Observations on the buccal capsule and associated glands of adult Bunostomum trigonocephalum (nematoda)

Wilfred M. and Lee D. L. 1981. Observations on the buccal capsule and associated glands of adult Bunostomum trigonocephalum (Nematoda). International Journal for Parasitology11: 485–492. The buccal capsule or stoma of Bunostomum trigonocephalum is a large, cuticular-lined structure. The head of the nematode lacks distinct lips and has a large ovoid mouth which is partly occluded by a pair of sub-ventral cuticular plates which arise from the wall of the buccal cavity. A pair of sub-ventral lancets or basal onchia are situated at the base of the buccal cavity and a dorsal tooth arises from the base of the buccal cavity and extends forwards to terminate just inside the mouth. A duct lies within this dorsal tooth and extends from the ampulla of the dorsal oesophageal gland at the base of the tooth to open on the dorsal side of the tooth just below its sharp tip. A pair of muscles extends from the dorsal surface of the oesophagus to the base of the buccal capsule and are thought to bring about jerking movements of the head. Non-specific esterase and small amounts of acid phosphatase were detected in the oesophageal glands. Non-specific esterase and cholinesterase were detected in the large amphidial glands but not in the excretory glands. The possible role of the various structures and enzymes during feeding is discussed.     

The ultrastructure of the alimentary tract of the skin-penetrating larva of Nippostrongylus brasiliensis (Nematoda)

The structure of the alimentary tract of the third stage infective larva of Nippostrongylus brasiliensis has been described. The cuticle which lines the buccal cavity and oesophagus differs from that which lines the mouth and covers the external surface of the nematode. The oesophagus is a cellular structure and is not, as previously thought, a syncytium. The secretory granules of the oesophageal glands are surrounded by multi-layered membranes which give a myelinated appearance to the granules. The cells of the oesophago-intestinal junction are lined with cuticle and are presumably part of the stomodaeum. The intestine is thin-walled and the cells bear short, widely spaced microvilli. The lumen of the intestine contains whorls of membranes which are probably phospholipid and could act as a food reserve for the larva. The rectum and anus are lined with cuticle.     

Ultrastructure of the anterior alimentary tract of a monogenean, Diclidophora merlangi

The anterior alimentary tract of Diclidophora merlangi is composed of a complex series of morphologically distinct epithelia interconnected by septate desmosomes and penetrated by the openings of numerous unicellular glands. The mouth and buccal cavity are lined by an infolding of modified body tegument, distinguished by uniciliate sense receptors, buccal gland openings, and in the buccal region by a dense, spiny appearance. The prepharynx is covered by an irregularly folded epithelium and, for part of its length, by the luminal cytoplasm of the prepharyngeal gland cells. The epithelium is syncytial and pleiomorphic, and regional variation in structure is common. A separate epithelium invests the lips of the pharynx and its free surface is greatly amplified by numerous, dense lamellae of varying dimensions. The lip epithelium is continuous with cytoplasmic processes of cells located external to the pharynx. A further, distinct epithelium borders the pharynx lumen and is composed of discrete cytoplasmic units connected by short septate desmosomes. The oesophagus is lined by a modified caecal epithelium, lacking haematin cells, and, in places, is perforated by the openings of oesophageal gland cells; it is continuous with the syncytial connecting tissue of the gut caeca.     

Ultrastructure of the Feeding Apparatus of Rhabdodemania minima Chitwood, 1936 (Enoplida: Rhabdodemaniidae)

The feeding apparatus of the marine nematode Rhabdodemania minima Chitwood, 1936 has been examined with light and transmission electron microscopy. The buccal capsule consists of a posterior region with smooth walls bearing three sets of three minute denticles at its posterior end and three large onchia in its mid region; a middle region with grooved walls; and an anterior region with costae and six odontia. The anterior and middle portions of the buccal capsule are enveloped by the cephalic cuticle, whereas the posterior region, which is set off from the middle region by a buccal seam, is partially enveloped by the anterior end of the esophagus. Two subventral esophageal glands open into the lumen of the esophagus. Secretions of each of three paraesophageal glands are conveyed through a duct in each of the three corresponding corners of the buccal wall to an opening between labia. A pair of wing-like thickenings, termed pterons, embraces the duct of each paraesophageal gland in the posterior and middle regions of the buccal capsule. A model of how the buccal capsule operates is proposed and tested. Morphological and functional aspects of the buccal apparatus and cephalic cuticle are compared with those of other taxa of the Enoplida, and their phylogenetic implications are discussed.     

Ultrastructural aspects of the oesophageal and reproductive systems of the equine parasite Strongylus vulgaris

The ultrastructure of the dorsal oesophageal gland ampulla and its relationship with the oesophagus, oesophageal ultrastructure, and control mechanisms in oesophageal activity were studied. Terminal ducts of the sub-ventral glands open through the oesophageal crown at the base of the buccal cavity. The terminal duct of the dorsal oesophageal gland running through the dorsal gutter opens to the exterior at the rim 'groove' of the buccal capsule. The posterior oesophageal region is clavate and the cuticle of the lumen folds to form outlet valves, 'valvulae'. An inconspicuous oesophago-intestinal valve (three lobes) connects oesophagus and intestine and is visualized in the open and shut position. In the female reproductive tract, with the exception of the uterus, the cells lie on a thick, irregular (convoluted) basal lamina. The apical plasma membrane of the uterus, and seminal receptacle, extend into the lumen by microvilli-like projections with which spermatozoa make intimate contact. The lumen of the uterus is filled with oocytes, fertilized and unfertilized. Testicular cells have two parts linked by a rachis. Spermatocytes are elongated with a large nucleus, distinct nuclear membrane, and many granules. The apical membrane of the rachis forms long microvilli-like projections with balloon-like tips. The amoeboid spermatozoa contain membrane specializations, a nucleus devoid of a membrane, and are enclosed by a pseudopodial-like extension.     

Development and evolution of adult feeding structures in Caenogastropods: overcoming larval functional constraints

SUMMARY Comparative study of the developing foregut in three species of caenogastropods, including an herbivorous grazer ( Lacuna vincta ) and two carnivores ( Euspira [ Polinices ] lewisii and Nassarius mendicus ), suggests how the specialized adult foregut of a carnivorous neogastropod evolved within a life cycle having a planktotrophic larva. Postmetamorphic feeding structures (buccal cavity and radular sac) in all three species achieve advanced differentiation in the larval stage, permitting juvenile feeding at 3 days postmetamorphosis. Recent phylogenetic hypotheses for the Gastropoda predict that foregut developmental patterns in E. lewisii and N. mendicus are derived, relative to that of L. vincta. In hatching larvae of these three, the anlage of postmetamorphic feeding structures is a small patch of nonciliated cells embedded in the ventral wall of the larval foregut and the patch soon forms an outpocketing. During subsequent morphogenesis, Euspira lewisii and N. mendicus share a developmental novelty that involves semi-isolation of the developing, postmetamorphic buccal cavity and radular sac from the larval foregut and formation of a new, definitive mouth at metamorphosis. Nassarius mendicus , a neogastropod, embellishes this novelty by adding the entire anterior esophagus and valve of Leiblein ( de novo structures) to the semi-isolated buccal cavity. Therefore, a valve and long stretch of muscular anterior esophagus, which are necessary for feeding with a pleurembolic proboscis, are preformed in the larval stage of this neogastropod without interfering with larval feeding. The inferred evolutionary events leading to postmetamorphic feeding specialization in N. mendicus are invisible in adults; they require reconstruction from comparative developmental analysis.     

Homology conundrum among foreguts of caenogastropod molluscs: A view from comparative patterns of development

Evolution of two novel feeding strategies among caenogastropod molluscs, suspension feeding in calyptraeids such as Crepidula fornicata and predatory feeding with a pleurembolic proboscis among neogastropods, may have both involved elongation of the anterior esophagus. Emergence of predatory feeding with a proboscis is particularly significant because it correlates with the rapid adaptive radiation of buccinoidean and muricoidean neogastropods during the Cretaceous. However, the notion that this important evolutionary transition involved elongation of the anterior esophagus to extend down a long proboscis has been disputed by evidence that it may have been the wall of the buccal cavity that elongated. We undertook a comparative study on foregut morphogenesis during larval and metamorphic development in C. fornicata and in three species of neogastropods with a pleurembolic proboscis to examine the hypothesis that the same region of foregut has elongated in all. We approached this by identifying a conserved marker for the boundary between buccal cavity and anterior esophagus, which was recognizable before the developing foregut showed regional differences in length. A survey of four species of littorinimorph caenogastropods suggested that the site of neurogenic placodes for the buccal ganglia could serve as this marker. Results showed that foregut lengthening in C. fornicata involved elongation posterior to neurogenic placodes for buccal ganglia, an area that corresponded to the anterior esophagus in the other littorinimorphs. However, foregut elongation occurred anterior to neurogenic placodes for buccal ganglia in two buccinoidean and one muricoidean neogastropod. The elongated foregut within the pleurembolic proboscis of these neogastropods qualifies as anterior esophagus only if the definition of the anterior esophagus is expanded to include the dorsal folds that run down the roof of the buccal cavity. Regardless of how the anterior esophagus is defined, comparative developmental data do not support the hypothesis of homology between the elongated adult foregut regions in C. fornicata and in neogastropods with a pleurembolic proboscis.     

The Buccal Organ of Some Monogenea Polyopisthocotylea

Light and electron microscopic studies of the 'buccal suckers' of Gotocotyla secunda showed that they are complex structures with muscular, glandular, (resorptive?), and probably sensory components. The name 'buccal organ' is therefore proposed for them. Ducts run from the lumen of the buccal organs to their dorsal, ventral and lateral surface and communicate with lacunae surrounding them. The surface of the ducts and of the muscular walls of the buccal organs are lined by tegument with short microvilli, tegument with dense, long surface lamellae, and tegument with thick, long microvilli which have an electron-dense core. The latter type of tegument contains many vesicles and electrondense ovoid bodies, and is traversed by gland ducts containing large secretory droplets. Electron microscopic examination showed that the prebuccal convoluted structures in Heteromicrocotyloides mirabilis are a modified tegument connected to subtegumental cells. Light microscopic studies of Gotocotyla bivaginalis. Pseudothoracocotyla indica, Pricea multae and Heteromicrocotyla australiensis showed that the first three species have buccal organs similar to those in G. secunda , whereas the last species resembles H. mirabilis. It is tentatively assumed that the buccal organs play a role in finding suitable sites for bloodfeeding.     

Gland cells associated with the alimentary tract of a monogenean, Diclidophora merlangi

Three distinct groups of unicellular glands open into the buccal cavity, prepharynx, and oesophagus, respectively, of Diclidophora merlangi. Buccal glands produce a dense, acidophilic secretion of protein-rich droplets that are discharged from duct-like extensions of the glands by eccrine secretion. Prepharyngeal glands are extensive and contain basiphilic secretory droplets of varying density and characterized by the presence of one or two dense core-like inclusions. The droplets are PAS-positive and reactive for protein, and accumulate in the gland cell apices which form part of the lining to the prepharynx lumen. They are released in large numbers by apocrine secretion or, individually, by an eccrine secretory mechanism. Oesophageal glands are acidophilic and contain electronlucid, PAS-positive droplets that develop a crystalline appearance prior to release via either eccrine or apocrine secretion. Differences in ultrastructure and histochemistry indicate the glands are also functionally separate, and their probable role in feeding and extracellular digestion of blood in the worm is discussed.     

The anterior glands of adult Necator americanus (Nematoda: Strongyloidea)—I Ultrastructural studies

The ultrastructure of the amphidial, oesophageal and excretory glands of N. americanus is described. There are two amphidial glands, and each is attached to a lateral hypodermal cord. Anteriorly the glands become associated with the amphidial sense organs. The amphidial glands synthesize complex secretion granules which appear to release their contents into the sense organ. Secretions thus pass over the amphidial cilia and exit via the amphidial pore. It is suggested that the secretory activity of these glands is under direct nervous control. There are three oesophageal glands, and each synthesizes dense secretion granules. The secretions of the oesophageal glands are released into the lumen of the oesophagus and into the buccal capsule. The two excretory glands are ventral in position and connected to the tubular excretory system. These glands synthesize secretion granules of varying density. Secretions from the excretory glands may exit via the excretory pore, or pass back into the tubular excretory system, or both.     

New buccinator myomucosal island flap: anatomic study and clinical application

The authors studied the vascular anatomy of the buccinator muscle by dissecting fresh cadavers. The anatomy of the buccal branches of the facial artery consistently confirmed the existence of a posterior buccal branch, a few inferior buccal branches, and anterior buccal branches to the posterior, inferior, and anterior portions of the buccinator. The buccal artery and posterior buccal branch anastomose to each other and ramify over the muscle. Several veins originate from the lateral aspect of the muscle, converge into the buccal venous plexus, and drain into the facial vein (from two to four tributaries) or into the pterygoid plexus and the internal maxillary vein (from the buccal vein). These vessels and nerves enter the posterior half of the buccinator posterolaterally. The facial artery and vein are located at variable distances from each other around the oral commissure and the nasal base. Two patterns of buccinator musculomucosal island flaps supplied by these buccal arterial branches are proposed in this article. The buccal musculomucosal neurovascular island flap (posteriorly based), supplied by the buccal artery, its posterior buccal branch, and the long buccal nerve, can be passed through a tunnel under the pterygomandibular ligament for closure of mucosal defects in the palate, pharyngeal sites, the alveolus, and the floor of the mouth. The buccal musculomucosal reversed-flow arterial island flap (superiorly based), supplied by the distal portion of the facial artery through the anterior buccal branches, can be used to close mucosal defects in the anterior hard palate, alveolus, maxillary antrum, nasal floor and septum, lip, and orbit. The authors have used the flaps in 12 patients. There has been no flap necrosis, and results have been satisfactory, both aesthetically and functionally.     

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.     

Food selection and consumption by estuarine nematodes

Summary The feeding strategies and feeding techniques of 12 nematode species, isolated from the Ems-Dollard estuary, were investigated in agar cultures. In the consumption of bacteria, algae, diatoms, protozoa and small metazoa, two main strategies are distinghuished: the non-selective strategy, characteristic of species living on the surface of macrophytes, and the selective strategy, characteristic of sediment-inhabiting species. The selective strategists showed various ingestion techniques, depending on the size and armature of the buccal cavity; food items could be ingested whole, or pierced or cracked and the contents sucked out.Publication No. A 73 of the project Biological Research in the Ems-Dollard estuary.     

Oesophageal transit of six commonly used tablets and capsules.

The oesophageal transit of six commonly used tablets and capsules containing barium sulphate was evaluated radiologically using fluoroscopy in 121 healthy volunteers. To determine the influence of the subject''s position and the amount of water taken each subject swallowed three preparations while recumbent and standing and with 25 ml or 100 ml of water. Failure of swallowing (defined as oesophageal transit taking more than 90 seconds) occurred in 22% of 726 swallowings, but globus was complained of in only 33% of these. Sixty per cent of the volunteers had difficulty in taking one or more of the preparations. Many preparations adhered to the oesophageal membrane and started to disintegrate in the lower part of oesophagus. It is recommended that subjects should remain standing for at least 90 seconds after taking capsules or tablets and that all preparations should be taken with at least 100 ml of water. Small tablets are swallowed most easily. Liquid forms of medication (suspensions) should be considered for bedridden patients and those who have difficulty in swallowing.     

Smelling Behaviour of Urodele Amphibians in an Aquatic Environment: Study in Pleurodeles waltl.

In urodele amphibians, the olfactory input is important in the triggering and controlling of sexual and feeding behaviours. In an aquatic environment, a water sample is drawn through the nostrils to the olfactory organs. This sampling consists of the following acts: the buccal floor is pressed down by the action of the tongue muscles and skeleton, the consequence of which is the transmission of a depression to the olfactory chambers via the choanas; water is then aspirated and flows over the sensory areas of the olfactory mucosa before entering the buccal cavity via the choanas; water is finally expelled in front of the animal, the opening of the jaws being synchronous to a fast upward movement of the buccal floor. A thermistor telemetry technique enabled us to show a relationship between smelling behaviour and feeding behaviour, particularly variations in intensity and frequency of smelling behaviour related to the chemical qualities of the surroundings.     

Previously unrecognized stages of species‐specific colonization in the mutualism between Xenorhabdus bacteria and Steinernema nematodes

The specificity of a horizontally transmitted microbial symbiosis is often defined by molecular communication between host and microbe during initial engagement, which can occur in discrete stages. In the symbiosis between Steinernema nematodes and Xenorhabdus bacteria, previous investigations focused on bacterial colonization of the intestinal lumen (receptacle) of the nematode infective juvenile (IJ), as this was the only known persistent, intimate and species‐specific contact between the two. Here we show that bacteria colonize the anterior intestinal cells of other nematode developmental stages in a species‐specific manner. Also, we describe three processes that only occur in juveniles that are destined to become IJs. First, a few bacterial cells colonize the nematode pharyngeal‐intestinal valve (PIV) anterior to the intestinal epithelium. Second, the nematode intestine constricts while bacteria initially remain in the PIV. Third, anterior intestinal constriction relaxes and colonizing bacteria occupy the receptacle. At each stage, colonization requires X. nematophila symbiosis region 1 (SR1) genes and is species‐specific: X. szentirmaii, which naturally lacks SR1, does not colonize unless SR1 is ectopically expressed. These findings reveal new aspects of Xenorhabdus bacteria interactions with and transmission by theirSteinernema nematode hosts, and demonstrate that bacterial SR1 genes aid in colonizing nematode epithelial surfaces.