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1.
In three experiments, we examined pigeons’ recognition of video images of human faces. In Experiment 1, pigeons were trained to discriminate between frontal views of human faces in a go/no-go discrimination procedure. They then showed substantial generalization to novel views, even though human faces change radically as viewpoint changes. In Experiment 2, the pigeons tested in Experiment 1 failed to transfer to the faces dynamically rotating in depth. In Experiment 3, the pigeons trained to discriminate the dynamic stimuli showed excellent transfer to the corresponding static views, but responses to the positive faces decreased at novel viewpoints outside the range spanned by the dynamic stimuli. These results suggest that pigeons are insensitive to the three-dimensional properties of video images. Consideration is given to the nature of the task, relating to the identification of three-dimensional objects and to perceptual classifications based on similarity judgments.  相似文献   

2.
In three experiments, pigeons were trained to discriminate between uniform arrays of two elements that differed in color, form, or size. They were then tested with arrays that contained different proportions of the two elements on these dimensions. In all cases, orderly discrimination gradients reflected these proportions. The discrimination readily transferred to new arrays with similar stimuli, but with different total numbers of elements. In Experiment 4, the pigeons were taught to discriminate between two groups of categorical stimuli: pictures of birds and pictures of flowers. A test with different proportions of each again produced a gradient based on relative numerosity. Experiment 5 demonstrated transfer of stimulus control on the numerosity dimension when pigeons were trained with one set of instances from two categories, and then were tested with new instances from the same categories.  相似文献   

3.
In two experiments, we examined the discrimination of photographs of individual pigeons by pigeons, using go/no-go discrimination procedures. In Experiments 1A and 1B, the pigeons were trained to discriminate 4 photographs of one pigeon from those of a number of pigeons. The subjects learned the discrimination, but their discriminative behavior did not transfer to new photographs taken from novel perspectives. When the pigeons were trained to discriminate between 20 photographs of five pigeons taken from four perspectives as the S+ and 20 photographs of five different pigeons as the S-, the subjects learned the discrimination, and this discriminative behavior partially transferred to new photographs taken from novel perspectives (Experiments 2A-2C). The results suggest that pigeons are able to discriminate among conspecific individuals, using stationary visual cues. This strengthens the assumption in evolutionary theory that animals can discriminate among individuals and encourages further investigation as to how this ability is used in various behaviors of animals.  相似文献   

4.
We investigated whether pigeons are able to discriminate color photographs of male and female pigeons, using a categorical discrimination procedure. In Experiments 1 and 2B, 10 out of 14 pigeons learned the discrimination. Of these, 5 pigeons showed transfer to novel stimuli, demonstrating the categorical nature of the trained discrimination. Experiment 3 showed that the discriminative behavior was based primarily on the body, as opposed to the head and the neck region. In 1 out of 3 pigeons, the discriminative behavior was maintained by the black-and-white photographs. The results suggest that some pigeons have the ability to discriminate the sex of conspecifics without behavioral cues.  相似文献   

5.
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   

6.
Pigeons were trained on an operant procedure to discriminate between morning and afternoon when location did not vary (Experiment 1). The pigeons were placed on a fixed interval (FI) schedule in the morning and on a different FI schedule in the afternoon. Probe trials that occurred at the beginning of the training sessions were examined. The pigeons responded differently, depending on the time of day, reflecting the learning of a stable 24-h memory representation of the association between the FI schedules and the time of day. The pigeons from Experiment 1 were then clock shifted and tested twice, to determine whether they were relying on an endogenous circadian oscillator, an hourglass mechanism influenced by the photoperiod, or environmental noise to make the time-of-day discrimination (Experiment 2). The results of the second experiment indicated a circadian mechanism was most important for the observed time-of-day learning.  相似文献   

7.
Eight homing pigeons, trained to fly between two elevated feeders within a flight tunnel, were tested for their ability to discriminate between two magnetic field stimuli and two acoustic stimuli, using a unitary discrete-trials procedure with successive presentation of stimuli. Magnetic stimuli consisted of the ambient magnetic field and a reduced magnetic field in which the vertical component of the field was reduced to 50% of its ambient value. Acoustic stimuli consisted of an ambient white noise and the white noise plus a tone. Stimuli were paired with food reward and either a time penalty (Experiment 1) or electric shock (Experiment 2). Although subjects could discriminate sounds with our procedures, none of the subjects demonstrated discrimination of magnetic fields. The failure of pigeons to discriminate magnetic stimuli is discussed as a consequence of either the failure to provide conditions sufficient for such discrimination or the absence of a magnetic sense in these animals.  相似文献   

8.
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   

9.
Pigeons and adult humans searched for a 2-cm2 unmarked goal in digitized images of an outdoor scene presented on a touch-screen monitor. In Experiment 1, the scene contained three landmarks near the goal and a visually rich background. Six training images presented the scene from different viewing directions and distances. Subsequent unreinforced tests in which landmark or background cues were removed or shifted revealed that pigeons’ search was controlled by both proximal landmarks and background cues, whereas humans relied only on the proximal landmarks. Pigeons’ search accuracy dropped substantially when they were presented with novel views of the same scene, whereas humans showed perfect transfer to novel views. In Experiment 2, pigeons with previous outdoor experience and humans were trained with 28 views of an outdoor scene. Both pigeons and humans transferred well to novel views of the scene. This positive transfer suggests that, under some conditions, pigeons, like humans, may encode the three-dimensional spatial information in images of a scene.  相似文献   

10.
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   

11.
A go/no-go procedure was used to train pigeons to discriminate pictures of human faces differing only in shape, with either static images or movies of human faces dynamically rotating in depth. On the basis of experimental findings in humans and some earlier studies on three-dimensional object perception in pigeons, we expected dynamic stimulus presentation to support the pigeon’s perception of the complex morphology of a human face. However, the performance of the subjects presented with movies was either worse than (AVI format movies) or did not differ from (uncompressed dynamic presentation) that of the subjects trained with a single or with multiple static images of the faces. Furthermore, generalization tests to other presentation conditions and to novel static views revealed no promoting effect of dynamic training. Except for the subjects trained on multiple static views, performance dropped to chance level with views outside the training range. These results are in contrast to some prior reports from the literature, since they suggest that pigeons, unlike humans, have difficulty using the additional structural information provided by the dynamic presentation and integrating the multiple views into a three-dimensional object.  相似文献   

12.
The effects of identical context on pattern recognition by pigeons for outline drawings of faces were investigated by training pigeons to identify (Experiment 1) and categorize (Experiment 2) these stimuli according to the orientation of the mouth—an upright U shape representing a smiling mouth or an inverted U shape representing a sad mouth. These target stimuli were presented alone (Pair 1), with three dots in a triangular orientation to represent a nose and eyes (Pair 2), and with the face pattern surrounded by an oval (Pair 3). In Experiment 1, the pigeons trained with Pair 1 were most accurate, those trained with Pair 2 were less so, and those trained with Pair 3 failed to acquire the discrimination within eighty 100-trial sessions. The same ordering was found in Experiment 2 for pigeons trained on the three pairs simultaneously. The authors suggest that a contrasting finding in humans, the face superiority effect, might be due to a gain in discriminability resulting from recognition of the pattern as a face. An exemplar model of information processing that excludes linguistic coding accounts for the present results.  相似文献   

13.
Discrimination and memory for video films of women performing different activities was investigated in 5.5 month-old infants. In Experiment 1, infants (N = 24) were familiarized to the faces of one of three women performing one of three repetitive activities (blowing bubbles, brushing hair, and brushing teeth). Overall, results indicated discrimination and memory for the actions but not the faces after both a 1-min and a 7-week delay. Memory was demonstrated by a visual preference for the novel actions after the 1-min delay and for the familiar actions after the 7-week delay, replicating prior findings that preferences shift as a function of retention time. Experiment 2 (N = 12) demonstrated discrimination and memory for the faces when infants were presented in static poses at the 1-min delay, but not the 7-week delay. In Experiment 3 (N = 18), discrimination of the actions was replicated, but no discrimination among the objects embedded in the actions (hairbrush, bubble wand, toothbrush) was found. These findings demonstrate the attentional salience of actions over faces in dynamic events to 5.5 month-olds. They highlight the disparity between results generated from moving versus static displays in infancy research and emphasize the importance of using dynamic events as a basis for generalizing about perception and memory for events in the real world.  相似文献   

14.
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   

15.
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   

16.
In two experiments, we examined how preexposure to discriminative stimuli and introduction of a 21-day retention interval affected the latent inhibition (LI) and perceptual learning (PL) of rats in a choice-maze discrimination task. Experimental groups were preexposed to three wall patterns, one in each of three arms of a maze. Control groups were preexposed only to white arms. PL groups were trained to discriminate A versus B, and LI groups, to discriminate A or B versus C. The A and B patterns shared many elements not shared with the C pattern. In Experiment 1, both at the end of training and after the subsequent retention interval, the PL groups performed better than controls, whereas the LI groups performed worse. In Experiment 2, inserting the 21-day retention interval between preexposure and discrimination training disrupted final measures of LI but not PL performance. Implications for current concepts of PL and LI are discussed.  相似文献   

17.
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   

18.
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   

19.
According to the mixed memory model (Penney, Gibbon, & Meck, Journal of Experimental Psychology: Human Perception and Performance, 26, 1770–1787, 2000), different clock rates for stimuli with different nontemporal properties must be stored within a single reference memory distribution in order to detect a difference between the clock rates of the different signals. In Experiment 1, pigeons were trained in a between-subjects design to discriminate empty intervals (bound by two 1-s visual markers) and filled intervals (a continuous visual signal). The intervals were signaled by different visual stimuli, and they required responses to different sets of comparison stimuli. Empty intervals were judged as being longer than filled intervals. The difference between the point of subjective equality (PSE) for the empty intervals and the PSE for the filled intervals increased proportionally as the magnitudes of the anchor duration pairs were increased from 2 and 8 s to 4 and 16 s. In Experiment 2, the pigeons were trained to discriminate intervals signaled by the absence of houselight illumination (Group Empty) or the presence of houselight illumination (Group Filled). The psychophysical timing functions for these intervals were identical to each other. The results of Experiment 1 indicate that memory mixing is not necessary for detecting a timing difference between empty and filled intervals in pigeons. The results of Experiment 2 suggest that the nature of the stimuli that signal the empty and filled intervals impacts how pigeons judge the durations of empty and filled intervals.  相似文献   

20.
We investigated the role of dynamic information in human and pigeon object recognition. Both species were trained to discriminate between two objects that each had a characteristic motion, so that either cue could be used to perform the task successfully. The objects were either easy or difficult to decompose into parts. At test, the learned objects could appear in their learned motions, the reverse of the learned motions, or an entirely new motion, or a new object could appear in one of the learned motions. For humans, any change in the learned motion produced a decrement in performance for both the decomposable and the nondecomposable objects, but participants did not respond differentially to new objects that appeared in the learned motions. Pigeons showed the same pattern of responding as did humans for the decomposable objects, except that pigeons responded differentially to new objects in the learned motions. For the nondecomposable objects, pigeons used motion cues exclusively. We suggest that for some types of objects, dynamic information may be weighted differently by pigeons and humans.  相似文献   

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