This paper describes an approach to integrated segmentation and recognition of hand-printed characters. The approach, called Saccade, integrates ballistic and corrective saccades (eye movements) with character recognition. A single backpropagation net is trained to make a classification decision on a character centered in its input window, as well as to estimate the distance of the current and next character from the center of the input window. The net learns to accurately estimate these distances regardless of variations in character width, spacing between characters, writing style and other factors.

We describe a model of visual word recognition that accounts for several aspects of the temporal processing of sequences of briefly presented words. The model utilizes a new representation for written words, based on dynamic time warping and multidimensional scaling. The visual input passes through cascaded perceptual, comparison, and detection stages. We describe how these dynamical processes can account for several aspects of word recognition, including repetition priming and repetition blindness.

It is known from biological data that the response patterns of interneurons in the olfactory macroglomerulus (MGC) of insects are of central importance for the coding of the olfactory signal. We propose an analytically tractable model of the MGC which allows us to relate the distribution of response patterns to the architecture of the network.

Electrophysiological studies (Cynader and Berman 1972, Robinson 1972) showed that the intermediate layer of SC is topographically organized into a motor map. The location of active neurons in this area was found to be related to the oculomotor error (Le.

This paper examines and extends the work of Linsker (1986) on self organising feature detectors. Linsker concentrates on the visual processing system, but infers that the weak assumptions made will allow the model to be used in the processing of other sensory information. This claim is examined here, with special attention paid to the auditory system, where there is much lower connectivity and therefore more statistical variability. Online training is utilised, to obtain an idea of training times. These are then compared to the time available to prenatal mammals for the formation of feature sensitive cells. 1 INTRODUCTION Within the last thirty years, a great deal of research has been carried out in an attempt to understand the development of cells in the pathways between the sensory apparatus and the cortex in mammals. For example, theories for the development of feature detectors were forwarded by Nass and Cooper (1975), by Grossberg (1976) and more recently Obermayer et al (1990). Hubel and Wiesel (1961) established the existence of several different types of feature sensitive cell in the visual cortex of cats. Various subsequent experiments have 1007 1008 Walton and Bisset shown that a considerable amount of development takes place before birth (i.e.

The formation of propagating spiral waves is studied in a randomly connected neural network composed of integrate-and-fire neurons with recovery period and excitatory connections using computer simulations. Network activity is initiated by periodic stimulation at a single point. The results suggest that spiral waves can arise in such a network via a sub-critical Hopf bifurcation. 1 Introduction

This is motivated by experimental evidence that these phenomena may be subserved by the same mechanisms. An important aspect of this model is that ocular dominance segregation can occur when input activity is both distributed, and positively correlated between the eyes. This allows investigation of the dependence of the pattern of ocular dominance stripes on the degree of correlation between the eyes: it is found that increasing correlation leads to narrower stripes. Experiments are suggested to test whether such behaviour occurs in the natural system.

A switching between apparently coherent (oscillatory) and stochastic episodes of activity has been observed in responses from cat and monkey visual cortex. We describe the dynamics of these phenomena in two parallel approaches, a phenomenological and a rather microscopic one. On the one hand we analyze neuronal responses in terms of a hidden state model (HSM). The parameters of this model are extracted directly from experimental spike trains. They characterize the underlying dynamics as well as the coupling of individual neurons to the network. This phenomenological model thus provides a new framework for the experimental analysis of network dynamics.

We present a local learning rule in which Hebbian learning is conditional on an incorrect prediction of a reinforcement signal. We propose a biological interpretation of such a framework and display its utility through examples in which the reinforcement signal is cast as the delivery of a neuromodulator to its target. Three exam pIes are presented which illustrate how this framework can be applied to the development of the oculomotor system. 1 INTRODUCTION Activity-dependent accounts of the self-organization of the vertebrate brain have relied ubiquitously on correlational (mainly Hebbian) rules to drive synaptic learning. In the brain, a major problem for any such unsupervised rule is that many different kinds of correlations exist at approximately the same time scales and each is effectively noise to the next. For example, relationships within and between the retinae among variables such as color, motion, and topography may mask one another and disrupt their appropriate segregation at the level of the thalamus or cortex.

The vestibulo-ocular reflex (VOR) is a compensatory eye movement that stabilizes images on the retina during head turns. Its magnitude, or gain, can be modified by visual experience during head movements. Possible learning mechanisms for this adaptation have been explored in a model of the oculomotor system based on anatomical and physiological constraints. The local correlational learning rules in our model reproduce the adaptation and behavior of the VOR under certain parameter conditions. From these conditions, predictions for the time course of adaptation at the learning sites are made. 1 INTRODUCTION The primate oculomotor system is capable of maintaining the image of an object on the fovea even when the head and object are moving simultaneously.