Are Neural Transactions in the Retina Performed by Phase Ternary Computation?

Author:

Johnson AS ,Winlow W

Abstract

Substantial evidence has accumulated to show that the action potential is always accompanied by a synchronized coupled soliton pressure pulse in the cell membrane, the action potential pulse (APPulse). Furthermore, it has been postulated that, in computational terms, the action potential is a compound ternary structure consisting of two digital phases (the resting potential and the action potential) and a third-time dependent analogue variable, the refractory period. Together, with the APPulse, these phases are described as the computational action potential (CAP), which allows computation by phase. The nature of transmission, and thus computation across membranes, is dependent upon their structures, which have similar components from one neuron to another. Because perception and therefore sentience must be defined by the capabilities of the brain computational model, we propose that phase-ternary mathematics (PTM) is the native mathematical process underlying perception, consciousness and sentience. In this review, we take the CAP concept and apply it to the working of a well-defined neural network, the vertebrate retina. We propose an accurate working computational model of the retina and provide an explanation of computation of the neural transactions within it using PTM, and provide evidence that could form the basis of understanding neural computation within the entire nervous system. Evidence is presented of phase ternary computation (PTC), defined in phase ternary mathematics and shows an exact mathematical correlation between the activity of the amacrine cells, the bipolar cells and ganglion cells of the retina, once these cells have been activated by light falling on the cones. In this model, the computation of luminosity of multiple cones synapsed to a bipolar cell is performed by phase ternary mathematics at the points of convergence of CAPs. Redaction by the refractory periods of converging CAPs eliminates all but the leading APPulse resulting in sampling and averaging. In phase ternary analysis (PTA), the physiology of synapses defines their primary action as latency changers, changing the time taken for impulses to travel between points of convergence. This paper describes a novel type of computation, PTC, with evidence that it is the fundamental computational method used by the retina and by association the rest of the brain. By comparing the morphology of neurons it is now possible to explain their function singly and in networks. This has profound consequences both for our understanding of the brain and in clinical practice.

Publisher

Gratis Open Access Publishers LLC

Cited by 5 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3