Reflections on stimulus control

The topic of stimulus control is too broad and complex to be traceable here. It would probably take a two-semester course to cover just the highlights of that field's evolution. The more restricted topic of equivalence relations has itself become so broad that even an introductory summary requires more time than we have available. An examination of relations between equivalence and the more general topic of stimulus control, however, may reveal characteristics of both the larger and the more limited field that have not been generally discussed. Consideration of these features may in turn foster future developments within each area. I speak, of course, about aspects of stimulus control that my own experiences have made salient to me; others would surely emphasize different characteristics of the field. It is my hope that cooperative interactions among researchers and theorists who approach stimulus control from different directions will become more common than is currently typical.     

On Stimulus Generalization and Stimulus Classes

Stimulus generalization has been defined as the spread of effect of reinforcement for responses emitted in the presence of one stimulus to different stimuli presented under extinction conditions. As a result of stimulus generalization, novel stimuli come to exert stimulus control over members of the response class. Studies in the applied behavior analysis literature, however, have reported experimental preparations that included prompting and reinforcement procedures during what were claimed to be stimulus generalization conditions. These studies violated the procedural requirement that stimulus generalization be tested under extinction conditions. Responses that come under the control of a class of stimuli may do so by direct training or by stimulus generalization. It is desirable for organisms to respond in the presence of members of an appropriately constructed stimulus class, but we should understand the mechanism of entry into the class by its members. If inaccurate claims of stimulus generalization are made when training procedures are used in the ostensible generalization conditions, the robustness of the original training procedures will be over estimated. By adhering to the operational requirements of behavioral definitions, we could better understand the power and limits of our educational and training procedures.     

Compound stimuli in emergent stimulus relations: Extending the scope of stimulus equivalence

Three experiments were conducted to investigate stimulus relations that might emerge when college students are taught relations between compound sample stimuli and unitary comparison stimuli using match-to-sample procedures. In Experiment 1, subjects were taught nine AB-C stimulus relations, then tested for the emergence of 18 AC-B and BC-A relations. All subjects showed the emergence of all tested relations. Twelve subjects participated in Experiment 2. Six subjects were taught nine AB-C relations and were then tested for symmetrical (C-AB) relations. Six subjects were taught nine AB-C and three C-D relations and were then tested for nine AB-D (transitive) relations. Five of 6 subjects demonstrated the emergence of symmetrical relations, and 6 subjects showed the emergence of transitivity. In Experiment 3, 5 college students were taught nine AB-C and three C-D relations and were then tested for nine equivalence (D-AB) relations and 18 AD-B and BD-A relations. Three subjects demonstrated all tested relations. One subject demonstrated the AD-B and BD-A relations but not the D-AB relations. One subject did not respond systematically during testing. The results of these experiments extend stimulus equivalence research to more complex cases.     

A test of symmetry and transitivity in the conditional discrimination performances of pigeons

In a matching-to-sample context, pigeons were taught two conditional discriminations according to one of three equivalence paradigms: train if A, then select B and if B, then select C; train if B, then A and if B, then C; or train if A, then B and if C, then B. Test trials without reinforcement revealed that the conditional relations did not satisfy the symmetrical and transitive properties of an equivalence relation. Apparently, only specific if... then relations were learned. Contrary to Kendall's (1983) findings, and probably as a consequence of procedural differences, none of the pigeons in the present experiment were observed to emit mediating behavior during the transitivity probe trials. The absence of symmetry and transitivity may be related to the individual stimuli not being reflexive. Behavioral techniques other than the commonly used matching-to-sample technique might better succeed in avoiding unintended stimulus control in the study of the formation of stimulus classes.     

The development of derived stimulus relations through training in arbitrary-matching sequences

Five-year-old children were taught three-stage sequences of arbitrary matching: A-C, B-C, A-D; A-C, B-D, B-C; or A-C, A-D, B-C. Each stage refers to a sample-comparison relation between stimuli. Unreinforced test probes revealed untrained arbitrary matches (B-D, A-D, and B-D, respectively), derivable by substitution of stimuli with a common sample or comparison function. Additional probes revealed further untrained sample-comparison relations derivable by substitution and identity, including the commuted relations D-B, D-A, and D-B, respectively. These processes may have relevance to conceptual and verbal behavior.     

The perception of self-motion induced by central and peripheral visual stimuli moving in opposite directions

The effects of the size of a stimulus and its eccentricity (central or peripheral) on the visually induced perception of horizontal translational self-motion (vection) were investigated. The central and peripheral areas of the observers' visual field were simultaneously stimulated by random dot patterns that moved in opposite directions. The results of two experiments indicated that the effects of central and peripheral presentations of the moving visual pattern are equivalent, and that vection strength is determined by the stimulus size and speed but not by its eccentricity. These results are consistent with the findings of previous studies that suggested that there are no qualitative differences in the vection-inducing potentials of the central and peripheral areas of the visual field, and are counter to the more traditional hypothesis, which has assumed that the perception of self-motion is specifically assigned to peripheral vision.     

刺激类型及表征关系对无意视盲的影响

通过考察刺激类型以及重叠呈现的图片流和词语流的表征关系对非注意刺激的捕获差异,试图考察刺激类型和表征关系对无意视盲（Inattentional Blindness）的影响。分别有20名中学生参加了词和图片基线水平测试,52名中学生参与了无意视盲实验。研究结果表明：（1）当词与图片重叠呈现时,不管注意刺激是词还是图片,也不管词与图片的表征是否一致,与基线水平相比,被试都出现了显著的无意视盲现象。（2）当词与图片的表征意义一致时,如果注意刺激是图片,而非注意刺激是词,那么被试更容易觉察到非注意刺激。（3）非注意刺激与注意刺激表征意义一致时更容易捕获观察者的注意     

A discrimination analysis of training-structure effects on stimulus equivalence outcomes.

Experiments designed to establish stimulus equivalence classes frequently produce differential outcomes that may be attributable to training structure, defined as the order and arrangement of baseline conditional discrimination training trials. Several possible explanations for these differences have been suggested. Here we develop a hypothesis based on an analysis of the simple simultaneous and successive discriminations embedded in conditional discrimination training and testing within each of the training structures that are typically used in stimulus equivalence experiments. Our analysis shows that only the comparison-as-node (many-to-one) structure presents all the simple discriminations in training that are subsequently required for consistently positive outcomes on all tests for the properties of equivalence. The sample-as-node (one-to-many) training structure does not present all the simple discriminations required for positive outcomes on either the symmetry or combined transitivity and symmetry (equivalence) tests. The linear-series training structure presents all the simple discriminations required for consistently positive outcomes on tests for symmetry, but not for symmetry and transitivity combined (equivalence) or transitivity alone. Further, the difference in the number of simple discriminations presented in comparison-as-node training versus the other training structures is larger when the intended class size is greater than three or the number of classes is larger than two. We discuss the relevance of this analysis to interpretations of stimulus equivalence research, as well as some methodological and theoretical implications.     

Nodality effects during equivalence class formation: An extension to sight-word reading and concept development

Three students with moderate disabilities were taught to read and match-to-sample sight words comprising stimulus sets based upon the four food groups. We taught students conditional discriminations within four four-member sets using a single-sample/four-comparison procedure. Students were taught A-B, B-C, and C-D conditional discriminations for each of the four potential stimulus classes. Subsequent probes tested for relations based upon symmetry and one-node and two-node transitivity. The performances for all students indicated that symmetric relations emerged before one-node transitive relations, and that one-node transitive relations emerged before two-node transitive relations. These results are consistent with a pattern of responding, referred to as a "nodality effect," in which relations with fewer nodes are demonstrated prior to the demonstration of relations with a greater number of nodes. These results extend this area of research to sight-word reading for students with moderate disabilities.     

Symmetry and stimulus class formation in humans: Control by temporal location in a successive matching task

Symmetry refers to the observation that subjects will derive B‐A (e.g., in the presence of B, select A) after being trained on A‐B (e.g., in the presence of A, select B). Whereas symmetry is readily shown in humans, it has been difficult to demonstrate in nonhuman animals. This difficulty, at least in pigeons, may result from responding to specific stimulus properties that change when sample and comparison stimuli switch roles between training and testing. In three experiments with humans, we investigated to what extent human responding is influenced by the temporal location of stimuli using a successive matching‐to‐sample procedure. Our results indicate that temporal location does not spontaneously control responding in humans, although it does in pigeons. Therefore, the number of functional stimuli that humans respond to in this procedure may be half of the number of functional stimuli that the pigeons respond to. In a fourth experiment, we tested this assumption by doubling the number of functional stimuli controlling responding in human participants in an attempt to make the test more comparable to symmetry tests with pigeons. Here, we found that humans responded according to indirect class formation in the same manner as pigeons do. In sum, our results indicate that functional symmetry is readily observed in humans, even in cases where the temporal features of the stimuli prevent functional symmetry in pigeons. We argue that this difference in behavior between the two species does not necessarily reflect a difference in capacity to show functional symmetry between both species, but could also reflect a difference in the functional stimuli each species responds to.     

Control of adolescents' arbitrary matching-to-sample by positive and negative stimulus relations.

In Experiment 1, four developmentally delayed adolescents were taught an A-B matching-to-sample task with nonidentical stimuli: given Sample A1, select Comparison B1; given A2, select B2. During nonreinforced test trials, appropriate matching occurred when B stimuli appeared as samples and A stimuli as comparisons, i.e., the sample and comparison functions were symmetrical (B-A matching). During A-B or B-A matching test trials in which familiar samples and correct comparisons were presented along with novel comparisons, the subjects selected the correct comparisons. In tests with familiar samples and both incorrect and novel comparisons, subjects selected the novel comparisons, demonstrating control by both positive ("matching") and negative ("nonmatching") stimulus relations in A-B and B-A arrays. In Experiment 2, 12 developmentally delayed subjects were taught a two-stage arbitrary-matching task (e.g., A-B, C-B matching). Test sessions showed sample-comparison symmetry (e.g., B-A, B-C matching) and derived sample-comparison relations (e.g., A-C, C-A matching) for 11 subjects. These subjects also demonstrated control by positive and negative stimulus relations in the derived relations.     

Generalization of a tactile stimulus in horses.

Using horses, we investigated the control of operant behavior by a tactile stimulus (the training stimulus) and the generalization of behavior to six other similar test stimuli. In a stall, the experimenters mounted a response panel in the doorway. Located on this panel were a response lever and a grain dispenser. The experimenters secured a tactile-stimulus belt to the horse's back. The stimulus belt was constructed by mounting seven solenoids along a piece of burlap in a manner that allowed each to provide the delivery of a tactile stimulus, a repetitive light tapping, at different locations (spaced 10.0 cm apart) along the horse's back. Two preliminary steps were necessary before generalization testing: training a measurable response (lip pressing) and training on several reinforcement schedules in the presence of a training stimulus (tapping by one of the solenoids). We then gave each horse two generalization test sessions. Results indicated that the horses' behavior was effectively controlled by the training stimulus. Horses made the greatest number of responses to the training stimulus, and the tendency to respond to the other test stimuli diminished as the stimuli became farther away from the training stimulus. These findings are discussed in the context of behavioral principles and their relevance to the training of horses.     

Contextual control of stimulus generalization and stimulus equivalence in hierarchical categorization

The purpose of this study was to determine whether hierarchical categorization would result from a combination of contextually controlled conditional discrimination training, stimulus generalization, and stimulus equivalence. First, differential selection responses to a specific stimulus feature were brought under contextual control. This contextual control was hierarchical in that stimuli at the top of the hierarchy all evoked one response, whereas those at the bottom each evoked different responses. The evocative functions of these stimuli generalized in predictable ways along a dimension of physical similarity. Then, these functions were indirectly acquired by a set of nonsense syllables that were related via transitivity relations to the originally trained stimuli. These nonsense syllables effectively served as names for the different stimulus classes within each level of the hierarchy.     

双关图作为面孔刺激与非面孔刺激对大脑事件相关电位的影响

用线条描绘的图形作为刺激材料,A为老鼠,C为老头,B为双关图(ambi-guous figure)。图形按两种顺序:A→B→C(Ⅰ)和C←B→A(Ⅱ)向被试呈现,每次呈现时间100ms。被试按刺激呈现方式分成两组,每组20人。被试接受图形的同时记录事件相关电位(ERPs),B图呈现后要求被试报告观察内容。对主观报告考验,发现双关图在Ⅰ呈现方式中作为非面孔刺激(老鼠)被认知,在Ⅱ呈现方式中作为面孔刺激(老头)被认知。ERPs分析表明,双关图作为面孔刺激被识别时,T_3、Pz的P_2波潜伏期比双关图作为非面孔刺激被识别时分别延长6.09ms和7.39ms,波幅没有显著差异;双关图作为面孔刺激时T_3、T_4、Pz和Oz的P_3波的潜伏期比双关图作为非面孔刺激时延长约15ms;波幅没有显著差异。     

WITHIN‐SUBJECT REVERSIBILITY OF DISCRIMINATIVE FUNCTION IN THE COMPOSITE‐STIMULUS CONTROL OF BEHAVIOR

According to the composite-stimulus control model (Weiss, 1969, 1972b), an individual discriminative stimulus (S^D) is composed of that S^D''s on-state plus the off-states of all other relevant S^Ds. The present experiment investigated the reversibility of composite-stimulus control. Separate groups of rats were trained to lever-press for food whenever a tone or a light S^D was present. For one group, the nonreinforced S^Δ condition was tone-and-light absence ($\bar{T}$+$\bar{L}$). Tone-plus-light (T+L) was S^Δ in the other group. On a “stimulus compounding” test that recombined composite elements, maximum responding occurred to that composite consisting only of elements occasioning response increase. That was T+L for the group trained with $\bar{T}$+$\bar{L}$ as S^Δ and $\bar{T}$+$\bar{L}$ for the group trained with T+L as S^Δ. The S^Δ composite was next reversed over groups in Phase 2. In Phase 2 tests, maximum responding that was comparable in magnitude to that of Phase 1 was again controlled by the composite consisting only of elements most recently occasioning response increase—whether T+L or $\bar{T}$+$\bar{L}$. The inhibitory conditioning history of both composite-elements currently occasioning responding did not weaken the summative effect. These results confirm and extend Weiss''s composite-stimulus control model, and demonstrate that such control is fully reversible. We discuss how translating conditions of the stimulus-compounding paradigm to a composite continuum creates a functional and logical connection to intradimensional control measured through stimulus generalization, reducing the number of different behavioral phenomena requiring unique explanations.     

Differential responding without differential reinforcement: Intensity difference, continuum position, and reinforcement density effects

The response rates of five groups of rats were observed during exposure to different intensities of a four kilohertz tone within a two-component multiple schedule of nondifferential reinforcement. Response rates were found to be higher during the multiple schedule component which contained the higher intensity tone. Larger differences in response rates between the two multiple schedule components occurred with greater intensity separations (30 versus 20 decibels). At the 30 decibel separation a low absolute magnitude produced larger response rate differences than a high absolute magnitude, while at the 20 decibel separation a high absolute magnitude produced larger response rate differences. Increases in reinforcement density were accompanied by decreases in response rate differences between high and low intensity components only when over-all response rates also increased.     

Toward a technology of derived stimulus relations: an analysis of articles published in the journal of applied behavior analysis, 1992-2009

Every article on stimulus equivalence or derived stimulus relations published in the Journal of Applied Behavior Analysis was evaluated in terms of characteristics that are relevant to the development of applied technologies: the type of participants, settings, procedure (automated vs. tabletop), stimuli, and stimulus sensory modality; types of relations targeted and emergent skills demonstrated by participants; and presence versus absence of evaluation of generalization and maintenance. In most respects, published reports suggested the possibility of applied technologies but left the difficult work of technology development to future investigations, suggestions for which are provided.     

Stimulus control of habits: Evidence for both stimulus specificity and devaluation insensitivity in a dual-response task

Goal-directed and habitual actions are clearly defined by their associative relations. Whereas goal-directed control can be confirmed via tests of outcome devaluation and contingency-degradation sensitivity, a comparable criterion for positively detecting habits has not been established. To confirm habitual responding, a test of control by the stimulus–response association is required while also ruling out goal-directed control. Here we describe an approach to developing such a test in rats using two discriminative stimuli that set the occasion for two different responses that then earn the same outcome. Performance was insensitive to outcome devaluation and showed stimulus–response specificity, indicative of stimulus-controlled behavior. The reliance of stimulus–response associations was further supported by a lack of sensitivity during the single extinction test session used here. These results demonstrate that two concurrently trained responses can come under habitual control when they share a common outcome. By reducing the ability of one stimulus to signal its corresponding response–outcome association, we found evidence for goal-directed control that can be dissociated from habits. Overall, these experiments provide evidence that tests assessing specific stimulus–response associations can be used to investigate habits.     

Analysis of discriminative control by social behavioral stimuli

Visual discriminative control of the behavior of one rat by the behavior of another was studied in a two-compartment chamber. Each rat's compartment had a food cup and two response keys arranged vertically next to the clear partition that separated the two rats. Illumination of the leader's key lights signaled a “search” period when a response by the leader on the unsignaled and randomly selected correct key for that trial illuminated the follower's keys. Then, a response by the follower on the corresponding key was reinforced, or a response on the incorrect key terminated the trial without reinforcement. Accuracy of following the leader increased to 85% within 15 sessions. Blocking the view of the leader reduced accuracy but not to chance levels. Apparent control by visual behavioral stimuli was also affected by auditory stimuli and a correction procedure. When white noise eliminated auditory cues, social learning was not acquired as fast nor as completely. A reductionistic position holds that behavioral stimuli are the same as nonsocial stimuli; however, that does not mean that they do not require any separate treatment. Behavioral stimuli are usually more variable than nonsocial stimuli, and further study is required to disentangle behavioral and nonsocial contributions to the stimulus control of social interactions.