On the discriminability of stimulus duration.

The performance of pigeons trained to detect differences in the duration of stimuli was analysed using a matching model of signal detection. Two white stimuli, S1 and S2, differing in duration, were arranged with equal probability on the center key of a three-key chamber. S1 was systematically varied from 5 seconds to 25 seconds while S2 remained constant at 30 seconds. On completion of the center-key stimulus, a peck on the center key turned on the two red side keys. A left-key response was "correct" when S1 had been in effect on the center key and a right-key response was "correct" on S2 trials. A correct response produced a 3-second magazine light accompanied intermittently by food. Incorrect responses produced 3-second blackouts. Detection performance was measured under two procedures. In the first, the obtained reinforcement ratio was uncontrolled by allowing the number of food reinforcements obtained for correct left- and right-key responses to vary as the stimuli were changed. In the second procedure, the presentation of food reinforcement was controlled by holding the obtained reinforcement ratio constant. Discriminability changed as a function of stimulus differences under both procedures. No such trend was found in response bias.     

Reinforcer control and human signal-detection performance

Eight humans participated in a two-choice signal-detection task in which stimulus disparity was varied over four levels. Two procedures arranged asymmetrical numbers of reinforcers received for correct left- and right-key responses (the reinforcer ratio). The controlled procedure ensured that the obtained reinforcer ratio remained constant over changes in stimulus disparity, irrespective of subjects' performances. In the uncontrolled procedure, the asymmetrical reinforcer ratio could covary with subjects' performances. The receiver operating characteristic (ROC) patterns obtained from the controlled procedure approximated isobias functions predicted by criterion location measures of bias. The uncontrolled procedure produced variable ROC patterns that were somewhat like the isobias predictions made by likelihood ratio measures of bias; however, the obtained reinforcer ratio became more extreme as discriminability decreased. The obtained pattern of bias was directly related to the obtained reinforcer ratio. This research indicates that criterion location measures seem to be preferable indices of response bias.     

The interaction of stimulus and reinforcer control in complex temporal discrimination.

Six pigeons were trained in a discrete-trials signal-detection procedure to discriminate between a fixed-duration stimulus (5 s or 20 s) and a set of variable durations ranging from 2.5 s to 57.5 s in steps of 5 s. For each fixed-duration stimulus, the ratio of reinforcer frequencies contingent upon reporting the fixed versus the variable stimulus was systematically manipulated. Detection performance was well controlled by both the stimulus value and the reinforcer ratio. Both the discriminability between the fixed duration and the set of variable durations, and the discriminability between the fixed duration and each of the variable durations, were independent of the reinforcer-frequency ratio when discriminability was measured as log d. The sensitivity of response bias to reinforcement-ratio changes was independent of the value of the fixed duration, but was not independent of the discriminability of the variable durations from the fixed durations. Under current models, discriminability measures in complex temporal discrimination may be independent of biasing manipulations, but bias measures are not independent of stimulus values.     

New objects dominate luminance transients in setting attentional priority.

Both the sudden appearance of an object and sudden changes in existing object features influence priority in visual search. However, direct comparisons of these influences have not been made under controlled conditions. In 5 visual search experiments, new object onsets were compared directly with changes in the luminance of old objects. Factors included the luminance contrast of items against the background, the magnitude of luminance change, and the probability that these changes were associated with the target item. New objects were consistently more effective in guiding search, such that a new item with very low luminance contrast was equivalent to an old item undergoing a large change in luminance. An important exception was an old item changing in contrast and polarity, which was as effective as the appearance of a new object. This indicates that search priority is biased toward object rather than situational changes.     

When do luminance changes capture attention?

In two experiments, we examined the ability of task-irrelevant changes in luminance to capture attention in an irrelevant singleton search. By using uniform increment and decrement arrays, we were able to create changes of the same absolute magnitude, but resulting in a singleton with either higher or lower contrast magnitude, relative to other elements in the search array. A condition where a singleton changed contrast polarity without a concomitant change in the overall contrast magnitude was also included. It was found that only luminance changes resulting in a singleton having increased contrast (or saliency) were effective in capturing attention. In addition, no attentional capture was observed when the irrelevant singleton was characterized by the equivalent amount of static luminance differences, suggesting a unique attentional prioritization of luminance changes that increase singleton saliency.     

Acquisition of lever-press responding in rats with delayed reinforcement: A comparison of three procedures

The present study examined the acquisition of lever pressing in rats under three procedures in which food delivery was delayed by 4, 8, and 16 seconds relative to the response. Under the nonresetting delay procedure, food followed the response selected for reinforcement after a specified interval elapsed; responses during this interval had no programmed effect. Under the resetting procedure, the response selected for reinforcement initiated an interval to food delivery that was reset by each subsequent response. Under the stacked delay procedure, every response programmed delivery of food t seconds after its occurrence. Two control groups were studied, one that received food immediately after each lever press and another that never received food. With the exception of the group that did not receive food, responding was established with every procedure at every delay value without autoshaping or shaping. Although responding was established under the resetting delay procedure, response rates were generally not as high as under the other two procedures. These findings support the results of other recent investigations in demonstrating that a response not previously reinforced can be brought to strength by delayed reinforcement in the absence of explicit training.     

Wavelength generalization and discrimination in the pigeon

This three-part study describes wavelength generalization gradients around a series of training wavelengths ranging from 480 to 645 om. Luminance was controlled for the pigeon’s spectral sensitivity. The response measure was probability of keypecking during a 2-sec stimulus presentation. Both an extinction procedure, where stimulus wavelengths occurred in 15-nm steps, and a maintained discrimination procedure, where step size was 2 to 4 nm, were used to obtain gradients. During a portion of the maintained discrimination procedure, new luminances were introduced, so that the effect of luminance level on gradient slope could be examined. Comparison of the resulting functions across training wavelengths revealed: (1) consistent differences in gradient slope in different spectral regions and (2) an increase in slope with luminance increase. The findings are related to recent electroretinographic wavelength contrast data and to psychophysical measures of wavelength discriminability.     

The bisection of a brightness interval by pigeons

Pigeons were trained on a discrete trials, successive discrimination procedure, in which the stimuli were two luminance values on the center key. Behavior was maintained by 25% reinforcement of correct responses on two side-keys. During occasional test trials the luminance of the center key was maintained at one of a number of values, intermediate to those of the two training stimuli, and a function relating the relative frequency of responses on the two side keys to stimulus intensity was obtained. The intersection of this function with the 50% line provided an estimate of the bisection point. Since no bisection point occurred below the geometric mean of the interval, the results were not consistent with a logarithmic scale of brightness but fitted the general mean theorem with an exponent of 0.24. With continued testing, the performance of individual subjects oscillated in an irregular manner about the mean bisection point. The relative stability of the test behavior and the absence of context effects indicated that the method was suitable as a general procedure for measuring stimulus distances.     

Choice with a fixed requirement for food, and the generality of the matching relation

Pigeons were trained on choice procedures in which responses on each of two keys were reinforced probabilistically, but only after a schedule requirement had been met. Under one arrangement, a fixed-interval choice procedure was used in which responses were not reinforced until the interval was over; then a response on one key would be reinforced, with the effective key changing irregularly from interval to interval. Under a second, fixed-ratio choice procedure, responses on either key counted towards completion of the ratio and then, once the ratio had been completed, a response on the probabilistically selected key would produce food. In one experiment, the schedule requirements were varied for both fixed-interval and fixed-ratio schedules. In the second experiment, relative reinforcement rate was varied. And in a third experiment, the duration of an intertrial interval separating choices was varied. The results for 11 pigeons across all three experiments indicate that there were often large deviations between relative response rates and relative reinforcement rates. Overall performance measures were characterized by a great deal of variability across conditions. More detailed measures of choice across the schedule requirement were also quite variable across conditions. In spite of this variability, performance was consistent across conditions in its efficiency of producing food. The absence of matching of behavior allocation to reinforcement rate indicates an important difference between the present procedures and other choice procedures; that difference raises questions about the specific conditions that lead to matching as an outcome.     

STIMULUS EFFECTS ON LOCAL PREFERENCE: STIMULUS—RESPONSE CONTINGENCIES,STIMULUS—FOOD PAIRING,AND STIMULUS—FOOD CORRELATION

Four pigeons were trained in a procedure in which concurrent‐schedule food ratios changed unpredictably across seven unsignaled components after 10 food deliveries. Additional green‐key stimulus presentations also occurred on the two alternatives, sometimes in the same ratio as the component food ratio, and sometimes in the inverse ratio. In eight experimental conditions, we varied the contingencies surrounding these additional stimuli: In two conditions, stimulus onset and offset were noncontingent; in another two, stimulus onset was noncontingent, and offset was response contingent. In four conditions, both stimulus onset and offset were contingent, and in two of these conditions the stimulus was simultaneously paired with food delivery. Sensitivity to component food ratios was significantly higher when stimulus onset was response contingent compared to when it was noncontingent. Choice changes following food delivery were similar in all eight conditions. Choice changes following stimuli were smaller than those following food, and directionally were completely determined by the food‐ratio:stimulus‐ratio correlation, not by the stimulus contingency nor by whether the stimulus was paired with food or not. These results support the idea that conditional reinforcers may best be viewed as signals for next‐food location rather than as stimuli that have acquired hedonic value, at least when the signals are differential with respect to future conditions.     

Combined-stimulus control as a function of the response rate controlled by the absence of the single stimuli

Rat's bar-press responses were maintained at moderate rates during separate presentations of light and tone by separate but concurrent variable-interval schedules of food and shock presentation. The relative response rate maintained during light-out-no-tone was alternated in four successive phases: in Phases 1 and 3 responding was maintained at a higher rate than that during light and tone alone by a variable-interval food schedule, while in Phases 2 and 4 responding was reduced to a lower rate by a differential-reinforcement-of-other-behavior food schedule. In test presentations of light, tone and a light-plus-tone combination, administered at the end of each phase, the proportion of responses emitted during light-plus-tone was an inverse function of the relative response rate controlled by light-out-no-tone, indicating that the relative training response rate controlled by the absence of the single stimuli determined the control exerted by the combined stimuli. Different relative response rates maintained in training may also be partly responsible for previously observed differences in the form of generalization gradients following the establishment of multi-stimulus control.     

Towards a behavioral theory of bias in signal detection

A behavioral model for performance on signal-detection tasks is presented. It is based on a relation between response and reinforcement ratios which has been derived from both animal and human research on the distribution of behavior between concurrently available schedules of reinforcement. This model establishes the ratio of obtained reinforcements for the choice responses, and not the probability of stimulus presentation, as the effective biaser in signal-detection research. Furthermore, experimental procedures which do not control the obtained reinforcement ratio are shown to give rise to unstable bias contours. Isobias contours, on the other hand, arise only from controlled reinforcement-ratio procedures.     

亮度对空间-数字反应编码联合效应的影响

本研究探讨亮度对空间-数字反应编码联合效应（Spatial-Numerical Association of Response Codes,简称SNARC效应）的影响及其机制。通过三个实验设计不同的亮度对比水平,要求被试对阿拉伯数字1~9（5除外）进行奇偶判断。实验一将数字亮度设为最高值255时,结果出现了数字的SNARC效应。实验二将数字的亮度值分别设为255和213时,结果仍存在SNARC效应。实验三将亮度值分别设置为213和42时,数字的SNARC效应却消失了。这些结果表明亮度会激活或抑制数字的空间表征,可能与亮度对比值的高低及所消耗认知资源的多少有关。     

Differential acquisition of conditioned suppression in rats with increased and decreased luminance levels as CS + s

Using a conditioned suppression procedure, it was demonstrated that suppression of responding was substantially enhanced when the CS signaling the occurrence of shock was an increment in luminance level (bright CS), relative to an equivalent decrement in luminance level serving as a signal for shock (dim CS). The results of a pseudoconditioning control procedure illustrated that the differential effectiveness of the bright and dim CSs was dependent upon explicit CS-US pairings. The bright and dim stimuli were found to produce equivalent rates of conditioning when they were used to signal the availability of reinforcing stimuli in an appetitive discrimination procedure. The interpretation considered to be most consistent with the data is associative in nature; rats may be brought into the experimental setting prepared to associate bright light with danger and contraprepared to associate dim light with danger.     

Why pigeons say what they do: reinforcer magnitude and response requirement effects on say responding in say-do correspondence

The effects of reinforcer magnitude and response requirement on pigeons' say choices in an experimental homologue of human say-do correspondence were assessed in two experiments. The procedure was similar to a conditional discrimination procedure except the pigeons chose both a sample stimulus (the say component) and a comparison stimulus that corresponded to it (the do component). Correspondence was trained on red, green, and white key colors before the duration of food presentations following correspondence on each key color (Experiment 1) and the number of key pecks required as the say response on each key color (Experiment 2) were manipulated in an attempt to influence the initial say response. The frequency of say responses on each key color coincided with programmed changes in the duration of food presentations and the key-peck requirements assigned to each key color. Correspondence accuracy remained stable in all conditions, even those in which the say responding occurred primarily on two of the three key colors. Implications for human behavior are discussed.     

RESISTANCE TO CHANGE AND FREQUENCY OF RESPONSE‐DEPENDENT STIMULI UNCORRELATED WITH REINFORCEMENT

Stimuli uncorrelated with reinforcement have been shown to enhance response rates and resistance to disruption; however, the effects of different rates of stimulus presentations have not been assessed. In two experiments, we assessed the effects of adding different rates of response‐dependent brief stimuli uncorrelated with primary reinforcement on relative response rates and resistance to change. In both experiments, pigeons responded on variable‐interval 60‐s schedules of food reinforcement in two components of a multiple schedule, and brief response‐dependent keylight‐color changes were added to one or both components. Although relative response rates were not systematically affected in either experiment, relative resistance to presession feeding and extinction were. In Experiment 1, adding stimuli on a variable‐interval schedule to one component of a multiple schedule either at a low rate (1 per min) for one group or at a high rate (4 per min) for another group similarly increased resistance to disruption in the components with added stimuli. When high and low rates of stimuli were presented across components (i.e., within subjects) in Experiment 2, however, relative resistance to disruption was greater in the component presenting stimuli at a lower rate. These results suggest that stimuli uncorrelated with food reinforcement do not strengthen responding in the same way as primary reinforcers.     

Control by stimulus features during fading.

Sixteen children were given four successive circle-size discrimination problems with luminance as the fading stimulus. Children who were first presented with a difficult size discrimination failed to acquire this discrimination. Those who first received an easy discrimination learned the difficult discrimination. At the end of each 10-trial block, two probe stimuli were presented to monitor any shift in control from luminance to size. One probe was the same size as the positive stimulus but of different luminance; the other was the same luminance but of different size. If, in the course of fading, size and luminance both controlled responding, fading was successful. If luminance alone controlled responding until the end of fading, the size discrimination was not established. Dual control, and thus successful fading, resulted when the target stimuli were very discriminable, or when the target stimuli were subtly different provided that previous fading series had first established less subtle discriminations.     

Effects of signaling on temporal control of behavior in response‐initiated fixed intervals

Behavior and events distributed in time can serve as markers that signal delays to future events. The majority of timing research has focused on how behavior changes as the time to some event, usually food availability, decreases. The primary objective of the two experiments presented here was to assess how behavior changes as time passes between two time markers when the first time marker was manipulated but the second, food delivery, was held constant. Pigeons were exposed to fixed‐interval, response‐initiated fixed‐interval, and signaled response‐initiated fixed‐interval 15‐ and 30‐s schedules of reinforcement. In Experiment 1, first‐response latencies were systematically shorter in the signaled response‐initiated schedules than response‐initiated schedules, suggesting that the first response was a more effective time marker when it was signaled. In Experiment 2, responding in no‐food (i.e. “peak”) trials indicated that timing accuracy was equivalent in the three schedule types. Compared to fixed interval schedules, timing precision was reduced in the signaled response‐initiated schedules and was lowest in response‐initiated schedules. Results from Experiments 1 and 2 coupled with previous research suggest that the overall “informativeness” of a time marker relative to other events and behaviors in the environment may determine its efficacy.     

Elimination of reinforced behavior: intermittent schedules of not-responding

Pigeons' key pecking resulted in food according to either a variable-ratio or a variable-interval schedule. At the same time, food was available for not pecking for a specified time. The required time of not-pecking was segmented into not-responding units, and these units were followed by food according to a fixed-ratio schedule. Both unit duration and the number required were varied. In general, the shorter the time unit or the smaller the ratio, the lower was response rate. When total required not-responding time was constant, but changes in unit duration and the number required altered how the total was achieved, shorter units produced lower rates. Other conditions involved substitution of food delivered independent of responding for the not-responding schedule. With low and moderate total times to food presentation, the not-responding schedule produced lower rates; with the longest times, the response-independent schedule generated less responding. When considered in terms of relative frequency of food presentation available from a source other than pecking, the not-responding schedule reduced rate more effectively than did the response-independent schedule. Comparisons with other research suggested that food presented dependent on not responding compared favorably with punishment as a procedure for reducing response rate. Transient effects differed. Although punishment temporarily depresses rate when first imposed and temporarily enhances it when first removed, food given for not responding quickly generated steady-state rates.     

The reinforcement of four interresponse times in a two-alternative situation

Pigeons pecked for food in a two-key procedure. A concurrent variable-interval variable-interval schedule of reinforcement for two classes of interresponse times was arranged on each key. A visual stimulus set the occasion for potential reinforcement of the four operant classes: shorter and longer interresponse times on left and right keys. In Exp. I, the relative frequency of respones on a key equalled the relative frequency of reinforcement on that key. In Exp. II, the relative frequency of an interresponse time equalled the relative reciprocal of its length. In Exp. III, the relative frequency of an interresponse time was a monotonically increasing function of its relative frequency of reinforcement. These functions relating the relative frequency of an interresponse time to its relative length and to its relative frequency of reinforcement were the same as if there had been no second key. Also, the distribution of responses between keys was independent of the relative frequency of an interresponse time on either key. Experiment IV replicated Exp. I except that choices between keys were controlled by a stimulus that signalled the availability of reinforcement on the right key. A comparison of Exp. I and IV suggested that the relative frequency of an interresponse time on one key generally was independent of behavior on the other key, but that the number of responses per minute on a key did depend on behavior on the other key.