Transcript Lecture S&P
Chapter 6
The Visual System
From Your Eyes to Your Cortex
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What do we see?
Somehow a distorted and upsidedown 2D retinal image is transformed
into the 3D world we perceive
2 types of research needed to study
vision
Research
probing the components of the
visual system
Research assessing what we see
Light Enters the Eye and Reaches
the Retina
No species can see in the dark, but some
are capable of seeing when there is little
light
Light
Photons
of energy
Waves of electromagnetic radiation
Humans see light between 380-750
nanometers
The Conversion of Light to Neural
Signals
–conversion of one
form of energy to another
Visual transduction – light energy to
neural signals by visual receptors
Pigments absorb light
Absorption spectrum determines
spectral sensitivity
Transduction
The retina-geniculate-striate
pathway
~90% of axons of retinal ganglion cells
Information from the left visual field of
each eye projects to the right lateral
geniculate nucleus (LGN) and vice versa
Most LGN neurons that project to primary
visual cortex (V1, striate cortex) terminate
in the lower part of cortical layer IV
Retinotopic organization
Information received at adjacent portions
of the retina remains adjacent
More cortex is devoted to areas of high
acuity – like the disproportionate
representation of sensitive body parts in
somatosensory cortex
About 25% of primary visual cortex is
dedicated to input from the fovea
Lateral Inhibition and Contrast
Enhancement
Visual
system detects change
Mach bands – nonexistent stripes
that visual system creates to enhance
the contrast and make edges easier
to see – an example of contrast
enhancement
A consequence of lateral inhibition
Receptive Fields of Visual Neurons
The
area of the visual field within
which it is possible for a visual
stimulus to influence the firing of a
given neuron
Hubel and Wiesel looked at receptive
fields in cat retinal ganglion, LGN,
and lower layer IV of striate cortex
Receptive Fields of Visual Neurons
Similarities
Receptive
seen at all 3 levels:
fields of foveal areas smaller
than those in the periphery
Circular receptive fields
Monocular
Many had a center-surround
organization
Receptive Fields in Striate Cortex
Neurons of lower layer IV are an exception
– circular receptive fields (as in retinal
ganglion cells and LGN)
Most neurons in V1 are either
– receptive fields are rectangular with
“on” and “off” regions
Complex – also rectangular, larger receptive
fields, respond best to a particular stimulus
anywhere in its receptive field
Simple
Receptive Fields in Striate Cortex
SIMPLE
Rectangular
“on” and “off” regions,
like cells in layer IV
Orientation and
location sensitive
All are monocular
COMPLEX
Rectangular
Larger receptive fields
Do not have static
“on” and “off” regions
Not location sensitive
Motion sensitive
Many are binocular
Columnar Organization of V1
Cells with simpler receptive fields send
information on to cells with more complex
receptive fields
Functional vertical columns exist such that all
cells in a column have the same receptive field
and ocular dominance
Ocular dominance columns – as you move
horizontally, the dominance of the columns
changes
Retinotopic organization is maintained
Seeing Color – 2 Theories
Trichromatic
theory (component
theory)
Proposed by Young, refined by
Helmholtz
3 types of receptors, each with a
different spectral sensitivity
Seeing Color – 2 Theories
Opponent-process
theory
Hering
2
different classes of cells encoding
color, and another class encoding
brightness
Each encodes two complementary
color perceptions
Seeing Color – 2 Theories
are correct – coding of color by
cones seems to operate on a purely
component basis, opponent
processing of color is seen at all
subsequent levels
Both
Color Constancy and the Retinex
Theory
Color constancy – color perception is not
altered by varying reflected wavelenths
Retinex theory – color is determined by
the proportion of light of different
wavelengths that a surface reflects
Relative wavelengths are constant, so
perception is constant