Snake-like bird hisses induce anti-predator responses in a frog.

Some snakes emit hissing calls which are imitated by birds to deter potential predators. However, the effect of these snake and bird hisses on anuran risk recognition is not yet explored. Here we hypothesize that these hisses may advertise dangers to frogs and evoke their anti-predator responses. We used little torrent frogs (Amolops torrentis) as subjects and conducted sound playbacks to test their anti-predator behaviors. We found that little torrent frogs changed their calling behaviors during sympatric snake hiss playbacks, but showed no response to white noise and allopatric snake hiss playbacks. They did not respond to sympatric avian hiss that has low acoustic similarity with snake sounds. However, they decreased calling activity in response to sympatric avian hiss that has high acoustic similarity with snakes. As compared to other treatments, more individuals ceased calling during the playbacks of the highly similar bird hiss. These results suggest that frogs may recognize risks from snake and snake-like hissing calls and perform anti-predator responses.

On the importance of concomitant conditions: Light and conspecific presence modulate prey response to predation cue.

Assessment of individual costs of the anti-predator defence translating into changes in population parameters is meagre. This is because prey responses are likely to be modulated by additional factors, commonly present in the environment, but often neglected in experimental studies. To evaluate the effect of external factors on prey behavior and physiology, we exposed amphipods Dikerogammarus villosus and Gammarus jazdzewskii to the predation cue of Perca fluviatilis in different densities and light conditions. Singletons of both species exposed to the predation cue in light modified their oxygen consumption (D. villosus: reduction, G. jadzewskii: increase) compared to their respiration in predator-free conditions. However, in the presence of conspecifics or in darkness, their respiration became insensitive to the predation cue. On the other hand, the swimming activity of prey was reduced in the presence of the predation cue irrespective of prey density and light conditions, but singletons were consistently more active than groups. Thus, external factors, such as conspecifics and darkness, constantly or periodically occurring in the field, may reduce the costs of predator non-consumptive effects compared to the costs measured under laboratory conditions (in light or absence of conspecifics). Moreover, we showed that behavioral and physiological parameters of prey may change differently in response to predation risk. Thus, conclusions drawn on the basis of single defence mechanisms and/or results obtained in artificial conditions, not reflecting the environmental complexity, strongly depend on the experimental design and endpoint selection and therefore should be treated with care.

Effects of dispersant-treated oil upon behavioural and metabolic parameters of the anti-predator response in juvenile European sea bass (Dicentrarchus labrax).

Acute exposure to oil and oil dispersants can cause a wide range of physiological dysfunctions in marine fish species and evidences for consequences on behaviour are also increasing. In response to the presence of predators or to food availability, the modulation of locomotor activity and schools' behaviour enable fish to maximize their survival rates. However, the degree to which this regulatory process is affected by exposure to oil and/or dispersants is yet unknown. Here we investigated the effect of a 62-h experimental exposure to dispersant-treated oil on the behavioural (shoal cohesion, spontaneous activity) and metabolic (oxygen consumption) responses to simulated predation in juvenile European sea bass, Dicentrarchus labrax L. Our results suggest that exposure to petroleum hydrocarbons may affect negatively individual fitness through impaired ability to respond to predation. Shoal cohesion was not affected, but fish swimming activity was higher than control individuals under predation pressure and the amplitude of their metabolic response was significantly reduced. Fish recovered from alteration of their metabolic response 7 days post-exposure. Additionally, a strong habituation component was observed in C fish and the absence of such pattern in E fish suggest altered capacity to habituate over time to the surrounding environment and possible impairments of the related cognitive performances. Altogether, our data show that juvenile sea bass exposed to oil exhibit transient physiological dysfunctions and impairments of complex behaviours that may have major population-level consequences.

Larval habitat selection by females of two malaria vectors in response to predation risk.

For species lacking parental care, selection of a suitable habitat for their offspring, with a limited predation risk, is important. The ability of two African malaria mosquito females to detect a predation threat for their larvae was assessed through an oviposition choice test design. Our results suggest that gravid females of both Anopheles gambiae s.s. and An. coluzzii (Diptera, Culicidae) were able to detect the presence of a predator (Anisops jaczewskii, Notonectidae, Hemiptera; backswimmer). However, An. coluzzii were more likely to choose the cups containing predation cues while An. gambiae tended to avoid them for oviposition. Anopheles coluzzii females might use either alarm cues or pre-digestive cues from the external prey digestion to gauge the threat level, while An. gambiae females might use predator cues (odor or vibrations) or digestive cues from the predator. Compared to An. gambiae, An. coluzzii females seemed to accept the predation threat for their larvae to some extent. These results are consistent with the observed larval distribution in the field. Anopheles coluzzii larvae are found in complex permanent reservoirs in which the predation pressure is high, while An. gambiae larvae are more frequently found in temporary reservoirs with a lower predation threat. To our knowledge, this is the first time such a divergence in oviposition strategies regarding predation risk management by females is shown between closely related mosquito species.

Response of Bolivian gray titi monkeys (Plecturocebus donacophilus) to an anthropogenic noise gradient: behavioral and hormonal correlates.

Worldwide urban expansion and deforestation have caused a rapid decline of non-human primates in recent decades. Yet, little is known to what extent these animals can tolerate anthropogenic noise arising from roadway traffic and human presence in their habitat. We studied six family groups of titis residing at increasing distances from a busy highway, in a park promoting ecotourism near Santa Cruz de la Sierra, Bolivia. We mapped group movements, sampled the titis' behavior, collected fecal samples from each study group and conducted experiments in which we used a mannequin simulating a human intrusion in their home range. We hypothesized that groups of titi monkeys exposed to higher levels of anthropogenic noise and human presence would react weakly to the mannequin and show higher concentrations of fecal cortisol compared with groups in least perturbed areas. Sound pressure measurements and systematic monitoring of soundscape inside the titis' home ranges confirmed the presence of a noise gradient, best characterized by the root-mean-square (RMS) and median amplitude (M) acoustic indices; importantly, both anthropogenic noise and human presence co-varied. Study groups resided in small, overlapping home ranges and they spent most of their time resting and preferentially used the lower forest stratum for traveling and the higher levels for foraging. Focal sampling analysis revealed that the time spent moving by adult pairs was inversely correlated with noise, the behavioral change occurring within a gradient of minimum sound pressures ranging from 44 dB(A) to 52 dB(A). Validated enzyme-immunoassays of fecal samples however detected surprisingly low cortisol concentrations, unrelated to the changes observed in the RMS and M indices. Finally, titis' response to the mannequin varied according to our expectation, with alarm calling being greater in distant groups relative to highway. Our study thus indicates reduced alarm calling through habituation to human presence and suggests a titis' resilience to anthropogenic noise with little evidence of physiological stress.

Proportional fitness loss and the timing of defensive investment: a cohesive framework across animals and plants.

The risk of consumption is a pervasive aspect of ecology and recent work has focused on synthesis of consumer-resource interactions (e.g., enemy-victim ecology). Despite this, theories pertaining to the timing and magnitude of defenses in animals and plants have largely developed independently. However, both animals and plants share the common dilemma of uncertainty of attack, can gather information from the environment to predict future attacks and alter their defensive investment accordingly. Here, we present a novel, unifying framework based on the way an organism's ability to defend itself during an attack can shape their pre-attack investment in defense. This framework provides a useful perspective on the nature of information use and variation in defensive investment across the sequence of attack-related events, both within and among species. It predicts that organisms with greater proportional fitness loss if attacked will gather and respond to risk information earlier in the attack sequence, while those that have lower proportional fitness loss may wait until attack is underway. This framework offers a common platform to compare and discuss consumer effects and provides novel insights into the way risk information can propagate through populations, communities, and ecosystems.

Non-consumptive predator effects on prey population size: A dearth of evidence.

There is a large and growing interest in non-consumptive effects (NCEs) of predators. Diverse and extensive evidence shows that predation risk directly influences prey traits, such as behaviour, morphology and physiology, which in turn, may cause a reduction in prey fitness components (i.e. growth rate, survival and reproduction). An intuitive expectation is that NCEs that reduce prey fitness will extend to alter population growth rate and therefore population size. However, our intensive literature search yielded only 10 studies that examined how predator-induced changes in prey traits translate to changes in prey population size. Further, the scant evidence for risk-induced changes on prey population size have been generated from studies that were performed in very controlled systems (mesocosm and laboratory), which do not have the complexity and feedbacks of natural settings. Thus, although likely that predation risk alone can alter prey population size, there is little direct empirical evidence that demonstrates that it does. There are also clear reasons that risk effects on population size may be much smaller than the responses on phenotype and fitness components that are typically measured, magnifying the need to show, rather than infer, effects on population size. Herein we break down the process of how predation risk influences prey population size into a chain of events (predation risk affects prey traits, which affect prey fitness components and population growth rate, which affect prey population size), and highlight the complexity of each transition. We illustrate how the outcomes of these transitions are not straightforward, and how environmental context strongly dictates the direction and magnitude of effects. Indeed, the high variance in prey responses is reflected in the variance of results reported in the few studies that have empirically quantified risk effects on population size. It is therefore a major challenge to predict population effects given the complexity of how environmental context interacts with predation risk and prey responses. We highlight the critical need to appreciate risk effects at each level in the chain of events, and that changes at one level cannot be assumed to translate into changes in the next because of the interplay between risk, prey responses, and the environment. The gaps in knowledge we illuminate underscore the need for more evidence to substantiate the claim that predation risk effects extend to prey population size. The lacunae we identify should inspire future studies on the impact of predation risk on population-level responses in free-living animals.

Population dynamic consequences of fearful prey in a spatiotemporal predator-prey system.

Fear can influence the overall population size of an ecosystem and an important drive for change in nature. It evokes a vast array of responses spanning the physiology, morphology, ontogeny and the behavior of scared organisms. To explore the effect of fear and its dynamic consequences, we have formulated a predator-prey model with the cost of fear in prey reproduction term. Spatial movement of species in one and two dimensions have been considered for the better understanding of the model system dynamics. Stability analysis, Hopf-bifurcation, direction and stability of bifurcating periodic solutions have been studied. Conditions for Turing pattern formation have been established through diffusion-driven instability. The existence of both supercritical and subcritical Hopf-bifurcations have been investigated by numerical simulations. Various Turing patterns are presented and found that the change in the level of fear and diffusion coefficients alter these structures significantly. Holes and holes-stripes mixed type of ecologically realistic patterns are observed for small values of fear and relative increase in the level of fear may reduce the overall population size.

Modeling the Fear Effect in Predator-Prey Interactions with Adaptive Avoidance of Predators.

Recent field experiments on vertebrates showed that the mere presence of a predator would cause a dramatic change of prey demography. Fear of predators increases the survival probability of prey, but leads to a cost of prey reproduction. Based on the experimental findings, we propose a predator-prey model with the cost of fear and adaptive avoidance of predators. Mathematical analyses show that the fear effect can interplay with maturation delay between juvenile prey and adult prey in determining the long-term population dynamics. A positive equilibrium may lose stability with an intermediate value of delay and regain stability if the delay is large. Numerical simulations show that both strong adaptation of adult prey and the large cost of fear have destabilizing effect while large population of predators has a stabilizing effect on the predator-prey interactions. Numerical simulations also imply that adult prey demonstrates stronger anti-predator behaviors if the population of predators is larger and shows weaker anti-predator behaviors if the cost of fear is larger.

Does corticosterone mediate predator-induced responses of larval Hylarana indica?

Prey-predator interactions have been studied extensively in terms of morphological and behavioural responses of prey to predation risk using diverse model systems. However, the underlying physiological changes associated with morphological, behavioural or life historical responses have been rarely investigated. Herein, we studied the effect of chronic predation risk on larval growth and metamorphosis of Hylarana indica and the underlying physiological changes in prey tadpoles. In the first experiment, tadpoles were exposed to a caged predator from Gosner stage 25-42 to record growth and metamorphosis. Further, whole body corticosterone (CORT) was measured to determine the physiological changes underlying morphological and life historical responses of these prey tadpoles. Surprisingly, tadpoles experiencing continuous predation risk grew and developed faster and metamorphosed at a larger size. Interestingly, these tadpoles had significantly lower CORT levels. In the second experiment, tadpoles were exposed to predation risk (PR) or PR+CORT from stage 25-42 to determine the role of CORT in mediating predator-induced responses of H. indica. Tadpoles facing continuous predation risk grew and developed faster and metamorphosed at a larger size reinforcing the results of the first experiment. However, when CORT was administered along with predation risk, tadpoles grew and developed slowly leading to delayed metamorphosis. Interestingly, growth and metamorphic traits of tadpoles exposed to PR+CORT were comparable to those of the control group indicating that exogenous CORT nullified the positive effect of predation risk. Apparently, CORT mediates predator-induced morphological responses of H. indica tadpoles by regulating their physiology.