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Intermediate predator naïveté and sex-skewed vulnerability predict the impact of an invasive higher predator

The spread of invasive species continues to reduce biodiversity across all regions and habitat types globally. However, invader impact prediction can be nebulous, and approaches often fail to integrate coupled direct and indirect invader effects. Here, we examine the ecological impacts of an invasiv...

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Autores principales: Cuthbert, Ross N., Dalu, Tatenda, Wasserman, Ryan J., Dick, Jaimie T. A., Mofu, Lubabalo, Callaghan, Amanda, Weyl, Olaf L. F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6155278/
https://www.ncbi.nlm.nih.gov/pubmed/30250163
http://dx.doi.org/10.1038/s41598-018-32728-0
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author Cuthbert, Ross N.
Dalu, Tatenda
Wasserman, Ryan J.
Dick, Jaimie T. A.
Mofu, Lubabalo
Callaghan, Amanda
Weyl, Olaf L. F.
author_facet Cuthbert, Ross N.
Dalu, Tatenda
Wasserman, Ryan J.
Dick, Jaimie T. A.
Mofu, Lubabalo
Callaghan, Amanda
Weyl, Olaf L. F.
author_sort Cuthbert, Ross N.
collection PubMed
description The spread of invasive species continues to reduce biodiversity across all regions and habitat types globally. However, invader impact prediction can be nebulous, and approaches often fail to integrate coupled direct and indirect invader effects. Here, we examine the ecological impacts of an invasive higher predator on lower trophic groups, further developing methodologies to more holistically quantify invader impact. We employ functional response (FR, resource use under different densities) and prey switching experiments to examine the trait- and density-mediated impacts of the invasive mosquitofish Gambusia affinis on an endemic intermediate predator Lovenula raynerae (Copepoda). Lovenula raynerae effectively consumed larval mosquitoes, but was naïve to mosquitofish cues, with attack rates and handling times of the intermediate predator unaffected by mosquitofish cue-treated water. Mosquitofish did not switch between male and female prey, consistently displaying a strong preference for female copepods. We thus demonstrate a lack of risk-reduction activity in the presence of invasive fish by L. raynerae and, in turn, high susceptibility of such intermediate trophic groups to invader impact. Further, we show that mosquitofish demonstrate sex-skewed predator selectivity towards intermediate predators of mosquito larvae, which may affect predator population demographics and, perversely, increase disease vector proliferations. We advocate the utility of FRs and prey switching combined to holistically quantify invasive species impact potential on native organisms at multiple trophic levels.
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spelling pubmed-61552782018-09-28 Intermediate predator naïveté and sex-skewed vulnerability predict the impact of an invasive higher predator Cuthbert, Ross N. Dalu, Tatenda Wasserman, Ryan J. Dick, Jaimie T. A. Mofu, Lubabalo Callaghan, Amanda Weyl, Olaf L. F. Sci Rep Article The spread of invasive species continues to reduce biodiversity across all regions and habitat types globally. However, invader impact prediction can be nebulous, and approaches often fail to integrate coupled direct and indirect invader effects. Here, we examine the ecological impacts of an invasive higher predator on lower trophic groups, further developing methodologies to more holistically quantify invader impact. We employ functional response (FR, resource use under different densities) and prey switching experiments to examine the trait- and density-mediated impacts of the invasive mosquitofish Gambusia affinis on an endemic intermediate predator Lovenula raynerae (Copepoda). Lovenula raynerae effectively consumed larval mosquitoes, but was naïve to mosquitofish cues, with attack rates and handling times of the intermediate predator unaffected by mosquitofish cue-treated water. Mosquitofish did not switch between male and female prey, consistently displaying a strong preference for female copepods. We thus demonstrate a lack of risk-reduction activity in the presence of invasive fish by L. raynerae and, in turn, high susceptibility of such intermediate trophic groups to invader impact. Further, we show that mosquitofish demonstrate sex-skewed predator selectivity towards intermediate predators of mosquito larvae, which may affect predator population demographics and, perversely, increase disease vector proliferations. We advocate the utility of FRs and prey switching combined to holistically quantify invasive species impact potential on native organisms at multiple trophic levels. Nature Publishing Group UK 2018-09-24 /pmc/articles/PMC6155278/ /pubmed/30250163 http://dx.doi.org/10.1038/s41598-018-32728-0 Text en © The Author(s) 2018 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Cuthbert, Ross N.
Dalu, Tatenda
Wasserman, Ryan J.
Dick, Jaimie T. A.
Mofu, Lubabalo
Callaghan, Amanda
Weyl, Olaf L. F.
Intermediate predator naïveté and sex-skewed vulnerability predict the impact of an invasive higher predator
title Intermediate predator naïveté and sex-skewed vulnerability predict the impact of an invasive higher predator
title_full Intermediate predator naïveté and sex-skewed vulnerability predict the impact of an invasive higher predator
title_fullStr Intermediate predator naïveté and sex-skewed vulnerability predict the impact of an invasive higher predator
title_full_unstemmed Intermediate predator naïveté and sex-skewed vulnerability predict the impact of an invasive higher predator
title_short Intermediate predator naïveté and sex-skewed vulnerability predict the impact of an invasive higher predator
title_sort intermediate predator naïveté and sex-skewed vulnerability predict the impact of an invasive higher predator
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6155278/
https://www.ncbi.nlm.nih.gov/pubmed/30250163
http://dx.doi.org/10.1038/s41598-018-32728-0
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