Serial discrimination reversal learning in pigeons as a function of intertrial interval and delay of reinforcement

Pigeons learned a series of reversals of a simultaneous red-green visual discrimination. Delay of reinforcement (0 vs. 2 sec) and intertrial interval (ITI; 4 vs. 40 sec) were varied across blocks of reversals. Learning was faster with 0-sec than with 2-sec delays for both ITI values and faster with 4-sec ITIs than with 40-sec ITIs for both delays. Improvement in learning across successive reversals was evident throughout the experiment, furthermore, even after more than 120 reversals. The potent effects of small differences in reinforcement delay provide evidence for associative accounts and appear to be incompatible with accounts of choice that attempt to encompass the effects of temporal parameters in terms of animals’ timing of temporal intervals.     

Systematic errors in pigeons’ memory for event duration: Interaction between training and test delay

Pigeons trained to choose different stimuli following short- and long-duration signals make disproportionately more “short” choices (i.e., “choose-short errors”) following an increase in the retention interval and more “choose-long errors” following a decrease in this delay. The present experiment provided a systematic investigation of how these selective errors depend on the relationship between the training delay and the test delay. Pigeons were first trained with a 0-sec delay between the signal (2- or 8-sec food presentations) and the choice stimuli (red- and blue-lit keys). On subsequent test trials with 5- and 10-sec delays, choose-short errors predominated. Next, the birds were trained with a constant 10-sec delay and then tested with shorter or longer delays on some trials. The birds now responded accurately and without selective errors at the 10-sec training delay, but made choose-long errors at shorter delays and choose-short errors at longer delays. Finally, the birds were trained with a constant 20-sec delay and then tested with shorter and longer delays. Choose-long errors again appeared at shorter test delays, choose-short errors at longer test delays, and no differential errors at the 20-sec training delay. The selectivity of these errors generally increased with the absolute difference between the training and test delay. Theoretical implications of these results are discussed.     

Two-choice conditional discrimination performance of pigeons as a function of reward expectancy,prechoice delay,and domesticity

In a discrete-trial two-choice conditional discrimination task, pigeons which received food for a correct choice following the presentation of one cue and water for a correct choice following another cue performed better than pigeons which received food and water equally often in both cases when delays of several seconds intervened between the conditional cue and choice stimuli presentations. These results suggest that feedback properties of reinforcer-specific expectancies can be important in conditional discrimination learning in pigeons. An additional finding was that wild-caught pigeons regularly exhibited a higher percentage of correct choices than domestic subjects.     

Domestic pigeons (Columba livia) discriminate between photographs of male and female pigeons

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.     

Prospective and retrospective timing by pigeons

Pigeons discriminated between two pairs of durations: a short set (2.5 and 5 sec) and a long set (5 and 10 sec). The pairs were intermixed within sessions and identified by the colors on the signal and choice keys. Once the task was learned, the pigeons experienced the following three conditions seriatim: (1) The signal key was made ambiguous about the test change, but the choice keys were informative (retrospective); (2) the signal key identified the test range, but the choice keys did not (prospective); (3) probe trials were introduced in which the color of the center key signaled one test range, but the color of the choice keys signaled the other test range (inconsistent). Accuracy of choice decreased in the retrospective condition and, returned to baseline levels, was higher under the prospective condition than under the retrospective condition. In a final condition, referred to as conflict trials, the center-key color signified one test range and the choice-key colors the other range. The results from these conflict-inconsistent tests indicate that choice behavior was largely controlled by the signal-key color and not by the choice-key color. We relate these findings to different approaches to timing in animals.     

Form perception and attention in pigeons

This report selectively reviews the authors’ research on stimulus control by visual forms. Most studies employed visual search of computer-generated displays, and the main behavioral measure was search reaction time. Pigeons classify simple line forms much as do humans, and there was some evidence for feature extraction, though a search asymmetry probe failed to identify several putative features. Dimensional analysis revealed a new quantitative relation between similarity and the probability of detecting a target. It also identified candidates for integral and separable stimulus dimensions. Similarity and set-size variables influenced the extent to which attention was engaged. Further studies addressed the manner in which attention is focused, revealing relationships between priming and search images. In these cases, attention to a selected form is probably driven by a top-down assessment of predictability.     

Choice and percentage reinforcement in pigeons

Pigeons responded on a two-key concurrent chains choice procedure with the same level of percentage reinforcement on each key. During the initial links, a choice response on either key occasionally produced a conditioned reinforcer—which on one key was associated with a 15-sec, and on the other key with a 30-sec, interreinforcement interval—or an extinction stimulus. In Part 1, the initial links were equal. With successive decreases in the probability of a reinforcer, choice shifted from preference for the 15-sec terminal link toward indifference. In Part 2, the initial links were unequal and were arranged so that the shorter initial link preceded the 30-sec terminal link. At a high probability of a reinforcer, the pigeons again preferred the 15-sec terminal link. However, at a low probability, the pigeons reversed and preferred the alternate key. It was concluded that the conditioned reinforcers tended to become functionally equivalent at a low probability of a reinforcer, despite the nominally different interreinforcement intervals, with the result that choice was then modulated by the relative size of the initial links. The data are inconsistent with the view that choice and the strength of conditioned reinforcers are isomorphic with the reduction in delay to reward correlated with terminal link stimuli.     

Controlled processing in pigeons

This paper investigates whether rehearsal, or posttrial processing, of information about an event can be modulated by instructions in infrahuman organisms. Using pigeons, a procedure was developed for establishing a stimulus as a cue to disengage rehearsal, or posttrial processing, of a food reinforcer. Specifically, the stimulus instructed the animals to behave on a subsequent choice test as if food had not, in fact, been presented. Results are reported that suggest that this training was successful in establishing the stimulus as a cue to forget the occurrence of the food. These findings are interpreted as providing tentative support for the view that the cognitive repertoire of infrahuman organisms does include controlled processing strategies.     

Transverse patterning in pigeons

Pigeons were trained to choose between colored lights (A, B, C, and D), first in a two-pair ambiguouscue problem (A+B?, B+C?), and then, with all colors nondifferentially reinforced, in a three-pair loop problem (A+B?, B+C?, C+A?) followed by a four-pair loop problem (A+B?, B+D?, D+C?, C+A?). Systematic efforts were made to simulate the data with a variety of models incorporating one or another of three conceptions of stimulus compounding prominent in the literature on compound conditioning. One conception is that the components of a compound stimulus are altered by interaction; the second is that they are not altered, but only supplemented with a new (compound-unique) component generated in the interaction; and the third is that the components entirely disappear in a configurational transformation. The ambiguous-cue data could be simulated accurately with each of the models, but the loop data with none of them. A convincing explanation of performance in loop problems remains to be found.     

Attempts to demonstrate magnetic discrimination by homing pigeons in flight

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.     

Children's Sensitivity to Lack of Understanding

Successful tutoring depends in part on child tutors’ ability to recognise and interpret accurately signals of misunderstanding by their tutees. Age- and gender-related differences were investigated in a study which exposed 80 children to a video-recorded episode involving a target child receiving ambiguous instructions in her attempts to move a model car along a designated route on a playmat roadway from one destination to another. The results showed that explicit, general and facial modes of displaying puzzlement by the target child were judged as equally powerful expressions of degree of puzzlement, but 8-10 year olds judged the target child as significantly more puzzled than did 7 year olds. Older children were also more likely to attribute the puzzlement of the target child to the ambiguous instructions than to her verbal or facial expression of puzzlement. Girls were generally more accurate than boys in judging facial expressions and less likely than boys to give wrong or alternatively ambiguous responses when given the opportunity to correct the video-recorded ambiguous instructions. The results throw some light on the developing sensitivities of boys and girls in recognising and attributing failures of understanding by other children.     

Toddlers' Sensitivity to Standard Violations

Young children's emerging sensitivity to standard violations has been postulated, but not systematically examined, as an important aspect of early morality. In this study, we observed 100 26–41-month-old toddlers in contexts that involved standard violations. In one context, children were shown flawed and whole objects. In the other context, they were led to believe they had damaged the examiners' valued possessions ("mishaps"). When presented with the flawed and whole objects, toddlers expressed preference for the latter, but showed more interest in the former, thus indicating that the whole-flawed quality was salient. Verbal and nonverbal reactions reflecting sensitivity to the whole-flawed aspects were interrelated. Moreover, manifestations of sensitivity to flawed objects were associated with several behavioral and affective responses during the contrived mishaps (acceptance of responsibility, apologies, focus on reparations, and distress). Thus, sensitivity to standard violations in toddlerhood appeared to be a general phenomenon underlying different aspects of early morality.     

Categorical discrimination of objects and pictures by pigeons

With a three-choice instrumental discrimination procedure, pigeons were taught to distinguish small spherical objects from nonspherical objects. Spherical objects were defined as positive, nonspherical objects as negative. A device allowing an automatic presentation of the stimuli was employed. The subjects actually pecked the objects, and grain rewards were presented directly beside the correct objects. Acquisition was rapid, with the birds reaching a criterion of 80% correct choices within less than 150 trials. There was evidence that more than 200 objects were remembered individually over 3 months. Pigeons transferred the discrimination of spherical/nonspherical objects to novel objects. The criteria by which the birds judged the sphericity of objects seemed to be similar to those applied by humans. They could apply the categorization in a relational manner and generalize it to apply to photographs and drawings of objects. The categorization competence was retained for at least 3 months.     

Blocking of first- and second-order autoshaping in pigeons

In Experiment 1, the development of autoshaped pecking to a keylight signaling food was blocked if the keylight was presented only in conjunction with another stimulus already established as a signal for food, even though the blocking stimulus (either an overhead light or a train of clicks) never elicited pecking itself. In Experiment 2, pigeons came to peck a white keylight which signaled the presentation of a red keylight which had earlier been established as a first-order signal for food, but this second-order autoshaping was blocked if the white keylight was presented only in conjunction with the houselight or clicker which had previously signaled the presentation of the first-order stimulus. Second-order autoshaping was thus blocked in the same way as was first-order autoshaping.     

Sensitivity and Security: New Questions to Ponder

The conclusion that parental sensitivity is a reliable—but not highly robust—predictor of a secure attachment invites reconsideration of the nature of sensitivity and its impact on early psychosocial development. Future directions for inquiry include (1) renewed attention to the growth of attachment in the context of other developing features of the parent-infant relationship, including play and behavioral management; (2) the factors that moderate the impact of sensitivity on developing security (including the contexts of sensitive responsiveness infant age, and the consistency of parental sensitivity over time); (3) the multifaceted and dyanamic origins of individual differences in sensitivity; and (4) greater consideration of why sensitivity fosters attachment security, especially in relation to emergent working models of relationships and self.     

The role of test stimuli in matching to compound samples by pigeons

Two pigeons matched to sample in a three-key operant conditioning chamber. In Experiment I, two different kinds of samples were presented on the center key.Element samples were members of one of two sample sets — colors (a red or blue disk) or lines (a vertical or horizontal orientation of a set of white lines). These samples were followed by their respective sample sets on the side keys as comparison stimuli.Compound samples consisted of a set of lines superimposed on a colored disk. Following these samples, either sample set could appear as comparison stimuli. Matching to compound samples was less accurate than matching to element samples. One interpretation is that sharing of attention among elements of a compound sample weakened stimulus control by each element. A different interpretation is that an element sample controlled matching better because it was physically identical to a comparison stimulus whereas a compound sample was not. Experiments II–IV evaluated this “generalization decrement” alternative by testing element- vs. compound sample control with both element and compound comparison stimuli. Irrelevant elements were added to form compound comparison stimuli, some of which were physically identical to a preceding compound sample, but never identical to an element sample. In all experiments, the addition of irrelevant elements of comparison stimuli reduced sample control. However, the generalization decrement hypothesis failed to predict how differences in performance maintained by element and compound samples were affected by different tests of sample control. Matching accuracy appeared to be independently determined by the number of elements in a sample and whether irrelevant elements were present during tests of sample control.     

Recall of three-item sequences by pigeons

Pigeons were trained to recall an arbitrary sequence on a delayed matching-to-successive-samples (DMTSS) task. Sample items were presented successively and then displayed simultaneously. Subjects were required to respond to them in the order in which they appeared. In Experiment 1, pigeons responded correctly on 75% of the trials on a two-item DMTSS task but at a chance level of accuracy on a three-item task. In Experiment 2, pigeons who learned to produce a three-item sequence prior to DMTSS training mastered a three-item DMTSS task at a 75% level of accuracy. Control groups, trained initially with the same items on nonserial tasks, performed as poorly on a three-item DMTSS task as the naive subjects of Experiment 1. It was hypothesized that pigeons that first learned to produce a three-item list were able to recall three-item samples in DMTSS because they had learned to represent three-item sequences.     

Cross-stimulus transfer of timing in pigeons

Pigeons were trained in a delayed matching task in which the samples were short (2 sec) and long (10 sec) presentations of either a houselight or a keylight. Transfer trials involved short and long presentations of the nontrained signal as the sample. In the intermittent transfer test, infrequent transfer trials were intermixed with more frequent training trials; in the sustained transfer test, all trials were transfer trials. The intermittent test revealed only weak transfer. The sustained test revealed transfer in Session 1 only in birds that had received pairings of the transfer signal and food prior to testing. However, regardless of whether the transfer signal had been previously paired with food, birds exposed to consistent contingencies between duration and choice across training and testing learned the transfer task more rapidly than did birds exposed to inconsistent contingencies. It was concluded that some training in which the transfer signal serves as the sample is required before the durations of a transfer signal are related to the rules associating duration and responding     

Discrimination of relative numerosity by pigeons

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.     

Artificial grammar learning in pigeons

In two experiments, we developed a new methodology for studying complex stimulus control by spatial sequences of letters generated by artificial grammars. An artificial grammar is a system of rules that defines which letter sequences or strings are “grammatical.” In Experiment 1, pigeons learned to respond differently to strings conforming to a grammar versus strings that were nongrammatical distortions. Several different criteria all suggested that performance was controlled both by some short chunks of strings shared between reinforced training strings and novel transfer strings and by more complex sequential regularities. In Experiment 2, pigeons quickly and accurately learned to respond differently to strings conforming to one or the other of two different artificial grammars. As in Experiment 1, performance was controlled both by some short chunks and by more complex sequential regularities. The results are interpreted in terms of family resemblance and pose new goals for theories of complex stimulus control.