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Research Seminar - April 3, 2001
Seminar Announcement
| Title: |
A Parallel Artificial Neural Network Modeling Electrical Nonsynaptic
Communication in the Lamina Ganglionaris of Musca Domestica
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| Speaker: |
Dr Karen Haines
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| |
Department of Electrical and Computing Engineering
Albuquerque High Performance Computing Center
University of New Mexico
and
Maui High Performance Computing Center
Kehei, Maui
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| Date: |
Tuesday 3rd April, 2001 |
| Time: |
4.00pm |
| Venue: |
Room 2.28 |
Abstract
This discussion will consider how electrical nonsynaptic
communication can influence aspects of neural processing. The
research presented proposes that the extracellular space (ECS)
surrounding a collection of neurons maintains an electrical potential
resulting from currents produced by the axons of these neurons. For
the exploration of electrical nonsynaptic communication and its
functionality, an artificial neural network (ANN), which is inspired
by the fly's early visual processing system, was developed.
As with the fly's lamina, the ANN is a hexagonal array of artificial
synaptic cartridges (ALCs). Each ALC maintains an artificial
extracellular space (AECS) potential produced by currents from the
stimulus-receiving artificial neurons, called artificial
photoreceptors (ARs). The ANN applies diffusive mechanisms to model
electrical nonsynaptic communication. Aspects of electrical
nonsynaptic communication included diffusive interactions between the
ARs and their respective AECS as well as between adjacent ALCs. It
will be shown that this arrangement of nonsynaptic channels produces
an intercellular route linking ALCs. Consequently, the AR potential
in one ALC can affect the AECS potential in adjacent ALCs.
As each synaptic cartridge in the fly's lamina contains two large,
second-in-order processing neurons, called large monopolar cells
(LMCs), the ANN also includes two artificial large monopolar cells
(ALMCs). The ALMC receive inputs from six ARs, each with a distinct
visual field. The consideration of how the AECS potential may affect
the input into each ALMC, led to potential differencing input. Thus,
ALMC inputs rely on AR-AECS potential differences. Results presented
will demonstrate that potential differencing reduces the background
potential present in the input potentials. It will also be
demonstrated that potential input differencing results in inputs with
on-center off-surround characteristics.
Although the ANN is a simplification of the fly's lamina, this
research will also demonstrate that biological mechanisms can be
investigated using simpler computational models. To investigate
nonsynaptic mechanisms possibly occurring within the fly's early
visual processing, a computer model for the ANN was developed,
tested, and analyzed. The ANN is computationally expensive. To
improve the performance of the computer program, parallel programming
methods were applied to the computer model. Parallel programming
methods and performance measurements will be discussed.
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