Table 2.
FgenesposSel |
α |
|||
---|---|---|---|---|
Source | Estimate | Var. (%) | Estimate | Var. (%) |
(A) | ||||
Intercept | 0.0016∗∗∗ | 0.0217∗ | ||
π, intergenic regions | 0.5226∗∗∗ | 28.04 | 70.8561∗∗∗ | 62.72 |
Depth of sequencing | 1.9 ×10−5∗∗∗ | 17.08 | ||
(B) | ||||
Intercept | 0.0018∗∗∗ | 0.0335 | ||
log10 (census size) | 0.0000 | 0.81 | 0.0092 | 0.93 |
Mating system (selfing) | −0.0009∗ | 7.63 | −0.1086∗∗∗ | 17.57 |
Ancestral cluster (west) | −0.0004 | 5.93 | −0.0036 | 3.67 |
log10 (distance to core) | −0.0024∗∗ | 11.50 | −0.3292∗∗∗ | 34.36 |
Admixture (yes) | 0.0013∗∗ | 9.39 | 0.0837∗ | 2.36 |
Depth of sequencing | 2.1 ×10−5∗∗∗ | 16.63 |
The response variables are the fraction of genes with a significant McDonald–Kreitman test (FgenesposSel) and the rate of adaptation estimated on non-synonymous versus synonymous sites (α). FgenesposSel was influenced by the depth of sequencing, which was therefore included as a covariate. The sample size was 52 populations. Variance explained by genomic diversity (R2) was 0.28 and 0.63, respectively, for the two variables; variance explained by the model with demographic factors was 0.52 (including depth of sequencing) and 0.59, respectively. Estimated intercept and coefficients, and variation explained are reported. Significance is indicated: ∗0.01 < P ≤ 0.05, ∗∗0.001 < P ≤ 0.01, ∗∗∗P ≤ 0.001.