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. 2014 Mar 20;7(4):506–518. doi: 10.1111/eva.12154

Table 1.

Evaluation of alternative models for genetic parameters based on population size and isolation variables.

Models with D.centre
Models with D.near
N.pop Area D.centre Area + D.centre Area*D.centre N.pop Area D.near Area + D.near Area*D.near
He
AICc −91.9 −85.9 −99.6 −103.6 115.6 91.9 −85.9 −87.3 −89.8 −89.1
ΔAICc 23.8 29.7 16.0 12.0 0.0 0.0 5.9 4.5 2.1 2.7
wi 0.0 0.0 0.0 0.0 1.0 0.6 0.0 0.1 0.2 0.1
FIS
AICc −63.2 −64.2 −63.0 −61.8 79.0 −63.2 −64.2 −63.2 −62.1 69.2
ΔAICc 15.7 14.8 16.0 17.2 0.0 6.0 5.0 6.0 7.1 0.0
wi 0.0 0.0 0.0 0.0 1.0 0.0 0.1 0.0 0.0 0.8
F
AICc −123.0 −119.5 139.5 −137.1 −134.6 123.0 −119.5 −121.9 −120.0 −117.0
ΔAICc 9.5 20.0 0.0 2.4 4.9 0.0 10.5 8.1 10.5 13.0
wi 0.0 0.0 0.7 0.2 0.1 1.0 0.0 0.0 0.0 0.0
DST
AICc −133.2 −127.4 145.8 −143.4 −141.1 133.6 −127.4 133.4 −131.0 −129.0
ΔAICc 12.6 18.5 0.0 2.4 4.7 0.2 6.0 0.0 2.4 4.4
wi 0.0 0.0 0.7 0.2 0.1 0.4 0.0 0.4 0.1 0.0

Genetic parameters: He = expected heterozygosity, inbreeding (FIS), accumulated inbreeding (F) and differentiation (DST). Model selection repeated for two alternative measures of isolation: distance to the centroid of all populations (D.centre) and distance to the nearest population (D.near). N.pop = male territories, Area = patch size. Additive (+) and interactive (*) effects were considered. The corrected Akaike information criterion (AICc), difference with the best model (ΔAICc) and the relative weight of evidence for each model (wi) are reported (two equally good models when wi < 0.5). Statistics of the most parsimonious model are highlighted in bold.