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Impact of storage conditions on the preservation of taphonomically altered human skeletal remains

Insights from ATR-FTIR spectroscopy and DNA analysis

Bibliographic Data

ID4683136
AuthorsTamara Leskovar (0000-0002-4585-4726, University of Ljubljana), Ivan Jerman (0000-0003-4476-3571, National Institute of Chemistry), Irena Zupanič Pajnič (0000-0002-6704-015X, University of Ljubljana, corresponding author)
Year2025
Volume73
Pages371-381
Publication date2025-05-01
Peer ReviewedYes
Open AccessYes
TypeARTICLE
VenueJournal of Cultural Heritage (JOURNAL)
Journal identifiersISSN: 1296-2074 • E-ISSN: 1778-3674
PublisherElsevier BV (PUBLISHER)
DOI10.1016/j.culher.2025.04.011
OpenAlexW4409972219
LanguageEN
Citations received1
References cited92

The effects of storage conditions on bone samples are substantial. • Changes in DNA at room temperature were linked to mineral and collagen alterations. • Changes in DNA in the freezer were associated with changes in mineral. • Freezer storage mitigates degradation by minimizing mineral and collagen loss. • Room-temperature accelerates changes, particularly in collagen quality and quantity. The preservation of skeletonised human remains is crucial for successful archaeological and forensic analyses, yet it is influenced by various intrinsic and extrinsic factors. While numerous studies have addressed preservation states and their implications, the effects of storage conditions on taphonomically altered remains have been largely overlooked. This study examines the impact of storage conditions—freezer and room temperature—on bone samples from 21 femur shafts excavated from a World War II mass grave over a period of 1, 2, and 3 years. Changes were analysed using ATR-FTIR spectroscopy and DNA analysis to explore correlations between molecular alterations and DNA preservation. Results demonstrate that storage conditions significantly affect bone preservation. Freezer storage showed minimal degradation, primarily characterised by changes in mineral crystallinity due to the loss of loosely bound ions, while collagen quality improved initially, likely due to molecular reordering. In contrast, room-temperature storage accelerated both mineral and collagen deterioration, with pronounced effects on collagen quantity and quality correlating with increased crystallinity and apatite domain proportions. DNA quality and quantity exhibited similar trends under both conditions, though correlations with mineral and collagen changes varied by storage environment. Over three years, freezer storage mitigated degradation by limiting mineral and collagen loss, whereas room-temperature storage accelerated changes, especially in collagen. These findings highlight the importance of controlled storage conditions, as significant molecular and structural alterations were observed within a relatively short period. This has important implications for the long-term preservation of forensic and archaeological samples, emphasising the need for appropriate storage strategies to ensure sample integrity for future analyses

DNA · Fourier transform infrared spectroscopy · Physics · Archaeology and ancient environmental studies · Chemical Engineering · Chemistry · Engineering · Forensic Anthropology and Bioarchaeology Studies · Materials Science · Pleistocene-Era Hominins and Archaeology · Biochemistry · Spectroscopy

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