kicknet采样、eDNA代谢编码和预测建模的三元组合,用于评估河流中mayflies、stoneflies和caddisflies的丰富度

F. Keck, Samuel Hürlemann, Nadine Locher, C. Stamm, Kristy Deiner, F. Altermatt
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引用次数: 4

摘要

监测生物多样性对于了解人类活动的影响和有效管理生态系统至关重要。因此,可以通过直接收集目标生物,通过间接证据证明其存在(如迹象、环境DNA、相机陷阱等),或通过从物种分布和物种丰富度模型推断来评估生物多样性。然而,生物多样性评估中使用的方法的差异可能会带来个人挑战,并阻碍跨研究的可比性。在快速发展的技术背景下,我们比较了三种不同的方法,以更好地了解水生大型无脊椎动物多样性的评估。具体而言,我们将通过eDNA代谢编码和传统的原位踢球网采样获得的三个目水生大型无脊椎动物(五月蝇、石蝇和石蛾,以下简称EPT)的群落组成和物种丰富度与基于集水区水平的物种丰富度模型预测进行了比较。我们使用了来自瑞士24个地点的kicknet数据,并将分类列表与使用两个不同引物组扩增的eDNA获得的分类列表进行了比较。将这些方法检测到的丰富度与统计物种丰富度模型(即使用景观水平特征来估计EPT多样性的广义线性模型)进行的独立预测进行了比较。尽管eDNA能够始终如一地检测传统采样发现的一些EPT物种,但我们发现kicknet和eDNA方法之间的群落组成存在重要差异,特别是在局部范围内。我们发现EPT特异性引物组fwhF2/EPTDr2n,与更通用的引物组mlCOIntF/HCO2198相比,检测到更多的靶向EPT物种。此外,我们发现,通过任一引物集的eDNA测量的物种丰富度与通过kicknet采样测量的丰富度相关性较差(Pearson相关性=0.27),并且通过eDNA和kicknet估计的丰富度与物种丰富度模型的预测相关性较差(分别为Pearson相关=0.30和0.44)。传统的kicknet采样和该模型的eDNA之间的弱关系表明,在扩大物种丰富度估计方面存在固有的局限性,并且该模型满足现实世界期望的能力可能有限。也有可能重复次数不足以检测不明确的相关性。未来的挑战包括分别提高每种方法的准确性和敏感性,同时承认其各自的局限性,以最好地满足利益相关者的需求,并解决我们面临的生物多样性危机。
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A triad of kicknet sampling, eDNA metabarcoding, and predictive modeling to assess richness of mayflies, stoneflies and caddisflies in rivers
Monitoring biodiversity is essential to understand the impacts of human activities and for effective management of ecosystems. Thereby, biodiversity can be assessed through direct collection of targeted organisms, through indirect evidence of their presence (e.g. signs, environmental DNA, camera trap, etc.), or through extrapolations from species distribution and species richness models. Differences in approaches used in biodiversity assessment, however, may come with individual challenges and hinder cross-study comparability. In the context of rapidly developing techniques, we compared three different approaches in order to better understand assessments of aquatic macroinvertebrate diversity. Specifically, we compared the community composition and species richness of three orders of aquatic macroinvertebrates (mayflies, stoneflies, and caddisflies, hereafter EPT) obtained via eDNA metabarcoding and via traditional in situ kicknet sampling to catchment-level based predictions of a species richness model. We used kicknet data from 24 sites in Switzerland and compared taxonomic lists to those obtained using eDNA amplified with two different primer sets. Richness detected by these methods was compared to the independent predictions made by a statistical species richness model, that is, a generalized linear model using landscape-level features to estimate EPT diversity. Despite the ability of eDNA to consistently detect some EPT species found by traditional sampling, we found important discrepancies in community composition between the kicknet and eDNA approaches, particularly at a local scale. We found the EPT-specific primer set fwhF2/EPTDr2n, detected a greater number of targeted EPT species compared to the more general primer set mlCOIintF/HCO2198. Moreover, we found that the species richness measured by eDNA from either primer set was poorly correlated to the richness measured by kicknet sampling (Pearson correlation = 0.27) and that the richness estimated by eDNA and kicknet were poorly correlated with the prediction of the species richness model (Pearson correlation = 0.30 and 0.44, respectively). The weak relationships between the traditional kicknet sampling and eDNA with this model indicates inherent limitations in upscaling species richness estimates, and possibly a limited ability of the model to meet real world expectations. It is also possible that the number of replicates was not sufficient to detect ambiguous correlations. Future challenges include improving the accuracy and sensitivity of each approach individually, yet also acknowledging their respective limitations, in order to best meet stakeholder demands and address the biodiversity crisis we are facing.
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Metabarcoding and Metagenomics
Metabarcoding and Metagenomics Agricultural and Biological Sciences-Animal Science and Zoology
CiteScore
5.40
自引率
0.00%
发文量
25
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