The Neurobiology of Space
James Lawley
These
notes are in three parts:
(a) All indented paragraphs are quotes from
In Search of
Memory: The Emergence of a New Science of Mind by Eric R.
Kandel published by Norton in 2007. (
NB. I have emboldened some key concepts.)
(b) The non-indeneted paragraphs contain my reflections on the quotes
(c)
Three exercises Penny Tompkins and I designed to explore the perception of space.
In
his very readable book, Eric Kandel, Nobel prize winner for Medicine or Physiology, intertwines a combination of
cognitive psychology, neuroscience and molecular biology with his own
personal quest to understand memory. The following quotes have been selected
because they relate to the
neurobiology of space
perception. They have been collected together into three sections which
describe the role of:
1. The pyramidal cells of the hippocampus
2. Selective attention
3. A synaptic strengthening mechanism called long-term potentiation.
1. The role of pyramidal cells of the hippocampusIn
1971, John O'Keefe at University College London made an amazing
discovery about how the hippocampus processes sensory
information. He found that neurons in the hippocampus of the
rat register information not about a single sensory modality
— sight, sound, touch, or pain — but about the
space surrounding the animal, a modality that depends on information
from several senses. He went on to show that the hippocampus
of rats contains a representation — a map — of
external space and that the units of that map are the pyramidal cells
of the hippocampus, which processes information about place.
In fact the pattern of action potentials in these neurons is so
distinctly related to a particular area of space that O'Keefe referred to
them as "place cells." Soon after O'Keefe's discovery,
experiments with rodents showed that damage to the hippocampus severely
compromises the animals' ability to learn a task that relies on spatial
information. This finding indicated that the spatial map
plays a central role in spatial cognition, our awareness of the
environment around us. (pp. 281-282)
As
soon as the metaphor of “a map” is used it brings
with it entailments of a ‘map reader’. But,
according to current neuroscience, there is no map reader in the brain,
just synchronised electrical and chemical reactions from which
behaviour emerges. Thus the ‘map’ Kandel refers to is not a map in the
ordinary sense of the word, it’s a configuration of neurons
whose pattern of firing contributes to the animal being able to
navigate round its environment.
[That]
the spatial memory of environments has a prominent internal representation in the hippocampus is
evident even anatomically. Birds in which spatial memory is
particularly important — those that store food at a large number of
sites, for example — have a larger hippocampus than other
birds. London taxi drivers are another case in
point. Functional magnetic resonance imaging [fMRI] revealed
that after two years of [learning ‘The Knowledge’
of the] streets of London, taxi drivers have a larger hippocampus than
other persons of the same age. Indeed, the size of their
hippocampus continues to increase with time on the job.
Moreover, brain-imaging studies show that the hippocampus is activated
during imagined travel, when a taxi driver is asked to recall how to
get to a particular destination. (pp. 305-306)
We
believe that because much the same neurology is involved in imagining doing something and actually doing it, this explains one of the benefits of “making words physical”. David Grove used to
emphasise the need to
facilitate the client to shift from conceptual descriptions which
have no coordinates to
located symbolic representations. Then parts of
the brain that know about space, movement and interactions in the
physical world can be brought into service during the consideration of an
abstract problem or desired outcome.
In
all living creatures, from snails to people, knowledge of space is
central to behavior. As John O'Keefe notes, "Space plays a
role in all our behaviour. We live in it, move through it,
explore it, defend it." Space is not only a critical sense
but a fascinating one because unlike other senses space is not analyzed
by a specialized sensory organ. How, then,
is space represented in the brain? Because we do not have a
sensory organ dedicated to space, the representation of space is a
quintessentially cognitive sensibility: it is the binding problem writ
large. The brain must combine inputs from several different
sensory modalities and then generate a complete internal representation
that does not depend exclusively on any one input.
(pp. 307-308)
Interestingly,
Kandel regards space as a “sense” that is
“generated” by a synthesis of the more traditional
senses.
The
brain commonly represents information about space in many areas and
many different ways, and the properties of each representation vary
according to its purpose. For example, for some representations of space
the brain typically uses egocentric coordinates (centered on
the receiver), encoding, for example, where a light is relative to the
fovea or where an odor or touch comes from with respect to the
body. Egocentric representation is also used by people or
monkeys for orientating to a sudden noise by making an eye movement to
a particular location. For other behaviors, like memory for
space in the mouse or in people, it is necessary to encode the organism's position relative to
the outside world and the relationship of external objects to one
another. For these purposes the brain uses
allocentric coordinates (centered on the world). (p. 308)
Have
you noticed how modern Sat Navs give you a choice to use either ego- or
allo-centric coordinates. The “ego” is the car and
the perspective is either ‘through the windscreen’
or a ‘birds-eye view’. In NLP (Neuro-Linguistic Programming), the use of
egocentric coordinates is called 'associated' or
‘in-time’ and and allocentric coordinates are called 'dissociated' or ‘thru-time’.
From
a Symbolic Modelling perspective it’s not quite so simple.
Egocentric is actually own-body-centric. But because
‘a perceiver’ can move independent of the
ego’s physical body, egocentric and allocentric coordinates
can be used in a variety of combinations. In fact, we doubt
the sole conscious use of allocentric coordinates is possible. Even if
a person is using an map “centred on the world”
they still have to perceive the map
from somewhere.
That’s why it makes a big difference when you turn a map
upside down — the map is still using allocentric coordinates
but your egocentric perspective on those coordinates has changed.
Egocentric
coordinates are common in Clean Language work as a client’s
Metaphor Landscape is usually centred on their body. However,
once a Landscape takes on an independence from its owner, it forms
‘the world’ upon which allocentric coordinates can
be based. Then the Landscape can remain fixed while attention
moves around it using either type of coordinate.
Clean
Space has the effect of turning a client’s egocentric
coordinates into allocentric coordinates by
“nailing their history to the floor so that it can be
examined” as David Grove so grpaphically referred to it.
The
spatial map discovered by O'Keefe differs radically from the egocentric
sensory maps for touch and vision, because it is not dependent on any
given sensory modality. O'Keefe found that as an animal walks
around an enclosure, some place cells fire action potentials only when
that animal moves into a particular location, while others fire when the
animal moves to another place. The brain breaks down its
surroundings into many small, overlapping areas, similar to a mosaic,
each represented by activity in specific cells in the hippocampus. This internal map of space develops within minutes of the rat's entrance into a new environment. (pp. 308-309)
An
analogue in Clean Space is the breaking down of a complex abstract
issue into several small areas, each represented by a verbal or nonverbal description of knowledge. What is new (to us, at
least) is the notion of “overlapping” spaces
— something we want to explore on the day.
Unlike
vision, touch, or smell, which are prewired and based on a
priori [pre-existing] knowledge, the spatial map presents us
with a new type of representation, one based on a combination of a
priori knowledge and learning. The
general capability for forming spatial maps is built into
mind, but the particular map is not. Unlike neurons
in a sensory system, place cells are not switched on by sensory
stimulation. Their collective activity represents the
location where the animal thinks it is. (p. 309)
In some ways "forming a spatial maps" seems parallel language acquisition. A baby comes into the world ready to acquire language but which particular language they learn depends on where and with whom they live.
And
“where the animal thinks it is” is not a single
thought, but multiple perceptions which somehow emerge in consciousness
as an apparently unified representation. Even when you know a visual
illusion is fooling your neurons, it doesn’t stop you
‘seeing’ it as real. The two types of
knowledge are processed in different ways and in different parts of the
nervous system.
2. The role of selective attentionSelective
attention is widely recognized as a powerful factor in perception,
action, and memory — in the unity of conscious
experience. At any given moment, animals are inundated with a
vast number of sensory stimuli, yet they pay attention to only one or a
very small number of them, ignoring or suppressing the rest.
The brain's capacity for processing sensory information is more limited
than its receptors' capacity for measuring the environment.
Attention therefore acts as a filter, selecting some objects for
further processing. This focusing of the sensory apparatus is
an essential feature of all perception. (p. 311)
Attention
also allows us to bind the various components of a spatial image into a
unified whole. [Kandel's mice studies show that] even ambient
attention (the attention that is present in the absence of stimulation)
is sufficient to allow a spatial map to form and become stable for a
few hours, but such a map becomes unstable after three to six
hours. Long-term stability correlates strongly and
systematically with the degree to which an animal is required to pay
specific attention to its environment. Thus, when a mouse is
forced to pay a lot of attention to a new environment, by having to
learn a spatial task at the same time that it is exploring the new
space, the spatial map remains stable for days and the animal readily
remembers a task based on knowledge of that environment. (p. 312)
In
The Principles of Psychology [1890] William James pointed out that
there is more than one form of attention. There are at least
two types: involuntary and voluntary. Involuntary attention is supported by automatic neural processes, and is particularly evident in implicit memory. Involuntary attention
is activated by a property of the external world — of the stimulus —
and it is captured, according to James, by "big things, bright things,
moving things, or blood." Voluntary attention, on the other
hand, such as paying attention to the road and traffic while driving,
is a specific feature of explicit memory and arises from the internal
need to process stimuli that are not automatically salient. (p. 313)
One
of the key differences between [involuntary and voluntary attention] is
not the absence or presence of salience, but whether the signal of
salience is perceived consciously. Studies also
suggest that, as James had argued, the determining factor in whether
memory is implicit or explicit is the manner in which the attentional
signal for salience is recruited. (pp. 313-314)
In
both types of memory, conversion of short-term to long-term memory
requires the activation of genes, and in each case modulatory
transmitters appear to carry an attentional signal marking the
importance of a stimulus. In response to that signal, genes
are turned on and proteins are produced and sent to all the
synapses. But these signals of salience are called up in
fundamentally different ways for the implicit memory and for the
explicit memory required to form the spatial map in the
mouse.
(p. 314)
In
the implicit memory storage, the attentional signal is recruited
involuntarily (reflexively), from the bottom up: the sensory neurons of
the tail, activated by a shock, act directly on the cells that release
serotonin. In spatial memory, dopamine [a neurotransmitter]
appears to be recruited voluntarily, from the top down: the cerebral
cortex activates the cells that release dopamine, and dopamine
modulates activity in the hippocampus. (p. 314)
The
“presence of salience” is a higher-level form of
what Gregory Bateson called “news of
difference”. In Symbolic Modelling we are always
modelling for “salience” (otherwise known as
‘sorting for significance’).
And in particular “stimuli that are not automatically
salient.” Kandel suggests attending to salient
features is “a determining factor in the conversion of
short-term to long-term memory.” From this we infer
that inviting clients to
voluntarily attend to, and maintain attention
on salient features is a determining factor in encouraging changes that
happen in the session to become long-term memories which are then
involuntarily (i.e. unconsciously) “recruited” when
needed in the future.
This
suggests an important role for us as facilitators. We can pay
attention to what the client finds salient and honour or
“bless” that,
and we can direct attention to
salience that the client pays scant attention to. Some events
and processes that do not automatically recruit voluntary attention are:
3. The role of long-term potentiation
Since
space involves information acquired through several sensory modalities,
it raises the questions: How is the spatial map
established? And, once established, how is it
maintained?
The
spatial map of even a simple locale does not form instantaneously but
over ten to fifteen minutes of the rat's entrance into the new
environment. This suggests that the formation of the map is a
learning process; practice makes perfect also for space.
Under optimal circumstances this map remains stable for weeks or even
months, much like a memory process. (p. 309)
What
is true for rats seems true for many humans too. It often
takes 10-15 minutes for a Clean Space
network to begin to form.
The
first clue to the answers emerged in 1973 when Terje Lomo and Tim Bliss
discovered that the neuronal pathways leading to the hippocampus of
rabbits can be strengthened by a brief burst of neuronal
activity. Lomo and Bliss called this form of synaptic
facilitation long-term potentiation. It soon emerged that
long-term potentiation occurs in all three of the pathways within the
hippocampus and describes a family of slightly different mechanisms,
each of which increases the strength of the synapse in response to
different rates and patterns of stimulation. Moreover there
is a distinction between the processes involved in acquiring the map
(and holding on to it for a few hours) and maintaining the map in
stable form for the long term.
(pp. 282-283 and p. 310)
Key
molecules [are] involved in long-term potentiation. [For
example,] glutamate, a common amino acid, acts on two
different types of receptors in the hippocampus, the AMPA
[alpha-amino-3-hydroxy-5-methylisoxazole-4- propionic acid] receptor
and the NMDA [N-methyl-D-aspartatic acid] receptor. The AMPA
receptor mediates normal synaptic transmission and responds to an
individual action potential in the pre synaptic neuron. The
NMDA receptor, on the other hand, responds only to extraordinarily
rapid trains of stimuli and is required for long-term
potentiation. NMDA receptors can transmit the electrical
signal of the synaptic potential into a biochemical signal. These
biochemical reactions are important because they trigger molecular
signals that can be broadcast throughout the cell and thus contribute
to long-lasting synaptic modifications. (pp. 283-284)
The
analysis of how the NMDA receptor functions showed that it acts as a
coincidence detector. It allows calcium ions to flow through
its channel if and only if it detects the coincidence of two neural
events, one pre synaptic and the other post synaptic. In response to
certain patterns of stimulation, the post synaptic cell also sends a
signal back to the pre synaptic cell calling for more glutamate.
[These] repeated trains of electrical stimulation produce a late phase
of long-term potentiation that lasts for more than a day. (p. 284 and pp. 292-293)
Long-term potentiation involves a self-sustaining feedback loop: a
post
synaptic cell triggers a
pre synaptic cell to produce more glutamate
which triggers the
post synaptic cell and so on. The effect
is long-term memory.
In
Symbolic Modelling the Maturing a Change process may work in a similar
fashion. The repeated “potentiation” of new
symbols, functions or relationships helps to consolidate the changed
Landscape. The above suggests this process would be aided by
facilitating the client to attend to the
reorganised spatial
configuration of symbols or spaces. Ways to do this are:
- Direct questions to any changes in spatial relations, e.g. distance, angle, boundary, etc.
- Ask questions of the changed Landscape which require spatial “cognitive sensibilities”,
e.g.
What’s between X and
Y?
(and other specialised questions about space)
When X
is there, what happens to Y?
What does X know
from there
about Y
over there?
(A Clean Space question which can also be used within a Metaphor Landscape.)
- Physicalise the Landscape and visit different symbols noting their changed spatial relationships and perspectives.
- If a client using Clean Space moves some of their spaces, or discovers
new spaces, at the end of the session the client
can be invited to “walk to each space ... and between the
spaces ... and round the periphery of the spaces ... and notice where each
space is in relation to the other spaces ... and whether the spaces have a
shape or a configuration.”
- 0 - 0 - 0 - 0 -
Other ThoughtsThere are two common ways to do ‘second position’ NLP modelling, i.e. imagine being someone else. Either:
a.
Move your ‘I’ into their body (e.g. Steve Gilligan's ‘deep trance identification’
modelling)
or
b. Move
their ‘I’ into your body (Richard
Bandler’s ‘Teach me how you do you’
modelling).
(a) Sees the external world as relative to the other person’s
body and presumably uses some form of allocentric coordinates.
(b) Maintains the external world relative to your body and therefore uses egocentric coordinates.
And there
is another way to model someone else’s perspective
— the Tompkins and Lawley’s way to model
symbolically as a the clean facilitator:
(c) In
Integral Spirituality, Ken Wilber calls this persepctive the “Outside view of the Inside of another's I” because you imagine what another person is
experiencing from their (Inside) perspective while maintaining your
own (Outside) perspective. We think this is their egocentric
perspective within your allocentric perspective.
To use a metaphor:
(a)
is like sitting in the passenger seat of someone else’s car
while they are driving and mimicking how the car is being driven.
(b) is like driving your own car following instructions from someone else as they tell you how they would drive it.
(c)
is like driving your own car while your Sat Nav is showing you what
someone else is experiencing while they are driving their own
car.
Follow-up articles:'
How the Brain Feels: Emotion and Cognition in Neurolinguitsic Psychotherapy' (2002-2007), Philip Harland's excellent five-part paper available on this web site.
Attending to Salience (2009) Penny and my article goes into some depth on what guides our line of questioning and gives
the session its sense of directional flow.
Pointing to a New Modelling Perspective (2012), my paper which provides a different (and I now think more appropriate) metaphor for the clean facilitator's perspective discussed above.
A Modeller's Perspective (2014) my blog exploring six perspectives for modelling (the three mentioned above and three others).
The Neurobiology of Space - ExercisesThe Developing Group, 4 August, 2007
Three exploratory exercises formed the context for the day.
Exercise 1 - Modelling Spaces- in pairs - 20 minutes each way
Purpose:
For the client to self-model their perception of several ‘physical’ spaces.
For the facilitator to develop their skills at modelling and maintaining a person's attention on spatial information.
Facilitator says:
1. Where do you want to be and where do you want me to be? (Client locates both)
2. What spaces do you notice?
3. Select 3 of those spaces spaces.
4. Facilitate the person to describe the attributes of each of the 3 spaces.
5. And then, what’s the same and what’s different about the 3 spaces?
Things for the facilitator to notice during the exercise:
What kind of places are called 'spaces'?
As we cannot directly perceive space, we have to compute it, what characteristics are used to categorise spaces?
When does a person's description became less external-sensory and more imaginary-metaphorical, e.g.
a) The space up there has a curved shape, with flat surfaces.
b) It seems to have a direction.
c) I can imagine myself standing in that space.
Exercise 2 - Blind Clean Space - in pairs - 30 minutes each way.
Purpose:
Vision dominates our sense of space, so what is our sense of space when we have no sight of the external environment?
1. Represent a desired outcome (=B).
2. Place B where it needs to be.
3. Put on blindfold.
4. Locate starting position (=A).
5. Facilitator marks with a post-it note each space (about 6) visited by the client and in which direction they were facing.
6. At the end the client removes blindfold and notices configuration of spaces.
The words in red below are the changes from the original process described in our article
Clean Space: Modelling human perception through emergence

Exercise 3 - Spaces Between- in pairs - 30 minutes each way.
Acknowledgement:
We designed this activity using a mixture of processes originated by David Grove - Clean Language, Clean Space, Clean Worlds and Emergent Knowledge. Articles on these subjects can be found in the menus on the left of this page.
On your own:
1. Identify a topic of interest or a desired outcome.
Represent it on a piece of paper (label it B).
2. What do you know about that B?
Represent that knowing on another piece of paper. (label it A).
3. Ask yourself six times: And what else do I know about B?
i.e. identify six other knowings and put each of those on separate pieces
of paper
(number them 1 to 6).
You should now have 8 pieces of paper.
With a partner:
NB: This exercise is about the ‘space between’ and not about the content on the paper.
4. Place B where it needs to be.
Place yourself where you need to be in relation to B.
Put A where you are.
Place the six other knowings where they need to be in relation to A and B.
5. Starting at A, visit each space in turn and notice the extent of each space.
(Facilitator to note the client’s words that describe the
space between,
e.g. ‘gap’, ‘shared boundary’, ‘edge’, ‘overlap’, etc.)
6. Return to A and select a space-between.
Identify the attributes of the space-between selected,
e.g.
- And does that ... have a size or a shape? (... is a space between word)
- And what’s on either side of that ...?
- And how far does the ‘overlap’ overlap?
- And how far does ... extend?
- And what’s behind ...?
- And what’s between ... and ...?
7. Select another 'space between' and repeat Step 6 several times
8. End by returning to A and asking:
- And what do you know now?
- And is there anything about these spaces that needs to be different?
If yes (and after they have made the alteration):
- And what do you know now?
© 2007, Penny Tompkins and James Lawley