Selected reviews on mass spectrometric topics. XLVII. Accelerator mass spectrometry

1992 ◽  
Vol 11 (5) ◽  
pp. 445-445 ◽  
Author(s):  
H. Budzikiewicz
Keyword(s):  
Mass Spectrometry ◽  
Accelerator Mass Spectrometry ◽  
Mass Spectrometric

Major Revisions in the Pleistocene Age Assignments for North American Human Skeletons by C-14 Accelerator Mass Spectrometry: None Older Than 11,000 C-14 Years B.P.

1985 ◽  
Vol 50 (1) ◽  
pp. 136-140 ◽  
Author(s):  
R. E. Taylor ◽  
L. A. Payen ◽  
C. A. Prior ◽  
P. J. Slota ◽  
R. Gillespie ◽  
...  
Keyword(s):  
Mass Spectrometry ◽  
North American ◽  
Accelerator Mass Spectrometry ◽  
Mass Spectrometric ◽  
Human Bone ◽  
Organic Fractions

Radiocarbon analyses by accelerator mass spectrometric (AMS) techniques on organic fractions of human bone from various North American localities previously assigned ages ranging from about 70,000 to 15,000 years B.P. now suggest that none of these skeletons is older than 11,000 C-14 years B.P.

Fundamentals of accelerator mass spectrometry

1987 ◽  
Vol 323 (1569) ◽  
pp. 5-21 ◽  
Keyword(s):  
Mass Spectrometry ◽  
Accelerator Mass Spectrometry ◽  
High Sensitivity ◽  
Isotope Ratios ◽  
Mass Spectrometric ◽  
Negative Ion ◽  
Significant Extension ◽  
Mass Spectrometric Techniques

The extension of high-sensitivity mass spectrometry to isotope ratios in the range 10 -12 - 10 -15 has been called accelerator mass spectrometry (AMS) because of the use of an additional stage of acceleration that facilitates the removal of molecular interferences and the separation of isobars. In some cases the ultra-high sensitivity is obtained by exploiting the instability of the negative ion of the interfering isobar. It is now possible to measure such isotopes as 14 C at natural abundances as low as one atom in 10 +15 12 C atoms. The ideas behind this significant extension of mass spectrometric techniques will be discussed.

Confounding contaminants in mass spectrometric reaction monitoring

2018 ◽  
Author(s):  
Gilian T. Thomas ◽  
Landon MacGillivray ◽  
Natalie L. Dean ◽  
Rhonda L. Stoddard ◽  
Lars Yunker ◽  
...  
Keyword(s):  
Mass Spectrometry ◽  
Mass Spectrometric ◽  
Negative Ion ◽  
Reaction Monitoring ◽  
Schlenk Flask ◽  
Dynamic Analyses ◽  
Rubber Septa ◽  
Negative Ion Mode ◽  
Mode A

<p>Reactions carried out in the presence of rubber septa run the risk of additives being leached out by the solvent. Normally, such species are present at low enough levels that they do not interfere with the reaction significantly. However, when studying reactions using sensitive methods such as mass spectrometry, the appearance of even trace amounts of material can confuse dynamic analyses of reactions. A wide variety of additives are present in rubber along with the polymer: antioxidants, dyes, detergent, and vulcanization agents, and these are all especially problematic in negative ion mode. A redesigned Schlenk flask for pressurized sample infusion (PSI) is presented as a means of practically eliminating the presence of contaminants during reaction analyses.</p>

scholarly journals Hiatus in Prehistoric Chronology of the Cis-Baikal Region, Siberia: Pattern or Artifact?

Radiocarbon ◽  
2007 ◽  
Vol 49 (1) ◽  
pp. 123-129 ◽  
Author(s):  
Yaroslav V Kuzmin
Keyword(s):  
Mass Spectrometry ◽  
Accelerator Mass Spectrometry ◽  
Baikal Region ◽  
Critical Evaluation ◽  
Burial Grounds

The problem of a hiatus at about 6100–5300 BP (about 4900–4200 cal BC) in the prehistoric chronology of the Cis-Baikal region in Siberia is discussed. Based on a critical evaluation of existing evidence, there was no discontinuity found in the cultural sequence between the Kitoi and Serovo/Glazkovo complexes of the Neolithic, and the proposed “hiatus” may be an artifact based on underestimation of solid data. Conventional 14C dates are presented that were generated in the 1980s to early 2000s for Cis-Baikal prehistoric burial grounds, and were later dated by the accelerator mass spectrometry (AMS).

Resolution of a protein sequence ambiguity by X-ray crystallographic and mass spectrometric methods

1992 ◽  
Vol 25 (2) ◽  
pp. 205-210 ◽  
Author(s):  
L. J. Keefe ◽  
E. E. Lattman ◽  
C. Wolkow ◽  
A. Woods ◽  
M. Chevrier ◽  
...  
Keyword(s):  
Mass Spectrometry ◽  
Amino Acid ◽  
Electron Density ◽  
Mass Spectrometric ◽  
Amino Acid Sequences ◽  
Data Matrix ◽  
Protein Crystal ◽  
Insertion Mutant ◽  
Laser Desorption Mass Spectrometry ◽  
X Ray

Ambiguities in amino acid sequences are a potential problem in X-ray crystallographic studies of proteins. Amino acid side chains often cannot be reliably identified from the electron density. Many protein crystal structures that are now being solved are simple variants of a known wild-type structure. Thus, cloning artifacts or other untoward events can readily lead to cases in which the proposed sequence is not correct. An example is presented showing that mass spectrometry provides an excellent tool for analyzing suspected errors. The X-ray crystal structure of an insertion mutant of Staphylococcal nuclease has been solved to 1.67 Å resolution and refined to a crystallographic R value of 0.170 [Keefe & Lattman (1992). In preparation]. A single residue has been inserted in the C-terminal α helix. The inserted amino acid was believed to be an alanine residue, but the final electron density maps strongly indicated that a glycine had been inserted instead. To confirm the observations from the X-ray data, matrix-assisted laser desorption mass spectrometry was employed to verify the glycine insertion. This mass spectrometric technique has sufficient mass accuracy to detect the methyl group that distinguishes glycine from alanine and can be extended to the more common situation in which crystallographic measurements suggest a problem with the sequence, but cannot pinpoint its location or nature.

scholarly journals 14C INTERCOMPARISON EXERCISE ON BONES AND IVORY SAMPLES: IMPLICATIONS FOR FORENSICS

Radiocarbon ◽  
2021 ◽  
pp. 1-12
Author(s):  
G Quarta ◽  
M Molnár ◽  
I Hajdas ◽  
L Calcagnile ◽  
I Major ◽  
...  
Keyword(s):  
Mass Spectrometry ◽  
International Atomic Energy Agency ◽  
Accelerator Mass Spectrometry ◽  
Reference Curve ◽  
Nuclear Testing ◽  
Energy Agency ◽  
Widespread Application ◽  
Intercomparison Exercise ◽  
High Degree ◽  
Data Calibration

ABSTRACT The application of accelerator mass spectrometry radiocarbon (AMS 14C) dating in forensics is made possible by the use of the large excursion of the 14C concentration in the post-WWII terrestrial atmosphere due to nuclear testing as a reference curve for data calibration. By this approach high-precision analyses are possible on samples younger than ∼70 years. Nevertheless, the routine, widespread application of the method in the practice of forensics still appears to be limited by different issues due to possible complex interpretation of the results. We present the results of an intercomparison exercise carried out in the framework of an International Atomic Energy Agency (IAEA) CRP-Coordinated Research Project between three AMS laboratories in Italy, Hungary, and Switzerland. Bone and ivory samples were selected with ages spanning from background (>50 ka) to 2018. The results obtained allow us to assess the high degree of reproducibility of the results and the remarkable consistency of the experimental determinations.

Vitamin D analyses in veterinary feeds by gas chromatography-tandem mass spectrometry

2021 ◽  
pp. 146906672110002
Author(s):  
Andreas Lehner ◽  
Margaret Johnson ◽  
Alan Zimmerman ◽  
Justin Zyskowski ◽  
John Buchweitz
Keyword(s):  
Mass Spectrometry ◽  
Vitamin D ◽  
Gas Chromatography ◽  
Liquid Chromatography ◽  
Tandem Mass Spectrometry ◽  
Vitamin D3 ◽  
Mass Spectrometric ◽  
Chromatographic Behavior ◽  
Tandem Mass ◽  
Chromatography Tandem Mass Spectrometry

This report examines the feasibility of determination of Vitamin D3, D2 and their 25-hydroxy metabolites utilizing Gas Chromatography Tandem Mass Spectrometry (GC/MS/MS) as a potential alternative to popular Liquid Chromatography Tandem Mass Spectrometric (LC/MS/MS) methodologies. The GC/MS/MS approach was found to operate reasonably well despite long-standing concerns that gas-liquid chromatography of vitamin D compounds invoke thermal rearrangements owing to the relatively high inlet and capillary column temperatures used. The workup procedure involved incubation of feed samples with concentrated potassium hydroxide for overnight fat saponification, extraction of D Vitamins in n-hexane and reaction with N,O-bis(trimethylsilyl)trifluoroacetamide at 70 °C for 30 mins. In addition to parent compounds, small amounts of pyro-, isopyro-, and iso-vitamin D and isotachysterol3 variants were obtained from each Vitamin D-related compound upon extraction and GC/MS/MS analysis. Mass spectral and chromatographic behavior of these compounds are herein described and interpreted. Multiple Reaction Monitoring settings on GC/MS/MS included m/z 456→351 for Vitamin D3 and m/z 486→363 for Vitamin D2. Trimethylsilylation enabled single predominant peaks for Vitamins D3 and D2, and sample workup in the presence of deuterated Vitamin D analogs enabled accurate and precise sensitivity to 1 ppb (ng/g) in feeds. The method could be extended with reasonable accuracy to 25-hydroxy (25OH) compounds, but accuracies would be significantly improved by inclusion of respective 25OH-specific deuterated internal standards. The method was applied to 27 submissions of suspect dog foods of which 22% were discovered elevated and 44% were discovered to contain toxic levels of Vitamin D3. The described method was thus discovered to provide a suitable mass spectrometric approach for Vitamin D, proving itself here specifically of value in detection of ergocalciferol and cholecalciferol in animal feeds. The specificity and sensitivity of the tandem quadrupole approach can enable suitable applicability to serum determination if desired.

scholarly journals Dating of Cremated Bones

Radiocarbon ◽  
2001 ◽  
Vol 43 (2A) ◽  
pp. 249-254 ◽  
Author(s):  
J N Lanting ◽  
A T Aerts-Bijma ◽  
J van der Plicht
Keyword(s):  
Mass Spectrometry ◽  
Success Rate ◽  
Accelerator Mass Spectrometry ◽  
Bone Collagen ◽  
Organic Fraction ◽  
Mineral Fraction

When dating unburnt bone, bone collagen, the organic fraction of the bone, is used. Collagen does not survive the heat of the cremation pyre, so dating of cremated bone has been considered impossible. Structural carbonate in the mineral fraction of the bone, however, survives the cremation process. We developed a method of dating cremated bone by accelerator mass spectrometry (AMS), using this carbonate fraction. Here we present results for a variety of prehistoric sites and ages, showing a remarkable success rate for this method.

scholarly journals THE BEGINNING OF THE IRON AGE AT ARSLANTEPE: A 14C PERSPECTIVE

Radiocarbon ◽  
2021 ◽  
pp. 1-19
Author(s):  
Federico Manuelli ◽  
Cristiano Vignola ◽  
Fabio Marzaioli ◽  
Isabella Passariello ◽  
Filippo Terrasi
Keyword(s):  
Mass Spectrometry ◽  
Bronze Age ◽  
High Precision ◽  
Iron Age ◽  
Accelerator Mass Spectrometry ◽  
Late Bronze Age ◽  
13Th Century ◽  
Historical Events ◽  
Preliminary Results ◽  
Archaeological Data

ABSTRACT The Iron Age chronology at Arslantepe is the result of the interpretation of Luwian hieroglyphic inscriptions and archaeological data coming from the site and its surrounding region. A new round of investigations of the Iron Age levels has been conducted at the site over the last 10 years. Preliminary results allowed the combination of the archaeological sequence with the historical events that extended from the collapse of the Late Bronze Age empires to the formation and development of the new Iron Age kingdoms. The integration into this picture of a new set of radiocarbon (14C) dates is aimed at establishing a more solid local chronology. High precision 14C dating by accelerator mass spectrometry (AMS) and its correlation with archaeobotanical analysis and stratigraphic data are presented here with the purpose of improving our knowledge of the site’s history and to build a reliable absolute chronology of the Iron Age. The results show that the earliest level of the sequence dates to ca. the mid-13th century BC, implying that the site started developing a new set of relationships with the Levant already before the breakdown of the Hittite empire, entailing important historical implications for the Syro-Anatolian region at the end of the 2nd millennium BC.

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