The development of the swimbladder nematode Anguillicola crassus Kuwahara, Niimi et Itagaki, 1974 in the definitive host (eels) was studied under experimental conditions. Small eels, Anguilla anguilla (L.) with body length 8-16 cm were infected by feeding them intermediate host copepods (Cyclops strenuus Fischer) harbouring third-stage larvae of this parasite. These experiments showed that, at 20-22° C, the development from the third-to the fourth-stage larvae lasted approximately three weeks, but some retarding third-stage larvae occurred in the wall of the host’s swimbladder or hyperparasitizing in the cuticle of adult nematodes as late as three months p.i. Young adults developed in the lumen of the swimbladder within approximately one month and noneinbryonated eggs first appeared in females 6-7 weeks p.i. The prepatent period was about three months and the patent period could be estimated to last no more than a month. Females degenerated soon after oviposition. The experiments confirmed that the size of mature A. crassus depends on the body size of its definitive host (eel).
The development of the nematode Syncuaria squamata (Linstow, 1883), a gizzard parasite of cormorants, was experimentally studied in the ostracod Notodromas monacha. After the eggs of this nematode have been swallowed by the ostracod, the toothed first-stage larvae of the parasite are released and penetrate through the intestinal wall into the haemocoel of the crustacean. Before attaining the infective third stage, the larvae moult twice in the body of the intermediate host (9-11 and 13-15 days after infection at water temperatures of 20-22° C). The fishes Alhumaides hipunctatus, Noemacheilus barbatulus, Oncor-hynchus mykiss and Poecilia reticulata were for the first time recorded as suitable experimental paratenic hosts of S. squamata third-stage larvae in which a slight growth of larvae may occur. The first recorded natural paratenic host of this nematode was tench, Tinca tinea, originating from a South-Bohemian pond where cormorants occur. Paratenic hosts are apparently the main source of S. squamata infection for cormorants.
An examination of a sample of European eels, Anguilla anguilla (L.), collected from Lake Bracciano near Rome in 1993, the only known European locality with the occurrence of the introduced swimbladder nematode Anguillicola novaezelandiae Moravec et Taraschewski, 1988, revealed for the first time the presence of two Anguillicola species, A. novaezelandiae and A. crassus. In view of the investigations carried out by current authors in Bracciano Lake in the years 1982-1992, it is apparent that the latter species has been introduced into the lake quite recently, where it quickly became a dominant species. The development of A. novaezelandiae was experimentally studied in the copepod intermediate host, Cyclops strenuus, for the first time. The copepods were infected with nematode second-stage larvae at 21-22°C; fully developed infective third-stage larvae were obtained 13 days p.i. The general morphology of individual larval stages of A. novaezelandiae was similar to that of larvae of the related species Λ. crassus.
Three species of planktonie crustaceans, Cyclops strenuus and Macrocyclops alhidus (Copcpoda) and Notodromas monacha (Ostracoda), were experimentally infected with the eggs and second-stage larvae of the swimbladder nematode Anguillicola crassus originating from eels from Neusiedler Lake in Austria. At 20-22°C, third-stage larvae of the parasite developed in all these invertebrate hosts within 16-20 days p.i. Ostracods harbouring the nematode third-stage larvae (33 days p.i.) were fed to small eels (Anguilla anguilla), while infected copepods (20 days p.i.) to seven other fish species. By these experiments, the larvae from ostracods proved to be infective for the definitive host and the ostracod was thus confirmed as a true intermediate host of Anguillicola crassus. Notodromas monacha represents a new experimental intermediate host of A. crassus and the second known invertebrate other than a copepod in which the larval development of this nematode up to the infective stage takes place. Five species of fish, cyprinids Tinca tinea, Alhumus alburnus, Gobio gobio and Albumoides bipunctatus (the latter representing a new host record), and guppy, Poecilia reticulata, were found to serve as experimental paratenic hosts for A. crassus, in which the live nematode infective larvae were recorded 49 days p.i.
The development of the nematode Anguillicola crassus, a swimbladder parasite of eels, was experimentally studied in copepod intermediate hosts Cyclops strenuus and Acanthocyclops vernalis. The copepods, kept at a laboratory temperature of 20-22 °C, were infected with nematode second-stage larvae; the second moult of larvae (the only one in the intermediate host) was observed to start 10 days p,i„ but third-stage larvae liberated from their cuticular sheath were first observed 20 days p.i. These proved to be infective for experimental eels. Free second-stage larvae as well as larvae from copepods were described. The morphology of A. crassus larvae and the mode of their development in the intermediate host were compared with those of other dracunculoid nematodes. From this point of view, Anguillicola members appear to represent an ancient group of dracunculoid nematodes.
A description is given of the life cycle of the nematode Procamallanus (Spirocamallanus) rebecae (Andrade-Salas, Pineda-Lopez et García-Magafia, 1994), an intestinal parasite of cichlids in Mexico. The copepod Mesocyclnps sp. was found to be a suitable experimental intermediate host. After the copepod’s ingestion of free first-stage larvae of the nematode, these enter the haemocoel of the intermediate host; they moult twice (on the 3rd and 5-6th day p.i. at 21-22”C) before they attain the third, infective stage. The third-stage larva already possesses the large buccal capsule without spiral thickenings and its tail tip bears three cuticular spines. The larvae undergo two additional moults (13-14 days and 42 days p.i.) in the definitive host (Cichlasoma urophthalmus) before changing to adults; the prepatent period is about 2-3 months. Experimental infection of guppies, Poecilia reticulata, have shown that these fishes may become paratenic (metaparatenic) hosts of this parasite. The morphology of individual larval stages of this nematode is described.