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Impact of the cestode Triaenophorus nodulosus on the exotic Lepomis gibbosus and the autochthonous Perca fluviatilis

Published online by Cambridge University Press:  05 December 2014

G. MASSON ,
M. VANACKER ,
M. G. FOX  and
J.-N. BEISEL Open the ORCID record for J.-N. BEISEL [Opens in a new window]
G. MASSON
Affiliation:
Université de Lorraine, Laboratoire Interdisciplinaire des Environnements Continentaux (LIEC), CNRS UMR 7360, Campus Bridoux, Rue du Général Delestraint, F-57070 Metz, France
M. VANACKER
Affiliation:
Department of Agroecology and Environment, ISARA Lyon (member of university of Lyon), 23 rue Jean Baldassini, 69364 Lyon, France
M. G. FOX
Affiliation:
Environmental and Resource Studies Program and Department of Biology, Trent University, Peterborough, Ontario K9J 7B8, Canada
J.-N. BEISEL*
Affiliation:
Ecole Nationale du Génie de l'Eau et de l'Environnement de Strasbourg (ENGEES), 1 Quai Koch, BP 61039, 67070 Strasbourg, France Laboratoire Image, Ville, Environnement (LIVE), CNRS UMR 7362, Université de Strasbourg, 3 rue de l'Argonne, 67083 Strasbourg, France
*
* Corresponding author. Beisel J.-N., ENGEES, 1 quai Koch, 67000 Strasbourg, France. E-mail: jn.beisel@engees.unistra.fr
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Summary

The effects of plerocercoids of the cestode Triaenophorus nodulosus infecting the livers of native Eurasian perch Perca fluviatilis and non-native pumpkinseed Lepomis gibbosus was investigated in 17 sites along the Moselle watershed. With a single exception, infected individuals were not observed in the main channel whether or not northern pike Esox lucius, a final host, was present. In ponds where the pike was present, the prevalence of T. nodulosus averaged 86% in Eurasian perch and 15% in pumpkinseed. The parasite was not present at all in ponds when pike were absent. Parasite load, hepatosomatic index (HSI), gonadosomatic index (GSI) and body condition index (CI) were compared between hosts in one site where parasite prevalence and fish abundance was highest. HSI in infected perch was significantly higher than in uninfected perch, whereas no differences in HSI were detected between infected and uninfected pumpkinseed. While perch were more frequently infected and had a greater average parasite load than pumpkinseed, there were no significant differences in either indicator between the two species. Furthermore, no significant differences in GSI or CI were observed between infected and uninfected fish in either species, by either gender or maturity stage. We hypothesize that pumpkinseed is more resistant to the parasite or less likely to feed upon infected copepods than perch.

Keywords

liver parasiteinvasive speciescondition indiceswaterbodiesMoselle River
Type
Research Article
Information
Parasitology , Volume 142 , Issue 6 , May 2015 , pp. 745 - 755
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Copyright
Copyright © Cambridge University Press 2014 

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References

REFERENCES

Arme, C. (1968). Effects of the plerocercoids larva of a pseudophyllidean cestode, Ligula intestinalis, on the pituitary gland and gonads of its host. Biological Bulletin 134, 15–25.CrossRefGoogle Scholar
Balling, E. B. and Pfeiffer, W. (1997). Frequency distributions of fish parasites in the perch Perca fluviatilis L. from Lake Constance. Parasitology Research 83, 370–373.Google Scholar
Brinker, A. and Hamers, R. (2000). First description of pumpkinseed Lepomis gibbosus (L.) as a possible second intermediate host for Triaenophorus nodulosus (Pallas, 1781) (Cestoda, Pseudophyllidea) in Germany. Bulletin of the European Association of Fish Pathologists 2, 83.Google Scholar
Brinker, A. and Hamers, R. (2007). Evidence for negative impact of plerocercoid infection of Triaenophorus nodulosus on Perca fluviatilis L. stock in Upper Lake Constance, a water body undergoing rapid reoligotrophication. Journal of Fish Biology 71, 129–147.Google Scholar
Burnham, K. P. and Anderson, D. R. (2002). Model Selection and Multimodel Inference. Springer, New York.Google Scholar
Burns, J. R. (1976). The reproductive cycle and its environmental control in the pumpkinseed, Lepomis gibbosus (Pisces: Centrarchidae). Copeia 1976, 449–455.Google Scholar
Chubb, J. C. (1964). Observations on the occurrence of the plerocercoids of Triaenophorus nodulosus (Pallas, 1781) (Cestoda: Pseudophyllidea) in the perch Perca fluviatilis L. of Llyn Tegin (Bala Lake), Merionethshire. Parasitology 54, 481–491.CrossRefGoogle Scholar
Copp, G. H. and Fox, M. G. (2007). Growth and life history traits of introduced pumpkinseed (Lepomis gibbosus) in Europe, and the relevance to invasiveness potential. In Freshwater Bioinvaders: Profiles, Distribution, and Threats (ed. Gherardi, F.), pp. 289–306. Springer, Berlin.CrossRefGoogle Scholar
Copp, G. H., Fox, M. G., Przybylski, M., Godinho, F. N. and Vila-Gispert, A. (2004). Life-time growth patterns of pumpkinseed Lepomis gibbosus introduced to Europe, relative to native North American populations. Folia Zoologica 53, 237–254.Google Scholar
Craig, J. F. (1987). The Biology of Perch and Related Fish. Croom Helm, London, 333 pp.Google Scholar
Cucherousset, J. and Olden, J. D. (2011). Ecological impacts of nonnative freshwater fishes. Fisheries 36, 215–230.Google Scholar
Delahunty, G. and de Vlaming, V. L. (1980). Seasonal relationship of ovary weight, liver weight and fat stores with body weight in the goldfish, Carassius auratus (L.). Journal of Fish Biology 16, 5–13.CrossRefGoogle Scholar
Djikanović, V., Paunović, M., Nikolic, V., Simonović, P. and Cakić, P. (2012). Parasitofauna of freshwater fishes in the Serbian open waters: a checklist of parasites if freshwater fishes in Serbian open waters. Revue in Fish Biology and Fisheries 22, 297–234.Google Scholar
Fobert, E., Fox, M. G., Ridgway, M. and Copp, G. H. (2011). Heated competition: how climate change will affect non-native pumpkinseed Lepomis gibbosus and native perch Perca fluviatilis interactions in the U.K. Journal of Fish Biology 79, 1592–1607.CrossRefGoogle ScholarPubMed
Garnier, J., Billen, G. and Palfner, L. (1999). Understanding the oxygen budget of the Mosel drainage network with the concept of heterotrophic/autotrophic sequences: the Riverstrahler approach. Hydrobiologia 410, 151–166.Google Scholar
Hansen, J. M. and Leggett, W. C. (1985). Experimental and field evidence for inter- and intraspecific competition in two freshwater fishes. Canadian Journal of Fisheries and Aquatic Sciences 42, 280–286.Google Scholar
Hockley, F. A., Williams, C. F., Reading, A. J., Taylor, N. G. H. and Cable, J. (2011). Parasite fauna of introduced pumpkinseed fish Lepomis gibbosus: first British record of Onchocleidus dispar (Monogenea). Diseases of Aquatic Organisms 97, 65–73.Google Scholar
Hoffman, G. L. (1999). Parasites of North American Freshwater Fishes. Cornell University Press, 539 pp.Google Scholar
Izvekova, G. I. and Solovyev, M. M. (2012). The activity of digestive enzymes of the pike Esox lucius L. infected with the cestode Triaenophorus nodulosus (Pallas). Inland Water Biology 5, 113–118.CrossRefGoogle Scholar
Keast, A. (1978). Feeding interrelationships between age-groups of pumpkinseed (Lepomis gibbosus) and comparisons with bluegill (L. macrochirus). Journal of the Fisheries Research Board of Canada 35, 12–27.CrossRefGoogle Scholar
Košuthová, L., Koščo, J., Letková, V., Košuth, P. and Manko, P. (2009). New records of endoparasitic helminths in alien invasive fishes from the Carpathian region. Biologia 64, 776–780.CrossRefGoogle Scholar
Krone, O. (2007). Endoparasites. In Pathology. Raptor Research and Management Techniques, Vol. 17C, Hancock House, Surrey, British Columbia, Canada, 318–327.Google Scholar
Kuchta, R., Vlčková, R., Poddubnaya, L. G., Gustinelli, A., Dzika, E. and Scholz, T. (2007). Invalidity of three Palaearctic species of Triaenophorus tapeworms (Cestoda: Pseudophyllidea): evidence from morphometric analysis of scolex hooks. Folia Parasitologica 54, 34–42.CrossRefGoogle ScholarPubMed
Kuperman, B. I. (1973). Tapeworms of the Genus Triaenophorus, Parasites of Fishes. Amerind Publishing Co. Pvt. Ltd, New Delhi.Google Scholar
Kuperman, B. I. and Smirnova, L. I. (1970). Influence of Triaenophorus nodulosus Pallas) (Cestoda, Pseudophyllidea) on young perch of the current year. Fisheries Research Board of Canada 1470, 1–16.Google Scholar
Lahnsteiner, F., Kletzl, M. and Weismann, T. (2009). The risk of parasite transfer to juvenile fishes by live copepod food with the example Triaenophorus crassus and Triaenophorus nodulosus . Aquaculture 295, 120–125.CrossRefGoogle Scholar
Le Cren, E. D. (1951). The length-weight relationship and seasonal cycle in gonad weight and condition in the perch (Perca fluviatilis). Journal of Animal Ecology 2, 201–219.Google Scholar
Moore, J. (2002). Parasites and the Behaviour of Animals. Oxford University Press, Oxford.Google Scholar
Pascal, M., Lorvelec, O. and Vigne, J. D. (2006). Invasions Biologiques et Extinctions: 11 000 ans d'histoire des Vertébrés en France. Editions Belin-Quae, Paris, 350 pp.Google Scholar
Pasternak, A. F., Pulkkinen, K., Mikheev, V. N., Hasu, T. and Valtonen, E. T. (1999). Factors affecting abundance of Triaenophorus infection in Cyclops strenuous, and parasite-induced changes in host fitness. International Journal for Parasitology 29, 1793–1801.Google Scholar
Piasecki, W. and Falandysz, M. (1994). Preliminary survey on parasite fauna of pumpkinseed sunfish, Lepomis gibbosus (Linnaeus, 1758) (Pisces, Teleostei, Centrarchidae) from warm-water discharge canal of the ‘Pomorzany’ power plant in Szczecin, Poland. Acta Ichtyologica et Piscatoria 24, 87–100.CrossRefGoogle Scholar
Pilecka-Rapacz, M. and Sobecka, E. (2008). Parasitic nematodes of pumpkinseed sunfish (Lepomis gibbosus L., 1758) from warm-water canal of a power plant in Szczecin, Poland. Wiadomosci Parazytologiczne 54, 213–216.Google Scholar
Pulkkinen, K. and Valtonen, E. T. (1999). Accumulation of plerocercoids of Triaenophorus crassus in the second intermediate host Coregonus lavaretus and their effect on growth of the host. Journal of Fish Biology 55, 115–126.Google Scholar
Shaw, D. J., Grenfell, B. T. and Dobson, A. P. (1998). Patterns of macroparasite aggregation in wildlife host populations. Parasitology 117, 597–610.Google Scholar
Sterud, E. and Jorgensen, A. (2006). Pumpkinseed Lepomis gibbosus (Linnaeus, 1758) (Centrarchidae) and associated parasites introduced to Norway. Aquatic Invasions 4, 278–280.Google Scholar
Stromberg, P. C. and Crites, J. L. (1974). Triaenophoriasis in Lake Erie white bass, Morone chrysops . Journal of Wildlife Diseases, 10, 352–358.Google Scholar
Vanacker, M., Masson, G. and Beisel, J.-N. (2012). Host switch and infestation by Ligula intestinalis L. in a silver bream (Blicca bjoerkna L.) population. Parasitology 139, 406–417.Google Scholar
Vitule, J. R. S., Freire, C. A. and Simberloff, D. (2009). Introduction of non-native freshwater fish can certainly be bad. Fish Fisheries 10, 98–108.Google Scholar