Sternal gland structures in males of bean flower thrips,Megalurothrips sjostedti,and Poinsettia thrips,Echinothrips americanus,in comparison with those of western flower thrips,Frankliniella occidentalis (Thysanoptera: Thripidae)

Sternal pores are important features for identification of male thrips, especially within the subfamily Thripinae. They vary in shape, size and distribution even between species of one genus. Their functional role is speculated to be that of sex- and/or aggregation pheromone production. Yet, sexual aggregations are not reported in Echinothrips americanus, known to have sternal pores, while we observed aggregations in Megalurothrips sjostedti, previously reported to lack them.We examined the sternal glands and pores of the thripine species E. americanus and M. sjostedti males, in comparison with those of Frankliniella occidentalis using light microscopy, as well as scanning and transmission electron microscopy. Pore plates of F. occidentalis were ellipsoid and medial on sternites III–VII, while in E. americanus they were distributed as multiple micro pore plates on sternites III–VIII. In M. sjostedti they appeared as an extremely small pore in front of the posterior margin of each of sternites IV–VII. Pore plate and pore plate area were distributed similarly on sternites III–VII in F. occidentalis. However, in E. americanus the total pore plate area increased significantly from sternites III to VIII. Ultrastructure of cells associated with sternal glands showed typical characteristics of gland cells that differ in size, shape and number. The function of sternal glands is further discussed on the basis of morphological comparisons with other thrips species.     

Functional anatomy of oil glands in<Emphasis Type="Italic"> Collohmannia gigantea</Emphasis> (Acari,Oribatida)

Chemical and behavioural studies indicated that the oil glands of the Oribatida represented a central organ for protection and semiochemical communication. The hitherto unknown mode of action of these glands and their microscopic anatomy have been investigated in Collohmannia gigantea by histological and SEM techniques. The paired oil glands are located dorsolaterally in the hysterosoma and mainly comprise large intima-lined and sac-like reservoirs which are surrounded by glandular tissue. The reservoirs consist of a single-layered flat epithelium and probably serve for storage of the oil gland secretion only, but not for its production. Each reservoir opens to the body outside via a single pore. Externally, the pores appear as oval-shaped rings of smooth cuticle, moderately projecting from the surface of the notogaster. The pore orifices are supplied with trapdoor-like closing mechanisms, consisting of cuticular flaps which permit reservoir opening by muscles attaching to the posterior part of the reservoir and the inner side of the notogaster. These morphological data, especially the large intima-lined reservoirs along with closing mechanisms under muscular control, are consistent with supposed biological roles of oil glands as defensive or alarm pheromonal organs.     

La glande sternale dans l'évolution des Termites

Résumé Des différenciations glandulaires de l'épiderme au niveau de certains sternites abdominaux (glandes sternales) existent chez tous les Termites.Mastotermes darwiniensis possède une glande sur chacun des sternites 3, 4 et 5; dans les sous-familles des Stolotermitinæ, Porotermitinæ, Hodotermitinæ, la glande sternale, unique, est située sur le 4^e sternite; tous les autres Termites examinés ont une glande sternale sur le 5^e sternite. Ces glandes existent dans toutes les castes, mais subissent une régression chez les sexués fonctionnels, qu'ils soient imaginaux ou néoténiques.

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Summary Glandular swellings of the epidermis in the region of some abdominal sternites (sternal glands) are always present in Termites.Mastotermes darwiniensis shows 3 glands, one on each of the 3rd, 4th and 5th sternites; in the sub-families Stolotermitinæ, Porotermitinæ and Hodotermitinæ, there is a single sternal gland on the 4th sternite; in all other Termites examined, one finds this sternal gland on the 5th sternite. These glands have been observed in every caste, but they regress in functional reproductives, both imaginal and neoteinic.

     

Fine structure and physicochemical analysis of the metathoracic scent glands of Lincus Malevolus (Rolston) and L. Spurcus (Rolston) (Heteroptera : Pentatomidae)

Bugs of the genus Lincus (Heteroptera : Pentatomidae) are attracted by volatile compounds emitted from the inflorescences of fertile palms. To define the basis of their chemical ecology, we have studied the metathoracic scent glands (MTG) of males and females of 2 species, L. spurcus and L. malevolus. The metathoracic scent gland system belongs to the diastomien type. The 2 glandular pores located between the mesothoracic and metathoracic coxae are associated with “crescent-like” evaporation areas. The large median reservoir, which is composed of one type of flattened pigmented epithelial cells, is flanked by multitubular lateral glands. These glands result from the apposition of 2 cell-type glandular units. The strip-like accessory gland is embedded in the reservoir wall. At its level, the thinner cuticular intima forms finger-like invaginations where a protein secretory product is secreted. Extracts of the volatile fraction of the metathoracic gland secretion were analyzed by capillary gas chromatography (GC) and by GC-mass spectrometry (GC-MS). These analyses exhibited a typical pentatomid MTG composition. The glands of L. spurcus and L. malevolus males and females contain 11 compounds: (E)-2-hexenal, 4-keto-(E)-2-hexenal, (E)-2-hexenoic acid, decane, (E)-2-octenal, undecene, undecane, (E)-2-octenly acetate, (E)-2-decenal, tridecane and (E)-2-decenyl acetate, including 3 major compounds, which represent 60–85% of the secretion in the 2 species: (E)-2-hexenal, (E)-2-octenal, and n-undecane. The 4-keto-(E)-2-hexenal is present only in the L. malevolus MTG, and represents 26% of its secretion. The female extracts of both species are characterized by the presence of (E)-2-hexenoic acid, which was detected in the male extracts as traces.     

Ultrastructure of the wax-gland system in subterranean scale insects (homoptera,coccoidea, margarodidae)

The ultrastructure of wax glands (integumentary, stigmatic, and peristigmatic glands) was investigated in larvae, cysts, and adult females and males of species belonging to the genera Porphyrophora, Sphaeraspis, and Eurhizococcus. The general organization and cytological characteristics are similar for all glands studied. Each gland is composed of a single layer of 8 to 40 cells. The glandular cells are characterized by a very large quantity of smooth endoplasmic reticulum which forms dense zones throughout the cytoplasm, but is always placed near the collecting canals in the presence of mitochondria. Each cell has a central canal reservoir which penetrates it deeply and gives rise to a large number of lateral collecting canals, formed by the invagination of the apical plasma membrane. The canals open into a subcuticular cavity forming a common reservoir in which the secretion is accumulated. This reservoir is covered by a modified cuticle formed from the endocuticle and the epicuticle. The endocuticle is composed of a network of fine tubular structures and has many filaments on its surface. The epicuticle is perforated by numerous pores. There is no cuticular duct. The secretion crosses the cuticle in three successive steps. First, it passes through the filaments, then through fine tubular structures of the endocuticle, and finally through the epicuticular pores.     

An insight into the skin glands,dermal scales and secretions of the caecilian amphibian Ichthyophis beddomei

The caecilian amphibians are richly endowed with cutaneous glands, which produce secretory materials that facilitate survival in the hostile subterranean environment. Although India has a fairly abundant distribution of caecilians, there are only very few studies on their skin and secretion. In this background, the skin of Ichthyophis beddomei from the Western Ghats of Kerala, India, was subjected to light and electron microscopic analyses. There are two types of dermal glands, mucous and granular. The mucous gland has a lumen, which is packed with a mucous. The mucous-producing cells are located around the lumen. In the granular gland, a lumen is absent; the bloated secretory cells, filling the gland, are densely packed with granules of different sizes which are elegantly revealed in TEM. There is a lining of myo-epithelial cells in the peripheral regions of the glands. Small flat disk-like dermal scales, dense with squamulae, are embedded in pockets in the dermis, distributed among the cutaneous glands. 1–4 scales of various sizes are present in each scale pocket. Scanning electron microscopic observation of the skin surface revealed numerous glandular openings. The skin gland secretions, exuded through the pores, contain fatty acids, alcohols, steroid, hydrocarbons, terpene, aldehyde and a few unknown compounds.     

Unusual location and structure of female pheromone glands in Theresimima (= Ino) ampelophaga Bayle-Berelle (Lepidoptera : Zygaenidae)

Morphological and behavioural studies strongly suggest that the sex pheromone glands of female Theresimima (= Ino) ampelophaga (Lepidoptera : Zygaenidae) are situated on the anterior part of the 3rd–5th abdominal tergites. The glandular epithelium consists of 2 cell types: gland cells and wrapping cells. The gland cells have a central microvilli-lined cavity which is in contact with the lumen of the hair. These hairs are exposed during the calling behaviour, and the pheromone is probably given off via pores in the scale wall.     

Ultrastructure of multicellular foregut glands in selected Solenogastres (Mollusca)

Foregut glands in Solenogastres are not only of importance in biological processes like feeding and digestion, but multicellular foregut glands also provide valuable characters for taxonomy and systematics. Here, the fine structure of four different types of foregut glands is investigated: the Meioherpia-type ventrolateral foregut gland of Meioherpia atlantica, the Simrothiella-type ventrolateral foregut gland of Simrothiella cf. margaritacea, and the Pararrhopalia-type ventrolateral foregut gland as well as the dorsal gland of Pararrhopalia pruvoti. Thereby, special focus is set on the arrangement of glandular and supporting cells within the glands, and on the characterization of glandular cells according to the size, shape and electron-density of their secretional vesicles. It is shown that the investigated glands are complex organs composed of non-glandular supporting cells and two to five glandular cell types producing discrete secretions.     

The “rosette-like” structures in the cuticle of Petrobius brevistylis are the openings of epidermal glands

We examined the “rosette-like” structures (RS), found in Archaeognatha and Thysanura, in the compound eyes and the antennae of the machilid Petrobius brevistylis using SEM and TEM. The nature of the RS was unknown until now, and hypothesized to be either a sensillum or the opening of a gland. Our studies show that RS are the orifices of epidermal glands. A gland consists of a single glandular unit of 4 cells: a duct cell, a secretory cell, a ciliary cell and an enveloping cell. The glands are class 3 epidermal glands as defined by Noirot and Quennedey (1974).     

An interommatidial exocrine gland with a “nail-headed” structure in the water strider Aquarius remigis (Hemiptera,Gerridae)

The fine structure of the interommatidial exocrine glands, found in the compound eyes of the water strider Aquarius remigis, is described using light, scanning, and transmission electron microscopy. The glandular pores of the glands are specialized into minute “nail-headed” structures (NS), which are described for the first time in arthropod compound eyes. Each NS is composed of two components: a rod-like stalk and a cup-like depression. The TEM study shows that the glands are class 3 epidermal glands as defined by Noirot and Quennedey (1974, 1991). Each gland consists of 3 cells: a gland cell, an intermediary cell, and a duct (canal) cell. The gland cell contains abundant electron-lucent vesicles, while the intermediary cell contains a large number of osmiophilic secretory granules. These two cells might secrete different substances which mix together in the dilated sac-like portion of the conducting canal before final release. The possible functions of the secretions released from these glands are discussed.     

Comparative investigation of the genital systems in the Opisthobranchia (Mollusca, Gastropoda) with special emphasis on the nidamental glandular system

The reproductive systems and especially the nidamental glands of 20 species of Opisthobranchia belonging to the ”Cephalaspidea s. l.”, Anaspidea, Sacoglossa, Tylodinoidea and Pleurobranchoidea, have been investigated histologically and ultrastructurally. The nidamental glandular system is responsible for the formation of the egg masses. In all investigated species it is divided into three distinct parts. The most proximal part can be an albumen gland (some ”Cephalaspidea s. l.”, Anaspidea and Sacoglossa) or can exhibit a capsule gland (some ”Cephalaspidea s. l.”, Tylodinoidea and Pleurobranchoidea). All species additionally possess a membrane gland and a distally lying mucous gland. In some species the most distal part of the oviduct was also found to be glandular. The structure of the nidamental glands is described and compared within the Opisthobranchia. Albumen and capsule glands are found to be homologous glandular parts of the system. It can be concluded that the albumen gland has undergone a structural and functional change within the evolution of the Opisthobranchia. Accepted: 26 December 2000     

Generation gland morphology in cordylid lizards: An evolutionary perspective

To elucidate the functional significance of the three distinct types of generation glands that have been identified among cordylid lizards, we mapped gland type to the terminal taxa in the most recent phylogenetic tree for the Cordylidae. We used the phylogenetic programme Mesquite and applied the principle of parsimony to infer character states for the ancestral nodes in the tree. For those species where information on gland type was not available from the literature, we conducted a histological investigation of generation gland morphology, using standard histological techniques. We included two species of the sister family Gerrhosauridae in the analysis to serve as outgroups. In both Gerrhosaurus typicus and G. flavigularis, scales immediately anterior to the femoral pores displayed glandular activity, but differed from generation glands of cordylids in the absence of mature glandular generations. Among the cordylids investigated, we identified a fourth type of generation gland in Pseudocordylus subviridis, P. spinosus, and in the two Hemicordylus species, one where the glands consistently comprise of two mature glandular generations. In H. capensis, both single‐ and two‐layer type glands are present. Our reconstruction of ancestral character states suggests a minimum of six transformations from one gland type to another during the evolutionary history of the family. The reconstruction furthermore suggests that the single‐layer type gland reappeared at least once (in Hemicordylus) in the Cordylinae after having been lost. The reconstruction also unequivocally shows that the pit‐like multiple‐layer type gland evolved directly from the single‐layer type and not from the protruding multiple‐layer type. The two‐layer type gland appears to be an intermediary condition between the multiple‐layer and single‐layer types. The evolutionary transformation of generation gland type appears to be linked to changes in lifestyle and associated changes in degree of territoriality and the need for chemical communication. J. Morphol. 275:456–464, 2014. © 2013 Wiley Periodicals, Inc.     

The identification of a shared immunogen present in the salivary glands and gut of ixodid and argasid ticks

The identification of a 70-kDa immunogen present in salivary gland extracts of several ixodid species, namelyHyalomma truncatum (sweating-sickness-inducing (SS+) and non-inducing (SS-) strains),Hyalomma marginatum. rufipes andRhipicephalus evertsi evertsi, is reported. The immunogen was identified by Western blots using a monoclonal antibody of the IgM isotype directed against a 70-kDa immunogen present in the salivary glands of (SS-) femaleH. truncatum ticks. Cross-reactivity with the gut of unfed adult ixodid ticks,Amblyomma hebraeum, Rhipicephalus simus simus, R. evertsi evertsi, Rhipicentor nuttali, H.m. rufipes, and salivary glands of adult argasid species,Ornithodoros savignyi andOrnithodoros moubata, was demonstrated using ELISA.     

Musculature, nervous system and glands of pregenital abdominal segments of the female of Nomia melanderi Ckll. (Hymenopters, Apoidea)

The gross anatomy of muscles, the topography of nerve tissues, and the histology of the pregenital abdominal glands of Nomia melanderi Ckll. are reported in detail. The movable and fixed points of muscle attachment were utilized in establishing a system of nomenclature for a typical abdominal segment. Names of nervules correspond to those of the tissues they innervate. The points of attachment of muscles of the fifth abdominal segment are essentially the same in both Nomia and Apis, except for the second tergo-sternal muscle which, in Nomia, has shifted its point of movable attachment to the membranous integument in front of the intersegmental membrane gland where it helps in relasing glandular secretion. The general plan of the nerves in the fifth abdominal segment in Nomia is more diffuse than in Apis, but there is no difficulty in establishing homology between the nervules of the two species. A pair of intersegmental stretch organs was found in abdominal segments 3–6. Glands of the sixth intersegmental membrane possess a reservoir with peripheral pouches both of which are absent in those of the fifth. Both types of glands have neither closing nor opening mechanisms, and neither is innervated. Release of glandular secretion is accomplished by the action of the tergo-sternal muscles.     

Enhanced Edar Signalling Has Pleiotropic Effects on Craniofacial and Cutaneous Glands

The skin carries a number of appendages, including hair follicles and a range of glands, which develop under the influence of EDAR signalling. A gain of function allele of EDAR is found at high frequency in human populations of East Asia, with genetic evidence suggesting recent positive selection at this locus. The derived EDAR allele, estimated to have reached fixation more than 10,000 years ago, causes thickening of hair fibres, but the full spectrum of phenotypic changes induced by this allele is unknown. We have examined the changes in glandular structure caused by elevation of Edar signalling in a transgenic mouse model. We find that sebaceous and Meibomian glands are enlarged and that salivary and mammary glands are more elaborately branched with increased Edar activity, while the morphology of eccrine sweat and tracheal submucosal glands appears to be unaffected. Similar changes to gland sizes and structures may occur in human populations carrying the derived East Asian EDAR allele. As this allele attained high frequency in an environment that was notably cold and dry, increased glandular secretions could represent a trait that was positively selected to achieve increased lubrication and reduced evaporation from exposed facial structures and upper airways.     

Ultrastructure and cytochemistry of salivary glands of the predator Podisus nigrispinus (Hemiptera: Pentatomidae)

Podisus nigrispinus Dallas (Hemiptera: Pentatomidae) is a zoophytophagous insect with a potential for use as a biological control agent in agriculture because nymphs and adults actively prey on various insects by inserting mouthparts and regurgitating the contents of the salivary glands inside the prey, causing rapid paralysis and death. However, the substances found in saliva of P. nigrispinus that causes the death of the prey are unknown. As a first step to identify the component of the saliva of P. nigrispinus, this study evaluated the ultrastructure and cytochemistry of the salivary glands of P. nigrispinus. The salivary system of P. nigrispinus has a pair of principal salivary glands, which are bilobed with a short anterior lobe and a long posterior lobe, and a pair of tubular accessory glands. The principal gland epithelium is composed of a single layer of cells enclosing a large lumen. Epithelial cells of the principal salivary gland vary from cubic to columnar shape, with one or two spherical and well-developed nuclei. Cells of the anterior lobe of the principal salivary gland have an apical surface with narrow, short, and irregular plasma membrane foldings; apical and perinuclear cytoplasm rich in rough endoplasmic reticulum; and mitochondria with tubular cristae. The basal portion of the secretory cells has mitochondria associated with many basal plasma membrane infoldings that are short but form large extracellular canals. Secretory granules with electron-dense core and electron-transparent peripheral are dispersed throughout the cytoplasm. Cells of the posterior lobe of the principal salivary gland are similar to those of the anterior lobe, except for the presence of mitochondria with transverse cristae. The accessory salivary gland cells are columnar with apical microvilli, have well-developed nucleus and cytoplasm rich in rough endoplasmic reticulum, and have secretory granules. Cytochemical tests showed positive reactions for carbohydrate, protein, and acid phosphatase in different regions of the glandular system. The principal salivary glands of P. nigrispinus do not have muscle cells attached to its wall, suggesting that saliva-releasing mechanism may occurs with the participation of some thorax muscles. The cytochemical and ultrastructural features suggest that the principal and accessory salivary glands play a role in protein synthesis of the saliva.     

Development and Structure of Internal Glands and External Glandular Trichomes in Pogostemon cablin

Pogostemon cablin possesses two morphologically and ontogenetically different types of glandular trichomes, one type of bristle hair on the surfaces of leaves and stems and one type of internal gland inside the leaves and stems. The internal gland originates from elementary meristem and is associated with the biosynthesis of oils present inside the leaves and stems. However, there is little information on mechanism for the oil biosynthesis and secretion inside the leaves and stems. In this study, we identified three kinds of glandular trichome types and two kinds of internal gland in the Pogostemon cablin. The oil secretions from internal glands of stems and leaves contained lipids, flavones and terpenes. Our results indicated that endoplasmic reticulum and plastids and vacuoles are likely involved in the biosynthesis of oils in the internal glands and the synthesized oils are transported from endoplasmic reticulum to the cell wall via connecting endoplasmic reticulum membranes to the plasma membrane. And the comparative analysis of the development, distribution, histochemistry and ultrastructures of the internal and external glands in Pogostemon cablin leads us to propose that the internal gland may be a novel secretory structure which is different from external glands.     

A new species and additional records of Rugilus Leach from Qinling,China (Coleoptera,Staphylinidae, Paederinae)

A new species of Rugilus Leach, Rugilus (Rugilus) huanghaoi sp. n. from Qinling, Shaanxi Province, China, is described and illustrated. Additional records of seven species from Qinling are reported.     

Development of female accessory glands of Chrysomya putoria (Wiedemann) (Diptera: Calliphoridae) during oogenesis

Females of Chrysomya putoria (Diptera: Calliphoridae) have two sexual accessory glands, which are tubular and more dilated at the distal extremity. The glands open independently into the common oviduct. Two morpho-physiological regions were distinguished in the longitudinal semi-thin sections of the glands. The secretory region is constituted by three layers: a cuticular intima, lining the lumen, followed by a layer of small cells, and then a layer of very large secretory cells. The ductal region of the gland presents only two layers: the cuticular intima and a cellular layer. In both regions a basement membrane is present. Each secretory cell has in its apical region a reservoir, which enlarges throughout oogenesis; in its basal region there is a large nucleus. The ductal cells are cylindrical and smaller than the secretory cells. The glandular secretion is synthesized in the cytoplasm of the secretory cells, stored and/or modified in the reservoir, then drained to the lumen through an end apparatus seen in the apical region of the secretory cell. Histochemical tests indicate that this secretion is a glycoprotein. Measurements of the glands from females at different physiological conditions and fed on different diets correlate with the results obtained for changes in the ovary during oogenesis. Cell number averaged 561.2 ± 77.54 per gland. There was no increase in cell number during oogenesis.     

Tarsomere and distal tibial glands: Structure and potential roles in termites (Isoptera: Rhinotermitidae,Termitidae)

Social insects have numerous exocrine glands, but these organs are understudied in termites compared to hymenopterans. The tarsomere and distal tibial glands of the termites Heterotermes tenuis, Coptotermes gestroi and Silvestritermes euamignathus were investigated by scanning and transmission electron microscopy. Pore plates are visible in scanning micrographs on the distal tibial surfaces and on the ventral surface of the first and second tarsomeres of workers of H. tenuis and C. gestroi. In contrast, workers of S. euamignathus have isolated pores spread throughout the ventral surfaces of the first, second, and third tarsomeres and the distal tibia. In all three species each pore corresponds to the opening of a class-3 secretory unit, composed of one secretory and one canal cell. Clusters of class-3 glandular cells are arranged side by side underneath the cuticle. The main characteristics of these exocrine glands include their presence on all the legs and the electron-lucent secretion in the secretory cells. Possible functions of these glands are discussed.