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Abstract Although consumptive effects of predators have long been central to ecology, predation‐risk effects have emerged as major components of predator–prey interactions. Both consumptive and predation‐risk effects should vary with predator functional traits (e.g., hunting mode, gape size), where consumption rates and induction of morphological and behavioral defenses correlate with prey‐specific predator threat. Ambush predators, in contrast with active predators, may face selection pressure to be cryptic to avoid detection by prey. Thus, ambush predators may change prey density through consumptive effects but have reduced or absent predation‐risk effects. We performed two mesocosm experiments with free‐roaming and caged predators to explore post‐colonization interactions of the chemically camouflaged, large‐gaped, ambush predator, pirate perch (Aphredoderus sayanus), active, large‐gaped green sunfish (Lepomis cyanellus), and active, small‐gaped golden topminnow (Fundulus chrysotus), with larval gray treefrogs (Hyla chrysoscelis) and mole salamanders (Ambystoma talpoideum). We examined the consumptive and predation‐risk effects of each predator on amphibian mortality, growth rates, tail morphology, and polyphenisms. Large‐gaped pirate perch and green sunfish had strong, equivalent consumptive effects, but only the free‐roaming active predator, green sunfish, suppressed the growth of survivors through risk‐induced trait responses. Caged green sunfish induced much stronger non‐consumptive mortality than pirate perch in gray treefrogs, an effect that was absent for mole salamanders; golden topminnows had intermediate effects. Tail defenses were a function of prey mortality and only manifested in free‐roaming predator treatments, suggesting the necessity of predator attacks or conspecific alarm signals. Likewise, mole salamander polyphenism was unaffected by caged predators, whereas free‐roaming green sunfish prevented all metamorphosis. Free‐roaming golden topminnows increased the proportion of individuals remaining as larvae, and pirate perch increased the proportion of paedomorphs and metamorphs. Overall, the prey had positively correlated anti‐predator responses across life stages, suggesting multicomponent defenses. Predator effects varied with functional traits with large‐gaped predators having strong consumptive effects, but active predators causing stronger risk‐induced changes in growth compared to cryptic ambush predators, which provides more evidence for chemical camouflage. Our results emphasize the role of hunting mode and gape size in determining consumptive and predation‐risk effects, and that predation‐risk effects cannot be reliably predicted from consumptive effects. |
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