The opponent process theory and affective reactions

Solomon (1980) proposed an opponent process theory to account for motivational and affective dynamics. This theory asserts that the brain avoids extremes of emotional experience by countering the stimulation it receives with an opposite or opponent reaction. Opponent processes are thought to be responsible for the characteristic changes in affective experience that occur over time, and to account for the dynamics of affective response to such stimuli as skydiving and sauna bathing, which have heretofore been difficult to explain. However, the relevance of this theory for affective experiences in general (beyond physical stimuli and addictions) has yet to be demonstrated. The present paper examines opponent process theory predictions in two settings, involving affective responses to situation-scenarios and emotion-provoking slides. In each study, significant habituation to both positive and negative affective stimuli was found, as the opponent process theory would predict. Subjects also showed a reversal of affect when the stimuli were reversed from positive to negative or vice versa. However, contrary to opponent process theory predictions, there was no evidence that withdrawal responses were greater after habituation to the affective stimulus. The only instance of a significant difference in withdrawal responses was actually in a direction opposite to that which the opponent process theory predicts. All other predicted differences were not significant. The opponent process theory, therefore, was not supported in these data and appears to need revision or qualification as to its domains of application.     

Responding to emotional scenes: effects of response outcome and picture repetition on reaction times and the late positive potential

Processing the motivational relevance of a visual scene and reacting accordingly is crucial for survival. Previous work suggests the emotional content of naturalistic scenes affects response speed, such that unpleasant content slows responses whereas pleasant content accelerates responses. It is unclear whether these effects reflect motor-cognitive processes, such as attentional orienting, or vary with the function/outcome of the motor response itself. Four experiments manipulated participants’ ability to terminate the picture (offset control) and, thereby, the response’s function and motivational value. Attentive orienting was manipulated via picture repetition, which diminishes orienting. A total of N?=?81 participants completed versions of a go/no-go task, discriminating between distorted versus intact pictures drawn from six content categories varying in positive, negative, or neutral valence. While all participants responded faster with repetition, only participants without offset control exhibited slower responses to unpleasant and accelerated responses to pleasant content. Emotional engagement, measured by the late positive potential, was not modulated by attentional orienting (repetition), suggesting that the interaction between repetition and offset control is not due to altered emotional engagement. Together, results suggest that response time changes as a function of emotional content and sensitivity to attention orienting depends on the motivational function of the motor response.     

Reinforcement of spaced responding in a simultaneous discrimination

Pigeons were exposed to three stimuli simultaneously with responses reinforced according to differential-reinforcement-of-low-rate schedules. Responses to one stimulus (the positive stimulus) that were spaced appropriately resulted in food presentation. The variables manipulated were the time parameter of the schedule (5, 10, 20, 30 sec) and the consequences of responding to the other two stimuli (the negative stimuli). The percentage of the total responses that occurred to each stimulus was independent of the schedule value but was dependent on the consequences of responding to the negative stimuli. If responses to both reset the schedule timer, responding was confined largely to the positive stimulus. If responses to neither had scheduled effects, the birds were more likely to respond to those stimuli. Responding to one negative stimulus could be selectively attenuated by having responses to that stimulus alone reset the timer. With the schedule time value held constant, the absolute rate of responding to the positive stimulus was either stable or decreased with maintained exposure; it did not change as a function of increases or decreases in responding to the negative stimuli. Rather than interacting and affecting each other, responses to the three stimuli were controlled independently by their relation to reinforcement. There was no evidence that responses to the negative stimuli mediated the spacing of responses to the positive stimulus.     

Depth of facial expression processing depends on stimulus visibility: Behavioral and electrophysiological evidence of priming effects

Participants performed a priming task during which emotional faces served as prime stimuli and emotional words served as targets. Prime-target pairs were congruent or incongruent, and two levels of prime visibility were obtained by varying the duration of the masked primes. To probe a neural signature of the impact of the masked primes, lateralized readiness potentials (LRPs) were recorded over motor cortex. In the high-visibility condition, responses to word targets were faster when the prime-target pairs were congruent than when they were incongruent, providing evidence of priming effects. In line with the behavioral results, the electrophysiological data showed that high-visibility face primes resulted in LRP differences between congruent and incongruent trials, suggesting that prime stimuli initiated motor preparation. Contrary to the above pattern, no evidence for reaction time or LRP differences was observed in the low-visibility condition, revealing that the depth of facial expression processing is dependent on stimulus visibility.     

Simon congruency effects based on stimulus and response numerosity

Three choice reaction time experiments documented a Simon-type congruence effect involving the numbers of stimuli and responses. In Experiment 1 the stimulus consisted of one or two high- or low-pitch tones, and participants were required to respond with one or two taps of a response key depending on stimulus pitch. Responses were faster when the number of tones matched the required number of response taps than when these numbers mismatched. Experiment 2 showed that a weaker version of this effect can also be obtained using visual stimuli, and Experiment 3 showed that the analogous effect can even be obtained, albeit very weakly, with bimodal stimuli. There was also evidence that the number of stimuli affected the rate of emitting the two-tap response. These results indicate that stimulus numerosity is processed automatically to the level at which it can affect the selection and possibly the execution of a varying number of responses.     

Simon congruency effects based on stimulus and response numerosity

Three choice reaction time experiments documented a Simon-type congruence effect involving the numbers of stimuli and responses. In Experiment 1 the stimulus consisted of one or two high- or low-pitch tones, and participants were required to respond with one or two taps of a response key depending on stimulus pitch. Responses were faster when the number of tones matched the required number of response taps than when these numbers mismatched. Experiment 2 showed that a weaker version of this effect can also be obtained using visual stimuli, and Experiment 3 showed that the analogous effect can even be obtained, albeit very weakly, with bimodal stimuli. There was also evidence that the number of stimuli affected the rate of emitting the two-tap response. These results indicate that stimulus numerosity is processed automatically to the level at which it can affect the selection and possibly the execution of a varying number of responses.     

Psychological analyses of haptic and haptic-visual judgements of extent

Magnitude estimates of haptic extent resulted in positively accelerated psychophysical power function with an exponent of 1.18. However, in two further experiments right-handed male subjects made rating-scale judgements of the combined width of two stimulus blocks. Six widths were used and five replications of the 36 factorial combinations were presented to each subject. In Experiment II both stimuli were out of view and one was held between the thumb and index finger of each hand. In Experiment III one stimulus was held out of view between thumb and finger of the right hand and the second was shown to the subject. Mean ratings in both experiments were fit by a model which assumes that responses are a weighted average of the scale values of the two stimuli (Anderson, 1974a).     

Physical and cognitive dimensions in stimulus comparison

Two experiments were carried out using a same-different task with sets of four stimuli varying orthogonally in three dimensions. Sameness was defined by each of the three dimensions in turn, as well as by physical identity. Two types of dimensions, physical and cognitive, were studied. In Experiment 1, the numerals 6, 10, VI, and X, which vary in Length, System, and Name, were used. With simultaneous presentation, order of difficulty was from the physical dimension of Length to the cognitive dimension of Name. While overall difficulty was related to dimensional discriminability, internal evidence suggested that Name was not a dimension in the same sense as Length is, and that some stimulus pairs were simply easier to process than others, regardless of the response required (e.g., short stimulus pairs and Arabic numerals). With sequential presentation, Name was processed as fast as System, due largely to the fact that much faster responding occurred when an Arabic numeral was the second stimulus. Thus, with sequential presentation, Name provides a processing mechanism not provided by physical dimensions. In Experiment 2, the numerals 3, 4, 6, and 7, which vary in Magnitude, Oddness, and Curvilinearity, were used. The cognitive dimension of Magnitude was pro cessed most rapidly, and numerical distance between pairs of numbers dominated the results for “same” responses, regardless of the sameness rule used. Again, evidence was found for fast processing of some stimulus pairs (e.g., 3 4), regardless of the response required. Overall, these experiments are interpreted as indicating that cognitive factors such as stimulus familiarity may override aspects of physical discriminability with many dimensions and stimuli, that, even though a cognitive dimension can be used to generate a logically proper set of stimuli, it does not necessarily act as other, more physical dimensions do, and that clarification of the functional role of a dimension is more important than attempts to locate stages.     

Behavioural arousal and its habituation in the squirrel fish, Holocentrus rufus: the role of the telecephalon

Squirrel fish were captured, maintained for 2 days and then tested for their responses to stimuli in laboratory aquaria. A tap on the side of the aquarium or a shadow moving overhead elicited an arousal response involving a reduction in opercular movements, movement of the pectoral fins, and erection of the spiny dorsal fin. This latter response, when regularly provoked by a moving shadow at 15-s intervals, decreased in duration and habituated. When fish were restricted in a wire mesh trough and the stimulus was the onset of illumination to one eye at 15-s intervals, responses were quantitatively similar although shorter in duration. A series of stimuli delivered to one eye until habituation followed by a series to the other eye reduced the duration of initial responses and the number of trials for habituation of responses to stimuli delivered to the second eye. Responses were equivalent regardless of which eye (left or right) was first presented with stimuli. Section of the telencephalic anterior commissure considerably restricted the transfer of information about experience of stimuli presented to the first eye. Commissural section, combined with unilateral lesions in the posterior-medial telencephalon, severely impaired habituation of responses to the contralateral eye. Lateral lesions had no effect. The results are discussed in relation to the visual projection in Holocentrus and telecephalic involvement in arousal and its habituation in teleosts as a whole.     

Discriminated timeout avoidance in pigeons: the roles of added stimuli

Two experiments examined pigeons' postponement of a signaled extinction period, or timeout (TO), from an ongoing schedule of response-dependent food delivery. A concurrent-operant procedure was used in which responses on one (food) key produced food according to a variable-interval schedule and responses on a second (postponement) key delayed the next scheduled TO according to a response-TO (R-TO) interval. A series of response-independent stimulus changes on the food key temporally partitioned the R-TO into three equal segments (S1, S2, and S3). Postponement responses, in addition to postponing TO, also reinstated S1, the stimulus correlated with the greatest temporal distance from TO. In Experiment 1, the R-TO interval was manipulated systematically across blocks of sessions (conditions) at a given ratio of R-TO:TO duration. This R-TO:TO ratio was manipulated across blocks of conditions (phases). Postponement response rates varied inversely with R-TO interval in each phase. Changes in the R-TO:TO ratio did not produce consistent differences except at the 1:10 ratio for some pigeons, where it disrupted postponement responding in some conditions. Most of the postponement responses occurred in the presence of S2 and S3, the stimuli most proximal to TO, whereas most of the food-key responses occurred in S1. In Experiment 2, the R-TO contingencies were systematically manipulated in the presence of the time-correlated stimuli. In one set of conditions, the R-TO contingencies were made either ineffective or less effective in the presence of one or more stimuli. Postponement responses typically shifted to stimuli in the presence of which responses were relatively more effective. Postponement responses decreased markedly when the added stimuli were removed, and then recovered when the stimuli were reinstated. Results from both experiments indicate that the added stimuli in a discriminated TO-avoidance procedure serve predominately discriminative functions, delineating periods during which behavior is maximally effective. The results parallel those obtained in shock-avoidance procedures, providing further evidence that TO functions as an aversive stimulus.     

Stimulus control of differential-reinforcement-of-low-rate responding

Five pigeons were given single-stimulus training on an 8-sec differential-reinforcement-of-low-rate schedule followed by steady-state generalization training using 12 wavelength stimuli. Three birds had a high percentage of reinforced responses on the training schedule and flat generalization gradients of total responses. The birds with fewer reinforced responses had much steeper generalization gradients. Generalization gradients plotted as a function of both stimulus wavelength and interresponse time showed that for most birds, stimulus control was restricted to responses with long interresponse times. Responses with very short interresponse times were not under stimulus control and there was some evidence of inhibitory control of short interresponse times. Interresponse-times-per-opportunity functions, plotted as a function of stimulus wavelength, showed that stimulus wavelength controlled the temporal distribution of responses, rather than the overall rate of response. The data indicate that the differential-reinforcement-of-low-rate schedule generates several response categories that are controlled in different ways by wavelength and time-correlated stimuli, and that averaging responses regardless of interresponse-time length obscures this control.     

Attention bias towards personally relevant stimuli: the individual emotional Stroop task

The emotional Stroop task is a widely used method for investigating attentional bias towards stimuli due to mood or affect. In general, standardized stimuli are used, which might not be appropriate when investigating individual contextual frameworks. It was investigated whether words chosen to be related to individuals' personal life events would produce more pronounced Stroop interference (as an indicator of attentional bias) than stimuli without any personal relevance. Twenty-six nonclinical subjects, 20 female and 6 male, participated in the study. Mean age was 36.1 yr. (SD = 18.1). All were recruited by means of local advertising. Stimulus material consisted of four word types: personal words related to negative life events with and without current personal relevance, and negative and neutral words without any personal relevance. Words were presented in three blocks. Analysis of variance showed main effects for word type and blocks, with slower reactions in the personally relevant conditions than in the negative, or neutral conditions, and in response to the first blocks as opposed to the last. These findings indicate that regardless of the word valence, personally relevant stimuli evoke more pronounced Stroop interference than do stimuli without personal relevance.     

Preference as a function of the correlation between stimuli and reinforcement outcomes

Pigeons' preferences for stimuli that were to varying degrees correlated with outcomes were studied in two experiments using a concurrent-chain procedure. The pigeons chose between two terminal links, each ending with food reinforcement and with blackout on half of the trials. In the first experiment, one terminal link (nonpredictive or unreliable link) provided stimuli completely uncorrelated with the outcomes while the other terminal link (predictive or reliable link) provided stimuli that were, to varying degrees, correlated with these outcomes. All pigeons showed increasing preferences for the predictive link as the reliability of the stimuli in that link increased. In the second experiment, stimuli in both terminal links were differentially correlated with the outcomes. The pigeons again preferred the more reliably correlated terminal link. The relation between these results and the delay-reduction hypothesis and conditioned reinforcement account is noted. The behavioral value of predictive stimuli may lie in their permitting the organism to more effectively apportion its time between interim activities and terminal responses.     

Repetition effects in choice reaction time to multidimensional stimuli

Ss classified as quickly as possible stimuli back-projected one at a time on a small screen by pressing one of two levers in response to each stimulus, according to the levels of a single specified binary stimulus dimension. Stimuli were rectangles varying in height alone, in width alone, or in both dimensions, in either a correlated or an orthogonal fashion. Stimuli followed responses by a fixed interval of 82, 580, or 1,080 msec. Response time was longer when both dimensions varied orthogonally than when only one dimension varied, indicating that Ss were unable to avoid perceiving the rectangle figures as wholes. Repeated stimuli were responded to more quickly than stimuli which were different from the immediately preceding stimulus in all conditions. With orthogonally combined dimensions, response time to stimulus repetitions was lowest, increased when the stimulus changed while the response was repeated, and increased still further when both the stimulus and the response changed. Increasing the time interval between stimuli decreased response time for nonrepetitions, while response time for repetitions was relatively unaffected. The results were discussed in terms of two models of serial choice reaction time.     

Attachment insecurity and strategies for regulation: when emotion triggers attention

Attachment-related strategies are thought to be critical for regulation and processing of emotional information. This study examined biases in selective attention to emotional stimuli as a function of insecure attachment. Participants searched for a single target image preceded by to-be-ignored distracters depicting emotional images varying in valence and arousal. Results revealed that, in general, negative distracters affected accuracy levels, and that the anxious attached participants showed a clear interference of the emotional distracters. In contrast, the avoidant group evinced a higher control on such interference. In addition, arousal ratings to distracter images indicated superior emotional activation only for anxious attached participants. Consistent with the evolutionary-based attachment theory threat-related stimuli prompted priority attentional responses. Present findings are in line with evidence showing the deployment of distinct strategies in insecurely attached individuals for the regulation of attention to emotional information.     

The threshold for successiveness

In Experiment 1, three stimuli were presented on each trial; the second and third were simultaneous. Ss said which of the three they saw first and then made a different second guess. Second guesses were correct more often than chance when first guesses were wrong, contradicting the predictions of a psychological moment theory. Psychometric functions are inconsistent with a theory which holds that Ss can order their perceptions and that errors result from lack of correspondence between this order and that of the stimuli. In Experiment 2, two pairs of stimuli, each simultaneous or successive, were presented on each trial, the interval between their onsets varying, and Ss guessed whether each was successive. A moment-like cyclic process affecting the perception of successive stimuli should raise the correlation between responses when both pairs were successive and beginning at the same time; this was not found.     

Temporal dynamics of unimodal and multimodal feature binding

In two experiments, we studied the temporal dynamics of feature integration with auditory (Experiment 1) and audiovisual (Experiment 2) stimuli and manual responses. Consistent with previous observations, performance was better when the second of two consecutive stimuli shared all or none of the features of the first, rather than when only one of the features overlapped. Comparable partial-overlap costs were obtained for combinations of stimulus features and responses. These effects decreased systematically with increasing time between the two stimulus-and-response events, and the decreased rate was comparable for unimodal and multimodal bindings. General effect size reflected the degree of task relevance of the dimension or modality of the respective feature, but the effects of relevance and of temporal delay did not interact. This suggests that the processing of stimuli on task-relevant sensory modalities and feature dimensions is facilitated by task-specific attentional sets, whereas the temporal dynamics might reflect that bindings “decay” or become more difficult to access over time.     

The role of generation in recognition

In contrast to the widely accepted opinion, a negatively accelerated RT function was obtained with varied mapping of stimuli to responses in Sternberg's (1966) recognition task when the task was designed to reduce proactive inhibition. These results are similar to the results obtained in the distractor task. Those aspects of the distractor task that proactively inhibit recall of the trigram are also necessary to produce a linear RT function in the recognition task. Hence, the varied-set procedure only results in a linear RT function when the memory sets on successive trials contain similar items, but not when successive trials contain different kinds of items, e.g., digits versus letters. Also, once subjects have been trained on the fixed-set procedure to produce a negatively accelerated RT function, the training transfers completely and immediately to entirely new sets of targets and distractors. The results of both tasks, as well as other retrieval tasks, can be explained by a model containing a single comparison process and an optional serial generation process which is invoked to increase the discriminability of the memory set from distractors.