Are Visual Peripheries Forever Young?

Effectively managing visual search tasks across multiple spatial regions during daily activities such as driving, cycling, and navigating complex environments often overwhelms visual processing capacity, increasing the risk of errors and missed critical information. This study investigates an integrated approach that combines an Ambient Display system utilizing peripheral vision cues with traditional Head-Mounted Displays (HMDs) to enhance spatial search efficiency while minimizing cognitive burden. We systematically evaluated this integrated HMD-Ambient Display system against standalone HMD configurations through comprehensive user studies involving target search scenarios across multiple spatial regions. Our findings demonstrate that the combined approach significantly improves user performance by establishing a complementary visual system where peripheral stimuli effectively capture initial attention while central HMD cues provide precise directional guidance. The integrated system showed substantial improvements in reaction time for rear visual region searches and higher user preference ratings compared with HMD-only conditions. This integrated approach represents an innovative solution that efficiently utilizes dual visual channels, reducing cognitive load while enhancing search efficiency across distributed spatial areas. Our contributions provide valuable design guidelines for developing assistive technologies that improve performance in multi-region visual search tasks by strategically leveraging the complementary strengths of peripheral and central visual processing mechanisms.

To determine the diagnostic yield of the nerve-muscle-skin (NMS) biopsy in paediatric neurology practice. A consecutive series of 98 paediatric NMS biopsies done 1989-1994 retrospectively reviewed in the context of pre-biopsy clinical and laboratory parameters. Bivariate associations based on chi-square test. Unconfounded associations between pre-biopsy variables and positive diagnostic yield (PDY) assessed by multiple logistic regression. Fifty seven out of 98 patients central (global delay, seizures, abnormal CNS imaging) process; 41/98 patients peripheral (motor delay, weakness) process, electromyography-nerve conduction studies (EMG-NCS) 87/98 cases; abnormal 43/87. Positive diagnostic yield (PDY) in 42/98 (43%) biopsies. Statistically significant bivariate associations between PDY and pre-biopsy; age, presenting symptom, developmental delay, weakness, reflexes, CPK, lactate, EMG-NCS and process. Unconfounded associations demonstrated with PDY and age, reflexes and process. The presence of a peripheral process or an abnormal EMG-NCS strongly predictive of PDY: 34/41 (83%) peripheral process cases had PDY, 32/40 (80%) abnormal EMG-NCS cases had PDY, and 29/31 (93.5%) peripheral process and abnormal EMG-NCS cases had PDY. Abnormal EMG-NCS with central process improved PDY to 3/9 (33%) from 4/37 (11%) for normal EMG-NCS. NMS biopsy is a valuable diagnostic tool, particularly in the context of a suspected peripheral process or a central processes with an abnormal EMG-NCS.

The contribution of peripheral and central vision in the control of movement amplitude

The purpose of this study was to investigate the role of central and peripheral vision in expert decision making. A gaze-contingent display was used to selectively present information to the central and peripheral areas of the visual field while participants performed a decision-making task. Eleven skilled and eleven less-skilled male basketball players watched video clips of basketball scenarios in three different viewing conditions: full-image control, moving window (central vision only), and moving mask (peripheral vision only). At the conclusion of each clip participants were required to decide whether it was more appropriate for the ball-carrier to pass the ball or to drive to the basket. The skilled players showed significantly higher response accuracy and faster response times compared with their lesser-skilled counterparts in all three viewing conditions, demonstrating superiority in information extraction that held irrespective of whether they were using central or peripheral vision. The gaze behaviour of the skilled players was less influenced by the gaze-contingent manipulations, suggesting they were better able to use the remaining information to sustain their normal gaze behaviour. The superior capacity of experts to interpret dynamic visual information is evident regardless of whether the visual information is presented across the whole visual field or selectively to either central or peripheral vision alone.

It has been known for some time that visual information plays an important role in how we perceive speech. The present research examines how this visual information is processed in central and peripheral vision. The perception of visual images is carried out in the nervous system by a set of spatial frequency-tuned channels and the sensitivity to spatial resolution varies across the retina. The experiment was conducted using a gaze-contingent display system that records a person’s eye position and then displays different information to their peripheral and central vision. The amount of high spatial frequency information presented in the central and peripheral visual fields was manipulated and the effect on both audiovisual speech perception and natural gaze patterns was measured. Preliminary results show that when peripheral information is no longer adequate, gaze patterns become altered to gather important visual information. This suggests that information across the whole visual field influences audiovisual speech behavior.

1 The Relevance of Psychophysics for Speech Perception.- The role of psychophysics in understanding speech perception.- Central and peripheral processes in the perception of speech and nonspeech sounds.- Psychophysics versus specialized processes in speech perception: an alternative perspective.- Speech perception and the role of long-term memory.- Levels of representation of phonemes and bandwidth of spectral-temporal integration.- General discussion of session 1.- 2 Separation of Acoustic Events.- The meaning of duplex perception: sounds as transparant objects.- Perceptual separation of speech from concurrent sounds.- Sound separation and auditory perceptual organization.- On the significance of spectral synchrony for signal detection.- Auditory enhancement in speech perception.- General discussion of session 2.- 3 Dynamic Aspects.- Trading relations, acoustic cue integration, and context effects in speech perception.- Perceptual integration of rise time and silence in affricate/fricative and pluck/bow continua.- Reversal of the rise-time cue in the affricate/fricative contrast: an experiment on the silence of sound.- Possible acoustic bases for the perception of voicing contrasts.- Is there a natural sensitivity at 20ms in relative tone-onset-time continua? A reanalysis of Hirsh's (1959) data.- Auditory constraints on speech perception.- Studies of possible psychoacoustic factors underlying speech perception.- Perception of tone, band, and formant sweeps.- Psychophysical representation of stop consonant and temporal masking in speech.- Effects of stimulus dynamics on frequency discrimination.- Extending the search for a psychophysical basis for dynamic phonetic patterns.- General discussion of session 3.- 4 Timbre (Peripheral Constraints and Central Processes in the Perception of Complex Signals)..- Psychophysics of audio signal processing and the role of pitch in speech..- Does the human auditory system include large scale spectral integration?.- Some aspects of the sound of speech sounds.- Involvement of the critical band in identification, perceived distance, and discrimination of vowels.- Profile analysis and speech perception.- General discussion of session 4.- 5 Physiological Correlates of Speech Perception.- Peripheral auditory processing of speech information: implications from a physiological study of intensity discrimination.- Organization of the cochlear nucleus for information processing.- Changes in the phonemic quality and neural representation of a vowel by alteration of the relative phase of harmonics near F1.- Phase vowels.- Nonlinear responses, in the auditory nerve to vowel-related complex stimuli.- Discussion of physiological correlates of speech perception.- General discussion of session 5.- 6 Primary Speech Percepts.- English and French speech processing: some psycholinguistic investigations.- Units of organization and analysis in the perception of speech.- Implications from infant speech studies on the unit of perception.- General discussion of session 6.- 7 Psychophysics and Speech Perception in the Hearing-Impaired.- Relationship between psychophysical abilities and speech perception for subjects with unilateral and bilateral cochlear hearing impairments.- Speech-reception threshold in a fluctuating background sound and its possible relation to temporal auditory resolution.- Differences in listening strategies between normal and hearing-impaired listeners.- Critical bands in the perception of speech signals by normal and sensorineural hearing loss listeners.- Phase and the hearing-impaired.

Visual search has traditionally been studied in cognitive and perceptual paradigms, but little is known about how it contributes to visuomotor performance. We have developed a novel computational model to examine how three underlying processes of visual search (spatial planning, working memory, and peripheral visual processing) contribute to visual search during a visuomotor task. We show that deficits integrating spatial planning and working memory underlie abnormal performance in stroke survivors with frontoparietal damage.

So far, action recognition has been mainly examined with small point-light human stimuli presented alone within a narrow central area of the observer’s visual field. Yet, we need to recognize the actions of life-size humans viewed alone or surrounded by bystanders, whether they are seen in central or peripheral vision. Here, we examined the mechanisms in central vision and far periphery (40° eccentricity) involved in the recognition of the actions of a life-size actor (target) and their sensitivity to the presence of a crowd surrounding the target. In Experiment 1, we used an action adaptation paradigm to probe whether static or idly moving crowds might interfere with the recognition of a target’s action (hug or clap). We found that this type of crowds whose movements were dissimilar to the target action hardly affected action recognition in central and peripheral vision. In Experiment 2, we examined whether crowd actions that were more similar to the target actions affected action recognition. Indeed, the presence of that crowd diminished adaptation aftereffects in central vision as wells as in the periphery. We replicated Experiment 2 using a recognition task instead of an adaptation paradigm. With this task, we found evidence of decreased action recognition accuracy, but this was significant in peripheral vision only. Our results suggest that the presence of a crowd carrying out actions similar to that of the target affects its recognition. We outline how these results can be understood in terms of high-level crowding effects that operate on action-sensitive perceptual channels.

Vision Disorders and Visual Impairment

Information processing in the sensory periphery is shaped by natural stimulus statistics. In the periphery, a transmission bottleneck constrains performance; thus efficient coding implies that natural signal components with a predictably wider range should be compressed. In a different regime--when sampling limitations constrain performance--efficient coding implies that more resources should be allocated to informative features that are more variable. We propose that this regime is relevant for sensory cortex when it extracts complex features from limited numbers of sensory samples. To test this prediction, we use central visual processing as a model: we show that visual sensitivity for local multi-point spatial correlations, described by dozens of independently-measured parameters, can be quantitatively predicted from the structure of natural images. This suggests that efficient coding applies centrally, where it extends to higher-order sensory features and operates in a regime in which sensitivity increases with feature variability.

Information processing in the sensory periphery is shaped by natural stimulus statistics. In the periphery, a transmission bottleneck constrains performance; thus efficient coding implies that natural signal components with a predictably wider range should be compressed. In a different regime—when sampling limitations constrain performance—efficient coding implies that more resources should be allocated to informative features that are more variable. We propose that this regime is relevant for sensory cortex when it extracts complex features from limited numbers of sensory samples. To test this prediction, we use central visual processing as a model: we show that visual sensitivity for local multi-point spatial correlations, described by dozens of independently-measured parameters, can be quantitatively predicted from the structure of natural images. This suggests that efficient coding applies centrally, where it extends to higher-order sensory features and operates in a regime in which sensitivity increases with feature variability.DOI:http://dx.doi.org/10.7554/eLife.03722.001

Following auditory deprivation, the remaining sense of vision has shown selective enhancement in visual cognition, especially in the area of near peripheral vision. Visual acuity is poor in the far periphery and may be an area where sound confers the greatest advantage in hearing persons. Experience with a visuospatial language such as British Sign Language (BSL) makes additional demands on the visual system. To test the different and separable effects of deafness and use of a visuo-spatial language on far peripheral visual processing, we investigated visual reaction times (RTs) and response accuracy to visual stimuli, between 30° and 85° along the four cardinal and four inter-cardinal meridians. We used three luminances of static, briefly illuminated stimuli in visually normal adults. The cohort tested included profoundly congenitally deaf adults (N = 17), hearing fluent BSL users (N = 8) and hearing non-signing adults (N = 18). All participants were tested using a peripheral forced choice paradigm designed previously to test deaf and hearing children (Codina et al., 2011a). Deaf adults demonstrated significantly faster RTs to all far peripheral stimuli and exceeded the abilities of both signing and non-signing hearing adults. Deaf adults were significantly faster than BSL interpreters, who in turn were significantly faster than hearing non-signing adults. The differences in RT demonstrated between groups were consistent across all visual field meridians and were not localized to any one region of the visual field. There were no differences found between any groups in accuracy of detecting these static stimuli at any retinal location. Early onset auditory deprivation appears to lead to a response time visual advantage in far peripheral responses to briefly presented, static LED stimuli, especially in the right visual field. Fluency in BSL facilitates faster visuo-motor responses in the peripheral visual field, but to a lesser extent than congenital, profound deafness.

Using identical stimuli and methods, we assessed the effects of flankers on three different tasks, orientation discrimination, contrast discrimination, and detection, in central, peripheral, and amblyopic vision. The goal was to understand the factors that limit performance of a task in the presence of flankers in each of these visual systems. The results demonstrate that: (1) For unflanked targets, the losses in peripheral and amblyopic vision (relative to the normal fovea) are ordered, with the loss of unflanked contrast discrimination thresholds considerably smaller than those for either detection or orientation discrimination. (2) For flanked targets, in normal foveal vision and anisometropic amblyopia, the critical distance is more or less proportional to the target size, whereas in peripheral and strabismic amblyopic vision, the critical distance shows much less (or no) dependence on target size. (3) For the normal fovea, and anisometropic amblyopia, when the target is large (>≈0.2 deg) the amount of threshold elevation induced by flankers is low, increasing when the target is very small. On the other hand, for the periphery and the amblyopic eyes of most strabismic amblyopes, the elevation is large over the range of sizes tested. (4) In peripheral and strabismic amblyopic vision, remote flankers elevate orientation discrimination and contrast discrimination thresholds but not detection thresholds. Our results show clearly that the effects of flanks depend on both the task and the type of visual system. We conclude that in normal foveal vision and anisometropic amblyopia, the effects of flankers largely reflects a reduction in visibility and may be explained by masking. On the other hand, in peripheral vision and strabismic amblyopia, the effects of flankers on orientation discrimination and to a lesser extent contrast discrimination cannot be explained by simple masking and are due to crowding.

Peak latency of the inferior collicular response (wave V) of the brainstem auditory evoked potential (BAEP) increases with decreasing interstimulus interval (ISI). The present research investigated relative peak shifts of major components of the BAEP in an attempt to identify the source of the observed shift in wave V. Peripheral as well as central transmission times (CTT) were computed for 9 young adults between an ISI of 100 msec and an ISI of 10 msec. The results indicate that shifts in wave V latency with changing ISI are due to a combination of central and peripheral processes. The magnitude of the shift observed for wave V was approximately 0.50 msec. This increase in latency was accounted for by an average 0.29 msec increase in peripheral transmission time, a 0.14 msec increase in CTT between waves I and III, and a 0.07 msec increase in CTT between waves III and V. The results suggest a dual process underlying latency changes in wave V of the BAEP as a function of decreasing ISI. These are peripheral adaptation or fatigue and central processes that may include short-term habituation.

Serotoninlike immunoreactivity was examined by the fluorescein-isothiocyanate-labeled secondary antibody technique in the lateral eye and brain of Limulus. Endogenous serotonin was measured with high-performance liquid chromatography and electrochemical detection. The synthesis of [3H]serotonin from [3H]tryptophan was measured in the presence and absence of reserpine. Fibers with serotoninlike immunoreactivity were found in the proximal stalks of the corpora pedunculata, in the neuropil of the central body, in the neuropils of the visual centers (lamina, medulla, and ocellar ganglion), in the optic tract that connects the ocellar ganglion with the posterior medial medulla, and in the central neuropil of the brain. Immunoreactive somata were found in four groups in the brain. Up to 50 somata were scattered through each side of the dorsal medial group that lies centered on the dorsal surface within the curve of the central body. These neurons innervate the central body neuropil and send processes into the central neuropil. Three or four reactive somata formed the ventral pole of each medullar group. These may provide the innervation of the proximal stalk of the corpora pedunculata. Five to ten reactive neurons were observed anteriorly in the ventral posterior lateral group #2 on each side that send processes into the central neuropil. Ten to 15 reactive somata were found on either side of the midline in the dorsal anterior part of the ventral medial group that contribute processes to the central neuropil. The remainder of the brain was not immunoreactive. No immunoreactive fibers or somata were found in the lateral eye or in the lateral optic nerve. Serotoninlike and substance P-like immunoreactivities were not found to be colocalized anywhere in the brain. Significant amounts of endogenous serotonin were detected in the lamina and medulla whose neuropils are rich in immunoreactive fibers and in the central body and dorsal medial group that are also rich in immunoreactive somata and fibers. No endogenous serotonin was detected in either the lateral eye or the lateral optic nerve. The lamina, medulla, and central body and dorsal medial group also synthesized and stored [3H]serotonin from [3H]tryptophan. It is likely that serotonin is a neurotransmitter in the brain, but not in the lateral eye of the horseshoe crab. In particular, it appears that serotoninergic neurons may play a role in central visual processing.