Phonochorion Uvarov (Orthoptera: Tettigoniidae: Phaneropterinae) is a little known genus consisting of three species: Ph. satunini, Ph. artvinensis and Ph. uvarovi. The objective of this study is to conduct a thorough distributional, taxonomic and systematic revision of the genus Phonochorion using both bioacustic and external morphological characters. Field surveys indicate that the genus is distributed from the Trabzon region of Turkey to the Khulo province of Georgia however the exact limit of the eastern distribution of the genus remains unknown. Phonochorion species occur only on the northern slopes of the East Black Sea and Lesser Caucasus Mountains. The Coruh Valley, which seprates the East Black Sea and Lesser Caucasus Mountain ranges, seems to be an effective physical and climatic barrier and determines the distribution of these species. Ph. uvarovi can clearly be distinguished from Ph. satunini and Ph. artvinensis by the calling songs of males and external morphological characters. Ph. artvinensis and Ph. satunini differ in several taxonomic characters but the males have virtually identical calling songs. From a character evolution perspective, although geographically more distant, Ph. satunini is more closely related to Ph. uvarovi than Ph. artvinensis. Morphological similarities in several characters indicate Phonochorion to be most closely related to Polysarcus zacharovi and the Poecilimon heroicus-group. Within the genus Phonochorion, song structure and morphological characters clearly indicate Ph. uvarovi to be the basal taxon.
Gangesia parasiluri Yamaguti, 1934 (Cestoda: Proteocephalidae) is redescribed on the basis of adults obtained from the intestine of Silurus asotus Linnaeus (Teleostei: Siluridae) from Lake Suwa, Nagano Prefecture, central Japan. Its life cycle was studied in the field and laboratory. Rostellar hooks of the adults showed a wide variation in number, ranging from 35 to up to 57. Plerocercoids were found in the rectum of Chaenogobius urotaenia (Hilgendorf) and Rhinogobius brunneus (Temminck et Schlegel) (Teleostei: Gobiidae) from the same lake. Procercoids were formed in the haemocoel of Mesocyclops leuckarti (Claus) (Copepoda: Cyclopidae) 7 days post infection at 21-25°C. They developed into plerocercoids in the intestine of Pseudorasbora puntila pumila Miyadi (Teleostei: Cyprinidae), R. brunneus and S. asotus. Plerocercoids from naturally and experimentally infected fishes were fed to S. asotus, from which immature worms were recovered. It is considered that the life cycle involves three hosts: a copepod as the intermediate host in which procercoids are formed, small fish as paratenic hosts which retain plerocercoids and transport them into S. asotus, and S. asotus as the definitive host in which adults develop. Rostellar hooks of the adults were much fewer, much larger and arranged in fewer circles than those of the plerocercoids. It is suggested that the former are newly formed and replace the latter in an early stage of development of plerocercoids into adults in 5. asotus.
Soricinia tripartita Żarnowski, 1955 is redescribed on the basis of specimens from the type host Sorex araneus Linnaeus from Lithuania, Latvia and Russia (Republic of Karelia and Republic of Komi - a new geographical record) as well as from Sorex satunini Ognev and Sorex volnuchini Ognev from Russia (Nalchik Area in the Caucasus Mountains). The strobilar morphology of S. tripartita is compared with that of other hymenolepidid cestodes of shrews with an unarmed scolex and serial development of proglottides in the strobila, i.e. species of Mathevolepis Spassky, 1948, Ditestolepis Soltys, 1952, Spasskylepis Schaldybin, 1964, Ecrinolepis Spassky et Karpenko, 1983 and Diorchilepis Lykova, Gulyaev, Melnikova et Karpenko, 2006. It was noted that S. tripartita does not correspond to any of the known genera. The following unique characters are found for S. tripartita: heteronomous serial strobilation with one or two sterile proglottides at the end of each series in the strobila and the whole copulatory part of the vagina covered with numerous, fine spines. Therefore, the new genus Gulyaevilepis is erected, with Gulyaevilepis tripartita (Żarnowski, 1955) comb. n. as its type and only species. Since the type material of Soricinia tripartita is not known to exist, a neotype from the same host species and from a locality close to the type locality is designated.
Cystacanths of Corynosoma pseudohamanni Zdzitowiecki, 1984 (Palaeacanthocephala: Polymorphidae) are redescribed on the basis of specimens recovered from three species of Antarctic notothenioid fish, Trematomus bernacchii Boulenger, Gobionotothen gibberifrons (Lönnberg) and Notothenia coriiceps Richardson, collected from the Prince Gustav Channel, Antarctica. The cystacanths' morphometry and their internal anatomy including trunk muscles were studied using light and scanning electron microscopy (SEM). The characteristic features of this species such as the length of proboscis and the number of hooks (i.e. 260 hooks arranged in 20 rows with 13 hooks each, including two basal hooks) were confirmed and the intraspecific variability was evaluated. Sexual dimorphism was manifested in the shape of the hindtrunk, and the distribution and extent of the somatic armature only. SEM observations of internal anatomy revealed the detailed organization of trunk musculature.
Dracunculus globocephalus Mackin, 1927 (Nematoda: Dracunculoidea) is redescribed from specimens collected from the mesentery of the snapping turtle, Chelydra serpentina (L.), in Louisiana, USA. The use of scanning electron microscopy, applied for the first time in this species, made it possible to study details in the structure of the cephalic end and the arrangement of male caudal papillae that are difficult to observe under the light microscope. This species markedly differs from all other species of Dracunculus in having the spicules greatly unequal in size and shape, in the absence of a gubernaculum, and in the disposition of male caudal papillae. The validity of D. globocephalus is confirmed, but the above mentioned morphological differences are not sufficient for listing it in a separate genus. This is the first record of D. globocephalus in Louisiana.
Eimeria dorcadis Mantovani, 1966 is redescribed from dorcas gazelle (Gazella dorcas (L.)) from Saudi Arabia. Oocysts were detected in 7 out of 22 faecal samples (32%) using floatation method. The sporulated oocysts are cylindrical, slightly flattened at the micropylar pole, measure in average 32 × 19 μm (27-36 × 16-24 μm), length/width ratio being 1.7 (1.5-2.1). Oocyst wall is 1.2 μm thick, smooth, double-layered; outer layer is slightly thicker, light blue in colour; inner layer brownish, with micropyle in the inner layer and apparently continual outer one, measures 2.2 μm, but lacks a micropylar cap. The sporocyst elongate-ellipsoidal, measures 14 × 8 μm (12-17 × 6-9 μm), length/width ratio being 1.8, with sporocyst residuum as circular compact, coarse, refractile granules. Stieda body is present, while substieda body is absent. Sporozoites banana-shaped, measure 11 × 2.5 μm, each with a large spheroidal refractile body at the wider pole. Sporulation time is 2-3 days at 25 ± 2 °C.
Two fish cestodes, the little-known Eubothrium fragile (Rudolphi, 1802) and E. rugosum (Batsch, 1786), the type species of the genus Eubothrium Nybelin, 1922, are redescribed on the basis of new material from twaite shad, Alosa fallax (Lacépède, 1803), from England and burbot, Lota lota (Linnaeus, 1758), from Russia, respectively. The tapeworms are compared with two other species of the genus, E. crassum (Bloch, 1779) and E. salvelini (Schrank, 1790), common parasites of salmonid fish in the Holarctic. The most notable differential characters are the size and the shape of the scolex (smaller and oval in E. fragile), the shape of the apical disc (four or more indentations in E. crassum), the number and size of the testes (the largest and least numerous in E. rugosum), and the position and size of the vitelline follicles (almost entirely cortical in distribution in E. fragile and E. crassum versus largely medullary in E. rugosum and E. salvelini). A comparison of species has also shown the morphological similarity of the freshwater species (E. rugosum and E. salvelini) on one hand and those of marine origin, E. fragile and E. crassum, on the other, with the latter species occurring also in fresh waters. A key to the identification of the species studied is also provided.
The cystidicolid nematode Metabronema magnum (Taylor, 1925) is redescribed from specimens collected from the swimbladder of the fish (golden trevally) Gnathanodon speciosus (Forsskål) (Carangidae, Perciformes) off New Caledonia, South Pacific (a new geographical record). The light and scanning electron microscopical examination made it possible to study in detail the morphology of this so far little-known species. Its pseudolabia were found to possess distinct anterior protrusions (protuberances), sublabia are absent, only four cephalic papillae are present, deirids are bifurcated, and the male possesses six pairs of postanal papillae. By its morphology, M. magnum seems to be most similar to species of Salvelinema Trofimenko, 1962, also from the swimbladder of fishes, differing from them mainly in the presence of median wedge-shaped outgrowths in the mouth, lateral alae, the longer spicule on the right side, and a fewer number of pairs of preanal papillae in the male. Since the morphology of M. magnum considerably differs from that of other representatives of the Cystidicolidae, Metabronema in Rasheed's (1966) conception is considered a valid genus.
Pterygodermatites (Mesopectines) nycticebi (Mönnig, 1920) (Nematoda: Spirurida: Rictulariidae) is redescribed based on immature and mature adults collected from the stomach and small intestine at autopsy of a slow loris, Nycticebus coucang (Boddaert, 1785) (Mammalia: Primates), in a zoological garden in Japan. It is first demonstrated that male possesses a minute telamon and a left lateral pore in the preanal part of body. The cause of death of the slow loris is strongly surmised to be related to the nematode infection, which was apparently acquired under captivity in the zoological garden.
A redescription of the female of the temporary fish parasite, Gnathia africana Barnard, 1914 is provided from specimens reared from final-stage G. africana praniza larvae collected from their intertidal fish hosts along the south coast of southern Africa. It differs from other known gnathiid females in the shape of the frontal border and the number and basic form of pylopod articles. This redescription aims to establish a format for future descriptions and redescriptions of gnathiid females.