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Table 4 Geographic variation in natural selection acting on camellia pericarp thickness.

From: Natural selection drives the fine-scale divergence of a coevolutionary arms race involving a long-mouthed weevil and its obligate host plant

  

Pericarp thickness (β σ )

DBH

Locality

Opportunity for

selection

Coef.

SE

t

P

Coef.

SE

t

P

Fukagawa (FK)

0.459

0.074

0.119

0.6

0.5380

- 0.024

0.119

-0.2

0.8420

Shiratani (SR)

1.305

0.524

0.188

2.8

0.0089*

0.141

0.188

0.8

0.4566

Kawahara (KW)

1.998

- 0.070

0.147

- 0.5

0.6340

0.660

0.147

4.5

< 0.0001*

Ohko-rindoh (OK)

2.764

0.669

0.277

2.4

0.0218

0.136

0.277

0.5

0.6265

  1. The number of surviving seeds, which was converted into relative fitness, was regressed on the pericarp thickness of camellia trees for each population. The effect of tree sizes on the number of seeds was controlled for by incorporating diameter at breast height (DBH) into a generalized linear model (i.e. multiple regression on pericarp thickness and DBH). Both explanatory variables were z-standardized (zero-mean, unit-variance) before regression. Thus, the partial regression coefficient for pericarp thickness represents standardized linear selection coefficient (i.e. β σ ). The opportunity for selection (i.e. the variance of relative fitness) is also shown. See additional file 2 for the results of quadratic regression analyses.
  2. *Significant after sequential Bonferroni correction, which was applied for each column (i.e. explanatory variable) (α = 0.05).