2008
DOI: 10.1098/rspb.2008.0882
|View full text |Cite
|
Sign up to set email alerts
|

Incipient allochronic speciation due to non-selective assortative mating by flowering time, mutation and genetic drift

Abstract: We model the evolution of flowering time using a multilocus quantitative genetic model with non-selective assortative mating and mutation to investigate incipient allochronic speciation in a finite population. For quantitative characters with evolutionary parameters satisfying empirical observations and two approximate inequalities that we derived, disjunct clusters in the population flowering phenology originated within a few thousand generations in the absence of disruptive natural or sexual selection. Our s… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1
1

Citation Types

5
109
0

Year Published

2010
2010
2022
2022

Publication Types

Select...
8
1
1

Relationship

0
10

Authors

Journals

citations
Cited by 65 publications
(114 citation statements)
references
References 80 publications
5
109
0
Order By: Relevance
“…Strong assortative mating produces high correlations of allelic effects among all loci, which leads to the evolution of two phenotypic classes: one with alleles increasing the trait and the other with alleles decreasing the trait (Crow and Kimura, 1970). Devaux and Lande (2008) found similar results using a finite diploid population with multiple alleles per locus and they showed that the splitting of the phenotype distribution is possible under strong assortative mating and genetic drift, but the distribution is transient rather than permanent. However, our distribution is not transient, and this is probably because we only considered two allelic states for each locus.…”
Section: Evolution Of Quantitative Trait Distributionsupporting
confidence: 64%
“…Strong assortative mating produces high correlations of allelic effects among all loci, which leads to the evolution of two phenotypic classes: one with alleles increasing the trait and the other with alleles decreasing the trait (Crow and Kimura, 1970). Devaux and Lande (2008) found similar results using a finite diploid population with multiple alleles per locus and they showed that the splitting of the phenotype distribution is possible under strong assortative mating and genetic drift, but the distribution is transient rather than permanent. However, our distribution is not transient, and this is probably because we only considered two allelic states for each locus.…”
Section: Evolution Of Quantitative Trait Distributionsupporting
confidence: 64%
“…Because this need not require geographical isolation, allochronic speciation is often considered a special case of sympatric speciation (Alexander and Bigelow 1960;Yamamoto and Sota 2009). Evidence for allochronic speciation exists for organisms such as insects, fish, and plants (Alexander and Bigelow 1960;Simon et al 2000;Ritchie 2001;Devaux and Lande 2008;Yamamoto and Sota 2009). For birds and other tetrapods, we are aware of only one example of allochronic speciation, which involves sympatric seabirds (Friesen et al 2007).…”
Section: Discussionmentioning
confidence: 99%
“…Adaptive change is facilitated when the trait under selection is also the trait according to which individuals choose mates (Doebeli & Dieckmann 2000;but see Fox 2003). For a trait such as timing of breeding, some level of assortative mating between individuals with similar trait values is inevitable (Fox 2003;Weis & Kossler 2004;Weis 2005), and the resulting inflation of genetic variance can hasten evolutionary change in breeding time (Hendry & Day 2005;Devaux & Lande 2008).…”
Section: Evolution Of Phenologymentioning
confidence: 99%