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A checklist of literature records of the digenean parasites of macrourids from the world’s oceans is given. Where necessary annotations discussing the validity of the records are included. In addition, the records are listed under host. Tables summarising (I) the occurrence of parasites families, and (II) the geographical distribution of parasite species, are included. A figure illustrating the bathymetry of the parasite species is given. Information from 84 papers is summarised, in cluding records from 49 host-species and 13 genera. 68 identified species of adult worm, from 29 genera and 12 families and are reported. The most frequently reported families are the Lepocreadiidae, Derogenidae and Hemiuridae. The most frequently reported genus is Lepidapedon. Worms are reported from macrourids a depths between 150 and 7,000 m, with five identified species reported from the north-eastern Atlantic abyssal plain at a depth of about 4,850 m.
W listopadzie 2009 roku w potoku Rzepnik, w dopływie Skawinki (dorzecze Górnej Wisły), odłowiono 5 kiełbi białopłetwych Romanogobio albipinnatus complex. Ryby te preferują duże nizinne rzeki, dlatego nowe stanowisko w zaledwie 10-kilometrowym cieku o szerokości koryta wynoszącej 2–3 m jest bardzo nietypowe. Jest to pierwsze stwierdzenie kiełbia białopłetwego na terenie Małopolski
Lecithostaphylus tylosuri sp. nov. (Digenea, Zoogonidae) specimen were collected from the digestive tract of Tylosurus acus imperialis (Teleostei, Belonidae) caught off the eastern coast of Tunisia. L. tylosuri is very similar to its closest relatives, L. retroflexus and L. nitens. It can be easily distinguished from L. retroflexus (Molin, 1859) in having a more extensive vitellarium, with follicles reaching from the posterior margin of the acetabulum and extending beyond the posterior margin of the testes and a coiled seminal vesicle. L. tylosuri differs from L. nitens as illustrated by Linton 1898, in having a longer cirrus pouch (0.7 mm vs 0.36 mm, respectively) overlapping the anterior edge of the ventral sucker and a submarginal genital pore (submedian in L. nitens). It’s also different from L. nitens as described by Manter 1947 in the vitelline disposition and in having the greater sucker ratio (1: 1.3–2.1 vs 1: 1.3–1.6, respectively). L. tylosuri differs from L. nitens as reported by Machida and Kuramochi 2000 by the absence of variations in the vitellarium disposition in all specimens. L. tylosuri is more similar to L. nitens from group A (considered synonym of L. ahaaha Yamaguti, 1970 = L. nitens by Bray 1987) by having vitelline follicles extending beyond the testes. L. tylosuri can be distinguished from L. ahaaha by its pedunculate rather than prominent acetabulum and its larger body size (4.10–7.85 mm long and 0.75–1.2 mm large vs 2.1–6 mm long and 0.45–1.1 mm large, respectively). The prevalence of L. tylosuri sp. nov. was negatively correlated with host length (decreasing with host size increasing). Host sex does not seem to affect infection parameters.
Between May and September 2006, 640 specimens of the rabbitfish Siganus rivulatus Forsskål (Teleostei, Siganidae) were examined for infections with intestinal helminths. These fishes were caught in the Red Sea off the coast of Sharm El-Sheikh, South Sinai, Egypt, examined in a field laboratory and separated into three size groups of regular length intervals. Only three species of helminths were recovered: the trematode Gyliauchen volubilis Nagaty, 1956 (Gyliauchenidae Fukui, 1929), the acanthocephalan Sclerocollum rubrimaris Schmidt et Paperna, 1978 (Cavisomidae Meyer, 1932) and the nematode Procamallanus elatensis Fusco et Overstreet, 1979 (Cucullanidae Cobbold, 1864). The distribution of these helminths along the intestine of S. rivulatus, in all patterns of single and concurrent infections and the corresponding prevalences and intensities of infection in the different size groups of the fish were recorded. In single infections, each parasite species was found distributed in a well-defined fundamental niche along the intestine of Siganus rivulatus, and a distinct partial overlap between the niches of G. volubilis and Sclerocollum rubrimaris was observed. In concurrent infections with these two species, their fundamental niches were significantly reduced, probably being affected by interactive site segregation and individuals of each species were found segregated in a restricted realised niche. In all other patterns of concurrent infections, each parasite species was normally found in its original fundamental niche. The prevalences of these parasites in the fish examined were relatively low and somewhat similar. In all patterns of single and concurrent infections, the intensity of infection was directly related to fish size. In concurrent infection with G. volubilis and S. rubrimaris, a significant decline was observed in the intensities of both species in the different size groups of the fish, but, in all other patterns of concurrent infections, no significant change in intensity was observed. These observations suggest that the interaction between G. volubilis and S. rubrimaris is probably a negative and symmetrical one. The mode of transmission of these parasites to the fish is also discussed.
We propose to name as Lamellodiscus theroni sp. nov., the gill parasite of Diplodus puntazzo (Cetti) that was reported by Euzet (1984) as L. ergensi Euzet and Oliver, 1966 in Kerkennah Island (Tunisia). L. theroni sp. nov. was also found specific to D. puntazzo in Algiers Bay (Algeria) and in Gulf of Lion (France). The host specificity of various Lamellodiscus species on D. puntazzo is briefly discussed. Within Lamellodiscus, L. theroni belongs to the “ignoratus” group characterized by a “lyre” shaped male copulatory organ and to the “ergensi” subgroup, characterized by a complex morphology of the haptoral dorsal bars. L. theroni differs from the five other species of this subgroup (L. ergensi, L. kechemirae, L. tomentosus, L. sanfilippoi, L. baeri) by the morphology and the size of the haptoral dorsal bar. L. theroni, as well as, L. hilii, L. bidens, L. impervius, was only reported on the sparid Diplodus puntazzo. These parasite species are all considered as oioxenic.
Spermiogenesis in Helicometra fasciata is characterized by an unusual flagellar rotation. Indeed, a rotation of the axonemes, higher than 90°, occurs. Nevertheless, the general pattern is the same as in the other digenean trematodes examined. The zone of differentiation presents striated rootlets associated with two centrioles, and an intercentriolar body. The nucleus and mitochondrion migrate in the median cytoplasmic process. An asynchronic proximo-distal fusion takes place. The mature spermatozoon possesses five regions and two axonemes with the 9 + ‘ 1 ’ pattern, nucleus, mitochondrion, glycogen granules and two bundles of parallel cortical microtubules. Despite these features, there are some other peculiarities that distinguish the spermatozoon of H.fasciata. A centriolar derivative and a lateral expansion were observed in the anterior region. To discuss the phylogenetic relationships, comparison is made with Opecoeloides furcatus, the only other opecoeloid for which the reproduction characters were described.
Morphological data for Acanthocephaloides propinquus (Arhythmacanthidae) from gobiid fishes from the northwestern Black Sea are presented. Individuals from the Black Sea differ from the descriptions based on Mediterranean specimens in having 4–5 proboscis hooks per row in the former and 5–6 in the latter. The size of the cuticular spines is rejected as a diagnostic character for A. propinquus because their length varies in a wide range (3.0–7.5 µm). The diagnostic characters for identifying A. propinquus include the presence of small culticular spines, the testes located in the central part of the body and an acanthor having a single hooklet lacking a root.
Lamellodiscus crampus sp. nov. (Monogenea, Diplectanidae) is described from the gills of Dentex maroccanus (Valenciennes) collected from the Gulf of Gabès (Tunisia) in the oriental part of Mediterranean Sea. The new species belongs to the “ignoratus” group (sensu Oliver 1987) characterized by a lamellodisc with complete lamellae and a “lyre” shaped male copulatory organ, and the “ignoratus” sensu stricto subgroup, characterized by a haptor with simple lateral dorsal bars, as proposed by Amine and Euzet (2005). Lamellodiscus crampus can be easily distinguished from all the congeneric species of the subgroup “ignoratus” by the presence, in the “lyre” male copulatory organ, of five spines in the distal portion on the axial side of the paired piece.
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