ORCID Profile
0000-0002-6097-0696
Current Organisations
University of Queensland
,
South Australian Museum
Does something not look right? The information on this page has been harvested from data sources that may not be up to date. We continue to work with information providers to improve coverage and quality. To report an issue, use the Feedback Form.
Publisher: Springer Science and Business Media LLC
Date: 06-2002
Abstract: Several heteracanthocephalid specimens were recovered from the flatfish Rhombosolea leporina (Günther), a host of Heteracanthocephalus peltorh hi (Baylis, 1944) Petrochenko, 1956 from New Zealand. Unlike H. peltorh hi, these new specimens have trunk spines. Measurements and proboscis armament of the new specimens are consistent with the worms being Aspersentis minor Edmonds & Smales, 1992 originally described from the Australian flounder Rhombosolea tapirina Günther. A review of the family Heteracanthocephalidae Petrochenko, 1956 was undertaken to assess the validity of its four genera and eight species. The validity of Aspersentis megarhynchus (Linstow, 1892) Golvan, 1960 (syn. Echinorhynchus megarhynchus Linstow, 1892) is questioned. E. megarhynchus is not considered to be an heteracanthocephalid and is relegated to a species inquirenda. A. megarhynchus (Linstow, 1892) of Golvan (1960) nec E. megarhynchus Linstow, 1892 is considered a synonym of A. austrinus Van Cleave, 1929. The monotypic genus Heteracanthocephalus Petrochenko, 1956 is proposed as a synonym of Aspersentis Van Cleave, 1929 because there appear to be insufficient morphological differences between them. Aspersentis peltorh hi n. comb. is proposed for Heteracanthocephalus peltorh hi. The monotypic genus Sachalinorhynchus Krotov & Petrochenko in Petrochenko, 1956 is considered valid, but the other heteracanthocephalid genus, Bullockrhynchus Chandra, Rao & Shyamasundari, 1985, also monotypic, is not. B. indicus Chandra, Rao & Shyamasundari, 1985 possesses more features resembling rhadinorhynchids than heteracanthocephalids but only females are known, and therefore the genus and species cannot be placed. There are currently four valid species of Aspersentis and one of Sachalinorhynchus.
Publisher: Springer Science and Business Media LLC
Date: 03-1998
Publisher: Elsevier BV
Date: 12-2000
DOI: 10.1016/S0020-7519(00)00121-1
Abstract: Recruiting coral reef fish larvae from 38 species and 19 families from New Caledonia were examined for parasites. We found 13 parasite species (Platyhelminthes: Monogenea, Cestoda and Trematoda) but no acanthocephalan, crustacean or nematode parasites. Over 23% of in idual fish were infected. Didymozoid metacercariae were the most abundant parasites. We conclude that most of the parasites are pelagic species that become 'lost' once the fish larvae have recruited to the reef. Larval coral reef fish probably contribute little to the dispersal of the parasites of the adult fish so that parasite dispersal is more difficult than that of the fish themselves.
Publisher: Cambridge University Press (CUP)
Date: 24-09-2002
DOI: 10.1017/S0031182002001671
Abstract: Groupers (Epinephelinae) are prominent marine fishes distributed in the warmer waters of the world. Review of the literature suggests that trematodes are known from only 62 of the 159 species and only 9 of 15 genera nearly 90% of host–parasite combinations have been reported only once or twice. All 20 families and all but 7 of 76 genera of trematodes found in epinephelines also occur in non-epinephelines. Only 12 genera of trematodes are reported from both the Atlantic–Eastern Pacific and the Indo–West Pacific. Few (perhaps no) species are credibly cosmopolitan but some have wide distributions across the Indo–West Pacific. The hierarchical ‘relatedness’ of epinephelines as suggested by how they share trematode taxa (families, genera, species) shows little congruence with what is known of their phylogeny. The major determinant of relatedness appears to be geographical proximity. Together these attributes suggest that host-parasite co-evolution has contributed little to the evolution of trematode communities of epinephelines. Instead, they appear to have arisen through localized episodes of host-switching, presumably both into and out of the epinephelines. The Epinephelinae may well be typical of most groups of marine fishes both in the extent to which their trematode parasites are known and in that, apparently, co-evolution has contributed little to the evolution of their communities of trematodes.
Publisher: JSTOR
Date: 08-1998
DOI: 10.2307/3284590
Publisher: JSTOR
Date: 04-1995
DOI: 10.2307/3283931
Publisher: Springer Science and Business Media LLC
Date: 02-1998
Publisher: Informa UK Limited
Date: 12-1995
Publisher: JSTOR
Date: 12-1994
DOI: 10.2307/3283450
Publisher: Cambridge University Press (CUP)
Date: 07-2000
DOI: 10.1017/S0031182099006058
Abstract: Ecological factors may influence the number of parasites encountered and, thus, parasite species richness. These factors include diet, gregarity, conspecific and total host density, habitat, body size, vagility, and migration. One means of examining the influence of these factors on parasite species richness is through a comparative analysis of the parasites of different, but related, host species. In contrast to most comparative studies of parasite species richness of fish, which have been conducted by using data from the literature, the present study uses data obtained by the investigators. Coral reef fishes vary widely in the above ecological factors and are frequently parasitized by a erse array of parasites. We, therefore, chose to investigate how the above ecological factors influence parasite species richness in coral reef fishes. We investigated the endoparasite species richness of 21 species of butterfly fishes (Chaetodontidae) of New Caledonia. We mapped the diet characters on the existing butterfly fish phylogeny and found that omnivory appears to be ancestral. We also mapped the estimated endoparasite species richness, coded from low to high parasite species richness, on the existing butterfly fish phylogeny and found that low parasite species richness appears to be associated with the ancestral state of omnivory. Different dietary and social strategies appear to have evolved more than once, with the exception of obligate coralivory, which appears to have evolved only once. Finally, after controlling for phylogenetic relationships, we found that only the percentage of plankton in the diet and conspecific host density were positively correlated with endoparasite species richness.
Publisher: Springer Science and Business Media LLC
Date: 20-01-2016
DOI: 10.1007/S11230-015-9609-5
Abstract: Seven of the eleven species of Siganus Richardson (Siganidae) collected off the coasts of Australia, New Caledonia, French Polynesia and Palau were infected with species of Sclerocollum Schmidt & Paperna, 1978 (Acanthocephala: Cavisomidae). A Principal Component Analysis (PCA) and a Discriminant Analysis were performed on a morphometric dataset of specimens of Sclerocollum including borrowed type-specimens of Sc. rubrimaris Schmidt & Paperna, 1978 from the Indian Ocean and of Sc. robustum Edmonds, 1964, the only acanthocephalan species known previously from an Australian siganid. These analyses showed that the lengths of proboscis hooks were useful variables for separating specimens into groups and supported the presence of two known species (Sc. robustum and Sc. rubrimaris) and one new species (Sc. australis n. sp.) in Australian waters. We found Sc. robustum in Siganus lineatus (Valenciennes) from off Queensland and Sc. rubrimaris in S. fuscescens (Houttuyn) from off Western Australia and Queensland, S. punctatissimus Fowler & Bean from off Queensland and S. argenteus (Quoy & Gaimard), S. corallinus (Valenciennes), S. canaliculatus (Park) and S. doliatus Guérin-Méneville from off New Caledonia (all new host and locality records) which we compared with museum specimens of Sc. rubrimaris from S. rivulatus Forsskål & Niebuhr and S. argenteus [as S. rostratus (Valenciennes)] from the Red Sea. The third species, Sclerocollum australis n. sp., was found only in S. corallinus and S. doliatus from off Queensland. Sclerocollum australis n. sp. can be distinguished from its congeners by a unique combination of characters of the proboscis armature, including lengths of hooks 1-7. Specimens of Sclerocollum were also found in Zebrasoma velifer (Bloch) (Acanthuridae) from off Queensland, and Coradion altivelis McCulloch (Chaetodontidae) and Heniochus acuminatus (Linnaeus) (Chaetodontidae) from off New Caledonia. No acanthocephalans were found in siganids collected from Palau (Micronesia) or Moorea (French Polynesia) or Moreton Bay and Noosa (Queensland, Australia). We found no acanthocephalans in S. puellus (Schlegel), S. punctatus (Schneider & Forster), S. spinus (Linnaeus) or S. vulpinus (Schlegel & Müller). Evidence suggests that species of the genus Sclerocollum have travelled with S. argenteus across the Indo-Pacific with Sc. rubrimaris dispersed widely and Sc. robustum and Sc. australis n. sp. restricted to the Queensland coast, Australia.
Publisher: Elsevier BV
Date: 06-1991
Publisher: Springer Science and Business Media LLC
Date: 02-1991
DOI: 10.1007/BF00017660
No related grants have been discovered for Sylvie Pichelin.