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1.
Two experiments were conducted to investigate functional similarities between “hunger CRs” of Konorski’s (1967) model of appetitive classical conditioning and sign-tracking behavior in rats. Konorski’s model predicts that hunger CRs will be facilitated (1) when a nonrein-forced stimulus similar to the reinforced CS is introduced, and (2) when some CS presentations are unexpectedly nonreinforced. In Experiment 1, hungry rats acquired a leverpress response to a retractable lever that was paired with response-independent food. Following this training, a second lever was introduced whose presentation was not followed by food. The effect of the presence of this second lever was to facilitate responding to the original lever. In Experiment 2, single-lever autoshaping training was followed by a shift from 100% pairing of the lever with food to only 50% of the lever presentations being followed by food. The introduction of partial reinforcement produced an immediate and durable increase in leverpressing. The findings of both experiments are consistent with predictions from Konorski’s model of classical conditioning if sign-tracking is considered as a “hunger CR.” 相似文献
2.
The experiments reported in the present study tested whether decreasing intertrial intervals (ITIs) intensifies the disruptive
effects of increasing retention intervals (RIs) in a delayed conditional discrimination by decreasing the animal’s trial tracking
accuracy (Cohen & Armstrong, 1996; Cohen & Roberts, 1996). Rats responded on a fixed ratio (FR) 1 or fixed interval (FI) 10-sec
reinforcement schedule at a second light or tone stimulus, S2, when the first light or tone stimulus, S1, had signaled an
FI 10-sec or FR 1 schedule, respectively. RIs between S1 and S2 were increased from 3 to 24 sec and never exceeded ITIs that
were reduced from 24 to 6 sec. For some rats, the trials were separated from each other by extending the lever at S1 and retracting
it at the end of S2 (ITI lever-retracted group). For other, control rats, the lever remained extended throughout the session
(lever-extended group, Experiment 1) or was extended and retracted with the onset and offset of each stimulus (RI/ITI lever-retracted
group, Experiment 2). The rats under all trial conditions learned to delay leverpressing on the FI 10-sec schedule. Latency
to begin leverpressing on the FI 10-sec schedule declined as RIs were increased, but this effect was attenuated in the ITI
lever-retracted groups in both experiments, as would be predicted by thetrial tracking hypothesis. Decreasing ITIs from 24 to 6 sec intensified the disruptive effects of increasing RIs from 3 to 6 sec in the
RI/ITI lever-retracted group (Experiment 2), as would be predicted by the trial tracking hypothesis. 相似文献
3.
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
4.
A series of experiments was performed to determine whether sign-tracking would occur in rats with intravenous (i.v.) cocaine
as the unconditioned stimulus. In Experiment 1, a retractable lever paired with food produced strong sign-tracking, but a
lever paired with one of three doses of i.v. cocaine did not elicit any approach or contact behavior. Experiment 2 demonstrated
that doses of cocaine that did not elicit sign-tracking would function as a positive reinforcer for a lever contact operant.
In Experiment 3, an artificialconsummatory response was added to make the cocaine reinforcement episode more behaviorally comparable to that occasioned by food. Although the
rats readily performed this response when it was required to receive cocaine infusions, they still did not contact a lever
that signaled the availability of these infusions. It appears that cocaine is different from other positive reinforcers (e.g.,
food, water, warmth, or intracranial stimulation) in that it will not produce sign-tracking in rats. 相似文献
5.
In Experiment 1, rats were trained to leverpress on a variable ratio (VR) 30 schedule with a 500-msec delay between the reinforced response and food delivery. Subjects that experienced a signal during the delay responded faster than did control subjects that received the stimulus un-correlated with reinforcement. Higher response rates were obtained when the stimulus used to signal reinforcement was auditory rather than visual. Experiments 2 and 3 compared the effects of signaling reinforcement with either a localized or a diffuse light on responding maintained by VR schedules of reinforcement. Elevated response rates were observed with the diffuse stimulus, but the localized stimulus failed to produce such potentiation. Experiment 3 also examined the conditioned reinforcing power of localized and diffuse visual stimuli. These results are discussed with reference to (1) theories of selective association and sign tracking and (2) their implications for current theories of signaling reinforcement. 相似文献
6.
In Experiment 1, it was shown that generalization testing following successive discrimination training between two closely spaced wavelengths results in a sharp gradient with a peak of responding shifted from S+ so as to be further removed from S?. Testing after a 24-h delay resulted in a flatter gradient with greater peak (and area) shift. A 5-min pretest exposure to S+, reinforced or unreinforced, or to S? (unreinforced) reinstated immediate test performance; free reinforcement with no discriminative stimulus present had no such effect. Experiment 2 replicated the flattening of generalization gradients and enhanced peak shift in delayed testing. Free feeding in a pretest treatment with a distinctive food uniquely associated with the wavelength discrimination problem failed to reinstate immediate test performance. Experiment 3 tested the hypothesis that free feeding failed as a reactivation treatment because it did not engender keypecking. Subjects were trained to peck a vertical line stimulus before being given wavelength discrimination training. Again, the enhanced peak shift and greater flattening with delayed wavelength generalization testing was found. A pretest exposure to the vertical line stimulus elicited pecking but had no effect on subsequent wavelength generalization. Thus, only a reactivation treatment that included one of the discrimination training stimuli was effective in producing delayed test performance comparable to that obtained in an immediate test. 相似文献
7.
Rats’ leverpressing was reinforced on variable-ratio (VR) schedules. As ratio values increased, response rates initially increased with them, then eventually decreased. In Experiment 1, rates were uniformly higher with one-pellet reinforcers than with two-pellet reinforcers—theparadoxical incentive effect. Killeen’s (1994) mathematical principles of reinforcement (MPR) described the data quantitatively but failed to predict the advantage for the one-pellet condition. In Experiment 2, rats received one-, two-, and three-pellet reinforcers with counterbalanced preloads of pellets; the continued superiority of the smaller reinforcers ruled out a satiation explanation. Experiment 3 introduced a 20-sec intertrial interval (ITI), and Experiment 4 filled the ITI with an alternate response to test a memorial/overshadowing explanation. In Experiment 5, the rats received one or two standard grain pellets or one sucrose pellet as reinforcers over an extended range of ratios. Once again, rates were higher for one than for two pellets at short to moderate VR values; thereafter, two pellets supported higher response rates. The diminution of the effect in Experiment 3 and its reversal in Experiment 4 and in Experiment 5 at large ratios provided evidence for overshadowing and reconciled the phenomenon with MPR. 相似文献
8.
In four experiments, we examined how the spatiotemporal proximity to food of the two elements of a serial conditioned stimulus (CS) influenced the pattern of CS-directed versus food-site-directed behavior in rats. Experiment 1 showed that only temporal proximity affected responding when the serial CS consisted of two successive 4-sec presentations of either a spatially near or a spatially far lever (NN or FF). However, Experiment 2 showed that behavior depended markedly on whether rats received a near followed by a far lever (NF) or a far followed by a near lever (FN). Experiment 3 showed that the effects of Experiment 2 could be changed by increasing the duration of the second CS element, and Experiment 4 showed that these changes were not related to previous training. We concluded that behavior produced by the spatiotemporal qualities of the lever elements can be attributed to a mapping between the temporal qualities of the CS elements and an underlying sequence of search modes related to finding food. 相似文献
9.
Eight food-deprived Wistar rats developed stable patterns of lever pressing and licking when exposed to a fixed-time 30-s schedule of food pellet presentation. The rats were trained to lever press by presenting the lever 10 s before the programmed food delivery, with the food pellet being delivered immediately upon a lever press. The operant contingency was then removed and the lever was inserted through the entire interfood interval, being withdrawn with food delivery and reinserted 2 s later. On successive phases of the study, a protective contingency postponed food delivery if responses (lever presses or licks) occurred within the last 1, 2, 5, 10, 20, or 25 s of the interfood interval. Lever pressing was reduced at much shorter response–food delays than those that reduced licking. These results demonstrate that reinforcement contributes to the maintenance of different response patterns on periodic schedules, and that different responses are differentially sensitive to delays. 相似文献
10.
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
11.
In three experiments, we examined the effects of signaling reinforcement during operant responding in order to illuminate the factors underlying instrumental overshadowing and potentiation effects. Specifically, we examined whether signaling reinforcement produces an enhancement and attentuation of responding when the response-reinforcer correlation is weak and strong, respectively. In Experiment 1, rats responded on variable-ratio (VR) or variable-interval (VI) schedules that were equated for the number of responses emitted per reinforcer. A signal correlated with reinforcement enhanced response rates on the VR schedule, but attenuated response rates were produced by the signal on the VI schedule. In Experiment 2, two groups of rats responded on a VI schedule while the two other groups received a conjoint VI, negative fixed-ratio schedule in which the subjects lost the availability of reinforcements if they emitted high response rates. A reinforcement signal attenuated responding for the simple VI groups but not for the animals given the negative fixed-ratio component, although the signal improved response efficiency in both groups. In Experiment 3, a poor correlation between responding and reinforcement was produced by a VI schedule onto which the delivery of response-independent food was superimposed. A signal for reinforcement initially elevated responding on this schedule, relative to an unsignaled condition; however, this pattern was reversed with further training. In sum, the present experiments provide little support for the view that signaling reinforcement enhances responding when the response-reinforcer correlation is weak and attenuates responding when this correlation is strong. 相似文献
12.
Alfred V. Bacotti 《Learning & behavior》1976,4(1):41-44
Eleven rats were exposed to a multiple variable-interval 1-min variable-interval 1-min schedule of reinforcement. All rats were initially fed a daily ration of food in the home cages immediately after the end of each session. In a later phase of the experiment, the same amount of food was fed 1 h after the end of each session. Later, five rats were again fed immediately after each session. Amount of food received and deprivation level in terms of percent of free feeding weight were constant across conditions. Response rates decreased within each session under immediate feeding. When feeding was delayed, rates in each component of the multiple schedule increased throughout the session and the decreasing trends were generally eliminated. The results suggest that home cage feeding time, apart from changes in deprivational level, is an important variable in the control of behavior in experimental sessions. 相似文献
13.
Five rats responded on several concurrent schedules in which pressing a key produced reinforcers in one component and pressing a lever produced reinforcers in the other component (Experiment 1). Four pigeons responded on several concurrent keypeck treadlepress schedules (Experiment 2). The programmed rates of reinforcement varied from 15 to 240 reinforcers per hour in different conditions. Rates of responding usually changed systematically within experimental sessions, and the changes were similar for the two components of a concurrent schedule. These results imply that within-session changes in responding may not confound the predictions of theories that describe the ratio of the rates of responding during the two components of concurrent schedules. Instead, within-session changes may be controlled by a mechanism that integrates the reinforcers obtained from the two components. 相似文献
14.
Reed P 《Learning & behavior》2006,34(4):379-386
Three experiments were performed to examine the effect of response force on rats’ performance on various schedules of reinforcement.
Response force was manipulated by changing the weight of the lever in the operant chamber—a heavy lever for high response
force and a light lever for low response force. Using a within-subjects design, Experiment 1 replicated previous findings
that rats respond more quickly on variable ratio (VR) than on equivalent variable-interval-plus-linear-feedback (VI+) schedules.
Experiment 2 replicated this finding but also showed that the use of a smaller response force abolished the response rate
difference between the VR and VI+ schedules. Experiment 3 used a between-subjects design and showed a response rate difference
between the VR and VI+ schedules with a high response force but no response rate difference with a low response force. This
suggests that under conditions of low force, when the rats’ responding can continue at prolonged high rates, these subjects
show little difference in their response rates between VR and VI+ schedules. These data are similar to those found for human
subjects. 相似文献
15.
The conditions under which circadian and interval-timing mechanisms are used in time-place discrimination were investigated.
Rats earned the first daily meal by pressing a lever beginning 3.5 h after the start of the session and a second daily meal
by pressing another lever. The second meal started 3.5 or 7 h (Experiment 1) or 0.75 or 1.75 h (Experiment 2) after the start
of the first meal, using independent groups. In Experiment 1, approximately half of the rats used an interval-timing mechanism,
and the other half used a circadian mechanism. In Experiment 2, the rats timed two intervals, one from the start of the session
until the first meal and the other from the first to the second meal. A circadian mechanism is relevant to timing intervals
in the range of 1.75–3.5 h, and an interval-timing mechanism can be used to time intervals from 0.75–7 h. 相似文献
16.
Male and female Wistar rats were trained in a delayed matching-to-position procedure in which one of the two levers (sample) was presented. Pressing this lever resulted in its retraction and began a delay interval of random variable duration, which terminated with the occurrence of the first nose poke in the pellet retrieval unit after the delay interval had expired. Both levers were then inserted into the chamber, and food became available when the subject pressed the lever that had previously been pressed (matching response). When the subject failed to make a matching response, time out (5 sec) was presented. In the next experimental condition, nonmatching was reinforced. Males and females required an equal number of trials to attain 80% accuracy during three consecutive sessions under matching and nonmatching conditions. Response accuracy decreased as the delay interval increased, during both conditions. Differences between the sexes were not observed, suggesting that memory functions in male and female rats may only differ when other behavioral differences between the sexes are allowed to interfere with the assessment of memory functioning. 相似文献
17.
The current four experiments investigated gaze following behavior in response to gaze and head turns in 4-month-olds and how reinforcement learning influences this behavior (N = 99). Using interactive eye tracking, infants’ gaze elicited an animation whenever infants followed a person’s head or gaze orientation (Experiment 1.1, 2.1 and 2.2) or looked at the opposite side (Experiment 1.2). Infants spontaneously followed the direction of a turning head with and without simultaneously shifted gaze direction (Cohen’s d: 0.93–1.05) but not the direction of isolated gaze shifts. We only found a weak effect of reinforcement on gaze following in one of the four experiments. Results will be discussed with regard to the impact of reinforcement on the maintenance of already existing gaze following behavior. 相似文献
18.
Increasing Steps in Recall of Events: Factors Facilitating Immediate and Long-Term Memory in 13.5- and 16.5-Month-Old Children 总被引：2，自引：0，他引：2
Children late in the second year of life show patterns of event recall similar to those of older children: (a) well-ordered immediate and delayed recall, and (b) facilitation of recall by familiarity and by enabling relations. We used elicited imitation to test whether the patterns extend to children early in the second year. In Experiment 1, 13.5- and 16.5-month-olds accurately recalled familiar and novel 2-act sequences immediately and after a 1-week delay. For 16.5-month-olds, recall was facilitated by familiarity and by enabling relations; for 13.5-month-olds, only enabling relations facilitated recall. In Experiment 2, verbal cues were used to test immediate and 1-week delayed recall of 3-act sequences. For both ages, recall was facilitated by familiarity and by enabling relations. Experiment 3 verified that the verbal information served to cue recall of previously experienced events, not to "suggest" sequences that could be performed. Together the results demonstrate that children as young as 13 months can recall specific events after a delay. They also suggest development in sensitivity to factors that facilitate recall. 相似文献
19.
Paul T. P. Wong 《Learning & behavior》1978,6(1):82-93
Three runway experiments tested a stage model of extinction which postulated an orderly succession of three qualitatively different stages: habit, trial and error, and resolution. The model predicted that Stage 1 should be characterized by perseveration of habitual routes (i.e., response persistence) and the absence of competing responses; Stage 2, by an increase in investigatory behavior (response variation and hole exploration) and biting behavior; Stage 3, by a decrease in the competing responses of Stage 2 and continued increase in goal avoidance and substitution behavior (e.g., sand-digging). These predictions were largely confirmed. Further, Experiments 1 and 2 showed that, as expected by the model, continuous reinforcement (CRF) resulted in more practice of habitual routes in acquisition and greater response persistence, while partial reinforcement (PRF) resulted in more route variation and hole exploration in acquisition and greater goal persistence which was attributable to prior reinforcement of a trial-and-error coping strategy. Results of Experiment 3, which combined training trials and reward magnitudes orthogonally, supported the prediction that response persistence was positively related to training trials, and goal persistence negatively related to reward magnitudes. All three experiments demonstrated an inverted-U function in investigatory and biting behavior, as predicted by the stage model. 相似文献
20.
Frans van Haaren 《Learning & behavior》1981,9(3):425-431
The effects of changeover delays of fixed or variable duration on concurrent variable-interval performance in pigeons were investigated in a series of three experiments. Experiment 1 compared the effects of a fixed, variable, or variable signaled changeover delay on interchangeover times and responding during and after the changeover delay. The duration of the changeover delays was systematically varied in Experiment 2, and the relative reinforcement frequencies were manipulated in Experiment 3. Interchangeover times were found to be shorter when changeover delays of variable duration were compared with those of fixed duration. Changeover delays of fixed duration produced higher response rates during the changeover delay than after the changeover delay had elapsed; changeover delays of variable duration produced such differences to a lesser extent. It was concluded that the changeover delay in concurrent variable-interval schedules of reinforcement functionally acts as a delay period to the next opportunity for reinforcement, possibly serving as a conditioned reinforcer for the behavior preceding it (the interchangeover time) and as a discriminative stimulus for the behavior in its presence (response rates during the delay). 相似文献