In some cases, finding divergence in neutral DNA in morphologically divergent subspecies depends on the type of marker used [32].
Based on preliminary analysis of selected taxa of Parthenium, the central region of the matK gene was the best for finding divergence in Parthenium species.
Hence in this study, similar to Demirel and Anbarjafari's study [6, 8], we use KLD as a metric for finding the divergence between the PDFs.
Due to the lack of information about the magnetic flux on cell faces, the problem of finding such divergence-preserving prolongation operators becomes underdetermined.
Our results obtained from a multiple-model approach in general echo Sosnaud et al.'s (2013) finding that divergence between subjective and objective social status is shaped in a sociologically meaningful way.
However, these estimates still differ substantially from one another with some finding this divergence to be in the Lower Cretaceous [22], [68] and others in the Late Triassic or Early Jurassic [19], [33].
We investigated the compositional differences in a set of 774 sequenced microbial genomes, finding rapid divergence among closely related genomes, but also convergence of compositional patterns among genomes with similar habitats.
Using only arthropod fossil calibrations, our molecular clock analyses support earlier studies that used vertebrate calibrations in finding a deep divergence of deuterostomes and arthropods, hundreds of millions of years before the Cambrian explosion.
The methodology developed for joining cliques is powerful for finding the commonalities and divergences among populations with respect to their gene signatures.
After finding that many deep divergences remained weakly supported, we sequenced eleven additional genes (6,375 bp) for a 27-taxon subset.
