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Investigating the distribution of the Yangtze finless porpoise in the Yangtze River using environmental DNA
Determining the distribution of the Yangtze finless porpoise (Neophocaena asiaeorientalis asiaeorientalis, YFP) in the Yangtze River has to date relied on traditional visual and counting methods, but such field surveys are time-consuming and expensive. Analyses using environmental DNA (eDNA) to inve...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6688821/ https://www.ncbi.nlm.nih.gov/pubmed/31398225 http://dx.doi.org/10.1371/journal.pone.0221120 |
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author | Tang, Yongkai Wu, Yunsheng Liu, Kai Li, Jianlin Li, Hongxia Wang, Qin Yu, Juhua Xu, Pao |
author_facet | Tang, Yongkai Wu, Yunsheng Liu, Kai Li, Jianlin Li, Hongxia Wang, Qin Yu, Juhua Xu, Pao |
author_sort | Tang, Yongkai |
collection | PubMed |
description | Determining the distribution of the Yangtze finless porpoise (Neophocaena asiaeorientalis asiaeorientalis, YFP) in the Yangtze River has to date relied on traditional visual and counting methods, but such field surveys are time-consuming and expensive. Analyses using environmental DNA (eDNA) to investigate the presence and range of endangered aquatic species have proven to be more economical and effective detection methods, and are a non-invasive approach to sampling. A challenge of relying on eDNA for YFP monitoring is that the Yangtze River is characterized by high turbidity and a strong current. Here, we used an eDNA-based approach to estimate the presence of YFP at 18 sites in the Yangtze River in August 2017 and at an additional 11 sites in January 2018. At each sampling site, we filtered six 1 L water samples with 5 µm pore size filter paper and quantified the amount of YFP eDNA in each water sample using quantitative real-time polymerase chain reaction (qPCR). In addition, YFP eDNA was successfully detected in locations where we visually observed YFP, as well as in locations where YFP were not observed directly. We found that our eDNA-based method had higher detection rates than traditional field survey methods. Although YFP was visually observed in the Yangtze River in winter, water samples collected during the summer contained significantly higher YFP eDNA than winter water samples. Our results demonstrate the potential effectiveness of eDNA detection methods in determining the distribution of YFP in the Yangtze River. |
format | Online Article Text |
id | pubmed-6688821 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-66888212019-08-15 Investigating the distribution of the Yangtze finless porpoise in the Yangtze River using environmental DNA Tang, Yongkai Wu, Yunsheng Liu, Kai Li, Jianlin Li, Hongxia Wang, Qin Yu, Juhua Xu, Pao PLoS One Research Article Determining the distribution of the Yangtze finless porpoise (Neophocaena asiaeorientalis asiaeorientalis, YFP) in the Yangtze River has to date relied on traditional visual and counting methods, but such field surveys are time-consuming and expensive. Analyses using environmental DNA (eDNA) to investigate the presence and range of endangered aquatic species have proven to be more economical and effective detection methods, and are a non-invasive approach to sampling. A challenge of relying on eDNA for YFP monitoring is that the Yangtze River is characterized by high turbidity and a strong current. Here, we used an eDNA-based approach to estimate the presence of YFP at 18 sites in the Yangtze River in August 2017 and at an additional 11 sites in January 2018. At each sampling site, we filtered six 1 L water samples with 5 µm pore size filter paper and quantified the amount of YFP eDNA in each water sample using quantitative real-time polymerase chain reaction (qPCR). In addition, YFP eDNA was successfully detected in locations where we visually observed YFP, as well as in locations where YFP were not observed directly. We found that our eDNA-based method had higher detection rates than traditional field survey methods. Although YFP was visually observed in the Yangtze River in winter, water samples collected during the summer contained significantly higher YFP eDNA than winter water samples. Our results demonstrate the potential effectiveness of eDNA detection methods in determining the distribution of YFP in the Yangtze River. Public Library of Science 2019-08-09 /pmc/articles/PMC6688821/ /pubmed/31398225 http://dx.doi.org/10.1371/journal.pone.0221120 Text en © 2019 Tang et al 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 Tang, Yongkai Wu, Yunsheng Liu, Kai Li, Jianlin Li, Hongxia Wang, Qin Yu, Juhua Xu, Pao Investigating the distribution of the Yangtze finless porpoise in the Yangtze River using environmental DNA |
title | Investigating the distribution of the Yangtze finless porpoise in the Yangtze River using environmental DNA |
title_full | Investigating the distribution of the Yangtze finless porpoise in the Yangtze River using environmental DNA |
title_fullStr | Investigating the distribution of the Yangtze finless porpoise in the Yangtze River using environmental DNA |
title_full_unstemmed | Investigating the distribution of the Yangtze finless porpoise in the Yangtze River using environmental DNA |
title_short | Investigating the distribution of the Yangtze finless porpoise in the Yangtze River using environmental DNA |
title_sort | investigating the distribution of the yangtze finless porpoise in the yangtze river using environmental dna |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6688821/ https://www.ncbi.nlm.nih.gov/pubmed/31398225 http://dx.doi.org/10.1371/journal.pone.0221120 |
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