Exact(10)
For E. ivorense and E. suaveolens sequences, we used a single sample per major gene pool.
The chloroplast genome was globally congruent with the nSSRs data in terms of haplotype distribution because each major gene pool generally carried private haplotypes.
However a significant comparison was found within a major gene pool (Iw- Is), as well between two major gene pools in the LGR (Is- SCs).
Examination of the distribution of pDNA lineages in each major gene pool reveals some additional incongruences because even the haplotypes unique to SW are paraphyletic.
We used a two-step approach to identify (i) major gene pools showing no or negligible introgression (sharp boundaries) and (ii) minor gene pools displaying introgression (diffuse boundaries) within each major gene pool.
Within the major gene pool SC, the parapatric SCn and SCs shared many haplotypes from the second clade, but with higher haplotype diversity in SCs (12 haplotypes) than in SCn (6 haplotypes), despite a larger sample size in the later.
Similar(50)
We demonstrate the existence of two major gene pools in Central Europe and Northern America.
Hence, we considered that K = 3 is the optimal solution for identifying major gene pools.
The three major gene pools are found in different habitats and climatic conditions.
These two major gene pools are constructed from different taxonomic units.
It suggests that individuals from the major gene pools might hybridize on rare occasion.
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