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Oxyopias Archive 1999

Basic, clinical, or applied vision topics hosted by the UCB School of Optometry.

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Oxyopias Schedule


Wednesday, December 8th, noon in room 489 Minor Hall

Ian G. Cox
Research Fellow at Research Clinic Bausch & Lomb, Rochester, NY
Host: Ken Polse

The effect of lens material and design features on lens movement - in-vitro and in-vivo investigations

Abstract

The role of lens material and design features in on-eye lens movement has historically been driven by clinical observation using commercially available lens products. Unfortunately this invariably leads to a number of uncontrolled lens material and design variables that confound the clinical results and lead to erroneous hypotheses. This lecture describes a series of controlled clinical studies to determine the effect of lens material and design features on lens movement and centration. Attempts to confirm these findings with laboratory off-eye models, and theoretical models will also be covered.

 

December 3 , 11:am - 12:30 pm 2515 Tolman

Jitendra Malik
Computer Science, University of California at Berkeley
Co-sponsored by Institute for Cognitive Studies
Host: Steve Palmer

Computational Mechanisms Of Visual Grouping

Abstract

I shall argue that early and intermediate level processing in the visual system be modeled as a three stage process. The first stage is a measurement stage carried out in V1 with spatiotemporal receptive fields tuned to orientation, spatial frequency, opponent color, and short-range motion. The second stage is a grouping stage resulting in the formation of regions of coherent brightness, color and texture. Call these 'proto-surfaces'. The third stage results in the formation of surfaces/objects with attached properties such as lightness, object motion, occlusion relationships (figure-ground), depth, slant-tilt etc and is based on the combined operation of Gestalt grouping factors, shape cues, and can be partially influenced by knowledge of familiar configurations.

The first stage can and has been modeled by many researchers using tools of linear system analysis. We offer a novel approach to the second stage by modeling it as the process of finding a partition of the image into regions such that there is high similarity within a region and low similarity across regions. This is made precise as the 'Normalized cut' criterion which can be optimized by solving an eignevalue problem. The resulting eigenvectors provide a herarchical partitioning of the image into regions ordered according to salience. Brightness, color, texture, motion similarity, proximity and good continuation can all be encoded into this framework. We show results on complex images of natural scenes which demonstrate the significant superiority of this technique over classical approaches based on edge detection. Phenomena such as subjective contours emerge as side consequences.

Our work on the third stage is preliminary; I shall argue on computational and psychophysical grounds that modular shape processing should be abandoned, and that grouping driven by ecological statistics is as crucial as shape cues driven by ecological optics.

This talk is based on joint work with Jianbo Shi, Thomas Leung and Serge Belongie.

 

October 29, Noon, 489 Minor Hall

Laurent Itti
California Institute of Technology - Computation and Neural Systems
Pasadena, CA 91125
Host: Lawrence Stark

A Bottom-Up Search Mechanism for Over and Covert Shifts of Visual Attention

Abstract

Most models of visual search, whether involving overt eye movements or covert shifts of attention, are based on the concept of a saliency map, that is, an explicit two-dimensional map that encodes the saliency or conspicuity of objects in the visual environment. Competition among neurons in this map gives rise to a single winning location that corresponds to the next attended target. Inhibiting this location automatically allows the system to attend to the next most salient location. We describe a detailed computer implementation of such a scheme, focusing on the problem of combining information across modalities, here orientation, intensity and color information, in a purely stimulus-driven manner. The model is applied to common psychophysical stimuli as well as to a very demanding visual search task. Its successful performance is used to address the extent to which the primate visual system carries out visual search via one or more such saliency maps and how this can be tested.

 

October 22 Friday, Noon 489 Minor Hall

Michael Landy
Dept of Psychology, New York Univeristy
Host: Marty Banks

Exploring Early Vision Using Oriented Textures

Abstract

Substantial evidence indicates that early visual coding includes both 1st-order and 2nd-order mechanisms. "1st-order mechanisms" is just another name for the now-familiar, linear, spatial-frequency channels. 2nd-order mechanisms involve a 2nd-order linear filter that follows an intervening nonlinearity. We have used oriented textures (either randomly placed oriented line segments or filtered noise) to investigate these 2nd-order spatial mechanisms. Results indicate that:

  1. there is a preference for 1st- and 2nd-order filters to be orientationally aligned;
  2. some texture pairs are discriminable for which there are no built-in texture edge mechanisms;
  3. there are multiple, bandpass, spatial-frequency tuned, 2nd-order filters just as in the 1st-order case.
The third conclusions stems from a continuing series of experiments that applies the techniques used to characterize 1st-order filters (e.g., contrast sensitivity, summation, increment threshold, etc.) to the 2nd-order filters.
 

October 8 Friday, 2:00 Noon, 489 Minor Hall

Jay Enoch
School of Optometry, Group in Vision Science, UC Berkeley
Host: Cliff Schor

The first known lenses: Remarkable Egyptian lenses from ca. 4600 year

Abstract

They were parts of apparent schematic eyes in Egyptian statues. Included was a lively visual illusion where the observer seemed to be followed by the pupils of these eyes as he/she rotated about the statue. The illusion will be demonstrated in an accompanying model.

 

October 1 Friday ,12:00 noon, 489 Minor Hall

Maureen K. Powers
Visiting professor in Molecular and Cell Biology, UC Berkeley
Host: Marty Banks

What can a regenerated retina see?

Abstract

The central nervous systems of some fish and amphibians continue to add new neurons in adulthood, unlike humans, and they have the remarkable capacity to regenerate following traumatic injury, also unlike humans. The source of the normal and injury-induced neuronal addition in fish retina is a special class of stem-like cell which normally divides throughout life. Functional studies have been aimed at determining whether the new retinal cells that are formed in turn form new projections to the brain, and whether the new retina-brain complex can support vision. We find that connections to the optic tectum do return, and that the electroretinogram, optokinetic nystagmus, dorsal light response, and the ability to respond to dim lights in a classical conditioning paradigm all return as well during regeneration. The quality of vision seems generally to be correlated with the quality of retinal regeneration as assessed morphologically. However, even in the best cases visual capacity is diminished: Animals are less sensitive scotopically, have poor spatial vision and are probably deficient in color vision. Retinal disorganization, non-optimal connections and abnormal photopigment complements may be responsible for the deficits. Although imperfect, the natural retinal regeneration process in goldfish clearly does support sensory function, leading to the hope that retinas in other vertebrates (ultimately humans) might be induced to do the same.

 

September 29, Wednesday 12:00 noon, 489 Minor Hall

Bart Anderson
MIT, Dept of Brain & Cognitive Sci, Cambridge MA
Host: Cliff Schor

Synthesizing contours from moving images

Abstract

One of the fundamental problems of recovering scene geometry involves the computation of occlusion relationships. Both stereopsis and motion generate spatio-temporally unmatched image regions along occlusion boundaries, yet both domains have been dominated by computational strategies that require corresponding features to be present in the multiple views. I will describe a new class of contour synthesis mechanisms that we have discovered in the motion domain that relies on the presence of these unmatched features, a model of contour synthesis, and the relevance of these findings for statistical (Bayesian) models of scene interpretation.

 

September 24, Noon ,489 Minor Hall

Pablo Artal
Laboratorio de Optica,, Universidad de Murcia, Spain
Host: Stan Klein

Aberration Measurement And Correction In The Human Eye


Abstract

A real-time wavefront sensor for the human eye will be described. New results on the aberrations' temporal dynamics and on the relative contribution of the ocular components (cornea and lens) to the overall eye's aberrations will be presented. Strategies for correcting the ocular aberrations and their impact in vision and high resolution retinal imaging will be also discussed.

 

September 17 ,Noon , 489 Minor Hall

Lynn Marran PhD, OD
UC Berkeley, School of Opometry
Host: Cliff Schor

Aniso-Accommodation and its clinical implications?

Abstract

Aniso-accommodation is unequal accommodation of the eyes occurring simultaneously while in the binocular state. Marran and Schor(1998) demonstrated that 0.75D of aniso-accommodation could be reliably elicited in subjects. Previous (Ogle, 1937; Spencer et al 1954; Stoddard & Morgan, 1942; Ball, 1952) and recent (Flitcroft, 1992; Koh et al, 1998; Carlin et al, 1998;) investigators have had equivocal results in demonstrating aniso-accommodation. This talk will address the unique characteristics of the response and hence the conditions that are required to evoke and measure it. These characteristics both explain the equivocal results and also suggest what role aniso-accommodation may play in the non-laboratory setting. In particular, a possible role of aniso-accommodation in the induction / or recovery from anisometropia will be discussed.

 

August 27 Friday, 12:00 Noon, 489 Minor Hall

Mitesh Kapadia
Univ. Pennsylvania Neuroscience and Rockefeller University

Lateral interactions in primary visual cortex and their role in perception

 

July 27 Tuesday, 12:00 Noon, 489 Minor Hall

Jan Koenderink
Utrecht Biophysics, Fysisch Laboratory RUU, Netherlands
Host: Jitendra Malik

Pictorial Relief

Abstract

When the human observer looks at a photograph of a scene the perception is of a curious twofold nature: One sees the photograph as an object (a flat piece of paper with various pigmentation in a certain simultaneous order) and at the same time one looks into the photograph into "pictorial space." Pictorial space is three, rather than two dimensional. When the pictorial space is like the physical space of the scene at the time the photograph was taken one calls that perception veridical. Since photographs typically underdetermine the scene one expects such veridical perceptions to be rare and due to either change occurrance or prior knowledge. When it is known which major cues are used by the observer, it is possible to describe the remaining ambiguity formally. In general bilinear problems (for instance "shape from shading") this ambiguity is a shear in threespace that leaves the image plane invariant. I will show examples of nonveridical perceptions that differ by exactly these transformations but are metrically different to a surprising degree. Human observers appear to apply such ambiguity transformations in order to "move the mind's eye" in pictorial space.

 

June 25, 12:00 Noon, 489 Minor Hall

Gopathy Purushothaman
University of Houston
Host: Ralph Freeman

Oscillatory visual percepts and their putative neural mechanisms

Abstract

It has been known for over a century that visual percepts of very bright static flashes and moving objects have a repetitive nature, and have been referred to as Recurrent Images and "Charpentier's Bands," respectively (Bidwell, 1894; Charpentier, 1896; McDougall, 1904). Early explanations of these phenomena attributed these percepts to the rhythmic discharges observed in some retinogeniculocortical neurons (Frohlich, 1912; Buttneret al, 1969). The recent physiological investigations of theseoscillatory activities and their putative functional roles motivateda re-examination of these psychophysical phenomena. In a series of studies, we measured psychophysically.

  1. the impulse responses to bright stationary flashes,
  2. the perceived number of recurrences in the percept of pairs of flashes, and
  3. the Charpentier bands in the smear of bright moving targets.
Our data show significant inter-subject, inter-trial and intra-trial variabilities in several aspects of the oscillations, including their frequencies and latencies. Despite these variabilities, a computational model can be used to show that the temporal impulse response to a stationary flash can account for the perceived number of recurrences in static flashes and the patterns of the Charpentier bands.

This study suggests that neural oscillations are unlikely to constitute a robust internal code. If oscillations and/or their coordination were an ideal code, then they would be inaccessible at the perceptual level. Our study, on the other hand, shows that, under certain stimulus conditions, the putative code (oscillations) can interfere with the information that it carries (perceived quality of the stimulus).
 

May 21, 12:00 Noon, 489 Minor Hall

Andrew Parker
University Lab of Physiology, Oxford
Host: Marty Banks

Binocular Neurons and the Perception of Depth

Abstract

The first stage in the primary visual pathways at which there is significant binocular convergence lies in cortical area V1. Many neurons in V1 are highly sensitive to binocular disparity and they undoubtedly play an important intermediate role in the detection of stereoscopic depth. I will present several results from our laboratory that highlight discrepancies between the psychophysical perception of stereoscopic depth and the characteristics of these V1 neurons. These results point to an important role for extrastriate cortex in stereoscopic vision.

 

May 3 (Monday), 12:00 Noon, 489 Minor Hall

Nansi Jo Colley
Ophth and Vis Sci and Genetics, University of Wisconsin, Madison, WI
Host: Sheldon Miller

Molecular Genetics of the Drosophila Visual System

Abstract

The overall objective of our research program is to utilize Drosophila as a model for studying hereditary human diseases that cause retinal degeneration and eventual blindness. The complexity and variations of retinal degeneration disorders has lead to the identification of multiple subtypes, each with a distinct genetic and biochemical basis. This complexity, the infrequent availability of ocular tissues from patients, and the broad base of knowledge of Drosophila genetics combine to make Drosophila a powerful animal model for studying human disease. We are engaged in two areas of research. One set of projects is focused on rhodopsin trafficking in the secretory pathway and the other deals with the role of calcium in photoreceptor function. To understand mechanisms of calcium modulation, we have initiated the characterization of a novel sodium/calcium-potassium exchanger in Drosophila, NCKX30C.

Photoreceptors in both Drosophila and humans alike, utilize a photopigment, rhodopsin, for vision. During biosynthesis, rhodopsin is specifically targeted to the site of vision within the photoreceptors. One goal of our studies is to further elucidate the mechanisms of protein targeting and trafficking in the photoreceptor cells. We have previously shown that defects in rhodopsin trafficking result in severe retinal defects and retinal degeneration in Drosophila. Similar mechanisms are thought to occur in some human retinal degeneration disorders. In fact, more than twenty five percent of all autosomal dominant retinitis pigmentosa (ADRP) cases appear to be caused by mutations in the gene encoding the visual pigment rhodopsin, located on human chromosome 3q. Over sixty distinct mutations in rhodopsin have now been reported in ADRP patients. The mechanism by which the mutant rhodopsin proteins cause dominant retinal degeneration has been actively investigated in Drosophila as well as in vertebrates. In screening mutagenized Drosophila chromosomes we have recovered thirteen mutations in the gene encoding rhodopsin. All 13 mutations entail single nucleotide changes, which together define 10 different sites in the protein. Remarkably, four such missense mutations in Drosophila (G119E, P184L, E194K and G195S) correspond to mutations in exactly the same amino acid residues found in known human ADRP (G106R, P171L, E181K and G182S, respectively). We have demonstrated that in these cases, retinal degeneration results from interference of the assembly of mature wild type rhodopsin by the mutant proteins.

Intracellular free calcium influences several distinct time-dependent cellular events in human and Drosophila photoreceptors. Therefore, the precise control of spatial and temporal profiles of calcium are extremely important for photoreceptor function. In addition, the prolonged elevation of cytosolic calcium can be toxic and could lead to retinal degeneration. Cells maintain their low cytosolic calcium levels using ATP-driven pumps and sodium/calcium(-potassium) exchangers. To understand the molecular basis of calcium modulation, we are characterizing a sodium/calcium-potassium exchanger (NCKX30C) that is expressed in the Drosophila photoreceptors. Genetic screens for mutations in the Drosophila visual system continue to yield exciting phenotypes that define novel photoreceptor genes and mechanisms for photoreceptor function and retinal degeneration in vivo.

 

April 29 (Thursday), 3PM, 489 Minor Hall

Fiona Stapleton
Host: Suzi Fleiszig

Epidemiology, basic and clinical science approaches in understanding contact lens related disease

Abstract

Epidemiological studies of ocular disease provide information on their frequency, distribution and associated risk factors. This type of data can assist in the management of disease but also can initiate basic and clinical science approaches to testing specific hypotheses relating to the pathogenesis of disease.

This methodology has been used in the evaluation of the pathogenesis of contact lens related disease. Initial anecdotal reporting of lens related disease during the 1980's led to the development of large scale prospective cohort and case control studies to estimate the size of the problem and to determine specific risk factors. In certain groups of complications, risk factors such as overnight wear and the type of care system and its frequency of use were identified as associated risk factors.

The identification of overnight lens wear as a major risk factor in certain groups of complications led to the formulation of hypotheses of the impact of eye closure coupled with lens wear on ocular defense mechanisms. Consequently, increased levels of tear and serum proteins, cytokine and chemokine synthesis, complement activation, leukocyte recruitment to the ocular surface and an increase in ocular biota have all been demonstrated during uncomplicated eye closure. Lens wear adds a further dimension to ocular defense during eye closure, by affecting tear and membrane bound glycoproteins, altering leukocyte recruitment, inhibiting tear exchange, providing a vector for bacterial carriage and by providing a potentially antigenic stimulus. Hypothesis testing for each of these different factors will be discussed

Ocular surface, contact lens and bacterial interactions are complex. Understanding contact lens related complications clearly requires a multidisciplinary approach to elucidate the pathogenesis and suggest preventive strategies.

 

April 26 (Monday), 12:00 Noon, 489 Minor Hall

Lawrence O'Keefe
Center for Neuroscience, New York Univeristy
Host: Ralph Freeman

Motion Processing Mechanisms in the Primate Visual Cortex

Abstract

Our understanding of motion processing in the visual system is largely based on studies using stimuli whose motion is cued by luminance (first-order motion). However, there are many kinds of stimuli whose motion is cued not by luminance, but rather by contrast, color, or texture ("second-order" motion). Psychophysical studies suggest that first- and second-order motion information may be processed by independent mechanisms. I wish to know how this psychophysical dissociation is reflected in neural pathways -- is there is a single neural pathway mediating motion perception, or do several neural pathways each mediate a different aspect of motion perception?

My approach is to compare responses evoked by conventional first-order motion targets to those evoked by a class of second-order motion targets designed to elude detection by conventional motion mechanisms. I have used this approach in combination with psychophysical techniques in human observers, single unit recordings in areas V1 and MT of anesthetized monkeys, and more recently, single unit recordings in area MT of alert monkeys. By comparing behavioral and neuronal sensitivity to first- and second-order motion, I hope to identify and characterize neuronal populations that mediate the perception of different kinds of motion.

 

April 22 (Thursday), 3PM, 489 Minor Hall

Izumi Ozhawa
School of Optometry, University of California, Berkeley

Functional Organization of the Primary Visual Cortex and Beyond

Abstract

Hierarchical organization and parallel processing in central visual pathways are well established. However, the key roles played by specific cell types and the details of neural circuitry are still not understood. Our exploration of general receptive field characteristics of visual neurons provides clues about how cortical neurons are built and what information they carry. I will discuss my plans for investigating cortical neurons beyond the initial stages.

 

April 19 (Monday), 12:00 Noon, 489 Minor Hall

Andrew Goldberg
HHMI/Department of Biochemistry, University of Washington, Seattle, WA
Host: John Flannery

Towards an understanding of inherited retinal degenerations: disease-linked mutations in peripherin/rds and rom-1

Abstract

Towards an understanding of inherited retinal degenerations: disease-linked mutations in peripherin/rds and rom-1. The identification of heritable mutations that cause progressive retinal dystrophies holds promise for understanding and eventually treating many debilitating eye diseases. Inherited defects in the photoreceptor-specific peripherin/rds and rom-1 polypeptides result in a surprising and unprecedented heterogeneity of human retinal diseases. The variety of clinical presentations underscores the importance of peripherin/rds and rom-1 for human vision, but fails to reveal the molecular details of pathogenesis. Using purified retinal photoreceptor membranes, I have shown that peripherin/rds and rom-1 form the subunits of an integral membrane protein complex that is restricted exclusively to the rim regions of both rod and cone photoreceptor outer segment disks. This complex is proposed to play a role in outer segment disk morphogenesis and stability. I have developed a cell culture system for the heterologous expression and characterization of peripherin/rds and rom-1, and used biochemical, immunochemical and biophysical analysis to probe aspects of protein structure, function and role in human retinal diseases.

 

April 15 (Thursday), 3PM, 489 Minor Hall

Michael Berry II
Department of Molecular and Cellular Biology, Harvard University
Host: Ralph Freeman

Anticipation of Moving Stimuli the Retina

Abstract

The visual system has a delay of ~50 ms in processing flashes of light, largely arising in the retina. Such a delay poses severe problems for timing motor output with moving objects (for instance, hitting a tennis ball). Using a flat array of 61 electrodes to record action potentials from up to 80 ganglion cells at once, we have found that a moving bar elicits a traveling wave of ganglion cell activity that peaks at or even ahead of the bar's leading edge. This anticipation of moving objects mirrors a recently reported visual illusion: observers perceive a moving bar to be ahead of a flash at the same location. The measured spatial extent and temporal dynamics of a ganglion cell receptive field cannot account for motion anticipation. However, a model that includes a contrast gain control mechanism is highly successful. In some sense, anticipation is a modest form of prediction that the eye makes about the near future.

 

April 8 (Thursday), 3PM 489 Minor Hall

Frank Schaeffel
University Eye Hospital Tuebingen, Experimental Ophthalmology
Hosts: Ian Bailey & Stan Klein

The visual control of eye growth: systems analysis, optics and biochemistry


Abstract

The length of the eye is normally properly matched to the focal length of cornea and crystalline lens. However, in the industrial nations, there is a trend of eyes becoming too long and myopic. Both experiments in animal models and studies in humans suggest that visual experience has a significant impact on ocular elongation. To prevent exaggerated growth and myopia, two approaches emerge: (1) restriction of the critical visual experience and (2) reduction of the gains of the visual feedback loops that control axial eye growth by pharmacological agents. To use these approaches successfully, it has first to be clarified (1) what the critical features in the retinal image are and (2) which messengers are released from the retina to control the growth of the underlying sclera and how they can be modified. Our progress in both areas will be described. In addition, our new refraction technology will be demonstrated (the PowerRefractor). Myopia.

 

March 29, Noon, 489 Minor Hall

Christine Wildsoet
New England College of Optometry
Host: Stan Klein

Emmetropization, accommodation and myopia: what can the chick model tell us about their association?

Abstract

That extensive near work and myopia are linked is a belief held by many in relation to human myopia yet little understood in terms of causality. However, recent research using animal models has provided some insights into the issues involved. Progress on this front reflects, at least in part, the fact that stimulus conditions can be more readily manipulated and controlled. In this paper, I will present some of my more recent research using the chick as such a model.

 

March 12, 12:00 Noon, 489 Minor Hall

Benjamine Backus
Stanford University
Host: Marty Banks

Response of human visual brain areas to binocular disparity

 

March 5, 12:00 Noon, 489 Minor Hall

Joel Miller
Smith Kettelwell Eye Research Foundation
Host: Jim Maxwell

Convergence and Co-contraction

 

Jan 22, 12:00 noon, 489 Minor Hall

Michael Kubovy
Psychology Dept. at Universitiy of Virginia
Fourth Annual Irvin Rock Memorial Lecture, co-sponsored with the Institute for Cognitive Studies
Host: Steve Palmer

On Perceptual Grouping

Abstract

In this lecture I will present progress we have made on understanding two related phenomena first described close to a century ago: grouping by proximity and grouping by similarity. I will:

  1. Show how the stimuli used by Gestalt psychologists - regular dot patterns - can be generalized and how their phenomenological approach can be extended to give stable, replicable, and quantifiable data.
  2. Present a Pure Distance Law that captures the probabilistic features of grouping by proximity and a Attenuator Hypothesis that captures properties of grouping by similarity.
  3. Show how our data suggest a Theory of Grouping, a probabilistic theory in which the central construct is Attraction, which can be measured on a ratio (or even an absolute) scale.
  4. Sketch some open problems.
 
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