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.
The species Beludzhia phylloteliptera Rohdendorf is redescribed from adult males and females as well as all larval instars collected in the United Arab Emirates. The morphology of the first instar larva is strikingly similar to that of Dolichotachina marginella (Wiedemann) and Phylloteles pictipennis Loew, all of which are here documented for the first time. These three generic representatives share several character states, which are probably plesiomorphic relative to the condition observed in other miltogrammine larvae, but the uniquely shaped, slender mouthhook, a cushion- or pad-like lobe behind the maxillary palpus (cheek organ), the antero-ventral segmental prolegs of the first instar larva, and the integumental warts of the third instar larvae, are shared character states not known from any other species of Sarcophagidae. Beludzhia Rohdendorf is therefore placed with Dolichotachina Villeneuve and Phylloteles Loew in the tribe Phyllotelini.
A phylogenetic analysis of the four coleopteran suborders (Polyphaga, Archostemata, Myxophaga and Adephaga), four other endoneopteran taxa (Strepsiptera, Neuropterida, Mecopterida and Hymenoptera) and three neopteran outgroups (Orthoneoptera, Blattoneoptera and Hemineoptera) is performed based on 63 characters of hind wing venation, articulation and folding patterns, with character states coded for the groundplan of each taxon (not for exemplar genera or species). The shortest tree found using Winclada with Nona exhibits the following topology: Orthoneoptera + (Blattoneoptera + (Hemineoptera + Endoneoptera: (Hymenoptera + ((Neuropterida + Mecopterida) + (Coleoptera + Strepsiptera))))). Homologization of the hind wing venation in Coleoptera is reviewed and updated, and comments are made concerning recent works on wing folding. Recent phylogenetic schemes proposed for the orders of Endoneoptera and suborders of Coleoptera are reviewed and their supporting evidence critically examined. The special role and influence of the hind wing anojugal lobe on the diversification of Neoptera and Endoneoptera is discussed. A scenario is proposed for the origin and evolution of the insect hind wing.
This paper presents a synthesis of morphological information on larvae of the beetle suborder Archostemata. Larvae of the following families and species were studied: Ommatidae: Omma sp.; Micromalthidae: Micromalthus debilis LeConte, 1878; Cupedidae: Priacma serrata LeConte, 1861, Distocupes varians (Lea, 1902), Rhipsideigma raffrayi (Fairmaire, 1884), Tenomerga cinerea (Say, 1831) and Tenomerga mucida (Chevrolat, 1829). Morphological characters of the suborder and three families are described. Monophyly of the suborder is strongly supported by more than 10 larval autapomorphies. A close relationship between Micromalthidae and Cupedidae is confirmed. New larval characters are introduced, including chaetotaxy of first instar larvae of Micromalthus LeConte, 1878, Priacma LeConte, 1874 and Distocupes Neboiss, 1984. An identification key to families and subfamilies of Archostematan larvae is provided, along with a checklist of extant Archostemata taxa. The work is illustrated with 120 morphological drawings.