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On the selection of thresholds for predicting species occurrence with presence‐only data
Presence‐only data present challenges for selecting thresholds to transform species distribution modeling results into binary outputs. In this article, we compare two recently published threshold selection methods (maxSSS and maxF (pb)) and examine the effectiveness of the threshold‐based prevalence...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4716501/ https://www.ncbi.nlm.nih.gov/pubmed/26811797 http://dx.doi.org/10.1002/ece3.1878 |
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author | Liu, Canran Newell, Graeme White, Matt |
author_facet | Liu, Canran Newell, Graeme White, Matt |
author_sort | Liu, Canran |
collection | PubMed |
description | Presence‐only data present challenges for selecting thresholds to transform species distribution modeling results into binary outputs. In this article, we compare two recently published threshold selection methods (maxSSS and maxF (pb)) and examine the effectiveness of the threshold‐based prevalence estimation approach. Six virtual species with varying prevalence were simulated within a real landscape in southeastern Australia. Presence‐only models were built with DOMAIN, generalized linear model, Maxent, and Random Forest. Thresholds were selected with two methods maxSSS and maxF (pb) with four presence‐only datasets with different ratios of the number of known presences to the number of random points (KP–RP (ratio)). Sensitivity, specificity, true skill statistic, and F measure were used to evaluate the performance of the results. Species prevalence was estimated as the ratio of the number of predicted presences to the total number of points in the evaluation dataset. Thresholds selected with maxF (pb) varied as the KP–RP (ratio) of the threshold selection datasets changed. Datasets with the KP–RP (ratio) around 1 generally produced better results than scores distant from 1. Results produced by We conclude that maxF(pb) had specificity too low for very common species using Random Forest and Maxent models. In contrast, maxSSS produced consistent results whichever dataset was used. The estimation of prevalence was almost always biased, and the bias was very large for DOMAIN and Random Forest predictions. We conclude that maxF (pb) is affected by the KP–RP (ratio) of the threshold selection datasets, but maxSSS is almost unaffected by this ratio. Unbiased estimations of prevalence are difficult to be determined using the threshold‐based approach. |
format | Online Article Text |
id | pubmed-4716501 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-47165012016-01-25 On the selection of thresholds for predicting species occurrence with presence‐only data Liu, Canran Newell, Graeme White, Matt Ecol Evol Original Research Presence‐only data present challenges for selecting thresholds to transform species distribution modeling results into binary outputs. In this article, we compare two recently published threshold selection methods (maxSSS and maxF (pb)) and examine the effectiveness of the threshold‐based prevalence estimation approach. Six virtual species with varying prevalence were simulated within a real landscape in southeastern Australia. Presence‐only models were built with DOMAIN, generalized linear model, Maxent, and Random Forest. Thresholds were selected with two methods maxSSS and maxF (pb) with four presence‐only datasets with different ratios of the number of known presences to the number of random points (KP–RP (ratio)). Sensitivity, specificity, true skill statistic, and F measure were used to evaluate the performance of the results. Species prevalence was estimated as the ratio of the number of predicted presences to the total number of points in the evaluation dataset. Thresholds selected with maxF (pb) varied as the KP–RP (ratio) of the threshold selection datasets changed. Datasets with the KP–RP (ratio) around 1 generally produced better results than scores distant from 1. Results produced by We conclude that maxF(pb) had specificity too low for very common species using Random Forest and Maxent models. In contrast, maxSSS produced consistent results whichever dataset was used. The estimation of prevalence was almost always biased, and the bias was very large for DOMAIN and Random Forest predictions. We conclude that maxF (pb) is affected by the KP–RP (ratio) of the threshold selection datasets, but maxSSS is almost unaffected by this ratio. Unbiased estimations of prevalence are difficult to be determined using the threshold‐based approach. John Wiley and Sons Inc. 2015-12-29 /pmc/articles/PMC4716501/ /pubmed/26811797 http://dx.doi.org/10.1002/ece3.1878 Text en © 2015 The Authors. Ecology and Evolution published by John Wiley & Sons Ltd. This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Research Liu, Canran Newell, Graeme White, Matt On the selection of thresholds for predicting species occurrence with presence‐only data |
title | On the selection of thresholds for predicting species occurrence with presence‐only data |
title_full | On the selection of thresholds for predicting species occurrence with presence‐only data |
title_fullStr | On the selection of thresholds for predicting species occurrence with presence‐only data |
title_full_unstemmed | On the selection of thresholds for predicting species occurrence with presence‐only data |
title_short | On the selection of thresholds for predicting species occurrence with presence‐only data |
title_sort | on the selection of thresholds for predicting species occurrence with presence‐only data |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4716501/ https://www.ncbi.nlm.nih.gov/pubmed/26811797 http://dx.doi.org/10.1002/ece3.1878 |
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