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1.
Although considerable attention has been given to interactions between events serving as the positive (S+) and negative (S−) stimuli in successive discriminations, there has been little study of similar interactions in simultaneous discriminations. We propose that in a simultaneous discrimination, given what is typically relatively little experience with the consequences of responding to the S−, some of the value of the S+ transfers to the S− with which it was paired. Furthermore, the mechanisms responsible for this transfer of value appear to be the higher order Pavlovian association between the S− and the S+, as well as within-event associations between them. Although in typical simultaneous discriminations, negative value does not appear to transfer from the S− to the S+, when adequate experience is provided with the S−, contrast typically develops, reducing the value of the S− (negative contrast) and enhancing the value of the S+ (positive contrast). This model of stimulus interactions has implications not only for simple simultaneous discrimination learning, but also for research using combinations of discriminations (e.g., transitive inference in animals and humans). This model may also have implications for a number of human social psychological phenomena. 相似文献
2.
In a simultaneous discrimination involving a positive (S+) and a negative (S−) stimulus, positive value appears to transfer from the S+ to the S−. However, negative value does not appear to transfer from the S− to the S+. Instead, when sufficient experience with the contingencies associated with responding to the S− is provided, it appears that the presence of the S− enhances the value of the S+ (i.e., a contrast effect is found). The purpose of the present experiments was to further examine the influence of the S+ on the S− in a simultaneous discrimination (between subjects in Experiment 1 and within subjects in Experiment 2). In both experiments, we found that under typical training conditions, given little direct experience with the value of the S−, value transfers from the S+ to the S−. If sufficient experience with the value of the S− is provided, however, contrast between the S+ and the S− can be demonstrated. Thus, in a simultaneous discrimination, value transfer from the S+ to the S− depends on the animal’s having responded relatively little to the S−. 相似文献
3.
When pigeons are trained on a discrete-trial simultaneous discrimination, some of the value associated with the positive stimulus appears to transfer to the negative stimulus (Zentall & Sherburne, 1994). Pigeons preferred a negative stimulus that had been discriminated from an always-positive stimulus (S+) over a negative stimulus that had been discriminated from a sometimes-positive stimulus (S±). A very different finding (suggestive of transitivity of preference or contrast) was reported by Belke (1992). On concurrent probe tests of stimuli associated with equal variable interval (VI) schedules but originally trained in alternative concurrent pairs (one with a richer schedule, the other with a poorer schedule—VI 20 sec vs. VI 40 sec and VI 40 sec vs. VI 80 sec), the stimulus originally paired with the poorer schedule was preferred. But Belke’s results may have been obtained because the pigeons had been trained to peck the VI 40 sec paired with the poorer schedule and they had been trained not to peck the VI 40 sec paired with the richer schedule. In the present experiment, we avoided this bias by training pigeons on two concurrent schedules in which the tested stimuli both had been associated with the poorer schedule of the pair [A(VI 20 sec) vs. B(VI 80 sec) and C(VI 40 sec) vs. D(VI 80 sec)]. Evidence for value transfer was demonstrated when on probe trials pigeons preferred B over D. 相似文献
4.
These experiments examined one way in which the allocation of attentional resources can change performance during a visual discrimination task. Pigeons were trained to discriminate visual forms under conditions that produced dimensional contrast. In three experiments, negative training stimuli differed from positive stimuli either along a primary physical dimension alone or along both a primary dimension and an orthogonal dimension. When a negative stimulus differed from positive stimuli along two dimensions, discrimination of that negative stimulus improved. For one type of visual form, discrimination of the positive stimuli declined with orthogonal variation in a negative stimulus, whereas for other visual forms, there was no decline in performance. These results are consistent with a model of dimensional contrast that suggests that differences in the allocation of attentional resources determine discrimination performance. The results also indicate that the organization of stimulus dimensions plays a crucial role in the allocation of attentional resources in these settings. 相似文献
5.
Prior research on Pavlovian-to-instrumental transfer has shown that when a CS previously associated with shock (AvCS+) is presented contingent upon a choice response to a discriminative stimulus for food reinforcement, it facilitates discrimination learning. Conversely, a response-contingent CS previously associated with the absence of shock (AvCS?) retards discrimination learning. To evaluate whether these findings reflect across-reinforcement blocking and enhancement effects, two experiments investigated the effects of appetitively conditioned stimuli on fear conditioning to a novel stimulus that was serially compounded with the appetitive CS during conditioned-emotional-response (CER) training. Although there were no differential effects of the appetitive CSs in CER acquisition, Experiment 1, using a relatively weak shock US, showed that a CS previously associated with food (ApCS+) retarded CER extinction to the novel stimulus, in evidence of enhanced fear conditioning to that stimulus. In addition, Experiment 2, using a stronger shock US, showed that a CS previously associated with the absence of food (ApCS?) facilitated CER extinction to the novel stimulus, in evidence of weaker fear conditioning to that stimulus. These results parallel traditional blocking effects and indicate not only that an ApCS+ and an ApCS? are functionally similar to AvCSs of opposite sign, but that their functional similarity is mediated by common central emotional states. 相似文献
6.
Patricia B. Cronin 《Learning & behavior》1980,8(3):352-358
Delayed-reward learning in pigeons was examined using a simultaneous red-green visual discrimination task in which the conditions during the delay interval were varied between groups. The nondifferential group received training in which the stimulus present during the 1-min delay was the same following a peck on the correct and incorrect colors. The other three groups received 1-min delay training in which different stimuli occurred in the delay interval following correct and incorrect choices. The differential group received continuous, differential stimuli during the delay. The reinstatement group received the differential stimuli in the 10 sec immediately following the choice and during the last 10 sec of the delay. The reversedcue group was treated in the same way, except that the 10-sec delay stimulus immediately following an incorrect response was also presented for 10 sec prior to reward on correct choices, and the stimulus following a correct response also occurred 10 sec before nonreward on incorrect choices. Nondifferential birds failed to learn the discrimination, while differential and reinstatement birds learned it readily. The reversed-cue birds learned to choose the incorrect stimulus. Differential and reinstatement birds showed no decrement in performance when the delay was increased to 2 min. These findings suggest that similarity of prereward and postresponse delay stimuli controls choice responding in long-delay learning, a finding compatible with both memorial and conditioned reinforcement interpretations. 相似文献
7.
The similarity in the discrimination training leading to behavioral contrast and that preceding tests producing response enhancement to combined discriminative stimuli suggested that the two phenomena might be related. This was investigated by determining if contrast indiscrimination training was necessary for this outcome of stimulus compounding. Responding to tone, light, and to the simultaneous absence of tone and light (T + L) was maintained during baseline training by food reinforcement in Experiment I and by shock avoidance in Experiment II. During subsequent discrimination training, responding was reduced in T + L by programming nonreinforcement in Experiment I and safety or response-punishment in Experiment II. In the first experiment, one rat exhibited positive behavioral contrast, i.e., tone and light rates increased while his T + L rate decreased. In Experiment II, rats punished in T + L showed contrast in tone and light, this being the first demonstration of punishment contrast on an avoidance baseline with rats. The discrimination acquisition data are discussed in the light of current explanations of contrast by Gamzu and Schwartz (1973) and Terrace (1972). During stimulus compounding tests, all subjects in both experiments emitted more responses to tone-plus-light than to tone or light (additive summation). An analysis of the terminal training baselines suggests that the factors producing these test results seem unrelated to whether or not contrast occurred during discrimination training. It was concluded that the stimulus compounding test reveals the operation of the terminal baseline response associations and reinforcement associations conditioned on these multicomponent free-operant schedules of reinforcement.
相似文献8.
Stephen C. Brake 《Learning & behavior》1978,6(4):435-443
Rats were given continuous reinforcement (CRF), partial reinforcement (PRF), or successive discrimination (D) training in an alley from 11–14 (Age 1) or 15–18 (Age 2) days of age. Reinforcement was the opportunity to suckle the dry nipples of an anesthetized dam. Following a 10-day interval, all animals were given 4 successive days of discrimination training with food pellets as reinforcement. Control groups were given only the second phase of training. In the first phase, D subjects of both ages responded appropriately to the discriminative stimuli, and the PRF subjects of both ages ran significantly slower than CRF subjects. In the second phase, only the CRF subjects of Age 1 showed behavioral discrimination. All three Age 2 groups discriminated, but the discrimination developed earliest after Phase I CRF and latest after Phase I PRF. Both Age 1 control groups showed a late-developing discrimination, but neither Age 2 control group discriminated. The results suggest that infant and preweanling rats can learn both positive and negative expectancies of appetitive events, respond appropriately, and retain and transfer these expectancies to new learning. The reinforcement value of dry suckling and the effects of stimulus preexposure in infant rats are also discussed. 相似文献
9.
Charles Lawrence 《Learning & behavior》1973,1(1):60-64
Two groups of four pigeons each were trained on a discrimination between two intensities of white noise. The low-intensity group had a 60-dB intensity as the negative discriminative stimulus (S?) and a 70-dB intensity as the positive discriminative stimulus (S+): the high-intensity group had a 95-dB intensity as S? and an 85-dB intensity as S+. Generalization stimuli were all of higher intensity than S+ for the former group and all of lower intensity than S+ for the latter group. The rate of acquisition of the discrimination was faster for the Ss in the high-intensity group. In both groups, the maximum of the generalization function was shifted toward the middle values of the set of test stimuli, away from the training stimuli. Responding showed a decline at the far end of the range of test stimuli. Responding to the positive training stimulus was initially as great as it had been on the preceding training sessions, but became markedly depressed relative to responding to the other stimuli as the test progressed. 相似文献
10.
The monkey’s capacity to extract tonal pattern from a sequence of tones was assessed in four subjects that had the benefit of substantial past experience in discriminating, matching, and remembering acoustic stimuli. In Experiment 1, the monkeys failed to transfer their well-established matching behavior to the matching of two structured sequences of tones that differed primarily in tonal pattern, indicating that for them tonal pattern was not a salient feature of the acoustic stimuli. Experiment 2 was an attempt to encourage tonal pattern perception by employing, within a discrimination paradigm, very simple tonal patterns and multiple exemplars of the positive and negative patterns; the transfer design, borrowed from Hulse and Cynx (1985), was a powerful one for revealing tonal pattern perception. Verifying earlier results from our laboratory, there was little in the monkeys’ transfer performance to indicate that they had extracted tonal pattern from the acoustic stimuli. Major discriminative control seemed to be vested in the first tone of each exemplar. This apparent cognitive limitation may be rather general among animals, perhaps reflecting an intimate connection between the capacity for tonal pattern perception and that for acoustically based language. 相似文献
11.
Pigeons received variable-interval (VI) reinforcement for keypecking during randomized presentations of seven line-orientation stimuli forming a continuum ranging from horizontal (0 deg) to vertical (90 deg). Each line presentation lasted for 30 sec and was preceded and followed by 30-sec time-outs. After responding stabilized, only responding in the two extreme stimuli (0 and 90 deg) was reinforced. As discrimination training proceeded, strong behavioral contrast and dimensional contrast effects appeared. However, only marginal local effects (local contrast and local dimensional effects), exerted by one line-orientation component upon a second, appeared, indicating that behavioral and dimensional contrast may be independent of parallel local effects. An attempt was made to apply Blough’s (1975) quantitative model of operant generalization and discrimination to the present discrimination procedure. However, this model did not predict the generalization gradient shape that was experimentally obtained. This experiment also yielded two serendipitous findings: (1) Positive behavioral contrast appeared in an extinction-related stimulus (time-out) when other stimuli were switched from reinforcement to extinction (hitherto, positive behavioral contrast had been observed only in responding to a reinforcementrelated stimulus when other stimuli were switched from reinforcement to extinction), and (2) final responding was higher in the presence of an extinction stimulus that had always been an extinction stimulus than it was in the presence of other extinction stimuli that had previously been paired with VI reinforcement. 相似文献
12.
Prior research indicated that a training sequence consisting of a negative stimulus followed by a positive stimulus constitutes the minimal condition for the production of postdiscrimination phenomena typically observed after training with random sequences of the discriminanda. The present experiments, employing multiple schedules with pigeon subjects, confirmed the earlier findings but indicated that they are restricted to procedures in which the reinforcing stimulus may acquire a discriminative function that competes with the control exerted by the nominal discriminanda. The sequences in which the discriminanda were presented did not differentially affect subsequent measures of generalization and transfer if the discriminative function of reinforcement were degraded either by introducing some reinforcers during the negative stimulus (Experiment 1) or by omitting some reinforcers during the positive stimulus (Experiment 2). It was concluded that the sequence in which the discriminanda are presented during discrimination training does not contribute fundamentally to the processes responsible for discrimination formation with random training sequences. 相似文献
13.
Blough DS 《Learning & behavior》2004,32(2):157-172
In three experiments with pigeons, the similarity of unreinforced test stimuli to a reinforced stimulus and the frequency
of reinforcement associated with a stimulus were varied. The stimulus on each trial was a small spot that appeared in different
hues or, in Experiment 3, different forms. Differential response frequency and reaction time (RT) patterns emerged: Changes
in similarity affected the percentage of stimuli responded to but left the shape of RT distributions about the same, whereas
changes in reinforcement shifted RT distributions but had little effect on the percentage of responses. When the similarity
and reinforcement variables were applied to the same stimuli (Experiment 2), their effects were largely independent. A generalization
procedure (Experiment 3) replicated the similarity effects of the initial discrimination procedure. The RT distributions were
modeled by a diffusion process, and implications for a memory-instance model were suggested. 相似文献
14.
Pigeons were given successive discrimination training in which pecking during a choice period when the key was white was either reinforced or not, depending upon the prior presence or absence of a discriminative stimulus, which was a two-element serial compound. The compound consisted of a keylight and food, with food presented second or first in a forward or backward pairing for different groups of pigeons. In Experiment 1, the sequence was an S+ indicating reinforced trials, while in Experiment 2, the sequence was an S? indicating nonreinforced trials. Following acquisition of discriminated operant behavior, a sequence generalization test was administered during which all possible orders of the two stimuli were presented on test trials prior to the onset of the choice period. The results showed that food overshadowed stimulus control by the color of the light on the key on the sequence-generalization test, independently of whether food was presented first or second during training and independently of whether food was associated with reinforcement or nonreinforcement. The similarity of results for the two experiments suggests that overshadowing occurs independently of whether the compound is a discriminative stimulus for reinforcement or nonreinforcement. Simultaneous presentation of elements of a compound stimulus is not necessary for overshadowing because the phenomenon was captured with sequentially presented stimuli. 相似文献
15.
An attempt was madeto manipulate the strength of internal stimulus representations by exposing pigeons to brief delays between sample offset and comparison onset in a delayed conditional discrimination. In Experiment 1, pigeons were first trained on delayed conditional discrimination with either short (0.5-sec) delays or no delays. When delays were increased by 2.0 sec, birds trained with a delay performed at a higher level than did birds trained with no delays. In Experiment 2, subjects were first trained on a delayed simple discrimination. Following a circle stimulus, responses to a white key were reinforced; however, following a dot stimulus, responses to the white key were not reinforced. The pigeons were then trained on a delayed conditional discrimination involving hue samples and line-orientation comparisons with differential outcomes. Choice of vertical following red yielded food; choice of horizontal following green yielded no food. Mixed delays were then introduced to birds in Group Delay, whereas birds in the control group received overtraining. When tested on a delayed simple discrimination with hue stimuli (red and green initial stimuli followed by white response stimulus), pigeons in Group Delay tended to perform at a higher level than did birds in the control group (i.e., although the birds in both groups responded more following red than following green, birds in Group Delay did this to a greater extent than did birds in the control group). Thus, experience with delays appears to strengthen stimulus representations established during training. 相似文献
16.
Minimal procedures for the demonstration of transitive inference (TI) in animals have involved the training of four simultaneous discriminations: for example, A+B?, B+C?, C+D?, and D+E?, followed by the demonstration of a preference for B over D on test trials. In Experiment 1, we found that TI in pigeons can be found with successive training involving A+B?, B+C?, A+C?, C+D?, D+E?, C+E?, and A+E?. In Experiment 2, we found that demonstration of TI did not require inclusion of experience with the nonadjacent stimulus pairs (A+C?, C+E?, A+E?). Experiment 3 provided a test of value transfer theory (VTT; Fersen, Wynne, Delius, & Staddon, 1991). When pigeons were trained with stimulus pairs that did not permit the transitive ordering of stimuli, but did permit the differential transfer of value (e.g., A+B?, C?E+, C+D?, & A+E?), preference for B over D was still found. Analyses of the relation between direct experiences with reinforced and nonreinforced responding and stimulus preferences on test trials failed to support a reinforcement-history account of TI. 相似文献
17.
Young adult subjects were trained in a discrimination involving three pure tones varying in pitch, with two positive stimuli and a negative stimulus located midway between the two. Subjects in the control conditions were trained only with the two positive stimuli. Generalization gradients were bimodal in all cases, but for the control subjects, the modes were at the positive stimulus values, while postdiscrimination gradients were displaced away from the negative stimulus toward the extremes of the continuum. Since, with this procedure, the training and test adaptation levels were the same, the observed displacements are difficult to explain in terms of an adaptation-level account of peak shifts. The observed shifts are more consistent with the conditioning-extinction model which assumes interactions between inhibitory and excitatory gradients. However, overall response rates did not reflect the action of summation processes. 相似文献
18.
Two experiments were conducted to determine if contextual stimuli used as S2 in a higher-order differential conditioning procedure would control the performance of rats. Discrete stimuli were first paired with footshock in a separate training context. During second-order training, a shock-associated discrete stimulus was presented in one of two discriminable observation chambers. Over 4 days of training, subjects engaged in more freezing in the context associated with an excitatory discrete S1, relative to a context in which no discrete stimulus, or a stimulus that had been explicitly unpaired with shock delivery, was presented. After acquisition of the second-order discrimination, animals were returned to the original training context where they received a “signaled inflation” treatment designed to change the current value of S1, and the US. This postconditioning manipulation did not selectively affect performance of defensive freezing or conditional analgesia in S2. 相似文献
19.
We report the first successful demonstration of a simultaneous, two-itemsame-different (S/D) discrimination by 6 pigeons, in which nonpictorial color and shape stimuli were used. This study was conducted because
the majority of recently successful demonstrations of S/D discrimination in pigeons have employed displays with more than
two items. Two pairs of stimulus items were simultaneously presented on a touch screen equipped computer monitor. Pigeons
were reinforced for consistently pecking at either thesame (i.e., identical) or thedifferent (i.e., nonidentical) pair of items. These pairs were created from combinations of simple colored shapes drawn from a pool
of six colors and six shapes. After acquiring the discrimination with item pairs that differed redundantly in both the shape
and the color dimensions, the pigeons were tested for transfer to items that varied in only one of these dimensions. Although
both dimensions contributed to the discrimination, greater control was exhibited by the color dimension. Most important, the
discrimination transferred in tests with novel colored, shaped, and sized items, suggesting that the mechanisms involved were
not stimulus specific but were more generalized in nature. These results suggest that the capacity to judge S/D relations
is present in pigeons even when only two stimuli are used to implement this contrast. 相似文献
20.
Three experiments on classical differential conditioning of the human skin conductance response to elemental and compound stimuli are reported. Subjects in Experiment 1 received both positive and negative patterning training, followed by either positive or negative patterning transfer tests on new stimuli. In positive patterning, a compound of two stimuli is reinforced and its elements are nonreinforced. In negative patterning, the elements are reinforced and the compound is nonreinforced. Subjects in Experiments 2 and 3 received either positive or negative patterning during training, followed by transfer tests on new stimuli. In Experiment 2, the transfer series began with new elements, after which their compound was presented; in Experiment 3, the new compound was presented first in the transfer series, and then the separate elements were administered. All three experiments provided evidence of the acquisition of positive patterning, while negative patterning was found only in Experiments 2 and 3. Positive patterning transferred to new stimuli, indicating that it was not attributable solely to summation of sub-threshold excitation conditioned to the elements on reinforced compound trials. This finding, coupled with the negative patterning found in Experiments 2 and 3, provided support for the unique cue hypothesis. It was concluded that the assumed unique cue constituted a learned “rule,” and that the actual elemental stimuli were neither perceptually nor otherwise modified during the conditioning process. 相似文献