Table 3 |
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|
P450 genotype and allele frequencies in a cold selection environment |
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|
Genotype frequency Observed (Expected) |
Allele frequency |
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|
|
|
||||||||
|
Cross |
Gen. |
SS |
RS |
RR |
S |
R |
na |
HWEb |
Driftb |
|
|
|
|
|
|
|
|
|
|
|
|
A #1 |
F2 |
0.25 |
0.50 |
0.25 |
0.50 |
0.50 |
|||
|
F4 |
0.46 (0.53) |
0.54 (0.39) |
0 (0.08) |
0.73 |
0.27 |
280 |
<0.0001* |
<0.0001* |
|
|
F8 |
0.26 (0.38) |
0.71 (0.47) |
0.03 (0.15) |
0.62 |
0.38 |
920 |
<0.0001* |
0.0066 |
|
|
F12 |
0.32 (0.44) |
0.68 (0.45) |
0 (0.11) |
0.66 |
0.34 |
160 |
<0.0001* |
0.1841 |
|
|
A #2 |
F2 |
0.25 |
0.50 |
0.25 |
0.50 |
0.50 |
|||
|
F4 |
0.21 (0.21) |
0.49 (0.49) |
0.30 (0.30) |
0.46 |
0.54 |
310 |
0.8320 |
0.1068 |
|
|
F8 |
0.04 (0.17) |
0.73 (0.48) |
0.23 (0.35) |
0.41 |
0.59 |
1280 |
<0.0001* |
0.1716 |
|
|
F12 |
0 (0.17) |
0.84 (0.49) |
0.16 (0.34) |
0.42 |
0.58 |
1040 |
<0.0001* |
0.3875 |
|
|
B #1 |
F2 |
0.25 |
0.50 |
0.25 |
0.50 |
0.50 |
|||
|
F4 |
0.12 (0.22) |
0.70 (0.50) |
0.18 (0.28) |
0.47 |
0.53 |
140 |
<0.0001* |
0.2041 |
|
|
F8 |
0.07 (0.28) |
0.86 (0.50) |
0.04 (0.22) |
0.53 |
0.47 |
1160 |
<0.0001* |
0.1204 |
|
|
F12 |
0.27 (0.39) |
0.71 (0.47) |
0.02 (0.14) |
0.63 |
0.37 |
560 |
<0.0001* |
0.0284 |
|
|
B #2 |
F2 |
0.50 |
0.25 |
0.25 |
0.50 |
0.50 |
|||
|
F4 |
0.45 (0.50) |
0.52 (0.41) |
0.03 (0.09) |
0.71 |
0.29 |
270 |
<0.0001* |
<0.0001* |
|
|
F8 |
0.19 (0.27) |
0.66 (0.50) |
0.15 (0.23) |
0.52 |
0.48 |
840 |
<0.0001* |
<0.0001* |
|
|
F12 |
0.23 (0.36) |
0.74 (0.48) |
0.03 (0.16) |
0.60 |
0.40 |
800 |
<0.0001* |
0.0529 |
|
|
|
|||||||||
|
a total number of 4th instar larvae used in genotype monitoring assay b Nominal p-values are reported for the probability that the data fit the null hypothesis of Hardy-Weinberg equilibrium (or genetic drift) * indicates tests that remain statistically significant after Bonferonni correction over the entire experiment |
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|
Hardstone et al. BMC Evolutionary Biology 2009 9:42 doi:10.1186/1471-2148-9-42 |
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