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1.
In three experiments, rats were trained to discriminate between 20 and five (Exps. 1 and 2), or between 40 and five (Exp. 3), black squares. The squares were randomly distributed in the center of a white background and displayed on a computer screen. For one group, the patterns containing the higher quantity of squares signaled the delivery of sucrose (+), whilst patterns with the lower quantity of squares did not (–). For the second group, sucrose was signaled by the lower, but not by the higher, quantity of squares. In Experiment 1, the intertrial interval (ITI) was a white screen, and the 20+/5– discrimination was acquired more readily than the 5+/20– discrimination. For Experiment 2, the ITI was made up of 80 black squares on a white background. In this instance, the 5+/20– discrimination was acquired more successfully than the 20+/5– discrimination. In Experiment 3, two groups were trained with a 40+/5– discrimination, and two with a 5+/40– discrimination. For one group from each of these pairs, the training trials were separated by a white ITI, and the 40+/5– discrimination was acquired more readily than the 5+/40– discrimination. For the remaining two groups, the training trials were not separated by an ITI, and the two groups acquired the task at approximately the same rate. The results indicate that the cues present during the ITI play a role in the asymmetrical acquisition of magnitude discriminations based on quantity.  相似文献   

2.
Four experiments were performed to determine the stimulus characteristics that favor the development of conditional stimulus control in the single reversal paradigm with pigeon subjects. In Experiment 1, pigeons were trained on a successive discrimination between tone frequencies ranging from 350 to 3500 Hz in a particular houselight context condition (houselight-on or -off). The subjects then were trained on the reversal of the tone discrimination in the alternative context. Subsequent tone-frequency generalization testing in the two contexts indicated that they had failed to gain conditional control over the pigeons’ discriminative performance. Such control was obtained in Experiment 2, in which the two problems were alternated daily for 32 sessions of training. The gradients then peaked at the appropriate S+ value in each context. In Experiment 3, the key colors (blue vs. red) served as contexts while pigeons learned a successive discrimination in which the discriminative cues were houselight-on versus houselight-off conditions. This was followed by a reversal of the discrimination in the alternative key-color context condition. The key colors were effective conditional cues in this situation. In a previous experiment (Thomas, McKelvie, & Mah, 1985), key color had been ineffective as a conditional cue when the discriminative cues were lines superimposed on the colored background. In Experiment 4, key color was effective when the color and lines were presented on a single key as in the earlier experiment, but were sequenced such that the onset of the key color preceded and then overlapped the presentation of the lines. We concluded that conditional discriminations are easiest for pigeons when visual cues are used, but the conditional and discriminative cues must be presented in such a way that they do not combine to form a psychological compound.  相似文献   

3.
In two experiments, participants acquired one of two target configural discriminations (a biconditional or negative patterning discrimination) in a predictive learning task. In Experiment 1, participants were pretrained with either a configural or an elemental discrimination; in Experiment 2, they were pretrained with a configural discrimination, an elemental discrimination, or a control discrimination that was not expected to bias them toward elemental or configural processing. In both experiments, acquisition of the target configural discriminations was faster after configural pretraining than after elemental pretraining. In addition, the negative patterning discrimination was acquired faster than the biconditional discrimination. Finally, the results of Experiment 2 were more consistent with the notion that elemental pretraining hindered acquisition of the target discriminations than with the notion that configural pretraining enhanced their acquisition. Implications of these findings are discussed.  相似文献   

4.
In Experiment I, one group of goldfish (TD) was trained to discriminate blue and green while a second group (PD) was exposed to the same colors in a “pseudodiscrimination,” after which both groups were reinforced for response to a tone. The TD group subsequently showed a sharper auditory discrimination gradient than the PD group and performed better in a differentially reinforced tone discrimination. The former PD animals then were given true discrimination training and the former TD animals pseudodiscrimination training with the colors, after which the first group showed better tone discrimination than the second. These results are analogous to those found in pigeons and rats. In Experiment II, goldfish which were trained in an easy color discrimination and shifted to a more difficult tone discrimination performed better than a control group trained from the outset with the tones. This result suggests that the dimensional specificity of the processes responsible for “transfer along a continuum” cannot safely be assumed in the absence of appropriate controls.  相似文献   

5.
Resistance to interference was examined in rats that received a complex negative patterning discrimination in which XA and XB were followed by food reinforcement and XAB was not. Retention of the discrimination was evident after separate reinforcement of both A and B (Experiment 3), but not after reinforcement of either AB (Experiments 1 and 3) or XAB (Experiments 2 and 3). These data suggest that complex negative patterning discriminations are acquired configurally and that the relative similarity of the original discrimination and subsequent interference trials dictates the final degree of retention observed.  相似文献   

6.
Using trial-and-error training, eight pigeons did not learn to discriminate between 45° and 135° lines, but did learn to discriminate between red and green colors. Control by line tilt was induced by stimulus fading that did not include reinforcement while fading out the colors. After establishing the red–green discrimination, low-intensity lines were superimposed on colors and were gradually faded in. All of this was done using reinforcement. At the end of the line fade-in, the lines had not acquired control of responding. Finally, color intensity was gradually faded out in the absence of reinforcement, and the lines acquired discriminative control by six of the eight pigeons. Thus, reinforcement during the color fade-out was not necessary for the acquisition of discriminative control by the lines during fading. Acquisition of control by lines was attributed to overshadowing, the reduction of stimulus blocking by generalization, and the evocation of correct responding by the colors while the participants were attending to the lines. This last process was also responsible for the induction of discriminative control during sensory preconditioning, higher order conditioning, and response transfer in equivalence classes. Errors, however, were not correlated with discrimination learning during stimulus fading. Finally, transfer of control occurred very quickly with or without errors.  相似文献   

7.
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   

8.
Six experiments on learning in honeybees were prompted by the possibility that results previously attributed to a difference in amount of reward (20- versus 5-μl drops of sucrose solution presented on colored targets) might be due at least in part to a difference in delay of reward attendant on greater difficulty in locating the 5-μ1 drops. Substantial reduction in the diameter of the targets, which was designed to facilitate location of the drops, impaired discrimination of the colors, perhaps because their salience was reduced in the process (Experiment 3). White dots used to mark the location of the drops on larger targets also impaired discrimination of the colors, which presumably were overshadowed by the dots (Experiments 1, 2, and 4). That the dots did not serve merely to equate delay but were themselves discriminated was demonstrated in Experiment 5, which produced as well the first indication of an effect of amount of reward uncontaminated by the possibility of differential delay: Animals trained with a 5-μl drop on a dotted target of one color and a drop of the same size on an undotted target of a second color preferred the dotted target, but animals trained with a 5-μl drop on a dotted target of one color and a 20-μl drop on an undotted target of a second color preferred the undotted target. In Experiment 6, with odors substituted for the colors on the assumption that they were less likely to be overshadowed by the dots, what could be interpreted as a pure amount effect was found again. Aside from their relevance to questions about the role of amount of reward, the results have some interesting implications for the theory of discriminative learning in honeybees.  相似文献   

9.
Honeybees were trained to discriminate between simultaneously presented color-odor compounds, one group with color and odor confounded and a control group with color relevant and odor irrelevant; in subsequent differentially reinforced training with the colors in the absence of the odors, the performance of the two groups was the same (Experiment 1). When, however, response to the colors was measured in a 10-min extinction test, discrimination was found to be poorer after confounded training (Experiment 2), and like results were obtained in an extinction test with the odors after control animals had been trained with odor relevant and color irrelevant, the confounded animals showing poorer discrimination of the odors than the controls (Experiment 3). The results of the first two experiments, in which overshadowing of color by odor was found only with an extinction test, require us to take seriously the possibility that our previous modeling experiments (with probability of correct choice in differentially reinforced training as the measure of performance) may have been insufficiently sensitive to noncontinuity effects. Our first efforts to model extinction suggest, however, that all the results of the present experiments can be understood without sacrifice of the parsimonious independence principle.  相似文献   

10.
In three experiments, we examined how matching-to-sample by pigeons is affected by discrimination versus nondifferential training between the matching stimuli. In Experiment 1A, pigeons responding differentially to the sample stimuli off-baseline acquired accurate matching performances more rapidly than did pigeons responding nondifferentially to those same stimuli. In Experiment 1B, tests involving reversal of the off-baseline requirements demonstrated that the birds were primarily controlled in their matching choices by the sample stimuli. The results of Experiment 2 showed that off-baseline nondifferential training did not retard acquisition relative to comparable training between stimuli unrelated to the matching task. Together, these results suggest that discrimination training can facilitate matching acquisition by enhancing attention to the sample stimuli.  相似文献   

11.
Goldfish, trained in the avoidance shuttlebox with a variant of the linear discrimination procedure, learned to conditionally discriminate between color signals, both for the matching (M) and oddity (O) criterion forms. Transfer to assess the possibility of concept learning was also tested. In original learning, oddity-trained groups learned faster and reached higher conditional discrimination performance levels than did matching-trained groups. In transfer, various groups were tested with the same criterion (MM or OO) or a shifted criterion (MO or OM), and half of each group retained the same color signals and the remaining half had its color signals changed in transfer. Groups with the same criterion in original learning and transfer (MM or OO), regardless of signal colors, showed comparable positive transfer. Groups with their criterion shifted between original learning and transfer (MO or OM) showed comparable negative transfer, regardless of signal colors. Since both positive- and negative-transfer effects were independent of signal colors, it is clear that what was learned for one set of signal colors transferred to at least one other signal-color set. These findings are consistent with the interpretation that goldfish learned the original conditional discrimination at a conceptual level, and learned about the general matching or oddity relationships between colors, rather than about a specific set of colors.  相似文献   

12.
Willson and Wilkie (1993) developed a novel procedure for assessing pigeons’ memory for the spatial location of food. Only one of four locations (consisting of an illuminated pecking key and grain feeder) provided food each day. Over days, different locations provided food. The pigeons’ tendency to revisit the location that was profitable on the previous day demonstrated memory for food-spatiallocation associations over a period of 24 h, retention longer than previously reported for this species. This basic finding was replicated and extended in three experiments. Experiment 1 demonstrated that location-food discriminations were also remembered well when established with successive rather than concurrent procedures. Experiment 2 demonstrated that pigeons can remember two location-food associations over 24 h. Experiment 3 showed that the discrimination training inherent in this paradigm is important for retention; retention was impaired when only the rewarded location was presented. Overall, this research suggests that cross-species differences in spatial memory performance may be due to quantitative rather than qualitative differences in the memory system underlying performance.  相似文献   

13.
Four colors (red, yellow, green, and blue) were arranged in all possible two-color sets to determine if goldfish can discriminate between color sets associated with shock and color sets associated with safety/shock omission in a one-phase (linear presentation) discrimination-learning procedure. The results showed that goldfish learned to discriminate between two-color sets if set colors were natural categorical color-code mates (red = yellow and green = blue). When natural code mates were not in the same set, and therefore were paired with different shock consequents, no discrimination learning occurred, suggesting that goldfish, unlike pigeons, are not able to code colors arbitrarily. The method also allowed a measure of preference between colors within sets associated with safety/shock omission. Original-learning preference measures between colors in sets so associated showed that goldfish chose red over any other color, yellow over blue or green, and green over blue, despite the fact that both colors in any set were procedurally identical, implying that goldfish do discriminate between colors in the absence of explicit discrimination training. The goldfish that failed to discriminate between red/blue and green/yellow sets in original learning were transferred to red/yellow and blue/green color sets. In transfer, the color paired with safety/shock omission in original learning was preferred over the color paired with shock in original learning, which resulted in a reversal of original-learning color preferences for half the goldfish. The transfer color-preference results imply that the goldfish had associated specific colors with specific shock consequents, but the associations were not robust enough to support discrimination learning in the face of categorical color coding.  相似文献   

14.
Herrnstein and Loveland (1964, pp. 549–551) successfully trained pigeons to discriminate pictures showing humans from pictures that did not. In the present study, a go/no-go procedure was employed to replicate and extend their findings, the primary focus of concern being to reevaluate the role of item- and category-specific information. The pigeons readily acquired the discrimination and were also able to generalize to novel instances of the two classes (Experiment 1). Classification of scrambled versions of the stimuli was based on small and local features, rather than on configural and global features (Experiment 2). The presentation of gray-scale stimuli indicated that color was important for classifying novel stimuli and recognizing familiar ones (Experiments 1 and 2). Finally, the control that could possibly be exerted by irrelevant background features was investigated by presenting the pigeons with images of persons contained in former person-absent pictures (Experiment 3). Classification was found to be controlled by both item- and category- specific features, but only in pigeons that were reinforced on person-present pictures was the latter type of information given precedence over the former.  相似文献   

15.
In two experiments, we investigated the impact of odor preexposure treatments on the acquisition of an olfactory discrimination in dogs. In the first experiment, four groups of dogs were each given five days’ odor-exposure treatment prior to discrimination training. Dogs in the exposure group were exposed to anise extract (S+) for 30 min daily. Dogs in the Pavlovian-relevant pairing group received six daily delayed-conditioning trials to the same S+. The Pavlovian-irrelevant pairing group received conditioning trials to almond extract (S'). Dogs in the control group received no pretreatment. All of the dogs were then trained to detect S+ from a background pine odor (an AX-vs.-X discrimination). The Pavlovian-relevant pairing group acquired the odor discrimination significantly faster than all of the other exposure and control groups, and the remaining groups acquired the discrimination at the same rate as the no-exposure control group. In a second experiment, we extended these results to a within-subjects design using an AX-versus-BX discrimination. Six dogs were simultaneously trained on two different odor discriminations, one discrimination in which the S+ was previously Pavlovian conditioned, and one discrimination in which the S+ was novel. All of the dogs learned the odor discrimination with the previously conditioned S+ faster than they learned the novel odor discrimination, replicating the results of Experiment 1, and demonstrating that familiarity in the form of Pavlovian conditioning enhances odor-discrimination training. The potential mechanisms of the facilitated transfer of a Pavlovian conditioned stimulus to discrimination training are discussed.  相似文献   

16.
Pigeons have difficulty learning a standard oddity task involving two colors and three stimulus positions. In Experiment 1, performance on standard noncorrection trials was compared with performance on (1) rerun correction trials in which errors resulted in trial repetition, (2) noncorrection trials with added “negative instance” trials involving presentation of three stimuli, all of which matched, and (3) a combination of correction and added negative instance trials. Results indicated that negative instances, but not correction trials, significantly facilitated oddity performance. In Experiment 2, Phase 1, number of stimulus positions lit (three or five) was factorially manipulated with number of positions on which the odd stimulus could appear (three or five). An increase in number of positions lit, but not number of positions that could be odd, facilitated performance. In Phase 2, birds transferred from trials with five positions lit to four positions lit performed significantly better than controls; but in Phase 3, the same birds did not perform significantly better than controls when transferred to trials with three positions lit. In both experiments, analysis of performance as a function of response position indicated better performance at the end of each display than in the middle. These results, together with the group performance differences in Experiment 2, suggest that oddity learning in pigeons involves a size, or number, discrimination.  相似文献   

17.
In two experiments, rats were trained on a successive go/no-go discrimination problem in the runway in which the positive (S+) and negative (S?) discriminanda were differentiated by the presence or absence of a distinctive feature. The feature in Experiment 1 was a series of flashing lights over the runway. In Experiment 2, the feature was a pretrial reinforcement (Phase 1), or pretrial reinforcement versus pretrial nonreinforcement (Phase 2). The feature signaled S+ trials in feature-positive (FP) groups and S? trials in feature-negative (FN) groups. The original discrimination was reversed in Phase 2 of both experiments. With the exception of the pretrial nonreinforcement groups in Experiment 2, there was an asymmetry in discrimination learning in both phases of both experiments favoring superior discrimination learning by FN subjects over FP subjects, a feature-negative effect. Implications of the results for an information processing account of asymmetries in learning feature discriminations are discussed.  相似文献   

18.
Pigeons were trained on a task in which a red light of durationt 1 was followed by a green light of durationt 2 and then responses to different keys were reinforced according to whether the durations of the stimuli were the same or different. For Experiment 1, duration pairs consisted of all combinations of 1, 2, 4, and 8 sec. In Experiment 2,different-duration pairs included only combinations witht 1 >t 2 and, in addition, 2 subjects with extended training involving lesser-greater duration comparisons were transferred to the same-different task. Two of 3 subjects learned the task in Experiment 1 and analyses suggested that choices were based on specific instances, not on a temporal same-different rule. All 5 birds acquired the discrimination in Experiment 2, where it appeared that choices were controlled by a combination of relative and absolute rules. Accuracy decreased following transfer from a lesser-greater to a same-different discrimination, but performance was above chance on the first transfer session. In both experiments, however, accuracy was below that found in earlier work with lesser-greater comparisons of duration. These findings are discussed in relation to prior research with lesser-greater comparisons of duration and same-different tasks involving nontemporal stimuli.  相似文献   

19.
Pigeons were trained to discriminate the proportion of red to green color in paired stimulus displays. Initially, the stimuli were horizontal bars composed of continuous blocks of color that varied from being all red versus all green to .5 proportions of these two colors. Discrimination accuracy decreased as a function of the disparity in the proportions of the two colors. This relationship was maintained when the stimulus configurations were altered in various ways. Tests with horizontal bars indicated that the pigeons could utilize differences in the lengths (or areas) of one of the colors when choosing between stimuli. They did not rely only on this type of cue to assess proportion disparities but rather on multiple stimulus parameters. Also, the form of the discrimination function suggests that the pigeons distinguished ratio differences, so that Weber’s law applies to this type of discrimination.  相似文献   

20.
We compared acquisition and performance accounts of human contingency learning. After solving a discrimination in Phase 1, in which Cue A predicted the occurrence of the outcome and Cue B predicted its nonoccurrence (A+/B−), a new discrimination (X+/Y−) was superimposed in Phase 2 (AX+/BY−). The participants were finally trained in Phase 3 with the added discrimination, which either maintained the same contingencies as those in Phase 2 (X+/Y−; Experiment 1) or reversed the contingencies (X−/Y+; Experiment 2). According to competitive-learning theories (e.g., Rescorla & Wagner, 1972), there should be no learning of the added discrimination in Phase 2, so that no advantage or disadvantage for this discrimination should be observed in Phase 3. In contrast, performance theories, such as the comparator hypothesis (Miller & Matzel, 1988), contend that learning of the added discrimination in Phase 2 should proceed normally; so, in Phase 3, an advantage for the added discrimination should be observed in Experiment 1, but a disadvantage should be observed in Experiment 2. Our participants learned about the added discrimination and generally showed the effects predicted by the comparator hypothesis.  相似文献   

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