Oecologia

, Volume 151, Issue 1, pp 104–114 | Cite as

Long-term response of Dreissena polymorpha larvae to physical and biological forcing in a shallow lake

Global Change and Conservation Ecology

Abstract

Müggelsee, a shallow eutrophic lake (Berlin, Germany), has been subject to global warming and concurrent reductions of anthropogenic nutrient loading during the past decades. Here, we focus on the recent increase in abundance of Dreissena polymorpha larvae. We aimed at ascertaining whether the change in abundance of larvae was driven by changes in climate, especially by climate warming, and/or by the concurrent changes in trophic state of the lake. Both the numbers of small, newly developed larvae and their lengths have increased in recent years, suggesting that conditions for overall reproductive success have improved. The timing of the increase in abundance of larvae was matched by changes in nutrient loading and phytoplankton biomass, induced by a reduced inflow of nutrients into the lake. Besides a correlation between the first appearance of larvae each year and the timing of the requisite temperature for first spawning (12°C), no relationship between changes in water temperature and abundance, length and survival rates of larvae was found. However, a sudden drop in abundance of larvae in 2003 may be primarily attributed to low dissolved oxygen conditions during an unusually long period of stratification, induced by anomalous meteorological conditions. The increase in length and survival rates of larvae was most likely due to changes in food composition, which followed the decrease in nutrient availability, and to changes in the occurrence of planktivorous fish. The results suggest that the first appearance of larvae per year and the decline in abundance of larvae in 2003 were driven by climatic influences, while the overall increase in abundance and length of D. polymorpha larvae in Müggelsee was more likely caused by changes in the trophic state of the lake rather than by climate warming.

Keywords

Zebra mussel Veliger Size–frequency distribution Trophic state Climate warming 

Notes

Acknowledgements

We thank the staff of the Leibniz Institute of Freshwater Ecology and Inland Fisheries involved in the long-term monitoring at Müggelsee. We also thank R. Rusche and U. Newen for a preliminary investigation on larval length. The study benefited from the helpful comments of I.G. Boëchat, G.L. Mackie, A. Schwalb and N. Walz. We very much appreciated suggestions made by two anonymous reviewers, which improved the quality of the manuscript substantially. Funding was provided by the European Union within the framework of the project CLIME (Climate and lake impacts in Europe; contract no. EVK1-CT-2002-00121) and by Deutsche Forschungsgemeinschaft (DFG) within the priority program “AQUASHIFT” (Ad91/12-1).

References

  1. Ackerman JD, Sim B, Nichols SJ, Claudi R (1994) Review of the early life history of zebra mussels (Dreissena polymorpha): comparisons with marine bivalves. Can J Zool 72:1169–1179Google Scholar
  2. Adrian R, Wilhelm S, Gerten D (2006) Life-history traits of lake plankton species may govern their phenological response to climate warming. Global Change Biol 12:1–10. DOI 10.1111/j.1365-2486.2006.01125.xCrossRefGoogle Scholar
  3. Anderson NJ, Jeppesen E, Sondergaard M (2005) Ecological effects of reduced nutrient loading (oligotrophication) on lakes: an introduction. Freshw Biol 50:1589–1593CrossRefGoogle Scholar
  4. Anneville O, Ginot V, Druart JC, Angeli N (2002) Long-term study (1974–1998) of seasonal changes in the phytoplankton in Lake Geneva: a multi-table approach. J Plankton Res 24:993–1007CrossRefGoogle Scholar
  5. Anneville O, Gammeter S, Straile D (2005) Phosphorus decrease and climate variability: mediators of synchrony in phytoplankton changes among European peri-alpine lakes. Freshw Biol 50:1731–1746CrossRefGoogle Scholar
  6. Borcherding J (1991) The annual reproductive cycle of the freshwater mussel Dreissena polymorpha Pallas in lakes. Oecologia 87:208–218CrossRefGoogle Scholar
  7. Borcherding J (1995) Laboratory experiments on the influence of food availability, temperature and photoperiod on gonad development in the freshwater mussel Dreissena polymorpha. Malacologia 36:15–27Google Scholar
  8. Burla H, Ribi G (1998) Density variation of the zebra mussel Dreissena polymorpha in Lake Zürich, from 1976 to 1988. Aquat Sci 60:145–156Google Scholar
  9. Driescher E, Behrendt H, Schellenberger G, Stellmacher R (1993) Lake Müggelsee and its environment—natural conditions and anthropogenic impacts. Internationale Revue der gesamten Hydrobiologie 78:327–343CrossRefGoogle Scholar
  10. Edmondson WT, Abella SEB, Lehman JT (2003) Phytoplankton in Lake Washington: long-term changes 1950–1999. Arch Hydrobiol Suppl 139:275–326Google Scholar
  11. Gerten D, Adrian R (2000) Climate-driven changes in spring plankton dynamics and the sensitivity of shallow polymictic lakes to the North Atlantic Oscillation. Limnol Oceanogr 45:1058–1066CrossRefGoogle Scholar
  12. Gerten D, Adrian R (2002a) Effects of climate warming, North Atlantic Oscillation, and El Nino–Southern Oscillation on thermal conditions and plankton dynamics in northern hemispheric lakes. ScientificWorldJournal 2:586–606CrossRefGoogle Scholar
  13. Gerten D, Adrian R (2002b) Species-specific changes in the phenology and peak abundance of freshwater copepods in response to warm summers. Freshw Biol 47:2163–2173CrossRefGoogle Scholar
  14. Hays GC, Richardson AJ, Robinson C (2005) Climate change and marine plankton. Trends Ecol Evol 20:337–344PubMedCrossRefGoogle Scholar
  15. Hebert PDN, Muncaster BW, Mackie GL (1989) Ecological and genetic studies on Dreissena polymorpha (Pallas): a new mollusc in the Great Lakes. Can J Fish Aquat Sci 46:1587–1591Google Scholar
  16. Jeppesen E, Sondergaard M, Jensen JP, Havens KE, Anneville O, Carvalho L, Coveney MF, Deneke R, Dokulil MT, Foy B, Gerdeaux D, Hampton SE, Hilt S, Kangur K, Köhler J, Lammens EHHR, Lauridsen TL, Manca M, Miracle MR, Moss B, Noges P, Persson G, Phillips G, Portielje R, Schelske CL, Straile D, Tatrai I, Willen E, Winder M (2005) Lake responses to reduced nutrient loading—an analysis of contemporary long-term data from 35 case studies. Freshw Biol 50:1747–1771CrossRefGoogle Scholar
  17. Johnson PD, McMahon RF (1998) Effects of temperature and chronic hypoxia on survivorship of the zebra mussel (Dreissena polymorpha) and Asian clam (Corbicula fluminea). Can J Fish Aquat Sci 55:1564–1572CrossRefGoogle Scholar
  18. Kinzelbach R (1995) Neozoans in European waters—exemplifying the worldwide process of invasion and species mixing. Experientia 51:526–538CrossRefGoogle Scholar
  19. Köhler J, Hilt S, Adrian R, Nicklisch A, Kozerski HP, Walz N (2005) Long-term response of a shallow, moderately flushed lake to reduced external phosphorus and nitrogen loading. Freshw Biol 50:1639–1650CrossRefGoogle Scholar
  20. Liebig JR, Vanderploeg HA (1995) Vulnerability of Dreissena polymorpha larvae to predation by Great-Lakes calanoid copepods—the importance of the bivalve shell. J Great Lakes Res 21:353–358Google Scholar
  21. MacIsaac HJ, Sprules WG, Leach JH (1991) Ingestion of small-bodied zooplankton by zebra mussels (Dreissena polymorpha)—can cannibalism on larvae influence population dynamics. Can J Fish Aquat Sci 48:2051–2060CrossRefGoogle Scholar
  22. Marcus N (2004) An overview of the impacts of eutrophication and chemical pollutants on copepods of the coastal zone. Zool Stud 43:211–217Google Scholar
  23. Mills EL, Ogorman R, Roseman EF, Adams C, Owens RW (1995) Planktivory by alewife (Alosa pseudoharengus) and rainbow smelt (Osmerus mordax) on microcrustacean zooplankton and dreissenid (Bivalvia, Dreissenidae) veligers in southern Lake Ontario. Can J Fish Aquat Sci 52:925–935Google Scholar
  24. Molloy DP, Karatayev AY, Burlakowa LE, Kurandina DP, Laruelle F (1997) Natural enemies of zebra mussels: predators, parasites, and ecological competitors. Rev Fish Sci 5:27–97CrossRefGoogle Scholar
  25. Nalepa TF, Schloesser DW (1992) Zebra mussels: biology, impacts, and control. Lewis, Boca RatonGoogle Scholar
  26. Neumann D, Borcherding J, Jantz B (1993) Growth and seasonal reproduction of Dreissena polymorpha in the River Rhine and adjacent waters. In: Nalepa TF, Schloesser DW (eds) Zebra mussels: biology, impacts, and control. Lewis, Boca Raton, pp. 95–109Google Scholar
  27. Nichols SJ (1996) Variations in the reproductive cycle of Dreissena polymorpha in Europe, Russia, and North America. Am Zool 36:311–325Google Scholar
  28. Oderbrecht W (1957) Ausbreitung der Wander- oder Zebramuschel in Europa. Urania Monatschrift über Natur und Gesellschaft 20:24–27Google Scholar
  29. Page ES (1955) A test for a change in a parameter occurring at an unknown point. Biometrika 42:523–527Google Scholar
  30. Pires LMD, Jonker RR, Van Donk E, Laanbroek HJ (2004) Selective grazing by adults and larvae of the zebra mussel (Dreissena polymorpha): application of flow cytometry to natural seston. Freshw Biol 49:116–126CrossRefGoogle Scholar
  31. Schär C, Vidale PL, Luthi D, Frei C, Haberli C, Liniger MA, Appenzeller C (2004) The role of increasing temperature variability in European summer heatwaves. Nature 427:332–336PubMedCrossRefGoogle Scholar
  32. Schneider DW, Madon SP, Stoeckel JA, Sparks RE (1998) Seston quality controls zebra mussel (Dreissena polymorpha) energetics in turbid rivers. Oecologia 117:331–341CrossRefGoogle Scholar
  33. Schneider DW, Stoeckel JA, Rehmann CR, Blodgett KD, Sparks RE, Padilla DK (2003) A developmental bottleneck in dispersing larvae: implications for spatial population dynamics. Ecol Lett 6:352–360CrossRefGoogle Scholar
  34. Sneyers R (1975) Sur l’analyse statistique des séries d’observations. Note technique 143. WMO, Geneva, SwitzerlandGoogle Scholar
  35. Sprung M (1993) The other life: an account of present knowledge of the larval phase of Dreissena polymorpha. In: Nalepa TF, Schloesser DW (eds) Zebra mussels: biology, impacts, and control. Lewis, Boca Raton, pp. 39–53Google Scholar
  36. Sprung M (1995) Physiological energetics of the zebra mussel Dreissena polymorpha in Lakes. 2. Food uptake and gross growth efficiency. Hydrobiologia 304:133–146CrossRefGoogle Scholar
  37. Stańczykowska A (1977) Ecology of Dreissena polymorpha (Pall.) (Bivalvia) in lakes. Polskie Archiwum Hysrobiologii 24:461–530Google Scholar
  38. Stańczykowska A, Lewandowski K (1993) Thirty years of studies of Dreissena polymorpha ecology in Mazurian lakes of northeastern Poland. In: Nalepa TF, Schloesser DW (eds) Zebra mussels: biology, impacts, and control. Lewis, Boca Raton, pp. 3–37Google Scholar
  39. Stoeckel JA, Padilla DK, Schneider DW, Rehmann CR (2004) Laboratory culture of Dreissena polymorpha larvae: spawning success, adult fecundity, and larval mortality patterns. Can J Zool 82:1436–1443CrossRefGoogle Scholar
  40. Stoeckmann AM, Garton DW (2001) Flexible energy allocation in zebra mussels (Dreissena polymorpha) in response to different environmental conditions. J North Am Benthol Soc 20:486–500CrossRefGoogle Scholar
  41. Vanderploeg HA, Liebig JR, Gluck AA (1996) Evaluation of different phytoplankton for supporting development of zebra mussel larvae (Dreissena polymorpha): the importance of size and polyunsaturated fatty acid content. J Great Lakes Res 22:36–45CrossRefGoogle Scholar
  42. Wacker A, von Elert E (2002) Strong influences of larval diet history on subsequent post-settlement growth in the freshwater mollusc Dreissena polymorpha. Proc R Soc Lond B Biol Sci 269:2113–2119CrossRefGoogle Scholar
  43. Walz N (1973) Studies on the biology of Dreissena polymorpha Pallas in the Lake of Constance. Arch Hydrobiol Suppl 42:452–482Google Scholar
  44. Wellborn GA (1994) Size-biased predation and prey life-histories: a comparative study of freshwater amphipod populations. Ecology 75:2104–2117CrossRefGoogle Scholar
  45. Wetzel RG (2001) Limnology: lake and river ecosystems. Academic, San DiegoGoogle Scholar
  46. Woynarovich E (1961) The oxygen consumption of Dreissena polymorpha (Lamellibranchiata) at different temperatures. Annales Instituti Biologici Tihany 28:211–216Google Scholar
  47. Wright DA, Setzler Hamilton EM, Magee JA, Kennedy VS, McIninch SP (1996) Effect of salinity and temperature on survival and development of young zebra (Dreissena polymorpha) and quagga (Dreissena bugensis) mussels. Estuaries 19:619–628CrossRefGoogle Scholar

Copyright information

© Springer-Verlag 2006

Authors and Affiliations

  1. 1.Leibniz Institute of Freshwater Ecology and Inland FisheriesBerlinGermany

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