Geochronological and geochemical effects of zircon chemical abrasion: insights from single-crystal stepwise dissolution experiments

IF 2.7 Q2 GEOCHEMISTRY & GEOPHYSICS
A. McKanna, B. Schoene, D. Szymanowski
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引用次数: 1

Abstract

Abstract. Chemical abrasion in hydrofluoric acid (HF) is routinely applied to zircon grains prior to U–Pb dating by isotope dilution thermal ionization mass spectrometry (ID-TIMS) to remove radiation-damaged portions of grains affected by Pb loss. Still, many chemically abraded datasets exhibit evidence of residual Pb loss. Here we test how the temperature and duration of chemical abrasion affect zircon U–Pb and trace element systematics in a series of 4 h, single-crystal stepwise dissolution experiments at 180 and 210 ∘C. Microtextural data for the zircon samples studied are presented in a companion paper by McKanna et al. (2023). We find that stepwise dissolution at 210 ∘C is more effective at eliminating material affected by open-system behavior and enriched in U, common Pb (Pbc), and light rare earth elements (LREEs); reduces the presence of leaching-induced artifacts that manifest as reverse discordance; and produces more consistent and concordant results in zircon from the three rocks studied. We estimate that stepwise dissolution in three 4 h steps is roughly equivalent to a single ∼ 8 h leaching step due to the insulating properties of the PTFE sleeve in the Parr pressure dissolution vessel, whereas traditionally labs utilize a single 12 h leaching step. We conclude that a single 8 h leaching step at 210 ∘C should remove Pb loss effects in the majority of zircon and that this can be used as an effective approach for routine analysis. Further, we calculate time-integrated alpha doses for leachates and residues from measured radionuclide concentrations to investigate (1) the alpha dose of the material dissolved under the two leaching conditions and (2) the apparent minimum alpha dose required for Pb loss susceptibility: ≥ 6×1017 α g−1.
锆石化学磨损的地质年代和地球化学效应:单晶逐步溶解实验的启示
摘要。在采用同位素稀释热电离质谱法(ID-TIMS)对锆石晶粒进行 U-Pb 测定之前,通常会在氢氟酸(HF)中对其进行化学研磨,以去除晶粒中受辐射损伤的铅损失部分。尽管如此,许多化学研磨数据集仍显示出残余铅损失的证据。在此,我们在 180 和 210 ∘C下进行了一系列 4 小时的单晶逐步溶解实验,测试了化学研磨的温度和持续时间如何影响锆石的 U-Pb 和痕量元素系统学。所研究的锆石样品的微纹理数据见 McKanna 等人的论文(2023 年)。我们发现,在 210 ∘C 下逐步溶解能更有效地剔除受开放系统行为影响、富含铀、普通铅 (Pbc) 和轻稀土元素 (LREE) 的物质;减少表现为反向不一致性的浸出诱导假象的存在;并对所研究的三种岩石中的锆石得出更一致、更协调的结果。我们估计,由于帕尔压力溶解容器中聚四氟乙烯套筒的绝缘性能,分三个 4 小时步骤进行的逐步溶解大致相当于一个 8 小时的浸出步骤,而传统实验室采用的是一个 12 小时的浸出步骤。我们的结论是,在 210 ∘C 温度下进行 8 小时的单次浸出步骤应能消除大多数锆石的铅损失效应,这可作为常规分析的有效方法。此外,我们还根据测得的放射性核素浓度计算了浸出液和残留物的时间积分α剂量,以研究:(1)两种浸出条件下溶解物质的α剂量;(2)铅流失敏感性所需的最小α剂量:≥ 6×1017 α g-1。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Geochronology
Geochronology Earth and Planetary Sciences-Paleontology
CiteScore
6.60
自引率
0.00%
发文量
35
审稿时长
19 weeks
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