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Rather, they reveal a genetic division into seven major groups.
This result is also supported by the STRUCTURE analysis showing that genetic division did not occur.
However, this genetic division and the lack of current gene flow remains perplexing given the relatively short distance between Hispaniola and Cuba (approximately 85 km).
Riginos [52] suggests that a Plio-Pleistocene mid-peninsular seaway is the simplest explanation for a concordant genetic division within both terrestrial and marine vertebrates.
The goal of the AMOVA was to identify the deepest genetic division in each gene.
Autosomal STR variation studies [ 27] revealed a pronounced genetic division between Polynesians and Western Austronesians.
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However, molecular studies have shown that there are deep genetic divisions in cultivated rice [12, 19] and that some of these divisions appear to extend back in time before rice was domesticated [41, 56, 79, 88].
The three major genetic divisions I to III identified by the phylogenetic analysis of concatenated sequences of nine housekeeping genes correspond to a large degree to those previously defined by analysis of recA, tly and camp5 sequences [21], [22], [38].
Deep genetic divisions were also observed in E. fallax.
Three major genetic divisions, known as types I, II, and III, are currently recognized.
This is in contrast to the deep genetic divisions reported for other montane species in Taiwan.
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