Grant: Discovery Grants Program - Individual
Dalhousie University
$50,000.00
Plasticity of development of vision and of the mammalian central visual pathways
FY 2014-15
Summary
The major objective of my research program is to understand how the development of the pathways in the brain that process vision, and hence vision itself, are influenced by what an animal sees early in its life. From studies on animal species such as monkeys and kittens that have visual systems organized for accurate binocular depth perception (stereoscopic vision) like that of humans, it is known that there are so called ""critical periods"" in development during which abnormal or biased visual input can have a permanent effect on the development of the visual pathways which in turn result in visual impairments. The altered development of the visual pathways induced by an episode of abnormal early visual input is now thought to underlie the common (~3% of the population) developmental visual disorder called amblyopia (""lazy eye""), that is defined as poor vision that does not originate in the eye itself. The experiments I conduct explore the origins of this disorder through studies of how certain forms of abnormal input influence the vision of cats including their ability to perceive motion, to follow moving objects with their head and eyes and to strike at them with one of their paws. The majority of the experiments involve evaluations of the vision of the kittens by use of visual displays and tasks similar to those used to test the vision of amblyopic humans. A central theme of the experiments is the idea that not all visual input is treated equally during development; brief periods of normal binocular input where the two eyes see the same thing simultaneously, are weighted preferentially to prevent the development of amblyopia even when most visual input is grossly abnormal. I will examine whether the critical amount of binocular input is determined by the proportion of input that is normal or by an absolute amount of such input. In addition, I will examine whether division of the abnormal input into separate episodes will weaken its effectiveness.
Program
Discovery Grants Program - Individual
Recipient
Location
Nova Scotia, Canada
Recipient Type
Academia
Type
Grant
Source
NSERC's Awards Data
As published
Application id
7660-2010
Name nom
Mitchell, Donald
Department département
Psychology
Organization id
79
Institution établissement
Dalhousie University
Province en
Nova Scotia
Province fr
Nouvelle-Écosse
Country en
CANADA
Country fr
CANADA
Fiscal year exercice financier
2014
Competition year année de concours
2010
Award amount
50000
Program id
RGPIN
Program name en
Discovery Grants Program - Individual
Program name fr
Programme de subventions à la découverte - individuelles
Group en
Discovery grants programs
Group fr
Programmes de subventions à la découverte
Committee code
1502
Committee name en
Biological Systems and Functions
Committee name fr
Systèmes et fonctions biologiques
Area of application code
1101
Area of application group en
Health, education and social services
Area of application group fr
Santé publique, éducation et services sociaux
Area of application en
Human health (including medically-related psychological research)
Area of application fr
Santé publique (y compris recherche psychologique liée à la médecine)
Research subject code
6400
Research subject group en
Life sciences research related to human health and disease
Research subject group fr
Sciences de la vie liées à la santé publique et aux maladies humaines
Research subject en
Life sciences research related to human health and disease
Research subject fr
Sciences de la vie liées à la santé publique et aux maladies humaines
Partie
5
Nb partie
5
Application title
Plasticity of development of vision and of the mammalian central visual pathways
Keyword
NSERC
Application summary
The major objective of my research program is to understand how the development of the pathways in the brain that process vision, and hence vision itself, are influenced by what an animal sees early in its life. From studies on animal species such as monkeys and kittens that have visual systems organized for accurate binocular depth perception (stereoscopic vision) like that of humans, it is known that there are so called ""critical periods"" in development during which abnormal or biased visual input can have a permanent effect on the development of the visual pathways which in turn result in visual impairments. The altered development of the visual pathways induced by an episode of abnormal early visual input is now thought to underlie the common (~3% of the population) developmental visual disorder called amblyopia (""lazy eye""), that is defined as poor vision that does not originate in the eye itself. The experiments I conduct explore the origins of this disorder through studies of how certain forms of abnormal input influence the vision of cats including their ability to perceive motion, to follow moving objects with their head and eyes and to strike at them with one of their paws. The majority of the experiments involve evaluations of the vision of the kittens by use of visual displays and tasks similar to those used to test the vision of amblyopic humans. A central theme of the experiments is the idea that not all visual input is treated equally during development; brief periods of normal binocular input where the two eyes see the same thing simultaneously, are weighted preferentially to prevent the development of amblyopia even when most visual input is grossly abnormal. I will examine whether the critical amount of binocular input is determined by the proportion of input that is normal or by an absolute amount of such input. In addition, I will examine whether division of the abnormal input into separate episodes will weaken its effectiveness.