A generic model of oscillating cortex, which assumes "minimal" coupling justified by known anatomy, is shown to function as an associative memory,using previously developed theory. The network has explicit excitatory neurons with local inhibitory interneuron feedback that forms a set of nonlinear oscillators coupled only by long range excitatofy connections. Using a local Hebb-like learning rule for primary and higher order synapses at the ends of the long range connections, the system learns to store the kinds of oscillation amplitudepatterns observed in olfactory and visual cortex. This rule is derived from a more general "projection algorithm" for recurrent analog networks, that analytically guarantees content addressable memory storage of continuous periodic sequences - capacity: N/2 Fourier components for an N node network - no "spurious" attractors. 1 Introduction This is a sketch of recent results stemming from work which is discussed completely in [1, 2, 3]. Patterns of 40 to 80 hz oscillation have been observed in the large scale activity of olfactory cortex [4] and visual neocortex [5], and shown to predict the olfactory and visual pattern recognition responses of a trained animal.

The brain represents the skin surface as a topographic map in the somatosensory cortex. This map has been shown experimentally to be modifiable in a use-dependent fashion throughout life. We present a neural network simulation of the competitive dynamics underlying this cortical plasticity by detailed analysis of receptive field properties of model neurons during simulations of skin coactivation, corticallesion, digit amputation and nerve section. 1 INTRODUCTION Plasticity of adult somatosensory cortical maps has been demonstrated experimentally in a variety of maps and species (Kass, et al., 1983; Wall, 1988). This report focuses on modelling primary somatosensory cortical plasticity in the adult monkey. We model the long-term consequences of four specific experiments, taken in pairs.

We present two connectionist architectures for chunking of symbolic rewrite rules. One uses backpropagation learning, the other competitive learning. Although they were developed for chunking the same sorts of rules, the two differ in their representational abilities and learning behaviors.

We show that localized activity patterns in a layer of cells, collective excitations, can induce the formation of modular structures in the anatomical connections via a Hebbian learning mechanism. The networks are spatially homogeneous before learning, but the spontaneous emergenceof localized collective excitations and subsequently modularity in the connection patterns breaks translational symmetry. This spontaneous symmetry breaking phenomenon is similar to those which drive pattern formation in reaction-diffusion systems. We have identified requirements on the patterns of lateral connections and on the gains of internal units which are essential for the development of modularity. These essential requirements will most likely remain operative when more complicated (and biologically realistic)models are considered.

In this paper we describe the VLSI design and testing of a high capacity associative memory which we call the exponential correlation 3J.'-CMOSassociative memory (ECAM). The prototype programmable chip is capable of storing 32 memory patterns of 24 bits each. The high capacity of the ECAM is partly due to the use of special exponentiation neurons, which are implemented via MOS transistors in this design. The prototype chipsub-threshold of performing one associative recall in 3 J.'S.is capable 1 ARCHITECTURE Previously (Chiueh, 1989), we have proposed a general model for correlation-based associative memories, which includes a variant of the Hopfield memory and highorder correlation memories as special cases. This new exponential correlation associative (ECAM) possesses a very large storage capacity, which scalesmemory exponentially with the length of memory patterns (Chiueh, 1988).

Most complex behaviors appear to be governed by internal motivational statesor drives that modify an animal's responses to its environment. It is therefore of considerable interest to understand the neural basis of these motivational states. Drawing upon work on the neural basis of feeding in the marine mollusc Aplysia, we have developed a heterogeneous artificial neural network for controlling thefeeding behavior of a simulated insect. We demonstrate that feeding in this artificial insect shares many characteristics with the motivated behavior of natural animals. 1 INTRODUCTION While an animal's external environment certainly plays an extremely important role in shaping its actions, the behavior of even simpler animals is by no means solely reactive. The response of an animal to food, for example, cannot be explained only in terms of the physical stimuli involved. On two different occasions, the very same animal may behave in completely different ways when presented with seemingly identical pieces of food (e.g.

A short account is given of various investigations of neural network properties, beginning with the classic work of McCulloch & Pitts. Early work on neurodynamics and statistical mechanics, analogies with magnetic materials, fault tolerance via parallel distributed processing, memory, learning, and pattern recognition, is described.

Recurrent nets are more powerful than feedforward nets because they allow simulation of dynamical systems. Everything from sine wave generators through computers to the brain are potential candidates, but to use recurrent nets to emulate dynamical systems we need learning algorithms to program them. Here I describe a new twist on an old algorithm for recurrent nets and compare it to its predecessors.

We have done an empirical study of the relation of the number of parameters (weights) in a feedforward net to generalization performance.

This paper explores whether analog circuitry can adequately perform constrainedoptimization. Constrained optimization circuits are designed using the differential multiplier method.