Low-δ18O (−8 ‰, VSMOW) Paleoproterozoic and discordant zircon: Lessons learned from using a combination of traditional bulk and in situ approaches

IF 3.6 2区 地球科学 Q1 GEOCHEMISTRY & GEOPHYSICS
David Zakharov, André Navin Paul, Dylan P. Colòn, Maria Ovtcharova, Benita Putlitz, Anne-Sophie Bouvier, Afrid Abdaly Sheik, Dmitry Zozulya, Martin Robyr
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引用次数: 0

Abstract

Zircon has become an important archive of early Earth's history relating the surface water cycle and magmatism via its O isotope composition. However, metamictization of zircon presents a challenge when dealing with ancient detrital grains that are removed from their host rock. Here we use an extremely low-δ18O zircon (−8 ‰) that is collected from an intact low-δ18O host rock in order to refine our analytical approaches to O isotope and UPb determinations. The δ18O of the hosting quartz is −4.2 ± 0.4 ‰, attesting to the primary nature of low δ18O values from an ancient water-rock interaction that originated in the Neoarchean. Highly variable 18O/16O of the zircon correlate positively with 16O1H/16O measured by SIMS, representing secondary hydration accompanied by O isotope exchange, from the least altered δ18O = −8.0 ± 0.1 ‰ to the highly hydrated domains with δ18O around +2 ‰. Previously measured near-concordant in situ UPb ages accompanied by high U (up to 0.5 wt%) present a puzzling observation of a preserved UPb system and highly disturbed O isotope compositions. Here we test the accuracy of these interpretations by combining several “gold standard” techniques including elemental X-ray mapping, bulk laser fluorination (δ18O), and chemical abrasion isotope dilution thermal ionization mass spectrometry (CA-ID-TIMS) for UPb ages. The zircon bulk δ18O values (−5.7 ‰ to −3.6 ‰) agree with the average values measured by SIMS, corroborating the effect of chemical removal of damaged domains by bulk that approach values in domains with low 16O1H/16O. Further, the triple O isotope compositions of zircon and quartz measured by laser fluorination have values similar to the isotope composition of the low-δ18O protoliths found within the same area. The δD value of −175 ‰ measured in a bulk zircon with 2.4 wt% H2O points to a near-surface source of hydrating waters. The CA-ID-TIMS UPb dating of such highly metamict zircon is challenged by almost complete loss of the analyte during the chemical abrasion step and by UPb discordant ages. Leaching at 130–210 °C for 3–12 h produces variably discordant ages, with one zircon grain yielding concordance and the 207Pb206Pb age of 1773 ± 2 Ma after leaching at 170 °C for 12 h, whereas leaching at higher temperature for less time produced inferior concordance. Both normal and reverse discordance are observed, indicating high and near-contemporaneous mobility of U/Pb. Here we document both major and trace elemental mobility that are mechanistically difficult to explain, however both are related to a fluid-zircon interaction and are only observable by a combination of in situ and bulk methods.
低δ 18o(- 8‰,VSMOW)古元古代与不和谐锆石:传统体法与原位法相结合的经验教训
锆石的O同位素组成已成为研究地球早期地表水循环和岩浆活动的重要档案。然而,锆石的变质作用在处理从其寄主岩石中移除的古代碎屑颗粒时提出了一个挑战。在这里,我们使用了从完整的低δ 18o寄主岩石中收集的极低δ 18o锆石(- 8‰),以改进我们的O同位素和UPb测定的分析方法。赋存石英的δ18O值为- 4.2 ± 0.4‰,表明其低δ18O值的主要成因是起源于新太古代的古水岩相互作用。锆石高变化的18O/16O与SIMS测得的16O1H/16O呈正相关,从δ18O变化最小的区域 = −8.0 ± 0.1‰到δ18O变化在+2‰左右的高度水化区域,体现了二次水化伴随O同位素交换。先前测量的近一致的原位UPb年龄伴随着高U(高达0.5 wt%),呈现出令人困惑的保存UPb系统和高度扰动的O同位素组成的观察结果。在这里,我们通过结合几种“金标准”技术来测试这些解释的准确性,这些技术包括元素x射线测绘、体激光氟化(δ18O)和化学磨损同位素稀释热电离质谱(CA-ID-TIMS)。锆石体积δ18O值(−5.7‰~−3.6‰)与SIMS测量的平均值吻合,证实了锆石体积化学去除损伤区域的效果,接近低16O1H/16O区域的数值。此外,激光氟化测量的锆石和石英的三O同位素组成与同一地区发现的低δ 18o原岩的同位素组成值相似。2.4 wt% H2O的块状锆石δD值为- 175‰,表明其为近地表水合水源。这种高变质锆石的CA-ID-TIMS UPb定年受到化学磨损过程中分析物几乎完全丢失和UPb年龄不一致的挑战。在130-210 °C条件下浸出3-12 h,产生的锆石年龄差异很大,在170 °C条件下浸出12 h,产生的锆石年龄为1773 ± 2 Ma,而在较高温度条件下浸出时间较短,产生的锆石年龄不一致。正常和反向不一致都被观察到,表明U/Pb的高迁移率和近同期的迁移率。在这里,我们记录了主要元素和痕量元素的迁移率,这些迁移率在机械上难以解释,但它们都与流体-锆石相互作用有关,并且只能通过原位和大块方法的结合来观察。
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来源期刊
Chemical Geology
Chemical Geology 地学-地球化学与地球物理
CiteScore
7.20
自引率
10.30%
发文量
374
审稿时长
3.6 months
期刊介绍: Chemical Geology is an international journal that publishes original research papers on isotopic and elemental geochemistry, geochronology and cosmochemistry. The Journal focuses on chemical processes in igneous, metamorphic, and sedimentary petrology, low- and high-temperature aqueous solutions, biogeochemistry, the environment and cosmochemistry. Papers that are field, experimentally, or computationally based are appropriate if they are of broad international interest. The Journal generally does not publish papers that are primarily of regional or local interest, or which are primarily focused on remediation and applied geochemistry. The Journal also welcomes innovative papers dealing with significant analytical advances that are of wide interest in the community and extend significantly beyond the scope of what would be included in the methods section of a standard research paper.
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