Carbonate clumped isotope analyses with the long‐integration dual‐inlet (LIDI) workflow: scratching at the lower sample weight boundaries. (21st May 2017)
- Record Type:
- Journal Article
- Title:
- Carbonate clumped isotope analyses with the long‐integration dual‐inlet (LIDI) workflow: scratching at the lower sample weight boundaries. (21st May 2017)
- Main Title:
- Carbonate clumped isotope analyses with the long‐integration dual‐inlet (LIDI) workflow: scratching at the lower sample weight boundaries
- Authors:
- Müller, Inigo A.
Fernandez, Alvaro
Radke, Jens
van Dijk, Joep
Bowen, Devon
Schwieters, Johannes
Bernasconi, Stefano M. - Abstract:
- Abstract : Rationale: Clumped isotope analyses ( Δ 47 ) of carbonates by dual inlet (DI) mass spectrometry require long integration times to reach the necessary high precision due to the low abundance of the rare isotopologue 13 C 18 O 16 O. Traditional DI protocols reach this only with large amounts of sample and/or a large number of replicates as a large portion of the analyte gas is wasted. We tested an improved analytical workflow that significantly reduces the sample sizes and total analysis time per sample while preserving precision and accuracy. Methods: We implemented the LIDI (long‐integration dual‐inlet) protocol to measure carbonates in micro‐volume mode using a Kiel IV carbonate device coupled to a Thermo Scientific 253 Plus isotope ratio mass spectrometer without the new 10 13 ohm amplifier technology. The LIDI protocol includes a single measurement of the sample gas (600 s integration) followed by a single measurement of the working gas (WG) with the same integration time. Results: The Δ 47 measurements of four calcite standards over a period of 5 weeks demonstrate excellent long‐term stability with a standard deviation of ±0.021 to ±0.025 ‰ for the final values of the individual aliquots. The Δ 47 analyses of a coral, four foraminifera and a calcite precipitated in the laboratory demonstrate that 14 replicates of 90 to 120 μg are sufficient to achieve an external precision of ±0.007 ‰ (1SE) or of ±0.013 ‰ at the 95% confidence level. Conclusions: This studyAbstract : Rationale: Clumped isotope analyses ( Δ 47 ) of carbonates by dual inlet (DI) mass spectrometry require long integration times to reach the necessary high precision due to the low abundance of the rare isotopologue 13 C 18 O 16 O. Traditional DI protocols reach this only with large amounts of sample and/or a large number of replicates as a large portion of the analyte gas is wasted. We tested an improved analytical workflow that significantly reduces the sample sizes and total analysis time per sample while preserving precision and accuracy. Methods: We implemented the LIDI (long‐integration dual‐inlet) protocol to measure carbonates in micro‐volume mode using a Kiel IV carbonate device coupled to a Thermo Scientific 253 Plus isotope ratio mass spectrometer without the new 10 13 ohm amplifier technology. The LIDI protocol includes a single measurement of the sample gas (600 s integration) followed by a single measurement of the working gas (WG) with the same integration time. Results: The Δ 47 measurements of four calcite standards over a period of 5 weeks demonstrate excellent long‐term stability with a standard deviation of ±0.021 to ±0.025 ‰ for the final values of the individual aliquots. The Δ 47 analyses of a coral, four foraminifera and a calcite precipitated in the laboratory demonstrate that 14 replicates of 90 to 120 μg are sufficient to achieve an external precision of ±0.007 ‰ (1SE) or of ±0.013 ‰ at the 95% confidence level. Conclusions: This study demonstrates that by using a Kiel IV–253 Plus system with LIDI it is possible to achieve the same analytical precision as conventional DI measurements with at least a factor of 40 less sample material. With the new 10 13 ohm resistor technology there is the potential to reduce the required sample material even more. This opens new avenues of research in paleoceanography, paleoclimatology, low‐temperature diagenesis and other currently sample size limited applications. Copyright © 2017 John Wiley & Sons, Ltd. … (more)
- Is Part Of:
- Rapid communications in mass spectrometry. Volume 31:Number 12(2017)
- Journal:
- Rapid communications in mass spectrometry
- Issue:
- Volume 31:Number 12(2017)
- Issue Display:
- Volume 31, Issue 12 (2017)
- Year:
- 2017
- Volume:
- 31
- Issue:
- 12
- Issue Sort Value:
- 2017-0031-0012-0000
- Page Start:
- 1057
- Page End:
- 1066
- Publication Date:
- 2017-05-21
- Subjects:
- Mass spectrometry -- Periodicals
543.65 - Journal URLs:
- http://onlinelibrary.wiley.com/ ↗
- DOI:
- 10.1002/rcm.7878 ↗
- Languages:
- English
- ISSNs:
- 0951-4198
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 7254.440000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
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