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Responses of neurons in inferior colliculus to variations in sound-source azimuth.

This study aimed to classify the responses of single units in the auditory midbrain to acoustic stimuli presented in the free field in order to characterize those units likely to have a role in sound localization in the horizontal plane. The responses of 131 single units in the inferior colliculus of the cat and the brush-tailed possum were studied using tone and noise-burst stimuli presented from a speaker capable of movement at any point along a plane 10 degrees above the horizontal plane. Speaker positions along this plane are referred to as speaker azimuths; those on the same side as the recorded inferior colliculus as ipsilateral, and on the opposite side as contralateral, azimuths. For each unit, spike counts were measured as a function of azimuth either at the best frequency (BF) or using noise bursts. These functions are referred to as azimuth functions and were usually measured for at least two intensities, between 10 and 70 dB above threshold. The recording sites of most units were identified histologically with the aid of microlesions and were related to the major subdivisions of the inferior colliculus: the central nucleus (ICC), the lateral part of the external nucleus (ICX), and the rostroventral process (R-ICX). Two units were located in the pericentral nucleus and two in the dorsal nucleus of the lateral lemniscus. Two major classes of neuron were identified: omnidirectional and directionally sensitive. Omnidirectional units exhibited azimuth functions that were either flat or that declined gradually at progressively ipsilateral azimuths. For the latter units, discharge rates at all points monotonically increased with stimulus intensity. There was no indication, for either type of omnidirectional unit, of significant binaural interaction. A good correlation was found between the summed proportions of excitatory-excitatory (EE) and monaural (EO) units observed in dichotic studies (46-55%) and the proportion of omnidirectional units in the present study (47%). A subgroup of directionally sensitive units (36% of the total) displayed azimuth functions for which the azimuthal position of the discharge border or peak firing azimuth remained essentially unaltered over a range of stimulus intensities. These azimuth-selective units are likely to have a role in the detection of the location of stimuli in the horizontal plane and appear to include units that would be considered excitatory-inhibitory (EI) or delay sensitive in dichotic studies. The azimuths over which directionally sensitive units showed their marked directional effects were influenced by the position of the contralateral pinna.(ABSTRACT TRUNCATED AT 400 WORDS)

Animals↗

Modulation by a moving texture of cat area 18 neuron responses to moving bars.

1. The influence of a moving texture on neuronal responses to a moving bar was tested in 103 area 18 neurons of anesthetized and paralyzed cats. The texture was a two-dimensional noise pattern, the bar moved at optimal speed, and its contrast was adjusted to yield 50% of the maximum response. 2. The moving texture exerted two different but related effects: it suppressed the response of area 18 neurons to the moving bar, and it modulated the direction selectivity of parastriate neurons. These effects were strongest when the texture moved at the same speed or faster than the bar. 3. Genuine suppressive effects of the moving texture were distinguished from lack of summation between bar and texture responses. Suppressive effects of either type were observed in 75% of the area 18 cells and occurred more frequently among C family cells, velocity tuned cells, and in layer 5 than in other groups of cells. 4. The modulation of direction selectivity was distinguished from pseudomodulation because of lack of summation of bar and texture responses. The direction selectivity of 35% of the area 18 cells was modulated by the moving texture. Six different relative direction selectivity (RDS) types were observed in area 18. 5. The neurons of which direction selectivity was modulated by the moving texture occurred predominantly in layers 2-3 and 6, suggesting that they represent a further stage of processing within area 18. 6. Many (75%) area 18 cells responded to the texture moving on its own. Most of these cells respond to isolated features ("grains") in the patterns rather than to the movement of the whole pattern. Cells responding to the movement of the whole pattern were generally C family cells, and their direction selectivity was not modulated by the moving texture. 7. These results are compared with those obtained under identical experimental conditions in area 17. Although suppressive effects are similar in both areas, RDS types are differently distributed in the two areas. 8. The possible origins of the interactions and their functional significance are discussed.

Animals↗

Encoding of binocular disparity by complex cells in the cat's visual cortex.

To examine the roles that complex cells play in stereopsis, we have recorded extracellularly from isolated single neurons in the striate cortex of anesthetized paralyzed cats. We measured binocular responses of complex cells using a comprehensive stimulus set that encompasses all possible combinations of positions over the receptive fields for the two eyes. For a given position combination, stimulus contrast could be the same for the two eyes (2 bright or 2 dark bars) or opposite (1 bright and 1 dark). These measurements provide a binocular receptive field (RF) profile that completely characterizes complex cell responses in a joint domain of left and right stimulus positions. Complex cells typically exhibit a strong selectivity for binocular disparity, but are only broadly selective for stimulus position. For most cells, selectivity for disparity is more than twice as narrow as that for position. These characteristics are highly desirable if we assume that a disparity sensor should exhibit position invariance while encoding small changes in stimulus depth. Complex cells have nearly identical binocular RFs for bright and dark stimuli as long as the sign of stimulus contrast is the same for the two eyes. When stimulus contrast is opposite, the binocular RF also is inverted such that excitatory subregions become suppressive. We have developed a disparity energy model that accounts for the behavior of disparity-sensitive complex cells. This is a hierarchical model that incorporates specific constraints on the selection of simple cells from which a complex cell receives input. Experimental data are used to examine quantitatively predictions of the model. Responses of complex cells generally agree well with predictions of the disparity energy model. However, various types of deviations from the predictions also are found, including a highly elongated excitatory region beyond that supported by a single energy mechanism. Complex cells in the visual cortex appear to provide a next level of abstraction in encoding information for stereopsis based on the activity of a group of simple-type subunits. In addition to exhibiting narrow disparity tuning and position invariance, these cells seem to provide a partial solution to the stereo correspondence problem that arises in complex natural scenes. Based on their binocular response properties, these cells provide a substantial reduction in the complexity of the correspondence problem.

Animals↗

Glare disability and driving safety.

PURPOSE: Increasing investigation of the visual elements of safe driving environments may be of great benefit to society. Visual disability appears to be only one of many visual factors related to traffic accidents. The purpose of this article was to examine the type of visual impairment mediated by the increased glare sensitivity in adult drivers using the original halometer glare test. METHODS: In this article, the visual sensory, cognitive and motor functions relevant to driving, their measurement, the epidemiology and prevention of age-associated functional impairments and the relationship of functional impairments to both self-reported driving and the imposition of legal restrictions are reviewed. RESULTS: The problem of night and tunnel driving is the most urgent in relation to the effects of glare from vehicle headlights on motion perception of drivers. The reduced mesopic vision and increased sensitivity to glare are accompanied by an increased risk of nighttime accidents. Elderly drivers and patients with beginning cataract cannot sufficiently fulfill the criteria for night driving ability because of contrast and glare sensitivity. It is indispensable for the parameters mentioned to be carefully measured and for drivers to be informed that night driving ability may be impaired, even if visual acuity is sufficient. CONCLUSIONS: It would be advisable for traffic safety if simple tests for contrast and glare sensitivity were implemented for vehicles and/or were regularly added to the requirements for a driver's licence, at least for older drivers. The age, functional status and test result limits should be defined to avoid a risk factor in traffic.

Accidents, Traffic↗

Recognition of apertures in overhead transparent barriers by leopard frogs.

Anurans have independent systems for detecting moving stimuli and stationary opaque objects. We have discovered that leopard frogs will also orient to, and spontaneously and accurately jump through, circular apertures in overhead transparent covers. When given a choice between one large aperture of 3.8 cm diameter, and three apertures of smaller but equal diameter (2.5 cm diameter, 1.9 cm diameter, or 1.3 cm diameter) they choose the larger diameter aperture at a frequency (64, 87 and 97%, respectively) that is statistically greater than chance. In only 1 of 255 attempts was there a jump to the overhead cover that was not directed at an aperture. Atectal frogs are still able to detect and jump accurately through transparent apertures. Frogs cannot distinguish between two apertures of equal diameter if one aperture is covered with clear plastic with high light transmissibility (92% of transmissibility of air). However, if the plastic covering of the aperture has a residue which reduces light through the cover from 92 to 87% of the transmissibility of air, frogs will jump to the uncovered aperture at a frequency that is statistically greater than chance. Our results show that leopard frogs have an extremely well developed ability to detect overhead apertures just as they can vertical obstacles. They are able to jump towards such openings with a small margin of error independent of the tectal visual system.

Animals↗

Discrimination of visual stimuli representing prey versus non-prey by the praying mantis Sphodromantis lineola (Burr.).

Adult, female praying mantids, Sphodromantis lineola (Burr.), were presented with seventy, flat black rectangles which moved toward the mantids (in the horizontal plane) against a white background. The lengths of the lures' edges parallel to their direction of movement, 1(1), were 1.5, 3, 6, 12, 18, 24, 30, 54, 72, or 114 mm; the edge lengths perpendicular to movement direction, 1(2), were 1.5, 3, 6, 12, 18, 24, or 30 mm. Mantids emitted the most predatory behaviors to square lures (1[1] = 1[2]) for which 1(1, 2) = 3-12 mm, and to 'worm' lures (1[1] greater than 1[2]) for which 1(2) = 1.5-6 mm. 'Anti-worm' lures (1[1] less than 1[2]) were poor releasers of predatory behavior. These results reconcile seemingly discrepant findings between studies that have presented mantids with various types of oscillating, rotating and/or three-dimensional lures. Further, the results indicate that like other terrestrial predators, such as toads, prey recognition by S. lineola is approximate and based on the spatiotemporal relationships between the features of moving objects (i.e. worm versus anti-worm). These findings are congruent with data on mantid prey selection in the wild.

Animals↗

Central and peripheral visual interactions in disparity-induced vergence eye movements: I. Spatial interaction.

PURPOSE: To evaluate the interaction between central and peripheral disparities in the initiation of vergence eye movements. METHODS: Eye movements were recorded in eight normal subjects using an infrared limbus tracker. Three-dimensional visual stimuli were back projected onto a tangent screen by using two liquid crystal display (LCD) projectors through crossed polarizers. The central target was a vertical bar, which always jumped from 2 to 1 m. The peripheral target was a random-dot pattern that jumped from 2 to 0.75, 1, or 1.5 m (near planes), 2 m (no change), or 3 m (far plane) simultaneously with the central target jump. Latency, amplitude at 150 ms, and average amplitude over 1 to 2 seconds after vergence onset; peak velocity; and the main-sequence relationship of the initial vergence response were calculated. How far the central target appeared to jump was scored subjectively. RESULTS: In half of the subjects, there was a clear effect of the peripheral disparity on the dynamics of the vergence response to the central disparity. The amplitude of vergence at 150 ms, as an index of open-loop gain, was significantly greater when the peripheral target moved closer, but steady state amplitude (average during 1-2 seconds) did not change, and the vergence latency was significantly greater when the peripheral target jumped away. There was no obvious relationship between the perceived amount of movement of the central target and the parameters of the dynamic properties of the vergence response. CONCLUSIONS: Peripheral disparity can modulate the dynamics of the initial vergence response to a central disparity and is probably independent of the perception of motion in depth.

Adult↗

Visual requirements for safety and mobility of older drivers.

Efforts to assess visual deterioration with increasing age, coupled with new mechanisms proposed to limit the exposure of visually impaired drivers to driving risks, have emerged in response to the increase in older drivers. Visual functions discussed in this context include static acuity (photopic, mesopic, and in the presence of glare), dynamic visual acuity, visual field, contrast sensitivity, and motion perception. Exposure control mechanisms discussed include alternative periodic vision testing strategies, visual training, and environmental and vehicular modifications to accommodate the older driver. Finally, relevant research needs are addressed.

Aging↗

A modeling approach to the human spatial orientation system.

The human spatial orientation system is highly complex and nonlinear. It is difficult, therefore, to arrive at an unequivocal model of the underlying processing by merely combining the known elementary mechanisms ("bottom-up" approach); additional "top-down" concepts are required to narrow the choice between several formally equivalent solutions. We here suggest a concept in which sensorimotor control is based on a meta-level that provides an internal representation of the physical stimuli acting upon a subject (e.g., tilt of the support surface), whereas the classic reflex concept essentially proceeds from a direct coupling between physiological stimuli, sensors and actuators. At the hypothesized meta-level, the axial body segments are represented as a stack of superimposed platforms with the lowermost platform (generally the feet) riding on a support surface that acts as the buttress for the subject's active movements. From the sensory point of view, this stack constitutes a system of nested references. This concept explains data from various experiments dealing with self- and object motion perception and body stabilization in a more exhaustive way than does the classic concept. In our view, it provides a robust, flexible, and modular framework for perception and action in space.

Humans↗

The critical role of velocity storage in production of motion sickness.

We propose that motion sickness is mediated through the orientation properties of velocity storage in the vestibular system that tend to align eye velocity produced by the angular vestibulo-ocular reflex (aVOR) with gravito-inertial acceleration (GIA). (GIA is the sum of the linear accelerations acting on the head. In the absence of translational accelerations, gravity is the GIA.) We further postulate that motion sickness produced by cross-coupled vestibular stimulation can be characterized by a metric composed of the disparity between the axis of eye rotation and the GIA, the strength of the response to angular motion, and the response duration, as determined by the central vestibular time constant, that is, by the time constant of velocity storage. The nodulus and uvula of the vestibulocerebellum are likely to be the central sites where the disparity is sensed, where the vestibular time constants are habituated, and where links are made to the autonomic system to produce the symptoms and signs.

Adult↗

Vestibular processing in human paramedian precuneus as shown by electrical cortical stimulation.

The authors describe a 16-year-old patient with recurrent episodes of epileptic linear self-motion perception and occasional body tilts. Intracranial seizure monitoring located the seizure onset, caused by a circumscribed ependymoma, in the right paramedian precuneus. Electrical cortical stimulation of this area could reproduce the same vestibular sensations, which ceased after lesionectomy. The findings implicate the paramedian area of the precuneus in the processing of static and dynamic vestibular, probably otolithic, information.

Adolescent↗

Responses to animated contours of neurons in visual cortex area 18 of the cat.

Given that cells in visual cortical area 18 in cats encode information of complex shapes, in addition to conventional stimuli like bars and gratings, we studied the capability of single cells in this area to 'identify' animated contours. The recorded cells were not selective to specific animated contours, whereas they were highly sensitive to the contour's degradation and to the orientation of its elements. The results indicate that cells in area 18 can encode information about many characteristics of complex animated patterns. The findings suggest the existence of a contour abstracting mechanism, which needs further study.

Animals↗

Conflict-dependent gain control in area VIP during visual-vestibular self-motion processing.

Visual and vestibular signals are continuously integrated to estimate self-motion, yet these sensory cues are often inconsistent under natural conditions. How cortical circuits regulate multisensory interactions under cue conflict while preserving stable heading representations remains poorly understood. Here, we recorded neurons in male macaque ventral intraparietal area (VIP) during passive movement stimulation while systematically varying visual-vestibular heading offsets. VIP neurons exhibited strong conflict-sensitive gain modulation: congruent cues enhanced neuronal responses, whereas increasing cue offsets progressively suppressed response gain. This effect was observed not only in multisensory neurons but also in neurons classified as predominantly visual or vestibular, indicating widespread cross-modal interactions across the population. In contrast, preferred-heading shifts remain modest, suggesting that cue conflict primarily modulated response gain rather than altering heading tuning. Despite substantial suppression at the single-neuron level under large cue offsets, population Fisher information was largely preserved, indicating robust heading discriminability. Further analyses revealed flexible sensory weighting in VIP, with visual and vestibular contributions shifting as cue conflict increased. Finally, a feedforward-gated normalization model substantially improved the characterization of VIP responses by allowing cue conflict to dynamically regulate the effective normalization pool, thereby capturing both multisensory enhancement at small visual-vestibular heading offset and suppression under large cue conflict. Together, these findings show that VIP exhibits conflict-dependent regulation of multisensory gain, preserving robust self-motion representations under sensory conflict.Significance statement Visual and vestibular cues are often misaligned in natural environments, creating a challenge for accurate self-motion perception. We demonstrate that neurons in the macaque ventral intraparietal area (VIP) dynamically adjust multisensory gain according to the degree of visual-vestibular conflict. As the visual-vestibular heading offset increases, neuronal responses are progressively enhanced or suppressed, while population coding of heading direction remains largely preserved. A conflict-sensitive normalization model accounts for these response dynamics and outperforms traditional multisensory integration models, suggesting that VIP implements adaptive gain-control computations to regulate interactions between visual and vestibular signals. These results identify a cortical mechanism that links sensory conflict detection to robust perceptual coding, advancing our understanding of multisensory processing in the brain.

Journal Article↗