Hostname: page-component-7479d7b7d-rvbq7 Total loading time: 0 Render date: 2024-07-12T06:45:38.437Z Has data issue: false hasContentIssue false
  • English
  • Français

Pomphorhynchus heronensis and restricted movement of Lutjanus carponotatus on the Great Barrier Reef

Published online by Cambridge University Press:  12 April 2024

T.H. Cribb ,
G.R. Anderson  and
A.D.M. Dove
T.H. Cribb*
Affiliation:
Department of Microbiology and Parasitology, The University of Queensland, Brisbane 4072, Australia
G.R. Anderson
Affiliation:
Department of Microbiology and Parasitology, The University of Queensland, Brisbane 4072, Australia
A.D.M. Dove
Affiliation:
Department of Microbiology and Parasitology, The University of Queensland, Brisbane 4072, Australia
*
*Fax: 61 7 3365 1588 E-mail: T.Cribb@mailbox.uq.edu.au
Get access Rights & Permissions [Opens in a new window]

Abstract

Samples of Lutjanus carponotatus(Lutjanidae) from reef flat (shallow) and reef slope (deep) sites around Heron and Wistari reefs on the southern Great Barrier Reef were examined for Pomphorhynchus heronensis(Acanthocephala). Individual fish from the reef slope had 0–9 (2.6) worms as compared with 1–122 (39.6) worms for individuals from the reef flat (P < 0.0001). Other variables (year, season, size of fish) made little contribution to the variation. Reef flat and reef slope sites were separated by as little as 300 m. These results imply both that the fish have very limited local movement and that transmission of the parasite is concentrated locally.

Type
Research Article
Information
Journal of Helminthology , Volume 74 , Issue 1 , March 2000 , pp. 53 - 56
Copyright
Copyright © Cambridge University Press 2000

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

Adlard, R.D. & Lester, R.J.G. (1994) Dynamics of the interaction between the parasitic isopod, Anilocra pomacentri, and the coral reef fish, Chromis nitida . Parasitology 109, 311–324.CrossRefGoogle ScholarPubMed
Barger, M.A. & Nickol, B.B. (1998) Structure of Leptorhynchoides thecatus and Pomphorhynchus bulbocolli (Acanthocephala) eggs in habitat partitioning and transmission. Journal of Parasitology 84, 534–537.CrossRefGoogle ScholarPubMed
Barrett, N.S. (1995) Short- and long-term movement patterns of six temperate reef fishes (families Labridae and Monacanthidae). Marine and Freshwater Research 46, 853–860.CrossRefGoogle Scholar
Bruce, N. (1993) Non-decapod Crustacea. pp. 97–107 in Mather, P. & Bennett, I. (Eds ) A coral reef handbook — a guide to the geology, flora and fauna of the Great Barrier Reef. Sydney, Surrey Beatty & Sons.Google Scholar
Choat, J.H. & Bellwood, D.R. (1985) Interactions among herbivorous fishes on a coral reef: Influence of spatial variation. Marine Biology (Berlin) 89, 221–234.CrossRefGoogle Scholar
Dezfuli, B.S., Zanini, N., Reggiani, G. & Rossi, R. (1991) Echinogammarus stammeri (Amphipoda) as an intermediate host for Pomphorhynchus laevis (Acanthocephala) parasite of fishes from the River Brenta. Bollettino di Zoologia 58, 167–171.CrossRefGoogle Scholar
Gleason, L.N. (1989) Movement of Pomphorhynchus bulbocolli larvae from the hemocoel to the peripheral circulation of Gammarus pseudolimnaeus . Journal of Parasitology 75, 982–985.CrossRefGoogle Scholar
Grutter, A.S. (1998) Habitat-related differences in the abundance of parasites from a coral reef fish: an indication of the movement patterns of Hemigymnus melapterus . Journal of Fish Biology 53, 49–57.Google Scholar
Hobson, E.S. (1965) Diurnal-nocturnal activity of some inshore fishes in the Gulf of California. Copeia 1965, 291–302.CrossRefGoogle Scholar
Leaman, B.M. & Kabata, Z. (1987) Neobrachiella robusta (Wilson, 1912) (Copepoda: Lernaeopodidae) as a tag for identification of stocks of its host, Sebastes alutus (Gilbert, 1890) (Pisces: Teleostei). Canadian Journal of Zoology 65, 2579–2582.CrossRefGoogle Scholar
Lester, R.J.G., Barnes, A. & Habib, G. (1985) Parasites of skipjack tuna, Katsuwonus pelamis: fishery implications. Fishery Bulletin 83, 343–356.Google Scholar
Lester, R.J.G., Sewell, K.B., Barnes, A. & Evans, K. (1988) Stock discrimination of orange roughy, Hoplostethus atlanticus, by parasite analysis. Marine Biology 99, 137–143.CrossRefGoogle Scholar
MacKenzie, K. (1990) Cestode parasites as biological tags for mackerel (Scomber scombrus L.) in the Northeast Atlantic. Journal du Conseil International pour l'Exploration de la Mer 46, 155–166.CrossRefGoogle Scholar
MacKenzie, K. (1993) Parasites as biological indicators. Bulletin of the Scandinavian Society for Parasitology 3, 1–10.Google Scholar
Pichelin, S. (1997) Pomphorhynchus heronensis sp. nov. (Acanthocephala: Pomphorhynchidae) from Lutjanus carponotatus (Lutjanidae) from Heron Island, Australia. Records of the South Australian Museum 30, 19–27.Google Scholar
Rigby, M.C., Holmes, J.C., Cribb, T.H. & Morand, S. (1997) Patterns of species diversity in the gastrointestinal helminths of a coral reef fish, Epinephelus merra (Serranidae), from French Polynesia and the South Pacific Ocean. Canadian Journal of Zoology 75, 1818–1827.CrossRefGoogle Scholar
Semenas, L., Ortubay, S. & Ubeda, C. (1992) Studies on the development and life history of Pomphorhynchus patagonicus Ortubay, Ubeda, Semenas et Kennedy, 1991 (Palaeacanthocephala). Research and Reviews in Parasitology 52, 3–4.Google Scholar
Sheaves, M.J. (1993) Patterns of movement of some fishes within an estuary in tropical Australia. Australian Journal of Marine and Freshwater Research 44, 867–880.CrossRefGoogle Scholar
Thresher, R.E. (1985) Distribution, abundance and reproductive success in the coral reef fish, Acanthochromis polyacanthus . Ecology 66, 1139–1150.CrossRefGoogle Scholar
Victor, B.C. (1987) The mating system of the Caribbean rosy razorfish, Xyrichtys martinicensis . Bulletin of Marine Science 40, 152–160.Google Scholar