Determinants of tonic and phasic reactions in transswitching

Forty-eight college students were assigned randomly to four groups in a 2 × 2 factorial arrangement of phasic conditional stimuli (samevs. different) and tonic conditional stimuli (samevs. different) to receive 2 days of classical conditioning with a transswitching procedure. Tonic stimuli were a 5-minute projected white triangle or circle; phasic stimuli were a 5-second red or green square superimposed over the tonic stimuli. There were six tonic stimulus segments each day, separated by 20-second periods of no stimulus, three containing six trials of the phasic stimulus paired with shock and three containing six trials of the phasic stimulus alone, in the counterbalanced order. Tonic responding at the onset of the tonic stimuli or during brief periods following its onset were recorded, along with phasic responses to the phasic stimuli. Responses included magnitude of skin conductance responses, frequency of unelicited skin conductance responses, and tonic heart rate. Both skin conductance measures of responding to the tonic stimuli differentiated significantly between positive and negative tonic segments during Day 2, but only in the group with two different tonic stimuli and one phasic stimulus (“standard” transswitching). This supported the hypothesis that tonic stimulus differentiation would be absent when two different phasic stimuli were present. The heart rate data did not support this hypothesis, showing tonic differentiation in both groups with two tonic stimuli. Phasic differentiation controlled by the different phasic stimuli was observed on Day 1; on Day 2, phasic differentiation was present only in the group with two tonic and one phasic stimuli and the group with one tonic and two phasic stimuli. The results were interpreted to mean that temporal contiguity between the tonic stimuli and shock or no shock is not sufficient to establish tonic response differentiation in transswitching.     

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.     

Redundant information in an observing-response procedure

In three observing-response experiments relevant to the information hypothesis of conditioned reinforcement, the basic procedure was one in which an observing response produced one stimulus on trials that terminated in non-contingent reinforcement and another stimulus on trials that terminated in a brief timeout. In Experiment I, the observing response consisted of a single peck or a short fixed-ratio schedule (FR 3 or FR 6), depending on the type of trial. If the single peck produced the negative stimulus and the fixed ratio produced the positive stimulus, observing responses were maintained. If the single peck produced the positive stimulus and the fixed-ratio produced the negative stimulus, observing responses were not maintained on negative trials. In the second experiment, the response key was either white or dark at the beginning of a trial, indicating whether it was a positive or negative trial. Observing responses continued to be maintained on positive trials but not on negative trials. In Experiment III, only positive or negative trials were scheduled for several sessions. Observing responses extinguished regardless of whether positive or negative trials were scheduled. The results do not support the hypothesis that making the stimuli produced by observing responses redundant will reduce observing responses.     

Keeping Simon simple: Examining the relationship between sequential modulations and feature repetitions with two stimuli, two locations and two responses

The present study examined performance across three two-choice tasks that used the same two stimuli, the same two stimulus locations, and the same two responses to determine how task demands can alter the Simon Effect, its distribution across reaction time, and its sequential modulation. In two of the tasks, repetitions of stimulus features were not confounded with sequences of congruent and incongruent trials. This attribute allowed us to investigate the sequential modulation of the Simon Effect in a two-choice task while equalizing the occurrence of feature repetitions. All tasks showed a similar sequential modulation, suggesting that it is not driven by feature repetitions. Moreover, distributional analyses revealed that the advantage for congruent trials decreased as reaction time increased similarly following congruent and incongruent trials. Finally, a large increase in RT was observed when repeated responses were made to novel stimuli and when novel responses were made to repeated stimuli. This effect also showed a sequential modulation regardless of whether the stimulus repeated. The findings suggest that, even in two-choice tasks, response selection is mediated by complex, dynamic representations that encode abstract properties of the task rather than just simple features.     

Stimulus and response prediction in choice reaction time: Free vs. forced reactions

Verbal predictions were combined in a 1:many mapping in order to analyze the contribution of response preparation to both stimulus and response prediction effects in choice reaction time (RT). Using a three-stimulus, two-response task in which two of the stimuli were mapped 1:1 to separate responses (forced-choice) and the third stimulus was mapped to both responses (free-choice), response frequencies and latencies were compared in two experiments. The results indicated that (1) free-choice response selections were not influenced by forced-choice stimulus predictions; (2) free-choice RTs were reduced only when the free-choice stimulus was correctly predicted; (3) free-choice responses were generally consistent with the response predicted, but RT did not depend on response prediction; (4) on forced-choice trials, the RT difference between correct and incorrect predictions was similar for stimulus and response predictions; and (5) under no-prediction conditions, no difference was found between free and forced RTs. A stimulus anticipation component was the only apparent contribution to the stimulus prediction effect, while the response prediction data suggest some prior response selection with no associated decrease in latency     

Impact of contingency manipulations on accessory stimulus effects

Accessory tone stimuli facilitate response performance despite being irrelevant for the current task. In order to investigate which processes are affected by accessory stimuli, we presented accessory tones in a simple response time (RT) task while varying the contingencies between accessory stimulation and either responses(Experiment 1) or stimulus conditions (Experiment 2). Accessory tones speeded up responding to a larger degree when they were conjointly presented within go compared with no-go trials. In contrast, contingency variation with stimulus conditions did not alter the impact of accessory stimuli. Additionally, accessory tones increased response force. Thus, we conclude that in simple RT tasks accessory tones influence response-related stages such as response selection and response execution rather than perceptual processes.     

Paradoxical preference for more frequently occurring negative stimuli and for less frequently occurring positive stimuli as a function of amount of training in simultaneous discrimination learning

Development of a preference for more frequently occurring negative stimuli was found in a within-subject design. In this experiment, pigeons learned two simultaneous problems with an unequal number of training trials. At various stages in training, for example, the more-trained negative stimulus was paired with the less-trained negative stimulus for a single preference trial. These probe trials pointed to a swing in stimulus function in negative stimuli which also occurred at an earlier stage in positive (reward-correlated) stimuli. The paradoxical preference for less-trained positive over more-trained positive stimuli was found in this study, confirming the earlier reported phenomenon. The paradoxical preference for more-trained negative stimuli was discussed in terms of a frustration analysis. A symmetrical, albeit positive, emotional factor was discussed with regard to the paradoxical findings with positive probe trials.     

Positive and negative stimuli in relation to tennis players' reaction time

Research has indicated that negative and positive thoughts may affect sport performance. The purpose of this analogue study was to assess whether negative and positive stimuli influenced tennis performance similar to positive and negative thought. The reaction time (RT) of 40 competitive tennis players was measured during a timed response to a tennis ball rotating in a topspin, sidespin, or backspin direction on the computer screen. Immediately prior to the ball presentation, a phrase (accessory stimulus) was presented visually or aurally. The accessory stimulus provided either positive (e.g., 'nice shot') or negative information (e.g., 'bad shot') followed by the subject's name. Analysis showed a main effect only for the type of spin. The slowest RT occurred when responding to a tennis ball rotating in a backspin direction. A significant interaction was found for the sensory modality (audition vs vision) and polarity (positive vs negative) of the accessory stimulus. RT to negative stimuli was slowest when the accessory stimulus was presented aurally. The quickest RT to positive stimuli occurred when the accessory stimulus was presented aurally. These results indicated that negative and positive stimuli, when presented aurally, affected performance as positive and negative thoughts measured in other studies. Not measured was whether negative and positive stimuli actually produce the negative and positive thoughts, respectively, that have been reported to affect performance.     

Discrimination of polymorphous stimulus sets by pigeons

Pigeons were trained to perform a visual discrimination between stimulus sets in which the presence of any two of three positive features made a stimulus positive, while any two of three negative features made it negative (there were thus three different positive and three different negative stimuli). After training, the birds were exposed to test stimuli that contained either all three positive or all three negative features. In Experiment I three pigeons were successfully trained by a successive method, and subsequently responded to the test stimuli as though they were positive or negative respectively. In Experiment II four pigeons were trained by a simultaneous method. Three learned the discrimination and generalized appropriately to the test stimuli, but they showed no preference between positive test and positive training stimuli, nor any consistent difference in speed of response to them; and similar results were found for negative stimuli. It is argued from this that the pigeons learned to respond to the stimuli as patterns (configurations of features) rather than to the constituent features, but that they generalized to the test stimuli by using the common features. The experiments show that pigeons could in principle learn to discriminate natural polymorphous classes (such as “pigeon” or “person”) without using any single feature, but neither the present experiments nor earlier ones demonstrating discriminations of such natural classes establish that pigeons make use of polymorphous concepts in the same way as people.     

Discrimination of artificial polymorphous categories by rhesus monkeys (Macaca mulatta)

Monkeys (Macaca mulatta) were trained to discriminate between sets of artificial stimuli such as those used by Jitsumori (1993) for pigeons and humans. The stimuli were arrays of symbols differing along three two-valued (positive or negative) dimensions. The discrimination required was between polymorphous categories in which a positive stimulus was defined by possession of any 2 out of 3 positive features. Of the 5 monkeys, 3 learned the discrimination much faster than did pigeons, but transfer to novel stimuli was less impressive than had been shown in pigeons. The 3 monkeys showed high levels of transfer to the stimuli that contained either all 3 positive or all 3 negative features, but 2 of the 3 monkeys failed to show transfer to stimuli that had 1 of the 3 features replaced with a novel one. Analysis of the monkeys' performance raised doubts on the additive integration of features but supported learning of feature combinations as a basis for the discrimination of polymorphous categories by this species.     

Effects of short-term memory contents on short-and long-term memory searches

The Ss memorized a long-term set (LT set) of 20 words before participating in a recognition memory test. On each trial Ss were given a new short-term set (ST set) of from one to four words or one to four digits. The Ss gave a positive response to a test item that was a member of either the ST or the LT set and gave a negative response to a test item not in either set; both words and digits were used as test stimuli. The results indicated that reaction time (RT) to positive test items from the ST set was an increasing function 0f the size of the ST set; the same was also true for negative responses to test digits when the ST set was composed of digits. RT to other test stimuli, however, did not depend on ST set size. These results are consistent with the view that Ss access long-term memory (LTM) and short-term memory (STM) simultaneously rather than sequentially. The results also showed that Ss responded more quickly to test items from the LT set when the ST set contained digits than when it contained words. Negative test items that were words, however, were rejected more slowly when the ST set contained digits than when it contained words. These results suggest that the search of LTM was affected by the contents of STM.     

Effect of stimulus repetition on positive and negative identity priming

Most negative-priming experiments have used a limited number of stimuli that are repeated many times throughout the experiment. We report five experiments that examine in greater detail the role of stimulus repetition in negative priming. Subjects were presented with displays consisting of two or more words, and were required to name the word printed in red. On attended repetition (AR) trials, the target word was the same as the target word on the preceding trial. On ignored repetition (IR) trials, the target word was the same as the distractor word on the preceding trial. Experiments 1 and 2 used novel words, and obtained positive priming on AR trials, but no negative priming on IR trials. Experiments 3 and 4 used repeated words, and obtained negative priming on IR trials, but no positive priming on AR trials. In Experiment 5, both novel and repeated words were intermixed, and negative priming was observed for repeated, but not novel, IR conditions, whereas positive priming was observed for novel, but not repeated, AR conditions. Together, Experiments 1–5 demonstrate that positive and negative identity priming are modulated by stimulus repetition and are stimulus specific.     

The effect of comparative context on evaluative conditioning

Evaluative conditioning (EC) is a change in the evaluation of a stimulus after the stimulus co-occurred with affective stimuli. The present research examined whether EC of one stimulus depends also on the co-occurrence of another stimulus with positive or negative stimuli. We paired two target people with affective stimuli. We found that a person who appeared eight times with positive stimuli and eight times with negative stimuli was liked more when the other person appeared always (16 times) with negative stimuli than when the other person appeared always with positive stimuli. The manipulation did not change the US evaluation or the general standard on the value dimension of what a positive or negative stimulus is. We suggest that like other evaluative traits (e.g., evil, pretty) co-occurrence with affective stimuli is sensitive to temporary standards. The manipulation changed the standard of what co-occurrence with affective stimuli is considered positive versus negative.     

The motor side of emotions: investigating the relationship between hemispheres, motor reactions and emotional stimuli

The aim of the present study was to analyze if the left hemisphere preferentially controls flexion responses toward positive stimuli, while the right hemisphere is specialized toward extensor responses to negative pictures. To this end, right-handed subjects had to pull or push a joystick subsequent to seeing a positive or a negative stimulus in their left or right hemifield. Flexion responses were faster for positive stimuli, while negative stimuli were associated with faster extensions responses. Overall, performance was fastest when emotional stimuli were presented to the left visual hemifield. This right hemisphere superiority was especially clear for negative stimuli, while reaction times toward positive pictures showed no hemispheric difference. We did not find any interaction between hemifield and response type. Neither was there a triple interaction between valence, hemifield and response type. We suppose that response dichotomies in humans are not as tightly linked to a hemisphere- and valence-bound reaction type as previously assumed.     

前额叶神经振荡活动反映了稳固的刺激冲突和反应冲突

为考察典型Flanker任务中练习对刺激冲突和反应冲突的影响,本研究采用练习范式记录被试完成2:1字母Flanker任务时的行为和脑电数据。行为结果发现,练习对这两类冲突无显著影响。神经震荡能量结果发现,前额叶theta能量随练习而显著减弱,这暗示刺激-反应之间的联结因练习而提升;前额叶alpha能量差异不随练习而变化,这可能反映了Flanker任务中稳定的刺激冲突和反应冲突加工机制。因此,本研究揭示了典型Flanker任务中刺激冲突和反应冲突的稳定特征。     

Multiple stimulus discrimination learning. III. What is learned?

Rats were given a multiple stimulus discrimination, with either a constant positive stimulus combined with several negative stimuli or a constant negative stimulus combined with several positive stimuli. Choice data in transfer tests indicated that the discrimination had taken place on the basis of the constant stimulus alone and that the constant stimulus was equally effective in mediating transfer whether it had been positive or negative. While the multiple stimuli did not control choice behaviour, the latency data indicated that some analysis of them had taken place. Analyses of discrepancies in choice and latency data suggest that the two types of measure reflect different processes involved in discrimination learning.     

Bimanual response grouping in dual-task paradigms

In three experiments we measured response time (RT) and peak force (PF) to investigate the grouping of left- and right-hand key press responses in a dual-task paradigm involving two independent go/no-go tasks. Within each task, a go stimulus within one of two modalities (i.e., visual versus auditory) required a response by one hand. In Experiment 1 with simultaneous go stimuli in the two tasks, responses appeared to be grouped in approximately 75-80% of trials, compared with nearly 100% grouping in a single-task condition requiring bimanual responses to the onset of any stimulus in either modality. In Experiment 2 with stimulus onset asynchronies (SOAs) of 0-400 ms between the two go stimuli, response grouping clearly declined as SOA increased, although some grouping was still evident even at the longest SOA. The same pattern was observed in Experiment 3 with the same range of SOAs but unpredictable stimulus order, suggesting that grouping is not strongly dependent on prior knowledge of the likely response order. These results emphasize the pervasiveness of response grouping in bimanual dual-task RT paradigms and provide useful clues as to its nature.     

Control of impulsive emotional behaviour through implementation intentions

Past research has established that people can strategically enhance or override impulsive emotional behaviour with implementation intentions (Eder, Rothermund, & Proctor, 2010). However, it is unclear whether emotional action tendencies change by intentional processes or by habit formation processes due to repeated enactment of the intention (or both). The present study shows that forming implementation intentions is sufficient to modulate emotional action tendencies. Participants received instructions about how to respond to positive and negative stimuli on evaluation trials but no such trials were actually presented. Results showed that merely intending to approach and avoid affective stimuli influenced emotional action tendencies in a modified affective Simon task in which affective valence was irrelevant. An affective Simon effect (i.e., faster reactions when the valence of the stimulus corresponded with the valence of the movement) was observed when participants intended evaluations with affectively congruent responses (i.e., positive–approach, negative–avoid); in contrast, the effect was reversed in direction when participants planned evaluations with incongruent responses (i.e., positive–avoid, negative–approach). Thus, implementation intentions can regulate implicit emotional responses even in the absence of possible habit formation processes. Implications for dual-system accounts of emotion regulation are discussed.     

EQUIVALENCE CLASS FORMATION IN A TRACE STIMULUS PAIRING TWO‐RESPONSE FORMAT: EFFECTS OF RESPONSE LABELS AND PRIOR PROGRAMMED TRANSITIVITY INDUCTION

Three experiments identified factors that did and did not enhance the formation of two‐node four‐member equivalence classes when training and testing were conducted with trials presented in a trace stimulus pairing two‐response (SP2R) format. All trials contained two separately presented stimuli. Half of the trials, called within‐class trials, contained stimuli from the same class while the other half, called cross class trials, contained stimuli from different classes. On within class trials, making a YES response was correct and making a NO response was wrong. On cross class trials, making a NO response was correct and making a YES response was wrong. In Experiment 1, similar intermediate percentages of participants (about 50%) formed classes, regardless of whether the responses were labeled YES and NO or SAME and DIFF. Response labeling thus did not influence class formation. Regardless of response labels, failures of class formation were primarily due to failure of class‐indicative responding produced by within‐class transitivity probes. In Experiment 2, only 50% of participants formed classes without prior training, as in Experiment 1, but 100% of participants formed equivalence classes after the establishment of a generalized transitivity repertoire by use of a programmed transitivity induction protocol. Experiment 3 examined two components of the programmed transitivity induction protocol and found that the exclusion of AC trials had no effect on the percentage of participants who formed equivalence classes, while presenting the stimulus sets in randomized order interfered with equivalence class formation. A further analysis found that a number of stimulus control topographies differentiated between individuals who did and did not form equivalence classes. In general, then, these experiments demonstrate that equivalence classes can be formed reliably when training and testing are conducted in an SP2R format, supporting the view that equivalence class formation can account for the development of conceptual categories in natural settings.     

Ambiguous-cue learning in preschool children: A test of the dimensional characteristics of task stimuli

Sixteen preschool children were administered a two-choice discrimination problem consisting of three stimulus compounds: the consistently rewarded stimulus, the consistently nonrewarded stimulus, and the ambiguous stimulus which was nonrewarded when paired with the positive, but rewarded when paired with the negative. When both pair of stimuli, positive-ambiguous and negative-ambiguous, were presented together the subject was required either to choose or to avoid the ambiguous stimulus depending upon the stimulus with which it was paired. In Experiment 1, when each of three stimuli (positive, negative, ambiguous) varied along one nonspatial cue dimension (color), performance was better on negative-ambiguous trials than positive-ambiguous trials. In Experiment 2, when the positive and negative stimuli varied along three nonspatial cue dimensions (colors and form) and the ambiguous stimulus varied along one of these dimensions (color), superior positive-ambiguous over negative-ambiguous performance was obtained. These findings complement those reported for other subjects and confirm Berch's (D. B. Berch, Learning and Motivation, 1974, 5, 135–148) predictions regarding use of differential numbers of cue dimensions.