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Effectiveness assessment of using riverine water eDNA to simultaneously monitor the riverine and riparian biodiversity information

文献类型: 外文期刊

作者: Yang, Haile 1 ; Du, Hao 1 ; Qi, Hongfang 2 ; Yu, Luxian 2 ; Hou, Xindong 3 ; Zhang, Hui 1 ; Li, Junyi 1 ; Wu, Jinming 1 ; Wang, Chengyou 1 ; Zhou, Qiong 1 ; Wei, Qiwei 1 ;

作者机构: 1.Chinese Acad Fishery Sci, Yangtze River Fisheries Res Inst, Minist Agr & Rural Affairs China, Key Lab Freshwater Biodivers Conservat, Wuhan 430223, Peoples R China

2.Rescue & Rehabil Ctr Naked Carps Qinghai Lake, Qinghai Key Lab Qinghai Lake Naked Carps Breeding, Xining 810016, Peoples R China

3.China Univ Geosci, State Key Lab Biogeol & Environm Geol, Wuhan 430074, Peoples R China

期刊名称:SCIENTIFIC REPORTS ( 影响因子:4.996; 五年影响因子:5.516 )

ISSN: 2045-2322

年卷期: 2021 年 11 卷 1 期

页码:

收录情况: SCI

摘要: Both aquatic and terrestrial biodiversity information can be detected in riverine water environmental DNA (eDNA). However, the effectiveness of using riverine water eDNA to simultaneously monitor the riverine and terrestrial biodiversity information remains unidentified. Here, we proposed that the monitoring effectiveness could be approximated by the transportation effectiveness of land-to-river and upstream-to-downstream biodiversity information flows and described by three new indicators. Subsequently, we conducted a case study in a watershed on the Qinghai-Tibet Plateau. The results demonstrated that there was higher monitoring effectiveness on summer or autumn rainy days than in other seasons and weather conditions. The monitoring of the bacterial biodiversity information was more efficient than the monitoring of the eukaryotic biodiversity information. On summer rainy days, 43-76% of species information in riparian sites could be detected in adjacent riverine water eDNA samples, 92-99% of species information in riverine sites could be detected in a 1-km downstream eDNA sample, and half of dead bioinformation (the bioinformation labeling the biological material that lacked life activity and fertility) could be monitored 4-6 km downstream for eukaryotes and 13-19 km downstream for bacteria. The current study provided reference method and data for future monitoring projects design and for future monitoring results evaluation.

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