ABSTRACT
A new species of parasitic nematode, Procamallanus (Procamallanus) pacificus n. sp., is described from the stomach of the Pacific shortfinned eel, Anguilla obscura (type host), and from the speckled longfin eel, Anguilla reinhardtii, from northern New Caledonia (Melanesia, South Pacific); from Anguilla sp. (cf. obscura) from the Fiji Islands (Melanesia, South Pacific); and from the giant mottled eel Anguilla marmorata from Futuna Island (Wallis and Futuna Islands, Polynesia). Although a total of 450 nematodes were collected, all specimens were females; this suggests either an extremely rare occurrence of males or parthenogenetic reproduction in this species. Procamallanus pacificus differs markedly from all congeners from fish hosts in possessing a greater number (4-9) of caudal mucrons in the female and by other morphological features. This parasite might become a serious pathogen of cultured eels in the region of the South Pacific. Batrachocamallanus Jackson and Tinsley, 1995 is considered a junior synonym of Procamallanus Baylis, 1923, to which 2 species are transferred as Procamallanus occidentalis (Jackson and Tinsley, 1995) n. comb. and Procamallanus siluranae (Jackson and Tinsley, 1995) n. comb. One third-stage larva of Procamallanus (Spirocamallanus) sp. was also recorded from Anguilla sp. (cf. obscura) from the Fiji Islands.
Subject(s)
Anguilla/parasitology , Fish Diseases/parasitology , Nematoda/classification , Secernentea Infections/veterinary , Animals , Female , Microscopy, Electron, Scanning/veterinary , Nematoda/ultrastructure , Secernentea Infections/parasitologyABSTRACT
A new species of parasitic nematode, Cucullanus oceaniensis sp. n., is described from the intestine of the giant mottled eel Anguilla marmorata (type host) from Futuna Island (Wallis and Futuna Islands, Polynesia) and from A. marmorata and Anguilla sp. (cf. obscura) from Fiji Islands (Melanesia, South Pacific). The main distinguishing characteristics are the length of spicules (668-1,020 microm), situation of deirids (slightly anterior to the oesophago-intestinal junction) and the excretory pore (some distance posterior to the end of oesophagus), and the arrangement of caudal papillae in the male. It is the third known species of Cucullanus from Oceania and the first one reported from freshwater eels in the region of South Pacific. Cucullanus faliexae Morand et Rigby, 1998 is considered a junior synonym of Cucullanus australiensis Baylis, 1927.
Subject(s)
Anguilla/parasitology , Fish Diseases/parasitology , Nematoda/anatomy & histology , Nematoda/classification , Nematode Infections/veterinary , Animals , Female , Fiji , Fresh Water , Male , Microscopy, Electron, Scanning/methods , Microscopy, Electron, Scanning/veterinary , Nematoda/isolation & purification , Nematoda/ultrastructure , Nematode Infections/parasitology , PolynesiaABSTRACT
The swimbladder of the adult eel, Anguilla anguilla, with its bipolar countercurrent system, the rete mirabile, is a widely used model for swimbladder function, but very little is known about the development of this swimbladder. Our histological studies on the developing swimbladder revealed that during metamorphosis the swimbladder becomes present as a dorsal outgrowth of the esophagus. It is filled with surfactant, and gas was not detected in the swimbladder. In the young glass-eel, the epithelial (gas gland) cells of the swimbladder are columnar, but do not yet have the typical basolateral labyrinth established in adult animals. Few blood vessels are found in the swimbladder tissue, and the submucosa is present as a thick layer of connective tissue, giving a large diffusion distance between blood vessel and swimbladder lumen. Within the next 2 or 3 months of development, gas gland cells develop their typical basolateral labyrinth, and the thickness of the submucosa is significantly reduced, resulting in a short diffusion distance between blood vessels and the swimbladder lumen. The first filling of the swimbladder with gas is observed while the gas gland cells are still in a poorly differentiated status and it appears unlikely that these cells can accomplish their typical role in gas deposition. The presence of small gas bubbles in the swimbladder as well as in the ductus pneumaticus at the time of initial swimbladder inflation suggests that the swimbladder is filled by air gulping or possibly by taking up gas bubbles from the water.