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.

Ni1000 was designed to calculate "city block" distances (Le.

The localization and orientation to various novel or interesting events in the environment is a critical sensorimotor ability in all animals, predator or prey. In mammals, the superior colliculus (SC) plays a major role in this behavior, the deeper layers exhibiting topographically mapped responses to visual, auditory, and somatosensory stimuli. Sensory information arriving from different modalities should then be represented in the same coordinate frame. Auditory cues, in particular, are thought to be computed in head-based coordinates which must then be transformed to retinal coordinates. In this paper, an analog VLSI implementation for auditory localization in the azimuthal plane is described which extends the architecture proposed for the barn owl to a primate eye movement system where further transformation is required. This transformation is intended to model the projection in primates from auditory cortical areas to the deeper layers of the primate superior colliculus. This system is interfaced with an analog VLSI-based saccadic eye movement system also being constructed in our laboratory.

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.

Casting neural network weights in symbolic terms is crucial for interpreting and explaining the behavior of a network. Additionally, in some domains, a symbolic description may lead to more robust generalization. We present a principled approach to symbolic rule extraction based on the notion of weight templates, parameterized regions of weight space corresponding to specific symbolic expressions. With an appropriate choice of representation, we show how template parameters may be efficiently identified and instantiated to yield the optimal match to a unit's actual weights.

MLP networks provided slightly better risk prediction than conventional logistic regression when used to predict the risk of death, stroke, and renal failure on 1257 patients who underwent coronary artery bypass operations. Bootstrap sampling was required to compare approaches and regularization provided by early stopping was an important component of improved performance. A simplified approach to generating confidence intervals for MLP risk predictions using an auxiliary "confidence MLP" was also developed. The confidence MLP is trained to reproduce the confidence bounds that were generated during training by 50 MLP networks trained using bootstrap samples. Current research is validating these results using larger data sets, exploring approaches to detect outlier patients who are so different from any training patient that accurate risk prediction is suspect, developing approaches to explaining which input features are important for an individual patient, and determining why MLP networks provide improved performance.

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.

Such sensors realize the simultaneous need for wide field-of-view and good visual acuity. One popular class of space-variant sensors is formed by log-polar sensors which have a small area near the optical axis of greatly increased resolution (the fovea) coupled with a peripheral region that witnesses a gradual logarithmic falloff in resolution as one moves radially outward. These sensors are inspired by similar structures found in the primate retina where one finds both a peripheral region of gradually decreasing acuity and a circularly symmetric area centmlis characterized by a greater density of receptors and a disproportionate representation in the optic nerve [3]. The peripheral region, though of low visual acuity, is more sensitive to light intensity and movement. The existence of a region optimized for discrimination and recognition surrounded by a region geared towards detection thus allows the image of an object of interest detected in the outer region to be placed on the more analytic center for closer scrutiny. Such a strategy however necessitates the existence of (a) methods to determine which location in the periphery to foveate next, and (b) fast gaze-shifting mechanisms to achieve this 894 Rajesh P. N. Rao, Dana H. Ballard

In supervised learning, learning from queries rather than from random examples can improve generalization performance significantly. We study the performance of query learning for problems where the student cannot learn the teacher perfectly, which occur frequently in practice. As a prototypical scenario of this kind, we consider a linear perceptron student learning a binary perceptron teacher. Two kinds of queries for maximum information gain, i.e., minimum entropy, are investigated: Minimum student space entropy (MSSE) queries, which are appropriate if the teacher space is unknown, and minimum teacher space entropy (MTSE) queries, which can be used if the teacher space is assumed to be known, but a student of a simpler form has deliberately been chosen. We find that for MSSE queries, the structure of the student space determines the efficacy of query learning, whereas MTSE queries lead to a higher generalization error than random examples, due to a lack of feedback about the progress of the student in the way queries are selected.

Experiments were performed to reveal some of the computational properties of the human motor memory system. We show that as humans practice reaching movements while interacting with a novel mechanical environment, they learn an internal model of the inverse dynamics of that environment. The representation of the internal model in memory is such that there is interference when there is an attempt to learn a new inverse dynamics map immediately after an anticorrelated mapping was learned. We suggest that this interference is an indication that the same computational elements used to encode the first inverse dynamics map are being used to learn the second mapping. We predict that this leads to a forgetting of the initially learned skill. 1 Introduction In tasks where we use our hands to interact with a tool, our motor system develops a model of the dynamics of that tool and uses this model to control the coupled dynamics of our arm and the tool (Shadmehr and Mussa-Ivaldi 1994). In physical systems theory, the tool is a mechanical analogue of an admittance, mapping a force as input onto a change in state as output (Hogan 1985).