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.

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.

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.

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.

QUALITATIVE RESULTS Analysis of the weights produced by training a network is an exceedingly difficult problem, which we have only been able to approach qualitatively. In Figure 1 we present a diagram showing the connection strengths in a network with 651 input units and no hidden units.

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.

ABSTRACT Transient phenomena associated with forward biased silicon p - n - n structures at 4.2K show remarkable similarities with biological neurons. The devices play a role similar to the two-terminal switching elements in Hodgkin-Huxley equivalent circuit diagrams. The devices provide simpler and more realistic neuron emulation than transistors or op-amps. They have such low power and current requirements that they could be used in massive neural networks. Some observed properties of simple circuits containing the devices include action potentials, refractory periods, threshold behavior, excitation, inhibition, summation over synaptic inputs, synaptic weights, temporal integration, memory, network connectivity modification based on experience, pacemaker activity, firing thresholds, coupling to sensors with graded signal outputs and the dependence of firing rate on input current. Transfer functions for simple artificial neurons with spiketrain inputs and spiketrain outputs have been measured and correlated with input coupling.

To illustrate the extent of this additional complexity, Fig. Input 6a shows a schematized circuit for a computational unit of method V

DISCOVERING STRUCfURE FROM MOTION IN MONKEY, MAN AND MACHINE Ralph M. Siegel· The Salk Institute of Biology, La Jolla, Ca. 92037 ABSTRACT The ability to obtain three-dimensional structure from visual motion is important for survival of human and nonhuman primates. Using a parallel processing model, the current work explores how the biological visual system might solve this problem and how the neurophysiologist might go about understanding the solution. In the present work, much effort has been expended mimicking the visual system. This was done for one main reason: the model was designed to help direct physiological experiments in the primate. It was hoped that if an approach for understanding the model could be developed, the approach could then be directed at the primate's visual system.

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.