This thesis presents two studies that investigate how vision is used to control rapid, compensatory reach-to-grasp reactions. Compensatory grasping reactions were evoked in healthy young adults via unpredictable translations of large platforms on which the subjects stood or walked. The first study tracked natural gaze behaviour during responses to unexpected balance perturbations. It provided evidence that, unlike with voluntary movements, the eyes do not lead the hand during balance recovery – subjects relied on ‘stored’ information from central vision, continuously-available peripheral vision, or a combination of these sources to guide the hand. The second study investigated the efficacy of reliance on peripheral vision to guide rapid reach-to-grasp balance-recovery reactions. Peripheral vision was found to guide reach-to-grasp responses with sufficient accuracy to achieve a functional grasp of a relatively small handhold; however, peripherally-guided movements were slower when the handhold was in the extreme periphery.

This thesis presents two studies that investigate how vision is used to control rapid, compensatory reach-to-grasp reactions. Compensatory grasping reactions were evoked in healthy young adults via unpredictable translations of large platforms on which the subjects stood or walked. The first study tracked natural gaze behaviour during responses to unexpected balance perturbations. It provided evidence that, unlike with voluntary movements, the eyes do not lead the hand during balance recovery – subjects relied on ‘stored’ information from central vision, continuously-available peripheral vision, or a combination of these sources to guide the hand. The second study investigated the efficacy of reliance on peripheral vision to guide rapid reach-to-grasp balance-recovery reactions. Peripheral vision was found to guide reach-to-grasp responses with sufficient accuracy to achieve a functional grasp of a relatively small handhold; however, peripherally-guided movements were slower when the handhold was in the extreme periphery.

yes / Purpose Perimetry is increasingly being used to measure sensitivity at central visual field locations. For many tasks, the central (0°, 0°) location is functionally the most important, however threshold estimates at this location may be affected by masking by the nearby spatial structure of the fixation target. We investigated this effect. Methods First we retrospectively analysed microperimetry (MAIA-2; CenterVue, Padova, Italy) data from 60 healthy subjects, tested on a custom grid with 1° central spacing. We compared sensitivity at (0°, 0°) to the mean sensitivity at the eight adjacent locations. We then prospectively tested 15 further healthy subjects on the same instrument using a cross-shaped test pattern with 1° spacing. Testing was carried out with and without the central fixation target, and sensitivity estimates at (0°, 0°) were compared. We also compared sensitivity at (0°, 0°) to the mean of the adjacent four locations in each condition. Three subjects undertook 10 repeated tests with the fixation target in place to assess within-subject variability of the effect. Results In the retrospective analysis, central sensitivity was median 2.8 dB lower (95% range 0.1–8.8 dB lower, p < 0.0001) than the mean of the adjacent locations. In the prospective study, central sensitivity was median 2.0 dB lower with the fixation target vs without (95% range 0.4–4.7 dB lower, p = 0.0011). With the fixation target in place central sensitivity was median 2.5 dB lower than mean sensitivity of adjacent locations (95% range 0.8–4.2 dB lower, p = 0.0007), whilst without the fixation target there was no difference (mean 0.4 dB lower, S.D. 0.9 dB, p = 0.15). These differences could not be explained by reduced fixation stability. Mean within subject standard deviation in the difference between central and adjacent locations' sensitivity was 1.84 dB for the repeated tests. Conclusions Perimetric sensitivity estimates from the central (0°, 0°) location are, on-average, reduced by 2 to 3 dB, corresponding to a 60–100% increase in stimulus luminance at threshold. This effect can be explained by masking by the nearby fixation target. The considerable within- and between-subject variability in magnitude, and the unknown effects of disease may hamper attempts to compensate threshold estimates for this effect. Clinicians should interpret central perimetric sensitivity estimates with caution, especially in patients with reduced sensitivity due to disease.

Yes / Depictions of vision with AMD in public information material typically show a central region of absolute vision loss. Patients with early and moderate disease frequently do not report this. We aimed to measure how a group of people with AMD perceive everyday scenes in order to produce accurate depictions. We report on six people aged 65-82 years with monocular AMD (visual acuity +0.04 to +1.64 logMAR) and normal vision in the fellow eye. Participants viewed 4 images monocularly, alternating between eyes. The image was digitally altered to approximate participants’ descriptions of their perception with the affected eye. The altered image was viewed with the unaffected eye, and compared with the original image viewed with the affected eye. This was repeated iteratively until a perceptual match was achieved between the modified image/unaffected eye and the original image/affected eye. For five AMD participants with visual acuity +0.04 to +0.50 logMAR the modified images did not resemble those in current public information material. Image modifications required to achieve perceptual similarity with the affected eyes included localised distortion, contrast reduction and blur. Widespread colour desaturation was also required in some cases. One participant with advanced geographic atrophy reported an absolute positive scotoma, similar to existing depictions. Vision in people with AMD may not conform to the common depiction of a central region of absolute vision loss. The accurate representations of AMD patients’ vision produced in this study will enable better understanding of the visual consequences of AMD. / College of Optometrists Postdoctoral Award; National Institute for Health Research Postdoctoral Fellowship

This research is about evaluating vision in the periphery. Peripheral vision is of fundamental importance in the performance of our everyday activities. The aim of this thesis is to develop methods suitable for the evaluation of peripheral vision and to assess how different visual functions vary across the visual field. The results have application both within the field of visual rehabilitation of people with central visual field loss (CFL)and as well as in myopia research. All methods for assessing peripheral vision were implemented with adaptive psychophysical algorithms based on Bayesian statistics. A routine for time-efficient evaluation of peripheral contrast sensitivity was implemented and verified for measurements out to 30° in the visual field. Peripheral vision was evaluated for different properties of the stimuli: sharpness, motion, orientation, and extent. Optical quality was controlled using adaptive optics and/or corrective spectacles specially adapted for the peripheral viewing angle. We found that many peripheral visual functions improved with optical correction, especially in people with CFL. We also found improvements in peripheral contrast sensitivity for low spatial frequencies when stimuli drifted at 5 to 10 Hz; this applies both for people with normal vision and those with CFL. In the periphery, it is easier to see lines that are oriented parallel with respect to the visual field meridian. We have shown that this directional bias is present for both resolution and detection tasks in the periphery, even when the asymmetric optical errors are minimized. For accurate evaluation of peripheral vision, we therefore recommend using gratings that are oriented oblique to the visual  field meridian. The directional bias may have implications in how peripheral image quality affects myopia progression. Another proof that peripheral vision can influence central visual function is the fact that, when the stimulus extent was increased beyond the fovea, the blur in the stimulus was less noticeable. / Denna forskning handlar om att utvärdera synen i periferin. Vår perifera syn är ovärderlig i det dagliga livet. Målsättningen med denna avhandling är dels att utveckla metoder speciellt lämpade för perifer synutvärdering och dels att mäta hur olika synfunktioner varierar över synfältet. Resultaten har tillämpning både inom synrehabilitering för personer med centraltsynfältsbortfall och inom närsynthetsforskning. Adaptiv psykofysisk metodologi baserad på Bayesiansk statistik användes vid all utvärdering av det perifera seendet. Vi implementerade en rutin för tidseffektiv mätning av perifer kontrastkänslighet och verifierade den ut till 30° i synfältet. Den perifera synen utvärderades för olika egenskaper hos objektet: skärpa, rörelse, riktning och utbredning. Skärpan kontrollerades med hjälp av adaptiv optik och/eller glasögonkorrektion speciellt anpassad för den perifera synvinkeln. Vi fann att många periferasynfunktioner förbättras av optisk korrektion, särskilt för personer med centralt synfältsbortfall. Vi hittade även förbättringar i periferkontrastkänslighet för låga ortsfrekvenser när objektet modulerades med hastigheter mellan 5 och 10 Hz, vilket gäller både normalseende och personer med centralt synfältsbortfall. I periferin är det lättare att se linjer som är orienterade parallellt med synfältsmeridianen. Vi har visat att denna riktningsbias gäller både för upplösning och detektion i periferin, även när de asymmetriska optiska felen minimeras. För bästa mätnoggrannhet rekommenderar vi därför att använda randmönster som ligger snett relativt synfältsmeridianen. Denna riktningsbias skulle även kunna påverka hur den perifera bildkvalitén inverkar på utvecklingen av närsynthet. Ytterligare ett bevis för att perifer syn kan påverka den centrala synfunktionen är att, när objektets utbredning ökades, uppfattade personen det som mindre suddigt. / <p>QC 20160826</p>

No / Physiological studies of colour vision have not yet resolved the controversial issue of how chromatic opponency is constructed at a neuronal level. Two competing theories, the cone-selective hypothesis and the random-wiring hypothesis, are currently equivocal to the architecture of the primate retina. In central vision, both schemes are capable of producing colour opponency due to the fact that receptive field centres receive input from a single bipolar cell ¿ the so called `private line arrangement¿. However, in peripheral vision this single-cone input to the receptive field centre is lost, so that any random cone connectivity would result in a predictable reduction in the quality of colour vision. Behavioural studies thus far have indeed suggested a selective loss of chromatic sensitivity in peripheral vision. We investigated chromatic sensitivity as a function of eccentricity for the cardinal chromatic (L/M and S/(L + M)) and achromatic (L + M) pathways, adopting stimulus size as the critical variable. Results show that performance can be equated across the visual field simply by a change of scale (size). In other words, there exists no qualitative loss of chromatic sensitivity across the visual field. Critically, however, the quantitative nature of size dependency for each of the cardinal chromatic and achromatic mechanisms is very specific, reinforcing their independence in terms of anatomy and genetics. Our data provide clear evidence for a physiological model of primate colour vision that retains chromatic quality in peripheral vision, thus supporting the cone-selective hypothesis.

The eye is our window to the world. Human vision has therefore been extensively studied over the years. However, in-depth studies are often either limited to our central visual field, or, when extended to the periphery, only correct optical errors related to a narrow spectrum of light. This thesis extends the current knowledge by considering the full visible spectrum over a wide visual field. A broad spectrum means that the wavelength dependence of light propagation inside the eye has to be considered; the optics of the eye will therefore not form a retinal image in the same location for all wavelengths, a phenomenon called chromatic aberration. We present here a new methodology to objectively measure the magnitude of transverse chromatic aberration (TCA) across the visual field of the human eye, and show that the ocular TCA increases linearly with off-axis angle (about 0.21 arcmin per degree for the spectral range from 543 nm to 842 nm). Moreover, we have implemented adaptive psychophysical methods to quantify the impact of TCA on central and peripheral vision. We have found that inducing additional TCA degrades peripheral grating detection acuity more than foveal resolution acuity (more than 0.05 logMAR per arcmin of induced TCA peripherally compared to 0.03 logMAR/arcmin foveally). As stimuli to evaluate peripheral vision, we recommend gratings that are obliquely-oriented relative to the visual field meridian. The results of this thesis have clinical relevance for improving peripheral vision and are equally important for retinal imaging techniques. To limit the negative impacts of TCA on vision, inducing additional TCA should be avoided when the peripheral refractive errors are to be corrected, such as for people suffering from macular degeneration and central visual field loss. In retinal imaging applications, TCA leads to lateral offsets when imaging is performed in more than one wavelength. Consequently, the measurement of TCA together with careful pupil alignment and subsequent compensation can improve the functionality of these instruments. / Ögat är vårt fönster mot världen, och syn har mätts och studerats i stor utsträckning över åren. Trots detta är forskningen om mänsklig syn oftast begränsad till det centrala synfältet, och i studier av det perifera synfältet korrigeras optiska fel endast över ett smalt våglängdsområde. Denna avhandling vidgar forskningen om vår syn till att inkludera hela det synliga spektrumet över ett stort synfält. Ett brett spektrum innebär att vi måste ta hänsyn till våglängdsberoendet i ljusets brytning i ögat; ögats optik kan därför inte avbilda ett objekt till samma bildläge på näthinnan för alla våglängder, ett fenomen som kallas kromatisk aberration. Vi presenterar här en ny metod för att mäta mängden transversell kromatisk aberration (TCA) över ögats synfält och visar att ögats TCA ökar linjärt med vinkeln ut i synfältet (ungefär 0,21 bågminuter per grad från 543 nm till 842 nm). Dessutom har vi implementerat adaptiva psykofysiska mätmetoder för att kvantifiera effekten av TCA på central och perifer syn. Våra resultat visar att extra inducerad TCA påverkar den perifera förmågan att upptäcka sinusformade randmönster mer än den centrala förmågan att upplösa motsvarande ränder (mer än 0,05 logMAR per bågminut inducerad TCA i periferin jämfört med 0,03 logMAR/bågminut centralt). Vid utvärdering av perifer syn rekommenderar vi att använda sinusformade randmönster med en sned riktning jämfört med synfältsmeridianen. Resultaten som presenteras i avhandlingen har klinisk betydelse för att förbättra den perifera synen och är även viktiga för tekniker som avbildar ögats näthinna. För att begränsa den negativa effekt TCA har på synen ska man undvika att inducera extra TCA, t.e.x. när ögats perifera refraktiva fel korrigeras med glasögon för människor med makula degeneration och centralt synfältsbortfall. Vid avbildning av näthinnan ger ögats TCA förskjutningar mellan bilder i olika våglängder. Därför kan mätningar av TCA, tillsammans med välkontrollerad linjering av pupillens position och efterföljande kompensation, förbättra funktionen hos dessa instrument. / <p>QC 20160511</p>

La dégénérescence maculaire liée à l'âge (DMLA) touche actuellement un million de Canadiens, ce qui en fait la principale cause de perte de vision au Canada. La DMLA cause l’apparition d’une tache aveugle au niveau de la macula – la zone centrale de la vision. Cette tache aveugle affecte la vision centrale rendant les perceptions visuelles floues ou déformées. L’impact de cette condition est considérable puisqu’elle rend impossible la conduite, difficile la lecture et entraîne ultimement une cécité totale. La DMLA a également été identifiée comme facteur de risque de la dépression et de l’isolement sociale, ce qui porte d’autant plus atteinte à la qualité de vie des patients. Une des avenues de réadaptation pour les patients est d’améliorer leur utilisation de leur fonction visuelle résiduelle, notamment la vision périphérique. Le but de la présente recherche est d’investiguer le potentiel réadaptatif d’un entraînement imposant l’utilisation de la vision périphérique chez des participants en bonne santé en présence d’une perte de vision centrale simulée. Une compréhension des changements dans les comportements des mouvements oculaires en présence d'un scotome artificiel central aidera à développer des programmes de réadaptation pour les personnes atteint de DMLA et plus largement les personnes présentant une perte visuelle centrale. Les résultats démontrent une adaptation des stratégies visuelles des participants, entraînant une augmentation de la performance, une réduction des temps de réponse et une meilleure discrimination, suggérant ainsi que l’entraînement est susceptible de contribuer à la réadaptation des personnes atteintes de pertes visuelles centrales. / Age Macular Degeneration (AMD) currently affects one million Canadians, making it the leading cause of vision loss in Canada. AMD causes the appearance of a blind spot on the macula – the central area of vision. This blind spot affects the central vision making visual perceptions blurry or distorted. The impact of this condition is considerable since it impedes driving as well as reading and ultimately leads to total blindness. AMD has also been shown to be a risk factor for depression and social isolation, further compromising quality of life for patients. One of the avenues of rehabilitation for patients is to improve their use of their residual visual function, in particular their peripheral vision. The purpose of the present research is to investigate the rehabilitative potential of training requiring the use of peripheral vision in healthy participants in the presence of a simulated central vision loss. An understanding of changes in eye movement patterns in the presence of a central artificial scotoma will help develop rehabilitation protocols for people with AMD and more broadly people with central visual loss. Results demonstrate an adaptation of visual strategies among participants, resulting in increased performance, reduced response times and better discrimination, suggesting that training is likely to contribute to the rehabilitation of people with central vision loss.

Decline in both visual acuity and visual performance is a fact of life for older people and their increasing share of the population requires that buildings be designed with their visual needs in mind. As their field of vision decreases, people find it harder to identify an objects location, distance, and orientation. Elderly people with vision impairments usually find it harder to perform daily activities such as navigation through indoor spaces. Functional vision can be improved by modifying the design of spaces, for example, with better lighting. However, architects typically do not know how to take the needs of the visually impaired into account in their design process, or simply do not think of doing so. The researcher designed and feasibility-tested a prototype person-centered tool to help architects judge how appropriate a designed space will be for visually impaired people. The study was conducted as a qualitative mixed-methodology research analysis. The researcher used knowledge from literature interpretation to rationalize the development of a person-centered prototype. The researcher immersed design PhD students and vision science experts to inform the prototyping process. Along with an expert group of design and vision science professionals, the researcher beta-tested the prototype during a mock design-process scenario. The researcher also selected a small group of industry experts to participate in open-ended interviews on post-use demonstrations to qualitatively triangulate the findings on the prototypes usability. The study summarizes the feasibility including the challenges of using the prototype for professional purposes and suggests improvement. / Ph. D.