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Based on the same data, evidence for divergence in time to hatching was found between two of the populations [ 31].
Despite the divergence in time scales between the two phases, both types of transcriptome reorganization presented relationships between transcriptional fluctuations and the degree or magnitude of stress.
Molecular phylogenies are currently the best option to provide solid evidence on the origin, relationships and divergence in time among populations, particularly for organisms such as planarians, which are lacking reliable morphological characteristics.
In a first part of the paper, we fit a measure of backbone gene order conservation (hereinafter called backbone stability) against phylogenetic distance for over 3000 genome comparisons, improving existing models for the divergence in time of backbone stability.
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Henceforth, we shall call the locations of these shifts divergence points in time or phylogenetic trees.
We use lines artificially selected for divergence in development time, pupal mass or egg size, thus, exploiting the standing genetic variation in pre-adult traits present in natural populations of Bicyclus anynana.
This indicates a common ancestor, with a divergence in the time of SDH gene acquisition.
If parental species are adapted to different habitats in parapatry, divergence in flowering time can be reinforced in the contact zone, thereby preventing gene flow and maladaptive hybridization.
Allochronic separation (divergence in breeding times) can also result in non-random mating and contribute to increased genetic variance across the landscape [ 3].
Coalescence simulation will stop either when there remains a single lineage or when the simulated time is beyond the divergence (looking back in time).
In molecular clock calculations, using a model of sequence evolution that does not fully capture sequence saturation and among-site rate variation potentially can lead to large errors in divergence time estimates (reviewed in [ 3]).
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