首页> 外文期刊>Methods in Ecology and Evolution >An environmental DNA-based method for monitoring spawning activity: a case study, using the endangered Macquarie perch (Macquaria australasica)
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An environmental DNA-based method for monitoring spawning activity: a case study, using the endangered Macquarie perch (Macquaria australasica)

机译:一种用于监测产卵活动的基于环境DNA的方法:用濒危麦格威鲈鱼(Macquaria Asserralasica)为例

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摘要

Determining the timing and location of reproductive events is critical for efficient management of species. However, methods currently used for aquatic species are costly, time intensive, biased and often require destructive or injurious sampling. Hence, developing a non-invasive sampling method to accurately determine the timing and location of reproduction for aquatic species would be extremely valuable. We conducted an experimental and field study to determine the influence of spawning, and the mass release of spermatozoa in particular, on environmental DNA (eDNA) concentrations. Using a quantitative PCR approach we monitored changes in nuclear and mitochondrial eDNA concentrations over time. The data from the experimental study and the field survey supported our hypothesis that spawning events are characterized by higher concentrations of nuclear relative to mitochondrial eDNA. Outside of the reproductive period, we find that nuclear and mitochondrial DNA fragments are equally abundant in environmental water samples. We have shown that changes in the relative abundance of nuclear and mitochondrial eDNA can be used to monitor spawning activity of the endangered Macquarie perch. Our method is likely to be transferrable to other aquatic species and can be particularly useful to increase our understanding of the spawning biology of cryptic, rare or threatened species as well as design and evaluate environmental management actions and determine species establishment.
机译:确定生殖事件的定时和位置对于有效的物种管理至关重要。然而,目前用于水生物种的方法是昂贵的,时间密集,偏见,往往需要破坏性或有害的抽样。因此,开发非侵入式采样方法以准确地确定用于水生物种的繁殖的定时和位置是非常有价值的。我们进行了实验和现场研究以确定产卵的影响,特别是精子释放,特别是对环境DNA(EDNA)浓度。使用定量PCR方法,我们随着时间的推移监测核和线粒体EDNA浓度的变化。来自实验研究和现场调查的数据支持我们的假设,即产卵事件的特征是较高浓度的核相对于线粒体EDNA。在生殖期间,我们发现核和线粒体DNA片段在环境水样中同样丰富。我们已经表明,核和线粒体eDNA相对丰富的变化可用于监测濒危麦格理栖息地的产卵活性。我们的方法可能会转移到其他水生物种中,可以特别有用,可以提高我们对神秘,稀有或受威胁物种的产卵生物以及设计和评估环境管理行动并确定物种的理解。

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