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Motion detection
Delay and compare
Measure images at one place and time and then later at another place and time
Velocity = Distance/Time
In a motion detector, the left signal is delayed so that both signals arrive at the comparator at the same time so that it can detect motion
Our perception depends on the output of these motion detectors (therefore making the design and implementation of these detectors important)
Apparent motion
The perception of movement between frame 1 and frame 2
We might seem smooth movement when they are just two snapshots in time
“Static” motion illusion
We might see motion when it might not exist → movies (frames), illusions
This static illusion works by micro-saccades (short movements of the eye), as stationary vision likely causes an image to fade
The correspondence problem
When apparent motion between two frames is more difficult when there are multiple objects - we don’t know exactly which object went where
Nearest neighbour matching
Solution to the correspondence problem
Matches the objects to the nearest one possible, even if this is not actually the case
Common fate
A gestalt grouping rule
The tendency to group things together if they are moving in the same direction e.g. a flock of birds
Aperture problem
A gap in an area is so small that it affects the perception of the object’s movement of direction
E.g. barberpole illusion
Barberpole illusion
Pole goes horizontally with the stripes originally being diagonal
However, because of the small aperture (visual space), it makes the direction and edge ambiguous and makes it look like the pole/stripes are going upwards
Also happens if you change the shape of the aperture (egdes)
Optic flow
The pattern of retinal motions that we see if we move towards or away from an object
Gives useful information about speed and direction of “heading”
e.g. first example = Focus of expansion
Corollary discharge
When the brain sends signals to the eye muscles to move the eyes around, it also sends a copy (efference copy) to the visual processing area
This tells the brain that we are about to move our eyes
If the 2 signals match, this suggests we have moved our eyes ourselves
However if they don’t match, it suggests the external environment has impacted our perception
Area V5/MT
Area containing neurons that detect motion + direction
A study involving a monkey and dots going different directions detected particular V5 activity in response to certain directions more than others
This area is made up of component motion detectors with smaller receptive fields
MSTd → detects self motion, optic flow (rotation etc)
MSTv → detects other objects and trajectories
FST (Fundal Superior Temporal area) → Detecting action in 3D objects rather than 2D
Area V5/MT in humans
Humans have hMT+ in our visual area
Areas V3 (dynamic form) and posterior Superior Temporal Sulcus (pSTS) are important for interactions between form and motion pathways
Recent experiments on inputs from vestibular system (self-motion, balance etc) to motion sensitive cortical areas
The study of biological motion
Experiments connect lights to parts of the body - observers can detect ‘human motion’
These lights can express identity, emotion and gender
Different movements and arrangements can convery how a person ‘knocks’ on a door
When the dots are scrambled, it is a lot harder to see the motion
Area sensitive to biological motion
Posterior Superior Temporal Sulcus
Biological motion in Autism
Even though both non-autistic and autistic participants could detect motion equally well, non-autistic group had access to different brain pathways compared to autistic
The autistic group tended to see it as a series of snapshots compared to motion directly in non-autistic participants
Due to larger receptive fields in ganglion cells, complex cells and V5, leading to less fine detail of movement