Differences in the responses of identified neurons to chemical stimuli in satiated and hungry edible snails

Reactions of command neurones for avoidance behaviour to food were investigated in hungry and satiated snails in "CNS-chemoreceptor" preparations, in which hemolymph was washed out by saline. Neuronal responses in hungry animal preparations differed significantly from responses in satiated animals preparations. Perfusion of hungry animal preparations with hemolymph of satiated animals changed significantly the responses of command neurones for avoidance behaviour. These responses resembled the reactions of the same neurones to food after aversive conditioning to food of hungry snails. The role of humoral factor in learning is discussed.     

Assessing Projection Bias in Consumers’ Food Preferences

The aim of this study is to test whether projection bias exists in consumers’ purchasing decisions for food products. To achieve our aim, we used a non-hypothetical experiment (i.e., experimental auction), where hungry and non-hungry participants were incentivized to reveal their willingness to pay (WTP). The results confirm the existence of projection bias when consumers made their decisions on food products. In particular, projection bias existed because currently hungry participants were willing to pay a higher price premium for cheeses than satiated ones, both in hungry and satiated future states. Moreover, participants overvalued the food product more when they were delivered in the future hungry condition than in the satiated one. Our study provides clear, quantitative and meaningful evidence of projection bias because our findings are based on economic valuation of food preferences. Indeed, the strength of this study is that findings are expressed in terms of willingness to pay which is an interpretable amount of money.     

Effects of Hunger on Foraging Behavior of Age-0 Smallmouth Bass in a Heterogeneous Environment

We examined how hunger affected habitat use by juvenile smallmouth bass, Micropterus dolomieu, as they moved among a variety of habitat patches. Hungry and satiated fish were placed in an artificial stream that contained three types of habitat patches: pools with uniform depth and low water velocities, mazes with uniform depth and moderate water velocities, and riffle-pool complexes with varying depth and the highest water velocities. Food was only available in the riffle-pool complexes. Hungry fish spent more time in the riffle-pool complex than satiated fish did. However, hungry and satiated fish did not differ in the time it took to exit the pool they were initially placed in, the number of patches entered, or the number of times they moved among patches. Both hungry and satiated fish frequently entered other patches after foraging successfully in the riffle-pool complexes. There was wide variation in foraging behavior among individuals in both treatment groups, and we consistently observed individuals that did not alter their foraging behavior in response to the difference in food availability among patches.     

A shift in prey color preference in the green toad Bufo viridis Laur. after food satiation]

In the behavioural experiments when showing simultaneously coloured stimuli (food targets) and also in choosing between two stimuli, red and blue, it had been shown with a high level of reliability that the hungry Bufo viridis which had not been fed for at least a week, in the overwhelming majority of cases chose the red-coloured food targets. Within 1-3 days after an abundant feeding, in the same animals the changes occurred in their preferences of the prey colour. The percentage of choosing the blue targets by the satiated toads significantly increases. In a separate series of experiments had been demonstrated that the changing motivation is conditioned by colour, since hungry and satiated Bufo viridis under conditions of simultaneous demonstration of four stimuli, black and three different grey stimuli, chose exclusively the black stimulus.     

Alteration of thermoregulation behavior in juvenile fish in relation to satiation level

Thermoregulation behavior of satiated and hungry juvenile sterlet Acipenser ruthenus, the Siberian sturgeon Acipenser baeri, and the goldfish Carassius auratus was studied. Significant alterations of thermoregulation behavior appear in juvenile fish one day after food deprivation. Hungry fish preferred, on average, lower temperatures, their temperature range was broader, and the locomotor activity was higher than in satiated fish.     

Discriminating between Hungry and Satiated Predators: The Response of Guppies (Poecilia reticulata) from High and Low Predation Sites1

Fixed anti-predator activities are costly because they limit the ability of the prey to take advantage of short term temporal patchiness in predation pressure. The ability to discriminate between hungry and satiated predators and a flexible response to the differential threat can help to lower the costs of anti-predator behavior. In this study Trinidadian guppies (Poecilia reticulata) were found to distinguish between hungry and satiated predators. In Trinidad, populations of guppies experience different levels of predation from piscivorous fish. Individuals taken from populations with chronically high predation pressure responded stronger to the hungry predator than those from low predation sites.     

The Effect of Predator Hunger on Chemically Mediated Antipredator Responses and Survival in the Wolf Spider Pardosa milvina (Araneae: Lycosidae)

The wolf spider Pardosa milvina exhibits effective antipredator behavior (reduced movement) in the presence of silk and excreta from a larger co‐occurring predatory wolf spider Hogna helluo. As the quantity and quality of the silk and excreta may vary with the hunger state of the predator, we tested if chemical cues from a hungry vs. satiated H. helluo affected the activity level and survival of P. milvina. Pardosa milvina response was measured on substrates containing chemical cues from (1) a satiated H. helluo, (2) a H. helluo that had been withheld food for 2 wk, (3) cues from adult domestic crickets (Acheta domesticus), or (4) a blank test substrate (20 replicates/treatment). Pardosa milvina activity level was recorded on each substrate over a 30‐min period using video‐tracking equipment (Videomex‐I^®; Columbus Instruments, Columbus, OH, USA). We then measured P. milvina survival in the presence of hungry or satiated H. helluo on cues from a hungry H. helluo, satiated H. helluo, or a blank control (2 × 3 design). Pardosa milvina significantly reduced activity in the presence of H. helluo cues and showed significantly less activity in the presence of cues from a hungry H. helluo compared with a satiated one. Cue type and predator hunger state significantly affected P. milvina survival in the presence of live predators. However, cues from hungry vs. satiated H. helluo resulted in no difference in P. milvina survival. Pardosa milvina can discriminate between hungry vs. satiated predators based on silk and excreta cues alone, but differences in behavior as a result of this discrimination did not translate into increased survival in the presence of a live predator.     

Responses of Acilius sulcatus (Coleoptera: Dytiscidae) to chemical cues from perch (Perca fluviatilis)

In this study we tested the hypothesis that the presence of chemical stimuli from a hungry predator would initiate anti-predator responses, while stimuli from a satiated predator would not. We used chemical stimuli released from starved perch (Perca fluviatilis) and from satiated perch (predator). As prey we used adult Acilius sulcatus (Coleoptera: Dytiscidae). The reaction of the beetles to different predator conditions was tested during daytime. We also tested the reaction to starved perch during the night. A. sulcatus activity decreased when it was exposed to stimuli released from starved perch during daytime when visibility was poor, due to the presence of artificial vegetation. There was, however, no reaction to satiated perch under the same experimental conditions. These results indicate that A. sulcatus can discriminate between chemical cues from hungry and satiated fish predators. When visibility was good and the concentration of chemical cues was constant, the beetles did not react to starved perch in the daytime, but their activity decreased at night in response to stimuli released from starved perch. Visual as well as chemical cues seem to be important for detecting a potential predator. When visibility is good, beetles seem to rely on visual stimuli, while in darkness they seem to use chemical stimuli to detect the presence of predators. Received: 4 October 1996 / Accepted: 7 February 1997     

Cleaner fish use tactile dancing behavior as a preconflict management strategy

The most commonly asked question about cooperative interactions is how they are maintained when cheating is theoretically more profitable. In cleaning interactions, where cleaners remove parasites from apparently cooperating clients, the classical question asked is why cleaner fish can clean piscivorous client fish without being eaten, a problem Trivers used to explain reciprocal altruism. Trivers suggested that predators refrain from eating cleaners only when the repeated removal of parasites by a particular cleaner results in a greater benefit than eating the cleaner. Although several theoretical models have examined cheating behavior in clients, no empirical tests have been done (but see Darcy ). It has been observed that cleaners are susceptible to predation. Thus, cleaners should have evolved strategies to avoid conflict or being eaten. In primates, conflicts are often resolved with conflict or preconflict management behavior. Here, I show that cleaner fish tactically stimulate clients while swimming in an oscillating "dancing" manner (tactile dancing) more when exposed to hungry piscivorous clients than satiated ones, regardless of the client's parasite load. Tactile dancing thus may function as a preconflict management strategy that enables cleaner fish to avoid conflict with potentially "dangerous" clients.     

Species richness along multiple gradients: testing a general multivariate model in oak savannas

Behavioral responses of prey to their predators can critically alter community dynamics. Whether or not a prey responds, clearly depends on the effectiveness of that response. The effectiveness on the other hand is predicted to depend on predator behavior. Actively searching predators can render the behavioral responses in their prey ineffective. Nevertheless, most studies investigating the optimal reaction of prey treated predators as immobile elements of the environment. I experimentally manipulated activity of poolfrog ( Rana lessonae ) tadpoles by keeping them at low and high food levels, and exposed them to three species of invertebrate predators ( Aeshna cyanea, Anax imperator , and Dytiscus marginalis ), whose activity also was manipulated through different food levels. Satiated, less active predators were more likely to kill hungry, more active tadpoles, but hungry predators killed hungry and satiated tadpoles about equally often. This result suggests that reducing their activity is a more effective strategy for tadpoles if the predators themselves are less active. On the other hand, against hungry, highly motivated predators, the behavioral avoidance strategies were essentially ineffective. Antipredator behavior is generally thought to stabilize the dynamics of predator–prey systems. The results presented here, however, suggest that the community dynamical consequences of antipredator behavior also critically depend on decisions made by predators.     

The Effect of Feeding History on Prey Capture Behaviour in the Orbweb Spider Argiope keyserlingi Karsch (Araneae: Araneidae)

The prey capture behaviour of the orb-web spider Argiope keyserlingi Karsch was examined experimentally by subjecting spiders to two different feeding regimes (food deprived and food satiated) and three types of prey: Drosophila, blowflies (Lucilia cuprina) and bees (Apis mellifera). The attack behaviour of the spiders was influenced by both their foraging history and the type of prey. Food deprived spiders attacked Drosophila and bees more frequently than food satiated spiders, and food satiated spiders travelled more slowly to any of the prey types than food deprived spiders. Furthermore, Drosophila were never wrapped in silk but only grasped with the chelicerae, whereas both blowflies and bees were always wrapped. This provides experimental confirmation that feeding history affects the decision of orb-web spiders to accept or reject any given prey.     

Food allocation in crimson rosella broods: parents differ in their responses to chick hunger

Food allocation in many asynchronously hatching bird species favours large, competitively superior chicks. In contrast, food is usually distributed equally within broods of crimson rosellas, Platycercus elegans, implying that parents do not simply feed the most competitive chick. We used two temporary removal experiments to manipulate hunger of: (1) individual first- or last-hatched chicks, or (2) the whole brood. When only a single chick was hungry, parents compensated fully and chicks gained the same mass over the day as during controls. Mothers and fathers, however, responded in different ways to chick hunger. Mothers did not strongly alter their food allocation when a single chick was hungry, and controlled the distribution of food by refusing to feed first-hatched chicks when they were hungry and by moving more during feeds. In contrast, fathers allocated more food to hungry last-hatched chicks. When the whole brood was hungry, parents were unable to compensate chicks and all chicks lost mass over the day. In these conditions, mothers preferentially fed first-hatched chicks, while fathers fed all chicks equally. Our results show that both mothers and fathers were able to discriminate and selectively feed chicks, but that parents responded differently to changes in chick hunger within the brood. Fathers responded more strongly to variation in chick hunger within the brood, suggesting they reallocate food based on short-term changes in hunger. Mothers distributed food preferentially to last-hatched chicks except when the whole brood was hungry, when they switched to favouring first-hatched chicks. This pattern is consistent with a strategy of adaptive brood reduction when food is scarce. Copyright 2000 The Association for the Study of Animal Behaviour.     

Temporal partitioning and aggression among foragers: modeling the effects of stochasticity and individual state

In many natural systems, individuals compete with conspecificsand heterospecifics for food and in some cases, individualshave been observed to partition their foraging times or fightover food. In this study, I investigated when it is optimalfor a consumer to partition time and be aggressive. I formulatedan individual-based model of foraging and used game theoryto find evolutionarily stable strategies (ESSs) that maximizethe probability that consumers survive each day and acquiretheir daily food requirements. Consumers choose when to forageand when to behave aggressively during confrontations overfood. Consumers are each associated with a state variable,representing the amount of food eaten, and a dominance ranking, which describes how likely they are to forage and fight forfood. The ESS is sensitive to food abundance, consumer state,and the dominance ranking. When food is abundant, temporalpartitioning is often an ESS where the dominant consumer foragesfirst; however, partitioning is unlikely to be an ESS when food abundance is low. Fights over food are typically avoidedbut may be part of an ESS when food abundance is low, bothconsumers are hungry, or the time available for foraging eachday is drawing to a close. Because the ESS is sensitive toconsumer state, the stochastic nature of finding food often results in considerable variation in observed foraging dynamicsfrom one day to the next, even when consumers adopt the samestate-dependent strategy each day. Results are compared withempirical observations, and I discuss implications for consumercoexistence.     

Cleaner shrimp use a rocking dance to advertise cleaning service to clients

Signals transmit information to receivers about sender attributes, increase the fitness of both parties, and are selected for in cooperative interactions between species to reduce conflict [1, 2]. Marine cleaning interactions are known for stereotyped behaviors [3-6] that likely serve as signals. For example, "dancing" and "tactile dancing" in cleaner fish may serve to advertise cleaning services to client fish [7] and manipulate client behavior [8], respectively. Cleaner shrimp clean fish [9], yet are cryptic in comparison to cleaner fish. Signals, therefore, are likely essential for cleaner shrimp to attract clients. Here, we show that the yellow-beaked cleaner shrimp [10] Urocaridella sp. c [11] uses a stereotypical side-to-side movement, or "rocking dance," while approaching potential client fish in the water column. This dance was followed by a cleaning interaction with the client 100% of the time. Hungry cleaner shrimp, which are more willing to clean than satiated ones [12], spent more time rocking and in closer proximity to clients Cephalopholis cyanostigma than satiated ones, and when given a choice, clients preferred hungry, rocking shrimp. The rocking dance therefore influenced client behavior and, thus, appears to function as a signal to advertise the presence of cleaner shrimp to potential clients.     

Interconnection between parameters of motor activity and blood glucose concentration in newborn rats at starvation and under glucose load conditions

The study is carried out on the one-, 3-, 5-, 7, and l0-day old free moving or loosely fixed rat pups (P1–10). In satiated and submitted to the 24-h starvation rat pups, parameters of spontaneous periodical motor activity (SPMA) and the blood glucose content were determined. The total glucose level in hungry rat pups was, on average, 1.5–2.5 times lower than in satiated animals. Administration of glucose to hungry rat pups increased 6–11 times its concentration in blood as compared with the animals not obtaining glucose. The glucose administration to the satiated rat pups led to a rise of its level in blood from 2 to 5 times as compared with intact animals, which was 2–3 times less than in the case of hungry animals. Analysis of pattern of motor activity recorded under conditions of the glucose deficit caused by the 24-h starvation of rat pups did not reveal significant changes of ratio of rhythmical components. Introduction of glucose to hungry and to the lesser degree to satiated rat pups led to potentiation of the minute rhythm of activity in all age groups. The exception was the first day after birth when the glucose administration to satiated rat pups promoted an enhancement of the decasecond rhythm and a decrease of the total level of motor activity. Comparison of ontogenetic dynamics of the SPMA parameters and the glucose content in blood of hungry rat pups revealed the clearly expressed regularity absent in the satiated animals: the glucose level in blood was higher during activity than in the state of rest. The performed study has shown that intensity, duration, and, to a degree, pattern of SPMA in the newborn rat pups depend on the level of satiety, and can be significantly changed in the artificially produced hypo- or hyperglycemia. The existing ontogenetic fluctuations in the character of reaction at performance of the glucose tolerance test can be connected both with morphofunctional maturation of the motor system and with immaturity of various chains of carbohydrate metabolism.     

Food selection, food-seeking patterns and hunting success of captive Goosanders Mergus merganser and Red-breasted Mergansers M. serrator in relation to the behaviour of their prey

Food selection and food-seeking behaviour of hand-raised Goosanders Mergus merganser and Red-breasted Mergansers M. serrator were tested in experimental situations. When different combinations of two species of fish were presented simultaneously to hungry birds in a small trough where the prey was easily and equally available, neither duck species showed any preferences in prey selection. However, when these same fish species were presented to satiated birds, they showed definite preferences; the most preferred species were baltic salmon and brown trout followed in decreasing order by minnow, whitefish, sculpin, burbot and river lamprey. This was also the case when combinations of five to seven species were presented. However, under semi-natural conditions in a stream tank, the number of each species offish caught was related to their escape behaviour, not to the previously determined predator preferences. When salmon and minnows of different size were presented to hungry birds, they selected the larger fish regardless of species. In contrast, when satiated, they preferred small fish over large fish. Under the experimental conditions, the use of certain elements of foraging behaviour clearly differed between the two bird species: Mergus serrator spent more time hunting underwater than did M. merganser. Results are discussed in relation to the predator-prey situation existing under natural conditions in northern Swedish rivers.     

The facilitation of defensive reactions during food consumption in the snail helix: the participation of glucose and gastrin/cholecystokinin-like peptide]

Molecular and cellular mechanisms of the interrelations between the feeding and defense behaviour were studied in a snail Helix lucorum. The dynamics of defense reactions was investigated in snails with different levels of feeding motivation. Defense reactions were suppressed in hungry snails, while 15-20 min after the beginning of food intake they were facilitated. The facilitation depended on a duration of starvation. Injection of 0.5 ml of 5 mM glucose solution (up to the glucose level in the haemolymph of a food satiated snail, 1.6-2.0 mM) or injections of 20-30 ng of synthetic analogues of the gastrointestinal peptides (pentagastrin of octapeptide cholecystokinin, CCK-8) facilitated the defense reaction in a hungry snail. Parameters of the facilitation were similar to those in the period of food intake. Activity of the command neurons of defense behaviour (L-PPL1) after the carrot juice application to the lip of a semi-intact preparation from a hungry snail was glucose-dependent. Similar glucose-dependent changes of L-PPL1 activity were found after CCK-8, but not FMRFamide application during the perfusion with 0.5 mM glucose. L-PPL1, but not L-PPa2-3 neurons were most sensitive to glucose and CCK-8 level changes in the Ringer solution. Adaptive significance of the behavioural phenomena as well as glucose and gastrin/CCK-like peptide participation in these processes are discussed.     

Acid-Base Balance Modulates Respiratory and Alimentary Behavior of the Mollusc Lymnaea stagnalis

An active reaction (change of pH) in hemolymph of the freshwater pulmonate mollusc Lymnaea stagnalis is studied in various physiological states: hunger, satiety, and alimentary excitation. In satiated animals the hemolymph pH is shifted to the acid area (7.6 ± 0.003) as compared with hungry animals (7.9 ± 0.05). The satiated individuals are characterized by an increased respiratory activity and decreased food consumption as compared with hungry animals. Acidification of the medium leads to an increase of excitability of the respiratory network interneurons (RPeD1, VD4, VD1/RPD2) and to inhibition of activity of the alimentary network interneurons (R/L CGC), whereas alkalization, to opposite effects. It is suggested that pH is one of factors coordinating activity of functional systems of Lymnaea stagnalis due to effect on neuronal correlates of the respiratory and alimentary behavior.     

The influence of social hunger on food distribution and its implications for disease transmission in a honeybee colony

Social insect colonies are characterized by extensive interactions among individuals, exchanges that can also potentially transmit pathogens. The large majority of these social interactions in a honeybee colony result from food transfer among individuals. Since colony hunger is likely to have a significant influence on these interactions, we investigated its effect on the distribution of food within the colony. By pulsing two colonies having different amounts of stored food with a radioactive label, we found that a starved colony sent out a larger number of foragers, brought in more food, and stored more of it than the satiated colony. We also found that the food brought into a starved colony was distributed more uniformly within each age class than that in the satiated colony. The queen and the young individuals received the lowest exposure to the label even though the label entered different regions of the colony at the same rate. The satiation level of the colony did not influence the relative exposures of different age groups to the label but a higher amount of it was stored in the hungry colony. We discuss the significance of these results in terms of the role played by the organizational structure of the honeybee colony on the transmission dynamics of an infectious disease.     

A game-theoretic model of kleptoparasitic behavior in polymorphic populations

Kleptoparasitism, the stealing of food by one animal from another, is a widespread biological phenomenon. In this paper we build upon earlier models to investigate a population of conspecifics involved in foraging and, potentially, kleptoparasitism. We assume that the population is composed of four types of individuals, according to their strategic choices when faced with an opportunity to steal and to resist an attack. The fitness of each type of individual depends upon various natural parameters, for example food density, the handling time of a food item and the probability of mounting a successful attack against resistance, as well as the choices that they make. We find the evolutionarily stable strategies (ESSs) for all parameter combinations and show that there are six possible ESSs, four pure and two mixtures of two strategies, that can occur. We show that there is always at least one ESS, and sometimes two or three. We further investigate the influence of the different parameters on when each type of solution occurs.