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sensory input which is used, in the first place, to construct our world lor <r...l
model and, also, serves the function of continually monitoring and/or
Perceptual Error
adjusting this model to achieve a close correspondence between the model and Signal, p S1gnol,8
the world.
The most basic type of cybernetic model was proposed by Wiener (194B)
in the form of a single loop control system that contained five variables Input Oulput
FUllction System Func I/on
(Figure 1).
fijl~'K~
SYS1U1'S
XL + e K
Physlcol
SlImull Proximal Resulls
Physlcol
Laws Physical
Laws
X 0, ~ 1
OIlflUllli lI1HlllY na
32 33
systems we can, in general, distinguish three types of reference signals, system is in general too simplistic. Rather we deal with a hierarchy of
arranged hierarchically: horizontally as well as vertically interconnecting subcontrol systems where
a) Genetic:generated by DNA, RNA the e signals from one such subcontrol system become the p or r signals of
b) Intrinsic:generated by neuro-chemical reactions e.g., hormones other subsystems. Secondly, the most efficient type of control systems are
c) Acquired:generated by experience those which have a model of the controlled quantity K as part of their
All three types generate r values which are appropriate for specific system, an arrangement that leads to the optimal performance of such systems.
objectives at a given time and for a given state of the organism. The Figure 3 is an example of such a system.
genetic r signals must be regarded as more or less fixed, i.e., only subject Another important feature of incorporating a model of K into the system
to alteration under highly unusual (abnormal) conditions (e.g., X-ray is that the model can take on different parameters as a function of other
radiation), the intrinsic r signals are flexible within certain limits, and control systems, i.e., it can be a flexible component. Most control systems
acquired r-values have the greatest flexibility. From the perspective of operate on the principle of negative feedback where the objective is to
REST effects, the intrinsic and acquired r signal s have the greatest stabil ize the system at a given, constant value. Indeed, these types of
flexibility since the efforts of the organism in response to reduced levels systems are inherently unable to deal with positive feedback, i.e., where
of stimulation can readily be regarded as attempts to reinstate the equation the e signal produces (via K) greater and greater values of the p signal.
p = r by some means. Some types of control loops, however, are susceptible to positive feedback
in that this type of feedback leads to adjustments in the control loop and
here one can point to the model within the system as that component which
will respond to the positive feedback by altering its parameters.
The above considerations are drawn from systems engineering, and while
®~~®
c;cnU'AHAllHt similar or analogous control loops do exist in organisms with nervous
I' systems, an interesting case of the present discussion arises where the
.
(",lth aodcl of 10K")
model is not only a model of the controll ed quant ity, but al so a second
comparator that monitors, integrates and regulates some other important
I functions of the system itself. One specific example that would fall into
COtll'ARAl'oR this category is the regulation of sensory thresholds by an organism exposed
to sensory restriction. By assigning to the concept of "optimal level of
-~- ...__ .-_ .. ~ .... ------_..._....-_.._...- ..._.-_._... \timulation" a reference signal "ro " set at a certain value, the following
relationships can be diagramed:
K
The following interactions arise out of the relationships given
in Figure 4.
a) Sensory signals (P) go to both cortical and subcortical regions
in this case the reticular formation.
F I~,"~e 3. A Control system wJtt, an JIIlorllal
model of the controlled qu.'llilil Y K. b) The controlled quantity (K,) is the amount of afferent neural
excitation that is passed on to higher order neurons from lower
order neurons. Normally this amount is held below maximum
Before going into a specific example, two additional points must I", channel capacity by tonic inhibition (sensory gating) exerted by
considered. For one, the view of the organism as a single cybernetic contrlll efferent neural signals.
34 35
OrTlflAl. I.EVEI. or STlIlUl.ATIOff Assuming linear approximations, one can derive the foll owi ng set of
equations:
1. e = r - p
r (0)
2. p = Ke
3. p = K(r - p)
" (e)
4. p = KL
I + K
(ANAS)
For systems with more than one controlled quantity, equation (4) expands to
incorporate the different values of K.
"(NI)
In the case of 2 k variables of interest, equation (4) can be written
(in simplified form) as:
5, p = t'.,_r_
• (I)
_ _ _ _ •• _ .. _1 • , _••• _•• _ __ _. ._ . I + K2
If K2 represents a given unit of time, the value of p will represent the
k SUISOKY' Itf.S1M leTIUN loop gain of the system per unit time, and equation (5) will generate a
1
negatively accelerated curve that after a given time stabilizes at an
,,'jlju["e 4. A cybernetic JQodel of 8el~ory (jatinq. asymptotic level.
Now, this function fits quite well with empirical findings on the
I'rFect of sensory restriction on changes in sensory sensitivity. Taking some
c) The amount of afferent signals not subject to tonic inhibition d.lta from Bross and Zubek (1975) on the effect of 14 days of auditory
is regulated by the arousal states (needs) of relevant cortical r'('striction (silence) on the critical flicker frequency (CFF) of the eye and
processes (r o ) ' Il'lting K2 being equal to days of auditory restriction, K, set at optimum
d) Any inequality of p~ or r~ leads to a change in the reference PlFiciency for transduction (i.e., a value of 1.0), and r as an ad hoc
signal r AF for the reticular formation which results in: "pproximation of 2.0, the fit between the observed and predicted function is
I) a change in the value of the error signal e w normally (in ',hown in Figure 5.
the case of sensory restriction) a negative value which in In principle, one can move from specific subsystems which comprise the
turn would lower the amount of tonic inhibition in the lllllltitude of functions a living organism carries out to a perspective whir·
sensory gate, and, n''1ards the organism as a single cybernetic system by focussing on
2) a change in the val ue of e la" whose pathways can be regarded ,orllTol functions the organism carries out. For example. a ma,i"
as belonging to the ARAS, will lead to an increase in loop must be the organism's attempt to generate and maintain
arousal signal s to cortical areas to compensate for the 0' the world where the collective perceptual signals are r
input usually received via classical sensory pathways (p), 10 Ipst the correctness or val idity of that model, P
These relationships can be stated in a formal manner and cast in mathematical II,,· introduction, given the way we process in f
«'
36
orrltlAl. I.EVE•. OF STltlUl.ATION Assuming linear approximations, one can derive the following set of
equations:
1. e = r - p
r (0)
2. p Ke
=
3. p = K(r - p)
0' (e)
4. p = KL
1+ K
(ARAS)
For systems with more than one controlled quantity, equation (4) expands to
incorporate the different values of K.
I'(H)
In the case of 2 k variables of interest, equation (4) can be written
(in simplified form) as:
5. P = ]c;,_r_
• •..•. 1-,..-,-----1.••• •••••• •. .•..- . - - - - -.•.••...••••••.••••••• 1 + K,
If K, represents a given unit of time, the val ue of p will represent the
t:: StJISOMY Mt:SIMlt..:TlUN
loop gain of the system per unit time, and equation (5) will generate a
2
negatively accelerated curve that after a given time stabil izes at an
t"hJure 4. 1\ cylJernetJc Klodel of sCllJ50ry qat.inq.
asymptotic level.
Now, this function fits quite well with empirical findings on the
effect of sensory restriction on changes in sensory sensitivity. Taking some
c) The amount of afferent signals not subject to tonic inhibition data from Bross and Zubek (1975) on the effect of 14 days of auditory
is regulated by the arousal states (needs) of relevant cortical restriction (silence) on the critical flicker frequency (CFF) of the eye and
letting K, being equal to days of auditory restriction, K, set at optimum
processes (r o ) '
d) Any inequality of p~ or r M leads to a change in the reference efficiency for transduction (i.e., a value of 1.0), and r as an ad hoc
signal r~ for the reticular formation which results in: approximation of 2.0, the fit between the observed and predicted function is
1) a change in the value of the error signal e w normally (in shown in Figure 5.
the case of sensory restriction) a negative value which in In principle, one can move from specific subsystems which comprise the
turn would lower the amount of tonic inhibition in the owltitude of functions a living organism carries out to a perspective which
f(>gards the organism as a single cybernetic system by focussing on major
sensory gate, and,
I llntrol functions the organism carries out. For example, a major control
2) a change in the value of e la" whose pathways can be regarded
as belonging to the ARAS, will lead to an increase in IllllP must be the organism's attempt to generate and maintain a stable model
III the world where the collective perceptual signals are constantly utilized
arousal signals to cortical areas to compensate for the
input usually received via classical sensory pathways (p). I II test the correctness or val idity of that model. As briefly alluded to in
Ihp introduction, given the way we process information about the world a
These relationships can be stated in a formal manner and cast in mathematical
'.1 r'llng case can be made that we experience the world in this inductive
form.
OJ.lllller. For thi s case a cybernet i c approach to REST effects can make some
11I11'r'psting, testable predictions. Given that the role of sensory/perceptual
'.1I11,aI5 is critical to the maintenance of such a model, the controlled
36
37
44.5, 5
I
~
¥ of the variables involved such as length of SR, type of SR and so on, but it
could easily be applied to specific situations.
44.0 .
~ A second instance where an interesting and also unique prediction can
o
be generated from the cybernetic model of REST is in the area of adaptation
z
a
N"l.S 3 to novel perceptual environments. Given that sensory reduction entails a
p significant decrease in the individual's ability to monitor the validity or
'"'
W
0..
2
~ "3.01_ ", '
correctness of his/her world model via sensory feedback, it should follow
'I~
3il
39
1ikely to represent "software" rather than "hardware" control systems, a Suedfeld, P. Restricted Environmental Stimulation: Research and Clinical
feature that makes them readily amendable to alterations and adjustments. Applications. New York, NY: John Wiley and Sons, 1980.
The considerable evidence on the facil itatory effect of REST on attitude Vernon, J. Inside the Black Room. New York, NY: Clarkson, 1963.
change, changes in self image etc., can be drawn upon in support of this Welch, R.B. Perceptual Modification: Adapting to Altered Sensory
contention. Environments. New York, NY: Academic Press, 1978.
The arguments presented in this paper do not, of course, present an Wiener, N. Cybernetics. New York, NY: Wiley & Sons, 1948.
exhaustive analysis of the viability of cybernetic theory to REST. The Zubek, J. P. (Ed.) Sensory Depri vat i on: Fi fteen Years of Research. New
specific implications of such an approach will have to be worked out in much York, NY: Appleton-Century-Crofts, 1969.
greater detail and subjected to empirical tests. The promise this approach Zuckerman, M. Theoretical formulations: 1. In: Zubek, J.P. (Ed.) Sensory
holds, in addition to presenting a more unified view of REST phenomena, is Deprivation: Fifteen Years of Research. New York, NY: Appleton
that it will lead to a perspective that will enable investigators to identify Century-Crofts, 1969.
the reference signals, levels of control, and the controlled quantities by
which we maintain our everyday behavior and expectations about the world, as
well as our attempts to change these behaviors and expectations.
REFERENCES
Bross, M. & Zubek, J.P. Progressive increase in the CFF of the non-occluded
eye during prolonged monocul ar deprivation. Canadian Journal of
Psychology, 1972, 29, 340-347.
Budzynski, T.H. Biofeedback and the twilight states of consciousness. In:
Schwartz, G.E. & Shapiro, D. (Eds.) Consciousness and Self-Regulation:
Advances in Research, IV New York, NY: Plenum, 1976.
Held, R. & Hein, A. Adaptation of disarranged hand-eye coordination
contingent upon reafferent stimulation. Perceptual and Motor Skills,
1958, .6., 87-90.
Hutchison, M. The Book of Floating. New York, NY: Morrow &Co., Inc., 1984.
Kohler, 1. The formation and transformation of the perceptual world.
Psychological Issues, 1964, 1.
MacLean, P.O. The triune brain, emotion, and scientific bias. In: Schmitt.
F.O. (Ed.) The Neurosciences. New York, NY: Rockefeller University.
1970, 336-348.
Powers, W.T. Behavior: The Control of Perception. Chicago, IL: Aldint',
1973,
Schultz, D.P. Sensory Restriction. New York, NY: Academic Press, 1965.
Suedfeld, P. Theoretical formulations: II. In: Zubek, J.P. (Ed.) Sensory
Deprivation: Fifteen Years of Research. New York, NY: Applel.oll
Century-Crofts, 1969, 433-448.
40 41