{"title":"海洋埋藏成因过程中浅水碳酸盐硼同位素值的重置","authors":"Mingyu Zhao, B. Beaty, L. Tarhan, Noah Planavsky","doi":"10.2475/001c.91398","DOIUrl":null,"url":null,"abstract":"The boron isotopic composition (δ11B) of bulk carbonates may provide an archive to reconstruct changes in ocean pH. Reconstructions from ancient carbonates typically assume that no significant resetting of δ11B occurred during marine burial diagenesis. However, our understanding of B isotopic behavior associated with this process remains limited. Here we provide measurements of B/Ca and B isotopic composition (δ11B) from a modern peri-platform carbonate sequence near the Great Bahama Bank that has undergone marine burial diagenesis. Our results reveal significant decreases in both δ11B (~13 ‰) and B/Ca (~80 %) of bulk carbonates with depth. We attribute this pattern to the release of isotopically light B (δ11B ~20 ‰) to porewater during aragonite dissolution, with uptake of substantially isotopically lighter borate ions (δ11B ~-1 ‰) from porewater by newly forming low-Mg calcite. A quantitative model adds further support for this interpretation and provides an estimate of average neomorphism rate ( k0) in the range of 1×10-6 to 5×10-6 yr-1, which is comparable to previous rate estimates for neomorphism and/or recrystallization during meteoric diagenesis. Our results demonstrate the strong potential for resetting δ11B signatures in bulk carbonates during recrystallization, which must be considered in future attempts to reconstruct pH and pCO2 from these records and may require reinterpretation of existing records. Our results also suggest the potential of B isotopes as a proxy for carbonate recrystallization/neomorphism and original carbonate mineralogy.","PeriodicalId":7660,"journal":{"name":"American Journal of Science","volume":null,"pages":null},"PeriodicalIF":1.9000,"publicationDate":"2024-01-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Resetting of Shallow-Water Carbonate Boron Isotope Values During Marine Burial Diagenesis\",\"authors\":\"Mingyu Zhao, B. Beaty, L. Tarhan, Noah Planavsky\",\"doi\":\"10.2475/001c.91398\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"The boron isotopic composition (δ11B) of bulk carbonates may provide an archive to reconstruct changes in ocean pH. Reconstructions from ancient carbonates typically assume that no significant resetting of δ11B occurred during marine burial diagenesis. However, our understanding of B isotopic behavior associated with this process remains limited. Here we provide measurements of B/Ca and B isotopic composition (δ11B) from a modern peri-platform carbonate sequence near the Great Bahama Bank that has undergone marine burial diagenesis. Our results reveal significant decreases in both δ11B (~13 ‰) and B/Ca (~80 %) of bulk carbonates with depth. We attribute this pattern to the release of isotopically light B (δ11B ~20 ‰) to porewater during aragonite dissolution, with uptake of substantially isotopically lighter borate ions (δ11B ~-1 ‰) from porewater by newly forming low-Mg calcite. A quantitative model adds further support for this interpretation and provides an estimate of average neomorphism rate ( k0) in the range of 1×10-6 to 5×10-6 yr-1, which is comparable to previous rate estimates for neomorphism and/or recrystallization during meteoric diagenesis. Our results demonstrate the strong potential for resetting δ11B signatures in bulk carbonates during recrystallization, which must be considered in future attempts to reconstruct pH and pCO2 from these records and may require reinterpretation of existing records. Our results also suggest the potential of B isotopes as a proxy for carbonate recrystallization/neomorphism and original carbonate mineralogy.\",\"PeriodicalId\":7660,\"journal\":{\"name\":\"American Journal of Science\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":1.9000,\"publicationDate\":\"2024-01-09\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"American Journal of Science\",\"FirstCategoryId\":\"89\",\"ListUrlMain\":\"https://doi.org/10.2475/001c.91398\",\"RegionNum\":3,\"RegionCategory\":\"地球科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"GEOSCIENCES, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"American Journal of Science","FirstCategoryId":"89","ListUrlMain":"https://doi.org/10.2475/001c.91398","RegionNum":3,"RegionCategory":"地球科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"GEOSCIENCES, MULTIDISCIPLINARY","Score":null,"Total":0}
Resetting of Shallow-Water Carbonate Boron Isotope Values During Marine Burial Diagenesis
The boron isotopic composition (δ11B) of bulk carbonates may provide an archive to reconstruct changes in ocean pH. Reconstructions from ancient carbonates typically assume that no significant resetting of δ11B occurred during marine burial diagenesis. However, our understanding of B isotopic behavior associated with this process remains limited. Here we provide measurements of B/Ca and B isotopic composition (δ11B) from a modern peri-platform carbonate sequence near the Great Bahama Bank that has undergone marine burial diagenesis. Our results reveal significant decreases in both δ11B (~13 ‰) and B/Ca (~80 %) of bulk carbonates with depth. We attribute this pattern to the release of isotopically light B (δ11B ~20 ‰) to porewater during aragonite dissolution, with uptake of substantially isotopically lighter borate ions (δ11B ~-1 ‰) from porewater by newly forming low-Mg calcite. A quantitative model adds further support for this interpretation and provides an estimate of average neomorphism rate ( k0) in the range of 1×10-6 to 5×10-6 yr-1, which is comparable to previous rate estimates for neomorphism and/or recrystallization during meteoric diagenesis. Our results demonstrate the strong potential for resetting δ11B signatures in bulk carbonates during recrystallization, which must be considered in future attempts to reconstruct pH and pCO2 from these records and may require reinterpretation of existing records. Our results also suggest the potential of B isotopes as a proxy for carbonate recrystallization/neomorphism and original carbonate mineralogy.
期刊介绍:
The American Journal of Science (AJS), founded in 1818 by Benjamin Silliman, is the oldest scientific journal in the United States that has been published continuously. The Journal is devoted to geology and related sciences and publishes articles from around the world presenting results of major research from all earth sciences. Readers are primarily earth scientists in academia and government institutions.