The use of Pb isotope ratios determined by magnetic sector ICP-MS for tracing Pb pollution in marine sediments near Casey Station, East Antarctica

Magnetic sector inductively coupled plasma mass spectrometry (ICP-SMS) was used to measure lead concentrations and isotope ratios in marine sediments and other samples collected from near the Australian Antarctic Station Casey. Precisions obtained from the repetitive analysis of a standard Broken Hi...

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Published in:Journal of Analytical Atomic Spectrometry
Main Authors: Townsend, AT, Snape, I
Format: Article in Journal/Newspaper
Language:English
Published: 2002
Subjects:
Online Access:https://eprints.utas.edu.au/565/
https://eprints.utas.edu.au/565/1/02_Casey_Pb_IRs_JAAS.pdf
https://doi.org/10.1039/b203449m
id ftunivtasmania:oai:eprints.utas.edu.au:565
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spelling ftunivtasmania:oai:eprints.utas.edu.au:565 2023-05-15T13:42:41+02:00 The use of Pb isotope ratios determined by magnetic sector ICP-MS for tracing Pb pollution in marine sediments near Casey Station, East Antarctica Townsend, AT Snape, I 2002 application/pdf https://eprints.utas.edu.au/565/ https://eprints.utas.edu.au/565/1/02_Casey_Pb_IRs_JAAS.pdf https://doi.org/10.1039/b203449m en eng https://eprints.utas.edu.au/565/1/02_Casey_Pb_IRs_JAAS.pdf Townsend, AT and Snape, I 2002 , 'The use of Pb isotope ratios determined by magnetic sector ICP-MS for tracing Pb pollution in marine sediments near Casey Station, East Antarctica' , Journal of Analytical Atomic Spectrometry, vol. 17 , pp. 922-928 , doi:10.1039/b203449m <http://dx.doi.org/10.1039/b203449m>. cc_utas 259902 Environmental Chemistry (incl. Atmospheric Chemistry) Article PeerReviewed 2002 ftunivtasmania https://doi.org/10.1039/b203449m 2020-05-30T07:14:19Z Magnetic sector inductively coupled plasma mass spectrometry (ICP-SMS) was used to measure lead concentrations and isotope ratios in marine sediments and other samples collected from near the Australian Antarctic Station Casey. Precisions obtained from the repetitive analysis of a standard Broken Hill Pb sample at a concentration of approximately 40 ng g-1 in solution were less than plus or minus 0.2% for ratios involving 204Pb, and less than plus or minus 0.1% for those referenced to 206Pb or 207Pb (n ~ 12 replicates over 2 days, values as 1s). Ratios were accurate to within less than plus or minus 0.1% for the analysis of this standard sample. Comparative measurements between ICP-SMS and TIMS had typical differences in values of less than 0.4% for contaminated samples, irrespective of ratio. For marine sediment samples with Pb concentrations in the sample digest of greater than 10 ng g-1, instrumental capability was characterised by isotopic precisions ranging from 0.1-0.5% (1s) for ratios involving 204Pb, and less than 0.25% (1s) for ratios with 206Pb or 207Pb as the basis (typically found from triplicate analyses). For sediments of low Pb concentration (less than 10 ng g-1 in the sample digest), isotope ratios to 204Pb were found to be limited by instrument counting statistics when using standard ICP-SMS. To help overcome this problem, Pb isotope ratios for these samples were measured with a capacitive decoupling Pt guard electrode employed, offering considerable signal enhancement (5-10x). These natural background sediments were found to display typical Pb isotope ratios of 40.5, 15.5, 18.6 and 1.19 for 208Pb/204Pb, 207Pb/204Pb, 206Pb/204Pb and 206Pb/207Pb. For comparison, the most contaminated samples had Pb isotope ratios of approximately 36.2, 15.4, 16.4 and 1.06 for 208Pb/204Pb, 207Pb/204Pb, 206Pb/204Pb and 206Pb/207Pb, respectively. Evidence of simple two component mixing between anthropogenic and natural geogenic Pb was found near Casey Station. Runoff from the Thala Valley tip site, adjacent to the bay, was identified as a clear source of Pb pollution, with impacted sediments displaying an isotopic signature approaching that of abandoned lead batteries collected from the tip. These batteries possessed Pb isotope ratios identical to Australian Broken Hill lead. In this study, the use of Pb isotope data has proved to be a sensitive method of assessing contamination levels in the Antarctic marine environment adjacent to a waste disposal site. Lead isotope ratios have proved superior to simple elemental concentration determinations when distinguishing between impacted and non-impacted samples. ICP-SMS has been shown to offer relatively fast, accurate and cost effective Pb isotope ratios, with precisions suitable for many environmental applications. Article in Journal/Newspaper Antarc* Antarctic Antarctica Antarctica Journal East Antarctica University of Tasmania: UTas ePrints Antarctic The Antarctic East Antarctica Casey Station ENVELOPE(110.528,110.528,-66.282,-66.282) Thala Valley ENVELOPE(110.536,110.536,-66.280,-66.280) Journal of Analytical Atomic Spectrometry 17 8 922 928
institution Open Polar
collection University of Tasmania: UTas ePrints
op_collection_id ftunivtasmania
language English
topic 259902 Environmental Chemistry (incl. Atmospheric Chemistry)
spellingShingle 259902 Environmental Chemistry (incl. Atmospheric Chemistry)
Townsend, AT
Snape, I
The use of Pb isotope ratios determined by magnetic sector ICP-MS for tracing Pb pollution in marine sediments near Casey Station, East Antarctica
topic_facet 259902 Environmental Chemistry (incl. Atmospheric Chemistry)
description Magnetic sector inductively coupled plasma mass spectrometry (ICP-SMS) was used to measure lead concentrations and isotope ratios in marine sediments and other samples collected from near the Australian Antarctic Station Casey. Precisions obtained from the repetitive analysis of a standard Broken Hill Pb sample at a concentration of approximately 40 ng g-1 in solution were less than plus or minus 0.2% for ratios involving 204Pb, and less than plus or minus 0.1% for those referenced to 206Pb or 207Pb (n ~ 12 replicates over 2 days, values as 1s). Ratios were accurate to within less than plus or minus 0.1% for the analysis of this standard sample. Comparative measurements between ICP-SMS and TIMS had typical differences in values of less than 0.4% for contaminated samples, irrespective of ratio. For marine sediment samples with Pb concentrations in the sample digest of greater than 10 ng g-1, instrumental capability was characterised by isotopic precisions ranging from 0.1-0.5% (1s) for ratios involving 204Pb, and less than 0.25% (1s) for ratios with 206Pb or 207Pb as the basis (typically found from triplicate analyses). For sediments of low Pb concentration (less than 10 ng g-1 in the sample digest), isotope ratios to 204Pb were found to be limited by instrument counting statistics when using standard ICP-SMS. To help overcome this problem, Pb isotope ratios for these samples were measured with a capacitive decoupling Pt guard electrode employed, offering considerable signal enhancement (5-10x). These natural background sediments were found to display typical Pb isotope ratios of 40.5, 15.5, 18.6 and 1.19 for 208Pb/204Pb, 207Pb/204Pb, 206Pb/204Pb and 206Pb/207Pb. For comparison, the most contaminated samples had Pb isotope ratios of approximately 36.2, 15.4, 16.4 and 1.06 for 208Pb/204Pb, 207Pb/204Pb, 206Pb/204Pb and 206Pb/207Pb, respectively. Evidence of simple two component mixing between anthropogenic and natural geogenic Pb was found near Casey Station. Runoff from the Thala Valley tip site, adjacent to the bay, was identified as a clear source of Pb pollution, with impacted sediments displaying an isotopic signature approaching that of abandoned lead batteries collected from the tip. These batteries possessed Pb isotope ratios identical to Australian Broken Hill lead. In this study, the use of Pb isotope data has proved to be a sensitive method of assessing contamination levels in the Antarctic marine environment adjacent to a waste disposal site. Lead isotope ratios have proved superior to simple elemental concentration determinations when distinguishing between impacted and non-impacted samples. ICP-SMS has been shown to offer relatively fast, accurate and cost effective Pb isotope ratios, with precisions suitable for many environmental applications.
format Article in Journal/Newspaper
author Townsend, AT
Snape, I
author_facet Townsend, AT
Snape, I
author_sort Townsend, AT
title The use of Pb isotope ratios determined by magnetic sector ICP-MS for tracing Pb pollution in marine sediments near Casey Station, East Antarctica
title_short The use of Pb isotope ratios determined by magnetic sector ICP-MS for tracing Pb pollution in marine sediments near Casey Station, East Antarctica
title_full The use of Pb isotope ratios determined by magnetic sector ICP-MS for tracing Pb pollution in marine sediments near Casey Station, East Antarctica
title_fullStr The use of Pb isotope ratios determined by magnetic sector ICP-MS for tracing Pb pollution in marine sediments near Casey Station, East Antarctica
title_full_unstemmed The use of Pb isotope ratios determined by magnetic sector ICP-MS for tracing Pb pollution in marine sediments near Casey Station, East Antarctica
title_sort use of pb isotope ratios determined by magnetic sector icp-ms for tracing pb pollution in marine sediments near casey station, east antarctica
publishDate 2002
url https://eprints.utas.edu.au/565/
https://eprints.utas.edu.au/565/1/02_Casey_Pb_IRs_JAAS.pdf
https://doi.org/10.1039/b203449m
long_lat ENVELOPE(110.528,110.528,-66.282,-66.282)
ENVELOPE(110.536,110.536,-66.280,-66.280)
geographic Antarctic
The Antarctic
East Antarctica
Casey Station
Thala Valley
geographic_facet Antarctic
The Antarctic
East Antarctica
Casey Station
Thala Valley
genre Antarc*
Antarctic
Antarctica
Antarctica Journal
East Antarctica
genre_facet Antarc*
Antarctic
Antarctica
Antarctica Journal
East Antarctica
op_relation https://eprints.utas.edu.au/565/1/02_Casey_Pb_IRs_JAAS.pdf
Townsend, AT and Snape, I 2002 , 'The use of Pb isotope ratios determined by magnetic sector ICP-MS for tracing Pb pollution in marine sediments near Casey Station, East Antarctica' , Journal of Analytical Atomic Spectrometry, vol. 17 , pp. 922-928 , doi:10.1039/b203449m <http://dx.doi.org/10.1039/b203449m>.
op_rights cc_utas
op_doi https://doi.org/10.1039/b203449m
container_title Journal of Analytical Atomic Spectrometry
container_volume 17
container_issue 8
container_start_page 922
op_container_end_page 928
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