Hostname: page-component-586b7cd67f-t7czq Total loading time: 0 Render date: 2024-11-23T05:02:50.277Z Has data issue: false hasContentIssue false
  • English
  • Français

Ectoparasites of the blackspot seabream Pagellus bogaraveo (Teleostei: Sparidae) from Portuguese waters of the north-east Atlantic

Published online by Cambridge University Press:  13 March 2012

Margarida Hermida ,
Cristina Cruz  and
Aurélia Saraiva
Margarida Hermida
Affiliation:
CIIMAR, Interdisciplinary Centre of Marine and Environmental Research, University of Porto, Rua dos Bragas, 289, 4050-123 Porto, Portugal
Cristina Cruz
Affiliation:
Faculdade de Ciências, Universidade do Porto, Departamento de Biologia, Rua do Campo Alegre, Edifício FC4, 4169-007 Porto, Portugal CIIMAR, Interdisciplinary Centre of Marine and Environmental Research, University of Porto, Rua dos Bragas, 289, 4050-123 Porto, Portugal
Aurélia Saraiva*
Affiliation:
Faculdade de Ciências, Universidade do Porto, Departamento de Biologia, Rua do Campo Alegre, Edifício FC4, 4169-007 Porto, Portugal CIIMAR, Interdisciplinary Centre of Marine and Environmental Research, University of Porto, Rua dos Bragas, 289, 4050-123 Porto, Portugal
*
Correspondence should be addressed to: A. Saraiva, Faculdade de Ciências, Universidade do Porto, Departamento de Biologia, Rua do Campo Alegre, Edifício FC4, 4169-007 Porto, Portugal email: [email protected]
Get access Rights & Permissions [Opens in a new window]

Abstract

The ectoparasite community of the blackspot seabream, Pagellus bogaraveo, was studied in different locations in Portuguese waters of the north-east Atlantic Ocean. This is the first study to focus on the ectoparasites of this commercially important sparid fish. Nine ectoparasite species were detected. Gnathia sp., Aega deshaysiana, A. antillensis, Rocinela danmoniensis and Argulus sp. are reported for the first time on this host. Significant differences were detected among the sampling locations, with monogeneans being more prevalent in mainland waters, and crustaceans being more prevalent in the Atlantic islands of Madeira and Azores. Fish from Madeira showed significantly higher infection levels of all ectoparasites, especially crustaceans, and particularly high prevalence of Hatschekia pagellibogneravei. The potential impact of the species detected on captive fish is also discussed, since the blackspot seabream is a promising new species for marine aquaculture.

Keywords

Pagellus bogaraveoblackspot seabreamPortugalnorth-east Atlanticectoparasites
Type
Research Article
Information
Journal of the Marine Biological Association of the United Kingdom , Volume 93 , Special Issue 2: Fish and Fisheries , March 2013 , pp. 503 - 510
Copyright
Copyright © Marine Biological Association of the United Kingdom 2012

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

REFERENCES

Alexander, P.D. (1983) Peniculus haemuloni, a new species of copepod (Siphonostomatoida: Pennelidae) parasitic on Haemulon stendachneri from Ubatuba, Brazil. Bulletin of the British Museum (Natural History), Zoology 45, 381–385.Google Scholar
Bariche, M. and Trilles, J.-P. (2008) Ceratothoa collaris (Isopoda: Cymothoidae) new to the eastern Mediterranean, with a redescription and comments on its distribution and host specificity. Journal of the Marine Biological Association of the United Kingdom 88, 85–93.Google Scholar
Basurco, B., Lovatelli, A. and García, B. (2011) Current status of Sparidae aquaculture. In Pavlidis, M.A. and Mylonas, C.C. (eds) Sparidae: biology and aquaculture of gilthead sea bream and other species. Oxford, UK: Blackwell Publishing, pp. 1–50.Google Scholar
Boualleg, C., Ferhati, H., Kaouachi, N., Bensouilah, M. and Ternengo, S. (2010a) The copepod parasite of the gills of four teleost fishes caught from the Gulf of Annaba (Algeria). African Journal of Microbiology Research 4, 801–807.Google Scholar
Boualleg, C., Seridi, M., Kaouachi, N., Quiliquini, Y. and Bensouillah, M. (2010b) Les Copépodes parasites de poissons téléostéens du littoral Est-algérien. Bulletin de l'Institut Scientifique, Rabat, section Sciences de la Vie 32, 65–72.Google Scholar
Boxshall, G.A. (1986) A new genus and two new species of Pennellidae (Copepoda: Siphonostomatoida) and an analysis of evolution within the family. Systematic Parasitology 8, 215–225.CrossRefGoogle Scholar
Bruce, N.L. (2004) Reassessment of the isopod crustacean Aega deshaysiana (Milne Edwards, 1840) (Cymothoidae: Aegidae): a world-wide complex of 21 species. Zoological Journal of the Linnean Society of London 142, 135–232.Google Scholar
Bunkley-Williams, L. and Williams, E.H. (1998) Isopods associated with fishes: a synopsis and corrections. Journal of Parasitology 84, 893–896.Google Scholar
Bush, A.O., Lafferty, K.D. and Shostak, A.W. (1997) Parasitology meets ecology on its own terms: Margolis et al. revisited. Journal of Parasitology 83, 575–583.Google Scholar
Carvalho, F. and Soares, A. (2001) A temperatura da água do mar em Portugal. Instituto de Meteorologia, Ministério da Ciência e Tecnologia, Nota Técnica VAM2-2/2001, 56 pp.Google Scholar
Davies, A.J., Eiras, J.C. and Austin, T.E. (1994) Investigations into the transmission of Haemogregarina bigemina Laveran & Mesnil, 1901 (Aplicomplexa: Adeleorina) between intertidal fishes in Portugal. Journal of Fish Diseases 17, 283–289.Google Scholar
Davies, A.J., Smit, N.J., Hayes, P.M., Seddon, A.M. and Wertheim, D. (2004) Haemogregarina bigemina (Protozoa: Aplicomplexa: Adeleorina)—past, present and future. Folia Parasitologica 51, 99–108.Google Scholar
Dawes, B. (1947) The Trematoda of British fishes. London: The Ray Society.Google Scholar
Desdevises, Y. (2006) Determinants of parasite species richness on small taxonomical and geographical scales: Lamellodiscus monogeneans of northwestern Mediterranean sparid fish. Journal of Helminthology 80, 235–241.Google ScholarPubMed
Desdevises, Y., Jovelin, R., Jousson, O. and Morand, S. (2000) Comparison of ribosomal DNA sequences of Lamellodiscus spp. (Monogenea, Diplectanidae) parasitising Pagellus (Sparidae, Teleostei) in the North Mediterranean Sea: species divergence and coevolutionary interactions. International Journal for Parasitology 30, 741–746.Google Scholar
Gene, E. (2007) Infestation status of gnathiid isopod juveniles parasitic on dusky grouper (Epinephelus marginatus) from the northeast Mediterranean Sea. Parasitology Research 101, 761–766.Google Scholar
González, P., Sánchez, M.I., Chirivella, J., Carbonell, E., Riera, F. and Grau, A. (2004) A preliminary study on gill metazoan parasites of Dentex dentex (Pisces: Sparidae) from the western Mediterranean Sea (Balearic Islands). Journal of Applied Ichthyology 20, 276–281.Google Scholar
Gooding, R.U. (1957) On some copepoda from Plymouth, mainly associated with invertebrates, including three new species. Journal of the Marine Biological Association of the United Kingdom 36, 195–221.Google Scholar
Grutter, A.S. (2003) Feeding ecology of the fish ectoparasite Gnathia sp. (Crustacea: Isopoda) from the Great Barrier Reef, and its implications for fish cleaning behaviour. Marine Ecology Progress Series 259, 295–302.CrossRefGoogle Scholar
Hadfield, K.A., Smit, N.J. and Avenant-Oldewage, A. (2009) Life cycle of the temporary fish parasite, Gnathia pilosus (Crustacea: Isopoda: Gnathiidae) from the east coast of South Africa. Journal of the Marine Biological Association of the United Kingdom 89, 1331–1339.Google Scholar
Hakalahti, T., Karvonen, A. and Valtonen, E.T. (2006) Climate warming and disease risks in temperate regions—Argulus coregoni and Diplostomum spathaceum as case studies. Journal of Helminthology 80, 93–98.Google Scholar
Hansson, H.G. (1998) NEAT (North East Atlantic Taxa): South Scandinavian Marine Plathelminthes Check-List. Available from http://www.tmbl.gu.se/libdb/taxon/neat_pdf/ NEAT*Plathelmint.pdf (accessed 30 November 2011).Google Scholar
Heupel, M.R. and Bennett, M.B. (1999) The occurrence, distribution and pathology associated with gnathiid isopod larvae infecting the epaulette shark, Hemiscyllium oscellatum . International Journal for Parasitology 29, 321–330.Google Scholar
Jones, C.M. and Grutter, A.S. (2005) Parasitic isopods (Gnathia sp.) reduce haematocrit in captive blackeye thicklip (Labridae) on the Great Barrier Reef. Journal of Fish Biology 66, 860–864.Google Scholar
Jones, J.B. (1985) A revision of Hatschekia Poche, 1902 (Copepoda: Hatschekiidae), parasitic on marine fishes. New Zealand Journal of Zoology 12, 213–271.CrossRefGoogle Scholar
Kabata, Z. (1979) Parasitic Copepoda of British fishes. London: The Ray Society.Google Scholar
Kabata, Z. (1992) Copepods parasitic on fishes: keys and notes for the identification of the species. Oegstgeest , The Netherlands, The Linnean Society of London and The Estuarine and Coastal Sciences Association [Synopses of the British Fauna (New Series), No. 47.]Google Scholar
Kaouachi, N., Boualleg, C., Bensouilah, M. and Marchand, B. (2010) Monogenean parasites in sparid fish (Pagellus genus) in eastern Algeria coastline. African Journal of Microbiology Research 4, 989–993.Google Scholar
Kearn, G.C. (2005) Leeches, lice and lampreys: a natural history of skin and gill parasites of fishes. Dordrecht , The Netherlands: Springer.Google Scholar
Llewellyn, J. (1941) A description of the anatomy of the monogenetic trematode Choricotyle chrysophryi van Beneden & Hesse. Parasitology 33, 397–405.Google Scholar
Llewellyn, J. (1956) The host-specificity, micro-ecology, adhesive attitudes, and comparative morphology of some trematode gill parasites. Journal of the Marine Biological Association of the United Kingdom 35, 113–127.Google Scholar
Marino, F., Giannetto, S., Paradiso, M.L., Bottari, T., De Vico, G. and Macrì, B. (2004) Tissue damage and haematophagia due to praniza larvae (Isopoda: Gnathiidae) in some aquarium seawater teleosts. Diseases of Aquatic Organisms 59, 43–47.Google Scholar
Marques, J.F., Teixeira, C.M. and Cabral, H.N. (2006) Differentiation of commercially important flatfish populations along the Portuguese coast: evidence from morphology and parasitology. Fisheries Research 81, 293–305.CrossRefGoogle Scholar
Norman, A.M. and Scott, T. (1906) The Crustacea of Devon and Cornwall. London: William Wesley & Son.CrossRefGoogle Scholar
Novotny, A.J. and Mahnken, C.V.W. (1971) Predation on juvenile Pacific salmon by a marine isopod Rocinela belliceps pugettensis (Crustacea: Isopoda). Fishery Bulletin 69, 699–701.Google Scholar
Oliver, G. (1973) Lamellodiscus obeliae n. sp., une nouvelle espèce de diplectanidae (Monogenea, Monopisthocotylea) parasite de Pagellus centrodontus (Delaroche, 1809) (Pisces, Sparidae). Zeitschrift für Parasitenkunde 41, 103–108.Google Scholar
Peleteiro, J.B., Olmedo, M. and Alvarez-Blázquez, B. (2000) Culture of Pagellus bogaraveo: present knowledge, problems and perspectives. Cahiers Options Méditerranéennes 47, 141–151.Google Scholar
Pérez-del-Olmo, A., Raga, J.A., Kostadinova, A. and Fernández, M. (2007) Parasite communities in Boops boops (L.) (Sparidae) after the Prestige oil-spill: detectable alterations. Marine Pollution Bulletin 54, 266–276.Google Scholar
Raibaut, A., Combes, C. and Benoit, F. (1998) Analysis of the parasitic copepod species richness among Mediterranean fish. Journal of Marine Systems 15, 185–206.Google Scholar
Ramdane, Z. and Trilles, J.-P. (2008) Cymothoidae and Aegidae (Crustacea, Isopoda) from Algeria. Acta Parasitologica 53, 173–178.Google Scholar
Richardson, H. (1905) Monograph on the isopods of North America. Bulletin of the United States National Museum 54, 1–727.Google Scholar
Rohde, K., Hayward, C. and Heap, M. (1995) Aspects of the ecology of metazoan ectoparasites of marine fishes. International Journal for Parasitology 25, 945–970.Google Scholar
Rohde, K. and Heap, M. (1998) Latitudinal differences in species and community richness and in community structure of metazoan endo- and ectoparasites of marine teleost fish. International Journal for Parasitology 28, 461–474.Google Scholar
Rokicki, J. (1985) Biology of adult Isopoda (Crustacea) parasitizing fishes of the North-West Africa shelf. Acta Ichthyologica et Piscatoria 15, 95–118.Google Scholar
Sánchez-García, N., Padrós, F., Raga, J.A. and Montero, F.E. (2011) Comparative study of the three attachment mechanisms of diplectanid monogeneans. Aquaculture 318, 290–299.Google Scholar
Sars, G.O. (1899) An account of the Crustacea of Norway, with short descriptions and figures of all the species. Volume 2. Isopoda. Bergen, Norway: The Bergen Museum.Google Scholar
Schram, T.A., Iversen, L., Heuch, P.A. and Sterud, E. (2005) Argulus sp. (Crustacea: Branchiura) on cod, Gadus morhua from Finnmark, northern Norway. Journal of the Marine Biological Association of the United Kingdom 85, 81–86.Google Scholar
Scott, T. and Scott, A. (1913) The British parasitic Copepoda. Volume I. Copepoda parasitic on fishes. London: The Ray Society.Google Scholar
Sequeira, V., Gordo, L.S., Neves, A., Paiva, R.B., Cabral, H.N. and Marques, J.F. (2010) Macroparasites as biological tags for stock identification of the bluemouth, Helicolenus dactylopterus (Delaroche, 1809) in Portuguese waters. Fisheries Research 106, 321–328.Google Scholar
Ternengo, S., Levron, C., Mouillot, D. and Marchand, B. (2009) Site influence in parasite distribution from fishes of the Bonifacio Strait Marine Reserve (Corsica Island, Mediterranean Sea). Parasitology Research 104, 1279–1287.CrossRefGoogle ScholarPubMed