Predator-induced bottom-up effects in oligotrophic systems
- 73 Downloads
- 11 Citations
Abstract
Five treatments (replication n=2) were applied to mesocosms in an oligotrophic lake (TP=6–10 µg 1∼-1) to assess the effects of fish on planktonic communities. The treatments were: (1) high fish (30 kg ha−1Lepomis auritus, Linnaeus), (2) low fish (10 kg ha−1), (3) high removal of zooplankton, (4) low removal of zooplankton and (5) control. Total phosphorus, chlorophyll a, zooplankton biomass, and species richness decreased from high fish > low fish > control > low removal > high removal treatments. The fish treatments were dominated by crustacean zooplankton, while rotifers outnumbered the other zooplankters in the removal treatments. Calculations of zooplankton grazing rates suggested that clearance rates seldom exceeded 2% of the enclosure volume d−1 and were unlikely to have had much influence on phytoplankton biomass. Calculations from a phosphorus bioenergetics model revealed that when fish were present, their excretion rates were higher than the rates ascribed to zooplankton. Diet analysis showed that the fish derived most of their energy from the benthos and periphyton, and that fish excretion and egestion made significant contributions to the very oligotrophic pelagic phosphorus pool. In the absence of fish, zooplankton excretion was highest in the control treatments and lowest in the zooplankton removal treatments. Our results suggest that in oligotrophic systems, planktivorous fish can be significant sources of phosphorus and that fish and zooplankton induced nutrient cycling have significant impacts on planktonic community structure.
Key words
trophic cascade aquatic communities food webs phosphorus cyclingPreview
Unable to display preview. Download preview PDF.
References
- APRA (American Public Health Association), 1985. Standard methods for the examination of water and waste water, 16th edn. APHA, AWWA, WPCF Washington, DC.Google Scholar
- Balcer, M. D., N. L. Korda & S. I. Dodson, 1984. Zooplankton of the Great Lakes: a guide to the identification and ecology of the common crustacean species. University of Wisconsin Press, Madison.Google Scholar
- Bogdan, K. G., J. G. Gilbert & P. L. Starkweather, 1980. In situ clearance rates of planktonic rotifers. Hydrobiologia 73: 73–77.Google Scholar
- Brooks, J. L. & S. I. Dodson, 1965. Predation, body size, and composition of zooplankton. Science 150: 28–35.Google Scholar
- Carpenter, S. R. (ed.), 1988. Complex interactions in lake communities. Springer-Verlag, New York.Google Scholar
- Carpenter, S. R. & J. F. Kitchell (ededs), 1993. The trophic cascade in lakes. Cambridge.Google Scholar
- Carpenter, S. R., J. F. Kitchell & J. R. Hodgson, 1985. Cascading trophic interactions and lake productivity. BioScience 35: 634–638.Google Scholar
- Carpenter, S. R., J. F. Kitchell, J. R. Hodgson, P. A. Cochran, J. J. Elser, M. M. Elser, D. M. Lodge, D. K. Kretchmer, X. He & C. N. von Ende, 1987. Regulation of lake primary productivity by food web structure. Ecology 68: 1863–1876.Google Scholar
- Chow-Fraser, P, 1986. An empirical model to predict in situ grazing rates of Leptodiaptomus minutus Lilljeborg on small algal particles. Can. J. Fish. aquat. Sci. 43: 1065–1070.Google Scholar
- Chow-Fraser, P. & R. Knoechel, 1985. Factors regulating in situ filtering rates of Cladocera. Can. J. Fish. aquat. Sci. 42: 567–576.Google Scholar
- Edmondson, W. T. (ed.), 1959. Freshwater biology, 2nd edn. Wiley, New York.Google Scholar
- Elliot, J. M. & L. Persson, 1978. The estimation of daily rates of food consumption for fish. J. anim. Ecol. 47: 977–991.Google Scholar
- Hamilton, D. T. & W. D. Taylor, 1987. Short-term effects of zooplankton manipulations on phosphate uptaKe. Can. J. Fish. aquat. Sci. 44: 1038–1044.Google Scholar
- Heady, H. F., 1942. Littoral vegetation on the lakes of the Huntington Forest. Roosevelt Wildlife Bull. 8. 33 pp.Google Scholar
- Hewett, S. W. & B. L. Johnson, 1992. Fish bioenergetics model 2: an upgrade of a generalized bioenergetics model of fish growth for microcomputers. University of Wisconsin Sea Grant Institute, Madison.Google Scholar
- Kerfoot, W. C. & A. Sih (eds), 1987. Predation: direct and indirect impacts on aquatic communities. University Press of New England, Hanover. 386 pp.Google Scholar
- Kitchell, J. F., J. F. Koonce, R. V. O'Neill, H. H. Shugart Jr., J. J. Magnuson & R. S. Booth, 1974. Model of fish Biomass dynamics. Trans. am. Fish. Soc. 103: 786–798.CrossRefGoogle Scholar
- Knoechel, R. & L. B. Holtby, 1986. Construction and validation of a body-length-based model for the prediction of cladoceran community filtering rates. Limnol. Oceanogr. 31: 1–16.Google Scholar
- Kraft, C. E., 1992. Estimates of phosphorus cycling by fish using a bioenergetics approach. Can. J. Fish. aquat. Sci. 49: 1–9.Google Scholar
- Lehman, J. T., 1980. Release and cycling of nutrients between planktonic algae and herbivores. Limnol. Oceanogr. 25: 620–632.Google Scholar
- Lorenzen, C. J., 1967. Determination of chlorophyll and pheopigments: spectrophotometric equations. Limnol. Oceanogr. 12: 343–346.Google Scholar
- Lynch, M. & J. Shapiro, 1981. Predation, enrichment, and phytoplankton community structure. Limnol. Oceanogr. 26: 86–102.Google Scholar
- Mazumder, A., D. J. McQueen, W. D. Taylor & D. R. S. Lean, 1988. Effects of fertilization and planktivorous fish (yellow perch) predation on size distribution of particulate phosphorus and assimilated phosphate: Large enclosure experiments. Limnol. Oceanogr. 33: 421–430.Google Scholar
- McCauley, E. & F. Briand, 1979. Zooplankton grazing and phytoplankton species richness: field tests of the predation hypothesis. Limnol. Oceanogr. 24: 243–252.Google Scholar
- McCauley, E. & J. Kalff, 1987. Effect of changes in zooplankton on orthophosphate dynamics of natural phytoplankton communities. Can. J. Fish. aquat. Sci. 44: 176–182.Google Scholar
- McQueen, D. J., R. France & C. E. Kraft, 1992. Confounded impacts of planktivorous fish on freshwater biomanipulations. Arch. Hydrobiol. 125: 1–24.Google Scholar
- McQueen, D. J., J. R. Post & E. L. Mills, 1986. Trophic interactions in freshwater pelagic ecosystems. Can. J. Fish. aquat. Sci. 43: 1571–1581.Google Scholar
- Meijer, M. L. M. W. de Haan, A. W. Breukelaar & H. Buiteveld, 1990. Is reduction of the benthivorous fish an important cause of high transparency following biomanipulation in shallow lakes? Hydrobiologia 200/201 (Dev. Hydrobiol. 61): 303–315.Google Scholar
- Meredith, M. P. & S. V. Stehman, 1991. Repeated measures experiments in forestry: focus on analysis of response curves. Can. J. For. Res. 21: 957–965.Google Scholar
- Mills, E. L. & J. L. Confer, 1986. Computer processing of zooplankton/application in fisheries. Fisheries 11: 24–27.CrossRefGoogle Scholar
- Nakashima, B. S. & W. C. Legget, 1980. The role of fishes in the regulation of phosphorus availability in lakes. Can. J. Fish. aquat. Sci. 37: 1540–1549.Google Scholar
- Pace, M. L. & E. Funke, 1991. Regulation of planktonic microbial communities by nutrients and herbivores. Ecology 72: 904–914.Google Scholar
- Pace, M. L., G. B. McManus & S. E. G. Findlay, 1990. Planktonic community structure determines the fate of bacterial production in a temperate lake. Limnol. Oceanogr. 35: 795–808.Google Scholar
- Pennak, R. W., 1989. Fresh-water invertebrates of the United States. Protozoa to Mollusca, 3rd edn. Wiley, New York.Google Scholar
- Persson, L., G. Andersson, S. F. Hamrin & L. Johansson, 1988. Predator regulation and primary production along the productivity gradient of temperate lake ecosystems. In S. R. Carpenter (ed.), Complex interactions in lake communities, Springer-Verlag, New York: 45–46.Google Scholar
- Peters, R. H. & J. A. Downing, 1984. Empirical analysis of zooplankton filtering and feeding rates. Limnol. Oceanogr. 29: 763–778.Google Scholar
- Reynolds, C. S., 1984. The ecology of freshwater phytoplankton. Cambridge, 384 pp.Google Scholar
- SAS Institute Inc., 1990. SAS user's guide: Statistics. SAS Institute, Cary, N.C.Google Scholar
- Scavia, D. & G. A. Laird, 1987. Bacterioplankton in Lake Michigan: Dynamics, controls, and significance to carbon flux. Limnol. Oceanogr. 32: 1017–1032.Google Scholar
- Scavia, D., D. A. Laird & G. L. Fahnenstiel, 1986. Production of planktonic bacteria in Lake Michigan. Limnol. Oceanogr. 31: 612–626.Google Scholar
- Seaburg, K. G. & J. B. Moyle, 1964. Feeding habits of the warmwater fishes. Trans. am. Fish. Soc. 93: 280–285.Google Scholar
- Shapiro, J. & D. I. Wright, 1984. Lake restoration by biomanipulation. Round Lake, Minnesota: the first two years. Freshwat. Biol. 14: 371–383.Google Scholar
- Simberloff, D., 1972. Properties of the rarefaction diversity measurement. Am. Nat. 106: 414–418.CrossRefGoogle Scholar
- Taylor, W. D. & D. R. S. Lean, 1991. Phosphorus pool sizes and fluxes in the epilimnion of a mesotrophic lake. Can. J. Fish. aquat. Sci. 48: 1293–1301.Google Scholar
- Vanni, M. J., 1987. Indirect effect of predators on age-structured prey populations: planktivorous fish and zooplankton. In W. C. Kerfoot & A. Sih (eds), Predation: direct and indirect impacts on aquatic communities, University Press of New England, Hanover: 149–160.Google Scholar
- Vanni, M. J. & D. L. Findlay, 1990. Trophic cascades and phytoplankton community structure. Ecology 71: 921–937.Google Scholar
- Wetzel, R. G. & G. E. Likens, 1991. Limnological analyses, 2nd edn. Springer-Verlag, New York.Google Scholar
- Zaret, T. M., 1980. Predation and freshwater communities. Yale University Press, New Haven.Google Scholar