Cargando…
The efference cascade, consciousness, and its self: naturalizing the first person pivot of action control
The 20 billion neurons of the neocortex have a mere hundred thousand motor neurons by which to express cortical contents in overt behavior. Implemented through a staggered cortical “efference cascade” originating in the descending axons of layer five pyramidal cells throughout the neocortical expans...
Autor principal: | |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2013
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3738861/ https://www.ncbi.nlm.nih.gov/pubmed/23950750 http://dx.doi.org/10.3389/fpsyg.2013.00501 |
_version_ | 1782476889454018560 |
---|---|
author | Merker, Bjorn |
author_facet | Merker, Bjorn |
author_sort | Merker, Bjorn |
collection | PubMed |
description | The 20 billion neurons of the neocortex have a mere hundred thousand motor neurons by which to express cortical contents in overt behavior. Implemented through a staggered cortical “efference cascade” originating in the descending axons of layer five pyramidal cells throughout the neocortical expanse, this steep convergence accomplishes final integration for action of cortical information through a system of interconnected subcortical way stations. Coherent and effective action control requires the inclusion of a continually updated joint “global best estimate” of current sensory, motivational, and motor circumstances in this process. I have previously proposed that this running best estimate is extracted from cortical probabilistic preliminaries by a subcortical neural “reality model” implementing our conscious sensory phenomenology. As such it must exhibit first person perspectival organization, suggested to derive from formating requirements of the brain's subsystem for gaze control, with the superior colliculus at its base. Gaze movements provide the leading edge of behavior by capturing targets of engagement prior to contact. The rotation-based geometry of directional gaze movements places their implicit origin inside the head, a location recoverable by cortical probabilistic source reconstruction from the rampant primary sensory variance generated by the incessant play of collicularly triggered gaze movements. At the interface between cortex and colliculus lies the dorsal pulvinar. Its unique long-range inhibitory circuitry may precipitate the brain's global best estimate of its momentary circumstances through multiple constraint satisfaction across its afferents from numerous cortical areas and colliculus. As phenomenal content of our sensory awareness, such a global best estimate would exhibit perspectival organization centered on a purely implicit first person origin, inherently incapable of appearing as a phenomenal content of the sensory space it serves. |
format | Online Article Text |
id | pubmed-3738861 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-37388612013-08-15 The efference cascade, consciousness, and its self: naturalizing the first person pivot of action control Merker, Bjorn Front Psychol Psychology The 20 billion neurons of the neocortex have a mere hundred thousand motor neurons by which to express cortical contents in overt behavior. Implemented through a staggered cortical “efference cascade” originating in the descending axons of layer five pyramidal cells throughout the neocortical expanse, this steep convergence accomplishes final integration for action of cortical information through a system of interconnected subcortical way stations. Coherent and effective action control requires the inclusion of a continually updated joint “global best estimate” of current sensory, motivational, and motor circumstances in this process. I have previously proposed that this running best estimate is extracted from cortical probabilistic preliminaries by a subcortical neural “reality model” implementing our conscious sensory phenomenology. As such it must exhibit first person perspectival organization, suggested to derive from formating requirements of the brain's subsystem for gaze control, with the superior colliculus at its base. Gaze movements provide the leading edge of behavior by capturing targets of engagement prior to contact. The rotation-based geometry of directional gaze movements places their implicit origin inside the head, a location recoverable by cortical probabilistic source reconstruction from the rampant primary sensory variance generated by the incessant play of collicularly triggered gaze movements. At the interface between cortex and colliculus lies the dorsal pulvinar. Its unique long-range inhibitory circuitry may precipitate the brain's global best estimate of its momentary circumstances through multiple constraint satisfaction across its afferents from numerous cortical areas and colliculus. As phenomenal content of our sensory awareness, such a global best estimate would exhibit perspectival organization centered on a purely implicit first person origin, inherently incapable of appearing as a phenomenal content of the sensory space it serves. Frontiers Media S.A. 2013-08-09 /pmc/articles/PMC3738861/ /pubmed/23950750 http://dx.doi.org/10.3389/fpsyg.2013.00501 Text en Copyright © 2013 Merker. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Psychology Merker, Bjorn The efference cascade, consciousness, and its self: naturalizing the first person pivot of action control |
title | The efference cascade, consciousness, and its self: naturalizing the first person pivot of action control |
title_full | The efference cascade, consciousness, and its self: naturalizing the first person pivot of action control |
title_fullStr | The efference cascade, consciousness, and its self: naturalizing the first person pivot of action control |
title_full_unstemmed | The efference cascade, consciousness, and its self: naturalizing the first person pivot of action control |
title_short | The efference cascade, consciousness, and its self: naturalizing the first person pivot of action control |
title_sort | efference cascade, consciousness, and its self: naturalizing the first person pivot of action control |
topic | Psychology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3738861/ https://www.ncbi.nlm.nih.gov/pubmed/23950750 http://dx.doi.org/10.3389/fpsyg.2013.00501 |
work_keys_str_mv | AT merkerbjorn theefferencecascadeconsciousnessanditsselfnaturalizingthefirstpersonpivotofactioncontrol AT merkerbjorn efferencecascadeconsciousnessanditsselfnaturalizingthefirstpersonpivotofactioncontrol |