Identification of trade-offs underlying the primary strategies of plants

Question: What are the key physiological and life-history trade-offs responsible for the evolution of different suites of plant traits (strategies) in different environments? Experimental methods: Common-garden experiments were performed on physiologically realistic model plants, evolved in contrasting environments, in computer simulations. This allowed the identification of the trade-offs that resulted in different suites of traits (strategies). The environments considered were: resource rich, low disturbance (competitive); resource poor, low disturbance (stressed); resource rich, high disturbance (disturbed); and stressed environments containing herbivores (grazed). Results: In disturbed environments, plants increased reproduction at the expense of ability to compete for light and nitrogen. In competitive environments, plants traded off reproductive output and leaf production for vertical growth. In stressed environments, plants traded off vertical growth and reproductive output for nitrogen acquisition, contradicting Grime's (2001) theory that slow-growing, competitively inferior strategies are selected in stressed environments. The contradiction is partly resolved by incorporating herbivores into the stressed environment, which selects for increased investment in defence, at the expense of competitive ability and reproduction. Conclusion: Our explicit modelling of trade-offs produces rigorous testable explanations of observed associations between suites of traits and environments.

[1]  J. P. Grime,et al.  A trade-off between scale and precision in resource foraging , 1991, Oecologia.

[2]  U. Schaffner,et al.  Do vigour of introduced populations and escape from specialist herbivores contribute to invasiveness? , 2005 .

[3]  R. Sibly,et al.  An allelocentric view of life-history evolution. , 1993, Journal of theoretical biology.

[4]  J. P. Grime,et al.  PLASTICITY AND LIGHT INTERCEPTION BY SIX BRYOPHYTES OF CONTRASTED ECOLOGY , 1989 .

[5]  Matt Aitkenhead,et al.  The emergence of primary strategies in evolving virtual-plant populations , 2003 .

[6]  James H. Brown,et al.  Life-history evolution under a production constraint , 2006, Proceedings of the National Academy of Sciences.

[7]  Robert W. Pearcy,et al.  Photosynthetic responses to dynamic light under field conditions in six tropical rainforest shrubs occuring along a light gradient , 1997, Oecologia.

[8]  J. P. Grime,et al.  Trait convergence and trait divergence in herbaceous plant communities: Mechanisms and consequences , 2006 .

[9]  A. Grant,et al.  Life History Evolution , 2002, Heredity.

[10]  J. P. Grime,et al.  The effects of trophic structure and soil fertility on the assembly of plant communities: a microcosm experiment , 2000 .

[11]  R. W. Pearcy,et al.  Photosynthetic Responses to Dynamic Light Environments by Hawaiian Trees : Time Course of CO(2) Uptake and Carbon Gain during Sunflecks. , 1985, Plant physiology.

[12]  L. Yampolsky,et al.  Life History Theory , 2003 .

[13]  Joseph M. Craine,et al.  Reconciling plant strategy theories of Grime and Tilman , 2005 .

[14]  J. P. Grime Plant strategy theories: a comment on Craine (2005) , 2007 .

[15]  D. Tilman Resource competition and plant traits: a response to Craine et al. 2005 , 2007 .

[16]  L. Oksanen,et al.  Exploitation Ecosystems in Gradients of Primary Productivity , 1981, The American Naturalist.

[17]  William M. Schaffer,et al.  Plant strategies and the dynamics and structure of plant communities , 1989 .

[18]  B. Enquist,et al.  Rebuilding community ecology from functional traits. , 2006, Trends in ecology & evolution.

[19]  R. Hunt,et al.  A self‐assembling model of resource dynamics and plant growth incorporating plant functional types , 2001 .

[20]  John L. Harper,et al.  Population Biology of Plants. , 1978 .

[21]  J. P. Grime,et al.  Seedling resistance to herbivory as a predictor of relative abundance in a synthesised prairie community , 2003 .