The claim by many authors that Spinitectus inermis (Zeder, 1800), a narrowly specific parasite of European eels Anguilla anguilla (L.), is a rare species is considered at three levels: its geographical range, its frequency of occurrence compared to other eel parasites and its relative abundance in component communities. The parasite is widely distributed in freshwater throughout the European range of the eel but its occurrence is erratic and unpredictable, being known from only 8 countries. Surveys of eel parasites in the United Kingdom and in Continental Europe show that it is present in only 13% of British and 29% of continental localities. This satisfies one of the criteria for rarity. When present, its prevalence ranges from 1.8% to 43.3%, so it can be considered rare in some localities but in a few it may be common and on occasion it may be the dominant species in the gastro-intestinal community. Populations of S. inermis are almost always characterised by high levels of overdispersion, even at low prevalence. The species also displays an ability to colonise a locality following introduction there. Overall it meets many of the criteria of a rare species including a restricted distribution and a low frequency of occurrence and so it can be considered to exhibit diffusive rarity.
The development of the nematode Spinitectus inermis (Zeder, 1800), a parasite of the stomach of eels, Anguilla anguilla (L.) in Europe, was experimentally studied. Mayfly nymphs Caenis macrura, Ecdyonurus dispar, Heptagenia sulphurea, Potamanthus luteus and Seratella ignita from Portugal and the Czech Republic were found to serve as experimental intermediate hosts. After ingestion of the nematode eggs by the mayfly nymphs, the toothed first-stage larvae were released and penetrated into the body cavity of the intermediate host. There they moulted twice (on day 4 and 6 post infection [p.i.] at water temperatures of 20-25°C), attaining the third infective stage. The definitive host, A. anguilla, undoubtedly acquires infection by feeding on mayfly nymphs harbouring infective-stage larvae. In an experimentally infected eel, the fourth-stage larva undergoing the third moult was observed 28 days p.i. at water temperature of 20ºC. The larval stages, including moulting forms, are described and illustrated. The prepatent period of S. inermis is estimated to be about two months.
Following the introduction of Anguillicola crassus into Lake Balaton, by 1991 the entire eel population became infected. At the same time, marked differences existed in the prevalence and intensity of infection between different areas of the lake. The highest prevalence values occurred in the eastern basin less densely populated with eels, while in the western basin a large proportion of the fish were free of infection. Helminth-free status accompanied by thickening of the swimbladder wall developed after intensive infections. In 1991, eel mortality could be observed only in the western basin. In 1992, the number of eels with swimbladders having a thickened wall but not containing helminths increased also in the central and eastern areas of the lake. Parallel to this, a mortality less expressed than the one in 1991 occurred in the central part of the lake. By 1993, a host-parasite equilibrium had become established in Lake Balaton.
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).
Ninety-five eels from one marine and three freshwater localities in Iceland were examined for parasites. Twenty species were found, 12 from marine habitat, 12 from freshwater and 4 species were found in both habitats. These are: Eimeria anguillae, Chilodonella hexasticha, Trichodina fultoni, T. jadranica, Myxidium giardi, Myxobolus kotlani, two Zschokkella spp., Derogenes varicus, Deropristis inflata, Diplostomum sp., Plagioporus angulatus, Podocotyle atomon, Anisakis simplex (larva), Eustrongylides sp. (larva), Hysterothylacium aduncum (larva), Raphidascaris acus (larval and adult stages), Bothriocephalus claviceps, Proteocephalus macrocephalus, and a pseudophyllidean larva. Thirteen of these species are new parasite records from Icelandic waters. The component community of marine eels was characterized by low diversity and a high dominance of a single species. Overall, seven species of helminths were observed, up to five different species occurring in an individual fish. The component community of the freshwater eels was species-poor with low diversity and relatively high dominance of single species. A between-sites difference in the freshwater eels was considerable; only Diplostomum sp. was found at more then one sampling site. Similar to previous studies, there is a total replacement of freshwater macroparasite species by marine ones in saline waters. But unlike research abroad in which species richness decreases with higher salinity, the marine eels in Iceland have considerably higher richness than the freshwater ones. The parasite communities of freshwater eels in Iceland are, in general species-poorer, less diverse and having higher Berger Parker (BP) dominance than other eel communities in Europe. Marine eels have on the other hand comparable species richness, are less diverse and with a high BP dominance.
Analysis of the stomach contents of otters recovered from South West England between 1999 and 2003 revealed that prey items taken were principally species of fish and amphibians, with mammals and birds occasionally taken. The fork length of fish recorded was 30 to 720 mm. Eel Anguilla anguilla was the dominant prey item, with up to five present per stomach. Estimated lengths ranged from 100 to 450 mm. Other common prey items were bullhead Cottus gobio and brown trout Salmo trutta. In addition to these freshwater species, there were recordings of sea bass Dicentrarchus labrax and thick lipped mullet Chelon labosus, indicating foraging in both freshwater and marine habitats. A seasonal peak was observed in the relative frequency of amphibians in diet, as otters took advantage of spawning aggregations. However, there were no seasonal trends in the relative frequency of other species in otter diet, with eel, bullhead and cyprinid species taken regularly in all months.
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.
Daniconema anguillae Moravec et Koie, 1987 larvae measuring 1.64-1.76 mm were occasionally found in considerable numbers in the fins and subcutaneous connective tissue of approximately 50% of eel Anguilla anguilla (L.) sampled from Lake Balaton, Hungary. The larvae were noted for their slender body, very long tail with a rounded tip, a densely transversely striated cuticle, and the presence of boring tooth and large kidney-shaped amphids on the cephalic end. The larvae could easily be recovered from the above mentioned organs by placing them into isotonic saline solution. No disease signs or pathological changes attributable to the larval infection could be observed. The only histological indication of host reaction was the appearance of macrophages adhering to the body surface of larvae and of cells with spherical nucleus in areas around the larvae. A possible life cycle pattern of I), anguillae is discussed.