Vision 3

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36 Terms

1
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What are 3 features of the retinotopic map within V1?

  • inverted

  • horizontally flipped (right VF in LH)

  • distorted (cortical magnification)

2
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What is cortical magnification?

there are more cells representing the fovea than the visual periphery

3
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Why does fovea take up only 1% of retina but 50% of V1?

  • only cones which have higher visual acuity as not many to one so good detail at the fovea

  • at fovea only photoreceptors minimises bluriness so again higher visual acuity

  • all good for evolution

4
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Who mapped out the retina, focusing on peaks and declines of photoreceptors distribution in retina?

Curcio et al (1990)

5
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How many layers are in the striate cortex (V1)?

6

6
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Where do most inputs from the thalamus go to?

layers IV and V

7
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What happens in other layers?

  • higher processing in layers 2/3

  • outputs mostly from layers 2/3 corticortical

  • ouputs also from layers 5/6 subcortical

8
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Whats one attribute V1 neurons show?

orientation tuning

9
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Who investigated orientation tuning and how?

Hubel and Wiesel (1959)

  • microelectrode recordings in cat V1 while presenting bars of light against dark background

  • cells in V1 layer IV show orientation selectivity respond most strongly to bars in a particular direction

  • most be located in particular location within neurons spatial receptive field to elecit response (simple cells)

10
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How is simple cell orientation tuning computed?

  • combining four centrre/surround fields produces an orientated bar receptive field in V1 simple cells

11
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What is the difference in complex cells orientation tuning?

  • they will respond to orientation anywhere when presented within neurons spatial receptive field

  • no inhibitory surround - don’t have to be presented in middle of receptive field

12
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What else are complex cells attuned for?

motion direction selectivity

13
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How is orientation tuning organised within V1? (take sulcus and drive electrode perpendicular through)

  • cells throughout cortical layers prefer the same orientation

  • clusters of cells show similar preferred orientations in a ‘pinwheel’ arrangement across the cortical surface

14
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Do cells in V1 have occular dominance?

yes - most cells respond more robustly to inputs from one particular eye

15
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How is eye preference arranged?

into occular dominance columns across the V1 surface and throughout the cortical layers

16
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How do you investigate ocular dominance?

  • inject retina with marker

  • taken upoptic tract

  • lands in V1

  • can do in one eye or other

  • track where in visual cortex you’re getting input from each eye

17
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What’s another thing that cells in V1 are attuned to?

colour contrast

18
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How can we see colour contrast in those cells?

  • some colour sensitive cells show circular receptive fields with centre excited by one colour and inhibited by the other

  • in surround the pattern is reversed

19
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Where might we find colour double opponent cells?

  • in blobs

    • cytochrome oxidase staining in V1 shows ‘blobs’ of staining in layers 2/3

    • blobs get heavy input directly from the colour sensitive k-cells in LGN

20
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What is a V1 hypercolumn?

a local region of V1 that may contain all the possible tuning information associated with one region of the visual receptive field

<p>a local region of V1 that may contain all the possible tuning information associated with one region of the visual receptive field</p>
21
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What is the extrastriate cortex?

the part of the visual cortex located next to the striate cortex involved in processing specific features of visual information

(higher areas may inegrate sensory/motor etc)

22
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What are V2 neurons more responsive to?

  • illusory contours, binocular disparity, figure/ground responses, patterns

  • more complex receptive fields than V1

23
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What are V4 neurons responsive to?

colour, orientation, spatial frequency, figure/ground, shapes

24
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What can damage to V4 lead to?

lack of volour vision - achromatopsia

25
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What are responses in V4 strongly modualted by?

attention and show long-term plasticity - change firing through learning process

26
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What is the FFA specialised for?

  • responding to faces

  • also perhaps to visual images for which individual is an ‘expert’

    • Gauthier et al (2000) — cars and birds

  • damage leads to prospagnosia

27
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What is V5/MT specialised for?

  • visual motion perception

  • most to a particular direction

  • most not orientation or colour selective

28
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Two ways to measure V5/MT response?

  • microelectrode (extracellular) recordings

    • response of macaque MT neurons to their preferred direction is dependent on dot coherence

  • microstimulation

    • can cause monkey to think the dots are moving in their preferred direction

29
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What are the dual processing streams (Mishkin and Ungerleider, 1983)

ventral = what the object is

dorsal = where the object is

30
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What is cortical blindness?

individuals with lesions to V1 report being blind in the corresponding visual space yet can grasp objects, avoid walls etc

31
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Possible explanation for cortical blindness?

  • loss of visual awareness but not complete loss of vision

    • V1 = place of conscious perception of inputs

  • extrastriate cortex respond to images presented in cortically ‘blind’ field

  • information is reaching extrastriate visual cortex perhaps via

    • opptic tract - superior colliculus - secondary thalamus - EC

32
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What is associative agnosia?

difficulty recognising visual objects

33
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What damage causes associative agnosia?

  • brain lesions located bilaterally in occipito-temporal regions (ventral stream)

  • can copy rawingss and match obkects though so visual perception preserved, simply cannot identify

34
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What is apperceptive agnosia?

  • failure of visual perception

  • cannot identify, copy or match visual objects

  • patient DF

    • lesion to ventral

    • changed dorsal to ‘how’ stream

35
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What is akinetopsia?

  • damage in human V5 and macaque MT - motion blindness

  • dorsal stream

  • Zeki (1991) - coffee pouring

36
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What is the double dissociation?

  • dorsal lesions

    • goof visual recognition

    • poor movement vision and visual guidance of motor output

  • ventral lesions

    • opposite