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| speciation_and_plasticity [2013/02/14 10:46] – [Secondary-contact scenario] mkopp | speciation_and_plasticity [2019/03/21 09:21] (current) – external edit 127.0.0.1 | ||
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| ===== Background and general question ===== | ===== Background and general question ===== | ||
| - | * Speciation is a key topic in evolutionary biology (e.g. Coyne and Orr), and one in which mathematical modeling has for a long time played | + | * Speciation |
| - | * Traditionally, | + | * The reason is that speciation |
| - | * Another | + | * Here, we propose to develop mathematical models that will shed light on a topic of much recent |
| - | * Plasticity | + | * A **species** is most commonly defined as a group inter-fertile individuals that cannot reproduce with members of other species (Mayr 1942). Thus, understanding speciation requires understanding the evolution of reproductive isolation. |
| - | * Recently, plasticity has been advertised by some as a centerpiece of an " | + | * According to the traditional view, speciation almost always requires a geographic barrier separating the range of an ancestral species (allopatric speciation). Two independently evolving subpopulations will then diverge between the nascent species (allopatric speciation) and become more and more incompatible, |
| - | * General thrust: Plasticity | + | * However, there is mounting evidence for the opposing view that speciation is also without a strict geographic barrier (parapatric or sympatric speciation). Such " |
| - | * Wrt speciation, plasticity is thought to facilitate phenotypic/ | + | |
| + | * **Phenotypic plasticity** | ||
| + | * Recently, plasticity has been advertised by some as a centerpiece of an " | ||
| + | * The main argument is that plasticity | ||
| + | * In the context | ||
| * However, many proposed scenarios rely on verbal models, and many details remain unclear. This is particularly true for scenarios involving plasticity in an ecological adaptation trait (but see Thibert-Plante and Hendry 2011). | * However, many proposed scenarios rely on verbal models, and many details remain unclear. This is particularly true for scenarios involving plasticity in an ecological adaptation trait (but see Thibert-Plante and Hendry 2011). | ||
| * Open questions include: | * Open questions include: | ||
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| * Under what conditions does plasticity facilitate or impede the evolution of reproductive isolation in the presence of gene flow? | * Under what conditions does plasticity facilitate or impede the evolution of reproductive isolation in the presence of gene flow? | ||
| * If plastic traits themselves contribute to RI, what are the interactions between the evolution of environmentally and genetically induced reproductive barriers (see Fitzpatrick 2012)? | * If plastic traits themselves contribute to RI, what are the interactions between the evolution of environmentally and genetically induced reproductive barriers (see Fitzpatrick 2012)? | ||
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| ===== Outline of project ===== | ===== Outline of project ===== | ||
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| * Key questions include: | * Key questions include: | ||
| * What will happen to plasticity after secondary contact? | * What will happen to plasticity after secondary contact? | ||
| - | === Step 1: Genetic versus plastic divergence === | + | |
| + | ==== Divergence with gene-flow ==== | ||
| + | * Here, we will study speciation without an allopatric phase | ||
| + | * Nevertheless, | ||
| + | * ... and expression of plasticity may itself lead to a reduction in gene flow (plastic magic trait) | ||
| + | * Previous models: Gavrilets and Vose 2007, Thibert-Plante and Hendry 2011 | ||
| + | * We will follow these approaches by analyzing a model with the following ingredients: | ||
| + | * Two habitat types, connected by migration | ||
| + | * Plastic and genetic adaptation possible | ||
| + | * Ecological trait may influence mate choice | ||
| + | * Female preference and/or choosiness may evolve | ||
| + | * In contrast to Thibert-Plante and Hendry (2009), we will focus on scenarios that allow for the evolution of assortative mating | ||
| + | * Key questions: | ||
| + | * Interaction between plastic and genetic barriers to gene-flow | ||
| + | * Interaction between evolution of assortative mating and evolution of plasticity (e.g., AM might increase reliability of genetic cues, sensu Leimar et al. 2006) | ||
| + | * Methods: Population-genetics modeling, coupled with adaptive dynamics; stochastic individual-based simulations | ||
| + | === Old version: Genetic versus plastic divergence === | ||
| * The DPHS proposes that genetic divergence is preceded by the evolution of a purely plastic polyphenism. | * The DPHS proposes that genetic divergence is preceded by the evolution of a purely plastic polyphenism. | ||
| * This has a simple explanation if plasticity is the ancestral state of a lineage encountering a variable environment, | * This has a simple explanation if plasticity is the ancestral state of a lineage encountering a variable environment, | ||
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| * Are the results compatible with the predictions by Leimar et al. (2006)? | * Are the results compatible with the predictions by Leimar et al. (2006)? | ||
| - | === Step 2: Ecological plasticity and the evolution of reproductive isolation === | + | === Old version: Ecological plasticity and the evolution of reproductive isolation === |
| * The DPHS assumes plasticity in an ecological trait (an character conferring ecological adaptation). Our aim will be to study how such plasticity influences the evolution of prezygotic reproductive isolation. | * The DPHS assumes plasticity in an ecological trait (an character conferring ecological adaptation). Our aim will be to study how such plasticity influences the evolution of prezygotic reproductive isolation. | ||
| * To our knowledge, the only model on this subject is by Thibert-Plante and Hendry (2009). These authors assume ... Importantly, | * To our knowledge, the only model on this subject is by Thibert-Plante and Hendry (2009). These authors assume ... Importantly, | ||