Measurement of consummatory behavior in honey bees

Consummatory behavior in honey bees can be measured by recording contact of the proboscis with sucrose solution in the food cup of an automatic feeder, and the behavior can be instrumentalized by arranging for contact of the proboscis with the food cup to activate the feeder. Illustrative free-operant and discrete-trials data are presented.     

Suppression of operant vs consummatory behavior

The magnitude and variability of conditioned suppression of bar pressing and dipper licking were compared. In two steady-state experiments, suppression of bar pressing was more profound and more stable from day to day. The two measures of suppression were uncorrelated as indexed by Pearson product-moment correlation coefficients computed for adjacent trials. Correlations within measures (internal consistency) were somewhat higher for the bar-press system except when a high proportion of rats completely suppressed on one of the correlated trials. In a transient state experiment in which possible adventitious punishment of both response systems was eliminated, suppression of bar pressing was again more profound and considerably slower to extinguish.     

Scaling relative incentive value in consummatory behavior

Surprising downshifts from more preferred (training incentive) to less preferred incentives (test incentive) are usually accompanied by emotional activation and suppression of conditioned behavior in rats. Two experiments were designed to determine whether consummatory behavior is similarly affected by downshifts of equal proportions. Within limits, the degree of consummatory responding during incentive downshift was similar with equal ratios of test concentration to training concentration. Thus, 32–4% and 16–2% downshifts (1:8 test/training ratios) caused similar levels of consummatory behavior, despite differences in the absolute concentrations of the solutions involved in the downshift. An interpretation based on sensory contrast was discarded because of the long intervals between training and test solutions (40 min and 24 h in Experiments 1 and 2, respectively). It is suggested that Weber’s law regulates behavioral suppression after reward downshifts. A theoretical framework for the interpretation of these data is presented.     

Improved techniques for the measurement of consummatory behavior in fishes

Improvements on a technique for the study of consummatory behavior and appetitive conditioning in fishes are described: a target-strike detector module easily incorporated into conventional relay programming equipment, a liquid-food formula highly attractive to goldfish and carp, a reliable Teflon-headed syringe plunger capable of handling gritty foods, and a silent food-pumping system.     

Spontaneous recovery of consummatory behavior, but not of consummatory successive negative contrast

Five experiments were designed to study spontaneous recovery (SR) in two situations involving consummatory behavior: consummatory successive negative contrast (cSNC) and consummatory extinction (cE). SR of consummatory suppression should occur if incentive downshift induces an egocentric memory encoding information about the emotional reaction to the downshift that is counterconditioned or extinguished during exposure to the downshifted reward. SR of cSNC failed to occur after resting periods of 24, 96, or 336 h interpolated following complete (Experiment 1) and incomplete (Experiment 2) recuperation of consummatory behavior, and was not induced by the opioid-receptor antagonist naloxone (2 mg/kg), known to enhance cSNC (Experiment 3). However, SR of consummatory behavior occurred across sessions in cSNC (Experiment 3) and cE (Experiments 4-5). Furthermore, naloxone facilitated cE without affecting SR (Experiments 4-5). These results are discussed in relation to evidence for the development of an egocentric memory of the aversive downshift experience in consummatory situations.     

Acoustic startle reflexes in the rat during consummatory behavior.

Auditory startle reflexes were elicited in thirsty rats when they were drinking water or were between drinking boutsmthe reaction was greater during drinking, this enhancement developing over the first few seconds after drinking onset. The startle reaction was lowest immediately after the termination of drinking. Reflex enhancement was reduced when thirsty rats drank milk rather than the more preferred water. The reflex was smaller with increased water deprivation, but enhancement produced by drinking was apparent at all levels of deprivation studied, satiety to 4-days deprivation. The inhibitory effect of a preliminary stimulus was not affected by consummatory behavior. Attention is drawn to suggestive parallels between these behavioral effects and other consequences of consummatory activity, primarily having to do with electrophysiological events and arousal processes     

Some conditions for the dissociation of consummatory and instrumental behavior in rats

To investigate whether consummatory and instrumental behavior depend upon different motivational factors, rats were trained to press a bar for saccharin solution, then given various treatments designed to reduce the palatability of saccharin, and finally tested for bar-pressing in extinction and for free intake of saccharin. Prefeeding with dextrose, prefeeding with saccharin, and association of saccharin with injections of lithium chloride all reduced intake of saccharin compared to control treatments, but only prefeeding with dextrose also reduced barpressing in extinction. Thus, performance of an instrumental response may depend upon need for food rather than appetite for it.     

Successive negative contrast after partial reinforcement in the consummatory behavior of rats

Rats given access to a 32% sucrose solution later reject a 4% solution significantly more than controls that have only received the 4% solution. In Experiment 1, this consummatory successive negative contrast (cSNC) effect was attenuated by previous exposure to 50% partial reinforcement. Furthermore, recovery from cSNC was also facilitated by partial reinforcement. In Experiment 2, the attenuating effects of partial reinforcement on cSNC were eliminated by administration of the benzodiazepine anxiolytic chlordiazepoxide (5 mg/kg) before nonreinforced trials. In Experiment 3, the attenuating effect of partial reinforcement was greater after a shift from 32 to 6% solution, than after a shift from 32 to 2% solution. The parallels between the effects of partial reinforcement on consummatory and instrumental behavior are discussed.     

Disrupted patterns of consummatory behavior in rats with fornix transections

The feeding and drinking behavior was examined in male rats with fornix transections and sham-operated control rats. Total food and water consumption was recorded but supplemented by a pattern analysis of feeding and drinking behavior. The behavior of the rats was continuously monitored during four hour morning and afternoon sessions under ad lib access and during a two hour session following adaptation to a restricted access feeding schedule. Rats with fornix transections were more active and exhibited increased frequencies of rearing, eating and drinking. The increased meal frequency in rats with fornix transections was accompanied by decreased meal durations and a reduction in the length of intermeal intervals. Total food and water consumption was unaffected by fornix transection as were the duration of sleep bouts and the frequencies of grooming, sleeping and carrying shavings. Fornix transections also reduced food carrying and food hoarding but only under conditions of restricted food access. The results suggest that fornix transection does not alter major homeostatic regulatory mechanisms nor does it alter the components of feeding and drinking behavior. Fornix transection alters, instead, the organization of microregulatory feeding and drinking patterns.     

Effect of varied taste experience on negative contrast in consummatory behavior

Rats shifted from 32% to 4% sucrose consume less 4% sucrose than animals that experience only the 4% solution. Previous experiments have suggested that a stress/emotional factor may be causally related to this negative contrast effect on the second postshift day, but not on the first postshift day. The present experiment was concerned with the possibility that contrast on the first postshift day is related to a neophobic response to the postshift solution. Results showed that giving animals experience with variously flavored (seven different flavors) 32% sucrose during the preshift period reduced degree of contrast when the animals were shifted to 4% sucrose. These data are considered in terms of solution novelty, specific loss of "sweetness", and caloric loss as contributors to negative contrast.     

Conditioning of appetitive and consummatory sexual behavior in male Japanese quail.

Two different types of stimulus objects, a live female quail artificially adorned with bright orange feathers and an inanimate toy dog, served as conditioned stimuli. For subjects in experimental groups, the conditioned stimuli were presented shortly before access to a sexually receptive normal female quail. For subjects in control groups, exposure to the conditioned stimuli was unpaired with copulatory opportunity. Subjects in the experimental but not in the control groups quickly came to approach the location of the conditioned stimulus objects. When an adorned female quail served as the conditioned stimulus, the conditioned approach behavior was controlled by a combination of the presence of the orange adornments and the visual cues of the head and neck of the female bird, and the approach behavior persisted as the adorned female moved to new locations. When the toy dog served as the conditioned stimulus, the conditioned approach behavior was limited to the spatial cues that surrounded the toy dog during conditioning trials. Although both types of stimulus objects evoked conditioned approach behavior, only the adorned female stimulus supported copulatory behavior. This last finding indicates that copulatory behavior can become redirected toward novel stimuli as a result of conditioning, but only under special circumstances. The results are consistent with the suggestion that appetitive components of reproductive behavior are more susceptible to conditioning than consummatory components. Possible reasons for this are discussed, together with implications of the results for the contribution of conditioning processes to sexual selection.     

The effects of modifying consummatory behavior on the topography of the autoshaped pecking response in pigeons

The autoshaped responses of two debeaked pigeons that had developed modified eating behavior were compared to the autoshaped responses of three control subjects that ate grain normally. The control subjects exhibited keylight responding that was judged normal by two independent raters. The debeaked subjects pecked the key and ate grain with both normal and modified responses. The results of this study demostrate that an autoshaping procedure using grain as an appetitive stimulus may be used to establish a response that is not biologically preorganized.