Stimulus novelty and intraseries primacy in GSR adaptation

GSR records were obtained for four groups of 20 Ss. Group I was presented with a series of four different lights (amber, blue, green, and white) appearing 20 times each, in apparent random order. The procedure was similar for the other three groups except that in group 2, a novel stimulus (a red light) appeared instead of the sixth amber light; in group 3, it appeared instead of the 16th amber light; and, in group 4, it appeared instead of the 16th amber light. Typical GSR adaptation phenomena were observed in all groups. The introduction of the novel stimulus appeared to have no effect on the course of GSR adaptation.     

Stimulus novelty and intraseries primacy in GSR adaptation

GSR records were obtained for four groups of 20 Ss. Group I was presented with a series of four different lights (amber, blue, green, and white) appearing 20 times each, in apparent random order. The procedure was similar for the other three groups except that in group 2, a novel stimulus (a red light) appeared instead of the sixth amber light; in group 3, it appeared instead of the 11th amber light; and, in group 4, it appeared instead of the 16th amber light. Typical GSR adaptation phenomena were observed in all groups. The introduction of the novel stimulus appeared to have no effect on the course of GSR adaptation.     

Effects of real vs pretend shock on semantic differential judgments and the GSR in some classical conditioning paradigms

In two experiments subjects were shown different color 1-sec lights, one just before the end of a 4-sec UCS and the other coming 10 sec after UCS termination and 25 sec before the next UCS. For some groups the UCS was strong electric shock; for others it was a tone which subjects were instructed to imagine was a strong shock. The primary data were changes in semantic differential ratings of the lights before and after 12 “conditioning” trials. There were no differences among the groups. In a third experiment a 6-sec delay CS was used for GSR conditioning, some subjects receiving actual shock and others pretend shock. Only the former showed conditioning. The results are discussed in terms of a model of experimental demand.     

Reaction time task as unconditional stimulus

The present study was conducted to demonstrate classic conditioning in electrodermal (ED) and heart rate (HR) responses by using a nonaversive reaction time (RT) task as unconditional stimulus (US). Three groups of 12 subjects each were studied to test the efficacy of this US procedure by varying the essential components of the RT task-US between groups. Eight seconds differential delay conditioning was applied in each group. Simple geometric features (square, cross) displayed on a TV screen were used as CS+ and CS−. RT task consisted of a nonaversive tone (72 dBA, 1000 or 1200 Hz) and a motor response (pressing a button with the left index finger). Subjects were asked to respond as soon as the tone stimulus was presented. The three groups received different stimulus sequences during the 16-trial acquisition phase only. In one group (Group C1), CS+ was followed by a tone to which subjects were to respond, whereas CS− was not followed by a tone. Similarly, in a second group (Group H), CS+ was followed by a tone, whereas CS− was not; however, subjects of Group H (habituation group) were not required to respond to the tone. In a third group, (Group C2) CS+ was followed by a tone to which subjects were to respond, while CS− was followed by a different tone requiring no response. According to analysis of Group C1 data, differential conditioning was obtained in each response measure. Group H displayed habituation in each response measure obtained. In Group C2, differential conditioning was obtained in the second latency window of ED responses only. In all trials, first-interval anticipatory ED responses and HR responses did occur during acquisition, but were not differentiated with respect to the CS conditions. Although the results of Group C2 need further exploration, differential conditioning of HR and in all latency windows of ED responses was demonstrated by the use of a nonaversive RT task as US.     

Cognitive conditioning: Imagined stimulus contiguity and the third interval conditional GSR

The effect of repeatedly imagining paired or unpaired CSs and USs on the frequency of post-CS responses during real extinction was studied. Four groups of 10 Ss first received a model tone and shock. For two of the groups the stimuli were paired (delayed conditioning paradigm). For the others the stimuli were arranged in a long trace paradigm. The Ss then received a series of commands requiring them to imagine receiving paired CSs and USs, or to imagine the events singly. Then 10 real tone extinction trials were given. The groups which received delayed conditioning model stimuli were more responsive than trace groups, and groups which had imagined paired stimuli were more responsive than their unpaired controls. Cognitively oriented explanations of these findings were discussed.     

Stimulus information and stimulus interference in bisensory short-term memory

An attempt was made to determine if Ss’ strategy of retaining stimulus material changed under conditions of bisensory simultaneous stimulation when one of the two inputs was relevant information as opposed to interference. Thus in Group 1 Ss were stimulated bisensorily, attended to both inputs (information), but recalled only one input. Ss in Group 2 were stimulated bisensorily, attended to only one input, and recalled only that input (interference). It was found that S’s efficiency of recall was decreased in the information condition (Group 1) but strategy was not altered. In both groups, Ss performed similarly; performance was in turn similar to that observed in the typical bisensory situation, i.e., where both channels are recalled.     

Paired comparison scaling of reaction potential from simultaneous measurements of GSR and looking time

Thurstone’s method of scaling from paired comparison data was employed to obtain estimates of reaction potential on eight successive presentations of randomly generated polygons. One set of scale values was based upon the magnitude of the GSR made by each of 40 Ss to the onset of each stimulus. Another set of scale values was based upon the Ss looking times, when the S was instructed to press a switch to terminate the stimulus after he finished looking at it. Following termination of each stimulus, a 20-sec period of no stimulation intervened prior to the next stimulus. The GSR reduced in size from trial to trial, describing a typical habituation curve, while looking time increased from trial to trial. Across trials the two sets of scale values were significantly negatively correlated (r=?0.91). The failure to find habituation of looking time was explained on the assumption that the 20-sec period between stimuli was noxious to the Ss, which resulted in longer and longer looking times across trials. These results were interpreted as indicating that habituation of the GSR is not merely a matter of reduced attention in the cognitive sense. In addition, it was pointed out that the use of orienting reflex concepts in dealing with attentional and other cognitive phenomena may be unjustified.     

A stimulus-compounding assay of conditioned inhibition and excitation

Rats were trained in an operant discrimination involving two panel lights, A and B. Group CI (Conditioned Inhibition) was trained to lever press in the presence of A (S+), and not in the presence of the compound AB (S?). The opposite contingencies held in Group CE (Conditioned Excitation). Response rates were higher in Group CE than in Group CI, especially to the positive stimulus. However, the groups acquired the discrimination at comparable rates. In a separate phase of the experiment, a tone (C) was separately trained in the absence of the lights to control responding. All seven possible combinations of A, B, and C were then presented randomly during extinction. The inhibitory effect of B on C in Group CI was comparable in magnitude to the excitatory effect of B on C in Group CE. B's effect on C was not altered by the presence or absence of A, regardless of whether A was inhibitory or excitatory. The symmetry between CI and CE revealed by the stimulus-compounding test may be partly artifactual.     

Confidence ill stimulus predictions and choice reaction time

In two choice reaction time (RT) experiments, a stimulus prediction and a confidence judgment in the prediction preceded each occurrence of one of two stimulus alternatives. Ss identified each stimulus presentation by pressing a left-hand or right-hand telegraph key. In Experiment I the source of the stimulus predictions and confidence estimates was varied between groups of 20 Ss. For each condition, RT to correctly predicted stimuli was an inverse function of prediction confidence. Following incorrectly predicted stimuli, RT was not reliably influenced by confidence when S gave both predictions and confidence judgments; but RT to incorrectly predicted stimuli was an increasing function of confidence when E verbalized the predictions and confidence estimates or when S predicted and E indicated confidence. In Experiment II Ss made predictions and the validity of Es confidence estimate was manipulated between Ss. When Es confidence was perfectly related to the probability of a correct prediction, choice RT to nonpredicted stimuli was inversely related to confidence. However, choice RT to nonpredicted stimuli was not affected by prediction confidence when Es judgments were random.     

Aversive and compensatory classical conditioning with diazepam as conditional stimulus

The purpose of the first experiment was to investigate whether diazepam could acquire anxiogenic properties by signalling an aversive event. Rats were trained in an operant chamber in the pentylenetetrazol (PTZ) model of anxiety. Thereafter the animals were divided into groups that received classical diazepam conditioning (Group 1), and conditioning of diazepam + tone (Group 2). In the test phase diazepam was injected prior to placement in the operant chamber. Group 2 selected the PTZ-appropriate lever more often than the other groups, indicating that the tone induced anxiety, and diazepam did not. Tones and shock may therefore be more easily associated than diazepam and shock. The second experiment investigated this. Rats were trained the same way as in the first experiment. Thereafter the experimental group received injections of a small dose of diazepam prior to a second injection of a large dose of diazepam. The hypothesis was that a compensatory anxiogenic conditional response to diazepam's anxiolytic effect should be elicited by the small dose. There were no differences between the groups in lever selection, indicating that a compensatory anxiogenic response was not elicited.     

The effect of UCS intensity in classical and avoidance GSR conditioning

This study compared GSR avoidance and yoked-control conditioning procedures. Classical conditioning at two UCS intensities was followed by extinction and, two months later, by an avoidance session. Matching of Ss was based on GSR responsiveness and classical conditioning in the first session. The strong UCS led to more rapid reduction in CR latency (due to an increase in number of Ss responding) in the first session, and there was a tendency for maximum CR magnitude to occur in fewer trials with the strong UCS. No UCS-intensity difference in level of responding to the CS or UCS was found in the first session. A greater amount of spontaneous recovery in the second session was found in the strong UCS group. The avoidance and yoked control groups did not differ in CR magnitudes, latencies, or frequencies, nor in UCR magnitudes in the second session. They did differ significantly in the rate of decline in intertriai responses, the decline being more rapid in the avoidance condition.     

Individual response patterns in binary choice tasks with nondiscriminable stimuli

The present experiment sought to determine whether individual Ss tend to employ repeatedly the same response patterns in binary choice tasks containing nondiscriminable stimuli and, if so, whether the response sequences when used to constructstimulus sequences improve the performance of other choice tasks. Information and frequency analyses of the response sequences of 48 Ss showed moderate consistency of patterning within a light and within a tone task. Performance of a card task following the light and tone tasks was closely related to the task (light or tone) from which the stimulus sequence was obtained. The frequency analysis showed that repetition patterns were preferred by most Ss but at the expense of alternation responses. The presentation of reinforcement in the card task did not improve performance over that observed in the light and tone tasks.     

提取-消退范式中复合刺激对恐惧消退的影响

情绪障碍治疗的关键在于消退条件性恐惧记忆,研究证明基于记忆再巩固的提取-消退范式能有效消除或改写原有的恐惧记忆。本研究将提取-消退范式应用到更复杂的恐惧记忆中,采用多感官复合刺激(声音+图片)作为条件刺激,以皮电反应作为恐惧反应指标,考察采用单个线索(声音或图片)、复合线索(声音+图片)进行提取-消退对条件性恐惧记忆的消退效果有何差异。结果表明:声音线索提取-消退组出现了自发恢复和重建效应,图片提取-消退组只出现了重建效应,复合刺激提取-消退组未出现自发恢复和重建效应。说明由复合刺激线索引发的条件性恐惧,采用复合刺激中的单个较强线索或原有完整线索进行提取-消退,对恐惧记忆的消退效果最好。     

Individual response patterns in binary choice tasks with nondiscriminable stimuli

The present experiment sought to determine whether individual Ss tend to employ repeatedly the same response patterns in binary choice tasks containing nondiscriminable stimuli and, if so, whether the response sequences when used to construct stimulus sequences improve the performance of other choice tasks. Information and frequency analyses of the response sequences of 48 Ss showed moderate consistency of patterning within a light and within a tone task. Performance of a card task following the light and tone tasks was closely related to the task (light or tone) from which the stimulus sequence was obtained. The frequency analysis showed that repetition patterns were preferred by most Ss but at the expense of alternation responses. The presentation of reinforcement in the card task did not improve performance over that observed in the light and tone tasks.     

Short-term memory for a pure-tone stimulus among mentally retarded and nonretarded persons

Two studies were conducted to determine whether short-term memory performance differences between mentally retarded and nonretarded persons can be attrubuted to the operation of structural features, as contrasted with strategic control processes. The task—discrimination of intensity differences between two pure tones—was selected as one which would minimize specific strategy utilization. In the first experiment normal children, normal adults, and retarded adults were presented with a standard tone and then a comparison tone after an interval of 1, 5 or 10s. Difference limens and constant errors were computed over a substantial number of trials. Measures of intra-individual variability were also obtained. Clear age and IQ-related threshold differences were obtained. Difference thresholds increased over intervals for all groups. However, the critical interaction that would support a theory of differential decay of the memory trace was not obtained. A second experiment, procedurally similar to the first, was conducted using signal detection methodology. The major findings were: (a) groups differed in sensitivity (d′); (b) d′ decreased with increasing separation of standard and comparison tones; (c) d′ increased as the intensity differences between standard and comparison tones increased; and (d) retarded subjects did not alter response bias to changing task requirements Again, however, the interaction of groups and retention interval was not significant. Intelligence and age-related differences in the task occur early in the information processing sequence and appear to be of a perceptual nature.     

Tonic and phasic stimulus control of blood pressure responses using opposing unconditional stimuli

The transswitching paradigm was used in the present study to investigate the effects of tonic (long duration) environmental stimuli paired with opposing unconditional stimuli on human blood pressure. Sixty volunteers participated for two sessions, one week apart. Subjects were presented with a pseudorandom sequence of four trials of red lights (five minutes each) and four trials of blue lights (five minutes each) within each session. All subjects received the cold pressor test during the red lights. During the blue lights, half the subjects received warm water and the other half received a neutral temperature water. Subjects received the presentations of the water in one of three methods: as determined by the experimenter, preceded by a warning signal, or self-administered. The results indicated that conditional and unconditional responses during the red lights were progressive increases in blood pressure. During the blue lights associated with warm water, conditional and unconditional responses were often progressive decreases in blood pressure. The method of administration of the water affected the magnitude of the unconditional responses. Evidence for phasic stimulus control was not as unequivocal as tonic stimulus control. The present results indicated that it is possible to modify blood pressure in two directions (increases and decreases) when two high contrast, opposing unconditional stimuli are presented.     

Avoidance responding as a function of stimulus duration and relation to free shock

Response-independent pairings of a tone and a brief shock were superimposed on uncued avoidance responding in four groups of rhesus monkeys. For one group, tone presentations were immediately followed by an unavoidable electric shock; for the remaining groups, gaps of 5, 20, and 80 sec intervened between tone termination and shock delivery. These temporal values subsume paradigms usually treated as discrete procedures; the conditioned emotional response procedure (0-sec gap between tone and shock), trace procedure (5-sec gap) and safety-signal training (80-sec gap). Within each group, tone durations of 10, 20, 40, and 80 sec were examined. A response pattern marked by maximum response rate in the initial 5 sec of the tone followed by deceleration before shock was observed when shock immediately followed the tone, but not when gaps were interposed between the tone and shock. Response rates in the first 5 sec of the tone were a function of both tone duration and duration of the gap. When the gap was 0 to 5 sec, initial response rates were highest in longer duration tones; this relationship between tone duration and initial tone response rate was not observed for longer gaps.     

The effects of stimulus structure and familiarity on same-different comparison

It was hypothesized that performance in the same-different comparison task is based on two modes of processing: (1) structural processes that organize the detailed parts of a stimulus into a well-formed whole, and (2)analytic processes that decompose the stimulus into features. This hypothesis was supported, but with the unexpected finding of individual differences in the mode of processing underlying “same” responses. Those Ss in the “same” condition whose reaction times were faster for symmetrical than for asymmetrical patterns supported the hypothesis for structural processes. The remaining Ss in the “same” condition, as well as all the Ss in the “different” condition, were unaffected by symmetry. These Ss supported the hypothesis for analytic processes. Although familiarity effects were obtained for both structural and analytic Ss, the rotation of the familiar patterns into an unfamiliar orientation virtually eliminated familiarity effects for the structural Ss, but left them intact for analytic Ss.     

Sleep and overextinction of the GSR component of the orienting response

Overextinction of the GSR component of the orienting response was examined in a sample of 68 socially disturbed adolescents. Continued stimulus repetition beyond the point of habituation resulted in GSR return after 50–60 stimulus presentations. However, division of Ss into sleep and non-sleep groups using behavioral and self-report criteria, failed to support Sokolov’s (1963) notion that overextinction is accompanied by drowsiness. A possible explanation of these results is discussed.     

Elicitation and Inhibition of Competitive Fighting in Food Deprived Mice

Habituation as an index of the intrasensory and intersensory integration of form was investigated in nine-year-old children. In Habituation Period One, Ss were habituated to either a visual or a haptic 14″-perimeter standard stimulus. During Habituation Period Two, groups were subdivided and presented with one of the following stimuli: (a) 14″ visual, (b) 16″ visual, (c) 14″ haptic, or (d) 16″ haptic. The dependent variables were GSR frequency and amplitude, visual fixation time, and touching time. Subjects required more trials to habituate to the different stimulus presented in Habituation Period Two than Ss who received repeated presentations of the same stimulus. GSR frequency and amplitude habituated more consistently than did fixation and touching response measures. The results supported the use of the habituation paradigm for the study of intersensory and intrasensory integration, as well as providing support for extending Sokolov's theory to intersensory functions.