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PubMed1977

Components of predation defense behavior in chickens: evidence for endogenous rhythmicity.

The manifestation of diurnal periodicity and the extent of its control by the photoperiod was assessed in three predation defense reactions which constitute either components or outcomes of a predator-prey interaction sequence. Two-hundred White Leghorn chicks were reared from hatching for one week in either 24L or 12L and then tested at one of two clock hours previously demonstrated to define peak and trough response for one of the components. Putative evidence was found for an endogenous source of the periodicity manifested in all reactions. Maintenance schedule did not entrain the periodicity, but simple room entry and handling elicited anti-predator reactions, the extent of which varied as a function of clock hour. A general model of predation defense behavior was proposed.

Animals↗
PubMed1986

Ventromedial tegmental lesions abolish offense without disturbing predation or defense.

Offense, defense, and predation, three kinds of aggressive behavior, are differentially affected by lesions of the ventromedial tegmentum of the brainstem of the rat. The lesions abolish offense while leaving defense and predation undisturbed. The offense behavior against another strange male, including bite-and-kick attack, offensive sideways posture, and offensive upright posture, was totally abolished, while the rats showed intact motor patterns of defensive upright posture, chasing, and killing bite in the tests for defense and predation. It is argued that these results support a motivational systems analysis of mammalian aggressive behavior. According to such an analysis, offense, defense, and predation are controlled by discrete motivational mechanisms located in different brainstem regions.

Aggression↗
PubMed1987

Predator-prey interactions between ectoparasites.

Vertebrates represent a resource frequently exploited by ectoparasites. But the ectoporosites themselves also represent a resource that can be exploited by specialized predators. Some o f these predators have been classified as ectoparasites, but in some cases the vertebrate blood in their crops comes from their blood-sucking prey. In fact, as Lance Durden explains, the assemblage o f arthropods that inhabit the vertebrate skin surface, or pelage, seems to show a complete spectrum of adaptations from predators to facultative and obligate blood-suckers, together with those feeding on other materials in this special habitat. The dynamics of their interactions are further complicated by responses of the host to the arthropods, and much further study is needed before the role o f predators in controlling ectoparasites can be clarified.

Journal Article↗
PubMed1984

Encounters in predator-prey systems: a simple discrete model.

Predator-prey systems are often described by exploitation models. These models can mimic experimental data very accurately, but it is sometimes difficult to realize the relationships between the models and the behavior of individual predator and prey animals. A simple discrete model is proposed here that tries to elucidate the connections between: the animals' movements, the predator/prey encounters; and the dynamics in the system as globally represented by the exploitation models. In these models, the term "area of discovery" plays an essential role. This term is shown to be a predictable coefficient that is composed of measurable physical properties of the analyzed predator-prey system. The model takes into account that predators and prey in experimental systems often do not search randomly but prefer some parts of the test area. The model is applied to the mite system Phytoseiulus persimilis/Tetranychus urticae under simple artificial conditions.

Animals↗
PubMed2005

Expression of egr-1 (zif268) mRNA in select fear-related brain regions following exposure to a predator.

Research has demonstrated that immediate-early genes/inducible transcriptional factors (e.g., c-fos, egr-1) are increased in amygdala nuclei (lateral, basal and central nuclei) known to be involved in fear conditioning, footshock stress and novelty. Although these data suggest that expression of inducible transcriptional factors are involved in fear, other non-shock ethologically based paradigms (predator or predator odor exposure) do not appear to increase c-fos in the lateral and basal nuclei. While the lack of c-fos expression may indicate that predator stress does not engage the lateral and basal amygdala nuclei, it may be that c-fos in the amygdala is not responsive to predator exposure. Therefore, egr-1, which increases in the lateral nucleus following fear conditioning, footshock and novelty, was assessed to determine if its expression is induced in rats exposed to a cat. Five minutes of cat exposure did not increase expression of egr-1 mRNA in the lateral nucleus of the amygdala. egr-1 was increased in the paraventricular nucleus of the hypothalamus, indicating cat-induced stress, and visual cortex compared to rats that were either confined for 5 min or handled. In the lateral periaqueductal gray, handled rats displayed a left hemisphere dominance, which disappeared in both the cat-exposed and confined group, suggesting that immobility, induced by either cat-induced stress or unstressed confinement, increased right hemisphere egr-1 expression. The results are discussed in a context of differences and similarities in neural circuitry for conditioned and unconditioned fear.

Animals↗
PubMed2004

Does mutual interference always stabilize predator-prey dynamics? A comparison of models.

Based on a qualitative analysis of ODE systems, the dynamic properties of alternative predator-prey models with predator-dependent functional response have been compared in order to study the role that predator interference plays in the stabilisation of trophic systems. The models considered for interference have different mathematical expressions and different conceptual foundations. Despite these differences, they give essentially the same qualitative results: when interference is low, increasing it has a positive effect on asymptotic stability and thus on the resilience of the biological system. When it is high, it is the contrary (with logistic prey growth, increasing the interference parameter ensures stability but leads to very small predator densities). Possible consequences on the evolution of the interference level in real ecosystems are discussed.

Animals↗
PubMed2006

Hair canopy of cricket sensory system tuned to predator signals.

Filiform hairs located on the cerci of crickets are among the most sensitive sensors in the animal world and enable crickets to sense the faintest air movements generated by approaching predators. While the neurophysiological and biomechanical aspects of this sensory system have been studied independently for several decades, their integration into a coherent framework was wanting. In order to evaluate the hair canopy tuning to predator signals, we built a model of cercal population coding of oscillating air flows by the hundreds of hairs on the cerci of the sand cricket Gryllus bimaculatus (Insecta: Orthoptera). A complete survey of all hairs covering the cerci was done on intact cerci using scanning electronic microscopy. An additive population coding of sinusoid signals of varying frequencies and velocities taking into account hair directionality delivered the cercal canopy tuning curve. We show that the range of frequencies and velocities at which the cricket sensory system is best tuned corresponds to the values of signals produced by approaching predators. The relative frequencies of short (< 0.5 x 10(-3) m) and long hairs and their differing responses to oscillating air flows therefore enable crickets to detect predators in a time-frequency-intensity space both as far as possible and at close range.

Action Potentials↗
PubMed2005

Reinforcement learning for a stochastic automaton modelling predation in stationary model-mimic environments.

In this paper we propose a mathematical learning model for the feeding behaviour of a specialist predator operating in a random environment occupied by two types of prey, palatable mimics and unpalatable models, and a generalist predator with additional alternative prey at its disposal. A well known linear reinforcement learning algorithm and its special cases are considered for updating the probabilities of the two actions, eat prey or ignore prey. Each action elicits a probabilistic response from the environment that can be favorable or unfavourable. To assess the performance of the predator a payoff function is constructed that captures the energetic benefit from consuming acceptable prey, the energetic cost from consuming unacceptable prey, and lost benefit from ignoring acceptable prey. Conditions for an improving predator payoff are also explicitly formulated.

Algorithms↗
PubMed2005

The smell of danger: a behavioral and neural analysis of predator odor-induced fear.

The odors of predators used in animal models provide, in addition to electric footshock, an important means to investigate the neurobiology of fear. Studies indicate that cat odor and trimethylthiazoline (TMT), a synthetic compound isolated from fox feces, are often presented to rodents to induce fear-related responses including freezing, avoidance, stress hormone and, in some tests, risk assessment behavior. Furthermore, we report that different amounts of cat odor impregnated on small-, medium-, or large-sized cloths impact the display of fear-related behavior when presented to rats. That is, rats exposed to a large cat odor containing cloth exhibit an increase in fear behavior, particularly freezing, which remains at high levels in habituation tests administered over a period of 7 days. The large cloth also induces a long-lasting increase in avoidance behavior during repeated habituation and extinction tests. A review of the brain regions involved in predator odor-induced fear behavior indicates a modulatory role of the medial amygdala, bed nucleus of the stria terminalis, and dorsal premammillary nucleus. In addition, the basolateral amygdala is involved in fear behavior induced by cat odor but not TMT, and the central amygdala does not appear to play a major behavioral role in predator odor-induced fear. Future research involving the use of predator odor is likely to rapidly expand knowledge on the neurobiology of fear, which has implications for understanding fear-related psychopathology.

Amygdala↗
PubMed2005

Recognition and avoidance of the odors of parasitized conspecifics and predators: differential genomic correlates.

In many species of animals chemical stimuli are an important source of information about the threats and dangers present in the social and non-social world. Olfactory cues play a fundamental role in modulating social recognition and interactions in a wide variety of mammals. Rodents, in particular, utilize chemical signals, to recognize and avoid conspecifics infected with parasites and other pathogens. Animals also respond to, and utilize, predator odor related information to assess and minimize their risk of predation. In this review, we briefly focus on the relations between odors, parasite recognition and avoidance and consider some of the associated hormonal, neural and genomic mechanisms. We describe how both male and female rodents distinguish between infected and uninfected males on the basis of odors, displaying aversive response to, and avoidance of, the urine odors of infected individuals. We further describe how the recognition and avoidance of the odors of infected individuals involves genes for the neuropeptide, oxytocin, (OT), and estrogenic mechanisms. We show that mice with deletions of the oxytocin gene (OT knockout mice (OTKO)) and mice whose genes for estrogen receptor (ER)-alpha or ER-beta [ER knockout mice (ERKO), alphaERKO and betaERKO] have been disrupted are specifically impaired in their recognition, avoidance, and memory of the odors of infected individuals. We contrast this with the recognition and display of aversive responses to predator (cat) odor that are insensitive to these genetic manipulations. These findings reveal some of the mechanisms associated with the olfactory mediated recognition of parasitized individuals and predators.

Animals↗
PubMed2005

Neural circuit changes mediating lasting brain and behavioral response to predator stress.

This paper reviews recent work which points to critical neural circuitry involved in lasting changes in anxiety like behavior following unprotected exposure of rats to cats (predator stress). Predator stress may increase anxiety like behavior in a variety of behavioral tests including: elevated plus maze, light dark box, acoustic startle, and social interaction. Studies of neural transmission in two limbic pathways, combined with path and covariance analysis relating physiology to behavior, suggest long term potentiation like changes in one or both of these pathways in the right hemisphere accounts for stress induced changes in all behaviors changed by predator stress except light dark box and social interaction. Findings will be discussed within the context of what is known about neural substrates activated by predator odor.

Action Potentials↗
PubMed2004

Thermal dependence of chemical assessment of predation risk affects the ability of wall lizards, Podarcis muralis, to avoid unsafe refuges.

Prey often respond to predators by increasing refuge use, but some refuges may expose prey to other types of predators. Because predators are not always visible inside refuges, their chemical stimuli may provide early warning of their presence. However, in ectotherms, chemosensory detection of predators may be thermally dependent. Lizards often hide in cold refuges, where their body temperature (Tb) may decrease, and this might affect their ability to detect chemicals of saurophagous snakes that ambush inside refuges. We examined the effects of Tb of wall lizards, Podarcis muralis, on their ability to detect chemicals of smooth snakes, Coronella austriaca. Differential tongue flick (TF) rates and behavioral patterns of lizards in response to scent of smooth snakes showed that lizards with optimal Tb discriminated and avoided the snake's scent, whereas lizards with suboptimal Tb did not. We also examined the importance of this effect on movement patterns and refuge use by lizards in terraria with safe (odorless) or unsafe refuges (snake-scented). While results of this experiment were variable, there was evidence of snake avoidance in that lizards at optimal Tb spent less time in snake-scented refuges relative to odorless refuges. Therefore, this study provides evidence that chemosensory discrimination of snake chemicals is thermally dependent, and, thus, suboptimal Tb impedes a lizard's ability to avoid snake-scented refuges.

Analysis of Variance↗
PubMed2004

Long-lasting, selective, anxiogenic effects of feline predator stress in mice.

Lasting increases in anxiety-like behavior (ALB) are produced by brief exposure of rats to a cat [Adamec RE, Shallow T, Lasting effects on rodent anxiety of a single exposure to a cat, Physiol. Behav., 54 (1993) 101-109.]. Mice also respond defensively to natural predator stimuli. Moreover, chronic exposure of mice to rat odor has immediate anxiogenic effects in plus maze and lasting (7 days) and effects on acoustic startle. The present study examined the lasting (7 days) after effects on ALB of a brief unprotected exposure of male CFW mice to a cat. Lasting effects on ALB of exposure to the cat exposure room were also assessed. Effects on behavior were studied in the hole board and elevated plus-maze (EPM). An ethological analysis of behavior revealed that risk assessment in the EPM was increased the most in predator-stressed mice. Mice exposed to the cat exposure room showed increased risk assessment falling between controls and cat exposed mice. Behavior in the hole board was unaffected, as were most other behaviors in the plus maze. Factor analysis revealed independence of risk assessment from other measures of ALB, activity and exploration, consistent with findings in rats. Aspects of the stress experience were highly predictive of later response to the cat. Cat biting and pawing, mouse fleeing and mouse weight measured at the time of cat exposure together accounted for 71% of the variance of risk assessment in cat exposed mice. The significance of these findings for vulnerability to cat predator stress of mice and for the use of predator stress in mice as a model of aspects of posttraumatic stress disorder (PTSD) are discussed.

Animals↗
PubMed2006

Refuge use: a conflict between avoiding predation and losing mass in lizards.

Prey often respond to predation risk by increasing refuge use, but this strategy may entail a loss of body condition. Factors responsible for this loss of body condition remain unclear. Also how prey deal with refuge use to cope with predation risk without incurring costs of body condition, and how initial body condition affects refuge use remain barely known. We analyzed in the field whether adult Iberolacerta cyreni lizards modify their escape strategies and refuge use in areas with different levels of habitat deterioration and ecotourism pressure, which represent different levels of predation risk, and the consequences of changes in antipredator behavior to body condition. Lizards inhabiting deteriorated areas, where risk is higher, remained closer to refuges, but decreased time spent hidden in refuges after attacks, probably to maintain similar body condition than lizards inhabiting natural areas. We performed two laboratory experiments to isolate potential costs of refuge use that might affect the body condition of male lizards: a) a decrease of the efficiency of digestion due to low temperatures inside refuges and/or b) a reduction in food intake. Results suggest that refuge use is costly in terms of body condition due to reduced food intake, but the loss of efficiency of digestion seems unimportant. Lizards modified refuge use in relation to their body condition, with lizards with worse condition decreasing time hidden after predatory attacks. We concluded that lizards compensated for increased predation risk with flexible antipredatory strategies, coping with risk without incurring costs for body condition.

Adaptation, Physiological↗
PubMed2003

Conditioning and residual emotionality effects of predator stimuli: some reflections on stress and emotion.

The advantages of using predator-related odor stimuli to study emotional responses in laboratory tests depend on whether such stimuli do elicit a relatively complete pattern of emotionality. This has been confirmed for cat fur/skin odor stimuli, which elicit a range of defensive behaviors in rats that may be reduced by anxiolytic drugs, produce residual anxiety-like behavior in the elevated plus maze and support rapid aversive conditioning to the context in which they were encountered. Although the synthetic fox fecal odor, trimethylthiazoline (TMT), elicits avoidance similar to that seen in response to cat fur/skin odor, this avoidance does not respond to anxiolytic drugs. In addition, TMT does not produce residual anxiety-like behaviors in the elevated plus maze, nor does it support conditioning. As natural cat feces also elicit avoidance but fail to support conditioning, it is possible that the ability of a predator-related odor to serve as an effective unconditioned stimulus (US) relates to its predictive status with reference to the actual presence of the predator. Avoidance per se may reflect that a stimulus is aversive but not necessarily capable of eliciting an emotional response. This view is consonant with findings in a Mouse Defense Test Battery (MDTB) measuring a wide range of defensive responses to predator exposure. A contextual defense measure that may reflect either conditioned or residual but unconditioned emotional responses was almost never reduced by drug effects unless these also reduced risk assessment or defensive threat/attack measures. However, reductions in contextual defense without changes in flight/avoidance measures were much more common. These findings suggest that flight/avoidance, although it obviously may occur as one component of a full pattern of defensive and emotional behaviors, is also somewhat separable from the others. When-as appears to be the case with TMT-it is the major or perhaps only consistent defensive behavior elicited, this may reflect a stimulus that is aversive or noxious but with little ability to predict the presence of threat or danger. That such stimuli fail to support rapid aversive conditioning suggests the need for a reanalysis of the characteristics required for an effective aversive US.

Animals↗
PubMed2000

The predator odor, TMT, displays a unique, stress-like pattern of dopaminergic and endocrinological activation in the rat.

Predator odors may provide a species relevant aversive stimuli to study the central effects of stress in rats and may have several benefits over currently applied models. Here, we examined one such odor, TMT, isolated from the fox, a predator of the rat, on fear-induced behaviors, serum corticosterone, and central dopamine metabolism. Habituated rats were exposed to TMT, or a control odor, butyric acid, in an open field. For comparison, other rats were subjected to a model of conditioned fear - a traditional fear model. Several similarities between the two stresses were observed including increased serum corticosterone and increased dopamine metabolism in the medial prefrontal cortex. Differences were also observed. TMT, but not conditioned fear, activated dopamine metabolism in the amygdala, but not the nucleus accumbens core and shell. Rats exposed to conditioned fear, but not TMT odor, demonstrated altered behaviors associated with fear, including locomotion, grooming and immobility. Finally, rats reexposed to TMT after a 24-h delay did not demonstrate any of the changes observed with acute exposure to TMT. These data indicate acute exposure to a predator odor, TMT, can result in a unique pattern of biochemical activation that is similar, but not identical, to conditioned fear. The differences may indicate unique features of a central 'fear arousal' pathway that responds to innate, unlearned stressful stimuli, such as predator odors.

Animals↗
PubMed2001

Habitat-related predation on juvenile wild-caught and hatchery-reared red drum Sciaenops ocellatus (Linnaeus).

We examined the patterns of habitat-specific mortality for newly settled red drum (Sciaenops ocellatus) using an experimental mesocosm approach. Experiments were designed to analyze prey vulnerability and fish rearing-type (wild-caught or hatchery-reared) in estuarine habitats of varying structural complexity including marsh (Spartina alterniflora Loisel), oyster reef (Crassostrea virginica Gmelin), seagrass (Halodule wrightii Aschers), and nonvegetated sand bottom. We used two different predators, pinfish (Lagodon rhomboides Linnaeus) and spotted seatrout (Cynoscion nebulosus Cuvier). For both predators, vulnerability of wild-caught red drum was significantly lower in structurally complex habitats such as seagrass and oyster reef; the highest vulnerability was associated with the nonvegetated bottom. This habitat effect was not apparent for hatchery-reared prey. In trials using a combination of both rearing-types, there was no significant habitat effect on prey selection, but hatchery-reared red drum suffered higher overall mortality than wild-caught fish from pinfish predators. In these trials, spotted seatrout did not select for either prey type. Differences we observed in prey vulnerability were likely caused by behavioral differences between wild-caught and hatchery-reared red drum. Our results reinforce the conclusion that structural complexity in estuarine habitats increases survival of newly settled fishes. Our data also suggest that hatchery-reared red drum may be more vulnerable to predation than natural fishes, and that survival of stocked fish may be enhanced through habitat-related behavior modification.

Journal Article↗
PubMed1990

N-person games and the evolution of co-operation: a model based on predator inspection in fish.

Two N-person game theoretical models examining the evolution of co-operation during predator inspection in fish are presented. Predator inspection occurs in small shoals of fish, in which one to a few individuals, the "inspectors" (co-operators) break away from the shoal and cautiously approach a predator to obtain information on this potential danger. In the models presented here, remaining with the shoal and not inspecting is considered an act of defection. Both model I and II produce a stable internal polymorphism of inspectors and noninspectors. While the equilibrial frequency of inspectors can be low (i.e. less than 10%) at large shoal size, the proportion of shoals containing any inspectors--and therefore exhibiting the inspection behavior--is much greater. Both models presented here, and N-person games in general are equivalent to intrademic group selection models of evolution in structured populations, in which shoals are trait groups and co-operation evolves by between-shoal selection. While the results are cast in terms of predator inspection, the model itself is general and applies to any multi-group scenario where co-operators benefit entire groups at their own expense. The results presented here add to the mounting theoretical and empirical evidence that co-operation is frequently not a pure evolutionarily stable strategy, and that many metapopulations should be polymorphic for both co-operators and defectors.

Animals↗