How the evolution of air breathing shaped hippocampal function

To make maps from airborne odours requires dynamic respiratory patterns. I propose that this constraint explains the modulation of memory by nasal respiration in mammals, including murine rodents (e.g. laboratory mouse, laboratory rat) and humans. My prior theories of limbic system evolution offer a...

Full description

Bibliographic Details
Published in:Philosophical Transactions of the Royal Society B: Biological Sciences
Main Author: Jacobs, Lucia F.
Other Authors: Radcliffe Institute for Advanced Study, Harvard University, Army Research Office, National Science Foundation
Format: Article in Journal/Newspaper
Language:English
Published: The Royal Society 2021
Subjects:
Online Access:http://dx.doi.org/10.1098/rstb.2020.0532
https://royalsocietypublishing.org/doi/pdf/10.1098/rstb.2020.0532
https://royalsocietypublishing.org/doi/full-xml/10.1098/rstb.2020.0532
id crroyalsociety:10.1098/rstb.2020.0532
record_format openpolar
spelling crroyalsociety:10.1098/rstb.2020.0532 2024-06-02T08:15:17+00:00 How the evolution of air breathing shaped hippocampal function Jacobs, Lucia F. Radcliffe Institute for Advanced Study, Harvard University Army Research Office National Science Foundation 2021 http://dx.doi.org/10.1098/rstb.2020.0532 https://royalsocietypublishing.org/doi/pdf/10.1098/rstb.2020.0532 https://royalsocietypublishing.org/doi/full-xml/10.1098/rstb.2020.0532 en eng The Royal Society https://royalsociety.org/journals/ethics-policies/data-sharing-mining/ Philosophical Transactions of the Royal Society B: Biological Sciences volume 377, issue 1844 ISSN 0962-8436 1471-2970 journal-article 2021 crroyalsociety https://doi.org/10.1098/rstb.2020.0532 2024-05-07T14:16:46Z To make maps from airborne odours requires dynamic respiratory patterns. I propose that this constraint explains the modulation of memory by nasal respiration in mammals, including murine rodents (e.g. laboratory mouse, laboratory rat) and humans. My prior theories of limbic system evolution offer a framework to understand why this occurs. The answer begins with the evolution of nasal respiration in Devonian lobe-finned fishes. This evolutionary innovation led to adaptive radiations in chemosensory systems, including the emergence of the vomeronasal system and a specialization of the main olfactory system for spatial orientation. As mammals continued to radiate into environments hostile to spatial olfaction (air, water), there was a loss of hippocampal structure and function in lineages that evolved sensory modalities adapted to these new environments. Hence the independent evolution of echolocation in bats and toothed whales was accompanied by a loss of hippocampal structure (whales) and an absence of hippocampal theta oscillations during navigation (bats). In conclusion, models of hippocampal function that are divorced from considerations of ecology and evolution fall short of explaining hippocampal diversity across mammals and even hippocampal function in humans. This article is part of the theme issue ‘Systems neuroscience through the lens of evolutionary theory’. Article in Journal/Newspaper toothed whales The Royal Society Philosophical Transactions of the Royal Society B: Biological Sciences 377 1844
institution Open Polar
collection The Royal Society
op_collection_id crroyalsociety
language English
description To make maps from airborne odours requires dynamic respiratory patterns. I propose that this constraint explains the modulation of memory by nasal respiration in mammals, including murine rodents (e.g. laboratory mouse, laboratory rat) and humans. My prior theories of limbic system evolution offer a framework to understand why this occurs. The answer begins with the evolution of nasal respiration in Devonian lobe-finned fishes. This evolutionary innovation led to adaptive radiations in chemosensory systems, including the emergence of the vomeronasal system and a specialization of the main olfactory system for spatial orientation. As mammals continued to radiate into environments hostile to spatial olfaction (air, water), there was a loss of hippocampal structure and function in lineages that evolved sensory modalities adapted to these new environments. Hence the independent evolution of echolocation in bats and toothed whales was accompanied by a loss of hippocampal structure (whales) and an absence of hippocampal theta oscillations during navigation (bats). In conclusion, models of hippocampal function that are divorced from considerations of ecology and evolution fall short of explaining hippocampal diversity across mammals and even hippocampal function in humans. This article is part of the theme issue ‘Systems neuroscience through the lens of evolutionary theory’.
author2 Radcliffe Institute for Advanced Study, Harvard University
Army Research Office
National Science Foundation
format Article in Journal/Newspaper
author Jacobs, Lucia F.
spellingShingle Jacobs, Lucia F.
How the evolution of air breathing shaped hippocampal function
author_facet Jacobs, Lucia F.
author_sort Jacobs, Lucia F.
title How the evolution of air breathing shaped hippocampal function
title_short How the evolution of air breathing shaped hippocampal function
title_full How the evolution of air breathing shaped hippocampal function
title_fullStr How the evolution of air breathing shaped hippocampal function
title_full_unstemmed How the evolution of air breathing shaped hippocampal function
title_sort how the evolution of air breathing shaped hippocampal function
publisher The Royal Society
publishDate 2021
url http://dx.doi.org/10.1098/rstb.2020.0532
https://royalsocietypublishing.org/doi/pdf/10.1098/rstb.2020.0532
https://royalsocietypublishing.org/doi/full-xml/10.1098/rstb.2020.0532
genre toothed whales
genre_facet toothed whales
op_source Philosophical Transactions of the Royal Society B: Biological Sciences
volume 377, issue 1844
ISSN 0962-8436 1471-2970
op_rights https://royalsociety.org/journals/ethics-policies/data-sharing-mining/
op_doi https://doi.org/10.1098/rstb.2020.0532
container_title Philosophical Transactions of the Royal Society B: Biological Sciences
container_volume 377
container_issue 1844
_version_ 1800739397451120640