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Environmental DNA allows for the collection of valuable biodiversity information across global ecosystems by taking advantage of one simple fact of life: all organisms shed their DNA, (via mucus, feces, exuviae, skin, hair, or reproductive cells, etc.), into the environment around them. This environmental DNA, or eDNA, can be easily captured and used to detect an organism’s recent presence in a location without the need for visual detection or capture. The likelihood of DNA detection depends on environmental conditions and the state of the DNA when it’s shed. UV radiation, microbial activity, high temperatures, heavy precipitation, low pH, and fast water currents can all influence the persistence and presence of DNA in the environment. DNA inside intact cells is less susceptible to degradation via these factors; free DNA may degrade more quickly. All of these factors affect how our lab collects and utilizes eDNA in a given environment.


How does our lab use eDNA ?


Future of eDNA

Air eDNA

Recent publications have demonstrated species detection by simply filtering DNA suspended in the air. A study conducted at the Copenhagen Zoo successfully detected numerous exhibit species, feed species, pest species, and wild species (Lynggaard et. al., 2022). Some preliminary successes with airDNA have prompted experimentation using existing air quality monitoring infrastructure (e.g. air-quality networks) (Clare et. al., 2022; Littlefair et. al., 2023). We look forward to expanding the use of airDNA in our own work related to invasive species detection in forested and agricultural ecosystems.

 

Flower eDNA

Flowers are now being utilized by some groups as a substrate that regularly collects DNA from pollinators and other terrestrial arthropod communities (Thomsen & Sigsgaard, 2019; Newton et. al., 2023). Studies that aggregated DNA from flowers have had success in detecting a range of arthropod species (pollinators, predators, parasitoids), and determining patterns in plant-insect interaction webs.