Auditory Motion Induces Directionally Dependent Receptive Field Shifts in Inferior Colliculus Neurons

1998 ◽  
Vol 79 (4) ◽  
pp. 2040-2062 ◽  
Author(s):  
Willard W. Wilson ◽  
William E. O'Neill
Keyword(s):  
Receptive Field ◽  
Inferior Colliculus ◽  
Apparent Motion ◽  
Target Location ◽  
Receptive Fields ◽  
Silent Interval ◽  
Auditory Motion ◽  
Motion Direction ◽  
Motion Sequence ◽  
And Shifts

Wilson, Willard W. and William E. O'Neill. Auditory motion induces directionally dependent receptive field shifts in inferior colliculus neurons. J. Neurophysiol. 79: 2040–2062, 1998. This research focused on the response of neurons in the inferior colliculus of the unanesthetized mustached bat, Pteronotus parnelli, to apparent auditory motion. We produced the apparent motion stimulus by broadcasting pure-tone bursts sequentially from an array of loudspeakers along horizontal, vertical, or oblique trajectories in the frontal hemifield. Motion direction had an effect on the response of 65% of the units sampled. In these cells, motion in opposite directions produced shifts in receptive field locations, differences in response magnitude, or a combination of the two effects. Receptive fields typically were shifted opposite the direction of motion (i.e., units showed a greater response to moving sounds entering the receptive field than exiting) and shifts were obtained to horizontal, vertical, and oblique motion orientations. Response latency also shifted as a function of motion direction, and stimulus locations eliciting greater spike counts also exhibited the shortest neural latency. Motion crossing the receptive field boundaries appeared to be both necessary and sufficient to produce receptive field shifts. Decreasing the silent interval between successive stimuli in the apparent motion sequence increased both the probability of obtaining a directional effect and the magnitude of receptive field shifts. We suggest that the observed directional effects might be explained by “spatial masking,” where the response of auditory neurons after stimulation from particularly effective locations in space would be diminished. The shift in auditory receptive fields would be expected to shift the perceived location of a moving sound and may explain shifts in localization of moving sources observed in psychophysical studies. Shifts in perceived target location caused by auditory motion might be exploited by auditory predators such as Pteronotus in a predictive tracking strategy to capture moving insect prey.

Spatial Receptive Fields of Inferior Colliculus Neurons to Auditory Apparent Motion in Free Field

2001 ◽  
Vol 85 (1) ◽  
pp. 23-33 ◽  
Author(s):  
Neil J. Ingham ◽  
Heledd C. Hart ◽  
David McAlpine
Keyword(s):  
Inferior Colliculus ◽  
Apparent Motion ◽  
Free Field ◽  
Receptive Fields ◽  
Motion Processing ◽  
Auditory Motion ◽  
Motion Cues ◽  
Discharge Rates ◽  
Angular Velocities ◽  
Sequential Activation

We examined responses from 91 single-neurons in the inferior colliculus (IC) of anesthetized guinea pigs to auditory apparent motion in the free field. Apparent motion was generated by presenting 100-ms tone bursts, separated by 50-ms silent intervals, at consecutive speaker positions in an array of 11 speakers, positioned in an arc ±112.5° around midline. Most neurons demonstrated discrete spatial receptive fields (SRFs) to apparent motion in the clockwise and anti-clockwise directions. However, SRFs showed marked differences for apparent motion in opposite directions. In virtually all neurons, mean best azimuthal positions for SRFs to opposite directions occurred at earlier positions in the motion sweep, producing receptive fields to the two directions of motion that only partially overlapped. Despite this, overall spike counts to the two directions were similar for equivalent angular velocities. Responses of 28 neurons were recorded to stimuli with different duration silent intervals between speaker presentations, mimicking different apparent angular velocities. Increasing the stimulus off time increased neuronal discharge rates, particularly at later portions of the apparent motion sweep, and reduced the differences in the SRFs to opposite motion directions. Consequently SRFs to both directions broadened and converged with decreasing motion velocity. This expansion was most obvious on the outgoing side of the each SRF. Responses of 11 neurons were recorded to short (90°) partially overlapping apparent motion sweeps centered at different spatial positions. Nonoverlapping response profiles were recorded in 9 of the 11 neurons tested and confirmed that responses at each speaker position were dependent on the preceding response history. Together these data are consistent with the suggestion that a mechanism of adaptation of excitation contributes to the apparent sensitivity of IC neurons to auditory motion cues. In addition, the data indicate that the sequential activation of an array of speakers to produce apparent auditory motion may not be an optimal stimulus paradigm to separate the temporal and spatial aspects of auditory motion processing.

Computation of motion direction by quail retinal ganglion cells that have a nonconcentric receptive field

2000 ◽  
Vol 17 (2) ◽  
pp. 263-271 ◽  
Author(s):  
HIROYUKI UCHIYAMA ◽  
TAKAHIDE KANAYA ◽  
SHOICHI SONOHATA
Keyword(s):  
Receptive Field ◽  
Retinal Ganglion Cells ◽  
Japanese Quail ◽  
Ganglion Cells ◽  
Receptive Fields ◽  
Object Motion ◽  
Directional Selectivity ◽  
Retinal Ganglion ◽  
Motion Direction ◽  
Neuronal Mechanisms

One type of retinal ganglion cells prefers object motion in a particular direction. Neuronal mechanisms for the computation of motion direction are still unknown. We quantitatively mapped excitatory and inhibitory regions of receptive fields for directionally selective retinal ganglion cells in the Japanese quail, and found that the inhibitory regions are displaced about 1–3 deg toward the side where the null sweep starts, relative to the excitatory regions. Directional selectivity thus results from delayed transient suppression exerted by the nonconcentrically arranged inhibitory regions, and not by local directional inhibition as hypothesized by Barlow and Levick (1965).

scholarly journals Horizontal connectivity in V1 : Prediction of coherence in contour and motion integration

2021 ◽  
Author(s):  
Yves Fregnac ◽  
Benoit Le Bec ◽  
Xoana G. Troncoso ◽  
Christophe Desbois ◽  
Yannick Passarelli ◽  
...  
Keyword(s):  
Apparent Motion ◽  
Propagation Speed ◽  
Flow Speed ◽  
Contextual Control ◽  
Axial Motion ◽  
Global Motion ◽  
Motion Direction ◽  
Orientation Preference ◽  
Speed Range ◽  
Motion Sequence

This study demonstrates the functional importance of the Surround context relayed laterally in V1 by the horizontal connectivity, in controlling the latency and the gain of the cortical response to the feedforward visual drive. We report here four main findings : 1) a centripetal apparent motion sequence results in a shortening of the spiking latency of V1 cells, when the orientation of the local inducer and the global motion axis are both co-aligned with the RF orientation preference; 2) this contextual effects grows with visual flow speed, peaking at 150-250 degrees per second until matching the propagation speed of horizontal connectivity (0.15-0.25 mm/ms); 3) For this speed range, axial sensitivity of V1 cells is tilted by 90 degrees to become co-aligned with the orientation preference axis; 4) the modulation strength by the surround context correlates with the spatiotemporal coherence of the apparent motion flow. Our results suggest an internally-generated binding process, linking local (orientation /position) and global (motion/direction) features as early as V1. This long-range diffusion process constitutes a plausible substrate in V1 of the human psychophysical bias in speed estimate for collinear motion. Since demonstrated in the anesthetized cat, this novel form of contextual control of the cortical transfer function is a built-in property in V1, whose expression does not require behavioral attention and top-down control from higher cortical areas. We propose that horizontal connectivity participates to the propagation of an internal prediction wave, linking contour co-alignment and global axial motion at an apparent speed in the range of saccadic-like eye-movements.

scholarly journals GABAergic Inhibition Influences Auditory Motion-Direction Sensitivity in Barn Owls

1998 ◽  
Vol 80 (1) ◽  
pp. 172-185 ◽  
Author(s):  
Dirk Kautz ◽  
Hermann Wagner
Keyword(s):  
Inferior Colliculus ◽  
Visual Motion ◽  
Gabaergic Inhibition ◽  
Auditory Motion ◽  
Cellular Mechanisms ◽  
Motion Direction ◽  
Inhibitory Mechanisms ◽  
Barn Owls ◽  
Gaba Antagonist ◽  
Direction Sensitivity

Kautz, Dirk and Hermann Wagner. GABAergic inhibition influences auditory motion-direction sensitivity in barn owls. J. Neurophysiol. 80: 172–185, 1998. Many neurons in the barn owl's inferior colliculus (IC) exhibit auditory motion-direction sensitivity (MDS), i.e., they respond more to motion of a sound source in one direction than to motion in the opposite direction. We investigated the cellular mechanisms underlying the phenomenon of auditory MDS by microiontophoretically applying γ-aminobutyric acid (GABA) or the GABA-antagonist bicuculline methiodide (BMI) while recording from neurons in the owl's midbrain. In most cases GABA reduced the overall firing rate, whereas BMI increased it. In addition, 29% of the motion-direction–sensitive cells completely lost their selectivity for the direction of auditory movement during administration of BMI. It had been proposed that auditory MDS in the owl is due to inhibition. The present results show that GABAergic inhibition plays a role in the strengthening of MDS. We discuss the data within the framework of the acoustic motion detector and with respect to microiontophoretic studies on visual motion detection and on inhibitory mechanisms in the inferior colliculus.

scholarly journals Scrambling the skin: A psychophysical study of adaptation to scrambled tactile apparent motion

PLoS ONE ◽  
2020 ◽  
Vol 15 (12) ◽  
pp. e0227462
Author(s):  
Tatjana Seizova-Cajic ◽  
Sandra Ludvigsson ◽  
Birger Sourander ◽  
Melinda Popov ◽  
Janet L. Taylor
Keyword(s):  
Apparent Motion ◽  
Constant Velocity ◽  
Stimulus Onset ◽  
Object Motion ◽  
Local Motion ◽  
Motion Direction ◽  
Good Test ◽  
Motion Sequence ◽  
Velocity Motion ◽  
Perceived Motion

An age-old hypothesis proposes that object motion across the receptor surface organizes sensory maps (Lotze, 19th century). Skin patches learn their relative positions from the order in which they are stimulated during motion events. We propose that reversing the local motion within a global motion sequence (‘motion scrambling’) provides a good test for this idea, and present results of the first experiment implementing the paradigm. We used 6-point apparent motion along the forearm. In the Scrambled sequence, two middle locations were touched in reversed order (1-2-4-3-5-6, followed by 6-5-3-4-2-1, in a continuous loop). This created a double U-turn within an otherwise constant-velocity motion, as if skin patches 3 and 4 physically swapped locations. The control condition, Orderly, proceeded at constant velocity at inter-stimulus onset interval of 120 ms. The 26.4-minute conditioning (delivered in twenty-four 66-s bouts) was interspersed with testing of perceived motion direction between the two middle tactors presented on their own (sequence 3–4 or 4–3). Our twenty participants reported motion direction. Direction discrimination was degraded following exposure to Scrambled pattern and was 0.31 d’ weaker than following Orderly conditioning (p = .007). Consistent with the proposed role of motion, this could be the beginning of re-learning of relative positions. An alternative explanation is that greater speed adaptation occurred in the Scrambled pattern, raising direction threshold. In future studies, longer conditioning should tease apart the two explanations: our re-mapping hypothesis predicts an overall reversal in perceived motion direction between critical locations (for either motion direction), whereas the speed adaptation alternative predicts chance-level performance at worst, without reversing.

Motion selectivity in macaque visual cortex. II. Spatiotemporal range of directional interactions in MT and V1

1986 ◽  
Vol 55 (6) ◽  
pp. 1328-1339 ◽  
Author(s):  
A. Mikami ◽  
W. T. Newsome ◽  
R. H. Wurtz
Keyword(s):  
Receptive Field ◽  
Apparent Motion ◽  
Receptive Fields ◽  
Direction Selectivity ◽  
Field Size ◽  
Receptive Field Size ◽  
Mt Neurons ◽  
V1 Neurons ◽  
Spatial Interval ◽  
Temporal Intervals

We measured the spatial and temporal limits of directional interactions for 105 directionally selective middle temporal (MT) neurons and 26 directionally selective striate (V1) neurons. Directional interactions were measured using sequentially flashed stimuli in which the spatial and temporal intervals between stimuli were systematically varied over a broad range. A direction index was employed to determine the strength of directional interactions for each combination of spatial and temporal intervals tested. The maximum spatial interval for which directional interactions occurred in a particular neuron was positively correlated with receptive-field size and with retinal eccentricity in both MT and V1. The maximum spatial interval was, on average, three times as large in MT as in V1. The maximum temporal interval for which we obtained directional interactions was similar in MT and V1 and did not vary with receptive-field size or eccentricity. The maximum spatial interval for directional interactions as measured with flashed stimuli was positively correlated with the maximum speed of smooth motion that yielded directional responses. MT neurons were directionally selective for higher speeds than were V1 neurons. These observations indicate that the large receptive fields found in MT permit directional interactions over longer distances than do the more limited receptive fields of V1 neurons. A functional advantage is thereby conferred on MT neurons because they detect directional differences for higher speeds than do V1 neurons. Recent psychophysical studies have measured the spatial and temporal limits for the perception of apparent motion in sequentially flashed visual displays. A comparison of the psychophysical results with our physiological data indicates that the spatiotemporal limits for perception are similar to the limits for direction selectivity in MT neurons but differ markedly from those for V1 neurons. These observations suggest a correspondence between neuronal responses in MT and the short-range process of apparent motion.

scholarly journals Visual performance in behaving cats after prenatal unilateral enucleation

1993 ◽  
Vol 90 (23) ◽  
pp. 11142-11146 ◽  
Author(s):  
S Bisti ◽  
C Trimarchi
Keyword(s):  
Visual Acuity ◽  
Visual Field ◽  
Receptive Field ◽  
Receptive Fields ◽  
Direction Selectivity ◽  
Visual Performance ◽  
Field Size ◽  
Electrophysiological Recordings ◽  
Severe Impairment ◽  
Orientation Columns

Prenatal unilateral enucleation in mammals causes an extensive anatomical reorganization of visual pathways. The remaining eye innervates the entire extent of visual subcortical and cortical areas. Electrophysiological recordings have shown that the retino-geniculate connections are retinotopically organized and geniculate neurones have normal receptive field properties. In area 17 all neurons respond to stimulation of the remaining eye and retinotopy, orientation columns, and direction selectivity are maintained. The only detectable change is a reduction in receptive field size. Are these changes reflected in the visual behavior? We studied visual performance in cats unilaterally enucleated 3 weeks before birth (gestational age at enucleation, 39-42 days). We tested behaviorally the development of visual acuity and, in the adult, the extension of the visual field and the contrast sensitivity. We found no difference between prenatal monocularly enucleated cats and controls in their ability to orient to targets in different positions of the visual field or in their visual acuity (at any age). The major difference between enucleated and control animals was in contrast sensitivity:prenatal enucleated cats present a loss in sensitivity for gratings of low spatial frequency (below 0.5 cycle per degree) as well as a slight increase in sensitivity at middle frequencies. We conclude that prenatal unilateral enucleation causes a selective change in the spatial performance of the remaining eye. We suggest that this change is the result of a reduction in the number of neurones with large receptive fields, possibly due to a severe impairment of the Y system.

Ferrier lecture - Functional architecture of macaque monkey visual cortex

1977 ◽  
Vol 198 (1130) ◽  
pp. 1-59 ◽  
Keyword(s):  
Visual Cortex ◽  
Visual Field ◽  
Receptive Field ◽  
Striate Cortex ◽  
Single Cells ◽  
Ocular Dominance ◽  
Receptive Fields ◽  
Macaque Monkey ◽  
Area 17 ◽  
Orientation Specificity

Of the many possible functions of the macaque monkey primary visual cortex (striate cortex, area 17) two are now fairly well understood. First, the incoming information from the lateral geniculate bodies is rearranged so that most cells in the striate cortex respond to specifically oriented line segments, and, second, information originating from the two eyes converges upon single cells. The rearrangement and convergence do not take place immediately, however: in layer IVc, where the bulk of the afferents terminate, virtually all cells have fields with circular symmetry and are strictly monocular, driven from the left eye or from the right, but not both; at subsequent stages, in layers above and below IVc, most cells show orientation specificity, and about half are binocular. In a binocular cell the receptive fields in the two eyes are on corresponding regions in the two retinas and are identical in structure, but one eye is usually more effective than the other in influencing the cell; all shades of ocular dominance are seen. These two functions are strongly reflected in the architecture of the cortex, in that cells with common physiological properties are grouped together in vertically organized systems of columns. In an ocular dominance column all cells respond preferentially to the same eye. By four independent anatomical methods it has been shown that these columns have the form of vertically disposed alternating left-eye and right-eye slabs, which in horizontal section form alternating stripes about 400 μm thick, with occasional bifurcations and blind endings. Cells of like orientation specificity are known from physiological recordings to be similarly grouped in much narrower vertical sheeet-like aggregations, stacked in orderly sequences so that on traversing the cortex tangentially one normally encounters a succession of small shifts in orientation, clockwise or counterclockwise; a 1 mm traverse is usually accompanied by one or several full rotations through 180°, broken at times by reversals in direction of rotation and occasionally by large abrupt shifts. A full complement of columns, of either type, left-plus-right eye or a complete 180° sequence, is termed a hypercolumn. Columns (and hence hypercolumns) have roughly the same width throughout the binocular part of the cortex. The two independent systems of hypercolumns are engrafted upon the well known topographic representation of the visual field. The receptive fields mapped in a vertical penetration through cortex show a scatter in position roughly equal to the average size of the fields themselves, and the area thus covered, the aggregate receptive field, increases with distance from the fovea. A parallel increase is seen in reciprocal magnification (the number of degrees of visual field corresponding to 1 mm of cortex). Over most or all of the striate cortex a movement of 1-2 mm, traversing several hypercolumns, is accompanied by a movement through the visual field about equal in size to the local aggregate receptive field. Thus any 1-2 mm block of cortex contains roughly the machinery needed to subserve an aggregate receptive field. In the cortex the fall-off in detail with which the visual field is analysed, as one moves out from the foveal area, is accompanied not by a reduction in thickness of layers, as is found in the retina, but by a reduction in the area of cortex (and hence the number of columnar units) devoted to a given amount of visual field: unlike the retina, the striate cortex is virtually uniform morphologically but varies in magnification. In most respects the above description fits the newborn monkey just as well as the adult, suggesting that area 17 is largely genetically programmed. The ocular dominance columns, however, are not fully developed at birth, since the geniculate terminals belonging to one eye occupy layer IVc throughout its length, segregating out into separate columns only after about the first 6 weeks, whether or not the animal has visual experience. If one eye is sutured closed during this early period the columns belonging to that eye become shrunken and their companions correspondingly expanded. This would seem to be at least in part the result of interference with normal maturation, though sprouting and retraction of axon terminals are not excluded.

Organization of striate cortex of alert, trained monkeys (Macaca fascicularis): ongoing activity, stimulus selectivity, and widths of receptive field activating regions

1995 ◽  
Vol 74 (5) ◽  
pp. 2100-2125 ◽  
Author(s):  
D. M. Snodderly ◽  
M. Gur
Keyword(s):  
Receptive Field ◽  
Macaca Fascicularis ◽  
Striate Cortex ◽  
Receptive Fields ◽  
Cortical Processing ◽  
Ongoing Activity ◽  
Fine Detail ◽  
Laminar Distribution ◽  
Maintained Discharge ◽  
Direction Of Movement

1. In alert macaque monkeys, multiunit activity is encountered in an alternating sequence of silent and spontaneously active zones as an electrode is lowered through the striate cortex (V1). 2. Individual neurons that are spontaneously active in the dark usually have a maintained discharge in the light. Because both types of discharge occur in the absence of deliberate stimulation, we call them the "ongoing" activity. The zones with ongoing activity correspond to the cytochrome oxidase (CytOx)-rich geniculorecipient layers 4A, 4C, and 6, whereas the adjacent layers 2/3, 4B, and 5 have little ongoing activity. 3. The widths of receptive field activating regions (ARs) are positively correlated with the cells' ongoing activity. Cells with larger ARs are preferentially located in the CytOx-rich (input) layers, and many are unselective for stimulus orientation. However, approximately 90% of the cells in the silent layers are orientation selective, and they often have small ARs. 4. The laminar distribution of selectivity for orientation and direction of movement in alert animals is consistent with earlier results from anesthetized animals, but the laminar distribution of AR widths differs. In alert macaques, the ARs of direction-selective cells in layer 4B and of orientation-selective cells in layer 5 are among the smallest in V1. 5. Our findings indicate that the input layers of V1 (4A, 4C, and 6) have a diversity of AR widths, including large ones. Cortical processing produces receptive fields in some of the output layers (4B and 5) that are restricted to small ARs with high resolution of spatial position. These results imply potent lateral and/or interlaminar interactions in alert animals in early cortical processing. The diversity of AR widths generated in V1 may contribute to detection of fine detail in the presence of contrasting backgrounds--the early stages of figure-ground discrimination.

Spatio-Temporal Subthreshold Receptive Fields in the Vibrissa Representation of Rat Primary Somatosensory Cortex

1998 ◽  
Vol 80 (6) ◽  
pp. 2882-2892 ◽  
Author(s):  
Christopher I. Moore ◽  
Sacha B. Nelson
Keyword(s):  
Receptive Field ◽  
Somatosensory Cortex ◽  
Rise Time ◽  
Cortical Plasticity ◽  
Temporal Dynamics ◽  
Receptive Fields ◽  
Excitatory Input ◽  
Primary Somatosensory Cortex ◽  
Spatio Temporal ◽  
Sensory Evoked

Moore, Christopher I. and Sacha B. Nelson. Spatio-temporal subthreshold receptive fields in the vibrissa representation of rat primary somatosensory cortex. J. Neurophysiol. 80: 2882–2892, 1998. Whole cell recordings of synaptic responses evoked by deflection of individual vibrissa were obtained from neurons within adult rat primary somatosensory cortex. To define the spatial and temporal properties of subthreshold receptive fields, the spread, amplitude, latency to onset, rise time to half peak amplitude, and the balance of excitation and inhibition of subthreshold input were quantified. The convergence of information onto single neurons was found to be extensive: inputs were consistently evoked by vibrissa one- and two-away from the vibrissa that evoked the largest response (the “primary vibrissa”). Latency to onset, rise time, and the incidence and strength of inhibitory postsynaptic potentials (IPSPs) varied as a function of position within the receptive field and the strength of evoked excitatory input. Nonprimary vibrissae evoked smaller amplitude subthreshold responses [primary vibrissa, 9.1 ± 0.84 (SE) mV, n = 14; 1-away, 5.1 ± 0.5 mV, n = 38; 2-away, 3.7 ± 0.59 mV, n = 22; 3-away, 1.3 ± 0.70 mV, n = 8] with longer latencies (primary vibrissa, 10.8 ± 0.80 ms; 1-away, 15.0 ± 1.2 ms; 2-away, 15.7 ± 2.0 ms). Rise times were significantly faster for inputs that could evoke action potential responses (suprathreshold, 4.1 ± 1.3 ms, n = 8; subthreshold, 12.4 ± 1.5 ms, n = 61). In a subset of cells, sensory evoked IPSPs were examined by deflecting vibrissa during injection of hyperpolarizing and depolarizing current. The strongest IPSPs were evoked by the primary vibrissa ( n = 5/5), but smaller IPSPs also were evoked by nonprimary vibrissae ( n = 8/13). Inhibition peaked by 10–20 ms after the onset of the fastest excitatory input to the cortex. This pattern of inhibitory activity led to a functional reversal of the center of the receptive field and to suppression of later-arriving and slower-rising nonprimary inputs. Together, these data demonstrate that subthreshold receptive fields are on average large, and the spatio-temporal dynamics of these receptive fields vary as a function of position within the receptive field and strength of excitatory input. These findings constrain models of suprathreshold receptive field generation, multivibrissa interactions, and cortical plasticity.

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