diagram
kno we know there are different types of photoreceptor - rods and cones - there are 3 types of cones that form the basis of colour vision
that info is then compresssed by the retina into an effiecient code, sent back via the optic nerve to the LGN where we have layers and parallel processing streams doing different things
parvocellular layers - carry info on fiene detail and differences between the red and green cones
kornivocellular layers - signall differences betwene short wavelength of blue cone and mixure of red and green which is the yellow cone
also have magnocellular layers that are important in signally temporal information changes - motion perception is based on info in this stream - then sends info to layers in area V1 specifically MT or V5 where is the motional centre of your brain
a real sense?
spooky movements
movements that are there within an image that is clearly stationary
due to high contrast and low contrast colours in the edges to give impression of edge movement of the image
this illusion works on cats - so have similar things in the visual system that we have
frogs are blind to anything that isnt moving
motion aftereffect (waterfall illusion)
apparent motion
everytim you watch tv you get the illusion of motion nothing is actually moving its a series of still frames
tv has about 60 frames a second and movies about 24 a second
they present them fast enough that your brain interprets the still images as one moving image
if the frames are too slow with too much time between them we dont see good/smooth movement
apparant motion
hard to detect with one dot moving easier to see when following more than one dot
movement detector
explains apparent motion as all we need is something to be at point a and then a little time later point b the stuff inbetween doesnt count - as long as the timing and distance is right
random dot patterns and random dot kinematograms
Braddick (1974, 1980)
direction selective cells
visual areas
there are over 32 visual areas
some of them we know a lot about eg area V1/the striate cortex, MT - middle temporal area/V5 first discovered in new world primates
- those cells that are directionally selective in V1 send their output to V5 - its where we concentrate the information about motion - nearly all cells in area MT/V5 are direction specific
direction selective cell area - MT (snowden et al, 1992)
Neurons in area MT show strong directional selectivity.
Here the neuron responds strongly to motion down to the left.
In MT we have direction of motion columns
Mikami, Newsome and Wurtz (1986) - Newsome, Mikami and Wurtz (1986)
combining area MT neurons with apparent motion
Mikami, Newsome and Wurtz (1986) - Newsome, Mikami and Wurtz (1986) - results
plot out for lots and lots of cells
look at the biggest interval and jump they can stand gets graph below
dark dots mean the cell was directionally selected and could tell the difference between preferred and null and the other means not reliable
these neurons could make a jump of about 2 degrees and no more than 100ms - these cells are in the periphery so can see much bigger jumps than centre of vision - same for our MT cells aswell
also if you stimulate these cells to make them fire you can make animals see motion
Human MT - imaging studies
put someone in a brain scanner and get them to look a pictire of boring random patterns and compare the activity you get in the brain when the patterns are staionary compared to when the patterns are moving
- when you do that you get two areas of activity - one at the very back = Area V1and area V5/MT - similar to NWP
enigma pattern
people can see motion in this illusion even though its completely stationary but there are some individual differences
some people cant see anything
can show this pattern and look at what happens in area MT
Zeki, Watson and Frackowiak (1993)
Motion blindness (Cerebral Akinetopsia)
speed
Snowden et al (1998)
key concepts
reading - two ways of seeing movement
⭐ Two motion systems:
Retinal movement system:
Detects motion across the retina
Works when eyes are still, object moves
Eye–head movement system:
Uses signals about our own eye movements
Allows motion perception when retinal image is stable (e.g., tracking, after-images)
⭐ Stability problem:
Eye movements cause images to move on retina
Yet the world appears stable
Brain must subtract self-caused motion
⭐ Two theories:
Charles Scott Sherrington (Inflow):
Uses eye muscle feedback
Hermann von Helmholtz (Outflow – correct):
Uses efference copy (copy of motor command)
⭐ Key experiments:
Tracking moving object → both correct
After-image moves with eye → both correct
Poking eye: world moves → supports Helmholtz
Eye poke + after-image: no movement → Helmholtz
Command to move eyes (but prevented): world moves → Helmholtz
⭐ Key takeaway:
Motion perception = retinal signals + efference copy
Hermann von Helmholtz’s theory explains:
Stable world despite eye movements
After-image effects
Illusions when eyes are manipulated
a motion detector
⭐ Why motion detection is needed:
Must determine direction + speed
Need timing info (which receptor fires first), not just activation
⭐ The basic problem:
A → B and B → A both activate the same receptors
Without timing → no direction information
⭐ Delay-and-compare detector:
Two receptors (A & B) sample positions
Signal from A is delayed
Detector fires only if signals arrive simultaneously
Outcome:
A → B → fires ✅
B → A → no firing ❌
→ Produces direction selectivity
⭐ Limitation:
Works only at a specific speed (timing must match delay)
⭐ Real-world analogy:
Speed cameras: distance ÷ time between two images = speed
Mirrors delay + comparison logic
⭐ Building complex detectors:
Combine leftward + rightward detectors
One excites, one inhibits
Cancels non-directional signals (e.g., flicker)
⭐ Biological evidence:
Direction-selective cells:
❌ Not in retina (primates) or LGN
✅ First in V1
✅ Abundant in V5/MT (motion area)
Other species (e.g., insects) show retinal direction selectivity
⭐ Key takeaway:
Motion detection relies on timing differences between signals
Delay-and-compare explains direction selectivity
Crucial for survival (detecting predators/prey)