Increasing the rate of ethanol consumption in food- and water-satiated rats

The effecrs of food satiation, ethanol concentration and the schedule ofethanol availability on the rate ofethanol consumplion were investigated in rats. In Experiment I separate groups were exposed to 6.2 or l2.5% w/v ethanol and unlimited access to food. The food and ethanol were available concurrently for one to three hours daily. After approximately l5 sessions unlimited food was available whenever ethanol was not available. The rate of ethanol consumption was positively related to ethanol concentration and negatively related to duration of ethanol availability. In Experiment 2 similar procedures were followed. except rats had unlimited access to food throughout the experiment. The results were similar to Experiment 1. In Experiment 3 separate groups were exposed to 6.2 and 12.5%\u27 w/v ethanol for one hour every other day unlimited food was available throughout the experiment. The results were similar to the one-hour availability groups in Experiments 1 and 2. In all experiments ethanol consumption rates increased to levels above baseline and above the usuaì ethanol metabolic rate found in rats. The results demonstrated new combinations ofethanol availability and non-availability durations thal were sufficient to significantly increase the rate of ethanol consumption

Cross-modal transfer of stimulus control in the albino rat: A stimulus delay procedure

The present experiment demonstrated in a simultaneous discrete trial discrimination that the stimulus control of a rat’s leverpress response can be errorlessly transferred across stimulus modalities, i.e., from light to click location and from click to light location. Subsequent to acquisition of the original discrimination, the original and new discriminative stimuli were simultaneously presented for several sessions. Then the new discriminative stimulus was presented 3 sec prior to the onset of the original discriminative stimulus. Within the direction of transfer, e.g., from light to click location, the delay group emitted fewer trial and intertrial errors than the control group. As the new discriminative stimuli acquired control over responding, the response latency distributions were differentially affected. The results suggest that the transfer of control from the original to the new discriminative stimuli is mediated by the temporal aspects of the delay interval

Patterns of ethanol consumption as a function of schedule of ethanol access

The present experiment demonstrated that patterns of ethanol consumption can be controlled by altering the schedule of ethanol availability. Thirty-two male albino rats, maintained at 80% of their ad libitum weight, were first exposed to 10 base-line sessions in which access to either 8 or 32% ethanol was unrestricted. Each subject was then exposed to one of four restricted access schedules for 30 sessions. During each 23-hr session, the ethanol access period was held constant at 20 min while the time between ethanol access periods was either 70, 160, 340 or 700 min. After restricted access, all subjects were returned to unrestricted access for 10 sessions. Water was continually available throughout the experiment. When ethanol access periods occurred every 70 or 160 min, animals at both concentrations consumed more ethanol (grams per kilogram) than during the initial period of unrestricted access. When the time between ethanol access periods was 340 or 700 min, animals consumed an equal amount or half as much, respectively, as during unrestricted access. Analysis of responding revealed that the mean amount of ethanol consumed per bout was greater during restricted than during unrestricted access. The longer the time between access periods the greater the amount consumed per bout. Upon return to unrestricted access, total daily consumption increased, but the amount consumed per bout decreased to base-line level

Time allocation in concurrent schedules: the effect of signalled reinforcement

The responses of five pigeons were reinforced on concurrent variable-interval variable-interval reinforcement schedules in which changeover key responses changed the stimulus and reinforcement schedules associated with the food key. While the reinforcement availability in one component remained unchanged throughout the experiment, the reinforcement availability in the other component was, during several conditions, signalled by the onset of an additional discriminative stimulus. During unsignalled conditions, both the relative frequency of responding and the relative time spent in each component approximated the obtained relative reinforcement frequency in each component. The effect of signalling reinforcer availability in one component was to (1) reduce responding in the signalled component to near-zero levels, and (2) increase the relative time in the unsignalled component, without a corresponding increase in the obtained relative reinforcement frequency. The magnitude of the increase in relative time in the unsignalled component decreased as the overall frequency of reinforcement increased. This deviation in the matching relation between relative time and the obtained relative reinforcement frequency was eliminated if the overall reinforcement frequency was increased before the signal was introduced and then, without removing the signal, gradually reduced

Control of responding during stimuli that precede transitions in reinforcement frequency

Pigeons' responses were reinforced on a variant of a mixed variable-interval extinction schedule of reinforcement in which the transition to the higher reinforcement rate was signaled by a trace stimulus projected on the response key prior to the onset of the component correlated with food delivery. In the first of two experiments, the duration of the trace stimulus preceding the component correlated with food delivery was varied from 1.5 to 50.0 s and in the second experiment, the reinforcement frequency in the same component was varied from 10 to 60 reinforcers per hour. Pigeons pecked at the trace stimulus preceding the onset of the component correlated with food delivery even though responding was not reinforced in its presence and only one of the changes in reinforcement rate (i.e., from extinction to reinforcement) was signaled. The rate of pecking during the trace stimulus was a function of its duration but not of the reinforcement frequency in the following component. Higher rates generally occurred at the shorter trace-stimulus durations. Component responding following the offset of the trace stimulus was under discriminative control of the trace stimulus whether or not responding occurred in the presence of the trace stimulus

Stimulus control of respondent and operant key pecking: A single key procedure

Pigeons' responses to a uniformly illuminated response key were either reinforced on a variable-interval one-minute schedule of reinforcement or extinguished for one-minute periods. When 1.5 second signals were presented at the beginning of each component, so as to differentially predict reinforcement, the pigeons pecked at the signals, at rates higher than rates during the remainder of the component. When the brief signals were not differentially predictive of reinforcement, pecking in their presence decreased to near zero levels. Similar results were obtained with signals based upon colors and upon line orientations. Changes in rates of (unreinforced) pecking occurred during the signal whether pigeons responded differentially during the remainder of the component or not. Experiment II demonstrated that the presence of the signal correlated with extinction was not necessary for pecking to develop at the signal which preceded the component in which responding was intermittently reinforced. The experiments demonstrated a clear dissociation of respondent control from operant control of a response. In addition, operant behavior was shown to be relatively insensitive to differing rates of reinforcement, as compared to the sensitivity of respondent behavior to differing rates of reinforcement produced by the very same operant behavior