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Basal tolerance but not plasticity gives invasive springtails the advantage in an assemblage setting
As global climates change, alien species are anticipated to have a growing advantage relative to their indigenous counterparts, mediated through consistent trait differences between the groups. These insights have largely been developed based on interspecific comparisons using multiple species exami...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7294889/ https://www.ncbi.nlm.nih.gov/pubmed/32577288 http://dx.doi.org/10.1093/conphys/coaa049 |
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author | Phillips, Laura M Aitkenhead, Ian Janion-Scheepers, Charlene King, Catherine K McGeoch, Melodie A Nielsen, Uffe N Terauds, Aleks Liu, W P Amy Chown, Steven L |
author_facet | Phillips, Laura M Aitkenhead, Ian Janion-Scheepers, Charlene King, Catherine K McGeoch, Melodie A Nielsen, Uffe N Terauds, Aleks Liu, W P Amy Chown, Steven L |
author_sort | Phillips, Laura M |
collection | PubMed |
description | As global climates change, alien species are anticipated to have a growing advantage relative to their indigenous counterparts, mediated through consistent trait differences between the groups. These insights have largely been developed based on interspecific comparisons using multiple species examined from different locations. Whether such consistent physiological trait differences are present within assemblages is not well understood, especially for animals. Yet, it is at the assemblage level that interactions play out. Here, we examine whether physiological trait differences observed at the interspecific level are also applicable to assemblages. We focus on the Collembola, an important component of the soil fauna characterized by invasions globally, and five traits related to fitness: critical thermal maximum, minimum and range, desiccation resistance and egg development rate. We test the predictions that the alien component of a local assemblage has greater basal physiological tolerances or higher rates, and more pronounced phenotypic plasticity than the indigenous component. Basal critical thermal maximum, thermal tolerance range, desiccation resistance, optimum temperature for egg development, the rate of development at that optimum and the upper temperature limiting egg hatching success are all significantly higher, on average, for the alien than the indigenous components of the assemblage. Outcomes for critical thermal minimum are variable. No significant differences in phenotypic plasticity exist between the alien and indigenous components of the assemblage. These results are consistent with previous interspecific studies investigating basal thermal tolerance limits and development rates and their phenotypic plasticity, in arthropods, but are inconsistent with results from previous work on desiccation resistance. Thus, for the Collembola, the anticipated advantage of alien over indigenous species under warming and drying is likely to be manifest in local assemblages, globally. |
format | Online Article Text |
id | pubmed-7294889 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-72948892020-06-22 Basal tolerance but not plasticity gives invasive springtails the advantage in an assemblage setting Phillips, Laura M Aitkenhead, Ian Janion-Scheepers, Charlene King, Catherine K McGeoch, Melodie A Nielsen, Uffe N Terauds, Aleks Liu, W P Amy Chown, Steven L Conserv Physiol Research Article As global climates change, alien species are anticipated to have a growing advantage relative to their indigenous counterparts, mediated through consistent trait differences between the groups. These insights have largely been developed based on interspecific comparisons using multiple species examined from different locations. Whether such consistent physiological trait differences are present within assemblages is not well understood, especially for animals. Yet, it is at the assemblage level that interactions play out. Here, we examine whether physiological trait differences observed at the interspecific level are also applicable to assemblages. We focus on the Collembola, an important component of the soil fauna characterized by invasions globally, and five traits related to fitness: critical thermal maximum, minimum and range, desiccation resistance and egg development rate. We test the predictions that the alien component of a local assemblage has greater basal physiological tolerances or higher rates, and more pronounced phenotypic plasticity than the indigenous component. Basal critical thermal maximum, thermal tolerance range, desiccation resistance, optimum temperature for egg development, the rate of development at that optimum and the upper temperature limiting egg hatching success are all significantly higher, on average, for the alien than the indigenous components of the assemblage. Outcomes for critical thermal minimum are variable. No significant differences in phenotypic plasticity exist between the alien and indigenous components of the assemblage. These results are consistent with previous interspecific studies investigating basal thermal tolerance limits and development rates and their phenotypic plasticity, in arthropods, but are inconsistent with results from previous work on desiccation resistance. Thus, for the Collembola, the anticipated advantage of alien over indigenous species under warming and drying is likely to be manifest in local assemblages, globally. Oxford University Press 2020-06-15 /pmc/articles/PMC7294889/ /pubmed/32577288 http://dx.doi.org/10.1093/conphys/coaa049 Text en © The Author(s) 2020. Published by Oxford University Press and the Society for Experimental Biology. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Phillips, Laura M Aitkenhead, Ian Janion-Scheepers, Charlene King, Catherine K McGeoch, Melodie A Nielsen, Uffe N Terauds, Aleks Liu, W P Amy Chown, Steven L Basal tolerance but not plasticity gives invasive springtails the advantage in an assemblage setting |
title | Basal tolerance but not plasticity gives invasive springtails the advantage in an assemblage setting |
title_full | Basal tolerance but not plasticity gives invasive springtails the advantage in an assemblage setting |
title_fullStr | Basal tolerance but not plasticity gives invasive springtails the advantage in an assemblage setting |
title_full_unstemmed | Basal tolerance but not plasticity gives invasive springtails the advantage in an assemblage setting |
title_short | Basal tolerance but not plasticity gives invasive springtails the advantage in an assemblage setting |
title_sort | basal tolerance but not plasticity gives invasive springtails the advantage in an assemblage setting |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7294889/ https://www.ncbi.nlm.nih.gov/pubmed/32577288 http://dx.doi.org/10.1093/conphys/coaa049 |
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