BOTTOM-UP AND TOP-DOWN IMPACTS ON FRESHWATER PELAGIC COMMUNITY STRUCTURE'

For freshwater pelagic ecosystems, the biodiversity and cascading trophic interaction theories both predict that decreased piscivore populations will result in direct, short—term (a few years) increases in planktivore biomass, reductions in crustacean herbivore biomass, and increases in chlorophyll a concentration and phytoplankton biomass. An Alternate view is offered by the bottom—up:top—down theory, which predicts that in eutrophic lakes changes in piscivore biomasses will have strong impacts on planktivore numbers, weaker but observable impacts on zooplankton biomass, and little or no long—term effects on phytoplankton biomass. A partial winterkill at Lake St. George, Ontario, Canada allowed us to test these predictions. The data set comprised measures of: (1) piscivore and planktivore numbers, (2) zooplankton species composition, size structure, and biomass, (3) chlorophyll a concentration and Secchi depth, and (4) water chemistry from 1980 through 1986. Prior to the winterkill of 1981—1982, the piscivore population was high (1000—2000 piscivores/ha), the planktivore population was intermediate (8000—10 000 planktivores/ha), zooplankton biomass was intermediate (2400 µg/L), and chlorophyll a concentration was high (5—12 µg/L). In the year following the winterkill (1982), piscivore and planktivore numbers were low, and zooplankton biomass and chlorophyll a concentration were high. During the next 2 yr (1983—1984) the planktivore population increased rapidly to densities >20 000 individuals/ha, zooplankton biomass density decreased to <1600 µg/L and chlorophyll a concentration decreased. During the final 2 yr of the study, piscivores recruited to near prewinterkill levels, planktivores were reduced to <8000 individuals/ha, zooplankton biomass increased, and chlorophyll a concentration decreased. Over the 7 yr data set, we found a strong negative correlation between numbers of piscivores and planktivores, a weaker correlation between numbers of planktivores and zooplankton biomass, and no between—year correlation between zooplankton biomass and chlorophyll a concentration. There was, however, a positive correlation between total epilimnetic phosphorus and chlorophyll a concentration. These data are consistent with predictions made by the bottom—up:top—down model, and the implication is that at Lake St. George, the trophic cascade uncouples at the zooplankton → phytoplankton link. We speculate that this may be due to the combined effects of lake trophy and Daphnia species composition and size.

[1]  A. Jensen,et al.  Algal Competition for Phosphorus: The Influence of Zooplankton and Fish , 1986 .

[2]  J. Post,et al.  The impact of planktivorous flsh on the structure of a plankton community , 1987 .

[3]  B. Moss,et al.  The Role of Predation in Causing Major Changes in the Limnology of a Hyper‐Eutrophic Lake , 1980 .

[4]  W. Kerfoot,et al.  Ability of Daphnia to buffer trout lakes against periodic nutrient inputs: With 2 figures in the text , 1985 .

[5]  Stephen R. Carpenter,et al.  Cascading Trophic Interactions and Lake Productivity , 1985 .

[6]  Ray W. Drenner,et al.  Experimental Analysis of the Direct and indirect Effects of an Omnivorous Filter-Feeding Clupeid on Plankton Community Structure , 1986 .

[7]  G. Fahnenstiel,et al.  Influence of Salmonine Predation and Weather on Long-Term Water Quality Trends in Lake Michigan , 1986 .

[8]  W. G. Sprules,et al.  A microcomputer-based measuring device for biological research , 1981 .

[9]  A. Chau,et al.  A semi-automated method for the determination of inorganic, organic and total phosphate in sediments. , 1976, The Analyst.

[10]  David I. Wright Lake restoration by biomanipulation: Round Lake, Minnesota, the first two years , 1984 .

[11]  F. Rahel Factors Structuring Fish Assemblages Along a Bog Lake Successional Gradient , 1984 .

[12]  J. Greenbank Limnological Conditions in Ice‐Covered Lakes, Especially as Related to Winter‐Kill of Fish , 1945 .

[13]  Hakumat Rai,et al.  Phytoplankton control by grazing zooplankton: A study on the spring clear‐water phase1 , 1986 .

[14]  Stanford H. Smith Species Interactions of the Alewife in the Great Lakes , 1970 .

[15]  John R. Post,et al.  Trophic Relationships in Freshwater Pelagic Ecosystems , 1986 .

[16]  K. Porter plant animal interface in freshwater ecosystems , 1977 .

[17]  C. Walters,et al.  Equilibrium Models for Seasonal Dynamics of Plankton Biomass in Four Oligotrophy Lakes , 1987 .

[18]  L. Crowder,et al.  Forage Fishes and Their Salmonid Predators in Lake Michigan , 1981 .

[19]  G. P. Cooper,et al.  Relation of Dissolved Oxygen to Winter Mortality of Fish in Michigan Lakes , 1949 .

[20]  J. Magnuson,et al.  Patterns in the Species Composition and Richness of Fish Assemblages in Northern Wisconsin Lakes , 1982 .

[21]  J. Benndorf,et al.  Manipulation of the Pelagic Food Web by Stocking with Predacious Fishes , 1984 .

[22]  J. Casselman,et al.  Selective fish mortality resulting from low winter oxygen: With 8 figures in the text , 1975 .

[23]  D. Schindler Two Useful Devices for Vertical Plankton and Water Sampling , 1969 .

[24]  W. R. Demott SEASONAL SUCCESSION IN A NATURAL DAPHNIA ASSEMBLAGE , 1983 .

[25]  E. Lammens,et al.  Resource Partitioning and Niche Shifts of Bream (Abramis brama) and Eel (Anguilla anguilla) Mediated by Predation of Smelt (Osmerus eperlanus) on Daphnia hyalina , 1985 .

[26]  W. V. Densen,et al.  The role of the fish in the foodweb of Tjeukemeer, The Netherlands: With 1 figure and 2 tables in the text , 1984 .

[27]  Edward L. Mills,et al.  Impact on Daphnia pulex of Predation by Young Yellow Perch in Oneida Lake, New York , 1983 .

[28]  K. Hambright,et al.  Experimental study of the impacts of bluegill (Lepomis macrochirus) and largemouth bass (Micropterus salmoides) on pond community structure , 1986 .

[29]  M. Lynch Predation, competition, and zooplankton community structure: An experimental study1,2 , 1979 .

[30]  J. Shapiro,et al.  Biomanipulation: an ecosystem approach to lake restoration , 1975 .

[31]  Petter Larsson,et al.  THE SIGNIFICANCE OF THE PREDATOR FOOD CHAIN IN LAKE METABOLISM , 1980 .

[32]  A. Bonar Relations Between Exploitation, Yield, and Community Structure in Polish Pikeperch (Stizostedion lucioperca) Lakes, 1966–71 , 1977 .

[33]  D. Lean,et al.  Influence of water temperature and nitrogen to phosphorus ratios on the dominance of blue green algae in Lake St. George, Ontario , 1987 .

[34]  D. J. Hall,et al.  The Size-Efficiency Hypothesis and the Size Structure of Zooplankton Communities , 1976 .

[35]  S. Carpenter,et al.  Regulation of Lake Primary Productivity by Food Web Structure. , 1987, Ecology.

[36]  V. Lamarra Digestive activities of carp as a major contributor to the nutrient loading of lakes , 1975 .

[37]  M. Lynch,et al.  Predation, enrichment, and phytoplankton community structure1 , 1981 .

[38]  J. Shapiro The Importance of Trophic-Level Interactions to the Abundance and Species Composition of Algae in Lakes , 1980 .