In paired-choice assays, two treatments are presented simultaneously t
o each subject. Data from such arrays should not be considered to be i
ndependent, and correct statistical-analysis must account for the corr
elation. A statistical test that often is appropriate for these assays
is the paired-sample t-test. I present curves showing the extent to w
hich statistical power of this test is affected by sample size, effect
size (i.e., magnitude of treatment differences), and correlation. For
a given effect size and replication, positive correlation between pai
red observations substantially improves power of the test, whereas neg
ative correlation reduces power. I conducted a literature sun ev of pa
ired-choice assays to determine whether there are patterns in effect s
izes and correlation that might assist in designing studies or in pred
icting minimum sample sizes necessary to achieve reasonable statistica
l power; experiments were categorized according to whether they were f
eeding or oviposition assays. The review indicated that correlation wa
s highly variable and ranged between strongly negative and strongly po
sitive values. Oviposition assays showed larger positive correlations
than did feeding assays, resulting in larger effect sizes (adjusted fo
r correlation); however, feeding assays tended to use larger sample si
zes than oviposition assays, hence estimated statistical power was sim
ilar between the two types of assays. Oviposition assays often used mu
ltiple insects per arena, apparently sacrificing replication, whereas
feeding assays tended to use a single insect per arena. Approximately
45% of experiments failed to detect significant treatment effects. The
majority of nonsignificant assays had too few replications to detect
even a large effect size with a reasonable statistical power. Literatu
re examples are presented to show that assay methodology (specifically
number of insects per arena, distance between paired choices, and ass
ay duration) can affect correlation, effect size, and statistical powe
r. Finally, scatter plots of Che data, although rarely presented, are
shown to provide insight into methodological, statistical, and biologi
cal aspects of paired-choice assays.