共查询到20条相似文献，搜索用时 31 毫秒
1.
Peter E. Jenkins 《Learning & behavior》1981,9(4):501-507
In Experiment 1, pigeons were exposed to a discriminative autoshaping procedure in which one keylight was correlated with negative automaintenance and the other keylight was correlated with positive automaintenance. The negative automaintenance procedure maintained shorter keypeck durations than the positive automaintenance procedure. Keypecking tended to occur in bursts of two, three, or four pecks, and within these bursts keypeck durations reliably decreased. In Experiment 2, keypeck durations and off-keypecks were initially examined during exposure to a positive automaintenance procedure. When a negative keypeck-reinforcer contingency was introduced, keypeck durations decreased and the ratio of off-keypecks to on-keypecks increased. When a positive keypeck-reinforcer contingency was introduced, keypeck durations increased and the ratio of off-keypecks to on-keypecks decreased. These results suggest that keypeck duration is determined by the extent to which the peck is directed at the key. 相似文献
2.
In Experiment 1, the development of autoshaped pecking to a keylight signaling food was blocked if the keylight was presented only in conjunction with another stimulus already established as a signal for food, even though the blocking stimulus (either an overhead light or a train of clicks) never elicited pecking itself. In Experiment 2, pigeons came to peck a white keylight which signaled the presentation of a red keylight which had earlier been established as a first-order signal for food, but this second-order autoshaping was blocked if the white keylight was presented only in conjunction with the houselight or clicker which had previously signaled the presentation of the first-order stimulus. Second-order autoshaping was thus blocked in the same way as was first-order autoshaping. 相似文献
3.
Eliot Hearst 《Learning & behavior》1989,17(3):280-290
During training intended to establish positive and negative backward associations, pigeons received periodic 3-sec illuminations of a grain magazine, with food simultaneously available on 50% of the illuminations. For backward-positive subjects, a red keylight followed food trials only; for backward-negative subjects, it followed no-food trials only. During this training, the birds hardly ever pecked the red stimulus (no evidence of backward conditioning). However, when the red stimulus subsequently preceded and signaled grain for all birds, the backward-positive subjects pecked sooner and more often than did the backward-negative subjects, and control subjects performed at an intermediate level. Increases in the amount of original training did not significantly change the facilitatory effects of the backward-positive stimulus, but seemed to enhance the retarding effects of the backward-negative stimulus. These group differences cannot be attributed to what happened after the backward stimuli during original training. The features of the present technique that could possibly have produced strong and long-lasting positive and negative backward associations are discussed in comparison to prior research that has indicated weak or transitory evidence of true backward conditioning. 相似文献
4.
Suzette L. Astley 《Learning & behavior》1987,15(4):368-374
The present experiment is concerned with the nature of the cues that might acquire conditioned reinforcing value, and the ways in which such cues might interact with one another. Red and green colored keylights were differentially paired with food dependent upon the houselight context (A or B) and the trial type (training or choice/forced). The duration of the colored keylights was varied between groups in an attempt to manipulate the effectiveness of the short-term memory of trial-type cues at the trial’s end. The red and green stimuli were of 30 sec duration for Group 30 and of 3 sec duration for Group 3. The results indicated that the choices of the pigeons in Group 30 were influenced by the houselight context present and by the keylight color. The choices of the pigeons in Group 3 seemed to be influenced by the houselight context present, the keylight color, and the memory of trial-type cues. Memory cues for trial antecedents were not overshadowed by presumably more salient external houselight stimuli for the pigeons in Group 3. Two alternative explanations for the results are discussed, and determined to be unlikely based on the results of an earlier experiment. The present results are related to a model of the conditioned reinforcing value of momentary stimuli and of transmission of conditioned reinforcing value. 相似文献
5.
In Experiment 1, two groups of pigeons were autoshaped to a green keylight CS and then administered either CS only or truly random control (TRC) response-elimination procedures with the green keylight CS. The groups ceased responding at comparable rates. In a subsequent reacquisition test with a vertical-line key stimulus, the group administered CS only during response elimination reacquired the keypecking CR more rapidly. The two groups were then administered the alternative response-elimination treatment with the vertical-line CS. Again, the groups ceased responding at comparable rates. In a subsequent reacquisition test with a red keylight CS, the group administered CS only during the immediately preceding response-elimination phase reacquired the keypecking CR more rapidly. In Experiment 2, following initial acquisition, the CS-only and TRC response-elimination treatments were administered under the context-change and no-context change conditions. The TRC/context-change and CS-only/context-change groups ceased responding more rapidly than either the TRC/ no-context-change or CS-only/no-context-change groups. In subsequent reacquisition to a novel CS, the CS-only/no-context-change group reacquired the fastest, the TRC/no-context-change group reacquired the slowest, and the CS-only/context-change and TRC/context-change groups reacquired at similar intermediate rates. Implications of these results for the context-blocking hypothesis are discussed. 相似文献
6.
In Experiment 1, two groups of pigeons (n = 8) were given nondifferential (ND) training with a green keylight and a white vertical line on a dark surround nonsystematically alternated. Two groups (n = 8) received single stimulus (SS) training with the green light only. In Experiment 2, two groups of pigeons (n = 8) were given ND training with vertical and horizontal lines, while two other groups (n = 8) received SS training with only the vertical line. In both experiments, all groups were transferred to a green S+ (VI reinforced) and a red S? (extinguished) transfer problem. In each experiment, one ND and one SS group was tested in the same context as initial training (houselight off) and one ND and one SS group was tested in a changed context (houselight on). In both experiments and in both contexts, the ND groups performed less well on the transfer problem than did the SS groups. There was no evidence of greater control by the context in ND than in SS groups, which suggests that the observed difference in acquisition of the transfer task is not attributable to a purported difference in control by the context under the two conditions. The overall results favor the position that nondifferential training reduces attention to stimuli involved in the original training procedure and that this reduced attention transfers to stimuli subsequently experienced. 相似文献
7.
Autoshaping procedures with pigeons were used to assess the susceptibility of unconditioned response (UR) activity to Pavlovian relations between stimulus and reinforcer events. Foodpeck latency (a measure of UR activity) was investigated as a function of the interval between stimulus (keylight) and reinforcer (grain) presentations, and of the stimulus-reinforcer contingency, that is, the conditional probabilities of reinforcer delivery in the presence and absence of the stimulus. Four experiments indicated that food-peck latency was sensitive to both manipulations. Generally, conditions that led to higher keypeck rates were associated with shorter latencies. Thus, UR potentiation was demonstrated. However, when the bird’s location prior to grain delivery was fixed by imposing a keypeck-reinforcer contingency, UR potentiation vanished; it then reappeared when the location constraint was removed. Visual observations supported the conclusion that food-peck latency effects were mediated by approach/withdrawal tendencies generated by the stimulus-reinforcer relation. Implications of these results for expectancy theory are discussed. 相似文献
8.
Edson M. Huziwara Saulo M. Velasco Gerson Y. Tomanari Deisy G. de Souza Armando D. Machado 《Learning & behavior》2013,41(2):192-204
In two experiments, we investigated emergent conditional relations in pigeons using a symbolic matching-to-sample task with temporal stimuli as the samples and hues as the comparisons. Both experiments comprised three phases. In Phase I, pigeons learned to choose a red keylight (R) but not a green keylight (G) after a 1-s signal. They also learned to choose G but not R after a 4-s signal. In Phase II, correct responding consisted of choosing a blue keylight (B) after a 4-s signal and a yellow keylight (Y) after a 16-s signal. Comparisons G and B were both related to the same 4-s sample, whereas comparisons R and Y had no common sample. In Phase III, R and G were presented as samples, and B and Y were presented as the comparisons. The choice of B was correct following G, and the choice of Y was correct following R. If a relation between comparisons that shared a common sample were to emerge, then responding to B given G would be more likely than responding to Y given R. The results were generally consistent with this prediction, suggesting, for the first time in pigeons, the emergence of novel relations that involve temporal stimuli as nodal samples. 相似文献
9.
Ken Cheng 《Learning & behavior》1992,20(2):112-120
The peak procedure was used in two experiments. Pigeons in the penalty group in Experiment 1 were rewarded with food in the first phase for the first peck after 12.5 sec had elapsed since the onset of a keylight. In the second phase, reward was withheld if the pigeons pecked within 6.25 sec after keylight onset. Responses in time were tabulated on occasional unrewarded tests in which the keylight was left on for 37.5 sec. Under the penalty contingencies, the response distribution in time remained nearly symmetric about the peak, while the spread of the distribution narrowed, and the time of peak responding came slightly earlier. The yoke group underwent a schedule of rewards similar to that for the penalty group, but without the penalty contingencies. Their response distributions remained similar throughout. The results of Experiment 1 were replicated in Experiment 2, which showed further that the changes due to the penalty contingencies did not generalize to the use of another key on which the penalty contingencies were not in effect. The narrower spread under the penalty contingencies is explained in terms of a change in threshold for when to start responding, and more weight being given to timing versus responding in the presence of the signal per se. No explanation was found for the change in the time of peak responding. 相似文献
10.
Five groups of pigeons were trained in a symbolic choice-matching feast involving short (2-sec) and long (10-sec) durations of houselight as samples. Four groups also received training with a second set of samples: line orientations or 2- and 10-sec presentations of keylight. The type of sample-to-comparison mapping varied across groups. Although only two of the five groups demonstrated a choose-short effect (a tendency to choose the comparison associated with a short sample at longer delays), all groups demonstrated temporal summation (a tendency to respond on the basis of the combined duration of two successively presented samples). Moreover, the magnitude of temporal summation was equivalent in groups that did and did not-demonstrate a choose-short effect. The results suggest that the processes underlying the perception of sample duration remain invariant across different sample-to-comparison mapping arrangements, but that the memory code used to retain temporal information varies. 相似文献
11.
Pigeon subjects received Pavlovian conditioning with stimulus elements and were then tested with compounds of those elements. Experiments 1–3 used localized keylight elements and found no evidence for greater responding to the compound than to the elements. Experiments 4A–4D found evidence for greater second-order conditioning by a compound of two elements than by the elements themselves when the elements consisted of two diffuse stimuli or one diffuse stimulus and one localized keylight. No greater second-order conditioning resulted from a compound of two localized keylight elements, suggesting the possibility of perceptual interactions that reduce identification of the elements in the compound. Experiment 6 found evidence of summation when that interaction was reduced by sequential presentation. However, one attempt to capture this interaction in terms of configural conditioning (Pearce, 1987) failed to receive confirmation. These results suggest that the localized stimuli conventionally employed in autoshaping experiments may show such substantial perceptual interaction as to recommend against their routine use for studying conditioning in compounds. 相似文献
12.
A second-order autoshaping procedure was used to examine the effects of three variables on the amount of information that could be learned about the stimulus properties of a reinforcer. All three experiments paired several keylight S2s with different keylight S1s and then carried out discriminative autoshaping with those S1s. Learning about the stimulus properties of S1 was inferred from changes in the response to its paired S2 when that S1 was changed in value. The sensitivity of S2 to changes in S1 was investigated as a function of number of S2-S1 pairings (Experiment 1), partial reinforcement (Experiment 2), and temporal distance between S2 and S1 (Experiment 3). Each experiment found evidence of a selective change in responding to an S2 as a function of the treatment of its S1. However, the amount of that change was not affected by any of the three variables studied. Those results imply that, within the ranges used here, none of these variables changes the degree of learning about the stimulus properties of a reinforcer. 相似文献
13.
Pigeons learned to peck a keylight (S2) when it was paired with a stimulus (S1) that already evoked keypecking. Control procedures showed that S2 acquired control over responding because it was paired with S1 and because S1 had a conditioning history, thereby supporting the claim that S2 was a second-order conditioned stimulus. Second-order conditioning occurred as rapidly when S1 was a keylight as when it was a tone. Test procedures showed that after second-order conditioning, responding to S2 was markedly debilitated by the extinction of responding to S1, indicating that the ability of S2 to evoke a response importantly depends upon the continued ability of S1 to do so. Our demonstration that directed motor action in the pigeon is susceptible to second-order conditioning suggests a new interpretation of conditioned reinforcement in instrumental learning. Our demonstration that the effectiveness of S2 depends upon the continued effectiveness of S1 indicates that S-S associations are formed in this version of the second-order conditioning experiment. 相似文献
14.
In three experiments, we sought evidence for the acquired equivalence of cues in pigeons trained in an autoshaping paradigm. In Experiment 1, presentations of each of a pair of cues (different keylight stimuli) preceded a common consequence (a different keylight stimulus). The pattern of response then established by further training given to one member of the pair was found to generalize preferentially to the other, demonstrating equivalence between cues that had shared a common consequence. The same test procedure was used in Experiment 2, but with a training procedure in which each cue of a pair was preceded by a given stimulus. This too resulted in enhanced generalization between members of the pair, showing that equivalence can be established when cues have been experienced along with a common antecedent. Both training procedures were combined in Experiment 3 to confirm the reliability of the effects previously obtained. The discussion is focused on ways in which the associative explanation offered for cases of equivalence mediated by a common consequence might be extended to accommodate equivalence mediated by a common antecedent. 相似文献
15.
Pigeons were given successive discrimination training in which pecking during a choice period when the key was white was either reinforced or not, depending upon the prior presence or absence of a discriminative stimulus, which was a two-element serial compound. The compound consisted of a keylight and food, with food presented second or first in a forward or backward pairing for different groups of pigeons. In Experiment 1, the sequence was an S+ indicating reinforced trials, while in Experiment 2, the sequence was an S? indicating nonreinforced trials. Following acquisition of discriminated operant behavior, a sequence generalization test was administered during which all possible orders of the two stimuli were presented on test trials prior to the onset of the choice period. The results showed that food overshadowed stimulus control by the color of the light on the key on the sequence-generalization test, independently of whether food was presented first or second during training and independently of whether food was associated with reinforcement or nonreinforcement. The similarity of results for the two experiments suggests that overshadowing occurs independently of whether the compound is a discriminative stimulus for reinforcement or nonreinforcement. Simultaneous presentation of elements of a compound stimulus is not necessary for overshadowing because the phenomenon was captured with sequentially presented stimuli. 相似文献
16.
Douglas S. Grant 《Learning & behavior》2001,29(4):293-301
Pigeons were trained to discriminate short (2 sec) and long (8 sec) empty intervals that began each trial. In group consistent,
onset of an empty interval was marked by a brief presentation of red keylight, and termination of the interval was marked
by a brief presentation of green keylight. In group inconsistent, red and green served equally often as the first and second
markers across trials. Testing revealed that, in group consistent, (1) birds were sensitive to the relation between marker
color and marker type and (2) presentation of the second marker did not initiate timing a new interval. Testing also revealed
a robust choose-long effect at delays longer than the training delay and indifference between the comparisons on no-sample
trials. Both of the latter findings differ from those typically obtained when filled intervals are employed. It was concluded
that pigeons process filled and empty intervals differently. 相似文献
17.
Robert A. Rescorla 《Learning & behavior》1991,19(1):65-70
An autoshaping paradigm with pigeon subjects was used to study two-types-of modulation: facilitation and inhibition. In each paradigm, a diffuse stimulus signaled when a keylight would be reinforced. Transfer of that diffuse stimulus to a different keylight was assessed after the response-evoking power of the original keylight had been altered in the presence of a different modulator. That alteration of the original target produced a specific change in the transfer of modulators trained with that target. The results are interpreted as suggesting that transfer to another target stimulus is partly mediated by the association of the original target with the reinforcer. They are inconsistent with at least one version of a configurai cue interpretation. 相似文献
18.
Pigeons were trained on a variant of the autoshaping procedure in which a keylight stimulus of increasing brightness was used to signal the passing of a 30-sec interfood interval (IFI). Key-pecking developed in all subjects within the first session (65 trials). Within trials, pecking began midway through the IFI, increased throughout the remainder, and decreased just before food delivery. Other behavioral stereotypies were also recorded: Low light levels were associated with a retreat to the rear of the test chamber, and medium light levels (during the midportion of the IFI) were associated with high rates of pacing toward and away from the food source. Probe trials revealed that pecking, pacing, and retreat were all under strong stimulus control; that is, when the light was held constant at its lowest or highest brightness, or when the brightness ramp was presented in reverse order, the behavior pattern almost invariably remained tied to stimulus brightness. Results are discussed in terms of associative and nonassociative sources of the form and sequential characteristics of the behavior. 相似文献
19.
In Experiment 1, six groups of pigeons (n=8) were tested for wavelength generalization either immediately or 24 h after learning a successive discrimination, with 550 nm reinforced and a black vertical line extinguished. The groups differed in the stimulus present during single stimulus pretraining, which was 550 nm (pretrain S+), the vertical Une (pretrain S?), or a neutral dim white light (pretrain Sn), respectively. The three immediate generalization gradients were steep and indistinguishable, reflecting only the immediately preceding discrimination training condition. The three delay gradients were flatter, with the flattening particularly marked in the pretrain S? group. This was interpreted as proactive interference (PI) resulting from the memory that both the 550-nm and the line stimuli had previously been reinforced. In Experiment 2, two (TD) groups of pigeons (n=16) were given single stimulus training with a 555-nm keylight followed by eight sessions of discrimination training with two line angles, then one session of non-differential (ND) training with the same two lines, and then a wavelength generalization test either immediately or after a 24-h delay. Two other (hold) groups (n=16) received similar training, except for the TD Une angle training sessions, in these hold groups, the wavelength gradient was flatter in a delayed test; in the TD groups it was steeper, indicating PI from the prior TD training. These two experiments suggest that the “attentional sets,” which purportedly result from TD and ND training, may fruitfully be viewed as target memories subject to the principles of interference theory. 相似文献
20.
Terry and Wagner (1975) have suggested that short-term retention of information about an event is enhanced if the occurrence of the event is surprising. To investigate this idea, we trained two groups of pigeons in a preparatory-releaser procedure in which half the trials started with the presentation of food (the preparatory event). The preparatory food presensation was signaled by an 8-sec white keylight in the signaled, but not in the unsignaled, group. After a retention interval, varying between 2 and 32 sec, the releaser stimulus (CSR), a red keylight, was presented for 8 sec in the absence of any reinforcement. The remaining trials were initiated by the presentation of CSR, and the first peck occurring 8 sec after the onset of CSR was reinforced by food. The preparatory event controlled responding to CSR at the short retention interval, with the level of control declining systematically with increasing retention intervals. On probe test trials, the presentation of the preparatory food event was preceded by a stimulus that had previously been paired (CS+) or unpaired with food (CS?). Discriminative responding to CSr was better following CS? than following CS+ in the unsignaled, but not the signaled, group. These results suggest that the enhanced retention following surprising preparatory events reflects a generalization decrement induced by changing the signaling conditions between training and testing. 相似文献