Do All Animals Have a Microbiome? A Research Guide
From the guts of elephants to the tissues of coral reefs, scientists are uncovering a hidden yet essential world: the animal microbiome. As research...
4 min read
Manoj Dadlani
:
Oct 13, 2025 5:43:27 AM
Environmental DNA (eDNA) sampling for species identification has revolutionized biodiversity monitoring by enabling highly accurate, cost-effective, non-invasive detection of organisms across aquatic, terrestrial, and atmospheric environments.
As biodiversity monitoring continues to evolve, eDNA sampling for species identification provides a transformative tool for researchers, conservationists, and environmental managers. By extracting genetic material from environmental samples such as water, soil, and air, eDNA metabarcoding and qPCR analysis can rapidly detect target species, assess community composition, and inform conservation interventions without direct organism handling.
At Cmbio, we support this evolving field through cutting-edge eDNA Metabarcoding Research and analysis.
This blog examines multiple applications, data points, and integration strategies across environments, answering the key questions: how do eDNA methods work, and how do they compare to traditional approaches in detection rates, accuracy, cost and time.
Water-based eDNA approaches rely on filtration of 1-2 liters using 0.7 μm glass fiber filters, capturing molecular traces from fish, invertebrates, and other aquatic taxa for qPCR and metabarcoding analysis targeting COI and 18S markers.
Cmbio’s suite of eDNA, genomics, and bioinformatics services prepare policy-makers, regulators, and conservationists for rapid, scalable, and evidence-led biodiversity monitoring.
eDNA detection utilizes molecular techniques to survey organisms by collecting genetic traces from water, soil, or air, often detecting target species at much lower population densities than conventional field sampling. When using eDNA, research routinely demonstrates higher sensitivity: more than 94% detection rates and reduced false negatives in aquatic environments, especially for cryptic or low-abundance organisms. The process is non-invasive and quick, enabling sampling in areas where visual or capture methods are impractical, and standardized protocols (gloves, field blanks, new tubes per site, interval sampling for large areas) greatly minimize contamination risks.
Yes, using eDNA enables reliable detection of rare species through targeted qPCR and metabarcoding, supporting biodiversity assessments, conservation monitoring, and ecological research. eDNA collection protocols (such as filtering water or sampling soil from suitable habitats) have consistently revealed species that remain undetected in standard surveys, including critically endangered fish and elusive amphibians. The potential for detection depends on sampling design (e.g., site selection, frequency, primer specificity) and ecological factors like species secretion rates, water flow, and DNA degradation, all of which affect eDNA concentration and detection reliability.
eDNA field sampling supports multi-species identification in a single collection by employing broad-range or multiple primer sets to amplify genetic material from various taxa (fish, plants, invertebrates, and even microbes) in the same sample. A single eDNA collection (such as a filtered water or bulk soil sample) can be split for several analyses, delivering full community profiles and enhanced biodiversity monitoring potential. Stored extracts allow for additional species targeting long after initial collection, making eDNA strategies highly scalable for environmental surveys, restoration projects, and compliance reporting. Field protocols recommend interval sampling, repetition, and careful documentation to maximize accuracy and compare results across locations.
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