scholarly journals The combined measurement of 87Sr/86Sr isotope ratios and 88Sr/85Rb elemental ratios using laser ablation MC-ICP-MS and its application for food provenance studies: the case for Asturian beans

2018 ◽  
Vol 33 (5) ◽  
pp. 867-875 ◽  
Author(s):  
Aida Reguera-Galan ◽  
Mariella Moldovan ◽  
J. Ignacio Garcia Alonso

By combining the 87Sr/86Sr isotope ratio with the 88Sr/85Rb elemental ratio the discrimination between Asturian and South American beans was possible.

2019 ◽  
Vol 31 (2) ◽  
pp. 262-270 ◽  
Author(s):  
Lüyun Zhu ◽  
Ganglan Zhang ◽  
Yongsheng Liu ◽  
Jie Lin ◽  
Xirun Tong ◽  
...  

2018 ◽  
Vol 66 (40) ◽  
pp. 10513-10521 ◽  
Author(s):  
Agnese Aguzzoni ◽  
Michele Bassi ◽  
Peter Robatscher ◽  
Massimo Tagliavini ◽  
Werner Tirler ◽  
...  

2003 ◽  
Vol 60 (11) ◽  
pp. 1376-1385 ◽  
Author(s):  
David A Milton ◽  
Simon R Chenery

We examine 87Sr/86Sr isotope ratios in transects across the otoliths of the diadromous tropical shad hilsa, Tenualosa toli, to assess the extent of movement of fish within the large Meghna (Ganges) River system and adjacent coastal waters. Hilsa collected from marine, estuarine, and freshwater habitats were born in all main rivers in Bangladesh. All fish moved widely, entering water of marine 87Sr/86Sr isotope ratio by 1 year of age. Most returned to fresh water after they reached sexual maturity, but not necessarily to their natal region. Comparison of the 87Sr/86Sr isotope and Sr/Ca ratios of hilsa showed that in the Meghna River, 87Sr/86Sr isotope ratios can only distinguish fish from waters when the salinity was less than 5‰. Sr/Ca ratios were more useful for interpreting fish movements at higher salinities. To assess whether whole-otolith 87Sr/86Sr isotope ratios reflected the ratios of the water of natal origin, we compared the 87Sr/86Sr ratios of otolith cores with the mean 87Sr/86Sr isotope ratio of the whole transect. We found major differences between the two measurements, suggesting that 87Sr/86Sr isotope ratios from whole-otolith assays may not accurately reflect the natal origin of the fish.


Author(s):  
Anera Kazlagić ◽  
Francesco F. Russo ◽  
Jochen Vogl ◽  
Patrick Sturm ◽  
Dietmar Stephan ◽  
...  

AbstractThe 87Sr/86Sr isotope ratio can, in principle, be used for provenancing of cement. However, while commercial cements consist of multiple components, no detailed investigation into their individual 87Sr/86Sr isotope ratios or their influence on the integral 87Sr/86Sr isotope ratio of the resulting cement was conducted previously. Therefore, the present study aimed at determining and comparing the conventional 87Sr/86Sr isotope ratios of a diverse set of Portland cements and their corresponding Portland clinkers, the major component of these cements. Two approaches to remove the additives from the cements, i.e. to measure the conventional 87Sr/86Sr isotopic fingerprint of the clinker only, were tested, namely, treatment with a potassium hydroxide/sucrose solution and sieving on a 11-µm sieve. Dissolution in concentrated hydrochloric acid/nitric acid and in diluted nitric acid was employed to determine the 87Sr/86Sr isotope ratios of the cements and the individual clinkers. The aim was to find the most appropriate sample preparation procedure for cement provenancing, and the selection was realised by comparing the 87Sr/86Sr isotope ratios of differently treated cements with those of the corresponding clinkers. None of the methods to separate the clinkers from the cements proved to be satisfactory. However, it was found that the 87Sr/86Sr isotope ratios of clinker and cement generally corresponded, meaning that the latter can be used as a proxy for the clinker 87Sr/86Sr isotope ratio. Finally, the concentrated hydrochloric acid/nitric acid dissolution method was found to be the most suitable sample preparation method for the cements; it is thus recommended for 87Sr/86Sr isotope analyses for cement provenancing. Graphical abstract


2007 ◽  
Vol 390 (2) ◽  
pp. 487-494 ◽  
Author(s):  
S. Swoboda ◽  
M. Brunner ◽  
S. F. Boulyga ◽  
P. Galler ◽  
M. Horacek ◽  
...  

2016 ◽  
Vol 31 (8) ◽  
pp. 1612-1621 ◽  
Author(s):  
T. Prohaska ◽  
J. Irrgeher ◽  
A. Zitek

The simultaneous retrieval of spatially resolved information on the elemental content and isotope ratios from the same sampling spot (e.g. in incrementally grown biological material) still represents an analytical challenge.


2002 ◽  
Vol 17 (8) ◽  
pp. 887-891 ◽  
Author(s):  
Thomas Prohaska ◽  
Christopher Latkoczy ◽  
Gerald Schultheis ◽  
Maria Teschler-Nicola ◽  
Gerhard Stingeder

Author(s):  
Andreas Benjamin Kaufmann ◽  
Marina Lazarov ◽  
Stefan Kiefer ◽  
Juraj Majzlan ◽  
Stefan Weyer

Here we present a method for in-situ determination of stable antimony (Sb) isotope compositions by ultraviolet (UV)-femtosecond-laser-ablation-multi-collector-ICP-MS (fs-LA-MC-ICP-MS). Metallic antimony and a number of Sb minerals (stibnite, senarmontite, chalcostibite, tetrahedrite,...


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