Award details

Neural pathways underlying human 3D motion perception

Reference	BB/M001210/1
Principal Investigator / Supervisor	Professor Marina Bloj
Co-Investigators / Co-Supervisors
Institution	University of Bradford
Department	Faculty of Life Sciences
Funding type	Research
Value (£)	17,501
Status	Completed
Type	Research Grant
Start date	31/03/2015
End date	30/03/2018
Duration	36 months

Abstract

Anatomically, it is striking that there are multiple pathways in the visual system. Physiologically, neurons in different visual areas appear specifically sensitive to different visual information, like colour, motion or objects. Why? Dedicating different pathways to different functions can be a way of reducing the complexity of the processing problem. Here, we are interested in a specific set of pathways, those involved in the perception of motion in three dimensions. Whilst motion is known to be critical for the 'where' functions of the dorsal pathway, very little attention has been placed on how binocular information for motion is processed, nor what pathways carry out that processing. In this project we explore how specifically binocular visual information about motion-in-depth (MID) is potentially processed and carried by several different visual pathways. Two computational processes have been proposed for using binocular information for MID, and there is evidence for each of them being useful for human vision. One is the rate of change of binocular disparity over time (changing disparity, CD), the other is the binocular combination of monocular motion signals (inter-ocular velocity difference, IOVD). Both are known to be used in human vision. Our aim here is to determine if these signals processed along different fundamental pathways in the brain. We target the magnocellular (magno), parvocellular (parvo) and koniocellular (konio) pathways. The former two are well studied; disparity is carried by both pathways, motion predominantly by the magno. Of particular interest, is the fact that the konio pathway projects to extra-striate cortex without passing through V1, thus providing an alterative pathway to higher visual areas. We will use brain imaging (fMRI, EEG) and visual psychophysics, to explore where, how and why MID information may be separated across different pathways.

Summary

We use our eyes and brain to move confidently within our surroundings without bumping into things, identifying objects as dangerous or attractive and parsing subtle changes in facial expression. Vision is a hugely complex process that uses much of the brain's resources and involves a constant trade-off between energetic efficiency, speed and accuracy. How is this achieved? Clues to answer this question come from fundamental biology. Anatomically, it is striking that there are multiple pathways in the visual system and neurons in different visual areas and pathways appear differentially sensitive to certain types of visual information, such as colour or motion. It is clear that some visual brain areas and pathways have evolved at different times and for different functions. Dedicating different pathways to different functions can be a way of reducing the complexity of the processing problem - allowing the brain to compute independent properties in parallel. Here, we are interested in a specific set of pathways that seem to show strong independence of this type: those involved in the perception of motion in three dimensional space. Whilst motion is known to be critical for the 'where' functions of the dorsal pathway, very little attention has been placed on how binocular information for motion is processed, nor what pathways carry out that processing. In this project we explore how binocular visual information about motion-in-depth (MID) is processed and carried by several different visual pathways. Two computational processes have been proposed for using binocular information for MID, and there is evidence for each of them being useful for human vision. Are these signals processed along different fundamental pathways in the brain? Why is it interesting to ask this question? (1) Because neither pathway is fully understood: the sites and natures of the computations involved in processing MID in two ways have not been identified. Even more intriguingly, while one pathway, has been much studied, the other is barely explored, very poorly understood and potentially ancient, in an evolutionary sense. (2) The two pathways might perform different functions, and we propose a series of studies to specifically explore what those functions might be. Our project has very broad scope, we explore the nature of the putative pathways at the anatomical level, using functional magnetic resonance imaging (fMRI) to localize function, and source-imaged electroencephalography (EEG), which can be used to understand the temporal dynamics of visual processing. We will use psychophysical behavioural studies to study what computational processes take place during MID perception, using both a normal population to explore normal function, and a clinical group of subjects (strabismic amblyopes) that we know have compromised MID processing using one specific pathway. Additionally using Transcranial Magnetic Stimulation (TMS) to degrade information in a particular visual area we will test the causal relevance of MID-responsive regions identified with fMRI and EEG. Finally, we will also employ eye-tracking methods to understand what specific sources of MID information are useful for. Using all these techniques will allow us to get a full picture of the processes underlying MID. To achieve this we require the expertise of three institutions, and we will need to host two RA's, one with visual behavioural and eye tracking skills, the other with imaging credentials. The work proposed in this project is primarily core visual neuroscience. However, it has implications for human health. One of our techniques will exploit the fact that a person with a squint (strabismic amblyopes) is unable to use a core source of MID information, namely binocular disparity. There are hints that this group may be able to use other sources of MID. Our group will be the first to explore this issue comprehensively.

Impact Summary

Specific Users / Stakeholders Our proposal is for core human neuroscience research with no immediate application to UK-plc. However, we have identified two groups of possible indirect stakeholders, and two groups of direct stakeholders: (1) Technologists and display developers, using stereoscopic displays and stereoscopic content producers. (2) Medical professions involved in diagnosing and understanding binocular vision deficits. (3) The general public: both consumers and producers of new stereoscopic content. (4) Project researchers, who will be trained in interdisciplinary skills and exchange subject-specific knowledge. Plans for engagement (1) Technologists developing 3D material Whilst the basic neuroscientific knowledge we generate will not be of direct interest to this group, they should be interested in the our characterisation of the utility of CD and IOVD information, in other words, how important these two sources of information are for 3D display. Harris or RA1 will attend the international conference "Stereoscopic Displays and Applications", set up by IEEE, towards the end of the project to disseminate our results in the appropriate way for this audience. (2) Medical professionals Our work should be of relevance to medical professionals interested in amblyopia and strabismus, conditions that are linked and thought to be due to deficits in the development of binocular vision. One of our experiments will test a population of strabismic observers. For our purposes, we use that population's differently developed vision to test hypotheses, however, our experimental results will have relevance to the understanding of the conditions, and for their potential treatment. Towards the end of the project, we plan to invite our clinical contacts to a workshop session organised under the auspices of the Bradford Institute for Health Research to discuss the clinical implications of our work. (3) The general public We intend to make full use of the Press Relations Offices at each of the Institutions involved to maximise our outreach. To this end both RA's will attend the BBSRC Media Training Course. Wade hosts public engagement websites to teach the public about colour vision, http://www.vischeck.com/ and infant visual development http://www.tinyeyes.com/ . We will build on this experience to develop a website to demonstrate the two forms of binocular motion in depth systems that can be isolated both and allow users to generate stimuli that contain mixtures of each cue for educational purposes. Binocular vision is also a very popular topic with the general public of all ages, due in part to the recent resurgence of 3D film. This therefore provides an excellent opportunity for public engagement, to involve people in understanding how the brain is needed for sight and how 3D technology works. We have experience and equipment to deliver public displays at Science Fairs on how the psychology and neuroscience of binocular vision link to optics and ophthalmology. We plan to attend opens days and science fairs in Scotland and Yorkshire. (4) Project researchers The proposal is an interdisciplinary collaboration. We will appoint experienced postdoctoral researchers in St. Andrews and York. Each individual will experience training and will be exposed to research across disciplines, allowing us to deliver genuine inter-disciplinary scientists to the UK research community, at the end of the project. This aim will be achieved via our regular (12 in total) face to face meetings between all members of the project group.

Committee	Research Committee A (Animal disease, health and welfare)
Research Topics	Neuroscience and Behaviour
Research Priority	X – Research Priority information not available
Research Initiative	X - not in an Initiative
Funding Scheme	X – not Funded via a specific Funding Scheme

Associated awards:

BB/M001660/1 Neural pathways underlying human 3D motion perception

BB/M002543/1 Neural pathways underlying human 3D motion perception

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