Journal
JOURNAL OF ARCHAEOLOGICAL SCIENCE
Volume 127, Issue -, Pages -Publisher
ACADEMIC PRESS LTD- ELSEVIER SCIENCE LTD
DOI: 10.1016/j.jas.2020.105321
Keywords
Ancient DNA; Zooarchaeology; Shotgun sequencing; X chromosome
Funding
- European Union's EU Framework Programme for Research and Innovation Horizon 2020 under Marie Curie Actions as part of ArchSci 2020 [676154]
- BaltHealth programme under BONUS (Art. 185) - EU
- Innovation Fund Denmark [6180-00001B, 6180-00002B]
- Forschungszentrum Julich GmbH
- German Federal Ministry of Education and Research [FKZ 03F0767A]
- Academy of Finland [311966]
- Swedish Foundation for Strategic Environmental Research (MISTRA)
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The study successfully utilized the dog nuclear genome for genetic sex identification in pinnipeds, accurately identifying individual sex with a high degree of reliability. By applying this method to a range of ancient pinniped samples, including walruses, grey seals, and harp seals, distinct male and female sex groups were identified, shedding light on the potential effects of human activities and environmental change on these animal populations.
Determining the proportion of males and females in zooarchaeological assemblages can be used to reconstruct the diversity and severity of past anthropogenic impacts on animal populations, and can also provide valuable biological insights into past animal life-histories, behaviour and demography, including the effects of environmental change. However, such inferences have often not been possible due to the fragmented nature of the zooarchaeological record and a lack of clear diagnostic skeletal markers. In this study, we test whether the dog (Canis lupus familiaris) nuclear genome is suitable for genetic sex identification in pinnipeds. We initially tested 72 contemporary ringed seal (Pusa hispida) genomes with known sex, using the proportion of X chromosome DNA reads to chromosome 1 DNA reads (i.e. chrX/chr1-ratio) to distinguish males from females. This method was found to be highly reliable, with the ratios clustering in two clearly distinguishable sex groups, allowing 69 of the 72 individuals to be correctly identified according to sex. Secondly, to determine the lower limit of DNA reads required for this method, a subset of the ringed seal genome data was randomly down-sampled. We found a lower threshold of as few as 5000 mapped DNA sequence reads required for reliable sex identification. Finally, applying this standard, sex identification was successfully carried out on a broad set of ancient pinniped samples, including walruses (Odobenus rosmarus), grey seals (Halichoerus grypus) and harp seals (Pagophilus groenlandicus). All three species showed clearly distinct male and female chrX/chr1 ratio groups, providing sex identification of 42-98% of the samples, depending on species and sample quality. The approach described in this study should aid in untangling the putative effects of human activities and environmental change on populations of pinnipeds and other animal species.
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