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Life history response of Daphnia galeata to heterogeneous conditions within a reservoir as determined in a cross-designed laboratory experiment

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Abstract

Growth and reproduction were studied in the laboratory in a cross-designed experimental set-up in four Daphnia galeata subpopulations collected from different locations (with respect to water characteristics) in a reservoir (epilimnion, metalimnion and hypolimnion in the deepest part of the reservoir near the dam and epilimnion of the upstream part of the reservoir) and in a laboratory clone of the same species. The results of two-way ANOVA revealed significant effects of the two parameters manipulated – source of water used for cultures and Daphnia subpopulation – on the life history characteristics of growth and reproduction. The water from the upstream part of the reservoir was the most favourable culture medium for all characteristics of the Daphnia groups studied (the largest primiparae, clutches and eggs, the shortest postembryonic development time and filtering setae). The poorest performances were recorded in the downstream, epilimnetic and metalimnetic waters. The primiparae in the hypolimnetic water were smaller but had relatively larger clutches of smaller eggs and slightly longer postembryonic development times. The Daphnia subpopulation originating from the hypolimnion had the smallest primiparae, the largest clutches, the smallest eggs and the shortest postembryonic development, whereas the opposite was found in animals from the epilmnion. These differences in ecologically relevant traits were supported by analysis of the quasi-neutral genetic markers that indicated significant site-dependent differences in clonal structure between the subpopulations. There was no consistent trend to higher within-group variance in the life history traits in the genetically heterogeneous subpopulations from the reservoir compared to the laboratory clone.

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References

  • Boersma M, Vijverberg J (1994) Resource depression in Daphnia galeata, Daphnia cucullata and their interspecific hybrid: life history consequences. J Plankton Res 16:1741–1758

    Article  Google Scholar 

  • Čech M, KubeČka J (2006) Ontogenetic changes in the bathypelagic behaviour of European perch fry Perca fluviatilis L. monitored by hydroacoustic methods. Biológia 61:211–219

    Google Scholar 

  • Čech M, Kratochvíl M, KubeČka J, Draštík V, Matěna J (2005) Diel vertical migrations of bathypelagic perch fry. J Fish Biol 66:685–702

    Article  Google Scholar 

  • Declerck S, Weber A (2003) Genetic differentiation in life history between Daphnia galeata populations: an adaptation to local predation regimes? J Plankton Res 25:93–102

    Article  CAS  Google Scholar 

  • Declerck S, Cousyn C, De Meester L (2001) Evidence for local adaptation in neighbouring Daphnia populations: a laboratory transplant experiment. Freshwater Biol 46:187–198

    Article  Google Scholar 

  • De Meester L (1996) Local genetic differentiation and adaptation in freshwater zooplankton populations: patterns and processes. Ecoscience 3:385–399

    Google Scholar 

  • De Meester L, Weider LJ (1999) Depth selection behavior, fish kairomones, and the life histories of Daphnia hyalina×galeata hybrid clones. Limnol Oceanogr 44:1248–1258

    Google Scholar 

  • DeMott RW, Edington JR, Tessier AJ (2004) Testing zooplankton food limitation across gradients of depth and productivity in small stratified lakes. Limnol Oceanogr 49:1408–1416

    Article  Google Scholar 

  • Ebert D (1991) The effect of size at birth, maturation threshold and genetic differences on the life-history of Daphnia magna. Oecologia 86:243–250

    Article  Google Scholar 

  • García-Ruiz R, Lucena J, Niell FX (1999) Do bacteria regenerate phosphorus while decomposing seston? Mar Freshwater Res 50:459–466

    Google Scholar 

  • Hebert PDN, Beaton MJ (1989) Methodologies for allozyme analysis using cellulose acetate electrophoresis. Helena Laboratories, Beaumont, Tex.

    Google Scholar 

  • Hejzlar J, Straškraba M (1989) On the horizontal distribution of limnological variables in Římov and other stratified Czechoslovak reservoirs. Arch Hydrobiol Beih Ergebn Limnol 33:41–55

    Google Scholar 

  • Hessen DO, Andersen T (1990) Bacteria as a source of phosphorus for zooplankton. Hydrobiologia 206:217–223

    CAS  Google Scholar 

  • Hrbáček J (1977) Competition and predation in relation to species composition of freshwater zooplankton, mainly Cladocera. In: Cairns J (ed) Aquatic microbial communities. Garland Publ, New York, London, pp 305–353

    Google Scholar 

  • Hrbáčková M (1971) The size distribution of neonates and growth of Daphnia hyalina Leydig (Crustacea, Cladocera) from Lake Maggiore under laboratory conditions. Mem Ist Ital Idrobiol 27:357–367

    Google Scholar 

  • Hrbáčková-Esslová M (1963) The development of three species of Daphnia in the surface water of the Slapy reservoir. Int Rev Ges Hydrobiol 48:325–333

    Article  Google Scholar 

  • Jacobs J (1980) Environmental control of cladoceran cyclomorphosis via target-specific growth factors in the animal. In: Kerfoot WC (ed) Evolution and ecology of zooplankton communities. University Pressof New England, Hanover, N.H., pp 429–437

    Google Scholar 

  • Kořínek V, Křepelová-Macháčková B, Macháček J (1986) Filtering structures of Cladocera and their ecological significance. II. Relation between the concentration of seston and the size of filtering combs in some species of the genera Daphnia and Ceriodaphnia. Věst čs Spol Zool 50:255–258

    Google Scholar 

  • Kubečka J, Wittingerová M (1998) Horizontal beaming as a crucial component of acoustic fish stock assessment in freshwater reservoirs. Fish Res 35:99–106

    Article  Google Scholar 

  • Lampert W (1977) Studies on the carbon balance of Daphnia pulex DeGeer as related to environmental conditions. II. The dependence of carbon assimilation on animal size, temperature, food concentration and diet species. Arch Hydrobiol Suppl 48:310–335

    CAS  Google Scholar 

  • Lampert W (1987) Feeding and nutrition in Daphnia. Mem Ist Ital Idrobiol 45:143–192

    Google Scholar 

  • Lampert W (1994) Phenotypic plasticity in the size at first reproduction in Daphnia magna. Verh Int Verein Limnol 25:2362–2365

    Google Scholar 

  • Lass S, Spaak P (2003) Temperature effects on chemical signalling in a predator–prey system. Freshwater Biol 48:669–677

    Article  CAS  Google Scholar 

  • Lynch M (1987) The consequences of fluctuating selection for isozyme polymorphism in Daphnia. Genetics 115:657–669

    PubMed  CAS  Google Scholar 

  • Lynch M (1989) The life history consequences of resource depression in Daphnia pulex. Ecology 70:246–256

    Article  Google Scholar 

  • Lynch M, Ennis R (1983) Resource availability, maternal effects, and longevity. Exp Gerontol 18:147–165

    Article  PubMed  CAS  Google Scholar 

  • Lund JWG, Kipling C, Le Gren GA (1958) The inverted microscope method of estimating algal numbers and the statistical basis of estimation by counting. Hydrobiologia 11:143–170

    Article  Google Scholar 

  • Macháček J (1991) Indirect effect of planktivorous fish on the growth and reproduction of Daphnia galeata. Hydrobiologia 225:193–197

    Article  Google Scholar 

  • Macháček J (1993) Comparison of the response of Daphnia galeata and Daphnia obtusa to fish-produced chemical substance. Limnol Oceanogr 38:1544–1550

    Article  Google Scholar 

  • Macháček J (1998) What can we learn from Daphnia filtering screens? J Plankton Res 20:1645–1650

    Article  Google Scholar 

  • Macháček J (2001) Daphnia galeata life history response to heterogeneous food conditions and dissolved chemicals in the reservoir. Hydrobiologia 442:215–222

    Article  Google Scholar 

  • Macháček J, Sed’a J (1998) Spatio-temporal changes of morphological and life history parameters of Daphnia galeata in a canyon-shaped reservoir. Int Rev Ges Hydrobiol 83:171–178

    Google Scholar 

  • Macháček J, Sed’a J (2002) Diurnal aspect of vertical distribution of Daphnia species in the Římov Reservoir in the spring period. In: 4th Int Conf Reservoir Limnol Water Quality Extended Abstr. české Budějovice, Czech Republic, pp 204–206

  • Mitchell SE, Halves J, Lampert W (2004) Coexistence of similar genotypes of Daphnia magna in intermittent populations: response to thermal stress. Oikos 106:469–478

    Article  Google Scholar 

  • Mort MA, Wolf HG (1986) The genetic structure of large-lake Daphnia populations. Evolution 40:756–766

    Article  Google Scholar 

  • Müller-Navarra DC (1995) Biochemical versus mineral limitation in Daphnia. Limnol Oceanogr 40:1209–1214

    Google Scholar 

  • Pont D, Amrani J (1990) The effects of selective fish predation on the horizontal distribution of pelagic Cladocera in a southern French reservoir. Hydrobiologia 207:259–267

    Article  Google Scholar 

  • Repka S, Vesela S, Weber A, Schwenk K (1999) Plasticity in filtering screens of Daphnia cucullata×galeata hybrids and parental species at two food concentrations. Oecologia 120:485–491

    Article  Google Scholar 

  • Ringelberg J (1991) Enhancement of the phototactic reaction in Daphnia hyalina by a chemical mediated by juvenile perch (Perca fluviatilis). J Plankton Res 13:17–25

    Article  Google Scholar 

  • Sed’a J, Macháček J (1998) The effect of flow-through regime on zooplankton dynamics in a canyon-shaped dam reservoir. Int Rev Ges Hydrobiol 83:477–484

    Google Scholar 

  • Sommer U, Gliwicz ZM, Lampert W, Duncan A (1986) The PEG-model of seasonal succession of planktonic events in fresh waters. Arch Hydrobiol 106:433–471

    Google Scholar 

  • Spaak P, Hoekstra JR (1995) Life history variation and the coexistence of a Daphnia hybrid with its parental species. Ecology 76:553–564

    Article  Google Scholar 

  • Urabe J (1990) Stable horizontal variation in the zooplankton community structure of a reservoir maintained by predation and competition. Limnol Oceanogr 35:1703–1717

    Google Scholar 

  • Weglenska T (1971) The influence of various concentrations of natural food on the development, fecundity, and production of planktonic crustacean filtrators. Ekol Pol 19:427–471

    Google Scholar 

  • Weider LJ (1985) Spatial and temporal genetic heterogeneity in a natural Daphnia population. J Plankton Res 7:101–123

    Article  Google Scholar 

  • Weider JL, Stich HB (1992) Spatial and temporal heterogeneity of Daphnia in Lake Constance; intra- and interspecific comparisons. Limnol Oceanogr 37:1327–1334

    Article  Google Scholar 

  • Winder M, Boersma M, Spaak P (2003) On the cost of vertical migration: are feeding conditions really worse at greater depths? Freshwater Biol 48:383–393

    Article  Google Scholar 

Download references

Acknowledgements

The authors are grateful to J. Zemanová for technical assistance during the experimental work. J. Komárková is thanked for processing the phytoplankton samples and M. Vožechová and V. Hejzlarová for doing the chemical analyses. J. Hrbáček and V. Kořínek are thanked for a critical reading of the earlier version of the manuscript. J. Lepš is thanked for his help with statistical analysis of the data and M. Burgis for the linguistic revision of the text. Two anonymous reviewers are thanked for careful reviews and valuable comments, which considerably improved the manuscript. The work was financially supported by the Grant Agency of the Czech Republic, Grants No. 206/03/1537 and 206/04/0190 and Grant Agency of the Academy of Sciences of the Czech Republic, grant No. A6017301.

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Correspondence to Jiří Macháček.

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Macháček, J., Sed’a, J. Life history response of Daphnia galeata to heterogeneous conditions within a reservoir as determined in a cross-designed laboratory experiment. Aquat Ecol 41, 55–66 (2007). https://doi.org/10.1007/s10452-006-9045-3

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  • DOI: https://doi.org/10.1007/s10452-006-9045-3

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