Isotopic evidence for long-distance connections of the AD thirteenth century Promontory caves occupants ...
The Promontory caves (Utah) and Franktown Cave (Colorado) contain high-fidelity records of short-term occupations by groups with material culture connections to the Subarctic/Northern Plains. This research uses Promontory and Franktown bison dung, hair, hide, and bone collagen to establish local bas...
| Main Authors: | , , , , , , , |
|---|---|
| Format: | Dataset |
| Language: | English |
| Published: |
Dryad
2020
|
| Subjects: | |
| Online Access: | https://dx.doi.org/10.7291/d18q23 https://datadryad.org/stash/dataset/doi:10.7291/D18Q23 |
| Summary: | The Promontory caves (Utah) and Franktown Cave (Colorado) contain high-fidelity records of short-term occupations by groups with material culture connections to the Subarctic/Northern Plains. This research uses Promontory and Franktown bison dung, hair, hide, and bone collagen to establish local baseline carbon isotopic variability and identify leather from a distant source. The ankle wrap of one Promontory Cave 1 moccasin had a δ13C value that indicates a substantial C4 component to the animal’s diet, unlike the C3 diets inferred from 171 other Promontory and northern Utah bison samples. We draw on a unique combination of multi-tissue isotopic analysis, carbon isoscapes, ancient DNA (species and sex identification), tissue turnover rates, archaeological contexts, and bison ecology to show that the high δ13C value was not likely a result of local plant consumption, bison mobility, or trade. Rather, the bison hide was likely acquired via long-distance travel to/from an area of abundant C4 grasses far to the ... : We analyzed the FS-305 moccasin ankle wrap specimen at the UCSC Paleogenomics ancient DNA laboratory (PGL) to (1) obtain a taxonomic identification, and (2) determine the sex of the animal. Working in the sterile laboratory facilities at the PGL, we washed the sample in ultra-pure water to remove soil from the exterior and then extracted DNA from 0.15g of tissue following the Dabney et al. (2013) tissue extraction protocol. We prepared two shotgun sequencing libraries following the Meyer and Kircher (2010) method. We labelled the libraries using dual indices with truseq sequencing adapters and, after transferring the PCRs to the modern DNA facility, amplified them with Kappa Hifi for 25 cycles. We pooled and sequenced the libraries across several Illumina Miseq 2x75bp runs. We used Seqprep2 and prinseq (v. 0.20.4) to remove adapters and merge reads, and aligned the resulting data to the nucleotide BLAST database using MEGAN (v. 6.18.0) to identify the taxonomic origin of the tissue. In addition and to ... |
|---|