In the apical glandular region of the adult Proteocephalus torulosus (Batsch, 1786), two types of eccrine gland cells are present. The first type of unicellular gland produces large electron-dense granules of various sizes. The second type contains small electron-dense granules. Most cells form glands with large granules; glands with small granules are infrequent. The secretion of both types of gland cells is concentrated in the apical parts of the cyton and in the ducts opening to the exterior. On the scolex of P. torulosus, there are regional structural differences of the microthrix border. The apical glandular region bears filamentous microtriches only. On the remaining frontal part, surrounding the glandular region, there are blade-like and filamentous microtriches. The lateral parts of the scolex and suckers bear blade-like microtriches. Possible functions of both types of gland cells and different parts of the scolex microthrix border are discussed. The unique structure of the frontal part of the scolex of P. torulosus and its differences from Proteocephalus macrocephalus, P. longicollis and P. percae correlate well with the putative basal phylogenetic position of P. torulosus among European species of Proteocephalus.
The ‘buccal complex’ of Pricea multae Chauhan, 1945 consists of two buccal suckers, the pharynx, a putative taste organ and the mouth cavity. The two suckers are dorsal to the mouth cavity, and the pharynx posterior to them. The septum in each sucker consists of connective tissue containing muscle filaments, lined by tegument with short irregular microvilli. The mouth cavity and the lumen of the suckers are lined by tegument with short irregular lamellae and by tegument with long bulbous, interconnected lamellae, separated from each other and from the body surface tegument by septate junctions. A ventral extension of the mouth cavity is also lined by tegument with short irregular lamellae. An anterior ‘taste organ’ is lined by ‘normal’ (body) tegument and tegument with short irregular lamellae. Glandular ducts open into it, and it contains many small uni-ciliate and multiciliate receptors, as well as two receptor complexes each consisting of a large non-ciliate receptor surrounded by small and large uniciliate receptors, with multiciliate receptors closeby. The four types of receptors are described in detail. The anterior part of the pharyngeal lumen is lined by an epithelium with dense surface lamellae and is penetrated by non-ciliate receptors. Attention is drawn to significant differences between the buccal complexes of the polyopisthocotylean monogeneans Pricea multae (Gastrocotylidae), Gotocotyla secunda (Tripartii, 1956) (Gastrocotylidae), Pulylabroides australis (Murray, 1931) (Microcotylidae), Zeuxapia serialae (Meserve, 1938) (Axinidae) and Diclidophora merlangi (Kuhn, 1832) (Diclidophoridae).
The forebody and foregut of Crepidostomum metoecus Braun, 1900 are invested with a tegument bearing regularly arranged surface tubercles comparable with the aspidogastrean surface structures. The tegument of the ventrolateral lobes and of the prepharynx is penetrated by ducts of eccrine gland cells. The frontal and prepharyngeal gland cells, localised in the parenchyma, discharge electron-dense granules. Their ducts are lined by peripheral microtubules and fixed to the tegument plasmalemma by a septate junction. The functional roles of these glands are discussed.
While the majority of polyopisthocotylean monogeneans feed on blood, some polystomatids infecting chelonians do not. This study examined the gastrodermis of two polystomatids, one - Neopolystoma spratti Pichelin, 1995 - from the conjunctival sac of a chelonian and the other - Concinnocotyla australensis (Reichenbach-Klinke, 1966) - from the oral cavity, gill arches and primary gill lamellae of a fish, and also found no evidence of blood feeding. However, the gastrodermal architecture in both species basically resembles that found in blood feeding polyopisthocotyleans, with alternation of lamellated digestive cells and an intervening syncytium. In C. australensis, oesophageal secretion appeared to be responsible for initial extracellular digestion and this was followed by pinocytotic uptake of partly degraded material in pits between the numerous apical lamellae of digestive cells. Posterior dorsolateral gut pockets unique to C. australensis were shown to be blind sacs separated from the external environment by a narrow cytoplasmic bridge, composed of a thin layer of tegument apposed to a thin layer of pocket syncytial epithelium. The pockets are lined with greatly folded syncytium and set in a “capsule” of tissue in which numerous pro-tonephridial flame cells are embedded. It is suggested that the pockets have an osmoregulatory function related to the particular environment and evolutionary history of the host, the primitive lung fish (Dipnoi) Neoceratodus forsteri (Krefft, 1870).
An ultrastructural study of the ovarian follicles and their associated oviducts of the cestode Gyrocotyle urna Grube et Wagener, 1852, a parasite from the spiral valve of the rabbit fish, Chimaera monstrosa L., was undertaken. Each follicle gives rise to follicular oviduct, which opens into one of the five collecting ducts, through which pass mature oocytes. These collecting ducts open into an ovarian receptacle which, in turn, opens via a muscular sphincter (the oocapt) to the main oviduct. The maturation of oocytes surrounded by the syncytial interstitial cells within the ovarian follicles of G. urna follows a pattern similar to that in Eucestoda. The ooplasm of mature oocytes contain lipid droplets (2.0 × 1.8 µm) and cortical granules (0.26 × 0.19 µm). The cytoplasm of primary and secondary oocytes contains centrioles, indicating the presence of the so-called ''centriole cycle'' during oocyte divisions. A morphological variation between different oviducts was observed. The luminal surface of the follicular and the collecting oviducts is smooth. The zones of the septate junctions are present within the distal portion of the net-like epithelial wall of the collecting ducts close to the ovarian receptacle. The syncytial epithelial lining of the ovarian receptacle, oocapt and main oviduct is covered with lamellae and cilia. Cortical granules secreted from mature oocytes occur freely within the lumen of the main oviduct that functions as a fertilisation canal. A division of the ovary into separated parts with their own collecting ducts as that typical of Gyrocotyle has been observed in neodermates, basal monogenean family Chimaericolidae, and Neoophora (some Proseriata and Fecampiidae). Ultrastructural data thus reveal several unique morphological characteristics of gyrocotylideans, the most basal taxon of tapeworms (Cestoda).
Ultrastructure of the primitive epithelium of Echinostoma revolutum (Digenea: Echinostomatidae) cercaria was studied. The germinal balls and developing cercariae are covered with the primitive epithelium in daughter rediae. When the definitive tegument of the cercaria is differentiated, the primitive epithelium degenerates. The last remnants of the primitive epithelium in a cercaria can be detected at the stage when the lateral gland cells have released their secretion into the definitive tegument.
The ultrastructure of the scolex tegument, bothridial pits (“ciliated pits) and rhyncheal system of Otobothrium mugilis Hiscock, 1954 is described from plerocerci collected from the teleosts Arius graeffei Kncr ct Steindachner and Mugil cephalus Linnaeus. Scanning electron microscopy revealed that filamentous microtriches with shortened caps are abundant across the entire surface of the tegument. Palmate microtriches are dominant on the bothridia and their margins. The surfaces of bothridial pits were covered with large bifid microtrichcs. The bothridial pits arc strongly muscularised invaginations of the tegument. Nervous tissues were not observed within the pits and it is probable that these structures function as accessory attachment structures. The wall of each tentacle sheath consists of one to three bands of fibrils, lined internally by a thin cytoplasmic layer. The tentacular walls are cellular, containing myofilaments. The fibrils of the tentacular walls are arranged into discrete blocks of parallel fibrils and appear to be intracellular. Tentacular walls are lined externally by a modified membrane with an external glycocalyx. Tentacular hooks arc solid, bound externally by a membrane. The body of the hook contains numerous longitudinal canaliculi and an elcctron-opaquc medulla lies at the centre of the hook.
The secondary osmoregulatory canals in the scolex and neck region of Silurotaenia siluri, a parasite of the catfish Silurus glanis (L.), terminate below the tegument basal plasma membrane. The basal plasma membrane of the osmoregulatory canal syncytium is in tight contact with the tegument basal plasma membrane.
The present study describes the ultrastructure of the mature spermatozoon of Lecithocladium excisum (Rudolphi, 1819) (Digenea: Hemiuroidea: Hemiuridae) from the stomach of the marine teleost Scomber japonicus Houttuyn (Scombridae) captured in the Atlantic Ocean, off Dakar (Senegal). The ultrastructural organization of the spermatozoon of L. excisum follows the general model described in most digeneans. It presents two axonemes of the 9+'1' pattern of the Trepaxonemata, nucleus, mitochondrion and parallel cortical microtubules, among other characters. However, some particularities of the spermatozoon of L. excisum are (i) the presence of a membranous ornamentation not associated with cortical microtubules in its anterior extremity, (ii) the presence of a very reduced number of cortical microtubules located only in the ventral side of the spermatozoon and (iii) the absence of several structures described in most digeneans such as spine-like bodies and cytoplasmic expansions.
The surface structures and gland cells of the posterior rosette organ of Gyrocotyle urna Grube et Wagener, 1852, a member of the group presumed to be the most basal of the tapeworms (Cestoda: Gyrocotylidea), was studied by scanning electron and transmission electron microscopy. Surface structures on the outer (oriented away from the intestinal wall) and inner (in contact with the intestinal wall) rosette surfaces differ from each other and represent a transitional form between microvilli and microtriches typical of tapeworms (Eucestoda). The inner surface of the rosette possesses numerous glands. On the basis of the size and electron-density of their secretory granules, three types of unicellular gland cells can be distinguished. The least common type (Type I) is characterized by the production of small, round, electron-dense granules of about 0.3 µm in diameter, whereas another type of secretion (Type II) is formed from homogenous, moderately electron-dense, spheroidal granules of about 0.7 µm in diameter. The most common type of glands (Type III) is recognized by a secretion comprising large, elongate, electron-dense granules of about 1 µm long and 0.5 µm broad. The secretory granules of the three types of the glands are liberated by an eccrine mechanism and the gland ducts open via small pores on the inner rosette surface. The complex of secretory glands of the posterior rosette of G. urna is similar to those in the anterior attachment glands of monogeneans (as opposed to the types of glands present in other helminth groups). However, the tegumental surface structures of Gyrocotyle are supporting evidence for the relationship between the Gyrocotylidea and Eucestoda.