Evidence map›Paper›PMID 42132311›Full record

ArticleMolecular ecology resources2026

Evaluating the Molecular Potential and Interpretability of DNA in Historical Spirit Collection Media.

Rachel L Tulloch, Jack Rojahn, Linda E Neaves, Alejandro Trujillo-González, Clare E Holleley, Erin E Hahn

Abstract read
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Article in Molecular ecology resources, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Rachel L TullochNational Research Collections Australia, Commonwealth Scientific Industrial Research Organisation, Canberra, Australian Capital Territory, Australia.
Jack RojahnCentre for Conservation, Ecology and Genomics, Institute for Applied Ecology, University of Canberra, Canberra, Australian Capital Territory, Australia.
Linda E NeavesSchool of Environment and Conservation, Murdoch University, Murdoch, Western Australia, Australia.
Alejandro Trujillo-GonzálezCentre for Conservation, Ecology and Genomics, Institute for Applied Ecology, University of Canberra, Canberra, Australian Capital Territory, Australia.ORCID https://orcid.org/0000-0002-6376-4978
Clare E HolleleyNational Research Collections Australia, Commonwealth Scientific Industrial Research Organisation, Canberra, Australian Capital Territory, Australia.ORCID https://orcid.org/0000-0002-5257-0019
Erin E HahnNational Research Collections Australia, Commonwealth Scientific Industrial Research Organisation, Canberra, Australian Capital Territory, Australia.ORCID https://orcid.org/0000-0001-6459-9508

Funding

Centre for Biodiversity Analysis
6 · The paper itself

Abstract

Advancements in historical genomics increasingly leverage museum collections to study past ecosystems, species interactions and biodiversity. Formalin-fixed, ethanol-preserved specimens, once thought inaccessible to molecular analyses due to DNA degradation, are emerging as valuable genomic resources. If recoverable and reliably attributable, DNA within preservation media could provide a non-destructive alternative to conventional tissue sampling, with the potential to expand molecular access to valuable or irreplaceable specimens. We tested whether preservation media contains recoverable DNA suitable for taxonomic inference. We coupled passive adsorption and active filtration of specimen media with hot alkaline lysis DNA extraction followed by metabarcoding and shotgun metagenomics. DNA was recoverable across samples, including 41 of 61 (~67%) targets in a composite sample. However, detections were dominated by non-target taxa, indicating that preservation media retain a layered mixture of specimen-derived DNA and broader collection-level background. Detection success tracked with preservation chemistry (near-neutral pH and low residual formaldehyde) rather than specimen age. Method choice influenced detections: active filtration increased target detections but admitted more background; passive capture was sparser but more selective; shotgun sequencing retrieved broader vertebrate signals, including reptiles, but was heavily enriched for non-targets. Because both target and non-target taxa were often abundant, read-abundance cut-offs were unreliable for attribution. Spirit-media DNA is therefore best interpreted as a collection-level signal and a screening tool to identify jars with molecular potential (e.g., taxa of conservation or biosecurity interest), rather than as a definitive non-destructive proxy for specimen identity. Prioritising chemically favourable jars and implementing rigorous contamination controls should improve signal interpretability and help unlock the value of preservation media for historical genomics.

Indexed as

DNAPreservation, BiologicalSpecimen HandlingAnimalsDNA Barcoding, TaxonomicMetagenomicsMuseumsShotgun SequencingDNAarchival DNAbiodiversityformalinmetabarcodingmuseum genomicsnon‐destructive sampling

Identifiers

PMID42132311
PMCPMC13174089

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