Evolution as a critical component of plankton dynamics

Microevolution is typically ignored as a factor directly affecting ongoing population dynamics. We show here that density–dependent natural selection has a direct and measurable effect on a planktonic predator–prey interaction. We kept populations of Brachionus calyciflorus, a monogonont rotifer that exhibits cyclical parthenogenesis, in continuous flow–through cultures (chemostats) for more than 900 days. Initially, females frequently produced male offspring, especially at high population densities. We observed rapid evolution, however, towards low propensity to reproduce sexually, and by 750 days, reproduction had become entirely asexual. There was strong selection favouring asexual reproduction because, under the turbulent chemostat regime, males were unable to mate with females, produced no offspring, and so had zero fitness. In replicated chemostat experiments we found that this evolutionary process directly influenced the population dynamics. We observed very specific but reproducible plankton dynamics which are explained well by a mathematical model that explicitly includes evolution. This model accounts for both asexual and sexual reproduction and treats the propensity to reproduce sexually as a quantitative trait under selection. We suggest that a similar amalgam of ecological and evolutionary mechanisms may drive the dynamics of rapidly reproducing organisms in the wild.

[1]  G. Carvalho,et al.  The clonal ecology of Daphnia magna (Crustacea: Cladocera). I: Temporal changes in the clonal structure of a natural population , 1987 .

[2]  S. Ellner,et al.  Crossing the hopf bifurcation in a live predator-prey system. , 2000, Science.

[3]  Serra,et al.  Optimal rates of bisexual reproduction in cyclical parthenogens with density‐dependent growth , 1999 .

[4]  D. Reznick,et al.  The population ecology of contemporary adaptations: what empirical studies reveal about the conditions that promote adaptive evolution , 2004, Genetica.

[5]  Andrew P. Hendry,et al.  Contemporary evolution meets conservation biology , 2003 .

[6]  J. N. Thompson,et al.  Rapid evolution as an ecological process. , 1998, Trends in ecology & evolution.

[7]  T. Quinn,et al.  Rapid evolution of reproductive isolation in the wild: evidence from introduced salmon. , 2000, Science.

[8]  Alexander I Khibnik,et al.  Three mechanisms of Red Queen dynamics , 1997, Proceedings of the Royal Society of London. Series B: Biological Sciences.

[9]  D. Post,et al.  Lake ecosystems: Rapid evolution revealed by dormant eggs , 1999, Nature.

[10]  G. Carvalho,et al.  Sex, parthenogenesis and genetic structure of rotifers: microsatellite analysis of contemporary and resting egg bank populations , 2000, Molecular ecology.

[11]  I. Saloniemi,et al.  A Coevolutionary Predator-Prey Model with Quantitative Characters , 1993, The American Naturalist.

[12]  L. De Meester,et al.  Rapid, local adaptation of zooplankton behavior to changes in predation pressure in the absence of neutral genetic changes , 2001, Proceedings of the National Academy of Sciences of the United States of America.

[13]  Stephen P. Ellner,et al.  Living on the edge of chaos: population dynamics of fennoscandian voles , 2000 .

[14]  J. J. Gilbert Mictic female production in the rotifer Brachionus calyciflorus , 1963 .

[15]  M. Boraas Population dynamics of food‐limited rotifers in two‐stage chemostat culture1,2 , 1983 .

[16]  J. J. Gilbert Endogenous regulation of environmentally induced sexuality in a rotifer: a multigenerational parental effect induced by fertilisation , 2002 .

[17]  M. Boraas,et al.  A demographic profile of the fastest growing metazoan: a strain of Brachionus calyciflorus (Rotifera) , 1989 .

[18]  W. Gurney,et al.  Endogenous metabolism and the stability of microbial prey–predator systems , 1983, Biotechnology and bioengineering.

[19]  R. Lande NATURAL SELECTION AND RANDOM GENETIC DRIFT IN PHENOTYPIC EVOLUTION , 1976, Evolution; international journal of organic evolution.

[20]  Ross Ihaka,et al.  Gentleman R: R: A language for data analysis and graphics , 1996 .

[21]  H. Allen Orr ADAPTATION AND THE COST OF COMPLEXITY , 2000 .

[22]  T. Snell,et al.  Why are male rotifers dwarf? , 1998, Trends in ecology & evolution.

[23]  S. Boissinot,et al.  Evolutionary Biology , 2000, Evolutionary Biology.