Pub Date : 2025-01-12DOI: 10.1016/j.asd.2024.101408
Nicole Schröter, Urska Repnik, Dirk Brandis
The objective of this study is to gain a better understanding of the not well understood egg-transportation mechanisms through the female reproductive systems of crabs. For this, Carcinus maenas was chosen as a model to study the cuticular epithelium underlying the cuticle of the vagina and the ventral seminal receptacle. This cuticular epithelium is investigated by performing histochemical and ultrastructural analyses of the epithelial cells. The results show that this epithelium consists of specialized epithelial cells that show characteristic features of muscle-attachment cells or tendon cells, such as an abundance of microtubules in their cytoplasm and hemi-adherens junctions. These results improve our understanding of the mechanisms involved in the reproduction in brachyuran crabs and will have to be taken into consideration in the future, when trying to understand the functional morphology of the female reproductive system of crabs.
{"title":"Insights into morphology of the 'columnar epithelium' within the female reproductive system of brachyuran crabs.","authors":"Nicole Schröter, Urska Repnik, Dirk Brandis","doi":"10.1016/j.asd.2024.101408","DOIUrl":"https://doi.org/10.1016/j.asd.2024.101408","url":null,"abstract":"<p><p>The objective of this study is to gain a better understanding of the not well understood egg-transportation mechanisms through the female reproductive systems of crabs. For this, Carcinus maenas was chosen as a model to study the cuticular epithelium underlying the cuticle of the vagina and the ventral seminal receptacle. This cuticular epithelium is investigated by performing histochemical and ultrastructural analyses of the epithelial cells. The results show that this epithelium consists of specialized epithelial cells that show characteristic features of muscle-attachment cells or tendon cells, such as an abundance of microtubules in their cytoplasm and hemi-adherens junctions. These results improve our understanding of the mechanisms involved in the reproduction in brachyuran crabs and will have to be taken into consideration in the future, when trying to understand the functional morphology of the female reproductive system of crabs.</p>","PeriodicalId":55461,"journal":{"name":"Arthropod Structure & Development","volume":"84 ","pages":"101408"},"PeriodicalIF":1.7,"publicationDate":"2025-01-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142980444","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-12-12DOI: 10.1016/j.asd.2024.101405
Tobias Pfingstl, Michaela Kerschbaumer
Claw characteristics of oribatid mites are strongly correlated with environmental factors and these characters remain constant throughout development when immatures and adults share the same ecology and lifestyle. In the present study, claw traits of oribatid mite species with constant ecology were compared with those of species showing a clear ecological shift between juvenile and adult stage. The arboreal Sellnickia caudata and the saxicolous Niphocepheus nivalis dwell in the same microhabitat during their life-cycle, whereas immatures of the terrestrial Carabodes areolatus and Mycobates carli, as well as of the aquatic Hydrozetes lemnae, are, in contrast to their adults, endophagous, meaning they feed and burrow within lichen and plant tissue. We performed a geometric morphometric investigation of their claws and could reveal significant differences in the claw shapes of immatures and adults of all species, except for N. nivalis. Claws of the endophagous juveniles of C. areolatus, M. carli and H. lemnae are generally sharper and higher than those of their adult counterparts. The burrowing lifestyle of the immatures apparently necessitates such specific claw morphologies. Despite having a constant ecology, the arboreal S. caudata also shows distinct differences between immature and adult claw traits, with juveniles possessing stronger curved and sharper claws. But immature stages also possess an additional tarsal adhesive pad which lacks in the adult stage. The presence or absence of this additional adhesive pad apparently requires changes in claw morphology to allow firm attachment on diverse plant surfaces. The present results demonstrate that claw characteristic can change during the development depending on the given ecological factors faced by each developmental stage and depending on the presence of additional attachment devices.
{"title":"It's 'claw'-some: Ontogenetic claw shape changes in mites (Acari, Oribatida) as a consequence of ecological shifts.","authors":"Tobias Pfingstl, Michaela Kerschbaumer","doi":"10.1016/j.asd.2024.101405","DOIUrl":"https://doi.org/10.1016/j.asd.2024.101405","url":null,"abstract":"<p><p>Claw characteristics of oribatid mites are strongly correlated with environmental factors and these characters remain constant throughout development when immatures and adults share the same ecology and lifestyle. In the present study, claw traits of oribatid mite species with constant ecology were compared with those of species showing a clear ecological shift between juvenile and adult stage. The arboreal Sellnickia caudata and the saxicolous Niphocepheus nivalis dwell in the same microhabitat during their life-cycle, whereas immatures of the terrestrial Carabodes areolatus and Mycobates carli, as well as of the aquatic Hydrozetes lemnae, are, in contrast to their adults, endophagous, meaning they feed and burrow within lichen and plant tissue. We performed a geometric morphometric investigation of their claws and could reveal significant differences in the claw shapes of immatures and adults of all species, except for N. nivalis. Claws of the endophagous juveniles of C. areolatus, M. carli and H. lemnae are generally sharper and higher than those of their adult counterparts. The burrowing lifestyle of the immatures apparently necessitates such specific claw morphologies. Despite having a constant ecology, the arboreal S. caudata also shows distinct differences between immature and adult claw traits, with juveniles possessing stronger curved and sharper claws. But immature stages also possess an additional tarsal adhesive pad which lacks in the adult stage. The presence or absence of this additional adhesive pad apparently requires changes in claw morphology to allow firm attachment on diverse plant surfaces. The present results demonstrate that claw characteristic can change during the development depending on the given ecological factors faced by each developmental stage and depending on the presence of additional attachment devices.</p>","PeriodicalId":55461,"journal":{"name":"Arthropod Structure & Development","volume":"84 ","pages":"101405"},"PeriodicalIF":1.7,"publicationDate":"2024-12-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142822967","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-11-01Epub Date: 2024-12-04DOI: 10.1016/j.asd.2024.101403
Nina Alexeeva, Ekaterina Bogomolova, Yuta Tamberg
All major arthropod taxa possess excretory glands - a type of filtration nephridium considered ancestral for this group. Pycnogonids form a basal branch of the arthropod phylogenetic tree and are ancient aquatic chelicerates, but they were believed to lack specialised excretory organs, except for Nymphopsis spinosissimum (Ammotheidae). Whether this condition is unique or common remained unknown due to lack of anatomical data for many species. Here we examined four nymphonids: Nymphon brevirostre, Nymphon grossipes, Nymphon serratum and Pentanymphon antarcticum using scanning and transmission electron microscopy, as well as light microscopy. In adults of all four species, we found excretory organs and describe ultrastructural details of all their parts: sacculus, reabsorption channel, excretory channel and the pore. In addition to the definitive (adult) excretory organs, we also detected some larval and juvenile transitory ones and were able to trace the origin of the sacculus podocytes from the non-epithelial mesoderm of the horizontal septum. All excretory organs are located in the appendages of the first three postocular segments of the cephalosoma (although not necessarily in all of them at once) because these areas can maintain the high hemolymph pressure necessary for ultrafiltration. The ultrastructure and development of the sacculus point toward the secondary nature of this cavity, although the coelomic status of the sacculi in sea spiders and other arthropods is still unclear.
{"title":"Excretory glands of sea spiders (Pycnogonida, Nymphonidae).","authors":"Nina Alexeeva, Ekaterina Bogomolova, Yuta Tamberg","doi":"10.1016/j.asd.2024.101403","DOIUrl":"10.1016/j.asd.2024.101403","url":null,"abstract":"<p><p>All major arthropod taxa possess excretory glands - a type of filtration nephridium considered ancestral for this group. Pycnogonids form a basal branch of the arthropod phylogenetic tree and are ancient aquatic chelicerates, but they were believed to lack specialised excretory organs, except for Nymphopsis spinosissimum (Ammotheidae). Whether this condition is unique or common remained unknown due to lack of anatomical data for many species. Here we examined four nymphonids: Nymphon brevirostre, Nymphon grossipes, Nymphon serratum and Pentanymphon antarcticum using scanning and transmission electron microscopy, as well as light microscopy. In adults of all four species, we found excretory organs and describe ultrastructural details of all their parts: sacculus, reabsorption channel, excretory channel and the pore. In addition to the definitive (adult) excretory organs, we also detected some larval and juvenile transitory ones and were able to trace the origin of the sacculus podocytes from the non-epithelial mesoderm of the horizontal septum. All excretory organs are located in the appendages of the first three postocular segments of the cephalosoma (although not necessarily in all of them at once) because these areas can maintain the high hemolymph pressure necessary for ultrafiltration. The ultrastructure and development of the sacculus point toward the secondary nature of this cavity, although the coelomic status of the sacculi in sea spiders and other arthropods is still unclear.</p>","PeriodicalId":55461,"journal":{"name":"Arthropod Structure & Development","volume":" ","pages":"101403"},"PeriodicalIF":1.7,"publicationDate":"2024-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142781895","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-11-01Epub Date: 2024-12-04DOI: 10.1016/j.asd.2024.101404
Maria Petrova, Ekaterina Bogomolova
Sea spiders (Pycnogonida) are marine chelicerates. As a sister clade to Euchelicerata, Pycnogonida are an interesting group for comparative anatomy, however data on pycnogonid anatomy and biology remain scarce. This research provides a detailed account of the complete male reproductive system, gametogenesis, and sperm structure of a sea spider at the ultrastructural level. The male reproductive system of P. femoratum includes the testis, femoral, and ovigeral glands. The testis is typical of Pycnogonida: U-shaped with pedal outgrowths, opening with gonopores on legs 2-4. The testis lays within the horizontal septum, separated from it by ECM. The reproductive sinus is reduced. The ventral wall of the testis is germinative, spermatogenesis proceeds in cysts, all stages are evenly distributed throughout the whole testis. Sperm of P. femoratum is a typical sperm of animals with fertilization in mucus but without an acrosome. It lacks apomorphic euchelicerate features such as an acrosomal filament and implantation fossa. Femoral and ovigeral glands are sex-specific and likely related to reproduction. Ovigeral glands possibly secrete a fungicide substance, while the function of femoral glands remains obscure.
{"title":"The male reproductive system of the sea spider Phoxichilidium femoratum (Rathke, 1799).","authors":"Maria Petrova, Ekaterina Bogomolova","doi":"10.1016/j.asd.2024.101404","DOIUrl":"10.1016/j.asd.2024.101404","url":null,"abstract":"<p><p>Sea spiders (Pycnogonida) are marine chelicerates. As a sister clade to Euchelicerata, Pycnogonida are an interesting group for comparative anatomy, however data on pycnogonid anatomy and biology remain scarce. This research provides a detailed account of the complete male reproductive system, gametogenesis, and sperm structure of a sea spider at the ultrastructural level. The male reproductive system of P. femoratum includes the testis, femoral, and ovigeral glands. The testis is typical of Pycnogonida: U-shaped with pedal outgrowths, opening with gonopores on legs 2-4. The testis lays within the horizontal septum, separated from it by ECM. The reproductive sinus is reduced. The ventral wall of the testis is germinative, spermatogenesis proceeds in cysts, all stages are evenly distributed throughout the whole testis. Sperm of P. femoratum is a typical sperm of animals with fertilization in mucus but without an acrosome. It lacks apomorphic euchelicerate features such as an acrosomal filament and implantation fossa. Femoral and ovigeral glands are sex-specific and likely related to reproduction. Ovigeral glands possibly secrete a fungicide substance, while the function of femoral glands remains obscure.</p>","PeriodicalId":55461,"journal":{"name":"Arthropod Structure & Development","volume":" ","pages":"101404"},"PeriodicalIF":1.7,"publicationDate":"2024-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142787962","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-10-19DOI: 10.1016/j.asd.2024.101392
Emma J. Long , Gregory D. Edgecombe , Paul Kenrick , Xiaoya Ma
The cuticle is a key evolutionary innovation that played a crucial role in arthropod terrestrialization. Extensive research has elucidated the chemical and structural composition of the cuticle in extant arthropods, while fossil studies have further informed our understanding of cuticle evolution. This study examines the three-dimensionally preserved cuticular structure of the Early Devonian trigonotarbid arachnid genus Palaeocharinus, from the Rhynie chert of Scotland (∼408 Ma). Trigonotarbids, an extinct group of tetrapulmonate arachnids, are among the earliest known unequivocally terrestrial arthropods, and thus may shed light on the evolution of terrestriality. Using high-resolution Confocal Laser Scanning Microscopy (CLSM), we reveal detailed morphological features at the nanometre level. The external cuticle surface of Palaeocharinus is characterized by polygonal scales, sensilla, and small pores identified as the openings of dermal glands and wax canals. Internally, the cuticle exhibits polygonal clusters of pore canals, through which wax was transported from the epidermis to the cuticular surface. The pore canals twist along their vertical axes, reflecting the "twisted plywood" or Bouligand arrangement of chitin-protein microfibril planes characteristic of modern arthropod cuticles. Overall, the cuticle of Palaeocharinus is characteristically thick relative to those of other extinct and extant chelicerates, such thickening being a possible adaptation to terrestrial life.
{"title":"Cuticle ultrastructure of the Early Devonian trigonotarbid arachnid Palaeocharinus","authors":"Emma J. Long , Gregory D. Edgecombe , Paul Kenrick , Xiaoya Ma","doi":"10.1016/j.asd.2024.101392","DOIUrl":"10.1016/j.asd.2024.101392","url":null,"abstract":"<div><div>The cuticle is a key evolutionary innovation that played a crucial role in arthropod terrestrialization. Extensive research has elucidated the chemical and structural composition of the cuticle in extant arthropods, while fossil studies have further informed our understanding of cuticle evolution. This study examines the three-dimensionally preserved cuticular structure of the Early Devonian trigonotarbid arachnid genus <em>Palaeocharinus</em>, from the Rhynie chert of Scotland (∼408 Ma). Trigonotarbids, an extinct group of tetrapulmonate arachnids, are among the earliest known unequivocally terrestrial arthropods, and thus may shed light on the evolution of terrestriality. Using high-resolution Confocal Laser Scanning Microscopy (CLSM), we reveal detailed morphological features at the nanometre level. The external cuticle surface of <em>Palaeocharinus</em> is characterized by polygonal scales, sensilla, and small pores identified as the openings of dermal glands and wax canals. Internally, the cuticle exhibits polygonal clusters of pore canals, through which wax was transported from the epidermis to the cuticular surface. The pore canals twist along their vertical axes, reflecting the \"twisted plywood\" or Bouligand arrangement of chitin-protein microfibril planes characteristic of modern arthropod cuticles. Overall, the cuticle of <em>Palaeocharinus</em> is characteristically thick relative to those of other extinct and extant chelicerates, such thickening being a possible adaptation to terrestrial life.</div></div>","PeriodicalId":55461,"journal":{"name":"Arthropod Structure & Development","volume":"83 ","pages":"Article 101392"},"PeriodicalIF":1.7,"publicationDate":"2024-10-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142481639","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-10-18DOI: 10.1016/j.asd.2024.101393
Jakob Krieger , Torsten Fregin , Steffen Harzsch
Members of the Euphausiacea (“krill”) generate bioluminescence using light organs, the so-called photophores, including one pair associated with the eyestalks, two pairs on the thoracic segments, and four unpaired photophores on the pleon. The photophores generate light via a luciferin–luciferase type of biochemical reaction in light-emitting cells comprised in a photophore compartment called “lantern”. The behavioral significance of bioluminescence in krill is discussed controversially, and possible functions include a defensive function, camouflage by counter-shading, and intra-specific communication. Light production of all krill photophores is controlled by hormonal and neuronal pathways but our knowledge about the nature of these pathways is still rudimentary. Here, we provide a detailed description of the eyestalk photophore's histology in Northern krill Meganyctiphanes norvegica, and used immunohistochemistry combined with confocal laser-scan microscopy to explore this organ's serotonergic innervation. Furthermore, we provide evidence that the photophore is innervated by a distinct photophore nerve that originates from a specialized cluster of ca. 30 highly modified ommatidia at the dorsal rim of the compound eye that are optically isolated from the other ommatidia. Our findings suggest the compound eye – photophore link as a major anatomical axis to adjust the photophore activity.
{"title":"The eyestalk photophore of Northern krill Meganyctiphanes norvegica (M. Sars) (Euphausiacea) re-investigated: Innervation by specialized ommatidia of the compound eye","authors":"Jakob Krieger , Torsten Fregin , Steffen Harzsch","doi":"10.1016/j.asd.2024.101393","DOIUrl":"10.1016/j.asd.2024.101393","url":null,"abstract":"<div><div>Members of the Euphausiacea (“krill”) generate bioluminescence using light organs, the so-called photophores, including one pair associated with the eyestalks, two pairs on the thoracic segments, and four unpaired photophores on the pleon. The photophores generate light <em>via</em> a luciferin–luciferase type of biochemical reaction in light-emitting cells comprised in a photophore compartment called “lantern”. The behavioral significance of bioluminescence in krill is discussed controversially, and possible functions include a defensive function, camouflage by counter-shading, and intra-specific communication. Light production of all krill photophores is controlled by hormonal and neuronal pathways but our knowledge about the nature of these pathways is still rudimentary. Here, we provide a detailed description of the eyestalk photophore's histology in Northern krill <em>Meganyctiphanes norvegica</em>, and used immunohistochemistry combined with confocal laser-scan microscopy to explore this organ's serotonergic innervation. Furthermore, we provide evidence that the photophore is innervated by a distinct photophore nerve that originates from a specialized cluster of ca. 30 highly modified ommatidia at the dorsal rim of the compound eye that are optically isolated from the other ommatidia. Our findings suggest the compound eye – photophore link as a major anatomical axis to adjust the photophore activity.</div></div>","PeriodicalId":55461,"journal":{"name":"Arthropod Structure & Development","volume":"83 ","pages":"Article 101393"},"PeriodicalIF":1.7,"publicationDate":"2024-10-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142481642","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-10-18DOI: 10.1016/j.asd.2024.101394
Pyotr N. Petrov, Natalia I. Reshetnikova, Sergey E. Farisenkov, Alexey A. Polilov
The ability to fold the wings is an important phenomenon in insect evolution and a feature that attracts the attention of engineers who develop biomimetic technologies. Beetles of the family Ptiliidae (featherwing beetles) are unique among microinsects in their ability to fold their bristled wings under the elytra and unfold them before flight. The folding and unfolding of bristled wings and of the structures involved in these processes varies among ptiliids, but only one species, Acrotrichis sericans, has been analyzed in detail. In this study, we analyze in detail the wing folding pattern and the mechanism of the folding and unfolding of the wings in species of different lineages of Ptiliidae, using scanning electron, сonfocal laser scanning, and optical microscopy, and compare the wing-folding patterns of Ptiliidae with those of the sister group, Hydraenidae, to reconstruct the evolution of the involved structures. We confirm that the two subfamilies of Ptiliidae have two distinct patterns of wing folding: Nossidiinae has retained the ancestral (‘agyrtid’) asymmetrical pattern with overlapping wings and with folds at different angles to the wing axis, while Ptiliinae, which includes the smallest of all known beetles, has evolved a symmetrical pattern with non-overlapping wings and folds perpendicular to the wing axis, with one additional oblique fold in the genus Ptenidium. Ptiliids have a longer alacrista, which helps to lock the elytra at rest, and a more complex set of structures involved in wing folding on abdominal tergites. These genus-specific structures, which include setae and wing-folding patches on some of the tergites and the palisade fringe of setae on the posterior margin of tergite 7, help the insect to tuck the wing under the elytron and fold it after flight. The symmetrical wing-folding pattern is simpler than the wing folding patterns of most larger beetles. The obtained data on the mechanisms and patterns of the folding and unfolding of the wings in Ptiliidae elucidate the evolution of wing folding as an adaptation protecting the wings at rest. Structures involved in wing folding can be used as distinguishing characters in taxonomy. The wing-folding mechanisms of Ptiliidae may eventually be used for developing miniature biomimetic robots.
{"title":"Evolution of and structures involved in wing folding in featherwing beetles (Coleoptera: Ptiliidae)","authors":"Pyotr N. Petrov, Natalia I. Reshetnikova, Sergey E. Farisenkov, Alexey A. Polilov","doi":"10.1016/j.asd.2024.101394","DOIUrl":"10.1016/j.asd.2024.101394","url":null,"abstract":"<div><div>The ability to fold the wings is an important phenomenon in insect evolution and a feature that attracts the attention of engineers who develop biomimetic technologies. Beetles of the family Ptiliidae (featherwing beetles) are unique among microinsects in their ability to fold their bristled wings under the elytra and unfold them before flight. The folding and unfolding of bristled wings and of the structures involved in these processes varies among ptiliids, but only one species, <em>Acrotrichis sericans,</em> has been analyzed in detail<em>.</em> In this study, we analyze in detail the wing folding pattern and the mechanism of the folding and unfolding of the wings in species of different lineages of Ptiliidae, using scanning electron, сonfocal laser scanning, and optical microscopy, and compare the wing-folding patterns of Ptiliidae with those of the sister group, Hydraenidae, to reconstruct the evolution of the involved structures. We confirm that the two subfamilies of Ptiliidae have two distinct patterns of wing folding: Nossidiinae has retained the ancestral (‘agyrtid’) asymmetrical pattern with overlapping wings and with folds at different angles to the wing axis, while Ptiliinae, which includes the smallest of all known beetles, has evolved a symmetrical pattern with non-overlapping wings and folds perpendicular to the wing axis, with one additional oblique fold in the genus <em>Ptenidium</em>. Ptiliids have a longer alacrista, which helps to lock the elytra at rest, and a more complex set of structures involved in wing folding on abdominal tergites. These genus-specific structures, which include setae and wing-folding patches on some of the tergites and the palisade fringe of setae on the posterior margin of tergite 7, help the insect to tuck the wing under the elytron and fold it after flight. The symmetrical wing-folding pattern is simpler than the wing folding patterns of most larger beetles. The obtained data on the mechanisms and patterns of the folding and unfolding of the wings in Ptiliidae elucidate the evolution of wing folding as an adaptation protecting the wings at rest. Structures involved in wing folding can be used as distinguishing characters in taxonomy. The wing-folding mechanisms of Ptiliidae may eventually be used for developing miniature biomimetic robots.</div></div>","PeriodicalId":55461,"journal":{"name":"Arthropod Structure & Development","volume":"83 ","pages":"Article 101394"},"PeriodicalIF":1.7,"publicationDate":"2024-10-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142481640","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-10-18DOI: 10.1016/j.asd.2024.101395
Nina Alexeeva, Daria Martynova
The family Callipallenidae Hilton, 1942 belongs to the superfamily Nymphonoidea Pocock, 1904 together with other family, Nymphonidae. The lecithotrophic postlarvae hatch from the eggs of the callipallenid sea spiders, but the data on this life stage are very scarce and fragmentary. This gives a very limited understanding of larval anatomy, morphology, and diversity. The larvae of Austropallene bucera Pushkin, 1993, Austropallene calmani Gordon, 1944, and Austropallene cristata Bouvier, 1911 have been studied and described for the first time by the methods of light (LM) and scanning electron microscopy (SEM). The main morphometry parameters have been determined in larvae and adult egg-bearing males. The general plan of the postlarvae is presented together with its specific features. The postlarvae of the studied Austropallene species combine the features of lecithotrophic and free-living pycnogonid larvae. The diversity of larvae in the Nymphonoidea superfamily has been analysed considering original and published data, and a morphological series has been developed. The complex of lecithotrophic larvae, like postlarvae of Callipallenidae, should be considered as primary for the entire superfamily. It is also suggested that sea spiders with lecithotrophic larvae tend to follow the K-strategy, but they care for their offspring to varying degrees.
{"title":"Morphology of lecithotrophic postlarvae of genus Austropallene (Arthropoda: Chelicerata) with some notes on reproductive strategy","authors":"Nina Alexeeva, Daria Martynova","doi":"10.1016/j.asd.2024.101395","DOIUrl":"10.1016/j.asd.2024.101395","url":null,"abstract":"<div><div>The family Callipallenidae Hilton, 1942 belongs to the superfamily Nymphonoidea Pocock, 1904 together with other family, Nymphonidae. The lecithotrophic postlarvae hatch from the eggs of the callipallenid sea spiders, but the data on this life stage are very scarce and fragmentary. This gives a very limited understanding of larval anatomy, morphology, and diversity. The larvae of <em>Austropallene bucera</em> Pushkin, 1993, <em>Austropallene calmani</em> Gordon, 1944, and <em>Austropallene cristata</em> Bouvier, 1911 have been studied and described for the first time by the methods of light (LM) and scanning electron microscopy (SEM). The main morphometry parameters have been determined in larvae and adult egg-bearing males. The general plan of the postlarvae is presented together with its specific features. The postlarvae of the studied <em>Austropallene</em> species combine the features of lecithotrophic and free-living pycnogonid larvae. The diversity of larvae in the Nymphonoidea superfamily has been analysed considering original and published data, and a morphological series has been developed. The complex of lecithotrophic larvae, like postlarvae of Callipallenidae, should be considered as primary for the entire superfamily. It is also suggested that sea spiders with lecithotrophic larvae tend to follow the K-strategy, but they care for their offspring to varying degrees.</div></div>","PeriodicalId":55461,"journal":{"name":"Arthropod Structure & Development","volume":"83 ","pages":"Article 101395"},"PeriodicalIF":1.7,"publicationDate":"2024-10-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142481641","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-09-01DOI: 10.1016/j.asd.2024.101383
Wan-Ruo Ma, Lu Liu, Ge Wang, Jia-Li Bai, Bao-Zhen Hua
The rectum is an important part of the alimentary canal responsible for ion and water reabsorption of insects. However, it has rarely been studied in the larvae of Panorpidae, the largest family in Mecoptera. Here, we investigated the ultrastructure of larval rectum of the scorpionfly Panorpa liui Hua, 1997 using light and transmission electron microscopy. The rectum comprises tracheal muscular layers, connective tissue, non-cellular basal lamina, junctional cells, rectal epithelium, cuticle with irregular outlines, and a central lumen. The rectal epithelium is infolded to form six longitudinal rectal folds, which are distinct from rectal pads or papillae. In each rectal fold, the apical and basal plasma membranes of epithelial cells are infolded and the lateral plasma membranes form septate and scalariform junctions. The well-developed rectal folds are postulated to be closely associated with reabsorption of ions and water in the larvae. The associations of rectal folds with larval behaviors are briefly discussed in Mecoptera.
{"title":"Ultrastructure of the larval rectum of the scorpionfly Panorpa liui (Mecoptera: Panorpidae)","authors":"Wan-Ruo Ma, Lu Liu, Ge Wang, Jia-Li Bai, Bao-Zhen Hua","doi":"10.1016/j.asd.2024.101383","DOIUrl":"10.1016/j.asd.2024.101383","url":null,"abstract":"<div><p>The rectum is an important part of the alimentary canal responsible for ion and water reabsorption of insects. However, it has rarely been studied in the larvae of Panorpidae, the largest family in Mecoptera. Here, we investigated the ultrastructure of larval rectum of the scorpionfly <em>Panorpa liui</em> Hua, 1997 using light and transmission electron microscopy. The rectum comprises tracheal muscular layers, connective tissue, non-cellular basal lamina, junctional cells, rectal epithelium, cuticle with irregular outlines, and a central lumen. The rectal epithelium is infolded to form six longitudinal rectal folds, which are distinct from rectal pads or papillae. In each rectal fold, the apical and basal plasma membranes of epithelial cells are infolded and the lateral plasma membranes form septate and scalariform junctions. The well-developed rectal folds are postulated to be closely associated with reabsorption of ions and water in the larvae. The associations of rectal folds with larval behaviors are briefly discussed in Mecoptera.</p></div>","PeriodicalId":55461,"journal":{"name":"Arthropod Structure & Development","volume":"82 ","pages":"Article 101383"},"PeriodicalIF":1.7,"publicationDate":"2024-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142146959","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-09-01DOI: 10.1016/j.asd.2024.101382
Martina Lento , Maria Luigia Vommaro , Simone Flaminio , Pietro Brandmayr , Anita Giglio
Solitary bees play a crucial role in ecological systems, contributing to the pollination of crops and wild plants. All females are reproductive, and their habitat requirements include nesting sites, food resources and nesting materials. Although these activities require the ability to detect biotic and abiotic stimuli in the environment, the sensory system of these species is poorly studied. In this study, the antennal sensilla of five solitary bee species belonging to three Apoidea families were investigated using scanning electron microscopy. These included two species of stem-nesting bees, Ceratina cucurbitina (Rossi, 1792) (Apidae) and Osmia scutellaris (Morawitz, 1868) (Megachilidae), and three species of ground-nesting bees, Lasioglossum brevicorne (Schenck, 1870), Lasioglossum leucozonium (Schrank, 1781), and Lasioglossum villosulum (Kirby, 1802) (Halictidae). Thirteen different types of antennal sensilla were identified in females based on their morphological characteristics: sensilla trichodea (subtypes STI, II, III), chaetica (subtypes SchI, II), basiconica (subtypes SBI, II, III, IV), placodea, campaniformia, coeloconica, and ampullacea. Their functional role was discussed and morphology was compared among the species and within the antennal segments in each species. The results provide a baseline for further physiological and behavioural studies to determine the role of antennal sensilla in habitat selection, food search and nesting site selection.
{"title":"Morphology and distribution of antennal sensilla in five species of solitary bees (Hymenoptera, Apoidea)","authors":"Martina Lento , Maria Luigia Vommaro , Simone Flaminio , Pietro Brandmayr , Anita Giglio","doi":"10.1016/j.asd.2024.101382","DOIUrl":"10.1016/j.asd.2024.101382","url":null,"abstract":"<div><p>Solitary bees play a crucial role in ecological systems, contributing to the pollination of crops and wild plants. All females are reproductive, and their habitat requirements include nesting sites, food resources and nesting materials. Although these activities require the ability to detect biotic and abiotic stimuli in the environment, the sensory system of these species is poorly studied. In this study, the antennal sensilla of five solitary bee species belonging to three Apoidea families were investigated using scanning electron microscopy. These included two species of stem-nesting bees, <em>Ceratina cucurbitina</em> (Rossi, 1792) (Apidae) and <em>Osmia scutellaris</em> (Morawitz, 1868) (Megachilidae), and three species of ground-nesting bees, <em>Lasioglossum brevicorne</em> (Schenck, 1870), <em>Lasioglossum leucozonium</em> (Schrank, 1781), and <em>Lasioglossum villosulum</em> (Kirby, 1802) (Halictidae). Thirteen different types of antennal sensilla were identified in females based on their morphological characteristics: sensilla trichodea (subtypes STI, II, III), chaetica (subtypes SchI, II), basiconica (subtypes SBI, II, III, IV), placodea, campaniformia, coeloconica, and ampullacea. Their functional role was discussed and morphology was compared among the species and within the antennal segments in each species. The results provide a baseline for further physiological and behavioural studies to determine the role of antennal sensilla in habitat selection, food search and nesting site selection.</p></div>","PeriodicalId":55461,"journal":{"name":"Arthropod Structure & Development","volume":"82 ","pages":"Article 101382"},"PeriodicalIF":1.7,"publicationDate":"2024-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142146958","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}