2007
DOI: 10.1111/j.1365-294x.2007.03304.x
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Case studies and mathematical models of ecological speciation. 2. Palms on an oceanic island

Abstract: A recent study of a pair of sympatric species of palms on the Lord Howe Island is viewed as providing probably one of the most convincing examples of sympatric speciation to date. Here we describe and study a stochastic, individual-based, explicit genetic model tailored for this palms system. Overall, our results show that relatively rapid (<50,000 generations) colonization of a new ecological niche, and sympatric or parapatric speciation via local adaptation and divergence in flowering periods are theoretical… Show more

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Cited by 112 publications
(143 citation statements)
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“…Random genetic drift has previously been shown to accelerate the evolution of reproductive isolation by facilitating strong linkage disequilibrium between ecological and mating strategies (Dieckmann & Doebeli 1999;van Doorn & Weissing 2001) or fostering local adaptation to adjacent habitats differing in flowering time (Stam 1983). Previous models of sympatric speciation involved disruptive natural or sexual selection (Kondrashov & Kondrashov 1999;Drossel & McKane 2000;Doebeli & Dieckmann 2003;Bü rger et al 2006;Doebeli et al 2007;Gavrilets & Vose 2007;Leimar et al 2008). In those models, disruptive selection and reproductive isolation are caused by resource competition among similar phenotypes, displacement into distinct ecological niches or selective assortative mating.…”
Section: Discussionmentioning
confidence: 99%
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“…Random genetic drift has previously been shown to accelerate the evolution of reproductive isolation by facilitating strong linkage disequilibrium between ecological and mating strategies (Dieckmann & Doebeli 1999;van Doorn & Weissing 2001) or fostering local adaptation to adjacent habitats differing in flowering time (Stam 1983). Previous models of sympatric speciation involved disruptive natural or sexual selection (Kondrashov & Kondrashov 1999;Drossel & McKane 2000;Doebeli & Dieckmann 2003;Bü rger et al 2006;Doebeli et al 2007;Gavrilets & Vose 2007;Leimar et al 2008). In those models, disruptive selection and reproductive isolation are caused by resource competition among similar phenotypes, displacement into distinct ecological niches or selective assortative mating.…”
Section: Discussionmentioning
confidence: 99%
“…Examples of allochronic speciation are also expected in plants because assortative mating by flowering time is inevitable as mating can occur only among simultaneously open flowers ( Fox 2003;Weis et al 2005;Savolainen et al 2006;Gavrilets & Vose 2007). Although most studies on plant speciation have focused on prezygotic isolating mechanisms such as changes in self-fertilization rate, sex expression and pollinator or habitat specialization (Conner 2006), evidence also exists for temporal isolation.…”
Section: Introductionmentioning
confidence: 99%
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“…Flowering time differences between populations have also been reported in other Rhododendron species (Kudo, 1993;Kameyama et al, 2001;Mejías et al, 2002). The occurrence of reproductive isolation or reproductive incompatibility is related to assortative mating, because immigrants that flower at different times from those of local individuals cannot reproduce, and as a consequence no gene flow occurs (Gavrilets and Vose, 2007). Therefore, geographic variations in flowering rhythms of R. oldhamii suggest population isolation caused by reduced gene flow among populations.…”
Section: Introductionmentioning
confidence: 94%
“…The authors emphasized the importance of an environmentally induced shift in flowering for facilitating genetic divergence. However, if this effect was indeed present, then speciation was not sympatric but parapatric at least according to some definitions (Gavrilets & Vose, 2007).…”
Section: Introductionmentioning
confidence: 99%