Stimulus properties of conspecific behavior

Two experiments identified the conditions in which the behavior of one bird acquired discriminative control of the behavior of a second bird. The schedule-controlled behaviors of the “stimulus” bird were differentially correlated with the components of a multiple schedule according to which the pecking of an “experimental” bird produced food. In Experiment 1, three pairs of pigeons acquired a successive discrimination and two reversals with the conspecific stimuli. Experiment 2 included a control condition in which no systematic relationship existed between the conspecific stimuli and the component schedules. While differential responding during the components of the multiple schedule was again found when the conspecific stimuli were available, differential responding did not occur in the control condition. Test conditions included in the experiments indicated that (a) the differential responding was not dependent on the discriminative properties of reinforcement, (b) the pecking of the stimulus and experimental birds was temporally interrelated, (c) the visual conspecific stimuli were critical to the maintenance of the discrimination, and (d) the observed stimulus control immediately generalized to an unfamiliar conspecific.     

The effectiveness of fading in programming a simultaneous form discrimination for retarded children

A non-verbal teaching program, combined with reinforcement and extinction (Program Group), was compared with reinforcement and extinction alone (Test Group) in teaching retarded children to discriminate circles from ellipses. In the Program Group, fading techniques were used to transfer stimulus control from “bright vs. dark” to “form vs. no-form” and then to “circle vs. ellipse”. The Test Group had the task of learning the circle-ellipse discrimination with no prior teaching program. With the program, seven of 10 children learned the circle-ellipse discrimination. Without the program, one of nine learned. The eight Test-Group children who failed to learn circle vs. ellipse were then given the opportunity to learn the form no-form discrimination by reinforcement and extinction alone, without fading. Six of the eight learned, but only three of these six then learned circle vs. ellipse on a second test. All seven Program-Group children who had learned form vs. no-form also learned the circle-ellipse discrimination by means of fading; each of the seven made fewer errors than any of the three who succeeded on the second test. Children who failed to learn circle vs. ellipse adopted response patterns incompatible with the development of appropriate stimulus control.     

Stress-induced breakdown of an appetitive discrimination

Rats trained to discriminate between S^D and S^Δ for food reinforcement showed marked impairments in this discrimination when strong, unavoidable shocks occurred at the termination of a third stimulus. The predominant feature of this impairment was a supernormal rate of unreinforced (S^Δ) behavior. Shocks delivered without exteroceptive warning also led to a discriminative breakdown. The effect was a direct function of shock intensity. When behavior was strongly suppressed in the third stimulus by response-correlated shock (“punishment”), instead of unavoidable shock, breakdowns were only temporary; as soon as responding recovered from its overall suppression, discriminative performance returned to normal. The discriminative deterioration may be interpreted as an emotional by-product of frequent aversive stimulation, but accidental contingencies could also have played a role.     

Selective attention: the effects of combining stimuli which control incompatible behavior

Four rhesus monkeys learned both a color and tilt discrimination. The stimuli were combined to produce incompatible behavior. The behavior controlled by one set of stimuli was reinforced until “errors” virtually disappeared. The stimuli were tested separately again. Sixteen replications of the entire procedure indicated that the stimuli producing “errors” were ignored.     

Recognition by the pigeon of stimuli varying in two dimensions

Pigeons served in four experiments, each of which involved about 44,000 discrete 1.2-sec trials under steady-state conditions. The first experiment scaled a short segment of the visual wavelength continuum; this dimension was then combined in a conditional discrimination with each of three others; time after reinforcement, tone frequency, and line tilt. In the two-stimulus experiments, the birds' responses were reinforced in the presence of only one stimulus combination: “582 nm” together with “2 min after reinforcement”, “3990 Hz”, or “vertical line”. Many other stimulus combinations also appeared equally often and went without reinforcement. The wavelength stimuli conformed to an equal-interval scale, and per cent response was generally linear with wavelength, when scaled on cumulative normal coordinates. The components of the compound stimulus were found to interact in a multiplicative fashion; when one component differed greatly from its reinforcement value, changes in the other component had relatively little effect. For the “time”-“wavelength” compound, this interaction appeared to be modified by the effects of set or attention. Certain response latency data are reported, and other combination rules are discussed.     

Discrimination of intentional and random motion paths by pigeons

Twelve pigeons (Columba livia) were trained on a go/no-go schedule to discriminate between two kinds of movement patterns of dots, which to human observers appear to be "intentional" and "non-intentional" movements. In experiment 1, the intentional motion stimulus contained one dot (a "wolf") that moved systematically towards another dot as though stalking it, and three distractors ("sheep"). The non-intentional motion stimulus consisted of four distractors but no stalker. Birds showed some improvement of discrimination as the sessions progressed, but high levels of discrimination were not reached. In experiment 2, the same birds were tested with different stimuli. The same parameters were used but the number of intentionally moving dots in the intentional motion stimulus was altered, so that three wolves stalked one sheep. Despite the enhanced difference of movement patterns, the birds did not show any further improvement in discrimination. However, birds for which the non-intentional stimulus was associated with reward showed a decline in discrimination. These results indicated that pigeons can discriminate between stimuli that do and do not contain an element that human observer see as moving intentionally. However, as no feature-positive effect was found in experiment 1, it is assumed that pigeons did not perceive or discriminate these stimuli on the basis that the intentional stimuli contained a feature that the non-intentional stimuli lacked, though the convergence seen in experiment 2 may have been an effective feature for the pigeons. Pigeons seem to be able to recognise some form of multiple simultaneously goal-directed motions, compared to random motions, as a distinctive feature, but do not seem to use simple "intentional" motion paths of two geometrical figures, embedded in random motions, as a feature whose presence or absence differentiates motion displays. Electronic Publication     

Reinforcement duration and the peak shift in post-discrimination gradients

Pigeons were trained to key-peck for food, first with single-stimulus training and then with successive discrimination (multiple schedule) training. In the multiple schedule, two different wavelengths were each correlated with equally frequent variable-interval reinforcement but different durations (6 sec vs. 2 sec) of access to grain. For some birds, the different durations of feeding cycle were cued by different intensities of the food hopper light. For some of these “cued” birds, single-stimulus training had been carried out with 6-sec feedings and when multiple-schedule training was introduced, the novel stimulus was correlated with 2-sec feedings. For the others, 2-sec feedings were originally used, and the novel stimulus was then present during the 6-sec reinforcement duration. The cueing procedure enhanced discrimination performance, and was necessary for the consistent production of a peak shift. In addition, the condition in which original training had been carried out with 6-sec feedings, and thus reinforcement duration was reduced in the presence of the novel stimulus, led to the best performance.     

Pigeons can discriminate “good” and “bad” paintings by children

Humans have the unique ability to create art, but non-human animals may be able to discriminate “good” art from “bad” art. In this study, I investigated whether pigeons could be trained to discriminate between paintings that had been judged by humans as either “bad” or “good”. To do this, adult human observers first classified several children’s paintings as either “good” (beautiful) or “bad” (ugly). Using operant conditioning procedures, pigeons were then reinforced for pecking at “good” paintings. After the pigeons learned the discrimination task, they were presented with novel pictures of both “good” and “bad” children’s paintings to test whether they had successfully learned to discriminate between these two stimulus categories. The results showed that pigeons could discriminate novel “good” and “bad” paintings. Then, to determine which cues the subjects used for the discrimination, I conducted tests of the stimuli when the paintings were of reduced size or grayscale. In addition, I tested their ability to discriminate when the painting stimuli were mosaic and partial occluded. The pigeons maintained discrimination performance when the paintings were reduced in size. However, discrimination performance decreased when stimuli were presented as grayscale images or when a mosaic effect was applied to the original stimuli in order to disrupt spatial frequency. Thus, the pigeons used both color and pattern cues for their discrimination. The partial occlusion did not disrupt the discriminative behavior suggesting that the pigeons did not attend to particular parts, namely upper, lower, left or right half, of the paintings. These results suggest that the pigeons are capable of learning the concept of a stimulus class that humans name “good” pictures. The second experiment showed that pigeons learned to discriminate watercolor paintings from pastel paintings. The subjects showed generalization to novel paintings. Then, as the first experiment, size reduction test, grayscale test, mosaic processing test and partial occlusion test were carried out. The results suggest that the pigeons used both color and pattern cues for the discrimination and show that non-human animals, such as pigeons, can be trained to discriminate abstract visual stimuli, such as pictures and may also have the ability to learn the concept of “beauty” as defined by humans.     

Programming stimuli in matching to sample

In these investigations, a “teaching machine” was used to train pre-school and first-grade children in a series of progressively difficult discrimination tasks, leading up to matching to sample. Such training was much more efficient than training in the final discrimination alone. The errors the subjects made were found to be a functon both of the differences between consecutive discriminations (the “size of the steps” in the program) and the length of training on each discrimination. Theoretical and practical implications of these findings are discussed.     

Complex learning and information processing by pigeons: a critical analysis

Three models of conditional discrimination learning by pigeons are described: stimulus configuration learning, the multiple-rule model, and concept learning. A review of the literature reveals that true concept learning is not characteristic of the behavior of pigeons in matching-to-sample, oddity-from-sample, or symbolic matching studies. Instead, pigeons learn a set of sample-specific S^D rules. Transfer of the discrimination to novel stimuli, at least along the hue dimension, is predicted by a “coding hypothesis”, which holds that pigeons make a unique, but usually unobserved response, R₁, to each sample, and that the comparison stimulus chosen depends on which R₁ was emitted in the presence of the sample. Convincing evidence is found that pigeons do code sample hues, but there is little evidence that allows one to infer that the “coding event” must have behavioral properties. Parameters of the conditional discrimination paradigm are identified, and it is shown that by appropriate parametric manipulation, a variety of analogous tasks may be generated for both human and animal subjects. The tasks make possible the comparative study of complex learning, attention, memory, and information processing, with the added advantage that behavior processes may be compared systematically across tasks.     

The effect of overtraining on behavioral contrast and the peak-shift

Following initial discrimination training between two wavelength stimuli and a subsequent generalization test to the wavelength dimension, Group 1 was “overtrained” for 105 days on the original discrimination. Group 2 was “overtrained” with the original positive stimulus and a new negative stimulus, a white line. Group 3 was “overtrained” with the original negative stimulus and a new positive stimulus, the white line. Each 15 days of extended training were followed by a wavelength generalization test similar to the first test. The results suggest that there is no consistent relationship between the response rate in positive stimulus immediately before the generalization test and whether or not a peak shift occurs during the test.     

Average uncertainty as a determinant of observing behavior

After discrimination training on a multiple variable-interval extinction schedule of food reinforcement, pigeons were placed on the uncued or mixed version of the same schedule and allowed to make an optional “observing response” that converted the uncued schedule to the corresponding cued schedule by providing a 20-sec exposure to the appropriate discriminative stimulus. The schedule consisted of one hundred 40-sec components, and the probability that any one of them would be a variable-interval component was systematically varied between 0.00 and 1.00. The results showed that the amount of observing behavior was an inverted “U” function of the probability of the variable-interval component. Few observing responses occurred at probabilities of 0.00 or 1.00, and maximum responding occurred at a value less than 0.50.     

Pigeons can discriminate locations presented in pictures

The present experiments were designed to teach pigeons to discriminate two locations represented by color photographs. Two sets of photographs were taken at two distinctive locations on a university campus. These sets represented several standpoints at each location. For the true-discrimination group, pictures from the two locations were differentially associated with reward; for the pseudodiscrimination group, half of the views from each location were arbitrarily but consistently associated with reward. The former group acquired the discrimination much more rapidly. These birds also showed good transfer to new views from the standpoints used in training and to a new standpoint at each location not used in training. In a second experiment, another group of pigeons could terminate any training trial by pecking an “advance” key. Three of 4 subjects used this option to reduce the duration of trials in which pictures from the negative location were presented. These data suggest that pigeons can integrate views shown in pictures into a “concept” of a location. The method used here may be the experimental analogue of a common, natural process by which animals learn to identify locations.     

Generalization gradients of inhibition after different amounts of training

Five groups of pigeons received seven sessions of variable-interval reinforcement for pecking a blank white key, followed by either 1, 2, 4, 8, or 16 sessions of training on a successive discrimination in which the positive stimulus was the blank white key and the negative stimulus was a black vertical line on the white key. After training, a generalization test was administered along the line-tilt continuum. Relative gradients of inhibition became steeper with increased amounts of training, and reliably nonhorizontal absolute gradients were obtained only from groups of subjects with at least four days of training. Therefore, inhibitory stimulus control improves with added training. Several problems with the concept of “inhibition” are examined and some implications of the results for theoretical analyses of operant discrimination learning are discussed.     

Shape discrimination and concept formation in the jungle crow (Corvus macrorhynchos)

We investigated whether jungle crows can learn concepts by using printouts of shapes in a simultaneous two-alternative task. Jungle crows were first trained with a red triangle and red square until they reached the discrimination criterion (80 % of correct choices in two blocks of 10 trials each). Then, we tested crows with successive transfer tests to investigate both the discrimination cues being used and concept formation ability, by using novel triangular and non-triangular stimuli. All of the jungle crows learnt to discriminate between the triangle and square during training. The discrimination performance was generally not affected either by changes in the colour of the stimuli or when both shape and colour cues conflicted, with the previously non-rewarded shape but matching colour (red square) versus rewarded shape but non-matching colour (green triangle). The use of only outlines of the familiar stimuli also did not affect discrimination behaviour of crows. In addition, crows significantly discriminated novel triangular shapes during the limited trials given, suggesting their ability to form the concept of triangularity. However, failure to discriminate when the novel stimuli size deviated from the original suggests that there is a limit to shape concept formation in a familiar–novel context in the jungle crow.     

Inhibitory control and errorless discrimination learning

Pigeons learned to discriminate between a positive stimulus (white key) and a negative stimulus (red or green key, depending on the subject) via Terrace's fading procedure. Generalization tests, conducted with intermittent reinforcement for key pecking at various wavelengths, yielded minima at the value of the negative stimulus in most “errorless” birds. Terrace's contrary finding of flat gradients in errorless subjects probably resulted from a floor-effect (i.e., virtually zero responding) produced by his extinction-test procedure. The present and other findings do not support Terrace's conclusions that the negative stimulus of an errorless discrimination is behaviorally neutral; inhibition apparently develops to the nonreinforced stimulus even during errorless discrimination learning. A negative correlation between stimulus and reinforcer seems the crucial factor in producing an inhibitory stimulus.     

Fading and errorless transfer in successive discriminations

A successive discrimination between red positive and green negative stimuli was established with pigeon subjects. Then, lines with different angular orientations were superimposed on one of the colors to form compound stimuli. Finally, either the colored element of the positive compound, the colored element of the negative compound, or both colored elements together, were gradually attenuated. Before each attenuation, the line elements were presented alone against dark backgrounds as probes to assess the degree to which they had acquired control of responding. When the positive color was attenuated alone or in conjunction with the negative color, angular orientation acquired control of responding in an errorless fashion. Lines, however, did not acquire control when only the negative component was attenuated. These results were interpreted in terms of changes in the predictability of reinforcement by color and line elements during stimulus attenuation. Finally, attenuation of the negative stimulus influenced the number of “dimensions” of the new line stimuli that acquired control of responding. When the positive stimulus was attenuated with the negative, only one dimension of the lines acquired control. When the positive stimulus was attenuated without the negative, however, more than one dimension of the lines acquired control of responding. These results were interpreted in terms of how errorless performance can be maintained while an organism attends to different dimensions of the new stimuli.     

Discrimination of simultaneous and successive tones

A series of discrimination tasks involving simultaneous and successive presentation of pairs of piano notes was given to 27 Ss. The listeners exhibited less-than-perfect ability to “hear out” the component notes in simultaneous presentations. This finding, in agreement with the results of previous investigators, demonstrated the limitation of Ohm’s law of acoustical analysis. It was also found that changes in successive notes fOllowing simultaneous notes were discriminated more accurately than changes in simultaneous notes following successive notes. This was interpreted as suggesting that listeners are better able to analyze than to synthesize the components of complex tones.     

Quantity discrimination in female mosquitofish

The ability in animals to count and represent different numbers of objects has received a great deal of attention in the past few decades. Cumulative evidence from comparative studies on number discriminations report obvious analogies among human babies, non-human primates and birds and are consistent with the hypothesis of two distinct and widespread mechanisms, one for counting small numbers (<4) precisely, and one for quantifying large numbers approximately. We investigated the ability to discriminate among different numerosities, in a distantly related species, the mosquitofish, by using the spontaneous choice of a gravid female to join large groups of females as protection from a sexually harassing male. In one experiment, we found that females were able to discriminate between two shoals with a 1:2 numerosity ratio (2 vs. 4, 4 vs. 8 and 8 vs. 16 fish) but failed to discriminate a 2:3 ratio (8 vs. 12 fish). In the second experiment, we studied the ability to discriminate between shoals that differed by one element; females were able to select the larger shoal when the paired numbers were 2 vs. 3 or 3 vs. 4 but not 4 vs. 5 or 5 vs. 6. Our study indicates that numerical abilities in fish are comparable with those of other non-verbal creatures studied; results are in agreement with the hypothesis of the existence of two distinct systems for quantity discrimination in vertebrates.     

A peak shift on a line-tilt continuum

Pigeons were trained to discriminate the presence or absence of a vertical line, and their performance on a subsequent generalization test was compared with that of other pigeons trained to discriminate a vertical from a 45° line. On the generalization gradient after discrimination training, the presence/absence discrimination group showed a peak at 0° (vertical) while the peak for the 0°/45° discrimination group shifted from 0° in a direction away from the 45° line. The results, discussed in connection with a recent suggestion about the role of color in the peak-shift effect, are interpreted as supporting the generality of the phenomenon.