Life Cycle Complexity Influences Intraguild Predation and Cannibalism in Pond Communities
Predation risk is an important contributor to community structure that varies in response to abiotic and biotic factors. In aquatic habitats, predation risk is often linked to hydroperiod as the latter directly influences predator identity within these ecosystems. For pond-breeding salamanders, intraguild predation (IGP) and cannibalism are prevalent interactions in larval communities, but the frequency of each type of agonistic interaction, as well as changes in their pervasiveness along hydroperiod gradients are not well understood. Size-structured populations of aquatic life stages (paedomorphic adults and overwintered larvae) of mole salamanders (Ambystoma talpoideum) have the potential to be dominant IG predators and cannibals in permanent ponds because of large size advantages over successive cohorts, but the species exists as only a single larval cohort in temporary ponds with reduced predatory abilities on guild members. Thus, both the potential for and intensity of predation by this species is linked to hydroperiod; yet, the predatory abilities of aquatic life stages of mole salamanders have not been evaluated. This study examined the extent to which larger size classes (paedomorphs and overwintered larvae) of mole salamanders preyed upon conspecifics and a congeneric competitor, the spotted salamander (Ambystoma maculatum). Predation trials occurred in indoor microcosms and were executed under two habitat treatments that included pseudo-natural conditions containing alternate prey and refugia, as well as simplified environments (no alternative food or cover). Embryos or hatchlings of mole and spotted salamanders were exposed either separately or concurrently to paedomorphic and overwintered larval mole salamanders in each habitat treatment. Additionally, overwintered larvae were offered as prey to paedomorphic adults. No significant differences in mortality were observed between habitat treatments (complex versus simple) for either embryo or hatchling predation experiments. Mortality of mole and spotted embryos did not differ when they were offered separately or together, but paedomorphs caused significantly higher mortality among mole embryos compared to spotted embryos. Hatchlings of both species were heavily preyed upon (nearly 100% in all trials), but overwintered larvae exhibited 100% survival with paedomorph predators, indicating size-thresholds of predation risk that were not species specific. Paedomorphs and overwintered larvae therefore are most likely generalist predators that feed equally and effectively on hatchlings of co-occurring species, but are more likely to consume egg masses that do not incur significant handling costs. When present, paedomorphs or overwintered larvae have the potential to alter population dynamics of both guild members and conspecifics by being dominant predators on early life stages. As the prevalence of overwintering and paedomorphosis varies along hydroperiod gradients, predation risk from this species is likely to occur discontinuously and thereby may be an important, yet variable, structuring force.

Variation in the life cycle of Ambystoma talpoideum along a hydroperiod gradient, which changes their trophic position. The left diagram demonstrates facultative paedomorphosis, including potential outcomes of overwintered larvae and paedomorphs, which can occur in ponds of semi-permanent to permanent hydroperiod. The right diagram shows the life cycle of non-paedomorphic populations of mole salamanders that undergo obligate metamorphosis, the only possible scenario in ephemeral ponds. The right diagram is also representative of some congeneric pond-breeding species, such as A. maculatum. Dashed boxes represent life history stages that potentially overlap in increasingly permanent ponds, creating size-structured populations, and are the stages used in the current study. Cartoon salamanders represent where 1) paedomorphs, 2) overwintered larvae, and 3) larvae in non-overlapping age cohorts are predicted to exist along hydroperiod and trophic level gradients.

Mean embryonic mortality (±SE) of Ambystoma talpoideum (Mole) and A. maculatum (Spotted) by paedomorphic mole salamanders in “complex” and “simple” conditions. “Mixed” treatment included egg masses of both species simultaneously, and “Mole Only” and “Spotted Only” had only that species' embryos present.

Mean mortality (±SE) of hatchling and larval mole (A. talpoideum), and hatchling spotted (A. maculatum) salamanders in the “complex” treatment. Predators are indicated in the top row, and prey in the bottom row of the x-axis, respectively, except for control treatments where one size class was used. No bar exists for Paedomorph-OW Larvae (overwintered larvae) and OW Larvae Control treatments as 100% survival occurred. No error bars exist in the OW Larvae-Hatchling treatment due to 100% mortality.

Relationship of prey mortality with prey to predator size difference using a generalized additive model. Dashed trendline indicates smoothed estimation of prey mortality (%) using regression splines (adj. r2 = 0.97, P < 0.001). Predator–prey size differences were calculated as (predator SVL–prey SVL)/predator SVL.

Mean mortality (±SE) of hatchling mole (A. talpoideum) and spotted (A. maculatum) salamanders when offered simultaneously to paedomorphic mole salamander predators.
Contributor Notes
Associate Editor: M. J. Lannoo.