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Despite this evolutionary relationship, these two species differ greatly in genome size and gene expression patterns.
Despite this evolutionary complexity, saxitoxin is produced by members of two different kingdoms of life: cyanobacteria and dinoflagellates.
In turn, functional significance of certain features is implicated by preservation despite this evolutionary change; these features include tail-to-tail arrangements of HSEs, gapped HSEs, and the presence or absence of entire HSEs.
Despite this evolutionary significance, their phylogenetic relationships are understudied.
Yet despite this evolutionary flux there seems to be a strong purifying selection across all intact genes.
Despite this evolutionary conservation of gene families, lineage-specific fluctuations in gene family size are frequent among taxa [ 41, 43].
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Despite this potential evolutionary dead-end, the limited or even absent gene flow between supercolonies of unicolonial ant species [2], [8], [9], [10] may be conducive to speciation [22].
Despite this reconciliation, evolutionary biologists still have great difficulty in recognizing species in the early stages of divergence due to the limited time for differences to evolve that satisfy most delimitation criteria [5].
Despite this uncertainty, evolutionary sequence conservation is considered a reliable indicator of biological activity [ 49], and several noncoding ECRs were validated as enhancers [ 13, 38, 41, 49, 50].
Despite this, the evolutionary history of reproductive systems in Notostraca is unknown due to the lack of a resolved phylogeny [ 33, 34], and the poor knowledge of the diversity of the group, partly due to the widespread presence of cryptic species [ 32, 35- 38].
This occurs despite the evolutionary distance, an ∼25% smaller catalytic domain, and an increase in Ea of ∼11 kcal/mol.
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