A new species of the cyclopoid copepod genus Ergasilus von Nordmann, 1832 is described based on adult female specimens removed from the gills of the yellow snapper Lutjanus argentiventris (Peters) and the yellowfin snook Centropomus robalito Jordan et Gilbert from a Pacific coastal system of Mexico. The new species Ergasilus davidi sp. n. has a combination of characters that includes a two-segmented first leg endopod, a three-segmented fourth leg endopod, and the presence of a single seta on the first antennular segment. These characters are shared with 14 other congeners known mainly from Brazil and North America. It differs from these other species in the armature and ornamentation of legs 1 and 4, the shape of the body, and the structure and ornamentation of the antennae. Additional characters include a maxillar basis armed with blunt teeth, distally bent maxillular setae, and naked margins of first exopodal segments of legs 2-4. Previous regional records of Ergasilus sp. from both fish species are probably assignable to E. davidi. The prevalence and intensity of infection was estimated for both teleost species and agrees to previous data. Based on other records of the genus from several other teleost species in the surveyed area and adjacent zones of the Eastern Pacific, it is presumed that the new species could have a wider range of hosts. The new species represents the first Ergasilus described from Mexican waters of the Pacific. Overall, the genus remains poorly known in Central America and Mexico.
Over a 7-year period, parasites have been collected from 28 species of groupers (Serranidae, Epinephelinae) in the waters off New Caledonia. Host-parasite and parasite-host lists are provided, with a total of 337 host-parasite combinations, including 146 parasite identifications at the species level. Results are included for isopods (5 species), copepods (19), monogeneans (56), digeneans (28), cestodes (12), and nematodes (12). When results are restricted to those 14 fish species for which more than five specimens were examined and to parasites identified at the species level, 109 host-parasite combinations were recorded, with 63 different species, of which monogeneans account for half (32 species), and an average of 4.5 parasite species per fish species. Digenean records were compared for 16 fish species shared with the study of Cribb et al. (2002); based on a total of 90 parasite records identified at the species level, New Caledonia has 17 new records and only seven species were already known from other locations. We hypothesize that the present results represent only a small part of the actual biodiversity, and we predict a biodiversity of 10 different parasite species and 30 host-parasite combinations per serranid. A comparison with a study on Heron Island (Queensland, Australia) by Lester and Sewell (1989) was attempted: of the four species of fish in common and in a total of 91 host-parasite combinations, only six parasites identified at the species level were shared. This suggests strongly that insufficient sampling impairs proper biogeographical or ecological comparisons. Probably only 3% of the parasite species of coral reef fish are already known in New Caledonia.
A new species of parasitic copepod, Chondracanthus hoi sp. n. (Copepoda: Chondracanthidae), is described based on specimens of both sexes collected from the buccal cavity and gill arches of the silvery john dory, Zenopsis conchifer (Lowe) (Zeiformes: Zeidae), from waters off northern Argentina (35-36°S, 53-54°W). Female of C. hoi differs from its congeners by the following combination of characters: presence of five pairs of trunk processes, antennule with four knobs tipped with small setae and absence of denticles on the terminal process of maxilla. Chondracanthids and zeiform fishes have been proposed as an example of co-speciation; this assumption is derived from a series of analyses based on incomplete records of both geographical distribution and host range of some parasite species, as well as misidentification of fish hosts. These inconsistences observed during our bibliographical analyses are also discussed.
Caligus mortis Kensley, 1970 was originally described from females collected from intertidal pools along the coast of Namibia. During surveys at Jeffreys Bay and De Hoop Nature Reserve in South Africa, both females and males of C. mortis were collected from intertidal pool fish hosts. Based on this material a full description of the male is given, and a comparison with the female reveals the sexual dimorphic characteristics.
The development of the nematode Procamallanus saccobranchi Karve, 1952, a parasite in the stomach of the fish Heteropneustes fossilis (Bloch), was studied in Mesocyclops crassus (Fischer) and Mesocyclops leuckarti (Claus). After being ingested by the copepods the nematode first-stage larvae penetrated into the haemocoel of the intermediate host; there they moulted twice (on days 3 and 5 p.i. at 28-30°C) attaining the third, infective stage. The definitive host H. fossilis acquired infection by feeding on copepods harbouring infcclivc-stage larvae; in the stomach of this definitive host, the larvae were observed to undergo two more moults. The third moult occurred on day 13 p.i. and the fourth moult on day 38 p.i. and day 66 p.i. in “male” and “female” larvae, respectively. The larval stages, including the moulting forms are described and illustrated.
Copepods of the genus Achtheinus Wilson, 1908 (Pandaridae) are parasites of elasmobranchs that attach to their fins, gill slits and around the nostrils. Specimens of Achtheinus pinguis Wilson, 1912 were collected and examined using histology and scanning electron microscopy to determine their way of attachment to the host and the possible effect on the host. They insert their antennae deep into the dermis of the shark's skin, which causes the most damage due to possible tissue compression and/or fibrosis as well as rupture of the connective tissue. Additionally, the presence of the copepod on the skin causes cell erosion of the epidermal cells and thus reduces the number of epidermal layers. The maxillipeds are used to attach to the placoid scales that cover the shark's skin and probably serve to keep the copepod and inserted antennae in position. This is accomplished by the insertion of the placoid scales into the flaccid corpus of the maxillipeds. Observed damage seems to be negligible to the shark apart from the possibility of secondary infection., Susan M. Dippenaar, Anine Jordaan., and Obsahuje bibliografii
Larval development of the nematode Onchocamallanus bagarii (Karve et Naik, 1951), recovered from the intestine of the fish Bagarius bagarius (Hamilton) was studied under laboratory conditions. The cyclopoid copepods Mesocyclops leuckarti (Claus) and M. crassus (Fischer) were infected with first-stage larvae from female uteri and maintained at temperatures 29-30°C. After being swallowed by the copepods, first-stage larvae burrow through the intestinal wall and reach the haemocoel of the copepods and there they grow and moult twice to attain the third and infective-stage. First-stage larvae become ensheathed after 65 hours of infection and second-stage larvae first appeared on day 3 post infection (p.i.). The second moult occurred on day 5 p.i. The larval stages occurring during development are described.
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).
The developmental stages and life cycle of the nematode Camallanus anabantis Pcarse, 1933 an intestinal parasite of Anabas testudineus (Bloch) arc described. The copepod Mesocyclops leuckarti (Claus) was used as experimental intermediate host. After being ingested by the copepods the nematode first-stage larvae enter its haemocoel, where they moult twice, 4 d.p.i. and 11 d.p.i., at 21-26°C, respectively to become the infective third-stage larvae. The definitive fish hosts become infected when feeding on copcpods harbouring infective larvae. In the fish host’s intestine the larvae undergo two more moults, the third on day 15 p.i. The fourth moult of “male” larvae occurred on day 68 p.i. and that of “female” larvae on day 86 pi. at water temperatures 24-36°C- A female with eggs and few larvae in the uteri was first observed on day 187 p.i.
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.