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We argue that the discrepancy can be explained by the difference in experiment designs between the two studies.
With regard to distal subiculum there was significant higher PHC than PRC connectivity in Experiment 1 (t(14) = 3.1, p = 0.009) and a trend towards a difference in Experiment 2 (t(13) = 2.0; p = 0.063).
This latency difference in Experiment 2 was then carried over into the very beginning of active training in Experiment 2B, but rapidly disappeared with repeated swims in the pool.
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From Fig. 2 it is clear that there are no significant differences in experiment 1 (synchronous condition, counsellor is Self or Freud) for MeDown, MeMirror and MyMovements.
Anyhow, there were no significant differences in experiment indexes between the shrimp fed the FMN and FMR diets, nor between the shrimp fed the SBR and SBRR diets.
Circumstances such as differences in experiment designs and analytical platforms may be causative of this discrepancy.
The group differences in Experiment 2 are consistent with the strong positive correlation that appearance schematicity demonstrates with other body image variables [e.g., thin internalisation, [ 31].
The results of Experiment 6 were highly similar to those of Experiment 5, ruling out flicker rate as a possible explanation for the observed search differences in Experiment 1 (Fig. 8).
(As the group of baboons was transferred to another facility, we could not test them in this condition, but they had successfully discriminated 60%% size differences in Experiment 1).
Disparity in the various studies is ascribed to differences in experiment design, including type of fatty acid substrates, concentrations of fatty acids, incubation times, contents of medium (nutritional substrates), stages of differentiation, and culture condition (growth supports).
(The same 95% percentile value for 2 experiments with different number of participants is explained by larger number of zeros [absence of a significant difference] in Experiment 2, probably because of smaller difference between ARs).
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