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Exact(7)
In the Rhinolophus case, divergence between acoustic morphs may lead to both assortative mating and selection for divergent resource preferences.
However, in the case divergence dates are available for nodes of the species tree, the problem becomes amenable [ 2, 16].
This was found not to be the case (divergence time estimates differed by no more than 0.0005).
In either case, divergence times younger than ~20 Mya are unlikely to be biologically realistic and, therefore, provide a validation criterion for the accuracy of time estimates.
In Pseudo-nitzschia the degree of differentiation between strains was similar for ITS2 and ITS1, although in at least one case divergence in ITS1 sequences was more marked than that in ITS2 [ 34].
In this case, divergence between closely related species is determined by competition between gene flow and genetic drift, where the first tends to decrease divergence, and the latter to increase it [ 2].
Similar(53)
In contrast to the traditional LDA, MMDA attempts to find a low-dimensional subspace by maximizing the minimal (worst-case) divergence among classes.
In some cases, divergence dating in these studies were supported by dated fossil records.
In some cases divergence from the guideline is possible or even essential.
Our data suggest that in some cases divergence can also be promoted through sexual dimorphism in ecologically relevant characters.
In most cases, divergence in paralog assignment is already apparent at the immediate phylogenetic point of the duplication event (at the phylogenetic resolution of this study).
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