The posterior attachment organ (sucker) of Temnocephala sp. is located ventrally attached to the posterior end of the body by a well defined stalk; those of Udonella caligorum Johnston and Anoplodiscus cirrusspiralis Roubal, Armitage et Rohde are extensions of the posterior end facing posteriorly. In Philophthalmus, the sucker is ventrally embedded in the main body. The sucker of Temnocephala is lined by an epidermis, its ventral part separated from the adjacent epidermis by a septate junction. The epidermis resembles that of the body proper, containing nuclei and numerous dense bodies, its surface enlarged by short microvilli, traversed by glandular ducts of two types and by sensory receptors, and based on a basal lamina with a thick underlying fibrous matrix. The stalk of the sucker contains many muscle fibres extending from the main body into the sucker. The posterior surface of the sucker of Udonella is separated from the adjacent tegument by a septate junction; it consists of numerous microvilli arising from the basal lamina and does not represent a tegument; glandular ducts of two types open through it, and muscle fibres extend from the body proper into the sucker. The posterior surface of the sucker of Anoplodiscus consists of a thin tegument not separated from the adjacent tegument by a septate junction, drawn out into a very large number of densely packed, long microvilli, some branching from a thick cross-striated base; large glandular ducts open postero-laterally. The ventral sucker of Philophthalmus is embedded in the body proper but clearly bounded by a “capsule” of basal lamina; it is lined by a tegument continuous with that of the main body and lacking microvilli except in a small band around the ventral sucker opening. There is no evidence from ultrastructure that the stickers of the four taxa are homologous. Since there is no convincing other evidence for the homology of the posterior attachment organs of the major groups of parasitic Platyhelminthes (Neodermata) and the Temnocephalida, a “cercomer theory” assuming such homology cannot be accepted as proven.
The localisation and distribution of the serotoninergic nerve elements was studied for the first time in the flatworm Chimaericola leptogaster (Leuckart, 1830) using immunocytochemical methodology and confocal laser scanning microscopy. The musculature was investigated by histochemical staining of actin filaments; scanning electron microscopy was used to identify the sensory structures on the worm's surface. Uniciliated, bi-ciliated and multiciliated sensory endings have been described on the worm's surface. The morphological data demonstrate the presence of circular, longitudinal and diagonal muscles that comprise the musculature of C. leptogaster in the anterior, median and posterior body regions. Well-developed radial and circular muscle fibres were also observed surrounding the genital pore, two vaginae and in clumps of the haptor. The study revealed the presence of biogenic amine, serotonin, in the central and peripheral nervous systems of C. leptogaster: in the neurons and fibres of the cephalic ganglia and ventral nerve cord, in the innervation of reproductive system compartments. The localised sites of the serotoninergic elements point to important roles of serotonin in monogenean reproductive processes and, possibly, in the regulation of muscle function., Natalya V. Mochalova, Nadezhda B. Terenina, Larisa G. Poddubnaya, Valery A. Yashin, Andrei V. Kuchin, Natalya D. Kreshchenko., and Obsahuje bibliografii
The taxonomy of Diplectanum Diesing, 1858, a genus of monopisthocotylean monogeneans, remains unsettled and needs to be revised based on new morphological criteria. Recent studies in monopisthocotyleans have shown that the muscle arrangement in the posterior attachment organ (haptor) differs between congeneric species and can be used as an additional criterion in genus-level taxonomy. To explore the possibility of using the haptoral musculature and nervous system in the taxonomy of Diplectanum, we conducted a detailed confocal-microscopy study of three species of Diplectanum (D. aculeatum Parona et Perugia, 1889, D. sciaenae van Beneden et Hesse, 1863 and D. similis Bychowsky, 1957) with phalloidin staining for muscle and indirect immunostaining for 5HT and FMRFamide. A further goal was to clarify the functional mechanics of the haptor and the role of its essential components (squamodiscs and anchors) in attachment to the host. The system of connecting bars and gaffing anchors was found to have a complex musculature consisting of 23 muscles in D. aculeatum and D. sciaenae, and 21 muscles in D. similis. The squamodiscs were shown to be operated by several groups of muscles attached primarily to the area termed the squamodisc fulcrum. Most of the haptoral musculature is identical in D. aculeatum and D. sciaenae and these species differ only in the presence of a muscle sheath around the tissue strand between the squamodiscs in D. sciaenae and in the different patterns of superficial squamodisc muscles. Diplectanum similis shows more significant differences from the other two species: besides lacking two of the haptoral muscles, it also differs in the shapes and arrangement of several other muscles. The nervous system of all three species conforms to the general pattern typical for the Dactylogyroidea and shows little variation between species., Anatoly A. Petrov, Evgenija V. Dmitrieva, Maryana P. Popyuk, Pavel I. Gerasev, Sergey A. Petrov., and Obsahuje bibliografii