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Vision Sensation
Retina: light → photoreceptor cell → bipolar cell → RGC →
→ Forebrain: thalamus → cerebral cortex V1
we understand vision in the retina because the activity there is solely determined by what the animal sees
transition from sensation to perception occurs in V1
Visual Thalamus
our understanding becomes more limited as soon as we get to the visual thalamus (4th cell in the circuit) because only 10% of the inputs to the visual thalamus come from the retina
other inputs come from other areas of the brain, and the info encoded in those pathways is unknown
Lateral Geniculate Nucleus (LGN)
a nucleus in the thalamus
many RGCs project here and then LGN neurons project to the visual cortex
left visual field goes to the right hemisphere
right visual field goes to the left hemisphere
each hemisphere gets input from both eyes
Superior Colliculus
involved in controlling fast reflexive movements in response to light
Hypothlamus
regulates sleep/wake cycles
Receptive Field
a description of the physical stimulus that activates a neuron
area of visual space (relative to a fixation point) where light is capable of changing the activity of a neuron
to identify receptive field, we train an animal to stare at the centre of a screen, and then systematically shine some pattern of light in different areas of their visual space
Horizontal Cell
type of retinal cell
accentuate contrast by boosting NT release from photoreceptor cells that are more dimly lit than their neighbours
regulates adjacent photoreceptor and bipolar cells
do not have action potentials
release glutamate in a graded manner dependent on their membrane potential
Receptive Field of Photoreceptor Cell
leaky sodium ions are open in the dark and are already depolarized
release more glutamate in the dark than the light
location of visual space where it detects light (relative to the fixation point)
wavelength of light its most sensitive to
Bipolar Cells
there are ON and OFF bipolar cells
specialize in detecting small increases and small decreases in light intensity, respectively
no action potentials
graded glutamate release dependent on membrane potential
ON Bipolar Cells
most sensitive to increases in brightness
express inhibitory metabotropic glutamate receptors
activity patterns are the opposite of the photoreceptor cells that connect to them
inhibited by glutamate
in the light:
depolarize and release glutamate
photoreceptor cells: sodium channels close → hyperpolarized, and release less glutamate
ON bipolar cells are less inhibited → so depolarizes
In the dark:
hyperpolarize and stop releasing glutamate
photoreceptor cells: sodium channels open → depolarized, release more glutamate
OFF Bipolar Cells
most sensitive to decreases in brightness
express normal excitatory ionotropic glutamate receptors
activity patterns follow the photoreceptor cells connected to them
excited by glutamate
in the light:
hyperpolarize and do not release glutamate
photoreceptor cells: sodium channels close → hyperpolarized, release less glutamate
in the dark:
depolarize and continuously release glutamate
photoreceptor cells: sodium channels open → depolarized, release more glutamate
Bipolar Cell Receptive Fields
horizontal cells create a “centre-surrounded” organization in the receptive fields of bipolar cells
sum of the receptive fields of the photoreceptor cells that connect to it
characterized by:
location in visual space (relative to fixation point)
wavelength of light it is most sensitive to (centre of its receptive field)
whether the light in the centre of its receptive field causes ON or OFF response
in the fovea:
bipolar cells receive input from only one photoreceptor cell, so the centre of its receptive field is the same size as one photoreceptor cell (high resolution vision)
outside the fovea:
bipolar cells receive input from many photoreceptor cells, so the centre of their receptive field is the size of many photoreceptor cells’ receptive fields summed together (low resolution vision)
Amacrine Cells
detect motion and movement direction by integrating info from neighbouring bipolar cells
regulate the excitability of adjacent bipolar and ganglion cells
don’t report absolute light levels
only signal when there are changes in light across time
release NT onto several cell types (RGCs, bipolar cell terminals, and other amacrine cells)
RGCs
express excitatory glutamate receptors
activity mostly follows the bipolar cells that connect to them
also have a “centre-surrounded” organization and are classified as ON and OFF for light and colour
ON RGCs
increase their rate of spiking when light is in the centre of their receptive field
decrease their rate of spiking when light is only in the surround area
OFF RGCs
opposite of ON RGCs
decrease their rate of spiking when the light is in the centre of the receptive field
increase their rate of spiking when light is only in the surround area
RGCs in the Fovea
process colour by integrating inputs from many bipolar cells
A “Yellow On” center indicates the RGC is processing information from at least two cone cells in the center position
(one red and one green, via ON bipolar cells, that have overlapping receptive fields).
A “Blue Off” surround indicates that it is also processing information from several blue cone cells (via OFF bipolar cells) that surround the red/green cone cells.
Receptive Field of Thalamic Neurons
similar to that of RGCs
Receptive Field of Neurons in V1
sum of many thalamic LGN neurons
simple cells in V1 are sensitive to lines of light
their receptive fields are typically organized in centre-surrounded fashion
Primary Visual Cortex
also known as V1 and striate cortex
Neurons in V1 spike when there is a line of light in a particular orientation in their receptive field.
some V1 neurons respond best to vertical lines, some to horizontal, and some to lines oriented somewhere in between
V1 neurons have a larger receptive field and respond to various orientations of light
does this by all neurons in one cortical column analyzing the same pixel of visual space
this helps identify borders, edges, and corners
neurons downstream of V1 put this info together to identify whole objects and their position in space
Extrasiate Cortex
synonymous with visual association cortex
areas V2, V3, V4, V5, etc.
Where Pathway (dorsal)
dorsal stream to parietal lobe
involved in identifying motion and spatial relationships
encodes:
whether anything is moving in visual space (V5)
how can I move to interact or avoid the object
What Pathway (ventral)
ventral stream to temporal lobe
involved in identifying shapes and colours
encodes:
what objects are there
what colour are the objects (V4)
sensation:
retina - light detection
→ V1 - edge detection (lines and orientation)
perception:
→ V2 - shape detection (two lines form an angle; two angles create a shape)
→ early ventral visual stream - object identification (independent of viewing angle)
→ late ventral visual stream - object identification (this is a banana)
meaning:
→ semantic interpretation - this is something i can eat
Monocular Vision
some V1 neurons respond to visual input from just one eye
depth perception
Binocular Vision
most V1 neurons respond to visual input from both eyes
each provide a different perspective to the same area of visual space
depth perception
Depth Perception
there are many monocular cues that can be used to estimate depth, such as relative size, amount of detail, relative movement as we move our eyes etc.
we use these cues to perceive depth when looking at a 2D image, only one eye is required for monocular cues
Stereopsis
perception of depth that emerges from the fusion of two slightly different projections of an image on the two retinas
difference between the images from the two eyes is called retinal disparity
results from the horizontal separation of the two eyes
improves the precision of depth perception, especially for moving objects, and is helpful when playing sports or when pouring a glass of water
Visual Agnosia
V1 works, but part of their visual association cortex is damaged
agnosia is a deficit (problem) in perception – a deficit in the ability to recognize or comprehend certain sensory information (like visual detection of objects, colors, and motion), even though sensation of the sensory information is not defective.
people with an agnosia generally have intact memories and knowledge of the sensory features that they can no longer perceive (through a particular sensory modality)
Akinetopsia
disability in movement perception
damage in the dorsal stream (V5)
people describe seeing the world as a series of snapshots
Cerebral Chromatopsia
denying colour perception
damage to ventral visual stream (V4)
people describe things as looking dull or drab
shades of gray
V4 is involved in both perception and memory of colour
Predictive Coding Theory
every level of visual processing is affected by predictions of what’s interpreted at lower levels and a feedback error signal to correct future predictions