The parietal cortex is thought to represent the egocentric positions of objects in particular coordinate systems. We propose an alternative approach to spatial perception of objects in the parietal cortex from the perspective of sensorimotor transformations. The responses of single parietal neurons can be modeled as a gaussian function of retinal position multiplied by a sigmoid function of eye position, which form a set of basis functions. We show here how these basis functions can be used to generate receptive fields in either retinotopic or head-centered coordinates by simple linear transformations. This raises the possibility that the parietal cortex does not attempt to compute the positions of objects in a particular frame of reference but instead computes a general purpose representation of the retinal location and eye position from which any transformation can be synthesized by direct projection. This representation predicts that hemineglect, a neurological syndrome produced by parietal lesions, should not be confined to egocentric coordinates, but should be observed in multiple frames of reference in single patients, a prediction supported by several experiments.

We implement and study a computational model of Stevens' [19921 theory of the pathogenesis of schizophrenia. This theory hypothesizes that the onset of schizophrenia is associated with reactive synaptic regeneration occurring in brain regions receiving degenerating temporal lobe projections. Concentrating on one such area, the frontal cortex, we model a frontal module as an associative memory neural network whose input synapses represent incoming temporal projections. We analyze how, in the face of weakened external input projections, compensatory strengthening of internal synaptic connections and increased noise levels can maintain memory capacities (which are generally preserved in schizophrenia). However, These compensatory changes adversely lead to spontaneous, biased retrieval of stored memories, which corresponds to the occurrence of schizophrenic delusions and hallucinations without any apparent external trigger, and for their tendency to concentrate on just few central themes. Our results explain why these symptoms tend to wane as schizophrenia progresses, and why delayed therapeutical intervention leads to a much slower response.

Accumulating data from neurophysiology and neuropsychology have suggested two information processing roles for prefrontal cortex (PFC): 1) short-term active memory; and 2) inhibition. We present a new behavioral task and a computational model which were developed in parallel. The task was developed to probe both of these prefrontal functions simultaneously, and produces a rich set of behavioral data that act as constraints on the model. The model is implemented in continuous-time, thus providing a natural framework in which to study the temporal dynamics of processing in the task. We show how the model can be used to examine the behavioral consequences of neuromodulation in PFC. Specifically, we use the model to make novel and testable predictions regarding the behavioral performance of schizophrenics, who are hypothesized to suffer from reduced dopaminergic tone in this brain area.

In young barn owls raised with optical prisms over their eyes, these auditory maps are shifted to stay in register with the visual map, suggesting that the visual input imposes a frame of reference on the auditory maps. However, the optic tectum, the first site of convergence of visual with auditory information, is not the site of plasticity for the shift of the auditory maps; the plasticity occurs instead in the inferior colliculus, which contains an auditory map and projects into the optic tectum. We explored a model of the owl remapping in which a global reinforcement signal whose delivery is controlled by visual foveation. A hebb learning rule gated by reinforcement learned to appropriately adjust auditory maps. In addition, reinforcement learning preferentially adjusted the weights in the inferior colliculus, as in the owl brain, even though the weights were allowed to change throughout the auditory system. This observation raises the possibility that the site of learning does not have to be genetically specified, but could be determined by how the learning procedure interacts with the network architecture.

The macaque lateral geniculate nucleus (LGN) exhibits an intricate lamination pattern, which changes midway through the nucleus at a point coincident with small gaps due to the blind spot in the retina. We present a three-dimensional model of morphogenesis in which local cell interactions cause a wave of development of neuronal receptive fields to propagate through the nucleus and establish two distinct lamination patterns. We examine the interactions between the wave and the localized singularities due to the gaps, and find that the gaps induce the change in lamination pattern. We explore critical factors which determine general LGN organization.

Our results show that maximal diversity of neuronal response properties is attained when the ratio of dendritic and axonal arbor sizes is equal to 1, a value found in many cortical areas and across species (Lund et al., 1993; Malach, 1994). Maximization of diversity also leads to better performance in systems of receptive fields implementing steerablejshiftable filters, which may be necessary for generating the seemingly continuous range of orientation selectivity found in VI, and in ma.tching spatially distributed signals. This cortical organization principle may, therefore, have the double advantage of accounting for the formation of the cortical columns and the associated patchy projection patterns, and of explaining how systems of receptive fields can support functions such as the generation of precise response tuning from imprecise distributed inputs, and the matching of distributed signals, a problem that arises in visual tasks such as stereopsis, motion processing, and recognition.

For example, in the normal visual cortex, long-range lateral connections link areas with similar orientation preference (Gilbert and Wiesel 1989). Like cortical response properties, the connectivity pattern is highly plastic in early development and can be altered by experience (Katz and Callaway 1992). In a cat that is brought up squint-eyed from birth, the lateral connections link areas with the same ocular dominance instead of orientation (Lowel and Singer 1992). Such patterned lateral connections develop at the same time as the orientation selectivity and ocular dominance itself (Burkhalter et al.1993;

Songbirds learn to imitate a tutor song through auditory and motor learning. We have developed a theoretical framework for song learning that accounts for response properties of neurons that have been observed in many of the nuclei that are involved in song learning. Specifically, we suggest that the anteriorforebrain pathway, which is not needed for song production in the adult but is essential for song acquisition, provides synaptic perturbations and adaptive evaluations for syllable vocalization learning. A computer model based on reinforcement learning was constructed that could replicate a real zebra finch song with 90% accuracy based on a spectrographic measure. The second generation of the birdsong model replicated the tutor song with 96% accuracy.

More than ten of the most prominent models for the structure and for the activity dependent formation of orientation and ocular dominance columns in the striate cort( x have been evaluated. We implemented those models on parallel machines, we extensively explored parameter space, and we quantitatively compared model predictions with experimental data which were recorded optically from macaque striate cortex. In our contribution we present a summary of our results to date. Briefly, we find that (i) despite apparent differences, many models are based on similar principles and, consequently, make similar predictions, (ii) certain "pattern models" as well as the developmental "correlation-based learning" models disagree with the experimental data, and (iii) of the models we have investigated, "competitive Hebbian" models and the recent model of Swindale provide the best match with experimental data. 1 Models and Data The models for the formation and structure of orientation and ocular dominance columns which we have investigated are summarized in table 1. Models fall into two categories: "Pattern models" whose aim is to achieve a concise description of the observed patterns and "developmental models" which are focussed on the pro- 94

A biological neuron can be viewed as a device that maps a multidimensional temporal event signal (dendritic postsynaptic activations) into a unidimensional temporal event signal (action potentials). We have designed a network, the Spatio-Temporal Event Mapping (STEM) architecture, which can learn to perform this mapping for arbitrary biophysical models of neurons. Such a network appropriately trained, called a STEM cell, can be used in place of a conventional compartmental model in simulations where only the transfer function is important, such as network simulations. The STEM cell offers advantages over compartmental models in terms of computational efficiency, analytical tractabili1ty, and as a framework for VLSI implementations of biological neurons.