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Ecology and genetics affect relative invasion success of two Echium species in southern Australia

Echium plantagineum and E. vulgare are congeneric exotics first introduced to Australia in the early 1800 s. There, E. plantagineum is now highly invasive, whereas E. vulgare has a limited distribution. Studies were conducted to evaluate distribution, ecology, genetics and secondary chemistry to she...

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Autores principales: Zhu, Xiaocheng, Weston, Paul A., Skoneczny, Dominik, Gopurenko, David, Meyer, Lucie, Lepschi, Brendan J., Callaway, Ragan M., Gurr, Geoff M., Weston, Leslie A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5314367/
https://www.ncbi.nlm.nih.gov/pubmed/28211478
http://dx.doi.org/10.1038/srep42792
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author Zhu, Xiaocheng
Weston, Paul A.
Skoneczny, Dominik
Gopurenko, David
Meyer, Lucie
Lepschi, Brendan J.
Callaway, Ragan M.
Gurr, Geoff M.
Weston, Leslie A.
author_facet Zhu, Xiaocheng
Weston, Paul A.
Skoneczny, Dominik
Gopurenko, David
Meyer, Lucie
Lepschi, Brendan J.
Callaway, Ragan M.
Gurr, Geoff M.
Weston, Leslie A.
author_sort Zhu, Xiaocheng
collection PubMed
description Echium plantagineum and E. vulgare are congeneric exotics first introduced to Australia in the early 1800 s. There, E. plantagineum is now highly invasive, whereas E. vulgare has a limited distribution. Studies were conducted to evaluate distribution, ecology, genetics and secondary chemistry to shed light on factors associated with their respective invasive success. When sampled across geographically diverse locales, E. plantagineum was widespread and exhibited a small genome size (1 C = 0.34 pg), an annual life cycle, and greater genetic diversity as assessed by DNA sequence analysis. It was found frequently in areas with temperature extremes and low rainfall. In contrast, E. vulgare exhibited a larger genome size (1 C = 0.43 pg), a perennial lifecycle, less chloroplast genetic diversity, and occurred in areas with lower temperatures and higher rainfall. Twelve chloroplast haplotypes of E. plantagineum were evident and incidence aligned well with reported historical introduction events. In contrast, E. vulgare exhibited two haplotypes and was found only sporadically at higher elevations. Echium plantagineum possessed significantly higher levels of numerous pyrrolizidine alkaloids involved in plant defence. We conclude that elevated genetic diversity, tolerance to environmental stress and capacity for producing defensive secondary metabolites have contributed to the successful invasion of E. plantagineum in Australia.
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spelling pubmed-53143672017-02-24 Ecology and genetics affect relative invasion success of two Echium species in southern Australia Zhu, Xiaocheng Weston, Paul A. Skoneczny, Dominik Gopurenko, David Meyer, Lucie Lepschi, Brendan J. Callaway, Ragan M. Gurr, Geoff M. Weston, Leslie A. Sci Rep Article Echium plantagineum and E. vulgare are congeneric exotics first introduced to Australia in the early 1800 s. There, E. plantagineum is now highly invasive, whereas E. vulgare has a limited distribution. Studies were conducted to evaluate distribution, ecology, genetics and secondary chemistry to shed light on factors associated with their respective invasive success. When sampled across geographically diverse locales, E. plantagineum was widespread and exhibited a small genome size (1 C = 0.34 pg), an annual life cycle, and greater genetic diversity as assessed by DNA sequence analysis. It was found frequently in areas with temperature extremes and low rainfall. In contrast, E. vulgare exhibited a larger genome size (1 C = 0.43 pg), a perennial lifecycle, less chloroplast genetic diversity, and occurred in areas with lower temperatures and higher rainfall. Twelve chloroplast haplotypes of E. plantagineum were evident and incidence aligned well with reported historical introduction events. In contrast, E. vulgare exhibited two haplotypes and was found only sporadically at higher elevations. Echium plantagineum possessed significantly higher levels of numerous pyrrolizidine alkaloids involved in plant defence. We conclude that elevated genetic diversity, tolerance to environmental stress and capacity for producing defensive secondary metabolites have contributed to the successful invasion of E. plantagineum in Australia. Nature Publishing Group 2017-02-17 /pmc/articles/PMC5314367/ /pubmed/28211478 http://dx.doi.org/10.1038/srep42792 Text en Copyright © 2017, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Zhu, Xiaocheng
Weston, Paul A.
Skoneczny, Dominik
Gopurenko, David
Meyer, Lucie
Lepschi, Brendan J.
Callaway, Ragan M.
Gurr, Geoff M.
Weston, Leslie A.
Ecology and genetics affect relative invasion success of two Echium species in southern Australia
title Ecology and genetics affect relative invasion success of two Echium species in southern Australia
title_full Ecology and genetics affect relative invasion success of two Echium species in southern Australia
title_fullStr Ecology and genetics affect relative invasion success of two Echium species in southern Australia
title_full_unstemmed Ecology and genetics affect relative invasion success of two Echium species in southern Australia
title_short Ecology and genetics affect relative invasion success of two Echium species in southern Australia
title_sort ecology and genetics affect relative invasion success of two echium species in southern australia
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5314367/
https://www.ncbi.nlm.nih.gov/pubmed/28211478
http://dx.doi.org/10.1038/srep42792
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