David Zakharov, André Navin Paul, Dylan P. Colòn, Maria Ovtcharova, Benita Putlitz, Anne-Sophie Bouvier, Afrid Abdaly Sheik, Dmitry Zozulya, Martin Robyr
{"title":"Low-δ18O (−8 ‰, VSMOW) Paleoproterozoic and discordant zircon: Lessons learned from using a combination of traditional bulk and in situ approaches","authors":"David Zakharov, André Navin Paul, Dylan P. Colòn, Maria Ovtcharova, Benita Putlitz, Anne-Sophie Bouvier, Afrid Abdaly Sheik, Dmitry Zozulya, Martin Robyr","doi":"10.1016/j.chemgeo.2025.122972","DOIUrl":null,"url":null,"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-δ<ce:sup loc=\"post\">18</ce:sup>O zircon (−8 ‰) that is collected from an intact low-δ<ce:sup loc=\"post\">18</ce:sup>O host rock in order to refine our analytical approaches to O isotope and U<ce:glyph name=\"sbnd\"></ce:glyph>Pb determinations. The δ<ce:sup loc=\"post\">18</ce:sup>O of the hosting quartz is −4.2 ± 0.4 ‰, attesting to the primary nature of low δ<ce:sup loc=\"post\">18</ce:sup>O values from an ancient water-rock interaction that originated in the Neoarchean. Highly variable <ce:sup loc=\"post\">18</ce:sup>O/<ce:sup loc=\"post\">16</ce:sup>O of the zircon correlate positively with <ce:sup loc=\"post\">16</ce:sup>O<ce:sup loc=\"post\">1</ce:sup>H/<ce:sup loc=\"post\">16</ce:sup>O measured by SIMS, representing secondary hydration accompanied by O isotope exchange, from the least altered δ<ce:sup loc=\"post\">18</ce:sup>O = −8.0 ± 0.1 ‰ to the highly hydrated domains with δ<ce:sup loc=\"post\">18</ce:sup>O around +2 ‰. Previously measured near-concordant in situ U<ce:glyph name=\"sbnd\"></ce:glyph>Pb ages accompanied by high U (up to 0.5 wt%) present a puzzling observation of a preserved U<ce:glyph name=\"sbnd\"></ce:glyph>Pb 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 (δ<ce:sup loc=\"post\">18</ce:sup>O), and chemical abrasion isotope dilution thermal ionization mass spectrometry (CA-ID-TIMS) for U<ce:glyph name=\"sbnd\"></ce:glyph>Pb ages. The zircon bulk δ<ce:sup loc=\"post\">18</ce:sup>O 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 <ce:sup loc=\"post\">16</ce:sup>O<ce:sup loc=\"post\">1</ce:sup>H/<ce:sup loc=\"post\">16</ce:sup>O. Further, the triple O isotope compositions of zircon and quartz measured by laser fluorination have values similar to the isotope composition of the low-δ<ce:sup loc=\"post\">18</ce:sup>O protoliths found within the same area. The δD value of −175 ‰ measured in a bulk zircon with 2.4 wt% H<ce:inf loc=\"post\">2</ce:inf>O points to a near-surface source of hydrating waters. The CA-ID-TIMS U<ce:glyph name=\"sbnd\"></ce:glyph>Pb dating of such highly metamict zircon is challenged by almost complete loss of the analyte during the chemical abrasion step and by U<ce:glyph name=\"sbnd\"></ce:glyph>Pb discordant ages. Leaching at 130–210 °C for 3–12 h produces variably discordant ages, with one zircon grain yielding concordance and the <ce:sup loc=\"post\">207</ce:sup>Pb<ce:glyph name=\"sbnd\"></ce:glyph><ce:sup loc=\"post\">206</ce:sup>Pb 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.","PeriodicalId":9847,"journal":{"name":"Chemical Geology","volume":"24 1","pages":""},"PeriodicalIF":3.6000,"publicationDate":"2025-07-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Chemical Geology","FirstCategoryId":"89","ListUrlMain":"https://doi.org/10.1016/j.chemgeo.2025.122972","RegionNum":2,"RegionCategory":"地球科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"GEOCHEMISTRY & GEOPHYSICS","Score":null,"Total":0}
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.
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.