scholarly journals Prime Lab: A Dedicated AMS Facility at Purdue University

Radiocarbon ◽  
1992 ◽  
Vol 34 (3) ◽  
pp. 447-451 ◽  
Author(s):  
David Elmore ◽  
F. A. Rickey ◽  
P. C. Simms ◽  
M. E. Lipschutz ◽  
K. A. Mueller ◽  
...  

A new facility for accelerator mass spectrometry has been established at Purdue University. First results have been obtained for 10Be and 36C1, and several internal research projects have been initiated. Plans are to become a national AMS facility to serve the Earth and planetary science communities for the full range of cosmogenic radionuclides.

2002 ◽  
Vol 90 (7) ◽  
Author(s):  
E. H. Göktürk ◽  
D. J. Hillegonds ◽  
M. E. Lipschutz ◽  
I. Hodder

SummarySeveral charred plant and charcoal samples from various stratigraphic levels of the Neolithic Site, Çatalhöyük – Turkey, were dated in the AMS facility of Purdue University (PRIME Lab). Radiocarbon dates reveal a complicated chronology, as was foreseen from archeological investigations. Our measurements suggest that this unique Neolithic town may have been initiated at the East mound around 8390 BP.


2020 ◽  
Author(s):  
Alicja Wudarska ◽  
Michael Wiedenbeck ◽  
Ewa Słaby ◽  
Chris Harris ◽  
Michael M. Joachimski ◽  
...  

<p>Minerals of the apatite group, especially hydroxylapatite Ca<sub>5</sub>(PO<sub>4</sub>)<sub>3</sub>OH, are valuable archives for reconstructing environmental conditions occurring throughout the Earth’s history (e.g., Joachimski <em>et al.</em> 2009). Apatite oxygen isotope compositions have proved useful in studies of conodonts as well as fish and mammalian teeth and bones. Secondary ion mass spectrometry (SIMS) is a rapid and precise technique that enables the investigation of small and heterogeneous samples. However, this method is constrained by the availability of matrix-matched reference materials (RMs). The most commonly used RM for calibrating δ<sup>18</sup>O phosphate SIMS measurements – Durango apatite – has been found to be heterogeneous (Sun <em>et al.</em> 2016); therefore, we have undertaken this study, in which we have characterized a new suite of RMs for oxygen isotope analyses of apatite. Four potential apatite RMs obtained from various sources were assessed for <sup>18</sup>O/<sup>16</sup>O homogeneity using SIMS. The major and trace element compositions were determined by electron probe microanalyses (FE-EPMA), while the contents of OH<sup>-</sup> and CO<sub>3</sub><sup>2-</sup> were assessed using thermogravimetric analysis (TG) and infrared spectroscopy (IR). The δ<sup>18</sup>O reference values have now been determined in six independent laboratories using isotope ratio mass spectrometry (IRMS) and applying different analytical protocols, which fall into two groups: laser fluorination and high-temperature reduction of Ag<sub>3</sub>PO<sub>4</sub>. The first method provides the information on “bulk” oxygen compositions, while the second determines the composition of phosphate-bound oxygen. The repeatability of SIMS measurements on random crystal fragments was better than 0.25‰ (1 standard deviation, 1s) for the different RMs, confirming good homogeneity at the nanogram scale. The IRMS-determined δ<sup>18</sup>O<sub>SMOW</sub> values, which fall between ~5 and ~22‰ for the different samples, cover almost the full range of compositions found in igneous, metamorphic and biogenic apatite samples. However, the IRMS data collected using different techniques show offsets of ~1-2‰. The δ<sup>18</sup>O values obtained using laser fluorination are, in most cases, lower than those acquired by high-temperature reduction. Furthermore, the data collected within each group of IRMS methods reveal differences between laboratories, which do not correlate with the chemical composition of the apatite crystals. This suggests a more complex behavior of apatite during sample processing for conventional δ<sup>18</sup>O analyses as compared to other minerals such as tourmaline, and highlights the importance of the characterization of RMs with the support of multiple laboratories applying different protocols.</p><p>This research was partially funded by the Polish NCN grant no. 2013/11/B/ST10/04753 and the IGS PAS grant for the early career researchers as well as supported by the COST Action TD 1308 “ORIGINS” and the German Academic Exchange Service (DAAD).</p><p>References</p><p>Joachimski <em>et al.</em> 2009. Earth and Planetary Science Letters, 284, 599-609. doi: 10.1016/j.epsl.2009.05.028</p><p>Sun <em>et al.</em> 2016. Chemical Geology, 440, 164-178. doi: 10.1016/j.chemgeo.2016.07.013</p>


Radiocarbon ◽  
2012 ◽  
Vol 54 (3-4) ◽  
pp. 813-822 ◽  
Author(s):  
Mina Weinstein-Evron ◽  
Reuven Yeshurun ◽  
Daniel Kaufman ◽  
Eileen Eckmeier ◽  
Elisabetta Boaretto

The Natufian culture of the southern Levant played an integral role in the transition from simple huntergatherers to food-producing societies of the Neolithic, but the major Natufian hamlets are currently poorly dated. Moreover, none of these complex, continuously occupied base camps have delivered an adequate number of dates to enable an in-depth delineation of intra-Natufian developments. This paper presents the first results of our dating program at el-Wad terrace, Mount Carmel (Israel), one of the major Natufian hamlets of the “core area” of this culture. Thirteen accelerator mass spectrometry (AMS) radiocarbon age determinations were obtained from 46 bone (both ungulate and human) and charcoal samples, originating in Early Natufian living surfaces, dwellings, and burials. The obtained dates are largely in agreement with the cultural affiliation of the samples (13–15 kyr cal BP). Two series of dates from different locations show good agreement with the stratigraphy. The ages of the burials clearly point to their being younger than the living surfaces seemingly associated with them. Presently, no burials may be linked with the major architectural phase of Early Natufian el-Wad. Our ongoing dating program and the processing of additional samples from refined contexts will help shed important light on the initial phases of the Natufian culture, habitation duration, intensity, and continuity, as well as the relationships between site features and stratigraphy.


Radiocarbon ◽  
2020 ◽  
Vol 62 (5) ◽  
pp. e1-e13
Author(s):  
Rajveer Sharma ◽  
Pankaj Kumar ◽  
Sunil Ojha ◽  
Satinath Gargari ◽  
Sundeep Chopra

ABSTRACTA new facility for radiocarbon dating by accelerator mass spectrometry (AMS) was established in early 2015 at the Inter-University Accelerator Centre in New Delhi, India. The facility uses a 500 kV National Electrostatic Corporation (NEC) Pelletron accelerator for AMS measurements on graphite produced using the automated graphitization equipment (AGE) interfaced with an elemental analyzer and the carbonate handling system (CHS). A precision of better than 1‰ in the ratio of 14C/12C for the modern carbon sample and the background level of 1 × 10–15 from dead carbon sample has been achieved. This is the first dedicated accelerator of India only for AMS activities. This AMS system has the capabilities to perform 10Be and 26Al measurements as well.


Radiocarbon ◽  
2001 ◽  
Vol 43 (2A) ◽  
pp. 305-311 ◽  
Author(s):  
Darren J Hillegonds ◽  
Rae Record ◽  
Frank A Rickey ◽  
Steve Badylak ◽  
George S Jackson ◽  
...  

Processing and measurement of 200 biomedical samples has provided an opportunity to better understand the characteristics of accelerator mass spectrometry (AMS) analysis of such samples. We have utilized established procedures (Vogel 1992) and developed new methods for handling various biological samples. We have included secondary standards of known isotope ratio for all assays. A method of determining maximum precision for each unknown sample value is also reported. The presented data are an update of the ongoing radiocarbon AMS biomedical program at Purdue University.


Radiocarbon ◽  
2010 ◽  
Vol 52 (4) ◽  
pp. 1661-1666 ◽  
Author(s):  
Konrad Tudyka ◽  
Anna Pazdur ◽  
Páll Theodórsson ◽  
Adam Michczyński ◽  
Jacek Pawlyta

Liquid scintillation counting (LSC) for radiocarbon dating is a less expensive method than accelerator mass spectrometry (AMS), provides a high degree of accuracy, and is less prone to contamination due to the larger sample sizes. However, to obtain high precision, a long counting time is needed. The Gliwice Radiocarbon Laboratory is seeking to obtain an increased counting capacity with 2–3 mL benzene samples than we presently can achieve with our 2 Quantulus systems. We are therefore investigating the possibility of using a simple, single-phototube LS system (ICELS) for dating samples younger than 5000 yr. We present the first results of this investigation, including the measurement of 3 VIRI and 3 FIRI intercomparison samples.


Radiocarbon ◽  
2007 ◽  
Vol 49 (2) ◽  
pp. 339-347 ◽  
Author(s):  
Marie-Thérèse Cuzange ◽  
Emmanuelle Delqué-Količ ◽  
Tomasz Goslar ◽  
Pieter Meiert Grootes ◽  
Tom Higham ◽  
...  

We present the first results of an accelerator mass spectrometry (AMS) radiocarbon intercomparison program on 3 different charcoal samples collected in one of the hearths of the Megaceros gallery of Chauvet Cave (Ardèche, France). This cave, rich in parietal decoration, is important for the study of the appearance and evolution of prehistoric art because certain drawings have been 14C dated to the Aurignacian period at the beginning of the Upper Paleolithic. The new dates indicate an age of about 32,000 BP, which is consistent with this attribution and in agreement with the results from the same sector of the cave measured previously at the Laboratoire des Sciences du Climat et de l'Environnement (LSCE). Six laboratories were involved in the intercomparison. Samples were measured in 4 AMS facilities: Center for Isotope Research, Groningen University, the Netherlands; the Oxford Radiocarbon Accelerator Unit, UK; the Centre de datation par le carbone 14, Univ. Claude Bernard Lyon 1, France (measured by AMS facilities of Poznań University, Poland); and the LSCE, UMR CEA-CNRS-UVSQ, France (measured by the Leibniz-Labor of Christian-Albrechts-Universität Kiel, Germany).


1984 ◽  
Author(s):  
B.R. Doe ◽  
Louis Brown ◽  
David Elmore ◽  
Gregory Herzog ◽  
Theodore Kruse ◽  
...  

Radiocarbon ◽  
1997 ◽  
Vol 40 (1) ◽  
pp. 265-272 ◽  
Author(s):  
Roland Weissenbök ◽  
Steven R. Biegalski ◽  
Lloyd A. Currie ◽  
Donna B. Klinedinst ◽  
Robin Golser ◽  
...  

Accelerator mass spectrometry (AMS) at the milligram level is routinely performed, but it is difficult to go substantially below 100 μg of carbon. We discuss various approaches for sample preparation, machine operation and data evaluation, to meet the special requirements of 14C AMS measurements at the microgram-carbon level. Furthermore, we present first results obtained at the Vienna Environmental Research Accelerator (VERA) from 14C measurements of a snow sample from Gaithersburg, Maryland, USA, prepared at the National Institute of Standards and Technology (NIST).


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