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Bioapatite 14C Age of Giant Mammals from Brazil

Published online by Cambridge University Press:  09 February 2016

Alexander Cherkinsky*
Affiliation:
Center for Applied Isotope Studies, University of Georgia, 120 Riverbend Road, Athens, Georgia 30602, USA
Mário André Trindade Dantas
Affiliation:
Laboratório de Paleozoologia, Universida de Federal de Minas Gerais, Belo Horizonte, Brazil
Mario Alberto Cozzuol
Affiliation:
Laboratório de Paleozoologia, Universida de Federal de Minas Gerais, Belo Horizonte, Brazil
*
Corresponding author. Email: [email protected].

Abstract

We investigated the radiocarbon age and stable isotope composition of bioapatite from bone, enamel, and dentine material from 3 different species of extinct mammals in South America. Most samples of Eremotherium laurillardi, Toxodon platensis, and Notiomastodon platensis were collected in natural depressions located in the northeastern Brazilian provinces of Sergipe, Bahia, and Rio Grande do Norte. All samples studied were devoid of collagen, which had decomposed as a result of high microbiological activity in this tropical region. We have instead analyzed the bioapatite fraction of the samples, which was relatively well preserved even in these harsh tropical conditions. The mineral fraction of bone and tooth material does not usually undergo microbiological decomposition but may be exposed to isotopic exchange with environmental carbonates. The problem thus becomes one of separating the diagenetic carbonates without destroying the bioapatite. We offer a technique for removing the secondary diagenetic carbonates by treatment with diluted acetic acid in a vacuum. We also demonstrate that proper pretreatment of bone and tooth samples allows the separation of diagenetic carbonates from bioapatite, as long as the carbon in these samples has not degraded completely. Bone, enamel, and dentine samples from individuals of the 3 mammalian species were dated using this technique and were compared to results by other researchers from the literature. Date ranges for the species presented were in good agreement with prior research. A comparison with other dating techniques such as U/Th and ESR shows the reliability of the treatment described and the feasibility of 14C dating the bioapatite fraction given certain conditions. In 2 cases, we dated bone enamel and dentine samples from the same individuals of N. platensis, with results between 14 and 21 ka. Results from dating samples of T. platensis are between 11.5 and 13 ka. The oldest tissue in both cases was dentine. The dating of enamel and dentine from the same species did not show regular differences; however, more often the dentine material was older. The oldest date, ≃22.5 ka for E. laurillardi, was obtained on the bioapatite fraction of dentine.

Type
Articles
Copyright
Copyright © 2013 by the Arizona Board of Regents on behalf of the University of Arizona 

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References

Ambrose, SN, Krigbaum, J. 2003. Bone chemistry and bioarchaeology. Journal of Anthropological Archaeology 22(3):193–9.Google Scholar
Auer, AS, Pilo, LB, Amart, PL, Wang, X, Hoffmann, D, Richards, DA, Edwards, RL, Neves, WA, Cheng, H. 2006. U-series dating and taphonomy of Quaternary vertebrates from Brazilian caves. Palaeogeography, Palaeoclimatology, Palaeoecology 240(3–4):508–22.Google Scholar
Baffa, O, Brunetti, A, Karmann, I, Neto, CMD. 2000. ESR dating of a Toxodon tooth from a Brazilian karstic cave. Applied Radiation and Isotopes 52(5):1345–9.Google Scholar
Balter, V, Saliège, J-F, Bocherenens, H, Person, A. 2002. Evidence of physico-chemical and isotopic modifications in archaeological bones during controlled acid etching. Archaeometry 44(3):329–36.Google Scholar
Barnosky, AD, Lindsey, EL. 2010. Timing of Quaternary megafaunal extinction in South America in relation to human arrival and climate change. Quaternary International 217(1–2):1029.Google Scholar
Barnosky, AD, Koch, PL, Feranec, RS, Wing, SL, Shabel, AB. 2004. Assessing the causes of Late Pleistocene extinctions on the continents. Science 306(5693):70–5.Google Scholar
Bonfim, LFC, Costa, IVG, Benvenuti, SMP. 2002. Diagnostico do municipio de Canhoba. Governo do Estado de Serdipe. Canhoba: Siperintendencia de Resursos Hidricos. 19 p.Google Scholar
Cherkinsky, A. 2009. Can we get a good radiocarbon age from “bad bone”? Determining the reliability of radiocarbon age from bioapatite. Radiocarbon 51(2):647–55.Google Scholar
Collins, MJ, Nielsen-Marsh, C, Hiller, J, Smith, CI, Roberts, JP, Prigodich, RV, Wess, TJ, Csapo, AR, Millard, AR, Turner-Walker, G. 2002. The survival of organic matter in bone: review. Archaeometry 44(3):383–94.CrossRefGoogle Scholar
Dantas, MAT, Queiroz, AN, Santos, FV, Cozzuol, MA. 2012. An anthropogenic modification in an Eremotherium tooth from North-eastern Brazil. Quaternary International 253:107–9.Google Scholar
Haas, H, Banewicz, J. 1980. Radiocarbon dating of bone apatite using thermal release of CO2 . Radiocarbon 22(2):537–44.Google Scholar
Hassan, AA, Termine, JD, Haynes, CV. 1977. Mineralogical studies on bone apatite and their application for radiocarbon dating. Radiocarbon 19(3):364–74.Google Scholar
Hedges, REM, Lee-Thorp, JA, Tuross, NC. 1995. Is tooth enamel carbonate a suitable material for radiocarbon dating? Radiocarbon 37(2):285–90.Google Scholar
Hedges, REM, Millard, AR, Pike, AWG. 1995. Measurement and relationships of diagenetic alteration of bone from three archaeological sites. Journal of Archaeological Science 22(2):201–9.Google Scholar
Koch, P, Tuross, NC, Fogel, ML. 1997. The effect of sample treatment and diagenesis on the isotopic integrity of carbonate in biogenic hydroxylapatite. Journal of Archaeological Science 24(5):417–29.Google Scholar
Martin, PS. 1984. Prehistoric overkill. The global model. In: Martin, PS, Klein, RG, editors. Quaternary Extinctions: Prehistoric Revolution. Tucson: University of Arizona Press. p 354–403.Google Scholar
Neves, W, Hubbe, A, Karmann, I. 2007. New accelerator mass spectrometry (AMS) ages suggest a revision of the electron spin resonance (ESR) Middle Holocene dates obtained for a Toxodon platensis (Toxodontidae, Mammalia) from southeast Brazil. Radiocarbon 49(3):1411–2.CrossRefGoogle Scholar
Prescott, GW, Williams, DR, Balmford, A, Green, RE, Manica, A. 2012. Quantitative global analysis of the role of climate and people in explaining late Quaternary megafaunal extinctions. Proceedings of the National Academy of Sciences of the USA 109(12):4527–31.Google Scholar
Reimer, PJ, Baillie, MGL, Bard, E, Bayliss, A, Beck, JW, Blackwell, PG, Bronk Ramsey, C, Buck, CE, Burr, GS, Edwards, RL, Friedrich, M, Grootes, PM, Guilderson, TP, Hajdas, I, Heaton, T, Hogg, AG, Hughen, KA, Kaiser, KF, Kromer, B, McCormac, FG, Manning, SW, Reimer, RW, Richards, DA, Southon, JR, Talamo, S, Turney, CSM, van der Plicht, J, Weyhenmeyer, CE. 2009. IntCal09 and Marine09 radiocarbon age calibration curves, 0–50,000 years cal BP. Radiocarbon 51(4):1111–50.Google Scholar
Rossetti, DF, de Toledo, PM, Moraes-Santos, HM, de Araújo Santos, AE Jr. 2004. Reconstruction habitats in central Amazonia using megafauna, sedimentology, radiocarbon, and isotope analyses. Quaternary Research 61(3):289–300.Google Scholar
Schoeninger, MJ, DeNiro, MJ. 1982. Carbon isotope ratios of apatite from fossil bone cannot be used to reconstruct diets of animals. Nature 297(5867):577–8.Google Scholar
Steadman, DW, Martin, PS, MacPhee, RD, Jull, AJT, McDonald, HG, Woods, CA, Iturralde-Vinent, M, Hodgins, GWL. 2005. Asynchronous extinction of late Quaternary sloths on continents and islands. Proceedings of the National Academy of Sciences of the USA 102(33):11,7638.Google Scholar
Sullivan, CH, Krueger, HW. 1981. Carbon isotope analysis of separate chemical phases in modern and fossil bone. Nature 292(5821):333–5.Google Scholar
Surovell, TA. 2000. Radiocarbon dating of bone apatite by step heating. Geoarchaeology 15(6):591–608.Google Scholar
Tamers, MA, Pearson, FG. 1965. Validity of radiocarbon dates on bone. Nature 208(5015):1053–5.Google Scholar
Tieszen, LL, Fagre, T. 1993. Effect of diet quality and composition on the isotopic composition of respiratory CO2, bone collagen, bioapatite and soft tissue. In: Lambert, J, Grupe, C, editors. Prehistoric Human Bone: Archaeology at the Molecular Level. Berlin: Springer-Verlag. p 121–55.Google Scholar
Vogel, JS, Southon, JR, Nelson, D, Brown, TA. 1984. Performance of catalytically condensed carbon for use in accelerator mass spectrometry. Nuclear Instruments and Methods in Physics Research B 5(2):289–93.CrossRefGoogle Scholar
Zazzo, A, Lécuyer, C, Mariotti, A. 2004. Experimentally-controlled carbon and oxygen isotope exchange between bioapatite inorganic and microbially-mediated conditions. Gechimica et Cosmochmica Acta 68(1):112.Google Scholar