Topography of spatially directed conditioned responding: effects of context and trial duration

Domesticated quail (Coturnix japonica) received a discrete conditioned stimulus (CS) at one end of the experimental chamber paired with the opportunity to copulate with a female quail (the unconditioned stimulus) in a goal box located 112 cm away. Approach to the CS (sign tracking) and approach to the goal area (goal tracking) were measured. The duration of exposure to the experimental context (C) was varied in Experiment 1, and the duration of the conditioning trials (T) was varied in Experiment 2 for independent groups, creating C/T ratios of 1.0, 1.5, 4.5, 45, and 180. Contrary to previous reports of a direct relation between the C/T ratio and conditioned responding, in the present experiments, a shift in the topography and stimulus control of conditioned behavior occurred. Low C/T ratios (1.0-4.5) produced goal tracking controlled by contextual cues, whereas high C/T ratios (45 and 180) produced sign tracking controlled by the discrete CS.     

Transfer of conditioned fear and avoidance: Concurrent measurement of arousal and operant responding

A reversal design was employed for the analysis of transfer of fear and avoidance through equivalence classes. Two 5-member equivalence classes (A1-B1-C1-D1-E1 and A2-B2-C2-D2-E2) were established. Then B1 and C1 were paired with shock (CS+) and served as S^Ds in avoidance training (B2 and C2 were trained as CS-/S^∆s for avoidance). Further avoidance training followed with D1 and E1 (as S^Ds) and D2 and E2 (as S^∆s), with the first presentation of each of these stimuli serving as the first transfer test. Afterwards, aversive conditioning contingencies were reversed: B2 and D2 were paired with shock and trained as S^Ds for avoidance, B1 and D1 were presented without shock (CS-/S^∆s). Transfer was tested again with C1, E1, C2 and E2. This reversal was implemented to allow for the within-subject replication of transfer effects upon changes in the function of only a subset of each class's elements. Avoidance (key presses) and conditioned fear (skin conductance and heart rate) were simultaneously measured. Results show a clear transfer effect for avoidance, with between- and within-subject replications. For physiological measures, transfer effects in the first test could only be imputed on the basis of group-based inferential statistical analysis. Evidence for between-subject replication was weaker, with only a limited proportion of participants meeting the individual criterion for transfer.     

The effects of aversive conditioned stimuli on the timing of unsignalled avoidance responding in rats

Rats received unsignalled avoidance training in a shuttlebox. After acquisition, classical conditioning sessions were administered. The Excitatory Group received signals paired with shock, the Inhibitory Group received signals explicitly unpaired with shock, while the Random Control Group received signals and shocks randomly in time. When subsequently superimposed on the avoidance baseline, the excitatory signal increased response rate, the inhibitory signal decreased rate and the random signal had no effect compared to signal-only control data. Unsignalled avoidance generates temporal gradients of responding; the major purpose of this study was to determine how these rate changes were reflected in the baseline temporal behavior. Very clear and simple summation rules emerged: In the presence of the excitatory signal, rats acted as if they were ahead of their actual location in the response-shock interval regardless of where the signal occurred; the inhibitory signal had the opposite effect while the random signal did not change the temporal behavior relative to signal-only control data. These results were interpreted within a motivational framework.     

Naloxone decreases responding for conditioned reinforcement in rats

That opioids can mediate unconditioned reinforcement is well established, but there is little evidence indicating whether they modify conditioned reinforcement. Here, a tone which initially served as a discriminative stimulus for the availability of water reinforcement was established as a conditioned stimulus. When later given a choice between pressing a lever producing the tone (but not water) or one which produced no effect, rats chose the tone-producing lever 66% of the time. Naloxone (3.0 mg/kg) reduced overall responding and completely eliminated the preference for the tone-producing lever. Results are briefly discussed in terms of the importance of understanding mechanisms serving conditioned reinforcement.     

Reduction of shock duration as negative reinforcement in free-operant avoidance

Rats were trained on a free-operant procedure in which shock duration was controlled by responses within a limited range of interresponse times. Shocks of 1.6-mA intensity occurred randomly with average density of 10 shocks per minute. As long as interresponse times were 15 seconds or less, any shocks received were at the briefer of two durations (.3 second). Whenever interresponse times exceeded 15 seconds, any shocks received were at the longer duration (1.0 second). For six of eight animals, avoidance responding developed quickly and reached levels of better than 90%. Four yoked animals stopped responding within the first few sessions. Shock duration reduction without change in shock probability or intensity was sufficient for the acquisition and maintenance of avoidance responding.     

Temporal control of conditioned responding in goldfish

The peak procedure was used to characterize response timing during acquisition and maintenance of conditioned responding in goldfish. Subjects received light-shock pairings with a 5- or 15-s interstimulus interval. On interspersed peak trials, the conditioned stimulus light was presented for 45 s and no shock was delivered. Peaks in the conditioned response, general activity, occurred at about the time of the expected unconditioned stimulus, and variability in the activity distribution was scalar. Modeling of the changes in the activity distributions over sessions revealed that the temporal features of the conditioned response changed very little during acquisition. The data suggest that times are learned early in training, and, contrary to I. P. Pavlov's (1927/1960) concept of "inhibition of delay," that timing is learning when to respond rather than learning when not to respond.     

The effect of rate of delivery of response-independent shocks upon avoidance responding

Two hooded rats were trained to bar-press to avoid electric shock on a continuous avoidance schedule with response-shock and shock-shock intervals equal. The rate of delivery of response-independent shocks superimposed on this schedule was varied. The response-independent shocks led to generally higher response rates but, with responses during shock omitted, the rates decreased as the response-independent shock rate was increased. The actual shock rate received by the subjects was linearly related to the maximum potential shock rate. There was an increasing, negatively accelerated function between percentage avoidance and response rate, but there was no consistent relation between the number of shocks avoided and response rate. Response rate decreased as the potential shock rate increased, but responding was maintained even when as few as 15% of the shocks could be avoided.     

Varying wheel-running reinforcer duration within a session: effect on the revolution-postreinforcement pause relation

Previous investigations of wheel-running reinforcement that manipulated reinforcer duration across conditions showed a strong relation between wheel-running rate and average postreinforcement pause (PRP) duration. To determine if the basis of this relation across conditions was a local effect of fatigue or satiation, the correlation between revolutions run and the duration of the immediately following PRP was investigated under conditions in which reinforcer duration was either constant or variable within a session. Seven male Wistar rats pressed a lever on a fixed-interval 60-s reinforcement schedule with the opportunity to run for 60 s as the reinforcing consequence. In the constant-duration condition, the duration of the reinforcer was always 60 s. In the variable-duration condition, the duration of the reinforcer varied between 2 and 240 s with a mean of 60 s. Mean correlations between revolutions run and the next PRP duration for constant, variable, and constant conditions were -.07, .20, and -.07, respectively. Although the positive correlation in the variable-duration condition is consistent with an effect of momentary fatigue or satiation, little of the variance in PRP duration appears to be attributable to these factors.