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从环境DNA浓度估算鱼类丰度和生物量:捕获方法与环境条件的变异性

Estimating fish abundance and biomass from eDNA concentrations: variability among capture methods and environmental conditions.

作者信息

Lacoursière-Roussel Anaïs, Rosabal Maikel, Bernatchez Louis

机构信息

Institut de Biologie Intégrative et des Systèmes (IBIS), Pavillon Charles Eugène Marchand, Université Laval, Québec, QC, G1V 0A6, Canada.

Institut National de la Recherche Scientifique (INRS), Centre Eau Terre Environnement (INRS-ETE), 490 de la Couronne, Québec, QC, G1K 9A9, Canada.

出版信息

Mol Ecol Resour. 2016 Nov;16(6):1401-1414. doi: 10.1111/1755-0998.12522. Epub 2016 Mar 28.

Abstract

Environmental DNA (eDNA) promises to ease noninvasive quantification of fish biomass or abundance, but its integration within conservation and fisheries management is currently limited by a lack of understanding of the influence of eDNA collection method and environmental conditions on eDNA concentrations in water samples. Water temperature is known to influence the metabolism of fish and consequently could strongly affect eDNA release rate. As water temperature varies in temperate regions (both seasonally and geographically), the unknown effect of water temperature on eDNA concentrations poses practical limitations on quantifying fish populations using eDNA from water samples. This study aimed to clarify how water temperature and the eDNA capture method alter the relationships between eDNA concentration and fish abundance/biomass. Water samples (1 L) were collected from 30 aquaria including triplicate of 0, 5, 10, 15 and 20 Brook Charr specimens at two different temperatures (7 °C and 14 °C). Water samples were filtered with five different types of filters. The eDNA concentration obtained by quantitative PCR (qPCR) varied significantly with fish abundance and biomass and types of filters (mixed-design ANOVA, P < 0.001). Results also show that fish released more eDNA in warm water than in cold water and that eDNA concentration better reflects fish abundance/biomass at high temperature. From a technical standpoint, higher levels of eDNA were captured with glass fibre (GF) filters than with mixed cellulose ester (MCE) filters and support the importance of adequate filters to quantify fish abundance based on the eDNA method. This study supports the importance of including water temperature in fish abundance/biomass prediction models based on eDNA.

摘要

环境DNA(eDNA)有望简化鱼类生物量或丰度的非侵入性定量分析,但目前其在保护和渔业管理中的应用受到限制,因为人们对eDNA收集方法和环境条件对水样中eDNA浓度的影响缺乏了解。已知水温会影响鱼类的新陈代谢,因此可能强烈影响eDNA的释放速率。由于温带地区的水温会发生变化(包括季节性和地理性变化),水温对eDNA浓度的未知影响给利用水样中的eDNA定量鱼类种群带来了实际限制。本研究旨在阐明水温和eDNA捕获方法如何改变eDNA浓度与鱼类丰度/生物量之间的关系。从30个水族箱中采集了水样(1升),其中包括在两种不同温度(7℃和14℃)下分别有0、5、10、15和20条溪红点鲑样本的三份重复样本。水样用五种不同类型的滤膜进行过滤。通过定量聚合酶链反应(qPCR)获得的eDNA浓度随鱼类丰度、生物量以及滤膜类型的不同而有显著差异(混合设计方差分析,P<0.001)。结果还表明,鱼类在温水中释放的eDNA比在冷水中更多,并且eDNA浓度在高温下能更好地反映鱼类丰度/生物量。从技术角度来看,玻璃纤维(GF)滤膜捕获的eDNA水平高于混合纤维素酯(MCE)滤膜,这也支持了使用合适滤膜对于基于eDNA方法定量鱼类丰度的重要性。本研究支持了在基于eDNA的鱼类丰度/生物量预测模型中纳入水温的重要性。

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