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.
The frontal gland as a sac-like organ in Prorhinotermes simplex is present only in presoldiers, soldiers, and imagoes, but exists also in nymph-soldier intercastes. The secretory epithelium consists of a single type of secretory cells adhering directly to the cuticular intima. Secretory vacuoles originate in electron dense vesicles, which are transformed into large electron lucent vacuoles. Intermediate vacuoles frequently contain lipid droplets. The frontal gland cells in presoldiers reveal modifications connected with the production of a new cuticle; the new cuticle is thin and compact, whereas the old one is thick, porous, and wrinkled. None of these cuticles is present in soldiers (sic!). In soldiers, the cuticular intima is of endocuticular origin and is formed by dispersed dense material; the apical parts of secretory cells are formed by numerous irregular finger-like projections, true microvilli are completely lacking. In imagoes, the cuticle is composed of an epicuticle, a layer of epicuticular filaments, and one more basal layer; sexual differences were not observed. In nymph-soldier intercastes, the structure of the gland differs in the head and in the metathorax; the head part of the gland resembles the imaginal gland whereas the thoracic part resembles more that of the soldier; the development of secretory vacuoles stops at the stage of presence of lipid droplets. E-1-nitropentadecene was found in the highest amount in soldiers (comparable to P. inopinatus soldiers), in moderate amount in imagoes, and it is missing in both presoldiers and intercastes.
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.
In the present paper, we describe the ultrastructure of the spermatozoon of the notocotylid Notocotylus noyeri (Joyeux, 1922) by means of transmission electron microscopy. The mature spermatozoon of N. noyeri exhibits the general pattern described in the majority of digeneans: two axonemes of the 9 + "1" pattern of the Trepaxonemata, nucleus, mitochondria, parallel cortical microtubules, spine-like bodies and ornamentation of the plasma membrane. The glycogenic nature of the electron-dense granules was evidenced applying the test of Thiéry. The ultrastructural features of the spermatozoon of N. noyeri present some differences in relation to those of the Pronocephalidea described until now, but confirm a general pattern for the Notocotylidae, namely a spermatozoon with two mitochondria and an anterior region with ornamentation of the plasma membrane associated with spine-like bodies. The posterior extremity of the spermatozoon exhibits only some microtubules after the disorganisation of the second axoneme. The present study confirms that some ultrastructural characters of the sperm cell such as the presence or absence of lateral expansions, the number of mitochondria and the morphology of both anterior and posterior spermatozoon extremities are useful for phylogenetic purposes within the Pronocephaloidea. Thus, unlike notocotylids, pronocephalids exhibit external ornamentation and a lateral expansion in the anterior spermatozoon region. Moreover, notocotylid spermatozoa present two mitochondria, whereas pronocephalid spermatozoa exhibit a single mitochondrion. Finally, pronocephalids are characterised by a type 2 posterior spermatozoon extremity, whereas notocotylids exhibit a type 3 posterior spermatozoon extremity., Papa Ibnou Ndiaye, Jordi Torres, Catarina Eira, Vladimir V. Shimalov, Jordi Miquel., and Obsahuje bibliografii