Abstract Missing

We investigate the computational power of a formal model for networks of spiking neurons, both for the assumption of an unlimited timing precision, and for the case of a limited timing precision. We also prove upper and lower bounds for the number of examples that are needed to train such networks.

In the last decade the outlines of the neural structures subserving the sense of direction have begun to emerge. Several investigations have shed light on the effects of vestibular input and visual input on the head direction representation. In this paper, a model is formulated of the neural mechanisms underlying the head direction system. The model is built out of simple ingredients, depending on nothing more complicated than connectional specificity, attractor dynamics, Hebbian learning, and sigmoidal nonlinearities, but it behaves in a sophisticated way and is consistent with most of the observed properties ofreal head direction cells. In addition it makes a number of predictions that ought to be testable by reasonably straightforward experiments.

Previous investigators have suggested that these cells may represent self-motion. Spiral patterns can also be generated by the relative motion of the observer and a particular object. An MST cell may then account for some portion of the complex flow field, and the set of active cells could encode the entire flow; in this manner, MST effectively segments moving objects. Such a grouping operation is essential in interpreting scenes containing several independent moving objects and observer motion. We describe a model based on the hypothesis that the selective tuning of MST cells reflects the grouping of object components undergoing coherent motion. Inputs to the model were generated from sequences of ray-traced images that simulated realistic motion situations, combining observer motion, eye movements, and independent object motion. The input representation was modeled after response properties of neurons in area MT, which provides the primary input to area MST. After applying an unsupervised learning algorithm, the units became tuned to patterns signaling coherent motion. The results match many of the known properties of MST cells and are consistent with recent studies indicating that these cells process 3-D object motion information.

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.

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;