AN ASSESSMENT OF BACK-SCATTERED ELECTRON PETROGRAPHY AS A METHOD FOR DISTINGUISHING MEDITERRANEAN OBSIDIANS

The recent application by Burton and Krinsley (1987) of back-scattered electron (BSE) petrography to obsidians from sources located in the south-western United States established that this method can effectively resolve and characterize included micro-crystalline phases that have proven difficult to analyse by optical thin-section microscopy. In the first extension of their original study, we have examined, using BSE petrography, obsidians from island sources located in the Mediterranean, including sources known to have been exploited in prehistory. Because of the kinetic contrasts on their crystallization, these microcrystalline phases reflect the magmatic history of the obsidian, providing information about superheating, supercooling, sub-solidus processes, and other phenomena. This information is of significance for the chemical analysis of Mediterranean obsidians and also as the basis for a powerful alternative to existing non-destructive analytical methods for the sourcing of archaeological and art-historical obsidian.     

Isothermal Time‐Series Determination of the Rate of Diffusion of Water in Pachuca Obsidian*

Friedman and Smith's (1960) article introducing an exciting, potentially precise and inexpensive method of dating obsidian artefacts has thus far failed to reach its potential. Numerous efforts to refine, improve and even redevelop the method since that time have similarly failed to achieve the original promise. Only within the last eight years have significant improvements been made, due to both improved analytical techniques and a better understanding of the hydration process. However, most of our mechanistic understanding of the interaction of water with rhyolitic glass is based on experiments performed on melts and glasses at temperatures above their glass transitions, conditions inappropriate for investigation of near‐surface environmental conditions. Unfortunately, studies detailing the temporal evolution of the diffusion profile at low temperatures are rare, and few useful data are available on the low‐temperature diffusive hydration of silicate glasses. This paper presents data on the experimental hydration of obsidian from the Pachuca source (a.k.a. Sierra de las Navajas, Basin of Mexico) at 75°C for times ranging from 3 to 562 days, and compares these results with data for samples obtained from a stratigraphic excavation of the Chalco site in the Basin of Mexico. Samples have been analysed using secondary ion mass spectrometry (SIMS) to provide concentration/depth data. While 75°C is still significantly above the temperatures at which archaeological obsidians hydrate, it is well below the glass transition temperature (approx. 400°C) and thus processes are likely to be similar to those that occur in nature, but fast enough to be observed over a laboratory timescale. The results demonstrate that a simple square‐root‐of‐time model of the evolution of the diffusion profile is not adequate to describe the diffusion process, as measured diffusion profiles exhibit the effects of concentration‐ and time‐dependent, non‐Fickian diffusion. With progressive hydration, characteristic diffusion coefficients first decrease, then increase with time. Surface concentration increases with time, but an intermediate plateau is observed in its time evolution that is consistent with results obtained from the suite of Chalco samples. Both of these effects have been observed during diffusion in glassy polymer systems and are associated with the build‐up and relaxation of self‐stress caused by the influx of diffusing material.     

PROVENANCE STUDIES OF CHALCOLITHIC OBSIDIAN ARTEFACTS FROM NEAR LAKE URMIA, NORTHWESTERN IRAN USING WDXRF ANALYSIS

In 2005–2006 we initiated a major archaeological survey and chemical characterization study to investigate the long-term use of obsidian along the eastern shores of Lake Urmia, northwestern Iran. Previous research in the area suggested that almost all archaeological obsidian found in this area originated from the Nemrut Daĝ source located in the Lake Van region of Anatolia (Turkey). More recent research on obsidian artefacts from the Lake Urmia region has identified a significant number of obsidian artefacts with compositions different from the sources near Lake Van. This suggests that the obsidian artefacts are from a yet to be identified geological source, but possibly one that was not too distant. In order to advance our knowledge of Iranian obsidians and eventually refine provenance criteria we analysed obsidian from 22 Chalcolithic sites and some source areas. The compositions of both obsidian source samples and artefacts were determined using wave length dispersive X-ray fluorescence spectrometry (WDXRF). This paper presents results from the trace elemental analysis of both geological and archaeological obsidians, providing important new data concerning the diachronic relationship between lithic technology and raw material in the north-west of Iran.     

NON‐DESTRUCTIVE SOURCING OF BRONZE AGE NEAR EASTERN OBSIDIAN ARTEFACTS: REDEVELOPING AND REASSESSING ELECTRON MICROPROBE ANALYSIS FOR OBSIDIAN SOURCING*

Despite predictions in the 1980s that electron microprobe analysis (EMPA) would become a popular technique for obsidian sourcing, few studies have used it with this goal, and most of them are now outdated and unrepresentative of modern EMPA. For example, Merrick and Brown (1984 ) recorded their data on punch cards. Furthermore, these studies destructively prepared artefacts for analysis. The research at hand endeavoured: (1) to establish the modern capabilities of EMPA for obsidian sourcing; and (2) to develop and evaluate procedures for non‐destructive artefact analysis. Issues such as diagenetic effects and compatibility with NAA and XRF data were also investigated.     

THE PROVENANCE OF OBSIDIAN ARTEFACTS FROM THE WĀDĪ ATH‐THAYYILAH 3 NEOLITHIC SITE (EASTERN YEMEN PLATEAU) BY LA–ICP–MS

The geological sources of obsidian in the Red Sea region provide the raw material used for the production of obsidian artefacts found in prehistoric sites on both sides of the Red Sea, as far afield as Egypt, the Persian Gulf and Mesopotamia. This paper presents the chemical characterization of five obsidian geological samples and 20 prehistoric artefacts from a systematically excavated Neolithic settlement in highland Yemen. The major element concentrations were determined by SEM–EDS analysis and the trace element concentrations were analysed by the LA–ICP–MS method, an almost non‐destructive technique capable of chemically characterizing the volcanic glass. A comparison of archaeological and geological determinations allows the provenance of the obsidian used for the Neolithic artefacts to be traced to definite sources in the volcanic district of the central Yemen Plateau.     

NO STONE UNBURNED: A COMPOSITIONAL ANALYSIS OF OBSIDIAN MICRODEBITAGE BY LASER ABLATION TOF–ICP–MS

Obsidian is an effective material for the study of prehistoric raw material use and exchange, due to the high degree of homogeneity and redundancy of obsidian materials and manufactured objects in the archaeological record. The destructive nature of many analytical techniques often impedes compositional research because of the damage that may occur to priceless archaeological artefacts. The combination of time‐of‐flight (TOF) ICP–MS with a laser ablation sample introduction system provides a highly efficient means of chemically characterizing obsidian. This study shows that sample size limit capabilities of TOF–ICP–MS analysis of obsidian can reach less than 100 μm. Sampling and analysis of microartefacts enables researchers to overcome problems of sampling bias with very little damage to the valuable existing materials within the archaeological record and expands the potential for chemical compositional analyses in archaeology.     

AN ASSESSMENT OF THE CURRENT APPLICATIONS AND FUTURE DIRECTIONS OF OBSIDIAN SOURCING STUDIES IN ARCHAEOLOGICAL RESEARCH*

This paper thematically characterizes a large body of recent obsidian sourcing discourse as a means of highlighting the current place of obsidian provenance studies in larger archaeological discourse. It is shown that the field of obsidian sourcing is flourishing, with a clear upward trend in the number of published studies in the past decade. This paper further argues that sourcing is a means to an end, a way to determine where artefacts originate, and thus a means of addressing broader archaeological problems. Through this contextual framework, obsidian sourcing studies—and indeed all provenance studies—are seen as relevant because they transcend the increasingly specialized world of archaeological discourse.     

Melian obsidian in NW Turkey: Evidence for early Neolithic trade

Abstract

Archaeological investigations carried out at the Early Neolithic coastal site of Co?kuntepe in northwestern Turkey yielded an assemblage of 110 obsidian artifacts displaying the macroscopic characteristics of the well-known obsidian deposits on the Cycladic island of Melos. Analysis of three samples from this homogeneous obsidian assemblage using both X-Ray Fluorescence and Laser Ablation High Resolution Inductively Coupled Plasma Mass Spectrometry confirmed that these artifacts were derived from Melos. The presence of these Melian obsidian artifacts at Co?kuntepe, along with a few pieces with central Anatolian macroscopic characteristics, is intriguing because intensive production of tools made of local flint was also identified at the site through the analysis of surface scatters. This finding raises the question of the status of obsidian and associated procurement systems. The presence of obsidian can be also used to argue that certain coastal villages acted as nodes of exchange for Aegean seafarers at times in the late 7th millennium B.C.     

PARTICLE‐INDUCED X‐RAY EMISSION (PIXE) ANALYSIS OF OBSIDIAN FROM TEOTIHUACAN

A collection of 50 archaeological obsidian samples studied in the framework of the Preciudadela Project (Teotihuacan, Mexico) has been analysed using particle‐induced X‐ray emission (PIXE) with the external beam line of the Accélérateur Grand Louvre d'Analyse Elémentaire facility (C2RMF, Paris) and of the Instituto de Física (UNAM, Mexico). This work addresses the provenance of these obsidian samples, with the purpose of determining if they come from the obsidian sources exploited by Teotihuacans (mainly Otumba and Sierra de Pachuca), from other sources, or arrived via commercial exchanges with other regions. For that, the elemental compositions derived from the PIXE spectra have been compared with data published in the literature on the basis of instrumental neutron activation analysis. From the concentrations of selected key elements (Na, K, Mn, Fe, Zn, Rb, Sr, Zr), it was possible to unambiguously assign the provenance of most samples. Many originate from two major sources, namely Sierra de Pachuca (Hidalgo) and Otumba (Mexico), which were the main obsidian deposits used by the Teotihuacans. However, some samples exhibit a compositional fingerprint matching other provenances, i.e., Paredón (Puebla) and Zacualtipan (Hidalgo).     

MECHANICAL PROPERTIES OF STONE ARTEFACT MATERIALS AND THE EFFECT OF HEAT TREATMENT*

Mechanical testing of lithologies used for stone tool manufacture has shown that fracture toughness is the most objective measure of the quality of raw materials shaped by either flaking or pecking/grinding. Materials amenable to pressure flaking and blade manufacture have low values of fracture toughness, whereas those shaped by pecking/grinding have high values. The fracture toughness test is also the most definitive for quantifying the improvement in flaking properties of materials subjected to intentional heat treatment. Cryptocrystalline and macrocrystalline siliceous lithologies demonstrate a well-defined, gradual reduction in fracture toughness with increased temperature. When heated to optimum temperatures, their fracture toughness approaches that of obsidian, the lithology generally regarded as having the best flaking properties.