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. 2023 Nov 2;36(12):1796–1810. doi: 10.1111/jeb.14241

TABLE 3.

Estimated variance components and derived parameters for the six models of performance in the detour task trials.

Parameter Model
A1 null model A2 phenotypic model A3 IxE model A4 animal model A5 full GxE model A6 animal model with PxE
V B 0.018 (0.013) 0.016 (0.014) 0.015 (0.013) 0.016 (0.014) 0.013 (0.01) 0.015 (0.013)
V BT 0.013 (0.012) 0.000 (−) 0.000 (−) 0.000 (−) 0.000 (−) 0.000 (−)
V R 0.730 (0.032) 0.392 (0.021) 0.392 (0.021) 0.392 (0.021) 0.392 (0.021) 0.392 (0.021)
V I 0.357 (0.038)

0.372 (0.056)1

0.343 (0.052)2

V A 0.000 (−)

0.253 (0.140)1

0.000 (−)2

0.000 (−)
V PE 0.357 (0.038)

0.174 (0.092)1

0.336 (0.051)2

0.371 (0.056)1

0.343 (0.051)2

r G −0.999 (−)
R 0.467 (0.033)

0.477 (0.043)1

0.458 (0.042)2

h 2 0.000 (−)

0.304 (0.146)1

0.000 (−)2

0.000 (−)
pe2 0.467 (0.033)

0.209 (0.119)1

0.454 (0.042)2

0.477 (0.043)1

0.458 (0.042)2

Note: Subscripts denote block (B), brood tank (BT), residual (R), individual (I), permanent environment (PE) and additive genetic (A) components of variance. Also shown, where applicable are corresponding estimates of repeatability (R), heritability (h 2), the intraclass correlation corresponding to V PE (denoted pe2) and the cross‐treatment genetic correlation (r G). Parameter estimates specific to treatment 1 (clear cylinder) and 2 (marked cylinder) are denoted with subscripts and associated standard errors from each model are provided in parentheses where available. Note that variances were constrained to be positive and correlations between −1 and +1. Where parameters are fixed at boundary conditions no SE is estimated.