Visual Cortex Flashcards

1
Q

Where do Ganglion fibres leave the retina?

A

along the optic nerve – each ganglion cell has a nerve fibre that come together to form the optic nerve

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2
Q

Where does the Optic nerve leave the eye from?

A

The blind sport

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3
Q

What is the optic chiasm?

A

– cross over point – some of the left eye and right eye fibres cross over (not all of them)

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4
Q

Beyond the optic chiasm what does the optic nerve become?

A

The optic tract

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5
Q

How is information separated in the optic tract?

A
  • Information now separated by visual field rather than by eye
  • Left and right optic nerve carry information about left and right side of the world
  • In optic tract information about right side of world crosses over to the left and vice versa:
  • Information from right visual field represented by left hemisphere and vice versa
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6
Q

What is the Lateral Geniculate Nucleus (LGN)?

A
  • The optic tract feeds into LGN
  • LGN = bilateral structure (one in left hemisphere and one in right)
  • Each LGN receives input from left and right eyes but keeps these inputs separate
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7
Q

What are the LGN receptive fields?

A
  • LGN cells have the same receptive field organisation as retinal ganglion cells: centre-surround antagonism
  • Ideal for detecting spots of light and edges
  • But not able to detect orientation
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8
Q

What is the V1?

A

the primary visual cortex in the occipital lobe

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9
Q

Where does the V1 receive it’s input from?

A

the LGN

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10
Q

What is retinotopic mapping in V1?

A

Objects close together in the visual scene are analysed by neighbouring parts of V1

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11
Q

What is cortical magnification in the V1?

A
  • Amount of cortex devoted to representing each part of the retinal field is distorted
  • Fovea represented by large area of cortex – explains why we have such good acuity when an image falls on the fovea
  • Periphery is represented by a much smaller area of cortex
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12
Q

How does single cell recording take place in V1?

A
  • Animal presented with stimuli
  • An electrode, inserted into a V1 neuron measures electrical activity
  • Activity is that of a single neuron
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13
Q

What is the V1 cell response and how was this discovered?

A
  • V1 cells have a level of baseline activity when no stimulus is presented
  • In 1950s, Hubel and Wiesel could not find a stimulus to excite the V1 cell (tried presenting lots of spots of light on the retina but didn’t work)
  • Until they found they got a big response when the edge of the glass slide moves across the receptive field: realised V1 cells will only respond to lines instead of spots
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14
Q

What are the three different types of cells in V1?

A

 Simple cells
 Complex cells
 Hypercomplex cells

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15
Q

Give features of simple cell receptive fields

A
  • Simple cells respond to oriented bars and edges
  • The receptive field has excitatory and inhibitory regions, but they are elongated
  • A vertical bar covers only the excitatory region causing a big excitatory response
  • A bar tilted slightly away from vertical, covers some of the excitatory region but also some inhibitory region causing a weaker excitatory response
  • A horizontal bar only covers a small part of the excitatory region but a larger part of the inhibitory region causing an inhibitory response
  • We say simple cells have orientation selectivity – this differs from ganglion cells
  • Orientation tuning
  • Orientation tuned neurons respond best to their preferred orientation but also respond to other similar orientations – this is what created the orientation response curve
  • Some simple cells have On-centre RFs and some have Off-centre RFs, but all have a preferred orientation
  • edge detectors and bar detectors
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16
Q

What are edge detectors?

A

simple cells with only one excitatory and one inhibitory region

17
Q

What are bar detectors?

A

Cells with 3 regions

18
Q

How are simple cells different from ganglion cells?

A

They have orientation selectivity

19
Q

Give features of Complex cell receptive fields

A
  • Respond to oriented lines but no discrete On and OFF regions
  • It will always give an excitatory response to a vertical bar of light no matter where it falls on the cell
  • Respond to moving oriented bars and edges
  • Respond best to a particular direction of movement
20
Q

Give features of hypercomplex cell receptive fields

A
  • Also called End-stopped cells
  • Respond to bars of:
     Particular orientation And
     Moving in a particular direction AND
     Particular length
21
Q

How do the receptive fields increase in complexity as we move through visual processing?

A
  • Ganglion cells respond as long as there are some kinds of light and dark
  • Simple cells only respond if it is a line
  • Complex cells only respond if it is a line moving in a particular orientation and direction
  • Hypercomplex cells only respond to a line of a particular orientation, direction and length
22
Q

How many visual areas are there beyond V1?

A

Over 30

23
Q

What are areas V3, V4 and V5 specialised in?

A
  • V3 - form of objects
  • V4 - colour information in stimulus
  • V5 - motion information in stimulus
24
Q

Is there separation of function in the visual cortex?

A

No - all areas are interconnected

25
Q

What are the two processing streams in the ventral cortex?

A

What (ventral) and Where (dorsal)

26
Q

What is the Ventral (what) stream?

A
  • Travels ventrally to inferotemporal cortex

- Important for recognising and discriminating objects

27
Q

What is the Dorsal (where) stream?

A
  • Travels dorsally to posterior parietal cortex
  • Important for determining where an object is and how to act upon it
  • Sometimes referred to as the ‘How’ stream
28
Q

What is the monkey lesion study?

A
  • Task 1: object discrimination. Food is always under the triangular prism
  • Task 2: Landmark discrimination. Food is always close to the cylinder
  • Lesion to inferotemporal cortex (what pathway) causes problems for object discrimination task but not landmark discrimination task
  • Lesion to posterior parietal cortex (where pathway) causes problems for landmark discrimination task but not object discrimination task
29
Q

What was Milner and Goodale’s experiment on patient DF with damage to his ventral pathway?

A
  • Presented oriented slot to patient DF and asked patient to match the orientation of the block they were holding to the slot
  • Patient DF couldn’t do this – controls could
  • Milner and Goodale changed it so that DF needed to post the block through the hole – now he could do it
  • Shows that there are two different processing mechanisms responsible for the two different paths – suggesting in the dorsal pathway the ‘where’ stream is still intact
30
Q

How does Optic ataxia provide evidence to the two difference processing streams?

A
  • Optic ataxia
  • Damage to dorsal pathway (‘where/how’ stream):
  • Cannot reach to grasp objects, but can recognise and describe them
  • Opposite deficits to those shown patients with visual form agnosia