Lecture 1 and 2 - Colour vision Flashcards

1
Q

What are the peak wavelength sensitivities of long, middle and short wavelength cones?

A

long - 560nm
middle - 530nm
short - 430nm

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2
Q

opsins are expressed in the…

A

outer cone segments and are bound to a chromophore

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3
Q

Spectral sensitivities of cones are determined by…

A

Opsins

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4
Q

Complete the sentence:
Small changes in the____________ __ _______ _______ that make up opsins can significantly shift the peak of the absorption spectrum

A

sequence of amino acids

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5
Q

Where are the genes that encode the L- and M- cones opsins found?

A

on the X chromosome at Xq28

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6
Q

Where are the genes that encode the S-cone opsins found?

A

on chromosome 7 (7q32)

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7
Q

The colour appearance of an object depends on:

A

1) The colour properties of the light source

2) The absorption/reflection properties of the object

3) The colour processing of the eye and brain

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8
Q

Rushton’s Principle of Univariance states that:

A

The effect of any photon of light absorbed by a photopigment is independent of its wavelength

(therefore lights of different spectral distributions will therefore appear identical if they produce the same absorptions in the three photopigments)

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9
Q

What are the three colour processing pathways

A

1) Luminance pathway where L and M cones are combined (L+M) (Black and white)

2) Red-Green pathway where L and M cones are subtracted (L-M)

3) Blue-Yellow pathway (S-(L+M))

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10
Q

The combination of cone signals (luminance, red-green and blue-yellow) takes place where

A

within the retina via different neural circuits leading to the 3 distinct pathways known as magno-, parvo-, konio-cellular pathways

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11
Q

Cone opponent pathways from retina to
cortex:

Magnocellular pathway

A
  • Carries luminance/achromatic information
  • Diffuse Bipolar Cells receive input from L + M cones
  • Diffuse Bipolars then connect with Parasol Ganglion Cells, the axonal fibres of which transmit information to the lateral geniculate nucleus (LGN)
  • and then input to layers 4Ca
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12
Q

Cone opponent pathways from retina to
cortex:

Parvocellular Pathway

A
  • red-green chromatic information from the L and M cones in the fovea
  • is transmitted via Midget Bipolar Cells ,
  • The midget bipolars then connect with Midget Ganglion Cells the axons of which constitute the first section of the Parvocellular pathway
  • input to layer 4Cβ
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13
Q

Cone opponent pathways from retina to
cortex:

Koniocellular Pathway

A
  • S-cones has its own functional pathway whereby signals from the S-cones are fed via S-cone bipolar cells to bi-stratified ganglion cells
  • combined inhibitory inputs from L+M are fed to ganglion cells via diffuse bipolars with horizontal cells providing necessary lateral interactions in this circuit.
  • Bi-stratified ganglion cell signals are carried to the cytochrome oxidase blobs in layer 2/3 in V1
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14
Q

colour information is sent from V1 to

A

V2 which consists of 26 -34 parallel, pale, dark thick and dark thin cytochrome oxidase staining stripes perpendicular to V1.

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15
Q

Most of the neurons in the thin stripes are

A

selective for chromatic stimuli, double opponent and have connections with V4

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16
Q

Extra-striate area V4 forms the next important area in the colour pathway receiving the majority of inputs from V1, V2 (thin and inter-stripe regions) and sends projections to the…

A

infero-temporal cortex (IT)

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17
Q

what is the pre- frontal cortex important for?

A
  • important in decision making and has strong
    reciprocal connections with the anterior inferior temporal (IT) cortex, the final stage of the colour
    pathway.
18
Q

What is the Munsell system

A
  • objective method of measuring and specifying colours
  • contains over 1200 colour samples
  • each Munsell colour is described by three variables: hue, value and chroma
19
Q

How is colour represented in the Munsell colour system?

A
  • Hue (dominant wavelength) is defined by different points around a circle.
  • The value (lightness scale) is represented vertically.
    -The chroma scale (which is equivalent to the amount of colour or saturation) is represented radially emanating out from the centre of the circle.
  • Minimally saturated (low chroma) colours are towards the centre, highly saturated colours (high chroma) radially further outwards
20
Q

What is the CIE system of colour specification?

A
  • international standards organisation for the
    measurement of colours and lights.
  • Measurements in this system are based upon trichromatic colour matching characteristics of a standard ‘normal’ observer
  • a test light of a certain colour is presented in one half of a bi-partite field and can be matched by a mixture of different amounts of three primary lights (red, green & blue) in the other half of the field.
  • When a colour match is made the two halves of the field have different spectral radiation content but appear identical.
21
Q

What are tristimulus values

A
  • Three values that together are used to describe a colour and are the amounts of three reference colours that can be mixed to give the same visual sensation as the colour considered. Symbol: X, Y, Z. See also chromaticity coordinates.
22
Q

How can we calculate chromaticity coordinates using X,Y and Z tristimulus values

A

x=X/X+Y+Z
y=Y/X+Y+Z
z=Z/X+Y+Z

X+Y+Z=1

23
Q

what is normal colour vision known as

A

trichromatic colour vision

24
Q

what is monochromacy

A
  • when there is a single photoreceptor
  • monochromats are totally colour blind
  • they see changes in colour as changes in brightness
25
Q

What is Dichromacy

A
  • Two photoreceptors
  • better colour vision that monochromats but still limited
  • colour can be detected as long as the 2 cone types produce different responses to different wavelengths
26
Q

what are colours which are physically different but appear the same called

A

metamers

27
Q

What are the L, M and S cone opsin genes known as

A

L-cone opsin genes - OPN1LW
M-cone opsin genes - OPN1MW
S-cone opsin genes - OPN1SW

28
Q

What is the percentage similarity between nucleotide sequences of L,M & S cones

A

L and M - 98% identical nucleotide sequence
they are only 40% similar to S-cone gene

29
Q

How many exons do L and M cone opsin genes have and what is the most important one.

A
  • 6 exons (functional regions of genes that code specific proteins)
  • Exon 5 is most important as it encodes the amino acids that are responsible for the main spectral sensitivity differences between the L-and M-cone opsin
30
Q

What is usually the first gene (upstream gene) in individuals with normal colour vision

A

The fist gene (most upstream) in the array always encodes an L pigment in individuals with normal colour vision

31
Q

What controls whether the L or M genes gene is switched on

A
  • A section of DNA on the X chromosome known as the locus control region (LCR).
  • it is located upstream of the L and M cone opsin genes and dictates which of the two genes is expressed.
32
Q

what is tetrachromacy

A
  • referred to as super colour vision
  • refers to the possibility that some females may have four cones
  • This is due to the fact that OPN1LW and OPN1MW are on the X chromosome and females who are heterozygous (i.e have two different versions of the same gene)
    could potentially have two different forms (the longer and shorter peak sensitivity variants)
  • 2 L cone variants, 1 M cone and 1 S cone
33
Q

what are the prefixes given to defects characterized by the absence of L-, M- and S- cones

A

L-cones defects: protan-
M-cone defects: deutan-
S-cone defects: tritan-

34
Q

what percentage of men do protan and deuatan defects commonly affect

A

8% to 10% of men in the USA

tritan defects are rare: 1 in 10,000 people

35
Q

what is the most severe red-green colour deficiency

A

The dichromacies

36
Q

what pigments have deuteranopes and protanopes lost

A

deuteranopes- lost their M pigment
protanopes- lost their L pigment

37
Q

The milder forms of red-green colour deficiency are…

A

the anomalous trichromacies

38
Q

what are the two kinds of anomalous trichromacies

A

protanomaly and deuteranomaly

39
Q

Protanomalous trichromats are missing…

A
  • the normal L cone pigment, just like the protanopes.
    -However, they do have a form of trichromatic colour vision (as the name implies), but their trichromacy is not based upon normal L, M and S pigments. Instead they have an S cone pigment and 2 M (or M-like) pigments that have a small difference in their spectral peaks
40
Q

Deuteranomalous trichromacy

A
  • based upon 3 cone photopigments, an S cone plus 2 spectral subtypes of L cones .
  • As a basis for 2 spectral types of L pigments, all those individuals with deuteranomaly have at least 2 different genes to encode the L opsins
41
Q

what does the spectral proximity hypothesis propose?

A
  • proposes that colour discrimination ability depends upon the size of the difference between the absorption spectra of the pigments
  • the bigger the differences in the spectral peaks of these two photopigments, this would improve colour vision further
42
Q

what are the four basic types of colour vision tests?

A

1) pseudoisochromatic plates - Ishihara and hardy rand rittler
2) hue discrimination tests - Farnsworth D15, Fransworth-munsell 100 hue test, city university test
3) Anomaloscopes - Nagel
4) lantern tests - Holmes-wright