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optic nerve
an unmyelinated collection of axons from ganglion cells
these axons make up the blind spot in the eye
optic chiasm
the left and right optic nerves meet here to cross information
information goes from each eye to both hemispheres of the brain, and each hemisphere receives input from the contraleteral visual field
ipsilateral information and contralateral information
ipsilateral
information from the visual world that does not cross the optic chiasm and remains on the same side of the brain
goes to layers 2, 3, and 5 of each LGN
example: L temporal (out to the left) retina receives information from the R visual field and stays on the same side through the LGN
L nasal retina receives information of the R visual world as well, but this information will cross over to the L LGN
contralateral
information from the visual world that crosses the optic chiasm to go from 1 side to the other
layers 1, 4, an 6 of the LGN
example: L nasal retina receives information of the R visual world - this information crosses over to the L LGN
L temporal retina receives information from the R visual field but stays on the same side through the LGN
optic tract
contains crossed (contralateral) fibers from 1 eye and uncrossed (ipsilateral) fibers from the other eye
optic nerve from each eye splits in half here after meeting in the optic chiasm
left visual world is processed in the R hemisphere of the brain, right visual world is processed in the L hemisphere of the brain
number of fibers depends on the placement of the eyes (humans v
contralateral representation of visual space
left visual world is processed in the R hemisphere of the brain, right visual world is processed in the L hemisphere of the brain
LGN and superior colliculus
2 main pathways from the optic tract (where does visual info go after the optic tract?)
optic nerve
optic chiasm
optic tract
LGN or superior colliculus
LGN to visual cortex
list the path of the primary visual pathway
superior colliculus
the “where” system (in the primary visual pathway)
superior colliculus
located at the top of the brainstem beneath the thalamus - controls automatic saccades (rapid eye movements from 1 focal point to another) and smooth eye movements (tracking)
purposeful eye movements - positions eyes in the right place when you want to look at something
orienting head = “where”
activates multisensory cells when a visual stimulus has another (e.g., auditory) stimulus attached with it - enhancement
receives approximately 10% of information from ganglion cells/optic tract
saccades
controlled by the superior colliculus - rapid eye movement from 1 object to another
smooth eye movements
controlled by the superior colliculus - requires fixation within the foveal area to track something as it moves
example: watching a bird fly across the sky
you can’t move your eyes like this just by scanning the room or reading; eyes consistently move from 1 object to another unless focusing on something actively moving, resulting in this
LGN
the “what” system in V1
LGN
located near the thalamus - responsible for organizing and regulating information from the retina before it is sent to the cortex, and receives it back in a feedback information loop
bilateral structure with 6 layers of cells and a retinotopic map of the retina
ipsilateral information: 2, 3, 5
contralateral information: 1, 4, 6
2 types of pathways: parvo and magno
parvo: layers 3, 4, 5, and 6
magno: layers 1 and 2
functions
relay station: info flows in from different places in the brain and is sent out to different places in the brain
edge detection: light/dark, edges/boundaries
reticular activating system: sleep/wake cycles
organizes info: which eye info comes from, color vs noncolor, movement, form information
receives feedback from visual cortex
magno (magnocellular)
pathway of the LGN
large cells that fire in bursts when triggered
rods AND cones
responsible for movement and flickers/light detection
larger receptive fields that are sensitive to light but not color
movement, light detection
what the magno pathway of the LGN is responsible for
parvo (parvocellular)
pathway of the LGN
small cells (midget retinal ganglion cells) with a sustained firing pattern when triggered
cones - fovea
responsible for color, fine texture pattern, depth - visual acuity
layers 3, 4, 5, and 6 of the LGN
color, fine texture pattern, depth, visual acuity
what the parvo pathway of the LGN is responsible for
3, 4, 5, 6
layers (#) of the LGN dedicated to the parvocellular pathway
1 and 2
layers (#) of LGN dedicated to magnocellular pathway
parvo and magno (parvocellular and magnocellular)
2 pathways of the LGN
ipsilateral: 2, 3, 5
contralateral: 1, 4, 6
LGN cell layer organization
retinotopic organization
point by point topography of the retina
preserves information about where in the world infomation comes from and which eye each image comes from
keeps spatial structure - cells next to each other process things that are next to each other in areas next to each other
LGN and V1
LGN and V1
the 2 structures in the visual pathway with retinotopic organization
bilateral
a structure that is this has 1 in both hemispheres of the brain
LGN and V1
LGN and V1
the 2 bilateral structures in the visual pathway
striate cortex, V1
names for the primary visual cortex
V1
primary visual cortext in the occipital lobe - info comes in from the LGN to here
essential for all higher perception and cognition, contianing approximately 250 million cells
bilateral structure
left hemisphere receives visual info from the R visual world, and the right hemisphere receives visual info from the L visual world
meets in center to represent the fovea
organization
retinotopic organization/representation of the retina
cortical magnification
6 layers - LGN (parvo/magno) connections with some layers of the cortex
simple cells, complex cells, hypercomplex cells
retinotopic, cortical magnification
organization of V1
cortical magnification
in V1 - in which the cortex increases processing for a specific area/information
more space in the cortex is dedicated to some sensory receptors than others
something in the fovea is not fully magnified by the cortex, but receives more cortical area than the periphery
convergence to divergence
in which visual information condenses from rods and cones (~100 million cells) to ganglion cells (~1 million cells) and disperses amongst the striate cortex (~250 million cells)
Hubel and Weisel
researchers responsible for discovering visual cortex and the preferences of different cells in V1
simple, complex, hypercomplex
simple, complex, hypercomplex
the 3 types of neurons in the striate cortex that respond best to/prefer specific types of edge information shown to the eye
simple cells
in V1 - type of neuron with excitatory and inhibatory areas arranged side-by-side that respond best to edges/lines of a certain orientation
static
position selectivity: specific area of a visual field
orientation selectivity: certain orientation
color selectivity - dark against light OR light against dark
complex cells
in V1 - type of neuron that likes moving edges, lines, and bars in any area of the visual field
can like dark against light AND light against dark
direction selectivity
hypercomplex cells
in V1 - type of neuron that likes moving curved lines/bars
size selectivity
in reference to V1 neurons - responds best to things of a certain size
similar to ganglions with smaller/larger receptive fields
orientation selectivity
in reference to V1 neurons - simple cells respond best to lines/bars of a certain fixed orientation
position selectivity
V1 neurons - simple cells prefer stimuli to be in a specific area within the visual field
physical placement matters for peak response
not an issue in complex cells
color selectivity
in reference to V1 neurons - simple cells prefer different color combos (either/or)
complex cells will respond to both
direction selectivity
in V1 neurons - complex cells like when information is moving in a specific direction
size, orientation, position, color
selectivity of simple cells in V1
direction
selectivity of complex cells in V1
dorsal and ventral
2 streams for processing visual info in the extrastriate cortex (beyond V1)
lesion studies
dorsal
pathway in extrastriate cortex that processes “where” information
in parietal lobe (responsible for attention and somatosensory system)
magno layers of the LGN - movement
parietal - attention and somatosensory system
what lobe is the dorsal pathway in? what is it responsible for?
ventral
pathway in extrastriate cortex that processes “what” information
in temporal lobe (memory, language, and auditory system)
parvo layers of the LGN - visual acuity, color, texture, to perceive and recognize objects
temporal - memory, language, auditory system
what lobe is the ventral pathway in? what is it responsible for?
parvo
layers (pathway) of the LGN that the ventral pathway in extrastriate cortex is connected to
magno
layers (pathway) of the LGN that the dorsal pathway in extrastriate cortex is connected to
monkey lesion studies
study that led to the discovery of the dorsal/ventral pathways, in which severing each one resulted in an inability to either find an object (dorsal) or remember what an object is (ventral)
functional modularity
different parts of the brain function with different responsibilities in the cortex
visual agnosia
in which a person cannot recognize a visual stimulus (2D or 3D) just by looking at it
they don’t know what it is due to brain damage, not within the eye itself
prosopagnosia
inability to recognize faces
object agnosia
type of visual agnosia in which a person cannot recognize physical (3D) objects, not just visual stimulus
achromatopsia
inability to recognize color (not the same as colorblindness, which happens in the cones)
seeing things in B/W/G
visual agnosia, prosopagnosia, object agnosia, achromatopsia
types of issues that arise when there is damage to the different parts of the visual cortex
relay station, edge detection, reticular activation system, organizes info, receives feedback from visual cortex
LGN functions