Gourbière Sébastien, Menu Fréderic
Université de Perpignan Via Domitia; UMR 5244 CNRS-EPHE-UPVD, Laboratoire de Biologie et d'Ecologie Tropicale et Méditerranéenne, 52 Avenue Paul Alduy, 66860 Perpignan Cedex, France.
Evolution. 2009 Jul;63(7):1879-92. doi: 10.1111/j.1558-5646.2009.00731.x. Epub 2009 May 21.
Many plants, insects, and crustaceans show within-population variability in dormancy length. The question of whether such variability corresponds to a genetic polymorphism of pure strategies or a mixed bet-hedging strategy, and how the level of phenotypic variability can evolve remain unknown for most species. Using an eco-genetic model rooted in a 25-year ecological field study of a Chestnut weevil, Curculio elephas, we show that its diapause-duration variability is more likely to have evolved by the spread of a bet-hedging strategy than by the establishment of a genetic polymorphism. Investigating further the adaptive dynamics of diapause-duration variability, we find two unanticipated patterns of general interest. First, there is a trade-off between the ability of bet-hedging strategies to persist on an ecological time scale and their ability to invade. The optimal strategy (in terms of persistence) cannot invade, whereas suboptimal bet-hedgers are good invaders. Second, we describe an original evolutionary dynamics where each bet-hedging strategy (defined by its rate of prolonged diapause) resists invasion by all others, so that the first type of bet-hedger to appear persists on an evolutionary time scale. Such "evolutionary priority effect" could drive the evolution of maladapted levels of diapause-duration variability.
许多植物、昆虫和甲壳类动物在种群内部的休眠时长存在变异性。对于大多数物种而言,这种变异性是对应着纯策略的遗传多态性还是混合式的风险对冲策略,以及表型变异性水平如何进化,这些问题仍然未知。通过一个基于对栗实象甲(Curculio elephas)长达25年的生态实地研究的生态遗传模型,我们发现其滞育时长变异性更有可能是通过风险对冲策略的传播而非遗传多态性的建立而进化的。进一步研究滞育时长变异性的适应性动态,我们发现了两个普遍感兴趣的意外模式。首先,在风险对冲策略在生态时间尺度上的持续能力与其入侵能力之间存在权衡。最优策略(就持续性而言)无法入侵,而次优的风险对冲者是良好的入侵者。其次,我们描述了一种原始的进化动态,其中每种风险对冲策略(由其延长滞育的速率定义)都能抵抗其他所有策略的入侵,以至于最早出现的那种风险对冲者在进化时间尺度上得以持续存在。这种“进化优先效应”可能会推动滞育时长变异性的适应不良水平的进化。