Michael Bunce’s research while affiliated with Curtin University and other places

What is this page?


This page lists works of an author who doesn't have a ResearchGate profile or hasn't added the works to their profile yet. It is automatically generated from public (personal) data to further our legitimate goal of comprehensive and accurate scientific recordkeeping. If you are this author and want this page removed, please let us know.

Publications (280)


FIGURE 2 | Overview of all Australian (red) and New Zealand (blue) sites from which samples of southern elephant seal (Mirounga leonina) were obtained for ancient DNA analysis. Only sites with samples that yielded viable DNA are shown. Map lines delineate study areas and do not necessarily depict accepted national boundaries.
FIGURE 3 | Temporally aware haplotype network showing the relationships among haplotypes of southern elephant seal (Mirounga leonina) for five time periods. Haplotypes are represented as ellipses, coloured by location. Ellipse size represents haplotype frequency. Lines link haplotypes separated by one mutation; dots represent additional mutations. Haplotypes absent in any particular timeframe are shown as white ellipses on that layer.
FIGURE 4 | Dated phylogenetic tree from Bayesian analysis of 23 mitochondrial genomes from southern elephant seals (Mirounga leonina; 10 ancient & 13 modern seals). Estimates of divergence times were calibrated using the radiocarbon dates of ancient mitochondrial genomes, along with a previous estimate of the mutation rate for the mitochondrial control region (HVR1) (de Bruyn et al. 2009). Light blue bars indicate 95% credibility intervals of age estimates. Nodes are labelled with posterior probabilities. Sex of the individual is shown where known. Inset shows a mummified southern elephant seal, which previously yielded ancient DNA, from the now extinct Victoria Land Coast population (de Bruyn et al. 2009).
Postglacial Recolonization of the Southern Ocean by Elephant Seals Occurred From Multiple Glacial Refugia
  • Article
  • Full-text available

March 2025

·

80 Reads

Global Change Biology

Andrew A Berg

·

Megan Askew

·

·

[...]

·

The Southern Ocean is warming more rapidly than other parts of our planet. How this region's endemic biodiversity will respond to such changes can be illuminated by studying past events through genetic analyses of time‐series data sets, including historic and fossil remains. Archaeological and subfossil remains show that the southern elephant seal ( Mirounga leonina ) was common along the coasts of Australia and New Zealand in the recent past. This species is now mostly confined to sub‐Antarctic islands and the southern tip of South America. We analyzed ancient seal samples from Australia (Tasmania), New Zealand and the Antarctic mainland to examine how southern elephant seals have responded to a changing climate and anthropogenic pressures during the Holocene. Our analyses show that these seals formed part of a broader Australasian lineage, comprising seals from all sampled locations from the south Pacific sector of the Southern Ocean. Our study demonstrates that southern elephant seal populations have dynamically altered both range and population sizes under climatic and human pressures over surprisingly short evolutionary timeframes for such a large, long‐lived mammal.

Download

Postglacial recolonization of the Southern Ocean by elephant seals occurred from multiple glacial refugia

November 2024

·

159 Reads

The Southern Ocean is warming more rapidly than other parts of our planet. How this region’s endemic biodiversity will respond to such changes can be illuminated by studying past events, through genetic analyses of time-series data sets including historic and fossil remains. Archaeological and subfossil remains show that the southern elephant seal ( Mirounga leonina ) was common along the coasts of Australia and New Zealand in the recent past. This species is now mostly confined to sub-Antarctic islands and the southern tip of South America. We analysed ancient seal samples from Australia (Tasmania), New Zealand, and the Antarctic mainland to examine how southern elephant seals have responded to a changing climate and anthropogenic pressures during the Holocene. Our analyses show that these seals formed part of a broader Australasian lineage, comprising seals from all sampled locations from the south Pacific sector of the Southern Ocean. Our study demonstrates that southern elephant seal populations have dynamically altered both range and population sizes under climatic and human pressures, over surprisingly short evolutionary timeframes for such a large, long-lived mammal. Significance Statement Genetic data, alongside historic, archaeological, and subfossil remains show that Australasian populations of the southern elephant seal have been shaped by range expansions and contractions following the Last Glacial Maximum, with subsequent contractions during the late Holocene. These expansion and contraction events are likely to have been a direct result of climate change-induced habitat expansion and contraction, along with Indigenous and European sealing. Prehistoric climate change and more recent human pressures have substantially altered the geographic distribution and population size of southern elephant seals over short evolutionary timescales.


eDNA metabarcoding captures a decline of coral diversity at Taiping Island after an outbreak of Crown-of-Thorns starfish

September 2024

·

183 Reads

Coral Reefs

Coral reefs are known to be one of the most diverse marine ecosystems on earth. However, these important ecosystems are heavily stressed by natural and anthropogenic activities. Environmental DNA (eDNA) metabarcoding is an innovative approach that can provide a greater diversity of taxonomic detections, non-invasive sampling, and a lower field component cost than traditional biomonitoring methods. Taiping Island (Itu Aba Island) is one of the major coral reef islands situated in the South China Sea where underwater visual surveys documented an outbreak of Crown-of-Thorns starfish (COTS) in 2021. In our study, we used eDNA metabarcoding to investigate whether there were shifts in coral communities by comparing pre- and post-COTS outbreak communities. One metabarcoding assay targeting the 18S gene and two assays targeting the ITS2 region (one of these assays specifically targeting Acroporid corals) were applied to 42 seawater samples collected in 2019 and 2021 from 12 sites around Taiping Island. Based on these three metabarcoding assays, 52 unique hard coral species were identified, corresponding to a total of 51 species in 2019 and 26 species in 2021. Our results indicated a significant decline in coral diversity but an increase in sponge diversity from the phylum porifera at Taiping Island in 2021. We suggest that these faunal shifts may be due to active feeding and disturbance of COTS at outbreak proportions that result in habitat changes. Our findings also suggest that eDNA can continue to serve as a promising tool to monitor the change in coral as well as reef-associated taxa during devastating outbreak events.



A generalised overview of IMS detection by different example eNA analysis technologies with a workflow indicated by blue arrows. A Collection of eNA is the first step in any IMS detection procedure. Sampling can be by filtering water (e.g. Stat et al. 2017), passive methods (e.g. Bessey et al. 2021; Cai et al. 2022), natural passive sampling systems like sponges (Mariani et al. 2019; Jeunen et al. 2023), and direct sampling of biofilms and other material from stationary substrates (e.g. Koziol et al. 2019). The mixed biological and mineral material that these methods collect contains large amounts of eNA from live microbial communities as well as small quantities of DNA and RNA shed from macro organisms, as tissue chunks, single, or degraded cells (Mauvisseau et al. 2022). B Targeted species detection technologies allow IMS to be detected in the purified eDNA (see Berry et al. 2021). Detection of pre-defined IMS by a specialised testing procedure is commonly done by qPCR (quantitative Polymerase Chain Reaction) (e.g. Gargan et al. 2022) or ddPCR methods (Doi et al. 2015). These approaches have advantages of being high throughput and sensitive, but will only detect one IMS that is pre-defined for each test (Manfrin et al. 2022). Field-deployable tests are possible, but not widely applied currently (e.g. Baerwald et al. 2020). C DNA metabarcoding is the method of PCR amplifying a small DNA region that varies in sequence among species. The unique DNA barcode sequences can be determined for a range of species in parallel using high throughput DNA sequencing technology. The range of species that DNA metabarcoding can detect is determined by how many test groups are analysed. For example, in the IMS context, invasive fish might be the only group of interest, and a single eDNA metabarcoding test might be used to identify many fish (e.g. Jo et al. 2022). The “Tree of life’ eDNA metabarcoding approach is to run a wide range of eDNA tests on each eDNA sample to attempt to identify as much of the biodiversity represented in the eDNA as possible (Stat et al. 2017; Adams et al. 2023)
A section of the notes taken from discussions organised to link similar themes arising in discussion. The top linking theme of this discussion was education. Discussion points on sub-themes are indicated by a shared colour
Research horizons for invasive marine species detection with eDNA/eRNA

July 2024

·

177 Reads

·

1 Citation

Biological Invasions

The global marine ecosystem is changing rapidly as the result of biogeochemical cycles and ecosystem structure being altered by industrial civilization. Invasive marine species (IMS) are one of the most damaging regional consequences of human activity, and one of the most easily attributable to specific processes. This makes IMS introduction one of most tractable threats for management by appropriate policies. Once established, a different set of policies are required either to restrict IMS spread, or to attempt local eradication. The key ecosystem management tool for IMS damage mitigation is rapid, widely deployable IMS detection. Environmental Nucleic Acids (eNA), combining environmental DNA (eDNA) and environmental RNA (eRNA) analyses, have emerged as valuable tools for sensitive, cost-effective and readily deployable detection of IMS. Methods for IMS detection by eNA are still being developed through a widespread and active research community, so identifying the limitations of current processes will help prioritise eNA-based IMS detection research. We analysed and synthesised the opinions of expert marine ecosystem managers and researchers in Australia and New Zealand about the knowledge gaps and research needs for eNA-based IMS detection. This synthesis was placed in context with current research literature on what eNA technologies are currently providing as an IMS management tool; what problems exist with the current technology; and what could be done to improve this general approach. Our analyses produced a list of priorities that chart a path towards the best possible systems for IMS detection by eNA.


Quantifying wildlife conflicts with metabarcoding and traditional dietary analyses: applied to seabird predation by long-nosed fur seals

May 2024

·

92 Reads

Wildlife conflicts require robust quantitative data on incidence and impacts, particularly among species of conservation and cultural concern. We apply a multi-assay framework to quantify predation in a southeastern Australian scenario where complex management implications and calls for predator culling have grown despite a paucity of data on seabird predation by recovering populations of long-nosed fur seals (Arctocephalus forsteri). We apply two ecological surveillance techniques to analyze this predator’s diet – traditional morphometric (prey hard-part) and environmental DNA metabarcoding (genetic) analyses using an avian specific primer for the 12S ribosomal RNA (rRNA) gene – to provide managers with estimated predation incidence, number of seabird species impacted and inter-prey species relative importance to the predator. DNA metabarcoding identified additional seabird taxa and provided relative quantitative information where multiple prey species occur within a sample; while parallel use of both genetic and hard-part analyses revealed a greater diversity of taxa than either method alone. Using data from both assays, the estimated frequency of occurrence of predation on seabirds by long-nosed fur seals ranged from 9.1–29.3% of samples and included up to 6 detected prey species. The most common seabird prey was the culturally valued little penguin (Eudyptula minor) that occurred in 6.1–25.3% of samples, higher than previously reported from traditional morphological assays alone. We then explored DNA haplotype diversity for little penguin genetic data, as a species of conservation concern, to provide a preliminary estimate of the number of individuals consumed. Polymorphism analysis of consumed little penguin DNA identified five distinct mitochondrial haplotypes – representing a minimum of 16 individual penguins consumed across 10 fur seal scat samples (equivalent to 10.1% of samples). We recommend rapid uptake and development of cost-effective genetic techniques and broader spatiotemporal sampling of fur seal diets to further quantify predation and hotspots of concern for wildlife conflict management.


A) Study site showing location of three mine sites and the locations of the different infrastructure types at each site, where MT is Maintained Track, Pad is Drill Pad, and UT is Unmaintained track B) Stylised image of experimental design and pitfall trap placement along each transect across the ecotone between the disturbance (maintained track, unmaintained track, or drill pad) and remnant vegetation. The grey dashed lines indicate prospective topographic lines
Principal component analysis (PCA) plot of the habitat characteristics at each site showing the three different infrastructure types where MT is Maintained Track, Pad is Drill Pad, and UT is Unmaintained track. Trajectories are overlaid starting from Quadrat i (1) on the disturbance to Quadrat vi (6) approximately 100 m into the remnant vegetation. Vectors overlaid of the correlation between each habitat characteristic and the principal component axes. The circle is a unit circle (radius = 1.0), used to illustrate the nature and strength of the correlation
zOTU richness at the different quadrat locations (Quadrat Number i-vi) at the different sites and infrastructure types for the (A) overall arthropod communities, (B) Formicidae communities, and (C) Collembola communities. Sites are notated as KA for Karara, KO for Koolanooka, and MG for Mount Gibson. Different infrastructure types and sites are highlighted where MT is Maintained Track, Pad is Drill Pad, and UT is Unmaintained track
Non-metric multidimensional scaling (NMDS) plots showing (A) overall arthropod communities, (B) Formicidae communities, and (C) Collembola communities at the three sites. Sites are notated as KA for Karara, KO for Koolanooka, and MG for Mount Gibson. Different infrastructure types and sites are highlighted where MT is Maintained Track, Pad is Drill Pad, and UT is Unmaintained track
Non-metric multidimensional scaling (NMDS) plots showing the (A) arthropod communities, (B) Formicidae communities, and (C) Collembola communities at the three sites. Different infrastructure types are colour coded where MT is Maintained Track, Pad is Drill Pad, and UT is Unmaintained track. Trajectories are overlaid starting from Quadrat i (1) to Quadrat vi (6)
Mining exploration infrastructure affects biophysical habitat characteristics and ground-dwelling arthropod communities

May 2024

·

60 Reads

Biodiversity and Conservation

Monitoring of environmental impacts of mining activities typically focuses on the main operation footprint, neglecting exploration infrastructure like tracks, roads, and drill pads. These areas are cleared of native vegetation and impacts on the surrounding environment can be both cumulative and enigmatic. Here, we study the impacts of mining exploration infrastructure on habitat characteristics and ground-dwelling arthropod communities in the Midwest region of Western Australia. The study was conducted at three mine sites, each with three infrastructure types: maintained tracks, unmaintained tracks, and drill pads along transects extending 100 m away from the disturbance into remnant vegetation. Habitat characteristics were measured, and arthropods collected from pitfall traps along these transects and identified using COI metabarcoding. The overall arthropod community and two indicator groups, ants (Formicidae) and springtails (Collembola) - were used to measure arthropod responses to changes in response to habitat disturbance. Whilst changes in habitat were only visible to 10 m from the disturbance, impacts on arthropod communities could be detected up to 100 m into the remnant vegetation, and these responses were more complex. In general, we found similar patterns expressed in the compositional changes for arthropods overall and between our chosen indicator groups, but they were not the same across all sites and infrastructure types. Our results demonstrate the utility of bulk arthropod metabarcoding and different arthropod indicator groups for documenting the effects of fine-scale habitat destruction, degradation, or disturbance. They also highlight the need to monitor the negative impacts of mineral exploration on the environment.


(a) Map of Perth Zoo showing the locations of carrion fly traps within the zoo (Z1–Z6). Major ‘animal zones’ designated by Perth Zoo that correspond to the groups of animals kept within the zoo are illustrated in colour with corresponding labels: African Savannah, Asian Rainforest and Australian Animals. Animal enclosures where the fly traps were put into are included in colour, other zoo animals detected in this study are indicated as black silhouettes, and zoo animals located in the same animal zone but not detected are shown as grey silhouettes. Prevailing wind directions are marked as blue arrows. (b) Map showing the sampling locations (dark blue circles) spaced approximately 250 m apart along 4 km transects away from Perth Zoo (16 sampling locations per transect). The inset map shows the locations of the fly traps within the zoo. Prevailing wind directions are marked as blue arrows. Inset image shows a carrion fly sampler with pop-out diagram of the trap construction. Diagram created with Biorender.com.
Species accumulation curves for zoo and wild animals detected from carrion flies caught at samples within the zoo (blue triangle), and all samples collected from all samples (orange circle). (a) Sample size-based rarefaction and extrapolation sampling curve. (b) Sample completeness curve.
Number of sequences of the four zoo-resident mammal species detected both in the zoo (inset) and along the transects: (a) Panthera leo (lion), (b) Lycaon pictus (African painted dog), (c) Hylobates moloch (Javan gibbon) and (d) Saguinus oedipus (cotton-top tamarin). The colour of the circles indicates the total number of sequences detected from samples at the transect point across all sampling days. Silhouettes of the detected animals are included.
Analysing the effects of distance, taxon and biomass on vertebrate detections using bulk-collected carrion fly iDNA

April 2024

·

134 Reads

Invertebrate-derived DNA (iDNA) metabarcoding from carrion flies is a powerful, non-invasive tool that has value for assessing vertebrate diversity. However, unknowns exist around the factors that influence vertebrate detections, such as spatial limits to iDNA signals or if detections are influenced by taxonomic class or estimated biomass of the vertebrates of interest. Using a bulk-collection method, we captured flies from within a zoo and along transects extending 4 km away from this location. From 920 flies, we detected 28 vertebrate species. Of the 28 detected species, we identified 9 species kept at the zoo, 8 mammals and 1 bird, but no reptiles. iDNA detections were highly geographically localized, and only a few zoo animals were detected outside the zoo setting. However, due to the low number of detections in our dataset, we found no influence of the taxonomic group or the estimated biomass of animals on their detectability. Our data suggest that iDNA detections from bulk-collected carrion flies, at least in urban settings in Australia, are predominantly determined by geographic proximity to the sampling location. This study presents an important step in understanding how iDNA techniques can be used in biodiversity monitoring.


TICI: a taxon-independent community index for eDNA-based ecological health assessment

February 2024

·

184 Reads

·

14 Citations

Global biodiversity is declining at an ever-increasing rate. Yet effective policies to mitigate or reverse these declines require ecosystem condition data that are rarely available. Morphology-based bioassessment methods are difficult to scale, limited in scope, suffer prohibitive costs, require skilled taxonomists, and can be applied inconsistently between practitioners. Environmental DNA (eDNA) metabarcoding offers a powerful, reproducible and scalable solution that can survey across the tree-of-life with relatively low cost and minimal expertise for sample collection. However, there remains a need to condense the complex, multidimensional community information into simple, interpretable metrics of ecological health for environmental management purposes. We developed a riverine taxon-independent community index (TICI) that objectively assigns indicator values to amplicon sequence variants (ASVs), and significantly improves the statistical power and utility of eDNA-based bioassessments. The TICI model training step uses the Chessman iterative learning algorithm to assign health indicator scores to a large number of ASVs that are commonly encountered across a wide geographic range. New sites can then be evaluated for ecological health by averaging the indicator value of the ASVs present at the site. We trained a TICI model on an eDNA dataset from 53 well-studied riverine monitoring sites across New Zealand, each sampled with a high level of biological replication ( n = 16). Eight short-amplicon metabarcoding assays were used to generate data from a broad taxonomic range, including bacteria, microeukaryotes, fungi, plants, and animals. Site-specific TICI scores were strongly correlated with historical stream condition scores from macroinvertebrate assessments (macroinvertebrate community index or MCI; R ² = 0.82), and TICI variation between sample replicates was minimal (CV = 0.013). Taken together, this demonstrates the potential for taxon-independent eDNA analysis to provide a reliable, robust and low-cost assessment of ecological health that is accessible to environmental managers, decision makers, and the wider community.


Research horizons for invasive marine species detection with eDNA/eRNA

November 2023

·

201 Reads

The global marine ecosystem is changing rapidly as the result of biogeochemical cycles and ecosystem structure being altered by industrial civilization. Invasive marine species (IMS) are one of the most damaging regional consequences of human activity, and one of the most easily attributable to specific processes. This makes IMS introduction one of most tractable threats for management with appropriate policies. Once established, a different set of policies are required either to restrict IMS spread, or to attempt local eradication. The key ecosystem management tool for IMS damage mitigation is rapid, widely deployable IMS detection. Environmental Nucleic Acids (eNA), combining environmental DNA (eDNA) and environmental RNA (eRNA) analyses, have emerged as valuable tools for sensitive, cost-effective and readily deployable detection of IMS. Methods for IMS detection by eNA are still being developed through a widespread and active research community, so identifying the limitations of current processes will help prioritise eNA-based IMS detection research. We analysed and synthesised the opinions of expert marine ecosystem managers and researchers in Australia and New Zealand about the knowledge gaps and research needs for eNA-based IMS detection. This synthesis was placed in context with current research literature on what eNA technologies are currently providing as an IMS management tool; what problems exist with the current technology; and what could be done to improve this general approach. Our analyses produced a list of priorities that chart a path towards the best possible systems for IMS detection by eNA - the eNA Utopia.


Citations (73)


... While eDNA can show which species are present, eRNA can reveal which organisms are actively functioning in the ecosystem [47]. Combining these methods could improve our understanding of how species contribute to ecosystem health [48,49]. Furthermore, there is no development of specific primers to detect Indonesia's unique species or monitor invasive species, despite the country's rich biodiversity. ...

Reference:

Bibliometric analysis: Environmental DNA (eDNA) methods in marine biodiversity research in the world and Indonesia
Research horizons for invasive marine species detection with eDNA/eRNA

Biological Invasions

... The Wilderlab 'basic freshwater panel' uses five primer combinations to amplify small (~ 100 bp) fragments of 12S, 16S and COI, and targets invertebrates, mammals and fish (https://wilderlab.co.nz/). DNA extraction, PCR and sequencing methods followed those of Wilkinson et al. (2024), and were undertaken in a sterile, compartmentalised laboratory setting. Details of primer sequences and annealing temperatures are provided in the Supporting information. ...

TICI: a taxon-independent community index for eDNA-based ecological health assessment

... Barcoding uses species-specific primers to detect DNA fragments of a single species within a sample [141], while metabarcoding uses universal primers to detect millions of DNA fragments from various species [142]. This technique has been commonly used in aquatic ecosystems to assess biodiversity, such as in fish, amphibians [143], and bacterial antibiotic resistance genes (ARGs) [144]. Terrestrial ecosystems have also been assessed using eDNA, including terrestrial vertebrate diversity and global plant diversity using soil eDNA and pollen DNA [145,146]. ...

Gut content metabarcoding of specialized feeders is not a replacement for environmental DNA assays of seawater in reef environments Distributed under Creative Commons CC-BY 4.0

... m (Figure 1), whereas we took eDNA samples at ~0.5 m depth. We used this sampling design because previous studies showed that eDNA from samples collected on the surface are representative of the water column in depths up to 90 m (Stoeckle et al. 2021;Saenz-Agudelo et al. 2024;Hoban, Bunce, and Bowen 2023). Even if there were differences across sampled depth, we were aiming to assess the complementarity of using eDNA from surface water which is logistically more accessible (i.e., an independent drop line is not required) and fast, rather than directly comparing BRUVS and eDNA from the same depth. ...

Plumbing the depths with environmental DNA ( eDNA ): Metabarcoding reveals biodiversity zonation at 45–60 m on mesophotic coral reefs
  • Citing Article
  • September 2023

Molecular Ecology

... eDNA metabarcoding has been applied to evaluate the impact of oil spills [12,21,23,24], and it has potential for application as a tool for benthic monitoring and identification of bioindicators of offshore oil and gas platforms [10,15,23]. Currently, eDNA is widely applied to assess overall community composition in aquatic ecosystems [20,25]. Indeed, the use of multi-taxa metabarcoding to assess the impact of offshore oil and gas platforms has recently been reported [10]. ...

Using environmental DNA to better inform decision making around decommissioning alternatives for offshore oil and gas infrastructure
  • Citing Article
  • August 2023

The Science of The Total Environment

... Carrion-breeding flies are thus tied to most aspects of ecosystem function. Recently, carrion-breeding flies have shown considerable potential in the monitoring of mammals through DNA carried by invertebrates, iDNA (Massey et al. 2022;Fernandes et al. 2023). ...

Use of carrion fly iDNA metabarcoding to monitor invasive and native mammals

... This change would help to increase the number of detections for Cnidaria/Porifera, addressing a limitation of the eDNA approach compared to data from visual surveys conducted over longer periods (i.e. years versus months). Given sufficient time and funding, additional improvements could include incorporating more metabarcoding assays to enhance confidence in taxon detection and assignment (Alexander et al. 2020;McElroy et al. 2020;Berry et al. 2023). Moreover, establishing locally sourced DNA reference libraries would improve the resolution of taxonomic assignment (Dugal et al. 2022). ...

A 3‐year plankton DNA metabarcoding survey reveals marine biodiversity patterns in Australian coastal waters

... For these, the first representative of each order was assigned the code "SOG" and grafted onto the tree as a sister order, before adding the rest of the species within the extinct order. Aepyornithiformes were made sister to Apterygiformes (Mitchell et al. 2014;Grealy et al. 2023), Dinornithiformes to Tinamiformes (Mitchell et al. 2014), and Gastornithiformes to Galliformes (Worthy et al. 2017). The extinct family Sylviornithidae was considered to be within Galliformes, but sister to all other species in the order (Worthy et al. 2016(Worthy et al. , 2017. ...

Molecular exploration of fossil eggshell uncovers hidden lineage of giant extinct bird

... For better species matching, we recommend only retaining species identifications with a BLAST identity score greater than 98% as applied by several other studies (e.g. Alexander et al., 2023;Webster et al., 2020) -but which we prefer not to apply in this study in order to obtain the most exhaustive possible plant composition of the diets. It's true that we may miss species or new identifications because of this 98% threshold, but it enables future authors to obtain a more certain list of flower species, the benefit-risk balance being in favor of applying a threshold. ...

Comparing environmental DNA collection methods for sampling community composition on marine infrastructure
  • Citing Article
  • February 2023

Estuarine Coastal and Shelf Science

... It enables the identification of organisms based on the DNA they release into the environment through gametes, faeces and other excretion products, as well as shed cells, as opposed to capturing or visually surveying organisms. Furthermore, it can be used to detect individual species as well as entire communities and can be combined with abiotic data to investigate the environmental drivers of biodiversity (e.g., Adams et al., 2023;Murray et al., 2024). It has proven to be a cost-efficient and non-invasive technique for monitoring biodiversity in marine ecosystems (Adams et al., 2023;Bernatchez et al., 2024), including in the Arctic Ocean and its adjacent seas (Geraldi et al., 2024;Lacoursière-Roussel et al., 2018;Merten et al., 2023;Murray et al., 2024;Weydmann-Zwolicka et al., 2024). ...

Environmental DNA metabarcoding describes biodiversity across marine gradients

ICES Journal of Marine Science