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1.
Acquisition to a target conditioned stimulus (CS) is prevented when extra, unsignaled unconditioned stimuli (USs) are presented with sufficient frequency to remove contingency between target CS and US. Acquisition occurs, however, when the extra USs are signaled by another CS. According to the Rescorla-Wagner theory, signaling reduces contextual conditioning, which otherwise prevents acquisition. Results of Experiment 1 led to the rejection of a rival explanation derived from scalar expectancy theory by showing that acquisition does not occur when only half of the extra USs are signaled. The results of Experiment 2 were, however, contrary to the Rescorla-Wagner theory because they showed equivalent acquisition when the stimulus used to signal the extra USs was also present concurrently with the target CS. Signaling may exert its effect by converting the intertriai interval to CS?. 相似文献
2.
Pavlov (1927/1960) reported that following the conditioning of several stimuli, extinction of one conditioned stimulus (CS) attenuated responding
to others that had not undergone direct extinction. However, this secondary extinction effect has not been widely replicated in the contemporary literature. In three conditioned suppression experiments with rats,
we further explored the phenomenon. In Experiment 1, we asked whether secondary extinction is more likely to occur with target
CSs that have themselves undergone some prior extinction. A robust secondary extinction effect was obtained with a nonextinguished
target CS. Experiment 2 showed that extinction of one CS was sufficient to reduce renewal of a second CS when it was tested
in a neutral (nonextinction) context. In Experiment 3, secondary extinction was observed in groups that initially received
intermixed conditioning trials with the target and nontarget CSs, but not in groups that received conditioning of the two
CSs in separate sessions. The results are consistent with the hypothesis that CSs must be associated with a common temporal
context during conditioning for secondary extinction to occur. 相似文献
3.
Pigeons pecked keys on concurrent-chains schedules that provided a variable interval 30-sec schedule in the initial link.
One terminal link provided reinforcers in a fixed manner; the other provided reinforcers in a variable manner with the same
arithmetic mean as the fixed alternative. In Experiment 1, the terminal links provided fixed and variable interval schedules.
In Experiment 2, the terminal links provided reinforcers after a fixed or a variable delay following the response that produced
them. In Experiment 3, the terminal links provided reinforcers that were fixed or variable in size. Rate of reinforcement
was varied by changing the scheduled interreinforcer interval in the terminal link from 5 to 225 sec. The subjects usually
preferred the variable option in Experiments 1 and 2 but differed in preference in Experiment 3. The preference for variability
was usually stronger for lower (longer terminal links) than for higher (shorter terminal links) rates of reinforcement. Preference
did not change systematically with time in the session. Some aspects of these results are inconsistent with explanations for
the preference for variability in terms of scaling factors, scalar expectancy theory, risk-sensitive models of optimal foraging
theory, and habituation to the reinforcer. Initial-link response rates also changed within sessions when the schedules provided
high, but not low, rates of reinforcement. Within-session changes in responding were similar for the two initial links. These
similarities imply that habituation to the reinforcer is represented differently in theories of choice than are other variables
related to reinforcement. 相似文献
4.
Two rat experiments were run to study the effects of a wide range of signal (CS) intensities on the suppression of licking. In Experiment 1, a light CS was varied over five levels, including zero intensity. Conditioned suppression was found to vary directly with CS intensity, but basal lick rates were not different among groups. In Experiment 2, an attempt was made to disturb the basal rate of licking, while a tone CS was varied over four levels, including zero intensity. Here the suppression of the CS rates was found to be directly related and basal rates inversely related to CS intensity. The results as a whole were consistent with the Perkins-Logan hypothesis regarding the effects of CS intensity upon conditioning, but not with the Rescorla-Wagner model of classical conditioning. 相似文献
5.
“Comparator” accounts of associative conditioning (e.g., Gibbon & Balsam, 1981; Miller & Matzel, 1988) suggest that performance to a Pavlovian CS is determined, by a comparison of the US expectancy of the CS with the US expectancy of general background cues. Recent research indicates that variation in the excitatory value of cues in the local temporal context of a CS may have a profound impact on conditioned responding to the CS (e.g., Kaplan & Hearst, 1982), implicating US expectancy based on local, rather than overall, background cues as the critical comparator term for a CS. In two experiments, an excitatory training context attenuated responding to a target CS. In Experiment 1, the context was made excitatory by interspersing unsignaled USs with target CS-US trials. In this case, posttraining extinction of the conditioning context restored responding to the target CS. In Experiment 2, the target CS’s local context was made excitatory by the placement of excitatory “cover” stimuli in the immediate temporal proximity of each target CS-US trial. In this experiment, posttraining extinction of the proximal cover stimuli, not extinction of the conditioning context alone, restored responding to the target CS. An observation from both experiments was that signaling the otherwise unsignaled USs did not appear to influence the associative value of the conditioning context. The results are discussed in relation to a local context version of the comparator hypothesis and serve to emphasize the importance of local context cues in the modulation of acquired behavior. Taken together with other recent reports (e.g., Cooper, Aronson, Balsam, & Gibbon, 1990; Schachtman & Reilly, 1987), the present observations encourage contemporary comparator theories to reevaluate which aspects of the conditioning situation comprise the CS’s comparator term. 相似文献
6.
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
7.
In Experiment 1, three groups of pigeons were autoshaped and then administered one of three different response-elimination procedures. Group TRC (truly random control) and Group Backward (backward conditioning) ceased responding more rapidly than Group CS-only. In a subsequent reacquisition test with a novel CS, Groups TRC and Backward were retarded relative to Group CS-only. In Experiment 2, the CS-only and TRC response-elimination treatments were not differentially effective in extinguishing the response. The treatments were followed either by five sessions of unpredictable US presentations (US-only) or by five sessions of remaining in their home cages (hold) prior to the reacquisition test. The TRC treatment retarded reacquisition relative to the CS-only treatment; the US-only posttreatment manipulation failed to reliably retard reacquisition relative to Hold, although retarding effects of US-only are discernible in a block-by-block analysis. Applications and limitations of a context-blocking account of these results are discussed. 相似文献
8.
The blocking phenomenon was investigated in the sexual response system of male Japanese quail. Access to a live female quail served as the unconditioned stimulus (US). The same audiovisual cue served as the pretrained stimulus in all of the experiments. Following asymptotic conditioning of the audiovisual cue, a second conditioned stimulus (CS2) was added. In Experiment 1, CS2 was a rectangular wood block that had little or no resemblance to a female quail and could not support copulatory behavior. In Experiment 2, CS2 was a terrycloth object that had no quail parts but could support copulatory behavior, and, in Experiment 3, CS2 was a terrycloth object that had a taxidermically prepared head of a female quail added. The terrycloth-only object supported more rapid conditioning than did the wood block, but the blocking effect was obtained with both kinds of stimuli. Approach responding to the terrycloth + head object required pairing it with copulatory opportunity, and the terrycloth + head object supported at least as rapid conditioning as did the terrycloth-only object. However, responding to the terrycloth + head object was not blocked by the pretrained audiovisual cue. These results indicate that the blocking effect occurs in sexual conditioning even with stimulus objects that can support copulation. However, the addition of species-typical head cues to an object makes that object such a powerful stimulus that conditioned approach responding to it cannot be blocked by a previously conditioned arbitrary audiovisual cue. 相似文献
9.
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
10.
Little responding develops to a conditioned stimulus (CS) that is placed in a random relation to an unconditioned stimulus (US). However, if the USs not preceded by that CS are themselves signaled by another stimulus, then the CS does come to elicit responding. This result has been attributed (e.g., by Durlach, 1983) to the signal’s blocking of conditioning to background cues that otherwise would prevent conditioning of the CS. However, Goddard and Jenkins (1987) have suggested the alternative that signaling the USs promotes responding due to the adventitious creation of periods of signaled nonreinforcement. Two experiments were conducted to assess this alternative, involving an autoshaping preparation in pigeons. In Experiment 1, little responding to a keylight CS presented in a random relation to a food US occurred, despite the explicit presentation of a discrete noise signaling periods of no food in the intertrial interval (ITI). Experiment 2 was designed to replicate the procedure of Goddard and Jenkins, in which an auditory stimulus extended throughout the ITI of a random schedule, terminating only prior to extra USs and during the CS. Contrary to their findings, little responding developed to the target CS. However, responding did develop when the sound-free period occurred only prior to the extra USs. These results offer little support for the hypothesis that signaled periods of nonreinforcement promote responding on random schedules. However, they are consistent with the view that signaling of ITI USs acts by preventing conditioning of potentially competitive background cues. 相似文献
11.
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
12.
Dale Swartzentruber 《Learning & behavior》1993,21(1):14-22
Two autoshaping experiments with pigeons examined contextual control of responding to conditioned stimuli (CSs) when separate phases of reinforcement and nonreinforcement occurred in different contexts. In Experiment 1, a CS was first conditioned in Context A prior to nonreinforcement in Context B. In Experiment 2, a conditional discrimination reversal procedure was employed in which one CS was first reinforced in A prior to nonreinforcement in B, and another CS was first nonreinforced in A and then reinforced in B. In both experiments, the extent of contextual control was assessed by testing the CSs in A and B. The CS specificity of control was assessed by examining control of CSs that had been treated like the original CSs, but in a different pair of contexts. The results show that contexts control responding to CSs through a CS-specific mechanism, as well as through a mechanism that is independent of the identity of the CS. However, the extent to which control is mediated by a CS-independent mechanism depends on the training history of the CS. 相似文献
13.
In two experiments, we examined two related conditioning problems previously investigated by Red-head and Pearce (1995a) and Pearce, Aydin, and Redhead (1997). Experiment 1 involved an A+, B+, C+, AB+, AC+, BC+, ABC2 discrimination. The Rescorla-Wagner model predicts that response to AB, AC, and BC will be greater than that to A, B, and C at asymptote, whereas the Pearce model makes the opposite prediction. In Experiment 2, we investigated the responding to a novel ABC compound in groups trained with either A+, B+, C+ or AB+, AC+, BC+. The Rescorla-Wagner model predicts greater response to ABC in the group trained with A+, B+, C+ than in the group trained with AB+, AC+, BC+, whereas the Pearce model makes the opposite prediction. In contrast to the findings of Redhead and Pearce (1995a) and Pearce et al. (1997) in pigeon autoshaping, our findings in rabbit eyelid conditioning support the Rescorla-Wagner model. 相似文献
14.
Experiment 1 compared the acquisition of a feature-positive and a feature-negative discrimination in humans. In the former, an outcome was signaled by two stimuli together, but not by one of these stimuli alone. In the latter, the outcome was signaled by one stimulus alone, but not by two stimuli together. Using a within-group design, the experiment revealed that the feature-positive discrimination was acquired more readily than the feature-negative discrimination. Experiment 2 tested an explanation for these results, based on the Rescorla-Wagner theory, by examining how novel discriminations, based on a combination of a feature-positive and a feature-negative discrimination, were solved. The results did not accord with predictions from the theory. Alternative explanations for the results are considered. 相似文献
15.
Two experiments are described, which involved the investigation of interactions between the nature of the conditioned stimulus (CS) and the nature of the unconditioned stimulus (UCS) in producing signal-centered behavior. In Experiment 1, rats received response-independent heat reinforcement in a cold environment. For some groups, this heat UCS was signaled by presentations of a standard aluminum retractable lever; for other groups, it was signaled by a retractable lever covered in acrylic fur (furry lever CS). Only the subjects that received the furry lever CS paired with heat exhibited differential CS-contact behavior, when compared with unpaired, aluminum lever, and warm control subjects. In Experiment 2, hungry rats received pairings of either an aluminum or a furry lever with food (UCS). When compared with unpaired controls, only the subjects that received the aluminum lever paired with food showed differential signal-directed behavior; the subjects receiving the furry lever CS did not show differential contact with the CS, but instead exhibited differential food tray entry behavior during CS presentation. In the two studies, the signal-directed behavior exhibited by subjects resembled either thermoregulatory or feeding behaviors characteristic of rats. The results suggest that signal-directed behavior is determined by a complex interaction between the ecological relevance of the CS and the nature of the UCS—an interaction that can best be described in terms of a behavior systems model of conditioned responding. 相似文献
16.
The acquisition of the rabbit’s nictitating membrane response to a tone + light compound and its components was examined as a function of the CS-US interval (Experiment 1) and CS duration (Experiment 2). In Experiment 1, responding to the compound attained high levels in all groups, but responding on component test trials declined to low levels as the CS-US interval increased across values of 300, 800, and 1,300 msec. Further disparities between the compound and components appeared when the animals were shifted to a positive patterning schedule. In Experiment 2, disparities between the compound and components increased as the duration of the CS was increased across values of 50, 200, and 800 msec within a fixed CS-US interval of 800 msec. The results are discussed with respect to distributive processes, configuration, and speed-accuracy tradeoffs. 相似文献
17.
The present research examined the temporal distribution of responding in a lick suppression paradigm. In Experiment 1, rats were trained with either a 30- or a 120-s conditioned stimulus (CS), which was followed either by a footshock (unconditioned
stimulus [US]) or nothing. Licking during the CS was suppressed only in the former condition. Suppression was more pronounced
early in the CS. In Experiment 2, rats were exposed to two 30-s or two 120-s CSs, with delivery of the shock being contingent on CS1 for half of the animals
and on CS2 for the other half. For both the paired and the unpaired conditions, suppression at the beginning of CS1 was observed
for all the groups. By discounting the possibility of generalization between CS1 and CS2, it appears that this initial suppression
was not a conditioned response to the CS, but an unconditioned one due to mere exposure to the shock US. 相似文献
18.
Three experiments with rat subjects examined the development of simultaneous and serial feature-positive discriminations in appetitive conditioning. In Experiment 1, reinforced presentations of a simultaneous light-tone compound were intermixed with nonreinforced presentations of either the light or the tone. The compound stimulus acquired conditioned behaviors of a form characteristic of the predictive feature alone; the element common to reinforced and nonreinforced trials did not evoke conditioned behavior. In Experiment 2, reinforced presentations of a serial light-trace-tone compound were intermixed with nonreinforced tone-alone presentations. The light feature stimulus acquired conditioned behaviors characteristic of visual CSs. The tone stimulus, common to reinforced and nonreinforced trials, evoked conditioned behaviors characteristic of auditory CSs, but only when preceded by the light. In Experiment 3, variations in the interval between the light and tone on reinforced trials had little effect on responding to the light CS but substantially altered the pattern of responding to the tone CS. These results suggested that simultaneous and serial feature-positive discriminations may be solved differently. Performance in simultaneous feature-positive discriminations may be determined solely by associations between the feature stimulus and the reinforcer, but performance in serial discriminations may also involve the acquisition of a conditional cue function to the feature. 相似文献
19.
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
20.
Conditioned suppression in rats is often unaffected when the context (or set of background stimuli) is changed following conditioning. This suggests that responding to the conditioned stimulus (CS) can be relatively insensitive to the context in which the CS is presented. In two experiments, we examined whether sensitivity to contextual stimuli is affected by preexposure to the CS. In Experiment 1, when the CS was novel at the outset of conditioning, conditioned suppression was not affected when the context was changed following conditioning. However, when the CS had been preexposed, responding was weaker when extinction occurred outside of the conditioning context. In Experiment 2, responding was again sensitive to the test context, regardless of whether preexposure occurred in the conditioning context or in an alternate context. These results suggest that the extent to which responding is sensitive to context can depend on the conditioning history of the CS. 相似文献