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Evaluating β Diversity as a Surrogate for Species Representation at Fine Scale
Species turnover or β diversity is a conceptually attractive surrogate for conservation planning. However, there has been only 1 attempt to determine how well sites selected to maximize β diversity represent species, and that test was done at a scale too coarse (2,500 km(2) sites) to inform most con...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Public Library of Science
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4778865/ https://www.ncbi.nlm.nih.gov/pubmed/26943170 http://dx.doi.org/10.1371/journal.pone.0151048 |
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author | Beier, Paul Albuquerque, Fábio |
author_facet | Beier, Paul Albuquerque, Fábio |
author_sort | Beier, Paul |
collection | PubMed |
description | Species turnover or β diversity is a conceptually attractive surrogate for conservation planning. However, there has been only 1 attempt to determine how well sites selected to maximize β diversity represent species, and that test was done at a scale too coarse (2,500 km(2) sites) to inform most conservation decisions. We used 8 plant datasets, 3 bird datasets, and 1 mammal dataset to evaluate whether sites selected to span β diversity will efficiently represent species at finer scale (sites sizes < 1 ha to 625 km(2)). We used ordinations to characterize dissimilarity in species assemblages (β diversity) among plots (inventory data) or among grid cells (atlas data). We then selected sites to maximize β diversity and used the Species Accumulation Index, SAI, to evaluate how efficiently the surrogate (selecting sites for maximum β diversity) represented species in the same taxon. Across all 12 datasets, sites selected for maximum β diversity represented species with a median efficiency of 24% (i.e., the surrogate was 24% more effective than random selection of sites), and an interquartile range of 4% to 41% efficiency. β diversity was a better surrogate for bird datasets than for plant datasets, and for atlas datasets with 10-km to 14-km grid cells than for atlas datasets with 25-km grid cells. We conclude that β diversity is more than a mere descriptor of how species are distributed on the landscape; in particular β diversity might be useful to maximize the complementarity of a set of sites. Because we tested only within-taxon surrogacy, our results do not prove that β diversity is useful for conservation planning. But our results do justify further investigation to identify the circumstances in which β diversity performs well, and to evaluate it as a cross-taxon surrogate. |
format | Online Article Text |
id | pubmed-4778865 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-47788652016-03-23 Evaluating β Diversity as a Surrogate for Species Representation at Fine Scale Beier, Paul Albuquerque, Fábio PLoS One Research Article Species turnover or β diversity is a conceptually attractive surrogate for conservation planning. However, there has been only 1 attempt to determine how well sites selected to maximize β diversity represent species, and that test was done at a scale too coarse (2,500 km(2) sites) to inform most conservation decisions. We used 8 plant datasets, 3 bird datasets, and 1 mammal dataset to evaluate whether sites selected to span β diversity will efficiently represent species at finer scale (sites sizes < 1 ha to 625 km(2)). We used ordinations to characterize dissimilarity in species assemblages (β diversity) among plots (inventory data) or among grid cells (atlas data). We then selected sites to maximize β diversity and used the Species Accumulation Index, SAI, to evaluate how efficiently the surrogate (selecting sites for maximum β diversity) represented species in the same taxon. Across all 12 datasets, sites selected for maximum β diversity represented species with a median efficiency of 24% (i.e., the surrogate was 24% more effective than random selection of sites), and an interquartile range of 4% to 41% efficiency. β diversity was a better surrogate for bird datasets than for plant datasets, and for atlas datasets with 10-km to 14-km grid cells than for atlas datasets with 25-km grid cells. We conclude that β diversity is more than a mere descriptor of how species are distributed on the landscape; in particular β diversity might be useful to maximize the complementarity of a set of sites. Because we tested only within-taxon surrogacy, our results do not prove that β diversity is useful for conservation planning. But our results do justify further investigation to identify the circumstances in which β diversity performs well, and to evaluate it as a cross-taxon surrogate. Public Library of Science 2016-03-04 /pmc/articles/PMC4778865/ /pubmed/26943170 http://dx.doi.org/10.1371/journal.pone.0151048 Text en © 2016 Beier, Albuquerque 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 use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Beier, Paul Albuquerque, Fábio Evaluating β Diversity as a Surrogate for Species Representation at Fine Scale |
title | Evaluating β Diversity as a Surrogate for Species Representation at Fine Scale |
title_full | Evaluating β Diversity as a Surrogate for Species Representation at Fine Scale |
title_fullStr | Evaluating β Diversity as a Surrogate for Species Representation at Fine Scale |
title_full_unstemmed | Evaluating β Diversity as a Surrogate for Species Representation at Fine Scale |
title_short | Evaluating β Diversity as a Surrogate for Species Representation at Fine Scale |
title_sort | evaluating β diversity as a surrogate for species representation at fine scale |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4778865/ https://www.ncbi.nlm.nih.gov/pubmed/26943170 http://dx.doi.org/10.1371/journal.pone.0151048 |
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