1. Cognitive Architectures
Perception - Vision
Based on book Cognition, Brain and Consciousness ed. Bernard J. Baars
courses taught by Prof. Randall O'Reilly, University of Colorado, and
Prof. Włodzisław Duch, Uniwersytet Mikołaja Kopernika
and
Janusz A. Starzyk

2. Motivation
Perception is comparatively the easiest to understand although for many specific questions there are no clear answers.
General questions:
Why does the primary visual cortex react to oriented edges?
Why does the visual system separate information into the dorsal stream, connected to motion and representation of object locations, and the ventral stream, connected to object recognition?
Why does damage to the parietal cortex lead to spatial orientation and attention disorders?
In what way do we recognize objects in different places, orientations, distances, with different projections of the image onto the retina?

3. Introduction
The purpose of vision: ‘to know what is where’ (David Marr)
The visual perception is far more complicated than simply taking a picture with digital camera
The camera doesn’t really do anything with this image and doesn’t have any knowledge about what is stored in the image

4. Introduction Knowing what: perceiving features, groups and objects
Studies of human visual perception and neuroscience suggest that there are many levels of perception.
The human brain appears to process basic visual features, such as color, orientation, motion, texture and stereoscopic depth.
Neurons are highly tuned to specific features like a line at particular angle, a particular color, or particular motion detection.
The activity of each neuron represents only a small part of the visual field. How is the brain able to combine this information across many neurons?
The brain is able to organize basic feature elements into organized perceptual groups.
Psychologists proposed the Gestalt laws of perceptual grouping, such as the laws of similarity, proximity, good continuation, common fate and so forth

5. Perceptual grouping Grouping by similarity: Grouping by proximity:
White dots grouped with white dots, squares with squares
Grouping by proximity:
Here we perceive two separate groups of dots that are near each other
Grouping by good continuation:
On the left we perceive a single object.
When the same lines are separated we do not

6. Functional organization of the visual system
Visual pathway

7. Visual pathways
Visual pathways: retina => lateral geniculate nucleus (LGN) of the thalamus => visual radiation => area of the primary cortex V1 => higher levels of the visual system => associative and multimodal areas.
V1 cells are organized in ocular dominance columns and orientation columns, retinoscopic. Simple layer 4 cells react to bands with a specific slant, contrasting edges, stimulus from one eye. A substantial part of the central V1 area reacts to signals from fovea, where the density of receptors is the greatest.

8. Functional organization of the visual system
The hierarchical organization begins in the retina, passes through the lateral geniculate nucleus (LGN - part of the thalamus), reaching the primary visual cortex V1, from where it's distributed further.
(c) Tralvex Yeap. All Rights Reserved 8

9. Functional organization of the visual system
Objects in environment are projected to the back of the eye – the retina.
Retina contains millions of photoreceptors

10. The retina Two types of light-sensitive photoreceptors Cones
cone-shaped
less sensitive
operate in high light
color vision
Rods
rod-shaped
highly sensitive
operate at night
gray-scale vision

11. The retina
The signals from photoreceptors are processed by a collection of intermediary neurons, bipolar cells, horizontal cells and amacrine cells, before they reach the ganglion cells

12. Retina The retina is not a passive camera registering images.
Crucial rule: enhancing contrasts underlining changes in space and time, strengthening edges, uniformly lit areas are less important.
Photoreceptors in rods and cones,
3-layer network, ganglion cells =>LGN.
Receptive fields: areas, which stimulate a given cell.
The combination of signals in the retina gives center-surround receptive fields (on-center) and vice versa, detects edges.
Each individual field of cells can be modeled as a Gaussian model, so these fields are obtained as a difference of Gaussians (DOG).

13. On-center off surround ganglion cells
No stimuli:
both fire at base rate
Stimuli in center:
ON-center-OFF-surround fires rapidly
OFF-center-ON-surround doesn’t fire
Stimuli in both regions:
both fire slowly
Stimuli in surround:
OFF-center-ON-surround fires rapidly
ON-center-OFF-surround doesn’t fire

14. On-center off surround ganglion cells
on-center cell
David Hubel & Torsten Wiesel
Received Nobel price for their
discovery of on-center off-surround
cells in retina

15. On-center off surround ganglion cells
Retina ganglion cells receive both excitatory and inhibitory inputs from bipolar neurons
In the figure shown, the ganglion cell receives excitatory inputs from cells corresponding to the on-center region, and inhibitory inputs from the off-center region

16. On-center off surround ganglion cells
Original image
Image based on edges
Lateral inhibition is important in enhancing neural representation of edges, where the light intensity changes sharply and indicate a presence of contours, shapes, or objects.
Uniform parts of a picture are less interesting.

17. On-center off surround ganglion cells
Sometimes this later inhibition leads to a surprising visual illusions as shown on this figure.
Notice black dots appear on intersection of white lines.

18. Retinal ganglion cells
There are two types of ganglion cells in the retina:
Large magnocellular ganglion cells, or M cells, carry information about:
Movement
Location
depth perception.
Smaller parvocellular ganglion cells, or P cells, transmit signals that pertain to:
Colour
Form
texture of objects in the visual field.

19. Lateral geniculate nucleus (LGN)
From the eye, retinal ganglion cells send their axons to a structure in the thalamus called lateral geniculate nucleus (LGN)
The inputs from the nasal portion of each retina must cross at the optic chiasm to project to the opposite LGN

20. LGN pathway The M cells send their information to layers 1 & 2 of LGN.
The P cells send their information to layers 3-6.
So, layers 3-6 are involved in processing information concerning fine detail and color.
Layers 1 & 2 process information concerning movement.

21. Pathways in visual system
Propagation of the visual input from the left and right visual fields.
Signals propagate through eye, retina, optic nerve, chiasm, optic tract, LGN to visual cortex V1

22. Lateral geniculate nucleus
Signal compression – partly already done in the retina.
Different types of information find their way to different LGN layers.
Intermediate station – all sensory signals (except olfactory) go through different nuclei of the thalamus.
Dynamic information processing: steering attention and fast large-celled pathway reacting to motion.
Retroactive projections V1=>LGN are an order of magnitude more numerous than LGN=>V1 (role - prediction).
The competitive dynamic selects signals from the visual field, especially involving motion.

23. LGN of the Thalamus
Parvocellular layers 3-6
Magnocellular layers 1& 2

24. Primary visual cortex V1
Neurons in V1 are sensitive to a whole host of visual features, not seen in the LGN, like orientation, direction of motion, color differences, or binocular disparities.
Orientation helps to detect edges and contours.
Direction of motion is important to determine dangerous moves of an attacker.
Color helps to differentiate and identify objects particularly in a camouflage environment.
Binocular disparities between images in two eyes allow us to perceive stereo-depth when we look at object with both eyes.

25. Primary visual cortex V1
Neurons in V1 respond with different strength to orientation edges, depending on location of their receptive fields.
Neuron’s response is strongest if the excitation aligns with its receptive field.

26. Edge detectors
Contrasting signals points from the LGN are organized by the V1
cortex into edge detectors oriented at a specific angle.
Simple V1 cells combine into edge detectors, enabling the determination of shapes, other cells react to color and texture.
Properties of edge detectors: different orientation; high frequency = fast changes, narrow bands;
low frequency = gentle changes, wide bands;
polarization = dark-light or vice-versa, dark-light-dark or vice-versa.

27. Representation in the V1 cortex
Oriented edge detectors can be created by correlational Hebbian learning based on natural scenes.
What happens with information about color, texture, motion?

28. Retinoscopic maps in V1
The spatial position of the ganglion cells within the retina is preserved by the spatial organization of the neurons within the LGN layers. The posterior LGN contains neurons whose receptive field are near the fovea.

29. Area V1: The Primary Visual Cortex
V1 is made up of 6 layers (no relation to 6 layers in LGN).
LGN sends axons to layer IV of V1.
M and P cells are separate.
Right and Left eye are separate.

30. Hierarchy of visual processing
From retina, LGN, V1, through V4 and to ventral temporal cortex (VTC) neurons gradually respond to more complex stimuli:
Retina and LGN extract small dots
In V1 small dots are combined into edges,
In V4 edges are combined into simple shapes and color features
In VTC simple shapes are combined into objects

31. Extrastriate visual areas – outside of V1
Flattened map of higher visual areas
V1 sends signals to many higher visual areas, including areas such as V2, V3, V4 and motion-sensitive area MT.
Area V4 is important for the perception of color and some neurons in V4 respond to more complex features or their combination (like corners or curves).
The middle-temporal area (MT), is important for motion perception.
Almost all of the neurons in MT are direction-selective, and respond selectively to a certain range of motion directions or patterns of motion.

32. The ventral and dorsal pathways: knowing what and where
The projections from V2 to higher areas in the cortex can be roughly divided according to two major parallel pathways: a ventral pathway to temporal lobe (what) and a dorsal pathway to parietal lobe (where)
The ‘what’ pathway includes ventral areas like V4, LOC, and IT

33. Two streams where?/what?
depth
direction
“where” pathway
“what” pathway
orientation
shape
color
Recognized
Object ready
for perception
“Where" = large-celled pathway, heading for the parietal lobe.
"What"= small-celled pathway heading for the temporal lobe (IT).

34. The ventral and dorsal pathways: knowing what and where
In the dorsal pathway, signals from V1 travel to dorsal areas like MT and V3A, which then send major projections to many regions of the parietal lobe.
In the ventral pathway, many signals from V1 travel to ventral areas V2, V3 and V4 and onward to many areas of the temporal lobe.
Dorsal and ventral pathways in a monkey brain

35. Two streams where?/what?
- temporal lobe
Where?
- parietal lobe
Milner and Goodale (1995): visual pathways don't so much determine where and what, as much as they enable action and perception.
There is also the old limbic pathway, enabling rapid action in dangerous situations (after which follows a wave of fear).

36. Two streams
Ungerleider and Mishkin (1982): there exist two notably divided pathways for processing visual information, running from the eye.
Large-grained PA retina cells, 3 types of photoreceptive cones, large receptive fields, rapidly-conducting axons, activation for light in a wide band.
Small-grained PB cells, 1 or 2 types of photoreceptive cones, small receptive fields, slowly conducting axons, recognize color oppositions.
Large-celled pathway: runs to two large-celled LGN layers, it's characterized by a low spatial resolution, high sensitivity to contrast, rapid signal transfer, without information about color. The small-celled pathway has 4 small-grained layers in the LGN, high spatial resolution, color, slower information transfer, low sensitivity to contrast.

37. Areas involved in object recognition
Lateral occipital complex (LOC)
The lateral occipital complex seems to have a general role in object recognition and responds strongly to a variety of shapes and objects.
Presumably neurons in this region respond best to different kinds of objects.
Fusiform face area (FFA)
Human neuroimaging studies have shown that there is a region in the fusiform gyrus, called the fusiform face area (FFA) that responds more strongly to faces than to just about any other category of objects.
This region responds more to human, animal and cartoon faces than to a variety of non-face stimuli.
Neurons in this area specialize in facial expression, particular identity or viewpoint (e.g. profile)
Parahippocampal place area (PPA)
The parahippocampal place area is another strongly category-selective region that responds best to houses, landmarks, indoor and outdoor scenes.
This area responds weakly to faces, body parts, and animals.

38. Hierarchical and interactive theories of vision
Is it possible to invoke visual experience without seeing?
Yes we can bypass retina and LGN and stimulate area V1.
However, it seems impossible to recover full visual experience from higher visual areas bypassing primary visual cortex.
Hierarchical and interactive theories of vision
According to hierarchical theory, visual consciousness is organized in a hierarchical fashion with increasingly higher visual areas being more closely related to our internal conscious experience. But if this is the case how to explain awareness of all details in the observed image?
The interactive theory of visual consciousness emphasizes interactions between lower and higher visual areas where higher areas send feedback signals down to early visual area.

39. Some answers
Why does the primary visual cortex react to oriented edges? Because correlational learning in a natural environment leads to this type of detector.
Why does the visual system separate information into the dorsal pathway and the ventral pathway?
Because signal transformations extract qualitatively different information, strengthening some contrasts and weakening others.
Why does damage to the parietal cortex lead to disorders of spatial orientation and attention (neglect)?
Because attention is an emergent property of systems with competition.
How do we recognize objects in different locations, orientations, distances, with different images projected on the retina?
Thanks to transformations, which create distributed representations based on increasingly complex and spatially invariant features.