Experimental support for the cost–benefit model of lizard thermoregulation: the effects of predation risk and food supply

According to Huey and Slatkin’s [Q Rev Biol 51:363–384, 1976] cost–benefit model of behavioural thermoregulation, lizards should adjust their thermoregulatory strategy between active thermoregulation and thermoconformity (no thermoregulation) according to the costs (time and energy spent thermoregulating, exposure to predators), benefits (optimised physiological performance) and thermal quality of environment associated with a given situation. However, Gilchrist’s [Am Nat 146:252–270, 1995] model of thermal specialisation suggests that apparently costly mechanisms of behavioural thermoregulation can greatly increase fitness if the optimal body temperature is achieved. Field studies of ectotherm thermoregulatory strategies under extreme cold conditions and experiments testing the effects of cool environments on thermoregulatory behaviour are surprisingly scarce. We conducted laboratory experiments to test if common lizards Zootoca vivipara (an active thermoregulator in the field) are able to switch between active thermoregulation and thermoconformity in response to different thermal environments. We found that lizards in treatments with an opportunity to reach their preferred body temperature thermoregulated accurately, maintained their level of daily activity and improved their body condition considerably. In contrast, lizards in the treatment where the preferred body temperature could not be reached became thermoconformers, decreased their daily activity (except for gravid females) and did not increase their body condition. Our results show that lizards can indeed change their thermoregulatory strategy but stress that maintaining the preferred body temperature and, thus, optimising the physiological performance have high priority in lizard behaviour.

The fiddler crab, Uca beebei, lives in individually defended burrows, in mixed-sex colonies on intertidal mud flats. Avian predation is common, especially of crabs unable to escape into burrows. Mating pairs form in two ways. Females either mate on the surface at their burrow entrance ('surface mating') or leave their own burrow and sequentially enter and leave ('sample') courting males' burrows, before staying in one to mate underground ('burrow mating'). We tested whether perceived predation risk affects the relative frequency of these mating modes. We first observed mating under natural levels of predation during one biweekly, semi-lunar cycle. We then experimentally increased the perceived predation risk by attracting grackles (Quiscalus mexicanus) to each half of the study site in two successive biweekly cycles. In each experimental cycle, crabs were significantly less likely to mate on the side with more birds. Moreover, on the side with elevated predation risk, the number of females leaving burrows to sample was greatly reduced relative to the number of females that surface-mated. Males waved less and built fewer mud pillars, which attract females, when birds were present. We discuss several plausible proximate explanations for these results and the effect of changes in predation regime on sexual selection.

The fat reserves of small birds are built up daily as insurance against starvation. They are believed to reflect a trade-off between the risks of starvation and predation such that in situations of high predation risk birds are expected either to reduce their fat reserves in response to mass-dependent predation risk or to increase them in response to foraging interruptions. We assessed the effect on fat reserves of experimentally altering the perceived (but not the actual) risk of predation of wild great tits at a winter feeding site. The perceived predation risk was alternated between 'safe' and 'risky'. Increasing the perceived risk of predation involved 'swooping' a model sparrowhawk over the feeder at four unpredictable times each day using a remote mechanism We produce evidence that the experiment was suceessfull in altering the perceived risk of predation. As predicted from the hypothesis of mass-dependent predation risk, great tits (Parus major) carried significantly reduced fat reserves during the 'risky' treatment. Furthermore, dominant individuals were able to reduce their reserves more than subordinates. As birds returned to feeders within seconds after a predator 'attack', the reduction in fat reserves cannot be attributed to an interruption in feeding.

Influence du risque du a la presence de predateurs et a au jeune subit sur le taux d'accouplement et sur sa duree

To understand the effects of environmental changes on ecosystems, it is important to determine the factors and mechanisms influencing the strength of species interactions in food webs. However, joint effects of predation risk and additional environmental factors on species interaction strengths in multitrophic systems remain largely unexplored, leaving a substantial gap in our understanding of the links between local environmental characteristics and food web properties. To fill this gap, we investigated the effects of habitat complexity and predation risk by top predatory dragonfly larvae (Aeshna cyanea) on feeding rates and energetic efficiency (i.e. the ratio of acquired and expended energy) of the larvae of three intermediate predatory odonate species (Libellula quadrimaculata, Sympetrum sanguineum, and Ischnura elegans) preying on cladocerans. We hypothesised that predation risk would decrease the feeding rate, especially in the structurally simple habitat, and increase the metabolic rate of all intermediate predators. We also expected higher feeding rates of intermediate predators using aquatic vegetation as a perching site (i.e. Sympetrum and Ischnura) in the structurally complex habitat. Finally, we expected to observe habitat‐ and predation risk‐dependent energetic efficiencies of the intermediate predators driven by changes in feeding and metabolic rates. The effect of predation risk on feeding rates was species specific and differed between the structurally simple and complex habitat. Habitat complexity increased feeding rates but only in the absence of predation risk. Moreover, predation risk signalled by chemical cues significantly increased Sympetrum vulgatum feeding rates but did not influence the feeding rates of the two other intermediate predators. Metabolic rates varied among the three intermediate predators but were not affected by predation risk. Estimated energetic efficiency decreased with intermediate predator body mass and depended, to a lesser extent, on the interactive effect of habitat complexity and predation risk. Our results imply that the effects of habitat complexity and predation risk on trophic interactions are likely to be determined by traits related to foraging and defence of the intermediate predators and their habitat domains, and that energetic efficiency is mainly determined by predator mass. Given that habitat complexity and predation risk can vary substantially across habitats, we conclude that it is important to consider habitat complexity and predation risk to better understand and predict the effects of environmentally driven variations on trophic interaction strength and metabolic rates that underlie the energetic efficiency of individual consumers. This has important implications for population and community dynamics as well as ecosystem functioning.

Predation Risk Affects Mate Choice in a Gobiid Fish

Experimental studies incorporating multiple trophic levels are scarce but of increasing interest for understanding ecological communities. Here we investigated interactive effects of perceived predation risk and parasite pressure on life‐history traits in a hole‐nesting bird, and the effects of predation risk on parasite success. In a 3 × 2 experimental design we increased perceived predation risk for breeding great tits Parus major via simulations of either nest‐predators (woodpeckers) or post‐fledging predators (sparrowhawks) close to nests, and used a non‐predatory species (song thrush) as a control. Concurrently, half of the nests in each treatment were either infested with ectoparasites, or kept parasite‐free.Regarding the predation risk – parasite interaction, exposure to nest‐predators tended to lower wing and sternum growth rates of nestlings in the absence, but not the presence, of parasites. In the presence of parasites, exposure to a post‐fledging, but not to a nest‐predator, led to significantly reduced wing growth. Mass and tarsus length were not affected by predator exposure, but ectoparasites had slight positive effects on mass gain. In the last third of the nestling period, overall nestling size was significantly smaller when exposed to a post‐fledging predator than to a nest‐predator, but neither differed from the control. Parental feeding rates were not affected by the treatments, but parents became less selective towards food items under either predation risk. Hen‐flea population sizes (adult or larvae) in nests were not affected by predation risk treatment of hosts.In summary, we found some evidence for an interactive effect of predation risk and parasite pressure on nestling growth. The complexity of the interaction, combined with certain inconsistencies of the effects and potential statistical artifacts, prevent however a straightforward interpretation of the results. The insights from the study are useful for designing additional experiments to further investigate the complexity of predator–parasite interactions in wild populations.

The presence of a predator can result in the alteration, loss or reversal of a mating preference. Under predation risk, females often change their initial preference for conspicuous males, favouring less flashy males to reduce the risk of being detected by predators. Previous studies on predator‐induced plasticity in mate preferences have given females a choice between more and less conspicuous conspecific males. However, in species that naturally hybridize, it is also possible that females might choose an inconspicuous heterospecific male over a conspicuous conspecific male under predation risk. Our study addresses this question using the green swordtail (Xiphophorus helleri) and the southern platyfish (Xiphophorus maculatus), which are sympatric in the wild. We hypothesized that X. helleri females would prefer the sworded conspecific males in the absence of a predator but favour the less conspicuous, swordless, heterospecific males in the presence of a predator. Contrary to our expectation, females associated more with the heterospecific male than the conspecific male in the control (no predator) treatment, and they were non‐choosy in the predator treatment. This might reflect that females were attracted to the novel male phenotype when there was no risk of predation but became more neophobic after predator exposure. Regardless of the underlying mechanism, our results suggest that predation pressure may affect female preferences for conspecific versus heterospecific males. We also found striking within‐population, between‐individual variation in behavioural plasticity: females differed in the strength and direction of their preferences, as well as in the extent to which they altered their preferences in response to changes in perceived predation risk. Such variation in female preferences for heterospecific males could potentially lead to temporal and spatial variation in hybridization rates in the wild.

Predation risk is an environmental stressor that can induce changes in prey behavior and physiology. Perception of predation risk may indirectly affect offspring traits and future fitness prospects via impacts on the condition of parents. Females may influence the survival of their offspring via maternal effects, especially when breeding in stressful conditions. We investigated the effects of continuous predation risk perceived by mothers on the maternal allocation of immune factors and carotenoids in eggs of the pied flycatcher Ficedula hypoleuca . We collected eggs from wild pied flycatchers that bred in the vicinity of a predator nest (pygmy owl Glaucidium passerinum ), were exposed to cues of a mammalian nest predator (urine of least weasel Mustela nivalis ), or received appropriate controls for these two groups. Pied flycatchers transferred more immunoglobulin in eggs under high predation risk in both owl and mammalian predator treatments. The presence of owl nests also lowered the level of lysozyme transferred in the eggs in one of the two study years. Predation risk did not modify egg size or overall carotenoid levels. Our results show that continuous predation risk perceived by females during egg‐laying affects egg composition. This different allocation of maternal immune factors may be an adaptive response evolved to increase the probability of offspring survival.

The important ecological role of predation risk in shaping populations, communities and ecosystems is becoming increasingly clear. In this context, synergistic effects between predation risk and other natural stressors on prey organisms are gaining attention. Although non-pathogenic bacteria can be widespread in aquatic ecosystems, their role in mediating effects of predation risk has been ignored. We here address the hypothesis that non-pathogenic bacteria may reinforce the negative effects of predation risk in larvae of the damselfly Coenagrion puella. We found synergistic effects for all three life history variables studied: mortality increased, growth reductions were magnified and bacterial load was higher when both non-lethal stressors were combined. The combined exposure to the bacterium and predation risk considerably impaired the two key antipredator mechanisms of the damselfly larvae: they no longer reduced their food intake under predation risk and showed a synergistic reduction in escape swimming speed. The reinforcing negative effects on the fitness-related traits could be explained by the observed synergistic effects on food intake, swimming muscle mass, immune function and oxidative damage. These are likely widespread consequences of energetic constraints and increased metabolic rates associated with the fight-or-flight response. We therefore hypothesize that the here documented synergistic interactions with non-pathogenic bacteria may be widespread. Our results highlight the ignored ecological role of non-pathogenic bacteria in reinforcing the negative effects of predation risk on prey organisms.

Combined effects of insecticide exposure and predation risk on freshwater detritivores.

The effects of predation risk on the use of social foraging tactics

Perceived predation risk predicts glucocorticoid hormones, but not reproductive success in a colonial rodent

Parents routinely encounter stress in the ecological environment that can affect offspring development (transgenerational plasticity: TGP); however, parents' interactions with conspecifics may alter how parents respond to ecological stressors. During social buffering, the presence of conspecifics can reduce the response to or increase the speed of recovery from a stressor. This may have cascading effects on offspring if conspecifics can mitigate parental responses to ecological stress in ways that blunt the transmission of stress-induced transgenerational effects. Here, we simultaneously manipulated both paternal social isolation and experience with predation risk prior to fertilisation in threespined stickleback (Gasterosteus aculeatus). We generated offspring via in-vitro fertilisation to allow us to isolate paternal effects mediated via sperm alone (i.e. in the absence of paternal care). If social buffering mitigates TGP induced by paternal exposure to predation risk, then we expect the transgenerational effects of predation exposure to be weaker when a conspecific is present compared to when the father is isolated. Offspring of predator-exposed fathers showed reduced anxiety-like behaviour and tended to be captured faster by the predator. Fathers who were socially isolated also had offspring that were captured faster by a live predator, suggesting that paternal social isolation may have maladaptive effects on how offspring respond to ecological stressors. Despite additive effects of paternal social isolation and paternal predation risk, we found no evidence of an interaction between these paternal treatments, suggesting that the presence of a conspecific did not buffer fathers and/or offspring from the effects of predation risk. Our results suggest that socially induced stress is an important, yet underappreciated, mediator of TGP and can elicit transgenerational effects even in species that do not form permanent social groups. Future studies should therefore consider how the parental social environment can affect both within and trans-generational responses to ecological stressors.

Imminent predation risk affects mating behaviours in prey individuals in a multitude of ways that can theoretically impact the strength of sexual selection, as well as its operation on traits. However, empirical studies of the effects of imminent predation risk on sexual selection dynamics are still scarce. Here we explore how perceived predation affects: (1) the relationship between the opportunity for selection and the actual strength of selection on male traits; and (2) which traits contribute to male fitness and the shape of selection on these traits. We simulate two consecutive reproductive episodes, under control conditions and perceived predation risk using experimental populations of Trinidad guppies. The opportunity for selection is higher under predation risk compared to the control condition, but realised selection on traits remains unaffected. Pre- and postcopulatory traits follow complex patterns of nonlinear selection in both conditions. Differences in selection gradients deviate from predictions based on evolutionary and non-lethal effects of predation, the most notable being strong disruptive selection on courtship rate under predation risk. Our results demonstrate that sexual selection is sensitive to imminent predation risk perception and reinforce the notion that both trait-based and variance-based metrics should be employed for an informative quantification.