The importance of mass accuracy in selected ion monitoring analysis of branched and isoprenoid tetraethers

Nina Davtian*, Edouard Bard, Guillemette Ménot, Yoann Fagault

*Corresponding author for this work

Research output: Contribution to journalArticleResearchpeer-review

11 Citations (Scopus)

Abstract

Among the new proxies based on the distribution of glycerol dialkyl glycerol tetraethers (GDGTs), the BIT index (Branched and Isoprenoid Tetraether index) is one of the most difficult to determine accurately, as shown by two round-robin GDGT studies. Sensitivity to mass spectrometer settings and tuning, and a diversity of mass spectrometry techniques may explain the relatively large observed interlaboratory scatter. However, the mass defect difference between crenarchaeol and branched GDGTs (brGDGTs) has never been specifically scrutinized. In this study, we analyzed five sediment samples with contrasting BIT values using about 60 m/z values to assess the shape of GDGT peaks using selected ion monitoring. We then assessed the biases in relative GDGT signals and mass spectrometry-derived BIT values under two scenarios which ignore the systematic mass defect difference between crenarchaeol and brGDGTs. Our results show that approximate mass selection for GDGT analysis using selected ion monitoring generates losses of relative GDGT signals of up to 36%. The observed effects on BIT values are maximal for intermediate BIT values, with shifts of BIT values of ±0.1 unit. The shifts of BIT values due to approximate mass selection are thus not negligible compared to the interlaboratory scatter evidenced by the latest round-robin GDGT study.

Original languageEnglish
Pages (from-to)58-62
Number of pages5
JournalOrganic Geochemistry
Volume118
DOIs
Publication statusPublished - Apr 2018

Keywords

  • BIT index
  • GDGTs
  • HPLC–APCI-MS
  • Mass defect difference
  • Selected ion monitoring

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