On the role of covarying functions in stimulus class formation and transfer of function

This experiment investigated whether directly trained covarying functions are necessary for stimulus class formation and transfer of function in humans. Initial class training was designed to establish two respondent-based stimulus classes by pairing two visual stimuli with shock and two other visual stimuli with no shock. Next, two operant discrimination functions were trained to one stimulus of each putative class. The no-shock group received the same training and testing in all phases, except no stimuli were ever paired with shock. The data indicated that skin conductance response conditioning did not occur for the shock groups or for the no-shock group. Tests showed transfer of the established discriminative functions, however, only for the shock groups, indicating the formation of two stimulus classes only for those participants who received respondent class training. The results suggest that transfer of function does not depend on first covarying the stimulus class functions.     

The effects of varying the distribution of generalization stimuli within a constant range upon the bisection of a sound-intensity interval by rats

Two male, albino rats were trained on a two-valued, self-paced, discrete-trials auditory discrimination. In the presence of a high-intensity stimulus (90 decibels SPL, 4 kiloHertz), response A was reinforced; in the presence of a low-intensity stimulus (50 decibels SPL, 4 kiloHertz), response B was reinforced. When discrimination performance was asymptotic, stimuli intermediate in intensity were presented with the training stimuli in a maintained generalization paradigm. Generalization gradients were derived from the relative frequencies of response A in the presence of each stimulus. A relative frequency of 0.50 was then determined and used as the bisection point of the intensity interval defined by the 90- and 50-decibel stimuli. The bisection point varied with the distribution of the stimuli presented in generalization. This effect was similar to context effects seen in human psychophysics.     

Degree of representation of the matching concept in pigeons (Columba livia)

In Experiment 1, 12 pigeons (Columba livia) were trained on a simultaneous matching-to-sample task with 2 stimuli and then tested with 2 novel stimuli. Half of the birds were trained with a fixed ratio schedule requirement of 1 (FR1) or 20 (FR20) pecks on the sample stimulus. None of the birds showed any evidence of concept-mediated transfer. In Experiment 2, 12 pigeons were trained with 3 stimuli and then tested with the same novel stimuli used in Experiment 1. Half of the birds in each group were trained with either an FR1 or FR20 requirement on the sample stimulus. Two of the FR20 birds showed high levels of transfer to the novel stimuli similar to that of monkeys in a previous study.     

Discrimination learning as a function of stimulus location along an auditory intensity continuum

Eight groups of rats were trained on an auditory intensity discrimination in which the discriminative stimuli were separated by 10 decibels (db). Four pairs of stimuli were selected from different regions along a 60–100 db (SPL) intensity continuum. Counterpart groups were trained on each stimulus pair, with the relative intensity positions of the reinforced stimulus (S^D) and the non-reinforced stimulus (S^Δ) reversed for the two groups. Discrimination acquisition curves were compared to determine whether stimuli separated by equal logarithmic units were of comparable “difficulty”, and to determine the relative effectiveness of an S^D serving as the more versus less intense member of a stimulus pair. It was concluded that: (1) When S^D is the more intense, auditory intensities of constant logarithmic separation are graded in “difficulty” along the intensity continuum; high intensity discriminative stimuli are most readily discriminated. When S^Δ is the more intense, this graded effect is not evident. (2) For a given continuum location, discrimination is inferior when S^Δ is the more intense. This effect is most pronounced at the high intensity end of the continuum and is chiefly attributable to differences in the rate of S^Δ responding.     

Stimulus duration as a measure of stimulus generalization

Four pigeons in the line-positive group were trained with a vertical line on a green background that signalled intermittent reinforcement while a plain green field signalled extinction. Four pigeons in the line-negative group were trained with the opposite discrimination. Response to a control key terminated any trial and initiated the next trial. The birds also used the control key during generalization tests to control the durations of trials in which various line orientations were presented. These durations were summed to provide generalization gradients of stimulus duration that were positive or negative in accordance with the trained discriminations. In Experiment 2, birds from the line-positive group were tested with a procedure in which the control key was not available on some trials. This provided an independent assessment of response rates to the test stimuli. These rates were used to predict the stimulus durations obtained when the control key was available. The findings supported a general model for the prediction of response distributions among concurrent stimuli from rates observed with single stimuli.     

Visual dominance in the pigeon

In Experiment 1, three pigeons were trained to obtain grain by depressing one foot treadle in the presence of a 746-Hertz tone stimulus and by depressing a second foot treadle in the presence of a red light stimulus. Intertrial stimuli included white light and the absence of tone. The latencies to respond on auditory element trials were as fast, or faster, than on visual element trials, but pigeons always responded on the visual treadle when presented with a compound stimulus composed of the auditory and visual elements. In Experiment 2, pigeons were trained on the auditory-visual discrimination task using as trial stimuli increases in the intensity of auditory or visual intertrial stimuli. Again, pigeons showed visual dominance on subsequent compound stimulus test trials. In Experiment 3, on compound test trials, the onset of the visual stimulus was delayed relative to the onset of the auditory stimulus. Visual treadle responses generally occurred with delay intervals of less than 500 milliseconds, and auditory treadle responses generally occurred with delay intervals of greater than 500 milliseconds. The results are discussed in terms of Posner, Nissen, and Klein's (1976) theory of visual dominance in humans.     

Extending sequence-class membership with matching to sample

Three normal adults were first trained to point sequentially to each member of several pairs of visual stimuli. This baseline training established one class of stimuli to which subjects responded first, and another class of stimuli to which they responded second. Then, in a matching-to-sample procedure, baseline-sequence stimuli served as samples and new visual stimuli served as comparisons. Subjects were trained to choose one group of new comparisons when the sample was a "first" stimulus from the sequence baseline, and to choose the other new comparison stimuli when the sample was a "second" from the sequence baseline. When the new stimuli were then presented as pairs in the posttest, two subjects pointed to them in sequences predictable on the basis of the stimulus-class membership established during matching to sample. The failure of one subject to demonstrate sequential transfer was shown to be a consequence of the failure of the matching-to-sample procedure to establish stimulus classes. The production of sequences that were not directly trained suggested an empirical approach to the analysis of simple grammatical behavior.     

Generalization of Habituation and Intrinsic Sensitization in the Leech

Using the shortening reflex of the medicinal leech Hirudo medicinalis we examined stimulus generalization of habituation learning. Preparations received mechanosensory stimulus at two positions on the leech body wall, one site used to carry out habituation training and a second novel site to test for generalization of habituation. After training, the specific mechanosensory neurons activated by each stimulus were assessed using intracellular recordings. As expected, the closer the two sites were to each other, the greater the degree of generalization of habituation at the novel site and the more sensory cells were shared. However, a form of behavioral facilitation was observed at the trained site that resembled behavioral sensitization, but differed from the standard sensitization process in several respects. (1) Facilitation was induced by stimulation of the novel site before habituation training at the trained site, although the stimulus intensity at the novel site was equivalent to the training stimuli and was not the strong, noxious stimuli that normally induce sensitization. (2) The magnitude of the facilitating effect was proportional to the proximity of the novel and trained stimulation sites. (3) Although behavior at the trained site was facilitated, behavior at the novel site was habituated, indicating that the induced behavioral facilitation did not generalize throughout the animal, as normally occurs during sensitization, but was limited to a single stimulus–response pathway.     

Assessment of the relative importance of S+ and S− in rats using differential training on intercurrent discriminations

The present studies assessed the degree of stimulus control exerted by S+ and S? without confoundings of stimulus novelty and stimulus ambiguity. In Experiment 1, rats were trained on two intercurrent simultaneous discrimination problems with nine times more training given on one than the other. Then the animals were given transfer tests with re-paired stimuli. The results showed that S? exerts greater stimulus control than S+ in a two-choice simultaneous discrimination. Experiment 2 provided a test of the possibility that the relative degree of control by S? varies with different amounts of training. Three groups were trained on two intercurrent simultaneous discrimination problems; each group was given 7, 11, or 15 times more training on one problem than the other. Then transfer tests were given with re-paired stimuli. Again the results showed that S? exerts greater stimulus control than S+ in a two-choice simultaneous discrimination.     

Self-instructions as discriminative cues for rule-breaking or rule-following

This experiment examined the relationship between self-instructions and subsequent instruction-following performance, as a function of the history of the consequences for correspondence or noncorrespondence. Subjects were two groups of elementary school children (ages 7 and 8 years). In training, the two groups were exposed to different histories of congruence or noncongruence between self-instructions and consequences for performance. In the Congruent group, subjects were exposed to a series of stimuli to which they were trained to give self-instructions to make, or not to make, a key-pressing response. Reinforcement was given for self-instructing, and responding in accord with the self-instruction. Subjects in the Noncongruent group were trained to give the same self-instructions for the same stimuli, but reinforcement was given for counter-compliance. Subsequently, in a temptation situation, the experimenter gave an instruction not to press for a test stimulus; and subjects were trained to give the inhibitory self-instruction for this stimulus. Subjects in the Noncongruent group showed a high rate of rule-breaking. The effects on behavior of self-delivered instructions depend on the past relations between these events and the consequences for instruction-following. Implications are discussed for moral behavior and cognitively oriented therapy.     

Stimulus factors in the training of prepositional usage in three autistic children

Language deficient, autistic children were trained to use the prepositions "in" and "on". Three subjects were exposed to conditions of training that differed in the method of employment of stimulus objects used to train prepositional usage. Two subjects were trained first with "ambiguous" stimuli, that is, the same stimulus objects were used for training both prepositions. The two subjects were then switched to a training condition with "non-ambiguous" stimulus objects, that is, objects used for training "in" were different than those used for training "on". The two subjects were then switched to the ambiguous stimulus condition and finally returned again to training with non-ambiguous stimuli (four conditions). A third subject began with training on non-ambiguous stimuli, was switched to an ambiguous condition and was then switched back to non-ambiguous stimuli (three conditions). The results for two of the three subjects indicated that accurate usage of the two prepositions was obtained only under training conditions with non-ambiguous stimuli. Results for the third subject suggested that initial training with non-ambiguous stimuli might enhance subsequent accurate responding with ambiguous stimuli.     

Blocking the development of stimulus control when stimuli indicate periods of nonreinforcement

To learn whether prior discrimination training based on one stimulus would block learning about a subsequently added stimulus, rats were first trained to press a bar on a variable-interval schedule of food reinforcement. Occasional stimuli were presented during which no reinforcement was available. Responding became suppressed in the presence of these stimuli. Stimuli could be noise, light, or a compound of noise plus light. A group trained with noise in Phase 1, then trained with the compound in Phase 2, showed less suppression to light in a subsequent test than a group that had the same compound training in Phase 2 but only variable-interval training in Phase 1. This showed that prior training with noise blocked the development of control by light during compound training. Two further groups showed that noise training following compound training did not have the same effect on control by light.     

Peak shift revisited: a test of alternative interpretations

In Experiment 1, 2 groups of human subjects were trained to respond to 1 of 2 light intensity stimuli, S2 or S4, and then were tested for generalization with a randomized series of increasing values from S1 to S11. Both groups, including the group trained to respond to dimmer value, showed peak shifts to a brighter more centrally located test stimulus. In Experiment 2, which used line angle stimuli, both the size of the difference between S+ and S- and the range of test stimuli that extended beyond S+ were varied. The larger the S(+)-S- separation and the larger the range, the greater was the peak shift obtained. In Experiment 3, training involved an S- (line angle) surrounded by 2 S+ values with testing symmetrical about the training values and covering either a narrow or a wide range. The wide range produced greater peak shifts in both directions from S-. All 3 experiments support an adaptation-level interpretation of intradimensional discrimination learning and generalization test performance in human subjects. Related work with animals suggests the presence of similar processes.     

On the effectiveness of including meaningful pictures in the formation of equivalence classes

In three experiments, 165 adult participants were trained on 12 baseline conditional discriminations and tested for the formation of three 5-member equivalence classes (A➔B➔C➔D➔E). All experiments included two reference groups; the abstract (ABS) group was trained with all abstract stimuli and the picture (PIC) group with C-stimuli as meaningful pictorial stimuli but A, B, D, and E stimuli as abstract shapes. In Experiment 1, the color of the meaningful stimuli was manipulated. In the ABS, PIC, and black-and-white groups, 33.3%, 80%, and 93.3% formed equivalence classes, respectively. In Experiment 2, participants were exposed to a test block with and without trials that included C stimuli. For the groups with and without C trials in the test, 93.3% and 86.7% formed equivalence classes, respectively, compared to 20% in the ABS group. In Experiment 3, the number of meaningful pictures and their location in stimulus classes were manipulated. One group was trained with 3 pictures (C1/B2/D3, the 3-PIC) while the other groups had 2 pictures (C1/B2 and C1/D3, the 2-PIC). In the second test block for the ABS and PIC groups, 6.7% and 86% of the participants formed equivalence classes, respectively. For the 3-PIC and the 2-PIC groups, 66.7% and 50% of the participants formed equivalence classes, respectively. Results suggest that the effects of meaningful stimuli in equivalence classes (a) cannot be attributed to the use of colorful stimuli in previous studies, (b) occur during training and are not dependent on the presence of meaningful stimuli at test, and (c) are sensitive to stimulus location.     

Naming and equivalence: Response latencies for emergent relations

In an attempt to distinguish between associative network and verbal mediation accounts of equivalence formation, three experiments were carried out in which conditional stimulus relations were established and response latencies assessed during tests for emergent relations. In Experiment 1, three groups of adults were trained with six three-member classes of visual stimuli, using different kinds of stimuli for each group: readily nameable pictograms, which were “preassociated” (Group 1); equally nameable but “non-associated” pictograms (Group 2); or non-associated “abstract” stimuli, designed to discourage the use of verbal mediators (Group 3). For those trained with pictograms, equal response latencies were observed on all tested relations, viz. trained associations, symmetry, transitivity, and transitivity with symmetry, but for subjects given abstract stimuli response latencies were greater on tests requiring transitivity. In Experiment 2 this result was replicated with methodological refinements, using only groups trained with preassociated pictograms or abstract stimuli. In Experiment 3 subjects were pretrained to label abstract stimuli with either individual names or class names. Latencies were longer for tests involving transitivity in the case of those subjects using individual names, but equal response latencies were observed on all four types of test for those using class names. The results suggest that equivalence classesMaybe supported by either an associative network or by verbal mediation, depending on stimulus conditions and the subsequent strategies employed by subjects.     

Taking a bright view of negative priming in the light of dim stimuli: further evidence for memory confusion during episodic retrieval.

A same-different letter-matching task was used to examine the effects of stimulus intensity on negative priming, which is poorer performance when target letters have been presented as distractor letters on the immediately preceding trial. In Experiment 1, stimulus intensity was manipulated between-participants, whereas in Experiment 2, it varied randomly from trial-to-trial within-participants. In Experiment 1, negative priming was equivalent for both stimulus intensities. In Experiment 2, negative priming effects were larger for repeated intensity stimuli than for nonrepeated intensity stimuli, when stimulus intensity was dim. Furthermore, for repeated intensity stimuli, negative priming effects were enhanced when the overt response required to the stimulus was repeated from prime to probe trial. These results are consistent with the hypothesis that negative priming may be due to memory confusion, rather than to inhibition of the distractor stimuli.     

The influence of stimulus properties on multisensory processing in the awake primate superior colliculus.

Multisensory integration is a process whereby information converges from different sensory modalities to produce a response that is different from that elicited by the individual modalities presented alone. A neural basis for multisensory integration has been identified within a variety of brain regions, but the most thoroughly examined model has been that of the superior colliculus (SC). Multisensory processing in the SC of anaesthetized animals has been shown to be dependent on the physical parameters of the individual stimuli presented (e.g., intensity, direction, velocity) as well as their spatial relationship. However, it is unknown whether these stimulus features are important, or evident, in the awake behaving animal. To address this question, we evaluated the influence of physical properties of sensory stimuli (visual intensity, direction, and velocity; auditory intensity and location) on sensory activity and multisensory integration of SC neurons in awake, behaving primates. Monkeys were trained to fixate a central visual fixation point while visual and/or auditory stimuli were presented in the periphery. Visual stimuli were always presented within the contralateral receptive field of the neuron whereas auditory stimuli were presented at either ipsi- or contralateral locations. Many of the SC neurons responsive to these sensory stimuli (n = 66/84; 76%) had stronger responses when the visual and auditory stimuli were combined at contralateral locations than when the auditory stimulus was located on the ipsilateral side. This trend was significant across the population of auditory-responsive neurons. In addition, some SC neurons (n = 31) were presented a battery of tests in which the quality of one stimulus of a pair was systematically manipulated. A small proportion of these neurons (n = 8/31; 26%) showed preferential responses to stimuli with specific physical properties, and these preferences were not significantly altered when multisensory stimulus combinations were presented. These data demonstrate that multisensory processing in the awake behaving primate is influenced by the spatial congruency of the stimuli as well as their individual physical properties.     

The nature of control by spoken words over visual stimulus selection.

Eight retarded adolescents were trained to select one (a trained S+) of two visual stimuli in response to a spoken word (a trained word). Two different visual stimuli alternated randomly as the S-. To determine if the spoken work was merely a temporal discriminative stimulus for when to respond, or if it also specified which visual stimulus to select, the subjects were given intermittent presentations of untrained (novel) spoken words. All subjects consistently selected the trained S+ in response to the trained spoken word and selected the previous S- in response to the untrained spoken words. It was hypothesized that the subjects were responding away from the trained S+ in response to untrained spoken words, and control by untrained spoken words would not be observed when the trained S+ was not present. The two visual S- stimuli selected on trials of untrained spoken words were presented simultaneously. The untrained spoken words presented on these trials no longer controlled stimulus selections for seven subjects. The results supported the hypothesis that previous control by spoken words was due to responding away from the trained S+ in response to untrained spoken words.     

Negative patterning is easier than a biconditional discrimination

Two groups of rats were trained for 50 days on different discriminations in a magazine approach paradigm. One group was trained with a negative patterning schedule and a positive patterning schedule concurrently: they received intermixed trials of A+, B+, AB-, C-, D-, CD+ (A, B, C, and D are four distinct stimuli; the plus sign denotes reinforcement with food, and the minus sign denotes nonreinforcement). The second group of rats was trained with the same four stimuli arranged as compounds and reinforced according to the biconditional schedule AB+, CD+, AC-, and BD-. The first group learned the positive patterning schedule much more quickly than the negative patterning schedule, but they learned the negative patterning schedule more effectively than the second group learned the biconditional schedule. The authors discuss the implications of these findings for models of stimulus representation.