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.     

The effect of change in sequential visual stimuli on GSR adaptation: II,the novel stimulus as a disinhibiting stimulus

GSR records were obtained for 20 Ss presented with a series of 80 stimuli (four lights alternating in apparent random sequence). Records were obtained, also, for 20 Ss in each of two groups, using the same procedure: in Group 1, a tone was substituted for one of the lights, early in the sequence, and in Group 2, it was substituted later in the sequence. The tone, the novel stimulus, produced significant changes in the GSR adaptation patterns of the two groups.     

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.     

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.     

大学生皮肤电反应、MMPI及其关系的初步研究

应用日产Ｓａｎ－ｅｉｌＡ９７Ａ型脑电图机及ＭＭＰＩ（中国版本）对２６名大学生进行了皮肤电反应记录及人格特征的测查。结果表明：（１）普通大学生中皮电基础水平个体差异十分明显。（２）皮电平均每分钟自发波动次数与ＭＭＰＩ中的Ｄ、Ｓｉ、Ｍａｓ、Ｃｎ呈显著正相关,与Ｌ、Ｋ呈显著负相关。皮电平均每分钟自发波动幅度与Ｆ、Ｄ、Ｍａｓ呈显著正相关;与Ｌ呈显著负相关。（３）皮电基础水平高组与低组在Ｌ、Ｓｉ、Ｍａｓ之Ｔ分上的差异达显著水平。（４）习惯化倾向差组与优组在Ｋ、Ｓｔ、ＭａｓＴ分的差异有显著意义,差组与中组在Ｓｉ、ＣｎＴ分上有显著性差异。（５）习惯化倾向差组皮电基础水平较高;优组皮电基础水平较低,两组差异达显著水平。     

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.     

Primacy effect in orienting responses to auditory stimuli of tones and music.

This 25 factorial experiment investigated the primacy effect in the orienting response. The type of stimuli (tone or "music"), stimulus intensities (loud or soft), length of adaptation period (same, 5 or 30 sec; or different, 5 min.), interstimulus intervals (5 or 30 sec.), and sex were studied. College students, 32 males and 32 females were randomly assigned to each group. In the same condition, the tone (or music) was soft (or loud) for 5 sec. (or 30 sec.) in adaptation and was then changed alternately without interruption to loud, soft, etc. (or soft, loud, etc.) for 5 sec. (or 30 sec.). The different condition was identical except for the length of adaptation period in which the stimuli sounded continously for 5 min. Analyses of the GSR manifestation of the orienting responses indicated: (a) an over-all primacy effect with the auditory stimuli and (b) the primacy effect occurred in the 5-sec.-same but not in the 30-sec.-same condition as predicted.     

Observing responses in pigeons

Pigeons were trained on an observing-response procedure in which periods of VR 100 and EXT alternated unpredictably during a white light (mixed stimulus). During VR 100, responses on a food-producing key (the first key) were intermittently reinforced. Responses on the observing key (the second key) produced a green light (positive stimulus) when VR 100 was in effect, and a red light (negative stimulus) for EXT. The birds did not respond on either key during the negative stimulus, but they responded on the food-producing key when the positive stimulus appeared. When observing responses produced the positive or negative stimulus on FR, observing responses were maintained until the FR reached a maximum; beyond this, only food-producing responses occurred. When observing responses did not produce either stimulus, the observing-response rates fell to zero. With prolonged exposure to an FR 20 schedule of observing, observing-response rates during EXT were higher than during VR 100. Chlorpromazine hydrochloride decreased the total response output but markedly increased observing-response rates except when it was administered before sessions of observing response extinction.     

Laterality differences in sensitivity to line orientation as a function of adaptation duration

Since available evidence indicates that the two cerebral hemispheres are differentially sensitive to different types of stimulus information, and that they also utilize different strategies in processing information, is it possible that the two hemispheres are differentially sensitive to adaptation? Three groups of four subjects each were adapted to black and white gratings using three adapting durations: 500, 1,000, and 5,000 msec. Immediately following adaptation, a test grating was presented in either the left or right visual field. The task of the subject was to determine whether the lines of the adapting and test gratings had the same orientation or not. Analysis showed that in the 5,000-msec and 1,000-msec conditions, more errors occurred with left visual field presentations, responses to left visual field presentations took longer, and a bias-free measure showed that subjects were more sensitive to right visual field presentations. For the 500-msec group, there were no apparent differences between left and right visual fields presentations. The results indicate differential effects of adaptation on the two hemispheres, suggesting sensitivity differences between the two halves of the brain.     

Adaptation to altered visual—vestibular feedback: Mechanisms of maintenance and recovery

Adaptation of perceived movement during head motion (apparent concomitant motion, ACM) and the subsequent elimination of adaptation were studied in two experiments. During the adaptation phase of both experiments, subjects performed voluntary 1-Hz head oscillations for 6 min while fixating a stimulus moving either in the same (with) direction as or the opposite (against) direction of head movements. In Experiment 1, ACM adaptation was measured following either a 1- or a 4-min delay after the adaptation phase. Results indicated some loss of adaptation during the additional 3-min delay, demonstrating a tendency of the system linking head and image to return to its preadaptation state following removal of an adaptation stimulus. In Experiment 2, subjects viewed a stimulus after adaptation that appeared to move minimally in the same manner as the adaptation stimulus during 3 min of head oscillations. No loss of adaptation was measured in these subjects between the beginning and the end of the 3-min interval. In another condition, subjects viewed a stimulus that appeared to move alternately in the same direction as and in the opposite direction of the adaptation stimulus during a similar 3-min interval following adaptation. ACM adaptation was substantially reduced during this 3-min interval. These results implicate two mechanisms that operate to either maintain or eliminate ACM adaptation. One is passive and operates in the absence of visual feedback to eliminate the short-term adapted state, and the other responds to postadaptation visual feedback.     

A comparison of the effects of vicariously instigated classical conditioning and direct classical conditioning procedures

Two groups of Ss received either two or 16 paired classical conditioning trials beyond the peak CR. A third group received the same stimuli as in the 16 postpeak condition but in an unpaired and random order. The stimuli in all three groups were delivered directly to S. Subsequently, all three groups, including a fourth which was not given any prior direct classical conditioning, were exposed to vicariously instigated classical conditioning. This consisted of havingS observe someone (model) employed byE who received the same CS as was delivered during direct conditioning. The CS was paired with the feigned arm movement of the model, simulating a reaction to shock. This vicarious classical conditioning procedure when compared to direct classical conditioning resulted in smaller GSR magnitudes for both the CRs and UCRs. Previous experience with direct classical conditioning seems to have had an attenuating effect on GSR magnitude during the vicarious situation. A postexperimental questionnaire tended to support the results, and the relationship between the present study and current classical conditioning theory is discussed.     

Transfer tests of stimulus value in concurrent chains

We report two experiments that use transfer tests to investigate whether in concurrent chains the value of a terminal-link stimulus is affected by the alternate terminal link. In Experiment 1, two groups of pigeons were trained on multiple concurrent-chains schedules in which switching between the schedules was via pecking a changeover key. For one group, the terminal links were fixed-interval 8 s versus fixed-interval 16 s in one component and fixed-interval 16 s versus fixed-interval 32 s in the other component. For a second group, the terminal links were variable-interval 10 s versus variable-interval 20 s in one component and variable-interval 20 s versus variable-interval 40 s in the other. After sufficient baseline training had been given so that performances had stabilized, transfer tests were conducted in which the two chains with equal terminal-link schedules were presented together as a new concurrent pair. For 6 of the 7 subjects, initial-link responding changed fairly rapidly during the test in the manner predicted if the values of the terminal links were equal. In Experiment 2, pigeons were trained on multiple concurrent chains using a two-key procedure, and the terminal links were the same variable-interval schedules as in Experiment 1. After baseline training, transfer tests were conducted that assessed (a) the relative reinforcing strength of the terminal-link stimuli in a novel initial-link situation and (b) the relative ability of those stimuli to evoke responding. The data from the reinforcing strength test were consistent with those from Experiment 1, but those from the evocation strength test were not. Although this discrepancy shows that responding in transfer tests is not solely a function of stimulus value, the results from both experiments suggest, overall, that value is determined by the stimulus—reinforcer relation independently of the alternative terminal link.     

Informational and neural adaptation curves are asynchronous.

Norwich's entropy theory of perception (plus a few additional assumptions) suggests the existence of an "infromational adaptation curves" (change in stimulus equivocation with stimulus duration) for suprathreshold prothetic stimuli that is synchronous with the "neural adaptation curve" (change in firing rate with stimulus duration) observed for sensory neurons. Five experiments are reported in which informational adaptation curves were measured for auditory and visual stimuli by having subjects make absolute identifications of suprathreshold sound or light intenstiies of various durations. Information transmissions for the shortest duration stimuli (1 and 5 msec, respectively, for light and sound) were surprisingly large (small equivocations), indicating that intensity information is acquired very rapidly by the whole organism. The equations of entropy theory were fitted to adaptation data for peripheral sensory neurons (spiral ganglion cells and retinal ganglion cells) and were compared to the informational adaptation curves. It was found that informational adaptation occurred more rapidly than neural adaptation. That is, the two types of adaptation process are asynchronous. However, for both audition and vision, the total amount of information mediated by the adaptation process (channel capacity) was about the same for both types of processes (2.03 bits vs. 2.1 bits per stimulus for sound intensity; 1.3 vs. 2.0 bits per stimulus for light intensity). Faster acquisition could be accomplished in the whole organism through convergent neural circuits that increase sampling rate by pooling the samples taken by individual receptor systems.     

Visuomotor adaptation in normal aging

Visuomotor adaptation to a gradual or sudden screen cursor rotation was investigated in healthy young and elderly subjects. Both age groups were equally divided into two subgroups; one subgroup was exposed to 11.25° step increments of visual feedback rotation, every 45 trials (up to a total of 90°), whereas a second subgroup was subjected to 90° rotation from the onset of exposure. Participants performed discrete, horizontal hand movements to virtual targets in four randomized directions. Targets appeared on a computer screen in front of them, and a board prevented vision of the hand at all times. Differential effects of aging on visuomotor adaptation were found, depending on the time course of the visual distortion. In both age groups, early exposure to the sudden visual feedback distortion resulted in typical spiral-like trajectories, which became straighter by late exposure. However, the final adaptation level was reduced in the aged group, although the aftereffects were similar. When subjects were exposed to the gradual distortion, no statistically significant differences in measures of adaptation with advancing age were found. In this case, both age groups appeared to adapt equally. However, after removal of the distortion, elderly subjects showed reduced aftereffects as compared with the young group. These findings suggest differential effects of aging on adaptation to gradual versus sudden visual feedback distortions, and may help to explain the conflicting results obtained in previous visuomotor adaptation studies.     

An attentional-adaptation account of spatial negative priming: Evidence from event-related potentials

Negative priming (NP) refers to a slower response to a target stimulus if it has been previously ignored. To examine theoretical accounts of spatial NP, we recorded behavioral measures and event-related potentials (ERPs) in a target localization task. A target and distractor briefly appeared, and the participant pressed a key corresponding to the target’s location. The probability of the distractor appearing in each of four locations varied, whereas the target appeared with equal probabilities in all locations. We found that response times (RTs) were fastest when the prime distractor appeared in its most probable (frequent) location and when the prime target appeared in the location that never contained a distractor. Moreover, NP effects varied as a function of location: They were smallest when targets followed distractors in the frequent distractor location—a finding not predicted by episodic-retrieval or suppression accounts of NP. The ERP results showed that the P2, an ERP component associated with attentional orientation, was smaller in prime displays when the distractor appeared in its frequent location. Moreover, no differences were apparent between negative-prime and control trials in the N2, which is associated with suppression processes, nor in the P3, which is associated with episodic retrieval processes. These results indicate that the spatial NP effect is caused by both short- and long-term adaptation in preferences based on the history of inspecting unsuccessful locations. This article is dedicated to the memory of Edward E. Smith, and we indicate how this study was inspired by his research career.     

Hippocampal lesions attenuate latent inhibition and the decline of the orienting response in rats

Two experiments using rats assessed the effect of dorsal hippocampal lesions on the orienting response (OR) elicited by a discrete light and on the subsequent associability of that light. In both experiments subjects received extensive nonreinforced exposure to the light, and it was found that the decline in the OR evident in sham-operated animals was severely attenuated by hippocampal lesions. Subsequently the light was paired with condensed milk in Experiment 1, and it was found that conditioning was faster in the lesioned than in the sham-operated group. Experiment 2 used a conditioned inhibition procedure whereby the light was presented in a nonreinforced compound with a tone which, when presented alone, acted as a signal for condensed milk. Again this discrimination was mastered more rapidly by lesioned animals. Relevant control groups indicated no differences between lesioned and sham-operated animals in learning about a novel light. Thus, hippocampal lesions influence both the loss of associability of a stimulus and the decline in the OR it elicits, which, in turn, suggests that the OR acts as an index of stimulus associability.     

Informational and neural adaptation curves are asynchronous

Norwich’s entropy theory of perception (plus a few additional assumptions) suggests the existence of an “informational adaptation curve” (change in stimulus equivocation with stimulus duration) for suprathreshold prothetic stimuli that is synchronous with the “neural adaptation curve” (change in firing rate with stimulus duration) observed for sensory neurons. Five experiments are reported in which informational adaptation curves were measured for auditory and visual stimuli by having subjects make absolute identifications of suprathreshold sound or light intensities of various durations. Information transmissions for the shortest duration stimuli (1 and 5 msec, respectively, for light and sound) were surprisingly large (small equivocations), indicating that intensity information is acquired very rapidly by the whole organism. The equations of entropy theory were fitted to adaptation data for peripheral sensory neurons (spiral ganglion cells and retinal ganglion cells) and were compared to the informational adaptation curves. It was found that informational adaptation occurred more rapidly than neural adaptation. That is, the two types of adaptation process are asynchronous. However, for both audition and vision, the total amount of information mediated by the adaptation process (channel capacity) was-about the same for both types of processes (2.03 bits vs. 2.1 bits per stimulus for sound intensity; 1.3 vs. 2.0 bits per stimulus for light intensity). Faster acquisition could be accomplished in the whole organism through convergent neural circuits that increase sampling, rate-by pooling the samples taken by individual receptor systems     

Effect of response task on taste adaptation

Two experiments studied whether subjects reported complete adaptation of a taste sensation. Three tasks were chosen based on their use in other laboratories: hand lowering to connote stimulus absence, magnitude estimation, and cross-adaptation of a brief stimulus following a prolonged stimulus. In the first experiment, different groups of 9 subjects received the three different tasks; in the second experiment, all 20 subjects received all three tasks. In both experiments, subjects failed to demonstrate complete taste adaptation in at least 50% of adaptation trials. Response task did affect the likelihood of observing complete taste adaptation.     

Generalization of extinguished skin conductance responding in human fear conditioning

In a human fear conditioning paradigm using the skin conductance response (SCR), participants were assigned to two groups. Following identical acquisition, group ABA (n = 16) was extinguished to a generalization stimulus (GS), whereas group AAB (n = 20) was extinguished to the conditioned stimulus (CS). At test, presenting the CS in group ABA yielded a strongly recovered SCR. Presenting the GS in group AAB, on the other hand, did not disrupt the effects of extinction. We conclude that extinguishing the CS (group AAB) is an efficient strategy to overcome the stimulus specificity of extinction observed otherwise (group ABA). Clinical implications are discussed.