiago Quintão Araújo, Rick Hochberg","doi":"10.1002/jmor.70005","DOIUrl":"10.1002/jmor.70005","url":null,"abstract":"<p>Many planktonic rotifers carry their oviposited eggs until hatching. In some species, the eggs are attached to the mother via secretions from her style gland, which forms a thread that extends from her cloaca. In species of <i>Pompholyx</i>, the mother possesses the rare ability to change the tension on the secreted thread, which alters the proximity of the egg with respect to her body. In this study, we used behavioral observations, confocal microscopy, and transmission electron microscopy to study the functional morphology of the stalk gland, which secretes a similar thread to the style gland. Our observations reveal that six longitudinal muscles insert on a stalk-gland complex, which is a combination of a two-headed gland and an epithelial duct that connects to the posterior cloaca. The gland secretes a single, long, electron-dense thread that traverses the duct and attaches to the egg surface through the cloaca. Three retractor muscles insert on the stalk gland and function to pull the entire complex anteriorly, thereby increasing tension on the thread and moving the egg close to the mother's body. A set of three (two pairs and a single dorsal) protractor muscles antagonize these actions, and their contraction pulls the gland complex close to the cloaca, thereby releasing tension on the thread and allowing the egg to distance itself from the mother. The stalk gland complex does not appear to be homologous to the style glands of other rotifers, but we hypothesize that it functions as a form of maternal protection as is the case with style glands.</p>","PeriodicalId":16528,"journal":{"name":"Journal of Morphology","volume":"285 11","pages":""},"PeriodicalIF":1.5,"publicationDate":"2024-11-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/jmor.70005","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142622359","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}
Scott C. Pedersen, Chelsie C. G. Snipes, Richard T. Carter, Rolf Müller
The external ear in eutherian mammals is composed of the annular, auricular (pinna), and scutellar cartilages. The latter extends between the pinnae, across the top of the head, and lies at the intersection of numerous auricular muscles and is thought to be a sesamoid element. In bats, this scutulum consists of two distinct regions, (1) a thin squama that is in contact with the underlying temporalis fascia and (2) a lateral bossed portion that is lightly tethered to the medial surface of the pinna. The planar size, shape, and proportions of the squama vary by taxa, as does the relative size and thickness of the boss. The origins, insertions, and relative functions of the auricular muscles are complicated. Here, 30 muscles were tallied as to their primary attachment to the pinnae, scutula, or a pre-auricular musculo-aponeurotic plate that is derived from the epicranius. In contrast to Yangochiroptera, the origins and insertions of many auricular muscles have shifted from the scutulum to this aponeurotic plate, in both the Rhinolophidae and Hipposideridae. We propose that this functional shift is a derived character related primarily to the rapid translations and rotations of the pinna in high-duty-cycle rhinolophid and hipposiderid bats.
{"title":"The Scutulum and the Pre-Auricular Aponeurosis in Bats","authors":"Scott C. Pedersen, Chelsie C. G. Snipes, Richard T. Carter, Rolf Müller","doi":"10.1002/jmor.70006","DOIUrl":"10.1002/jmor.70006","url":null,"abstract":"<p>The external ear in eutherian mammals is composed of the annular, auricular (pinna), and scutellar cartilages. The latter extends between the pinnae, across the top of the head, and lies at the intersection of numerous auricular muscles and is thought to be a sesamoid element. In bats, this scutulum consists of two distinct regions, (1) a thin squama that is in contact with the underlying temporalis fascia and (2) a lateral bossed portion that is lightly tethered to the medial surface of the pinna. The planar size, shape, and proportions of the squama vary by taxa, as does the relative size and thickness of the boss. The origins, insertions, and relative functions of the auricular muscles are complicated. Here, 30 muscles were tallied as to their primary attachment to the pinnae, scutula, or a pre-auricular musculo-aponeurotic plate that is derived from the epicranius. In contrast to Yangochiroptera, the origins and insertions of many auricular muscles have shifted from the scutulum to this aponeurotic plate, in both the Rhinolophidae and Hipposideridae. We propose that this functional shift is a derived character related primarily to the rapid translations and rotations of the pinna in high-duty-cycle rhinolophid and hipposiderid bats.</p>","PeriodicalId":16528,"journal":{"name":"Journal of Morphology","volume":"285 11","pages":""},"PeriodicalIF":1.5,"publicationDate":"2024-11-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/jmor.70006","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142622357","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 craniocervical junction is the transition between the skull and the vertebral column that provides mobility while maintaining sufficient stability (i.e., protection of the brainstem and the spinal cord). The key elements involved are the occiput, the first cervical vertebra (CV1, atlas) and the second cervical vertebra (CV2, axis). The two vertebrae forming the atlas-axis complex are distinct in their morphology and differences in form have been linked to differences in ecological function in mammals. Here, we quantified the morphological diversity of the cranium, CV1 and CV2 in a sample of Carnivora using 3D geometric morphometrics to reveal phylogenetic and ecological patterns. Our results indicate that the observed variation in CV2 is related to the taxonomic diversity (i.e., strong phylogenetic signal), whereas variation in CV1 appears to be decoupled from species diversity in Carnivora and, thus, is likely to reflect a functional signal. The phylogenetically informed correlation analyses showed an association between the CV1 morphology and diet. Taxa that primarily feed on large prey tend to have larger transverse processes on CV1 which provides larger muscle attachment areas and may correlate with stronger muscles. The latter needs to be verified by future quantitative covariation analyses between bone and muscle data. Morphological peculiarities within Pinnipedia and Mustelidae could be explained by differences in terrestrial locomotion between Phocidae and Otariidae and the exceptional defensive behavior (i.e., handstanding) in Mephitidae. Despite differences in the degree of morphological diversity, covariation between cranium, CV1 and CV2 morphology is consistently high (≥ 0.82) highlighting that overall, the craniocervical junction is an integrated structure, but there are traits that are not constrained.
{"title":"Covariation in the Craniocervical Junction of Carnivora","authors":"Christine Böhmer, Mara Destina Ocak","doi":"10.1002/jmor.70009","DOIUrl":"10.1002/jmor.70009","url":null,"abstract":"<p>The craniocervical junction is the transition between the skull and the vertebral column that provides mobility while maintaining sufficient stability (i.e., protection of the brainstem and the spinal cord). The key elements involved are the occiput, the first cervical vertebra (CV1, atlas) and the second cervical vertebra (CV2, axis). The two vertebrae forming the atlas-axis complex are distinct in their morphology and differences in form have been linked to differences in ecological function in mammals. Here, we quantified the morphological diversity of the cranium, CV1 and CV2 in a sample of Carnivora using 3D geometric morphometrics to reveal phylogenetic and ecological patterns. Our results indicate that the observed variation in CV2 is related to the taxonomic diversity (i.e., strong phylogenetic signal), whereas variation in CV1 appears to be decoupled from species diversity in Carnivora and, thus, is likely to reflect a functional signal. The phylogenetically informed correlation analyses showed an association between the CV1 morphology and diet. Taxa that primarily feed on large prey tend to have larger transverse processes on CV1 which provides larger muscle attachment areas and may correlate with stronger muscles. The latter needs to be verified by future quantitative covariation analyses between bone and muscle data. Morphological peculiarities within Pinnipedia and Mustelidae could be explained by differences in terrestrial locomotion between Phocidae and Otariidae and the exceptional defensive behavior (i.e., handstanding) in Mephitidae. Despite differences in the degree of morphological diversity, covariation between cranium, CV1 and CV2 morphology is consistently high (≥ 0.82) highlighting that overall, the craniocervical junction is an integrated structure, but there are traits that are not constrained.</p>","PeriodicalId":16528,"journal":{"name":"Journal of Morphology","volume":"285 11","pages":""},"PeriodicalIF":1.5,"publicationDate":"2024-11-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/jmor.70009","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142622355","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}