Sixteen labrid species, including four Bodianus spp., were examined in New Caledonia (South Pacific) and monogeneans were found only on Bodianus perditio (Quoy et Gaimard). This species, Haliotrema banana sp. n., is the second Haliotrema species to be described from the labrids, the first being Haliotrema bodiani Yamaguti, 1968 from Bodianus albotaeniatus (Valenciennes), previously designated as B. bilunulatus (Lacépède). The new species is similar to H. bodiani in soft reproductive parts but differs from it in the morphologies of the hard haptoral parts, mainly in the shape of the dorsal bar (bar-shaped vs V-shaped in H. bodiani) and ventral bar. It is similar to Haliotrema spirale Yamaguti, 1968 and Haliotrema minutospirale Yamaguti, 1968 in the shape of the anchors and bars but differs from them in the detailed structures of the copulatory organ and vaginal system.
Heliocotyle ewingi sp. n. (Monogenea: Monocotylidae) is described from the gills of Myliobatis australis Macleay, 1881 (Myliobatididae) collected from Norfolk Bay near Hobart, Tasmania, Australia. Heliocotyle ewingi can be distinguished readily from the only other species in the genus, Heliocotyle kartasi Neifar, Euzet et Ben Hassine, 1999, by the presence of a single pseudoseptum on each of the peripheral loculi except the posteriormost, eyespots and by the morphology of the male copulatory organ which is a short, straight sclerotised tube which lacks a sclerotised accessory piece. The generic diagnosis is revised to accommodate the new species and the anterior glands are discussed.
Just nineteen species of ectoparasitic helminths were found in a survey of over 1,500 individuals of 26 species of sillaginid fishes in the Indo-west Pacific, A twentieth worm is known only from the literature; a twenty-first, also known only from the literature, is considered a doubtful record. Fifteen of the twenty worms are branchial monogeneans, one is a monoge-nean of the pharyngeal plates, one is an ectoparasitic digenean living under the scales, and three are leeches of the mouth cavity and fins. The most common monogeneans were diplectanids (Diplectanum spp. and Monoplectanum spp.) and microcotylids (Polylabris spp.), each with five recently described or redescribed species. Of the remaining monogeneans, three were extremely rare, and two were uncommon. Pseudnbivagina sp. and Polynemicola sp. (Microcotylidae) and Pseudempleurosoma sp. (Ancyrocephalidae) were represented by only a single worm each from three different hosts (Sillago robusta, S. sihama, and S. ingenuua, respectively). The gyrodactylid Gyrodactylus sp, is widespread and was recorded from four species of sillaginids (S. ciliata, S. japonica, S. schomburgkii and S. sihama). Encolyllabe chirrmemi Robinson (Capsalidae) is recorded for the first time from sillaginids, but only on S. aeolus.'Tv/o additional monogeneans are known from sillaginids only in the literature: Dacty-logyrus sp, (Dactylogyridae) is known only from cultured S. sihama', the single specimen of Microcotyle sp. (Microcotylidae) recorded from Sillaginodes punctata is probably a contaminant, since the haptor was missing. The generalist trematode Trans-versolrema Ucinum Manter (Transversotrematidae) was found for the first time in samples of four species of sillaginids (Sillago analis, S. ingenuua, S. lutea and 5. sihama). Three species of piscicolid leeches were encountered: Austrohdella translucens Badham was common on the fins of three large inshore sillaginids (S. ciliata, S. schomburgkii and S. analis); a single specimen of the generalist species Zeylanicobdella arugamensis De Silva was recovered from S. soringa·, and specimens of Z. stellata (Moore) infected S. schomburgkii and S. analis. The diversity of host-specific worms in Sillaginidae is low compared with those of some other Indo-west Pacific fishes.
Differences in the occurrence of monogeneans on lamellae of fish gill arches were observed in this study. These differences were attributed to variations in water current on the gill surfaces or to greater area of certain arches. Two computer simulation programs based on gill area and water current were written to generate parasite melapopulations with clumped patterns. The results obtained were compared with true distributions of selected freshwater monogenean taxa. The combination of both theoretical models (gill area and water current) had greater explanatory power than either of the models alone.
Host responses against skin inhabiting monogeneans are commonly obserÇetHtflfthe responsible immune mechanisms in the fish skin are insufficiently described. Based on recent knowledge of fish immunity and skin response mechanisms in mammals a model for the skin immunity in fish to monogcnean infections is proposed. Important cellular components of the model are the epithelial cells, the mucous cells and leucocytes. The release of cytokines, e.g. IL-1, following mechanical or chemical injury of the epithelial cells, initiates a series of events leading to decrease of the ectoparasite population. Cytokines (e.g. IL-1, TNF, INF) are suggested to affect secretions from mucous cell and attract neutrophils and macrophages. Leukotrienes are probably involved in the inflammatory reactions. The subsequent production of humoral substances (among others complement factors and peptides) could be responsible for the antiparasitic response in the later stages of infection. Although non-specific factors dominate the response, the involvement of specific antibodies and lymphocytes cannot be excluded.
Parasites with high host specificity maximally depend on their hosts, which should increase the likelihood of coevolution. However, coevolution requires reciprocal selection exerted by the host and the parasite, and thus a considerable level of parasite virulence. In species of the monogenean ectoparasite genus Gyrodactylus consecutive generations are confronted with a single host, which may constrain the evolution of virulence. Transmission, which is often important in the ecology of Gyrodactylus species, may have the opposite effect, but may also lead to the avoidance of coevolutionary arms races. We investigated the potential outcome of coevolution between Gyrodactylus gasterostei Gläser, 1974 and its host, the three-spined stickleback (Gasterosteus aculeatus L.) by determining the strength of genotype by genotype (G×G) interactions on two levels: within and between sympatric and allopatric host populations. To do so, we compared the parasite's infection dynamics on laboratory-reared sympatric (Belgian) and allopatric (German) hosts. We found that a parasite line successfully infected a range of sympatric host genotypes (represented by families), while it failed to establish on allopatric hosts. Phylogeographic studies suggest that neutral genetic divergence between the host populations cannot explain this dramatic difference. Provided that this result can be generalised towards other parasite lines, we conclude that coevolution in this host-parasite system is more likely to lead to local adaptation on the population level than to G×G interactions within populations.
Lamellodiscus dentexi Aljoshkina, 1984, a gill parasite of Dentex macrophthalmus (Bloch), is redescribed based on new material from the northwest coast of Africa (Senegal and Morocco). Three new species of Lamellodiscus Johnston et Tiegs, 1922 from D. macrophthalmus are described, Lamellodiscus toguebayei sp. n., L. vicinus sp. n., and L. triacies sp. n., all belonging to the ''ignoratus'' group. They can be distinguished from all other species of this group by the size and shape of male copulatory organ and sclerotised parts of the haptor. Considering the peculiar morphology of the male copulatory organ (long and thin tube) we propose to put together L. dentexi, L. virgula Euzet et Oliver, 1967 and L. obeliae Oliver, 1973 to form the ''elongatus'' type within the ''elegans'' group.
The gills of 63 specimens of the Atlantic bluefin tuna Thunnus thynnus (Linnaeus) (Osteichthyes: Scombridae) from three localities of the Mediterranean (Sardinian, Tyrrhenian and Levantine Seas) were examined for metazoan parasites. The parasite fauna of T. thynnus from the Sea of Sardinia included 11 species: five didymozoid trematodes, three capsalid and one hexostomid monogeneans, and one caligid and one pseudocycnid copepods. Four didymozoids were found in fish from the Levantine Sea and only one didymozoid was recorded in fish from the Tyrrhenian Sea. Dividing the hosts into four size-groups (small, medium-sized, large and extra large), the pairwise comparison of prevalence and mean abundance of the new and literary data) showed differences according to host size. The differences in the composition of the parasitic faunas and in the prevalence of parasites, observed between the small tunas from the Tyrrhenian Sea and the medium-sized tunas from the Adriatic Sea, Levantine Sea and the North-East (NE) Atlantic Ocean, indicated that these groups form discrete units. The parasite fauna of the large tunas from the Sea of Sardinia is the richest among the bluefin tuna populations of the Mediterranean and the NE Atlantic, due to the presence of species not found elsewhere in bluefin tunas, such as Caligus coryphaenae Steenstrup et Lütken, 1861, Capsala magronum (Ishii, 1936) and C. paucispinosa (Mamaev, 1968). This fact and the prevalence of some parasites of this group (lower than those of medium-sized fish from the NE Atlantic and higher than the small and medium-sized tunas from the Mediterranean) suggest that the large-sized tuna group in the western Mediterranean is formed by Mediterranean resident tunas (poorly infected), and by tunas migrating from the Atlantic Ocean (heavily infected).
Microhabitat preference of the monogenean Discocotyle sagittata (Leuckart, 1842) was determined in late spring and late autumn in rainbow trout, Oncorhynchus mykiss (Walbaum), reared in the Isle of Man, UK. Discocotyle sagittata exhibits a preference for attachment to anterior gill arches: 29% of all worms occurred on gill arch I, 28% on II, 25% on III and 18% on IV. This distribution pattern on the introduced salmonid species is the same as reported for its native European host, the brown trout Salmo trutta (L.). Previous experimental work suggested that invasion is a passive process followed by post-invasion migration to anterior gill arches; the present work provides evidence of equivalent site selection taking place in fishes maintained under conditions promoting continuous reinfection in aquaculture. Migration may be density-dependent, since a significant inverse association was found between the intensity of mature parasites and their proportion on anteriormost gill arch I.
A study on the spatial distribution of two congeneric monogenean species Pseudodactylogyrus anguillae Yin ct Sproston, 1948 and P. bini Kikuchi, 1929 on the gills of large size European eel Anguilla anguilla (L.) were conducted. Results were analysed with regard to: single-species infection, mixed infection and general occurrence of the parasites in the ccl population. Statistical analysis revealed that the distribution of these species on the gill apparatus is fairly similar and the zones in which they occur more numerously coincide to a great extent. However, a number of differences were found. Both the possibility of simultaneous occurrence on Ihe host and similar distribution of the above species on the eel’s gills indicate the reciprocal tolerance of these parasites.