Conflict and Reorganization

Re: Conflict and
Reorganization
[Martin Taylor 20045.01.18.10.52]

Not responding to any specific post, but several writers in the
“sense of self” thread have referred to reorganization as
being driven by conflict or by persistent error in the control
hierarchy (which conflict assures).

In my view, that’s wrong. Yes, reorganization may be more
probable (happen at a greater rate) when there is persistent error,
but that’s probably a non-causal correlation. The cause of
reorganization is failure of some intrinsic variable to be
maintained near its reference level. It doesn’t matter whether you buy
into the strict HPCT hierarchy or simply into the fundamental notion
that Perceptual Control is the foundation of life, the object of
control is to ensure that the intrinsic variables that keep an
organism alive stay at appropriate levels. What these intrinsic
variables are probably is determined by the organism’s genetic makeup.
Many of them are presumably chemical (enzymes, hormones, etc.,
etc.).

Intrinsic variables are not directly perceived or affected by the
main perceptual control system structure – at least, that’s an
assumption of HPCT, and it’s good enough to work with. They are
influenced by side-effects of perceptual control, and in turn, they
affect the operation of the perceptual control structure, sometimes
directly, as altering the chemical balance can change the behaviour of
the nuerons, some times indirectly as they are presumed to do in
reorganization. That’s their form of control loop.

Reorganization loop

The consistency with which the side-effects of perceptual control
influence particular intrinsic variables will be affected by the
consistency of perceptual control itself. If there is persistent error
in the hierarchy, the way the organism interacts with the world will
usually be less consistent than it would be if control were good. If
there’s persistent error, something has to change, or the side-effects
that influence the intrinsic variables won’t have a consistent
influence.

Organisms that have evolved to force changes in the perceptual
control structure when intrinsic variables deviate from their
reference values are more likely to survive and propagate than are
those that have no such reorganization mechanism. So it would not be
unlikely if evolution had provided some mechanism by which persistent
error in the main hierarchy could be detected, and used as is the
“imagination loop” in the main control hierarchy, as a
surrogate for the real-world effects of actions. Mark Lazare’s 3-D
cube nicely shows such a “pseudo-imagination loop”.

If evolution has produced the ability for the organism to use a
“pseudo-imagination loop”, then yes, reorganization may well
occur at a rate dependent on persistent error in the main control
structure. But its primary driver isn’t likely to be that
“pseudo-imagination loop”. Rather, it will be real
disturbances to the life-preserving intrinsic variables.

Martin

intrinsic.1.gif

[From Bruce Gregory (2005.0118.1155)]

Martin Taylor 20045.01.18.10.52

Not responding to any specific post, but several writers in the "sense
of self" thread have referred to reorganization as being driven by
conflict or by persistent error in the control hierarchy (which
conflict assures).

In my view, that's wrong. Yes, reorganization may be more probable
(happen at a greater rate) when there is persistent error, but that's
probably a non-causal correlation. The cause of reorganization is
failure of some _intrinsic variable_ to be maintained near its
reference level.

Do you have an explanation for changes that do not directly depend on
the failure of some intrinsic variable? For example, I have suggested
how reorganization might play a role in MOL and RTP. You seem to argue
that this is not the mechanism involved. What is? Or would you say that
MOL and RTP are associated with the failure of intrinsic variables to
maintain their reference levels.

The enemy of truth is not error. The enemy of truth is certainty.

[Martin Taylor 2005.01.18.12.41]

[From Bruce Gregory (2005.0118.1155)]

Martin Taylor 20045.01.18.10.52

Not responding to any specific post, but several writers in the "sense
of self" thread have referred to reorganization as being driven by
conflict or by persistent error in the control hierarchy (which
conflict assures).

In my view, that's wrong. Yes, reorganization may be more probable
(happen at a greater rate) when there is persistent error, but that's
probably a non-causal correlation. The cause of reorganization is
failure of some _intrinsic variable_ to be maintained near its
reference level.

Do you have an explanation for changes that do not directly depend on
the failure of some intrinsic variable? For example, I have suggested
how reorganization might play a role in MOL and RTP. You seem to argue
that this is not the mechanism involved. What is? Or would you say that
MOL and RTP are associated with the failure of intrinsic variables to
maintain their reference levels.

I don't have any thoughts on RTP at the moment. As for MOL, I'm not
sure that it involves any reorganization, though it could. One of the
aphorisms that always underlies the PCT hierarchy is that "there are
many ways to skin a cat." More academically, there are potentially
many higher-level control systems supported by any one lower-level
one, and many lower-level systems that support any higher-level one.
If one route to influencing a controlled perception is blocked,
another may become more effective.

There's a general question of choice: does one walk, bicycle, or
drive? Each supports control of the perception of seeing oneself at
the destination. Does it need random reorganization to permit the
choice? Are the unchosen mechanisms delinked from the higher-level
control system? I don't think so.

Likewise with MOL. The question of choice arises, at least if the
person has available another method of controlling one or other of
the conflicted perceptions in such a way as to reduce the conflict.
If they don't then reorganization may well occur. But I don't think
it likely that reorganization can be controlled, or even influenced
by directing attention to the place where the problem exists.

The role of consciousness may be in influencing the switching of
which mechanisms are used to control the higher-level variables. If
so, that would tie in with what I think of as the normal correlate of
conscious attention: places of difficult control and places where
control of one perception may be dropped in faviour of control of
another not currently under direct control.

All of this is truly speculative, as may be obvious to you. But no
more so than a lot of PCT theorizing and less so than most, if one
believes in both PCT and evolution.

Martin

[From Bruce Gregory (2005.0118.1345)]

Martin Taylor 2005.01.18.12.41

There's a general question of choice: does one walk, bicycle, or
drive? Each supports control of the perception of seeing oneself at
the destination. Does it need random reorganization to permit the
choice? Are the unchosen mechanisms delinked from the higher-level
control system? I don't think so.

Of course the simplest explanation is that choice is an invention of
the conscious mind and has nothing to do with the operation of the
hierarchy. When the hierarchy acts, we experience having chosen
something. At least this is consistent with brain scan studies.

Likewise with MOL. The question of choice arises, at least if the
person has available another method of controlling one or other of
the conflicted perceptions in such a way as to reduce the conflict.
If they don't then reorganization may well occur. But I don't think
it likely that reorganization can be controlled, or even influenced
by directing attention to the place where the problem exists.

I agree. But we seem to be a minority on CSGnet. However, conflict can
be created and to the extent that persisting error leads to
reorganization, the latter can be made more likely.

The role of consciousness may be in influencing the switching of
which mechanisms are used to control the higher-level variables. If
so, that would tie in with what I think of as the normal correlate of
conscious attention: places of difficult control and places where
control of one perception may be dropped in faviour of control of
another not currently under direct control.

Again I think consciousness is a red herring as far as hierarchical
control is concerned.

All of this is truly speculative, as may be obvious to you. But no
more so than a lot of PCT theorizing and less so than most, if one
believes in both PCT and evolution.

I agree, so long as you can pull rabbits out hats by invoking a causal
role for consciousness. As far as I am concerned this is a deus ex
machina that we must learn to do without. I'm doing my best.

The enemy of truth is not error. The enemy of truth is certainty.

[From Bill Powers (2005.012.20.1000 MST)]

Martin Taylor 20045.01.18.10.52 –

Yes, reorganization may be more
probable (happen at a greater rate) when there is persistent error, but
that’s probably a non-causal correlation. The cause of reorganization is
failure of some intrinsic variable to be maintained near its reference
level. It doesn’t matter whether you buy into the strict HPCT hierarchy
or simply into the fundamental notion that Perceptual Control is the
foundation of life, the object of control is to ensure that the intrinsic
variables that keep an organism alive stay at appropriate levels. What
these intrinsic variables are probably is determined by the organism’s
genetic makeup. Many of them are presumably chemical (enzymes, hormones,
etc., etc.).

I think this is the basic principle we have to keep in mind – well said.
We’ve discussed the possibility that error signals in learned control
systems might, if extreme enough, be considered as intrinsic variables
with reference levels of zero. If comparators tend to appear as specific
features of the brain, and that seems to be true in at least some places,
it would be possible for excessive signals in those locations to be the
object of intrinsic control via reorganization independently of the
nature of any controlled variable associated with the comparator (and
that would make the development of control systems very much more likely)
My thinking has been subject to the constraint that anything proposed to
be part of the reorganizing system has to be present and working before
any learned systems have been acquired. Otherwise we’d be talking about
acquired processes of learning, not the basic inherited processes
affected by natural selection – that is, what I call “E. coli
reorganization” to distinguish it from other possible
kinds.

I agree that Marc Lazarre’s 3D diagram shows the proper relationship of a
reorganizing system to the hierarchy – it’s not the “highest
level”.

Organisms that have evolved to
force changes in the perceptual control structure when intrinsic
variables deviate from their reference values are more likely to survive
and propagate than are those that have no such reorganization
mechanism.

Yes. Have you read my essay in World Futures along these lines? The basic
trick is to focus on accuracy of replication (not “survival”).
Some environmental variables tend to reduce accuracy of replication when
in certain states (temperature, for example). If a complex molecule
interacts with its substrate in such a way as to reduce the effects of
such disturbing variables, the result will be more accurate replication
– and hence, longer survival of that particular species of molecule.
This negative feedback automatically makes that species more prevalent
than those having no such stabilizing effects on disturbed variables. So
my definition of fitness has nothing to do with population numbers, and
everything to do with controlling aspects of the environment that affect
accuracy of replication. If the survivors become more numerous than the
others, that’s only a side-effect of replicating more accurately. Under
this view, it’s not mutations that are the central puzzling fact, but the
lack of change over long periods of time, which is the result of
controlling the variables that affect change.

Also, of course, E. coli reorganization then becomes just an internalized
version of the evolution of control.

Best,

Bill P.

[From Bill Powers (2005.01.20.1050 MST)]

Bruce Gregory (2005.0118.1345)--

I agree, so long as you can pull rabbits out hats by invoking a causal
role for consciousness. As far as I am concerned this is a deus ex
machina that we must learn to do without. I'm doing my best.

Do you mean that you're consciously doing your best? If consciousness has
no causal role, I would assume that this is NOT what you mean, for then
consciously trying, or not trying, would be irrelevant. What do you mean in
this comment?

Best,

Bill P.

[From Bruce Gregory (2005.0120.1345)]

Bill Powers (2005.01.20.1050 MST)

Bruce Gregory (2005.0118.1345)--

I agree, so long as you can pull rabbits out hats by invoking a causal
role for consciousness. As far as I am concerned this is a deus ex
machina that we must learn to do without. I'm doing my best.

Do you mean that you're consciously doing your best? If consciousness
has
no causal role, I would assume that this is NOT what you mean, for then
consciously trying, or not trying, would be irrelevant. What do you
mean in
this comment?

I am controlling for developing a model of behavior that consists
solely of hierarchically linked ECUs.

The enemy of truth is not error. The enemy of truth is certainty.

[From Bill Powers (2005.01.10.1400 MST)]

Bruce Gregory (2005.0120.1345)--

Do you mean that you're consciously doing your best? If consciousness
has no causal role, I would assume that this is NOT what you mean, for then
consciously trying, or not trying, would be irrelevant. What do you
mean in this comment?

I am controlling for developing a model of behavior that consists
solely of hierarchically linked ECUs.

Yes, but are you doing this consciously? If your controlling for that kind
of model is simply an automatic reaction to disturbances or the
happenstance outcome of random reorganizations, it would not matter whether
you are developing this model consciously or without consciousness. Or,
come to think of it, if you were developing some other model instead. But
if you're conscious of doing this, wouldn't that require some sort of
explanation?

Are you sure you're not just saying that you don't know how put
consciousness into a model? That would be different from saying that
consciousness plays no causal role in anything. To defendc that assertion
would require you to know what consciousness/awareness is, wouldn't it?

Best,

Bill P.

In a message dated 1/20/2005 2:07:56 P.M. US Mountain Standard Time, powers_w@FRONTIER.NET writes:

consciousness/awareness

Is anyone who is reading this thread – also reading MOL - 3D PCT reorganization, awareness and attention…???

I only ask because we are all talking about the same things how to model reorganization consciousness/awareness and attention and how it is related to “acceptable error” “intrinsic error” or larger integration factors as you go up the hierarchy.

image00214.jpg

Sincerely,

Mark A. Lazare, Managing Partner

Compass Mental Health, LLC

4500 N. 32nd Street, Suite 104

Phoenix, AZ 85018

602 224-7050

877 224-7050

http://www.CompassMentalHealth.com/

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[From Erling Jorgensen (2005.01.20 1430 EST)]

Bill Powers (2005.012.20.1000 MST)

We've discussed the possibility that error signals in learned control
systems might, if extreme enough, be considered as intrinsic variables

with

reference levels of zero.

Your comments here speak to an obstacle I have pondered,
in considering whether cumulative error could function as
an intrinsic variable in its own right.

The issue is this: How is an "extreme enough" error signal
different from any other high magnitude or high frequency
signal in the brain? A given signal is only designated an
"error signal" with respect to the entire loop. That term
describes how it functions in a particular _composite_
organization that we call a negative feedback control loop.

Open loop, it is just a signal, same as any other, with a
frequency considered proportional to its net input. To give
it special status at that level of analysis would seem to
make "an error in logical typing", to use Bateson's helpful
phrase.

This is the same issue we encounter with every component of
the control loop. Neurons do not know what a given signal
means. Neural fibers do not know what their signals mean.
Even a reference signal does not know what its corresponding
perception means.

It is the operation of the loop as a whole that makes a
certain signal (one we call "perceptual") track another
signal (one we call "reference"), and all of that happens
without worrying what the signals "mean."

The one place I have specifically wondered about meaning is
the error signal itself. It is very tempting to allow a
basic property at that point, such that more error = "bad"
(by definition!) and less error = "good".

To date, I have considered that a shorthand form of expression,
standing in for a more complicated loop that is actually closed
through the state of the intrinsic variables -- (this is the
corrective that Martin was calling our attention to.) Thus,
the proper definitional formulations would be: intrinsic
error = "bad" and lack of intrinsic error = "good".

There is some clinical use to adopting the shorthand version,
but that is not a proper functional description. However --

My own views on the adaptive function of emotions ties them
to particular changes in (overall?) error in the organism.
For instance, rapidly increasing error seems correlated with
alarm or fear, high sustained error seems correlated with
depression, decreasing error seems correlated with positive
emotions.

Again, I think there is clinical utility in this manner of
description. But trying to get the circuit diagrams to work
this way seemed to introduce additional properties -- what
Bruce G. might call "deus ex machina." And I want to be
very conservative with this matter of functional properties,
whether that be via parameters or other collateral connections.
To my way of thinking, every property should have to earn its
way into the model, with pretty stringent tests.

Getting back to the matter of error signals and emotion --
Basically, I could never get past the problem of logical typing,
to see whether there was any merit in taking such ideas about
emotion any further. Your remarks in this post suggest one
possible route around that problem. Specifically --

If comparators tend to appear as specific
features of the brain, and that seems to be true in at least some

places,

it would be possible for excessive signals in those locations to be the
object of intrinsic control via reorganization independently of the

nature

of any controlled variable associated with the comparator (and that

would

make the development of control systems very much more likely)

This would make error signals distinctive (as signals) by virtue
of their "location", or the "type of structure" functioning as
the comparators. That is a very tempting offer. Too tempting,
to let it slip in unexamined.

Can you say more about the evidence for comparators being
"specific features,... at least in some places"?

Doesn't this introduce an additional property (ripe for
exploitation!) into the model? What data does this allow
for, that are not already adequately handled by the proposal
of an intrinsic system controlling critical chemical
variables?

If "excessive error signals" are the issue, would we be
better off looking downstream to output signals thereby
being driven to maximum levels, which (if sustained)
then become maladaptive to the organism? (This is the
way I currently think of Selye's General Adaption Syndrome
as operating.)

Should we envision (read, predict) that large neural
signals representing excessive error have as a side effect
some kind of spreading chemical toxicity, which turns
them into critical intrinsic variables?

I guess there are any number of ways such signals could
become intrinsic, _IF_ we open the door at all. I just
want us to examine that feature thoroughly, before it
becomes a weight-bearing wall in the model.

All the best,
Erling

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[From Bruce Gregory (2005.0120.2010)]

Bill Powers (2005.01.10.1400 MST)

Bruce Gregory (2005.0120.1345)--

Do you mean that you're consciously doing your best? If consciousness
has no causal role, I would assume that this is NOT what you mean,
for then
consciously trying, or not trying, would be irrelevant. What do you
mean in this comment?

I am controlling for developing a model of behavior that consists
solely of hierarchically linked ECUs.

Yes, but are you doing this consciously? If your controlling for that
kind
of model is simply an automatic reaction to disturbances or the
happenstance outcome of random reorganizations, it would not matter
whether
you are developing this model consciously or without consciousness. Or,
come to think of it, if you were developing some other model instead.
But
if you're conscious of doing this, wouldn't that require some sort of
explanation?

The model is not intended to explain consciousness.

Are you sure you're not just saying that you don't know how put
consciousness into a model? That would be different from saying that
consciousness plays no causal role in anything. To defendc that
assertion
would require you to know what consciousness/awareness is, wouldn't it?

Until I take the model seriously, I have no way of knowing its
limitations.

The enemy of truth is not error. The enemy of truth is certainty.

[From Bill Powers (2005.01.21.0715 MNST)]

Erling Jorgensen (2005.01.20 1430 EST)]

Your comments here speak to an
obstacle I have pondered,

in considering whether cumulative error could function as

an intrinsic variable in its own right.

Do you really mean “cumulative” error? For error to accumulate,
there must be an integrator to accumulate it. In a control system with an
integrating output function, the error itself does not accumulate, but
the output represents the cumulative effect of the
error.

The issue is this: How is
an “extreme enough” error signal

different from any other high magnitude or high frequency

signal in the brain?

It isn’t different as far as I know. It’s just a large signal. But
because it’s generated by comparing a perceptual signal with a reference
signal in a control system, its meaning is that control is not working
very well. That is not the meaning of any other large signal in the loop.
A large perceptual signal means only that the perceived variable is in
the upper part of its range; a large output signal indicates that a lot
of output is being generated, presumably being required to make the
perceptual signal match the reference signal (nearly). In either case,
control can be perfectly normal. But when the error signal is large,
control is not normal.

A given signal is only
designated an “error signal” with respect to the entire
loop. That term describes how it functions in a particular
composite organization that we call a negative feedback control
loop.

Open loop, it is just a signal, same as any other, with a

frequency considered proportional to its net input. To give

it special status at that level of analysis would seem to

make “an error in logical typing”, to use Bateson’s
helpful

phrase.

I see what you mean. But let’s consider the alternative. Suppose
reorganization were caused by any large signal, wherever in the
loop it appeared. This would mean that, for example, extending your arm
fully would cause reorganization to occur (or flexing it all the way, if
maximum joint angle signal is generated by flexion). Thus any control
system that could move the arm to one extreme position would have its
organization changed until it could no longer do that. If avoiding that
extreme position had a positive effect on fitness, this would be a good
thing, but the opposite is more probable. The only signal that
always indicates less-than-perfect control is the error signal.
And in normal systems, error signals are always coming and going –
they’re necessary for producing actions. Therefore reorganization
shouldn’t be started by ordinary levels of error, or should proceed only
slowly for small errors.

The upshot is that if any unusually large signal in the hierarchy of
control systems might give rise to reorganization, it would be the error
signal and not the perceptual signal or the output signal.

The one place I have
specifically wondered about meaning is

the error signal itself. It is very tempting to allow a

basic property at that point, such that more error =
“bad”

(by definition!) and less error = “good”.

Slow down a bit. What is special about an error signal is not the signal,
but the way it is derived. All that a comparator has to do is subtract
the magnitude of one input from the magnitude of another and generate an
output proportional in magnitude to the difference between the input
magnitudes. In principle, all comparators are therefore alike. The
comparator is the only function in the loop of which this is
true.
One requirement I have placed on intrinsic control systems is that they
be inheritable. The reason for this is that to get the hierarchy started
from scratch, there must be a reorganizing system in place and
functioning before any hierarchical systems exist. If some hierarchical
systems are also inherited, that just makes the task of the reorganizing
system easier; I was trying to handle the worst case and show that the
hierarchy could still come into existence.
So we have to imagine a separate inherited system that has evolved to
monitor the states of many physiological and biochemical systems – many,
but not all since that would be impossible. This inherited system has a
built-in set of reference signals (perhaps existing as thresholds of
detection) that specify some “best” state of each intrinsic
variable. The sum of all error signals drives reorganization, a process
that changes synaptic weightings (in a way similar to the E. coli method
of gradient-climbing).
So which variables would this system monitor? Those on which
fitness directly or even indirectly depends. We know that some of these
variables would be (or be affected by) CO2 or glucose concentration in
the bloodstream, or core temperature, or the concentration of lactic
acid, or many other aspects that bear on the life support systems of the
body (including reproductive systems). But now, in the light of the
above, we can suspect that some, but not all, neural signals in the
learned hierarchy would also be monitored: namely, error signals. That’s
the only type of signal that is a reliable indicator of how well any
control system is operating, regardless of what it is controlling.
So if it were possible for an inherited reorganizing system to know which
signals were going to be error signals, error signals could function as
intrinsic variables with respect to the reorganizing system. Is that
possible? I think it is, because as I said above all comparators are
alike, and therefore can be built into the brain even before there are
any control systems. If comparators can be built in, the reorganizing
system can have inherited connections to comparators that detect their
outputs. And that means that large errors can cause reorganization even
if large signals of other kinds can’t.
Why not just say that the reorganizing system acts to reorganize the
control system where the error is? The simple answer is because that’s
not enough to account for all the kinds of learning we see. My stock
example is the bird that learns to walk in a figure-eight pattern to
cause food to appear. There is no logical connection between the way you
walk and what you eat, yet most higher organisms can learn this kind of
connection. I’m pretty sure I could, and I know that pigeons can. It has
to be possible for an intrinsic error to cause reorganization in
any control system.

That’s the general idea I’ve been exploring, and testing, with my
multiple-control-system model. Take 500 control systems controlling 500
different aspects of an environment containing 500 variables. Give each
control system a randomly-selected reference signal value, and an
integrating output function that affects all 500 environmental variables
through a set of random weightings. Let each control system perceive a
variable derived by applying random weightings to each of the 500
environmental variables.

Now let each control system’s input function be reorganized according to
the magnitude of its error signal, using the E. coli method. Result: the
input functions become more and more orthogonal to each other, and the
matrix of input weights for each system approaches the transpose of the
matrix of output weights for each system. This shows that random
reorganization can lead to systematic independent control – if each
control system reorganizes separately. Trying to make them all reorganize
according to the global total error does not work anywhere near as fast,
if indeed it works at all (I can’t tell yet). This says that we need
something to direct reorganization to the systems where the error is. I
sort of knew this, intuitively, but now I can prove it.

At present, the only thing I know of that can focus on systems with error
is attention. So, in an intuitive leap, I have guessed that the function
of attention (central awareness of specific control processes) is to
direct reorganization. If you attend too closely to any skilled
control action, it tends to get disorganized. If there is a problem with
control, attention focuses on the systems with the largest error, and
they begin to reorganize.

What is attention, or awareness? I don’t know. I suspect that it’s the
input function of a system that isn’t part of the hierarchy proper, that
is inherited, and that is capable (when coupled to some
“volitional” output function) of altering both signals and
synaptic weights in other parts of the brain. It may have something to do
with the reticular formation, but that’s a low-quality guess.

My own views on the adaptive
function of emotions ties them

to particular changes in (overall?) error in the organism.

For instance, rapidly increasing error seems correlated with

alarm or fear, high sustained error seems correlated with

depression, decreasing error seems correlated with positive

emotions.

I agree. But this doesn’t imply that emotions are something separate. The
same relationships would be seen if emotions were just the experience of
errors together with the sensations of getting prepared to deal with
them. The idea that emotions are causal or directive is
unnecessary

Again, I think there is clinical
utility in this manner of

description. But trying to get the circuit diagrams to work

this way seemed to introduce additional properties – what

Bruce G. might call “deus ex machina.”

Why “deus”? Why not just “thingy?” Something is quite
obviously “ex” the “machina” as we now conceive it,
but I doubt very much that it’s supernatural or mystical in nature. I
don’t see any problem with designing a system that monitors variables and
acts by altering synaptic connections. The problem isn’t that this is
hard to do, it’s that there are too many ways to do it and we have no
reason to pick one over another, not yet. You tell me what you want a
circuit to do and I’ll give you three circuits that will do it. The hard
part is deciding what you want it to do. Anyone who has designed circuits
for a living will tell you that.

Can you say more about the
evidence for comparators being

“specific features,… at least in some
places”?

The basic specific feature is that a comparator receives one signal that
originates lower in the afferent tree and subtracts it from (or from it)
a signal that originates higher in the efferent tree (afferent = inbound,
efferent = outbound). In the brain stem, cells in the olivary nucleus
receive excitatory collaterals from the sensory pathways, and inhibitory
efferent snals from nuclei of the cerebellum and other sources. These
cells form a layer in the outer part of the nucleus, so all incoming
signals have to pass through it.As a result, the rest of the nucleus is
actuated by a large set of error signals, and the layer is a layer of
comparators. I’m sure there are many other examples at this and higher
levels. And of course, the motor cells of the spinal cord are all
comparators.

If “excessive error
signals” are the issue, would we be

better off looking downstream to output signals thereby

being driven to maximum levels, which (if sustained)

then become maladaptive to the organism? (This is the

way I currently think of Selye’s General Adaption Syndrome

as operating.)

Yes, that’s a good idea if applied carefully. I don’t think we would want
large output signals to cause reorganization in general, because a large
output signal means only that there is a large disturbance. If we
reorganized away the ability to produce large output signals, we would
lose the ability to resist large disturbances. But chronic large
outputs, and more particularly the drain on resources and the incipient
injury that accompanies them, should be good candidates for intrinsic
variables associated with reorganization.

Should we envision (read,
predict) that large neural

signals representing excessive error have as a side effect

some kind of spreading chemical toxicity, which turns

them into critical intrinsic variables?

I favor that idea, maybe because it’s already built in to the theory of
reorganization.

I guess there are any number of
ways such signals could

become intrinsic, IF we open the door at all. I just

want us to examine that feature thoroughly, before it

becomes a weight-bearing wall in the model.

The main thing is that sensing of intrinsic variables should be
inheritable, not brought about by events of a single lifetime. This all
has to work before there are any (or many) higher-order
systems.

And we shouldn’t forget that there are probably other means of
reorganization that are learned: control by changing parameters as
opposed to changing reference signals is certainly a means of
reorganization, and can be acquired. I think the main thing is to avoid
introducing new features into the model until we’re sure that the
existing structure can’t handle some phenomenon. If one gives up too soon
on finding an explanation within the structure we have, the whole
modeling process will lose its discipline. The idea is to introduce new
properties only when you MUST. Not just to be creative.

Best,

Bill P.

[From Bruce Gregory (2005.0121.1140)]

Bill Powers (2005.01.21.0715 MNST)

At present, the only thing I know of that can focus on systems with
error is attention. So, in an intuitive leap, I have guessed that the
function of attention (central awareness of specific control
processes) is to direct reorganization. If you attend too closely to
any skilled control action, it tends to get disorganized. If there is
a problem with control, attention focuses on the systems with the
largest error, and they begin to reorganize.

It seems to me to be quite a leap to associate a system that monitors
error with attention. Attention does not seem necessary to initiate
reorganization (which can go on without conscious awareness), nor does
paying attention to something seem to lead to reorganization in most
cases.

What is attention, or awareness? I don't know. I suspect that it's
the input function of a system that isn't part of the hierarchy
proper, that is inherited, and that is capable (when coupled to some
"volitional" output function) of altering both signals and synaptic
weights in other parts of the brain. It may have something to do with
the reticular formation, but that's a low-quality guess.

The problem I have with this suggestion is that it seems to put all the
intelligence in this system. How does awareness "know" what to change?
What does it mean to be a "volitional output function"?

Again, I think there is clinical utility in this manner of
description. But trying to get the circuit diagrams to work
this way seemed to introduce additional properties -- what
Bruce G. might call "deus ex machina."

Why "deus"? Why not just "thingy?" Something is quite obviously "ex"
the "machina" as we now conceive it, but I doubt very much that it's
supernatural or mystical in nature. I don't see any problem with
designing a system that monitors variables and acts by altering
synaptic connections.

It is a a "deus" if it acts intelligently. If it simply initiates
reorganization whenever it detects persistent error it is a "thingy"--
the reorganization subsystem. It controls for minimizing the perception
of error in other systems and its output consists of random changes to
the organization of those systems.

And we shouldn't forget that there are probably other means of
reorganization that are learned: control by changing parameters as
opposed to changing reference signals is certainly a means of
reorganization, and can be acquired.

I'm not sure I know what "parameters' are in your view. Could you give
a few examples/

I think the main thing is to avoid introducing new features into the
model until we're sure that the existing structure can't handle some
phenomenon. If one gives up too soon on finding an explanation within
the structure we have, the whole modeling process will lose its
discipline. The idea is to introduce new properties only when you
MUST. Not just to be creative.

Amen.

The enemy of truth is not error. The enemy of truth is certainty.

[From Bill Powers n(2005.01.21.1040 MST)]

Bruce Gregory (2005.0121.1140)–

At
present, the only thing I know of that can focus on systems with

error is attention. So, in an intuitive leap, I have guessed that
the

function of attention (central awareness of specific control

processes) is to direct reorganization.

It seems to me to be quite a
leap to associate a system that monitors

error with attention. Attention does not seem necessary to initiate

reorganization (which can go on without conscious awareness), nor
does

paying attention to something seem to lead to reorganization in
most

cases.

It’s a leap, as I said. What “quite” a leap adds to that is not
clear. I did not say that attention is necessary to initiate
reorganization; that is still the role of intrinsic error. What I said
was that attention might be a means of directing the reorganizing process
to the systems in which error exists. I trust that you don’t deny that
when intrinsic errors exist, our attention tends to focus on them. Just
think about trying to attend to a scientific lecture when your bladder is
full.

The problem I have with this
suggestion is that it seems to put all the

intelligence in this system. How does awareness “know” what to
change?

What does it mean to be a “volitional output
function”?

What, all the intelligence? I don’t recall saying that attention
can, for example, speak English or solve equations. The ability to detect
error signals (or whatever indicates the presence of error) is surely not
to be equated with “intelligence.” Though I see nothing wrong
with attributing intelligence to brain operations. Maybe the word
intelligence has some special meaning for you – to me, intelligence
means complex brain operations. Is it something else for you?

Why
“deus”? Why not just “thingy?” Something is quite
obviously “ex”

the “machina” as we now conceive it, but I doubt very much that
it’s

supernatural or mystical in nature. I don’t see any problem with

designing a system that monitors variables and acts by altering

synaptic connections.

It is a a “deus” if it acts intelligently.

That’s a pretty extreme position. Are you saying that there is nothing in
the brain that exhibits intelligence? It seems to me that such a proposal
would be self-defeating. It would say, for example, that the statement
“It is a 'deus’if it acts intelligently” was not the product of
intelligence. Do you want to admit to that?

If it simply initiates
reorganization whenever it detects persistent error it is a
“thingy”-- the reorganization subsystem. It controls for
minimizing the perception of error in other systems and its output
consists of random changes to the organization of those
systems.

Yes, but what makes sure it is directed to act on the part of the brain
that is associated with the error instead of some other part that is
working properly? Something has to be “intelligent” enough to
localize the effects of reorganization. I take it that you wouldn’t
recommend that we have ten billion reorganizing systems which act to
reorganize every brain cell, which is the alternative to an ability to
detect error signals and direct the effects of reorganization
accordingly. And anyway, that wouldn’t handle learning to walk in a
figure eight to get fed.

I’m not sure I know what
"parameters’ are in your view. Could you give

a few examples.

In a model of a control system, the parameters are the parts of the
system that remain the same, in contrast to the signals, which vary. In
the describing equations, the parameters are the constants. Suppose we
have a function

Y = A1X1 + A2X2 + … An*Xn

The parameters of this function are the coefficients A1, A2, … An.
Reorganization would consist of changing the values of those coefficients
(remembering that one possible value of a coefficient is zero, indicating
that the corresponding input has no effect on the output). Control by
parameters would consist of controlling by altering one or more of these
coefficients. “Hebbian learning,” as far as I can see, consists
of altering parameters.

Best,

Bill P.

[From Bruce Gregory (2005.0121.1353)]

Bill Powers (2005.01.21.1040 MST)

Bruce Gregory (2005.0121.1140)--

At present, the only thing I know of that can focus on systems with
error is attention. So, in an intuitive leap, I have guessed that the
function of attention (central awareness of specific control
processes) is to direct reorganization.

It seems to me to be quite a leap to associate a system that monitors
error with attention. Attention does not seem necessary to initiate
reorganization (which can go on without conscious awareness), nor does
paying attention to something seem to lead to reorganization in most
cases.

It's a leap, as I said. What "quite" a leap adds to that is not clear. I did not say that attention is necessary to initiate reorganization; that is still the role of intrinsic error. What I said was that attention might be a means of directing the reorganizing process to the systems in which error exists. I trust that you don't deny that when intrinsic errors exist, our attention tends to focus on them. Just think about trying to attend to a scientific lecture when your bladder is full.

The fact that you aware when your bladder is full is interesting, but unrelated to the operation of the model, as far as I can tell. I am interested in what the model predicts, not what I experience that the model does not predict.

The problem I have with this suggestion is that it seems to put all the
intelligence in this system. How does awareness "know" what to change?
What does it mean to be a "volitional output function"?

What, all the intelligence? I don't recall saying that attention can, for example, speak English or solve equations. The ability to detect error signals (or whatever indicates the presence of error) is surely not to be equated with "intelligence." Though I see nothing wrong with attributing intelligence to brain operations. Maybe the word intelligence has some special meaning for you -- to me, intelligence means complex brain operations. Is it something else for you?

If the system "knows" what to do other than initiating reorganization in the system experiencing persistent error, it is a black box with intelligence, in my view. If awareness "knows" that it wants to switching from controlling one perception to controlling another perception, then it is intelligent. A thermostatically controlled furnace relies on an outside agent to determine its goals. I am trying to model an autonomous system that does not require the existence of such outside agents. I though you were, too.

Why "deus"? Why not just "thingy?" Something is quite obviously "ex"
the "machina" as we now conceive it, but I doubt very much that it's
supernatural or mystical in nature. I don't see any problem with
designing a system that monitors variables and acts by altering
synaptic connections.

It is a a "deus" if it acts intelligently.

That's a pretty extreme position. Are you saying that there is nothing in the brain that exhibits intelligence? It seems to me that such a proposal would be self-defeating. It would say, for example, that the statement "It is a 'deus'if it acts intelligently" was not the product of intelligence. Do you want to admit to that?

If it simply initiates reorganization whenever it detects persistent error it is a "thingy"-- the reorganization subsystem. It controls for minimizing the perception of error in other systems and its output consists of random changes to the organization of those systems.

Yes, but what makes sure it is directed to act on the part of the brain that is associated with the error instead of some other part that is working properly? Something has to be "intelligent" enough to localize the effects of reorganization. I take it that you wouldn't recommend that we have ten billion reorganizing systems which act to reorganize every brain cell, which is the alternative to an ability to detect error signals and direct the effects of reorganization accordingly. And anyway, that wouldn't handle learning to walk in a figure eight to get fed.

Of course. I never suggested otherwise. In fact I stated explicitly that the system must initiate reorganization in the subsystem that is experiencing persistent error.

I'm not sure I know what "parameters' are in your view. Could you give
a few examples.

In a model of a control system, the parameters are the parts of the system that remain the same, in contrast to the signals, which vary. In the describing equations, the parameters are the constants. Suppose we have a function

Y = A1*X1 + A2*X2 + ... An*Xn

The parameters of this function are the coefficients A1, A2, ... An. Reorganization would consist of changing the values of those coefficients (remembering that one possible value of a coefficient is zero, indicating that the corresponding input has no effect on the output). Control by parameters would consist of controlling by altering one or more of these coefficients. "Hebbian learning," as far as I can see, consists of altering parameters.

If control is successful, however it is achieved, reorganization is unnecessary and will not occur. Reorganization can alter parameters at random as well as altering reference levels at random, I would think.

The enemy of truth is not error. The enemy of truth is certainty.

[From Erling Jorgensen (2005.01.21 1310 EST)]

Bill Powers (2005.01.21.0715 MNST)

Erling Jorgensen (2005.01.20 1430 EST)

Very helpful post, Bill.

Do you really mean “cumulative” error? For error to accumulate,
there must be an integrator to accumulate it.

Sloppy language on my part. I meant something more like “composite”
error or “global” error in the system at a given point in time.
At least that would be my first-pass approximation. Your post
goes on to describe monitoring error (and thus, directing
reorganization) at a much more local level. That’s a feature
I have been interested in, too. But I have wanted to move toward
it cautiously – i.e., because we “must” add it to the model, not
because we “can”.

The issue is this: How is an “extreme enough” error signal
different from any other high magnitude or high frequency
signal in the brain?

It isn’t different as far as I know. It’s just a large signal.
…its meaning is that control is not working very well.

Yes, this is my point. And “meaning” here is a function, not
of a particular segment or signal in the loop, but of how it
functions in the loop as a whole. As I said, “error” (per se)
is at a different logical level of analysis.

But your remarks remind me that error is a unique statement
about the state of control, at that composite level of analysis.
I had forgotten that large error is not needed to derive
large output (to counteract the effects of large disturbance).
We have a gain parameter, which if high enough, can derive large
outputs from even a small amount of error.

And that means, as you go on to point out, that we have a
signal uniquely situated to improve the efficiency of
reorganization – without any need for “intelligent” agency
as to the content of what particular errors represent.

But let’s consider the alternative. Suppose reorganization
were caused by any large signal, wherever in the loop it
appeared… Thus any control system that could move the
arm to one extreme position would have its organization
changed until it could no longer do that.

I agree, this is not a viable alternative. And if evolution
had attempted it, it likely would have been deselected (by
lack of survival) or reorganized away. Control systems need
the ability to counteract the perceptual effects of large
disturbances.

Therefore reorganization shouldn’t be started by ordinary
levels of error, or should proceed only slowly for small
errors.

Yes, and presumably slow integrators or threshold parameters
would be ways to simulate that requirement in a model. Let’s
also not forget Martin’s suggestion – maybe error shouldn’t
trigger any reorganization, until other intrinsic variables
are affected.

All that a comparator has to do is subtract the magnitude of
one input from the magnitude of another and generate an output
proportional in magnitude to the difference between the input
magnitudes.

Yes, that is the core feature of comparators, (together with
an additional feature that you mention later.) My problem
with that (until I read later in your post) was that all sorts
of neurons get both excitatory and inhibitory input, and
generate output proportional to the difference. I don’t think
every neuron is functioning as a comparator. That’s where
your additional feature from later in your post comes in –

The basic specific feature is that a comparator receives
one signal that originates lower in the afferent tree and
subtracts it from (or from it) a signal that originates
higher in the efferent tree (afferent = inbound, efferent =
outbound).

Outbound minus inbound (or vice versa), that would seem to
be the key. With that caveat, I think your (earlier)
statement is now correct –

In principle, all comparators are therefore alike. The
comparator is the only function in the loop of which this
is true.

And for us to capitalize on that feature (say, with some
kind of error-monitoring system), it has to be true of
the neuro-anatomy, too – at least in a broad functional
sense.

So the question is, is there something about neural
development that allows certain neurons or ganglia of
neurons to differentiate inbound from outbound? The
prediction of HPCT would be “yes”, if we indeed allow
this feature of comparators to do some of the heavy
lifting, with a meta-monitoring system.

In the brain stem, cells in the olivary nucleus receive
excitatory collaterals from the sensory pathways, and
inhibitory efferent snals from nuclei of the cerebellum
and other sources… the layer is a layer of comparators.
… And of course, the motor cells of the spinal cord are
all comparators.

These are useful anatomical examples from the developed
nervous system. They do not address the inheritabililty
requirement, for how they might have developed. As you
say –

One requirement I have placed on intrinsic control systems
is that they be inheritable. The reason for this is that
to get the hierarchy started from scratch, there must be a
reorganizing system in place and functioning before any
hierarchical systems exist.

So, to specify the prediction a bit finer: In the developing
nervous system, there would need to be local indicators
(perhaps controlled chemical variables?) such that the
structures that become comparators receive at least one
input each from the collaterals that later are seen to
originate in efferent and afferent pathways, respectively.
If that prediction is borne out by subsequent discoveries,
we should have no problem retaining this aspect of the
model that we are in the process of devising… <:->

The core of the argument is this, with emphasis on the if
it were possible
:

So if it were possible for an inherited reorganizing system
to know which signals were going to be error signals, error
signals could function as intrinsic variables with respect
to the reorganizing system… If comparators can be built in,
the reorganizing system can have inherited connections to
comparators that detect their outputs. And that means that
large errors can cause reorganization even if large signals
of other kinds can’t.

A lot hinges on the uniqueness of comparators, (recognizable
to a developing nervous system, controlling something about
the local environment without recourse to “intelligent
overview”). That is why your statements about comparators in
your earlier post leaped out at me.

Why not just say that the reorganizing system acts to
reorganize the control system where the error is? The
simple answer is because that’s not enough to account for
all the kinds of learning we see. My stock example is
the bird… [etc.]

The other answer is that the phrase “where is the error is”
is exceedingly ambiguous. Error is a property of loops,
(primarily). So where on the loop should the reorganization
be directed? There’s a sensory portion, and a CNS portion,
and a motor output portion, and an environmental feedback
portion. Moreover, every higher level variable includes
a good portion of the lower levels to complete its loop.
It is tempting to call it a “virtual loop”, just to
emphasize this hierarchical feature – but, of course, its
connections are just as real, no matter how many other
loops it incorporates into its path.

Now in this discussion, we are starting to make error a
property of a specific location – i.e., whatever emerges
from an identifiable comparator. But I don’t think we want
reorganization targeted there, because a net change of
sign (inserting an inhibitory interneurone?) might lose
us negative feedback itself.

Your multiple-control-system model is a fascinating
exploration of one place to target the reorganization –
‘let’s make it the input function’.

I agree with your first conclusion, what I would call a
proof of principle –

Result: the input functions become more and more
orthogonal to each other… This shows that random
reorganization can lead to systematic independent
control – if each control system reorganizes separately.

This is quite a demonstration. “Systematic” can emerge
from what is “random”. It maybe implies, in passing,
that randomness is not something to fear – it does not
mean random outcomes, just random attempts.

The second thing I am struck by is the orthogonal aspect
itself. It seems that one way for each reorganizing
control system to minimize the effects of disturbances
from all the other controlling systems is to, in effect,
create maximal distance for itself in the perceptual
state space. We could say it creates a perceptual niche(!),
in which conflict with other control systems is minimized.
This seems to me an extremely significant finding.

I am further intrigued by the matrices you describe.

the matrix of input weights for each system approaches
the transpose of the matrix of output weights for each
system.

Would the transpose still happen if the outputs could
only affect a subset of the 500 environmental variables
(say, 200 or 300)? [I’m not sure if that would allow enough degrees of freedom for stable control to be established.] I have this vague image of the weightings
being mirror images, and am wondering if there is any
artifact coming from each system being derived from and
affecting all 500 variables. I probably do not understand
enough about transpose matrices, to even raise the
question. (When I ran a version of your simulation
on-line sometime last year, I got a little confused
about how to understand what was happening.)

More to the point, in the present discussion, is your
finding about localized reorganization –

…if each control system reorganizes separately. Trying
to make them all reorganize according to the global total
error does not work anywhere near as fast, if indeed it
works at all (I can’t tell yet). This says that we need
something to direct reorganization to the systems where
the error is.

This suggests there might be a decided evolutionary
advantage to such directed reorganization. Such that –
if it arose, it would tend to persist.

I also take this as one form of evidence, addressing my
earlier reservation –

Doesn’t this introduce an additional property (ripe for
exploitation!) into the model? What data does this allow
for,…?

You’ve inserted a single (and plausible) constraint –
let reorganization specifically affect “input functions
…according to the magnitude of [the control system’s]
error signal”. What emerges, in this demonstration,
are orthogonal perceptual niches. That is a very
intriguing finding.

At present, the only thing I know of that can focus on
systems with error is attention. So, in an intuitive leap,
I have guessed that the function of attention (central
awareness of specific control processes) is to direct
reorganization.

I have been guessing that emotion might play this role.
But I think your evidence may be better than mine. –

If you attend too closely to any skilled control action,
it tends to get disorganized. If there is a problem with
control, attention focuses on the systems with the largest
error, and they begin to reorganize.

Experientially, at least in general terms, this seems to
be true. Whereas I do not think we could make a similar
first-approximation generalization to situations associated
with emotion.

I still think there is some kind of semi-hard-wired
association between different emotions and the rate of
change of error (whether global or local, I’m not sure.)
And I note your cautions, such that –

The same relationships would be seen if emotions were just
the experience of errors together with the sensations of
getting prepared to deal with them. The idea that emotions
are causal or directive is unnecessary.

I agree there is no necessity. And I agree with you (and
James and Lange) that a big part includes the body’s “sensations
of getting ready to deal with” errors.

What I wonder about is the apparent “experience of errors” part.
With everything else, according to the postulates of PCT,
we only experience “perceptions.” And yet, here, when it comes
to emotion, I believe there is a more direct experience of
changing errors. This might be an illusion. It might all be
mediated through various kinds of proprioception. Or it
might be the one place where we experience more than our
perceptual inputs.

If so, if this latter intuition is possible, what might be
the evolutionary reason for such an arrangement? Is there
some kind of functional advantage, that would not mess up
a hierarchy functioning well in other respects?

My suspicion is that emotion might involve some kind of
reversible amplification feature. Driving the reorganization
of the intrinsic system is just not plausible, because (as
you note) that has to work prior to the appearance of the
hierarchy, to make the hierarchy appear in the first place.

And your intuition about awareness is a better candidate, for
most reorganization that does not explicitly channel through
the intrinsic hierarchy. Perhaps emotion has something to
do with your category of “learned reorganization”…

And we shouldn’t forget that there are probably other means
of reorganization that are learned: control by changing
parameters as opposed to changing reference signals is
certainly a means of reorganization, and can be acquired.

Some of my explorations in the past have certainly gone the
route of how the “gain” parameter might be adjusted, and
whether emotion might be tied in with that. That resonates
intuitively for me with both positive and negative emotions
– akin to “tuning up or tuning down” our responsivity in
different situations.

I whole-heartedly agree with your parting comments –

I think the main thing is to avoid introducing new features
into the model until we’re sure that the existing structure
can’t handle some phenomenon.

I think this methodological constraint has resulted in some
frustration for those who are looking for greater isomorphism
between the model and a) neurophysiological features on the
one hand, and b) phenomenological experiences on the other.
But the model does not have to look right, it has to act
right. And it has to do that generatively, without adding
ad hoc connections just to make a specific behavior turn
out right.

It’s easy to forget that the model is supposed to be a
lean pared-down functional diagram of only those connections
that are absolutely necessary. As you say –

The idea is to introduce new properties only when you MUST.
Not just to be creative.

Thanks for your detailed response. I hope these remarks
are comparably helpful.

All the best,
Erling

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<<<>>>

[From Dick Robertson, 2005.01.21.1955CST]

···

From: Bill Powers <powers_w@FRONTIER.NET>
Date: Friday, January 21, 2005 12:11 pm
Subject: Re: Conflict and Reorganization

[From Bill Powers n(2005.01.21.1040 MST)]

Bruce Gregory (2005.0121.1140)--

>> At present, the only thing I know of that can

focus on systems

>>error is attention. So, in an intuitive

leap, I have guessed

that the
>>function of attention (central awareness of

specific control

>>processes) is to direct reorganization.

This idea is a surprise to me. It seems you are
saying that attention can be some sort of active
agent. I thought only control systems are active
agents in your theory. From your remarks about the
observer I have always assumed that you, too, viewed
attention/consciousness/awareness as some form of
observation of what's going on when control systems
are controlling.

Best,

Dick R

[From Bill Powers (2005.01.21.1907 MST)]

Dick Robertson, 2005.01.21.1955CST--

This idea is a surprise to me. It seems you are
saying that attention can be some sort of active
agent. I thought only control systems are active
agents in your theory. From your remarks about the
observer I have always assumed that you, too, viewed
attention/consciousness/awareness as some form of
observation of what's going on when control systems
are controlling.

Yes, but we also have to acknowledge the seeming need to focus
reorganization where it's needed. Control systems control; the reorganizing
system reorganizes, and -- the proposal is -- awareness aims reorganization.

I don't think we can ignore the phenomena of consciousness just because the
control model doesn't explain them. Consciousness exists; control exists;
what is the relationship between them? Is there a volitional side of pure
observation? That is, can we voluntarily cause signals to appear in the
hierarchy just by shifting attention? I think we can. What's wrong with
admitting that? The worst thing that can result is that we might have to
add something to PCT. Isn't that to be expected?

An interesting phenomenon arises in eye movement research. While foveating
a target, one can attend elsewhere in the visual field, so that later the
direction of gaze will jump to the direction of the selected off-axis
target (within 2 degrees). This is easy to try out. Look at something, then
without moving the eyes change the focus of attention to some other object
in the visual field. Then look at it -- the image will be centered in one
very rapid movement (possibly followed by one or two small corrections).

So what is the effect of this process we call attending in this experiment?
Clearly it establishes a reference direction of gaze which the succeeding
eye movement will bring about. So attending is not simply passive
observation. It also selects a target for a control action, a process which
has definite physical effects. Attending moves the focus of awareness
around within the visual field, without any eye movement. No behavior is
produced. Yet the control systems have been affected, for when the next
control action takes place, it will control for looking at the selected
object, as the next saccade will show.

Clearly, moving the focus of observation affects actions. Attending has
physical effects. Consciousness and awareness have physical effects in the
brain.

Best,

Bill P.

[From Bill Powers (2005.01.22.0652 MST)]

Erling Jorgensen (2005.01.21 1310 EST)–

So the question is, is there
something about neural

development that allows certain neurons or ganglia of

neurons to differentiate inbound from outbound? The

prediction of HPCT would be “yes”, if we indeed allow

this feature of comparators to do some of the heavy

lifting, with a meta-monitoring system.

Put that way, I think the answer has to be no. I don’t know of any basis
for distinguishing between inbound and outbound signals. We can’t
conclude that such a basis doesn’t exist, but that doesn’t help
us.
I don’t know how the reorganizing system senses intrinsic variables,
either. Are we talking about something biochemical? Or some special
neural net that permeates the brain (glial cells, which outnumber neurons
10:1 and probably do something?). Maybe if we could answer those
questions we’d see the answer to yours. Basically, I think of the
reorganizing system as an evolved feature of the brain and body. It
evolved to sense those variables that are critical to maintaining life,
whatever they may be. It’s an internalized form of natural selection (as
I think Martin Taylor has said). If comparators are inherited, it’s
possible for there to be inherited connections from their outputs to the
inputs of the reorganizing system, permitting error signals to be
monitored.

I don’t trust that idea much.

In the brain stem, cells in
the olivary nucleus receive

excitatory collaterals from the sensory pathways, and

inhibitory efferent snals from nuclei of the cerebellum

and other sources… the layer is a layer of comparators.

… And of course, the motor cells of the spinal cord are

all comparators.

These are useful anatomical examples from the developed

nervous system. They do not address the inheritabililty

requirement, for how they might have developed.

I assume that the gross neuroanatomical arrangement is
inherited.

So, to specify the prediction a
bit finer: In the developing

nervous system, there would need to be local indicators

(perhaps controlled chemical variables?) such that the

structures that become comparators receive at least one

input each from the collaterals that later are seen to

originate in efferent and afferent pathways, respectively.

If that prediction is borne out by subsequent discoveries,

we should have no problem retaining this aspect of the

model that we are in the process of devising… <:->

I think we can rely on the collaterals and descending tracts being there
as a result of the genetic code plus fairly standardized developmental
processes. The main adjustments resulting from reorganization would be in
the detailed connections that are the last thing to be
established.

Why not just say that the
reorganizing system acts to

reorganize the control system where the error is? The

simple answer is because that’s not enough to account for

all the kinds of learning we see. My stock example is

the bird… [etc.]

The other answer is that the phrase “where is the error is”

is exceedingly ambiguous. Error is a property of loops,

(primarily).

I should have said “where the error signal is.” That’s not
ambiguous.

Now in this discussion, we are
starting to make error a

property of a specific location – i.e., whatever emerges

from an identifiable comparator. But I don’t think we want

reorganization targeted there, because a net change of

sign (inserting an inhibitory interneurone?) might lose

us negative feedback itself.

Good point. The error signal merely indicates roughly where the control
system is. Actually, when we get to this level of detail I realize that
there doesn’t seem to be any place for all the machinery we need. The
glial cells tempt me, but that would be, in our (my) present state of
knowledge of them, about the same as saying that God or Evolution does
it. What we need is a process that will slowly alter synaptic weights in
some hyperspace direction, then begin altering them in a new direction
taken at random, with the speed of the changes depending on the magnitude
of intrinsic error. I know that this way of reorganizing works very well.
All I don’t know is whether or how such a process would be carried out in
a nervous system.

Would the transpose still happen
if the outputs could

only affect a subset of the 500 environmental variables

(say, 200 or 300)? [I’m not sure if that would allow

enough degrees of freedom for stable control to be

established.]

I don’t know. Maybe not. The point of the transpose arrangement is
that it’s as close as you can get to a solution of the 500 simultaneous
equations in 500 variables, which is what you have to have when all the
degrees of freedom have been used up. If there are more degrees of
freedom in the environment than there are control systems, independent
control becomes a lot easier, so maybe the transpose solution isn’t
necessary. Worth trying out.

What I wonder about is the
apparent “experience of errors” part.

With everything else, according to the postulates of PCT,

we only experience “perceptions.” And yet, here, when it
comes

to emotion, I believe there is a more direct experience of

changing errors. This might be an illusion. It might all be

mediated through various kinds of proprioception. Or it

might be the one place where we experience more than our

perceptual inputs.

I have wondered about this, too. I finally decided that what I am calling
“experiences of errors” is really “experiences of the
consequences of error signals.” When you feel fear, you feel (a) the
bodily preparation to flee or fight, and (b) the (conflicting) motor
actions involved in fleeing that result from the error signals in the
hierarchy. I say “conflicting,” but there could also be other
problems that prevent the fleeing from actually taking place.

If so, if this latter intuition
is possible, what might be

the evolutionary reason for such an arrangement? Is there

some kind of functional advantage, that would not mess up

a hierarchy functioning well in other respects?

I don’t like this kind of functional argument. Once you know that some
arrangement exists, you can always think up a reason that it would confer
evolutionary advantages. But if you know the same arrangement is ruled
out, you can think up reasons why it would be disadvantageous. I don’t
think you often see this functional approach used to predict
evolutionary advantage. It shows up mostly in after-the-fact
explanations.

···

=============================

Laundry and shopping are on the list today. Got to go. Appreciate the
comments.

Best,

Bill P.

Re: Conflict and
Reorganization
[Martin Taylor 2005.01.22.11.04]

(How long does it take before I stop writing 2004 space backspace
backspace 5?)

[From Bill Powers (2005.01.22.0652
MST)]

I don’t know how the reorganizing system senses intrinsic variables,
either. Are we talking about something biochemical? Or some special
neural net that permeates the brain (glial cells, which outnumber
neurons 10:1 and probably do something?). Maybe if we could
answer those questions we’d see the answer to yours.

Here’s a pure speculation, but I think it has some of the right
characteristics.

I asked a few times about the effect of broadcast signals, in
other words, signals not targetted to specific recipients (even to
millions of specific recipients). Examples include variations in blood
chemical composition, whether it be simple (CO2, for example) or
complex (e.g. hormones).

One role for some kind of (presumably complex) broadcast signal
might be to alter the likelihood of changing neural connection –
enhancing synaptic growth or the growth or decay of dendrites, …
Such a broacast signal might easily be the result of important
imbalances in intrinsic (chemical) circuits/variables.

That kind of influence of the intrinsic systems on the perceptual
control systems would be unlikely to target particular parts of the
perceptual control hierarchy. But it wouldn’t be impossible, given the
great specificity and complexity involved in systems like the immune
system, not to mention the systems concerned with localized gene
expression. It’s harder, though, for me to see how such chemical
broadcast signals could be derived directly as a function of the
magnitude or dynamics of error signals in the perceptual control
structure, as such.

Knowing almost nothing about the relevant biochemistry, I feel
quite free to make such speculations!

Martin