The Relative Importance of Competition and Predation Varies with Productivity in a Model Community

Recent theory predicts that productivity can influence the relative importance of predation and competition in determining patterns in abundance, diversity, and community structure. In low‐productivity systems, competition is predicted to be the major influence on community patterns, while at high productivity, the major influence is predicted to be predation. We directly tested this theory using a laboratory model community. Our model community consisted of the bacteriophage T2 (a virus that feeds on Escherichia coli) and two populations of E. coli, in glucose‐limited chemostats. One E. coli population consisted of individuals that were sensitive to predation by T2 (“vulnerable” E. coli), and the other population consisted of individuals that were partially resistant to predation by T2 (“less vulnerable” E. coli). We manipulated productivity in this experiment by running replicate chemostats with different input concentrations of glucose. Our observations were consistent with theoretical predictions. We observed the decline of the more vulnerable prey population at higher productivity but not at lower productivity, and the decline of the less vulnerable prey population at lower productivity but not at higher productivity. However, the rate of decline in some replicates was slower than predicted, and extinctions were not observed during the experiments, contrary to theoretical predictions. We present some testable hypotheses that might explain the slow rate of decline observed.

[1]  R. Lenski,et al.  Effect of Prey Heterogeneity on the Response of a Model Food Chain to Resource Enrichment , 1999, The American Naturalist.

[2]  Richard E. Lenski,et al.  Effect of resource enrichment on a chemostat community of bacteria and bacteriophage , 1997 .

[3]  H. Godfray,et al.  Trade-off between parasitoid resistance and larval competitive ability in Drosophila melanogaster , 1997, Nature.

[4]  Michael L. Rosenzweig,et al.  Species Diversity in Space and Time , 1997 .

[5]  J. Mittler,et al.  Host-Parasite Coexistence: The Role of Spatial Refuges in Stabilizing Bacteria-Phage Interactions , 1996, The American Naturalist.

[6]  Mathew A. Leibold,et al.  A Graphical Model of Keystone Predators in Food Webs: Trophic Regulation of Abundance, Incidence, and Diversity Patterns in Communities , 1996, The American Naturalist.

[7]  Mark V. Lomolino,et al.  Species Diversity in Space and Time. , 1996 .

[8]  J. Grover Competition, Herbivory, and Enrichment: Nutrient-Based Models for Edible and Inedible Plants , 1995, The American Naturalist.

[9]  James P. Grover,et al.  Simple Rules for Interspecific Dominance in Systems with Exploitative and Apparent Competition , 1994, The American Naturalist.

[10]  T. Nakajima,et al.  Evolutionary Changes of Ecological Traits of Bacterial Populations through Predator-Mediated Competition 1. Experimental Analysis , 1994 .

[11]  T. Nakajima,et al.  Evolutionary Changes of Ecological Traits of Bacterial Populations through Predator-Mediated Competition 2. Theoretical Considerations , 1994 .

[12]  Richard E. Lenski,et al.  Long-Term Experimental Evolution in Escherichia coli. II. Changes in Life-History Traits During Adaptation to a Seasonal Environment , 1994, The American Naturalist.

[13]  J. Drake,et al.  Molecular Biology of Bacteriophage T4 , 1994 .

[14]  Edward McCauley,et al.  Sigmoid Relationships between Phosphorus, Algal Biomass, and Algal Community Structure , 1992 .

[15]  M. Power,et al.  TOP-DOWN AND BOTTOM-UP FORCES IN FOOD WEBS: DO PLANTS HAVE PRIMACY? , 1992 .

[16]  R. Lenski,et al.  Long-Term Experimental Evolution in Escherichia coli. I. Adaptation and Divergence During 2,000 Generations , 1991, The American Naturalist.

[17]  M. A. Leibold,et al.  Resource Edibility and the Effects of Predators and Productivity on the Outcome of Trophic Interactions , 1989, The American Naturalist.

[18]  R. Lenski EXPERIMENTAL STUDIES OF PLEIOTROPY AND EPISTASIS IN ESCHERICHIA COLI. I. VARIATION IN COMPETITIVE FITNESS AMONG MUTANTS RESISTANT TO VIRUS T4 , 1988, Evolution; international journal of organic evolution.

[19]  L. Chao,et al.  The effects of wall populations on coexistence of bacteria in the liquid phase of chemostat cultures. , 1985, Journal of general microbiology.

[20]  R. Lenski,et al.  Constraints on the Coevolution of Bacteria and Virulent Phage: A Model, Some Experiments, and Predictions for Natural Communities , 1985, The American Naturalist.

[21]  R. Lenski Two-step resistance by Escherichia coli B to bacteriophage T2. , 1984, Genetics.

[22]  Dm Jones,et al.  Fundamentals of Oncology , 1981 .

[23]  R. Holt Predation, apparent competition, and the structure of prey communities. , 1977, Theoretical population biology.

[24]  F. M. Stewart,et al.  Resource-Limited Growth, Competition, and Predation: A Model and Experimental Studies with Bacteria and Bacteriophage , 1977, The American Naturalist.

[25]  R. Ricklefs,et al.  Competition and the structure of bird communities. , 1975, Monographs in population biology.

[26]  S. Dodson,et al.  Predation, Body Size, and Composition of Plankton. , 1965, Science.

[27]  J. Monod The Growth of Bacterial Cultures , 1949 .

[28]  J. Grover Resource Competition , 1997, Population and Community Biology Series.

[29]  E. Simms,et al.  Costs of plant resistance to herbivory. , 1992 .

[30]  G. Stent,et al.  On the two step nature of bacteriophage absorption. , 1952, Biochimica et biophysica acta.