Cargando…

Kea (Nestor notabilis) fail a loose-string connectivity task

Naïve individuals of some bird species can rapidly solve vertical string-pulling tasks with virtually no errors. This has led to various hypotheses being proposed which suggest that birds mentally simulate the effects of their actions on strings. A competing embodied cognition hypothesis proposes th...

Descripción completa

Detalles Bibliográficos
Autores principales: Bastos, Amalia P. M., Wood, Patrick M., Taylor, Alex H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8322428/
https://www.ncbi.nlm.nih.gov/pubmed/34326392
http://dx.doi.org/10.1038/s41598-021-94879-x
_version_ 1783731045108023296
author Bastos, Amalia P. M.
Wood, Patrick M.
Taylor, Alex H.
author_facet Bastos, Amalia P. M.
Wood, Patrick M.
Taylor, Alex H.
author_sort Bastos, Amalia P. M.
collection PubMed
description Naïve individuals of some bird species can rapidly solve vertical string-pulling tasks with virtually no errors. This has led to various hypotheses being proposed which suggest that birds mentally simulate the effects of their actions on strings. A competing embodied cognition hypothesis proposes that this behaviour is instead modulated by perceptual-motor feedback loops, where feedback of the reward moving closer acts as an internal motivator for functional behaviours, such as pull-stepping. To date, the kea parrot has produced some of the best performances of any bird species at string-pulling tasks. Here, we tested the predictions of the four leading hypotheses for the cognition underpinning bird string-pulling by presenting kea with a horizontal connectivity task where only one of two loose strings was connected to the reward, both before and after receiving perceptual-motor feedback experience. We find that kea fail the connectivity task both before and after perceptual-motor feedback experience, suggesting not only that kea do not mentally simulate their string-pulling actions, but also that perceptual-motor feedback alone is insufficient in eliciting successful performance in the horizontal connectivity task. This suggests a more complex interplay of cognitive factors underlies this iconic example of animal problem-solving.
format Online
Article
Text
id pubmed-8322428
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-83224282021-07-30 Kea (Nestor notabilis) fail a loose-string connectivity task Bastos, Amalia P. M. Wood, Patrick M. Taylor, Alex H. Sci Rep Article Naïve individuals of some bird species can rapidly solve vertical string-pulling tasks with virtually no errors. This has led to various hypotheses being proposed which suggest that birds mentally simulate the effects of their actions on strings. A competing embodied cognition hypothesis proposes that this behaviour is instead modulated by perceptual-motor feedback loops, where feedback of the reward moving closer acts as an internal motivator for functional behaviours, such as pull-stepping. To date, the kea parrot has produced some of the best performances of any bird species at string-pulling tasks. Here, we tested the predictions of the four leading hypotheses for the cognition underpinning bird string-pulling by presenting kea with a horizontal connectivity task where only one of two loose strings was connected to the reward, both before and after receiving perceptual-motor feedback experience. We find that kea fail the connectivity task both before and after perceptual-motor feedback experience, suggesting not only that kea do not mentally simulate their string-pulling actions, but also that perceptual-motor feedback alone is insufficient in eliciting successful performance in the horizontal connectivity task. This suggests a more complex interplay of cognitive factors underlies this iconic example of animal problem-solving. Nature Publishing Group UK 2021-07-29 /pmc/articles/PMC8322428/ /pubmed/34326392 http://dx.doi.org/10.1038/s41598-021-94879-x Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Bastos, Amalia P. M.
Wood, Patrick M.
Taylor, Alex H.
Kea (Nestor notabilis) fail a loose-string connectivity task
title Kea (Nestor notabilis) fail a loose-string connectivity task
title_full Kea (Nestor notabilis) fail a loose-string connectivity task
title_fullStr Kea (Nestor notabilis) fail a loose-string connectivity task
title_full_unstemmed Kea (Nestor notabilis) fail a loose-string connectivity task
title_short Kea (Nestor notabilis) fail a loose-string connectivity task
title_sort kea (nestor notabilis) fail a loose-string connectivity task
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8322428/
https://www.ncbi.nlm.nih.gov/pubmed/34326392
http://dx.doi.org/10.1038/s41598-021-94879-x
work_keys_str_mv AT bastosamaliapm keanestornotabilisfailaloosestringconnectivitytask
AT woodpatrickm keanestornotabilisfailaloosestringconnectivitytask
AT tayloralexh keanestornotabilisfailaloosestringconnectivitytask