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Dive into the research topics where Andrew T. Rider is active.

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Featured researches published by Andrew T. Rider.


Journal of Vision | 2009

Motion-induced position shifts in global dynamic Gabor arrays.

Andrew T. Rider; Peter W. McOwan; Alan Johnston

Objects in motion appear shifted in space. For global motion stimuli we can ask whether the shift depends on the local or global motion. We constructed arrays of randomly oriented Gaussian enveloped drifting sine gratings (dynamic Gabors) whose speed was set such that the normal component of motion was consistent with a single global velocity. The array appears shifted in space in the direction of the global motion. The size of the shift is the same as for arrays of uniformly oriented dynamic Gabors that are moving in the same direction at the same global speed. Arrays made up of vertically oriented gratings whose speeds were set to the horizontal component of the random array elements were shifted less far. This shows that motion-induced position shifts of coherently moving surface patches are generated after the completion of the global motion computation.


Journal of Vision | 2017

Hue shifts produced by temporal asymmetries in chromatic signals depend on the alignment of the first and second harmonics

Andrew Stockman; G. Bruce Henning; Peter West; Andrew T. Rider; Caterina Ripamonti

When M- or L-cone-isolating sawtooth waveforms flicker at frequencies between 4 and 13.3 Hz, there is a mean hue shift in the direction of the shallower sawtooth slope. Here, we investigate how this shift depends on the alignment of the first and second harmonics of sawtooth-like waveforms. Below 4 Hz, observers can follow hue variations caused by both harmonics, and reliably match reddish and greenish excursions. At higher frequencies, however, the hue variations appear as chromatic flicker superimposed on a steady light, the mean hue of which varies with second-harmonic alignment. Observers can match this mean hue against a variable-duty-cycle rectangular waveform and, separately, set the alignment at which the mean hue flips between reddish and greenish. The maximum hue shifts were approximately frequency independent and occurred when the peaks or troughs of the first and second harmonics roughly aligned at the visual input-consistent with the hue shifts being caused by an early instantaneous nonlinearity that saturates larger hue excursions. These predictions, however, ignore phase delays introduced within the chromatic pathway between its input and the nonlinearity that produces the hue shifts. If the nonlinearity follows the substantial filtering implied by the chromatic temporal contrast-sensitivity function, phase delays will alter the alignment of the first and second harmonics such that at the nonlinearity, the waveforms that produce the maximum hue shifts might well be those with the largest differences in rising and falling slopes-consistent with the hue shifts being caused by a central nonlinearity that limits the rate of hue change.


Journal of Vision | 2017

Linear–nonlinear models of the red–green chromatic pathway

Andrew Stockman; G. Bruce Henning; Andrew T. Rider

The mean hue of flickering waveforms comprising only the first two harmonics depends on their temporal alignment. We evaluate explanatory models of this hue-shift effect using previous data obtained using L- and M-cone-isolating stimuli together with chromatic sensitivity and hue discrimination data. The key questions concerned what type of nonlinearity produced the hue shifts, and where the nonlinearities lay with respect to the early band-pass and late low-pass temporal filters in the chromatic pathways. We developed two plausible models: (a) a slew-rate limited nonlinearity that follows both early and late filters, and (b) a half-wave rectifying nonlinearity-consistent with the splitting of the visual input into ON- and OFF-channels-that lies between the early and late filters followed by a compressive nonlinearity that lies after the late filter.


Journal of Vision | 2014

Asymmetric global motion integration in drifting Gabor arrays

Andrew T. Rider; Peter W. McOwan; Alan Johnston

We examined how ambiguous motion signals are integrated over space to support the unambiguous perception of global motion. The motion of a Gaussian windowed drifting sine grating (Gabor) is consistent with an infinite number of grating velocities. To extract the consistent global motion of multi-Gabor arrays, the visual system must integrate ambiguous motion signals from disparate regions of visual space. We found an interaction between spatial arrangement and global motion integration in this process. Linear arrays of variably oriented Gabor elements appeared to move more slowly, reflecting suboptimal integration, when the direction of global translation was orthogonal to the line as opposed to along it. Circular arrays of Gabor elements appeared to move more slowly when the global motion was an expansion or contraction rather than a rotation. However, there was no difference in perceived speed for densely packed annular arrays for these global motion pattern directions. We conclude that the region over which ambiguous motion is integrated is biased in the direction of global motion, and the concept of the association field, held to link like elements along a contour, needs to be extended to include global motion computation over disparate elements referencing the same global motion.


Journal of Experimental Child Psychology | 2018

Semantic content outweighs low-level saliency in determining children’s and adults’ fixation of movies

Andrew T. Rider; Antoine Coutrot; Elizabeth Pellicano; Steven C. Dakin; Isabelle Mareschal

Highlights • Content outweighs saliency when watching films.• Variance between eye movements decreases with age.• Gaze patterns show similar (qualitative) strategies across development.


Investigative Ophthalmology & Visual Science | 2017

The pattern of retinal ganglion cell loss in OPA1-related autosomal dominant optic atrophy inferred from temporal, spatial, and chromatic sensitivity losses

Anna Majander; Catarina João; Andrew T. Rider; G. Bruce Henning; Marcela Votruba; Anthony T. Moore; Patrick Yu-Wai-Man; Andrew Stockman

Purpose Progressive retinal ganglion cell (RGC) loss is the pathological hallmark of autosomal dominant optic atrophy (DOA) caused by pathogenic OPA1 mutations. The aim of this study was to conduct an in-depth psychophysical study of the visual losses in DOA and to infer any selective vulnerability of visual pathways subserved by different RGC subtypes. Methods We recruited 25 patients carrying pathogenic OPA1 mutations and age-matched healthy individuals. Spatial contrast sensitivity functions (SCSFs) and chromatic contrast sensitivity were quantified, the latter using the Cambridge Colour Test. In 11 patients, long (L) and short (S) wavelength–sensitive cone temporal acuities were measured as a function of target illuminance, and L-cone temporal contrast sensitivity (TCSF) as a function of temporal frequency. Results Spatial contrast sensitivity functions were abnormal, with the loss of sensitivity increasing with spatial frequency. Further, the highest L-cone temporal acuity fell on average by 10 Hz and the TCSFs by 0.66 log10 unit. Chromatic thresholds along the protan, deutan, and tritan axes were 8, 9, and 14 times higher than normal, respectively, with losses increasing with age and S-cone temporal acuity showing the most significant age-related decline. Conclusions Losses of midget parvocellular, parasol magnocellular, and bistratified koniocellular RGCs could account for the losses of high spatial frequency sensitivity and protan and deutan sensitivities, high temporal frequency sensitivity, and S-cone temporal and tritan sensitivities, respectively. The S-cone–related losses showed a significant deterioration with increasing patient age and could therefore prove useful biomarkers of disease progression in DOA.


Journal of Vision | 2016

Multiple-stage ambiguity in motion perception reveals global computation of local motion directions

Andrew T. Rider; Shin'ya Nishida; Alan Johnston

The motion of a 1D image feature, such as a line, seen through a small aperture, or the small receptive field of a neural motion sensor, is underconstrained, and it is not possible to derive the true motion direction from a single local measurement. This is referred to as the aperture problem. How the visual system solves the aperture problem is a fundamental question in visual motion research. In the estimation of motion vectors through integration of ambiguous local motion measurements at different positions, conventional theories assume that the object motion is a rigid translation, with motion signals sharing a common motion vector within the spatial region over which the aperture problem is solved. However, this strategy fails for global rotation. Here we show that the human visual system can estimate global rotation directly through spatial pooling of locally ambiguous measurements, without an intervening step that computes local motion vectors. We designed a novel ambiguous global flow stimulus, which is globally as well as locally ambiguous. The global ambiguity implies that the stimulus is simultaneously consistent with both a global rigid translation and an infinite number of global rigid rotations. By the standard view, the motion should always be seen as a global translation, but it appears to shift from translation to rotation as observers shift fixation. This finding indicates that the visual system can estimate local vectors using a global rotation constraint, and suggests that local motion ambiguity may not be resolved until consistencies with multiple global motion patterns are assessed.


Clinical Ophthalmology | 2016

Psychophysical measures of visual function and everyday perceptual experience in a case of congenital stationary night blindness

Jocelyn Cammack; John Whight; Vinette Cross; Andrew T. Rider; Andrew R. Webster; Andrew Stockman

An appreciation of the relation between laboratory measures of visual deficit and everyday perceptual experience is fundamental to understanding the impact of a visual condition on patients and so to a fuller characterization of the disorder. This study aims to understand better the interpretative processes by which modified sensory information is perceived by a patient with congenital stationary night blindness and the adaptive strategies that are devised to deal with their measurable visual loss. Psychophysical measurements of temporal resolution, spectral sensitivity, and color discrimination were conducted on a 78-year-old male patient with the condition, who was also interviewed at length about the ways in which his diagnosis affected his daily life. Narrative analysis was employed to identify the relation between his subjective perceptual experiences and functional deficits in identifiable components of the visual system. Psychophysical measurements indicated a complete lack of rod perception and substantially reduced cone sensitivity. Two particular effects of this visual loss emerged during interviews: 1) the development of navigational techniques that relied on light reflections and point sources of light and 2) a reluctance to disclose the extent of visual loss and resulting lifelong psychosocial consequences. This study demonstrates the valuable complementary role that rich descriptive patient testimony can play, in conjunction with laboratory and clinical measurements, in more fully characterizing a disorder and in reaching a more complete understanding of the experience of vision loss. It also evidences the particular suitability of filmmaking techniques as a means of accessing and communicating subjective patient experience.


Proceedings of the National Academy of Sciences of the United States of America | 2018

Harmonics added to a flickering light can upset the balance between ON and OFF pathways to produce illusory colors

Andrew T. Rider; G. Bruce Henning; Rhea T. Eskew; Andrew Stockman

Significance By varying the temporal waveforms of complex flickering stimuli, we can produce alterations in their mean color that can be predicted by a physiologically based model of visual processing. The model highlights the perceptual effects of a well-known feature of most visual pathways, namely the early separation of visual signals into increments and decrements. The role of this separation in improving the efficiency and sensitivity of the visual system has been discussed before, but its effect on perception has been neglected. The application of a model incorporating half-wave rectification offers an exciting psychophysical method for investigating the inner workings of the human visual system. The neural signals generated by the light-sensitive photoreceptors in the human eye are substantially processed and recoded in the retina before being transmitted to the brain via the optic nerve. A key aspect of this recoding is the splitting of the signals within the two major cone-driven visual pathways into distinct ON and OFF branches that transmit information about increases and decreases in the neural signal around its mean level. While this separation is clearly important physiologically, its effect on perception is unclear. We have developed a model of the ON and OFF pathways in early color processing. Using this model as a guide, we can produce imbalances in the ON and OFF pathways by changing the shapes of time-varying stimulus waveforms and thus make reliable and predictable alterations to the perceived average color of the stimulus—although the physical mean of the waveforms does not change. The key components in the model are the early half-wave rectifying synapses that split retinal photoreceptor outputs into the ON and OFF pathways and later sigmoidal nonlinearities in each pathway. The ability to systematically vary the waveforms to change a perceptual quality by changing the balance of signals between the ON and OFF visual pathways provides a powerful psychophysical tool for disentangling and investigating the neural workings of human vision.


Investigative Ophthalmology & Visual Science | 2017

The Pattern of Retinal Ganglion Cell Loss in OPA1-Related Autosomal Dominant Optic Atrophy Inferred From Temporal, Spatial, and Chromatic Sensitivity LossesVisual Losses Related to Retinal Ganglion Cell Losses in DOA

Anna Majander; Catarina João; Andrew T. Rider; G. Bruce Henning; Marcela Votruba; Anthony T. Moore; Patrick Yu-Wai-Man; Andrew Stockman

Purpose Progressive retinal ganglion cell (RGC) loss is the pathological hallmark of autosomal dominant optic atrophy (DOA) caused by pathogenic OPA1 mutations. The aim of this study was to conduct an in-depth psychophysical study of the visual losses in DOA and to infer any selective vulnerability of visual pathways subserved by different RGC subtypes. Methods We recruited 25 patients carrying pathogenic OPA1 mutations and age-matched healthy individuals. Spatial contrast sensitivity functions (SCSFs) and chromatic contrast sensitivity were quantified, the latter using the Cambridge Colour Test. In 11 patients, long (L) and short (S) wavelength–sensitive cone temporal acuities were measured as a function of target illuminance, and L-cone temporal contrast sensitivity (TCSF) as a function of temporal frequency. Results Spatial contrast sensitivity functions were abnormal, with the loss of sensitivity increasing with spatial frequency. Further, the highest L-cone temporal acuity fell on average by 10 Hz and the TCSFs by 0.66 log10 unit. Chromatic thresholds along the protan, deutan, and tritan axes were 8, 9, and 14 times higher than normal, respectively, with losses increasing with age and S-cone temporal acuity showing the most significant age-related decline. Conclusions Losses of midget parvocellular, parasol magnocellular, and bistratified koniocellular RGCs could account for the losses of high spatial frequency sensitivity and protan and deutan sensitivities, high temporal frequency sensitivity, and S-cone temporal and tritan sensitivities, respectively. The S-cone–related losses showed a significant deterioration with increasing patient age and could therefore prove useful biomarkers of disease progression in DOA.

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Andrew Stockman

UCL Institute of Ophthalmology

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G. Bruce Henning

UCL Institute of Ophthalmology

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Alan Johnston

University of Nottingham

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Bruce Henning

UCL Institute of Ophthalmology

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Caterina Ripamonti

UCL Institute of Ophthalmology

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Peter West

UCL Institute of Ophthalmology

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Catarina João

University College London

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Peter W. McOwan

Queen Mary University of London

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