Hostname: page-component-cd9895bd7-dzt6s Total loading time: 0 Render date: 2024-12-23T19:37:57.423Z Has data issue: false hasContentIssue false

Experimental study on the influence of paper and pulp mill effluent on the gill parasite communities of roach (Rutilus rutilus)

Published online by Cambridge University Press:  06 April 2009

A. M. Bagge
Affiliation:
University of jyväskylä, Department of Bio- and Environmental Science, PO Box 35, 40351 Jyväskylä, Finland
E. T. Valtonen*
Affiliation:
University of jyväskylä, Department of Bio- and Environmental Science, PO Box 35, 40351 Jyväskylä, Finland
*
* Corresponding author.

Summary

Roach (n = 81) caught on 23 May, 1992 from oligotrophic, unpolluted Lake Peurunka were kept in cages over a 2-week period before moving half of the fish to nearby Lake Vatia, which is influenced by pulp mill effluents. Before moving the fish gill parasites were examined from 9 fish; 5 Dactylogyrus species, Gyrodactylus sp. and Paradiplozoon homoion were found, the main components of the infracommunities being dactylogyrids. Afterwards, 5 fish from each lake were studied weekly between 1 July and 17 August. Metazoan parasites were recorded from gill arches divided into 4 sections along the dorso-ventral axis. D. crucifer, D. nanus, D. micracanthus and D. suecicus occurred in both lakes throughout the study. Gyrodactylus sp., Ergasilus briani and P. homoion occurred in low numbers in both lakes. Differences between the lakes were seen in the prevalence of D. micracanthus which was higher in Lake Vatia and significantly increased abundances of D. crucifer, D. nanus and D. micracanthus in Lake Vatia. Abundances of other Dactylogyrus species remained, on average, at the same level in both lakes. No change during the experiment was recorded in the location of the two most common species, D. crucifer and D. nanus, on the host gills in either of the lakes, both species favouring the 2nd and 3rd gill arches and especially the inner parts of the gills. The apparent lack of competition between the 2 most common Dactylogyrus species indicates that no limitation of resources on roach gills occurred. This was also confirmed by the increased overlapping indices with increasing abundances between the two most common species in Lake Vatia.

Type
Research Article
Copyright
Copyright © Cambridge University Press 1996

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

Arme, c. & Halton, D. w. (1972). Observations on the occurrence of Diclidophora merlangi (Trematoda: Monogenea) on the gills of whiting, Gadus merlangus. Journal of Fish Biology 4, 2732.CrossRefGoogle Scholar
Brown, J. H. (1975). Geographical ecology of desert rodents. In Ecology and Evolution of Communities (ed. Cody, M. L. & Diamond, J. M.), pp. 315341. Cambridge, Massachusetts: Belknap Press.Google Scholar
Cox, D. R. (1970). The Analysis of Binary Data. London: Methuen.Google Scholar
Dzika, E. & Szymanski, s. (1989). Co-occurrence and distribution of Monogenea of the genus Dactylogyrus on the gills of the bream, Abramis brama L. Acta Parasitologica Polonica 34, 114.Google Scholar
Granberg, K. E. (1992). Changes in water quality in Lake Päijänne following decrease of ef fluent load from the pulp and paper industry in 1969–1989. Hydrobiologia 234/244, 395403.CrossRefGoogle Scholar
Granberg, K., Palomäki, A., Hynynen, J., Meriläinen, J. & Salo, H. (1994). Limnological studies in the watercourse of Äänekoski in 1993. Reports of the Institute for Environmental Research, University of Jyväskylä. (In Finnish.)Google Scholar
Gusev, A. v. (1985). Keys to Parasites of Freshwater Fish of the U.S.S.R. Vol. 2. Parasitic Metazoa. Leningrad: Nauka. (In Russian.)Google Scholar
Hakkari, L. & Bagge, P. (1992). Reproductive success of Coregonus species in areas loaded by effluents from paper mills. Hydrobiologia 243/244, 405–12.CrossRefGoogle Scholar
Hanek, G. & Fernando, C. H. (1978). Spatial distribution of gill parasites of Lepomis gibbosus (L.) and Ambloplites rupestris (Raf.). Canadian Journal of Zoology 56, 1235–40.CrossRefGoogle Scholar
Höglund, J. & Thulin, J. (1989). Thermal effects on the seasonal dynamics of Paradiplozoon homoion (Bychowsky & Nagibina, 1959) parasiting roach, Rutilus rutilus (L.). Journal of Helminthology 63, 93101.CrossRefGoogle Scholar
Jokinen, E. I., Aaltonen, T. M. & Valtonen, E. T. (1995). Subchronic effects of pulp and paper mill effluents on the immunoglobulin synthesis of roach Rutilus rutilus. Aquatic Toxicology and Environmental Safety, (in the Press.)CrossRefGoogle ScholarPubMed
Kennedy, C. R., Bush, A. O. & Aho, J. M. (1986). Patterns in helminth communities: why are fish and birds different? Parasitology 93, 205–15.CrossRefGoogle ScholarPubMed
Koskivaara, M. & Valtonen, E. T. (1991). Paradiplozoon homoion (Monogenea) and some other gill parasites on roach Rutilus rutilus in Central Finland. Aqua Fennica 21, 137–43.Google Scholar
Koskivaara, M. & Valtonen, E. T. (1992). Dactylogyrus (Monogenea) communities on the gills of roach in three lakes in Central Finland. Parasitology 104, 263–72.CrossRefGoogle Scholar
Koskivaara, M., Valtonen, E. T. & Prost, M. (1991 a). Dactylogyrids on the gills of roach in Central Finland: features of infection and species composition. International Journal for Parasitology 21, 565–72.CrossRefGoogle ScholarPubMed
Koskivaara, M., Valtonen, E. T. & Prost, M. (1916). Seasonal occurrence of gyrodactylid monogeneans on the roach (Rutilus rutilus) and variations between four lakes of differing water quality in Finland. Aqua Fennica 21, 4755.Google Scholar
Koskivaara, M., Valtonen, E. T. & Vuori, K.-M. (1992). Microhabitat distribution and coexistence of Dactylogyrus species (Monogenea) on the gills of roach. Parasitology 104, 273–81.CrossRefGoogle Scholar
Krebs, J. c. (1989). Ecological Methodology. New York: Harper & Row.Google Scholar
Levins, R. (1968). Evolution in Changing Environments: Some Theoretical Explanations. Princeton, New Jersey: Princeton University Press.CrossRefGoogle Scholar
Pojmanska, T. & Dzika, E. (1987). Parasites of bream (Abramis brama L.) from the lake Goslawskie (Poland) affected by long-term thermal pollution. Acta Parasitologica Polonica 32, 139–61.Google Scholar
Rohde, K. (1979). A critical evaluation of intrinsinc and extrinsinc factors responsible for niche restriction in parasites. American Naturalist 114, 648–71.CrossRefGoogle Scholar
Rohde, K. (1991). Intra- and interspecific interactions in low density populations in resource-rich habitats. Oikos 60, 91104.CrossRefGoogle Scholar
Schoener, T. W. (1968). The Anolis lizards of Bimini: resource partitioning in a complex fauna. Ecology 49, 704–26.CrossRefGoogle Scholar
Soivio, A., Nikunen, E. & Tuurala, H. (1985). The toxicity of sodiumhypochlorite to fish in a watercourse polluted by paper and pulp mill effluents. Reports of Helsinki University, Zoological Department. (In Finnish.)Google Scholar
Stock, T. M. & Holmes, J. C. (1988). Functional relationships and microhabitat distributions of enteric helminths of grebes (Podicipedidae): the evidence for interactive communities. Journal of Parasitology 74, 214–27.CrossRefGoogle ScholarPubMed
Suydam, E. L. (1971). The micro-ecology of three species of monogenetic trematodes of fishes from the Beaufort-Cape Hatteras area. Proceedings of the Helminthological Society of Washington 38, 240–6.Google Scholar
Tuuha, H., Valtonen, E. T. & Taskinen, J. (1992). Ergasilid copepods as parasites of perch Perca fluviatilis and roach Rutilus rutilus in Central Finland: seasonality, maturity and environmental influence. Journal of Zoology 228, 405–22.CrossRefGoogle Scholar
Werner, E. E. (1986). Species interactions in freshwater fish communities. In Community Ecology (ed. Diamond, J. & Case, T. J.), pp. 344358. New York: Harper and Row.Google Scholar
Wilkinson, L. (1990). SYSTAT: The System for Statistics. Evanston, IL: Systat Inc.Google Scholar
Wootten, R. (1974). The spatial distribution of Dactylogyrus amphibothrium on the gills of ruffe Gymnocephalus cernua and its relation to the relative amounts of water passing over the parts of gills. Journal of Helminthology 48, 167–74.CrossRefGoogle Scholar
Zar, J. H. (1984). Biostatistical Analyzes. New Jersey, Englewood Cliffs: Prentice Hall.Google Scholar