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1.
Goldfish, trained in the shuttlebox apparatus to avoid shock, acquired a color discrimination between two colors (red/green) and were tested in transfer with a new set of colors (yellow/blue). Transfer color shock-pairing was either consistent with (red=yellow, blue=green) or opposite to (red≠ yellow, green≠blue) categorical color coding seen in pigeons. Groups with transfer shock-pairing consistent with categorical color coding showed positive transfer, and groups with transfer shock-pairing opposite to categorical color coding showed negative transfer, similar to an attenuated reversal learning effect. These results indicate that goldfish, like pigeons, code different colors as behavioral equivalents even though they can easily learn to discriminate between them. As with pigeons, the finding of the categorical color coding phenomenon changes the conclusions drawn from earlier goldfish conditional-discrimination transfer studies using only signal color changes between acquisition and transfer testing, from evidence of concept learning to evidence for categorical color coding, on the grounds of parsimony. It is important to note that this finding affects only the explanation of conditional-discrimination transfer effects, and the fact remains that both pigeons and goldfish can learn to conditionally discriminate—pigeons for positive reinforcement, and goldfish to avoid shock.  相似文献   

2.
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   

3.
Two theories of timing, scalar expectancy theory (SET) and learning-to-time (LeT), make substantially different assumptions about what animals learn in temporal tasks. In a test of these assumptions, pigeons learned two temporal discriminations. On Type 1 trials, they learned to choose a red key after a 1-sec signal and a green key after a 4-sec signal; on Type 2 trials, they learned to choose a blue key after a 4-sec signal and a yellow key after either an 8-sec signal (Group 8) or a 16-sec signal (Group 16). Then, the birds were exposed to signals 1 sec, 4 sec, and 16 sec in length and given a choice between novel key combinations (red or green vs. blue or yellow). The choice between the green key and the blue key was of particular significance because both keys were associated with the same 4-sec signal. Whereas SET predicted no effect of the test signal duration on choice, LeT predicted that preference for green would increase monotonically with the length of the signal but would do so faster for Group 8 than for Group 16. The results were consistent with LeT, but not with SET.  相似文献   

4.
In temporal discriminations tasks, more than one stimulus may function as a time marker. We studied two of them in a matching-to-sample task, the sample keylight and the houselight that signaled the intertrial interval (ITI). One group of pigeons learned a symmetrical matching-to-sample task with two samples (2 s or 18 s of a center keylight) and two comparisons (red and green side keys), whereas another group of pigeons learned an asymmetrical matching-to-sample task with three samples (2 s, 6 s, and 18 s) and two comparisons (red and green). In the asymmetrical task, 6-s and 18-s samples shared the same comparison. In a subsequent retention test, both groups showed a preference for the comparison associated with the longer samples, a result consistent with the hypothesis that pigeons based their choices on the duration elapsed since the offset of the houselight (i.e., sample duration + retention interval). Results from two no-sample tests further corroborated the importance of the ITI illumination as a time marker: When the ITI was illuminated, the proportion of choices correlated positively with the retention interval; when the ITI was darkened, choices fell to random levels. However, the absolute value of choice proportions suggested that the sample stimulus was also a time marker. How multiple stimuli acquire control over behavior and how they combine remains to be worked out.  相似文献   

5.
In two experiments, we investigated emergent conditional relations in pigeons using a symbolic matching-to-sample task with temporal stimuli as the samples and hues as the comparisons. Both experiments comprised three phases. In Phase I, pigeons learned to choose a red keylight (R) but not a green keylight (G) after a 1-s signal. They also learned to choose G but not R after a 4-s signal. In Phase II, correct responding consisted of choosing a blue keylight (B) after a 4-s signal and a yellow keylight (Y) after a 16-s signal. Comparisons G and B were both related to the same 4-s sample, whereas comparisons R and Y had no common sample. In Phase III, R and G were presented as samples, and B and Y were presented as the comparisons. The choice of B was correct following G, and the choice of Y was correct following R. If a relation between comparisons that shared a common sample were to emerge, then responding to B given G would be more likely than responding to Y given R. The results were generally consistent with this prediction, suggesting, for the first time in pigeons, the emergence of novel relations that involve temporal stimuli as nodal samples.  相似文献   

6.
In Experiment 1, pigeons were trained to discriminate short (2 sec) and long (8 sec) durations of tone by responding to red and green comparison stimuli. During delay testing, a systematic response bias to the comparison stimulus correct for the long duration occurred. Tests of responding without the tone reduced accuracy on long-sample trials but not on short-sample trials suggesting that the pigeons were attending to the tone and not simply timing the total trial duration. The pigeons were then trained to match short (2 sec) and long (8 sec) durations of light to blue/yellow comparisons. During delay testing, “choose-long errors” occurred following tone durations, but “choose-short errors” occurred following light durations. In Experiment 2, accuracy was assessed on test trials in which the tone and the light signals were simultaneously presented for the same duration or for different durations. Pigeons responded accurately to durations of light, but were unable to accurately respond to durations of tone simultaneously presented with the light. The data from Experiment 1 suggest that there are important differences between light and tone signals with respect to the events that control the termination of timing. The data from Experiment 2 indicate that pigeons cannot simultaneously time visual and auditory signals independently and without interference. Consequently, they are inconsistent with the idea that there is a single internal clock that times both tone and light durations.  相似文献   

7.
Pigeons performed a delayed matching-to-sample task in which they matched red and green disks as comparison stimuli to samples of food and no food. The birds were also taught a discrimination between two lines: vertical (S+) followed by food and horizontal (S?) followed by no food. The two kinds of trials were then chained in infrequent probes such that (a) S+ and S? preceded samples of food and no food, (b) a longer than usual delay occurred, and then, (c) the comparison stimuli were presented. Therefore, in probes when S+ preceded food and S? preceded no food, the samples were “expected. ” But in probes when S+ signaled no food and S? signaled food, the samples were “surprising. ” Matching to surprising samples was more accurate than matching to expected samples. This result completes a pattern of findings implying that surprising reinforcers enhance learning and also persist (are longer rehearsed) in short-term memory.  相似文献   

8.
Pigeons were trained on delayed matching-to-sample trials in which red and green sample stimuli were equally often followed by color comparisons and by line-orientation comparisons. The color samples were preceded and accompanied by cues (a triangle or a black dot) that signaled whether the comparisons on that trial would be colors or lines. Length of the retention interval was manipulated during testing, and probe trials were included on which the dimension of the comparison stimuli either was cued incorrectly or was not cued. Accuracy on incorrectly cued and on no-cue trials was less than that on correctly cued trials, and the magnitude of this effect was not influenced by the length of the retention interval. Accuracy on incorrectly cued and on no-cue trials was equivalent, and was greater than chance. The data are inconsistent with two dual-coding interpretations of the effects of incorrectly cuing the dimension of the comparison stimuli in which it is held that both retrospective and prospective sample coding occurs in this task.  相似文献   

9.
In simultaneous matching-to-sample and oddity-from-sample tasks, briefly delaying the offset of trial stimuli following an incorrect choice response was found to facilitate task acquisition (Experiment 1). Because thispenalty-time procedure also resulted in longer choice-response latencies, it was hypothesized that any procedure that increased response latency would facilitate task acquisition. However, in Experiment 2, no evidence of facilitation was found when a 2-sec pause was imposed prior to the choice response. The results of Experiment 3 suggest that penalty-time facilitation of acquisition was not due to either the added differential outcome on correct versus incorrect trials (i.e., incorrect choice responses do not darken the keys as do correct choice responses) or the aversive effects associated with trial prolongation (i.e., incorrect responses not only result in the absence of reinforcement but also delay the start of the next trial). Instead, results suggest that birds trained with the penalty-time procedure review the trial stimuli following an incorrect choice.  相似文献   

10.
Color discrimination ability can be determined through anatomy or perceptual ability. In this study we tested perceptual ability. Three Asian small-clawed otters (Aonyx cinerea), one male and two females, were trained via operant conditioning to discriminate stimuli within a training task. If they passed criteria for this task, they were tested on as many as six delayed matching-to-sample experimental tasks. These experimental tasks involved comparing varying saturations of the colors blue, green, and red against varying shades of gray, as well as against each other. The male reached criterion on five of the experimental tasks, indicating an ability to discriminate the stimuli. One female participated in only two tasks and did not achieve the criteria as set. The second female did not pass the training task, and thus was not experimentally tested. This study overall showed some early evidence that Asian small-clawed otters may have the ability to learn to discriminate different stimuli on the basis of color cues. Sensory studies conducted on two other otter species and the results of this study indicate that color vision may be a common trait across Lutrinae species.  相似文献   

11.
Pigeons were trained in a two-choice delayed matching-to-sample task with red and green hues. A brief postsample cue (a vertical or horizontal line) signaled whether the comparison stimuli would be presented or omitted on each trial. Comparison stimuli were always presented following the remember (R) cue, but never following the forget (F) cue or no-cue trials. One group of birds, the differential outcome (DO) group, received reinforcement with a probability of 1.0 for correct responses following one sample stimulus and a probability of 0.2 for correct responses following the other sample stimulus. The nondifferential outcome (NDO) group received reinforcement with a probability of 0.6 for correct responses to either stimulus. The effect of postsample cues was greater for the DO group than for the NDO group. Relative to the NDO group, the DO group displayed higher accuracy on R-cue trials and lower accuracy on F- and no-cue trials. Both tendencies contributed to the enhanced cue effectiveness obtained in the DO group. The results indicate that outcome expectancies are subject to maintenance rehearsal, which comes under the control of postsample R and F cues. They also suggest that maintenance rehearsal may be easier to sustain under DO conditions than under NDO conditions when a memory test is anticipated, but that it may be easier to terminate maintenance rehearsal under DO conditions when a memory test is not anticipated. The results are inconsistent with the assumption that the rehearsal of outcome expectancies is automatic.  相似文献   

12.
In the present experiment, we compared directly pigeons’ short-term memory of temporal and visual stimuli in a delayed matching-to-sample task. The sample stimuli consisted of red and green lights presented for 5 and 30 sec, followed by a retention interval and blue and yellow comparisons. For subjects in the visual group, duration was irrelevant and the color of the sample was the conditional cue. For animals in the temporal group, color was irrelevant and duration of the sample was the conditional stimulus. The results showed that acquisition of the matching task was faster and accuracy was higher in the visual than in the temporal group. More importantly, memory of either sample generally declined at a similar rate when the duration of the retention interval was increased and when the intertrial interval was reduced. Taken together, the results indicate that with 1–8-sec retention intervals, short-term memory for temporal stimuli is similar to that found with color-visual samples. The findings are discussed in terms of retrospective and prospective processing.  相似文献   

13.
Common coding in pigeons was examined using a delayed conditional discrimination in which each sample stimulus was associated with two different comparison stimuli (one-to-many mapping). In Experiment 1, pigeons matched circle and dot samples to red and green hues and vertical and horizontal line orientations. In Experiment 2, the samples were red and green and the comparisons were vertical and horizontal spatial positions (up vs. down and left vs. right). Following acquisition to high levels of accuracy in each experiment, the associations between the samples and either both sets or only one set of comparisons were reversed. Pigeons learned the total reversals faster than the partial reversals. These results suggest that when different comparisons are associated with a common sample, they may become functionally equivalent.  相似文献   

14.
Pigeons were trained in a two-choice delayed matching-to-sample task with red and green hues. A brief postsample cue (a vertical or horizontal line) signaled whether the comparison stimuli would be presented or omitted on each trial. Comparison stimuli were always presented following the remember-cue (R-cue) trial, but never following the forget-cue (F-cue) and no-cue trials. In Experiment 1, matching accuracy on F-cue and no-cue trials was equivalent and was considerably inferior to accuracy on R-cue trials. In Experiment 2, the placement of the postsample cue was manipulated. Matching accuracy decreased as the R cue was delayed in the retention interval, but performance in the F-cue condition was not affected. These data indicate that the no-cue condition can function as an implicit F cue and that the R cue can function to initiate and maintain rehearsal.  相似文献   

15.
Selective attention in processing of visual information by pigeons, trained on alternating sessions with two colors (red and green) and two forms (a diamond and an X shape) differentially associated with a left—right key choice task, was examined. A color and a form were presented together on probe trials during sessions in which, on other trials, only one of the dimensions, color or form, was shown. The dimension in effect on the surrounding trials had no influence on choice when the information provided by the two dimensions on probe trials was in conflict—color correct for one choice and form for the other. When both color and form redundantly cued the correct choice, there was no increase in accuracy in comparison with that associated with one dimension. Following separate training on the color and form discriminations, pigeons appeared to base their choices on color on some trials, on form on other trials, but not on both simultaneously. These findings are discussed in terms of an exemplar model of information processing.  相似文献   

16.
In two matching-to-sample experiments, pigeons’ performance with samples of stimuli (red and green), number of responses (1 and 20), and reinforcers (food and no food) was assessed. Samples of red, 20 responses, and food were associated with the red comparison stimulus, and samples of green, 1 response, and no food were associated with the green comparison stimulus. On interference trials, three sample types were presented on each trial, and two of the samples (congruent) were associated with the correct comparison and the third sample (incongruent), with the incorrect comparison. Performance on interference trials was compared with that on control trials in which either two (Experiment 1) or three (Experiment 2) congruent samples were presented. It was found that presentation of an incongruent sample reduced matching accuracy markedly, and about equally, whether samples were presented successively or in compound. Although the type of sample that was incongruent was without effect, matching accuracy declined strongly as the recency of the incongruent sample increased. Serial position of the incongruent sample also influenced the shape of the retention function on interference trials. Presentation of the incongruent sample either first or second resulted in accuracy decreasing across the retention interval, whereas presentation of the incongruent sample last in the input sequence resulted in increasing accuracy across the retention interval. The theoretical implications of the findings are considered.  相似文献   

17.
Pigeons’ performance of a delayed conditional discrimination with presence versus absence of conditional (sample) stimuli was examined in two experiments. The pigeons showed steeper retention functions with feature (i.e., presence) samples (either food or yellow) than with no-feature (i.e., absence) samples (either no food or no yellow). These results suggest that pigeons code features and respond only by default to test stimuli (comparisons) associated with no features. In contrast, the overall superiority of performance on no-feature-sample trials compared with feature-sample trials in both the food/no-food- and yellow/no-yellow-sample tasks was reversed at a 0-sec delay in the food/no-food-sample group, but not in the yellow/non-yellow-sample group. This difference in results with hedonic versus nonhedonic samples suggests that the crossover in delay performance on food/no-food-sample trials is produced by the formation of backward associations between the food-associated comparison stimulus and the food sample.  相似文献   

18.
Match-to-sample and oddity-from-sample problems with four colors were acquired by two pigeons under the supraordinate control of a line tilt superimposed on samples, Since the supraordinate stimulus terminated before the comparison stimuli were presented, accurate matching and oddity performance indicated trace stimulus control as well, The temporal extent of trace control was assessed in one subject by presenting probes—trials without a line tilt on the sample—in which the basis of correct responding was the supraordinate stimulus presented on the previous trial, Trace supraordinate control did not extend between trials, Subsequently, the delay between the termination of the supraordinate stimulus and the presentation of the comparison stimuli was gradually increased within a trial, Both subjects were able to perform matching and oddity over longer delays, and eventually on probe trials, although accuracy decreased, Results were discussed in terms of instructional stimulus control and memory.  相似文献   

19.
In Experiment 1, pigeons were trained to discriminate the duration (2 or 8 sec) of an empty interval separated by two 1325-Hz tone markers by responding to red and green comparison stimuli. During delay testing, a choose-short bias occurred at 1 sec, but a robust choose-long bias occurred at 9 sec. Responding in the absence of tone markers indicated that the pigeons were attending to the markers and not simply timing the total trial duration. The birds were then trained to match short (2-sec) or long (8-sec) empty intervals marked by light to blue/yellow comparisons. For both visual and auditory markers, delay testing produced a choose-short bias at 1 sec and a choose-long bias at 9 sec. In Experiment 2, the pigeons were shifted from a fixed to variable intertrial intervals (ITI) within sessions. On trials with tone markers, the duration of both the empty interval and the preceding ITI affected choice responding. On trials with light markers, only the duration of the empty interval influenced choice responding. Subsequent delay testing in the context of variable ITIs replicated the memory biases previously obtained. In Experiment 3, performance was assessed at various delay intervals on trials in which either the first or the second marker was omitted. The data from these omission tests indicated that the first marker initiated timing but that the second marker sometimes initiated the timing of a new interval. Explanations of these effects in terms of the internal clock model of timing are discussed, and a simple quantitative model of the delay interval data is tested.  相似文献   

20.
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   

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