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Previous comparative studies of development between C. elegans and P. pacificus have also demonstrated that sequence divergence is correlated with divergence in a number of developmental processes [ 8– 10].
Previous studies demonstrated significant divergence among serotypes A, B, C and D, which are thought to be haploid.
The expression levels among paralog gene pairs demonstrated clear divergence.
ITS-2 was more conserved among different strains of O. ophiodiicola but still demonstrated interspecific divergence.
In Africa, enhanced surveillance demonstrated significant divergence of CoVs in bats from Kenya (101).
These same maps demonstrated subgenome divergence as SSR primer pairs frequently generated amplicons for only some of the four subgenomes.
Haas et al. (2010) demonstrated morphological divergence of a stream fish in reservoirs using field-collected specimens.
In the rhinolophids, the host phylogram demonstrated genetic divergence between R. ferrumequinum and other species, as shown by the division of Rhinolophus bats into 2 groups.
Extended follow-up (cut-off 10 March 2010) demonstrated continued divergence of the survival curves (HR 0.72; 95% CI 0.61 0.84; P < 0.0001) [ 5].
The limited phylogenetic studies focusing on or including Arabian species have demonstrated concordant divergence timings for taxa with similar biogeographic origins [ 16– 20], however these biogeographic patterns remain largely understudied for most Arabian taxa.
The second of these was used in conjunction with the first in a phylogenetic analysis, which demonstrated evolutionary divergence of mammalian CBR enzymes from those of fungi and plants (Certik et al., 1999).
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