Darling John A, Jerde Christopher L, Sepulveda Adam J
Center for Environmental Measurement & Modeling, United States Environmental Protection Agency, Research Triangle Park, NC, USA.
Marine Science Institute, University of California, Santa Barbara, CA, USA.
Environ DNA. 2020 Nov 25;3(5):879-883. doi: 10.1002/edn3.194.
Misunderstandings regarding the term "false positive" present a significant hurdle to broad adoption of eDNA monitoring methods. Here, we identify three challenges to clear communication of false-positive error between scientists, managers, and the public. The first arises from a failure to distinguish between false-positive eDNA detection at the sample level and false-positive inference of taxa presence at the site level. The second is based on the large proportion of false positives that may occur when true-positive detections are likely to be rare, even when rates of contamination or other error are low. And the third misunderstanding occurs when conventional species detection approaches, often based on direct capture, are used to confirm eDNA approaches without acknowledging or quantifying the conventional approach's detection probability. The solutions to these issues include careful and consistent communication of error definitions, managing expectations of error rates, and providing a balanced discussion not only of alternative sources of species DNA, but also of the detection limitations of conventional methods. We argue that the benefit of addressing these misunderstandings will be increased confidence in the utility of eDNA methods and, ultimately, improved resource management using eDNA approaches. The term false positive is often misused in eDNA research and natural resource management. There are issues of scale of inference, the base rate fallacy, and confirmation errors using conventional methods of detection. We offer a perspective to guide discussions of errors in species detection.
对“假阳性”一词的误解成为广泛采用环境DNA监测方法的重大障碍。在此,我们确定了在科学家、管理人员和公众之间清晰传达假阳性错误的三个挑战。第一个挑战源于未能区分样本层面的环境DNA假阳性检测和位点层面分类单元存在的假阳性推断。第二个挑战基于这样一个事实,即即使污染率或其他错误率很低,但在真阳性检测可能很少的情况下,仍可能出现大量假阳性。第三个误解发生在使用通常基于直接捕获的传统物种检测方法来确认环境DNA方法时,却未承认或量化传统方法的检测概率。解决这些问题的方法包括谨慎且一致地传达错误定义、管理对错误率的预期,以及不仅对物种DNA的其他来源,而且对传统方法的检测局限性进行平衡的讨论。我们认为,解决这些误解的好处将是增强对环境DNA方法效用的信心,并最终改善使用环境DNA方法的资源管理。在环境DNA研究和自然资源管理中,“假阳性”一词经常被误用。存在推断规模、基础比率谬误以及使用传统检测方法时的确认错误等问题。我们提供了一个视角来指导有关物种检测中错误的讨论。