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At least 163 records · Page 9Linked to original sources

Species identity dominates the relationship between predator biodiversity and herbivore suppression.

Agricultural pest suppression is an important ecosystem service that may be threatened by the loss of predator diversity. This has stimulated interest in the relationship between predator biodiversity and biological control. Multiple-predator studies have shown that predators may complement or interfere with one another, but few experiments have determined if the resulting effects on prey are caused by changes in predator abundance, identity, species richness, or some combination of these factors. We experimentally isolated the effect of predator species richness on the biological control of an important agricultural pest, the green peach aphid. We found no evidence that increasing predator species richness affects aphid biological control; overall there was no strong complementarity or interference among predator species that altered the strength of aphid suppression. Instead, our experiments revealed strong effects of predator species identity, because predators varied dramatically in their per capita consumption rates. Our results are consistent with other multiple-predator studies finding strong species-identity effects and suggest that, for the biological control of aphids, conservation strategies that directly target key species will be more effective than those targeting predator biodiversity more broadly.

Animals↗

The effect of past and present group size on responses to prey in the ant Formica polyctena Först.

We investigated the responses to insect prey (dead houseflies) in 24 "derivative groups" of workers of the ant Formica polyctena created by taking sets of 25 workers out of nine larger "initial groups" kept in laboratory without queens and brood during the preceding five months. In the derivative groups the ants ceased to retrieve flies to their nests after a period ranging from few days to several weeks. The duration of that period did not depend on the present size of the derivative group (decreasing as a result of worker mortality), but was positively correlated with the estimated size of the initial group of the tested ants. The readiness to display venom spraying was higher in smaller derivative groups. These data demonstrate that responses of F. polyctena to insect prey are strongly influenced both by the present and the past size of their group.

Animals↗

Ethological studies in the ant Tetramorium caespitum Mayr. I. Foraging and building behavior.

Carrying heavy objects is a common element in the foraging and building behavior of ants. The initial stages of this behavior, i.e., lifting and moving in T. caespitum displayed as stereotyped patterns of movement. These patterns do not improve as the ants become older and more experienced, which suggest their congenital nature. Growing experience of ants is manifested in the later stages of the transportation of heavy objects, and especially in entering the correct opening of the nest with the carried prey. When a foraging ant leaves its nest to return to the prey it initially moves in the general direction of its objective. It is not until a certain distance from the nest is reached, that the ant is able to use olfactory stimuli to locate and follow its previous path. These observations indicate that the representatives of this species do not learn an exact way to and from the nest but instead have a memory for direction. The congenital character of these basic elements of foraging and building behavior allows the existence of a social organization without a division of work and foraging areas.

Animals↗

[Selection of strays from the group by predators during prey].

Equally sated three-spined sticklebacks (Gasterosteus aculeatus) that had a free view of stray individuals and of a swarm of Daphnia magna preferentially preyed upon the strays; the resulting risk to the strays increased with swarm density (a leads to c leads to e in Fig. 1). This applied also to situations with constant swarm numbers but varied density (a leads to b, d leads to e). The results from two experiments with equal swarm density (b/e, c/d) suggest selection to be affected also by swarm number and/or volume.

Animals↗

[Significance of olfaction in the feeding behavior of toads (Amphibia, Anura, Bufonidae): studies with the natterjack (Bufo calamita Laur.)].

The influence of olfactory and visual prey stimuli on the feeding behaviour of toads was studied as well as their response to lasting olfactory cues. A further aim was to find simple methods for testing olfactory responsiveness in anurans. Subjects were 8 adult specimens of the European species Bufo calamita (natterjack) kept in captivity one year at least. The results point to the rôle of olfaction in these animals.

Animals↗

[Metazoan parasites of the bluewing searobin Prionotus punctatus (Bloch, 1793) (Osteichthyes: Triglidae) from the coastal zone of the State of Rio de Janeiro, Brazil].

Eighty specimens of P. punctatus from Angra dos Reis, coastal zone of the State of Rio de Janeiro (23 degrees 01'S, 44 degrees 19'W), were necropsied between May 2002 to August 2003 to study their infracommunities of metazoan parasites. Were collected 23 species of metazoan parasites: 4 digenean, 2 monogeneans, 2 cestodes, 2 acantocephalans, 6 nematodes, 3 copepods, 2 branchiura, 1 isopod and 1 hirudinean. All fishes were parasitized by two or more parasites species. The nematodes was the predominant taxon (58.6% of parasites collected). Hysterothylacium sp. was the most prevalent, abundant and dominant species. The total of parasites collected and the parasites species richness were significantly correlated with host's total length. Ten species of parasites showed significantly correlation between parasites abundance and total length of P. punctatus. The sex of the host showed positive influence on abundance and prevalence of Hysterothylacium sp., Progrillotia dollfusi Carvajal and Rego, 1983 and Dolops sp. Four pairs of adult endoparasites, one pair of endoparasites larval stages and two pairs of ectoparasites presented association and/or covariation between its prevalences and abundances, respectively. Quantitative dominance of endoparasites in the parasite community of P. punctatus could be related with the predatorious behavior of this fish.

Animals↗

Effects of environmental conditions and prey size on locomotion behaviors of planktivorous fish.

The locomotion behavior of Pseudorasbora parva was observed in laboratory under various light intensity, turbidity, structural complexity and zooplankton size, focusing on swimming speed and time of search, approach, and attack. At low prey density, the satiation level affected the swimming speed only slightly. The search speed was nearly constant regardless of the satiation level to reduce the swimming energetic cost when opportunities of encountering prey were low. However, the attack and approach speeds slightly decreased with satiation. With increasing visual and swimming conditions, the approach speed increased markedly, but the search and attack speeds did not. Although the time for the approach and attack to capture a prey did not change much with decreasing swimming and visual conditions, the search time significantly increased to compensate for the decreased swimming speed.

Animals↗

Neuronal elements that mediate escape swimming and suppress feeding behavior in the predatory sea slug Pleurobranchaea.

1. The white, bilaterally paired A1 interneurons of the cerebropleural ganglion of Pleurobranchaea californica fire rhythmic bursts of action potentials during escape swimming behavior. We studied the role of the A1s in swimming behavior and pattern generation in whole animal and isolated CNS preparations. 2. The escape swim is a cyclic sequence of dorsal and ventral flexions of the body. During the swim, A1 bursts precede and accompany the dorsal flexion phase of the cycle. Hyperpolarization of A1 to prevent spike activity interrupts swimming behavior in the whole animal and fictive swimming in the isolated CNS. Stimulated A1 activity was not observed to cause swimming in whole animals, and was only occasionally sufficient to trigger fictive swimming activity in the isolated CNS. 3. In quiescent whole animal preparations, stimulation of a single A1 normally causes a single dorsal flexion followed by body flexion to the side contralateral to the stimulated cell; characteristically, A1 spike activity stimulates feedback inhibition coinciding with the end of dorsal flexion and the onset of contralateral flexion. 4. A1 spike activity suppresses feeding behavior and causes proboscis retraction in whole animal preparations induced to feed. A1 activity also suppresses fictive feeding driven by stimulation of the critical phasic paracerebral neurons (PCps) of the motor network of feeding in the isolated CNS. Concomitantly, A1 spikes cause potent inhibition of the PCp interneurons. 5. The A1s are specifically excited by noxious mechanical and chemical stimuli, but are not affected by feeding stimuli or the occurrence of feeding behavior. 6. We conclude that the A1 neurons are elements of an escape swimming pattern generator, and that they are probably homologous to the similar C2 neurons of the nudibranch Tritonia diomedea. One of their functions outside of generating the swim pattern may be the suppression of feeding behavior in response to noxious stimulation. These observations provide a neural mechanism for the original observations of the dominance of escape swimming behavior over feeding.

Action Potentials↗

Cost-benefit analysis potential in feeding behavior of a predatory snail by integration of hunger, taste, and pain.

Hunger/satiation state interacts with appetitive and noxious stimuli to determine feeding and avoidance responses. In the predatory marine snail Pleurobranchaea californica, food chemostimuli induced proboscis extension and biting at concentration thresholds that varied directly with satiation state. However, food stimuli also tended to elicit avoidance behavior (withdrawal and avoidance turns) at concentration thresholds that were relatively low and fixed. When the feeding threshold for active feeding (proboscis extension with biting) was exceeded, ongoing avoidance and locomotion were interrupted and suppressed. Noxious chemostimuli usually stimulated avoidance, but, in animals with lower feeding thresholds for food stimuli, they often elicited feeding behavior. Thus, sensory pathways mediating appetitive and noxious stimuli may have dual access to neural networks of feeding and avoidance behavior, but their final effects are regulated by satiation state. These observations suggest that a simple cost-benefit computation regulates behavioral switching in the animal's foraging behavior, where food stimuli above or below the incentive level for feeding tend to induce feeding or avoidance, respectively. This decision mechanism can weigh the animal's need for nutrients against the potential risk from other predators and the cost of relative energy outlay in an attack on prey. Stimulation of orienting and attack by low-level noxious stimuli in the hungriest animals may reflect risk-taking that can enhance prey capture success. A simple, hedonically structured neural network model captures this computation.

Animals↗

Phagocytic behavior of the predatory slime mold, Dictyostelium caveatum. Cell nibbling.

The predatory slime mold, D. caveatum, feeds upon other amoebae by phagocytosis. The D. caveatum amoebae begin feeding upon cells the same size or larger by nibbling pieces of cells. While feeding upon other amoebae as opposed to bacteria, they increase in size. This behavior resembles that of phagocytes in higher organisms. A novel method was used to follow the time course of phagocytosis. A lytic toxin, phallolysin, and mutants resistant to the toxin were utilized in an assay to separate the phagocytes from the prey cells. Since a broad spectrum of cells are sensitive to the toxin, the method has general applicability.

Amanitins↗

Defensive behavior in rats towards predatory odors: a review.

Studies of the response of rodents to predatory odors (mainly cat) have provided useful insights into the nature of defensive behavior. This article reviews work in this area with a focus on a behavioral paradigm recently developed in our laboratory in which we present rats with a piece of fabric collar that has been previously worn by a cat. Rats presented with this stimulus spent most of their time engaged in a behavior we call 'head out' in which the rat pokes its head out from a hide box and scans the environment. Periodic 'flat back approaches' and 'vigilant rearing' towards the cat odor source are seen as well as inhibition of non-defensive behaviors such as locomotor activity and grooming. Cat odor causes a sustained increase in blood pressure (> 15mm Hg) without greatly affecting heart beat rate. Rats will develop conditioned fear to both contexts and cues that have been paired with cat odor. C-fos immunohistochemistry indicates that cat odor selectively activates a defensive behavior circuit involving the medial amygdala, ventromedial and dorsomedial hypothalamus, dorsal premammillary nucleus and the periaqueductal gray. The defensive response to cat odor is attenuated by acute administration of the benzodiazepine midazolam (0.375 mg/kg), with chronically administered SSRI antidepressants and acute alcohol exerting more modest anxiolytic effects. The behavioral response to cat odor is very different to that seen to trimethylthiazoline (TMT: fox odor) which has effects more like those seen to an aversive putrid odor. It is concluded that cat odor is a useful tool for elucidating behavioral, neural, pharmacological and autonomic aspects of defensive behavior and anxiety.

Aggression↗

GABA receptor mediated suppression of defensive rage behavior elicited from the medial hypothalamus of the cat: role of the lateral hypothalamus.

Recently, our laboratory has demonstrated that predatory attack behavior in the cat, elicited by electrical stimulation of the lateral hypothalamus, is suppressed following activation of the region of the medial hypothalamus from which defensive rage behavior is elicited [Han, Y., Shaikh, M.B., Siegel, A., Medical amygdaloid suppression of predatory attack behavior in the cat: II. Role of a GABAergic pathway from the medial to the lateral hypothalamus, Brain Res., 716 (1996) 72-83.]. The mechanism for this suppression is a direct GABAergic projection from the medial to lateral hypothalamus. The present study tested the hypothesis that the inhibitory relationship between these two regions of hypothalamus is reciprocal, namely, that a GABAergic neuron, which also projects from the lateral to medial hypothalamus, serves to suppress defensive rage elicited from the medial hypothalamus. Monopolar stimulating electrodes were implanted into lateral hypothalamic sites from which predatory attack behavior was elicited. In addition, cannula-electrodes were implanted into the medial hypothalamus for elicitation of defensive rage behavior and for microinjections of GABA compounds. Initially, in the absence of drug administration, the effects of dual stimulation of the lateral and medial hypothalamus upon response latencies were compared with those following single stimulation of the medial hypothalamus alone. Dual stimulation significantly (p<0.01) suppressed defensive rage behavior elicited from the medial hypothalamus. Then, administration of the GABAA receptor antagonist, bicuculline (10-60 pmol), into medial hypothalamic sites from which defensive rage was elicited blocked the suppressive effects of lateral hypothalamic stimulation. The GABAA receptor agonist, muscimol (0.3-30 pmol), microinjected into the medial hypothalamus, suppressed defensive rage elicited by single stimulation of the medial hypothalamus in a dose dependent manner. These suppressive effects of muscimol upon defensive rage were blocked following pretreatment with bicuculline (60 pmol). Administration of muscimol into adjoining regions of the lateral hypothalamus had no effect upon defensive rage, indicating its site specificity. Bicuculline (60 pmol) delivery into the medial hypothalamus had no effect upon defensive rage, suggesting the, presence of a phasic rather than tonic mechanism. A combination of immunocytochemical and retro grade tracing procedures were then employed to determine the origin of the putative GABAergic pathway projecting to the medial hypothalamus. In this experiment, the retrograde tracer, Fluoro-Gold (8%, 0.5 microl), was microinjected through a cannula-electrode in the medial hypothalamus from which defensive rage had been elicited. Following survival periods of 5-6 days, cats were perfused with 4% paraformaldehyde and brain tissue was processed for immunocytochemical staining of GABA neurons. Retrogradely labeled, immunopositively labeled, as well as Fluoro-Gold and GABA labeled cells, were identified in the lateral hypothalamus. Each type of neuron was distributed over wide regions of the lateral hypothalamus, extending from the area immediately caudal to the optic chiasm to the level of the posterior hypothalamus. Together, the behavioral pharmacological and anatomical data provide evidence of a direct inhibitory projection from the lateral to medial hypothalamus whose functions are mediated by GABAA receptors. When coupled with our previous findings, these results reveal the presence of reciprocal GABAergic inhibitory pathways between the medial and lateral hypothalamus. The findings suggest that functions associated with either the lateral or medial hypothalamus, but not both, can be activated at a given time.

Aggression↗

Brain structures and neurotransmitters regulating aggression in cats: implications for human aggression.

1. Violence and aggression are major public health problems. 2. The authors have used techniques of electrical brain stimulation, anatomical-immunohistochemical techniques, and behavioral pharmacology to investigate the neural systems and circuits underlying aggressive behavior in the cat. 3. The medial hypothalamus and midbrain periaqueductal gray are the most important structures mediating defensive rage behavior, and the perifornical lateral hypothalamus clearly mediates predatory attack behavior. The hippocampus, amygdala, bed nucleus of the stria terminalis, septal area, cingulate gyrus, and prefrontal cortex project to these structures directly or indirectly and thus can modulate the intensity of attack and rage. 4. Evidence suggests that several neurotransmitters facilitate defensive rage within the PAG and medial hypothalamus, including glutamate, Substance P, and cholecystokinin, and that opioid peptides suppress it; these effects usually depend on the subtype of receptor that is activated. 5. A key recent discovery was a GABAergic projection that may underlie the often-observed reciprocally inhibitory relationship between these two forms of aggression. 6. Recently, Substance P has come under scrutiny as a possible key neurotransmitter involved in defensive rage, and the mechanism by which it plays a role in aggression and rage is under investigation. 7. It is hoped that this line of research will provide a better understanding of the neural mechanisms and substrates regulating aggression and rage and thus establish a rational basis for treatment of disorders associated with these forms of aggression.

Aggression↗