The adults of Trichosurolaelaps dixous Domrow, 1972 are redescribed from a population of Trichosurus cunninghami Lindenmayer, Dubach et Viggers, 2002 in south-eastern Australia. The nymphal stages are described for the first time. Morphologically, T. dixous is similar to Trichosurolaelaps crassipes Womersley, 1956. Morphological differences between the pre-female deutonymphs and adult females of the two mite species are the presence of a single large ventral spur on tibia I of T. dixous. Males of T. dixous could not be distinguished from T. crassipes morphologically and the idiosomal length of male T. dixous was variable (475-683 μm). Protonymphs of the two mite species differed only in size, with that of T. dixous being larger. Although T. crassipes was prevalent in a sympatric population of Trichosurus vulpecula and has been reported from other populations of T. cunninghami in southern Australia, it was never recovered from the population of T. cunninghami studied.
Paramoniezia suis Maplestone et Southwell, 1923 is redescribed from the type and only specimen, and is considered to be a genus inquirendum and species inquirenda, possibly based on a host misidentification. Paramoniezia phacochoeri Baylis, 1927 is redescribed from new material from Phacochoerus africanus (Gmelin) from South Africa and is transferred to Moniezia Blanchard, 1891 as M. phacochoeri (Baylis, 1927) comb. n. A redescription of M. mettami Baylis, 1934, also from Ph. africanus, establishes the independence of the two congeneric species parasitizing warthogs. A new genus, Phascolocestus, is erected for Paramoniezia johnstoni Beveridge, 1976 from vombatid marsupials as Phascolocestus johnstoni (Beveridge, 1976) comb. n., and additional host and distributional data are provided for this species.
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 Nybelinia Poche, 1926, N. queenslandensis sp. n. (Cestoda: Trypanorhyncha) is described from sharks, Carcharhinus melanopterus (Quoy et Gaimard, 1824) from the coast of northeastern Queensland, Australia. Morphological features of the 46 known species of Nybelinia Poche, 1926 are tabulated and the new species is differentiated from all known taxa that are adequately described on the basis of having a homcomorphous armature, metabasal hooks 20-25 pm long, tentacles 0.07-0.09 mm in diameter, short bulbs (0.38-0.45 mm) and craspedote segments with the testes encircling the female genital complex. The fine structure of the scolex microtriches, frontal and rhynchodeal glands, tentacles and hooks, sheath and retractor muscle is described and compared with that of other trypanorhynchs.
A new species of Prochristianella Dollfus, 1946 is described from the spiral intestine of the wedgenose skate, Dipturus whitleyi (Iredale) (Rajiformes: Rajidae), off the north-western coast of Tasmania (Australia). Prochristianella mattisi sp. n. is characterised by an acraspedote scolex, two oval bothria, elongate, bent bulbs, a retractor muscle inserting at the base of each bulb and the presence of gland-cells within the bulbs and prebulbar organs. The tentacular armature is typical heteroacanthous, heteromorphous, with a characteristic basal oncotaxy and a metabasal armature with hooks first increasing and then decreasing in size along each principle row. It can be differentiated from other species of Prochristianella by a combination of morphological characters, such as the metabasal tentacular armature with eight hooks per principle row, a unique basal armature without enlarged hooks on the basal swelling and genital pores slightly posterior to the mid-line of the segment. The description of P. mattisi sp. n. increases the number of known species within Prochristianella to 20, eight of which occur in Australian waters. A key for the identification to species within Prochristianella is provided.
Progrillotia pastinacae Dollfus, 1946 (Cestoda: Trypanorhyncha) is redescribed from the spiral valve of Dasyatis pastinaca (Linnaeus) (Dasyatididae) from the coast of France. Progrillotia dasyatidis sp. n. is described from the spiral valves of Dasyatis tortonesei Capapé (Dasyatididae) from the Mediterranean in the Gulf of Gabès (Tunisia) and D. pastinaca from the Bassin d'Arcachon (France). The new species differs from congeners in having, on the tentacles, a single rather than two rows of intercalary hooks and fewer testes. The generic definition is emended based upon the new species, the redescription of P. pastinacae Dollfus, 1946 and re-examination of the type specimen of P. louiseuzeti Dollfus, 1969. Important additional characters noted are that the tentacular hooks are solid, a prebulbar organ is present and that there are gland cells attached to the retractor muscle within the bulb. A cladistic analysis suggests that the genus is closely allied with the Eutetrarhynchidae. Progrillotia dollfusi Carvajal et Rego, 1983 is provisionally excluded from the genus as the adult of the species is unknown and a key character of the genus is that the testes are pre-ovarian.
The family Rhopalothylacidae (Cestoda: Trypanorhyncha) is reviewed. The type species, Rhopalothylax gymnorhynchoides Guiart, 1935, is redescribed from the type specimens and belongs within the genus Pintneriella Yamaguti, 1934, previously described only from the plerocercus. Rhopalothylax therefore becomes a junior synonym of Pintneriella. The adult of Pintneriella musculicola Yamaguti, 1934 is described for the first time, from the shark Carcharias taurus Rafinesque from Australia. Pintneriella is characterised by two bothridia, a typical heteroacanthous armature, a unique, bipartite external seminal vesicle and a uterus deviated porally, terminating at a uterine pore. It belongs within the Heteracanthoidea but is distinguishable both from the Eutetrarhynchidae and the Gilquiniidae, the two families which it most closely resembles. Cladistic analyses align Pintneriella within the clade containing the families Gilquiniidae, Gymnorhynchidae and Molicolidae rather than with the Eutetrarhynchidae. The family Rhopalothylacidae is therefore retained provisionally to accommodate Pintneriella within the Heteracanthoidea. The second genus of the Rhopalothylacidae, Clujia Guiart, 1935, is unrecognisable from its description and cannot be redescribed from its holotype. It is therefore considered a genus inquirendum.
Three new genera of eutetrarhynchid trypanorhynch cestodes are described from Mobula spp. (Mobulidae) from the Gulf of California, Mexico. Fellicocestus mobulae gen. et sp. n. from the gall bladder of Mobula japonica (Müller et Henle) is distinguished by elongate bothria, a pars bothrialis equal in length to the pars vaginalis, masses of gland cells in the pars vaginalis and an heteromorphous armature in which hook rows arise from a central file of hooks on the bothrial surface of the tentacle and terminate in a central file on the antibothrial surface. Species of Mobulocestus gen. n. occur in the nephridial system and cloaca of rays and are characterized by two bothria, an heteroacanthous armature with hook rows beginning on the bothrial surface and terminating on the antibothrial surface, and by hooks at the beginnings of rows with an apical cavity. M. nephritidis sp. n. and M. lepidoscolex sp. n., both from the nephridial system of Mobula thurstoni (Lloyd) are differentiated by testis number and by the presence of scale-like microtriches on the tegument of the scolex of M. lepidoscolex. M. mollis sp. n., from the cloaca of Mobula thurstoni is distinguished by testis number (97-111 in M. lepidoscolex, 20-22 in M. nephriticus and 48-70 in M. mollis). Hemionchos gen. n. from the spiral valve of Mobula spp. has two bothria, an heteroacanthous armature, hook rows arising on the bothrial surface and terminating on the antibothrial surface and hooks at the beginning of rows with an apical cavity. It differs from Mobulocestus in having a distinctive basal armature and both hook files 1 and 1' on the bothrial surface, but has an additional, small, satellite hook adjacent to each hook 1'. H. striatus sp. n. from the spiral valve of Mobula thurstoni and M. japonica is differentiated by having a basal armature of closely packed arrays of small, uncinate hooks. H. mobulae sp. n. from the spiral valve of Mobula japonica and M. munkiana Notarbartolo di Sciari, differs in testis number and in having large, flattened hooks in the basal armature. H. maior sp. n., from the spiral valve of M. japonica, is larger, differing in both the number of testes and in the basal armature.