Centric Models of the Orientation Map in Primary Visual Cortex William Baxter Department of Computer Science, S.U.N.Y. at Buffalo, NY 14620 Bruce Dow Department of Physiology, S.U.N.Y. at Buffalo, NY 14620 Abstract In the visual cortex of the monkey the horizontal organization of the preferred orientations of orientation-selective cells follows two opposing rules: 1) neighbors tend to have similar orientation preferences, and 2) many different orientations are observed in a local region. Several orientation models which satisfy these constraints are found to differ in the spacing and the topological index of their singularities. Using the rate of orientation change as a measure, the models are compared to published experimental results. Introduction It has been known for some years that there exist orientation-sensitive neurons in the visual cortex of cats and mOnkeysl,2. These cells react to highly specific patterns of light occurring in narrowly circumscribed regiOns of the visual field, i.e., the cell's receptive field. The best patterns for such cells are typically not diffuse levels of illumination, but elongated bars or edges oriented at specific angles.

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.

Recently, many modifications to the McCulloch/Pitts model have been proposed where both learning and forgetting occur. Given that the network never saturates (ceases to function effectively due to an overload of information), the learning updates can continue indefinitely. For these networks, we need to introduce performance measmes in addition to the information capacity to evaluate the different networks. We mathematically define quantities such as the plasticity of a network, the efficacy of an information vector, and the probability of network saturation. From these quantities we analytically compare different networks.

How Neural Nets Work Alan Lapedes Robert Farber Theoretical Division Los Alamos National Laboratory Los Alamos, NM 87545 Abstract: There is presently great interest in the abilities of neural networks to mimic "qualitative reasoning" by manipulating neural incodings of symbols. Less work has been performed on using neural networks to process floating point numbers and it is sometimes stated that neural networks are somehow inherently inaccurate and therefore best suited for "fuzzy" qualitative reasoning. Nevertheless, the potential speed of massively parallel operations make neural net "number crunching" an interesting topic to explore. In this paper we discuss some of our work in which we demonstrate that for certain applications neural networks can achieve significantly higher numerical accuracy than more conventional techniques. In particular, prediction of future values of a chaotic time series can be performed with exceptionally high accuracy. We analyze how a neural net is able to do this, and in the process show that a large class of functions from Rn. Rffl may be accurately approximated by a backpropagation neural net with just two "hidden" layers. The network uses this functional approximation to perform either interpolation (signal processing applications) or extrapolation (symbol processing applicationsJ.

REFLEXIVE ASSOCIATIVE MEMORIES Hendrlcus G. Loos Laguna Research Laboratory, Fallbrook, CA 92028-9765 ABSTRACT In the synchronous discrete model, the average memory capacity of bidirectional associative memories (BAMs) is compared with that of Hopfield memories, by means of a calculat10n of the percentage of good recall for 100 random BAMs of dimension 64x64, for different numbers of stored vectors. The memory capac1ty Is found to be much smal1er than the Kosko upper bound, which Is the lesser of the two dimensions of the BAM. On the average, a 64x64 BAM has about 68 % of the capacity of the corresponding Hopfield memory with the same number of neurons. The memory capacity limitations are due to spurious stable states, which arise In BAMs In much the same way as in Hopfleld memories. Occurrence of spurious stable states can be avoided by replacing the thresholding in the backlayer of the BAM by another nonl1near process, here called "Dominant Label Selection" (DLS).

W. Scott Stornetta Stanford University, Physics Department, Stanford, Ca., 94305 Tad Hogg and B. A. Huberman Xerox Palo Alto Research Center, Palo Alto, Ca. 94304 ABSTRACT Recognizing patterns with temporal context is important for such tasks as speech recognition, motion detection and signature verification. We propose an architecture in which time serves as its own representation, and temporal context is encoded in the state of the nodes. We contrast this with the approach of replicating portions of the architecture to represent time. As one example of these ideas, we demonstrate an architecture with capacitive inputs serving as temporal feature detectors in an otherwise standard back propagation model. Experiments involving motion detection and word discrimination serve to illustrate novel features of the system.

In biological systems, it relates to such issues as classical and operant conditioning, temporal coordination of sensorimotor systems and temporal reasoning. In artificial systems, it addresses such real-world tasks as robot control, speech recognition, dynamic image processing, moving target detection by sonars or radars, EEG diagnosis, and seismic signal processing.

ABSTRACT How does the connectivity of a neural network (number of synapses per neuron) relate to the complexity of the problems it can handle (measured by the entropy)? Switching theory would suggest no relation at all, since all Boolean functions can be implemented using a circuit with very low connectivity (e.g., using two-input NAND gates). However, for a network that learns a problem from examples using a local learning rule, we prove that the entropy of the problem becomes a lower bound for the connectivity of the network. INTRODUCTION The most distinguishing feature of neural networks is their ability to spontaneously learn the desired function from'training' samples, i.e., their ability to program themselves. Clearly, a given neural network cannot just learn any function, there must be some restrictions on which networks can learn which functions.

ON TROPISTIC PROCESSING AND ITS APPLICATIONS Manuel F. Fernandez General Electric Advanced Technology Laboratories Syracuse, New York 13221 ABSTRACT The interaction of a set of tropisms is sufficient in many cases to explain the seemingly complex behavioral responses exhibited by varied classes of biological systems to combinations of stimuli. It can be shown that a straightforward generalization of the tropism phenomenon allows the efficient implementation of effective algorithms which appear to respond "intelligently" to changing environmental conditions. Examples of the utilization of tropistic processing techniques will be presented in this paper in applications entailing simulated behavior synthesis, path-planning, pattern analysis (clustering), and engineering design optimization. INTRODUCTION The goal of this paper is to present an intuitive overview of a general unsupervised procedure for addressing a variety of system control and cost minimization problems. This procedure is hased on the idea of utilizing "stimuli" produced by the environment in which the systems are designed to operate as basis for dynamically providing the necessary system parameter updates.

Many optimization models of neural networks need constraints to restrict the space of outputs to a subspace which satisfies external criteria. Optimizations using energy methods yield "forces" which act upon the state of the neural network. The penalty method, in which quadratic energy constraints are added to an existing optimization energy, has become popular recently, but is not guaranteed to satisfy the constraint conditions when there are other forces on the neural model or when there are multiple constraints. In this paper, we present the basic differential multiplier method (BDMM), which satisfies constraints exactly; we create forces which gradually apply the constraints over time, using "neurons" that estimate Lagrange multipliers. The basic differential multiplier method is a differential version of the method of multipliers from Numerical Analysis.