anatomy/physiology of binocular vision goals –follow the m and p pathway out of primary visual...
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Anatomy/Physiology of Binocular Vision
• Goals– Follow the M and P pathway out of primary
visual cortex – Answer where binocularly and disparity
driven cells appear– Learn a bit about stereopsis – Answer (partially) how an oculocentric
neuronal organization gives rise to an egocentric visual perception
Parallel Pathways: Magnocellular (M) and
Parvocellular (P)
• Each pathway is sensitive to specific visual stimuli
• Each pathway has its own timing characteristics
• Each pathway is NOT strictly parallel!– More of a “Bob ‘N Weave” pathway
arrangement
Magnocellular (M-pathway) The Table Setter
• Coarse visual form
• Moving (or modulating)target
• Processing time: rapid
• Peripheral fusion
• Coarse stereopsis
Parvocellular (P-pathway) The Details
• Spatial detail
• Chromatic detail
• Stationary (or moving slowly) target
• Processing time: slow
• Fine stereopsis
Parallel Pathways On the Move
• Lateral geniculate nucleus• Segregation of P and M pathways into layers
(1-2 Magno.; 3-6 Parvo.)• LGN serves as a relay station to primary visual
cortex (18)– Where vision will become a conscious event
– Where stereopsis and fusion takes place
– Where visual and cognitive processing take place
Primary Visual Cortex (V1)
• Located along calcarine sulcus• M and P pathways continue in different
paths as they reach layer 4 of V1
– M pathway to layer 4 C– P pathway to layer 4C and layer 4A
• Organized into ocular dominance zones– Monocular cells in layer 4C– Binocular driven cells outside of layer 4C
Parallel Pathways in V1
• M pathway:
– From 4C to layer 4B in same vertical column (1 mm wide)
– From 4B to layers 2/3 in same vertical column (1 mm wide)and neighboring columns
Parallel Pathways in V1
• P pathway:
– From 4C to layers 4A and 3 in same vertical column (1 mm wide)
– In layer 3, cytochrome oxidase, a metabolic marker, has dense staining in layer 2/3; absent in layer 4
– Called “blobs”– Although considered “P-cells only”, a significant
M-pathway input exists
Parallel Pathways in V1
• Blob and interblob regions:a split in the parvocellular pathway
• Blob regions are situated in the center of ocular dominance columns– Blob regions: color opponency, low contrast and
spatial frequency, not orientation selective– Interblob regions: little color opponency, high
contrast and spatial frequency, very orientation selective
M and P Pathways In V2
• V2 has areas of high cytochrome oxidase activity in form of thick and thin stripes
• M pathways project to thick stripes
• P pathway– Blob cells: thin stripes– Interblob cells: inter
stripes
Other Visual Areas • V2: in area 18, flanking V1
– Thin/inter stripe regions (P pathway) projects to V4
– Thick stripe (M pathway) projects to V3 and MT
– Some overlap in response characteristics in V2 due to “cross-talk” between M and P at blob region
Other Visual Areas• V3: in area 18 flanking V2
– Receives M pathway input– Output to middle temporal
area (MT)– Also output to V4!?!
• V4
– Receives P-pathway input from thin/inter stripe regions of V2
– Receives strong M-input
Vision Association Areas
• Area MT– In parietal lobe– M-pathway input– Output to parietal areas
and V4– Sensitive to motion– Some areas have
receptive fields in head-centric coordinates, NOT oculocentric
Vision Association Areas• Inferotemporal
cortex
• P-input (V4): fine stereopsis, color vision, fine pattern vision
• Complex object recognition: faces
• Posterior parietal cortex
• M-input (MT/V4): coarse stereopsis, low spatial freq., fast flicker and motion
• Spatial position and object motion
Final Words About M/P Pathways
• Significant cross-talk in V1, V4 and beyond
• Ultimately, these two independent, yet overlapping streams must converge to form unitary perceptions of objects
• We do not process the world like a poorly printed photograph, with the colors offset
Ocular Dominance Columns
• Vertical columns that respond most strongly to one eye
• Extends through the full thickness of V1
• Absent in areas outside V1
• Binocular cells outside layer 4C respond predominantly to one eye over the other
Orientation Columns
• If ocular dominance columns are loaves of bread, orientation selective columns are slices (parallel to pia)
• Orientation selectivity is interrupted by blobs
Binocular Cells and Stereopsis
• Binocular cells in V1 receptive fields for each eye share most characteristics– Corresponding
retinal loci
– Latency
– Size/shape of receptive field
• If perfect overlap of receptive fields exist, it argues for a creation of an EGOCENTRIC PERCEPTION early in visual processing
• It cannot explain, however, why we are sensitive to binocular disparity (stereopsis)
• Binocular cells in V1 receptive fields for each eye share most characteristics– Corresponding
retinal loci
– Latency
– Size/shape of receptive field
Binocular Cells and Stereopsis
Binocular Disparity
• Results from different perspective of each eye to a particular visual target
• Neurons tuned to disparity have been found in V1
• Receptive fields for each eye do not PERFECTLY overlap
• More prevalent in V2 (75% cells tuned to disparity)
• 4 main classifications of disparity tuned cells– Near cells/ Far cells– Excitatory cells tuned to
zero disparity– Tuned excitatory– Tuned inhibitory
Profiles of Disparity Tuned Cells
• Near cells: resp. to targets closer than fixation distance
• Far cells: resp. to targets farther than fixation distance
• Excitatory cells tuned to zero disparity: narrow peak responses around zero disparity
Profiles of Disparity Tuned Cells
• Tuned excitatory: stim. by stimuli near zero disparity BUT ON EITHER SIDE/ suppressed by uncorrelated images
• Tuned inhibitory: suppressed by stimuli near zero disparity BUT ON EITHER SIDE / stim. by uncorrelated images