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Updated: Mar 6, 2026

Robust DNA Isolation and High-throughput Sequencing Library Construction for Herbarium Specimens
Published on: March 8, 2018
Patterns of aDNA damage through time and environments-lessons from herbarium specimens.
Stefano Porrelli1, Alice Fornasiero2, Hong Phuong Le1
1Trait Diversity and Function, Royal Botanic Gardens, Kew, Kew Road, Richmond, TW9 3AE, London, United Kingdom.
Ancient DNA (aDNA) in herbarium specimens degrades faster than in prehistoric samples. Environmental factors at collection, not storage, significantly impact DNA decay rates.
Area of Science:
- Genomics
- Paleogenomics
- Botany
Background:
- Herbarium collections offer extensive historical biodiversity data but are underutilized for ancient DNA research.
- Understanding DNA preservation in these collections is key for optimizing ancient DNA studies and curation.
Purpose of the Study:
- To quantify DNA degradation in herbarium specimens.
- To identify factors influencing DNA preservation and decay rates over time.
Main Methods:
- Analysis of genomic data from 573 herbarium specimens across six plant species (Hordeum, Oryza) spanning 220 years.
- Standardized laboratory protocols and shotgun sequencing to quantify DNA fragmentation and deamination.
Main Results:
- Significant age-dependent DNA fragmentation observed, with decay rates ~8x faster than in moa bones.
- Environmental conditions at collection (temperature-genus interaction) were the primary drivers of DNA damage (cytosine deamination).
- No significant effect of sample storage conditions on DNA damage or degradation was found.
Conclusions:
- Climatic origin, preservation environment, taxonomic identity, and age influence DNA preservation in herbarium specimens.
- Museum collections offer valuable insights into DNA degradation dynamics due to standardized preservation.
- Findings can inform improved institutional preservation practices for long-term DNA stability.
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