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1.
Pigeons were studied on multiple variable-ratio yoked-variable-interval schedules in which components had equal rates of food reinforcement and appeared equally often on each of two keys. Interpolated between component changes on the final multiple schedule were 10-sec probes in which both schedule stimuli were present, one on each key. During multiple schedule training, variable-ratio response rates were greater than yoked-variable-interval rates; however, response rate differences in the components were not a function of the mean ratio value for the 40-to-320-ratio range studied. During the choice probes, subjects responded more to the stimulus associated with the interval schedule than to the one associated with the ratio schedule. It was concluded that pigeons prefer interval schedules over equal reinforcement rate ratio schedules, because the former generate fewer responses per reinforcement. 相似文献
2.
Four pigeons were exposed to several nonindependent concurrent variable-interval schedules of reinforcement. One schedule component required a keypecking response; the other component required a treadlepressing response. The birds matched the ratio of their behavior (as measured by responses and time) between the two topographically different responses to the ratio of reinforcement in those two components. When additional foods not contingent on a keypeck or treadle-press were then added, the birds matched time spent in the components to total rates of food delivered in those components; response matching was somewhat disrupted. The matching law, developed under concurrent variable-interval schedules requiring similar responses, can thus account for choice behavior involving topographically different responses. 相似文献
3.
Four of five pigeons were conditioned to peck a key at a high, stable rate on a VI schedule and then given concurrent access to free food. It was found, in replication of Neuringer’s results, that the pigeons pecked a key for grain in the presence of free grain. When availability of the response key (high-probability response) was made contingent on eating free grain (a lower probability response), there was a progressive increase in free-food eating, confirming Premack’s reinforcement principle. For two additional birds, when availability of the key was made contingent onnot eating the free food (a type of DRO schedule), the frequency of free-food eating declined. Thus, availability of the key. depending on the contingency, reinforced both the eating and noneating of free food. 相似文献
4.
Terry W. Belke 《Learning & behavior》1992,20(4):401-406
Four pigeons were exposed to multiple schedules with concurrent variable interval (VI) components and then tested for preference transfer. Half of the pigeons were trained on a multiple concurrent VI 20-sec, VI 40-sec/cuncurrent VI 4G-sec5 VI 80-sec schedule. The remaining pigeons were trained on a multiple concurrent VI 80-sec, VI 40-sec/concurrent VI 40-sec, VI 20-sec schedule-After stability criteria for time and response proportions were simultaneously met, four preference transfer tests were conducted with the stimuli associated with the VI 40-sec schedules. During the transfer tests, each pigeon allocated a greater proportion of responses (M=0,79) and time (M=0.82) to the stimulus associated with the VI 40-sec schedule that was paired with the VI 80-sec schedule than lo the VI 40-sec schedule stimulus paired with the VI 20-sec schedule. Absolute reinforcement rates on the two VI 40 sec schedules were approximately equal and unlikely to account for the observed preference. Nor was the preference consistent with the differences in local reinforcement rates associated with the two stimuli. Instead, the results were interpreted in terms of the differential value that stimuli acquire as a function of previous pairings with alternative schedules of reinforcement. 相似文献
5.
6.
Food- and water-deprived pigeons keypecked for food or water reinforcement on alternate trials. Under one condition, explicit stimuli on the key provided information about the trial outcome; under another condition, only the alternation schedule provided this information. Latency and/or response rate differences between food- and water-rewarded trials emerged during both conditions. Response topography also differed on food- and water-rewarded trials. These differences, as revealed by duration and force measurements of the keypeck and by human ratings of the pecking responses as being water- or food-related, were anticipatory in nature. These results not only extend previous work on reward alternation and reward-specific response topographies, but also have implications for theories of animal memory. In particular, these results are amenable to memory models that assume that an animal “codes” information that later must be recalled. 相似文献
7.
Tokens were given to university students in two separate experiments for participation in small group discussions. In the first experiment a multiple baseline design was used with two small groups in an educational psychology class. In the second, 10 small groups were assessed on group participation without and with a token condition. Results of the first experiment were inconclusive though favorable; the second experiment resulted in a significant difference (t=15.41; P<.001, df=77) in group participation when tokens were delivered contingent upon group participation. The results indicate that token technology can be an effective technique to increase small group participation when a variety of back-up reinforcers is offered. The results are discussed in terms of possible applications of token technology within a university setting. 相似文献
8.
Behavior reduced as a consequence of extinction or intervention can relapse. According to behavioral momentum theory, the extent to which behavior persists and relapses once it has been eliminated depends on the relative training reinforcement rate among discriminative stimuli. In addition, studies of context renewal reveal that relapse depends on the similarity between the training stimulus context and the test stimulus context following disruption by extinction. In the present experiments with pigeons, we arranged different reinforcement rates in the presence of distinct discriminative stimuli across components of a multiple schedule. Following extinction, we attempted to reinstate responding in the presence of those target components with response-independent food presentations. Importantly, we arranged the reinstating food presentations either within the target components or in separate components, either paired with extinction (Experiment 1) or reinforcement (Experiment 2) during baseline. Reinstatement increased with greater training reinforcement rates when the reinstating food presentations were arranged in the target components and the separate components paired with reinforcement during training. Reinstatement was smaller and was not systematically related to training reinforcement rates in the target components when reinstating food presentation occurred in separate components paired with extinction. These findings suggest that relapse depends on the history of reinforcement associated with the discriminative stimuli in which the relapse-inducing event occurs. 相似文献
9.
After rats were trained on a multiple schedule with variable interval 30-sec reinforcement in both stimulus components, omission, yoked, and extinction procedures were applied in S? while the variable interval continued in S+. In S?, omission training reduced response rate faster and to a lower terminal level than either response-independent yoked reinforcement or extinction, which were approximately equivalent. In S+, the extinction group exhibited elevated response rates representing behavioral contrast, while the omission and yoked groups showed reduced response rates. These results attest to the effectiveness of omission training as a response elimination method. They also contradict theories which posit reduction of response rate in S? to be necessary and sufficient for behavioral contrast. 相似文献
10.
Four pigeons pecked for food reinforcement on variable interval 1-min schedules and on the variable-interval 1-min components of multiple, concurrent, and pseudoconcurrent schedules. The pseudoconcurrent schedule provided only one schedule of reinforcement; but, any reinforcer could be collected by responding on either of two keys. The rate of responding generated by the variable interval schedule was not greater than the rates of responding generated by the components of the complex schedules. But, the rate of reinforcement obtained from the variable interval schedule was greater than the rates of reinforcement obtained from the components of the multiple schedule. These results may contradict the equation proposed by Herrnstein (1970). The equation predicts that the rate of responding generated by a schedule of reinforcement will be greater when the schedule appears alone, than when it appears as one component of a complex schedule. 相似文献
11.
Frances K. McSweeney 《Learning & behavior》1975,3(3):264-270
Five pigeons pecked for food reinforcement on several concurrent schedules. Their body weights were varied from 80% to 110% of their free-feeding weights. A number of predictions of the equations proposed by Herrnstein (1970) were tested. As predicted, the relative rate of responding equalled the relative rate of reinforcement for all subjects, on all schedules, at all body weights. And, as predicted, the overall rates of responding on the components of a concurrent schedule were slower than the local rates of responding on the components of an identical multiple schedule. Contrary to prediction, the total rate of responding generated by the concurrent schedules did not increase with increases in the total rate of reinforcement they provided. And, contrary to prediction, the k parameter did not remain constant, and the R0 parameter did not increase with increases in body weight. It was concluded that Herrnstein’s matching law and his interpretation of the m parameter are correct but that the interpretations of k and R0 require further investigation. 相似文献
12.
Rats and pigeons responded for food delivered according to multiple schedules. The session length varied from 10 to 120 min, and the programmed rate of reinforcement varied from 15 to 240 reinforcers per hour. Response rates usually changed systematically within experimental sessions. For both rats and pigeons, responding reached a peak after an approximately constant amount of time since the beginning of the session, regardless of session length. When rats, but not pigeons, served as subjects, the peak rates of responding occurred later in the session and the within-session changes were smaller for lower than for higher rates of reinforcement. The similarities between the results for rats and for pigeons when session length varied suggest that at least one of the factors that produces the within-session changes in responding is shared by the present species, responses, and reinforcers. The differences in results when rate of reinforcement varied are more difficult to interpret. 相似文献
13.
The degree of stereotypy in the movement patterns of 3 pigeons during noncontingent and contingent periodic food reinforcement was quantified by analyzing the distribution of turning angles, and by using information and Fourier analyses. The results indicated that (1) movement patterns were less stereotyped during noncontingent than during contingent reinforcement, (2) a reversal to noncontingent reinforcement resulted in a degree of stereotypy comparable to that during the first phase of noncontingent reinforcement, (3) movement patterns were maximally stereotyped immediately after food withdrawal and generally became less stereotyped as reinforcement approached, regardless of whether reinforcement was noncontingent or contingent, and (4) higher frequency movements generally accounted for more variance in the movements during contingent than during noncontingent reinforcement. Greater stereotypy in the movements during contingent reinforcement was likely due to a greater probability that similar movements were reinforced during contingent reinforcement. Momentary changes in the stereotypy of the movements within the interfood interval might reflect changes in the level of arousal. 相似文献
14.
James D. Dougan Valeri A. Farmer-Dougan Frances K. McSweeney 《Learning & behavior》1989,17(2):247-255
The effects of reinforcement rate on behavioral contrast were examined in pigeons and rats. Each species was exposed to a series of 12 multiple variable-interval schedules, divided into four 3-schedule series. Each series consisted of a standard contrast manipulation, and baseline schedules provided a different rate of reinforcement in each of the series. The functions relating reinforcement rate to the magnitude of contrast were different across species. Rats showed a U-shaped function, with reliable contrast occurring only at high reinforcement rates. Pigeons showed an inverted U-shaped function, with contrast occurring on all schedules except the schedule providing the lowest rate of reinforcement. Pigeons discriminated between schedule components better than rats did, although differences in discrimination were probably not responsible for the differences in contrast. The results suggest that behavioral contrast in rats may be a different phenomenon from behavioral contrast in pigeons. The results cannot be explained by current theories, which view contrast as the product of a single general process. 相似文献
15.
In Experiment 1, pigeons were trained to peck red or blue keys for food reinforcement at variable intervals, while food was contingent on withholding key pecks in the presence of a vertical line (omission training). When the line was briefly superimposed on red or blue in a compound test, responding was reduced. When the orientation of the line was varied during extinction, generalization gradients were variable but often had most responding at or near vertical. In Experiment 2, pigeons were trained in a discrete trials procedure that made food contingent upon pecking in the presence of triangle, and upon the absence of pecking in the presence of red (omission training). Food was never given on green-key trials (extinction). When red or green backgrounds were presented with the triangle in a compound test, responding was reduced similarly in the presence of both key colors. Subsequent resistance to auto-shaping was also similar for red and green. These data, taken together with reports in the literature, suggest that the inhibitory effects of omission training are quite similar to those of extinction. Thus, the crucial condition for obtaining inhibitory effects is not a negative stimulus-reinforcer correlation, as in extinction, but simply the establishment of low rates of responding to the inhibitory stimulus. 相似文献
16.
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
17.
Frances K. McSweeney 《Learning & behavior》1978,6(4):444-450
Four pigeons pecked keys and pressed treadles for food reinforcers delivered by several variable-interval schedules of reinforcement. Then the subjects responded on several concurrent schedules. Keypecking produced reinforcers in one component, and treadle-pressing produced reinforcers in the other. The changeover delay, which prevented reinforcement after all switches from one response to the other, was 0, 5, or 20 sec long. An equation proposed by Kerrnstein (1970) described the rates of treadle-pressing and keypecking emitted during the variable-interval schedules. The k parameter of this equation was larger for keypecking than for treadle-pressing. The R0 parameters were not systematically different for the two responses. The rates of keypecking and treadle-pressing emitted during the components of the concurrent schedules correlated with, but were not equal to, the rates of responding predicted by Herrnstein’s equation and the subject’s simple schedule responding. The ratios of the rates of responding emitted during, and the ratios of the time spent responding on, the components of the concurrent schedules conformed to an equation proposed by Baum (1974), but not to Herrnstein’s equation. 相似文献
18.
Five groups of pigeons were studied in an auto-shaping procedure which programmed two types of trials represented by hues on the response key. Each signal was separated by a brief intertriai interval. Three groups were studied with a positive correlation between one of the signals and food (contingent groups). They differed with respect to the frequency with which the positive signal appeared. Two noncontingent groups were studied in which the correlation between the signals and food was eliminated by programming food with the same probability following either signal. One noncontingent group had a high density of reinforcement produced by adding reinforcement in the other signal, at the same rate as programmed in the positive signal for the contingent groups. The other noncontingent group experienced the same number of reinforcements in the session as the contingent group with the least frequent positive trial, but these reinforcements were distributed with equal probability across the signals. Birds in the contingent groups with intermediate or infrequent positive signals all acquired reliable pecking, with acquisition most rapid for the infrequent signal. Maintained responding covaried with the speed of acquisition. No birds in the noncontingent groups showed reliable responding. Birds in the contingent group with a frequent positive signal (approximately 3/4 of the session), also showed no reliable pecking. This result suggests that more than one noncontingent group is informative for assessing the role of differential reinforcement probability in the acquisition of auto-shaped keypecking. In particular, a noncontingent group which controls for the frequency of reinforced trials is an appropriate reference group.
相似文献19.
Each of four pigeons was exposed to a single random-ratio schedule of reinforcement in which the probability of reinforcement
for a peck on either of two keys was 1/25. Reinforcer amounts were determined by an iterated prisoner’s dilemma (IPD) matrix
in which the “other player” (a computer) playedtit-for-tat. One key served as thecooperation(C) key; the other served as thedefection(D) key. If a peck was scheduled to be reinforced and the D-key was pecked, the immediate reinforcer of that peck was always
higher than it would have been had the C-key been pecked. However, if the C-key was pecked and thefollowing peck was scheduled to be reinforced, reinforcement amount for pecks on either key were higher than they would have been if
the previous peck had been on the D-key. Although immediate reinforcement was always higher for D-pecks, the overall reinforcement
rate increased linearly with the proportion of C-pecks. C-pecks thus constituted a form of self-control. All the pigeons initially
defected with this procedure. However, when feedback signals were introduced that indicated which key had last been pecked,cooperation (relative rate of C-pecks)—hence, self-control—increased for all the pigeons. 相似文献
20.
Louis D. Matzel 《Learning & behavior》1985,13(2):187-193
A series of experiments used food-deprived pigeons to examine several parameters of reinforcement omission in an attempt to control changes of keypeck response measures on a subsequent schedule. In Experiments 1 and 2, the pigeons were tested with a multiple fixed-ratio schedule on which reinforcement was occasionally omitted at the completion of the first component. The duration of the delay occurring in lieu of reinforcement was systematically varied. In Experiment 3, the stimulus that signaled the second component of the schedule was altered to appear either more or less similar to the stimulus that signaled the first component. Two principal results are reported: (1) Response latency decreased and, to a much lesser extent, terminal response rate increased as the delay occurring in lieu of reinforcement decreased; and (2) both latency decrease and response-rate increase were enhanced by a second component stimulus which was similar to the first. The results are evaluated in terms of Amsel’s frustration theory and an analysis by Staddon which suggests that reinforcement inhibits responding. The data appear to support Staddon’s argument that rate increases and latency decreases following reinforcement omission are largely a function of an attenuation of the inhibitory influence of reinforcement, an effect that is enhanced by stimulus generalization. Accordingly, it is proposed that an animal’s response to reinforcement omission is determined by a stimulus complex that minimally includes the omission event and component cues. 相似文献