Modification of the rat's acoustic startle response by antecedent visual stimulation.

Male hooded and albino rats were exposed to a light flash followed at various temporal intervals by a startle-eliciting 117 db. (re 20 muN/m2) burst of white noise. The visual stimulus engendered startle response inhibition (maximally when the lead time was 64-250 msec) as well as startle response latency reduction (maximally when the lead time was 2-8 msec). The temporal functions for the effects of visual stimuli paralleled those previously reported for startle modification by acoustic events. Further study revealed that, given optimal lead times, inhibition is produced reliably by weaker visual stimuli (3 X 10-6 cd-sec/cm2) than latency reduction (3 X 10-4 cd-sec/cm2). This differential sensitivity to visual stimuli is also analogous to previously reported findings for events in the acoustic environment. It reveals that the neural mechanisms that mediate latency reduction and inhibition can be engaged by either acoustic or visual stimulation.     

The effects of spatial frequency and temporal waveform on three measures of temporal processing

The effects of spatial frequency and temporal transition of sine-wave grating onset and offset were assessed using measures of reaction time, visual persistence, and temporal order judgements. The stimuli were lateralized fields, separated by 1 degree of visual angle. Slow temporal transition resulted in significantly poorer performance than did abrupt onset and offset, but spatial frequency had a minimal effect. Thus, the latency, temporal resolution, and temporal ordering of events are mediated by a mechanism that is sensitive to abrupt temporal transients. The stimulus conditions employed did not result in a shift in the point of subjective simultaneity.     

The Effects of Spatial Frequency and Temporal Waveform on Three Measures of Temporal Processing

The effects of spatial frequency and temporal transition of sine-wave grating onset and offset were assessed using measures of reaction time, visual persistence, and temporal order judgments. The stimuli were lateralized fields, separated by 1° of visual angle. Slow temporal transition resulted in significantly poorer performance than did abrupt onset and offset, but spatial frequency had a minimal effect. Thus, the latency, temporal resolution, and temporal ordering of events are mediated by a mechanism that is sensitive to abrupt temporal transients. The stimulus conditions employed did not result in a shift in the point of subjective simultaneity.     

Sensorimotor synchronization: Motor responses to pseudoregular auditory patterns

Musically trained and untrained subjects (N=30) were asked to synchronize their finger tapping with stimuli in auditory patterns. Each pattern comprised six successive tonal stimuli of the same duration, the first of which was accented by a different frequency. The duration of interstimulus onset intervals (ISIs) gradually increased or decreased in constant steps toward the end of the patterns. Four values of such steps were used in different trials: 20, 30, 45, and 60 msec. Various time-control mechanisms are hypothesized as being simultaneously responsible for subjects’ incorrect reproduction of the internal temporal ratios of the stimulus patterns. The mechanism of assimilation (of a central tendency) led subjects to enforce a regular (isochronous) structure on the patterns. The influence of other time-control mechanisms (distinction, subjective expression of an accent, sequential transfer) was expressed mainly in differences between intertap onset intervals (ITIs) and the corresponding ISIs at the beginning of the patterns. The duration of the first two ITIs was in the majority of the trials in an inverse ratio to the ratio of the respective ISIs. The distortions resulting from the timing mechanisms concerned were more pronounced in the performance of nonmusicians than in that of musicians.     

A constant error in the perception of brief temporal intervals

Ss were presented two stimuli of equal duration separated in time. The parrs of stimuli were vibrotactile, auditory, or visual. The Ss adjusted the time between the two stimuli to be equal to the duration of the first stimulus. The results show that for stimulus durations ranging from 100 to 1,200 msec, Ss set the tune between the two stimuli too long and by a constant amount. For vibrotactfle stimuli, the constant was 596 msec; for auditory stimuli, 657 msec; and for visual stimuli, 436 msec. Changing the intensity of the vibrotactile stimuli did not change the size of the constant error. When Ss were presented two tones with a burst of white noise between the tones and adjusted the duration of the white noise to be equal to the duration of the first tone, the white noise was not adjusted too long by a constant amount. The results suggest that there is a constant error in the perception of unfilled relative to filled temporal intervals.     

Visual onset expands subjective time

We report a distortion of subjective time perception in which the duration of a first interval is perceived to be longer than the succeeding interval of the same duration. The amount of time expansion depends on the onset type defining the first interval. When a stimulus appears abruptly, its duration is perceived to be longer than when it appears following a stationary array. The difference in the processing time for the stimulus onset and motion onset, measured as reaction times, agrees with the difference in time expansion. Our results suggest that initial transient responses for a visual onset serve as a temporal marker for time estimation, and a systematic change in the processing time for onsets affects perceived time.     

The effects of onset and offset warning and post-target stimuli on the saccade latency of children and adults

Two studies, involving children (mean age = 10 years) and adults, investigated the effects of visual stimulus onsets and offsets on the latency of saccades to peripheral targets. Saccade latency was reduced when foveal stimulus onsets or offsets preceded the target. When stimulus onset occurred 100 msec after target onset, the stimulus interfered with responding, with this interference effect significantly greater for children than for adults. When stimuli were presented in the peripheral visual field facilitation and interference effects were similar for children and adults. These results were interpreted as indicating that oculomotor processes are similar in children and adults while the stimulus intake processes that follow stimulus onset at the point of fixation have a greater interference effect on children's than on adults' eye movements.     

Judgments of synchrony between auditory and moving or still visual stimuli.

The flash-lag effect is a visual illusion wherein intermittently flashed, stationary stimuli seem to trail after a moving visual stimulus despite being flashed synchronously. We tested hypotheses that the flash-lag effect is due to spatial extrapolation, shortened perceptual lags, or accelerated acquisition of moving stimuli, all of which call for an earlier awareness of moving visual stimuli over stationary ones. Participants judged synchrony of a click either to a stationary flash of light or to a series of adjacent flashes that seemingly bounced off or bumped into the edge of the visual display. To be judged synchronous with a stationary flash, audio clicks had to be presented earlier--not later--than clicks that went with events, like a simulated bounce (Experiment 1) or crash (Experiments 2-4), of a moving visual target. Click synchrony to the initial appearance of a moving stimulus was no different than to a flash, but clicks had to be delayed by 30-40 ms to seem synchronous with the final (crash) positions (Experiment 2). The temporal difference was constant over a wide range of motion velocity (Experiment 3). Interrupting the apparent motion by omitting two illumination positions before the last one did not alter subjective synchrony, nor did their occlusion, so the shift in subjective synchrony seems not to be due to brightness contrast (Experiment 4). Click synchrony to the offset of a long duration stationary illumination was also delayed relative to its onset (Experiment 5). Visual stimuli in motion enter awareness no sooner than do stationary flashes, so motion extrapolation, latency difference, and motion acceleration cannot explain the flash-lag effect.     

Tactile perception of sequentially presented spatial patterns

Tactile pattern recognition was studied by presenting pairs of alphabetic shapes in rapid succession at the same anatomical location, the subject being required on each trial to identify bath of the patterns. Experimental variables were the duration of each stimulus and the time between stimuli. Three aspects of the observed interaction were (1) an increase in letter reversals for very short interstimulus intervals; (2) a greater percentage of first-response errors for short-stimulus onset intervals and a greater percentage of second-response errors for long-stimulus onset intervals; and (3) a crossover in the first- and second-response error rates in the range of 100 to 200 msec. after the onset of the first stimulus. These results are consistent with some of the temporal properties of models proposed for analogous visual tasks.     

Control of fixation duration in visual search and memory search: another look

In visual search a variable delay (up to 150 msec) between the beginning of each fixation and the onset of a search stimulus reduces the time (oculomotor latency) between stimulus onset and the subject's next saccadic eye movement. Two hypotheses for this effect of stimulus onset delay (SOD) were compared: first, process monitoring, that SOD simply serves as a warning interval to facilitate saccadic responses; and second, preprogramming, that saccades are preprogrammed at short SODs. In the first experiment SOD produced a decline in oculomotor latency in search similar to that seen in previous studies. In the second and third experiments, the size of the memory set in a Sternberg memory search paradigm was varied, or a mask flanking some of the search stimuli was used, to vary the processing time of each stimulus. Partial preprogramming of saccades at short delays would predict that increasing the processing time of individual stimuli would increase oculomotor latency at only short SODs. However, oculomotor latency increased equally at all SODs. In this search task, then, the SODs appeared to facilitate saccade initiation.     

The role of selective attention in visual awareness of stimulus features: Electrophysiological studies

Attention and awareness are closely related, but the nature of their relationship is unclear. The present study explores the timing and temporal evolution of their interaction with event-related potentials. The participants attended to specific conjunctions of spatial frequency and orientation in masked (unaware) and unmasked (aware) visual stimuli. A correlate of awareness appeared 100-200 msec from stimulus onset similarly to both attended and unattended features. Selection negativity (SN), a correlate of attentional selection, emerged in response to both masked and unmasked stimuli after 200 msec. This double dissociation between correlates of awareness and SN suggests that the electrophysiological processes associated with feature-based attentional selection and visual awareness of features can be dissociated from each other at early stages of processing. In a passive task, requiring no attention to the stimuli, early electrophysiological responses (before 200 msec) related to awareness were attenuated, suggesting that focal attention modulates visual awareness earlier than does selective feature-based attention.     

Visual perseveration in normal and mentally retarded children

Visual perseveration was investigated within mentally retarded and second, fifth, and eighth grade normal children (Ns = 12 each group). Subjects matched an auditorially presented click to the onset and offset of visually presented stimuli. Time differences between visual stimulus offset and the point at which subjects reported simultaneity of the click and visual stimulus offset was assumed to reflect visual perseveration. Results showed: (a) no differences between the normal children as a function of age; (b) no difference between groups for stimuli of 100 msec. or longer duration; and (c) retarded subjects judged stimuli of 20 and 50 msec. to be of shorter duration than did normal subjects. This highly specific distinction between retarded and normal subjects suggests a difference in an early stage of perceptual processing.     

The time course of response inhibition in masked priming

In two experiments, we studied the temporal dynamics of the response time effects of masked visual prime stimuli, as a function of stimulus eccentricity and size. Experiment 1 factorially varied prime-target congruency, eccentricity, and mask-target stimulus onset asynchrony. Early facilitative and late inhibitory effects of congruency were observed at all eccentricities, with temporal dynamics modulated by eccentricity. To test whether this dependence on eccentricity is due to cortical magnification, Experiment 2 varied stimulus size as well. Response inhibition time courses were influenced by size and eccentricity jointly, with no discernible difference when stimuli were matched for cortical magnification. Analysis of the individual time course data revealed that the timescale of inhibition changes with the strength of the cortical representation of the prime stimulus. This imposes constraints on possible models.     

Contribution of the dorsal subiculum to memory for temporal order and novelty detection using objects,odors, or spatial locations in the rat

The contribution of the dorsal subiculum (DS) to memory for temporal order and novelty detection was assessed using a spontaneous exploration paradigm with objects (visual/tactile stimuli), odors, or spatial locations (Hunsaker, Fieldsted, Rosenberg, & Kesner, 2008). Rats with selective excitotoxic lesions of the DS were compared to sham-operated rats (SHAM) in the two exploration tests. In temporal order tests, two previously explored stimuli were presented and normal rats typically show a preference for exploring the stimulus that was first explored compared to the other stimulus. In novelty detection tests, a familiar and a new stimulus were presented and normal rats typically have a preference for exploring new stimuli. In temporal order tests, results indicated that Group SHAM explored significantly more the first than the last stimulus they met when the stimuli were odors or objects. In addition, SHAM rats predictably displayed a significant preference for the new stimulus in the novelty detection tests with objects, odors, and spatial locations. Group DS did not differ from controls on the temporal order and the novelty detection tests with objects or odors. However, on the novelty detection test with spatial locations, Group DS differed from Group SHAM. These results suggest that the DS is necessary for the memory of spatial locations but not of objects and odors.     

Subjective shortening with filled and unfilled auditory and visual intervals in humans?

Two experiments tested humans on a memory for duration task based on the method of Wearden and Ferrara (1993), which had previously provided evidence for subjective shortening in memory for stimulus duration. Auditory stimuli were tones (filled) or click-defined intervals (unfilled). Filled visual stimuli were either squares or lines, with the unfilled interval being the time between two line presentations. In Experiment 1, good evidence for subjective shortening was found when filled and unfilled visual stimuli, or filled auditory stimuli, were used, but evidence for subjective shortening with unfilled auditory stimuli was more ambiguous. Experiment 2 used a simplified variant of the Wearden and Ferrara task, and evidence for subjective shortening was obtained from all four stimulus types.     

Effect of stimulus duration on perceptual onset and offset latencies

The effects of stimulus duration on perceptual onset and offset latency were compared in vision and audition. It was found that perceptual onset latency was independent of stimulus duration but that the perceptual offset latency was longer for brief stimuli than for stimuli that exceeded a critical duration. For stimuli longer than the critical duration, the perceptual onset and offset latencies were equal: The same temporal relationships were found in both modalities. The results indicate that for any specific stimulus parameters, reduction of stimulus duration results, ultimately, in a perception of fixed duration.     

判断框架对时序知觉位置启动效应的影响

研究采用包含两种判断框架（判断刺激出现的先后次序）的时序判断任务探讨了决策偏向对时序知觉位置启动效应的影响。实验结果表明,时序知觉中存在着位置启动效应,而且在两个靶刺激出现时间间隔不同时,被试在“哪个靶刺激先出现”和“哪个靶刺激后出现”两种判断框架下的正确率存在显著差异,但在两个靶刺激同时出现时并没有出现显著的判断框架效应。因此,本研究推测时序知觉位置启动效应的作用机制不仅包括知觉增强加工过程,而且也与认知决策有关,这为反应偏向理论提供了新的支持证据。     

Using computer‐assisted instruction to increase the eye gaze of children with autism

Many children diagnosed with autism spectrum disorders have difficulty making appropriate eye contact and engaging in joint attention. The current study evaluated a computer‐assisted instruction package (pairing visual stimuli with vocal stimuli) as a novel treatment to improve the eye gaze accuracy in 3 elementary school children with autism. The researchers measured the latency from a recorded verbal stimulus to the students making eye contact with pictures of familiar individuals displayed on a computer screen, and the duration for which eye gaze on the stimulus was maintained. An automated infrared camera system for measuring eye gaze was utilized that eliminated the need for an instructor to make subjective judgments regarding participants' eye gaze. For all three participants, duration of eye contact increased, and latency to responding decreased following exposure to the computer‐assisted instruction. The implications of these findings for the treatment of individuals with autism are discussed, along with suggestions for future research on the topic.     

Stroboscope motion: Effects of duration and interval1

The quality of stroboscope motion induced by the successive presentation of two illuminated squares obeys two rules. For all stimulus durations shorter than 100 msec, optimal motion occurs when the stimulus onsets differ by about 120 msec. For stimulus durations longer than 100 msec, optimal motion occurs when the second stimulus begins at the termination of the first stimulus. The two rules relating quality of motion to duration suggest a single principle, namely, that the quality depends only on the interval between the visual responses to the two stimuli. The interresponse interval at which motion is optimal is independent of stimulus duration.     

女性对新异性事件加工的偏向:来自ERP的证据

采用修订后的oddball范式,结合ERP技术考察女性与男性在加工中性新异刺激时的差异。ERP结果表明,在早期已经出现新异性效应。在300-500ms内,新异刺激在男性和女性被试中都比标准刺激诱发了更大的LPC。在500-700ms内,新异刺激仅在女性被试中比标准刺激诱发更大的LPC,在男性被试中没有显著差异。这些结果表明男性和女性都对中性新异刺激表现出加工偏向,但是女性对其加工的时间比男性更长。这可能与女性容易对显著性(salient)的刺激进行沉思(rumination)相关。