Ultrastructure of Gonionchus australis (Xyalidae,Nematoda)

Observations are reported on the ultrastructure of the buccal cavity, body cuticle, spermatids, spermatozoa, male genitalia, and caudal glands of Gonionchus australis. The buccal cuticle is a continuation of the pharyngeal cuticle. Anteriorly it is secreted by arcade tissue and overlaps the mouth rim; laterally it forms longitudinal tooth ridges. The non-annulated cephalic cuticle differs sharply from the remainder of the body wall cuticle. The cortical and basal zones become much thinner, while a largely structureless, lucent median zone expands to fill the bulk of the lips and lip flaps. Spermatids possess fibrous bodies, multimembrane organelles, mitochondria, and compact chromatin. The spermatozoa of G. australis resemble those of most other nematodes by the absence of the nuclear envelope and presence of fibrous bodies, mitochondria, and compact chromafin. The ejaculatory duct possesses microvilli. Two ejaculatory glands lie beside the duct. Two neurons are located within each spicule and each part of the paired gubernaculum. Caudal gland nuclei are large, with dispersed chromatin. The ducts of all three caudal glands are filled with secretory vesicles.     

Divisispiculimermis mirus n. gen., n. sp. (Mermithidae: Nematoda) Parasitizing Midges in Córdoba,Argentina

Divisispiculimermis mirus n. gen., n. sp., a mermithid parasitizing larvae of Chironomus sp. in the Cajón o Grande Stream, Córdoba, Argentina, is described. The new genus differs from all other mermithid genera in having paired spicules which are separated and divided into proximal and distal sectors. The other diagnostic characters of the genus are medium size, nematodes with the cuticle appearing smooth (lacking cross fibers under the light microscope); head separated from the rest of the body by a slight constriction at the level of the amphids, six cephalic papillae, mouth papillae absent, mouth opening posterior to level of cephalic papillae; six hypodermal chords at midbody; weakly S-shaped vagina; postparasitic juvenile with a tail appendage.     

Stage-specific Differences in Lectin Binding to the Surface of Anguina tritici and Meloidogyne incognita

The occurrence and distribution of several lectin binding sites on the outer surfaces of eggs, preparasitic second-stage juveniles (J2), parasitic second-stage juveniles (PJ2), females, and males of two tylenchid nematodes, Anguina tritici and Meloidogyne incognita race 3, were compared. In both species, a greater variety of lectins bound to the eggs than to other life stages; lectin binding to eggs was also more intense than it was to other life stages. Species-specific differences also occurred. More lectins bound to the amphids or amphidial secretions of M. incognita J2 than to the amphids or amphidial secretions of A. tritici J2. Lectins also bound to the amphids or amphidial secretions of adult male and female A. tritici, but binding to the cuticle occurred only at the head and tail and was not consistent in all specimens. Canavalia ensiformis and Ulex europaeus lectins bound specifically to the outer cuticle of M. incognita. Several other lectins bound nonspecifically. Oxidation of the cuticle with periodate under mild conditions, as well as pretreatment of the nematodes with lipase, markedly increased the binding of lectins to the cuticle of A. tritici J2 but not, in most cases, to M. incognita J2 or eggs of either species.     

Descriptions of Eumonhystera borealis n. sp., Sphaerolaimus occidentalis n. sp., and a Redescription of S. gracilis de Man 1876 (Nemata) from Bothnian Bay,Baltic Sea

The free-living nematodes Eumonhystera borealis n. sp., Sphaerolaimus occidentalis n. sp., and S. gracilis de Man 1876 from Bothnian Bay in the northern Baltic Sea are described and illustrated. Eumonhystera borealis n. sp. differs from other species by its small body size (314-393 μm), narrow body (a = 37-49), and large anterior amphids. In Sphaerolaimus occidentalis n. sp. the amphids are posterior to the buccal cavity, and it differs from other similar species by having two sclerotized rings in the posterior part of the buccal cavity. An intersex is reported for S. gracilis. Sphaerolaimus gracilis is cannibalistic or a predator of other species, with a preference for E. borealis n. sp. Sphaerolaimus occidentalis n. sp. coexists with S. gracilis at depths of 80 m but not at 12 m.     

Deep-sea nematodes from the Indian Ocean: new and known species of the family Comesomatidae

Twelve new and known species of the genera Sabatieria,Cervonema, Paramesonchium, Hopperia and Dorylaimopsis and one new genus, Kenyanema aredescribed from the Indian Ocean and S. pisinna Vitiello,1970 from the Mediterranean Sea. Sabatieria lucia sp. n.is characterised by short but distinct inner and setiformouter labial sensilla and long (4–5 µm or 30–33% hd)cephalic sensilla; S. conicauda Vitiello, 1970, ischaracterised by tiny inner and outer labial sensilla andsetiform cephalic ones and short and thick cylindrical tail;Sabatieria pisinna is characterised by short innerand outer labial sensilla, setiform (3µm long) cephalicsensilla, multispiral amphids with 3.25–3.5 turns and a tailwhich is conical in the anterior 2/3 and posterior 1/3cylindrical; Cervonema tenuicauda Schuurmans Stekhoven,1950, is characterised by anterior sensilla in twocircles which are equal in length (3µm long), multispiralamphids with 3–4 turns and located at 1.5 times hd from theanterior end, simple spicules one abd long and 6–7 fineprecloacal supplements; Cervonema minutus sp. n.characterised by an extremely attenuated anterior end,spiral amphids with 4–5 turns (80–90% cbd) and short,simple spicules (0.8 abd long); Cervonema gourbaulti sp.n. characterised by long (4–5 µm) labialand cephalic sensilla, spiral amphids with 5–6 turns(73–88% cbd) and an elongate crenate terminal pharyngealbulb; Paramesonchium mombasi sp. n. characterised bylong labial (5 µm) and cephalic (21 µm) sensilla thatare close together and wide amphids (80–90% cbd); Kenyanema monorchis gen. et sp. n. characterised bya head region narrower than the rest of the body, fourcephalic sensilla (3 µm long) and spiral amphids with1.5–2 turns; Hopperia indiana sp. n. characterised byshort conical anterior sensilla, arcuatespicules that have a velum and a gubernaculum with a longand sharp pointed apophysis; Dorylaimopsis coomansi sp.n. characterised by long (8–10µm) cephalic setae,cuticular punctation with lateral differention of irregularlyarranged dots at the pharyngeal region and 1–3longitudinal rows of dots posterior of the pharynx; spiculeswith a unique shape; Dorylaimopsis gerardi sp. n.characterised by short setiform labial and long (6–7 µm)cephalic sensilla, punctated cuticle with lateraldifferentiation of irregularly arranged dots at firstthen three or four irregularly arranged longitudinal rows atthe pharyngeal and tail regions and two regularly arrangedlongitudinal rows of dots on the rest of the body, aconico-cylindrical tail with a distinctly swollen tip;Dorylaimopsis variabilis sp. n. is characterised byshort labial and setiform cephalic sensilla (33–58% hd),multispiral amphids with three turns, cuticular punctationswith lateral differentiation of three longitudinalrows at the pharyngeal and tail regions and two longitudinalrows on the rest of the body, spicules that are thin andslightly arcuate. The position of S. pisinna accordingto the grouping of Platt, 1985 of Sabatieriaspp. is also discussed. Kenyanema monorchis representsthe first monorchic species in the family.     

Ultrastructure of introvert and pharynx of Halicryptus spinulosus (priapulida)

The introvert of Halicryptus spinulosus bears three kinds of sensilla: buccal papillae, ordinary scalids, and dentoscalids. They are all characterized by bipolar monociliary receptor cells. The former two have apical openings at which the sensory cilia are in close contact with the ambient sea water. The pharyngeal teeth are composed of slender epithelial cells the tips of which are devoid of organelles and a thick cuticle. The anatomy of the muscle arrangement of the pharynx is described. Glands occur at the junction of the pharynx and midgut.     

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.     

Localization of Cuticular Binding Sites of Concanavalin A on Caenorhabditis elegans and Meloidogyne incognita

Utilizing a Concanavalin A (Con A)-hemocyanin conjugate, the majority of cuticular Con A binding sites were shown to be localized on the head region of Caenorhabclitis elegans and Meloidogyne incognita. Secretions which apparently emanated from the amphids and inner labial papillae did not label.     

First Record of Bourgelatia diducta (Nematoda: Chabertiidae) from Wild Boars in the Republic of Korea

This study describes the first record of Bourgelatia diducta (Nematoda: Chabertiidae) from wild boars in the Republic of Korea (=South Korea). Gastrointestinal tracts of 87 Korean wild boars (Sus scrofa coreanus) hunted in mountains in the south-western part of South Korea between 2009 and 2012 were examined for their visceral helminths. B. diducta, as identified by morphological characteristics of the head and tail, were recovered from the large intestine of 47 (54%) wild boars. The average length of adult female worms was 11.3±0.87 mm and the thickest part of the body measured 0.54±0.04 mm in maximum width, while those of males were 9.8±0.72 and 0.45±0.03 mm, respectively. The characteristic J-shaped type II ovejector was observed in females, and the type II dorsal ray with 2 rami on each side of the median fissure was uniquely seen in males. The buccal capsule was small, relatively thin-walled, cylindrical, very short, and ring-shaped. The externodorsal ray arose from a common stem with the dorsal ray. The cervical groove was absent. The anterior extremity was equipped with 20-22 external corona radiata, 4 cephalic papillae and 2 lateral amphids around the mouth. The eggs were 66.0×38.9 µm in average size. By the present study, B. diducta (Nematoda: Chabertiidae) is recorded for the first time in South Korea. Additionally, morphological characteristics and identification keys provided in the present study will be helpful in the faunistic or taxonomic studies for strongylid nematodes related.     

Aspects on the Ultrastructure of the Cephalic Region in Two Species of Acrobelinae (Nematoda,Cephalobidae)

The lip structures termed labial probolae, characteristic for the subfamily Acrobelinae, and the anterior sense organs have been studied by electron microscopy. The labial probolae consist of an amorphous tissue with denser strengthenings. They do not contain any sensory structures or musculature. The anterior sense organs consists of: (1) six inner labial sensilla, each with one receptor ending in a pore on a papilla; (2) six outer labial sensilla, each with one receptor ending in the cuticle; (3) four cephalic sensilla, each with two receptors, one ending in a pore on a papilla and the other in the cuticle; (4) two amphids, each with 12 sensory neurons basally; (5) accessory sensilla ventro-laterally. The combination of several chemoreceptive anterior sensilla and the morphological diversity of the labial probolae within the subfamily may aid in the utilization of different soil microhabitats.     

Morphological characterization of the antennal sensilla of t he earwig Anisolabis maritima (Dermaptera: Carcinophoridae) with reference to their probable functions

The earwig, Anisolabis maritima (Dermaptera: Carcinophoridae), is one of the most significant insects in KSA because, it was recorded in Saudi Arabia as a beneficial predator on eggs and newly hatched larvae of the red palm weevil, Rhyncophorus ferrugineus. We examined the external morphology of the antennal sensilla of males and females of A. maritima using scanning electron microscopy (SEM). The filiform antennae of A. maritima were of the conventional type comprising a basal scape, pedicle and a long, thread-like flagellum, which was composed of 12 flagellomeres of males and 16 flagellomeres of females. Six morphologically unique sensillar types were found and described on the antennae of males and females of A. maritima. Of those identified, there were three types of porous trichoid sensilla (long, curved and arcuate), and two types of basiconic sensilla (short and curved), and one type of aporous trichoid sensilla. The shape, external morphology and array of sensilla on the antennae of males and females of A. maritima were similar.     

Osteology,myology and feeding mechanism of Astronotus ocellatus (Pisces,Perciformes)

Summary Astronotus ocellatus captures its prey by creating a negative pressure in the buccal cavity which is caused by its quick expansion. Once the prey has been accommodated, the buccal cavity undergoes a compression which may propel the prey towards the pharyngeal jaws for mastication. The motion picture recordings indicate retracted premaxillae at the beginning of food intake followed by a maximum attainment of mouth gape and then mastication. During the maximum opening of the mouth the premaxillae are protruded and dentaries are at maximum depression. These events are followed by activities such as buccopharyngeal cavity expansion, bulging on the ventral surface of the head, and prominent curvature on the ventral surface anterior to the urohyal, caused by the upward movement of the glossohyal. Based on the cinematographic results, it may be inferred that the maximum mouth gape is caused by the sternohyoid-hyoid-interopercular-mandible coupling, and not by the opercular apparatus-mandible coupling, as the latter acts after the full descent of the lower jaw. Impression of the expanded buccopharyngeal cavity has been made by a paraffin mold technique, which confirms the displacement of the buccopharyngeal elements during expansion of the cavity.     

Scanning Electron Microscope Studies of Steinernema anomali Kozodoi, 1984

This paper presents SEM micrographs of portions of the male, female, and infective-stage juvenile of Steinernema anomali. Included are micrographs of the cephalic and caudal region, spicules, and gubernaculum of the male, the cephalic and vulval region of the female, and the cephalic region of the infective-stage juvenile. Males have six labial and four prominent cephalic papillae and small amphids. There are 11-14 pairs and one single genital papillae; of these, 6-9 pairs are preanal and subventral, one pair preanal, lateral, one pair adanal, and three pairs postanal. Spicules have a short head, a long blade, and a reduced shaft. The distal end is enlarged and bears a dorsal aperture. Gubernaculum much shorter than spicules; cuneus of gubernaculum short and bifurcate anteriorly. Females have six labial and four cephalic papillae and small amphids. Vulva with a thickened posterior lip. Infective juveniles have a smooth head, prominent amphids, and four cephalic papillae. Labial papillae, if present, are not evident.     

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.     

Drilomermis leioderma n. gen., n. sp. (Mermithidae:Nematoda) parasitizing Cybister fimbriolatus (Say) (Dystiscidae-Coleoptera)

The nematode Drilomermis leioderma n. gen., n. sp. (Merrnithidae) is described from larvae of Cybister fimbriolatus (Say) (Dytiscidae: Coleoptera) in Louisiana. Diagnostic characters of the genus Drilomermis are: medium-sized nematodes with the cuticle appearing smooth (lacking cross fibers) under the light microscope, six cephalic papillae, without mouth papillae, six hypodermal cords at midbody, 2 extremely long spicules (longer than 10 times body width at anus) which are separate and parallel (not twisted), an S-shaped vagina, medium-sized amphids located near head papillae, and postparasitic juvenile with a tail appendage. D. leioderma possesses a ventrally displaced mouth, very long vagina, and male genital papillae arranged in 3 double rows in the vicinity of the cloacal opening. Even when containing multiple parasites, about 40% of the hosts sulwived emergence of the memithids and lived several more days. In nature, some of these hosts may be able to continue their development, which is unusual since most mermithid-parasitized hosts die soon after the nematode emerges.     

Adhesion of Conidia of Drechmeria coniospora to Caenorhabditis elegans Wild Type and Mutants

Adhesion of conidia of the endoparasitic fungus Drechmeria coniospora to the cuticles of the wild type and four different head defective mutants of Caenorhabditis elegans, and subsequent infection, was studied. The conidia adhered around the sensory structures in the head region, vulva, and occasionally to other parts of the cuticle in both mutant and wild type hosts. Infection took place after adhesion to the head region by penetration through the cuticle, and, following adhesion around the vulva, through the natural orifice. Infection was not observed after adhesion to other parts of the cuticle. Adhesion was reduced after treatment of the nematodes with Pronase E. Adhesion returned towards normal again within 2 hours, indicating that the proteinaceous material emanating from the sensory structures was rapidly replaced.     

Fluorescent and Ferritin Labelling of Cuticle Surface Carbohydrates of Caenorhabditis elegans and Panagrellus redivivus

Caenorhabditis elegans and Panagrellus redivivus were investigated for surface carbohydrates using fluorescent-labelled and ferritin-labelled lectins. Rhodamine-labelled Concanavalin A was specifically located in the cephalic region of both species. Rhodamine-labelled wheat germ agglutinin was located over the entire cuticle of P. redivivus but was absent on C. elegans. Rhodamine-labelled peanut agglutinin and Limax flavus agglutinin did not label nematodes of either species. Galactose and sialic acid were not detected on either species, whereas mannose-glucose residues were specifically localized in the head areas of both species. No detectable N-acetylglucosamine occurred on C. elegans, but it was evenly distributed over the cuticle surface of P. redivivus.