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Learning the Solution to the Aperture Problem for Pattern Motion with a Hebb Rule
The primate visual system learns to recognize the true direction of pattern motion using local detectors only capable of detecting the component of motion perpendicular to the orientation of the moving edge. A multilayer feedforward network model similar to Linsker's model was presented with input patterns each consisting of randomly oriented contours moving in a particular direction. Input layer units are granted component direction and speed tuning curves similar to those recorded from neurons in primate visual area VI that project to area MT. The network is trained on many such patterns until most weights saturate. A proportion of the units in the second layer solve the aperture problem (e.g., show the same direction-tuning curve peak to plaids as to gratings), resembling pattern-direction selective neurons, which ftrst appear inareaMT.
Temporal Representations in a Connectionist Speech System
Erich J. Smythe 207 Greenmanville Ave, #6 Mystic, CT 06355 ABSTRACT SYREN is a connectionist model that uses temporal information in a speech signal for syllable recognition. It classifies the rates and directions of formant center transitions, and uses an adaptive method to associate transition events with each syllable. The system uses explicit spatial temporal representations through delay lines. SYREN uses implicit parametric temporal representations in formant transition classification through node activation onset, decay, and transition delays in sub-networks analogous to visual motion detector cells. SYREN recognizes 79% of six repetitions of 24 consonant-vowel syllables when tested on unseen data, and recognizes 100% of its training syllables. INTRODUCTION Living organisms exist in a dynamic environment. Problem solving systems, both natural and synthetic, must relate and interpret events that occur over time.
Cricket Wind Detection
A great deal of interest has recently been focused on theories concerning parallel distributed processing in central nervous systems. In particular, many researchers have become very interested in the structure and function of "computational maps" in sensory systems. As defined in a recent review (Knudsen et al, 1987), a "map" is an array of nerve cells, within which there is a systematic variation in the "tuning" of neighboring cells for a particular parameter. For example, the projection from retina to visual cortex is a relatively simple topographic map; each cortical hypercolumn itself contains a more complex "computational" map of preferred line orientation representing the angle of tilt of a simple line stimulus. The overall goal of the research in my lab is to determine how a relatively complex mapped sensory system extracts and encodes information from external stimuli.
Neural Control of Sensory Acquisition: The Vestibulo-Ocular Reflex
Paulin, Michael G., Nelson, Mark E., Bower, James M.
We present a new hypothesis that the cerebellum plays a key role in actively controlling the acquisition of sensory infonnation by the nervous system. In this paper we explore this idea by examining the function of a simple cerebellar-related behavior, the vestibula-ocular reflex or VOR, in which eye movements are generated to minimize image slip on the retina during rapid head movements. Considering this system from the point of view of statistical estimation theory, our results suggest that the transfer function of the VOR, often regarded as a static or slowly modifiable feature of the system, should actually be continuously and rapidly changed during head movements. We further suggest that these changes are under the direct control of the cerebellar cortex and propose experiments to test this hypothesis.
Modeling Small Oscillating Biological Networks in Analog VLSI
Ryckebusch, Sylvie, Bower, James M., Mead, Carver
We have used analog VLSI technology to model a class of small oscillating biological neural circuits known as central pattern generators (CPG). These circuits generate rhythmic patterns of activity which drive locomotor behaviour in the animal. We have designed, fabricated, and tested a model neuron circuit which relies on many of the same mechanisms as a biological central pattern generator neuron, such as delays and internal feedback. We show that this neuron can be used to build several small circuits based on known biological CPG circuits, and that these circuits produce patterns of output which are very similar to the observed biological patterns. To date, researchers in applied neural networks have tended to focus on mammalian systems as the primary source of potentially useful biological information. However, invertebrate systems may represent a source of ideas in many ways more appropriate, given current levels of engineering sophistication in building neural-like systems, and given the state of biological understanding of mammalian circuits.
Storing Covariance by the Associative Long-Term Potentiation and Depression of Synaptic Strengths in the Hippocampus
Stanton, Patric K., Sejnowski, Terrence J.
We have tested this assumption in the hippocampus, a cortical structure or the brain that is involved in long-term memory. A brier, high-frequency activation or excitatory synapses in the hippocampus produces an increase in synaptic strength known as long-term potentiation, or L TP (BUss and Lomo, 1973), that can last ror many days. LTP is known to be Hebbian since it requires the simultaneous release or neurotransmitter from presynaptic terminals coupled with postsynaptic depolarization (Kelso et al, 1986; Malinow and Miller, 1986; Gustatrson et al, 1987). However, a mechanism ror the persistent reduction or synaptic strength that could balance LTP has not yet been demonstrated. We studied the associative interactions between separate inputs onto the same dendritic trees or hippocampal pyramidal cells or field CAl, and round that a low-frequency input which, by itselr, does not persistently change synaptic strength, can either increase (associative L TP) or decrease in strength (associative long-term depression or LTD) depending upon whether it is positively or negatively correlated in time with a second, high-frequency bursting input. LTP or synaptic strength is Hebbian, and LTD is anti-Hebbian since it is elicited by pairing presynaptic firing with postsynaptic hyperpolarization sufficient to block postsynaptic activity.
Efficient Parallel Learning Algorithms for Neural Networks
Kramer, Alan H., Sangiovanni-Vincentelli, Alberto
Parallelizable optimization techniques are applied to the problem of learning in feedforward neural networks. In addition to having superior convergence properties, optimization techniques such as the Polak Ribiere method are also significantly more efficient than the Backpropagation algorithm. These results are based on experiments performed on small boolean learning problems and the noisy real-valued learning problem of handwritten character recognition. 1 INTRODUCTION The problem of learning in feedforward neural networks has received a great deal of attention recently because of the ability of these networks to represent seemingly complex mappings in an efficient parallel architecture. This learning problem can be characterized as an optimization problem, but it is unique in several respects. Function evaluation is very expensive. However, because the underlying network is parallel in nature, this evaluation is easily parallelizable.
Models of Ocular Dominance Column Formation: Analytical and Computational Results
Miller, Kenneth D., Keller, Joseph B., Stryker, Michael P.
In the developing visual system in many mammalian species, there is initially a uniform, overlapping innervation of layer 4 of the visual cortex by inputs representing the two eyes. Subsequently, these inputs segregate into patches or stripes that are largely or exclusively innervated by inputs serving a single eye, known as ocular dominance patches. The ocular dominance patches are on a small scale compared to the map of the visual world, so that the initially continuous map becomes two interdigitated maps, one representing each eye. These patches, together with the layers of cortex above and below layer 4, whose responses are dominated by the eye innervating the corresponding layer 4 patch, are known as ocular dominance columns.