The ultrastructure of the female accessory gland,the cement gland,in the insect Rhodnius prolixus

The cement gland of Rhodnius prolixus is an epidermally derived tubular gland consisting of a distal synthetic region and a proximal muscular duct region. The synthetic region consists of numerous secretory units joined to a central chitinous duct via cuticular ductules. Proteinaceous secretion, synthesized by the goblet-shaped secretory cell, passes through the delicate cuticular lattice of a ductule-end apparatus and out through fine ductules to the central duct. Secretory cells are rich in rough endoplasmic reticulum and mitochondria. Light microscopy, SEM and TEM reveal the delicate lattice-like end apparatus structure, its formation and relationship to the secretory cell. The secretory cell associates via septate junctions with a tubular ductule cell that encloses a cuticle-lined ductule by forming an elaborate septate junction with itself. The ductules are continuous with the cuticle lining of the large central duct that conveys secretion to the proximal area. The proximal muscular duct has a corrugated cuticular lining, a thin epithelium rich in microtubules and thick longitudinal, striated muscles which contract during oviposition, forcing the secretion out. Histochemistry and electrophoresis reveal the secretion as proteinaceous.     

Morphology and ultrastructure of the Dufour gland in workers of social wasps (Hymenoptera, Vespidae)

The Dufour gland in workers of vespine wasps appears as an unpaired tubiform gland that opens in close proximity to the sting base. The epithelial cells that line the central reservoir are characterized by apical microvillus-like projections and deep basal invaginations. Their cytoplasm contains a well-developed Golgi apparatus, numerous mitochondria, as well as strands of smooth endoplasmic reticulum. The Dufour gland duct occurs ventrally to the venom gland duct, and bends downward near the sting base to open in the dorsal vaginal wall. In this region, the duct is dorsoventrally flattened, and shows conspicuous bundles of parallel microtubules in the epithelial cells, that transmit the pulling forces of the myofilaments of the underlying muscular supply to the cuticle. This results in an active opening mechanism regulated by muscular contraction, while passive closure probably results from the return of the cuticular intima to a rest position.     

Ultrastructure of the excretory duct in the silk gland of the sugarcane borer Diatraea saccharalis (Lepidoptera: Pyralidae)

The excretory duct in the silk gland of the sugarcane borer Diatraea saccharalis consists of two morphologically distinct regions, recognized by scanning and transmission electron microscopy. The thin posterior region, adjacent to the glandular region, presents a regular surface. Secretory vesicles containing either electron-dense or fibrillar cuticular-like materials are observed in their apical cytoplasm; the same cuticular materials were detected as extracellular deposits among the microvilli. The short anterior region, near the common duct, exhibits surface protrusions; there are no secretory vesicles in their apical cytoplasm. These results show that only the duct cells at the posterior region are involved in the secretion of the cuticular intima elements. Desmosome-like structures were visualized linking together adjacent microvillar membranes only in the cells of anterior duct region, with unknown function. The transition between the duct and the glandular region is abrupt; the cells of the glandular and posterior duct regions present large amounts of microtubules. Nerve fibers can be observed between the duct cells in their two regions, suggesting that control of silk secretion may occur in the excretory duct via neurotransmitter liberation.     

Functional morphology and neuronal innervation of the prothoracic defence gland in Timema

Timema is the most basal genus of Phasmatodea and the sister group to the remaining stick and leaf-insects (Euphasmatodea). An autapomorphy of all phasmids is the paired prothoracic exocrine defence glands. In this study, the anatomy and innervation of the defence glands in Timema petita and Timema chumash are described and compared with the data on Euphasmatodea. In all phasmids, the glands consist of a cuticular epithelium, a secretory epithelium and muscular fibres that compress the lumen. In Timematodea, the muscular part of the gland is less developed than in Euphasmatodea and the ejection of the defence secretion depends on the dorsal longitudinal neck muscles. On the neuroanatomical level, Timema petita and Timema chumash lack neurons that are involved in the independent contraction of the gland in euphasmids. In both studied species of Timema, neck muscles play an active role in the gland function which is not observed in any other phasmid. Considering the basal position of this genus, this supports the hypothesis that in euphasmids, the muscular part of the gland evolved from the dorsal longitudinal neck muscles. Additionally, the same nerves that innervate the dorsal longitudinal neck muscles in all Polyneoptera also innervate the defence glands in phasmids.     

Ejaculatory duct of the migratory grasshopper,Melanoplus sanguinipes (fabr.) (Orthoptera : Acrididae): A histological and ultrastructural analysis

The ejaculatory duct of the migratory grasshopper (Melanoplus sanguinipes [Fabr.]) (Orthoptera : Acrididae) is divisible into 3 regions: upper ejaculatory duct (UED) into whose anterior end the accessory glands and vasa deferentia empty; the funnel characterized by its slit-like lumen; and the lower ejaculatory duct (LED). Anteriorly, the UED has a keyhole-shaped lumen surrounded by a thin intima and highly columnar epithelial cells whose most conspicuous feature is massive aggregations of microtubules. More posteriorly, the UED lumen differentiates into dorsal and ventral chambers, the former having a thick cuticular lining armed with spines. In the hindmost part of the UED, the ventral chamber expands to obliterate the dorsal chamber; its cuticular lining thickens, and conspicuous lateral evaginations develop. The thick cuticle includes 3 distinct layers and on its surface carries numerous spatulate processes. In this region, the epithelial cells develop numerous short microvilli beneath which are many mitochondria. As the funnel is reached, the intima becomes extremely thick, and the epithelial cells lack microvilli and most microtubules. Within the funnel, a new, very distinct form of cuticle appears, which is in “units”, each associated with an epithelial cell and having a rounded epicuticular cap. The new cuticle arises ventrally but rapidly spreads to encircle the entire lumen, at which point the LED is considered to begin. Beneath this new cuticle, the epithelial cells are columnar, have long microvilli, numerous mitochondria in the apical cytoplasm, and rough endoplasmic reticulum basally. Apically, adjacent cells are tightly apposed; however, prominent intercellular channels develop more basally. The ejaculatory duct's features are briefly discussed in terms of its role in spermatophore formation.     

宽翅曲背蝗受精囊形态与超微结构观察

[目的]明确宽翅曲背蝗Pararcyptera microptera meridionalis雌虫受精囊的形态、组织结构与超微结构,为更好地认识昆虫受精囊的功能提供依据.[方法]本研究以宽翅曲背蝗已交配雌成虫为实验材料,利用光学显微镜和透射电子显微镜观察其受精囊的形态、组织结构和超微结构.[结果]宽翅曲背蝗受精囊由一个端囊和一条长的受精囊管组成,端囊用于储存精子.端囊和受精囊管有相似的组织学结构,由外到内依次为肌肉层、基膜、上皮层及表皮内膜.上皮层含上皮细胞、腺细胞和导管细胞3种细胞类型.腺细胞具有一个被有微绒毛的细胞外腔.腺细胞的分泌物经细胞外腔通过分泌导管进入到受精囊腔.分泌导管由导管细胞形成.[结论]在宽翅曲背蝗受精囊的端囊和受精囊管上,内膜和腺细胞的细胞外腔结构均存在差异,由此推测,端囊和受精囊管的功能存在一定差异.上皮细胞的超微结构特点显示上皮细胞具有支持、分泌和吸收的功能.     

Ultrastructure of the salivary glands of the planthopper,peregrinus maidis (ashmead) (Homoptera : Delphacidae)

The principal salivary gland of the planthopper, Peregrinus maidis (Ashmead) (Homoptera : Delphacidae), comprises 8 acini of only 6 ultrastructurally different acinar types. In these acini, secretory cells contain elongated vacuoles partly lined by microvilli and by microtubule bundles. These vacuoles are apparently connected with extracellular canaliculi deeply invaginated into secretory cells. Canaliculi of each acinus lead to a ductule lumen, which is lined with spiral cuticular intima, surrounded by duct cells. Striated muscle fibers, supplied with small nerve axons and tracheoles, are found in various acini of the principal gland, usually around secretory and duct cells.In the accessory salivary gland, the 2 large secretory cells contain no elongated vacuoles or canaliculi invaginations. However, in their central region, apically, these cells border a large microvilli-lined canal with its own canal cells. This canal is apparently connected with the cuticle-lined accessory duct, formed by duct cells. Nerve axons, but no muscle fibers, are found in the accessory gland and its duct. It is suggested that the system for transporting secretory material within acini of the principal gland, is basically different from that within the accessory gland.     

Fine structural aspects of silk secretion in a spider. II. Conduction in the pyriform glands

The excretory duct of pyriform glands in Araneus diadematus is connected to the secretory sac through an intermediary cell ring. Apices of these cells bear thick, long microvilli and cytoplasmic extensions containing microtubules in bundles, some of which are derived from normal basal bodies. These finger-like extensions lie between the cuticular intima and the secretory product; they are thought to protect the intima and to initiate moulding of the silk thread. Structural features of the duct cells suggest that the latter play a role in the control of the water content of the silk glue which is restricted to the last portion of the duct where numerous nerve endings are inserted between cells. It is evident that duct structure and chemical and physical characteristics of silk are correlated in all spider silk glands.     

The male reproductive system of Costelytra zealandica (White)(Coleoptera: Scarabaeidae: Melolonthinae)

Abstract

The morphology and histology of the male internal reproductive organs of Costelytra zealandica show many similarities to other Scarabaeoidae, and are particularly close to other Melolonthinae and to Rutelinae. Testes follicles of C. zealandica have the usual structure for Melolonthinae with basal lobes surrounding the ends of the vasa efferentia. Epithelial cells of the vasa efferentia, vasa deferentia, and vesiculae seminales have similar densely basophilic cytoplasm but muscle layers are best developed around the latter. Accessory glands lack muscle and are not differentiated histologically into regions but do differ from their reservoirs. The ejaculatory duct has a cuticular intima and is differentiated into anterior and posterior regions. Both are surrounded by a muscular sheath which expands in the posterior region to enclose fluid. This forms a hydraulic mechanism for everting the internal sac during intromission. The parameres hook into the female’s genital chamber during copulation and have no pincer action. Probable homologies are listed between muscles of the external genitalia and anus of C. zealandica and other Scarabaeoidea.     

Fine structure of the secretory and sensory organs on the cephalon and the first pereionite of Trichoniscus alexandrae Caruso (Crustacea, Isopoda)

Trichoniscus alexandrae Caruso is a blind troglobiont isopod; males possess secretory and sensory organs on the cephalon and 1st pereionite consisting of cuticular pits hosting a tuft of setae and gland openings. Such organs are absent in females. Three types of cuticular structures have been observed: (a) lamellar setae, which likely play a role in protecting the gland openings and favouring the evaporation of secretions; (b) contact chemoreceptors, each provided with six bipolar sensory cells, a scolopale cell and enveloping cells; (c) a secretory cell complex, consisting of a long cylindrical slender duct-forming cell, with the function of transporting to the cuticular surface a secretion produced by two deeper secretory cells. The duct-forming cell is characterized by the presence of numerous microtubules in its cytoplasm, and is provided with a flattened duct. It is suggested that the secretion produced by the secretory cells could serve for sex-recognition.     

Morphologie et ultrastructure du canal des glandes ampullacées d'Araneus diadematus Clerck (Arachnida,Araneidae)

Résumé Le canal des glandes ampullacées d'Araneus diadematus comprend trois longs segments entourés d'une même gaine conjonctive pluristratifiée et riche en glycogène. La structure générale de ces segments est caractérisée par un épithélium simple reposant sur une lame basale fibrillaire et une intima cuticulaire épaisse. Les cellules épithéliales sont riches en microtubules et leur apex est garni de microvillosités. L'intima cuticulaire comporte une sous-cuticule pourvue de mucopolysaccharides acides, une endocuticule, et une épicuticule de structure classique. L'endocuticule est formée de deux sortes de bandes, en alternance, claires ou denses aux électrons, enroulées en spirale le long du manchon cuticulaire; les bandes denses comprennent un réseau de canalicules contournés et anastomosés; le matériel des bandes claires ne présente pas de structure apparente.Dans la partie proximale du premier segment du canal, les cellules épithéliales sont plus riches en microtubules; les microvillositées apicales sont plus rares; la sous-cuticule disparaît et l'endocuticule, devenue cinq fois plus épaisse que dans les autres segments, est formée, du côté des cellules, d'un réseau à larges mailles présentant une infrastructure canaliculaire, et, du côté de l'épicuticule, d'une zone granulo-fibreuse.La jonction proprement dite du canal et de l'ampoule glandulaire est réalisée grâce à une différenciation de l'épicuticule et des membranes plasmiques des cellules glandulaires proximales.Il est proposé de relier les structures décrites à des fonctions de deux types; la structure du segment proximal du canal serait propre à amortir des déformations consécutives au passage des produits de sécrétion; celle des segments suivants paraît correspondre à des phénomènes d'absorption d'eau qui se produiraient depuis la lumière du canal jusqu'au milieu intérieur de l'araignée.

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Morphology and ultrastructure of the ampullate gland duct in Araneus diadematus clerck (arachnida, araneidae)

Summary The ampullate gland duct in Araneus diadematus consists of three long segments surrounded by the same sheath of multi-layered conjunctival tissue rich in glycogen. The duct segments have a single epithelial layer resting on a fibrillar basement membrane and a thick cuticular intima. The epithelial cells are rich in microtubules and their apices carry microvilli. The cuticular intima consists of an acid-mucopolysaccharide-rich sub-cuticle, an endocuticle, and a classical epicuticle. The endocuticle shows two types of alternating bands, which are electron-dense or clear, and are spirally wound over the length of the cuticular stem. The dense bands contain a network of twisted and anastomosing canaliculi. The clear bands do not show any obvious structural patterns.In the proximal end of the first segment, the epithelial cells are richer in microtubules than in other parts of the duct, the number of apical microvilli decreases, the sub-cuticle disappears, and the endocuticle, which becomes five times thicker than in the other segments, forms a loose network showing an infrastructure of canaliculi towards the cells, and a fibrous, granular zone towards the epicuticle.The actual junction of the duct and the glandular ampulla is effected by a differentiation of the epicuticle and the plasma membranes of the proximal glandular cells.We propose that the structures of the proximal segment of the duct lend themselves to a deformation that follows the passage of secretory products; the structure of the following segments seems to be related to water absorption from the duct lumen towards hemolymph.

Nous sommes reconnaissantes au Dr. M. Gabe des conseils qu'il nous a donnés au cours de la rédaction de ce mémoire.     

Derived morphology in a basal moth: The uniquely specialized sternum V glands of Agathiphaga (Lepidoptera: Agathiphagidae)

The sternum V gland is a notable specialization shared by basal Lepidoptera and most Trichoptera; it is generally present in both sexes or in females only. In both orders the secretory cells usually discharge into a sac-like reservoir from which a duct leads to the opening on sternum V. In contrast, the gland in agathiphagid moths is only present in males and it exhibits several unique specialisations: the glandular portion being the apical (morphologically anterior) part of a long tubular cuticular invagination covered with contiguous ‘type-3’ glandular units; together with the following part of the efferent duct it is coiled like a ball of yarn; the duct expands into a fusiform reservoir, and a separate small sac surrounded by a complex muscular coat is present just inside the gland opening. The principal opener muscle of each gland originates on the contralateral side of sternum VI, hence crossing its counterpart in the midline. Characters of the agathiphagid sternum V gland, the function of which remains unclear (though sex pheromone production may appear most likely), add significantly to the suite of autapomorphies exhibited by this otherwise overall remarkably generalized moth taxon.     

Uropod and lateral plate glands of the terrestrial isopod Porcellio scaber Latr. (Oniscidae,Crustacea): An ultrastructural study

Lateral plate and uropod glands are composed of a binucleated gland cell, a ramified intermediate cell, and an elongated duct cell. The gland cell is divided into several lobes and forms numerous short processes in its periphery. The cytoplasm contains many secretory granules. The granules release their content into the intercellular collecting ducts between the gland cell and the branched extensions of the intermediate cell. The collecting ducts merge into a funnel-shaped space surrounded by the intermediate cell. The duct cell is lined by a cuticular intima and contains long striated bundles of fibrils. The duct cell consists of two different regions. The proximal region is characterized by microvilli on the luminal side and contains many organelles. In the distal region microvilli are lacking and organelles are scarce. Structurally, the uropod and lateral plate glands differ in the number of components within the granules. This is in accordance with the differences in the characteristics of the secretory products of the two gland types. The morphology of the glands, particularly the peripheral position of the collecting system, is unique among exocrine glands of arthropods. J. Morphol. 233:183–193, 1997 © 1997 Wiley-Liss, Inc.     

Fine structural organization of the spermatheca in the cockroach, Periplaneta americana

The detailed structure of the cockroach spermatheca is described and discussed firstly as an example of an insect integumentary gland, and secondly, from the standpoint of its role in reproduction. The gland comprises a cortical rank of separate secretory units, each associated with an epithelial duct cell responsible for receiving secreted materials and transporting them through the cuticular intima lining the reproductive tract. Secretory activity is cyclic, and the probable mode of elaboration and release of secretory material is described, together with the fine structure of the markedly differing intimas associated respectively with the glandular and conducting units.     

The fine structure of the somatic muscles and their attachment to the cuticle in two species of Pycnogonida

The fine structure of the somatic muscles and their attachment to the cuticle in the pyenogonids Nymphon (Chaetonymphon) macronyx G. O. Sars and Boreonymphon cf. abyssorum (Norman) is described. The muscles possess characteristics which are typical of arthropod slow muscle fibers: relatively long sarcomeres, a mean A-band length of about 6 μm and a ratio of thin to thick contractile filaments of 4:1. The sarcotubular system consists of distinct t-tubules, an irregular SR part and randomly distributed dyads and triads, the muscles are attached to the cuticle by specialized epidermal cells containing microtubules extending from the cuticular to the muscular side. The myoepidermal and epidermal-cuticular junctions are described.     

The spermatheca of the Dipsocoridae with special reference to the strange “loculus capsulae” in Harpagospecies (Heteroptera,Dipsocoromorpha)

The spermatheca of Dipsocoridae is described and compared in the three known genera of the family (Cryptostemma, Harpago n. stat. and Pachycoleus); it consists of three distinct parts: a long coiled duct including a short apically differentiated segment (pars intermedialis) of unknown function, a spherical seminal capsule, and a small bulb-shaped apical gland with a muscular pump at its base. The structure of the spermatheca remains very uniform in the family, especially the apical gland that is anatomically distinct from the seminal capsule and which seems to be an apomorphy for the whole Dipsocoromorpha. A recently discovered structure, named here the loculus capsulae, appears to exist only in the two known species of the genus Harpago. This internal cuticular structure is situated on the left side of the seventh tergite. It consists of two broad expansions, extending from the tergite and laterotergite respectively, which maintain the seminal capsule near the abdominal wall. This structure appears as a kind of supporting armature impeding the spherical seminal capsule from free movement in the abdominal cavity. The form and function of this strange structure are discussed in this paper.     

Spermiolytic activity of the epithelium of the spermathecal duct of Rhacocleis annulata fieber (Orthoptera : Tettigoniidae)

This study reports, for the first time, lytic activity in the distal and median regions of the spermathecal duct of Rhacocleis annulata Fieber (Orthoptera: Tettigoniidae). Lysis is more pronounced in recently mated females, and appears to take place in a progressive sequence originating in the cells underlying the cuticular intima. These cells exhibit large heterogeneous vesicles resembling lysosomes, which would participate in the partial dismantling of the cuticular intima. Consequently, the sperm found in the lumen of the latter organ penetrate the cells, probably pushed by the pressure exerted on the luminal walls, and then, together with the cells themselves, undergo lysis. Degradation of spermatozoa seems to follow a strict sequence of events, which ends with the dismantling of the microtubules of the axoneme, as reported previously for Locusta (Cantacuzène, 1971) and for some pulmonate gastropods (Bayne, 1970). We propose that lysis is part of the mechanism dealing with capture and subsequent elimination of surplus sperm transferred to the female during copulation. Accordingly, fertilization activity would occur exclusively within the seminal receptacle. No evidence of a similar phenomenon in the latter organ has previously been reported for Rhacocleis annulata.     

New ultrastructural data from the larva of Paragordius varius (Nematomorpha)

Larvae of Paragordius varius (Leidy, 1851) were investigated using transmission electron microscopy, providing new observations concerning the cuticular structures of the preseptum, the postseptal gland and the pseudointestine. The cuticle is three‐layered but the basal layer is variable in structure. The hooks possess long, intracuticular roots and the stylets have apical teeth. Both postseptal gland and pseudointestine are secretory in function. The postseptal gland is composed of eight cells, which are all connected by a duct leading through the septum into the preseptum. Inside the postseptal gland, the duct wall has numerous pores. The pseudointestine is composed of four cells surrounding a cavity with an amorphous content. A flattened duct within a syncytium with five nuclei leads to a ventral pore close to the posterior end.