Bioapatite is probably the key factor in the unreplicated success of vertebrates. Chemical data on bioapatite composition can be achieved on a solid sample by using different analytical tools such as spectroscopic and spectrometric methods. As analytical outputs can be affected by the physical-chemical characteristics of the sample matrix, an internal standard is usually required to correct and validate the results. Bioapatite lattice can accommodate iso- and heterovalent substitutions during life or diagenesis varying its chemical composition through (geological) time. If on the one hand, this makes bioapatite a unique archive of physical and chemical information for both the living cycle and the events occurring after death, on the other, it excludes the identification of a sole internal standard. Here, we propose a method to measure major element concentration with specific care for P, Ca, Mg, Na, K, Si, Al, and Fe, which are the main substituent atoms in bioapatite, through homemade matrix-matched external calibration standards for laser ablation inductively coupled plasma mass spectrometry (LA-ICPMS). We tested the method on living and fossil shark teeth, critically comparing the results obtained using other analytical techniques and certified external standards. We demonstrated that matrix-matched calibration in LA-ICPMS is mandatory for obtaining a reliable chemical characterization even if factors such as matrix aggregation variability, diverse presence of volatile compounds, the fossilization footprint, and the instrumental variability can represent further variability parameters.

How Much Can We Trust Major Element Quantification in Bioapatite Investigation? / Malferrari, D.; Ferretti, A.; Mascia, M. T.; Savioli, M.; Medici, L.. - In: ACS OMEGA. - ISSN 2470-1343. - 4:18(2019), pp. 17814-17822. [10.1021/acsomega.9b02426]

How Much Can We Trust Major Element Quantification in Bioapatite Investigation?

Malferrari D.
Membro del Collaboration Group
;
Ferretti A.
Membro del Collaboration Group
;
Mascia M. T.
Membro del Collaboration Group
;
Savioli M.
Membro del Collaboration Group
;
Medici L.
Membro del Collaboration Group
2019

Abstract

Bioapatite is probably the key factor in the unreplicated success of vertebrates. Chemical data on bioapatite composition can be achieved on a solid sample by using different analytical tools such as spectroscopic and spectrometric methods. As analytical outputs can be affected by the physical-chemical characteristics of the sample matrix, an internal standard is usually required to correct and validate the results. Bioapatite lattice can accommodate iso- and heterovalent substitutions during life or diagenesis varying its chemical composition through (geological) time. If on the one hand, this makes bioapatite a unique archive of physical and chemical information for both the living cycle and the events occurring after death, on the other, it excludes the identification of a sole internal standard. Here, we propose a method to measure major element concentration with specific care for P, Ca, Mg, Na, K, Si, Al, and Fe, which are the main substituent atoms in bioapatite, through homemade matrix-matched external calibration standards for laser ablation inductively coupled plasma mass spectrometry (LA-ICPMS). We tested the method on living and fossil shark teeth, critically comparing the results obtained using other analytical techniques and certified external standards. We demonstrated that matrix-matched calibration in LA-ICPMS is mandatory for obtaining a reliable chemical characterization even if factors such as matrix aggregation variability, diverse presence of volatile compounds, the fossilization footprint, and the instrumental variability can represent further variability parameters.
2019
4
18
17814
17822
How Much Can We Trust Major Element Quantification in Bioapatite Investigation? / Malferrari, D.; Ferretti, A.; Mascia, M. T.; Savioli, M.; Medici, L.. - In: ACS OMEGA. - ISSN 2470-1343. - 4:18(2019), pp. 17814-17822. [10.1021/acsomega.9b02426]
Malferrari, D.; Ferretti, A.; Mascia, M. T.; Savioli, M.; Medici, L.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11380/1199052
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