Cargando…

Prospecting movements link phenotypic traits to female annual potential fitness in a nocturnal predator

Recent biologging technology reveals hidden life and breeding strategies of nocturnal animals. Combining animal movement patterns with individual characteristics and landscape features can uncover meaningful behaviours that directly influence fitness. Consequently, defining the proximate mechanisms...

Descripción completa

Detalles Bibliográficos
Autores principales: Becciu, Paolo, Séchaud, Robin, Schalcher, Kim, Plancherel, Céline, Roulin, Alexandre
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10050157/
https://www.ncbi.nlm.nih.gov/pubmed/36977731
http://dx.doi.org/10.1038/s41598-023-32255-7
_version_ 1785014606442266624
author Becciu, Paolo
Séchaud, Robin
Schalcher, Kim
Plancherel, Céline
Roulin, Alexandre
author_facet Becciu, Paolo
Séchaud, Robin
Schalcher, Kim
Plancherel, Céline
Roulin, Alexandre
author_sort Becciu, Paolo
collection PubMed
description Recent biologging technology reveals hidden life and breeding strategies of nocturnal animals. Combining animal movement patterns with individual characteristics and landscape features can uncover meaningful behaviours that directly influence fitness. Consequently, defining the proximate mechanisms and adaptive value of the identified behaviours is of paramount importance. Breeding female barn owls (Tyto alba), a colour-polymorphic species, recurrently visit other nest boxes at night. We described and quantified this behaviour for the first time, linking it with possible drivers, and individual fitness. We GPS-equipped 178 female barn owls and 122 male partners from 2016 to 2020 in western Switzerland during the chick rearing phase. We observed that 111 (65%) of the tracked breeding females were (re)visiting nest boxes while still carrying out their first brood. We modelled their prospecting parameters as a function of brood-, individual- and partner-related variables and found that female feather eumelanism predicted the emergence of prospecting behaviour (less melanic females are usually prospecting). More importantly we found that increasing male parental investment (e.g., feeding rate) increased female prospecting efforts. Ultimately, females would (re)visit a nest more often if they had used it in the past and were more likely to lay a second clutch afterwards, consequently having higher annual fecundity than non-prospecting females. Despite these apparent immediate benefits, they did not fledge more chicks. Through biologging and long-term field monitoring, we highlight how phenotypic traits (melanism and parental investment) can be related to movement patterns and the annual potential reproductive output (fecundity) of female barn owls.
format Online
Article
Text
id pubmed-10050157
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-100501572023-03-30 Prospecting movements link phenotypic traits to female annual potential fitness in a nocturnal predator Becciu, Paolo Séchaud, Robin Schalcher, Kim Plancherel, Céline Roulin, Alexandre Sci Rep Article Recent biologging technology reveals hidden life and breeding strategies of nocturnal animals. Combining animal movement patterns with individual characteristics and landscape features can uncover meaningful behaviours that directly influence fitness. Consequently, defining the proximate mechanisms and adaptive value of the identified behaviours is of paramount importance. Breeding female barn owls (Tyto alba), a colour-polymorphic species, recurrently visit other nest boxes at night. We described and quantified this behaviour for the first time, linking it with possible drivers, and individual fitness. We GPS-equipped 178 female barn owls and 122 male partners from 2016 to 2020 in western Switzerland during the chick rearing phase. We observed that 111 (65%) of the tracked breeding females were (re)visiting nest boxes while still carrying out their first brood. We modelled their prospecting parameters as a function of brood-, individual- and partner-related variables and found that female feather eumelanism predicted the emergence of prospecting behaviour (less melanic females are usually prospecting). More importantly we found that increasing male parental investment (e.g., feeding rate) increased female prospecting efforts. Ultimately, females would (re)visit a nest more often if they had used it in the past and were more likely to lay a second clutch afterwards, consequently having higher annual fecundity than non-prospecting females. Despite these apparent immediate benefits, they did not fledge more chicks. Through biologging and long-term field monitoring, we highlight how phenotypic traits (melanism and parental investment) can be related to movement patterns and the annual potential reproductive output (fecundity) of female barn owls. Nature Publishing Group UK 2023-03-28 /pmc/articles/PMC10050157/ /pubmed/36977731 http://dx.doi.org/10.1038/s41598-023-32255-7 Text en © The Author(s) 2023 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
Becciu, Paolo
Séchaud, Robin
Schalcher, Kim
Plancherel, Céline
Roulin, Alexandre
Prospecting movements link phenotypic traits to female annual potential fitness in a nocturnal predator
title Prospecting movements link phenotypic traits to female annual potential fitness in a nocturnal predator
title_full Prospecting movements link phenotypic traits to female annual potential fitness in a nocturnal predator
title_fullStr Prospecting movements link phenotypic traits to female annual potential fitness in a nocturnal predator
title_full_unstemmed Prospecting movements link phenotypic traits to female annual potential fitness in a nocturnal predator
title_short Prospecting movements link phenotypic traits to female annual potential fitness in a nocturnal predator
title_sort prospecting movements link phenotypic traits to female annual potential fitness in a nocturnal predator
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10050157/
https://www.ncbi.nlm.nih.gov/pubmed/36977731
http://dx.doi.org/10.1038/s41598-023-32255-7
work_keys_str_mv AT becciupaolo prospectingmovementslinkphenotypictraitstofemaleannualpotentialfitnessinanocturnalpredator
AT sechaudrobin prospectingmovementslinkphenotypictraitstofemaleannualpotentialfitnessinanocturnalpredator
AT schalcherkim prospectingmovementslinkphenotypictraitstofemaleannualpotentialfitnessinanocturnalpredator
AT plancherelceline prospectingmovementslinkphenotypictraitstofemaleannualpotentialfitnessinanocturnalpredator
AT roulinalexandre prospectingmovementslinkphenotypictraitstofemaleannualpotentialfitnessinanocturnalpredator