The Effects of Hippocampal and Area Parahippocampalis Lesions in Pigeons: I. Delayed Matching to Sample

Four experiments were conducted to determine the effects of bilateral damage to the hippocampus and area parahippocampalis (Hp-APH) on visual memory in pigeons using the delayed matching-to-sample (DMS) procedure. In Experiment 1, we generated visual retention gradients with delays of 0, 1.5, 3, 6, and 12 sec both preoperatively and postoperatively in three pigeons with considerable preoperative visual DMS experience. Bilateral Hp-APH lesions had no effect whatsoever on visual retention. In Experiment 2, we examined the effects of Hp-APH lesions on both the acquisition of a visual DMS task with a 0-sec delay, and the subsequent retention performance with delays of 0, 3, 6, 12, and 24 sec. There was no difference between unoperated control pigeons and Hp-APH pigeons either in terms of the number of sessions required to learn the visual DMS task or in terms of their subsequent visual retention performance levels. In Experiments 3 and 4, we examined whether Hp-APH pigeons might be more sensitive than control pigeons to the effects of proactive interference (by reducing the duration of the intertrial interval) and retroactive interference (by introducing delay-interval illumination). Although reducing the duration of the intertrial interval and increasing the level of delay-interval illumination both resulted in lower performance levels on the visual DMS task, there was no indication that the Hp-APH pigeons were any more affected by the changes in interference levels than were unoperated control pigeons. These findings support the view that the Hp-APH in pigeons plays little role in the processing and retention of purely visual information.     

Matching-to-sample accuracy on fixed-ratio schedules.

Pigeons performing on a matching-to-sample procedure were exposed to six fixed-ratio (FR) schedules (FR 1, 5, 10, 20, 40, and 60) of food reinforcement for correct matching responses. During both a correction and a noncorrection procedure without an intertrial interval (ITI), matching accuracy was lower on FR 1 and FR 60 than at intermediate ratios. With the FR 1 schedule, both a 5-sec and a 25-sec ITI resulted in higher matching accuracy than without an ITI; accuracy, with an ITI, was fairly constant for ratios of 1 to 20 but declined at higher ratios. The results suggest that the presence or absence of an ITI in matching to sample may account for inconsistencies obtained in earlier studies of the relationship of matching accuracy to ratio size.     

The sex difference in rotary pursuit performance: aptitude or inhibition?

This study examined the hypothesis that male dominance in the acquisition and performance of rotary pursuit skill reflects a lower male proclivity for the generation and accumulation of reactive inhibition rather than some innately superior ability to profit from practice. On this hypothesis, the magnitude of male dominance should decline as the length of the intertrial interval increases. The experimental sample consisted of 120 Caucasian subjects (60 of each sex) who were given sixty 30-sec trials on rotary pursuit with intertrial intervals ranging from 0 to 40 sec. The principal finding was that the magnitude of the sex difference depended significantly upon the length of the intertrial interval, as hypothesized. When the interval was 10 sec or longer, performance levels of the sexes were essentially equal. The sex variance was reduced to insignificance even on the first trial when allowance was made for the inhibitory effect of practice. Thus, male dominance in rotary pursuit skill appears to be a procedural effect mediated by and inhibitory mechanism rather than a consequence of differential endowments of learning ability.     

The Sex Difference in Rotary Pursuit Performance

This study examined the hypothesis that male dominance in the acquisition and performance of rotary pursuit skill reflects a lower male proclivity for the generation and accumulation of reactive inhibition rather than some innately superior ability to profit from practice. On this hypothesis, the magnitude of male dominance should decline as the length of the intertrial interval increases. The experimental sample consisted of 120 Caucasian subjects (60 of each sex) who were given sixty 30-sec trials on rotary pursuit with intertrial intervals ranging from 0 to 40 sec. The principal finding was that the magnitude of the sex difference depended significantly upon the length of the intertrial interval, as hypothesized. When the interval was 10 sec or longer, performance levels of the sexes were essentially equal. The sex variance was reduced to insignificance even on the first trial when allowance was made for the inhibitory effect of practice. Thus, male dominance in rotary pursuit skill appears to be a procedural effect mediated by an inhibitory mechanism rather than a consequence of differential endowments of learning ability.     

Concept identification: Effect of the intertrial interval on the efficacy and consistency of information processing

Two experiments following identical procedure except for the feedback duration (respectively, 2 sec and 1.5 sec) and the intertrial interval (respectively, 1 sec and 3 sec) are compared with respect to three sequential statistics whose theoretical interpretation is related to the degree of optimality of information processing. The results indicate that the values of the theoretical parameters representing the efficiency of information processing, the consistency of trial-by-trial decisions, and the efficacy of reinforcement are greater in the 3-sec interval condition. This is interpreted as a tentative explanation of the well-known effect of intertrial interval on the difficulty of the task with respect to the mean number of trials to criterion.     

Optimal Stimulus Parameters In Avoidance Conditioning Of Inbred Strains Of Mice

Highly inbred mice of fast and slow conditioning strains (N = 228) were trained in avoidance conditioning and 180 were continued to extinction. The principal goal was to determine optimal stimulus conditions for fast learning, small variances, and maximal strain differences. Conclusions are: a) the major effect of change in CS-US and intertrial intervals occurs, respectively, for intervals less than 3 sec. and 60 sec.; b) change in amperage (150-400 pa) or voltage (250-400 v.) caused no significant differences; c) strain differences in extinction occurred after nearly optimal conditioning, and d) strain differences were altered considerably as stimulus conditions became optimal. Optimal levels of parameters are: 3 sec. CS-US interval, 120-sec. intertrial interval, and 400 v. (220 K ohm impedance circuit).     

Pigeons group time intervals according to their relative duration

In the present research, we asked whether pigeons tended to judge time intervals not only in terms of their absolute value but also relative to a duration from which they must be discriminated (i.e., longer or shorter). Pigeons were trained on two independent temporal discriminations. In one discrimination, sample durations of 2 and 8 sec were associated with, for example, red and green hue comparisons, respectively, and in the other discrimination, sample durations of 4 and 16 sec were associated with vertical and horizontal line comparisons, respectively. If pigeons are trained on a temporal discrimination and tested with intermediate durations, the subjective midpoint typically occurs close to the geometric mean of the two trained values. The 4- and 8-sec values were selected to be the geometric mean of the two values in the other discrimination. When a 4-sec test sample was presented with the comparisons from the 2- and 8-sec discrimination, the pigeons preferred the comparison associated with the shorter sample. Similarly, when an 8-sec test sample was presented with the comparisons from the 4-and 16-sec discrimination, the pigeons preferred the comparison associated with the longer sample. Thus, a relative grouping effect was found. That is, durations that should have produced indifferent choice were influenced by their relative durations (shorter than or longer than the alternative) during training.     

Trace autoshaping: Acquisition, maintenance, and path dependence at long trace intervals

The pigeon's tendency to acquire and maintain signal-directed key pecking under a trace conditioning procedure was parametrically examined. In Experiment 1, the percentage of CS trials with a key peck response was a decreasing function of the trace interval for separate groups of pigeons. The majority of subjects acquired signal-directed key pecking with trace intervals as long as 36 sec. In Experiment 2, differential maintenance of key pecking occurred across trace intervals in a within-subject procedure. Maintenance of key pecking at 36- and 60-sec trace intervals was path dependent in that responding depended on the subject's performance under the preceding trace interval.     

Temporal parameters of the feature positive effect

Trial duration and intertrial interval duration were parametrically varied between groups of pigeons exposed to a discrimination involving the presence vs. the absence of a dot. Half the groups received the dot as the positive stimulus (feature positive groups) and half the groups received the dot as the negative stimulus (feature negative groups). Faster learning by the feature positive birds (feature positive effect) was found when the trial duration was short (5 sec) regardless of whether the intertrial interval was short (5 sec) or long (30 sec). No evidence for a feature positive effect was found when the trial duration was long (30 sec) regardless of the length of the intertrial interval (30 sec or 180 sec). The results suggest that short trial duration is a necessary condition for the occurrence of the feature positive effect, and neither intertrial interval nor trial duration/intertrial interval ratio are important for its occurrence. The suggestion that mechanisms underlying the feature positive effect and autoshaping might be similar was not supported by the present experiment since the trial duration/intertrial interval ration parameter appears to play an important role in autoshaping but not the feature positive effect.     

Children's reactions to failure as a function of interresponse interval

Several studies have reported that nonreward facilitates subsequent performance; other studies have found that failure is followed by a performance decrement. Experiments that have shown facilitating effects of nonreward have used interresponse intervals of at least 5 sec, whereas those that have shown decremental effects of failure have used 0-sec interresponse intervals. The present study examined the effects of .5-, 1.0- and 5.0-sec interresponse intervals on children's lever-pulling responses following success and failure on a ball tower task. Second- and third-grade children responded slower following failure relative to success with .5- and 1.0-sec interresponse intervals. Speeds following success and failure did not differ when the interresponse interval was 5.0 sec. Increases in interresponse interval were associated with increases in speeds following failure, but speeds following success were not related to interresponse interval. These results were discussed in terms of frustration-produced competing responses and Elliott (1970) analysis of the influence of preparatory intervals on children's reaction-time performance.     

Preference for mixed versus constant delay of reinforcement

Preference for constant and mixed delay of reinforcement was studied using concurrent equal variable-interval schedules. For four pigeons, pecking one key was reinforced following constant delays of 8 sec and mixed delays of 6 or 10 and 2 or 14 sec. Pecking a second key was reinforced following constant delays of 0, 8, 16, and 32 sec. For two additional pigeons, pecking one key was reinforced following delays of 30, 15 or 45, 5 or 55, and 0 or 60 sec. Reinforcements on the other key were delayed 30 sec. It was found that (a) pigeons preferred mixed relative to constant delay of reinforcement, and (b) preference for mixed delay of reinforcement increased as the range of delay interval variability increased.     

Rate changes after unscheduled omission and presentation of reinforcement

Changes in response rate similar to frustration effects were studied in a two-lever situation. Responding on one lever on a fixed-interval schedule produced access to water for 5 sec and an exteroceptive stimulus. In the presence of this stimulus, responding on another lever on a fixed-interval schedule produced access to water for 5 sec and terminated the stimulus. Occasional omission of a previously scheduled reinforcer after responding on the first lever resulted consistently in increases in rate on the second lever during the immediately succeeding interval. In another procedure, occasional presentation of a previously unscheduled reinforcer after responding on the first lever resulted consistently in decreases in rate on the second lever during the immediately succeeding interval. Changes occurred after the first omissions or presentations and were about the same in magnitude as the procedure continued over several sessions. Typically, an increase or decrease in rate was maintained throughout an entire 100-sec interval. Changes in rate on the second lever of approximately the same magnitude also occurred when rate on the first lever was near-zero under a schedule that differentially reinforced behavior other than lever pressing.     

Delayed choice responding by pigeons when the correct response is not predictable from the sample stimulus.

Food-deprived pigeons were presented with a row of four response keys situated above a grain hopper aperture. At the start of a trial, three of four keys were randomly selected and illuminated white for six seconds. After a variable blackout period, one of the three previously white keys and the previously dark key were illuminated green, and the remaining white keys were reilluminated as before. A response to the green key that was previously white was reinforced with three-second access to gain, a response to any other key resulted in a three-second blackout and the start of a new trial. Five of six subjects responded to the correct green key more often than chance at an interstimulus interval of 1.5 seconds, and they displayed maximal performance at different intertrial interval values ranging from 15 to 60 seconds. Choice accuracy decreased for all but one subject as the interstimulus interval was increased. For the range of interstimulus interval durations employed, decrements in choice accuracy were qualitatively similar to, but lower than those typically obtained from, delayed-matching-to-sample or delayed-pair comparison procedures.     

Stimulus control of the pigeon's ability to peck a moving target.

Two pigeons were trained to peck whichever of eight keys displayed a white field (SD). The other seven keys displayed a white "X" on a black background (S delta). Each peck to SD produced three-second access to grain, a three-second intertrial interval (ITI), and the next trial. Pecks to S delta produced a three-second timeout (TO) and the same trial. During later sessions the key displaying SD changed every t seconds (t = 3, 2, 1, .5, and .25 sec), requiring the birds to track the position of the SD. Pecks on a ninth key increased t. Several sessions employed novel stimuli to ascertain the controlling stimulus dimensions. Both birds made few errors acquiring the original discrimination. During the tracking sessions, both birds made few errors when t = .5 sec. Only one reliably lengthened t. Data from sessions with novel stimuli indicate that color and form were important aspects of SD and S delta respectively; movement contributed to the final performance.     

The effects of temporal delay and orientation on haptic object recognition

We examined the effects of interstimulus interval (ISI) and orientation changes on the haptic recognition of novel objects, using a sequential shape-matching task. The stimuli consisted of 36 wedge-shaped plastic objects that varied along two shape dimensions (hole/bump and dip/ridge). Two objects were presented at either the same orientation or a different orientation, separated by either a short (3-sec) ISI or a long (15-sec) ISI. In separate conditions, ISI was blocked or randomly intermixed. Participants ignored orientation changes and matched on shape alone. Although performance was better in the mixed condition, there were no other differences between conditions. There was no decline in performance at the long ISI. There were similar, marginally significant benefits to same-orientation matching for short and long ISIs. The results suggest that the perceptual object representations activated from haptic inputs are both stable, being maintained for at least 15 sec, and orientation sensitive.     

Preference for fixed-interval schedules: effects of unequal initial links

Six homing pigeons were trained on concurrent chain schedules in which the terminal links were fixed-interval schedules of 5 sec or 15 sec. One initial-link schedule was always VI 27-sec; the other was varied over conditions from VI 27-sec to VI 181-sec. Preference measured in the initial links varied as a joint function of the initial- and terminal-link schedules. When the initial links were varied with constant, but unequal, terminal links, the slope of the function relating the logarithm of the initial-link response ratio to the logarithm of the terminal-link entry ratio differed from that obtained with equal terminal links. This result indicates that biases attributable to the terminal-link schedules were not constant. The rate of change of preference, or degree of undermatching, in the initial links depended on whether the shorter initial link led to the shorter or the longer terminal link. These results raise the question of whether bias and undermatching in concurrent schedule performance are independent measures.     

The effects of number of responses on the postreinforcement pause in fixed-interval schedules

The present study manipulated the number of responses in a modified fixed-interval schedule by imposing a blackout after each unreinforced response during the interval. The blackout duration was varied, and the duration of the fixed interval was held constant. The subjects were initially exposed to a fixed-interval 300-sec schedule. Blackout durations of 0, 10, and 50 sec were used. Following this, a fixed-interval 30-sec schedule was used with blackout durations of 0, 1, and 5 sec. Under the fixed-interval 300-sec schedule, the number of interreinforcement responses varied over a wider range than occurred under the fixed-interval 30-sec schedule. The duration of the postreinforcement pause decreased as blackout durations were increased and number of responses decreased on the fixed-interval 300-sec schedule, but pause length did not vary with changes in blackout duration and number of responses for the fixed-interval 30-sec schedule. The differences in the effects of blackout duration and response manipulation on the two fixed-interval schedules were attributed to relatively greater changes in the number of interreinforcement responses for the fixed-interval 300-sec schedule.     

Pavlovian conditioning of shock-elicited aggression: a discrimination procedure

Two auditory stimuli, separated by a fixed intertrial interval, were alternately presented to two rats in a closed environment. The positive conditioned stimulus (CS+) terminated with the offset of a 2-mA, 0.75-sec shock. The negative conditioned stimulus (CS-) terminated without shock. The incidence of the "stereotyped fighting posture" was recorded during the CS+, the CS-, the intertrial interval, and shock. The results showed an increase in the percentage of conditioned responses during the CS+, and a decrease during both the CS- and the intertrial interval, when the duration of the conditioned stimuli and the intertrial interval was 16 sec. Appropriate changes in the incidence of aggression during the two stimuli were obtained following the reversal of the stimulus functions. During the acquisition and reversal phases there was a between-session decrement and a within-session improvement in the incidence of aggression during the CS+, defined as warm-up. The presentation of free shocks before the conditioning sessions was effective in reducing the warm-up only when the interval between shocks was 64 sec. These data were interpreted as demonstrating classical conditioning of shock-elicited aggression, with little chance of non-associative factors contributing to the measurement of the conditioned response.     

The role of context in intertrial interval effects in autoshaping

Two experiments evaluated the role of differential conditioning of the context in mediating the effect of intertrial interval (ITI) in autoshaping. In Experiment 1 pigeons were given acquisition with two keylights, each presented in a particular context. A given keylight/context combination had associated with it either a short (10-sec) or a long (2-min) ITI. Acquisition was more rapid with the long ITI. Tests with those keylights in a common third context indicated that the longer ITI had resulted in greater conditioning. On the other hand, pigeons trained on keylights with mixed ITIs in a third context evoked more responding when they were tested in the short ITI context compared with the long ITI context. That suggests that a context with a history of a short ITI enhances performance. In Experiment 2, two keylights were initially conditioned with mixed ITIs and then extinguished in different contexts under different ITI lengths. Extinction was more rapid for the keylight presented with a short ITI. That difference persisted when the keylights were tested with mixed ITIs in a common third context, suggesting a difference in associative strength of the keylights. The results are interpreted in terms of differential context conditioning resulting in differences in learning about the keylight.     

The role of instrumental responding and contiguity of stimuli in the development of infant secondary reinforcement

Ten-month-old infants received contingent pairings of a tone (T+) and food reinforcer. Groups S^r and S^D received the food on an FI 23-sec schedule for target touching, the former group receiving T+ immediately after the response and 1.5 sec prior to food and the latter group receiving T+ at the end of the intertrial interval. Group SC received food reinforcers 1.5 sec after T+ with no response required. A second tone (Tⁿ) was heard by all groups once during each intertrial interval, at randomly determined points. All groups subsequently were given a spatial discrimination task, receiving T+ for one alternative and Tⁿ for the other. Group S^r gave significantly more responses for T+ than for Tⁿ, but neither of the other two groups produced a superiority for T+. Thus, both contiguity with a primary reinforcer and the presence of an operant during training appear to be necessary for a neutral signal to acquire the ability to enhance responding.