van Bochove Kees, Bakker Freek T, Beentjes Kevin K, Hemerik Lia, Vos Rutger A, Gravendeel Barbara
Biosystematics Group Wageningen University Wageningen The Netherlands.
Naturalis Biodiversity Center Leiden The Netherlands.
Ecol Evol. 2020 Mar 21;10(8):3647-3654. doi: 10.1002/ece3.6123. eCollection 2020 Apr.
Environmental DNA (eDNA) is used for monitoring the occurrence of freshwater organisms. Various studies show a relation between the amount of eDNA detected and target organism abundance, thus providing a potential proxy for reconstructing population densities. However, environmental factors such as water temperature and microbial activity are known to affect the amount of eDNA present as well. In this study, we use controlled aquarium experiments using L. (Amphipoda) to investigate the relationship between the amount of detectable eDNA through time, pH, and levels of organic material. We found eDNA to degrade faster when organic material was added to the aquarium water, but that pH had no significant effect. We infer that eDNA contained inside cells and mitochondria is extra resilient against degradation, though this may not reflect actual presence of target species. These results indicate that, although estimation of population density might be possible using eDNA, measured eDNA concentration could, in the future, be corrected for local environmental conditions in order to ensure accurate comparisons.
环境DNA(eDNA)被用于监测淡水生物的出现情况。各种研究表明,检测到的eDNA量与目标生物丰度之间存在关联,从而为重建种群密度提供了一个潜在的替代指标。然而,已知水温及微生物活动等环境因素也会影响eDNA的存在量。在本研究中,我们使用以L.(双足节动物)进行的受控水族箱实验,来探究随时间推移可检测到的eDNA量、pH值和有机物质水平之间的关系。我们发现,向水族箱水中添加有机物质时,eDNA降解得更快,但pH值没有显著影响。我们推断,细胞和线粒体内所含的eDNA对降解具有更强的抵抗力,尽管这可能无法反映目标物种的实际存在情况。这些结果表明,尽管使用eDNA估计种群密度或许可行,但未来可能需要针对当地环境条件对测得的eDNA浓度进行校正,以确保准确比较。