Boriana Kalderon-Asael, Jiuyuan Wang, Noah J. Planavsky, Amanda M. Oehlert, Brooke E. Vitek, R. Pamela Reid, Lidya G. Tarhan
{"title":"Evaluation of early diagenetic signatures of lithium and stable strontium isotopes in shallow marine carbonate sediments","authors":"Boriana Kalderon-Asael, Jiuyuan Wang, Noah J. Planavsky, Amanda M. Oehlert, Brooke E. Vitek, R. Pamela Reid, Lidya G. Tarhan","doi":"10.1016/j.chemgeo.2024.122590","DOIUrl":null,"url":null,"abstract":"Lithium (δ<ce:sup loc=\"post\">7</ce:sup>Li) and stable strontium isotope (δ<ce:sup loc=\"post\">88/86</ce:sup>Sr) ratios of shallow marine carbonate sediments serve as valuable proxies for reconstructing both seawater δ<ce:sup loc=\"post\">7</ce:sup>Li and δ<ce:sup loc=\"post\">88/86</ce:sup>Sr behavior and diverse geological processes. However, interpretations of these isotope values can be complicated by diagenesis. We conducted mineralogical, petrographic, and geochemical analyses of different sediment size fractions from two cores collected from distinct shallow marine depositional settings in the Bahamas, with the aim of evaluating the impact of early diagenetic processes on shallow water carbonate δ<ce:sup loc=\"post\">7</ce:sup>Li and δ<ce:sup loc=\"post\">88/86</ce:sup>Sr values. We found that the finest grain size fraction (i.e., < 63 μm or mud) is particularly vulnerable to recrystallization, leading to notable alteration of both δ<ce:sup loc=\"post\">7</ce:sup>Li and δ<ce:sup loc=\"post\">88/86</ce:sup>Sr values of mud-sized sediments relative to bulk sediment composition and expected fractionations from seawater. We interpret these data to reflect greater extents of recrystallization and secondary carbonate formation in the mud-sized fraction, linked to higher surface area to volume ratios. Although the alteration of the mud fraction appears to have minimally impacted bulk-sediment δ<ce:sup loc=\"post\">88/86</ce:sup>Sr or δ<ce:sup loc=\"post\">7</ce:sup>Li values, these findings expand the framework for interpreting the δ<ce:sup loc=\"post\">7</ce:sup>Li and δ<ce:sup loc=\"post\">88/86</ce:sup>Sr values of carbonate sediments.","PeriodicalId":9847,"journal":{"name":"Chemical Geology","volume":"51 1","pages":""},"PeriodicalIF":3.6000,"publicationDate":"2024-12-30","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.2024.122590","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
Lithium (δ7Li) and stable strontium isotope (δ88/86Sr) ratios of shallow marine carbonate sediments serve as valuable proxies for reconstructing both seawater δ7Li and δ88/86Sr behavior and diverse geological processes. However, interpretations of these isotope values can be complicated by diagenesis. We conducted mineralogical, petrographic, and geochemical analyses of different sediment size fractions from two cores collected from distinct shallow marine depositional settings in the Bahamas, with the aim of evaluating the impact of early diagenetic processes on shallow water carbonate δ7Li and δ88/86Sr values. We found that the finest grain size fraction (i.e., < 63 μm or mud) is particularly vulnerable to recrystallization, leading to notable alteration of both δ7Li and δ88/86Sr values of mud-sized sediments relative to bulk sediment composition and expected fractionations from seawater. We interpret these data to reflect greater extents of recrystallization and secondary carbonate formation in the mud-sized fraction, linked to higher surface area to volume ratios. Although the alteration of the mud fraction appears to have minimally impacted bulk-sediment δ88/86Sr or δ7Li values, these findings expand the framework for interpreting the δ7Li and δ88/86Sr values of carbonate sediments.
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.