Sensory system: Vision Flashcards

1
Q

What does it mean to say that vision is based on interrelationship?

A

Just like in a melody, we recognize not the sequence of notes, but there interrelationship.

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2
Q

What is meant by a ‘winner-take-all’ perceptual strategy?

A

only one part of the image can be selected as the focus of attention

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3
Q

Why is vision called as a creative process?

A

Gestalt psychology: What we see represents the organization of sensations by the brain.
Max Wertheimer: The brain makes certain assumptions about what is to be seen in the world, expectations that seem to derive in part from experience and in part from the built-in neural wiring for vision.

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4
Q

What are the assumptions about the visual objects?

A

1) We fill in what is not there
2) Muller-Lyer illusion: We judge the size from the shape
3) Object recognition: Filling in the missing details

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5
Q

How is the size of an object perceived?

A

The size depends on other objects in the visual field.

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6
Q

What is meant by occlusion?

A

Making sense of the patterns

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7
Q

What are rods and cones?

A

Rods: sensitive to light, low spatial resolution, slow recovery of current, many rods connect to one bipolar cell
•Cones: very high spatial resolution (visual acuity) and not sensitive to light; mediate color, have a sharp response, one-to-one connection to bipolar cells.

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8
Q

What are the simillarities of rods and cones?

A
  • contain photoreceptors (activated by light)
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9
Q

What are the differences of rods and cones?

A
  • size and shape
  • range of luminance: rods more sensitive than cones
  • fovea: distribution of cones and rods
  • connections to bipolar cells (Cones are responsible for visual acuity: one-to-one connection to bipolar cells. But many rods on one bipolar cell)
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10
Q

How does phototransduction of dark current work?

A

In the absence of light, cation channels in rods and cones are kept open by intracellular cGMP and conduct an inward current, carried largely by Na+.

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11
Q

What are the principal steps of phototransduction?

A

(1) Light is absorbed by and activates pigment molecules (opsin or rhodopsin in rods)
(2) The activated pigment stimulates a G protein (transducin), which in turn activates cGMP phosphodiesterase. This enzyme catalyzes the breakdown of cGMP to 5-GMP.
(3) As the cGMP concentration is lowered, the cGMP-gated channels close, reducing the inward current and causing the photoreceptor to hyperpolarize.

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12
Q

How do rods and cones respond to light?

A

by graded hyperpolarizing response

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13
Q

How is color vision established?

A

3 kinds of cone opsins sensitive to different light wavelengths

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14
Q

When are you color blinded? (dichromacy)

A

red-green color blindness due to the absence of either M or L cones

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15
Q

Name the aspects of S, M and L cones.

A

S cones: 5-10% , absent in fovea

•Ratio of M to L cones differs largely from individual to individual (no impact on color perception)

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16
Q

How does the cone system represent colour?

A
  • 3 kinds of cone opsins sensitive to different light wavelengths – short (S cones) medium (M cones) and long wavelengths (L cones)
  • Not exactly the same as blue, green and red colours but very close to these colour ranges
  • Combined activation of different cones and higher level processing in the brain allow us to see multiple colours
17
Q

How can we detect luminance contrasts?

A

on-center and off-center ganglion cells detect luminance contrasts

18
Q

What is receptive field?

A

part of visual field that one cell monitors – can be seen as having a center and surround.

19
Q

What cells constitute retinal circuitry?

A
rods and cones
bipolar cells
ganglion cell
amacrine cells
horizontal cells
20
Q

What happens to the cells that constitute retinal circuitry when the light falls on the center of their receptive field?

A
Center cone hyperpolarizes, 
bipolar on-center cell depolarizes, 
bipolar off-center cell hyperpolarizes, 
on-center ganglion cell fires action potentials, 
off-center ganglion cells shut down
21
Q

What happens to the cells that constitute retinal circuitry when the light falls on the receptive field’s surround?

A
Center cone depolarizes, 
bipolar on-center cell hyperpolarizes, 
bipolar off-center cell depolarizes, 
on-center ganglion cell shuts down, 
off-center ganglion cells fires action potentials
22
Q

What is the role of glutamate on mGluR6

A

-> - depolarisation

23
Q

What is the role of glutamate on AMPA kainate?

A

-> + hyperpolarisation

24
Q

What is the main usefulness of center-surround receptive fields?

A

emphasize edges

25
Q

What are the function of horizontal cells?

A

Center-surround antagonism in light adaptation

26
Q

Light on center: Horizontal cells

A

horizontal cells release an inhibitory transmitter that maintains cones in a slightly hyperpolarized state (light transduction)

27
Q

Light off center

A

hyperpolarization of the horizontal cell reduces the amount of inhibitory transmitter and these cones become depolarized (opposite of light transduction)

28
Q

Which cells are responsible for light adaptation?

A

Horizontal cells

29
Q

How do … cells achieve light adaptation?

A

Off-center cones influence the signal in on-center cones through inhibition by horizontal cells.
Light off-center deactivates inhibition in horizontal cells (through hyperpolarization in off-center cones). This reduces the amount of inhibitory transmitter and these cones become depolarized (opposite of light transduction)

30
Q

Summary

A

Rods and cones contain photoreceptors activated by light
•Dark current: cation channels gated by cGMP are open, cells are depolarized
•Light: reduction in cGMP through G-coupled photoreceptors, closing of cation channels, cells are hyperpolarised
•Rods: sensitive to light, low spatial resolution, slow recovery of current, many rods connect to one bipolar cell
•Cones: very high special resolution and not sensitive to light (visual acuity), color, sharp response, one-to-one connection to bipolar cells.
•On and off-center cells for contrast detection
•Light adaptation: the intensity of spot illumination depends on the background illumination. Much of the surround antagonism arises via lateral connections by horizontal cells