Skip to main content
Log in

Changes in aquatic plant communitieson the island of Valaam due to invasion by the muskrat Ondatra zibethicus L.(Rodentia, Mammalia)

  • Published:
Biodiversity & Conservation Aims and scope Submit manuscript

Abstract

Muskrat invaded Valaam Island (Northern part of European Russia) in the 1970s. Aquatic plant communities of 1962 and 1993 were compared on the same plots. Quantitative changes were tested with the help of jack-knifing estimates of most known inventory (α-) diversity indicators. Qualitative transformations were assessed using β-diversity values. The results demonstrated substantially more discriminant ability of diversity measures than classical methods of mathematical statistics. All of the α-diversity values declined synchronously without exception. Species composition also changed greatly and those species which turn out to be more resistant to muskrat grazing became the main dominant plants. The activity of Ondatra became the over-riding ecological factor connecting the littoral plant communities of the Valaam. It is concluded that the sustainability of this ecosystem was damaged by muskrat's invasion and that the role of muskrat should not be underestimated when studying the ecology of freshwater littoral communities.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  • (1962-1993) Vodniy kadastr (Annual data on regime and resources of the internal water bodies of Russia) part 1-2, Vol.1, Iss.5. Leningrad.

  • (1982) Anthropogenous eutrophication of the Ladoga lake. Leningrad: Nauka.

  • (1987 Modern state of the Ladozhskoye Lake ecosystem. Leningrad: Nauke.

  • (1993) The muskrat: Morphology, Systematics, Ecology. Moscow: Nauka.

  • Abramsky, Z. and Rosenzweig, M.L. (1984) Tilman’s predicted productivity-diversity relationship shown by desert rodents. Nature 309, 150–1.

    Google Scholar 

  • Armstrong, J. and Armstrong, W. (1988) Phragmites australis — a preliminary study of soil-oxidising sites and internal gas transport pathways. New Phytol. 108, 373–82.

    Google Scholar 

  • Armstrong, J. and Armstrong, W. (1990) Light enhanced convective throughflow increases oxygenation in rhizomes and rhizosphere of Phragmites australis (Cav.) Trin. ex Steud. New Phytol. 114, 121–8.

    Google Scholar 

  • Armstrong, J. and Armstrong, W. (1991) A convective through-flow of gases in Phragmites australis (Cav.) Trin, ex Steud. Aquat. Bot. 39, 75–88.

    Google Scholar 

  • Armstrong, W. and Beckett, P. M. (1987) Internal aeration and the development of stellar anoxia in submerged roots. A multishelled mathematical model combining axial diffusion of oxygen in the cortex with radial oxygen losses to the stele, the wall layers and the rhizosphere. New Phytol. 105, 221–45.

    Google Scholar 

  • Armstrong, W., Armstrong, J. and Beckett, P. M. (1990) Measurement and modelling of oxygen release from roots of Phragmites australis. In Constructed Wetlands is Water Pollution Control (P. F. Cooper and C. Findlater, eds) pp. 41–52. Oxford: Pergamon Press.

    Google Scholar 

  • Artimo, A. (1960) The dispersal and acclimatization of the muskrat, Ondatra zibethicus (L.), in Finland. Riistat. Julk. 21, 1–101.

    Google Scholar 

  • Barclay, A. M. and Crawford, R. M. M. (1982) Plant growth and survival under strict anaerobiosis. J. Exp. Bot. 134, 541–9.

    Google Scholar 

  • Berger, W. H. and Parker, F. L. (1970) Diversity of planktonic Foraminifera in deep sea sediments. Science 168, 1345–7.

    Google Scholar 

  • Chaschukhin, V. A. (1975) Impact of ondatra on aquatic vegetation. Bull. MOIP, biol. (Bulletin of the Moscow Society of Nature Users, dept. Biolog. (Russia) 80,(6) 21–9.

    Google Scholar 

  • Chaschukhin, V. A. (1987) Selective foraging water macrophytes by muskrat. Ekologiya (Russia) 6, 78–80.

    Google Scholar 

  • Chaschukhin, V. A. (1990) Muskrat, Remarkable Result of Acclimatisation. Kirov: Tzentrosoyoz SSSR.

    Google Scholar 

  • Cizkova-Koncalova, H., Kvet, J. and Thompson, K. (1992) Carbon starvation: a key to reed decline in eutrophic lakes. Aquat. Bot. 43, 105–13.

    Google Scholar 

  • Clifford, H. T. and Stephenson, W. (1975) An Introduction to Numerical Classification. London: Academic Press.

    Google Scholar 

  • Danell, K. (1977) Short-term plant succession following the colonization of northern Swedish lake by the muskrat, Ondatra zibethica. J. Appl. Ecol. 14, 933–47.

    Google Scholar 

  • Danell, K. (1978) Intra-and interannual changes in habitat selection by the muskrat. J. Wildl. Manag. 42, 540–9.

    Google Scholar 

  • Danell, K. (1979) Reduction of aquatic vegetation following the colonization of northern Swedish lake by the muskrat, Ondatra zibethica (L.). Oecol. 38, 101–6.

    Google Scholar 

  • Den Hartog, C., Kvet, J. and Sukopp, H. (1989) Reed. A common species in decline. Aquat. Bot. 35, 1–4.

    Google Scholar 

  • Errington, P. Z. (1963) Muskrat Populations. Iowa: Iowa State University Press.

    Google Scholar 

  • Farmer, A. M. (1990) The effect of lake acidification on aquatic macrophytes — a review. Environ. Pollut. 65, 219–40.

    Google Scholar 

  • Fisher, R. A., Corbet, A. S. and Williams, C. B. (1943) The relation between the number of species and the number of individuals in a sample of an animal population. J. Anim. Ecol. 12, 42–58.

    Google Scholar 

  • Gacia, E., Ballesteros, E., Camarero, L. et al. (1994) Macrophytes from lakes in the Eastern Pyrenees: community composition and ordination in relation to environmental factors. Freshwater Biol. 32, 73–81.

    Google Scholar 

  • Helings, S. E. and Gallagher, J. L. (1992) The effect of salinity and flooding on Phragmites australis. J. Appl. Ecol. 29, 41–9.

    Google Scholar 

  • Koryakin, A. N. (1978) Littoral vegetation in water bodies of the Solovetskiye Islands before Ondatra introduction (1928) and at present time. Trudy Kirovskogo s.-kh. in-ta Proc. S. M. Kirov Inst. Agric. 58, 43–51.

    Google Scholar 

  • Krasovsky, L. I. (1962) Daily requirement of muskrat in natural feed. Zool. Zhur. 41, 1529–35.

    Google Scholar 

  • Lavrov, N. P. (1960) Selection from ‘Acclimatization of muskrats in the USSR’. Translations of Russian Game Reports 7:1-150. Ottawa: Canadian Wildlife Service.

    Google Scholar 

  • Macarthur, R. A. (1957) On the relative abundance of bird species. Proc. Natl. Acad. Sci. USA 43, 293–5.

    Google Scholar 

  • Magurran, A. E. (1981) Biological Diversity and Woodland Management. Unpublished D. Phil. thesis, New University of Ulster.

  • Magurran, A. E. (1988) Ecological Diversity and its Measurement. London: Croom Helm.

    Google Scholar 

  • Marcstrøm, V. (1964) The muskrat Ondatra zibethicus (L.) in Northern Sweden. Viltrevy 2, 329–407.

    Google Scholar 

  • Molinari, J. (1989) A calibrated index for the measurement of evenness. Oikos 56, 319–26.

    Google Scholar 

  • Motomura, I. (1932) A statistical treatment of associations. Jpn. J. Zool. 44, 379–83.

    Google Scholar 

  • Nasimovich, A. A. (1966) Ecological consequences of introducing new species in terrestrial biocenosis (Muskrat in Eurasia). Zool. Zhur. 45, 1593–9.

    Google Scholar 

  • Nyman, J. A., Chabreck, R. H. and Kinler, N. W. (1993) Some effects of herbivory and 30 years of weir management on emergent vegetation in brackish marsh. Wetlands 13, 165–75.

    Google Scholar 

  • O’Neil, T. (1949) The Muskrat in the Louisiana Coastal Marshes. New Orleans: Louisiana Department of Wildlife and Fisheries.

  • Ostendorp, W. (1989) ‘Die-back’ of reeds in Europe — a critical review of literature. Aquat. Bot. 35, 5–26.

    Google Scholar 

  • Pelican, J., Svoboda, J. and Kvet, J. (1970) On some relations between the production of Typha latifolia and a muskrat population. Zool. Listy, 19, 303–20.

    Google Scholar 

  • Pielou, E. C. (1969) An Introduction to Mathematical Ecology. New York: Wiley.

    Google Scholar 

  • Pielou, E. C. (1975) Ecological Diversity. New York: Wiley.

    Google Scholar 

  • Platt, H. M., Shaw, K. M. and Lambshead, P. J. D. (1984) Nematode species abundance patterns and their use in the detection of environmental perturbations. Hydrobiologia 118, 59–66.

    Google Scholar 

  • Preston, F. W. (1948) The commonness and rarity of species. Ecology 294, 254–83.

    Google Scholar 

  • Quenouille, M. H. (1956) Notes on bias in estimation. Biometrika 43, 353–60.

    Google Scholar 

  • Rorslett, B. (1991) Principal determinants of aquatic macrophyte richness in northern European lakes. Aquat. Bot. 39, 173–93.

    Google Scholar 

  • Rosenzweig, M. L. (1992) Species diversity gradients: we know more and less that we thought. J. Mammal. 73, 715–30.

    Google Scholar 

  • Simpson, E. H. (1949) Measurement of diversity. Nature 163, 688–8.

    Google Scholar 

  • Smirnov, V. V. and Shvarts, E. A. (1995) Ecosystem consequences of Ondatra acclimatization in Eurasia. Setting up the problem. In Ecosistemy Severa (Ecosystems of the North): Structure, adaptations, stability (I. A. Shilov, ed.) pp. 243–56. Moscow: Russian Academy Press.

    Google Scholar 

  • Southwood, T. R. E. (1978) Ecological Methods. London: Chapman and Hall.

    Google Scholar 

  • Tilman, D. (1982) Resource Competition and Community Structure. Princeton University Press.

  • Tukey, J. (1958) Bias and confidence in not quite large samples. Ann. Math. Stat. 29, 614.

    Google Scholar 

  • Weisner, S. E. B. and Graneli, W. (1989) Influence of substrate conditions on the growth of Phragmites australis after a reduction in oxygen transport to below ground parts. Aquat. Bot. 35, 71–80.

    Google Scholar 

  • Whittaker, R. H. (1977) Evolution of species diversity in land communities. In Evolutionary Biology, Vol. 10 (M. K. Hecht, W. C. Steere and B. Wallace, eds) pp. 1–67. New York: Plenum.

    Google Scholar 

  • Willner, G. R., Feldhamer, G. A., Zucker, E. E. and Chapman, I. A. (1980) Ondatra zibethicus. Mammal. Spec. 141, 1–8.

    Google Scholar 

  • Janson, S. and Vegelius, J. (1981) Measures of ecological association. Oecol. 49, 371–6.

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Smirnov, V.V., Tretyakov, K. Changes in aquatic plant communitieson the island of Valaam due to invasion by the muskrat Ondatra zibethicus L.(Rodentia, Mammalia). Biodiversity and Conservation 7, 673–690 (1998). https://doi.org/10.1023/A:1008860603166

Download citation

  • Issue Date:

  • DOI: https://doi.org/10.1023/A:1008860603166

Navigation