Santander, February 19th-22nd 2008 - Aranzadi
Santander, February 19th-22nd 2008 - Aranzadi
Santander, February 19th-22nd 2008 - Aranzadi
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20<br />
KATERINA DOUKA, THOMAS F. G. HIGHAM AND ROBERT E. M. HEDGES<br />
rred substrates and food selection are generally wellstudied,<br />
hence, retrieval of this type of material from an<br />
archaeological site offers important local habitat and<br />
environmental information as well as insights into several<br />
behavioural features of the linked human community<br />
(e.g. exploitation of shellfish for food, for use in the<br />
production of tools or weapons, or utilization for<br />
symbolic reasons).<br />
As dating material, molluscs offer both relative and<br />
absolute chronometric information.<br />
Seasonality studies fall into the former category.<br />
Relative growth-ring and oxygen isotope measurements<br />
provide information regarding the age-at-death<br />
of shellfish within archaeological sites, and enable a<br />
seasonal signal to be diagnosed (e.g. Koike 1973,<br />
1979, Deith 1983, Deith 1985, 1986, Milner 2001,<br />
Dupont 2006). This is critical information for the construction<br />
of seasonal subsistence patterns and the<br />
movement of people within specific regions in the past.<br />
Absolute methods such as Radiocarbon ( 14 C)<br />
dating, Amino Acid Racemisation (AAR), Uraniumseries<br />
and Electron Spin Resonance (ESR), can be all<br />
used for the direct dating of molluscan remains, allowing<br />
secure inter and intra-site correlations when<br />
humans are responsible for their accumulation (e.g.<br />
Kaufman 1971, Wehmiller 1984, Skinner 1988;<br />
Bezzera et al 2000, Penkman et al. <strong>2008</strong>).<br />
This paper specifically deals with 14 C dating and<br />
reviews the basis of the method in so far as it is used to<br />
date marine and estuarine shell carbonates. It will discuss<br />
the fundamental assumptions, related uncertainties<br />
and problems, along with new developments and<br />
their application to a significant problem of the European<br />
prehistory, the Middle to Upper Palaeolithic transition.<br />
2. FUNDAMENTALS ON MARINE SHELLS<br />
Molluscan skeletons are polycrystalline biominerals<br />
mainly composed of calcium carbonate<br />
(CaCO3) precipitated as distinct layers within an<br />
organic proteinaceous matrix. In marine shells<br />
CaCO3 comprises high-Mg calcite and aragonite, in<br />
several formations.<br />
The two polymorphs, aragonite and calcite,<br />
share identical chemical compositions but quite different<br />
crystal structures and thermodynamic equilibria,<br />
with calcite being the stable form and aragonite<br />
the metastable form at present earth-surface temperatures<br />
and pressures.<br />
Carbon (C) is one of the main elements<br />
molluscs make use of to form their exoskeletons.<br />
The origin of this carbon derives from various sources<br />
and the mixing of different carbon pools leads<br />
to their isotopic deviation from the ambient environment.<br />
Shells incorporate carbon deriving from<br />
two pools: oceanic dissolved inorganic carbon<br />
(DIC) and carbon from respiratory CO2 mainly<br />
stemming from food metabolism (Tanaka et al.<br />
1986, McConnaughey et al. 1997, Gillikin et al.<br />
2007). For a full summary on the current status of<br />
research regarding the C isotopes of biological<br />
carbonates the reader is referred to recent publication<br />
by McConnaughey and Gillikin (<strong>2008</strong>) and<br />
references therein.<br />
3. RADIOCARBON DATING OF SHELLS<br />
Radiocarbon dating is the most commonly used<br />
chronometric technique in archaeology. Carbon (C)<br />
is found in the atmosphere in the form of three isotopes<br />
1 12 C, 13 C and 14 C, which account for the element’s<br />
natural abundance. The first two, 12 C and 13 C,<br />
are stable isotopes and can be found in atmospheric<br />
concentrations of approximately 98.89% and<br />
1.11% respectively, whereas 14 C is weakly radioactive<br />
and has an extremely low atmospheric activity, of<br />
about one per trillion 12 C atoms.<br />
Radiocarbon is produced in the stratosphere<br />
and shortly after is oxidized to 14 CO2. It rapidly<br />
enters circulation and exchanges with the oceans<br />
and biosphere (Fairbanks et al. 2005, Bronk<br />
Ramsey <strong>2008</strong>). Each living organism will incorporate<br />
14 C atoms through photosynthetic, respiratory,<br />
metabolic, and other biological pathways and will<br />
reach isotopic equilibrium with the ambient environment.<br />
This ceases to exist when the organism<br />
dies. 14 C is no longer incorporated into its tissues,<br />
and the radioactive 14 C isotope undergoes nuclear<br />
decay. The decay progresses exponentially at<br />
a regular rate expressed as the constant known<br />
as the radiocarbon half-life, often quoted to be<br />
5730 2 years.<br />
1<br />
Isotopes are varieties of the same element, which contain the same number of electrons and protons (same atomic number) but different<br />
number of neutrons (hence different mass number) in their nuclei. Most elements are found in mixtures of two or more, stable and unstable<br />
(radioactive) isotopes. Variations in isotope abundance of an element are caused either by radioactive decay of the unstable isotopes or by<br />
isotope fractionation (Hoefs 2003: 1–5).<br />
2<br />
Two values are often quoted for the rate of 14 C decay. The first to be published was the Libby half-life 5568 ± 30 years (Anderson and Libby<br />
1951) and the second is the Cambridge half-life of 5730 ± 40 years (Godwin 1962), often thought to be more accurate. However, very recently<br />
(Fairbanks et al. 2005) supported the idea that the half-life may be significantly different, as much as 6000 years, although this idea is not<br />
widely accepted (see for example, Roberts and Southon 2007).<br />
MUNIBE Suplemento - Gehigarria 31, 2010<br />
S.C. <strong>Aranzadi</strong>. Z.E. Donostia/San Sebastián