Electrocutaneous stimulation L The effects of stimulus parameters on absolute threshold

Thresholds for detecting electrical stimulation were measured as a function of (1) body locus, (2) electrode configuration, (3) stimulus waveform, and (4) pulse duration. The results were: (1) the forehead gave slightly, but not reliably, lower thresholds than the abdomen; (2) concentric electrodes gave slightly, but not reliably, lower thresholds than unifocal electrodes; (3) cathodal monophasic (?) pulses and biphasic pulses (+/? and ?/+) gave identical thresholds, while anodal monophasic (+) pulses gave higher thresholds; and (4) thresholds decreased as pulse duration increased up to .5 msec, but changed less with longer pulses.     

Interval patterning and auditory gap detection

Pattern effects associated with the perception of the temporal microstructure of auditory signals were examined. Temporal changes, or gaps, were introduced into auditory interval patterns produced by a sequence of pulses. Discrimination thresholds for positive, and for negative, gaps were obtained as a function of the surrounding pattern of intervals. Gap thresholds increase with the slope of the surrounding interval pattern. Gap thresholds are smaller when the gap interval represents an extension, rather than a reversal, of the surrounding pattern. The results are in agreement with Heise and Miller’s thresholds of tonal isolation from repeated melodies, and with Mangelsdorf’s visual extrapolation thresholds of point-of-collision. The agreement of results from diverse test situations suggests a non-specifiC., general patterning effect upon discontinuity thresholds.     

Sensitivity to shifts of a point stimulus: An instance of tactile hyperacuity

The sensitivity of the tactile sense to shifts in the position of a point stimulus was determined at four body loci: the index finger, forehead, belly, and back. Water-jet stimulation was used, a method which allows frictionless travel of a point stimulus over the skin. Three subjects were tested by means of the method of forced choice, with the task being to say whether the stimulus moved to the right or to the left. The shift threshold was defined as that shift excursion which gave rise to 75% correct responding. The basic finding was that shift thresholds were on the order of 10 to 30 times smaller than the corresponding two-point limens obtained by Weinstein (1968) for the same body loci. These unexpectedly small shift thresholds indicate an exquisite sensitivity of the cutaneous sense to rapid changes in position of a point stimulus. A physiological model is presented which accounts for the difference between localization and spatial resolution. nt]mis|This research was supported by Department of Health~ Education, and Welfare Grant 14-P-SS282/9 from the Social and Rehabilitation Services, NIH Research Grant R01-EY-00686 from the National Eye Institute, and the Smith-Kettlewell Eye Research Foundation.     

Memory processing of spatial order as transmitted by auditory information in the absence of visual cues

Two experiments were conducted concerning spatial order recall when spatial information is transmitted by auditory stimuli. Temporal order either was congruent with spatial order or was independent of spatial order. In Experiment 1, the comparisons were among normally or partially sighted subjects allowed to look, normally sighted subjects who were blindfolded, and blind children. The main findings were a superiority of the sighted subjects allowed to look (that is, to support auditory information with visual cues) and a smaller advantage for the sighted-but-blindfolded subjects, relative to the blind group. In Experiment 2, normally sighted adults (either seeing or blindfolded) and blind adults were tested. Surprisingly, the blind were not worse than the sighted in this study. Subsequent interviews and detailed analysis of errors suggested that the blind coded spatial information kinesthetically. These indirect analyses also suggested that whereas spatial order was coded temporally in the sighted, it was controlled by both temporal and spatial factors in the blind and blindfolded subjects.     

Effects of sleep deprivation on performance and EEG spectral analysis in young adults

Nine totally sleep deprived (TSD) and nine control subjects were evaluated with a complete battery for attention and memory performance. Frontal and temporal EEGs (5 min, eyes closed) were also recorded before and after the night. TSD subjects exhibited three performance deficits: learning the Pursuit Rotor Task, implicit recall of paired words, and distractibility on the Brown-Peterson Test. Relative to evening recordings, control subjects showed decreased morning absolute powers in all electrodes for all frequencies except for Frontal delta; TSD subjects showed increased Frontal and Temporal theta and Frontal beta. These results show that motor procedural, implicit memory, and working memory are sensitive to one night of TSD, and that Frontal and Temporal theta spectral power seem to discriminate between a night with sleep from a night without.     

The T?lz Temporal Topography Study: Mapping the visual field across the life span. Part I: The topography of light detection and temporal-information processing

Temporal performance parameters vary across the visual field. Their topographical distributions relative to each other and relative to basic visual performance measures and their relative change over the life span are unknown. Our goal was to characterize the topography and age-related change of temporal performance. We acquired visual field maps in 95 healthy participants (age: 10?C90?years): perimetric thresholds, double-pulse resolution (DPR), reaction times (RTs), and letter contrast thresholds. DPR and perimetric thresholds increased with eccentricity and age; the periphery showed a more pronounced age-related increase than the center. RT increased only slightly and uniformly with eccentricity. It remained almost constant up to the age of 60, a marked change occurring only above 80. Overall, age was a poor predictor of functionality. Performance decline could be explained only in part by the aging of the retina and optic media. In Part II, we therefore examine higher visual and cognitive functions.     

Neural correlates of coherent and biological motion perception in autism

Recent evidence suggests those with autism may be generally impaired in visual motion perception. To examine this, we investigated both coherent and biological motion processing in adolescents with autism employing both psychophysical and fMRI methods. Those with autism performed as well as matched controls during coherent motion perception but had significantly higher thresholds for biological motion perception. The autism group showed reduced posterior Superior Temporal Sulcus (pSTS), parietal and frontal activity during a biological motion task while showing similar levels of activity in MT+/V5 during both coherent and biological motion trials. Activity in MT+/V5 was predictive of individual coherent motion thresholds in both groups. Activity in dorsolateral prefrontal cortex (DLPFC) and pSTS was predictive of biological motion thresholds in control participants but not in those with autism. Notably, however, activity in DLPFC was negatively related to autism symptom severity. These results suggest that impairments in higher-order social or attentional networks may underlie visual motion deficits observed in autism.     

Age-of-acquisition effects in novel picture naming: A laboratory analogue

Age-of-acquisition (AoA) effects are such that early-acquired items are more quickly recognized and produced than later acquired items. In this laboratory analogue, participants were trained to name a group of Greeble pictures with a novel nonsense name. We manipulated order of acquisition of the stimuli: Half of the stimuli were presented from the onset of training (early acquired) whilst the other half were introduced later in the training schedule (late acquired). At test, when early and late stimuli had equal cumulative frequency, early stimuli were named significantly faster than late items. In a second test, it was also found that visual duration thresholds were significantly smaller for the early items when participants were asked to name the critical items. These findings support the notion that order-of-acquisition effects can be manifest over a short time span in the laboratory, and that the effect of order of acquisition is distinct from mere frequency of exposure. The findings are consistent with the idea that AoA effects occurring over a large temporal scale may be a special case of more general order-of-acquisition effects, and both may be a general property of learning mechanisms.     

Grouping and short-term memory: Different means and patterns of grouping

Two experiments, concerned with the improving effects of grouping on auditory short-term memory, are described. In the first, temporal grouping was found to improve recall considerably, but non-temporal grouping had a much smaller effect. Temporal grouping reduced the order errors more than other errors; it also changed the pattern of the order errors. Further, it altered the shape of the serial position curve of all errors. In the second experiment, irregular patterns of temporal grouping were found to be inferior to a regular pattern. The results are discussed in terms of the time available for processing previous items during the presentation of a sequence, and the form that this processing may take.     

Frames of reference in preschoolers’ perception of motion

Experiments 1 and 2 established children’s (mean age 3 years, 7 months) subject-relative and object-relative motion thresholds at 1°31.37′/sec and 1°9.33′/sec, respectively, speeds well above those found for adults. Experiment 3 established that preschoolers, like adults, attribute object-relative motion to the smaller of two objects, with the inducing properties of the larger stimulus greatest when it is surrounding rather than adjacent to a smaller stimulus. The inducing advantage of surroundedness was equivalent for a single-element square frame and a multielement six-dot frame.     

Temporal order perception of auditory stimuli is selectively modified by tonal and non-tonal language environments

The close relationship between temporal perception and speech processing is well established. The present study focused on the specific question whether the speech environment could influence temporal order perception in subjects whose language backgrounds are distinctively different, i.e., Chinese (tonal language) vs. Polish (non-tonal language). Temporal order thresholds were measured for both monaurally presented clicks and binaurally presented tone pairs. Whereas the click experiment showed similar order thresholds for the two language groups, the experiment with tone pairs resulted in different observations: while Chinese demonstrated better performance in discriminating the temporal order of two “close frequency” tone pairs (600 Hz and 1200 Hz), Polish subjects showed a reversed pattern, i.e., better performance for “distant frequency” tone pairs (400 Hz and 3000 Hz). These results indicate on the one hand a common temporal mechanism for perceiving the order of two monaurally presented stimuli, and on the other hand neuronal plasticity for perceiving the order of frequency-related auditory stimuli. We conclude that the auditory brain is modified with respect to temporal processing by long-term exposure to a tonal or a non-tonal language. As a consequence of such an exposure different cognitive modes of operation (analytic vs. holistic) are selected: the analytic mode is adopted for “distant frequency” tone pairs in Chinese and for “close frequency” tone pairs in Polish subjects, whereas the holistic mode is selected for “close frequency” tone pairs in Chinese and for “distant frequency” tone pairs in Polish subjects, reflecting a double dissociation of function.     

触觉时序知觉手臂交叉效应的性别差异

本研究探讨触觉时序知觉的手臂交叉效应是否存在性别差异。通过两个实验在较短和较长的SOA条件下考察男性和女性被试在基于体觉和基于外部空间的触觉时序判断任务中的表现。结果表明,男性与女性被试在基于体觉和基于外部空间的触觉时序判断任务中均存在手臂交叉效应,SOA较短时男性被试的手臂交叉效应显著小于女性被试,但在SOA较长的条件下手臂交叉效应没有明显的性别差异。触觉时序知觉手臂交叉效应的性别差异可能与空间知觉能力和生理解剖学因素有关。     

Effect of masker level on infants’ detection of tones in noise

In adult listeners, the signal-to-noise ratio at masked threshold remains constant with increases in masker level over a wide range of stimulus conditions. This relationship was examined in 7-month-old infants by obtaining masked thresholds for .5- and 4-kHz tones presented in four levels of continuous masking noise. Adults were also tested for comparison. Masker spectrum levels ranged from 5 to 35 dB/Hz for .5-kHz tones, and from ?5 to 25 dB/Hz for 4-kHz stimuli. Thresholds were determined for stimuli of both 10 and 100 msec in duration. The results indicated that infants’ performance was more adultlike for 4-kHz stimuli. Although mean thresholds for both 10- and 100-msec, 4-kHz tones were approximately 7 dB higher in infants than in adults, E/N₀ at threshold remained essentially constant over the 30-dB range of maskers employed. By contrast, infants’ thresholds for .5-kHz tones were exceptionally high at lower levels of the masker. Threshold E/N0 decreased significantly as masker level increased from 5 to 35 dB/Hz, and this decrease was significantly greater for 10- than for 100-msec stimuli. Temporal summation of .5-kHz tones, measured as the difference between thresholds obtained at the two signal durations, was greater for infants than for adults at low levels of the masker. However, because infants’ thresholds improved more rapidly with level for 10- than for 100-msec tones, age differences in temporal summation were no longer significant when masker spectrum level was 35 dB/Hz. These results suggest that the relationship between signal-to-noise ratio at masked threshold and level of the masker is dependent on both signal frequency and duration during infancy.     

Effect of masker level on infants' detection of tones in noise

In adult listeners, the signal-to-noise ratio at masked threshold remains constant with increases in masker level over a wide range of stimulus conditions. This relationship was examined in 7-month-old infants by obtaining masked thresholds for .5- and 4-kHz tones presented in four levels of continuous masking noise. Adults were also tested for comparison. Masker spectrum levels ranged from 5 to 35 dB/Hz for .5-kHz tones, and from -5 to 25 dB/Hz for 4-kHz stimuli. Thresholds were determined for stimuli of both 10 and 100 msec in duration. The results indicated that infants' performance was more adult-like for 4-kHz stimuli. Although mean thresholds for both 10- and 100-msec, 4-kHz tones were approximately 7 dB higher in infants than in adults, E/N0 at threshold remained essentially constant over the 30-dB range of maskers employed. By contrast, infants' thresholds for .5-kHz tones were exceptionally high at lower levels of the masker. Threshold E/N0 decreased significantly as masker level increased from 5 to 35 dB/Hz, and this decrease was significantly greater for 10- than for 100-msec stimuli. Temporal summation of .5-kHz tones, measured as the difference between thresholds obtained at the two signal durations, was greater for infants than for adults at low levels of the masker. However, because infants' thresholds improved more rapidly with level for 10- than for 100-msec tones, age differences in temporal summation were no longer significant when masker spectrum level was 35 dB/Hz. These results suggest that the relationship between signal-to-noise ratio at masked threshold and level of the masker is dependent on both signal frequency and duration during infancy.     

时序知觉研究方法及其影响因素

时序知觉是个体对直接作用于感觉器官的客观事件顺序性的知觉。时序判断任务和同时性判断任务是研究时序知觉的经典实验范式。时序知觉不仅受机体变量,刺激变量及反应变量的影响,还受注意和通道等中介变量的影响。个体的意识和潜意识在同时性、非同时性和序列性时间知觉中的作用问题有待进一步探索。     

The effect of marker frequency disparity on the discrimination of gap duration in monkeys

Duration-discrimination thresholds of the silent interval (gap) between two successive tones (markers) were measured in four Japanese monkeys. The task was serial discrimination, and monkeys were required to release the lever when the gap duration decreased from 200 ms. Monkeys successfully acquired the task, and gap thresholds of monkeys were revealed to be larger than previous data with human subjects. Gap thresholds were not affected by marker frequency when the two markers were identical in frequency, though the thresholds increased when large frequency differences existed between markers. The effect of marker frequency disparity on gap thresholds in monkeys is discussed in terms of the difficulty in integrating information from discrete frequency channels.     

Visual Search for a Tilted Target: Tests of Spatial Uncertainty Models

We report that spatial cueing of a parafoveal target in the presence of distractors enhances orientational acuity for that target. When no distractors were present, orientation thresholds were in the range 1-4 . For long exposure times, distractors increased threshold by the amount predicted from a winner-takes-all spatial uncertainty model. For short (100-msec) exposures followed by a random dot mask, the rise in threshold with distractors was considerably greater than that predicted from spatial uncertainty. For brief exposures the effect of distractors was greater when the target and distractors were spatially crowded rather than widely spaced. Adding a tilt to the distractors in the opposite direction to the target increased thresholds still further. Cueing the target with a spatial pointer decreased the effect of distractors, even when they were crowded. We suggest that when attention cannot be appropriately focused, discrimination is carried out by a relatively coarse texture analyser, which averages over several elements, and that focused attention permits the analysis of the target over a smaller area of space.     

The perception of pure and mistuned musical fifths and major thirds: Thresholds for discrimination,beats, and identification

In Experiment 1, the discriminability of pure and mistuned musical intervals consisting of simultaneously presented complex tones was investigated. Because of the interference of nearby harmonics, two features of beats were varied independently: (1) beat frequency, and (2) the depth of the level variation. Discrimination thresholds (DTs) were expressed as differences in level (AL) between the two tones. DTs were determined for musical fifths and major thirds, at tone durations of 250, 500, and 1,000 msec, and for beat frequencies within a range of .5 to 32 Hz. The results showed that DTs were higher (smaller values of ΔL) for major thirds than for fifths, were highest for the lowest beat frequencies, and decreased with increasing tone duration. Interaction of tone duration and beat frequency showed that DTs were higher for short tones than for sustained tones only when the mistuning was not too large. It was concluded that, at higher beat frequencies, DTs could be based more on the perception of interval width than on the perception of beats or roughness. Experiments 2 and 3 were designed to ascertain to what extent this was true. In Experiment 2, beat thresholds (BTs) for a large number of different beat frequencies were determined. In Experiment 3, DTs, BTs, and thresholds for the identification of the direction of mistuning (ITs) were determined. For mistuned fifths and major thirds, sensitivity to beats was about the same. ITs for fifths and major thirds were not significantly different; deviations from perfect at threshold ranged from about 20 to 30 cents. Comparison of the different thresholds revealed that DTs are mainly determined by sensitivity to beats. Detailed analysis, however, indicated that perception of interval width is a relevant aspect in discrimination, especially for the fifths.     

Differentiation of retinal and nonretinal contributions to averaged evoked responses obtained with electrodes placed near the eyes

Recent visual evoked potential (VEP) studies suggest that during sustained voluntary attention, irrelevant or unattended visual stimuli may be filtered precortically. Testing of this hypothesis in humans requires knowledge of the origin of specific components of the VEP that are affected by selective attention. This study describes techniques and procedures for distinguishing between retinal and nonretinal components of VEPs recorded from electrodes placed strategically around the eyes and on the forehead. By visually stimulating one eye at a time while recording simultaneously from both, and by stimulating a given retinal area with the eyes fixated on the target at different angular deviations from the normal line of regard, components of the VEPs around the eyes can be distinguished as of retinal or nonretinal origin. The results are discussed in terms of volume conduction theory.     

Aggressive behavior induced by electrical stimulation in the midbrain central gray of male rats

Electrical stimulation via electrodes implanted in the lateral hypothalamus may induce intraspecific aggressive behavior. Small electrolytic lesions placed via these electrodes resulted in a five– to tenfold increase in the current threshold for aggression. Degenerating fibers were stained by means of the Fink-Heimer method and could be followed caudally to the dorsal midbrain central gray and to the mammillary bodies. A few axons could be traced rostrally to the medial septum. Aggression could be induced from 10 of 112 electrodes implanted in the central gray; the other electrodes elicited either locomotion, vocalization, jump, or “alarm-like reactions.” The morphology of the induced aggression was similar to the morphology of the hypothalamically induced aggression, though it was often accompanied with motor disturbances and was less intense. Hypothalamic stimulation was combined with simultaneous central gray stimulation in rats with electrodes both in the hypothalamus and in the central gray. Hypothalamic thresholds for aggression could be lowered by this stimulation of the central gray, even when no aggressive responses were observed during central gray stimulation alone. This suggests that, although aggression is not manifest, electrical stimulation may activate neural tissue involved in aggressive behavior. It is concluded that in rats central gray and hypothalamus are part of the same neural network mediating intraspecific aggression.