SUMMARY To process sensory data, sensory brain areas must preserve information about both the similarities and differences among learned cues: without the latter, acuity would be lost, whereas without the former, degraded versions of a cue would be erroneously thought to be distinct cues, and would not be recognized. We have constructed a model of piriform cortex incorporating a large number of biophysical, anatomical and physiological parameters, such as two-step excitatory firing thresholds, necessary and sufficient conditions for long-term potentiation (LTP) of synapses, three distinct types of inhibitory currents (short IPSPs, long hyperpolarizing currents (LHP) and long cellspecific afterhyperpolarization (AHP)), sparse connectivity between bulb and layer-II cortex, caudally-flowing excitatory collateral fibers, nonlinear dendritic summation, etc. We have tested the model for its ability to learn similarity-and difference-preserving encodings of incoming sensory cueSj the biological characteristics of the model enable it to produce multiple encodings of each input cue in such a way that different readouts of the cell firing activity of the model preserve both similarity and difference'information. In particular, probabilistic quantal transmitter-release properties of piriform synapses give rise to probabilistic postsynaptic voltage levels which, in combination with the activity of local patches of inhibitory interneurons in layer II, differentially select bursting vs. single-pulsing layer-II cells. Time-locked firing to the theta rhythm (Larson and Lynch, 1986) enables distinct spatial patterns to be read out against a relatively quiescent background firing rate. Training trials using the physiological rules for induction of LTP yield stable layer-II-cell spatial firing patterns for learned cues. Multiple simulated olfactory input patterns (Le., those that share many chemical features) will give rise to strongly-overlapping bulb firing patterns, activating many shared lateral olfactory tract (LOT) axons innervating layer Ia of piriform cortex, which in tum yields highly overlapping layer-II-cell excitatory potentials, enabling this spatial layer-II-cell encoding to preserve the overlap (similarity) among similar inputs. At the same time, those synapses that are enhanced by the learning process cause stronger cell firing, yielding strong, cell-specific afterhyperpolarizing (AHP) currents. Local inhibitory intemeurons effectively select alternate cells to fire once strongly-firing cells have undergone AHP. These alternate cells then activate their caudally-flowing recurrent collaterals, activating distinct populations of synapses in caudal layer lb.

ABSTRACT The potential for presynaptic information processing within the arbor of a single axon will be discussed in this paper. Current knowledge about the activity dependence of the firing threshold, the conditions required for conduction failure, and the similarity of nodes along a single axon will be reviewed. An electronic circuit model for a site of low conduction safety in an axon will be presented. In response to single frequency stimulation the electronic circuit acts as a lowpass filter. I. INTRODUCTION The axon is often modeled as a wire which imposes a fixed delay on a propagating signal.

Patterns of activity over real neural structures are known to exhibit timedependent behavior. It would seem that the brain may be capable of utilizing temporal behavior of activity in neural networks as a way of performing functions which cannot otherwise be easily implemented. These might include the origination of sequential behavior and the recognition of time-dependent stimuli. A model is presented here which uses neuronal populations with recurrent feedback connections in an attempt to observe and describe the resulting time-dependent behavior. Shortcomings and problems inherent to this model are discussed. Current models by other researchers are reviewed and their similarities and differences discussed.

ABSTRACT Intracellular recordings in spinal cord motoneurons and cerebral cortex neurons have provided new evidence on the correlational strength of monosynaptic connections, and the relation between the shapes of postsynaptic potentials and the associated increased firing probability. In these cells, excitatory postsynaptic potentials (EPSPs) produce crosscorrelogram peaks which resemble in large part the derivative of the EPSP. Additional synaptic noise broadens the peak, but the peak area -- i.e., the number of above-chance firings triggered per EPSP -- remains proportional to the EPSP amplitude. The consequences of these data for information processing by polysynaptic connections is discussed. The effects of sequential polysynaptic links can be calculated by convolving the effects of the underlying monosynaptic connections.

DISTRIBUTED NEURAL INFORMATION PROCESSING IN THE VESTIBULO-OCULAR SYSTEM Clifford Lau Office of Naval Research Detach ment Pasadena, CA 91106 Vicente Honrubia* UCLA Division of Head and Neck Surgery Los Angeles, CA 90024 ABSTRACT A new distributed neural information-processing model is proposed to explain the response characteristics of the vestibulo-ocular system and to reflect more accurately the latest anatomical and neurophysiological data on the vestibular afferent fibers and vestibular nuclei. In this model, head motion is sensed topographically by hair cells in the semicircular canals. Hair cell signals are then processed by multiple synapses in the primary afferent neurons which exhibit a continuum of varying dynamics. The model is an application of the concept of "multilayered" neural networks to the description of findings in the bullfrog vestibular nerve, and allows us to formulate mathematically the behavior of an assembly of neurons whose physiological characteristics vary according to their anatomical properties. INTRODUCTION Traditionally the physiological properties of individual vestibular afferent neurons have been modeled as a linear time-invariant system based on Steinhausents description of cupular motion.

ABSTRACT The potential for presynaptic information processing within the arbor of a single axon will be discussed in this paper. Current knowledge about the activity dependence of the firing threshold, the conditions required for conduction failure, and the similarity of nodes along a single axon will be reviewed. An electronic circuit model for a site of low conduction safety in an axon will be presented. In response to single frequency stimulation the electronic circuit acts as a lowpass filter. I. INTRODUCTION The axon is often modeled as a wire which imposes a fixed delay on a propagating signal.

This arises from the parallelism and distributed knowledge representation which gives rise to gentle degradation as faults appear. These functions are attractive to implementation in VLSI and WSI. For example, the natural fault - tolerance could be useful in silicon wafers with imperfect yield, where the network degradation is approximately proportional to the non-functioning silicon area. To cast neural networks in engineering language, a neuron is a state machine that is either "on" or "off', which in general assumes intermediate states as it switches smoothly between these extrema. The synapses weighting the signals from a transmitting neuron such that it is more or less excitatory or inhibitory to the receiving neuron. The set of synaptic weights determines the stable states and represents the learned information in a system. The neural state, VI' is related to the total neural activity stimulated by inputs to the neuron through an activation junction, F. Neural activity is the level of excitation of the neuron and the activation is the way it reacts in a response to a change in activation.

A Computer Simulation of Olfactory Cortex With Functional Implications for Storage and Retrieval of Olfactory Information Matthew A. Wilson and James M. Bower Computation and Neural Systems Program Division of Biology, California Institute of Technology, Pasadena, CA 91125 ABSTRACT Based on anatomical and physiological data, we have developed a computer simulation of piriform (olfactory) cortex which is capable of reproducing spatial and temporal patterns of actual cortical activity under a variety of conditions. Using a simple Hebb-type learning rule in conjunction with the cortical dynamics which emerge from the anatomical and physiological organization of the model, the simulations are capable of establishing cortical representations for different input patterns. The basis of these representations lies in the interaction of sparsely distributed, highly divergent/convergent interconnections between modeled neurons. We have shown that different representations can be stored with minimal interference. Further, we have demonstrated that the degree of overlap of cortical representations for different stimuli can also be modulated. Both features are presumably important in classifying olfactory stimuli.

ABSTRACT A single cell theory for the development of selectivity and ocular dominance in visual cortex has been presented previously by Bienenstock, Cooper and Munrol. This has been extended to a network applicable to layer IV of visual cortex 2. In this paper we present a mean field approximation that captures in a fairly transparent manner the qualitative, and many of the quantitative, results of the network theory. Finally, we consider the application of this theory to artificial neural networks and show that a significant reduction in architectural complexity is possible. A SINGLE LAYER NETWORK AND THE MEAN FIELD APPROXIMATION We consider a single layer network of ideal neurons which receive signals from outside of the layer and from cells within the layer (Figure 1). The activity of the ith cell in the network is c' - m' d J d is a vector of afferent signals to the network. Each cell receives input from n fibers outside of the cortical network through the matrix of synapses mi' Intra-layer input to each cell is then transmitted through the matrix of cortico-cortical synapses L. Light circles are the LGN -cortical synapses.

ABSTRACT A single cell theory for the development of selectivity and ocular dominance in visual cortex has been presented previously by Bienenstock, Cooper and Munrol. This has been extended to a network applicable to layer IV of visual cortex 2. In this paper we present a mean field approximation that captures in a fairly transparent manner the qualitative, and many of the quantitative, results of the network theory. Finally, we consider the application of this theory to artificial neural networks and show that a significant reduction in architectural complexity is possible. A SINGLE LAYER NETWORK AND THE MEAN FIELD APPROXIMATION We consider a single layer network of ideal neurons which receive signals from outside of the layer and from cells within the layer (Figure 1). The activity of the ith cell in the network is c' - m' d J d is a vector of afferent signals to the network. Each cell receives input from n fibers outside of the cortical network through the matrix of synapses mi' Intra-layer input to each cell is then transmitted through the matrix of cortico-cortical synapses L. Light circles are the LGN -cortical synapses.