Table II.
Secondary Trait | Figure | Sex | High-Active line | Control line | p-value | h2 | F | n | 95% CI | Dy | h2Reference | |
---|---|---|---|---|---|---|---|---|---|---|---|---|
Body mass (g)a | 2C | Male | 23.48 (±0.44) | 27.53 (±0.87) | <0.0001 | 0.37 | 0.06217 | 24 | 1.00 | −1.08 |
Falconer, 1973 (Table 5) |
|
Female | 18.58 (±0.29) | 22.32 (±0.77) | <0.0001 | 0.37 | 0.06217 | 24 | 1.00 | −1.35 | ||||
Gen 10 Cohort Home Cage Activity (km/day) |
3A | Male | 1.10 (±0.20) | 0.31 (±0.05) | 0.002 | 0.33 | 0.06217 | 24 | 0.98 | 1.68 |
Zombeck et al., 2011 (Table 1) |
|
Female | 1.83 (±0.28) | 0.34 (±0.05) | <0.0001 | 0.33 | 0.06217 | 24 | 0.98 | 2.35 | ||||
Wheel running (km/day) | 3B | Male | 8.34 (±0.73) | 4.90 (±0.62) | 0.002 | 0.39 | 0.06217 | 24 | 1.01 | 0.57 |
Zombeck et al., 2011 (Figure 6C) |
|
Female | 9.79 (±1.40) | 9.30 (±0.83) | NS | 0.39 | 0.06217 | 24 | 1.01 | 0.14 | ||||
Open Field (m) | 3C | Male | 45.88 (±4.41) | 27.14 (±2.72) | 0.003 | 0.13 | 0.06217 | 24 | 0.87 | 0.55 | DeFries et al., 1970 | |
Female | 37.65 (±2.60) | 29.12 (±4.01) | NS | 0.13 | 0.06217 | 24 | 0.87 | 0.80 | ||||
Rotarod (s)b | 3D | Male | 49.06 (±4.09) | 50.54 (±3.55) | NS | 0.44 | 0.06217 | 24 | 1.03 | −0.04 |
Rustay et al., 2003 Belknap et al., 1993 |
|
3E | Female | 39.28 (±3.83) | 58.56 (±8.95) | 0.026 | 0.44 | 0.06217 | 24 | 1.03 | −0.89 | |||
Response to 0.25 mg/kg Amphetamine (m/90 min)c Collapsed (test) |
4A+B | Male | −43.42 (±22.74) | 61.82 (±26.29) | 0.023 | 0.21 | 0.06217 | 22 | 0.95 | −2.18 | Alexander et al., 1996 | |
4C+D | Female | −84.55 (±31.02) | 27.84 (±17.47) | 0.02 | 0.21 | 0.06217 | 22 | 0.95 | −2.23 | |||
Response to 0.5 mg/kg Amphetamine (m/90 min)c Collapsed (test) |
4A+B | Male | −1.20 (±28.57) | 16.24 (±7.50) | NS | 0.21 | 0.06217 | 22 | 0.95 | −1.64 | Alexander et al., 1996 | |
4C+D | Female | −53.78 (±17.46) | 27.42 (±8.89) | 0.006 | 0.21 | 0.06217 | 22 | 0.95 | −2.93 | |||
Response to 2 mg/kg Amphetamine (m/90 min)c Collapsed (test) |
4A+B | Male | 70.43 (±41.36) | 64.94 (±21.31) | NS | 0.21 | 0.06217 | 22 | 0.95 | 0.09 | Alexander et al., 1996 | |
4C+D | Female | 58.13 (±58.16) | 59.33 (±17.73) | NS | 0.21 | 0.06217 | 22 | 0.95 | −0.02 | |||
Morris water maze latency (m) |
6 |
Galsworthy et al., 2005 (Table 4) |
||||||||||
Day 1 | Collapsed (sex, dose) |
10.64 (±0.64) | 11.74 (±1.05) | NS | 0.24 | 0.06217 | 0.96 | −0.28 | ||||
Day 2 | Collapsed (sex, dose) |
9.36 (±0.92) | 5.09 (±0.63) | 0.001 | 0.24 | 0.06217 | 22 | 0.96 | 1.21 | |||
Day 3 | Collapsed (sex, dose) |
6.21 (±0.92) | 3.50 (±0.53) | 0.015 | 0.24 | 0.06217 | 22 | 0.96 | 0.80 | |||
Day 4 | Collapsed (sex, dose) |
5.48 (±0.81) | 4.26 (±0.71) | NS | 0.24 | 0.06217 | 22 | 0.96 | 0.36 | |||
Day 5 | Collapsed (sex, dose) |
3.97 (±0.84) | 3.50 (±0.52) | NS | 0.24 | 0.06217 | 22 | 0.96 | 0.15 | |||
Total number of new cells in dentate gyrus (# BrdU+ cells)d |
7B | Male | 5313.02 (±421.51) | 4173.35 (±588.72) | NS | 0.53 | 0.06217 | 22 | 1.10 | 0.27 | Clark et al., 2011 | |
Female | 7592.58 (±758.05) | 5787.87 (±684.44) | 0.045 | 0.53 | 0.06127 | 22 | 1.10 | 0.59 |
Body Mass refers to Generation 10.
Rotarod refers to average latency of the 4 trials per day over three days.
Locomotor response to amphetamine expressed as a difference score relative to the saline group of each sex and line.
Total number of new cells in dentate gyrus refers to average total number of BrdU cells in the granule layer of the dentate gyrus collapsed across dose.
Standard errors are shown in parentheses next to means for the secondary phenotypic traits under “High-Active line” and “Control line”. “P-value” refers to a pair-wise comparison of the High-Active line versus the Control line. “F” refers to the inbreeding coefficient estimated from the entire pedigree. “n” refers to the number of families represented for the specific phenotypic trait that was analyzed. “95% CI” refers to the 95% confidence interval for Dy expected by genetic drift as calculated from equation 1 in the text. “Dy” refers to the difference between lines in standardized phenotypic units.
Dy values larger than the 95% CI are shown in bold and provide evidence that the secondary trait has evolved as a correlated response to selection for home cage activity.