Adaptive changes in prey vulnerability shape the response of predator populations to mortality

Simple models are used to explore how adaptive changes in prey vulnerability alter the population response of their predator to increased mortality. If the mortality is an imposed harvest, the change in prey vulnerability also influences the relationship between harvest effort and yield of the predator. The models assume that different prey phenotypes share a single resource, but have different vulnerabilities to the predator. Decreased vulnerability is assumed to decrease resource consumption rate. Adaptive change may occur by phenotypic changes in the traits of a single species or by shifts in the abundances of a pair of coexisting species or morphs. The response of the predator population is influenced by the shape of the predator's functional response, the shape of resource density dependence, and the shape of the tradeoff between vulnerability and food intake in the prey. Given a linear predator functional response, adaptive prey defense tends to produce a decelerating decline in predator population size with increased mortality. Prey defense may also greatly increase the range of mortality rates that allow predator persistence. If the predator has a type-2 response with a significant handling time, adaptive prey defense may have a greater variety of effects on the predator's response to mortality, sometimes producing alternative attractors, population cycles, or increased mean predator density. Situations in which there is disruptive selection on prey defense often imply a bimodal change in yield as a function of harvesting effort, with a minimum at intermediate effort. These results argue against using single-species models of density dependent growth to manage predatory species, and illustrate the importance of incorporating anti-predator behavior into models in applied population ecology.     

Uniform persistence for sigmoidal diet selection with keystone prey species

In this paper we discuss uniform persistence (UP) criteria of two prey- one predator systems, where we consider that the predator's diet selection is a sigmoidal function of the most profitable prey type in place of a step function of conventional diet choice theory. We also derive UP results of the system with direct interspecific competition between the prey. The role of the most profitable prey item as a keystone species, the magnitude of its carrying capacity, the ability to withstand predation of both prey species, and the ratios of their profitability values (to predators) are important to whether or not adaptive foraging may promote UP. In general, foraging decision rules play no role in UP if the alternative prey item is the keystone species. The result is also not affected by the effect of direct competitive coexistence or dominance relationship of the prey. In some cases, dominance of one of the prey species provides the most advantageous situation for ensuring UP. Received: 1 February 1999 / Revised version: 20 September 1999 / Published online: 4 July 2000     

Cheating on a mutualism: indirect benefits of ant attendance to a coccidophagous coccinellid

Coccinellids (Coleoptera: Coccinellidae) are generally unable to prey on ant-tended prey. However, particular coccinellid species have morphological, behavioral, or chemical characteristics that render them immune to ant attacks, and some species are even restricted to ant-tending areas. The benefit gained from living in close association with ants can be twofold: (1) gaining access to high-density prey areas and (2) gaining enemy-free space. Here, the myrmecophily of Azya orbigera Mulsant (Coleoptera: Coccinellidae), an important predator of the green coffee scale, Coccus viridis (Green) (Hemiptera: Coccidae), is reported. In this paper, three main questions were studied. (1) Are the waxy filaments of A. orbigera larvae effective as defense against attacks of the mutualistic ant partner of C. viridis, Azteca instabilis F. Smith (Hymenoptera: Formicidae)? (2) Does A. instabilis reduce the rate at which A. orbigera larvae prey on scales? (3) Do A. orbigera larvae gain enemy-free space by living in close association with A. instabilis? Laboratory and field experiments were conducted to answer these questions. We found that, because of the sticky waxy filaments of A. orbigera larvae, A. instabilis is incapable of effectively attacking them and, therefore, the predation rate of A. orbigera on C. viridis does not decrease in the presence of ants. Furthermore, A. instabilis showed aggressive behavior toward A. orbigera's parasitoids, and the presence of ants reduced the parasitism suffered by A. orbigera. This is the first time that this kind of indirect positive effect is reported for an ant and a coccidophagous coccinellid. Furthermore, this indirect positive effect may be key to the persistence of A. orbigera's populations.     

Effect of plants on the searching efficiency of a generalist predator: the importance of predator-prey spatial association

In most studies of tritrophic interactions, the effect of plants on predators is confounded with changes in prey and predator behaviors after an encounter event. Here, we estimate how the effect of plants on prey distribution (in the absence of the predator) and on predator foraging behavior (in the absence of prey) may influence predation rate of Orius insidiosus (Say) (Heteroptera: Anthocoridae) in 11 plant by prey species combinations. The within-leaf distributions of O. insidiosus and its prey overlapped most on bean plants. The predator's foraging behavior (e.g., walking speed, turning rate) also differed among plant species. Simulations, using the prey distribution data and predator's foraging patterns on leaf surfaces of each plant species, show that, overall, the searching efficiency of O. insidiosus was higher on leaves of bean and corn than of tomato. However, the predator's searching efficiency was not consistent within plant species. Thus, the combined effect of plants directly on the predator and indirectly through the prey influenced the predator's searching efficiency.     

Dynamics of prey-flock escaping behavior in response to predator's attack

The dynamic behavior of prey-flock in response to predator's attack was investigated by using molecular dynamics (MD) simulations in a two-dimensional (2D) continuum model. By locally applying interactive forces between prey individuals (e.g. attraction, repulsion, and alignment), a coherently moving state in the same direction was obtained among individuals in prey-flock. When a single predator was introduced to the prey population, the prey-flock was correspondingly deformed by the predator's continuous attacks towards the prey-flock's center. In response to the predator's attack, three regimes in the flock size (compression (Regime I), expansion (Regime II), compression (Regime III)) were revealed if the predator's attack speed (kappa) was comparatively low to the escape speed of prey-flock. If noise was added to the predator's attacking course, a higher degree of variation was observed in the patterns of compression and expansion in the prey-flock size. However, the scaling behavior in the changes in prey-flock size was present in different levels of noise with the increase in predation risk (R) when kappa takes an appropriately low value. During the procedure of escaping, order breaking in alignment (phi) of prey population was observed, while the degree of alignment was dependent upon the changes in parameters of kappa and R.     

Predator functional response changed by induced defenses in prey

Functional responses play a central role in the nature and stability of predator-prey population dynamics. Here we investigate how induced defenses affect predator functional responses. In experimental communities, prey (Paramecium) expressed two previously undocumented inducible defenses--a speed reduction and a width increase--in response to nonlethal exposure to predatory Stenostomum. Nonlethal exposure also changed the shape of the predator's functional response from Type II to Type III, consistent with changes in the density dependence of attack rates. Handling times were also affected by prey defenses, increasing at least sixfold. These changes show that induced changes in prey have a real defensive function. At low prey densities, induction led to lower attack success; at high prey densities, attack rates were actually higher for induced prey. However, induction increased handling times sufficiently that consumption rates of defended prey were lower than those of undefended prey. Modification of attack rate and handling time has important potential consequences for population dynamics; Type III functional responses can increase the stability of population dynamics and persistence because predation on small populations is low, allowing a relict population to survive. Simulations of a predator-prey population dynamic model revealed the stabilizing potential of the Type III response.     

Individual base model of predator-prey system shows predator dominant dynamics

Individual base model of predator-prey system is constructed. Both predator and prey species have age structure and cohorts of early reproductive age have competitive advantage. The model has linear functional response in predation behavior and includes the effect of interference among predators and delay of population growth from resource intake, not by functional response but by calculation procedure. Each foraging action is calculated successively and surplus or scarce of acquired resources is interpreted into population size through individual birth and death. This model shows that biomass of prey killed by predator is dependent on demand of predator and that heterogeneity in predator population is essential in persistency and stability of predator-prey system. Heterogeneity of predator makes predator individuals of less competing ability die rapidly. Rapid death of weak individuals causes rapid decrease of total demand of predator and that makes enough room for survived predators. Therefore, the biomass of killed prey is dependent on predator's demand. As young or infant population of predator are the more vulnerable to shortage of prey, and when many of them cannot survive to reproductive age, they can stabilize the system by wasting excessive prey with only temporal numerical increase of predator population.     

The evolution of rates of successful and unsuccessful predation

Summary The question, how will evolutionary change in a predator or in its prey change the ratio of the rate of successful captures to the rate of unsuccessful capture attempts is addressed. I argue that this ratio is not a good index of the predator's adaptation to prey capture, because decreased costs of capture attempts or increased assimilation efficiency (both favored by natural selection in the predator) will usually reduce the ratio. In addition, the evolution of increased ability to capture prey may lead to a reduction in the success/failure ratio. Analysis of several simple models suggests that this result is robust. The presence of unsuccessful predation does have an important influence on the evolution of predator traits that increase its rate of encounter with the prey; the presence of unsuccessful predation may cause the predator to increase its adaptations for prey detection in response to an increase in the prey's ability to avoid detection.     

Dancing between the devil and deep blue sea: the stabilizing effect of enemy-free and victimless sinks

Theoretical and empirical studies have shown that enemy–victim interactions in spatially homogenous environments can exhibit diverging oscillations which result in the extinction of one or both species. For enemy–victim models with overlapping generations, we investigate the dynamical implications of spatial heterogeneity created by enemy-free sinks or victimless sinks. An enemy-free sink is a behavioral, physiological or ecological state that reduces or eliminates the victim's vulnerability to the enemy but cannot sustain the victim population. For victims that move in an ideal-free manner, we prove that the inclusion of an enemy-free sink shifts the population dynamics from diverging oscillations to stable oscillations. During these stable oscillations, the victim disperses in an oscillatory manner between the enemy-free sink and the enemy-occupied patch. Enemy-free sinks with lower mortality rates exhibit oscillations with smaller amplitudes and longer periods. A victimless sink, on the other hand, is a behavioral, physiological or ecological state in which the enemy has limited (or no) access to its victims. For enemies that move in an ideal-free manner, we prove that victimless sinks also stabilize diverging oscillations. Simulations suggest that suboptimal behavior due to information gathering or learning limitations amplify oscillations for systems with enemy-free sinks and dampen oscillations for systems with victimless sinks. These results illustrate that the coupling of a sink created by unstable enemy–victim interactions and a sink created by unsuitable environmental conditions can result in population persistence at the landscape level.     

Shadows of predation: habitat-selecting consumers eclipse competition between coexisting prey

Ecologists have made substantial progress evaluating the influences of adaptive behaviors on population dynamics and communities. But no-one has examined the joint influences of stochastic variation, predators, and density-dependent habitat selection on our interpretations of species coexistence. I begin the search with simulation models of habitat isodars (lines along which the fitness of individuals is identical in two or more habitats) assuming ideal-free habitat selection by two prey species exploited by a habitat-selecting parasitoid predator. The models include both regulating and non-regulating stochasticity. The intriguing results include the following: (1) all three species often achieved a true ideal-free distribution; (2) predators reduced prey population sizes and increased the frequency of local habitat extinctions; (3) despite the predator's differential reduction of prey densities, there was no evidence of apparent competition; (4) all species exhibited pulses of dispersal associated with donor–receiver population dynamics; (5) isodars produced valid estimates of competition between prey only in constant environments lacking habitat-selecting predators; (6) habitat-selection by predators forced prey into their preferred habitats; (7) the resulting ghost of competition obscured the prey species' competitive interaction; (8) isodars correctly revealed density-dependent habitat selection by the predator. Overall, the results appeared to depend primarily on the predator's habitat choice, rather than on prey trade-offs between competitive ability and reduced value (handling time) to the predator. Habitat selection theory, and its revelation via isodars, can thus provide considerable insight into processes affecting real communities, and most especially if ecologists assess carefully the constraints for their analysis and interpretation. Nevertheless, isodars designed to measure competition are likely to be most reliable in donor-controlled or experimental systems where regulating stochasticity has relatively little influence on prey dynamics.     

Subtle cues of predation risk: starlings respond to a predator's direction of eye-gaze

For prey animals to negotiate successfully the fundamental trade-off between predation and starvation, a realistic assessment of predation risk is vital. Prey responses to conspicuous indicators of risk (such as looming predators or fleeing conspecifics) are well documented, but there should also be strong selection for the detection of more subtle cues. A predator's head orientation and eye-gaze direction are good candidates for subtle but useful indicators of risk, since many predators orient their head and eyes towards their prey as they attack. We describe the first explicit demonstration of a bird responding to a live predator's eye-gaze direction. We present wild-caught European starlings (Sturnus vulgaris) with human 'predators' whose frontal appearance and gaze direction are manipulated independently, and show that starlings are sensitive to the predator's orientation, the presence of eyes and the direction of eye-gaze. Starlings respond in a functionally significant manner: when the predator's gaze was averted, starlings resumed feeding earlier, at a higher rate and consumed more food overall. By correctly assessing lower risk and returning to feeding activity earlier (as in this study), the animal gains a competitive advantage over conspecifics that do not respond to the subtle predator cue in this way.     

Effect of prey size on attack components of the functional response by Notonecta undulata

The number of encounters per prey, the proportion of encounters resulting in attacks, and the proportion of attacks that were successful were observed while fourth-instar Notonecta undulata nymphs preyed on smaller N. undulata nymphs. While encounters per prey and proportion of encounters resulting in attacks increased with prey size, the proportion of attacks that were successful decreased. The increase in encounter rate per prey was due in part to an increase in the predator's reactive distance to prey as prey size increased. While none of the attack parameters varied significantly with prey density, logarithmic regression of the number of encounters per unit search time on prey density suggested that prey density tends to have a positive effect on encounters per first-instar prey but a negative effect on encounters per second-instar prey. A functional response model is presented that incorporates components of the predator's attack rate as exponential functions of prey density and allows for effects of the time the predator may spend evaluating prey encountered but not attacked and time spent attacking prey not captured. Estimates of the attack parameters derived from the experimental data are used in the model to generate functional response curves for fourth-instar N. undulata preying on first- or second-instar conspecifics. The predicted curve for second-instar prey is typical type II but the curve for firstinstar prey is slightly positively density dependent at low prey densities, i.e., type III.     

Foraging behaviour in fishes: perspectives on variance

Synopsis The positive relationship between size of prey and frequency of ingestion by predators has been a focal point of investigations in foraging ecology. Field studies compare the frequency distribution of prey sizes in the predator's gut with that in the environment. Laboratory and field (enclosure) studies are based upon comparison of the frequency distributions of prey sizes in controlled environments, before and after the introduction of a predator. Optimal caloric return for foraging effort (i.e. the theory of optimal foraging) has been widely used as a guiding principle in attempts to explain what a fish consumes. There is a body of information, however, which seems to indicate that the perceptual potentialities and cognitive abilities of a predator can account for both the direction of the prey size versus ingestion frequency relationship and the variance surrounding it. Part of this variance may be evidence of systematic ambiguity, a property of cognitive skills causing predators to respond to the same stimulus in different ways and to different stimuli in the same way. More extensive examination of cognitive skills (minimally defined as learning, remembering and forgetting) in fish may permit causal interpretations (immediate and ultimate) of variance in predatory skills. In such a paradigm of foraging behaviour, environmental stimulus is not taken as the predator's object of response (percept); a cognitive representation connects mind to stimulus and this is the criterion for the act of perception. Cognition, here considered as a formal system which acts upon representations, connects mind to response and thus to adaptation. Studies of the relationships among rates of learning, long and short-term memory, rates of forgetting, prey behavior, size and population turnover rates, lateralization of brain functions, diel fluctuations in predator activity levels and sleep, experience, and critical periods in the development of the predator's nervous system should be examined in relation to foraging behaviour.     

The meaning of predatory specialization as illustrated by Aelurillus m-nigrum, an ant-eating jumping spider (Araneae: Salticidae) from Azerbaijan

The distinctions between a predator's diet, its prey-choice behaviour and its preference are illustrated in a study of Aelurillus m-nigrum Kulczyn'ski, a salticid spider from Azerbaijan. The natural diet of A. m-nigrum was determined from records of individuals feeding in the field (N=58). Ten arthropod orders were represented. Nine were from the class Insecta (Coleoptera, Collembola, Diptera, Heteroptera, Homoptera, Hymenoptera, Lepidoptera, Orthoptera, Psocoptera) and one from the class Arachnida (Araneae). Of 50 insects among the prey, 21 (42%) were Hymenoptera, with ants (family Formicidae) alone accounting for 31% of all prey records. Although the majority (69%) of the natural prey were not ants, results from prey-choice testing in the laboratory implied that A. m-nigrum preferred ants as prey. However, this preference was evident only when the testing environment included sand and a small stone. Our findings illustrate the importance of not conflating the concept of a predator's preference with the concept of a predator's natural diet and illustrate that physical features of a predator's habitat may be an important factor in influencing how strongly preference is expressed.     

Coevolutionary dynamics of adaptive radiation for food-web development

To investigate how complex food-webs can develop through repeated evolutionary diversification, a predator–prey model was analyzed. In the model, each individual has two traits: trait x as a predator and trait y as a prey. These traits constitute a two-dimensional phenotype space, in which the whole group of individuals are represented as a phenotype distribution. Predator–prey interactions among the phenotypes are determined by their relative positions in the phenotype space. Each phenotypic cluster was treated as a species. Each species evolves in y to escape from predation, while it evolves in x to chase their prey. Analytical investigation provided two predictions. First, coupled evolutionary diversifications of y and x may occur when the x of predators have caught up with their prey’s y, which may be repeated. Second, complex food-webs may develop when species’ competitive strengths are kept similar within the communities. If the functional response is close to the ratio-dependent response, the competitive strengths of all species are similar when the relationship between predators and prey corresponds to the ideal free distribution (IFD). These predictions were confirmed by numerical simulations. Electronic supplementary material  The online version of this article doi:() contains supplementary material, which is available to authorized users.     

The influence of light level on the functional response of a zooplanktonivorous fish

Summary Light and vision are clearly of significance in foraging behaviour by underyearling common bream [Abramis brama (L.)]. These fish are effective predators at 1.25 Lux but they were also shown to be capable of taking prey, at a reduced rate, at a much lower light intensity (less than 5x10^-3 Lux). In the latter case they may have been using sensory modes other than vision, perhaps involving tactile and/or olfactory stimuli.We investigated the influence of light level on the functional response of bream to Daphnia magna prey. At 1.25 Lux the predator showed a typical type II response. However, the relatively unfavourable conditions in the lower light intensity appear to have been responsible for generating a sigmoid type III functional response. Observations, using infra-red sensitive equipment, suggested a behavioural basis for this result. Thus, the predator's attack rate was not constant, but increased with prey density. The significance of the type III functional response is discussed, both in terms of predator energetics and predator-prey population stability.     

Predatory behavior of the praying mantis,Tenodera aridifolia II. Combined effect of prey size and predator size on the prey recognition

Predatory behavior of the praying mantis,Tenodera aridifolia, as a function of the combined effect of its size and the size of the prey was investigated by using prey models. Behavioral responses were almost identical through the nymphal development in the predator. As the mantis grew, it attacked larger prey models, suggesting that it recognizes the prey's size in accordance with its own body size. Regression analyses demonstrate that the ratio of the prey's volume to the cube and the square of the predator's length is a more important parameter for prey recognition than are the one-dimensional parameters of the prey's and the predator's sizes.     

Kleptoparasitic prey competition in shoaling fish: effects of familiarity and prey distribution

Familiarity is thought to stabilize dominance hierarchies andreduce aggressive interactions within groups of socially livinganimals. Though familiarity has been widely studied in shoalingfish, few studies have investigated changes in prey competitionas a function of time spent together within groups of initiallyunfamiliar individuals. In this study, we created shoals ofthree-spined stickleback (Gasterosteus aculeatus) and monitoredchanges in foraging rates and related competitive behaviorswithin shoals over a 4-week period in experimental series whereprey was spatially and temporally concentrated or dispersed.Prey share was unequal under both prey distribution modes, anddisparity in prey share was not seen to change as trials progressed.Interestingly, the contest rate for prey items fell over timewhen individuals were competing for dispersed prey but not whenprey were concentrated. We found no evidence that fish showedassociation preferences for either group members that had consumeda greater or lesser proportion of prey during trials. Thoughthe intensity of competition may be reduced by increased groupstability in nature, this is likely to be strongly dependenton the way prey resources are distributed through space andtime.     

Predator's invasion into an isolated patch with spatially heterogeneous prey distribution

The invasion success of a diffusing predator which changes its diffusion coefficient depending on whether the prey exists or not is investigated. The prey is assumed to be immobile and distributed in an isolated patch. The isolated patch consists of two kinds of region: prey-existing zone and prey-vacant zone. We discuss what relation a heterogeneity of prey distribution has with the predator's invasion success into the patch. Its spatial heterogeneity appears to affect significantly the predator's invasion. In an Appendix we briefly treat an analogous problem involving two competing species.     

The effect of predator and prey density on the induced defence of a ciliate

1. The level of antipredator defence should be proportional to the actual attack probability to minimize the cost of defence and maximize the net benefit.
2. The hypothesis that the induced antipredator morphology of Euplotes octocarinatus is a graded response to the actual risk of predation by Stylonychia mytilus was tested by manipulating the density of both prey and predator populations.
3. The magnitude of the response was graded according to both predator and prey density. A dense prey population may be protective since a prey is more exposed to a predator's attack as a solitary individual.
4. The results suggest that Euplotes is able to 'estimate' the real risk of predation and respond appropriately, without mobilizing more resources than needed.
5. Separation of the prey and predator with a nylon net revealed that the response was not induced by a water-transmitted factor but that direct cell-to-cell contacts were important. This finding departs from those of other studies.