Effects Of Fixational Eye Movements Research Articles

The effect of fixational eye movements on the flicker-defined edge detection

The effect of fixational eye movements on the flicker-defined edge detection

Effect of fixational eye movements in corneal topography measurements with optical coherence tomography.

There is an increasing interest in applying optical coherence tomography (OCT) to quantify the topography of ocular structures. However, in its most usual configuration, OCT data is acquired sequentially while a beam is scanned through the region of interest, and the presence of fixational eye movements can affect the accuracy of the technique. Several scan patterns and motion correction algorithms have been proposed to minimize this effect, but there is no consensus on the ideal parameters to obtain a correct topography. We have acquired corneal OCT images with raster and radial patterns, and modeled the data acquisition in the presence of eye movements. The simulations replicate the experimental variability in shape (radius of curvature and Zernike polynomials), corneal power, astigmatism, and calculated wavefront aberrations. The variability of the Zernike modes is highly dependent on the scan pattern, with higher variability in the direction of the slow scan axis. The model can be a useful tool to design motion correction algorithms and to determine the variability with different scan patterns.

A computational observer model of spatial contrast sensitivity: Effects of photocurrent encoding, fixational eye movements, and inference engine.

We have recently shown that the relative spatial contrast sensitivity function (CSF) of a computational observer operating on the cone mosaic photopigment excitations of a stationary retina has the same shape as human subjects. Absolute human sensitivity, however, is 5- to 10-fold lower than the computational observer. Here we model how additional known features of early vision affect the CSF: fixational eye movements and the conversion of cone photopigment excitations to cone photocurrents (phototransduction). For a computational observer that uses a linear classifier applied to the responses of a stimulus-matched linear filter, fixational eye movements substantially change the shape of the CSF by reducing sensitivity above 10 c/deg. For a translation-invariant computational observer that operates on the squared response of a quadrature-pair of linear filters, the CSF shape is little changed by eye movements, but there is a two fold reduction in sensitivity. Phototransduction dynamics introduce an additional two fold sensitivity decrease. Hence, the combined effects of fixational eye movements and phototransduction bring the absolute CSF of the translation-invariant computational observer to within a factor of 1 to 2 of the human CSF. We note that the human CSF depends on processing of the retinal representation by many thalamo-cortical neurons, which are individually quite noisy. Our modeling suggests that the net effect of post-retinal noise on contrast-detection performance, when considered at the neural population and behavioral level, is quite small: The inference mechanisms that determine the CSF, presumably in cortex, make efficient use of the information carried by the cone photocurrents of the fixating eye.

The effects of fixational eye movements on population responses in V1. Keynote at the 20th European Conference on Eye Movements in Alicante, September 22, 2019.

During visual fixation, the eyes make small and fast movements known as microsaccades (MSs). The effects of MSs on neural activity in the visual cortex are not well understood. Utilizing voltage-sensitive dye imaging, we imaged the spatiotemporal patterns of neuronal responses induced by MSs in early visual cortices of behaving monkeys.Our results reveal a continuous “visual instability” during fixation: while the visual stimulus moves over the retina with each MS, the neuronal activity in V1 ‘hops’ within the retinotopic map, as dictated by the MS parameters. Neuronal modulations induced by MSs are characterized by neural suppression followed by neural enhancement and increased synchronization. The suppressed activity may underlie the suppressed perception during MSs whereas the late enhancement may facilitate the processing of new incoming image information. Moreover, the instability induced by MSs applies also to neural correlates of visual perception processes such as figure-ground (FG) segregation, which appear to develop faster after fixational saccades.Video stream: https://vimeo.com/362367119

Reduced amblyopic eye fixation stability cannot be simulated using retinal-defocus-induced reductions in visual acuity

Amblyopia is associated with impaired visual acuity (VA) and reduced fixation stability (FS). To assess whether impaired VA may cause reduced FS, the effects of retinal-defocus-induced visual acuity reductions on FS were measured in observers with amblyopia and controls. Fixational eye movements were measured in 8 patients with amblyopia and 12 controls. Monocular near VA of a subset of controls (n = 5) was then varied from 20/20 to 20/100 using convex lenses. The amblyopia group completed three monocular conditions; 1) amblyopic eye fixating, 2) fellow eye fixating and 3) fellow eye fixating with VA reduced to match the amblyopic eye. Fixational eye movements were quantified using bivariate contour ellipse area (BCEA) and microsaccadic amplitude. Amblyopic eye BCEA was significantly larger with increased microsaccadic amplitude compared to the fellow eye and control eyes. BCEA and VA were positively correlated for amblyopic eyes. VA impairments induced by retinal defocus did not reduce FS in controls or the fellow eye of observers with amblyopia, even when fellow eye VA was matched to that of the amblyopic eye. This suggests that reduced FS in amblyopic eyes cannot be simulated by acute VA reductions. Therefore, reduced amblyopic eye FS may not be a direct consequence of the VA loss alone. As in previous studies, a correlation between BCEA and VA for amblyopic eyes was observed. This relationship could be due to a third, mediating variable or an effect of fixational eye movements on VA.

Visual Discomfort From Flash Afterimages of Riloid Patterns.

Op-art-based stimuli have been shown to be uncomfortable, possibly due to a combination of fixational eye movements (microsaccades) and excessive cortical responses. Efforts have been made to measure illusory phenomena arising from these stimuli in the absence of microsaccades, but there has been no attempt thus far to decouple the effects of the cortical response from the effect of fixational eye movements. This study uses flash afterimages to stabilise the image on the retina and thus reduce the systematic effect of eye movements, in order to investigate the role of the brain in discomfort from op-art-based stimuli. There was a relationship between spatial frequency and the magnitude of the P300 response, showing a similar pattern to that of discomfort judgements, which suggests that there might be a role of discomfort and excessive neural responses independently from the effects of microsaccades.

Primate area V1: largest response gain for receptive fields in the straight-ahead direction.

Although neuronal responses in behaving monkeys are typically studied while the monkey fixates straight ahead, it is known that eye position modulates responses of visual neurons. The modulation has been found to enhance neuronal responses when the receptive field is placed in the straight-ahead position for neurons receiving input from the peripheral but not the central retina. We studied the effect of eye position on the responses of V1 complex cells receiving input from the central retina (1.1-5.7° eccentricity) while minimizing the effect of fixational eye movements. Contrast response functions were obtained separately with drifting light and dark bars. Data were fit with the Naka-Rushton equation: r(c)=Rmax×c/(c+c50)+s, where r(c) is mean spike rate at contrast c, Rmax is the maximum response, c50 is the contrast that elicits half of Rmax, and s is the spontaneous activity. Contrast sensitivity as measured by c50 was not affected by eye position. For dark bars, there was a statistically significant decline in the normalized Rmax with increasing deviation from straight ahead. Data for bright bars showed a similar trend with a less rapid decline. Our results indicate that neurons representing the central retina show a bias for the straight-ahead position resulting from modulation of the response gain without an accompanying modulation of contrast sensitivity. The modulation is especially obvious for dark stimuli, which might be useful for directing attention to hazardous situations such as dark holes or shadows concealing important objects (Supplement 1: Video Abstract, Supplemental digital content 1, http://links.lww.com/WNR/A295).

Temporal Encoding of Spatial Information during Active Visual Fixation

Humans and other species continually perform microscopic eye movements, even when attending to a single point. These movements, which include drifts and microsaccades, are under oculomotor control, elicit strong neural responses, and have been thought to serve important functions. The influence of these fixational eye movements on the acquisition and neural processing of visual information remains unclear. Here, we show that during viewing of natural scenes, microscopic eye movements carry out a crucial information-processing step: they remove predictable correlations in natural scenes by equalizing the spatial power of the retinal image within the frequency range of ganglion cells' peak sensitivity. This transformation, which had been attributed to center-surround receptive field organization, occurs prior to any neural processing and reveals a form of matching between the statistics of natural images and those of normal eye movements. We further show that the combined effect of microscopic eye movements and retinal receptive field organization is to convert spatial luminance discontinuities into synchronous firing events, beginning the process of edge detection. Thus, microscopic eye movements are fundamental to two goals of early visual processing: redundancy reduction and feature extraction.

The effect of fixational eye movements on fixation identification with a dispersion-based fixation detection algorithm

Gaze data of 31 participants of a memory recall experiment was analyzed and the I-DT dispersion based algorithm of Salvucci and Goldberg (2000) was used to identify fixations. It was found that individuals differ considerably with regard to the stability of eye gaze and that fixational eye movements affect the accuracy of fixation identification and the optimum dispersion threshold. It was also found that fixation radius and the distance between the points in a fixation that are the furthest apart are the most reliable metrics for a dispersion-based fixation identification algorithm. Finally, it is argued that the correct setting of dispersion threshold is of utmost importance, especially if the participants are not homogeneous with regard to gaze stability.

Eye Position Compensation Improves Estimates of Response Magnitude and Receptive Field Geometry in Alert Monkeys

Studies of visual function in behaving subjects require that stimuli be positioned reliably on the retina in the presence of eye movements. Fixational eye movements scatter stimuli about the retina, inflating estimates of receptive field dimensions, reducing estimates of peak responses, and blurring maps of receptive field subregions. Scleral search coils are frequently used to measure eye position, but their utility for correcting the effects of fixational eye movements on receptive field maps has been questioned. Using eye coils sutured to the sclera and preamplifiers configured to minimize cable artifacts, we reexamined this issue in two rhesus monkeys. During repeated fixation trials, the eye position signal was used to adjust the stimulus position, compensating for eye movements and correcting the stimulus position to place it at the desired location on the retina. Estimates of response magnitudes and receptive field characteristics in V1 and in LGN were obtained in both compensated and uncompensated conditions. Receptive fields were narrower, with steeper borders, and response amplitudes were higher when eye movement compensation was used. In sum, compensating for eye movements facilitated more precise definition of the receptive field. We also monitored horizontal vergence over long sequences of fixation trials and found the variability to be low, as expected for this precise behavior. Our results imply that eye coil signals can be highly accurate and useful for optimizing visual physiology when rigorous precautions are observed.

Effects of fixational eye movements on retinal ganglion cell responses: a modelling study

Visual response properties of retinal ganglion cells (GCs), the retinal output neurons, are shaped by numerous processes and interactions within the retina. In particular, amacrine cells are known to form microcircuits that affect GC responses in specific ways. So far, relatively little is known about the influence of retinal processing on GC responses under naturalistic viewing conditions, in particular in the presence of fixational eye movements. Here we used a detailed model of the mammalian retina to investigate possible effects of fixational eye movements on retinal GC activity. Populations of linear, sustained (parvocellular, PC) and nonlinear, transient (magnocellular, MC) GCs were simulated during fixation of a star-shaped stimulus, and two distinct effects were found: (1) a fading of complete wedges of the star and (2) an apparent splitting of stimulus lines. Both effects only occur in MC-cells, and an analysis shows that fading is caused by an expression of the aperture problem in retinal GCs, and the splitting effect by spatiotemporal nonlinearities in the MC-cell receptive field. These effects strongly resemble perceived instabilities during fixation of the same stimulus, and we propose that these illusions may have a retinal origin. We further suggest that in this case two parallel retinal streams send conflicting, rather than complementary, information to the higher visual system, which here leads to a dominant influence of the MC pathway. Similar situations may be common during natural vision, since retinal processing involves numerous nonlinearities.

High Response Reliability of Neurons in Primary Visual Cortex (V1) of Alert, Trained Monkeys

The reliability of neuronal responses determines the resources needed to represent the external world and constrains the nature of the neural code. Studies of anesthetized animals have indicated that neuronal responses become progressively more variable as information travels from the retina to the cortex. These results have been interpreted to indicate that perception must be based on pooling across relatively large numbers of cells. However, we find that in alert monkeys, responses in primary visual cortex (V1) are as reliable as the inputs from the retina and the thalamus. Moreover, when the effects of fixational eye movements were minimized, response variability (variance/mean - Fano factor, FF) in all V1 layers was low. When presenting optimal stimuli, the median FF was 0.3. High variability, FF approximately 1, was found only near threshold. Our results suggest that in natural vision, suprathreshold perception can be based on small numbers of optimally stimulated cells.