scholarly journals Passive eDNA collection enhances aquatic biodiversity analysis

2021 ◽  
Vol 4 (1) ◽  
Author(s):  
Cindy Bessey ◽  
Simon Neil Jarman ◽  
Tiffany Simpson ◽  
Haylea Miller ◽  
Todd Stewart ◽  
...  

AbstractEnvironmental DNA (eDNA) metabarcoding is a sensitive and widely used approach for species detection and biodiversity assessment. The most common eDNA collection method in aquatic systems is actively filtering water through a membrane, which is time consuming and requires specialized equipment. Ecological studies investigating species abundance or distribution often require more samples than can be practically collected with current filtration methods. Here we demonstrate how eDNA can be passively collected in both tropical and temperate marine systems by directly submerging filter membranes (positively charged nylon and non-charged cellulose ester) in the water column. Using a universal fish metabarcoding assay, we show that passive eDNA collection can detect fish as effectively as active eDNA filtration methods in temperate systems and can also provide similar estimates of total fish biodiversity. Furthermore, passive eDNA collection enables greater levels of biological sampling, which increases the range of ecological questions that eDNA metabarcoding can address.

2021 ◽  
Vol 4 (1) ◽  
Author(s):  
Cindy Bessey ◽  
Simon Neil Jarman ◽  
Tiffany Simpson ◽  
Haylea Miller ◽  
Todd Stewart ◽  
...  

A Correction to this paper has been published: https://doi.org/10.1038/s42003-021-01994-6


Author(s):  
Toshiaki Jo ◽  
Hiroki Yamanaka

Environmental DNA (eDNA) analysis is a promising tool for non-disruptive and cost-efficient estimation of species abundance. However, its practical applicability in natural environments is limited because it is unclear whether eDNA concentrations actually represent species abundance in the field. Although the importance of accounting for eDNA dynamics, such as transport and degradation, has been discussed, the influences of eDNA characteristics, including production source and state, and methodology, including collection and quantification strategy and abundance metrics, on the accuracy of eDNA-based abundance estimation were entirely overlooked. We conducted a meta-analysis using 56 previous eDNA literature and investigated the relationships between the accuracy (R2) of eDNA-based abundance estimation and eDNA characteristics and methodology. Our meta-regression analysis found that R2 values were significantly lower for crustaceans than fish, suggesting that less frequent eDNA production owing to their external morphology and physiology may impede accurate estimation of their abundance via eDNA. Moreover, R2 values were positively associated with filter pore size, indicating that selective collection of larger-sized eDNA, which is typically fresher, could improve the estimation accuracy of species abundance. Furthermore, R2 values were significantly lower for natural than laboratory conditions, while there was no difference in the estimation accuracy among natural environments. Our findings shed a new light on the importance of what characteristics of eDNA should be targeted for more accurate estimation of species abundance. Further empirical studies are required to validate our findings and fully elucidate the relationship between eDNA characteristics and eDNA-based abundance estimation.


2021 ◽  
Author(s):  
Shunsuke Matsuoka ◽  
Yoriko Sugiyama ◽  
Mariko Nagano ◽  
Hideyuki Doi

Background: Environmental DNA (eDNA) metabarcoding is a rapidly expanding technique for efficient biodiversity monitoring, especially of animals. Recently, the usefulness of aquatic eDNA in monitoring the diversity of both terrestrial and aquatic fungi has been suggested. In eDNA studies, different experimental factors, such as DNA extraction kits or methods, can affect the subsequent analyses and the results of DNA metabarcoding. However, few methodological studies have been carried out on eDNA of fungi, and little is known about how experimental procedures can affect the results of biodiversity analysis. In this study, we focused on the effect of the DNA extraction method on fungal DNA metabarcoding using freshwater samples obtained from rivers and lakes. Methods: DNA was extracted from freshwater samples using the DNeasy PowerSoil kit, which is mainly used to extract microbial DNA from soil, and the DNeasy Blood & Tissue kit, which is commonly used for eDNA studies on animals. We then compared PCR inhibition and fungal DNA metabarcoding results [i.e., operational taxonomic unit (OTU) number and composition] of the extracted samples. Results: No PCR inhibition was detected in any of the samples, and no significant differences in the number of OTUs and OTU compositions were detected between the samples processed using different kits. These results indicate that both DNA extraction kits may provide similar diversity results for the river and lake samples evaluated in this study. Therefore, it may be possible to evaluate the diversity of fungi using a unified experimental method, even with samples obtained for diversity studies on other taxa such as those of animals.


2021 ◽  
Vol 4 ◽  
Author(s):  
PJ Stephenson

Evidence-based decision-making in conservation and natural resource management is often constrained by lack of robust biodiversity data. Technology offers opportunities for enhanced data collection, with satellite-based remote sensing increasingly complemented by Earth-based sensors such as camera traps, acoustic recording devices and drones. In aquatic as well as terrestrial systems, environmental DNA is increasingly promoted as a tool to monitor species diversity and community composition. But if conservationists and natural resource managers are to know when to use eDNA, they need to understand its relative advantages and disadvantages, and when it can be used with or instead of other tools. In this paper, I expand on two recent publications (Stephenson 2020; Stephenson et al. 2020) to review lessons learned from the application of eDNA, especially metabarcoding, to the monitoring of aquatic biodiversity for conservation and to identify factors affecting its relevance and applicability. Over the past decade there have been many advances in technological solutions for biodiversity monitoring. eDNA and various remote sensing tools offer opportunities to create the enabling conditions for enhanced biodiversity monitoring, and are becoming cheaper and easier to use for scientists, public and private sector resource managers, and citizen scientists. Nonetheless, a number of challenges need to be addressed to, for example, improve the standardisation of tool use and to enhance capacity for the use, storage, sharing and analysis of huge volumes of data, especially in high-biodiversity countries. More studies comparing the relative efficiency and cost-effectiveness of different tools with different species in different habitats would help managers choose the right tools for their needs and capacity and better integrate them into monitoring schemes. eDNA is becoming the go-to option for the monitoring of aquatic species diversity and community composition and has also proven successful in some terrestrial settings. eDNA is especially useful for monitoring species that are in low densities or difficult to observe with traditional observer-based methods; indeed, several studies show eDNA metabarcoding techniques have a much better detection probability overall for taxa such as amphibians and fish. In some cases, eDNA has been shown to complement other tools when used together, by either increasing animal detection probabilities or increasing the number of indicators that can be measured at one site. This suggests that, in future, more effort should be made to test the effectiveness of integrating eDNA with one or more other tools to enhance the efficiency and effectiveness of measuring indicators and to increase the diversity of species detected. For example, eDNA could be combined with camera traps for monitoring vertebrates visiting waterholes. Testing multiple tools would also provide better opportunity to quantify when and how traditional observer-based methods can complement the technological solutions and when they are more cost-effective. However, it is noteworthy that, in general, the taxa for which data are most lacking, such as invertebrates, plants and fungi, are still those less easily monitored by eDNA and other new technologies. This suggests a focus only on technological solutions for biodiversity monitoring may perpetuate existing taxonomic data biases. I conclude by discussing the international policy context and the relevance of eDNA for monitoring global biodiversity indicators. Several opportunities exist to integrate eDNA into monitoring programmes to measure government, business and civil society contributions towards delivery of the post-2020 global biodiversity framework and the Sustainable Development Goals.


2016 ◽  
Vol 25 (4) ◽  
pp. 929-942 ◽  
Author(s):  
Alice Valentini ◽  
Pierre Taberlet ◽  
Claude Miaud ◽  
Raphaël Civade ◽  
Jelger Herder ◽  
...  

2016 ◽  
Author(s):  
Philip Francis Thomsen ◽  
Steffen Sanvig Bach ◽  
Eva Sigsgaard ◽  
Peter Rask Moeller

2021 ◽  
Vol 171 ◽  
pp. 112786
Author(s):  
Vignesh Kumar Balasubramanian ◽  
Midhuna Immaculate Joseph Maran ◽  
Darwin Ramteke ◽  
Deepak Samuel Vijaykumar ◽  
Abhilash Kottarathail Rajendran ◽  
...  

2018 ◽  
Author(s):  
Noémie Leduc ◽  
Louis Bernatchez ◽  
Philippe Archambault ◽  
Kimberly Howland ◽  
Antoine Dispas ◽  
...  

Arctic biodiversity has been for a long time underestimated, situated in a region considered as an austere environment combined to the lack of knowledge. The analysis of environmental DNA (eDNA), a new method tracing DNA from macro-organisms, is changing the way we monitor aquatic biodiversity and has the potential to answer large-scale fundamental biodiversity questions in remote regions such as the Arctic. This study aims to evaluate the eDNA dispersal by contrasting the difference between eDNA metabarcoding and classical sampling methods of the alpha, beta and gamma biodiversity index across the Canadian Arctic latitudinal gradient. Water samples of 250mL were collected in 13 sites within three Arctic ports: Churchill, Iqaluit and Deception Bay. Our results showed a species richness of 422 marine invertebrates, while the number of species detected decreased with latitude with more than 100 less species in the northern port. Contrasting the alpha biodiversity index between eDNA metabarcoding and species spatial distribution may be used to evaluate the eDNA spatial dispersion, thus answering important questions related to the ecology of eDNA and improving the integration of this new molecular tool within applied sciences.


Author(s):  
Toshiaki Jo ◽  
Hiroki Yamanaka

Environmental DNA (eDNA) analysis is a promising tool for non-disruptive and cost-efficient estimation of species abundance. However, its practical applicability in natural environments is limited owing to a potential gap between eDNA concentration and species abundance in the field. Although the importance of accounting for eDNA dynamics, such as transport and degradation, has been discussed, the influence of eDNA characteristics, including production source and cellular/molecular state, on the accuracy of eDNA-based abundance estimation was entirely overlooked. We conducted meta-analyses using 44 of previous eDNA studies and investigated the relationships between the accuracy (R) of eDNA-based abundance estimation and eDNA characteristics. First, we found that estimated R values were significantly lower for crustaceans and mussels than fish. This finding suggests that less frequent eDNA production of these taxa owing to their external morphology and physiology may impede accurate estimation of their abundance via eDNA. Moreover, linear mixed modeling showed that, despite high variances, R values were positively correlated with filter pore size, indicating that selective collection of larger-sized eDNA, which is typically fresher, could improve the estimation accuracy of species abundance. Although our collected dataset was somewhat biased to the studies targeting specific taxa, our findings shed a new light on the importance of what characteristics of eDNA should be targeted for more accurate estimation of species abundance. Further empirical studies are required to validate our findings and fully elucidate the relationship between eDNA characteristics and eDNA-based abundance estimation.


2017 ◽  
Vol 74 (12) ◽  
pp. 2030-2034 ◽  
Author(s):  
Stephen L. Klobucar ◽  
Torrey W. Rodgers ◽  
Phaedra Budy

Environmental DNA (eDNA) sampling has proven to be a valuable tool for detecting species in aquatic ecosystems. Within this rapidly evolving field, a promising application is the ability to obtain quantitative estimates of relative species abundance based on eDNA concentration rather than traditionally labor-intensive methods. We investigated the relationship between eDNA concentration and Arctic char (Salvelinus alpinus) abundance in five well-studied natural lakes; additionally, we examined the effects of different temporal (e.g., season) and spatial (e.g., depth) scales on eDNA concentration. Concentrations of eDNA were linearly correlated with char population estimates ([Formula: see text] = 0.78) and exponentially correlated with char densities ([Formula: see text] = 0.96 by area; 0.82 by volume). Across lakes, eDNA concentrations were greater and more homogeneous in the water column during mixis; however, when stratified, eDNA concentrations were greater in the hypolimnion. Overall, our findings demonstrate that eDNA techniques can produce effective estimates of relative fish abundance in natural lakes. These findings can guide future studies to improve and expand eDNA methods while informing research and management using rapid and minimally invasive sampling.


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