Effects of chlorpromazine on fixed-ratio responding: modification by fixed-interval discriminative stimuli.

Effects of chlorpromazine (1 to 100 mg/kg) were assessed on two pigeons' responding under various modifications of a multiple schedule of food delivery. During a fixed-interval component, the first response after 5 min produced food; during the subsequent, fixed-ratio component, the 30th response produced food. Modifications of the schedule entailed changes in stimulus conditions imposed during the fixed-ratio component that did not systematically alter characteristics of performance under non-drug conditions. In the first phase of the experiment, distinctive visual stimuli were correlated with each schedule component (conventional multiple schedule); chlorpromazine produced small decreases in fixed-ratio responding (20% at 30 mg/kg). When each response during the fixed-ratio component produced the stimulus correlated with the fixed-interval schedule (fixed-interval discriminative stimulus) for 1.2 s, effects of chlorpromazine were not different from those under the conventional multiple schedule. Chlorpromazine produced greater decreases in fixed-ratio responding (55% at 30 mg/kg) when either the first response of each fixed ratio changed the stimulus correlated with the fixed-ratio schedule to the fixed-interval discriminative stimulus for the remainder of the fixed-ratio component, or when the fixed-interval discriminative stimulus was presented independently of responding according to a matched temporal sequence. When the fixed-interval discriminative stimulus was present continuously during the fixed-ratio component (mixed schedule), chlorpromazine produced even more substantial decreases in fixed-ratio responding (greater than 80% at 30 mg/kg). Effects of chlorpromazine on fixed-interval responding were also modified by the schedules of fixed-interval discriminative stimulus presentation. The effects of chlorpromazine were a joint function of the stimuli prevailing during the multiple schedule and the degree to which responding influenced these stimuli.     

Relational and absolute stimulus learning by monkeys in a memory task.

Three experiments showed stimulus control by either the absolute properties of probe stimuli, relational properties of the probe-list relationship, or both in a serial probe recognition memory task in which a four-item memory list was followed by a single probe (test) item. In Experiment 1, 3 rhesus monkeys received 39 to 75 repetitions of the same 24-trial stimulus sequence. Special tests showed stimulus control by the absolute properties of the probe stimuli. Retention of previous relational control was demonstrated by the good transfer (83%) to novel list and probe stimuli at the beginning of Experiment 2. During Experiment 2, control by absolute properties of the probe stimuli gradually reoccurred. Only a small measure of control by list stimuli could be detected or promoted. In Experiment 3, 4 monkeys were shown to have largely lost their ability to perform on the basis of the list-probe relationship, and were performing primarily on the basis of the absolute properties of the probe stimuli. Over the next 15 weeks, these monkeys were transferred to new stimuli at the beginning of each week. Control by the relational aspects of the task gradually returned. As transfer performance increased, control by the absolute properties of the probe stimuli was eliminated. The results are discussed in terms of stimulus control and performance strategies used by the monkeys.     

封闭性知觉在大范围优先性中的特殊性

本文研究当封闭性作为被试分辨的图形性质时,空间位置不确定性和视野位置对大范围优先性有何影响。实验发现：（１）无论复合刺激呈现在视野的中央或外周．分辨复合刺激的整体性质的反应时（ＲＴ）比分辨局部性质的ＲＴ短,整体性质对分辨局部性质的反应有较强的干扰作用。相反,局部性质对分辨整体性质的反应的影响较小;（２）刺激位置的不确定对大范围优先性没有显著影响;（３）与周边刺激相比,分辨视野中央的复合刺激的ＲＴ较短,但整体性质的ＲＴ优势和对局部性质的干扰作用,不受刺激在视野中的位置的影响。这些实验结果揭示了封闭性知觉在大范围优先性中的特殊性。     

Facial reactions to different emotionally relevant stimuli

Facial EMG activity was measured from the Corrugator supercilii and the Zygomatic major muscle regions while 48 subjects were exposed to pictures of angry and happy facial expressions, snakes and flowers as well as low and high preference nature scenes. The valency perspective predicted that facial reactions should be related to the intensity of the positive and the negative valency of stimuli. The mimicking behavior approach predicted that facial reactions should only be reflected as a mimicking response to the facial stimuli, whereas the evolutionary:biological perspective predicted that the most clearcut positive and negative facial reactions should be evoked by facial stimuli and by snakes. In support of the latter perspective, the present results showed that angry faces and snakes evoked the most distinct Corrugator supercilii muscle response, whereas happy faces evoked the largest Zygomatic major muscle response.     

Selective sensitivity of schedule-induced activity to an operant suppression contingency.

The sensitivity of pigeons' schedule-induced activity to operant consequences was studied in two experiments. During a 30-s interval between food presentations, a keylight stimulus brightened incrementally. Stable terminal key pecking and interim locomotor activity developed. An operant "setback" contingency was applied to activity. The contingency arranged for locomotor movements (detected by a nine-panel floorboard) to be followed by a resetting of the keylight brightness to a dimmer value and a 1-s delay of reinforcement (for individual responses). Experiment 1 showed that activity patterns were highly sensitive to their operant consequences. Accompanying key-peck rates were only transiently affected. In Experiment 2, the setback contingency was imposed during restricted portions of the trial, and differential operant control of activity was demonstrated. However, birds in this study produced higher rates of key pecking as activity rates were reduced. These results suggest that although schedule-induced activity arises in response to the temporal arrangement of stimulus events, this behavior may retain considerable sensitivity to response-consequence relations.     

"Turning back the clock" on serial-stimulus sign tracking.

Two experiments examined the effects of a negative (setback) response contingency on key pecking engendered by a changing light-intensity stimulus clock (ramp stimulus) signaling fixed-time 30-s food deliveries. The response contingency specified that responses would immediately decrease the light-intensity value, and, because food was delivered only after the highest intensity value was presented, would delay food delivery by 1 s for each response. The first experiment examined the acquisition and maintenance of responding for a group trained with the contingency in effect and for a group trained on a response-independent schedule with the ramp stimulus prior to introduction of the contingency. The first group acquired low rates of key pecking, and, after considerable exposure to the contingency, those rates were reduced to low levels. The rates of responding for the second group were reduced very rapidly (within four to five trials) after introduction of the setback contingency. For both groups, rates of responding increased for all but 1 bird when the contingency was removed. A second experiment compared the separate effects of each part of the response contingency. One group was exposed only to the stimulus setback (stimulus only), and a second group was exposed only to the delay of the reinforcer (delay only). The stimulus-only group's rates of responding were immediately reduced to moderate levels, but for most of the birds, these rates recovered quickly when the contingency was removed. The delay-only groups's rates decreased after several trials, to very low levels, and recovery of responding took several sessions once the contingency was removed. The results suggest that (a) sign-tracking behavior elicited by an added clock stimulus may be reduced rapidly and persistently when a setback contingency is imposed, and (b) the success of the contingency is due both to response-dependent stimulus change and response-dependent alterations in the frequency of food delivery. The operation of the contingency is compared with the effects of secondary reinforcement and punishment procedures.     

A functional analysis of another individual's behavior as discriminative stimulus for a monkey.

Key presses of 1 monkey (called the performer) became the basis upon which a 2nd monkey (called the judge) solved conditional-discrimination tasks. First, the performer was trained to press one of two colored choice keys (red or green) depending on the location of a white light in her chamber. The performer's key-pressing behavior was brought under the control of the experimenter by this procedure. Subsequently, the judge was trained to discriminate the performer's key-pressing behavior. In Experiment 1, the judge had to press Key 1 when the performer pressed the red choice key and Key 2 when the performer pressed the green choice key. In Experiment 2, a sample key was introduced. The judge had to press Key 1 when the performer pressed the same colored choice key as the sample; the judge had to press Key 2 when the performer pressed the different colored choice key. In both experiments, the judge was required to attend to the behavior of the performer. It was shown that the performer's behavior served as a discriminative stimulus for the judge's responses in a conditional-discrimination task.     

Perceived unpleasantness and facial reactions to auditory stimuli

This study examined whether facial electromyographic (EMG) reactions differentiate between identical tone stimuli which subjects perceive as differently unpleasant. Subjects were repeatedly exposed to a 1000 Hz 75 dB tone stimulus while their facial EMG from the corrugator and zygomatic muscle regions were measured. Skin conductance and heart rate responses were also measured. The subjects rated the unpleasantness of the stimulus and based on these ratings they were divided into two groups, High and Low in perceived unpleasantness. As predicted the facial EMG activity reflected the perceived unpleasantness. That is, the High group but not the Low group reacted with an increased corrugator response. The autonomic data, on the other hand, did not differ between groups. The results are consistent with the proposition that the facial muscles function as a readout system for emotional reactions and that facial muscle activity is intimately related to the experiential level of the emotional response system.     

Polydipsia induced in rats by second-order schedules of reinforcement.

Three rats were exposed to a second-order schedule in which fixed-interval components ended either with food or with a brief stimulus that was never paired with food. Food and the brief stimulus occurred in a random sequence (variable-ratio 2 overall schedule). Another three rats were exposed to a similar second-order schedule, the only difference being that the food or the stimulus was presented independently of operant behavior (fixed-time components). The three rats exposed to the fixed-interval components licked at a water spout after each food presentation. These rats also licked in the intervals after the brief stimulus. Although the discriminative properties of food and of the brief stimulus were identical in relation to subsequent reinforcement, licking after the stimulus was less than after food. The three rats exposed to the second-order schedules with fixed-time components also licked at the water spout after food, but these rats did not lick consistently after brief stimulus presentations.     

Fading and errorless transfer in successive discriminations

A successive discrimination between red positive and green negative stimuli was established with pigeon subjects. Then, lines with different angular orientations were superimposed on one of the colors to form compound stimuli. Finally, either the colored element of the positive compound, the colored element of the negative compound, or both colored elements together, were gradually attenuated. Before each attenuation, the line elements were presented alone against dark backgrounds as probes to assess the degree to which they had acquired control of responding. When the positive color was attenuated alone or in conjunction with the negative color, angular orientation acquired control of responding in an errorless fashion. Lines, however, did not acquire control when only the negative component was attenuated. These results were interpreted in terms of changes in the predictability of reinforcement by color and line elements during stimulus attenuation. Finally, attenuation of the negative stimulus influenced the number of “dimensions” of the new line stimuli that acquired control of responding. When the positive stimulus was attenuated with the negative, only one dimension of the lines acquired control. When the positive stimulus was attenuated without the negative, however, more than one dimension of the lines acquired control of responding. These results were interpreted in terms of how errorless performance can be maintained while an organism attends to different dimensions of the new stimuli.