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Ashcroft, T.

Publications and source records attributed to Ashcroft, T..

2 recordsLinked to original sources

Temporal persistence of vertebrate airborne environmental DNA in a natural open-air setting

Airborne environmental DNA (eDNA) is a promising tool for detecting a wide range of terrestrial taxa, including threatened and invasive species, from trace genetic material shed into the air. Yet, application of this technique in species management is constrained by a limited understanding of airborne eDNA ecology, including temporal persistence of signals in open-air environments. We investigated the temporal persistence of airborne eDNA in a natural outdoor setting, using the invasive Bennetts wallaby Notamacropus rufogriseus as a case study. We captured airborne eDNA from a single Bennetts wallaby carcass, deployed in an area where wallabies are otherwise not present. A total of 180 samples were collected, spanning the period before deploying the carcass, the 11 days it was on site, and for 32 days after its removal, at distances of 1, 10, and 100 metres using both active (fan-assisted) and passive (no fan) collection methods. Although overall detection rates were low, wallaby DNA was detectable up to 100 metres away shortly after the wallaby was introduced to the site and for up to three days after its removal. These findings indicate that airborne eDNA persists only briefly. Actively sampling air using battery-powered fans significantly improved detection rates relative to passive sampling. We demonstrate that airborne eDNA can detect individual organisms in outdoor environments, but reliable detection requires robust sampling and replication to capture rare, transient signals. By revealing how these signals persist over time, our findings provide a framework for optimizing field deployment and for distinguishing remnant DNA from new incursions.

molecular biology↗

Targeted Airborne eDNA Detection of Pest Wallabies: Effects of Sampler Type and Distance

Bennetts wallabies Notamacropus rufogriseus, introduced to New Zealand from Australia in the late 1800s, strongly exemplify the detection challenges posed by invasive terrestrial species that are rare, cryptic, and highly mobile. Across their invasive range, N. rufogriseus occupy large landscapes at low densities, making their surveillance challenging. Recent research has demonstrated that airborne environmental DNA (eDNA) can rapidly identify terrestrial vertebrate diversity in an area. Leveraging these findings, we investigate the utility of airborne eDNA for the targeted monitoring of N. rufogriseus, using a novel, probe-based quantitative PCR assay. The effects of filtration material, collection method (active versus passive), distance from the source, and environmental conditions were examined for their effects on airborne detection probability, using a captive population of wallabies in a controlled park setting. A total of 110 airborne samples were collected, 55 with active (battery-powered fan) samplers and 55 passive (non-powered) samplers, across six distinct experimental periods at distances of 0, 10, 100, and 1000 metres from the closest known source of wallaby DNA. Filters designed to capture coarse particles (>10 {micro}m) significantly improved detection rates and DNA recovery for actively collected samples, compared to filters targeting finer particles (1-10 {micro}m). Active samplers significantly outperformed passive samplers in overall detection rates, particularly at shorter ranges from the target. Distance from the source had a significant negative effect on detection probability. Detection rates declined sharply beyond 10 metres but remained possible up to 1 kilometre from the source for both collection methods. These findings demonstrate that airborne eDNA can detect terrestrial vertebrate species at ecologically relevant distances, supporting its potential for landscape-scale surveillance. Notably, these results underscore the importance of optimising sampler design when applying airborne eDNA for targeted species monitoring.

genetics↗