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Optimal Foraging and Predator-Prey Dynamics

A system consisting of a population of predators and two types of prey is considered. The dynamics of the system is described by differential equations with controls. The controls model how predators forage on each of the two types of prey. The choice of these controls is based on the standard assumption in the theory of optimal foraging which requires that each predator maximizes the net rate of energy intake during foraging. Since this choice depends on the densities of populations involved, this allows us to link the optimal behavior of an individual with the dynamics of the whole system. Simple qualitative analysis and some simulations show the qualitative behavior of such a system. The effect of the optimal diet choice on the stability of the system is discussed.

Journal Article↗

Effects of Optimal Antipredator Behavior of Prey on Predator-Prey Dynamics: The Role of Refuges.

The influence of optimal antipredator behavior of prey on predator-prey dynamics in a two-patch environment is studied. One patch represents an open habitat while the other is a refuge for prey. It is assumed that prey maximize their fitness measured by the instantaneous per capita growth rate. In each patch population dynamics is described by the Lotka-Volterra time continuous model. The refuge is characterized by its protectiveness which is inversely related to the predation risk for prey, and the dependence of population dynamics on protectiveness is studied. It is shown that adaptive behavior of prey changes qualitative properties of the underlying Lotka-Volterra model due to the appearance of a bounded attractor. Adaptive prey behavior does not lead to a stable equilibrium but to the reduction of population fluctuations. Dynamic consequences of a limited carrying capacity of the refuge are also considered. Low refuge carrying capacity leads to stability of predator-prey dynamics while stability is lost when the carrying capacity of the refuge is high. Lastly, it is shown that optimal antipredator behavior of prey leads to persistence and reduction of oscillations in population densities. Copyright 1998 Academic Press.

Journal Article↗

Identifying predator-prey processes from time-series.

The functional response is a key element in predator-prey models as well as in food chains and food webs. Classical models consider it as a function of prey abundance only. However, many mechanisms can lead to predator dependence, and there is increasing evidence for the importance of this dependence. Identification of the mathematical form of the functional response from real data is therefore a challenging task. In this paper we apply model-fitting to test if typical ecological predator-prey time series data, which contain both observation error and process error, can give some information about the form of the functional response. Working with artificial data (for which the functional response is known) we will show that with moderate noise levels, identification of the model that generated the data is possible. However, the noise levels prevailing in real ecological time-series can give rise to wrong identifications. We will also discuss the quality of parameter estimation by fitting differential equations to such time-series.

Algorithms↗

The value of fat reserves and the tradeoff between starvation and predation.

It is shown that in a range of models, the probability that a forager dies from starvation is, to a good approximation, an exponential function of energy reserves. Using a time and energy budget for a 19g passerine, we explore the consequences, in terms of starvation and predation, of various levels of energy reserves. It is shown that there exists an optimal level L* of reserves at which total mortality (starvation plus predation) is minimized. L* increases when the environment deteriorates as a result of a decrease in either temperature or mean gross gain or an increase in the mean search time. The effect of combined deteriorations is greater than the sum of their individual effects. At L*, the probability of predation is much higher than the probability of starvation. A simple analytic model suggests that this result will be fairly general, but also indicates conditions under which the result might not hold.

Adipose Tissue↗

On Liénard's equation and the uniqueness of limit cycles in predator-prey systems.

We study a system of ODE's modelling the interaction of one predator and one prey dx/dt = xg(x) - yp(x), dy/dt = gamma y[- delta - nu y - alpha y2 + h(x)]. This system defines a two-species community which incorporates competition among prey in the absence of any predators as well as a density-dependent predator specific death rate. This system is investigated under ecologically natural regularity conditions and assumptions on g, p and h to ensure the existence and uniqueness of limit cycles. The proof uses the standard Hopf-Andronov bifurcation theory and the technique of Liénard's equation.

Animals↗

Predator prey interactions with time delays.

A general (Volterra-Lotka type) integrodifferential system which describes a predator-prey interaction subject to delay effects is considered. A rather complete picture is drawn of certain qualitative aspects of the solutions as they are functions of the parameters in the system. Namely, it is argued that such systems have, roughly speaking, the following features. If the carrying capacity of the prey is smaller than a critical value then the predator goes extinct while the prey tends to this carrying capacity; and if the carrying capacity is greater than, but close to this critical value then there is a (globally) asymptotically stable positive equilibrium. However, unlike the classical, non-delay Volterra-Lotka model, if the carrying capacity of the prey is too large then this equilibrium becomes unstable. In this event there are critical values of the birth and death rates of the prey and predator respectively (which hitherto have been fixed) at which "stable" periodic solutions bifurcate from the equilibrium and hence at which the system is stabilized. These features are illustrated by means of a numerically solved example.

Animals↗

Predation of free-living engorged female Rhipicephalus appendiculatus.

In experiments done over a period of 1 1/2 years using engorged female Rhipicephalus appendiculatus tethered in a grass plot, 42% predation was observed in long grass (40-60 cm), and 36% in short grass (6-10 cm). Deaths due to environmental factors were 4.8% and 6.8% in long and short grass, respectively. Six groups of animals were confirmed to be predators of the ticks, namely: ants, spiders, rodents, birds, lizards and shrews. The implications of these results in making tick population models, and the possibility of using predators in integrated tick-control packages are discussed.

Animals↗

A predator prey model with age structure.

A general predator-prey model is considered in which the predator population is assumed to have an age structure which significantly affects it fecundity. The model equations are derived from the general McKendrick equations for age structured populations. The existence, stability and de-stabilization of equilibria are studied as they depend on the prey's natural carrying capacity and the maturation period m of the predator. The main result of the paper is that for a broad class of maturation functions positive equilibria are either unstable for small m or are destabilized as m decreases to zero. This is in contrast to the usual rule of thumb that increasing (not decreasing) delays in growth rate responses cause instabilities.

Aging↗

Interspecific interaction and predator avoidance behavior in response to tayra (Eira barbara) by mantled howler monkeys (Alouatta palliata).

This paper reports the response of one howler monkey group (Alouatta palliata) to a group of potential predators, the tayra (Eira barbara). The apparently successful predator avoidance behavior of the monkeys was recorded in detail. We observed a group of four adult tayras moving around the Alouatta group displaying a species-typical aggressive behavioral pattern. The two adult females of the howler group successfully chased the tayras away by repeatedly moving closer to the mustelids and even following them until the predators moved off.

Aggression↗

Loss of Estuarine Bacteria by Viral Infection and Predation in Microcosm Conditions.

The bacterioplankton density in Ria de Aveiro, a shallow estuarine ecosystem, varied in the broad range of 1.9-10.6 x 109 cells L-1. The range of values was about 2 times higher in brackish water than in marine water. At high tide bacterial abundance was 2-3 times lower than at low tide. The overall variation in virioplankton was in the range of 2.4-25.0 x 1010 particles L-1. Brackish water was about 2 times richer in viral particles than the marine water. Near low tide the virioplankton was 2-3 times higher that at high tide. Viral density followed the pattern of bacterial abundance (it explained 40% of virioplankton variation). The viruses to bacterium ratio varied, throughout tidal cycles, by a factor of about 10 establishing the range 4.7-55.6 (average 17.6). This ratio was rather similar in the two estuarine zones. We compared the effects of infection and predation on the control of bacterioplankton size in the two zones of the estuary. The approach to this question was conducted in experimental microcosms, set up in six combinations of plankton variables affecting the presence/absence of predators, virus-to-bacterium ratio (10-fold increase), virus-to-bacterium distance (2.2-fold increase), and bacterial growth rate. The results showed that predation was similar, in a percent basis, in marine (69%) and brackish water (73%). Viral infection was, however, higher in brackish water (59%) than in the marine water (36%). We conclude that the bacterioplankton along the salinity gradient evolves under biological pressures that are in different balance in the marine and brackish water zones. The effect of viral lysis on bacterial communities with enhanced growth (after yeast extract addition) was masked even when the initial ratio was 10-fold greater than in the natural samples. The high density of the virioplankton did not preclude the large and rapid increase in bacterial density. We suggest that the dynamics of the equilibrium between bacteria and viruses in the environment is driven to higher numerical levels during periods of intensive bacterial growth. On the contrary, at low bacterial growth rates the temporarily increased virus-to-bacterium ratio may drive the equilibrium to its lowest levels.

Journal Article↗

Changes in Synechococcus population size and cellular ribosomal RNA content in response to predation and nutrient limitation.

A mathematical model of predator-prey interactions was used to predict the relationship between population size and cellular growth rate in a two-tiered trophic system consisting of Synechococcus PCC 6301 and Tetrahymena pyriformis. As predicted, axenic chemostat cultures of Synechococcus responded to increased nutrient availability by expanding the equilibrium population size without a concurrent change in growth rate. Likewise, the addition of the predator Tetrahymena pyriformis decreased the Synechococcus population size by 85% and increased the Synechococcus growth rate. Synechococcus populations in the surface waters of the Gulf of Mexico were sampled to ascertain whether the relationship between population size and cellular 16S rRNA concentration conformed to that predicted by the model. Direct counts of autofluorescent cells in size-fractionated seawater samples provided an estimate of Synechococcus population size. The growth rate of in situ populations was estimated by measuring the extent of hybridization of an oligonucleotide probes complementary to Synechococcus 16S rRNA, based on evidence that ribosomal RNA content increases concurrently with growth rate. The comparison of in situ population sizes and specific growth rates revealed that relatively large Synechococcus populations were growing slowly, indicative of nutrient limitation, and that quickly growing populations were relatively small, as predicted for predator-limited populations.

Animals↗

Factors Affecting Predation by Cyclidium sp. and Euplotes sp. on PAH-Degrading and Nondegrading Bacteria.

Abstract If predators select for or against contaminant-degrading bacteria, it will affect bacterial survival and has important implications for bioremediation. Protozoa are important predators of bacteria. In order to determine whether protozoa preyed differentially on bacteria with different degradation abilities, two ciliates (Euplotes sp. and Cyclidium sp.) and three strains of PAH-degrading bacteria (Vibrio spp., degrading naphthalene, anthracene, or phenanthrene) were isolated from sediment from New York/New Jersey Harbor. By manipulating growth conditions, bacterial strains with different PAH-degradation abilities and different cell properties were produced. Stepwise regression models were used to analyze how clearance rates on suspended bacteria and grazing rates on bacteria attached to particles were affected by bacterial size, hydrophobicity, C:N ratio, protein content, and PAH-degradation ability. Clearance rates ranged from 0 to 49 nl ciliate-1 h-1 for Euplotes sp. and from 0 to 1.7 nl ciliate-1 h-1 for Cyclidium sp. Clearance rates of both ciliates were positively correlated with bacterial size, hydrophobicity, and protein content, and negatively correlated with C:N ratio. PAH degradation ability had no (for Euplotes sp.) or small (for Cyclidium sp.) effects on clearance rates. The models accounted for 63-75% of the variation in clearance rates on different bacteria. Only Euplotes sp. grazed on attached bacteria, at rates from 3 to 176 bacteria ciliate-1 h-1. A regression model with only C:N ratio and protein content explained 45% of the variation in grazing rates. These models indicate that multiple properties of bacteria affect their susceptibility to predation by ciliates, but PAH-degradation ability per se has little effect.

Journal Article↗

The rainbow bridge: Hamiltonian limits and resonance in predator-prey dynamics.

In the presence of seasonal forcing, the intricate topology of non-integrable Hamiltonian predator-prey models is shown to exercise profound effects on the dynamics and bifurcation structure of more realistic schemes which do not admit a Hamiltonian formulation. The demonstration of this fact is accomplished by writing the more general models as perturbations of a Hamiltonian limit, ℋ, in which are contained infinite numbers of periodic, quasiperiodic and chaotic motions. From ℋ, there emanates a surface, Gamma, of Nejmark-Sacker bifurcations whereby the annual oscillations induced by seasonality are destabilized. Connecting Gamma and ℋ is a bridge of resonance horns within which invariant motions of the Hamiltonian case persist. The boundaries of the resonance horns are curves of tangent (saddle-node) bifurcations corresponding to subharmonics of the yearly cycle. Associated with each horn is a rotation number which determines the dominant frequency, or "color", of attractors within the horn. When viewed through the necessarily coarse filter of ecological data acquisition, and regardless of their detailed topology, these attractors are often indistinguishable from multi-annual cycles. Because the tips of the horns line up monotonically along Gamma, it further follows that the distribution of observable periods in systems subject to fluctuating parameter values induced, for example, by year-to-year variations in the climate, will often exhibit a discernible central tendency. In short, the bifurcation structure is consistent with the observation of multi-annual cycles in Nature. Fundamentally, this is a consequence of the fact that the bridge between ℋ and Gamma is a rainbow bridge. While the present analysis is principally concerned with the two species case (one predator and one prey), Hamiltonian limits are also observed in other ecological contexts: 2n-species (n predators, n prey) systems and periodically-forced three level food chain models. Hamiltonian limits may thus be common in models involving the destruction of one species by another. Given the oft-commented upon structural instability of Hamiltonian systems and the corresponding lack of regard in which they are held as useful caricatures of ecological interactions, the pivotal role assigned here to Hamiltonian limits constitutes a qualitative break with the conventional wisdom.

Animals↗

Global analysis of the Michaelis-Menten-type ratio-dependent predator-prey system.

The recent broad interest on ratio-dependent based predator functional response calls for detailed qualitative study on ratio-dependent predator-prey differential systems. A first such attempt is documented in the recent work of Kuang and Beretta(1998), where Michaelis-Menten-type ratio-dependent model is studied systematically. Their paper, while contains many new and significant results, is far from complete in answering the many subtle mathematical questions on the global qualitative behavior of solutions of the model. Indeed, many of such important open questions are mentioned in the discussion section of their paper. Through a simple change of variable, we transform the Michaelis-Menten-type ratio-dependent model to a better studied Gause-type predator-prey system. As a result, we can obtain a complete classification of the asymptotic behavior of the solutions of the Michaelis-Menten-type ratio-dependent model. In some cases we can determine how the outcomes depend on the initial conditions. In particular, open questions on the global stability of all equilibria in various cases and the uniqueness of limit cycles are resolved. Biological implications of our results are also presented.

Animals↗

Predator-prey models with delay and prey harvesting.

It is known that predator-prey systems with constant rate harvesting exhibit very rich dynamics. On the other hand, incorporating time delays into predator-prey models could induce instability and bifurcation. In this paper we are interested in studying the combined effects of the harvesting rate and the time delay on the dynamics of the generalized Gause-type predator-prey models and the Wangersky-Cunningham model. It is shown that in these models the time delay can cause a stable equilibrium to become unstable and even a switching of stabilities, while the harvesting rate has a stabilizing effect on the equilibrium if it is under the critical harvesting level. In particular, one of these models loses stability when the delay varies and then regains its stability when the harvesting rate is increased. Computer simulations are carried to explain the mathematical conclusions.

Animals↗

Developmental responses to predation risk in morphologically defended mayflies.

Densities and species composition of predators could affect morphological defences, larval development and the timing of emergence of their prey. To address this issue we studied the morphology and life history of an ephemerellid mayfly, Ephemerella invaria, from two streams in a deciduous forested drainage basin in central New York. Both streams contained predatory fish, but densities and species composition of fish differed. A field survey provided evidence that Ephemerella inhabiting a stream with > or =10 fish species and high relative densities of fish emerged several weeks earlier and at smaller sizes than Ephemerella inhabiting a nearby tributary with approximately 2 fish species and low relative densities of fish. However, the two populations of mayflies showed no differences in defensive morphology or growth rates. In laboratory rearing experiments, we exposed Ephemerella larvae from these two locations to fish chemical cues or control water (no fish) over 2 months to test whether differences in life histories could be attributed to fish. Fish cues induced faster larval development, but also smaller size of mature Ephemerella individuals from both high and low predator locations. Although shorter development times in more dangerous environments could increase larval survival, smaller size of females results in a fecundity cost associated with this life history shift. Consistent with the field studies, laboratory rearing experiments revealed no effects of fish cues on Ephemerella's morphological defences. These data suggest that variation in the density or species composition of predators may favour the evolution of developmental plasticity to reduce mortality in the larval environment.

Adaptation, Physiological↗

Negative impacts of a vertebrate predator on insect pollinator visitation and seed output in Chuquiraga oppositifolia, a high Andean shrub.

Studies on plant-pollinator interactions have largely neglected the potential negative effects of the predators of pollinators on seed output, even though anti-predatory behaviour of pollinators may affect visitation patterns, pollen transfer, and therefore potentially, plant reproductive output. We tested the hypothesis that the presence of lizards and insectivorous birds, by reducing pollinator visitation, can have significant negative effects on seed output in the insect-pollinated, genetically self-incompatible lower alpine Andean shrub, Chuquiraga oppositifolia (Asteraceae). The lower alpine belt supports a high density of territorial Liolaemus (Tropiduridae) lizards and low shrubs interspersed among rocks of varying sizes, the latter inhabited by lizards and commonly used by flycatchers Muscisaxicola (Tyrannidae) as perching sites. In a 2x2 factorial predator-exclusion experiment, visitation rates of the most frequent pollinators of C. oppositifolia (the satyrid butterfly Cosmosatyrus chilensis and the syrphid fly Scaeva melanostoma), the duration of pollinator visits, and seed output, were 2-4 times greater when lizards were excluded, while birds had no effect. In a natural experiment, visits by S. melanostoma were 9 times shorter, and pollinator visitation rates of C. chilensis and S. melanostoma, and C. oppositifolia seed output were 2-3 times lower on shrubs growing adjacent to lizard-occupied rocks compared to those growing distant from rocks. Our results, verified for additional Andean sites, suggest that lizard predators can alter the behaviour of pollinators and elicit strong top-down indirect negative effects on seed output. Such effects may be especially important in high alpine plant communities, where pollinator activity can be low and erratic, and pollen limitation has been reported.

Altitude↗

Breeding suppression in free-ranging grey-sided voles under the influence of predator odour.

The breeding suppression hypothesis predicts that females of certain small mammal species will reduce reproduction as a response to the odour of a specialised mammalian predator. This was tested in a field experiment with grey-sided voles (Clethrionomys rufocanus) during three summer seasons (1997-1999) in the subalpine tundra of northern Norway, which is a natural habitat of this species. In a first phase free-ranging voles in six unfenced 1-ha plots were monitored by live-trapping from June to August each year. In a second phase from August to September, three of the plots were sprayed with weasel (Mustela nivalis) odour to simulate increased apparent predation risk, while the remaining three plots served as untreated controls. On all plots voles were individually marked with ear tattoos and were regularly live-trapped during the whole breeding season to follow their performance. On the treatment plots the recruitment rate of juveniles did not increase in late summer as it did on the control plots. The proportion of reproductively non-active adult females was significantly higher on the treatment plots for both old and young females. Our results thus verify the breeding suppression hypothesis for the first time under natural conditions. However, the response in overwintered females is in conflict with the original hypothesis because the assumed fitness benefits from breeding delayed until the next season are inaccessible to them. As an alternative explanation we propose a short-term response of reduced activity and interrupted breeding until the predator has exploited and left the feeding patch. Such a "duck and cover" strategy would increase the fitness of females of all age classes when prey habitats are patchy.

Adaptation, Physiological↗