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Accurate measurement of K/Ca in low‐[K] carbonate samples using laser‐ablation sector‐field inductively coupled plasma mass spectrometry

Accurate measurement of K/Ca in low‐[K] carbonate samples using laser‐ablation sector‐field inductively coupled plasma mass spectrometry
Accurate measurement of K/Ca in low‐[K] carbonate samples using laser‐ablation sector‐field inductively coupled plasma mass spectrometry
Rationale: potassium (K) is a major component of several silicate minerals and seawater, and, therefore, constraining past changes in the potassium cycle is a promising way of tracing large-scale geological processes on Earth. However, [K] measurement using inductively coupled plasma mass spectrometry (ICP-MS) is challenging due to an ArH+ interference, which may be of a similar magnitude to the K+ ion beam in samples with <0.1% m/m [K].

Methods: in this work, we investigated the effect of the ArH+ interference on K/Ca data quality by comparing results from laser-ablation (LA)-ICP-MS measured in medium and high mass resolution modes and validating our LA results via solution ICP-optical emission spectroscopy (OES) and solution ICP-MS measurements. To do so, we used a wide range of geological reference materials, with a particular focus on marine carbonates, which are potential archives of past changes in the K cycle but are typically characterised by [K] < 200 μg/g. In addition, we examine the degree to which trace-element data quality is driven by downhole fractionation during LA-ICP-MS measurements.

Results: our results show that medium mass resolution (MR) mode is sufficiently capable of minimising the effect of the ArH+ interference on K+. However, the rate of downhole fractionation for Na and K varies between different samples as a result of their differing bulk composition, resulting in matrix-specific inaccuracy. We show how this can be accounted for via downhole fractionation corrections, resulting in an accuracy of better than 1% and a long-term reproducibility (intermediate precision) of <6% (relative standard deviation) in JCp-1NP using LA-ICP-MS in MR mode.

Conclusion: our [K] measurement protocol is demonstrably precise and accurate and applicable to a wide range of materials. The measurement of K/Ca in relatively low-[K] marine carbonates is presented here as a key example of a new application opened up by these advances.
0951-4198
Nambiar, Romi
072685f3-79ae-46b9-b7b7-0de4b574d7f9
Kniest, Jorit F.
eb0b180d-ec5e-4051-b602-36c19bc74b09
Schmidt, Alexander
364b69e1-ac6c-4528-979c-861419bb16ec
Raddatz, Jacek
c8083ba7-cd49-4017-9119-9ef32a3d8435
Müller, Wolfgang
360a71f7-0b47-4ff3-8c32-1912d70401aa
Evans, David
878c65c7-eab9-4362-896b-166e165eb94b
Nambiar, Romi
072685f3-79ae-46b9-b7b7-0de4b574d7f9
Kniest, Jorit F.
eb0b180d-ec5e-4051-b602-36c19bc74b09
Schmidt, Alexander
364b69e1-ac6c-4528-979c-861419bb16ec
Raddatz, Jacek
c8083ba7-cd49-4017-9119-9ef32a3d8435
Müller, Wolfgang
360a71f7-0b47-4ff3-8c32-1912d70401aa
Evans, David
878c65c7-eab9-4362-896b-166e165eb94b

Nambiar, Romi, Kniest, Jorit F., Schmidt, Alexander, Raddatz, Jacek, Müller, Wolfgang and Evans, David (2024) Accurate measurement of K/Ca in low‐[K] carbonate samples using laser‐ablation sector‐field inductively coupled plasma mass spectrometry. Rapid Communications in Mass Spectrometry, 38 (5), [e9692]. (doi:10.1002/rcm.9692).

Record type: Article

Abstract

Rationale: potassium (K) is a major component of several silicate minerals and seawater, and, therefore, constraining past changes in the potassium cycle is a promising way of tracing large-scale geological processes on Earth. However, [K] measurement using inductively coupled plasma mass spectrometry (ICP-MS) is challenging due to an ArH+ interference, which may be of a similar magnitude to the K+ ion beam in samples with <0.1% m/m [K].

Methods: in this work, we investigated the effect of the ArH+ interference on K/Ca data quality by comparing results from laser-ablation (LA)-ICP-MS measured in medium and high mass resolution modes and validating our LA results via solution ICP-optical emission spectroscopy (OES) and solution ICP-MS measurements. To do so, we used a wide range of geological reference materials, with a particular focus on marine carbonates, which are potential archives of past changes in the K cycle but are typically characterised by [K] < 200 μg/g. In addition, we examine the degree to which trace-element data quality is driven by downhole fractionation during LA-ICP-MS measurements.

Results: our results show that medium mass resolution (MR) mode is sufficiently capable of minimising the effect of the ArH+ interference on K+. However, the rate of downhole fractionation for Na and K varies between different samples as a result of their differing bulk composition, resulting in matrix-specific inaccuracy. We show how this can be accounted for via downhole fractionation corrections, resulting in an accuracy of better than 1% and a long-term reproducibility (intermediate precision) of <6% (relative standard deviation) in JCp-1NP using LA-ICP-MS in MR mode.

Conclusion: our [K] measurement protocol is demonstrably precise and accurate and applicable to a wide range of materials. The measurement of K/Ca in relatively low-[K] marine carbonates is presented here as a key example of a new application opened up by these advances.

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Accepted/In Press date: 6 December 2023
e-pub ahead of print date: 15 January 2024
Published date: 15 March 2024

Identifiers

Local EPrints ID: 503559
URI: http://eprints.soton.ac.uk/id/eprint/503559
ISSN: 0951-4198
PURE UUID: d5184642-1542-459d-9fa8-7a95d40beb24
ORCID for Romi Nambiar: ORCID iD orcid.org/0000-0003-4595-2630
ORCID for David Evans: ORCID iD orcid.org/0000-0002-8685-671X

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Date deposited: 05 Aug 2025 16:42
Last modified: 22 Aug 2025 02:46

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Contributors

Author: Romi Nambiar ORCID iD
Author: Jorit F. Kniest
Author: Alexander Schmidt
Author: Jacek Raddatz
Author: Wolfgang Müller
Author: David Evans ORCID iD

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