An important hypothesis concerning the role of aggregation in the antipreda
tor defense of aposematic insects is that a group projects a larger aposema
tic signal to a predator. The nearly exclusive use of birds as model predat
ors may be leading us to over-emphasize the importance of signal amplificat
ion as an explanation for the gregarious behavior of aposematic insects. Am
bush (sit-and-wait) predators such as amphibians and praying mantids make p
redatory decisions relying primarily on prey movement, and secondarily on p
rey size, with pre) color being less important. Therefore, we tested the in
teraction of aposematic coloration and gregarious behavior in insect defens
e from frogs. We offered frogs four types of mealworm prey: (1) cryptic and
solitary, (2) cryptic and gregarious, (3) aposematic and solitary, and (4)
aposematic and gregarious. The frogs ate aposematic and gregarious prey si
gnificantly later than they ate cryptic and gregarious prey and cryptic and
solitary prey. Our results support the hypothesis that aposematic colorati
on in gregarious prey, but not in solitary prey, can function to produce a
sufficient aposematic signal to delay attack by an ambush predator. This re
sult was not due to predator learning. Hence, the antipredator benefits of
aposematic coloration in aggregated prey may function in encounters with a
wide range of predators, including frogs.