Optimizing eDNA Replication for Standardized Application in Lotic Systems in Aotearoa, New Zealand

Q1 Agricultural and Biological Sciences
Josh Smith, Bruno David, Andy Hicks, Shaun Wilkinson, Nicolas Ling, Daniel Fake, Alastair Suren, Amy Gault
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引用次数: 0

Abstract

National standardization of ecological sampling protocols between different agencies in Aotearoa New Zealand has historically been difficult to attain, creating challenges for combining datasets for national scale analyses. The introduction of new methods for biological monitoring, such as environmental DNA (eDNA), presents an opportunity to standardize aquatic sampling protocols prior to widespread adoption. The objective of this study was to optimize eDNA sample replication for the consistent characterization of freshwater fish and macroinvertebrate communities in flowing waters, and ultimately, to inform the development of robust national monitoring standards. A comparison of field replication and extraction methods (pooling of preservation buffer) was also trialed as part of this high replication (n = 16) eDNA study to assess any potential benefits in measuring species richness and reducing processing costs alongside replication optimisation. This involved two ‘syringe’ sampling methods (‘standard’ and ‘boosted’, eight each) conducted across 54 riverine sites throughout the country. No significant difference was found for species richness between the standardized (eight replicates) or boosted (16 replicates composited to eight) eDNA methods for fish and macroinvertebrates. Results indicated that six replicates were needed to consistently detect 89.5% of fish species likely to be present using field-based syringe eDNA sampling and preservation. However, an altitudinal species richness effect was observed for fish. For macroinvertebrates, six replicates were required to identify 86% of taxa identified to the NEMS (National Environmental Monitoring Standards) level used for the Macroinvertebrate Community Index (MCI: usually genera) while eight replicates were required to detect 89% of NEMS taxa. For fish and macroinvertebrate biodiversity, this study suggests that six replicates are a reasonable trade-off between effective community characterization and cost in New Zealand lotic systems.

Abstract Image

优化 eDNA 复制,以便在新西兰奥特亚罗瓦的土地系统中实现标准化应用
在新西兰奥特亚罗瓦,不同机构之间的生态采样规程历来难以实现全国标准化,这给合并数据集进行全国范围的分析带来了挑战。环境 DNA(eDNA)等生物监测新方法的引入,为在广泛采用之前实现水生生物取样规程的标准化提供了机会。本研究的目的是优化 eDNA 样品的复制,以便对流动水域中的淡水鱼类和大型无脊椎动物群落进行一致的特征描述,并最终为制定强有力的国家监测标准提供信息。作为这项高重复率(n = 16)eDNA 研究的一部分,还对现场重复和提取方法(保存缓冲液池)进行了比较试验,以评估在测量物种丰富度和降低处理成本的同时优化重复方面的潜在益处。这包括两种 "注射器 "取样方法("标准 "和 "增强",各八种),在全国 54 个河流地点进行。在鱼类和大型无脊椎动物的物种丰富度方面,标准化(8 个重复)和增强(16 个重复合成为 8 个)eDNA 方法没有发现明显差异。结果表明,采用现场注射器 eDNA 采样和保存法,需要 6 个重复才能持续检测到 89.5% 可能存在的鱼类物种。不过,在鱼类方面观察到了海拔物种丰富度效应。在大型无脊椎动物方面,需要 6 次重复才能鉴定出 86% 的分类群,达到用于大型无脊椎动物群落指数(MCI:通常为属)的 NEMS(国家环境监测标准)水平,而需要 8 次重复才能检测出 89% 的 NEMS 分类群。就鱼类和大型无脊椎动物的生物多样性而言,本研究表明,在新西兰地段系统中,6 次重复是有效群落特征描述与成本之间的合理权衡。
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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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