Cognitive And Clinical Neuropsychology Of Vision (Year 3) Flashcards

1
Q

Define sensory transduction

A

Conversion of one energy form to another e.g light energy into electrical energy

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2
Q

Briefly outline some arguments for vision being an indirect process

A
  1. Sensory transduction: Light has to be processed into electrical energy, and then processed again to form visual images
  2. Inversion/reflection: Crossover of information from left/right top/bottom (info in the right/left visual fields are projected to the opposite cerebral hemisphere)
  3. Cortical magnification - PVC gets most of its info from the fovea, however this info is magnified (fovea is disproportionately represented in early visual areas but we do not see the world that way
  4. We can perceive illusions - visual experience goes beyond the sensory input
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3
Q

Give some characteristics of vision

A
  1. Innate
  2. Indirect
  3. Influenced by context
  4. Actively reconstructed
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4
Q

Define an ischemic stroke

A

Strokes caused by a blockage/blood clot

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5
Q

Give three parallel pathways in vision

A

Magno, parvo and koniocellular pathways

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6
Q

Where does information cross over?

A

The optic chiasm

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7
Q

Explain how Visual information crosses over at the optic chiasm

A

Left visual fields from both eyes-> right side of brain
Right visual fields from both eyes -> left side of brain

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8
Q

Describe the role of the cornea

A
  • Focuses light onto the retina
  • Fixed
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9
Q

Describe the role of the pupil

A

-The aperture in the iris
- Changes size according to light levels

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10
Q

Describe the role of the lens

A
  • Focuses light
  • Adjustable (accommodates light levels)
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11
Q

Describe the role of the retina

A
  • Rods and cones in retina absorb light and convert it into electrical signals
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12
Q

Describe the path of a signal from the optic nerve to the rods and cones

A
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13
Q

Give the number of rods and cones per eye

A

125 million rods per eye
6 million cones per eye

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14
Q

Give the number of nerve fibres per eye

A

800,000 per eye

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15
Q

Explain the function of nerve fibres

A

Pool signals from multiple rod or cone receptors

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16
Q

Describe the function of rods

A
  • Achromatic night vision
  • 1 Type
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17
Q

Describe the function of cones

A
  • Daytime, achromatic and chromatic vision
  • 3 types
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18
Q

Give the three types of cones

A
  • Long-wavelength sensitive (red cone)
  • Middle-wavelength sensitive (green cone)
  • Short wavelength sensitive (blue cone)
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19
Q

Give the wavelength of visible light

A

350-700nm

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20
Q

Describe the role of wavelength sensitive cones in the retina

A
  • Short, middle and long wavelength sensitive cones are sensitive to a different range of wavelengths
  • L and M are strongly overlapping, s is sensitive to bluish light
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21
Q

define mesopic range

A

Rods and cones

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22
Q

Define phototopic range

A

Cones only

23
Q

Give the maximum and minimum pupil

A

maximum: 7.9mm
minimum: 2.0mm

24
Q

Describe the function of the fovea

A
  • High acuity area - outputs from only a few cone cells are pooled together
  • Cones are used in normal lighting conditions and provide us with high acuity and colour vision. We move our eyes to bring important things onto the fovea.
25
Describe the distribution of rods and cones
Rods are mostly in the periphery, outside the fovea - rods only function under low light conditions
26
Explain why there is low acuity in the periphery
Outputs from hundreds of rod cells are pooled together
27
Explain what the blind spot is and why we don't see a black spot
Where the optic nerve leaves the retina so no rod or cone cells to detect light Brain 'fills in the gap'
28
Where does parallel processing start?
in the retina
29
Give the three types of retinal ganglion cells and what wavelengths they process
Midget - red-green Parasol - light-dark Bistratified - yellowish-purple
30
Give the properties of Midget ganglion cells
70-80% incidence rate Photopic luminance only Spatial response: opponent Spectral response: L vs M (central) L + M (peripheral) Temporal response: sustained Projection - Parvo LGN
31
Give the properties of parasol ganglion cells
8-10% incidence Phototopic/scotopic Spatial response: opponent Spectral response: L+M Temporal response: Transient Projection: Magno LGN
32
Give the properties of bistratifired ganglion cells
Below 10% incidence Photopic only Spatial response: nonopponent Spectral response: S vs (L+M) Projection: Konio LGN
33
Describe the structure of the lateral geniculate nucleus
layered structure layer 1,4,6 input from contralateral eye layer 2,3,5 input from ipsilateral eye Layers 1,2: Magnocellular (from Parasol cells) Layers 3,4,5,6: parvocellular layers (from Midget cells) ventral to each layer, numerous tiny neurons are found, the koniocellular layers (Konio, greek: dust; input from Bistratifed cells) Retinotopic map – topographically arranged receptive fields
34
Describe the different functions of the P,M,K layers in the LGN
• P,M,K layers have different functions M cells: large receptive fields, larger cell bodies, respond to transient information P cells: small cell bodies, sustained response K cells: very small cell bodies; implicated in colour vision
35
Describe the structure of the primary visual cortex
Primary visual cortex: anatomically distinct layers (1-6) Layer 4 divided into 4 sublayers (4A,4B,4Calpha, 4Cbeta) Parvo, magno, and konio divisions of the LGN project selectively into different layers. Most of the input goes to Layer 4C: LGN magnocellular layers project to 4C alpha LGN parvocellular layers project to 4Cbeta Konio cells project to superficial layers 2 and 3 Information is kept separate in visual cortex!
36
Describe the structure and function of parvo and magnocellular pathways
- ‘luminance/achromatic/light-dark pathway’ and ‘red-green’ pathways have bee extensively characterised - Majority of photoceptors feed into the P and M pathway and subserve most visual functions: spatial vision including high acuity vision; motion vision; form perception - Function of koniocellular pathway is not fully understood; phylogenetically the oldest pathway
37
Describe the function of the Koniocellular pathways
Koniocellular pathway gets input from the nonP, nonM retinal ganglion cells and is probably involved colour perception
38
Describe the function differ ences between the parvo and magnocellular pathways
- Response to contrast - Different sensitivity to spatial frequencies 1. Different spectral tuning: Parvo: ‘L-M’; Magno:’ L+M’ Parvocellular neurones: respond best to red-green modulations Magnocellular neurones: respond best to achromatic modulations 2. M and P neurones have different contrast gains 3. Different sensitivity to different spatial frequencies (SF)
39
Describe how gratings in different colour directions can be used to isolate the different pathways
40
Describe how we see colours
An image of the world is projected by the cornea and lens onto the rear surface of the eye: the retina. The back of the retina is carpeted by a layer of light- sensitive photoreceptors (rods and cones).
41
Describe the role of photopigments
The rods all have the same photopigment, rhodopsin. But there are three different types of cones in the human retina, each with a slightly different photopigment. (L, M,S cones) The 3 photopigments absorb and reflect different wavelengths of light, giving rise to the different colors in the picture.
42
Describe how human cone mosaics
The three different types of cones are arranged randomly in the retina (shown as red, green, and blue in this in the picture). These are the retinas of two different subjects (AN and JW). It is remarkable how different the number and the distribution of the L and M cones are. Yet, these differences in the retinal make-up do not result in different colour experiences.
43
Define trichromacy
Trichromacy: colour is encoded by the relative outputs of the three cone classes
44
Explain colour-opponent theory
Hering was the first to notice that some pairs of colours, namely red and green, and yellow and blue, cannot be perceived at the same time. He named these pairs of colours the opponent colours (red-green, yellow-blue) since they are mutually exclusive colours. The perceptual ‘red-green’ colour direction is not aligned with the LGN L-M direction. The perceptual yellow-blue colour direction is not aligned with the LGN S-(L+M) direction. Therefore, the colour signals are transformed again somewhere in visual cortex (or beyond) to provide us with the percept of ‘red’, ‘green’, ‘yellow’, ‘blue’ etc.
45
Describe early chromatic pathways in LGN
Three cone classes supply three "channels" The achromatic channel receives nonspectrually opponent input from L- and M cone classes The two chromatic channels receive spectrally opponent inputs to create the L-M or red-green channel and S-(L and M) or blue yellow channel
46
Explain our perceptual representation of colour
Perceptual representation of colour: Hue is what we could loosely refer to as colour, as in red, yellow, blue etc. Hueless or achromatic colours include black, gray, white. Saturation refers to purity, or how much grey there is in a colour. Brightness goes from complete dark to white.
47
Explain why physically different lights can look identical to us
Just three cone receptors underlie colour vision
48
Describe the evolutionary advantage of seperate L and M cones
Most mammals are dichromats (short and medium- or long- wave). Primates because of the advantages of detecting red/orange fruit against a green background, evolved a third pigment (L and M)
49
Describe the two kinds of colour deficits
1. Congenital (Retinal) (one or more of the three kinds of cones is missing) Protanopia: L cones are missing Deuteranopia: M cones are missing Tritanopia: S cones are missing 2. Cerebral: the damage is to the cortex, often in the extrastriate area V4 (Zeki, 1973). Cerebral Achromatopsia Cerebral Hemiachromatopsia
50
Describe how colour deficiencies are diagnosed
Ishihara plates Farnsworth-Munsell D-15 test
51
Give the location of the striate visual cortex and extra striate visual cortex
V1 - SVC V2, V3, V4, etc - EVC
52
Desccribe Lueck et al, findings
Hypothesis: Neurones in colour-selective brain areas will respond more vigorously to the chromatic Mondrian compared to the achromatic (black-white) one. Neural activity is obtained by measuring cerebral blood flow. Expected colour-selective area: V4 (‘colour area’) Change in CBF in different brain areas: Changes in responses a coloured Mondrian are shown in black; Changes in response to a black-white Mondrian are shown in grey. Striate cortex (V1) responds well to both colour & achromatic stimuli V2 also showed similar activation, but resolution was not high enough to reliablu distinguish V2 from V1. ‘Colourarea’ (V4): responds more to colour than achromatic stimuli ~ 12-14% A small increase in the Temporo-occipto- parietal area (V5) ~3-5%
53
Desccribe Cowey and Heywood's findings
Damage aroud fusiform gyrus associated with only partial achromatopsia