Consumption of the eggs, hatchlings, and tadpoles of Green Frogs (Lithobates clamitans) by native and non-native predators

Predation by native and non-native predators on the eggs, embryos, and early stage tadpoles can affect the recruitment of offspring into a population. We examined the effects of native (Little Brown Mudbugs, Cambarus thomai; overwintered Rana tadpoles; Common Green Darner, Anax junius, larvae) and non-native (Western Mosquitofish, Gambusia affinis) potential predators on the eggs, hatchlings, and early tadpoles of the Green Frog (Lithobates clamitans). The predators had no effect on survivorship or hatching of L. clamitans eggs. However, tadpole survivorship was significantly reduced by dragonfly larvae and crayfish, but not G. affinis or the overwintered ranid tadpoles. Our observation that invertebrates consumed Green Frog tadpoles while vertebrates did not is consistent with palatability contributing to the tadpoles’ susceptibility to different predators. Our results therefore suggest Green Frog tadpoles, but not eggs or embryos, from some populations may be subject to differential predation by invertebrate and vertebrate predators.

On dangerous ground: the evolution of body armour in cordyline lizards

Animal body armour is often considered an adaptation that protects prey against predatory attacks, yet comparative studies that link the diversification of these allegedly protective coverings to differential predation risk or pressure are scarce. Here, we examine the evolution of body armour, including spines and osteoderms, in Cordylinae, a radiation of southern African lizards. Using phylogenetic comparative methods, we attempt to identify the ecological and environmental correlates of body armour that may hint at the selective pressures responsible for defensive trait diversification. Our results show that species inhabiting arid environments are more likely to possess elaborated body armour, specifically osteoderms. We did not find any effect of estimated predation pressure or risk on the degree of body armour. These findings suggest that body armour might not necessarily evolve in response to direct interactions with predators, but rather as a result of increased habitat-mediated predation risk. Furthermore, we discuss the possibility that osteoderms might have been shaped by factors unrelated to predation.

Heterochrony in the evolution of Trinidadian guppy offspring size: maturation along a uniform ontogenetic trajectory

The size and maturity of Trinidadian guppy ( Poecilia reticulata ) offspring vary among populations adapted to environments of differential predation. Guppy offspring born to low-predation, high-competition environments are larger and more mature than their high-predation ancestors. Here we ask: what specific changes in developmental or birth timing occur to produce the larger, more mature neonates? We collected specimens across the perinatal window of development from five populations and quantified musculoskeletal maturation. We found that all populations undergo similar ontogenetic trajectories in skeletal and muscle acquisition; the only difference among populations is when neonates emerge along the trajectory. The smallest neonates are born with 20% of their skeleton ossified, whereas the largest neonates are born with over 70% of their skeleton ossified. The area of the major jaw-closing muscle is relatively larger in larger offspring, scaling with length as L 2.5 . The size range over which offspring are birthed among populations sits along the steepest part of the size–maturity relationship, which provides a large marginal increase in fitness for the high-competition female. Because of the functional effects of producing more mature offspring at birth, offspring size may be the first and most critical life-history trait selected upon in highly competitive environments.

Sex-specific predation risk and the evolution of sexual dimorphism in immunocompetence: a theoretical analysis

Sexual dimorphism in immunocompetence, with males having lower immune function, is a prevalent pattern in nature. The main evolutionary explanation for this pattern is that males preferentially allocate resources away from immune function and towards reproductive effort to increase their competitiveness for limited females. However, the role of differential predation risk between the sexes has not been considered, despite predation risk being a major driver of life history strategies and male sexual traits often having associated predation costs. It is unclear whether increased predation risk should increase or decrease investment in immune function, as males have been shown to utilize both behavioural (e.g. decrease foraging activity) and/or life-history (e.g. decrease investment in sexual trait) defense strategies to manage predation risk. Here, we modelled optimal resource acquisition and allocation towards immune function under differential predation risk with multiple defense strategies. If males have limited defense strategies, increasing predation risk caused males to trade-off immune function for reproductive effort, leading to reduced immunocompetence. In contrast, if males can only decrease predation risk through reduction of reproductive effort (e.g. decrease colouration or calling rates), then increasing predation risk causes immune function to increase. If males can utilize multiple defense strategies and sexual selection is low, then males maintain a constant immune function as predation risk increases. Sexual selection robustly resulted in decreased immunocompetence. Overall, our results suggest that predation plays an important role in the evolution of sexual dimorphism in immunocompetence, but predicting its effect requires understanding the integrated defense strategies available.

Sex-specific predation risk and the evolution of sexual dimorphism in immunocompetence: a theoretical analysis

Sexual dimorphism in immunocompetence, with males having lower immune function, is a prevalent pattern in nature. The main evolutionary explanation for this pattern is that males preferentially allocate resources away from immune function and towards reproductive effort to increase their competitiveness for limited females. However, the role of differential predation risk between the sexes has not been considered, despite predation risk being a major driver of life history strategies and male sexual traits often having associated predation costs. It is unclear whether increased predation risk should increase or decrease investment in immune function, as males have been shown to utilize both behavioural (e.g. decrease foraging activity) and/or life-history (e.g. decrease investment in sexual trait) defense strategies to manage predation risk. Here, we modelled optimal resource acquisition and allocation towards immune function under differential predation risk with multiple defense strategies. If males have limited defense strategies, increasing predation risk caused males to trade-off immune function for reproductive effort, leading to reduced immunocompetence. In contrast, if males can only decrease predation risk through reduction of reproductive effort (e.g. decrease colouration or calling rates), then increasing predation risk causes immune function to increase. If males can utilize multiple defense strategies and sexual selection is low, then males maintain a constant immune function as predation risk increases. Sexual selection robustly resulted in decreased immunocompetence. Overall, our results suggest that predation plays an important role in the evolution of sexual dimorphism in immunocompetence, but predicting its effect requires understanding the integrated defense strategies available.