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Scaling up from greenhouse resistance to fitness in the field for a host of an emerging forest disease
Forest systems are increasingly threatened by emergent, exotic diseases, yet management strategies for forest trees may be hindered by long generation times and scant background knowledge. We tested whether nursery disease resistance and growth traits have predictive value for the conservation of No...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Blackwell Publishing Ltd
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3779097/ https://www.ncbi.nlm.nih.gov/pubmed/24062805 http://dx.doi.org/10.1111/eva.12080 |
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author | Hayden, Katherine J Garbelotto, Matteo Dodd, Richard Wright, Jessica W |
author_facet | Hayden, Katherine J Garbelotto, Matteo Dodd, Richard Wright, Jessica W |
author_sort | Hayden, Katherine J |
collection | PubMed |
description | Forest systems are increasingly threatened by emergent, exotic diseases, yet management strategies for forest trees may be hindered by long generation times and scant background knowledge. We tested whether nursery disease resistance and growth traits have predictive value for the conservation of Notholithocarpus densiflorus, the host most susceptible to sudden oak death. We established three experimental populations to assess nursery growth and resistance to Phytophthora ramorum, and correlations between nursery-derived breeding values with seedling survival in a field disease trial. Estimates of nursery traits’ heritability were low to moderate, with lowest estimates for resistance traits. Within the field trial, survival likelihood was increased in larger seedlings and decreased with the development of disease symptoms. The seed-parent family wide likelihood of survival was likewise correlated with family predictors for size and resistance to disease in 2nd year laboratory assays, though not resistance in 1st year leaf assays. We identified traits and seedling families with increased survivorship in planted tanoaks, and a framework to further identify seed parents favored for restoration. The additive genetic variation and seedling disease dynamics we describe hold promise to refine current disease models and expand the understanding of evolutionary dynamics of emergent infectious diseases in highly susceptible hosts. |
format | Online Article Text |
id | pubmed-3779097 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Blackwell Publishing Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-37790972013-09-23 Scaling up from greenhouse resistance to fitness in the field for a host of an emerging forest disease Hayden, Katherine J Garbelotto, Matteo Dodd, Richard Wright, Jessica W Evol Appl Original Articles Forest systems are increasingly threatened by emergent, exotic diseases, yet management strategies for forest trees may be hindered by long generation times and scant background knowledge. We tested whether nursery disease resistance and growth traits have predictive value for the conservation of Notholithocarpus densiflorus, the host most susceptible to sudden oak death. We established three experimental populations to assess nursery growth and resistance to Phytophthora ramorum, and correlations between nursery-derived breeding values with seedling survival in a field disease trial. Estimates of nursery traits’ heritability were low to moderate, with lowest estimates for resistance traits. Within the field trial, survival likelihood was increased in larger seedlings and decreased with the development of disease symptoms. The seed-parent family wide likelihood of survival was likewise correlated with family predictors for size and resistance to disease in 2nd year laboratory assays, though not resistance in 1st year leaf assays. We identified traits and seedling families with increased survivorship in planted tanoaks, and a framework to further identify seed parents favored for restoration. The additive genetic variation and seedling disease dynamics we describe hold promise to refine current disease models and expand the understanding of evolutionary dynamics of emergent infectious diseases in highly susceptible hosts. Blackwell Publishing Ltd 2013-09 2013-07-19 /pmc/articles/PMC3779097/ /pubmed/24062805 http://dx.doi.org/10.1111/eva.12080 Text en © 2013 The Authors. Evolutionary Applications published by John Wiley & Sons Ltd http://creativecommons.org/licenses/by/2.5/ Re-use of this article is permitted in accordance with the Creative Commons Deed, Attribution 2.5, which does not permit commercial exploitation. |
spellingShingle | Original Articles Hayden, Katherine J Garbelotto, Matteo Dodd, Richard Wright, Jessica W Scaling up from greenhouse resistance to fitness in the field for a host of an emerging forest disease |
title | Scaling up from greenhouse resistance to fitness in the field for a host of an emerging forest disease |
title_full | Scaling up from greenhouse resistance to fitness in the field for a host of an emerging forest disease |
title_fullStr | Scaling up from greenhouse resistance to fitness in the field for a host of an emerging forest disease |
title_full_unstemmed | Scaling up from greenhouse resistance to fitness in the field for a host of an emerging forest disease |
title_short | Scaling up from greenhouse resistance to fitness in the field for a host of an emerging forest disease |
title_sort | scaling up from greenhouse resistance to fitness in the field for a host of an emerging forest disease |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3779097/ https://www.ncbi.nlm.nih.gov/pubmed/24062805 http://dx.doi.org/10.1111/eva.12080 |
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