Vision and optical illusions Flashcards
(41 cards)
What is bottom-up vs top-down in vision?
Bottom-up: raw sensory input from eyes to brain. Top-down: brain influences perception through prior knowledge, expectations, and focus. Vision relies heavily on top-down processing.
What is the concept of “inverse optics” in vision?
It refers to the brain interpreting light reflected off objects, not the source. This reflection helps us perceive texture, shape, and lightness.
What range of the electromagnetic spectrum can humans see?
~380–750 nm. Light outside this range (e.g., infrared, ultraviolet) is invisible to humans.
// 1nm
What does the amount of light dictate vs the pattern of light
amount of light = brightness
pattern = shape and texture
photon
particle of light - represents one wavelength of electromagnetic radiation
fast vs slow vibration impact on wavelength
fast: shorter wavelength = greater energy
slow: longer wavelength, less energy
4 ways light interacts with matter
absorption
- absorbed by the matter and converted to energy
reflection
- light bouncing off an obstacle
diffraction
- light bending around an obstacle
refraction
- change in direction of light when passing from one medium to another
what 4 structures help focus the light onto the retina
lens (curved, bends light), corona (transparent covering over the eye), pupil (controls amount of light to enter), iris (coloured part of the eye)
What things influence pupil dilation and constriction
Light levels, Automatic nervous system, drugs and age
constrict = bright light
dilate = low light
lens accomodation
modify focal length of the eye by changing the curvature of the lens
- adjust to seeing near and far objects
- focusing
cataracts
lens losing transparency due thickening of the lens
- happen with age, UV exposure
hyperopia
far sightedness
- far objects seem clearer than near sighted objects
retina
lines the back of the eye
- contains photoreceptors (rods and cones)
order of light to brain
light, retina, photoreceptors, bipolar cells, retinal ganglion cells, out axons from optic nerve, some cross at optic chiasm and go to LGN of thalamus, remaining little bit follow optic nerve to optic tract to LGN. from here goes from v1,v 2,v3,v4,v5.
% of visual info going to LGN and Superior Colliculus
80% LGN, 20% Superior colliculus
Rods
- located in periphery
- peak absorption -500nm
- good for low light conditions (scotopic)
- low acuity
cones
- located very central near the fovea
- absorption 440 (blue), 530 (green), 560nm (red)
- used in higher light bright conditions (phototopic vision)
- high acuity
photopic vs scotopic
photopic: bright light relying on cones for colour perception
scotopic = low light relying on rods and black and white vision
dark adaptation curve
the dark adaptation curve shows how the eyes sensitivity to light increases over time when transitioning from a bright to dark environment
two phases:
- cones dominate first portion of graph showing the decline of cone intensity to about 10mins, can only see some detail in dim light but not a lot
- rod adaptation take over the rod cone break, becomes very sensitive overtime allowing for vision in dim conditions this vision is low acuity (not sharp and no colour)
number of rods vs cones
more rods (multiple synapse onto one bipolar cell)
- amplify the signal sent to BP cells
- 95 million rods
- low acuity peripheral vision
less cones:
one cone per ganglion cells
- 4.5million cones
- high acuity central vision
fovea
tiny depression in centre of the macula (part of the retina
- responsible for high acuity detailed vision where light is focused when looking at something
- cones located around fovea
Rods inhibitory
rods are inhibited by light
- stop releasing glutamate when
no light = rod is depolarised (excited), activated bipolar cell which activates ganglion cell
cones excitatory and inhibitory
glutamte will open or close differing ion channels
when light hits cone it can either inhibit or active Off or On bipolar cells
On bipolar cells are HYPERpolarised by glutamate
Off bipolar cells are depolarised by glutamate
On/off off/on centre surrounds
receptive field organisation of retinal ganglion cells and bipolar cells
improtant for how we detect contrast, edges and changes in light