Distortions of temporal integration and perceived order caused by the interplay between stimulus contrast and duration

Stimulus contrast and duration effects on visual temporal integration and order judgment were examined in a unified paradigm. Stimulus onset asynchrony was governed by the duration of the first stimulus in Experiment 1, and by the interstimulus interval in Experiment 2. In Experiment 1, integration and order uncertainty increased when a low contrast stimulus followed a high contrast stimulus, but only when the second stimulus was 20 or 30 ms. At 10 ms duration of the second stimulus, integration and uncertainty decreased. Temporal order judgments at all durations of the second stimulus were better for a low contrast stimulus following a high contrast one. By contrast, in Experiment 2, a low contrast stimulus following a high contrast stimulus consistently produced higher integration rates, order uncertainty, and lower order accuracy. Contrast and duration thus interacted, breaking correspondence between integration and order perception. The results are interpreted in a tentative conceptual framework.     

A test of the reinforcing properties of stimuli correlated with nonreinforcement

The information hypothesis of conditioned reinforcement predicts that a stimulus that “reduces uncertainty” about the outcome of a trial will acquire reinforcing properties, even when the stimulus reliably predicts nonreinforcement. Four pigeons' key pecks produced one of two 5-sec stimuli with 0.50 probability according to a discriminated variable-interval schedule. One stimulus was followed by reinforcement; a second stimulus was followed by blackout. To the same extent, therefore, both stimuli reduced uncertainty about the possibility that food would arrive at the termination of the schedule interval. When a second key in the chamber was lighted, each peck on it could produce the stimulus preceding reinforcement, the stimulus preceding nonreinforcement, a novel stimulus, or no stimulus, across separate conditions. The stimulus preceding food maintained responding at substantial levels on the second, stimulus-producing, key. Such responding was not maintained by other stimuli. These data, replicated when the stimuli were reversed on the variable-interval schedule, do not support the prediction that uncertainty-reducing stimuli are necessarily conditioned reinforcers.     

Inhibitory control and errorless discrimination learning

Pigeons learned to discriminate between a positive stimulus (white key) and a negative stimulus (red or green key, depending on the subject) via Terrace's fading procedure. Generalization tests, conducted with intermittent reinforcement for key pecking at various wavelengths, yielded minima at the value of the negative stimulus in most “errorless” birds. Terrace's contrary finding of flat gradients in errorless subjects probably resulted from a floor-effect (i.e., virtually zero responding) produced by his extinction-test procedure. The present and other findings do not support Terrace's conclusions that the negative stimulus of an errorless discrimination is behaviorally neutral; inhibition apparently develops to the nonreinforced stimulus even during errorless discrimination learning. A negative correlation between stimulus and reinforcer seems the crucial factor in producing an inhibitory stimulus.     

Second-order schedules: comparison of different procedures for scheduling paired and nonpaired brief stimuli

Pigeons performed on a second-order schedule in which fixed-interval components were maintained under a variable-interval schedule. Completion of each fixed-interval component resulted in a brief-stimulus presentation and/or food. The relation of the brief stimulus and food was varied across conditions. Under some conditions, the brief stimulus was never paired with food. Under other conditions, the brief stimulus was paired with food; three different pairing procedures were used: (a) a response produced the simultaneous onset of the stimulus and food; (b) a response produced the stimulus before food with the stimulus remaining on during food presentation; (c) a response produced the stimulus and the offset of the stimulus was simultaneous with the onset of the food cycle. The various pairing and nonpairing operations all produced similar effects on performance. Under all conditions, response rates were positively accelerated within fixed-interval components. Total response rates and Index of Curvature measures were similar across conditions. In one condition, a blackout was paired with food; with this different stimulus in effect, less curvature resulted. The results suggest that pairing of a stimulus is not a necessary condition for within-component patterning under some second-order schedules.     

Perception of internal elements of compound figures by one-month-old infants

Previous research has shown that infants younger than 2 months frequently concentrate their attention on peripheral or external features of visual stimuli and that they do not appear to process the internal elements of a compound visual stimulus composed of a simple geometric figure enclosed in a larger figure. A visual habituation-dishabituation paradigm was used to determine whether 1-month-old infants would process internal information if the internal elements of the stimulus were patterns often found to be preferred by young infants. Four groups of eight infants each were habituated to a compound stimulus consisting of a square or triangle surrounding a checkerboard or bull's-eye. Following habituation each group was presented with one of four types of stimulus: the identical stimulus (control group), a stimulus differing only in the internal component, a stimulus differing only in the external component, or a stimulus differing in both components. The results of the present study suggest that when the internal element of a compound stimulus is a highly preferred or salient stimulus, the young infant will process information about its characteristics.     

Simple discrimination in stingless bees (Melipona quadrifasciata): Probing for select‐ and reject‐stimulus control

Simple and conditional discrimination training may produce various types of controlling relations. Responses may be controlled primarily by the positive stimulus (select–control relation) or by the negative stimulus (reject–control relation; the subject excludes the negative stimulus and chooses the positive). Bees learn to respond in simple and conditional discriminations. However, no study has searched for reject–control responding in Melipona bees. We trained Melipona quadrifasciata on a simple discrimination task (S+ vs. S‐; e.g., blue vs. yellow) and then probed for stimulus control with two types of probe trials, S+ versus a new stimulus (Select–control probes) and S‐ versus a new stimulus (Reject–control probes). For Group Different, a new‐stimulus color (e.g., white) was used in one type of probe and another color (e.g., black) was used in the other type. For Group Same, a single new‐stimulus color was used in both types of probes. On Select probes, the bees always preferred S+ to the new stimulus. On Reject probes, results were mixed. Depending on the colors used in training and probing, bees responded to both stimuli, and even preferred the S‐. The data suggest no control by the negative function of the S‐ and support the select‐stimulus control hypothesis of responding.     

Visual masking and RSVP reveal neural competition

A test visual stimulus is harder to recognize when another stimulus is presented in close temporal vicinity; presenting stimuli in close spatial vicinity of a test stimulus reduces its visibility; presenting a stimulus to one eye can render invisible another stimulus presented to the other eye; and perceiving one interpretation of an ambiguous image prevents the simultaneous perception of other visual interpretations. A single, neurophysiological theory, which may be called 'neural competition' might explain all these phenomena: when two alternative neural visual representations co-exist in the brain, they compete against each other.     

A Study of Happiness and Unhappiness in the Childhood and Adolescence of Girls in Different Cultures

Experiments were reviewed which dealt with the effect of an auditory cue stimulus on sensitivity to a visual detection stimulus, and vice versa. In most cases the heteromodal cue was temporally varied around the time of occurrence of the detection stimulus.

Different results were reported when a prolonged cue was used (which overlapped the detection stimulus when the onsets of both were not simultaneous) than when a brief-duration cue was used: e.g., in the former case, but not in the latter, sensitivity to the detection stimulus was affected by the intensity of a clearly perceptible heteromodal cue. Es tended to explain the effects of prolonged cue in “neurophysiological-interaction” terms and of brief-duration cue in “attentional” terms. Delta t (difference between times of detection-stimulus and cue onset) was most likely to affect sensitivity to the detection stimulus when marker stimuli reliably informed S when to attend for the detection stimulus, but did not exactly define its time of possible occurrence. A consistent delta-t effect was that a light-cued sound stimulus was best detected when the flash preceded it by 0 to 500 msec.     

Enhanced Latent Inhibition Following Compound Pre-exposure

The influence of non-reinforced exposure to compound stimuli on subsequent appetitive classical conditioning was examined in five experiments with rats as the subjects. Non-reinforced exposure to a visual stimulus retarded subsequent acquisition of conditioned responding relative to a non-pre-exposed condition (latent inhibition). If the target stimulus was pre-exposed in compound with a second (non-target) stimulus, then latent inhibition was abolished. Exposure to the non-target stimulus prior to compound exposure had varying effects on subsequent conditioning to the target: 40 exposures to the non-target stimulus resulted in latent inhibition to the target stimulus that was comparable in magnitude to that observed when the target stimulus was exposed in isolation; 120 exposures to the non-target stimulus enhanced latent inhibition to the target stimulus.     

Using ambiguous plaid stimuli to investigate the influence of immediate prior experience on perception

In a series of three experiments, we used an ambiguous plaid motion stimulus to explore the behavioral and electrophysiological effects of prior stimulus exposures and perceptual states on current awareness. The results showed that prior exposure to a stimulus biased toward one percept led to subsequent suppression of that percept. In contrast, in the absence of stimulus bias, prior perceptual experience can have a facilitative influence. The suppressive effects caused by the prior stimulus were found to transfer to an ambiguous plaid test stimulus rotated 180º relative to the adaptation stimulus, but were abolished if (1) the ambiguous test stimulus was only rotated 90º relative to the adaptation stimulus or (2) the adaptation stimulus was heavily biased toward the component grating percept. Event-related potential recordings were consistent with the involvement of visual cortical areas and suggested that the influence of recent stimulus exposure may involve recruitment of additional brain processes beyond those responsible for initial stimulus encoding. In contrast, the effects of prior and current perceptual experience appeared to depend on similar brain processes. Although the data presented here focus on vision, the work is discussed within the context of data from a parallel series of experiments in audition.     

Asymmetry in infant hemispheric readiness after exposure to a visual stimulus

This experiment assessed whether prior exposure to one visual stimulus could result in differential hemispheric responsiveness to a subsequent visual stimulus. The latency of saccadic orientation to a star‐shaped stimulus in the left or right visual field was assessed for 24 infants (mean age 22 weeks, SD 4.5) after exposure to either an upright or inverted facial pattern in the central visual field. The response to the lateral stimulus was equivalent in either visual field after exposure to the inverted facial pattern, but was significantly slower (p = 0.043) in the LVF (RH) than the RVF (LH) following presentation of the upright facial pattern. The outcome confirms that the processing of one visual stimulus may lead to differential hemispheric readiness to engage with a subsequent visual stimulus.     

An improved technique for monitoring fixation in tachistoscopic tasks

A monocular lens mounted behind a stimulus screen was used to monitor fixation in a tachistoscopic recognition task. This technique was found superior to the often used “sideview technique” and as accurate as the method involving identification of a fixation stimulus. It was found that the “telescope technique” is preferable in those studies where presentation of a fixation stimulus might interfere with recognition or report of the experimental stimulus.     

Iconic memory and visible persistence

There are three senses in which a visual stimulus may be said to persist psychologically for some time after its physical offset. First, neural activity in the visual system evoked by the stimulus may continue after stimulus offset (“neural persistence”). Second, the stimulus may continue to be visible for some time after its offset (“visible persistence”). Finally, information about visual properties of the stimulus may continue to be available to an observer for some time after stimulus offset (“informational persistence”). These three forms of visual persistence are widely assumed to reflect a single underlying process: a decaying visual trace that (1) consists of afteractivity in the visual system, (2) is visible, and (3) is the source of visual information in experiments on decaying visual memory. It is argued here that this assumption is incorrect. Studies of visible persistence are reviewed; seven different techniques that have been used for investigating visible persistence are identified, and it is pointed out that numerous studies using a variety of techniques have demonstrated two fundamental properties of visible persistence: theinverse duration effect (the longer a stimulus lasts, the shorter is its persistence after stimulus offset) and theinverse intensity effect (the more intense the stimulus, the briefer its persistence). Only when stimuli are so intense as to produce afterimages do these two effects fail to occur. Work on neural persistences is briefly reviewed; such persistences exist at the photoreceptor level and at various stages in the visual pathways. It is proposed that visible persistence depends upon both of these types of neural persistence; furthermore, there must be an additional neural locus, since a purely stereoscopic (and hence cortical) form of visible persistence exists. It is argued that informational persistence is defined by the use of the partial report methods introduced by Averbach and Coriell (1961) and Sperling (1960), and the term “iconic memory” is used to describe this form of persistence. Several studies of the effects of stimulus duration and stimulus intensity upon the duration of iconic memory have been carried out. Their results demonstrate that the duration of iconic memory is not inversely related to stimulus duration or stimulus intensity. It follows that informational persistence or iconic memory cannot be identified with visible persistence, since they have fundamentally different properties. One implication of this claim that one cannot investigate iconic memory by tasks that require the subject to make phenomenological judgments about the duration of a visual display. In other words, the so-called “direct methods” for studying iconic memory do not provide information about iconic memory. Another implication is that iconic memory is not intimately tied to processes going on in the visual system (as visible persistence is); provided a stimulus is adequately legible, its physical parameters have little influence upon its iconic memory. The paper concludes by pointing out that there exists an alternative to the usual view of iconic memory as a precategorical sensory buffer. According to this alternative, iconic memory is post-categorical, occurring subsequent to stimulus identification. Here, stimulus identification is considered to be a rapid automatic process which does not require buffer storage, but which provides no information about episodic properties of a visual stimulus. Information about these physical stimulus properties must, in some way, be temporarily attached to a representation of the stimulus in semantic memory; and it is this temporarily attached physical information which constitutes iconic memory.     

3.5~5.5岁儿童在知觉相似与概念冲突情形下的归纳推理

了探讨儿童是基于知觉相似的还是基于概念的进行归纳推理的,利用儿童较为熟悉的材料,设计了一种知觉相似与概念冲突的情形,并在4种不同的信息提示条件下,测试了总共275名3.5岁、4.5岁和5.5岁儿童的归纳推理。实验结果显示,在预备实验中,3.5岁的儿童已经能够排除无关刺激要么基于知觉相似要么基于概念进行归纳推理,但二者没有显著差异;在正式实验中,在4种任务条件下,3.5岁的儿童的情况基本与预备实验相同,而4.5岁和5.5岁的儿童则更倾向于基于概念进行归纳推理,这表明儿童的归纳推理可能的确经历了从依据知觉相似到依据概念关系的转变,但发生转变的年龄应该不是在7~8岁,而是在4岁之前     

The effect of overtraining on behavioral contrast and the peak-shift

Following initial discrimination training between two wavelength stimuli and a subsequent generalization test to the wavelength dimension, Group 1 was “overtrained” for 105 days on the original discrimination. Group 2 was “overtrained” with the original positive stimulus and a new negative stimulus, a white line. Group 3 was “overtrained” with the original negative stimulus and a new positive stimulus, the white line. Each 15 days of extended training were followed by a wavelength generalization test similar to the first test. The results suggest that there is no consistent relationship between the response rate in positive stimulus immediately before the generalization test and whether or not a peak shift occurs during the test.     

The effects of self-monitoring and self-reported consistency on the consistency of personality judgments made by strangers and intimates

How consistent are strangers' and intimates' judgments of stimulus people's personalities, and how is this interjudge consistency affected by stimulus persons' assessed self-monitoring and self-reported behavioral consistency? To answer these questions, 38 stimulus subjects rated themselves on the personality dimensions of extraversion and anxiety and also rated their cross-situational consistency on these dimensions. Strangers, friends, mothers, and fathers of stimulus persons also rated them on extraversion and anxiety. The results indicated that: For judgments of anxiety there was lower interjudge consistency for high than for low self-monitoring stimulus subjects. For judgments of extraversion there was no difference in interjudge consistency for low and high self-monitoring stimulus subjects. The results also showed that anxiety was a more “private” trait in that intimates' but not strangers' judgments correlated with stimulus subjects' self-reported anxiety (r = .50 and r = .11, respectively), while extraversion was a more “public” trait in that both intimates' and strangers' judgments correlated with stimulus subjects' self-reported extraversion (r = .42 and r = .51, respectively). These results suggest that self-monitoring of stimulus persons affects interjudge consistency of peroonality judgments particularly for “private” traits such as anxiety, which are most subject to expressive control and inhibition.     

Localizing the first position of a moving stimulus: The Fröhlich effect and an attention-shifting explanation

When subjects are asked to determine where a fast-moving stimulus enters a window, they typically do not localize the stimulus at the edge, but at some later position within that window (Fröhlich effect). We report five experiments that explored this illusion. An attentional account is tested, assuming that the entrance of the stimulus in the window initiates a focus shift toward it. While this shift is under way, the stimulus moves into the window. Because the first phenomenal (i.e., explicitly reportable) representation of the stimulus will not be available before the end of the focus shift, the stimulus is perceived at some later position. In Experiment 1, we established the Fröhlich effect and showed that its size depends on stimulus parameters such as movement speed and movement direction. In Experiments 2 and 3, we examined the influence of eye movements and tested whether the effect changed when the stimuli were presented within a structural background or when they started from different eccentricities. In Experiments 4 and 5, specific predictions from the attentional model were tested: In Experiment 4 we showed that the processing of the moving stimulus benefits from a preceding peripheral cue indicating the starting position of the subsequent movement, which induces a preliminary focus shift to the position where the moving stimulus would appear. As a consequence the Fröhlich effect was reduced. Using a detection task in Experiment 5, we showed that feature information about the moving stimulus is lost when it falls into the critical interval of the attention shift. In conclusion, the present attentional account shows that selection mechanisms are not exclusively space based; rather, they can establish a spatial representation that is also used for perceptual judgment—that is, selection mechanisms can bespace establishing as well.     

Conditioned punishment

Responses of pigeons were maintained by a VI schedule of food reinforcement. Conditioned punishment was programmed by having these responses concurrently produce an originally neutral stimulus. The effectiveness of this response-contingent stimulus was maintained by infrequent and prearranged stimulus-shock pairings delivered independently of responses. This conditioned punishment procedure reduced the overall response rate as long as the procedure was in effect. The extent and durability of the reduction was a function of the intensity of the shock that was paired with the stimulus. Analysis of the reduction in the overall response rate revealed: (1) a reduction of responses occurring in the absence of the response-contingent stimulus, which was designated as a “punishing” effect, and (2) a reduction of responses during the response-contingent stimulus, which was designated as a “suppressive” effect.     

Iterative techniques for unbiased rating scales

Three iterative techniques for neutralizing the effects of stimulus bias in category rating experiments were examined with a wide variety of stimulus variables. Under all conditions examined, the iterative techniques quickly led to a stable category estimation. This result was obtained for stimulus variables with strong measurement properties, e.g. length and weight; for stimulus variables with only ordinal properties, e.g. emery papers; and for stimulus variables with only nominal properties, where an ordered set is obtained only in the course of the category scaling, e.g. female profiles.