共查询到20条相似文献，搜索用时 78 毫秒
1.
Edward F. Meehan 《Learning & behavior》1979,7(4):473-476
Match-to-sample and oddity-from-sample problems with four colors were acquired by two pigeons under the supraordinate control of a line tilt superimposed on samples, Since the supraordinate stimulus terminated before the comparison stimuli were presented, accurate matching and oddity performance indicated trace stimulus control as well, The temporal extent of trace control was assessed in one subject by presenting probes—trials without a line tilt on the sample—in which the basis of correct responding was the supraordinate stimulus presented on the previous trial, Trace supraordinate control did not extend between trials, Subsequently, the delay between the termination of the supraordinate stimulus and the presentation of the comparison stimuli was gradually increased within a trial, Both subjects were able to perform matching and oddity over longer delays, and eventually on probe trials, although accuracy decreased, Results were discussed in terms of instructional stimulus control and memory. 相似文献
2.
Selective attention in processing of visual information by pigeons, trained on alternating sessions with two colors (red and
green) and two forms (a diamond and an X shape) differentially associated with a left—right key choice task, was examined.
A color and a form were presented together on probe trials during sessions in which, on other trials, only one of the dimensions,
color or form, was shown. The dimension in effect on the surrounding trials had no influence on choice when the information
provided by the two dimensions on probe trials was in conflict—color correct for one choice and form for the other. When both
color and form redundantly cued the correct choice, there was no increase in accuracy in comparison with that associated with
one dimension. Following separate training on the color and form discriminations, pigeons appeared to base their choices on
color on some trials, on form on other trials, but not on both simultaneously. These findings are discussed in terms of an
exemplar model of information processing. 相似文献
3.
Acquisition,extinction, and reacquisition of a conditional discrimination to avoid shock by goldfish
D. J. Zerbolio 《Learning & behavior》1984,12(2):163-170
Goldfish, trained in the shuttlebox to avoid shock, were tested for the acquisition and extinction of a color-matching or a color-oddity conditional discrimination choice response, and then tested for reacquisition. Extinction affected the accuracy of the choice response but not the number of trials with response (response strength). Half of all groups were extinguished with changed signal colors, and half had the same signal colors experienced in acquisition. All groups had the same signal colors in reacquisition that they had experienced in acquisition. Changed-signal oddity groups decremented slightly faster than same-signal oddity groups, providing some support for a generalization decrement interpretation, but same- and changed-signal matching groups did not differ. All groups extinguished on the choice response by the end of extinction. All matching groups, and all oddity groups, regardless of their respective signal colors in extinction, reacquired at the same rate, and faster than in acquisition. These results imply conceptual generalization of extinction effects. Matching-trained groups were found to be slightly superior to oddity-trained groups in both acquisition and reacquisition. Comparisons of these results to positive reinforcement conditional discrimination extinction work, including some procedural suggestions, are made. 相似文献
4.
Pigeons have difficulty learning a standard oddity task involving two colors and three stimulus positions. In Experiment 1, performance on standard noncorrection trials was compared with performance on (1) rerun correction trials in which errors resulted in trial repetition, (2) noncorrection trials with added “negative instance” trials involving presentation of three stimuli, all of which matched, and (3) a combination of correction and added negative instance trials. Results indicated that negative instances, but not correction trials, significantly facilitated oddity performance. In Experiment 2, Phase 1, number of stimulus positions lit (three or five) was factorially manipulated with number of positions on which the odd stimulus could appear (three or five). An increase in number of positions lit, but not number of positions that could be odd, facilitated performance. In Phase 2, birds transferred from trials with five positions lit to four positions lit performed significantly better than controls; but in Phase 3, the same birds did not perform significantly better than controls when transferred to trials with three positions lit. In both experiments, analysis of performance as a function of response position indicated better performance at the end of each display than in the middle. These results, together with the group performance differences in Experiment 2, suggest that oddity learning in pigeons involves a size, or number, discrimination. 相似文献
5.
An attempt was made to train 9 homing pigeons to respond to the presence or absence of bar magnets by turning either left or right after flying the length of a 20-ft outdoor flight cage. During initial training, color cues were placed in front of feeding stations on the left and right sides of the cage. The color cues were paired with magnetic cues by attaching either bar magnets or brass bars to the backs of the birds. The color cues were then deleted, leaving only the magnetic cues. Each pigeon received about 300 trials of color training followed by about 200 trials of magnet testing. When only magnetic cues remained, none of the pigeons were able to choose the correct feeder at greater than chance levels of probability. 相似文献
6.
Pigeons learned to respond at one spatial position when a pair of stimuli matched and at a different spatial position when they mismatched. All birds were then transferred to novel stimuli on an orthogonal dimension. For the positive-transfer group, the correct positions for matching and mismatching stimuli remained as they were during training. For the negative-transfer group, the correct positions were reversed. In Experiment 1, the birds were trained with shape stimuli and transferred to hue stimuli. Significant group differences were found, in spite of considerable stimulus-specific learning. In Experiment 2, when the same birds (counterbalanced for Experiment 1 transfer group) were transferred to steady-intermittent stimuli, even larger group differences were found. The data indicate that pigeons have some capacity for representing the concepts “same” and “different” with arbitrary stimuli (i.e., symbols). The data further suggest that distinctions that have been made between matching/oddity transfer tasks and same/different tasks may be procedural rather than conceptual. 相似文献
7.
Two pigeons were trained on a six-key modified oddity-from-sample procedure. The stimuli were olor pictures of birds, butterflies, and human faces. Initially, the third peck on the sample key which presented one of three different bird pictures) lit only one comparison key. Every three dditional pecks on the sample illuminated another comparison key. Fifteen sample pecks produced he maximum of five comparison stimuli. A peck on the comparison key that presented the non-atching bird picture produced grain. Pecks on matching keys turned off all the comparison keys nd repeated the trial. The birds learned to peck each sample until the non-matching comparison timulus was produced, and then to peck that key. After acquisition (70%–90% accuracy), the hree bird stimuli were replaced by a new set of three bird pictures. Subsequent phases provided ew sets of bird, butterfly, and human face stimuli. Both birds showed transfer of oddity learning o the novel samples. The data suggest that the birds may have been engaging in conceptual-type oddity learning, rather than learning discrete five-key discriminations or a series of two component chains. 相似文献
8.
We studied behavioral flexibility, or the ability to modify one’s behavior in accordance with the changing environment, in pigeons using a reversal-learning paradigm. In two experiments, each session consisted of a series of five-trial sequences involving a simple simultaneous color discrimination in which a reversal could occur during each sequence. The ideal strategy would be to start each sequence with a choice of S1 (the first correct stimulus) until it was no longer correct, and then to switch to S2 (the second correct stimulus), thus utilizing cues provided by local reinforcement (feedback from the preceding trial). In both experiments, subjects showed little evidence of using local reinforcement cues, but instead used the mean probabilities of reinforcement for S1 and S2 on each trial within each sequence. That is, subjects showed remarkably similar behavior, regardless of where (or, in Exp. 2, whether) a reversal occurred during a given sequence. Therefore, subjects appeared to be relatively insensitive to the consequences of responses (local feedback) and were not able to maximize reinforcement. The fact that pigeons did not use the more optimal feedback afforded by recent reinforcement contingencies to maximize their reinforcement has implications for their use of flexible response strategies under reversal-learning conditions. 相似文献
9.
There is evidence that humans' perception of time is affected by the activity in which they are engaged while they are timing. The more demanding the task, the faster time appears to pass. A similar effect has been found in pigeons. Pigeons trained to discriminate between a short-duration (2-sec) and a long-duration (10-sec) stimulus were required to peck when the stimulus was one color and to refrain from pecking when it was a different color. On probe trials of intermediate durations, the bisection point (50% choice of the stimulus associated with both long and short stimuli) for trials in which the pigeons were required to peck was almost 1 sec longer than on trials in which the pigeons were required to refrain from pecking (Zentall, Friedrich, & Clement, 2006). In the present research, we replicated this effect and determined the relation between this effect and the typical bisection point that occurs when pecking is permitted but not required. Results indicated that the typical procedure results in a bisection point that is between required pecking and refraining from pecking. Furthermore, the rate of pecking when pecking is allowed but not required also falls between the rate of pecking for the required-pecking and refrain-from-pecking conditions. This result suggests that, similar to humans, pigeons underestimate the passage of time when they are active or when attention to time-related cues has to be shared with attention to satisfying the response requirement. 相似文献
10.
Four experiments assessed the role of reinforcement expectancies in the trial spacing effect obtained in delayed matching-to-sample by pigeons. In Experiment 1, a differential outcome (DO) group received reinforcement with a probability of 1.0 for correct comparison responses following one sample stimulus and a probability of 0.2 for correct comparison responses following the other sample stimulus. The nondifferential outcome (NDO) group received reinforcement with a probability of 0.6 for correct responses to either stimulus. While matching accuracy was higher for the DO group than for the NDO group, both groups showed an equivalent decline in accuracy as the intertriai interval (ITI) duration was decreased. However, within the DO group, ITI duration affected performance on low-probability-of-reinforcement trials but not on high-probability-of-reinforcement trials. In Experiment 2, delay interval (DI) duration was 5, 10, or 15 sec and accuracy was higher for the DO group than for the NDO group at all DI durations. In addition, accuracy decreased similarly on high- and low-probability-of-reinforcement trials for the DO group as DI was increased. In Experiment 3, all birds were studied under DO conditions and ITI duration was manipulated along with DI duration. At the short DI duration, decreasing ITI duration had a detrimental effect on low-probability-of-reinforcement trials but no effect on high-probability-of-reinforcement trials. At the long DI duration, decreasing ITI duration had detrimental effects on both types of trials. In Experiment 4, unsignaled ITI reinforcers disrupted accuracy when the DI was long and when the ITI was short. The applicability of scalar expectancy theory to these data is discussed. 相似文献
11.
Adult pigeons with one eye covered were trained to peck a response key using grain as a reinforcer. In subsequent tests, with the trained eye covered and the control eye open, the birds failed to peck the key. The subjects were then divided into two groups for a second experiment. The first group was trained on a single-key, peck/no-peck color discrimination task with the original control eye covered. When tested for interocular transfer of discrimination performance, these birds failed to respond at all. They were then trained to peck a blank response key with the training eye covered and the control eye open. Control-eye tests after this motor response training resulted in excellent transfer of color discrimination performance. The second group of subjects was trained to peck a blank key with first one eye covered and then the other, before monocular discrimination training was begun. These birds showed excellent transfer of discrimination performance during control-eye tests. These results show that, at least in the operant paradigm, motor response training does not transfer interocularly and this lack of transfer may interfere with transfer of discrimination performance. 相似文献
12.
Kelly J. Stanhope 《Learning & behavior》1989,17(3):311-321
A dissociation between the effect of reinforcer type and response strength on the force of the pigeon’s keypeck response was shown in three experiments. In Experiment 1, pigeons were trained to peck two conditioned stimuli, one paired with water and another paired with grain. The pigeons made more forceful pecks for grain than for water and also showed a tendency, albeit an unreliable one, to respond on a higher percentage of food trials than water trials. In Experiment 2, the pigeons from Experiment 1 were satiated with either food or water and were then presented with the two conditioned stimuli in an extinction test. It was found that, regardless of the drive state, the pigeons made more forceful pecks to the stimulus that predicted food than to the stimulus that predicted water. In the thirsty group, however, this difference in force was not accompanied by a difference in the percentage of trials with a response. In Experiment 3, pigeons trained with a single reinforcer pecked more often on instrumentally reinforced trials than on Pavlovian conditioning trials, but there was no difference in the force of the pecks. Taken together, these results imply that differences in response strength cannot account for the difference between the force of food- and water-reinforced pecks. Instead, stimulus-substitution theory may provide the best account of the topography of the two types of pecks. 相似文献
13.
In Experiment 1, three food-deprived pigeons received trials that began with red or green illumination of the center pecking key. Two or four pecks on this sample key turned it off and initiated a 0- to 10-sec delay. Following the delay, the two outer comparison keys were illuminated, one with red and one with green light. In one condition, a single peck on either of these keys turned the other key off and produced either grain reinforcement (if the comparison that was pecked matched the preceding sample) or the intertrial interval (if it did not match). In other conditions, 3 or 15 additional pecks were required to produce reinforcement or the intertrial interval. The frequency of pecking the matching comparison stimulus (matching accuracy) decreased as the delay increased, increased as the sample ratio was increased, and decreased as the comparison ratio was increased. The results of Experiment 2 suggested that higher comparison ratios adversely affect matching accuracy primarily by delaying reinforcement for choosing the correct comparison. The results of Experiment 3, in which delay of reinforcement for choosing the matching comparison was manipulated, confirmed that delayed reinforcement decreases matching accuracy. 相似文献
14.
Douglas S. Grant 《Learning & behavior》1982,10(1):7-14
In two matching-to-sample experiments, pigeons’ performance with samples of stimuli (red and green), number of responses (1 and 20), and reinforcers (food and no food) was assessed. Samples of red, 20 responses, and food were associated with the red comparison stimulus, and samples of green, 1 response, and no food were associated with the green comparison stimulus. On interference trials, three sample types were presented on each trial, and two of the samples (congruent) were associated with the correct comparison and the third sample (incongruent), with the incorrect comparison. Performance on interference trials was compared with that on control trials in which either two (Experiment 1) or three (Experiment 2) congruent samples were presented. It was found that presentation of an incongruent sample reduced matching accuracy markedly, and about equally, whether samples were presented successively or in compound. Although the type of sample that was incongruent was without effect, matching accuracy declined strongly as the recency of the incongruent sample increased. Serial position of the incongruent sample also influenced the shape of the retention function on interference trials. Presentation of the incongruent sample either first or second resulted in accuracy decreasing across the retention interval, whereas presentation of the incongruent sample last in the input sequence resulted in increasing accuracy across the retention interval. The theoretical implications of the findings are considered. 相似文献
15.
In Experiment 1, pigeons were trained to discriminate short (2 sec) and long (8 sec) durations of tone by responding to red and green comparison stimuli. During delay testing, a systematic response bias to the comparison stimulus correct for the long duration occurred. Tests of responding without the tone reduced accuracy on long-sample trials but not on short-sample trials suggesting that the pigeons were attending to the tone and not simply timing the total trial duration. The pigeons were then trained to match short (2 sec) and long (8 sec) durations of light to blue/yellow comparisons. During delay testing, “choose-long errors” occurred following tone durations, but “choose-short errors” occurred following light durations. In Experiment 2, accuracy was assessed on test trials in which the tone and the light signals were simultaneously presented for the same duration or for different durations. Pigeons responded accurately to durations of light, but were unable to accurately respond to durations of tone simultaneously presented with the light. The data from Experiment 1 suggest that there are important differences between light and tone signals with respect to the events that control the termination of timing. The data from Experiment 2 indicate that pigeons cannot simultaneously time visual and auditory signals independently and without interference. Consequently, they are inconsistent with the idea that there is a single internal clock that times both tone and light durations. 相似文献
16.
Pigeons were trained to learn an instrumental oddity-from-sample discrimination involving visual forms. One group, the “few examples” group, dealt with 5 patterns in 40 different combinations. Another group, the “many examples” group, dealt with 20 patterns in 160 different combinations. After both groups had reached asymptotic performance and had learned to operate under partial reinforcement conditions, they were tested for transfer under extinction conditions with two different groups of 5 novel patterns, each in 40 combinations. All animals showed significant above chance transfer to both of these novel stimulus sets. Transfer performance with test stimuli of similar geometric design to training stimuli was better than performance with stimuli of markedly different design. The transfer performance of the “many examples” group was marginally better than that of the “few examples” group, even though the latter’s performance on the training stimuli was better throughout. It is concluded that pigeons can learn to employ an oddity concept and that this may be promoted by the use of many training exemplars. Furthermore, it is inferred that pigeons may normally use a mixture of strategies to solve oddity and identity problems. 相似文献
17.
In matching-to-sample, comparison choice should be controlled by the identity of the sample and, when the sample is not available,
by the overall probability of reinforcement associated with each of the comparisons. In the present research, pigeons were
trained to match a frequent sample (appearing on 80% of the trials) to one comparison (C
fr) and an infrequent sample (appearing on 20% of the trials) to the other (C
inf), with the number of reinforcements associated with each sample equated. In Experiment 1, the task was identity matching;
in Experiments 2 and 3, it was symbolic matching. We asked whether, when control of comparison choice by the sample was reduced
(by inserting a delay between the sample and the comparisons), pigeons would choose comparisons on the basis of (1) the number
of reinforcements per comparison (and thus show no comparison bias), (2) the comparison associated with the more frequent
sample during training (and show a preference forC
fr), or (3) the probability of reinforcement given a correct response (and show a preference forC
inf), or (4) inhibition produced by nonreinforced choice of the more frequently correct comparison (and show a preference forC
inf). Pigeons showed a significant tendency to chooseC
fr. In Experiment 3, we showed that this bias did not result from the effects of intertrial facilitation or interference. Thus,
it appears that when control of comparison choice by the sample is reduced, pigeons’ choice is controlled not merely by the
probability of reinforcement but also by overall sample frequency. 相似文献
18.
Goldfish, trained in the avoidance shuttlebox with a variant of the linear discrimination procedure, learned to conditionally discriminate between color signals, both for the matching (M) and oddity (O) criterion forms. Transfer to assess the possibility of concept learning was also tested. In original learning, oddity-trained groups learned faster and reached higher conditional discrimination performance levels than did matching-trained groups. In transfer, various groups were tested with the same criterion (MM or OO) or a shifted criterion (MO or OM), and half of each group retained the same color signals and the remaining half had its color signals changed in transfer. Groups with the same criterion in original learning and transfer (MM or OO), regardless of signal colors, showed comparable positive transfer. Groups with their criterion shifted between original learning and transfer (MO or OM) showed comparable negative transfer, regardless of signal colors. Since both positive- and negative-transfer effects were independent of signal colors, it is clear that what was learned for one set of signal colors transferred to at least one other signal-color set. These findings are consistent with the interpretation that goldfish learned the original conditional discrimination at a conceptual level, and learned about the general matching or oddity relationships between colors, rather than about a specific set of colors. 相似文献
19.
Donald M. Wilkie 《Learning & behavior》1986,14(3):257-266
In the delayed matching of key location procedure, pigeons must remember the location of the sample key in order to choose correctly between two comparison keys. The deleterious effect of short intertrial intervals on key location matching found in previous studies suggested that pigeons’ short-term spatial memory is affected by proactive interference. However, because a reward expectancy mechanism may account for the intertriai interval effect, additional research aimed at demonstrating proactive interference was warranted. In Experiment 1, matching accuracy did not decline from early to late trials within a session, a finding inconsistent with a proactive interference effect. In Experiment 2, evidence suggestive of proactive interference was found: Matching was more accurate when the locations that served as distractors and as samples were chosen from different sets. However, this effect could have been due to differences in task difficulty, and the results of the two subsequent experiments provided no evidence of proactive interference. In Experiment 3, the distractor on Trialn was either the location that had served as the sample on Trialn ? 1 or one that had been a sample on earlier trials. Matching accuracy was not inferior on the former type of trial. In Experiment 4, the stimuli that served as samples and distractors were taken from sets containing 2, 3, 5, or 9 locations. Matching accuracy was no worse, actually slightly better, with smaller memory set sizes. Overall, these findings suggested that pigeons’ memory for spatial location may be immune to proactive interference. However, when, in Experiment 5, an intratrial manipulation was used, clear evidence of proactive interference was found: Matching accuracy was considerably lower when the sample was preceded by the distractor for that trial than when it was preceded by the sample or by nothing. Possible reasons why interference was produced by intratrial but not intertrial manipulations are discussed, as are implications of these data for models of pigeons’ short-term spatial memory. 相似文献
20.
When Pavlovian stimuli activate representations of food, do these representations resemble memories of food consumed in the recent past or expectancies of food that is imminent? In Experiments 1A and 1B, this question was addressed by training pigeons on a symbolic matching-to-sample task involving different grains as memory cues or as expectancy cues for correct choices. Autoshaping trials involving these same grains were interspersed among matching-to-sample trials, as were test trials involving the substitution of autoshaping stimuli for cues in the matching-to-sample task. Control over choices transferred to autoshaping stimuli in both experiments, suggesting that associatively activated representations of food resemble both memories and expectancies. In Experiment 2, pigeons were trained on a symbolic matching-to-sample task in which food and no-food memory cues (i.e., the samples) were juxtaposed with no-food and food expectancy cues. Subsequently, autoshaping stimuli, which activated representations of food and no food, were substituted for the samples. Choices by the pigeons indicated that associatively activated representations of food-related events resemble expectancies more closely than they do memories. 相似文献