Based on light and scanning electron microscopical studies, eight species (five adult and three larval) of nematodes belonging to the Ascaridida, Oxyurida and Enoplida were collected from fishes of the Okavango River, Botswana, namely Falcaustra similis Moravec et Van As, 2004, Atractidae gen. sp. (only female) (both Cosmocercoidea), Cucullanus sp. (only female) (Seuratoidea), Cithariniella longicaudata sp. n., Synodontisia annulata sp. n. (both Oxyuroidea), Contracaecum sp. third-stage larvae, third-stage larvae of Galeiceps sp. (both Ascaridoidea) and Eustrongylides sp. fourth-stage larvae (Dioctophymatoidea). The new species Citharinella longicaudata (type host Schilbe intermedius Rüppel) is mainly characterised by the shape and size of cephalic papillae and the spicule 108 µm long, and Synodontisia annulata (type host S. intermedius) by the shape of cephalic papillae, body length of gravid females (4.88-5.33 mm) and a short spicule (66 µm long). The female specimen of Cucullanus sp. from Tilapia sparmanni Smith markedly differs from congeners parasitising inland fishes in Africa by the elongate pseudobuccal capsule and by the excretory pore far posterior to the oesophago-intestinal junction; apparently, it belongs to an undescribed species. Galeiceps larvae parasitising fishes are described for the first time. This paper is a continuation of these studies, based on the same nematode collection, now providing results of the systematic evaluation of nematodes of the orders Ascaridida, Oxyurida and Enoplida. Detailed morphological examinations (using both light and scanning electron microscopy) of these materials revealed the presence of several species, including three new taxa of adults and previously undescribed larvae of a little-known anisakid genus. The results are presented herein.
MATERIALS AND METHODSA total of 169 specimens belonging to nine fish species of the families Alestidae, Cichlidae, Clariidae, Mochokidae and Schilbeidae were collected in the Okavango River (mainstream in the Shakawe area) in the Panhandle, by gill nets, cast-nets and electro-fishing. Fish were taken live to a nearby field laboratory and maintained unfed in plastic tanks for at least two days to allow the gut to empty. The fish were anaesthetised and killed using MS222 and the internal organs were removed and placed in 1% saline. Nematodes removed from the digestive tract and viscera were fixed in 4% or 10% buffered neutral formalin.For light microscopical examination, the nematodes were cleared gradually in glycerine. Drawings were made with the aid of a Zeiss microscope drawing attachment. Specimens used for scanning electron microscopy (SEM) were post-fixed in 1% osmium tetroxide (in phosphate buffer), dehydrated through a graded ethanol series, critical-point-dried and sputter-coated with gold; they were examined using a JEOL JSM-7401F scanning electron microscope at an accelerating voltage of 4 kV (GB low mode). All measurements are in micrometres unless otherwise indicated. Only small numbers of the available s...