4.3 Article

Experimentally Derived Sedimentary, Molecular, and Isotopic Characteristics of Bone-Fueled Hearths

Journal

JOURNAL OF ARCHAEOLOGICAL METHOD AND THEORY
Volume 26, Issue 4, Pages 1327-1375

Publisher

SPRINGER
DOI: 10.1007/s10816-019-09411-3

Keywords

Hearths; Bone burning; Biomarkers; Stable isotopes; Micromorphology; Lipids

Funding

  1. European Research Council

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Molecular and isotopic analysis of sediments from archaeological combustion features is a relatively new area of study. Applications can inform us about ancient pyro-technologies and patterns of animal exploitation in a wide range of human contexts, but may be particularly informative with regard to ancient hunter-gatherers. Our analyses of sediments from experimental bone and wood fires, and from controlled laboratory heating sequences, provide fine-grained data on the formation and location of biomarkers from pyrolyzed animal fats in hearths. Integrating microstratigraphic, molecular, and isotopic data can improve recognition of bone fires in archaeological contexts, perhaps even where bone preservation is poor. Experimental bone fires produced an upper layer of calcined bone above a thin layer of tarry black amorphous material coating mineral sediments. Mineral sediments beneath the black layer showed little alteration but high lipid content. Sampling for molecular and isotopic analysis should target the black layer as the bulk of pyrolyzed biomarkers are located here and stable isotope values are less affected than in the overlying layer of ash or calcined bone. The combined presence of certain symmetric and slightly asymmetric saturated long-chain ketones (14-nonacosanone, 16-hentriacontanone 16-tritriacontanone, and 18-pentatriacontanone), especially together with heptadecane (C(17)n-alkane), are molecular indicators of the thermal degradation of terrestrial animal fat. Formation and relative dominance of these molecules in hearth sediments relates to the initial prevalence of specific precursor fatty acids and can provide broad separations between sources. We suggest that separations could be further supported and expanded by combining stable isotope analysis of the same compounds.

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