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During the first experiment, interactions of both osmotic potential and varieties were significant at all variables.
In the present experiment, interactions between developmental low-level methylmercury (MeHg) and nutritionally relevant dietary selenium (Se) on operant behavior and its persistence were examined in aged animals.
Models were not significantly improved by allowing λ and/or α to vary with experiment, interactions between experiment and infection, or replicate cages within experiments (see Appendix S1 for full details).
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In addition, a significant accession x experiment interaction (P = 1×10−5) was detected, suggesting that the reduction of plant growth due to CMV infection depended on the time of infection for each accession.
For all parameters measured there was no group times experiment interaction.
The only significant term involving spatial cueing and the Experiment factor was the three-way Cue Side × Hand Alignment × Experiment interaction [ F 1, 46) = 5.0, p =.03].
One other significant term that involved the factor Experiment was the Target Eccentricity × Hand Alignment × Experiment interaction [ F 1, 46) = 6.0, p =.02].
There was no significant genotype × experiment interaction effect, therefore, no change in the magnitude of the differences between genotypes across experiments was seen.
Of particular interest was the lesion by experiment interaction (F 1,16) = 15.7, P < 0.001), reflecting the selective poorer performance of the Hpc1 rats in the spatial biconditional learning task.
> The decrease in d′ was specific for the lip experiment (significant time × experiment interaction: F2,66 = 3.30, P < 0.05; no significant main effect of time in the hand experiment; Table 2, Fig. 3 A).
When we compare Experiments 1 and 2, it is evident that the experimental manipulation of color affected performance less than the manipulation of location [Manipulation × Experiment interaction: F 1, 16) = 22.6, p <.001].
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