Drastic decline in spawning activity of Chinese sturgeon Acipenser sinensis Gray 1835 in the remaining spawning ground of the Yangtze River since the construction of hydrodams

2015 ◽  
Vol 31 (5) ◽  
pp. 839-842 ◽  
Author(s):  
J. M. Wu ◽  
C. Y. Wang ◽  
H. Zhang ◽  
H. Du ◽  
Z. G. Liu ◽  
...  
Keyword(s):  
Yangtze River ◽  
The Yangtze River ◽  
Spawning Ground ◽  
Chinese Sturgeon ◽  
Spawning Activity ◽  
Acipenser Sinensis

scholarly journals Using environmental DNA methods to improve detectability in an endangered sturgeon (Acipenser sinensis) monitoring program

2021 ◽  
Vol 21 (1) ◽  
Author(s):  
Dan Yu ◽  
Zhongyuan Shen ◽  
Tao Chang ◽  
Sha Li ◽  
Huanzhang Liu
Keyword(s):  
Yangtze River ◽  
Limit Of Detection ◽  
Monitoring Program ◽  
Environmental Dna ◽  
Aquatic Species ◽  
The Yangtze River ◽  
Spawning Ground ◽  
Chinese Sturgeon ◽  
Temporal And Spatial Distribution ◽  
Acipenser Sinensis

Abstract Background To determine the presence and abundance of an aquatic species in large waterbodies, especially when populations are at low densities, is highly challenging for conservation biologists. Environmental DNA (eDNA) has the potential to offer a noninvasive and cost-effective method to complement traditional population monitoring, however, eDNA has not been extensively applied to study large migratory species. Chinese sturgeon (Acipenser sinensis), is the largest anadromous migratory fish in the Yangtze River, China, and in recent years its population has dramatically declined and spawning has failed, bringing this species to the brink of extinction. In this study, we aim to test the detectability of eDNA methods to determine the presence and relative abundance of reproductive stock of the species and whether eDNA can be used as a tool to reflect behavioral patterns. Chinese sturgeon eDNA was collected from four sites along the spawning ground across an eight month period, to investigate the temporal and spatial distribution using droplet digital PCR (ddPCR). Results We designed a pair of specific primers for Chinese sturgeon and demonstrated the high sensitivity of ddPCR to detect and quantify the Chinese sturgeon eDNA concentration with the limit of detection 0.17 copies/μl, with Chinese sturgeon eDNA been intermittently detected at all sampling sites. There was a consistent temporal pattern among four of the sampling sites that could reflect the movement characteristics of the Chinese sturgeon in the spawning ground, but without a spatial pattern. The eDNA concentration declined by approximately 2–3 × between December 2018 and December 2019. Conclusions The results prove the efficacy of eDNA for monitoring reproductive stock of the Chinese sturgeon and the e decreased eDNA concentration reflect that Chinese sturgeon may survive with an extremely small number of reproductive stock in the Yangtze River. Accordingly, we suggest future conservation measures should focus on both habitat restoration and matured fish restocking to ensure successful spawning. Overall, this study provides encouraging support for the application of eDNA methods to monitor endangered aquatic species.

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