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luciano@ifqsc.sc.usp.br
Copyright (c) Luciano da Fontoura Costa 1994
Received: August 19, 1994; Accepted: November 2, 1994
PSYCHE, 1(15), January 1995
http://psyche.cs.monash.edu.au/v1/psyche-1-15-dacosta.html
Keywords: cognition, consciousness, computational models of cognition, motivation, retinoids.
Review of: Arnold Trehub (1991) The Cognitive Brain. Cambridge, Mass.: MIT Press. 342 pp. Price: $27.50 pbk. ISBN 0-262-20085-6.
"The next generation of computers will be so intelligent that we will be lucky if they keep us around the house as household pets." (attributed to M. Minsky in Searle (1989)).
1.2 It comes as a surprise to find that a book dealing so comprehensively with cognition fails to address explicitly the mind-brain problem or the philosophical problem of consciousness generally -- in fact, the term 'consciousness' does not even appear in the index, and the term 'mind' appears with but one reference. However, we can find a few passages treating such issues, such as one at the very end of the book: "It is the total specific content, the current physical state of specialized mechanisms in an individual brain shaped by encounters in a world both real and imagined, that constitutes the mind" (p. 305). Such a statement, together with the underlying philosophy adopted throughout the book, suggests that Trehub may be a constructive naturalist (see Flanagan, 1992), one who particularly believes that "we now have sufficient knowledge of the physiology of nerve cells and the structure of the brain to advance the theoretical formulation of putative brain mechanisms that can account for the basic competence of human cognition" (p. 2).
1.3 I begin by briefly looking at some of the principal developments in Trehub's book and follow by continuing from where Trehub leaves off -- i.e., by discussing the implications of Trehub's discussion for consciousness research.
2.2 Accordingly, one of the first steps pursued in the book consists in specifying the assumed basic biophysical properties of neurons, especially the mechanisms through which long- and short-term learning and memory can be achieved, which in turn constrain the universe of possible cognitive models. The dynamics of the long-term mechanisms are assumed to be controlled by the density of the axon transfer factor (ATF) and dendrite transfer factor (DTF), which leads to the reinforcement of those synaptic contacts presenting a reasonable degree of coactivation between pre- and post-synaptic activity (a kind of Hebbian learning). Short-term storage is assumed to be implemented through autaptic cells, a special type of neuron that incorporates synaptical positive feedback through recurrent collaterals of its own axons.
2.3 Those are the basic elements which constitute Trehub's two principal types of neural structures: the synaptic matrix and the retinoid. The former (overall structure given in Figure 1) includes two sub-matrices, namely the imaging matrix and the detection matrix, which are interconnected. The adaptive synapses are capable of long-term learning provided by the dynamic interaction between ATF and DTF. Synaptic matrices receive input at the imaging matrix and produces output from the detection matrix through filter (f) and class (O) cells. Filter cells implement the integration of the input signals relayed by the imaging matrix via the mosaic cells; class cells receive inhibitory input feedback from their own outputs via the reset cell, which is needed in order to implement a kind of `winner-takes-all' mechanism ensuring that only one class cell will activate for each specific input pattern, thus implying that specific stimuli be coded in terms of the relative spike frequency of the class cells. The output lines are feedback into the imaging matrix as a means of implementing associative recall. The synaptic matrix supports not only the ability to learn and recall static semantic representations (associative memory) but also to learn episodic representations, i.e. sequences of symbols temporally correlated (both in vision and in audition). More elaborate cognitive processing can be achieved by interconnecting synaptic matrices.
imaging matrix mosaic detection matrix
cells
input 1 ---->-----.----.----.----.------>------.----.----.----.---
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input 2 ---->-----.----.----.----.------>------.----.----.----.---
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input 3 ---->-----.----.----.----.------>------.----.----.----.---
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input 4 ---->-----.----.----.----.------>------.----.----.----.---
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| | | | V V V V f
| | | | ------/----/----/----/
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| | | | reset ^ V V V V O
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| | | | ------|----|----|----|
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| | | --------------| | | |
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| | ------------------------| | |
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| ----------------------------------| |
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--------------------------------------------|
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out1 out2 out3 out4
Figure 1: General structure of a synaptic matrix.
"V, ^, >" = neurons; "." = adaptive synapse and "/" = inhibitory synapse.2.4 The other basic neural structure in Trehub's approach is the retinoid, a dynamic post-retinal buffer built up of retinotopically organized autaptic neurons providing short-terms storage. Typically, retinoids receive topographical projections from other visual processing and input modules. Retinoids are combined in the retinoid system, which is capable of performing a series of cognitive tasks including: (i) parsing objects; (ii) constructing 3-D representations; (iii) locating and representing the self with respect to a specific environment; (iv) representing paths of movement and; (v) implementing selective attention. An important aspect of the retinoids is that they are organized around the normal foveal axis, which provides a central point for spatial reference. Selective attention, an important perceptual mechanism incorporated into the retinoid system, is achieved via a special reference retinoid, namely the self-locus retinoid, which may "point" to different positions in visual space. Additional mechanisms are incorporated into the system in order to provide stereo visual processing and representations invariant across geometrical transformations -- these latter being invaluable for keeping the number of representations of recognizable elements manageable.
2.5 By using retinoids and synaptic matrices as well as elaborated versions of these structures, Trehub attacks a number of important cognitive processes, including planning, analysis of object relations, composing behaviour, motivation, character recognition, self-directed learning and narrative comprehension. Although a comprehensive discussion of these mechanisms is out of the scope of the present review, some additional remarks are due on specific consciousness-related issues. Identified as the "core function among the executive processes" (p. 295), the cognitive process of motivation is one such. Trehub's analysis of motivation is based upon the hedonic centre, which includes two homeostatic subsystems, designated HS-I (exclusively related to internal processes) and HS-II (related to external, i.e. worldly or "secular" processes). The dynamics of the homeostatic subsystems determine the "pleasure" or "displeasure" of the system; for instance, experimental findings seem to indicate that, upon deviation from the set point (equilibrium) of one of the homeostatic subsystems, suitable actions directed to the restoration of the equilibrium can induce pleasure. The hedonic centre is thus responsible for controlling the individual's actions aimed at the fulfilment of priority goals, which can be achieved through planning (performed by a synaptic matrix system) and action. Another important consciousness-related issue in Trehub's discussion concerns the I-tokens. These are special kinds of autaptic neurons which derive their input from the self-locus retinoid, yielding, when properly interconnected with other active cells, a state of "personal belief." The importance of such special neurons can be immediately appreciated from Trehub's own words: "I-activated predicate tokens, in turn, can evoke sensory images by their chain of backward links to the imaging matrix in a level-1 synaptic matrix. The extended set of such neuronal associations can be taken as the biological substrate for one's sense of self" (p. 302).
3.2 As pointed out by Chalmers (in press), the really tricky issue usually related to consciousness is whether such machines would somehow experience sensations as humans do. Trehub has chosen to avoid such problems altogether, as is clear from his own words: "I must, therefore, acknowledge at the outset that the models I present do not aim to explain directly such ineffable matters as the felt qualities of a breathtaking sunset..." (p. 2). A wise decision, since our current knowledge seems to me too incomplete to support effective scientific work on the issue, although Chalmers (in press) makes a brave attempt in that direction. It should however be emphasized that this does not commit me to dualism or any other sort of mysterianism; my claim, evidently shared by Trehub, is merely that we are not yet in a position to mount an assault on this central philosophical problem of consciousness. No such pessimistic reflections should bother those pragmatic people who, for instance, are interested in understanding many of the neuroscientific aspects of consciousness or who are developing versatile and effective machines that can interact naturally with humans.
Flanagan, O. (1992). Consciousness reconsidered. Cambridge, MA: MIT Press. Book review available
Korb, K. (1991). Searle's AI program. Journal of Experimental and Theoretical AI, 3, 283-296.
Marr, D. (1982). Vision. San Francisco: W. H. Freeman.
Searle, J. (1989). Minds and brains without programs. In C. Blakemore & S. Greenfield (Eds.), Mindwaves. Oxford: Basil Blackwell.
Trehub, A. (1991). The cognitive brain. Cambridge, MA: MIT Press.