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1.
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
2.
Pigeons were trained in a delayed matching task in which the samples were short (2 sec) and long (10 sec) presentations of either a houselight or a keylight. Transfer trials involved short and long presentations of the nontrained signal as the sample. In the intermittent transfer test, infrequent transfer trials were intermixed with more frequent training trials; in the sustained transfer test, all trials were transfer trials. The intermittent test revealed only weak transfer. The sustained test revealed transfer in Session 1 only in birds that had received pairings of the transfer signal and food prior to testing. However, regardless of whether the transfer signal had been previously paired with food, birds exposed to consistent contingencies between duration and choice across training and testing learned the transfer task more rapidly than did birds exposed to inconsistent contingencies. It was concluded that some training in which the transfer signal serves as the sample is required before the durations of a transfer signal are related to the rules associating duration and responding 相似文献
3.
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
4.
Experiment 1 compared the acquisition of initial- and terminal-link responding in concurrent chains. The terminal-link schedules were fixed interval (FI) 10 sec and FI 20 sec, but some presentations were analogous to no-food trials in the peak procedure, lasting 60 sec with no reinforcement delivery. Pigeons completed a series of reversals in which the schedules signaled by the terminal-link stimuli (red and green on the center key) were changed. Acquisition of temporal control of terminal-link responding (as measured by peak location on no-food trials) was more rapid than acquisition of preference in the initial links. Experiment 2 compared acquisition in concurrent chains, using the typical procedure in which the terminal-link schedules are changed with a novel arrangement in which the initial-link key assignments were changed while the terminal-link schedules remained the same. Acquisition of preference was faster in the latter condition, in which the terminal-link stimulus-reinforcer relations were preserved. These experiments provide the first acquisition data that support the view that initial-link preference is determined by the values of the terminal-link stimuli. 相似文献
5.
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
6.
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
7.
Conditioned lick suppression in rats was used to explore the role of timing in trace conditioning. In Experiment 1, two groups of rats were exposed to pairings of a CS (CS1) with a US, under conditions in which the interstimulus interval (ISI) that separated CS1 offset and US onset was either 0 or 5 sec. Two additional groups were also exposed to the same CS1→US pairings with either a 0 or a 5-sec ISI, and then received “backward” second-order conditioning in which CS1 was immediately followed by a novel CS2 (i.e., CS1→CS2). A trace conditioning deficit was observed in that the CS1 conditioned with the 5-sec gap supported less excitatory responding than the CS1 conditioned with the 0-sec gap. However, CS2 elicited more conditioned responding in the group trained with the 5-sec CS1-US gap than in the group trained with the 0-sec CS1-US gap. Thus, the CS1-US interval had inverse effects on first- and second-order conditioned responding. Experiment 2 was conducted as a sensory preconditioning analogue to Experiment 1. In Experiment 2, rats received the CS1?CS2 pairings prior to the CS1→US pairings (in which CS1 was again conditioned with either a 0 or a 5-sec ISI). Experiment 2 showed a dissociation between first- and second-order conditioned responding similar to that observed in Experiment 1. These outcomes are not compatible with the view that differences in responding to CSs conditioned with different ISIs are mediated exclusively by differences in associative value. The results are discussed in the framework of the temporal coding hypothesis, according to which temporal relationships between events are encoded in elementary associations. 相似文献
8.
Timing of conditioned keypecking was investigated using a delay autoshaping procedure. In two experiments, the CS-US interval
(ISI) was varied and the temporal pattern of responding during unreinforced probe trials extending beyond the reinforced ISI
was recorded. Both experiments showed temporal control of keypecking at ISIs of 4, 8, and 16 sec, regardless of whether the
probe duration was held constant (Experiment 1) or covaried with the ISI (Experiment 2). Analyses showed that the timing of
keypecking was scalar. Increased responding near the end of the probe was due possibly to independent timing of the probe
duration. In a third experiment, a group of subjects trained at an ISI of 8 sec were extinguished by presentation of only
probe trials. Although the maximal response rate declined progressively, timing of keypecking did not change. 相似文献
9.
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
10.
Two experiments are reported on the elimination of autoshaped keypecking in pigeons by introducing added feedings that have the effect of removing the contingency between keylight (CS) and feedings. In Experiment 1, added feedings were signaled, by an already conditioned stimulus, in one group but not in another. Contrary to the Rescorla-Wagner theory, but consistent with scalar expectancy theory, responding in these groups declined at equal rates. In Experiment 2, following acquisition, some groups were exposed to repeated sessions in which they received feedings alone prior to receiving both CS and feedings noncontingently. Although prior exposure to feedings did reduce the total amount of responding in subsequent noncontingent sessions, it did not, contrary to scalar expectancy theory, reduce the initial level of responding to the CS. It is suggested that a differential between reinforcing conditions in the CS as compared with neighboring non-CS periods is more fundamental to conditioning than is acknowledged in the Rescorla-Wagner theory or in scalar expectancy theory. 相似文献
11.
Peter C. Holland 《Learning & behavior》2000,28(2):121-135
The effects of trial (T) and intertrial (I) durations were examined in two Pavlovian conditioning experiments with rats, in which a noise conditioned stimulus (CS)
was paired with food delivery. In Experiment 1,T was either 10 or 20 sec, andI ranged from 15 to 960 sec, in separate groups of rats. The acquisition rate and final level of conditioned responding showed
ratio invariance: They were better predicted by theI/T ratio than byI orT alone. In Experiment 2, theI/T ratio was 6.0 in all the groups, andT was 20, 40, 80, or 160 sec. Ratio invariance was not observed: Despite the commonI/T ratio, the rate of acquisition, final level of conditioned responding, and the ability of the CS to block conditioning of
another stimulus differed among the groups. At the same time, the temporal distribution of conditioned responding withinT was similar in all the groups throughout conditioning and extinction and showed superpositioning when normalized acrossT. Many but not all aspects of the data were consistent with scalar timing theory. 相似文献
12.
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
13.
In the present experiments, we investigated the effects of mindfulness on behavioral extinction and resurgence. Participants received instrumental training; either they received FI training (Experiment 1), or they were trained to emit high rates and low rates of response via exposure to a multiple VR yoked-VI schedule prior to exposure to a multiple FI FI schedule in order to alter their rates of responding learned during Experiment 2. Participants were then exposed to either a focused- (mindfulness) or an unfocused-attention induction task. All participants were finally exposed to an extinction schedule in order to determine whether a mindfulness induction task presented immediately prior to extinction training affected extinction (Experiment 1) and behavioral resurgence (Experiment 2). During the extinction phase, the rates of responding were higher in the control group than in the mindfulness group, indicating that the mindfulness group was more sensitive to the contingencies and, thus, their prior performance extinguished more readily (Experiment 1). Moreover, rates of response in the extinction components less precisely reflected previous training in the mindfulness group, suggesting less resurgence of past behaviors after the mindfulness induction (Experiment 2). 相似文献
14.
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
15.
Maes JH 《Learning & behavior》2003,31(4):332-348
In two experiments, the behavioral effects of different response-feedback contingencies were examined with a task requiring
human subjects to repeatedly type three-key sequences on a computer keyboard. In Experiment 1, the subjects first received
positive feedback for response variability, followed by no feedback, or vice versa. In Experiment 2, the subjects first received
positive feedback for response variability, followed by response-independent positive feedback, or vice versa. Response stability
and variability were examined using different measures, such as percentage of trials meeting the variability criteria, frequency
of use of the different response alternatives, and autocorrelations as an index of response randomness. The subjects’ behavior
in the first phase in each condition came to reflect the current feedback contingency. Depending on the measure examined,
responding after each contingency change was characterized by both response stability and decreases or increases in response
variability. The collective results are discussed in the framework of previous animal and human studies on behavioral stability
and variability. 相似文献
16.
Pigeons were trained to match temporal (2 and 8 sec of keylight) and color (red and green) samples to vertical and horizontal comparison stimuli. In Experiment 1, samples that were associated with the same correct comparison stimulus displayed similar retention functions; and there was no significant choose-short effect following temporal samples. This finding was replicated in Phase 1 of Experiment 2 for birds maintained on the many-to-one mapping, and it was also obtained in birds that had been switched to a one-to-one mapping by changing the comparison stimuli following color samples. However, in Phase 2 of Experiment 2, when the one-to-one mapping was produced by changing the comparison stimuli following temporal samples, a significant choose-short effect was observed. In Experiment 3, intratrial interference tests gave evidence of temporal summation effects when either temporal presamples or color presamples preceded temporal targets. This occurred even though these interference tests followed delay tests that failed to reveal significant choose-short effects. The absence of significant choose-short effects in Experiment 1 and in Phase 1 of Experiment 2 indicates that temporal samples are not retrospectively and analogically coded when temporal and nontemporal samples are mapped onto the same set of comparisons The interference test results suggest that the temporal summation effect arises from nonmemorial properties of the timing system and is independent of the memory code being used 相似文献
17.
Pigeons responded in a two-component peak procedure in which the components differed in terms of reinforcement magnitude (Experiment 1), immediacy (Experiment 2), or probability (Experiment 3). The prediction of behavioral momentum theory that responding in the relatively richer component should be more resistant to change was tested by (1) presenting response-independent food in the intervals between components according to a variable-time (VT) schedule, (2) prefeeding, and (3) extinction. In all the experiments, peak location in baseline occurred earlier, relative to the schedule value in the richer component. Peak response rate was more resistant to change in the richer component during the VT and prefeeding tests, and change in peak rate was more sensitive to differential reinforcement than change in overall response rate. Changes in measures of performance on peak trials during the disruptor tests were partially consistent with predictions of the behavioral theory of timing. The results suggest that peak response rate provides a more sensitive index of resistance to change for fixed-interval schedules than does overall response rate and that reinforcement strengthens both peak responding and temporal control. 相似文献
18.
Michael P. Browne 《Learning & behavior》1976,4(3):287-292
Following sessions of free grain delivery, a transparent shield was placed over the magazine, which made food unavailable. Different groups of pigeons then “observed” positive, zero, or negative correlations between the keylight and inaccessible grain. Keypecks were rare in all groups. Next, the shield was removed, and a transfer-test was given in which all subjects were exposed to keylight presentations followed by available grain. The previously positive group pecked sooner and more frequently than the others. A second experiment, which yielded similar results, excluded the possibility that approaches to the keylight during the observation phase had mediated learning in the first experiment. These findings were discussed in relationship to operant and Pavlovian analyses of autoshaping. 相似文献
19.
Within-session changes in responding during delayed matching-to-sample and discrimination procedures
Two experiments examined within-session changes in responding during discrimination procedures. In Experiment 1, rate of responding changed significantly within sessions during symbolic delayed matching-to-sample tasks when the delay between the stimulus and the choice period was short (1–5 sec), but not when it was long (8–12 sec). The percentage of responses that were correct did not change within sessions. In Experiment 2, response rates increased and then decreased within sessions during both S1 and S2 when successive discrimination procedures provided high, but not low, rates of reinforcement. Discrimination ratios sometimes increased within sessions. These results question two potential definitions of attention as explanations for within-session changes in response rates. They are more compatible with explanations based on concepts such as arousal, satiation, habituation, and interfering responses. 相似文献
20.
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