底拖网和多标记 eDNA 元条码调查揭示了高度多样化的脊椎动物和甲壳动物群落:城市化亚热带河口案例研究

Q1 Agricultural and Biological Sciences
Jack Chi-Ho Ip, Hai-Xin Loke, Sam King Fung Yiu, Meihong Zhao, Yixuan Li, Yitao Lin, Chun-Ming How, Jiezhang Mo, Meng Yan, Jinping Cheng, Vincent Chi-Sing Lai, Leo Lai Chan, Kenneth Mei Yee Leung, Jian-Wen Qiu
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引用次数: 0

摘要

河口栖息地是许多水生物种的重要觅食地和育苗地,并为渔业提供支持。然而,使用传统的拖网方法监测这些复杂的生态系统破坏性大、成本高且劳动密集。本研究比较了拖网和多标记环境 DNA(eDNA)代谢编码方法,以监测香港亚热带河口环境中的海洋脊椎动物和甲壳动物群落。我们使用鱼类和哺乳动物(MiFish-U、12S-V5 和 Berry-Fish)以及十足目甲壳动物(MiDeca)的特异引物集,分析了 16 个底拖网样本和 32 个两升水样的 eDNA。我们发现,与拖网法相比,eDNA 法检测到的中上层鱼类(237 种)和底栖鱼类(106 种)以及韧皮动物(6 种)更多。在检测受威胁脊椎动物方面,eDNA 方法也比拖网法更有效(16 对 4),包括印度太平洋江豚和极度濒危的大黄鱼。在检测到的鱼类物种中,两种方法都检测到 70 个物种,仅拖网检测到 32 个物种,仅 eDNA 方法检测到 142 个物种。在甲壳类动物方面,eDNA 方法检测到的十足类(61 种对 77 种)和口足类(5 种对 8 种)略少于拖网调查。不过,eDNA 方法可以通过开发合适的十足目动物特异引物和扩大本地参考数据库得到改进。此外,对 eDNA 数据的多元分析显示,鱼类和甲壳类动物群落的空间模式可能与沉积物负荷、氧气和营养水平有关。此外,eDNA 读数与拖网渔获量之间存在正相关,但相关系数较低。我们的结论是,eDNA 代谢编码可对河口生态系统中的物种、组成进行高分辨率检测,并揭示群落与环境之间的关系。总之,将非破坏性的 eDNA 方法与传统的拖网方法相结合,可以为可持续渔业管理和保护提供更多信息。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Bottom Trawling and Multi-Marker eDNA Metabarcoding Surveys Reveal Highly Diverse Vertebrate and Crustacean Communities: A Case Study in an Urbanized Subtropical Estuary

Bottom Trawling and Multi-Marker eDNA Metabarcoding Surveys Reveal Highly Diverse Vertebrate and Crustacean Communities: A Case Study in an Urbanized Subtropical Estuary

Estuarine habitats serve as critical feeding and nursery grounds for many aquatic species and support fisheries. However, monitoring these complex ecosystems using conventional trawling methods is destructive, costly, and labor-intensive. This study compared trawling and a multi-marker environmental DNA (eDNA) metabarcoding approach to monitor marine vertebrate and crustacean communities in an estuarine environment in subtropical Hong Kong. We analyzed 16 bottom trawl samples and the eDNA from 32 two-liter water samples using primer sets specific to fishes and mammals (MiFish-U, 12S-V5, and Berry-Fish) and decapod crustaceans (MiDeca). We found that the eDNA approach detected more pelagic and demersal fishes (237 vs. 106 in trawling) and elasmobranchs (6 vs. 3) than trawling. The eDNA approach was also more effective than trawling in detecting threatened vertebrates (16 vs. 4), including the Indo-Pacific Finless Porpoise and the critically endangered Large Yellow Croaker. Among the detected fish at species level, 70 species were detected by both approaches, 32 species were detected by trawling only, and 142 species were detected by the eDNA approach only. Regarding crustaceans, the eDNA approach detected slightly fewer decapods (61 vs. 77) and stomatopods (5 vs. 8) than trawl surveys. However, the eDNA approach could be enhanced through the development of suitable decapod-specific primers and the expansion of the local reference database. In addition, multivariate analyses of the eDNA data revealed spatial patterns of fish and crustacean assemblages that might be associated with sediment loading, oxygen, and nutrient levels. Furthermore, there was a positive correlation between eDNA read counts and trawl catch, but their correlation coefficient was low. We conclude that eDNA metabarcoding can provide high-resolution detection of species, composition, and unravel community–environment relationships in estuarine ecosystems. Overall, integrating the non-destructive eDNA approach can complement the conventional trawling method for better-informed sustainable fishery management and conservation.

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来源期刊
Environmental DNA
Environmental DNA Agricultural and Biological Sciences-Ecology, Evolution, Behavior and Systematics
CiteScore
11.00
自引率
0.00%
发文量
99
审稿时长
16 weeks
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