环境DNA检测到一种短暂洄游鱼类的产卵栖息地(溯河彩虹鱼:Osmerus mordax)。

Vaughn Holmes, Jacob Aman, Geneva York, Michael T Kinnison
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引用次数: 3

摘要

背景:近几十年来,在缅因州,溯河虹鱼(Osmerus mordax)的数量大幅减少,剩余产卵种群的状况鲜为人知,在缅因州,这些鱼具有重要的生态、文化和商业意义。确定溯河鱼群的残余范围比确定许多正在减少的鱼类种类要困难得多,因为成鱼只在春季径流期间夜间在沿海小溪中产卵时短暂存在,而传统的评估可能不可靠,甚至危险。我们假设eDNA可能有助于改善调查工作,以确定鲑鱼产卵的栖息地,但这种检测也可能面临成年eDNA迅速从这些小溪流系统中冲洗出来的挑战。我们将白天的eDNA采样与夜间的fyke网相结合,以确定eDNA检测的潜在窗口,然后在四个不同丰度的流中进行eDNA调查。然后采用分层占用模型来估计eDNA遇到概率与采样事件(日期)、事件内样本和样本内qPCR重复的数量有关。结果:eDNA和fyke net联合研究结果表明,eDNA在很长一段时间内都可以检测到,在产卵高峰后大约8-13天达到顶峰,这表明发育中的鲑鱼幼虫可能是eDNA的主要来源。随后,在四种河流的eDNA调查中很容易检测到熔体eDNA,特别是在修复PCR抑制剂之后。分层占用模型证实了我们的调查对大多数站点具有较高的经验检测能力,并且未来的调查采用至少三个采样事件,每个事件三个样本和六个qPCR重复,可以在低丰度系统中提供大于90%的组合检测能力。结论:这些结果表明,相对适度的eDNA取样工作具有很高的能力,可以检测到这种短暂存在的低到中等丰度的物种。因此,与现有的视觉和网法相比,嗅觉eDNA检测可以提供更长的调查窗口,更安全的采样条件,以及在低密度系统中更低的现场工作量,从而改善范围测绘。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Environmental DNA detects Spawning Habitat of an ephemeral migrant fish (Anadromous Rainbow Smelt: Osmerus mordax).

Environmental DNA detects Spawning Habitat of an ephemeral migrant fish (Anadromous Rainbow Smelt: Osmerus mordax).

Environmental DNA detects Spawning Habitat of an ephemeral migrant fish (Anadromous Rainbow Smelt: Osmerus mordax).

Environmental DNA detects Spawning Habitat of an ephemeral migrant fish (Anadromous Rainbow Smelt: Osmerus mordax).

Background: Anadromous rainbow smelt (Osmerus mordax) have experienced a large range reduction in recent decades and the status of remnant spawning populations is poorly known in Maine, where these fish have significant ecological, cultural, and commercial relevance. Defining the remnant range of anadromous smelt is more difficult than for many declining fish species because adults are only ephemerally present while spawning in small coastal streams at night during spring runoff periods when traditional assessments can be unreliable or even hazardous. We hypothesized that eDNA might facilitate improved survey efforts to define smelt spawning habitat, but that detection could also face challenges from adult eDNA quickly flushing out of these small stream systems. We combined daytime eDNA sampling with nighttime fyke netting to ascertain a potential window of eDNA detection before conducting eDNA surveys in four streams of varying abundance. Hierarchical occupancy modeling was in turn employed to estimate eDNA encounter probabilities relative to numbers of sampling events (date), samples within events, and qPCR replicates within samples.

Results: Results from the combined eDNA and fyke net study indicated eDNA was detectable over an extended period, culminating approximately 8-13 days following peak spawning, suggesting developing smelt larvae might be the primary source of eDNA. Subsequently, smelt eDNA was readily detected in eDNA surveys of four streams, particularly following remediation of PCR inhibitors. Hierarchical occupancy modeling confirmed our surveys had high empirical detection for most sites, and that future surveys employing at least three sampling events, three samples per event, and six qPCR replicates can afford greater than 90% combined detection capability in low abundance systems.

Conclusions: These results demonstrate that relatively modest eDNA sampling effort has high capacity to detect this ephemerally present species of concern at low to moderate abundances. As such, smelt eDNA detection could improve range mapping by providing longer survey windows, safer sampling conditions, and lower field effort in low density systems, than afforded by existing visual and netting approaches.

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