Title: WHY DOES THE BRAIN HAVE SO MANY VISUAL AREAS
1WHY DOES THE BRAIN HAVE SO MANY VISUAL AREAS?
- Neuroscience 500
- March 2005
Jody Culham Department of Psychology, University
of Western Ontario London, Ontario,
Canada culham_at_uwo.ca
2Reading
- Kaas, J. H. (1989). Why does the brain have so
many visual areas? Journal of Cognitive
Neuroscience, 1, 121-135. - Allman, J. (2000). Primate brains (Ch. 6, pp.
122-157). Evolving Brains. New York Scientific
American Library. - Gazzaniga, M., Ivry, R. B. Mangun, G. R. (with
L. Krubitzer) Evolutionary perspectives (Ch. 14,
pp. 577-596 only). Cognitive Neuroscience The
Biology of the Mind (2nd ed.). New York Norton. - pdfs of papers and full color lecture slides are
available on my web site - http//defiant.ssc.uwo.ca/Jody_web/courses.htm
3Topics
- How is the visual system organized into areas?
- What defines a visual area?
- How can we determine visual areas in the human?
- How do brains evolve?
- So why are there so many visual areas and how did
they get that way? - What questions remain?
4Who knows, who cares, why bother?
- Vision is arguably one of the best understood
neuroscience systems. Understanding vision often
elucidates general principles of neural function. - Cognitive neuroscience needs to use as much data
from as many paradigms as possible to understand
something as complicated as the brain. This
poses concerns in comparing between species.
Understanding homologies vs. new areas is
valuable. - Thinking about evolution and how the brain got
that way is highly valuable to the
neuroscientist. - Neuroimaging studies often publish long lists of
activated regions that are hard to compare
between studies. My opinion is that imaging has
been most successful where specific areas have
been clearly identified and thoroughly studied.
5Part 1 How is the visual system organized into
areas?
6Primary Visual Pathway
- Retina
- Thalamus
- Lateral Geniculate Nucleus (LGN)
- divided into magno and parvo layers
- Primary visual cortex (V1)
- Extrastriate visual areas
- Each visual hemifield projects to the opposite
hemisphere
7Beyond V1
- primary visual cortex (V1)
- extrastriate cortex
- Over 30 visual areas
- Complex organization
- Visual areas make up 40 of monkey brain
Macaque Brain
Flattened Cortex
Source Van Essen et al., 2001
8Why are there so many visual areas?
Source Felleman Van Essen, 1991
Source Mapping the MInd cover image
9Two visual pathways
- The two visual processing streams for different
visual percepts - What (ventral stream)- object recognition
- main input from slow and detailed parvo system
- Where or How (dorsal stream) - spatial
perception, motor planning - main input from quick and dirty magno system
Source Mishkin Ungerleider, 1982
10Wiring the Streams
Dorsal
Ventral
11The What Pathway
- Other Visual Areas
- contain more complex receptive fields
- Temporal Lobe
- contains many specialized areas for recognizing
various things
body motion
faces
places
bodies
objects
12Complex Receptive Fields
Face neurons in the monkey brain
13The Where or How Pathway
grasping and reaching
attention
head movements
- Parietal Lobe
- contains many specialized areas for using vision
to guide actions in space
motion perception
eye movements
14Part 2 What Defines a Visual Area?
15What is a Visual Area?
- Function
- an area has a unique pattern of responses to
different stimuli - Architecture
- different brain areas show differences between
cortical properties (e.g., thickness of different
layers, sensitivity to various dyes) - Connectivity
- Different areas have different patterns of
connections with other areas - Topography
- many sensory areas show topography (retinotopy,
somatotopy, tonotopy) - boundaries between topographic maps can indicate
boundaries between areas (e.g., separate maps of
visual space in visual areas V1 and V2
16Each visual area has a map
calcarine sulcus
horizontal meridian (HM)
VM
VM
HM
HM
VM
VM
left occipital lobe
left occipital lobe
right occipital lobe
right occipital lobe
vertical meridian (VM)
- Each visual area contains a map of visual space
- polar coordinates
- eccentricity runs posterior-anterior
- phase runs superior-inferior
- The map for visual area V1 lies along the
calcarine sulcus
Source Jody Culham
17Map boundaries divide visual areas
Consider just one hemifield/hemisphere
calcarine sulcus
V1 upper
horizontal meridian (HM)
V1 lower
VM
HM
VM
left occipital lobe
left occipital lobe
left occipital lobe
vertical meridian (VM)
- Adjacent maps are divided by specific boundaries
(in vision, the horizontal and vertical meridia) - Adjacent maps are mirror imaged
Source Jody Culham
18MT A Case Study
- Middle temporal area of the macaque monkey
- Meets most criteria for an area
- Has an apparent human equivalent
19MT Function
- Single unit recording
- Single neurons in MT are tuned to the direction
of motion - Neurons are arranged in direction hypercolumns
within MT cortex
20MT Function
- Lesions
- lesions to MT lead to deficits in perceiving
motion - Microstimulation
- stimulation of a neuron affects the perception of
motion - e.g., if you find a neuron with a preference for
upward motion, and then use the electrode to
stimulate it, the monkey becomes more likely to
report upward motion
21MT Architecture
- MT is stained with cytochrome oxidase (which
indicates high metabolic activity)
22MT Connectivity
- MT receives direct input from V1
- largely from the fast magno pathway cells
- MT projects to specific higher-level areas
- MT is an intermediate level visual area
23MT Topography
- MT has a topographic representation of visual
space
24Part 3 How can we determine visual areas in the
human?
25Tools for mapping human areas
- Neuropsychological Lesions
- Temporary Disruption
- transcranial magnetic stimulation (TMS)
- Electrical and magnetic signals
- electroencephalography (EEG)
- magnetoencephalography (MEG)
- Brain Imaging
- positron emission tomography (PET)
- functional magnetic resonance imaging (fMRI)
26How well are human visual areas mapped?
27An analogous mapping situation?
28How can we map human (visual) areas?
- Look for homologues (or analogues) of known
primate areas - Example Human MT
- Look for areas that may participate in uniquely
human abilities - Example Language, calculation, social
interaction areas
29Back to our case study MT
MT
intermediate
V1
A patient with bilateral lesions to MT can no
longer perceive motion (Zihl et al., 1983)
A temporary disruption to human MT interferes
with motion perception (Beckers Zeki, 1995)
30fMRI of Human MT
Video MT_on_rotatingbrain.mpg
Video V1MTmovie.mpg
fMRI in humans reveals MT
Moving vs. stationary dots activates V1 and
MT Flickering vs. stationary checkerboards
activates V1
31Is Human MT an Area?
- Function
- properties of human MT are highly similar to
macaque MT - Architecture
- stains for cytochrome oxidase (like monkey MT)
- Connectivity
- not investigated
- Topography
- recent fMRI evidence finds a retinotopic map
within human MT - Evolutionary Relationships
- the existence of primate MT makes it likely that
humans have a homologue - the position of MT is considerably lower in
humans than monkeys
predicted location
32Part 4 How do Brains Evolve?
33A Reminder About Evolution
- Evolution is a tree not a line
34Evolution of Areas
- With evolution
- brains become larger (volume-wise)
- brains become more convoluted (more surface area)
- proportionately less cortex is devoted to primary
somatosensory and motor areas - there is more room for association cortex
35Evolutionary Relationships
- Homology
- a structure, behavior or gene that has been
retained from a common ancestor - e.g., monkey hand and human hand
- Homoplasy (or Analogy)
- structures that look the same but do not
necessarily have the same common ancestor - e.g., bat wing and fly wing
36Evolutionary Comparisons
- Knowledge of areas and topography can be useful
in anticipating human areas - Early visual areas show a good deal of similarity
between human and monkey (based on retinotopic
boundaries)
Macaque
Human
(fMRI)
(single neurons)
Tootell et al., 1996
37MT Evolution
- MT exists in a variety of primate species
- In each of the three primate species, MT has the
same types of cytoarchitecture and connections - An MT-like area exists in tree shrews but its
not yet clear whether it is homologous to primate
MT
38Primate vs. Cat Motion Areas
- A motion area (PMLS, posteromedial lateral
suprasylvian area) exists in the cat - Cat PMLS is unlikely to be a homologue of primate
MT - similar motion-responsive properties
- but does not exist in intervening species
- example of homoplasy
- illustrates independent evolution of similar areas
39Part 5 So why are there so many visual areas and
how did they get there?
40More brain, more visual areas
41Why not one really big visual area?
V1
42Why not a really big visual area?
- As areas become larger, longer interconnections
are required - Limits on cortical thickness and connections may
constrain max area size
43Parallel processing is more efficient
- Teach neural network to identify what and
where - One neural network with 18 nodes (neurons)
devoted to both tasks - versus
- One neural networks with two streams of 9 nodes
each (total 18) - After 300 training trials, the two stream model
outperformed the single-system model
Rueckl, Cave Kosslyn, 1989
44Different Tasks Require Different Information
- different regions may need to use different
coding systems
dorsal stream viewer-centred
ventral stream object-centred
45Wiring Constraints
David Van Essen proposes that as the brain
develops, areas that are richly interconnected
will be pulled together to form a gyrus (and
those that are weakly interconnected form sulci).
46Sulcal Formation V1-V2
The V1/V2 border provides one example of two
richly interconnected areas that form a
gyrus. This arrangement also explains why maps
in V1 and V2 are mirror images of each other!
calcarine sulcus
Source Van Essen, 1997
47Optimized Connections
- Multidimensional Scaling
- strength of connections can be used to infer
spatial layout - expected layout of visual areas matches anatomy
amazingly well
Parietal
Occipital
Temporal
Malcolm Young
48Its a small world after all
- Small world theory is being applied to
- social networks
- sexual networks
- terrorist networks
- Six degrees of Kevin Bacon
- Internet hyperlinks
- transportation networks
- THE BRAIN!
49Big brain Small world
50Optimized Connections
- Multidimensional Scaling
- strength of connections can be used to infer
spatial layout - expected layout of visual areas matches anatomy
amazingly well
Parietal
Occipital
Temporal
Malcolm Young
51General Organization Patterns
Malach et al., 2002, TICS
52(No Transcript)
53General Organization Patterns
Hasson et al., 2003, Neuron
54Gene mutations
Pinky the Brain experiment
Chenn Walsh, 2002, Science
- simple gene mutations can have drastic
consequences (e.g., changing one protein can
change encephalization of a mouse)
55Gene mutations
- Gene mutations can lead to a duplication of areas
- These areas can be mirror symmetric with existing
areas - Note This is one of many theories
56Part 6 What questions remain?
57Are humans just morphed monkeys?
Figure B shows the macaque monkey visual areas
from A morphed onto human cortex based on the
placement of sulcal landmarks (Van Essen et al.,
2001). fMRI activation suggests the areas have
moved somewhat. Can we assume humans are just
morphed monkeys? In some areas the human
cortical surface area is slightly larger than in
the macaque (e.g., visual cortex 2X) in others
it is considerably larger (e.g., parietal cortex
20X) Are individual areas larger? Are there
more areas?
58Or are there expansion sources?
Frontal Eye Fields
MT
predicted location
predicted location
- most human functions seem to be located in
- inferior parietal cortex
- superior temporal cortex
- prefrontal cortex
Calculation
Language
59Did new functions hijack old areas?
- ventral premotor cortex in monkeys
- mirror neurons
- ventral premotor cortex in humans
- mirror neurons
- Brocas area language
- Rizzolatti suggests speech evolved out of hand
gestures and imitation
Rizzolattis Mirror Neurons
60How much plasticity is there?
Experience seems to play a huge role
Are species differences due to genes or inputs?
61How does Humpty Dumpty get put back together
again?
- The Binding Problem
- If an image (e.g., Humpty Dumpty) has each of its
attributes (form, color, motion) processed in a
different cortical area, how come we perceive the
unified image?
- One possible solution
- Feedback loops may lead to synchronous firing
between neuronal populations in different areas
that encode the same attribute (e.g., spatial
location)